Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | Ahr 12245 | HCID 3082931 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 14390405 | HCID 14390405 | 52% |
Reaction Steps
A mixture of 2-(4-chlorophenyl)-3H-imidazo[4,5-b]pyridine-3-acetamide (1.84 g, 0.0064 mole), glacial acetic acid, and m-chloroperbenzoic acid (4.4 g, 0.0256 mole) was heated at 60° C. for a total of 4 hrs. The reaction mixture was diluted with water and the organic acid which precipitated was filtered. The aqueous filtrate was neutralized for peroxides with 10% sodium sulfite. The aqueous solution was evaporated to dryness and the residue was treated with methylene chloride/saturated sodium bicarbonate. The insoluble precipitate was filtered, washed with methylene chloride and water, and dried at 50° C. under high vacuum overnight to give 1.0 g (52%) of title compound, mp. 272°-75° C. with decomposition.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04948800 |
|---|
| Source dataset | uspto-grants-1990_08 |
|---|
| ORD ID | ord-7db11f6f6b3f42b6a3b827c84a83ab29 |
|---|
| Source note | uspto-grants-1990_08 |
|---|