4-formyl-N-phenylbenzamide → HCID 178521917, compound
Reaction equation
[N+:1]([C:4]1[CH:5]=[C:6]([NH:13][C:14]([C:16]2[CH:17]=[N:18][C:19]([N:22]3[CH2:26][CH2:25][CH2:24][CH2:23]3)=[N:20][CH:21]=2)=[O:15])[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>>[C:27]1([NH:33][C:34]([C:36]2[CH:37]=[CH:38][C:39]([C:40]3[NH:10][C:9]4[CH:8]=[CH:7][C:6]([NH:13][C:14]([C:16]5[CH:17]=[N:18][C:19]([N:22]6[CH2:26][CH2:25][CH2:24][CH2:23]6)=[N:20][CH:21]=5)=[O:15])=[CH:5][C:4]=4[N:1]=3)=[CH:42][CH:43]=2)=[O:35])[CH:28]=[CH:29][CH:30]=[CH:31][CH:32]=1Participants
3
Procedure
Compound 221 was prepared according to the procedure similar to that described in Scheme III from N-(3,4-dinitrophenyl)-2-(pyrrolidin-1-yl)pyrimidine-5-carboxamide and 4-phenylaminocarbonylbenzaldehyde. [M+H]+ calcd for C29H25N7O2: 504.22; found: 503.92.
Sources & evidence
- ORD record
- ord-feadfeb31b4e49d69fffb83ffe2c3090
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09144557B2
Reaction notes
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