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HRID 279337作成日:2026年10月25日

Acetonitrile → 4-[[N-(2-amino-5-chlorobenzoyl) glycyl]aminomethyl]-1-[4-(trifluoromethylthio)benzyl]piperidine

https://huagongshe.com/reaction/279337

反応式

関与物質

役割名称HCID仕込み量
反応物AcetonitrileHCID 6342—
反応物4-(Trifluoromethylthio)benzyl bromideHCID 2777882—
反応物4-[{N-(2-amino5-chlorobenzoyl)glycyl}aminomethyl]piperidineHCID 18426216—
溶媒ChloroformHCID 6212—
生成物4-[[N-(2-amino-5-chlorobenzoyl) glycyl]aminomethyl]-1-[4-(trifluoromethylthio)benzyl]piperidineHCID 1842624485%

反応条件

温度60 °C

反応手順

A mixture of 4-[{N-(2-amino5-chlorobenzoyl)glycyl}aminomethyl]piperidine (16.2 mg, 0.050 mmol), 4-(trifluoromethylthio)benzyl bromide (20.3 mg, 0.075 mmol), piperidinomethylpolystyrene (60 mg), acetonitrile (1.0 mL) and chloroform (0.50 mL) was stirred at 60° C. for 15 h. The reaction mixture was cooled, loaded onto Varian™ SCX column and washed with CH3OH (15 mL). Product was eluted using 2 N NH3 in CH3OH (5 mL) and concentrated to afford 4-[{N-(2-amino-5-chlorobenzoyl)glycyl}aminomethyl]-1-{4-(trifluoromethylthio)benzyl}piperidine (Compound No.1616) (21.9 mg, 85%): The purity was determined by RPLC/MS (96%); ESI/MS m/e 545.2 (M++H, C23H26ClF3N4O2S).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06362177B1
出典データセットuspto-grants-2002_03
ORD IDord-f99304bb7cbf4d8c80c87a0861c30f2d
出典メモuspto-grants-2002_03