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Methanesulfonyl chloride → N-[2-(1H-Indol-5-yl)ethyl]methanesulphonamide

HRID 1087409
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반응식

HRID 1087409 반응식
[NH:1]1[C:9]2[C:4](=[CH:5][C:6]([CH2:10][CH2:11][NH2:12])=[CH:7][CH:8]=2)[CH:3]=[CH:2]1.[CH3:13][S:14](Cl)(=[O:16])=[O:15].C(=O)(O)[O-].[Na+]>C(OCC)(=O)C>[NH:1]1[C:9]2[C:4](=[CH:5][C:6]([CH2:10][CH2:11][NH:12][S:14]([CH3:13])(=[O:16])=[O:15])=[CH:7][CH:8]=2)[CH:3]=[CH:2]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 31297Methanesulfonyl chlorideHCID 516892Sodium BicarbonateHCID 172211022-(1H-Indol-5-yl)ethan-1-amine

생성물 1

HCID 19817119N-[2-(1H-Indol-5-yl)ethyl]methanesulphonamide

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매

실험 절차

A mixture of 1H-indole-5-ethanamine (1.00 g), methane sulphonylchloride (0.69 ml), 8% sodium bicarbonate solution (100 ml) and ethyl acetate (100 ml) were stirred vigorously for 20 min. The organic phase was separated and the aqueous phase extracted with ethyl acetate (50 ml). The combined organic phases were dried and evaporated in vacuo to give the title compound as an oil (1.50 g). T.l.c. SiO2, EtOAc Rf 0.8

후처리

  1. customThe organic phase was separated
  2. extractionthe aqueous phase extracted with ethyl acetate (50 ml)
  3. customThe combined organic phases were dried
  4. customevaporated in vacuo

출처 및 근거

ORD 기록
ord-b0c49db82bb143bcbbd10bab183ebc9e
출처 데이터셋
uspto-grants-1991_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05036078

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