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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 279337생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/279337

반응식

참여 물질

역할이름HCID투입량
반응물AcetonitrileHCID 6342—
반응물4-(Trifluoromethylthio)benzyl bromideHCID 2777882—
반응물4-[{N-(2-amino5-chlorobenzoyl)glycyl}aminomethyl]piperidineHCID 18426216—
용매ChloroformHCID 6212—
생성물4-[[N-(2-amino-5-chlorobenzoyl) glycyl]aminomethyl]-1-[4-(trifluoromethylthio)benzyl]piperidineHCID 1842624485%

반응 조건

온도60 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06362177B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-f99304bb7cbf4d8c80c87a0861c30f2d
출처 메모uspto-grants-2002_03