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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 76533생성일: 2026년 10월 23일

2-Methyl-5-Nitroaniline → N2,N4-bis(2-methyl-5-nitrophenyl)-5-fluoro-2,4-pyrimidinediamine

https://huagongshe.com/ko/reaction/76533

반응식

참여 물질

역할이름HCID투입량
반응물2-Methyl-5-NitroanilineHCID 7444—
반응물2,4-Dichloro-5-fluoropyrimidineHCID 250705—
용매MethanolHCID 887—
용매WaterHCID 962—
생성물N2,N4-bis(2-methyl-5-nitrophenyl)-5-fluoro-2,4-pyrimidinediamineHCID 22060573—

반응 조건

온도70 °C

반응 단계

2,4-Dichloro-5-fluoropyrimidine (33 mg, 0.2 mmol) was dissolved in a mixture of MeOH (1 ml) and H2O (0.1 ml). 2-Methyl-5-nitroaniline (122 mg, 0.8 mmol) was added and the mixture was refluxed for 2 days (70° C. oil-bath temperature). The mixture was cooled to 22° C., concentrated to dryness under reduced pressure and subjected to column chromatography on silica gel (CHCl3-Acetone, 9:1) to give N2,N4-bis(2-methyl-5-nitrophenyl)-5-fluoro-2,4-pyrimidinediamine. 1H NMR (DMSO-d6+CD3OD): δ 8.31 (d, 1H, J=2.3 Hz), 8.20 (d, 1H, J=2.3 Hz), 8.06 (d, 1H, J=3.5 Hz), 7.91 (dd, 1H, J=2.3, 8.2 Hz), 7.65 (dd, 1H, J=2.9, 8.8 Hz), 7.41 (m, 1H), 7.28 (d, 1H, J=8.2 Hz), 2.28 (s, 3H), 2.24 (s, 3H); LCMS purity: 87.4%; MS (m/e): 399.20 (M+, 100).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08835430B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-c984e48e9d8541d780e255e305477f21
출처 메모uspto-grants-2014_09