发明名称 PROCESS FOR THE PREPARATION OF TRIAZAPENTADIENE
摘要 <p>1448165 1 - Substituted - 5 - (substituted phenyl) - 3 - methyl - 1,3,5 - triazapenta - 1,4- dienes and their acaricidal compositions PFIZER Ltd 21 Aug 1975 [23 Aug 1974] 37232/74 Heading C2C The invention comprises compounds of general Formula I and their salts with weak dibasic organic acids wherein R<SP>1</SP> is a C 1-4 alkyl group; R<SP>2</SP> is a hydrogen or halogen atom or a C 1-4 alkyl group; R<SP>3</SP> is a C 4-10 cycloalkyl group optionally substituted by a halogen atom or a C 1-4 alkyl group, a C 1-4 alkyl group substituted by an aryl group; or a C 1-4 alkyl group substituted by a C 4-10 cycloalkyl group, said cycloalkyl group optionally being substituted by a C 1-4 alkyl group or a halogen atom and R<SP>4</SP> is a hydrogen atom, a C 1-4 alkyl group or a group of formula SR<SP>5</SP> in which R<SP>5</SP> is a hydrogen atom or a C 1-4 alkyl group. Compounds of Formula I in which R<SP>4</SP> is hydrogen may be prepared by reacting a formamidine of Formula II with an isonitrite of formula R<SP>3</SP> NC in the presence of a catalyst such as CuO or Cu 2 Cl 2 . Compounds in which R<SP>4</SP> is a hydrogenation or a C 1-4 alkyl group may be prepared (a) by reacting a compound of Formula II (above) with an imidate of Formula III in which R<SP>6</SP> is a C 1-4 alkyl group by heating; (b) by heating a compound of Formula IV in which R<SP>7</SP> is a C 1 alkyl group with an amidine of Formula V or (c) by reacting an amidine of Formula III (above) with an isonitrile of Formula VI in the presence of a catalyst, e.g. CuO or Cu 2 <SP>1</SP>Cl 2 . Compounds of Formula I in which R<SP>4</SP> is a group of formula SR<SP>5</SP> may be prepared by reacting a formamidine of Formula II (above) with an isothiocyanate of formula R<SP>3</SP>NCS to obtain a product in which R<SP>5</SP> is hydrogen followed, if desired by 5-alkylation. N - Cyclohexyl - N<SP>1</SP> - methylacetamidine is obtained by reaction of methyl N-methylacetimidate with cyclohexylamine. N-Cyclohexylformamide is prepared by reaction of formic acid with cyclohexylamine and is further reacted with triethyloxanium fluorborate to obtain ethyl N-cyclohexylformimidate. N - Methyl - N<SP>1</SP> - (2,4 - dimethylphenyl)- formamidine is prepared by reaction of 2,4- xylidine hydrochloride with N-methylformamide in the presence of benzenesulphonylchloride. Acaricidal and insecticidal compositions comprise a compound of Formula I together with a diluent or carrier.</p>
申请公布号 IN142002(B) 申请公布日期 1977.05.14
申请号 IN1532CA1975 申请日期 1975.08.05
申请人 PFIZER CORP 发明人 PENROSE ALEXANDER BALLINGALL;LEEMING MICHAEL RAYMOND GRAVES
分类号 A01N37/52;A01N;A01N35/10;A01N47/32;A01P7/02;A61K;C07C;C07C23/00;C07C67/00;C07C239/00;C07C251/00;C07C257/10;C07C325/00;C07C335/32;C07C335/34;C07C335/38;C07D;(IPC1-7):C07C119/00 主分类号 A01N37/52
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