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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ammonium formate | HCID 2723923 | — |
| 반응물 | (R)-5-(2-Azido-1-((tert-butyldimethylsilyl)oxy)ethyl)-8-(benzyloxy)quinolin-2(1H)-one | HCID 58505233 | — |
| 촉매 | Palladium | HCID 23938 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | (R)-5-(2-Amino-1-(tert-butyldimethylsilyloxy)ethyl)-8-hydroxyquinolin-2(1H)-one formate | HCID 71093302 | 86% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08877774B2 |
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| 출처 데이터셋 | uspto-grants-2014_11 |
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| ORD ID | ord-25fa17234ec7454bab757d93403fc507 |
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| 출처 메모 | uspto-grants-2014_11 |
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