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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1009638Generated: October 31, 2026

Ethanesulfonyl chloride → HCID 46946630, compound

https://huagongshe.com/reaction/1009638

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 numberUS07973069B2
Source datasetuspto-grants-2011_07
ORD IDord-6feecf1b65df4d6ca7cb1ecda7adea18
Source noteuspto-grants-2011_07