Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantHexaneHCID 8058—
ReactantChlorosulfonic acidHCID 24638—
ReactantIsobutyramideHCID 68424—
Reactant3-Bromo-1-methyl-4-(1-methyl-1H-indol-3-yl)-1H-pyrrole-2,5-dioneHCID 9818471—
SolventAcetonitrileHCID 6342—
Product2-(1-methyl-1H-indol-3-yl)-3-phenyl-N-methylmaleimideHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06627099B2
Source datasetuspto-grants-2003_09
ORD IDord-bb987a43e59f48e0a2f68bba9e46ebb8
Source noteuspto-grants-2003_09