Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 45270Generated: October 26, 2026

5-[(2-Chlorophenyl)carbonyl]-1,3-thiazol-2-amine → Ethanone, 1-(2-chlorophenyl)-

https://huagongshe.com/reaction/45270

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-[(2-Chlorophenyl)carbonyl]-1,3-thiazol-2-amineHCID 57456943—
ReactantN'-[5-(2-chloro-benzoyl)-thiazol-2-yl]-N,N-dimethyl-formamidineHCID 66628633—
SolventHydrochloric AcidHCID 313—
ProductEthanone, 1-(2-chlorophenyl)-HCID 72864—
Product5-[(2-Chlorophenyl)carbonyl]-1,3-thiazol-2-amineHCID 57456943—

Reaction Conditions

Temperature70 °C

Reaction Steps

(2-Amino-thiazol-5-yl)-(2-chloro-phenyl)-methanone The crude N′-[5-(2-chloro-benzoyl)-thiazol-2-yl]-N,N-dimethyl-formamidine was dissolved in 10% hydrochloric acid (150 mL) and heated at 70° C. for 4 hours. The precipitate was filtered, washed with ether, and then suspended in a 10% sodium carbonate solution (250 mL). The suspension was stirred for 1 hour and the precipitate was filtered, washed with ether, and dried in air to give (2-amino-thiazol-5-yl)-(2-chloro-phenyl)-methanone as a brown solid (8.5 g, 36 mmol, 55% from 1-(2-chloro-phenyl)-ethanone). ESI-MS m/z calc. 238.0. found 239.3 (M+1)+1; 1H NMR (DMSO) δ 7.25 (s, 1H), 7.42-7.55 (m, 4H), 8.35 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541453B2
Source datasetuspto-grants-2013_09
ORD IDord-daa927d7ed8f4ad086825775a4ad1448
Source noteuspto-grants-2013_09