Sodium Hydroxide → HCID 22405435, compound
Reaction equation
[CH2:1]([C:4]1[N:8]([CH2:9][C:10]2[CH:15]=[CH:14][C:13]([C:16]3[C:17]([C:22]([O:24]C)=[O:23])=[CH:18][CH:19]=[CH:20][CH:21]=3)=[CH:12][CH:11]=2)[C:7]2[CH:26]=[C:27]([NH:31][C:32]3[NH:33][CH:34]=[CH:35][C:36]=3[N+:37]([O-:39])=[O:38])[CH:28]=[C:29]([CH3:30])[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:15]=[CH:14][C:13]([C:16]3[C:17]([C:22]([OH:24])=[O:23])=[CH:18][CH:19]=[CH:20][CH:21]=3)=[CH:12][CH:11]=2)[C:7]2[CH:26]=[C:27]([NH:31][C:32]3[NH:33][CH:34]=[CH:35][C:36]=3[N+:37]([O-:39])=[O:38])[CH:28]=[C:29]([CH3:30])[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 1d from methyl 4'-[[2-n-propyl-4-methyl-6-[N-(3-nitro-pyrrol-2-yl)-amino]-1H-benzimidazol -1-yl]-methyl]-biphenyl-2-carboxylate and 2N sodium hydroxide solution in ethanol.
Sources & evidence
- ORD record
- ord-f376e1c12da94e51a512b76a08cf3552
- Source dataset
- uspto-grants-1996_05
- Patent number
- US05521177
Reaction notes
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