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HRID 279306作成日:2026年10月26日

Methanol → 1-(4-chlorobenzyl)-4-[[N-(3,5-bis(trifluoromethyl)benzoyl)glycyl]aminomethyl]piperidine

https://huagongshe.com/reaction/279306

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物3,5-Bis(trifluoromethyl)benzoyl chlorideHCID 101856—
反応物1-(4-Chlorobenzyl)-4-((glycylamino)methyl}piperidineHCID 18426155—
溶媒ChloroformHCID 6212—
溶媒DichloromethaneHCID 6344—
生成物1-(4-chlorobenzyl)-4-[[N-(3,5-bis(trifluoromethyl)benzoyl)glycyl]aminomethyl]piperidineHCID 18426201—

反応手順

A solution of 3,5-bis(trifluoromethyl)benzoyl chloride (0.058 mmol) in dichloromethane (1 mL) was added to a mixture of 1-{4-chlorobenzyl)-4-((glycylamino)methyl}piperidine (0.050 mmol) and piperidinomethylpolystyrene (58 mg) in chloroform (0.2 mL) and dichloromethane (0.75 mL). After the reaction mixture was stirred at room temperature for 2 h, methanol (1.0 mL) was added and the mixture was stirred at room temperature for 30 min. The reaction mixture was loaded onto Varian™ SCX column, and washed with CH3OH (16 mL). Product was eluted off using 2 N NH3, in CH3OH (6 mL) and concentrated to afford 1-(4-chlorobenzyl)-4-[{N-(3,5-bis(trifluoromethyl)benzoyl)glycyl}aminomethyl]piperidine (Compound No. 1213) (24.0 mg, 90%): The purity was determined by RPLC/MS (100%); ESI/MS m/e 536.2 (M++H, C24H24ClF6N3O2).

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-269902fa29484300a9c374fc4b7af816
出典メモuspto-grants-2002_03