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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 69생성일: 2026년 10월 23일

2-Amino-N-methylbenzamide → 2-[2-Chloro-5-(trifluoromethyl)pyridin-4-ylamino]-N-methylbenzamide

https://huagongshe.com/ko/reaction/69

반응식

참여 물질

역할이름HCID투입량
반응물2-Amino-N-methylbenzamideHCID 308072—
반응물2-Chloro-4-iodo-5-(trifluoromethyl)pyridineHCID 2773791—
시약Cesium carbonateHCID 10796—
촉매1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
촉매Palladium (II) acetateHCID 4144353—
용매1,4-DioxaneHCID 31275—
생성물2-[2-Chloro-5-(trifluoromethyl)pyridin-4-ylamino]-N-methylbenzamideHCID 5665532863.41%

반응 조건

온도90 °C

반응 단계

2-chloro-4-iodo-5-(trifluoromethyl)pyridine (500 mg, 1.63 mmol), 2-amino-N- methylbenzamide (244 mg, 1.63 mmol), diacetoxypalladium (29.2 mg, 0.13 mmol), (9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine) (151 mg, 0.26 mmol) and cesium carbonate (636 mg, 1.95 mmol) were mixed together in dioxane (10 mL). Reaction was degassed with nitrogen and was stirred at 90 °C overnight under nitrogen. Reaction was filtered, washed with CH2Cl2 and filtrate was concentrated to dryness. The crude product was purified by flash chromatography on silica gel eluting with 10 to 50% ethyl acetate in petroleum ether. The solvent was evaporated to dryness to afford 2-(2-chloro-5-(trifluoromethyl)pyridin-4-ylamino)-N-methylbenzamide (340 mg, 63.4 %) as a pale yellow solid.

출처 및 근거

출처 데이터셋750 AstraZeneca ELN dataset
ORD IDord-59518020213f4a99980578b9463ad852
출처 메모750 AstraZeneca ELN dataset