HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Thiosulfate → 6-(2-Ethylsulfonylphenyl)-2-trifluoromethylimidazo[1,2-a]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 6-(2-Ethylsulfanylphenyl)-2-trifluoromethylimidazo[1,2-a]pyridine | HCID 72549031 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 6-(2-Ethylsulfonylphenyl)-2-trifluoromethylimidazo[1,2-a]pyridine | HCID 118205833 | — |
Reaction Steps
220 mg of 3-chloroperbenzoic acid (purity of 65% or more) was added to a mixture of 134 mg of 6-(2-ethylsulfanylphenyl)-2-trifluoromethylimidazo[1,2-a]pyridine and 4 ml of chloroform, under ice cooling, and the mixture was stirred at room temperature for 4 hours. A 10% aqueous sodium thiosulfate solution was added to the reaction mixture, and the mixture was extracted with chloroform. The organic layer was washed with a saturated aqueous sodium bicarbonate solution and dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. 93 mg of 6-(2-ethylsulfonylphenyl)-2-trifluoromethylimidazo[1,2-a]pyridine (Compound of Present invention 27) was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09328121B1 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-d3fbaa1deff74de4a37b6e599a6fe25c |
| Source note | uspto-grants-2016_05 |