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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2283203Generated: October 31, 2026

Ethyl Bromide → HCID 178510891, compound

https://huagongshe.com/reaction/2283203

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl BromideHCID 6332—
Reactant2-Amino-4-chlorobenzoic acidHCID 66646—
Reactant2-CyanoethanethioamideHCID 1416277—
ReactantSodium ethoxideHCID 2723922—
ProductHCID 178510891HCID 17851089118.5%

Reaction Steps

2-cyanoethanethioamide (300 mg, 3.00 mmol) and bromoethane (299 μL, 4.00 mmol) were added to an ethanolic solution of sodium ethoxide (4.00 mmol, 3 mL). The resulting mixture was stirred for 6 hours, 2-amino-4-chlorobenzoic acid (500 mg, 2.91 mmol) was added, and the reaction was refluxed overnight with stirring. A solid precipitate formed upon cooling of the reaction mixture, which was recovered by vacuum filtration and washed sequentially with ethanol, water, ethanol, and diethyl ether. The solid was then dried to yield 2-(7-chloro-4-oxo-1,4-dihydroquinazolin-2-yl)acetonitrile (118 mg, 18%). 1H NMR (400 MHz, DMSO-d6) δ ppm 4.19 (s, 2H), 7.57 (dd, J1=8.5 Hz, J2=2.1 Hz, 1H), 7.74 (d, J=2.0 Hz, 1H), 8.09 (d, J=8.4 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145376B2
Source datasetuspto-grants-2015_09
ORD IDord-e7dc31e733c5445da22f22db72893ed5
Source noteuspto-grants-2015_09