HCID 85599795, compound → HCID 67687330, compound
Reaction equation
[CH:1]1([CH2:4][O:5][C:6]2[CH:11]=[CH:10][C:9]([N+:12]([O-])=O)=[C:8]([N+:15]([O-])=O)[CH:7]=2)[CH2:3][CH2:2]1.[O:18]1[CH2:23][CH2:22][N:21]([C:24]2[CH:29]=[CH:28][C:27]([NH:30][C:31]([C:33]3[CH:40]=[CH:39][C:36]([CH:37]=O)=[CH:35][CH:34]=3)=[O:32])=[CH:26][CH:25]=2)[CH2:20][CH2:19]1>>[CH:1]1([CH2:4][O:5][C:6]2[CH:11]=[CH:10][C:9]3[N:12]=[C:37]([C:36]4[CH:35]=[CH:34][C:33]([C:31]([NH:30][C:27]5[CH:26]=[CH:25][C:24]([N:21]6[CH2:20][CH2:19][O:18][CH2:23][CH2:22]6)=[CH:29][CH:28]=5)=[O:32])=[CH:40][CH:39]=4)[NH:15][C:8]=3[CH:7]=2)[CH2:3][CH2:2]1Participants
3
Procedure
Compound 640 was prepared according to the procedure similar to that described in Scheme III from 1-cyclopropylmethoxy-3,4-dinitrobenzene and 4-(4-(4-morpholinophenyl)aminocarbonylbenzaldehyde. [M+H]+ calcd for C28H28N4O3: 469.22; found: 469.03.
Sources & evidence
- ORD record
- ord-94e6fc6e4d2447c4b9af8eadb27d34d5
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09144557B2
Reaction notes
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