2-Phenyl-6,7-difluoro and 2-(4-fluorophenyl)quinazoline derivatives bearing salicylidenhydrazino fragments at position 4 were prepared based on 4,5-difluoroantranilic acid or anthranilamide. Molecular docking to casein kinase 2 was performed; compounds with high in silico activity CK2 revealed. Cytotoxic of the synthesized studied cancer cell line MDA-MB-231 normal WI26 VA4.

In this work, it was of interest to synthesize new series of some 2-[(E)-2-furan-2-yl-vinyl]-quinazolin-4(3H)-ones incorporated into pyrazoline, isoxazoline, pyrimidine or pyrimidine-thione ring systems at position-3 of the quinazoline ring. The antimicrobial activity and antiinflammatory effect of some of these compounds were studied.

In the compound, C(37)H(29)N(5)O(8), the quinazoline residue forms a dihedral angle of 72.90 (9)° with the triazole ring. The furan ring adopts a twist conformation. In the crystal, the mol-ecules are linked by non-classical C-H⋯N and C-H⋯O hydrogen bonds, building an infinite three-dimensional network.

The tetra-hydro-quinazoline fused-ring system of the title compound, C(11)H(10)N(2)OS, is approximately planar (r.m.s. deviation = 0.019 Å). In the crystal, adjacent mol-ecules are linked by N-H⋯O hydrogen bonds, forming a chain running along the b axis.

An unexpected copper(II)-catalyzed three-component reaction of quinazoline-3-oxide, alkylidenecyclopropane and water under mild conditions is reported. This transformation including [3+2] cycloaddition and intramolecular rearrangement leads to N-(2-(5-oxa-6-azaspiro[2.4]hept-6-en-7-yl)phenyl)formamides in good yields.

α-Enone 1, reacts with hydrazines, hydroxylamine hydrochloride, thiourea, diethylmalonate, malononitrile ethyl cyanoacetate to give the corresponding indazole, oxime, isoxazole, quinazoline, chromene and quinoline derivatives. The structures of all the synthesized compounds were confirmed by micro analytical and spectral data. The antimicrobial and the antitumor activities of some of the synthe...

In the title compound, C22H28N2, the dihedral angle between the planes of the phenyl ring and the di-hydro-quinazoline ring system (r.m.s. deviation = 0.030 Å) is 24.95 (7)° and both n-butane chains assume all-trans conformations. In the crystal, N-H⋯N hydrogen bonds link the mol-ecules into C(4) chains propagating in the [001] direction.

In the crystal structure of the title compound, C(17)H(21)N(3)O(2)·2H(2)O, water mol-ecules are mutually O-H⋯O hydrogen bonded and form infinite chains propagating along the b axis. Neighboring chains are linked by the quinazoline mol-ecules by means of O-H⋯O=C hydrogen bonds, forming a two-dimensional network.

Concurrent construction of five and six membered fused N-heretocyclic ring was achieved via a conceptually new three-component reaction affording 6,6a-dihydroisoindolo[2,1-a]quinazoline-5,11-diones as novel inhibitors of TNF-αin vitro. This represents one of the few examples of direct TNF-α inhibition by small molecules.