Anti-inflammatory compounds

Description

This patent application is a continuation of prior application No. 10/298,390, filed Nov. 18, 2002, now abandoned which was in turn a divisional of application No. 10/041,423 filed Jan. 8, 2002 now U.S. Pat. No. 6,509,369 which was a divisional of application No. 09/221,254 filed Dec. 28, 1998, now U.S. Pat. No. 6,372,779 which claims benefit of provisional application No. 60/068,928 filed Dec. 29, 1997.

BACKGROUND OF THE INVENTION

1. Field of Invention

This invention relates to triphenylpropanamide compounds which are useful in treating inflammations but which do not demonstrate the side effects normally associated with other anti-inflammatory treatments such as glucocorticoids This invention also relates to methods for making and using the compounds of the invention.

2. Prior Art

Glucocorticoids are the only agents which reduce all the symptoms that are manifested in chronic adrenocortical disorder and hyperfunction, allergies, rheumatoid arthritis, lupus, inflammatory bowel disease, pneumonia, bronchial asthma, hematological disorders, dermatitis and eczema. Glucocorticoids also reduce immunological response in organ transplants. The undesired side effects of these agents include hypertension, atherosclerosis, diabetes, hyperglycemia, bone thinning and electrolyte imbalance.

Mechanistically, glucocorticoids bind to the glucocorticoid receptor (GR) on the surface of leukocytes and the resulting glucocorticoid -GR complex migrates into the cell nucleus. There, the complex interacts with transcription factor AP-1 (activating protein-1), inhibiting its induction of genes that produce inflammatory cytokines and collagenase, thereby repressing the inflammatory process. However, the complex also activates GRE (glucocorticoid response element), a transcriptional activator of genes which are responsible for the undesirable side effects mentioned heretofore. The most desirable antiinflammatory medication would inhibit AP-1 without activating GRE.

Steroids, such as dexamethasone and prednisone have been found to exhibit potent antiinflammatory activity, but also exhibit the previously-mentioned side effects.

Heretofore, there has been no antiinflammatory agent found which does not cause side effects. Thus, new chemical agents are needed which would have the desired antiinflammatory effect without causing the side effects mentioned above.

Prior art compounds which relate to the triphenylcyclopropyl and triphenylpropyl compounds of the invention are as follows: U.S. Pat. No. 3,941,833 (Gognaco) describes certain amino derivatives of 2,2-diaryl-cyclopropane. They are described as being useful for the treatment of disorders of the cardiovascular system. They are intended for systemic use. There is no indication in this patent that such compounds can or should be administered topically. Nor is there any indication that such compounds would be useful for treating inflammation of the skin.

Gilbert, et al. in J. Med. Chem. 1983, 26, 693–699 report triphenylpropylidene amines and nitrites as inhibitors of prostaglandin synthetase

Blank et al. in J. Med. Chem. 1969, 12, 873–876 describe the inhibition by 2,3,3-triphenylpropylamines of the biosynthesis of aldosterone without altering deoxycorticosterone or corticosterone levels.

Schultz et al. in J. Med. Chem. 1967, 10, 717–724 describe diphenylpropanamides which are hypocholesteremic in rats and inhibit penicillin excretion in dogs

Burch et al. in Proc. Natl. Acad. Sci. USA 1991, 88, 355–359 describe fluorenyl propanamides which inhibit localized inflammatory reactions in mice.

German Patent No. 2,726,993 (Gognaco) describes 1-substituted 2,2-diphenylcydaopropanes. The patent indicates that they are useful as vasodilators and blood pressure loeIn agents. They are intendjed for systemic use. There is no indication in this patent that such compounds can or should be administered topically. Nor is there any indication that such compounds would be useful for treating inflammation of the skin.

Belgian patent No. BE 855689 (Hexachemie S. A. Fr.) describes 2,2-diphenylcyclopropyl methylamides with vasodilator activity.

Precigoux. et al. describe the compound 4,4′-(3Acetemido-2-phenylpropylideee) diphenol diacetate in Acta Crystallogr., Sect. C: Cryst. Struct. Commun., C41 (8), 1985, pp. 1244–1246.

Falkenstein et al. describe certain phenylaziridine compounds in “Single electro transfer versus nucleophilic ring opening in reactions of cistrns pairs of activated 2-pheytaziridines. Strong influence of nitrogen pyramid for N-benzoylaziridines.”, J. Org. Chem., 1993, 58, pp. 7377–7381.

Stamm et al. describe other aziridines in “Reactions with aziridines.53. Arene hydrides. 9. Intermediate substitution in the formation of a benzylic anion by an aromatic radical anion as observed with 1-benzoyl-2-phenylaziridine.”Chem. Ber., 1990, 123, pp. 2227–2230. Stamm et al. also described related aziridine structures in “Reductive ring opening of N-benzoylaziridine by anthracene hydride (anion of 9,10-dihydroanthracene) via base-induced fragmentation of the intermediate carbonyl adduct.” J. Org. Chem., 1989, 54, pp. 1603–1607. However, none of these publications describe the structures of this invention nor do they indicate that such compounds would be useful in treating inflammation.

Therefore, it is an object of this invention to provide one or more compounds capable of treating inflammatory diseases.

It is a further object of this invention to provide compounds capable of treating inflammatory diseases without causing side effects similar to those caused by glucocorticoids.

It is yet another object of this invention to provide a method of making compounds for treating inflammatory diseases.

Another object of this invention is to provide a method of treating inflammatory diseases in mammals by administration of the compounds of this invention.

SUMMARY OF THE INVENTION

This invention relates to novel non-steroidal small molecule organic compounds that exhibit the beneficial therapeutic properties of glucocorticoids, that may be free of glucooorticoidlike side effects, and which may have a high affinity for the human glucocorticoid receptor (hGR). The compounds of this invention have the following structure (I):

wherein X, R¹, R², R³, R⁴, R⁵, W, Y and Z are as defined hereinafter. These compounds are useful in treating inflammatory diseases in humans and other mammals. The compounds of the present invention may also be useful in the treatment of other disorders, such as chronic adrenocortical disorder and hyperfunction, allergies, rheumatoid arthritis, lupus, use as immunosuppressants in organ transplant, pneumonia, bronchial asthma, hematological disorders, dermatitis and eczema. The present invention is also directed to pharmaceutical compositions containing the compounds of formula I and methods of treating inflammation and other conditions employing such compounds.

As used herein unless otherwise noted, alkyl and alkoxy, whether used along or as part of a substituent group, include straight and branched chains. For example, alkyl radicals include methyl, ethyl, propyl, isopropyl, nbutyl, isobutyl, secbutyl, tbutyl, n-pentyl, 2-pentyl, 2-methylbutyl, neopentyl, n-hexyl, 2-hexyl, 2-methylpentyl, etc. Alkoxy radicals are oxygen ethers formed from the previously described straight or branched chain alkyl groups. Of course, if the alkyl or alkoxy substiteent is branched there must be at least three carbon atoms in the group.

The term “aryl” as used herein along or in combination with other terms indicates aromatic hydrocarbon groups such as phenyl or naphthyl. The term heteroaryl means aromatic groups, incorporating as part of the aromatic ring, 1 or 2 hetero atoms selected from any of S, O, or N. With reference to substituents, the term O independently means that when more than one of such substituent is possible such substituents may be the same or different from each other.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

The present invention is directed to compounds of the general formula I:

X may be a single bond or is chosen from hydrogen, sulfur or NR⁵; wherein R⁵ is selected from the group consisting of: hydrogen; alkyl; cycloalkyl; alkenyl; alkynyl; phenyl, in which said phenyl group is substituted with hydrogen or from one to three substituent groups each selected from the group consisting of lower alkyl (C₂–C₆), lower alkoxy, hydroxy, halo, carboxy, caboalkoxy, amino, amido, sulfonamido, or nitrile; phenyl lower alkyl in which said phenyl group is substituted with hydrogen or with from one to three substitent groups each selected from the group consisting of lower alkyl, lower alkoxy, hydroxy, halo, carboxy, carboalkoxy, amino, amido, sulfonamido or nitie. X may further be selected from —(CH₂)_n wherein n is an integer from 1 to 3; —HC═CH—; and —CH_xW wherein W may be oxygen, sulfur or NR⁵. Of course when X is hydrogen, it does not represent a connection between the phenyl rings;

wherein R¹ is from one to three substituent groups each selected from the group consisting of lower alkyl (C₂–C₆), lower alkoxy, hydroxy, halogen such as chlorine, fluorine, iodine or the like, carboxy, carboalkoxy, amino, amido, sulfonamido or nitrile;

wherein R² is a phenyl group in which said phenyl group is substituted with hydrogen or from one to three substituent groups each selected from the group consisting of lower alkyl(C2–C₆), lower alkoxy, hydroxy, halo, carboxy, carboalkoxy, amino, amido, sulonamido or nitrile; or a heteroaromatic ring such as substituted- or unsubstituted thiophene, furan, pyrrole, pyridine, or the like;

wherein Y is —CH₂— or hydrogen;

wherein R³ is chosen from the group consisting of hydrogen; alkyl; cycdoalkyl; alkenyl; alkynyl; phenyl in which said pheyl group is substitited with hydrogen or from one to three substituent groups each selected from the group consisting of lower alkyl, lower alkoxy, hydroxy, halo, carboxy, carboalkoxy, amino, amido, sulfonamido or nitrile; phenylloweralkyl in which said phenyl group is substituted with hydrogen or with one to three substituent groups each selected from the group consisting of lower alkyl, lower alkoxy, hydroxy, halo, carboxy, carboalkoxy, amino, amido, sulfonamido or nitrile;

wherein Z is selected from the group consisting of carbonyl; carboxy; carbonylamino; or sulfone; and

wherein R⁴ is straight- or branched-chain alkyl having from 2 to 12 carbon atoms; phenylloweralkyl in which said phenyl group is substituted with hydrogen or with one to three substituent groups each selected from the group consisting of lower alkyl, lower alkoxy, hydroxy, halo, carboxy, carboalkoxy, amino, amido, sulfonamido or nitrile; a heteroaromatic ring such as substitutedor unsubstituted thiophene, furan, pyrrole, pyridine, or the like or a heteroaromatic ring connected by a lower alkyl chain wherein said heteroaromatic ring is chosen from substituted-or unsubstituted thiophene, furan, pyrrole, pyridine or the like. When X is hydrogen, S or NR⁵, R⁴ may be phenyl wherein said phenyl group is substituted with hydrogen or with one to three substituent groups each selected from the group consisting of lower alkyl, lower alkoxy, hydroxy, halo, carboxy, carboalkoxy, amino, amido, sulfonamido or nitrile.

Preferably, the compounds of this invention have formula (I) above wherein X is hydrogen and Y is hydrogen. Also preferable are the compounds of this invention wherein R¹ is selected from the group consisting of hydrogen and halogen. More preferably, R¹ is fluorine.

More preferably, the compounds of this invention have formula (I) above wherein X is hydrogen, Y is hydrogen, R¹ is selected from the group consisting of hydrogen and halogen and R² is selected from the group consisting of phenyl, halophenyl, or methylenedioxy. Most preferably, R¹ is fluorine or hydrogen and R² is 4chlorophenyl, 4-lodophenyl or 3,4methylendioxyphenyl.

Also preferable are compounds of formula (I) wherein X is hydrogen, Y is hydrogen, R¹ is selected from the group consisting of hydrogen and halogen, R² is selected from the group consisting of phenyl, halophenyl, or alkoxyphenyl and R³ is selected from the group consisting of hydrogen and lower alkyl. Most preferably, R³ is hydrogen.

Another preferable group of compounds of formula (I) are those wherein X is hydrogen, Y is hydrogen, R¹ is selected from the group consisting of hydrogen and halogen, R² is selected from the group consisting of phenyl and halophenyl, R³ is selected from the group consisting of hydrogen and lower alkyl and Z is carbonyl. Preferably, R⁴ is selected from the group consisting of straight-chain alkyl, phenyllower alkyl and heteroaromatic lower alkyl. Even more preferably R⁴ is a heteroaromatic lower alkyl group. Most preferably, R⁴ is 2-thiophenemethylene or 4-chlorophenylmethylene.

The compounds of this invention are useful in treating inflammatory diseases such as rheumatoid arthritis, osteoarthritis, inflammatory bowel disease, dermatitis, and eczema. They may also be therapeutically beneficial in the treatment of other disorders including lupus, chronic adrenal disorder and hyperfunction, allergies, pneumonia, bronchial asthma, hematological disorders and as immunosuppressants in organ transplant. They may be administered topically or systemically.

The compounds of this invention have been found to bind to the hGR. However, because they differ in structure from glucocorticoids, they appear to bind selectively to the hGR, without binding to DNA and activating the GRE. This results in a potentially much lower incidence d side effects, and, consequently, longer periods of administration with greater overall efficacy and relief.

The compounds of this invention are optically active. The beneficial therapeutic activity may reside with either enantiomier or they may be most active and advantageously utilized in racemic mixtures.

Examples of particularly prefeed compounds include: 98, 29, 33, 72, 90, 96, 84, 80, 47, 97, 123, 127, 128, 132, 140, 141, 145, 147, 150, 153, 165, 167, 173, 174, 175, 176, 177, 178, 179, and 180. Exemplary compounds are as follows:

• N-(2-thiophene)acetyl-2,3,3-triphenylpropylamine.
• N-(5-methylthiophene)acetyl-2-phenyl-3,3-bis (4-fluorophenyl)propylamine.
• N-(3-indolyl) acetyl-2,3,3-triphenylpropylamine.
• N-(2-carbonyl-5-methylthiophene)-2-(9H-fluoreny-9-yl)-2-phenylethylamine.
• N-(2-chlorophenyl)acetyl-1,2,2-triphenylcyclopropylmethylamine.
• N-(2-thienyl)carbonyl-1,2,2-triphenylcyclopropylmethylamine.
• N-(phenyloxy)carbonyl-1,2,2-triphenylcyclopropylmethylamine.
• N-(4-chlorophenyloxy)carbonyl-1,2,2-triphenylcyclopropylmethylamine.
• N-(2-pyridine)acetyl-2-(3,4-methylenedioxyphenyl)-3,3-diphenylpropylamine.
• N-(4-n-butoxyphenyl)acetyl-2-(3,4-methylenedioxyphenyl)-3,3-diphenylpropylamine.
• N-(2,4-difluorophenyl)acetyl-2-(3,4-methylenedioxyphenyl)-3,3diphenylpropylamine.
• N-(2-thiophene)carbonyl-2-(3,4-methylenedioxyphenyl)3,3diphenylpropylamine.
• N-(3-cyanophenyl)acetyl-2-(3,4-methylenedioxyphenyl)-3,3-diphelpropylamine.
• N-(2,4ifluorophenyl)carbonyl-2-(3,4-methylenedioxyphenyl)-3,3diphenylpropylamine.
• N-(4-fluorophenyl)acetyl-2- (3,4-methylenedioxyphenyl)3,3-diphenylpropylamine.
• N-(4,5dichlorophenyl)carbonyl-2-(3,4-methylenedioxyphenyl)-3,3-diphenyipropylamine.
• N-(3methylphenyl)acetyl-2-(4-trifluoromethylphenyl)-3,3-diphenylpropylamine.
• N-(phenyl)acetyl-2-(4-trifluoromethylphenyl)-3,3-dipheryipropyiamine.
• N-(5-chloro-2-benzothiophene)acetyl-2-(4-trifluoromethylphenyl)-3,3-diphenylpropylamine.
• N-(2,4-difluorophenyl)carbonyl-2-(4-trifluoromethylphenyl)-3,3-diphenylpropylamine.
• N-(4-trifluoromethylphenyl)acetyl-2-(4-trifluoromethylphenyl)-3,3-diphenylpropylamine.
• N-(phenyl)acetyl-2-(4-trifluoromethylphenyl)-3,3-diphenylpropylamine.
• N-(4-fluorophenyl)acetyl-2-(4-iodomethylphenyl)3,3-diphenylpropylamine.
• N-(3,5-bis-tri fluorophenyl)carbonyl-2-(4-iodomethylphenyl)-3,3-diphenylpropylamine.
• N-(4-chlorophenyl)carbonyl-2-(4-iodomethylphenyl)-3,3-diphenylpropylamine.
• N-(3,4-dichlorophenyl)carbonyl-2-(4-iodomethylphenyl-3,3-diphenylpropylamine.
• N-(2-fluorophenyl)carbonyl-2-(4-iodomethylphenyl)-3,3-diphenylpropylamine.
• N-(2-fluorophenyl)carbonyl-2-(4-iodomethylphenyl)-3,3-diphenylpropylamine.
• N-(4-fluorophenyl)carbonyl-2-(4-iodomethylphenyl)-3,3-diphenylpropylamine.
• N-(4-trifluoromethylphenyl)carbonyl-2-(4-iodomethylphenyl)-3,3-diphenylpropylamine.
• N-(3,5-bistrifluoromethylphenyl)carbonyl-2-(4-iodomethylphenyl)-3,3-diphenylpropylamine.
• N-(2-thiophene) carbonyl-2-(4-iodomethylphenyl)-3,3-diphenylpropylamine.
• N-(5-methyl-2thiophene)carbonyl-2-(4-iodomethylphenyl)-3,3-diphenylpropylamine.
• N-(4-chlorophenyl)carbonyl-2-(3,4-methylenedioxyphenyl)-3,3-diphenylpropylamine.
• N-(2-propyl) carbonyl-1,2,2-triphenylcyclopropylmethylamine.

The compounds of this invention may also include the respective hydrates of compounds specifically identified herein.

The compounds of formula I may be prepared according to the following reaction schemes.

Reaction Scheme 1 displays a method of making the compounds of formula I, where R¹–R⁵, W, X, Y and Z are as defined above. Treatment of a suitable substituted or unsubstituted diphenyl methyl-, fluorenyl-, or 10,11-dihydro-5H-dibenzo[1,d]cydohepten-4-yl chloride or bromide with an aryl- or heteroaryl acetonitrile using n-BuLi and the like or phase-transfer conditions, afford nitrile intermediates of structure k Reduction of A with LAH, NaBH₄/BH₃ and the like leads to the formation of amines C. Treatment of structure A with methylene chloride in the presence of potassium amide/liquid ammonia leads to the formation of structure B. Reduction of the nitrile group of structure B with LAH, NaBH₄/BH₃ and the like leads to an amine of structure D. By rewrng C or D with acid chlorides as set forth below in Scheme I in combination with bases such as NaOAc and the like, organic acids in combination with activating agents such as 1,1′-carbonyldiimidazole and the like, sulfonyl chlorides, chloroformates, isocyanates, isothiocyanates, or a suitable organic sulfonyl chloride, compounds of structure I are obtained. Optionally, nitrites of structure A, when treated with diisobutylaluminum hydride (DiBAL), are converted to aldehydes of structure E. Treatment of E with Rink resin affords resin-bound imines of structure F which are reduced with sodium triacetoxy borane to resin-bound imines of structure G. Treatment of G with an appropriate acid in the presence of O-(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (hereinafter referred to as “HATU”) and diisopropylethylamine (DIEA) affords compounds of structure I. Compounds of structure I may also be prepared by the reaction of amines of structure H with appropriate carboxylic acids in the presence of resin-bound 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide which is prepared from 1-(3dimethylaminopropyl)-3-ethylcarbodiimide and Merrifield resin.

To prepare the pharmaceutical compositions of this invention, one or more compounds or salts thereof of the invention, as the active ingredient, is intimately admixed with a pharmaceutical carrier according to conventional pharmaceutical compounding techniques, which carrier may take a wide variety of forms depending on the form of preparation desired for administration, e.g., oral or parenteral. In preparing the compositions in oral dosage form, any of the usual pharmaceutical media may be employed. Thus for liquid oral preparations, such as for example, suspensions, elixirs and solutions, suitable carriers and additives include water, glycols, oils, alcohols, flavoring agents, preservatives, coloring agents and the like; for solid oral preparations, such as, for example, powders, capsules and tablets, suitable carriers and additives include starches, sugars, diluents, granulating agents, lubricants, binders, disintegrating agents and the like. Because of their ease in administration, tablets and capsules represent the most advantageous oral dosage form, in which case solid pharmaceutical carriers are obviously employed. If desired, tablets may be sugar coated or enteric coated by standard techniques. For parenterals, the carrier will usually comprise sterile water, though other ingredients, for example, for purposes such as aiding solubility or for preservation, may be included. Injectable suspensions may also be prepared, in which case appropriate liquid carriers, suspending ats and Fte ike may be employed. The pharmaceutical compositions herein will preferably contain per dosage unit, e.g., tablet, capsule, powder, injection, teaspoonful and the like, from about 50 to about 100 mg of the active ingredient, although other unit dosages may be employed. The compounds of this invention may also be applied or utilized topically. If the delivery parameters of the topically active pharmaceutical or cosmetic agent so require, the topically active composition of this invention may preferably be further composed of a pharmaceutically or cosmetically acceptable vehicle capable of functioning as a delivery system to enable the penetration of the topically active agent into the skin. In alternative embodiments, the topically active pharmaceutical or cosmetic composition may be optionally combined with other ingredients such as moisturizers, foaming agents, cosmetic adjuvants, anti-oxidants, surfactants, foaming agents, conditioners, humectants, fragrances, viscosifiers, buffering agents, preservatives, and the like in an amount which will not destroy the active ingredient in order to produce cosmetic or pharmaceutical products.

The topically active pharmaceutical or cosmetic composition should be applied in an amount effective to treat inflammation of mammalian skin. As used herein “amount effective” shall mean an amount sufficient to ameliorate inflammation of mammalian skin. A composition containing 0.001–10.0% of active agent is applied to the skin surface when amelioration of an inflammatory condition is desired. Preferably, a composition containing 0.05–5.0% of active agent is applied to the skin surface such that, based

TABLE 1
Physical and Biological Properties of Triphenylpropylamine and Triphenylcyclopropyl amine Derivatives

										hPR
									hGR	% inh
cmp	R1	R2	R3	R4	X	Y	Z	mp, ° C.	IC50 (nM)	10 μM
1	H	Ph	H	PhCH2	H, H	H, H	CO	146.0–147.0	890	−0.2
2	H	Ph	H	2-CIPhCH2	H, H	H, H	CO	140.5–141.2	134	−23
3	H	Ph	H	4-CIPhCH2	H, H	H, H	CO	168.4–170.9	480	4
4	H	Ph	H	4-MePhCH2	H, H	H, H	CO	142.3–143.6	528	12
5	H	Ph	H	2-MeOPhCH2	H, H	H, H	CO	156.9–158.9	62%
6	H	Ph	H	4-MeOPhCH2	H, H	H, H	CO	157–159	910
7	H	Ph	H	3,4-MeOPhCH	H, H	H, H	CO	123–124.5	910	11.6
8	H	Ph	H	2,6-diCIPhCH2	H, H	H, H	CO	165.2–166.5	340	3
9	H	Ph	H	3,4-dICIPhCH2	H, H	H, H	CO	65–68	1480
10	H	Ph	H	2-CF3PhCH2	H, H	H, H	CO	109–111.5	780	15
11	H	Ph	H	3-CF3PhCH2	H, H	H, H	CO	106.8–111.3	830	20
12	H	Ph	H	4-CF3PhCH2	H, H	H, H	CO	119.5–120.3	1500	15
13	H	Ph	H	Ph2CH	H, H	H, H	CO	178.7–179.8	780
14	H	4-CIPh	H	PhCH2	H, H	H, H	CO	151.5–152.7	72	18
15	4-F	Ph	H	PhCH2	H, H	H, H	CO	87.5–89.7	21
16	4-F	Ph	H	2-CIPhCH2	H, H	H, H	CO	127.3–129.4	45
17	4-F	Ph	Me	PhCH2	H, H	H, H	CO	86.9–88.2
18	H	Ph	H	Ph	H, H	H, H	CO	161.5–163	610	14.1
19	H	Ph	H	Ph(CH2)2	H, H	H, H	CO	107.4–109.0	141	24
20	H	Ph	H	2-MeOPh(CH2)2	H, H	H, H	CO	137–140	58	9
21	H	4-CIPh	H	2-MeOPh(CH2)2	H, H	H, H	CO	122.2–123.5	57	21
22	H	Ph	H	2-CIPh(CH2)2	H, H	H, H	CO	135.0–135.8	103
23	4-F	Ph	H	2-MeOPh(CH2)2	H, H	H, H	CO	78.9–80.9	22
24	H	Ph	H	Ph(CH2)3	H, H	H, H	CO	78.1–81.0	670	10
25	H	Ph	H	PhCH2	H, H	H, H	SO2	172.9–174.2	210
26	H	Ph	H	4-MePh	H, H	H, H	SO2	139.7–142.1	175
27	H	Ph	H	PhSO2CH2	H,H	H, H	CO	188.9–187.5	67
28	H	Ph	H	4-MePhSO2CH2	H,H	H, H	CO	190.3–191.9	57
29	H	Ph	H	2-thiopheneCH2	H, H	H, H	CO	130–132	8	28.3
(+)			(+)				24
(−)			(−)				>800
30	H	Ph	H	5-Me-2-thiophene	H, H	H, H	CO	183.5–185	50
31	4-F	Ph	H	2-thiopheneCH2	H, H	H, H	CO	84.9–85.3	8
32	4-F	Ph	H	5-Me-2-thiopheneCH2	H, H	H, H	CO	127.9–128.9	7
33	H	4-IPh	H	2-thiopheneCH2	H, H	H, H	CO	127–130	8.6
34	H	4-CIPh	H	2-thiopheneCH2	H, H	H, H	CO	126.3–127.0	21	17
35	H	4-CIPh	H	3-thiopheneCH2	H, H	H, H	CO	128.4–127.9	54
36	H	Ph	H	3-thiopheneCH2	H, H	H, H	CO	135–138	25	22
37	H	Ph	H	2-thiophene(CH2)3	H, H	H, H	CO	105.5–108.9	500	4
38	H	Ph	H	2-thiopheneCH═CH(t)	H, H	H, H	CO	217.3–218.9	189
39	H	Ph	H	3-thiopheneCH═CH	H, H	H, H	CO	204.8–206.5	727
40	H	Ph	H	2-thiophene	H, H	H, H	SO2	169.1–170.9	151	22
41	H	4-CIPh	H	2-thiophene	H, H	H, H	SO2	180.4–181.9	491
42	H	Ph	H	3-thiophene	H, H	H, H	CO	153.5–154.7	68	18
43	H	Ph	H	2-benzothiophene	H, H	H, H	CO	218.3–218.8	495
44	H	Ph	Me	2-thiopheneCH2	H, H	H, H	CO	107–109.3	133
45	H	Ph	H	2-thiophene	H, H	H, H	CO	139–142	31	5
46	H	2-thio	H	2-thiopheneCH2	H, H	H, H	CO	138.2–139.9	723
47	H	Ph	H	3-indoleCH2	H, H	H, H	CO	89–93	416	17
48	H	Ph	H	3-indole(CH2)2	H, H	H, H	CO	100–114	605	19
49	H	Ph	H	2-pyridylCH2	H, H	H, H	CO	120.1–121.7	200	11
50	H	Ph	H	NHPh	H, H	H, H	CO	205–206
51	H	Ph	H	2-MeOPhNH	H, H	H, H	CO	203–204	32%
52	H	Ph	H	2-CIPhNH	H, H	H, H	CO	210–211	273
53	H	Ph	H	2-FPhNH	H, H	H, H	CO	190–191	293
54	H	Ph	H	PhCH2NH	H, H	H, H	CO	170–171	219
55	H	Ph	H	2,4-diCIPhCH2NH	H, H	H, H	CO	166–167	121
56	H	Ph	H	PhO	H, H	H, H	CO	128–129	310
57	H	Ph	H	4-CIPhO	H, H	H, H	CO	159–160	294
58	H	Ph	H	4-FPhO	H, H	H, H	CO	150–151	240
59	H	Ph	H	2-NapthO	H, H	H, H	CO	151–152	155
60	H	Ph	H	Pr	H, H	H, H	CO	88–89	446
61	H	Ph	H	i-Pr	H, H	H, H	CO	114–115	584
62	H	Ph	H	n-Bu	H, H	H, H	CO	78–79	121
63	H	Ph	H	i-Bu	H, H	H, H	CO	112–113	316
64	H	Ph	H	t-Bu	H, H	H, H	CO	143–144	296
65	H	Ph	H	CH2CO2Et	H, H	H, H	CO	103–105.5	937
66	H	Ph	H	PhCH2	SB	H, H	CO	148.7–150.8	888	18
67	H	Ph	H	2-MeOPhCH2	SB	H, H	CO	159.4–161.1	23%
68	H	Ph	H	2-CIPhCH2	SB	H, H	CO	162.4–184.2	46%
69	H	Ph	H	2-CF3PhCH2	SB	H, H	CO	153.9–155	15%
70	H	Ph	H	2-MeOPh(CH2)2	SB	H, H	CO	173.5–175.8	53%
71	H	Ph	H	2-thiopheneCH2	SB	H, H	CO	128.7–130.5	820	16
72	H	Ph	H	5-Me-2-thiophene	SB	H, H	CO	158.3–160.5	33%
73	H	Ph	H	PhCH2	(CH2)2	H, H	CO	172.7–174.8	770
74	H	Ph	H	2-MeOPh(CH2)2	(CH2)2	H, H	CO	134.3–136.8	388
75	H	Ph	H	2-thiopheneCH2	(CH2)2	H, H	CO	175–177.5	363
76	H	Ph	H	3-thiopheneCH2	(CH2)2	H, H	CO	167.3–169.3	571
77	H	Ph	H	5-Me-2-thiophene	(CH2)2	H, H	CO	172.1–173	882
78	H	Ph	H	PhCH2	H, H	CH2	CO	150–152	1200	6
79	H	Ph	H	3,4-MeOPhCH2	H, H	CH2	CO	131–133.5	1000	24.5
80	H	Ph	H	2-CIPhCH2	H, H	CH2	CO	128.5–130.5	955	−11
81	H	Ph	H	2-MeOPh(CH2)2	H, H	CH2	CO	187.5–189	709
82	H	Ph	H	CHPh2	H, H	CH2	CO	166–169	510	−20.4
83	H	Ph	H	n-propyl	H, H	CH2	CO	149–150	573	45
84	H	Ph	H	i-propyl	H, H	CH2	CO	187–168	612	15.3
85	H	Ph	H	2-Me-propyl	H, H	CH2	CO	142–143	68%	7.2s
86	H	Ph	H	t-butyl	H, H	CH2	CO	121–122	665	12.6
87	H	Ph	H	n-butyl	H, H	CH2	CO	122–123	681	19.8
88	H	Ph	H	2-thiopheneCH2	H, H	CH2	CO	135–137	425
89	H	Ph	H	3-thiopheneCH2	H, H	CH2	CO	130–135	570	22
90	H	Ph	H	2-thiophene	H, H	CH2	CO	152.5–155	612
91	H	Ph	H	5-Me-2-thiophene	H, H	CH2	CO	168–170.5	421
92	H	Ph	H	PhNH	H, H	CH2	CO	209–210	1488	−1
93	H	Ph	H	2-FPhNH	H, H	CH2	CO	235–230	17%	33.9
94	H	Ph	H	2-MeOPhNH	H, H	CH2	CO	246–247	13%	−18.6
95	H	Ph	H	PhCH2NH	H, H	CH2	CO	231–232	4%	−14.3
96	H	Ph	H	PhO	H, H	CH2	CO	146–147	927	9.9
97	H	Ph	H	4-CIPhO	H, H	CH2	CO	171–172	157	12.5
									Molecular	%
Cmpd	R1	R2	R3	R4	X	Y	Z	Mass	Ion MOCH	Inhibition
98	H	3,4-(OCH2O)Ph	H	4-CIPhCH2	H, H	H, H	CO	484.0	486
99	H	3,4-(OCH2O)Ph	H	2-thiopheneCH2	H, H	H, H	CO	455.8	458	35
100	H	3,4-(OCH2O)Ph	H	3-Me-5-CI-benzo-	H, H	H, H	CO	554.1	554, 558	18
				thiophene-2-CH2
101	H	3,4-(OCH2O)Ph	H	5-CI-benzo-	H, H	H, H	CO	540.1	540, 542	26
				thiophene-2-CH2
102	H	3,4-(OCH2O)Ph	H	2-pyridineCH2	H, H	H, H	CO	450.5	451	51
103	H	3,4.(OCH2O)Ph	H	3-CF3phenylCH2	H, H	H, H	CO	517.5	518	37
104	H	3,4-(OCH2O)Ph	H	3,5-di-CF3phenylCH2	H, H	H, H	CO	585.5	588	52
105	H	3,4-(OCH2O)Ph	H	4-NO2phenylCH2	H, H	H, H	CO	494.5	495	24
106	H	3,4-(OCH2O)Ph	H	4-BuOphenylCH2	H, H	H, H	CO	521.7	522	52
107	H	3,4-(OCH2O)Ph	H	2-MeOphenylCH2	H, H	H, H	CO	479.6	480	28
108	H	3,4-(OCH2O)Ph	H	3,5-di-MeOphenylCH2	H, H	H, H	CO	509.6	510	38
109	H	3,4-(OCH2O)Ph	H	phenylCH2	H, H	H, H	CO	449.5	450	22
110	H	3,4-(OCH2O)Ph	H	3-FphenylCH2	H, H	H, H	CO	487.5	468	20
111	H	3,4-(OCH2O)Ph	H	2,4-diF-phenylCH2	H, H	H, H	CO	485.5	488	80
112	H	3,4-(OCH2O)Ph	H	2,4-di-Cl-phenylCH2	H, H	H, H	CO	518.4	518, 520	36
113	H	3,4-(OCH2O)Ph	H	3,4-diCl-phenylCH2	H, H	H, H	CO	518.4	518, 520	31
114	H	3,4-(OCH2O)Ph	H	phenylthioCH2	H, H	H, H	CO	481.6	482	41
115	H	3,4-(OCH2O)Ph	H	3-thiophene	H, H	H, H	CO	441.5	442	28
116	H	3,4-(OCH2O)Ph	H	2-thiophene	H, H	H, H	CO	441.5	442	62
117	H	3,4-(OCH2O)Ph	H	phenyl	H, H	H, H	CO	435.5	438	28
118	H	3,4-(OCH2O)Ph	H	2-MeO-phenyl	H, H	H, H	CO	485.5	488	38
119	H	3,4-(OCH2)Ph	H	2-indole	H, H	H, H	CO	476.6	475	31
120	H	3,4-(OCH2)Ph	H	3,5-dl-CF3phenyl	H, H	H, H	CO	571.5	572	27
121	H	3,4-(OCH2)Ph	H	3-NO2-phenyl	H, H	H, H	CO	480.5	481	10
122	H	3,4-(OCH2)Ph	H	3-NO2-4-Me-phenyl	H, H	H, H	CO	494.5	495	33
123	H	3,4-(OCH2)Ph	H	3-CN-phenyl	H, H	H, H	CO	460.5	461	51
124	H	3,4-(OCH2)Ph	H	phenylethyl	H, H	H, H	CO	463.6	464	35
125	H	3,4-(OCH2)Ph	H	4-1Bu-phenyl	H, H	H, H	CO	491.6	492	31
126	H	3,4-(OCH2)Ph	H	4-Me-phenyl	H, H	H, H	CO	449.5	450	46
127	H	3,4-(OCH2)Ph	H	2,4-dlF-phenyl	H, H	H, H	CO	471.5	472	61
128	H	3,4-(OCH2)Ph	H	4-F-phenyl	H, H	H, H	CO	453.5	454	54
129	H	3,4-(OCH2)Ph	H	2-Cl-phenyl	H, H	H, H	CO	470.0	470, 472	41
130	H	3,4-(OCH2)Ph	H	4-Cl-phenyl	H, H	H, H	CO	470.0	470, 472	37
131	H	3,4-(OCH2)Ph	H	3,5-diCl-phenyl	H, H	H, H	CO	504.4	504, 506	18
132	H	3,4-(OCH2)Ph	H	4,5-diCl-phenyl	H, H	H, H	CO	504.4	504, 506	69
133	H	3,4-(OCH2)Ph	H	2-Me-phenyl	H, H	H, H	CO	449.5	450	46
134	H	3,4-(OCH2)Ph	H	4-biphenylCH2	H, H	H, H	CO	525.6	526	29
135	H	4-CF3-Ph	H	2-thiopheneCH2	H, H	H, H	CO	479.6	480	31
136	H	4-CF3-Ph	H	2-thiophene	H, H	H, H	CO	465.5	466	38
137	H	4-CF3-Ph	H	2-Cl-phenyl	H, H	H, H	CO	494	494, 496	45
138	H	4-CF3-Ph	H	3,4-diCl-phenylCH2	H, H	H, H	CO	542.4	542, 544	33
139	H	4-CF3-Ph	H	2,4-diCl-phenyl	H, H	H, H	CO	528.4	528, 530	42
140	H	4-CF3-Ph	H	3-Me-phenylCH2	H, H	H, H	CO	487.6	488	57
141	H	4-CF3-Ph	H	phenylCH2	H, H	H, H	CO	473.5	474	66
142	H	4-CF3-Ph	H	2-pyridineCH2	H, H	H, H	CO	474.5	475	39
143	H	4-CF3-Ph	H	4-MeS-phenylCH2	H, H	H, H	CO	519.6	520	19
144	H	4-CF3-Ph	H	2-MeO-4-Cl-phenyl	H, H	H, H	CO	524	524, 526	33
145	H	4-CF3-Ph	H	5-Cl-benzo-	H, H	H, H	CO	564.1	564, 565	54
				thiophene-2-CH2
146	H	4-CF3-Ph	H	2-Cl-phenylCH2 H, H	H, H	CO	508.0	508.2	39
147	H	4-CF3-Ph	H	2,4-diF-phenylCH2	H, H	H, H	CO	509.5	510.2	55
148	H	4-CF3-Ph	H	2-MeO-phenylCH2	H, H	H, H	CO	503.6	504	42
149	H	4-CF3-Ph	H	3,5-diMeO-phenylCH2	H, H	H, H	CO	533.6	534	42
150	H	4-CF3-Ph	H	4-CF2-phenylCH2	H, H	H, H	CO	541.5	542	61
151	H	4-CF3-Ph	H	3,5-diCF3-phenylCH2	H, H	H, H	CO	609.5	610	41
152	H	4-CF3-Ph	H	4-Me-phenylCH2	H, H	H, H	CO	487.6	488	41
153	H	4-CF3-Ph	H	Ph2CH	H, H	H, H	CO	549.6	550	69
154	H	4-CF3-Ph	H	4-NO2-phenylCH2	H, H	H, H	CO	518.5	519	34
155	H	4-CF3-Ph	H	4-(Me2N)-phenylCH2	H, H	H, H	CO	516.6	517	29
156	H	4-CF3-Ph	H	4-biphenylCH2	H, H	H, H	CO	549.6	550	19
157	H	4-CF3-Ph	H	2-naphthylCH2	H, H	H, H	CO	523.6	524	10
158	H	4-CF3-Ph	H	5-Cl-3-Me-benzo-	H, H	H, H	CO	578.1	578, 580	16
				thiopheneCH2
159	H	4-CF3-Ph	H	4-(Me2N)-phenyl(CH)2	H, H	H, H	CO	526.6	529	12
160	H	4-CF3-Ph	H	3,5-diCF3-phenyl	H, H	H, H	CO	595,5	596	10
161	H	4-I-Ph	H	2-Cl-phenylCH2	H, H	H, H	CO	565.9	566, 568	42
162	H	4-I-Ph	H	4-Cl-phenylCH2	H, H	H, H	CO	565.9	566, 568	30
163	H	4-I-Ph	H	3,4-diCl-phenylCH2	H, H	H, H	CO	600.3	600	44
164	H	4-I-Ph	H	2-F-phenylCH2	H, H	H, H	CO	549.4	550	40
165	H	4-I-Ph	H	4-F-phenylCH2	H, H	H, H	CO	549.4	550	79
166	H	4-I-Ph	H	4-CF2-phenylCH2	H, H	H, H	CO	599.4	600	46
167	H	4-I-Ph	H	3,5-diCF33-phenylCH2	H, H	H, H	CO	667.4	668	63
168	H	4-I-Ph	H	2-MeO-phenylCH2	H, H	H, H	CO	561.5	562	32
169	H	4-I-Ph	H	3-MeO-phenylCH2	H, H	H, H	CO	561.5	562	45
170	H	4-I-Ph	H	4-MeO-phenylCH2	H, H	H, H	CO	561.5	562	25
171	H	4-I-Ph	H	3,5-diMeO-phenylCH2	H, H	H, H	CO	591.5	592	25
172	H	4-I-Ph	H	2-Cl-phenyl	H, H	H, H	CO	551.9	552	32
173	H	4-I-Ph	H	4-Cl-phenyl	H, H	H, H	CO	551.9	552	72
174	H	4-I-Ph	H	3,4-diCl-phenyl	H, H	H, H	CO	586.3	587	50
175	H	4-I-Ph	H	2-F-phenyl	H, H	H, H	CO	535.4	536	65
176	H	4-I-Ph	H	4-F-phenyl	H, H	H, H	CO	535.4	536	68
177	H	4-I-Ph	H	4-CF3-phenyl	H, H	H, H	CO	585.4	586	53
178	H	4-I-Ph	H	3,5-diCF3-phenyl	H, H	H, H	CO	653.4	654	53
179	H	4-I-Ph	H	2-thiophene	H, H	H, H	CO	523.4	524	53
180	H	4-I-Ph	H	5-Me-2-thiophene	H, H	H, H	CO	537.5	538	57
181	H	4-I-Ph	H	2-MeO-phenyl	H, H	H, H	CO	547.4	548	41
182	H	4-I-Ph	H	3-MeO-phenyl	H, H	H, H	CO	547.4	548	15
183	H	4-I-Ph	H	3,5-diMeO-phenyl	H, H	H, H	CO	577.5	578	42

upon a square cm of skin surface, from about 2 μl/cm² to about 8 μl/cm² of topically active agent is present when amelioration of an inflammatory condition is desired.

The following examples are merely illustrative of the compounds, methods of making said compounds, compositions and methods of using said compounds and compositions, and do not serve to limit the scope of this invention.

EXAMPLE 1

2,3,3-Triphenylpropionitrile, (Hauser, C. R. et al., Formation and Preferential β-Alkylation of the Dicarbanion of 2,3,3-Triphenylpropionitrile by Means of Potassium Amide in Liquid Ammonia. J. Amer. Chem. Soc., 1959, 81, 4099A102) was made as follows. A solution of phenylacetonitrile (1.00 g, 0.0086 mol) and THF (17 mL) was cooled to −78° C. in a dry iceacetone bath and treated dropwise with a solution of nbutyllithium in hexane (3.80 mL, 0.0095 mol). After stirring for 45 minutes at −78° C., a solution of diphenyl methylchloride (1.75 g, 0.0086 mol) and THF was added dropwis to give a light yellow solution. After stirring at room temperature overnight, water (20 mL) and diethyl ether (50 mL) were added with vigorous stirring. The organic layer was separated, dried over anhydrous magnesium sulfate (MgSO₄), filtered, and evaporated to give an oil. This material was triturated and filtered to give 1,2,2-triphenylpropionitrile.

EXAMPLE 2

9H-(Fluoren-9-yl)phenylacetonitrile was prepared using the same procedure as that described in Example 1, however, 9bromofluorene was substituted for diphenylmethylchloride. 9H(Fluoren-9-yl)phenylacetonitrile was obtained, having a melting point of 146–148.3° C.

EXAMPLE 3

(10,11-Dihydro-5H-dibenzo[1,d]cyclohepten-4-yl)phenylacetonitrile was made using the same procedure as described above in Example 1, with the exception that 5-chloro-10,11-dihydro-5-H-dibenzo[a,d]cydoheptene was substituted for diphenylmethyichloride. (10,11-Dihydro-5-H-dibenzo[1,d]cyclohepten-4-yl)phenylaetonitrile was obtained, having a melting point of 134.1–147.7° C.

EXAMPLE 4

2-(4-Chlorophenyl)-3,3diphenylpropionitrile was made using the same procedure as described for Example 1, but substituting 4-chlorophenylacetonitrile for phenylacetonitrile. The compound obtained had a melting point of 115.1–115.6° C.

EXAMPLE 5

2-(2-Thienyl)-3,3-diphenylpropionitrile was made using the following procedure. To a mixture of 2-thiophenacetonitrile (16.30 g, 0.081 mol), benzyltriethylammonium chloride (0.185 g, 0.900081 mol), and 50% sodium hydroxide, diphenylmethylchloride (10.00 g, 0.081 mol) was added dropwise. this mixture was stirred for two hours at room temperature, heated at 40° C. for 30 minutes and then was treated with benzaldehyde (0.18 g, 0.0017 mol). The reaction mixture was poured into an icewater mixture (200 ml) and extracted twice with dichloromethane. The organic layers were combined, washed with 2N hydrochloric acid (100 ml), water (100 ml), and saturated sodium chloride solution (100 ml), dried over magnesium sulfate, filtered and evaporated. The residue was chromatographed on flash silica to give a solid which was recrystallized three times from ethanol affording 17.45 g (74.3%) of 2-(2-Thienyl)-3,3-diphenylpropionitrile as a crystalline solid, having a melting point of 102.7–105.3° C.

EXAMPLE 6

3,3-Bis-(4-fluorophenyl)-2-phenylpropionitrile was made using the same procedure as described in Example 5 but substituting phenylacetonitrile for 2-thiopheneacetonitrile and chlorobis(4-fluorophenyl)methane for diphenylmethylchloride. The end product had a melting point of 142.5–143.8° C.

EXAMPLE 7

2-(4-lodophenyl)-3,3-diphenylpropionitrile was made using the same procedure as described in Example 5, but substituting 4-iodophenylacetonitrile for 2-thiopheneacetonitrile.

EXAMPLE 8

1,2,2-Triphenylcyclopropyinitrile was made using the procedure of C. R. Hauser, T. M. Harris, and T. G. Ledford [J. Amer. Chem. Soc., 1959, 81, 4099–4102]. A solution of KNH₂ and liquid NH₃ was made by adding potassium (24.5 G, 0.63 mol) to liquid NH₃ (1500 ml). 2,3,3-triphenylpropionitrile (87.5 g, 0.31 mol) was slowly added to the KNH₂/NH₃ solution. After stirring for 10 minutes, this mixture was treated with a solution of dichloromethane (31.5 g, 0.37 mol) and diethyl ether (150 ml). After 1.5 hour, another portion of dichloromethane (6.0 g, 0.071 mol) and diethyl ether (25.0 ml) was added and the reaction mixture stirred for another hour at −78° C. Diethyl ether was added and the NH₃ was allowed to evaporate. The ethereal solution was washed with water, 2N hydrochloric acid and water. The organic layer was separated, dried over potassium carbonate, filtered and evaporated to a solid residue. This material was recrystallized twice from methanol affording 47.0 g (51%) of 1,2,2-Triphenylcyclopropyinitrile as a crystalline solid.

EXAMPLE 9

2,3,3-Triphenylpropylamine was made according to the following procedure. A solution of 2,3,3-triphenylpropionitrile (10.00 g, 0.035 mol) and THF (80 ml) was added dropwise to a solution of LiAIH₄ (3.40 g, 0.089 mol) in THF (100 ml) at 0° C. The resulting mixture was stirred for 24 hours at room temperature and then refluxed for 24 hours. After cooling in an ice bath, the reaction mixture was treated with water (3.40 ml), 3N sodium hydroxide (10.20 ml) and water (3.4 ml) followed by the addition of magnesium sulfate. The mixture was filtered and the filtrate was evaporated to an oil. This material was dissolved in diethyl ether (30 ml) and diethyl ether/anhydrous hydrochloric acid (25 ml, 0.025 mol) was added. A white solid was filtered and partitioned between diethyl ether and 3N sodium hydroxide. The organic layer was separated, dried over potassium carbonate, filtered, and evaporated affording 2,3,3-Triphenylpropylamine as a crystalline solid.

EXAMPLE 10

2-(4-Chlorophenyl)-3,3-diphenylpropylamine was made using the same procedure as described in Example 9, but substituting 2-4-Chlorophenyl)-3,3-diphenylpropionitrile for 2,3,3-triphenylpropionitrile. The end product had a melting point of 104.1–105.7° C.

EXAMPLE 11

2-(9H-[Fluoren-9-yl])-2-(phenyl)ethylamine was made using the procedure as set forth in Example 9, but substituting 9H-(Fluoren-9-yl)phenylacetonitril for 2,3,3-triphenylpropionitrile and diethyl ether for THF. An oil was obtained.

EXAMPLE 12

3,3-Bis-(4-fuorophenyl)-2-(phenyl)propylamine was made using the procedure as set forth in Example 9, but substituting 3,3bis-(4-fluorophenyl)-2-phenylpropionitrile for 2,3,3triphenylpropionitrile and diethyl ether for THF. The endproduct was a white solid.

EXAMPLE 13

3,3-Diphenyl-2-(2-thienyl)propylamine was made using the procedure as set forth in Example 9, but substituting 2-(2-Thienyl)-3,3-diphenylprionitrile for 2,3,3-triphenylpropionitrile and diethyl ether for THF. The end product was a beige solid having a melting point greater than 200° C. (decomposition).

EXAMPLE 14

1,2,2-triphenylcydopropylmethylamine was made using the procedure as set forth in Example 9, but substituting 1,2,2-Triphenylcyclopropyinitrile for 2,3,3-triphenylpropionitrile and diethyl ether for THF. The end product was a white solid.

EXAMPLE 15

2-(4-lodophenyl)-3,3-diphenylpropylamine was made using the following procedure. A solution of TFA (3.30 g, 0.030 mol) and THF (10 ml) was slowly added to a slurry of sodium borohydrate (1.10 g, 0.029 mol) and THF (20 ml) at room temperature. After gas evolution ceased, the reaction was stirred for fifteen minutes and then treated dropwise with a solution of 2-(4-lodophenyl)-3,3-diphenylpropionitrile (4.87 g, 0.012 mol) and THF (20 ml). After stirring overnight at room temperature, water was added slowly followed by dichloromethane (40 ml). The organic layer was dried over potassium carbonate, filtered and evaporated to an oil. This material was dissolved in diethyl ether and treated with anhydrous hydrochloric acididiethyl ether (10 ml). A white solid was filtered and partitioned between dichloromethane and 3N sodium hydroxide. The organic layer was separated, dried over potassium carbonate, filtered and evaporated to give 2-(4-lodophenyl)-3,3diphenylpropylamine as a solid.

EXAMPLE 16

2-(10,11-Dihydro-5H-dibenzo[1,D]cyclohepten-4-yl)-2-(phenyl)ethylamine was made as follows. A solution of 4M BH₃-THF (24 ml, 0.024 mol) at room temperature was treated with a solution of (10,11-Dihydro-5H-dibenzo[1,d]cycloheptenyl)phenylacetonitrile (5.0 g, 0.016 mol) and THF (70 ml). The resulting solution was refluxed for 2 hours, cooled to 0° C. and treated with methanol (50 ml) followed by 6N hydrochloric acid (125 ml). The mixture was heated at 70° C. for 1 hour, cooled to 0° C., adjusted to pH 12 with 50% sodium hydroxide solution, and extracted two times with ethylacetate. The organic layers were combined, dried, filtered, and evaporated to a yellow oil. This material was triturated with hexane and filtered. The filtrate was evaporated and the residue was chromatographed on flash silica using ethylacetate:hexane (8:2) as the eluant to give a 2.29 g (46%) yield of 2-(10,11-Dihydro-5H-dibenzo[1,d]cyclohepten-4-yl)-2-(phenyl)ethylamine as an oil.

EXAMPLE 17

Compound 29 was made in accordance with the following procedure. A solution of thiopheneacetyl chloride (0.281 g, 0.0017 mol) and ethylene dichloride (8.0 ml) was added slowly to an iceooled mixture of 2,3,3-Triphenylpropylamine (0.50 g, 0.0017 mol), sodium acetate (0.18 g, 0.0022 mol) and ethylene chloride (8.0 ml). After stirring overnight at room temperature, water was added with thorough mixing. The resulting organic layer was separated, washed successively with 1N sodium hydroxide solution and 1N hydrochloric acid solution dried over magnesium sulfate, filtered and evaporated to an oil which solidified. Two recrystallizations of this material afforded 0.410 g (59%) of 29 as a crystalline solid, having a melting point of 130–132° C.

EXAMPLE 18

Other compounds may be obtained in accordance with the procedure set forth in Example 17, requiring the substitution for thiopheneacetyl chloride or 2,3,3-Triphenylpropylamine, such as compounds: 1, 6, 7, 18, 29, 78, 79, and 82.

EXAMPLE 19

Compound 80 was made using the following procedure: A solution of 2-chlorphenylacetic acid (0.289 g, 0.0017 mol), 1,1′-carbonyidiimidazole (0.271 g, 0.0017 mol) and acetonitrile (25 ml) was stirred for twenty minutes at room temperature and treated with 1,2,2-triphenylcycdopropylmethylamine (0.500 g, 0.0017 mol). After stirring for 24 hours, the reaction was evaporated and the residue dissolved in methylene dichloride. This solution was washed with water (10 ml), 1N HCl (10 ml), and water (10 ml). The organic layer was separated, dried over magnesium sulfate, filtered, and evaporated to an oil. This material was dissolved in ethylene dichloride and diethyl ether was added causing a crystalline solid to form. Filtration afforded 0.501 g (65%) of 80 as a crystalline solid with a melting point of 128.5–130.5° C.

EXAMPLE 20

Following the procedure of Example 19, substituting for the 2-chlorophenylacetic acid or 1,2,2-triphenylcyclopropylmethylamine equivalent amounts of the appropriate starting materials and substituting ethylene dichloride for the acetonitrile used therein, the following compounds may be obtained: 2, 3, 4, 5, 8, 9, 10, 11, 12, 13, 14, 19, 20, 21, 22, 24, 25, 26, 27, 28, 30, 34, 37, 38, 39, 40, 41, 42, 43, 45, 46, 48, 49, 61, 62, 63, 64, 81, 83, 84, 85, 86, 87, 88, 89, and 90.

EXAMPLE 21

Compound 66 was made as follows. A solution of phenyl acetic acid (0.30 g, 0.0024 mol), 2-(9H-[Fluoren-9-yl])-2-(phenyl)ethylamine (0.70 g, 0.0024 mol), and ethylene dichloride (10 ml) was treated with 1-(3dimethylaminopropyl)-3-ethylcarbondiimide hydro mol). After stirring overnight, the reaction solution was washed with 3N sodium hydroxide, 6N HCl and saturated NaCl solution. The organic layer was separated, dried over magnesium sulfate and evaporated to a semi-solid. This material was triturated with diethyl ether and filtered to give a solid which was recrystallized from methanol affording 0.12 g (12%) of Compound 66 as a white crystalline solid having a melting point of 148.7–150.8° C.

EXAMPLE 22

Following the procedure of Example 21, substituting for the phenylacetic acid or 2-(9H-[Fluoren-9-yl])-2(phenyl)ethylamine equivalent amounts of the appropriate starting materials, the following compounds may be obtained: 15, 16, 17, 23, 31, 32, 44, 65, 67, 68, 69, 70, 71, 72, 74, 75, 76, 77, and 91.

EXAMPLE 23

Compound 52 was made in accordance with the following procedure: A solution of 2,3,3-Triphenylpropylamine (0.25 g, 0.0009 mol) and methylene dichloride (25 ml) was treated with 2-chlorophenyl isocyanate (0.13 g, 0.0009 mol) at room temperature. A solid formed which was filtered and recrystallized from methanol-hexane to give 0.14 g (75%) of 52 as a white crystalline solid having a melting point of 210–211° C.

EXAMPLE 24

Following the procedure of Example 23, substituting for the chlorophenyl isocyanate or 2,3,3-Triphenylpropylamine used therein, equivalent amounts of the appropriate starting materials, the following compounds may be obtained: 50, 51, 53, 54, 55, 92, 93, 94, and 95

EXAMPLE 25

Compound 40 was made as follows: An ice-cooled solution of 2,3,3-triphenylpropylamine (0.674 g, 0.0024 mol) and CHCl₃ (20 ml) was treated with 2-thiophenesulfonyl chloride (0.475 g, 0.0026 mol) followed by diisopropylethylamine (0.764 g, 0.0059 mol) and stiffed at room temperature overnight. The reaction was washed with 1N HCl (20 ml) and saturated NaCl solution. The organic layer was separated, dried over magnesium sulfate, filtered and evaprated affording 0.660 g (66%) of 40 as a solid having a melting point of 169–170.9° C.

EXAMPLE 26

Following the procedure of Example 25, substituting for the 2,3,3-Triphenylpropylamine used therein an equivalent amount of 2-(4chlorophenyl)-3,3-diphenylpropylamine, compound 41 may be obtained.

EXAMPLE 27

Compound 57 was made in accordance with the following procedure: To a solution of 2,3,3-Triphenylpropylamine (0.25 g, 00009 mol), triethylamine (0.09 g, 0.0009 mol) and CHCl₃ (25 ml) was added 4-fluorophenyl chloroformate (0.2 g, 0.0009 mol) and the resulting solution was stirred for 45 minutes. The reaction was then washed with 1N HCl, and brine. The organic layer was separated, dried over magnesium sulfate, filtered and evaporated to white solid. This material was recrystallized form methanol/hexane to give 0.15 g (39%) of 57 as a white crystalline solid having a melting point of 150–151° C.

EXAMPLE 28

Following the procedure of Example 27, but substituting for the 2,3,3-Triphenylpropylamine and 4-fluorophenyl chloroformate used therein, equivalent amounts of the appropriate starting materials, the following compounds may be obtained: 56, 58, 59, 96, and 97.

EXAMPLE 29

Compound 17 was made as follows: A mixture of N-[3,3bis4fluorophenyl)-2-phenylpropyl]-2-phenylacetamide [Compound 18] (0.84 g, 0.0019 mol) , dimethylsulfate (0.37 g, 0.0029 mol), benzyltriethylammonium chloride (0.14 g, 0.00075 mol), 50% NaOH (30 ml) was stiffed overnight at room temperature Water was added and the mixture was extracted with ethylene dichloride. The organic layer was separated, dried over potassium carbonate, filtered and evaporated to an oil which was crystallized from diethyl ether-hexane affording 0.080 g (9%) of 17 as a yellow crystalline solid having a melting point of 86.9–88.2° C.

EXAMPLE 30

Compound 98 was prepared as follows: A mixture of 2-(3,4-methylenedioxyphenyl)-3,3-diphenylpropylamine (18.0 g, 0.055 mol) and anhydrous THF (120 mL) at −70° C. was treated dropwise with a 1.0M solution of DiBAL (100 mL, 0.110 mol). The reaction was stirred for 1 hour at −70° C. and then at 25° C. for 1.5 hours. The reaction was cooled to 0° C. and treated with ethanol (20 mL) followed by 10% aqueous HCl (150 mL). Extraction with ethyl acetate, drying over anhydrous MgSO₄, evaporation and purification by flash chromatography (silica gel) afforded 2-(3,4-methylenedioxyphenyl)-3,3-diphenylpropionaldehyde a solid. A mixture of this material (8.0 g, 0.024 mol), Rink amine resin (8.73 g, 0.0044 mol), and trimethylorthotormate (60 mL) was shaken for 4 days, filtered and washed twice with trimethylorthoformate, metdylene chloride, and dichloroethane. The resulting resin was shaken with NaBH(Oac)₃ (4.63 g, 0.022 mol), acetic acid (1.83 mL) and dichloroethane (60 mL) for two days. The resulting resin was washed with methanol, methylene chloride, 10% acetic acidimethylene chloride, 10% triethylamine/methylene chloride, methylene chloride, and methanol. This resin (0.235 g, 0.0001 mol) was shaken for 2 days with HATU (0.090 g, 0.00024 mol), diisopropylethylamine, (175 μL), 4-chlorophenylacetic acid (0.085 g, 0.0005 mol), and DMF (2 mL). The resin was filtered and washed three times each with DMF, methylene chloride, and methanol and dried. The dried resin was treated with 10% TFA/methylene chloride and filtered. The filtrate was blown dry with nitrogen to afford 0.042 g (87%) of compound 98, electrospray mass spectrometry m/e=484.

EXAMPLE 31

Following the procedure of Example 30, but substituting for the 4-chlorophenylacetic acid and 2-(3,4-methylenedioxyphenyl)-3,3- diphenylpropylamine used therein, equivalent amounts of the appropriate starting materials, the following compounds may be obtained: 99–161, 164, 168,173, 174, 176–178,180, and 182.

EXAMPLE 32

Compound 162 was prepared as follows: A solution of 1-(3dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (7.67 g, 0.040 mol) and methylene chloride (300 mL) was washed with 10% NH₄OH, dried over MgSO₄, filtered and evaporated. The residue was dissolved in DMF (100 mL) and mixed with Merrifield resin (20.0 g, 0.020 mol) at 100° C. overnight. The mixture was filtered and the resin was washed with DMF, methanol, and methylene chloride. A mixture of this resin (0.48 g, 0.00048 mol), 4-chlorophenylacetic acid (0.0205 g, 0.00012 mol), 2(4-iodophenyl)-3,3 diphenylpropylamine (0.0413 g, 0.0001 mol), and CHCl₃ agitated for 2 days, filtered, and washed with CHCl₃. The filtrate was blown dry with nitrogen affording compound 163, 0.0425g. (88%), Cl mass spectrometry m/e=483.99.

EXAMPLE 33

Following the procedure of Example 32, but substituting for the 4chlorophenylacetic acid used therein, equivalent amounts of the appropriate starting materials, the following compounds may be obtained: 163, 165–167, 169–172, 175,179,181, and 183.

EXAMPLE 34

A human glucocorticoid receptor binding assay was carried out to determine the extent to which the compounds of this invention have the ability to bind to human glucocorticoid receptors. This binding ability may be indicative of the antiinflammatory activity of the compound. The test was carried out as follows.

Human glucocorticoid receptors were prepared from either insect cells (Sf21) infected with baculovirus hGR or from a lymphoblast cell line which expresses high levels of endogenous hGR (IM9). The receptor binding reactions, with or without test compounds, were set up in 96-well microtiter plates which were previously siliconized with SIGMACOTE™, a chlorinated organopolysiloxane in heptane. The binding components, 3(H) Triamcinolone acetonide (TAA), glycerol/molybdate-wntaining buffer and unlabeled compounds were added to the wells using a combination of BIOMEK laboratory automation system and repeat pipettes. After four hours of incubation, the samples were precipitated with polyethylene glycol and filtered through Whatman GF/F paper using a TOMTEK cell harvester. The filter mate with 96 samples were bound to a solidlphase scintillant and directly counted in a BETAPLATE counter. The IC₅₀ values were determined based on competition of ³H TAA with the test compounds at 6–8 concentrations ranging from 10^{−10–10−5} M and calculated using the Chung-Prusoff equation. The activity of test compounds to displace 3(H) TAA binding to hGR is also expressed as percent inhibition at 1 μM. The results of this test are set forth in Table 1 below.

EXAMPLE 35

A human progesterone receptor binding assay was performed in order to determine selectivity of the compounds, as follows. Human progesterone receptors were prepared from either insect cells (SF21) infected with baculovirus hPR A, or from a breast cancer cell line, T47D, which expresses high levels of endogenous hPR. The receptor binding reactions, with or without test compounds, were set up in 96-well microtiter plates which were previously siliconized with SIGMACOTE. The binding components, 3(H) R5020 Promegestone, a high affinity ligand for the progesterone receptors, glycerol/molybdatecontaining buffer and unlabeled compounds were added to the wells using a combination of BIOMEK laboratory automation system and repeat pipettes. After overnight incubation, the samples were precipitated with polyethylene glycol and filtered through Whatman GF/F paper using a TOMTEK cell harvester. The filter mate with 96 samples were bound to a solidphase scintillant and directly counted in the BETAPLATE counter. Only those compounds that were active in the human glucocorticoid receptor assay set forth in Example 30 were used for progesterone receptor binding to determine cross-reactivity profiles, if any. The activity of test compounds to displace 3(H) R5020 binding to hPR is expressed as percent inhibition at the two concentrations, 10⁻⁶ and 10⁻⁵ Molar. Those compounds that do not inhibit 3(H) TM binding by 50% at 10⁻⁵ M were not considered active. Surprisingly, the compounds of this invention selectively bind to the hGR but show little or no affinity for the hPR.

EXAMPLE 36

Several triphenylpropanamide compounds of this invention, having varying affinities for the human glucocorticoid receptor, were tested for topical antiinflammatory activity in mouse ear inflammation models. Compounds with low receptor affinity (IC₅₀>20 nM) were weakly active or inactive at reducing ear inflammation induced by the core sensitizer oxazolone. Compounds having receptor affinities closer to hyortsone were as nearly active as hydrocortisone in suppressing mouse oxazoloneinduced contact hypersensitization (MOCH) and phorbol ester-induced ear edema. The in vivo studies of this example were conducted as follows.

Albino male CD-1 mice, 7–9 weeks old were used in this example. A 0.005% (w/v) TPA or 20% (w/v) arachidonic acid (AA) solution was made in acetone. A 20 μl volume of the TPA or M was applied to the dorsal left ear of the mouse. Compounds of this invention were placed in a composition containing ethanol/propylene glycol at a ratio of 70:30 were applied to the left ear of each mouse in an amount of 20 μl immediately after application of the TPA or AA. The right ear was not treated. The mice were sacrificed by carbon dioxide inhalation 5.5 hours after administration of TPA and one hour after administration of AA, the left and right ears were removed and a 7 mm biopsy was removed from each ear and weighed. The difference in biopsy weights between the right and left ears was calculated. Antiinflammatory effects of compounds were evident as an inhibition of the increase in ear weight.

In determining the MOCH using the compounds of this invention, albino male CD-1 mice, 7–9 weeks old were induced on the shaved abdomen with 50 μl of 3% oxazolone in acetone/com oil (Day 0). On Day 5, a 20 μl volume of 2% oxazolone in acetone was applied to the dorsal left ear of the mouse. Compounds (made in ethanol/propylene glycol, 70:30) were applied to the left ear in 20 μl volume, one hour after oxazolone challenge.

The right ear was not treated. The mice were sacrificed by carbon dioxide inhalaton 24 hours after oxazolone challenge, the left and right ears were removed and a 7 mm biopsy was removed from each ear and weighed. The difference in biopsy weights between the right and left ears was calculated. Antiinflammatory effects of compounds were evident as an inhibition of the increase in ear weight.

The results of the foregoing in vivo testing is set fo in the following Table 2:

	TABLE 2
		Oxazolone Ear Swelling (MOCH)
	Compound No.	% inhibition vs. Vehicle at 1 mg

	2	4
	4	1
	5	13
	6	38
	9	18
	10	19
	11	33
	12	36
	13	10
	14	11
	15	47
	16	46
	19	2
	20	32
	22	15
	23	41
	24	21
	25	9
	26	−5
	27	20
	28	28
	29	83
	30	21
	31	14
	32	83
	33	74
	34	29
	35	36
	36	13
	37	25
	38	13
	39	24
	40	15
	41	3
	42	27
	43	47
	44	3
	45	31
	46	4
	47	51
	48	22
	49	20
	50	30
	53	24
	54	10
	55	18
	56	38
	57	13
	58	16
	60	27
	61	17
	62	36
	63	3
	64	26
	65	13
	66	20
	68	28
	69	43
	72	50
	74	18
	75	26
	76	23
	77	41
	79	18
	80	54
	81	22
	82	23
	83	−4
	84	54
	85	16
	87	22
	88	29
	89	16
	90	65
	91	13
	92	42
	93	26
	94	35
	95	16
	96	52
	97	50
	98	85

	hydrocortisone	75–85

In accordance with the foregoing table, for example, compounds 23, 15, and 16 had moderate topical activity whereas compounds 29, 32, and 98 were equiactive with hydrocortisone. Compounds 29 and 32 were tested for dose-related activity in the oxazolone model. As shown below in Table 3, both compounds inhibited ear swelling in a dose-dependent manner.

TABLE 3
		Oxazolone
		Ear Swelling %	Inhibition vs. Vehicle
Treatment	Dose (%)	Experiment 1	Experiment 2

Hydrocortisone	1	78.9	58.2
Compound 29	3	66.5	—
	1	49.9	—
	0.3	34.7	—
	0.1	4.3	—
Compound 32	3	—	36.5
	1	—	31.45
	0.3	—	18.95
	0.1	—	11.2

Both compounds were also tested in a TPA-induced ear edema model, which also shows effect of glucocorticoids. At equivalent doses, the two non-steroidal compounds were only slightly less active than hydrocortisone, as set forth in Table 4 below.

	TABLE 4
			% Inhibition of TPA Ear
	Treatment	Dose (%)	Edema vs. Vehicle
	Hydrocortisone	1	80.6
	Compound 29	1	64.9
	Compound 32	1	60.0

These tests demonstrate that the compounds of this invention (triphenylpropanamides) are topically active as antiinflammatory agents. Because of their selective effects on transcription factors, they should not cause the side effects known to be associated with classical glucocorticoids. In addition to inflammation, the triphenylpropanamides of this invention may be useful as therapeutics in other glucocorticoid-responsive skin conditions.