2-(4-bromobutyl)-1H-benzo[de]isoquinoline-1,3(2H)-dione → 2-[5-(4-phenyl-1-piperazinyl)pentyl]-1H-benz[de]isoquinoline-1,3(2H)-dione, hydrochloride
Reaction equation
[ClH:1].[C:2]1([N:8]2[CH2:13][CH2:12][N:11](CCCCN3C(=O)C4C=CC=C5C=4C(=CC=C5)C3=O)[CH2:10][CH2:9]2)[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Br[CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][N:39]1[C:48](=[O:49])[C:47]2[CH:50]=[CH:51][CH:52]=[C:45]3[C:46]=2[C:41](=[CH:42][CH:43]=[CH:44]3)[C:40]1=[O:53].BrCCCCN1C(=O)C2C=CC=C3C=2C(=CC=C3)C1=O>>[ClH:1].[C:2]1([N:8]2[CH2:13][CH2:12][N:11]([CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][N:39]3[C:48](=[O:49])[C:47]4[CH:50]=[CH:51][CH:52]=[C:45]5[C:46]=4[C:41](=[CH:42][CH:43]=[CH:44]5)[C:40]3=[O:53])[CH2:10][CH2:9]2)[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1Participants
4
Reactant 3
Product 1
Procedure
Following the procedure of part (b) of example 34 but substituting 2-(5-bromopentyl)-1H-benz[de]isoquinoline-1,3(2H)-dione for the 2-(4-bromobutyl)-1H-benz[de]isoquinoline-1,3(2H)-dione, one obtains 2-[5-(4-phenyl-1-piperazinyl)pentyl]-1H-benz[de]isoquinoline-1,3(2H)-dione, hydrochloride.
Sources & evidence
- ORD record
- ord-ba19afac4cca48938d71be40e1d48ce9
- Source dataset
- uspto-grants-1976_02
- Patent number
- US03940397
Reaction notes
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