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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 226585생성일: 2026년 10월 27일

2,4-Dichloro-5-fluoropyrimidine → 2-chloro-N4-[2-(2-chloro-5-fluoropyrimidin-4-yl)-1,2,3,4-tetrahydroisoquinolin-7-yl]-5-fluoro-4-pyrimidineamine

https://huagongshe.com/reaction/226585

반응식

참여 물질

역할이름HCID투입량
반응물2,4-Dichloro-5-fluoropyrimidineHCID 250705—
반응물1,2,3,4-Tetrahydroisoquinolin-7-amineHCID 11586323—
생성물2-chloro-N4-[2-(2-chloro-5-fluoropyrimidin-4-yl)-1,2,3,4-tetrahydroisoquinolin-7-yl]-5-fluoro-4-pyrimidineamineHCID 22060957—

반응 단계

In a like manner to the preparation of N2,N4-bis(3-hydroxyphenyl)-5-fluoro-2,4-pyrimidinediamine, 2,4-dichloro-5-fluoropyrimidine and 7-amino-1,2,3,4-tetrahydroisoquinoline were reacted to provide 2-chloro-N4-[2-(2-chloro-5-fluoropyrimidin-4-yl)-1,2,3,4-tetrahydroisoquinolin-7-yl]-5-fluoro-4-pyrimidineamine. 1H NMR (CDCl3): δ 8.08 (d, 1H, J=3.0 Hz), 7.95 (d, 1H, J=6.0 Hz), 7.50–7.42 (m, 2H), 7.21 (d, 1H, J=8.4 Hz), 6.96–6.90 (m, 1H), 4.95 (s, 2H), 4.04 (t, 2H, J=5.7 Hz), 2.99 (t, 2H, J=5.7 Hz); 19F NMR (282 MHz, CDCl3): −42555, −44573; LCMS: purity: 98%; MS (m/e): 410(MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07557210B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-347a5ae07ed944beb4f9878c86bc14f5
출처 메모uspto-grants-2009_07