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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1820889생성일: 2026년 10월 27일

Sodium hydride → [3-(3,4-Dimethoxy-phenyl)-pyrrolo[2,3-b]pyridin-1-yl]-(2-ethoxy-naphthalen-1-yl)-methanone

https://huagongshe.com/reaction/1820889

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물1-Naphthalenecarbonyl chloride, 2-ethoxy-HCID 108679—
반응물3-(3,4-dimethoxy-phenyl)-1H-pyrrolo[2,3-b]pyridineHCID 11673285—
용매DimethylformamideHCID 6228—
생성물[3-(3,4-Dimethoxy-phenyl)-pyrrolo[2,3-b]pyridin-1-yl]-(2-ethoxy-naphthalen-1-yl)-methanoneHCID 1158328570.4%

반응 단계

3-(3,4-Dimethoxy-phenyl)-1H-pyrrolo[2,3-b]pyridine 1 (638 mg, 2.51 mmole) was dissolved in DMF (30 mL) and sodium hydride (60% dispersion in mineral oil, 100 mg, 2.50 mmole) was added in small portions to the reaction mixture. After stirring for 30 minutes, 2-ethoxy-1-naphthoyl chloride (646 mg, 2.76 mmole) was added and the reaction was stirred for 4 hours. The reaction mixture was poured into 200 mL of ice water and was extracted with ethyl acetate. The organic layer was washed with saturated bicarbonate solution followed by saturated potassium hydrogen sulfate and then brine. The resulting solution was dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The residue was purified by silica gel chromatography (30% ethyl acetate:hexanes) to yield 800 mg (70%) of the titled compound as a white solid MS(ESI) [M+H+]+=453.06.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07605168B2
출처 데이터셋uspto-grants-2009_10
ORD IDord-57c9ad57aeee40adb993f07128b8d86d
출처 메모uspto-grants-2009_10