HuagongsheHuagongshe Chemistry Print Report · For research reference only
methyl N-{[4-({[(benzyloxy)carbonyl]amino}methyl)cyclohexyl]carbonyl}-L-norleucinate → methyl N-{[4-(aminomethyl)cyclohexyl]carbonyl}-L-norleucinate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | methyl N-{[4-({[(benzyloxy)carbonyl]amino}methyl)cyclohexyl]carbonyl}-L-norleucinate | HCID 69803360 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | methyl N-{[4-(aminomethyl)cyclohexyl]carbonyl}-L-norleucinate | HCID 66920885 | — |
Reaction Steps
A mixture of methyl N-{[4-({[(benzyloxy)carbonyl]amino}methyl)cyclohexyl]carbonyl}-L-norleucinate (830 mg, 1.98 mmol), 10% palladium on C (0.056 g) in methanol (10 mL) was stirred under an atmosphere of hydrogen for 4 hours. The mixture was filtered through diatomaceous earth and the filter cake washed with methanol (2×15 mL). The combined methanol was concentrated under reduced pressure to provide the titled compound as a colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06972340B2 |
| Source dataset | uspto-grants-2005_12 |
| ORD ID | ord-007b4075ba5344d39cd1463e8a2d0912 |
| Source note | uspto-grants-2005_12 |