HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl 3-{5-[3-(benzyloxycarbonylamino)propoxy]-indolyl}propanoate → Methyl 3-[5-(aminopropoxy)indolyl]propanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl 3-{5-[3-(benzyloxycarbonylamino)propoxy]-indolyl}propanoate | HCID 22570338 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Methyl 3-[5-(aminopropoxy)indolyl]propanoate | HCID 66819503 | — |
Reaction Steps
A mixture of methyl 3-{5-[3-(benzyloxycarbonylamino)propoxy]indolyl}propanoate (300 mg, 0.73 mmol), as prepared in the preceding step, 10% palladium(0) on carbon (50 mg) in ethanol (20 mL) was stirred at ambient temperature under hydrogen (balloon) for 3 h. The catalyst was removed by filtration through Celite. The filtrate was concentrated to give the title compound as an off white solid (150 mg, 74%). 1H-NMR (400 MHz, CDCl3/CD3OD) δ 7.25 (d, J=8.9 Hz, 1H), 7.13 (d, J=2.6 Hz, 1H), 7.08 (d, J=2.5 Hz, 1H), 6.85 (dd, J=8.9, 2.5 Hz, 1H), 6.38 (d, J=2.9 Hz, 1H), 4.43 (t, J=6.8 Hz, 2H), 4.10 (t, J=5.8 Hz, 2H), 3.66 (s, 3H), 3.01 (q, J=7.0 Hz, 2H), 2.83 (t, J=6.8 Hz, 2H), 2.04 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07241789B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-d989f579e6164c1aa0a8ed0ca72ac994 |
| Source note | uspto-grants-2007_07 |