HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(4-fluoro-2-iodo-5-trifluoromethyl-phenyl)-methanesulfonamide → 2-(5-fluoro-1-methanesulfonyl-6-trifluoromethyl-1H-indol-2-yl)-1-(2,2,2-trifluoro-ethylsulfanyl)-butan-2-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(4-fluoro-2-iodo-5-trifluoromethyl-phenyl)-methanesulfonamide | HCID 58979618 | — |
| Reactant | 3-(2,2,2-Trifluoro-ethylsulfanylmethyl)-pent-1yn-3-ol | HCID 86080094 | — |
| Product | 2-(5-fluoro-1-methanesulfonyl-6-trifluoromethyl-1H-indol-2-yl)-1-(2,2,2-trifluoro-ethylsulfanyl)-butan-2-ol | HCID 11532842 | — |
Reaction Steps
This compound was prepared using the general Sonagashira procedure as describe in General Procedures Example C, reacting N-(4-fluoro-2-iodo-5-trifluoromethyl-phenyl)-methanesulfonamide (0.57 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 brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07705147B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-57bb3454ee7642b5bf205e36210f2089 |
| Source note | uspto-grants-2010_04 |