HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Methyl-1H-indol-6-ol → HCID 22490038, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Methyl-1H-indol-6-ol | HCID 14878596 | — |
| Reactant | 7-(1-Tert-butoxycarbonylpiperidin-4-ylmethoxy)-4-chloro-6-methoxycinnoline | HCID 22490018 | — |
| Product | HCID 22490038 | HCID 22490038 | — |
Reaction Steps
Using an analogous procedure to that described in Example 8, 7-(1-tert-butoxycarbonylpiperidin-4-ylmethoxy)-4-chloro-6-methoxycinnoline (204 mg, 0.5 mmol) was reacted with 6-hydroxy-2-methylindole (100 mg, 0.55 mmol) to give 7-(1-(tert-butoxycarbonyl)piperidin-4-ylmethoxy)-6-methoxy-4-(2-methylindol-6-yloxy)cinnoline. The crude product was then treated with TFA to give 6-methoxy-4-(2-methylindol-6-yloxy)-7-(piperidin-4-ylmethoxy)cinnoline (10 mg, 4%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06887874B2 |
| Source dataset | uspto-grants-2005_05 |
| ORD ID | ord-1cd292265e54425e9738bd80b7c271c3 |
| Source note | uspto-grants-2005_05 |