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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1603439Generated: October 29, 2026

2-Ethoxycarbonyl-3-methylimidazo[5,1-b]thiazole → {3-Methylimidazo[4,3-b][1,3]thiazol-2-yl}methanol

https://huagongshe.com/reaction/1603439

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Ethoxycarbonyl-3-methylimidazo[5,1-b]thiazoleHCID 19605133—
ReactantHCID 178418435HCID 178418435—
SolventEthanolHCID 702—
Product{3-Methylimidazo[4,3-b][1,3]thiazol-2-yl}methanolHCID 1960513498.7%

Reaction Steps

A 1.56 g portion of sodium boron hydride was added to 60 ml of an ethanol solution containing 1.684 g of 2-ethoxycarbonyl-3-methylimidazo[5,1-b]thiazole, and the mixture was then stirred at room temperature for 4 days. The solvent was evaporated under reduced pressure, and water was then added thereto. The solution was extracted twice with dichloromethane, and the combined organic layer was dried over anhydrous magnesium sulfate and then filtered. Afterward, the solvent was evaporated under reduced pressure to obtain 1.33 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05990101
Source datasetuspto-grants-1999_11
ORD IDord-6282f628573d4a6e9f3f2186f4bb343a
Source noteuspto-grants-1999_11