돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 9185생성일: 2026년 10월 24일

Ethyl Acetate → 7-(2-Chloro-4-methoxyphenyl)-2-ethyl-3-nitropyrazolo[1,5-a]pyridine

https://huagongshe.com/ko/reaction/9185

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물Barium hydroxide, octahydrateHCID 17749109—
반응물7-Bromo-2-ethyl-3-nitropyrazolo[1,5-a]pyridineHCID 21984481—
반응물2-Chloro-4-methoxyphenylboric acidHCID 21984696—
촉매HCID 178418397HCID 178418397—
용매WaterHCID 962—
용매1,2-DimethoxyethaneHCID 8071—
생성물7-(2-Chloro-4-methoxyphenyl)-2-ethyl-3-nitropyrazolo[1,5-a]pyridineHCID 2198458373.3%

반응 조건

온도80 °C

반응 단계

After dissolving 7-bromo-2-ethyl-3-nitropyrazolo[1,5-a]pyridine (100 mg) in 1,2-dimethoxyethane (6 mL) and water (1 mL), 2-chloro-4-methoxyphenylboric acid (138 mg), tetrakis(triphenylphosphine)palladium (0) complex (86 mg) and barium hydroxide octahydrate (233 mg) were added and the mixture was heated and stirred at 80° C. for 3 hours under a nitrogen stream. Water was added to the reaction mixture, extraction was performed with ethyl acetate and the extract was washed with saturated aqueous sodium hydrogencarbonate and brine, in that order. After drying over anhydrous magnesium sulfate and filtration, the solvent was concentrated under reduced pressure, the residue was purified by silica gel column chromatography, and the title compound (90 mg) was obtained from the n-hexane:ethyl acetate (30:1) fraction as yellow crystals.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091215B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-9528c738ae574cb594267acce885900b
출처 메모uspto-grants-2006_08