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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1522506Generated: November 4, 2026

1,4-Dioxane → HCID 68079252, compound

https://huagongshe.com/reaction/1522506

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DioxaneHCID 31275—
ReactantSodium BicarbonateHCID 516892—
Reactant3-Pyridinylboronic acidHCID 2734378—
ReactantHCID 86677625HCID 86677625—
CatalystHCID 178418807HCID 178418807—
SolventEthyl AcetateHCID 8857—
ProductHCID 68079252HCID 68079252—

Reaction Steps

Ethyl 1-(1,1-dimethylethyl)-3-methyl-6-{[(trifluoromethyl)sulfonyl]oxy}-1H-pyrazolo[3,4-b]pyridine-4-carboxylate (100 mg, 0.244 mmol), 3-pyridinylboronic acid (39.0 mg, 0.318 mmol), aq. saturated NaHCO3 (1 mL) and 1,4-dioxane (3 mL) were degassed with nitrogen (10 min) followed by addition of PdCl2(dppf)-CH2Cl2 adduct (9.97 mg, 0.012 mmol). The sealed mixture was irradiated (microwave) at 120° C. for 40 min. The reaction mixture was diluted with EtOAc and filtered. The filtrate was concentrated in vacuo and the crude residue was purified by silica gel chromatography (0 to 100% EtOAc/hexanes). The final product was collected as a solid, 72 mg (87%). LCMS E-S (M+H)=339.3. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.46-1.57 (m, 3 H), 1.90 (s, 9 H), 2.72 (s, 3 H), 4.45-4.64 (m, 2 H), 7.47 (dd, J=8.08, 4.80 Hz, 1 H), 8.03 (s, 1 H), 8.46 (dt, J=8.08, 2.02 Hz, 1 H), 8.72 (dd, J=4.80, 1.52 Hz, 1 H), 9.43 (d, J=1.52 Hz, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073924B2
Source datasetuspto-grants-2015_07
ORD IDord-aa7dd9a07b8e4b49a036fa96caa6f3a6
Source noteuspto-grants-2015_07