HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Methylbenzylamine → N-benzyl-N-methylpiperidine-4-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Methylbenzylamine | HCID 7669 | — |
| Reactant | Benzyl 4-(chlorocarbonyl)piperidine-1-carboxylate | HCID 2776270 | — |
| Product | N-benzyl-N-methylpiperidine-4-carboxamide | HCID 5103038 | — |
Reaction Steps
This compound was prepared similarly to Preparation C starting from 1-benzyloxycarbonylpiperidine-4-carboxylic acid chloride and N-methylbenzylamine, and was used directly in Example 10. This intermediate was characterised as the hydrochloride salt, m.p. 175°-176°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04243666 |
| Source dataset | uspto-grants-1981_01 |
| ORD ID | ord-0399a0cb0319432c8d68d929a598f5c5 |
| Source note | uspto-grants-1981_01 |