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HRID 2109930作成日:2026年10月25日

Potassium Carbonate → 3-tert-butyl-1-(2-methoxy-6-methylphenyl)-4-methyl-1H-pyrazol-5-amine

https://huagongshe.com/reaction/2109930

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4-bromo-3-tert-butyl-1-(2-methoxy-6-methylphenyl)-1H-pyrazol-5-amineHCID 57635877—
反応物CID 177697481HCID 177697481—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物3-tert-butyl-1-(2-methoxy-6-methylphenyl)-4-methyl-1H-pyrazol-5-amineHCID 5763582381%

反応条件

温度155 °C

反応手順

To a solution of 4-bromo-3-tert-butyl-1-(2-methoxy-6-methylphenyl)-1H-pyrazol-5-amine (2.6 g, 7.68 mmol) in DMF (15 mL) was added methylboroxine (6.66 mL, 46.08 mmol), [1,1′-bis(diphenylphosphino)-butane]palladium (II) dichloride (481.97 mg, 0.80 mmol), and potassium carbonate (3.3 g, 23.04 mmol). The reaction mixture was stirred for 18 h at 155° C. The reaction was diluted with water (100 mL) and extracted with EtOAc (3×25 mL). The combined organic extracts were washed with brine, dried (Na2SO4), and concentrated under reduced pressure. The residue was purified by silica gel chromatography using 90% hexane/EtOAc, to afford the product (1.7 g, 77%) as a pure white solid. 1H NMR (300 MHz, DMSO-d6) δ 1.24 (s, 9H), 1.96 (s, 3H), 1.99 (s, 3H), 3.71 (s, 3H), 4.25 (s, 2H), 6.85 (d, 1H), 6.94 (d, 1H), 7.23-7.29 (m, 1H). ES-MS m/z 274.2 (MH+); HPLC RT (min.) 1.78.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07517878B2
出典データセットuspto-grants-2009_04
ORD IDord-85ef39d8436a47d4ae1d742bc37e4d7f
出典メモuspto-grants-2009_04