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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 508193Generated: October 29, 2026

Triethylamine → 3-bromo-1-(2-(trifluoromethyl)phenylsulfonyl)-1H-indazole

https://huagongshe.com/reaction/508193

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Trifluoromethylbenzenesulphonyl chlorideHCID 136616—
ReactantHCID 178419483HCID 178419483—
SolventDichloromethaneHCID 6344—
Product3-bromo-1-(2-(trifluoromethyl)phenylsulfonyl)-1H-indazoleHCID 6815927286.9%

Reaction Steps

To a suspension of 3-bromoindazole (500 mg, 2.54 mmol) in 8 ml CH2Cl2 was added triethyl amine (1.06 ml, 7.61 mmol) at room temperature. To this yellow solution was added 2-(trifluoromethyl)benzenesulfonyl chloride (0.392 ml, 2.54 mmol) and the reaction mixture was stirred for 3 h at room temperature. The reaction mixture was concentrated under reduced pressure and the residue was purified on SiO2 using 5% to 20% ethyl acetate in heptane to give 3-bromo-1-(2-(trifluoromethyl)phenylsulfonyl)-1H-indazole (894 mg)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09095583B2
Source datasetuspto-grants-2015_08
ORD IDord-9bb6984f92b749809f85999c622bd14c
Source noteuspto-grants-2015_08