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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 32848Generated: October 30, 2026

Trifluoroacetic acid → 2-amino-N,N-dimethyl-1,3-thiazole-4-carboxamide

https://huagongshe.com/reaction/32848

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant(4-Dimethylcarbamoyl-thiazol-2-yl)-carbamic acid tert-butyl esterHCID 86603401—
SolventDichloromethaneHCID 6344—
Product2-amino-N,N-dimethyl-1,3-thiazole-4-carboxamideHCID 54594297—

Reaction Steps

To a solution of (4-dimethylcarbamoyl-thiazol-2-yl)-carbamic acid tert-butyl ester (0.26 g, 0.95 mmol) in dichloromethane (10 mL) was added trifluoroacetic acid (10 mL, 130 mmol). The reaction mixture was stirred at room temperature for 2 hours, then concentrated under reduced pressure. Saturated aqueous sodium bicarbonate solution (50 mL) was added to neutralize the residue. The mixture was extracted with ethyl acetate (2×100 mL). The organic layers were separated, combined and dried over sodium sulfate, concentrated under reduced pressure and dried in vacuo to give crude 2-amino-thiazole-4-carboxylic acid dimethylamide as a yellow gum which was used without further purification (0.14 g, 86%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07427635B2
Source datasetuspto-grants-2008_09
ORD IDord-59b9142b2dfd4e709574f6b0fc9ce70e
Source noteuspto-grants-2008_09