HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(2-nitro-5-(pyrazin-2-yl)phenyl)pyrrolidine-1-carboxamide → N-(2-amino-5-(pyrazin-2-yl)phenyl)pyrrolidine-1-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(2-nitro-5-(pyrazin-2-yl)phenyl)pyrrolidine-1-carboxamide | HCID 70982085 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(2-amino-5-(pyrazin-2-yl)phenyl)pyrrolidine-1-carboxamide | HCID 71466382 | 70.6% |
Reaction Steps
To a solution of 1 N-(2-nitro-5-(pyrazin-2-yl)phenyl)pyrrolidine-1-carboxamide (0.11 g, 0.35 mmol) in methanol (6 mL) and THF (6 mL) was added Pd/C (0.04 g, 0.94 mmol, 0.33 equiv.). The reaction mixture was degassed then stirred at room temperature under H2 atmosphere for 1h. The reaction was filtered through celite and concentrated. The crude solid was washed with ether, and dried under reduced pressure to obtain of pure N-(2-amino-5-(pyrazin-2-yl)phenyl)pyrrolidine-1-carboxamide (0.07 g, 70% yield). ESI+ MS: m/z 284 ([M+H]+), 1H NMR (500 MHz, d6-DMSO): δ 9.30 (s, 1H), 8.55 (s, 1H), 8.40-8.39 (m, 1H), 7.88 (s, 1H), 7.71-7.69 (m, 1H), 7.53 (s, 1H), 6.81 (d, J=8.5 Hz, 1H), 5.31 (s, 2H), 3.40-3.37 (m, 4H), 1.86 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09365498B2 |
| Source dataset | uspto-grants-2016_06 |
| ORD ID | ord-aab09d77b063443ebc3d0f51a4d8914f |
| Source note | uspto-grants-2016_06 |