Water → HCID 66720614, compound

HRID 1639807Notes

Reaction equation

HRID 1639807 reaction equation
[H-].[Na+].C(OP([CH2:11][C:12]([O:14][CH2:15][CH3:16])=[O:13])(OCC)=O)C.[F:17][C:18]1[C:26]2[C:22](=[CH:23][N:24]([CH3:27])[N:25]=2)[C:21]([CH:28]=O)=[CH:20][CH:19]=1.O>O1CCCC1>[F:17][C:18]1[C:26]2[C:22](=[CH:23][N:24]([CH3:27])[N:25]=2)[C:21](/[CH:28]=[CH:11]/[C:12]([O:14][CH2:15][CH3:16])=[O:13])=[CH:20][CH:19]=1

Participants

6

Reactant 4

HCID 962WaterHCID 13345Triethyl phosphonoacetateHCID 24758Sodium hydrideHCID 59334530HCID 59334530, compound

Product 1

HCID 66720614HCID 66720614, compoundYield 83%

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent3×

Procedure

To a suspension of sodium hydride (0.467 g, 11.7 mmol) in tetrahydrofuran (10 mL) was added a solution of ethyl diethylphosphonoacetate (2.34 mL, 11.7 mmol) in tetrahydrofuran (3 mL) at 0° C., and the mixture was stirred for 20 min. To the reaction mixture was added a solution of 7-fluoro-2-methyl-2H-indazole-4-carbaldehyde (1.60 g, 8.98 mmol) in tetrahydrofuran (5 mL), and the mixture was warmed to room temperature over 4 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 is was purified by silica gel column chromatography (ethyl acetate/hexane=1/3) to give the title compound (1.85 g, yield 83%).

Workup

  1. extractionthe mixture was extracted with ethyl acetate
  2. washThe extract was washed with saturated brine
  3. dry with materialdried over anhydrous sodium sulfate
  4. customthe solvent was evaporated under reduced pressure
  5. customThe residue is was purified by silica gel column chromatography (ethyl acetate/hexane=1/3)

Sources & evidence

ORD record
ord-7c93a39e01f64c9cbda137eb8135f20e
Source dataset
uspto-grants-2012_02
Patent number
US08110585B2

Reaction notes

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