4-formyl-N-phenylbenzamide → HCID 178484444, compound
Reaction equation
[N+:1]([C:4]1[CH:5]=[C:6]([NH:13][C:14](=[O:26])[C:15]2[CH:20]=[CH:19][C:18]([N:21]([CH3:25])[CH2:22][CH2:23][OH:24])=[CH:17][CH:16]=2)[CH:7]=[CH:8][C:9]=1[N+:10]([O-])=O)([O-])=O.[C:27]1([NH:33][C:34]([C:36]2[CH:43]=[CH:42][C:39]([CH:40]=O)=[CH:38][CH:37]=2)=[O:35])[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1>>[OH:24][CH2:23][CH2:22][N:21]([CH3:25])[C:18]1[CH:19]=[CH:20][C:15]([C:14]([NH:13][C:6]2[CH:7]=[CH:8][C:9]3[NH:10][C:40]([C:39]4[CH:38]=[CH:37][C:36]([C:34](=[O:35])[NH:33][C:27]5[CH:28]=[CH:29][CH:30]=[CH:31][CH:32]=5)=[CH:43][CH:42]=4)=[N:1][C:4]=3[CH:5]=2)=[O:26])=[CH:16][CH:17]=1Participants
3
Procedure
Compound 214 was prepared according to the procedure similar to that described in Scheme III from N-(3,4-dinitrophenyl)-4-(N-methyl-N-2-hydroxyethylamino)benzamide and 4-phenylaminocarbonylbenzaldehyde. [M+H]+ calcd for C30H27N5O3: 506.22; found: 506.01.
Sources & evidence
- ORD record
- ord-8f2bcb07dfb24e249d3b1c4715a1d1e3
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09144557B2
Reaction notes
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