Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1850350생성일: 2026년 10월 26일
Triethylamine → 1-{1-[3-(1-Quinolin-2-yl-azetidin-3-yl)-pyrazin-2-yl]-piperidin-4-yl}-ethanone
https://huagongshe.com/reaction/1850350
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 1-(Piperidin-4-yl)ethan-1-one | HCID 2723764 | — |
| 반응물 | 2-(3-(3-Chloropyrazin-2-yl)azetidin-1-yl)quinoline | HCID 58546741 | — |
| 용매 | Dimethyl Sulfoxide | HCID 679 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 1-{1-[3-(1-Quinolin-2-yl-azetidin-3-yl)-pyrazin-2-yl]-piperidin-4-yl}-ethanone | HCID 58547229 | 63% |
반응 단계
To a solution of 2-[3-(3-chloro-pyrazin-2-yl)-azetidin-1-yl]-quinoline (80 mg, 0.27 mmol) and 1-piperidin-4-yl-ethanone (WUXI APPTEC) (34.3 mg, 0.27 mmol) in DMSO (5 mL) was added Et3N (54.5 mg, 0.54 mmol). The reaction mixture was stirred at 100° C. overnight. The reaction mixture was diluted with water, extracted with EtOAc (20 mL×3). The combined organic extracts were washed with water (30 mL) and brine (30 mL), dried over Na2SO4 and filtered. The filtrate was evaporated in vacuo and the residue was purified by flash column chromatography on silica gel to give 1-{1-[3-(1-quinolin-2-yl-azetidin-3-yl)-pyrazin-2-yl]-piperidin-4-yl}-ethanone (65.8 mg, 0.17 mmol, yield 62.9%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08957073B2 |
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| 출처 데이터셋 | uspto-grants-2015_02 |
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| ORD ID | ord-5682078ac7aa4504a7b635e4daa2aa78 |
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| 출처 메모 | uspto-grants-2015_02 |
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