Sodium hydroxide ethanol → HCID 15017904, compound
Reaction equation
[CH2:1]([C:5]1[N:9]([C:10]2[C:11]([CH3:25])=[C:12](C([O-])=O)[C:13](C3C=CC=CC=3)=[CH:14][CH:15]=2)[C:8]2[CH:26]=[CH:27][C:28]([C:30](=[O:37])[CH:31]([CH2:33][C:34]([OH:36])=[O:35])[CH3:32])=[CH:29][C:7]=2[N:6]=1)[CH2:2][CH2:3][CH3:4].[OH-:38].[Na+].[CH2:40]([OH:42])[CH3:41]>>[CH2:1]([C:5]1[N:9]([CH2:10][C:15]2[CH:25]=[CH:11][C:12]([C:4]3[C:41]([C:40]([OH:42])=[O:38])=[CH:5][CH:1]=[CH:2][CH:3]=3)=[CH:13][CH:14]=2)[C:8]2[CH:26]=[CH:27][C:28]([C:30](=[O:37])[CH:31]([CH2:33][C:34]([OH:36])=[O:35])[CH3:32])=[CH:29][C:7]=2[N:6]=1)[CH2:2][CH2:3][CH3:4]Participants
3
Procedure
Prepared is analogous manner to Example 72 from methyl 4'-[(2-n-butyl-5-(2-carboxymethyl-propionyl)-benzimidazol-1-yl(-methyl]biphenyl-2-carboxylate and aquous sodium hydroxide/ethanol.
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-2141307e01aa483ea62f3537b0550a84
- Source dataset
- uspto-grants-1999_01
- Patent number
- US05864043
Reaction notes
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