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2-Methoxyethylamine → HCID 54038932, 화합물

HRID 264937
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HRID 264937 반응식
CO[C:3](=[O:18])[CH2:4][CH2:5][CH2:6][NH:7][C:8]([O:10][CH2:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)=[O:9].[CH3:19][O:20][CH2:21][CH2:22][NH2:23]>C(O)C>[CH3:19][O:20][CH2:21][CH2:22][NH:23][C:3](=[O:18])[CH2:4][CH2:5][CH2:6][NH:7][C:8]([O:10][CH2:11][C:12]1[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=1)=[O:9]
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참가 물질

4

반응물 2

HCID 80182-MethoxyethylamineHCID 13874704Methyl 4-{[(benzyloxy)carbonyl]amino}butanoate

생성물 1

HCID 54038932HCID 54038932, 화합물

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

5.02 g of 4-benzyloxycarbonylaminobutyric acid methyl ester are stirred under reflux in 35 ml of ethanol with 15 ml of 2-methoxyethylamine for 5 days. The reaction mixture is concentrated by evaporation and the residue is purified by means of FC (240 g of silica gel, dichloromethane/methanol=95:5). The title compound is obtained: Rf (dichloromethane/methanol=95:5)=0.33.

후처리

  1. concentrationThe reaction mixture is concentrated by evaporation
  2. customthe residue is purified by means of FC (240 g of silica gel, dichloromethane/methanol=95:5)

출처 및 근거

ORD 기록
ord-7cce6d6c23a84d6bada430e2885e0194
출처 데이터셋
uspto-grants-1997_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05646143

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