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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1529372Generated: October 27, 2026

Sodium Carbonate → 5-(6-cyclopropylpyrazin-2-yl)-1H-indazole

https://huagongshe.com/reaction/1529372

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant1H-Indazole-5-boronic acid pinacol esterHCID 17750469—
Reactant2-Bromo-6-cyclopropylpyrazineHCID 45788305—
CatalystHCID 178418397HCID 178418397—
Solvent1,4-DioxaneHCID 31275—
Product5-(6-cyclopropylpyrazin-2-yl)-1H-indazoleHCID 6796008146%

Reaction Conditions

Temperature100 °C

Reaction Steps

A reaction vessel was charged with 2-bromo-6-cyclopropylpyrazine (1.27 g, 6.39 mmol, Combi-Phos Catalysts Inc.) and Pd(PPh3)4 (308 mg, 0.27 mmol). The tube was sealed. A solution of 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazole (1.30 g, 5.33 mmol) in dioxane (18 mL) and 2 M Na2CO3 (aq.) (8.0 mL, 16.0 mmol) were added. The reaction was stirred and heated at 100° C. overnight. After cooling to RT, the organic layer was separated and dried over anhydrous Na2SO4, filtered and concentrated. The crude was purified by silica gel chromatography, eluting with a gradient of 0-50% EtOAc in hexanes, to provide 5-(6-cyclopropylpyrazin-2-yl)-1H-indazole (575 m g, 2.43 mmol, 46% yield) as an off-white solid. MS (ESI, pos. ion) m/z: 237.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09090593B2
Source datasetuspto-grants-2015_07
ORD IDord-2313e9c261c34a139d745733df2e4f6b
Source noteuspto-grants-2015_07