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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1255858Generated: November 3, 2026

Sodium Bicarbonate → 3-Bromo-6-pyridin-3-ylpyrazolo[1,5-a]pyrimidine

https://huagongshe.com/reaction/1255858

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant3-Pyridinylboronic acidHCID 2734378—
Reactant3,6-Dibromopyrazolo(1,5-a)pyrimidineHCID 12203209—
SolventDimethylformamideHCID 6228—
Product3-Bromo-6-pyridin-3-ylpyrazolo[1,5-a]pyrimidineHCID 68777060—

Reaction Conditions

Temperature85 °C

Reaction Steps

A solution of 3-pyridyl boronic acid (1.33 g, 10.8 mmol) and 3,6-dibromopyrazolo[1,5-a]pyrimidine (3.0 g, 10.8 mmol) in DMF (300 mL) and 1M aqueous sodium bicarbonate (22 mL, 22 mmol) was degassed with nitrogen and treated with palladium tetrakistriphenylphosphine (0.63 g, 0.54 mmol) and heated to 85° C. for 16 hours. The reaction was cooled to room temperature and partitioned between water/methylene chloride. The organics were washed with water and brine, dried over sodium sulfate, filtered and evaporated in vacuo. Purification by flash chromatography (1-5% methanol/methylene chloride) gave 3-bromo-6-pyridin-3-ylpyrazolo[1,5-a]pyrimidine. LC-MS EIMS: m/z 275.0 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461162B2
Source datasetuspto-grants-2013_06
ORD IDord-ffdaa4444e3548e5a0996494f2ff854a
Source noteuspto-grants-2013_06