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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1446669Generated: October 31, 2026

N-bromobutanimide → 3-Bromo-7-thiazol-2-yl-imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/1446669

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant7-Thiazol-2-yl-imidazo[1,2-a]pyridineHCID 68543434—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
Product3-Bromo-7-thiazol-2-yl-imidazo[1,2-a]pyridineHCID 6853978767.5%

Reaction Steps

Dissolve 7-thiazol-2-yl-imidazo[1,2-a]pyridine (1.14 g, 5.66 mmol) in 25 mL absolute ethanol, then add NBS (1.0 g, 5.66 mmol), stir the mixture at room temperature for 15 minutes, dilute with 35 mL dichloromethane and apply to a 10 g SCX Mega Bond-Elut™ cartridge (Varian) pre-washed with 150 mL 1:1 CH2Cl2:MeOH. Wash the SCX cartridge with 300 mL 1:1 CH2Cl2:MeOH, elute with 150 mL CH2Cl2:2 M NH3-MeOH, and concentrate the eluates and dry to provide 1.07 g (67%) of the title compound as a tan solid. MS (ES) 280, 282.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07666879B2
Source datasetuspto-grants-2010_02
ORD IDord-21a2d8e681ab4c06a3299f810d10953b
Source noteuspto-grants-2010_02