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HRID 58072作成日:2026年10月25日

Sodium Carbonate → 4(2,4-dimethoxypyrimidin-5-yl)-6-(trifluoromethyl)-1H-indazole

https://huagongshe.com/reaction/58072

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5-Bromo-2,4-dimethoxypyrimidineHCID 255719—
反応物4-(Tetramethyl-1,3,2-dioxaborolan-2-yl)-6-(trifluoromethyl)-1H-indazoleHCID 89782806—
触媒Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
溶媒1,4-DioxaneHCID 31275—
生成物Trifluoroacetic acidHCID 6422—
生成物4(2,4-dimethoxypyrimidin-5-yl)-6-(trifluoromethyl)-1H-indazoleHCID 8978317745.2%

反応条件

温度130 °C

反応手順

4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-6-(trifluoromethyl)-1H-indazole (35 mg, 0.112 mmol), 5-bromo-2,4-dimethoxypyrimidine (24.56 mg, 0.112 mmol), and PdCl2(dppf) (8.21 mg, 0.011 mmol) were dispersed in dioxane (1.5 mL). To the resulting slurry was added 2N aqueous sodium carbonate (0.112 mL, 0.224 mmol). The mixture was purged with nitrogen, heated in a microwave reactor at 130° C. for 50 minutes, and then filtered through a microfiltration frit. Dioxane was stripped with nitrogen. The resulting residue was taken up in DMSO and methanol (1:1) and was purified via preparative HPLC, eluting with a gradient of ACN (containing 0.035% TFA) in H2O (containing 0.05% TFA). The purified fractions were collected to give a TFA salt of the title compound (8.2 mg, 23%). ESI-MS m/z [M+H]+ calc'd for C14H11F3N4O2, 325.1. found 325.2.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09434743B2
出典データセットuspto-grants-2016_09
ORD IDord-c1a4f9d86256414cb555e8b9c9efc9c1
出典メモuspto-grants-2016_09