HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Phenylnicotinic acid → 2-Phenylpiperidin-3-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Phenylnicotinic acid | HCID 97489 | — |
| Reactant | 3-Amino-2-phenylpyridine | HCID 2762784 | — |
| Product | 2-Phenylpiperidin-3-amine | HCID 9794008 | — |
Reaction Steps
First, a carboxyl group of a 2-phenylnicotinic acid derivative is amidated and applied to Hofmann's reaction. Then, the resulting 2-phenyl-3-aminopyridine derivative is reduced to produce a 2-phenyl-3-aminopiperidine derivative, and further subjecting the resulting compound to acylation or alkylation, if desired.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07067535B2 |
| Source dataset | uspto-grants-2006_06 |
| ORD ID | ord-d470a022d26b4b1aba454715856cc860 |
| Source note | uspto-grants-2006_06 |