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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1622724생성일: 2026년 10월 27일

Ethanesulfonylchloride, 2-chloro- → 9-[4-(3-Ethylphenoxy)phenyl]-3,4-dihydropyrido[2,1-c][1,2,4]thiadiazine 2,2-dioxide

https://huagongshe.com/reaction/1622724

반응식

참여 물질

역할이름HCID투입량
반응물Ethanesulfonylchloride, 2-chloro-HCID 15385—
반응물Sodium hydrideHCID 24758—
반응물3-(4-(3-Ethylphenoxy)phenyl)pyridin-2-amineHCID 66748701—
용매TetrahydrofuranHCID 8028—
생성물9-[4-(3-Ethylphenoxy)phenyl]-3,4-dihydropyrido[2,1-c][1,2,4]thiadiazine 2,2-dioxideHCID 66748144—

반응 단계

To a suspension of NaH (60%, 215 mg) in THF (dry) (20 mL) was added 2-chloroethanesulfonyl chloride (0.339 mL) at 0° C. and the mixture was stirred for 5 min at the same temperature. A solution of 3-(4-(3-ethylphenoxy)phenyl)pyridin-2-amine (312 mg) in THF (dry) (30 mL) was added at 0° C. and the mixture was stirred at room temperature for 1 hr. The mixture was quenched with water at 0° C. Water and EtOAc/THF were added and the extracted organic layer was washed with brine. Silica-gel was added to the organic layer and the volatiles were removed in vacuo. The mixture supported on silica-gel was purified by column chromatography (NH silica gel, eluted with MeOH in EtOAc) and washed with IPE/EtOAc to give the title compound (295 mg) as a white solid. A part of this was recrystallized from THF/IPE.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08778934B2
출처 데이터셋uspto-grants-2014_07
ORD IDord-d5214fef3bea41b7b7cf7988427bbdcb
출처 메모uspto-grants-2014_07