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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 69651Erstellt: 24. Oktober 2026

Diisopropylethylamine → HCID 46864443, Verbindung

https://huagongshe.com/de/reaction/69651

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
Edukt1-(4-Chlorophenyl)piperazine HydrochlorideHCID 3084720—
Edukt(Cyanomethyl)trimethylphosphanium iodideHCID 10514344—
Edukt4-benzyl-7-(hydroxymethyl)-3,4-dihydropyrido[2,3-b]pyrazin-2(1H)-oneHCID 58324463—
LösungsmittelWaterHCID 962—
LösungsmittelPropionitrileHCID 7854—
ProduktHCID 46864443HCID 4686444340,2%

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

4-benzyl-7-(hydroxymethyl)-3,4-dihydropyrido[2,3-b]pyrazin-2(1H)-one (100 mg, 0.37 mmol) was suspended in propionitrile (1 mL) and (cyanomethyl)trimethylphosphonium iodide (123.0 mg, 0.51 mmol) was added followed by N-ethyl-N-isopropylpropan-2-amine (180 ul, 1.03 mmol). To the stirred mixture was then added 1-(4-chlorophenyl)piperazine hydrochloride (104.5 mg, 0.45 mmol). The reaction was heated to 90° C. with stirring for 2 h. The reaction was then cooled to room temperature and diluted with water (3 mL) and filtered. The solids were collected and refluxed in ethanol (5 mL) for 1 h. The suspension was cooled back to room temperature and filtered. The precipitate was filtered off and dried in vacuum to afford the title compound (66.6 mg, 40%) as a white solid. 1H NMR (DMSO-d6) δ (ppm): 10.57 (s, 1H), 7.64 (d, J=1.8 Hz, 1H), 7.33 (d, J=4.5 Hz, 4H), 7.25-7.30 (m, 1H), 7.19-7.24 (m, 2H), 7.01 (d, J=1.8 Hz, 1H), 6.92 (d, J=9.1 Hz, 2H), 4.72 (s, 2H), 3.86 (s, 2H), 3.36 (s, 2H), 3.07-3.15 (m, 4H), 2.44-2.49 (m, 4H). [M+H] calc'd for C25H26ClN5O, 448; found, 448.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08822470B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-5bb20f10cdef4c5687f2b0f876d1984f
Quellennotizuspto-grants-2014_09