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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 982613Erstellt: 25. Oktober 2026

Acrylonitrile → HCID 22562162, Verbindung

https://huagongshe.com/reaction/982613

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcrylonitrileHCID 7855—
EduktTriethylamineHCID 8471—
Edukt2,2,2-trifluoro-N-(piperidin-4-yl)acetamideHCID 10774253—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 22562162HCID 2256216230%

Reaktionsschritte

A mixture of 3 g (15.3 mmol) of 4-trifluoroacetamidopiperidine, 3 g (4.25 mL, 30.6 mmol) of triethylamine, 3 mL (45.9 mmol) of acrylonitrile in 10 mL of THF was stirred at room temperature for 17 hr. The solvent and volatile were evaporated under reduced pressure. The residue was dissolved in 20 mL of methanol and 4 mL of 30% NH4OH and the solution was refluxed for 5 hr. The solvent was evaporated under reduced pressure and the residue was purified by column chromatography on silica gel eluting first with 500 mL of dichloromethane, then 500 mL of 0.5% methanol/dichloromethane, followed by 1000 mL of 9:1:0.1 dichloromethane/methanol/ammonium hydroxide to give 0.7 g (30% yield) of the N-(2-cyanoethyl)-4-aminopiperidine. Step 4: Preparation of 6-(2-chlorophenyl)-2-(N-2-cyanoethylpiperidyl-4-amino)-pyrido[2,3-d]-pyrimidin-7-ol

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06861423B2
Quelldatensatzuspto-grants-2005_03
ORD IDord-8c3f64fbee9441ae8730b14989629cfd
Quellennotizuspto-grants-2005_03