HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 15485436, compound → HCID 15485445, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 15485436 | HCID 15485436 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 15485445 | HCID 15485445 | 100.4% |
Reaction Steps
A mixture of of 1-[2-(4-amino-3-nitrophenoxy)ethyl]-2-benzylpiperidine (705 mg, 1.99 mmol) and Raney Ni (about 200 mg) in EtOH (15 mL) was shaken under H2 (35-25 parr) for 4 h, then filtered. The filtrate was evapoated, and the residure was purified by chromatography over silica gel (CHCl3 --MeOH, 3:2) to give 2-benzyl-1-[(3,4-diaminophenoxy)ethyl]piperidine (650 mg, 98%) as a brown viscous oil. 1H NMR (CDCl3): 1.22-1.32 (m, 2H), 1.49-1.52 (m, 3H), 2.49-2.56 (m, 2H), 2.756 (bs, 2H, NH2), 2.96-3.06 (m, 2H), 3.13-3.24 (m, 2H), 3.520 (bs, 2H, NH2), 4.02-4.12 (m, 2H), 6.285 (dd, 1H, J=9; 3), 6.350 (d, 1H, J=3), 6.640 (d, 1H, J=9), 7.16-7.30 (m, 5H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06124317 |
| Source dataset | uspto-grants-2000_09 |
| ORD ID | ord-981fd027996a4006bc301e1a17894d91 |
| Source note | uspto-grants-2000_09 |