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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1656963Generated: October 31, 2026

Methanesulfonyl chloride → HCID 15729162, compound

https://huagongshe.com/reaction/1656963

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 15729149HCID 15729149—
SolventPyridineHCID 1049—
ProductHCID 15729162HCID 1572916296.6%

Reaction Steps

A solution of 2-acetamido-5-(4-aminophenylthio)thiazole (3.2 g) in pyridine (64 ml) was added methanesulfonyl chloride (1.52 g) at 5° C. with stirring. The reaction mixture was stirred for 3 hours at 5° C. and concentrated in vacuo to give solid. The solid was subject to column chromatography on silica gel (silica gel, 70-230 mesh; Merck: 200 g) and eluted with a mixture of chloroform and methanol (50:1) and eluted with a mixture of chloroform and methanol (20:1). The fractions containing the objective compound were combined and evaporated to dryness in vacuo to give 2-acetamido-5-(4-methanesulfonylaminophenylthio)thiazole (4.0 g, yield: 96.6%). mp: 236°-239° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05256675
Source datasetuspto-grants-1993_10
ORD IDord-d6ff0ffdfe644ecd9558d1e43f67e1dc
Source noteuspto-grants-1993_10