HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 433888Generated: October 26, 2026
Ammonium Chloride → Pyridazine-3-carboximidamide hydrochloride
https://huagongshe.com/reaction/433888
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | Pyridazine-3-carbonitrile | HCID 13642940 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Pyridazine-3-carboximidamide hydrochloride | HCID 18756080 | 55.9% |
Reaction Steps
Sodium methoxide (25% w/v in methanol, 0.3 ml, 1.3 mmol) was added in one portion to a stirred solution of 3-cyanopyridazine (2.4 g g, 22.9 mmol) (Ref. Heterocycles, 1986, 24(3), 793) in methanol (10 ml). The resulting mixture was stirred at room temperature for 16 hours. Ammonium chloride (2.45 g, 45.8 mmol) was added to the reaction mixture, which was then stirred for 30 minutes before being ultrasonicated for a further 15 minutes. A fine, yellow precipitate was observed after this time. The solvent was evaporated under vacuum and the residue was suspended in ethanol (150 ml) and heated to reflux for 5 minutes. The hot mixture was filtered (gravity) to remove unreacted ammonium chloride and sodium chloride and was then cooled to room temperature. A pale yellow, crystalline solid formed upon cooling and this was isolated by suction filtration to give the title compound (2.03 g), m.p. 234°-241° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06670362B2 |
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| Source dataset | uspto-grants-2003_12 |
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| ORD ID | ord-4d38f28890454466b2bef50e1624ad75 |
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| Source note | uspto-grants-2003_12 |
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