21835-70-1

Upstream product

• 105-45-3 acetoacetic acid methyl ester 
• 100-10-7 4-dimethylamino-benzaldehyde 

Downstream Products

• 66941-31-9 4-(3,5-bis-methoxycarbonyl-2,6-dimethyl-1,4-dihydro-[4]pyridyl)-N-butyl-N,N-dimethyl-anilinium; iodide 
• 100353-94-4 4-(3,5-bis-methoxycarbonyl-2,6-dimethyl-1,4-dihydro-[4]pyridyl)-N,N-dimethyl-N-propyl-anilinium; iodide 
• 66941-34-2 4-(3,5-bis-methoxycarbonyl-2,6-dimethyl-1,4-dihydro-[4]pyridyl)-tri-N-methyl-anilinium; iodide 

Relevant academic research and scientific papers

Synthesis and application of chitosan supported vanadium oxo in the synthesis of 1,4-dihydropyridines and 2,4,6-triarylpyridines: Via anomeric based oxidation

Chitosan, as a biopolymer, exhibits a strong affinity for complexation with suitable metal ions. Thus, it has received increased attention for the preparation of stable bioorganic-inorganic hybrid heterogeneous catalysts. Herein, a novel chitosan based vanadium oxo (ChVO) catalyst was prepared and fully characterized by several techniques such as Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), thermal gravimetric analysis (TGA), derivative thermal gravimetric (DTG), differential thermal analysis (DTA), scanning electron microscopy (SEM), energy dispersive X-ray analysis (EDX), high-resolution transmission electron microscopy (HRTEM), selected area electron diffraction (SAED), X-ray photoelectron spectroscopy (XPS) and inductively coupled plasma mass spectrometry (ICP-MS). The synthesized catalyst has been successfully used as a reusable catalyst in the synthesis of dihydropyridines and triarylpyridines.

Comparative study of various green chemistry approaches for the efficient synthesis of 1,4-dihydropyridines

Hantzsch 1,4-dihydropyridine and its derivatives are an important class of bioactive molecules in the pharmaceutical field. The work on this project was started with the objective of synthesizing known 1,4-dihydropyridine by various green chemistry methods like microwave, solvent-free, ultrasonication and compared the results with conventional technique using different aldehydes and 1,3-dicarbonyl compounds as substituents. The twelve known 1,4-dihydropyridines were synthesized and characterized by their TLC, FT-IR and 1H NMR, elemental studies. When all the data cross-examined, it was concluded that microwave, ultrasonic and solvent-free methods were efficient and less time consuming with high yield. At the same time conventional method was time consuming but scalable when compared with other methods.

Barium nitrate catalyzed one pot synthesis of 1,4-dihydropyridines under solvent free conditions at room temperature

(Chemical Equation Presented) Barium nitrate acts as an efficient catalyst for the three-component one pot synthesis of 1,4-dihydropyridines. Barium nitrate is a safe chemical, and reaction without the use of organic solvents makes the process eco-friendly.

PROCESS FOR THE PREPARATION OF 1,4-DIHYDROPYRIDINES AND NOVEL 1,4-DIHYDROPYRIDINES USEFUL AS THERAPEUTIC AGENTS

The present invention provides a process for the preparation of 1,4-dihydropyridines of the formula (1), wherein R1 is H, NO2, Cl, OAc, OH, R2 is H, NO2, Cl, -O-CH2-O-, OMe, OAc, OEt, OH, R3 is H, NO2, Cl, N(Me)2, -O- CH2 -O-, OMe, OAc, OH, R4 is H, OMe, OAc, OH, R5 is H, Cl, I, and R6 and R7 are either methyl, ethyl or both by preparing a mixture of an aromatic aldehyde, alkyl acetoacetate and a source of ammonia, adsorbing the prepared mixture and adsorbent till adsorbent becomes free flowing, heating the material so obtained under microwave irradiation, cooling the reaction mixture and recovering the compound of formula (1). The present invention also relates to novel 1,4-dihydropyridines with cardiovascular activity.

1,4-Dihydropyridine antagonist activities at the calcium channel: A quantitative structure-activity relationship approach

The effect of 46 1,4-dihydropyridine-type calcium channel antagonists on the tonic contractile response of longitudinal muscle strips of guinea pig ileum was determined. 2,6-Dimethyl-3,5-dicarbomethoxy-4-phenyl-1,4-dihydropyridine (13) and 13 ortho-, 15 meta-, and seven para-monosubstituted and 10 polysubstituted aromatic derivatives of 13 were studied. The pharmacological activities of the monosubstituted derivatives were best correlated by eq 10, log 1/C = 0.68π + 2.50σ(m) - 0.47L(meta) - 3.40B1(para) + 11.31, which had a correlation coefficient of 0.89. The full data set was best correlated by eq 11, log 1/C = 0.62π + 1.96σ(m) - 0.44L(meta) - 3.26B1(para) - 1.51L(meta) + 14.23, which had a correlation coefficient of 0.90. Equations of similar form but involving an ortho steric term were found to correlate the radioligand binding data for this class of compounds.