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HRID 77491作成日:2026年10月25日

Potassium Carbonate → N-(4-(difluoromethoxy)phenyl)-6-vinylpyridazin-3-amine

https://huagongshe.com/reaction/77491

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物2-Ethenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 5233012—
反応物6-chloro-N-(4-(difluoromethoxy)phenyl)pyridazin-3-amineHCID 43235448—
溶媒WaterHCID 962—
溶媒1,4-DioxaneHCID 31275—
生成物N-(4-(difluoromethoxy)phenyl)-6-vinylpyridazin-3-amineHCID 8667978561.9%

反応条件

温度80 °C

反応手順

To a solution of 6-chloro-N-(4-(difluoromethoxy)phenyl)pyridazin-3-amine (0.2 g, 0.736 mmol) in dioxane and water mixture were added vinylboronic acid pinacol ester (0.146 mL, 1.104 mmol), and K2CO3 (0.305 g, 2.209 mmol). The mixture was flushed for 15 min with nitrogen. PdCl2 (dppf)-CH2Cl2 adduct (0.060 g, 0.074 mmol) was then added and the reaction mixture heated at 80° C. for 18 h. The reaction mixture was filtered through a pad of celite, washed with ethyl acetate and purified by flash chromatography on silica gel using ethyl acetate in hexane to give N-(4-(difluoromethoxy)phenyl)-6-vinylpyridazin-3-amine as a white solid (0.12 g, 59%). 1HNMR 400 MHz, DMSO-d6: δ ppm 5.47 (d, J=1.20 Hz, 1H), 6.06 (dd, J=0.80, 23.80 Hz, 1H), 6.84-7.38 (m, 5H), 7.75-7.82 (m, 3H), 9.42 (s, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08841301B2
出典データセットuspto-grants-2014_09
ORD IDord-70a27a3b47514ec89815ce94e3d224e7
出典メモuspto-grants-2014_09