Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 255342생성일: 2026년 10월 25일
2-Hydroxyquinoline-3-carbaldehyde → 7-Fluoro-1-[2-(4-{[(2-oxo-1,2-dihydroquinolin-3-yl)methyl]amino}piperidin-1-yl)ethyl]quinoxalin-2(1H)-one
https://huagongshe.com/reaction/255342
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 2-Hydroxyquinoline-3-carbaldehyde | HCID 589334 | — |
| 반응물 | Sodium triacetoxyborohydride | HCID 5049666 | — |
| 반응물 | 1-(2-(4-aminopiperidin-1-yl)ethyl)-7-fluoroquinoxalin-2(1H)-one | HCID 59397907 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | 7-Fluoro-1-[2-(4-{[(2-oxo-1,2-dihydroquinolin-3-yl)methyl]amino}piperidin-1-yl)ethyl]quinoxalin-2(1H)-one | HCID 15982802 | 35.4% |
반응 단계
A mixture of 1-[2-(4-aminopiperidin-1-yl)ethyl]-7-fluoroquinoxalin-2(1H)-one (Intermediate 140, 130 mg, 0.448 mmol), 2-oxo-1,2-dihydroquinoline-3-carbaldehyde (65 mg, 0.448 mmol) and 3 Å molecular sieves (100 mg) in methanol (6.0 mL) was heated at reflux for 2.5 hours under nitrogen atmosphere. It was cooled to 0° C. and sodium triacetoxy borohydride (189.5 mg, 0.996 mmol) was added and the mixture was allowed to warm to room temperature and stirred overnight. The mixture was filtered and purified through silica gel plug (eluting with 15% methanol in methylene chloride) to give title compound (71 mg).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07875715B2 |
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| 출처 데이터셋 | uspto-grants-2011_01 |
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| ORD ID | ord-9847802978ff4a55817ee19ba6ca6ede |
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| 출처 메모 | uspto-grants-2011_01 |
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