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Isopropanol → 6-(3-Trifluoromethyl-benzenesulfonyl)-2H-pyridazin-3-one

HRID 1581483
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HRID 1581483 반응식
Cl[C:2]1[N:3]=[N:4][C:5](Cl)=[CH:6][CH:7]=1.[Na+].[F:10][C:11]([F:22])([F:21])[C:12]1[CH:13]=[C:14]([S:18]([O-:20])=[O:19])[CH:15]=[CH:16][CH:17]=1.C([OH:26])(C)C>O>[F:22][C:11]([F:10])([F:21])[C:12]1[CH:13]=[C:14]([S:18]([C:2]2[CH:7]=[CH:6][C:5](=[O:26])[NH:4][N:3]=2)(=[O:20])=[O:19])[CH:15]=[CH:16][CH:17]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 3776IsopropanolHCID 673313,6-DichloropyridazineHCID 23677070Sodium 3-(trifluoromethyl)benzene-1-sulfinate

생성물 1

HCID 98149486-(3-Trifluoromethyl-benzenesulfonyl)-2H-pyridazin-3-one수율 25%

시약·촉매·용매 1

HCID 962Water용매2회

실험 절차

A mixture of 3,6-dichloropyridazine (4.44 g), 3-trifluoromethylphenyl sulfinic acid sodium salt (6.93 g), isopropanol (30 mL), and water (1 mL) was prepared and refluxed for 18 hours. The reaction mixture was then cooled, diluted with water (100 mL) and the precipitated solid was collected. The solid was triturated with n-propanol and the solid was collected to obtain the title compound (25%, 2.3 g).

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후처리

  1. customwas prepared
  2. temperaturerefluxed for 18 hours
  3. temperatureThe reaction mixture was then cooled
  4. customthe precipitated solid was collected
  5. customThe solid was triturated with n-propanol
  6. customthe solid was collected

출처 및 근거

ORD 기록
ord-fc9bcf3322d74756910a49132f064806
출처 데이터셋
uspto-grants-2004_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06730674B2

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