2-Methoxyethylamine → HCID 76285397, compound
Reaction equation
[Cl:1][C:2]1[C:7]([O:8][CH3:9])=[CH:6][C:5]([O:10][CH3:11])=[C:4]([Cl:12])[C:3]=1[C:13]1[N:18]=[CH:17][C:16]2[C:19]([C:22]3[CH:23]=[N:24][N:25]([CH2:27][C:28](O)=[O:29])[CH:26]=3)=[N:20][NH:21][C:15]=2[CH:14]=1.[CH3:31][O:32][CH2:33][CH2:34][NH2:35]>>[Cl:1][C:2]1[C:7]([O:8][CH3:9])=[CH:6][C:5]([O:10][CH3:11])=[C:4]([Cl:12])[C:3]=1[C:13]1[N:18]=[CH:17][C:16]2[C:19]([C:22]3[CH:23]=[N:24][N:25]([CH2:27][C:28]([NH:35][CH2:34][CH2:33][O:32][CH3:31])=[O:29])[CH:26]=3)=[N:20][NH:21][C:15]=2[CH:14]=1Participants
3
Procedure
This compound was prepared by using procedures analogous to those described for the synthesis of Example 36, Step 2, starting from {4-[6-(2,6-dichloro-3,5-dimethoxyphenyl)-1H-pyrazolo[4,3-c]pyridin-3-yl]-1H-pyrazol-1-yl}acetic acid and 2-Methoxyethylamine. LCMS (M+H)+=505.1/507.1.
Workup
- customThis compound was prepared
- customthose described for the synthesis of Example 36, Step 2
Sources & evidence
- ORD record
- ord-c1f50017ea43441da85d88d1374bfc29
- Source dataset
- uspto-grants-2016_02
- Patent number
- US09266892B2
Reaction notes
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