HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 15339Erstellt: 23. Oktober 2026
Ammonium Bicarbonate → (cis)-4-Hydroxy-1-(phenylmethyl)-3-piperidinecarboxamide
https://huagongshe.com/de/reaction/15339
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ammonium Bicarbonate | HCID 14013 | — |
| Edukt | HOAt | HCID 181649 | — |
| Edukt | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Edukt | (cis)-4-Hydroxy-1-(phenylmethyl)-3-piperidinecarboxylic acid sodium salt | HCID 131728173 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | (cis)-4-Hydroxy-1-(phenylmethyl)-3-piperidinecarboxamide | HCID 68684194 | 109,6% |
Reaktionsschritte
To a solution of (cis)-4-hydroxy-1-(phenylmethyl)-3-piperidinecarboxylic acid sodium salt (17 g) and 1-hydroxy-7-azabenzotriazole (5 g, 37 mmol) in N,N-dimethylformamide was added N-[3-(dimethylamino)propyl]-N′-ethylcarbodiimide hydrochloride (14.1 g, 73.4 mmol), followed by ammonium bicarbonate (21 g, 26.6 mmol). The reaction mixture was stirred at room temperature for 18 h. The solvent was then removed under reduced pressure and the residue was treated with aqueous sodium bicarbonate solution. The aqueous phase was extracted with 9:1 dichloromethane:methanol mixture. The organic layer was dried (MgSO4) and the solvent was removed under reduced pressure. The residue was subjected to column chromatography on silica gel using a methanol and dichloromethane gradient (0-20% methanol/dichloromethane). This provided the desired compound (9.5 g, 62%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US07732461B2 |
|---|
| Quelldatensatz | uspto-grants-2010_06 |
|---|
| ORD ID | ord-52297c47cb074e87971b38222413d726 |
|---|
| Quellennotiz | uspto-grants-2010_06 |
|---|