HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 18616782, compound → HCID 18616705, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 18616782 | HCID 18616782 | — |
| Catalyst | HCID 178506449 | HCID 178506449 | — |
| Product | HCID 18616705 | HCID 18616705 | 71.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06541481B2 |
| Source dataset | uspto-grants-2003_04 |
| ORD ID | ord-a26a5e9dfa4f47e7a9624c5a738aed2e |
| Source note | uspto-grants-2003_04 |