HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzylamine → 1-(3-(4-Fluorophenoxy)propyl)-3-methoxypiperidin-4-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | Thiophene | HCID 8030 | — |
| Reactant | 1-[3-(4-Fluorophenoxy)propyl]-3-methoxy-4-piperidinone | HCID 11065870 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(3-(4-Fluorophenoxy)propyl)-3-methoxypiperidin-4-amine | HCID 13677832 | — |
Reaction Steps
A mixture of 1-[3-(4-fluorophenoxy)-propyl]-3-methoxy-4-piperidinone (140 mg, intermediate 1), benzylamine (61 mg), Pd 10% on charcoal (100 mg) and a 0.02% solution of thiophene in THF was reacted under hydrogen gas for 3 hours at 50° C. The catalyst was filtered off and fresh palladium 10% on charcoal (100 mg) was added. Debenzylation of the formed intermediate took place under hydrogen atmosphere for 18 hours at 50° C. The reaction mixture was filtered and evaporated under a gentle stream of nitrogen to yield 1-[3-(4-fluorophenoxy)-propyl]-3-methoxy-4-piperidinamine (compound I-1) having a cis/trans ratio of about 93/7.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06218542B1 |
| Source dataset | uspto-grants-2001_04 |
| ORD ID | ord-1d489020ff774a0087a81308229d10d8 |
| Source note | uspto-grants-2001_04 |