HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 2-[3-(Methylthio)pyridin-4-yl]-5-(trifluoromethyl)benzothiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Methylmercaptan sodium | HCID 45051789 | — |
| Reactant | 2-(3-Fluoropyridin-4-yl)-5-(trifluoromethyl)benzothiazole | HCID 67113761 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-[3-(Methylthio)pyridin-4-yl]-5-(trifluoromethyl)benzothiazole | HCID 67113933 | — |
Reaction Steps
A mixture of 0.30 g of 2-(3-fluoropyridin-4-yl)-5-(trifluoromethyl)benzothiazole, 0.14 g of methylmercaptan sodium salt and 3 ml of DMF was stirred at room temperature for 20 minutes. To the reaction mixture was added water, and the resultant mixture was extracted with ethyl acetate three times. 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 2-[3-(methylthio)pyridin-4-yl]-5-(trifluoromethyl)benzothiazole (hereinafter, referred to as the present compound 5).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08742112B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-f51d624970024d0eb930e131fc92d8bc |
| Source note | uspto-grants-2014_06 |