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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1171042Generated: October 26, 2026

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

https://huagongshe.com/reaction/1171042

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Bis(aminomethyl)cyclohexaneHCID 17406—
Reactant4-Chloro-2-(2-naphthalen-1-yl-vinyl)-3,4-dihydro-quinazolineHCID 178478343—
SolventEthanolHCID 702—
Product(3-Aminomethyl-cyclohexylmethyl)-[2-(2-naphthalen-1-yl-vinyl)-quinazolin-4-yl]-amineHCID 68681390—

Reaction Steps

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;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07829566B2
Source datasetuspto-grants-2010_11
ORD IDord-3e196e30367a4ea7a3fb9a80d5c0c842
Source noteuspto-grants-2010_11