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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1181906생성일: 2026년 10월 27일

Water → N-[7-(2-Methoxy-4,6-dimethylphenyl)-2-(methylsulfanyl)pyrazolo[1,5-a]pyridin-3-yl]-N-(2-pyridyl)amine

https://huagongshe.com/reaction/1181906

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물2-BromopyridineHCID 7973—
반응물7-(2-Methoxy-4,6-dimethylphenyl)-2-(methylsulfanyl)pyrazolo[1,5-a]pyridine-3-amineHCID 21984486—
반응물Sodium t-butoxideHCID 23676156—
용매TolueneHCID 1140—
생성물N-[7-(2-Methoxy-4,6-dimethylphenyl)-2-(methylsulfanyl)pyrazolo[1,5-a]pyridin-3-yl]-N-(2-pyridyl)amineHCID 21984615—

반응 조건

온도120 °C

반응 단계

After dissolving [7-(2-methoxy-4,6-dimethylphenyl)-2-(methylsulfanyl)pyrazolo[1,5-a]pyridin-3-yl]amine (40 mg) in toluene (1 mL), 2-bromopyridine (0.013 mL), sodium t-butoxide (25 mg) and dichlorobis(tri-o-tolylphosphine)palladium complex (3 mg) were added and the mixture was heated and stirred at 120° C. for 5 hours. The mixture was cooled to room temperature, water was added, and extraction was performed with ethyl acetate. The organic layer was washed with brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography, and the title compound (12 mg) was obtained from the ethyl acetate:n-hexane (1:2) fraction as white crystals.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07285666B2
출처 데이터셋uspto-grants-2007_10
ORD IDord-2c125486dbe44dd69df42bb5c4ab0fb4
출처 메모uspto-grants-2007_10