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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 58072Generated: October 26, 2026

Sodium Carbonate → 4(2,4-dimethoxypyrimidin-5-yl)-6-(trifluoromethyl)-1H-indazole

https://huagongshe.com/reaction/58072

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant5-Bromo-2,4-dimethoxypyrimidineHCID 255719—
Reactant4-(Tetramethyl-1,3,2-dioxaborolan-2-yl)-6-(trifluoromethyl)-1H-indazoleHCID 89782806—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
Solvent1,4-DioxaneHCID 31275—
ProductTrifluoroacetic acidHCID 6422—
Product4(2,4-dimethoxypyrimidin-5-yl)-6-(trifluoromethyl)-1H-indazoleHCID 8978317745.2%

Reaction Conditions

Temperature130 °C

Reaction Steps

4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-6-(trifluoromethyl)-1H-indazole (35 mg, 0.112 mmol), 5-bromo-2,4-dimethoxypyrimidine (24.56 mg, 0.112 mmol), and PdCl2(dppf) (8.21 mg, 0.011 mmol) were dispersed in dioxane (1.5 mL). To the resulting slurry was added 2N aqueous sodium carbonate (0.112 mL, 0.224 mmol). The mixture was purged with nitrogen, heated in a microwave reactor at 130° C. for 50 minutes, and then filtered through a microfiltration frit. Dioxane was stripped with nitrogen. The resulting residue was taken up in DMSO and methanol (1:1) and was purified via preparative HPLC, eluting with a gradient of ACN (containing 0.035% TFA) in H2O (containing 0.05% TFA). The purified fractions were collected to give a TFA salt of the title compound (8.2 mg, 23%). ESI-MS m/z [M+H]+ calc'd for C14H11F3N4O2, 325.1. found 325.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434743B2
Source datasetuspto-grants-2016_09
ORD IDord-c1a4f9d86256414cb555e8b9c9efc9c1
Source noteuspto-grants-2016_09