4-(4-Morpholinophenyl)aminocarbonylbenzaldehyde → HCID 67686961, compound
Reaction equation
[CH:1]1([C:4]2[O:8][C:7]([CH2:9][O:10][C:11]3[CH:16]=[CH:15][C:14]([N+:17]([O-])=O)=[C:13]([N+:20]([O-])=O)[CH:12]=3)=[N:6][N:5]=2)[CH2:3][CH2:2]1.[O:23]1[CH2:28][CH2:27][N:26]([C:29]2[CH:34]=[CH:33][C:32]([NH:35][C:36]([C:38]3[CH:45]=[CH:44][C:41]([CH:42]=O)=[CH:40][CH:39]=3)=[O:37])=[CH:31][CH:30]=2)[CH2:25][CH2:24]1>>[CH:1]1([C:4]2[O:8][C:7]([CH2:9][O:10][C:11]3[CH:16]=[CH:15][C:14]4[N:17]=[C:42]([C:41]5[CH:40]=[CH:39][C:38]([C:36]([NH:35][C:32]6[CH:31]=[CH:30][C:29]([N:26]7[CH2:25][CH2:24][O:23][CH2:28][CH2:27]7)=[CH:34][CH:33]=6)=[O:37])=[CH:45][CH:44]=5)[NH:20][C:13]=4[CH:12]=3)=[N:6][N:5]=2)[CH2:3][CH2:2]1Participants
3
Procedure
Compound 630 was prepared according to the procedure similar to that described in Scheme III from 1-(5-cyclopropyl-1,3,4-oxadiazol-2-yl)methoxy-3,4-dinitrobenzene and 4-(4-(4-morpholinophenyl)aminocarbonylbenzaldehyde. [M+H]+ calcd for C30H28N6O4: 537.22; found: 537.06.
Sources & evidence
- ORD record
- ord-dc3ba7ca9bdd49d49d6473c02afcf61c
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09144557B2
Reaction notes
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