戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 620039作成日:2026年10月24日

Toluene → 1-[[Methyl[(S)-3-[(4-morpholinylcarbonyl)amino]-2-oxo-4-phenylbutyl]amino]carbonyl]-L-proline, phenylmethyl ester

https://huagongshe.com/ja/reaction/620039

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物MorpholineHCID 8083—
反応物Benzyl L-prolinateHCID 736155—
反応物1-[[[(S)-3-[[(4-nitrophenoxy)carbonyl]amino]-2-oxo-4-phenylbutyl]methylamino]carbonyl]-L-proline, phenylmethyl esterHCID 14127226—
溶媒Ethyl AcetateHCID 8857—
生成物1-[[Methyl[(S)-3-[(4-morpholinylcarbonyl)amino]-2-oxo-4-phenylbutyl]amino]carbonyl]-L-proline, phenylmethyl esterHCID 14499496—

反応手順

Morpholine (1 ml., 11.4 mmole) is added to a stirring solution of 1-[[[(S)-3-[[(4-nitrophenoxy)carbonyl]amino]-2-oxo-4-phenylbutyl]methylamino]carbonyl]-L-proline, phenylmethyl ester (0.9 g., 1.58 mmole) ih toluene at 0° in one portion. The reaction mixture turns yellow in 15 minutes and TLC indicates complete loss of starting material after 30 minutes. The resulting solution is washed sequentially with water, 1N hydrochloric acid, and 10% sodium bicarbonate. The organic layer is dried (MgSO4) and concentrated. The crude product is purified by preparative layer chromatography to give 0.26 g. of 1-[[methyl[(S)-3-[(4-morpholinylcarbonyl)amino]carbonyl]-2-oxo-4-phenylbutyl]amino]carbonyl]L-proline, phenylmethyl ester as a yellow oil. TLC (ethyl acetate) Rf =0.18.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04818757
出典データセットuspto-grants-1989_04
ORD IDord-e48ef4dda9a74b3489f5acecf41d1a4b
出典メモuspto-grants-1989_04