HuagongsheHuagongshe Chemistry Print Report · For research reference only
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
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(4-Cyano-2-iodo-5-(trifluoromethyl)phenyl)methanesulfonamide | HCID 21091191 | — |
| Reactant | 1-Ethylsulfanyl-2-methyl-but-3-yn-2-ol | HCID 58979596 | — |
| Product | 2-(2-ethylsulfanyl-1-hydroxy-1-methyl-ethyl)-1-methanesulfonyl-6-trifluoromethyl-1H-indole-5-carbonitrile | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09434688B2 |
| Source dataset | uspto-grants-2016_09 |
| ORD ID | ord-7b84be8c95d24abf92f11203312e1397 |
| Source note | uspto-grants-2016_09 |