Benzaldehyde, 4-(2-hydroxyethoxy)- → HCID 178482814, compound
Reaction equation
[N+:1]([C:4]1[CH:5]=[C:6]([NH:13][C:14](=[O:24])[C:15]2[CH:20]=[CH:19][C:18]([N:21]([CH3:23])[CH3:22])=[CH:17][CH:16]=2)[CH:7]=[CH:8][C:9]=1[N+:10]([O-])=O)([O-])=O.[OH:25][CH2:26][CH2:27][O:28][C:29]1[CH:36]=[CH:35][C:32]([CH:33]=O)=[CH:31][CH:30]=1>>[CH3:22][N:21]([CH3:23])[C:18]1[CH:19]=[CH:20][C:15]([C:14]([NH:13][C:6]2[CH:7]=[CH:8][C:9]3[NH:10][C:33]([C:32]4[CH:31]=[CH:30][C:29]([O:28][CH2:27][CH2:26][OH:25])=[CH:36][CH:35]=4)=[N:1][C:4]=3[CH:5]=2)=[O:24])=[CH:16][CH:17]=1Participants
3
Procedure
Compound 218 was prepared according to the procedure similar to that described in Scheme III from N-(3,4-dinitrophenyl)-4-dimethylaminobenzamide and 4-(2-hydroxyethyloxy)benzaldehyde. [M+H]+ calcd for C24H24N4O3: 417.19; found: 417.00.
Sources & evidence
- ORD record
- ord-f326cd7ef2d1434eb37243926dbe23b1
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09144557B2
Reaction notes
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