化工社化工社 化学情報印刷レポート · 研究参考用
HRID 962516作成日:2026年10月25日
Methanimidamide, hydrochloride (1:1) → 6,7-Dihydro-7-(4-nitrobenzoyl)-5H-pyrimido[5,4-d][1]benzazepine
https://huagongshe.com/reaction/962516
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 Methoxide | HCID 10942334 | — |
| 反応物 | 4-[(dimethylamino)methylene]-1,2,3,4-tetrahydro-1-(4-nitrobenzoyl)-5H-1-benzazepin-5-one | HCID 53653564 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 6,7-Dihydro-7-(4-nitrobenzoyl)-5H-pyrimido[5,4-d][1]benzazepine | HCID 54528139 | 107.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US05760031 |
|---|
| 出典データセット | uspto-grants-1998_06 |
|---|
| ORD ID | ord-ff591c69c9474e40b2e342c9580c182b |
|---|
| 出典メモ | uspto-grants-1998_06 |
|---|