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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2196402Generated: October 29, 2026

Potassium Carbonate → 5-(1-methyl-1H-pyrazol-5-yl)pyrimidine-2-carboxylic acid

https://huagongshe.com/reaction/2196402

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-methyl-5-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazoleHCID 4912908—
Reactant5-Bromopyrimidine-2-carboxylic acidHCID 16462970—
CatalystHCID 178418397HCID 178418397—
Solvent1,4-Dioxane--water (1/1)HCID 21886435—
Product5-(1-methyl-1H-pyrazol-5-yl)pyrimidine-2-carboxylic acidHCID 5935499074.7%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 1-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (1.35 g, 6.5 mmol) in dioxane/H2O (5:1, 59 mL) was added K2CO3 (2.8 g, 20.3 mmol), tetrakistriphenylphosphine Pd(0) (340 mg, 0.3 mmol), and 5-bromo-2-pyrimidinecarboxylic acid (1.2 g, 5.9 mmol). The reaction mixture was heated to 80° C. in a sealed tube for 12 h. The reaction solution was poured onto H2O (100 mL) and extracted with DCM. The organics were dried (Na2SO4), concentrated under vacuum to give the title compound (0.9 g, 36%) as a tan solid: LC-MS (ES) m/z=437 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338434B2
Source datasetuspto-grants-2012_12
ORD IDord-d3356a7b41aa466599c252170fe17002
Source noteuspto-grants-2012_12