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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 876403생성일: 2026년 10월 24일

8-(Tert-butyldimethylsilyloxy)-2-((2-(4-(2-methoxyethoxy)pyridin-2-yl)hydrazono)methyl)quinoline → 8-(Tert-butyldimethylsilyloxy)-2-(7-(2-methoxyethoxy)-[1,2,4]triazolo[4,3-a]pyridin-3-yl)quinoline

https://huagongshe.com/ko/reaction/876403

반응식

참여 물질

역할이름HCID투입량
반응물8-(Tert-butyldimethylsilyloxy)-2-((2-(4-(2-methoxyethoxy)pyridin-2-yl)hydrazono)methyl)quinolineHCID 67229769—
반응물Acetic acid;iodosylbenzeneHCID 73357407—
용매DichloromethaneHCID 6344—
생성물8-(Tert-butyldimethylsilyloxy)-2-(7-(2-methoxyethoxy)-[1,2,4]triazolo[4,3-a]pyridin-3-yl)quinolineHCID 6723122570%

반응 단계

To a solution of 8-(tert-butyldimethylsilyloxy)-2-((2-(4-(2-methoxyethoxy)pyridin-2-yl)hydrazono)methyl)quinoline (0.101 g, 0.223 mmol) in DCM (1.0 mL) was added iodosobenzene diacetate (0.0719 g, 0.223 mmol). After stirring at ambient temperature for 5 hours the reaction mixture was partitioned between DCM and aqueous saturated Na2S2O3. The organic layer was washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The residue was purified by flash column chromatography (40:1 DCM/MeOH) to provide 70 mg (70%) of desired product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08987251B2
출처 데이터셋uspto-grants-2015_03
ORD IDord-4cf61e3655e64da39eee9a444395c8cb
출처 메모uspto-grants-2015_03