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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 279306생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/279306

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물3,5-Bis(trifluoromethyl)benzoyl chlorideHCID 101856—
반응물1-(4-Chlorobenzyl)-4-((glycylamino)methyl}piperidineHCID 18426155—
용매ChloroformHCID 6212—
용매DichloromethaneHCID 6344—
생성물1-(4-chlorobenzyl)-4-[[N-(3,5-bis(trifluoromethyl)benzoyl)glycyl]aminomethyl]piperidineHCID 18426201—

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06362177B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-269902fa29484300a9c374fc4b7af816
출처 메모uspto-grants-2002_03