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HRID 1476410作成日:2026年10月26日

Sodium Bicarbonate → Methyl 1-isopropyl-6-(1H-pyrazol-4-yl)-1H-indazole-4-carboxylate

https://huagongshe.com/reaction/1476410

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium BicarbonateHCID 516892—
反応物4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazoleHCID 2774010—
反応物Methyl 6-bromo-1-isopropyl-1H-indazole-4-carboxylateHCID 67464993—
触媒HCID 178418807HCID 178418807—
溶媒WaterHCID 962—
溶媒1,4-DioxaneHCID 31275—
生成物Methyl 1-isopropyl-6-(1H-pyrazol-4-yl)-1H-indazole-4-carboxylateHCID 67467921—

反応手順

To a stirred solution of methyl 6-bromo-1-isopropyl-1H-indazole-4-carboxylate, 1 (0.8 g, 2.7 mmol) in 1,4-dioxane (20 mL) were added 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (0.576 g, 2.97 mmol) and NaHCO3 (0.567 g, 6.75 mmol) dissolved in water (8 mL). The reaction mixture was degassed with argon gas for 30 min. To the resulting mixture was added PdCl2(dppf)-CH2Cl2 adduct (0.110 g, 0.135 mmol) and the mixture heated at reflux for 3 h. The reaction mixture was diluted with water (30 mL) and extracted with ethyl acetate (100 mL). The organic layer was dried over anhydrous Na2SO4, filtered, and concentrated under reduced pressure to afford 800 mg of crude product. The crude compound was purified by silica gel chromatography (eluent: 5% MeOH/DCM) to the title compound as a pale liquid (375 mg, 47%). LCMS (ES−) m/z=283.11.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09018382B2
出典データセットuspto-grants-2015_04
ORD IDord-59d4437b9537419db01ea2e1b794eb59
出典メモuspto-grants-2015_04