HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Bromo-3-pyridinecarboxaldehyde → 1-(5-Bromo-pyridin-3-ylmethyl)-piperidine-4-carboxylic acid cyclohexylamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Bromo-3-pyridinecarboxaldehyde | HCID 2784734 | — |
| Reactant | N-cyclohexylpiperidine-4-carboxamide hydrochloride | HCID 44630870 | — |
| Product | 1-(5-Bromo-pyridin-3-ylmethyl)-piperidine-4-carboxylic acid cyclohexylamide | HCID 86706553 | — |
Reaction Steps
The title compound is prepared according to the reaction 3.01c described above using 5-bromo-pyridine-3-carboxaldehyde and piperidine-4-carboxylic acid cyclohexylamide hydrochloride as in 3.01c: LC-MS A: tR=0.58 min; [M+H]+=380.19.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09428456B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-83b8cc9d597e4c6bb80274f9d35de46d |
| Source note | uspto-grants-2016_08 |