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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | N-((1R,2R)-2-Amino-1,2-diphenylethyl)-4-methylbenzene-1-sulfonamide | HCID 2734565 | — |
| Edukt | Potassium Formate | HCID 2735122 | — |
| Edukt | 1-(4-Bromo-2-(3-methyl-1H-pyrazol-1-yl)phenyl)-2,2,2-trifluoroethanone | HCID 117942112 | — |
| Katalysator | HCID 178477776 | HCID 178477776 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | HCID 117942080 | HCID 117942080 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US09199994B2 |
|---|
| Quelldatensatz | uspto-grants-2015_12 |
|---|
| ORD ID | ord-89e44f85a3e4496ca1b80e58d5cb93fa |
|---|
| Quellennotiz | uspto-grants-2015_12 |
|---|