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HRID 2253394作成日:2026年10月27日

1,2-Diaminocyclohexane → N4-(2-Ethylpyrazolo[1,5-a]pyridin-3-yl)tetrahydro-2H-4-pyrancarboxamide

https://huagongshe.com/reaction/2253394

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-DiaminocyclohexaneHCID 4610—
反応物Potassium Phosphate, TribasicHCID 62657—
反応物Oxane-4-carboxamideHCID 13197203—
反応物2-Ethyl-3-iodopyrazolo[1,5-a]pyridineHCID 16114933—
触媒Copper iodideHCID 83717—
溶媒O-XyleneHCID 7237—
生成物N4-(2-Ethylpyrazolo[1,5-a]pyridin-3-yl)tetrahydro-2H-4-pyrancarboxamideHCID 2108412179.6%

反応条件

温度120 °C

反応手順

A mixture of 2-ethyl-3-iodopyrazolo[1,5-a]pyridine (350 g, 1.29 mol), tetrahydro-2H-4-pyrancarboxamide (249 g, 1.93 mol), copper iodide (49.0 g, 258 mmol), tripotassium phosphate (hydrate) (546 g, 2.57 mol), 1,2-cyclohexanediamine (mixture of cis and trans) (58.7 g, 514 mmol) and xylene (3500 mL) was stirred while heating at an external temperature of 120° C. (oil bath). The reaction mixture was heated and stirred for 6 hours, and then heating was terminated and upon reaching an internal temperature of 61.5° C., hot water (58° C., 3500 mL) was added to the reaction mixture and stirring was continued overnight. After adding 28% aqueous ammonia (1050 mL) to the reaction mixture and stirring for 1 hour, the precipitate was filtered out and washed with water (1750 mL) and ethyl acetate (1050 mL) and then dried under aeration at 60° C. overnight to afford 280 g of the title compound (major conformer:minor conformer=6:1) (79.6% yield)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07323569B2
出典データセットuspto-grants-2008_01
ORD IDord-1194045c4b864185a2bd2356a0a32c28
出典メモuspto-grants-2008_01