HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(5-Nitro-pyrimidin-2-yl)-benzamide → N-(5-aminopyrimidin-2-yl)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(5-Nitro-pyrimidin-2-yl)-benzamide | HCID 57699955 | — |
| Catalyst | Platinum | HCID 23939 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-(5-aminopyrimidin-2-yl)benzamide | HCID 11499482 | 14.2% |
Reaction Steps
10% Platinum on carbon (71 mg, 0.036 mmol) was added to a solution 2-(N-benzoyl)amino-5-nitropyrimidine (733 mg, 3.00 mmol) in ethanol (100 ml) at ambient temperature and the reaction stirred for 1 hour under an atmosphere of hydrogen. The reaction was filtered through a pad of celite and the solvents were evaporated in vacuo. Purification by flash chromatography on silica gel, eluting with 5% methanol in dichloromethane yielded 2-(N-benzoyl)amino-5-aminopyrimidine (91 mg, 14% yield) as white solid:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07235559B1 |
| Source dataset | uspto-grants-2007_06 |
| ORD ID | ord-6c3114e433d3424f97430d256d64ca11 |
| Source note | uspto-grants-2007_06 |