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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 606956생성일: 2026년 10월 25일

Methanesulfonyl chloride → N-[5-(5-Cyanopyridin-3-ylethynyl)-2-fluorophenyl]-methanesulfonamide

https://huagongshe.com/reaction/606956

반응식

참여 물질

역할이름HCID투입량
반응물Methanesulfonyl chlorideHCID 31297—
반응물5-(3-Amino-4-fluorophenylethynyl)-nicotinonitrileHCID 67047822—
용매WaterHCID 962—
용매PyridineHCID 1049—
용매TetrahydrofuranHCID 8028—
생성물N-[5-(5-Cyanopyridin-3-ylethynyl)-2-fluorophenyl]-methanesulfonamideHCID 6704758220%

반응 단계

Dissolve 5-(3-amino-4-fluorophenylethynyl)-nicotinonitrile, (prepared as described in EXAMPLE 160), (0.2 g, 0.8 mmol) in anhydrous pyridine. Add a solution of methanesulfonyl chloride (0.1 g, 0.88 mmol) in tetrahydrofuran to the reaction and stir overnight at room temperature. Concentrate and dissolve the crude reaction in ethyl acetate and water. Wash the organic layer with water, an aqueous saturated solution of sodium chloride, dry (potassium carbonate), filter, concentrate and purify (silica gel chromatography, eluting with 95:5 to 80:20 dichloromethane:ethyl acetate), to give the title compound as a tan solid (50 mg, 20%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07915424B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-e162a1bfde0440e4a4d47b5a19036340
출처 메모uspto-grants-2011_03