HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 54221625, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | HCID 54417723 | HCID 54417723 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 54221625 | HCID 54221625 | — |
Reaction Steps
4-methoxybenzyl 2-(N-benzyloxycarbonyl-L-valyloxy)-3-methyl-(S)-(+)-butyrate was de-esterified by the method described in Example A-I-1, step C. The title compound (3.41 g) was obtained after silica gel column chromatography (2, 10, 20% ethanol in dichloromethane). Rf (2%MeOH/CHCl3) 0.45. The compound may be activated and esterified directly to a drug or further modified as described below:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06458772B1 |
| Source dataset | uspto-grants-2002_10 |
| ORD ID | ord-91ec261ce04e4a80bbb0249c214c74e9 |
| Source note | uspto-grants-2002_10 |