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72509-76-3

Basic Information
CAS No.: 72509-76-3
Name: Felodipine
Article Data: 21
Molecular Structure:
Molecular Structure of 72509-76-3 (Felodipine)
Formula: C18H19Cl2NO4
Molecular Weight: 384.259
Synonyms: Hydac;Munobal;Plendil;Prevex;Splendil;dl-Felodipine;3,5-Pyridinedicarboxylicacid, 4-(2,3-dichlorophenyl)-1,4-dihydro-2,6-dimethyl-, ethyl methyl ester(9CI);Agon;Delmuno;Feloday;Flodil;H 154/82;
EINECS: 620-472-7
Density: 1.277 g/cm3
Melting Point: 142-145 °C
Boiling Point: 471.5 °C at 760 mmHg
Flash Point: 239 °C
Solubility: insoluble in water
Appearance: White or light yellow crystalline powder
Hazard Symbols: HarmfulXn
Risk Codes: 22
Safety: 36
PSA: 64.63000
LogP: 4.29310
Synthetic route
68064-64-2, 94739-24-9, 68064-63-1

2-<(2,3-dichlorophenyl)methylene>-3-oxobutanoic acid ethyl ester

21731-17-9

methyl 3-aminocrotonate

72509-76-3

ethyl methyl 1,4-dihydro-2,6-dimethyl-4(2,3-dichlorophenyl)-3,5-pyridinedicarboxylate

Conditions
ConditionsYield
In ethanol for 0.075h; Irradiation; Teflon vessel, microwave oven;96%
626-34-6

ethyl 3-aminobut-2-enoate

105-45-3

acetoacetic acid methyl ester

6334-18-5

2,3-dichlorobenzylaldehyde

72509-76-3

ethyl methyl 1,4-dihydro-2,6-dimethyl-4(2,3-dichlorophenyl)-3,5-pyridinedicarboxylate

Conditions
ConditionsYield
Stage #1: ethyl 3-aminobut-2-enoate; acetoacetic acid methyl ester; 2,3-dichlorobenzylaldehyde With piperidine; pyridine In neat (no solvent) at 75 - 80℃; for 9h;
Stage #2: With ethanol for 1h; Reagent/catalyst; Solvent; Reflux;
94.3%

ethyl aminocrotonate

68064-69-7

(Z)-methyl 2-(2,3-dichlorobenzylidene)-3-oxobutanoate

72509-76-3

ethyl methyl 1,4-dihydro-2,6-dimethyl-4(2,3-dichlorophenyl)-3,5-pyridinedicarboxylate

Conditions
ConditionsYield
In isopropyl alcohol for 12h; Heating / reflux;86%
1352187-23-5

C33H34Cl2N2O7S

124-41-4

sodium methylate

72509-76-3

ethyl methyl 1,4-dihydro-2,6-dimethyl-4(2,3-dichlorophenyl)-3,5-pyridinedicarboxylate

Conditions
ConditionsYield
In methanol chemoselective reaction;84%
68064-64-2, 94739-24-9, 68064-63-1

2-<(2,3-dichlorophenyl)methylene>-3-oxobutanoic acid ethyl ester

81777-30-2

1,1,1-Triphenyl-3-methyl-4-(methoxycarbonyl)-2-aza-1λ5-phosphabuta-1,3-diene

72509-76-3

ethyl methyl 1,4-dihydro-2,6-dimethyl-4(2,3-dichlorophenyl)-3,5-pyridinedicarboxylate

Conditions
ConditionsYield
In dichloromethane at 40℃; for 24h;82%

4-(2,3-Dichloro-phenyl)-2,6-dimethyl-1,4-dihydro-pyridine-3,5-dicarboxylic acid monoethyl ester

74-88-4

methyl iodide

72509-76-3

ethyl methyl 1,4-dihydro-2,6-dimethyl-4(2,3-dichlorophenyl)-3,5-pyridinedicarboxylate

Conditions
ConditionsYield
With potassium carbonate In N,N-dimethyl-formamide at 25℃; for 24h;70%

ethyl aminocrotonate

105-45-3

acetoacetic acid methyl ester

6334-18-5

2,3-dichlorobenzylaldehyde

A

72509-76-3

ethyl methyl 1,4-dihydro-2,6-dimethyl-4(2,3-dichlorophenyl)-3,5-pyridinedicarboxylate

B

91189-59-2

4-(-2,3-dichlorophenyl)-1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylic acid methyl ester

C

79925-38-5

4-(2,3-dichloro-phenyl)-2,6-dimethyl-1,4-dihydro-pyridine-3,5-dicarboxylic acid diethyl ester

Conditions
ConditionsYield
Stage #1: acetoacetic acid methyl ester; 2,3-dichlorobenzylaldehyde; piperidine; 2-Picolinic acid In isopropyl alcohol at 40 - 45℃; for 6h;
Stage #2: ethyl aminocrotonate In isopropyl alcohol for 4h; Heating / reflux;
A 66%
B n/a
C n/a

dimethyl dihydropyridine

diethyl dihydropyridine

626-34-6

ethyl 3-aminobut-2-enoate

6334-18-5

2,3-dichlorobenzylaldehyde

72509-76-3

ethyl methyl 1,4-dihydro-2,6-dimethyl-4(2,3-dichlorophenyl)-3,5-pyridinedicarboxylate

Conditions
ConditionsYield
In hexane; isopropyl alcohol62%
94739-24-9

ethyl 2-(2,3-dichlorobenzylidene)-3-oxobutanoate

72509-76-3

ethyl methyl 1,4-dihydro-2,6-dimethyl-4(2,3-dichlorophenyl)-3,5-pyridinedicarboxylate

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: 71 percent / 2-methyl-propan-2-ol / 96 h / 25 °C
2: 72.7 percent / DBU / methanol / 48 h / 25 °C
3: 70 percent / K2CO3 / dimethylformamide / 24 h / 25 °C
View Scheme
175688-78-5

4-(2,3-Dichloro-phenyl)-2,6-dimethyl-1,4-dihydro-pyridine-3,5-dicarboxylic acid 3-(2-cyano-ethyl) ester 5-ethyl ester

72509-76-3

ethyl methyl 1,4-dihydro-2,6-dimethyl-4(2,3-dichlorophenyl)-3,5-pyridinedicarboxylate

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 72.7 percent / DBU / methanol / 48 h / 25 °C
2: 70 percent / K2CO3 / dimethylformamide / 24 h / 25 °C
View Scheme
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Chemistry

Molecular Structure:
Molecular Formula: C18H19Cl2NO4
Molecular Weight: 384.2538
IUPAC Name: 3-O-Ethyl 5-O-methyl 4-(2,3-dichlorophenyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate
Synonyms of Felodipine (CAS NO.72509-76-3): (+-)-Ethyl methyl 4-(2,3-dichlorophenyl)-1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylate ; AGON SR ; Agon ; BRN 4331472 ; Feloday ; Felodipina ; Felodipina [INN-Spanish] ; Felodipinum ; Felodipinum [INN-Latin] ; Felodur ER ; Felogard ; Flodil ; H 154/82 ; Hydac ; Modip ; Munobal ; Munobal Retard ; Plendil Depottab ; Plendil ER ; Plendil Retard ; Preslow ; Prevex ; Renedil ; Splendil ; UNII-OL961R6O2C ; dl-Felodipine ; 3,5-Pyridinedicarboxylic acid, 1,4-dihydro-4-(2,3-dichlorophenyl)-2,6-dimethyl-, ethyl methyl ester ; 3,5-Pyridinedicarboxylic acid, 4-(2,3-dichlorophenyl)-1,4-dihydro-2,6-dimethyl-, ethyl methyl ester, (+-)-
CAS NO: 72509-76-3
Classification Code: Anti-arrhythmia agents ; Antihypertensive agents ; Calcium channel blockers ; Cardiovascular Agents ; Drug / Therapeutic Agent ; Human Data ; Membrane Transport Modulators ; Reproductive Effect ; Vasodilator ; Vasodilator agents
Melting point: 142-145°C
Index of Refraction: 1.549
Molar Refractivity: 95.78 cm3
Molar Volume: 300.8 cm3
Surface Tension: 42.1 dyne/cm
Density: 1.277 g/cm3
Flash Point: 239 °C
Enthalpy of Vaporization: 73.43 kJ/mol
Boiling Point: 471.5 °C at 760 mmHg
Vapour Pressure: 4.62E-09 mmHg at 25°C

Uses

 Felodipine (CAS NO.72509-76-3) is a CALCIUM channel blocker, a drug used to control hypertension, or with other antihypertensives, chronic angina pectoris.

Toxicity Data With Reference

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
dog LDLo oral 200mg/kg (200mg/kg) LUNGS, THORAX, OR RESPIRATION: RESPIRATORY DEPRESSION

GASTROINTESTINAL: NAUSEA OR VOMITING

BLOOD: CHANGES IN SPLEEN
Yakuri to Chiryo. Pharmacology and Therapeutics. Vol. 20, Pg. 2963, 1992.
mouse LD50 intraperitoneal 76mg/kg (76mg/kg)   Iyakuhin Kenkyu. Study of Medical Supplies. Vol. 26, Pg. 239, 1995.
mouse LD50 intravenous 3100ug/kg (3.1mg/kg)   Iyakuhin Kenkyu. Study of Medical Supplies. Vol. 26, Pg. 239, 1995.
mouse LD50 oral 250mg/kg (250mg/kg)   Cardiovascular Drug Reviews. Vol. 11, Pg. 126, 1993.
mouse LD50 subcutaneous 205mg/kg (205mg/kg)   Iyakuhin Kenkyu. Study of Medical Supplies. Vol. 26, Pg. 239, 1995.
rat LD50 intraperitoneal 23mg/kg (23mg/kg)   Iyakuhin Kenkyu. Study of Medical Supplies. Vol. 26, Pg. 239, 1995.
rat LD50 intravenous 5400ug/kg (5.4mg/kg)   Iyakuhin Kenkyu. Study of Medical Supplies. Vol. 26, Pg. 239, 1995.
rat LD50 oral 1050mg/kg (1050mg/kg)   Iyakuhin Kenkyu. Study of Medical Supplies. Vol. 26, Pg. 239, 1995.
rat LD50 subcutaneous > 600mg/kg (600mg/kg)   Iyakuhin Kenkyu. Study of Medical Supplies. Vol. 26, Pg. 239, 1995.

Safety Profile

Hazard Codes of of Felodipine (CAS NO.72509-76-3): HarmfulXn
Risk Statements: 22
R22: Harmful if swallowed.
Safety Statements: 36
S36: Wear suitable protective clothing.
WGK Germany: 3
RTECS: US7968700

Specification

Interactions:
Recent findings have suggested that felodipine in combination with grapefruit juice will make toxic effects. Oral administration of felodipine is first metabolized in the gastrointestinal tract and liver by the enzyme CYP3A4. Grapefruit juice contains bergamottin that is found to have an inhibiting effect over this enzyme, so as a result the bioavailability of the drug increases, raising the risk for abnormal side effects.