HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 713670Generated: October 29, 2026
Dabco → 3-ethylsulfanyl-N-(5-trifluoromethylsulfanylpyridin-2-yl)picolinamide
https://huagongshe.com/reaction/713670
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dabco | HCID 9237 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 2-Chloro-5-((trifluoromethyl)sulfanyl)pyridine | HCID 75406410 | — |
| Reactant | 3-Ethylsulfanylpicolinic acid amide | HCID 118113333 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-ethylsulfanyl-N-(5-trifluoromethylsulfanylpyridin-2-yl)picolinamide | HCID 118205931 | 37.6% |
Reaction Steps
A mixture of 0.64 g of 2-chloro-5-trifluoromethylsulfanylpyridine, 0.54 g of 3-ethylsulfanylpicolinic acid amide, 1.96 g of cesium carbonate, 0.33 g of DABCO and 5 mL of DMSO was stirred at 70° C. for 1 hour. Water was added to the reaction mixture cooled to room temperature, and the mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate and then concentrated under reduced pressure, and the resulting residue was applied to a silica gel column chromatography to obtain 0.40 g of 3-ethylsulfanyl-N-(5-trifluoromethylsulfanylpyridin-2-yl)picolinamide (hereinafter, referred to as Compound of Present Invention 48).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09185910B2 |
|---|
| Source dataset | uspto-grants-2015_11 |
|---|
| ORD ID | ord-0335cbff07a24aa480734073312bb7fe |
|---|
| Source note | uspto-grants-2015_11 |
|---|