Abstract
Norfloxacin ethyl ester was prepared from 3-chloro-4-fluoroaniline in ionic liquid in a one-pot procedure by condensation with EMME [ethoxymethylenemalonic diethyl ester], cyclization, ethylation and condensation with anhydrous piperazine. After its hydrolysis, norfloxacin was obtained with an overall yield of 72.7%.
Keywords: Synthesis, norfloxacin ethyl ester, ionic liquid
Letters in Organic Chemistry
Title: One-Pot Synthesis of Norfloxacin Ethyl Ester from 3-Chloro-4- Fluoroaniline in Ionic Liquid
Volume: 5 Issue: 1
Author(s): Shengdong Zhu, Yuanxin Wu, Ziniu Yu, Xizhou Shen, Chengmiao Xu, Jun Yao, Hong Huang and Shiwei Jin
Affiliation:
Keywords: Synthesis, norfloxacin ethyl ester, ionic liquid
Abstract: Norfloxacin ethyl ester was prepared from 3-chloro-4-fluoroaniline in ionic liquid in a one-pot procedure by condensation with EMME [ethoxymethylenemalonic diethyl ester], cyclization, ethylation and condensation with anhydrous piperazine. After its hydrolysis, norfloxacin was obtained with an overall yield of 72.7%.
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Cite this article as:
Zhu Shengdong, Wu Yuanxin, Yu Ziniu, Shen Xizhou, Xu Chengmiao, Yao Jun, Huang Hong and Jin Shiwei, One-Pot Synthesis of Norfloxacin Ethyl Ester from 3-Chloro-4- Fluoroaniline in Ionic Liquid, Letters in Organic Chemistry 2008; 5 (1) . https://dx.doi.org/10.2174/157017808783330126
DOI https://dx.doi.org/10.2174/157017808783330126 |
Print ISSN 1570-1786 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6255 |
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