HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Benzylpiperidin-4-ol → [5-(1-Benzyl-piperidin-4-yloxy)-1H-indol-2-yl]-morpholin-4-yl-methanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Benzylpiperidin-4-ol | HCID 78461 | — |
| Reactant | (5-hydroxy-1H-indol-2-yl)-morpholin-4-yl-methanone | HCID 44185244 | — |
| Product | [5-(1-Benzyl-piperidin-4-yloxy)-1H-indol-2-yl]-morpholin-4-yl-methanone | HCID 69282674 | — |
Reaction Steps
According to the procedure described for the synthesis of Example 1/Step 2 the tide compound was synthesized from (5-hydroxy-1H-indol-2-yl)-morpholin-4-yl-methanone (Example 1, Step 1) and 1-benzyl-4-hydroxy-piperidine (commercially available). (m/e): 419.52 (MH+, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07361682B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-44c5e40388474c579ba2412ff3c72588 |
| Source note | uspto-grants-2008_04 |