HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium borohydride → HCID 53921892, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | Acetic acid methanol | HCID 10129899 | — |
| Reactant | HCID 54258508 | HCID 54258508 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 53921892 | HCID 53921892 | 85.7% |
Reaction Steps
N-[(2-Oxo-1-pyrrolidinyl)acetyl]-L-prolyl-L-proline methyl ester (Compound 1) (2.56 g) as obtained in Example 1 was dissolved in a mixture of THF (30 ml) and ethanol (6 ml), to which was added a THF solution of 2 M lithium borohydride (7.3 ml) under ice-cooling. After 3 hours' stirring at room temperature, a 50% acetic acid-methanol solution was added to adjust the pH of the mixture to 6. The residue obtained by concentration was purified by silica gel column chromatography (chloroform-methanol) to give 2.02 g of N-[(2-oxo-1-pyrrolidinyl)acetyl]-L-prolyl-L-prolinol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05118811 |
| Source dataset | uspto-grants-1992_06 |
| ORD ID | ord-a2e7813f90494cb68597817356162b80 |
| Source note | uspto-grants-1992_06 |