dimethyl 2,6-dimethyl-4-(4-nitrophenyl)-1,4-dihydropyridine-3,5-dicarb oxylate
dimethyl 2,6-dimethyl-4-(4-nitrophenyl)-1,4-dihydropyridine-3,5-dicarb oxylate Basic information
- Product Name:
- dimethyl 2,6-dimethyl-4-(4-nitrophenyl)-1,4-dihydropyridine-3,5-dicarb oxylate
- Synonyms:
-
- dimethyl 2,6-dimethyl-4-(4-nitrophenyl)-1,4-dihydropyridine-3,5-dicarb oxylate
- 1,4-dihydro-2,6-dimethyl-4-(4-nitrophenyl)-3,5-pyridinedicarboxylic acid dimethyl ester
- 3,5-Pyridinedicarboxylicacid, 1,4-dihydro-2,6-dimethyl-4-(4-nitrophenyl)-, 3,5-dimethyl ester
- Benidipine Impurity B
- Divalproex Sodium Impurity 5
- Benidipine Impurity 5 (Nifedipine Impurity 1)
- Benidipine Impurity 12
- Nifedipine Impurity 1 (Benidipine Impurity 5)
- CAS:
- 21829-09-4
- MF:
- C17H18N2O6
- MW:
- 346.33
- Mol File:
- 21829-09-4.mol
dimethyl 2,6-dimethyl-4-(4-nitrophenyl)-1,4-dihydropyridine-3,5-dicarb oxylate Chemical Properties
- Melting point:
- 165-168 °C
- Boiling point:
- 493.1±45.0 °C(Predicted)
- Density
- 1.271±0.06 g/cm3(Predicted)
- storage temp.
- 2-8°C(protect from light)
- form
- Solid
- pka
- 2.62±0.70(Predicted)
dimethyl 2,6-dimethyl-4-(4-nitrophenyl)-1,4-dihydropyridine-3,5-dicarb oxylate Usage And Synthesis
Uses
1,4-Dihydro-2,6-dimethyl-4-(4-nitrophenyl)-3,5-pyridinedicarboxylic acid dimethyl ester is used in a QSAR, diagnostic statistics and molecular modelling study among various substituted 1,?4-?dihydropyridine compounds as calcium channel antagonists.
Synthesis
555-16-8
105-45-3
21829-09-4
The general procedure for the synthesis of dimethyl 2,6-dimethyl-4-(4-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate from p-nitrobenzaldehyde and methyl acetoacetate was as follows: ammonium acetate (1 mmol) was added to a mixture of p-nitrobenzaldehyde (1 eq.) and methyl acetoacetate (1.1 eq.) in ethanol (1.5 mL) along with Er- MOF catalyst (20 mg). The reaction mixture was stirred at 70 °C for 4 hours. Upon completion of the reaction, the catalyst was removed by centrifugal separation. Subsequently, brine (5 mL) and ethyl acetate (5 mL) were added to the reaction mixture. The mixture was extracted with ethyl acetate and the organic phases were combined and washed sequentially with saturated aqueous NaHCO3 (10 mL) and brine (10 mL). The organic phase was dried over anhydrous Na2SO4 and concentrated under reduced pressure. After complete evaporation of the solvent under vacuum, the crude product was purified by column chromatography to afford the target compound dimethyl 2,6-dimethyl-4-(4-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate. The experimental results showed that the Er-MOF catalyst could be recovered and reused five times without any significant decrease in the catalytic activity.
References
[1] Chemical Communications, 2011, vol. 47, # 32, p. 9230 - 9232
[2] Tetrahedron Letters, 2010, vol. 51, # 8, p. 1187 - 1189
[3] Chemical Papers, 2011, vol. 65, # 6, p. 898 - 902
[4] Catalysis Letters, 2017, vol. 147, # 2, p. 453 - 462
[5] Patent: CN107141249, 2017, A. Location in patent: Paragraph 0130; 0131
dimethyl 2,6-dimethyl-4-(4-nitrophenyl)-1,4-dihydropyridine-3,5-dicarb oxylateSupplier
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dimethyl 2,6-dimethyl-4-(4-nitrophenyl)-1,4-dihydropyridine-3,5-dicarb oxylate(21829-09-4)Related Product Information
- Benidipine Impurity 6
- 3-benzyloxypyridine
- nifedipine iMpurity C
- Nifedipine
- 2,6-Ntp
- methyl 2,4-bis{2-nitrophenyl}-6-methyl-1,2,3,4-tetrahydro-5-pyrimidinecarboxylate
- Methyl 3-aminocrotonate
- METHYL 2-(O-NITROBENZYLIDENE)-ACETOACETATE
- Benidipine Impurity
- benidipine
- M-NIFEDIPINE
- 1-Benzyl-3-piperidinol
- Butanoic acid, 3-oxo-, 1-(phenylmethyl)-3-piperidinyl ester
- bis(1-benzylpiperidin-3-yl) 2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate
- 1,4-Dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3,5-pyridinedicarboxylic Acid 3-Methyl Ester
- Methyl 3-nitrobenzylideneacetoacetate
- benidipine
- Benidipine Impurity 15