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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 708978생성일: 2026년 10월 25일

Cesium carbonate → 1-[(6-Chloro-3-pyridyl)methyl]-3-(3-cyanophenyl)-4-oxo-pyrido[1,2-a]pyrimidin-1-ium-2-olate

https://huagongshe.com/reaction/708978

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물3-Cyanophenylboronic acidHCID 2734325—
반응물Tri-tert-butylphosphine tetrafluoroborateHCID 2734635—
반응물1-[(6-Chloro-3-pyridyl)methyl]-3-iodo-4-oxo-pyrido[1,2-a]pyrimidin-1-ium-2-olateHCID 86709267—
촉매palladium(II) acetateHCID 167845—
용매1,4-DioxaneHCID 31275—
용매Dichloromethane methanolHCID 21226129—
생성물1-[(6-Chloro-3-pyridyl)methyl]-3-(3-cyanophenyl)-4-oxo-pyrido[1,2-a]pyrimidin-1-ium-2-olateHCID 86709269—

반응 조건

온도80 °C

반응 단계

To a mixture of 80 mg (0.54 mmol) (3-cyanophenyl)boronic acid, 150 mg (0.36 mmol) 1-[(6-chloro-3-pyridyl)methyl]-3-iodo-4-oxo-pyrido[1,2-a]pyrimidin-1-ium-2-olate (Synthesis described in WO 2009/099929), 1.6 mg (0.07 mmol) palladium acetate, 21 mg (0.07 mmol) tri-tert-butylphosphonium tetrafluoroborate and 295 mg caesium carbonate was added 50 ml of dioxane under argon. The mixture was heated to 80° C. for 48 hours. Silica was added and the product was obtained by column chromatographie (dichloromethane/methanol) (21 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09179680B2
출처 데이터셋uspto-grants-2015_11
ORD IDord-4fca8d19709242a3a3a619ccb8817289
출처 메모uspto-grants-2015_11