HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 530916Erstellt: 26. Oktober 2026
Ammonia → 2-(3-ethylsulfanyl-pyridin-2-yl)-1-methyl-5-pentafluoroethyl-1H-benzimidazole
https://huagongshe.com/reaction/530916
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ammonia | HCID 222 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | Sodium pentafluoropropionate | HCID 2733305 | — |
| Edukt | 2-(3-ethylsulfanyl-pyridin-2-yl)-5-iodo-1-methyl-1H-benzimidazole | HCID 71247076 | — |
| Katalysator | Copper iodide | HCID 83717 | — |
| Lösungsmittel | O-Xylene | HCID 7237 | — |
| Lösungsmittel | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Produkt | 2-(3-ethylsulfanyl-pyridin-2-yl)-1-methyl-5-pentafluoroethyl-1H-benzimidazole | HCID 86725177 | 72% |
Reaktionsschritte
A mixture of 2-(3-ethylsulfanyl-pyridin-2-yl)-5-iodo-1-methyl-1H-benzimidazole (340 mg), copper iodide (410 mg), sodium pentafluoropropionate (800 mg), NMP (5 ml), and xylene (5 ml) was stirred at 160° C. for 5 hours. The reaction mixture was allowed to cool to room temperature, and then saturated aqueous sodium hydrogen carbonate solution and 26% ammonia solution were poured thereto. Then, the mixture was extracted with t-butylmethyl ether. The organic layer was dried over sodium sulfate, and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to give 2-(3-ethylsulfanyl-pyridin-2-yl)-1-methyl-5-pentafluoroethyl-1H-benzimidazole (240 mg), which is hereinafter referred to as “the present compound 26”.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09353110B2 |
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| Quelldatensatz | uspto-grants-2016_05 |
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| ORD ID | ord-4111157bdfd448fe9cf728f8942e8202 |
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| Quellennotiz | uspto-grants-2016_05 |
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