HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-(4-Aminopiperidin-1-yl)pyridine-3-carbonitrile → HCID 53327813, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-(4-Aminopiperidin-1-yl)pyridine-3-carbonitrile | HCID 18768671 | — |
| Reactant | 3-(5-(Trifluoromethyl)-1,2,4-oxadiazol-3-yl)benzoic acid | HCID 25180854 | — |
| Product | HCID 53327813 | HCID 53327813 | 41% |
Reaction Steps
This compound was synthesized from 6-(4-aminopiperidin-1-yl)nicotinonitrile and 3-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)benzoic acid as described for example 37 step 3 (70 mg, yield 41%). 1H NMR (400 MHz, CDCl3) δ 8.42 (m, 2H), 8.27 (d, J=7.8 Hz, 1H), 8.04 (d, J=7.8 Hz, 1H), 7.66-7.61 (m, 2H), 6.67 (d, J=9.0 Hz, 1H), 6.14 (d, J=7.8 Hz, 1H), 4.51-4.48 (m, 2H), 4.39-4.29 (m, 1H), 3.20-3.13 (m, 2H), 2.24-2.20 (dd, J=12.3 Hz, 2.3 Hz, 2H), 1.62-1.52 (m, 2H). MS (ESI) m/z: Calculated for C21H17F3N6O2: 442.14. found: 443.2 (M+H)+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08981084B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-220f8f189b9a43de99b11809a79d5a07 |
| Source note | uspto-grants-2015_03 |