4-Methoxybenzaldehyde → HCID 178488859, compound
Reaction equation
[N+:1]([C:4]1[CH:5]=[C:6]([CH:21]=[CH:22][C:23]=1[N+:24]([O-])=O)[NH:7][C:8](=[O:20])[C:9]1[CH:14]=[CH:13][C:12]([N:15]2[CH:19]=[CH:18][N:17]=[CH:16]2)=[CH:11][CH:10]=1)([O-])=O.[CH3:27][O:28][C:29]1[CH:36]=[CH:35][C:32]([CH:33]=O)=[CH:31][CH:30]=1>>[N:15]1([C:12]2[CH:13]=[CH:14][C:9]([C:8]([NH:7][C:6]3[CH:21]=[CH:22][C:23]4[NH:24][C:33]([C:32]5[CH:35]=[CH:36][C:29]([O:28][CH3:27])=[CH:30][CH:31]=5)=[N:1][C:4]=4[CH:5]=3)=[O:20])=[CH:10][CH:11]=2)[CH:19]=[CH:18][N:17]=[CH:16]1Participants
3
Procedure
Compound 209 was prepared according to the procedure similar to that described in Scheme III from 3,4-dinitro-N-(4-imidazol-1-ylbenzoyl)aniline and 4-methoxybenzaldehyde. [M+H]+ calcd for C24H19N5O2: 410.05; found: 410.00.
Sources & evidence
- ORD record
- ord-0f0c1e4e23994cfd837968bbf1a30c9b
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09144557B2
Reaction notes
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