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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591252Generated: October 31, 2026

4-(Trifluoromethyl)aniline → 2-(1,1-difluoropropyl)-5-methyl-N-[4-(trifluoromethyl)phenyl][1,2,4]triazolo[1,5-a]pyrimidin-7-amine

https://huagongshe.com/reaction/591252

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Trifluoromethyl)anilineHCID 9964—
Reactant7-Chloro-2-(1,1-difluoropropyl)-5-methyl[1,2,4]triazolo[1,5-a]pyrimidineHCID 53391980—
SolventEthanolHCID 702—
Product2-(1,1-difluoropropyl)-5-methyl-N-[4-(trifluoromethyl)phenyl][1,2,4]triazolo[1,5-a]pyrimidin-7-amineHCID 51347542—

Reaction Conditions

Temperature50 °C

Reaction Steps

A suspension of Intermediate 7 (0.1 g, 0.405 mmol) and 4-(trifluoromethyl)aniline (ALDRICH, 0.051 mL, 0.405 mmol) in ethanol (5 mL) was heated at 50° C. for 1 h. The reaction mixture was concentrated under vacuum, redissolved in DCM (20 mL) and washed with aq. Na2CO3 (2×15 mL). The organic layer was dried over anhydrous Na2SO4, filtered and concentrated under vacuum to afford a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238653B2
Source datasetuspto-grants-2016_01
ORD IDord-1d6cf148cb0142baa370c9079d677459
Source noteuspto-grants-2016_01