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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2355781Erstellt: 26. Oktober 2026

Pyridine → E 7820

https://huagongshe.com/reaction/2355781

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
Edukt3-Cyanobenzene-1-sulfonyl chlorideHCID 2801360—
Edukt7-amino-4-methyl-1H-indole-3-carbonitrileHCID 11715247—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktE 7820HCID 19697047,4%

Reaktionsschritte

To a solution of 7-amino-3-cyano-4-methyl-1H-indole (10 g, 58.4 mmol) in tetrahydrofuran (200 ml) were added pyridine (20 ml) and 3-cyanobenzenesulfonyl chloride (12.5 g), followed by stirring at room temperature for 3.5 hours. After further adding 2N hydrochloric acid (100 ml), extraction was performed with ethyl acetate. The organic layer was washed with water (twice) and brine in that order, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=2:1-3:2). A mixed solvent of ethanol-hexane (1:2) was added thereto, and after sonication, the precipitate was collected by filtration and washed with a mixed solvent of ethanol-hexane (1:3). The mixture was dried overnight under reduced pressure to give the title compound (9.33 g, 27.7 mmol, 47% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07754894B2
Quelldatensatzuspto-grants-2010_07
ORD IDord-a1376e18842647db882858a5a7bf7bda
Quellennotizuspto-grants-2010_07