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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 965358Generated: October 30, 2026

Water → 3-[2-(2-Carbamoylhydrazonocyclohexyl)-3-oxo-2,3-dihydropyridazin-6-yl]-2-phenylpyrazolo[1,5-a]pyridine

https://huagongshe.com/reaction/965358

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSemicarbazide hydrochlorideHCID 11236—
ReactantPotassium CarbonateHCID 11430—
Reactant3-[2-(2-Oxocyclohexyl)-3-oxo-2,3-dihydropyridazin-6-yl]-2-phenylpyrazolo[1,5-a]pyridineHCID 11069041—
SolventEthanolHCID 702—
Product3-[2-(2-Carbamoylhydrazonocyclohexyl)-3-oxo-2,3-dihydropyridazin-6-yl]-2-phenylpyrazolo[1,5-a]pyridineHCID 5732149147.4%

Reaction Steps

A mixture of 3-[2-(2-oxocyclohexyl)-3-oxo-2,3-dihydropyridazin-6-yl]-2-phenylpyrazolo[1,5-a]pyridine (231 mg), semicarbazide hydrochloride (101 mg), potassium carbonate (125 mg), water (2 ml), and ethanol (10 ml) was heated under reflux for 4 hours. Ethanol was evaporated in vacuo and the residue was partitioned between dichloromethane (30 ml) and saturated aqueous sodium bicarbonate (30 ml). After an additional extraction with dichloromethane, the combined extracts were washed with brine (20 ml), dried over anhydrous sodium sulfate, and evaporated in vacuo to give colorless crystals of 3-[2-(2-carbamoylhydrazonocyclohexyl)-3-oxo-2,3-dihydropyridazin-6-yl]-2-phenylpyrazolo[1,5-a]pyridine (125.8 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05773530
Source datasetuspto-grants-1998_06
ORD IDord-5af9102793ba4181bb9dcaad7a1505ad
Source noteuspto-grants-1998_06