HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 594120Erstellt: 27. Oktober 2026
Acetonitrile → 4-fluoro-N-(5-isopropylpyridin-2-yl)-N-(3-methylbutan-2-yl)benzenesulfonamide
https://huagongshe.com/reaction/594120
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Acetonitrile | HCID 6342 | — |
| Edukt | 3-Methyl-2-butanol | HCID 11732 | — |
| Edukt | 4-fluoro-N-(5-isopropylpyridin-2-yl)benzenesulfonamide | HCID 89875926 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 4-fluoro-N-(5-isopropylpyridin-2-yl)-N-(3-methylbutan-2-yl)benzenesulfonamide | HCID 89876252 | 12,7% |
Reaktionsschritte
To a solution of 4-fluoro-N-(5-isopropylpyridin-2-yl)benzenesulfonamide (203 mg, 0.690 mmol) and 3-methylbutan-2-ol (60.8 mg, 0.690 mmol) in toluene (3 mL) stirred in air at room temperature was added a solution of 2-tributylphosphoranylidene)acetonitrile (166 mg, 0.690 mmol) in toluene (0.5 mL). The reaction vessel was sealed and heated by microwaves to 150° C. for 30 minutes. After cooling, the solvent was evaporated in vacuo and the crude purified by mass directed autoprep (formic acid modifier) to give the title product (32 mg) as a colourless oil. LCMS (2 min, formic) Rt 1.41 min, m/z (ES+) 365 (M+H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09242972B2 |
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| Quelldatensatz | uspto-grants-2016_01 |
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| ORD ID | ord-f81f74f41e2942be813ef9ad80443cdc |
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| Quellennotiz | uspto-grants-2016_01 |
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