697297-84-0Relevant academic research and scientific papers
A simple and convenient synthesis of [1,2,4]triazolo/benzimidazolo quinazolinone and [1,2,4]triazolo[1,5-a]pyrimidine derivatives catalyzed by DABCO-based ionic liquids
Seyyedi, Narges,Shirini, Farhad,Langarudi, Mohaddeseh Safarpoor Nikoo,Jashnani, Setareh
, p. 1859 - 1867 (2017)
DABCO-based ionic liquids were utilized for the preparation of [1,2,4]triazolo/benzimidazolo quinazolinone and [1,2,4]triazolo[1,5-a]pyrimidine derivatives in the adequate procedures. These methods involve three-component reaction between aldehydes, β-dik
Preparation and characterization of a novel DABCO-based ionic liquid supported on Fe3O4@TiO2 nanoparticles and investigation of its catalytic activity in the synthesis of quinazolinones
Bakhshali-Dehkordi, Raziyeh,Ghasemzadeh, Mohammad Ali,Safaei-Ghomi, Javad
, (2020/07/06)
In this study, quinazolinone derivatives have been synthesized via a suitable and efficient procedure by one-potmulti-component reactions of 3-amino-1,2,4-triazole or 2-aminobenzimidazole, dimedone and aromatic aldehydes in the presence of Fe3O
Nanostructured γ-Fe2O3@starch-n-butyl SO3H as new recyclable magnetic catalyst for promoting multi-component reactions
Shamsi-Sani, Mahnaz,Shirini, Farhad,Mohammadi-Zeydi, Masoud
, p. 4503 - 4511 (2019/05/08)
Butane-1-soltunic acid modified starch-coated γ-Fe2O3 magnetic nanoparticles [γ-Fe2O3@starchn-butyl SO3H] was easily prepared through a ring opening reaction of 1, 4-butane sultone with nano-magnetic
Preparation of a new DABCO-based ionic liquid and investigation on its application in the synthesis of benzimidazoquinazolinone and pyrimido[4,5-b]-quinoline derivatives
Shirini, Farhad,Langarudi, Mohaddeseh Safarpoor Nikoo,Daneshvar, Nader,Mashhadinezhad, Maryam,Nabinia, Nazanin
, p. 302 - 312 (2017/08/21)
In this article, we report the preparation of a new ionic liquid from the reaction of DABCO and sulfuric acid and its characterization using FT-IR, Mass and NMR spectroscopy. This ionic liquid is air- and water-stable and affordable. Afterward this reagen
Nano-SiO2: A green, efficient, and reusable heterogeneous catalyst for the synthesis of quinazolinone derivatives
Mousavi, Mir Rasul,Maghsoodlou, Malek Taher
, p. 743 - 749 (2015/03/18)
A highly efficient and general method is applied for the multicomponent synthesis of quinazolinone derivatives from cyclocondensation of aromatic aldehydes and dimedone with 2-amino benzimidazole or 3-amino-1,2,4-triazole using nano-SiO2 as a c
A simple, economical, and environmentally benign protocol for the synthesis of [1,2,4]triazolo[5,1-b]quinazolin-8(4H)-one and hexahydro[4,5]benzimidazolo[2,1-b]quinazolinone derivatives
Mousavi, Mir Rasul,Maghsoodlou, Malek Taher,Hazeri, Nourallah,Habibi-Khorassani, Sayyed Mostafa
, p. 1419 - 1424 (2015/06/22)
Abstract An efficient synthesis of [1,2,4]triazolo[5,1-b]quinazolin-8(4H)-one and hexahydro[4,5]benzimidazolo[2,1-b]quinazolinone derivatives with good yields is described. This method involves three-component reaction between aldehydes, dimedone, and 3-a
Catalytic systems containing p-toluenesulfonic acid monohydrate catalyzed the synthesis of triazoloquinazolinone and benzimidazoquinazolinone derivatives
Mousavi, Mir Rasul,Maghsoodlou, Malek Taher
, p. 1967 - 1973 (2015/02/19)
A variety of quinazolinones are readily prepared via one-pot three-component reaction in good to excellent yields. The desired products were obtained from the reaction of dimedone, various aldehydes with 2-aminobenzimidazole or 3-amino-1,2,4-triazole unde
A simple, convenient one-pot synthesis of [1,2,4]triazolo/benzimidazolo quinazolinone derivatives by using molecular iodine
Puligoundla, Ravinder Goud,Karnakanti, Shuklachary,Bantu, Rajashaker,Nagaiah, Kommu,Kondra, Sudhakar Babu,Nagarapu, Lingaiah
, p. 2480 - 2483 (2013/06/26)
A wide variety of quinazolinone derivatives have been synthesized by condensation of 3-amino-1,2,4-triazole and 2-aminobenzimidazole as amine sources, with aromatic aldehydes and dimedone in the presence of 10 mol % of molecular iodine in acetonitrile und
