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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 600336Erstellt: 25. Oktober 2026

Potassium Carbonate → (S)-tert-Butyl 2-((S)-1-amino-3-(4'-(cyanomethyl)-3'-(methylsulfonyl)biphenyl-4-yl)-1-oxopropan-2-ylcarbamoyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/600336

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
Edukt(S)-tert-Butyl 2-((S)-1-amino-1-oxo-3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)propan-2-ylcarbamoyl)piperidine-1-carboxylateHCID 57999680—
Edukt2-(4-Bromo-2-(methylsulfonyl)phenyl)acetonitrileHCID 67269179—
KatalysatorBis(1,2-bis(diphenylphosphino)ethane)palladium(0)HCID 2724231—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt(S)-tert-Butyl 2-((S)-1-amino-3-(4'-(cyanomethyl)-3'-(methylsulfonyl)biphenyl-4-yl)-1-oxopropan-2-ylcarbamoyl)piperidine-1-carboxylateHCID 5799966876,7%

Reaktionsbedingungen

Temperatur75 °C

Reaktionsschritte

A mixture of (S)-tert-butyl 2-((S)-1-amino-1-oxo-3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)propan-2-ylcarbamoyl)piperidine-1-carboxylate (92 mg), 2-(4-bromo-2-(methylsulfonyl)phenyl)acetonitrile (75 mg), bis(1,2-bis(diphenylphosphino)ethane)-palladium(0) (8.29 mg, 9.17 μmol) and 2 N aqueous potassium carbonate (0.229 mL) in dioxane (3 mL) was heated at 75° C. for 14 h. The mixture was poured onto an Isolute HM-N cartridge, eluting with DCM, collecting about 100 mL of eluent. The eluent was concentrated in vacuo to leave a brown oil. The residue was purified by flash silica chromatography, eluting with ethyl acetate to give the subtitle compound as a white solid (80 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07902181B2
Quelldatensatzuspto-grants-2011_03
ORD IDord-5a30996f265e4b569cb305085d3cbd95
Quellennotizuspto-grants-2011_03