HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2272897Generated: October 30, 2026
Sodium Thiosulfate → HCID 117974529, compound
https://huagongshe.com/reaction/2272897
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 72203603 | HCID 72203603 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 117974529 | HCID 117974529 | — |
Reaction Steps
0.08 g of 3-chloroperoxybenzoic acid (purity of 65% or more) was added to a solution of 0.06 g of 2-(3-ethylthio-5-trifluoromethylthiophen-2-yl)-3-methyl-6-t rifluoromethyl-3H-imidazo[4,5,b]pyridine in 3 ml of chloroform under ice cooling, and the mixture was stirred for 2 hours and at room temperature for 1 hour. A 10% aqueous sodium thiosulfate solution was poured into the reaction mixture, and the mixture was extracted with chloroform. The organic layer was washed with a saturated aqueous sodium bicarbonate solution, then dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The resulting residue was applied to a silica gel column chromatography to obtain 0.06 g of 2-(3-ethylsulfonyl-5-trifluoromethylthiophen-2-yl)-3-methyl-6-trifluoromethyl-3H-imidazo[4,5,b]pyridine (Compound of Present Invention (6)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09120792B2 |
|---|
| Source dataset | uspto-grants-2015_09 |
|---|
| ORD ID | ord-486c7fa54d08420caf22519799861b68 |
|---|
| Source note | uspto-grants-2015_09 |
|---|