HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzylamine → HCID 86641242, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | HCID 86641243 | HCID 86641243 | — |
| Product | HCID 86641242 | HCID 86641242 | — |
Reaction Steps
a method, wherein the amino group of L-aspartic acid is protected, the carboxy group is reduced, the resulting hydroxyl group is converted into a leaving group, the resultant is reacted with ammonia to produce (S)-3-(tert-butoxycarbonyloxyamino) piperidine, the piperidine is reacted with benzylamine instead of ammonia to obtain (S)-1-benzyl-3-(tert-butoxycarbonyloxyamino) piperidine, and deprotection is carried out using trifluoroacetic acid to produce (S)-1-benzyl-3-aminopiperidine (Non-patent Document 3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08338142B2 |
| Source dataset | uspto-grants-2012_12 |
| ORD ID | ord-61bf8672dbbd4ace970e727f0372a7ae |
| Source note | uspto-grants-2012_12 |