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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2171537Generated: November 1, 2026

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

https://huagongshe.com/reaction/2171537

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 numberUS09051323B2
Source datasetuspto-grants-2015_06
ORD IDord-9f01aeb199d1497b985e5b479aa23167
Source noteuspto-grants-2015_06