HuagongsheHuagongshe Chemistry Print Report · For research reference only
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
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-[2-Iodo-4-nitro-5-(trifluoromethyl)phenyl]methanesulfonamide | HCID 58979620 | — |
| Reactant | 3-(2,2,2-Trifluoro-ethylsulfanylmethyl)-pent-1yn-3-ol | HCID 86080094 | — |
| Product | 2-(1-methanesulfonyl-5-nitro-6-trifluoromethyl-1H-indol-2-yl)-1-(2,2,2-trifluoro-ethylsulfanyl)-butan-2-ol | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09434688B2 |
| Source dataset | uspto-grants-2016_09 |
| ORD ID | ord-999dc03a4e684769b61ac26b501dc170 |
| Source note | uspto-grants-2016_09 |