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HRID 1820890作成日:2026年10月27日

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

https://huagongshe.com/reaction/1820890

反応式

関与物質

役割名称HCID仕込み量
反応物alpha-Chloro-m-nitrotolueneHCID 12078—
反応物Sodium hydrideHCID 24758—
反応物3-(3,4-dimethoxy-phenyl)-1H-pyrrolo[2,3-b]pyridineHCID 11673285—
溶媒DimethylformamideHCID 6228—
生成物3-(3,4-Dimethoxy-phenyl)-1-(3-nitro-benzyl)-1H-pyrrolo[2,3-b]pyridineHCID 5789175477%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07605168B2
出典データセットuspto-grants-2009_10
ORD IDord-4ff113348dd74e3cac51b3bad10beb82
出典メモuspto-grants-2009_10