Ethanol → HCID 21984597, compound

HRID 2253376Notes

Reaction equation

HRID 2253376 reaction equation
[Br:1][C:2]1[N:7]2[N:8]=[C:9]([O:11][CH3:12])[CH:10]=[C:6]2[CH:5]=[CH:4][CH:3]=1.[N:13]([O-])=O.[Na+].C(O)C.O>C(O)(=O)C.[Zn]>[Br:1][C:2]1[N:7]2[N:8]=[C:9]([O:11][CH3:12])[C:10]([NH2:13])=[C:6]2[CH:5]=[CH:4][CH:3]=1

Participants

7

Procedure

To a solution of 7-bromo-2-methoxypyrazolo[1,5-a]pyridine (1 g) dissolved in acetic acid (10 mL) was added an aqueous solution (5 mL) of sodium nitrite (334 mg), and the reaction mixture was stirred for 20 minutes at room temperature. After adding ethanol (60 mL) and water (30 mL) to the reaction mixture, zinc powder (1 g) was added and the reaction mixture was heated and stirred for 30 minutes at 60° C. The reaction mixture was filtered through celite to remove insoluble residue, water was added and extraction was performed with ethyl acetate. The organic extract was washed with brine, dried over anhydrous magnesium sulfate and filtered, the solvent was evaporated under reduced pressure, the residue was purified by silica gel column chromatography and the title compound (750 mg) was obtained as brown crystals from the n-hexane:ethyl acetate (3:1) fraction.

Workup

  1. additionwas added
  2. temperaturethe reaction mixture was heated
  3. stirringstirred for 30 minutes at 60° C
  4. filtrationThe reaction mixture was filtered through celite
  5. customto remove insoluble residue, water
  6. additionwas added
  7. extractionextraction
  8. extractionThe organic extract
  9. washwas washed with brine
  10. dry with materialdried over anhydrous magnesium sulfate
  11. filtrationfiltered
  12. customthe solvent was evaporated under reduced pressure
  13. customthe residue was purified by silica gel column chromatography

Sources & evidence

ORD record
ord-1ac12f0997b54b5490aabcf710547719
Source dataset
uspto-grants-2008_01
Patent number
US07323569B2

Reaction notes

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