Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1357091Generated: November 1, 2026

Bisindolylmaleimide V → HCID 496503, compound

https://huagongshe.com/reaction/1357091

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBisindolylmaleimide VHCID 2400—
CatalystHCID 178418390HCID 178418390—
SolventDimethylformamideHCID 6228—
ProductHCID 496503HCID 49650393.9%

Reaction Steps

To a solution of 2,3-bis(1H-indol-3-yl)-N-methylmaleimide (14 mg, 0.04 mmol) synthesized according to a known method (Tetrahedron, Vol. 44, p. 2887, 1988) in DMF (1 mL) was added a small amount of 10% palladium-carbon and the whole was stirred at room temperature for 1 day under hydrogen atmosphere. The palladium-carbon was removed by filtration, and the filtrate was concentrated under reduced pressure. The residue was purified by column chromatography over silica gel (ethyl acetate:n-hexane=2:1) to obtain 3,4-bis(1H-indol-3-yl)-1-methy-2,5-dioxopyrrolidine (12.9 mg, 91.7%) as a mixture of two isomers (A:B=2.7:1.0) as pale red solids.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06589977B1
Source datasetuspto-grants-2003_07
ORD IDord-31d1774ff88d48b8b3f8d5fb9b3d6036
Source noteuspto-grants-2003_07