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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 84373생성일: 2026년 10월 25일

Sodium Carbonate → 5-(7-(2-Fluoro-4-nitrophenoxy)thieno[3,2-b]pyridin-2-yl)furan-2-carbaldehyde

https://huagongshe.com/reaction/84373

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물5-Formylfuran-2-boronic acidHCID 2734355—
반응물7-(2-Fluoro-4-nitrophenoxy)-2-iodothieno[3,2-b]pyridineHCID 59457661—
촉매HCID 178418476HCID 178418476—
용매Dimethoxyethane ethanol waterHCID 86587095—
생성물5-(7-(2-Fluoro-4-nitrophenoxy)thieno[3,2-b]pyridin-2-yl)furan-2-carbaldehydeHCID 8663518584.2%

반응 조건

온도65 °C

반응 단계

A stirred suspension of 7-(2-fluoro-4-nitrophenoxy)-2-iodothieno[3,2-b]pyridine (24) [US 2006/0287343 A1] (5.00 g, 12.01 mmol, scheme 4)], 5-formyl-2-furanboronic acid (2.19 g, 15.19 mmol), Pd(PPh3)2Cl2 (422 mg, 0.6 mmol), Na2CO3 (8.53 g, 80.50 mmol) in a mixture of DME/ethanol/water (60 mL/40 mL/40 mL) was degassed with nitrogen for 15 min, and heated at 65° C. for five hours under nitrogen. The reaction mixture was allowed to cool to room temperature, and filtered. The cake was successively washed with water and AcOEt. The filtrate and washings were combined, extracted with AcOEt. The extract was successively washed with water, saturated solution of ammonium chloride, water and brine, and concentrated. The residue was combined with the cake, absorbed on silica gel and subjected to flash column chromatography on silica gel (eluents AcOEt/DCM: 10/90 to 20/90, then MeOH/DCM: 5/95) followed by trituration with AcOEt, to afford aldehyde 107 (3.886 g, 84% yield) as a pale clay solid. MS (m/z): 385.0 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846927B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-0d1e0d715cac49d39ed6c7ca02361e41
출처 메모uspto-grants-2014_09