HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-methyl-1H-indazol-5-ol → 5-(azepin-4-yloxy)-4-methyl-1H-indazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-methyl-1H-indazol-5-ol | HCID 22933546 | — |
| Reactant | 6-methyl-1H-indazol-5-ol | HCID 22934018 | — |
| Reactant | HCID 178515016 | HCID 178515016 | — |
| Product | 5-(azepin-4-yloxy)-4-methyl-1H-indazole | HCID 22933510 | — |
Reaction Steps
The following compound of Example 408 was synthesized by carrying out reaction according to the method described in Example 385, except for using the cis-2-(4-hydroxycyclohexyl)-1H-isoindole-1,3(2H)-dione obtained in Example 323, (c) and the 4-methyl-1H-indazol-5-ol obtained in Example 402, as starting materials.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07199147B2 |
| Source dataset | uspto-grants-2007_04 |
| ORD ID | ord-9ab61364c48340749421189c808884a2 |
| Source note | uspto-grants-2007_04 |