Potassium Hydroxide → HCID 59191240, compound
Reaction equation
CS([O:5][C:6]1[CH:11]=[C:10]([CH2:12][CH2:13][CH3:14])[CH:9]=[CH:8][C:7]=1[O:15][C:16]1[CH:17]=[N:18][C:19]([NH:22][S:23]([CH3:26])(=[O:25])=[O:24])=[CH:20][CH:21]=1)(=O)=O.[OH-].[K+]>O>[OH:5][C:6]1[CH:11]=[C:10]([CH2:12][CH2:13][CH3:14])[CH:9]=[CH:8][C:7]=1[O:15][C:16]1[CH:21]=[CH:20][C:19]([NH:22][S:23]([CH3:26])(=[O:24])=[O:25])=[N:18][CH:17]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of 2-({6-[(methylsulfonyl)amino]pyridin-3-yl}oxy)-5-propylphenyl methanesulfonate (0.09 mmol; 30 mg), under argon, in water (0.5 mL), was added KOH (0.26 mmol; 15 mg). The reaction mixture was refluxed for 4 hr. After quenching with NH4Cl (1 mL), extraction with ethyl acetate (3*3 mL), combined organic phases were washed with water (3 mL), dried over MgSO4, concentrated in vacuo, to yield the title compound as a white solid (37 mg; 0.09 mmol; 77%).
Workup
- temperatureThe reaction mixture was refluxed for 4 hr
- customAfter quenching with NH4Cl (1 mL), extraction with ethyl acetate (3*3 mL)
- washwere washed with water (3 mL)
- dry with materialdried over MgSO4
- concentrationconcentrated in vacuo
Sources & evidence
- ORD record
- ord-ecda863ff2a9425c8262518f6bb9df2f
- Source dataset
- uspto-grants-2014_05
- Patent number
- US08722746B2
Reaction notes
Loading…