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HRID 1844452作成日:2026年10月27日

Ethyl Acetate → 1-methyl-5-(2-morpholin-4-yl-[1,2,4]triazolo[1,5-a]pyridin-6-ylcarbamoyl)-1H-pyrazole-4-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1844452

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物DiisopropylethylamineHCID 81531—
反応物Propylphosphoric anhydrideHCID 16167369—
反応物4-(Ethoxycarbonyl)-1-methyl-1H-pyrazole-5-carboxylic acidHCID 25247567—
反応物2-Morpholin-4-yl-[1,2,4]triazolo[1,5-a]pyridin-6-amineHCID 89464404—
溶媒TetrahydrofuranHCID 8028—
生成物1-methyl-5-(2-morpholin-4-yl-[1,2,4]triazolo[1,5-a]pyridin-6-ylcarbamoyl)-1H-pyrazole-4-carboxylic acid ethyl esterHCID 8946472171%

反応手順

A mixture of 2-morpholin-4-yl-[1,2,4]triazolo[1,5-a]pyridin-6-amine (225 mg, 1.03 mmol), 4-(ethoxycarbonyl)-1-methyl-1H-pyrazole-5-carboxylic acid (224 mg, 1.13 mmol), propylphosphonic anhydride in ethyl acetate 50% (1.63 g, 1.51 ml, 2.57 mmol) and N,N-diisopropylethylamine (398 mg, 524 μl, 3.08 mmol) in tetrahydrofuran (7 ml) was refluxed for 18 hours. The solvent was evaporated, the residue was triturated with saturated aqueous sodium hydrogen carbonate. The precipitated solid was filtered off, washed with water and dried in vacuo, affording 1-methyl-5-(2-morpholin-4-yl-[1,2,4]triazolo[1,5-a]pyridin-6-ylcarbamoyl)-1H-pyrazole-4-carboxylic acid ethyl ester (292 mg, 71%) as light brown solid. Mp.: 233.5° C. MS: m/z=400.1 (M+H+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08946427B2
出典データセットuspto-grants-2015_02
ORD IDord-f61bf0aecbf54b858ce6c9cdfbeebee1
出典メモuspto-grants-2015_02