HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 4-Chloro-5,7-difluoro-3-methyl-2-(2-(methylsulfonyl)phenyl)quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Reactant | 4-Chloro-5,7-difluoro-3-methyl-2-(2-(methylthio)phenyl)quinoline | HCID 59631363 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-Chloro-5,7-difluoro-3-methyl-2-(2-(methylsulfonyl)phenyl)quinoline | HCID 59631037 | — |
Reaction Steps
To a stirring solution of 4-chloro-5,7-difluoro-3-methyl-2-(2-(methylthio)phenyl)-quinoline (0.940 g, 2.80 mmol) in THF (20 mL) and water (6.7 mL) was added oxone (4.3 g, 7.00 mmol). The reaction was stirred at rt for 2 h, then 75 mL water was added and the mixture was stirred for 10 min. The resulting precipitate was isolated by filtration, then dissolved in EtOAc, dried over MgSO4, and concentrated to give 4-chloro-5,7-difluoro-3-methyl-2-(2-(methylsulfonyl)phenyl)-quinoline. Mass Spectrum (ESI) m/e=368.0 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08765940B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-7c9df8cd4eef4eb39ad1efdc96fc568f |
| Source note | uspto-grants-2014_07 |