N-(3-(trifluoromethyl)benzyl)-2-(5-(bis(2-methoxyethyl)amino)-2-nitrophenyl)isonicotinamide → N-(3-(trifluoromethyl)benzyl)-2-(2-amino-5-(bis(2-methoxyethyl)-amino)phenyl)isonicotinamide
Reaction equation
[F:1][C:2]([F:38])([F:37])[C:3]1[CH:4]=[C:5]([CH:34]=[CH:35][CH:36]=1)[CH2:6][NH:7][C:8](=[O:33])[C:9]1[CH:14]=[CH:13][N:12]=[C:11]([C:15]2[CH:20]=[C:19]([N:21]([CH2:26][CH2:27][O:28][CH3:29])[CH2:22][CH2:23][O:24][CH3:25])[CH:18]=[CH:17][C:16]=2[N+:30]([O-])=O)[CH:10]=1>CO.[Pd]>[F:37][C:2]([F:1])([F:38])[C:3]1[CH:4]=[C:5]([CH:34]=[CH:35][CH:36]=1)[CH2:6][NH:7][C:8](=[O:33])[C:9]1[CH:14]=[CH:13][N:12]=[C:11]([C:15]2[CH:20]=[C:19]([N:21]([CH2:22][CH2:23][O:24][CH3:25])[CH2:26][CH2:27][O:28][CH3:29])[CH:18]=[CH:17][C:16]=2[NH2:30])[CH:10]=1Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
Into a 50-mL round bottom flask, was placed a solution of N-(3-(trifluoromethyl)benzyl)-2-(5-(bis(2-methoxyethyl)amino)-2-nitrophenyl)-isonicotinamide (270 mg, 0.51 mmol, 1.00 equiv) in methanol (10 mL). The solution was treated with Pd/C (300 mg), and stirred under an atmosphere of hydrogen for 2 h at room temperature in a water bath. The solids were filtered out. The resulting mixture was concentrated under vacuum to yield 180 mg (71%) of product as a yellow to green oil.
Workup
- customInto a 50-mL round bottom flask, was placed
- filtrationThe solids were filtered out
- concentrationThe resulting mixture was concentrated under vacuum
Sources & evidence
- ORD record
- ord-59bd8c73b00d4420b47aa660c1fda0af
- Source dataset
- uspto-grants-2014_12
- Patent number
- US08916569B2
Reaction notes
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