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HCID 21108202, 화합물 → HCID 21108382, 화합물

HRID 1766007
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HRID 1766007 반응식
C([N:4]1[C:12]2[C:7](=[CH:8][C:9]([CH:13](O)[CH2:14][CH2:15][N:16]([CH3:18])[CH3:17])=[CH:10][CH:11]=2)[CH2:6][CH2:5]1)(=O)C>Cl>[NH:4]1[C:12]2[C:7](=[CH:8][C:9](/[CH:13]=[CH:14]/[CH2:15][N:16]([CH3:18])[CH3:17])=[CH:10][CH:11]=2)[CH2:6][CH2:5]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 21108202HCID 21108202, 화합물

생성물 1

HCID 21108382HCID 21108382, 화합물

시약·촉매·용매 1

HCID 313Hydrochloric Acid용매

실험 절차

A mixture of 3-[1-acetyl-2,3-dihydro-1H-indol-5-yl]-3-hydroxy-N,N-dimethyl-1-propanamine (3.3 g) obtained in 1) above and concd. hydrochloric acid (20 ml) was heated for 16 hours under reflux. The reaction solution was cooled to room temperature, then concentrated under reduced pressure, diluted with water, made basic with 2 N aqueous sodium hydroxide and extracted with ethyl acetate. The extract was washed with a saturated saline solution and dried over anhydrous magnesium sulfate, and the solvent was distilled away under reduced pressure, whereby the title compound (2.3 g) was obtained as oily matter.

후처리

  1. customobtained in 1) above and concd
  2. temperatureunder reflux
  3. concentration
concentrated under reduced pressure
  • additiondiluted with water
  • extractionextracted with ethyl acetate
  • washThe extract was washed with a saturated saline solution
  • dry with materialdried over anhydrous magnesium sulfate
  • distillationthe solvent was distilled away under reduced pressure, whereby the title compound (2.3 g)
  • customwas obtained as oily matter
  • 출처 및 근거

    ORD 기록
    ord-30a2e3291e6c4eb49aec0fc8f1afc66a
    출처 데이터셋
    uspto-grants-2007_06
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US07229986B2

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