HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 254978Generated: October 26, 2026
Aniline → 1-(4-bromophenyl)-4-phenylazo-1H-pyrazole-3,5-diamine
https://huagongshe.com/reaction/254978
Participants
| Role | Name | HCID | Charge |
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| Reactant | Aniline | HCID 6115 | — |
| Reactant | Malononitrile | HCID 8010 | — |
| Reactant | 4-Bromophenylhydrazine hydrochloride | HCID 12157 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Carbonyl cyanide phenylhydrazone | HCID 67541 | — |
| Product | 1-(4-bromophenyl)-4-phenylazo-1H-pyrazole-3,5-diamine | HCID 135443434 | — |
Reaction Steps
1-(4-bromophenyl)-4-phenylazo-1H-pyrazole-3,5-diamine was prepared using 85 mg (0.5 mmol) of 2-(phenylhydrazono)malononitrile, which was derived from aniline (10 mL, 107 mmol) and malononitrile (161 mmol), and 4-bromophenylhydrazine hydrochloride (112 mg, 0.5 mmol) with the addition of 0.5 mL of 5% sodium hydroxide solution. 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 methanol and then precipitated by the addition of water. The resulting solid was isolated by filtration and dried to yield 49 mg (27%) of the compound as a brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07875728B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-7d05be4dceed4a2f9344bec6b52aace1 |
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| Source note | uspto-grants-2011_01 |
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