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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1757718생성일: 2026년 10월 23일

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/ko/reaction/1757718

반응식

참여 물질

역할이름HCID투입량
반응물4-Phenylbutyric AcidHCID 4775—
반응물EthylmorpholineHCID 7525—
반응물DicyclohexylcarbodiimideHCID 10868—
반응물N-[3(S)-[[L-asparaginyl]amino]-2(R)-hydroxy-4-phenylbutyl]-L-proline tert.butyl esterHCID 70041604—
반응물HCID 178418300HCID 178418300—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물N-[2(R)-hydroxy-4-phenyl-3(S)-[[N-(4-phenylbutyryl)-L-asparaginyl]amino]butyl]-L-proline tert.butyl esterHCID 7004365722.3%

반응 단계

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]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05446161
출처 데이터셋uspto-grants-1995_08
ORD IDord-a216ced98e744f63b2da24616a360b72
출처 메모uspto-grants-1995_08