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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 216134생성일: 2026년 10월 26일

Sodium Bicarbonate → [2-Methoxy-6-(3-methoxy-phenyl)-pyrimidin-4-yl]-[2-(4-methoxy-phenyl)-2-methyl-propyl]-amine

https://huagongshe.com/reaction/216134

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참여 물질

역할이름HCID투입량
반응물Sodium BicarbonateHCID 516892—
반응물2-(4-Methoxyphenyl)-2-methylpropan-1-amineHCID 3581364—
반응물4-Chloro-2-methoxy-6-(3-methoxy-phenyl)-pyrimidineHCID 57636038—
용매WaterHCID 962—
용매1-MethylpyrrolidineHCID 8454—
생성물[2-Methoxy-6-(3-methoxy-phenyl)-pyrimidin-4-yl]-[2-(4-methoxy-phenyl)-2-methyl-propyl]-amineHCID 1163258769.4%

반응 조건

온도175 °C

반응 단계

A mixture of 2-(4-methoxy-phenyl)-2-methyl-propylamine [172 mg, 0.96 mmol, Intermediate (35)], sodium bicarbonate (0.12 g), and 4-chloro-2-methoxy-6-(3-methoxy-phenyl)-pyrimidine [120 mg, 0.48 mmol, Intermediate (53)] in N-methylpyrrolidine (3 mL), is heated to 175° C. for 3 hours. The mixture is diluted with water, and extracted with ethyl acetate. The extracts are washed with water, dried over magnesium sulfate, filtered and concentrated. The residue is subjected to chromatography on silica gel eluting with 30% EtOAc in heptane to afford [2-methoxy-6-(3-methoxy-phenyl)-pyrimidin-4-yl]-[2-(4-methoxy-phenyl)-2-methyl-propyl]-amine [131 mg, 69%, Example 29]. LCMS: RT=2.73 minutes, MS: 394 (M+H). 1H NMR (300 MHz, CDCl3): □7.59 (1H, s), 7.51 (1H, d, J=7.8 Hz), 7.35-7.27 (3H, m), 6.96 (1H, dd, J=8.1, 2.4 Hz), 6.88 (2H, d, J=9 Hz), 6.31 (1H, s), 4.02 (3H, s), 3.86 (3H, s), 3.79 (3H, s), 3.62 (2H, brs), 1.4 (6H, s). IC50=792 nM

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08193183B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-be496aedbd9546e79392ec7703a70b03
출처 메모uspto-grants-2012_06