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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1984630Generated: November 1, 2026

Benzoyl Peroxide → 6-(4-{[4-(4-amino-1H-pyrazolo[3,4-d]pyrimidin-1-yl)piperidin-1-yl]methyl}phenyl)-2-chloro-5-phenylnicotinonitrile

https://huagongshe.com/reaction/1984630

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Chloro-6-(4-methylphenyl)-5-phenylnicotinonitrileHCID 21103198—
Reactant1-piperidin-4-yl-1H-pyrazolo[3,4-d]pyrimidin-4-amineHCID 57713946—
SolventChloroformHCID 6212—
Product6-(4-{[4-(4-amino-1H-pyrazolo[3,4-d]pyrimidin-1-yl)piperidin-1-yl]methyl}phenyl)-2-chloro-5-phenylnicotinonitrileHCID 11443807—

Reaction Steps

A mixture of 2-chloro-6-(4-methylphenyl)-5-phenylnicotinonitrile (4-4) (0.204 g, 0.67 mmol), NBS (0.125 g, 0.70 mmol) and benzoylperoxide (0.032 g, 0.13 mmol) in chloroform (5 mL) was heated to reflux for 24 h. Concentrated in vacuo and the residue was dissolved in MeOH (15 mL) and THF (15 mL). To this solution was added 1-piperidin-4-yl-1H-pyrazolo[3,4-d]pyrimidin-4-amine (0.146 g, 0.67 mmol) and diisopropylethylamine (0.433 g, 3.35 mmol). The mixture was stirred overnight and concentrated. The residue was treated with Na2CO3 (20 mL, 2M) and extracted with CH2Cl2. The combined organic layers was dried, filtered and concentrated in vacuo. The solid was purified by silicon gel chromatography (2-4% MeOH in CH2Cl2) to give the title compound. LRMS m/z (M+H) Calcd: 522.03, found: 521.27.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07544677B2
Source datasetuspto-grants-2009_06
ORD IDord-73b7fdeadddd490d854246cf2eceb87e
Source noteuspto-grants-2009_06