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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 226898생성일: 2026년 10월 24일

Diisopropylethylamine → 5-fluoro-N4-(3-methylaminocarbonyl-4-methoxyphenyl)-N2-methyl-2,4-pyrimidinediamine

https://huagongshe.com/ko/reaction/226898

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참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물Methylamine hydrochlorideHCID 6364545—
반응물2-chloro-5-fluoro-N4-(3-methyloxycarbonyl-4-methoxyphenyl)-4-pyrimidineamineHCID 22060802—
용매MethanolHCID 887—
용매WaterHCID 962—
생성물5-fluoro-N4-(3-methylaminocarbonyl-4-methoxyphenyl)-N2-methyl-2,4-pyrimidinediamineHCID 22060470—

반응 조건

온도100 °C

반응 단계

A mixture of 2-chloro-5-fluoro-N4-(3-methyloxycarbonyl-4-methoxyphenyl)-4-pyrimidineamine (0.15 g, 0.4 mmol), methylamine hydrochloride (0.324 g, 48 mmol) and diisopropylethylamine (0.84 mL, 48 mmol) in MeOH (2 mL) was heated in a sealed tube at 100° C. for 24 h (followed by TLC). The reaction was cooled to room temperature and diluted with H2O (20 mL). The solid was filtered, washed with H2O and dried to obtain 5-fluoro-N4-(3-methylaminocarbonyl-4-methoxyphenyl)-N2-methyl-2,4-pyrimidinediamine R940304. 1H NMR (DMSO-d6): δ 10.65 (1H, s), 8.48 (1H, s), 8.29 (2H, m), 7.93 (1H, m), 7.28 (1H, d, J=9 Hz), 4.00 (3H, s), 2.94 (3H, s), 2.90 (3H, d, J=4.5 Hz); purity: 90%; MS (m/e): 306 (MH+);

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07557210B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-4d14d4a28e47488eae698c690f20a51a
출처 메모uspto-grants-2009_07