Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1594817Generated: October 31, 2026

HCID 18616782, compound → HCID 18616705, compound

https://huagongshe.com/reaction/1594817

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 9 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 numberUS06284764B1
Source datasetuspto-grants-2001_09
ORD IDord-5f23c91a65f64f44b417ca3ce7c7f22c
Source noteuspto-grants-2001_09