HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Benzyl-4-(methylamino)piperidine-4-carboxamide → 4-(Methylamino)piperidine-4-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Benzyl-4-(methylamino)piperidine-4-carboxamide | HCID 96411 | — |
| Reactant | HCID 23541247 | HCID 23541247 | — |
| Product | 4-(Methylamino)piperidine-4-carboxamide | HCID 96474 | — |
Reaction Steps
The 1-isopropyl-4-(methylamino)piperidine-4-carboxamide used as starting material was prepared as follows: 1-benzyl-4-(methylamino)piperidine-4-carboxamide (J Med Chem., 1998, 41(25), 5084) may be deprotected by hydrogenation using an analogous method to that described for the equivalent step in Example 74 to give 4-(methylamino)piperidine-4-carboxamide; 1H NMR Spectrum: 1.35 (m, 2H); 1.68 (m, 2H); 1.93 (brs, 1H); 2.06 (s, 3H), 2.59 (m, 2H); 2.71 (m, 2H); 6.81 (s, 1H); 7.14 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07632840B2 |
| Source dataset | uspto-grants-2009_12 |
| ORD ID | ord-6d666387f56c43278fd1d44162059019 |
| Source note | uspto-grants-2009_12 |