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HRID 1794387作成日:2026年10月25日

Diethyl p-aminobenzylphosphonate → N-(4-diethylphosphonomethylphenyl)-4-(5-phenyl-4-isoxazolyl)butaneamide

https://huagongshe.com/reaction/1794387

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl p-aminobenzylphosphonateHCID 88358—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
反応物1-Hydroxybenzotriazole hydrateHCID 2796029—
反応物4-(5-Phenyl-4-isoxazolyl)butanoic acidHCID 22221097—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物N-(4-diethylphosphonomethylphenyl)-4-(5-phenyl-4-isoxazolyl)butaneamideHCID 2222101094%

反応手順

A mixture of diethyl 4-aminobenzylphosphonate (1.74 g), 4-(5-phenyl-4-isoxazolyl)butanoic acid (1.38 g), 1-hydroxy-1H-1,2,3-benzotriazole hydrate (1.08 g), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (1.38 g) and N,N-dimethylformamide (20 ml) was stirred at room temperature overnight. The reaction mixture was poured into water and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with dilute hydrochloric acid, saturated aqueous sodium hydrogencarbonate and then saturated brine, dried (MgSO4) and concentrated. The residue was subjected to silica gel column chromatography, and N-(4-diethylphosphonomethylphenyl)-4-(5-phenyl-4-isoxazolyl)butaneamide (2.56 g, yield 94%) was obtained as colorless crystals from a fraction eluted with ethyl acetate-hexane (1:1, volume ratio). The crystals were recrystallized from ethyl acetate-hexane. melting point: 128–129° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07022725B2
出典データセットuspto-grants-2006_04
ORD IDord-dd92d1ef88424fa58437d06829105446
出典メモuspto-grants-2006_04