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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | (E)-1-Bromo-4-(2-iodovinyl)benzene | HCID 12051842 | — |
| 반응물 | 4-Ethoxycarbonyl-N-benzoyliminopyridinium | HCID 86711217 | — |
| 촉매 | Silver(I) trifluoromethanesulfonate | HCID 76223 | — |
| 촉매 | Palladium bromide (PdBr2) | HCID 83469 | — |
| 용매 | 1,4-Dioxane | HCID 31275 | — |
| 생성물 | Ethyl 2-(4-bromophenyl)pyrazolo[1,5-a]pyridine-5-carboxylate | HCID 68276034 | 54% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09018395B2 |
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| 출처 데이터셋 | uspto-grants-2015_04 |
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| ORD ID | ord-8d9afb91e3aa4b77aed1ebcef3454d46 |
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| 출처 메모 | uspto-grants-2015_04 |
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