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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372788Generated: October 25, 2026

Potassium Carbonate → methyl 1-((4-methoxyphenyl)methyl)-1H-indazole-3-carboxylate

https://huagongshe.com/reaction/1372788

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Methyloxybenzyl chlorideHCID 69993—
Reactantmethyl 1H-indazole-3-carboxylateHCID 657476—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Productmethyl 1-((4-methoxyphenyl)methyl)-1H-indazole-3-carboxylateHCID 1785901425%

Reaction Conditions

Temperature80 °C

Reaction Steps

Methyl 3-indazolylcarboxylate (2.0 g, 11.4 mmol) was dissolved in DMF (20 ml). To the resulting solution were added 4-methoxybenzyl chloride (1.7 ml, 12.5 mmol) and potassium carbonate (2.35 g, 17.0 mmol). The resulting mixture was stirred at 80° C. for 15 hours. After cooling, the reaction mixture was poured in water (50 ml), followed by extraction with ethyl acetate (200 ml). The extract was washed with saturated brine (2×100 ml), dried over anhydrous magnesium sulfate, and distilled under reduced pressure to remove the solvent. The residue was purified by chromatography on a silica gel column, whereby from hexane-ethyl acetate (4:1) eluate fractions, methyl 1-(4-methoxybenzyl)-3-indazolylcarboxylate (polar fractions, 838 mg, 25%) was obtained as a pale yellow oil and 2(4-methoxybenzyl) isomer (non-polar fractions, 500 mg, 15%) was obtained as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157487B2
Source datasetuspto-grants-2007_01
ORD IDord-c7002c1244cd462b8493fd8eb5681b9c
Source noteuspto-grants-2007_01