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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710289Generated: November 2, 2026

Maleimide → 4c,7a,7b,12a-Tetrahydro-6H,12H,13H-indeno[2,3-a]pyrrolo[3,4-c]carbazole-5,7-(5H, 7H)dione

https://huagongshe.com/reaction/1710289

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMaleimideHCID 10935—
Reactant2-(2Indenyl)indoleHCID 10585619—
SolventMethanolHCID 887—
Product4c,7a,7b,12a-Tetrahydro-6H,12H,13H-indeno[2,3-a]pyrrolo[3,4-c]carbazole-5,7-(5H, 7H)dioneHCID 1787809962.3%

Reaction Steps

A mixture of 2-(2-indenyl)indole (1.0 g, 4.3 mmol) and maleimide (525 mg, 5.41 mmol) in a 10 cm sealed reaction vial was heated at 180°-190° C. for 30 min. After cooling the reaction to ambient temperature, MeOH (5 mL) was added. The product was collected to give 880 mg (62%) of a white solid product with a m.p. of 254°-255° C. (MeOH). The following NMR data were obtained: 1H NMR (DMSO-d6, 300 MHz): δ3.1-3.4 (m, 2H), 3.8 (m, 2H), 3.95 (t, 1H), 4.35 (d, 1H), 6.9-7.4 (m, 7H), 7.75 (d, 1H), 11.05 (s, 1H), 11.25 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07789610B2
Source datasetuspto-grants-2010_09
ORD IDord-01e57f5a2f2b40a787bfc70657b162c9
Source noteuspto-grants-2010_09