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Isocyanato-benzoxazoles-benzothiazoles and benimidazoles - as anthelmintics and antimicrobials

机译:异氰酸酯-苯并恶唑-苯并噻唑和苯并咪唑-驱虫药和抗菌药

摘要

Cpds (I) (where SCN occupies positions 4,5,6 or 7, R1 is H, 1-17C alkyl or alkenyl opt. substd. by CN, halogen, OH, Oalkyl, acyl, Salkyl or dialkylamino contg. up to a total of 6C, a mono-, bi- or tricyclic cycloalkyl or cycloalkenyl contg. 3-10 intracyclic C atoms and opt. substd. by alkyl gps. the cyclic radical opt. being linked to Y or to the heterocyclic residue by CH2-, R2 is H, halogen or 1-4C-alkyl, -Oalkyl or -acyl, X is O, S or NR3, R3 is H, 1-5C-alkyl or -alkenyl, Ph, PhCH2, dimethyl- or diethyl-amino-(2-5C-alkyl), 2-5C-alkoxycarbonyl or acyl or polyhydroxy alkyl (ose or oside), Y is O, S, SO SO2 or N-R4, n is 0 or 1, R4 is H, 1-5C-alkyl or -alkenyl, or together with the N-atom and R1 is a 4-, 5- or 6-membered heterocyclic ring opt. contg. a further O, S or NR5 residue and R5 is H, Me or Et) are prepd. by various methods from the corresponding amino cpd. or by cyclising an isothiocyanato-2-acylamino phenol, which cpd. also forms part of the invention.
机译:Cpds(I)(其中SCN占据4,5,6或7位,R1为H,1-17C烷基或烯基,优选被CN,卤素,OH,O烷基,酰基,S烷基或二烷基氨基取代,最高达1)总共6C,一个单环,双环或三环的环烷基或环烯基,包含3-10个环内C原子,并且用烷基gps取代,该环上的自由基通过Y2-与Y或杂环残基相连, R 2为H,卤素或1-4C-烷基,-O烷基或-酰基,X为O,S或NR 3,R 3为H,1-5C-烷基或-烯基,Ph,PhCH 2,二甲基-或二乙基-氨基- (2-5C-烷基),2-5C-烷氧羰基或酰基或多羟基烷基(糖或羟基),Y为O,S,SO SO2或N-R4,n为0或1,R4为H,1-5C -烷基或-烯基,或与N原子和R1一起为4、5或6元杂环,另选一个O,S或NR5残基,R5为H,Me或Et准备通过各种方法从相应的氨基cpd中获得。或环化cpd的异硫氰酸根合-2-酰基氨基苯酚。也构成本发明的一部分。

著录项

  • 公开/公告号CH565164A5

    专利类型

  • 公开/公告日1975-08-15

    原文格式PDF

  • 申请/专利权人 CIBA-GEIGY AG;

    申请/专利号CH19740016464

  • 发明设计人

    申请日1971-12-07

  • 分类号C07D277/62;A01N9/18;

  • 国家 CH

  • 入库时间 2022-08-23 04:07:28

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