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1-PYRIDIN-2-YL-1H-PYRAZOLE-4-CARBOXYLIC ACID synthesis

5synthesis methods
-

Yield:77556-50-4 96%

Reaction Conditions:

with water;lithium hydroxide in tetrahydrofuran;ethanol at 0 - 20; for 7 h;

Steps:

B.65.2

Step 2: 1-Pyridin-2-yl-1H-pyrazol-4-carboxylic acidPyridin-2-yl-1H-pyrazol-4-carboxylic acid ethyl ester (0.81 g, 3.73 mmol) was dissolved in a THF/ethanol (50 ml/10 ml) mixture, cooled to 0° C. and treated with lithium hydroxide (11.2 ml, 1N aqueous solution). The reaction mixture was allowed to warm-up to ambient temperature and subsequently stirred at that temperature for 7 h. The reaction mixture was extracted with dichloromethane (4×100 ml) and the combined organic phases were dried and evaporated to yield the product as white solid (0.68 g, 96%) which was used without any further purification.MS: M=188.2 (M-H)-

References:

US2011/183979,2011,A1 Location in patent:Page/Page column 40-41