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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 549514Generated: October 25, 2026

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

https://huagongshe.com/reaction/549514

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 poured into water (15 mL) and ethyl acetate was added to dissolve the resulting oil. The suspension was then 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 as a light brown oil (0.3 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07943651B2
Source datasetuspto-grants-2011_05
ORD IDord-92d902b491c44d9589d6858c8c2895c6
Source noteuspto-grants-2011_05