Sodium Hydroxide → HCID 22407400, compound
Reaction equation
[CH2:1]([C:5]1[N:9]([CH2:10][C:11]2[CH:16]=[CH:15][C:14]([N:17]([CH:21]([C:28]([O:30]CC)=[O:29])[C:22]3[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=3)[C:18](=[O:20])[CH3:19])=[CH:13][CH:12]=2)[C:8]2[CH:33]=[CH:34][CH:35]=[CH:36][C:7]=2[N:6]=1)[CH2:2][CH2:3][CH3:4].[OH-].[Na+]>C(O)C>[CH2:1]([C:5]1[N:9]([CH2:10][C:11]2[CH:12]=[CH:13][C:14]([N:17]([CH:21]([C:28]([OH:30])=[O:29])[C:22]3[CH:23]=[CH:24][CH:25]=[CH:26][CH:27]=3)[C:18](=[O:20])[CH3:19])=[CH:15][CH:16]=2)[C:8]2[CH:33]=[CH:34][CH:35]=[CH:36][C:7]=2[N:6]=1)[CH2:2][CH2:3][CH3:4]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Prepared analogously to Example 1b from 2-n-butyl-1-[4-[(α-ethoxycarbonyl)-N-acetyl-benzylamino]benzyl]-benzimidazole and 1N sodium hydroxide solution in ethanol.
Sources & evidence
- ORD record
- ord-eaa9ca9cd3f54d53a8577a36a102f607
- Source dataset
- uspto-grants-1996_05
- Patent number
- US05519138
Reaction notes
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