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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 224767생성일: 2026년 10월 24일

Triethylamine → N-Acetylphenylalanylarginine ethyl ester

https://huagongshe.com/ko/reaction/224767

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물DicyclohexylcarbodiimideHCID 10868—
반응물N-Acetyl-L-phenylalanineHCID 74839—
반응물N-HydroxysuccinimideHCID 80170—
반응물HCID 178472568HCID 178472568—
용매DimethylformamideHCID 6228—
생성물N-Acetylphenylalanylarginine ethyl esterHCID 194320—

반응 조건

온도-15 °C

반응 단계

0.829 g (4 mmols) of N-acetyl-L-phenylalanine are dissolved in 40 ml of dimethylformamide. 1.10 g (4 mmols) of finely powdered L-arginine ethyl ester dihydrochloride, 0.56 ml (4 mmols) of triethylamine and 0.69 g (6 mmols) of N-hydroxysuccinimide are added and the mixture is cooled to -15° C. After adding 0.91 g (4.4 mmols) of dicyclohexylcarbodiimide, the mixture is stirred at -5° C. for 7 hours, at 5° C. overnight and at room temperature for 5 hours. The precipitate is filtered off and the solution is concentrated almost to dryness in vacuo on a rotary evaporator. After taking up the residue in 80 ml of water, the pH of the solution is adjusted to 6.0 with triethylamine and the solution is discharged onto a column (1.5×40 cm) of Cm- "Sephadex" (Trade Mark) C-25, equilibrated with 0.05 M triethylammonium acetate of pH 6.0. Elution is carried out with a linear gradient increasing to 0.2 M triethylammonium acetate of pH 6.0 (720 ml; 50 ml/hour; size of fraction: 8 ml). Fractions 75-110, which, according to spotting on filter paper and spraying with Sakaguchi reagent, contains most of the eluted material, is lyophilised. 0.5 ml of ethanol is added to the combined residues and the product is precipitated with 60 ml of ethyl acetate. The precipitate is dried over phosphorus pentoxide in a desiccator.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04234477
출처 데이터셋uspto-grants-1980_11
ORD IDord-f80a15044f8b4063a1529cd727d31643
출처 메모uspto-grants-1980_11