HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Binap, (A+-)- → N-[4-Chloro-2-(pyridine-3-carbonyl)-phenyl]-4-(cis-2,6-dimethyl-morpholin-4-yl)-benzenesulfonamide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Binap, (A+-)- | HCID 634876 | — |
| Edukt | 2,6-Dimethylmorpholine, cis- | HCID 641500 | — |
| Edukt | Potassium phosphate, tribasic, monohydrate | HCID 22031701 | — |
| Edukt | 4-Bromo-N-[4-chloro-2-(pyridine-3-carbonyl)-phenyl]-benzenesulfonamide | HCID 59788554 | — |
| Katalysator | Palladium | HCID 23938 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | N-[4-Chloro-2-(pyridine-3-carbonyl)-phenyl]-4-(cis-2,6-dimethyl-morpholin-4-yl)-benzenesulfonamide | HCID 59788589 | — |
Reaktionsschritte
The title compound was prepared according to the general procedure for the synthesis of heterocyclyl and heteroaryl substituted phenylsulfonyl derivatives previously described, using 4-Bromo-N-[4-chloro-2-(pyridine-3-carbonyl)-phenyl]-benzenesulfonamide 0.3 g (0.66 mmol), potassium phosphate tribasic monohydrate 0.91 g (3.96 mmol), rac-2,2′-bis (diphenylphosphino)-1,1′-binaphthyl 0.12 g (0.198 mmol), cis-2,6-dimethylmorpholine 0.37 g (3.3 mmol) and Pd (dba)3 60 mg (0.066 mmol) in 3 ml DMF, followed by work up and HPLC purification to yield yellow title compound.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07420055B2 |
| Quelldatensatz | uspto-grants-2008_09 |
| ORD ID | ord-478ee7a9c92f4275afedbd1cc4ff7d60 |
| Quellennotiz | uspto-grants-2008_09 |