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2-(6-Azidopyrimidin-4-yloxy)ethanol → 2-((6-Aminopyrimidin-4-yl)oxy)ethanol

HRID 2313
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인쇄 미리보기

반응식

HRID 2313 반응식
[N:1]([C:4]1[N:9]=[CH:8][N:7]=[C:6]([O:10][CH2:11][CH2:12][OH:13])[CH:5]=1)=[N+]=[N-]>[C].[Pd].C(O)C>[NH2:1][C:4]1[N:9]=[CH:8][N:7]=[C:6]([O:10][CH2:11][CH2:12][OH:13])[CH:5]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 189310712-(6-Azidopyrimidin-4-yloxy)ethanol

생성물 1

HCID 189310692-((6-Aminopyrimidin-4-yl)oxy)ethanol수율 79%

시약·촉매·용매 2

HCID 178418390HCID 178418390, 화합물촉매HCID 702Ethanol용매

실험 절차

A mixture of 2-(6-azidopyrimidin-4-yloxy)ethanol (1.64 g), 10% palladium-carbon (0.25 g) and ethanol (20 ml) is subjected to catalytic hydrogenation at room temperature for one hour under hydrogen atmosphere (1 atm). The catalyst is removed by filtration, and the filtrate is concentrated. The residue is recrystallized from ethanol/diethyl ether to give 2-(6-aminopyrimidin-4-yloxy)ethanol (1.11 g).

후처리

  1. customThe catalyst is removed by filtration
  2. concentrationthe filtrate is concentrated
  3. customThe residue is recrystallized from ethanol/diethyl ether

출처 및 근거

ORD 기록
ord-fa1f51d360144913905861053111ec80
출처 데이터셋
uspto-grants-1998_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05728706

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