HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(4-Methyl-1-piperazine)propan-1-ol → 4-Chloro-6-cyano-7-(3-(4-methylpiperazin-1-yl)propoxy)quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(4-Methyl-1-piperazine)propan-1-ol | HCID 79208 | — |
| Reactant | 4-Chloro-6-cyano-7-(3-(pyrrolidin-1-yl)propoxy)quinoline | HCID 59712234 | — |
| Reactant | 4-Chloro-6-cyano-7-hydroxyquinoline | HCID 135583730 | — |
| Product | 4-Chloro-6-cyano-7-(3-(4-methylpiperazin-1-yl)propoxy)quinoline | HCID 59712233 | 90% |
Reaction Steps
Using an analogous procedure to that described for the preparation of 4-chloro-6-cyano-7-(3-(pyrrolidin-1-yl)propoxy)quinoline, (starting material in Example 11), 4-chloro-6-cyano-7-hydroxyquinoline (8.2 g, 40 mmol), (prepared as described for the starting material in Example 1), was reacted with 1-(3-hydroxypropyl)-4-methylpiperazine (7.6 g, 48 mmol) to give 4-chloro-6-cyano-7-(3-(4-methylpiperazin-1-yl)propoxy)quinoline (12.4 g, 90%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07371765B2 |
| Source dataset | uspto-grants-2008_05 |
| ORD ID | ord-a3e3f372decf40c38f9add0eeb3755a3 |
| Source note | uspto-grants-2008_05 |