Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 407163Generated: October 31, 2026

3-(Trifluoromethyl)benzenesulfonyl chloride → HCID 46234072, compound

https://huagongshe.com/reaction/407163

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Trifluoromethyl)benzenesulfonyl chlorideHCID 2733250—
ReactantHCID 46235778HCID 46235778—
SolventPyridineHCID 1049—
ProductHCID 46234072HCID 46234072—

Reaction Steps

To a stirred solution of ethyl 6-(3-aminophenyl)-1H-indazole-3-carboxylate (10 mg) in pyridine (1 Ml), was added 3-trifluoromethylbenzenesulfonyl chloride (6.3 μl) at room temperature. After 3 h, pyridine was removed by evaporation. Ethyl acetate and water were added and the aqueous layer was extracted with ethyl acetate three times. The combined organic layer was dried over magnesium sulfate and concentrated under reduced pressure. The residue was triturated in ethyl acetate/hexane to give ethyl 6-(3-(3-(trifluoromethyl)phenylsulfonamido)phenyl)-1H-indazole-3-carboxylate (8.6 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08754209B2
Source datasetuspto-grants-2014_06
ORD IDord-438d64a14e1744adb0f0592139139c9a
Source noteuspto-grants-2014_06