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Thiourea → 7-Nitroquinoline-4(1H)-thione

HRID 965004
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인쇄 미리보기

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HRID 965004 반응식
Cl[C:2]1[C:11]2[C:6](=[CH:7][C:8]([N+:12]([O-:14])=[O:13])=[CH:9][CH:10]=2)[N:5]=[CH:4][CH:3]=1.NC(N)=[S:17]>C(O)C>[N+:12]([C:8]1[CH:7]=[C:6]2[C:11]([C:2](=[S:17])[CH:3]=[CH:4][NH:5]2)=[CH:10][CH:9]=1)([O-:14])=[O:13]
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참가 물질

4

반응물 2

HCID 2723790ThioureaHCID 123225804-Chloro-7-nitroquinoline

생성물 1

HCID 190750667-Nitroquinoline-4(1H)-thione

시약·촉매·용매 1

HCID 702Ethanol용매

반응 조건

온도
80 °C

실험 절차

4-Chloro-7-nitroquinoline (100 mg, 0.48 mmol) and thiourea (100 mg, 1.3 mmol) were added to ethanol (50 ml) and stirred at 80° C. for 30 minutes. After allowing to cool to room temperature, ethanol was removed under reduced pressure. The residue was chromatographed by silica gel column chromatography and eluted with mixed solution of methylene chloride with methanol (19 : 1) for collection of yellow bands. The solvent was removed to obtain 7 mg (7%) of the titled yellow compound.

후처리

  1. temperatureto cool to room temperature
  2. customethanol was removed under reduced pressure
  3. customThe residue was chromatographed by silica gel column chromatography
  4. washeluted with mixed solution of methylene chloride with methanol (19 : 1) for collection of yellow bands
  5. customThe solvent was removed
  6. customto obtain 7 mg (7%) of the titled yellow compound

출처 및 근거

ORD 기록
ord-a6262e162148456bb565a1479526dd3f
출처 데이터셋
uspto-grants-1998_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05773449

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