5-(Methoxycarbonyl)-2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3-carboxylic acid synthesis
- Product Name:5-(Methoxycarbonyl)-2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3-carboxylic acid
- CAS Number:74936-72-4
- Molecular formula:C16H16N2O6
- Molecular Weight:332.31
21881-77-6
74936-72-4
General procedure for the synthesis of monomethyl 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-4-(3-nitrophenyl)pyridine-3,5-dicarboxylate from dimethyl 2,6-dimethyl-4-(3-nitrophenyl)pyridine-3,5-dicarboxylate: (3) Preparation of 5-methoxycarbonyl-2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3-carboxylic acid Dimethyl 2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate (0.01 mol) was mixed with 150 mL of methanol. Saturated aqueous NaOH solution (9 g, 0.225 mol) was slowly added to the mixture under stirring conditions. The reaction mixture was vigorously stirred at 70 °C for 6 hours. Upon completion of the reaction, about 80 mL of methanol was removed by evaporation under reduced pressure. 200 mL of water was added to the residue and unreacted feedstock was removed by filtration. The filtrate was adjusted to pH about 2.5 with 1 mol/L hydrochloric acid, at which point a yellow solid precipitated, which was filtered and dried to give a khaki colored powder. The resulting powder was recrystallized from methanol to give the title product 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)pyridine-3,5-dicarboxylic acid monomethyl ester as a yellow solid (1.9 g, 57.2% yield).
75130-24-4
38 suppliers
inquiry
74936-72-4
262 suppliers
$15.00/5g
Yield:74936-72-4 86.8%
Reaction Conditions:
with water;sodium hydroxide at 20;Reagent/catalyst;
Steps:
1.3; 2.3
(3) Intermediate 2 (1800g),750 g of a 3% aqueous sodium hydroxide solution was added to the reaction.The reaction is carried out at room temperature for 2 to 3 hours; and then extracted with 10000 g of dichloromethane;The aqueous phase was acidified to pH = 1-2 with 10% hydrochloric acid. Filtered, dried,It has a pale yellow solid. The obtained solid was recrystallized from methanol to give Intermediate 3 (1346 g).The yield was 86.8%.
References:
CN109111431,2019,A Location in patent:Paragraph 0042; 0046; 0056; 0060
21881-77-6
130 suppliers
$8.00/1g
74936-72-4
262 suppliers
$15.00/5g
21881-77-6
130 suppliers
$8.00/1g
7440-44-0
369 suppliers
$12.00/25g
74936-72-4
262 suppliers
$15.00/5g
541-50-4
58 suppliers
inquiry
99-61-6
651 suppliers
$5.00/10g
14205-39-1
511 suppliers
$6.00/25g
74936-72-4
262 suppliers
$15.00/5g
99-61-6
651 suppliers
$5.00/10g
74936-72-4
262 suppliers
$15.00/5g