HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Ethylsulfanyl-2-methyl-but-3-yn-2-ol → 1-Ethylsulfanyl-2-(5-fluoro-1-methanesulfonyl-6-trifluoromethyl-1H-indol-2-yl)-propan-2-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Ethylsulfanyl-2-methyl-but-3-yn-2-ol | HCID 58979596 | — |
| Reactant | N-(4-fluoro-2-iodo-5-trifluoromethyl-phenyl)-methanesulfonamide | HCID 58979618 | — |
| Product | 1-Ethylsulfanyl-2-(5-fluoro-1-methanesulfonyl-6-trifluoromethyl-1H-indol-2-yl)-propan-2-ol | HCID 11611014 | — |
Reaction Steps
This compound was prepared using the general Sonagashira procedure as described in the General Procedures Example C. The starting material was N-(4-fluoro-2-iodo-5-trifluoromethyl-phenyl)-methanesulfonamide (0.77 g, 2.0 mmol) and 1-ethylsulfanyl-2-methyl-but-3-yn-2-ol (0.29 g, 2.0 mmol), reacted to yield the title compound as a golden oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09434688B2 |
| Source dataset | uspto-grants-2016_09 |
| ORD ID | ord-90d17e8e63f24955b2916d8f9f738d7b |
| Source note | uspto-grants-2016_09 |