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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1264035Generated: October 30, 2026

HCID 18616782, compound → HCID 18616705, compound

https://huagongshe.com/reaction/1264035

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 18616782HCID 18616782—
CatalystHCID 178506449HCID 178506449—
ProductHCID 18616705HCID 1861670571.5%

Reaction Steps

To a solution of 2-chloro-5-nitro-benzophenone (1.0 g) in THF (tetrahydrofuran) (15 ml) was added anhydrous hydrazine (120 mg). The resulting reaction mixture was kept stirring at room temperature for 2-4 hours. The solvent was removed in vacuo and the residue dissolved in EtOAc, washed with water and brine, dried over Na2SO4. Removal of the solvent afforded (0.8 g, 88%) product 6-Nitro-3-phenyl-1H-indazole (5). 6-Nitro-3-phenyl-1H-indazole was hydrogenated over H2/Pd and gave 0.5 g of 3-phenyl-1H-indazol-6-ylamine (71.5%). M/z: 210.0. 1H NMR (CD3OD): 7.86 (d, 2H, J=7.9 Hz), 7.47 (t, J=8.1 Hz), 7.35 (t, 3H, J=8.7 Hz), 7.01 (d, 1H, J=8.7 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06541481B2
Source datasetuspto-grants-2003_04
ORD IDord-a26a5e9dfa4f47e7a9624c5a738aed2e
Source noteuspto-grants-2003_04