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Chloroform → N-[2-hydroxy-3-(1-piperidinyl)propoxy]-N'-heptyl-urea

HRID 19749
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인쇄 미리보기

반응식

HRID 19749 반응식
[NH2:1][O:2][CH2:3][CH:4]([OH:12])[CH2:5][N:6]1[CH2:11][CH2:10][CH2:9][CH2:8][CH2:7]1.C(Cl)(Cl)Cl.[CH2:17]([N:24]=[C:25]=[O:26])[CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH3:23]>>[OH:12][CH:4]([CH2:5][N:6]1[CH2:11][CH2:10][CH2:9][CH2:8][CH2:7]1)[CH2:3][O:2][NH:1][C:25]([NH:24][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH3:23])=[O:26]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 6212ChloroformHCID 138341n-Heptyl isocyanateHCID 187662101-(Aminooxy)-3-(piperidin-1-yl)propan-2-ol

생성물 1

HCID 18766188N-[2-hydroxy-3-(1-piperidinyl)propoxy]-N'-heptyl-urea

실험 절차

To the solution of 1.23 g (7.1 mmol) of l-aminooxy-2-hydroxy-3-(1-piperidinyl)-propane dissolved in 20 ml of chloroform 1.0 g (7.1 mmol) of heptyl isocyanate was added and the reaction mixture was stirred for 20 hours. Solvent was evaporated in vacuum and the residue was purified by chromatography to give pure colorless oil. White crystalline product was obtained by triturating with petroleum ether.

후처리

  1. additionwas added
custom
Solvent was evaporated in vacuum
  • customthe residue was purified by chromatography
  • customto give pure colorless oil
  • customWhite crystalline product was obtained
  • customby triturating with petroleum ether
  • 출처 및 근거

    ORD 기록
    ord-5d41a87368eb46de9294345e9b841d10
    출처 데이터셋
    uspto-grants-2010_06
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US07745465B2

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