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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1878528Generated: October 25, 2026

N-bromobutanimide → 3-Bromo-5-chloro-7-morpholin-4-yl-pyrazolo[1,5-a]pyrimidine

https://huagongshe.com/reaction/1878528

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant5-Chloro-7-morpholin-4-yl-pyrazolo[1,5-a]pyrimidineHCID 58531071—
SolventDichloromethaneHCID 6344—
SolventSodium BicarbonateHCID 516892—
Product3-Bromo-5-chloro-7-morpholin-4-yl-pyrazolo[1,5-a]pyrimidineHCID 5853100361%

Reaction Steps

There was dissolved, in methylene chloride (2 mL), 5-chloro-7-morpholin-4-yl-pyrazolo[1,5-a]pyrimidine (100 mg, 0.419 mM), then N-bromo-succinimide (78.8 mg, 0.443 mM) was added to the solution and the mixture was stirred at room temperature for one hour. This reaction liquid was diluted with a saturated aqueous sodium bicarbonate solution and then extracted with ethyl acetate. The extracts thus obtained were combined, dried over anhydrous sodium sulfate and the solvent was then distilled off. The resulting residue was purified by the silica gel column chromatography (methylene chloride) to thus give the title compound (80.7 mg, yield: 61%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08314098B2
Source datasetuspto-grants-2012_11
ORD IDord-2068f934617a4756a3adfe7cbbc13970
Source noteuspto-grants-2012_11