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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 40721생성일: 2026년 10월 24일

Dimethylformamide → 5-fluoro-2-[1-(4-methoxy-benzyl)-1H-pyrrolo[2,3-b]pyridin-5-yl]-oxazolo[5,4-b]pyridine

https://huagongshe.com/ko/reaction/40721

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Potassium CarbonateHCID 11430—
반응물2,6-Difluoropyridin-3-amineHCID 45080006—
반응물1-(4-Methoxybenzyl)-1H-pyrrolo[2,3-b]pyridine-5-carboxylic acidHCID 58220162—
용매PyridineHCID 1049—
용매DichloromethaneHCID 6344—
생성물5-fluoro-2-[1-(4-methoxy-benzyl)-1H-pyrrolo[2,3-b]pyridin-5-yl]-oxazolo[5,4-b]pyridineHCID 58220157—

반응 조건

온도150 °C

반응 단계

To a stirred solution of 1-(4-methoxy-benzyl)-1H-pyrrolo[2,3-b]pyridine-5-carboxylic acid (47 mg, 0.17 mmol) in CH2Cl2 (2 mL) was added 1-chloro-N,N-2-trimethylpropenylamine (45 μL, 0.34 mmol). Following formation of the resulting acid chloride, the reaction mixture was concentrated affording a residue that was dissolved in pyridine (2 mL) before 2,6-difluoro-pyridin-3-ylamine (20 mg, 0.15 mmol) was added in one portion. After an additional 30 minutes the reaction mixture was concentrated to dryness affording a residue, to which was added DMF (2 mL) and K2CO3 (64 mg, 0.46 mmol). The resulting mixture was heated by microwave to 150° C. for 10 min, after which the resulting mixture was filtered and concentrated, affording 5-fluoro-2-[1-(4-methoxy-benzyl)-1H-pyrrolo[2,3-b]pyridin-5-yl]-oxazolo[5,4-b]pyridine as a crude residue which was subsequently used without further purification. ES MS (M+H+)=375.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08530483B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-36b9a2fd13594de196727a03f2237ade
출처 메모uspto-grants-2013_09