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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2272903Generated: October 31, 2026

Sodium Thiosulfate → HCID 117974288, compound

https://huagongshe.com/reaction/2272903

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 117974266HCID 117974266—
SolventChloroformHCID 6212—
ProductHCID 117974288HCID 117974288—
ProductHCID 117974434HCID 117974434—

Reaction Steps

0.25 g of 3-chloroperoxybenzoic acid (69 to 75%) was added to a mixture of 0.25 g of 2-(3-ethylthiothiophen-2-yl)-3-methyl-6-trifluoromethyl-3H-imidazo[4,5-b]pyridine and 5 ml of chloroform, under ice cooling, then the mixture was heated to room temperature and stirred for 1 hour. A saturated aqueous sodium bicarbonate solution and a saturated aqueous sodium thiosulfate solution were poured to the reaction mixture, and the mixture was extracted twice with ethyl acetate. The combined organic layers were dried over anhydrous sodium sulfate and then concentrated under reduced pressure. The resulting residue was applied to a silica gel column chromatography to obtain 0.10 g of 2-(3-ethylsulfinylthiophen-2-yl)-3-methyl-6-trifluoromethyl-3H-imidazo[4,5-b]pyridine (Compound of Present Invention (16)) and 0.12 g of 2-(3-ethylsulfonylthiophen-2-yl)-3-methyl-6-trifluoromethyl-3H-imidazo[4,5-b]pyridine (Compound of Present Invention (17)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120792B2
Source datasetuspto-grants-2015_09
ORD IDord-b39dc9f5c8f543cfb9b024a008d5bb3a
Source noteuspto-grants-2015_09