Sodium Hydroxide → HCID 19921211, compound
Reaction equation
[C:1]([CH2:4][CH2:5][NH:6][C:7]([C:9]1[CH:33]=[CH:32][C:12]2[N:13]([CH3:31])[C:14]([C:16]3[CH:21]=[CH:20][C:19]([CH2:22][N:23](C)[C:24](=O)C(F)(F)F)=[CH:18][CH:17]=3)=[N:15][C:11]=2[CH:10]=1)=[O:8])([OH:3])=[O:2].[OH-].[Na+]>>[C:1]([CH2:4][CH2:5][NH:6][C:7]([C:9]1[CH:33]=[CH:32][C:12]2[N:13]([CH3:31])[C:14]([C:16]3[CH:17]=[CH:18][C:19]([CH2:22][NH:23][CH3:24])=[CH:20][CH:21]=3)=[N:15][C:11]=2[CH:10]=1)=[O:8])([OH:3])=[O:2]Participants
3
Procedure
Prepared from 5-[(2-carboxy-ethyl)-aminocarbonyl]-1-methyl-2-[4-(N-trifluoroacetyl-methylaminomethyl)-phenyl]-benzimidazole by treating with 2N sodium hydroxide solution.
Sources & evidence
- ORD record
- ord-c1c41f518e2d429295fbc05b090f226d
- Source dataset
- uspto-grants-1995_07
- Patent number
- US05434150
Reaction notes
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