Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 748518Generated: October 25, 2026

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

https://huagongshe.com/reaction/748518

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl(2-(pyrrolidin-1-yl)ethyl)amineHCID 295976—
Reactant2-Chloro-5-pyridinesulfonyl chlorideHCID 2792792—
SolventDichloromethaneHCID 6344—
Product6-Chloro-N-methyl-N-(2-pyrrolidin-1-ylethyl)pyridine-3-sulfonamideHCID 6320744482.3%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07399780B2
Source datasetuspto-grants-2008_07
ORD IDord-f74ad4236f434ba7ac93b1a8c2dd5aec
Source noteuspto-grants-2008_07