HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → N-Boc-4-cyanophenylalanine-N-methylamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Pentafluorophenol | HCID 13041 | — |
| Reactant | N-(tert-Butoxycarbonyl)-4-cyano-L-phenylalanine | HCID 7020841 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-Boc-4-cyanophenylalanine-N-methylamide | HCID 22851210 | 92% |
Reaction Steps
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 methylazine 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%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05300674 |
| Source dataset | uspto-grants-1994_04 |
| ORD ID | ord-9949f6ba5f064ab3845911c82f62e8b6 |
| Source note | uspto-grants-1994_04 |