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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2037005Generated: October 29, 2026

1H-Imidazole-4-carbaldehyde → HCID 178519818, compound

https://huagongshe.com/reaction/2037005

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-Imidazole-4-carbaldehydeHCID 76428—
ReactantHCID 178504622HCID 178504622—
ReactantHCID 178504850HCID 178504850—
SolventIsopropanolHCID 3776—
ProductHCID 178519818HCID 178519818—

Reaction Conditions

Temperature150 °C

Reaction Steps

A mixture of (Z)-5-((4-(cyclopropylamino)-2-(methylsulfinyl)pyrazolo[1,5-a][1,3,5]triazin-8-yl)methylene)imidazolidine-2,4-dione and (Z)-5-((4-(cyclopropylamino)-2-(methylsulfonyl)pyrazolo[1,5-a][1,3,5]triazin-8-yl)methylene)imidazolidine-2,4-dione (20 mg, 0.056 mmol) was mixed with 1H-imidazole-4-carbaldehyde (16 mg, 0.168 mmol) in isopropanol (2 mL). The mixture was stirred under microwave heating at 150° C. for 20 minutes. The reaction mixture was cooled to room temperature and the solvent was removed by rotary evaporation to provide (Z)-1-(4-(cyclopropylamino)-8-((2,5-dioxoimidazolidin-4-ylidene)methyl)pyrazolo[1,5-a][1,3,5]triazin-2-yl)-1H-imidazole-4-carbaldehyde as a crude mixture which was taken on to the next step without further purification. LCMS (ES):>95% pure, m/z 380 [M+H]+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575177B2
Source datasetuspto-grants-2013_11
ORD IDord-8afe6bc4afaf4bd8baf28300bebd2445
Source noteuspto-grants-2013_11