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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2380636Generated: November 3, 2026

Ethanol → 2-Amino-5-(3-pyridylsulfinyl)thiazole

https://huagongshe.com/reaction/2380636

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 15729196HCID 15729196—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
Product2-Amino-5-(3-pyridylsulfinyl)thiazoleHCID 1572919737.2%

Reaction Steps

To a mixture of 2-amino-5-(3-pyridylthio)thiazole (3.0 g) in a mixture of dichloromethane (100 ml) and chloroform (100 ml) was added dropwise the solution of 3-chloroperbenzoic acid (3.4 g) in dichloromethane (50 ml) at 5° C. with stirring. The mixture was stirred at 5° C. for hours. The reaction mixture was washed with aqueous sodium bicarbonate and the aqueous layer was extracted with a mixture of tetrahydrofuran and ethyl acetate (1:1), washed with aqueous saturated sodium chloride and dried over magnesium sulfate. The solvent was concentrated under reduced pressure and the residue was recrystallized from ethanol no give 2-amino-5-(3-pyridylsulfinyl)thiazole (1.2 g, yield: 37.2%). mp: 178°-179° C. IR (Nujol): 3300, 3150, 1630, 1580, 1520, 1485, 1325, 1220 cm-1NMR (DMSO-d6, 200 MHZ, ppm): 7.58-7.70 (1H, m), 7.80 (1H, s), 8.00 (2H, s), 7.98-8.05 (1H, m), 8.72 (2H, br s) Mass: M+1 226, M 225, m/e 209, 177, 147

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05369107
Source datasetuspto-grants-1994_11
ORD IDord-475d9d535bd9456aa3c335e82a5362b3
Source noteuspto-grants-1994_11