Hydrochloric Acid → (R)-2-methyl-6-nitro-2,3-dihydroimidazo[2,1-b]oxazol-2-ylmethyl N-(4-chlorophenyl)-N-methylcarbamate

HRID 856187노트

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HRID 856187 반응식
I[CH3:2].[OH-].[K+].[Cl:5][C:6]1[CH:11]=[CH:10][C:9]([NH:12][C:13](=[O:29])[O:14][CH2:15][C@@:16]([OH:28])([CH3:27])[CH2:17][N:18]2[CH:22]=[C:21]([N+:23]([O-:25])=[O:24])[N:20]=[C:19]2Cl)=[CH:8][CH:7]=1.Cl>CS(C)=O>[Cl:5][C:6]1[CH:11]=[CH:10][C:9]([N:12]([CH3:2])[C:13](=[O:29])[O:14][CH2:15][C@:16]2([CH3:27])[O:28][C:19]3=[N:20][C:21]([N+:23]([O-:25])=[O:24])=[CH:22][N:18]3[CH2:17]2)=[CH:8][CH:7]=1

참가 물질

6

실험 절차

Iodomethane (0.71 ml, 11.4 mmol) and potassium hydroxide (0.64 g, 11.4 mmol) were added to a solution of (R)-3-(2-chloro-4-nitroimidazol-1-yl)-2-hydroxy-2-methylpropyl 4-chlorophenylcarbamate prepared in Example 64 (1.5 g, 3.8 mmol) in DMSO (40 ml) followed by stirring at room temperature for 4 hours. The mixture was cooled on ice-bath and added 10% hydrochloric acid. The resulting mixture was extracted with ethyl acetate, and the extract was washed with water, dried over magnesium sulfate and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography (n-hexane/ethyl acetate=1/1) and recrystallized from isopropanol to afford (R)-2-methyl-6-nitro-2,3-dihydroimidazo[2,1-b]oxazol-2-ylmethyl N-(4-chlorophenyl)-N-methylcarbamate (0.67 g, 60%) as a white solid.

후처리

  1. temperatureThe mixture was cooled on ice-bath
  2. extractionThe resulting mixture was extracted with ethyl acetate
  3. washthe extract was washed with water
  4. dry with materialdried over magnesium sulfate
  5. concentrationconcentrated under reduced pressure
  6. customThe residue was purified by silica gel column chromatography (n-hexane/ethyl acetate=1/1)
  7. customrecrystallized from isopropanol

출처 및 근거

ORD 기록
ord-4437f7db2a4d4ff9a4ad01db8a9346eb
출처 데이터셋
uspto-grants-2007_08
특허 번호
US07262212B2

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