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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2216369생성일: 2026년 10월 26일

Dimethyl Sulfoxide → 2-Bromo-6-(3,3-ethylenedioxypyrrolidine-1-yl)pyridine

https://huagongshe.com/reaction/2216369

반응식

참여 물질

역할이름HCID투입량
반응물Dimethyl SulfoxideHCID 679—
반응물TriethylamineHCID 8471—
반응물Oxalyl chlorideHCID 65578—
반응물1-(6-Bromopyridin-2-yl)pyrrolidin-3-olHCID 21942298—
용매DichloromethaneHCID 6344—
생성물2-Bromo-6-(3,3-ethylenedioxypyrrolidine-1-yl)pyridineHCID 21942269—

반응 단계

Then, to a solution of 2.8 ml of oxalyl chloride in 100 ml of dichloromethane were added dropwise 4.6 ml of dimethyl sulfoxide in a dry ice-acetone bath while stirring, a solution of 5.9 g of the 2-bromo-6-(3-hydroxypyrrolidin-1-yl)pyridine in 50 ml of dichloromethane and finally 17 ml of triethylamine, and the temperature was returned to room temperature over 1 hour. The reaction mixture was washed with water and brine, dried over anhydrous magnesium sulfate and concentrated. To the residue were added 50 ml of toluene, 7 ml of ethylene glycol and a catalytic amount of p-toluenesulfonic acid monohydrate, followed by heating under reflux for 3 hours while removing water. After cooling, it was washed with a saturated aqueous sodium hydrogen carbonate solution and brine, dried over anhydrous magnesium sulfate and concentrated. The residue was subjected to silica gel column chromatography with 5–7% ethyl acetate/hexane, to give 6.3 g of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07112593B2
출처 데이터셋uspto-grants-2006_09
ORD IDord-d67ea716eea54e9bad51dd631d644cf9
출처 메모uspto-grants-2006_09