HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2201351Generated: October 29, 2026
Sodium Thiosulfate → HCID 117988775, compound
https://huagongshe.com/reaction/2201351
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 117988884 | HCID 117988884 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 117988775 | HCID 117988775 | — |
Reaction Steps
542 mg of 3-chloroperoxybenzoic acid (purity of 65% or more) was added to a mixture of 416 mg of 2-(2-ethylsulfanyl-6-trifluoromethylpyridin-3-yl)-3-methyl-6-trifluoromethyl-3H-imidazo[4,5-b]pyridine and 5 ml of chloroform, and the mixture was stirred at room temperature for 1 hour, then allowed to stand at room temperature overnight. A 10% aqueous sodium thiosulfate solution was poured 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, then concentrated under reduced pressure to obtain 452 mg of 2-(2-ethylsulfonyl-6-trifluoromethylpyridin-3-yl)-3-methyl-6-trifluoromethyl-3H-imidazo[4,5-b]pyridine (hereinafter, referred to as Compound of Present Invention 5).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09364000B2 |
|---|
| Source dataset | uspto-grants-2016_06 |
|---|
| ORD ID | ord-52f7deaa47e9444ea88dbbedce080a03 |
|---|
| Source note | uspto-grants-2016_06 |
|---|