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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1499102Erstellt: 26. Oktober 2026

N-((1R,2R)-2-Amino-1,2-diphenylethyl)-4-methylbenzene-1-sulfonamide → HCID 117942080, Verbindung

https://huagongshe.com/reaction/1499102

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-((1R,2R)-2-Amino-1,2-diphenylethyl)-4-methylbenzene-1-sulfonamideHCID 2734565—
EduktPotassium FormateHCID 2735122—
Edukt1-(4-Bromo-2-(3-methyl-1H-pyrazol-1-yl)phenyl)-2,2,2-trifluoroethanoneHCID 117942112—
KatalysatorHCID 178477776HCID 178477776—
LösungsmittelWaterHCID 962—
LösungsmittelAcetonitrileHCID 6342—
ProduktHCID 117942080HCID 117942080—

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

Pentamethylcyclopentadienyl iridium (III) chloride dimer (CAS#12354-84-6) (10.4 mg) and (1R,2R)-(−)-N-(4-toluene sulfonyl)-1,2-diphenyl ethylene diamine (CAS#144222-34-4) (9.2 mg) were combined in water (120 mL), then heated to 50° C. for 5 h to provide the “Iridium complex.” 1-[4-Bromo-2-(3-methyl-1H-pyrazol-1-yl)phenyl]-2,2,2-trifluoroethanone (16 g, 48 mmol) was dissolved in acetonitrile (120 mL) to which the Iridium complex and potassium formate (3.1 g, 3.7 mmol) were added. The reaction mixture was heated to 50° C. for 8 h. The reaction mixture was then cooled to RT, partitioned between water and EtOAc, and extracted. The combined organic layers were washed with brine, dried over Na2SO4, filtered, and concentrated in vacuo. Recrystallization from hot heptane (200 mL) provided the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09199994B2
Quelldatensatzuspto-grants-2015_12
ORD IDord-89e44f85a3e4496ca1b80e58d5cb93fa
Quellennotizuspto-grants-2015_12