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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1820890Generated: October 25, 2026

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

https://huagongshe.com/reaction/1820890

Reaction equation

Participants

RoleNameHCIDCharge
Reactantalpha-Chloro-m-nitrotolueneHCID 12078—
ReactantSodium hydrideHCID 24758—
Reactant3-(3,4-dimethoxy-phenyl)-1H-pyrrolo[2,3-b]pyridineHCID 11673285—
SolventDimethylformamideHCID 6228—
Product3-(3,4-Dimethoxy-phenyl)-1-(3-nitro-benzyl)-1H-pyrrolo[2,3-b]pyridineHCID 5789175477%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07605168B2
Source datasetuspto-grants-2009_10
ORD IDord-4ff113348dd74e3cac51b3bad10beb82
Source noteuspto-grants-2009_10