4-Methoxybenzylamine → N-Cyclopropyl-4-methyl-3-{1-[2-({[4-(methyloxy)phenyl]methyl}amino)-2-oxoethyl]-1H-indazol-5-yl}benzamide

HRID 1988941Notes

Reaction equation

HRID 1988941 reaction equation
[CH:1]1([NH:4][C:5]([C:7]2[CH:8]=[CH:9][C:10]([CH3:27])=[C:11]([C:13]3[CH:14]=[C:15]4[C:19](=[CH:20][CH:21]=3)[N:18]([CH2:22][C:23](OC)=[O:24])[N:17]=[CH:16]4)[CH:12]=2)=[O:6])[CH2:3][CH2:2]1.[CH3:28][O:29][C:30]1[CH:37]=[CH:36][C:33]([CH2:34][NH2:35])=[CH:32][CH:31]=1>>[CH:1]1([NH:4][C:5](=[O:6])[C:7]2[CH:8]=[CH:9][C:10]([CH3:27])=[C:11]([C:13]3[CH:21]=[C:20]4[C:19](=[CH:15][CH:14]=3)[N:18]([CH2:22][C:23]([NH:35][CH2:34][C:33]3[CH:36]=[CH:37][C:30]([O:29][CH3:28])=[CH:31][CH:32]=3)=[O:24])[N:17]=[CH:16]4)[CH:12]=2)[CH2:2][CH2:3]1

Participants

3

Reactant 2

HCID 754524-MethoxybenzylamineHCID 58656497HCID 58656497, compound

Product 1

HCID 58656476N-Cyclopropyl-4-methyl-3-{1-[2-({[4-(methyloxy)phenyl]methyl}amino)-2-oxoethyl]-1H-indazol-5-yl}benzamide

Procedure

Example 124 was prepared by General Method D using methyl (5-{5-[(cyclopropylamino)carbonyl]-2-methylphenyl}-1H-indazol-1-yl)acetate (Example 117) and 4-methoxybenzylamine to give the title compound (0.011 g).

Workup

  1. customExample 124 was prepared by General Method D

Sources & evidence

ORD record
ord-2dded45fcb03432291bc7b2cd68cab71
Source dataset
uspto-grants-2010_01
Patent number
US07642276B2

Reaction notes

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