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1-{[4-(trifluoromethyl)phenyl]methyl}-1H-pyrazol-3-amine synthesis

1synthesis methods
1820-80-0 Synthesis
3-Aminopyrazole

1820-80-0
465 suppliers
$5.00/5g

402-49-3 Synthesis
4-(TRIFLUOROMETHYL)BENZYL BROMIDE

402-49-3
268 suppliers
$5.00/1g

1-{[4-(trifluoromethyl)phenyl]methyl}-1H-pyrazol-3-amine

1240572-94-4
4 suppliers
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Yield:1240572-94-4 56%

Reaction Conditions:

with sodium carbonate in acetonitrile at 50; for 6 h;

Steps:

15.A

A suspension of 3-aminopyrazole (0.77 g, 9.27 mmol) and compound 10-8 (2.44 g, 10.21 mmol) in acetonitrile (40 mL) was treated with sodium carbonate (2.46 g, 23.18 mmol), and then the mixture was heated To 50°C,And kept at this temperature for 6h. Cool the mixture to 25°C,And filter out the insoluble matter. The supernatant was concentrated and purified by column chromatography (0% to 50% methanol/dichloromethane) to obtain pure product 8-9 (1.25g, 56%):

References:

CN113493442,2021,A Location in patent:Paragraph 0271-0274