HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Amino-5-cyanopyridine → HCID 67482521, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Amino-5-cyanopyridine | HCID 818260 | — |
| Reactant | HCID 16058694 | HCID 16058694 | — |
| Product | HCID 67482521 | HCID 67482521 | — |
Reaction Steps
The product from Example 1, Part C (160 mg, 0.5 mmol) and 6-aminonicotinonitrile (89 mg, 0.75 mmol) were reacted as described in Example 5. After evaporation of the reaction solvent the residue was partitioned between water and EtOAc, the aqueous phase was washed with EtOAc. The combined organics were washed with brine, dried (Na2SO4), filtered, and evaporated. The title compound was obtained by silica gel chromatography (30 mg, 14%). 1H NMR (400 MHz, CDCl3) δ 8.84 (br s, 1H), 8.55 (d, J=2 Hz, 1H), 8.30 (d, J=9 Hz, 1H), 7.95 (dd, J=9 Hz, 2 Hz, 1H), 7.21 (d, J=9 Hz, 2H), 6.83 (d, J=9 Hz, 2H), 5.07 (d, J=15 Hz, 1H), 4.63 (s, 1H), 4.12 (d, J=15 Hz, 1H), 3.77 (s, 3H), 2.96 (m, 2H), 1.94 (s, 3H), 1.84 (s, 3H). MS: m/z (MNa+) 445.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08680122B2 |
| Source dataset | uspto-grants-2014_03 |
| ORD ID | ord-e873621aaf5244fcad392202f06798e6 |
| Source note | uspto-grants-2014_03 |