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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 80138Erstellt: 24. Oktober 2026

1,2-Diaminocyclohexane, trans- → 1-Benzo[b]thiophen-3-yl-3-(4-methyl-pyridin-3-yl)-imidazolidin-2-one

https://huagongshe.com/de/reaction/80138

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,2-Diaminocyclohexane, trans-HCID 43806—
EduktPotassium Phosphate, TribasicHCID 62657—
EduktBenzo(b)thiophene, 3-bromo-HCID 123250—
Edukt1-(4-Methylpyridin-3-yl)imidazolidin-2-oneHCID 59636170—
KatalysatorCopper iodideHCID 83717—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt1-Benzo[b]thiophen-3-yl-3-(4-methyl-pyridin-3-yl)-imidazolidin-2-oneHCID 5963619636,3%

Reaktionsschritte

Using the same reaction conditions as in Example 14, 1-(4-methyl-pyridin-3-yl)-imidazolidin-2-one (I-14b: 150 mg, 0.8465 mmol) was reacted with 3-bromo-benzo[b]thiophene (216.3 mg, 1.0158 mmol), 1,4-dioxane (50 mL), copper iodide (10.7 mg, 0.0865 mmol), trans-1,2-diamino cyclohexane (29 mg, 0.2539 mmol) and potassium phosphate (449.1 mg, 2.1162 mmol) to afford the crude product. Purification by column chromatography on silica gel (2% MeOH in CHCl3) afforded 95 mg of the product (36.3% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUSRE045173E1
Quelldatensatzuspto-grants-2014_09
ORD IDord-71e8f838646346b5bee2ddc11d390c65
Quellennotizuspto-grants-2014_09