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HRID 13425생성일: 2026년 10월 24일

Picolinic acid → N-(3-fluoro-4-(3-methyl-3-butenoyl)phenyl)pyridine-2-carboxamide

https://huagongshe.com/ko/reaction/13425

반응식

참여 물질

역할이름HCID투입량
반응물Picolinic acidHCID 1018—
반응물TetrahydrofuranHCID 8028—
반응물N-(3-fluoro-4-((methoxy(methyl)amino)carbonyl)phenyl)pyridine-2-carboxamideHCID 23145523—
반응물HCID 178448200HCID 178448200—
용매WaterHCID 962—
생성물N-(3-fluoro-4-(3-methyl-3-butenoyl)phenyl)pyridine-2-carboxamideHCID 23145243—

반응 단계

9.89 ml of (2-methyl-2-propen-1-yl)magnesium chloride (0.50 M tetrahydrofuran solution) was added to a tetrahydrofuran (10 ml) solution of 500 mg of N-(3-fluoro-4-((methoxy(methyl)amino)carbonyl)phenyl)pyridine-2-carboxamide obtained in the same method as in Example 145 (step 3) or in accordance with the method or by combining it with an ordinary method but using pyridine-2-carboxylic acid, with cooling with ice. The reaction liquid was stirred for 3 hours with cooling with ice, and then water was poured into the reaction solution, extracted with ethyl acetate and dried with anhydrous sodium sulfate. The solvent was evaporated away under reduced pressure, and the resulting residue was purified through silica gel column chromatography (developing solvent: hexane/ethyl acetate=3/1) to obtain the entitled compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728025B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-9581c41b61054aff8661bb529241a2ff
출처 메모uspto-grants-2010_06