Methanol → HCID 19080750, compound

HRID 963162Notes

Reaction equation

HRID 963162 reaction equation
[CH2:1]([S:8][C:9]1[N:19]=[C:12]2[C:13]([Br:18])=[CH:14][CH:15]=[C:16](Cl)[N:11]2[N:10]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH3:20][O-:21].[Na+].CO>C(O)(=O)C>[CH2:1]([S:8][C:9]1[N:19]=[C:12]2[C:13]([Br:18])=[CH:14][CH:15]=[C:16]([O:21][CH3:20])[N:11]2[N:10]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Participants

5

Procedure

2-Benzylthio-8-bromo-5-chloro[1,2,4]triazolo[1,5-a]pyridine (7.7 g, 0.0217 mol) and 25 percent sodium methoxide in methanol (19.9 mL, 4.7 g, 0.0868 mol) were mixed with 400 mL of methanol and the mixture was heated to reflux for 1.5 hours. It was then cooled and acidified with acetic acid. The volatiles were removed by evaporation under reduced pressure and the residue was dissolved in dichloromethane The resulting solution was washed with water and concentrated by evaporation under reduced pressure. The resulting residue was triturated with hexane and the solids obtained were recovered by filtration and dried to obtain 7.3 g (96 percent of theory) of the title compound as a light tan powder melting at 78°-79° C.

Workup

  1. temperaturethe mixture was heated
  2. temperatureto reflux for 1.5 hours
  3. temperatureIt was then cooled
  4. customThe volatiles were removed by evaporation under reduced pressure
  5. dissolutionthe residue was dissolved in dichloromethane The resulting solution
  6. washwas washed with water
  7. concentrationconcentrated by evaporation under reduced pressure
  8. customThe resulting residue was triturated with hexane
  9. customthe solids obtained
  10. filtrationwere recovered by filtration
  11. customdried

Sources & evidence

ORD record
ord-34480b2128664ddeaac22e237a3f845a
Source dataset
uspto-grants-1998_06
Patent number
US05763359

Reaction notes

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