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HRID 735313作成日:2026年10月24日

Ammonia → (1S)-1-(2-{[6-(2,4-Difluorophenyl)-2-naphthyl]sulfonyl}phenyl)ethanol

https://huagongshe.com/ja/reaction/735313

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物1-(2-Bromophenyl)ethan-1-olHCID 6950331—
反応物HCID 68899091HCID 68899091—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
溶媒Dimethyl SulfoxideHCID 679—
生成物(1S)-1-(2-{[6-(2,4-Difluorophenyl)-2-naphthyl]sulfonyl}phenyl)ethanolHCID 6890113426.5%

反応条件

温度110 °C

反応手順

Sodium 6-(2,4-difluorophenyl)naphthalene-2-sulfinate (Step 3, 486 mg, 1.49 mmol), (1S)-1-(2-bromophenyl)ethanol (260 mg, 1.29 mmol) and copper(I) iodide (1.23 g, 6.46 mmol) were combined in dimethylsulfoxide (10 mL) and degassed. The reaction was heated to 110° C. for 2 hours. The cooled reaction mixture was poured into conc. ammonia solution and extracted with diethyl ether (x4). The combined organic layers were washed with brine, dried over MgSO4 and evaporated in vacuo. The residue was purified by flash column chromatography on silica, eluting with 5% then 10% diethyl ether/dichloromethane, followed by trituration with isohexane. A second column, eluting with 60% diethyl ether/isohexane, followed by trituration with isohexane, gave the title compound (145 mg). 1H NMR (500 MHz, CDCl3) δ 8.56 (1H, s), 8.17 (1H, d, J=7.9 Hz), 8.06-7.98 (3H, m), 7.79-7.76 (3H, m), 7.66 (1H, t, J=7.5 Hz), 7.54-7.48 (2H, m), 7.03-6.95 (2H, m), 5.65 (1H, q, J=6.2 Hz), 2.51 (1H, s), 1.35 (3H, d, J=6.3 Hz); m/z (ES+) 407 [(M-OH)+].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07592456B2
出典データセットuspto-grants-2009_09
ORD IDord-e30a3a2243824c7abfb49235fe7dd579
出典メモuspto-grants-2009_09