Water → Benzenesulfonamide

HRID 1063953노트

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HRID 1063953 반응식
Cl[C:2]1[CH:7]=[CH:6][C:5]([S:8]([NH:11]C2C=C(F)C=CC=2F)(=[O:10])=[O:9])=[CH:4][CH:3]=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.CC(OC(/N=N/C(OC(C)C)=O)=O)C.O>C1COCC1>[C:5]1([S:8]([NH2:11])(=[O:10])=[O:9])[CH:6]=[CH:7][CH:2]=[CH:3][CH:4]=1

참가 물질

6

반응물 4

HCID 962WaterHCID 11776TriphenylphosphineHCID 47884524-chloro-N-(2,5-difluorophenyl)benzenesulfonamideHCID 5363146Diisopropyl azodicarboxylate

생성물 1

HCID 7370Benzenesulfonamide수율 56%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

반응 조건

온도
22 °C

실험 절차

To a solution of 4-chloro-N-[5-fluoro-2-fluorophenyl]benzenesulfonamide (500 mg, 1.65 mmol), triphenylphosphine (909 mg, 3.47 mmol) and 5S-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-2-pentanol (719 mg, 3.30 mmol) in THF (7 mL) was added diisopropylazodicarboxylate (0.682 mL, 3.47 mol) dropwise at 0° C. under nitrogen. The resulting mixture was allowed to warm to 22° C. with stirring. Stirring was continued for a period of 12 h followed by the addition of 15 mL of H2O. The mixture was extracted with ether (3×15 mL). The combined organic extracts were washed with NaHCO3 and sat. brine. The organic phase was dried over Na2SO4, filtered, and concentrated under reduced pressure. Silica gel chromatography (1:5 ethyl acetate:hexanes) of the concentrate afforded 466 mg of 4-chloro-N-[5-fluoro-2-flurophenyl]-N-[(R)-1-methyl-4-[(1,1-dimethylethyl)-dimethylsilyl]oxy)butyl]benzene-sulfonamide as a yellow oil in 56% yield.

후처리

  1. stirringStirring
  2. extractionThe mixture was extracted with ether (3×15 mL)
  3. washThe combined organic extracts were washed with NaHCO3 and sat. brine
  4. dry with materialThe organic phase was dried over Na2SO4
  5. filtrationfiltered
  6. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-da74b361c71d40b2bb9b35811ff8a13b
출처 데이터셋
uspto-grants-2005_11
특허 번호
US06967196B1

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