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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2265983생성일: 2026년 10월 26일

1-Methylpiperazine → N-(3-Ethynyl-5-fluoro-4-methanesulfonylamino-benzyl)-3-[2-(4-methyl-piperazin-1-yl)-6-trifluoromethyl-pyridin-3-yl]-acrylamide

https://huagongshe.com/reaction/2265983

반응식

참여 물질

역할이름HCID투입량
반응물1-MethylpiperazineHCID 53167—
반응물3-(2-Chloro-6-trifluoromethyl-pyridin-3-yl)-N-(3-ethynyl-5-fluoro-4-methanesulfonylamino-benzyl)-acrylamideHCID 74382385—
생성물N-(3-Ethynyl-5-fluoro-4-methanesulfonylamino-benzyl)-3-[2-(4-methyl-piperazin-1-yl)-6-trifluoromethyl-pyridin-3-yl]-acrylamideHCID 7233564615%

반응 단계

3-(2-Chloro-6-trifluoromethyl-pyridin-3-yl)-N-(3-ethynyl-5-fluoro-4-methanesulfonylamino-benzyl)-acrylamide (70 mg, 0.057 mmol) was reacted with N-methylpiperazine (30 μl) as in example 46 to give the title compound (13 mg, 15%) after recrystallization with Hex/EtOAc.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07858621B2
출처 데이터셋uspto-grants-2010_12
ORD IDord-0fa91f094990421e9157804d00ca55ad
출처 메모uspto-grants-2010_12