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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1290745Generated: October 31, 2026

1,4-Dibromobutane → 5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazine

https://huagongshe.com/reaction/1290745

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DibromobutaneHCID 8056—
ReactantSodium HydroxideHCID 14798—
Reactant5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazin-4-oneHCID 10353549—
CatalystTetrabutylammonium BromideHCID 74236—
SolventDimethyl SulfoxideHCID 679—
Product5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazineHCID 131720656—

Reaction Steps

The procedure is performed as in Example 9, but starting with 1.1 g of 5H,10H-imidazo[1,2-a]indeno-[1,2-e]pyrazin-4-one, 40 ml of dimethyl sulphoxide, 2 g of sodium hydroxide pellets, 32 mg of tetrabutylammonium bromide and 0.6 ml of 1,4-dibromobutane. After drying at 80° C., 0.17 g of spiro[5H,10H-imidazo[1,2-a]indeno[l,2-e]pyrazine-10:1'-cyclopentane]-4-one is obtained, in the form of a white solid melting above 260° C. (Analysis % calculated C: 73.63, H: 5.45, N: 15.15, O: 5.77, % found C: 73.8, H: 5.8, N: 15.1, O: 6.0).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05753657
Source datasetuspto-grants-1998_05
ORD IDord-dbf8d9ad7a874a66bfbc50ff6bbc3020
Source noteuspto-grants-1998_05