HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aniline → 5-Imino-1-phenyl-4-(phenylhydrazinylidene)-3-pyrazolamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | Phenylhydrazine | HCID 7516 | — |
| Reactant | Malononitrile | HCID 8010 | — |
| Reactant | Carbonyl cyanide phenylhydrazone | HCID 67541 | — |
| Product | 5-Imino-1-phenyl-4-(phenylhydrazinylidene)-3-pyrazolamine | HCID 318030 | — |
Reaction Steps
1-phenyl-4-phenylazo-1H-pyrazole-3,5-diamine was prepared using 200 mg (1.2 mmol) of 2-(phenylhydrazono)malononitrile, which was derived from aniline (10 mL, 107 mmol) and malononitrile (161 mmol), and phenylhydrazine (767 mg, 7.1 mmol). Solids had not formed after heating the reaction at 75° C. for 3 hrs, however, analysis of the reaction solution by TLC indicated that no starting material remained. The solution was allowed to cool to ambient temperature and the solvent was evaporated. The residue was dissolved in ethyl acetate and then precipitated by the addition of hexanes. The resulting solid was isolated by filtration and dried to yield 77 mg (23%) of the compound as an orange coloured solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08445694B2 |
| Source dataset | uspto-grants-2013_05 |
| ORD ID | ord-051865f2259045fd856c0bd9d870001d |
| Source note | uspto-grants-2013_05 |