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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1185253Generated: October 30, 2026

N-bromobutanimide → 2-Bromo-5-((tert-butoxycarbonyl)amino)thiazole-4-carboxylic acid

https://huagongshe.com/reaction/1185253

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant5-(Boc-amino)-thiazole-4-carboxylic acidHCID 58182203—
SolventDichloromethaneHCID 6344—
Product2-Bromo-5-((tert-butoxycarbonyl)amino)thiazole-4-carboxylic acidHCID 5818215670%

Reaction Steps

To a solution of 5-(tert-butoxycarbonylamino)thiazole-4-carboxylic acid (1.72 g, 10 mmol) in DCM (50 mL) was added in three portions NBS (1.95 g, 11 mmol); the reaction mixture was stirred at ambient temperature for 1 h. Reaction was concentrated in vacuo; resulted residue was purified by silica gel column chromatography (6:1 Pet-ether-EtOAc) to afford 2-bromo-5-(tert-butoxycarbonylamino)thiazole-4-carboxylic acid (1.75 g, 70%) as white solid: 1H-NMR (CDCl3, 500 MHz) δ (ppm): 13.65 (s, 1H), 10.03 (s, 1H), 1.49 (s, 9H). MS (ESI) m/z: 324 [M+H+]

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08669361B2
Source datasetuspto-grants-2014_03
ORD IDord-84d8aca1337f4554b976a9a8612e4fb0
Source noteuspto-grants-2014_03