Water → HCID 59334557, compound

HRID 1639793Notes

Reaction equation

HRID 1639793 reaction equation
[H-].[Na+].[I-].[CH3:4][S+](C)(C)=O.[Cl:9][C:10]1[CH:18]=[CH:17][C:16]2[C:12](=[CH:13][N:14]([CH3:19])[N:15]=2)[C:11]=1/[CH:20]=[CH:21]/[C:22]([O:24][CH2:25][CH3:26])=[O:23].O>CS(C)=O>[Cl:9][C:10]1[CH:18]=[CH:17][C:16]2[C:12](=[CH:13][N:14]([CH3:19])[N:15]=2)[C:11]=1[CH:20]1[CH2:4][CH:21]1[C:22]([O:24][CH2:25][CH3:26])=[O:23]

Participants

6

Procedure

To a suspension of sodium hydride (0.453 g, 10.4 mmol) in dimethyl sulfoxide (50.0 mL) was added a solution of trimethylsulfoxonium iodide (2.29 g, 10.4 mmol) in dimethyl sulfoxide (89 mL) at 0° C., and the mixture was stirred at room temperature for 1 hr. To the reaction mixture was added a solution of ethyl (2E)-3-(5-chloro-2-methyl-2H-indazol-4-yl)acrylate (4.20 g, 18.2 mmol) in dimethyl sulfoxide (50.0 mL) at 0° C., and the mixture was stirred at room temperature for 14 hr. Water was added, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by flash silica gel column chromatography (ethyl acetate/hexane=1/3) to give the title compound (2.10 g, yield 80%).

Workup

  1. stirringthe mixture was stirred at room temperature for 14 hr
  2. extractionthe mixture was extracted with ethyl acetate
  3. washThe extract was washed with saturated brine
  4. dry with materialdried over anhydrous sodium sulfate
  5. customthe solvent was evaporated under reduced pressure
  6. customThe residue was purified by flash silica gel column chromatography (ethyl acetate/hexane=1/3)

Sources & evidence

ORD record
ord-612360ae0e3f4e61b1a56848b77f784c
Source dataset
uspto-grants-2012_02
Patent number
US08110585B2

Reaction notes

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