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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 487331Erstellt: 23. Oktober 2026

Methyl iodide → 6-(4-(2-(N-Methyl-4-chlorobenzenesulphonylamino)ethyl)phenyl)-6-(3-pyridyl)hex-5-enoic acid

https://huagongshe.com/de/reaction/487331

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl iodideHCID 6328—
EduktDichloromethaneHCID 6344—
Edukt6-(4-(2-(4-Chlorobenzenesulphonylamino)ethyl)-phenyl)-6-(3-pyridyl)hex-5-enoic acidHCID 65971—
KatalysatorBenzyltrimethylammonium chlorideHCID 5963—
LösungsmittelSodium HydroxideHCID 14798—
Produkt6-(4-(2-(N-Methyl-4-chlorobenzenesulphonylamino)ethyl)phenyl)-6-(3-pyridyl)hex-5-enoic acidHCID 54262804—

Reaktionsschritte

2.0 g of 6-(4-(2-(4-chlorobenzenesulphonylamino)ethyl)-phenyl)-6-(3-pyridyl)hex-5-enoic acid are stirred overnight in 10 ml of 4N sodium hydroxide solution, 100 ml of methylene chloride, 80 mg of benzyl trimethylammonium chloride and 0.85 g of methyl iodide. Then the organic phase is separated off and the aqueous phase is acidified to pH 5. The product precipitated is separated off and taken up in methylene chloride, dried and evaporated down. Finally, the residue is chromatographed with ethylene chloride/methanol (97:3) over a silica gel column.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05294626
Quelldatensatzuspto-grants-1994_03
ORD IDord-5bd35299ab28429799ed76c9d3dd6466
Quellennotizuspto-grants-1994_03