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HRID 48321作成日:2026年10月24日
N-Methylethylenediamine → (1-Methyl-1,2,3,4-tetrahydrobenzo[e][1,4]diazepin-5-ylidenemethyl)phosphonic acid diethyl ester
https://huagongshe.com/ja/reaction/48321
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | N-Methylethylenediamine | HCID 8014 | — |
| 反応物 | Diethyl [2-(2-Fluorophenyl)-2-oxoethyl]phosphonate | HCID 86585808 | — |
| 溶媒 | Pyridine | HCID 1049 | — |
| 生成物 | (1-Methyl-1,2,3,4-tetrahydrobenzo[e][1,4]diazepin-5-ylidenemethyl)phosphonic acid diethyl ester | HCID 72957243 | 26.6% |
反応手順
A mixture of 10.45 g (38.1 mmol) of [2-(2-fluorophenyl)-2-oxoethyl]phosphonic acid diethyl ester and 14.1 g (190 mmol) N-methylethylenediamine in 100 ml of pyridine was heated at 95° C. for 18 hours. The solvent was evaporated and the residue was partitioned between 200 ml of water and 2×100 ml of dichloromethane. The combined organic portions were dried (magnesium sulphate), filtered and evaporated. The residue was purified by column chromatography eluting with 5% methanol/dichloromethane to give 3.14 g (26%) of (1-methyl-1,2,3,4-tetrahydrobenzo[e][1,4]diazepin-5-ylidenemethyl)phosphonic acid diethyl ester as a light brown oil; MS: m/e 311.0 [M+H]+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06703387B2 |
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| 出典データセット | uspto-grants-2004_03 |
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| ORD ID | ord-deca01e94d734623854fc9a21f58b731 |
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| 出典メモ | uspto-grants-2004_03 |
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