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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 586378Generated: October 29, 2026

Hydrochloric Acid → 5-Ethyl-6-hydroxymethyl-imidazo[2,1-b]thiazole

https://huagongshe.com/reaction/586378

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 20825691HCID 20825691—
ReactantDiisobutylaluminumhydrideHCID 21225700—
SolventTetrahydrofuranHCID 8028—
Product5-Ethyl-6-hydroxymethyl-imidazo[2,1-b]thiazoleHCID 22335122—

Reaction Steps

Diisobutylaluminum hydride (1M in THF, 11 mL, 11 mmol) is added to a solution of 5-ethyl-imidazo[2,1-b]thiazole-6-carboxylic acid ethyl ester (800 mg, 3.6 mmol) in THF (20 mL). The mixture is stirred at room temperature for 0.5 h. HCl (10%, 2 mL) is added, and the mixture is stirred for an additional 5 min. The mixture is neutralized by the addition of sodium hydroxide (2 N) until pH is above 10 and then extracted with ethyl acetate (3×20 mL). The combined organic layers are dried and solvent removed to give 5-ethyl-6-hydroxymethyl-imidazo[2,1-b]thiazole as a solid. Step 3. Preparation of 6-chloromethyl-5-ethyl-imidazo[2,1-b]thiazole

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06936617B2
Source datasetuspto-grants-2005_08
ORD IDord-256fb4f67cf74c71abe1da9f139d0d3a
Source noteuspto-grants-2005_08