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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1656974Generated: November 1, 2026

Hydrochloric Acid → 2-Amino-4-(4-aminophenylthiomethyl)-5-chlorothiazole

https://huagongshe.com/reaction/1656974

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
Reactant5-Chloro-2-formylamino-4-(4-formylaminophenylthiomethyl)thiazoleHCID 15729173—
SolventTetrahydrofuranHCID 8028—
Product2-Amino-4-(4-aminophenylthiomethyl)-5-chlorothiazoleHCID 1572917479.3%

Reaction Steps

A solution of 5-chloro-2-formylamino-4-(4-formylaminophenylthiomethyl)thiazole (3.5 g) in a mixture of concentrated hydrochloric acid (9 ml), methanol (30 ml) and tetrahydrofuran (30 ml) was stirred at room temperature for 4 hours. The reaction mixture was concentrated under reduced pressure and the residue was dissolved in water. The solution was adjusted to pH 8 using aqueous sodium bicarbonate with stirring under ice cooling. The precipitates were collected by filtration, washed with water and dried in vacuo to give solid. The solid was subjected to column chromatography on silica gel (silica gel 60, 70-230 mesh; Merck: 150 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-(4-aminophenylthiomethyl)-5-chlorothiazole (2.3 g, yield: 79.3%). mp: 158°-163° C. (dec.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05256675
Source datasetuspto-grants-1993_10
ORD IDord-aa39f29088174ab4a6969784ff25c440
Source noteuspto-grants-1993_10