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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 79180생성일: 2026년 10월 24일

1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine) → 5-(4-(2-(t-Butyldimethylsilyloxy)ethyl)piperidin-1-yl)-2-chloropyridine

https://huagongshe.com/ko/reaction/79180

반응식

참여 물질

역할이름HCID투입량
반응물1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
반응물2-Chloro-5-iodopyridineHCID 4397176—
반응물4-Piperidineethanol TBSHCID 16220759—
반응물Sodium t-butoxideHCID 23676156—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매1,4-DioxaneHCID 31275—
생성물5-(4-(2-(t-Butyldimethylsilyloxy)ethyl)piperidin-1-yl)-2-chloropyridineHCID 5829984340.2%

반응 조건

온도80 °C

반응 단계

2-chloro-5-iodopyridine (1.00 g, 4.18 mmol), compound 292 (1.02 g, 4.18 mmol), Tris(dibenzylideneacetone)dipalladium (0) (0.191 g, 0.209 mmol), 4,5-bis(diphenylphosphino)-9,9-dimethyl-9H-xanthene (0.242 g, 0.418 mmol), and sodium t-butoxide (0.803 g, 8.35 mmol) were dissolved in 20 mL dioxane. The reaction was purged with argon and heated at 80° C. for 16 hours. The solvent was removed in vacuo and silica gel chromatography (gradient elution hexanes/0-10% ethyl acetate) afforded compound 293 as a beige solid (597 mg, 40%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841312B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-894b6f7d240e44efa386e0555428b34d
출처 메모uspto-grants-2014_09