HuagongsheHuagongshe Chemistry Print Report · For research reference only
L-Alanyl-L-proline → HCID 12718473, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | L-Alanyl-L-proline | HCID 83525 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 18964897 | HCID 18964897 | — |
| Product | HCID 12718473 | HCID 12718473 | — |
Reaction Steps
In the manner described in example 24, 4-(3-indolyl)-2-oxobutyric acid and L-alanyl-L-proline are condensed in the presence of sodium cyanoborohydride to yield N-[1-carboxy-3-(3-indolyl)propyl]L-alanyl-L-proline. The mass spectrum of the trisilyated material shows a molecular ion at 603 m/e and a M+ -15 peak at 588 m/e.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04472380 |
| Source dataset | uspto-grants-1984_09 |
| ORD ID | ord-1a45d446936a4af5b726ee9a2c3b31e0 |
| Source note | uspto-grants-1984_09 |