戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 23215作成日:2026年10月26日

3-Methoxybenzylamine → tert-Butyl (1S,2R)-1-(3,5-difluorobenzyl)-2-hydroxy-3-[(3-methoxybenzyl)amino]propylcarbamate

https://huagongshe.com/reaction/23215

反応式

関与物質

役割名称HCID仕込み量
反応物3-MethoxybenzylamineHCID 21156—
反応物tert-Butyl ((S)-2-(3,5-difluorophenyl)-1-((S)-oxiran-2-yl)ethyl)carbamateHCID 9922319—
溶媒IsopropanolHCID 3776—
生成物tert-Butyl (1S,2R)-1-(3,5-difluorobenzyl)-2-hydroxy-3-[(3-methoxybenzyl)amino]propylcarbamateHCID 11441951—

反応手順

tert-Butyl (1S)-2-(3,5-difluorophenyl)-1-[(2S)-oxiranyl]ethylcarbamate (V, EXAMPLE 4, 245 mg, 0.82 mmol) is suspended in isopropyl alcohol (6 mL) and 3-methoxybenzylamine (160 μL, 1.22 mmol) is added with stirring at 20-25°. This mixture is heated to gentle reflux (bath temp 85°) under nitrogen for 2 hr, whereupon the resulting mixture is concentrated under reduced pressure to give the title compound. The title compound is purified by flash chromatography (2-5% methanol/methylene chloride; gradient elution) to give purified title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06849750B2
出典データセットuspto-grants-2005_02
ORD IDord-ff0030a04151401aa4814d61e81628e9
出典メモuspto-grants-2005_02