Matsumoto - Google Patents

Mikio Hori, Tadashi Kataoka, Hiroshi Shimizu, Eiji Imai, Yukiharu Matsumoto, and Masanori Kawachi Gifu College Of Pharmacy, 5-6-Japan

Matsumoto

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Document ID: 4420335131617360068
Author: Matsumoto Y

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Mikio Hori , Tadashi Kataoka, Hiroshi Shimizu, Eiji Imai, Yukiharu Matsumoto, and Masanori Kawachi Gifu College Of Pharmacy, 5-6 Page 1 HETEROCYCLES, Vd. 19, No. Mikio Hori , Tadashi Kataoka, Hiroshi Shimizu, Eiji Imai, Yukiharu Matsumoto, and Masanori Kawachi Gifu …

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 O=C1NC(=O)NC2=C1NC=N2 0 abstract description 10

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- 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
- C07D207/34—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 heteroatoms 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
- 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 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 C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
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- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
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- 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
- C07D207/18—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 one double bond between ring members or between a ring member and a non-ring member
- C07D207/22—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 one double bond between ring members or between a ring member and a non-ring member 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
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Publication	Publication Date	Title
KR100535450B1 (en)	2006-03-30	Preparation of pyrimidine derivatives
Zanatta et al.	2002	Synthesis of 4‐(trihalomethyl) dipyrimidin‐2‐ylamines from β‐alkoxy‐α, β‐unsaturated trihalomethyl ketones
Matsumoto	0	Mikio Hori, Tadashi Kataoka, Hiroshi Shimizu, Eiji Imai, Yukiharu Matsumoto, and Masanori Kawachi Gifu College Of Pharmacy, 5-6-Japan
Nikolaenkova et al.	2018	Synthesis and study of the azide-tetrazole tautomerism in 2-azido-4-(trifluoromethyl)-6-R-pyrimidines (R= H, 4-ClC 6 H 4)
Wendelin et al.	1984	Dihydropyrimidines and related structures. I. N2‐substituted 2‐pyrimidinamines and dihydro‐2‐pyrimidinamines by reaction of phenylbutenones and monosubstituted guanidines
Pilli et al.	1983	Reaction of N-(p-tolylsulfonyl) diphenylcyclopropenimine with pyridinium and isoquinolinium ylides
Wang et al.	2000	A new approach to the synthesis of heteroannulated 3, 1-oxazin-4-ones from β-enamino esters and phosgeneiminium salts
Dick et al.	1981	Heterocyclic compounds with bridgehead nitrogen atoms. Part 9. Synthesis in the pyrrolo [2, 1, 5-de] quinolizine ([2.3. 3] cyclazine) series starting from indolizines
Köckritz et al.	1994	Synthesis of pyrazolo [1, 5‐a] pyridines and pyrazolo [1, 5‐c] pyrimidines by reaction of heterocyclic amidrazones with 1, 3‐dicarbonyl compounds
Anderson et al.	1977	Pyridopyrimidines. 6. Nucleophilic substitutions in the pyrido [2, 3-d] pyrimidine series
EP1222184B1 (en)	2006-11-02	Preparation and use of gamma-butyrolactones as cross-linking agents
MacMillan et al.	1975	Further investigations of the interaction of trimethylsilyl azide with substituted maleic anhydrides. Synthesis of 4‐and 5‐aryl substituted 1, 3‐(3H) oxazine‐2, 6‐diones
Kojima et al.	1980	One‐step preparation of 3‐alkoxypyrazine‐2‐carbonitriles from pyrazine‐2, 3‐dicarbonitriles and related reactions
EP0704429B1 (en)	1998-06-10	2-(Aryliminomethyl)-3-(disubstituted amino)acrylonitriles, a process for their preparation and their use
US3808225A (en)	1974-04-30	Process for the preparation of 4(5)-cyanoimidazole-5(4)-carboxyamide by reacting diaminomaleonitrile with formic acid
YAMAMOTO et al.	1984	1, 3-Oxazines and Related Compounds. VIII. Reaction of 6-Methyl-2-phenyl-4H-1, 3-oxazin-4-one with Lactams and Their Derivatives
EP0584491B1 (en)	1995-05-03	Process for the production of 2,5-disubstituted pyridines
Mittelbach et al.	1980	Syntheses with nitriles. 60. Preparation of 4‐amino‐5‐cyano‐6‐phenylpyrimidines from 2‐amino‐1, 1‐dicyano‐2‐phenylethene
Ibrahim et al.	1985	Nitrile bei organischen Synthesen: Die Reaktion von Trichloracetonitril mit aktiven Methylen-Reagentien
Rahman et al.	2013	A One Pot Synthesis of 5, 7-diaryl-1, 5-dihydro (or 1, 2, 3, 5-tetrahydro)-pyrano [2, 3-D] pyrimidin-2, 4-diones (or 2-thioxo-4-ones)
SENDA et al.	1978	Pyrimidine Derivatives and Related Compounds. XXX.: Synthesis and Some Reactions of 5, 6-Dicyano-1, 3-dimethyluracil
JPS6136270A (en)	1986-02-20	Manufacture of 2_alkyl_4,5_dihydroxymethylimidazole
Yamato et al.	1982	REACTION OF ETHYL 0-ALKYLAMINOCROTONATES IN THE PRESENCE OF ORGANIC ACID
Nikolaenkova et al.	1997	Synthesis of 4, 6-bis (1H-1, 2, 3-triazolyl) pyrimidines by the reaction of 4, 6-diazido-2-(4-methoxyphenyl)-pyrimidine with compounds containing a reactive methylene group
Reddy et al.	1995	Fluoro organics: synthesis of novel fluorinated 4-oxo-4H-pyrido [3′, 2′: 4, 5] furo [3, 2-d]-1, 3-oxazines and their reactions

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