p-(Trifluoromethoxy)phenyl isocyanate → HCID 46209419, compound
Reaction equation
[NH2:1][C:2]1[CH:3]=[C:4]([N:8]([CH3:24])[C:9]2[N:14]=[C:13]3[S:15][C:16]([NH:18][C:19]([CH:21]4[CH2:23][CH2:22]4)=[O:20])=[N:17][C:12]3=[CH:11][CH:10]=2)[CH:5]=[CH:6][CH:7]=1.[N:25]([C:28]1[CH:33]=[CH:32][C:31]([O:34][C:35]([F:38])([F:37])[F:36])=[CH:30][CH:29]=1)=[C:26]=[O:27].C(=O)([O-])O.[Na+]>CN(C)C=O>[CH3:24][N:8]([C:4]1[CH:5]=[CH:6][CH:7]=[C:2]([NH:1][C:26](=[O:27])[NH:25][C:28]2[CH:33]=[CH:32][C:31]([O:34][C:35]([F:36])([F:38])[F:37])=[CH:30][CH:29]=2)[CH:3]=1)[C:9]1[N:14]=[C:13]2[S:15][C:16]([NH:18][C:19]([CH:21]3[CH2:22][CH2:23]3)=[O:20])=[N:17][C:12]2=[CH:11][CH:10]=1Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of N-{5-[(3-aminophenyl)(methyl)amino][1,3]thiazolo[5,4-b]pyridin-2-yl}cyclopropanecarboxamide (100 mg, 0.295 mmol) produced in Example 8(x) in N,N-dimethylformamide (1.0 mL) was added 1-isocyanato-4-(trifluoromethoxy)benzene (53 μL, 0.354 mmol), and the mixture was stirred at room temperature for 1 hr. Aqueous sodium hydrogen carbonate solution (20 mL) was added to the reaction mixture, and the mixture was extracted with ethyl acetate (50 mL). The organic layer was washed with saturated brine (20 mL), dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The precipitate was collected by filtration, and recrystallized from hexane/tetrahydrofuran to give the title compound (101 mg, 63%) as a colorless powder.
Workup
- extractionthe mixture was extracted with ethyl acetate (50 mL)
- washThe organic layer was washed with saturated brine (20 mL)
- dry with materialdried over anhydrous sodium sulfate
- concentrationconcentrated under reduced pressure
- filtrationThe precipitate was collected by filtration
- customrecrystallized from hexane/tetrahydrofuran
Sources & evidence
- ORD record
- ord-6784343289114d5f898e09f1d816eebf
- Source dataset
- uspto-grants-2014_04
- Patent number
- US08697874B2
Reaction notes
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