4-formyl-N-phenylbenzamide → HCID 178521916, compound
Reaction equation
[N+:1]([C:4]1[CH:5]=[C:6]([NH:13][C:14](=[O:27])[C:15]2[CH:20]=[CH:19][C:18]([N:21]3[CH2:26][CH2:25][O:24][CH2:23][CH2:22]3)=[CH:17][CH:16]=2)[CH:7]=[CH:8][C:9]=1[N+:10]([O-])=O)([O-])=O.[C:28]1([NH:34][C:35]([C:37]2[CH:44]=[CH:43][C:40]([CH:41]=O)=[CH:39][CH:38]=2)=[O:36])[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1>>[O:24]1[CH2:25][CH2:26][N:21]([C:18]2[CH:19]=[CH:20][C:15]([C:14]([NH:13][C:6]3[CH:7]=[CH:8][C:9]4[NH:10][C:41]([C:40]5[CH:39]=[CH:38][C:37]([C:35](=[O:36])[NH:34][C:28]6[CH:29]=[CH:30][CH:31]=[CH:32][CH:33]=6)=[CH:44][CH:43]=5)=[N:1][C:4]=4[CH:5]=3)=[O:27])=[CH:16][CH:17]=2)[CH2:22][CH2:23]1Participants
3
Procedure
Compound 217 was prepared according to the procedure similar to that described in Scheme III from N-(3,4-dinitrophenyl)-4-morpholinylbenzamide and 4-phenylaminocarbonylbenzaldehyde. [M+H]+ calcd for C31H27N5O3: 518.22; found: 518.03.
Sources & evidence
- ORD record
- ord-0a0340e95cbc419bb16a7802c3499282
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09144557B2
Reaction notes
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