N-(2-(Aminomethyl)phenyl)-N-methylmethanesulfonamide → N-(2-(((6-Chloro-1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazolo[4,3-c]pyridin-4-yl)amino)methyl)phenyl)-N-methylmethanesulfonamide
Reaction equation
[Cl:1][c:2]1[n:16][c:15](Cl)[c:5]2[c:4]([n:8]([CH:9]3[O:14][CH2:13][CH2:12][CH2:11][CH2:10]3)[n:7][cH:6]2)[cH:3]1.[CH3:17][N:18]([S:27]([CH3:30])(=[O:29])=[O:28])[c:19]1[c:24]([CH2:25][NH2:26])[cH:23][cH:22][cH:21][cH:20]1>>[CH3:17][N:18]([S:27]([CH3:30])(=[O:29])=[O:28])[c:19]1[c:24]([CH2:25][NH:26][c:15]2[c:5]3[c:4]([n:8]([CH:9]4[O:14][CH2:13][CH2:12][CH2:11][CH2:10]4)[n:7][cH:6]3)[cH:3][c:2]([Cl:1])[n:16]2)[cH:23][cH:22][cH:21][cH:20]1Participants
6
Reactant 2
Product 1
Reagents, catalysts & solvents 3
Conditions
- Temperature
- 50 °C
Sources & evidence
- ORD record
- ord-9243553d83c345bebcb949b116290f6f
- Source dataset
- 39k HTE dataset from Pfizer
- Original link
- View source
Reaction notes
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