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HRID 330623作成日:2026年10月26日

Triethylamine → N-[1(R)-ethoxycarbonyl-8-phthalimidooctyl]-L-alanyl-L-proline tertiary butylester

https://huagongshe.com/reaction/330623

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物tert-Butyl L-alanyl-L-prolinateHCID 12939800—
反応物Ethyl 2-bromo-9-phthalimidononanoateHCID 13622534—
溶媒AcetonitrileHCID 6342—
生成物N-[1(R)-ethoxycarbonyl-8-phthalimidooctyl]-L-alanyl-L-proline tertiary butylesterHCID 1592768813.1%

反応手順

A solution of ethyl 2-bromo-9-phthalimidononanoate [prepared according to Chem. Pharm. Bull. 34, 2078 (1986)] (3 g), L-alanyl-L-proline tertiary butylester (1 g) and triethylamine (0.8 ml) in acetonitrile (200 ml) is subjected to 60 hours' reflux. Acetonitrile is distilled off under reduced pressure, and the residue is dissolved in ethyl acetate. The solution is dehydrated with anhydrous sodium sulfate, and thereafter is concentrated to obtain an oily residue. When this substance is applied to a silica gel chromatography (ethyl acetate:n-hexane=3:1) for separative purification, 310 mg of N-[1(R)-ethoxycarbonyl-8-phthalimidooctyl]-L-alanyl-L-proline tertiary butylester is obtained as a colorless oil from the first effluence.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04897483
出典データセットuspto-grants-1990_01
ORD IDord-634fc89166d84c45b81d6c9f9789ba58
出典メモuspto-grants-1990_01