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1-(3-fluorophenyl)-1H-pyrazole-4-carboxylic acid synthesis

3synthesis methods
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Yield:138907-82-1 88%

Reaction Conditions:

Stage #1: ethyl 5-amino-1-(3-fluorophenyl)-1H-pyrazole-4-carboxylatewith Isovaleronitrile in tetrahydrofuran;Reflux;
Stage #2: with methanol;lithium hydroxide in tetrahydrofuran;

References:

WO2014/41007,2014,A1 Location in patent:Page/Page column 19-20