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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1192349Generated: October 29, 2026

N-bromobutanimide → 3-Bromo-4-chloro-1H-pyrazolo[3,4-d]pyrimidine

https://huagongshe.com/reaction/1192349

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant4-Chloro-1H-pyrazolo[3,4-d]pyrimidineHCID 221095—
SolventChloroformHCID 6212—
Product3-Bromo-4-chloro-1H-pyrazolo[3,4-d]pyrimidineHCID 17847839477%

Reaction Steps

To a suspension of 4-Chloro-1H-pyrazolo[3,4-d]pyrimidine (1.1 g, 7.1 mmol) in CHCl3 (50 mL) was added NBS (1.49 g, 8.4 mmol) The mixture was stirred at room temperature for 5 hours, cooled to 0 C and the solids were isolated by vacuum filtration, rinsed with cold CHCl3, and air dried. The solid was purified by column chromatography on silica (50% EtOAc/hexanes) to give 3-Bromo-4-chloro-1H-pyrazolo[3,4-d]pyrimidine (1.3, 77%.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680114B2
Source datasetuspto-grants-2014_03
ORD IDord-d0623c7ee410495b94715e0a64356ee4
Source noteuspto-grants-2014_03