Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1902318Generated: November 2, 2026

Triethylamine → 2-[4-(2-[2-(2,2,2-Trifluoroethyl)guanidino]thiazol-4-yl)butylamino]benzimidazole

https://huagongshe.com/reaction/1902318

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-[2-(2,2,2-Trifluoroethyl)-guanidino]-4-[4-(3-[2-aminophenyl]thioureido)butyl]thiazoleHCID 21298698—
CatalystSilver NitrateHCID 24470—
SolventDimethylformamideHCID 6228—
Product2-[4-(2-[2-(2,2,2-Trifluoroethyl)guanidino]thiazol-4-yl)butylamino]benzimidazoleHCID 21298802—

Reaction Steps

A mixture of 2-[2-(2,2,2-trifluoroethyl)-guanidino]-4-[4-(3-[2-aminophenyl]thioureido)butyl]thiazole (0.45 g.), silver nitrate (0.34 g.) and triethylamine (0.28 ml.) in dimethylformamide (3 ml.) was stirred vigorously at ambient temperature overnight. Hydrogen sulphide gas was then bubbled through the reaction mixture until no more solid precipitated. The reaction mixture was filtered through a pad of diatomaceous earth and the filtrate evaporated to dryness in vacuo. The residue was purified by low pressure liquid chromatography using chloroform/methanol/ammonia, 9:1:0.1 v/v/v as eluant to give 2-[4-(2-[2-(2,2,2-trifluoroethyl)guanidino]thiazol-4-yl)butylamino]benzimidazole which was converted to the hydrogen maleate salt (0.25 g.), mp. 183°-186°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04362728
Source datasetuspto-grants-1982_12
ORD IDord-15a69dbcd22e425681a5952bf07e4499
Source noteuspto-grants-1982_12