戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 643812作成日:2026年10月27日

1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride → tert-butyl L-prolinate

https://huagongshe.com/reaction/643812

反応式

関与物質

役割名称HCID仕込み量
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
反応物5-[(4-Phenylphenoxy)methyl]furan-2-carboxylic acidHCID 4683153—
反応物tert-butyl (2R)-pyrrolidine-2-carboxylate hydrochlorideHCID 44629909—
溶媒TetrahydrofuranHCID 8028—
生成物tert-butyl L-prolinateHCID 10288461.1%

反応手順

A solution of 5-(biphenyl-4-yloxymethyl)-furan-2-carboxylic acid (of Intermediate 8; 0.134 g, 0.46 mmol), D-proline tert-butyl ester hydrochloride (Bachem; 0.22 g, 1.1 mmol), 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide hydrochloride (Avocado; 0.18 g, 0.95 mmol), and N,N-dimethylaminopyridine (0.166 g, 1.36 mmol) in tetrahydrofuran (10 mL) was stirred at room temperature for 16 h. The solvents were evaporated under reduced pressure, and water and ethyl acetate were added. The aqueous phase was extracted three times with ethyl acetate, and the combined organic layers were dried (sodium sulfate), filtered, evaporated, and purified using a Biotage Flash 40 purification system, eluting with methylene chloride/acetone 9:1, to give 5-(biphenyl-4-yloxymethyl)-furan-2-carbonyl]-D-pyrrolidine-2-carboxylic acid tert-butyl ester as a white solid (0.115 g, 56%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07700632B2
出典データセットuspto-grants-2010_04
ORD IDord-4b55ed77f1a04cefaed8fcc07fbb4178
出典メモuspto-grants-2010_04