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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1924055Generated: November 2, 2026

Ethyl 2-aminothiazole-4-carboxylate → Ethyl 6-(2-nitrophenyl)imidazo[2,1-b]thiazole-3-carboxylate

https://huagongshe.com/reaction/1924055

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-aminothiazole-4-carboxylateHCID 73216—
Reactant2-Bromo-2'-nitroacetophenoneHCID 244025—
SolventMethyl Ethyl KetoneHCID 6569—
ProductEthyl 6-(2-nitrophenyl)imidazo[2,1-b]thiazole-3-carboxylateHCID 2523252279.4%

Reaction Steps

In a typical run, 2.1 g of ethyl 2-aminothiazole-4-carboxylate (Combi-Blocks, 0.0123 mol) was mixed with 25 mL of methyl ethyl ketone along with 2-bromo-2′-nitroacetophenone (3.0 g, 0.0123 mol). The reaction mixture was stirred under reflux for 18 hours. It was then cooled to room temperature and filtered to remove some of the solids. The filtrate was concentrated to afford 3.10 g of 6-(2-nitro-phenyl)-imidazo[2,1-b]thiazole-3-carboxylic acid ethyl ester (MS, M++H=318).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178536B2
Source datasetuspto-grants-2012_05
ORD IDord-6a2599daf7584689bbecc5d0af83fb71
Source noteuspto-grants-2012_05