HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → HCID 22808903, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzyloxycarbonyl-L-phenylalanine | HCID 70878 | — |
| Reactant | Methanesulfonic acid, 1H-benzotriazol-1-yl ester | HCID 11745953 | — |
| Product | HCID 22808903 | HCID 22808903 | — |
Reaction Steps
N-Benzyloxycarbonyl-L-phenylalanine (1.5 g) and triethylamine (0.7 ml) are dissolved in anhydrous tetrahydrofuran (20 ml). To the solution is added 1-methanesulfonyloxy-1,2,3-benzotriazole (1.10 g) at room temperature and the mixture is stirred for 1 hour, and thereto is further added 28% aqueous ammonia (3.0 ml) and the mixture is stirred for 2 hours. After allowing to stand, the solvent is distilled off under a reduced pressure, and to the residue is added water and the crystals are crushed. The crystals are separated by filtration, washed with water and dried to give N-benzyloxycarbonyl-L-phenylalaninamide (1.15 g), melting point: 158°-160° C. The product is identified with an authentic sample by infrared spectrum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04242507 |
| Source dataset | uspto-grants-1980_12 |
| ORD ID | ord-202863d143fe42b89ab45e5a76acbcc4 |
| Source note | uspto-grants-1980_12 |