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Condensn products of erythromycyl-amine with aldehydes - antibiotic erythromycin derivs active against gram negative and gram positive bacteria

机译:红霉素胺与醛的缩合产物-抗生素红霉素对革兰氏阴性菌和革兰氏阳性菌具有活性

摘要

Erythromycin derivs. of formulae (I) (Ia) and (Ib) and their acid addition salts are novel. R=hydroxy, phenoxy, phenyl 1-3C alkoxy, 1-4C alkoxy a gp. hydroxyalkoxy, alkoxyalkoxy, dialkylaminoalkoxy or alkoxycarbonylalkoxy having 1-4C atoms in the alkylene part and 1-3C atoms in the alkyl part, mercapto, phenylmercapto (opt. substd. by methyl, methoxy, ethoxy, isopropoxy ro propoxy), phenyl-1-3 alkylmercapto, 1-5C straight or branched, alkylmercapto, cyclohexylmercapto, a gp. hydroxyalkylmercapto, dialkylaminomercapto, alkoxycarbonylalkylmercapto or cyanoalkylmercapto in each case having 1-3C in the alkyl or alkylene parts, -NR2R3, R4-COO, -NH-CO-R5, N-phenylcarbamoyl, R6R7-N-CO-CH2-O-, (R8O)2=P(O)-, -NH-SO2-R9 or -SO2-R10; R2, R3=H, phenyl phenyl-1-3C alkyl, 1-4C alkyl or NR2R3 form a 5-6 membered monocyclic heterocyclic opt. contg. a O or S or another N; R4=(un)branched 1-5C alkyl, benzyl or phenyl; R5=(un)branched 1-5c alkyl opt. substd. by 1 or 2 halo atoms or by a cyano gp., phenyl-1-3C-alkyl opt. substd. in the phenyl ring by 1-2 halo atoms or by a methoxy gp. and in the alkylene part by a halo atom, phenoxy-1-3C alkyl, phenyl-2-4C alkenyl, phenyl(opt. substd. by methyl, hydroxy, methoxy, nitro or chloro gps.), pyridyl, furyl, fluorofuryl or thienyl; R6,R7=methyl, ethyl, propyl or isopropyl; R8=(un)branched 1-5c alkyl, R9=1-4C alkyl or phenyl opt. substd. by a 1-3c alkyl; and R10=1-3C alkyl or phenyl opt. substd. by a 1-3C alkyl gps. Cpds. are antibacterials having good activity against Gram. positive and Gram-negative organisms.
机译:红霉素衍生。式(I)(Ia)和(Ib)的化合物及其酸加成盐是新颖的。 R =羟基,苯氧基,苯基1-3C烷氧基,1-4C烷氧基a gp。在亚烷基部分具有1-4C原子,在烷基部分具有1-3C原子的羟基烷氧基,烷氧基烷氧基,二烷基氨基烷氧基或烷氧基羰基烷氧基,巯基,苯基巯基(优选被甲基,甲氧基,乙氧基,异丙氧基或丙氧基取代),苯基-1- 3烷基巯基,1-5C直链或支链,烷基巯基,环己基巯基,gp。分别在烷基或亚烷基部分具有1-3C的羟烷基巯基,二烷基氨基巯基,烷氧基羰基烷基巯基或氰基烷基巯基,-NR2R3,R4-COO,-NH-CO-R5,N-苯基氨基甲酰基,R6R7-N-CO-CH2-O-, (R8O)2 = P(O)-,-NH-SO2-R9或-SO2-R10; R 2,R 3 = H,苯基苯基-1-3C烷基,1-4C烷基或NR 2 R 3形成5-6元单环杂环opt。续O或S或另一个N; R4 =(un)支链的1-5C烷基,苄基或苯基; R5 =(un)支链的1-5c烷基。取代通过1或2个卤素原子或通过氰基,优选苯基-1-3C-烷基。取代在苯环中具有1-2个卤原子或甲氧基gp。在亚烷基部分中,由卤素原子,苯氧基-1-3C烷基,苯基-2-4C烯基,苯基(优选由甲基,羟基,甲氧基,硝基或氯基gps取代),吡啶基,呋喃基,氟呋喃基或噻吩基R6,R7 =甲基,乙基,丙基或异丙​​基; R8 =(非)支链的1-5c烷基,R9 = 1-4C烷基或苯基。取代1-3c烷基; R10 = 1-3C烷基或苯基。取代通过1-3C烷基gps。 Cpds。是对革兰氏有良好活性的抗菌剂。阳性和革兰氏阴性生物。

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