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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 333909Erstellt: 24. Oktober 2026

Dimethylformamide → (S)-6-(2-Hydroxy-2-methyl-propyl)-3-{(S)-1-[4-(1-methyl-2-oxo-1,2-dihydro-pyridin-4-ylethynyl)-phenyl]ethyl}-6-phenyl-[1,3]oxazinan-2-one

https://huagongshe.com/de/reaction/333909

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktTriethylamineHCID 8471—
Edukt4-Bromo-1-methylpyridin-2(1H)-oneHCID 22132396—
Edukt(S)-3-((S)-1-(4-ethynylphenyl)ethyl)-6-(2-hydroxy-2-methylpropyl)-6-phenyl-1,3-oxazinan-2-oneHCID 86670541—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
KatalysatorHCID 178418476HCID 178418476—
LösungsmittelWaterHCID 962—
Produkt(S)-6-(2-Hydroxy-2-methyl-propyl)-3-{(S)-1-[4-(1-methyl-2-oxo-1,2-dihydro-pyridin-4-ylethynyl)-phenyl]ethyl}-6-phenyl-[1,3]oxazinan-2-oneHCID 66869817—

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

CuI (68 mg), Pd(PPh3)2Cl2 (125 mg), and NEt3 (0.82 mL) were added successively to a flask charged with a stir bar, 4-bromo-1-methyl-1H-pyridin-2-one (0.38 g), 3-[(S)-1-(4-ethynyl-phenyl)-ethyl]-(S)-6-(2-hydroxy-2-methyl-propyl)-6-phenyl-[1,3]oxazinan-2-one (0.61 g), and N,N-dimethylformamide (3 mL) and kept at room temperature under argon atmosphere. The resulting mixture was heated to 100° C. and stirred at this temperature for 4 h. After cooling the mixture to ambient temperature, water was added and the resulting mixture was extracted with ethyl acetate. The combined organic extracts were washed with water and brine and dried (MgSO4). The solvent was evaporated and the residue was chromatographed on silica gel twice (first chromatography: ethyl acetate/methanol 1:0->4:1; second chromatography: dichloromethane/methanol 19:1->9:1) to afford the title compound as an oil which crystallized from ethyl acetate. Yield: 0.27 g (34% of theory); LC-MS (Method 1): tR=3.41 min; Mass spectrum (ESI+): m/z=485 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08883778B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-8737c493692d403fb7d6f6ec83060ed2
Quellennotizuspto-grants-2014_11