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Ethanol → 9-ethyl-7,9-dihydro-2-phenyl-8H-purin-8-one

HRID 842075
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인쇄 미리보기

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HRID 842075 반응식
[CH2:1]([NH:3][C:4]1[C:9]([N+:10]([O-])=O)=[CH:8][N:7]=[C:6]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[N:5]=1)[CH3:2].[CH2:19]([OH:21])C>[C].[Pd]>[CH2:1]([N:3]1[C:19](=[O:21])[NH:10][C:9]2[C:4]1=[N:5][C:6]([C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)=[N:7][CH:8]=2)[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 702EthanolHCID 226177974-Ethylamino-5-nitro-2-phenylpyrimidine

생성물 1

HCID 226177959-ethyl-7,9-dihydro-2-phenyl-8H-purin-8-one

시약·촉매·용매 1

HCID 178418390HCID 178418390, 화합물촉매

실험 절차

A mixture of 4-ethylamino-5-nitro-2-phenylpyrimidine (2.7 g), palladium-carbon (0.3 g), and ethanol (50 ml) is stirred at room temperature under hydrogen atmosphere for five hours, and the reaction mixture is filtered. The filtrate is concentrated under reduced pressure, and to the resulting residue is added urea (1.4 g). The mixture is stirred at 200° C. for two hours. After cooling, water is added to the reaction mixture, and the precipitates are collected by filtration, washed with water, and washed with ethanol to give the desired compound (2.4 g).

후처리

  1. filtrationthe reaction mixture is filtered
  2. concentrationThe filtrate is concentrated under reduced pressure
  3. additionto the resulting residue is added urea (1.4 g)
  4. stirringThe mixture is stirred at 200° C. for two hours
  5. temperatureAfter cooling
  6. additionwater is added to the reaction mixture
  7. filtrationthe precipitates are collected by filtration
  8. washwashed with water
  9. washwashed with ethanol

출처 및 근거

ORD 기록
ord-58e0c421d4eb495fa94b7bc315b76d8c
출처 데이터셋
uspto-grants-2002_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06372740B1

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