51-06-9 Usage
Description
Procainamide and its analogs were employed by Dr Claude
Beck in a series of cardiac surgeries during the early 1930s. The
compound was used to alleviate arrhythmias that present
during the procedures, and was selected for its favorable tissue
absorption properties. Procainamide’s central amide provides
it protection from inactivating esterase action and allows oral
administration of the compound. Procainamide was approved
for use in the United States in 1950.
Uses
Different sources of media describe the Uses of 51-06-9 differently. You can refer to the following data:
1. Procainamide is used in the management of atrial and
ventricular tachydysrhythmias.
2. Procainamide is intended for treating paroxysmal atrial tachycardia, atrial fibrillation, premature ventricular contraction, and ventricular tachycardia. For quickly reaching therapeutic concentrations, parenternal introduction of procainamide is preferred over cynidine.
Definition
ChEBI: 4-Aminobenzamide substituted on the amide N by a 2-(diethylamino)ethyl group. It is a pharmaceutical antiarrhythmic agent used for the medical treatment of cardiac arrhythmias.
Biological Functions
Procainamide (Pronestyl, Procan SR) is a derivative of
the local anesthetic agent procaine. Procainamide has a
longer half-life, does not cause CNS toxicity at therapeutic
plasma concentrations, and is effective orally.
Procainamide is a particularly useful antiarrhythmic
drug, effective in the treatment of supraventricular, ventricular,
and digitalis-induced arrhythmias.
Synthesis Reference(s)
Synthesis, p. 714, 1975 DOI: 10.1055/s-1975-23900
Mechanism of action
The chemical difference between procainamide and procaine lies in the replacement of the ester group with an amide group. The action of procainamide is qualitatively similar to the action of procaine. Its effect on the heart is identical to that of quinidine. As an antiarrhythmic, procainamide is preferred over procaine because unlike procaine, it is better absorbed when taken orally and it is more difficult for the esterases of the plasma to hydrolyze it, which results in long-lasting action.
Clinical Use
Procainamide is an effective antiarrhythmic agent when
given in sufficient doses at relatively short (3–4 hours)
dosage intervals. Procainamide is useful in the treatment
of premature atrial contractions, paroxysmal atrial tachycardia,
and atrial fibrillation of recent onset. Procainamide
is only moderately effective in converting atrial flutter or
chronic atrial fibrillation to sinus rhythm, although it has value in preventing recurrences of these arrhythmias
once they have been terminated by direct current (DC)
cardioversion.
Procainamide can decrease the occurrence of all
types of active ventricular dysrhythmias in patients with
acute myocardial infarction who are free from A-V dissociation,
serious ventricular failure, and cardiogenic
shock. About 90% of patients with ventricular premature
contractions and 80% of patients with ventricular
tachycardia respond to procainamide administration.
Although the spectrum of action and electrophysiological
effects of quinidine and procainamide are similar,
the relatively short duration of action of procainamide
has tended to restrict its use to patients who
are intolerant of or unresponsive to quinidine.
Side effects
Acute cardiovascular reactions to procainamide administration
include hypotension, A-V block, intraventricular
block, ventricular tachyarrhythmias, and complete
heart block. The drug dosage must be reduced or even
stopped if severe depression of conduction (severe prolongation
of the QRS interval) or repolarization (severe
prolongation of the QT interval) occurs.
Long-term drug use leads to increased antinuclear
antibody titers in more than 80% of patients; more than
30% of patients receiving long-term procainamide therapy
develop a clinical lupus erythematosus–like syndrome.
The symptoms may disappear within a few days
of cessation of procainamide therapy, although the tests
for antinuclear factor and lupus erythematosus cells
may remain positive for several months.
Procainamide, unlike procaine, has little potential to
produce CNS toxicity. Rarely, patients may be confused
or have hallucinations.
Synthesis
Procainamide, 4-amino-N-[2-(diethylamino)ethyl]benzamide (18.1.3), is
synthesized by reacting 4-nitrobenzoic acid chloride with N,N-diethylethylendiamine and
subsequent reduction of the nitro group of the resulting 4-nitro-N-[2-(diethylamino)ethyl]benzamide
(18.1.2) into an amino group.
Drug interactions
The inherent anticholinergic properties of procainamide
may interfere with the therapeutic effect of cholinergic
agents. Patients receiving cimetidine and procainamide
may exhibit signs of procainamide toxicity, as cimetidine
inhibits the metabolism of procainamide. Simultaneous use of alcohol will increase the hepatic clearance of procainamide.
Procainamide may enhance or prolong the
neuromuscular blocking activity of the aminoglycosides
with the potential of producing respiratory depression.
The simultaneous administration of quinidine or amiodarone
may increase the plasma concentration of procainamide.
Metabolism
Metabolites of
procainamide include p-aminobenzoic acid and N-acetylprocainamide. Interestingly, the acetylated
metabolite is also active as an antiarrhythmic. Its formation accounts for up to one-third of the
administered dose and is catalyzed by the liver enzyme N-acetyl transferase. Because acetylation is
strongly influenced by an individual's genetic background, marked variability in the amounts of this
active metabolite may be observed from patient to patient. Renal excretion dominates, with
approximately 90% of a dose excreted as unchanged drug and metabolites. The elimination half-life
is approximately 3.5 hours. A substantial percentage (60–70%) of patients on procainamide show
elevated levels of antinuclear antibodies after a few months. Of these patients, between 20 and 30%
develop a drug-induced lupus syndrome if therapy is continued. These adverse effects, which are
attributed to
the aromatic amino group, are observed more frequently and more rapidly in “slow acetylators.”
Usually, the symptoms associated with procainamide-induced lupus syndrome subside fairly rapidly
after the drug is discontinued. These problems, however, have discouraged long-term procainamide
therapy.
Toxicity evaluation
Procainamide is a class 1a antiarrhythmic that has a mechanism
that resembles quinidine by binding to the transmembrane
Nat channels and decreasing the number available
for depolarization. This creates a delay of Nat entry into the
cardiac myocyte during phase 0 of depolarization. As a result,
the upslope of depolarization is slowed and the QRS complex
widens. Procainamide may also affect phase 3 of the action
potential, resulting in prolongation of repolarization and
manifesting as QTc prolongation on the electrocardiogram
(EKG). Unlike quinine, however, procainamide lacks alphablocking
activity and quinidine’s vagolytic ability.
Vasodilation associated with procainamide toxicity
(>10 mg ml°1) is due to interference with ganglionic transmission
of catecholamine neurotransmitters and/or central
nervous system (CNS) sympathetic inhibition. A reflex tachycardia
may occur in response to this vasodilation. Rapid
intravenous dosing of procainamide can be dangerous as its
initial Vd is less than its final; thus adverse myocardial effects
can often be seen as the initial ‘compartment’ and includes the
cardiovascular system. Myocardial complications can initially
be more pronounced. Procainamide may also have weak
anticholinergic effects that produce tachycardia. Negative
inotropic effects may occur in toxicity. The NAPA metabolite of
procainamide lacks Nat channel blocking activity but still
retains blockade of the Kt rectifier currents. It is therefore
pharmacologic, similar to a type III antidysrhythmic.
Precautions
Contraindications to procainamide are similar to those
for quinidine. Because of its effects on A-V nodal and
His-Purkinje conduction, procainamide should be administered
with caution to patients with second-degree
A-V block and bundle branch block. Procainamide
should not be administered to patients who have shown
procaine or procainamide hypersensitivity and should
be used with caution in patients with bronchial asthma.
Prolonged administration should be accompanied by
hematological studies, since agranulocytosis may occur.
Check Digit Verification of cas no
The CAS Registry Mumber 51-06-9 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 5 and 1 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 51-06:
(4*5)+(3*1)+(2*0)+(1*6)=29
29 % 10 = 9
So 51-06-9 is a valid CAS Registry Number.
InChI:InChI=1/C13H21N3O/c1-3-16(4-2)10-9-15-13(17)11-5-7-12(14)8-6-11/h5-8H,3-4,9-10,14H2,1-2H3,(H,15,17)
51-06-9Relevant articles and documents
Mechanochemical catalytic transfer hydrogenation of aromatic nitro derivatives
Portada, Tomislav,Margeti?, Davor,?trukil, Vjekoslav
supporting information, (2018/12/11)
Mechanochemical ball milling catalytic transfer hydrogenation (CTH) of aromatic nitro compounds using readily available and cheap ammonium formate as the hydrogen source is demonstrated as a simple, facile and clean approach for the synthesis of substituted anilines and selected pharmaceutically relevant compounds. The scope of mechanochemical CTH is broad, as the reduction conditions tolerate various functionalities, for example nitro, amino, hydroxy, carbonyl, amide, urea, amino acid and heterocyclic. The presented methodology was also successfully integrated with other types of chemical reactions previously carried out mechanochemically, such as amide bond formation by coupling amines with acyl chlorides or anhydrides and click-type coupling reactions between amines and iso(thio)cyanates. In this way, we showed that active pharmaceutical ingredients Procainamide and Paracetamol could be synthesized from the respective nitro-precursors on milligram and gram scale in excellent isolated yields.
ORGANIC REACTIONS CARRIED OUT IN AQUEOUS SOLUTION IN THE PRESENCE OF A HYDROXYALKYL(ALKYL)CELLULOSE OR AN ALKYLCELLULOSE
-
Page/Page column 251; 252, (2017/08/21)
The present invention relates to a method of carrying out an organic reaction in aqueous solution in the presence of a hydroxyalkyl(alkyl)cellulose or an alkylcellulose.
Sulphuric acid immobilized on silica gel (H2SO4-SiO2) as an eco-friendly catalyst for transamidation
Rasheed,Rao, D. Nageswar,Reddy, A. Siva,Shankar, Ravi,Das, Parthasarathi
, p. 10567 - 10574 (2015/02/05)
A novel method of transamidation of carboxamides with amines by using catalytic amounts of H2SO4-SiO2 has been developed under solvent free conditions. The transamidation is compatible with a wide range of aromatic, heteroaromatic, aliphatic, cyclic/acyclic primary or secondary amines. The metal/solvent-free conditions represent a significant improvement over other existing methods as the reaction can be performed in open air conditions and no column purification is required. The versatility of this methodology was further demonstrated by synthesizing the commercially available drug procainamide.
