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2,3-二氢-2-苯基咪唑[2,1-b]苯并噻唑的合成研究

Synthesis of 2,3-dihydro-2-phenyl-imidazo [2,1-b]benzothiazole (benzotetramisole)
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摘要 以2-氯苯并噻唑为原料,在N,N-二异丙基乙基胺存在下与D或L-苯甘氨醇反应后,不经分离直接与甲磺酰氯在N,N-二异丙基乙基胺作用下关环,一锅法合成了(R)或(S)-2,3-二氢-2-苯基咪唑[2,1-b]苯并噻唑,利用IR、1HNMR、MS谱和旋光度对其结构进行了表征。通过优化研究2,3-二氢-2-苯基咪唑[2,1-b]苯并噻唑的合成工艺条件,可得到总收率为80%的(R)或(S)-2,3-二氢-2-苯基咪唑[2,1-b]苯并噻唑。 A one-pot synthesis of acyl transfer catalyst benzotetramisole was achieved by the reaction of 2-chlorobenzothiazole with D or L-phenylglycinol in the presence of N,N-diisopropyl ethylamine,followed by subsequent cyclization in the presence of methanesulfonyl chloride.The structures of the compounds were characterized by IR,^1HNMR,MS spectra and optical rotation analysis.The experimental results showed that the products were (R)-or (S)-2,3-dihydro-2-phenyl-imidazo[2,1-b]benzothiazole and their yields were 80% under the reaction conditions.
出处 《化学试剂》 CAS CSCD 北大核心 2010年第4期293-295,298,共4页 Chemical Reagents
基金 国家自然科学基金资助项目(20602007)
关键词 2-氯苯并噻唑 苯甘氨醇 2 3-二氢-2-苯基咪唑[2 1-b]苯并噻唑 一锅法合成 2-chlorobenzothiazole phenylglycinol 2 3-dihydro-2-phenyl-imidazo[2 1-b]benzothiazole one-pot synthesis
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参考文献6

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