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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1616199Generated: November 2, 2026

N-(4-Cyano-2-iodo-5-(trifluoromethyl)phenyl)methanesulfonamide → 2-(2-ethylsulfanyl-1-hydroxy-1-methyl-ethyl)-1-methanesulfonyl-6-trifluoromethyl-1H-indole-5-carbonitrile

https://huagongshe.com/reaction/1616199

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(4-Cyano-2-iodo-5-(trifluoromethyl)phenyl)methanesulfonamideHCID 21091191—
Reactant1-Ethylsulfanyl-2-methyl-but-3-yn-2-olHCID 58979596—
Product2-(2-ethylsulfanyl-1-hydroxy-1-methyl-ethyl)-1-methanesulfonyl-6-trifluoromethyl-1H-indole-5-carbonitrileHCID 66865601—

Reaction Steps

This compound was prepared using the general Sonagashira procedure as describe in General Procedures Example C, reacting N-(4-cyano-2-iodo-5-trifluoromethyl-phenyl)-methanesulfonamide (1.0 g, 2.56 mmol) and 1-ethylsulfanyl-2-methyl-but-3-yn-2-ol (0.37 g, 2.56 mmol) to yield the title compound as a yellow sticky oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765782B2
Source datasetuspto-grants-2014_07
ORD IDord-6f41c09196eb497bb211775af7cf57d2
Source noteuspto-grants-2014_07