Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2247338Generated: October 26, 2026

Water → N-[5-(4-Fluoro-3-methanesulfonyl-phenyl)-4-methyl-thiazol-2-yl]-acetamide

https://huagongshe.com/reaction/2247338

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
ReactantAcetylthioureaHCID 2723593—
ReactantHCID 85861733HCID 85861733—
SolventEthanolHCID 702—
ProductN-[5-(4-Fluoro-3-methanesulfonyl-phenyl)-4-methyl-thiazol-2-yl]-acetamideHCID 86598409—

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 1-bromo-1-(4-fluoro-3-methanesulfonyl-phenyl)-propan-2-one (Example 47c) (0.17 g, 0.55 mmol) and N-acetylthiourea (0.065 g, 0.55 mmol) in ethanol is heated at 70° C. for 3 hours then at room temperature over two days. The reaction mixture is poured into water (200 ml) and extracted with ethyl acetate (3×50 ml). The combined organic layers are dried over MgSO4, filtered and concentrated to afford a viscous solid. This solid in a minimum amount of ethyl acetate is sonicated to give a suspension which is then heated until all solid has dissolved then left to cool to room temperature overnight. The white crystalline solid is filtered off to afford the titled compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07687637B2
Source datasetuspto-grants-2010_03
ORD IDord-1fc0031df56645d3b1b04ebef8f49c84
Source noteuspto-grants-2010_03