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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 570140Generated: October 30, 2026

Water → 3-Bromo-2-(4-fluorophenyl)pyrazolo[1,5-a]pyrimidine

https://huagongshe.com/reaction/570140

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantN-bromobutanimideHCID 67184—
Reactant2-(4-Fluorophenyl)pyrazolo[1,5-a]pyrimidineHCID 69297261—
SolventChloroformHCID 6212—
Product3-Bromo-2-(4-fluorophenyl)pyrazolo[1,5-a]pyrimidineHCID 8374743876.1%

Reaction Steps

To a solution of 2-(4-fluorophenyl)pyrazolo[1,5-a]pyrimidine (5.8 g, 0.027 mol) in chloroform (60 mL) is added, at 0° C., N-bromosuccinimide (4.8 g, 0.027 mol). The mixture is stirred at room temperature for 1 h 30. The reaction mixture is then poured into water and extracted with dichloromethane (3×100 mL). The organic layer is dried over anhydrous magnesium sulphate, filtered and concentrated under reduced pressure. The crude material is filtered through a short pad of silica. 6 g (75%) of 3-bromo-2-(4-fluorophenyl)pyrazolo[1,5-a]pyrimidine are obtained as a brown solid which is used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09023844B2
Source datasetuspto-grants-2015_05
ORD IDord-283af891170a41819dfe6340dae04fa3
Source noteuspto-grants-2015_05