HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-methyl-1H-indol-5-ol → 7-Benzyloxy-6-methoxy-4-(2-methylindol-5-yloxy)quinazoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-methyl-1H-indol-5-ol | HCID 83336 | — |
| Reactant | 7-(Benzyloxy)-4-chloro-6-methoxyquinazoline | HCID 10661998 | — |
| Product | 7-Benzyloxy-6-methoxy-4-(2-methylindol-5-yloxy)quinazoline | HCID 22030804 | 91.2% |
Reaction Steps
Using an analogous procedure to that described in Example 32, 7-benzyloxy-4-chloro-6-methoxyquinazoline (1 g, 3.33 mmol), (prepared as described for the starting material in Example 1), was reacted with 5-hydroxy-2-methylindole (0.59 g, 4 mmol) to give 7-benzyloxy-6-methoxy-4-(2-methylindol-5-yloxy)quinazoline (1.25 g, 91%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08492560B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-fe715dedff4949048f0b2c54172e71c9 |
| Source note | uspto-grants-2013_07 |