HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(1-acetyl-5-nitro-1H-indazol-3-yl)acetamide → N-(1-acetyl-5-amino-1H-indazol-3-yl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(1-acetyl-5-nitro-1H-indazol-3-yl)acetamide | HCID 57755833 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-(1-acetyl-5-amino-1H-indazol-3-yl)acetamide | HCID 57755866 | 98% |
Reaction Steps
The product from Step (b) above (3.0 g, 11.4 mmol) and 5% Pd/C (1 g) were combined in MeOH (40 mL) and hydrogenated uner a balloon of H2 for 3 h. The mixture was filtered through Celite and the filtrate was concentrated to give the title compound as a dark solid (2.6 g, 98%). NMR 1H NMR (400 MHz, DMSO-D6) δ 10.62 (s, 1H), 7.97 (dd, J=7.9, 1.8, 1H), 6.93-6.89 (m, 2H), 5.26 (s, 2H), 2.52 (s, 3H), 2.08 (s, 3H) (MS m/z 233.2 [M+H]+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07560467B2 |
| Source dataset | uspto-grants-2009_07 |
| ORD ID | ord-3fa5aba120e84866967b923e5c38957f |
| Source note | uspto-grants-2009_07 |