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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-methyl-5-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole | HCID 4912908 | — |
| Reactant | 5-Bromopyrimidine-2-carboxylic acid | HCID 16462970 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,4-Dioxane--water (1/1) | HCID 21886435 | — |
| Product | 5-(1-methyl-1H-pyrazol-5-yl)pyrimidine-2-carboxylic acid | HCID 59354990 | 74.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08338434B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-d3356a7b41aa466599c252170fe17002 |
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| Source note | uspto-grants-2012_12 |
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