Sodium Thiosulfate → 1-{2-(2,4-difluorophenyl)-3,3-difluoro-2-methoxy-3-[(2-methoxyethyl)sulfonyl]propyl}-1H-1,2,4-triazole

HRID 613399노트

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HRID 613399 반응식
[F:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[C:9]([O:24][CH3:25])([C:16]([F:23])([F:22])SCCOC)[CH2:10][N:11]1[CH:15]=[N:14][CH:13]=[N:12]1.ClC1C=CC=[C:29]([C:33]([O:35]O)=O)C=1.[S:37]([O-:41])([O-])(=[O:39])=S.[Na+].[Na+].[C:44](=O)(O)[O-].[Na+]>ClCCl>[F:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[C:9]([O:24][CH3:25])([C:16]([F:23])([F:22])[S:37]([CH2:29][CH2:33][O:35][CH3:44])(=[O:41])=[O:39])[CH2:10][N:11]1[CH:15]=[N:14][CH:13]=[N:12]1

참가 물질

6

실험 절차

To a solution of 1-{2-(2,4-difluorophenyl)-3,3-difluoro-2-methoxy-3-[(2-methoxyethyl)thio]propyl}-1H-1,2,4-triazole (800 mg, 2.12 mmol) in dichloromethane (10 ml), 85% m-chloroperbenzoic acid (1.25 g, 5.09 mmol) was added at room temperature, followed by stirring at room temperature for 3 hours. After the completion of the reaction, a saturated aqueous solution of sodium thiosulfate and a saturated aqueous solution of sodium bicarbonate were added to the reaction mixture and the resulting mixture was stirred. The dichloromethane solution was separated, washed with water, dried over magnesium sulfate and distilled off under reduced pressure. The residue so obtained was subjected to a silica gel column. From the chloroform elute fraction, 700 mg (yield: 81%) of 1-{2-(2,4-difluorophenyl)-3,3-difluoro-2-methoxy-3-[(2-methoxyethyl)sulfonyl]propyl}-1H-1,2,4-triazole were obtained as a yellow oil.

후처리

  1. customAfter the completion of the reaction
  2. stirringthe resulting mixture was stirred
  3. customThe dichloromethane solution was separated
  4. washwashed with water
  5. dry with materialdried over magnesium sulfate
  6. distillationdistilled off under reduced pressure
  7. customThe residue so obtained
  8. washFrom the chloroform elute fraction

출처 및 근거

ORD 기록
ord-07b0b89c2e294ab4b056c98eb78f01c2
출처 데이터셋
uspto-grants-1999_12
특허 번호
US06008239

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