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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1521685생성일: 2026년 10월 24일

Methyl 3-({3-[(tert-butoxycarbonyl)amino]propyl}amino)-4-nitrobenzoate → Methyl 4-amino-3-({3-[(tert-butoxycarbonyl)amino]propyl}amino)benzoate

https://huagongshe.com/ko/reaction/1521685

반응식

참여 물질

역할이름HCID투입량
반응물Methyl 3-({3-[(tert-butoxycarbonyl)amino]propyl}amino)-4-nitrobenzoateHCID 67235341—
촉매PalladiumHCID 23938—
용매Ethyl AcetateHCID 8857—
생성물Methyl 4-amino-3-({3-[(tert-butoxycarbonyl)amino]propyl}amino)benzoateHCID 1196207780%

반응 단계

A stirred suspension of methyl 3-({3-[(tert-butoxycarbonyl)amino]propyl}amino)-4-nitrobenzoate (6.5 g, 18.4 mmol) in ethyl acetate (500 mL) is hydrogenated over 10% palladium on carbon (2.6 g) under balloon pressure for 4 h. The catalyst is removed by filtration through Celite, washing well with ethyl acetate. The solvent is evaporated to afford the title compound (4.72 g, 80%) as a white solid. LCMS (Method T) 1.39 min, 324.70 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09073926B2
출처 데이터셋uspto-grants-2015_07
ORD IDord-643ca5a2ebb147999dd8196d19ffdd6f
출처 메모uspto-grants-2015_07