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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1667004Generated: October 31, 2026

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

https://huagongshe.com/reaction/1667004

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 numberUS08044198B2
Source datasetuspto-grants-2011_10
ORD IDord-d2a973c6d6ac4b0ab7e483a73c6cdf4c
Source noteuspto-grants-2011_10