戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 26035作成日:2026年10月26日

Triethylamine → 5-Amino-2,10-dimethyl-4,8-dioxo-5-vinyl-3,9-diazaundecanedioic acid

https://huagongshe.com/reaction/26035

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Ethyl chloroformateHCID 10928—
反応物L-Alanine methyl esterHCID 82335—
反応物2-(Benzyloxycarbonyl)amino-2-vinylglutaric acidHCID 21326441—
溶媒DichloromethaneHCID 6344—
生成物5-Amino-2,10-dimethyl-4,8-dioxo-5-vinyl-3,9-diazaundecanedioic acidHCID 21326422—

反応条件

温度25 °C

反応手順

To 2-(benzyloxycarbonyl)amino-2-vinylglutaric acid (305 mg, 1 mM) in methylene chloride (15 ml) is added triethylamine (205 mg, 2 mM) followed by ethyl chloroformate (218 mg, 2 mM). The solution is stirred for one hour at 25° C., then alanine methyl ester (206 mg, 2 mM) in methylene chloride (5 ml) is added. This solution is kept overnight at 25° C., washed with water, dried and evaporated to dryness. The residue is treated with 5 ml of a 40% (w/w) solution of hydrogen bromide in dioxane at 25° C. for 30 minutes. Ether (50 ml) is then added and the precipitate collected. This is then treated with 20 ml of a 1 N sodium hydroxide solution overnight at 25° C., the pH adjusted to 6.5, and applied to an Amberlite 120 H+ resin. Elution with 2 N ammonium hydroxide afforded 5-amino-2,10-dimethyl-4,8-dioxo-5-vinyl-3,9-diazaundecanedioic acid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04147873
出典データセットuspto-grants-1979_04
ORD IDord-dbca350db4ff403ca0a0c18ad91427fb
出典メモuspto-grants-1979_04