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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Triethyl phosphonoacetate | HCID 13345 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 5-Dehydro Tolvaptan | HCID 11362843 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 5-ethoxycarbonylmethylidene-7-chloro-1-[2-methyl-4-(2-methylbenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzazepine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05244898 |
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| 출처 데이터셋 | uspto-grants-1993_09 |
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| ORD ID | ord-2aaa607f367b4114b06385b6e442d470 |
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| 출처 메모 | uspto-grants-1993_09 |
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