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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 76520생성일: 2026년 10월 24일

3-Aminobenzonitrile → N2,N4-bis(3-cyanophenyl)-5-fluoro-2,4-pyrimidinediamine

https://huagongshe.com/ko/reaction/76520

반응식

참여 물질

역할이름HCID투입량
반응물3-AminobenzonitrileHCID 16702—
반응물2,4-Dichloro-5-fluoropyrimidineHCID 250705—
반응물R-112HCID 9904854—
생성물N2,N4-bis(3-cyanophenyl)-5-fluoro-2,4-pyrimidinediamineHCID 2206075676%

반응 단계

In a manner analogous to the preparation of N2,N4-bis(3-hydroxyphenyl)-5-fluoro-2,4-pyrimidinediamine, 3-aminobenzonitrile (177 mg, 1.5 mmol) and 2,4-dichloro-5-fluoropyrimidine (50 mg, 0.3 mmol) gave N2,N4-bis(3-cyanophenyl)-5-fluoro-2,4-pyrimidinediamine (75 mg, 76%). 1H NMR (acetone-d6): δ 7.33 (dt, J=1.8, 7.8 Hz, 1H), 7.46-7.52 (m, 2H), 7.59 (t, J=7.8 Hz, 1H), 7.90 (ddd, J=0.9, 2.1 and 8.4 Hz, 1H), 8.09 (ddd, J=1.2, 2.4 and 8.4 Hz, 1H), 8.17 (d, J=3.3 Hz, 1H), 8.31 (m, 1H), 8.35 (t, J=2.1 Hz, 1H), 8.98 (br, 1H, NH), 9.02 (br, 1H, NH); 19F NMR (282 MHz, acetone-d6): δ−165.80; LCMS: 24.64 min.; purity: 98.02%; MS (m/e): 331.01 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08835430B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-f7f22e3e05a046b5bfc83bd8793e43db
출처 메모uspto-grants-2014_09