首页> 外国专利> Method for the preparation of 4-amino-6-tert. butyl-3-methylthio-1,2,4-triazin-5(4H)-one

Method for the preparation of 4-amino-6-tert. butyl-3-methylthio-1,2,4-triazin-5(4H)-one

机译:制备4-氨基-6-叔丁基的方法。丁基-3-甲硫基1,2,4-三嗪-5(4H)-一

摘要

The herbicidally active compound 4-amino-6-tert-butyl-3-methylthio-1,2,4-triazin-5- (4H) -one (I) is obtained by firstly using pivaloyl cyanide, (CH3) 3C- CO-CN (II), with a carboxylic anhydride of the general formula R-CO-O-CO-R (III), in which R represents an optionally substituted aliphatic radical having up to 8 carbon atoms or an optionally substituted phenyl radical, in the presence a strong acid and optionally in the presence of a solvent at temperatures between -50 and 150 ° C and the reaction mixture thus obtained is then reacted directly with thiocarbohydrazide (NH2-NH-CS-NH-NH2) (IV) and the 4-amino formed -6-tert-butyl-3-mercapto-1,2,4-triazin-5- (4H) -one (V) is separated off and in a second step this intermediate (V) is methylated in the usual way.
机译:首先通过使用新戊酰氰化物(CH3)3C-CO获得除草活性化合物4-氨基-6-叔丁基-3-甲硫基1,2,4-三嗪-5-(4H)-(I) -CN(II),具有通式R-CO-O-CO-R(III)的羧酸酐,其中R代表具有至多8个碳原子的任选取代的脂族基团或任选取代的苯基基团,在强酸的存在下以及视情况在-50至150°C之间的溶剂存在下,然后将如此获得的反应混合物与硫代碳酰肼(NH2-NH-CS-NH-NH2)(IV)直接反应,分离形成4-氨基的-6-叔丁基-3-巯基-1,2,4-三嗪-5-(4H)-一个(V),然后在第二步中将该中间体(V)在通常的方式。

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