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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 345042Erstellt: 25. Oktober 2026

Methanesulfonyl chloride → N-(2-Methylquinolin-6-yl)methanesulfonamide

https://huagongshe.com/reaction/345042

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanesulfonyl chlorideHCID 31297—
Edukt2-Methylquinolin-6-amineHCID 103148—
LösungsmittelPyridineHCID 1049—
ProduktN-(2-Methylquinolin-6-yl)methanesulfonamideHCID 19813426—

Reaktionsschritte

Methanesulphonyl chloride (6.2 ml) was added dropwise to a stirred solution of 6-amino-2-methylquinoline (12.5 g) in pyridine (100 ml) cooled to 5°. Stirring was continued for 17 hours at room temperature. The pyridine was then removed by evaporation in vacuo, the residue diluted with aqueous sodium bicarbonate, and extracted three times with methylene chloride. The combined organic extracts were combined, dried (MgSO4) and evaporated in vacuo to give the title compound, yield 13.0 g, m.p. 151°-153°.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05055473
Quelldatensatzuspto-grants-1991_10
ORD IDord-791cb89a953e43a6977715154fc64535
Quellennotizuspto-grants-1991_10