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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 45263생성일: 2026년 10월 25일

p-Toluenesulfonic acid → 6-chloro-N-[(2,2-dimethyl-1,3-dioxolan-4-yl)methyl]-N-phenylpyridine-3-sulfonamide

https://huagongshe.com/reaction/45263

반응식

참여 물질

역할이름HCID투입량
반응물p-Toluenesulfonic acidHCID 6101—
반응물2,2-DimethoxypropaneHCID 6495—
반응물6-chloro-N-(2,3-dihydroxypropyl)-N-phenylpyridine-3-sulfonamideHCID 86659756—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물6-chloro-N-[(2,2-dimethyl-1,3-dioxolan-4-yl)methyl]-N-phenylpyridine-3-sulfonamideHCID 8665975773%

반응 단계

A mixture of 0.67 g (1.96 mmol) of 6-chloro-N-(2,3-dihydroxypropyl)-N-phenylpyridine-3-sulfonamide, 0.53 mL (4.3 mmol) of 2,2-dimethoxypropane and 37 mg of pTsOH in 4 mL of DMF is stirred for 3 hours at room temperature. The medium is taken up in 100 mL of EtOAc, washed with 50 mL of saturated NaHCO3 solution and 50 mL of water and then dried over Na2SO4, filtered and concentrated under reduced pressure. 0.54 g 6-chloro-N-[(2,2-dimethyl-1,3-dioxolan-4-yl)methyl]-N-phenylpyridine-3-sulfonamide is obtained in the form of a brown solid, which is used without further purification in the following step.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08541455B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-948e494dd4404503a7705e9713854a8a
출처 메모uspto-grants-2013_09