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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 863695Generated: October 26, 2026

Triethylamine → 3-[7,8,9,10-tetrahydro-6H-azepino[1,2-a]indol-11-yl]-3-(1-methyl-3-indolyl)furan-2,5-dione

https://huagongshe.com/reaction/863695

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant2-(1-methyl-1H-indol-3-yl)acetic acidHCID 254166—
ReactantHCID 11116734HCID 11116734—
SolventDichloromethaneHCID 6344—
Product3-[7,8,9,10-tetrahydro-6H-azepino[1,2-a]indol-11-yl]-3-(1-methyl-3-indolyl)furan-2,5-dioneHCID 1969631622.5%

Reaction Steps

1.5 g of oxalyl chloride were added dropwise to an ice-cold solution of 2.0 g of 7,8,9,10-tetrahydro-6H-azepino[1,2-a]indole (J. Org. Chem. 33, 1968, 4286) in 50 ml of dichloromethane. The mixture was stirred for 2 hours. The solvent was removed in a vacuum and the residue was dissolved in dichloromethane. The solution obtained was added to a solution of 2.2 g of 1-methyl-3-indolylacetic acid and 2.73 g of triethylamine in 50 ml of dichloromethane. The mixture was stirred and then concentrated. The residue was chromatographed on silica gel with dichloromethane and there was obtained 1.0 g of 3-[7,8,9,10-tetrahydro-6H-azepino[1,2-a]indol-11-yl]-3-(1-methyl-3-indolyl)furan-2,5-dione of melting point 257°-259° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05721245
Source datasetuspto-grants-1998_02
ORD IDord-b40e585f1f6b4f499d8db2815a94f907
Source noteuspto-grants-1998_02