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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2171538Generated: November 1, 2026

Chlorosuccinimide → 3,5-Dichloro-7-(2,4-dichlorophenyl)imidazo[1,2-c]pyrimidine

https://huagongshe.com/reaction/2171538

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
ReactantHCID 59312932HCID 59312932—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
SolventEthyl AcetateHCID 8857—
Product3,5-Dichloro-7-(2,4-dichlorophenyl)imidazo[1,2-c]pyrimidineHCID 59312902—

Reaction Steps

300 mg (1.0 mmol) of 5-chloro-7-(2,4-dichlorophenyl)imidazo[1,2-c]pyrimidine (Example 6A) are suspended in chloroform (15 ml), 240 mg (1.8 mmol) of N-chlorosuccinimide 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 diethyl ether (20 ml), and the solid is filtered off with suction and dried. 63 mg (18% of theory) of the product are isolated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051323B2
Source datasetuspto-grants-2015_06
ORD IDord-bcbf8ff6dbe842a0a34b7f00872751fc
Source noteuspto-grants-2015_06