HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Chlorosuccinimide → 3-Chloromethylthio-7-fluoro-1-methyl-4-quinolone
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Chlorosuccinimide | HCID 31398 | — |
| Edukt | 7-Fluoro-1-methyl-3-methylthio-4-quinolone | HCID 86589151 | — |
| Edukt | HCID 178481179 | HCID 178481179 | — |
| Produkt | 3-Chloromethylthio-7-fluoro-1-methyl-4-quinolone | HCID 10445208 | — |
Reaktionsschritte
In other embodiments, the synthesis of racemic monochloroflosequinan is carried out as a three step procedure, as described in more detail in Example 2. Briefly, in the first step, racemic flosequinan is reduced to desoxyflosequinan (7-fluoro-1-methyl-3-methylthio-4-quinolone). In the second step, desoxyflosequinan is chlorinated using N-chlorosuccinimide, to produce chlorodesoxyflosequinan (3-chloromethylthio-7-fluoro-1-methyl-4-quinolone). In the third step, chlorodesoxyflosequinan is subjected to oxidation to produce 3-chloromethylsulfinyl-7-fluoro-1-methyl-4-quinolone (monochloroflosequinan). Such oxidation may be accomplished using hydrogen peroxide.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07041677B2 |
| Quelldatensatz | uspto-grants-2006_05 |
| ORD ID | ord-111e4bb3897742598ea1fd5eb9eaa3a6 |
| Quellennotiz | uspto-grants-2006_05 |