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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376596Generated: October 30, 2026

Pyridine → 5-(Acetylamino)methylimidazo[5,1-b]thiazole

https://huagongshe.com/reaction/1376596

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetic AnhydrideHCID 7918—
Reactant5-Aminomethylimidazo[5,1-b]thiazoleHCID 21262358—
SolventDichloromethaneHCID 6344—
Product5-(Acetylamino)methylimidazo[5,1-b]thiazoleHCID 2291669983%

Reaction Steps

To a solution of 150 mg (0.98 mmol) of 5-aminomethylimidazo[5,1-b]thiazole in 1 ml of methylene chloride were added 1 ml of acetic anhydride and 0.5 ml of pyridine, and the mixture was stirred overnight at room temperature. The reaction solution was concentrated. The residue was dissolved in methylene chloride, and washed with water. The organic layer was dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by flash column chromatography using silica gel, eluting with ethyl acetate to give 159 mg (yield 83%) of the title compound as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05663162
Source datasetuspto-grants-1997_09
ORD IDord-e108199616c24ebc956c7e61c3bed672
Source noteuspto-grants-1997_09