HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 20134255, compound → HCID 20134248, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 20134255 | HCID 20134255 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 20134248 | HCID 20134248 | — |
Reaction Steps
N-(2-[4-Carbomethoxyphenyl]-1-methylethyl)-2-(4-benzyloxy-3-methylsulphonylmethylphenyl)-2-hydroxyethanamine(2.3 g) was converted to the hydrochloride salt and hydrogenated in ethanol (200 ml) in a Parr hydrogenerator at 50 psi and 25° for 2 hours in the presence of 10% palladium on charcoal (0.5 g). The catalyst was removed and the product was isolated as a mixture of diastereoisomers, mp 145°-148° (methanol:ether). τ(d6DMSO) 8.90 (3H, d, J=6 Hz), 7.2 (3H, s), 6.20-7.10 (6H, m), 6.20 (3H, s), 5.70 (2H, s), 5.00 (1H, m), 390 (1H, b), 2.40-3.10 (5H, m), 2.08 (2H, d, J=8 Hz)., 0.70 (1H, br),-0.10 (1H, br).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04478849 |
| Source dataset | uspto-grants-1984_10 |
| ORD ID | ord-972754568be04ce1930cd83c672b3344 |
| Source note | uspto-grants-1984_10 |