HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyruvic Acid → N-(1-Carboxyethyl)-L-alanyl-L-proline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyruvic Acid | HCID 1060 | — |
| Reactant | L-Alanyl-L-proline | HCID 83525 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-(1-Carboxyethyl)-L-alanyl-L-proline | HCID 53882949 | 91.5% |
Reaction Steps
A solution of L-alanyl-L-proline (372 mg) and pyruvic acid (881 mg) in water is adjusted to pH 7 and treated with 377 mg of sodium cyanoborohydride at room temperature until reaction is complete. The product is absorbed on strong acid ion-exchange resin and then eluted with 2% pyridine in water. Freeze drying gives 472 mg of N-(1-carboxyethyl)-L-alanyl-L-proline. Nmr and mass spectrogram are consistent with structure. The nmr spectrum shows multiplets centered at 4.5, 3.7, and 2.2 ppm, and a pair of doublets and 1.6 ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04374829 |
| Source dataset | uspto-grants-1983_02 |
| ORD ID | ord-0d684a7e5e644cf7b1121f494b09db25 |
| Source note | uspto-grants-1983_02 |