戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 519512作成日:2026年10月27日

Ethyl 2-[(2'-cyano-3-fluorobiphenyl-4-yl)methyl]-3-oxohexanoate → 3'-fluoro-4'-{[2-methyl-5-oxo-7-propyl-4-(tetrahydro-2H-thiopyran-4-yl)-4,5-dihydro[1,2,4]triazolo[1,5-a]pyrimidin-6-yl]methyl}biphenyl-2-carbonitrile

https://huagongshe.com/reaction/519512

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl 2-[(2'-cyano-3-fluorobiphenyl-4-yl)methyl]-3-oxohexanoateHCID 57460949—
反応物HCID 178434105HCID 178434105—
生成物3'-fluoro-4'-{[2-methyl-5-oxo-7-propyl-4-(tetrahydro-2H-thiopyran-4-yl)-4,5-dihydro[1,2,4]triazolo[1,5-a]pyrimidin-6-yl]methyl}biphenyl-2-carbonitrileHCID 6700842753.4%

反応条件

温度250 °C

反応手順

A mixture of ethyl 2-[(2′-cyano-3-fluorobiphenyl-4-yl)methyl]-3-oxohexanoate (1.5 g) and 5-methyl-N-(tetrahydro-2H-thiopyran-4-yl)-4H-1,2,4-triazol-3-amine (0.4 g) was stirred at 250° C. for 20 min under microwave irradiation. The obtained reaction mixture was purified by silica gel column chromatography to give the title compound as a colorless solid (0.54 g, 27%).

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-39cf7e7ec4394646911701d9e121bd2e
出典メモuspto-grants-2015_08