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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1973445Generated: October 25, 2026

Potassium Hydroxide → 3-[2-(2-methyl-5-nitro-1-imidazolyl)ethyl]-2,4-(1H,3H)quinazolinedione

https://huagongshe.com/reaction/1973445

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantQuinazolinedioneHCID 64048—
Reactant1-(2-Hydroxyethyl)-2-methyl-5-nitroimidazole tosylateHCID 86734258—
SolventMethanolHCID 887—
SolventTolueneHCID 1140—
SolventDimethylformamideHCID 6228—
Product3-[2-(2-methyl-5-nitro-1-imidazolyl)ethyl]-2,4-(1H,3H)quinazolinedioneHCID 21491660—

Reaction Steps

A mixture of 15.0 parts of 1-(2-hydroxyethyl)-2-methyl-5-nitroimidazole tosylate and 7.5 parts of 2,4(1H,-3H)-quinazolinedione is dissolved in 190 parts of warm dimethylformamide. 2.9 Parts of potassium hydroxide is dissolved in 80 parts of methanol and diluted with about 95 parts of dimethylformamide. The methanol is removed under reduced pressure, the residual solution added to the quinazolinedione solution, and the resulting mixture heated on a steam bath for 4 hours. The crude solution is cooled, filtered, and diluted with 100 parts of water. The precipitate which forms is separated by filtration and the solvent is evaporated from the filtrate to leave a residue which is stirred with 630 parts of toluene and filtered. The solvent is evaporated from the filtrate to leave a yellow residue. This is dissolved in toluene and dimethylformamide and then concentrated. A precipitate forms and it is separated by filtration to give 3-[2-(2-methyl-5-nitro-1-imidazolyl)ethyl]-2,4-(1H,3H)quinazolinedione melting at about 261°-264° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03997572
Source datasetuspto-grants-1976_12
ORD IDord-964f7b047905449f9f12c37e2028ac04
Source noteuspto-grants-1976_12