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HRID 84373作成日:2026年10月26日

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

https://huagongshe.com/reaction/84373

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium CarbonateHCID 10340—
反応物5-Formylfuran-2-boronic acidHCID 2734355—
反応物7-(2-Fluoro-4-nitrophenoxy)-2-iodothieno[3,2-b]pyridineHCID 59457661—
触媒HCID 178418476HCID 178418476—
溶媒Dimethoxyethane ethanol waterHCID 86587095—
生成物5-(7-(2-Fluoro-4-nitrophenoxy)thieno[3,2-b]pyridin-2-yl)furan-2-carbaldehydeHCID 8663518584.2%

反応条件

温度65 °C

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846927B2
出典データセットuspto-grants-2014_09
ORD IDord-0d1e0d715cac49d39ed6c7ca02361e41
出典メモuspto-grants-2014_09