Hydroxylamine → N-Hydroxy-3-methanesulfonylbenzene-1-sulfonamide

HRID 1749191노트

반응식

HRID 1749191 반응식
[NH2:1][OH:2].O.[CH3:4][S:5]([C:8]1[CH:9]=[C:10]([S:14](Cl)(=[O:16])=[O:15])[CH:11]=[CH:12][CH:13]=1)(=[O:7])=[O:6].S(Cl)(Cl)(=O)=O>C1COCC1.C(Cl)Cl>[OH:2][NH:1][S:14]([C:10]1[CH:11]=[CH:12][CH:13]=[C:8]([S:5]([CH3:4])(=[O:7])=[O:6])[CH:9]=1)(=[O:16])=[O:15]

참가 물질

7

실험 절차

To a solution of aqueous hydroxylamine (16 mL of a 50% aqueous solution, 245 mmol) in THF (150 mL) and water (25 mL) cooled to −5° C. was slowly added 3-methanesulfonylbenzene-1-sulfonyl chloride (25 g, 98 mmol) while maintaining a reaction temperature of less than 10° C. The reaction was maintained at this temperature until substantially complete consumption of the sulfonyl chloride was observed (about 5 min), after which time the reaction was diluted with DCM (250 mL), the organic portion was separated and washed twice with 50 mL of water. The aqueous extracts were combined and rewashed twice with DCM (250 mL for each wash). All of the organic portions were combined, dried over sodium sulfate, filtered and concentrated under reduced pressure to provide the title compound as a beige solid. Trituration was carried out using heptanes:EtOAc (1:1; v:v) to provide the title compound as a beige solid (14 g, yield 56%). LC-MS tR=0.90 min; High Resolution Mass Spectroscopy (HRMS): theoretical (C7H9NO5S2)=249.9844, measured=249.9833; 1H NMR (500 MHz, DMSO-d6) δ ppm 9.85 (2H, q, J=3.3 Hz), 8.31 (1H, t, J=1.6 Hz), 8.28 (1H, dt, J=7.8, 1.3 Hz), 8.14-8.19 (1H, m), 7.93 (1H, t, J=7.9 Hz), 3.32 (3H, s).

후처리

  1. temperaturewhile maintaining a reaction temperature of less than 10° C
  2. custom(about 5 min)
  3. customthe organic portion was separated
  4. washwashed twice with 50 mL of water
  5. washeach wash)
  6. dry with materialdried over sodium sulfate
  7. filtrationfiltered
  8. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-0b0c6e79e57949a5b75c7233cc472001
출처 데이터셋
uspto-grants-2015_10
특허 번호
US09156804B2

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