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HRID 649516作成日:2026年10月26日

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

https://huagongshe.com/reaction/649516

反応式

関与物質

役割名称HCID仕込み量
反応物MorpholineHCID 8083—
反応物Ethyl AcetateHCID 8857—
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TolueneHCID 1140—
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) in 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US04740508
出典データセットuspto-grants-1988_04
ORD IDord-4648a55d15244d76ace79333858c27d1
出典メモuspto-grants-1988_04