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HRID 535046作成日:2026年10月26日

Water → 1-benzyl 4-methyl (2S)-2-[benzyl((2S)-2-hydroxy-3-[(4-methylphenyl)sulfonyl]oxypropyl)amino]succinate

https://huagongshe.com/reaction/535046

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Sodium FluorideHCID 5235—
反応物Oxiranemethanol, 4-methylbenzenesulfonate, (S)-HCID 153296—
反応物TrimethylaluminumHCID 16682925—
反応物Acetone cardiceHCID 18522661—
反応物(S)-2-benzylamino-succinic acid 1-benzyl ester 4-methyl esterHCID 67303755—
溶媒TolueneHCID 1140—
溶媒DichloromethaneHCID 6344—
生成物1-benzyl 4-methyl (2S)-2-[benzyl((2S)-2-hydroxy-3-[(4-methylphenyl)sulfonyl]oxypropyl)amino]succinateHCID 8734866891.8%

反応条件

温度-78 °C

反応手順

To a solution of (2S)-(+)-glycidyl tosylate (23.0 g, 0.101 mol) in 500 mL of methylene chloride was added 2.00 M of trimethylaluminum in toluene (50.4 mL) at −78 Celsius, under an atmosphere of nitrogen. After stirred at −78 Celsius for 10 min, to the mixture was added a solution of (S)-2-benzylamino-succinic acid 1-benzyl ester 4-methyl ester (30.0 g, 0.0916 mol) in 150 mL of methylene chloride. The resulting reaction mixture was stirred at −78 Celsius for 30 min. The dry ice-acetone bath was changed to an ice-water bath to warm the mixture up to 0 Celsius. The mixture was stirred at 0 Celsius for 30 min. To the reaction mixture was added sodium fluoride (16.2 g, 0.385 mol) followed by water (10.4 mL, 0.577 mol) at 0 Celsius. The resulting suspension was rapidly stirred for 1 h at 0 Celsius and filtered through a short column of celite and the column was subsequently washed with 600 mL of methylene chloride. The combined filtrates were dried over sodium sulfate, concentrated to dry and purified by column purification (eluting with 0 to 20% EtOAc in hexane) to yield the titled compound (46.7 g, 91.7%). MS (ESI): (M+H)+=556.2.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08853243B2
出典データセットuspto-grants-2014_10
ORD IDord-2f6ffbcd435a4f7da3859880e24c9c1e
出典メモuspto-grants-2014_10