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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 402336Generated: October 30, 2026

Dimethylformamide → 2-[3-(Methylthio)pyridin-4-yl]-6-(trifluoromethyl)thiazolo[5,4-b]pyridine

https://huagongshe.com/reaction/402336

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantMethylmercaptan sodiumHCID 45051789—
Reactant2-(3-Fluoropyridin-4-yl)-6-(trifluoromethyl)thiazolo[5,4-b]pyridineHCID 68153707—
SolventWaterHCID 962—
Product2-[3-(Methylthio)pyridin-4-yl]-6-(trifluoromethyl)thiazolo[5,4-b]pyridineHCID 6815388487.8%

Reaction Steps

A mixture of 0.20 g of 2-(3-fluoropyridin-4-yl)-6-(trifluoromethyl)thiazolo[5,4-b]pyridine, 47 mg of methylmercaptan sodium salt and 6 ml of DMF was stirred for 1 hour under ice cool. To this mixture was added 47 mg of methylmercaptan sodium salt, and the resultant mixture was stirred further for 1 hour under ice cool. To the reaction mixture was added water, and the resultant mixture was extracted with ethyl acetate twice. The combined organic layers were washed with water and saturated saline, dried over magnesium sulfate, then, concentrated under reduced pressure. The residue was subjected to silica gel column chromatography, to obtain 0.19 g of 2-[3-(methylthio)pyridin-4-yl]-6-(trifluoromethyl)thiazolo[5,4-b]pyridine (hereinafter, referred to as the present compound 14).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08742112B2
Source datasetuspto-grants-2014_06
ORD IDord-f25230b68e4f4c68af4bfd992b07ac32
Source noteuspto-grants-2014_06