HuagongsheHuagongshe Chemistry Print Report · For research reference only
L-Alanyl-L-proline → HCID 54172182, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | L-Alanyl-L-proline | HCID 83525 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 20445815 | HCID 20445815 | — |
| Product | HCID 54172182 | HCID 54172182 | — |
Reaction Steps
In the manner described in Example 26, ethyl-2-oxo-4-(2-chlorophenyl)butyrate and L-alanyl-L-proline are condensed in the presence of sodium cyanoborohydride to yield N-[1-ethoxycarbonyl-3-(2-chlorophenyl)-propyl]-L-alanyl-L-proline. The mass spectrum shows a peak at 411, (M+1), and a strong peak at 392, (M-18).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04374829 |
| Source dataset | uspto-grants-1983_02 |
| ORD ID | ord-95f05e6df9f146c2ab2bfb936a080a0a |
| Source note | uspto-grants-1983_02 |