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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 748518생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/748518

반응식

참여 물질

역할이름HCID투입량
반응물Methyl(2-(pyrrolidin-1-yl)ethyl)amineHCID 295976—
반응물2-Chloro-5-pyridinesulfonyl chlorideHCID 2792792—
용매DichloromethaneHCID 6344—
생성물6-Chloro-N-methyl-N-(2-pyrrolidin-1-ylethyl)pyridine-3-sulfonamideHCID 6320744482.3%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07399780B2
출처 데이터셋uspto-grants-2008_07
ORD IDord-f74ad4236f434ba7ac93b1a8c2dd5aec
출처 메모uspto-grants-2008_07