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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1820890생성일: 2026년 10월 26일

alpha-Chloro-m-nitrotoluene → 3-(3,4-Dimethoxy-phenyl)-1-(3-nitro-benzyl)-1H-pyrrolo[2,3-b]pyridine

https://huagongshe.com/reaction/1820890

반응식

참여 물질

역할이름HCID투입량
반응물alpha-Chloro-m-nitrotolueneHCID 12078—
반응물Sodium hydrideHCID 24758—
반응물3-(3,4-dimethoxy-phenyl)-1H-pyrrolo[2,3-b]pyridineHCID 11673285—
용매DimethylformamideHCID 6228—
생성물3-(3,4-Dimethoxy-phenyl)-1-(3-nitro-benzyl)-1H-pyrrolo[2,3-b]pyridineHCID 5789175477%

반응 단계

3-(3,4-Dimethoxy-phenyl)-1H-pyrrolo[2,3-b]pyridine 1 (35 mg, 0.14 mmole) was dissolved in 15 mL of DMF and sodium hydride (60% dispersion in mineral oil, 10 mg, 0.25 mmol) was added in small portion to the reaction mixture. After stirring for 30 minutes, m-nitro-benzyl chloride (30 mg, 0.14 mmole) was added to the reaction mixture and was stirred for 2 hours. The reaction mixture was poured into 50 mL of ice water and was extracted with ethyl acetate. The organic layer was washed with saturated sodium bicarbonate followed by saturated potassium bisulfate 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 in hexanes) to yield 42 mg (71%) of the titled compound as a white solid. MS(ESI) [M+H+]+=390.1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07605168B2
출처 데이터셋uspto-grants-2009_10
ORD IDord-4ff113348dd74e3cac51b3bad10beb82
출처 메모uspto-grants-2009_10