首页> 外国专利> 2 - substituted 4 - alkylamino 6 square bracket (small alpha, little alphadimethyl) - (beta - acetyl) - aethylamino square bracket to 1,3,5 - triazine and their use, and processes for producing the same

2 - substituted 4 - alkylamino 6 square bracket (small alpha, little alphadimethyl) - (beta - acetyl) - aethylamino square bracket to 1,3,5 - triazine and their use, and processes for producing the same

机译:2-取代的4-烷基氨基6方括号(小α,小的α二甲基)-(β-乙酰基)-1,3,5-三嗪的乙氨基方括号及其用途及其制备方法

摘要

2-Substituted-4-alkylamino-6-( alpha , alpha -dimethyl- beta -acetyl-ethylamino-1,3,5-triazines of the general formula (I) wherein X represents chlorine or a methylthio group, R represents hydrogen or a C1-4 alkyl group, and R' stands for a C1-4 alkyl or alkenyl group, of excellent herbicidal activities are prepared as follows: cyanurchloride is reacted with diacetonamine in a molar ratio of 1:1 in an aqueous or organic solvent medium in the presence of an acid binding agent, the thus-obtained 2,4-dichloro-6-( alpha , alpha -dimethyl- beta -acetyl-ethylamino)-1,3,5-triazine is reacted with an amine of the general formula NHRR' in the presence of an acid binding agent, and if a 2-methylthio compound is to be prepared, the thus-obtained 2-chloro-4-alkylamino-6-( alpha , alpha -dimethyl- beta -acetyl-ethylamino)-1,3,5-triazine is reacted with thiourea and the obtained product is methylated, or the 2-chloro compound is reacted with methylthiol.
机译:通式(I)的2-取代的-4-烷基氨基-6-(α,α-二甲基-β-乙酰基-乙基氨基-1,3,5-三嗪,其中X代表氯或甲硫基,R代表氢或具有优异除草活性的C1-4烷基,R'表示C1-4烷基或链烯基,其制备方法如下:在水或有机溶剂介质中,氰尿酰氯与二丙酮胺以1:1的摩尔比反应在酸结合剂的存在下,将如此获得的2,4-二氯-6-(α,α-二甲基-β-乙酰基-乙基氨基)-1,3,5-三嗪与通常的胺反应。在酸结合剂存在下制备式NHRR′,如果要制备2-甲硫基化合物,则如此获得的2-氯-4-烷基氨基-6-(α,α-二甲基-β-乙酰基-乙基氨基-1,3,5-三嗪与硫脲反应,得到的产物被甲基化,或2-氯化合物与甲硫醇反应。

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