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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 375276생성일: 2026년 10월 23일

Water → N-tert-butyl-2-(3-azido-2-oxo-5-phenyl-2,3,4,5-tetrahydro-1H-(1)benzazepin-1-yl) ethanoic acid amide

https://huagongshe.com/ko/reaction/375276

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물DimethylformamideHCID 6228—
반응물Sodium AzideHCID 33557—
반응물N-tert-butyl 2-(3-bromo-2-oxo-5-phenyl-2,3,4,5-tetrahydro-1H-(1)benzazepin-1-yl) ethanoic acid amideHCID 15203361—
용매Ethyl AcetateHCID 8857—
생성물N-tert-butyl-2-(3-azido-2-oxo-5-phenyl-2,3,4,5-tetrahydro-1H-(1)benzazepin-1-yl) ethanoic acid amideHCID 15203363—

반응 조건

온도75 °C

반응 단계

To a 250 ml round-bottomed flask equipped with N2 inlet were added N-tert-butyl-2-[3-bromo-2-oxo-5-phenyl-2,3,4,5-tetrahydro-1H-(1)benzazepin-1-yl] ethanoic acid amide, (8.317 g, 19.37 mmoles), 90 ml dimethylformamide (DMF), and sodium azide (5.25 g, 80 mmoles, under nitrogen), and the mixture was heated at 75° C. for 20 hours with stirring. The reaction mixture was then cooled and distributed between water and ethyl acetate, separated, and the aqueous phase was again extracted. The combined extracts were washed with water three times, with bicarbonate solution once, and then dried with brine and sodium sulfate and filtered and evaporated, leaving a gummy residue, 8.58 g (100%), containing some solvent.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05484917
출처 데이터셋uspto-grants-1996_01
ORD IDord-0f850b766acd4aac878515543dd33df7
출처 메모uspto-grants-1996_01