HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-[(4-Chlorophenyl)methyl]-4-(3-chloropropyl)piperazine → 3-n-Butyl-4-methyl-7-{3-[4-(4-chlorobenzyl)-piperazin-1-yl]-propoxy}-2-oxo-1,2-dihydroquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-[(4-Chlorophenyl)methyl]-4-(3-chloropropyl)piperazine | HCID 13399727 | — |
| Reactant | 3-n-Butyl-4-methyl-7-hydroxy-2-oxo-1,2-dihydroquinoline | HCID 23330451 | — |
| Solvent | 1-Ethoxyethanol | HCID 10129898 | — |
| Product | 3-n-Butyl-4-methyl-7-{3-[4-(4-chlorobenzyl)-piperazin-1-yl]-propoxy}-2-oxo-1,2-dihydroquinoline | HCID 23330460 | 57.5% |
Reaction Steps
In a manner analogous to that described in Example 1, 3-n-butyl-4-methyl-7-hydroxy-2-oxo-1,2-dihydroquinoline is reacted with 3-[4-(4-chlorobenzyl)-piperazin-1-yl]-propyl chloride in ethoxyethanol. There is obtained 3-n-butyl-4-methyl-7-{3-[4-(4-chlorobenzyl)-piperazin-1-yl]-propoxy}-2-oxo-1,2-dihydroquinoline in a yield of 57.5% of theory; m.p. 148°-149° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04234585 |
| Source dataset | uspto-grants-1980_11 |
| ORD ID | ord-447cb22eb062442487e8dd25611e9edb |
| Source note | uspto-grants-1980_11 |