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Triethyl phosphite → diethyl[(6S*,9aR*)-6-(2-fluorophenyl)-4-oxooctahydroquinolizin-3-yl]phosphonate

HRID 553913
노트
인쇄 미리보기

반응식

HRID 553913 반응식
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C@H:8]1[CH2:17][CH2:16][CH2:15][C@@H:14]2[N:9]1[C:10](=[O:19])[CH:11](I)[CH2:12][CH2:13]2.[P:20]([O:27]CC)([O:24][CH2:25][CH3:26])[O:21][CH2:22][CH3:23]>>[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C@@H:8]1[CH2:17][CH2:16][CH2:15][C@H:14]2[N:9]1[C:10](=[O:19])[CH:11]([P:20](=[O:27])([O:24][CH2:25][CH3:26])[O:21][CH2:22][CH3:23])[CH2:12][CH2:13]2
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 31215Triethyl phosphiteHCID 69069771(6R*,9aS*)-6-(2-fluorophenyl)-3-iodooctahydroquinolizin-4-one

생성물 1

HCID 86612702diethyl[(6S*,9aR*)-6-(2-fluorophenyl)-4-oxooctahydroquinolizin-3-yl]phosphonate

반응 조건

온도
120 °C

실험 절차

A mixture of (6R*,9aS*)-6-(2-fluorophenyl)-3-iodooctahydroquinolizin-4-one (500 mg) with triethyl phosphite (6 mL) was stirred at 120° C. for five hours. The reaction solution was left to cool to room temperature and then concentrated under reduced pressure to obtain 501 mg of the title compound. The property value of the compound is as follows.

후처리

  1. wait
The reaction solution was left
  • temperatureto cool to room temperature
  • concentrationconcentrated under reduced pressure
  • 출처 및 근거

    ORD 기록
    ord-894ad5e2aa42465294e6b06c69f07c95
    출처 데이터셋
    uspto-grants-2011_11
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US08048878B2

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