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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 748518Erstellt: 24. Oktober 2026

Methyl(2-(pyrrolidin-1-yl)ethyl)amine → 6-Chloro-N-methyl-N-(2-pyrrolidin-1-ylethyl)pyridine-3-sulfonamide

https://huagongshe.com/de/reaction/748518

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl(2-(pyrrolidin-1-yl)ethyl)amineHCID 295976—
Edukt2-Chloro-5-pyridinesulfonyl chlorideHCID 2792792—
LösungsmittelDichloromethaneHCID 6344—
Produkt6-Chloro-N-methyl-N-(2-pyrrolidin-1-ylethyl)pyridine-3-sulfonamideHCID 6320744482,3%

Reaktionsschritte

To a solution of 6-chloropyridine-3-sulfonylchloride (636 mg, 3 mmol; described in: Naegeli, C. et al. Helv. Chim. Actal. 1938, 21, 1746-1750) in methylene chloride (10 mL) was added methyl-(2-pyrrolidin-1-ylethyl)amine (384 mg, 3 mmol; described in: J. Amer. Chem. Soc. 1955, 77, 3632-3634) dissolved in methylene chloride (10 mL) dropwise. The reaction mixture was stirred over night at room temperature followed by the extraction with aqueous HCl (3%). The acidic water layer was alkalized with an aqueous saturated solution of NaHCO3 and extracted with methylene chloride. The organic phase was dried (Na2SO4) and evaporated in vacuo to give 0.75 gram (80% yield) of the title compound: MS (ES) m/z 304 (M++1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07399780B2
Quelldatensatzuspto-grants-2008_07
ORD IDord-f74ad4236f434ba7ac93b1a8c2dd5aec
Quellennotizuspto-grants-2008_07