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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1906733Generated: October 31, 2026

Pyridine → HCID 178485028, compound

https://huagongshe.com/reaction/1906733

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantIci 109,081HCID 161928—
ReactantHCID 12295279HCID 12295279—
ProductHCID 178485028HCID 178485028—

Reaction Steps

To a solution of N-cyano-N1 -methyl-O-phenylisourea (0.175 g) in anhydrous pyridine (3 ml) was added 6-(4-aminophenyl)-5-methyl-4,5-dihydro-3(2H)-pyridazinone (0.2 g). The mixture was stirred at room temperature for 3 hours, stirred under reflux for 4 hours and allowed to cool overnight. This mixture was evaporated under reduced pressure to give a solid which was triturated with diethyl ether to remove phenol. Thin layer chromatography indicated the presence of unreacted starting-material and the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04654342
Source datasetuspto-grants-1987_03
ORD IDord-4890a8b411b3493abd3b50f131b6a305
Source noteuspto-grants-1987_03