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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 224775Generated: October 29, 2026

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

https://huagongshe.com/reaction/224775

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-[(4-Chlorophenyl)methyl]-4-(3-chloropropyl)piperazineHCID 13399727—
Reactant3-n-Butyl-4-methyl-7-hydroxy-2-oxo-1,2-dihydroquinolineHCID 23330451—
Solvent1-EthoxyethanolHCID 10129898—
Product3-n-Butyl-4-methyl-7-{3-[4-(4-chlorobenzyl)-piperazin-1-yl]-propoxy}-2-oxo-1,2-dihydroquinolineHCID 2333046057.5%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04234585
Source datasetuspto-grants-1980_11
ORD IDord-447cb22eb062442487e8dd25611e9edb
Source noteuspto-grants-1980_11