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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 332642생성일: 2026년 10월 25일

Ammonium formate → (R)-5-(2-Amino-1-(tert-butyldimethylsilyloxy)ethyl)-8-hydroxyquinolin-2(1H)-one formate

https://huagongshe.com/reaction/332642

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참여 물질

역할이름HCID투입량
반응물Ammonium formateHCID 2723923—
반응물(R)-5-(2-Azido-1-((tert-butyldimethylsilyl)oxy)ethyl)-8-(benzyloxy)quinolin-2(1H)-oneHCID 58505233—
촉매PalladiumHCID 23938—
용매MethanolHCID 887—
생성물(R)-5-(2-Amino-1-(tert-butyldimethylsilyloxy)ethyl)-8-hydroxyquinolin-2(1H)-one formateHCID 7109330286%

반응 조건

온도80 °C

반응 단계

Palladium on activated carbon (0.4 g, 10% w/w) was added to a suspension of (R)-5-(2-azido-1-(tert-butyldimethylsilyloxy)ethyl)-8-(benzyloxy)quinolin-2(1H)-one (2.05 g, 4.60 mmol) and ammonium formate (2.87 g, 63 mmol) in methanol (50 mL). The reaction mixture was heated at 80° C. for 1 hour. If after this time, the reaction had not reached completion; the reaction mixture was filtered through celite, washing with methanol. The reaction mixture was concentrated to approximately 50 mL then ammonium formate (2.87 g, 63.0 mmol) and Palladium on activated carbon (0.40 g, 10% w/w) were added. The reaction mixture was heated at 80° C. for 20 minutes, and then filtered through celite, washing with water. The reaction mixture was concentrated under reduced pressure. The resulting solid was washed with water, triturated with ethyl acetate and collected by filtration to afford the title compound (1.32 g, 86%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08877774B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-25fa17234ec7454bab757d93403fc507
출처 메모uspto-grants-2014_11