Methyl iodide → HCID 57907565, 화합물

HRID 1888164노트

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HRID 1888164 반응식
[CH2:1]([CH:8]([N:12]1[CH2:16][CH2:15][O:14][C:13]1=[O:17])[C:9]([O-:11])=[O:10])C1C=CC=CC=1.[CH:18]([N-]C(C)C)([CH3:20])[CH3:19].[Li+].IC.[CH2:28]1[CH2:32]O[CH2:30][CH2:29]1>>[O:17]=[C:13]1[N:12]([CH:8]([CH3:1])[C:9]([O:11][CH2:30][C:29]2[CH:20]=[CH:18][CH:19]=[CH:32][CH:28]=2)=[O:10])[CH2:16][CH2:15][O:14]1

참가 물질

5

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온도
-78 °C

실험 절차

To a stirred solution of 0.50 g (2.1 mmol) of benzyl(2-oxo-1,3-oxazolidin-3-yl)acetate from step A in 15 mL of anhydrous THF at −78° C. under an atmosphere of nitrogen was added 1.2 mL (2.4 mmol) of a 2.0 M solution of lithium diisopropylamide in anhydrous THF. The resulting yellow solution was stirred for 15 min at −78° C. and then 0.0360 g (2.55 mmol) of iodomethane was added. The resulting mixture was stirred for 2 h with gradual warming to ambient temperature then quenched with a saturated aqueous ammonium chloride solution. The aqueous phase was extracted with ethyl acetate (3×20 mL) and the combined organics were washed with brine, dried over magnesium sulfate, filtered and evaporated to dryness in vacuo. The crude residue was purified by silica gel chromatography eluting with 40% ethyl acetate in hexanes to afford the title compound as a clear gum 0.37 g (70%). LC-MS: m/z (ES) 250 (MH)+.

후처리

  1. stirringThe resulting mixture was stirred for 2 h
  2. temperaturewith gradual warming to ambient temperature
  3. customthen quenched with a saturated aqueous ammonium chloride solution
  4. extractionThe aqueous phase was extracted with ethyl acetate (3×20 mL)
  5. washthe combined organics were washed with brine
  6. dry with materialdried over magnesium sulfate
  7. filtrationfiltered
  8. customevaporated to dryness in vacuo
  9. customThe crude residue was purified by silica gel chromatography
  10. washeluting with 40% ethyl acetate in hexanes

출처 및 근거

ORD 기록
ord-de01482c776e4be6b1adfb00721bd2ab
출처 데이터셋
uspto-grants-2013_08
특허 번호
US08501786B2

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