1-{4-Fluoro-5-(2-fluoropyridin-3-yl)-1-[(4-methylpyridin-2-yl)sulfonyl]-1H-pyrrol-3-yl}-N-methylmethanamine hydrochloride → 1-{4-Fluoro-5-(2-fluoropyridin-3-yl)-1-[(4-methylpyridin-2-yl)sulfonyl]-1H-pyrrol-3-yl}-N-methylmethanamine
Reaction equation
Cl.[F:2][C:3]1[C:4]([CH2:25][NH:26][CH3:27])=[CH:5][N:6]([S:15]([C:18]2[CH:23]=[C:22]([CH3:24])[CH:21]=[CH:20][N:19]=2)(=[O:17])=[O:16])[C:7]=1[C:8]1[C:9]([F:14])=[N:10][CH:11]=[CH:12][CH:13]=1>C(=O)([O-])O.[Na+]>[F:2][C:3]1[C:4]([CH2:25][NH:26][CH3:27])=[CH:5][N:6]([S:15]([C:18]2[CH:23]=[C:22]([CH3:24])[CH:21]=[CH:20][N:19]=2)(=[O:17])=[O:16])[C:7]=1[C:8]1[C:9]([F:14])=[N:10][CH:11]=[CH:12][CH:13]=1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
1-{4-Fluoro-5-(2-fluoropyridin-3-yl)-1-[(4-methylpyridin-2-yl)sulfonyl]-1H-pyrrol-3-yl}-N-methylmethanamine hydrochloride (751 mg) was dissolved in saturated aqueous sodium hydrogen carbonate, and extracted twice with ethyl acetate. Combined organic layers were washed with saturated brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure to give the title compound as a pale-yellow oil (yield 647 mg, 95%).
Workup
- extractionextracted twice with ethyl acetate
- washCombined organic layers were washed with saturated brine
- dry with materialdried over anhydrous magnesium sulfate
- concentrationconcentrated under reduced pressure
Sources & evidence
- ORD record
- ord-f65e581278354f37842a48218f6964ed
- Source dataset
- uspto-grants-2015_03
- Patent number
- US08969387B2
Reaction notes
Loading…