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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1186617생성일: 2026년 10월 25일

Cyclohexene → N-[5-(3,5-difluorobenzyl)-1H-indazol-3-yl]-4-amino-2-[tetrahydro-2H-pyran-4-yl(trifluoroacetyl)amino]benzamide

https://huagongshe.com/reaction/1186617

반응식

참여 물질

역할이름HCID투입량
반응물CyclohexeneHCID 8079—
반응물N-[5-(3,5-difluorobenzyl)-1H-indazol-3-yl]-4-nitro-2-[tetrahydro-2H-pyran-4-yl(trifluoroacetyl)amino]benzamideHCID 86647627—
촉매PalladiumHCID 23938—
용매1,4-DioxaneHCID 31275—
생성물N-[5-(3,5-difluorobenzyl)-1H-indazol-3-yl]-4-amino-2-[tetrahydro-2H-pyran-4-yl(trifluoroacetyl)amino]benzamideHCID 8664762882%

반응 조건

온도100 °C

반응 단계

A mixture of N-[5-(3,5-difluorobenzyl)-1H-indazol-3-yl]-4-nitro-2-[tetrahydro-2H-pyran-4-yl(trifluoroacetyl)amino]benzamide (3.86 g, 6.4 mmol), cyclohexene (10 mL), dioxane (70 mL) and 10% Pd/C (0.42 g) was stirred at 100° C. for 4 hours. The reaction mixture was filtered over a celite pad washing thoroughly with THF and MeOH. After evaporation of the organic phase, purification of the crude by chromatography over silica gel (DCM/EtOH 9/1) gave 2.75 g of title compound (82% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08673893B2
출처 데이터셋uspto-grants-2014_03
ORD IDord-7a723b0d88d641e5b580aa43d501302d
출처 메모uspto-grants-2014_03