HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia hydroxide → HCID 59278496, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia hydroxide | HCID 21862953 | — |
| Reactant | HCID 59278335 | HCID 59278335 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 59278496 | HCID 59278496 | — |
Reaction Steps
A solution of N-(5-cyano-pyrimidin-2-yl)-N-methyl-acetamide (0.08 g, 0.45 mmol) in MeOH and 28% aqueous ammonia hydroxide (0.80 mL, 0.45 mmol) was hydrogenated over Raney-Ni catalyst using a continuous flow hydrogenation apparatus (conditions: flow rate 1 mL/minute, 25° C., 10 bar). After 2 hours, the solvent was concentrated in vacuo. The residue was purified by silica gel chromatography eluting with 5% MeOH in CH2Cl2. The major fractions were combined and the solvent was concentrated in vacuo to afford the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07879873B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-36ca984828e34936a4febc747b1ac8a8 |
| Source note | uspto-grants-2011_02 |