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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 584생성일: 2026년 10월 24일

4-Fluoro-N-methylaniline → methyl 2-(4-fluoro-N-methylanilino)pyridine-4-carboxylate

https://huagongshe.com/ko/reaction/584

반응식

참여 물질

역할이름HCID투입량
반응물4-Fluoro-N-methylanilineHCID 68024—
반응물2-Bromo-isonicotinic acid methyl esterHCID 3847768—
시약Cesium carbonateHCID 10796—
촉매2-(Dicyclohexylphosphino)biphenylHCID 2734216—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매TolueneHCID 1140—
생성물methyl 2-(4-fluoro-N-methylanilino)pyridine-4-carboxylateHCID 1083792060%

반응 조건

온도105 °C

반응 단계

In a 100 mL round-bottomed flask (t=g) was methyl 2-bromoisonicotinate (.5 g, 2.31 mmol), 4-fluoro-N-methylaniline (0.348 g, 2.78 mmol), and CS2CO3 (1.056 g, 3.24 mmol) in toluene (16 mL) to give a yellow suspension. Pd2dba3 (0.106 g, 0.12 mmol) and biphenyl-2-yldicyclohexylphosphine (0.122 g, 0.35 mmol) were added. Reaction was allowed to stir overnight. LC/MS in the morning revealed little product had formed. Something with mass 272 dominated. Reaction was discarded.

출처 및 근거

출처 데이터셋750 AstraZeneca ELN dataset
ORD IDord-3a62166a30464afb9cbe502b267cbcba
출처 메모750 AstraZeneca ELN dataset