HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium formate → trans-3-(5-fluoro-1H-indol-3-yl)-cyclopentylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | trans-benzyl-3-(5-fluoro-1H-indol-3-yl)-cyclopentylamine | HCID 68830416 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | trans-3-(5-fluoro-1H-indol-3-yl)-cyclopentylamine | HCID 68827696 | 100% |
Reaction Steps
A mixture of trans-benzyl-3-(5-fluoro-1H-indol-3-yl)-cyclopentylamine (0.45 g, 1.46 mmol), 0.20 g 10% Pd/C, and ammonium formate (1.0 g, 15.9 mmol) in methanol (30 mL) were refluxed under nitrogen for 4 hours. The reaction mixture was cooled, filtered through celite, and concentrated. The residue was diluted with 1 N aqueous NaOH (50 mL) and extracted with ethyl acetate (3×50 mL). The combined organic layers were washed with water (50 mL) and brine (50 mL), then were dried over anhydrous sodium sulfate, filtered, and concentrated to give 0.28 g (100%) of the title compound as a thick oil: MS (ESI) m/z 219 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06911445B2 |
| Source dataset | uspto-grants-2005_06 |
| ORD ID | ord-acfa7053bfbf469abdfc8e3ad3dabba3 |
| Source note | uspto-grants-2005_06 |