Substituted N-Benzylpiperidine Amides

The present invention provides novel compounds, novel compositions, methods of their use and methods of their manufacture, such compounds pharmacologically useful in the treatment of cardiac arrhythmias. More specifically, the compounds of the present invention are Class III antiarrhythmic agents which, by effectively prolonging repolarization of a cardiac cell action potential, can be used effectively to treat certain cardiac arrhythmias.

Antiarrhythmic drugs have been grouped together according to the pattern of electrophysiological effects that they produce and/or their presumed mechanisms of action. Thus, Class I antiarrhythmic agents are characterized by being sodium channel blockers, Class II antiarrhythmic agents are beta adrenergic blockers, Class III antiarrhythmic agents prolong repolarization, and Class IV antiarrhythmic agents are calcium channel blockers.

Currently, there are very few Class III antiarrhythmic agents available for therapeutic use. Among them is bretylium. Bretylium's usefulness is limited, however, and currently its theraputic use is reserved for life-threatening ventricular arrhythmias that are refractory to other therapy. Thus, bretylium's use is generally confined to intensive care units. It is an object of this invention to provide Class III antiarrhythmic agents of broader theraputic use than existing Class III antiarrhythmic agents.

The invention relates to novel compounds of the general formula I: ##STR1## the pharmaceutically acceptable non toxic salts thereof and the hydrated forms thereof,

wherein R.sup.1 is alkyl, alkenyl or alkynyl of from one to ten carbon atoms; substituted or unsubstituted aralkyl, aralkenyl or aralkynyl of from one to ten carbon atoms and wherein said aryl substituent is one or more of alkoxy, nitro, halogen or alkylsulfonamide at any position with alkoxy or alkylsulfonamide having alkyl, alkenyl or alkynyl of one to ten carbon atoms; alkyl, alkenyl or alkynyl of from one to ten carbon atoms substituted by furanyl, imidazolyl, pyridinyl, or imidazolyl substituted by alkoxycarbonyl having alkyl, alkenyl or alkynyl of one to ten carbon atoms; arylamino; substituted aryl, unsubstituted aryl or either of them fused to substituted or unsubstituted cycloalkyl of from three to eight carbon atoms wherein said cycloalkyl substituent can be halogen; unsubstituted cycloalkyl of from three to eight carbon atoms arylcyloalkyl wherein cycloalkyl is from three to eight carbon atoms; pyridinyl; furanyl; halogen substituted furanyl; substituted or unsubstituted benzofuranyl wherein said benzofuranyl substituent can be one or more at any position of halogen, amino, nitro or alkoxy having alkyl, alkenyl or alkynyl of from one to ten carbon atoms; substituted or unsubstituted benzopyranyl wherein said substituent can be keto; thiophene; benzothiophene; or substituted or unsubstituted indene or isoindene wherein said substituent is alkyl of one to ten carbon atoms;

n is an integer of from one to ten;

R.sup.2 is unsubstituted or is alkyl, alkenyl or alkynyl of from one to ten carbon atoms or oxygen that is present as an N-oxide; R.sup.3 is hydrogen, carboxyalkyl, carboxy alkenyl or carboxy alkynyl of from one to ten carbon atoms or alkoxycarbonylalkyl, alkoxycarbonylalkenyl or alkoxycarbonylalkynyl and wherein the alkoxy moiety can have alkyl, alkenyl or alkynyl of from one to ten carbon atoms; ##STR2## is hydrogen; pyridinyl; cycloalkyl of three to eight carbon atoms or hydroxy substituted cycloalkyl of three to eight carbon atoms; furanyl; or unsubstituted or substituted phenyl wherein said phenyl substituent is one or more of alkyl or halogen substituted alkyl of one to ten carbon atoms, alkoxy from one to ten carbon atoms, nitro, amine, mono or di alkylamine, acetyl amine, acetylamide, halogen or alkoxy itself substituted by halogen substituted phenyl; and R.sup.4 is alkoxycarbonyl of from one to ten carbon atoms.

The compounds and pharmaceutical compositions thereof are useful in the antiarrhythmic methods of the invention. The invention further provides dosage unit forms adapted for oral, topical and parenteral administration. Also provided for in this invention are the pharmaceutically acceptable salts of the compounds.

As used herein, the term "alkyl" shall mean straight or branched chain carbon-carbon linkages of from one to ten carbon atoms. "Alkenyl" shall have the same meaning, except that one or more double bonds may be present therein. "Alkynyl" shall have the same meaning, except that one or more triple bonds may be present therein.

"Alkoxy" shall include alkyl, alkenyl and alkynyl, as defined above, substituted by an epoxide oxygen.

"Aralkyl" shall include alkyl, alkenyl and alkynyl, as defined above, substituted by an aryl group, which is defined below.

"Aryl" shall mean phenyl.

"Halogen" shall include fluorine, chlorine, bromine or iodine.

The term "cardiac arrhythmia" is defined to mean any variation from the normal rhythm of the heartbeat, including, without limitation, sinus arrhythmia, premature heartbeat, heartblock, fibrillation, flutter, pulsus alternans, tachycardia, paroxysmal tachycardia and premature ventricular contractions.

The term "repolarization of cardiac cells" is defined as those phases of a cardiac action potential during which time a depolarized cardiac cell is reverting to normal pre-polarization transmembrane voltage.

The term "pharmaceutically acceptable salts" refers to non-toxic salts of the compounds of this invention which are generally prepared by reacting the free base with a suitable organic or inorganic acid. Representative salts include the hydrochloride, hydroiodic, hydrobromide, sulfate, bisulfate, acetate, oxalate, valerate, oleate, palmitate, stearate, laurate, borate, benzoate, lactate, phosphate, tosylate, citrate, maleate, fumarate, succinate, tartrate, napsylate, clavulanate, methaneperoxoate and the like salts.

Compounds of the invention can be prepared readily according to the following reaction scheme or modifications thereof using readily available starting materials, reagents and conventional synthesis procedures. In these reactions, it is also possible to make use of variants which are in themselves known, but are not mentioned in greater detail. R.sup.1, R.sup.2, R.sup.3 and ##STR3## are as defined above. Y is any suitable leaving group, such as halogen, mesylate or tosylate. COZ represents a suitable acylating agent such as a carboxylic acid chloride, a carboxylic acid activated as the mixed anydride, or the carboxylic ester activated by alkylaluminum reagents. ##STR4##

Reduction of 4-acetamidopyridine Formula II affords 4-acetamido-piperidine Formula III. A method for the preparation of 4-acetamidopiperidine III involves the reduction of 4-acylamino N-benzyl pyridinium compounds by alkali metal hydrides or catalytic hydrogenation of the aromatic ring with debenzylation as described in U.K. 1,537,867 (G. O. Weston) and U.K. 1,345,872 (J. L. Archibald and J. F. Cavalla) the disclosures of which are incorporated herein by reference. Preferred reduction conditions employ a ruthenium on carbon catalyst in a solvent such as alcohol, tetra hydrofuran, (THF), or acetic acid under an atmosphere of hydrogen. Subsequent reductive alkylation of the piperidine Formula III with aldehydes Formula IV provides the N-alkylated intermediates Formula V. Preferred conditions employ Pt/C catalyst in an inert solvent such as alcohol, THF, or acetic acid under an atmosphere of hydrogen. Alternative preferred conditions employ borane-pyridine complex as the reducing agent at room temperature in alcohol, acetic acid or methylene chloride. Hydrolysis of the amide bond of acetamides Formula V provides amine intermediates Formula VI. Although hydrolysis may be effected in acid or base, the preferred method employs hydrolysis in 1.2 M HCl at 100.degree. C. Alternative preferred acylating conditions leading to amides I (R.sup.2 =lone pair) employ COZ, which can be a carboxylic acid chloride, a carboxylic acid activated as the mixed anhydride, or the carboxylic ester activated by alkylaluminum reagents.

The intermediates Formula I are subsequently converted to the quaternary salts Formula I (where R.sup.2 is not an unshared valence bond) by N-alkylating reagents R.sup.2 X Formula VIII (where X is a suitable leaving group such as halogen, mesylate, or tosylate) in an inert solvent. Preferred alkylation conditions employ acetonitrile as the solvent at room temperature.

The compounds of the present invention can be administered in such oral dosage forms as tablets, capsules, pills, powders, granules, elixers, tinctures, suspensions, syrups and emulsions. Likewise, it can also be administered in intravenous, intraperitoneal, subcutaneous or intramuscular form, all using forms known to those of ordinary skill in the pharmaceutical arts. In general, the preferred form of administration is oral. An effective but non-toxic amount of the compound is employed in the treatment of arrhythmias of the heart. The dosage regimen utilizing the compound of the present invention is selected in accordance with a variety of factors including the type, species, age, weight, sex and medical condition of the patient; with the severity of the condition to be treated; the route of administration; the renal and hepatic function of the patient; and the particular compound employed or salt thereof. An ordinarily skilled veterinarian or physician can readily determine and prescribe the effective amount of the drug required to prevent, treat or arrest the progress of the condition.

Oral dosages of the compounds of the present invention, when used for the indicated cardiac effects, will range between about 0.1 mg per kilogram of body weight per day (mg/kg/day) to about 1000 mg/kg/day and preferably 1.0 to 100 mg/kg/day. Advantageously, the compounds of the present invention can be administered in a single daily dose or the total daily dosage can be administered in divided doses of two, three or four times daily.

In the pharmaceutical compositions and methods of the present invention, the compounds described in detail below will form the active ingredient that will typically be administered in admixture with suitable pharmaceutical diluents, excipients or carriers (collectively referred to herein as "carrier" materials) suitably selected with respect to the intended form of administration, that is, oral tablets, capsules, elixers, syrups and the like, and consistent with conventional pharmaceutical practices.

For instance, for oral administration in the form of tablets or capsules, the active drug component can be combined with an oral non-toxic pharmaceutically acceptable inert carrier such as lactose, starch, sucrose, glucose, methylcellulose, magnesium stearate, dicalcium phosphate, calcium sulfate, mannitol, sorbitol and the like; for oral administration in liquid form, the active drug components can be combined with any oral non-toxic pharmaceutically acceptable inert carrier such as ethanol, glycerol, water, and the like. In the case of oral administration and in liquid form, suitable flavoring carriers can be added such as cherry syrup and the like. Moreover, when desired or necessary, suitable binders, lubricants, disintegrating agents and coloring agents can also be incorporated into the mixture. Suitable binders include starch, gelatin, natural sugars such as glucose or beta-lactose, corn sweeteners, natural and synthetic gums such as acacia, tragacanth, or sodium alginate, carboxymethylcellulose, polyethylene glycol and various waxes. Lubricants for use in these dosage forms include magnesium stearate, sodium benzoate, sodium acetate, sodium stearate, sodium chloride, sodium oleate and the like. Disintegrators include, without limitation, starch, methylcellulose, agar, bentonite, xanthan gum and the like.

The compounds of this invention can also be administered by intravenous route in doses ranging from 0.01 to 10 mg/kg/day.

Furthermore, it is also contemplated that the invention can be administered in an intranasal form topically via the use of suitable intranasal vehicles, or via transdermal routes, using those forms of transdermal skin patches well known to those of ordinary skill in that art. In the case of transdermal skin patch administration, daily dosage is continuous via the transdermal delivery system rather than divided, as in an oral delivery system.

The compounds of this invention exhibit antiarrythmic activity useful in the treatment of various cardiac arrhythmias. The test procedures employed to measure this activity of the compounds of the present invention are described below.

Guinea pigs, of either sex weighing between 200-350 g, are acutely sacrificed and the right ventricular papillary muscle is isolated. A sample of a given test compound is added using an in vitro tissue bath. Concentrations used are generally 3.times.10.sup.-5 M, but may also be as low as 3.times.10.sup.-7 M. Changes in refractory period are measured before and after adding 1 concentration (usually 3.times.10.sup.-5 M, as noted above) of a test compound to the bath. One hour is allowed for drug equilibration. A compound is considered active (Class III) if an increase in ventricular refractory period is 25 msec or more (at 3.times.10.sup.-5 M).

The preferred compounds of the invention are any or all of those specifically set forth below. The compounds are not, however, to be construed as forming the only genus that is considered as the invention and any combination of such compounds may itself form a genus or sub-genus. ##STR5##

The following non-limiting examples further illustrate details for the preparation of the compounds of the present invention. Those skilled in the art will readily understand that known variations of the conditions and processes of the following preparative procedures can be used to prepare these compounds. All temperatures are degrees Celsius unless otherwise noted. Melting points were determined on a Thomas-Hoover Unimelt Capillary Apparatus and are not corrected. Unless otherwise noted, I.R. and NMR spectra were consistent with the assigned structure.

4-Aminopyridine (101.28 g) and acetic anhydride (110 g) were mixed neat and heated at 100.degree. C. for 1/2 h. The solidified reaction mixture was triturated with acetone, filtered off, and washed with ether to afford 186.48 g of II as a white solid in two crops. Anal. calcd for C.sub.9 H.sub.12 N.sub.2 O.sub.3 : C, 55.09; H, 6.16; N, 14.26. Found: C, 55.04; H, 5.96; N, 15.22.

A solution of the product of Example 2 (75 g) in 750 mL acetic acid was reduced over PtO.sub.2 catalyst at 60 psi hydrogen atmosphere at 60.degree. C. for 7 hours. The solution was filtered, concentrated and triturated with ether to afford the title compound quantitatively as a white solid which was used directly in subsequent reactions.

A mixture of 10 g amine acetate from Example 3 and 13.48 g 4-methoxy benzaldehyde was hydrogenated in 100 mL ethanol over a Pt/C catalyst at room temperature for 3 hours. The reaction mixture was filtered and concentrated to give 74.0 g of the acetate salt of the title compound as a white solid which was hydrolyzed directly as described in Example 4. (An alternative reductive amination procedure is described in Example 5). Conversion of a sample to the free base using aqueous base and ethyl acetate extraction provided a white solid after solvent evaporation and trituration with ether: mp 140.degree.-142.degree. C.; Anal. calcd for C.sub.15 H.sub.22 N.sub.2 O.sub.2 : C, 68.67; H, 8.45; N, 10.68. Found: C, 65.26; H, 8.60; N, 10.77.

A) A solution of 50 g of the product of Example 4 was dissolved in 500 mL of 1.2N HCl and heated at 100.degree. C. for 8 h. The solution was made alkaline with 50% aq. NaOH and extracted three times with ether. The combined organic layers were washed with water and saturated brine, dried over sodium sulfate, and concentrated to give the title compound as 28 g of clear oil which was used without further purification.

B) (Alternative general reductive alkylation procedure) A solution of 50 mmol amine acetate (product of Example 3) and 100 mmol of 4-methoxybenzaldehyde in 125 mL methylene chloride and 15 mL acetic acid was treated with 50 mmol of borane-pyridine complex and allowed to stir at room temperature overnight. The removal of volatiles by rotary evaporation afforded the acetamide of Example 4 as an oil which was dissolved in 300 mL of 1.2N HCl and heated overnight on a steam bath. The cooled reaction mixture was extracted once with a 50 mL portion of ethyl acetate which was discarded. The aqueous layer was made basic with aq. NaOH and extracted three times with 50 mL ether. The combined layers were washed with water and dried over sodium sulfate. Solvent removal afforded the title compound as a crude oil (yield typically 60-70% for two steps) which was used directly without further purification.

A) 10 mmol of the amine of Example 5 is dissolved in a mixture of 25 mL chloroform and 11 mmol of triethylamine cooled to 0.degree. C. A solution of 11 mmol of the acyl chloride neat or dissolved in 25 mL chloroform is added dropwise and the reaction mixture is allowed to stir for 1 h. Volatiles are removed in vacuo and the residue is partitioned between dilute aqueous base and ethyl acetate. Drying of the ethyl acetate extract and evaporation leads to the crude product which is optionally purified by flash chromatography on silica gel using 92.5:7:0.5 chloroform:ethanol:ammonium hydroxide and crystallized from ethyl acetate/hexane or converted to the HCl salt using dioxane/HCl followed by recrystallization from methanol/ether.

B) A stirred solution of 10 mmol acylating acid in 25 mL chloroform is treated with 10 mmol of triethylamine followed by 10 mmol of isobutyl chloroformate. After 10 minutes at ambient temperature the amine of Example 5 was added and the reaction is allowed to stir for 1/2 h. The reaction mixture is washed with 10% NaOH solution and the organic layer is dried and evaporated to give a residue which is optionally purified by flash chromatography on silica gel using 92.5:7:0.5 chloroform:ethanol:ammonium hydroxide recrystallized from ethyl acetate converted to the HCl salt using dioxane/HCl followed by recrystallization from methanol/ether.

A solution of 200 mg of the amide of Example 6 in 5 mL acetone was treated with 4 drops of iodomethane. The reaction mixture was stirred for 18 h and the white crystalline precipitate was filtered off to afford 206 mg of white solid which was recrystallized from acetonitrile to give 128 mg of quaternary iodide as fluffy white needles, mp 236.degree.-237.degree. C.

A solution of 0.50 g of the amide of Example 6 in 10 mL CH.sub.2 Cl.sub.2 was treated with 300 mg of m-chloroperoxybenzoic acid at 0.degree. C. After 1 h the solution was washed consecutively with 10 mL 1N NaOH, water, and sat'd. brine. The solution was dried over sodium sulfate and concentrated to afford 0.51 g of white solid which was recrystallized from CH.sub.2 Cl.sub.2 /ethyl acetate to give 0.33 g of an N-oxide as a white powder, mp 200.5.degree.-202.5.degree. C.

Using the procedures of Examples 2 through 8 and making the appropriate substitutions at positions R.sub.1, R.sub.2, R.sub.3, and X, the following products were obtained as presented in Table I, below. Table I specifies the moiety at R.sub.1, R.sub.2, R.sub.3 and ##STR10## the number of methylenes represented by n, the compound's melting point range in degrees Celsius (where available) and the compound's elemental analysis. ##STR11## All piperidinyls are 4-piperidinyl unless otherwise noted. Example R.sup.1 R.sup.2 R.sup.3 X n mp, deg. C. Analysis 9 ##STR12## H ##STR13## 1 C.sub.18 H.sub.21 N.sub.3 O 10 ##STR14## H ##STR15## 1 C.sub.18 H.sub.21 N.sub.3 O 11 ##STR16## H ##STR17## 1 C.sub.18 H.sub.21 N.sub.3 O 12 ##STR18## H ##STR19## 1 C.sub.26 H.sub.33 ClN.sub.2 O.sub.2 13 ##STR20## H ##STR21## 1 155-157 C.sub.19 H.sub.28 N.sub.2 O 14 ##STR22## H ##STR23## 1 168-169.5 C.sub.19 H.sub.23 N.sub.3 O 15 ##STR24## H ##STR25## 1 155.5-158 C.sub.17 H.sub.20 N.sub.2 O.sub.2 16 ##STR26## H ##STR27## 1 170-171 C.sub.20 H.sub.30 N.sub.2 O.sub.2 17 CH.sub.3 H ##STR28## 1 137-140 C.sub.15 H.sub.22 N.sub.2 O.sub.2 18 ##STR29## H ##STR30## 1 136-137 C.sub.18 H.sub.22 N.sub.2 O.sub.3 19 ##STR31## H ##STR32## 1 142-143 C.sub.23 H.sub.28 N.sub.2 O.sub.2 20 ##STR33## H ##STR34## 1 135-137 C.sub.22 H.sub. 26 N.sub.2 O.sub.2 21 ##STR35## H ##STR36## 1 136-138 C.sub.22 H.sub.24 N.sub.2 O.sub.3 22 ##STR37## H ##STR38## 1 C.sub.19 H.sub.23 N.sub.3 O.sub.2 23 ##STR39## H ##STR40## 1 161-162 C.sub.18 H.sub.22 N.sub.2 O.sub.2 S 24 ##STR41## H ##STR42## 1 200-202 C.sub.23 H.sub.24 N.sub.2 O.sub.4 25 ##STR43## H ##STR44## 1 210-211 C.sub.19 H.sub.24 N.sub.2 O.sub.2 26 ##STR45## H ##STR46## 1 134-137 C.sub.24 H.sub.32 N.sub.2 O.sub.4 27 CH.sub.3 H ##STR47## 2 162-164 C.sub.16 H.sub.24 N.sub.2 O.sub.2 28 ##STR48## H ##STR49## 1 178.5-179.5 C.sub.18 H.sub.22 N.sub.2 O.sub.2 29 ##STR50## H ##STR51## 1 140-141 C.sub.22 H.sub.24 N.sub.2 O.sub.3 30 ##STR52## H ##STR53## 1 135-137 C.sub.23 H.sub.28 N.sub. 2 O.sub.2 31 ##STR54## H ##STR55## 1 156-158 C.sub.24 H.sub.30 N.sub.2 O.sub.2 32 ##STR56## H ##STR57## 1 122-124 C.sub.20 H.sub.26 N.sub.2 O.sub.3 33 ##STR58## H ##STR59## 1 132-134 C.sub.24 H.sub.28 N.sub.2 O.sub.3 34 ##STR60## H ##STR61## 1 148-149 C.sub.22 H.sub.23 ClN.sub.2 O.sub.3 35 ##STR62## H ##STR63## 1 156-158 C.sub.23 H.sub. 26 N.sub.2 O.sub.2 36 ##STR64## H ##STR65## 1 140-142 C.sub.23 H.sub.26 N.sub.2 O.sub.4.HCl 37 ##STR66## H ##STR67## 1 147-148 C.sub.24 H.sub.28 N.sub.2 O.sub.5 38 ##STR68## H ##STR69## 1 126-128 C.sub.22 H.sub.23 ClN.sub.2 O.sub.3 39 ##STR70## H ##STR71## 1 158-160 C.sub.22 H.sub.24 N.sub.2 O.sub.2 S 40 ##STR72## H ##STR73## 1 270-272 C.sub.23 H.sub.24 N.sub.2 O.sub.4.HCl 41 ##STR74## H ##STR75## 1 oil C.sub.22 H.sub.25 N.sub.2 O.sub.2.HCl 42 ##STR76## H ##STR77## 1 146-148 C.sub.23 H.sub.28 N.sub.2 O.sub.3 43 ##STR78## H ##STR79## 1 147-149 C.sub.23 H.sub.28 N.sub.2 O.sub.3 44 ##STR80## H ##STR81## 1 145-147 C.sub.20 H.sub.25 N.sub.3 O.sub.2 45 ##STR82## H ##STR83## 1 150-152 C.sub.21 H.sub.25 N.sub.3 O.sub.2 46 ##STR84## H ##STR85## 1 142-144 C.sub.23 H.sub.26 N.sub.2 O.sub.3 47 ##STR86## H ##STR87## 1 131-133 C.sub.22 H.sub.28 N.sub.2 O.sub.2 48 ##STR88## H ##STR89## 1 141-143 C.sub.23 H.sub.28 N.sub.2 O.sub.2 49 ##STR90## H ##STR91## 1 125-127 C.sub.23 H.sub.30 N.sub.2 O.sub.2.HCl 50 ##STR92## H ##STR93## 1 92-96 C.sub.23 H.sub.28 N.sub.2 O.sub.2.HCl 51 ##STR94## H ##STR95## 1 134.5-135 C.sub.22 H.sub.26 N.sub.2 O.sub.3 52 ##STR96## H ##STR97## 1 C.sub.21 H.sub.26 N.sub.2 O.sub.2 53 ##STR98## H ##STR99## 1 190-192 C.sub.22 H.sub.23 N.sub.3 O.sub.5 54 ##STR100## H ##STR101## 1 197-199 C.sub.22 H.sub.25 N.sub.3 O.sub.4 55 ##STR102## H ##STR103## 1 C.sub.17 H.sub.24 N.sub. 2 O.sub.2 56 ##STR104## H ##STR105## 1 210-212 C.sub.22 H.sub.24 Cl.sub.2 N.sub.2 O.sub.2 57 ##STR106## H ##STR107## 1 142-143 C.sub.24 H.sub.30 N.sub.2 O.sub.2 58 ##STR108## H ##STR109## 1 133-135 C.sub.18 H.sub.21 BrN.sub.2 O.sub.3 59 ##STR110## H ##STR111## 1 155-157 C.sub.21 H.sub.22 N.sub.2 O.sub.3 60 ##STR112## H ##STR113## 1 215-218 C.sub.23 H.sub.29 N.sub.3 O.sub.4 S 61 CH.sub.3 H ##STR114## 1 143-144 C.sub.14 H.sub.19 N.sub.3 O.sub.3 62 ##STR115## H ##STR116## 1 155-157 C.sub.21 H.sub.21 N.sub.3 O.sub.4 63 CH.sub.3 H ##STR117## 1 162-164 C.sub.14 H.sub.19 ClN.sub.2 O 64 ##STR118## H ##STR119## 1 137-139 C.sub.21 H.sub.21 ClN.sub.2 O.sub.2 65 ##STR120## H ##STR121## 1 157-159 C.sub.24 H.sub.30 N.sub.2 O.sub.2 66 ##STR122## CH.sub.3 H ##STR123## 1 236-237 C.sub.23 H.sub.26 N.sub. 2 O.sub.3.Hl 67 ##STR124## H ##STR125## 1 184-185.5 C.sub.21 H.sub.28 N.sub.2 O.sub.2 68 CH.sub.3 H ##STR126## 1 163-164.5 C.sub.13 H.sub.19 N.sub.3 O 69 CH.sub.3 H ##STR127## 1 103-105 C.sub.15 H.sub.22 N.sub.2 O.sub.2 70 ##STR128## H ##STR129## 1 114-115 C.sub.22 H.sub.24 N.sub.2 O.sub.3 71 CH.sub.3 H ##STR130## 1 C.sub.15 H.sub.22 N.sub.2 O.sub.2 72 ##STR131## O H ##STR132## 1 200.5-202.5 C.sub.22 H.sub.24 N.sub.2 O.sub.4 73 ##STR133## H H 1 C.sub.15 H.sub.18 N.sub.2 O.sub.2 74 CH.sub.3 H ##STR134## 1 145-147 C.sub.16 H.sub.23 N.sub.3 O.sub.2.CHOOOH 75 ##STR135## H ##STR136## 1 230-232 C.sub.23 H.sub.25 N.sub.3 O.sub.3 76 ##STR137## H ##STR138## 1 C.sub.22 H.sub.25 ClN.sub.2 O.sub.3 77 ##STR139## H ##STR140## 1 C.sub.23 H.sub.26 N.sub.2 O.sub.4 78 ##STR141## H ##STR142## 1 C.sub.23 H.sub.27 N.sub.3 O.sub.2.2(HCl) 79 ##STR143## H ##STR144## 1 189-190 C.sub.22 H.sub.23 N.sub.3 O.sub.5 80 ##STR145## H ##STR146## 1 98-100 C.sub.22 H.sub.27 N.sub.3 O.sub.3.2(HCl) 81 CH.sub.3 H ##STR147## 1(substituted byCO.sub.2 CH.sub.2 CH.sub.3) C.sub.17 H.sub.24 N.sub.2 O.sub.3 82 ##STR148## CH.sub.2 CO.sub.2 CH.sub.2 CH.sub.3 ##STR149## 1 C.sub.26 H.sub.31 ClN.sub.2 O.sub.5 83 ##STR150## CH.sub.2 CO.sub.2 H ##STR151## 1 C.sub.24 H.sub.26 N.sub.2 O.sub.5 84 ##STR152## H ##STR153## 1 152-153 C.sub.24 H.sub.30 N.sub.2 O.sub.2 85 ##STR154## H ##STR155## 1 198-200 C.sub.21 H.sub.22 N.sub.2 O.sub.3 86 CH.sub.3 H ##STR156## 1 C.sub.12 H.sub.18 N.sub.2 O.sub.2 87 ##STR157## H ##STR158## 1 C.sub.23 H.sub.28 N.sub.2 O.sub.2 88 ##STR159## H ##STR160## 1 C.sub.20 H.sub.22 N.sub. 2 OF.sub.3 89 ##STR161## H ##STR162## 1 C.sub.21 H.sub.27 N.sub.2 O.sub.3

While the invention has been described and illustrated with reference to certain preparative embodiments thereof, those skilled in the art will appreciate that various changes, modifications and substitutions can be made therein without departing from the spirit and scope of the invention. For example, effective dosages other than the preferred range as set forth herein above may be applicable as a consequence of variations in the responsiveness of the mammal being treated for severity of cardiac arrhythmia, dosage-related adverse effects, if any, and analogous considerations. Likewise, the specific pharmacological responses observed may vary according to and depending upon the particular active compounds selected or whether there are present certain pharmaceutical carriers, as well as the type of formulation and mode of administration employed, and such expected variations for differences in the results are contemplated in accordance with the objects and practices of the present invention. It is intended, therefore, that the invention be limited only by the scope of the claims which follow, and that such claims be interpreted as broadly as is reasonable.