Sodium Hydroxide → HCID 178481637, compound
Reaction equation
C([N:4]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[C:6](=[C:13](OCC)[C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[C:5]1=[O:23])(=O)C.[NH2:24][C:25]1[CH:35]=[CH:34][C:28]2[N:29]([CH3:33])[C:30](=[O:32])[NH:31][C:27]=2[CH:26]=1.[OH-].[Na+]>CN(C=O)C.CO>[CH3:33][N:29]1[C:28]2[CH:34]=[CH:35][C:25]([NH:24]/[C:13](=[C:6]3\[C:5](=[O:23])[NH:4][C:12]4[C:7]\3=[CH:8][CH:9]=[CH:10][CH:11]=4)/[C:14]3[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=3)=[CH:26][C:27]=2[NH:31][C:30]1=[O:32]Participants
6
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
Prepared from 1-acetyl-3-{1-ethoxy-1-phenylmethylidene}-2-indolinone and 3 equivalents of crude 5-amino-1-methyl-2-oxo-2,3-dihydro-1H-benzimidazole in DMF followed by treatment with 1N sodium hydroxide solution in MeOH.
Sources & evidence
- ORD record
- ord-192519ceeafe40658ff16084c6c9f95a
- Source dataset
- uspto-grants-2000_03
- Patent number
- US06043254
Reaction notes
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