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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 490861생성일: 2026년 10월 26일

4-(4-Benzylpiperazin-1-yl)aniline → N-[4-[4-(phenylmethyl)-1-piperazinyl]phenyl]-4'-(trifluoro-methyl)-[1,1'-biphenyl]-2-carboxamide

https://huagongshe.com/reaction/490861

반응식

참여 물질

역할이름HCID투입량
반응물4-(4-Benzylpiperazin-1-yl)anilineHCID 737259—
반응물4'-(Trifluoromethyl)-[1,1'-biphenyl]-2-carbonyl chlorideHCID 11066000—
용매DichloromethaneHCID 6344—
용매TriethylamineHCID 8471—
생성물N-[4-[4-(phenylmethyl)-1-piperazinyl]phenyl]-4'-(trifluoro-methyl)-[1,1'-biphenyl]-2-carboxamideHCID 22499401104.6%

반응 단계

A mixture of 4′-(trifluoromethyl)-[1,1′-biphenyl]-2-carbonyl chloride (0.185 mole) in DCM (1500 ml) and triethylamine (50 ml) was stirred on an ice-bath for 5 minutes. 4-[4-(Phenylmethyl)-1-piperazinyl]-benzenamine (0.37 mole) in DCM (500 ml) was added dropwise. The mixture was stirred for 3 hours. The organic layer was separated, washed with water, dried, filtered and the solvent was evaporated. The residue was triturated in DIPE. The precipitate was filtered off and dried, yielding 99.8 g of N-[4-[4-(phenylmethyl)-1-piperazinyl]phenyl]-4′-(trifluoro-methyl)-[1,1′-biphenyl]-2-carboxamide (intermediate 5, melting point 180° C.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07528154B2
출처 데이터셋uspto-grants-2009_05
ORD IDord-a6448c7d7e01444fa25ed52f2d60ed39
출처 메모uspto-grants-2009_05