Description of the Prior Art Various compounds such as AZT (3'-azido-3'-deoxythymi- dine), DDC (2', 3'-dideoxycytidine), DDI (2', 3'-dideoxyino- sine), D4T (3'-deoxy-2', 3'-didehydrothymidine) 3TC (lamivudine), Ziagen, Nevirapine, Sustiva, Delavirdine, Indinavir, Ritonavir, Viracept, Saquinavir and Agenerase have been reported to have the ability, albeit limited, to inhibit the reproduction of AIDS virus. However, they are also known to cause undesirable side effects due to their toxicity as well as to induce the mutation of the virus, thereby increasing the resistance of the virus.

In order to minimize such problems, therefore, many attempts have been made. For example, there have been reported 2,4-pyrimidinedione derivatives having 1- alkoxymethyl substituents {J. Med. Chem., 35,4713 (1992); J. Med. Chem., 35,337 (1992); J. Med. Chem., 34,1508 (1991); J. Med. Chem., 34,1394 (1991); J. Med. Chem., 34, 349 (1991); Molecular Pharm., 39,805 (1991); Tet. Lett., 35,4531 (1994); J. Med. Chem., 38,2860 (1995); Nucleosides and Nucleotides, 14,575 (1995); J. Med. Chem., 39,2427 (1996); J. Med. Chem., 42,4500 (1999); EP 0,449,726 A1; EP 0,420,763 A2; USP 5,278,167; USP 5,318,972; USP 5,461,060 ; W095/18109 A1; and USP 1-allyl or propargyl substituents (USP 5,747,500); and 1-cyclopentenylmethylene

substituents (USP 5,922,727). Although these compounds exhibit improved activity against human immunodeficiency virus (HIV), there exists a need to develope non-toxic compounds having even higher potency against both wild-type and mutant HIV.

Summary of the Invention Accordingly, it is a primary object of the present invention to provide a novel compound having superior antiviral activity against both wild-type and mutant HIV-1 as well as reduced toxicity.

It is another object of the present invention to provide a pharmaceutical composition containing same.

It is a further object of the present invention to provide a process for the preparation of said novel compound.

In accordance with one aspect of the present invention, there is provided a novel 2,4-pyrimidinedione compound of formula (I) or a pharmaceutically acceptable salt thereof: wherein: R1 is a C., Q aryl or C3-10 heteroaryl group optionally having one or more substituents selected from the group consisting of halogen, C16 alkyl, C16 alkyl substituted with one or more halogen atoms, C36 cycloalkyl, cyano, nitro, hydroxy, thiohydroxy, azido, C16 alkoxy, oximino, C13 alkyloximino, O- (C16 alkyl)-substituted oximino,C alkylcarbonyl, C36 cycloalkylcarbonyl, hydroxymethyl, azidomethyl, C16 alkoxymethyl, C16

carbamoyloxymethyl, aminomethyl, N-(C13 alkyl) aminomethyl, N, N-di (C13 alkyl) aminomethyl, carboxy, Cl-6 alkoxycarbonyl, aziridine, amino,. hydroxyethylamino, cyclopropylamino, Cl-6 alkylamino, di (C16 alkyl) amino, trifluoroacetamido, Cl-6 acylamido, carbamoyl, hydroxyethylcarbamoyl, cyclopropylcarbamoyl, C16 alkylcarbamoyl, di (CI-6 alkyl) carbamoyl, aminocarbamoyl, dimethylaminocarbamoyl, hydrazino, 1,1-dimethylhydrazino, imidazolyl, triazolyl and tetrazolyl; a tetrahydropyridyl or piperidyl group optionally substituted with a C16 alkyl or C16 alkoxycarbonyl group; a tetrahydropyranyl group; or a tetrahydrofuryl group; R2 is hydrogen, halogen, nitro, cyano, C13 alkoxycarbonyl, C13 alkylamino, di (C13 alkyl) amino, Cl3 alkylcarbamoyl, di (Cl-3 alkyl) carbamoyl, C16 alkyl, C36 cycloalkyl or benzyl; R3 and R4 are each independently hydrogen, halogen, hydroxy, cyano, nitro, amino, acetamido, trifluoroacetamido, azido, C13 alkyl, C13 alkyl substituted with one or more halogen atoms, C13 alkoxycarbonyl, carbamoyl, C13 alkylcarbamoyl, di (C13 alkyl) carbamoyl or C13 alkoxy; A is 0 or S; and Z is 0, S, C=O, NH or CH2.

Detailed Description of the Invention Among the compounds of formula (I) of the present invention, the preferred are those wherein R1 is a phenyl, pyridyl or N-oxopyridyl group optionally having one or more substituents as listed in formula (I).

The 2,4-pyrimidinedione compound of formula (I) may be prepared by coupling a compound of formula (II) with a compound of formula (III), as shown in the Reaction Scheme A: Reaction Scheme A

wherein: R1, R2, R3, R4, A and Z have the same meanings as defined in formula (I) above; Z'is same as Z with the proviso that when A is oxygen, it can be a acetamido group; and Y is a suitable leaving group, e. g., halogen, methanesulfonyl, toluenesulfonyl or trifluoromethane- sulfonyl.

In Reaction Scheme A, the above reaction may be conducted in a solvent in the presence of a base at a temperature ranging from-10 to 100°C, wherein the molar ratio of the compound of formula (II) to the compound of formula (III) may range from 1: 0.8 to 1: 1.2. Representative examples of the base include lithium hydride, sodium hydride, potassium hydride, sodium carbonate, potassium carbonate and the like. Suitable for use in this reaction is a polar solvent such as acetonitrile, hexamethylphosphoramide (HMPA), dimethylsulfoxide (DMSO) and dimethylformamide (DMF).

The compounds of formula (II) may in some cases be prepared in accordance with the procedure disclosed in USP 5,747,500. Alternatively, the compounds of formula (II) may be advantageously prepared in some special cases by the procedure illustrated in Reaction Scheme B: Reaction Scheme B Method (i): Useful when A is 0 and Z'is acetamido Method (ii): Useful when A is O, Z'is C=O and R3 (or R4) is NO2 wherein, R2, R3 and R4 have the same meanings as defined in formula (I).

In accordance with the method (i) in Reaction Scheme B, a compound of formula (IV) which may be prepared by way of a known method disclosed in, e. g., Ber., 52B, 869 (1919) and J. Med. Chem., 7,808 (1964), is subjected to a coupling reaction with an arylformamide derivative in a polar solvent, e. g., dimethylformamide, in the presence of a strong base, e. g., sodium hydride, under a nitrogen atmosphere to provide a compound of formula (V) (Step (a)).

The compound of formula (V) is reacted with sodium methoxide in methanol to give a compound of formula (VI) (Step (b)).

Then, the compound of formula (VI) is demethylated and acetylated by the action of acetylbromide to provide a compound of formula (II-a) (Step (c)).

In the method (ii) of Reaction Scheme B, the compound of formula (IV) is reacted with a arylacetonitrile derivative in a polar solvent, e. g., dimethylformamide, in the presence of a base, e. g., sodium hydride, to provide a compound of formula (VII) (Step (d)), which is reacted with sodium methoxide in methanol to give a compound of formula (VIII) (Step (e)). Thereafter, the compound of formula (VIII) is reacted with a base, e. g., sodium hydride, in a polar solvent, e. g., dimethylformamide, in the presence of oxygen to provide a compound of formula (IX) (Step (f)), which is hydrolyzed with an acid, e. g., hydrochloric acid, to provide a compound of formula (II-b) (Step (g)).

Each of the compounds of formula (II-a) and (II-b) may be converted to one of the compounds of formula (II) containing various substituents via further reactions.

In this regard, in accordance with another aspect of the present invention, there is provided a compound of formula (II):

wherein: R'2 is ethyl or isopropyl; R'3 is nitro, amino, acetamido, trifluoroacetamido or alkoxycarbonyl; R'4 is methyl or halogen; and Z"is C=O, NH or acetamido.

Exemplary compounds of formula (I) of the present invention which can be prepared in accordance with the methods described above are listed in the following Table 1: Table 1 Comp. | A Z R1 R2 R3 | R4 ~Comp. A z R'R2 R3 R4 1 O C=O N Isopropyl CH3 CH3 I I2 O C=O > Isopropyl CH3 CH3 N :/ 3 C=O,-isopropyl CH3 CH3 \QN- 4 O C=O Ethyl CH CH3 5 O C=O Ethyl CH3 CH3 6 O C=O Ethyl CH CH N Isopropyl CH3 F I8 O C=O > Isopropyl CH3 F 9 O C=O > Isopropyl CH3 F Table 1 (Continued) : Comp. A Z R R2 10 O 1 C=O NS Ethyl CH3 F 11 0 C=O Ethyl CH 12 O C=O Ethyl CH3 F 13 O C=O N Isopropyl F F N lsopropyl F F 15 O C=O l Isopropyl F F N 16 O C=O N Ethyl F F 17 O C=O G Ethyl F F F F 18 O C=O N Ethyl F F Table 1 (Continued) Comp. A z Ri R2 R 3 R4 19 O C=O N Isopropyl Cl Cl l2 C=O N, Ethyl CI CI 21 O C=O N Isopropyl CH3 Cl 22 O C=O NS Isopropyl CH2F CH3 23 O C=O NS Ethyl CH2F CH3 24 O O N Isopropyl CH3 CH3 lEthyl CH3 CH3 26 O S ltm Isopropyl Cl Cl 27 Isopropyl CH3 CH3 Table 1 (Continued) Comp. A Z _ R2 R3 R4 28 O S NS Ethyl CH3 CH3 29 O C=O N Isopropyl CF3 CF3 30 p C=O N ./Ethyl CF3 CF3 31 p C=O N Isopropyl CF3 CF3 32 O C=O N Isopropyl CH3 H 33 Ethyl CH3 H 3 34 O C=O NS Isopropyl H H 35 O C=O N Ethyl H H 36 O C=O Isopropyl CH3 CH3 Table 1 (Continued) Comp. A z R R 3 R4 C=O Eth I -Y CH3 CH3 38 ozN I 1- 39 0 C=O H3CO m Isopropyl CH3 CH3 H3C 40 O C=O Isopropyl CH 41 0 C=O 02NS Ethyl C H3 C H3 42 o C=O H3COw Ethyl CH3 CH3 R F 43 o C=O FW Isopropyl CH3 C H3 F F 44 p C=p 44 0 C=O F3C Isopropyl CH3 CH3 F3C HIC 45 O C=0 _ Isopropyl CH3 CH3 Table 1 (Continued) Comp. A Z R R R R 46 O C=O H3CS Isopropyl CH3 F 'y" HC 47 0 C=O H3C Isopropyl C H3 Cl N- 48 O C=O H3CNS Isopropyl Cl Cl ' Lj r 49 O C=O H3CNS Isopropyl C H2F C H3 nez 50 O C=O H3C Isopropyl CH3 H 'W 0 51 O C=O CNS Isopropyl CH3 CH3 J HsC 52 O C=O NS Ethyl CH3 CH3 0 53 C=O H3 F 54 O C=O ci Ethyl CH3 CH3 N Table 1 (Continued) Coinp. A Z H3C 55 O C=O H3CN Isopropyl CH3 CH3 HgC H3C 56 56 a N,-Isopropyl F F HIC H3C 57 O C=O N Isopropyl Cl Cl HH33C S8 58 0 C=O HH33C HgC 59 O C=O Ny Isopl-opyl Cl CH3 H3C 60 0 C=O H3C Ethyl CH3 CH3 Hz HsC H3C 61 0 C=O Ethyl F F HgC NC 62 C=O nu 63 o C=O N, Isopropyl CH3 CI Table 1 (Continued) Comp. A Z R1 R2 R3 Ra 64 O C=O N3 Isopropyl C H3 No2 HgC 65 O C=O NS Isopropyl CH3 No2 Nez 66 NH NV Isopropyl CH3 CH3 67 0 NH N3 Ethyl C H3 CH3 Isopropyl CH3 CH3 69 O C=O H3 Isopropyl CH3 CH3 O-N Hic HIC 70 Isopi CH3 3 HIC H3C 71 0 C=0 o-N Isopropyl CH3 CI HIC HIC AcOH 2C 72 O C=O NS Isopropyl CH3 CH3 HoC 73 0 C=O H3C Iso propyl CH3 C H 3 r AcOH2C Table 1 (Continued) Comp. A z R R R R H3C 74 O C=0"L)-tsopropy) CH3 CI AcOHsC HOHC 75 0 C=O =\) Isoplopyl CH3 CH3 H3C HC 76 0 C=O N, Isopropyl CH3 CH3 HOHzC HsC- 77 O C=0 N Isopropyi CH3 CI HOHzC CHsOzC 78 0 C=0 NS Isopropyl CH3 CH3 NH NHZOC 79 0 C=0 NH2ocS Isopropyl CH3 CH3 N,) I- NU-, OC 80 0 C=O NH2ocS Isopropyl CHs C I 81 0 C=0 H2Nv Isopropyi CH3 CH3

Furthermore, the present invention encompasses, within its scope, pharmaceutically acceptable salts of the 2,4- pyrimidinedione compounds of formula (I). Suitable pharmaceutically acceptable salts of the compounds of formula (I) possessing strong antiviral activity against wild-type and mutant HIV-1 may include alkali or alkaline earth metal salts, e. g., sodium, potassium, magnesium and calcium salts thereof.

The present invention also includes within its scope pharmaceutical compositions comprising one or more of the compounds of formula (I) or their above-mentioned salts as the active ingredient, in association with pharmaceutically acceptable carriers, excipients or other additives, if necessary.

The pharmaceutical compositions of the invention may be formulated for administration orally or by injection. The composition for oral administration may take various forms such as tablets and gelatin capsules, which may contain conventional additives such as a diluent (e. g., lactose, dextrose, sucrose, mannitol, sorbitol, cellulose and glycine), a lubricant (e. g., silica, talc, stearic acid or its magnesium and calcium salts and polyethylene glycol).

In the case of the tablet form, the composition may further comprise a binder (e. g., magnesium aluminum silicate, starch paste, gelatin, tragacanth, methyl cellulose, sodium carboxymethyl cellulose and polyvinyl pyrrolidone) and optionally a disintegrant (e. g., starch, agar and alginic acid or its sodium salt), absorbent, colorant, flavor, sweetener and the like. The composition for injection may be an isotonic solution or a suspension.

The composition may be sterilized and/or contain an adjuvant such as a preservative, stabilizer, wetting agent, emulsifier, a salt for controlling an osmotic pressure and/or a buffer solution, and other pharmaceutically effective materials.

The pharmaceutical compositions can be prepared by a conventional mixing, granulating or coating method and may

contain preferably about 0.1 to 75 %, more preferably about 1 to 50 % of the active ingredient of this invention. The unit dosage of the composition suitable for administering a person weighing about 50 to 70 kg may contain about 10 to 200mg of the active ingredient.

The following Preparations and Examples are given for the purpose of illustration only and are not intended to limit the scope of the invention.

In the Preparations and Examples, unless otherwise specified, the evaporation was conducted under reduced pressure, preferably under a pressure ranging from about 15 to 100 mmHg.

Preparations The compounds of formula (II) having the structures (A) to (U), (II-a-1), (II-a-2) and (II-b-1) shown in Table 2 together with their melting points and NMR data were used in preparing respective compounds of formula (I) of the present invention.

Preparations 1 to 21 Each of the compounds having the specified structures (A) to (U) was prepared in accordance with the procedure described in USP 5,747,500.

Preparation 22 : Synthesis of 5-isopropyl-6- (3', 5'- dimethylphenylacetamido)-2, 4-pyrimidinedione (Compound (II- a-1)) Step 1) Synthesis of 2,4-dichloro-5-isopropyl-6- (3', 5'- dimethylphenylformylamido) pyrimidine To a magnetically stirred DMF solution (80ml) of 3,5- dimethylformaniline (8.94g, 60mmol) cooled in an ice bath, 60% sodium hydride dispersion (2.88g, 72mmol) was added portionwise under a nitrogen atmosphere. After 10min, 5- isopropyl-2,4,6-trichloropyrimidine (16.2g, 72mmol) was added thereto and the reaction mixture was allowed to warm

to room temperature, followed by stirring for 24hr. Ether was then added to the reaction mixture, and the organic layer was washed with water, dried over anhydrous magnesium sulfate, and filtered. The solvent was removed under reduced pressure and the resulting residue was purified by flash chromatography (eluent-ether: hexane=1: 15) to afford 3.3g (yield 17%) of the title compound as a white solid.

M. p. : 151 to 153 °C 1H-NMR (200MHz, CDC13) b 1.12-1.24 (6H, m), 2.30 (6H, s), 3.22 (1H, m), 6.72 (2H, s), 6.96 (1H, s), 8.70 (1H, s) m/z (EI) 338 (M+).

Step 2) Synthesis of 2,4-dimethoxy-5-isopropyl-6- (3', 5'- dimethylphenylamino) pyrimidine Sodium (1.02g, 44mmol) was added portionwise to a stirred anhydrous methanol (40ml) at room temperature under a nitrogen atmosphere to prepare sodium methoxide solution.

The compound obtained in Step 1) (3g, 8.88mmol) was added to the solution and the mixture was refluxed for 4hr. The reaction mixture was allowed to cool to room temperature and neutralized with excess ammonium chloride. The solvent was removed under reduced pressure and the resulting residue was purified by flash chromatography (eluent-ethyl acetate: hexane=1: 15) to afford 2.6g (yield 97%) of the title compound as a white solid.

M. p. : 126 to 127 °C lH-NMR (200MHz, CDC13) 6 1.31 (6H, d, J=7.1Hz), 2.31 (6H, s), 3.12 (1H, m), 3.92 (3H, s), 3.93 (3H, s), 6.44 (1H, s), 6.70 (1H, s), 7.21 (2H, s) m/z (EI) 301 (M+).

Step 3) Synthesis of 5-isopropyl-6- (3', 5'- dimethylphenylacetamido)-2,4-pyrimidinedione The compound obtained in Step 2) (2.6g, 8.6mmol) was refluxed with acetyl bromide (30ml) for 19hr. The reaction mixture was allowed to cool to room temperature and the solvent was removed under reduced pressure. The resulting

residue was purified by flash chromatography (eluent-ethyl acetate: hexane=2: 1) to afford 2.6g (yield 96%) of the title compound as a white solid.

Preparation 23 : Synthesis of 5-ethyl-6- (3', 5'- dimethylphenylacetamido)-2,4-pyrimidinedione (Compound (II- a-2)) The procedure of Preparation 22 was repeated using 5- ethyl-2,4,6-trichloropyrimidine in place of 5-isopropyl- 2,4,6-trichloropyrimidine to prepare the title compound.

Preparation 24 : Synthesis of 5-isopropyl-6- (3'-nitro-5'- methylbenzoyl)-2,4-pyrimidinedione (Compound (II-b-1)) <BR> <BR> <BR> <BR> <BR> <BR> <BR> <BR> Step 1) Synthesisof2, 4-dichloro-5-isopropyl-6-(a-cyano-3'- nitro-5'-methylbenzyl) pyrimidine To a magnetically stirred DMF solution (30ml) of 3- nitro-5-methylphenylacetonitrile (2.64g, 15mmol) and 5- isopropyl-2,4,6-trichloropyrimidine (4.05g, 18mmol) cooled in an ice bath, 60% sodium hydride dispersion (1.15g, 30mmol) was added portionwise under a nitrogen atmosphere.

After stirring for 2hr, the reaction mixture was allowed to warm to room temperature and stirred for 16hr. The reaction mixture was then neutralized with aqueous ammonium chloride and ethyl ether was added thereto. The organic layer was washed with water, dried over anhydrous magnesium sulfate, and filtered. The solvent was removed under reduced pressure and the resulting residue was purified by flash chromatography (eluent-ethyl acetate: hexane=1: 4) to afford 3.99g (yield 73%) of the title compound as a white solid.

M. p. : 124 to 125 °C 1H-NMR (200MHz, CDC13) 6 1.23 (3H, d, J=7.2Hz), 1.38 (3H, d, J=7.2Hz), 2.51 (3H, s), 3.34 (1H, m), 5.60 (1H, s), 7.57 (1H, s), 7.99 (1H, s), 8.07 (1H, s) m/z (EI) 365 (M+).

Step 2) Synthesis of 2,4-dimethoxy-5-isopropyl-6-(a-cyano- 3'-nitro-5'-methylbenzyl) pyrimidine To a stirred anhydrous methanol solution (60ml) of the compound obtained in Step 1) (3.65g, 10mmol), sodium methoxide (3.24g, 60mmol) was added at room temperature under a nitrogen atmosphere and refluxed for 24hr. The reaction mixture was then allowed to cool to room temperature and neutralized with excess ammonium chloride.

After removing the solvent, the resulting residue was purified by flash chromatography (eluent-ether: hexane=1: 3) to afford 1.8g (yield 50%) of the title compound as a light yellow solid.

M. p. : 134 to 135 °C 1H-NMR (200MHz, CDC13) 6 1.15 (3H, d, J=6.7Hz), 1.20 (3H, d, J=6.7Hz), 2.49 (3H, s), 3.05 (1H, m), 4.00 (3H, s), 4.01 (3H, s), 5.48 (1H, s), 7.62 (1H, s), 8.00 (2H, s) m/z (EI) 356 (M+).

Step 3) Synthesis of 2,4-dimethoxy-5-isopropyl-6- (3'-nitro- 5'-methylbenzoyl) pyrimidine To a stirred DMF solution (20ml) of the compound obtained in Step 2) (1.7g, 4.7mmol), 60% sodium hydride dispersion (283mg, 7. lmmol) was added at room temperature under a nitrogen atmosphere. The mixture was then stirred in the presence of oxygen. After 5hr, the reaction mixture was neutralized with ammonium chloride and ethyl ether was added thereto. The organic layer was washed with water, dried over anhydrous magnesium sulfate, and filtered. The solvent was removed under reduced pressure and the resulting residue was purified by flash chromatography (eluent- dichloromethane: hexane=97: 3) to afford 1.03g (yield 62%) of the title compound as a white solid.

M. p. : 111 to 112 °C 1H-NMR (200MHz, CDC13) 8 1.21 (6H, d, J=6.9Hz), 2.54 (3H, s), 2.88 (1H, m), 3.93 (3H, s), 4.09 (3H, s), 8.05 (1H, s), 8.27 (1H, s), 8.44 (1H, s) m/z (EI) 345 (M+).

Step 4) Synthesis of 5-isopropyl-6- (3'-nitro-5'- methylbenzoyl)-2,4-pyrimidinedione The compound obtained in Step 3) (630mg, l. 8mmol) was refluxed with conc. hydrochloric acid (6ml) for 4hr and the reaction mixture was allowed to cool to room temperature.

The precipitate was then collected, washed with distilled water and hexane, and dried to give 560mg (yield 98%) of the title compound as a white solid.

Table 2 rep Prep. Comp. Sti-ucture M. p. (tC) 1H-NMR No. 0 cH3 (200MHz, CDCl/CD30D) 8 : 1/A\ )! r!) OQQ-oqo 1. (A) HN 1 1 238-239 1. 16 (6H, d, J=6.9Hz), 2.35-2.49 (7H, m), H o 7.35 (2H, s). 7.53 (2H, s). o cH3 (200MHz, CDCIs/CD30D) 8 : 2 (B) TjjLl 249-250 0.97 (3H, t, J=7.4Hz), 2.17 (2H, q, o 0 J=7.4Hz), 2.39 (6H, s), 7.32 (1H, s), 7.50 (2H, s). ________________ o (200MHz, CD30D/DMSO-d6) d : 3 (C) HN 251-252 1.36 (6H, d, J=6.9Hz), 2.38 (1H, m), ° "3 2.46 (3H, (3H, s), 26 (1H, d, J=9. OHz), 7.43 (1H, d, J=8.4Hz), 7.52 (1H, s). (200MHz, CDsOD/DMSO-ds) : 0 F 4 (D) HN %) 235-236 0. 99 (3H, t, J=7. 4Hz), 2.17 (2H, q, CH3 J=7.4Hz), 2.50 (3H, s), 7.44 (1H, d, H o J=9.4Hz), 59 (1H, d, J=8.8Hz), 7.70 (1H, m). 0 gu F (200MHz, CDC13/CD30D) d : 5 (E) O 23 233-234 1. 06 (6H, d, J=7.0Hz), 2.32 (1H, m), H 7.07 (1H, m), 7.25-7.38 (2H, m). ______ o | I (200MHz, CDCl3/CD30D) A : 6 (F) °><lF 211-212 0. 88 (3H, t, J=7. 3Hz), 2.06 (2H, q, H o J=7.3Hz), 7.06 (1H, m), 7.32-7.37 (2H, m) ? | (200MHz, CD30D) 8 : 7 1.16 (6H, d, J=7.0Hz), 2.45 (1H, i-ii), H 7. 61-8.02 (5H, m) _____________ 0 ? | (200MHz, CD30D) d : 8 (H) HN 218-219 0.98 (3H, t, J=7. 5Hz), 2.17 (2H, q, ZON H o J=7.5Hz), 7.58-8. 03 (5H, m) _______ o cF3 (200MHz, CDCIs/CDsOD) 9 (I) HN 1 220-221 1.17 (6H, d, J=6.8Hz), 2.39 (l. li, o w, cF3 0 8. 21 (1H, s), 8.37 (2H, s).

Table 2 (Continued) - Prep. Structure M. p. ('C)'H-NMR No. o, > (200MHz, CDCI3/CD30D) a : 10 (J) 227-228 1.13 (6H, d, J=7.0Hz), 2.35-2.50 (4H, m), Oit 7. 42-7.72 (4H, m), 9.82 (1H, s). o (200MHz, CDC13/CD30D) 3 : 11 (K) N 236-237 0.97 (3H, t, J=7.5Hz), 2.18 (2H, q, H o J=7.5Hz), 2.44 (3H, s), 7.287. 71 (4H, m), 9.70 (lH, s). ________________ o I c (200MHz, CDCI3/CD30D) A : HN) 12 (L) HN I I cl 252-253 1. 11 (6H, d, J=6.9Hz), 2.33 (1H, m), H 7. 61-7.73 (3H, m). ________ ___ o cl (200MHz, CDCl3/CDsOD) d : ij ? 13 (M) 1 242-243 0.90 (3H, t, J=7.5Hz), 2.07 (2H, q, ° H o Cl J=7.5Hz), 7.59 (1H, t, J=1.8Hz), 7.67 (2H, d, J=1.8Hz). ________________ 3 s c (200MHz, CDCl3/CD30D) d : 14 (N) 0), N 254-255-2.45 (4H, m), O H CH3 ho?. 50-7. 71 (3H, m). O CH2F (200MHZ, CDCI3/CD30D) d : O CH 15 (0) 1 218-219 1.10 (6H, d, J=6.9Hz), 2.32-2.52 (4H, m), 0 T 5. 41 (2H, d, J=47. OHz), 7.51-7.70 (3H, m), 9.15 (1H, s), 9.66 (1H, s). _________ (200MHz, CDCIs/CDsOD) 0) CH2F 16 (P) 01 224-225 0.98 (3H, t, J=7.4Hz), 2.16 (2H, q, H o J=7. 4Hz), 2.47 (3H, s), 5.43 (2H, d, J=47. 2Hz), 7.54-7.71 (3H, m). _______ o L CH3 (200MHz, CDsOD) 17 D'i ! ft) 790-70 17 (Q) HN 229-230 l.'-) 0 (6H, d, J=7. lHz), 2.33 (6H, s), O H O CH3 3.35 (1H, m), 6.64 (2H, s), 6.83 (111, s). o eCH3 (200MHZ, CD30D) d : 10/p\ 'Trr!) 771-779 18 (R) 221-222 0. 90 (311, t, J=7. 4Hz), 2. 17-2. 25 (8H, m), O H O CH3 6.62 (2H, s), 6.78 (1H, s).

Table 2 (Continued) Prep. Comp. Sti-ucture M. p CO'H-NMR No. (200MHz, CDC13) 8 : o t CH3 19 (S) 225-226 1.34 (6H, d, J=7.0Hz), 2.35 (6H, s), O H S CH3 3. 11 (1H, m), 7.14 (1H, s), 7.16 (2H, s), 9.30 (1H, s). ________________ (200MHz, DMSO-ds) 8 : o i 3.22 (1H, m), 20 (T) 224-225 1.17 (6H, d, J=6.8Hz), 3. 22 (1H. m), o 7. 42 (2H, s), 7.56 (1H, s), 10.96 (1H, s), 11.18 (1H, s). _ (200MHz, CDCl3) d : o t CH3 21 (U) HN 224-225 1.14 (3H, t, J=7. 5Hz), 2.36 (6H, s), 2.55 (2H, H J=7. 5Hz), 7.06 (1H, s), (3H, m), 9.04 (1H, s) ______________ o cH3 (200MHz, CDCls) 8 : (II-a- 22 1) X 3 224-226 1.12-1.33 (6H, m), 2.02-2.15 (3H, m), CocHs 2. 31 (6H, s), 2.90 (1H, m), 6.99 (3H, s) o cH3 (200MHz, CDCl3) 8 : (II-a-HN 23 0. 93 (3H, t, J=7. 5Hz), 2.05-2.15 (3H, m), 2) o N cH3 , cocH3 2. 24-2.40 (8H, m), 6.94-6.99 (3H, m) __ 200MHz, CDC13/CI) 30D) d : 0 j NOs /TT1 li J__i 24 1.12 (6H, d, J=7.0Hz), 2.40 (1H, m), > CH3 2.54 (3H, s), 8.11 (1H, s), 8.37 (1H, s), 3. 49 (1H, s)

Example 1 : Synthesis of 1- (4'-picolyl)-5-isopropyl-6- (3', 5'-dimethylbenzoyl)-2,4-pyrimidinedione (Compound 1) To a magnetically stirred DMF solution (5ml) of compound (A) obtained in Preparation 1 (286mg, lmmol) maintained at room temperature, were added anhydrous potassium carbonate (276mg, 2mmol), lithium iodide (134mg, lmmol), and 4-picolyl chloride hydrochloride (164mg, lmmol), in this order. After stirring for 16hr, the solvent was removed under reduced pressure and the resulting residue was purified by flash chromatography (eluent-ethyl acetate: hexane=3: 1) to afford 120mg (yield 32%) of the title compound as a white solid.

M. p. : 264 to 265 °C 1H-NMR (200MHz, CDC13) 6 1.12 (3H, d, J=6.7Hz), 1.23 (3H, d, J=6.7Hz), 2.30-2.40 (7H, m), 4.66 (1H, d, J=16.3Hz), 4.88 (1H, d, J=16.3Hz), 6.98-7.36 (5H, m), 8.41-8.44 (2H, m), 9.91 (1H, s) m/z (EI) 377 (M+). <BR> <BR> <BR> <BR> <BR> <BR> <BR> <P>Example 2 : Synthesis of 1- (3'-picolyl)-5-isopropyl-6- (3', 5'-dimethylbenzoyl)-2,4-pyrimidinedione (Compound 2) The procedure of Example 1 was repeated using 3-picolyl chloride hydrochloride in place of 4-picolyl chloride hydrochloride to prepare the title compound.

M. p. : 179 to 180 °C 1H-NMR (200MHz, CDC13) 6 1.12 (3H, d, J=6.9Hz), 1.22 (3H, d, J=6.9Hz), 2.20-2.38 (7H, m), 4.71 (1H, d, J=16.0Hz), 4.93 (1H, d, J=16.0Hz), 7.09-7.56 (5H, m), 8.29-8.43 (2H, m), 10.18 (1H, s) m/z (EI) 377 (M+). <BR> <BR> <BR> <BR> <BR> <BR> <BR> <P>Example 3 : Synthesis of 1-(2'-picolyl)-5-isopropyl-6- (3', 5'-dimethylbenzoyl)-2,4-pyrimidinedione (Compound 3) The procedure of Example 1 was repeated using 2-picolyl

chloride hydrochloride in place of 4-picolyl chloride hydrochloride to prepare the title compound.

M. p. : 214 to 215 °C 1H-NMR (200MHz, CDC13) 6 1.12 (3H, d, J=6.9Hz), 1.23 (3H, d, J=6.9Hz), 2.20-2.40 (7H, m), 4.77 (1H, d, J=16.8Hz), 5.16 (1H, d, J=16.8Hz), (6H, m), 8.36 (2H, m), 9.90 (1H, s) m/z (EI) 377 (M+).

Examples 4 to 65 The procedure of Example 1 was repeated to obtain the 2,4-pyrimidinedione derivatives of Examples 4-65 shown in Table 3.

Table 3 Px Ex A Z R'R2 Rb R4'H-NMR (200MHz, CDCl3) 8 I\4. p. (°C) 0.97 (3H, t, J=7.3Hz), 2.05 (1H, m), 2.2 0-2.35 (7H, m). 4.70 (1H, d, J=16.4Hz), 4 O C=O M-Ethyl CHg CHg 4.90 (1H, d, J=16.4Hz), 6.98-7.01 (2H, 267-268 m), 7.27 (1H, s), 7.34 (2H, s), 8.41-8.4 4 (2H, m), 9.25 (1H, s). ____________ 0.95 (3H, t, J=7.3Hz), 2.02 (1H, s), 2.20-2.40 (7H, m), 4.72 (1H, d, 5 O C=O N/Ethyl CHs CH3 J=16.4Hz), 4.90 (1H, d, J=16.4Hz), 197-198 7.14 (lH, s), 7.34 (2H, s), 7.52 (1H, m), 8.29-8.43 (2H, m), 9.25 (1H, s). _____ 0.95 (3H, t, J=7.1Hz), 2.05 (1H, m), 2.20-2.40 (7H, m), 4.81 (1H, d, 6 O C=O > Etllyl CH3 CH3 J=16.4Hz), 5.14 (1H, d, J=16.4Hz), 235-236 7.01-7.52 (6H, m), 8.40 (1H, m), 9. 11 (1H,s). __________________ 1.14 (3H, d, J=6.7Hz), 1.23 (3H, d, J=6.7Hz), 2.22-2.38 (4H, m), 4.63 (1H, 7 O C=O Isopropyl CH3 F d, J=16.3Hz), 4.94 (1H, d, J=16.3Hz), 207-209 7.00-7. 36 (5H, m), 8.41-8.45 (2H, m). 9.56 (1H, s). __________________ 1.12 (3H, d, J=6.7Hz), 1.22 (3H, d, J=6.7Hz), 2.27 (1H, m), 2.34 (3H, s), 8 O Isopropyl CH3 F 4.64 (1H, d, J=15.6Hz), 5.00 (1H, d, 211-212 J=16.4Hz), 7.10-7.53 (5H, m), 8.27-8.42 (2H, m), 9.41 (iti. s). __ 1.13 (3H, d, J=6.9Hz), 1.22 (3H, d, J=6.9Hz), 2.20-2.35 (4H, m), 4.69 (1H, 9 O C=O Isopropyl CH3 F d, J=16.4Hz), 5.29 (1H, d, J=16.4Hz), 187-189 N 7.00-7.52 (6H, m), 8.37 (1H, m), 9.15 (1H, s). __________________ 0.98 (3H, t, J=7.3Hz), 2.05 (1H, m), 2.2 10 O C=O N Ethyl CH3 F 0-237 (7H, m), 4.70 (1H, d, J=16. 4Hz), 4. 92 (1H, d, J=16. 4Hz), 7.00-7.37(su, m), (2H, m), 10.39 (1H, s). ____ 0.95 (3H, t, J=7.3Hz), 2.02 (1H, m), 11 05 (lH, m), 2.33 (3H, s), 4.72 (1H, d, 189-l90 J=1G. 4Hz), 5. 02 (1H, d, J=1G. 4Hz), l11-7. 5G (5H, m), 8. 30-8. 49 (2H, m).7. 0.96 (3H, t, J=7. 3Hz), 2. 03 (1H, m). 12 =0 Ethyl CH3 F J=16. 4Hz), 5.23 (1H, d, J=16.4Hz), 158-159 J=1G. 4Hz), IJc. -IJ9 7.02-7.53 (6H, m), 8.39 (1H, m), 9.l ? (1H, s).- Table 3 (Continued) Ex. A Z R'R2 R3 R4 lH-NMR (200MHz, CDCl3) 8 Ad. p. (C) 1.15 (3H, d, J=7. OHz), 1.23 (3H, d, J=7. 0Hz), 2.26 (1H, m), 4.63 (1H, d, 13 0 C=O NS Isopropyl F F J=16.2Hz), 4.94 (1H, d, J=16.2Hz), 1. 89-190 6.97-7.26 (5H, m), 8.43-8.46 (2H, m), 8.90 (1H, s). _ 1.12 (3H, d, J=6.7Hz), 1.21 (3H, d, J=6.7Hz), 2.23 (1H, m), 4.630H, d, 14 O C=O N/Isopropyl F F J=15.8Hz), 5.06 (1H, d, J=15.8Hz), 227-230 7.01-7.54 (5H, m), 8.26 (1H, m), 8.42 (1H, m), 9.49 (1H, s). ___________ 1.15 (3H, d, J=6.9Hz), 1.22 (3H, d, J=6.9Hz), 2.23 (1H, m), 4.62 (1H, d, 15 O C=O e Isopropyl F F J=16.6Hz), 5.31 (1H, d, J=16.6Hz), 214-215 6.95-7.54 (6H, m), 8.37 (1H, m), 9.10 (1H, s). __________________ 0.97 (3H, t, J=7.4Hz), 2.02 (1H, m), 2 5 (lH, F , 4. 65-4.65-4. (2H, m), 16 O C=O N . gg_. 40 (5H, m), 8.43-8.46 (2H, m), 223-224 9.73 (1H, s). 0. 96 (3H, t, J=7.3Hz), 2.00 (1H, m), 2. 22 (1H, m), 4. 68 (1H, m), 5.04 (1H, 17 O C=O N Ethyl F F m), 7.03-7.27 (4H, m), 7.54 (1H, m), 217-218 8.28-8.44 (2H, m), 9.89 (1H, s). ____ 0.97 (3H, t, J=7.5Hz), 2.01 (1H, m), 18 0 C=O \ N m), 6. 95-7. 55 (GH, m), 8. 37 (1H, m), 9.03 (1H, s). _________________ 1.12 (3H, d, J=6.9Hz), 1.25 (3H, d, J=6.9Hz), 2.21 (1H, m), 4.59 (1H, d, 19 C=O N Isopropyl Cl Cl J=16.6Hz), 4.99 (1H, d, J=16.6Hz), 232-233 6.98 (2H, d, J=5.9Hz), 7.55 (3H, s), 8.44 (2H, d, J=5.9Hz). 0.98 (3H, t, J=7.5Hz), 2.05 (1H, m), 2.28 (1H, m), 4.68 (1H, d, J=16.5Hz), 20 O C=O N Ethyl Cl Cl 5.02 (1H, d, J=16.5Hz), ô. 98 (2H, d, 243-245 J=5.9Hz), 7.54-7.74 (3H, m), 8.45 (2H, d, J=5.9Hz), 9.36 (1H, s). __________ Table 3 (Continued) Ex A Z Rl R2 R3 R4 1H-NMR (200MHz, CDCl3) 8 M. p. ('C) 1. 14 (3H, d, J=ô. 7Hz), 1. 23 (3H, d, 1. 14 (3H, d, J=6. 7Hz), 1. 23 (3H, d, d, J=16. 3Hz), 4. 9 (li, d, J=16. 3Hz), '- d, J=16.3Hz), 4.95 (1H, d, J=16.3Hz), _6.97-8.44 (7H, m), 9.35 (1H, s). ____ 1.07 (3H, d, J=6.7Hz), 1.18 (3H, d, J=6.7Hz), 2.25 (1H, m), 2.32 (3H, s), 190 4. 61 (lu, d, J=16.4Hz), 4.84 (in, d, 22 O C=O N Isopropyl CH2F CH3 J=16. 4Hz), 5.29 (2H, d, J=47.2Hz), 6.97 (2H, d, J=5.9Hz), 7.39-7.53 (3H, m), 8.32 (2H, d, J=5.9Hz). __________ 0.97 (3H, t, J=7.5Hz), 2.04 (1H, m), 2.25 (1H, m), 2.36 (3H, s), 4.68 (1H, d, J=15. OHz), 4.94 (1H, d, J=15. OHz), 2333 (2H, d, J=47. 2Hz), G. 98-7. 01 (2H, m), 7.48 (1H, s). m), 9.48 (lu, s). _______________ 1.14 (6H, d, J=7.1Hz), 2.27 (6H, s), 2.84 (1H, m), 4.88 (2H, s), 6.44 (2H, s), Isopropyl CH3 CH3 6.75 (1H, s), 7.11 (2H, dd, J=4.5Hz, 213-215 J=1.6Hz), 8.54 (2H, dd, J=4.5Hz, J=1.6Hz), 9.79 (1H, s). ____________ 0.94 (3H, t, J=7.5Hz), 2.21 (2H, q, J=7.5Hz), 2.27 (6H, s), 4.92 (2H, s), 25 O O N-Ethyl CHs CHs 6.45 (2H, s), 6.76 (1H, s), 7.13 (2H, d, 229-230 J=6.1Hz), 8.54 (2H, d, J=6.1Hz), 8.95 (1H, s). ______________ ____ 1.21 (6H, d, J=6.9Hz), 3.33 (1H, m), 26 O S N Isopropyl Cl Cl 5.20 (2H, s), 6.81-7.11 (5H, m), 198-199 8.43-8.46 (2H, m), 9.70 (1H, s). ____ 1.26 (6H, d, J=6.9Hz), 2.21 (6H, s), 27 O S N (2H, s), 6. G5 (2H, s), 1gG-187 27 0 S Nv\ Isopropyl CH3 CH3 8.50 (2H, d, J=5.7Hz), 10.82 (1H, s). ____ 1.07 (3H, t, J=7.5Hz), 2.23 (6H, s), 2.73 (2H, q, J=7.5Hz), 5.21 (2H, s), 28 O S -Ethyl CHs CHs 6. 68 (2H, s), 6.82 (1H, s), 6.98 (2H, d, 191-192 J=6.3Hz), 8.48 (2H, d, J=6.3Hz), 8.97 (1H, s). _________________ Table 3 (Continued) Ex A Z Rl R2 R3 R4 lH-NMR (200A {Hz, CDCl3) 8 M. p. (°C) 1.14 (3H, d, J=6. 9Hz), 1.24 (3H, d, J=6.9Hz), 2.18 (1H, m), 4.51 (1H, d, 29 O C=O N J=16.3Hz), 5.28 (1H, d, J=16.3Hz), 236-237 6.95 (2H, d, J=6.1Hz), 8.07 (1H, s), 8.11 (2H, s), 8.37 (2H, d, J=6. lHz). 0.97 (3H, t, J=7.3Hz), 2.00-2.35 (2H, m), 4. 60 (1H, m), 5.22 (1H, m), 208-209 30 O C=O N Etllyl CF3 CF3 6. 94-6 98 (2H, m), 8.07 (3H, s), 208-209 _ _ 8.35-8.38 (2H, m), 9.73 (1H, s). ____ 1.14 (3H, t, J=6.7Hz), 1.23 (3H, d, J=6.7Hz), 2.16 (1H, m), 4.51 (1H, d, 31 O C=O > Isopropyl CF3 CF3 J=16.4Hz), 5.51 (1H, d, J=16.4Hz), 185-186 6.94-7.49 (3H, m), 8.03-8.32 (4H, m), 9. 61 (1H,s). __________________ 1.12 (3H, d, J=6.7Hz), 1.22 (3H, d, J=6.7Hz), 2.26-2.36 (4H, m), 4.65 (1H, 32 O C=O M-Isopropyi CHg H d, J=16.0Hz), 4.86 (1H, d, J=16.0Hz), 226-227 6.97 (2H, d, J=5.9Hz), 7.25-7.60 (4H, m), 838 (2H, d, J=5.9Hz). __________ 0.97 (3H, t, J=7.4Hz), 2.06 (1H, m), 2.26 (1H, m), 2.34 (3H, s), 4.72 (1H, d, 33 O C Ethyl CH3 H J=16.0Hz), 4.84 (1H, d, J=16.0Hz), 218-219 6.99-7.02 (2H, m), 7.29-7.62 (4H, m), 8.41-8.44 (2H, m), 9.93 (1H, s). ____ 1.15 (3H, d, J=6.9Hz), 1.25 (3H, d, J=6. 9Hz), 2.34 (1H, m), 4.70 (1H, d, 34 O C Isopropyl H H J=16.4Hz), 4.87 (1H, d, J=16.4Hz), 238-239 6.99-7.82 (7H, m), (2H, m), 10.16 (1H, s). _________________ 0.97 (3H, t, J=7.4Hz), 2.05 (1H, m), 35 0 C-0')-Ethvl H H -'-65-94 (2H, m) 35 24 (IH, m), 4.65-4.94 (2H, m) 219-220 6. 99-7.80 (7H, m), 8.40-8.44 (2H, m), 9 68 (lI-i, s). _________________ 1.08 (3H, d, J=6.9Hz), 1.21 (3H, d, J=6.9Hz), 2.20-2.40 (7H, m), 4.59 (lu, 36 0 C=O d, J=15.6Hz), 5.07 (1H, d, J=15.6Hz), 199-200 7.02-7.12 (5H, m), 7.18 (1H, s), 7.26 (2H, s), 8.85 (1H, s). ___________ Table 3 (Continued) Px . Ex. A Z R'R2 R3 Rq'H-NMR (2001IHz, CDCI3) 8 II. p. ( C) 0. 93 (3H, t, J=7.3Hz), 2.02 (1H, m), 2. 12-2. 28 (7H, m), 4.64 (1H, d, 37 O C=O Ethyl CHs CHs J-15_6Hz), 5.07 (1H, d, J=15.6Hz), 221-222 7.02-7.26 (8H, m), 8.97 (1H, s). ____ 1.12 (3H, d, J=6.9Ha), 1.22 (3H, d, J=6.9Hz), 2.20-2.40 (7H, m), 4.77 (1H, 38 0 C=O 02Nv Isopropyl CH3 CH3 d, J=16.0Hz), 4.98 (1H, d, J=16. OHz), 203-204 7.23-7.32 (5H, m), 8.00 (2H, d, J=8.5Hz), 8.97 (1H, s). _ 1.07 (3H, d, J=6.9Hz), 1.20 (3H, d, J=6.9Hz), 2.20-2.40 (7H, m), 3.69 (3H, 39 O C=O H3COo Isopropyl CH3 CH3 s), 4.50 (1H, d, J=15.2Hz), 5.07 (1H, d, 156-157 J=15.2Hz), 6.57-7.31 (7H, m), 8.74 (1H, s). __________________ 1.10 (3H, d, J=6.7Hz), 1.21 (3H, d, H3C J=6.7Hz), 2.11 (3H, s), 2.25-2.38 (7H, m), 4.34 (1H, d, J=15.8Hz), 5.23 (1 3, 40 O C=O v i Isopropyl CHs CHs d J-15. 8Hz), 6. GG (1H, s), 6. 77 (1H, 22G-227 ci s), 6.83 (1H, s), 7.19 (1H, s), 7.27 (2H, s), 8.72 (1H, s). ________________ 0.96 (3H, t, J=7.5Hz), 2.08 (1H, m), 2.20-2.40 (7H, m), 4.84 (1H, d, 41 O C=O o--Ethyl CHg CHs J=16. 6Hz), 5.00 (1H"d, J=16. 6Hz), 230-231 7.25-7.32 (5H, m), (2H, m), 9.43 (1H, s). _________________ 0.92 (3H, t, J=7.3Hz), 2.05 (1H, m), 2.10-2.40 (7H, m), 3.69 (3H, s), 42 O C=O HscoQ Ethyl CHg CHg 4.56 (1H, d, J=15.4Hz), 5.07 (1H, d, 157-158 J=15.4Hz), 6.59-7.26 (7H, m), 9.25 (1H, s). _________________ 1.12 (3H, d, J=6.9Hz), 1.22 (3H, d, F J=6.9Hz), 2.22-2.40 (7H, m), 4.54 (1H, 43 O C=O Isopropyl CH3 CH3d, J=16.3Hz), 4.99 (1H, d, J=16.3Hz), 208-209 F 6.50-6.60 (3H, m), 7.24 (1H, s), 7.35 (2H, s), 9.25 (1H, s). ___________ 1.12 (3H, d, J=6.9Hz), 1.23 (3H, d, F3C J=6.9Hz), 2.25 (6H, s), 2.30 (1H, m), 44 0 C=O 4.62 (1H, d, J=15.9Hz), 5.33 (1H, d, 184-185 J=15. 9Hz), (3H, m), 7. 51 (2H, s), 7.58 (1H, s), 9.92 (1H, s).

Table 3 (Continued) Ex Z R'R R R''H-NMR (200MHz, CDCIs) 1.05 (3H, d, J=6.7Hz), 1.15 (3H, d, H3C J=6.7Hz), 2.22-2. 32 (10H, m), 4.44 (1H, 45 O C=O Isopropyl CH3 CH3d, J=16.0Hz), 4.90 (1H, d, J=16.0Hz), 269-270 (2H, m), 7.16 (1H, s), 7.19 (2H, s), 8.20 (1H d,. T=5.5Hz), 8.82 (1H s). ____ 1.15 (3H, d, J=7.0Hz), 1.20 (3H, d, H3C J=7. 0Hz), 2.21 (1H, m), 2.24 (3H, s), 46-0 C=O Isopropyl CH3 F 2.34 (3H, s), 4.42 (1H, d, J=16.2Hz), 217-218 4.96 (1H, d, J=16.2Hz), 6.70-7.26 (5H, m), 8.21 (1H, d, J=5.9Hz), 9.25 (1H, s). ____ 1.14 (3H, d, J=6.7Hz), 1.22 (3H, d, H3C J=6. 7Hz), 2.22-2.38 (4H, m), 2.41 (3H, 47 O C=O Isopropyl CH3 Cl s), 4.46 (1H, d, J=16.2Hz), 5.07 (1H, d, 253-254 J=16.2Hz), 6.77-8.30 (6H, m), 9.50 (1H, s), 1.15 (3H, d, J=6.9Hz), 1.23 (3H, d, H3C J=6.9Hz), 2.23 (1H, m), 2.44 (3H, s), 48 O C=O Isopropyl Cl Cl 4.41 (1H, d, J=16.2Hz), 5.18 (1H, d, 234-236 J=16.2Hz), 6.75-8.30 (6H, m), 9.42 (1H, s). 1.12 (3H, d, J=6.7Hz), 1.22 (3H, d, J=6.7Hz), 2.26-2.37 (7H, m), 4.48 (1H, d, J=1G. 5Hz), 5. 5. 04 (1H, d, J=16.5Hz), 253-255 49 O C=0 N Isopropyl CHZF CHa 5. 31 (2H, d, J=47. 2H2), 6. 75-6. 78 (2H, m), 7.39-7.52 (3H, m), 8.24 (1H, m), 8.85 (lu, s). ___________________ 1.13 (3H, d, J=7.0Hz), 1.23 (3H, d, J=7. OHz), 2.24-2.39 (7H, m), 4.54 (1H, d, 50 O C=O N,-D/J=16. lHz), 4. 95 (IH,, d, J=16. lHz) : 6.77-8.28 (7H, m), 8.96 (1H, s). _________ 1.15 (3H, d, J=6.7Hz), 1.24 (3H, d, Cl J=6.7Hz), 2.28-2.42 (7H, m), 4.55 (1H, d, 51 0 C=O NS Isopropyl CH3 CH3 J=16. 4Hz), 4.97 (1H, d, J=16.4Hz), 253-254 6.94-6.96 (2H, m), 7.26 (1H, s), 7.35 (2H, s), 8.18 (1H, m), 9.29 (1H, s). _________ 0.96 (3H, t, J=7.5Hz), 2.05 (1H, m), 2.20-2.30 (7H, m), 2.40 (3H, s), 4.57 (1H, 52 O C=0 Ethyl CH3 CHs d, J=16.3Hz), 4.96 (1H, d, J=16.3Hz), 211-212 6.79-6.82 (2H, m), 7.24 (1H, s), 7.31 (2H, s), 8.29 (1H, d, J=4.6Hz), 9.55 (1H, s). ____ Table 3 (Continued) Ex A Z R1 R2 R3 R4 lH-NMR (200MHz, CDC13) 8 M. p. (8C) 0.97 (3H, t, J=7.4Hz), 2.02 (1H, m), H3C 2. 22-2. 31 (4H, m), 2.42 (3H, s), 4.56 (1H, 53 0 C=O N Ethyl CH3 F d, J=16.8Hz), 5.02 (1H, d, J=16.8Hz), 183-184 (5H, m), 8.30 (1H, m), _ 9. 64 (1H,s). __________________ 0.98 (3H, t, J=7. 5Hz), 2.10 (1H, m), 2. 25-2.32 (7H, m), 4.59 (1H, d, 54 O C=O -Ethyl CHs CHs J=15.6Hz), 4.96 (1H, d, J=15.6Hz), 217-218 . 6.94-6.97 (2H, m), 7.27 (1H, s), 7.33 (2H, s), 8.19 (1H, m), 9.34 (1H, s). __________ 1. 11 (3H, d, J=6.7Hz), 1.21 (3H, d, H3C J=6.7Hz), 2.22-2.38 (13H, m), 4.37 (1H, 55 O C=O Nk Isopropyl CH3 CH3 d, J=16. 0Hz), 5.05 (1H, d, J=16.0Hz), 232-233 6. 56 (2H, s), 7.19 (1H, s), 7.27 (2H, s), 9.70 (1H, s). __________________ 1.15 (3H, d, J=6.7Hz), 1.22 (3H, d, Hsc J=6.7Hz), 2.23 (1H, m), 2.36 (6H, s), 56 O C=O Nk Isopropyl F F 4.34 (1H, d, J=16.2Hz), 5.18 (1H, d, 176-178 J=1G. 2Hz), 6.58 (2H, s), 7.01-7.20 (3H, m), 9.25 (1H, s). _________________ 1.13 (3H, d, J=6.9Hz), 1.23 (3H, d, H3C (1H, m), 2.35 (6H, s), 172-173 57 O C=O Nk Isopropyl Cl Cl 4.22 (1H, d, J=16.3Hz), 5.30 (1H, d, J=1G. 3Hz), 6.54 (2H, s), 7.46 (2H, s), (foam) 7.50 (1H, s), 9.35 (1H, s). ____________ 1.12 (3H, d, J=6.7Hz), 1.22 (3H, d, H3C J=6.7Hz), 2.22-2.35 (10H, m), 4.35 (1H, 197-198 58 O C=O Nk Isopropyl CH2F CH3 d, J=lG. OHz), 5.13 (1H, d, J=16.0Hz), (for) H3C 5. 31 (2H, d, J=47.2Hz), 6.56 (2H, s), 7.37-7.50 (3H, m), 9.06 (1H, s). _________ 1.13 (3H, d, J=6.7Hz), 1.23 (3H, d, H3C J=6.7Hz), 2.20-2.35 (10H, m), 4.32 (1H, 59 O C=0 N. Cl CH3 d, J=16. 0Hz), 5.19 (1H, d, J=16. OHz), 222-223 H3C 6. 56 (2H, s), 7.27-7.50 (3H, m), 9.34 (1H. s). 0.95 (3H, t, J=7.5Hz), 2.02 (111, m), H3C 2.20-2.33 (13H, m), 4.45 (1Il, d, 60 0 C=O Nk Ethyl CH3 CH3 J=16. 0Hz), 5.05 (1H, d, J=16.0Hz), 211-212 HIC 6. 59 (2H, s), 7.22 (1H, s), 7.29 (21A, s), 9 45 (1H, s). _________________ Table 3 (Continued) Ex. A Z Rl R2 R3 R4 lH-NMR (200MHz, CDCl3) 8 M. p. (°C) 1.15 (3H, d, J=6.7Hz), I. 22 (3H, d, H3C J=6.7Hz), 2.23 (1H, m), 2. 3G (6H, s), 61 O C=0 N, Ethyl F F 4.34 (1H, d, J=16.2Hz), 5.18 (1H, d, 176-178 J=1G. 2Hz), 6.58 (2H, s), (3H, m), 9.25 (1H s). ________________ 1.14 (3H, d, J=6.7Hz), 1.23 (3H, d, NC J=6.7Hz), 2.30-2.40 (7H, m), 4.69 (1H, d, Isopropyl CH3 CH3 J=16.4Hz), 4.86 (1H, d, J=16.4Hz), 236-238 7.27-7.37 (5H, m), 8.52 (1H, m), 9.50 (1H, s). ___________________ 1.16 (3H, d, J=6.7Hz), 1.22 (3H, d, NC J=6. 7Hz), 2.30 (1H, m), 2.40 (3H, s) 63 O C=O N, 2H, s), 7. 27-7.56 (5H, m), 856 (1H, 220-221 d, J=5. lHz), 9.27 (1H, s). ____________ (CDC13/CD30D) a 1.11 (3H, d, J=7.1Hz), 1.23 (3H, d, J=7.1Hz), 64 O C=O N,-D/-Isopropyl CI-13 N02 2.23 (1H, m), 2.49 (3H, s), 4.63 (1H, d, 256-257 J=16. 2Hz), 4. 98 (1H, d, J=1G. 2Hz), 7.02 (2H, d, J=5.7Hz), 7.84 (1H, s), 8.27-8.35 (4H, m). ________________ 1.13 (3H, d, J=6.7Hz), 1.23 (3H, d, J=6.7Hz), 2.22 (1H, m), 2.37 (3H, s), H3c 2. 46 (3H, s), 4.41 (1H, d, J=16.2Hz),- 65 0 C=O N, Isopropyl CH3 NOz 5_25 (1H, d, J=16. 2Hz), G. 75-6. 79 (2H, 237-238 m), 7.76 (1H, s), 8.21-8.28 (3H, m), _ 9. 76 (1H,s). _________________

Example 66 : Synthesis of 1- (4'-picolyl)-5-isopropyl-6- (3', 5'-dimethylphenylamino)-2,4-pyrimidinedione (Compound 66) To a magnetically stirred DMF solution (10ml) of compound (II-a-1) obtained in Preparation 22 (630mg, 2mmol) at room temperature, were added anhydrous potassium carbonate (552mg, 4mmol), lithium iodide (268mg, 2mmol), and 4-picolyl chloride hydrochloride (328mg, 2mmol). After stirring for 24hr, the solvent was removed under reduced pressure and the resulting residue was purified by flash chromatography (eluent-ethyl acetate) to give 276mg (yield 34%) of 1- (4'-picolyl)-5-isopropyl-6- (3', 5'- dimethylphenylacetamido)-2,4-pyrimidinedione. The compound thus obtained was then refluxed in methanol (10ml) with sodium methoxide (llOmg, 2mmol) for 6hr. The reaction mixture was allowed to cool to room temperature and neutralized with excess ammonium chloride. The solvent was removed under reduced pressure and the resulting residue was purified by flash chromatography (eluent- methanol: ether=8: 92) to afford 280mg (yield 88%) of the title compound as a white solid.

M. p. : 272 to 273 °C 1H-NMR (200MHz, CDCl3) b 1.20 (6H, d, J=6.9Hz), 2.24 (6H, s), 2.90 (1H, m), 4.90 (2H, s), 6.27 (2H, s), 6.61 (1H, s), 7.04- 7.06 (2H, m), 8.42-8.45 (2H, m) m/z (EI) 364 (M+). <BR> <BR> <BR> <BR> <BR> <P>Example 67 : Synthesis of 1- (4'-picolyl)-5-ethyl-6- (3', 5'- dimethylphenylamino)-2,4-pyrimidinedione (Compound 67) The procedure of Example 66 was repeated using compound (II-a-2) obtained in Preparation 23 in place of compound (II-a-1) to prepare the title compound.

M. p. : 250 to 251 °C H-NMR (200MHz, CDCl3/CD30D) 6 0.99 (3H, t, J=7.5Hz), 2.24 (6H, s), 2.37 (2H, q, J=7.5Hz), 4.91 (2H, s), 6.31 (2H, s), 6.62 (1H,

s), 7.04-7.07 (2H, m), 8.40-8.43 (2H, m) m/z (EI) 350 (M+).

Example 68 : Synthesis of 1-(N-oxo-4'-picolyl)-5-isopropyl- 6- (3', 5'-dimethylbenzoyl)-2,4-pyrimidinedione (Compound 68) Compound 1 obtained in Example 1 (2.26g, 6mmol) was stirred with m-chloroperbenzoic acid (2.72g, 9mmol) in dichloromethane (120ml) at room temperature. After 6hr, the solvent was removed and the residue was purified by flash chromatography (eluent-chloroform: methanol=93: 7) to afford 2g (yield 84%) of the title compound as a white solid.

M. p. : 254 to 255 °C lH-NMR (200MHz, CDCl3) b 1.12 (3H, d, J=6.7Hz), 1.22 (3H, d, J=6.7Hz), 2.25-2.36 (7H, m), 4.69 (2H, s), 7.05-7.41 (5H, m), 8.05-8.09 (2H, m), 9.52 (1H, s) m/z (EI) 393 (M+).

Example 69 : Synthesis of 1-(N-oxo-3'-methyl-4'-picolyl)-5- <BR> <BR> <BR> <BR> isopropyl-6- (3', 5'-dimethylbenzoyl)-2,4-pyrimidinedione (Compound 69) Compound 45 obtained in Example 45 (834mg, 2.13mmol) was stirred with m-chloroperbenzoic acid (969mg, 3.2mmol) in dichloromethane (40ml) at room temperature. After 5hr, the solvent was removed and the residue was purified by flash chromatography (eluent-ethyl acetate: methanol=7: 1) to afford 860mg (yield 99%) of the title compound as a white solid.

M. p. : 223 to 224 °C lH-NMR (200MHz, CDCl3) 6 1.13 (3H, d, J=6.7Hz), 1.23 (3H, d, J=6.7Hz), 2.25-2.40 (10H, m), 4.56 (1H, d, J=16.0Hz), 4.85 (1H, d, J=16. OHz), 6.93 (1H, m), 7.31 (1H, s), 7.37 (2H, s), 8.10 (1H, m), 10.08 (1H, s) m/z (EI) 407 (M+).

Example 70 : Synthesis of 1-(N-oxo-3', 5'-dimethyl-4'-

picolyl)-5-isopropyl-6- (3', 5'-dimethylbenzoyl)-2,4- pyrimidinedione (Compound 70) Compound 55 obtained in Example 55 (840mg, 2mmol) was stirred with m-chloroperbenzoic acid (942mg, 3mmol) in dichloromethane (40ml) at room temperature. After 21hr, the solvent was removed and the residue was purified by flash chromatography (eluent-dichloromethane: methanol=15: 1) to afford 800mg (yield 95%) of the title compound as a white solid.

M. p. : 241 to 242 °C 1H-NMR (200MHz, CDCl3) 6 1.12 (3H, d, J=6.7Hz), 1.22 (3H, d, J=6.7Hz), 2.30-2.34 (13H, m), 4.41 (1H, d, J=16.0Hz), 4.98 (1H, d, J=16. OHz), 6.80 (2H, s), 7.27 (1H, s), 7.34 (2H, s), 9.21 (1H, s) m/z (EI) 421 (M+). <BR> <BR> <BR> <BR> <BR> <BR> <BR> <BR> <P>Example 71 : Synthesis of 1-(N-oxo-3', 5'-dimethyl-4'-<BR> <BR> <BR> <BR> <BR> <BR> picolyl)-5-isopropyl-6- (3'-chloro-5'-methylbenzoyl)-2,4- pyrimidinedione (Compound 71) Compound 59 obtained in Example 59 (860mg, 2mmol) was stirred with m-chloroperbenzoic acid (942mg, 3mmol) in dichloromethane (40ml) at room temperature. After 20hr, the solvent was removed and the residue was purified by flash chromatography (eluent-ethyl acetate: hexane=10: 1) to afford 870mg (yield 98%) of the title compound as a white solid.

M. p. : 225 to 226 °C 1H-NMR (200MHz, CDC13) 8 1.13 (3H, d, J=6.9Hz), 1.22 (3H, d, J=6.9Hz), 2.22-2.36 (10H, m), 4.39 (1H, d, J=16.0Hz), 5.04 (1H, d, J=16.0Hz), 6.80 (2H, s), 7.33-7.54 (3H, m), 9.14 (1H, s) m/z (EI) 441 (M+).

Example 72: Synthesis of 1- (3'-acetoxymethyl-4'-picolyl)-5- <BR> <BR> <BR> isopropyl-6- (3', 5'-dimethylbenzoyl)-2,4-pyrimidinedione

(Compound 72) Compound 69 obtained in Example 69 (800mg, 1.96mmol) was dissolved in acetic anhydride (10ml) and the solution was heated in an oil bath (120-140 °C) with stirring for 4hr. The solvent was then removed under reduced pressure and the residue was purified by flash chromatography (eluent -ethyl acetate: hexane=2: 1) to afford 150mg (yield 17%) of the title compound as a syrup.

1H-NMR (200MHz, CDC13) 6 1.14 (3H, d, J=6.7Hz), 1.28 (3H, d, J=6.7Hz), 2.16 (3H, s), 2.22-2.40 (7H, m), 4.68 (1H, d, J=16.2Hz), 4.88 (1H, d, J=16.2Hz), 5.08 (2H, s), 7.00-7.02 (2H, m), 7.26 (1H, s), 7.36 (2H, s), 8.44 (1H, m) m/z (EI) 449 (M+). <BR> <BR> <BR> <BR> <BR> <BR> <P>Example 73 : Synthesis of 1- (3'-acetoxymethyl-5'-methyl-4'-<BR> <BR> <BR> <BR> <BR> picolyl)-5-isopropyl-6- (3', 5'-dimethylbenzoyl)-2,4- pyrimidinedione (Compound 73) Compound 70 obtained in Example 70 (300mg, 0.71mmol) was dissolved in acetic anhydride (3ml) and the solution was heated in an oil bath (120-130 °C) with stirring for 2hr.

The solvent was then removed under reduced pressure and the residue was purified by flash chromatography (eluent-ethyl acetate: hexane=1: 1) to afford 110mg (yield 33%) of the title compound as a foam.

1H-NMR (200MHz, CDC13) 6 1.13 (3H, d, J=6.9Hz), 1.23 (3H, d, J=6.9Hz), 2.10-2.41 (10H, m), 4.53 (1H, d, J=16.0Hz), 4.96 (1H, d, J=16. OHz), 5.00 (2H, s), 6.78-6.81 (2H, m), 7.24 (1H, s), 7.34 (2H, s) m/z (EI) 463 (M+). <BR> <BR> <BR> <BR> <BR> <BR> <P>Example 74 : Synthesis of 1- (3'-acetoxymethyl-5'-methyl-4'-<BR> <BR> <BR> <BR> <BR> picolyl)-5-isopropyl-6- (3'-chloro-5'-methylbenzoyl)-2,4- pyrimidinedione (Compound 74) Compound 71 obtained in Example 71 (700mg, 1.58mmol)

was dissolved in acetic anhydride (10ml) and the solution was heated in an oil bath (120-130 °C) with stirring for 5hr. The solvent was then removed under reduced pressure and the residue was purified by flash chromatography (eluent -ethyl acetate: hexane=2: 1) to afford 115mg (yield 15%) of the title compound as a foam.

1H-NMR (200MHz, CDCl3) 1.14 (3H, d, J=6.9Hz), 1.24 (3H, d, J=6.9Hz), 2.16 (3H, s), 2.20-2.32 (4H, m), 2.42 (3H, s), 4.48 (1H, d, J=16.3Hz), 5.00 (2H, s), 5.06 (1H, d, J=16.3Hz), 6.76 (2H, d, J=5.9Hz), 7.32 (1H, s), 7.39 (1H, s), 7.52 (1H, s), 9.46 (1H, s) m/z (EI) 483 (M+).

Example 75: Synthesis of 1- (3'-hydroxymethyl-4'-picolyl)-5- <BR> <BR> <BR> isopropyl-6- (3', 5'-dimethylbenzoyl)-2,4-pyrimidinedione (Compound 75) Compound 72 obtained in Example 72 (lOOmg, 0.22mmol) was stirred with ammonium hydroxide (0.5ml) in methanol (5ml) at room temperature. After 6hr, the solvent was evaporated in vacuo and the resulting residue was recrystallized from methanol-chloroform to give 70mg (yield 77%) of the title compound as a white solid.

M. p. : 256 to 257 °C 1H-NMR (200MHz, DMSO-d6) 6 1.05 (3H, d, J=6.8Hz), 1.11 (3H, d, J=6.8Hz), 2.15 (1H, m), 2.28 (6H, s), 4.44 (2H, d, J=5.5Hz), 4.59 (1H, d, J=16.7Hz), 4.70 (1H, d, J=16.7Hz), 5.35 (1H, t, J=5.5Hz), 6.90 (1H, m), 7.15 (1H, s), 7.32 (1H, s), 7.55 (2H, s), 8.25 (1H, m), 11.66 (1H, s) m/z (EI) 407 (M+). <BR> <BR> <BR> <BR> <BR> <BR> <BR> <P>Example 76 : Synthesis of 1- (3'-hydroxymethyl-5'-methyl-4'- picolyl)-5-isopropyl-6- (3', 5'-dimethylbenzoyl)-2,4- pyrimidinedione (Compound 76) Compound 73 obtained in Example 73 (150mg, 0.32mmol) was stirred with ammonium hydroxide (0.5ml) in methanol

(5ml) at room temperature. After 5hr, the solvent was evaporated in vacuo and the resulting residue was recrystallized from methanol-chloroform to give 100mg (yield 74%) of the title compound as a white solid.

M. p. : 234 to 236 °C 1H-NMR (200MHz, DMSO-d6) 6 1.05 (3H, d, J=6.7Hz), 1.11 (3H, d, J=6.7Hz), 2.15 (1H, m), 2.26 (9H, s), 4.37 (2H, d, J=5.3Hz), 4.51 (1H, d, J=17.1Hz), 4.72 (1H, d, J=17.1Hz), 5.29 (1H, t, J=5.3Hz), 6.72 (1H, s), 6.93 (1H, s), 7.30 (1H, s), 7.51 (2H, s), 11.64 (1H, s) m/z (EI) 421 (M+). <BR> <BR> <BR> <BR> <BR> <BR> <BR> <P>Example 77 : Synthesis of 1- (3'-hydroxymethyl-5'-methyl-4'-<BR> <BR> <BR> <BR> <BR> <BR> picolyl)-5-isopropyl-6- (3'-chloro-5'-methylbenzoyl)-2,4- pyrimidinedione (Compound 77) Compound 74 obtained in Example 74 (lOOmg, 0.21mmol) was stirred with ammonium hydroxide (0.5ml) in methanol (5ml) at room temperature. After 6hr, the solvent was evaporated in vacuo and the resulting residue was recrystallized from methanol-chloroform to afford 78mg (yield 85%) of the title compound as a white solid.

M. p. : 238 to 240 °C 1H-NMR (200MHz, DMSO-d6) b 1.05 (3H, d, J=6.8Hz), 1.10 (3H, d, J=6.8Hz), 2.11 (1H, m), 2.27 (3H, s), 2.49 (3H, s), 4.37 (2H, d, J=5.7Hz), 4.47 (1H, d, J=17.1Hz), 4.82 (1H, d, J=17.1Hz), 5.27 (1H, t, J=5.7Hz), 6.75 (1H, s), 6.93 (1H, s), 7.56 (1H, s), 7.66 (1H, s), 7.74 (1H, s), 11.63 (1H, s) m/z (EI) 441 (M+).

Example 78: Synthesis of 1- (3'-methoxycarbonyl-4'-picolyl)- <BR> <BR> <BR> 5-isopropyl-6- (3', 5'-dimethylbenzoyl)-2,4-pyrimidinedione (Compound 78) Compound 62 obtained in Example 62 (lOOmg, 0.25mmol) was stirred with potassium carbonate (138mg, lmmol) and distilled water (0.5ml) in methanol (5ml) at room

temperature. After 18hr, the reaction mixture was acidified with glacial acetic acid and the solvent was evaporated in vacuo. The resulting residue was purified by flash chromatography (eluent-ethyl acetate: hexane=4: 1) to afford 74mg (yield 68%) of the title compound as a white solid.

M. p. : 138 to 140 °C 1H-NMR (200MHz, CDC13) b 1.14 (3H, d, J=6.9Hz), 1.23 (3H, d, J=6.9Hz), 2.28-2.38 (7H, m), 3.98 (3H, s), 4.68 (1H, d, J=16.0Hz), 5.00 (1H, d, J=16.0Hz), 7.21-7.33 (4H, m), 7.73 (1H, s), 8.54 (1H, m), 9.45 (1H, s) m/z (EI) 435 (M+). <BR> <BR> <BR> <BR> <BR> <P>Example 79 : Synthesis of 1- (3'-carbamoyl-4'-picolyl)-5-<BR> <BR> <BR> isopropyl-6- (3', 5'-dimethylbenzoyl)-2,4-pyrimidinedione (Compound 79) Compound 62 obtained in Example 62 (60mg, 0.15mmol) was stirred with conc. sulfuric acid (1ml) in an oil bath (80 °C). After 10min, the reaction mixture was allowed to cool to room temperature and poured into distilled water (10ml).

The resulting precipitate was collected by filtration, washed with distilled water and hexane, and dried in vacuo to afford 38mg (yield 61%) of the title compound as a white solid.

M. p. : 295 to 296 °C 1H-NMR (500MHz, DMSO-d6) 6 1.03 (3H, d, J=6.9Hz), 1.10 (3H, d, J=6.9Hz), 2.14 (1H, m), 2.25 (6H, s), 4.67 (1H, d, J=17.6Hz), 4.75 (1H, d, J=17. 6Hz), 7.26 (1H, dd, J=5. 0Hz, J=1.7Hz), 7.29 (1H, s), 7.53 (2H, s), 7.63 (1H, d, J=2.5Hz), 7.69 (1H, s), 8.04 (1H, d, J=2.1Hz), 8.40 (1H, d, J=5.0Hz), 11.71 (1H, s) m/z (EI) 420 (M+). <BR> <BR> <BR> <BR> <BR> <P>Example 80 : Synthesis of 1- (3'-carbamoyl-4'-picolyl)-5-<BR> <BR> <BR> <BR> isopropyl-6- (3'-chloro-5'-methylbenzoyl)-2,4-pyrimidinedione (Compound 80) Compound 63 obtained in Example 63 (90mg, 0.21mmol) was

stirred with conc. sulfuric acid (1ml) in an oil bath (80 °C). After 10min, the reaction mixture was allowed to cool to room temperature and poured into distilled water (10ml).

The resulting precipitate was collected by filtration, washed with distilled water and hexane, and dried in vacuo to afford 87mg (yield 92%) of the title compound as a white solid.

M. p. : 284 to 285 °C 1H-NMR (500MHz, DMSO-d6) 6 1.03 (3H, d, J=6.8Hz), 1.10 (3H, d, J=6.8Hz), 2.12 (1H, m), 2.29 (3H, s), 4.68 (1H, d, J=17.3Hz), 4.76 (1H, d, J=17.3Hz), 7.29 (1H, dd, J=5. OHz, J=1.7Hz), 7.58 (1H, s), 7.63 (1H, d, J=2.5Hz), 7.71 (1H, s), 7.74 (1H, s), 7.80 (1H, s), 8.04 (1H, d, J=2.5Hz), 8.41 (1H, d, J=5. OHz), 11.72 (1H, s) m/z (EI) 440 (M+).

Example 81 : Synthesis of 1- (4'-aminobenzyl)-5-isopropyl-6- (3', 5'-dimethylbenzoyl)-2,4-pyrimidinedione (Compound 81) Compound 38 obtained in Example 38 (50mg, 0.12mmol) in methanol (5ml) was stirred under an atmosphere of hydrogen in the presence of platinium oxide catalyst (l0mg) at room temperature for 4hr. The reaction mixture was filtered through celite and the solvent was removed under reduced pressure. The resulting residue was purified by flash chromatography (eluent-ethyl acetate: hexane=1: 1) to afford 32mg (yield 70%) of the title compound as a yellow solid.

M. p. : 173 to 175 °C 1H-NMR (200MHz, CDC13) 6 1.07 (3H, d, J=6.9Hz), 1.20 (3H, d, J=6.9Hz), 2.20-2.40 (7H, m), 3.57 (2H, s), 4.46 (1H, d, J=15.2Hz), 5.00 (1H, d, J=15.2Hz), 6.35 (2H, d, J=8.3Hz), 6.81 (2H, d, J=8.3Hz), 7.21 (1H, s), 7.26 (2H, s), 8.86 (1H, s) m/z (EI) 391 (M+).

Antiviral Activity and CytotoxicitY Test The in vitro anti-HIV-1 assays were based on the inhibition of the virus-induced cytopathic effect in MT-4 cells, as described in J. Med. Chem, 34,349 (1991).

First, MT-4 cells were suspended in a culture medium at a concentration of 1 x 104 cells/ml and infected with 500 TCID50 (50% cell culture infective dose)/well of HIV-1.

Immediately after the virus infection, 100 pu of the cell suspension was added to each of the wells of a flat-bottomed microtiter tray containing various concentrations of the test compounds (1) to (81). After incubating for 4 or 5 days at 37 °C, the number of viable cells was determined by the 3- (4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) method, as disclosed in J. Virol. Methods, 20,309 (1988).

The cytotoxicity of the compounds of the present invention was assessed in parallel with their antiviral activity. It was based on the viability of mock-infected host cells as determined by the MTT method (see J. Virol.

Methods, 20,309 (1988)). MKC-442 (6-benzyl-1-ethoxymethyl- 5-isopropyluracil) was employed as a comparative compound.

The results of the tests are shown in Table 4.

Table 4 Ex. No. (Compound) CD50(µg/ml)* ED50(µg/ml)** S. I. (CDso/ED5o)*** 1 22. 6 0.0026 8,600 2 27. 2 0. 0036 7,578 3 26. 1 0.0055 4,788 4 64. 0 0. 0027 23,940 5 18. 7 0. 012 1,553 6 28. 2 0. 0127 2,215 7 22. 7 0. 0034 6,597 8 28. 16 0. 008 3,451 9 40. 5 0. 0119 3,401 10 51.7 0.0101 5,133 11 47. 4 0. 0178 2,658 12 38. 9 0. 0542 716 13 42. 3 0. 0124 3,414 14 29. 81 0. 049 612 15 49. 87 0. 053 943 16 50. 6 O. OôO1 841 177430. 112663 18 93. 2 0. 1189 784 19 11. 28 0. 003 3,394 20 32. 9 0. 012 2,758 21 55. 07 0. 0023 23,501 22 92. 8 0. 002 48,305 MKC-442 27.7 0. 005 5,544 Foot note : CD50 Cytotoxic concentration that causes death of MT-4 cells by 50 % ED50 Effective concentration for the inhibition of the proliferation of HIV-1 by 50% S. I.: Selectivity index = (CDso/ED50) Table 4 (Continued) Ex. No. (Compound) CD50(µg/ml)* ED50(µg/ml)** S.I. (CD50/ED50)*** 23 52. 1 0. 003 15,245 24 15. 8 0. 010 1,628 25 >100 0. 018 >5,557 26 6. 5 0. 003 2,112 27 8. 5 0. 002 5,747 28 12. 5 0. 004 3, 510 29 44. 9 1. 867 24 30 52. 3 1. 935 27 31 11. 7 1. 8 6 32 40. 4 0. 003 12,039 33 57. 1 0. 011 5, 073 34 37. 4 0. 014 2,663 35 >100 O. OõOõ >1,650 36 8. 01 0. 004 2,170 37 5. 78 0. 003 2, 066 38 5. 65 0. 005 1,172 39 7. 46 0. 003 2,654 40 7. 97 0. 0348 229 41 4. 63 0. 009 497 42 2. 14 0. 002 921 43 7. 16 0. 0035 2,057 44 8. 17 1. 80 5 MKC-442 27. 7 0. 005 5,544 Foot note: * CD50 : Cytotoxic concentration that causes death of MT-4 cells by 50 % ED50 : Effective concentration for the inhibition of the proliferation of HIV-1 by 50% S. I.: Selectivity index = (CD50/ED50) Table 4 (Continued) Ex. No CD50(µg/ml)* ED50(µg/ml)** S.I. (CD50/ED50)*** (Compound) 45 >100 0.0098 >10,170 46 22.9 0.0024 9,691 47 93.75 0.0027 35,133 48 12.07 0.0030 4,021 49 64. 39 0.0076 8,440 50 47.68 0.0029 16,351 51 17. 1 0. 0010 17,812 52 14.3 0.0010 14, 684 53 37. 8 0. 0031 12,110 54 8. 7 0. 0017 4,992 55 9. 9 0. 0010 10,274 56 87.2 0.004419,648 57 9.46 0.0028 3,411 58 36. 03 0.0025 14,300 59 8. 68 0. 0021 4, 126 60 17.5 0.0026 6,739 61 37.5 0.0151 2,475 62 9.15 0.001ô 5,858 63 8. 55 0. 0029 2, 966 64 46 0. 0096 4,801 65 44. 08 0. 0075 5,916 60 >100 0.08 >1,287 MKC-442 27. 7 0. 005 5,544 Foot note: * CDn : Cytotoxic concentration that causes death of MT-4 cells by 50 % ED50 Effective concentration for the inhibition of the proliferation of HIV-1 by 50% S. S. I.: Selectivity index = (CD50/ED50) Table 4 (Continued) Ex. No. (Compound) CD50(µg/ml)* ED50(µg/ml)** S.I. (CD50/ED50)*** 67 54. 5 0. 42 130 68 56.9 0. 0145 3,928 69 48.25 0.0125 3,853 70 25. 84 0. 0055 4,712 71 25. 44 0. 0082 3,092 72 38. 49 0. 0088 4,365 73 39.65 0. 0067 5,903 74 28.81 0. 0134 2,152 75 42.00 0. 0031 13,444 76 38. 39 0. 0084 4, 561 77 23.51 0. 0115 2,052 78 40. 79 0. 0075 5,414 79 >100 0. 0091 >10,942 80 27.83 0. 0111 2,507 81 9. 63 0. 015 648 MKC-442 27. 7 0. 005 5,544 Foot note: * CD50 : Cytotoxic concentration that causes death of MT-4 cells by 50 %<BR> <BR> <BR> ED50 Effective concentration for the inhibition of the<BR> <BR> <BR> proliferation of HIV-1 by 50%<BR> <BR> <BR> S. I.: Selectivity index = (CD50/ED50)

Antiviral activity acrainst mutant HIV-1 Antiviral activities of the inventive compounds were determined against Y181C which is representative HIV-1 mutant having high resistance against anti-HIV-1 nonnucleosides, e. g., Nevirapine, by the MTT method. MKC- 442 was employed as a comparative compound.

The representative results of the tests are shown in Table 5.

Table 5 Compound EC50 (yM) * 1 0.005-0.014 4 0.010-0.041 MKC-442 13. 4 Foot note: ECSO : Effective concentration for the inhibition of the proliferation of mutant HIV-1 by 50% Reference : J. Med. Chem., 42,4500 (1999) As the above results show, the novel antiviral 2,4- pyrimidinedione derivatives of the present invention possess high antiviral activity against HIV-1, both wild-type and mutant HIV-1, and at the same time show high selectivity indices, i. e., low toxicity. The inventive compounds can therefore be used as a drug for treating AIDS.

While the invention has been described with respect to the specific embodiments, it should be recognized that various modifications and changes may be made by those skilled in the art to the invention which also fall within the scope of the invention as defined by the appended claims.