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HRID 1351420作成日:2026年10月25日

Sulfuric acid magnesium salt (1:1) → 3-nitrooxypropyl (2S)-1-[(2S)-2-[[(2S)-1-ethoxy-1-oxo-4-phenylbutan-2-yl]amino]propanoyl]pyrrolidine-2-carboxylate

https://huagongshe.com/reaction/1351420

反応式

関与物質

役割名称HCID仕込み量
反応物Sulfuric acid magnesium salt (1:1)HCID 24083—
反応物Sodium BicarbonateHCID 516892—
反応物N-[1(S)-Ethoxycarbonyl-3-phenylpropyl]-L-alanineHCID 5702571—
反応物L-proline 3-nitrooxypropyl esterHCID 11672975—
溶媒Ethyl AcetateHCID 8857—
溶媒Sodium chloride; waterHCID 57417360—
生成物3-nitrooxypropyl (2S)-1-[(2S)-2-[[(2S)-1-ethoxy-1-oxo-4-phenylbutan-2-yl]amino]propanoyl]pyrrolidine-2-carboxylateHCID 1167734340.9%

反応手順

To a suspension of 1,1-carbonylimidazole (22 g, 136 mmol) in EtOAc (150 mL) a solution of commercial N-[(1S)-1-(ethoxycarbonyl)-3-phenylpropyl]-L-alanine (20.2 g, 72.32 mmol) in EtOAc (100 mL) was added dropwise in 10 minutes. The resulting solution was stirred at room temperature for 1 hour then L-proline 3-nitrooxypropyl ester (28.8 g, 113 mmol) was added and the mixture was stirred for 16 hours. Then was treated with saturated NaHCO3 and brine. The organic layer was anhydrified with magnesium sulphate and concentrated. The residue was purified by flash chromatography (nHexane/EtOAc 4:6) affording N-[(1S)-1-(ethoxycarbonyl)-3-phenylpropyl]-L-alanyl-L-proline 3-nitrooxypropyl ester (14.2 g, 26%) as a pale yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07217733B2
出典データセットuspto-grants-2007_05
ORD IDord-abecd63970f94866a4fdd07e72aa2ee9
出典メモuspto-grants-2007_05