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HRID 58075作成日:2026年10月25日

Sodium Bicarbonate → 4-(2-methoxypyrimidin-5-yl)-6-(trifluoromethyl)-1H-indazole

https://huagongshe.com/reaction/58075

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2-Methoxypyrimidine-5-boronic acidHCID 2736778—
反応物4-Bromo-6-(trifluoromethyl)-1H-indazoleHCID 24729232—
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-methoxypyrimidin-5-yl)-6-(trifluoromethyl)-1H-indazoleHCID 8978343339%

反応条件

温度140 °C

反応手順

A vial was charged with a mixture of 4-bromo-6-(trifluoromethyl)-1H-indazole (0.1 g, 0.377 mmol), (2-methoxypyrimidin-5-yl)boronic acid (0.076 g, 0.491 mmol) and PdCl2(dppf) (0.014 g, 0.019 mmol) in dioxane (8 mL) and aqueous saturated NaHCO3 (2 mL). The resulting light brown suspension was heated at 140° C. for 45 minutes in a microwave reactor. The reaction mixture was subsequently concentrated and the crude residue was purified by preparative HPLC, eluting with a gradient of 35-40% ACN (containing 0.035% TFA) in H2O (containing 0.05% TFA) over a period of 8 minutes. The volatiles were removed in vacuo to give a TFA salt of the title compound as white solid (0.043 g, 39%). 1H NMR (400 MHz, DMSO-d6) δ ppm 4.03 (s, 3H), 7.60 (d, J=1.01 Hz, 1H), 8.00 (s, 1H), 8.34-8.52 (m, 1H), 9.06 (s, 2H); ESI-MS m/z [M+1-1]′ calc'd for C13H9F3N4O, 295.1. found 295.15.

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-29f70cdbeb674b7c88130f81f9b812c6
出典メモuspto-grants-2016_09