2010
DOI: 10.1080/17518251003749353
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Novel pyrimidine derivatives by sonication and traditional thermal methods

Abstract: A series of bis-compounds (2) were synthesized by condensing dihydro-1,3-(disubstituted)phenyl-2-thioxopyrimidine-4,6(1H,5H)-dione with hippuric acid in presence of acetic anhydride. The compound (2) on further treatment with aromatic amine afforded dihydropyrimidine (3) through an eco-friendly procedure by sonication. The sonication method reduces time and gives higher yields, and also the effluent produced is free from hazardous contamination and organic by-products. The novel pyrimidines were also synthesiz… Show more

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Cited by 38 publications
(12 citation statements)
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“…According to Table 3, the aryl aldehydes with electronwithdrawing groups, such as NO 2 and Cl, in p-position reacted with 2-aminobenzothiazole, dimethyl acetylenedicarboxylate and morpholine/piperidine very smoothly, while the reactants with electron-donating groups, such as hydroxy and methoxy, proceeded with the longer reaction time along with the lower product yields. In addition, the sterically hindered aldehydes reacted more slowly in comparison with the unhindered ones.…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…According to Table 3, the aryl aldehydes with electronwithdrawing groups, such as NO 2 and Cl, in p-position reacted with 2-aminobenzothiazole, dimethyl acetylenedicarboxylate and morpholine/piperidine very smoothly, while the reactants with electron-donating groups, such as hydroxy and methoxy, proceeded with the longer reaction time along with the lower product yields. In addition, the sterically hindered aldehydes reacted more slowly in comparison with the unhindered ones.…”
Section: Resultsmentioning
confidence: 99%
“…Furthermore, MCRs are easy to perform, inexpensive, quick, energy efficient and experimental procedures are relatively simple (1). Recently, the application of ultrasonic irradiation in chemical syntheses has received much attention (2)(3)(4)(5). On the other hand, designing MCRs under ultrasonic irradiation is another attractive area in synthetic organic chemistry.…”
Section: Introductionmentioning
confidence: 99%
“…For all these reasons, the various possibilities offered by the microwave technology are particularly attractive where fast, high-yielding protocols and the avoidance or facilitation of purification are highly desirable. [5][6] Wherever domestic microwave oven, which do not provide a scientifically adequate level of reproducibility, was used by the authors is mentioned in the present paper.…”
Section: Introductionmentioning
confidence: 99%
“…In many cases, the classic syntheses provide reliable access to heterocyclic compounds; however, they are simply no longer acceptable by current environmental and safety standards. For all these reasons, the various possibilities offered by the microwave technology are particularly attractive where fast, high‐yielding protocols and the avoidance or facilitation of purification are highly desirable . Wherever a domestic microwave oven, which does not provide a scientifically adequate level of reproducibility, was used by the authors is mentioned in the present article.…”
Section: Introductionmentioning
confidence: 99%