HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
4-Bromobenzenesulfonamide → 2-Phenylbenzene-1-sulfonamide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 4-Bromobenzenesulfonamide | HCID 69696 | — |
| Katalysator | Palladium | HCID 23938 | — |
| Produkt | 2-Phenylbenzene-1-sulfonamide | HCID 12371520 | — |
Reaktionsschritte
In Scheme 1 the compounds of the invention, 1, are prepared in 4 steps. Sulfonylation of valine methyl ester with 4-bromo-benzenesulfonyl chloride was carried out in the presence of Hunig base to give sulfonamide Intermediate 1. This 4-bromo-benzenesulfonamide was furthered coupled with boronate ester using Palladium catalyst under Suzuki coupling condition to provide biphenyl sulfonamide Intermediate 2. Biphenyl sulfonamide Intermediate 2 was then alkylated with various alkylating reagents to provide biphenyl sulfonamide ester (Intermediate 3). Hydrolysis of Intermediate 3 was carried out using bases such as NaOH, or LiOH to form the final product 1.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07390833B2 |
| Quelldatensatz | uspto-grants-2008_06 |
| ORD ID | ord-68ca173bd40c4077ab21cedd0d8e35de |
| Quellennotiz | uspto-grants-2008_06 |