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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 418786Generated: October 25, 2026

Potassium Carbonate → phenylmethyl 3-(4-amino-6-methyl-1H-indazol-1-yl)benzoate

https://huagongshe.com/reaction/418786

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactanttrans-N,N'-dimethyl-1,2-cyclohexanediamineHCID 2733821—
ReactantBenzyl 3-iodobenzoateHCID 22254461—
ReactantHCID 66648350HCID 66648350—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Productphenylmethyl 3-(4-amino-6-methyl-1H-indazol-1-yl)benzoateHCID 5901001132.3%

Reaction Steps

6-Methyl-1H-indazol-4-amine hydrochloride (0.5 g, 2.7 mmol), phenylmethyl 3-iodobenzoate (0.9 g, 2.6 mmol), copper (I) iodide (14 mg, 0.07 mmol), potassium carbonate (1.2 g, 8.68 mmol) and trans-N,N′-dimethyl-1,2-cyclohexanediamine (20 mg, 0.14 mmol) were heated together in DMF (5 mL) at reflux overnight. The mixture was cooled, poured into a mixture of water and ethyl acetate and filtered through celite. The organic phase was separated, combined with a second ethyl acetate extract, washed successively with water and brine and then dried over anhydrous sodium sulphate and evaporated under reduced pressure. The residue was purified by silica gel column chromatography (75 g) eluting with 1 to 5% gradient of ethyl acetate in dichloromethane to give the title compound (0.3 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093281B2
Source datasetuspto-grants-2012_01
ORD IDord-b40f51b893df41e5b053b71a1ed042cd
Source noteuspto-grants-2012_01