HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(5-nitropyrimidin-2-yl)acetamide → N-(5-aminopyrimidin-2-yl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(5-nitropyrimidin-2-yl)acetamide | HCID 45071770 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-(5-aminopyrimidin-2-yl)acetamide | HCID 20387481 | — |
Reaction Steps
To N-(5-nitropyrimidin-2-yl)acetamide (0.54 g, 3.0 mmol) suspended in EtOH (20 mL) under N2 was added palladium, 10 wt. % on activated carbon (0.32 g, 0.3 mmol). The reaction mixture was hydrogenated under 1 atm of H2 at RT for 2 h and then filtered through a pad of celite and washed with MeOH. The filtrate was concentrated to give N-(5-aminopyrimidin-2-yl)acetamide as a light-yellow solid. MS (ESI, pos. ion) m/z: 153 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07872128B2 |
| Source dataset | uspto-grants-2011_01 |
| ORD ID | ord-fd1f2a3caa724de3b8536cf547ac63e8 |
| Source note | uspto-grants-2011_01 |