3-ethynyl-4-methyl-N-(4-((4-methylpiperazin-1-yl)methyl)-3-(trifluoromethyl)phenyl)benzamide → 3-{[5-(2-amino-2-oxoethyl)pyrazin-2-yl]ethynyl}-4-methyl-N-{4-[(4-methylpiperazin-1-yl)methyl]-3-(trifluoromethyl)phenyl}benzamide
Reaction equation
Br[C:2]1[N:3]=[CH:4][C:5]([CH2:8][C:9]([NH2:11])=[O:10])=[N:6][CH:7]=1.[C:12]([C:14]1[CH:15]=[C:16]([CH:38]=[CH:39][C:40]=1[CH3:41])[C:17]([NH:19][C:20]1[CH:25]=[CH:24][C:23]([CH2:26][N:27]2[CH2:32][CH2:31][N:30]([CH3:33])[CH2:29][CH2:28]2)=[C:22]([C:34]([F:37])([F:36])[F:35])[CH:21]=1)=[O:18])#[CH:13]>>[NH2:11][C:9](=[O:10])[CH2:8][C:5]1[N:6]=[CH:7][C:2]([C:13]#[C:12][C:14]2[CH:15]=[C:16]([CH:38]=[CH:39][C:40]=2[CH3:41])[C:17]([NH:19][C:20]2[CH:25]=[CH:24][C:23]([CH2:26][N:27]3[CH2:28][CH2:29][N:30]([CH3:33])[CH2:31][CH2:32]3)=[C:22]([C:34]([F:35])([F:37])[F:36])[CH:21]=2)=[O:18])=[N:3][CH:4]=1Participants
3
Reactant 2
Product 1
Procedure
The title compound can be prepared as for example 1 using 2-(5-bromopyrazin-2-yl)acetamide and 3-ethynyl-4-methyl-N-{4-(4-methyl-piperazin-1-ylmethyl)-3-trifluoromethyl-phenyl}-benzamide.
Sources & evidence
- ORD record
- ord-83dc0755cfb94ebe8774f54d4214af25
- Source dataset
- uspto-grants-2013_06
- Patent number
- US08461167B2
Reaction notes
Loading…