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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 71290생성일: 2026년 10월 24일

Hydrochloric Acid → 2-chloro-N4-(4-n-butyloxyphenyl)-5-fluoro-4-pyrimidineamine

https://huagongshe.com/ko/reaction/71290

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sodium HydroxideHCID 14798—
반응물4-ButyloxyanilineHCID 20352—
반응물2,4-Dichloro-5-fluoropyrimidineHCID 250705—
용매Propan-2-one--water (1/1)HCID 18366337—
생성물2-chloro-N4-(4-n-butyloxyphenyl)-5-fluoro-4-pyrimidineamineHCID 2206107780%

반응 단계

To a solution of 2,4-dichloro-5-fluoropyrimidine (0.5 g, 3.0 mmol) and 4-n-butoxyaniline (0.49 g, 3 mmol) in acetone/H2O (1:9 mL) at room temperature was added concentrated HCl (0.1 mL). The mixture was heated at reflux for 1 h, cooled to room temperature, and made basic with 2 N NaOH (2 mL). The aqueous layer was extracted with EtOAc (2×50 mL) and the combined organic extracts were dried (Na2SO4), filtered, and concentrated in vacuo. The crude black solid was purified by chromatography (4:1 hexanes/EtOAc) to afford 2-chloro-N4-(4-n-butyloxyphenyl)-5-fluoro-4-pyrimidineamine (0.71 g, 80%) as a brown oil: 1H NMR (300 MHz, CDCl3) δ 8.01 (d, J=2.7 Hz, 1H), 7.51-7.46 (m, 2H), 6.95-6.89 (m, 2H), 6.83 (bs, 1H), 3.99-3.95 (t, J=6.5 Hz, 2H), 1.82-1.57 (m, 2H), 1.53-1.43 (m, 2H), 0.98 (t, J=7.2 Hz, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822685B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-3faa52b78a234f0ba03a2b883b9b403f
출처 메모uspto-grants-2014_09