Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1590874Generated: October 27, 2026

Dichloromethane → N-(2-aminoethyl)-5-phenyl-4-thiazolecarboxamide hydrochloride

https://huagongshe.com/reaction/1590874

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTrifluoroacetic acidHCID 6422—
Reactantt-Butyl [2-(5-phenyl-4-thiazolecarboxamido)ethyl]carbamateHCID 53676915—
ProductN-(2-aminoethyl)-5-phenyl-4-thiazolecarboxamide hydrochlorideHCID 1976878594%

Reaction Steps

4.3 g (12.37 mmol) of t-butyl [2-(5phenyl-4-thiazolecarboxamido)ethyl]carbamate were dissolved in 10 ml of methylene chloride, treated with 5.0 ml of trifluoro- acetic acid and stirred at 20° for 16 hours and at 60° for 1 hour. Subsequently, the mixture was concentrated under reduced pressure. The residue was dissolved in 10 ml of ethanol, treated with 3 ml of 17.5% (w/v) ethanolic hydro- chloric acid and evaporated. The residue was recrystallized from methanol, whereby 3.3 g (94%) of N-(2-aminoethyl)-5-phenyl-4-thiazolecarboxamide hydrochloride were obtained as white crystals, melting pint 243°-245°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05204482
Source datasetuspto-grants-1993_04
ORD IDord-071ff91ef33b45ffb2aecc4e04eb68ff
Source noteuspto-grants-1993_04