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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 512830Generated: October 26, 2026

Water → 1-(6-(1-methyl-1H-pyrazol-4-yl)pyridazin-3-yl)piperidin-4-one

https://huagongshe.com/reaction/512830

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant8-(6-(1-methyl-1H-pyrazol-4-yl)pyridazin-3-yl)-1,4-dioxa-8-azaspiro[4.5]decaneHCID 89614330—
SolventPropan-2-one--water (1/1)HCID 18366337—
Product1-(6-(1-methyl-1H-pyrazol-4-yl)pyridazin-3-yl)piperidin-4-oneHCID 89613995—

Reaction Conditions

Temperature65 °C

Reaction Steps

To a solution of 8-(6-(1-methyl-1H-pyrazol-4-yl)pyridazin-3-yl)-1,4-dioxa-8-azaspiro[4.5]decane, prepared as in STEP 2 above (1.8 g, 6 mmol) in acetone/H2O (30 mL/30 mL) was added p-TSA.H2O (1.37 g, 7.2 mmol). The resulting mixture was stirred at 65° C. for 6 h and then concentrated to remove most of organic solvent. The residue was poured into CH2Cl2/H2O/Na2CO3(aq) (50 mL/25 mL/25 mL). The aqueous layer was extracted with CH2Cl2 (50 mL). The combined organic layer was dried (Na2SO4), and filtered. The solvent was removed by roto-evaporator to yield 1-(6-(1-methyl-1H-pyrazol-4-yl)pyridazin-3-yl)piperidin-4-one as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09102669B2
Source datasetuspto-grants-2015_08
ORD IDord-10090d5e173e47dd946086cf3c303c49
Source noteuspto-grants-2015_08