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HRID 398473作成日:2026年10月25日

2-Aminopyridine → 3-cyclopentyl-2-(3,4-dichlorophenyl)-N-pyridin-2-ylpropanamide

https://huagongshe.com/reaction/398473

反応式

関与物質

役割名称HCID仕込み量
反応物2-AminopyridineHCID 10439—
反応物Oxalyl chlorideHCID 65578—
反応物DiisopropylethylamineHCID 81531—
反応物3-cyclopentyl-2-(3,4-dichlorophenyl)propanoic AcidHCID 2762725—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
溶媒TetrahydrofuranHCID 8028—
生成物3-cyclopentyl-2-(3,4-dichlorophenyl)-N-pyridin-2-ylpropanamideHCID 276272650%

反応条件

温度0 °C

反応手順

A solution of 3-cyclopentyl-2-(3,4-dichlorophenyl)-propionic acid (114 mg, 0.39 mmol) in methylene chloride (10 mL) was treated with I drop of N,N-dimethylformamide and then cooled to 0° C. The reaction mixture was then treated with a 2.0M solution of oxalyl chloride in methylene chloride (0.22 mL, 0.44 mmol). The reaction mixture was stirred at 0° C. for 30 min and then treated with a solution of 2-aminopyridine (78 mg, 0.83 mmol) and N,N-diisopropylethylamine (0.16 mL, 0.95 mmol) in tetrahydrofuran (2 mL). The resulting reaction mixture was stirred at 25° C. for 14 h. The reaction mixture was then diluted with water (10 mL) and extracted with methylene chloride (2×15 mL). The combined organic layers were dried over sodium sulfate, filtered, and concentrated in vacuo. Flash chromatography (Merck Silica gel 60, 230-400 mesh, hexanes then 19/1 to 4/1 hexanes/ethyl acetate) afforded 3-cyclopentyl-2-(3,4-dichloro-phenyl)-N-pyridin-2-yl-propionamide (58 mg, 50%) as a white foam: EI-HRMS m/e calcd for C19H20Cl2N2O (M+) 362.0953, found 362.0955.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06610846B1
出典データセットuspto-grants-2003_08
ORD IDord-300a0ea941e04a768cedb19bb2bd8386
出典メモuspto-grants-2003_08