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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 80040Erstellt: 23. Oktober 2026

1,2-Diaminocyclohexane, trans- → 1-(4-Methyl-pyridin-3-yl)-3-(5-methyl-thiophen-2-yl)-imidazolidin-2-one

https://huagongshe.com/de/reaction/80040

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,2-Diaminocyclohexane, trans-HCID 43806—
EduktPotassium Phosphate, TribasicHCID 62657—
Edukt2-Bromo-5-methylthiopheneHCID 69831—
Edukt1-(4-Methylpyridin-3-yl)imidazolidin-2-oneHCID 59636170—
KatalysatorCopper iodideHCID 83717—
LösungsmittelMethanolHCID 887—
LösungsmittelChloroformHCID 6212—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt1-(4-Methyl-pyridin-3-yl)-3-(5-methyl-thiophen-2-yl)-imidazolidin-2-oneHCID 4987186774%

Reaktionsbedingungen

Temperatur110 °C

Reaktionsschritte

Copper iodide (16 mg, 0.084 mmol), trans-1,2-diamino cyclohexane (28.8 mg, 0.25 mmol) and potassium phosphate (445 mg, 2.1 mmol) were added to 1,4-Dioxane (10 mL) previously degassed with argon (10 minutes). The reaction mixture was purged with argon for a further 10 minutes, followed by the addition of 1-(4-methyl-pyridin-3-yl)-imidazolidin-2-one (I-14b: 150 mg, 0.84 mmol) and 2-bromo-5-methylthiophene (150 mg, 0.84 mmol). The resulting mixture was heated to reflux at 110° C. for 4 hours. The reaction was monitored by TLC (10% MeOH in chloroform). The reaction mixture was filtered through celite and the celitebed was washed with chloroform. The organic layer was dried over Na2SO4 and concentrated. The concentrate was quenched with ice, the precipitate formed was collected and dried to afford 170 mg (74% yield) of 1-(4-methyl-pyridin-3-yl)-3-(5-methyl-thiophen-2-yl)-imidazolidin-2-one.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUSRE045173E1
Quelldatensatzuspto-grants-2014_09
ORD IDord-9d155cf1125b484f9d5ab50ed4b67e28
Quellennotizuspto-grants-2014_09