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HRID 1757718作成日:2026年10月23日

4-Phenylbutyric Acid → N-[2(R)-hydroxy-4-phenyl-3(S)-[[N-(4-phenylbutyryl)-L-asparaginyl]amino]butyl]-L-proline tert.butyl ester

https://huagongshe.com/ja/reaction/1757718

反応式

関与物質

役割名称HCID仕込み量
反応物4-Phenylbutyric AcidHCID 4775—
反応物EthylmorpholineHCID 7525—
反応物DicyclohexylcarbodiimideHCID 10868—
反応物N-[3(S)-[[L-asparaginyl]amino]-2(R)-hydroxy-4-phenylbutyl]-L-proline tert.butyl esterHCID 70041604—
反応物HCID 178418300HCID 178418300—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物N-[2(R)-hydroxy-4-phenyl-3(S)-[[N-(4-phenylbutyryl)-L-asparaginyl]amino]butyl]-L-proline tert.butyl esterHCID 7004365722.3%

反応手順

A solution of 270 mg of N-[3(S)-[[L-asparaginyl]amino]-2(R)-hydroxy-4-phenylbutyl]-L-proline tert.butyl ester and 98 mg of 4-phenylbutyric acid in 10 ml of dry tetrahydrofuran was cooled in an ice/salt mixture. 81 mg of hydroxybenzotriazole, 69 mg of N-ethylmorpholine and 136 mg of dicyclohexylcarbodiimide were added and the mixture was stirred for 64 hours. The mixture was then diluted with ethyl acetate and filtered. The filtrate was washed with aqueous sodium bicarbonate solution and sodium chloride solution. The solvent was removed by evaporation and the residue was chromatographed on silica gel using System G for the elution to give 79 mg of N-[2(R)-hydroxy-4-phenyl-3(S)-[[N-(4-phenylbutyryl)-L-asparaginyl]amino]butyl]-L-proline tert.butyl ester as a white solid: MS: m/e 595 [M+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05446161
出典データセットuspto-grants-1995_08
ORD IDord-a216ced98e744f63b2da24616a360b72
出典メモuspto-grants-1995_08