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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 80225Erstellt: 23. Oktober 2026

1,2-Diaminocyclohexane → 1-Benzothiazol-6-yl-3-pyridin-3-yl-4-trifluoromethyl-imidazolidin-2-one

https://huagongshe.com/de/reaction/80225

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,2-DiaminocyclohexaneHCID 4610—
Edukt3-BromopyridineHCID 12286—
EduktPotassium Phosphate, TribasicHCID 62657—
Edukt1-Benzothiazol-6-yl-4-trifluoromethyl-imidazolidin-2-oneHCID 68787913—
KatalysatorCopper iodideHCID 83717—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt1-Benzothiazol-6-yl-3-pyridin-3-yl-4-trifluoromethyl-imidazolidin-2-oneHCID 4987264923,8%

Reaktionsschritte

Using the same reaction conditions and work up as described in example 1, step-3,1-Benzothiazol-6-yl-4-trifluoromethyl-imidazolidin-2-one (I-170b: 50 mg, 0.174 mmol) was refluxed with 3-Bromo-pyridine (33 mg, 0.209 mmol), copper iodide (3.3 mg, 0.0174 mmol), Cyclohexane-1,2-diamine (6 mg, 0.0522 mmol), potassium phosphate (110 mg, 0.522 mmol) and 1,4-Dioxane (2 mL) at 120° C. for 12 hours to afford the crude product. Purification by column chromatography on silica gel (2% methanol in chloroform) followed by n-pentane washing afforded 15 mg of the product (23.8% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUSRE045173E1
Quelldatensatzuspto-grants-2014_09
ORD IDord-10082d1ae133471d889e5801d44f73b2
Quellennotizuspto-grants-2014_09