HuagongsheHuagongshe Chemistry Print Report · For research reference only
(4-Fluorophenyl)hydrazine → 5-Amino-4-(3-iodobenzoyl)-1-(4-fluorophenyl)pyrazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (4-Fluorophenyl)hydrazine | HCID 69982 | — |
| Reactant | 2-(3-Iodobenzoyl)-3-phenylaminoacrylonitrile | HCID 67024274 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 5-Amino-4-(3-iodobenzoyl)-1-(4-fluorophenyl)pyrazole | HCID 9866075 | 87.4% |
Reaction Steps
A mixture of 4-fluorophenylhydrazine (26.6 g, 211 mmol) and 2-(3-iodobenzoyl)-3-phenylaminoacrylonitrile (79 g, 211 mmol) in ethanol (400 ml) was heated at reflux under a nitrogen atmosphere. After 30 minutes, the reaction mixture was cooled to room temperature, diluted with hexane to give 5-amino-4-(3-iodobenzoyl)-1-(4-fluorophenyl)pyrazole (75.1 g) as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06444696B1 |
| Source dataset | uspto-grants-2002_09 |
| ORD ID | ord-7a4462b13858470db849ff31590f8a87 |
| Source note | uspto-grants-2002_09 |