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HRID 2355781作成日:2026年10月27日

Pyridine → E 7820

https://huagongshe.com/reaction/2355781

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物3-Cyanobenzene-1-sulfonyl chlorideHCID 2801360—
反応物7-amino-4-methyl-1H-indole-3-carbonitrileHCID 11715247—
溶媒TetrahydrofuranHCID 8028—
生成物E 7820HCID 19697047.4%

反応手順

To a solution of 7-amino-3-cyano-4-methyl-1H-indole (10 g, 58.4 mmol) in tetrahydrofuran (200 ml) were added pyridine (20 ml) and 3-cyanobenzenesulfonyl chloride (12.5 g), followed by stirring at room temperature for 3.5 hours. After further adding 2N hydrochloric acid (100 ml), extraction was performed with ethyl acetate. The organic layer was washed with water (twice) and brine in that order, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=2:1-3:2). A mixed solvent of ethanol-hexane (1:2) was added thereto, and after sonication, the precipitate was collected by filtration and washed with a mixed solvent of ethanol-hexane (1:3). The mixture was dried overnight under reduced pressure to give the title compound (9.33 g, 27.7 mmol, 47% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07754894B2
出典データセットuspto-grants-2010_07
ORD IDord-a1376e18842647db882858a5a7bf7bda
出典メモuspto-grants-2010_07