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2-chloro-N-(3-(dibenzylamino)-2-hydroxypropyl)acetamide → 6-((Dibenzylamino)methyl)morpholin-3-one

HRID 57598
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인쇄 미리보기

반응식

HRID 57598 반응식
Cl[CH2:2][C:3]([NH:5][CH2:6][CH:7]([OH:24])[CH2:8][N:9]([CH2:17][C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)[CH2:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)=[O:4].CC([O-])(C)C.[K+]>CC(O)(C)C>[CH2:10]([N:9]([CH2:8][CH:7]1[CH2:6][NH:5][C:3](=[O:4])[CH2:2][O:24]1)[CH2:17][C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 117252152-chloro-N-(3-(dibenzylamino)-2-hydroxypropyl)acetamideHCID 23665647Potassium tert-butoxide

생성물 1

HCID 99955506-((Dibenzylamino)methyl)morpholin-3-one

시약·촉매·용매 1

HCID 6386tert-Butanol용매

실험 절차

A solution of 2-chloro-N-(3-(dibenzylamino)-2-hydroxypropyl)acetamide (1.0 g, 2.49 mmol), t-BuOK (0.39 g, 3.57 mmol) in t-BuOH (30 mL) was stirred at reflux overnight. After concentration, the residue was purified by column chromatography to give product as white solid.

후처리

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
temperature
at reflux overnight
  • concentrationAfter concentration
  • customthe residue was purified by column chromatography
  • customto give product as white solid
  • 출처 및 근거

    ORD 기록
    ord-3554ed25db0f4d5a8f454c2d718e4f90
    출처 데이터셋
    uspto-grants-2016_09
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US09434726B2

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