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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetonitrileHCID 6342—
Edukt3-Methyl-2-butanolHCID 11732—
Edukt4-fluoro-N-(5-isopropylpyridin-2-yl)benzenesulfonamideHCID 89875926—
LösungsmittelTolueneHCID 1140—
Produkt4-fluoro-N-(5-isopropylpyridin-2-yl)-N-(3-methylbutan-2-yl)benzenesulfonamideHCID 8987625212,7%

Reaktionsbedingungen

Temperatur150 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09242972B2
Quelldatensatzuspto-grants-2016_01
ORD IDord-f81f74f41e2942be813ef9ad80443cdc
Quellennotizuspto-grants-2016_01