HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → N-[(Benzyloxy)carbonyl]-L-isoleucyl-L-prolyl-L-prolinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | N-[(Benzyloxy)carbonyl]-L-isoleucyl-L-prolyl-L-proline | HCID 54515815 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | N-[(Benzyloxy)carbonyl]-L-isoleucyl-L-prolyl-L-prolinamide | HCID 53756909 | — |
Reaction Steps
Benzyloxycarbonyl-isoleucyl-prolyl-proline (4.5 g) is dissolved in a mixture of tetrahydrofuran (30 ml) and triethylamine (1.4 ml). The solution is chilled in a -5° cooling bath and isobutyl chloroformate (1.6 ml) is added. The solution is allowed to warm to room temperature (10 minutes) and concentrated aqueous ammonia (10 ml) is added. After four hours stirring at room temperature, the reaction is concentrated in vacuo, diluted with ethyl acetate and washed sequentially with saturated sodium bicarbonate, water, 0.1 N hydrochloric acid and water. The organic phase is dried over magnesium sulfate and concentrated to dryness in vacuo to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03973006 |
| Source dataset | uspto-grants-1976_08 |
| ORD ID | ord-ba999c62b81b408e83dcc33283325721 |
| Source note | uspto-grants-1976_08 |