3,4-dinitro-N-(4-morpholinobenzoyl)aniline → HCID 178521806, compound
Reaction equation
[N+:1]([C:4]1[CH:5]=[C:6]([CH:22]=[CH:23][C:24]=1[N+:25]([O-])=O)[NH:7][C:8](=[O:21])[C:9]1[CH:14]=[CH:13][C:12]([N:15]2[CH2:20][CH2:19][O:18][CH2:17][CH2:16]2)=[CH:11][CH:10]=1)([O-])=O.[CH:28]1([C:31]([N:33]2[CH2:38][CH2:37][N:36]([C:39]3[CH:46]=[CH:45][C:42]([CH:43]=O)=[CH:41][CH:40]=3)[CH2:35][CH2:34]2)=[O:32])[CH2:30][CH2:29]1>>[CH:28]1([C:31]([N:33]2[CH2:34][CH2:35][N:36]([C:39]3[CH:40]=[CH:41][C:42]([C:43]4[NH:25][C:24]5[CH:23]=[CH:22][C:6]([NH:7][C:8](=[O:21])[C:9]6[CH:14]=[CH:13][C:12]([N:15]7[CH2:20][CH2:19][O:18][CH2:17][CH2:16]7)=[CH:11][CH:10]=6)=[CH:5][C:4]=5[N:1]=4)=[CH:45][CH:46]=3)[CH2:37][CH2:38]2)=[O:32])[CH2:29][CH2:30]1Participants
3
Procedure
Compound 415 was prepared according to the procedure similar to that described in Scheme III from 3,4-dinitro-N-(4-morpholinobenzoyl)aniline and 4-(4-cyclopropanecarbonylpiperazinyl)benzaldehyde. [M+H]+ calcd for C32H34N6O3: 551.27; found: 551.10.
Sources & evidence
- ORD record
- ord-3dccdc992c5f4627a39a0ac6bfb7ee6f
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09144557B2
Reaction notes
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