4-Chloro-3-nitrobenzoic acid → 2-[2-[2-(4-Chlorophenyl)-5-methoxy-phenyl]-6-quinolyl]-1-(cyclopropylmethyl)benzimidazole-5-carboxylic acid

HRID 1788562Notes

Reaction equation

HRID 1788562 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.C1(CN)CC1.[Cl:19][C:20]1[CH:57]=[CH:56][C:23]([C:24]2[C:29]([C:30]3[CH:39]=[CH:38][C:37]4[C:32](=[CH:33][CH:34]=[C:35]([C:40]5[N:44](CC)[C:43]6C=C[C:49](C(O)=O)=[CH:50][C:42]=6N=5)[CH:36]=4)[N:31]=3)=[CH:28][C:27]([O:54][CH3:55])=[CH:26][CH:25]=2)=[CH:22][CH:21]=1>>[Cl:19][C:20]1[CH:57]=[CH:56][C:23]([C:24]2[C:29]([C:30]3[CH:39]=[CH:38][C:37]4[C:32](=[CH:33][CH:34]=[C:35]([C:40]5[N:44]([CH2:43][CH:42]6[CH2:50][CH2:49]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:36]=4)[N:31]=3)=[CH:28][C:27]([O:54][CH3:55])=[CH:26][CH:25]=2)=[CH:22][CH:21]=1

Participants

4

Procedure

The title compound was prepared from Resin 534a and cyclopropylmethylamine according to the procedure described in the preparation of Compound 534.

Sources & evidence

ORD record
ord-4a3c1138f892438db2fb90c0ff35dc06
Source dataset
uspto-grants-2009_03
Patent number
US07511145B2

Reaction notes

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