HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzylamine → N-benzylpiperidin-4-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Product | N-benzylpiperidin-4-amine | HCID 3016528 | — |
Reaction Steps
The compounds of formula A and G are prepared as is described in Reaction Sequences 1 and 2. Compound G is then treated with sodium cyanoborohydride, optionally in the presence of benzylamine, to produce the 4-(benzyl)amino piperidine which is subsequently coupled with the compound of formula A to produce the benzyl derivative (formula G"). The compound of formula G" is then hydrogenated using, for instance, palladium-on-carbon catalyst to produce the compound of formula I.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04499100 |
| Source dataset | uspto-grants-1985_02 |
| ORD ID | ord-746d12cd9afa47d7b19365652c6d5842 |
| Source note | uspto-grants-1985_02 |