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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 475141Erstellt: 23. Oktober 2026

Ethanol → 3-methoxy-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole-4-carbonitrile

https://huagongshe.com/de/reaction/475141

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
Edukt3,4,7,8-Tetramethyl-1,10-phenanthrolineHCID 74265—
EduktHCID 71272550HCID 71272550—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
Produkt3-methoxy-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole-4-carbonitrileHCID 7127223935,7%

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

A mixture of 3-iodo-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole-4-carbonitrile (50 mg, 0.142 mmol), CuI (13.5 g 0.071 mmol), CsCO3 (2.7 mg, 0.0142 mmol), and 3,4,7,8-tetramethyl-1,10-phenanthroline (0.0142 mg, 3.5 mmol) in EtOH (0.5 mL) under nitrogen in a sealed vial was heated to 90° C. in a microwave oven for 100 min. The reaction mixture was quenched with water and extracted with EtOAc. The extract was dried (MgSO4), filtered, and concentrated in vacuo. The residue was purified by SiO2 chromatography eluting with petroleum ether:EtOAc to afford 3-methoxy-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole-4-carbonitrile as white solid (13 mg, 35.7%). MS (ESI): m/z=258 [M+1]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08637537B2
Quelldatensatzuspto-grants-2014_01
ORD IDord-e03f189af0724914bfbf36403b22ab3f
Quellennotizuspto-grants-2014_01