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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1943902Generated: November 1, 2026

Imidazole → HCID 67089020, compound

https://huagongshe.com/reaction/1943902

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
ReactantL-ProlineHCID 145742—
ReactantHCID 178526491HCID 178526491—
SolventDimethyl SulfoxideHCID 679—
SolventIsopropanolHCID 3776—
SolventDichloromethaneHCID 6344—
ProductHCID 67089020HCID 6708902046%

Reaction Conditions

Temperature110 °C

Reaction Steps

Imidazole (280 mg, 4.1 mmol), potassium carbonate (1.40 g, 10 mmol), L-proline (95 mg, 0.82 mmol), and cuprous iodide (78 mg, 0.41 mmol) were added to 3-bromo-5-nitro-pyrazolopyridine (500 mg, 2.1 mmol) in DMSO (5 mL). The resulting mixture was heated in a sealed vial at 110° C. overnight. The reaction mixture was diluted with water and 10% isopropyl alcohol (“IPA”)/DCM. The resulting slurry was filtered through celite, and the layers were separated. The aqueous layer was extracted with another portion of 10% IPA/DCM. The combined organic layers were washed twice with brine, dried over magnesium sulfate, filtered, and evaporated to yield 3-(1H-imidazol-1-yl)-5-nitro-1H-pyrazolo[3,4-b]pyridine (220 mg, 46% yield) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394795B2
Source datasetuspto-grants-2013_03
ORD IDord-cfa48b1f17e845dfb427b801578a75a5
Source noteuspto-grants-2013_03