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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 526646생성일: 2026년 10월 24일

Sodium Bicarbonate → 6-(4-(4-cyano-3-methylphenyl)-5-methoxy-1H-pyrazol-1-yl)-N-(3-methoxypropyl)nicotinamide

https://huagongshe.com/ko/reaction/526646

반응식

참여 물질

역할이름HCID투입량
반응물Sodium BicarbonateHCID 516892—
반응물2-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrileHCID 45158520—
반응물6-(4-bromo-5-methoxy-1H-pyrazol-1-yl)-N-(3-methoxypropyl)nicotinamideHCID 117601269—
촉매HCID 178454869HCID 178454869—
용매WaterHCID 962—
용매1,4-DioxaneHCID 31275—
생성물6-(4-(4-cyano-3-methylphenyl)-5-methoxy-1H-pyrazol-1-yl)-N-(3-methoxypropyl)nicotinamideHCID 117601399—

반응 단계

Combined 6-(4-bromo-5-methoxy-1H-pyrazol-1-yl)-N-(3-methoxypropyl)nicotinamide (50 mg, 0.135 mmol), 2-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrile (65.8 mg, 0.271 mmol), [1,1′-bis(di-tert-butylphosphino) ferrocene]dichloropalladium(II) (13.86 mg, 0.021 mmol) and sodium bicarbonate (56.9 mg, 0.677 mmol) in dioxane (599 μl) and water (150 μl) was heated at 110° C. in the microwave for 40 minutes. The reaction mixture was filtered through Celite® and concentrated in vacuo to give 6-(4-(4-cyano-3-methylphenyl)-5-methoxy-1H-pyrazol-1-yl)-N-(3-methoxypropyl)nicotinamide which was used in next step without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09345713B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-8a5eca89808a4e7db5f8ae77564979b1
출처 메모uspto-grants-2016_05