Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 1-Naphthaleneboronic acid | HCID 254532 | — |
| Reactant | 2-(1H-pyrazol-4-yl)pyridine | HCID 3578981 | — |
| Catalyst | Cupric acetate | HCID 8895 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 10308203 | HCID 10308203 | — |
Reaction Steps
To 2-(1H-pyrazol-4-yl)pyridine (292 mg, 2 mmol), 1-napthaleneboronic acid (690 mg, 4 mmol), Cu(OAc)2 (547 mg, 3 mmol) and pyridine (0.32 mL, 4 mmol) in dichloromethane (4 mL) was added 0.5 g of 4 Å molecular sieves. The resulting reaction mixture was stirred at ambient temperature under atmospheric conditions for 48 h, whereupon it was filtered through Celite, washing with dichloromethane. The reaction mixture was concentrated on to silica gel in vacuo and purified by liquid chromatography onto silica gel eluting with EtOAc:hex (2:8 to 3:7) to afford 2-[1-(1-naphthyl)-1H-pyrazol-4-yl]pyridine as a white solid. 1H NMR (CD3Cl, 300 MHz) δ 8.63-8.65 (1H, m), 8.39 (1H, s), 8.34 (1H, s), 7.94-7.99 (3H, m), 7.73 (1H, ddd), 7.53-7.64 (5H, m), 7.18 (1H, m). MS (ESI) 272 (M+H)+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07569592B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-9e9b0df7f65a4304a72b4a5dee9b829a |
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| Source note | uspto-grants-2009_08 |
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