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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2380615Generated: November 3, 2026

Chloroform → 2-Acetylamino-4-hydroxymethyl-5-(4-pyridylthio)thiazole

https://huagongshe.com/reaction/2380615

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 15729141HCID 15729141—
Reactantpyridine-4-thiolHCID 178418431—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
Product2-Acetylamino-4-hydroxymethyl-5-(4-pyridylthio)thiazoleHCID 1572917566.1%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 2-acetylamino-5-chloro-4-hydroxymethylthiazole (1 g), 4-mercaptopyridine (0.6 g) and potassium carbonate (1 g) in N,N-dimethylformamide (20 ml) was heated at 110° C. for 8 hours with stirring. The reaction mixture was poured into ice water and filtered by suction. The filtrate was extracted with a mixture of ethyl acetate and tetrahydrofuran (1:1) 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: 75 g) and eluded with a mixture of chloroform and methanol (10:1l). The fractions containing the objective compound were combined and concentrated under reduced pressure to give 2-acetylamino-4-hydroxymethyl-5-(4-pyridylthio)thiazole (0.90 g, yield: 64.3%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05369107
Source datasetuspto-grants-1994_11
ORD IDord-d97fec0c4fcd4f7e93656454d16be66c
Source noteuspto-grants-1994_11