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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 513285생성일: 2026년 10월 24일

Trifluoroacetic acid → 4-(1-Phenylcyclopropylamino)-6-(3-(piperazin-1-yl)phenylamino)nicotinamide

https://huagongshe.com/ko/reaction/513285

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물Cesium carbonateHCID 10796—
반응물Binap, (A+-)-HCID 634876—
반응물tert-Butyl 4-(3-aminophenyl)piperazine-1-carboxylateHCID 22330182—
반응물6-Chloro-4-(1-phenylcyclopropylamino)nicotinamideHCID 86664541—
촉매palladium(II) acetateHCID 167845—
용매DichloromethaneHCID 6344—
용매1,4-DioxaneHCID 31275—
생성물4-(1-Phenylcyclopropylamino)-6-(3-(piperazin-1-yl)phenylamino)nicotinamideHCID 56968704—

반응 조건

온도80 °C

반응 단계

To a mixture of 6-chloro-4-(1-phenylcyclopropylamino)nicotinamide (150 mg, 0.522 mmol) in p-Dioxane (4.5 mL) was added tert-butyl 4-(3-aminophenyl)piperazine-1-carboxylate (174 mg, 0.626 mmol), Pd(OAc)2 (23 mg, 0.104 mmol), BINAP (65 mg, 0.104 mmol) and Cs2CO3 (510 mg, 1.566 mmol). After stirred at 80° C. for 15 h, it was concentrated to give crude residue, which was then treated with TFA in DCM, 30 min later, the solution was concentrated, the residue was purified by preparative HPLC to give 4-(1-phenylcyclopropylamino)-6-(3-(piperazin-1-yl)phenylamino)nicotinamide. MS found for C25H28N6O as (M+H)+ 429.4. UV: λ=254.6 nm. 1H NMR: (CD3OD) δ 8.17 (s, 1H), 7.31-7.20 (m, 4H), 7.13 (m, 2H), 6.95 (dd, J=8.0, 2.0 Hz, 1H), 6.79 (t, J=2.0 Hz, 1H), 6.60 (dd, J=7.2, 2.0 Hz, 1H), 6.12 (s, 1H), 3.34 (m, 8H), 1.36 (m, 4H) ppm.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09102625B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-1a1cca8c149e4bdda16d8f9adfe98a25
출처 메모uspto-grants-2015_08