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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2222995Generated: October 30, 2026

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

https://huagongshe.com/reaction/2222995

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 Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of (4-dimethylcarbamoyl-thiazol-2-yl)-carbamic acid tert-butyl ester (150 mg, 0.53 mmol) in dichloromethane (1 mL) at 0° C. was added trifluoroacetic acid (2.5 mL, 32 mmol) and the mixture stirred at 0° C. until all of the starting material had been consumed. The reaction mixture was concentrated in vacuo, the residue dissolved in ethyl acetate, washed with saturated aqueous sodium bicarbonate (2×), brine, dried over sodium sulfate and concentrated in vacuo to give crude 2-amino-thiazole-4-carboxylic acid dimethylamide as a viscous colorless oil which was used without further purification (85 mg, 90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07371869B2
Source datasetuspto-grants-2008_05
ORD IDord-ab1f620ec28c40f18aa42485c2e4a7cb
Source noteuspto-grants-2008_05