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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Methylmercaptan sodium | HCID 45051789 | — |
| Reactant | 2-(3-Fluoropyridin-4-yl)-6-(trifluoromethyl)thiazolo[5,4-b]pyridine | HCID 68153707 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-[3-(Methylthio)pyridin-4-yl]-6-(trifluoromethyl)thiazolo[5,4-b]pyridine | HCID 68153884 | 87.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08742112B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-f25230b68e4f4c68af4bfd992b07ac32 |
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| Source note | uspto-grants-2014_06 |
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