Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethyl Acetate | HCID 8857 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | Phenol, 4-amino-2-fluoro- | HCID 2735918 | — |
| 반응물 | 1-acetyl-4,6-dichloro-3-methyl-1H-pyrrolo[2,3-b]pyridine | HCID 17979289 | — |
| 용매 | Dimethyl Sulfoxide | HCID 679 | — |
| 생성물 | Benzenamine,4-[(6-chloro-3-methyl-1h-pyrrolo[2,3-b]pyridin-4-yl)oxy]-3-fluoro- | HCID 17979286 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07737153B2 |
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| 출처 데이터셋 | uspto-grants-2010_06 |
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| ORD ID | ord-f54b7a1f971e4a7496946caf6e8bee25 |
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| 출처 메모 | uspto-grants-2010_06 |
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