Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1432976Erstellt: 25. Oktober 2026

1-(4-Aminoquinazoline-7-ylmethyl)-3-propyl-piperazine-2-one → 4-[3-(6-Amino-pyridin-3-yl)-acryloyl]-1-(4-amino-quinazolin-7-ylmethyl)-3-(S)-propyl-piperazin-2-one

https://huagongshe.com/reaction/1432976

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-(4-Aminoquinazoline-7-ylmethyl)-3-propyl-piperazine-2-oneHCID 17985268—
Edukt3-(6-Aminopyridin-3-yl)prop-2-enoic acidHCID 53400832—
Produkt4-[3-(6-Amino-pyridin-3-yl)-acryloyl]-1-(4-amino-quinazolin-7-ylmethyl)-3-(S)-propyl-piperazin-2-oneHCID 54266617—

Reaktionsschritte

The title compound is prepared as described in EXAMPLE 123, using 1-(4-aminoquinazoline-7-ylmethyl)-3-propyl-piperazine-2-one, EXAMPLE 78 and 3-(6-amino-pyridin-3-yl)-acrylic acid, EXAMPLE 36. 1H NMR (d6-DMSO, 300 MHz) δ9.73 (bs, 2H), 8.81 (s, 1H), 8.36 (m, 2H), 8.22 (m, 3H), 7.62 (d, 1H), 7.52 (m, 1H), 7.39 (m, 1H), 7.21 (m, 1H), 6.91 (d, 1H), 5.00 (m, 1H), 4.78 (m, 1H), 4.60 (m, 2H), 4.34 (m, 1H), 3.30 (m, 2H), 1.87 (m, 2H), 1.24 (m, 2H), 0.90 (m, 3H). MS (ion spray), m/z, 446, 448 (M+H), (Cl pattern).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07612075B2
Quelldatensatzuspto-grants-2009_11
ORD IDord-3387d366f278447091e4626fcffa3728
Quellennotizuspto-grants-2009_11