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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1582064생성일: 2026년 10월 27일

Triethylamine → 2-(N-methanesulfonyl-4-piperidinyloxy)-5-chloropyridine

https://huagongshe.com/reaction/1582064

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Methanesulfonyl chlorideHCID 31297—
반응물5-Chloro-2-(piperidin-4-yloxy)pyridineHCID 11264329—
용매DichloromethaneHCID 6344—
생성물2-(N-methanesulfonyl-4-piperidinyloxy)-5-chloropyridineHCID 2271971986.6%

반응 단계

To a solution 2-(4-piperidinyloxy)-5-chloropyridine(12.9 g, 0.06 mol) and Et3N (25.4 ml, 0.182 mol) in dry dichloromethane (400 ml) at 0° C. and under Argon, was added methanesulfonyl chloride (5.3 ml, 0.067 mol) in dry dichloromethane (100 ml), dropwise. The mixture was stirred for 20 hours at room temperature. The mixture was diluted with dichloromethane (250 ml), then washed with water (×3) then brine. The organic layers were dried with Na2SO4 and evaporated in vacuo. The residue was triturated and washed with diethylether to give 2-(N-methanesulfonyl-4-piperidinyloxy)-5-chloropyridine (15.1 g) as a pale yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06734184B1
출처 데이터셋uspto-grants-2004_05
ORD IDord-97ee7243a24d4f11b155705a57c6c212
출처 메모uspto-grants-2004_05