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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 362255Generated: October 26, 2026

Ethanol → 3-(Benzo[b]thiophen-3-yl)-5,6-dihydroimidazo[2,1-b]thiazole monohydrobromide

https://huagongshe.com/reaction/362255

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantEthylenethioureaHCID 2723650—
Reactant1-(1-Benzothiophen-3-yl)-2-bromoethan-1-oneHCID 2776341—
SolventAcetic AcidHCID 176—
Product3-(Benzo[b]thiophen-3-yl)-5,6-dihydroimidazo[2,1-b]thiazole monohydrobromideHCID 5107198487.3%

Reaction Steps

A mixture of 3-(2-bromoacetyl)benzo[b]thiophen (10.0 g), 2-imidazolidinethione (4.0 g), ethanol (120 ml) and acetic acid (80 ml) was heated under reflux for 24 hours then allowed to cool to ambient temperature. The resulting solid was collected by filtration and dried in vacuo at ambient temperature to give 3-(benzo[b]thiophen-3-yl)-5,6-dihydroimidazo[2,1-b]thiazole monohydrobromide 1.8 hydrate as a white solid (11.6 g), m.p. 227°-229° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05869492
Source datasetuspto-grants-1999_02
ORD IDord-4f580d759c6347298f2ae97b8ee1ba13
Source noteuspto-grants-1999_02