Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 418585생성일: 2026년 10월 25일
Chloroform → (R)-(3-(Dimethylamino)pyrrolidin-1-yl)(7-(2-fluoro-4-nitrophenoxy)thieno[3,2-b]pyridin-2-yl)methanone
https://huagongshe.com/reaction/418585
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Chloroform | HCID 6212 | — |
| 반응물 | 2-Fluoro-4-nitrophenol | HCID 9825 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | (R)-(7-Chlorothieno[3,2-b]pyridin-2-yl)(3-(dimethylamino)pyrrolidin-1-yl)methanone | HCID 20745989 | — |
| 용매 | Diphenyl Ether | HCID 7583 | — |
| 생성물 | (R)-(3-(Dimethylamino)pyrrolidin-1-yl)(7-(2-fluoro-4-nitrophenoxy)thieno[3,2-b]pyridin-2-yl)methanone | HCID 58790264 | 71% |
반응 단계
A mixture of the amide 24 (1.44 g, 4.65 mmol), 2-fluoro-4-nitrophenol (2.21 g, 14.1 mmol) and K2CO3 (2.56 g, 18.5 mmol) in Ph2O (5.0 mL) was heated at 190° C. for 3 hrs. CHCl3 (100 mL) was added to the resultant dark brown mixture and then the mixture was extracted with 1M HCl. The aqueous phase was washed with CHCl3 and basified with NH4OH (pH 11). The resultant cloudy mixture was extracted with CHCl3 and the organic phase was collected, washed with water, dried over anhydrous Na2SO4 then concentrated under reduced pressure. The remaining yellow solid material was purified by flash chromatography, eluent CHCl3/MeOH (95:5, then 80:20) to afford title compound 25 as a white solid (1.41 g, 3.28 mmol, 71% yield). MS (m/z): 431.0 (M+H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08093264B2 |
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| 출처 데이터셋 | uspto-grants-2012_01 |
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| ORD ID | ord-4655200704354f03a128a854ccfb2396 |
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| 출처 메모 | uspto-grants-2012_01 |
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