p-Toluenesulfonic acid monohydrate → 7-Bromo-2-tert-butyl-6-iodo-5-methyl-1,3-benzoxazole-4-carbonitrile

HRID 17266

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HRID 17266 반응식
O.C1(C)C=CC(S(O)(=O)=O)=CC=1.[Br:13][C:14]1[C:15]([OH:31])=[C:16]([NH:24][C:25](=O)[C:26]([CH3:29])([CH3:28])[CH3:27])[C:17]([C:22]#[N:23])=[C:18]([CH3:21])[C:19]=1[I:20].O.C(=O)(O)[O-].[Na+]>C1(C)C=CC=CC=1>[Br:13][C:14]1[C:19]([I:20])=[C:18]([CH3:21])[C:17]([C:22]#[N:23])=[C:16]2[C:15]=1[O:31][C:25]([C:26]([CH3:27])([CH3:28])[CH3:29])=[N:24]2

참가 물질

5

실험 절차

Toluene (25 ml), p-toluenesulfonic acid monohydrate (10.9 mg, 57.2 μmol) were added to N-(3-bromo-6-cyano-2-hydroxy-4-iodo-5-methylphenyl)-2,2-dimethylpropionamide (I-7) (250 mg, 572 μmol), followed by refluxing with a Dean-Stark condenser for 3 hours. After cooling, saturated sodium bicarbonate water (30 ml) was added to the reaction liquid, the product was extracted with ethyl acetate (50 ml×2). The organic layer was washed with saturated brine (50 ml), dried over anhydrous magnesium sulfate, concentrated under reduced pressure, the residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=6:1) to obtain the entitled compound (225 mg, 94%) as a pale yellow solid.

후처리

  1. temperatureby refluxing with a Dean-Stark condenser for 3 hours
  2. temperatureAfter cooling
  3. extractionthe product was extracted with ethyl acetate (50 ml×2)
  4. washThe organic layer was washed with saturated brine (50 ml)
  5. dry with materialdried over anhydrous magnesium sulfate
  6. concentrationconcentrated under reduced pressure
  7. customthe residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=6:1)

출처 및 근거

ORD 기록
ord-d082ca65db004cb3a7b902cc333cd858
출처 데이터셋
uspto-grants-2010_06
특허 번호
US07737166B2

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