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机构地区:[1]School of Pharmacy, Shandong University, Jinan 250012
出 处:《Chinese Chemical Letters》2006年第6期714-716,共3页中国化学快报(英文版)
基 金:we are grateful to the National Natural Science Foundation of China(No.20372043)for flnancial support for this Work.
摘 要:Novel ethyl 7-chloro-6-fluoro-l-methyl-4-oxo-1, 4-dihydro-[1, 3]thiazeto[3, 2-a]quino- line-3-carboxylate 2 was prepared from 3-chloro-4-fluoroaniline in eight steps. It can be used as a new intermediate for the synthesis of tricyclic fluoroquinolones.Novel ethyl 7-chloro-6-fluoro-l-methyl-4-oxo-1, 4-dihydro-[1, 3]thiazeto[3, 2-a]quino- line-3-carboxylate 2 was prepared from 3-chloro-4-fluoroaniline in eight steps. It can be used as a new intermediate for the synthesis of tricyclic fluoroquinolones.
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