N-(4-oxo-butyl)-benzamide → (4-Naphthoyl-piperazin-1-yl)-acetaldehyde
Reaction equation
[C:1]1([C:11]([N:13]2[CH2:18][CH2:17][N:16]([CH2:19][CH2:20][OH:21])[CH2:15][CH2:14]2)=[O:12])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1.O=CCCCNC(=O)C1C=CC=CC=1>>[C:1]1([C:11]([N:13]2[CH2:18][CH2:17][N:16]([CH2:19][CH:20]=[O:21])[CH2:15][CH2:14]2)=[O:12])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1Participants
3
Procedure
(4-Naphthoyl-piperazin-1-yl)-acetaldehyde (39C) is prepared from 39B as described for 1E.
Sources & evidence
- ORD record
- ord-9a79c6af3ed547048bfaabbd2c1cae42
- Source dataset
- uspto-grants-2013_03
- Patent number
- US08389555B2
Reaction notes
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