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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 512829Generated: October 30, 2026

Potassium Carbonate → 8-(6-(1-methyl-1H-pyrazol-4-yl)pyridazin-3-yl)-1,4-dioxa-8-azaspiro[4.5]decane

https://huagongshe.com/reaction/512829

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazoleHCID 2773987—
Reactant8-(6-Chloropyridazin-3-yl)-1,4-dioxa-8-azaspiro[4.5]decaneHCID 3226717—
CatalystHCID 178418397HCID 178418397—
Product8-(6-(1-methyl-1H-pyrazol-4-yl)pyridazin-3-yl)-1,4-dioxa-8-azaspiro[4.5]decaneHCID 89614330—

Reaction Conditions

Temperature100 °C

Reaction Steps

In a two-neck flask was placed 8-(6-chloropyridazin-3-yl)-1,4-dioxa-8-azaspiro[4.5]decane, prepared as in STEP 1 above (3.07 g, 12 mmol), 1-methylpyrazole-4-boronic acid pinacol ester (3.24 g, 15.6 mmol), K2CO3 (6.62 g, 48 mmol), and Pd(PPh3)4 (693 mg, 0.6 mmol). The resulting mixture was degassed and refilled with N2 (3 times). 1,4-Dioxane/H2O (15 mL/5 mL) was added and the resulting mixture was heated at 100° C. for 4 h. The resulting mixture was then poured into EtOAc/H2O (100 mL/100 mL). The organic layer was washed with brine (100 mL), dried (Na2SO4), and filtered. The solvent was removed by roto-evaporator and the resulting residue purified by column using EtOAc as the eluent to yield 8-(6-(1-methyl-1H-pyrazol-4-yl)pyridazin-3-yl)-1,4-dioxa-8-azaspiro[4.5]decane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09102669B2
Source datasetuspto-grants-2015_08
ORD IDord-1fd20e3362bb4862a162d577ee417953
Source noteuspto-grants-2015_08