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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

反応式

関与物質

役割名称HCID仕込み量
反応物N-MethylethylenediamineHCID 8014—
反応物Diethyl [2-(2-Fluorophenyl)-2-oxoethyl]phosphonateHCID 86585808—
溶媒PyridineHCID 1049—
生成物(1-Methyl-1,2,3,4-tetrahydrobenzo[e][1,4]diazepin-5-ylidenemethyl)phosphonic acid diethyl esterHCID 7295724326.6%

反応条件

温度95 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US06703387B2
出典データセットuspto-grants-2004_03
ORD IDord-deca01e94d734623854fc9a21f58b731
出典メモuspto-grants-2004_03