HuagongsheHuagongshe Chemistry Print Report · For research reference only
L-Alanyl-L-proline → HCID 54060932, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | L-Alanyl-L-proline | HCID 83525 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 18370942 | HCID 18370942 | — |
| Product | HCID 54060932 | HCID 54060932 | — |
Reaction Steps
In the manner described in Example 26, ethyl-2-oxo-4-(4-fluoro-phenyl)butyrate and L-alanyl-L-proline are condensed in the presence of sodium cyanoborohydride to yield N-[1-ethoxycarbonyl-3-(4-fluorophenyl)-propyl]-L-alanyl-L-proline. The mass spectrum shows a molecular ion at 394, and strong peaks at 376 (M-18, H2O) and 375 (M-19, F). The nmr spectrum is consistent with the proposed structure. Elemental analysis indicates a sesquihydrate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04374829 |
| Source dataset | uspto-grants-1983_02 |
| ORD ID | ord-374ecc5c6d244b0ea8260efb19300268 |
| Source note | uspto-grants-1983_02 |