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HRID 606957作成日:2026年10月25日

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

https://huagongshe.com/reaction/606957

反応式

関与物質

役割名称HCID仕込み量
反応物Methanesulfonyl chlorideHCID 31297—
反応物5-(3-Amino-4-fluorophenylethynyl)-nicotinonitrileHCID 67047822—
溶媒WaterHCID 962—
溶媒PyridineHCID 1049—
溶媒TetrahydrofuranHCID 8028—
生成物N-[5-(5-Cyanopyridin-3-ylethynyl)-2-fluorophenyl]-N-methanesulfonyl-methanesulfonamideHCID 6704770936.2%

反応条件

温度50 °C

反応手順

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 (0.2 g, 1.9 mmol) in tetrahydrofuran to the reaction and heat at 50° C. for 16 h. 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 100:0 to 80:20 dichloromethane:ethyl acetate), to give the title compound as a white solid (114 mg, 36%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07915424B2
出典データセットuspto-grants-2011_03
ORD IDord-094567534f3147359f544421396bb3f5
出典メモuspto-grants-2011_03