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Antimicrobial screening and synthesis of some novel benzo[a]phenothiazines and ribofuranosides

机译:某些新型苯并[a]吩噻嗪和呋喃核糖苷的抗菌筛选与合成

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摘要

Synthesis of 6-(4-chloro-2-methoxy-5-methylanilino/2-methoxy-5-methylanilino)-9-chloro-5H-benzo[a]phenothiazin-5-thione,12H-benzo[a] phenothiazin-5-ols,5-acetoxy-12H-benzo[a] phenothiazines and 5-methoxy-12H-benzo[a]pheno-thiazines have been carried out from 6-(4-chloro-2-methoxy-5-methylanilino/2-methoxy-5-methylanilino)-9-chloro-5H-benzo[a] phenothiazin-5-ones;which have been synthesized by condensing zinc mercaptide of 2-amino-5-chloro-benzenethiol and 2-(4-chloro-2-methoxy-5-methylanilino/2-methoxy-5-methylanilino)-3-chloro-1,4-naphthoquinone.The ribofuranosides viz,N-(2',3',5'-tri-O-bcnzoyl-beta-D-ribofuranosyl)-6-(4-chloro-2-methoxy-5-methylanilino/2-methoxy-5-methylanilino)-9-chloro-5-acctoxy/5-mcthoxy-12H-benzo[a]phenothiazines have been synthesized by condensing synthesized hetcrocycles bases with (+)-beta-D-ribofuranose-1-acctate-2,3,5-tribenzoate.Structural assignments have been done on the basis of elemental analysis,IR,and ~1H NMR.All the synthesized compounds have been screened for their antimicrobial activity.
机译:合成6-(4-氯-2-甲氧基-5-甲基苯胺基/ 2-甲氧基-5-甲基苯胺基)-9-氯-5H-苯并[a]吩噻嗪-5-硫酮,12H-苯并[a]吩噻嗪-从6-(4-氯-2-甲氧基-5-甲基苯胺基/ 2)制得5-醇,5-乙酰氧基-12H-苯并[a]吩噻嗪和5-甲氧基-12H-苯并[a]吩噻嗪-甲氧基-5-甲基苯胺基)-9-氯-5H-苯并[a]吩噻嗪-5-酮;它是通过将2-氨基-5-氯-苯硫醇的巯基锌与2-(4-氯- 2-甲氧基-5-甲基苯胺基/ 2 /甲氧基-5-甲基苯胺基)-3-氯-1,4-萘醌。呋喃核糖苷,即N-(2',3',5'-tri-O-bcnzoyl-beta -D-呋喃核糖基)-6-(4-氯-2-甲氧基-5-甲基苯胺基/ 2-甲氧基-5-甲基苯胺基)-9-氯-5-乙酰氧基/ 5-甲氧基-12H-苯并[a]吩噻嗪通过将合成的杂环化合物碱基与(+)-β-D-呋喃核糖-1-酸-2,3,5-三苯甲酸酯缩合而合成。结构分配基于元素分析,IR和〜1H NMR进行。合成的化合物是sc由于其抗菌活性而变得柔软。

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