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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 481453Generated: October 25, 2026

Sodium Hydroxide → 8-(3-carboxymethylureido)-5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazine-4-one dihydrate

https://huagongshe.com/reaction/481453

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant8-(3-ethoxycarbonylmethylureido)-5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazine-4-oneHCID 19066033—
SolventEthanolHCID 702—
Product8-(3-carboxymethylureido)-5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazine-4-one dihydrateHCID 19065995—

Reaction Conditions

Temperature20 °C

Reaction Steps

20 ml of 30% sodium hydroxide solution are added, at a temperature in the region of 20° C., to 1 g of 8-(3-ethoxycarbonylmethylureido)-5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazine-4-one in suspension in 40 ml of ethanol. The reaction is continued for 18 hours at 50° C. After cooling to a temperature in the region of 20° C., the precipitate formed is filtered, then taken up in 20 ml of distilled water and the mixture is acidified using concentrated hydrochloric acid. The suspension is stirred for 2 hours at a temperature in the region of 20° C. and then filtered, washed with water and dried under partial vacuum (1 mm Hg, 0.13 kPa) at 100° C. After recrystallization from dimethylformamide, there is obtained 0.22 g of 8-(3-carboxymethylureido)-5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazine-4-one dihydrate in the form of a beige solid, the melting point of which is greater than 260° C. (Analysis C16H12N5O4 2.0.H2O.0.1DMF, % calculated C: 56.64, H: 3.86, N: 20.64, % found C: 56.7, H: 3.8, N: 21.0).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05789406
Source datasetuspto-grants-1998_08
ORD IDord-87c0dac94bfe4e5998e96841c3e564a9
Source noteuspto-grants-1998_08