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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1657325Generated: November 3, 2026

Tetrahydrofuran → (+)-3,4-dihydro-5-methyl-2-[1-(5-methyl-1-trityl-1H-imidazol-4-yl)ethyl]pyrimido[1,6-a]indol-1(2H)-one

https://huagongshe.com/reaction/1657325

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant3-methyl-2-[2-[[1-(5-methyl-1-trityl-1H-imidazol-4-yl)ethyl]amino]ethyl]indoleHCID 10029785—
SolventEthyl AcetateHCID 8857—
Product(+)-3,4-dihydro-5-methyl-2-[1-(5-methyl-1-trityl-1H-imidazol-4-yl)ethyl]pyrimido[1,6-a]indol-1(2H)-oneHCID 10460239—

Reaction Steps

A mixture of (-)-3-methyl-2-[2-[[1-(5-methyl-1-trityl-1H-imidazol-4-yl)ethyl]amino]ethyl]indole (2.7 g), N,N'-carbonyldiimidazole (2.2 g), 1,8-diazabicyclo[5.4.0]-7-undecene (861 mg) and molecular sieves (810 mg) in dry tetrahydrofuran (40 ml) was stirred at reflux for 2 hours. The reaction mixture was diluted with ethyl acetate, washed with water and brine, dried over anhydrous magnesium sulfate and evaporated in vacuo. The residue was chromatographed over silica gel (eluted with 5% ethyl acetate in chloroform) to give (+)-3,4-dihydro-5-methyl-2-[1-(5-methyl-1-trityl-1H-imidazol-4-yl)ethyl]pyrimido[1,6-a]indol-1(2H)-one (2.09 g) as amorphous powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05256780
Source datasetuspto-grants-1993_10
ORD IDord-1bae87ad33de4776aaf14ff0bb91ce87
Source noteuspto-grants-1993_10