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5-(((2-Aminoethyl)thio)methyl)-N,N-dimethyl-2-furanmethanamine → 2-[2-(5-Dimethylaminomethyl-2-furylmethylthio)ethylamino]-3-nitropyrrole

HRID 1065770
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반응식

HRID 1065770 반응식
[CH3:1][N:2]([CH2:4][C:5]1[O:9][C:8]([CH2:10][S:11][CH2:12][CH2:13][NH2:14])=[CH:7][CH:6]=1)[CH3:3].CS([C:18]1[NH:19][CH:20]=[CH:21][C:22]=1[N+:23]([O-:25])=[O:24])=O>C(O)C>[CH3:3][N:2]([CH2:4][C:5]1[O:9][C:8]([CH2:10][S:11][CH2:12][CH2:13][NH:14][C:18]2[NH:19][CH:20]=[CH:21][C:22]=2[N+:23]([O-:25])=[O:24])=[CH:7][CH:6]=1)[CH3:1]
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참가 물질

4

반응물 2

HCID 1622035-(((2-Aminoethyl)thio)methyl)-N,N-dimethyl-2-furanmethanamineHCID 130595162-Methylsulphinyl-3-nitropyrrole

생성물 1

HCID 136466382-[2-(5-Dimethylaminomethyl-2-furylmethylthio)ethylamino]-3-nitropyrrole

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A solution of 2-(5-dimethylaminomethyl-2-furylmethylthio)ethylamine (3 g, 0.014 mol) and 2-methylsulphinyl-3-nitropyrrole (2 g, 0.011 mol) in ethanol (50 ml) was refluxed for 7 days, and it was then evaporated to dryness. The residue was purified by elution from a column of silica gel with ethyl acetate-petroleum ether (b.p. 60°-80°)(4:1) to give 2-[2-(5-dimethylaminomethyl-2-furylmethylthio)ethylamino]-3-nitropyrrole, m.p. 67°-67°.

후처리

  1. customit was then evaporated to dryness
  2. customThe residue was purified by elution from a column of silica gel with ethyl acetate-petroleum ether (b.p. 60°-80°)(4:1)

출처 및 근거

ORD 기록
ord-c46d9b8fa97746938994dcec7abe1ea2
출처 데이터셋
uspto-grants-1982_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04331668

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