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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Piperazin-1-yl-quinazoline | HCID 6423266 | — |
| Reactant | (2-Phenyl-1H-imidazol-5-yl)methanol | HCID 10080865 | — |
| Solvent | Thionyl Chloride | HCID 24386 | — |
| Product | 2-{4-[(2-Phenylimidazol-5-yl)methyl]piperazinyl}quinazoline | HCID 9929303 | 86.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06166205 |
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| Source dataset | uspto-grants-2000_12 |
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| ORD ID | ord-eddf2b4297e94ff8952007cd734576bb |
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| Source note | uspto-grants-2000_12 |
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