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Synthesis of Antidiabetic Medicine Repaglinide

ZHAO Shuang1, XU Zhibing1, E Chenguang1, LI Zhuo1, WANG Ensi1,2   

  1. 1. College of Life Science, Jilin University, Changchun 130021, China; 2. College of Pharmacy, Jilin University, Changchun 130021, China
  • Received:2007-06-28 Revised:1900-01-01 Online:2008-05-26 Published:2008-05-26
  • Contact: WANG Ensi

Abstract: Repaglinide (a new antidiabetic medicine), (S)(+)-2-ethoxy-4-[N-[1-(2-piperidinophenyl)-3-methyl-1-butyl]aminocarbo nylmethyl]benzoic acid, was synthesized by means of Ph3P catalyzed condensation and LDA/DMPU catalyzed carboxylation as pivotal steps from the starting materials 4-methylsalicylic acid and 2-chlorobenzonitrile. Repaglinide was synthesized in a total yield of 10.5%. The structures of the targetmolecule and the key intermediates were confirmed by IR, 1H NMR,13C NMR, elemental analysis, specific rotation and MS techniques.

Key words: repaglinide, chemical resolution technique, optical r otation, antidiabetic medicine

CLC Number: 

  • R977.15