5-(4-Formylbenzylidene)-2,4-thiazolidinedione → HCID 178518439, compound
Reaction equation
[CH:1]([C:3]1[CH:16]=[CH:15][C:6]([CH:7]=[C:8]2[S:12][C:11](=[O:13])[NH:10][C:9]2=[O:14])=[CH:5][CH:4]=1)=O.[Cl:17][C:18]1[C:19]([NH2:26])=[C:20]([NH2:25])[CH:21]=[C:22]([Cl:24])[CH:23]=1>>[Cl:17][C:18]1[C:19]2[NH:26][C:1]([C:3]3[CH:16]=[CH:15][C:6]([CH:7]=[C:8]4[S:12][C:11](=[O:13])[NH:10][C:9]4=[O:14])=[CH:5][CH:4]=3)=[N:25][C:20]=2[CH:21]=[C:22]([Cl:24])[CH:23]=1Participants
3
Procedure
4,6-Dichloro-2-[4-[(2,4-dioxothiazolidin-5-ylidene)methyl]phenyl]benzimidazole was prepared from 5-(4-formylbenzylidene)-2,4-thiazolidinedione and 3,5-dichloro-1,2-phenylenediamine by following General Procedure 2.
Sources & evidence
- ORD record
- ord-a97a4fc70bcd4e2a847afc093ff45026
- Source dataset
- uspto-grants-2002_09
- Patent number
- US06452014B1
Reaction notes
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