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Melatonin → Melatonin Impurity 3

HRID 370057
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HRID 370057 반응식
[C:1](OC(=O)C)(=[O:3])[CH3:2].[CH3:8][C:9]([NH:11][CH2:12][CH2:13][C:14]1[C:18]2[CH:19]=[C:20]([O:23][CH3:24])[CH:21]=[CH:22][C:17]=2[NH:16][CH:15]=1)=[O:10]>C1C=CC=CC=1>[CH3:24][O:23][C:20]1[CH:19]=[C:18]2[C:17](=[CH:22][CH:21]=1)[NH:16][CH:15]=[C:14]2[CH2:13][CH2:12][N:11]([C:1]([CH3:2])=[O:3])[C:9](=[O:10])[CH3:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 896MelatoninHCID 7918Acetic Anhydride

생성물 1

HCID 832313Melatonin Impurity 3수율 50%

시약·촉매·용매 1

HCID 241Benzene용매2회

실험 절차

Acetic anhydride (7 ml) is added with stirring to melatonin (500 mg) dissolved in benzene (50 ml). The mixture is heated for 72 h in refluxing benzene. The solvent is evaporated off and the crude product is taken up in water and then neutralized with sodium carbonate solution (pH>8). After extraction (dichloromethane), washing (water) and drying (magnesium sulphate), the crude product is flash-chromatographed (EtOAc eluent). N-[2-(5-Methoxyindol-3-yl)ethyl]diacetamide (4) (300 mg, 50% yield) is obtained.

후처리

  1. temperatureThe mixture is heated for 72 h
  2. customThe solvent is evaporated off
  3. extractionAfter extraction (dichloromethane)
  4. washwashing (water)
  5. dry with materialdrying (magnesium sulphate)
  6. customthe crude product is flash-chromatographed (EtOAc eluent)

출처 및 근거

ORD 기록
ord-8a236f1593674321bb6c343b8c23bcb0
출처 데이터셋
uspto-grants-2000_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06140372

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