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HRID 1036944作成日:2026年10月27日

Pyridine → N-[3-(4,4-dimethyl-6-trifluoromethyl-1,2,3,4-tetrahydro-quinolin-2-yl)-phenyl]-2-fluoro-benzenesulfonamide

https://huagongshe.com/reaction/1036944

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物2-Fluorobenzenesulphonyl chlorideHCID 137761—
反応物3-(4,4-Dimethyl-6-trifluoromethyl-1,2,3,4-tetrahydro-quinolin-2-yl)-phenylamineHCID 67291615—
溶媒DichloromethaneHCID 6344—
生成物N-[3-(4,4-dimethyl-6-trifluoromethyl-1,2,3,4-tetrahydro-quinolin-2-yl)-phenyl]-2-fluoro-benzenesulfonamideHCID 5696612965.4%

反応手順

To a stirred solution of 3-(4,4-dimethyl-6-trifluoromethyl-1,2,3,4-tetrahydro-quinolin-2-yl)-phenylamine (100 mg, 0.31 mmol) in pyridine (49 mg, 0.62 mmol) and dichloromethane (1.5 mL) at 0° C. was added dropwise a solution of 2-fluoro-benzenesulfonyl chloride (73 mg, 0.37 mmol) in dichloromethane (0.5 mL). The mixture was stirred at room temperature overnight. The mixture was quenched with water (5 mL) and extracted with dichloromethane (5 mL×2). The combined organic layers were dried over anhydrous sodium sulfate and evaporated. The residue was purified by column chromatography on silica gel to afford N-[3-(4,4-dimethyl-6-trifluoromethyl-1,2,3,4-tetrahydro-quinolin-2-yl)-phenyl]-2-fluoro-benzenesulfonamide (97 mg, 65.1%) as a white solid. MS (ESI+APCI) M+1=479.1.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08546427B2
出典データセットuspto-grants-2013_10
ORD IDord-9eb6e1e722654da8bcb6813e322fdc2f
出典メモuspto-grants-2013_10