Process for the preparation of .beta.-(benzothiazolylthio)- and
.beta.-(benzimidazolylthio-carboxylic acids
    12.
    发明授权
    Process for the preparation of .beta.-(benzothiazolylthio)- and .beta.-(benzimidazolylthio-carboxylic acids 失效
    制备β-(苯并噻唑硫基) - 和β-(苯并咪唑基硫代羧酸)的方法

    公开(公告)号:US4612378A

    公开(公告)日:1986-09-16

    申请号:US610145

    申请日:1984-05-14

    摘要: The reaction of 2-mercapto-benzothiazole or -benzimidazole with .alpha.,.beta.-unsaturated carboxylic acids in a strongly acid reaction medium gives compounds of the formula I ##STR1## in which X is sulfur or NH, each radical R independently of one another is H, alkyl, halogenoalkyl, alkoxy, alkylthio, alkylsulfonyl, phenyl, alkylphenyl, phenylalkyl, cycloalkyl, halogen, NO.sub.2, CN, COOH, COOalkyl, OH or an amino or carbamyl group and R.sup.1, R.sup.2 and R.sup.3 independently of one another are H, alkyl, halogenoalkyl, hydroxyalkyl, alkoxyalkyl, carboxyalkyl, carboxyl or unsubstituted or substituted aryl or aralkyl, or R.sup.1 and R.sup.2 together are straight-chain or branched alkylene, which can be substituted by 1 or 2 carboxyl groups.

    摘要翻译: 在强酸反应介质中2-巯基苯并噻唑或苯并咪唑与α,β-不饱和羧酸的反应得到式I化合物,其中X为硫或NH,每个基团R彼此独立地为 烷基,卤代烷基,烷氧基,烷硫基,烷基磺酰基,苯基,烷基苯基,苯基烷基,环烷基,卤素,NO2,CN,COOH,COO烷基,OH或氨基或氨基甲酰基,R1,R2和R3彼此独立地为H 烷基,卤代烷基,羟基烷基,烷氧基烷基,羧基烷基,羧基或未取代或取代的芳基或芳烷基,或者R 1和R 2一起是可被1或2个羧基取代的直链或支链亚烷基。