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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1509958Generated: November 2, 2026

Trifluoroacetic acid → 4-(2-(4-Cyanophenylamino)thieno[2,3-d]pyrimidin-4-yloxy)-3,5-dimethylbenzonitrile

https://huagongshe.com/reaction/1509958

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant4-AminobenzonitrileHCID 13396—
Reactant4-(2-Chlorothieno[2,3-d]pyrimidin-4-yloxy)-3,5-dimethylbenzonitrileHCID 57848878—
SolventEthyl AcetateHCID 8857—
Product4-(2-(4-Cyanophenylamino)thieno[2,3-d]pyrimidin-4-yloxy)-3,5-dimethylbenzonitrileHCID 2479508114.5%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of 4-(2-chlorothieno[2,3-d]pyrimidin-4-yloxy)-3,5-dimethylbenzonitrile (188 mg, 0.59 mmol), TFA (0.37 mL, 4.75 mmol) in TFE (2.5 mL) was added 4-aminobenzonitrile (280 mg, 2.37 mmol) in a scaled tube. The reaction was stirred at 90° C. for 2 d. Reaction-mixture was diluted with ethyl acetate (5 mL) and washed with saturated NaHCO3 (3×10 mL). The combined organic layers were washed with brine, dried over Na2SO4, filtered and concentrated in vacuo. The crude product was purified by HPLC afforded the product as white solid (34 mg, 14%):

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08211898B2
Source datasetuspto-grants-2012_07
ORD IDord-89ea0d87ff574afa9382ecb228e88f46
Source noteuspto-grants-2012_07