HCID 140409624, compound → HCID 140409614, compound
Reaction equation
[C:1]1([N:7]([CH2:40][CH2:41][CH2:42][O:43]CC2C=CC=CC=2)[C:8]([C:10]2[CH:39]=[CH:38][C:13]3[N:14]([CH3:37])[C:15]([CH2:17][NH:18][C:19]4[CH:24]=[CH:23][C:22]([C:25](=[NH:36])[NH:26][C:27]([O:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH3:35])=[O:28])=[CH:21][CH:20]=4)=[N:16][C:12]=3[CH:11]=2)=[O:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1>ClCCl.C(O)C>[C:1]1([N:7]([CH2:40][CH2:41][CH2:42][OH:43])[C:8]([C:10]2[CH:39]=[CH:38][C:13]3[N:14]([CH3:37])[C:15]([CH2:17][NH:18][C:19]4[CH:24]=[CH:23][C:22]([C:25](=[NH:36])[NH:26][C:27]([O:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH3:35])=[O:28])=[CH:21][CH:20]=4)=[N:16][C:12]=3[CH:11]=2)=[O:9])[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
Prepared analogously to Example 165 from 1-methyl-2-[N-[4-(N-n-hexyloxycarbonylamidino)phenyl]-aminomethyl]-benzimidazole-5-yl-carboxylic acid-N-phenyl-N-(3-benzyloxy-n-propyl)-amide by catalytic debenzylation. Yield: 26% of theory, C33H40N6O4 (584.7) Rf value: 0.39 (silica gel; dichloromethane/ethanol=9:1 ##EQU124##
Sources & evidence
- ORD record
- ord-4c25049cc58547ad807dd72deac20b87
- Source dataset
- uspto-grants-2000_07
- Patent number
- US06087380
Reaction notes
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