2-Methoxyethoxy-3,4-dinitrobenzene → HCID 67686957, compound
Reaction equation
[CH3:1][O:2][CH2:3][CH2:4][O:5][C:6]1[CH:11]=[CH:10][C:9]([N+:12]([O-])=O)=[C:8]([N+:15]([O-])=O)[CH:7]=1.[O:18]1[CH2:23][CH2:22][N:21]([CH2:24][CH2:25][N:26]2[C:34]3[C:29](=[CH:30][C:31]([NH:35][C:36]([C:38]4[CH:45]=[CH:44][C:41]([CH:42]=O)=[CH:40][CH:39]=4)=[O:37])=[CH:32][CH:33]=3)[CH:28]=[CH:27]2)[CH2:20][CH2:19]1>>[CH3:1][O:2][CH2:3][CH2:4][O:5][C:6]1[CH:11]=[CH:10][C:9]2[N:12]=[C:42]([C:41]3[CH:40]=[CH:39][C:38]([C:36]([NH:35][C:31]4[CH:30]=[C:29]5[C:34](=[CH:33][CH:32]=4)[N:26]([CH2:25][CH2:24][N:21]4[CH2:20][CH2:19][O:18][CH2:23][CH2:22]4)[CH:27]=[CH:28]5)=[O:37])=[CH:45][CH:44]=3)[NH:15][C:8]=2[CH:7]=1Participants
3
Procedure
Compound 676 was prepared according to the procedure similar to that described in Scheme III from 1-(2-methoxyethoxy-3,4-dinitrobenzene and 4-(1-(2-morpholinoethyl)-5-indolylaminocarbonyl)benzaldehyde. [M+H]+ calcd for C31H33N5O4: 540.26; found: 540.10.
Sources & evidence
- ORD record
- ord-86eaf41f6cbb48b4a7f2e0baffd3d4d4
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09144557B2
Reaction notes
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