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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 521663Generated: October 28, 2026

Dimethylformamide → 2-(2-Ethylsulfanylphenyl)-7-trifluoromethylquinazoline

https://huagongshe.com/reaction/521663

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantTert-Butyl nitriteHCID 10906—
Reactant4-Amino-2-(2-ethylsulfanylphenyl)-7-trifluoromethylquinazolineHCID 118205828—
SolventWaterHCID 962—
Product2-(2-Ethylsulfanylphenyl)-7-trifluoromethylquinazolineHCID 11803558415.3%

Reaction Conditions

Temperature100 °C

Reaction Steps

324 mg of t-butyl nitrite was added to a mixture of 506 mg of 4-amino-2-(2-ethylsulfanylphenyl)-7-trifluoromethylquinazoline and 10 ml of DMF at 100° C., and the mixture was stirred at 100° C. for 45 minutes. Water was added to the cooled reaction mixture, and the mixture was extracted with t-butyl methyl ether. The organic layer was washed with water and dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The resulting residue was applied to a silica gel column chromatography to obtain 74 mg of 2-(2-ethylsulfanylphenyl)-7-trifluoromethylquinazoline (Compound of Present Invention 11).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09328121B1
Source datasetuspto-grants-2016_05
ORD IDord-773220a852194f409f42db985e93e2e9
Source noteuspto-grants-2016_05