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6-chloro-4-oxo-1,4-dihydroquinoline-2-carboxylic acid synthesis

2synthesis methods
-

Yield:24796-59-6 47%

Reaction Conditions:

Stage #1: methyl 6-chloro-4-oxo-1,4-dihydroquinoline-2-carboxylatewith lithium hydroxide monohydrate;sodium hydroxide in tetrahydrofuran; for 16 h;
Stage #2: with aqueous citric acid in tetrahydrofuran;lithium hydroxide monohydrate;

References:

Yoshikawa, Kenji;Kobayashi, Shozo;Nakamoto, Yumi;Haginoya, Noriyasu;Komoriya, Satoshi;Yoshino, Toshiharu;Nagata, Tsutomu;Mochizuki, Akiyoshi;Watanabe, Kengo;Suzuki, Makoto;Kanno, Hideyuki;Ohta, Toshiharu [Bioorganic and Medicinal Chemistry,2009,vol. 17,# 24,p. 8221 - 8233] Location in patent:experimental part