HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 915014Generated: October 30, 2026
p-Toluenesulfonic acid → HCID 178456629, compound
https://huagongshe.com/reaction/915014
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Aminomalononitrile | HCID 151258 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 86600906 | HCID 86600906 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178456629 | HCID 178456629 | 26.4% |
Reaction Steps
A mixture of (1-isopropyl-6-oxo-1,6-dihydro-3-pyridazinyl) (oxo)acetaldehyde oxime (11.16 g), aminomalononitrile (13.6 g) and p-toluenesulfonic acid (10.2 g) in 2-propanol (200 ml) was stirred at 50° C. for 3 hours. Water, aq. NaHCO3 and EtOAc were added to the reaction mixture to give a pale yellow precipitate. The precipitate was collected by filtration to obtain 3-amino-6-(1-isopropyl-6-oxo-1,6-dihydro-3-pyridazinyl)-2-pyrazinecarbonitrile 4-oxide (3.84 g) as white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07265120B2 |
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| Source dataset | uspto-grants-2007_09 |
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| ORD ID | ord-ce5bbd6703154f7a809c9d25a9e25b85 |
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| Source note | uspto-grants-2007_09 |
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