UA68435C2 - Substituted benzoyl ketones and their use as herbicides - Google Patents

Substituted benzoyl ketones and their use as herbicides Download PDF

Info

Publication number: UA68435C2
Authority: UA; Ukraine
Prior art keywords: optionally substituted; carbon atoms; chlorine; methoxy; fluorine
Prior art date: 1999-05-08

Application number

UA2001128417A

Other languages

English (en)

Ukrainian (uk)

Original Assignee

Bayer Ag

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1999-05-08

Filing date

2000-04-26

Publication date

2004-08-16

2000-04-26 Application filed by Bayer Ag filed Critical Bayer Ag

2004-08-16 Publication of UA68435C2 publication Critical patent/UA68435C2/uk

Links

RXVBJUZEFSAYPW-UHFFFAOYSA-N 1,3-diphenylpropane-1,2,3-trione Chemical class C=1C=CC=CC=1C(=O)C(=O)C(=O)C1=CC=CC=C1 RXVBJUZEFSAYPW-UHFFFAOYSA-N 0.000 title claims abstract description 11
239000004009 herbicide Substances 0.000 title claims abstract description 7
-1 cyano, carbamoyl Chemical group 0.000 claims abstract description 346
229910052736 halogen Inorganic materials 0.000 claims abstract description 49
150000002367 halogens Chemical group 0.000 claims abstract description 49
239000001257 hydrogen Substances 0.000 claims abstract description 43
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 43
125000003545 alkoxy group Chemical group 0.000 claims abstract description 28
125000004390 alkyl sulfonyl group Chemical group 0.000 claims abstract description 23
125000004414 alkyl thio group Chemical group 0.000 claims abstract description 20
125000004644 alkyl sulfinyl group Chemical group 0.000 claims abstract description 18
125000000623 heterocyclic group Chemical group 0.000 claims abstract description 15
125000004663 dialkyl amino group Chemical group 0.000 claims abstract description 14
125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 13
125000000547 substituted alkyl group Chemical group 0.000 claims abstract description 12
125000003282 alkyl amino group Chemical group 0.000 claims abstract description 11
125000004453 alkoxycarbonyl group Chemical group 0.000 claims abstract description 9
125000004472 dialkylaminosulfonyl group Chemical group 0.000 claims abstract description 9
125000002947 alkylene group Chemical group 0.000 claims abstract description 5
125000005842 heteroatom Chemical group 0.000 claims abstract description 4
229920006395 saturated elastomer Polymers 0.000 claims abstract description 4
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 3
125000002619 bicyclic group Chemical group 0.000 claims abstract description 3
125000002950 monocyclic group Chemical group 0.000 claims abstract description 3
125000004430 oxygen atom Chemical group O* 0.000 claims abstract description 3
125000000464 thioxo group Chemical group S=* 0.000 claims abstract description 3
125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract 22
125000004043 oxo group Chemical group O=* 0.000 claims abstract 2
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 73
125000004432 carbon atom Chemical group C* 0.000 claims description 71
239000000460 chlorine Substances 0.000 claims description 56
229910052801 chlorine Inorganic materials 0.000 claims description 56
125000001153 fluoro group Chemical group F* 0.000 claims description 48
229910052731 fluorine Inorganic materials 0.000 claims description 46
239000011737 fluorine Substances 0.000 claims description 46
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 40
125000000217 alkyl group Chemical group 0.000 claims description 38
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 36
125000003506 n-propoxy group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])O* 0.000 claims description 36
150000001875 compounds Chemical class 0.000 claims description 34
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 32
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 30
125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 claims description 27
125000006125 ethylsulfonyl group Chemical group 0.000 claims description 25
125000003253 isopropoxy group Chemical group [H]C([H])([H])C([H])(O*)C([H])([H])[H] 0.000 claims description 22
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 22
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 19
229910052794 bromium Inorganic materials 0.000 claims description 19
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 17
229910052799 carbon Inorganic materials 0.000 claims description 15
125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 15
125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 14
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims description 11
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 11
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 10
125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims description 9
125000006216 methylsulfinyl group Chemical group [H]C([H])([H])S(*)=O 0.000 claims description 9
125000003342 alkenyl group Chemical group 0.000 claims description 8
125000000304 alkynyl group Chemical group 0.000 claims description 8
125000004093 cyano group Chemical group *C#N 0.000 claims description 8
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 8
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 8
125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 claims description 7
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 7
125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 6
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 6
125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 6
125000004186 cyclopropylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C1([H])[H] 0.000 claims description 6
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 5
CPPKAGUPTKIMNP-UHFFFAOYSA-N cyanogen fluoride Chemical compound FC#N CPPKAGUPTKIMNP-UHFFFAOYSA-N 0.000 claims description 5
125000005920 sec-butoxy group Chemical group 0.000 claims description 5
125000003258 trimethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])[*:1] 0.000 claims description 5
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 4
125000003302 alkenyloxy group Chemical group 0.000 claims description 4
HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 claims description 4
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 4
125000005605 benzo group Chemical group 0.000 claims description 4
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 4
125000000440 benzylamino group Chemical group [H]N(*)C([H])([H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims description 4
125000001316 cycloalkyl alkyl group Chemical group 0.000 claims description 4
125000006310 cycloalkyl amino group Chemical group 0.000 claims description 4
125000006001 difluoroethyl group Chemical group 0.000 claims description 4
125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 claims description 4
125000002534 ethynyl group Chemical group [H]C#C* 0.000 claims description 4
230000002363 herbicidal effect Effects 0.000 claims description 4
239000011630 iodine Substances 0.000 claims description 4
229910052740 iodine Inorganic materials 0.000 claims description 4
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 4
229910052760 oxygen Inorganic materials 0.000 claims description 4
239000001301 oxygen Substances 0.000 claims description 4
RGSFGYAAUTVSQA-UHFFFAOYSA-N pentamethylene Natural products C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 claims description 4
125000004817 pentamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 claims description 4
125000004368 propenyl group Chemical group C(=CC)* 0.000 claims description 4
125000002568 propynyl group Chemical group [*]C#CC([H])([H])[H] 0.000 claims description 4
150000003839 salts Chemical class 0.000 claims description 4
239000011734 sodium Substances 0.000 claims description 4
229910052708 sodium Inorganic materials 0.000 claims description 4
229910052717 sulfur Inorganic materials 0.000 claims description 4
125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 claims description 4
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 4
125000001246 bromo group Chemical group Br* 0.000 claims description 3
125000002510 isobutoxy group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])O* 0.000 claims description 3
125000006606 n-butoxy group Chemical group 0.000 claims description 3
125000004768 (C1-C4) alkylsulfinyl group Chemical group 0.000 claims description 2
125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 claims description 2
125000005236 alkanoylamino group Chemical group 0.000 claims description 2
125000006323 alkenyl amino group Chemical group 0.000 claims description 2
125000005108 alkenylthio group Chemical group 0.000 claims description 2
125000004448 alkyl carbonyl group Chemical group 0.000 claims description 2
125000004369 butenyl group Chemical group C(=CCC)* 0.000 claims description 2
125000000480 butynyl group Chemical group [*]C#CC([H])([H])C([H])([H])[H] 0.000 claims description 2
125000001309 chloro group Chemical group Cl* 0.000 claims description 2
125000004775 chlorodifluoromethyl group Chemical group FC(F)(Cl)* 0.000 claims description 2
125000002603 chloroethyl group Chemical group [H]C([*])([H])C([H])([H])Cl 0.000 claims description 2
125000000000 cycloalkoxy group Chemical group 0.000 claims description 2
125000005112 cycloalkylalkoxy group Chemical group 0.000 claims description 2
125000005366 cycloalkylthio group Chemical group 0.000 claims description 2
125000004850 cyclobutylmethyl group Chemical group C1(CCC1)C* 0.000 claims description 2
125000004210 cyclohexylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims description 2
125000004851 cyclopentylmethyl group Chemical group C1(CCCC1)C* 0.000 claims description 2
125000006003 dichloroethyl group Chemical group 0.000 claims description 2
125000004772 dichloromethyl group Chemical group [H]C(Cl)(Cl)* 0.000 claims description 2
125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 claims description 2
125000005448 ethoxyethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])C([H])([H])* 0.000 claims description 2
125000005745 ethoxymethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])* 0.000 claims description 2
125000004705 ethylthio group Chemical group C(C)S* 0.000 claims description 2
125000003784 fluoroethyl group Chemical group [H]C([H])(F)C([H])([H])* 0.000 claims description 2
QWPPOHNGKGFGJK-UHFFFAOYSA-N hypochlorous acid Chemical compound ClO QWPPOHNGKGFGJK-UHFFFAOYSA-N 0.000 claims description 2
125000005928 isopropyloxycarbonyl group Chemical group [H]C([H])([H])C([H])(OC(*)=O)C([H])([H])[H] 0.000 claims description 2
125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 claims description 2
125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 claims description 2
125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims description 2
125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 claims description 2
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 2
125000001424 substituent group Chemical group 0.000 claims description 2
239000011593 sulfur Substances 0.000 claims description 2
125000004434 sulfur atom Chemical group 0.000 claims description 2
125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 0.000 claims description 2
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical class [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims 4
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 2
125000004429 atom Chemical group 0.000 claims 2
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical class [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical class C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims 1
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IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
REEQLXCGVXDJSQ-UHFFFAOYSA-N trichlopyr Chemical compound OC(=O)COC1=NC(Cl)=C(Cl)C=C1Cl REEQLXCGVXDJSQ-UHFFFAOYSA-N 0.000 description 1
ZSDSQXJSNMTJDA-UHFFFAOYSA-N trifluralin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O ZSDSQXJSNMTJDA-UHFFFAOYSA-N 0.000 description 1
AKTQJCBOGPBERP-UHFFFAOYSA-N triflusulfuron Chemical compound FC(F)(F)COC1=NC(N(C)C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2C)C(O)=O)=N1 AKTQJCBOGPBERP-UHFFFAOYSA-N 0.000 description 1
235000001019 trigonella foenum-graecum Nutrition 0.000 description 1
YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 description 1
KVEQCVKVIFQSGC-UHFFFAOYSA-N tritosulfuron Chemical compound FC(F)(F)C1=NC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(F)(F)F)=N1 KVEQCVKVIFQSGC-UHFFFAOYSA-N 0.000 description 1
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239000011701 zinc Substances 0.000 description 1
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Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/44—Iso-indoles; Hydrogenated iso-indoles
- C07D209/48—Iso-indoles; Hydrogenated iso-indoles with oxygen atoms in positions 1 and 3, e.g. phthalimide
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/647—Triazoles; Hydrogenated triazoles
- A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- 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
- C07D213/02—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 having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—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 having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—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 having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/62—Oxygen or sulfur atoms
- C07D213/63—One oxygen atom
- C07D213/64—One oxygen atom attached in position 2 or 6
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D231/18—One oxygen or sulfur atom
- C07D231/20—One oxygen atom attached in position 3 or 5
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D233/70—One oxygen atom
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
- C07D237/26—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings condensed with carbocyclic rings or ring systems
- C07D237/30—Phthalazines
- C07D237/32—Phthalazines with oxygen atoms directly attached to carbon atoms of the nitrogen-containing ring
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/06—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D239/08—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms directly attached in position 2
- C07D239/10—Oxygen or sulfur atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
- C07D249/10—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D249/12—Oxygen or sulfur atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
- C07D249/10—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D249/14—Nitrogen atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D253/00—Heterocyclic compounds containing six-membered rings having three nitrogen atoms as the only ring hetero atoms, not provided for by group C07D251/00
- C07D253/02—Heterocyclic compounds containing six-membered rings having three nitrogen atoms as the only ring hetero atoms, not provided for by group C07D251/00 not condensed with other rings
- C07D253/04—1,2,3-Triazines
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/52—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings condensed with carbocyclic rings or ring systems
- C07D263/54—Benzoxazoles; Hydrogenated benzoxazoles
- C07D263/58—Benzoxazoles; Hydrogenated benzoxazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D275/00—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings
- C07D275/04—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings condensed with carbocyclic rings or ring systems
- C07D275/06—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings condensed with carbocyclic rings or ring systems with hetero atoms directly attached to the ring sulfur atom
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D285/00—Heterocyclic compounds containing rings having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by groups C07D275/00 - C07D283/00
- C07D285/01—Five-membered rings
- C07D285/02—Thiadiazoles; Hydrogenated thiadiazoles
- C07D285/04—Thiadiazoles; Hydrogenated thiadiazoles not condensed with other rings
- C07D285/12—1,3,4-Thiadiazoles; Hydrogenated 1,3,4-thiadiazoles
- C07D285/125—1,3,4-Thiadiazoles; Hydrogenated 1,3,4-thiadiazoles with oxygen, sulfur or nitrogen atoms, directly attached to ring carbon atoms, the nitrogen atoms not forming part of a nitro radical
- C07D285/13—Oxygen atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems

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Organic Chemistry (AREA)
Chemical & Material Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Environmental Sciences (AREA)
Agronomy & Crop Science (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Plant Pathology (AREA)
Pest Control & Pesticides (AREA)
Health & Medical Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Plural Heterocyclic Compounds (AREA)
Nitrogen Condensed Heterocyclic Rings (AREA)
Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Thiazole And Isothizaole Compounds (AREA)
Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
Pyridine Compounds (AREA)
Indole Compounds (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

UA2001128417A 1999-05-08 2000-04-26 Substituted benzoyl ketones and their use as herbicides UA68435C2 (en)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
DE19921424A DE19921424A1 (de)	1999-05-08	1999-05-08	Substituierte Benzoylketone
PCT/EP2000/003712 WO2000068204A1 (de)	1999-05-08	2000-04-26	Substituierte benzoylketone, verfahren zu ihrer herstellung und ihre verwendung als herbizide

Publications (1)

Publication Number	Publication Date
UA68435C2 true UA68435C2 (en)	2004-08-16

Family

ID=7907528

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
UA2001128417A UA68435C2 (en)	1999-05-08	2000-04-26	Substituted benzoyl ketones and their use as herbicides

Country Status (18)

Country	Link
US (1)	US6762152B1 (es)
EP (1)	EP1181280B1 (es)
JP (1)	JP2002544198A (es)
KR (1)	KR20020008394A (es)
CN (1)	CN1162405C (es)
AR (1)	AR023886A1 (es)
AT (1)	ATE283842T1 (es)
AU (1)	AU764182B2 (es)
BR (1)	BR0010388A (es)
CA (1)	CA2373076A1 (es)
DE (2)	DE19921424A1 (es)
ES (1)	ES2235868T3 (es)
HK (1)	HK1048115A1 (es)
MX (1)	MXPA01011357A (es)
PL (1)	PL351747A1 (es)
RU (1)	RU2245330C2 (es)
UA (1)	UA68435C2 (es)
WO (1)	WO2000068204A1 (es)

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US7842727B2 (en)	2001-03-27	2010-11-30	Errant Gene Therapeutics, Llc	Histone deacetylase inhibitors
DE10125432A1 (de) *	2001-05-25	2002-11-28	Bayer Ag	Substituierte Benzoylketone
CA2486402C (en)	2002-05-22	2013-04-30	Errant Gene Therapeutics, Llc	Histone deacetylase inhibitors based on alpha-chalcogenmethylcarbonyl compounds
EP1511477A4 (en)	2002-05-22	2008-04-09	Errant Gene Therapeutics Llc	HISTONE DEACETYLASE INHIBITORS BASED ON ALPHA-KETO-EPOXYDE COMPOUNDS
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DE102006024024A1 (de) *	2006-05-23	2007-11-29	Bayer Healthcare Aktiengesellschaft	Substituierte Arylimidazolone und -triazolone sowie ihre Verwendung
DE102008060967A1 (de) *	2008-12-06	2010-06-10	Bayer Schering Pharma Aktiengesellschaft	Substituierte Phenylsulfonyltriazolone und ihre Verwendung
DE102010001064A1 (de) *	2009-03-18	2010-09-23	Bayer Schering Pharma Aktiengesellschaft	Substituierte 2-Acetamido-5-Aryl-1,2,4-triazolone und deren Verwendung
HUE035761T2 (en)	2010-02-27	2018-05-28	Bayer Ip Gmbh	Bisaryl-linked aryltriazolones and their use
DE102010040187A1 (de)	2010-09-02	2012-03-08	Bayer Schering Pharma Aktiengesellschaft	Substituierte N-Phenethyl-triazolonacetamide und ihre Verwendung
DE102010040924A1 (de)	2010-09-16	2012-03-22	Bayer Schering Pharma Aktiengesellschaft	Substituierte Phenylacet- und Phenylpropanamide und ihre Verwendung
EA032137B1 (ru)	2014-11-03	2019-04-30	Байер Фарма Акциенгезельшафт	Производные гидроксиалкил-замещенного фенилтриазола и их применение
US9988367B2 (en)	2016-05-03	2018-06-05	Bayer Pharma Aktiengesellschaft	Amide-substituted pyridinyltriazole derivatives and uses thereof
CN107652217B (zh) *	2017-10-24	2019-09-03	青岛清原化合物有限公司	取代的苯甲酰基二酮腈类化合物或其互变异构体、盐、制备方法、除草组合物及应用

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1999
- 1999-05-08 DE DE19921424A patent/DE19921424A1/de not_active Withdrawn
2000
- 2000-04-26 MX MXPA01011357A patent/MXPA01011357A/es active IP Right Grant
- 2000-04-26 AU AU45563/00A patent/AU764182B2/en not_active Ceased
- 2000-04-26 WO PCT/EP2000/003712 patent/WO2000068204A1/de not_active Application Discontinuation
- 2000-04-26 DE DE50008845T patent/DE50008845D1/de not_active Expired - Fee Related
- 2000-04-26 PL PL00351747A patent/PL351747A1/xx not_active Application Discontinuation
- 2000-04-26 AT AT00927048T patent/ATE283842T1/de not_active IP Right Cessation
- 2000-04-26 CN CNB008100675A patent/CN1162405C/zh not_active Expired - Fee Related
- 2000-04-26 JP JP2000617184A patent/JP2002544198A/ja active Pending
- 2000-04-26 US US10/009,981 patent/US6762152B1/en not_active Expired - Fee Related
- 2000-04-26 BR BR0010388-8A patent/BR0010388A/pt not_active IP Right Cessation
- 2000-04-26 ES ES00927048T patent/ES2235868T3/es not_active Expired - Lifetime
- 2000-04-26 CA CA002373076A patent/CA2373076A1/en not_active Abandoned
- 2000-04-26 EP EP00927048A patent/EP1181280B1/de not_active Expired - Lifetime
- 2000-04-26 UA UA2001128417A patent/UA68435C2/uk unknown
- 2000-04-26 KR KR1020017013595A patent/KR20020008394A/ko not_active Application Discontinuation
- 2000-04-26 RU RU2001133347/04A patent/RU2245330C2/ru not_active IP Right Cessation
- 2000-05-08 AR ARP000102214A patent/AR023886A1/es unknown
2003
- 2003-01-10 HK HK03100258.4A patent/HK1048115A1/zh unknown

Also Published As

Publication number	Publication date
CN1360580A (zh)	2002-07-24
HK1048115A1 (zh)	2003-03-21
CA2373076A1 (en)	2000-11-16
DE19921424A1 (de)	2000-11-09
BR0010388A (pt)	2002-03-19
RU2245330C2 (ru)	2005-01-27
PL351747A1 (en)	2003-06-16
DE50008845D1 (de)	2005-01-05
EP1181280B1 (de)	2004-12-01
CN1162405C (zh)	2004-08-18
US6762152B1 (en)	2004-07-13
MXPA01011357A (es)	2002-05-06
AU4556300A (en)	2000-11-21
KR20020008394A (ko)	2002-01-30
ES2235868T3 (es)	2005-07-16
JP2002544198A (ja)	2002-12-24
AU764182B2 (en)	2003-08-14
WO2000068204A1 (de)	2000-11-16
AR023886A1 (es)	2002-09-04
EP1181280A1 (de)	2002-02-27
ATE283842T1 (de)	2004-12-15

Publication	Publication Date	Title
UA68435C2 (en)	2004-08-16	Substituted benzoyl ketones and their use as herbicides
EP1100789B1 (de)	2005-02-09	Substituierte benzoylcyclohexandione
KR100693373B1 (ko)	2007-03-12	제초제로서의 치환된 벤조일피라졸
EP1178987B1 (de)	2003-08-13	Substituierte benzoylisoxazole und ihre verwendung als herbizide
JP2000514805A (ja)	2000-11-07	置換芳香族カルボニル化合物及びそれらの誘導体
US6573219B1 (en)	2003-06-03	Substituted heterocyclyl-2H-chromenes
JP2003506449A (ja)	2003-02-18	置換チエニル（アミノ）スルホニルウレア
CA2333068A1 (en)	1999-12-02	Sulfonyl amino (thio)carbonyl triazoline (thi)ons having alkenyl substituents
RU2248352C2 (ru)	2005-03-20	Замещенные бензоилциклогександионы, гербицидное средство на их основе, исходное соединение
US6608004B2 (en)	2003-08-19	Substituted 2-aryl-1,2,4-triazine-3,5-di(thi)ones
CA2070717A1 (en)	1992-12-08	Substituted imidazolinylpyrimidines
JP2001506245A (ja)	2001-05-15	ヘテロシクリルウラシル
US6350720B2 (en)	2002-02-26	Substituted phenyltriazolin(THI)ones and their use as herbicides
KR100730004B1 (ko)	2007-06-20	치환된 벤조일사이클로헥세논
DE19917160A1 (de)	2000-10-19	Disubstituierte Pyridine und Pyrimidine
JP2002515492A (ja)	2002-05-28	置換１，３−ジアザ−２−（チ）オキソ−シクロアルカン
JP2002543099A (ja)	2002-12-17	Ｎ−置換ヘテロシクリルアルキルアミン類の除草剤としての使用及び新規なｎ−置換チエニルアルキルアミン類
UA77414C2 (en)	2006-12-15	Substituted arylketones, intermediary compound for the preparation thereof, herbicide agent
MXPA01000519A (es)	2001-11-21	Benzoilciclohexandionas substituidas