돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 4981생성일: 2026년 10월 24일

Hydrochloric Acid → Ac-Ala-Lys(Boc)-OH

https://huagongshe.com/ko/reaction/4981

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물TriethylamineHCID 8471—
반응물Sodium HydroxideHCID 14798—
반응물N-HydroxysuccinimideHCID 80170—
반응물N-Acetyl-L-alanineHCID 88064—
반응물(2S)-2-amino-6-(((tert-butoxy)carbonyl)amino)hexanoic acidHCID 2733283—
용매1,4-DioxaneHCID 31275—
생성물Ac-Ala-Lys(Boc)-OHHCID 131717743—

반응 단계

Ac-Ala-Lys(Boc)-OH was prepared by coupling the N-hydroxysuccinimide ester of Ac-Ala-OH, prepared by the method of Anderson et al., J. Am. Chem. Soc. 86: 1839, (1964), to H-Lys(Boc)-OH. The N-hydroxy-succinimide of Ac-Ala-OH (6.25 g, 27.4 mmoles) was dissolved in 30 mL of dioxane and was added to a solution of H-Lys(Boc)-OH (7.50 g, 30.4 mmoles) dissolved in a solution consisting of 30 mL of 1.0N sodium hydroxide and triethylamine (2.12 mL, 15.0 mmoles). The reaction mixture was stirred overnight, then acidified with hydrochloric acid. Sufficient dry sodium chloride to nearly saturate the solution was added. The product was extracted into ethyl acetate and it was washed with 0.2N hydrochloric acid prepared in saturated aqueous sodium chloride. The organic phase was dried over anhydrous sodium sulfate and filtered. Solvent was removed by evaporation. The product was crystallized from ethyl acetate:hexane to yield 7.3 g (mp 86°-89°).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05242904
출처 데이터셋uspto-grants-1993_09
ORD IDord-408c8484fe124834b5520e846e9adf68
출처 메모uspto-grants-1993_09