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HRID 890253作成日:2026年10月26日

4-Toluenesulfonyl chloride → (2RS,5SR)-5-(4-Fluoro-phenyl)-1-(toluene-4-sulfonyl)-pyrrolidine-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/890253

反応式

関与物質

役割名称HCID仕込み量
反応物4-Toluenesulfonyl chlorideHCID 7397—
反応物TriethylamineHCID 8471—
反応物methyl (2RS,5SR)-5-(4-fluoro-phenyl)-pyrrolidine-2-carboxylateHCID 67257147—
溶媒DichloromethaneHCID 6344—
生成物(2RS,5SR)-5-(4-Fluoro-phenyl)-1-(toluene-4-sulfonyl)-pyrrolidine-2-carboxylic acid methyl esterHCID 69596768—

反応手順

To a stirred solution of methyl (2RS,5SR)-5-(4-fluoro-phenyl)-pyrrolidine-2-carboxylate (2.27 g, 10.2 mmol) and triethylamine (2.13 ml, 15.3 mmol) in dichloromethane (60 ml) was added at 0° C. toluene-4-sulfonyl chloride (2.32 g, 12.2 mmol). The mixture was stirred at RT for 16 h, evaporated, dissolved in water (50 ml) and extracted with dichloromethane (2×40 ml). The combined organic layers were washed with water (40 ml), brine (40 ml), dried (MgSO4) and evaporated. The crude product was purified by crystallization from diethyl ether/hexane to give the title compound, off-white solid, m.p. 91° C. and MS: m/e=378.3 (M+H+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06995182B2
出典データセットuspto-grants-2006_02
ORD IDord-7b718a8cb6ec46f0aee5d6b190df76e3
出典メモuspto-grants-2006_02