HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 594969Generated: October 30, 2026
Pyridine → 6-chloro-1-phenyl-1H-pyrazolo[3,4-d]pyrimidine
https://huagongshe.com/reaction/594969
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Reactant | 6-chloro-1H-pyrazolo[3,4-d]pyrimidine | HCID 52911254 | — |
| Catalyst | Cupric acetate | HCID 8895 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-chloro-1-phenyl-1H-pyrazolo[3,4-d]pyrimidine | HCID 86671732 | 92% |
Reaction Steps
A suspension of 6-chloro-1H-pyrazolo[3,4-d]pyrimidine (100 mg, 0.65 mmol), benzene boronic acid (1.5 eq), copper acetate (2 eq) and pyridine (2 eq) in dichloromethane (2 mL) was heated in the microwave at 80° C. for 15 min. After cooling to rt, the mixture was filtered and the resulting filtrate concentrated to give 6-chloro-1-phenyl-1H-pyrazolo[3,4-d]pyrimidine as a green oil (138 mg, 92%) which was used without further purification in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09242987B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-e4aa367686824dffbfc63ea3ff3f1d91 |
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| Source note | uspto-grants-2016_01 |
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