HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
2-(Di-tert-butylphosphino)biphenyl → (r)-4-(3-Methylpiperazin-1-yl)-n-(1,2,4-thiadiazol-5-yl)benzenesulfonamide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 2-(Di-tert-butylphosphino)biphenyl | HCID 2734215 | — |
| Edukt | 2-Methylpiperazine, (R)- | HCID 7330434 | — |
| Edukt | 4-bromo-N-(1,2,4-thiadiazol-5-yl)benzenesulfonamide | HCID 53627606 | — |
| Edukt | sodium 2-methylpropan-2-olate | HCID 178418730 | — |
| Katalysator | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | (r)-4-(3-Methylpiperazin-1-yl)-n-(1,2,4-thiadiazol-5-yl)benzenesulfonamide | HCID 59465674 | 19% |
Reaktionsschritte
Synthesized according to general procedure 8. The reaction was set up with 4-bromo-N-(1,2,4-thiadiazol-5-yl)benzenesulfonamide (4.7 mmol), (R)-2-methylpiperazine (4.7 mmol), Pd2(dba)3 (0.12 mmol), 2-(di-t-butylphosphino)biphenyl (0.50 mmol), NaO-tBu (10 mmol), and toluene (12 mL). For the purification, 10% MeOH in CH2Cl2 with the addition of 1% triethylamine was used as a solvent system to obtain the desired amine as a white solid (300 mg, 19% yield). LC/MS (10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA)), m/z: M+1 obs=340.2; tR=1.56 min.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08163720B2 |
| Quelldatensatz | uspto-grants-2012_04 |
| ORD ID | ord-fdeba54becc1465bbb3f678457cdc1a2 |
| Quellennotiz | uspto-grants-2012_04 |