HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 2-(Acetamido)-6-(2-aminoethyl)quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Ninhydrin | HCID 10236 | — |
| Reactant | 2-(Acetamido)-6-(cyanomethyl)quinoline | HCID 118252190 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(Acetamido)-6-(2-aminoethyl)quinoline | HCID 118252183 | — |
Reaction Steps
Compound 47 (0.060 g, 0.266 mmol) was diluted in absolute EtOH (7 mL) and methanolic ammonia (7 N, 7 mL) was added. Raney nickel (˜1.5 g, washed with H2O and MeOH) was added, and the mixture was degassed and hydrogenated with a balloon at room temperature for 30 min while stirring rapidly. The clear solution was decanted away from the nickel and was filtered through a Pall 0.2 μm syringe filter to remove fine particulate matter. The solution was concentrated and dried in vacuo to yield a colorless gum that became a white semisolid upon standing (0.050 g, 82%). Conversion to this amine was confirmed by 1H NMR spectrometry, TLC, MS, and ninhydrin staining, and it was used crude without any further characterization or purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09212144B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-e227a6b8e231457492184a031fe6837e |
| Source note | uspto-grants-2015_12 |