2,6-Dihydroxy-4-methylquinoline → 4-Methyl-6-{3-[4-(4-methylbenzyl)-piperazin-1-yl]-propoxy}-2-oxo-1,2-dihydroquinoline
Reaction equation
[CH3:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([OH:12])[CH:10]=2)[NH:5][C:4](=[O:13])[CH:3]=1.[CH3:14][C:15]1[CH:31]=[CH:30][C:18]([CH2:19][N:20]2[CH2:25][CH2:24][N:23]([CH2:26][CH2:27][CH2:28]Cl)[CH2:22][CH2:21]2)=[CH:17][CH:16]=1>>[CH3:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([O:12][CH2:28][CH2:27][CH2:26][N:23]3[CH2:22][CH2:21][N:20]([CH2:19][C:18]4[CH:17]=[CH:16][C:15]([CH3:14])=[CH:31][CH:30]=4)[CH2:25][CH2:24]3)[CH:10]=2)[NH:5][C:4](=[O:13])[CH:3]=1Participants
3
Procedure
4-Methyl-6-hydroxy-2-oxo-1,2dihydroquinoline is reacted with 3-[4-(4-methylbenzyl)-piperazin-1-yl]-propyl chloride in a manner analogous to that described in Example 5. There is obtained 4-methyl-6-{3-[4-(4-methylbenzyl)-piperazin-1-yl]-propoxy}-2-oxo-1,2-dihydroquinoline which, after recrystallization from diethyl ether, melts at 162°-163° C.
Sources & evidence
- ORD record
- ord-0e93f41cd52c4c9799366a4f830ad429
- Source dataset
- uspto-grants-1980_11
- Patent number
- US04234585
Reaction notes
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