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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1047623Generated: November 1, 2026

Bromine → methyl 3-bromo-1-(4-methylphenyl)-1H-indazole-6-carboxylate

https://huagongshe.com/reaction/1047623

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantMethyl 1-(4-methylphenyl)-1H-indazole-6-carboxylateHCID 66661292—
SolventAcetonitrileHCID 6342—
Productmethyl 3-bromo-1-(4-methylphenyl)-1H-indazole-6-carboxylateHCID 6666154874.2%

Reaction Steps

Methyl 1-(4-methylphenyl)-1H-indazole-6-carboxylate (2.7075 g, 10.17 mmol) was dissolved in acetonitrile (102 ml) at 25° C. under Ar. Bromine (1.886 ml, 36.60 mmol) was added. The reaction mixture was allowed to stir for 60 h. The reaction was stopped, quenched by addition of saturated aqueous sodium bicarbonate (40 mL), and the mixture extracted with ethyl acetate (3×35 mL). The combined organic phases were washed with saturated aqueous sodium chloride (1×25 mL), dried (sodium sulfate), filtered, and the solvent evaporated under reduced pressure. The crude product was purified by flash chromatography (RediSep SiO2, 330 g column) on a CombiFlash Rf purification system eluting with ethyl acetate-hexanes (0-5%). The title compound (2.8006 g, 7.55 mmol, 74.2% yield) was recovered as a white solid. LC-MS [M+1]=346.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569512B2
Source datasetuspto-grants-2013_10
ORD IDord-ea5d45fc7af84c999b37ef74aa40b058
Source noteuspto-grants-2013_10