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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 494158생성일: 2026년 10월 24일

Hydrazine → N-[4-[(1E)-3-amino-1-propenyl]phenyl]-4'-(trifluoromethyl)-[1,1'-biphenyl]-2-carboxamide

https://huagongshe.com/ko/reaction/494158

반응식

참여 물질

역할이름HCID투입량
반응물HydrazineHCID 9321—
반응물N-[4-[(1E)-3-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-1-propenyl]phenyl]-4'-(trifluoromethyl)-[1,1'-biphenyl]-2-carboxamideHCID 21895288—
용매EthanolHCID 702—
생성물N-[4-[(1E)-3-amino-1-propenyl]phenyl]-4'-(trifluoromethyl)-[1,1'-biphenyl]-2-carboxamideHCID 21895285126.1%

반응 단계

A mixture of intermediate (2) (0.005 mol) and an aqueous hydrazine solution (0.005 mol) in ethanol (30 ml) was stirred and refluxed for 2 hours. The precipitate was filtered and washed with ethanol. Water was added. The suspension was basified with NaOH and filtered over celite. Celite was washed with ethyl acetate. The filtrate was extracted with ethyl acetate and washed with K2CO3, then with NaCl. The organic layer was separated, dried, filtered, and the solvent was evaporated. The residue was crystallized from ACN. The precipitate was filtered off and dried, yielding 2.5 g of N-[4-[(1E)-3-amino-1-propenyl]phenyl]-4′-(trifluoromethyl)-[1,1′-biphenyl]-2-carboxamide (intermediate 3; mp. 190° C.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07538124B2
출처 데이터셋uspto-grants-2009_05
ORD IDord-6e274d00fdbe43af8fdd80d9bd1fa93e
출처 메모uspto-grants-2009_05