Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 502226Generated: November 4, 2026

Ethanesulfonyl chloride → HCID 46946630, compound

https://huagongshe.com/reaction/502226

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanesulfonyl chlorideHCID 11667—
ReactantHCID 59426292HCID 59426292—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
ProductHCID 46946630HCID 4694663083%

Reaction Steps

To a solution of the compound obtained in step C (31 mg, 0.1 mmol) in dry pyridine (1.0 mL) is added ethanesulfonyl chloride (14 μL, 0.15 mmol). The mixture is stirred at room temperature overnight and diluted with water (5 mL). The organic is extracted with DCM (5 mL) and washed with HCl (2N, 2×3 mL), water (2×4 mL) and brine (3 mL) and chromatographed (silica gel, EtOAc/DCM, 0.5/9.5) to provide the product, ethanesulfonic acid [4-(3-cyano-1-ethyl-6-trifluoromethoxyindol-2-yl)phenyl]amide (33 mg, 83%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772271B2
Source datasetuspto-grants-2010_08
ORD IDord-79fed7e612eb4372b2490b2529483d46
Source noteuspto-grants-2010_08