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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113754Generated: October 25, 2026

1-(5-Amino-1-benzofuran-2-yl)ethanone → 3-[(2-Acetyl-5-benzofuranyl)amino]-1-(2-methoxyethyl)-4-phenyl-1H-pyrrole-2,5-dione

https://huagongshe.com/reaction/2113754

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(5-Amino-1-benzofuran-2-yl)ethanoneHCID 3783367—
Reactant3-Chloro-1-(2-methoxyethyl)-4-phenyl-1H-pyrrole-2,5-dioneHCID 69144282—
SolventAcetonitrileHCID 6342—
Product3-[(2-Acetyl-5-benzofuranyl)amino]-1-(2-methoxyethyl)-4-phenyl-1H-pyrrole-2,5-dioneHCID 1137308317.1%

Reaction Conditions

Temperature150 °C

Reaction Steps

3-Chloro-1-(2-methoxyethyl)-4-phenyl-1H-pyrrole-2,5-dione (0.26 mmol, 70 mg) and 1-(5-aminobenzo[b]furan-2-yl)ethan-1-one (0.53 mmol, 92 mg) was dissolved in dry CH3CN (2 mL) and the reaction mixture was subjected to microwave heating single node 150° C. for 15 min and purified on SiO2 (EtOAc:heptane, 1:1) to give 18 mg (15%) of the title compound. 1H NMR (400 MHz, CDCl3) δ 7.53 (bs, 1H), 7.40 (d, 1H), 7.24-7.09 (m, 5H), 7.06 (dd, 1H), 6.92 (d, 1H), 3.98 (t, J=5.6 Hz, 2H), 3.78 (t, J=5.6 Hz, 2H), 3.52 (s, 3H), 2.69 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07432288B2
Source datasetuspto-grants-2008_10
ORD IDord-4e638a193c954528920253ef6a4030d3
Source noteuspto-grants-2008_10