Pyridine → N-(3-bromo-2,4-difluorophenyl)propane-1-sulfonamide

HRID 1889244Notes

Reaction equation

HRID 1889244 reaction equation
[Br:1][C:2]1[C:3]([F:10])=[C:4]([CH:6]=[CH:7][C:8]=1[F:9])[NH2:5].[CH2:11]([S:14](Cl)(=[O:16])=[O:15])[CH2:12][CH3:13].N1C=CC=CC=1.C(=O)(O)[O-].[Na+]>CN(C1C=CN=CC=1)C.C(Cl)Cl>[Br:1][C:2]1[C:3]([F:10])=[C:4]([NH:5][S:14]([CH2:11][CH2:12][CH3:13])(=[O:16])=[O:15])[CH:6]=[CH:7][C:8]=1[F:9]

Participants

7

Reactant 4

HCID 1049PyridineHCID 662791-Propanesulfonyl chlorideHCID 516892Sodium BicarbonateHCID 137327463-Bromo-2,4-difluoroaniline

Product 1

HCID 51034457N-(3-bromo-2,4-difluorophenyl)propane-1-sulfonamide

Reagents, catalysts & solvents 2

HCID 142844-(Dimethylamino)pyridineCatalystHCID 6344DichloromethaneSolvent

Procedure

A solution of 3-bromo-2,4-difluoroaniline (4.16 g, 20 mmol, EP184384), n-propanesulfonyl chloride (4.6 ml, 40 mmol), pyridine (8 ml), DMAP (97 mg), and DCM (100 ml) was stirred at rt for 16 h. Aqueous sodium bicarbonate solution was added and the mixture was extracted with ethyl acetate. The organic layer was washed with aqueous sodium bicarbonate and brine. The crude product was purified by silica gel chromatography (8:1 to 3:1 hexanes/ethyl acetate eluant) to give the title compound. MS m/z 313.9 (M+1).

Workup

  1. extractionthe mixture was extracted with ethyl acetate
  2. washThe organic layer was washed with aqueous sodium bicarbonate and brine
  3. customThe crude product was purified by silica gel chromatography (8:1 to 3:1 hexanes/ethyl acetate eluant)

Sources & evidence

ORD record
ord-5ddef47a8d8c4bf4b0bc1a5a0925faa4
Source dataset
uspto-grants-2013_08
Patent number
US08501758B2

Reaction notes

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