HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 660059Erstellt: 26. Oktober 2026
Potassium Carbonate → 2-[2-(4-fluorophenyl)sulfonylethylthio]-N-(2-thienylmethyl)-nicotinamide
https://huagongshe.com/reaction/660059
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 1-(2-Chloroethanesulfonyl)-4-fluorobenzene | HCID 2736505 | — |
| Edukt | Dichloromethane ethylacetate | HCID 21226138 | — |
| Edukt | 2-mercapto-N-(thiophen-2-ylmethyl)nicotinamide | HCID 178523048 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 2-[2-(4-fluorophenyl)sulfonylethylthio]-N-(2-thienylmethyl)-nicotinamide | HCID 68726873 | 48% |
Reaktionsschritte
303 mg (2.2 mmol) of K2CO3 were added to a solution of 500 mg (2.0 mmol) of 2-mercapto-N-(thiophen-2-ylmethyl)nicotinamide in DMF (5 ml), and stirring was carried out for 30 min at RT. 445 mg (2.0 mmol) of 1-(2-chloroethylsulfonyl)-4-fluorobenzene were then added and stirring was continued for a further 2 days at RT. The mixture was then concentrated in vacuo, the residue was taken up in EA, and 1M aqueous NaHCO3 solution was added. The phases were separated and the aqueous phase was extracted with EA. The combined organic phases were dried over MgSO4, filtered through silica gel and concentrated in vacuo. CC (DCM/EA 4:1) of the residue yielded 365 mg (0.84 mmol, 48%) of 2-[2-(4-fluorophenyl)sulfonylethylthio]-N-(2-thienylmethyl)-nicotinamide. MS: m/z 437.0 [M+H]+
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08084470B2 |
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| Quelldatensatz | uspto-grants-2011_12 |
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| ORD ID | ord-107a00e5d1014a2d85e5395f9e05ba4b |
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| Quellennotiz | uspto-grants-2011_12 |
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