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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 711180Erstellt: 26. Oktober 2026

Potassium Carbonate → 3-(5-Amino-3-tert-butyl-pyrazol-1-yl)-5-chloro-phenol

https://huagongshe.com/reaction/711180

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
Edukttrans-N,N'-dimethyl-1,2-cyclohexanediamineHCID 2733821—
Edukt3-Bromo-5-chlorophenolHCID 22630180—
EduktHCID 178441179HCID 178441179—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
Produkt3-(5-Amino-3-tert-butyl-pyrazol-1-yl)-5-chloro-phenolHCID 11772975462%

Reaktionsbedingungen

Temperatur110 °C

Reaktionsschritte

A microwave vial containing 3-tert butyl-1h-pyrazol-5-amine (559 mg, 4.02 mmol), Intermediate 62a (1.00 g, 4.82 mmol), copper(I) iodide (38 mg, 0.20 mmol) and potassium carbonate (1.16 g, 8.44 mmol) was repeatedly purged with argon. Trans-N,N′-dimethylcyclohexane-1,2-diamine (126 μL, 0.80 mmol) was added and the mixture was re-purged with argon. Degassed toluene (4 mL) was added and the resulting suspension was stirred and heated at 110° C. for 24 h. The cooled suspension was passed through Celite pad and diluted with water and extracted with EtOAc. The combined organics were dried and concentrated in vacuo. The residue was purified by FCC, using 0-50% EtOAc in cyclohexane, to give the title compound (620 mg, 62%). LCMS (Method 3): Rt 3.13 min, m/z 266 [MH+].

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09181242B2
Quelldatensatzuspto-grants-2015_11
ORD IDord-ee0ba75a78b24892b192b3399fccf60f
Quellennotizuspto-grants-2015_11