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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183092Generated: November 1, 2026

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

https://huagongshe.com/reaction/2183092

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Nitro-3-phenyl-1H-indazoleHCID 617444—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product3-Phenyl-1H-indazol-5-amineHCID 2248010488%

Reaction Steps

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]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06897231B2
Source datasetuspto-grants-2005_05
ORD IDord-999a1b12f3b34566a403ca0006bb7761
Source noteuspto-grants-2005_05