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Methyl iodide → Methyl α-propoxy-1H-indole-5-propanoate

HRID 2181192
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HRID 2181192 반응식
[NH:1]1[C:9]2[C:4](=[CH:5][C:6]([CH2:10][CH:11]([O:15][CH2:16][CH2:17][CH3:18])[C:12]([OH:14])=[O:13])=[CH:7][CH:8]=2)[CH:3]=[CH:2]1.[C:19](=O)([O-])O.[Na+].CI>CN(C)C=O>[CH3:19][O:13][C:12](=[O:14])[CH:11]([O:15][CH2:16][CH2:17][CH3:18])[CH2:10][C:6]1[CH:5]=[C:4]2[C:9](=[CH:8][CH:7]=1)[NH:1][CH:2]=[CH:3]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6328Methyl iodideHCID 516892Sodium BicarbonateHCID 22485685HCID 22485685, 화합물

생성물 1

HCID 69562937Methyl α-propoxy-1H-indole-5-propanoate

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

Crude rac-3-(1H-indol-5-yl)-2-propoxy-propionic acid was dissolved in 5 ml N,N-dimethylformamide, 0.54 g of sodium hydrogencarbonate was added followed by 0.32 nm of methyl iodide. The mixture was stirred at r.t. for 7 hours, then poured into ice water and extracted 3 times with ethyl acetate; after drying over MgSO4 and evaporation, the crude product was purified by chromatograph) (silicagel, eluent: gradient of n-heptane/ethyl acetate) to yield 0.47 g of rac-3-(1H-indol-5-yl)-2-propoxy-propionic acid methyl ester as light yellow oil.

후처리

  1. extractionextracted 3 times with ethyl acetate
  2. dry with materialafter drying over MgSO4 and evaporation
  3. customthe crude product was purified by chromatograph) (silicagel, eluent: gradient of n-heptane/ethyl acetate)

출처 및 근거

ORD 기록
ord-7aac6d65b86b47ac843f7eada6c2ab1f
출처 데이터셋
uspto-grants-2005_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06890947B2

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