HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1168658Generated: October 25, 2026
Dichloromethane → 2-(1-methyl-1H-indol-3-yl)-3-phenyl-N-methylmaleimide
https://huagongshe.com/reaction/1168658
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Chlorosulfonic acid | HCID 24638 | — |
| Reactant | Isobutyramide | HCID 68424 | — |
| Reactant | 3-Bromo-1-methyl-4-(1-methyl-1H-indol-3-yl)-1H-pyrrole-2,5-dione | HCID 9818471 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-(1-methyl-1H-indol-3-yl)-3-phenyl-N-methylmaleimide | HCID 17843684 | — |
Reaction Steps
Into methylene chloride (83 ml) was dissolved the resultant IM-4 (25 g, 80.5 mmol) obtained as described above, and to this was added dropwise chlorosulfonic acid (8.3 ml) at room temperature. After this mixture was stirred for an hour at room temperature, to the reaction system were added dropwise at a low speed dimethylacetoamide (90 ml)/acetonitrile (45 ml). To this was added dropwise oxy-salt phosphor (15 ml) while being heated and refluxed. After this mixture was heated and refluxed for an hour, hexane (150 ml) was added, then, the mixture was stirred and stood still, and thereafter, the upper layer of hexane was separated and concentrated. The concentrated substances were refined with silica gel column chromatography to obtain 21 g of IM-5.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06627099B2 |
|---|
| Source dataset | uspto-grants-2003_09 |
|---|
| ORD ID | ord-bb987a43e59f48e0a2f68bba9e46ebb8 |
|---|
| Source note | uspto-grants-2003_09 |
|---|