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HRID 1669962作成日:2026年10月26日

2,5-Dichloronitrobenzene → Escitalopram Oxalate

https://huagongshe.com/reaction/1669962

反応式

関与物質

役割名称HCID仕込み量
反応物2,5-DichloronitrobenzeneHCID 6977—
反応物Potassium CarbonateHCID 11430—
反応物Oxalic acid dihydrateHCID 61373—
反応物Citadiol, (S)-HCID 7472057—
溶媒AcetoneHCID 180—
溶媒Dimethyl SulfoxideHCID 679—
溶媒WaterHCID 962—
生成物Escitalopram OxalateHCID 146571—

反応条件

温度100 °C

反応手順

To a solution of 6.0 gm of (S)-(−)-4-[4-(dimethylamino)-1-(4-fluorophenyl)-1-hydroxy-1-butyl]-3-(hydroxymethyl)benzonitrile in 30 ml of DMSO at room temperature was added 7.3 gm of anhydrous K2CO3 and 4.04 gm of 2,5-dichloronitrobenzene was added to the above reaction mixture at room temperature and stirred at 100° C. for 15.0 hours. To the above reaction mixture, 120 ml of water was added, and extracted with toluene. The toluene layer was washed with water and 5% sodium hydroxide solution and after acid base treatment yielded an oily product. The oil was dissolved in 16 ml of acetone at 30° C. and 1.9 gm of oxalic acid dihydrate in 8 ml of acetone was added to it, stirred, cooled, filtered and dried at 60° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07989645B2
出典データセットuspto-grants-2011_08
ORD IDord-7a213609d29543c4811ac4e2a999e69c
出典メモuspto-grants-2011_08