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HRID 217772作成日:2026年10月25日

Sodium Carbonate → 3-Amino-6-(4-(3-(tert-butyldimethylsilyloxy)propyl)phenyl)-N-(pyridin-3-yl)-pyrazine-2-carboxamide

https://huagongshe.com/reaction/217772

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Potassium AcetateHCID 517044—
反応物Bis(pinacolato)diboraneHCID 2733548—
反応物3-Amino-6-bromo-N-pyridin-3-ylpyrazine-2-carboxamideHCID 10402162—
反応物HCID 15342962HCID 15342962—
触媒Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
溶媒WaterHCID 962—
溶媒1,4-DioxaneHCID 31275—
生成物3-Amino-6-(4-(3-(tert-butyldimethylsilyloxy)propyl)phenyl)-N-(pyridin-3-yl)-pyrazine-2-carboxamideHCID 6667865062.3%

反応手順

A mixture of the product of step (ii) (9.84 g, 30 mmol), bis(pinacolato)diboron (11.4 g, 45 mmol), KOAc (9 g, 90 mmol) and Pd(dppf)Cl2 (1 g, 1.5 mmol) in dioxane (200 mL) was stirred and degassed with N2 (×3). The mixture was stirred at 80° C. under a N2 atmosphere for 3 hours. The reaction mixture was cooled to room temperature. Water (25 mL) and Na2CO3 (10 g, 90 mmol) were added to the mixture. The mixture was stirred for 10 minutes before the product of step (v) (7.9 g, 27 mmol) and Pd(dppf)Cl2 (0.5 g, 0.7 mmol) were added. The resulting solution was degassed again with N2 (×3). The reaction mixture was stirred at 90° C. under a N2 atmosphere for additional 10 hours. Na2SO4 was added, filtered and the filtrate concentrated in vacuo. The crude product was purified by column chromatography with PE:EtOAc=5:1 to 3:1 as eluent to afford the subtitle compound (vi) as a yellow solid (7.8 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08198285B2
出典データセットuspto-grants-2012_06
ORD IDord-8f06ac597e2842a492e02395d14ac654
出典メモuspto-grants-2012_06