Synthesis and structure of novel 4-arylhexahydro-1H,3H-pyrido[1,2-c]pyrimidine derivatives
✍ Scribed by Franciszek Herold; Ewa Helbin; Marek Król; Irena Wolska; Jerzy Kleps
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 1999
- Tongue
- English
- Weight
- 514 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0022-152X
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✦ Synopsis
Abstract
A series of new 4‐aryl‐hexahydro‐1__H__,3__H__‐pyrido[1,2‐c]pyrirnidine‐1,3‐dione derivatives 4a‐k were prepared by catalytic hydrogenation of 4‐aryl‐1__H__,2__H__‐pyrido[1,2‐c]pyrirnidine‐1,3‐diones 3a‐k. The structures of compounds were determined by ^1^H and ^13^C nmr spectroscopy in solution. Steric hindrance caused twisting of the phenyl ring with respect to the pyridopyrimidine system, the effect was confirmed by X‐ray diffraction.
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## 13 C cross-polarization magic angle spinning NMR data are reported for eight derivatives of 4-arylhexahydro-1H,3H-pyrido[1,2-c]pyrimidine-1,3-diones 1-8 and the x-ray diffraction data for 4 with R = 4'-Me. The crystal structure of 4 shows the formation of centrosymmetric dimers via intermolecul
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
## Abstract A series of new 4‐aryloctahydropyrido[1,2‐__c__]pyrimidine‐1,3‐diones **6a,b,d‐h** and **j** were synthesized by intramolecular cyclization of α‐aryl‐α‐(1‐ethoxycarbonyl‐2‐piperidyl)‐acetamide derivatives **5a,b,d‐h** and **j**. The structures of compounds were determined by ^1^H and ^1
## Abstract For Abstract see ChemInform Abstract in Full Text.