首页> 外国专利> BENZOTHIADIAZINE DERIVATIVES THEIR PREPARATION AND VETERINARY AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM

BENZOTHIADIAZINE DERIVATIVES THEIR PREPARATION AND VETERINARY AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM

机译:苯并噻二嗪衍生物及其衍生物,兽药和兽药成分

摘要

1340428 Benzothiadiazine derivatives IMPERIAL CHEMICAL INDUSTRIES Ltd 13 March 1972 [13 April 1971] 9224/71 Heading C2C Novel benzothiadiazine derivatives of the Formula I wherein RSP1/SP is C 1-3 alkyl, RSP2/SP is H or RSP3/SPCO, wherein RSP3/SP is C 1-3 alkyl or phenyl optionally substituted by CH 3 or halogen, RSP4/SP, which is in 6- or 7-position of the benzothiadiazine nucleus, is benzoyl or phenylsulphonyl optionally substituted by CH 3 or halogen and n is 0 or 1, are prepared by one of the following methods: (a) for compounds in which n is 0, oxidizing aminophenylthioureas of the formula RSP4/SP is in the p-position relative to one or other of the substituents; (b) for compounds in which n is 0 and RSP2/SP is H, reducing nitrophenylthioureas of the Formula II above in which NHRSP2/SP is replaced by NO 2 with alkali metal dithionites in alkaline solutions; (c) for compounds in which RSP2/SP is RSP3/SPCO, acylating the corresponding compounds of Formula I above in which RSP2/SP is H; (d) reacting compounds of Formula I above in which COORSP1/SP is replaced by H with compounds of the formula wherein X is halogen; (e) for compounds in which n is 1, oxidizing the corresponding compounds of Formula I above in which n is 0 with peracids. Methyl 2 - amino - 4 - benzoylphenylthiocarbamoylcarbamate is obtained by reducing methyl 2 - nitro - 4 - benzoylphenylthiocarbamoylcarbamate, resulting from the reaction between 4-benzoyl-2-nitroaniline and methyl isothiocyanatoformate. Methyl 2 - amino - 5 - benzoylphenylthiocarbamoylcarbamate is prepared by reacting methyl isothiocyanatoformate with 2-amino- 4-benzoylaniline, obtained by reducing 4- benzoyl-2-nitro-aniline. Methyl 2 - nitro - 4 - phenylsulphonylphenylthiocarbamoylcarbamate is made by reacting methyl isothiocyanatoformate with 2-nitro-4- phenylsulphonylaniline, obtained hydrolysing ethyl 2 - nitro - 4 - phenylsulphonyphenylcarbamate, resulting from the nitration of ethyl 4 - phenylsulphonylphenylcarbamate, which is prepared by reacting 4-phenylsulphonylaniline with ethyl chloroformate. Methyl 2 - acetylamino -4 - benzoylphenylthiocarbamoylcarbamate is made by acetylating methyl 2-amino-4-benzoylphenylthiocarbamoylcarbamate. Methyl 2 - nitro - 5 - benzoylphenylthiocarbamoylcarbamate is obtained by reacting methyl isothiocyanatoformate with 5-benzoyl- 2-nitroaniline resulting the treatment of 5-nitro- 2-nitrochlorobenzene with a solution of ammonia in methenol under pressure. Anthelmintic compositions contain the above novel benzothiadiazine derivatives together with suitable diluents or carriers. The compositions are in forms suitable for oral or parenteral administration.
机译:1340428苯并噻二嗪衍生物帝国化学工业有限公司1972年3月13日[1971年4月13日]标题C2C其中R 1 为C 1-3烷基,R 2 < / SP>为H或R 3 CO,其中R 3 为C 1-3烷基或苯基,可选地被CH 3或卤素取代,R 4 位于苯并噻二嗪核的6或7位,是可被CH 3或卤素取代的苯甲酰基或苯磺酰基,n为0或1,可通过以下方法之一制备:(a)用于化合物当n为0时,相对于一个或另一个取代基,式R 4 的氧化氨基苯基硫脲处于对位; (b)对于n为0且R 2 为H的化合物,用碱金属连二亚硫酸盐将NHR 2 替换为NO 2的上述式II的还原硝基苯基硫脲在碱性溶液中; (c)对于其中R 2 是R 3 CO的化合物,酰化上面相应的其中R 2 是H的式I化合物; (d)使其中COOR 1 被H取代的上述式I化合物与其中X为卤素的式I化合物反应; (e)对于其中n为1的化合物,用过酸氧化上面其中n为0的相应的式I化合物。甲基2-氨基-4-苯甲酰基苯基硫代氨基甲酰基氨基甲酸酯是通过还原4-硝基苯甲酰基-2-硝基苯胺与异硫氰酸甲酯基甲酸甲酯反应生成的2-硝基-4-苯甲酰基苯基硫代氨基甲酰基氨基甲酸甲酯而获得的。通过使异硫氰酸甲酯甲基甲酸甲酯与通过还原4-苯甲酰基-2-硝基苯胺获得的2-氨基-4-苯甲酰基苯胺反应来制备2-氨基-5-苯甲酰基苯基硫代氨基甲酰基氨基甲酸甲酯。甲基2-硝基-4-苯基磺酰基苯基硫代氨基甲酰基氨基甲酸酯是通过使异硫氰酸甲基甲酸甲酯与2-硝基-4-苯基磺酰基苯胺反应,水解乙基2-硝基-4-苯基磺酰基苯基氨基甲酸酯而得到的,是将4-苯基磺酰基苯基氨基甲酸酯乙基化而制得的。 -苯基磺酰基苯胺与氯甲酸乙酯。甲基2-乙酰氨基-4-苯甲酰基苯基硫代氨基甲酰基氨基甲酸酯是通过将2-氨基-4-苯甲酰基苯基硫代氨基甲酰基氨基甲酸酯甲基化而制备的。通过使异硫氰酸氨基甲酸甲酯与5-苯甲酰基-2-硝基苯胺反应,得到2-甲基-硝基-5-苯甲酰基苯基硫代氨基甲酰基氨基甲酸甲酯,在压力下用氨在甲醇中的溶液处理5-硝基-2-硝基氯苯。驱虫药组合物包含上述新型苯并噻二嗪衍生物以及合适的稀释剂或载体。该组合物为适合于口服或肠胃外给药的形式。

著录项

  • 公开/公告号DE000002215733A

    专利类型

  • 公开/公告日1972-10-26

    原文格式PDF

  • 申请/专利权人

    申请/专利号DE2215733A

  • 发明设计人

    申请日1972-03-30

  • 分类号C07D91/68;

  • 国家 DE

  • 入库时间 2022-08-23 08:23:40

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