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HRID 12883作成日:2026年10月24日

2-Propenoic acid, 2-cyano-3-ethoxy-, ethyl ester → ethyl 5-amino-1-(oxan-4-yl)-1H-pyrazole-4-carboxylate

https://huagongshe.com/ja/reaction/12883

反応式

関与物質

役割名称HCID仕込み量
反応物2-Propenoic acid, 2-cyano-3-ethoxy-, ethyl esterHCID 78943—
反応物Sodium AcetateHCID 517045—
反応物(Oxan-4-yl)hydrazine hydrochlorideHCID 17773358—
溶媒EthanolHCID 702—
生成物ethyl 5-amino-1-(oxan-4-yl)-1H-pyrazole-4-carboxylateHCID 6702077492.3%

反応条件

温度82.5 °C

反応手順

(Tetrahydro-pyran-4-yl)-hydrazine hydrochloride (1.975 g, 12.94 mmol), ethyl (ethoxymethylene)-cyanoacetate (1.958 g, 11.57 mmol) and sodium acetate (1.370 g; 16.70 mmol) were combined in ethanol (16 mL). The mixture was heated at 80-85° C. for 17 hours. After cooling to room temperature, the reaction was concentrated and the residue was partitioned between methylene chloride and water. The organic phase was separated and washed with water and then brine. Each aqueous phase was back extracted with methylene chloride. The two organic phases were combined, dried over sodium sulfate and concentrated in vacuo. The crude material was purified by flash chromatography eluting with 60-100% ethyl acetate/hexanes to give 5-amino-1-(tetrahydro-pyran-4-yl)-1H-pyrazole-4-carboxylic acid ethyl ester (2.554 g, 92%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07728029B2
出典データセットuspto-grants-2010_06
ORD IDord-6f68aa42048a4899b155725c5423f581
出典メモuspto-grants-2010_06