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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 80111Erstellt: 24. Oktober 2026

1,2-Diaminocyclohexane, trans- → 1-Benzothiazol-6-yl-3-(4-chloro-pyridin-3-yl)-imidazolidin-2-one

https://huagongshe.com/de/reaction/80111

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,2-Diaminocyclohexane, trans-HCID 43806—
EduktPotassium Phosphate, TribasicHCID 62657—
Edukt3-Bromo-4-chloropyridineHCID 817696—
Edukt1-Benzothiazol-6-yl-imidazolidin-2-oneHCID 66678554—
KatalysatorCopper iodideHCID 83717—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt1-Benzothiazol-6-yl-3-(4-chloro-pyridin-3-yl)-imidazolidin-2-oneHCID 5963622137,7%

Reaktionsschritte

Using the same reaction conditions as in Example 14, 1-benzothiazol-6-yl-imidazolidin-2-one (I-84b: 0.150 g, 0.684 mmol) was reacted with 3-bromo-4-chloro-pyridine (0.157 g, 0.820 mmol), 1,4-dioxane (20 mL), copper iodide (0.012 g, 0.0684 mmol), trans-1,2-diamino cyclohexane (0.022 g. 0.20 mmol) and potassium phosphate (0.362 g, 1.71 mmol) to afford the crude product. Purification by column chromatography on silica gel (2% MeOH in CHCl3) afforded 85 mg of the product (37.7% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUSRE045173E1
Quelldatensatzuspto-grants-2014_09
ORD IDord-c6448583e65d41efb638aa00cd6f3104
Quellennotizuspto-grants-2014_09