Hydrogen Peroxide → HCID 18412598, compound

HRID 992596Notes

Reaction equation

HRID 992596 reaction equation
[CH3:1][N:2]1[C:10]2[C:5](=[N:6][C:7]([CH:11]=[O:12])=[CH:8][CH:9]=2)[N:4]=[C:3]1[CH2:13][O:14][C:15]1[CH:20]=[CH:19][C:18]([C:21]#[N:22])=[CH:17][CH:16]=1.[OH:23]O>C(O)=O>[CH3:1][N:2]1[C:10]2[C:5](=[N:6][C:7]([C:11]([OH:23])=[O:12])=[CH:8][CH:9]=2)[N:4]=[C:3]1[CH2:13][O:14][C:15]1[CH:20]=[CH:19][C:18]([C:21]#[N:22])=[CH:17][CH:16]=1

Participants

4

Procedure

1.25 g (4.3 mMol) of 1-methyl-2-[(4-cyanophenyl)oxymethyl]-imidazo[4,5-b]pyridine-5-carbaldehyde were dissolved in 10 ml formic acid and mixed at 0° C. with 1.0 ml hydrogen peroxide (33% strength). After 12 hours at 40° C. the white precipitate formed was suction filtered, washed with water and dried at 40° C.

Workup

  1. customAfter 12 hours at 40° C. the white precipitate formed
  2. filtrationfiltered
  3. washwashed with water
  4. customdried at 40° C.

Sources & evidence

ORD record
ord-4543be517f10459db31e334a2888aca7
Source dataset
uspto-grants-2002_10
Patent number
US06469039B1

Reaction notes

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