戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 519621作成日:2026年10月25日

3-Ethoxy-2-methyl-3-oxopropane-1-diazonium → HCID 178438641、化合物

https://huagongshe.com/reaction/519621

反応式

関与物質

役割名称HCID仕込み量
反応物3-Ethoxy-2-methyl-3-oxopropane-1-diazoniumHCID 86644035—
反応物HCID 178438592HCID 178438592—
触媒HCID 178476747HCID 178476747—
溶媒TolueneHCID 1140—
生成物HCID 178438641HCID 17843864189%

反応手順

To a mixture of 4′-{[4-(trans-4-hydroxycyclohexyl)-5-oxo-7-propyl-4,5-dihydro[1,2,4]triazolo[1,5-a]pyrimidin-6-yl]methyl}biphenyl-2-carbonitrile (4 g), rhodium(I) acetate (0.028 g) and toluene (70 mL) was added dropwise a solution (10 mL) of 3-ethoxy-2-methyl-3-oxopropane-1-diazonium (5.5 mL) in toluene at 80° C., and the mixture was stirred at the same temperature for 1 hr. The reaction mixture was concentrated, and the obtained residue was purified by silica gel column chromatography. The obtained residue was dissolved in tetrahydrofuran (20 mL) and methanol (20 mL), and 1N aqueous sodium hydroxide solution (20 mL) was added. The reaction mixture was stirred for 1 hr, 1N aqueous hydrochloric acid solution was added, and the mixture was extracted with ethyl acetate. The obtained ethyl acetate layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography to give the title compound as a colorless solid (4.1 g, 89%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09115136B2
出典データセットuspto-grants-2015_08
ORD IDord-1a9e26cb03544b168892c6f25fdac07f
出典メモuspto-grants-2015_08