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HRID 520678作成日:2026年10月24日

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → 4-((6-(1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxamido)pyridin-3-yl)oxy)picolinamide

https://huagongshe.com/ja/reaction/520678

反応式

関与物質

役割名称HCID仕込み量
反応物1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
反応物HOAtHCID 181649—
反応物Antipyric acidHCID 246564—
反応物HCID 90031028HCID 90031028—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物4-((6-(1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxamido)pyridin-3-yl)oxy)picolinamideHCID 7305326625%

反応条件

温度45 °C

反応手順

To a suspension of 4-((6-aminopyridin-3-yl)oxy)picolinamide (230 mg, 1 mmol) and 1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxylic acid (237 mg, 1.02 mmol) in DCM (5 mL) was added EDCI (230 mg, 1.2 mmol) and HOAT (27 mg, 0.2 mmol). The reaction was stirred at 45° C. for 28 hours, then cooled to rt and diluted with water (10 mL) and DCM (20 mL). The organic phase was concentrated in vacuo and the residue was purified by a silica gel column chromatography (DCM/CH3OH (v/v)=40/1) to give the title compound as a light grey solid (111 mg, 25%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09326975B2
出典データセットuspto-grants-2016_05
ORD IDord-1619e4cb056440a19f65efca89f1c326
出典メモuspto-grants-2016_05