HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 389978Erstellt: 25. Oktober 2026
1-Hexanesulfonyl chloride → Hexane-1-sulfonic acid {5-[4-(2-trifluoromethylbenzoyl)piperazin-1-YL]pyridin-2-YL}amide
https://huagongshe.com/reaction/389978
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1-Hexanesulfonyl chloride | HCID 84504 | — |
| Edukt | [4-(6-Aminopyridin-3-YL)piperazin-1-YL]-(2-trifluoromethylphenyl)methanone | HCID 67419145 | — |
| Lösungsmittel | Pyridine | HCID 1049 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | Hexane-1-sulfonic acid {5-[4-(2-trifluoromethylbenzoyl)piperazin-1-YL]pyridin-2-YL}amide | HCID 11294961 | 8% |
Reaktionsschritte
To a solution of [4-(6-aminopyridin-3-yl)piperazin-1-yl]-(2-trifluoromethylphenyl)-methanone (0.035 g, 0.10 mmol) in pyridine (3 mL) was added hexanesulfonyl chloride (0.022 mL, 0.12 mmol). After heating at 60° C. for 20 h, the mixture was diluted with ethyl acetate (100 mL), washed with brine, dried over anhydrous MgSO4 and concentrated in vacuo. Purification by preparative thin layer chromatography afforded the title compound as a white solid (3.8 mg, 8% yield). 1H NMR (300 MHz, CDCl3) δ 7.66, 7.29, 4.08, 3.91, 3.38, 3.27, 3.08, 1.84, 1.35, 1.27, 0.87. MS (ES+) m/z 499.4 (M+1).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08383628B2 |
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| Quelldatensatz | uspto-grants-2013_02 |
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| ORD ID | ord-e33776045e6c44e9acbd26e6e6c5ac00 |
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| Quellennotiz | uspto-grants-2013_02 |
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