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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1193398Erstellt: 25. Oktober 2026

Binap, (A+-)- → HCID 66799007, Verbindung

https://huagongshe.com/reaction/1193398

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBinap, (A+-)-HCID 634876—
Edukt4-N-Boc-4-N-Methyl-aminopiperidineHCID 2756806—
Edukt2-Chloro-6-methylpyrazineHCID 7170095—
KatalysatorBis(dibenzylideneacetone)palladiumHCID 9811564—
LösungsmittelTolueneHCID 1140—
ProduktHCID 66799007HCID 6679900747%

Reaktionsschritte

KOBut (483 mg, 4.32 mmol, 2.5 eq) was added at room temperature to a solution of tert-butyl methyl(piperidin-4-yl)carbamate (stage 3 AMN-60) (370 mg, 1.72 mmol, 1 eq) and 2-chloro-6-methylpyrazine (244 mg, 1.9 mmol, 1.1 eq) in toluene (50 ml) and the mixture was degassed for 30 min with argon. BINAP (64.5 mg, 0.103 mmol, 0.06 eq) and Pd2(dba)3 (31.6 mg, 0.034 mmol, 0.02 eq) were added and the reaction mixture was refluxed for 16 h. After cooling, concentration under reduced pressure was carried out. The residue was taken up in dichloromethane (50 ml) and washed with water (30 ml) and saturated sodium chloride solution (30 ml) and dried over sodium sulfate. The solvent was removed by distillation under reduced pressure and the crude product so obtained was purified by column chromatography (Alox, 0.5% methanol/dichloromethane). The desired product was in the form of a brown solid. Yield: 47% (250 mg, 0.816 mmol)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08680159B2
Quelldatensatzuspto-grants-2014_03
ORD IDord-a1044dc86d6d4014993a32f2ef429826
Quellennotizuspto-grants-2014_03