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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5583생성일: 2026년 10월 23일

Triethyl phosphonoacetate → 5-ethoxycarbonylmethylidene-7-chloro-1-[2-methyl-4-(2-methylbenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzazepine

https://huagongshe.com/ko/reaction/5583

반응식

참여 물질

역할이름HCID투입량
반응물Triethyl phosphonoacetateHCID 13345—
반응물Sodium hydrideHCID 24758—
반응물5-Dehydro TolvaptanHCID 11362843—
용매TetrahydrofuranHCID 8028—
생성물5-ethoxycarbonylmethylidene-7-chloro-1-[2-methyl-4-(2-methylbenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzazepineHCID 54237705—

반응 단계

To tetrahydrofuran (200 ml) is added sodium hydride (60%, 0.85 g), and thereto is added dropwise ethyl diethylphosphonoacetate (4.68 ml) with stirring under ice-cooling, and the mixture is further stirred under ice-cooling for 10 minutes. To the reaction mixture is added 5-oxo-7-chloro-1-[2-methyl-4-(2-methylbenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzazepine (2.10 g), and the mixture is stirred at room temperature for 6 hours. The reaction solution is poured into ice-water (200 ml), and extracted with ethyl acetate (300 ml). The extract is washed with brine (300 ml), dried over magnesium sulfate, and the solvent is distilled off. The resulting residue is purified by silica gel column chromatography (eluent; ethyl acetate: n-hexane=1:2) to give 5-ethoxycarbonylmethylidene-7-chloro-1-[2-methyl-4-(2-methylbenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzazepine (2.22 g) in the form of a mixture of the E-type compound and the Z-type compound thereof, as colorless amorphous.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05244898
출처 데이터셋uspto-grants-1993_09
ORD IDord-2aaa607f367b4114b06385b6e442d470
출처 메모uspto-grants-1993_09