HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-nitro-2-(pyridin-2-yl)-1H-indole → 2-(piperidin-2-yl)-1H-indol-5-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-nitro-2-(pyridin-2-yl)-1H-indole | HCID 59129380 | — |
| Solvent | Hydrochloride methanol | HCID 21893726 | — |
| Product | 2-(piperidin-2-yl)-1H-indol-5-amine | HCID 59129471 | 110.6% |
Reaction Steps
5-Nitro-2-(pyridin-2-yl)-1H-indole (1.0 g, 4.2 mmol) was added to HCl/MeOH (2 M, 50 mL). The reaction mixture was stirred at room temperature for 1 h and the solvent was evaporated under vacuum. PtO2 (200 mg) was added to a solution of the residue in MeOH (50 mL) and the reaction mixture was stirred under hydrogen atmosphere (1 atm) at room temperature for 2 h. The catalyst was filtered through a celite pad and the solvent was evaporated under vacuum to afford 2-(piperidin-2-yl)-1H-indol-5-amine (1.0 g), which was directly used in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08623905B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-0f97acb3d4ff4885bc06424b7ff77a2e |
| Source note | uspto-grants-2014_01 |