Potassium peroxymonosulphate → HCID 58042463, compound

HRID 512072Notes

Reaction equation

HRID 512072 reaction equation
S([O-])(O[O-])(=O)=[O:2].[K+].[K+].[CH:9]([O:12][C:13]1[N:18]=[CH:17][C:16](B2OC(C)(C)C(C)(C)O2)=[CH:15][N:14]=1)([CH3:11])[CH3:10]>CC(C)=O.C(OCC)C>[CH:9]([O:12][C:13]1[N:18]=[CH:17][C:16]([OH:2])=[CH:15][N:14]=1)([CH3:11])[CH3:10]

Participants

5

Procedure

An aqueous solution (5 mL) of potassium peroxymonosulfate (1.40 g, 2.27 mmol) was added dropwise to a solution of 2-isopropoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrimidine (Preparation 100, 500 mg, 1.89 mmol) in acetone (5 ml) under a nitrogen atmosphere at 0° C. The mixture was stirred at room temperature for 2 hours, then filtered, the filtrate diluted with water (30 mL) and extracted with EtOAc (1×20 mL). The organic layer was washed with brine (2×20 mL), dried over sodium sulfate, filtered and evaporated in vacuo. The resulting oil was dissolved in dichloromethane and purified by silica gel chromatography eluting with 0 to 5% MeOH (with 10% aqueous ammonia) in dichloromethane to yield a solid. The solid was suspended in diethyl ether and evaporated to yield the title compound as a white solid (100 mg, 34%):

Workup

  1. filtrationfiltered
  2. additionthe filtrate diluted with water (30 mL)
  3. extractionextracted with EtOAc (1×20 mL)
  4. washThe organic layer was washed with brine (2×20 mL)
  5. dry with materialdried over sodium sulfate
  6. filtrationfiltered
  7. customevaporated in vacuo
  8. dissolutionThe resulting oil was dissolved in dichloromethane
  9. custompurified by silica gel chromatography
  10. washeluting with 0 to 5% MeOH (with 10% aqueous ammonia) in dichloromethane
  11. customto yield a solid
  12. customevaporated

Sources & evidence

ORD record
ord-5d89a5f649c04e5cb3c53989decb4c1a
Source dataset
uspto-grants-2015_08
Patent number
US09102621B2

Reaction notes

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