HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bisindolylmaleimide V → HCID 496503, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bisindolylmaleimide V | HCID 2400 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 496503 | HCID 496503 | 93.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06589977B1 |
| Source dataset | uspto-grants-2003_07 |
| ORD ID | ord-31d1774ff88d48b8b3f8d5fb9b3d6036 |
| Source note | uspto-grants-2003_07 |