4-(4-Morpholinophenyl)aminocarbonylbenzaldehyde → HCID 67686750, compound
Reaction equation
[CH2:1]([O:4][C:5]1[CH:10]=[CH:9][C:8]([N+:11]([O-])=O)=[C:7]([N+:14]([O-])=O)[CH:6]=1)[CH:2]=[CH2:3].[O:17]1[CH2:22][CH2:21][N:20]([C:23]2[CH:28]=[CH:27][C:26]([NH:29][C:30]([C:32]3[CH:39]=[CH:38][C:35]([CH:36]=O)=[CH:34][CH:33]=3)=[O:31])=[CH:25][CH:24]=2)[CH2:19][CH2:18]1>>[CH2:1]([O:4][C:5]1[CH:10]=[CH:9][C:8]2[N:11]=[C:36]([C:35]3[CH:34]=[CH:33][C:32]([C:30]([NH:29][C:26]4[CH:25]=[CH:24][C:23]([N:20]5[CH2:19][CH2:18][O:17][CH2:22][CH2:21]5)=[CH:28][CH:27]=4)=[O:31])=[CH:39][CH:38]=3)[NH:14][C:7]=2[CH:6]=1)[CH:2]=[CH2:3]Participants
3
Procedure
Compound 632 was prepared according to the procedure similar to that described in Scheme III from 1-allyloxy-3,4-dinitrobenzene and 4-(4-(4-morpholinophenyl)aminocarbonylbenzaldehyde. [M+H]+ calcd for C27H26N4O3: 455.21; found: 455.00.
Sources & evidence
- ORD record
- ord-134ebef44b114a778dab231d5aa6252a
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09144557B2
Reaction notes
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