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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

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참여 물질

역할이름HCID투입량
반응물ChloroformHCID 6212—
반응물2-Fluoro-4-nitrophenolHCID 9825—
반응물Potassium CarbonateHCID 11430—
반응물(R)-(7-Chlorothieno[3,2-b]pyridin-2-yl)(3-(dimethylamino)pyrrolidin-1-yl)methanoneHCID 20745989—
용매Diphenyl EtherHCID 7583—
생성물(R)-(3-(Dimethylamino)pyrrolidin-1-yl)(7-(2-fluoro-4-nitrophenoxy)thieno[3,2-b]pyridin-2-yl)methanoneHCID 5879026471%

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온도190 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08093264B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-4655200704354f03a128a854ccfb2396
출처 메모uspto-grants-2012_01