Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 3-Bromopyridine | HCID 12286 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Dibenzylidene acetone | HCID 95417 | — |
| Reactant | 2-(1H-pyrazol-4-yl)pyridine | HCID 3578981 | — |
| Catalyst | copper(II) trifluoromethanesulfonate | HCID 2734996 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 10171371 | HCID 10171371 | — |
Reaction Steps
2-(1H-Pyrazol-4-yl)pyridine (292 mg, 2 mmol), 3-bromopyridine (0.23 mL, 2.4 mmol), Cu(OTf)2 (50 mg, 0.1 mmol), dibenzylideneacetone (24 mg, 0.1 mmol), Cs2CO3 (780 mg, 2.4 mmol) and 1,10-phenanthracene (360 mg, 2.4 mmol) in dry o-xylene (1.5 mL) under Ar (g) were heated at 115° C. for 18 h. After cooling to ambient temperature, NH4Cl (20 mL) and dichloromethane (20 mL) were added and the reaction mixture shaken, the dichloromethane layer was separated and the aqueous layer shaken with dichloromethane (2×20 mL). The combined organic layers were dried over Na2SO4 and concentrated in vacuo to a brown oil. This was purified by liquid chromatography on silica gel eluting with EtOAc to give a solid that was further purified by HPLC to afford 2-(1-pyridin-3-yl-1H-pyrazol-4-yl)pyridine. 1H NMR (CD3Cl, 300 MHz) δ 9.08 (1H, d), 8.58-8.64 (2H, m), 8.56 (1H, s), 8.24 (1H, s), 8.12 (1H, ddd), 7.73 (1H, ddd), 7.56-7.59 (1H, m), 7.45 (1H, dd), 7.19 (1H, ddd). MS (ESI) 223 (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-2eddc24c364b4326af59546f1700e594 |
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| Source note | uspto-grants-2009_08 |
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