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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1475934생성일: 2026년 10월 27일

(E)-1-Bromo-4-(2-iodovinyl)benzene → Ethyl 2-(4-bromophenyl)pyrazolo[1,5-a]pyridine-5-carboxylate

https://huagongshe.com/reaction/1475934

반응식

참여 물질

역할이름HCID투입량
반응물(E)-1-Bromo-4-(2-iodovinyl)benzeneHCID 12051842—
반응물4-Ethoxycarbonyl-N-benzoyliminopyridiniumHCID 86711217—
촉매Silver(I) trifluoromethanesulfonateHCID 76223—
촉매Palladium bromide (PdBr2)HCID 83469—
용매1,4-DioxaneHCID 31275—
생성물Ethyl 2-(4-bromophenyl)pyrazolo[1,5-a]pyridine-5-carboxylateHCID 6827603454%

반응 조건

온도127.5 °C

반응 단계

Related procedures are described in Org. Lett. 2010, 12, 516): 4-Ethoxycarbonyl-N-benzoyliminopyridinium ylid (JOC 2003, 68, 7119) (3.50 g, 13.0 mmol), para-tris-methoxyphenylphosphine (686 mg, 1.95 mmol), Palladium (II) bromide (173 mg, 0.65 mmol), silver triflate (8.93 g, 39.0 mmol) and (E)-1-Bromo-4-(2-iodovinyl)benzene (Org. Lett. 2008, 10, 5485) (4.02 g, 13.0 mmol) were placed in a 250 mL round bottom flask equipped a with magnetic stirrer. Dioxane (52 mL) was added. The mixture was degassed by bubbling nitrogen for 10 minutes with vigorous stirring and heated to 125-130° C. for 15-20 h. The mixture was then cooled to room temperature, diluted with CH2Cl2, filtered over Celite. The organic layer was then washed with saturated aqueous sodium bicarbonate and the organic phase was concentrated under reduced pressure. The crude product was triturated with methanol to afford 2.40 g (54%) of the title compound. LCMS m/z 345.0, 347.0 (M+H)+, ret. time=3.05 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09018395B2
출처 데이터셋uspto-grants-2015_04
ORD IDord-8d9afb91e3aa4b77aed1ebcef3454d46
출처 메모uspto-grants-2015_04