CN1104410C - 苯乙酸衍生物及其制备和中间体以及含有它们的组合物 - Google Patents
苯乙酸衍生物及其制备和中间体以及含有它们的组合物 Download PDFInfo
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- CN1104410C CN1104410C CN95191969A CN95191969A CN1104410C CN 1104410 C CN1104410 C CN 1104410C CN 95191969 A CN95191969 A CN 95191969A CN 95191969 A CN95191969 A CN 95191969A CN 1104410 C CN1104410 C CN 1104410C
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- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/30—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
- C07D207/32—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C07D207/33—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms with substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C07D207/333—Radicals substituted by oxygen or sulfur atoms
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- A01N37/36—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C249/00—Preparation of compounds containing nitrogen atoms doubly-bound to a carbon skeleton
- C07C249/04—Preparation of compounds containing nitrogen atoms doubly-bound to a carbon skeleton of oximes
- C07C249/08—Preparation of compounds containing nitrogen atoms doubly-bound to a carbon skeleton of oximes by reaction of hydroxylamines with carbonyl compounds
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- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C251/00—Compounds containing nitrogen atoms doubly-bound to a carbon skeleton
- C07C251/32—Oximes
- C07C251/34—Oximes with oxygen atoms of oxyimino groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals
- C07C251/36—Oximes with oxygen atoms of oxyimino groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals with the carbon atoms of the oxyimino groups bound to hydrogen atoms or to acyclic carbon atoms
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- C07C251/32—Oximes
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- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
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- C07C327/58—Derivatives of thiocarboxylic acids, the doubly-bound oxygen atoms being replaced by nitrogen atoms, e.g. imino-thio ethers
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- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
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- C07C2601/14—The ring being saturated
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- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Thiazole And Isothizaole Compounds (AREA)
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- Heterocyclic Compounds Containing Sulfur Atoms (AREA)
- Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Quinoline Compounds (AREA)
- Indole Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Hydrogenated Pyridines (AREA)
Abstract
式I所示的苯乙酸衍生物及其盐,制备它们的方法和中间体,以及它们的用途,其中取代基和符号定义如下:X 为NOCH3,CHOCH3,CHCH3和〔SiC〕CHCH2CH3;R1 为氢和烷基;R2为氰基,硝基,三氟甲基,卤素,烷基和烷氧基m 为0,1或2,如果m为2,R2基团可以不同;R3为氢,氰基,硝基,羟基,氨基,卤素,烷基,卤代烷基,烷氧基,卤代烷氧基,烷硫基,烷氨基或双烷氨基;R4为氢,氰基,硝基,羟基,氨基,卤素,未取代或取代的烷基,烷氧基,烷硫基,烷氨基,双烷氨基,链烯基,链烯氧基,链烯硫基,链烯氨基,N-链烯基-N-烷基氨基,炔基,炔氧基,炔硫基,炔氨基,N-炔基-N-烷基氨基;未取代的或取代的环烷基,环烷氧基,环烷硫基,环烷氨基,N-环烷基-N-烷基氨基,环烯基,环烯氧基,环烯硫基,环烯氨基,N-环烯基-N-烷基氨基,杂环基,杂环氧基,杂环硫基,杂环氨基,N-杂环基-N-烷基氨基,芳基,芳氧基,芳硫基,芳氨基,N-芳基-N-烷基氨基,杂芳基,杂芳氧基,杂芳硫基,杂芳氨基,N-杂芳基-N-烷基氨基;R5为氢,未取代或取代的烷基,环烷基,链烯基,炔基,烷羰基,链烯羰基,炔羰基或烷基磺酰基,未取代或取代的芳基,芳羰基,芳基磺酰基,杂芳基,杂芳羰基或杂芳基磺酰基。
Description
本发明涉及式I的苯乙酸衍生物及其盐其中的取代基和符号定义如下:X 为NOCH3,CHOCH3,CHCH3和CHCH2CH3;R1 为氢和C1-C4-烷基;R2 为氰基,硝基,三氟甲基,卤素,C1-C4-烷基和C1-C4-烷氧
基;m 为0,1或2,如果m为2,R2可以是不同的基团;R3 为氢,氰基,硝基,羟基,氨基,卤素,C1-C4-烷基,C1-C4
-卤代烷基,C1-C4-烷氧基,C1-C4-卤代烷氧基,C1-C4
-烷硫基,C1-C4-烷氨基或双-C1-C4-烷基氨基;R4 为氢,氰基,硝基,羟基,氨基,卤素,C1-C6-烷基,C1-C6
-烷氧基,C1-C6-烷硫基,C1-C6-烷氨基,双-C1-C6
-烷基氨基,C2-C6-链烯基,C2-C6-链烯氧基,C2-C6
-链烯硫基,C2-C6-链烯氨基,N-C2-C6-链烯基-N-
C1-C6-烷基氨基,C2-C6-链炔基,C2-C6-链炔氧基,
C2-C6-链炔硫基,C2-C6-链炔氨基,N-C2-C6-链炔
基-N-C1-C6-烷基氨基,这些基团中的烃基可被部分或完全
卤代或带有一到三个下列基团:氰基,硝基,羟基,巯基,氨基,羧基,氨羰基,氨基硫代羰基,卤素,C1-C6-烷氨基羰基,双-C1-C6-烷基氨基羰基,C1-C6-烷氨基硫代羰基,双-C1-C6-烷基氨基硫代羰基,C1-C6-烷基磺酰基,C1-C6烷基亚磺酰基(C1-C6-alkylsulfoxyl),C1-C6-烷氧基,C1-C6-卤代烷氧基,C1-C6-烷氧羰基,C1-C6-烷硫基,C1-C6-烷氨基,双-C1-C6-烷基氨基,C2-C6链烯氧基,C3-C6-环烷基,C3-C6-环烷氧基,杂环基,杂环氧基,芳基,芳氧基,芳基-C1-C4-烷氧基,芳硫基,芳基-C1-C4-烷硫基,杂芳基,杂芳氧基,杂芳基-C1-C4-烷氧基,杂芳硫基,杂芳基-C1-C4-烷硫基,而其中的环状基团又可被部分或完全卤代和/或带有一到三个下列基团:氰基,硝基,羟基,巯基,氨基,羧基,氨羰基,氨硫代羰基,C1-C6烷基,C1-C6-卤代烷基,C1-C6-烷基磺酰基,C1-C6-烷基亚磺酰基,C3-C6-环烷基,C1-C6-烷氧基,C1-C6-卤代烷氧基,C1-C6-烷氧羰基,C1-C6-烷硫基,C1-C6-烷氨基,双-C1-C6-烷基氨基,C1-C6-烷氨基羰基,双-C1-C6-烷基氨基羰基,C1-C6-烷氨基硫代羰基,双-C1-C6-烷基氨基硫代羰基,C2-C6-链烯基,C2-C6-链烯氧基,苄基,苄氧基,芳基,芳氧基,芳硫基,杂芳基,杂芳氧基,杂芳硫基,和C(=NOR6)-An-R7;C3-C6-环烷基,C3-C6-环烷氧基,C3-C6-环烷硫基,C3-C6-环烷氨基,N-C3-C6-环烷基-N-C1-C6-烷基氨基,C3-C6-环烯基,C3-C6-环烯氧基,C3-C6-环烯硫基,C3-C6-环烯氨基,N-C3-C6-环烯基-N-C1-C6-烷基氨基,杂环基,杂环氧基,杂环硫基,杂环氨基,N-杂环基-N-C1-C6-烷基氨基,芳基,芳氧基,芳硫基,芳氨基,N-芳基-N-C1-C6-烷基氨基,杂芳基,杂芳氧基,杂芳硫基,杂芳氨基,N-杂芳基-N-C1-C6-烷基氨基,其中的环状基团可被部分或完全卤代或带有一到三个下列基团:氰基,硝基,羟基,巯基,氨基,羧基,氨羰基,氨硫代羰基,卤素,
C1-C6-烷基,C1-C6-卤代烷基,C1-C6-烷基磺酰基,
C1-C6-烷基亚磺酰基,C3-C6-环烷基,C1-C6-烷氧基,
C1-C6-卤代烷氧基,C1-C6-烷氧羰基,C1-C6-烷硫基,
C1-C6-烷氨基,双-C1-C6-烷基氨基,C1-C6-烷氨基羰
基,双-C1-C6-烷基氨基羰基,C1-C6-烷氨基硫代羰基,
双-C1-C6-烷基氨基硫代羰基,C2-C6-链烯基,C2-C6
-链烯氧基,苄基,苄氧基,芳基,芳氧基,杂芳基和杂芳氧基;R5 为氢,
C1-C10-烷基,C3-C6-环烷基,C2-C10-链烯基,C2-
C10-链炔基,C1-C10-烷羰基,C2-C10-链烯羰基,C3-
C10-链炔羰基或C1-C10-烷基磺酰基,这些基团可被部分或完
全卤代或带有一到三个下列基团:氰基,硝基,羟基,巯基,氨基,
羧基,氨羰基,氨基硫代羰基,卤素,C1-C6-烷基,C1-C6
-卤代烷基,C1-C6-烷基磺酰基,C1-C6-烷基亚磺酰基,
C1-C6-烷氧基,C1-C6-卤代烷氧基,C1-C6-烷氧羰基,
C1-C6-烷硫基,C1-C6-烷氨基,双-C1-C6-烷基氨基,
C1-C6-烷氨基羰基,双-C1-C6-烷基氨基羰基,C1-C6
-烷氨基硫代羰基,双-C1-C6-烷基氨基硫代羰基,C2-C6
-链烯基,C2-C6-链烯氧基,C3-C6-环烷基,C3-C6-
环烷氧基,杂环基,杂环氧基,苄基,苄氧基,芳基,芳氧基,芳
硫基,杂芳基,杂芳氧基和杂芳硫基,而这些基团中的环状基团又
可被部分或完全卤代或带有一到三个下列基团:氰基,硝基,羟基,
巯基,氨基,羧基,氨羰基,氨基硫代羰基,卤素,C1-C6-烷
基,C1-C6-卤代烷基,C1-C6-烷基磺酰基,C1-C6-烷基
亚磺酰基,C3-C6-环烷基,C1-C6-烷氧基,C1-C6-卤
代烷氧基,C1-C6-烷氧羰基,C1-C6-烷硫基,C1-C6-
烷氨基,双-C1-C6-烷基氨基,C1-C6-烷氨基羰基,双-
C1-C6-烷基氨基羰基,C1-C6-烷氨基硫代羰基,双-C1-
C6-烷基氨基硫代羰基,C2-C6-链烯基,C2-C6-链烯氧
基,苄基,苄氧基,芳基,芳氧基,芳硫基,杂芳基,杂芳氧基,
杂芳硫基,或C(=NOR6)-An-R7;
芳基,芳羰基,芳基磺酰基,杂芳基,杂芳基羰基或杂芳基磺酰基,
这些基团可被部分或完全卤代或带有一到三个下列基团:氰基,硝
基,羟基,巯基,氨基,羧基,氨基羰基,氨基硫代羰基,卤素,
C1-C6-烷基,C1-C6-卤代烷基,C1-C6-烷基羰基,C1
-C6-烷基磺酰基,C1-C6-烷基亚磺酰基,C3-C6-环烷基,C1
-C6-烷氧基,C1-C6-卤代烷氧基,C1-C6-烷氧羰基,C1-
C6-烷硫基,C1-C6-烷氨基,双-C1-C6-烷基氨基,C1-C6-
烷氨基羰基,双-C1-C6-烷基氨基羰基,C1-C6-烷氨基硫代羰
基,双-C1-C6-烷基氨基硫代羰基,C2-C6链烯基,C2-C6-
链烯氧基,苄基,苄氧基,芳基,芳氧基,杂芳基,杂芳氧基或
C(=NOR6)-An-R7;其中A 为氧、硫或氮,其中氮带有氢或C1-C6烷基;n 为0或1;R6 为氢或C1-C6-烷基,以及R7 为氢或C1-C6-烷基。
本发明还涉及制备这些化合物的方法和中间体以及含有它们的控制动物害虫和有害真菌的组合物。
苯乙酸衍生物对害虫的控制已公开于文献(EP-A 422597,EP-A463488,EP-A370629,EP-A460575,EP-A472300,WO-A90/07,493,WO-A 92/13,830,WO-A 92/18,487)中。
本发明的目的是提供新的具有更高活性的化合物。
我们发现可由开始定义的苯乙酸衍生物实现这个目的。我们还发现制备它们的方法和中间体以及含有它们的控制动物害虫和有害真菌的组合物和它们的用途。
化合物I可通过文献中已知的方法得到。
基本上,是首先形成基团-C(X)-CO2R1还是首先形成基团-CH2ON=(CR3)-C(R4)=NOR5在化合物I的合成中无关紧要。
基团-C(X)-CO2R1的合成例如公开了本文开始例举的文献中。
侧链-CH2ON=C(R3)-C(R4)=NOR5的合成方式主要取决于取代基R3和R4的性质。1.如果R3和R4不是卤素,基团-CH2ON=C(R3)-C(R4)=NOR5一般由通式II的苄基衍生物与式III的羟基亚胺的反应完成。式II中L1为可被亲核取代的离去基团,例如,卤素或磺酸酯基,优选氯、溴、碘、甲磺酸酯基、甲苯磺酸酯基或三氟甲磺酸酯基。反应按Houben-Weyl,Vol.E 14b,p.370ff和Houben-Weyl,Vol.10/1,p.1189ff所述的方法,在碱(例如氢化钠、氢氧化钾、碳酸钾和三乙胺)存在下,在惰性有机溶剂中,以本质已知的方式进行。所需的羟基亚胺III例如可由相应的二羟基亚胺IV与亲核取代试剂VI的反应得到
VI IV III式VI中L2为可被亲核取代的离去基团,例如卤素或磺酸酯基,优选氯、溴、碘、甲磺酸酯基、甲苯磺酸酯基或三氟甲磺酸酯基。该反应按Houben-Weyl,Vol.E 14b,p.307ff,p.370ff和p.385ff; Houben-Weyl,Vol.10/4,p.55ff,p.180ff和p.217ff;Houben-Weyl,Vol.E5,p780ff所述方法,在碱(例如碳酸钾、氢氧化钾、氢化钠、吡啶和三乙胺)存在下,在惰性有机溶剂中,以本质已知的方式进行。1.1选择性地,化合物I也可通过首先使用二羟基亚胺衍生物IV将苄基衍生物II转化成相应的式V苄基肟,然后使V与亲核取代试剂VI反应而得到。该反应可按Houben-Weyl,Vol.10/1,p.1189ff;Houben-Weyl,Vol.E 14b,p.307ff,p.370ff和p.385ff;Houben-Weyl,Vol.10/4,p.55ff,p.180ff和p.217ff;Houben-Weyl,Vol.E 5,p.780ff.所述的方法,在碱(例如碳酸钾、氢氧化钾、氢化钠、吡啶和三乙胺)的存在下,在惰性有机溶剂中,以本质已知的方式进行。1.2也可以相似的方式,通过与羟胺IXa或其盐IXb反应而由羰基羟基亚胺VII制备所需的式III羟基亚胺。
→R5-ON=C(R4)-C(R3)=NOH
III式IXb中Q-为酸、特别是无机酸的阴离子,例如卤离子,如氯离子。该反应可按EP-A513580;Houben-Weyl,Vol.19/4,p.73ff;Houben-Weyl,Vol.E 14b,p.369ff和p.385ff所述的方法,在惰性有机溶剂中,以本质已知的方式进行。1.3选择性地,化合物I也可通过首先使用羰基羟亚胺衍生物VII将苄基衍生物II转化成相应的式VIII苄氧基亚胺,然后使VIII与羟胺IXa或其盐IXb反应而得到。该反应按Houben-Weyl,Vol.E14b,p369ff,Houben-Weyl,Vol.10/1,p.1189ff和Houben-Weyl,Vol.10/4,p.73ff或EP-A513580所述的方法,在惰性有机溶剂中,以本质已知的方式进行。1.4另一种制备化合物I的可能方法是使苄基衍生物II与N-羟基苯邻二甲酰亚胺反应,然后肼解成苄基羟胺IIa,并使IIa进一步与羰基化合物X反应。
X该反应可按EP-A 463 488,DE-A4228867.3所述的方法、在惰性有机溶剂中,以本质已知的方式进行。所需的羰基化合物X例如可如下制备:通过相应的羟基亚胺基羰基化合物VIIa与亲核取代试剂VI反应
VI VIIa X或通过相应二羰基化合物XI与羟胺IXa或其盐IXb的反应
→R5-ON=C(R4)-C(R3)=O
X这些反应可按照EP-A513580,Houben-Weyl,Vol.10/4,p.55ff,p.73ff,p.180ff和p.217ff,Houben-Weyl,vol.E 14b,p.307ff和369ff,Houben-Weyl,Vol.E5,p.780ff。所描述的方法,在惰性有机溶剂中,以本质已知的方式进行。1.5相应地,上述化合物I也可通过首先使用羟基亚胺衍生物VIIa将苄基羟胺IIa转化成相应的式V苄氧基亚胺衍生物,然后再使V与亲核取代试剂VI反应而得到。1.6相似地,上述化合物I也可通过首先使用式XI二羰基衍生物将苄基羟胺IIa转化成苄氧基亚胺衍生物VIII,然后使VIII与羟胺IXa或其盐IXb反应得到。2.其中R3和/或R6为卤原子的化合物可由本质已知的方法、由其中有关基团为羟基的相应前体得到(cf.Houben-Weyl,Vol.E5,p.631;J.Org.Chem.36(1971),233;J.Org.Chem.57(1992),3245)。优选地,得到卤衍生物的相应的反应在步骤I和VIII中完成。3.其中R3和/或R4通过O、S或N连接于分子结构上的化合物可通过本质已知的方法由有关基团为卤原子的相应前体得到(cf.Houben-Weyl,Vol.E5,p.826ff和128ff,J.Org.Chem.36(1971),233,J.Org.Chem.46(1981),3623)。优选地,卤衍生物的相应的转化在步骤I和VIII中完成。4.其中R3和R4通过氧原子连接于分子上的化合物有时也可通过本质已知的方法由有关基团为羟基的相应前体得到(cf. Houben-Weyl,Vol.E5,p.826-829,Aust.J.Chem.
27(1974),1341-9)。优选地,得到烷氧基衍生物的相应反应在步骤I和VIII中完成。5.其中R3不为卤素的化合物优选地通过首先按EP-A 493711所述的方法使用内酯XII将化合物X转化为相应的苯甲酸XIII,并经相应的酰卤将XIII转化为氰代羧酸XIV,将其通过Pinner反应的方法(Angew.Chem.94(1982),1)转化为α-酮酯XV,然后再转化成衍生物I(cf.EP348766,DE 3705389,EP 178826,DE 3623921)。
其中R1为氢的化合物I按此方法通过水解酯XV和随后的反应而得到。
化合物II为已知物或可按文献所述的方法制备(EP-A513580,EP-A477631,EP-A463488,EP-A370629,EP-A460575)。
由于具有C=C和C=N双键,在制备过程中可得到E/Z异构体混合物,通过常规方法,例如,结晶和层析可将其分离成单纯化合物。
但是,合成中得到的异构体混合物并不一定需要分离,这是因为单纯异构体在制备时或应用时可在某些情况下相互转化(例如,在光、酸或碱的作用下)。相应的转化也可发生在施用之后,例如植物处理期在被处理的植物上或在被控制的有害真菌或动物害虫中。
对于C=X双键,考虑到它们的活性,优选化合物I的E异构体(取决于-CO2R1基团与-OCH3、-CH3或-CH2CH3基团的相互位置)
对于-C(R3)=NOCH2-双键,考虑到它们的活性,优选化合物I的顺式异构体(取决于R3与-OCH2-基团的相互位置)
在上文给出的化合物3的定义中使用的集合术语通常表示下列基团:卤素:氟,氯,溴和碘;烷基:具有1到4、6或10个碳原子的直链或支链烷基,例如C1-C6-烷基如甲基、乙基、丙基、1-甲基乙基、丁基、1-甲基丙基、2-甲基丙基、1,1-二甲基乙基、戊基、1-甲基丁基、2-甲基丁基、3-甲基丁基、2,2-二甲基丙基、1-乙基丙基、己基、1,1-二甲基丙基、1,2-二甲基丙基、1-甲基戊基、2-甲基戊基、3-甲基戊基、3-甲基戊基、4-甲基戊基、1,1-二甲基丁基、1,2-二甲基丁基、1,3-二甲基丁基、2,2-二甲基丁基、2,3-二甲基丁基、3,3-二甲基丁基、1-乙基丁基、2-乙基丁基、1,1,2-三甲基丙基、1,2,2-三甲基丙基、1-乙基-1-甲基丙基和1-乙基-2-甲基丙基;烷氨基:带有一个如上所述的具有1到6个碳原子的支链或支链烷基的氨基;双烷基氨基:带有相互独立的两个如上所述的具有1到6个碳原子的直链或支链烷基的氨基;烷羰基:经羰基(-CO-)与主结构相连的具有1到10个碳原子的直链或支链烷基;烷基磺酰基:经磺酰基(-SO2-)与主结构相连的具有1到6或10个碳原子的直链或支链烷基;烷基亚磺酰基:经亚磺酰基(-S(=O)-)与主结构相连的具有1到6个碳原子的直链或支链烷基;烷氨基羰基:经羰基(-CO-)与主结构相连的具有1-6个碳原子的上述烷氨基;双烷基氨基羰基:经羰基(-CO-)与主结构相连的上述双烷基氨基,其中每个烷基具有1到6个碳原子;烷氨基硫代羰基:经硫代羰基(-CS-)与主结构相连的具有1到6个碳原子的上述烷氨基。双烷基氨基硫代羰基:经硫代羰基(-CS-)与主结构相连的上述双烷基氨基,其中每个烷基具有1到6个碳原子;卤代烷基:具有1到6个碳原子的直链或支链烷基,这些基团上的氢原子可被上述卤原子部分或完全取代,例如C1-C2-卤代烷基,如氯甲基、二氯甲基、三氯甲基、氟甲基、二氟甲基、三氟甲基、氯氟甲基、二氯一氟甲基、一氯二氟甲基、1-氟乙基、2-氟乙基、2,2-二氟乙基、2,2,2-三氟乙基、2-氯-2-氟乙基、2-氯-2,2-二氟乙基、2,2-二氯-2-氟乙基、2,2,2-三氯乙基和五氟乙基;烷氧基:经氧原子(-O-)与主结构相连的具有1到4或6个碳原子的上述直链或支链烷基,例如C1-C6-烷氧基,如甲氧基、乙氧基、丙氧基、1-甲基乙氧基、丁氧基、1-甲基丙氧基、2-甲基丙氧基、1,1-二甲基乙氧基、戊氧基、1-甲基丁氧基、2-甲基丁氧基、3-甲基丁氧基、2,2-二甲基丙氧基、1-乙基丙氧基、己氧基、1,1-二甲基丙氧基、1,2-二甲基丙氧基、1-甲基戊氧基、2-甲基戊氧基、3-甲基戊氧基、4-甲基戊氧基、1,1-二甲基丁氧基、1,2-二甲基丁氧基、1,3-二甲基丁氧基、2,2-二甲基丁氧基、2,3-二甲基丁氧基、3,3-二甲基丁氧基、1-乙基丁氧基、2-乙基丁氧基、1,1,2-三甲基丙氧基、1,2,2-三甲基丙氧基、1-乙基-1-甲基丙氧基和1-乙基-2-甲基丙氧基;烷氧羰基:经氧羰基(-O(C=O)-)与主结构相连的具有1到6个碳原子的直链或支链烷基;卤代烷氧基:经氧原子与主结构相连的具有1到6个碳原子的直链或支链烷基,这些烷基中的氢原子可被上述卤原子部分或完全取代;烷硫基:经硫原子(-S-)与主结构相连的具有1到4或6个碳原子的上述直链或支链烷基,例如C1-C6-烷硫基,如甲硫基、乙硫基、丙硫基、1-甲基乙硫基、丁硫基、1-甲基丙硫基、2-甲基丙硫基、1,1-二甲基乙硫基、戊硫基、1-甲基丁硫基、2-甲基乙硫基、3-甲基丁硫基、2,2-二甲基丙硫基、1-乙基丙硫基、己硫基、1,1-二甲基丙硫基、1,2-二甲基丙硫基、1-甲基戊硫基、2-甲基戊硫基、3-甲基戊硫基、4-甲基戊硫基、1,1-二甲基丁硫、基,2-二甲基丁硫基、1,3-二甲基丁硫基、2,2-二甲基丁硫基、2,3-二甲基丁硫基、3,3-二甲基丁硫基、1-乙基丁硫基、2-乙基丁硫基、1,1,2-三甲基丙硫基、1,2,2,-三甲基丙硫基、1-乙基-1-甲基丙硫基和1-乙基-2-甲基丙硫基;环烷基:具有3到6个环碳原子的单环烷基,例如环丙基、环丁基、环戊基和环己基;链烯基:双键可在任何位置的具有2到6或10个碳原子的直链或支链链烯基,例如C2-C6-链烯基,如乙烯基、1-丙烯基、2-丙烯基、1-甲基乙烯基、1-丁烯基、2-丁烯基、3-丁烯基、1-甲基-1-丙烯基、2-甲基-1-丙烯基、1-甲基-2-丙烯基、2-甲基-2-丙烯基、1-戊烯基、2-戊烯基、3-戊烯基、4-戊烯基、1-甲基-1-丁烯基、2-甲基-1-丁烯基、3-甲基-1-丁烯基、1-甲基-2-丁烯基、2-甲基-2-丁烯基、3-甲基-2-丁烯基、1-甲基-3-丁烯基、2-甲基-3-丁烯基、3-甲基-3-丁烯基、1,1-二甲基-2-丙烯基、1,2-二甲基-1-丙烯基、1,2-二甲基-2-丙烯基、1-乙基-1-丙烯基、1-乙基-2-丙烯基、1-己烯基、2-己烯基、3-己烯基、4-己烯基、5-己烯基、1-甲基-1-戊烯基、2-甲基-1-戊烯基、3-甲基-1-戊烯基、4-甲基-1-戊烯基、1-甲基-2-戊烯基、2-甲基-2-戊烯基、3-甲基-2-戊烯基、4-甲基-2-戊烯基、1-甲基-3-戊烯基、2-甲基-3-戊烯基、3-甲基-3-戊烯基、4-甲基-3-戊烯基、1-甲基-4-戊烯基、2-甲基-4-戊烯基、3-甲基-4-戊烯基、4-甲基-4-戊烯基、1,1-二甲基-2-丁烯基、1,1-二甲基-3-丁烯基、1,2-二甲基-1-丁烯基、1,2-二甲基-2-丁烯基、1,2-二甲基-3-丁烯基、1,3-二甲基-1-丁烯基、1,3-二甲基-3-丁烯基、1,3-二甲基-3-丁烯基、2,2-二甲基-3-丁烯基、2,3-二甲基-1-丁烯基、2,3-二甲基-2-丁烯基、2,3-二甲基-3-丁烯基、3,3-二甲基-1-丁烯基、3,3-二甲基-2-丁烯基、1-乙基-1-丁烯基、1-乙基-2-丁烯基、1-乙基-3-丁烯基、2-乙基-1-丁烯基、2-乙基-2-丁烯基、2-乙基-3-丁烯基、1,1,2-三甲基-2-丙烯基、1-乙基-1-甲基-2-丙烯基、1-乙基-2-甲基-1-丙烯基和1-乙基-2-甲基-2-丙烯基;链烯氧基:经氧原子(-O-)与主结构相连的具有2到6个碳原子、双键可在任何位置的直链或支链链烯基;链烯硫基或链烯氨基:经硫原子(链烯硫基)或氮原子(链烯氨基)与主结构相连的、具有2以6个碳原子、双键可在任何位置的直链或支链链烯基;链烯羰基:经羰基(-CO-)与主结构相连的、具有2到10个碳原子、双键可在任何位置的直链或支链链烯基;链炔基:具有2到10个碳原子、叁键可在任何位置的直链或支链链炔基,例如C2-C6-链炔基,如乙炔基、2-丙炔基、2-丁炔基、3-丁炔基、1-甲基-2-丙炔基,2-戊炔基、3-戊炔基、4-戊炔基、1-甲基-2-丁炔基、1-甲基-3-丁炔基、2-甲基-3-丁炔基、1,1-二甲基-2-丙炔基、1-乙基-2-丙炔基、2-己炔基、3-己炔基、4-己炔基、5-己炔基、1-甲在-2-戊炔基、1-甲基-3-戊炔基、1-甲基-4-戊炔基、2-甲基-3-戊炔基、2-甲基-4-戊炔基、3-甲基-4-戊炔基、4-甲基-2-戊炔基、1,1-二甲基-2-丁炔基、1,1-二甲基-3-丁炔基、1,2-二甲基-3-丁炔基、2,2-二甲基-3-丁炔基、1-乙基-2-丁炔基、1-乙基-3-丁炔基、2-乙基-3-丁炔基和1-乙基-1-甲基-2-丙炔基;链炔氧基或链炔硫基和链炔氨基:经氧原子(链炔氧基)或硫原子(链炔硫基)或氮原子(链炔氨基)与主结构相连的、具有2到6个碳原子、叁键位于任何位置的直链或支链链炔基;链炔羰基:经羰基(-CO-)与主体结构相连的、具有3到10个碳原子、叁键位于任何位置的直链或支链链炔基;环烯基或环烯氧基、环烯硫基和环烯氨基:直接或经氧原子(环烯氧基)或硫原子(环烯硫基)或氮原子(环烯氨基)与主结构相连的、具有3到6个环碳原子的单环烯基,例如环丙烯基、环丁烯基、环戊烯基或环己烯基;环烷氧基或环烷硫基和环烷氨基:经氧原子(环烷氧基)或硫原子(环烷硫基)或氮原子(环烷氨基)与主结构相连、具有3到6个环碳原子的单环烷基,例如环丙基、环丁基、环戊基或环己基;杂环基或杂环氧基、杂环硫基和杂环氨基:直接或经氧原子(杂环氧基)或经硫原子(杂环硫基)或经氮原子(杂环氨基)与主结构相连的,含一到三个选自氧、氮和硫的杂原子的三到六元饱和或部分不饱和的单环或多环杂环,如2-四氢呋喃基,环氧乙烷基,3-四氢呋喃基,2-四氢噻吩基,3-四氢噻吩基,2-吡咯烷基,3-吡咯烷基,3-异噁唑烷基,4-异噁唑烷基,5-异噁唑烷基,3-异噻唑烷基,4-异噻唑烷基,5-异噻唑烷基,3-吡唑烷基,4-吡唑烷基,5-吡唑烷基,2-噁唑烷基,4-噁唑烷基,5-噁唑烷基,2-噻唑烷基,4-噻唑烷基,5-噻唑烷基,2-咪唑烷基,4-咪唑烷基,1,2,4-噁二唑烷-3-基,1,2,4-噁二唑烷-5-基,1,2,4-噻二唑烷-3-基,1,2,4-噻二唑烷-5-基,1,2,4-三唑烷-3-基,1,3,4-噁二唑烷-2-基,1,3,4-噻二唑烷-2-基,1,3,4-三唑烷-2-基,2,3-二氢呋喃-2-基,2,3-二氢呋喃-3-基,2,3-二氢呋喃-4-基,2,3-二氢呋喃-5-基,2,5-二氢呋喃-2-基,2,5-二氢呋喃-3-基,2,3-二氢噻吩-2-基,2,3-二氢噻吩-3-基,2,3-二氢噻吩-4-基,2,3-二氢噻吩-5-基,2,5-二氢噻吩-2-基,2,5-二氢噻吩-3-基,2,3-二氢吡咯-2-基,2,3-二氢吡咯-3-基,2,3-二氢吡咯-4-基,2,3-二氢吡咯-5-基,2,5-二氢吡咯-2-基,2,5-二氢吡咯-3-基,2,3-二氢异噁唑-3-基,2,3-二氢异噁唑-4-基,2,3-二氢异噁唑-5-基,4,5-二氢异噁唑-3-基,4,5-二氢异噁唑-4-基,4,5-二氢异噁唑-5-基,2,5-二氢异噻唑-3-基,2,5-二氢异噻唑-4-基,2,5-二氢异噻唑-5-基,2,3-二氢异吡唑-3-基,2,3-二氢异吡唑-4-基,2,3-二氢异吡唑-5-基,4,5-二氢异吡唑-3-基,4,5-二氢异吡唑-4-基,4,5-二氢异吡唑-5-基,2,5-二氢异吡唑-3-基,2,5-二氢异吡唑-4-基,2,5-二氢异吡唑-5-基,2,3-二氢噁唑-3-基,2,3-二氢噁唑-4-基,2,3-二氢噁唑-5-基,4,5-二氢噁唑-3-基,4,5-二氢噁唑-4-基,4,5-二氢噁唑-5-基,2,5-二氢噁唑-3-基,2,5-二氢噁唑-4-基,2,5-二氢噁唑-5-基,2,3-二氢噻唑-2-基,2,3-二氢噻唑-4-基,2,3-二氢噻唑-5-基,4,5-二氢噻唑-2-基,4,5-二氢噻唑-4-基,4,5-二氢噻唑-5-基,2,5-二氢噻唑-2-基,2,5-二氢噻唑-4-基,2,5-二氢噻唑-5-基,2,3-二氢咪唑-2-基,2,3-二氢咪唑-4-基,2,3-二氢咪唑-5-基,4,5-二氢咪唑-2-基,4,5-二氢咪唑-4-基,4,5-二氢咪唑-5-基,2,5-二氢咪唑-2-基,2,5-二氢咪唑-4-基,2,5-二氢咪唑-5-基,2-吗啉基,3-吗啉基,2-哌啶基,3-哌啶基,4-哌啶基,3-四氢哒嗪基,4-四氢哒嗪基,2-四氢嘧啶基,4-四氢嘧啶基,5-四氢嘧啶基,2-四氢吡嗪基,1,3,5-四氢三嗪-2-基,1,2,4-四氢三嗪-3-基,1,3-二氢噁嗪-2-基,1,3-二噻烷-2-基,2-四氢吡喃基,1,3-二噁烷-2-基,2,4,5,6-四氢吡啶-2-基,4H-1,3-噻嗪-2-基,4H-3,1-苯并噻嗪-2-基,1,1-二氧代-2,3,4,5-四氢噻吩-2-基,2H-1,4-苯并噻嗪-3-基,2H-1,4-苯并噁嗪-3-基,1,3-二氢噁嗪-2-基,1,3-二噻烷-2-基;芳基或芳氧基、芳硫基、芳羰基和芳磺酰基:直接或经氧原子(-O-)(芳氧基)或硫原子(-S-)(芳硫基)、经羰基(-CO-)(芳羰基)或磺酰基(-SO2-)(芳磺酰基)与主结构相连的芳香单环或多环烃基,例如苯基、萘基和菲基或苯氧基、萘氧基和菲氧基以及相应的羰基和磺酰基;芳氨基:经氮原子与主结构相连的芳香单环或多环烃基;杂芳基或杂芳氧基、杂芳硫基、杂芳羰基和杂芳磺酰基:直接或经氧原子(-O-)(杂芳氧基)或硫原子(-S-)(杂芳硫基)、经羰基(-CO-)(杂芳羰基)或磺酰基(-SO2-)(杂芳磺酰基)与主结构相连的,除碳原子外可含一到四个氮原子、或一到三个氮原子和氧或硫原子、或含一个氧原子或一个硫原子的芳香单环或多环基团,例如,-
含一到三个氮原子的5元杂芳基:除碳原子外可含一到三个环氮原子
的5-元环杂芳基,例如2-吡咯基,3-吡咯基,3-吡唑基,4
-吡唑基,5-吡唑基,2-咪唑基,4-咪唑基,1,2,4-三
唑-3-基和1,3,4-三唑-2-基;-
含一到四个氮原子,或一到三个氮原子和一个硫或氧原子,或含一个
硫或一个氧原子的5-元杂芳基:除碳原子外,可含一到四个氮原子、
或一到三个氮原子和一个硫或氧原子、或含一个硫或一个氧原子的环
原子的5元环杂芳基,例如2-呋喃基,3-呋喃基,2-噻吩基,3
-噻吩基,2-吡咯基,3-吡咯基,3-异噁唑基,4-异噁唑基,
5-异噁唑基,3-异噻唑基,4-异噻唑基,5-异噻唑基,3-吡
唑基,4-吡唑基,5-吡唑基,2-噁唑基,4-噁唑基,5-噁
唑基,2-噻唑基,4-噻唑基,5-噻唑基,2-咪唑基,4-咪
唑基,1,2,4-噁二唑-3-基,1,2,4-噁二唑-5-基,
1,2,4-噻二唑-3-基,1,2,4-噻二唑-5-基,1,2,
4-三唑-3-基,1,3,4-噁二唑-2-基,1,3,4-噻二
唑-2-基,1,3,4-三唑-2-基;-
含一到三个氮原子或含一个氮原子和/或一个氧或硫原子的与苯稠合的
5-元杂芳基:除碳原子外,可含有一到四个氮原子,或一到三个氮原
子和一个硫或氧原子,或一个氧或一个硫原子的环原子的5元环杂芳
基,其中两个相邻环碳原子,或一个环氮原子与相邻的环碳原子可被
丁-1,3-二烯-1,4-二基桥连。-
经氮原子连接的含一到四个氮原子的5元杂芳基,或经氮原子连接的
含一到三个氮原子的与苯环稠合的5元杂芳基:除碳原子外,可含有
一到四个氮原子,或一到三个氮原子的环原子的5元环杂芳基,其中
两个相邻的环碳原子或一个环氮原子与相邻的环碳原子可被丁-1,
3-二烯-1,4-二基桥连,这些基团经一个环氮原子与主结构相
连;-
含一到三个或一到四个氮原子的6元杂芳基:除碳原子外,可含有一
到三个或一到四个环氮原子的6元环杂芳基,例如2-吡啶基,3-
吡啶基,4-吡啶基,3-哒嗪基,4-哒嗪基,2-嘧啶基,4-
嘧啶基,5-嘧啶基,2-吡嗪基,1,3,5-三嗪-2-基,1,
2,4-三嗪-3-基和1,2,4,5-四嗪-3-基;-
含一到四个氮原子的与苯环稠合的6元杂芳基:两个相邻的环碳原子
可被丁-1,3-二烯-1,4-二基桥连的6元环杂芳基,例如喹
啉,异喹啉,喹唑啉和喹喔啉;或相应的氧基、硫基、羰基或磺酰基;杂芳氨基:经氮原子与主结构相连的,除环碳原子外可另外含有一到四个氮原子或一到三氮原子和一个氧或一个硫原子的芳香单环或多环基。
“部分或完全卤化”指在被定义的基团中的氢原子部分地或完全地被相同或不同的上述卤原子取代。
考虑到其生物活性,优选其中m为0的式I化合物。
同样也优选其中R1为甲基的式I化合物。
另外,优选其中R3为氢、羟基、环丙基、氯、甲基、乙基、1-甲基乙基、甲氧基、甲硫基或苯基的化合物I。
另外,优选其中R3为甲基的化合物I。
另外,优选其中R3为甲氧基的化合物I。
另外,优选其中R3为羟基的化合物I。
另外,优选其中R3为氯的化合物I。
另外,优选其中R4为氢、羟基、环丙基、氯、甲基、乙基、异丙基、甲氧基和甲硫基的化合物I。
另外,优选其中R4为甲基的化合物I。
另外,优选其中R4为甲氧基的化合物I。
另外,优选其中R4为羟基的化合物I。
另外,优选其中R4为乙基的化合物I。
另外,优选其中R4为异丙基的化合物I。
另外,优选其中R4为环丙基的化合物I。
另外,优选其中R4为未取代或取代的芳基或杂芳基的化合物I。
另外,优选其中R4为未取代或取代的吡啶基、嘧啶基、吡嗪基、哒嗪基或三嗪基的化合物I。
另外,优选其中R4为未取代或取代的呋喃基,噻吩基或吡咯基的化合物I。
另外,优选其中R4为未取代或取代的噁唑基、噻唑基、异噁唑基、异噻唑基、吡唑基或咪唑基的化合物I。
另外,优选其中R4为未取代或取代的噁二唑基、噻二唑基或三唑基的化合物I。
另外,优选其中R4为未取代或由选自硝基、氰基、羟基、氨基、氨羰基、氨基硫代羰基、卤素、C1-C4-烷基、C1-C4卤代烷基、C1-C4-烷氧基、C1-C4-卤代烷氧基、C1-C4-烷氨基、双-C1-C4-烷基氨基、C1-C4-烷基磺酰基、C1-C4-烷氧羰基、C1-C4-烷氨基羰基或双-C1-C4-烷基氨基羰基的1或2个基团取代的苯基的化合物I。
另外,优选其中R5为氢、C1-C6-烷基、芳烷基、杂芳烷基、芳氧烷基、杂芳氧烷基、芳基或杂芳基的化合物I。
另外,优选其中R5为C1-C6-烷基的化合物I。
另外,优选其中R5为甲基或乙基的化合物I。
另外,优选其中R5为芳烷基或杂芳烷基的化合物I。
另外,优选其中R5为芳氧烷基或杂芳氧烷基的化合物I。
另外,优选其中R5为芳基或杂芳基的化合物I。
另外,优选其中X为NOCH3的化合物I。
另外,优选其中X为CHOCH3的化合物I。
另外,优选其中X为CHCH3或CHCH2CH3的化合物I。
考虑到其用途,特别优选下列表中所收编的化合物I。表1
通式I.1的化合物,其中(R2)m为氯,每一个化合物中取代基R3、R4和R5的组合与表A中的一行对应。表3
通式I.2的化合物,其中(R2)m为氯,每一个化合物中的取代基R3、R4和R5的组合与表A中的一行对应。表5
通式I.3的化合物,其中(R2)m为氢,每一个化合物中的取代基R3、R4和R5的组合与表A中的一行对应。表6
通式I.3的化合物,其中(R2)m为氯,每一个化合物中的取代基R3、R4和R5的组合与表A中的一行对应。表7
通式I.4的化合物,其中(R2)m为氯,每一个化合物中的取代基R3、R4和R5的组合与表A中的一行对应。 表A
No. | R3 | R4 | R5 |
1 | CH3 | CH3 | H |
2 | CH3 | CH3 | CH3 |
3 | CH3 | CH3 | C2H5 |
4 | CH3 | CH3 | n-C3H7 |
5 | CH3 | CH3 | i-C3H7 |
6 | CH3 | CH3 | 环丙基 |
7 | CH3 | CH3 | n-C4H9 |
8 | CH3 | CH3 | s-C4H9 |
9 | CH3 | CH3 | i-C4H9 |
10 | CH3 | CH3 | t-C4H9 |
11 | CH3 | CH3 | n-C5H11 |
12 | CH3 | CH3 | i-C5H11 |
13 | CH3 | CH3 | neo-C5H11 |
14 | CH3 | CH3 | 环戊基 |
15 | CH3 | CH3 | n-C6H13 |
16 | CH3 | CH3 | 环已基 |
17 | CH3 | CH3 | n-C8H17 |
18 | CH3 | CH3 | CH2CH2Cl |
No. | R3 | R4 | R5 |
19 | CH3 | CH3 | (CH2)4Cl |
20 | CH3 | CH3 | CH2CN |
21 | CH3 | CH3 | CH2CH2CN |
22 | CH3 | CH3 | (CH2)3CN |
23 | CH3 | CH3 | (CH2)4CN |
24 | CH3 | CH3 | (CH2)6CN |
25 | CH3 | CH3 | 环己基甲基 |
26 | CH3 | CH3 | 2-环己基乙-1-基 |
27 | CH3 | CH3 | 环丙基甲基 |
28 | CH3 | CH3 | 2-环丙基乙-1-基 |
29 | CH3 | CH3 | 2-甲氧基乙-1-基 |
30 | CH3 | CH3 | 2-乙氧基乙-1-基 |
31 | CH3 | CH3 | 2-异丙氧基乙-1-基 |
32 | CH3 | CH3 | 3-甲氧基丙-1-基 |
33 | CH3 | CH3 | 3-乙氧基丙-1-基 |
34 | CH3 | CH3 | 3-异丙氧基丙-1-基 |
35 | CH3 | CH3 | 4-甲氧基丁-1-基 |
36 | CH3 | CH3 | 4-异丙氧基丁-1-基 |
37 | CH3 | CH3 | 丙烯-3-基 |
38 | CH3 | CH3 | 丁-2-烯-1-基 |
No. | R3 | R4 | R5 |
39 | CH3 | CH3 | 3-甲基丁-2-烯-1-基 |
40 | CH3 | CH3 | 2-乙烯氧基乙-1-基 |
41 | CH3 | CH3 | 烯丙氧基乙-1-基 |
42 | CH3 | CH3 | 2-三氟甲氧基乙-1-基 |
43 | CH3 | CH3 | 3-三氟甲氧基丙-1-基 |
44 | CH3 | CH3 | 4-二氟甲氧基丁-1-基 |
45 | CH3 | CH3 | 羟基羰基甲基 |
46 | CH3 | CH3 | 甲氧羰基甲基 |
47 | CH3 | CH3 | 氨羰基甲基 |
48 | CH3 | CH3 | N-甲基氨羰基甲基 |
49 | CH3 | CH3 | N,N-二甲基氨基羰基甲基 |
50 | CH3 | CH3 | 2-羟基羰基乙-1-基 |
51 | CH3 | CH3 | 2-甲氧羰基乙-1-基 |
52 | CH3 | CH3 | 2-氨羰基乙-1-基 |
53 | CH3 | CH3 | 2-N-甲基氨羰基乙-1-基 |
54 | CH3 | CH3 | 2-二甲氨基羰基乙-1-基 |
55 | CH3 | CH3 | 2-氨基乙-1-基 |
56 | CH3 | CH3 | 2-氨基丙-1-基 |
57 | CH3 | CH3 | 4-氨基丁-1-基 |
58 | CH3 | CH3 | 3-二甲氨基丙-1-基 |
No. | R3 | R4 | R5 |
59 | CH3 | CH3 | 4-氨基硫代羰基丁-1-基 |
60 | CH3 | CH3 | 2-氧代丙基 |
61 | CH3 | CH3 | 环己基 |
62 | CH3 | CH3 | 环丙基 |
63 | CH3 | CH3 | 环戊基 |
64 | CH3 | CH3 | 2-甲氧亚氨基丙-1-基 |
65 | CH3 | CH3 | 2-甲氧亚氨基乙-1-基 |
66 | CH3 | CH3 | 6-氨羰基己-1-基 |
67 | CH3 | CH3 | 3-氨基硫代羰基丙-1-基 |
68 | CH3 | CH3 | 2-氨基硫代羰基乙-1-基 |
69 | CH3 | CH3 | 氨基硫代羰基甲基 |
70 | CH3 | CH3 | 4-(N,N-二甲氨基)丁-1-基 |
71 | CH3 | CH3 | 2-(甲硫基)乙-1-基 |
72 | CH3 | CH3 | 2-(甲磺酰基)乙-1-基 |
73 | CH3 | CH3 | 4-(甲硫基)丙-1-基 |
74 | CH3 | CH3 | 4-(甲磺酰基)丙-1-基 |
75 | CH3 | CH3 | 苄基 |
76 | CH3 | CH3 | 2-F-C6H4-CH2 |
77 | CH3 | CH3 | 3-F-C6H4-CH2 |
78 | CH3 | CH3 | 4-F-C6H4-CH2 |
No. | R3 | R4 | R5 |
79 | CH3 | CH3 | 2,3-F2-C6H3-CH2 |
80 | CH3 | CH3 | 2,4-F2-C6H3-CH2 |
81 | CH3 | CH3 | 2,5-F2-C6H3-CH2 |
82 | CH3 | CH3 | 2,6-F2-C6H3-CH2 |
83 | CH3 | CH3 | 3,4-F2-C6H3-CH2 |
84 | CH3 | CH3 | 3,5-F2-C6H3-CH2 |
85 | CH3 | CH3 | 2-Cl-C6H4-CH2 |
86 | CH3 | CH3 | 3-Cl-C6H4-CH2 |
87 | CH3 | CH3 | 4-Cl-C6H4-CH2 |
88 | CH3 | CH3 | 2,3-Cl2-C6H3-CH2 |
89 | CH3 | CH3 | 2,4-Cl2-C6H3-CH2 |
90 | CH3 | CH3 | 2,5-Cl2-C6H3-CH2 |
91 | CH3 | CH3 | 2,6-Cl2-C6H3-CH2 |
92 | CH3 | CH3 | 3,4-Cl2-C6H3-CH2 |
93 | CH3 | CH3 | 3,5-Cl2-C6H3-CH2 |
94 | CH3 | CH3 | 2,3,4-Cl3-C6H2-CH2 |
95 | CH3 | CH3 | 2,3,5-Cl3-C6H2-CH2 |
96 | CH3 | CH3 | 2,3,6-Cl3-C6H2-CH2 |
97 | CH3 | CH3 | 2,4,5-Cl3-C6H2-CH2 |
98 | CH3 | CH3 | 2,4,6-Cl3-C6H2-CH2 |
No. | R3 | R4 | R5 |
99 | CH3 | CH3 | 3,4,5-Cl3-C6H2-CH2 |
100 | CH3 | CH3 | 2-Br-C6H4-CH2 |
101 | CH3 | CH3 | 3-Br-C6H4-CH2 |
102 | CH3 | CH3 | 4-Br-C6H4-CH2 |
103 | CH3 | CH3 | 2,3-Br2-C6H3-CH2 |
104 | CH3 | CH3 | 2,4-Br2-C6H3-CH2 |
105 | CH3 | CH3 | 2,5-Br2-C6H3-CH2 |
106 | CH3 | CH3 | 2,6-Br2-C6H3-CH2 |
107 | CH3 | CH3 | 3,4-Br2-C6H3-CH2 |
108 | CH3 | CH3 | 3,5-Br2-C6H3-CH2 |
109 | CH3 | CH3 | 2-F,3-Cl-C6H3-CH2 |
110 | CH3 | CH3 | 2-F,4-Cl-C6H3-CH2 |
111 | CH3 | CH3 | 2-F,5-Cl-C6H3-CH2 |
112 | CH3 | CH3 | 2-F,3-Br-C6H3-CH2 |
113 | CH3 | CH3 | 2-F,4-Br-C6H3-CH2 |
114 | CH3 | CH3 | 2-F,5-Br-C6H3-CH2 |
115 | CH3 | CH3 | 2-Cl,3-Br-C6H3-CH2 |
116 | CH3 | CH3 | 2-Cl,4-Br-C6H3-CH2 |
117 | CH3 | CH3 | 2-Cl,5-Br-C6H3-CH2 |
118 | CH3 | CH3 | 3-F,4-Cl-C6H3-CH2 |
No. | R3 | R4 | R5 |
119 | CH3 | CH3 | 3-F,5-Cl-C6H3-CH2 |
120 | CH3 | CH3 | 3-F,6-Cl-C6H3-CH2 |
121 | CH3 | CH3 | 3-F,4-Br-C6H3-CH2 |
122 | CH3 | CH3 | 3-F,5-Br-C6H3-CH2 |
123 | CH3 | CH3 | 3-F,6-Br-C6H3-CH2 |
124 | CH3 | CH3 | 3-Cl,4-Br-C6H3-CH2 |
125 | CH3 | CH3 | 3-Cl,5-Br-C6H3-CH2 |
126 | CH3 | CH3 | 3-Cl,6-Br-C6H3-CH2 |
127 | CH3 | CH3 | 4-F,5-Cl-C6H3-CH2 |
128 | CH3 | CH3 | 4-F,6-Cl-C6H3-CH2 |
129 | CH3 | CH3 | 4-F,5-Br-C6H3-CH2 |
130 | CH3 | CH3 | 4-F,6-Br-C6H3-CH2 |
131 | CH3 | CH3 | 4-Cl,5-Br-C6H3-CH2 |
132 | CH3 | CH3 | 5-F,6-Cl-C6H3-CH2 |
133 | CH3 | CH3 | 5-F,6-Br-C6H3-CH2 |
134 | CH3 | CH3 | 5-Cl,6-Br-C6H3-CH2 |
135 | CH3 | CH3 | 3-Br,4-Cl,5-Br-C6H2-CH2 |
136 | CH3 | CH3 | 2-CN-C6H4-CH2 |
137 | CH3 | CH3 | 3-CN-C6H4-CH2 |
138 | CH3 | CH3 | 4-CN-C6H4-CH2 |
No. | R3 | R4 | R5 |
139 | CH3 | CH3 | 2-NO2-C6H4-CH2 |
140 | CH3 | CH3 | 3-NO2-C6H4-CH2 |
141 | CH3 | CH3 | 4-NO2-C6H4-CH2 |
142 | CH3 | CH3 | 2-CH3-C6H4-CH2 |
143 | CH3 | CH3 | 3-CH3-C6H4-CH2 |
144 | CH3 | CH3 | 4-CH3-C6H4-CH2 |
145 | CH3 | CH3 | 2,3-(CH3)2-C6H3-CH2 |
146 | CH3 | CH3 | 2,4-(CH3)2-C6H3-CH2 |
147 | CH3 | CH3 | 2,5-(CH3)2-C6H3-CH2 |
148 | CH3 | CH3 | 2,6-(CH3)2-C6H3-CH2 |
149 | CH3 | CH3 | 3,4-(CH3)2-C6H3-CH2 |
150 | CH3 | CH3 | 3,5-(CH3)2-C6H3-CH2 |
151 | CH3 | CH3 | 2-C2H5-C6H4-CH2 |
152 | CH3 | CH3 | 3-C2H5-C6H4-CH2 |
153 | CH3 | CH3 | 4-C2H5-C6H4-CH2 |
154 | CH3 | CH3 | 2-i-C3H7-C6H4-CH2 |
155 | CH3 | CH3 | 3-i-C3H7-C6H4-CH2 |
156 | CH3 | CH3 | 4-i-C3H7-C6H4-CH2 |
157 | CH3 | CH3 | 2-环己基-C6H4-CH2 |
158 | CH3 | CH3 | 3-环己基-C6H4-CH2 |
No. | R3 | R4 | R5 |
159 | CH3 | CH3 | 4-环己基-C6H4-CH2 |
160 | CH3 | CH3 | 2-乙烯基-C6H4-CH2 |
161 | CH3 | CH3 | 3-乙烯基-C6H4-CH2 |
162 | CH3 | CH3 | 4-乙烯基-C6H4-CH2 |
163 | CH3 | CH3 | 2-烯丙基-C6H4-CH2 |
164 | CH3 | CH3 | 3-烯丙基-C6H4-CH2 |
165 | CH3 | CH3 | 4-烯丙基-C6H4-CH2 |
166 | CH3 | CH3 | 2-C6H5-C6H4-CH2 |
167 | CH3 | CH3 | 3-C6H5-C6H4-CH2 |
168 | CH3 | CH3 | 4-C6H5-C6H4-CH2 |
169 | CH3 | CH3 | 3-CH3,5-t-C4H9-C6H3-CH2 |
170 | CH3 | CH3 | 2-OH-C6H4-CH2 |
171 | CH3 | CH3 | 3-OH-C6H4-CH2 |
172 | CH3 | CH3 | 4-OH-C6H4-CH2 |
173 | CH3 | CH3 | 2-OCH3-C6H4-CH2 |
174 | CH3 | CH3 | 3-OCH3-C6H4-CH2 |
175 | CH3 | CH3 | 4-OCH3-C6H4-CH2 |
176 | CH3 | CH3 | 2,3-(OCH3)2-C6H3-CH2 |
177 | CH3 | CH3 | 2,4-(OCH3)2-C6H3-CH2 |
178 | CH3 | CH3 | 2,5-(OCH3)2-C6H3-CH2 |
No. | R3 | R4 | R5 |
179 | CH3 | CH3 | 3,4-(OCH3)2-C6H3-CH2 |
180 | CH3 | CH3 | 3,5-(OCH3)2-C6H3-CH2 |
181 | CH3 | CH3 | 3,4,5-(OCH3)3-C6H2-CH2 |
182 | CH3 | CH3 | 2-OC2H5-C6H4-CH2 |
183 | CH3 | CH3 | 3-OC2H5-C6H4-CH2 |
184 | CH3 | CH3 | 4-OC2H5-C6H4-CH2 |
185 | CH3 | CH3 | 2-O-(n-C3H7)-C6H4-CH2 |
186 | CH3 | CH3 | 3-O-(n-C3H7)-C6H4-CH2 |
187 | CH3 | CH3 | 4-O-(n-C3H7)-C6H4-CH2 |
188 | CH3 | CH3 | 2-O-(i-C3H7)-C6H4-CH2 |
189 | CH3 | CH3 | 3-O-(i-C3H7)-C6H4-CH2 |
190 | CH3 | CH3 | 4-O-(i-C3H7)-C6H4-CH2 |
191 | CH3 | CH3 | 4-O-(n-C4H9)-C6H4-CH2 |
192 | CH3 | CH3 | 3-O-(t-C4H9)-C6H4-CH2 |
193 | CH3 | CH3 | 4-O-(n-C6H13)-C6H4-CH2 |
194 | CH3 | CH3 | 2-O-烯丙基-C6H4-CH2 |
195 | CH3 | CH3 | 3-O-烯丙基-C6H4-CH2 |
196 | CH3 | CH3 | 4-O-烯丙基-C6H4-CH2 |
197 | CH3 | CH3 | 2-CF3-C6H4-CH2 |
198 | CH3 | CH3 | 3-CF3-C6H4-CH2 |
No. | R3 | R4 | R5 |
199 | CH3 | CH3 | 4-CF3-C6H4-CH2 |
200 | CH3 | CH3 | 2-乙酰基-C6H4-CH2 |
201 | CH3 | CH3 | 3-乙酰基-C6H4-CH2 |
202 | CH3 | CH3 | 4-乙酰基-C6H4-CH2 |
203 | CH3 | CH3 | 2-甲氧羰基-C6H4-CH2 |
204 | CH3 | CH3 | 3-甲氧羰基-C6H4-CH2 |
205 | CH3 | CH3 | 4-甲氧羰基-C6H4-CH2 |
206 | CH3 | CH3 | 2-氨羰基-C6H4-CH2 |
207 | CH3 | CH3 | 3-氨羰基-C6H4-CH2 |
208 | CH3 | CH3 | 4-氨羰基-C6H4-CH2 |
209 | CH3 | CH3 | 2-二甲氨基羰基-C6H4-CH2 |
210 | CH3 | CH3 | 3-二甲氨基羰基-C6H4-CH2 |
211 | CH3 | CH3 | 4-二甲氨基羰基-C6H4-CH2 |
212 | CH3 | CH3 | 2-(N-甲氨基羰基)-C6H4-CH2 |
213 | CH3 | CH3 | 3-(N-甲氨基羰基)-C6H4-CH2 |
214 | CH3 | CH3 | 4-(N-甲氨基羰基)-C6H4-CH2 |
215 | CH3 | CH3 | 2-H2N-C6H4-CH2 |
216 | CH3 | CH3 | 3-H2N-C6H4-CH2 |
217 | CH3 | CH3 | 4-H2N-C6H4-CH2 |
218 | CH3 | CH3 | 2-氨基硫代羰基-C6H4-CH2 |
No. | R3 | R4 | R5 |
219 | CH3 | CH3 | 3-氨基硫代羰基-C6H4-CH2 |
220 | CH3 | CH3 | 4-氨基硫代羰基-C6H4-CH2 |
221 | CH3 | CH3 | 2-甲氧基亚氨基甲基-C6H4-CH2 |
222 | CH3 | CH3 | 3-甲氧基亚氨基甲基-C6H4-CH2 |
223 | CH3 | CH3 | 4-甲氧基亚氨基甲基-C6H4-CH2 |
224 | CH3 | CH3 | 2-甲酰基-C6H4-CH2 |
225 | CH3 | CH3 | 3-甲酰基-C6H4-CH2 |
226 | CH3 | CH3 | 4-甲酰基-C6H4-CH2 |
227 | CH3 | CH3 | 2-(1′-甲氧基亚氨基乙-1’-基)-C6H4-CH2 |
228 | CH3 | CH3 | 3-(1′-甲氧基亚氨基乙-1’-基)-C6H4-CH2 |
229 | CH3 | CH3 | 4-(1′-甲氧基亚氨基乙-1’-基)-C6H4-CH2 |
230 | CH3 | CH3 | 2-SCH3-C6H4-CH2 |
231 | CH3 | CH3 | 3-SCH3-C6H4-CH2 |
232 | CH3 | CH3 | 4-SCH3-C6H4-CH2 |
233 | CH3 | CH3 | 2-SO2CH3-C6H4-CH2 |
234 | CH3 | CH3 | 3-SO2CH3-C6H4-CH2 |
235 | CH3 | CH3 | 4-SO2CH3-C6H4-CH2 |
236 | CH3 | CH3 | 2-OCF3-C6H4-CH2 |
237 | CH3 | CH3 | 3-OCF3-C6H4-CH2 |
238 | CH3 | CH3 | 4-OCF3-C6H4-CH2 |
No. | R3 | R4 | R5 |
239 | CH3 | CH3 | 2-OCHF2-C6H4-CH2 |
240 | CH3 | CH3 | 3-OCHF2-C6H4-CH2 |
241 | CH3 | CH3 | 4-OCHF2-C6H4-CH2 |
242 | CH3 | CH3 | 3-CF3,4-OCF3-C6H3-CH2 |
243 | CH3 | CH3 | 1-荼基-CH2 |
244 | CH3 | CH3 | 2-荼基-CH2 |
245 | CH3 | CH3 | 2-苯氧乙-1-基 |
246 | CH3 | CH3 | 2-(2′-氯苯氧基)乙-1-基 |
247 | CH3 | CH3 | 2-(3′-氯苯氧基)乙-1-基 |
248 | CH3 | CH3 | 2-(4′-氯苯氧基)乙-1-基 |
249 | CH3 | CH3 | 2-(3′,5′-二氯苯氧基)乙-1-基 |
250 | CH3 | CH3 | 2-(2′-氰基苯氧基)乙-1-基 |
251 | CH3 | CH3 | 2-(3′-氰基苯氧基)乙-1-基 |
252 | CH3 | CH3 | 2-(4′-氰基苯氧基)乙-1-基 |
253 | CH3 | CH3 | 2-(2′-甲基苯氧基)乙-1-基 |
254 | CH3 | CH3 | 2-(3′-甲基苯氧基)乙-1-基 |
255 | CH3 | CH3 | 2-(4′-甲基苯氧基)乙-1-基 |
256 | CH3 | CH3 | 2-(3′-叔丁基苯氧基)乙-1-基 |
257 | CH3 | CH3 | 2-(4′-叔丁基苯氧基)乙-1-基 |
258 | CH3 | CH3 | 2-(2′硝基苯氧基)乙-1-基 |
No. | R3 | R4 | R5 |
259 | CH3 | CH3 | 2-(3′-硝基苯氧基)乙-1-基 |
260 | CH3 | CH3 | 2-(4′-硝基苯氧基)乙-1-基 |
261 | CH3 | CH3 | 2-(2′-甲氧苯氧基)乙-1-基 |
262 | CH3 | CH3 | 2-(3′-甲氧苯氧基)乙-1-基 |
263 | CH3 | CH3 | 2-(4′-甲氧苯氧基)乙-1-基 |
264 | CH3 | CH3 | 2-(2′-三氟甲基苯氧基)乙-1-基 |
265 | CH3 | CH3 | 2-(3′-三氟甲基苯氧基)乙-1-基 |
266 | CH3 | CH3 | 2-(4′-三氟甲基苯氧基)乙-1-基 |
267 | CH3 | CH3 | 2-(2′-乙酰基苯氧基)乙-1-基 |
268 | CH3 | CH3 | 2-(3′-乙酰基苯氧基)乙-1-基 |
269 | CH3 | CH3 | 2-(4′-乙酰基苯氧基)乙-1-基 |
270 | CH3 | CH3 | 2-(2′-甲氧羰基)乙-1-基 |
271 | CH3 | CH3 | 2-(3′-甲氧羰基)乙-1-基 |
272 | CH3 | CH3 | 2-(4′-甲氧羰基)乙-1-基 |
273 | CH3 | CH3 | 2-(2′-二甲氨基羰基)乙-1-基 |
274 | CH3 | CH3 | 2-(3′-二甲氨基羰基)乙-1-基 |
275 | CH3 | CH3 | 2-(4′-二甲氨基羰基)乙-1-基 |
276 | CH3 | CH3 | 2-(2′-氨基硫代羰基)乙-1-基 |
277 | CH3 | CH3 | 2-(3′-氨基硫代羰基)乙-1-基 |
278 | CH3 | CH3 | 2-(4′-氨基硫代羰基)乙-1-基 |
No. | R3 | R4 | R5 |
279 | CH3 | CH3 | 2-(2′-甲磺酰基)乙-1-基 |
280 | CH3 | CH3 | 2-(3′-甲磺酰基)乙-1-基 |
281 | CH3 | CH3 | 2-(4′-甲磺酰基)乙-1-基 |
282 | CH3 | CH3 | 3-苯氧基丙-1-基 |
283 | CH3 | CH3 | 3-(2′-氯苯氧基)丙-1-基 |
284 | CH3 | CH3 | 3-(3′-氯苯氧基)丙-1-基 |
285 | CH3 | CH3 | 3-(4′-氯苯氧基)丙-1-基 |
286 | CH3 | CH3 | 3-(3’,5’,二氯苯氧基)丙-1-基 |
287 | CH3 | CH3 | 3-(2′-氰基苯氧基)丙-1-基 |
288 | CH3 | CH3 | 3-(3′-氰基苯氧基)丙-1-基 |
289 | CH3 | CH3 | 3-(4′-氰基苯氧基)丙-1-基 |
290 | CH3 | CH3 | 3-(2′-甲基苯氧基)丙-1-基 |
291 | CH3 | CH3 | 3-(3′-甲基苯氧基)丙-1-基 |
292 | CH3 | CH3 | 3-(4′-甲基苯氧基)丙-1-基 |
293 | CH3 | CH3 | 3-(2′-甲氧基苯氧基)丙-1-基 |
294 | CH3 | CH3 | 3-(3′甲氧基苯氧基)丙-1-基 |
295 | CH3 | CH3 | 3-(4′-甲氧基苯氧基)丙-1-基 |
296 | CH3 | CH3 | 3-(2′-三氟甲基苯氧基)丙-1-基 |
297 | CH3 | CH3 | 3-(3′-三氟甲基苯氧基)丙-1-基 |
298 | CH3 | CH3 | 3-(4′-三氟甲基苯氧基)丙-1-基 |
No. | R3 | R4 | R5 |
299 | CH3 | CH3 | 4-苯氧基丁-1-基 |
300 | CH3 | CH3 | 2-苯基乙-1-基 |
301 | CH3 | CH3 | 2-(2′-氯苯基)乙-1-基 |
302 | CH3 | CH3 | 2-(3′-氯苯基)乙-1-基 |
303 | CH3 | CH3 | 2-(4′-氯苯基)乙-1-基 |
304 | CH3 | CH3 | 2-(3′,5′-二氯苯基)乙-1-基 |
305 | CH3 | CH3 | 2-(2′-氰基苯基)乙-1-基 |
306 | CH3 | CH3 | 2-(3′-氰基苯基)乙-1-基 |
307 | CH3 | CH3 | 2-(4′-氰基苯基)乙-1-基 |
308 | CH3 | CH3 | 2-(2′-甲基苯基)乙-1-基 |
309 | CH3 | CH3 | 2-(3′-甲基苯基)乙-1-基 |
310 | CH3 | CH3 | 2-(4′-甲基苯基)乙-1-基 |
311 | CH3 | CH3 | 2-(2′-甲氧苯基)乙-1-基 |
312 | CH3 | CH3 | 2-(3′-甲氧苯基)乙-1-基 |
313 | CH3 | CH3 | 2-(4′-甲氧苯基)乙-1-基 |
314 | CH3 | CH3 | 2-(2′-三氟甲基苯基)乙-1-基 |
315 | CH3 | CH3 | 2-(3′-三氟甲基苯基)乙-1-基 |
316 | CH3 | CH3 | 2-(4′-三氟甲基苯基)乙-1-基 |
317 | CH3 | CH3 | 3-苯基丙-1-基 |
318 | CH3 | CH3 | 3-(2’-氯苯基)丙-1-基 |
No. | R3 | R4 | R5 |
319 | CH3 | CH3 | 3-(3′-氯苯基)丙-1-基 |
320 | CH3 | CH3 | 3-(4′-氯苯基)丙-1-基 |
321 | CH3 | CH3 | 3-(2′-氰基苯基)丙-1-基 |
322 | CH3 | CH3 | 3-(3′-氰基苯基)丙-1-基 |
323 | CH3 | CH3 | 3-(4′-氰基苯基)丙-1-基 |
324 | CH3 | CH3 | 3-(2’-三氟甲基苯基)丙-1-基 |
325 | CH3 | CH3 | 4-苯基丁-1-基 |
326 | CH3 | CH3 | 4-(4’-氯苯基)丁-1-基 |
327 | CH3 | CH3 | 6-(4’-氯苯基)己-1-基 |
328 | CH3 | CH3 | 2-吡啶甲基 |
329 | CH3 | CH3 | 3-吡啶甲基 |
330 | CH3 | CH3 | 4-吡啶甲基 |
331 | CH3 | CH3 | 4-氯吡啶-2-基甲基 |
332 | CH3 | CH3 | 5-氯吡啶-2-基甲基 |
333 | CH3 | CH3 | 6-氯吡啶-2-基甲基 |
334 | CH3 | CH3 | 5-氯吡啶-3-基甲基 |
335 | CH3 | CH3 | 6-氯吡啶-3-基甲基 |
336 | CH3 | CH3 | 2-氯吡啶-4-基甲基 |
337 | CH3 | CH3 | 2-嘧啶甲基 |
338 | CH3 | CH3 | 4-氯嘧啶-2-基甲基 |
No. | R3 | R4 | R5 |
339 | CH3 | CH3 | 5-氯嘧啶-2-基甲基 |
340 | CH3 | CH3 | 2-氯嘧啶-4-基甲基 |
341 | CH3 | CH3 | 6-氯嘧啶-4-基甲基 |
342 | CH3 | CH3 | 2-氯嘧啶-5-基甲基 |
343 | CH3 | CH3 | 4-哒嗪基甲基 |
344 | CH3 | CH3 | 2-吡嗪基甲基 |
345 | CH3 | CH3 | 5-氯吡嗪-2-基甲基 |
346 | CH3 | CH3 | 6-氯吡嗪-2-基甲基 |
347 | CH3 | CH3 | 3-哒嗪基甲基 |
348 | CH3 | CH3 | 6-氯哒嗪-3-基甲基 |
349 | CH3 | CH3 | 1,3,5-三嗪基甲基 |
350 | CH3 | CH3 | 2-呋喃基甲基 |
351 | CH3 | CH3 | 3-呋喃基甲基 |
352 | CH3 | CH3 | 4-溴呋喃-2-基甲基 |
353 | CH3 | CH3 | 5-氯呋喃-2-基甲基 |
354 | CH3 | CH3 | 2-噻吩基甲基 |
355 | CH3 | CH3 | 3-噻吩基甲基 |
356 | CH3 | CH3 | 5-甲基噻吩-3-基甲基 |
357 | CH3 | CH3 | 5-氯噻吩-2-基甲基 |
358 | CH3 | CH3 | 2-氯噻吩-4-基甲基 |
No. | R3 | R4 | R5 |
359 | CH3 | CH3 | 2-吡咯基甲基 |
360 | CH3 | CH3 | 3-吡咯基甲基 |
361 | CH3 | CH3 | 2-噁唑基甲基 |
362 | CH3 | CH3 | 4-甲基噁唑-2-基甲基 |
363 | CH3 | CH3 | 5-甲基噁唑-2-基甲基 |
364 | CH3 | CH3 | 4-氯噁唑-2-基甲基 |
365 | CH3 | CH3 | 5-氯噁唑-2-基甲基 |
366 | CH3 | CH3 | 4-噁唑基甲基 |
367 | CH3 | CH3 | 2-甲基噁唑-4-基甲基 |
368 | CH3 | CH3 | 5-甲基噁唑-4-基甲基 |
369 | CH3 | CH3 | 2-氯噁唑-4-基甲基 |
370 | CH3 | CH3 | 5-氯噁唑-4-基甲基 |
371 | CH3 | CH3 | 5-噁唑基甲基 |
372 | CH3 | CH3 | 2-甲基噁唑-5-基甲基 |
373 | CH3 | CH3 | 4-甲基噁唑-5-基甲基 |
374 | CH3 | CH3 | 2-氯噁唑-5-基甲基 |
375 | CH3 | CH3 | 4-氯噁唑-5-基甲基 |
376 | CH3 | CH3 | 2-噻唑基甲基 |
377 | CH3 | CH3 | 4-甲基噻唑-2-基甲基 |
378 | CH3 | CH3 | 5-甲基噻唑-2-基甲基 |
No. | R3 | R4 | R5 |
379 | CH3 | CH3 | 4-氯噻唑-2-基甲基 |
380 | CH3 | CH3 | 5-氯噻唑-2-基甲基 |
381 | CH3 | CH3 | 4-噻唑基甲基 |
382 | CH3 | CH3 | 2-甲基噻唑-4-基甲基 |
383 | CH3 | CH3 | 5-甲基噻唑-4-基甲基 |
384 | CH3 | CH3 | 2-氯噻唑-4-基甲基 |
385 | CH3 | CH3 | 5-氯噻唑-4-基甲基 |
386 | CH3 | CH3 | 5-噻唑基甲基 |
387 | CH3 | CH3 | 2-甲基噻唑-5-基甲基 |
388 | CH3 | CH3 | 4-甲基噻唑-5-基甲基 |
389 | CH3 | CH3 | 2-氯噻唑-5-基甲基 |
390 | CH3 | CH3 | 4-氯噻唑-5-基甲基 |
391 | CH3 | CH3 | 3-异噁唑基甲基 |
392 | CH3 | CH3 | 4-甲基异噁唑-3-基甲基 |
393 | CH3 | CH3 | 5-甲基异噁唑-3-基甲基 |
394 | CH3 | CH3 | 4-氯异噁唑-3-基甲基 |
395 | CH3 | CH3 | 5-氯异噁唑-3-基甲基 |
396 | CH3 | CH3 | 4-异噁唑基甲基 |
397 | CH3 | CH3 | 3-甲基异噁唑-4-基甲基 |
398 | CH3 | CH3 | 5-甲基异噁唑-4-基甲基 |
No. | R3 | R4 | R5 |
399 | CH3 | CH3 | 3-氯异噁唑-4-基甲基 |
400 | CH3 | CH3 | 5-氯异噁唑-4-基甲基 |
401 | CH3 | CH3 | 5-异噁唑基甲基 |
402 | CH3 | CH3 | 3-甲基异噁唑-5-基甲基 |
403 | CH3 | CH3 | 4-甲基异噁唑-5-基甲基 |
404 | CH3 | CH3 | 3-氯异噁唑-5-基甲基 |
405 | CH3 | CH3 | 4-氯异噁唑-5-基甲基 |
406 | CH3 | CH3 | 3-异噻唑基甲基 |
407 | CH3 | CH3 | 4-甲基异噻唑-3-基甲基 |
408 | CH3 | CH3 | 5-甲基异噻唑-3-基甲基 |
409 | CH3 | CH3 | 4-氯异噻唑-3-基甲基 |
410 | CH3 | CH3 | 5-氯异噻唑-3-基甲基 |
411 | CH3 | CH3 | 4-异噻唑基甲基 |
412 | CH3 | CH3 | 3-甲基异噻唑-4-基甲基 |
413 | CH3 | CH3 | 5-甲基异噻唑-4-基甲基 |
414 | CH3 | CH3 | 3-氯异噻唑-4-基甲基 |
415 | CH3 | CH3 | 5-氯异噻唑-4-基甲基 |
416 | CH3 | CH3 | 5-异噻唑基甲基 |
417 | CH3 | CH3 | 3-甲基异噻唑-5-基甲基 |
418 | CH3 | CH3 | 4-甲基异噻唑-5-基甲基 |
No. | R3 | R4 | R5 |
419 | CH3 | CH3 | 3-氯异噻唑-5-基甲基 |
420 | CH3 | CH3 | 4-氯异噻唑-5-基甲基 |
421 | CH3 | CH3 | 4-咪唑基甲基 |
422 | CH3 | CH3 | 1-苯基吡唑-3-基甲基 |
423 | CH3 | CH3 | 1-甲基咪唑-4-基甲基 |
424 | CH3 | CH3 | 1-苯基-1,2,4-三唑-3-基甲基 |
425 | CH3 | CH3 | 1,2,4-噁二唑-3-基甲基 |
426 | CH3 | CH3 | 5-氯-1,2,4-噁二唑-3-基甲基 |
427 | CH3 | CH3 | 5-甲基-1,2,4-噁二唑-3-基甲基 |
428 | CH3 | CH3 | 5-三氟甲基-1,2,4-噁二唑-3-基甲基 |
429 | CH3 | CH3 | 1,3,4-噁二唑-2-基甲基 |
430 | CH3 | CH3 | 5-氯-1,3,4-噁二唑-2-基甲基 |
431 | CH3 | CH3 | 5-甲基-1,3,4-噁二唑-2-基甲基 |
432 | CH3 | CH3 | 5-甲氧基-1,3,4-噁二唑-2-基甲基 |
433 | CH3 | CH3 | 1,2,4-噻二唑-3-基甲基 |
434 | CH3 | CH3 | 5-氯-1,2,4-噻二唑-3-基甲基 |
435 | CH3 | CH3 | 5-甲基-1,2,4-噻二唑-3-基甲基 |
436 | CH3 | CH3 | 1,3,4-噻二唑-2-基甲基 |
437 | CH3 | CH3 | 5-氯-1,3,4-噻二唑-2-基甲基 |
438 | CH3 | CH3 | 5-甲基-1,3,4-噻二唑-2-基甲基 |
No. | R3 | R4 | R5 |
439 | CH3 | CH3 | 5-氰基-1,3,4-噻二唑-2-基甲基 |
440 | CH3 | CH3 | 2-(2′-吡啶基氧)乙-1-基 |
441 | CH3 | CH3 | 2-(3′-吡啶基氧)乙-1-基 |
442 | CH3 | CH3 | 2-(4′-吡啶基氧)乙-1-基 |
443 | CH3 | CH3 | 2-(2′-嘧啶基氧)乙-1-基 |
444 | CH3 | CH3 | 2-(4′-嘧啶基氧)乙-1-基 |
445 | CH3 | CH3 | 2-(5′-嘧啶基氧)乙-1-基 |
446 | CH3 | CH3 | 2-(2’-吡嗪基氧)乙-1-基 |
447 | CH3 | CH3 | 2-(2′-哒嗪基氧)乙-1-基 |
448 | CH3 | CH3 | 2-(3′-哒嗪基氧)乙-1-基 |
449 | CH3 | CH3 | 2-(1’3’,5’-三嗪基氧)乙-1-基 |
450 | CH3 | CH3 | 2-(5’-甲基异噁唑-3’-基氧)乙-1-基 |
451 | CH3 | CH3 | 2-(5’-氯异噁唑-3’-基氧)乙-1-基 |
452 | CH3 | CH3 | 2-(2’-甲氧基噻唑-4’-基氧)乙-1-基 |
453 | CH3 | CH3 | 2-(4’-氯噁唑-2’-基氧)乙-1-基 |
454 | CH3 | CH3 | 2-(1′-苯基-1’H-1’,2’,4’-三唑-3’-基氧)乙-1-基 |
455 | CH3 | CH3 | 2-(1’-苯基吡唑-3’-基氧)乙-1-基 |
456 | CH3 | CH3 | C6H5 |
457 | CH3 | CH3 | 2-Cl-C6H4 |
458 | CH3 | CH3 | 3-Cl-C6H4 |
No. | R3 | R4 | R5 |
459 | CH3 | CH3 | 4-Cl-C6H4 |
460 | CH3 | CH3 | 2,3-Cl2-C6H3 |
461 | CH3 | CH3 | 2,4-Cl2-C6H3 |
462 | CH3 | CH3 | 2,5-Cl2-C6H3 |
463 | CH3 | CH3 | 3,4-Cl2-C6H3 |
464 | CH3 | CH3 | 3,5-Cl2-C6H3 |
465 | CH3 | CH3 | 4-CN-C6H4 |
466 | CH3 | CH3 | 2-NO2-C6H4 |
467 | CH3 | CH3 | 3-NO2-C6H4 |
468 | CH3 | CH3 | 4-NO2-C6H4 |
469 | CH3 | CH3 | 2,4-(NO2)2-C6H3 |
470 | CH3 | CH3 | 2-CH3-C6H4 |
471 | CH3 | CH3 | 3-CH3-C6H4 |
472 | CH3 | CH3 | 4-CH3-C6H4 |
473 | CH3 | CH3 | 2,3-(CH3)2-C6H3 |
474 | CH3 | CH3 | 2,4-(CH3)2-C6H3 |
475 | CH3 | CH3 | 2,5-(CH3)2-C6H3 |
476 | CH3 | CH3 | 2,6-(CH3)2-C6H3 |
477 | CH3 | CH3 | 2-C6H5-C6H4 |
478 | CH3 | CH3 | 3-C6H5-C6H4 |
No. | R3 | R4 | R5 |
479 | CH3 | CH3 | 4-C6H5-C6H4 |
480 | CH3 | CH3 | 3-OCH3-C6H4 |
481 | CH3 | CH3 | 4-OCH3-C6H4 |
482 | CH3 | CH3 | 3-乙酰基-C6H4 |
483 | CH3 | CH3 | 4-乙酰基-C6H4 |
484 | CH3 | CH3 | 3-甲氧羰基-C6H4 |
485 | CH3 | CH3 | 4-甲氧羰基-C6H4 |
486 | CH3 | CH3 | 3-CF3-C6H4 |
487 | CH3 | CH3 | 4-CF3-C6H4 |
488 | CH3 | CH3 | 2-萘基 |
489 | CH3 | CH3 | 6-氯哒嗪-3-基 |
490 | CH3 | CH3 | 5-氯吡嗪-2-基 |
491 | CH3 | CH3 | 喹啉-2-基 |
492 | CH3 | CH3 | 2,5-二甲基吡嗪-3-基 |
493 | CH3 | CH3 | 吡嗪-2-基 |
494 | CH3 | CH3 | 3-氯吡啶-2-基 |
495 | CH3 | CH3 | 6-氯吡啶-2-基 |
496 | CH3 | CH3 | 4-三氟甲基,6-氯吡啶-2-基 |
497 | CH3 | CH3 | 4-三氟甲基吡啶-2-基 |
498 | CH3 | CH3 | 6-三氟甲基吡啶-2-基 |
No. | R3 | R4 | R5 |
499 | CH3 | CH3 | 6-甲氧基吡啶-2-基 |
500 | CH3 | CH3 | 5-氯吡啶-2-基 |
501 | CH3 | CH3 | 吡啶-2-基 |
502 | CH3 | CH3 | 苯并噻唑-2-基 |
503 | CH3 | CH3 | 7-氯喹啉-4-基 |
504 | CH3 | CH3 | 3-硝基吡啶-2-基 |
505 | CH3 | CH3 | 吡咯-3-基 |
506 | CH3 | CH3 | 吡咯-2-基 |
507 | CH3 | CH3 | 2,6-二辛基吡啶-4-基 |
508 | CH3 | CH3 | 5-硝基吡啶-2-基 |
509 | CH3 | CH3 | 吡啶-4-基 |
510 | CH3 | CH3 | 吡啶-3-基 |
511 | CH3 | CH3 | 嘧啶-2-基 |
512 | CH3 | CH3 | 嘧啶-4-基 |
513 | CH3 | CH3 | 喹唑啉-4-基 |
514 | CH3 | CH3 | 6-氯嘧啶-4-基 |
515 | CH3 | CH3 | 6-甲氧基嘧啶-4-基 |
516 | CH3 | CH3 | 2,5,6-三氯嘧啶-4-基 |
517 | CH3 | CH3 | 2.6-二甲基嘧啶-4-基 |
518 | CH3 | CH3 | 2-甲基,6-氯嘧啶-4-基 |
No. | R3 | R4 | R5 |
519 | CH3 | CH3 | 2-甲基,6-乙氧基嘧啶-4-基 |
520 | CH3 | CH3 | 4,5,6-三氯嘧啶-2-基 |
521 | CH3 | CH3 | 4,6-二甲氧基嘧啶-2-基 |
522 | CH3 | CH3 | 4,6-二甲基嘧啶-2-基 |
523 | CH3 | CH3 | 4,6-二氯嘧啶-2-基 |
524 | CH3 | CH3 | 4-甲基,6-甲氧基嘧啶-2-基 |
525 | CH3 | CH3 | 4-氯,6-甲氧基嘧啶-2-基 |
526 | CH3 | CH3 | 6-氯喹喔啉-2-基 |
527 | CH3 | CH3 | 3,6-二氯-1,2,4-三嗪-5-基 |
528 | CH3 | CH3 | 4-甲氧基-1,3,5-三嗪-2-基 |
529 | CH3 | CH3 | 4-乙氧基-1,3,5-三嗪-2-基 |
530 | CH3 | CH3 | 4,6-二氯-1,3,5-三嗪-2-基 |
531 | CH3 | CH3 | 4-乙氧基,6-氯-1,3,5-三嗪-2-基 |
532 | CH3 | CH3 | 异噁唑-3-基 |
533 | CH3 | CH3 | 噻吩-2-基 |
534 | CH3 | CH3 | 呋喃-2-基 |
535 | CH3 | CH3 | 噻三唑-5-基 |
536 | CH3 | CH3 | (E)-1-氯丙烯-3-基 |
537 | CH3 | CH3 | (E)-4-(4’-氯苯基)-丁-2-烯-1-基 |
538 | CH3 | CH3 | 丙炔-3-基 |
No. | R3 | R4 | R5 |
539 | CH3 | CH3 | 甲羰基 |
540 | CH3 | CH3 | 乙羰基 |
541 | CH3 | CH3 | n-丙羰基 |
542 | CH3 | CH3 | i-丙羰基 |
543 | CH3 | CH3 | n-丁羰基 |
544 | CH3 | CH3 | s-丁羰基 |
545 | CH3 | CH3 | i-丁羰基 |
546 | CH3 | CH3 | t-丁羰基 |
547 | CH3 | CH3 | n-戊羰基 |
548 | CH3 | CH3 | i-戊羰基 |
549 | CH3 | CH3 | 新-戊羰基 |
550 | CH3 | CH3 | n-己羰基 |
551 | CH3 | CH3 | n-辛羰基 |
552 | CH3 | CH3 | 1-丙烯基羰基 |
553 | CH3 | CH3 | 2-戊烯-1-基-羰基 |
554 | CH3 | CH3 | 2,5-庚二烯-1-基羰基 |
555 | CH3 | CH3 | 苯甲酰基 |
556 | CH3 | CH3 | 2-氯苯甲酰基 |
557 | CH3 | CH3 | 3-氯苯甲酰基 |
558 | CH3 | CH3 | 4-氯苯甲酰基 |
No. | R3 | R4 | R5 |
559 | CH3 | CH3 | 2-氰基苯甲酰基 |
560 | CH3 | CH3 | 3-氰基苯甲酰基 |
561 | CH3 | CH3 | 4-氰基苯甲酰基 |
562 | CH3 | CH3 | 4-甲氧基苯甲酰基 |
563 | CH3 | CH3 | 2-吡啶基羰基 |
564 | CH3 | CH3 | 3-吡啶基羰基 |
565 | CH3 | CH3 | 4-吡啶基羰基 |
566 | CH3 | CH3 | 2-嘧啶基羰基 |
567 | CH3 | CH3 | 2-噁唑基羰基 |
568 | CH3 | CH3 | 4-甲基异噁唑-5-基羰基 |
569 | CH3 | CH3 | 甲基磺酰基 |
570 | CH3 | CH3 | 乙基磺酰基 |
571 | CH3 | CH3 | n-丙基磺酰基 |
572 | CH3 | CH3 | i-丙基磺酰基 |
573 | CH3 | CH3 | n-丁基磺酰基 |
574 | CH3 | CH3 | t-丁基磺酰基 |
575 | CH3 | CH3 | n-戊基磺酰基 |
576 | CH3 | CH3 | 新-戊基磺酰基 |
577 | CH3 | CH3 | n-己基磺酰基 |
578 | CH3 | CH3 | n-辛基磺酰基 |
No. | R3 | R4 | R5 |
579 | CH3 | CH3 | 苯基磺酰基 |
580 | CH3 | CH3 | 2-氯苯磺酰基 |
581 | CH3 | CH3 | 3-氯苯磺酰基 |
582 | CH3 | CH3 | 4-氯苯磺酰基 |
583 | CH3 | CH3 | 2-氰基苯磺酰基 |
584 | CH3 | CH3 | 3-氰基苯磺酰基 |
585 | CH3 | CH3 | 4-氰基苯磺酰基 |
586 | CH3 | CH3 | 2-吡啶基磺酰基 |
587 | CH3 | CH3 | 3-吡啶基磺酰基 |
588 | CH3 | CH3 | 4-吡啶基磺酰基 |
589 | CH3 | CH3 | 2-嘧啶基磺酰基 |
590 | CH3 | CH3 | 4-噁唑基磺酰基 |
591 | CH3 | CH3 | 5-氯噻唑-2-基磺酰基 |
592 | CH3 | CH3 | 2-t-C4H9-C6H4-CH2 |
593 | CH3 | CH3 | 3-t-C4H9-C6H4-CH2 |
594 | CH3 | CH3 | 4-t-C4H9-C6H4-CH2 |
595 | CH3 | CH3 | 2-(4’-氯噻唑-2’-基氧)乙-1-基 |
596 | CH3 | CH3 | 2-(1’-甲基吡唑-4’-基氧)乙-1-基 |
597 | CH3 | CH3 | 4-Br-C6H4 |
598 | CH3 | CH3 | 3,5-(CH3)2-C6H3 |
No. | R3 | R4 | R5 |
599 | CH3 | CH3 | 4-C2H5-C6H4 |
600 | CH3 | CH3 | 3-二甲氨基羰基-C6H4 |
601 | CH3 | CH3 | 4-二甲氨基羰基-C6H4 |
602 | CH3 | CH3 | 2-羟基丙-1-基 |
603 | CH3 | CH3 | 6-羟基-2-甲基嘧啶-4-基甲基 |
604 | CH3 | CH3 | [6-OH,2-CH(CH3)2-嘧啶-4-基]-CH2 |
605 | CH3 | CH3 | [6-OH,2-CH(CH2)2-嘧啶-4-基]-CH2 |
606 | CH3 | CH3 | 5-(2’-呋喃)-戊-1-基 |
607 | CH3 | CH3 | 5-(2’-N-甲基吡咯)-戊-1-基 |
608 | CH3 | CH3 | [2-(4-Cl-C6H4)-噁唑-4-基]-CH2 |
609 | CH3 | CH3 | 3-CF3-吡啶-2-基 |
610 | CH3 | CH3 | 5-CF3-吡啶-2-基 |
611 | CH3 | CH3 | 6-(2’-噻吩基)己-1-基 |
612 | CH3 | t-C4H9 | H |
613 | CH3 | t-C4H9 | CH3 |
614 | CH3 | t-C4H9 | C2H5 |
615 | CH3 | t-C4H9 | n-C3H7 |
616 | CH3 | t-C4H9 | i-C3H7 |
617 | CH3 | t-C4H9 | 环丙基 |
618 | CH3 | t-C4H9 | n-C4H9 |
No. | R3 | R4 | R5 |
619 | CH3 | t-C4H9 | t-C4H9 |
620 | CH3 | t-C4H9 | n-C6H13 |
621 | CH3 | t-C4H9 | (E)-1-氯丙烯-3-基 |
622 | CH3 | t-C4H9 | 丙炔-3-基 |
623 | CH3 | t-C4H9 | 3-甲基丁-2-烯-1-基 |
624 | CH3 | t-C4H9 | 2-萘基-CH2 |
625 | CH3 | t-C4H9 | 4-Cl-C6H4-CH2 |
626 | CH3 | t-C4H9 | (E)-4-(4’-氯苯基)丁-2-烯-1-基 |
627 | CH3 | t-C4H9 | 6-(4’-氯苯基)己-1-基 |
628 | CH3 | t-C4H9 | 3-CF3-C6H4 |
629 | CH3 | C6H5 | H |
630 | CH3 | C6H5 | CH3 |
631 | CH3 | C6H5 | C2H5 |
632 | CH3 | C6H5 | n-C3H7 |
633 | CH3 | C6H5 | i-C3H7 |
634 | CH3 | C6H5 | 环丙基 |
635 | CH3 | C6H5 | n-C4H9 |
636 | CH3 | C6H5 | t-C4H9 |
637 | CH3 | C6H5 | n-C6H13 |
638 | CH3 | C6H5 | 4-Cl-C6H4-CH2 |
No. | R3 | R4 | R5 |
639 | CH3 | C6H5 | 3-CF3-C6H4 |
640 | CH3 | C6H5 | 6-(4’-氯苯基)己-1-基 |
641 | CH3 | C6H5 | (E)-4-(4’-氯苯基)丁-2-烯-1-基 |
642 | CH3 | H | H |
643 | CH3 | H | CH3 |
644 | CH3 | H | C2H5 |
645 | CH3 | H | n-C3H7 |
646 | CH3 | H | i-C3H7 |
647 | CH3 | OH | H |
648 | CH3 | OH | CH3 |
649 | CH3 | OH | C2H5 |
650 | CH3 | OH | n-C3H7 |
651 | CH3 | OH | i-C3H7 |
652 | CH3 | Cl | CH3 |
653 | CH3 | Cl | C2H5 |
654 | CH3 | Cl | n-C3H7 |
655 | CH3 | Cl | i-C3H7 |
656 | CH3 | OCH3 | H |
657 | CH3 | OCH3 | CH3 |
658 | CH3 | OCH3 | C2H5 |
No. | R3 | R4 | R5 |
659 | CH3 | OCH3 | n-C3H7 |
660 | CH3 | OCH3 | i-C3H7 |
661 | CH3 | SCH3 | H |
662 | CH3 | SCH3 | CH3 |
663 | CH3 | SCH3 | C2H5 |
664 | CH3 | SCH3 | n-C3H7 |
665 | CH3 | SCH3 | i-C3H7 |
666 | CH3 | 环丙基 | H |
667 | CH3 | 环丙基 | CH3 |
668 | CH3 | 环丙基 | C2H5 |
669 | CH3 | 环丙基 | n-C3H7 |
670 | CH3 | 环丙基 | i-C3H7 |
671 | CH3 | 2-吡啶基 | H |
672 | CH3 | 2-吡啶基 | CH3 |
673 | CH3 | 2-吡啶基 | C2H5 |
674 | CH3 | 2-吡啶基 | n-C3H7 |
675 | CH3 | 2-吡啶基 | i-C3H7 |
676 | CH3 | 3-吡啶基 | H |
677 | CH3 | 3-吡啶基 | CH3 |
678 | CH3 | 3-吡啶基 | C2H5 |
No. | R3 | R4 | R5 |
679 | CH3 | 3-吡啶基 | n-C3H7 |
680 | CH3 | 3-吡啶基 | i-C3H7 |
681 | CH3 | 4-吡啶基 | H |
682 | CH3 | 4-吡啶基 | CH3 |
683 | CH3 | 4-吡啶基 | C2H5 |
684 | CH3 | 4-吡啶基 | n-C3H7 |
685 | CH3 | 4-吡啶基 | i-C3H7 |
686 | CH3 | 2-嘧啶基 | H |
687 | CH3 | 2-嘧啶基 | CH3 |
688 | CH3 | 2-嘧啶基 | C2H5 |
689 | CH3 | 2-嘧啶基 | n-C3H7 |
690 | CH3 | 2-嘧啶基 | i-C3H7 |
691 | CH3 | 4-嘧啶基 | H |
692 | CH3 | 4-嘧啶基 | CH3 |
693 | CH3 | 4-嘧啶基 | C2H5 |
694 | CH3 | 4-嘧啶基 | n-C3H7 |
695 | CH3 | 4-嘧啶基 | i-C3H7 |
696 | CH3 | 5-嘧啶基 | H |
697 | CH3 | 5-嘧啶基 | CH3 |
698 | CH3 | 5-嘧啶基 | C2H5 |
No. | R3 | R4 | R5 |
699 | CH3 | 5-嘧啶基 | n-C3H7 |
700 | CH3 | 5-嘧啶基 | i-C3H7 |
701 | CH3 | 1,3,5-三嗪基 | H |
702 | CH3 | 1,3,5-三嗪基 | CH3 |
703 | CH3 | 1,3,5-三嗪基 | C2H5 |
704 | CH3 | 1,3,5-三嗪基 | n-C3H7 |
705 | CH3 | 1,3,5-三嗪基 | i-C3H7 |
706 | CH3 | 2-呋喃基 | H |
707 | CH3 | 2-呋喃基 | CH3 |
708 | CH3 | 2-呋喃基 | C2H5 |
709 | CH3 | 2-呋喃基 | n-C3H7 |
710 | CH3 | 2-呋喃基 | i-C3H7 |
711 | CH3 | 3-呋喃基 | H |
712 | CH3 | 3-呋喃基 | CH3 |
713 | CH3 | 3-呋喃基 | C2H5 |
714 | CH3 | 3-呋喃基 | n-C3H7 |
715 | CH3 | 3-呋喃基 | i-C3H7 |
716 | CH3 | 2-噻吩基 | H |
717 | CH3 | 2-噻吩基 | CH3 |
718 | CH3 | 2-噻吩基 | C2H5 |
No. | R3 | R4 | R5 |
719 | CH3 | 2-噻吩基 | n-C3H7 |
720 | CH3 | 2-噻吩基 | i-C3H7 |
721 | CH3 | 3-噻吩基 | H |
722 | CH3 | 3-噻吩基 | CH3 |
723 | CH3 | 3-噻吩基 | C2H5 |
724 | CH3 | 3-噻吩基 | n-C3H7 |
725 | CH3 | 3-噻吩基 | i-C3H7 |
726 | CH3 | 2-噁唑基 | H |
727 | CH3 | 2-噁唑基 | CH3 |
728 | CH3 | 2-噁唑基 | C2H5 |
729 | CH3 | 2-噁唑基 | n-C3H7 |
730 | CH3 | 2-噁唑基 | i-C3H7 |
731 | CH3 | 4-噁唑基 | H |
732 | CH3 | 4-噁唑基 | CH3 |
733 | CH3 | 4-噁唑基 | C2H5 |
734 | CH3 | 4-噁唑基 | n-C3H7 |
735 | CH3 | 4-噁唑基 | i-C3H7 |
736 | CH3 | 2-噻唑基 | H |
737 | CH3 | 2-噻唑基 | CH3 |
738 | CH3 | 2-噻唑基 | C2H5 |
No. | R3 | R4 | R5 |
739 | CH3 | 2-噻唑基 | n-C3H7 |
740 | CH3 | 2-噻唑基 | i-C3H7 |
741 | CH3 | 4-噻唑基 | H |
742 | CH3 | 4-噻唑基 | CH3 |
743 | CH3 | 4-噻唑基 | C2H5 |
744 | CH3 | 4-噻唑基 | n-C3H7 |
745 | CH3 | 4-噻唑基 | i-C3H7 |
746 | CH3 | 3-异噁唑基 | H |
747 | CH3 | 3-异噁唑基 | CH3 |
748 | CH3 | 3-异噁唑基 | C2H5 |
749 | CH3 | 3-异噁唑基 | n-C3H7 |
750 | CH3 | 3-异噁唑基 | i-C3H7 |
751 | CH3 | 5-异噁唑基 | H |
752 | CH3 | 5-异噁唑基 | CH3 |
753 | CH3 | 5-异噁唑基 | C2H5 |
754 | CH3 | 5-异噁唑基 | n-C3H7 |
755 | CH3 | 5-异噁唑基 | i-C3H7 |
756 | CH3 | 2-咪唑基 | H |
757 | CH3 | 2-咪唑基 | CH3 |
758 | CH3 | 2-咪唑基 | C2H5 |
No. | R3 | R4 | R5 |
759 | CH3 | 2-咪唑基 | n-C3H7 |
760 | CH3 | 2-咪唑基 | i-C3H7 |
761 | CH3 | 3-吡唑基 | H |
762 | CH3 | 3-吡唑基 | CH3 |
763 | CH3 | 3-吡唑基 | C2H5 |
764 | CH3 | 3-吡唑基 | n-C3H7 |
765 | CH3 | 3-吡唑基 | i-C3H7 |
766 | CH3 | 4-吡唑基 | H |
767 | CH3 | 4-吡唑基 | CH3 |
768 | CH3 | 4-吡唑基 | C2H5 |
769 | CH3 | 4-吡唑基 | n-C3H7 |
770 | CH3 | 4-吡唑基 | i-C3H7 |
771 | OCH3 | H | H |
772 | OCH3 | H | CH3 |
773 | OCH3 | H | C2H5 |
774 | OCH3 | H | n-C3H7 |
775 | OCH3 | H | i-C3H7 |
776 | OCH3 | OH | H |
777 | OCH3 | OH | CH3 |
778 | OCH3 | OH | C2H5 |
No. | R3 | R4 | R5 |
779 | OCH3 | OH | n-C3H7 |
780 | OCH3 | OH | i-C3H7 |
781 | OCH3 | Cl | n-C4H9 |
782 | OCH3 | Cl | CH3 |
783 | OCH3 | Cl | C2H5 |
784 | OCH3 | Cl | n-C3H7 |
785 | OCH3 | Cl | i-C3H7 |
786 | OCH3 | OCH3 | H |
787 | OCH3 | OCH3 | CH3 |
788 | OCH3 | OCH3 | C2H5 |
789 | OCH3 | OCH3 | n-C3H7 |
790 | OCH3 | OCH3 | i-C3H7 |
791 | OCH3 | SCH3 | H |
792 | OCH3 | SCH3 | CH3 |
793 | OCH3 | SCH3 | C2H5 |
794 | OCH3 | SCH3 | n-C3H7 |
795 | OCH3 | SCH3 | i-C3H7 |
796 | OCH3 | CH3 | H |
797 | OCH3 | CH3 | CH3 |
798 | OCH3 | CH3 | C2H5 |
No. | R3 | R4 | R5 |
799 | OCH3 | CH3 | n-C3H7 |
800 | OCH3 | CH3 | i-C3H7 |
801 | OCH3 | 环丙基 | H |
802 | OCH3 | 环丙基 | CH3 |
803 | OCH3 | 环丙基 | C2H5 |
804 | OCH3 | 环丙基 | n-C3H7 |
805 | OCH3 | 环丙基 | i-C3H7 |
806 | OCH3 | 2-吡啶基 | H |
807 | OCH3 | 2-吡啶基 | CH3 |
808 | OCH3 | 2-吡啶基 | C2H5 |
809 | OCH3 | 2-吡啶基 | n-C3H7 |
810 | OCH3 | 2-吡啶基 | i-C3H7 |
811 | OCH3 | 3-吡啶基 | H |
812 | OCH3 | 3-吡啶基 | CH3 |
813 | OCH3 | 3-吡啶基 | C2H5 |
814 | OCH3 | 3-吡啶基 | n-C3H7 |
815 | OCH3 | 3-吡啶基 | i-C3H7 |
816 | OCH3 | 4-吡啶基 | H |
817 | OCH3 | 4-吡啶基 | CH3 |
818 | OCH3 | 4-吡啶基 | C2H5 |
No. | R3 | R4 | R5 |
819 | OCH3 | 4-吡啶基 | n-C3H7 |
820 | OCH3 | 4-嘧啶基 | i-C3H7 |
821 | OCH3 | 2-嘧啶基 | H |
822 | OCH3 | 2-嘧啶基 | CH3 |
823 | OCH3 | 2-嘧啶基 | C2H5 |
824 | OCH3 | 2-嘧啶基 | n-C3H7 |
825 | OCH3 | 2-嘧啶基 | i-C3H7 |
826 | OCH3 | 4-嘧啶基 | H |
827 | OCH3 | 4-嘧啶基 | CH3 |
828 | OCH3 | 4-嘧啶基 | C2H5 |
829 | OCH3 | 4-嘧啶基 | n-C3H7 |
830 | OCH3 | 4-嘧啶基 | i-C3H7 |
831 | OCH3 | 5-嘧啶基 | H |
832 | OCH3 | 5-嘧啶基 | CH3 |
833 | OCH3 | 5-嘧啶基 | C2H5 |
834 | OCH3 | 5-嘧啶基 | n-C3H7 |
835 | OCH3 | 5-嘧啶基 | i-C3H7 |
836 | OCH3 | 1,3,5-三嗪基 | H |
837 | OCH3 | 1,3,5-三嗪基 | CH3 |
838 | OCH3 | 1,3,5-三嗪基 | C2H5 |
No. | R3 | R4 | R5 |
839 | OCH3 | 1,3,5-三嗪基 | n-C3H7 |
840 | OCH3 | 1,3,5-三嗪基 | i-C3H7 |
841 | OCH3 | 2-呋喃基 | H |
842 | OCH3 | 2-呋喃基 | CH3 |
843 | OCH3 | 2-呋喃基 | C2H5 |
844 | OCH3 | 2-呋喃基 | n-C3H7 |
845 | OCH3 | 2-呋喃基 | i-C3H7 |
846 | OCH3 | 3-呋喃基 | H |
847 | OCH3 | 3-呋喃基 | CH3 |
848 | OCH3 | 3-呋喃基 | C2H5 |
849 | OCH3 | 3-呋喃基 | n-C3H7 |
850 | OCH3 | 3-呋喃基 | i-C3H7 |
851 | OCH3 | 2-噻吩基 | H |
852 | OCH3 | 2-噻吩基 | CH3 |
853 | OCH3 | 2-噻吩基 | C2H5 |
854 | OCH3 | 2-噻吩基 | n-C3H7 |
855 | OCH3 | 2-噻吩基 | i-C3H7 |
856 | OCH3 | 3-噻吩基 | H |
857 | OCH3 | 3-噻吩基 | CH3 |
858 | OCH3 | 3-噻吩基 | C2H5 |
No. | R3 | R4 | R5 |
859 | OCH3 | 3-噻吩基 | n-C3H7 |
860 | OCH3 | 3-噻吩基 | i-C3H7 |
861 | OCH3 | 2-噁唑基 | H |
862 | OCH3 | 2-噁唑基 | CH3 |
863 | OCH3 | 2-噁唑基 | C2H5 |
864 | OCH3 | 2-噁唑基 | n-C3H7 |
865 | OCH3 | 2-噁唑基 | i-C3H7 |
866 | OCH3 | 4-噁唑基 | H |
867 | OCH3 | 4-噁唑基 | CH3 |
868 | OCH3 | 4-噁唑基 | C2H5 |
869 | OCH3 | 4-噁唑基 | n-C3H7 |
870 | OCH3 | 4-噁唑基 | i-C3H7 |
871 | OCH3 | 2-噻唑基 | H |
872 | OCH3 | 2-噻唑基 | CH3 |
873 | OCH3 | 2-噻唑基 | C2H5 |
874 | OCH3 | 2-噻唑基 | n-C3H7 |
875 | OCH3 | 2-噻唑基 | i-C3H7 |
876 | OCH3 | 4-噻唑基 | H |
877 | OCH3 | 4-噻唑基 | CH3 |
878 | OCH3 | 4-噻唑基 | C2H5 |
No. | R3 | R4 | R5 |
879 | OCH3 | 4-噻唑基 | n-C3H7 |
880 | OCH3 | 4-噻唑基 | i-C3H7 |
881 | OCH3 | 3-异噁唑基 | H |
882 | OCH3 | 3-异噁唑基 | CH3 |
883 | OCH3 | 3-异噁唑基 | C2H5 |
884 | OCH3 | 3-异噁唑基 | n-C3H7 |
885 | OCH3 | 3-异噁唑基 | i-C3H7 |
886 | OCH3 | 5-异噁唑基 | H |
887 | OCH3 | 5-异噁唑基 | CH3 |
888 | OCH3 | 5-异噁唑基 | C2H5 |
889 | OCH3 | 5-异噁唑基 | n-C3H7 |
890 | OCH3 | 5-异噁唑基 | i-C3H7 |
891 | OCH3 | 2-咪唑基 | H |
892 | OCH3 | 2-咪唑基 | CH3 |
893 | OCH3 | 2-咪唑基 | C2H5 |
894 | OCH3 | 2-咪唑基 | n-C3H7 |
895 | OCH3 | 2-咪唑基 | i-C3H7 |
896 | OCH3 | 3-吡唑基 | H |
897 | OCH3 | 3-吡唑基 | CH3 |
898 | OCH3 | 3-吡唑基 | C2H5 |
No. | R3 | R4 | R5 |
899 | OCH3 | 3-吡唑基 | n-C3H7 |
900 | OCH3 | 3-吡唑基 | i-C3H7 |
901 | OCH3 | 4-吡唑基 | H |
902 | OCH3 | 4-吡唑基 | CH3 |
903 | OCH3 | 4-吡唑基 | C2H5 |
904 | OCH3 | 4-吡唑基 | n-C3H7 |
905 | OCH3 | 4-吡唑基 | i-C3H7 |
906 | OH | H | H |
907 | OH | H | CH3 |
908 | OH | H | C2H5 |
909 | OH | H | n-C3H7 |
910 | OH | H | i-C3H7 |
911 | OH | OH | H |
912 | OH | OH | CH3 |
913 | OH | OH | C2H5 |
914 | OH | OH | n-C3H7 |
915 | OH | OH | i-C3H7 |
916 | OH | Cl | n-C4H9 |
917 | OH | Cl | CH3 |
918 | OH | Cl | C2H5 |
No. | R3 | R4 | R5 |
919 | OH | Cl | n-C3H7 |
920 | OH | Cl | i-C3H7 |
921 | OH | OCH3 | H |
922 | OH | OCH3 | CH3 |
923 | OH | OCH3 | C2H5 |
924 | OH | OCH3 | n-C3H7 |
925 | OH | OCH3 | i-C3H7 |
926 | OH | SCH3 | H |
927 | OH | SCH3 | CH3 |
928 | OH | SCH3 | C2H5 |
929 | OH | SCH3 | n-C3H7 |
930 | OH | SCH3 | i-C3H7 |
931 | OH | CH3 | H |
932 | OH | CH3 | CH3 |
933 | OH | CH3 | C2H5 |
934 | OH | CH3 | n-C3H7 |
935 | OH | CH3 | i-C3H7 |
936 | OH | 环丙基 | H |
937 | OH | 环丙基 | CH3 |
938 | OH | 环丙基 | C2H5 |
No. | R3 | R4 | R5 |
939 | OH | 环丙基 | n-C3H7 |
940 | OH | 环丙基 | i-C3H7 |
941 | OH | 2-吡啶基 | H |
942 | OH | 2-吡啶基 | CH3 |
943 | OH | 2-吡啶基 | C2H5 |
944 | OH | 2-吡啶基 | n-C3H7 |
945 | OH | 2-吡啶基 | i-C3H7 |
946 | OH | 3-吡啶基 | H |
947 | OH | 3-吡啶基 | CH3 |
948 | OH | 3-吡啶基 | C2H5 |
949 | OH | 3-吡啶基 | n-C3H7 |
950 | OH | 3-吡啶基 | i-C3H7 |
951 | OH | 4-吡啶基 | H |
952 | OH | 4-吡啶基 | CH3 |
953 | OH | 4-吡啶基 | C2H5 |
954 | OH | 4-吡啶基 | n-C3H7 |
955 | OH | 4-吡啶基 | i-C3H7 |
956 | OH | 2-嘧啶基 | H |
957 | OH | 2-嘧啶基 | CH3 |
958 | OH | 2-嘧啶基 | C2H5 |
No. | R3 | R4 | R5 |
959 | OH | 2-嘧啶基 | n-C3H7 |
960 | OH | 2-嘧啶基 | i-C3H7 |
961 | OH | 4-嘧啶基 | H |
962 | OH | 4-嘧啶基 | CH3 |
963 | OH | 4-嘧啶基 | C2H5 |
964 | OH | 4-嘧啶基 | n-C3H7 |
965 | OH | 4-嘧啶基 | i-C3H7 |
966 | OH | 5-嘧啶基 | H |
967 | OH | 5-嘧啶基 | CH3 |
968 | OH | 5-嘧啶基 | C2H5 |
969 | OH | 5-嘧啶基 | n-C3H7 |
970 | OH | 5-嘧啶基 | i-C3H7 |
971 | OH | 1,3,5-三嗪基 | H |
972 | OH | 1,3,5-三嗪基 | CH3 |
973 | OH | 1,3,5-三嗪基 | C2H5 |
974 | OH | 1,3,5-三嗪基 | n-C3H7 |
975 | OH | 1,3,5-三嗪基 | i-C3H7 |
976 | OH | 2-呋喃基 | H |
977 | OH | 2-呋喃基 | CH3 |
978 | OH | 2-呋喃基 | C2H5 |
No. | R3 | R4 | R5 |
979 | OH | 2-呋喃基 | n-C3H7 |
980 | OH | 2-呋喃基 | i-C3H7 |
981 | OH | 3-呋喃基 | H |
982 | OH | 3-呋喃基 | CH3 |
983 | OH | 3-呋喃基 | C2H5 |
984 | OH | 3-呋喃基 | n-C3H7 |
985 | OH | 3-呋喃基 | i-C3H7 |
986 | OH | 2-噻吩基 | H |
987 | OH | 2-噻吩基 | CH3 |
988 | OH | 2-噻吩基 | C2H5 |
989 | OH | 2-噻吩基 | n-C3H7 |
990 | OH | 2-噻吩基 | i-C3H7 |
991 | OH | 3-噻吩基 | H |
992 | OH | 3-噻吩基 | CH3 |
993 | OH | 3-噻吩基 | C2H5 |
994 | OH | 3-噻吩基 | n-C3H7 |
995 | OH | 3-噻吩基 | i-C3H7 |
996 | OH | 2-噁唑基 | H |
997 | OH | 2-噁唑基 | CH3 |
998 | OH | 2-噁唑基 | C2H5 |
No. | R3 | R4 | R5 |
999 | OH | 2-噁唑基 | n-C3H7 |
1000 | OH | 2-噁唑基 | i-C3H7 |
1001 | OH | 4-噁唑基 | H |
1002 | OH | 4-噁唑基 | CH3 |
1003 | OH | 4-噁唑基 | C2H5 |
1004 | OH | 4-噁唑基 | n-C3H7 |
1005 | OH | 2-噻唑基 | i-C3H7 |
1006 | OH | 2-噻唑基 | H |
1007 | OH | 2-噻唑基 | CH3 |
1008 | OH | 2-噻唑基 | C2H5 |
1009 | OH | 2-噻唑基 | n-C3H7 |
1010 | OH | 2-噻唑基 | i-C3H7 |
1011 | OH | 4-噻唑基 | H |
1012 | OH | 4-噻唑基 | CH3 |
1013 | OH | 4-噻唑基 | C2H5 |
1014 | OH | 4-异噁唑基 | n-C3H7 |
1015 | OH | 4-异噁唑基 | i-C3H7 |
1016 | OH | 3-异噁唑基 | H |
1017 | OH | 3-异噁唑基 | CH3 |
1018 | OH | 3-异噁唑基 | C2H5 |
No. | R3 | R4 | R5 |
1019 | OH | 3-异噁唑基 | n-C3H7 |
1020 | OH | 3-异噁唑基 | i-C3H7 |
1021 | OH | 5-异噁唑基 | H |
1022 | OH | 5-异噁唑基 | CH3 |
1023 | OH | 5-异噁唑基 | C2H5 |
1024 | OH | 5-异噁唑基 | n-C3H7 |
1025 | OH | 5-异噁唑基 | i-C3H7 |
1026 | OH | 2-咪唑基 | H |
1027 | OH | 2-咪唑基 | CH3 |
1028 | OH | 2-咪唑基 | C2H5 |
1029 | OH | 2-咪唑基 | n-C3H7 |
1030 | OH | 2-咪唑基 | i-C3H7 |
1031 | OH | 3-吡唑基 | H |
1032 | OH | 3-吡唑基 | CH3 |
1033 | OH | 3-吡唑基 | C2H5 |
1034 | OH | 3-吡唑基 | n-C3H7 |
1035 | OH | 3-吡唑基 | i-C3H7 |
1036 | OH | 4-吡唑基 | H |
1037 | OH | 4-吡唑基 | CH3 |
1038 | OH | 4-吡唑基 | C2H5 |
No. | R3 | R4 | R5 |
1039 | OH | 4-吡唑基 | n-C3H7 |
1040 | OH | 4-吡唑基 | i-C3H7 |
1041 | H | H | H |
1042 | H | H | CH3 |
1043 | H | H | C2H5 |
1044 | H | H | n-C3H7 |
1045 | H | H | i-C3H7 |
1046 | H | OH | H |
1047 | H | OH | CH3 |
1048 | H | OH | C2H5 |
1049 | H | OH | n-C3H7 |
1050 | H | OH | i-C3H7 |
1051 | H | Cl | n-C4H9 |
1052 | H | Cl | CH3 |
1053 | H | Cl | C2H5 |
1054 | H | Cl | n-C3H7 |
1055 | H | Cl | i-C3H7 |
1056 | H | OCH3 | H |
1057 | H | OCH3 | CH3 |
1058 | H | OCH3 | C2H5 |
No. | R3 | R4 | R5 |
1059 | H | OCH3 | n-C3H7 |
1060 | H | OCH3 | i-C3H7 |
1061 | H | CH3 | H |
1062 | H | CH3 | CH3 |
1063 | H | CH3 | C2H5 |
1064 | H | CH3 | n-C3H7 |
1065 | H | CH3 | i-C3H7 |
1066 | H | 环丙基 | H |
1067 | H | 环丙基 | CH3 |
1068 | H | 环丙基 | C2H5 |
1069 | H | 环丙基 | n-C3H7 |
1070 | H | 环丙基 | i-C3H7 |
1071 | Cl | H | H |
1072 | Cl | H | CH3 |
1073 | Cl | H | C2H5 |
1074 | Cl | H | n-C3H7 |
1075 | Cl | H | i-C3H7 |
1076 | Cl | OH | H |
1077 | Cl | OH | CH3 |
1078 | Cl | OH | C2H5 |
No. | R3 | R4 | R5 |
1079 | Cl | OH | n-C3H7 |
1080 | Cl | OH | i-C3H7 |
1081 | Cl | Cl | n-C4H9 |
1082 | Cl | Cl | CH3 |
1083 | Cl | Cl | C2H5 |
1084 | Cl | Cl | n-C3H7 |
1085 | Cl | Cl | i-C3H7 |
1086 | Cl | OCH3 | H |
1087 | Cl | OCH3 | CH3 |
1088 | Cl | OCH3 | C2H5 |
1089 | Cl | OCH3 | n-C3H7 |
1090 | Cl | OCH3 | i-C3H7 |
1091 | Cl | CH3 | H |
1092 | Cl | CH3 | CH3 |
1093 | Cl | CH3 | C2H5 |
1094 | Cl | CH3 | n-C3H7 |
1095 | Cl | CH3 | i-C3H7 |
1096 | Cl | 环丙基 | H |
1097 | Cl | 环丙基 | CH3 |
1098 | Cl | 环丙基 | C2H5 |
No. | R3 | R4 | R5 |
1099 | Cl | 环丙基 | n-C3H7 |
1100 | Cl | 环丙基 | i-C3H7 |
1101 | SCH3 | H | H |
1102 | SCH3 | H | CH3 |
1103 | SCH3 | H | C2H5 |
1104 | SCH3 | H | n-C3H7 |
1105 | SCH3 | H | i-C3H7 |
1106 | SCH3 | OH | H |
1107 | SCH3 | OH | CH3 |
1108 | SCH3 | OH | C2H5 |
1109 | SCH3 | OH | n-C3H7 |
1110 | SCH3 | OH | i-C3H7 |
1111 | SCH3 | CH3 | H |
1112 | SCH3 | CH3 | CH3 |
1113 | SCH3 | CH3 | C2H5 |
1114 | SCH3 | CH3 | n-C3H7 |
1115 | SCH3 | CH3 | i-C3H7 |
1116 | SCH3 | SCH3 | H |
1117 | SCH3 | SCH3 | CH3 |
1118 | SCH3 | SCH3 | C2H5 |
No. | R3 | R4 | R5 |
1119 | SCH3 | SCH3 | n-C3H7 |
1120 | SCH3 | SCH3 | i-C3H7 |
1121 | SCH3 | 环丙基 | H |
1122 | SCH3 | 环丙基 | CH3 |
1123 | SCH3 | 环丙基 | C2H5 |
1124 | SCH3 | 环丙基 | n-C3H7 |
1125 | SCH3 | 环丙基 | i-C3H7 |
1126 | 环丙基 | H | H |
1127 | 环丙基 | H | CH3 |
1128 | 环丙基 | H | C2H5 |
1129 | 环丙基 | H | n-C3H7 |
1130 | 环丙基 | H | i-C3H7 |
1131 | 环丙基 | OH | H |
1132 | 环丙基 | OH | CH3 |
1133 | 环丙基 | OH | C2H5 |
1134 | 环丙基 | OH | n-C3H7 |
1135 | 环丙基 | OH | i-C3H7 |
1136 | 环丙基 | Cl | n-C4H9 |
1137 | 环丙基 | Cl | CH3 |
1138 | 环丙基 | Cl | C2H5 |
No. | R3 | R4 | R5 |
1139 | 环丙基 | Cl | n-C3H7 |
1140 | 环丙基 | Cl | i-C3H7 |
1141 | 环丙基 | OCH3 | H |
1142 | 环丙基 | OCH3 | CH3 |
1143 | 环丙基 | OCH3 | C2H5 |
1144 | 环丙基 | OCH3 | n-C3H7 |
1145 | 环丙基 | OCH3 | i-C3H7 |
1146 | 环丙基 | SCH3 | H |
1147 | 环丙基 | SCH3 | CH3 |
1148 | 环丙基 | SCH3 | C2H5 |
1149 | 环丙基 | SCH3 | n-C3H7 |
1150 | 环丙基 | SCH3 | i-C3H7 |
1151 | 环丙基 | CH3 | H |
1152 | 环丙基 | CH3 | CH3 |
1153 | 环丙基 | CH3 | C2H5 |
1154 | 环丙基 | CH3 | n-C3H7 |
1155 | 环丙基 | CH3 | i-C3H7 |
1156 | CH3 | 2-F-C6H4 | H |
1157 | CH3 | 2-F-C6H4 | CH3 |
1158 | CH3 | 2-F-C6H4 | C2H5 |
No. | R3 | R4 | R5 |
1159 | CH3 | 2-F-C6H4 | n-C3H7 |
1160 | CH3 | 2-F-C6H4 | i-C3H7 |
1161 | CH3 | 2-F-C6H4 | n-C4H9 |
1162 | CH3 | 2-F-C6H4 | t-C4H9 |
1163 | CH3 | 2-F-C6H4 | n-C6H13 |
1164 | CH3 | 2-F-C6H4 | 丙-1-烯-3-基 |
1165 | CH3 | 2-F-C6H4 | (E)-1-氯丙-1-烯-3-基 |
1166 | CH3 | 2-F-C6H4 | 丙炔-3-基 |
1167 | CH3 | 2-F-C6H4 | 3-甲基-丁-2-烯-1-基 |
1168 | CH3 | 3-F-C6H4 | H |
1169 | CH3 | 3-F-C6H4 | CH3 |
1170 | CH3 | 3-F-C6H4 | C2H5 |
1171 | CH3 | 3-F-C6H4 | n-C3H7 |
1172 | CH3 | 3-F-C6H4 | i-C3H7 |
1173 | CH3 | 3-F-C6H4 | n-C4H9 |
1174 | CH3 | 3-F-C6H4 | t-C4H9 |
1175 | CH3 | 3-F-C6H4 | n-C6H13 |
1176 | CH3 | 3-F-C6H4 | 丙-1-烯-3-基 |
1177 | CH3 | 3-F-C6H4 | (E)-1-氯丙-1-烯-3-基 |
1178 | CH3 | 3-F-C6H4 | 丙炔-3-基 |
No. | R3 | R4 | R5 |
1179 | CH3 | 3-F-C6H4 | 3-甲基-丁-2-烯-1-基 |
1180 | CH3 | 4-F-C6H4 | H |
1181 | CH3 | 4-F-C6H4 | CH3 |
1182 | CH3 | 4-F-C6H4 | C2H5 |
1183 | CH3 | 4-F-C6H4 | n-C3H7 |
1184 | CH3 | 4-F-C6H4 | i-C3H7 |
1185 | CH3 | 4-F-C6H4 | n-C4H9 |
1186 | CH3 | 4-F-C6H4 | t-C4H9 |
1187 | CH3 | 4-F-C6H4 | n-C6H13 |
1188 | CH3 | 4-F-C6H4 | 丙-1-烯-3-基 |
1189 | CH3 | 4-F-C6H4 | (E)-1-氯丙-1-烯-3-基 |
1190 | CH3 | 4-F-C6H4 | 丙炔-3-基 |
1191 | CH3 | 4-F-C6H4 | 3-甲基-丁-2-烯-1-基 |
1192 | CH3 | 2-Cl-C6H4 | H |
1193 | CH3 | 2-Cl-C6H4 | CH3 |
1194 | CH3 | 2-Cl-C6H4 | C2H5 |
1195 | CH3 | 2-Cl-C6H4 | n-C3H7 |
1196 | CH3 | 2-Cl-C6H4 | i-C3H7 |
1197 | CH3 | 2-Cl-C6H4 | n-C4H9 |
1198 | CH3 | 2-Cl-C6H4 | t-C4H9 |
No. | R3 | R4 | R5 |
1199 | CH3 | 2-Cl-C6H4 | n-C6H13 |
1200 | CH3 | 2-Cl-C6H4 | 丙-1-烯-3-基 |
1201 | CH3 | 2-Cl-C6H4 | (E)-1-氯丙-1-烯-3-基 |
1202 | CH3 | 2-Cl-C6H4 | 丙炔-3-基 |
1203 | CH3 | 2-Cl-C6H4 | 3-甲基-丁-2-烯-1-基 |
1204 | CH3 | 3-Cl-C6H4 | H |
1205 | CH3 | 3-Cl-C6H4 | CH3 |
1206 | CH3 | 3-Cl-C6H4 | C2H5 |
1207 | CH3 | 3-Cl-C6H4 | n-C3H7 |
1208 | CH3 | 3-Cl-C6H4 | i-C3H7 |
1209 | CH3 | 3-Cl-C6H4 | n-C4H9 |
1210 | CH3 | 3-Cl-C6H4 | t-C4H9 |
1211 | CH3 | 3-Cl-C6H4 | n-C6H13 |
1212 | CH3 | 3-Cl-C6H4 | 丙-1-烯-3-基 |
1213 | CH3 | 3-Cl-C6H4 | (E)-1-氯丙-1-烯-3-基 |
1214 | CH3 | 3-Cl-C6H4 | 丙炔-3-基 |
1215 | CH3 | 3-Cl-C6H4 | 3-甲基-丁-2-烯-1-基 |
1216 | CH3 | 4-Cl-C6H4 | H |
1217 | CH3 | 4-Cl-C6H4 | CH3 |
1218 | CH3 | 4-Cl-C6H4 | C2H5 |
No. | R3 | R4 | R5 |
1219 | CH3 | 4-Cl-C6H4 | n-C3H7 |
1220 | CH3 | 4-Cl-C6H4 | i-C3H7 |
1221 | CH3 | 4-Cl-C6H4 | n-C4H9 |
1222 | CH3 | 4-Cl-C6H4 | t-C4H9 |
1223 | CH3 | 4-Cl-C6H4 | n-C6H13 |
1224 | CH3 | 4-Cl-C6H4 | 丙-1-烯-3-基 |
1225 | CH3 | 4-Cl-C6H4 | (E)-1-氯丙-1-烯-3-基 |
1226 | CH3 | 4-Cl-C6H4 | 丙炔-3-基 |
1227 | CH3 | 4-Cl-C6H4 | 3-甲基-丁-2-烯-1-基 |
1228 | CH3 | 2,3-Cl2-C6H3 | H |
1229 | CH3 | 2,3-Cl2-C6H3 | CH3 |
1230 | CH3 | 2,3-Cl2-C6H3 | C2H5 |
1231 | CH3 | 2,3-Cl2-C6H3 | n-C3H7 |
1232 | CH3 | 2,3-Cl2-C6H3 | i-C3H7 |
1233 | CH3 | 2,3-Cl2-C6H3 | n-C4H9 |
1234 | CH3 | 2,3-Cl2-C6H3 | t-C4H9 |
1235 | CH3 | 2,3-Cl2-C6H3 | n-C6H13 |
1236 | CH3 | 2,3-Cl2-C6H3 | 丙-1-烯-3-基 |
1237 | CH3 | 2,3-Cl2-C6H3 | (E)-1-氯丙-1-烯-3-基 |
1238 | CH3 | 2,3-Cl2-C6H3 | 丙炔-3-基 |
No. | R3 | R4 | R5 |
1239 | CH3 | 2,3-C12-C6H3 | 3-甲基-丁-2-烯-1-基 |
1240 | CH3 | 2,4-Cl2-C6H3 | H |
1241 | CH3 | 2,4-Cl2-C6H3 | CH3 |
1242 | CH3 | 2,4-Cl2-C6H3 | C2H5 |
1243 | CH3 | 2,4-Cl2-C6H3 | n-C3H7 |
1244 | CH3 | 2,4-Cl2-C6H3 | i-C3H7 |
1245 | CH3 | 2,4-Cl2-C6H3 | n-C4H9 |
1246 | CH3 | 2,4-Cl2-C6H3 | t-C4H9 |
1247 | CH3 | 2,4-Cl2-C6H3 | n-C6H13 |
1248 | CH3 | 2,4-Cl2-C6H3 | 丙-1-烯-3-基 |
1249 | CH3 | 2,4-Cl2-C6H3 | (E)-1-氯丙-1-烯-3-基 |
1250 | CH3 | 2,4-Cl2-C6H3 | 丙炔-3-基 |
1251 | CH3 | 2,4-Cl2-C6H3 | 3-甲基-丁-2-烯-1-基 |
1252 | CH3 | 2,5-Cl2-C6H3 | H |
1253 | CH3 | 2,5-Cl2-C6H3 | CH3 |
1254 | CH3 | 2,5-Cl2-C6H3 | C2H5 |
1255 | CH3 | 2,5-Cl2-C6H3 | n-C3H7 |
1256 | CH3 | 2,5-Cl2-C6H3 | i-C3H7 |
1257 | CH3 | 2,5-Cl2-C6H3 | n-C4H9 |
1258 | CH3 | 2,5-Cl2-C6H3 | t-C4H9 |
No. | R3 | R4 | R5 |
1259 | CH3 | 2,5-Cl2-C6H3 | n-C6H13 |
1260 | CH3 | 2,5-Cl2-C6H3 | 丙-1-烯-3-基 |
1261 | CH3 | 2,5-Cl2-C6H3 | (E)-1-氯丙-1-烯-3-基 |
1262 | CH3 | 2,5-Cl2-C6H3 | 丙炔-3-基 |
1263 | CH3 | 2,5-Cl2-C6H3 | 3-甲基-丁-2-烯-1-基 |
1264 | CH3 | 2,6-Cl2-C6H3 | H |
1265 | CH3 | 2,6-Cl2-C6H3 | CH3 |
1266 | CH3 | 2,6-Cl2-C6H3 | C2H5 |
1267 | CH3 | 2,6-Cl2-C6H3 | n-C3H7 |
1268 | CH3 | 2,6-Cl2-C6H3 | i-C3H7 |
1269 | CH3 | 2,6-Cl2-C6H3 | n-C4H9 |
1270 | CH3 | 2,6-Cl2-C6H3 | t-C4H9 |
1271 | CH3 | 2,6-Cl2-C6H3 | n-C6H13 |
1272 | CH3 | 2,6-Cl2-C6H3 | 丙-1-烯-3-基 |
1273 | CH3 | 2,6-Cl2-C6H3 | (E)-1-氯丙-1-烯-3-基 |
1274 | CH3 | 2,6-Cl2-C6H3 | 丙炔-3-基 |
1275 | CH3 | 2,6-Cl2-C6H3 | 3-甲基-丁-2-烯-1-基 |
1276 | CH3 | 3,4-Cl2-C6H3 | H |
1277 | CH3 | 3,4-Cl2-C6H3 | CH3 |
1278 | CH3 | 3,4-Cl2-C6H3 | C2H5 |
No. | R3 | R4 | R5 |
1279 | CH3 | 3,4-Cl2-C6H3 | n-C3H7 |
1280 | CH3 | 3,4-Cl2-C6H3 | i-C3H7 |
1281 | CH3 | 3,4-Cl2-C6H3 | n-C4H9 |
1282 | CH3 | 3,4-Cl2-C6H3 | t-C4H9 |
1283 | CH3 | 3,4-Cl2-C6H3 | n-C6H13 |
1284 | CH3 | 3,4-Cl2-C6H3 | 丙-1-烯-3-基 |
1285 | CH3 | 3,4-Cl2-C6H3 | (E)-1-氯丙-1-烯-3-基 |
1286 | CH3 | 3,4-Cl2-C6H3 | 丙炔-3-基 |
1287 | CH3 | 3,4-Cl2-C6H3 | 3-甲基-丁-2-烯-1-基 |
1288 | CH3 | 3,5-Cl2-C6H3 | H |
1289 | CH3 | 3,5-Cl2-C6H3 | CH3 |
1290 | CH3 | 3,5-Cl2-C6H3 | C2H5 |
1291 | CH3 | 3,5-Cl2-C6H3 | n-C3H7 |
1292 | CH3 | 3,5-Cl2-C6H3 | i-C3H7 |
1293 | CH3 | 3,5-Cl2-C6H3 | n-C4H9 |
1294 | CH3 | 3,5-Cl2-C6H3 | t-C4H9 |
1295 | CH3 | 3,5-Cl2-C6H3 | n-C6H13 |
1296 | CH3 | 3,5-Cl2-C6H3 | 丙-1-烯-3-基 |
1297 | CH3 | 3,5-Cl2-C6H3 | (E)-1-氯丙-1-烯-3-基 |
1298 | CH3 | 3,5-Cl2-C6H3 | 丙炔-3-基 |
No. | R3 | R4 | R5 |
1299 | CH3 | 3,5-Cl2-C6H3 | 3-甲基-丁-2-烯-1-基 |
1300 | CH3 | 2-Br-C6H4 | H |
1301 | CH3 | 2-Br-C6H4 | CH3 |
1302 | CH3 | 2-Br-C6H4 | C2H5 |
1303 | CH3 | 2-Br-C6H4 | n-C3H7 |
1304 | CH3 | 2-Br-C6H4 | i-C3H7 |
1305 | CH3 | 2-Br-C6H4 | n-C4H9 |
1306 | CH3 | 2-Br-C6H4 | t-C4H9 |
1307 | CH3 | 2-Br-C6H4 | n-C6H13 |
1308 | CH3 | 2-Br-C6H4 | 丙-1-烯-3-基 |
1309 | CH3 | 2-Br-C6H4 | (E)-1-氯丙-1-烯-3-基 |
1310 | CH3 | 2-Br-C6H4 | 丙炔-3-基 |
1311 | CH3 | 2-Br-C6H4 | 3-甲基-丁-2-烯-1-基 |
1312 | CH3 | 3-Br-C6H4 | H |
1313 | CH3 | 3-Br-C6H4 | CH3 |
1314 | CH3 | 3-Br-C6H4 | C2H5 |
1315 | CH3 | 3-Br-C6H4 | n-C3H7 |
1316 | CH3 | 3-Br-C6H4 | i-C3H7 |
1317 | CH3 | 3-Br-C6H4 | n-C4H9 |
1318 | CH3 | 3-Br-C6H4 | t-C4H9 |
No. | R3 | R4 | R5 |
1319 | CH3 | 3-Br-C6H4 | n-C6H13 |
1320 | CH3 | 3-Br-C6H4 | 丙-1-烯-3-基 |
1321 | CH3 | 3-Br-C6H4 | (E)-1-氯丙-1-烯-3-基 |
1322 | CH3 | 3-Br-C6H4 | 丙炔-3-基 |
1323 | CH3 | 3-Br-C6H4 | 3-甲基-丁-2-烯-1-基 |
1324 | CH3 | 4-Br-C6H4 | H |
1325 | CH3 | 4-Br-C6H4 | CH3 |
1326 | CH3 | 4-Br-C6H4 | C2H5 |
1327 | CH3 | 4-Br-C6H4 | n-C3H7 |
1328 | CH3 | 4-Br-C6H4 | i-C3H7 |
1329 | CH3 | 4-Br-C6H4 | n-C4H9 |
1330 | CH3 | 4-Br-C6H4 | t-C4H9 |
1331 | CH3 | 4-Br-C6H4 | n-C6H13 |
1332 | CH3 | 4-Br-C6H4 | 丙-1-烯-3-基 |
1333 | CH3 | 4-Br-C6H4 | (E)-1-氯丙-1-烯-3-基 |
1334 | CH3 | 4-Br-C6H4 | 丙炔-3-基 |
1335 | CH3 | 4-Br-C6H4 | 3-甲基-丁-2-烯-1-基 |
1336 | CH3 | 2-I-C6H4 | H |
1337 | CH3 | 2-I-C6H4 | CH3 |
1338 | CH3 | 2-I-C6H4 | C2H5 |
No. | R3 | R4 | R5 |
1339 | CH3 | 2-I-C6H4 | n-C3H7 |
1340 | CH3 | 2-I-C6H4 | i-C3H7 |
1341 | CH3 | 2-I-C6H4 | n-C4H9 |
1342 | CH3 | 2-I-C6H4 | t-C4H9 |
1343 | CH3 | 2-I-C6H4 | n-C6H13 |
1344 | CH3 | 2-I-C6H4 | 丙-1-烯-3-基 |
1345 | CH3 | 2-I-C6H4 | (E)-1-氯丙-1-烯-3-基 |
1346 | CH3 | 2-I-C6H4 | 丙炔-3-基 |
1347 | CH3 | 2-I-C6H4 | 3-甲基-丁-2-烯-1-基 |
1348 | CH3 | 3-I-C6H4 | H |
1349 | CH3 | 3-I-C6H4 | CH3 |
1350 | CH3 | 3-I-C6H4 | C2H5 |
1351 | CH3 | 3-I-C6H4 | n-C3H7 |
1352 | CH3 | 3-I-C6H4 | i-C3H7 |
1353 | CH3 | 3-I-C6H4 | n-C4H9 |
1354 | CH3 | 3-I-C6H4 | t-C4H9 |
1355 | CH3 | 3-I-C6H4 | n-C6H13 |
1356 | CH3 | 3-I-C6H4 | 丙-1-烯-3-基 |
1357 | CH3 | 3-I-C6H4 | (E)-1-氯丙-1-烯-3-基 |
1358 | CH3 | 3-I-C6H4 | 丙炔-3-基 |
No. | R3 | R4 | R5 |
1359 | CH3 | 3-I-C6H4 | 3-甲基-丁-2-烯-1-基 |
1360 | CH3 | 4-I-C6H4 | H |
1361 | CH3 | 4-I-C6H4 | CH3 |
1362 | CH3 | 4-I-C6H4 | C2H5 |
1363 | CH3 | 4-I-C6H4 | n-C3H7 |
1364 | CH3 | 4-I-C6H4 | i-C3H7 |
1365 | CH3 | 4-I-C6H4 | n-C4H9 |
1366 | CH3 | 4-I-C6H4 | t-C4H9 |
1367 | CH3 | 4-I-C6H4 | n-C6H13 |
1368 | CH3 | 4-I-C6H4 | 丙-1-烯-3-基 |
1369 | CH3 | 4-I-C6H4 | (E)-1-氯丙-1-烯-3-基 |
1370 | CH3 | 4-I-C6H4 | 丙炔-3-基 |
1371 | CH3 | 4-I-C6H4 | 3-甲基-丁-2-烯-1-基 |
1372 | CH3 | 2-CN-C6H4 | H |
1373 | CH3 | 2-CN-C6H4 | CH3 |
1374 | CH3 | 2-CN-C6H4 | C2H5 |
1375 | CH3 | 2-CN-C6H4 | n-C3H7 |
1376 | CH3 | 2-CN-C6H4 | i-C3H7 |
1377 | CH3 | 2-CN-C6H4 | n-C4H9 |
1378 | CH3 | 2-CN-C6H4 | t-C4H9 |
No. | R3 | R4 | R5 |
1379 | CH3 | 2-CN-C6H4 | n-C6H13 |
1380 | CH3 | 2-CN-C6H4 | 丙-1-烯-3-基 |
1381 | CH3 | 2-CN-C6H4 | (E)-1-氯丙-1-烯-3-基 |
1382 | CH3 | 2-CN-C6H4 | 丙炔-3-基 |
1383 | CH3 | 2-CN-C6H4 | 3-甲基-丁-2-烯-1-基 |
1384 | CH3 | 3-CN-C6H4 | H |
1385 | CH3 | 3-CN-C6H4 | CH3 |
1386 | CH3 | 3-CN-C6H4 | C2H5 |
1387 | CH3 | 3-CN-C6H4 | n-C3H7 |
1388 | CH3 | 3-CN-C6H4 | i-C3H7 |
1389 | CH3 | 3-CN-C6H4 | n-C4H9 |
1390 | CH3 | 3-CN-C6H4 | t-C4H9 |
1391 | CH3 | 3-CN-C6H4 | n-C6H13 |
1392 | CH3 | 3-CN-C6H4 | 丙-1-烯-3-基 |
1393 | CH3 | 3-CN-C6H4 | (E)-1-氯丙-1-烯-3-基 |
1394 | CH3 | 3-CN-C6H4 | 丙炔-3-基 |
1395 | CH3 | 3-CN-C6H4 | 3-甲基-丁-2-烯-1-基 |
1396 | CH3 | 4-CN-C6H4 | H |
1397 | CH3 | 4-CN-C6H4 | CH3 |
1398 | CH3 | 4-CN-C6H4 | C2H5 |
No. | R3 | R4 | R5 |
1399 | CH3 | 4-CN-C6H4 | n-C3H7 |
1400 | CH3 | 4-CN-C6H4 | i-C3H7 |
1401 | CH3 | 4-CN-C6H4 | n-C4H9 |
1402 | CH3 | 4-CN-C6H4 | t-C4H9 |
1403 | CH3 | 4-CN-C6H4 | n-C6H13 |
1404 | CH3 | 4-CN-C6H4 | 丙-1-烯-3-基 |
1405 | CH3 | 4-CN-C6H4 | (E)-1-氯丙-1-烯-3-基 |
1406 | CH3 | 4-CN-C6H4 | 丙炔-3-基 |
1407 | CH3 | 4-CN-C6H4 | 3-甲基-丁-2-烯-1-基 |
1408 | CH3 | 2-NO2-C6H4 | H |
1409 | CH3 | 2-NO2-C6H4 | CH3 |
1410 | CH3 | 2-NO2-C6H4 | C2H5 |
1411 | CH3 | 2-NO2-C6H4 | n-C3H7 |
1412 | CH3 | 2-NO2-C6H4 | i-C3H7 |
1413 | CH3 | 2-NO2-C6H4 | n-C4H9 |
1414 | CH3 | 2-NO2-C6H4 | t-C4H9 |
1415 | CH3 | 2-NO2-C6H4 | n-C6H13 |
1416 | CH3 | 2-NO2-C6H4 | 丙-1-烯-3-基 |
1417 | CH3 | 2-NO2-C6H4 | (E)-1-氯丙-1-烯-3-基 |
1418 | CH3 | 2-NO2-C6H4 | 丙炔-3-基 |
No. | R3 | R4 | R5 |
1419 | CH3 | 2-NO2-C6H4 | 3-甲基-丁-2-烯-1-基 |
1420 | CH3 | 3-NO2-C6H4 | H |
1421 | CH3 | 3-NO2-C6H4 | CH3 |
1422 | CH3 | 3-NO2-C6H4 | C2H5 |
1423 | CH3 | 3-NO2-C6H4 | n-C3H7 |
1424 | CH3 | 3-NO2-C6H4 | i-C3H7 |
1425 | CH3 | 3-NO2-C6H4 | n-C4H9 |
1426 | CH3 | 3-NO2-C6H4 | t-C4H9 |
1427 | CH3 | 3-NO2-C6H4 | n-C6H13 |
1428 | CH3 | 3-NO2-C6H4 | 丙-1-烯-3-基 |
1429 | CH3 | 3-NO2-C6H4 | (E)-1-氯丙-1-烯-3-基 |
1430 | CH3 | 3-NO2-C6H4 | 丙炔-3-基 |
1431 | CH3 | 3-NO2-C6H4 | 3-甲基-丁-2-烯-1-基 |
1432 | CH3 | 4-NO2-C6H4 | H |
1433 | CH3 | 4-NO2-C6H4 | CH3 |
1434 | CH3 | 4-NO2-C6H4 | C2H5 |
1435 | CH3 | 4-NO2-C6H4 | n-C3H7 |
1436 | CH3 | 4-NO2-C6H4 | i-C3H7 |
1437 | CH3 | 4-NO2-C6H4 | n-C4H9 |
1438 | CH3 | 4-NO2-C6H4 | t-C4H9 |
No. | R3 | R4 | R5 |
1439 | CH3 | 4-NO2-C6H4 | n-C6H13 |
1440 | CH3 | 4-NO2-C6H4 | 丙-1-烯-3-基 |
1441 | CH3 | 4-NO2-C6H4 | (E)-1-氯丙-1-烯-3-基 |
1442 | CH3 | 4-NO2-C6H4 | 丙炔-3-基 |
1443 | CH3 | 4-NO2-C6H4 | 3-甲基-丁-2-烯-1-基 |
1444 | CH3 | 2-CH3-C6H4 | H |
1445 | CH3 | 2-CH3-C6H4 | CH3 |
1446 | CH3 | 2-CH3-C6H4 | C2H5 |
1447 | CH3 | 2-CH3-C6H4 | n-C3H7 |
1448 | CH3 | 2-CH3-C6H4 | i-C3H7 |
1449 | CH3 | 2-CH3-C6H4 | n-C4H9 |
1450 | CH3 | 2-CH3-C6H4 | t-C4H9 |
1451 | CH3 | 2-CH3-C6H4 | n-C6H13 |
1452 | CH3 | 2-CH3-C6H4 | 丙-1-烯-3-基 |
1453 | CH3 | 2-CH3-C6H4 | (E)-1-氯丙-1-烯-3-基 |
1454 | CH3 | 2-CH3-C6H4 | 丙炔-3-基 |
1455 | CH3 | 2-CH3-C6H4 | 3-甲基-丁-2-烯-1-基 |
1456 | CH3 | 3-CH3-C6H4 | H |
1457 | CH3 | 3-CH3-C6H4 | CH3 |
1458 | CH3 | 3-CH3-C6H4 | C2H5 |
No. | R3 | R4 | R5 |
1459 | CH3 | 3-CH3-C6H4 | n-C3H7 |
1460 | CH3 | 3-CH3-C6H4 | i-C3H7 |
1461 | CH3 | 3-CH3-C6H4 | n-C4H9 |
1462 | CH3 | 3-CH3-C6H4 | t-C4H9 |
1463 | CH3 | 3-CH3-C6H4 | n-C6H13 |
1464 | CH3 | 3-CH3-C6H4 | 丙-1-烯-3-基 |
1465 | CH3 | 3-CH3-C6H4 | (E)-1-氯丙-1-烯-3-基 |
1466 | CH3 | 3-CH3-C6H4 | 丙炔-3-基 |
1467 | CH3 | 3-CH3-C6H4 | 3-甲基-丁-2-烯-1-基 |
1468 | CH3 | 4-CH3-C6H4 | H |
1469 | CH3 | 4-CH3-C6H4 | CH3 |
1470 | CH3 | 4-CH3-C6H4 | C2H5 |
1471 | CH3 | 4-CH3-C6H4 | n-C3H7 |
1472 | CH3 | 4-CH3-C6H4 | i-C3H7 |
1473 | CH3 | 4-CH3-C6H4 | n-C4H9 |
1474 | CH3 | 4-CH3-C6H4 | t-C4H9 |
1475 | CH3 | 4-CH3-C6H4 | n-C6H13 |
1476 | CH3 | 4-CH3-C6H4 | 丙-1-烯-3-基 |
1477 | CH3 | 4-CH3-C6H4 | (E)-1-氯丙-1-烯-3-基 |
1478 | CH3 | 4-CH3-C6H4 | 丙炔-3-基 |
No. | R3 | R4 | R5 |
1479 | CH3 | 4-CH3-C6H4 | 3-甲基-丁-2-烯-1-基 |
1480 | CH3 | 2,3-(CH3)2-C6H3 | H |
1481 | CH3 | 2,3-(CH3)2-C6H3 | CH3 |
1482 | CH3 | 2,3-(CH3)2-C6H3 | C2H5 |
1483 | CH3 | 2,3-(CH3)2-C6H3 | n-C3H7 |
1484 | CH3 | 2,3-(CH3)2-C6H3 | i-C3H7 |
1485 | CH3 | 2,3-(CH3)2-C6H3 | n-C4H9 |
1486 | CH3 | 2,3-(CH3)2-C6H3 | t-C4H9 |
1487 | CH3 | 2,3-(CH3)2-C6H3 | n-C6H13 |
1488 | CH3 | 2,3-(CH3)2-C6H3 | 丙-1-烯-3-基 |
1489 | CH3 | 2,3-(CH3)2-C6H3 | (E)-1-氯丙-1-烯-3-基 |
1490 | CH3 | 2,3-(CH3)2-C6H3 | 丙炔-3-基 |
1491 | CH3 | 2,3-(CH3)2-C6H3 | 3-甲基-丁-2-烯-1-基 |
1492 | CH3 | 2,4-(CH3)2-C6H3 | H |
1493 | CH3 | 2,4-(CH3)2-C6H3 | CH3 |
1494 | CH3 | 2,4-(CH3)2-C6H3 | C2H5 |
1495 | CH3 | 2,4-(CH3)2-C6H3 | n-C3H7 |
1496 | CH3 | 2,4-(CH3)2-C6H3 | i-C3H7 |
1497 | CH3 | 2,4-(CH3)2-C6H3 | n-C4H9 |
1498 | CH3 | 2,4-(CH3)2-C6H3 | t-C4H9 |
No. | R3 | R4 | R5 |
1499 | CH3 | 2,4-(CH3)2-C6H3 | n-C6H13 |
1500 | CH3 | 2,4-(CH3)2-C6H3 | 丙-1-烯-3-基 |
1501 | CH3 | 2,4-(CH3)2-C6H3 | (E)-1-氯丙-1-烯-3-基 |
1502 | CH3 | 2,4-(CH3)2-C6H3 | 丙炔-3-基 |
1503 | CH3 | 2,4-(CH3)2-C6H3 | 3-甲基-丁-2-烯-1-基 |
1504 | CH3 | 2,5-(CH3)2-C6H3 | H |
1505 | CH3 | 2,5-(CH3)2-C6H3 | CH3 |
1506 | CH3 | 2,5-(CH3)2-C6H3 | C2H5 |
1507 | CH3 | 2,5-(CH3)2-C6H3 | n-C3H7 |
1508 | CH3 | 2,5-(CH3)2-C6H3 | i-C3H7 |
1509 | CH3 | 2,5-(CH3)2-C6H3 | n-C4H9 |
1510 | CH3 | 2,5-(CH3)2-C6H3 | t-C4H9 |
1511 | CH3 | 2,5-(CH3)2-C6H3 | n-C6H13 |
1512 | CH3 | 2,5-(CH3)2-C6H3 | 丙-1-烯-3-基 |
1513 | CH3 | 2,5-(CH3)2-C6H3 | (E)-1-氯丙-1-烯-3-基 |
1514 | CH3 | 2,5-(CH3)2-C6H3 | 丙炔-3-基 |
1515 | CH3 | 2,5-(CH3)2-C6H3 | 3-甲基-丁-2-烯-1-基 |
1516 | CH3 | 2,6-(CH3)2-C6H3 | H |
1517 | CH3 | 2,6-(CH3)2-C6H3 | CH3 |
1518 | CH3 | 2,6-(CH3)2-C6H3 | C2H5 |
No. | R3 | R4 | R5 |
1519 | CH3 | 2,6-(CH3)2-C6H3 | n-C3H7 |
1520 | CH3 | 2,6-(CH3)2-C6H3 | i-C3H7 |
1521 | CH3 | 2,6-(CH3)2-C6H3 | n-C4H9 |
1522 | CH3 | 2,6-(CH3)2-C6H3 | t-C4H9 |
1523 | CH3 | 2,6-(CH3)2-C6H3 | n-C6H13 |
1524 | CH3 | 2,6-(CH3)2-C6H3 | 丙-1-烯-3-基 |
1525 | CH3 | 2,6-(CH3)2-C6H3 | (E)-1-氯丙-1-烯-3-基 |
1526 | CH3 | 2,6-(CH3)2-C6H3 | 丙炔-3-基 |
1527 | CH3 | 2,6-(CH3)2-C6H3 | 3-甲基-丁-2-烯-1-基 |
1528 | CH3 | 3,4-(CH3)2-C6H3 | H |
1529 | CH3 | 3,4-(CH3)2-C6H3 | CH3 |
1530 | CH3 | 3,4-(CH3)2-C6H3 | C2H5 |
1531 | CH3 | 3,4-(CH3)2-C6H3 | n-C3H7 |
1532 | CH3 | 3,4-(CH3)2-C6H3 | i-C3H7 |
1533 | CH3 | 3,4-(CH3)2-C6H3 | n-C4H9 |
1534 | CH3 | 3,4-(CH3)2-C6H3 | t-C4H9 |
1535 | CH3 | 3,4-(CH3)2-C6H3 | n-C6H13 |
1536 | CH3 | 3,4-(CH3)2-C6H3 | 丙-1-烯-3-基 |
1537 | CH3 | 3,4-(CH3)2-C6H3 | (E)-1-氯丙-1-烯-3-基 |
1538 | CH3 | 3,4-(CH3)2-C6H3 | 丙炔-3-基 |
No. | R3 | R4 | R5 |
1539 | CH3 | 3,4-(CH3)2-C6H3 | 3-甲基-丁-2-烯-1-基 |
1540 | CH3 | 3,5-(CH3)2-C6H3 | H |
1541 | CH3 | 3,5-(CH3)2-C6H3 | CH3 |
1542 | CH3 | 3,5-(CH3)2-C6H3 | C2H5 |
1543 | CH3 | 3,5-(CH3)2-C6H3 | n-C3H7 |
1544 | CH3 | 3,5-(CH3)2-C6H3 | i-C3H7 |
1545 | CH3 | 3,5-(CH3)2-C6H3 | n-C4H9 |
1546 | CH3 | 3,5-(CH3)2-C6H3 | t-C4H9 |
1547 | CH3 | 3,5-(CH3)2-C6H3 | n-C6H13 |
1548 | CH3 | 3,5-(CH3)2-C6H3 | 丙-1-烯-3-基 |
1549 | CH3 | 3,5-(CH3)2-C6H3 | (E)-1-氯丙-1-烯-3-基 |
1550 | CH3 | 3,5-(CH3)2-C6H3 | 丙炔-3-基 |
1551 | CH3 | 3,5-(CH3)2-C6H3 | 3-甲基-丁-2-烯-1-基 |
1552 | CH3 | 2-C2H5-C6H4 | H |
1553 | CH3 | 2-C2H5-C6H4 | CH3 |
1554 | CH3 | 2-C2H5-C6H4 | C2H5 |
1555 | CH3 | 2-C2H5-C6H4 | n-C3H7 |
1556 | CH3 | 2-C2H5-C6H4 | i-C3H7 |
1557 | CH3 | 2-C2H5-C6H4 | n-C4H9 |
1558 | CH3 | 2-C2H5-C6H4 | t-C4H9 |
No. | R3 | R4 | R5 |
1559 | CH3 | 2-C2H5-C6H4 | n-C6H13 |
1560 | CH3 | 2-C2H5-C6H4 | 丙-1-烯-3-基 |
1561 | CH3 | 2-C2H5-C6H4 | (E)-1-氯丙-1-烯-3-基 |
1562 | CH3 | 2-C2H5-C6H4 | 丙炔-3-基 |
1563 | CH3 | 2-C2H5-C6H4 | 3-甲基-丁-2-烯-1-基 |
1564 | CH3 | 3-C2H5-C6H4 | H |
1565 | CH3 | 3-C2H5-C6H4 | CH3 |
1566 | CH3 | 3-C2H5-C6H4 | C2H5 |
1567 | CH3 | 3-C2H5-C6H4 | n-C3H7 |
1568 | CH3 | 3-C2H5-C6H4 | i-C3H7 |
1569 | CH3 | 3-C2H5-C6H4 | n-C4H9 |
1570 | CH3 | 3-C2H5-C6H4 | t-C4H9 |
1571 | CH3 | 3-C2H5-C6H4 | n-C6H13 |
1572 | CH3 | 3-C2H5-C6H4 | 丙-1-烯-3-基 |
1573 | CH3 | 3-C2H5-C6H4 | (E)-1-氯丙-1-烯-3-基 |
1574 | CH3 | 3-C2H5-C6H4 | 丙炔-3-基 |
1575 | CH3 | 3-C2H5-C6H4 | 3-甲基-丁-2-烯-1-基 |
1576 | CH3 | 4-C2H5-C6H4 | H |
1577 | CH3 | 4-C2H5-C6H4 | CH3 |
1578 | CH3 | 4-C2H5-C6H4 | C2H5 |
No. | R3 | R4 | R5 |
1579 | CH3 | 4-C2H5-C6H4 | n-C3H7 |
1580 | CH3 | 4-C2H5-C6H4 | i-C3H7 |
1581 | CH3 | 4-C2H5-C6H4 | n-C4H9 |
1582 | CH3 | 4-C2H5-C6H4 | t-C4H9 |
1583 | CH3 | 4-C2H5-C6H4 | n-C6H13 |
1584 | CH3 | 4-C2H5-C6H4 | 丙-1-烯-3-基 |
1585 | CH3 | 4-C2H5-C6H4 | (E)-1-氯丙-1-烯-3-基 |
1586 | CH3 | 4-C2H5-C6H4 | 丙炔-3-基 |
1587 | CH3 | 4-C2H5-C6H4 | 3-甲基-丁-2-烯-1-基 |
1588 | CH3 | 2-i-C3H7-C6H4 | H |
1589 | CH3 | 2-i-C3H7-C6H4 | CH3 |
1590 | CH3 | 2-i-C3H7-C6H4 | C2H5 |
1591 | CH3 | 2-i-C3H7-C6H4 | n-C3H7 |
1592 | CH3 | 2-i-C3H7-C6H4 | i-C3H7 |
1593 | CH3 | 2-i-C3H7-C6H4 | n-C4H9 |
1594 | CH3 | 2-i-C3H7-C6H4 | t-C4H9 |
1595 | CH3 | 2-i-C3H7-C6H4 | n-C6H13 |
1596 | CH3 | 2-i-C3H7-C6H4 | 丙-1-烯-3-基 |
1597 | CH3 | 2-i-C3H7-C6H4 | (E)-1-氯丙-1-烯-3-基 |
1598 | CH3 | 2-i-C3H7-C6H4 | 丙炔-3-基 |
No. | R3 | R4 | R5 |
1599 | CH3 | 2-i-C3H7-C6H4 | 3-甲基-丁-2-烯-1-基 |
1600 | CH3 | 3-i-C3H7-C6H4 | H |
1601 | CH3 | 3-i-C3H7-C6H4 | CH3 |
1602 | CH3 | 3-i-C3H7-C6H4 | C2H5 |
1603 | CH3 | 3-i-C3H7-C6H4 | n-C3H7 |
1604 | CH3 | 3-i-C3H7-C6H4 | i-C3H7 |
1605 | CH3 | 3-i-C3H7-C6H4 | n-C4H9 |
1606 | CH3 | 3-i-C3H7-C6H4 | t-C4H9 |
1607 | CH3 | 3-i-C3H7-C6H4 | n-C6H13 |
1608 | CH3 | 3-i-C3H7-C6H4 | 丙-1-烯-3-基 |
1609 | CH3 | 3-i-C3H7-C6H4 | (E)-1-氯丙-1-烯-3-基 |
1610 | CH3 | 3-i-C3H7-C6H4 | 丙炔-3-基 |
1611 | CH3 | 3-i-C3H7-C6H4 | 3-甲基-丁-2-烯-1-基 |
1612 | CH3 | 4-i-C3H7-C6H4 | H |
1613 | CH3 | 4-i-C3H7-C6H4 | CH3 |
1614 | CH3 | 4-i-C3H7-C6H4 | C2H5 |
1615 | CH3 | 4-i-C3H7-C6H4 | n-C3H7 |
1616 | CH3 | 4-i-C3H7-C6H4 | i-C3H7 |
1617 | CH3 | 4-i-C3H7-C6H4 | n-C4H9 |
1618 | CH3 | 4-i-C3H7-C6H4 | t-C4H9 |
No. | R3 | R4 | R5 |
1619 | CH3 | 4-i-C3H7-C6H4 | n-C6H13 |
1620 | CH3 | 4-i-C3H7-C6H4 | 丙-1-烯-3-基 |
1621 | CH3 | 4-i-C3H7-C6H4 | (E)-1-氯丙-1-烯-3-基 |
1622 | CH3 | 4-i-C3H7-C6H4 | 丙炔-3-基 |
1623 | CH3 | 4-i-C3H7-C6H4 | 3-甲基-丁-2-烯-1-基 |
1624 | CH3 | 2-OH-C6H4 | H |
1625 | CH3 | 2-OH-C6H4 | CH3 |
1626 | CH3 | 2-OH-C6H4 | C2H5 |
1627 | CH3 | 2-OH-C6H4 | n-C3H7 |
1628 | CH3 | 2-OH-C6H4 | i-C3H7 |
1629 | CH3 | 2-OH-C6H4 | n-C4H9 |
1630 | CH3 | 2-OH-C6H4 | t-C4H9 |
1631 | CH3 | 2-OH-C6H4 | n-C6H13 |
1632 | CH3 | 2-OH-C6H4 | 丙-1-烯-3-基 |
1633 | CH3 | 2-OH-C6H4 | (E)-1-氯丙-1-烯-3-基 |
1634 | CH3 | 2-OH-C6H4 | 丙炔-3-基 |
1635 | CH3 | 2-OH-C6H4 | 3-甲基-丁-2-烯-1-基 |
1636 | CH3 | 3-OH-C6H4 | H |
1637 | CH3 | 3-OH-C6H4 | CH3 |
1638 | CH3 | 3-OH-C6H4 | C2H5 |
No. | R3 | R4 | R5 |
1639 | CH3 | 3-OH-C6H4 | n-C3H7 |
1640 | CH3 | 3-OH-C6H4 | i-C3H7 |
1641 | CH3 | 3-OH-C6H4 | n-C4H9 |
1642 | CH3 | 3-OH-C6H4 | t-C4H9 |
1643 | CH3 | 3-OH-C6H4 | n-C6H13 |
1644 | CH3 | 3-OH-C6H4 | 丙-1-烯-3-基 |
1645 | CH3 | 3-OH-C6H4 | (E)-1-氯丙-1-烯-3-基 |
1646 | CH3 | 3-OH-C6H4 | 丙炔-3-基 |
1647 | CH3 | 3-OH-C6H4 | 3-甲基-丁-2-烯-1-基 |
1648 | CH3 | 4-OH-C6H4 | H |
1649 | CH3 | 4-OH-C6H4 | CH3 |
1650 | CH3 | 4-OH-C6H4 | C2H5 |
1651 | CH3 | 4-OH-C6H4 | n-C3H7 |
1652 | CH3 | 4-OH-C6H4 | i-C3H7 |
1653 | CH3 | 4-OH-C6H4 | n-C4H9 |
1654 | CH3 | 4-OH-C6H4 | t-C4H9 |
1655 | CH3 | 4-OH-C6H4 | n-C6H13 |
1656 | CH3 | 4-OH-C6H4 | 3-甲基-丁-2-烯-1-基 |
1657 | CH3 | 4-OH-C6H4 | (E)-1-氯丙-1-烯-3-基 |
1658 | CH3 | 4-OH-C6H4 | 丙炔-3-基 |
No. | R3 | R4 | R5 |
1659 | CH3 | 4-OH-C6H4 | 3-甲基-丁-2-烯-1-基 |
1660 | CH3 | 2-OCH3-C6H4 | H |
1661 | CH3 | 2-OCH3-C6H4 | CH3 |
1662 | CH3 | 2-OCH3-C6H4 | C2H5 |
1663 | CH3 | 2-OCH3-C6H4 | n-C3H7 |
1664 | CH3 | 2-OCH3-C6H4 | i-C3H7 |
1665 | CH3 | 2-OCH3-C6H4 | n-C4H9 |
1666 | CH3 | 2-OCH3-C6H4 | t-C4H9 |
1667 | CH3 | 2-OCH3-C6H4 | n-C6H13 |
1668 | CH3 | 2-OCH3-C6H4 | 丙-1-烯-3-基 |
1669 | CH3 | 2-OCH3-C6H4 | (E)-1-氯丙-1-烯-3-基 |
1670 | CH3 | 2-OCH3-C6H4 | 丙炔-3-基 |
1671 | CH3 | 2-OCH3-C6H4 | 3-甲基-丁-2-烯-1-基 |
1672 | CH3 | 3-OCH3-C6H4 | H |
1673 | CH3 | 3-OCH3-C6H4 | CH3 |
1674 | CH3 | 3-OCH3-C6H4 | C2H5 |
1675 | CH3 | 3-OCH3-C6H4 | n-C3H7 |
1676 | CH3 | 3-OCH3-C6H4 | i-C3H7 |
1677 | CH3 | 3-OCH3-C6H4 | n-C4H9 |
1678 | CH3 | 3-OCH3-C6H4 | t-C4H9 |
No. | R3 | R4 | R5 |
1679 | CH3 | 3-OCH3-C6H4 | n-C6H13 |
1680 | CH3 | 3-OCH3-C6H4 | 丙-1-烯-3-基 |
1681 | CH3 | 3-OCH3-C6H4 | (E)-1-氯丙-1-烯-3-基 |
1682 | CH3 | 3-OCH3-C6H4 | 丙炔-3-基 |
1683 | CH3 | 3-OCH3-C6H4 | 3-甲基-丁-2-烯-1-基 |
1684 | CH3 | 4-OCH3-C6H4 | H |
1685 | CH3 | 4-OCH3-C6H4 | CH3 |
1686 | CH3 | 4-OCH3-C6H4 | C2H5 |
1687 | CH3 | 4-OCH3-C6H4 | n-C3H7 |
1688 | CH3 | 4-OCH3-C6H4 | i-C3H7 |
1689 | CH3 | 4-OCH3-C6H4 | n-C4H9 |
1690 | CH3 | 4-OCH3-C6H4 | t-C4H9 |
1691 | CH3 | 4-OCH3-C6H4 | n-C6H13 |
1692 | CH3 | 4-OCH3-C6H4 | 丙-1-烯-3-基 |
1693 | CH3 | 4-OCH3-C6H4 | (E)-1-氯丙-1-烯-3-基 |
1694 | CH3 | 4-OCH3-C6H4 | 丙炔-3-基 |
1695 | CH3 | 4-OCH3-C6H4 | 3-甲基-丁-2-烯-1-基 |
1696 | CH3 | 2-OC2H5-C6H4 | H |
1697 | CH3 | 2-OC2H5-C6H4 | CH3 |
1698 | CH3 | 2-OC2H5-C6H4 | C2H5 |
No. | R3 | R4 | R5 |
1699 | CH3 | 2-OC2H5-C6H4 | n-C3H7 |
1700 | CH3 | 2-OC2H5-C6H4 | i-C3H7 |
1701 | CH3 | 2-OC2H5-C6H4 | n-C4H9 |
1702 | CH3 | 2-OC2H5-C6H4 | t-C4H9 |
1703 | CH3 | 2-OC2H5-C6H4 | n-C6H13 |
1704 | CH3 | 2-OC2H5-C6H4 | 丙-1-烯-3-基 |
1705 | CH3 | 2-OC2H5-C6H4 | (E)-1-氯丙-1-烯-3-基 |
1706 | CH3 | 2-OC2H5-C6H4 | 丙炔-3-基 |
1707 | CH3 | 2-OC2H5-C6H4 | 3-甲基-丁-2-烯-1-基 |
1708 | CH3 | 3-OC2H5-C6H4 | H |
1709 | CH3 | 3-OC2H5-C6H4 | CH3 |
1710 | CH3 | 3-OC2H5-C6H4 | C2H5 |
1711 | CH3 | 3-OC2H5-C6H4 | n-C3H7 |
1712 | CH3 | 3-OC2H5-C6H4 | i-C3H7 |
1713 | CH3 | 3-OC2H5-C6H4 | n-C4H9 |
1714 | CH3 | 3-OC2H5-C6H4 | t-C4H9 |
1715 | CH3 | 3-OC2H5-C6H4 | n-C6H13 |
1716 | CH3 | 3-OC2H5-C6H4 | 丙-1-烯-3-基 |
1717 | CH3 | 3-OC2H5-C6H4 | (E)-1-氯丙-1-烯-3-基 |
1718 | CH3 | 3-OC2H5-C6H4 | 丙炔-3-基 |
No. | R3 | R4 | R5 |
1719 | CH3 | 3-OC2H5-C6H4 | 3-甲基-丁-2-烯-1-基 |
1720 | CH3 | 4-OC2H5-C6H4 | H |
1721 | CH3 | 4-OC2H5-C6H4 | CH3 |
1722 | CH3 | 4-OC2H5-C6H4 | C2H5 |
1723 | CH3 | 4-OC2H5-C6H4 | n-C3H7 |
1724 | CH3 | 4-OC2H5-C6H4 | i-C3H7 |
1725 | CH3 | 4-OC2H5-C6H4 | n-C4H9 |
1726 | CH3 | 4-OC2H5-C6H4 | t-C4H9 |
1727 | CH3 | 4-OC2H5-C6H4 | n-C6H13 |
1728 | CH3 | 4-OC2H5-C6H4 | 丙-1-烯-3-基 |
1729 | CH3 | 4-OC2H5-C6H4 | (E)-1-氯丙-1-烯-3-基 |
1730 | CH3 | 4-OC2H5-C6H4 | 丙炔-3-基 |
1731 | CH3 | 4-OC2H5-C6H4 | 3-甲基-丁-2-烯-1-基 |
1732 | CH3 | 2-O-(i-C3H7)-C6H4 | H |
1733 | CH3 | 2-O-(i-C3H7)-C6H4 | CH3 |
1734 | CH3 | 2-O-(i-C3H7)-C6H4 | C2H5 |
1735 | CH3 | 2-O-(i-C3H7)-C6H4 | n-C3H7 |
1736 | CH3 | 2-O-(i-C3H7)-C6H4 | i-C3H7 |
1737 | CH3 | 2-O-(i-C3H7)-C6H4 | n-C4H9 |
1738 | CH3 | 2-O-(i-C3H7)-C6H4 | t-C4H9 |
No. | R3 | R4 | R5 |
1739 | CH3 | 2-O-(i-C3H7)-C6H4 | n-C6H13 |
1740 | CH3 | 2-O-(i-C3H7)-C6H4 | 丙-1-烯-3-基 |
1741 | CH3 | 2-O-(i-C3H7)-C6H4 | (E)-1-氯丙-1-烯-3-基 |
1742 | CH3 | 2-O-(i-C3H7)-C6H4 | 丙炔-3-基 |
1743 | CH3 | 2-O-(i-C3H7)-C6H4 | 3-甲基-丁-2-烯-1-基 |
1744 | CH3 | 3-O-(i-C3H7)-C6H4 | H |
1745 | CH3 | 3-O-(i-C3H7)-C6H4 | CH3 |
1746 | CH3 | 3-O-(i-C3H7)-C6H4 | C2H5 |
1747 | CH3 | 3-O-(i-C3H7)-C6H4 | n-C3H7 |
1748 | CH3 | 3-O-(i-C3H7)-C6H4 | i-C3H7 |
1749 | CH3 | 3-O-(i-C3H7)-C6H4 | n-C4H9 |
1750 | CH3 | 3-O-(i-C3H7)-C6H4 | t-C4H9 |
1751 | CH3 | 3-O-(i-C3H7)-C6H4 | n-C6H13 |
1752 | CH3 | 3-O-(i-C3H7)-C6H4 | 丙-1-烯-3-基 |
1753 | CH3 | 3-O-(i-C3H7)-C6H4 | (E)-1-氯丙-1-烯-3-基 |
1754 | CH3 | 3-O-(i-C3H7)-C6H4 | 丙炔-3-基 |
1755 | CH3 | 3-O-(i-C3H7)-C6H4 | 3-甲基-丁-2-烯-1-基 |
1756 | CH3 | 4-O-(i-C3H7)-C6H4 | H |
1757 | CH3 | 4-O-(i-C3H7)-C6H4 | CH3 |
1758 | CH3 | 4-O-(i-C3H7)-C6H4 | C2H5 |
No. | R3 | R4 | R5 |
1759 | CH3 | 4-O-(i-C3H7)-C6H4 | n-C3H7 |
1760 | CH3 | 4-O-(i-C3H7)-C6H4 | i-C3H7 |
1761 | CH3 | 4-O-(i-C3H7)-C6H4 | n-C4H9 |
1762 | CH3 | 4-O-(i-C3H7)-C6H4 | t-C4H9 |
1763 | CH3 | 4-O-(i-C3H7)-C6H4 | n-C6H13 |
1764 | CH3 | 4-O-(i-C3H7)-C6H4 | 丙-1-烯-3-基 |
1765 | CH3 | 4-O-(i-C3H7)-C6H4 | (E)-1-氯丙-1-烯-3-基 |
1766 | CH3 | 4-O-(i-C3H7)-C6H4 | 丙炔-3-基 |
1767 | CH3 | 4-O-(i-C3H7)-C6H4 | 3-甲基-丁-2-烯-1-基 |
1768 | CH3 | 2-O-(t-C4H9)-C6H4 | H |
1769 | CH3 | 2-O-(t-C4H9)-C6H4 | CH3 |
1770 | CH3 | 2-O-(t-C4H9)-C6H4 | C2H5 |
1771 | CH3 | 2-O-(t-C4H9)-C6H4 | n-C3H7 |
1772 | CH3 | 2-O-(t-C4H9)-C6H4 | i-C3H7 |
1773 | CH3 | 2-O-(t-C4H9)-C6H4 | n-C4H9 |
1774 | CH3 | 2-O-(t-C4H9)-C6H4 | t-C4H9 |
1775 | CH3 | 2-O-(t-C4H9)-C6H4 | n-C6H13 |
1776 | CH3 | 2-O-(t-C4H9)-C6H4 | 丙-1-烯-3-基 |
1777 | CH3 | 2-O-(t-C4H9)-C6H4 | (E)-1-氯丙-1-烯-3-基 |
1778 | CH3 | 2-O-(t-C4H9)-C6H4 | 丙炔-3-基 |
No. | R3 | R4 | R5 |
1779 | CH3 | 2-O-(t-C4H9)-C6H4 | 3-甲基-丁-2-烯-1-基 |
1780 | CH3 | 3-O-(t-C4H9)-C6H4 | H |
1781 | CH3 | 3-O-(t-C4H9)-C6H4 | CH3 |
1782 | CH3 | 3-O-(t-C4H9)-C6H4 | C2H5 |
1783 | CH3 | 3-O-(t-C4H9)-C6H4 | n-C3H7 |
1784 | CH3 | 3-O-(t-C4H9)-C6H4 | i-C3H7 |
1785 | CH3 | 3-O-(t-C4H9)-C6H4 | n-C4H9 |
1786 | CH3 | 3-O-(t-C4H9)-C6H4 | t-C4H9 |
1787 | CH3 | 3-O-(t-C4H9)-C6H4 | n-C6H13 |
1788 | CH3 | 3-O-(t-C4H9)-C6H4 | 丙-1-烯-3-基 |
1789 | CH3 | 3-O-(t-C4H9)-C6H4 | (E)-1-氯丙-1-烯-3-基 |
1790 | CH3 | 3-O-(t-C4H9)-C6H4 | 丙炔-3-基 |
1791 | CH3 | 3-O-(t-C4H9)-C6H4 | 3-甲基-丁-2-烯-1-基 |
1792 | CH3 | 4-O-(t-C4H9)-C6H4 | H |
1793 | CH3 | 4-O-(t-C4H9)-C6H4 | CH3 |
1794 | CH3 | 4-O-(t-C4H9)-C6H4 | C2H5 |
1795 | CH3 | 4-O-(t-C4H9)-C6H4 | n-C3H7 |
1796 | CH3 | 4-O-(t-C4H9)-C6H4 | i-C3H7 |
1797 | CH3 | 4-O-(t-C4H9)-C6H4 | n-C4H9 |
1798 | CH3 | 4-O-(t-C4H9)-C6H4 | t-C4H9 |
No. | R3 | R4 | R5 |
1799 | CH3 | 4-O-(t-C4H9)-C6H4 | n-C6H13 |
1800 | CH3 | 4-O-(t-C4H9)-C6H4 | 丙-1-烯-3-基 |
1801 | CH3 | 4-O-(t-C4H9)-C6H4 | (E)-1-氯丙-1-烯-3-基 |
1802 | CH3 | 4-O-(t-C4H9)-C6H4 | 丙炔-3-基 |
1803 | CH3 | 4-O-(t-C4H9)-C6H4 | 3-甲基-丁-2-烯-1-基 |
1804 | CH3 | 2-CF3-C6H4 | H |
1805 | CH3 | 2-CF3-C6H4 | CH3 |
1806 | CH3 | 2-CF3-C6H4 | C2H5 |
1807 | CH3 | 2-CF3-C6H4 | n-C3H7 |
1808 | CH3 | 2-CF3-C6H4 | i-C3H7 |
1809 | CH3 | 2-CF3-C6H4 | n-C4H9 |
1810 | CH3 | 2-CF3-C6H4 | t-C4H9 |
1811 | CH3 | 2-CF3-C6H4 | n-C6H13 |
1812 | CH3 | 2-CF3-C6H4 | 丙-1-烯-3-基 |
1813 | CH3 | 2-CF3-C6H4 | (E)-1-氯丙-1-烯-3-基 |
1814 | CH3 | 2-CF3-C6H4 | 丙炔-3-基 |
1815 | CH3 | 2-CF3-C6H4 | 3-甲基-丁-2-烯-1-基 |
1816 | CH3 | 3-CF3-C6H4 | H |
1817 | CH3 | 3-CF3-C6H4 | CH3 |
1818 | CH3 | 3-CF3-C6H4 | C2H5 |
No. | R3 | R4 | R5 |
1819 | CH3 | 3-CF3-C6H4 | n-C3H7 |
1820 | CH3 | 3-CF3-C6H4 | i-C3H7 |
1821 | CH3 | 3-CF3-C6H4 | n-C4H9 |
1822 | CH3 | 3-CF3-C6H4 | t-C4H9 |
1823 | CH3 | 3-CF3-C6H4 | n-C6H13 |
1824 | CH3 | 3-CF3-C6H4 | 丙-1-烯-3-基 |
1825 | CH3 | 3-CF3-C6H4 | (E)-1-氯丙-1-烯-3-基 |
1826 | CH3 | 3-CF3-C6H4 | 丙炔-3-基 |
1827 | CH3 | 3-CF3-C6H4 | 3-甲基-丁-2-烯-1-基 |
1828 | CH3 | 4-CF3-C6H4 | H |
1829 | CH3 | 4-CF3-C6H4 | CH3 |
1830 | CH3 | 4-CF3-C6H4 | C2H5 |
1831 | CH3 | 4-CF3-C6H4 | n-C3H7 |
1832 | CH3 | 4-CF3-C6H4 | i-C3H7 |
1833 | CH3 | 4-CF3-C6H4 | n-C4H9 |
1834 | CH3 | 4-CF3-C6H4 | t-C4H9 |
1835 | CH3 | 4-CF3-C6H4 | n-C6H13 |
1836 | CH3 | 4-CF3-C6H4 | 丙-1-烯-3-基 |
1837 | CH3 | 4-CF3-C6H4 | (E)-1-氯丙-1-烯-3-基 |
1838 | CH3 | 4-CF3-C6H4 | 丙炔-3-基 |
No. | R3 | R4 | R5 |
1839 | CH3 | 4-CF3-C6H4 | 3-甲基-丁-2-烯-1-基 |
1840 | CH3 | 2-NH2-C6H4 | H |
1841 | CH3 | 2-NH2-C6H4 | CH3 |
1842 | CH3 | 2-NH2-C6H4 | C2H5 |
1843 | CH3 | 2-NH2-C6H4 | n-C3H7 |
1844 | CH3 | 2-NH2-C6H4 | i-C3H7 |
1845 | CH3 | 2-NH2-C6H4 | n-C4H9 |
1846 | CH3 | 2-NH2-C6H4 | t-C4H9 |
1847 | CH3 | 2-NH2-C6H4 | n-C6H13 |
1848 | CH3 | 2-NH2-C6H4 | 丙-1-烯-3-基 |
1849 | CH3 | 2-NH2-C6H4 | (E)-1-氯丙-1-烯-3-基 |
1850 | CH3 | 2-NH2-C6H4 | 丙炔-3-基 |
1851 | CH3 | 2-NH2-C6H4 | 3-甲基-丁-2-烯-1-基 |
1852 | CH3 | 3-NH2-C6H4 | H |
1853 | CH3 | 3-NH2-C6H4 | CH3 |
1854 | CH3 | 3-NH2-C6H4 | C2H5 |
1855 | CH3 | 3-NH2-C6H4 | n-C3H7 |
1856 | CH3 | 3-NH2-C6H4 | i-C3H7 |
1857 | CH3 | 3-NH2-C6H4 | n-C4H9 |
1858 | CH3 | 3-NH2-C6H4 | t-C4H9 |
No. | R3 | R4 | R5 |
1859 | CH3 | 3-NH2-C6H4 | n-C6H13 |
1860 | CH3 | 3-NH2-C6H4 | 丙-1-烯-3-基 |
1861 | CH3 | 3-NH2-C6H4 | (E)-1-氯丙-1-烯-3-基 |
1862 | CH3 | 3-NH2-C6H4 | 丙炔-3-基 |
1863 | CH3 | 3-NH2-C6H4 | 3-甲基-丁-2-烯-1-基 |
1864 | CH3 | 4-NH2-C6H4 | H |
1865 | CH3 | 4-NH2-C6H4 | CH3 |
1866 | CH3 | 4-NH2-C6H4 | C2H5 |
1867 | CH3 | 4-NH2-C6H4 | n-C3H7 |
1868 | CH3 | 4-NH2-C6H4 | i-C3H7 |
1869 | CH3 | 4-NH2-C6H4 | n-C4H9 |
1870 | CH3 | 4-NH2-C6H4 | t-C4H9 |
1871 | CH3 | 4-NH2-C6H4 | n-C6H13 |
1872 | CH3 | 4-NH2-C6H4 | 丙-1-烯-3-基 |
1873 | CH3 | 4-NH2-C6H4 | (E)-1-氯丙-1-烯-3-基 |
1874 | CH3 | 4-NH2-C6H4 | 丙炔-3-基 |
1875 | CH3 | 4-NH2-C6H4 | 3-甲基-丁-2-烯-1-基 |
1876 | CH3 | 2-NMe2-C6H4 | H |
1877 | CH3 | 2-NMe2-C6H4 | CH3 |
1878 | CH3 | 2-NMe2-C6H4 | C2H5 |
No. | R3 | R4 | R5 |
1879 | CH3 | 2-NMe2-C6H4 | n-C3H7 |
1880 | CH3 | 2-NMe2-C6H4 | i-C3H7 |
1881 | CH3 | 2-NMe2-C6H4 | n-C4H9 |
1882 | CH3 | 2-NMe2-C6H4 | t-C4H9 |
1883 | CH3 | 2-NMe2-C6H4 | n-C6H13 |
1884 | CH3 | 2-NMe2-C6H4 | 丙-1-烯-3-基 |
1885 | CH3 | 2-NMe2-C6H4 | (E)-1-氯丙-1-烯-3-基 |
1886 | CH3 | 2-NMe2-C6H4 | 丙炔-3-基 |
1887 | CH3 | 2-NMe2-C6H4 | 3-甲基-丁-2-烯-1-基 |
1888 | CH3 | 3-NMe2-C6H4 | H |
1889 | CH3 | 3-NMe2-C6H4 | CH3 |
1890 | CH3 | 3-NMe2-C6H4 | C2H5 |
1891 | CH3 | 3-NMe2-C6H4 | n-C3H7 |
1892 | CH3 | 3-NMe2-C6H4 | i-C3H7 |
1893 | CH3 | 3-NMe2-C6H4 | n-C4H9 |
1894 | CH3 | 3-NMe2-C6H4 | t-C4H9 |
1895 | CH3 | 3-NMe2-C6H4 | n-C6H13 |
1896 | CH3 | 3-NMe2-C6H4 | 丙-1-烯-3-基 |
1897 | CH3 | 3-NMe2-C6H4 | (E)-1-氯丙-1-烯-3-基 |
1898 | CH3 | 3-NMe2-C6H4 | 丙炔-3-基 |
No. | R3 | R4 | R5 |
1899 | CH3 | 3-NMe2-C6H4 | 3-甲基-丁-2-烯-1-基 |
1900 | CH3 | 4-NMe2-C6H4 | H |
1901 | CH3 | 4-NMe2-C6H4 | CH3 |
1902 | CH3 | 4-NMe2-C6H4 | C2H5 |
1903 | CH3 | 4-NMe2-C6H4 | n-C3H7 |
1904 | CH3 | 4-NMe2-C6H4 | i-C3H7 |
1905 | CH3 | 4-NMe2-C6H4 | n-C4H9 |
1906 | CH3 | 4-NMe2-C6H4 | t-C4H9 |
1907 | CH3 | 4-NMe2-C6H4 | n-C6H13 |
1908 | CH3 | 4-NMe2-C6H4 | 丙-1-烯-3-基 |
1909 | CH3 | 4-NMe2-C6H4 | (E)-1-氯丙-1-烯-3-基 |
1910 | CH3 | 4-NMe2-C6H4 | 丙炔-3-基 |
1911 | CH3 | 4-NMe2-C6H4 | 3-甲基-丁-2-烯-1-基 |
1912 | CH3 | 2-氨基硫代羰基 -C6H4 | H |
1913 | CH3 | 2-氨基硫代羰基 -C6H4 | CH3 |
1914 | CH3 | 2-氨基硫代羰基 -C6H4 | C2H5 |
1915 | CH3 | 2-氨基硫代羰基 -C6H4 | n-C3H7 |
1916 | CH3 | 2-氨基硫代羰基 -C6H4 | i-C3H7 |
1917 | CH3 | 2-氨基硫代羰基 -C6H4 | n-C4H9 |
1918 | CH3 | 2-氨基硫代羰基 -C6H4 | t-C4H9 |
No. | R3 | R4 | R5 |
1919 | CH3 | 2-氨基硫代羰基 -C6H4 | n-C6H13 |
1920 | CH3 | 2-氨基硫代羰基 -C6H4 | 丙-1-烯-3-基 |
1921 | CH3 | 2-氨基硫代羰基 -C6H4 | (E)-1-氯丙-1-烯-3-基 |
1922 | CH3 | 2-氨基硫代羰基 -C6H4 | 丙炔-3-基 |
1923 | CH3 | 2-氨基硫代羰基 -C6H4 | 3-甲基-丁-2-烯-1-基 |
1924 | CH3 | 3-氨基硫代羰基 -C6H4 | H |
1925 | CH3 | 3-氨基硫代羰基 -C6H4 | CH3 |
1926 | CH3 | 3-氨基硫代羰基 -C6H4 | C2H5 |
1927 | CH3 | 3-氨基硫代羰基 -C6H4 | n-C3H7 |
1928 | CH3 | 3-氨基硫代羰基 -C6H4 | i-C3H7 |
1929 | CH3 | 3-氨基硫代羰基 -C6H4 | n-C4H9 |
1930 | CH3 | 3-氨基硫代羰基 -C6H4 | t-C4H9 |
1931 | CH3 | 3-氨基硫代羰基 -C6H4 | n-C6H13 |
1932 | CH3 | 3-氨基硫代羰基 -C6H4 | 丙-1-烯-3-基 |
1933 | CH3 | 3-氨基硫代羰基 -C6H4 | (E)-1-氯丙-1-烯-3-基 |
1934 | CH3 | 3-氨基硫代羰基 -C6H4 | 丙炔-3-基 |
1935 | CH3 | 3-氨基硫代羰基 -C6H4 | 3-甲基-丁-2-烯-1-基 |
1936 | CH3 | 4-氨基硫代羰基 -C6H4 | H |
1937 | CH3 | 4-氨基硫代羰基 -C6H4 | CH3 |
1938 | CH3 | 4-氨基硫代羰基 -C6H4 | C2H5 |
No. | R3 | R4 | R5 |
1939 | CH3 | 4-氨基硫代羰基 -C6H4 | n-C3H7 |
1940 | CH3 | 4-氨基硫代羰基 -C6H4 | i-C3H7 |
1941 | CH3 | 4-氨基硫代羰基 -C6H4 | n-C4H9 |
1942 | CH3 | 4-氨基硫代羰基 -C6H4 | t-C4H9 |
1943 | CH3 | 4-氨基硫代羰基 -C6H4 | n-C6H13 |
1944 | CH3 | 4-氨基硫代羰基 -C6H4 | 丙-1-烯-3-基 |
1945 | CH3 | 4-氨基硫代羰基 -C6H4 | (E)-1-氯丙-1-烯-3-基 |
1946 | CH3 | 4-氨基硫代羰基 -C6H4 | 丙炔-3-基 |
1947 | CH3 | 4-氨基硫代羰基 -C6H4 | 3-甲基-丁-2-烯-1-基 |
1948 | CH3 | 2-OCF3-C6H4 | H |
1949 | CH3 | 2-OCF3-C6H4 | CH3 |
1950 | CH3 | 2-OCF3-C6H4 | C2H5 |
1951 | CH3 | 2-OCF3-C6H4 | n-C3H7 |
1952 | CH3 | 2-OCF3-C6H4 | i-C3H7 |
1953 | CH3 | 2-OCF3-C6H4 | n-C4H9 |
1954 | CH3 | 2-OCF3-C6H4 | t-C4H9 |
1955 | CH3 | 2-OCF3-C6H4 | n-C6H13 |
1956 | CH3 | 2-OCF3-C6H4 | 丙-1-烯-3-基 |
1957 | CH3 | 2-OCF3-C6H4 | (E)-1-氯丙-1-烯-3-基 |
1958 | CH3 | 2-OCF3-C6H4 | 丙炔-3-基 |
No. | R3 | R4 | R5 |
1959 | CH3 | 2-OCF3-C6H4 | 3-甲基-丁-2-烯-1-基 |
1960 | CH3 | 3-OCF3-C6H4 | H |
1961 | CH3 | 3-OCF3-C6H4 | CH3 |
1962 | CH3 | 3-OCF3-C6H4 | C2H5 |
1963 | CH3 | 3-OCF3-C6H4 | n-C3H7 |
1964 | CH3 | 3-OCF3-C6H4 | i-C3H7 |
1965 | CH3 | 3-OCF3-C6H4 | n-C4H9 |
1966 | CH3 | 3-OCF3-C6H4 | t-C4H9 |
1967 | CH3 | 3-OCF3-C6H4 | n-C6H13 |
1968 | CH3 | 3-OCF3-C6H4 | 丙-1-烯-3-基 |
1969 | CH3 | 3-OCF3-C6H4 | (E)-1-氯丙-1-烯-3-基 |
1970 | CH3 | 3-OCF3-C6H4 | 丙炔-3-基 |
1971 | CH3 | 3-OCF3-C6H4 | 3-甲基-丁-2-烯-1-基 |
1972 | CH3 | 4-OCF3-C6H4 | H |
1973 | CH3 | 4-OCF3-C6H4 | CH3 |
1974 | CH3 | 4-OCF3-C6H4 | C2H5 |
1975 | CH3 | 4-OCF3-C6H4 | n-C3H7 |
1976 | CH3 | 4-OCF3-C6H4 | i-C3H7 |
1977 | CH3 | 4-OCF3-C6H4 | n-C4H9 |
1978 | CH3 | 4-OCF3-C6H4 | t-C4H9 |
No. | R3 | R4 | R5 |
1979 | CH3 | 4-OCF3-C6H4 | n-C6H13 |
1980 | CH3 | 4-OCF3-C6H4 | 丙-1-烯-3-基 |
1981 | CH3 | 4-OCF3-C6H4 | (E)-1-氯丙-1-烯-3-基 |
1982 | CH3 | 4-OCF3-C6H4 | 丙炔-3-基 |
1983 | CH3 | 4-OCF3-C6H4 | 3-甲基-丁-2-烯-1-基 |
1984 | CH3 | 2-SCH3-C6H4 | H |
1985 | CH3 | 2-SCH3-C6H4 | CH3 |
1986 | CH3 | 2-SCH3-C6H4 | C2H5 |
1987 | CH3 | 2-SCH3-C6H4 | n-C3H7 |
1988 | CH3 | 2-SCH3-C6H4 | i-C3H7 |
1989 | CH3 | 2-SCH3-C6H4 | n-C4H9 |
1990 | CH3 | 2-SCH3-C6H4 | t-C4H9 |
1991 | CH3 | 2-SCH3-C6H4 | n-C6H13 |
1992 | CH3 | 2-SCH3-C6H4 | 丙-1-烯-3-基 |
1993 | CH3 | 2-SCH3-C6H4 | (E)-1-氯丙-1-烯-3-基 |
1994 | CH3 | 2-SCH3-C6H4 | 丙炔-3-基 |
1995 | CH3 | 2-SCH3-C6H4 | 3-甲基-丁-2-烯-1-基 |
1996 | CH3 | 3-SCH3-C6H4 | H |
1997 | CH3 | 3-SCH3-C6H4 | CH3 |
1998 | CH3 | 3-SCH3-C6H4 | C2H5 |
No. | R3 | R4 | R5 |
1999 | CH3 | 3-SCH3-C6H4 | n-C3H7 |
2000 | CH3 | 3-SCH3-C6H4 | i-C3H7 |
2001 | CH3 | 3-SCH3-C6H4 | n-C4H9 |
2002 | CH3 | 3-SCH3-C6H4 | t-C4H9 |
2003 | CH3 | 3-SCH3-C6H4 | n-C6H13 |
2004 | CH3 | 3-SCH3-C6H4 | 丙-1-烯-3-基 |
2005 | CH3 | 3-SCH3-C6H4 | (E)-1-氯丙-1-烯-3-基 |
2006 | CH3 | 3-SCH3-C6H4 | 丙炔-3-基 |
2007 | CH3 | 3-SCH3-C6H4 | 3-甲基-丁-2-烯-1-基 |
2008 | CH3 | 4-SCH3-C6H4 | H |
2009 | CH3 | 4-SCH3-C6H4 | CH3 |
2010 | CH3 | 4-SCH3-C6H4 | C2H5 |
2011 | CH3 | 4-SCH3-C6H4 | n-C3H7 |
2012 | CH3 | 4-SCH3-C6H4 | i-C3H7 |
2013 | CH3 | 4-SCH3-C6H4 | n-C4H9 |
2014 | CH3 | 4-SCH3-C6H4 | t-C4H9 |
2015 | CH3 | 4-SCH3-C6H4 | n-C6H13 |
2016 | CH3 | 4-SCH3-C6H4 | 丙-1-烯-3-基 |
2017 | CH3 | 4-SCH3-C6H4 | (E)-1-氯丙-1-烯-3-基 |
2018 | CH3 | 4-SCH3-C6H4 | 丙炔-3-基 |
No. | R3 | R4 | R5 |
2019 | CH3 | 4-SCH3-C6H4 | 3-甲基-丁-2-烯-1-基 |
2020 | CH3 | 2-甲基磺酰基 -C6H4 | H |
2021 | CH3 | 2-甲基磺酰基 -C6H4 | CH3 |
2022 | CH3 | 2-甲基磺酰基 -C6H4 | C2H5 |
2023 | CH3 | 2-甲基磺酰基 -C6H4 | n-C3H7 |
2024 | CH3 | 2-甲基磺酰基 -C6H4 | i-C3H7 |
2025 | CH3 | 2-甲基磺酰基 -C6H4 | n-C4H9 |
2026 | CH3 | 2-甲基磺酰基 -C6H4 | t-C4H9 |
2027 | CH3 | 2-甲基磺酰基 -C6H4 | n-C6H13 |
2028 | CH3 | 2-甲基磺酰基 -C6H4 | 丙-1-烯-3-基 |
2029 | CH3 | 2-甲基磺酰基 -C6H4 | (E)-1-氯丙-1-烯-3-基 |
2030 | CH3 | 2-甲基磺酰基 -C6H4 | 丙炔-3-基 |
2031 | CH3 | 2-甲基磺酰基 -C6H4 | 3-甲基-丁-2-烯-1-基 |
2032 | CH3 | 3-甲基磺酰基 -C6H4 | H |
2033 | CH3 | 3-甲基磺酰基 -C6H4 | CH3 |
2034 | CH3 | 3-甲基磺酰基 -C6H4 | C2H5 |
2035 | CH3 | 3-甲基磺酰基 -C6H4 | n-C3H7 |
2036 | CH3 | 3-甲基磺酰基 -C6H4 | i-C3H7 |
2037 | CH3 | 3-甲基磺酰基 -C6H4 | n-C4H9 |
2038 | CH3 | 3-甲基磺酰基 -C6H4 | t-C4H9 |
No. | R3 | R4 | R5 |
2039 | CH3 | 3-甲基磺酰基 -C6H4 | n-C6H13 |
2040 | CH3 | 3-甲基磺酰基 -C6H4 | 丙-1-烯-3-基 |
2041 | CH3 | 3-甲基磺酰基 -C6H4 | (E)-1-氯丙-1-烯-3-基 |
2042 | CH3 | 3-甲基磺酰基 -C6H4 | 丙炔-3-基 |
2043 | CH3 | 3-甲基磺酰基 -C6H4 | 3-甲基-丁-2-烯-1-基 |
2044 | CH3 | 4-甲基磺酰基 -C6H4 | H |
2045 | CH3 | 4-甲基磺酰基 -C6H4 | CH3 |
2046 | CH3 | 4-甲基磺酰基 -C6H4 | C2H5 |
2047 | CH3 | 4-甲基磺酰基 -C6H4 | n-C3H7 |
2048 | CH3 | 4-甲基磺酰基 -C6H4 | i-C3H7 |
2049 | CH3 | 4-甲基磺酰基 -C6H4 | n-C4H9 |
2050 | CH3 | 4-甲基磺酰基 -C6H4 | t-C4H9 |
2051 | CH3 | 4-甲基磺酰基 -C6H4 | n-C6H13 |
2052 | CH3 | 4-甲基磺酰基 -C6H4 | 丙-1-烯-3-基 |
2053 | CH3 | 4-甲基磺酰基 -C6H4 | (E)-1-氯丙-1-烯-3-基 |
2054 | CH3 | 4-甲基磺酰基 -C6H4 | 丙炔-3-基 |
2055 | CH3 | 4-甲基磺酰基 -C6H4 | 3-甲基-丁-2-烯-1-基 |
2056 | CH3 | 2-甲氧羰基 -C6H4 | H |
2057 | CH3 | 2-甲氧羰基 -C6H4 | CH3 |
2058 | CH3 | 2-甲氧羰基 -C6H4 | C2H5 |
No. | R3 | R4 | R5 |
2059 | CH3 | 2-甲氧羰基 -C6H4 | n-C3H7 |
2060 | CH3 | 2-甲氧羰基 -C6H4 | i-C3H7 |
2061 | CH3 | 2-甲氧羰基 -C6H4 | n-C4H9 |
2062 | CH3 | 2-甲氧羰基 -C6H4 | t-C4H9 |
2063 | CH3 | 2-甲氧羰基 -C6H4 | n-C6H13 |
2064 | CH3 | 2-甲氧羰基 -C6H4 | 丙-1-烯-3-基 |
2065 | CH3 | 2-甲氧羰基 -C6H4 | (E)-1-氯丙-1-烯-3-基 |
2066 | CH3 | 2-甲氧羰基 -C6H4 | 丙炔-3-基 |
2067 | CH3 | 2-甲氧羰基 -C6H4 | 3-甲基-丁-2-烯-1-基 |
2068 | CH3 | 3-甲氧羰基 -C6H4 | H |
2069 | CH3 | 3-甲氧羰基 -C6H4 | CH3 |
2070 | CH3 | 3-甲氧羰基 -C6H4 | C2H5 |
2071 | CH3 | 3-甲氧羰基 -C6H4 | n-C3H7 |
2072 | CH3 | 3-甲氧羰基 -C6H4 | i-C3H7 |
2073 | CH3 | 3-甲氧羰基 -C6H4 | n-C4H9 |
2074 | CH3 | 3-甲氧羰基 -C6H4 | t-C4H9 |
2075 | CH3 | 3-甲氧羰基 -C6H4 | n-C6H13 |
2076 | CH3 | 3-甲氧羰基 -C6H4 | 丙-1-烯-3-基 |
2077 | CH3 | 3-甲氧羰基 -C6H4 | (E)-1-氯丙-1-烯-3-基 |
2078 | CH3 | 3-甲氧羰基 -C6H4 | 丙炔-3-基 |
No. | R3 | R4 | R5 |
2079 | CH3 | 3-甲氧羰基 -C6H4 | 3-甲基-丁-2-烯-1-基 |
2080 | CH3 | 4-甲氧羰基 -C6H4 | H |
2081 | CH3 | 4-甲氧羰基 -C6H4 | CH3 |
2082 | CH3 | 4-甲氧羰基 -C6H4 | C2H5 |
2083 | CH3 | 4-甲氧羰基 -C6H4 | n-C3H7 |
2084 | CH3 | 4-甲氧羰基 -C6H4 | i-C3H7 |
2085 | CH3 | 4-甲氧羰基 -C6H4 | n-C4H9 |
2086 | CH3 | 4-甲氧羰基 -C6H4 | t-C4H9 |
2087 | CH3 | 4-甲氧羰基 -C6H4 | n-C6H13 |
2088 | CH3 | 4-甲氧羰基 -C6H4 | 丙-1-烯-3-基 |
2089 | CH3 | 4-甲氧羰基 -C6H4 | (E)-1-氯丙-1-烯-3-基 |
2090 | CH3 | 4-甲氧羰基 -C6H4 | 丙炔-3-基 |
2091 | CH3 | 4-甲氧羰基 -C6H4 | 3-甲基-丁-2-烯-1-基 |
2092 | CH3 | 2-乙氧羰基 -C6H4 | H |
2093 | CH3 | 2-乙氧羰基 -C6H4 | CH3 |
2094 | CH3 | 2-乙氧羰基 -C6H4 | C2H5 |
2095 | CH3 | 2-乙氧羰基 -C6H4 | n-C3H7 |
2096 | CH3 | 2-乙氧羰基 -C6H4 | i-C3H7 |
2097 | CH3 | 2-乙氧羰基 -C6H4 | n-C4H9 |
2098 | CH3 | 2-乙氧羰基 -C6H4 | t-C4H9 |
No. | R3 | R4 | R5 |
2099 | CH3 | 2-乙氧羰基 -C6H4 | n-C6H13 |
2100 | CH3 | 2-乙氧羰基 -C6H4 | 丙-1-烯-3-基 |
2101 | CH3 | 2-乙氧羰基 -C6H4 | (E)-1-氯丙-1-烯-3-基 |
2102 | CH3 | 2-乙氧羰基 -C6H4 | 丙炔-3-基 |
2103 | CH3 | 2-乙氧羰基 -C6H4 | 3-甲基-丁-2-烯-1-基 |
2104 | CH3 | 3-乙氧羰基 -C6H4 | H |
2105 | CH3 | 3-乙氧羰基 -C6H4 | CH3 |
2106 | CH3 | 3-乙氧羰基 -C6H4 | C2H5 |
2107 | CH3 | 3-乙氧羰基 -C6H4 | n-C3H7 |
2108 | CH3 | 3-乙氧羰基 -C6H4 | i-C3H7 |
2109 | CH3 | 3-乙氧羰基 -C6H4 | n-C4H9 |
2110 | CH3 | 3-乙氧羰基 -C6H4 | t-C4H9 |
2111 | CH3 | 3-乙氧羰基 -C6H4 | n-C6H13 |
2112 | CH3 | 3-乙氧羰基 -C6H4 | 丙-1-烯-3-基 |
2113 | CH3 | 3-乙氧羰基 -C6H4 | (E)-1-氯丙-1-烯-3-基 |
2114 | CH3 | 3-乙氧羰基 -C6H4 | 丙炔-3-基 |
2115 | CH3 | 3-乙氧羰基 -C6H4 | 3-甲基-丁-2-烯-1-基 |
2116 | CH3 | 4-乙氧羰基 -C6H4 | H |
2117 | CH3 | 4-乙氧羰基 -C6H4 | CH3 |
2118 | CH3 | 4-乙氧羰基 -C6H4 | C2H5 |
No. | R3 | R4 | R5 |
2119 | CH3 | 4-乙氧羰基 -C6H4 | n-C3H7 |
2120 | CH3 | 4-乙氧羰基 -C6H4 | i-C3H7 |
2121 | CH3 | 4-乙氧羰基 -C6H4 | n-C4H9 |
2122 | CH3 | 4-乙氧羰基 -C6H4 | t-C4H9 |
2123 | CH3 | 4-乙氧羰基 -C6H4 | n-C6H13 |
2124 | CH3 | 4-乙氧羰基 -C6H4 | 丙-1-烯-3-基 |
2125 | CH3 | 4-乙氧羰基 -C6H4 | (E)-1-氯丙-1-烯-3-基 |
2126 | CH3 | 4-乙氧羰基 -C6H4 | 丙炔-3-基 |
2127 | CH3 | 4-乙氧羰基 -C6H4 | 3-甲基-丁-2-烯-1-基 |
2128 | CH3 | 2-氨基羰基 -C6H4 | H |
2129 | CH3 | 2-氨基羰基 -C6H4 | CH3 |
2130 | CH3 | 2-氨基羰基 -C6H4 | C2H5 |
2131 | CH3 | 2-氨基羰基 -C6H4 | n-C3H7 |
2132 | CH3 | 2-氨基羰基 -C6H4 | i-C3H7 |
2133 | CH3 | 2-氨基羰基 -C6H4 | n-C4H9 |
2134 | CH3 | 2-氨基羰基 -C6H4 | t-C4H9 |
2135 | CH3 | 2-氨基羰基 -C6H4 | n-C6H13 |
2136 | CH3 | 2-氨基羰基 -C6H4 | 丙-1-烯-3-基 |
2137 | CH3 | 2-氨基羰基 -C6H4 | (E)-1-氯丙-1-烯-3-基 |
2138 | CH3 | 2-氨基羰基 -C6H4 | 丙炔-3-基 |
No. | R3 | R4 | R5 |
2139 | CH3 | 2-氨基羰基 -C6H4 | 3-甲基-丁-2-烯-1-基 |
2140 | CH3 | 3-氨基羰基 -C6H4 | H |
2141 | CH3 | 3-氨基羰基 -C6H4 | CH3 |
2142 | CH3 | 3-氨基羰基 -C6H4 | C2H5 |
2143 | CH3 | 3-氨基羰基 -C6H4 | n-C3H7 |
2144 | CH3 | 3-氨基羰基 -C6H4 | i-C3H7 |
2145 | CH3 | 3-氨基羰基 -C6H4 | n-C4H9 |
2146 | CH3 | 3-氨基羰基 -C6H4 | t-C4H9 |
2147 | CH3 | 3-氨基羰基 -C6H4 | n-C6H13 |
2148 | CH3 | 3-氨基羰基 -C6H4 | 丙-1-烯-3-基 |
2149 | CH3 | 3-氨基羰基 -C6H4 | (E)-1-氯丙-1-烯-3-基 |
2150 | CH3 | 3-氨基羰基 -C6H4 | 丙炔-3-基 |
2151 | CH3 | 3-氨基羰基 -C6H4 | 3-甲基-丁-2-烯-1-基 |
2152 | CH3 | 4-氨基羰基 -C6H4 | H |
2153 | CH3 | 4-氨基羰基 -C6H4 | CH3 |
2154 | CH3 | 4-氨基羰基 -C6H4 | C2H5 |
2155 | CH3 | 4-氨基羰基 -C6H4 | n-C3H7 |
2156 | CH3 | 4-氨基羰基 -C6H4 | i-C3H7 |
2157 | CH3 | 4-氨基羰基 -C6H4 | n-C4H9 |
2158 | CH3 | 4-氨基羰基 -C6H4 | t-C4H9 |
No. | R3 | R4 | R5 |
2159 | CH3 | 4-氨基羰基 -C6H4 | n-C6H13 |
2160 | CH3 | 4-氨基羰基 -C6H4 | 丙-1-烯-3-基 |
2161 | CH3 | 4-氨基羰基 -C6H4 | (E)-1-氯丙-1-烯-3-基 |
2162 | CH3 | 4-氨基羰基 -C6H4 | 丙炔-3-基 |
2163 | CH3 | 4-氨基羰基 -C6H4 | 3-甲基-丁-2-烯-1-基 |
2164 | CH3 | 2-(N-甲氨基羰基)-C6H4 | H |
2165 | CH3 | 2-(N-甲氨基羰基)-C6H4 | CH3 |
2166 | CH3 | 2-(N-甲氨基羰基)-C6H4 | C2H5 |
2167 | CH3 | 2-(N-甲氨基羰基)-C6H4 | n-C3H7 |
2168 | CH3 | 2-(N-甲氨基羰基)-C6H4 | i-C3H7 |
2169 | CH3 | 2-(N-甲氨基羰基)-C6H4 | n-C4H9 |
2170 | CH3 | 2-(N-甲氨基羰基)-C6H4 | t-C4H9 |
2171 | CH3 | 2-(N-甲氨基羰基)-C6H4 | n-C6H13 |
2172 | CH3 | 2-(N-甲氨基羰基)-C6H4 | 丙-1-烯-3-基 |
2173 | CH3 | 2-(N-甲氨基羰基)-C6H4 | (E)-1-氯丙-1-烯-3-基 |
2174 | CH3 | 2-(N-甲氨基羰基)-C6H4 | 丙炔-3-基 |
2175 | CH3 | 2-(N-甲氨基羰基)-C6H4 | 3-甲基-丁-2-烯-1-基 |
2176 | CH3 | 3-(N-甲氨基羰基)-C6H4 | H |
2177 | CH3 | 3-(N-甲氨基羰基)-C6H4 | CH3 |
2178 | CH3 | 3-(N-甲氨基羰基)-C6H4 | C2H5 |
No. | R3 | R4 | R5 |
2179 | CH3 | 3-(N-甲氨基羰基)-C6H4 | n-C3H7 |
2180 | CH3 | 3-(N-甲氨基羰基)-C6H4 | i-C3H7 |
2181 | CH3 | 3-(N-甲氨基羰基)-C6H4 | n-C4H9 |
2182 | CH3 | 3-(N-甲氨基羰基)-C6H4 | t-C4H9 |
2183 | CH3 | 3-(N-甲氨基羰基)-C6H4 | n-C6H13 |
2184 | CH3 | 3-(N-甲氨基羰基)-C6H4 | 丙-1-烯-3-基 |
2185 | CH3 | 3-(N-甲氨基羰基)-C6H4 | (E)-1-氯丙-1-烯-3-基 |
2186 | CH3 | 3-(N-甲氨基羰基)-C6H4 | 丙炔-3-基 |
2187 | CH3 | 3-(N-甲氨基羰基)-C6H4 | 3-甲基-丁-2-烯-1-基 |
2188 | CH3 | 4-(N-甲氨基羰基)-C6H4 | H |
2189 | CH3 | 4-(N-甲氨基羰基)-C6H4 | CH3 |
2190 | CH3 | 4-(N-甲氨基羰基)-C6H4 | C2H5 |
2191 | CH3 | 4-(N-甲氨基羰基)-C6H4 | n-C3H7 |
2192 | CH3 | 4-(N-甲氨基羰基)-C6H4 | i-C3H7 |
2193 | CH3 | 4-(N-甲氨基羰基)-C6H4 | n-C4H9 |
2194 | CH3 | 4-(N-甲氨基羰基)-C6H4 | t-C4H9 |
2195 | CH3 | 4-(N-甲氨基羰基)-C6H4 | n-C6H13 |
2196 | CH3 | 4-(N-甲氨基羰基)-C6H4 | 丙-1-烯-3-基 |
2197 | CH3 | 4-(N-甲氨基羰基)-C6H4 | (E)-1-氯丙-1-烯-3-基 |
2198 | CH3 | 4-(N-甲氨基羰基)-C6H4 | 丙炔-3-基 |
No. | R3 | R4 | R5 |
2199 | CH3 | 4-(N-甲氨基羰基)-C6H4 | 3-甲基-丁-2-烯-1-基 |
2200 | CH3 | 2-二甲氨基羰基 -C6H4 | H |
2201 | CH3 | 2-二甲氨基羰基 -C6H4 | CH3 |
2202 | CH3 | 2-二甲氨基羰基 -C6H4 | C2H5 |
2203 | CH3 | 2-二甲氨基羰基 -C6H4 | n-C3H7 |
2204 | CH3 | 2-二甲氨基羰基 -C6H4 | i-C3H7 |
2205 | CH3 | 2-二甲氨基羰基 -C6H4 | n-C4H9 |
2206 | CH3 | 2-二甲氨基羰基 -C6H4 | t-C4H9 |
2207 | CH3 | 2-二甲氨基羰基 -C6H4 | n-C6H13 |
2208 | CH3 | 2-二甲氨基羰基 -C6H4 | 丙-1-烯-3-基 |
2209 | CH3 | 2-二甲氨基羰基 -C6H4 | (E)-1-氯丙-1-烯-3-基1 |
2210 | CH3 | 2-二甲氨基羰基 -C6H4 | 丙炔-3-基 |
2211 | CH3 | 2-二甲氨基羰基 -C6H4 | 3-甲基-丁-2-烯-1-基 |
2212 | CH3 | 3-二甲氨基羰基 -C6H4 | H |
2213 | CH3 | 3-二甲氨基羰基 -C6H4 | CH3 |
2214 | CH3 | 3-二甲氨基羰基 -C6H4 | C2H5 |
2215 | CH3 | 3-二甲氨基羰基 -C6H4 | n-C3H7 |
2216 | CH3 | 3-二甲氨基羰基 -C6H4 | i-C3H7 |
2217 | CH3 | 3-二甲氨基羰基 -C6H4 | n-C4H9 |
2218 | CH3 | 3-二甲氨基羰基 -C6H4 | t-C4H9 |
No. | R3 | R4 | R5 |
2219 | CH3 | 3-二甲氨基羰基 -C6H4 | n-C6H13 |
2220 | CH3 | 3-二甲氨基羰基 -C6H4 | 丙-1-烯-3-基 |
2221 | CH3 | 3-二甲氨基羰基 -C6H4 | (E)-1-氯丙-1-烯-3-基 |
2222 | CH3 | 3-二甲氨基羰基 -C6H4 | 丙炔-3-基 |
2223 | CH3 | 3-二甲氨基羰基 -C6H4 | 3-甲基-丁-2-烯-1-基 |
2224 | CH3 | 4-二甲氨基羰基 -C6H4 | H |
2225 | CH3 | 4-二甲氨基羰基 -C6H4 | CH3 |
2226 | CH3 | 4-二甲氨基羰基 -C6H4 | C2H5 |
2227 | CH3 | 4-二甲氨基羰基 -C6H4 | n-C3H7 |
2228 | CH3 | 4-二甲氨基羰基 -C6H4 | i-C3H7 |
2229 | CH3 | 4-二甲氨基羰基 -C6H4 | n-C4H9 |
2230 | CH3 | 4-二甲氨基羰基 -C6H4 | t-C4H9 |
2231 | CH3 | 4-二甲氨基羰基 -C6H4 | n-C6H13 |
2232 | CH3 | 4-二甲氨基羰基 -C6H4 | 丙-1-烯-3-基 |
2233 | CH3 | 4-二甲氨基羰基 -C6H4 | (E)-l-氯丙-1-烯-3-基y1 |
2234 | CH3 | 4-二甲氨基羰基 -C6H4 | 丙炔-3-基 |
2235 | CH3 | 4-二甲氨基羰基 -C6H4 | 3-甲基-丁-2-烯-1-基 |
化合物I适合作杀真菌剂。
化合物I具有非常优异的广谱抗植物病原真菌活性,特别是对子囊菌纲和担子菌纲类病原真菌。它们在某些情况下有系统活性,可用作叶片和土壤的抗真菌药。
它们对于控制多种农作物如小麦、黑麦、大麦、燕麦、水稻、玉米、大麻、棉花、大豆、咖啡、甘蔗、葡萄、水果和装饰植物和蔬菜类植物如黄瓜、豆类、南瓜上和这些植物的种子上的多种病原真菌有特别重要的作用。
它们特别适合控制以下植物疾病:谷物的禾白粉菌(powderymildew),南瓜的二孢白粉菌和苍耳单丝壳菌,苹果的苹果白粉病柄球菌,葡萄树上的钩丝壳属板口线虫,谷物的柄锈属类真菌,棉花和草上的丝核菌属类真菌,谷物和甘蔗上的黑粉菌类,苹果上的苹果黑星菌(scab),谷物的长蠕孢属类、小麦的小麦颖枯病菌,草霉葡萄树上的灰质葡萄球菌(gvad mold),地栗
蒿的花生尾孢,小麦、大麦上的Pseuddocercosporella herpotrichoids,水稻的Pyricularia oryzae,土豆和西红柿的蔓延疫霉,多种植物上的镰孢属菌和轮枝孢菌,葡萄树上的葡萄生单轴霉,蔬菜和水果上的交链孢菌。
化合物I用于杀灭植物、种子或原材料中的真菌,或用达到杀菌效力的活性成分保护土壤免受有害真菌的侵害。它们在真菌感染原材料、植物或种子之前或之后施用。
它们可以转化成常用的剂型,如溶液、乳液、悬浮液、粉尘剂、粉末剂、糊剂或颗粒剂。用什么样的剂型决定于在什么场合使用;但无论如何得保证在环丙烷甲酸邻取代苯甲酯有极细和均一的分散。剂型用众所周知的方法制备,例如使用溶剂和/或用载体,如果需要,使用乳化剂或分散剂,混入活性化合物中,用水作稀释剂时也可使用其它有机溶剂作为辅助溶剂。用于此目的适合的辅助物质主要包括:溶剂如芳香族化合物(如二甲苯),氯化芳香族化合物(如氯苯),链烷烃(如石油馏分),醇(如甲醇、丁醇),酮(如环己酮),胺(如乙醇胺、二甲基甲酰胺)和水;载体物质如自然界中的矿物(如高岭土、陶土、滑石粉、白垩土)和合成物质(如高分散硅酸、硅酸盐);乳化剂如非离子和阴离子乳化剂(如聚氧乙烯脂肪醇醚、烷基磺酸盐和芳基磺酸盐);和分散剂如木质素-亚硫酸盐废液和甲基纤维素。
杀真菌组合物-般含0.1到95%、优选0.5到90%重量的活性化合物。
取决于所需的作用类型,使用量为每公顷0.01到2.0Kg活性化合物。
在种子的处理中,每公斤种子-般需要活性化合物0.001到0.1g,优选0.01到0.05g。
本发明的组合物也可做为杀真菌剂与其它活性物质一起使用,如可以和除草剂、杀虫剂、生长调节剂、杀菌剂或可与肥料一起使用。
与其它杀真剂混合时,在多数情况下增加了杀菌范围。
以下为可和本发明化合物一起使用的杀菌剂,它是用来说明组合的可能性的,但不仅限于它们:
硫,二硫代氨基甲酸盐和它们的衍生物、如二甲氨基二硫代甲酸铁、二甲氨基二硫代甲酸锌、亚乙基双-二硫代氨基甲酸锌、亚乙基双-二硫代氨基甲酸锰、乙二胺双-二硫代氨基甲酸锰锌、二硫化四甲基秋兰姆、(N,N-亚乙基双二硫代氨基甲酸)锌氨配合物、(N,N’-亚丙基双二硫代氨基甲酸)锌氨配合物、(N,N’-亚丙基双二硫代氨基甲酸)锌、N,N’-多亚丙基双(氨基硫羰基)二硫化物;
硝基衍生物,如巴豆酸二硝基(1-甲基庚基)苯基酯,3,3-二甲基丙烯酸2-仲-丁基-4,6-二硝基苯基酯,异丙基碳酸2-仲-丁基-4,6-二硝基苯基酯,5-硝基异邻苯二甲酸二异丙基酯;
杂环化合物,如2-十七烷基-2-咪唑啉乙酸酯,2,4-二氯-6-10-氯苯胺基-5-三嗪,O,O-二乙基苯二(甲)酰亚氨基膦酰基硫代硫酸盐,5-氨基-1-〔双(二甲基氨基)-氧膦基〕-3-苯基-1,2,4-三唑,2,3-二氰基-1,4-二硫代蒽醌,2-硫代-1,3-二硫杂环戊二烯并〔4,5-b〕喹喔啉,1-(丁基氨基甲酰基)-2-苯并咪唑氨基甲酸甲酯,2-甲氧羰基氨基苯并咪唑,2-(呋喃-2-基)苯并咪唑,2-(噻唑-4-基)苯并咪唑,N-(1,1,2,2-四氯乙硫基)四氢邻苯二甲酰亚胺,N-三氯甲硫基四氢邻苯二甲酰亚胺,N-三氯甲硫基邻苯二甲酰亚胺;
N-二氯-氟甲硫基-N’,N’-二甲基-N-苯基磺酰胺,5-乙氧基-3-三氯甲基-1,2,3-噻二唑,2-硫氰基甲硫基苯并噻唑,1,4-二氯-2,5-二甲氧基苯,4-(2-氯苯基亚肼基)-3-甲基-5-异噁唑酮,吡啶-2-硫-1-氧化物,8-羟基喹啉或其铜盐,2,3-二氢-5-甲酰苯胺基-6-甲基-1,4-氧硫杂环己二烯,2,3-二氢-5-N-甲酰苯胺基-6-甲基1,4-氧硫杂环己二烯-4,4-二氧化物,2-甲基-5,6-二氢-4H-吡喃-3-N-甲酰苯胺,2-甲基呋喃-3-N-甲酰苯胺,2,5-二甲基呋喃-3-N-甲酰苯胺,2,4,5-三甲基呋喃-3-N-甲酰苯胺,N-环己基-2,5-二甲基呋喃-3-甲酰胺,N-环己基-N-甲氧基-2,5-二甲呋喃-3-甲酰胺,2-甲基-N-苯甲酰苯胺,2-碘-N-苯甲酰苯胺,N-甲酰基-N-吗啉-2,2,2-三氯乙基乙缩醛,哌嗪-1,4-二基-双(1-(2,2,2-三氯乙基))甲酰胺,1-(3,4-二氯苯胺基)-1-甲酰基-2,2,2-三氯乙烷,2,6-二甲基-N-十三烷基吗啉或其盐,2,6-二甲基-N-环十二烷基吗啉或其盐,N-〔3-(P-叔-丁基苯基)-2-甲基丙基〕-顺-2,6-二甲基吗啉,N-〔3-(P-叔丁基苯基)-2-甲基丙基〕哌啶,1-〔2-(2,4-二氯苯基)-4-乙基-1,3-二氧戊环-2-基-乙基〕-1H-1,2,4-三唑,1-〔2-(2,4-二氯苯基)-4-正丙基-1,3-二氧戊环-2-基乙基〕-1H-1,2,4-三唑,N-(正-丙基)-N-(2,4,6-三氯苯氧乙基)-N’-咪唑基脲,1-(4-氯苯氧基)-3,3-二甲基-1-(1H-1,2,4-三唑-1-基)-2-丁酮,1-(4-氯苯氧基)-3,3-二甲基-1-(1H-1,2,4-三唑-1-基)-2-丁醇,α-(2-氯苯基)-α-(4-氯苯基)-5-嘧啶甲醇,5-丁基-2-二甲氨基-4-羟基-6-甲基嘧啶,双(p-氯苯基)-3-吡啶甲醇,1,2-双(3-乙氧羰基-2-硫脲基)苯,1,2-双(3-甲氧羰基-2-硫脲基)苯,以及各种其他杀真菌剂,如十二烷基胍乙酸盐,3-〔3-(3,5-二甲基-2-氧代环己基)-2-羟乙基〕戊二酰亚胺,六氧苯,DL-甲基-N-(2,6-二甲苯基)-N-2-呋喃甲酰氨基丙酸酯,PL-N-(2,6-二甲苯基)-N-(2’-甲氧乙酰基)丙氨酸甲酯,N-(2,6-二甲苯基)-N-氯乙酰基-D,L-2-氨基丁丙酯,DL-N-(2,6-二甲苯基)-N-(苯基乙酰基)丙氨酸甲酯,5-甲基-5-乙烯基-3-(3,5-二氯苯基)-2,4-二氧代-1,3-噁唑烷,3-〔3,5-二氯苯基-(5-甲基-5-甲氧甲基〕-1,3-噁唑烷-2,4-二酮〔Sil〕,3-(3,5-二氯苯基)-1-异丙基氨基甲酰基海因,N-(3,5-二氯苯基)-1,2-甲基环丙烷-1,2-二甲酰亚胺,2-氰基-〔N-乙氨基羰基-2-甲氧基亚胺基〕乙酰胺,1-〔2-(2,4-二氯苯基)戊基〕-1H-1,2,4-三唑,2,4-二氟-α-(1H-1,2,4-三唑基-1-甲基)二苯甲基醇,N-(3-氯-2,6-二硝基-4-三氟甲苯基)-5-三氟甲基-3-氯-2-氨基吡啶,1-((双(4-氟苯基)甲硅烷基)甲基)-1H-1,2,4-三唑。
式I的化合物还适合控制昆虫、蛛形纲和线虫类害虫,它们也可在植物保护和卫生学中、物品贮存保护和兽医学中用作杀虫剂。
有害昆虫包括蝶类(鳞翅目),如小地老虎,黄地老虎,棉叶波纹夜蛾,黎豆夜蛾,苹实巢蛾,丫纹夜蛾,松尺蠖,Cacoecia Murinana,Capua reticulana,冬尺蛾,云杉卷叶蛾,西方云杉卷叶蛾,美洲粘虫,苹果蠹蛾,欧洲松毛虫,瓜野螟,巨座玉米螟,埃及金钢钻,小玉米螟,Eupoecilia ambiguella,欧洲松梢小卷蛾,粒肤地老虎,大蜡螟,李小食心虫,梨小食心虫,棉铃虫,美洲菸夜蛾,美洲棉铃虫,菜螟,Hiberniadefoliaria,美国白蛾,苹果巢蛾,番茄蠹蛾,铁杉尺蠖,甜菜夜蛾,咖啡-点潜蛾,旋纹潜叶蛾,Lithcalletis blancardella,Lobesia botrana,黄绿条螟,舞毒蛾,僧尼毒蛾,窄翅潜蛾,天幕毛虫,甘蓝夜蛾,花旗松毒蛾,欧洲玉米螟,小眼夜蛾,红铃虫,豆杂角夜蛾,圆掌舟蛾,马铃薯块茎蛾,桔叶潜蛾,大菜粉蝶,苜蓿绿夜蛾,小菜蛾,大豆夜蛾,松梢卷叶蛾,Scrobipalpula absoluta,麦蛾,葡萄长须卷叶蛾、草地粘虫,Spodoptera littoralis,斜纹夜蛾,Thaumatpoea pityocampa,栎绿卷叶蛾,粉纹夜蛾,云杉小卷叶蛾。
甲虫(鞘翅目)如,梨长吉丁,具条叩甲,晦暗叩甲,六月金龟子,李梨木小蠹,棉铃象甲,苹果花象甲,甜菜隐食甲,大松小蠹,Blitophagaundata,蚕豆象,豌豆象,Bruchus lentis,苹果卷叶象甲,Cassidianebulosa,豆叶甲,甘蓝荚象甲,Ceathorrynchus napi,甜菜胫跳甲,烟草金针虫,天门冬叶甲,长角叶甲,Diabrotica 12-punctata,玉米根叶甲,墨西哥豆甲,烟草跳甲,棉籽灰象甲,松树皮象,埃及苜蓿象甲,苜蓿叶象甲,云杉入齿小蠹,烟负泥负,橙足负泥虫,马铃薯甲虫,甜菜叶金针虫,稻象甲,玉米叩甲,油菜花露尾甲,Melolontha hippocastani,Melolontha melolontha,稻负泥虫,Ortiorrhynchus sulcatus,草霉根象甲,辣根猿叶虫,Phyllotrata Chrysocephala,鳃角金角属,庭园丽金龟,芜菁淡足跳甲,黄曲条跳甲,日本丽金龟,豌豆叶象甲,谷象。
双翅目昆虫(piptera),如,埃及伊蚊,骚扰伊蚊,墨西哥桔实蝇,五斑按蚊,地中海实蝇,倍赞氏金蝇,Chrysomya bominivorax,腐败金蝇高梁瘿蚊,嗜人瘤蚊,尖音库蚊,瓜实蝇,油橄榄实蝇,芸苔荚瘿蚊,黄腹厩蝇,大马胃蝇,刺舌蝇,骚扰角蝇,Haplodiplosis equestris,种蝇,纹皮蝇,Liriomyza sativae,Liriomyea trifolii,Lucilia caprina[sic],铜绿蝇,丝光绿蝇,Lycoria pectoralis,小麦瘿蚊,家蝇,厩腐蝇,羊鼻蝇,瑞典麦杆蝇,菠菜潜叶花蝇,Phorbia antiqua,Phorbiabrassicae,Phorbia coarctara,,樱桃实蝇,苹果实蝇,牛虻,Tipulaoleracea,欧洲大蚊。
蓟马(缨翅目昆虫),如烟草褐蓟马,苜蓿蓟马,花蓟马,桔实蓟马,稻蓟马,槽黄蓟马,棉蓟马。
膜翅昆虫(膜翅目),如菜叶蜂,热带切叶蚊,切叶蚊,得州切叶蚁,叶蜂,苹实叶蜂,厨蚁,火蚁,外引红火蚁。
臭虫(异翅亚目),如喜绿蝽,多毛长蝽,Cyrtopeltis notatus,棉红蝽,Dysdercus intermedius,Eurygaster integriceps,棉褐蝽,叶足缘蝽,牧草盲蝽,(Lygus lineolaris),牧草盲蝽(Lygus pratensis),稻绿蝽,甜苹拟网蝽,Solubea insularis,Thyanta perditor。
吸食植物汁液的昆虫(同翅目),如驴喜豆无网长管蚜,落叶松球蚜,Aphidula nasturtii,蚕豆蚜,苹果蚜,Aphis sambuci,蓟短尾蚜,甘蓝蚜;Cerosipha gossypii,Dreyfusia nordmanniane,Dreyfusia piceae,Dysaphis radicola,Dysaulacortham pseudosolani,蚕豆微叶蝉,麦长管蚜,大戟长管蚜,蔷薇长管蚜,蚕豆修尾蚜,蔷薇麦蚜,Myzodes persicae,樱桃黑瘤额蚜,稻褐飞虱,莴苣根瘿绵蚜,蔗飞虱,忽布瘤额蚜,苹木虱,梨木虱,Rhopalomyzus ascalonicus,玉米缢管蚜,Sappaphis mala,Sappaphis mali,麦二叉蚜,榆梨绵蚜,温室白粉虱,葡萄根瘤蚜。
白蚁(等翅目昆虫),如Calotermes flaricollis,Leucotermes flavipes,Retieulitermes lucifugas,Termes natalensis。
直翅类昆虫(直翅目),如象蟋蟀,东方蠊,德国小蠊,欧洲球螋,欧洲蝼蚱,飞蝗,双带蚱蜢,赤腿蚱蜢,墨西哥蚱蜢,迁徒蚱蜢,落矶山蚱蜢,红翅蝗,美洲大蠊,美洲蚱蜢,Schistocerca peregrina,Stanronotus maroccanus温室蟋螽。
蛛形纲,例如蛛形害虫(蜱螨目),如美洲花蜱,彩饰花蜱,波斯隐喙蜱,具环方头蜱,褪色牛蜱,微小牛蜱,紫红短须螨,苜蓿苔螨,森林革蜱,鹅耳枥东方叶螨,桔瘿螨,Hyalomma truncatum羊硬蜱,浅红硬蜱,非翅蝇缘蜱,耳残喙蜱,梅旁叶螨,鸡皮刺螨,桔锈螨,侧多食趺线螨,羊痒螨,非洲扇头蜱,Rhipicephalus cvertsi,疥螨,朱砂叶螨,神泽叶螨,太平洋红叶螨,棉红叶螨,棉叶螨。
线虫类,例如根瘿线虫,如北方根结线虫,南方根结线虫,瓜哇根结线虫,曲体线虫,如,马铃薯金线虫,燕麦异皮线虫,大豆异皮线虫,甜菜异皮线虫,三叶草异皮线虫,茎和叶子的小线虫,如,长尾刺线虫,马铃薯茎线虫,起绒草茎线虫,多带螺旋线虫,逸去长针线虫,相似穿孔线虫,强壮盘旋线虫,原始毛刺线虫,克莱顿矮化线虫,不定矮化线虫,落选短体线虫,穿刺短体线虫,pratylenchus curvitatus,左氏短体线虫。
活性化合物可以直接应用,或可以其制剂形式应用,也可以由其制备的施用制剂形式应用,例如以直接可雾化的溶液、粉剂、悬液或分散体、乳剂、油分散剂、糊剂、粉末剂、撒播组合物颗粒剂形式通过喷雾、雾化、撒粉、撒播或浇灌使用,应用形式完全决定于使用目的;而且不论在任何情况下都应尽可能保证本发明的活性化合物有最细的分散度。
活性化合物在为准备应用的制剂中的浓度可在很大范围内改变。
一般地,为从0.0001%到10%,更优选的范围为0.01%到1%。
活性化合物也在超低体积法(ULV)中取得了极大成功,这样就可能应用活性化合物重量比为95%的制剂,甚至可在活性化合物中不加添加剂的情况下应用。
户外控制害虫时活性化合物的应用量为0.1到2.0、更优选为0.2到1.0kg/ha。
在制备可直接雾化的溶液、乳液、糊剂或油分散剂中,适用的载体是:中至高沸点的矿物油馏分,如煤油或柴油,还有煤焦油和来自植物和动物的油,脂肪族、环族和芳烃化合物如苯、甲苯、二甲苯、石蜡、四氢化萘、烷化萘或它们的衍生物,甲醇,乙醇,丙醇,丁醇,氯仿,四氯化碳,环己醇,环己酮,氯苯,异佛尔酮,强极性溶剂如二甲基甲酰胺、二甲亚砜、N-甲基吡咯烷酮和水。
含水剂型可由浓缩乳液、糊剂或可与水混合的粉剂(油分散剂)加入水制备。为制备乳剂、糊剂或油分散剂,可通过增湿剂、增粘剂、分散剂或乳化剂的方法将这些物质与水混合成匀相物质或溶于油或其它溶液中。然而,也可以制备包含有活性物质、增湿剂、增粘剂、分散剂或乳化剂而且可能有溶剂或油的浓缩液,它适于用水稀释。
适合的表面活性剂为木素磺酸、萘磺酸,苯酚磺酸,二丁基萘磺酸,碱金属、碱土金属和铵盐,烷芳基磺酸盐,烷基硫酸盐,烷基磺酸盐,脂肪醇硫酸盐和脂肪酸以及它们的碱金属和碱土金属盐,硫酸化脂族醇乙二醇醚的盐,磺酸化的萘和萘衍生物与甲醛的缩合产物,萘或萘磺酸与酚和甲醛的缩合产物,聚氧乙烯率酚醚,乙氧化异辛基酚、辛基酚、壬基酚,烷基苯酚聚乙二醇醚,三丁基苯基聚乙二醇醚,烷芳基聚醚醇,异十三烷基醇,脂肪醇环氧乙烷缩合物,乙氧化蓖麻油,聚氧乙烯烷基醚,乙氧化聚氧丙烯,月桂醇聚乙二醇醚乙缩醛,山梨醇酯,木质素亚硫酸盐度液和甲基纤维素。
粉剂、撒播组合物和粉尘剂可以混合或将活性化合物与固体载体一起研磨而制备。
制剂一般含有0.0l到95%、更优选为0.1到90%重量活性化合物。在此使用的活性化合物纯度为从90%到100%、更优选为95%到100%(根据NMR谱)。
制剂的示例有:
I.5重量份本发明活性化合物与95重量份极细的高岭土均匀混合。此法得到含5%重量活性物质的粉尘剂。
II.30重量份本发明活性化合物与已在其表面喷淋8重量份石蜡油的92重量份细粉状硅胶混匀。此法制得活性物质有很好的粘着性的产品(含23%重量活性化合物)。
III.将10重量份本发明活性化合物溶于一种混合物中,此种混合物由90重量份二甲苯、6重量份由8到10mol环氧乙烷加合到1mol油酸N-单乙醇酰胺上形成的加合物、2重量份十二烷基苯磺酸的钙盐和2重量份由40mol环氧乙烷加合到1mol蓖麻油上得到的加合物组成(活性化合物含量为9%重量)。
IV.将20重量份本发明活性化合物溶于一种混合物中,此种混合物由60重量份环己酮、30重量份异丁醇、5重量份由7mol环氧乙烷加合到1mol异辛基苯酚上得到的加合物及5重量份由40mol环氧乙烷加合到1mol蓖麻油上制得的加合物组成(活性化合物含量为16%重量)。
V.将80重量份本发明活性化合物与3重量份二异丁基萘-α-磺酸的钠盐、10重量份从亚硫酸盐废液中得到的木素磺酸钠盐及7重量份粉状硅胶混匀,并将混合物在球磨机中磨碎(活性化合物含量为80%重量)。
VI.将90重量份本发明活性化合物与10重量份N-甲基-α-吡咯烷混合,得到一种溶液,此溶液适合于以微小液滴的形式使用(活性化合物含量为90%重量)。
VII.将20重量份本发明化合物溶于一种混合物中,此混合物由40重量份环己酮、30重量份异丁醇、20重量份由7mol环氧乙烷加合到1mol异辛基苯酚上得到的加合物和10重量份由40mol环氧乙烷加合到1mol蓖麻油上得到的加合物组成。将此溶液倾倒并极细地分散于以100000重量份水中,得到一水分散体,它含有0.02%重量计的活性化合物。
VIII.将20重量份的本发明活性化合物与3重量份二异丁基萘-α-磺酸钠、17重量份从亚硫酸盐废液中得到的木质磺酸的钠盐和60重量份粉状硅胶混匀,且将此混合物在球磨机中磨成细粉,将此混合物极细地分散到20,000重量份水中,得到一喷雾剂,其含有0.1%重量的活性化合物。
颗粒剂如涂布、浸渍和均相颗粒,可通过将活性化合物粘合在固体载体上来制备。固体载体例如为:矿物土,如硅胶、硅酸、硅胶、硅酸盐、滑石、高岭土、硅镁土、石灰石、石灰、白垩、红玄武土、黄土、粘土、白云石、硅藻土、硫酸钙和硫酸镁、氧化镁;粉碎的合成物质、肥料,如硫酸铵、磷酸铵、硝酸铵、尿素;和植的产品,如谷物粉、树皮、木或坚果壳粉、纤维素粉;和其它固体载体。
多种类型的油、除草剂、杀真菌剂、其它杀虫剂和杀菌剂可以加入到此活性化合物中,如果仅仅在使用前立即进行(在容器中混匀)合适的活。这些物质可以以1∶10-10∶1的重量比加入到本发明组合物中。
合成实施例:
在下面的合成实例中描述的过程中将原料化合物经适合的方法转化为化合物I,如此得到的化合物及其物理参数列于随后的表中。
实施例1
制备(E,E)-2-甲氧亚氨基-2-〔2’-(1”-甲基,1”-乙酰基)亚氨氧甲基〕苯乙酸甲酯
在保护性气体条件及在室温轻微冷却下,将21g(0.21mol)二乙酰单肟加入到溶有6.4g(0.21mol)氢化钠(80%)的150ml无水二甲基甲酰胺中,将混合物在室温下搅拌30分钟。然后滴加入60g(0.21mol)2-甲氧亚氨基-2-(2’-溴甲基)苯乙酸甲基酯溶于360ml二甲基甲酰胺中的溶液,并将混合物在室温下搅拌16小时。加入10%浓度的盐酸后,用甲基叔丁基醚萃取。将合并的有机相用水洗涤,用Na2SO4干燥并浓缩。将残余物悬浮于少量冷甲醇中,抽滤后,得到38g(59%)标题化合物,为浅棕色结晶,熔点69-71℃。1H-NMR(CDCl3):δ=1.87(s,3H);2.30(s,3H);3.85(s,3H);4.05(s,3H);5.15(s,2H);7.17-7.48(m,4H)ppm.
实施例2
制备(E,E,E-2-甲氧亚氨基-2-〔2’-.(1”-甲基,1”-(1”’-乙氧亚氨基乙基))亚氨基氧甲基〕苯乙酸甲酯
向2.5g(8.2mmol)(E,E)-2-甲氧亚氨基-2-〔2’-(1”-甲基,1”-乙酰基)亚氨基氧甲基〕苯乙酸甲酯于60ml热甲醇中的溶液中,将此溶液冷却到室温后,加入0.96g(9.8mmol)O-乙基羟胺盐酸盐和0.6g分子筛颗粒(3A),并将混合物在室温下放置5天。过滤掉分子筛后,将溶液浓缩,将残余物在甲基叔丁基醚和水之间分配,将有机相用水洗涤,用Na2SO4干燥并浓缩,将残余物用正己烷研磨,抽滤,得到1.8g(63%)标题化合物,为浅黄色结晶,熔点69-72℃。1H-NMR(CDCl3):δ=1.27(t,3H);1.96(s,3H);1.99(s,3H);3.84(s,3H);4.04(s,3H);4.17(q,2H);5.06(s,2H);7.17-7.49(m,4H)ppm
实施例3
制备(E,E,E)-2-甲氧亚氨基-2-〔2’-(11”-甲基,1”-(1”’-羟基亚氨基乙基))亚氨基氧甲基〕苯乙酸甲酯。
将2.0g(17mmol)二乙酰基二肟分批加入到0.60g(20mmol)氢化钠(80%)于14ml无水二甲基甲酰胺中的溶液中,并将此混合物在室温下搅拌30分钟。然后加入5.0g(17mmol)2-甲氧亚氨基-2-(2’-溴甲基)苯乙酸甲酯于30ml二甲基甲酰胺中的溶液,将混合物在室温下搅拌2小时。加入10%浓度的盐酸后,用甲基叔丁基醚萃取。将合并的有机相用水洗涤,用Na2SO4干燥并浓缩。加入甲醇研制残余物后,抽滤出固体,将滤液在旋转蒸发器上浓缩后用色谱柱法在硅胶柱上纯化(甲基叔丁基醚/正己烷),得到1.0g(18%)标题化合物,为白色粉末,熔点107-111℃。1H-NMR(CDCl3):δ= 1.97(s,3H);2.00(s,3H);3.84(s,3H);4.05(s,3H);5.08(s,2H);7.17-7.45(m,4H),8.56(s,1H)ppm.
实施例4
制备4-肟基-2,2-二甲基戊烷-3-酮
室温下,将156g二乙基醚中的40g氯化氢滴加入960g甲苯中的96g(0.84mol)2,2-二甲基-3-戊酮中。冷却到-10℃后,滴加入470g二乙基醚中的95g亚硝酸正丁基酯。将混合物在-10℃至0℃下搅拌4小时,然后升至室温。共计16小时后,将反应混合物每次用1升冰水洗涤,共洗涤三次,然后每次用1升1M氢氧化钠溶液萃取,共萃取2次。分出碱水相并用20%浓度的硫酸中和,将粗产物抽滤干燥后,在正己烷中重结晶。得到66g(55%)标题化合物。为浅黄色粉末,熔点107-110℃。1H-NMR(CDCl3):δ=1.29(s,9H);1.99(s,3H);8.30(s,1H)ppm.
实施例5
制备(E)-2-甲氧亚氨基-2-〔2’-(1”-甲基,1”-(1”’,1”’-二甲基乙基羰基))亚氨基氧甲基〕苯乙酸甲酯
将25g(0.17mol)4-羟基亚氨基-2,2-二甲基戊烷-3-酮在保护气体条件下分批加入到6.4g(0.21mol)氢化钠(80%)溶于150ml无水二甲基甲酰胺的溶液中,将反应物升温至50℃。继续搅拌30分钟,然后滴加入50g(0.17mol)2-甲氧亚氨基-2-(2’-溴甲基)苯乙酸甲酯溶于300ml二甲基甲酰胺的溶液,将混合物在室温下搅拌16小时。加入10%浓度的盐酸后,用甲基叔丁基醚萃取。将合并的有机相用水洗涤,用Na2SO2干燥并浓缩。将黑色的油状残余物用色谱柱法在硅胶柱上纯化(甲基叔丁基醚/正己烷),然后将产品悬浮于冰冷却的醇中,抽滤后得到24g(41%)标题化合物,为几乎无色的粉末,熔点58-62℃。1H-NMR(CDCl3):δ=1.19(s,9H);1.90(s,3H);3.83(s,3H);4.04(s,3H);5.11(s,2H);7.18-7.45(m,4H)ppm.
实施例6
制备(E)-2-甲氧亚氨基-2-〔2’-(1”-甲基,1”-(1”’-(6””-(4””-氯苯基)己氧亚氨基),2”’,2”’-二甲基丙基))亚氨基氧甲基〕苯乙酸甲酯
向3.0g(8.6mmol)(E)-2-甲氧亚氨基-2-〔2’-(1”-甲基,1”-(1”’,1”’-二甲基乙基羰基))亚氨基氧甲基〕苯乙酸甲酯溶于60ml热甲醇中,冷却到室温后,加入5.9g(26mmol)O-6-(4’-氯苯基)己基羟基胺、3.6g无水分子筛颗粒(3A)和1.6g(8.6mmol)对甲苯磺酸水合物,并将此混合物回流3小时。过滤掉分子筛后,将溶液浓缩,将残余物在甲基叔丁基醚与水之间分配,将有机相用水洗涤,用Na2SO4干燥并浓缩。用色谱柱法在硅胶柱上纯化(己烷/甲基叔丁基醚)后,得到3.8g(79%)标题化合物,为浅黄色油。1H-NMR(CDCl3):δ=1.09(s,9H);1.26-1.42(m,4H);1.52-1.67(m,4H);1.90(s,3H);2.57(t,2H);3.84(s,3H);3.99(t,2H);4.03(s,3H);5.02(s,2H);7.07-7.47(m,8H)ppm.
实施例7
制备(E)-2-甲氧基亚氨基-2-〔2’-(1”-甲基,1”-甲氧基羰基)亚氨基氧甲基〕苯乙酸甲酯
将6.1g(52mmol)2-羟基亚氨基丙酸甲酯分批加入到2.0g(67mmol)氢化钠(80%)溶于100ml无水二甲基甲酰胺形成的溶液中,将此反应混合物加热到50℃。继续搅拌30分钟,然后将15g(52mmol)2-甲氧亚氨基-2-(2’-溴甲基)苯乙酸甲酯溶于90ml二甲基甲酰胺形成的溶液滴加到此混合液中,并在室温下搅拌16小时。加入10%浓度的盐酸后,用甲基叔丁基醚萃取。将合并的有机相用水洗涤,用Na2SO4干燥并浓缩。将残余物悬浮于冰冷却的甲醇中,抽滤后得到7.2g(43%)标题化合物,为米黄色粉末,熔点78-82℃。1H-NMR(CDCl3):δ=2.04(s,3H);3.85(s,3H);3.86(s,3H);5.19(s,2H);7.16-7.49(m,4H)ppm.
实施例8
制备2-〔2’-(1”-甲基,1”-(1”’-甲氧亚氨基,1”’-苯基)甲基)亚氨基氧甲基〕苯基-3-甲氧基-丙-E-2-烯酸甲酯
将2.4g(28mmol)O-甲基羟基胺盐酸盐和3g无水分子筛(3A)加入到2.5g(7mmol)2-〔2’-(1”-甲基,1”-苯甲酰基)亚氨基氧甲基〕-苯基-3-甲氧基丙-E-2-烯酸甲酯溶于100ml甲醇的溶液中。此反应混合物在室温下放置3天,然后在60℃搅拌8小时。
过滤掉分子筛后,将溶液加入到200ml水中,并将此混合物用甲基叔丁基醚萃取。
将合并的有机相用水洗涤,用Na2SO4干燥并浓缩,用色谱柱法在硅胶柱上纯化(正己烷/甲基叔丁基醚9∶1)后,得到1.1g(40%)标题化合物,为异构体的混合物(在侧链上异构,异构体1∶10),为无色油状物。IR[cm-1](膜)768,1036,1057,1111,1130,1190,1256,1284,1634,1709,2930
实施例9
将1g(11.4mmol)O-甲基羟胺盐酸盐和2g无水分子筛(3A)加入到1g(2.9mmol)α-〔2’-(1”-甲基,1”-苯甲酰基)亚氨基氧甲基〕苯基-E-β-甲基丙烯酸甲酯溶入到50ml甲醇形成的溶液中。将此溶液首先在室温下放置2小时,然后升温到60℃保持6小时。过滤掉分子筛后,加入水并将此混合物用甲基叔丁基醚萃取,将合并的有机相用水洗涤,用Na2SO4干燥并浓缩。
在硅胶柱上用色谱法纯化(正己烷/甲基叔丁醚9∶1)后,得到0.9g(85%)标题化合物,以异构体混合物形式存在(1∶1,侧链异构),为无色油状物。IR[cm-1](膜):693,764,872,892,1005,1035,1207
1253,1435,1716,2920
实施例10
(E)-2-甲氧亚氨基-2-〔2’-(1”-甲基,1”-(1”’(Z)-甲氧亚氨基,1”’-苯基)甲基)(E)-亚氨基氧甲基〕苯乙酯甲酯(表I化合物I.48)异构化成(E)-2-甲氧基亚氨基-2-〔2’-(1”-甲基,1”-(1”’-(E)-甲氧亚氨基,1”’-苯基)甲基〕(E)-亚氨基氧甲基〕苯乙酸甲酯:
将46g初始化合物悬浮于600ml乙醚中,用200ml饱和醚·HCl处理,在室温下放置19小时。将反应液加入到冰水中并用二氯甲烷萃取,将萃取液用Na2SO4干燥,在旋转蒸发仪上浓缩后,得到油状残余物,在甲醇中结晶,得到所需的(E,E,E)异构体,为白色固体(35g,产率=75%)。
熔点:118-120℃(95%E,E,E)表I
表II
表III
No. | R2 m | R3 | R4 | R5 | 数据 |
I.13 | H | CH3 | CH3 | 6-(4’-氯苯基)己-1-基 | 油;1H-NMR(CDCl3):δ=1.26-1.70(m,8H);1.94(s,3H);1.98(s,3H);2.56(t,2H);3.84(s,3H);4.03(s,3H);4.10(t,2H);5.06(s,2H);7.08-7.50(m,8H)ppm |
I.14 | H | CH3 | CH3 | 2,4-(NO2)2-C6H3 | m.p.:158-161℃ |
I.15 | H | CH3 | CH3 | 3-CF3-C6H4 | m.p.:77-79℃ |
I.16 | H | CH3 | CH3 | 4-CF3,6-Cl-吡啶-2-基 | m.p.:134-137℃ |
I.17 | H | CH3 | CH3 | 4-CF3-吡啶-2-基 | m.p.:92-95℃ |
I.18 | H | CH3 | CH3 | 6-Cl-嘧啶-4-基 | m.p.:110-120℃ |
I.19 | H | CH3 | CH3 | (E)-1--氯丙烯-3-基 | m.p.:76-78℃ |
I.20 | H | CH3 | CH3 | (E)-4-(4’-氯苯基)-5-2-烯-1-基 | m.p.:69-73℃ |
I.21 | H | CH3 | CH3 | 丙炔-3-基 | m.p.:119-121℃ |
I.22 | H | CH3 | CH3 | 2-羟基-丙-1-基 | m.p.:74-79℃ |
I.23 | H | CH3 | CH3 | 6-羟基-2-甲基-嘧啶-4-基甲基 | m.p.:189-194℃ |
I.24 | H | CH3 | CH3 | 6-羟基-2-异丙基-嘧啶-4-基甲基 | m.p.:180-187℃ |
I.25 | H | CH3 | CH3 | 6-羟基-2-环丙基-嘧啶-4-基甲基 | m.p.:190-193℃ |
I.26 | H | CH3 | CH3 | 5-(2′-呋喃)-戊-1-基 | m.p.:36-40℃ |
I.27 | H | CH3 | CH3 | 5-(2’-N-甲基吡咯)-戊-1-基 | m.p.:40-44℃ |
I.28 | H | CH3 | CH3 | 2-(4’-氯苯基)-噁唑-4-基甲基 | m.p.:110-115℃ |
I.29 | H | CH3 | CH3 | 3-三氟甲基吡啶-2-基 | m.p.:112-115℃ |
I.30 | H | CH3 | CH3 | 5-三氟甲基吡啶-2-基 | m.p.:110-115℃ |
No. | R2 m | R3 | R4 | R5 | 数据 |
I.31 | H | CH3 | CH3 | 6-(2’-噻吩)-己-1-基 | IR[cm-1]:893,958,988,1021,1049,1070,1219,1365,1729,2935 |
I.32 | H | CH3 | t-C4H9 | H | m.p.:114-117℃ |
I.33 | H | CH3 | t-C4H9 | CH3 | m.p.:51-55℃ |
I.34 | H | CH3 | t-C4H9 | C2H5 | 油;IR(膜):2972,2955,1729,1364,1219,1069,1044,1020,957 |
I.35 | H | CH3 | t-C4H9 | i-C3H7 | 油;IR(膜):2972,2937,1729,1366,1323,1218,1070,1047,1020,962 |
I.36 | H | CH3 | t-C4H9 | n-C4H9 | 油;IR(膜):2957,2935,2872,1929,1437,1364,1218,1069,1020,959 |
I.37 | H | CH3 | t-C4H9 | t-C4H9 | 油;IR(膜):2973,1730,1364,1218,1195,1069,1047,1020,956,916 |
I.38 | H | CH3 | t-C4H9 | n-C6H13 | 油;IR(膜):2955,2933,2870,1729,1364,1218,1069,1049,1020,958 |
I.39 | H | CH3 | t-C4H9 | (E)-1-氯丙烯-3-基 | 油;IR(膜):2955,1729,1437,1365,1219,1069,1046,1020,959,915 |
I.40 | H | CH3 | t-C4H9 | 丙炔-3-基 | 油;IR(膜):3300,2955,1729,1437,1365,1321,1219,1069,1020,1006,916 |
I.41 | H | CH3 | t-C4H9 | 3-甲基-丁-2-烯-1-基 | 油;IR(膜):2968,2954,1729,1437,1218,1069,1046,1019,985,918 |
I.42 | H | CH3 | t-C4H9 | 2-萘基-CH2 | 油;IR(膜):2954,1728,1437,1365,1219,1069,1019,958,921,896 |
I.43 | H | CH3 | t-C4H9 | 4-Cl-C6H4-CH2 | 油;IR(膜):2960,1728,1491,1365,1218,1089,1069,1015,988,919,881 |
I.44 | H | CH3 | t-C4H9 | (E)-4-(4’-氯苯基)丁-2-烯-1-基 | 油;IR(膜):2963,1728,1491,1365,1218,1093,1069,1048,1016,983,960 |
No. | R2 m | R3 | R4 | R5 | 数据 |
I.45 | H | CH3 | t-C4H9 | 6-(4’-氯苯基)己-1-基 | 油;IR(膜):2934,1729,1492,1364,1218,1092,1069,1048,1016,958 |
I.46 | H | CH3 | t-C4H9 | 3-CF3-C6H4 | 油;IR(膜):2980,1729,1450,1331,1214,1169,1127,1069,1020,941,928 |
I.47 | H | CH3 | C6H5 | H | m.p.:139-143℃ |
I.48 | H | CH3 | C6H5 | CH3 | m.p.:71-75℃ |
I.49 | H | CH3 | C6H5 | C2H5 | m.p.:65-70℃ |
I.50 | H | CH3 | C6H5 | i-C3H7 | m.p.:83-87℃ |
I.51 | H | CH3 | C6H5 | n-C4H9 | 油;IR(膜):2956,2937,1728,1219,1201,1069,1046,1019,978,959 |
I.52 | H | CH3 | C6H5 | 4-Cl-C6H4-CH2 | m.p.:88-93℃ |
I.53 | H | CH3 | C6H5 | 3-CF3-C6H4 | 油;IR(膜):2940,1729,1450,1329,1281,1219,1169,1126,1069,1021,957 |
I.54 | H | CH3 | C6H5 | 6-(4’-氯苯基)己-1-基 | 油;IR(膜):2935,1732,1492,1444,1437,1219,1069,1015,985,959 |
I.55 | H | CH3 | C6H5 | (E)-4-(4’-氯苯基)丁-2-烯-1-基 | 油;IR(膜):2945,1727,1491,1444,1437,1219,1201,1069,1047,1015,974 |
I.56 | H | C6H5 | C6H5 | CH3 | IR[cm-1](KBr):692,766,958,986,1018,1051,1069,1221,1445,1727,2940 |
I.57 | H | C6H5 | C6H5 | C2H5 | 油;IR[cm-1](膜):693,766,959,985,1019,1050,1069,1221,1445,1728,2940 |
I.58 | H | C6H5 | C6H5 | n-C3H7 | 油;IR[cm-1](膜);693,766,962,987,1020,1068,1221,1445,1728,2930 |
I.59 | H | C6H5 | C6H5 | i-C3H7 | 油;IR[cm-1](膜):693,766,978,1019,1069,1121,1220,1323,1445,1728,2960 |
No. | R2 m | R3 | R4 | R5 | 数据 |
I.60 | H | C6H5 | C6H5 | n-C4H9 | 油;IR[cm-1](膜):693,960,975,120,1069,1220,1445,1728,2956 |
I.61 | H | C6H5 | C6H5 | t-C4H9 | 油;IR[cm-1](膜):694,961,971,1019,1069,1190,1220,1364,1445,1728,2960 |
I.62 | H | C6H5 | C6H5 | n-C6H13 | 油;IR[cm-1](膜):693,959,986,1019,1069,1220,1445,1728,2935,2952 |
I.63 | H | C6H5 | C6H5 | 3-甲基-丁-2-烯-1-基 | 油;IR[cm-1](膜):693,766,958,986,1019,1069,1220,1444,1728,2930 |
I.64 | H | CH3 | CH3 | 4-苯基-丁-1-基 | m.p.:64-66℃ |
I.65 | H | CH3 | CH3 | 4-苯氧基-丁-1-基 | 油;IR[cm-1](膜):755,890,987,1020,1049,1070,1220,1245,1498,1728,2940 |
I.66 | H | CH3 | CH3 | 2-(2’-氟苯氧基)乙-1-基 | 油;IR[cm-1](膜):749,1020,1036,1051,1070,1205 1219,1260,1507,1728,2940 |
I.67 | H | CH3 | CH3 | 3-(2′-氟苯氧基)-丙-1-基 | m.p.:53-56℃ |
I.68 | H | CH3 | CH3 | 4-(2’-氟苯氧基)-丁-1-基 | m.p.:47-50℃ |
I.69 | H | CH3 | CH3 | 6-(4’-氯苯氧基)己-1-基 | 油;IR[cm-1](膜):890,1020,1047,1070,1219,1244,1366,1492,1728,2939 |
I.70 | H | CH3 | CH3 | 2-(4’-氯苯氧基)丙-1-基 | 油;IR[cm-1](膜):886,958,1020,1049,1070,1220,1241,1366,1490,1728,2920 |
I.71 | H | CH3 | CH3 | C6H5-C2H4-O-C2H4 | 油;IR[cm-1](膜):893,958,984,1020,1049,1069,1120,1219,1366,1728,2940 |
I.72 | H | CH3 | CH3 | E-4-(3’-甲氧苯基)-丁-3-烯-1-基 | 油;IR[cm-1](膜):890,959,1020,1046,1070,1219,1266,1366,1436,1728,2940 |
No. | R2 m | R3 | R4 | R5 | 数据 |
I.101 | H | CH3 | 4-Cl-C6H4 | n-C6H13 | 油;IR(膜):958,1020,1070,1091,1219,1491,1729,2935,2953 |
I.102 | H | CH3 | 4-Cl-C6H4 | 3-甲基-丁-2-烯-1-基 | 油;IR(膜):960,1019,1069,1219,1437,1491,1728,2930 |
I.103 | H | CH3 | 4-Cl-C6H4 | 炔丙基 | 油;IR(膜):958,1009,1069,1092,1220,1437,1491,1728,2120,2930,3280 |
I.104 | H | CH3 | 4-F-C6H4 | CH3 | m.p.:104-107℃ |
I.105 | H | CH3 | 4-F-C6H4 | C2H5 | 油;IR(膜):841,957,1020,1069,1222,1438,1509,1728,2930 |
I.106 | H | CH3 | 4-F-C6H4 | n-C3H7 | 油;IR(膜):959,989,1020,1069,1222,1437,1509,1728,2930 |
I.107 | H | CH3 | 4-F-C6H4 | i-C3H7 | m.p.:66-71℃ |
I.108 | H | CH3 | 4-F-C6H4 | t-C4H9 | m.p.:76-81℃ |
I.109 | H | CH3 | 4-F-C6H4 | n-C4H9 | 油;IR(膜):959,980,1020,1070,1222,1509,1729,2938,2957 |
I.110 | H | CH3 | 4-F-C6H4 | n-C6H13 | 油;IR(膜):958,986,1020,1070,1222,1509,1729,2935,2953 |
I.111 | H | CH3 | 4-F-C6H4 | 3-甲基-丁-2-烯-1-基 | 油;IR(膜):841,960,986,1019,1069,1222,1508,1728,2930 |
I.112 | H | CH3 | 4-F-C6H4 | 炔丙基 | m.p.:83-88℃ |
I.113 | H | CH3 | 4-Cl-C6H4 | H | m.p.:137-140℃ |
I.114 | H | CH3 | 4-Cl-C6H4 | (2-甲基-噻唑-4-基)-甲基 | m.p.:128-133℃ |
I.115 | H | CH3 | 4-Cl-C6H4 | (噻唑-4-基)-甲基 | m.p.:93-97℃ |
No. | R2 m | R3 | R4 | R5 | 数据 |
I.116 | H | CH3 | 4-Cl-C6H4 | (3-异丙基-1,2,4-噁二唑-5-基)-甲基 | 油;IR(膜):874,958,1018,1069,1091,1220,1491,1589,1728,2960 |
I.117 | H | CH3 | 4-Cl-C6H4 | (3-异丙基-异噁唑-5-基)-甲基 | 油;IR(膜):959,986,999,1021,1070,1092,1220,1437,1491,1728,2960 |
I.118 | H | CH3 | 4-Cl-C6H4 | (3-溴-异噁唑-5-基)-甲基 | 油;IR(膜):952,1014,1069,1092,1201,1219,1334,1362,1436,1727,2930 |
I.119 | H | CH3 | 4-Cl-C6H4 | (3-CF3-异噁唑-5-基)-甲基 | 油;IR(膜):970,1016,1070,1092,1155,1192,1219,1491,1728,2930 |
I.120 | H | CH3 | 3-Cl-C6H4 | CH3 | m.p.:78-81℃ |
I.121 | H | CH3 | C2H5 | CH3 | m.p.:88-91℃ |
I.122 | H | CH3 | C2H5 | C2H5 | m.p.:60-65℃ |
I.123 | H | CH3 | 4-CH3-C6H4 | CH3 | 油;IR(膜):958,1020,1036,1069,1200,1220,1321,1438,1728,2939 |
I.124 | H | CH3 | 4-CH3-C6H4 | C2H5 | 油;IR(膜):922,957,983,1020,1069,1220,1438,1729,2940 |
I.125 | H | CH3 | 4-CH3-C6H4 | n-C3H7 | 油;IR(膜):959,988,1020,1070,1219,1437,1729,2939,2965 |
I.126 | H | CH3 | 3-Cl-C6H4 | i-C3H7 | 油;IR(膜):959,980,1020,1070,1120,1201,1219,1324,1729,2940,2980 |
I.127 | H | CH3 | 3-Cl-C6H4 | n-C4H9 | 油;IR(膜):959,980,1020,1070,1201,1219,1729,2938,2956 |
I.128 | H | CH3 | 3-Cl-C6H4 | 3-氯丙-2-烯-1-基 | m.p.:73-75℃ |
I.129 | H | CH3 | 3-Cl-C6H4 | 炔丙基 | 油;IR(膜):928,958,1010,1049,1069,1201,1220,1322,1437,1728,2110,2930,3280 |
No. | R2 m | R3 | R4 | R5 | 数据 |
I.130 | H | CH3 | 2-Cl-C6H4 | CH3 | m.p.:132-134℃ |
I.131 | H | CH3 | 2-Cl-C6H4 | C2H5 | m.p.:104-108℃ |
I.132 | H | CH3 | 2-Cl-C6H4 | n-C3H7 | m.p.:63-66℃ |
I.133 | H | CH3 | 3-CH3-异噁唑-5-基 | CH3 | 油;IR(膜):2941,1728,1438,1220,1201,1070,1039,1019,959,897 |
I.134 | H | CH3 | 3-CH3-异噁唑-5-基 | C2H5 | 油;IR(膜):2941,1728,1438,1322,1220,1069,1038,1020,988,958 |
I.135 | H | CH3 | 3-CH3-异噁唑-5-基 | n-C3H7 | 油;IR(膜):2968,2940,1728,1438,1322,1220,1070,1047,1019,959 |
I.136 | H | CH3 | 3-CH3-异噁唑-5-基 | i-C3H7 | 油;IR(膜):2975,2935,1728,1438,1371,1324,1220,1119,1070,1049,1018,960 |
I.137 | H | CH3 | 3-CH3-异噁唑-5-基 | n-C4H9 | 油;IR(膜):2957,2939,1728,1438,1322,1220,1070,1020,985,958 |
I.138 | H | CH3 | 3-CH3-异噁唑-5-基 | n-C6H13 | 油;IR(膜):2936,1728,1437,1369,1321,1220,1201,1070,1019,958 |
I.139 | H | CH3 | 3-CH3-异噁唑-5-基 | 丙-1-烯-3-基 | 油;IR(膜):2940,1727,1438,1220,1201,1069,1048,1019,958,914,898 |
I.140 | H | CH3 | 3-CH3-异噁唑-5-基 | (E)-1-氯-丙-1-烯-3-基 | 油;IR(膜):2940,1728,1438,1220,1201,1070,1048,1018,988,957,898 |
I.141 | 3-Cl | CH3 | CH3 | CH3 | m.p.:105-107℃ |
I.142 | 3-Cl | CH3 | C6H5 | CH3 | m.p.:120-123℃ |
I.143 | 3-Cl | CH3 | C6H5 | C2H5 | m.p.:113-115℃ |
I.144 | H | SCH3 | CH3 | CH3 | 油;IR(膜):2930,1737,1432,1302,1221,1063,1048,1012,984,952,873 |
No. | R2 m | R3 | R4 | R5 | 数据 |
I.145 | H | SCH3 | CH3 | C2H5 | 油;IR(膜):2938,1728,1437,1220,1070,1047,1019,987,959,883 |
I.146 | H | SCH3 | CH3 | n-C3H7 | 油;IR(膜):2938,1728,1437,1321,1220,1070,1047,1018,989,958 |
I.147 | H | SCH3 | CH3 | i-C3H7 | 油;IR(膜):2956,2938,1728,1436,1220,1070,1040,1018,987,959 |
I.148 | H | SCH3 | CH3 | n-C6H13 | 油;IR(膜):2933,1729,1436,1321,1219,1070,1047,1018,989,958 |
I.149 | H | SCH3 | CH3 | 丙-1-烯-3-基 | 油;IR(膜):2930,1728,1436,1320,1219,1200,1069,1046,1017,990,958 |
I.150 | H | SCH3 | CH3 | 3-CF3-C6H4-CH2- | 油;IR(膜):2930,1729,1330,1220,1201,1166,1124,1072,1017,987,958 |
I.151 | H | CH3 | 3-吡啶基 | CH3 | 油;IR(膜):2935,1728,1438,1220,1201,1070,1042,1019,958,896,875 |
I.152 | H | CH3 | 3-吡啶基 | C2H5 | 油;IR(膜):2935,1728,1438,1322,1220,1202,1069,1044,1019,982,958 |
I.153 | H | CH3 | 3-吡啶基 | n-C3H7 | 油;IR(膜):2966,2939,1728,1437,1220,1070,1045,1020,984,958 |
I.154 | H | CH3 | 3-吡啶基 | i-C3H7 | 油;IR(膜):2965,1728,1371,1324,1220,1121,1070,1048,1021,977,960 |
I.155 | H | CH3 | 3-吡啶基 | n-C4H9 | 油;IR(膜):2957,2938,1728,1437,1219,1201,1071,1020,979,959 |
No. | R2 m | R3 | R4 | R5 | 数据 |
I.156 | H | CH3 | 3-吡啶基 | 丙-1-烯-3-基 | 油;IR(膜):2940,1728,1322,1220,1202,1070,1020,958 |
I.157 | H | CH3 | 3-吡啶基 | (E)-1-氯-丙-1-烯-3-基 | 油;IR(膜):2940,1728,1437,1322,1220,1202,1070,1049,1020,985,958 |
No. | R2 m | R3 | R4 | R5 | 数据 |
II.8 | H | CH3 | C6H5 | t-C4H9 | 油;IR(膜):768,971,1111,1130,1190,1256,1284,1346,1634,1710,2980 |
II.9 | H | CH3 | C6H5 | n-C6H13 | 油;IR(膜):1003,1030,1058,1111,1129,1255,1283,1634,1710,2933 |
II.10 | H | CH3 | C6H5 | 3-甲基-丁-2-烯-1-基 | 油;IR(膜):768,997,1111,1129,1255,1283,1435,1444,1630,1709,2930 |
II.11 | H | CH3 | C6H5 | 炔丙基 | 油;IR(膜):769,1006,1029,1058,1112,1130,1256,1285,1633,1708,2100,2940,3270 |
II.12 | H | CH3 | 4-Cl-C6H4 | CH3 | m.p.:109-113℃ |
II.13 | H | CH3 | 4-Cl-C6H4 | C2H5 | 油;IR(膜):1012,1036,1056,1091,1111,1130,1256,1284,1634,1710,2940 |
II.14 | H | CH3 | 4-Cl-C6H4 | n-C3H7 | 油;IR(膜):991,1012,1058,1092,1110,1129,1255,1284,1634,1710,2930,2960 |
II.15 | H | CH3 | 4-Cl-C6H4 | i-C3H7 | 油;IR(膜):998,1091,1111,1130,1255,1284,1435,1491,1634,1710,2930 |
II.16 | H | CH3 | 4-Cl-C6H4 | n-C4H9 | 油;IR(膜):977,1012,1091,1111,1129,1255,1284,1491,1634,1710,2930,2950 |
II.17 | H | CH3 | 4-Cl-C6H4 | t-C4H9 | 油;IR(膜):972,1111,1130,1189,1256,1284,1365,1490,1635,1711,2940,2970 |
II.18 | H | CH3 | 4-Cl-C6H4 | n-C6H13 | 油;IR(膜):1012,1058,1091,1111,1130,1256,1284,1635,1711,2933 |
II.19 | H | CH3 | 4-Cl-C6H4 | 炔丙基 | 油;IR(膜):1006,1028,1058,1092,1111,1130,1256,1285,1634,1708,2110,2940,3270 |
No. | R2 m | R3 | R4 | R5 | 数据 |
II.20 | H | CH3 | 4-F-C6H4 | CH3 | m.p.:113-118℃ |
II.21 | H | CH3 | 4-F-C6H4 | C2H5 | 油;IR(膜):1036,1056,1112,1130,1225,1256,1284,1509,1635,1710,2930,2970 |
II.22 | H | CH3 | 4-F-C6H4 | n-C3H7 | 油;IR(膜):992,1064,1112,1130,1225,1256,1284,1509,1635,1710,2940,2960 |
II.23 | H | CH3 | 4-F-C6H4 | i-C3H7 | 油;IR(膜):975,1113,1129,1158,1225,1256,1284,1508,1634,1710,2930,2960 |
II.24 | H | CH3 | 4-F-C6H4 | n-C4H9 | 油:IR(膜):1000,1013,1112,1130,1225,1256,1284,1508,1635,1710,2920,2940 |
II.25 | H | CH3 | 4-F-C6H4 | 2-甲基-丙-1-基 | 油;IR(膜):1003,1029,1111,1130,1225,1256,1284,1508,1635,1710,2950 |
II.26 | H | CH3 | 4-F-C6H4 | t-C4H9 | 油;IR(膜):973,1111,1130,1189,1225,1256,1365,1508,1635,1710,2940,2970 |
II.27 | H | CH3 | 4-F-C6H4 | n-C6H13 | 油;IR(膜):1002,1111,1130,1226,1256,1284,1508,1635,1711,2933 |
II.28 | H | CH3 | 4-F-C6H4 | 3-Cl-丙-2-烯-1-基 | 油;IR(膜):1012,1058,1111,1130,1226,1256,1285,1509,1635,1709,2940 |
II.29 | H | CH3 | 4-F-C6H4 | 炔丙基 | 油;IR(膜):1006,1028,1112,1130,1226,1256,1285,1509,1630,1708,2110,2940,3280 |
II.30 | H | CH3 | 4-OCH3-C6H4 | CH3 | 油;IR(膜):1035,1057,1111,1129,1174,1253,1512,1608,1633,1708,2930 |
II.31 | H | CH3 | 4-OCH3-C6H4 | C2H5 | 油;IR(膜):1036,1058,1112,1130,1176,1254,1286,1512,1634,1709,2930,2960 |
No. | R2 m | R3 | R4 | R5 | 数据 |
II.32 | H | CH3 | 4-OCH3-C6H4 | n-C3H7 | 油;IR(膜):990,1036,1111,1129,1176,1254,1285,1512,1634,1709,2930,2960 |
II.33 | H | CH3 | 4-OCH3-C6H4 | i-C3H7 | 油;IR(膜):972,1032,1113,1129,1174,1253,1286,1512,1634,1709,2930,2960 |
II.34 | H | CH3 | 4-OCH3-C6H4 | n-C4H9 | 油;IR(膜):838,998,1025,1111,1132,1176,1254,1262,1634,1711,2920,2940 |
II.35 | H | CH3 | 4-OCH3-C6H4 | t-C4H9 | 油;IR(膜):960,1034,1111,1129,1175,1190,1252,1511,1633,1709,2960 |
II.36 | H | CH3 | 4-OCH3-C6H4 | 2-甲基-丙-1-基 | 油;IR(膜):1004,1031,1111,1129,1175,1253,1512,1607,1634,1709,2950 |
II.37 | H | CH3 | 4-OCH3-C6H4 | 炔丙基 | 油;IR(膜):1006,1030,1112,1130,1175,1255,1512,1608,1633,1707,2110,2930,3270 |
II.38 | H | CH3 | 4-Cl-C6H4 | 3-甲基-丁-2-烯-1-基 | 油;IR(膜):996,1091,1111,1130,1256,1284,1435,1491,1634,1710,2930 |
II.39 | H | CH3 | CH3 | CH3 | 油;IR(膜):2930,1710,1635,1284,1255,1129,1110,1057,1032,903,888 |
II.40 | H | CH3 | CH3 | C2H5 | 油;IR(膜):2935,1710,1635,1366,1284,1256,1130,1111,1044,919,891 |
II.41 | H | CH3 | CH3 | n-C3H7 | 油;IR(膜):2930,1711,1635,1284,1256,1129,1110,1044,1019,990,926 |
II.42 | H | CH3 | CH3 | i-C3H7 | 油;IR(膜):2965,1711,1635,1366,1284,1256,1130,1113,986,914,894 |
II.43 | H | CH3 | CH3 | n-C4H9 | 油;IR(膜):2957,2936,1711,1635,1365,1284,1256,1130,1111,1029 |
No. | R2 m | R3 | R4 | R5 | 数据 |
II.44 | H | CH3 | CH3 | i-C4H9 | 油;IR(膜):2956,1711,1635,1366,1284,1256,1130,1111,1032,926 |
II.45 | H | CH3 | CH3 | t-C4H9 | 油;IR(膜):2965,1711,1635,1365,1256,1192,1129,1110,984,930,894 |
II.46 | H | CH3 | CH3 | n-C6H13 | 油;IR(film):2934,1712,1635,1365,1284,1256,1130,1111,1058,1020 |
II.47 | H | CH3 | CH3 | (E)-1-氯丙-1-烯-3-基 | 油;IR(膜):2940,1709,1634,1366,1285,1255,1130,1110,1019,988,893 |
II.48 | H | CH3 | CH3 | 丙-1-烯-3-基 | 油;IR(膜):2940,1710,1634,1366,1284,1256,1130,1110,1024,1001,919 |
II.49 | H | CH3 | CH3 | 丙炔-3-基 | 油;IR(膜):3269,2940,2110,1702,1624,1254,1245,1128,1110,1025,995,896 |
II.50 | H | CH3 | CH3 | 3,7-二甲基-2,6-辛二烯-1-基 | 油;IR(膜):2932,1712,1635,1436,1365,1255,1130,1111,1002,895 |
II.51 | H | CH3 | CH3 | 3-CF3-C6H4 | 油;IR(膜):2940,1710,1448,1328,1281,1255,1168,1127,1062,927 |
II.52 | H | CH3 | CH3 | 3-CF3-C6H4-CH2 | 油;IR(膜):2940,1710,1635,1330,1256,1202,1192,1166,1128,1074,1018 |
II.53 | H | CH3 | CH3 | 3-CF3-C6H4-CH(CH3) | 油;IR(f膜):2925,1710,1635,1329,1271,1257,1204,1166,1128,1073,892 |
II.54 | H | CH3 | CH3 | C6H5-CH2-CH2-O-CH2-CH2 | 油;IR(膜):2935,1710,1634,1365,1284,1256,1129,1112,1057,1038,1002 |
II.55 | H | CH3 | CH3 | 6-(4’-氯苯基)己-1-基 | 油;IR(膜):2935,1710,1635,1492,1284,1255,1130,1111,1029,1015 |
No. | R2 m | R3 | R4 | R5 | 数据 |
II.56 | H | CH3 | CH3 | 4-Cl-C6H4-CH2-CH2-O-CH2-CH2 | 油;IR(膜):2935,1709,1635,1493,1284,1256,1129,1112,1057,1038,1015 |
II.57 | H | CH3 | CH3 | 6-(4’-氟苯基)己-1-基 | 油;IR(膜):2934,1710,1635,1510,1256,1220,1130,1110,1029,1003 |
II.58 | 3-Cl | CH3 | CH3 | CH3 | m.p.:125-127℃ |
II.59 | 3-Cl | CH3 | C6H5 | CH3 | m.p.:171-173℃ |
II.60 | 3-Cl | CH3 | C6H5 | C2H5 | m.p.:128-131℃ |
No. | R2 m | R3 | R4 | R5 | 数据 |
III.18 | H | CH3 | CH3 | n-C6H13 | 油;IR(膜):2954,2932,1720,1434,1365,1252,1036,984,921,897 |
III.19 | H | CH3 | CH3 | (E)-1-氯-丙-1-烯-3-基 | 油;IR(膜):2940,2920,1717,1435,1366,1253,1208,1020,983,934,894,761 |
III.20 | H | CH3 | CH3 | 丙-1-烯-3-基 | 油;IR(膜):2950,1719,1435,1366,1253,1208,1026,919,890,761 |
III.21 | H | CH3 | CH3 | 丙炔-3-基 | 油;IR(膜):3290,2950,2930,2125,1717,1435,1366,1254,1208,1033,1009,881 |
III.22 | H | CH3 | CH3 | 3,7-二甲基-2,6-辛二烯-1-基 | 油;IR(膜):2967,2928,1720,1435,1376,1365,1252,1015,888 |
III.23 | H | CH3 | CH3 | 3-CF3-C6H4 | 油;IR(膜):2950,1717,1449,1328,1281,1253,1210,1169,1126,927,900 |
III.24 | H | CH3 | CH3 | 3-CF3-C6H4-CH2 | 油;IR(膜):2940,2920,1717,1366,1330,1254,1202,1166,1127,1074,1034,884 |
III.25 | H | CH3 | CH3 | 3-CF3-C6H4-CH(CH3) | 油;IR(膜):2980,1717,1329,1269,1255,1204,1166,1126,1073,1014,704 |
III.26 | H | CH3 | CH3 | C6H5-CH2-CH2-O-CH2-CH2 | 油;IR(膜):2940,1717,1435,1365,1253,1121,1036,983,893,750,700 |
III.27 | H | CH3 | CH3 | 6-(4’-氯苯基)己-1-基 | 油;IR(膜):2933,2857,1717,1492,1365,1253,1092,1034,1015,987 |
III.28 | H | CH3 | CH3 | 4-Cl-C6H4-CH2-CH2-O-CH2-CH2 | 油;IR(膜):2940,2920,1717,1493,1365,1253,1122,1091,1037,1016,983,894 |
III.29 | H | CH3 | CH3 | 6-(4’-氟苯基)己-1-基 | 油;IR(膜):2933,2858,1717,1510,1365,1254,1221,1157,1034,893 |
III.30 | 3-Cl | CH3 | CH3 | CH3 | m.p.:60-61℃ |
No. | R2 m | R3 | R4 | R5 | 数据 |
III.31 | 3-Cl | CH3 | C6H5 | CH3 | 油;IR(膜):1037,1256,1435,1444,1718,2930 |
III.32 | 3-Cl | CH3 | C6H5 | C2H5 | 油;IR(膜):1038,1256,1435,1443,1718,2940,2970 |
抗有害真菌作用实施例:
用以下的实验可以证明通式I的化合物的杀真菌活性:
将活性化合物在70%重量的环己酮、20%重量的NekanilRLN(LutensolR AP6,具有乳化和分散活性的增湿剂,基于乙氧化烷基酚)和10%重量的EmulphorR EL(EulanR EL,基于乙氧基化脂肪醇的乳化剂)的混合物中制备成20%浓度的乳剂,并用水稀释到所需的相应浓度。
1.禾田粉菌(Erysiphe graminis Var.tritici)
首先用活性化合物的含水制剂(含250ppm)处理小麦苗(Kazlervariety)叶子。约24小时后,将该植物用小麦粉霉孢子(Erysiphe graminisvar.tritici)喷撒。然后将如此处理的植物在20-22℃以及75-80%的相对湿度下培养7天。然后测定真菌生长的程度。
在这个试验中,用本发明化合物处理的植物有15%或更少被侵害,用已知活性化合物(EP-A 463488,表3,No.195化合物)处理的植物有40%被侵害,未处理的植物有70%被侵害。
在首先将植物感染并培养、然后再用活性化合物处理的相应试验中(Kanzler variety,施用率为63ppm),本发明化合物处理的植物有5%或更少被侵害,用已知活性化合物(EP-A 463488,表3,No.195化合物)处理的植物有25%被侵害,未处理的植物有60%被侵害。
抗动物害虫活性的实施例
通过下面试验可显示通式I化合物的杀虫活性:
将活性化合物
a)在丙酮中制备成0.1%浓度的溶液或
b)在70%重量环己醇、20%重量NekanilR LN(LutensolR AP6,具有乳化和分散活性的增湿剂,基于乙氧化烷基酚)和10%重量的EmulphorREL(基于乙氧化脂肪醇的乳化剂)的混合物中制备成10%浓度的乳剂,并在a)中用丙酮、在b)中用水相应地稀释到所需的浓度。
试验结束后,测定各种情况下与未处理的对照试验相比,试验化合物仍可导致80-100%抑制或死亡率的最低浓度(作用极限或最低浓度)。
蚕豆蚜,接触作用
用活性化合物含水制剂处理严重感染的短豆(Vicia faba)。测定24小时后的死亡率。
在这个实验中,本发明化合物I.67,I.68,I.71,I.72,I.73,I.98,I.105,I.106,I.109,I.110,II.02,II.05,II.09,II.12,II.13,II.14,II.16,II.24,II.102,III.01,III.02和III.10显示400ppm或更低的作用极限浓度。
黑尾叶蝉(green rice leaf hopeer),接触作用
用活性化合物含水制剂处理圆形滤器,然后放入5只成年蝗虫(leathopper)。24h后测定死亡率。
在这个试验中,本发明化合物I.68,I.81,I.82,I.83,I.96,II.09,II.12,II.13,II.14,II.19,II.27和III.02显示0.4mg或更低的作用极限用量。
斜纹夜蛾(Egyptian cotton leaf worm),接触作用
用活性化合物含水制剂处理滤器,然后放入5只毛虫。4小时后先作一次测定。如果有至少一只毛虫还活着,加入饲料混合物。24小时后测定死亡率。
这个试验中,本发明化合物I.82,I.95,I.96,I.105,I.106,I.112,II.03,II.09,II.11,II.12,II.13,II.14,II.16,iI.18,II.19,II.20,II.22,II.23,II.24,II.25,II.27,II.28,II.29和III.10显示0.4mg成更低的作用极限用量。
红棉叶螨(common red spider mite),接触作用
用活性化合物含水制剂处理具有连续的第二对叶片的罐装矮豆。24小时后,用严重感染的叶片感染该植物。在温室中测定12天后的侵害程度。
在这个试验中,化合物I.07,I.95,I.105,I.106,I.107,I.109,I.110,II.03,II.04,II.06,II.07,II.09,II.10,II.16,II.18,II.19,II.20,II.22,II.24,II.25,II.26,II.27,II.28和II.29显示400ppm或更低的作用极限浓度。
Claims (14)
1.式I表示的苯乙酸衍生物及其盐其中的取代基和符号定义如下:X 为NOCH3,CHOCH3,CHCH3和CHCH2CH3;R1 为氢和C1-C4-烷基;R2 为氰基,硝基,三氟甲基,卤素,C1-C4-烷基和C1-C4-烷
氧基;m 为0,1或2,如果m为2,R2可为不同的基团;R3 为氢,氰基,硝基,羟基,氨基,卤素,C1-C4-烷基,C1-C4
-卤代烷基,C1-C4-烷氧基,C1-C4-卤代烷氧基,C1-C4
-烷硫基,C1-C4-烷氨基或双-C1-C4-烷基氨基;R4 为氢,氰基,硝基,羟基,氨基,卤素,C1-C6-烷基,C1-C6
-烷氧基,C1-C6-烷硫基,C1-C6-烷氨基,双-C1-C6
-烷基氨基,C2-C6-链烯基,C2-C6-链烯氧基,C2-C6
-链烯硫基,C2-C6-链烯氨基,N-C2-C6-链烯基-N-
C1-C6-烷基氨基,C2-C6-链炔基,C2-C6-链炔氧基,
C2-C6-链炔硫基,C2-C6-链炔氨基,N-C2-C6-链炔
基-N-C1-C6-烷基氨基,这些基团中的烃基部分可被部分或
完全卤代或带有一到三个下列基团:氰基,硝基,羟基,巯基,氨
基,羧基,氨羰基,氨硫代羰基,卤素,C1-C6-烷氨基羰基,
双-C1-C6-烷基氨基羰基,C1-C6-烷氨基硫代羰基,双-
C1-C6-烷基氨基硫代羰基,C1-C6-烷基磺酰基,C1-C6
烷基亚磺酰基,C1-C6-烷氧基,C1-C6-卤代烷氧基,C1-
C6-烷氧羰基,C1-C6-烷硫基,C1-C6-烷氨基,双-C1-C6-烷基氨基,C2-C6链烯氧基,C3-C6-环烷基,C3-C6-环烷氧基,杂环基,杂环氧基,芳基,芳氧基,芳基-C1-C4-烷氧基,芳硫基,芳基-C1-C4-烷硫基,杂芳基,杂芳氧基,杂芳基-C1-C4-烷氧基,杂芳硫基,杂芳基-C1-C4-烷硫基,这些环状基团环基部分又可被部分或完全卤代和/或带有一到三个下列基团:氰基,硝基,羟基,巯基,氨基,羧基,氨羰基,氨硫代羰基,C1-C6烷基,C1-C6-卤代烷基,C1-C6-烷基磺酰基,C1-C6-烷基亚磺酰基,C3-C6-环烷基,C1-C6-烷氧基,C1-C6-卤代烷氧基,C1-C6-烷氧羰基,C1-C6-烷硫基,C1-C6-烷氨基,双-C1-C6-烷基氨基,C1-C6-烷氨基羰基,双-C1-C6-烷基氨基羰基,C1-C6-烷氨基硫代羰基,双-C1-C6-烷基氨基硫代羰基,C2-C6-链烯基,C2-C6-链烯氧基,苄基,苄氧基,芳基,芳氧基,芳硫基,杂芳基,杂芳氧基,杂芳硫基,和C(=NOR6)-An-R7;C3-C6-环烷基,C3-C6-环烷氧基,C3-C6-环烷硫基,C3-C6-环烷氨基,N-C3-C6-环烷基-N-C1-C6-烷基氨基,C3-C6-环烯基,C3-C6-环烯氧基,C3-C6-环烯硫基,C3-C6-环烯氨基,N-C3-C6-环烯基-N-C1-C6-烷基氨基,杂环基,杂环氧基,杂环硫基,杂环氨基,N-杂环基-N-C1-C6-烷基氨基,芳基,芳氧基,芳硫基,芳氨基,N-芳基-N-C1-C6-烷基氨基,杂芳基,杂芳氧基,杂芳硫基,杂芳氨基,N-杂芳基-N-C1-C6-烷基氨基,这些环状基团可被部分或完全卤代或带有一到三个下列基团:氰基,硝基,羟基,巯基,氨基,羧基,氨羰基,氨硫代羰基,卤素,C1-C6-烷基,C1-C6-卤代烷基,C1-C6-烷基磺酰基,C1-C6-烷基亚磺酰基,C3-C6-环烷基,C1-C6-烷氧基,C1-C6-卤代烷氧基,C1-C6-烷氧羰基,C1-C6-烷硫基,C1-C6-烷氨基,双-C1-C6-烷基氨基,C1-C6-烷氨基羰基,双-C1-C6-烷基氨基羰基,C1-C6-烷氨基硫代羰基,双-C1-C6-烷基氨基硫代羰基,C2-C6-链烯基,C2-C6-链
烯氧基,苄基,苄氧基,芳基,芳氧基,杂芳基和杂芳氧基;R5 为氢,
C1-C10-烷基,C3-C6-环烷基,C2-C10-链烯基,C2-
C10-链炔基,C1-C10-烷羰基,C2-C10-链烯羰基,C3-
C10-链炔羰基或C1-C10-烷基磺酰基,这些基团可被部分或完
全卤代或带有一到三个下列基团:氰基,硝基,羟基,巯基,氨基,
羧基,氨羰基,氨基硫代羰基,卤素,C1-C6-烷基,C1-C6
-卤代烷基,C1-C6-烷基磺酰基,C1-C6-烷基亚磺酰基,
C1-C6-烷氧基,C1-C6-卤代烷氧基,C1-C6-烷氧羰基,
C1-C6-烷硫基,C1-C6-烷氨基,双-C1-C6-烷基氨基,
C1-C6-烷氨基羰基,双-C1-C6-烷基氨基羰基,C1-C6
-烷氨基硫代羰基,双-C1-C6-烷基氨基硫代羰基,C2-C6
-链烯基,C2-C6-链烯氧基,C3-C6-环烷基,C3-C6-
环烷氧基,杂环基,杂环氧基,苄基,苄氧基,芳基,芳氧基,芳
硫基,杂芳基,杂芳氧基和杂芳硫基,这些环状基团又可被部分或
完全卤代或带有一到三个下列基团:氰基,硝基,羟基,巯基,氨
基,羧基,氨羰基,氨基硫代羰基,卤素,C1-C6-烷基,C1
-C6-卤代烷基,C1-C6-烷基磺酰基,C1-C6-烷基亚磺酰
基,C3-C6-环烷基,C1-C6-烷氧基,C1-C6-卤代烷氧
基,C1-C6-烷氧羰基,C1-C6-烷硫基,C1-C6-烷氨基,
双-C1-C6-烷基氨基,C1-C6-烷氨基羰基,双-C1-C6
-烷基氨基羰基,C1-C6-烷氨基硫代羰基,双-C1-C6-烷
基氨基硫代羰基,C2-C6-链烯基,C2-C6-链烯氧基,苄基,
苄氧基,芳基,芳氧基,芳硫基,杂芳基,杂芳氧基,杂芳硫基,
或C(=NOR6)-An-R7;
芳基,芳羰基,芳基磺酰基,杂芳基,杂芳基羰基或杂芳基磺酰基,
这些基团可被部分或完全卤代或带有一到三个下列基团:氰基,硝
基,羟基,巯基,氨基,羧基,氨基羰基,氨基硫羰基,卤素,C1
-C6-烷基,C1-C6-卤代烷基,C1-C6-烷基羰基,C1-
C6-烷基磺酰基,C1-C6-烷基亚磺酰基,C3-C6-环烷基,
C1-C6-烷氧基,C1-C6-卤代烷氧基,C1-C6-烷氧羰基,
C1-C6-烷硫基,C1-C6-烷氨基,双-C1-C6-烷基氨基,
C1-C6-烷氨基羰基,双-C1-C6-烷基氨基羰基,C1-C6-
烷氨基硫代羰基,双-C1-C6-烷基氨基硫代羰基,C2-C6链
烯基,C2-C6-链烯氧基,苄基,苄氧基,芳基,芳氧基,杂芳
基,杂芳氧基或C(=NOR6)-An-R7;其中A 为氧、硫或氮,其中氮带有氢或C1-C6烷基;n 为0或1;R6 为氢或C1-C6-烷基,以及R7 为氢或C1-C6-烷基,其中,当R3为氢且R5为烷基时,X不是CHOCH3。
2.根据权利要求1的式I化合物,其中R3、R4和R5定义如下:R3 为氢、羟基、环丙基、卤素、C1-C4-烷基、C1-C4-烷氧基
或C1-C4-烷硫基,R4 为氢,羟基,卤素,环丙基,环己基,C1-C4-烷基,C1-C4
-烷氧基,C1-C4-烷硫基,
芳基或杂芳基,这些基团可被部分或完全卤代或带有一到三个选自
下列的基团:氰基,硝基,羟基,巯基,氨基,羧基,氨羰基,氨
基硫代羰基,卤素,C1-C6-烷基,C1-C6-卤代烷基,C1-
C6-烷基磺酰基,C1-C6-烷基亚磺酰基,C3-C6-环烷基,
C1-C6-烷氧基,C1-C6-卤代烷氧基,C1-C6-烷氧羰基,
C1-C6-烷硫基,C1-C6-烷氨基,双-C1-C6-烷基氨基,
C1-C6-烷氨基羰基,双-C1-C6-烷基氨羰基,C1-C6-烷
氨基硫代羰基,双-C1-C6-烷基氨基巯代羰基,C2-C6-链烯
基,C2-C6-链烯氧基,苄基,苄氧芳基,芳氧基,杂芳基和杂
芳氧基;R5 为氢,
C1-C10-烷基,C3-C6-环烷基,C2-C10-链烯基,C2-
C10-链炔基,C1-C10-烷羰基,C2-C10-链烯羰基,C3-
C10-链炔羰基或C1-C10-烷基磺酰基,这些基团可被部分或完全
卤代或带有一到三个选自下列的基团:氰基,硝基,羟基,巯基,
氨基,羧基,氨羰基,氨基硫代羰基,卤素,C1-C6-烷基,C1
-C6-卤代烷基,C1-C6-烷基磺酰基,C1-C6-烷基亚磺酰
基,C3-C6-环烷基,C1-C6-烷氧基,C1-C6-卤代烷基,
C1-C6-烷氧羰基,C1-C6-烷硫基,C1-C6-烷氨基,双-
C1-C6-烷基氨基,C1-C6-烷基氨羰基,双-C1-C6-烷基
氨羰基,C1-C6-烷氨基硫代羰基,双-C1-C6-烷基氨基巯代
羰基,C2-C6-链烯基,C2-C6-链烯氧基,苄基,苄氧基,芳
基,芳氧基,芳硫基,杂芳基,杂芳氧基和杂芳硫基,这些芳基和
杂芳基又可被部分或完全卤化和/或带有一到三个下列基团:氰基,
硝基,羟基,巯基,氨基,羧基,氨羰基,氨基硫代羰基,卤素,
C1-C6-烷基,C1-C6-卤代烷基,C1-C6-烷基磺酰基,C1
-C6-烷基亚磺酰基,C3-C6-环烷基,C1-C6-烷氧基,C1
-C6-卤代烷氧基,C1-C6-烷氧羰基,C1-C6-烷硫基,C1
-C6-烷氨基,双-C1-C6-烷基氨基,C1-C6-烷氨基羰基,
双-C1-C6-烷基氨羰基,C1-C6-烷氨基硫代羰基,双-C1
-C6-烷基氨基硫代羰基,C2-C6-链烯基,C2-C6-链烯氧
基,苄基,苄氧基,芳基,芳氧基,芳硫基,杂芳基,杂芳氧基,
杂芳硫基或C(=NO R6)-An-R7,
其中,当R3为氢且R5为烷基时,X不是CHOCH3。
3.根据权利要求1的式I化合物,其中m为0。
4.根据权利要求1的式I化合物,其中R1为甲基。
5.制备其中R3不为卤素的权利要求1的式I化合物的方法,其中包括,以本质已知的方式使式II苄基衍生物。
其中L1为可被亲核取代的离去基团,
与式III的羟基亚胺反应
R5OH=C(R4)-C(R3)=NOH III。
7.制备其中R3不为卤素的权利要求1的式I化合物的方法,其中包括,以本质已知的方式使如权利要求1中的式II苄基衍生物与式VII羰基羟基亚胺
O=C(R4)-C(R3)=NOH VII
反应,得到式VIII化合物
然后使VIII
a)首先与羟胺或其盐反应,然后与如权利要求6的式VI(R5-L2)化合物反应,或者
b)与式IXa或IXb的羟胺或羟基铵盐反应,
R5-ONH2 R5-ONH3 )Q⊕
IXa Ixb
其中Q⊕为酸根离子
得到I。
8.一种抗动物害虫或有害真菌的组合物,其中含有常规添加剂和有效量的权利要求1的式I化合物。
9.根据权利要求8的组合物,其中用于控制昆虫、珠形纲或线虫类动物害虫。
10.一种控制有害真菌的方法,其中包括,用有效量的权利要求1的式I化合物处理有害真菌、它们生存的环境或植物、表面、物质或空间,使它们不受有害真菌的侵害。
11.一种控制动物害虫的方法,其中包括,用有效量的权利要求1的式I化合物处理害虫、它们生存的环境或植物、表面、物质或空间,使它们不受害虫的侵害,
其中,式I中的取代基和符号的意义如下:X 为NOCH3,CHOCH3,CHCH3和CHCH2CH3;R1 为氢和C1-C4-烷基;R2 为氰基,硝基,三氟甲基,卤素,C1-C4-烷基和C1-C4-烷
氧基;m 为0,1或2,如果m为2,R2可为不同的基团;R3 为氢,氰基,硝基,羟基,氨基,卤素,C1-C4-烷基,C1-C4
-卤代烷基,C1-C4-烷氧基,C1-C4-卤代烷氧基,C1-C4
-烷硫基,C1-C4-烷氨基或双-C1-C4-烷基氨基;R4 为氢,氰基,硝基,羟基,氨基,卤素,C1-C6-烷基,C1-C6
-烷氧基,C1-C6-烷硫基,C1-C6-烷氨基,双-C1-C6
-烷基氨基,C2-C6-链烯基,C2-C6-链烯氧基,C2-C6
-链烯硫基,C2-C6-链烯氨基,N-C2-C6-链烯基-N-
C1-C6-烷基氨基,C2-C6-链炔基,C2-C6-链炔氧基,
C2-C6-链炔硫基,C2-C6-链炔氨基,N-C2-C6-链炔
基-N-C1-C6-烷基氨基,这些基团中的烃基部分可被部分或
完全卤代或带有一到三个下列基团:氰基,硝基,羟基,巯基,氨
基,羧基,氨羰基,氨硫代羰基,卤素,C1-C6-烷氨基羰基,
双-C1-C6-烷基氨基羰基,C1-C6-烷氨基硫代羰基,双-
C1-C6-烷基氨基硫代羰基,C1-C6-烷基磺酰基,C1-C6
烷基亚磺酰基,C1-C6-烷氧基,C1-C6-卤代烷氧基,C1-
C6-烷氧羰基,C1-C6-烷硫基,C1-C6-烷氨基,双-C1
-C6-烷基氨基,C2-C6链烯氧基,C3-C6-环烷基,C3-
C6-环烷氧基,杂环基,杂环氧基,芳基,芳氧基,芳基-C1-
C4-烷氧基,芳硫基,芳基-C1-C4-烷硫基,杂芳基,杂芳氧
基,杂芳基-C1-C4-烷氧基,杂芳硫基,杂芳基-C1-C4-
烷硫基,这些环状基团环基部分又可被部分或完全卤代和/或带有一
到三个下列基团:氰基,硝基,羟基,巯基,氨基,羧基,氨羰基,
氨硫代羰基,C1-C6烷基,C1-C6-卤代烷基,C1-C6-烷
基磺酰基,C1-C6-烷基亚磺酰基,C3-C6-环烷基,C1-C6
-烷氧基,C1-C6-卤代烷氧基,C1-C6-烷氧羰基,C1-C6
-烷硫基,C1-C6-烷氨基,双-C1-C6-烷基氨基,C1-C6
-烷氨基羰基,双-C1-C6-烷基氨基羰基,C1-C6-烷氨基
硫代羰基,双-C1-C6-烷基氨基硫代羰基,C2-C6-链烯基,
C2-C6-链烯氧基,苄基,苄氧基,芳基,芳氧基,芳硫基,杂
芳基,杂芳氧基,杂芳硫基,和C(=NOR6)-An-R7;
C3-C6-环烷基,C3-C6-环烷氧基,C3-C6-环烷硫基,
C3-C6-环烷氨基,N-C3-C6-环烷基-N-C1-C6-烷
基氨基,C3-C6-环烯基,C3-C6-环烯氧基,C3-C6-环
烯硫基,C3-C6-环烯氨基,N-C3-C6-环烯基-N-C1
-C6-烷基氨基,杂环基,杂环氧基,杂环硫基,杂环氨基,N
-杂环基-N-C1-C6-烷基氨基,芳基,芳氧基,芳硫基,芳
氨基,N-芳基-N-C1-C6-烷基氨基,杂芳基,杂芳氧基,
杂芳硫基,杂芳氨基,N-杂芳基-N-C1-C6-烷基氨基,这
些环状基团可被部分或完全卤代或带有一到三个下列基团:氰基,
硝基,羟基,巯基,氨基,羧基,氨羰基,氨硫代羰基,卤素,C1
-C6-烷基,C1-C6-卤代烷基,C1-C6-烷基磺酰基,C1
-C6-烷基亚磺酰基,C3-C6-环烷基,C1-C6-烷氧基,C1
-C6-卤代烷氧基,C1-C6-烷氧羰基,C1-C6-烷硫基,C1
-C6-烷氨基,双-C1-C6-烷基氨基,C1-C6-烷氨基羰基,
双-C1-C6-烷基氨基羰基,C1-C6-烷氨基硫代羰基,双-
C1-C6-烷基氨基硫代羰基,C2-C6-链烯基,C2-C6-链
烯氧基,苄基,苄氧基,芳基,芳氧基,杂芳基和杂芳氧基;R5 为氢,
C1-C10-烷基,C3-C6-环烷基,C2-C10-链烯基,C2-
C10-链炔基,C1-C10-烷羰基,C2-C10-链烯羰基,C3-
C10-链炔羰基或C1-C10-烷基磺酰基,这些基团可被部分或完
全卤代或带有一到三个下列基团:氰基,硝基,羟基,巯基,氨基,
羧基,氨羰基,氨基硫代羰基,卤素,C1-C6-烷基,C1-C6
-卤代烷基,C1-C6-烷基磺酰基,C1-C6-烷基亚磺酰基,
C1-C6-烷氧基,C1-C6-卤代烷氧基,C1-C6-烷氧羰基,
C1-C6-烷硫基,C1-C6-烷氨基,双-C1-C6-烷基氨基,
C1-C6-烷氨基羰基,双-C1-C6-烷基氨基羰基,C1-C6
-烷氨基硫代羰基,双-C1-C6-烷基氨基硫代羰基,C2-C6
-链烯基,C2-C6-链烯氧基,C3-C6-环烷基,C3-C6-
环烷氧基,杂环基,杂环氧基,苄基,苄氧基,芳基,芳氧基,芳
硫基,杂芳基,杂芳氧基和杂芳硫基,这些环状基团又可被部分或
完全卤代或带有一到三个下列基团:氰基,硝基,羟基,巯基,氨
基,羧基,氨羰基,氨基硫代羰基,卤素,C1-C6-烷基,C1
-C6-卤代烷基,C1-C6-烷基磺酰基,C1-C6-烷基亚磺酰
基,C3-C6-环烷基,C1-C6-烷氧基,C1-C6-卤代烷氧
基,C1-C6-烷氧羰基,C1-C6-烷硫基,C1-C6-烷氨基,
双-C1-C6-烷基氨基,C1-C6-烷氨基羰基,双-C1-C6
-烷基氨基羰基,C1-C6-烷氨基硫代羰基,双-C1-C6-烷
基氨基硫代羰基,C2-C6-链烯基,C2-C6-链烯氧基,苄基,
苄氧基,芳基,芳氧基,芳硫基,杂芳基,杂芳氧基,杂芳硫基,
或C(=NOR6)-An-R7;
芳基,芳羰基,芳基磺酰基,杂芳基,杂芳基羰基或杂芳基磺酰基,
这些基团可被部分或完全卤代或带有一到三个下列基团:氰基,硝
基,羟基,巯基,氨基,羧基,氨基羰基,氨基硫羰基,卤素,C1
-C6-烷基,C1-C6-卤代烷基,C1-C6-烷基羰基,C1-
C6-烷基磺酰基,C1-C6-烷基亚磺酰基,C3-C6-环烷基,
C1-C6-烷氧基,C1-C6-卤代烷氧基,C1-C6-烷氧羰基,
C1-C6-烷硫基,C1-C6-烷氨基,双-C1-C6-烷基氨基,
C1-C6-烷氨基羰基,双-C1-C6-烷基氨基羰基,C1-C6-
烷氨基硫代羰基,双-C1-C6-烷基氨基硫代羰基,C2-C6链
烯基,C2-C6-链烯氧基,苄基,苄氧基,芳基,芳氧基,杂芳
基,杂芳氧基或C(=NOR6)-An-R7;其中A 为氧、硫或氮,其中氮带有氢或C1-C6烷基;n 为0或1;R6 为氢或C1-C6-烷基,以及R7 为氢或C1-C6-烷基。
12.权利要求1的化合物I用于制备抗动物害虫和有害真菌的组合物的用途。
13.权利要求1的化合物I用于控制动物害虫和有害真菌的应用。
14.权利要求5中的式III所示羟基亚胺,其中,R3、R4和R5的意义同权利要求1中所述。
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Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104039144A (zh) * | 2011-11-30 | 2014-09-10 | 组合化学工业株式会社 | 乙二肟衍生物及有害生物防除剂 |
Families Citing this family (61)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU690190B2 (en) * | 1994-01-05 | 1998-04-23 | Bayer Aktiengesellschaft | Pesticides |
PL179077B1 (en) * | 1994-02-04 | 2000-07-31 | Basf Ag | Derivatives of phenyloacetic acid, method of and intermediate products for obtaining them and agents containing such derivatives |
CH689228A5 (de) * | 1994-10-07 | 1998-12-31 | Novartis Ag | Oximether, sowie diese enthaltende Pflanzenschutzmittel. |
DE69514120T2 (de) * | 1994-11-17 | 2000-08-10 | Novartis Ag, Basel | Derivate von o-benzyl-oxin-ether sowie deren verwendung als pestizide |
BR9604822A (pt) * | 1995-04-08 | 1998-06-09 | Basf Ag | Processo para a preparação de alfa-bisoximas em grande parte isomericamente puras |
CA2221757A1 (en) * | 1995-06-22 | 1997-01-09 | Novartis Ag | Pesticidal tris-oximino heterocyclic compounds |
ATE193011T1 (de) * | 1995-06-27 | 2000-06-15 | Novartis Ag | O-benzyloximether-derivate und ihre verwendung in pflanzenschutzmitteln |
JPH11508569A (ja) * | 1995-07-04 | 1999-07-27 | ノバルティス アクチェンゲゼルシャフト | トリアゾリン及びイソキサゾリンビス−オキシム誘導体並びに殺虫剤としてのその用途 |
AU713472B2 (en) * | 1995-07-27 | 1999-12-02 | Basf Aktiengesellschaft | Phenylacetic acid derivatives, processes and intermediates for their preparation, and compositions comprising them |
DE19528651A1 (de) * | 1995-08-04 | 1997-02-06 | Basf Ag | Hydroximsäurederivate, Verfahren zu ihrer Herstellung und sie enthaltende Mittel |
JPH11512446A (ja) * | 1995-09-18 | 1999-10-26 | ビーエーエスエフ アクチェンゲゼルシャフト | フェニル酢酸、その製造及びそれを含む組成物 |
AR004012A1 (es) | 1995-10-10 | 1998-09-30 | Basf Ag | Derivados de acido fenilacetico, procedimientos para su obtencion, su uso para preparar composiciones para combatir animales u hongos nocivos, lascomposiciones asi obtenidas y los procedimientos de aplicacion de dichas composiciones. |
DE19537750A1 (de) * | 1995-10-10 | 1997-04-17 | Basf Ag | Oxiaminooximether, Verfahren und Zwischenprodukte zu ihrer Herstellung und sie enthaltende Mittel zur Bekämpfung von Schadpilzen und tierischen Schädlingen |
DE19539324A1 (de) * | 1995-10-23 | 1997-04-24 | Basf Ag | Phenylessigsäurederivate, Verfahren und Zwischenprodukte zu ihrer Herstellung und sie enthaltende Mittel |
DE19540361A1 (de) | 1995-10-30 | 1997-05-07 | Basf Ag | Phenylessigsäurederivate, Verfahren und Zwischenprodukte zu ihrer Herstellung und ihre Verwendung zur Bekämpfung von Schadpilzen und tierischen Schädlingen |
DE59604706D1 (de) * | 1995-11-02 | 2000-04-20 | Basf Ag | Pyridylessigsäurederivate, verfahren und zwischenprodukte zu ihrer herstellung und ihre verwendung |
DE19540989A1 (de) * | 1995-11-03 | 1997-05-07 | Basf Ag | Pyridylessigsäurederivate, Verfahren und Zwischenprodukte zu ihrer Herstellung und sie enthaltende Mittel |
AU723372B2 (en) | 1995-12-07 | 2000-08-24 | Bayer Aktiengesellschaft | Pesticides |
EP0876333B1 (en) * | 1995-12-07 | 2002-03-27 | Bayer Aktiengesellschaft | Process for the preparation of pesticides |
DE59605241D1 (de) | 1996-01-03 | 2000-06-21 | Novartis Ag | Verfahren zur Herstellung o-Chlor-Methyl-Phenylglyoxylsäure-Derivaten |
JP4170393B2 (ja) * | 1996-04-26 | 2008-10-22 | ビーエーエスエフ ソシエタス・ヨーロピア | 殺菌剤混合物 |
KR20000065017A (ko) * | 1996-04-26 | 2000-11-06 | 스타르크, 카르크 | 살진균제혼합물 |
WO1997040672A1 (de) * | 1996-04-26 | 1997-11-06 | Basf Aktiengesellschaft | Fungizide mischungen |
HUP9903721A3 (en) * | 1996-04-26 | 2001-08-28 | Basf Ag | Fungicide mixtures |
JP2000509062A (ja) * | 1996-04-26 | 2000-07-18 | ビーエーエスエフ アクチェンゲゼルシャフト | 殺菌剤混合物 |
EP0900012B1 (de) * | 1996-04-26 | 2002-03-27 | Basf Aktiengesellschaft | Fungizide mischungen |
ATE204132T1 (de) * | 1996-04-26 | 2001-09-15 | Basf Ag | Fungizide mischungen |
DK0900021T3 (da) * | 1996-04-26 | 2002-07-15 | Basf Ag | Fungicid blanding |
EP0900010B1 (de) * | 1996-04-26 | 2002-04-03 | Basf Aktiengesellschaft | Fungizide mischung |
NZ332078A (en) * | 1996-04-26 | 2000-05-26 | Basf Ag | Fungicides comprising synergistic mixtures of an acaricide with either a carbamate or an oxime ether or both |
WO1997040677A1 (de) * | 1996-04-26 | 1997-11-06 | Basf Aktiengesellschaft | Fungizide mischungen |
TW438575B (en) * | 1996-08-28 | 2001-06-07 | Basf Ag | Compositions and methods for controlling harmful fungi |
US6228810B1 (en) | 1996-09-18 | 2001-05-08 | Basf Ag | Pyridine derivatives, process for preparing the same and their use for controlling animal pests and harmful fungi |
AU6811698A (en) * | 1996-10-23 | 1998-05-15 | Novartis Ag | Pesticides |
DE19708940A1 (de) * | 1997-03-05 | 1998-09-10 | Basf Ag | Hydroximsäurehalogenide, Verfahren zur ihrer Herstellung und ihre Verwendung |
CO5050364A1 (es) * | 1997-05-28 | 2001-06-27 | Basf Ag | Metodo para controlar hongos nocivos |
WO1998054970A1 (de) | 1997-06-04 | 1998-12-10 | Basf Aktiengesellschaft | Fungizide mischungen |
DE19724200A1 (de) | 1997-06-09 | 1998-12-10 | Basf Ag | Bisiminosubstituierte Phenylverbindungen |
EP0934935A1 (de) | 1998-02-05 | 1999-08-11 | Basf Aktiengesellschaft | Heterocyclylsubstituierte Phenylverbindungen, Verfahren und Zwischenprodukte zu ihrer Herstellung und ihre Verwendung zur Bekämpfung von Schadpilzen und tierischen Schädlingen |
AU761132B2 (en) * | 1998-05-14 | 2003-05-29 | Basf Aktiengesellschaft | Bisoximether derivatives, methods and intermediate products for the production thereof, and their use for combating fungicidal pests and animal pests |
US6313344B1 (en) | 1998-05-27 | 2001-11-06 | Bayer Aktiengesellschaft | Organic compounds |
US6537989B1 (en) | 1998-10-15 | 2003-03-25 | Basf Aktiengesellschaft | Azadioxacycloalkene derivatives, methods for the production thereof and their use as fungicides and pest control agents |
GB9827163D0 (en) | 1998-12-10 | 1999-02-03 | Novartis Ag | Organic compounds |
EP1137627A1 (en) * | 1998-12-10 | 2001-10-04 | Bayer Aktiengesellschaft | Process for the preparation of strobilurin intermediates |
US6313339B1 (en) | 2000-02-17 | 2001-11-06 | Ronald Ross, Jr. | Aryl and heteroarylcylopropyl oxime ethers and their use as fungicides and insecticides |
DE10209145A1 (de) * | 2002-03-01 | 2003-09-04 | Bayer Cropscience Ag | Halogenbenzole |
PT1496745E (pt) * | 2002-04-10 | 2011-02-24 | Basf Se | Método para aumentar a resistência de plantas à fitotoxicidade de agroquímicos |
CN1711024A (zh) | 2002-11-12 | 2005-12-21 | 巴斯福股份公司 | 提高耐受草甘膦的豆类产率的方法 |
NZ567770A (en) * | 2005-10-28 | 2011-12-22 | Basf Se | Method of inducing resistance to harmful fungi |
CA2643701C (en) * | 2006-03-10 | 2016-02-02 | Basf Se | Method for improving the tolerance of plants to chilling temperatures and/or frost using a strobilurin compound |
BRPI0708283A2 (pt) * | 2006-03-14 | 2011-05-24 | Basf Se | método para induzir toleráncia contra bacterioses de plantas, e, uso das combinações |
PT2001294T (pt) | 2006-03-24 | 2017-01-13 | Basf Se | Método para combater fungos fitopatogénicos |
US20100234366A1 (en) * | 2006-03-29 | 2010-09-16 | Bsf Se | Use of Strobilurins for the Treatment of Disorders of Iron Metabolism |
JP2010524483A (ja) | 2007-04-23 | 2010-07-22 | ビーエーエスエフ ソシエタス・ヨーロピア | 化学物質とトランスジェニック改変とを組み合わせることによる植物生産性の増強 |
MX2009012880A (es) * | 2007-06-29 | 2009-12-10 | Basf Se | Estrobilurinas para aumentar la resistencia de plantas al estres abiotico. |
US20100272853A1 (en) * | 2007-12-21 | 2010-10-28 | Basf Se | Method of Increasing the Milk and/or Meat Quantity of Silage-Fed Animals |
TWI489941B (zh) * | 2008-09-19 | 2015-07-01 | Sumitomo Chemical Co | 種子處理劑及保護植物的方法 |
EP2458994A1 (en) | 2009-07-28 | 2012-06-06 | Basf Se | A method for increasing the level of free amino acids in storage tissues of perennial plants |
CN102510720A (zh) | 2009-09-25 | 2012-06-20 | 巴斯夫欧洲公司 | 降低植物中雌蕊花败育的方法 |
MX2017015558A (es) * | 2015-06-02 | 2018-02-23 | Syngenta Participations Ag | Composiciones para el control de vectores mosquitos, metodos y productos que utilizan las mismas. |
WO2020264016A1 (en) | 2019-06-25 | 2020-12-30 | Inari Agriculture, Inc. | Improved homology dependent repair genome editing |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1990007493A1 (de) * | 1988-12-29 | 1990-07-12 | F. Hoffmann-La Roche Ag | Aldimino- oder ketimino-oxy-ortho-tolylacrylsäure-methylester, ihre herstellung und diese enthaltende fungizide |
Family Cites Families (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CH632130A5 (en) * | 1977-03-02 | 1982-09-30 | Ciba Geigy Ag | Compositions on the basis of oxime ethers, oxime esters or oxime carbamates which are suitable in agriculture for crop protection |
DE3100728A1 (de) * | 1981-01-13 | 1982-08-26 | Bayer Ag, 5090 Leverkusen | Hydroximsaeureester, verfahren zu ihrer herstellung sowie ihre verwendung als fungizide |
ES2118769T3 (es) * | 1988-11-21 | 1998-10-01 | Zeneca Ltd | Fungicidas. |
DE3933891A1 (de) | 1989-10-11 | 1991-04-18 | Basf Ag | Phenylessigsaeure-derivate und diese enthaltende fungizide |
PH11991042549B1 (zh) * | 1990-06-05 | 2000-12-04 | ||
EP0463488B2 (de) * | 1990-06-27 | 2004-04-21 | BASF Aktiengesellschaft | O-Benzyl-Oximether und diese Verbindungen enthaltende Pflanzenschutzmittel |
GB9018408D0 (en) * | 1990-08-22 | 1990-10-03 | Ici Plc | Fungicides |
ES2088572T5 (es) * | 1991-01-30 | 2001-01-01 | Zeneca Ltd | Fungicidas. |
DE4103695A1 (de) * | 1991-02-07 | 1992-08-13 | Basf Ag | Oximether und diese enthaltende fungizide |
NZ242290A (en) * | 1991-04-15 | 1994-12-22 | Zeneca Ltd | Pyridyl and pyrimidinyl substituted oxime-o-benzyl ether derivatives; preparatory processes, fungicidal compositions and an intermediate |
US5286790A (en) * | 1992-03-10 | 1994-02-15 | The Dow Chemical Company | Acrylate polymers modified with poly(phenylene ether) |
AU690190B2 (en) * | 1994-01-05 | 1998-04-23 | Bayer Aktiengesellschaft | Pesticides |
PL179077B1 (en) * | 1994-02-04 | 2000-07-31 | Basf Ag | Derivatives of phenyloacetic acid, method of and intermediate products for obtaining them and agents containing such derivatives |
CH689228A5 (de) | 1994-10-07 | 1998-12-31 | Novartis Ag | Oximether, sowie diese enthaltende Pflanzenschutzmittel. |
-
1995
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-
1999
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-
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Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1990007493A1 (de) * | 1988-12-29 | 1990-07-12 | F. Hoffmann-La Roche Ag | Aldimino- oder ketimino-oxy-ortho-tolylacrylsäure-methylester, ihre herstellung und diese enthaltende fungizide |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104039144A (zh) * | 2011-11-30 | 2014-09-10 | 组合化学工业株式会社 | 乙二肟衍生物及有害生物防除剂 |
CN104039144B (zh) * | 2011-11-30 | 2015-09-16 | 组合化学工业株式会社 | 乙二肟衍生物及有害生物防除剂 |
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