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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 901865Generated: October 30, 2026

Triethylamine → 5-Bromo-3,4-dihydro-3-methylquinazolin-2(1H)-one

https://huagongshe.com/reaction/901865

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTriphosgeneHCID 94429—
Reactant3-Bromo-2-methylaminomethyl-phenylamineHCID 18444472—
SolventDichloromethaneHCID 6344—
Product5-Bromo-3,4-dihydro-3-methylquinazolin-2(1H)-oneHCID 18444524—

Reaction Steps

To a solution of 3-bromo-2-methylaminomethyl-phenylamine (1.153 g, 5.36 mmol) in CH2Cl2 (50 ml) was added NEt3 (1.5 ml, 10.76 mmol), triphosgen (555 mg, 1.87 mmol) at 0° C. The reaction was allowed to warm up to room temperature and stirred overnight. After the solvent was removed by using a rotary evaporator, the residue was partitioned between water and ethyl acetate. The organic layer was washed by H2O and brine. After drying over MgSO4, the organic fraction was concentrated in vacuo and resulting brown residue was purified by flash chromatography to give 5-bromo-3-methyl-3,4-dihydro-1H-quinazolin-2-one as white solid. (650 mg, 50%) MS: (M+H)+ 241.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07365063B2
Source datasetuspto-grants-2008_04
ORD IDord-dd6443f37d3740c39cdbaf36a4c95a6c
Source noteuspto-grants-2008_04