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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 386646Generated: October 29, 2026

2,2,2-Trifluoroethanol → 4-(4-(2,6-dimethyl-4-(pyridin-4-yl)phenoxy)-1H-pyrazolo[3,4-d]pyrimidin-6-ylamino)benzonitrile

https://huagongshe.com/reaction/386646

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2,2-TrifluoroethanolHCID 6409—
ReactantTrifluoroacetic acidHCID 6422—
Reactant4-AminobenzonitrileHCID 13396—
ReactantHCID 178422825HCID 178422825—
Product4-(4-(2,6-dimethyl-4-(pyridin-4-yl)phenoxy)-1H-pyrazolo[3,4-d]pyrimidin-6-ylamino)benzonitrileHCID 44123989—

Reaction Conditions

Temperature90 °C

Reaction Steps

Trifluoroacetic acid (8 eq) is added to a suspension of 7-(2,6-dimethyl-4-(pyridin-4-yl)phenoxy)-5-chloro-1H-[1,2,3]triazolo[4,5-d]pyrimidine (1 eq) and 4-aminobenzonitrile (4 eq) in 2,2,2-trifluoroethanol (1 ml/0.1 mmol) in a sealed tube. The resulting mixture is heated at 90° C. for 3 days. The reaction is cooled to room temperature, concentrated to dryness and purified by silica gel chromatography.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372852B2
Source datasetuspto-grants-2013_02
ORD IDord-6f5a18608c6e494c95a1b72620d8c01c
Source noteuspto-grants-2013_02