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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 418994생성일: 2026년 10월 24일

N-Methoxy-6,N-dimethyl-nicotinamide → 4-Chloro-N-[5-chloro-2-(6-methyl-pyridine-3-carbonyl)-pyridin-3-yl]-N-methoxymethyl-3-trifluoromethyl-benzenesulfonamide

https://huagongshe.com/ko/reaction/418994

반응식

참여 물질

역할이름HCID투입량
반응물N-Methoxy-6,N-dimethyl-nicotinamideHCID 11367353—
반응물N-(2-Bromo-5-chloro-pyridin-3-yl)-4-chloro-N-methoxvmethyl-3-trifluoromethyl-benzenesulfonamideHCID 57942086—
반응물HCID 178418918HCID 178418918—
용매TetrahydrofuranHCID 8028—
생성물4-Chloro-N-[5-chloro-2-(6-methyl-pyridine-3-carbonyl)-pyridin-3-yl]-N-methoxymethyl-3-trifluoromethyl-benzenesulfonamideHCID 5794255433.7%

반응 조건

온도-78 °C

반응 단계

To a solution of N-(2-bromo-5-chloro-pyridin-3-yl)-4-chloro-N-methoxymethyl-3-trifluoromethyl-benzenesulfonamide (90 mg, 0.2 mmol) in 2.0 mL of THF under nitrogen atmosphere at −78° C. was added drop-wise 0.3 mL (0.6 mmol) of isopropylmagnesium chloride. The mixture was then stirred for 10 min at −78° C. followed by warming to room temperature and stirred at that temperature for 30 min. The mixture was cooled to 0° C. (ice water) and a solution of N-methoxy-6, N-dimethyl-nicotinamide (72 mg, 0.4 mmol) in 1 mL of THF was added. The mixture was stirred at room temperature for 3 hours, quenched with 1M HCl and neutralized with 1M NaOH until pH was 9. The mixture was extracted with ethyl acetate, dried and concentrated. The residue was purified by flash column (silica gel, 50% ethyl acetate in hexane) to afford 36 mg of 4-chloro-N-[5-chloro-2-(6-methyl-pyridine-3-carbonyl)-pyridin-3-yl]-N-methoxymethyl-3-trifluoromethyl-benzenesulfonamide as an off white solid. MS: (M+H)/z=534.0.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08093247B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-24e53151dda7446581e9d57fc2bd9779
출처 메모uspto-grants-2012_01