Acetic Acid → N-(2-Hydroxy-2-(4-isopropyl-2-methoxyphenyl)-5-nitro-1,3-dioxo-2,3-dihydro-1H-inden-4-yl)acetamide

HRID 527131

반응식

HRID 527131 반응식
O[C:2]1([OH:20])[C:10](=[O:11])[C:9]2[C:4](=[CH:5][CH:6]=[C:7]([N+:16]([O-:18])=[O:17])[C:8]=2[NH:12][C:13](=[O:15])[CH3:14])[C:3]1=[O:19].[Se]=O.CC(O)=O.[CH:27]([C:30]1[CH:35]=[CH:34][CH:33]=[C:32]([O:36][CH3:37])[CH:31]=1)([CH3:29])[CH3:28]>O1CCOCC1>[OH:20][C:2]1([C:33]2[CH:34]=[CH:35][C:30]([CH:27]([CH3:29])[CH3:28])=[CH:31][C:32]=2[O:36][CH3:37])[C:10](=[O:11])[C:9]2[C:4](=[CH:5][CH:6]=[C:7]([N+:16]([O-:18])=[O:17])[C:8]=2[NH:12][C:13](=[O:15])[CH3:14])[C:3]1=[O:19]

참가 물질

6

실험 절차

N-(2,2-dihydroxy-5-nitro-1,3-dioxo-2,3-dihydro-1H-inden-4-yl)acetamide (2.60 g, 11.1 mmol) was completely dissolved in anhydrous dioxane (20 ml). This solution was added with selenium oxide (2.70 g, 24.4 mmol) and AcOH (1.5 ml). The reaction mixture was heated for 7 hrs under reflux. After filtration at high temperature, the filtrate was concentrated to afford 1.79 g (100%). Trifluoroacetic solution of the resulting product was added with isopropyl-3-methoxybenzene (1.66 g, 11.1 mmol), followed by stirring for 12 hrs. The remainder was extracted with ethyl acetate, and concentrated organic layer was purified using column chromatography (ethylacetate 100%) to afford the title compound (0.64 g, 14%).

후처리

  1. temperatureThe reaction mixture was heated for 7 hrs
  2. temperatureunder reflux
  3. filtrationAfter filtration at high temperature
  4. concentrationthe filtrate was concentrated
  5. customto afford 1.79 g (100%)
  6. extractionThe remainder was extracted with ethyl acetate, and concentrated organic layer
  7. customwas purified

출처 및 근거

ORD 기록
ord-b9026bf2745a4c489f3604990c375759
출처 데이터셋
uspto-grants-2016_05
특허 번호
US09346749B2

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