Potassium Permanganate → 5-(4,6-Dimethoxypyrimidin-2-yl)oxy-3-methylbenzothiophene-4-carboxylic acid

HRID 51994노트

반응식

HRID 51994 반응식
[CH3:1][O:2][C:3]1[CH:8]=[C:7]([O:9][CH3:10])[N:6]=[C:5]([O:11][C:12]2[CH:13]=[CH:14][C:15]3[S:19][CH:18]=[C:17]([CH3:20])[C:16]=3[C:21]=2[CH:22]=[O:23])[N:4]=1.[Mn]([O-])(=O)(=O)=[O:25].[K+]>CC(C)=O.O>[CH3:10][O:9][C:7]1[CH:8]=[C:3]([O:2][CH3:1])[N:4]=[C:5]([O:11][C:12]2[C:21]([C:22]([OH:25])=[O:23])=[C:16]3[C:17]([CH3:20])=[CH:18][S:19][C:15]3=[CH:14][CH:13]=2)[N:6]=1

참가 물질

5

실험 절차

0.6 g of 5-(4,6-dimethoxypyrimidin-2-yl)oxy-4-formyl-3-methylbenzothiophene was dissolved in 80 ml of acetone. While stirring the solution at room temperature, 0.6 g of potassium permanganate dissolved in 10 ml of water was dropwise added thereto over a period of 15 minutes, and the mixture was further stirred at room temperature for 4 hours. It was then concentrated under reduced pressure to remove acetone, and then a saturated sodium bicarbonate aqueous solution was added thereto to make the mixture alkaline. The mixture was extracted with ethyl acetate, and then the aqueous layer was precipitated with 10% hydrochloric acid. The precipitated crystals were collected by filtration and washed with water to obtain 0.47 g (yield: 76%) of the desired compound.

후처리

  1. additionwas dropwise added
  2. stirringthe mixture was further stirred at room temperature for 4 hours
  3. concentrationIt was then concentrated under reduced pressure
  4. customto remove acetone
  5. additiona saturated sodium bicarbonate aqueous solution was added
  6. extractionThe mixture was extracted with ethyl acetate
  7. customthe aqueous layer was precipitated with 10% hydrochloric acid
  8. filtrationThe precipitated crystals were collected by filtration
  9. washwashed with water

출처 및 근거

ORD 기록
ord-f7bdde7295d34614a571b2a077a7bc7d
출처 데이터셋
uspto-grants-1997_04
특허 번호
US05616537

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