HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 4-(N-benzyloxycarbonyl-L-valyloxy)benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 4-Methoxybenzyl 4(N-benzyloxycarbonyl-L-valyloxy)benzoate | HCID 23387546 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(N-benzyloxycarbonyl-L-valyloxy)benzoic acid | HCID 54468851 | — |
Reaction Steps
4-Methoxybenzyl 4-(N-benzyloxycarbonyl-L-valyloxy)benzoate was de-esterified by the method described in Example A-I-1, step c. The title compound (1.86 g) was obtained after silica gel column chromatography (2, 10, 20% ethanol in dichloromethane). Rf (2%MeOH/CHCl3) 0.20. The compound can be activated and esterifed 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-269ce38a4f57460aacf666cb7bee0faa |
| Source note | uspto-grants-2002_10 |