Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2380629Generated: November 2, 2026

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

https://huagongshe.com/reaction/2380629

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 %).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05369107
Source datasetuspto-grants-1994_11
ORD IDord-020948dd777c4650bb562ad95bcb2066
Source noteuspto-grants-1994_11