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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-Chloro-6-(4-methylphenyl)-5-phenylnicotinonitrile | HCID 21103198 | — |
| Reactant | 1-piperidin-4-yl-1H-pyrazolo[3,4-d]pyrimidin-4-amine | HCID 57713946 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 6-(4-{[4-(4-amino-1H-pyrazolo[3,4-d]pyrimidin-1-yl)piperidin-1-yl]methyl}phenyl)-2-chloro-5-phenylnicotinonitrile | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07544677B2 |
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| Source dataset | uspto-grants-2009_06 |
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| ORD ID | ord-73b7fdeadddd490d854246cf2eceb87e |
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| Source note | uspto-grants-2009_06 |
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