HuagongsheHuagongshe Chemistry Print Report · For research reference only
methyl (1S,2R)-2-{benzyl[(1R)-1-phenylethyl]amino}-1-methylcyclopentanecarboxylate → methyl (1S,2R)-2-amino-1-methylcyclopentanecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | methyl (1S,2R)-2-{benzyl[(1R)-1-phenylethyl]amino}-1-methylcyclopentanecarboxylate | HCID 86607912 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Formic acid methanol | HCID 18963719 | — |
| Product | methyl (1S,2R)-2-amino-1-methylcyclopentanecarboxylate | HCID 86607913 | 93.2% |
Reaction Steps
According to the procedure of Example 53, Step 2, using methyl (1S,2R)-2-{benzyl[(1R)-1-phenylethyl]amino}-1-methylcyclopentanecarboxylate (1.025 g, 2.92 mmol), 4.4% HCO2H/MeOH (30 mL) and 10% Pd/C (1.058 g), methyl (1S,2R)-2-amino -1-methylcyclopentanecarboxylate (527 mg, 2.72 mmol, 93%) was obtained as a colorless solid. 1H NMR (400 MHz, DMSO-D6) δ ppm 1.29 (s, 3H) 1.56-1.62 (m, 1H) 1.64-1.76 (m, 3H) 2.07-2.13 (m, 1H) 2.15-2.22 (m, 1H) 3.24-3.31 (m, 1H) 3.64-3.71 (m, 3H) 8.18 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07595327B2 |
| Source dataset | uspto-grants-2009_09 |
| ORD ID | ord-fbc15acac26747b2a9494d0fb8823780 |
| Source note | uspto-grants-2009_09 |