首页> 外国专利> NEW 2-FLUORO-3-DE((2,6-DIDEOXY-3-C-METHYL-3-O-METHYL-ALPHA-L-RIBOHEXOPYRANOSYL)OXY)-6-O-METHYL-3-OXOERYTHROMYCIN DERIVATIVE, ITS PRODUCTION AND ITS USE FOR SYNTHESIZING ACTIVE INGREDIENT OF MEDICINE

NEW 2-FLUORO-3-DE((2,6-DIDEOXY-3-C-METHYL-3-O-METHYL-ALPHA-L-RIBOHEXOPYRANOSYL)OXY)-6-O-METHYL-3-OXOERYTHROMYCIN DERIVATIVE, ITS PRODUCTION AND ITS USE FOR SYNTHESIZING ACTIVE INGREDIENT OF MEDICINE

机译:新型2-氟-3-DE((2,6-二甲氧基-3-C-甲基-3-O-甲基-α-L-核糖基吡喃核糖基)氧基)-6-O-甲基-3-氧代凝血酶的衍生物及其生产及其在合成药物有效成分中的用途

摘要

PROBLEM TO BE SOLVED: To obtain the subject new derivative useful as a synthetic raw material for an active ingredient of a medicine, etc., comprising a specific 2-fluoro-3- oxoerythromycin derivative prepared by treating a 3-oxoerythromycin derivative with an electrophilic fluorinating agent. ;SOLUTION: This new 2-fluoro-3-[(2,6-dideoxy-3-C-methyl-3-O-methyl--L- ribohexopyranosyl)oxy]-6-O-methyl-3-oxoerythromycin derivative is shown by formula I (A is OH group and B forms a carbon-carbon double bond with a carbon atom at the 10-position or A and B are bonded to form a carbonate or a carbamate; OZ is a free esterified or etherified hydroxyl group). The compound is obtained by treating a compound of formula II with an electrophilic fluorinating agent such as N-fluoro-bis(phenylsulfonyl)imide or the like.;COPYRIGHT: (C)1999,JPO
机译:解决的问题:为了获得用作药物等活性成分的合成原料的本主题新衍生物,其包括通过用亲电子试剂处理3-氧代红霉素衍生物而制备的特定的2-氟-3-氧代红霉素衍生物。氟化剂。 ;解决方案:这种新的2-氟-3-[(2,6-dideoxy-3-C-methyl-3-O-methyl--L-ribohexopyranosyl)oxy] -6-O-methyl-3-oxoerythromycin衍生物是由式I表示(A是OH基,B形成在10位碳原子的碳-碳双键,或A和B键合形成碳酸酯或氨基甲酸酯; OZ是游离的酯化或醚化的羟基)。该化合物通过用亲电氟化剂如N-氟-双(苯磺酰基)酰亚胺等处理式II的化合物而获得。版权所有:(C)1999,JPO

著录项

  • 公开/公告号JPH11310591A

    专利类型

  • 公开/公告日1999-11-09

    原文格式PDF

  • 申请/专利权人 HOECHST MARION ROUSSEL;

    申请/专利号JP19990088580

  • 发明设计人 BONNET ALAIN;GAMBIER FRANCOISE;

    申请日1999-03-30

  • 分类号C07H17/08;

  • 国家 JP

  • 入库时间 2022-08-22 02:35:04

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