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HRID 901608作成日:2026年10月24日

Phosphate → N-Cyclohexyl-3-(hydroxymethyl)-N-{[2-(trimethylsilyl)ethoxy]methyl}benzenesulfonamide

https://huagongshe.com/ja/reaction/901608

反応式

関与物質

役割名称HCID仕込み量
反応物PhosphateHCID 1061—
反応物Sodium hydrideHCID 24758—
反応物2-Chloromethyl 2-(trimethylsilyl)ethyl etherHCID 2724271—
反応物N-Cyclohexyl-3-(hydroxymethyl)benzenesulfonamideHCID 65751619—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物N-Cyclohexyl-3-(hydroxymethyl)-N-{[2-(trimethylsilyl)ethoxy]methyl}benzenesulfonamideHCID 66845530—

反応手順

A solution of N-cyclohexyl-3-(hydroxymethyl)benzenesulfonamide (1.744 g) in DMF (30 ml) under nitrogen was treated with sodium hydride (60% dispersion in mineral oil, 311 mg) and the mixture stirred at 20° for 0.5 h. 2-(Trimethylsilyl)ethoxymethyl chloride (1.15 ml) was added and the mixture was stirred for a further 2 h at 20°. Phosphate buffer solution (pH 6.5, 50 ml) and water (50 ml) were added and the mixture was extracted with EtOAc (2×50 ml). The combined extracts were washed with water (2×100 ml) and dried (Na2SO4). Solvent evaporation in vacuo gave a residue which was purified by flash chromatography on silica gel. Elution with EtOAc-PE (3:7) gave the title compound (1.917 g). LCMS RT=3.83 min, ES+ve 417 (MNH4)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07361787B2
出典データセットuspto-grants-2008_04
ORD IDord-b01da7e9147343698d6173e401ab4c1a
出典メモuspto-grants-2008_04