HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 925268Erstellt: 24. Oktober 2026
Cesium carbonate → 3-[[3,3-Difluoro-3-(4-fluorophenyl)-propyl]sulfanyl]-pyridine-4-carboxylic acid methyl ester
https://huagongshe.com/de/reaction/925268
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Cesium carbonate | HCID 10796 | — |
| Edukt | Methyl 3-chloroisonicotinate | HCID 15324397 | — |
| Edukt | 3,3-Difluoro-3-(4-fluorophenyl)-propane-1-thiol | HCID 86720162 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 3-[[3,3-Difluoro-3-(4-fluorophenyl)-propyl]sulfanyl]-pyridine-4-carboxylic acid methyl ester | HCID 86720165 | 34% |
Reaktionsschritte
To a solution of 3-chloro-pyridine-4-carboxylic acid methyl ester (0.28 g, 1.65 mmol) in DMF (10 ml) are added cesium carbonate (2.68 g, 8.25 mmol) and 3,3-difluoro-3-(4-fluorophenyl)-propane-1-thiol (synthesized according to the methods described in sections a) and b) of example 3) (0.34 g, 1.65 mmol) in a sealed tube. The reaction mixture is stirred at 90° C. for 1 h. After completion of the reaction, the mixture is diluted with water (15 ml) and extracted with EtOAc (3×20 ml). The organic layer is washed with water (20 ml), brine (20 ml), dried over anhydrous sodium sulfate and evaporated to get the crude product, which is purified by column chromatography (silica gel, 10% acetone/hexane) to yield 3-[[3,3-difluoro-3-(4-fluorophenyl)-propyl]sulfanyl]-pyridine-4-carboxylic acid methyl ester (0.19 g, 0.56 mmol, 34%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09284286B2 |
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| Quelldatensatz | uspto-grants-2016_03 |
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| ORD ID | ord-b879061a85c447d7833a3fb4f337e5e4 |
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| Quellennotiz | uspto-grants-2016_03 |
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