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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1272732Erstellt: 26. Oktober 2026

5-Nitro-3-phenyl-1H-indazole → 3-Phenyl-1H-indazol-5-amine

https://huagongshe.com/reaction/1272732

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt5-Nitro-3-phenyl-1H-indazoleHCID 617444—
KatalysatorPalladiumHCID 23938—
LösungsmittelEthyl AcetateHCID 8857—
Produkt3-Phenyl-1H-indazol-5-amineHCID 2248010488%

Reaktionsschritte

A suspension of 5-nitro-3-phenyl-1H-indazole (0.239 g, 1.0 mmol) and palladium (10 wt % on activated carbon, 30 mg) in ethyl acetate (10 mL) was stirred under hydrogen at ambient temperature for 18 hours. It was filtered with celite and washed with ethyl acetate. The filtrate was concentrated and the residue was then purified by chromatography (SiO2, 30–50% ethyl acetate/hexane) to provide the title compound (0.184 g, 88% yield): mp 104° C.; 1H NMR (CDCl3) δ 10.40 (br s, 1H), 7.94 (d, 2H), 7.51 (m, 2H), 7.20–7.42 (m, 3H), 6.90 (m, 1H), 3.6 (br, 2H); EI-MS (m/z) 209 [M]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07208513B2
Quelldatensatzuspto-grants-2007_04
ORD IDord-f229d86b9cb7419fb9d0b87e204e3d62
Quellennotizuspto-grants-2007_04