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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 71278생성일: 2026년 10월 24일

2,4-Dichloro-5-fluoropyrimidine → N4-[4-(N-benzylpiperazino)phenyl]-2-chloro-5-fluoro-4-pyrimidineamine

https://huagongshe.com/ko/reaction/71278

반응식

참여 물질

역할이름HCID투입량
반응물2,4-Dichloro-5-fluoropyrimidineHCID 250705—
반응물4-(4-Benzylpiperazin-1-yl)anilineHCID 737259—
생성물N4-[4-(N-benzylpiperazino)phenyl]-2-chloro-5-fluoro-4-pyrimidineamineHCID 86591122—

반응 단계

In like manner to the preparation of 2-chloro-N4-(3,4-ethylenedioxyphenyl)-5-fluoro-4-pyrimidineamine, 4-(N-benzylpiperazino)aniline and 2,4-dichloro-5-fluoropyrimidine gave N4-[4-(N-benzylpiperazino)phenyl]-2-chloro-5-fluoro-4-pyrimidineamine. 1H NMR (CDCl3): δ 2.81 (m, 4 H), 3.37 (m, 6 H), 6.85 (br, 1 H), 6.93 (d, J=9.0 Hz, 2H), 7.40 (m, 5H), 7.50 (d, J=9.3 Hz, 2 H), 8.02 (d, J=2.7 Hz, 1 H); LCMS: ret. time: 20.56 min, purity: 97.75%; MS (m/e): 398.00 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822685B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-0c63a753fbe64c698a8df89f8a20c707
출처 메모uspto-grants-2014_09