Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 355855생성일: 2026년 10월 25일
Methanimidamide, hydrochloride (1:1) → 6,7-Dihydro-7-(4-nitrobenzoyl)-5H-pyrimido[5,4-d][1]benzazepine
https://huagongshe.com/reaction/355855
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methanimidamide, hydrochloride (1:1) | HCID 10313058 | — |
| 반응물 | Sodium Methoxide | HCID 10942334 | — |
| 반응물 | 4-[(dimethylamino)methylene]-1,2,3,4-tetrahydro-1-(4-nitrobenzoyl)-5H-1-benzazepin-5-one | HCID 53653564 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | 6,7-Dihydro-7-(4-nitrobenzoyl)-5H-pyrimido[5,4-d][1]benzazepine | HCID 54528139 | 107.7% |
반응 단계
To a solution of 0.152 g (1.89 mmol) of formamidine hydrochloride in 10 ml of methanol under argon is added 0.102 g (1.89 mmol) of sodium methoxide. After stirring 5 min., a solution of 0.46 g (1.26 mmol) of 4-[(dimethylamino)methylene]-1,2,3,4-tetrahydro-1-(4-nitrobenzoyl)-5H-1-benzazepine-5-one in 5 ml of methanol is added and the mixture stirred 18 hours. The solvent is removed, dichloromethane added, and the mixture filtered. The solid is washed with dichloromethane. The combined filtrate is concentrated to dryness to give 0.47 g of tan foam. The preceding solid is purified by chromatography on silica gel. The compound is dissolved in ethyl acetate-dichloromethane and applied to the column. The column is then eluted with ethyl acetate to give 0.25 g of product as pale yellow crystals.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05834461 |
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| 출처 데이터셋 | uspto-grants-1998_11 |
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| ORD ID | ord-d5d7883725784826a03e5dfff1f4d9f6 |
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| 출처 메모 | uspto-grants-1998_11 |
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