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333761-24-3

ETHYL 5-(4-FLUOROPHENYL)-7-(TRIFLUOROMETHYL)PYRAZOLO[1,5-A]PYRIMIDINE-3-CARBOXYLATE synthesis

7synthesis methods
-

Yield:333761-24-3 76.63%

Reaction Conditions:

with glacial acetic acid at 115; for 7 h;

Steps:

3.1; 3.2; 3.3 synthesis of ethyl 5-(4-fluorophenyl)-7-trifluoromethylpyrazolo[1,5-a]pyrimidine-3-carboxylate.

Amino-1H-pyrazole-4-carboxylate obtained in the step 1) (15.58, 0.1 mmol) and the 1-p-fluorophenyl-4,4,4-tris Fluorobutanedione (23.4 g, 0.1 mol) was placed in a vessel;The mixture E was dissolved in 50 mL of glacial acetic acid to give a mixture E which was heated to 115 ° C under heating. The mixture was heated to reflux for 7 hours, cooled and allowed to stand, precipitating a yellow-green needlepoint Solid; the solid is filtered, washed, dried,Ethyl 5- (4-fluorophenyl) -7-trifluoromethylpyrazolo [l, 5- a] pyrimidine-3-carboxylate;The mass of the obtained product ethyl 5- (4-fluorophenyl) -7-trifluoromethylpyrazolo [1,5-a] pyrimidine-3-carboxylate was 27.05 g. Yield: 76.63%.

References:

CN105884783,2016,A Location in patent:Paragraph 0062; 0063; 0064; 0065; 0066