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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1276597Generated: October 31, 2026

Triethylamine → 2-{4-[(2-Phenylimidazol-5-yl)methyl]piperazinyl}quinazoline

https://huagongshe.com/reaction/1276597

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Piperazin-1-yl-quinazolineHCID 6423266—
Reactant(2-Phenyl-1H-imidazol-5-yl)methanolHCID 10080865—
SolventThionyl ChlorideHCID 24386—
Product2-{4-[(2-Phenylimidazol-5-yl)methyl]piperazinyl}quinazolineHCID 992930386.4%

Reaction Steps

A sample of 2-phenyl-4-hydroxymethylimidazole (348 mg, 2 mmol) is heated for 5 min in thionyl chloride (5 mL) and subsequently concentrated. Chloroform (10 mL) is added and the solution reconcentrated. The resulting dark oil is then taken up in chloroform (10 mL) and treated with 1-quinazolin-2-ylpiperazine (428 mg, 2 mmol) and triethyl amine (2 mL). After 10 minutes, the reaction is washed with 2N NaOH solution, dried (Na2SO4) and concentrated to provide the title compound (Compound 4) as an oil (640 mg), the hydrochloride salt is prepared in a conventional manner, m.p. 101-105° C. (Compound 4a). 1H NMR (CDCl3) 9.0 (s, 1H), 7.9 (d, J=7 Hz, 2H), 7.65 (m, 2H), 7.55 (d, J=6 Hz, 1H), 7.2-7.4 (m, 4H), 7.0 (s, 1H, imidazole CH), 3.95 (m, 4H), 3.6 (s, 2H), 2.6 (t, J=5 Hz, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06166205
Source datasetuspto-grants-2000_12
ORD IDord-eddf2b4297e94ff8952007cd734576bb
Source noteuspto-grants-2000_12