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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1360873Generated: October 31, 2026

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

https://huagongshe.com/reaction/1360873

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 numberUS07879888B2
Source datasetuspto-grants-2011_02
ORD IDord-4cc5c5d4d6264d5fbcc18c1d7c84900b
Source noteuspto-grants-2011_02