Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 86715506 | HCID 86715506 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86715505 | HCID 86715505 | 94.1% |
Reaction Steps
2′-(4-Fluoro-3-methylphenyl)-[3,3′-bipyridine]-6-carbonitrile (2.2 g), Pd/C (0.4 g) and conc. HCl (3 mL) in EtOH (100 mL) was hydrogenated in a par shaker at 40 psi overnight. The reaction mixture was filtered through Celite® and concentrated. The concentrate was treated with CH2Cl2 (120 mL) and sat. aq. NaHCO3 (25 mL). Organic layer was separated and the aqueous layer was re-extracted with CH2Cl2 (2×50 ml). Combined organic layers were stirred over anhydrous Na2SO4 for 30 min, filtered, concentrated and dried under high vacuum to obtain thick viscous liquid of (2′-(4-Fluoro-3-methylphenyl)-[3,3′-bipyridin]-6-yl)methanamine (2.1 g, purity 97%). 1H NMR (300 MHz, DMSO-d6): δ 8.66 (dd, J=4.7, 1.6 Hz, 1H), 8.26 (s, 1H), 7.86 (d, J=1.6 Hz, 1H), 7.54 (dd, J=8.0, 2.2 Hz, 1H), 7.48 (dd, J=7.7, 4.8 Hz, 1H), 7.37 (d, J=8.1 Hz, 1H), 7.32 (d, J=8.0 Hz, 1H), 6.97 (dd, J=6.9, 1.5 Hz, 2H), 3.78 (s, 2H), 2.58 (br s, 2H), 2.16 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09145433B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-ec9ff9f6a4664a74becad63101002980 |
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| Source note | uspto-grants-2015_09 |
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