Formic Acid → 7-Bromo-[1,2,4]triazolo[4,3-a]pyridine

HRID 1487896Notes

Reaction equation

HRID 1487896 reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][N:5]=[C:4]([NH:8][NH2:9])[CH:3]=1.[CH:10](O)=O>>[Br:1][C:2]1[CH:7]=[CH:6][N:5]2[CH:10]=[N:9][N:8]=[C:4]2[CH:3]=1

Participants

3

Conditions

Temperature
100 °C

Procedure

4-Bromo-2-hydrazinylpyridine (compound 41.1) was suspended in formic acid (3 mL). The mixture was heated at 100° C. for one hour, then upon complete reaction, the mixture cooled to room temperature. The volatile organics were removed under reduced pressure, then water (50 mL) was added to the residue. The solids that formed were filtered, washed with water and dried under reduced pressure at 50° C. to give 1.68 g (90%) of the title compound as an off-white solid. m/z (ES+) 198, 200 (M+H)+.

Workup

  1. customupon complete reaction
  2. temperaturethe mixture cooled to room temperature
  3. customThe volatile organics were removed under reduced pressure
  4. additionwater (50 mL) was added to the residue
  5. customThe solids that formed
  6. filtrationwere filtered
  7. washwashed with water
  8. customdried under reduced pressure at 50° C.

Sources & evidence

ORD record
ord-1368ebcab7934dd9aa7e60d567f1e4dd
Source dataset
uspto-grants-2016_08
Patent number
US09428502B2

Reaction notes

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