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HRID 1688430作成日:2026年10月25日

Pyridine → 3'-Fluoro-4'-[(5-oxo-4-phenyl-7-propyl-4,5-dihydro[1,2,4]triazolo[1,5-a]pyrimidin-6-yl)methyl]biphenyl-2-carbonitrile

https://huagongshe.com/reaction/1688430

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物TriethylamineHCID 8471—
反応物Phenylboronic AcidHCID 66827—
反応物3'-Fluoro-4'-[(5-oxo-7-propyl-4,5-dihydro[1,2,4]triazolo[1,5-a]pyrimidin-6-yl)methyl]biphenyl-2-carbonitrileHCID 136337139—
触媒Cupric acetateHCID 8895—
溶媒DichloromethaneHCID 6344—
溶媒Ethyl AcetateHCID 8857—
生成物3'-Fluoro-4'-[(5-oxo-4-phenyl-7-propyl-4,5-dihydro[1,2,4]triazolo[1,5-a]pyrimidin-6-yl)methyl]biphenyl-2-carbonitrileHCID 67010029102%

反応手順

To a suspension (20 mL) of 3′-fluoro-4′-[(5-oxo-7-propyl-4,5-dihydro[1,2,4]triazolo[1,5-a]pyrimidin-6-yl)methyl]biphenyl-2-carbonitrile (0.5 g), phenylboronic acid (0.31 g), triethylamine (0.5 mL), pyridine (1 mL) and molecular sieves 4A (1 g) in dichloromethane was added copper(II) acetate (0.47 g), and the mixture was stirred for 16 hr. The reaction mixture was diluted with ethyl acetate, insoluble material was filtered off through celite, and the filtrate was concentrated. The residue was purified by silica gel column chromatography to give the title compound as a colorless solid (0.61 g, 100%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08148383B2
出典データセットuspto-grants-2012_04
ORD IDord-c40a57e412004fd7add46fc202723e85
出典メモuspto-grants-2012_04