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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 32936Generated: October 30, 2026

N-[2-Iodo-4-nitro-5-(trifluoromethyl)phenyl]methanesulfonamide → 2-(1-methanesulfonyl-5-nitro-6-trifluoromethyl-1H-indol-2-yl)-1-(2,2,2-trifluoro-ethylsulfanyl)-butan-2-ol

https://huagongshe.com/reaction/32936

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-[2-Iodo-4-nitro-5-(trifluoromethyl)phenyl]methanesulfonamideHCID 58979620—
Reactant3-(2,2,2-Trifluoro-ethylsulfanylmethyl)-pent-1yn-3-olHCID 86080094—
Product2-(1-methanesulfonyl-5-nitro-6-trifluoromethyl-1H-indol-2-yl)-1-(2,2,2-trifluoro-ethylsulfanyl)-butan-2-olHCID 11504175—

Reaction Steps

This compound was prepared using the general Sonagashira procedure as described in General Procedures Example C, reacting N-(2-iodo-4-nitro-5- trifluoromethyl-phenyl) -methanesulfonamide (0.62 g, 1.5 mmol) and 3-(2,2,2-Trifluoro-ethylsulfanylmethyl) -pent-1yn-3-ol (0.32 g, 1.5 mmol) to yield the title compound as a yellow sticky oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07427682B2
Source datasetuspto-grants-2008_09
ORD IDord-193630d568814e61aeee6716b3ec60f1
Source noteuspto-grants-2008_09