CA2660814C - Positively charged water-soluble prodrugs of aryl- and heteroarylpropionic acids with very fast skin penetration rate - Google Patents

Abstract

The novel positively charged pro-drugs of aryl- and heteroarylpropionic acids in the general formula (1) 'Structure 1' and general formula (2) 'Structure 2' were designed and synthesized. The compounds of the general formula (1) 'Structure 1' and general formula (2) 'Structure 2' indicated above can be prepared from functional derivatives of naproxen, suprofen, .alpha.- methyl-(p-chlorobenzoyl)-5-methoxy-2-methylindole 3-acetic acid, flurbiprofen, carprofen, pranoprofen, benoxaprofen, alminoprofen, tiaprofenic acid, pirprofen, zaltoprofen, bermoprofen, loxoprofen, indoprofen, fenclorac, oxaprozin, fenbufen, orpanoxin, ketorolac, clidanac, and related compounds, (for example acid halides or mixed anhydrides), by reaction with suitable alcohols, thiols, or amines. The positively charged amino groups of these pro-drugs not only largely increases the solubility of the drugs, but also bonds to the negative charge on the phosphate head group of membranes and pushes the pro-drug into the cytosol. The results suggest that the pro-drugs diffuses through human skin -100-130 times faster than do their parent drugs. It takes 2-4 hours for naproxen, suprofen, .alpha.- methyl-(p-chlorobenzoyl)-5-methoxy-2-methylindole 3-acetic acid, flurbiprofen, carprofen, pranoprofen, benoxaprofen, alminoprofen, tiaprofenic acid, pirprofen, zaltoprofen, bermoprofen, loxoprofen, indoprofen, fenclorac, oxaprozin, fenbufen, orpanoxin, ketorolac, clidanac, and related compounds to reach the peak plasma level when they are taken orally, but these prodrugs only took about 40-50 minutes to reach the peak plasma level when they are taken transdermally. In plasma, more than 90% of these pro-drugs can change back to the drug in a few minutes. The prodrugs can be used medicinally in treating any NS AIAs-treatable conditions in humans or animals. The prodrugs can be administered not only orally, but also transdermally for any kind of medical treatments and avoid most of the side effects of NSAIAs, most notably GI disturbances such as dyspepsia, gastroduodenal bleeding, gastric ulcerations, and gastritis. Controlled transdermal administration systems of the prodrugs enable naproxen, suprofen, .alpha.- methyl-(p-chlorobenzoyl)-5-methoxy-2-methylindole 3-acetic acid, flurbiprofen, carprofen, pranoprofen, benoxaprofen, alminoprofen, tiaprofenic acid, pirprofen, zaltoprofen, bermoprofen, loxoprofen, indoprofen, fenclorac, oxaprozin, fenbufen, orpanoxin, ketorolac, clidanac, and related compounds to reach constantly optimal therapeutic blood levels to increase effectiveness and reduce the side effects of NSAIAs. Another great benefit of transdermal administration of these pro-drugs is that administering medication, especially to children, will be much easier.

Description

Description POSITIVELY CHARGED WATER-SOLUBLE PRODRUGS OF
ARYL- AND HETEROARYLPROPIONIC ACIDS WITH VERY
FAST SKIN PENETRATION RATE
Technical Field [1] The present invention relates to the preparations of positively charged and water-soluble pro-drugs of aryl- and heteroarylpropionic acids and related compounds and their medicinal use in treating any nonsteroidal anti-inflammatory drugs (NSAIAs)-treatable conditions in humans or animals. More specifically, the present invention is to overcome the side effects that are associated with the use of NSAIAs.
These pro-drugs can be administered orally or transdermally.
Background Art

[2] There are 2-aryl- and heteroarylpropionic acids, 3-aryl- and heteroarylpropionic acids and cyclized aryl- and heteroarylpropionic acids. 2-(6-methoxy-2-naphthyl) propionic acid (naproxen), a-methyl-4-(2-thienylcarbonyl)benzeneacetic acid (suprofen), a-methyl-(p-chlorobenzoy1)-5-methoxy-2-methylindole-3-acetic acid, 2-(2-fluoro-4-biphenylyl)propionic acid (flurbiprofen), 6-chloro-a-methyl-9H-carbazole-2-acetic acid (carprofen), a-methyl-5H-[1]
benzopyrano[2,3-131pyridine-7-acetic acid (pranoprofen), 2-(4-chloropheny1)-a-methyl-5-benzoxazoleacetic acid (benoxaprofen), a-methy1-4-[(2-methyl-2-propenypaminolbenzeneacetic acid (alminoprofen), 5-benzoyl-a-methyl-2-thiopheneacetic acid (tiaprofenic acid),

3-chloro-4-(2,5-dihydro-1H-pyrrol-1-y1)-a-methylbenzeneacetic acid (pirprofen), 2-(10, 11-dihydro-10-oxodibenzo(b,f)thiepin-2-yl)propionic acid (zaltoprofen), 2-(8-methy1-10, 11-dihydro-11-oxodibenz(b,Doxepin-2-yl)propionic acid (bermoprofen), 214-(2-oxocyclopentyl-methyl)phenyllpropionic acid (loxoprofen),

4-(1,3-dihydro-1-oxo-2H-isoindo1-2-y1)-a-methylbenzeneacetic acid (indoprofen), a,3-dichloro-4-cyclohexylbenzeneacetic acid (fenclorac), and related compounds are members of 2-aryl and heteroarylpropionic acid group of nonsteroidal anti-inflammatory drugs. 4,5-Dipheny1-2-oxazole propionic acid (oxaprozin), 3-(4-biphenylylcarbonyl)propionic acid (fenbufen),

5-(4-chloropheny1)-beta-hydroxy-2-furanpropionic acid (orpanoxin), and related compounds are members of 3-aryl and heteroarylpropionic acid group of nonsteroidal anti-inflammatory drugs. 5-benzoy1-2,3-dihydro-1H-pyrrolizine-1-carboxylic acid (ketorolac), 6-chloro-5-cyclohexy1-2,3-dihydro-1H-indene-1-carboxylic acid (clidanac), and related compounds are members of cyclized aryl- and heteroaryl-propionic acid group of nonsteroidal anti-inflammatory drugs. They are used for the relief of signs and symptoms of rheumatoid arthritis and osteoartluitis and for the treatment of dysmenorrhea. They are also used for the treatment of acute gouty arthritis and ankylosing spondylitis. The may be used for the treatment of dementia (McGeer;
Patrick L. et al. U.S. Pat. No. 5,192,753).
[3] Unfortunately, a number of side effects are associated with the use of naproxen, suprofen, a-methyl-(p-chlorobenzoy1)-5-methoxy-2-methylindole 3-acetic acid, flurbiprofen, carprofen, pranoprofen, benoxaprofen, alminoprofen, tiaprofenic acid, pirprofen, zaltoprofen, bermoprofen, loxoprofen, indoprofen, fenclorac, oxaprozin, fenbufen, orpanoxin, ketorolac, clidanac, and related compounds, most notably GI dis-turbances such as dyspepsia, gastroduodenal bleeding, gastric ulcerations, and gastritis.
Fishman (Fishman; Robert, U.S. Pat. No. 7,052,715) indicated that an additional problem associated with oral medications, is that the concentration levels which must be achieved in the bloodstream must be significant in order to effectively treat distal areas of pain or inflammation. These levels are often much higher than would be necessary if it were possible to accurately target the particular site of pain or injury.
Fishman and many others (Van Engelen et al. U.S. Pat. No. 6,416,772; Macrides et al.
U.S. Pat. No. 6,346,278; Kirby et al. U.S. Pat. No. 6,444,234, Roentsch, et al., U.S.
Pat. No. 5,654,337, Park, et al., U.S. Pat. No. 6,190,690, Pearson et al. U.S.
Pat. No.

6,528,040 and Botknecht et al. U.S. Pat. No. 5,885,597) have tried to develop a delivery system for transdermal application by formulation. It is very difficult, however, to deliver therapeutically effective plasma levels of these kind drugs into the host by formulation, due to the slow skin penetration rate. Susan Milosovich, et al.
designed and prepared testosterony1-4-dimethylaminobutyrate.HC1 (TSBH), which has a lipophilic portion and a tertiary amine groups that exists in the protonated form at physiological pH. They found that the prodrug (TSBH) diffuses through human skin -60 times faster than does the drug (TS) itself [Susan Milosovich, et al., J.
Pharm. Sci., 82, 227(1993).
Disclosure of Invention Technical Problem [4] Naproxen, suprofen, a-methyl-(p-chlorobenzoy1)-5-methoxy-2-methylindole 3-acetic acid, flurbiprofen, carprofen, pranoprofen, benoxaprofen, alminoprofen, tiaprofenic acid, pitprofen, zaltoprofen, bermoprofen, loxoprofen, indoprofen, fenclorac, oxaprozin, fenbufen, orpanoxin, ketorolac, clidanac, and related compounds, have been used medicinally for many years. They are used for the relief of signs and symptoms of rheumatoid arthritis and osteoarthritis, for the treatment of dysmenorrhea.
[5] Unfortunately, a number of side effects are associated with the use of NSAIAs, most notably GI disturbances such as dyspepsia, gastroduodenal bleeding, gastric ul-cerations, and gastritis. They are not soluble in aqueous solution and gastric juice.
They stay in the GI tract for a long time and thus, may cause gastric mucosal cell damage.
Technical Solution [6] This invention relates to the preparation of novel positively charged pro-drugs of aryl- and heteroarylpropionic acids and related compounds and their use medicinally.
2-(6-methoxy-2-naphthyl)propionic acid (naproxen), a-methy1-4-(2-thienylcarbonyl)benzeneacetic acid (suprofen), cc-methyl-(p-chlorobenzoy1)-5-methoxy-2-methylindole 3-acetic acid, 2-(2-fluoro-4-biphenylyl)propionic acid (flurbiprofen), 6-chloro-a-methyl-9H-carbazole-2-acetic acid (carprofen), a-methyl-5H-[1]
benzopyrano[2,3-b]pyridine-7-acetic acid (pranoprofen), 2-(4-chloropheny1)-a-methyl-5-benzoxazoleacetic acid (benoxaprofen), cc-methy1-4-[(2-methyl-2-propenypaminolbenzeneacetic acid (alminoprofen), 5-benzoyl-a-methyl-2-thiopheneacetic acid (tiaprofenic acid), 3-chloro-4-(2,5-dihydro-1H-pyrrol-1-y1)-a-methyl benzeneacetic acid (piiprofen), 2-(10, 11-dihydro-10-oxodibenzo(b,f)thiepin-2-yl)propionic acid (zaltoprofen), 2-(8-methy1-10, 11-dihydro-11-oxodibenz(b,Doxepin-2-yl)propionic acid (bermoprofen), 214-(2-oxocyclopentyl-methyl)phenyl]propionic acid (loxoprofen), 4-(1,3-dihydro-1-oxo-2H-isoindo1-2-y1)-a-methylbenzeneacetic acid (indoprofen), a,3-dichloro-4-cyclohexylbenzeneacetic acid (fenclorac), and related compounds are member s of 2-aryl and heteroarylpropionic acid group of nonsteroidal anti-inflammatory drugs. The pro-drugs of 2-aryl- and heteroarylpropionic acids have the general formula (1) "Structure 1", A Ri 'X
Aryl cNR2 \R3 Structure 1 In structure 1, R represents CH, OH, Cl, F, or Br; Ri represents H, one of any alkyl, alkyloxyl, alkenyl or alkynyl residues having 1 to 12 carbon atoms, or aryl residues; R2 represents H, one of any alkyl, alkyloxy, alkenyl or alkynyl residues having 1 to 12 carbon atoms, or aryl residues; R3 represents H, one of any alkyl, alkyloxy, alkenyl or alkynyl residues having 1 to 12 carbon atoms, or aryl residues; X represents 0, S, NH, OCH COO, OCH COS, or OCH CONH; A- represents Cl-, Br, F, r, Ac0-, citrate, or any negative ions; and n=0,1, 2, 3, 4, 5, 6, 7, 8, 9, 10 ; Aryl represents:
14001 s In which, X represents CH30, Cl, F, CH3S, Y
R
C=0 X
In which, X represents F, Cl. H
In which, Y represents CH30, F, CH3CO, (CH3)2N, CH3, or CH2¨CH-CH2, X represents Cl, F, CF3, CH3S0,or CI-13S; R represents CH3, C2Hs, C3H7 In which, X represents Cl, Br, F, CH3 \o In which_ X represents Cl, Br, F, CH3 N
X
In which, X represents Cl, F, Br X
N
o In which, X represents Cl, Br, F, or CH30 In which, X represents CO or Nit Z
R x 110 =
In which, X represents 0 or S, Y represents CH, and CO, and Z represents, CO and CH,, R represents H, CH3, C4-15 All R groups may include C, H, 0, S, or N atoms and may have single, double, and treble bonds. Any CH2 groups may be replaced with 0, S, or NH.

[7] 4,5-Dipheny1-2-oxazole propionic acid (oxaprozin), 3-(4-biphenylylcarbonyl)propionic acid (fenbufen), 5-(4-chloropheny1)-beta-hydroxy-2-furanpropanoic acid (orpanoxin), and related compounds are members of 3-aryl and heteroarylpropionic acid group of nonsteroidal anti-inflammatory drugs. The pro-drugs of 3-aryl- and heteroarylpropionic acids have the general formula (2) 'Structure 2'.
A Ri N ¨ R2 \ R3 Structure 2 In structure 2, W represents H, OH, Cl, F, or Br; Ri represents H, one of any alkyl, alkyloxyl, alkenyl or alkynyl residues having 1 to 12 carbon atoms, or aryl residues; R2 represents H, one of any alkyl, alkyloxy, alkenyl or alkynyl residues having 1 to 12 carbon atoms, or aryl residues; R3 represents H, one of any alkyl, alkyloxy, alkenyl or alkynyl residues having 1 to 12 carbon atoms, or aryl residues; X represents 0, S, NH, OCH COO, OCH COS, or OCH CONH; A- represents Cl-, Br-, F, r, Ac0-, citrate, or any negative ions; and n=0,1,2,3,4,5,6,7,8,9,10 ................... ; W
represents OH, Cl, or F; Y
represents H, Cl, OH, or CH; and Z represents:

x ___________________________________________________________ oN
In which, X represents Cl, F, or Br All R, R, R, R' and R groups may include C, H, 0, S, N atoms and may have single, double, and treble bonds. Any CH2 groups may be replaced with 0, S, or NH.

[8] In the general formula (2) 'Structure 2', when W represents H, Y and Z together represent:

X (Y) (Y) 1110 (Z) (Z) In which, X represents Cl, F, or Br The cyclized aryl- and heteroarylpropionic acid are formed. They are 5-benzoy1-2,3-dihydro-1H-pyrrolizine-1-carboxylic acid (ketorolac), 6-chloro-5-cyclohexy1-2,3-dihydro-1H-indene-1-carboxylic acid (clidanac) and related compounds.

[9] Drug absorption, whether from the gastrointestinal tract or other sites, requires the passage of the drug in a molecular form across the barrier membrane. The drug must first dissolve, and if the drug possesses the desirable biopharmaceutical properties, it will pass from a region of high concentration to a region of low concentration across the membrane into the blood or general circulation. All biological membranes contain lipids as major constituents. The molecules that play the dominant roles in membrane formation all have phosphate-containing highly polar head groups, and, in most cases, two highly hydrophobic hydrocarbon tails. Membranes are bilayers, with the hy-drophilic head groups facing outward into the aqueous regions on either side.
Very hy-drophilic drugs cannot pass the hydrophobic layer of membrane and very hydrophobic drugs will stay in the hydrophobic layer as part of the membrane due to their sim-ilarities and cannot enter the cytosol on the inside efficiently.

[10] The goal of this invention is to avoid the side effects of naproxen, suprofen, a-methyl-(p-chlorobenzoy1)-5-methoxy-2-methylindole 3-acetic acid, flurbiprofen, carprofen, pranoprofen, benoxaprofen, alminoprofen, tiaprofenic acid, pirprofen, zaltoprofen, bermoprofen, loxoprofen, indoprofen, fenclorac, oxaprozin, fenbufen, orpanoxin, ketorolac, clidanac, and related compounds by increasing the their solubility in gastric juice and their penetration rate through the membrane and skin barrier which will make it administrable transdermally (topical application).
These novel pro-drugs have two structural features in common: they have a lipophilic portion and a primary, secondary, or tertiary amine group that exists in the protonated form (hydrophilic part) at physiological pH. Such a hydrophilic-lipophilic balance is required for efficient passage through the membrane barrier [Susan Milosovich, et al., J. Phann. Sci., 82, 227(1993)1. The positively charged amino groups largely increase the solubility of the drugs. The solubility of diethylaminoethyl 2-(6-methoxy-2-naphthyl)propionate.AcOH, diethylaminoethyl a-methy1-442-thienylcarbonyl)benzeneacetate.AcOH, diethylaminoethyl a-methyl4p-chlorobenzoy1)-5-methoxy-2-methylindole 3-acetate.AcOH, diethy-laminoethyl 2-(2-fluoro-4-biphenylyl)propionate.AcOH, diethylaminoethyl 6-chloro-a-methyl-9H-carbazole-2-acetate.AcOH, diethylaminoethyl a-methy1-5H-[1]
benzopyrano[2,3-blpyridine-7-acetate.AcOH, diethylaminoethyl 2(4-chloropheny1)-a-methy1-5-benzoxazoleacetate.AcOH, diethylaminoethyl a-methy1-44(2-methyl-2-propenypaminolbenzeneacetate.AcOH, diethylaminoethyl 5-benzoyl-a-methyl-2-thiopheneacetate.AcOH, diethylaminoethyl 3-chloro-4-(2,5-dihydro-1H-pyrrol-1-y1)-a-methyl benzeneacetate.AcOH, diethy-laminoethyl 2-(10, 11-dihydro-10-oxodibenzo(b,f)thiepin-2-yl)propionate.AcOH, di-ethylaminoethyl 248-methy1-10,

11-dihydro-11-oxodibenz(b,f)oxepin-2-yl)propionate.AcOH, diethylaminoethyl 2[4(2-oxocyclopentyl-methyl)phenyllpropionate.AcOH, diethylaminoethyl 4-(1,3-dihydro-1-oxo-2H-isoindo1-2-y1)-a-methylbenzeneacetate.AcOH, diethy-laminoethyl a,3-dichloro-4-cyclohexylbenzeneacetate.AcOH, diethylaminoethyl 4,5-Dipheny1-2-oxazole propionate.AcOH, diethylaminoethyl 3(4-biphenylylcarbonyl)propionate.AcOH, diethylaminoethyl 5-(4-chloropheny1)-beta-hydroxy-2-furanpropionate.AcOH, diethylaminoethyl 5-benzoy1-2,3-dihydro-1H-pyrrolizine-1-carboxylate.AcOH, diethylaminoethyl 6-chloro-5-cyclohexy1-2,3-dihydro-1H-indene-1-carboxylate.AcOH, naproxen, suprofen, a-methyl(p-chlorobenzoy1)-5-methoxy-2-methylindole 3-acetic acid, flurbiprofen, carprofen, pranoprofen, benoxaprofen, alminoprofen, tiaprofenic acid, pirprofen, zaltoprofen, bermoprofen, loxoprofen, indoprofen, fenclorac, oxaprozin, fenbufen, orpanoxin, ketorolac, clidanac in water are >450 mg, >400 mg, >450 mg, >
450 mg, >350 mg, >450 mg, >400 mg, >450 mg, >400 mg, >450 mg, >350 mg, >400 mg, >350 mg, >400 mg, >350 mg, >400 mg, >400 mg, >350 mg, >450 mg, >350 mg, <0.1 mg, <0.1 mg, <0.1 mg, <0.1 mg, <0.1 mg, <0.1 mg, <0.1 mg, <0.1 mg, <0.1 mg, <0.1 mg, <0.1 mg, <0.1 mg, <0.1 mg, <0.1 mg, <0.1 mg, <0.1 mg, <0.1 mg, <0.1 mg, <0.1 mg, and <0.1 mg/ml, In many instances, the lowest or rate-limiting step in the sequence is the dissolution of the drug. Naproxen, suprofen, a-methyl4p-chlorobenzoy1)-5-methoxy-2-methylindole 3-acetic acid, flurbiprofen, carprofen, pranoprofen, benoxaprofen, alminoprofen, tiaprofenic acid, pirprofen, zaltoprofen, bermoprofen, loxoprofen, indoprofen, fenclorac, oxaprozin, fenbufen, orpanoxin, ketorolac, clidanac, and related compounds have a very low solubility in gastric juice. They stay in the GI tract for a long time and thus, may cause gastric mucosal cell damage. When these new pro-drugs are administered orally in a dosage form such as a tablet, capsule, solution, or suspension, they will dissolve in the gastric juice immediately. The positive charge on the amino groups of these pro-drugs will bond to the negative charge on the phosphate head group of membrane. Thus, the local concentration of the outside of the membrane will be very high and will facilitate the passage of these pro-drugs from a region of high concentration to a region of low con-centration. When these pro-drugs enter the membrane, the hydrophilic part will push the pro-drug into the cytosol, a semi-liquid concentrated aqueous solution or suspension. Due to the short stay in GI tract, the pro-drugs will not cause gastric mucosal cell damage. The pH of the stomach is 1-3, so the negative charge on the phosphate head group of membrane is bonded with proton (M. The positive charges of prodrugs cannot bond to the negative charge on the phosphate head group of the gastric mucosa. These prodrugs will be free both of primary insult (direct acid damage) and secondary insult (prostaglandin inhibition) to the stomach.
1111 The penetration rates of aryl- and heteroarylpropionic acids and their positively charged prodrugs and related compounds through human skin were measured in vitro by using modified Franz cells, which were isolated from human skin tissue (360-pm thick) of the anterior and posterior thigh areas. The receiving fluid consisted of 10 ml of 2% bovine serum albumin in normal saline and was stirred at 600 rpm. The cumulative amounts of these prodrugs and their parent drugs penetrating the skin versus time were determined by a specific high-performance liquid chromatography method. The results using a donor consisting of either a 30% solution of these prodrugs or a 30% suspension of naproxen, suprofen, a-methyl-(p-chlorobenzoy1)-5-methoxy-2-methylindole 3-acetic acid, flurbiprofen, carprofen, pranoprofen, benoxaprofen, alminoprofen, tiaprofenic acid, pirprofen, zaltoprofen, bermoprofen, loxoprofen, indoprofen, fenclorac, oxaprozin, fenbufen, orpanoxin, ketorolac, clidanac in 2mL of pH 7.4 phosphate buffer (0.2M) are shown in Figure 1, Figure 2, Figure 3, or Figure 4. Apparent flux values of 3.5 mg, 3.0 mg, 4.0 mg, 3.5 mg, 4.0 mg, 3.8 mg, 4.0 mg, 3.5 mg, 4.2 mg, 3.5 mg, 3.7 mg, 4.1 mg, 3.4 mg, 4.2 mg, 3.8 mg, 4.0 mg, 3.6 mg, 4.1 mg, 3.8 mg, 4.0 mg, 0.03 mg, 0.03 mg, 0.03 mg, 0.03 mg, 0.04 mg, 0.03 mg, 0.04 mg, 0.03 mg, 0.03 mg, 0.03 mg, 0.03 mg, 0.04 mg, 0.03 mg, 0.03 mg, 0.04 mg, 0.03 mg, 0.04 mg, 0.03 mg, 0.03 mg, and 0.04 mg/cm2/h were calculated for diethylaminoethyl 2-(6-methoxy-2-naphthyl)propionate.AcOH, di-ethylaminoethyl a-methyl-4-(2-thienylcarbonyl)benzeneacetate.AcOH, diethy-laminoethyl a-methyl-(p-chlorobenzoy1)-5-methoxy-2-methylindole 3-acetate.AcOH, diethylaminoethyl 2-(2-fluoro-4-biphenylyl)propionate.AcOH, diethylaminoethyl 6-chloro-a-methyl-9H-carbazole-2-acetate.AcOH, diethylaminoethyl a-methy1-5H-[1]
benzopyrano[2,3-blpyridine-7-acetate.AcOH, diethylaminoethyl 2-(4-chloropheny1)-a-methyl-5-benzoxazoleacetate.AcOH, diethylaminoethyl a-methyl-4-[(2-methyl-2-propenypaminolbenzeneacetate.AcOH, diethylaminoethyl 5-benzoyl-a-methyl-2-thiopheneacetate.AcOH, diethylaminoethyl 3-chloro-4-(2,5-dihydro-1H-pyrrol-1-y1)-a-methyl benzeneacetate.AcOH, diethy-laminoethyl 2-(10, 11-dihydro-10-oxodibenzo(b,f)thiepin-2-yl)propionate.AcOH, di-ethylaminoethyl 248-methy1-10, 11-dihydro-11-oxodibenz(b,f)oxepin-2-yl)propionate.AcOH, diethylaminoethyl 2[4(2-oxocyclopentyl-methyl)phenyllpropionate.AcOH, diethylaminoethyl 4-(1,3-dihydro-1-oxo-2H-isoindo1-2-y1)-a-methylbenzeneacetate.AcOH, diethy-laminoethyl a,3-dichloro-4-cyclohexylbenzeneacetate.AcOH, diethylaminoethyl 4,5-Dipheny1-2-oxazole propionate.AcOH, diethylaminoethyl 3(4-biphenylylcarbonyl)propionate.AcOH, diethylaminoethyl 5(4-chloropheny1)-beta-hydroxy-2-furanpropionate.AcOH, diethylaminoethyl 5-benzoy1-2,3-dihydro-1H-pyrrolizine-1-carboxylate.AcOH, diethylaminoethyl 6-chloro-5-cyclohexy1-2,3-dihydro-1H-indene-1-carboxylate.AcOH, naproxen, suprofen, a-methyl(p-chlorobenzoy1)-5-methoxy-2-methylindole 3-acetic acid, flurbiprofen, carprofen, pranoprofen, benoxaprofen, alminoprofen, tiaprofenic acid, pirprofen, zaltoprofen, bermoprofen, loxoprofen, indoprofen, fenclorac, oxaprozin, fenbufen, orpanoxin, ketorolac, and clidanac diffuses through human skin. The results suggest that the pro-drug, diethylaminoethyl 2-(6-methoxy-2-naphthyl)propionate.AcOH, diethylaminoethyl a-methy1-442-thienylcarbonyl)benzeneacetate.AcOH, diethylaminoethyl a-methyl4p-chlorobenzoy1)-5-methoxy-2-methylindole 3-acetate.AcOH, diethy-laminoethyl 2-(2-fluoro-4-biphenylyl)propionate.AcOH, diethylaminoethyl 6-chloro-a-methyl-9H-carbazole-2-acetate.AcOH, diethylaminoethyl a-methy1-5H-[1]
benzopyrano[2,3-blpyridine-7-acetate.AcOH, diethylaminoethyl 2(4-chloropheny1)-a-methy1-5-benzoxazoleacetate.AcOH, diethylaminoethyl a-methy1-4-[(2-methyl-2-propenypaminolbenzeneacetate.AcOH, diethylaminoethyl 5-benzoyl-a-methyl-2-thiopheneacetate.AcOH, diethylaminoethyl 3-chloro-4-(2,5-dihydro-1H-pyrrol-1-y1)-a-methyl benzeneacetate.AcOH, diethy-laminoethyl 2-(10, 11-dihydro-10-oxodibenzo(b,f)thiepin-2-yl)propionate.AcOH, di-ethylaminoethyl 248-methy1-10, 11-dihydro-11-oxodibenz(b,f)oxepin-2-yl)propionate.AcOH, diethylaminoethyl 2[4(2-oxocyclopentyl-methyl)phenylipropionate.AcOH, diethylaminoethyl 4-(1,3-dihydro-1-oxo-2H-isoindo1-2-y1)-a-methylbenzeneacetate.AcOH, diethy-laminoethyl a,3-dichloro-4-cyclohexylbenzeneacetate.AcOH, diethylaminoethyl 4,5-Dipheny1-2-oxazole propionate.AcOH, diethylaminoethyl 3(4-biphenylylcarbonyl)propionate.AcOH, diethylaminoethyl 5(4-chloropheny1)-beta-hydroxy-2-furanpropionate.AcOH, diethylaminoethyl 5-benzoy1-2,3-dihydro-1H-pyrrolizine-1-carboxylate.AcOH, or diethylaminoethyl 6-chloro-5-cyclohexy1-2,3-dihydro-1H-indene-1-carboxylate.AcOH diffuses through human skin -100-130 times faster than does naproxen, suprofen, a-methyl4p-chlorobenzoy1)-5-methoxy-2-methylindole 3-acetic acid, flurbiprofen, carprofen, pranoprofen, benoxaprofen, alminoprofen, tiaprofenic acid, pirprofen, zaltoprofen, bermoprofen, loxoprofen, indoprofen, fenclorac, oxaprozin, fenbufen, orpanoxin, ketorolac, or clidanac . The results suggest that the positive charge on the dialkyaminoethyl group has a very important role in the passage of the drug across the membrane and skin barrier. Other prodrugs of the general 'Structure 1' or general 'St ructure 2' have very high penetration rates and are very close to that of diethy-laminoethyl 2-(6-methoxy-2-naphthyl)propionate.AcOH.

[12] The in vivo rates of penetration of aryl- and heteroarylpropionic acids and their positively charged prodrugs and related compounds through the skin of intact hairless mice were compared. The donor consisted of a 20% solution of these compounds in 1 mL of isopropanol applied to a 10 cm2 on the backs of the hairless mice.
Plasma levels of naproxen, suprofen, a-methyl(p-chlorobenzoy1)-5-methoxy-2-methylindole 3-acetic acid, flurbiprofen, carprofen, pranoprofen, benoxaprofen, alminoprofen, tiaprofenic acid, pliprofen, zaltoprofen, bermoprofen, loxoprofen, indoprofen, fenclorac, oxaprozin, fenbufen, orpanoxin, ketorolac, clidanac were determined by a specific high-performance liquid chromatography method. The results (Figure 5, Figure 6, Figure 7, Figure 8) show that the peak levels of diethylaminoethyl 2-(6-methoxy-2-naphthyl)propionate.AcOH, diethylaminoethyl a-methyl-4(2-thien ylcarbonyl)benzeneacetate.AcOH, diethylaminoethyl a-methyl4p-chlorobenzoy1)-5-methoxy-2-methylindole 3-acetate.AcOH, diethy-laminoethyl 2(2-fluoro-4-biphenylyppropionate.AcOH, diethylaminoethyl 6-chloro-a-methyl-9H-carbazole-2-acetate.AcOH, diethylaminoethyl a-methy1-5H-[1]
benzopyrano[2,3-blpyridine-7-acetate.AcOH, diethylaminoethyl 2(4-chloropheny1)-a-methy1-5-benzoxazoleacetate.AcOH, diethylaminoethyl a-methy1-41(2-methyl-2-propenypaminolbenzeneacetate.AcOH, diethylaminoethyl 5-benzoyl-a-methyl-2-thiopheneacetate.AcOH, diethylaminoethyl 3-chloro-4-(2,5-dihydro-1H-pyrrol-1-y1)-a-methyl benzeneacetate.AcOH, diethy-laminoethyl 2-(10, 11-dihydro-10-oxodibenzo(b,f)thiepin-2-yl)propionate.AcOH, di-ethylaminoethyl 248-methy1-10, 11-dihydro-11-oxodibenz(b,f)oxepin-2-yl)propionate.AcOH, diethylaminoethyl 2[4(2-oxocyclopentyl-methyl)phenylipropionate.AcOH, diethylaminoethyl 4-(1,3-dihydro-1-oxo-2H-isoindo1-2-y1)-a-methylbenzeneacetate.AcOH, diethy-laminoethyl a,3-dichloro-4-cyclohexylbenzeneacetate.AcOH, diethylaminoethyl 4,5-Dipheny1-2-oxazole propionate.AcOH, diethylaminoethyl 3(4-biphenylylcarbonyl)propionate.AcOH, diethylaminoethyl 5(4-chloropheny1)-beta-hydroxy-2-furanpropionate.AcOH, diethylaminoethyl 5-benzoy1-2,3-dihydro-1H-pyrrolizine-1-carboxylate.AcOH, diethylaminoethyl 6-ch loro-5-cyclohexy1-2,3-dihydro-1H-indene-1-carboxylate.AcOH were reached -50 minutes after application of the donor systems. It takes 2-4 hours for naproxen, suprofen, a-methyl(p-chlorobenzoy1)-5-methoxy-2-methylindole 3-acetic acid, flurbiprofen, carprofen, pranoprofen, benoxaprofen, alminoprofen, tiaprofenic acid, pirprofen, zaltoprofen, bermoprofen, loxoprofen, indoprofen, fenclorac, oxaprozin, fenbufen, orpanoxin, ketorolac, clidanac to reach their peak plasma level when they are taken orally. The peak plasma levels were -0.01 mg/ml for naproxen, suprofen, a-methyl4p-chlorobenzoy1)-5-methoxy-2-methylindole 3-acetic acid, flurbiprofen, carprofen, pranoprofen, benoxaprofen, alminoprofen, tiaprofenic acid, pirprofen, zaltoprofen, bermoprofen, loxoprofen, indoprofen, fenclorac, oxaprozin, fenbufen, orpanoxin, ketorolac, clidanac and -2 mg/ml for diethylaminoethyl 2-(6-methoxy-2-naphthyl)propionate.AcOH, diethylaminoethyl a-methy1-442-thienylcarbonyl)benzeneacetate.AcOH, diethylaminoethyl a-methyl4p-chlorobenzoy1)-5-methoxy-2-methylindole 3-acetate.AcOH, diethy-laminoethyl 2-(2-fluoro-4-biphenylyl)propionate.AcOH, diethylaminoethyl 6-chloro-a-methyl-9H-carbazole-2-acetate.AcOH, diethylaminoethyl a-methy1-5H-[1]
benzopyrano[2,3-blpyridine-7-acetate.AcOH, diethylaminoethyl 2(4-chloropheny1)-a-methy1-5-benzoxazoleacetate.AcOH, diethylaminoethyl a-methy1-4-[(2-methyl-2-propenypaminolbenzeneacetate.AcOH, diethylaminoethyl 5-benzoyl-a-methyl-2-thiopheneacetate.AcOH, diethylaminoethyl 3-chloro-4-(2,5-dihydro-1H-pyrrol-1-y1)-a-methyl benzeneacetate.AcOH, diethy-laminoethyl 2-(10, 11-dihydro-10-oxodibenzo(b,f)thiepin-2-yl)propionate.AcOH, di-ethylaminoethyl 248-methy1-10, 11-dihydro-11-oxodibenz(b,f)oxepin-2-yl)propionate.AcOH, diethylaminoethyl 2[4(2-oxocyclopentyl-methyl)phenylipropionate.AcOH, diethylaminoethyl 4-(1,3-dihydro-1-oxo-2H-isoindo1-2-y1)-a-methylbenzeneacetate.AcOH, diethy-laminoethyl a,3-dichloro-4-cyclohexylbenzeneacetate.AcOH, diethylaminoethyl 4,5-Dipheny1-2-oxazole propionate.AcOH, diethylaminoethyl 3-(4-biphenylylcarbonyl)propionate.AcOH, diethylaminoethyl 5(4-chloropheny1)-beta-hydroxy-2-furanpropionate.AcOH, diethylaminoethyl 5-benzoy1-2,3-dihydro-1H-pyrrolizine-1-carboxylate.AcOH, or diethylaminoethyl 6-chloro-5-cyclohexy1-2,3-dihydro-1H-indene-1-carboxylate.AcOH (approximately 200 times difference). -2 mg,/m1 of naproxen, suprofen, a-methyl4p-chlorobenzoy1)-5-methoxy-2-methylindole 3-acetic acid, flurbiprofen, carprofen, pranoprofen, benoxaprofen, alminoprofen, tiaprofenic acid, pirprofen,

13 zaltoprofen, bermoprofen, loxoprofen, indoprofen, fenclorac, oxaprozin, fenbufen, orpanoxin, ketorolac, clidanac in plasma is more than 20-100 times higher than plasma level for effective analgesia and effective anti-inflammatory activity. This is a very exciting result. It will be very easy and fast to deliver therapeutically effective plasma level of naproxen, suprofen, a-methyl(p-chlorobenzoy1)-5-methoxy-2-methylindole 3-acetic acid, flurbiprofen, carprofen, pranoprofen, benoxaprofen, alminoprofen, tiaprofenic acid, pirprofen, zaltoprofen, bermoprofen, loxoprofen, indoprofen, fenclorac, oxaprozin, fenbufen, orpanoxin, ketorolac, clidanac into the host by admin-istration of these prodrugs transdennally. These results suggest that the pro-drugs can be administered not only orally, but also transdermally for any kind of medical treatments. The in vivo rates of penetration of other Pro-drugs of the general 'Structure 1' or general 'Structure 2' are close to that of diethylaminoethyl 2-(6-methoxy-2-naphthyl)propionate.AcOH.
1-131 To check the gastroduodenal bleeding caused by these prodrugs, rats were orally administered with 50 mg/kg of diethylaminoethyl 2-(6-methoxy-2-naphthyl )propionate.AcOH, diethylaminoethyl a-methy1-442-thienylcarbonyl)benzeneacetate.AcOH, diethylaminoethyl a-methyl-(p-chlorobenzoy1)-5-methoxy-2-methylindole 3-acetate.AcOH, diethy-laminoethyl 2-(2-fluoro-4-biphenylyl)propionate.AcOH, diethylaminoethyl 6-chloro-a-methyl-91-1-carbazole-2-acetate.AcOH, diethylaminoethyl a-methyl-51141]
benzopyrano[2,3-blpyridine-7-acetate.AcOH, diethylaminoethyl 2(4-chloropheny1)-a-methy1-5-benzoxazoleacetate.AcOH, diethylaminoethyl a-methy1-4-[(2-methyl-2-propenyDaminolbenzeneacetate.AcOH, diethylaminoethyl 5-benzoyl-a-methyl-2-thiopheneacetate.AcOH, diethylaminoethyl 3-chloro-4-(2,5-dihydro-1H-pyrrol-1-y1)-a-methyl benzeneacetate.AcOH, diethy-laminoethyl 2-(10, 11-dihydro-10-oxodibenzo(b,f)thiepin-2-yl)propionate.AcOH, di-ethylaminoethyl 248-methy1-10, 11-dihydro-11-oxodibenz(b,f)oxepin-2-yl)propionate.AcOH, diethylaminoethyl 2[4(2-oxocyclopentyl-methyl)phenyllpropionate.AcOH, diethylaminoethyl 441 ,3-dihydro-l-oxo-2H-i soindo1-2-y1)-a-methylbenzeneacetate.AcOH, diethy-laminoethyl a,3-dichloro-4-cyclohexylbenzeneacetate.AcOH, diethylaminoethyl 4,5-Dipheny1-2-oxazole propionate.AcOH, diethylaminoethyl 3(4-biphenylylcarbonyl)propionate.AcOH, diethylaminoethyl 5(4-chloropheny1)-beta-hydroxy-2-furanpropionate.AcOH, diethylaminoethyl 5-benzoy1-2,3-dihydro-1H-pyrrolizine-1-carboxylate.AcOH, diethylaminoethyl 6-chloro-5-cyclohexy1-2,3-dihydro-1H-indene-1-carboxylate.AcOH, naproxen, suprofen, a-methyl(p-chlorobenzoy1)-5-methoxy-2-methylindole 3-acetic acid, flurbiprofen, carprofen, pranoprofen, benoxaprofen, ahninoprofen, tiaprofenic acid,

14 pirprofen, zaltoprofen, bermoprofen, loxoprofen, indoprofen, fenclorac, oxaprozin, fenbufen, orpanoxin, ketorolac, clidanac per day for 21 days. We found an average of 1-4 mg of fecal blood per gram of feces in the naproxen, suprofen, a-methyl4p-chlorobenzoy1)-5-methoxy-2-methylindole 3-acetic acid, flurbiprofen, carprofen, pranoprofen, benoxaprofen, alminoprofen, tiaprofenic acid, pirprofen, zaltoprofen, bermoprofen, loxoprofen, indoprofen, fenclorac, oxaprozin, fenbufen, orpanoxin, ketorolac, clidanac groups and none in diethylaminoethyl 2-(6-methoxy-2-naphthyl)propionate.AcOH, diethylaminoethyl a-methy1-442-thienylcarbonyl)benzeneacetate.AcOH, diethylaminoethyl a-methyl4p-chlorobenzoy1)-5-methoxy-2-methylindole 3-acetate.AcOH, diethy-laminoethyl 2-(2-fluoro-4-biphenylyl)propionate.AcOH, diethylaminoethyl 6-chloro-a-methyl-9H-carbazole-2-acetate.AcOH, diethylaminoethyl a-methyl-benzopyrano[2,3-blpyridine-7-acetate.AcOH, diethylaminoethyl 2(4-chloropheny1)-a-methy1-5-benzoxazoleacetate.AcOH, diethylaminoethyl a-methy1-44(2-methy1-2-propenyflaminoThenzeneacetate.AcOH, diethylaminoethyl 5-benzoyl-a-methyl-2-thiopheneacetate.AcOH, diethylaminoethyl 3-chloro-4-(2,5-dihydro-1H-pyrrol-1-y1)-a-methyl benzeneacetate.AcOH, diethy-laminoethyl 2-(10, 11-dihydro-10-oxodibenzo(b,f)thiepin-2-yl)propionate.AcOH, di-ethylaminoethyl 248-methy1-10, 11-dihydro-11-oxodibenz(b,f)oxepin-2-yl)propionate.AcOH, diethylaminoethyl 2[4(2-oxocyclopentyl-methyl)phenylipropionate.AcOH, diethylaminoethyl 4-(1,3-dihydro-1-oxo-2H-isoindo1-2-y1)-a-methylbenzeneacetate.AcOH, diethy-laminoethyl a,3-dichloro-4-cyclohexylbenzeneacetate.AcOH, diethylaminoethyl 4,5-Dipheny1-2-oxazole propionate.AcOH, diethylaminoethyl 3(4-biphenylylcarbonyl)propionate.AcOH, diethylaminoethyl 5(4-chloropheny1)-beta-hydroxy-2-furanpropionate.AcOH, diethylaminoethyl 5-benzoy1-2,3-dihydro-1H-pyrrolizine-1-carboxylate.AcOH, diethylaminoethyl 6-chloro-5-cyclohexy1-2,3-dihydro-1H-indene-1-carboxylate.AcOH groups.
[141 The acute toxicity of the prodrugs was investigated. The LD50 orally in mice are:
2.2 g/kg, 0.8 g/kg, 0.7g/kg , 0.75 g/kg , 1.3 g/kg , 3.5 g/kg, 1.1 g/kg, 0.6 g/kg, 0.2 g/kg for diethylaminoethyl 2(6-methoxy-2-naphthyppropionate.AcOH, diethylaminoethyl a-methyl-4(2-thienylcarbonyl)benzeneacetate.AcOH, diethylaminoethyl 6-chloro-a-methyl-9H-carbazole-2-acetate.AcOH, diethylaminoethyl a-methyl-benzopyrano[2,3-bipyridine-7-acetate.AcOH, diethylaminoethyl 2(4-chloropheny1)-a-methy1-5-benzoxazoleacetate.AcOH, diethylaminoethyl 4-(1,3-dihydro-1-oxo-2H-isoindo1-2-y1)-a-methylbenzeneacetate.AcOH, diethy-laminoethyl a-methy1-44(2-methyl-2-propenyl)aminolbenzeneacetate.AcOH, diethy-laminoethyl a,3-dichloro-4-cyclohexylbenzeneacetate.AcOH, diethylaminoethyl 6-chloro-5-cyclohexy1-2,3-dihydro-1H-indene-1-carboxylate.AcOH. The results show that the prodrugs are less toxic than their parent drugs, naproxen (LD50=1.234 g/kg), suprofen (LD50=0.59 g/kg), carprofen (400 mg/kg), pranoprofen (447 mg/kg), benoxaprofen (LD5o=0.8 g/kg), alminoprofen (LD50=2400 mg/kg), indoprofen (LD50 =0.7 mg/kg), fenclorac (LD50=0.43 g/kg), clidanac (LD50=0.035 g/kg).

[15] Naproxen, suprofen, a-methyl(p-chlorobenzoy1)-5-methoxy-2-methylindole 3-acetic acid, flurbiprofen, carprofen, pranoprofen, benoxaprofen, alminoprofen, tiaprofenic acid, piiprofen, zaltoprofen, bermoprofen, loxoprofen, indoprofen, fenclorac, oxaprozin, fenbufen, orpanoxin, ketorolac, or clidanac have demonstrated anti-inflammatory, analgesic, antipyretic, and antirheumatic activity. A good prodrug should go back to the parent drug in plasma. Diethylaminoethyl ester group of these prodrugs can be rapidly cleaved by the enzymes in human plasma in vitro and more than 90% of the pro-drugs are changed back to their parent drugs. Due to the pro-drugs having a much better absorption rate, the prodrugs will have more strength than their parent drugs at the same dosage. The analgetic, antipyretic, and anti-inflammatory activities of these prodrugs were tested using naproxen, suprofen, a-methyl4p-chlorobenzoy1)-5-methoxy-2-methylindole 3-acetic acid, flurbiprofen, carprofen, pranoprofen, benoxaprofen, alminoprofen, tiaprofenic acid, pirprofen, zaltoprofen, bermoprofen, loxoprofen, indoprofen, fenclorac, oxaprozin, fenbufen, orpanoxin, ketorolac, or clidanac as a comparison.

[16] Analgetic activity: The prolongation time of the pain threshold of a mouse tail was determined in accordance with the D'Amour-Smith Method (J. Pharmacol. Exp.
Ther., 72, 74(1941)). After 50mg/kg of these prodrugs were administered transdennally, the tails of mice were exposed to heat and the prolongation time of pain threshold was determined. The results obtained are shown in Figure 9, Figure 10, Figure 11, and Figure 12. Diethylaminoethyl 2-(6-methoxy-2-naphthyl)propionate.AcOH, diethy-laminoethyl a-methyl-4(2-thienylcarbonyl)benzeneacetate.AcOH, diethylaminoethyl a-methyl(p-chlorobenzoy1)-5-methoxy-2-methylindole 3-acetate.AcOH, diethy-laminoethyl 2-(2-fluoro-4-biphenylyl)propionate.AcOH, diethylaminoethyl 6-chloro-a-methy1-91-I-carbazole-2-acetate.AcOH, diethylaminoethyl a-methy1-5H-[1]
benzopyrano[2,3-blpyridine-7-acetate.AcOH, diethylaminoethyl 2(4-chloropheny1)-a-methy1-5-benzoxazoleacetate.AcOH, diethylaminoethyl a-methy1-4-[(2-methyl-2-propenypaminolbenzeneacetate.AcOH, diethylaminoethyl 5-benzoyl-a-methyl-2-thiopheneacetate.AcOH, diethylaminoethyl 3-chloro-4-(2,5-dihydro-1H-pyrrol- 1-y1)-a-methyl benzeneacetate.AcOH, diethy-laminoethyl 2-(10, 11-dihydro-10-oxodibenzo(b,f)thiepin-2-yl)propionate.AcOH, di-ethylaminoethyl 248-methy1-10, 11-dihydro-11-oxodibenz(b,f)oxepin-2-yl)propionate.AcOH, diethylaminoethyl 2[4(2-oxocyclopentyl-methyl)phenylipropionate.AcOH, diethylaminoethyl 4-(1,3-dihydro-1-oxo-2H-isoindo1-2-y1)-a-methylbenzeneacetate.AcOH, diethy-laminoethyl a,3-dichloro-4-cyclohexylbenzeneacetate.AcOH, diethylaminoethyl 4,5-Dipheny1-2-oxazole propionate.AcOH, diethylaminoethyl 3(4-biphenylylcarbonyl)propionate.AcOH, diethylaminoethyl 5(4-chloropheny1)-beta-hydroxy-2-furanpropionate.AcOH, diethylaminoethyl 5-benzoy1-2,3-dihydro-1H-pyrrolizine-1-carboxylate.AcOH, diethylaminoethyl 6-chloro-5-cyclohexy1-2,3-dihydro-1H-indene-1-carboxylate.AcOH have shown analgesic activity nicely.

[17] The number of writhings that occurred when mice were administered an acetic acid solution intraperitoneally were counted, and the rate of inhibition based on the control group was calculated. diethylaminoethyl 2-(6-methoxy-2-naphthyl)propionate.AcOH
(100 mg/kg, B), diethylaminoethyl a-methy1-442-thienylcarbonyl)benzeneacetate.AcOH (100 mg/kg, C), diethylaminoethyl a-methyl(p-chlorobenzoy1)-5-methoxy-2-methylindole 3-acetate.AcOH (100 mg/kg, D), diethylaminoethyl 2-(2-fluoro-4-biphenylyl)propionate.AcOH (100 mg/kg, E), di-ethylaminoethyl 6-chloro-a-methyl-9H-carbazole-2-acetate.AcOH (100 mg/kg, F), di-ethylaminoethyl a-methyl-5H-[11benzopyrano[2,3-b]pyridine-7-acetate.AcOH (100 mg/kg, G), diethylaminoethyl 2(4-chloropheny1)-a-methy1-5-benzoxazoleacetate.AcOH (100 mg/kg, H), diethy-laminoethyl a-methyl-4-[(2-methyl-2-propenyl)aminolbenzeneacetate.AcOH (100 mg/
kg, I), diethylaminoethyl 5-benzoyl-a-methyl-2-thiopheneacetate.AcOH (100 mg/kg, J), diethylaminoethyl 3-chloro-4-(2,5-dihydro-1H-pyrrol-1-y1)-a-methyl benze-neacetate.AcOH (100 mg/kg, K), diethylaminoethyl 2-(10, 11-dihydro-10-oxodibenzo(b,f)thiepin-2-yl)propionate.AcOH (100 mg/kg, L), diethy-laminoethyl 248-methy1-10, 11-dihydro-11-oxodibenz(b,f)oxepin-2-yl)propionate.AcOH (100 mg/kg, M), diethy-laminoethyl 2[4(2-oxocyclopentyl-methyl)phenyllpropionate.AcOH (100 mg/kg, N), diethylaminoethyl 441,3-dihydro-l-oxo-2H-isoindo1-2-y1)-a-methylbenzeneacetate.AcOH (100 mg/kg, 0), diethylaminoethyl a,3-dichloro-4-cyclohexylbenzeneacetate.AcOH (100 mg/kg, P), diethylaminoethyl 4,5-Dipheny1-2-oxazole propionate.AcOH (100 mg/kg, Q), di-ethylaminoethyl 3(4-biphenylylcarbonyl)propionate.AcOH (100 mg,/kg, R), diethy-laminoethyl 5(4-chloropheny1)-beta-hydroxy-2-furanpropionate.AcOH (100 mg/kg, S), diethylaminoethyl 5-benzoy1-2,3-dihydro-1H-pyrrolizine-1-carboxylate.AcOH
(100 mg/kg, T), diethylaminoethyl 6-chloro-5-cyclohexy1-2,3-dihydro-1H-indene-1-carboxylate.AcOH (100 mg/kg, U) were administered transdermally the mice 30 minutes before the acetic acid solution was administered. The A group is the control group. The results are shown in Table 1.
Table 1. The rate of writhings inhibition by prodrugs of aryl- and het-eroarylpropionic acids

[18]
Group Dose (mg/kg) No. of Writhings %
A 0 35.0 -B 100 17.1 51 C 100 15.7 55 D 100 13.8 61 E 100 15.6 55 F 100 14.2 59 G 100 16.1 54 H 100 17.1 51 I 100 15.6 55 J 100 13.2 62 K 100 14.0 60 L 100 14.2 59 M 100 13.8 61 N 100 15.7 55 O 100 13.2 62 P 100 15.2 57 Q 100 15.7 55 R 100 14.2 59 S 100 15.6 55 T 100 16.1 54 U 100 15.2 57 The results show that the prodrugs demonstrate exceptional analgetic activity.
Other compounds of the general 'Structure l' or general 'Structure 2' show similar analgetic activity.

[19] Antipyretic activity: Rats received a sterilized E. coli suspension as a pyrogen. The control group is group A. 2 hours later, diethylaminoethyl 2-(6-methoxy-2-naphthyl)propionate.AcOH (100 mg/kg, B), diethylaminoethyl a-methyl-4-(2-thienylcarbonyl)benzeneacetate.AcOH (100 mg/kg, C), diethylaminoethyl a-methyl-(p-chlorobenzoy1)-5-methoxy-2-methylindole 3-acetate.AcOH (100 mg/kg, D), diethylaminoethyl 2-(2-fluoro-4-biphenylyl)propionate.AcOH (100 mg/kg, E), di-ethylaminoethyl 6-chloro-a-methyl-9H-carbazole-2-acetate.AcOH (100 mg/kg, F), di-ethylaminoethyl a-methyl-5H-[ llbenzopyrano[2,3-b]pyridine-7-acetate.AcOH (100 mg/kg, G), diethylaminoethyl 2-(4-chloropheny1)-a-methyl-5-benzoxazoleacetate.AcOH (100 mg/kg, H), diethy-laminoethyl a-methyl-4-[(2-methyl-2-propenyl)aminolbenzeneacetate.AcOH (100 mg/
kg, I), diethylaminoethyl 5-benzoyl-a-methyl-2-thiopheneacetate.AcOH (100 mg/kg, J), diethylaminoethyl 3-chloro-4-(2,5-dihydro-1H-pyrrol-1-y1)-a-methyl benze-neacetate.AcOH (100 mg/kg, K), diethylaminoethyl 2-(10, 11-dihydro-10-oxodibenzo(b,f)thiepin-2-yl)propionate.AcOH (100 mg/kg, L), diethy-laminoethyl 2-(8-methy1-10, 11-dihydro-11-oxodibenz(b,f)oxepin-2-yl)propionate.AcOH (100 mg/kg, M), diethy-laminoethyl 244-(2-oxocyclopentyl-methyl)phenyllpropionate.AcOH (100 mg/kg, N), diethylaminoethyl 4-(1,3-dihydro-1-oxo-2H-isoindo1-2-y1)-a-methylbenzeneacetate.AcOH (100 mg/kg, 0), diethylaminoethyl a,3-dichloro-4-cyclohexylbenzeneacetate.AcOH (100 mg/kg, P), diethylaminoethyl 4,5-Dipheny1-2-oxazole propionate.AcOH (100 mg/kg, Q), di-ethylaminoethyl 3-(4-biphenylylcarbonyl)propionate.AcOH (100 mg/kg, R), diethy-laminoethyl 5-(4-chloropheny1)-beta-hydroxy-2-furanpropionate.AcOH (100 mg/kg, S), diethylaminoethyl 5-benzoy1-2,3-dihydro-1H-pyffolizine-1-carboxylate.AcOH
(100 mg/kg, T), diethylaminoethyl 6-chloro-5-cyclohexy1-2,3-dihydro-1H-indene-1-carboxylate.AcOH (100 mg/kg, U) were administered transdermally. The body temperature of rats was taken at 90 min.
intervals before and after the administration of the test compounds. The results are shown in Table 2.
Table 2. Antipyretic Activity of prodrugs of aryl- and heteroarylpropionic acids.

[20]
Compound t=0 min. t=90 min. t=180 min. t=270 min.
A (Control 37.34 0.05 37.36 0.07 37.37 0.05 37.44 0.08 group) E (100mg/kg) 37.33 0.07 36.80 0.06 36.72 0.05 36.50 0.08 F (100mg/kg) 37.28 0.06 36.65 0.06 36.58 0.08 36.45 0.07 B (100mg/kg) 37.35 0.06 36.71 0.05 36.60 0.08 36.59 0.07 M (100mg/kg) 37.29 0.07 36.82 0.06 36.70 0.05 36.67 0.08 C (100mg/kg) 37.28 0.06 36.68 0.05 36.62 0.08 36.58 0.07 D (100mg/kg) 37.27 0.06 36.76 0.05 36.65 0.08 36.49 0.07 E (100mg/kg) 37.25 0.07 36.82 0.06 36.70 0.05 36.50 0.08 F (100mg/kg) 37.23 0.06 36.69 0.06 36.52 0.08 36.40 0.07 J (100mg/kg) 37.26 0.06 36.65 0.06 36.58 0.08 36.36 0.07 G (100mg/kg) 37.27 0.06 36.68 0.05 36.62 0.08 36.58 0.07 H (100mg/kg) 37.25 0.06 36.71 0.05 36.65 0.08 36.64 0.07 I (100mg/kg) 37.26 0.07 36.80 0.06 36.70 0.05 36.57 0.08 II (100mg/kg) 37.25 0.06 36.71 0.05 36.65 0.08 36.64 0.07 J (100mg/kg) 37.28 0.06 36.65 0.06 36.58 0.08 36.56 0.07 K (100mg/kg) 37.25 0.06 36.75 0.05 36.62 0.08 36.58 0.07 M (100mg/kg) 37.24 0.07 36.82 0.06 36.70 0.05 36.67 0.08 L (100mg/kg) 37.23 0.06 36.81 0.05 36.65 0.08 36.61 0.07 M (100mg/kg) 37.29 0.07 36.82 0.06 36.60 0.05 36.67 0.08 J (100mg/kg) 37.22 0.06 36.65 0.06 36.58 0.08 36.51 0.07 The results shown that the prodrugs demonstrated strong antipyretic activity at 100 mg/kg dose. Other compounds of the general 'Structure l' and general 'Structure 2' show similar antipyretic activity.

[21] Anti-inflammatory activity: diethylaminoethyl 2-(6-methoxy-2-naphthyl)propionate.AcOH (100 mg/kg, B), diethylaminoethyl a-methy1-442-thienylcarbonyl)benzeneacetate.AcOH (100 mg/kg, C), diethylaminoethyl a-methyl(p-chlorobenzoy1)-5-methoxy-2-methylindole 3-acetate.AcOH (100 mg/kg, D), diethylaminoethyl 2(2-fluoro-4-biphenylyl)propionate.AcOH (100 mg/kg, E), di-ethylaminoethyl 6-chloro-a-methyl-9H-carbazole-2-acetate.AcOH (100 mg/kg, F), di-ethylaminoethyl a-methyl-5H-[11benzopyrano[2,3-b]pyridine-7-acetate.AcOH (100 mg/kg, G), diethylaminoethyl 2(4-chloropheny1)-a-methy1-5-benzoxazoleacetate.AcOH (100 mg/kg, H), diethy-laminoethyl a-methyl-4-[(2-methyl-2-propenyl)aminolbenzeneacetate.AcOH (100 mg/
kg, I), diethylaminoethyl 5-benzoyl-a-methyl-2-thiopheneacetate.AcOH (100 mg/kg, J), diethylaminoethyl 3-chloro-4(2,5-dihydro-1H-pyrrol-1-y1)-a-methyl benze-neacetate.AcOH (100 mg/kg, K), diethylaminoethyl 2-(10, 11-dihydro-10-oxodibenzo(b,f)thiepin-2-yl)propionate.AcOH (100 mg,/kg, L), diethy-laminoethyl 248-methy1-10, 11-dihydro-11-oxodibenz(b,f)oxepin-2-yl)propionate.AcOH (100 mg/kg, M), diethy-laminoethyl 214-(2-oxocyclopentyl-methyl)phenyllpropionate.AcOH (100 mg/kg, N), diethylaminoethyl 4-(1,3-dihydro-1-oxo-2H-isoindo1-2-y1)-a-methylbenzeneacetate.AcOH (100 mg/kg, 0), diethylaminoethyl a,3-dichloro-4-cyclohexylbenzeneacetate.AcOH (100 mg/kg, P), diethylaminoethyl 4,5-Dipheny1-2-oxazole propionate.AcOH (100 mg/kg, Q), di-ethylaminoethyl 3-(4-biphenylylcarbonyl)propionate.AcOH (100 mg/kg, R), diethy-laminoethyl 5-(4-chloropheny1)-beta-hydroxy-2-furanpropionate.AcOH (100 mg/kg, S), diethylaminoethyl 5-benzoy1-2,3-dihydro-1H-pyffolizine-1-carboxylate.AcOH
(100 mg/kg, T), diethylaminoethyl 6-chloro-5-cyclohexy1-2,3-dihydro-1H-indene-1-carboxylate.AcOH (100 mg/kg, U) were administered transdermally. Group A is the controlled group. 60 minutes later, a carrageenin solution was administered subcutaneously to the foot pads of the rats. The volume of the hind paw was measured at every hour after the administration of the carrageenin, and the rate of increase in the volume of the paw was calculated and designated as the rate of swelling (%). The results obtained are shown in Figure 13, Figure 14, Figure 15, and Figure 16. The results show that these prodrugs by transdermal administration demonstrated good anti-inflammatory activity. Other compounds of the general 'Structure l' or general 'Structure 2' show similar anti-inflammatory activity.

[22] It is also known that a high oral dose of some of NSAIAs shows an anti-reactive-antiasthmatic activity by inhibition of the cyclooxygenase activity.
Due to their very high membrane penetration rate, these prodrugs can be used in treating asthma by spraying into the mouth or nose of the host.

[23] These prodrugs can also be used to treat psoriasis, acne, sunburn or other skin disorders due to their anti-inflammatory properties and very high skin penetration rate.

[24] The present invention relates to pharmaceutical preparations comprising of prodrugs of the general 'Structure l' or general 'Structure 2' in addition to customary auxiliaries and excipients, e.g. in the form of tablets, capsules or solutions for admin-istration orally and in the form of solutions, lotion, ointment, emulsion or gel for transdermal administration. The new active compounds of the general 'Structure 1' or general 'Structure 2'can be combined with vitamins such as A, B, C or E or beta-carotene, or other pharmaceuticals, such as folic acid, etc., for treating any NSAIAs-treatable conditions in humans or animals.

[25] Transdermal therapeutic application systems of compounds of the general' Structure l' or general 'Structure 2' or a composition comprising of at least one compound of the general 'Structure l' or general 'Structure 2' as an active ingredient, can be used for treating any NSAIAs-treatable conditions in humans or animals.
These systems can be a bandage or a patch comprising of one active substance-containing matrix layer and an impermeable backing layer. The most preferable system is an active substance reservoir, which has a permeable bottom facing the skin. By controlling the rate of release, this system enables NSAIAs to reach constantly optimal therapeutic blood levels to increase effectiveness and reduce the side effects of NSAIAs. These systems can be worn on the wrist, ankle, arm, leg, or any part of body.

[26] The compounds of the general formula (1) 'Structure l' or general formula (2) 'Structure 2' indicated above can be prepared from functional derivatives of aryl- and heteroarylpropionic acids, for example, acid halides or mixed anhydrides of the general formula (3) 'Structure 3' and general formula (4) 'Structure 4'.
Aryl 0 w 0 Structure 4 Structure 3 In structure 3 & 4, X represents halogen, alkoxycarbonyl or substituted aryloxy-carbonyloxy, Aryl, R, Y, Z, or W represent same groups as that are listed in 'structure l' or 'structure 2', by reaction with compounds of the general formula (5) 'Structure 5', H-X
I91) \pp \ 2 n Structure 5 In structure 5, R represents H, one of any alkyl, alkyloxy, alkenyl, or alkynyl residues having 1 to 12 carbon atoms, or aryl residues; R4 represents H, one of any alkyl, alkyloxy, alkenyl, or alkynyl residues having 1 to 12 carbon atoms, or aryl residues; X
represents 0, S or NH; and n=0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10

[27] The compounds of the general formula (1) 'Structure l' or general formula (2) 'Structure 2' indicated above can be prepared from naproxen, suprofen, a-methyl-(p-chlorobenzoy1)-5-methoxy-2-methylindole 3-acetic acid, flurbiprofen, carprofen, pranoprofen, benoxaprofen, alminoprofen, tiaprofenic acid, pirprofen, zaltoprofen, bermoprofen, loxoprofen, indoprofen, fenclorac, oxaprozin, fenbufen, orpanoxin, ketorolac, clidanac, and related compounds, by reaction with compounds of the general formula (5) 'Structure 5' by using coupling reagents, such as N,N'-Dicyclohexylcarbodiimide, N, N'-Diisopropylcarbodiimide, 0-(Benzotriazol-1-y1)-N,N,N',N'-tetramethyluronium tetrafluoroborate, 0-(Benzotriazol-1-y1)-N,N,N,N'-tetramethyluronium hexafluorophosphate, Benzotriazol-1-yl-oxy-tris (dimethylamino)phosphonium hexafluorophosphate, et al.

[28] When X represents 0, the compounds of the general formula (1) 'Structure 1' or general formula (2) 'Structure 2' indicated above can be prepared from metal salts or organic base salts of naproxen, suprofen, a-methyl-(p-chlorobenzoy1)-5-methoxy-2-methylindole 3-acetic acid, flurbiprofen, carprofen, pranoprofen, benoxaprofen, alminoprofen, tiaprofenic acid, pirprofen, zaltoprofen, bermoprofen, loxoprofen, indoprofen, fenclorac, oxaprozin, fenbufen, orpanoxin, ketorolac, clidanac, and related compounds, by reaction with compounds of the general formula (6) 'Structure 6'.
e = Z ,,4 6/

\-R :
Structure 6 In structure 6, R represents H, one of any alkyl, alkyloxy, alkenyl, or alkynyl residues having 1 to 12 carbon atoms, or aryl residues; R3 represents H, one of any alkyl, alkyloxy, alkenyl, or alkynyl residues having 1 to 12 carbon atoms, or aryl residues; R4 represents H, one of any alkyl, alkyloxy, alkenyl, or alkynyl residues having 1 to 12 carbon atoms, or aryl residues; Z represents halogen, or p-toluenesulphonyl, A-represents Cr, Br-, F, I-, Ac0-, citrate, or any negative ions; and n=0,1,2,3,4,5

[29] When X represents 0, the compounds of the general formula (1) 'Structure 1' or general formula (2) 'Structure 2' indicated above can be prepared from immobilized base salts of naproxen, suprofen, a-methyl-(p-chlorobenzoy1)-5-methoxy-2-methylindole 3-acetic acid, flurbiprofen, carprofen, pranoprofen, benoxaprofen, alminoprofen, tiaprofenic acid, pirprofen, zaltoprofen, bermoprofen, loxoprofen, indoprofen, fenclorac, oxaprozin, fenbufen, orpanoxin, ketorolac, clidanac, and related compounds of the general formula (7) 'Structure 7', HB
Aryl Structure 7 In structure 7, P represents cross-linked resin; Aryl represents aryl- and heteroaryl groups that are listed in 'structure l' and 'structure 2', B represents any base groups, such as pyridine, piperidine, triethylamine, or other base groups, by reaction with compounds of the general formula (6) 'Structure 6'.
Advantageous Effects [301 These pro-drugs of naproxen, suprofen, a-methyl-(p-chlorobenzoy1)-5-methoxy-2-methylindole 3-acetic acid, flurbiprofen, carprofen, pranoprofen, benoxaprofen, alminoprofen, tiaprofenic acid, pirprofen, zaltoprofen, bermoprofen, loxoprofen, indoprofen, fenclorac, oxaprozin, fenbufen, orpanoxin, ketorolac, clidanac, and related compounds have a lipophilic portion and a hydrophilic portion (the amine groups that exist in the protonated form at physiological pH). The positively charged amino groups of these pro-drugs have two major advantages. First, it largely increases the solubility of the drugs; when these new pro-drugs are administered orally in a dosage form such as a tablet, capsule, solution, or suspension, they will dissolve in gastric juice immediately. Second, the positive charge on the amino group of these pro-drugs will bond to the negative charge on the phosphate head group of membrane. Thus, the local concentration outside of the membrane will be very high and will facilitate the passage of these pro-drugs from a region of high concentration to a region of low concentration. When these pro-drugs enter the membrane, the hydrophilic part will push the pro-drugs into the cytosol, a semi-liquid concentrated aqueous solution or suspension. Due to the short stay in the GI tract, the pro-drugs will not cause gastric mucosal cell damage. Experiment results show that more than 90% of the pro-drugs were changed back to the drugs itself. The pro-drugs have a much better absorption rate, and thus the pro-drugs will have better strength than naproxen, suprofen, a-methyl-(p-chlorobenzoy1)-5-methoxy-2-methylindole 3-acetic acid, flurbiprofen, carprofen, pranoprofen, benoxaprofen, alminoprofen, tiaprofenic acid, pirprofen, zaltoprofen, bermoprofen, loxoprofen, indoprofen, fenclorac, oxaprozin, fenbufen, orpanoxin, ketorolac, clidanac, and related compounds at the same dosage. The experiment results suggest that the pro-drugs, diethylaminoethyl 2-(6-methoxy-2-naphthyl)propionate.AcOH, diethylaminoethyl a-methy1-442-thienylcarbonyl)benzeneacetate.AcOH, diethylaminoethyl a-methyl4p-chlorobenzoy1)-5-methoxy-2-methylindole 3-acetate.AcOH, diethy-laminoethyl 2-(2-fluoro-4-biphenylyl)propionate.AcOH, diethylaminoethyl 6-chloro-a-methyl-9H-carbazole-2-acetate.AcOH, diethylaminoethyl a-methy1-5H-[1]
benzopyrano[2,3-blpyridine-7-acetate.AcOH, diethylaminoethyl 2(4-chloropheny1)-a-methy1-5-benzoxazoleacetate.AcOH, diethylaminoethyl a-methy1-44(2-methyl-2-propenypaminolbenzeneacetate.AcOH, diethylaminoethyl 5-benzoyl-a-methyl-2-thiopheneacetate.AcOH, diethylaminoethyl 3-chloro-4-(2,5-dihydro-1H-pyrrol-1-y1)-a-methyl benzeneacetate.AcOH, diethy-laminoethyl 2-(10, 11-dihydro-10-oxodibenzo(b,f)thiepin-2-yl)propionate.AcOH, di-ethylaminoethyl 248-methy1-10, 11-dihydro-11-oxodibenz(b,f)oxepin-2-yl)propionate.AcOH, diethylaminoethyl 2[4(2-oxocyclopentyl-methyl)phenyllpropionate.AcOH, diethylaminoethyl 4-(1,3-dihydro-1-oxo-2H-isoindo1-2-y1)-a-methylbenzeneacetate.AcOH, diethy-laminoethyl a,3-dichloro-4-cyclohexylbenzeneacetate.AcOH, diethylaminoethyl 4,5-Dipheny1-2-oxazole propionate.AcOH, diethylaminoethyl 3(4-biphenylylcarbonyl)propionate.AcOH, diethylaminoethyl 5-(4-chloropheny1)-beta-hydroxy-2-furanpropionate.AcOH, diethylaminoethyl 5-benzoy1-2,3-dihydro-1H-pyrrolizine-1-carboxylate.AcOH, or diethylaminoethyl 6-chloro-5-cyclohexy1-2,3-dihydro-1H-indene-1-carboxylate.AcOH diffuses through human skin -100-130 times faster than does naproxen, suprofen, a-methyl4p-chlorobenzoy1)-5-methoxy-2-methylindole 3-acetic acid, flurbiprofen, carprofen, pranoprofen, benoxaprofen, alminoprofen, tiaprofenic acid, pirprofen, zaltoprofen, bermoprofen, loxoprofen, indoprofen, fenclorac, oxaprozin, fenbufen, orpanoxin, ketorolac, or clidanac, and related compounds. It takes 2-4 hours for naproxen, suprofen, a-methyl(p-chlorobenzoy1)-5-methoxy-2-methylindole 3-acetic acid, flurbiprofen, carprofen, pranoprofen, benoxaprofen, alminoprofen, tiaprofenic acid, pirprofen, zaltoprofen, bermoprofen, loxoprofen, indoprofen, fenclorac, oxaprozin, fenbufen, orpanoxin, ketorolac, or clidanac, and related compounds to reach the peak plasma level when they are taken orally, but these prodrugs only took about 40-50 minutes to reach the peak plasma level. The most exciting result is that the pro-drugs can be administered not only orally, but also transdermally for any type of medical treatment and should avoid most of the side effects of naproxen, suprofen, a-methyl4p-chlorobenzoy1)-5-methoxy-2-methylindole 3-acetic acid, flurbiprofen, carprofen, pranoprofen, benoxaprofen, alminoprofen, tiaprofenic acid, pirprofen, zaltoprofen, bermoprofen, loxoprofen, indoprofen, fenclorac, oxaprozin, fenbufen, orpanoxin, ketorolac, or clidanac, and related compounds, most notably GI dis-turbances such as dyspepsia, gastroduodenal bleeding, gastric ulcerations, gastritis, and renal toxicity. Another great benefit of transdermal administration of these pro-drugs is that administering medication, especially to children, will be much easier.
Description of Drawings [31] Figure 1: Cumulative amounts of diethylaminoethyl 2-(6-methoxy-2-naphthyl)propionate.AcOH (A, 30% solution), diethylaminoethyl a-methy1-442-thienylcarbonyl)benzeneacetate.AcOH (B, 30% solution), diethy-laminoethyl a-methyl(p-chlorobenzoy1)-5-methoxy-2-methylindole 3-acetate.AcOH
(C, 30% solution), diethylaminoethyl 2-(2-fluoro-4-biphenylyl)propionate.AcOH
(D,

30% solution), diethylaminoethyl 6-chloro-a-methyl-9H-carbazole-2-acetate.AcOH

(E, 30% solution), naproxen (F, 30% suspension), suprofen (G, 30% suspension), a-methyl4p-chlorobenzoy1)-5-methoxy-2-methylindole 3-acetic acid (H, 30%
suspension), flurbiprofen (I, 30% suspension), or carprofen (J, 30%
suspension) crossing isolated human skin tissue in Franz cells (n=5). In each case, the vehicle was pH 7.4 phosphate buffer (0.2 M).
[32] Figure 2: Cumulative amounts of diethylaminoethyl a-methyl-5H-[1]
benzopyrano[2,3-b]pyridine-7-acetate.AcOH (A, 30% solution), diethylaminoethyl 2(4-chloropheny1)-a-methy1-5-benzoxazoleacetate.AcOH (B, 30% solution), diethy-laminoethyl a-methyl-4-[(2-methyl-2-propenyl)aminolbenzeneacetate.AcOH (C, 30%

solution), diethylaminoethyl 5-benzoyl-a-methyl-2-thiopheneacetate.AcOH (D, 30%
solution), diethylaminoethyl 3-chloro-4(2,5-dihydro-1H-pyrrol-1-y1)-a-methyl benze-neacetate.AcOH (E, 30% solution), pranoprofen (F, 30% suspension), benoxaprofen (G, 30% suspension), alminoprofen (H, 30% suspension), tiaprofenic acid (I, 30%
suspension), or pirprofen (J, 30% suspension) crossing isolated human skin tissue in Franz cells (n=5). In each case, the vehicle was pH 7.4 phosphate buffer (0.2 M).
[33] Figure 3: Cumulative amounts of diethylaminoethyl 2-(10, 11-dihydro-10-oxodibenzo(b,f)thiepin-2-yl)propionate.AcOH (A, 30% solution), di-ethylaminoethyl 248-methy1-10, 11-dihydro-11-oxodibenz(b,f)oxepin-2-yl)propionate.AcOH (B, 30% solution), diethy-laminoethyl 2[4(2-oxocyclopentyl-methyl)phenyllpropionate.AcOH (C, 30%
solution), diethylaminoethyl 4-(1,3-dihydro-1-oxo-2H-isoindo1-2-y1)-a-methylbenzeneacetate.AcOH (D, 30%
solution), diethylaminoethyla,3-dichloro-4-cyclohexylbenzeneacetate.AcOH (E, 30%
solution), zaltoprofen (F, 30% suspension), bermoprofen (G, 30% suspension), loxoprofen (II, 30% suspension), indoprofen (I, 30% suspension), or fenclorac (J, 30%
suspension) crossing isolated human skin tissue in Franz cells (n=5). In each case, the vehicle was pH 7.4 phosphate buffer (0.2 M).

[34] Figure 4: Cumulative amounts of diethylaminoethyl 4,5-Dipheny1-2-oxazole propionate.AcOH (A, 30% solution), diethylaminoethyl 3(4-biphenylylcarbonyl)propionate.AcOH (B, 30% solution), diethylaminoethyl 5(4-chloropheny1)-beta-hydroxy-2-furanpropionate.AcOH (C, 30% solution), diethy-laminoethyl 5-benzoy1-2,3-dihydro-1H-pyrrolizine-1-carboxylate.AcOH (D, 30%
solution), diethylaminoethyl 6-chloro-5-cyclohexy1-2,3-dihydro-1H-indene-1-carboxylate.AcOH (E, 30%
solution), oxaprozin (F, 30% suspension), fenbufen (G, 30% suspension), orparioxin (11, 30%
suspension), ketorolac (I, 30% suspension), or clidanac (J, 30% suspension) crossing isolated human skin tissue in Franz cells (n=5). In each case, the vehicle was pH 7.4 phosphate buffer (0.2 M).
[35] Figure 5: Total plasma levels of naproxen, suprofen, a-methyl4p-chlorobenzoy1)-5-methoxy-2-methylindole 3-acetic acid, flurbiprofen, carprofen after topical application of 1 ml of a 20% solution of diethylaminoethyl 2-(6-methoxy-2-naphthyl)propionate.AcOH (A), diethylaminoethyl a-methy1-442-thienylcarbonyl)benzeneacetate.AcOH (B), diethylaminoethyl a-methyl4p-chlorobenzoy1)-5-methoxy-2-methylindole 3-acetate.AcOH (C), diethy-laminoethyl 2-(2-fluoro-4-biphenylyl)propionate.AcOH (D), diethylaminoethyl 6-chloro-a-methyl-9H-carbazole-2-acetate.AcOH (E), naproxen (F) , suprofen (G), a-methyl4p-chlorobenzoy1)-5-methoxy-2-methylindole 3-acetic acid (H), flurbiprofen (I), or caiprofen (J) in isopropanol to the backs of hairless mice (n=5).
[36] Figure 6: Total plasma levels of pranoprofen, benoxaprofen, alminoprofen, tiaprofenic acid, or pliprofen after topical application of diethylaminoethyl a-methy1-5H-[1]benzopyrano[2,3-blpyridine-7-acetate.AcOH (A), diethylaminoethyl 2(4-chloropheny1)-a-methy1-5-benzoxazoleacetate.AcOH (B), diethylaminoethyl a-methy1-4-[(2-methyl-2-propenypaminolbenzeneacetate.AcOH (C), diethylaminoethyl 5-benzoyl-a-methyl-2-thiopheneacetate.AcOH (D), diethylaminoethyl 3-chloro-4-(2,5-dihydro-1H-pyrrol-1-y1)-a-methyl benzeneacetate.AcOH (E), pranoprofen (F), benoxaprofen (G), alminoprofen (H), tiaprofenic acid (I), or pirprofen (J) 1 ml of a 20% solution of in isopropanol to the backs of hairless mice (n=5).
[37] Figure 7: Total plasma levels of zaltoprofen, bermoprofen, loxoprofen, indoprofen, fenclorac after topical application of diethylaminoethyl 2-(10, 11-dihydro-10-oxodibenzo(b,f)thiepin-2-yl)propionate.AcOH (A), diethylaminoethyl 248-methy1-10, 11-dihydro-11-oxodibenz(b,floxepin-2-yl)propionate.AcOH (B), di-ethylaminoethyl 2[4(2-oxocyclopentyl-methyl)phenyllpropionate.AcOH (C), diethy-laminoethyl 441,3-dihydro-1-oxo-211-isoindo1-2-y1)-a-methylbenzeneacetate.AcOH

(D), diethylaminoethyla,3-dichloro-4-cyclohexylbenzeneacetate.AcOH (E), zahoprofen (F), bermoprofen (G), loxoprofen (H), indoprofen (I), fenclorac (J) 1 ml of a 20% solution of in isopropanol to the backs of hairless mice (n=5).
[381 Figure 8: Total plasma levels of oxaprozin, fenbufen, oipanoxin, ketorolac, and clidanac after topical application of diethylaminoethyl 4,5-Dipheny1-2-oxazole propionate.AcOH (A), diethylaminoethyl 3(4-biphenylylcarbonyl)propionate.AcOH
(B), diethylaminoethyl 5(4-chloropheny1)-beta-hydroxy-2-furanpropionate.AcOH
(C), diethylaminoethyl 5-benzoy1-2,3-dihydro-1H-pyrrolizine-1-carboxylate.AcOH (D), di-ethylaminoethyl 6-chloro-5-cyclohexy1-2,3-dihydro-1H-indene-1-carboxylate.AcOH

(E), oxaprozin (F), fenbufen (G), orpanoxin (H), ketorolac (I), or clidariac (J)1 ml of a 20% solution of in isopropanol to the backs of hairless mice (n=5).
[391 Figure 9: The prolongation time of the pain threshold of mice tails after 50mg/kg of diethylaminoethyl 2-(6-methoxy-2-naphthyl)propionate.AcOH (B), diethylaminoethyl a-methyl-4(2-thienylcarbonyl)benzeneacetate.AcOH (C), diethylaminoethyl a-methyl4p-chlorobenzoy1)-5-methoxy-2-methylindole 3-acetate.AcOH (D), diethy-laminoethyl 2-(2-fluoro-4-biphenylyl)propionate.AcOH (E), diethylaminoethyl 6-chloro-a-methyl-9H-carbazole-2-acetate.AcOH (F) were administered transdermally.
Group A is the control group.
[401 Figure 10: The prolongation time of the pain threshold of mice tails after 50mg/kg of diethylaminoethyl a-methyl-5H-[11benzopyrano[2,3-blpyridine-7-acetate.AcOH
(G), diethylaminoethyl 2(4-chloropheny1)-a-methy1-5-benzoxazoleacetate.AcOH
(H), diethylaminoethyl a-methyl-4-[(2-methyl-2-propenypamino]benzeneacetate.AcOH
(I), diethylaminoethyl 5-benzoyl-a-methyl-2-thiopheneacetate.AcOH (J), diethy-laminoethyl 3-chloro-4(2,5-dihydro-1H-pyrrol-1-y1)-a-methyl benzeneacetate.AcOH
(K) were administered transdermally. Group A is the control group.
[411 Figure 11: The prolongation time of the pain threshold of mice tails after 50mg/kg of diethylaminoethyl 2-(10, 11-dihydro-10-oxodibenzo(b,f)thiepin-2-yl)propionate.AcOH (L), diethylaminoethyl 248-methyl- 10, 11-dihydro-11-oxodibenz(b,floxepin-2-y1)propionate.AcOH (M), di-ethylaminoethyl 2[4(2-oxocyclopentyl-methyl)phenyllpropionate.AcOH (N), diethy-laminoethyl 441,3-dihydro-1-oxo-211-isoindo1-2-y1)-a-methylbenzeneacetate.AcOH

(0), diethylaminoethyl a,3-dichloro-4-cyclohexylbenzeneacetate.AcOH (P), were ad-ministered transdermally. Group A is the control group.
[421 Figure 12: The prolongation time of the pain threshold of mice tails after 50mg/kg of diethylaminoethyl 4,5-Dipheny1-2-oxazole propionate.AcOH (Q), diethylaminoethyl 3(4-biphenylylcarbonyl)propionate.AcOH (R), diethylaminoethyl 5(4-chloropheny1)-beta-hydroxy-2-furanpropionate.Ac011 (S), diethylaminoethyl 5-benzoy1-2,3-dihydro-1H-pyrrolizine-1-carboxylate.AcOH (T), diethylaminoethyl 6-chloro-5-cyclohexy1-2,3-dihydro-1H-indene-1-carboxylate.AcOH (U) were ad-ministered transdermally. Group A is the control group.

[43] Figure 13. The rate of swelling (%) after a carrageenin injection. 1 Hour before the carrageenin injection, diethylaminoethyl 2-(6-methoxy-2-naphthyl)propionate.AcOH
(100 mg/kg, B), diethylaminoethyl a-methy1-4-(2-thienylcarbonyl)benzeneacetate.AcOH (100 mg/kg, C), diethylaminoethyl a-methyl-(p-chlorobenzoy1)-5-methoxy-2-methylindole 3-acetate.AcOH (100 mg/kg, D), diethylaminoethyl 2-(2-fluoro-4-biphenylyl)propionate.AcOH (100 mg/kg, E), di-ethylaminoethyl 6-chloro-a-methyl-9H-carbazole-2-acetate.AcOH (100 mg/kg, F) were administered transdermally. A group is the control group.
[44] Figure 14. The rate of swelling (%) after a carrageenin injection. 1 Hour before the carrageenin injection, diethylaminoethyl a-methyl-5H-Mbenzopyrano[2,3-b]
pyfidine-7-acetate.AcOH (100 mg/kg, G), diethylaminoethyl 2-(4-chloropheny1)-a-methyl-5-benzoxazoleacetate.AcOH (100 mg/kg, H), diethy-laminoethyl a-methyl-4-[(2-methyl-2-propenyl)aminolbenzeneacetate.AcOH (100 mg,/
kg, I), diethylaminoethyl 5-benzoyl-a-methyl-2-thiopheneacetate.AcOH (100 mg/kg, J), diethylaminoethyl 3-chloro-4-(2,5-dihydro-1H-pyrrol-1-y1)-a-methyl benze-neacetate.AcOH (100 mg/kg, K) were administered transdermally. Group A is the control group.
[45] Figure 15. The rate of swelling (%) after a carrageenin injection. 1 Hour before the carrageenin injection, diethylaminoethyl 2-(10, 11-dihydro-10-oxodibenzo(b,f)thiepin-2-yl)propionate.AcOH (100 mg/kg, L), diethy-laminoethyl 2-(8-methy1-10, 11-dihydro-11-oxodibenz(b,f)oxepin-2-yl)propionate.AcOH (100 mg/kg, M), diethy-laminoethyl 214-(2-oxocyclopentyl-methyl)phenyllpropionate.AcOH (100 mg/kg, N), diethylaminoethyl 4-(1,3-dihydro-1-oxo-2H-isoindo1-2-y1)-a-methylbenz eneacetate.AcOH (100 mg/kg, 0), diethylaminoethyl a,3-dichloro-4-cyclohexylbenzeneacetate.AcOH (100 mg/kg, P) were administered transdermally. Group A is the control group.
[46] Figure 16. The rate of swelling (%) after a carrageenin injection. 1 Hour before the carrageenin injection, diethylaminoethyl 4,5-Dipheny1-2-oxazole propionate.AcOH
(100 mg/kg, Q), diethylaminoethyl 3-(4-biphenylylcarbonyl)propionate.Ac0H (100 mg/kg, R), diethylaminoethyl 5-(4-chloropheny1)-beta-hydroxy-2-furanpropionate.AcOH (100 mg/kg, S), diethy-laminoethyl 5-benzoy1-2,3-dihydro-1H-pyrrolizine-1-carboxylate.AcOH (100 mg/kg, T), diethylaminoethyl 6-chloro-5-cyclohexy1-2,3-dihydro-1H-indene-1-carboxylate.AcOH (100 mg/kg, U) were administered transdermally. Group A is the control group.
[47] Figure 17. In structure 1, R represents CU, OH, Cl, F, or Br; Ri represents H, one of any alkyl, alkyloxyl, alkenyl or alkynyl residues having 1 to 12 carbon atoms, or aryl residues; R2 represents H, one of any alkyl, alkyloxy, alkenyl or alkynyl residues having 1 to 12 carbon atoms, or aryl residues; R3 represents H, one of any alkyl, alkyloxy, alkenyl or alkynyl residues having 1 to 12 carbon atoms, or aryl residues; X
represents 0, S, NH, OCH2C00, OCH2COS, or OCH2CONH; A- represents Cl, Br, F
, I, Ac0-, citrate, or any negative ions; and n=0,1,2,3,4,5,6,7,8,9,10 ;
Aryl represents aryl- and heteroaryl groups [48] Figure 18. In structure 2, W represents H, OH, Cl, F, or Br; Ri represents H, one of any alkyl, alkyloxyl, alkenyl or alkynyl residues having 1 to 12 carbon atoms, or aryl residues; R2 represents H, one of any alkyl, alkyloxy, alkenyl or alkynyl residues having 1 to 12 carbon atoms, or aryl residues; R3 represents H, one of any alkyl, alkyloxy, alkenyl or alkynyl residues having 1 to 12 carbon atoms, or aryl residues; X
represents 0, S, NH, OCH2C00, OCH2COS, or OCH2CONH; A- represents Cl, Br, F
, I, Ac0-, citrate, or any negative ions; and n=0,1,2,3,4,5,6,7,8,9,10 ; Y
or Y and Z
together represent aryl- and heteroaryl groups.
Best Mode Preparation of diethylaminoethyl 2-(6-methoxy-2-naphthyl)propionate.AcOH
[49] 11.7 g (0.1 mol) of diethylaminoethanol was dissolved in 10% sodium bicarbonate (200 ml) and acetone (100 ml). 24.9 g (0.1 mol) of 2-(6-methoxy-2-naphthyl) propionyl chloride was added into the reaction mixture. The mixture is stirred for 3 hours at RT. The solvents are evaporated off. The residue is suspended in ethyl acetate (500m1). 5% sodium bicarbonate (200 ml) is added into the reaction mixture with stiffing. Ethyl acetate layer is collected and washed with water (3 x 500 ml).
The ethyl acetate solution was dried over anhydrous sodium sulfate. Sodium sulfate is removed by filtration. 6 g of acetic acid is added into the reaction mixture with stirring. The organic solution was evaporated off. After drying, it yielded 36 g of the desired product (89.9 %). Hygroscopic product; Solubility in water: 350 mg/ml;
Elementary analysis: C221131N05; MW: 389.49. Calculated % C: 67.84; H: 8.02; N: 3.60; 0:
20.54;
Found % C: 67.82; H: 8.04; N: 3.58; 0: 20.56. 1H-NMR (400 MHz, DO): 6: 1.36 (t, 6H), 1.50 (d, 3H), 2.11 (s, 3H), 3.20 (m, 4H), 3.47(m, 2H), 3.70 (s, 3H), 3.78 (m, 1H), 4.48 (t, 2H), 6.88 (b, 1H), 6.98 (s, 1H), 7.03 (d, 1H), 7.18 (d, 111), 7.43 (s, 1H), 7.50 (d, 1H), 7.54 (d, 1H).
Mode for Invention Preparation of diethylaminoethyl a-methy1-4-(2-thieny1carbony1) benze-neacetate.AcOH.
[50] 28.1 g (0.1 mol) of a-methyl-4-(2-thienylcarbonyl) benzeneacetyl chloride was dissolved in 100 ml of chloroform. The mixture was cooled to 0 C. 15 ml of tri-ethylamine and 11.7 g (0.1 mol) of diethylaminoethanol were added into the reaction mixture. The mixture is stirred for 3 hours at RT. The solvents are evaporated off. The residue is dissolved in methanol (300m1), 5% sodium bicarbonate (200 ml) is added into the reaction mixture. The mixture is stiffed for 3 hr. The mixture is evaporated to dryness. Methanol (300 ml) is added into the residue with stirring. Solid is removed by filtration and washed with methanol. The solution is evaporated to dryness and the residue is dissolved in chloroform (200 ml). 6 g of acetic acid is added into the reaction mixture with stirring. Some solid is removed by filtration. Another 6 g of acetic acid is added into the reaction mixture with stirring. The organic solution was evaporated off.
After drying, it yielded 35 g of the desired product (83.2%). Hygroscopic product;
Solubility in water: 400 mg/ml; Elementary analysis: C22H3iNO5S; MW: 419.53.
Calculated % C: 62.68; H: 7.41; N: 3.32; 0: 18.98; S: 7.61; Found % C: 62.63;
H:
7.45; N: 3.31; 0: 19.01; S: 7.60. 1H-N4R (400 MHz, DO): 8: 1.36 (t, 6H), 1.45 (d, 3H), 2.11 (s, 3H), 3.20 (m, 411), 3.47(m, 211), 3.78 (m, 1H), 4.48 (t, 2H), 6.88 (b, 1H), 6.98 (s, 111), 7.31 (d, 2H), 7.05 (m, 1H), 7.43 (m, 211), 7.70 (d, 211).
Preparation of S-diethylarninoethyl 2-(2-fluoro-4-biphenylyl)propionate.AcOH
[51] 13.2 g (0.1 mol) of diethylaminoethyl mercaptan was dissolved in 10%
sodium bi-carbonate (200 ml) and acetone (100 ml). 26.3 g (0.1 mol) of 2-(2-fluoro-4-biphenyly1) propionyl chloride was added into the reaction mixture. The mixture is stirred for 3 hours at RT. The solvents are evaporated off. The residue is suspended in ethyl acetate (500m1). 5% sodium bicarbonate (200 ml) is added into the reaction mixture with stirring. Ethyl acetate layer is collected and washed with water (3 x 500 ml).
The ethyl acetate solution was dried over anhydrous sodium sulfate. Sodium sulfate is removed by filtration. 6 g of acetic acid is added into the reaction mixture with stirring. The organic solution was evaporated off. After drying, it yielded 36 g of the desired product (85.8%). Hygroscopic product; Solubility in water: 400 mg/ml;
Elementary analysis: C231130FNO3S; MW: 419.55. Calculated % C: 65.84; H: 7.21; F: 4.53;
N:
3.34; 0: 11.44; S: 7.64. Found % C: 65.80; H: 7.23; F: 4.55; N: 3.32, 0:
11.47; S:
7.63. 111-NMR (400 MHz, D20): 8: 1.35 (t, 611), 1.44 (d, 311), 2.11 (s, 311), 3.20 (m, 4H), 3.30(t, 2H), 3.80 (m, 111), 3.88 (t, 2H), 6.88 (b, 111), 6.88 (m, 1H), 6.95 (m, 1H), 7.22 (m, 111), 7.32 (m, 211), 7.41 (m, 111), 7.48 (m, 211).
Preparation of N-diethylaminoethyl 5-benzoy1-2, 3-dihydro-1H-pyrrolizine-1-carboxylarnide.AcOH.
[521 11.6 g (0.1 mol) of diethylaminoethylamine was dissolved in 10%
sodium bi-carbonate (200 ml) and acetone (100 ml). 27.4 g (0.1 mol) of 5-benzoy1-2, 3-dihydro-1H-pyrrolizine-1-carboxyly1 chloride was added into the reaction mixture.

31 The mixture is stirred for 3 hours at RT. The solvents are evaporated off. The residue is suspended in ethyl acetate (500m1). 5% sodium bicarbonate (200 ml) is added into the reaction mixture with stirring. Ethyl acetate layer is collected and washed with water (3 x 500 m1). The ethyl acetate solution was dried over anhydrous sodium sulfate.
Sodium sulfate is removed by filtration. 6 g of acetic acid is added into the reaction mixture with stirring. The organic solution was evaporated off. After drying, it yielded 35 g of the desired product (84.8 %). Hygroscopic product; Solubility in water: 400 metril;
Elementary analysis: C.H31N304; MW: 412.50. Calculated % C: 66.81; H: 7.56; N:

10.16; 0: 15.48; Found % C: 66.90; H: 7.38; N: 10.18; 0: 15.54. 'H-NIV1R (400 MHz, DO): 8: 1.39 (t, 611), 2.10 (s, 311), 2.27 (m, 211), 3.22 (in, 411), 3.50(t, 211), 3.60 (t, 211), 3.80 (m, 211), 3.71 (in, 111), 5.85 (m, 111), 6.70 (m, 1H), 6.85 (b, 1H), 7.32 (b, 1H), 7.40 (m, 1H), 7.45 (in, 211), 7.78 (m, 211).
Preparation of N-diethylairninoethyl 4, 5-Dipheny1-2-oxazole pro-pionamideAcOH
[53] 29.3 g (0.1 mol) of 4, 5-Dipheny1-2-oxazole propionic acid was dissolved in 100 ml of acetonitrile. 32.1 g of 0-(Benzotriazol-1-371)-N,N,N,N-tetramethyluronium tetraflu-oroborate and 30 ml of triethylamine were added into the reaction mixture.
11.6 g of diethylaminoethylamine was added into the reaction mixture. The mixture was stirred for 3 hours at RT. The solvents were evaporated off. 250 ml of ethyl acetate was added into the reaction mixture and the mixture was washed with water (3 x 100 ml).
The organic solution was dried over anhydrous sodium sulfate. Sodium sulfate was removed by filtration. 6 g of acetic acid was added into the reaction mixture with stirring. Hexane (200 ml) was added. The solid product was collected by filtration.
After drying, it yielded 40 g of the desired product (88.6%). Hygroscopic product;
Solubility in water: 400 mg/ml; Elementary analysis: C26H33N304; MW: 451.56.
Calculated % C: 69.16; 11: 7.37; N: 9.31; 0: 14.17; Found % C: 69.11; H: 7.40;
N:
9.30; 0: 14.19. 'H-NMR (400 MHz, DO): 8: 1.41 (t, 61), 2.10 (s, 311), 2.45 (t, 211), 2.76 (t, 211), 3.22 (m, 411), 3.49(t, 211), 3.60 (t, 211), 6.87 (b, 111), 7.22 (b, 111), 7.22 (in, 211), 7.32 (m, 4H), 7.47 (m, 411).
Preparation of diethylarninoethyl 6-ehloro-a-methyl-911-earbazo1e-2-acetate.AcOH.
[54] 60 g of Polymer-bound triethylamine (3 mol/g, 100-200 mesh) was suspended in 180 ml of chloroform. 27.4 g (0.1 mol) of 6-chloro-a-methy1-9H-carbazole-2-acetic acid, was added into the mixture with stirring. 43 g (0.15niol) of diethylaminoethyl bromide.HBr was added into the mixture and the mixture was stirred for 5 hours at RT.
The polymer was removed by filtration and washed with tetrahydrofuran (3 x 50 m1).
8.2 g (0.1 mol) of sodium acetate was added into the reaction mixture with stirring, =

32 The mixture was stirred for 2 h. The solid was removed by filtration and washed with chloroform (3 x 50 ml). The solution was concentrated in vacuo to 100 ml. Then ml of hexane was added into the solution. The solid product was collected by filtration and washed with hexane (3 x 100 ml). After drying, it yielded 38 g of the desired product (87.8%). Hygroscopic product; Solubility in water: 400 mg/m1;
Elementary analysis: C231129C1N204; MW: 432.94. Calculated % C: 63.81; 11: 6.75; Cl:
8.19, N:
6.47; 0: 14.78; Found % C: 63.85; H: 6.78; Cl: 8.17; N: 6.44; 0: 14.76. 'H-NMR
(400 MHz, DO): 6: 1.39 (t, 611), 1.47 (d, 3H), 2.11 (s, 311), 3.21 (m, 4H), 3.49(m, 2H), 3.77 (m, 111), 4.48 (t, 211), 6.80 (b, 111), 6.85 (m, 111), 7.10 (m, 111), 7.05 (m, 11-1), 7.26 (m, 11-1), 7.34 (m, 111), 7.50 (m, 111), 7.52 (m, 1H).
Industrial Applicability [55] The pro-drugs of the general formula (1) 'Structure l' and general formula (2) 'Structure 2' are superior to naproxen, suprofen, a-methyl-(p-chlorobenzoy1)-5-methoxy-2-methylindole 3-acetic acid, flurbiprofen, carprofen, pranoprofen, benoxaprofen, alminoprofen, tiaprofenic acid, pirprofen, zaltoprofen, bermoprofen, loxoprofen, indoprofen, fenclorac, oxaprozin, fenbufen, orpanoxin, ketorolac, or clidanac, and related compounds. They may be used medicinally in treating any naproxen, suprofen, a-methyl-(p-chlorobenzoyI)-5-methoxy-2-methylindole 3-acetic acid, flurbiprofen, carprofen, pranoprofen, benoxaprofen, ahninoprofen, tiaprofenic acid, pirprofen, zahoprofen, bermoprofen, loxoprofen, indoprofen, fenclorac, oxaprozin, fenbufen, orpanoxin, ketorolac, clidanac, and related compounds-treatable conditions in humans or animals. They may be used for the relief of signs and symptoms of rheumatoid arthritis and osteoarthritis, the reduction of fever, and the treatment of dysinenorrhea.
They may be also prescribed for diabetic neuropathy and acute migraine headache.
Due to their very high membrane penetration rate, these pro-drugs can be used in treating asthma by inhalation to a host. They can be used to treat psoriasis, acne, sunburn or other skin disorders due to their anti-inflammatory properties.
[561

Claims (63)

CLAIMS:

1. A compound of the general formula (1) wherein R represents CH3, OH, Cl, F, or Br; R1 represents H, alkyl, alkyloxyl, alkenyl or alkynyl residues having 1 to 12 carbon atoms, or aryl residues; R2 represents H, alkyl, alkyloxy, alkenyl or alkynyl residues having 1 to 12 carbon atoms, or aryl residues; R3 represents H; X represents O, S, NH, OCH2COO, OCH2COS, or OCH2CONH; A-represents a negative ion; n is 0, 1, 2, 3, 4, 5, 6, 7, 8, 9 or 10; and Aryl represents:
wherein X represents CI, F. CH3S, or CHF2O, wherein Y represents CH3O, F, CH3CO, (CH3)2N, CH3, or CH2=CH-CH2, X represents CI, F, CF3, CH3SO, or CH3S, and R represents CH3, C2H5, or C3H7, wherein X represents CI, wherein X represents Cl, Br, F, or CH3.
wherein X represents CI, Br, F, or CH3, wherein X represents CI, F, or Br, wherein X represents CO or O, wherein X represents Cl, Br, F, or CH3O, wherein X represents O or S, Y represents CH2 or CO, Z represents CO or CH2, and R represents H, CH3, or C2H5,

2. A compound of the general formula (2):
wherein W represents H, OH, CI, F, or Br; R1 represents H, alkyl, alkyloxyl, alkenyl or alkynyl residues having 1 to 12 carbon atoms, or aryl residues; R2 represents H, alkyl, alkyloxy, alkenyl or alkynyl residues having 1 to 12 carbon atoms, or aryl residues; R3 represents H; X represents O, S, NH, OCH2COO, OCH2COS, or OCH2CONH; A-represents a negative ion; n is 0, 1, 2, 3, 4, 5, 6, 7, 8, 9 or 10, Y represents H; and Z
represents:
wherein X represents Cl, F, or Br, or or W represents H, and Z and Y together represent:
wherein X represents Cl, F, or Br,

3. The compound according to claim 1 or 2. wherein N represents CI, Br-, F-, I-, AcO- or citrate.

4. A process for the preparation of the compound of claim 1 or claim 2, wherein a functional derivative of naproxen, suprofen, .alpha.-methyl-(p-chlorobenzoyl)-5-methoxy-2-methylindole 3-acetic acid, flurbiprofen, carprofen, pranoprofen, benoxaprofen, alminoprofen, tiaprofenic acid, pirprofen, zaltoprofen, bermoprofen, loxoprofen, indoprofen, fenclorac, oxaprozin, fenbufen, orpanoxin, ketorolac, clidanac, or a related compound thereof, is reacted with a compound of the general formula (5):
wherein R3 represents H, alkyl, alkyloxy, alkenyl, or alkynyl residues having 1 to 12 carbon atoms, or aryl residues; R4 represents H, alkyl, alkyloxy, alkenyl, or alkynyl residues having 1 to 12 carbon atoms, or aryl residues; X represents O, S, NH, OCH2COO, OCH2COS, or OCH2CONH; and n is 0, 1, 2, 3, 4, 5, 6, 7, 8, 9 or 10.

5. The process according to claim 4, wherein the related compound is a halide or a mixed anhydride.

6. A process for the preparation of the compound of claim 1 or claim 2, wherein naproxen, suprofen, .alpha.-methyl-(p-chlorobenzoyl)-5-methoxy-2-methylindole 3-acetic acid, flurbiprofen, carprofen, pranoprofen, benoxaprofen, alminoprofen, tiaprofenic acid, pirprofen, zaltoprofen, bermoprofen, loxoprofen, indoprofen, fenclorac, oxaprozin, fenbufen, orpanoxin, ketorolac, clidanac, or a related compound thereof, is reacted with a compound of the general formula (5) as defined in claim 5 by using a coupling reagent.

7. The process according to claim 6, wherein the coupling reagent is N,N'-Dicyclohexylcarbodiimide, N,N'-Diisopropylcarbodiimide, O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate, O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate, or Benzotriazol-1-yl-oxy-tris (dimethylamino)phosphonium hexafluorophosphate.

8. A process for the preparation of the compound of claim 1 or claim 2, wherein a metal salt, organic base salt, or immobilized base salt of naproxen. suprofen, .alpha.-methyl-(p-chlorobenzoyl)-5-methoxy-2-methylindole 3-acetic acid, flurbiprofen, carprofen, pranoprofen, benoxaprofen, alminoprofen, tiaprofenic acid, pirprofen, zaltoprofen, bermoprofen, loxoprofen, indoprofen, fenclorac, oxaprozin, fenbufen, orpanoxin, ketorolac, or clidanac, or a related compound thereof, is reacted with a compound of the general formula (6) wherein R2 represents H, alkyl, alkyloxy, alkenyl, or alkynyl residues having 1 to 12 carbon atoms, or aryl residues; R3 represents H, alkyl, alkyloxy, alkenyl, or alkynyl residues having 1 to 12 carbon atoms, or aryl residues; R4 represents H; Z represents halogen, or p-toluenesulphonyl, A- represents a negative ion; and n is 0, 1, 2, 3, 4, 5, 6, 7, 8, 9 or 10.

9. The process according to claim 8, wherein A- represents Cl-, Br-, F-, I-, AcO- or citrate.

10. A pharmaceutical composition comprising the compound of general formula (1) as defined in claim 1 or of the general formula 2 as defined in claim 2, and a pharmaceutically acceptable auxiliary or excipient.

11. The composition of claim 10, which is adapted for oral administration.

12. The composition of claim 10, which is adapted for transdermal administration.

13. The composition of claim 10, 11 or 12, which is for use in the treatment of a NSAIA-treatable condition in a human or animal.

14. The composition of claim 10, 11 or 12, which is for use in the treatment of pain from a toothache, headache, arthritis or other inflammatory pain, fever, cancer, dysmenorrhea, radiation-induced vomiting, diabetic neuropathy, acute migraine headache, hemophilic arthropathy, bone loss, or sunburn.

15. The composition according to claim 12, which is in the form of a solution, spray, lotion, ointment, emulsion or gel.

16. The composition according to claim 15, which is for the delivery of the compound of general formula (1) or of general formula (2) to a human or animal.

17. The composition of claim 10, which is for use in the topical treatment of pain selected from a headache, toothache, and muscle pain, and arthritis.

18. The composition of claim 10, which is for use in the topical treatment of inflammatory pain.

19. The composition according to claim 15, which is for use in the treatment of psoriasis, acne, or sunburn.

20. The composition of claim 10, for use in the treatment of asthma, the composition being in a form suitable for administration by spraying through the mouth or nose or other parts of a human or animal body.

21. The composition of claim 10, which is for use in the treatment of an eye inflammatory disease, ocular pain after corneal surgery, glaucoma, or ear inflammatory and/or painful condition in a human or animal.

22. The composition of claim 21, which is for use in the treatment of otitis in a human or animal.

23. Use of the compound as defined in any one of claims 1 to 3, in the preparation of a medicament for the treatment of a NSAIA-treatable condition in a human or animal.

24. Use of the compound as defined in any one of claims 1 to 3, in the preparation of a medicament for the treatment of pain from a toothache, headache, arthritis, fever, cancer, dysmenorrhea, radiation-induced vomiting, diabetic neuropathy, acute migraine headache, hemophilic arthropathy, bone loss, or sunburn.

25. Use of the compound as defined in any one of claims 1 to 3, in the preparation of a medicament for the treatment of inflammatory pain.

26. Use of the compound as defined in any one of claims 1 to 3, in the preparation of a medicament for the topical treatment of pain selected from headache, toothache, and muscle pain, and arthritis.

27. Use of the compound as defined in any one of claims 1 to 3, in the preparation of a medicament for the topical treatment of inflammatory pain.

28. Use of the compound as defined in any one of claims 1 to 3, in the preparation of a medicament for the transdermal treatment of psoriasis, acne, or sunburn.

29. Use of the compound as defined in any one of claims 1 to 3, in the preparation of a medicament for the treatment of asthma.

30. Use of the compound as defined in any one of claims 1 to 3, in the preparation of a medicament for the treatment of an eye inflammatory disease, ocular pain after corneal surgery, glaucoma, or ear inflammatory and/or painful condition in a human or animal.

31. Use of the compound as defined in any one of claims 1 to 3, in the treatment of a NSAIA-treatable condition in a human or animal.

32. Use of the compound as defined in any one of claims 1 to 3, in the treatment of pain from a toothache, headache, arthritis, fever, cancer, dysmenorrhea, radiation-induced vomiting, diabetic neuropathy, acute migraine headache, hemophilic arthropathy, bone loss, or sunburn.

33. Use of the compound as defined in any one of claims 1 to 3, in the treatment of inflammatory pain.

34. Use of the compound as defined in any one of claims 1 to 3, in the topical treatment of pain selected from headache, toothache, and muscle pain, and arthritis.

35. Use of the compound as defined in any one of claims I to 3, in the topical treatment of inflammatory pain.

36. Use of the compound as defined in any one of claims 1 to 3, in the transdermal treatment of psoriasis, acne, or sunburn.

37. Use of the compound as defined in any one of claims 1 to 3, in the treatment of asthma.

38. Use of the compound as defined in any one of claims 1 to 3, in the treatment of an eye inflammatory disease, ocular pain after corneal surgery, glaucoma, or ear inflammatory and/or painful condition in a human or animal.

39. A transdermal therapeutic application system, for the treatment of an NSAIA-treatable condition in a human or animal, comprising a matrix layer comprising as the active ingredient the compound as defined in any one of claims 1 to 3; and an impermeable backing layer.

40. The application system according to claim 39, which is a bandage or a patch.

41. The application system according to claim 39 or 40, wherein the active ingredient is in a reservoir which has a permeable bottom facing away from the impermeable backing layer.

42. A compound that is diethylaminoethyl .alpha.-methyl-4-(2-thienylcarbonyl)benzeneacetate.HA, wherein A represents a negative ion.

43. A compound that is diethylaminoethyl .alpha.-methyl-(p-chlorobenzoyl)-5-methoxy-2-methylindole 3-acetate.HA, wherein A represents a negative ion.

44. A compound that is diethylaminoethyl 2-(2-fluoro-4-biphenylyl)propionate.IIA, wherein A represents a negative ion.

45. A compound that is diethylaminoethyl 6-chloro-.alpha.-methyl-9H-carbazole-2-acetate.HA, wherein A represents a negative ion.

46. A compound that is diethylaminoethyl .alpha.-methyl-5H-[1]
benzopyrano[2,3-b]pyridine-7-acetate.HA, wherein A represents a negative ion.

47. A compound that is diethylaminoethyl 2-(4-chlorophenyl)-.alpha.-methyl-benzoxazoleacetate.HA, wherein A represents a negative ion.

48. A compound that is diethylaminoethyl .alpha.-methyl-4-[(2-methyl-2-propenyl)amino]benzeneacetate.HA. wherein A represents a negative ion.

49. A compound that is diethylaminoethyl 5-benzoyl-.alpha.-methyl-2-thiopheneacetate.HA, wherein A represents a negative ion.

50. A compound that is diethylaminoethyl 3-chloro-4-(2,5-dihydro-1H-pyrrol-yl)-.alpha.-methyl benzeneacetate.HA, wherein A represents a negative ion.

51. A compound that is diethylaminoethyl 2-(10,11-dihydro-10-oxodibenzo(b,f)thiepin-2-yl)propionate.HA, wherein A represents a negative ion.

52. A compound that is diethylaminoethyl 2-(8-methyl-10,11-dihydro-11-oxodibenz(b,f)oxepin-2-yl)propionate.HA, wherein A represents a negative ion.

53. A compound that is diethylaminoethyl 2-[4-(2-oxocyclopentyl-methyl)phenyl]propionate.HA, wherein A represents a negative ion.

54. A compound that is diethylaminoethyl 4-(1,3-dihydro-1-oxo-2H-isoindol-2-yl)-.alpha.-methylbenzeneacetate.HA, wherein A represents a negative ion.

55. A compound that is diethylaminoethyl .alpha.,3-dichloro-4-cyclohexylbenzeneacetate.HA, wherein A represents a negative ion.

56. A compound that is diethylaminoethyl 4,5-Diphenyl-2-oxazole propionate.HA, wherein A represents a negative ion.

57. A compound that is diethylaminoethyl 3-(4-biphenylylcarbonyl)propionate.HA, wherein A represents a negative ion.

58. A compound that is diethylaminoethyl 5-(4-chlorophenyl)-beta-hydroxy-2-furanpropionate.HA, wherein A represents a negative ion.

59. A compound that is diethylaminoethyl 5-benzoyl-2,3-dihydro-1H-pyrrolizine-1-carboxylate.HA, wherein A represents a negative ion.

60. A compound that is diethylaminoethyl 6-chloro-5-cyclohexyl-2,3-dihydro-indene-1-carboxylate.HA, wherein A represents a negative ion.

61. A compound that is S-diethylaminoethyl 2-(2-fluoro-4-biphenylyl)propionate.HA, wherein A represents a negative ion.

62. A compound that is N-diethylaminoethyl 5-benzoyl-2,3-dihydro-1H-pyrrolizine-1-carboxylamide.HA, wherein A represents a negative ion.

63. A compound that is N-diethylaminoethyl 4,5-Diphenyl-2-oxazole propionamide.HA, wherein A represents a negative ion.