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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 512542Generated: October 27, 2026

N-bromobutanimide → Ethyl 5-amino-2-bromothiazole-4-carboxylate

https://huagongshe.com/reaction/512542

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantEthyl 5-amino-1,3-thiazole-4-carboxylateHCID 12620181—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductEthyl 5-amino-2-bromothiazole-4-carboxylateHCID 5935580158.2%

Reaction Steps

N-Bromosuccinimide (0.54 g, 3.03 mmol) was added to a solution of 5-aminothiazole-4-carboxylic acid ethyl ester (0.44 g, 2.53 mmol) [prepared according to the procedure described by Golankiewicz et al. (Tetrahedron, 41 (24), 5989-5994 (1985))] in acetonitrile (10 mL), and the mixture was stirred for 30 min. The reaction mixture was diluted with EtOAc (50 mL) and washed with 5% K2CO3 aq. solution (25 mL) followed by brine (25mL). The organic layer was dried over Na2SO4 and concentrated. The residue was purified by silica gel column chromatography eluted with 15% EtOAc in hexane to give 0.37 g (58% yield) of the titled compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09102637B2
Source datasetuspto-grants-2015_08
ORD IDord-939b78f90ce94b139a36b81af49567f9
Source noteuspto-grants-2015_08