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HRID 16421생성일: 2026년 10월 25일

Ethyl Acetate → Benzenamine,4-[(6-chloro-3-methyl-1h-pyrrolo[2,3-b]pyridin-4-yl)oxy]-3-fluoro-

https://huagongshe.com/reaction/16421

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참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물Potassium CarbonateHCID 11430—
반응물Phenol, 4-amino-2-fluoro-HCID 2735918—
반응물1-acetyl-4,6-dichloro-3-methyl-1H-pyrrolo[2,3-b]pyridineHCID 17979289—
용매Dimethyl SulfoxideHCID 679—
생성물Benzenamine,4-[(6-chloro-3-methyl-1h-pyrrolo[2,3-b]pyridin-4-yl)oxy]-3-fluoro-HCID 17979286—

반응 조건

온도120 °C

반응 단계

300 mg (1.16 mmol) of 1-acetyl-4,6-dichloro-3-methyl-1H-pyrrolo[2,3-b]pyridine (from example XL) and 320 mg (2.32 mmol) of powdered potassium carbonate are suspended in 9 ml of DMSO. The mixture is degassed, and 442 mg (3.48 mmol) of 4-amino-2-fluorophenol are added. The mixture is heated at 120° C. for 4 hours. After addition of ethyl acetate, the mixture is filtered off with suction through CELITE (diatomaceous earth) and the filtercake is washed with ethyl acetate. The filtrate is extracted three times with sat. sodium bicarbonate solution and with sat. sodium chloride solution. The filtrate is dried over sodium sulfate and the solvent is removed under reduced pressure. The residue is purified by column chromatography (silica gel 60, mobile phase: DCM:methanol=50:1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737153B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-f54b7a1f971e4a7496946caf6e8bee25
출처 메모uspto-grants-2010_06