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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 433888Generated: October 26, 2026

Ammonium Chloride → Pyridazine-3-carboximidamide hydrochloride

https://huagongshe.com/reaction/433888

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium MethoxideHCID 10942334—
ReactantPyridazine-3-carbonitrileHCID 13642940—
SolventMethanolHCID 887—
ProductPyridazine-3-carboximidamide hydrochlorideHCID 1875608055.9%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06670362B2
Source datasetuspto-grants-2003_12
ORD IDord-4d38f28890454466b2bef50e1624ad75
Source noteuspto-grants-2003_12