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HRID 392458作成日:2026年10月25日

2,2,2-Trifluoroethanesulfonyl chloride → N-(3-(4-Cyanophenyl)phenyl)-N-(2,2,2-trifluoroethylsulfonyl)pyrid-3-ylmethylamine

https://huagongshe.com/reaction/392458

反応式

関与物質

役割名称HCID仕込み量
反応物2,2,2-Trifluoroethanesulfonyl chlorideHCID 74242—
反応物N-(3-(4-Cyanophenyl)phenyl)pyrid-3-ylmethylamineHCID 69880749—
溶媒Diethyl EtherHCID 3283—
溶媒DichloromethaneHCID 6344—
生成物N-(3-(4-Cyanophenyl)phenyl)-N-(2,2,2-trifluoroethylsulfonyl)pyrid-3-ylmethylamineHCID 23521688—

反応手順

A solution of N-(3-(4-cyanophenyl)phenyl)pyrid-3-ylmethylamine (255 mg, 0.894 mmol) in 8 ml dichloromethane/2 ml pyridine was treated with 2,2,2-trifluoroethylsulfonyl chloride in 3 portions of 171 mg (0.94 mmol) over 1 h at 45° C. The solution was cooled and diluted with 60 ml diethyl ether and washed successively with water and saturated sodium bicarbonate solution. The organics were separated, dried over sodium sulfate, filtered, and concentrated to an oil. The oil was purified by radial chromatography on a 2 micron silica plate eluting with 2 to 4% methanol/dichloromethane to afford the title compound. 1H NMR: 8.65 (bs,1H), 8.42 (bs,1H), 7.85 (m,1H), 7.75 (d,2H,J=8 Hz), 7.58 (d,2H,J=8 Hz), 7.30-7.55 (m,5H), 5.02 (s,2H), 3.78 (q,2H,J=8 Hz). MS calcd. 431.44; MS (M+1) 432.1.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06800651B2
出典データセットuspto-grants-2004_10
ORD IDord-23f10e7c6f7d4be9a58ebc3a85ef1c0e
出典メモuspto-grants-2004_10