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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 875152생성일: 2026년 10월 24일

Morpholine → tert-butoxycarbonyl-(1S)-1-methyl-2-morpholin-4-yl-2-oxo-1-phenylethylamine

https://huagongshe.com/ko/reaction/875152

반응식

참여 물질

역할이름HCID투입량
반응물MorpholineHCID 8083—
반응물DiisopropylethylamineHCID 81531—
반응물O-benzotriazol-1-yl-tetramethyluroniumHCID 130500—
반응물(S)-2-(Boc-amino)-2-phenylpropanoic acidHCID 13678038—
용매DimethylformamideHCID 6228—
생성물tert-butoxycarbonyl-(1S)-1-methyl-2-morpholin-4-yl-2-oxo-1-phenylethylamineHCID 5744416588%

반응 단계

630 mg (2.374 mmol) of N-(tert-butoxycarbonyl)-2-phenyl-D-alanine were dissolved in 20 mL of dry DMF and O-(benzotriazol-1-yl)-1,1,3,3-tetramethyluronium tetrafluoborate (TBTU, 1.37 g, 4.27 mmol), morpholine (0.412 mL, 4.73 mmol) and diisopropylethylamine (1.63 mL, 9.5 mol) were added. The mixture was stirred at room temperature for 1 hour, then the solvent was removed and the residue dissolved with dichloromethane. The solution was washed with saturated NaHCO3, brine, water and dried over Na2SO4. 700 mg of the title compound were recovered (88% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08981089B2
출처 데이터셋uspto-grants-2015_03
ORD IDord-c2fc58b057564997847ea5cd4f374881
출처 메모uspto-grants-2015_03