HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Ethanol → N-Boc-4-cyanophenylalanine-N-methylamide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Ethanol | HCID 702 | — |
| Edukt | Methylamine | HCID 6329 | — |
| Edukt | 4-Methylmorpholine | HCID 7972 | — |
| Edukt | Pentafluorophenol | HCID 13041 | — |
| Edukt | N-(tert-Butoxycarbonyl)-4-cyano-L-phenylalanine | HCID 7020841 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | N-Boc-4-cyanophenylalanine-N-methylamide | HCID 22851210 | 92% |
Reaktionsschritte
A solution of N-Boc-4-cyanophenylalanine (1.92 g, 6.6 mmol) and pentafluorophenol (2.43 g, 13.2 mmol) in CH2Cl2 (30 ml) at 0° C. was treated with 4-methylmorpholine (0.74 g, 7.3 mmol). After stirring the reaction mixture for 3 hours, 8M methylamine in ethanol (15 ml, 19.8 mmol) was added and the reaction mixture left to stir at room temperature for 16 hours. The solvent was removed under pressure, the residue dissolved in CH2Cl2 (50 ml) and washed with saturated sodium bicarbonate (2×50 ml), 1M citric acid (2×50 ml) and brine (50 ml). The CH2Cl2 layer was dried over MgSO4 and the solvent removed under pressure to yield the title compound as a white solid (1.84 g, 92%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05412145 |
| Quelldatensatz | uspto-grants-1995_05 |
| ORD ID | ord-a67bf3e8d4a2491c9a876d6e5cb62b11 |
| Quellennotiz | uspto-grants-1995_05 |