Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1656990Generated: November 3, 2026

m-Chloroperbenzoic acid → 2-Amino-4-methyl-5-(2-pyridylsulfinyl)thiazole

https://huagongshe.com/reaction/1656990

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant2-Amino-4-methyl-5-(2-pyridylthio)thiazoleHCID 18954735—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
Product2-Amino-4-methyl-5-(2-pyridylsulfinyl)thiazoleHCID 1572918952.2%

Reaction Conditions

Temperature5 °C

Reaction Steps

A mixture of 2-amino-4-methyl-5-(2-pyridylthio)thiazole (1.7 g) and 3-chloroperbenzoic acid (1.8 g) in a mixture of chloroform (20 ml) and dichloromethane (50 ml) was stirred at 5° C. for 3.5 hours. The reaction mixture was washed with aqueous sodium bicarbonate and dried over magnesium sulfate. The solvent was concentrated under reduced pressure to give solid. The solid was subjected to column chromatography on silica gel (silica gel 60, 70-230 mesh; Merck: 100 g) and eluted with a mixture of chloroform and methanol (10:1). The fractions containing the objective compound were combined and concentrated under reduced pressure to give 2-amino-4-methyl-5-(2-pyridylsulfinyl)thiazole (0.95 g, yield: 52.2 %). mp: 190°-193° C. (dec.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05256675
Source datasetuspto-grants-1993_10
ORD IDord-3d40e69cefd048dc94fa9772c97cb315
Source noteuspto-grants-1993_10