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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1171042Erstellt: 27. Oktober 2026

1,3-Bis(aminomethyl)cyclohexane → (3-Aminomethyl-cyclohexylmethyl)-[2-(2-naphthalen-1-yl-vinyl)-quinazolin-4-yl]-amine

https://huagongshe.com/reaction/1171042

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,3-Bis(aminomethyl)cyclohexaneHCID 17406—
Edukt4-Chloro-2-(2-naphthalen-1-yl-vinyl)-3,4-dihydro-quinazolineHCID 178478343—
LösungsmittelEthanolHCID 702—
Produkt(3-Aminomethyl-cyclohexylmethyl)-[2-(2-naphthalen-1-yl-vinyl)-quinazolin-4-yl]-amineHCID 68681390—

Reaktionsschritte

4-Chloro-2-(2-naphthalen-1-yl-vinyl)-3,4-dihydro-quinazoline (0.08 mmol), C-(3-aminomethyl-cyclohexyl)-methylamine (0.24 mmol) and 2 ml ethyl alcohol are placed in an 8 ml glass vial sealed with a teflon-lined screw cap. The mixture is heated at 80° for 3 hrs. After cooling to rt, the ethyl alcohol is removed. Ethyl acetate (3 ml) and water (3 ml) are added to the vial. After agitation, the water was removed. The procedure is repeated with water and aq. NaCl (sat.). Purification with silica gel afforded (3-aminomethyl-cyclohexylmethyl)-[2-(2-naphthalen-1-yl-vinyl)-quinazolin-4-yl]-amine;

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07829566B2
Quelldatensatzuspto-grants-2010_11
ORD IDord-3e196e30367a4ea7a3fb9a80d5c0c842
Quellennotizuspto-grants-2010_11