HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Amlodipine → (2S)-2-aminobutanedioate;3-O-ethyl 5-O-methyl 2-(2-aminoethoxymethyl)-4-(2-chlorophenyl)-6-methyl-1,4-dihydropyridine-3,5-dicarboxylate
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Amlodipine | HCID 2162 | — |
| Edukt | Amlodipine Maleate | HCID 6435922 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | (2S)-2-aminobutanedioate;3-O-ethyl 5-O-methyl 2-(2-aminoethoxymethyl)-4-(2-chlorophenyl)-6-methyl-1,4-dihydropyridine-3,5-dicarboxylate | HCID 86585403 | — |
Reaktionsschritte
16 g of amlodipine and 12 g of amlodipine maleate are melted in a 300 ml flask. The melted substance is cooled to room temperature and dissolved in 300 ml of dichloromethane. The mixture is extracted with 300 ml of a 1M NaOH solution. The organic layer is discarded and the aqueous layer acidified with 55 ml of a 6 M HCl solution. The mixture is extracted with 300 ml of dichloromethane. The layers are separated and the organic layer dried over Na2SO4. The mixture is evaporated to dryness and the resulting waxy solid recrystallized from ethanol. The obtained sticky solid is dried in a vacuum oven at 40° C. leaving 4.7 g of an off white product.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06600047B2 |
| Quelldatensatz | uspto-grants-2003_07 |
| ORD ID | ord-136a5f2dffca4fdf81996f49288e4259 |
| Quellennotiz | uspto-grants-2003_07 |