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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1357108Generated: November 3, 2026

Water → 1-benzyl-3,4-bis(1H-indol-3-yl)pyrrole-2,5-dione

https://huagongshe.com/reaction/1357108

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzylamineHCID 7504—
Reactant2,5-Furandione, 3,4-di-1H-indol-3-yl-HCID 5327652—
SolventDimethylformamideHCID 6228—
Product1-benzyl-3,4-bis(1H-indol-3-yl)pyrrole-2,5-dioneHCID 1136206887.8%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 2,3-bis(1H-indol-3-yl)maleic anhydride (100 mg, 0.3 mmol) synthesized according to a known method (Tetrahedron, Vol. 44, p. 2887, 1988) and dissolved in DMF (10 mL) and water (10 mL) was added benzylamine (0.13 mL, 1.2 mmol), and the whole was stirred at 100 ° C. for 2 hours. The reaction mixture was concentrated under reduced pressure to remove DMF, and the concentrate was extracted with ethyl acetate. The extract was washed with water, dried over sodium sulfate, and then concentrated under reduced pressure. The residue was purified by column chromatography over silica gel (ethyl acetate:n-hexane=2:1) to obtain 2,3-bis(1H-indol-3-yl)-N-benzylmaleimide (110 mg, 86.6%) as red solids.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06589977B1
Source datasetuspto-grants-2003_07
ORD IDord-f0d565ac727a4dc78f6e33dfaf5de99d
Source noteuspto-grants-2003_07