HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium formate → Ammonium Hydroxide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | 3-(N-benzyloxycarbonylpyrrolidin-2-ylmethyl)-1H-indole | HCID 12050053 | — |
| Reactant | 3-(N-benzyloxycarbonylpiperid-2-ylmethyl)-1H-indole | HCID 19970244 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ammonium Hydroxide | HCID 14923 | — |
| Product | Indole, 3-(2-piperidylmethyl)- | HCID 21346 | — |
| Product | 3-(pyrrolidin-2-ylmethyl)-1H-indole | HCID 18508996 | — |
Reaction Steps
A mixture of the 3-(N-benzyloxycarbonylpyrrolidin-2-ylmethyl)-1H-indole or the 3-(N-benzyloxycarbonylpiperid-2-ylmethyl)-1H-indole (2.00 mmol), 10% palladium on carbon (0.20 g), and ammonium formate (1.26 g, 20 mmol, 10 eq) in absolute ethanol (15 mL) was stirred under a nitrogen atmosphere for 4 hours. The resulting reaction mixture was filtered through diatomaceous earth, and the filtrate was evaporated under reduced pressure. The residue was column chromatographed using silica gel (approximately 50 g) and elution with a solution of methylene chloride: methanol: ammonium hydroxide [8:2:0.2] or other appropriate solvent system to afford the corresponding 3-(pyrrolidin-2-ylmethyl)-1H-indole or 3-(piperid-2-ylmethyl)-1H-indole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05607951 |
| Source dataset | uspto-grants-1997_03 |
| ORD ID | ord-543a21d4a63d49cba553f08fcbb199e1 |
| Source note | uspto-grants-1997_03 |