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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1692990생성일: 2026년 10월 26일

N,N-Dimethylaniline → 4-chloro-N-(3-chlorophenyl)pyrimidin-2-amine

https://huagongshe.com/reaction/1692990

반응식

참여 물질

역할이름HCID투입량
반응물N,N-DimethylanilineHCID 949—
반응물Sodium HydroxideHCID 14798—
반응물Phosphorus oxychlorideHCID 24813—
반응물2-(3-chlorophenylamino)pyrimidin-4(3H)-oneHCID 1639233—
용매TolueneHCID 1140—
생성물4-chloro-N-(3-chlorophenyl)pyrimidin-2-amineHCID 5902824361%

반응 단계

To 2-(3-chlorophenylamino)pyrimidin-4(3H)-one, 2, (3.00 g, 13.5 mmol) in toluene (30 mL) is added N,N-dimethyl-aniline (3.57 mL, 28.4 mmol) and phosphorus oxychloride (1.24 mL, 13.5 mmol). The resulting mixture is heated to reflux for 15 minutes, cooled to room temperature and neutralized to pH 7 with 1M NaOH (aqueous). The organic layer is extracted with EtOAc (3×250 mL). The combined organic layers are dried (MgSO4) and concentrated in vacuo. The residue is purified over silica (5% EtOAc in hexanes) to afford 2.0 g (61% yield) of the desired compound. 1H NMR (DMSO-d6, 300 MHz): δ 7.06-7.04 (m, 2H), 7.34 (t, J=8.1, 1H), 7.65-7.61 (m, 1H), 7.93 (m, 1H), 8.50 (d, J=5.1 Hz, 1H), 10.26 (s, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08158641B2
출처 데이터셋uspto-grants-2012_04
ORD IDord-a161c0b9f7964422aeaae489c9b6d890
출처 메모uspto-grants-2012_04