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Citric Acid → 2-(1,5-dimethyl-1H-indol-3-yl)-3-(5-methyl-1H-indol-3-yl)-N-methylmaleimide

HRID 1357104
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HRID 1357104 반응식
[CH3:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[NH:7][CH:6]=[CH:5]2.C([Mg]Br)C.Br[C:16]1[C:17]([N:19]([CH3:34])[C:20](=[O:33])[C:21]=1[C:22]1[C:30]2[C:25](=[CH:26][CH:27]=[C:28]([CH3:31])[CH:29]=2)[N:24]([CH3:32])[CH:23]=1)=[O:18].C(O)(=O)CC(CC(O)=O)(C(O)=O)O>C1(C)C=CC=CC=1>[CH3:32][N:24]1[C:25]2[C:30](=[CH:29][C:28]([CH3:31])=[CH:27][CH:26]=2)[C:22]([C:21]2[C:20]([N:19]([CH3:34])[C:17](=[O:18])[C:16]=2[C:5]2[C:4]3[C:8](=[CH:9][CH:10]=[C:2]([CH3:1])[CH:3]=3)[NH:7][CH:6]=2)=[O:33])=[CH:23]1
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참가 물질

6

반응물 4

HCID 311Citric AcidHCID 119785-MethylindoleHCID 185054442-bromo-3-(1,5-dimethyl-1H-indol-3-yl)-N-methylmaleimideHCID 178418443HCID 178418443, 화합물

생성물 1

HCID 185054452-(1,5-dimethyl-1H-indol-3-yl)-3-(5-methyl-1H-indol-3-yl)-N-methylmaleimide수율 86.9%

시약·촉매·용매 1

HCID 1140
Toluene
용매
2회

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온도
40 °C

실험 절차

To a solution of 5-methylindole (77 mg, 0.66 mmol) dissolved in toluene (1 mL) was added 0.95M ethylmagnesium bromide (0.7 mL, 0.66 mmol) at 40° C., and the whole was stirred at 40° C. for 45 minutes. Successively, a solution of 2-bromo-3-(1,5-dimethyl-1H-indol-3-yl)-N-methylmaleimide (100 mg, 0.3 mmol) dissolved in toluene (5 mL) was added thereto, followed by stirring under heating and refluxing for 3 hours. After 20% aqueous citric acid solution (1 mL) was added thereto under ice cooling and the whole was stirred, toluene was removed by concentration under reduced pressure and the resulting concentrate was extracted with ethyl acetate. The extract was dried over sodium sulfate and then concentrated under reduced pressure. The residue was purified by column chromatography over silica gel (ethyl acetate:n-hexane=1:2) to obtain 2-(1,5-dimethyl-1H-indol-3-yl)-3-(5-methyl-1H-indol-3-yl)-N-methylmaleimide (100 mg, 86.9%) as red solids.

후처리

  1. additionwas added
  2. stirringby stirring
  3. temperatureunder heating
  4. temperaturerefluxing for 3 hours
  5. stirringunder ice cooling and the whole was stirred
  6. customtoluene was removed by concentration under reduced pressure
  7. concentrationthe resulting concentrate
  8. extractionwas extracted with ethyl acetate
  9. dry with materialThe extract was dried over sodium sulfate
  10. concentrationconcentrated under reduced pressure
  11. customThe residue was purified by column chromatography over silica gel (ethyl acetate:n-hexane=1:2)

출처 및 근거

ORD 기록
ord-59e0ae62c50446379ec2d969abb3024f
출처 데이터셋
uspto-grants-2003_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06589977B1

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