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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1290749Generated: October 28, 2026

Benzaldehyde → 10-benzylidene-5H,10H-imidazo[1,2-a]indeno-[1,2-e]pyrazin-4-one

https://huagongshe.com/reaction/1290749

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
Reactant5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazin-4-oneHCID 10353549—
CatalystTetrabutylammonium BromideHCID 74236—
SolventAcetic AcidHCID 176—
SolventDimethyl SulfoxideHCID 679—
Product10-benzylidene-5H,10H-imidazo[1,2-a]indeno-[1,2-e]pyrazin-4-oneHCID 703438841.6%

Reaction Conditions

Temperature20 °C

Reaction Steps

A suspension of 5.75 g of 5H,10H-imidazo-[1,2-a]indeno[1,2-e]pyrazin-4-one, 10 g of sodium hydroxide pellets and 125 mg of tetrabutylammonium bromide in 200 ml of dimethyl sulphoxide is stirred at a temperature in the region of 20° C. 3.18 g of benzaldehyde are then added and the stirring is continued for 18 hours at a temperature in the region of 20° C. The reaction mixture is poured into a mixture of water and ice (250 ml) and acidified with 100 ml of acetic acid. The solid formed is filtered off and the crude product is purified by two successive chromatographies on a column of silica with a mixture of dichloromethane and methanol (90/10 by volume). 0.13 g of 10-benzylidene-5H,10H-imidazo[1,2-a]indeno-[1,2-e]pyrazin-4-one is thus obtained, in the form of a yellow solid melting above 260° C. (Analysis % calculated C: 77.16, H: 4.21, N: 13.50, O: 5.14, % found C: 76.7, H: 3.7, N: 13.2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05753657
Source datasetuspto-grants-1998_05
ORD IDord-dde683bbfa194685896c70993f11c00e
Source noteuspto-grants-1998_05