Methylamine → HCID 178482449, compound
Reaction equation
[CH3:1][NH2:2].Cl[C:4]1[C:22]([N+:23]([O-:25])=[O:24])=[CH:21][C:7]([C:8]([NH:10][C@H:11]2[CH2:16][CH2:15][C@H:14]([C:17]([F:20])([F:19])[F:18])[CH2:13][CH2:12]2)=[O:9])=[C:6]([O:26][CH2:27][CH2:28][O:29][CH3:30])[N:5]=1>C1COCC1.O>[CH3:30][O:29][CH2:28][CH2:27][O:26][C:6]1[N:5]=[C:4]([NH:2][CH3:1])[C:22]([N+:23]([O-:25])=[O:24])=[CH:21][C:7]=1[C:8]([NH:10][C@H:11]1[CH2:16][CH2:15][C@H:14]([C:17]([F:20])([F:19])[F:18])[CH2:13][CH2:12]1)=[O:9]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
Methylamine (2 M in THF; 400 μL, 0.80 mmol) is added to 6-chloro-2-(2-methoxy-ethoxy)-5-nitro-N-(trans-4-trifluoromethyl-cyclohexyl)-nicotinamide (150 mg, 0.35 mmol) in THF (10 mL). After 45 min at rt the reaction mixture is diluted with water, concentrated and filtered. The filtercake is washed with water and dried.
Workup
- concentrationconcentrated
- filtrationfiltered
- washThe filtercake is washed with water
- customdried
Sources & evidence
- ORD record
- ord-7c25da5ce18342c590f3839c9b30abac
- Source dataset
- uspto-grants-2013_11
- Patent number
- US08586604B2
Reaction notes
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