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

HRID 985394
Notes
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Reaction equation

HRID 985394 reaction equation
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
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

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

Product 1

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

Reagents, catalysts & solvents 1

HCID 962WaterSolvent2×

Procedure

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).

Workup

  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

Sources & evidence

ORD record
ord-2649920c980845a2903bc87f12431de7
Source dataset
uspto-grants-2005_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06872722B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes