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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Ammonia → Ammonia

HRID 1829176
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반응식

HRID 1829176 반응식
[NH3:1].[C:2]([N:5]1[CH2:10][CH2:9][CH2:8][CH2:7][C:6]1=O)(=[O:4])[CH3:3]>CO.[OH-].[Pd+2].[OH-]>[NH3:5].[C:2]([N:5]1[CH2:10][CH2:9][CH:8]([NH2:1])[CH2:7][CH2:6]1)(=[O:4])[CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 2

HCID 222AmmoniaHCID 118159051-Acetylpiperidin-2-one

생성물 2

HCID 222AmmoniaHCID 49624771-(4-Aminopiperidin-1-yl)ethan-1-one

시약·촉매·용매 2

HCID 9942167Palladium hydroxide촉매HCID 887Methanol용매

실험 절차

0.88 Ammonia (85 ml) was added to a solution of N-acetylpiperidone (15 g, 106 mmol) in methanol (120 ml), followed by palladium hydroxide (2 g) and the mixture hydrogenated at room temperature and 60 psi for 18 hours. The reaction mixture was filtered through Arbocel®, the filtrate concentrated under reduced pressure and the residue azeotroped with toluene to give a yellow oil. The crude product was purified by column chromatography on silica gel using an elution gradient of dichloromethane:methanol:0.88 ammonia (96:3.5:0.5 to 84:14:2) to afford the title compound as a clear oil, 9.6 g.

후처리

  1. filtrationThe reaction mixture was filtered through Arbocel®
  2. concentrationthe filtrate concentrated under reduced pressure
  3. customthe residue azeotroped with toluene
  4. customto give a yellow oil
  5. customThe crude product was purified by column chromatography on silica gel using an elution gradient of dichloromethane

출처 및 근거

ORD 기록
ord-3aeb0bdf566a4404b998247c8e514b62
출처 데이터셋
uspto-grants-2006_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07060836B2

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