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The production manner and miticidal medicine null of okisa (thiums) zorijin

机译:冲佐里金的生产方式和杀螨药

摘要

NEW MATERIAL:The compound of formula I [R1 is lower alkyl;R2 is phenyl which may have substituent group (halogen, lower alkyl, lower haloalkyl, lower alkoxy, lower haloalkoxy or methylenedioxy); group of formula V is a 5-7- membered heterocyclic group wherein the constituent atom of the ring may be substituted with a lower alkyl composed of C2-6, O0-1, N1-2; X and Y are O or S]. EXAMPLE:5-(4-Chlorophenyl)-4-methyl-3-piperidinocarbamoyl-2-thiazolidone. USE:Miticide. PREPARATION:The compound of formula I can be produced by a) reacting the compound of formula II with a phosgenation agent in an organic solvent in the presence of a base at a temperature between -20 deg.C and the boiling point of the solvent, preferably between 0 deg.C and room temperature for 30 min- several hr and b) reacting the resultant compound of formula III without separat ing from the reaction mixture with the compound of formula IV under the above conditions.
机译:新材料:式I化合物[R1为低级烷基; R2为可具有取代基的基团(卤素,低级烷基,低级卤代烷基,低级烷氧基,低级卤代烷氧基或亚甲基二氧基);式V的基团是5-7元杂环基,其中环的构成原子可被由C2-6,O0-1,N1-2组成的低级烷基取代; X和Y为O或S]。实施例:5-(4-氯苯基)-4-甲基-3-哌啶基氨基甲酰基-2-噻唑烷酮。用途:杀螨剂。制备:式I化合物可通过以下方法制备:a)式II化合物与光气化剂在有机溶剂中,在碱的存在下,在-20℃至溶剂的沸点之间的温度下反应,优选在0℃和室温之间保持30分钟-数小时,并且b)在上述条件下使所得的式III化合物反应而没有从反应混合物与式IV化合物分离。

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