HuagongsheHuagongshe Chemistry Print Report · For research reference only
(4-Fluorophenyl)hydrazine → 5-Amino4-(3-bromobenzoyl)-1-(4-fluorophenyl)pyrazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (4-Fluorophenyl)hydrazine | HCID 69982 | — |
| Reactant | 2-(3-Bromobenzoyl)-3-phenylaminoacrylonitrile | HCID 69686607 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 5-Amino4-(3-bromobenzoyl)-1-(4-fluorophenyl)pyrazole | HCID 11451237 | 87.7% |
Reaction Steps
A mixture of 4-fluorophenylhydrazine (4.25 g, 33.7 mmol) and 2-(3-bromobenzoyl)-3-phenylaminoacrylonitrile (10.0 g, 30.7 mmol) in ethanol (100 ml) was heated at reflux under a nitrogen atmosphere. After 4 h, the reaction mixture was cooled to room temperature, diluted with hexane to give 5-amino-4-(3-bromobenzoyl)-1-(4-fluorophenyl)pyrazole (9.7 g) as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06376527B1 |
| Source dataset | uspto-grants-2002_04 |
| ORD ID | ord-10c493b9e8b14faea8efb92fc990d6a5 |
| Source note | uspto-grants-2002_04 |