돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1748008생성일: 2026년 10월 26일

Ethanesulfonylchloride, 2-chloro- → 9-(4-((Tert-butyl(dimethyl)silyl)oxy)phenyl)-3,4-dihydropyrido[2,1-c][1,2,4]thiadiazine 2,2-dioxide

https://huagongshe.com/reaction/1748008

반응식

참여 물질

역할이름HCID투입량
반응물Ethanesulfonylchloride, 2-chloro-HCID 15385—
반응물Sodium hydrideHCID 24758—
반응물3-(4-((Tert-butyl(dimethyl)silyl)oxy)phenyl)pyridin-2-amineHCID 66747707—
용매TetrahydrofuranHCID 8028—
생성물9-(4-((Tert-butyl(dimethyl)silyl)oxy)phenyl)-3,4-dihydropyrido[2,1-c][1,2,4]thiadiazine 2,2-dioxideHCID 66747725—

반응 단계

To a suspension of NaH (60%, 42.0 g) in THF (dry) (350 mL) was added 2-chloroethanesulfonyl chloride (44.5 mL) at 0° C. and the mixture was stirred for 10 min at the same temperature. A solution of 3-(4-((tert-butyl(dimethyl)silyl)oxy)phenyl)pyridin-2-amine (78.8 g) in THF (dry) (350 mL) was added at 0° C. and the mixture was stirred at room temperature under N2 overnight. The mixture was quenched with water at 0° C. carefully. Additional water was added to form precipitates which were washed with water and EtOAc and collected to give the title compound (65.5 g) as an off-white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09150591B2
출처 데이터셋uspto-grants-2015_10
ORD IDord-578e488008ca4f13bebbaf74e9cc7000
출처 메모uspto-grants-2015_10