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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Ethanol → 1-(2-Aminopyridin-4-yl)ethanol

HRID 1845866
노트
인쇄 미리보기

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HRID 1845866 반응식
N([C:3]1[N:8]=[C:7]([CH:9]([OH:11])[CH3:10])[CH:6]=[CH:5][N:4]=1)N.[CH2:12](O)C>CO.[Ni]>[NH2:8][C:3]1[CH:12]=[C:7]([CH:9]([OH:11])[CH3:10])[CH:6]=[CH:5][N:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 702EthanolHCID 672565471-(2-Hydrazinopyrimidin-4-yl)ethanol

생성물 1

HCID 179991481-(2-Aminopyridin-4-yl)ethanol

시약·촉매·용매 2

HCID 935Nickel촉매HCID 887Methanol용매

실험 절차

1-(2-hydrazinopyrimidin-4-yl)ethanol (13a) was dissolved in ethanol (300 mL) and Raney-Ni (35 mL, 50% slurry in water) was added. The flask was flushed with argon, put under a hydrogen atmosphere (balloon) and stirred at room temperature overnight. The mixture was filtered and concentrated under vacuum to give a red oil that was dissolved in methanol and concentrated onto silica before being purified by silica flash chromatography (100% ethyl acetate to 20% methanol in ethyl acetate) to give the title compound (9.0 g) as an orange oil.

후처리

  1. customThe flask was flushed with argon
  2. filtrationThe mixture was filtered
  3. concentrationconcentrated under vacuum
  4. customto give a red oil that
  5. concentrationconcentrated onto silica
  6. custombefore being purified by silica flash chromatography (100% ethyl acetate to 20% methanol in ethyl acetate)

출처 및 근거

ORD 기록
ord-e95419049608414fa222b2aac96e5390
출처 데이터셋
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08952001B2

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