戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 355855作成日:2026年10月26日

Methanimidamide, hydrochloride (1:1) → 6,7-Dihydro-7-(4-nitrobenzoyl)-5H-pyrimido[5,4-d][1]benzazepine

https://huagongshe.com/reaction/355855

反応式

関与物質

役割名称HCID仕込み量
反応物Methanimidamide, hydrochloride (1:1)HCID 10313058—
反応物Sodium MethoxideHCID 10942334—
反応物4-[(dimethylamino)methylene]-1,2,3,4-tetrahydro-1-(4-nitrobenzoyl)-5H-1-benzazepin-5-oneHCID 53653564—
溶媒MethanolHCID 887—
生成物6,7-Dihydro-7-(4-nitrobenzoyl)-5H-pyrimido[5,4-d][1]benzazepineHCID 54528139107.7%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05834461
出典データセットuspto-grants-1998_11
ORD IDord-d5d7883725784826a03e5dfff1f4d9f6
出典メモuspto-grants-1998_11