4-(aminomethyl)-N-methylbenzamide → HCID 58656500, compound

HRID 1988944Notes

Reaction equation

HRID 1988944 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.[NH2:28][CH2:29][C:30]1[CH:39]=[CH:38][C:33]([C:34]([NH:36][CH3:37])=[O: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:14]=[C:15]4[C:19](=[CH:20][CH:21]=3)[N:18]([CH2:22][C:23]([NH:28][CH2:29][C:30]3[CH:31]=[CH:32][C:33]([C:34]([NH:36][CH3:37])=[O:35])=[CH:38][CH:39]=3)=[O:24])[N:17]=[CH:16]4)[CH:12]=2)[CH2:3][CH2:2]1

Participants

3

Procedure

Example 127 was prepared by General Method D using methyl (5-{5-[(cyclopropylamino)carbonyl]-2-methylphenyl}-1H-indazol-1-yl)acetate (Example 117) and 4-(aminomethyl)-N-methylbenzamide to give the title compound (0.005 g).

Workup

  1. customExample 127 was prepared by General Method D

Sources & evidence

ORD record
ord-f0e6753282554a66bfa5013f1b4d96c7
Source dataset
uspto-grants-2010_01
Patent number
US07642276B2

Reaction notes

Loading…