HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-fluoro-2-methyl-1H-indol-5-ol → 6-Cyano-4-(4-fluoro-2-methylindol-5-yloxy)-7-(3-(4-methylpiperazin-1-yl)propoxy)quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-fluoro-2-methyl-1H-indol-5-ol | HCID 10352036 | — |
| Reactant | 4-Chloro-6-cyano-7-(3-(4-methylpiperazin-1-yl)propoxy)quinoline | HCID 59712233 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-Cyano-4-(4-fluoro-2-methylindol-5-yloxy)-7-(3-(4-methylpiperazin-1-yl)propoxy)quinoline | HCID 10183887 | 44.3% |
Reaction Steps
Using an analogous procedure to that described in Example 11, 4-chloro-6-cyano-7-(3-(4-methylpiperazin-1-yl)propoxy)quinoline (500 mg, 1.45 mmol) was reacted with 4-fluoro-5-hydroxy-2-methylindole (287 mg, 1.74 mmol), (prepared as described for the starting material in Example 11), in DMF (1 ml) to give 6-cyano-4-(4-fluoro-2-methylindol-5-yloxy)-7-(3-(4-methylpiperazin-1-yl)propoxy)quinoline (304 mg, 44%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07371765B2 |
| Source dataset | uspto-grants-2008_05 |
| ORD ID | ord-74f78843d08746f8893e3f3fa4fd0cfe |
| Source note | uspto-grants-2008_05 |