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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 879316Generated: October 31, 2026

Sodium Carbonate → 5-(1-methyl-1H-indazol-5-yl)pyridin-2(1H)-one

https://huagongshe.com/reaction/879316

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant1-Methyl-1H-indazole-5-boronic acidHCID 22558910—
ReactantHCID 178515818HCID 178515818—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product5-(1-methyl-1H-indazol-5-yl)pyridin-2(1H)-oneHCID 86699835—

Reaction Conditions

Temperature80 °C

Reaction Steps

The suspension of 5-bromo-2-hydroxypyridine (80 mg, 0.46 mmol), 1-methyl-1H-indazol-5-ylboronic acid (121 mg, 0.69 mmol) and 2N sodium carbonate solution (1.0 mL, 2 mmol) in DMF (2.1 mL) was degassed with N2 for 5 minutes. To the mixture was added tetrakis(triphenylphosphine)palladium(0) (53 mg, 0.04 mmol), and the resulting mixture was heated at 80° C. overnight. The mixture was then diluted with CH2Cl2, extracted with H2O, brine, dried over Na2SO4, filtered and concentrated and purified by reverse phase HPLC (Gemini, 5 to 100% ACN/H2O+0.1% TFA) to give the product. LCMS-ESI+ (m/z): [M+H]+ calcd for C13H12N3O: 226.25; Found: 226.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987250B2
Source datasetuspto-grants-2015_03
ORD IDord-b6eca57d68f6421ea53133377c448936
Source noteuspto-grants-2015_03