Trifluoroacetic acid → HCID 19921318, compound
Reaction equation
C(OC([NH:8][C:9]1([C:12]2[CH:17]=[CH:16][C:15]([C:18]3[N:22]([CH3:23])[C:21]4[CH:24]=[CH:25][C:26]([C:28]([NH:30][CH2:31][CH2:32][C:33]([O:35][CH3:36])=[O:34])=[O:29])=[CH:27][C:20]=4[N:19]=3)=[CH:14][CH:13]=2)[CH2:11][CH2:10]1)=O)(C)(C)C.FC(F)(F)C(O)=O>C(Cl)Cl>[NH2:8][C:9]1([C:12]2[CH:17]=[CH:16][C:15]([C:18]3[N:22]([CH3:23])[C:21]4[CH:24]=[CH:25][C:26]([C:28]([NH:30][CH2:31][CH2:32][C:33]([O:35][CH3:36])=[O:34])=[O:29])=[CH:27][C:20]=4[N:19]=3)=[CH:14][CH:13]=2)[CH2:10][CH2:11]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Prepared from 2-[4-(1-tert.butyloxycarbonylamino-cyclopropyl)-phenyl]-5-[(2-methoxycarbonyl-ethyl)-aminocarbonyl]-1-methyl-benzimidazole by treating with trifluoroacetic acid in methylene chloride at ambient temperature.
Sources & evidence
- ORD record
- ord-22b44ac5390c4b12a413e9596fdedffe
- Source dataset
- uspto-grants-1995_07
- Patent number
- US05434150
Reaction notes
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