Synthesis, structural elucidation and pharmacological properties of some 5-acetyl-3,4-dihydro-6-methyl-4-(substituted phenyl)-2(1H)-pyrimidinones
-
Add time:08/10/2019 Source:sciencedirect.com
In this study, the synthesis of some new 5-acetyl-3,4-dihydro-6-methyl-4-(substituted phenyl)-2(1H)-pyrimidinones has been reported. The compounds were prepared by the Biginelli reaction of acetylacetone with aromatic aldehydes and urea. The structures of the compounds were characterized by UV, IR, 1H NMR, 13C NMR, mass spectra and elementary analysis. The calcium antagonistic activity of these compounds was tested in vitro on rat ileum precontracted with 4×10−3 M barium chloride.
We also recommend Trading Suppliers and Manufacturers of 6-METHYL-2-PHENYL-4(1H)PYRIMIDINONE (cas 13514-79-9). Pls Click Website Link as below: cas 13514-79-9 suppliers
Prev:Identification of 2(1H)-pyrimidinones as potential EGFR T790M inhibitors for the treatment of gefitinib-resistant non-small cell lung cancer
Next:Direct regioselective Csp2–H trifluoromethylation of pyrimidinones and pyridinones) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- A click-generated triazole tethered oxazolone-pyrimidinone dyad: A highly selective colorimetric and ratiometric FRET based fluorescent probe for sensing azide ions08/14/2019
- Pentafluorophenylammonium triflate (PFPAT) catalyzed facile construction of substituted chromeno[2,3-d]pyrimidinone derivatives and their antimicrobial activity08/13/2019
- Synthesis of fluorinated pyrimidinones08/12/2019
- Direct regioselective Csp2–H trifluoromethylation of pyrimidinones and pyridinones08/11/2019
- Identification of 2(1H)-pyrimidinones as potential EGFR T790M inhibitors for the treatment of gefitinib-resistant non-small cell lung cancer08/09/2019


