HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-Aminonicotinamide → HCID 86762306, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-Aminonicotinamide | HCID 9500 | — |
| Reactant | HCID 16058694 | HCID 16058694 | — |
| Product | HCID 86762306 | HCID 86762306 | — |
Reaction Steps
The product from Example 1, Part C (160 mg, 0.5 mmol) and 6-aminonicotinamide (103 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, and 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 (10 mg, 5%). 1H NMR (300 MHz, CDCl3) δ 8.76 (d, J=2 Hz, 1H), 8.71 (br s, 1H), 8.22 (d, J=9 Hz, 1H), 8.13 (dd, J=9 Hz, 2 Hz, 1H), 7.20 (d, J=9 Hz, 2H), 6.83 (d, J=9 Hz, 2H), 5.05 (d, J=15 Hz, 1H), 4.63 (s, 1H), 4.13 (d, J=15 Hz, 1H), 3.77 (s, 3H), 2.94 (s, 2H), 1.95 (s, 3H), 1.83 (s, 3H). MS: m/z (MH+) 441.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08680122B2 |
| Source dataset | uspto-grants-2014_03 |
| ORD ID | ord-2ae3e4cf75804f0aa7f939363ffc2bae |
| Source note | uspto-grants-2014_03 |