4-formyl-N-phenylbenzamide → HCID 178521915, 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][CH2:24][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>>[C:28]1([NH:34][C:35](=[O:36])[C:37]2[CH:38]=[CH:39][C:40]([C:41]3[NH:10][C:9]4[CH:8]=[CH:7][C:6]([NH:13][C:14](=[O:27])[C:15]5[CH:20]=[CH:19][C:18]([N:21]6[CH2:26][CH2:25][CH2:24][CH2:23][CH2:22]6)=[CH:17][CH:16]=5)=[CH:5][C:4]=4[N:1]=3)=[CH:43][CH:44]=2)[CH:29]=[CH:30][CH:31]=[CH:32][CH:33]=1Participants
3
Procedure
Compound 215 was prepared according to the procedure similar to that described in Scheme III from N-(3,4-dinitrophenyl)-4-piperidinylbenzamide and 4-phenylaminocarbonylbenzaldehyde. [M+H]+ calcd for C32H29N5O2: 516.24; found: 516.07.
Sources & evidence
- ORD record
- ord-782f8c1d5758490eb28b5142e48d4f35
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09144557B2
Reaction notes
Loading…