Sodium Hydroxide → HCID 53735396, compound
Reaction equation
[CH2:1]([C:4]1[N:8]([CH2:9][C:10]2[CH:15]=[CH:14][C:13]([O:16][CH:17]([C:25]([O:27]CC)=[O:26])[C:18]3[CH:23]=[CH:22][CH:21]=[CH:20][C:19]=3[Cl:24])=[CH:12][CH:11]=2)[C:7]2[CH:30]=[CH:31][CH:32]=[C:33]([CH3:34])[C:6]=2[N:5]=1)[CH2:2][CH3:3].[OH-].[Na+]>C(O)C>[CH2:1]([C:4]1[N:8]([CH2:9][C:10]2[CH:11]=[CH:12][C:13]([O:16][CH:17]([C:25]([OH:27])=[O:26])[C:18]3[CH:23]=[CH:22][CH:21]=[CH:20][C:19]=3[Cl:24])=[CH:14][CH:15]=2)[C:7]2[CH:30]=[CH:31][CH:32]=[C:33]([CH3:34])[C:6]=2[N:5]=1)[CH2:2][CH3:3]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Prepared analogously to Example 1b from 2-n-propyl-4-methyl-1-[4-[(α-ethoxycarbonyl)-2-chlorobenzyloxy]-benzyl]benzimidazole and 2N sodium hydroxide solution in ethanol.
Sources & evidence
- ORD record
- ord-3f788c30e9a443bbbee18477e1548db1
- Source dataset
- uspto-grants-1996_05
- Patent number
- US05519138
Reaction notes
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