Acetic Acid → 2-(2-Fluoro4-(2-nitro-ethyl)-phenoxymethyl)pyridine

HRID 640339노트

반응식

HRID 640339 반응식
CS(C)=O.[F:5][C:6]1[CH:19]=[C:18](/[CH:20]=[CH:21]/[N+:22]([O-:24])=[O:23])[CH:17]=[CH:16][C:7]=1[O:8][CH2:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][N:11]=1.C(O)(=O)C.[BH4-].[Na+]>O>[F:5][C:6]1[CH:19]=[C:18]([CH2:20][CH2:21][N+:22]([O-:24])=[O:23])[CH:17]=[CH:16][C:7]=1[O:8][CH2:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][N:11]=1

참가 물질

6

실험 절차

To a dimethyl sulfoxide (30.0 mL) solution of 2-(2-fluoro-4-((E)-2-nitro-vinyl)-phenoxymethyl)-pyridine (3.00 g, 10.9 mmol) described in Manufacturing Example 87-1-2 and acetic acid (3.00 mL) was added sodium borohydride (660 mg, 17.4 mmol) at room temperature while cooling appropriately under nitrogen atmosphere, which was stirred for 20 minutes at room temperature. Water was then added dropwise at room temperature while cooling appropriately. The reaction mixture was extracted with ethyl acetate, and the organic layer was washed with water and saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated under a reduced pressure, and the residue was crystallized with a tetrahydrofuran-ethyl acetate-heptane system and filtered to obtain the title compound (1.50 g, 49.8%).

후처리

  1. temperaturewhile cooling appropriately under nitrogen atmosphere
  2. temperaturewhile cooling appropriately
  3. extractionThe reaction mixture was extracted with ethyl acetate
  4. washthe organic layer was washed with water and saturated aqueous sodium chloride
  5. dry with materialdried over anhydrous magnesium sulfate
  6. filtrationfiltered
  7. concentrationThe filtrate was concentrated under a reduced pressure
  8. customthe residue was crystallized with a tetrahydrofuran-ethyl acetate-heptane system
  9. filtrationfiltered

출처 및 근거

ORD 기록
ord-5caf64b3d26540eab29c4e27dc6eb4ec
출처 데이터셋
uspto-grants-2010_04
특허 번호
US07691882B2

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