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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 869215Generated: November 2, 2026

Ethyl 2-aminothiazole-4-carboxylate → HCID 86686148, compound

https://huagongshe.com/reaction/869215

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-aminothiazole-4-carboxylateHCID 73216—
Reactant2-Bromo-1-(6-chloropyridazin-3-yl)ethanoneHCID 21702089—
SolventMethyl Ethyl KetoneHCID 6569—
ProductHCID 86686148HCID 8668614818%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a 20 dram vial was added 2-bromo-1-(6-chloropyridazin-3-yl)ethanone (4.2 g, 18 mmol), ethyl-2-aminothiazole-4-carboxylate (3.1 g, 18 mmol), and methylethylketone (40 mL). The mixture was heated to 90° C. and stirred overnight. The reaction was then concentrated and purified by silica gel chromatography (EtOAc/hex) to afford 1.0 g of ethyl 6-(6-chloropyridazin-3-yl)imidazo[2,1-b]thiazole-3-carboxylate as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969346B2
Source datasetuspto-grants-2015_03
ORD IDord-2849ec06eb4943c39e0c3f143f49ab6e
Source noteuspto-grants-2015_03