HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Methoxyindole → 5-Methoxy-3-(piperidin-4-yl)-1H-indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Methoxyindole | HCID 13872 | — |
| Reactant | 4-Piperidone | HCID 33721 | — |
| Catalyst | Adams' catalyst | HCID 345198 | — |
| Product | 5-Methoxy-3-(piperidin-4-yl)-1H-indole | HCID 43224 | 74% |
Reaction Steps
This compound was prepared following the procedure described in example 1 (parts A and B) starting with 5.9 g (40 mmol) of 5-methoxyindol and 15.5 g (100 mmol) of 4-piperidone. In this case the hydrogenation took place for 24 hours at 30 psi and the catalyst used was platinum (IV) oxide. 6.8 g (74% of yield) of 5-methoxy-3-piperidin-4-yl-1H-indole were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07189741B2 |
| Source dataset | uspto-grants-2007_03 |
| ORD ID | ord-ec2ee785a40c45e881fc369aa5a5b091 |
| Source note | uspto-grants-2007_03 |