HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Dioxide → (4-Amino-3-{[3-(cyclohexyl-methyl-amino)-propylamino]-methyl}-phenyl)-phenyl-methanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Thiophene | HCID 8030 | — |
| Reactant | N-Methyl-1,3-propanediamine | HCID 80511 | — |
| Reactant | 5-Benzoyl-2-nitrobenzaldehyde | HCID 19816055 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | (4-Amino-3-{[3-(cyclohexyl-methyl-amino)-propylamino]-methyl}-phenyl)-phenyl-methanone | HCID 58625047 | — |
Reaction Steps
A mixture of 5-benzoyl-2-nitrobenzaldehyde (0.0058 mol) in THF (100 ml) was hydrogenated with 10% Pd/C (1 g) as a catalyst in the presence of 4% thiophene solution (1 mL). After uptake of H2 (3 equiv), the mixture was put in an autoclave. N-cyclohexyl, N-methyl-propane-1,3-diamine (0.01 mol) and CaH2 (0.5 g) were added and the mixture was reacted under 10 atm of CO2 and 50 atm of H2 at 50° C. for 16 hours. When the reaction was complete, the mixture was purified over silica gel on a glass filter (eluent: 90:10 CH2Cl2:(CH3OH:NH3)). The product fractions were collected and the solvent was evaporated to yield the title compound as a residue.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08383637B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-b90822cd5d1d45dea07d384512c8d672 |
| Source note | uspto-grants-2013_02 |