Benzenesulfonyl chloride → 6-Chloro-1-phenylsulfonylindole

HRID 352767노트

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HRID 352767 반응식
C([Li])CCC.CCCCCC.[Cl:12][C:13]1[CH:21]=[C:20]2[C:16]([CH:17]=[CH:18][NH:19]2)=[CH:15][CH:14]=1.[C:22]1([S:28](Cl)(=[O:30])=[O:29])[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1>O1CCCC1.O>[Cl:12][C:13]1[CH:21]=[C:20]2[C:16]([CH:17]=[CH:18][N:19]2[S:28]([C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=2)(=[O:30])=[O:29])=[CH:15][CH:14]=1

참가 물질

7

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온도
-40 °C

실험 절차

At −78° C., n-butyl lithium (a 1.61M hexane solution, 3.34 ml) was added to a solution of 6-chloroindole (777 mg) in tetrahydrofuran (25 ml), followed by heating to −40° C. over 1 hour. The reaction mixture was cooled back to −78° C. and added with benzenesulfonyl chloride (867 μl). The resulting mixture was heated to room temperature over 3 hours. Water was added to the reaction mixture, followed by extraction with dichloromethane. The organic layers were combined, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by chromatography on a silica gel column (40 g of silica gel, hexane:ethyl acetate=5:7). The white solid so obtained was recrystallized from ethanol, whereby the title compound (826 mg, 55%) was obtained as a white solid.

후처리

  1. temperatureThe reaction mixture was cooled back to −78° C.
  2. temperatureThe resulting mixture was heated to room temperature over 3 hours
  3. extractionfollowed by extraction with dichloromethane
  4. dry with materialdried over anhydrous sodium sulfate
  5. concentrationconcentrated under reduced pressure
  6. customThe residue was purified by chromatography on a silica gel column (40 g of silica gel, hexane:ethyl acetate=5:7)
  7. customThe white solid so obtained
  8. customwas recrystallized from ethanol, whereby the title compound (826 mg, 55%)
  9. customwas obtained as a white solid

출처 및 근거

ORD 기록
ord-6226b0b864144981946253a112647c1f
출처 데이터셋
uspto-grants-2004_06
특허 번호
US06747023B1

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