Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 902539Generated: October 26, 2026

Potassium Phosphate, Tribasic → 2,3-dimethyl-7-(2,4,6-trimethyl-phenyl)-2H-indazole

https://huagongshe.com/reaction/902539

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant2,4,6-Trimethylbenzeneboronic acidHCID 292184—
Reactant2-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenylHCID 2734217—
Reactant7-Bromo-2,3-dimethyl-2H-indazoleHCID 44119473—
Catalystpalladium(II) acetateHCID 167845—
Product2,3-dimethyl-7-(2,4,6-trimethyl-phenyl)-2H-indazoleHCID 58861008—

Reaction Conditions

Temperature100 °C

Reaction Steps

A flask containing 7-bromo-2,3-dimethyl-2H-indazole (3.23 g, 14.4 mmol), 2,4,6-trimethylphenyl boronic acid (3.51 g, 21.4 mmol), freshly ground potassium phosphate (6.04 g, 28.5 mmol), 2-dicyclohexylphosphino-2′-(N,N-dimethylamino)biphenyl (0.225 g, 0.572 mmol), and palladium(II) acetate (0.032 g, 0.14 mmol) was evacuated and back-filled with nitrogen. Toluene (50 mL) was added, and the yellow-orange mixture was stirred at 100° C. for 22 h then allowed to cool. Ether (200 mL) was added, and the yellow solution was decanted from a dark granular solid. The organic layer was sequentially washed with 200 mL of a 10% aqueous NaOH solution and 200 mL of a saturated aqueous NaCl solution, dried over MgSO4, filtered, and concentrated to a pale yellow solid. Column chromatography (0→33% EtOAc/hexanes) afforded 2,3-dimethyl-7-(2,4,6-trimethyl-phenyl)-2H-indazole as an off-white solid (7: R=R′=Me, Ar=2,4,6-trimethylphenyl; 3.03 g, 79%; m.p. 162-164).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07365211B2
Source datasetuspto-grants-2008_04
ORD IDord-c44bf591ad4445368af7fa648eed8a54
Source noteuspto-grants-2008_04