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new terms for framstellning of 7 - aminotiazolyl - acetamido - cefalosporansyraderivat

机译:7-氨基噻唑基-乙酰氨基-头孢洛氨吡喃衍生物的新术语

摘要

Syn 7-[2-(2-protected-amino-4- thiazolyl)-2-substituted-imino- acetamido]-ceph-3-em-4-carboxylic acid derivatives, which have pharmacological activity or may be used in the preparation of pharmacologically-active compounds, are prepared by reacting a syn 2-(2- protected-amino-4-thiazolyl)-2- substituted-imino-acetic acid or salt thereof with a compound of the general formula: IMAGE (wherein Y represents a tosyl or mesyl ion and Z represents a halogen ion, Y and Z each represent a tosyl ion, or Y and Z each represent a mesyl ion) and optionally treating the product with a base, so as to obtain the corresponding syn 2-(2-protected- amino-4-thiazolyl)-2-substituted- iminoacetoxy-tris(dimethylamino)- phosphonium salts, which salt is thereafter treated, optionally in the presence of a base, with an optionally 3/4 substituted 7-amino- cephalosporanic acid, or S-oxo or S,S- dioxo derivative, or a salt or ester thereof, and then treated with an acid. The acylation of the phosphonium salt is preferably carried out in an organic solvent below 0 DEG C, or in an aqueous solvent at ambient temperature.
机译:具有药理活性或可用于制备的Syn 7- [2-(2-保护基氨基-4-噻唑基)-2-取代的亚氨基-乙酰胺基] ceph-3-em-4-羧酸衍生物药理活性化合物的制备是通过使2-(2-被保护的氨基-4-噻唑基)-2-取代的亚氨基乙酸或其盐与通式为的化合物反应而制备的(其中Y代表甲苯磺酰基或甲磺酰基离子,Z代表卤素离子,Y和Z各自代表甲苯磺酰基离子,或Y和Z各自代表甲苯磺酰基离子),并且任选地用碱处理产物,以获得相应的syn 2 -(2-保护的-氨基-4-噻唑基)-2-取代的-亚氨基乙酰氧基-三(二甲基氨基)-phospho盐,其后任选在碱存在下用任选的3/4取代的7-盐处理该盐。氨基-头孢烷酸,或S-氧代或S,S-二氧代衍生物,或其盐或酯,然后用酸处理。 salt盐的酰化优选在低于0℃的有机溶剂中或在室温下在水性溶剂中进行。

著录项

  • 公开/公告号SE7906605L

    专利类型

  • 公开/公告日1980-04-24

    原文格式PDF

  • 申请/专利权人 ROUSSEL UCLAF;

    申请/专利号SE19790006605

  • 发明设计人 JOLLY J;WARNANT J;

    申请日1979-08-06

  • 分类号C07D501/06;C07D501/20;C07D501/36;

  • 国家 SE

  • 入库时间 2022-08-22 18:18:58

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