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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1446675생성일: 2026년 10월 26일

Potassium Carbonate → 4-[4-(7-Chloro-imidazo[1,2-a]pyridin-3-yl)-phenyl]-N-(3-trifluoromethyl-phenyl)-butyramide

https://huagongshe.com/reaction/1446675

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물7-Chloro-3-iodoimidazo[1,2-a]pyridineHCID 57497697—
반응물4-[4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-N-(3-trifluoromethyl-phenyl)-butyramideHCID 68546073—
촉매HCID 178418476HCID 178418476—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
용매1,4-DioxaneHCID 31275—
생성물4-[4-(7-Chloro-imidazo[1,2-a]pyridin-3-yl)-phenyl]-N-(3-trifluoromethyl-phenyl)-butyramideHCID 6854283262.6%

반응 단계

Suspend 4-[4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-N-(3-trifluoromethyl-phenyl)-butyramide (0.47 g, 1.15 mmol), 7-chloro-3-iodo-imidazo[1,2-a]pyridine (0.29 g, 1.05 mmol) and solid potassium carbonate (0.48 g, 3.45 mmol) in dioxane (4 mL) and water (2 mL). Deoxygenate the reaction contents with nitrogen for 10 minutes at room temperature. Add trans-dichlorobis(triphenylphosphine)palladium (II) (22 mg, 0.03 mmol) to the reaction. Fit a reflux condenser and heat the reaction to 105° C. over the weekend. Cool the reaction, dilute with dichloromethane and filter through Celite®. Concentrate the filtrate and then chromatograph on silica, using 0-3% methanol/ethyl acetate, to yield the product (301 mg, 57%). MS(ES), m/z 458 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07666879B2
출처 데이터셋uspto-grants-2010_02
ORD IDord-66b40ce91cb54be4a6ddfcea1e681aaa
출처 메모uspto-grants-2010_02