Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 127104Generated: October 31, 2026

Pyridine → Ethyl {2-[(methanesulfonyl)amino]-1,3-thiazol-5-yl}acetate

https://huagongshe.com/reaction/127104

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantEthyl 2-(2-aminothiazol-5-yl)acetateHCID 717815—
SolventDichloromethaneHCID 6344—
ProductEthyl {2-[(methanesulfonyl)amino]-1,3-thiazol-5-yl}acetateHCID 2028865260.1%

Reaction Steps

To a solution of ethyl 2-aminothiazol-5-ylacetate (32 g.) in methylene chloride (160 ml.) was added pyridine (27.2 g.) under ice-cooling, and to the mixture was dropwise added mesyl chloride (29.6 g.) in methylene chloride (29.6 ml.) over 30 minutes at 8° to 10° C. The mixture was further stirred for 8 hours at room temperature. After the reaction, methylene chloride was distilled off from the reaction mixture, and to the residue were added water (300 ml.) and ethyl acetate (300 ml.). The resulting mixture was adjusted to pH 2 with 10% hydrochloric acid under ice-cooling, and the precipitates were collected by filtration and washed with ethyl acetate. The precipitates were recrystallized from ethanol (600 ml.) to give ethyl 2-methanesulfonamidothiazol-5-ylacetate (27.3 g.), mp 153° to 155° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04254260
Source datasetuspto-grants-1981_03
ORD IDord-3dad1036b9dd452d961c4d42bc138ca6
Source noteuspto-grants-1981_03