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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 407153Generated: October 26, 2026

Ethanol → Ethyl 6-bromo-1H-indazole-3-carboxylate

https://huagongshe.com/reaction/407153

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantThionyl ChlorideHCID 24386—
Reactant6-Bromo-1H-indazole-3-carboxylic acidHCID 24728028—
ProductEthyl 6-bromo-1H-indazole-3-carboxylateHCID 51358649—

Reaction Steps

To a stirred solution of 6-bromo-1H-indazole-3-carboxylic acid (5 g, 21 mmol) in ethanol (160 Ml), thionyl chloride (8 Ml, 104 mmol; SOCl2) was added. The mixture was refluxed for 3 h, cooled to room temperature, and concentrated under reduced pressure. Ethyl acetate was added. The organic layer was washed with saturated sodium bicarbonate solution, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified by flash column chromatography (silica gel, DCM:MeOH=9:1) to give ethyl 6-bromo-1H-indazole-3-carboxylate (2.8 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08754209B2
Source datasetuspto-grants-2014_06
ORD IDord-8822949004f946debace9372bfdae753
Source noteuspto-grants-2014_06