HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,6-Dihydroxy-4-methylquinoline → 4-Methyl-6-{3-[4-(2-propoxybenzyl)-piperazin-1-yl]-propoxy}-2-oxo-1,2-dihydroquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,6-Dihydroxy-4-methylquinoline | HCID 600288 | — |
| Reactant | 3-[4-(2-Propoxybenzyl)-piperazin-1-yl]-propyl chloride | HCID 23330455 | — |
| Product | 4-Methyl-6-{3-[4-(2-propoxybenzyl)-piperazin-1-yl]-propoxy}-2-oxo-1,2-dihydroquinoline | HCID 23330446 | 53% |
Reaction Steps
In a manner analogous to that described in Example 9, 4-methyl-6-hydroxy-2-oxo-1,2-dihydroquinoline is reacted with 3-[4-(2-propoxybenzyl)-piperazin-1-yl]-propyl chloride. There is obtained 4-methyl-6-{3-[4-(2-propoxybenzyl)-piperazin-1-yl]-propoxy}-2-oxo-1,2-dihydroquinoline in a yield of 53% of theory in the form of an oily base. The corresponding hydrochloride is obtained from an acetone solution of the base, by the addition of ethereal hydrochloric acid, in amorphous fomrm with a melting point of about 140°-145° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04234585 |
| Source dataset | uspto-grants-1980_11 |
| ORD ID | ord-8679bafa36554799b98c40748006d5d9 |
| Source note | uspto-grants-1980_11 |