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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1728888생성일: 2026년 10월 27일

Sodium Chloride → N-(2-Pyridinylmethyl)-N-[[4-(tetradecyloxy)phenyl]methyl]methanesulfonamide

https://huagongshe.com/reaction/1728888

반응식

참여 물질

역할이름HCID투입량
반응물Sodium ChlorideHCID 5234—
반응물Sodium hydrideHCID 24758—
반응물N-(pyridin-2-ylmethyl)methanesulfonamideHCID 4657001—
반응물1-(Bromomethyl)-4-(tetradecyloxy)benzeneHCID 10022840—
용매TetrahydrofuranHCID 8028—
생성물N-(2-Pyridinylmethyl)-N-[[4-(tetradecyloxy)phenyl]methyl]methanesulfonamideHCID 1901498638.3%

반응 단계

To a room temperature slurry of 0.391 g of 50% sodium hydride in 20 ml of dry tetrahydrofuran is added, via cannula, 1.27 g of product from Example 121 in 30 ml of dry tetrahydrofuran. The reaction is stirred at room temperature for 1.5 hours. Two and one half grams of product from Example 20 in 30 ml of dry tetrahydrofuran is added via cannula. The reaction is stirred at room temperature for 20 hours followed by heating at reflux temperature for 2 hours. The cooled reaction is poured into half saturated sodium chloride and extracted with methylene chloride. The combined organic layers are washed with saturated sodium chloride, dried and concentrated in vacuo. The residue is purified by chromatography (silica gel: 40% ethyl acetate/hexane) to give 1.22 g of the desired product as colorless crystals.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05328921
출처 데이터셋uspto-grants-1994_07
ORD IDord-abeb253751d443a4ba7a9229a3cea3cb
출처 메모uspto-grants-1994_07