HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-Hydroxyquinoline → 5-Allyl-6-methoxyquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-Hydroxyquinoline | HCID 11374 | — |
| Reactant | 1-{1-[2-(6-Methoxy-1-methyl-1,2,3,4-tetrahydroquinolin-7-yl)ethyl]piperidin-4-yl)-1H-indole-6-carboxamide | HCID 57682850 | — |
| Reactant | 1-{1-[2-(1-Acetyl-6-methoxy-1,2,3,4-tetrahydroquinolin-7-yl)ethyl]piperidin-4-yl}-1H-indole-6-carboxamide | HCID 57682875 | — |
| Product | 5-Allyl-6-methoxyquinoline | HCID 57682920 | — |
Reaction Steps
The subject compound was synthesized from 6-hydroxyquinoline according to the methods described in Example 22, (1), (2), and (3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07538123B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-9eece9029cb14a9fad960ce2baeaea82 |
| Source note | uspto-grants-2009_05 |