scholarly journals Retraction. One-pot synthesis of new Pyrido [2,3-d] Pyrimidine derivatives under ultrasonic irradiation using organo catalyst 4-Dimethylaminopyridine (DMAP)

2017 ◽  
Vol 4 (1) ◽  
Author(s):  
Imtiyaz Rasool Parrey ◽  
Athar Adil Hashmi
2016 ◽  
Vol 3 (1) ◽  
Author(s):  
Imtiyaz Rasool Parrey ◽  
Athar Adil Hashmi

AbstractThe one-pot synthesis of pyrido[2,3-d] pyrimidine derivatives has been reported via Knoevenagel-Michal addition pathways using substituted aromatic aldehydes, Cyanoacetamide and 6-aminouracil in N,N-dimethylformamide (DMF) solvent, with 4-dimethylaminopyridine (DMAP) as new organo catalyst catalyst under ultrasonic irradiation. The results showed that a series of aromatic aldehydes were effectively used to prepare the targeted pyrido [2, 3-d] pyrimidine derivatives with good to excellent yields (81-93 %) with no major effect on the yield of product by electron donating/withdrawing substituents. Short reaction time, environment friendly procedure, excellent yields, inexpensive and readily available catalyst are the advantages of this procedure. All synthesized compounds were characterized by IR, 1HNMR, 13CNMR and mass spectral data.


ChemInform ◽  
2005 ◽  
Vol 36 (49) ◽  
Author(s):  
Xiang-Shan Wang ◽  
Zhao-Sen Zeng ◽  
Da-Qing Shi ◽  
Shu-Jiang Tu ◽  
Xian-Yong Wei ◽  
...  

Synthesis ◽  
2018 ◽  
Vol 51 (02) ◽  
pp. 530-537 ◽  
Author(s):  
Moisés Romero-Ortega ◽  
Michelle Trujillo-Lagunas ◽  
Ignacio Medina-Mercado ◽  
Ivann Zaragoza-Galicia ◽  
Horacio Olivo

A convenient two-step, one-pot synthesis of 4-chloro-2-(trichloromethyl)pyrimidines starting from 2-(trichloromethyl)-1,3-diazabutadienes is described. These nitrogen heterocycles were prepared by a sequential acylation/intramolecular cyclization reaction between 2-(trichloromethyl)-1,3-diazabutadienes and acyl chlorides in the presence of triethylamine followed by treatment with POCl3. This is the first report for the synthesis of this type of 4-chloro-2-(trichloromethyl)pyrimidine derivatives and serves as a source for a wide variety of other substituted pyrimidines by nucleophilic substitution reactions.


Heterocycles ◽  
2017 ◽  
Vol 94 (1) ◽  
pp. 140 ◽  
Author(s):  
Kazuhiro Kobayashi ◽  
Daiki Fujiwara ◽  
Yuuho Shigemura ◽  
Hidetaka Hiyoshi ◽  
Kazuto Umezu

2019 ◽  
Vol 4 (3) ◽  
pp. 990-996
Author(s):  
Rangappa Santosh ◽  
Priyodip Paul ◽  
Mukunthan K. Selvam ◽  
Chenthattil Raril ◽  
Panchangam M. Krishna ◽  
...  

2020 ◽  
Vol 18 (26) ◽  
pp. 4971-4982 ◽  
Author(s):  
Tuan K. Nguyen ◽  
Gleb D. Titov ◽  
Olesya V. Khoroshilova ◽  
Mikhail A. Kinzhalov ◽  
Nikolai V. Rostovskii

A one-pot synthesis of tetrasubstituted dihydropyrimidine and pyrimidine derivatives was developed on the basis of UV-LED photolysis of α-azidocinnamates as a key stage.


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