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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1521332생성일: 2026년 10월 25일

Acetic Acid → 4-fluoro-3-(7-(1-methyl-1H-pyrazol-5-yl)imidazo[1,2-a]pyridine-3-carboxamido)benzoic acid

https://huagongshe.com/reaction/1521332

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물1-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazoleHCID 2760077—
반응물3-[(7-Bromo-imidazo[1,2-a]pyridine-3-carbonyl)-amino]-4-fluoro-benzoic Acid Methyl EsterHCID 71282888—
촉매HCID 178418807HCID 178418807—
용매Sodium CarbonateHCID 10340—
용매1,4-DioxaneHCID 31275—
생성물4-fluoro-3-(7-(1-methyl-1H-pyrazol-5-yl)imidazo[1,2-a]pyridine-3-carboxamido)benzoic acidHCID 71282909—

반응 조건

온도50 °C

반응 단계

3-[(7-Bromo-imidazo[1,2-a]pyridine-3-carbonyl)-amino]-4-fluoro-benzoic acid methyl ester (step 1) (1200 g, 3.060 mol), 1-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (commercially available) (764 g, 3.67 mol), PdCl2(dppf)•CH2Cl2 (75.0 g, 91.8 mmol) in dioxane (10 L) and aqueous Na2CO3 (2 N, 4.6 L) were heated to reflux for 6 hr. The reaction mixture was cooled to 50° C. and filtered. The filtrate was heated to reflux, to which was added AcOH (600 g, 10.0 mol) was added dropwise. During the course of addition solids came out of solution to give pale pink slurry. After addition the mixture was slowly cooled to RT and filtered. To the filter cake was added dioxane (20 L) followed by heating to reflux to obtain a solution. The solution was cooled to RT and filtered to provide the title compound as a white solid;

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09073921B2
출처 데이터셋uspto-grants-2015_07
ORD IDord-e78e337ad4fc4a4fbda47634f408b91c
출처 메모uspto-grants-2015_07