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HRID 2181909作成日:2026年10月26日

4-Methoxybenzenesulfonyl chloride → N-[1-(2',4',5-Trifluoro-1,1'-biphenyl-2-yl)ethyl]-4-methoxybenzenesulfonamide

https://huagongshe.com/reaction/2181909

反応式

関与物質

役割名称HCID仕込み量
反応物4-Methoxybenzenesulfonyl chlorideHCID 7401—
反応物TriethylamineHCID 8471—
反応物1-(2',4',5-Trifluoro-1,1'-biphenyl-2-yl)ethylamineHCID 22482382—
生成物N-[1-(2',4',5-Trifluoro-1,1'-biphenyl-2-yl)ethyl]-4-methoxybenzenesulfonamideHCID 2248234070%

反応手順

The title compound was prepared from 4-methoxybenzenesulfonyl chloride (146 mg, 0.7 mmol), 1-(-2′,4′,5-trifluoro-1,1′-biphenyl-2-yl)ethylamine (169 mg, 0.67 mmol), and triethylamine (187 μL, 1.3 mmol) according to the procedure and in the same manner as described in Example 105, step c. The product was purified by preparative liquid chromatography on a Biotage® 40 Mi column of prepacked silica gel (90 g), eluting with a gradient of 30%-50% methyl tert-butyl ether in hexane (35 min), to afford the desired compound (197 mg, 70%) as a white solid;

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06894061B2
出典データセットuspto-grants-2005_05
ORD IDord-dfd8cad47b7245c2af27b0850ed039c6
出典メモuspto-grants-2005_05