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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250607Generated: October 29, 2026

Triethylamine → 4-Allylamino-2-(2,2,2-trifluoroethylamino)-6-nitroquinazoline

https://huagongshe.com/reaction/1250607

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthanamine, 2,2,2-trifluoro-HCID 9773—
Reactant4-Allylamino-2-chloro-6-nitroquinazolineHCID 18326487—
Product4-Allylamino-2-(2,2,2-trifluoroethylamino)-6-nitroquinazolineHCID 1832656230.8%

Reaction Steps

A mixture of 150 mg (0.57 mmol) of 4-allylamino-2-chloro-6-nitroquinazoline, 772 mg (5.70 mmol) of 2,2,2-trifluoroethylamine and 1.15 g (11.4 mmol) of triethylamine was stirred in a sealed tube at room temperature for 16 hours. After completion of the reaction, ice water was added to the reaction mixture, followed by extraction with chloroform (10 ml×3). After the organic layer was washed with brine and then dried over anhydrous sodium sulfate, the solvent was distilled off under reduced pressure. The residue was purified by a silica gel chromatography to give 57 mg (yield: 30.8%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06339089B2
Source datasetuspto-grants-2002_01
ORD IDord-755905076abf4007b5bf965e0139a8f0
Source noteuspto-grants-2002_01