Trifluoroacetic acid → HCID 15104360, compound
Reaction equation
[CH2:1]([C:5]1[N:9]([CH2:10][C:11]2[CH:16]=[CH:15][C:14]([C:17]3[C:18]([C:23]([O:25]C(C)(C)C)=[O:24])=[CH:19][CH:20]=[CH:21][CH:22]=3)=[CH:13][CH:12]=2)[C:8]2[CH:30]=[CH:31][C:32]([N:34]([CH3:39])[C:35](=[O:38])[CH2:36][CH3:37])=[CH:33][C:7]=2[N:6]=1)[CH2:2][CH2:3][CH3:4].FC(F)(F)C(O)=O>>[CH2:1]([C:5]1[N:9]([CH2:10][C:11]2[CH:16]=[CH:15][C:14]([C:17]3[C:18]([C:23]([OH:25])=[O:24])=[CH:19][CH:20]=[CH:21][CH:22]=3)=[CH:13][CH:12]=2)[C:8]2[CH:30]=[CH:31][C:32]([N:34]([CH3:39])[C:35](=[O:38])[CH2:36][CH3:37])=[CH:33][C:7]=2[N:6]=1)[CH2:2][CH2:3][CH3:4]Participants
3
Procedure
Prepared in analogous manner to Example 9 from tert.butyl 4'-[(2-n-butyl-5-(N-propanoyl-methylamino)-benzimidazol-1-yl)-methyl]biphenyl-2-carboxylate and trifluoroacetic acid.
Sources & evidence
- ORD record
- ord-e9c16ea26b1b42b09f0458cc7f0f4b8e
- Source dataset
- uspto-grants-1996_07
- Patent number
- US05541229
Reaction notes
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