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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 584835Generated: October 26, 2026

1,2-Dimethoxyethane → 1-(1-Ethylpropyl)-6-mesityl-4-methyl-1H-pyrrolo[3,2-c]quinoline

https://huagongshe.com/reaction/584835

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantBarium hydroxide, octahydrateHCID 17749109—
ReactantMesitylboric acidHCID 22237855—
Reactant1-(1-Ethylpropyl)-6-iodo-4-methyl-1H-pyrrolo[3,2-c]quinolineHCID 22249594—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Product1-(1-Ethylpropyl)-6-mesityl-4-methyl-1H-pyrrolo[3,2-c]quinolineHCID 222499886.7%

Reaction Conditions

Temperature80 °C

Reaction Steps

1-(1-Ethylpropyl)-6-iodo-4-methyl-1H-pyrrolo[3,2-c]quinoline (170 mg, 0.45 mmol), mesitylboric acid (82 mg, 0.50 mmol), barium hydroxide octahydrate (213 mg, 0.68 mmol) and tetrakistriphenylphosphinepalladium (26 mg, 0.02 mmol) were suspended into a mixture of 1,2-dimethoxyethane (6 mL) and water (1 mL), followed by stirring at 80° C. overnight in nitrogen atmosphere. Water was added to the reaction mixture, followed by extracting with ethyl acetate. The organic layer was washed with water and brine, dried over anhydrous magnesium sulfate, and then evaporated. The residue was purified by silica gel column chromatography (5% ethyl acetate/hexane), to give the title compound (11 mg, 0.03 mmol) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06927221B2
Source datasetuspto-grants-2005_08
ORD IDord-060bf3a12233496f90b38eae4a287891
Source noteuspto-grants-2005_08