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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1945157Generated: November 1, 2026

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

https://huagongshe.com/reaction/1945157

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-[4-Chloro-2-iodo-5-(trifluoromethyl)phenyl]methanesulfonamideHCID 66864554—
Reactant3-(2,2,2-Trifluoro-ethylsulfanylmethyl)-pent-1yn-3-olHCID 86080094—
Product2-(5-chloro-1-methanesulfonyl-6-trifluoromethyl-1H-indol-2-yl)-1-(2,2,2-trifluoro-ethylsulfanyl)-butan-2-olHCID 11663059—

Reaction Steps

This compound was prepared using the standard Sonagashira procedure as described in General Procedures Example C, reacting from N-(4-chloro-2-iodo-5-trifluoromethyl-phenyl)-methanesulfonamide (0.60 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 numberUS08394971B2
Source datasetuspto-grants-2013_03
ORD IDord-a5ceab70f5e94b96a0c69a9d7bc33e6b
Source noteuspto-grants-2013_03