5H-[1,3]Dioxolo[4,5-f]indole-6,7-dione → 3-(1-Methoxy-1-phenyl-methylidene)-5,6-methylenedioxy-2-indolinone

HRID 1007388노트

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HRID 1007388 반응식
C([C:3](CC)(P(=O)([O-])[O-])[C:4]1(OC)[CH:9]=[CH:8][CH:7]=[CH:6][CH2:5]1)C.C[C:19](C)([O-:21])C.[K+].[CH2:24]1[O:35][C:34]2[CH:33]=[C:32]3[C:28]([C:29](=O)[C:30](=[O:36])[NH:31]3)=[CH:27][C:26]=2[O:25]1>CN(C)C=O>[CH3:19][O:21][C:3](=[C:29]1[C:28]2[C:32](=[CH:33][C:34]3[O:35][CH2:24][O:25][C:26]=3[CH:27]=2)[NH:31][C:30]1=[O:36])[C:4]1[CH:5]=[CH:6][CH:7]=[CH:8][CH:9]=1

참가 물질

5

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온도
-10 °C

실험 절차

Under a nitrogen atmosphere 4.5 g of diethyl-1-methoxybenzylphosphonate (according to Burkhouse, D.; Zimmer, H.; Synthesis 1984, 330) are dissolved in 40 ml of absolute dimethylformamide and at −40° C. 4.0 g of potassium-tert-butoxide are added batchwise and stirred for 15 minutes at −10° C. 3.0 g of 5,6-methylenedioxyisatin (according to Lackey, K.; Sternbach, D. D.; Synthesis 1993, 993) are added to the clear solution and stirred for 1 hour at ambient temperature. After this time the mixture is poured into 20 ml of ice-cold saturated potassium hydrogen sulphate solution and extracted with ethyl acetate. The ethyl acetate phase is washed with water, dried over sodium sulphate and concentrated by evaporation. Finally the residue is separated through a silica gel column with toluene/ethyl acetate (5:1). The product obtained can be recrystallised from ether.

후처리

  1. stirringstirred for 1 hour at ambient temperature
  2. extractionextracted with ethyl acetate
  3. washThe ethyl acetate phase is washed with water
  4. dry with materialdried over sodium sulphate
  5. concentrationconcentrated by evaporation
  6. customFinally the residue is separated through a silica gel column with toluene/ethyl acetate (5:1)
  7. customThe product obtained can
  8. custombe recrystallised from ether

출처 및 근거

ORD 기록
ord-b2b46c844f114b12aaca447e40a18e13
출처 데이터셋
uspto-grants-2004_09
특허 번호
US06794395B1

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