戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 332837作成日:2026年10月26日

Sulfuric Acid → 5-(((1R,2S)-2-aminocyclohexyl)amino)-3-((5-fluoropyridin-3-yl)amino)pyrazine-2-carboxamide

https://huagongshe.com/reaction/332837

反応式

関与物質

役割名称HCID仕込み量
反応物Sulfuric AcidHCID 1118—
反応物Cesium carbonateHCID 10796—
反応物5-Fluoro-3-pyridinamineHCID 574450—
反応物Binap, (A+-)-HCID 634876—
反応物HCID 86685625HCID 86685625—
触媒palladium(II) acetateHCID 167845—
溶媒WaterHCID 962—
溶媒Trifluoroacetic acidHCID 6422—
溶媒1,4-DioxaneHCID 31275—
生成物5-(((1R,2S)-2-aminocyclohexyl)amino)-3-((5-fluoropyridin-3-yl)amino)pyrazine-2-carboxamideHCID 8668562885.8%

反応条件

温度110 °C

反応手順

The mixture of tert-tutyl ((1S,2R)-2-((6-chloro-5-cyanopyrazin-2-yl)amino)cyclohexyl)carbamate (100 mg, 0.28 mmol), 3-fluoro-5-aminopyridine (60 mg, 0.56 mmol), powder cesium carbonate (360 mg, 1.12 mmol), BINAP (37 mg, 0.06 mmol), Pd(OAc)2 (14 mg, 0.06 mmol) in 20 mL dioxane was degassed with argon stream. It was stirred in argon atmosphere at 110° C. for 2 h. The mixture was cooled, diluted with 100 mL EtOAc, vigorously stirred, and filtered through celite. The filtrate was concentrated and subjected to silica flash column with 0-60% EtOAc in hexane to isolate the coupling product. It was then stirred in 6 mL TFA and 1 mL conc. H2SO4 at 80° C. for 30 m. It was cooled in ice bath, diluted with water, filtered, and subjected to reverse phase preparative HPLC to isolate the title compound (83 mg). MS found for C16H20FN7O as (M+H)+ 346.5. UV: λ=259, 301 nm. 1H NMR: (CD3OD) δ 9.04 (1H, m), 8.57 (1H, m), 8.40 (1H, m), 7.73 (1H, s), 4.49 (1H, m), 3.74 (1H, m), 1.96-1.60 (8H, m) ppm.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08877760B2
出典データセットuspto-grants-2014_11
ORD IDord-29df8ee851fc429f83591399850729bf
出典メモuspto-grants-2014_11