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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 416024Generated: October 25, 2026

Potassium Carbonate → 2-Amino-5-(7-methoxybenzofuran-2-yl)pyrrole-3-carboxamide

https://huagongshe.com/reaction/416024

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantEthanone, 1-(7-methoxy-2-benzofuranyl)-HCID 39378—
ReactantAmidinomalonamide hydrochlorideHCID 3084595—
Reactant2-Bromo-1-(7-methoxy-1-benzofuran-2-yl)ethan-1-oneHCID 82633957—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Product2-Amino-5-(7-methoxybenzofuran-2-yl)pyrrole-3-carboxamideHCID 5829404823%

Reaction Steps

Phenylrimethylammonium tribromide (2.0 g, 5.3 mmol) was added to a solution of 2-acetyl-7-methoxybenzofuran (1.0 g, 5.3 mmol) in anhydrous tetrahydrofuran (25 mL), and the mixture was stirred at room temperature for 4 hours. After the insoluble solid was filtered out, the filtrate was concentrated in vacuo to give a mixture including 2-bromoacetyl-7-methoxybenzofuran. Malonamamidine hydrochloride (1.5 g, 11 mmol) and potassium carbonate (1.5 g, 11 mmol) were added to a solution of this mixture in anhydrous N,N-dimethylformamide (40 mL) and the whole was stirred at 60° C. overnight. After cooling, the reaction mixture was diluted with water (200 mL), and the whole was extracted with ethyl acetate (100 mL, twice). The organic layer was washed with brine (100 mL) and dried over anhydrous magnesium sulfate. The solvent was removed in vacuo, and the obtained residue was purified by silica gel column chromatography to give the title reference compound (0.33 g) as a dark green solid (Yield 23%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088817B2
Source datasetuspto-grants-2012_01
ORD IDord-b322b46377294260b93a1770185f13a0
Source noteuspto-grants-2012_01