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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 895161생성일: 2026년 10월 24일

Ammonium → (S)-2-Amino-3-[4-(tert-butoxy)phenyl]propanamide

https://huagongshe.com/ko/reaction/895161

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniumHCID 223—
반응물PyridineHCID 1049—
반응물Di-tert-butyl dicarbonateHCID 90495—
반응물Fmoc-L-Tyr(tBu)-OHHCID 10895791—
용매DichloromethaneHCID 6344—
용매DiethylamineHCID 8021—
용매Ethyl AcetateHCID 8857—
용매1,4-DioxaneHCID 31275—
생성물(S)-2-Amino-3-[4-(tert-butoxy)phenyl]propanamideHCID 1502431781%

반응 단계

N-Fmoc-O-tert-butyl-tyrosine (3.27 g, 7.12 mmol) was dissolved in dioxane (15 mL). Ammonium hydrogenocarbonate (732 mg, 9.26 mmol), di-tert-butyl-dicarbonate (2.02 g, 9.26 mmol) and pyridine (0.4 mL) were added and the mixture was stirred under nitrogen atmosphere at room temperature for 12 h. It was then diluted with ethyl acetate and the organic phase was washed with brine (2×), 5% sulfuric acid (1×) and brine again. It was dried over magnesium sulfate and concentrated. The crude thus obtained (3.17 g) was dissolved in dichloromethane (50 mL) and diethylamine (10 mL). The mixture was stirred at room temperature for 12 h, concentrated under reduced pressure and purified by flash chromatography with DCM/MeOH/NH4OH (95/5/1 then 90/10/1) to give 1.37 g of the desired compound (yield=81%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06914069B2
출처 데이터셋uspto-grants-2005_07
ORD IDord-b15450ccefdb4851b3300913d415f364
출처 메모uspto-grants-2005_07