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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1794387생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1794387

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl p-aminobenzylphosphonateHCID 88358—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물1-Hydroxybenzotriazole hydrateHCID 2796029—
반응물4-(5-Phenyl-4-isoxazolyl)butanoic acidHCID 22221097—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물N-(4-diethylphosphonomethylphenyl)-4-(5-phenyl-4-isoxazolyl)butaneamideHCID 2222101094%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07022725B2
출처 데이터셋uspto-grants-2006_04
ORD IDord-dd92d1ef88424fa58437d06829105446
출처 메모uspto-grants-2006_04