Results 81 to 90 of about 24,434,811 (177)

Synthesis of Quinazoline and Quinazolinone Derivatives via Ligand-Promoted Ruthenium-Catalyzed Dehydrogenative and Deaminative Coupling Reaction of 2‑Aminophenyl Ketones and 2‑Aminobenzamides with Amines [PDF]

open access: yes, 2019
The in situ formed ruthenium catalytic system ([Ru]/L) was found to be highly selective for the dehydrogenative coupling reaction of 2-aminophenyl ketones with amines to form quinazoline products.
Chae S. Yi   +5 more
core   +1 more source

Exploring Quinazoline Nitro-Derivatives as Potential Antichagasic Agents: Synthesis and In Vitro Evaluation

open access: yesMolecules
Trypanosoma cruzi is a protozoan parasite that causes Chagas disease in humans. The current antichagasic drugs nifurtimox and benznidazole have inconveniences of toxicity; therefore, the search for alternative therapeutic strategies is necessary.
Citlali Vázquez   +7 more
doaj   +1 more source

Synthesis of 3-[2-(1H-imidazol-2-yl)alkyl]-2-thioxo-2,3-dihydroquinazolin-4(1H)-one derivatives

open access: yesAktualʹnì Pitannâ Farmacevtičnoï ì Medičnoï Nauki ta Praktiki, 2018
Promising biologically active substances are derivatives of imidazole and quinazoline, which are part of the structure of known antifungal drugs and substances with anti-TB and antimicrobial activity.
O. A. Zavada   +2 more
doaj   +1 more source

The preparation and reactivity of some potassium Purine-, Quinazoline-, and Tetrahydroquinazoline-sulphonates

open access: yes, 1972
The potassium salts of purine-6(and 8)-, 9-methylpurine-6-, quinazoline-2(and 4)-, 5,6,7,8-tetrahydroquinazoline-4-, and 5,6,7,8- tetrahydro-2-methylquinazoline-4-sulphonic acid are prepared by treatment of the corresponding thiones with aqueous ...
DJ Brown, JA Hoskins
core   +1 more source

Synthesis of Quinazoline Derivatives

open access: yes
Efficient synthesis of heterocyclic has always been a very important task in drug discovery. Most of the drugs contain heterocycles to provide an interface between chemistry and biology.
Yadav, Anjali   +5 more
core   +1 more source

2,5-Dimethyl-6,7-dihydrobenzo[h]-pyrazolo[1,5-a]quinazoline and 2-tert-butyl-5-methyl-6,7-dihydrobenzo[h]-pyrazolo[1,5-a]quinazoline

open access: yes, 2007
In both 2,5- dimethyl- 6,7- dihydrobenzo[ h] pyrazolo[ 1,5- a]quinazoline, C16H15N3, ( I), and 2- tert- butyl- 5- methyl- 6,7dihydrobenzo[ h] pyrazolo[ 1,5- a] quinazoline, C19H21N3, ( II), which crystallizes with Z' = 2 in the space group P1, the ...
Portilla, Jaime   +4 more
core   +1 more source

Structure-based rational design and biological evaluation of a quinazoline-based EGFR exon 20 insertion inhibitor

open access: yesJournal of Enzyme Inhibition and Medicinal Chemistry
This study describes the structure-based design and synthesis of potent quinazoline-based inhibitors targeting EGFR exon 20 insertion (exon20ins) mutants, one of the challenging oncogenic drivers in non-small cell lung cancer (NSCLC). Guided by in silico
Sooheum Jo   +3 more
doaj   +1 more source

6-(2-Fluorophenyl)-5,6-dihydrobenzimidazolo[1,2-c]quinazoline

open access: yesActa Crystallographica Section E, 2008
In the title compound, C20H14FN3, the pyrimidine ring adopts a half-chair conformation. The dihedral angle between the benzimidazole ring system and the fluorophenyl ring is 84.18 (10)°.
Ai-Ke Li   +4 more
doaj   +1 more source

Synthesis of 6-acrylamido-4-(2-[18F]fluoroanilino)quinazoline: Aprospective irreversible EGFR binding probe [PDF]

open access: yes, 2004
Acrylamido-quinazolines substituted at the 6-position bindirreversibly to the intracellular ATP binding domain of the epidermalgrowth factor receptor (EGFR).
Nandanan,Erathodiyil   +7 more
core  

Quinazoline derivatives: synthesis and bioactivities

open access: yes, 2013
Owing to the significant biological activities, quinazoline derivatives have drawn more and more attention in the synthesis and bioactivities research. This review summarizes the recent advances in the synthesis and biological activities investigations ...
Wang, Dan, Feng Gao, Gao, Feng, Dan Wang
core   +1 more source

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