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HRID 16417생성일: 2026년 10월 25일

Potassium Carbonate → 4-[(6-Chloro-1H-pyrrolo[2,3-b]pyridin-4-yl)oxy]-3-fluoroaniline

https://huagongshe.com/reaction/16417

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Phenol, 4-amino-2-fluoro-HCID 2735918—
반응물6-chloro-4-nitro-1H-pyrrolo[2,3-b]pyridineHCID 17979338—
반응물Potassium tert-butoxideHCID 23665647—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물4-[(6-Chloro-1H-pyrrolo[2,3-b]pyridin-4-yl)oxy]-3-fluoroanilineHCID 17979284—

반응 단계

4-Amino-2-fluorophenol (0.77 g, 6.07 mmol) is dissolved in DMF. Potassium tert-butoxide (0.68 g, 6.07 mmol) is added, and the mixture is stirred at room temperature for 30 minutes. Powdered potassium carbonate (0.35 g, 2.53 mmol) and 1 g (5.06 mmol) of 6-chloro-4-nitro-1H-pyrrolo[2,3-b]pyridine (from example XXX) are then added successively. The mixture is stirred at 120° C. for 12 hours. After cooling, the mixture is diluted with ethyl acetate (200 ml). The suspension is filtered off with suction through Celite®, and the filtercake is washed with ethyl acetate. The solution is extracted successively with aqueous sodium bicarbonate solution and sodium chloride solution. The organic phase is dried over anhydrous magnesium sulfate and concentrated. The residue is purified by column chromatography (silica gel 60, mobile phase: DCM:acetone=5:1). This gives 0.95 g (67% of theory) of product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737153B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-ea0e983032304f259c08a3a0dfb9a679
출처 메모uspto-grants-2010_06