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HRID 28528作成日:2026年10月24日

Sodium Carbonate → 6-(5-Chloro-2-methoxy-phenyl)-N*4*-p-tolyl-pyrimidine-2,4-diamine

https://huagongshe.com/ja/reaction/28528

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium CarbonateHCID 10340—
反応物TriphenylphosphineHCID 11776—
反応物6-Chloro-n4-(4-methylphenyl)pyrimidine-2,4-diamineHCID 238748—
反応物5-Chloro-2-methoxyphenylboronic acidHCID 2735751—
触媒palladium(II) acetateHCID 167845—
溶媒WaterHCID 962—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物6-(5-Chloro-2-methoxy-phenyl)-N*4*-p-tolyl-pyrimidine-2,4-diamineHCID 1131383186%

反応条件

温度92.5 °C

反応手順

To a mixture of 6-chloro-N*4*-p-tolyl-pyrimidine-2,4-diamine (2.8 g, 11.9 mmol), 5-chloro-2-methoxy-phenyl boronic acid (3.96 g, 21.5 mmol), palladium (II) acetate (0.2 g, 0.9 mmol) and triphenylphosphine (0.47 g, 1.8 mmol) was added a solution of sodium carbonate (6.36 g, 60 mmol) in water (20 ml) followed by glyme (100 ml). The mixture was stirred under an argon atmosphere at 90-95° C. for 18 hours. Filtration and concentration of the filtrate yielded a residue which was purified by flash chromatography on silica gel eluting with ethyl acetate-hexane (1:3) to provide the title compound (3.48 g, 86% yield) as a white powder. 1H NMR (DMSO-d6) δ 2.27 (s, 3H, CH3), 3.88 (s, 3H, CH3), 6.27 (s, 2H, NH2), 6.72 (s, 1H, Ar), 7.10 (d, 2H, J=8.3 Hz, Ar), 7.16 (d, 1H, J=8.9 Hz, Ar), 7.44 (dd, 1H, J=8.9 Hz, J=2.8 Hz, Ar), 7.63 (d, 2H, J-8.3 Hz, Ar), 7.92 (d, 1H, J=2.8 Hz, Ar), 9.10 (s, 1H, NH).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07419984B2
出典データセットuspto-grants-2008_09
ORD IDord-686c3494ee2b4f5ab7659115bd34192e
出典メモuspto-grants-2008_09