Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 58069Generated: October 25, 2026

Sodium Carbonate → 4-phenyl-6-(trifluoromethyl)-1H-indazole

https://huagongshe.com/reaction/58069

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantPhenylboronic AcidHCID 66827—
Reactant4-Bromo-6-(trifluoromethyl)-1H-indazoleHCID 24729232—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
Solvent1,4-DioxaneHCID 31275—
ProductTrifluoroacetic acidHCID 6422—
Product4-phenyl-6-(trifluoromethyl)-1H-indazoleHCID 7173520570.8%

Reaction Conditions

Temperature120 °C

Reaction Steps

A vessel was charged with 4-bromo-6-(trifluoromethyl)-1H-indazole (0.1 g, 0.377 mmol), phenylboronic acid (0.069 g, 0.566 mmol), PdCl2(dppf) (0.014 g, 0.019 mmol), and dioxane (3 mL). To the resulting slurry was added 2N aqueous sodium carbonate (0.377 mL, 0.755 mmol). The mixture was purged with nitrogen, heated in a microwave reactor at 120° C. for 30 minutes, and then filtered through a pad of Celite, which was rinsed with methanol. The solvent was removed in vacuo, and the resulting residue was taken up in DMSO and methanol (1:1) and was purified via acidic preparative HPLC (Waters SunFire C18, 5 μm, 30 mm ID×75 mm column), eluting with a gradient of 55-80% ACN (containing 0.035% TFA) in H2O (containing 0.05% TFA). The collected fractions were dried in vacuo to give a TFA salt of the title compound as a tan solid (35 mg, 35%). 1H NMR (400 MHz, CDCl3) δ ppm 7.43-7.62 (m, 4H), 7.71 (d, J=7.07 Hz, 2H), 7.83 (s, 1H), 8.23-8.38 (m, 1H), 8.47 (br s, 1H); ESI-MS m/z [M+H]+ calc'd for C14H9F3N2, 263.1. found 263.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434743B2
Source datasetuspto-grants-2016_09
ORD IDord-707602f09c814b598495f3146da421bc
Source noteuspto-grants-2016_09