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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1696090Erstellt: 26. Oktober 2026

2-(Di-tert-butylphosphino)biphenyl → (r)-4-(3-Methylpiperazin-1-yl)-n-(1,2,4-thiadiazol-5-yl)benzenesulfonamide

https://huagongshe.com/reaction/1696090

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-(Di-tert-butylphosphino)biphenylHCID 2734215—
Edukt2-Methylpiperazine, (R)-HCID 7330434—
Edukt4-bromo-N-(1,2,4-thiadiazol-5-yl)benzenesulfonamideHCID 53627606—
Eduktsodium 2-methylpropan-2-olateHCID 178418730—
KatalysatorBis(dibenzylideneacetone)palladiumHCID 9811564—
LösungsmittelTolueneHCID 1140—
Produkt(r)-4-(3-Methylpiperazin-1-yl)-n-(1,2,4-thiadiazol-5-yl)benzenesulfonamideHCID 5946567419%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08163720B2
Quelldatensatzuspto-grants-2012_04
ORD IDord-fdeba54becc1465bbb3f678457cdc1a2
Quellennotizuspto-grants-2012_04