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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1948414Generated: October 30, 2026

N-bromobutanimide → N-[5-(2-Bromo-thiophen-3-yl)-4-methyl-thiazol-2-yl]-acetamide

https://huagongshe.com/reaction/1948414

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantN-[4-methyl-5-(3-thienyl)-1,3-thiazol-2-yl]acetamideHCID 11993592—
SolventAcetonitrileHCID 6342—
ProductN-[5-(2-Bromo-thiophen-3-yl)-4-methyl-thiazol-2-yl]-acetamideHCID 8665243997%

Reaction Steps

N-[4-methyl-5-(3-thienyl)-1,3-thiazol-2-yl]acetamide obtained in Step I as described above (3880 mg; 16.3 mmol; 1 eq) is dissolved in ACN (375 ml). N-bromosuccinimide (2898 mg; 16.3 mmol; 1 eq) is added and the resulting solution is stirred at room temperature for 30 minutes. Solvents are concentrated. Water is added and the desired product is extracted with EtOAc (3 times). Organic phases are washed with water (3 times) and dried over MgSO4, affording the title compound (5000 mg; 97%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399497B2
Source datasetuspto-grants-2013_03
ORD IDord-76573bf97d3848dcbf81621ed2183f9c
Source noteuspto-grants-2013_03