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HRID 2306297作成日:2026年10月26日

Triethylamine → 3-cyclopentyl-2-(3,4-dichloro-phenyl)-N-quinolin-2-yl-propionamide

https://huagongshe.com/reaction/2306297

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物2-AminoquinolineHCID 11379—
反応物Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
反応物3-cyclopentyl-2-(3,4-dichlorophenyl)propanoic AcidHCID 2762725—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物3-cyclopentyl-2-(3,4-dichloro-phenyl)-N-quinolin-2-yl-propionamideHCID 1022345550%

反応手順

A solution of 3-cyclopentyl-2-(3,4-dichlorophenyl)-propionic acid (prepared as in Example 1, 100 mg, 0.34 mmol), benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate (166 mg, 0.38 mmol), triethylamine (0.096 mL, 0.68 mmol), and 2-aminoquinoline (75 mg, 0.52 mmol) in dry N,N-dimethylformamide (2 mL) was stirred at 25° C. for 14 h. The reaction mixture was then diluted with water and ethyl acetate, and the layers were separated. The organic layer was sequentially washed with a saturated aqueous sodium bicarbonate solution, water, and a saturated aqueous sodium chloride solution. The organic layer was dried over magnesium sulfate, filtered, and concentrated in vacuo. Flash chromatography (Merck Silica gel 60, 230-400 mesh, 4/1 hexanes/ethyl acetate) afforded 3-cyclopentyl-2-(3,4-dichloro-phenyl)-N-quinolin-2-yl-propionamide (70 mg, 50%) as a white foam: mp 172-173° C.; EI-HRMS m/e calcd for C23H22Cl2N2O (M+) 412.1109, found 412.1108.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06441184B1
出典データセットuspto-grants-2002_08
ORD IDord-ee542903819c4c5a80764b2e43421ea2
出典メモuspto-grants-2002_08