4-Chloro-3-nitrobenzoic acid → 2-[2-[2-(4-Chlorophenyl)-5-methoxy-phenyl]-6-quinolyl]-1-(tetrahydrofuran-2-ylmethyl)benzimidazole-5-carboxylic acid
Reaction equation
Cl[C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[CH:4][C:3]=1[N+:11]([O-])=O.C(N)C1OCCC1.[Cl:21][C:22]1[CH:59]=[CH:58][C:25]([C:26]2[C:31]([C:32]3[CH:41]=[CH:40][C:39]4[C:34](=[CH:35][CH:36]=[C:37]([C:42]5[N:46](CC)[C:45]6[CH:49]=[CH:50][C:51]([C:53]([OH:55])=O)=CC=6N=5)[CH:38]=4)[N:33]=3)=[CH:30][C:29]([O:56][CH3:57])=[CH:28][CH:27]=2)=[CH:24][CH:23]=1>>[Cl:21][C:22]1[CH:59]=[CH:58][C:25]([C:26]2[C:31]([C:32]3[CH:41]=[CH:40][C:39]4[C:34](=[CH:35][CH:36]=[C:37]([C:42]5[N:46]([CH2:45][CH:49]6[CH2:50][CH2:51][CH2:53][O:55]6)[C:2]6[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[CH:4][C:3]=6[N:11]=5)[CH:38]=4)[N:33]=3)=[CH:30][C:29]([O:56][CH3:57])=[CH:28][CH:27]=2)=[CH:24][CH:23]=1Participants
4
Reactant 3
Product 1
Procedure
The title compound was prepared from Resin 534a and tetrahydrofurfurylamine according to the procedure described in the preparation of Compound 534.
Sources & evidence
- ORD record
- ord-2b51835bb50f4ee2b859ce6fb63abef9
- Source dataset
- uspto-grants-2009_03
- Patent number
- US07511145B2
Reaction notes
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