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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 644433Generated: October 29, 2026

N-bromobutanimide → 2-Acetoxy-5-bromo-N-(5-bromo-4-[(1,1-dimethyl)ethyl]thiazol-2-yl)benzamide

https://huagongshe.com/reaction/644433

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantAcetoxy-5-bromo-N-{4-[(1,1-dimethyl)ethyl]thiazol-2-yl}benzamideHCID 85823490—
SolventAcetonitrileHCID 6342—
Product2-Acetoxy-5-bromo-N-(5-bromo-4-[(1,1-dimethyl)ethyl]thiazol-2-yl)benzamideHCID 86602679—

Reaction Steps

2-Acetoxy-5-bromo-N-{4-[(1,1-dimethyl)ethyl]thiazol-2-yl}benzamide (compound of Example 181(2); 0.20 g, 0.50 mmol) was dissolved in acetonitrile (10 mL). N-Bromosuccinimide (97.9 mg, 0.55 mmol) was added, and the mixture was stirred at room temperature for 1 hour. The reaction mixture was concentrated under reduced pressure, and the obtained residue was purified by chromatography on silica gel (n-hexane:ethyl acetate=3:1) to give the title compound as a crude product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700655B2
Source datasetuspto-grants-2010_04
ORD IDord-0fc3733fe9bb456ca51e5d34f47c9cee
Source noteuspto-grants-2010_04