DIARYL PIPERAZINOACETAMIDE COMPOUNDS AS ANTIMUSCARINIC AGENTS

The present invention is directed to novel diaryl piperazinoacetamide compounds useful as antimuscarinic agents. Typically, these compounds can be used in the treatment of Parkinson's disease, motion sickness and for the inhibition of gastric acid secretion.

GENERAL BACKGROUND Other diaryl piperazinoacetamide compounds have been disclosed in the literature such as Chemical Abstract 113(7)59226h, 111(5)39321, and 81(5)25292g; and J^ Heterocvclic Chem. 20:1335-1338 (1983) and 20:1339-1349 (1983). None of the foregoing describe the novel compounds of the present invention.

BACKGROUND OF THE PRESENT INVENTION Muscarinic receptors are one of two general types of cholinergic receptors and are distributed in the central nervous system and the peripheral organs. Inhibition of the effects of muscarinic agents at these receptors can produce the interruption of parasympathetic and sympathetic cholinergic nerve stimulation, e.g., decreased gastrointestinal motility, decreased gastric secretion, dry mouth, drying of the mucous membranes in general, mydriasis, loss of accommodation, urinary retention, decreased sweating and compensatory cutaneous flush.

bronchial and biliary dilation, tachycardia and several central nervous system effects. Since some of these effects are desirable under certain circumstances, antimuscarinic agents, also known as muscarinic antagonists, have been developed in order to treat a wide variety of clinical conditions in the gastrointestinal tract, respiratory tract, cardiovascular system, central nervous system, genito-urinary tract, in ophthalmology and in conjunction with anesthesia. Goodman and Gilman's The PharmacologicalBasisofTherapeutics, 8th ed. Pergamon Press 1990, incorporated herein by reference.

For example, antimuscarinics have been used in the treatment of the following conditions: to dilate the pupil in order to facilitate visualization of the optic fundus and to paralyze accommodation; to break adhesion between the iris and lens; to treat acute iritis, uveitis, irdiocylitis and keratitis; to treat malignant glaucoma; preanesthesia medication to decrease excessive secretions; to treat sialorrhea, acute coryza, hay fever and rhinitis; to treat bronchial asthma; suppress vagally mediated bradyarrhythmias, heart block or cardiac syncope; to relieve urinary frequency and urgency; to control enuresis; to relieve ureteral colic; to treat functional gastrointestinal disorders; to treat motion sickness; to suppress gastric secretions; and to treat Parkinson's disease.

Until the discovery of pirenzepine and subsequent molecular cloning, it was not known that muscarinic receptors consisted of five subtypes designated as Mi through M ₅ . All five subtypes of muscarinic receptors are found in the central nervous system. The other tissues in which muscarinic receptors have been found are the heart, smooth muscle, secretory glands and autonomic ganglia.

Pirenzepine, a selective Mi antimuscarinic compound, was shown to selectively inhibit gastric acid secretion at concentrations which did not affect several other responses to muscarinic agonisti , Therefore, by improving the selectivity of antimuscarinic compounds to muscarinic subtype receptors it may be possible to diminish undesirable responses and/or enhance the selectivity of the desired response.

It is an object of the present invention to provide novel compounds useful as therapeutic antimuscarinic agents. Additionally, the present invention provides antimuscarinic compounds which exhibit activity, and in some cases selectivity, for the Mi receptor. Thera¬ peutically these compounds may be used for a wide variety of conditions and in particular for the treatment of Parkinson's disease, motion sickness, and the inhibition of gastric acid secretion.

SUMMARY OF THE PRESENT INVENTION A compound of formula:

and the pharmaceutically acceptable salts thereof, wherein each of X and X' are independently -H,-Cι~ ₄ alkyl,

-Cl, -Br, -I, -F, -(CH ₂ ) _m CN, -(CH ₂ ) _m COORι, -(CH ₂ ) _m CONR ₂ R ₃ , CF ₃ , -(CH ₂ ) _m NHQ, -(CH ₂ ) _m O(CH ₂ )p'Z,

-CH ₂ -NR ₂ R ₃ , -NH ₂ , -SO ₃ H, S0 ₂ NR ₂ R ₃ ,

each of Y and Y' are independently -C- or -N-; m is 0 or 1; p is 1, 2, 3, or 4; p' is 0, 1, 2, 3, or 4;

R and Ri are each independently H or C ₁ -C ₄ alkyl; each of R ₂ and R ₃ are independently H, -CH _3f -CH ₂ CH ₃ , C ₄ -C ₇ cycloalkyl or taken together with the nitrogen atom form a heterocyclic ring having from 4 to 6 carbon atoms;

R ₄ is C ₁ -C ₄ alkyl;

Z is H, OH, -NR ₂ R ₃ , -C(0)ORι, -C(0)CH ₂ N N-R;

or -OC(0)CH ₂ -N N-R; and

Q is -C(0)R _f -(CH ₂ )p.C(0)ORi, -C(O) (CH ₂ ) _p C(0)ORι, -C(0)CH=CHC(0)ORι or -S0 ₂ - y in which the phenyl moiety is

optionally substituted with methyl, methoxy, CF ₃ or N0 ₂ , provided that when Y or Y' are -N-, Y and Y' are unsubstituted, provided that when Y is -N-, X is an ortho -NH ₂ or H, provided that when Y' is -N-, X' is an ortho -NH ₂ or H,

provided that when Z is OH, -NR ₂ R ₃ or -OC(0)CH ₂ N N-R,

\_ p' is 2, 3, or 4, and provided that when R is H, then X or X' are not H, methyl, Cl, Br, I or F.

The compounds of the present invention may be used to treat conditions responsive to antagonism of muscarinic receptors, and, more preferably, muscarinic receptors of the Mi receptor subtype. Some conditions responsive to treatment with the compounds of Formula I are motion sickness, Parkinson's disease and conditions responsive to inhibition of gastric acid secretion such as peptic ulcer disease.

PREFERRED EMBODIMENTS OF THE PRESENT INVENTION Formula I of the present invention is a N- disubstituted piperazino moiety. One nitrogen of the piperazino moiety is substituted (designated as R) with either hydrogen or a Cι_ ₄ alkyl. Preferably, R is Cι_ ₄ alkyl, and, more preferably, methyl. The other nitrogen of the piperazino moiety is substituted with an acetamido moiety on which the nitrogen is disubstituted; the disubstitution on the nitrogen does not have to be identical.

The diaryl structures attached directly to the nitrogen atom of the acetamido moiety can each be phenylene (Y or Y' are C) or a pyridine moiety (Y or Y' are N) . When Y or Y' are N, then the N remains unsubstitued, i.e., when there is a pyridine moiety, the attachment to the remainder of the molecule is not via the nitrogen atom of the pyridine moiety nor is the nitrogen atom substituted with X or X'. Additionally, when ϊ or ϊ ¹ are N, respectively X or X' are substituents ortho to N and are limited to hydrogen

or amino substituents. It is intended that this ortho sustitution does not include substitution at the point of attachment of the ring structures to the rest of the molecule. Y or Y' can be the same or different. Preferably, Y and Y' are the same, and more preferably, Y and Y' are each C.

X or X' can be the same or different and represent substitutents at the same or different positions on the ring structures with the foregoing caveat in the case where Y and/or Y' are N (a nitrogen atom). Preferably, X and X' are different.

It is intended that the generic structure of Formula I represents that X and/or X' are not at the same position on the ring structures as that position which is attached to the rest of the molecule. If the point of attachment of the ring structures to the remainder of the molecule is position 1, then each of X and/or X' independently can be 2, 3, 4, 5 or 6. Preferably, X and/or X' are at position number 4, commonly known as the para position.

Each of X and X' are independently -H,-Cι~ ₄ alkyl, -Cl, -Br, -I, -F, -(CH ₂ ) _m CN, -(CH ₂ ) _m COOR ₄ , -(CH ₂ ) _m CONR ₂ R3, CF _3f -(CH ₂ ) _m NHQ, -(CH ₂ ) _m O(CH ₂ ) _p -Z, -CH ₂ -NR ₂ R ₃ , NH ₂ , -S0 ₃ H, S0 ₂ NR ₂ R ₃ ,

Wherein p is 1, 2, 3 or 4; p' is 0,1,2,3 or 4; and m is 0 or 1.

Each of R ₂ and R ₃ are independently H, -CH ₃ , -CH ₂ CH ₃ , C4-C7 cycloalkyl or taken together form a heterocyclic ring having from 4 to 6 carbon atoms; r—v

R is C ₁ -C ₄ alkyl; Z is H, OH, -NR ₂ R ₃ ,-C(0)CH ₂ -N N-R;

-C(0)OR _I , or OC(0)CH ₂ -N N-R; and

Q is -C(0)R _4f -(CH ₂ ) _p . C(0)ORι, -C(O) (CH ₂ ) _p C(0)ORι, -C(0)CH=CHC(0)ORι or -S0 ₂ -phenyl in which the phenyl

10 moiety is optionally substituted with C1-C ₄ alkyl or alkoxy, CF ₃ or N0 ₂ .

Preferably, at least one of X or X' is -(CH ₂ ) _m NR ₂ R ₃ , hydrogen, -(CH ₂ ) _m NHQ, -(CH ₂ ) _m O(CH ₂ ) _p «Z, or C ₁ - ₄ alkyl. More

15 preferably, only one of X or X' is H. Preferably, m is 0. Each of R ₂ and R ₃ are preferably hydrogen, methyl, ethyl or together form a heterocyclic ring having 4 or 6 carbon atoms. Preferably, R4 is methyl, and/or Ri is hydrogen, methyl or tert-butyl. Preferably m is 0 and/or R ₂ and R ₃

20 are each H. When Z is other than H or -C(0)ORι, or -C(0)CH -N N-R, then p' is 2, 3 or 4.

\-J

Certain terms as used herein have the defined following _?( . meanings:

(1) "C ₁ - ₄ alkyl" means a straight or branched alkyl moiety having 1, 2, 3 or 4 carbon atoms such as methyl, ethyl, n-propyl, isopropyl, n-butyl and tert-butyl;

30

(2) "treatment" means to prevent contracting the specified disease or to relieve in part or in whole a patient's disease or the symptoms related therewith;

35

(3) "patient" means warm-blooded animals, such as for example rats, mice, dogs, cats, guinea pigs, and primates such as humans; and

(4) "optionally substituted" means that the named substituent may or may not be present in the compound of interest, and, if regarding optional substitution of a phenyl ring, if not otherwise designated, the substitution may be mono-, di-, or tri-substitution at any appropriate position on the ring, but preferably at a position other than the position which provides attachment to the remainder of the molecule.

As used herein, the term "Hal", "halo" or "halide" refers to a chlorine, fluorine, bromine or iodine atom.

The compounds of formula (I) may be prepared using techniques and procedures well known and appreciated by one of ordinary skill in the art. A general synthetic procedure for preparing these compounds is set forth in Scheme A. In Scheme A, all substituents unless otherwise indicated are as previously defined.

Scheme A

In step a, the appropriate amine of structure (1) is acetylated with an appropriate halo acetyl halide of structure (2) to give the corresponding halo acetamide of structure (3).

For example, the appropriate amine of structure (1) is contacted with 1-3 molar equivalents of the appropriate halo acetyl halide of structure (2) in the presence of an appropriate non-nucleophilic base, such as triethylamine, diethylaminopyridine or pyridine. The reactants are typically contacted in a suitable organic solvent such as acetonitrile. The reactants are typically stirred together for a period of time ranging from 10-48 hours and at a temperature range of from 0°C to reflux. The corresponding halo acetamide of structure (3) is recovered from the reaction zone by extractive methods as is known in the art.

In step b, the appropriate halo acetamide of structure (3) is reacted with the appropriate piperazine of structure (4) to give the piperazineacetamide of formula (I).

For example, the appropriate halo acetamide of structure (3) is contacted with 1-4 molar equivalents of the appropriate piperazine of structure (4). The reactants are typically contacted in a suitable organic solvent such as acetonitrile or chloroform. The reactants are typically stirred together for a period of time ranging from 10-48 hours and at a temperature range of from room temperature to reflux. The corresponding piperazineacetamide of formula (I) is recovered from the reaction zone by extractive methods as is known in the art. The piperazine¬ acetamide of formula (I) may be purified by chromatography or converted to an appropriate salt and recrystallized.

The piperazineacetamides of formula (I) wherein X or X' is -(CH ₂ )mCOORι, wherein Ri is H may be prepared from the corresponding piperazineacetamides of formula (I) wherein X or X' is -(CH ₂ )mCOORι, wherein Ri is C ₁ -C ₄ alkyl by techniques and procedures well known in the art, such as acid or base hydrolysis.

The piperazineacetamides of formula (I) wherein X or X' is -(CH ₂ )mNHQ, wherein Q is -C(O) (CH ₂ ) _p C(0)ORι wherein Ri is hydrogen may be prepared from the corresponding piperazineacetamides of formula (I) wherein X or X' is -(CH ₂ )mNHQ, wherein Q is -C(O) (CH ₂ ) _p C(0)ORι wherein Ri is C ₁ -C ₄ alkyl by techniques and procedures well known in the art, such as acid or base hydrolysis.

The piperazineacetamides of formula (I) wherein X or X' is -(CH ₂ )mNHQ, wherein Q is -C(0)CH=CHC(0)ORι wherein Ri is hydrogen may be prepared from the corresponding piperazineacetamides of formula (I) wherein X or X' is -(CH ₂ )mNHQ, wherein Q is -C(0)CH=CHC(0)ORι wherein Ri is Ci- C ₄ alkyl by techniques and procedures well known in the art, such as acid or base hydrolysis.

The piperazineacetamides of formula (I) wherein X or X' is -(CH ₂ )mNHQ, wherein Q is -(CH ₂ ) _p -C(0)ORι wherein Ri is hydrogen may be prepared from the corresponding piperazine¬ acetamides of formula (I) wherein X or X' is -(CH ₂ )mNHQ, wherein Q is -(CH ₂ ) _p >C(0)ORι wherein Ri is C ₁ -C ₄ alkyl by techniques and procedures well known in the art, such as acid or base hydrolysis.

The piperazineacetamides of formula (I) wherein X or X' is -(CH ₂ ) _m O(CH ₂ ) _p »Z wherein Z is -C(0)ORι wherein Ri is hydrogen may be prepared from the corresponding piperazineacetamides of formula (I) wherein X or X' is

-(CH ₂ ) _m O(CH ₂ ) _p 'Z, wherein Z is -C(0)ORι wherein Ri is C ₁ -C ₄ alkyl by techniques and procedures well known in the art, such as acid or base hydrolysis.

The piperazineacetamides of formula (I) wherein X or X' is -(CH ₂ ) _m C(0)ORι wherein Ri is hydrogen may be prepared from the corresponding piperazineacetamides of formula (I) wherein X or X' is -(CH ₂ ) _m C(0)ORι wherein R _x is C ₁ -C ₄ alkyl by techniques and procedures well known in the art, such as acid or base hydrolysis.

The piperazineacetamides of formula (I) wherein X or X' is -(CH ₂ ) _m NR ₂ R ₃ , wherein R ₂ and R ₃ are hydrogen may be prepared from the corresponding piperazineacetamides of formula (I) where X or X' is -(CH ₂ )mNHQ, wherein Q is ~(CH ₂ ) _P 'C(0)ORι wherein p' is 0 and Ri is t-butyl by techniques and procedures well known in the art, such as acid hydrolysis.

The piperazineacetamides of formula (I) wherein R is C ₁ -C ₄ alkyl and X or X" is -(CH ₂ )mNHQ, wherein Q is -C(0)R ₄ may be prepared from the corresponding piperazineacetamides of formula (I) wherein R is C ₁ -C ₄ alkyl and X or X' is -(CH2) _m NR2*R3 wherein R2 and R3 are hydrogen by techniques and procedures well known and appreciated by one of ordinary skill in the art, such as such as reaction with the appropriate acid chloride of the structure C1-C(0)R ₄ or an appropriate acid anhydride of the structure R ₄ ~C(0)-0- C(0)-R ₄ along with a suitable non-nucleophilic base, such as dimethylaminopyridine, triethylamine or pyridine. For those piperazineacetamides of formula (I) wherein R is hydrogen and X or X' is -(CH ₂ ) _m NR ₂ R ₃ wherein R ₂ and R ₃ are hydrogen, the piperazine amino may be protected prior to the acylation reaction. The selection and utilization of suitable protecting groups is well known by one of ordinary

skill in the art and is described in "Protective Groups in Organic Syntheses", Theodora W. Greene, Wiley (1981). Subsequent deprotection gives the piperazineacetamides of formula (I) wherein R is hydrogen and X or X' is -(CH ₂ )mNHQ, wherein Q is -C(0)R4.

The piperazineacetamides of formula (I) wherein R is C ₁ -C ₄ alkyl and X or X' is -(CH ₂ )mNHQ, wherein Q is -C(O) (CH ₂ ) _p C(0)ORι wherein Ri is C ₁ -C ₄ alkyl may be prepared from the corresponding piperazineacetamides of formula (I) wherein R is C ₁ -C ₄ alkyl and X or X' is -(CH ₂ )mNR ₂ R ₃ wherein R ₂ and R ₃ are hydrogen by techniques and procedures well known and appreciated by one of ordinary skill in the art, such as reaction with the appropriate acid chloride of the structure Cl-C(O) (CH ₂ ) _p C(0)ORι wherein Ri is C ₁ -C ₄ alkyl along with a suitable non-nucleophilic base, such as dimethylaminopyridine, triethylamine or pyridine. For those piperazineacetamides of formula (I) wherein R is hydrogen and X or X* is -(CH ₂ ) _m NR ₂ R ₃ wherein R ₂ and R ₃ are hydrogen, the piperazine amino may be protected prior to the acylation reaction. The selection and utilization of suitable protecting groups is well known by one of ordinary skill in the art and is described in "Protective Groups in Organic Syntheses", Theodora W. Greene, Wiley (1981). Subsequent deprotection gives the piperazineacetamides of formula (I) wherein R is hydrogen and X or X" is -(CH ₂ )mNHQ, wherein Q is -C(O) (CH ₂ ) _p C(0)ORι wherein Ri is C ₁ -C ₄ alkyl.

The piperazineacetamides of formula (I) wherein R is C ₁ -C ₄ alkyl and X or X' is -(CH ₂ )mNHQ, wherein Q is

-C(0)CH=CHC(0)ORι wherein Ri is C ₁ -C ₄ alkyl may be prepared from the corresponding piperazineacetamides of formula (I) wherein R is C ₁ -C ₄ alkyl and X or X ¹ is -(CH ₂ ) _m NR ₂ R ₃ wherein R ₂ and R3 are hydrogen by techniques and procedures well known and appreciated by one of ordinary skill in the art.

such as reaction with the appropriate acid chloride of the structure Cl-C(0)CH=CHC(0)ORι wherein Ri is C ₁ -C ₄ alkyl along with a suitable non-nucleophilic base, such as dimethylaminopyridine, triethylamine or pyridine. For those piperazineacetamides of formula (I) wherein R is hydrogen and X or X' is -(CH2) _m NR2*R3 wherein R ₂ and R ₃ are hydrogen, the piperazine amino may be protected prior to the acylation reaction. The selection and utilization of suitable protecting groups is well known by one of ordinary skill in the art and is described in "Protective Groups in Organic Syntheses", Theodora W. Greene, .Wiley (1981). Subsequent deprotection gives the piperazineacetamides of formula (I) wherein R is hydrogen and X or X' is -(CH ₂ )mNHQ, wherein Q is -C(0)CH=CHC(0)ORι wherein Ri is C ₁ -C ₄ alkyl. The piperazineacetamides of formula (I) wherein X or X' is may be prepared

from the corresponding piperazineacetamides of formula (I) wherein X or X' is -(CH ₂ ) _m CN by techniques and procedures well known and appreciated by one of ordinary skill in the art and described in J. Med. Chem., 33, 317 1990.

The piperazineacetamides of formula (I) ^{may be} P ^re Pared

the corresponding piperazineacetamides of formula (I) wherein X or X' is -(CH ₂ ) _m CN by techniques and procedures well known and appreciated by one of ordinary skill in the art, such as reaction with sodium azide and ammonium chloride.

The piperazineacetamides of formula (I) wherein X or X ¹ is -(CH ₂ )mO(CH ₂ ) _p -Z wherein Z is OH may be prepared from the corresponding piperazineacetamides of formula (I) wherein X or X' is -(CH ₂ )mO(CH ₂ ) _p >Z

wherein Z is by techniques and procedures well known and appreciated by one of ordinary skill in the art, such as base hydrolysis.

Starting materials for use in Scheme A are readily available to one of ordinary skill in the art.

The following examples present typical syntheses as described in Scheme A. These examples are understood to be illustrative only and are not intended to limit the scope of the present invention in any way. As used herein, the following terms have the indicated meanings: "g" refers to grams; "mmol" refers to millimoles; "mL" refers to milliliters; "bp" refers to boiling point; "mp" refers to melting point; "°C" refers to degrees Celsius; "mm Hg" refers to millimeters of mercury; "μL" refers to microliters; "yg" refers to micrograms; and "μM" refers to micromolar.

Example 1 N-(3-Diethylaminomethylphenyl)-N-phenyl-4-methyl-l- piperazineacetamide trioxalate

_lc Step a: N-[3-Diethylaminomethylphenyl]-N-phenyl- chloroacetamide .Dissolve N-[3-methylphenyl]-N-phenylamine (20g, O.llmol) in acetonitrile (400mL) and add triethylamine (40mL, 0.33mol).

Cool in an ice-bath and add trifluoroacetic anhydride (23mL, « ₀ 0.165mol). Remove the cooling bath and stir at room temperature for 4 hours under a nitrogen atmosphere.

Evaporate the solvent in υacuo, partition between saturated aqueous sodium hydrogen carbonate and extract with ethyl acetate. Dry (MgS0 ₄ ) and evaporate the solvent in υacuo to ₂₅ give N-[3-methylphenyl]-N-phenyltrifluoroacetamide.

1H NMR (CDC1 ₃ ) δ 2.32 (s, 3H) , 6.95-7.5 (m, 9H); 19F NMR δ 94.8 (s).

Dissolve N-[3-methylphenyl]-N-phenyltrifluoroacetamide

30 (4.8g, 1.7mmol) in carbon tetrachloride (250mL) and add N- bromosuccinimide (6g, 3.4mmol). Reflux with a 175W sunlamp for 48 hours under a nitrogen atmosphere. Cool in an ice- bath and remove the precipitate by filtration. Evaporate ₃₅ the solvent in υacuo and purify by chromatography (80:20

cyclohexane/ethyl acetate) to give N-[3-bromomethylphenyl]- N-phenyltrifluoroacetamide (5.5g, 91%).

1H NMR (CDC1 ₃ ) δ 4.45 (s, 2H) , 7.05-7.65 (m, 9H) ; ¹⁹ F NMR δ 94.8.

Dissolve N-[3-bromomethylphenyl]-N-phenyltrifluoroacetamide (2.18mmol) in excess diethylamine and leave at room temperature for 48 hours. Evaporate the excess diethylamine in υacuo to give N-[3-diethylaminomethylphenyl]-N-phenyl¬ trifluoroacetamide.

Mix N-[3-diethylaminomethylphenyl]-N-phenyltrifluoro¬ acetamide (1.74mmol) in 4:1 ethanol/water and add potassium hydroxide (lOg). Reflux for 2 days, evaporate the solvent in υacuo and take the residue up in water. Extract into ethyl acetate, dry (MgSθ ₄ ) and evaporate the solvent in υacuo to give N-[3-diethylaminomethylphenyl]-N-phenylamine.

Dissolve N-[3-diethylaminomethylphenyl]-N-phenylamine

(38mmol) in acetonitrile (450mL) and add pyridine (4.6mL, 57mmol). Cool in an ice-bath and slowly add chloroacetyl chloride (4.5mL, 57mmol). Remove the cooling bath and stir at room temperature overnight under a nitrogen atmosphere. Evaporate the solvent in υacuo and partition between saturated aqueous sodium hydrogen carbonate and ethyl acetate. Separate the organic phase, dry (MgSθ ₄ ) and evaporate the solvent in υacuo to give the title compound.

Step b: N-(3-Diethylaminomethylphenyl)-N-phenyl-4-methyl-l- piperazineacetamide trioxalate

Dissolve N-[3-diethylaminomethylphenyl]-N-phenylchloro- acetamide (30mmol) in acetonitrile (150mL), add N-methyl- piperazine (12g, 120mmol) and reflux overnight under a nitrogen atmosphere. Evaporate the solvent in υacuo and

partition between saturated aqueous sodium hydrogen carbonate and ethyl acetate. Separate the organic phase, wash with brine, dry (MgSθ ₄ ) and evaporate the solvent in υacuo to give N-(3-diethylaminomethylphenyl)-N-phenyl-4- methyl-1-piperazineacetamide.

Dissolve N(3-diethylaminomethylphenyl)-N-phenyl-4-methyl-l- piperazineacetamide (l.Smmol) in tetrahydrofuran (_50mL) and add a solution of oxalic acid dihydrate (600mg, 4.5mmol) in tetrahydrofuran (20mL). Filter the precipitate and recrystallize (ethanol/water) to give the title compound.

Example 2 N,N-Diphenyl-4-methyl-l-piperazineacetamide dioxalate

Step a: NrN-Diphenylchloroacetamide

Dissolve diphenylamine (38mmol) in acetonitrile (450mL) and add pyridine (4.6mL, 57mmol). Cool in an ice-bath and slowly add chloroacetyl chloride (4.5mL, 57mmol). Remove the cooling bath and stir at room temperature overnight under a nitrogen atmosphere. Evaporate the solvent in υacuo and partition between saturated aqueous sodium hydrogen carbonate and ethyl acetate. Separate the organic phase, dry (MgSθ ₄ ) and evaporate the solvent in υacuo to give the title compound.

Step b: N,N-Diphenyl-4-methyl-l-piperazineacetamide dioxalate

Dissolve N,N-diphenylchloroacetamide (30mmol) in acetonitrile (150mL), add N-methylpiperazine (12g, 120mmol) and reflux overnight under a nitrogen atmosphere. Evaporate the solvent in υacuo and parition between saturated aqueous sodium hydrogen carbonate and ethyl acetate. Separate the organic phase, wash with brine, dry (MgS0 ₄ ) and evaporate the solvent in vacuo to give N,N-diphenyl-4-methyl-l- piperazineacetamide.

Dissolve N,N-diphenyl-4-methyl-l-piperazineacetamide (1.5mmol) in tetrahydrofuran (50mL) and add a solution of oxalic acid dihydrate (400mg, 3mmol) in tetrahydrofuran (15mL). Filter the precipitate and recrystallize (isopropanol/water) to give the title compound.

Example 3 N-[4-(t-Butoxycarbamoyl)phenyl]-N-phenyl-4-methyl-1- piperazineacetamide dioxalate

Step a:. N-[4-t-Butoxycarbamoylphenyl]-N-phenylchloro- acetamide

Dissolve 4-aminodiphenylamine (lOg, 54mmol) in chloroform (lOOmL), add triethylamine (llmL, βlmmol) and cool in an ice-bath. Slowly add a solution of di-tert-butydicarbonate (12g, 54mmol) in chloroform (50mL), remove the ice-bath and stir at room temperature overnight under a nitrogen atmosphere. Evaporate the solvent in υacuo and purify by chromatography (80:20 cyclohexane/ethyl acetate) to give N- [4-t-Butoxycarbamoylphenyl]-N-phenylamine (12g, 80%).

1H NMR (CDCI ₃ ) δ 1.5 (S, 9H), 5.6 (S, 1H), 6.45 (S, 1H), 6.8- 7.35 ( , 9H).

Dissolve N-[4-t-Butoxycarbamoylphenyl]-N-phenylamine (llg, 38mmol) in acetonitrile (450mL) and add pyridine (4.6mL, 57mmol). Cool in an ice-bath and slowly add chloroacetyl chloride (4.5mL, 57mmol). Remove the cooling bath and stir at room temperature overnight under a nitrogen atmosphere. Evaporate the solvent in υacuo and partition between saturated aqueous ^' sodium hydrogen carbonate and ethyl acetate. Separate the organic phase, dry (MgS0 ₄ ) and evaporate the solvent in vacuo . Purify by chromatography (80:20 cyclohexane/ethyl acetate) to give the title compound (llg, 84%).

1H NMR (CDCI ₃ ) δ 1.5 (S, 9H), 4 (s, 2H) , 6.7 (s, 1H), 7.1-7.5 (m, 9H).

Step b: N[4-(t-Butoxycarbamoyl)phenyl3-N-phenyl-4-methyl-l- piperazineacetamide dioxalate

Dissolve N-[4-t-Butoxycarbamoylphenyl]-N-phenylchloro- acetamide (llg, 30mmol) in acetonitrile (150mL), add N- methylpiperazine (12g, 120mmol) and reflux overnight under a nitrogen atmosphere. Evaporate the solvent in υacuo and

partition between saturated aqueous sodium hydrogen carbonate and ethyl acetate. Separate the organic phase, wash with brine, dry (MgS0 ₄ ) and evaporate the solvent in υacuo to give N[4-(t-Butoxycarbamoyl)phenyl]-N-phenyl-4- methyl-1-piperazineacetamide (12g, 94%).

1H NMR (CDCI ₃ ) δ 1.5 (s, 9H), 2.25 (s, 3H) , 2.8-2.8 (m, 8H) , 3.05 (s, 2H), 6.6 (S, 1H), 7.05-7.5 (m, 9H) .

Dissolve N[4-(t-Butoxycarbamoyl)phenyl]-N-phenyl-4-methy1-1- piperazineacetamide (1.5mmol) in tetrahydrofuran (50mL) and add a solution of oxalic acid dihydrate (400mg, 3mmol) in tetrahydrofuran (15mL). Filter the precipitate and recrystallize (isopropanol/water) to give the title compound.

Example 4 N-(4-Aminophenyl)-N-phenyl-4-methyl-l-piperazineacetamide dimaleate

Method A:

Dissolve N[4-(t-Butoxycarbamoyl)phenyl]-N-phenyl-4-methy1-1- piperazineacetamide (6g, 14mmol) in a 40:60 mixture of methylene chloride/trifluoroacetic acid (200mL), cool in an

ice-bath and stir for 1 hour. Evaporate the solvent in υacuo and partition between saturated aqueous sodium hydrogen carbonate and ethyl acetate. Separate the organic phase, dry (MgSθ ₄ ) and evaporate the solvent in vacuo to give N(4- aminophenyl)-N-phenyl-4-methyl-l-piperazineacetamide (3.5g, 78%).

1H NMR (CDCI ₃ ) δ 2.4 (s, 3H) , 2.5-2.85 (m, 8H) , 3.1 (S, 2H) , 3.4-4 (bs, 2H), 6.65 (d, 2H), 7.03 (d, 2H), 7.1-7.5 (m, 5H).

Dissolve N-4-aminophenyl-N-phenyl-4-methyl-l- piperazineacetamide (500mg, 1.5mmol) in tetrahydrofuran (50mL) and add a solution of maleic acid (348mg, 3mmol) in tetrahydrofuran (20mL). Filter the precipitate and recrystallize (isopropanol/water) to give the title compound.

Method B:

Step a: N-[4-Nitrophenyl1-N-phenylchloroacetamide Dissolve 4-nitrodiphenylamine (38mmol) in toluene (450mL) and add chloroacetyl chloride (4.5mL, 57mmol) . Reflux the mixture overnight under a nitrogen atmosphere. Evaporate the solvent in vacuo and partition between saturated aqueous sodium hydrogen carbonate and ethyl acetate. Separate the organic phase, dry (MgS0 ₄ ) and evaporate the solvent in vacuo to give the title compound.

Step b: N-4-Aminophenyl-N-phenyl-4-methyl-l-piperazine- acetamide dimaleate

Dissolve N-[4-nitrophenyl]-N-phenylchloroacetamide (30mmol) in acetonitrile (150mL), add N-methylpiperazine (12g, 120mmol) and reflux overnight under a nitrogen atmosphere. Evaporate the solvent in υacuo and partition between saturated aqueous sodium hydrogen carbonate and ethyl acetate.

Separate the organic phase, wash with brine, dry (MgS0 ₄ ) and evaporate the solvent in υacuo to give N-4-nitrophenyl-N- phenyl-4-methyl-l-piperazineacetamide.

Dissolve N-4-nitrophenyl-N-phenyl-4-methyl-l-piperazine- acetamide (12mmol) in ethanol (lOOmL) and add tin(II) chloride dihydrate (16.3g). Warm to between 65°C and 75°C for 4 to 5 hours. Cool to room temperature and pour into a mixture of ethyl acetate (300mL) and water (200mL). Add solid potassium carbonate and stir occasionally until the carbon dioxide evolution ceases. Filter through filter aid and separate the organic phase. Dry (MgSθ ₄ ) and evaporate the solvent in vacuo to give N-4-aminophenyl-N-phenyl-4- methyl-1-piperazineacetamide.

Dissolve N-4-aminophenyl-N-phenyl-4-methyl-l-piperazine- acetamide (500mg, 1.5mmol) in tetrahydrofuran (50mL) and add a solution of maleic acid (348mg, 3mmol) in tetrahydrofuran (20mL). Filter the precipitate and recrystallize (isopropanol/water) to give the title compound.

Example 5 N-4-Acetamidophenyl-N-phenyl-4-methyl-l-piperazineacetamide dioxalate

Mix N-4-aminophenyl-N-phenyl-4-methyl-l-piperazineacetamide (200mg, 0.6mmol), triethylamine (0.17mL), acetyl chloride (0.045mL), dimethylaminopyridine (5mg) and acetonitrile (lOmL). Stir at room temperature for 24 hours, evaporate the solvent in vacuo and partition between saturated aqueous sodium hydrogen carbonate and ethyl acetate. Separate the organic phase, dry (MgS0 ₄ ) and evaporate the solvent in υacuo to give N-4-acetamidophenyl-N-phenyl-4-methyl-l-piperazine- acetamide.

Dissolve N-4-acetamidophenyl-N-phenyl-4-methyl-l- piperazineacetamide (1.5mmol) in tetrahydrofuran (50mL) and add a solution of oxalic acid dihydrate (400mg, 3mmol) in tetrahydrofuran (15mL). Filter the precipitate and recrystallize (isopropanol/water) to give the title compound.

Example 6 N-2-(t-Butoxycarbamoyl)phenyl-N-phenyl-4-methyl-l- piperazineacetamide dioxalate

Prepare as described above in Example 3 for N-4-(t- Butoxycarbamoyl)phenyl-N-phenyl-4-methyl-l-piperazine- acetamide dioxalate but using 2-aminodiphenylamine instead of 4-aminodiphenylamine.

Example 7 N-3-Hydroxyphenyl-N-phenyl-4-methyl-l-piperazineacetamide dioxalate

Prepare as described above in Example 2 for N,N-diphenyl-4- methyl-1-piperazineacetamide dioxalate but using N-[3- hydroxyphenyl]-phenylamine instead of diphenylamine and using 3 equivalents of chloro acetyl chloride, 3 equivalents of pyridine and 4 equivalents of N-methyl-piperazine (see Example 9).

Prepare as described above in Example 4 for N-4-aminophenyl- N-phenyl-4-methyl-l-piperazineacetamide dioxalate but using N-4-(t-Butoxycarbamoyl)phenyl-N-4'-methoxyphenyl-4-methyl-l- piperazineacetamide instead of N-4-(t-Butoxycarbamoyl)- phenyl-N-phenyl-4-methyl-l-piperazineacetamide.

Example 8 N-3-Methylphenyl-N-phenyl-4-methyl-l-piperazineacetamide dioxalate

Prepare as described above in Example 2 for N,N-diphenyl-4- methyl-1-piperazineacetamide dioxalate but using N-[3- methylphenyl]-phenylamine instead of diphenylamine.

Example 9 N-3-[ (4-Methyl-l-piperazinomethyl)carboxymethyl]phenyl-N- phenyl-4-methyl-l-piperazineacetamide tetraoxalate

Step a: N-[3-[chloromethyl)carboxymethyl]phenyl]-N- phenylchloroacetamide

Mix N-[3-bromomethylphenyl]-N-phenyltrifluoroacetamide (16g, 44mmol), potassium acetate (22g) and dimethylformamide (200mL). Heat to 50°C for 48 hours, add water (200mL) and separate the aqueous phase. Extract the aqueous phase with a mixture of 1:1 ethyl ether/cyclohexane, dry (MgSθ ₄ ) and evaporate the solvent in υacuo to give N-[3-acetoxy-- methylphenyl]-N-phenyltrifluoroacetamide.

Mix N-[3-acetoxymethylphenyl]-N-phenyltrifluoroacetamide (44mmol), potassium carbonate (20g) and a mixture of 1:4 water/methanol (300mL). Stir at room temperature for 24 hours, evaporate the solvent in υacuo and partition between water and ethyl ether. Separate the organic phase, dry (MgSθ ₄ ) and evaporate the solvent in υacuo. Purify by chromatography (2:3 ethyl acetate/cyclohexane) to give N-[3- hydroxymethylphenyl]-N-phenylamine (7.6g).

Dissolve N-[3-hydroxymethylphenyl]-N-phenylamine (38mmol) in acetonitrile (450mL) and add pyridine (9.2mL, 114mmol). Cool in an ice-bath and slowly add chloroacetyl chloride (9mL, 114mmol). Remove the cooling bath and stir at room temperature overnight under a nitrogen atmosphere. Evaporate the solvent in υacuo and partition between saturated aqueous sodium hydrogen carbonate and ethyl acetate. Separate the organic phase, dry (MgS0 ₄ ) and evaporate the solvent in υacuo to give the title compound.

Step b: N-3-[ (4-Methyl-l-piperazinomethyl)carboxymethyl]- phenyl-N-phenyl-4-methyl-l-piperazineacetamide tetraoxalate Dissolve N-[3-[ (chloromethyl)carboxymethyl]phenyl]-N- phenylchloroacetamide (30mmol) in acetonitrile (150mL), add N-methylpiperazine (12g, 120mmol) and reflux overnight under a nitrogen atmosphere. Evaporate the solvent in υacuo and

partition between saturated aqueous sodium hydrogen carbonate and ethyl acetate. Separate the organic phase, wash with brine, dry (MgS0 ₄ ) and evaporate the solvent in vacuo to give N-3-[ (4-methyl-l-piperazinomethyl)carboxy- methyl]phenyl-N-phenyl-4-methyl-l-piperazineacetamide.

Dissolve N-3-[ (4-methyl-l-piperazinomethyl)carboxy- methyl]phenyl-N-phenyl-4-methyl-l-piperazineacetamide (1.5mmol) in tetrahydrofuran (50mL) and add a solution of oxalic acid dihydrate (800mg, 6mmol) in tetrahydrofuran (15mL). Filter the precipitate and recrystallize (ethanol/water) to give the title compound.

Example 10 N-3-Hydroxymethylphenyl-N-phenyl-4-methyl-l-piperazine- acetamide dioxalate

Mix N-3-[ (4-methyl-l-piperazinomethyl)carboxymethylJphenyl- N-phenyl-4-methyl-l-piperazineacetamide (400mg, 0.48mmol), potassium carbonate (2g) and a mixture of 4:1 methanol/water. Stir at room temperature for 24 hours, partition between saturated aqueous sodium hydrogen carbonate and ethyl acetate. Separate the organic phase, dry (MgSθ ₄ ) and evaporate the solvent in vacuo to give N-3- hydroxymethylphenyl-N-phenyl-4-methyl-l-piperazineacetamide.

Dissolve N-3-hydroxymethylphenyl-N-phenyl-4-methyl-l- piperazineacetamide (1.5mmol) in tetrahydrofuran (50mL) and add a solution of oxalic acid dihydrate (400mg, 3mmol) in tetrahydrofuran (15mL). Filter the precipitate and recrystallize (ethanol) to give the title compound.

Example 11 N-3-(l-Imidazoylmethyl)phenyl-N-phenyl-4-methyl-l- piperazineacetamide dioxalate

Step a: N-[3-(1-Imidazoylmethyl)phenyl1-N-phenylchloro- acetamide

Mix N-[3-bromomethylphenyl]-N-phenyltrifluoroacetamide (lg), imidazole (lg) and acetonitrile (lOmL). Reflux for 3 days, evaporate the solvent in vacuo and take the residue up in water. Add sodium hydrogen carbonate and extract into ethyl acetate. Purify by chromatography (8:2 ethyl acetate/methanol) to give N-[3-(1-imidazoylmethy1)phenyl]-N- phenyltrifluoroacetamide.

Mix N-[3-(1-imidazoylmethy1)phenyl]-N-phenyltrifluoro¬ acetamide (600mg) in 4:1 ethanol/water and add potassium hydroxide (lOg). Reflux for 2 days, evaporate the solvent in vacuo and take up the residue in water. Extract into ethyl

acetate, dry (MgS0 ₄ ) and evaporate the solvent in vacuo to give N-[3-(1-imidazoylmethyl)phenyl]-N-phenylamine.

Dissolve N-[3-(1-imidazoylmethyl)phenyl]-N-phenylamine (38mmol) in acetonitrile (450mL) and add pyridine (4.6mL, 57mmol). Cool in an ice-bath and slowly add chloroacetyl chloride (4.5mL, 57mmol). Remove the cooling bath and stir at room temperature overnight under a nitrogen atmosphere. Evaporate the solvent in υacuo and partition between saturated aqueous sodium hydrogen carbonate and ethyl acetate.

Separate the organic phase, dry (MgS0 ₄ ) and evaporate the solvent in vacuo to give the title compound.

Step b: N-3-(l-Imidazoylmethyl)phenyl-N-phenyl-4-methyl-l- piperazineacetamide dioxalate

Dissolve N-[3-(1-imidazoylmethyl)phenyl]-N-phenylchloro- acetamide (30mmol) in acetonitrile (150mL), add N-methyl¬ piperazine (12g, 120mmol) and reflux overnight under a nitrogen atmosphere. Evaporate the solvent in vacuo and partition between saturated aqueous sodium hydrogen carbonate and ethyl acetate. Separate the organic phase, wash with brine, dry (MgSθ ₄ ) and evaporate the solvent in vacuo. Purify by chromatography to give N-3-(l-imidazoyl- methyl)phenyl-N-phenyl-4-methyl-l-piperazineacetamide.

Dissolve N-3-(l-imidazoylmethyl)phenyl-N-phenyl-4-methyl-l- piperazineacetamide (l.Smmol) in tetrahydrofuran (50mL) and add a solution of oxalic acid dihydrate (400mg, 3mmol) in tetrahydrofuran (20mL). Filter the precipitate and recrystallize to give the title compound.

Example 12 N-4-Cyanophenyl-N-phenyl-4-methyl-l-piperazineacetamide dioxalate

Step a: N-[4-Cyanophenyl]-N-phenylchloroacetamide

A mixture of 7.2g (0.04mol) of 4-bromobenzonitrile, 11ml (0.12mol) of aniline, 5.6g (0.04mol) of potassium carbonate and 0.76g (0.004mole) of copper iodide was heated at 150°C for 24 hours. The mixture was taken up in 150ml of water and extracted with ethyl acetate. The organic phase was dried over magnesium sulfate and concentrated in vacuo . The residue was purified by filtration through a path of silica gel eluting with cyclohexane/ethyl acetate: 70/30.

Dissolve N-[4-cyanophenyl]-N-phenylamine (38mmol) in acetonitrile (450mL) and add pyridine (4.6mL, 57mmol). Cool in an ice-bath and slowly add chloroacetyl chloride (4.5mL, 57mmol). Remove the cooling bath and stir at room temperature overnight under a nitrogen atmosphere. Evaporate the solvent in vacuo and partition between saturated aqueous sodium hydrogen carbonate and ethyl acetate. Separate the organic phase, dry (MgS0 ₄ ) and evaporate the solvent in υacuo to give the title compound.

Step b: 4-Cvano-N,N-diphenyl-4-methyl-l-piperazineacetamide trioxalate

Dissolve N-[4-cyanophenyl]-N-phenylchloroacetamide (30mmol) in acetonitrile (150mL), add N-methylpiperazine (12g, 5 120mmol) and reflux overnight under a nitrogen atmosphere. Evaporate the solvent in υacuo and partition between saturated aqueous sodium hydrogen carbonate and ethyl acetate. Separate the organic phase, wash with brine, dry (MgS0 ₄ ) and evaporate the solvent in vacuo . Purify by chromatography to 0 give N-4-cyanophenyl-N-phenyl-4-methyl-l-piperazineacetamide. Dissolve N-4-cyanophenyl-N-phenyl-4-methyl-l-piperazine- acetamide (l.Smmol) in tetrahydrofuran (50mL) and add a solution of oxalic acid dihydrate (400mg, 3mmol) in tetrahydrofuran (20mL). Filter the precipitate and 5 recrystallize (isopropanol/water) to give the title compound.

Example 13 N-(3-Methoxycarbonylmethyl)phenyl-N-phenyl-4-methy1-1- 0 piperazineacetamide dioxalate

Step a:* N-[Methoxycarbonylmethylphenyl]-N-phenylchloro- acetamide

Dissolve N-[3-bromomethylphenyl]-N-phenyltrifluoroacetamide 5 (41.3mmol) in 95% ethanol (40mL) and heat to reflux. Add,

in portions through the reflux condenser, a solution of potassium cyanide (4.3g) in water (6mL). Add additional water (4mL) to effect the transfer. Reflux for 9 hours, pour into water and extract into ethyl ether. Wash with brine, dry (MgSθ ₄ ) and evaporate the solvent in vacuo to give N-[3-cyanomethylphenyl]-N-phenyltrifluoroacetamide.

Mix N-[3-cyanomethylphenyl]-N-phenyltrifluoroacetamide (1.3g) and concentrated hydrochloric acid (lOOmL) and reflux overnight. Dilute with 4:1 ethanol/water and carefully add potassium hydroxide (lOg). Reflux for 2 days, evaporate the solvent in vacuo and take up the residue in water. Extract into ethyl acetate. Dry (MgS0 ₄ ) and evaporate the solvent in vacuo to give N-[3-carboxymethylphenyl]-N-phenylamine.

Dissolve N-(3-Carboxymethylphenyl)-N-phenylamine in a MeOH and trimethoxymethane (1/1) mixture. HCl is bubbled through the mixture for 10 minutes and the mixture is refluxed overnight. The solvent is removed in vacuo, to afford N-(3- methoxycarbonylmethylphenyl)-N-phenylamine.

Dissolve N-[3-methoxycarbonylmethylphenyl]-N-phenylamine (38mmol) in acetonitrile (450mL) and add pyridine (4.6mL, 57mmol). Cool in an ice-bath and slowly add chloroacetyl chloride (4.5mL, 57mmol). Remove the cooling bath and stir at room ^' temperature overnight under a nitrogen atmosphere. Evaporate the solvent in vacuo and partition between saturated aqueous sodium hydrogen carbonate and ethyl acetate. Separate the organic phase, dry (MgS0 ₄ ) and evaporate the solvent in vacuo to give the title compound.

Step b; N-3-Methoxycarbonylmethylphenyl-N-phenyl-4-methyl- 1-piperazineacetamide dioxalate

Dissolve N-[methoxycarbonylmethylphenyl]-N-phenylchloro- acetamide (30mmol) in acetonitrile (150mL), add N-methyl-

piperazine (12g, 120mmol) and reflux overnight under a nitrogen atmosphere. Evaporate the solvent in vacuo and partition between saturated aqueous sodium hydrogen carbonate and ethyl acetate. Separate the organic phase, wash with brine, dry (MgS0 ₄ ) and evaporate the solvent in vacuo . Purify by chromatography to give N-3-methoxy- carbonylmethylphenyl-N-phenyl-4-methyl-l-piperazine- acetamide.

Dissolve N-3-methoxycarbonylmethylphenyl-N-phenyl-4-methyl- 1-piperazineacetamide (l.Smmol) in tetrahydrofuran (50mL) and add a solution of oxalic acid dihydrate (400mg, 3mmol) in tetrahydrofuran (20mL). Filter the precipitate and recrystallize to give the title compound.

Example 14 N-3-Carboxymethylphenyl-N-phenyl-4-methyl-l-piperazine- acetamide dihydrochloride

Dissolve N-3-methoxycarbonylmethylphenyl-N-phenyl-4-methyl- 1-piperazineacetamide (500mg) in 0.1N aqueous hydrochloric acid. Reflux for 4 hours, remove the water in vacuo and recrystallize (isopropanol) to give the title compound.

Example 15 N-3-Dimethylaminocarbonylmethylphenyl-N-phenyl-4-methyl-l- piperazineacetamide dioxalate

Mix 3-carboxymethyl-N,N-diphenylamine (0.34mmol), methylene chloride (120mL) and di ethylformamide (0.05mL) under a nitrogen atmosphere. Add oxalyl chloride (3.5mL, 40mmol) over about 5 minutes with stirring. Stir at ambient temperature for 3 hours. Cool the mixture in an ice bath and bubble dimethylamine into the solution for 10 minutes. Stir the mixture for 1 hour and evaporate the solvent in vacuo. Partition the residue between saturated aqueous sodium hydrogen carbonate and ethyl acetate. Separate the organic phase, wash with brine, dry (MgSθ ₄ ) and evaporate the solvent in vacuo to give 3-dimethylaminocarbonylmethyl- diphenylamine.

The title compound is prepared as described in Example 2 for N,N-diphenyl-4-methyl-l-piperazineacetamide dioxalate but using 3-dimethylaminocarbonylmethyl-diphenylamine instead of diphenylamine.

Example 16 N-4-(t-Butoxycarbamoyl)phenyl-N-4'-methoxyphenyl-4-methyl-l- piperazineacetamide dioxalate

Prepare as described above in Example 3 for N-4-(t- Butoxycarbamoyl)pheny1-N-pheny1-4-methyl-1- piperazineacetamide dioxalate but using N-[4-aminophenyl]-N- [4'-methoxyphenyl]amine instead of 4-aminodiphenylamine.

Example 17

N-4-Aminophenyl-N-4 ' -methoxyphenyl-4-methyl-l-piperazine- acetamide sesσui oxalate

Prepare as described above in Example 4 for N-4-aminophenyl- N-phenyl-4-methyl-l-piperazineacetamide dioxalate but using N-4-(t-Butoxycarbamoyl)phenyl-N-4'-methoxyphenyl-4-methyl-l- piperazineacetamide instead of N-4-(t-Butoxycarbamoyl)- phenyl-N-phenyl-4-methyl-l-piperazineacetamide.

Example 18 N-Phenyl-N-(2-pyridyl)-4-methyl-l-piperazineacetamide dioxalate

Prepare ^' as described above in Example 2 for N,N-diphenyl-4- methyl-1-piperazineacetamide dioxalate but using N-phenyl-N- (2-pyridyl)amine instead of diphenylamine.

Example 19 N-3-Trifluoromethyl-phenyl-N-(2-pyridyl)-4-methyl-l- piperazineacetamide dioxalate

₅ Reduce N-nitroso-N-(2-pyridyl)-3-(trifluoromethyl)aniline with Raney-nickel essentially as described in Organic Synthesis (VI), 542 1988 to give N-3-trifluoromethylphenyl-N-(2- pyridyl)amine.

_Q Prepare the title compound as described above in Example 2 for N,N-diphenyl-4-methyl-l-piperazineacetamide dioxalate but using N-3-trifluoromethylphenyl-N-(2-pyridyl)amine instead of diphenylamine.

5

0

5

Example 20 N,N-di[4-(t-Butoxycarbamoyl)phenyl]-4-methyl-1-piperazine- acetamide dimaleate

Step a: N,N-di[4-t-Butoxycarbamoylphenyl]chloroacetamide Dissolve 4,4'-diaminodiphenylamine (54mmol) in chloroform (lOOmL), add triethylamine (22ml, 162mmol) and cool in an ice-bath. Slowly add a solution of di-tert-butyldicarbonate (24g, lOδmmol) in chloroform (lOOmL), remove the ice-bath and stir at room temperature overnight under a nitrogen atmosphere. Evaporate the solvent in vacuo and purify by chromatography to give N,N-[4,4'-di-t-Butoxycarbamoyl- diphenylamine.

Dissolve N,N-[4,4'-di-t-Butoxycarbamoyldiphenylamine

(38mmol) in acetonitrile (450mL) and add pyridine (4.6mL,

57mmol). Cool in an ice-bath and slowly add chloroacetyl chloride (4.5mL, 57mmol). Remove the cooling bath and stir at room temperature overnight under a nitrogen atmosphere.

Evaporate the solvent in vacuo and partition between saturated aqueous sodium hydrogen carbonate and ethyl acetate.

Separate the organic phase, dry (MgSθ ₄ ) and evaporate the solvent in vacuo. Purify by chromatography to give the title compound.

Step b: N,N-di[4-(t-Butoxycarbamoyl)phenyl]-4-methyl-l- piperazineacetamide dimaleate

Dissolve N,N-di[4-t-Butoxycarbamoylphenyl]chloroacetamide (30mmol) in acetonitrile (150mL), add N-methylpiperazine (12g, 120mmol) and reflux overnight under a nitrogen atmosphere. Evaporate the solvent in υacuo and partition between saturated aqueous sodium hydrogen carbonate and ethyl acetate. Separate the organic phase, wash with brine, dry (MgSθ ₄ ) and evaporate the solvent in υacuo to give N,N-di [4-(t-Butoxycarbamoyl)phenyl]-4-methyl-1-piperazine- acetamide.

Dissolve N,N-di[4-(t-Butoxycarbamoyl)phenyl]-4-methyl-l- piperazineacetamide (1.5mmol) in tetrahydrofuran (50mL) and add a solution of maleic acid (350mg, 3mmol) in tetrahydrofuran (15mL). Filter the precipitate and recrystallize to give the title compound.

Example 21 N,N-di[4-aminophenyl-4-methyl-l-piperazineacetamide dimaleate

Dissolve N,N-di[4-(t-Butoxycarbamoyl)phenyl]-4-methyl-l- piperazineacetamide (14mmol) in a 40:60 mixture of methylene chloride/trifluoroacetic acid (200mL), cool in an ice-bath and stir for 1 hour. Evaporate the solvent in υacuo and

partition between saturated aqueous sodium hydrogen carbonate and ethyl acetate. Separate the organic phase, dry (MgSθ ₄ ) and evaporate the solvent in υacuo to give N,N- di[4-aminophenyl]-4-methyl-l-piperazineacetamide.

Dissolve 4,4'-di[aminophenyl]-4-methyl-l-piperazineacetamide (1.5mmol) in tetrahydrofuran (50mL) and add a solution of maleic acid (350mg, 3mmol) in tetrahydrofuran (20mL). Filter the precipitate and recrystallize (ethanol) to give the title compound.

Example 22 N-4-(t-Butoxycarbamoyl)phenyl-N-phenyl-l-piperazineacetamide dioxalate

Step b: N-4-(t-Butoxycarbamoyl)phenyl-N-phenyl-l- piperazineacetamide dioxalate

Dissolve N-[4-t-Butoxycarbamoylphenyl]-N-phenylchloro- aceta ide (llg, 30mmol) in acetonitrile (150mL), add piperazine (120mmol) and reflux overnight under a nitrogen atmosphere. Evaporate the solvent in υacuo and parition between saturated aqueous sodium hydrogen carbonate and ethyl acetate. Separate the organic phase, wash with brine.

dry (MgSθ ₄ ) and evaporate the solvent in υacuo to give N-4-(t- Butoxycarbamoyl)phenyl-N-phenyl-l-piperazineacetamide.

Dissolve N-4-(t-Butoxycarbamoyl)phenyl-N-phenyl-l- piperazineacetamide (1.5mmol) in tetrahydrofuran (50mL) and add a solution of oxalic acid dihydrate (400mg, 3mmol) in tetrahydrofuran (15mL). Filter the precipitate and recrystallize to give the title compound.

Example 23

N-4-Aminophenyl-N-phenyl-l-piperazineacetamide dimaleate

Dissolve N-4-(t-Butoxycarbamoyl)phenyl-N-phenyl-l- piperazineacetamide (14mmol) in a 40:60 mixture of methylene chloride/trifluoroacetic acid (200mL), cool in an ice-bath and stir for 1 hour. Evaporate the solvent in υacuo and partition between saturated aqueous sodium hydrogen carbonate and ethyl acetate. Separate the organic phase, dry (MgSθ ₄ ) and evaporate the solvent in υacuo to give N-4- aminophenyl-N-phenyl-1-piperazineacetamide.

Dissolve N-4-aminophenyl-N-phenyl-l-piperazineacetamide (500mg, l.Smmol) in tetrahydrofuran (50mL) and add a solution of maleic acid (350mg, 3mmol) in tetrahydrofuran

(20mL). Filter the precipitate and recrystallize to give the title compound.

Example 24 N-3-Chlorophenyl-N-phenyl-4-methyl-l-piperazineaceamide dioxalate

Prepare as described above in Example 2 for N,N-diphenyl-4- methyl-1-piperazineacetamide dioxalate but using 3-chloro- N,N-diphenylamine instead of diphenylamine.

Example 25 N-2-Methoxycarbonylphenyl-N-phenyl-4-methyl-l-piperazine- acetamide dioxalate

Prepare as described above in Example 13 for N-(3-methoxy- carbonylmethylphenyl-N-phenyl-4-methyl-l-piperazineacetamide dioxalate but using N-(2-methoxycarbonylphenyl)-N-phenylamine instead of N-(3-methoxycarbonylmethylphenyl)-N-phenylamine.

Example 26 N-2-Carboxyphenyl-N-phenyl-4-methyl-l-piperazineacetamide dihydrochloride

Prepare as described above in Example 14 for N-(3- carboxymethylphenyl-N-phenyl-4-methyl-l-piperazineacetamide dioxalate but using N-(2-methoxycarbonylmethylphenyl-N- phenyl-4-methyl-l-piperazineacetamide instead of N-(3- methoxycarbonylmethylphenyl-N-phenyl-4-methyl-l-piperazine- acetamide.

Example 27 NrN-di[4-methoxyphenyl]-4-methyl-l-piperazineacetamide dioxalate

*° prepare as described above in Example 2 for N,N-diphenyl-4- methyl-1-piperazineacetamide dioxalate but using 4,4'- dimethoxy-N,N-diphenylamine instead of diphenylamine.

Example 28 ™ N-3-Trifluoromethylphenyl-N-phenyl-4-methyl-l-piperazine- acetamide dioxalate

Prepare as described above in Example 2 for N,N-diphenyl-4- methyl-1-piperazineacetamide dioxalate but using 3- 35 trifluromethyl-N,N-diphenylamine instead of diphenylamine.

Example 29 N-4-Sulfophenyl-N-phenyl-4-methyl-l-piperazineacetamide dihydrochloride

Step a: N-4-Sulfophenyl-N-phenylchloroacetamide Dissolve diphenylamine-4-sulfonic acid (lOmmol) in acetonitrile (lOOmL) and add pyridine (40mmol). Cool in an ice bath and slowly add chloroacetyl chloride (3.1mL, 40mmol). Remove the cooling bath and stir at room temperature overnight under a nitrogen atmosphere. Add saturated aqueous sodium hydrogen carbonate and stir vigorously for 3 hours. Evaporate the solvent in vacuo, acidify the residue with IN hydrochloric acid and add ethyl acetate. Separate the organic phase, dry (MgS0 ₄ ) and evaporate the solvent in vacuo to give the title compound.

Step b: N-4-Sulfophenyl-N-phenyl-4-methyl-l-piperazine- acetamide dihydrochloride

Dissolve N-4-sulfophenyl-N-phenylchloroacetamide (5mmol) in acetonitrile (75mL), add N-methyl piperazine (1.2g, 12mmol) and reflux overnight under a nitrogen atmosphere. Evaporate the solvent in υacuo, take the residue up in water and place on a column of ion exchange resin. Elute with water followed by IN hydrochloric acid. Evaporate the water from

the acidic phase and recrystallize (ethanol) to give the title compound.

Example 30 N-3-Methoxyphenyl-N-phenyl-4-methyl-l-piperazineacetamide dioxalate

Prepare as described above in Example 2 for N,N-diphenyl-4- methyl-1-piperazineacetamide dioxalate but using 3-methoxy- N,N-diphenylamine instead of diphenylamine.

Example 31 N-2-Fluorophenyl-N-(2-pyrinyl)-4-methyl-l-piperazine- acetamide dioxalate

Prepare as described above in Example 2 for N,N-diphenyl-4- methyl-1-piperazineacetamide dioxalate but using N-2-fluoro- phenyl-N-(2-pyridyl)amine instead of diphenylamine.

Example 32

N,N-di-[ 4-methylphenyl ]-4-methyl-l-piperazineacetamide dioxalate

Prepare as described above in Example 2 for N,N-diphenyl-4- methyl-1-piperazineacetamide dioxalate but using 4,4'- dimethyl-N,N-diphenylamine instead of diphenylamine.

Example 33 N-4-Propionamidophenyl-N-phenyl-4-methyl-l-piperazine- acetamide dioxalate

Prepare as described above in Example 2 for N,N-diphenyl-4- methyl-1-piperazineacetamide dioxalate but using 4- propionamido-N,N-diphenylamine instead of diphenylamine.

Example 34 N-4-Maleamidophenyl-N-phenyl-4-methyl-l-piperazineacetamide diformate

Prepare as described above in Example 5 for 4-acetamido-N,N- diphenyl-4-methyl-l-piperazineacetamide dioxalate but using maleic anhydride instead of acetyl chloride; the title

Example 35 N-4-Isopropylaminophenyl-N-phenyl-4-methyl-l-piperazine- acetamide dioxalate

Prepare as described above in Example 54 for N-4-methyl- aminophenyl-N-phenyl-4-methyl-l-piperazineacetamide dioxalate but using 4-isopropylamino-N,N-diphenylamine instead of N-[4-methylaminophenyl]-N-phenylamine.

Example 36

N-4- (p-Toluenesulfamido)phenyl-N-diphenyl-4-methyl-l- piperazineacetamide dioxalate

Prepare as described above in Example 2 for N,N-diphenyl-4- methyl-1-piperazineacetamide dioxalate but using 4-(p- toluenesulfamido)-N,N-diphenylamine instead of diphenylamine.

Alternatively, prepare as described above in Example 5 for N-4-acetamidophenyl-N-phenyl-4-methyl-l-piperazineacetamide dioxalate but using p-toluenesulfonylchloride instead of acetylchloride.

Example 37 N-4-(2-Tetrazoyl)phenyl-N-phenyl-4-methyl-l-piperazine- acetamide dioxalate

Mix N-4-cyanophenyl-N-phenyl-4-methyl-l-piperazineacetamide (59.4mmol), sodium azide (3.9g, 59.4mmol), ammonium chloride (3.2g, 59.4mmol) and dimethylformamide (30mL). Heat at 115- 120°C for 4 hours. Cool and add another 3 equivalents of both sodium azide and ammonium chloride. Heat an additional 18 hours at 115-120°C. Pour into water (500mL) and extract with ethyl acetate. Separate the organic phase and wash repeatedly with water then a brine solution. Dry (MgSθ ₄ ) and evaporate the solvent in υacuo . Purify by chromatography

to give N-4-(2-tetrazoyl)phenyl-N-phenyl-4-methyl-l- piperazineacetamide.

Dissolve N-4-(2-tetrazoyl)phenyl-N-phenyl-4-methyl-l- piperazineacetamide (l.Smmol) in tetrahydrofuran (50mL) and add a solution of oxalic acid dihydrate (400mg, 3mmol) in tetrahydrofuran (15mL). Filter the precipitate and recrystallize to give the title compound.

compound is purified by reversed phase HPLC (H ₂ 0, CH ₃ CN, HCOOH) followed by recrystallization.

Example 38 N-3-(t-Butoxycarbonyl)methoxyphenyl-N-phenyl-4-methyl-l- piperazineacetamide dioxalate

Step a: N-[3-(t-butyloxycarbonylmethoxy)phenyl1-N- phenylchloroacetamide

Mix 3-hydroxy-diphenylamine (3.7g, 20mmol), potassium carbonate (8.3g), o-bromo-tert-butylacetate (3.22mL, 22mmol) and acetone (40mL). Reflux for 24 hours, add water and ethyl ether and separate the organic phase. Dry (MgSOή) and

evaporate the solvent in υacuo to give 3-(t-butoxycarbonyl- methoxy)-diphenylamine.

Dissolve 3-(t-butoxycarbonylmethoxy)-diphenylamine (38mmol) in acetonitrile (450mL) and add pyridine (4.6mL, 57mmol). Cool in an ice-bath and slowly add chloroacetyl chloride (4.5mL, 57mmol). Remove the cooling bath and stir at room temperature overnight under a nitrogen atmosphere. Evaporate the solvent in υacuo and partition between saturated aqueous sodium hydrogen carbonate and ethyl acetate.

Separate the organic phase, dry (MgS0 ₄ ) and evaporate the solvent in υacuo to give the title compound.

Step b: N-3-(t-Butoxycarbonyl)methoxyphenyl-N-phenyl-4- methyl-1-piperazineacetamide dioxalate

Dissolve N-[3-(t-butoxycarbonylmethoxy)phenyl]-N- phenylchloroacetamide (30mmol) in acetonitrile (150mL), add N-methylpiperazine (12g, 120mmol) and reflux overnight under a nitrogen atmosphere. Evaporate the solvent in υacuo and partition between saturated aqueous sodium hydrogen carbonate and ethyl acetate. Separate the organic phase, wash with brine, dry (MgSθ ₄ ) and evaporate the solvent in υacuo to give N-3-(t-butoxycarbonyl)methoxyphenyl-N-phenyl-4- methyl-1-piperazineacetamide.

Dissolve N-3-(t-butoxycarbonyl)methoxyphenyl-N-phenyl-4- methyl-1-piperazineacetamide (l.Smmol) in tetrahydrofuran (50mL) and add a solution of oxalic acid dihydrate (400mg, 3mmol) in tetrahydrofuran (15mL). Filter the precipitate and recrystallize to give the title compound.

Example 39 N-4-Carboxymethoxyphenyl-N-phenyl-4-methyl-l-piperazine- acetamide dioxalate

Mix N-3-(t-butoxycarbonyl)methoxyphenyl-N-phenyl-4-methyl-l- piperazineacetamide (500mg) and oxalic acid (200mg) in water and heat for 2 hours. Evaporate the water in υacuo and recrystallize the residue (isopropanol) to give the title compound.

Example 40

N-3- ( 2-Diethylamino) ethoxyphenyl-N-phenyl-4-methyl-l- piperazineacetamide trioxalate

Step a: N-[3-(2-Diethylaminoethoxy)phenyl]-N-phenyl- chloroacetamide

Suspend lithium aluminum hydride (2.3g, 60mmol) in tetrahydrofuran (150mL) and add, by dropwise addition, a solution of 3-(t-butoxycarbonylmethoxy)-diphenylamine (15g, SOmmol) in tetrahydrofuran (50mL). Maintain reflux for 1 hour, cool and slowly add a mixture of Na ₂ Sθ ₄ »10H ₂ θ (15g) and filter aid (15g). Stir the mixture overnight, filter through filter aid and evaporate the solvent in υacuo to give N-[3-(2-hydroxyethoxy)phenyl]-N-phenylamine.

Dissolve carbon tetrabromide (869mg, 2.62mmol) in methylene chloride (7mL) and add a solution of triphenylphosphine (687mg, 2.62mmol) in methylene chloride (6mL). Stir for 15 minutes and add a solution of N-[3-(2-hydroxyethoxy)phenyl]- N-phenylamine (500mg, 2.18mmol) in methylene chloride (7mL). Stir for 48 hours and add additional triphenylphosphine (2.62mmol) and carbon tetrabromide (2.62mmol). Stir overnight and purify by chromatography (20% ethyl acetate/hexane) to give N-[3-(2-bromoethoxy)phenyl]-N- phenylamine.

Dissolve N-[3-(2-bromoethoxy)phenyl]-N-phenylamine in diethylamine and leave at room temperature for 48 hours. Evaporate the diethylamine in υacuo - extract into ethyl acetate and evaporate the solvent in υacuo to give N-[3-(2- diethylaminoethoxy)phenyl]-N-phenylamine.

Dissolve N-[3-(2-diethylaminoethoxy)phenyl]-N-phenylamine (38mmol) in acetonitrile (450mL) and add pyridine (4.6mL, 57mmol). Cool in an ice-bath and slowly add chloroacetyl chloride (4.5mL, 57mmol). Remove the cooling bath and stir at room temperature overnight under a nitrogen atmosphere. Evaporate the solvent in υacuo and partition between saturated aqueous sodium hydrogen carbonate and ethyl acetate.

Separate the organic phase, dry (MgS0 ₄ ) and evaporate the solvent in υacuo . Purify by chromatography to give the title compound.

Step b: N-3-(2-Diethylamino)ethoxyphenyl-N-phenyl-4-methyl- 1-piperazineacetamide trioxalate

Dissolve N-[3-(2-diethylaminoethoxy)phenyl]-N-phenylchloro- acetamide (30mmol) in acetonitrile (150mL), add N-methyl¬ piperazine (12g, 120mmol) and reflux overnight under a nitrogen atmosphere. Evaporate the solvent in υacuo and partition between saturated aqueous sodium hydrogen carbonate and ethyl acetate. Separate the organic phase, wash with brine, dry (MgS0 ₄ ) and evaporate the solvent in υacuo to give N-3-(2-diethylamino)ethoxyphenyl-N-phenyl-4- methyl-1-piperazineacetamide.

Dissolve N-3-(2-diethylamino)ethoxyphenyl-N-phenyl-4-methyl- 1-piperazineacetamide (l.Smmol) in tetrahydrofuran (50mL) and add a solution of oxalic acid dihydrate (600mg, 4.5mmol) in tetrahydrofuran (15mL). Filter the precipitate and recrystallize to give the title compound.

Example 41 N-3-[2-( (4-Methyl-l-piperazinomethyl)carboxy)ethoxy]phenyl- N-phenyl-4-methyl-l-piperazineacetamide tetraoxalate

Step a: N-[3-(2-( (4-Methyl-l-piperazinomethyl)carboxy)- ethoxy])phenyl]-N-phenylchloroacetamide Dissolve N-[3-(2-hydroxyethoxy)phenyl]-N-phenylamine (38mmol) in acetonitrile (450mL) and add pyridine (9.2mL, 114mmol) . Cool in an ice-bath and slowly add chloroacetyl chloride (9mL, 114mmol). Remove the cooling bath and stir at room temperature overnight under a nitrogen atmosphere. Evaporate the solvent in υacuo and partition between saturated aqueous sodium hydrogen carbonate and ethyl acetate. Separate the organic phase, dry (MgS0 ₄ ) and evaporate the solvent in υacuo. Purify by chromatography to give the title compound.

Step b: N-3-[2-( (4-Methyl-l-piperazinomethyl)carboxy)- ethoxy]phenyl-N-phenyl-4-methyl-l-piperazineacetamide tetraoxalate

Dissolve N-[3-(2-( (4-methyl-l-piperazinomethyl)carboxy)- ethoxy])phenyl]-N-phenylchloroacetamide (30mmol) in acetonitrile (150mL), add N-methylpiperazine (24g, 240mmol) and reflux overnight under a nitrogen atmosphere. Evaporate the solvent in vacuo and partition between saturated aqueous sodium hydrogen carbonate and ethyl acetate. Separate the organic phase, wash with brine, dry (MgS0 ₄ ) and evaporate the solvent in vacuo to give N-3-[2-( (4-methyl-l-piperazino- methyl)carboxy)ethoxy]phenyl-N-phenyl-4-methyl-l-piperazine- acetamide.

Dissolve N-3-[2-( (4-methyl-l-piperazinomethyl)carboxy)- ethoxy]phenyl-N-phenyl-4-methyl-l-piperazineacetamide (l.Smmol) in tetrahydrofuran (50mL) and add a solution of oxalic acid dihydrate (800mg, 6mmol) in tetrahydrofuran (15mL). Filter the precipitate and recrystallize to give the title compound.

Example 42 N-3-(2-Hydroxyethoxy)-N,N-diphenyl-4-methyl-l-piperazine- acetamide dioxalate

Mix N-3-[2-( (4-methyl-l-piperazinomethyl)carboxy)- ethoxy]phenyl-N-phenyl-4-methyl-l-piperazineacetamide (44mmol), potassium carbonate (20g) and a mixture of 1:4 water/methanol (300mL). Stir at room temperature for 24 hours, evaporate the solvent in υacuo and partition between water and ethyl ether. Separate the organic phase, dry (MgS0 ₄ ) and evaporate the solvent in υacuo to give N-3-(2- hydroxyethoxy)phenyl-N-phenyl-4-methyl-l-piperazine- acetamide.

Dissolve N-3-(2-hydroxyethoxy)phenyl-N-phenyl-4-methyl-l- piperazineacetamide (l.Smmol) in tetrahydrofuran (50mL) and add a solution of oxalic acid dihydrate (400mg, 3mmol) in tetrahydrofuran (15mL). Filter the precipitate and recrystallize to give the title compound.

Example 43 N-4-Methylqlutaramidophenyl-N-phenyl-4-methyl-l-piperazine- acetamide dioxalate

Mix N-4-aminophenyl-N-phenyl-4-methyl-l-piperazineacetamide (200mg, O.βmmol), triethylamine (0.17mL), methyl glutaryl chloride (0.6mmol), dimethylaminopyridine (5mg) and acetonitrile (lOmL). Stir at room temperature for 24 hours, evaporate the solvent in vacuo and partition between saturated aqueous sodium hydrogen carbonate and ethyl acetate. Separate the organic phase, dry (MgS0 ₄ ) and evaporate the solvent in vacuo to give N-4-methylglutaramido-phenyl-N- phenyl-4-methyl-l-piperazineacetamide.

Dissolve N-4-methylglutaramidophenyl-N-phenyl-4-methyl-l- piperazineacetamide (1.5mmol) in tetrahydrofuran (50mL) and add a solution of oxalic acid dihydrate (400mg, 3mmol) in tetrahydrofuran (15mL). Filter the precipitate and recrystallize (isopropanol/water) to give the title compound.

Example 44 N-4-Methylsuccinamidophenyl-N-phenyl-4-methyl-l-piperazine- acetamide dioxalate

Mix N-4-aminophenyl-N-phenyl-4-methyl-l-piperazineacetamide (200mg, 0.6mmol), triethylamine (0.17mL), methyl succinyl chloride (0.6mmol), dimethylaminopyridine (5mg) and acetonitrile (lOmL). Stir at room temperature for 24 hours, evaporate the solvent in vacuo and partition between saturated aqueous sodium hydrogen carbonate and ethyl acetate.

Separate the organic phase, dry (MgS0 ₄ ) and evaporate the solvent ^' in vacuo to give N-4-methylsuccinamidophenyl-N-phenyl- 4-methyl-l-piperazineacetamide.

Dissolve N-4-methylsuccinamidophenyl-N-phenyl-4-methyl-l- piperazineacetamide (l.Smmol) in tetrahydrofuran (50mL) and add a solution of oxalic acid dihydrate (400mg, 3mmol) in tetrahydrofuran (15mL). Filter the precipitate and recrystallize (isopropanol/water) to give the title compound.

Example 45 N-4-Pyrrolidinophenyl-N-phenyl-4-methyl-l-piperazine- acetamide trioxalate

Step a: N-4-Pyrrolidinophenyl-N-phenylchloroacetamide Mix 4-aminodiphenylamine (500mg, 2.7mmol), 1,4-dibromobutane (0.32mL, 2.7mmol), potassium carbonate (2g) and dimethylformamide. Heat at 80°C overnight, cool to room temperature and add water (20mL). Separate the aqueous phase and extract with a 1:1 mixture of ethyl ether/cyclohexane. Combine the organic phases, dry (MgSθ ₄ ) and evaporate the solvent in υacuo . Purify by chromatographjy (20:80 ethyl acetate/cyclohexane) to give 4-pyrrolidino- diphenylamine (400mg).

Dissolve 4-pyrrolidino-diphenylamine (38mmol) in acetonitrile (450mL) and add pyridine (4.6mL, 57mmol). Cool in an ice-bath and slowly add chloroacetyl chloride (4.5mL, 57mmol). Remove the cooling bath and stir at room temperature overnight under a nitrogen atmosphere. Evaporate the solvent in υacuo and partition between saturated aqueous sodium hydrogen carbonate and ethyl acetate. Separate the organic phase, dry (MgS0 ₄ ) and evaporate the solvent in υacuo to give the title compound.

Step b: N-4-Pyrrolidinophenyl-N-phenyl-4-methyl-l- piperazineacetamide trioxalate

Dissolve 4-pyrrolidino-N,N-Diphenylchloroacetamide (30mmol) in acetonitrile (150mL), add N-methylpiperazine (12g, 120mmol) and reflux overnight under a nitrogen atmosphere. Evaporate the solvent in υacuo and partition between saturated aqueous sodium hydrogen carbonate and ethyl acetate. Separate the organic phase, wash with brine, dry (MgS0 ₄ ) and evaporate the solvent in υacuo to give N-4-pyrrolidinophenyl- N-phenyl-4-methyl-l-piperazineacetamide.

Dissolve N-4-pyrrolidinophenyl-N-phenyl-4-methyl-l- piperazineacetamide (l.Smmol) in tetrahydrofuran (50mL) and add a solution of oxalic acid dihydrate (600mg, 4.5mmol) in tetrahydrofuran (15mL). Filter the precipitate and recrystallize (ethanol/water) to give the title compound.

Example 46 N-4-(2-lH-Imidazoyl)phenyl-N-phenyl-4-methyl-l-piperazine- acetamide dioxalate

Mix N-4-cyanophenyl-N-phenyl-4-methyl-l-piperazineacetamide (113mmol), sulfur (1.9g, 0.06mol), 2-methoxyethanol (lOOmL) and ethylene diamine (8.4g, 0.14mol) and heat at 130°C for 5

hours. Dilute with IN hydrochloric acid and wash with ethyl acetate. Neutralize the aqueous phase with potassium carbonate and extract into ethyl acetate. Dry (MgSθ ₄ ) and evaporate the solvent in υacuo to give N-4-[2-(4,5-dihydro)- IH-imidazole]phenyl-N-phenyl-4-methyl-l-piperazineacetamide.

Heat a mixture of Mnθ ₂ (7.5g, 85mmol) and benzene (50mL) for 2 hours, collecting any water present in a Dean-Stark trap. Cool, decant the benzene and add a solution of N-4-[2-(4,5- dihydro)-IH-imidazole]phenyl-N-phenyl-4-methyl-l-piperazine- acetamide (7.2mmol) in methylene chloride (30mL). Stir for 6 days, filter and extract with methylene chloride in a Soxhlet apparatus for 24 hours. Combine the organic extracts and evaporate the solvent in vacuo to give N-4-(2-lH- imidazole)phenyl-N-phenyl-4-methyl-l-piperazineacetamide.

Dissolve N-4-(2-lH-imidazole)phenyl-N-pheny1-4-methyl-l- piperazineacetamide (l.Smmol) in tetrahydrofuran (50mL) and add a solution of oxalic acid dihydrate (400mg, 3mmol) in tetrahydrofuran (20mL). Filter the precipitate and recrystallize to give the title compound.

Example 47 N-6-(t-Butoxycarbamoyl-3-pyridyl)-N-phenyl-4-methyl-l- piperazineacetamide dioxalate

Step a: N-[6-(t-Butoxycarbamoyl)-3-pyridyl]-N-phenyl- chloroacetamide

Dissolve 2-amino-5-bromopyridine (54mmol) in chloroform (lOOmL), add triethylamine (llmL, δlmmol) and cool in an ice-bath. Slowly add a solution of di-tert-butyldicarbonate (12g, 54mmol) in chloroform (50mL), remove the ice-bath and stir at room temperature overnight under a nitrogen atmosphere. Evaporate the solvent in vacuo and purify by chromatography to give 2-(t-Butoxycarbamoyl)-5- bromopyridine.

Suspend sodium amide (208mmol) in aniline (20ml) and add, by dropwise addition, t-butanol at room temperature. Heat at 45-50°C for 2 hours. Add a solution of 2-(t-Butoxy¬ carbamoyl)-5-bromopyridine (54mmol) in aniline (20mL) and stir at 40 ^β C for 5 hours. Pour onto cracked ice, extract into ethyl ether and dry (MgS0 ₄ ). Evaporate the solvent in υacuo togive N-6-[t-Butoxycarbamoyl-3-pyridyl]-N-phenylamine.

Dissolve N-6-[t-Butoxycarbamoyl-3-pyridyl]-N-phenylamine (38mmol) in acetonitrile (450mL) and add pyridine (4.6mL, 57mmol). Cool in an ice-bath and slowly add chloroacetyl chloride (4.5mL, 57mmol). Remove the cooling bath and stir at room temperature overnight under a nitrogen atmosphere. Evaporate the solvent in υacuo and partition between saturated aqueous sodium hydrogen carbonate and ethyl acetate. Separate the organic phase, dry (MgS0 ₄ ) and evaporate the solvent in υacuo. Purify by chromatography to give the title compound.

Step b: N-6-[t-Butoxycarbamoyl-3-pyridyl]-N-phenyl-4- methyl-1-piperazineacetamide dioxalate

Dissolve N-[6-(t-Butoxycarbamoyl)-3-pyridyl]-N-phenylchloro- acetamide (30mmol) in acetonitrile (150mL), add N-methyl¬ piperazine (12g, 120mmol) and reflux overnight under a nitrogen atmosphere. Evaporate the solvent in υacuo and parition between saturated aqueous sodium hydrogen carbonate and ethyl acetate. Separate the organic phase, wash with brine, dry (MgS0 ₄ ) and evaporate the solvent in υacuo to give N-6-[(t-Butoxycarbamoyl)3-pyridyl]-N-phenyl-4-methyl-l- piperazineacetamide.

Dissolve N-6-[t-Butoxycarbamoyl-3-pyridyl]-N-pheny1-4- methyl-1-piperazineacetamide (1.5mmol) in tetrahydrofuran (50mL) and add a solution of oxalic acid dihydrate (400mg, 3mmol) in tetrahydrofuran (15mL). Filter the precipitate and recrystallize to give the title compound.

Example 48 N-[6-Amino-3-pyridyl-N-phenyl-4-methyl-l-piperazineacetamide trioxalate

Dissolve N-6-[t-Butoxycarbamoyl-3-pyridyl]-N-pheny1-4- methyl-1-piperazineacetamide (14mmol) in a 40:60 mixture of methylene chloride/trifluoroacetic acid (200mL), cool in an ice-bath and stir for 1 hour. Evaporate the solvent in υacuo and partition between saturated aqueous sodium hydrogen carbonate and ethyl acetate. Separate the organic phase, dry (MgS0 ₄ ) and evaporate the solvent in υacuo to give N-6- [amino-3-pyridyl]-N-phenyl-4-methyl-l-piperazineacetamide.

Dissolve N-[6-amino-3-pyridyl]-N-pheny1-4-methy1-1- piperazineacetamide (l.Smmol) in tetrahydrofuran (50mL) and add a solution of oxalic acid dihydrate (600mg, 4.5mmol) in tetrahydrofuran (20mL). Filter the precipitate and recrystallize to give the title compound.

Example 49 N-[6-t-Butoxycarbamoyl-2-pyridyl]-N-phenyl-4-methyl-l- piperazineacetamide dioxalate

Step a: N-[6-(t-Butoxycarbamoyl)-2-pyridyl]-N-phenylchloro- acetamide

Mix 2,6-diaminopyridine (5.5g, 50mmol), bromobenzene (lOmmol, 1.05mL), potassium carbonate (1.5g) and Cul (0.2g). Heat at 180 ^β C for 24 hours under a nitrogen atmosphere. Purify by chromatography (3:1 ethyl acetate/cyclohexane) to give N-[6-amino-2-pyridyl]-N-phenylamine. Dissolve N-[6-amino-2-pyridyl]-N-phenylamine (54mmol) in chloroform (lOOmL), add triethylamine (llmL, βlmmol) and cool in an ice-bath. Slowly add a solution of di-tert- butyldicarbonate (12g, 54mmol) in chloroform (50mL), remove the ice-bath and stir at room temperature overnight under a nitrogen atmosphere. Evaporate the solvent in υacuo and purify by chromatography to give N-[6-(t-Butoxycarbamoyl)- 2-pyridyl]-N-phenylamine.

Dissolve N-[6-(t-Butoxycarbamoyl)-2-pyridyl]-N-phenylamine (38mmol) in acetonitrile (450mL) and add pyridine (4.6mL, 57mmol) . Cool in an ice-bath and slowly add chloroacetyl chloride (4.5mL, 57mmol). Remove the cooling bath and stir

at room temperature overnight under a nitrogen atmosphere. Evaporate the solvent in vacuo and partition between saturated aqueous sodium hydrogen carbonate and ethyl acetate. Separate the organic phase, dry (MgS0 ₄ ) and evaporate the solvent in vacuo . Purify by chromatography to give the title compound.

Step b: N-6-[t-Butoxycarbamoyl-2-pyridyl]-N-phenyl-4- methyl-1-piperazineacetamide dioxalate Dissolve N-[6-(t-Butoxycarbamoyl)-2-pyridyl]-N-phenyl- chloroacetamide (30mmol) in acetonitrile (150mL), add N- methylpiperazine (12g, 120mmol) and reflux overnight under a nitrogen atmosphere. Evaporate the solvent in vacuo and partition between saturated aqueous sodium hydrogen carbonate and ethyl acetate. Separate the organic phase, wash with brine, dry (MgSθ ₄ ) and evaporate the solvent in vacuo to give N-6-[t-Butoxycarbamoyl-2-pyridyl]-N-phenyl-4- methyl-1-piperazineacetamide.

Dissolve N-6-[t-Butoxycarbamoyl-2-pyridyl]-N-phenyl-4- methyl-1-piperazineacetamide (1.5mmol) in tetrahydrofuran (50mL) and add a solution of oxalic acid dihydrate (400mg, 3mmol) in tetrahydrofuran (15mL). Filter the precipitate and recrystallize to give the title compound.

Example 50 N-[6-Amino-2-pyridyl]-N-phenyl-4-methyl-l-piperazine- acetamide trioxalate

Dissolve N-6-[t-Butoxycarbamoyl-2-pyridyl]-N-pheny1-4- methyl-1-piperazineacetamide (14mmol) in a 40:60 mixture of methylene chloride/trifluoroacetic acid (200mL), cool in an ice-bath and stir for 1 hour. Evaporate the solvent in vacuo and partition between saturated aqueous sodium hydrogen carbonate and ethyl acetate. Separate the organic phase, dry (MgSθ ₄ ) and evaporate the solvent in vacuo to give N-6- [amino-2-pyridyl]-N-phenyl-4-methyl-l-piperazineacetamide.

Dissolve N-[6-amino-2-pyridyl]-N-phenyl-4-methyl-l- piperazineacetamide (l.Smmol) in tetrahydrofuran (50mL) and add a solution of oxalic acid dihydrate (600mg, 4.5mmol) in tetrahydrofuran (20mL). Filter the precipitate and recrystallize to give the title compound.

Example 51 N-3-Dimethylaminosulfonylphenyl-N-phenyl-4-methyl-l- piperazineacetamide dioxalate

Dissolve N,N-diphenylamino-3-sulfonic acid-piperazine- acetamide (40mmol) in methylene chloride (200mL). Cool to 0°C, place under a nitrogen atmosphere and add, by dropwise addition, thionyl chloride (5.28g, 44mmol). Stir at room temperature for several hours and evaporate the solvent in vacuo to give 3-chlorosulfonyl-N,N-diphenylamine.

Dissolve dimethylamine hydrochloride (0.67mmol) in saturated sodium hydrogen carbonate (3mL). Add a solution of 3- chlorosulfonyl-N,N-diphenylamine(0.34mmol) in acetone (3mL) and stir at room temperature under an argon atmosphere for 30 minutes. Adjust to pH 6 with saturated sodium hydrogen carbonate and extract into ethyl ether. Dry (MgS0 ₄ ) and evaporate the solvent in υacuo to give 3-dimethylamino- sulfonyl-N,N-diphenylamine.

N-3-dimethylaminosulfonylphenyl-N-phenyl-4-methyl-l-piper a- ineacetamide dioxalate is prepared as described above in example 2 for N,N-diphenyl-4-methyl-l-piperazine acetamide dioxalate but using 3-dimethylammosulfonyl-N,N-diphenylamine instead of diphenylamine.

Example 52 N-4-Methylaminophenyl-N-phenyl-4-methyl-l-piperazine- acetamide dioxalate

Step a: N-[4-(N'-methyl-t-Butoxycarbamoyl)phenyl]-N- Phenylchloroacetamide

Suspend lithium aluminum hydride (170mg) in tetrahydrofuran and add, by dropwise addition, a solution of N-[4-t-Butoxy- carbamoylphenyl]-N-phenylamine (500mg) in tetrahydrofuran (20mL). Reflux for 2 hour, cool to 0°C and add Na ₂ Sθ ₄ »10H ₂ θ and filter aid until no further reaction is observed. Stir the mixture overnight, filter through filter aid and evaporate the solvent in υacuo to give N-[4-methylamino- phenyl]-N-phenylamine.

Dissolve N-[4-methylaminophenyl]-N-phenylamine (54mmol) in chloroform (lOOmL), add triethylamine (llraL, βlmmol) and cool in an ice-bath. Slowly add a solution of di-tert- butyldicarbonate (12g, 54mmol) in chloroform (50mL), remove the ice-bath and stir at room temperature overnight under a nitrogen atmosphere. Evaporate the solvent in υacuo and purify by chromatography (80:20 cyclohexane/ethyl acetate) to give N-[4-( '-methyl-t-Butoxycarbamoyl)phenyl]-N-phenylamine.

Dissolve N-[4-( '-methyl-t-Butoxycarbamoyl)phenyl]-N- phenylamine (38mmol) in acetonitrile (450mL) and add

pyridine (4.6mL, 57mmol). Cool in an ice-bath and slowly add chloroacetyl chloride (4.5mL, 57mmol). Remove the cooling bath and stir at room temperature overnight under a nitrogen atmosphere. Evaporate the solvent in vacuo and partition between saturated aqueous sodium hydrogen carbonate and ethyl acetate. Separate the organic phase, dry (MgS0 ₄ ) and evaporate the solvent in vacuo . Purify by chromatography to give the title compound.

Step b: N-4-Methylaminophenyl-N-phenyl-4-methyl-l- piperazineacetamide dioxalate

Dissolve N-[4-(N ^• -methyl-t-Butoxycarbamoyl)phenylJ-N- phenylchloroacetamide (30mmol) in acetonitrile (150mL), add N-methylpiperazine (12g, 120mmol) and reflux overnight under a nitrogen atmosphere. Evaporate the solvent in vacuo and partition between saturated aqueous sodium hydrogen carbonate and ethyl acetate. Separate the organic phase, wash with brine, dry (MgS0 ₄ ) and evaporate the solvent in vacuo to give N-4-(N'-methyl-t-butoxycarbamoyl)phenyl-N- phenyl-4-methyl-l-piperazineacetamide.

Dissolve N-4-(N*-methyl-t-Butoxycarbamoyl)phenyl-N-pheny1-4- methyl-1-piperazineacetamide (14mmol) in a 40:60 mixture of methylene chloride/trifluoroacetic acid (200mL), cool in an ice-bath and stir for 1 hour. Evaporate the solvent in vacuo and partition between saturated aqueous sodium hydrogen carbonate and ethyl acetate. Separate the organic phase, dry (MgS04) and evaporate the solvent in vacuo to give N-4- methylaminophenyl-N-phenyl-4-methyl-l-piperazineacetamide.

Dissolve N-4-methylaminophenyl-N-phenyl-4-methyl-l- piperazineacetamide (l.Smmol) in tetrahydrofuran (50mL) and add a solution of oxalic acid dihydrate (400mς, 3mmol) in tetrahydrofuran (20mL). Filter the precipitate and recrystallize to give the title compound.

The compounds of the present invention are antimuscarinic agents, some of which have a selectivity for the Mi receptor. "Mi selectivity" means about a 5 fold greater potency at displacing selectively bound ligands from cloned Mi receptors compared individually to other subtypes of cloned muscarinic receptors; preferably, there is a 50 fold difference and more preferably a 100 fold difference in the potency.

Some examples of compounds of the present invention which are believed to possess good Mi selectivity are 4- amino-N,N-diphenyl-4-methyl-l-piperazineacetamide and N, N- diphenyl-4-methyl-l-piperazineacetamide.

Any appropriate test may be used in order to determine the affinity of the compounds of Formula I to muscarinic receptors or of specific subtypes of muscarinic receptors. For example, to determine muscarinic receptor subtype affinity, pellets from cells A9L-mι, A9L-m ₂ , A9L-πt ₃ , A9L-πi ₄ or CHO-ms which express, respectively, πtι _f m ₂ , πt ₃ , ιr ₄ , or ms receptor subtypes, which are stored frozen at -80°C, are thawed and homogenized in 10 ml of ice-cold 50 mM K/NaPθ ₄ buffer (pH 7.4) using a Polytron (setting 6 for 15 s). The homogenate is centrifuged at 18,000 rpm (40,000 g) in a Beckman centrifuge, rotor JA20 for 10 minutes at 4°C. The pellet is resuspended in the same buffer in order to have 0.5-2 mg protein/ml buffer. The incubation tubes contain 700 μl buffer, 100 μl atropine sulfate (2.10-6 M final) or test compound, 100 μl 3H-NMS ([3H]-N-methyl-scopolamine) (0.3 nM final) and 100 μl of homogenate. After a 1 hour incubation at room temperature, each incubation is terminated by rapid filtration through Whatman GF/B glass fiber filters, presoaked in water, using a Brandel cell harvester. The filters are rinsed 3 times with 5 ml 0.9% sodium chloride. The filters are transfered to

scintillation vials and 10 ml of scintillation fluid (Quicksafe A) is added. The filters are counted by liquid scintillation spectrometry. Specific binding of 3H-NMS is measured as the excess over blanks taken in the presence of 2.10-6 M atropine sulfate. Protein content of the membranes is determined by the method of J. Biol. Chem. 193:265-275 (1951). Displacement curves are analyzed using the EBDA/LIGAND (Elsevier Biosoft) program to obtain Hill slopes and IC ₅₀ values. The Ki value is determined with the Cheng-Prusoff equation of Biochem. Pharmacol. 22:3099-3108 (1973) incorporated herein by reference.

The compounds of Formula I are useful in the treatment of Parkinson's disease. Parkinson's disease is a clinical syndrome comprised of bradykinesia, muscular rigidity, resting tremor and abnormalities of posture and gait. It afflicts approximately 1% of all adults over the age of 65 and usually is manifested after the age of 55. Without treatment, the patient succumbs to the disease typically due to complications of immobility such as pulmonary embolism, aspiration or hypostatic pneumonias. Its cause remains unknown, but it is generally responsive to anticholinergic and dopaminergic agents. It has been shown that many currently used anticholinergic antiparkinsonian drugs bind at various muscarinic receptors, for example see Pharmacology & Toxicology 62:90-94 (1988) incorporated herein by reference.

One method of demonstrating the use of the compounds of Formula I for the treatment of Parkinson's disease is found in the articles Pycock, C. J., Neuroscience, 5:461-514 (1980) and ϋngerstedt, J., Acta Physiol. Scand. (Supp.) 367:69-93 (1971) incorporated herein by reference.

The treatment of a patient with Parkinson's disease with the compounds of Formula I is effected by administering to the patient an effective amount of a compound or combination of compounds of Formula I, preferably in combination with a pharmaceutically acceptable carrier, in order to treat the disease. This "effective amount" will vary with the extent of the disease state; the condition of the patient; variables between patients such as age, weight, concurrent medications taken, and concurrent disease states; and any other known factors typically considered when dosing medications. Typically, the compounds of Formula I used to treat Parkinsons's disease range from about 0.01 mg/kg to about 15 mg/kg.

The compounds of Formula I are useful in the treatment of motion sickness. Motion sickness is a disorder typically caused by repetitive angular, linear or vertical motion and is manifested in symptoms primarily of nausea and vomiting. Antimuscarinic agents have been tested in emesis models to show effectiveness in the control of vomiting, for example see Neuropharmacology 27(9) :949-956 (1988). Antimuscarinics have also been shown useful in post-operative nausea and vomiting, and drug (such as opiate) induced nausea and vomiting. See Mitchelson, F., Drugs 43(3) :295-315 (1992) incorporated herein by reference.

One method of demonstrating the use of the compounds of Formula I for the treatment of motion sickness is found in the article Lucot, J., Pharm. Biochem.& Behavior, 32:207-210 (1989) incorporated herein by reference. In another reference for a method used to test relief of symptoms of motion sickness, adult suncus murinus were subjected to slow horizontal rotary motion for 10 minutes. The number of retches and/or vomits were counted in the absence or presence of a test compound administered 30 minutes before

subjection to motion. Reference: Ueno et al.. Life Sciences 43:413-420, 1988.

The treatment of _a patient with motion sickness with the compounds of the present invention is effected by administering to the patient an effective amount of a compound or combination of compounds of Formula I, preferably in combination with a pharmaceutically acceptable carrier, in order to treat the condition. This "effective amount" will vary with the extent of the disease state; the condition of the patient; variables between patients such as age, weight, concurrent medications taken, and concurrent disease states; and any other known factors typically considered when dosing medications. Typically, the compounds of Formula I used to treat motion sickness range from about 0.01 mg/kg to about 15 mg/kg. It is typical that the treatment of motion sickness also includes prophylactic treatment and it is preferably administered by transdermal administration.

The compounds of the present invention also inhibit the secretion of gastric acid. "Inhibition of gastric acid secretion" means to control gastric acidity by reducing the amount of gastric acid typically secreting by that individual. An example of a disease in which inhibition of gastric acid secretion is desirable is peptic ulcer disease. Patients with peptic ulcer disease generally have increased perietal cell mass, elevated basal and stimulated gastric acid and pepsin secretion, impaired suppression of gastrin release when the gastric contents are acidic, rapid gastric emptying, and/or a more acidic duodenal bulbar pH. Even though peptic ulcer disease is typically multi- factorial, therapy directed towards reduction of gastric acid secretion has proven effective. Antimuscarinic agents, particularly Mi antimuscarinic agents, have been

shown to inhibit gastric acid secretion, for example see European Journal of Pharmacology, 112:211-224 (1985) incorporated herein by reference. In this reference, isolated mouse stomachs were perfused from pyloric cannula with unbuffered mucosal solution and the pH of the perfusate detected continuously using a pH meter. The effect of carbachol, in the presence or absence of an antagonist, on pH values were expressed as nmol HVmin.

The treatment of a patient in need of an inhibition of gastric acid secretion with the compounds of the present invention is effected by administering to the patient an effective amount of a compound or combination of compounds of Formula I, preferably in combination with a pharmaceutically acceptable carrier, in order to treat the condition. This "effective amount" will vary with the extent of the disease state; the condition of the patient; variables between patients such as age, weight, concurrent medications taken, and concurrent disease states; and any other known factors typically considered when dosing medications. Typically, the amount of compounds of Formula I used to treat a patient in need of inhibition of gastric acid secretion is from about 0.01 mg/kg to about 15 mg/kg per day.

The duration of treatment using the compounds of formula I is highly variable and can be ascertained by those skilled in the art. The preferred route of administration is oral administration. For oral administration the formula I compounds can be formulated into solid or liquid preparations such as capsules, pills, tablets, troches, lozenges, melts, powders, solutions, suspensions, or emulsions. The solid unit dosage forms can be a capsule which can be of the ordinary hard- or soft- shelled gelatin type containing, for example, surfactants.

lubricants, and inert fillers such as lactose, sucrose, calcium phosphate, and cornstarch. In another embodiment the compounds of this invention can be tableted with conventional tablet bases such as lactose, sucrose, and cornstarch in combination with binders such as acacia, cornstarch, or gelatin, disintegrating agents intended to assist the break-up and dissolution of the tablet following administration such as potato starch, alginic acid, corn starch, and guar gum, lubricants intended to improve the flow of tablet granulations and to prevent the adhesion of tablet material to the surfaces of the tablet dies and punches, for example, talc, stearic acid, or magnesium, calcium, or zinc stearate, dyes, coloring agents, and flavoring agents intended to enhance the aesthetic qualities of the tablets and make them more acceptable to the patient. Suitable excipients for use in oral liquid dosage forms include diluents such as water and alcohols, for example, ethanol, benzyl alcohol, and the polyethylene alcohols, either with or without the addition of a pharmaceutically acceptable surfactant, suspending agent, or emulsifying agent.

The Formula I compounds of this invention may also be administered parenterally, that is, subcutaneously, intravenously, intramuscularly, or interperitoneally, as injectable dosages of the compound in a physiologically acceptable diluent with a pharmaceutical carrier which can be a sterile liquid or mixture of liquids such as water, saline, aqueous dextrose and related sugar solutions, an alcohol such as ethanol, isopropanol, or hexadecyl alcohol, glycols such as propylene glycol or polyethylene glycol, glycerol ketals such as 2,2-dimethyl-l,3-dioxolane-4- methanol, ethers such as polyethylene glycol 400, an oil, a fatty acid, a fatty acid ester or glyceride, or an acetylated fatty acid glyceride with or without the

addition of a pharmaceutically acceptable surfactant such as a soap or a detergent, suspending agent such as pectin, carbomers, methylcellulose, hydroxypropylmethylcellulose, or carboxymethylcellulose, or emulsifying agent and other pharmaceutically acceptable adjuvants. Illustrative of oils which can be used in the parenteral formulations of this invention are those of petroleum, animal, vegetable, or synthetic origin, for example, peanut oil, soybean oil, sesame oil, cottonseed oil, corn oil, olive oil, petrolatum, and mineral oil. Suitable fatty acids include oleic acid, stearic acid, and isostearic acid. Suitable fatty acid esters are, for example, ethyl oleate and isopropyl myristate. Suitable soaps include fatty alkali metal, ammonium, and triethanolamine salts and suitable detergents include cationic detergents, for example, dimethyl dialkyl ammonium halides, alkyl pyridinium halides; anionic detergents, for example, alkyl, aryl, and olefin sulfonates, alkyl, olefin, ether, and monoglyceride sulfates, and sulfosuccinates; nonionic detergents, for example, fatty amine oxides, fatty acid alkanolamides, and polyoxyethylenepolypropylene copolymers; and amphoteric detergents, for example, alkyl beta-aminopropionates, and 2-alkylimidazoline quarternary ammonium salts, as well as mixtures. The parenteral compositions of this invention will typically contain from about 0.5 to about 25% by weight of the formula I compound in solution. Preservatives and buffers may also be used advantageously. In order to minimize or eliminate irritation at the site of injection, such compositions may contain a non-ionic surfactant having a hydrophile-lipophile balance (HLB) of from about 12 to about 17. The quantity of surfactant in such formulations ranges from about 5 to about 15% by weight. The surfactant can be a single component having the above HLB or can be a mixture of two or more components having the desired HLB. Illustrative of surfactants used

in parenteral formulations are the class of polyethylene sorbitan fatty acid esters, for example, sorbitan monooleate and the high molecular weight adducts of ethylene oxide with a hydrophobic base, formed by the condensation of propylene oxide with propylene glycol.

The compounds of this invention can also be administered topically. This can be accomplished by simply preparing a solution of the compound to be administered, preferably using a solvent known to promote transdermal absorption such as ethanol or dimethyl sulfoxide (DMSO) with or without other excipients. Preferably topical administration will be accomplished using a patch either of the reservoir and porous membrane type or of a solid matrix variety.

Some suitable transdermal devices are described in U.S. Patent Nos. 3,742,951, 3,797,494, 3,996,934, and 4,031,894. These devices generally contain a backing member which defines one of its face surfaces, an active agent permeable adhesive layer defining the other face surface and at least one reservoir containing the active agent interposed between the face surfaces. Alternatively, the active agent may be contained in a plurality of microcapsules distributed throughout the permeable adhesive layer. In either case, the active agent is delivered continuously from the reservoir or microcapsules through a membrane into the active agent permeable adhesive, which is in contact with the skin or mucosa of the recipient. If the active agent is absorbed through the skin, a controlled and predetermined flow of the active agent is administered to the recipient. In the case of microcapsules, the encapsulating agent may also function as the membrane.

In another device for transdermally administering the compounds in accordance with the present invention, the pharmaceutically active compound is contained in a matrix

from which it is delivered in the desired gradual, constant and controlled rate. The matrix is permeable to the release of the compound through diffusion or microporous flow. The release is rate controlling. Such a system, which requires no membrane is described in U.S. Patent No. 3,921,636. At least two types of release are possible in these systems. Release by diffusion occurs when the matrix is non-porous. The pharmaceutically effective compound dissolves in and diffuses through the matrix itself. Release by microporous flow occurs when the pharmaceutically effective compound is transported through a liquid phase in the pores of the matrix.

For pharmacological end-use applications, the compounds of Formula I are preferentially administered in the form of their pharmaceutically acceptable acid addition salts. Compounds of Formula I can form pharmaceutically acceptable salts with any non-toxic organic or inorganic acid. Illustrative inorganic acids which form suitable salts include hydrochloric, hydrobromic, sulphuric and phosphoric acid and acid metal salts such as sodium monohydrogen orthophosphate and potassium hydrogen sulfate. Illustrative organic acids which form suitable salts include the mono, di and tricarboxylic acids. Illustrative of such acids are, for example, acetic, glycolic, lactic, pyruvic, malonic, succinic, glutaric, fumaric, malic, tartaric, citric, ascorbic, maleic, hydroxymaleic, benzoic, hydroxybenzoic, phenylacetic, cinnamic, salacylic, 2- phenoxybenzoic and sulfonic acids such as methane sulfonic, trifluoromethane sulfonic, 2-hydroxyethane sulfonic acid and p-toluenesulfonic acid.