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

HRID 2047937Notes

Reaction equation

HRID 2047937 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]=1

Participants

3

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

  1. extractionextracted twice with ethyl acetate
  2. washCombined organic layers were washed with saturated brine
  3. dry with materialdried over anhydrous magnesium sulfate
  4. concentrationconcentrated under reduced pressure

Sources & evidence

ORD record
ord-c21fd194fde74688948a4bdd3c96ff5c
Source dataset
uspto-grants-2013_11
Patent number
US08592597B2

Reaction notes

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