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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 716044Erstellt: 25. Oktober 2026

2-Cyano-N,N-dimethylacetamide → 2-cyano-N,N-dimethyl-3-(6-(7-pivaloyl-5-((2-(trimethylsilyl)ethoxy)methyl)-5H-pyrrolo[2,3-b]pyrazin-2-ylamino)pyridin-3-yl)acrylamide

https://huagongshe.com/reaction/716044

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Cyano-N,N-dimethylacetamideHCID 251143—
EduktPiperidine, acetateHCID 9793820—
EduktHCID 86712128HCID 86712128—
LösungsmittelEthanolHCID 702—
Produkt2-cyano-N,N-dimethyl-3-(6-(7-pivaloyl-5-((2-(trimethylsilyl)ethoxy)methyl)-5H-pyrrolo[2,3-b]pyrazin-2-ylamino)pyridin-3-yl)acrylamideHCID 7101429588,8%

Reaktionsschritte

To a 50 ml three necked round bottom flask 6-(7-pivaloyl-5-((2-(trimethylsilyl)-ethoxy)methyl)-5H-pyrrolo[2,3-b]pyrazin-2-ylamino)-nicotinaldehyde (0.33 g, 0.00072 mole) and 2-cyano-N,N-dimethylacetamide (0.245 g, 0.00218 mole) was taken in ethanol (10 ml). To this reaction mixture, piperidine acetate (3.3 M solution in water) (0.1 ml) was added drop wise at RT. After completion of the addition, reaction mixture was refluxed for 4 hrs. After completion of the reaction, the ethanol was distilled out and water was added to residue. The aqueous layer was extracted with ethyl acetate and organic layers were combined, dried over Na2SO4, filtered and concentrated to afford crude product. The crude compound was purified by triturated with n-pentane (10.0 ml), pentane layer was decanted and solid was dried under vacuum to yield 0.35 g of 2-cyano-N,N-dimethyl-3-(6-(7-pivaloyl-5-((2-(trimethylsilyl)ethoxy)methyl)-5H-pyrrolo[2,3-b]pyrazin-2-ylamino)pyridin-3-yl)acrylamide.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09187487B2
Quelldatensatzuspto-grants-2015_11
ORD IDord-dcc2c1e7086c4eee8414f77f3a5b1caa
Quellennotizuspto-grants-2015_11