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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2389799Generated: October 30, 2026

N-bromobutanimide → 3-Bromo-5-chloro-7-(2,4-dichlorophenyl)imidazo[1,2-c]pyrimidine

https://huagongshe.com/reaction/2389799

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 59312932HCID 59312932—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
SolventEthyl AcetateHCID 8857—
Product3-Bromo-5-chloro-7-(2,4-dichlorophenyl)imidazo[1,2-c]pyrimidineHCID 59312920—

Reaction Steps

200 mg (0.67 mmol) of 5-chloro-7-(2,4-dichlorophenyl)imidazo[1,2-c]pyrimidine (Example 6A) are suspended in chloroform (30 ml), 238 mg (1.34 mmol) of N-bromosuccinimide are added, and the reaction mixture is stirred at RT for 12 h. The reaction mixture is diluted with ethyl acetate (100 ml) and water (75 ml), and the organic phase is separated off, dried over magnesium sulphate and concentrated in a rotary evaporator. The residue is stirred with acetonitrile (20 ml) and then diethyl ether (20 ml), and the solid is filtered off with suction and dried. 103 mg (41% of theory) of the product are isolated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273752B2
Source datasetuspto-grants-2012_09
ORD IDord-7ca71292a5c1434194b379263f8ac049
Source noteuspto-grants-2012_09