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HRID 2181918作成日:2026年10月27日

Triethylamine → N-[1-(2',5',5-Trifluoro-1,1'-biphenyl-2-yl)ethyl]-3-methoxybenzenesulfonamide

https://huagongshe.com/reaction/2181918

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物3-Methoxybenzenesulfonyl chlorideHCID 2737504—
反応物1-(2',5',5-Trifluoro-1,1'-biphenyl-2-yl)ethylamineHCID 22482279—
生成物N-[1-(2',5',5-Trifluoro-1,1'-biphenyl-2-yl)ethyl]-3-methoxybenzenesulfonamideHCID 22482389100%

反応手順

The title compound was prepared from 3-methoxybenzenesulfonyl chloride (153 mg, 0.74 mmol), 1-(-2′,5′,5-trifluoro-1,1′-biphenyl-2-yl)ethylamine (177 mg, 0.70 mmol), and triethylamine (147 uL, 1.1 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 (295 mg, 100%) 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-4f2e9c43accc4ec891d7b521905263d2
出典メモuspto-grants-2005_05