Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2412479Generated: November 1, 2026

3-(1H-imidazol-2-yl)propan-1-ol → 2-Fluoro-4-[3-(fur-2-yl)carbamoyloxypropyl]-1-triphenylmethylimidazole

https://huagongshe.com/reaction/2412479

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(1H-imidazol-2-yl)propan-1-olHCID 17925287—
Reactant4-(3-Acetylcarbamoyloxypropyl)-2-fluoro-1-triphenylmethylimidazoleHCID 20432407—
Product2-Fluoro-4-[3-(fur-2-yl)carbamoyloxypropyl]-1-triphenylmethylimidazoleHCID 20432394—

Reaction Steps

A suspension of 2-furoamide in 1,2-dichloroethane was treated with oxalyl chloride; 2-furoylisocyanate was isolated by distillation. This product was reacted with the hydroxypropylimidazole, as for the starting material of Example 12, to give 2-fluoro-4-[3-(fur-2-yl)carbamoyloxypropyl]-1-triphenylmethylimidazole, having the following n.m.r. spectrum in d6DMSO: 1.82 (m, 2H); 2.47 (t, 2H); 4.07 (t, 2H); 6.3 (s, 1H); 6.64 (m, 1H); 7.0-7.45 (m, 15H); 7.5 (m, 1H); 7.91 (m, 1H); 10.1 (br, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04492692
Source datasetuspto-grants-1985_01
ORD IDord-2e043327950e442eb5b50a35644ffebe
Source noteuspto-grants-1985_01