AU729341B2 - Hydantoin derivatives having an inhibitory activity for farnesyl transferase - Google Patents

Hydantoin derivatives having an inhibitory activity for farnesyl transferase Download PDF

Info

Publication number
AU729341B2
AU729341B2 AU84647/98A AU8464798A AU729341B2 AU 729341 B2 AU729341 B2 AU 729341B2 AU 84647/98 A AU84647/98 A AU 84647/98A AU 8464798 A AU8464798 A AU 8464798A AU 729341 B2 AU729341 B2 AU 729341B2
Authority
AU
Australia
Prior art keywords
methyl
imidazol
naphthalen
dioxo
propyl
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
AU84647/98A
Other versions
AU8464798A (en
Inventor
Hyun Ho Chung
Won Hee Jung
Jong Hyun Kim
Sang Woong Kim
Jong Sung Koh
Tae Hwan Kwak
Hyun Il Lee
Jin Ho Lee
Kyung Duk Moon
Ki Won Park
Seong Gu Ro
You Seung Shin
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
LG Corp
Original Assignee
LG Chemical Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by LG Chemical Co Ltd filed Critical LG Chemical Co Ltd
Publication of AU8464798A publication Critical patent/AU8464798A/en
Application granted granted Critical
Publication of AU729341B2 publication Critical patent/AU729341B2/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/66Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D233/72Two oxygen atoms, e.g. hydantoin
    • C07D233/74Two oxygen atoms, e.g. hydantoin with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to other ring members
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/02Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/66Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D233/72Two oxygen atoms, e.g. hydantoin
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/66Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D233/72Two oxygen atoms, e.g. hydantoin
    • C07D233/76Two oxygen atoms, e.g. hydantoin with substituted hydrocarbon radicals attached to the third ring carbon atom
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D277/00Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/02Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
    • C07D277/20Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D277/22Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D333/00Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
    • C07D333/02Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
    • C07D333/04Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
    • C07D333/06Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring carbon atoms
    • C07D333/24Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/06Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/14Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Public Health (AREA)
  • General Chemical & Material Sciences (AREA)
  • Immunology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Rheumatology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)

Description

WO 99/05117 PCT/KR98/00225 -1- HYDANTOIN DERIVATIVES HAVING AN INHIBITORY ACTIVITY FOR FARNESYL TRANSFERASE TECHNICAL FIELD The present invention relates to a novel hydantoin derivative represented by the following formula which shows an inhibitory activity against farnesyl transferase, and thus can be used as an effective therapeutic agent against anti-proliferative diseases, such as resfenosis, Rheumatitis arthrititis and particularly cancer: [Formula I] O R2 R3N NP 0 or pharmaceutically acceptable salts thereof, in which R 1
R
2
R
3 and R 4 are defined as described below.
The present invention also relates to a process for preparation of the compound of formula and to an anti-cancer composition comprising the compound of formula as an active ingredient.
BACKGROUND ART Mammalian Ras proteins act as molecular switches in the signalling events associated with cell growth and differentiation. The ras proto-oncogene family consists of three members, and H-ras, which code for highly homologous four types of proteins; N-ras WO 99/05117 PCT/KR98/00225 2 proteins of 189 residues and two isomorphic K-ras-4B and K-ras-4A proteins of 188 and 189 residues, respectively. The chemical basis for the switch mechanism involves cycling of the protein between the inactive (off) guanosine diphosphate (GDP) bound state and the active (on) guanosine triphosphate (GTP) bound state (Bourne, Sanders, McCormick, Nature, 1991, 349,117). Biochemical and structural studies have shown that point mutations of the residues 12, 13, and 61, positioned in the neighborhood of phosphoryl group of GTP, resulting in the decrease of guanosine triphosphatase activity are associated with many human cancers, particularly, pancreatic cancer, urinary bladder carcinoma, colon cancer, etc. (Bos, Cancer Res., 1989, 49, 4682).
Ras protein is synthesized as a cytosolic precursor that is ultimately localized to the cytoplasmic face of the plasma membrane after a series of posttranslational modification (Gibbs, Cell 1991, These series of biochemical modifications, by changing the electrical charge state or spacial structure to increase the hydrophobicity allow Ras protein to attach to cell membrane more easily. The first and obligatory step in the series is the addition of a farnesyl moiety to the cysteine residue of the C-terminal CAAX motif cysteine; A, usually aliphatic residue; X, any other amino acid) in a reaction catalyzed by farnesyl protein transferase (FTase). This modifications is essential for Ras function, as demonstrated by the inability of Ras mutants lacking the C-terminal cysteine to be farnesylated, to localize to the plasma, and to transform mammalian cells in culture (Hancock, Magee, Child, Marshall, Cell 1989, 57, 1167). The subsequent posttranslational modifications, cleavage of the AAX residues, carboxyl methylation of the farnesylated cysteine, and palmitoylation of the cysteines located upstream of the CAAX motif in H-and N-ras proteins WO 99/05117 PCT/KR98/00225 3 are not obligatory for Ras membrane association or cellular transforming activity. Interestingly, K-ras-4B, different from H- and N-ras, has a multiple lysine rich region named polybasic domain, instead of having cysteine required for palmitoylation, thereby facilitating the farnesylated ras protein to bind to anionic lipid layer of cell membrane. The inhibitors of FTase that catalyzes the obligatory modification have therefore been suggested as anticancer agents for tumors in which Ras oncogene contributes to transformation (Buses, J.E. et al., Chemistry Biology, 1995, 2 787). A number of FTase inhibitors have recently identified demonstrated potent and specific ability to block Ras farnesylation, signalling and transformation in transformed cells and tumor cell lines both in vitro and in animal models (Koh, N.E. et al., Proc.
Natl. Acad. Sci. USA, 1994, 91, 914; Kohl, N.E. et al., Nature Medicine, 1995, 1 792). However, most of the inhibitors are related to CAAX motif as Ras substrate mimic and peptidie in nature or contain a sulfhydryl group (US Patent No. 5,141,851; Kohl, N.E. et al., Science, 1993, 260, 1934; PCT/US95/12224, Graham et al.; Sebti, S.M. et al., J.
Biol. Chem., 1995, 270, 26802; James, G.L. et al., Science, 1993, 260, 1937; Bishop, W.R. et al., J. Biol. Chem., 1995, 270, 30611). Recently, a new type of peptidomimetic inhibitor imitating catalytic step of FTase has been reported (Poulter, C.D. et al., J.Am. Chem. Soc., 1996, 118,8761). The chemical basis of the inhibitor design relates to the reaction mechanism. That is, transferring prenyl group by the enzyme is electrophilic displacement and the reaction requires charge in a transition state.
These inhibitors previously described however possess limited activity and selectivity for inhibition of the oncogenic function of Ras proteins, particularly K-ras-4B, which is found to be most common in human cancer. Therefore, new inhibitor having the ability of effectively inhibiting K-ras activity is required.
Disclosure of Invention The present inventors have performed studies for developing a compound having the structure characteristics imitating transition state of catalytic reaction of farnesyl transferase and as a result, found that hydantoin derivatives according to the present invention can inhibit farnesyl transferase activity by imitating transition state of catalytic reaction of farnesyl transferase.
Therefore, the object of the present invention is to provide a hydantoin derivative of formula which inhibits the activity of farnesyl transferase, process for preparation thereof, and anti-cancer composition comprising the compound of formula as an active component.
Best Mode for Carrying out the Invention According to a first aspect, the present invention consists in a hydantoin derivative represented by the following formula [Formula I] O R, R2
N
O
*0 0 or pharmaceutically acceptable salt thereof in which R, and R 2 independently of one another represent hydrogen; lower alkyl; monocyclic or bicyclic aryl group which can be substituted by lower alkyl or halogen; heterocyclic 20 group containing hetero atoms selected from a group consisting of nitrogen and sulfur as .o ring member; or a radical having the following formula: 0 m D m (wherein D represents alkoxy; hydroxy; amino acid residue; morpholine; thiomorpholine; piperazine, alkoxyalkylamine or aryloxyalkylamine each of which is substituted or unsubstituted by lower alkyl, and m is selected from 0 to 2),
R
3 represents amino acid residue; or a radical having the following formula, [R:\LIBFF]0913speci.doc:njc S[R:\LIBFF]09131 speci.doc:njc A
A
BN B
N
N
N
C
C
wherein A represents hydrogen; lower alkyl; aryl group which is substituted by substituents selected from a group consisting of halogen, cyano(CN), nitro(N0 2 carboxy(COOH), amide, thioamide, SR and lower alkyl; heterocyclic group which is substituted by substituents selected from a group consisting of halogen, cyano, nitro, COOR, amide, thioamide, SR and lower alkyl and which comprises nitrogen or sulfur atom as ring member; lower alkyl substituted by the substituted aryl or heterocyclic group as mentioned above; or a radical having the following formula: N E (in the definition for the substituent A, R represents hydrogen or lower alkyl, and E "represents hydrogen or -F-G wherein F represents CH 2 C=0, SO 2 and G represents hydrogen; lower alkyl substituted or unsubstituted by phenyl or biphenyl; lower alkoxy; phenyl; benzyl; benzyloxy; amine substituted or unsubstituted by lower alkyl, phenyl, benzyl, cycloalkyl or phenoxy alkyl), B and C independently of one another represent hydrogen, halogen or lower alkyl, n denotes an integer of 0 to 4,
R
4 represents hydrogen; aromatic group substituted or unsubstituted by lower alkyl or 20 halogen; bicyclic aromatic group; heteroaromatic group containing hetero atoms selected form a group consisting of nitrogen and sulfur as ring member; or a radical having the following formula: [R:\LIBFF]09131 speci.doc:njc n R5 N
N
H H ii N X I ,n N 6 OR 9
H
n 0 R7 R7 H R 8 H R 8 R7 R. "R OR9 R8
R
6 R OR
R
6
X
wherein R represents aryl group substituted by lower alkoxy; or heterocyclic group containing .***bhetero atoms selected from a group consisting of nitrogen, oxygen and sulfur as ring member, o R 6 represents hydrogen; lower alkyl; lower alkyl which is substituted by substituents selected from a group consisting of halogen, cyano, hydroxy, COOR, amide, thioamide, SR and SO 2 R; lower alkyl substituted by an aryl group which is substituted by substituents selected from a group consisting of halogen, cyano, COOR, amide, thioamide, SR, SO 2 R and lower alkyl; heterocyclic group containing hetero atoms selected from a group consisting of nitrogen and sulfur as ring member; heterocyclic group which is substituted by substituents selected from a group consisting of halogen, s cyano, COOR, amide, thioamide, SR, SO 2 R and lower alkyl and which contains hetero [R:\LIBFF]0913 Ispeci.doc:njc 4c atoms selected from a group consisting of nitrogen and sulfur as ring member, wherein R represents lower alkyl,
R
7 and R 8 independently of one another represent hydrogen, halogen, halogenoalkyl, cyano, amide, thioamide, alkoxy or phenoxy, or represent a radical having the following formula, 0 S--C-N Z-Rjo c 7n Rio 0
RIO
-C-N Zwherein Z represents CH 2 CO, 0, S, SO 2
NR
9
NHSO
2 or NHCOO, Rio represents hydrogen, lower alkyl, halogenoalkyl, alkoxy, hydroxy, benzyloxycarbonyl or benzyl,
R
9 represents hydrogen or lower alkyl, or lower alkyl substituted by aromatic group, X represents C1l 2 CO, 0, S or SO 2 and n denotes an integer of 0 to 4.
ti5 According to a second aspect, the present invention consists in a process for preparing a hydantoin derivative of formula as defined in the first aspect wherein 1) a compound represented by the following formula (II): [Formula II] 0 R, NH N 0 20 wherein RI, R 2 and R4 are as defined in the first aspect, is reacted under Mitsunobu reaction condition with an alcohol derivative represented by the following formula (III): [Formula III]
R
3
-OH
.wherein R 3 is as defined in the first aspect, or [R:\LIBFF]0913 1speci.doc:njc 4d 2) a compound represented by the following formula (IIa): [Formula IIa] wherein R, and R 2 are defined as previously described, is reacted with the alcohol derivative of formula (III) under Mitsunobu reaction condition to produce a compound represented by the following formula (Ia): [Formula la] 0
R,
R3 N NH R< W' o *f ooo, o wherein R 1
R
2 and R 3 are defined as previously described, then substituent R4, is 10 introduced into the resulting compound of formula (la) to produce a compound represented by the following formula (Ib): [Formula Ib] O
R,
R3 N Y N R4 0 wherein R 1
R
2 and R 3 are defined as previously described and R 4 is the same as R4 except that R 4 is not hydrogen.
According to a third aspect, the present invention consists in an anti-cancer composition comprising the compound of formula as defined in the first aspect or prepared by the process of the second aspect or a pharmaceutically acceptable salt thereof as an active ingredient together with a pharmaceutically acceptable carrier.
[R:\LIBFF]09131 speci.doc:njc 4e According to a fourth aspect, the present invention consists in a method for the treatment or prophylaxis of an anti-proliferative disease comprising administering to a patient in need of such treatment or prophylaxis a therapeutically effective amount of a hydantoin derivative according to the first aspect, a hydantoin derivative prepared by the s process of the second aspect or a composition according to the third aspect.
According to a fifth aspect, the present invention consists in use of a hydantoin derivative according to the first aspect or prepared by the process of the second aspect in the manufacture of a medicament for the treatment or prophylaxis of an anti-proliferative disease.
According to a sixth aspect, the present invention consists in a hydantoin derivative according to the first aspect or prepared by the process of the second aspect when used for the treatment or prophylaxis of an anti-proliferative disease.
The present invention provides a hydantoin derivative represent by the following formula and pharmaceutically acceptable salt thereof which inhibit the activity of farnesyl transferase: [Formula I] 0 R, N
N
R30 N R4 in which 0.4 *0 .00.* [R:\LIBFF]09131 speci.doc:njc WO 99/05117 PCT/KR98/00225 5 R, and R 2 independently of one another represent hydrogen; lower alkyl; monocyclic or bicyclic aryl group which can be substituted by lower alkyl or halogen; heterocyclic group containing hetero atoms selected from a group consisting of nitrogen and sulfur as ring member; or a radical having the following formula: 0 (wherein D represents alkoxy; hydroxy; amino acid residue; morpholine; thiomorpholine; piperazine, alkoxyalkylamine or aryloxyalkylamine each of which is substituted or unsubstituted by lower alkyl, and m is selected from 0 to 2),
R
3 represents amino acid residue; or a radical having the following formula, A
A
B
B
N N Nr
N
wherein A represents hydrogen; lower alkyl; aryl group which is substituted by substituents selected from a group consisting of halogen, cyano(CN), nitro(N02), carboxy(COOH), amide, thioamide, SR and lower alkyl; heterocyclic group which is substituted by substituents selected from a group consisting of halogen, cyano, nitro, COOR, amide, thioamide, SR and lower alkyl and which comprises nitrogen or sulfur atom as ring member; lower alkyl substituted by the substituted aryl or heterocyclic group as mentioned above; or a radical having the following formula: WO 99/05117 PCT/KR98/00225 6
N-E
(in the definition for the substituent A, R represents hydrogen or lower alkyl, and E represents hydrogen or -F-G wherein F represents CH 2 C=O, SO 2 and G represents hydrogen; lower alkyl substituted or unsubstituted by phenyl or biphenyl; lower alkoxy; phenyl; benzyl; benzyloxy; amine substituted or unsubstituted by lower alkyl, phenyl, benzyl, cycloalkyl or phenoxy alkyl), B and C independently of one another represent hydrogen, halogen or lower alkyl, n denotes an integer of 0 to 4, R4 represents hydrogen; aromatic group substituted or unsubstituted by lower alkyl or halogen; bicyclic aromatic group; heteroaromatic group containing hetero atoms selected from a group consisting of nitrogen and sulfur as ring member; or a radical having the following formula: WO 99/05117 PCT/KR98/00225 -7- O o R, NE' R6NH'
RR
oOR x x wherein Rs represents aryl group substituted by lower alkoxy; or heterocyclic group containing hetero atoms selected from a group consisting of nitrogen, oxygen and sulfur as ring member, R6 represents hydrogen; lower alkyl; lower alkyl which is substituted by substituents selected from a group consisting of halogen, cyano, hydroxy, COOR, amide, thioamide, SR and SO 2 R; lower alkyl substituted by an aryl group which is substituted by substituents selected from a group consisting of halogen, cyano, COOR, amide, thioamide, SR, SO 2
R
and lower alkyl; heterocyclic group containing hetero atoms selected from a group consisting of nitrogen and sulfur as ring member; heterocyclic group which is substituted by substituents selected from a group consisting of halogen, cyano, COOR, amide, thioamide, SR, SO 2 R and lower alkyl and which contains hetero atoms selected from a group consisting of nitrogen and sulfur as ring member, wherein R represents WO 99/05117 PCT/KR98/00225 -8lower alkyl,
R
7 and R8 independently of one another represent hydrogen, halogen, halogenoalkyl, cyano, amide, thioamide, alkoxy or phenoxy, or represent a radical having the following formula, /4-nN R Z-N Z-RIO C-N Zwherein Z represents CH 2 CO, 0, S, SO02, NR 9
NHSO
2 or NHCOO, Rio represents hydrogen, lower alkyl, halogenoalkyl, alkoxy, hydroxy, benzyloxycarbonyl or benzyl,
R
9 represents hydrogen or lower alkyl, or lower alkyl substituted by aromatic group, X represents CH 2 CO, 0, S or SO02, and n denotes an integer of 0 to 4.
In the definitions for the substituents of the compound of formula the term "lower alkyl" means a straight or branched alkyl having 1 to 4 carbon atoms which includes methyl, ethyl, isopropyl, isobutyl and t-butyl; the term "heterocyclic group containing hetero atoms selected from a group consisting of nitrogen and sulfur as ring member" means mono- or bicyclic aliphatic or aromatic group containing one or two nitrogen or sulfur in the ring as ring member.
The abbreviations for amino acids used in the present specification are consistent with IUPAC-IUB Commission on biochemical nomenclature of amino acid and peptide[Eur. J Biochem., 1984, 158, 9-31].
Also, the compound of formula according to the present invention can form a pharmaceutically acceptable salt. Such salt includes WO 99/05117 PCT/KR98/00225 9 non-toxic acid addition salt containing pharmaceutically acceptable anion, for example a salt with inorganic acids such as hydrochloric acid, sulfuric acid, nitric acid, phosphoric acid, hydrobromic acid, hydriodic acid, etc., a salt with organic carboxylic acids such as tartaric acid, formic acid, citric acid, acetic acid, trichloroacetic acid, trofluoroacetic acid, gluconic acid, benzoic acid, lactic acid, fumaric acid, maleic acid, etc., or a salt with sulfonic acids such as methanesulfonic acid, benzenesulfonic acid, p-toluenesulfonic acid, naphthalenesulfonic acid, etc.; and metal addition salt for example a salt with alkali metal or alkaline earth metal such as lithium salt. Further, the present invention includes a solvate of the compound of formula such as alcoholate, and hydrate thereof.
Since the compound of formula according to the present invention may have asymmetric carbon atoms depending on the substituents, they can be present in the form of racemate, diastereomer mixture or the individual diastereomers. Thus, the present invention also includes all of these stereoisomers and their mixtures.
Among the compound of formula according to the present invention, the preferred compounds include those wherein Ri represents hydrogen; monocyclic or bicyclic aryl group which can be substituted by lower alkyl or halogen; or a radical having the following formula: 0 (wherein D represents alkoxy; hydroxy; amino acid residue; morpholine; thiomorpholine; piperazine or alkoxyalkylamine each of which is substituted or unsubstituted by lower alkyl, and m is selected from 0 to 1), WO 99/05117 PCT/KR98/00225 10 R2 represents hydrogen; lower alkyl; or a radical having the following formula: o (wherein D represents alkoxy; hydroxy; amino acid residue; morpholine; thiomorpholine; piperazine or alkoxyalkylamine each of which is substituted or unsubstituted by lower alkyl, and m is selected from 0 to 1), R3 represents a radical having the following formula, A
A
C N C wherein A represents hydrogen; aryl group which is substituted by substituents selected from a group consisting of halogen, cyano(CN), nitro(N02), carboxy(COOH), amide, thioamide, SR and lower alkyl; or a radical having the following formula:
-CN-E
(in the definition for the substituent A, R represents hydrogen or lower alkyl, and E represents hydrogen or -F-G wherein F represents C=0, and G represents benzyloxy, lower alkoxy, or lower alkyl substituted or unsubstituted by phenyl), B and C independently of one another represent hydrogen, n denotes an integer of 1 to 3, R4 represents hydrogen; aromatic group substituted or unsubstituted by halogen; bicyclic aromatic group; heteroaromatic group containing hetero atoms selected from a group consisting of nitrogen and sulfur as ring WO 99/05117 PCT/KR98/00225 11 member; or a radical having the following formula: 0 0
R
R NH' N N OR 9
R
6 0
R
8 0 OR X RR 9 wherein
R
5 represents aryl group substituted by lower alkoxy; or heterocyclic group containing hetero atoms selected from a group consisting of nitrogen, oxygen and sulfur as ring member, R6 represents hydrogen; lower alkyl; lower alkyl which is substituted by substituents selected from a group consisting of halogen, cyano, hydroxy, COOR, amide, thioamide, SR and SO 2 R; lower alkyl substituted by an aryl group which is substituted by substituents selected from a group consisting of halogen, cyano, COOR, amide, thioamide, SR, SO 2
R
and lower alkyl; or heterocyclic group containing hetero atoms selected from a group consisting of nitrogen and sulfur as ring member; heterocyclic group which is substituted by substituents selected from a group consisting of halogen, cyano, COOR, amide, thioamide, SR, SO 2
R
and lower alkyl and which contains hetero atoms selected from a group consisting of nitrogen and sulfur as ring member, wherein R represents lower alkyl,
R
7 and Rs independently of one another represent hydrogen, halogen, halogenoalkyl, cyano or phenoxy, or represent a radical having the WO 99/05117 PCT/KR98/00225 12 following formula, n'Rio 0 -P-N o
RIO-
-j-C-N Z-
T
wherein Z represents 0, S, SO 2
NR
9
NHSO
2 or NHCOO, Rio represents hydrogen, lower alkyl, halogenoalkyl, alkoxy, hydroxy or benzyloxycarbonyl, R9 represents hydrogen or lower alkyl, X represents 0, S or SO 2 and n denotes an integer of 1 to 3.
Typical examples of the compound of formula according to the present invention are presented in the following Tables la to Iv.
WO 99/05117 WO 9905117PCT/KR98/00225 13 Table la COM. Formula INomenclature
NO.
Ir- 0O-I o 1-yl-2,4-dioxo-imidazolidin-l-y 1'1_N YN~)N OCH 3 I)}-acetylamino)-4-methyl sulfan 0 0 yl-butyric acid methyl ester 2-(2-f 1H-imidazol-4-yl)- Ipropyl 5-m ethyl -5-naphthal en- 2 0 1-yl-2,4-dioxo-imidazolidin-1-y HN N YN~JN OH 11-acetylamino)-4-methyl sul fan 0o yl-butyric acid 2-(2-{3-[2-(1H-imidazol-4-yl)-e Ithyl ethyl -5 -naphthal en- I 3 0~ yl-2,4-dioxo-imidazolidin-1-yl} N NN.J il OH -acetyl am ino)-4-m ethyl sulfanyl \-N0 0 -butyric acid methyl ester 3-[2-(1H-imidazol-4-yl)-e Sthy1] -5 -inethyl -5-naphthalen-1I- 4 0~ 0 yl-2,4-dioxo-imidazolidin-1-yl) N-I 1 OH acetylamino)-4-methylsulfanyl 0 0 -butyric acid WO 99/05117 WO 9905117PCT/KR98/00225 14 Table lb
COM.
NO.
Formula Nomenclature 2- 2-[3-(3H-imidazol-4-yl -mn sl ethyl)-5-m ethyl -5 -naphthal en -I -yl-2,4-dioxo-imidazolidin- 0 I~N~ 3-yl ]-acetyl amino)}-4-methyl s ON N C4 ulfanyl-butyric acid methyl ester 2- {2-[3-(3H-imidazol -4-yl-mn -naphthal en 6 N 00 OH -yl-2,4-dioxo-imidazoli din- HN YN-1 I -yl]-acetyl amino) -4-methyl s 0O ulfanyl-butyric acid {3-[3-(4-cyano-benzyl)- N 7 N 0cx hyl-5-naphthalen-1 -yl-2,4-dio N N,)N ocH, xo-imidazolidin- 1-yJ }-acetyla NC N" N mi no)-4-m ethyl sul fanyl-buty ric acid methyl ester 3-[3-(4-cyano-benzyl)- N~ midazol-4-yl)-methyl -met 8 1 N 0hyl-5-naphthalen-1-yI-2,4-dio N N) NH 1- xo-imidazolidin- 1-yl)}-acetyla NC 0 mino)-4-methylsulfanyl-buty ric acid WO 99/05117 WO 9905117PCT/KR98/00225 15 Table lc
COM.
NO.
Formula Nomenclature A 4 2-(2-({3-[3-(3H-imidazol-4-yJ propyl AI -yl-2,4-dioxo-imidazolidin- I -yi }-acetylamino)-3-thiophen-2 -yl-propionic acid 3-[3-(3H-imidazol-4-yl)-propyl en-I -yiI -(2-oxo-2-thiazolidin-3 -yI -ethy Il)-imidazolidin-2,4-dione 1 -dioxo-thiazoildin-3-y N o~ l)-3-(3H-imidazol -4-yI )-propyl N1 0 N~.N
HN
KI0 imidazolidin-2,4-dione 3-[3-(3H-imidazol-4-yl)-propyl -5-methyl- I-({2-[2-(2-methyl s 12 N/ 0~ ulfanyI-ethyl)-thiazolidin-3-yl] y K N -2-oxo-ethyll-5-naphthalen-1- 0 yi-imidazolidin-2,4-dione WO 99/05117 WO 9905117PCT/KR98/00225 16 Table Id
COM.
NO.
Formnula Nomenclature N. ~-O=S NN OH HN
NEI
2 -(2-(3-[3-(3H-imidazol-4-yI)propyl]-5-methyl -1 -yi-2,4-dioxo-imidazolidin- I -yl -acetylamino)-4-methylsulf onyl-butyric acid l 14 0 2,4-dioxo-imidazolidin-1-yl]-a y N NE OH1 cetylamino)}-4-methylsulfanyl- 00 butyric acid N. 2-f2-[3-(2-imidazol-1 -yI-ethyl) N. -5-methyl-5-naphthalen-1-yl-2, 0 4-dioxo-imidazolidin- 1 -yl]-ace rN N ANH OH tyl amino)}-4-methyl sulfanyl -bu N1 0 0 tyric acid 16 I -benzyl-3-(3-imidazol-1 -yl-pr opyl)-5-methyl-5-naphthalen- 1 -yi-imidazolidin-2,4-dione WO 99/05117 WO 99/51 17PCT/kR98/00225 17 Table le
COM.
N.Formula Nomenclature I -(pentafluoro-benzyl)-3 -im 17 F F idazol-1 -yl -propyl)-5 -mnethyl -naphthalen-1I-yl-imidazolidin- O FF 2,4-di one I 1-(3-pyridylmethyl)-3-(3-imida 18 N"1zol- I -yl-propyl)-5-methyl N N phthalen-1 -yl-imidazolidin-2,4- 0 dione 1 -(3-chloro-benzyl)-3-(3-imida 19 zol- 1-yl-propyl)-5-methyl-5-na N phthalen- 1 -yl-imidazolidin-2,4- Ci dione I 1-(3-bromo-benzyl)-3-(3-imida zol- 1 -yl -propyl)-5-methyl NIN phthalen-1I -yl -imidazoli din-2,4-.
Br dione WO 99/05117 WO 9905117PCT/ER98/00225 18 Table If
I
COM.
NO.
Formula Nomenclature It£_ N Br I -(4-bromo-benzyl)-3 -(3-imid azol-1 -yi-propyl)-5-methyl naphthalen-1I-yi-imidazolidin- 2,4-dione 1 -trifluorom ethyl -b enzyl)-3 22 -(3-imidazol- Ni ethyl-5-naphthalen-1-yl-imida
YCF
3 zolidin-2,4-dione 23 CF3 1;(3-trifluoromethoxy-benzyl) I 3-(3-imidazol-1-y-propyl)-- 24 ONNI-N methyl-5-naphthaien-1 -yi-1-(4 24 -phenoxy-benzyl)-imidazolidi Y n-2,4-dione WO 99/05117 WO 9905117PCT/KR98OO225 19 Table Ig CO.Formula Nomenclature
NO.
3-(3-imidazol-1I-yI-propyl)-5- N'~1methyl-5-naphthalen-1-yl-l-(3 N -phenoxy-benzyl)-imidazolidi 0 n-2,4-di one 3-(3-imidazol- I-yl-propyl)- I-( 4-methyl sulfanyl -benzyl 26 N"1Iethyl-5-naphthalen-1-yl-imida zolidin-2,4-dione 0 N 1 3-(3-imidazol-l 27 methyl-I -(4-methylsulfanylme N N thyl-benzyl)-5-naphthalen- I -yl Y -imidazolidin-2,4-dione 3-(3-imidazol-1 28 mnethyl -I -(4-methyl sulfonyl -be N nzyl)-5-naphthalen-1-yl-imida N YN zolidin-2,4-dione WO 99/05117 WO 9905117PCT/KR98/00225 20 Table 1h Formula Nomenclature NO.)(-miao- ylpoy) 5-methyl-5-naphthalen-1I-yI-2, 29 4-dioxo-imidazolidin-1I -ylmeth N y N CN yi ]-2-methyl sulfanyl -benzonitr 0 Hle 5-[3-(3-imidazol- I -yl-propyl)- I5-methyl-5-naphthalen-I-yI-2, \71 4-dioxo-imi dazolidin- I-yl meth Y CN yi]-2-methyl sulfonyl-benzonitr 0 ile I2-[3 -(3-imi dazol- I-yI-propyl)- 31~ N15-methyl -5-naphthalen-lI-yl-2, N 4-di oxo-imidazolidin- 1 -ylmeth CN yl]-benzonitrile 3-[3 -(3-imidazol- I-yl-propyl)- N~~1 I5-methyl-5-naphthalen-1-yl-2, NCNN 4-dioxo-imidazolidin-1I-ylmeth Y a CN yl]-benzonitrile WO 99/05117 WO 9905117PCT[KR98/00225 21 Table li CO .Formula Nomenclature
NO.
4-13-(3-imidazol- 1-yl-propyl) 33CN -5-methyl-5-naphthalen-1-yi- N N 2,4-dioxo-imidazolidin-1-ylm Y ~ethyl] -benzonitri le 1 -(4-aminom ethyl -benzyl)-3( 0 NH2 3-imidazol-1 Ni N thyl-5-naphthalen- I-yl-imidaz Y olidin-2,4-dione N- -(3-imidazol -1-yl -pro 35N"1pyl)-5 -methyl -5 -naphthal en -I N -yl -2,4-dioxo-i m idazoli din- I- 0yl methyl ]-benzyl I}-methanesu I1 Ifonamide I pyl)-5-methyl-5-naphthalen-
I
0N 36 N"1I-yl -2,4-di oxo-i midazoli din-1I- 0 il11 ylmethyl]-benzyi }-methanesu I0 Ifonamide WO 99/05117 WO 9905117PCT/KR98/00225 22 Table lj
COM.
N.Formula Nomenclature I N-f 4-[3-(3-imidazol-1-yl-pro NH pyl)-5-methyl-5-naphthalen- 1 37 ~-yl -2,4-di oxo-i mi dazol idi n- I1y N ylmethyl ]-benzyl ethanesu 0 lfonamide 4 [3 -i midazol -1I-yl -propyl) 0.I -5 -methyl -5 -naphthalen-1I-yl 38 0 2,4-dioxo-imidazolidin- I-ylm yN ethyl]-benzoic acid methyl 0 ester 4-[3-(3-imidazol- 1-yl-propyl) OH -5-methyl-5-naphthalen-1 -yl- NI 2,4-dioxo-imidazolidin-1-ylm ethyl]-benzoic acid 3-(3-imidazol- 1-yl-propyl)- 1- [3 -(morpholine-4-carbonyl)-b -5-naphthal e n-I -yl-imidazolidin-2,4-dione WO 99/05117 WO 9905117PCTJKR98/00225 23 Table 1k
COM.
NO.
Formula Nomenclature 4-[3-(3-imidazol-1-yl-propyl) HN -5-methyl-5-naphthalen-1-yl- 41 0 2,4-dioxo-imidazolidin-l-ylm NYN ethyl ]-N-(2-methoxy-ethy l)-b 0 enzamide 4-[3-(3-imidazol-1-yl-propyl) 42 ~2,4-dioxo-imidazolidin-1 -ylm NYN ethyl] ethoxy-ethyl 0 N-methyl-benzamide 0 4-{4-[3-(3-imidazol-1 -yl-pro N pyl)-5-methyl -5-naphthal en-I1 43 *N _yl-2,4-dioxo-imidazolidin-l- 43- N ylm ethyl enzoyl})-p] perazi n 0 e-1-carboxylic acid benzyl ester 0 3-(3-imidazol- 1-yI-propyl)-l I [3-(thiomorpholine-4-carbon 04 N-s yl)-benzyl] -5 -methyl Y Nhalen- I -yl-imi dazoli din-2,4-d 00 ione WO 99/05117 WO 9905117PCT/KR98/00225 24 Table 11
COM.
NO.
Formula Nomenclature
CN
I -(4-methyl 4-naphthal N/'N 0 n- I -yl)-propyl]-imidazol- Il-yl _N Y N methyl)-benzonitnile
CN
4- 5-[3 -m ethyl -4-methyl I 4-naphthal en- I 46 0 midazolidin-I -yl)-propyl]-im
N
4 N idazol- I -ylmethyl )-benzonitr Y Hle
CN
-ethyl -4-methyl -4- 47 Oj naphthalen-1I-yl-2,5-dioxo-im N0/ idazolidin-1 -yi)-propyl]-imid N Y azol-1 -ylmethyl 1-benzonitfile
CN
5-[3 -(3-propyl-4-methyl-4 I -naphthalen- I 48 0midazolidin-I -yl)-propyll-im N N d~o-1-ylmethyl}-benzonitr Y ile WO 99/05117 WO 9905117PCT/KR98/00225 25 Table Im
COM.
N.Formula Nomenclature
CN
I 4- 5-[3 -(3-butyl-4-methyl-4- 'N Inaphthalen- 49 //--Nidazolidin- 1 -yl)-propyl]-imid N azol- I-ylmethyl} -benzonitrile
CN
3 -[3-(2-methoxy-ethox I ymethyl)-4-methyl-4-naphtha 0len-1-yl-2,5-dioxo-imidazolid N~Nin- I -yl]-propyl }-imidazol- I -y Imethyl )-benzonitril e
CN
(34-1 3-[3 -(4-cyanobenzyl)-3H I 'N -imidazol-4-yl]-propyl} 51 'N ~thy]-5-naphthalen- I-yl-2,4-di N NjJoxo-imidazolidi n- I -yl)-acetic N Y N Ojacid ethyl ester (3-{3-[3-(4-cyanobenzyl)-3H I -yl-2,4-di oxo-imidazolidin- I -yl)-acetic acid WO 99/05117 PTK9/02 PCT/KR98/00225 26 Table In
COM.
NO.Formula Nomenclature
CN
4 [3 -benzyI -4-methyl-4 I -naphthalen-1-yl-2,5-dioxo-i 53 midazolidin-I -yl]-propyl }-im 01--N idazol-1-ylmethyl)-benzonitri -N N Y le
CN
3-[3-(3-cyano-benzyl)- 4-m ethyl -4-naphthalen- I-yl -2 54 NN N ropyl}-imidazol-1-ylmethyl)- Y :a CN benzonitrile
CN
4- 5-[3 -furan-2-yl methyl I 4-methyl-4-naphthalen- 1 -yI- 2 0,5-dioxo-imidazolidin- I-yl)-p 11 N N ropyl-imidazol-1-ylmethyl}-, Y benzonitrile WO 99/05117 WO 9905117PCT/KR98/00225 27- Table CO.Formula Nomenclature
NO.
CN
4-(5-({3-[3-(furan-2-carbonyl) N -4-methyl-4-naphthalen- I -yl- 56 2,5-dioxo-imidazolidin-1-yl]- N1N 0 ropyl)-imidazol-1-ylmethyl) NYN p.
p -benzonitrile CN 3-[3-(4-cyano-benzy I I)-3H-imidazol-4-yl]-propyl) 57 0S 11'-N 0 2,4-di oxo-imidazoli din- Il-yI)- N 10, _N N 24'NH 0 acetylamino] -4-methyl sulfan 0 0 yl-butyric acid methyl ester CN 3-[3-(4-cyano-benzy I N )-3H-imidazol-4-yl]-propyl) 58 0' N 01- 2,4-dioxo-imidazolidin-1I -yl)- N
I
_N YN2JN OH acetylamino]-4-methyl sulfan 0 0* yl-butyric acid
CN
N ethyl -4-naphthal en- 59 N 1-yl-2,S-dioxo-imidazolidin- N YNH thyl]-benzonitrile WO 99/05117 WO 9905117PCT[KR98/00225 28 Table Ip
COM.
NO.
Formula Nomenclature 4.
CN
N N0- N YNI 0 -methyl -4-methyl -4-n aphthalen- I -yl-2, dazolidin- I -ylmethyl)-imidaz ol- I -ylmethyl]-benzonitrile
CN
I4- -ethyl -4-methyl -4-nap 61 Ihthalen- N //-N0-zolidin-1I-ylmethyl)-imidazol N Y -ylmethyl]-benzonitnile
CN
{3-[3-(4-cyano-benzyl)-3H-i 62 1- 5-naphthal en-1I-y I-2,4-di oxo N\ -imidazoli di n- I-yl} -aceti c Y acid ethyl ester
CN
4- {5-[3-(3-cyanobenzyl)-4-m Iethyl -4-naphthal en- I-y 1-2,5 -d 63 /Nioxo-imidazolidin-1-ylmethyl N N N ]-imidazol-1-ylmethyl)-benz CN onitrile WO 99/05117 WO 9905117PCT/KR98/00225 29 Table Iq CO .Formula Nomenclature
NO.
~-~-3-(3-imidazol-1 -yI-propyl)-l 64 NN yi-5-naphthalen-1I-yi-imidazo Y lidin-2,4-dione 0 0 N I 3-(3-imidazol-1I-yi-propyl)-5- N'10 m ethyl-1I-(morphol ine-4-carb N N onyl)-5-naphthalen- 1-yl-imid Yh Y azolidin-2,4-dione -3 -(3-imidazol-1 m methyl -5 -naphthal en-1I-yI -2,4 66 N~]-dioxo-imidazolidine-l1-carbo N N NYH C xylic acid (3-cyano-phenyl)- 0 0 amide N-(4-cyano-tetrahydropyran- 0 4 -(3-imidazol- l-yl-p 67 ropyl)- 5-methyl -5 -naphthal en N N NQH CN -I -yl-2,4-dioxo-imidazolidin- 0~ 1 -yl]-acetamide WO 99/05117 WO 9905117PCT/KR98/00225 30 Table Ir CO .Formula I Nomenclature
NO.
Br 3-{3-[3-(4-bromo-benzyl)-3 68 H-imidazol-4-yl]-propyl 68N 0-7 methyl-5-naphthalen-1I -yl-imi N YNHl dazolidin-2,4-dione Br 3-t{3-[3-(4-bromo-benzyl)-3 69 ~H-imidazol-4-yi]-propyl} 69 N 04 -dimethyl-5-naphthalen-I -yl N Y N ,imidazoliclin-2,4-dione Br0 Br {3-[3-(4-bromo-benzyl)-3 N H-imidazol-4-yl]-propyl ~methyl-5-naphthalen- I-yl-2,4 N J 0 -dioxo-imidazolidin-l -yI)acet Y ic acid ethyl ester I 3-[3-(3-imidazol-1-yI-propyl) 71 N'l1 -5-methyl-5-phenyl-2,4-diox N CN o-imidazolidin-1-ylmethyl]-b ,NN Y N a CNenzonitrile WO 99/05117 WO 9905117PCTIMR8/00225 31 Table Is
COM.
NO.
Formula Nomenclature
CN
4-[5-(3-naphthalen- 72 dioxo-imidazolidin-1 -ylmeth N yi)-imiaazol- 1 -ylmethyl]-be
NN
y N nzonitrile C1 I 3-[3 -(4-chl oro-benzyl)-3H-i 73 0 midazol-4-ylmethyl]- 1 -napht
N
N dione 00 4-[5-(3-naphthalen- I N dioxo-imidazolidin-1 -ylmeth 74 Y ,yi)-imidazol-1 -ylmethyl]-pip 11-N 0eridine-1-carboxylic acid
N
N N N/ benzyl ester C N -naphthal en-1I -ylImeth 0 yl-2,5-dioxo-imidazoli din-1I N 1- ylmethyl)-imidazol- I-ylmeth NN I yi]-benzonitrile WO 99/05117 WO 9905117PCT/KR98/00225 32 Table It CO.Formula I Nomenclature
NO.
OY 4-[5-(3-naphthalen- I -ylmeth N yl-2,5-dioxo-imidazoli din- 1 76 ylmethyl)-imidazol-1I -ylmeth Y ,N yl-pi peridine- I -carboxyli c N NN acid benzyl ester 0N CN {1 -(4-cyano-benzyl)-3H-i midazol-4-ylmethyl]-3-napht halen- I-ylmethyl N1- midazolidin-4-yl) -acetic
N
NYN, acid ethyl ester
CN
{I -[3-(4-cyano-benzyl)-3H-i 0 O midazol-4-ylmethyl]-3-napht 78 0 halen-1I-ylmethyl N. N N midazolidin-4y}aei N' acid
CN
{11 -(4-cyano-benzyl)-3H-i N 0 midazol-4-ylmethyl]-3-napht 79N halen- N N1-N midazolidin-(4S)-yl) -acetic Y acid methyl ester WO 99/05117 WO 9905117PCT/KR98/00225 33 Table lu
COM.
NO.
Formula Nomenclature CN 0 4-f{ 5-[4-(2-morpholin-4-yl-2 0 -oxo-ethyl)-3 -naphthal en- I-y 11-N 0lmethyl-2,5-dioxo-imidazoli N N N_,I din-]1-ylmethyl]-imidazol-l- Y ylmethyll-benzonitrile CN 0 1 No4- {(5S)-[4-(2-morpholin-4-y N_ 1-2-oxo-ethyl)-3-naphthalen- 810' 1 -ylm ethyl -2,5 -di oxo-imi daz olidin- 1-ylmethyl]-imidazol- I I -ylmethyl }-benzonitrile CN 2- 1-[3 -(4-cyano-benzyl)-3 9 H H-imidazol-4-ylmethyl]-3 -na 82 00phthaien- I N N N,N-dimethylamino)-ethyl)- 0 acetamide Br 1-[3-(4-bromo-benzyl)-3 N H-imidazol-4-ylmethyl]-3-na 83 0 0phthalen- 1 -ylmethyl N.x-mdzldn4y)--2 NN \-mdoiin4y)--2 INY methoxy-ethyl)-N-methyl-ac 0 etamide WO 99/05117 WO 9905117PCT/KR98/00225 34 Table Iv
COM.I
N.Formula Nomenclature CN N [2-(4-methyl-pipe I No razin- I-yI)-2-oxo-ethyl]-3-na 84 0 0phthalen- 01' o-imidazolidin- I -ylmethyl
N\_
N YN _j mi dazol-1I-ylmethyl)-benzoni 0 trile CN 0 (2S)-(2-{1I-[3-(4-cyano-benz 0 M yl)-3H-i mi dazol -4-ylm ethyl 0 0 _3-naphthalen-1I-ylmethyl-2,5dioxo-imidazolidin-4-yi )-ace NYN tylamino)-4-methylsulfanyl-b 0 utyric acid methyl ester CN 0 I-[3-(4-cyano-benz NH OH yl)-3 H-i mi dazol -4-yl methyl] 86 003-naphthalen- I -ylmethyl-2, 1N dioxo-imidazolidin-4-yl} -ace NYN tylamino)-4-methylsulfanyl-b 0 utyric acid 0 3-(3-imidazol-I -yl-propyl)- I- 87 NN-, N YN naphthalen-I -yl-imidazolidin 0 I6 -2,4-dione WO 99/05117 PCT/KR98/00225 35 It is another object of the present invention to provide a process for preparing the hydantoin derivative of formula as defined above.
According to the present invention, the hydantoin derivative of formula can be prepared by a process characterized in that 1) a compound represented by the following formula (II): [Formula II] o R, HN N-R 4 o wherein R 1
R
2 and R4 are defined as previously described, is reacted under Mitsunobu reaction condition with an alcohol derivative represented by the following formula (III): [Formula III]
R
3
-OH
wherein R3 is defined as previously described, or 2) a compound represented by the following formula (IIa): [Formula IIa] o R, HN NH WO 99/05117 PCT/KR98/00225 36 wherein Ri and R 2 are defined as previously described, is reacted with the alcohol derivative of formula (III) under Mitsunobu reaction condition to produce a compound represented by the following formula (Ia): [Formula la] o R, -R2 R3 -N -NH
O
wherein Ri, R 2 and R 3 are defined as previously described, then substituent R 4 is introduced into the resulting compound of formula (Ia) to produce a compound represented by the following formula (Ib): [Formula Ib] HLR2
R
3 ,N N -R 0 wherein Ri, R2 and R3 are defined as previously described and R4' is the same as R 4 except that R4 is not hydrogen.
While, the starting compounds used in the above reaction may be prepared according to the processes depicted in the following Schemes 1 to 9. First, the compound of formula (IIa) can be synthesized by condensing a ketone compound with potassium cyanide and ammonium carbonate as represented in the following Reaction Scheme 1: WO 99/05117 PCT/KR98/00225 37 [Reaction Scheme 1] 0 O R
(NIH)
2
CO
3 KCN HN NH R2 (2a) As represented in the following Reaction Scheme 2, the compound of formula (II) can be prepared from ethyl bromoacetate by alkylation of amine compound and cyclization: [Reaction Scheme 2] 0 0 Br 0. H 2
N-R
4 I r 0 HNR KOCN HN NR4 Further, the compound of formula (II) may be obtained by processes represented in the following Reaction Schemes 3 and 4.
Specifically, a racemate can be obtained through the alkylation of an amine compound using fumarate and then cyclization as Reaction Scheme 3, and a stereospecific isomer can be obtained through the reductive amination of an aspartic acid having ester protecting group with an aldehyde compound and then cyclization as Reaction Scheme 4: WO 99/05117 PCT/KR98/00225 38 [Reaction Scheme 3] 'O 0-"-1O
H
2
N-R
4 0 0 0 HNR 4 AcOH
KOCN
0 0
ONR
[Reaction Scheme 4] 0 0
NH
2 AcOH
KOCN
OHC-R4 0 0 HN 0 0 HN N-R The alcohol compound of formula (III) may be prepared by processes described in the following Reaction Schemes 5 to 9. That is, the compound 3 can be synthesized by forming imidazole moiety using dihydroxy acetone as Reaction Schemes 5 and 6, or by alkylating the existing imidazole methanol compound as Reaction Scheme 7. Also, the compound of formula (III) may be prepared by processes described in the following Reaction Schemes 8 and 9.
WO 99/05117 PTK9/02 PCT/KR98/00225 39 [Reaction Scheme
HNZX--NH
2 Benzaldehyde_ HC
N-
1. CbzCI 2. KHS0 4 CbzlqN
N
2
KSCN
0 HO,, OH HN0 3 [Reaction Scheme 6]
KSCN
0 HO.JkOH HN0 3 [Reaction Scheme 7] N1
OH
FIN He] it-Cl ND OH
N
Trt/ N D OAc
(ACO)
2 0
N
Trt/ TF A 4-Bromomethyl benzonitrile Br W W99/05117 PTK9/02 PCT/KR98/00225 40 [Reaction Scheme 8]
O
0 N- N N [Reaction Scheme 9]
O
Br O N LiAIH 4
OH
N 0 In the above Reaction Schemes, AcOH represents acetic acid, Cbz-Cl represents benzyloxycarbonyl chloride, Trt-Cl represents chlorotriphenylmethane and TFA represents trifluoroacetic acid. The process for preparing the compound of formula particularly the synthetic methods as described above will be more specifically explained by the following Preparations and Examples.
As the coupling agent used in the above amidation reaction for preparing the compound of formula a mixture of carbodiimides such as dicyclohexylcarbodiimide(DCC), 1-ethyl-3-(3-dimethylaminopropyl)carbo diimide(EDC), 1,1'-dicarbonyldiimidazole(CDI), etc., and 1-hydroxybenzotrizole can be mentioned.
Reaction conditions including the amount of reactants, temperature, reaction time, etc. can be easily determined by the person having ordinary skill in the art depending on the reactant used.
Also, the free comopund of formula produced in the WO 99/05117 PCT/KR98/00225 41 aforementioned reaction may be easily converted into a salt form thereof according to the conventionally known methods in this art.
After the reaction is completed, the resulting product may be further separated and purified by usual work-up processes, such as for example, chromatography, recrystallization, etc.
The compound of formula shows an inhibitory activity against farnesyl transferase, and thus can be effectively used as an anti-cancer agent.
Therefore, the present invention also provides an anti-cancer agent comprising the novel compound of formula as defined above, or a pharmaceutically acceptable salt thereof as an active ingredient together with a pharmaceutically acceptable carrier.
When the active compound according to the present invention is used for clinical purpose, it is preferably administered in an amount ranging from 10 mg to 4 0 mg per kg of body weight a day. The total daily dosage may be administered in one time or over several times.
However, the specific administration dosage for the patient can be varied with the specific compound used, body weight of the subject patient, sex, hygienic condition, diet, time or method of administration, excretion rate, mixing ratio of the agent, severity of the disease to be treated, etc.
The compound of the present invention may be administered in the form of injections or oral preparations. Injections, for example, sterilized aqueous or oily suspension for injection, can be prepared according to the known procedure using suitable dispersing agent, wetting agent, or suspending agent. Solvents which can be used for preparing WO 99/05117 PCT/KR98/00225 42 injections include water, Ringer's fluid and NaCI solution, and also sterilized fixing oil may be conveniently used as the solvent or suspending media. Any non-stimulative fixing oil including mono-, di-glyceride may be used for this purpose. Fatty acid such as oleic acid may also be used for injections.
As the solid preparation for oral administration, capsules, tablets, pills, powders and granules, etc., preferably capsules and tablets can be mentioned. It is also desirable for tablets and pills to be formulated into enteric-coated preparation. The solid preparations may be prepared by mixing the active compound of formula according to the present invention with at least one carrier selected from a group consisting of inactive diluents such as sucrose, lactose, starch, etc., lubricants such as magnesium stearate, disintegrating agent and binding agent.
The present invention will be more specifically explained in the following examples. However, it should be understood that the following examples are intended to illustrate the present invention but not in any manner to limit the scope of the present invention. Processes for preparing the starting substances used for obtaining the compound of formula will be explained in the following Preparations.
Preparation 1 Synthesis of 5-methyl-5-naphthalen-1-yl-imidazolidin-2,4-dione 30g(0.18 mol) of l'-acetonaphthone and 23g(0.35 mol) of potassium cyanide[KCN] were dissolved in 9 00 mg of methanol. Then, 169g(1.8 mol) of ammonium carbonate[(NH 4 )2CO 3 in 9 0 0nPi, of distilled water were added thereto and the resulting solution was stirred for 12 hours at 70 C. The reaction solution was distilled under reduced WO 99/05117 PCT/KR98/00225 43 pressure to remove methanol and the residue was extracted with ethyl acetate(500 m x The extract was distilled under reduced pressure to remove ethyl acetate and 38.2g(Yield: 90%) of title compound was obtained.
'H NMR(CDCl 3 a (ppm) 2.15(3H, 6.35(1H, 7.44(1H, t), 7.53(2H, 7.70(1H, 7.89(1H, 7.93(1H, 7.99(1H, 8.52(1H, br) FAB Mass(M+H) 241 Preparation 2 Synthesis of 1-naphthalen-1-yl-imidazolidin-2,4-dione 2-1) Synthesis of (naphthalen-1-yl-amino)-acetic acid ethyl ester 19.3g(139 mmol) of potassium carbonate was added to 20 0 mg of dimethylformamide, and then the solution was heated to dissolve potassium carbonate. After cooling to room temperature, 8 mj( 7 0 mmol) of ethyl bromoacetate and 10g(70 mmol) of I-naphthylamine were added to the solution, which was then stirred for 48 hours. DMF was removed under reduced pressure and ethyl actate was added to the residue. The ethyl acetate layer was washed with water 4 times and saturated sodium chloride solution. Ethyl acetate was removed under reduced pressure, and then column chromatography was performed using a mixed solution(9:1) of hexane and ethyl acetate as an eluent to obtain 12g of the title compound(Yield 75%, MW 229).
'H NMR(CDC1 3 8 (ppm) 1.33(3H, 4.07(2H, 4.30(2H, q), 6.24(1H, 7.30(1H, 7.34(1H, 7.47(2H, 7.80(1H, m), 7.95(1H, m) FAB 230 WO 99/05117 PCT/KR98/00225 44 2-2) Synthesis of 1-naphthalen-1-yl-imidazolidin-2,4-dione 8.68g(37.9 mmol) of the compound prepared in Preparation 2-1) and 6.34g(75.8 mmol) of potassium isocyanate were added to 100l of acetic acid and the solution was stirred for 24 hours at 110 C. Acetic acid was removed under reduced pressure and then ethyl acetate was added to the residue. The resulting solution was washed with water 3 times, IN HCI solution, saturated sodium bicarbonate solution, and saturated sodium chloride solution, respectively. The solution was recrystallized from ethyl acetate to obtain 6.8g of the title compound(Yield 80%, MW 226).
'H NMR(CD 3 0D) a (ppm) 4.49(2H, 7.52-7.61(4H, m), 7.89-7.98(3H, m) FAB 227 Preparation 3 Synthesis of 1-(naphthalen-1-ylmethyl)-2,4-dioxo-imidazolidin-5-yl]acetic acid ethyl ester 3-1) Synthesis of 2-[(naphthalen-1-ylmethyl)-amino]succinic acid diethyl ester 3.12,m(19.0 mmol) of diethyl fumarate and 3.0g(19 mmol) of 1-aminomethyl naphthalene were added to acetonitrile, and then the solution was refluxed for 12 hours. Acetonitrile was removed under reduced pressure and column chromatography was performed using a mixed solution of hexane and ethyl acetate(3:1) as an eluent to obtain 4.57g of the title compound(Yield 73%, MW 329).
1H NMR (CDC1 3 8 (ppm) 1.19(3H, 1.30(3H, 2.18(1H, br), 2.70 (2H, 2dd), 3.79(1H, dd), 4.03-4.13(2H, 4.15(1H, 4.23(2H, WO 99/05117 WO 9905117PCT/KR98/00225 45 4.35 (1H, 7.41(1H, 7.45-7.55(3H, in), 7.77(1H, 7.85(1H, d), 8.20(1H, d) FAB 330 3-2) Synthesis of [1 -(naplithalen- 1 -ylmethyl)-2,4-dioxo-imidazolidin-5 -yl] ace tic acid ethyl ester 4.57g(13.9 minol) of the compound prepared in Preparation 3-1) and 3.38g(4 1.7 mmol) of potassium isocyanate were added to 1 5 0 fl~ of acetic acid and the solution was stirred for 24 hours at l1O"C. Acetic acid was removed under reduced pressure and ethyl acetate was added to the residue. The resulting solution was washed with water 3 times, IN HCl solution, saturated sodium bicarbonate solution and saturated sodium chloride solution, respectively. Ethyl acetate was removed under reduced pressure and then column chromatography was performed using a mixed solution of hexane and ethyl acetate(l: 1) as an eluent to obtain 3.85g of the title compound(Yield 85%, MW 326).
1 NMR (CDCl 3 a (ppm) 1.08(3H, 2.70(2H, 2dd), 3.80(lH, in), 3.90 in), 4.80(1H, 5.30(lH, 7.38-7.46(2H, in), 7.51(lH, 7.57(lH, in), 7.83(1H, in), 7.87(lH, 8.l0(1H, 9.27(lH, s) FAB 327 Preparation 4 Synthesis of It1-(n aphthalen-1 -ylm ethyl)-2,4-d io xo-imni dazo lid in-(5S)-yl a c etic acid methyl ester 4-1) Synthesis of (2S)-[(naphthalen- 1-ylmethyl)-amino] succinic acid diethyl ester 2.22g(1 1.2 minol) of (S)-diinethyl aspartate hydrochloride and 1.6 rnf(l1.2 inmol) of l-naphthyl aldehyde were added to 50H~p of WO 99/05117 PCT/KR98/00225 46 dimethylformamide, and then the solution was stirred for 1 hour.
5.0g(22.4 mmol) of sodium triacetoxy borohydride was added to the solution and the resulting solution was stirred for 4 hours. Then, DMF was removed in vacuo and then ethyl acetate was added thereto. The solution was washed with water and saturated sodium chloride solution.
Ethyl acetate was removed under reduced pressure and column chromatography was performed on the residue using a mixed solution of hexane and ethylacetate(3:1) as an eluent to obtain 3.00g of the title compound(Yield 89%, MW 301).
1H NMR (CDCl 3 a(ppm) 2.23(1H, br), 2.74(2H, 2dd), 3.60(3H, 3.77 (3H, 3.81(1H, dd), 4.15(1H, 4.34(1H, 7.41(lH, t), 7.44-7.55(3H, 7.77(1H, 7.84(1H, 8.18(1H, d) FAB 302 4-2) Synthesis of [1-(naphthalen-1-ylmethyl)-2,4-dioxo-imidazolidin-(5S)-yl] acetic acid methyl ester 3.00g(9.96 mmol) of the compound prepared in Preparation 4-1) and 2.2g(26 mmol) of potassium isocyanate were added to 50nm of acetic acid and then the solution was stirred for 30 minutes at 110°c.
Acetic acid was removed under reduced pressure and ethyl acetate was added to the residue. The resulting solution was washed with water 3 times, IN HCI solution, saturated sodium bicarbonate solution and saturated sodium hydroxide solution, respectively. Ethyl acetate was removed under reduced pressure to obtain 2.87g of the title compound(Yield 92%, MW 312).
'H NMR (CD 3 0D+CDCl 3 a (ppm) 2.45(2H, 2dd), 3.09(3H, s), 3.75(1H, 4.79(2H, dd), 7.20(1H, 7.27-7.37(2H, 7.63(1H, d), 7.66(1H, 7.90 (1H, d) WO 99/05117 PCT/KR98/00225 47 FAB 313 Preparation Synthesis of 4-(5-hydroxymethyl-imidazol-1-ylmethyl)-piperidine-l-carbo xylic acid benzyl ester 5-1) Synthesis of 4-aminomethyl-piperidine-l-carboxylic acid benzyl ester 22.2g(0.2 mol) of 4-aminomethyl piperidine was dissolved in 250 n, of toluene and 21.2g(0.2 mol) of benzaldehyde was added thereto.
The reaction mixture was heated to reflux for 3 hours with Dean-stack and then cooled down to 0°C. 34.2g(0.2 mol) of benzyl chloroformate was added dropwise while stirring. The reactants were stirred for 3 hours and 2 20 mg of IN KHSO 4 was added at room temperature. The reaction solution was extracted with 200ljs of diethylether 3 times and the aqueous layer was basified with sodium hydroxide. After the aqueous solution was treated with saturated sodium chloride solution, it was extracted with 1 00mg of dichloromethane 3 times, and the organic layer was dried over magnesium sulfate. Removal of dichloromethane under reduced pressure provided 38g of the title compound(Yield 91%, MW 248).
'H NMR(CDCI 3 8(ppm) 1.11(2H, 1.49(3H, 1.70(2H, d), 2.57(2H, 2.78(2H, 4.20(2H, 5.12(2H, 7.34-7.35(5H, m) FAB 249 5-2) Synthesis of 4-(5-hydroxymethyl-2-mercapto-imidazol-1-ylmethyl)-pipe ridine-1-carboxylic acid benzyl ester 24.8g(0.1 mol) of the compound prepared in Preparation 5-1) was dissolved in 5 0 m of n-butanol with 6 .0g(0.1 mol) of acetic acid. Above solution was added to 50 mg of n-butanol solution in which 12.6g(0.13 WO 99/05117 PCT/KR98/00225 48 mol) of potassium thiocyanate, 15.2g(0.1 mol) of 1,3-dihydroxyacetone dimer and 10.0g(0.17 mol) of acetic acid were dissolved, and then the resulting solution was stirred for 48 hours. After stirring, the solvent was removed under the reduced pressure and 2 00me of ethyl acetate was added thereto. The resulting solution was washed with 100lm. of water 3 times and the organic layer was dried over magnesium sulfate. The solvent was removed under reduced pressure to obtain 27g of the title compound(Yield 75%, MW 361).
'H NMR(CDCl 3 a (ppm) 1.22(2H, 1.57(2H, 2.30(1H, s), 2.72(2H, 3.96(2H, 4.15(2H, 4.46(2H, 5.10(2H, 6.62(1H, 7.26-7.37(5H, m) FAB 362 5-3) Synthesis of 4-(5-hydroxymethyl-imidazol-1-ylmethyl)-piperidine- 1-car boxylic acid benzyl ester 18.05g(50 mmol) of the compound prepared in Preparation 5-2) was added to a mixed solution of 100 gm of 10% nitric acid solution and of ethyl acetate at 0'C. It was stirred for 3 hours at room temperature. The reaction solution was basified with 4N aqueous sodium hydroxide solution and then extracted with 1 0 0 mg of ethyl acetate twice.
The extracted organic solution was dried over magnesium sulfate. The solvent was removed under reduced pressure to give 12.3g of the title compound(Yield 75%, MW 329).
1H NMR(CDCl 3 3 (ppm) 1.16(2H, 1.56(2H, 1.98(1H, s), 2.70(2H, 3.88(2H, 4.18(2H, 4.49(1H, 4.56(3H, 5.10(2H, 6.82 (1H, 7.27-7.40(5H, m) FAB 330 WO 99/05117 PCT/KR98/00225 49 Preparation 6 Synthesis of 1-(4-bromobenzyl)-5-hydroxymethyl-imidazole 8.9g(40 mmol) of 4-bromobenzylamine hydrochloride and 4njt of acetic acid were dissolved in 85 mg of n-butanol. 5.19g(50 mmol) of potassium thiocyanate and 3.21g(20 mmol) of 1.3-dihydroxyacetone dimer were added to the solution. The resulting solution was stirred for 4 days and then filtered under reduced pressure to separate the precipitated solid, which was then washed with water and diethylether. The solid thus obtained was added to 10% nitric acid solution, and then the mixture was stirred for 3 hours, filtered under reduced pressure to remove the insoluble impurities. Then, the solution was basified with 4N sodium hydroxide solution to precipitate a solid product. This solid product was washed with water several times and dried under vacuum to give 6.7g of the title compound(Yield 60%, MW 266).
'H NMR(CDC1 3 &(ppm) 4.45(2H, 5.20(2H, 6.94(1H, s), 7.03(2H, 7.18(4H, m) FAB Mass 267 Preparation 7 Synthesis of 4-(5-hydroxymethyl-imidazol-1-ylmethyl)-benzonitrile 7-1) Synthesis of 1-trityl-4-hydroxymethyl-imidazole 7.98g(59.2 mmol) of hydroxymethyl imidazole hydrochloride was dissolved in a solvent mixture of 6 0m{i of dimethylformamide and of triethylamine. 2 00n of dimethylformamide solution containing 18.7g (67 mmol) of triphenylmethyl chloride was added slowly thereto. After 2 hours, l000Me of ice water was added thereto to obtain a solid. This solid was recrystallized from dioxane to give 17.6g of the title WO 99/05117 PCT/KR98/00225 50 compound(Yield 87%, MW 340).
mp 227-229 °C.
7-2) Synthesis of 1-trityl-4-hydroxymethyl-imidazole acetate 10.0g(29.4 mmol) of the compound prepared in Preparation 7-1) was added to 2 0 0 mn of pyridine and then, 3.30g(32.4 mmol) of acetic anhydride was added. After stirring for 24 hous at room temperature pyridine was removed under reduced pressure. The residue was dissolved in 4 00mi of ethylacetate, and then washed with 2 0 0 mg of saturated sodium chloride solution. After removal of ethyl acetate under reduced pressure, chromatography was performed on the residue using dichloromethane/ methanol(95:5) as an eluent to obtain 10.44g of the title compound(Yield 93%, MW 382).
'H NMR(CDCl 3 a (ppm) 2.01(3H, 4.95(2H, 6.88(1H, s), 7.08(5H, 7.27(10H, 7.45(1H, s) FAB 383 7-3) Synthesis of 1-trityl-3-(4-cyanobenzyl)-imidazol-4-ylmethyl acetate bromide 10.0g(26.2 mmol) of the compound prepared in Preparation 7-2) was dissolved in 4 0 rn of dichloromethane and 5.64g(28.8 nmmol) of 4-cyanobenzyl bromide was added thereto. The resulting solution was stirred for 60 hours at room temperature and dichloromethane was removed under reduced pressure. Column chromatography was performed with the residue using dichloromethane/methanol(95:5) as an eluent to obtain 10.62g of the title compound(Yield 70%, MW 578).
'H NMR(CDCl 3
/CD
3 0D) (ppm) 1.95(3H, 4.95(2H, s), WO 99/05117 PCT/KR98/00225 51 5.45(2H, 7.11-7.40(18H, 7.65(2H, 8.21(1H, s) FAB 579 7-4) Synthesis of 1-(4-cyanobenzyl)-imidazol-5-ylmethyl acetate 9.10g(15.7 mmol) of the compound prepared in Preparation 7-3) was dissolved in 500 m, of dichloromethane and 6.06mn(78.7 mmol) of trifluoroacetic acid and 1 2 5 m 7 8 7 mmol) of triethylsilane were added slowly thereto at 0°C. The resulting solution was stirred for 1 hour at room temperature. After removal of dichloromethane under reduced pressure, pH was adjusted to pH 10 using saturated potassium carbonate solution. This solution was extracted with 3 0 0 fm of ethyl acetate and ethyl acetate was removed under reduced pressure. Column chromatography was performed with the residue using ethyl acetate as an eluent to obtain 3.60g of the title compound(Yield 90%, MW 255).
'H NMR(CDCl 3 a (ppm) 1.90(3H, 4.97(2H, 5.25(2H, s), 7.14(2H, 7.21(1H, 7.67(1H, 7.75(2H, d) FAB 256 Synthesis of 4-(5-hydroxymethyl-imidazol-1-ylmethyl)-benzonitrile 3.36g(13.2 mmol) of the compound prepared in Preparation 7-4) was dissolved in 1 6 0 mi of methanol and 3.60g(26.3 mmol) of K 2 CO3 was added thereto. After stirring for 20 minutes at room temperature, methanol was removed under reduced pressure and product was extracted with 2 5 0 mg of ethyl acetate. Column chromatography was performed using dichloromethane/methanol(95:5) as an eluent to obtain 2.55g of the title compound(Yield 91%, MW 213).
'H NMR (CDC1 3
/CD
3 0D) 8 (ppm) 4.28(2H, 5.18(2H, s), 6.84(1H, 7.12(2H, 7.42(1H, 7.55(2H, d) WO 99/05117 PCT/KR98/00225 52 FAB 213 Preparation 8 Synthesis of 3-imidazol-1-yl-propanol 8-1) Synthesis of methyl 3-imidazol- I -yl-propionate 5.0g(73.4 mmol) of imidazole and 12.6g(148.6 mmol) of methyl acrylate were dissolved in 10 0 mi of acetonitrile, and then refluxed for 8 hours. Acetonitrile and the excess methyl acrylate was removed under reduced pressure. Then, 2 00 mg of ethyl acetate was added to the residue and the solution thus obtained was washed with saturated sodium chloride solution. Removal of ethyl acetate under reduced pressure provided 11.lg(Yield: 90%) of the title compound.
'H NMR(CDCl 3 3 (ppm) 2.75(2H, 3.46(3H, 4.24(2H, t), 6.89(1H, 7.00(1H, 7.46(1H, s) FAB Mass(M+H) 169 8-2) Synthesis of 3-imidazol-1-yl-propanol To the 1.1g(6.6 mmol) of the compound prepared in Preparation 8-1) in 50m of tetrahydrofuran was added 0.26g(6.6 mmol) of lithium aluminum hydride[LiAlHI] and then the resulting mixture was refluxed for one hour. Then, 2 0 mg of IN sodium hydroxide solution was added to the reaction mixture which was then extracted with ethyl acetate.
Removal of the organic solvent under reduced pressure provided 0.77g(Yield: 93%) of the title compound was obtained.
'H NMR(CDCl 3 a (ppm) 1.67(2H, 3.26(2H, 3.78(2H, t), 6.60(1H, 6.75(1H, 7.14(1H, s) FAB Mass(M+H) 127 WO 99/05117 PCT/KR98/00225 53 Preparation 9 Synthesis of 2-imidazol-1-yl-ethanol 9-1) Synthesis of 2-imidazol-1-yl-acetic acid ethyl ester 5.0g(73.4 mmol) of imidazole and 3 3 6me(29.4 mmol) of ethyl bromoacetate were dissolved in 5 0 m of dimethylformamide and stirred for 4 hours. Dimethylformamide was removed in vacuo. Then, 100 np of ethyl acetate was added to the residue and it was washed with saturated sodium chloride solution. Removal of the organic solvent under reduced pressure provided 0.77g(Yield: 17%) of the title compound.
IH NMR(CDCl 3 8 (ppm) 1.29(3H, 4.25(2H, 4.70(2H, s), 6.95(1H, 7.10(1H, 7.49(1H, s) FAB Mass(M+H) 155 9-2) Synthesis of 2-imidazol-1-yl-ethanol To the 2 0 Mt of tetrahydrofuran solution of 0.77g(5.0 mmol) of the compound prepared in Preparation 9-1) was added 0.2g(5.0 mmol) of lithium aluminum hydride and then the resulting mixture was refluxed for one hour. Then, 10 g of IN sodium hydroxide solution was added to the reaction mixture, and it was extracted with ethyl acetate. The organic solvent was removed under reduced pressure and the residue was subjected to chromatography using a solvent mixture of methanol-methylene chloride(5:95) as the eluent to obtain 0.51g(Yield: 91%) of the title compound.
'H NMR(CDCl 3 a (ppm) 3.78(2H, 3.98(2H, 6.85(1H, s), 6.94(1H, 7.36(1H, s) WO 99/05117 WO 9905117PCT/KR98/00225 54 FAB Mass(M+H) :113 Example 1 Synthesis of idazol-4-yl)-propyl]-5-methyl-5-naphthalen -1 -yI-2,4-dioxo-im idazolidin-1-yl}-acetylam ino)-4-methylsulfanyl-bu tyric acid methyl ester(Compound 1) 1-1) Synthesis of 3- [3 -(1-triphenylmethyl-imnidazol-4-yl)-propyl]-5 -methyl 1-yl-imidazolidin-2,4-dione 0. 60g(2 .51 minol) of 5-methyl-S -naphthalen- 1-yl-imidazolidmn-2,4dione prepared in Preparation 1, 1.02g(2.76 mmol) of 3)-(l-triphenyl methyl-imidazol-4-yl)-propanol and 0.87g(3 .3 mmol) of triphenyiphosphine (Ph 3 P) were dissolved in 50 mg of tetrahydrofuran. O.52,, (3.3 mmol) of diethylazodicarboxylate [DEAD] was added thereto and the resulting solution was stirred for 24 hours. Tetrahydrofuran was removed under reduced pressure and the residue was subjected to chromatography using ethyl acetate the eluent to obtain 1. 17g(Yield: 80%) of the title compound.
IH NMR(CDCl 3 3 (ppm) 2.04(5H, in), 2.60(2H, 3).67(2H, t), 6.59(1H, 7.05(IH, 7.15(6H, in), 7.32(9H, in), 7.37(1H, 7.44(2H, 7.63(1H, 7.79(1H, 7.86(1H, 7.91(1H, d) FAB Mass(M+H) :591 1-2) Synthesis of 2- {3 1-triphenylmethyl-imidazol-4-yl)-propyl]-5-methyI 1-yl-2,4-dioxo-imidazolidn- 1 -yl }-acetic acid ethyl ester 0.082g(0. 14 mmol) of 3- [3 -(1-triphenytmethyl-iniidazol-4-yl)-propyl] -methyl-5-naphthalen- 1-yl-imidazolidin-2,4-'dione prepared in Example 1-1) and 0.0 23 mg(O.
2 1 minol) of ethyl bromoacetate were dissolved i HIR, of dimethylformamide. 0.017g(0.21 minol) of sodium hydride [NaH] WO 99/05117 PCT/KR98/00225 55 was added thereto and the resulting solution was stirred for one hour.
Dimethylformamide was removed under reduced pressure and the residue was dissolved in ethyl acetate and then washed with saturated sodium chloride solution. Removal of ethyl acetate under reduced pressure provided 0.092g(Yield: 99%) of title compound.
IH NMR(CDC1 3 8(ppm) 1.10(3H, 2.02(3H, 2.15(2H, m), 2.70(2H, 3.80(2H, 4.02(2H, 4.10(2H, 6.60(1H, 7.13(6H, 7.33(11H, 7.46(3H, 7.69(1H, 7.89(2H, m) FAB Mass(M+H) 677 1-3) Synthesis of 2-(2-{3-[3-(1-triphenylmethyl-imidazol-4-yl)-propyl]-5- 1-yl-2,4-dioxo-imidazolidin- l-yl }-acetylamino)-4-methyl sulfanyl-butyric acid methyl ester 0.092g(0.14 mmol) of 2-{3-[3-(1-triphenylmethyl-imidazol-4-yl)- -yl-2,4-dioxo-imidazolidin- -yl}-acetic acid ethyl ester prepared in Example 1-2) was dissolved in 4mC of a solvent mixture of tetrahydrofuran- distilled water(3:1). 0.0058g(0.14 mmol) of lithium hydroxide[LiOH] was added thereto and the resulting solution was stirred for one hour. The solvents were removed under reduced pressure and the residue was thoroughly dried under vacuum. The residue thus produced was dissolved in 5 me of dimethylformamide.
Then, 0.041g (0.21 mmol) of methionine methyl ester, 0.037g(0.28 mmol) of N-hydroxy benzotriazole and 0.04g(0.28 mmol) of 3-ethyl-(dimethyl amino)-propylcarbodiimide hydrochloride were added to the resulting solution and stirred for 12 hours at room temperature.
After removal of dimethylformamide under reduced pressure, 30ne of ethyl acetate was added. The resulting solution was washed twice with 1Oag of saturated potassium carbonate solution and 10ra of saturated sodium chloride solution, sequentially. Then, chromatography using a WO 99/05117 WO 9905117PCT/KR98/00225 56 solvent mixture of ethyl acetate-hexane(: as the eluent was carried out to obtain 0. 1 lg(0.13 minol, Yield: 95%) of the title compound.
'H NMR(CDCJ 3 3 (ppm) 1.84(2H, in), 1.98(6H, in), 2.14(2H, in), 2.40(2H, 2.71(2H, 3.38(1H, dd), 3.62(3H, 3.80(2H, in), 4.46(IH, in), 6.64(1H, 6.75(1H, dd), 7.14(6H, in), 7.24-7.53(13H, in), 7.72(1H, 7.89(2H, m) FAB Mass(M+H) 794 1-4) Synthesis of H-imidazol-4-yl)-propyl]-5 -methyl-5 -naphthalen-I -yl-2,4-dioxo-iinidazolidin- 1-yl }-acetylamino)-4-methylsulfanyl-butyn~c acid methyl ester 0.1 lg(O. 13 inmol) of -triphenylmethyl-iinidazol-4-yl)propyl]-5-methyl-5-naphthalen-l1-yl-2,4-dioxo-imidazolidin- 1-yl }-acetylamino) -4-methylsulfanyl-butyric acid methyl ester prepared in Example 1-3) and
O.OS
3 mi (O.
26 minol) of triisopropylsilane were dissolved in 5DI of methylene chloride. Then, 5 me of trifluoroacetic acid was added thereto and the resulting solution was stirred for one hour at room temperature.
The organic solvent was removed under reduced pressure and saturated potassium carbonate [K 2 C0 3 solution was added. The solution was extracted with IOM of ethyl acetate and the solvent was removed under reduced pressure. The residue was subjected to chromatography using a solvent mixture of methanol-methylene chloride(5 :95) as the eluent to obtain 0.068g(Yield: 95%) of the title compound.
'H NMR(CDCl 3 a (ppm).1.88(2H, in), 2.00(3H, 2.06(3H, s), 9.14(2H, in), 2.45(2H, 2.76(2H, in), 3.38(1H, dd), 3.69(3H, d), 3.82(2H, in), 4.54(1H, in), 6.87(1H, 7.60-7.40(5H, in), 7.72(1H, d), 7.91(2H, in) FAB Mass(M±H) 552 WO 99/05117 WO 9905117PCT[KR98/00225 57 Example 2 Synthesis of lH-im idazol-4-yi)-propyll-5-methyl-5-n aphthalen -1 -yl-2,4-d ioxo-im id azo lid in- 1-yl}-acetyiam ino)-4-m ethylsulIfanyl-bu ty ric acid(Compound 2) lithium salt 0. 068g(O. 12 mmol) of 1H-imidazol-4-yl)-propyll-5mnethyl -5 -naphthalen- 1 -yl-2,4-dioxo-imidazolidi- Il-yl I -acetylamino)-4-methyl sulfanyl-butyric acid methyl ester prepared in Example 1 was dissolved in 4 mfle of a solvent mixture of tetrahydrofuran-distilled water(3:1).
O.005g(O. 12 mmol) of lithium hydroxide was added thereto 'and stirred for one hour. After solvents were removed under reduced pressure, the residue was thoroughly dried under vacuum to obtain 0.06g(Yield of the title compound.
ESI Mass(M+Li+) :538 Example 3 Synthesis of {3-12-(1H-im idazol-4-yl)-ethyl]-5-methyl-5-naphthalen- 1 -yl-2,4-dioxo-im idazolidin-1-yl}-acetylam ino)-4-methylsulfanyl-bu tyric acid methyl ester(Compound 3) 0.032g of the title compound was prepared according to the same procedure as Example 1 except that 2-(1-triph enylmethyl-imidazol-4-yi)ethanol was used instead of 3 -(1-triphenylethyl-imidazol-4-yl)-propanol in Example 1-1).
I HNMR(CDCl 3 3 (ppm) 1.88(2H, in), 2.01(3H, 2.08(3H, s), 2.20(LH, 2.45(1H, 3.20(2H, in), 3.37(1H, dd), 3.70(3H, d), 4.05(2H, in), 4.54(LH, in), 6.97(1H, 7.71-7.30(6H, in), 7.90(2H, m) FAB Mass(M+H) :538 WO 99/05117 PCT/KR98/00225 58- Example 4 Synthesis of lH-imidazol- 4 I -yI-2,4-dioxo-imidazolidin-1 -yI}-acetylam ino)-4-methylsu lfanyl-bu tyric acid(Compound 4) lithium salt 0.02g of the title compound was prepared according to the same procedure as Example 2 usig .03g(O.056 mmol) of imidazol-4-yl)-ethyl]-5-methyl-5-naphthalen I -yl-2,4-dioxo-imidazolidin- l-yl -acetylamino)-4-methylsulfanyl-butyric acid methyl ester prepared in Example 3 ESI Mass(M-Li++2H) :524 Example Synthesis of 2- {2-13-(311-im idazol-4-yl-methyl)-5-methyl--naphthalen..1 yl-2,4-d joxo-im idazolidin-1 -ylI-acetylamino}-4-methylsulfanyl-butyric acid methyl ester(Compound 0.025g of the title compound was prepared according to the same procedure as Example 1 except that (3-triphenylmethyl-imidazol-4-yl)methanol was used instead of I-triphenyhnethyl-imidazol-4-yI)-propanol in Example 1-1).
I1 NMR(CDC1 3 3 (ppm) 1.80(2H, in), 1.98(3H, 2.00('5H, s), 2.08(lH, 2.38(1H, 3.38(1H, dd), 3.67(3H, 4.45(1H, in), 4.88(2H, 6.80(1H, in), 7.08(3H, in), 7.34(1H, in), 7.45(IH, in), 7.68(1H, 7.82(2H, m) FAB Mass(M+1) :524 WO 99/05117 WO 9905117PCTI.KR98/00225 59 Example 6 Synthesis of 2- 12-13-(311-im idazol-4-yl-m ethyl)-5-methyl-5-naphthalen-1yl-2,4-d joxo-im idazolidin-1 -yI-acetylamino)-4-methylsulfanyl-butyric acid (Compound 6) lithium salt 0.0 15g of the title compound was prepared according to the same procedure as Example 2 using 0.02g(0.038 mmol) of imidazol-4-yl-methyl)-5-methyl-5 -naphthalen- 1-yI-2,4-dioxo-imidazolidin- l-yl ]-acetylamino}-4-methylsulfanyl-butyric acid methyl ester prepared in Example ESI Mass(M-Li++2H) :510 Example 7 Synthesis of [3-(4-cyano-benzylI)-im. idazol-4-yl-methylj-5-m ethyl- 5-naphthalen-1-yl-2,4-dioxo-imidazolidin-1 -yl}-acetylam ino)-4-m ethylsulfa nyl-butyric acid methyl ester(Com pound 7) 0.04g of the title compound was prepared according to the same procedure as Example 1 except that I imidazole prepared in Preparation 7 was used instead of 3-(1triphenylmethyl-imidazol-4-yl)-propanol in Example 1-1).
I1 NMR(CDC1 3 a (ppm) 1 .85(2H, in), 2.00(3 H, 2.06(4H, in), 2.45(1H, 3.36(LH, dd), 3.71(3H, 4.50(LH, mn), 4.71(2H, in), 5.48(2H, dd), 6.90(1H, in), 7.08(1H, in), 7. 14(2H, in), 7.39-7.75(7H, i) 7.91(2H, in) FAB Mass(M+H) :639 Example 8 WO 99/05117 WO 9905117PCT/KR98/00225 60 Synthesis of [3-(4-cyano-benzyl)-im id azol1-4-yl-m ethylj-5-m ethyl- 5-naphthalen-1-yl-2,4-dioxo-imidazolidin-1 -yI}-acetylamino)-4-niethylsulfa nyl-butyric acid(Compound 8) lithium salt 0.025g of the title compound was prepared according to the same procedure as Example 2 using 0.03g(O.047 inmol) of 2 -(2-{3-[3-(4-cyano- -methyl-5-naphthalen- 1-yl-2,4-dioxo-imidazolI din- l-yl }-acetylamino)-4-methylsulfanyl-butyric acid methyl. ester prepared in Example 7.
FAB Mass(M+H) :631 Example 9 Synthesis of {3-13-(3H-im idazol-4-yl)-propyl]-5-methyl-5-naphthalen -1 -yl-2,4-d ioxo-im id azolidin-1-yl)-acetam in o)-3-thiop hen-2-yI-p rop ionic acid(Compound 9) lithium salt 0.025g of the title compound was procedure as Example 1 and 3 -thiophen-2-yl-propionic acid methyl methionine methyl ester in Example 1-3).
prepared according to the same Example 2 except that ester was used instead of I H NMR(CD 3 OD) 8 (ppm) 1.95(3H, 2.10O(2H, in), 3.20(2H, in), 3.78(2H, 4.OO(lH, dd), 4.71(lH, in), in), 7.12(lH, in), 7.34-7.54(5H, mn), 7.59(lH, 7.99(2H, q) ESI Mass(M-Li++2H) :560 in), 2.74(2H, 6.68-6.90(3H, Example Synthesis of 3-13-(3H-im idazol-4-yl)-propylJ-5-m ethyl-5-naphthalen-1-yl- I -(2-oxo-2-th iazolidin-3-yI-ethyl)-im idazo lidin-2,4-dione(Com pound WO 99/05117 WO 9905117PCT/KR98/00225 61 0.06g of the title compound was prepared according to the same procedure as Example I except that thiazolidine was used instead of methionine methyl ester in Example 1-3).
H NMR(CDCl 3 8 (ppm) 2.02(3H, 2. 15(2H, in), 2.70(2H, t), 3.00(2H, br), 3.75(2H, 3.80(2H, 4.02(2H, in), 4.50(2H, 6.60(1H, 7.13(6H, in), 7.33(11H, in), 7.46(3H, in), 7.69(1H, 7.89(2H, m) FAB Mass(M+H) :478 Example 11 Synthesis of ,1-dioxo-th iazolidin-3-y)-3-(311-im idazol-4-yI)-propylj -5-methyl-5-naphthalen-1-yI-imidazolidin-2,4-dione(Com pound 11) 0.05g of the title compound was prepared according to the same procedure as Example 1 except that 1, 1-dioxo-thiazolidie was used instead of methionine methlyl. ester in Example 1-3).
IIH NMR(CDCl 3 8 (ppm) 2.02(3H, 2. 15(2H, in), 2.70(2H, t), 3.24(2H, 3.80(2H, 4.02(4H, mn), 4.40(2H, br), 6.60(LH, 7.13(6H, in), 7.33(11H, in), 7.46(3H, in), 7.69(lH, 7.89(2H, in) FAB Mass(M+H) :510 Example 12 Synthesis of 3-[3-(3H-im idazol-4-yI)-propyl]-5-methyl-1 12-[2-(2-m ethyl sulfanyl-ethyl)-th iazolidin-3-yl]-2-oxo-ethyl}-5-naphthalen-1-y-im idazolidi n-2,4-d ione(Comnpound 12) 0.055g of the title compound was prepared according to the same procedure as Example 1 except that 2-(2-methylsulfanyl-ethyl)-thiazolidine WO 99/05117 PTK9/02 PCT/KR98/00225 62 was used instead of methionine methyl ester in Example 1-3).
'H NMR(CDCl 3 3 (ppmn) 1.90(1H, in), 2.05(4H, in), 2.15(2H, in), 2.57(2H, mn), 2.70(2H, 2.85(2H, in), 2.96(lH, in), 3.32(JH, in), 3.80(2H-, 4.02(2H, in), 4.52(lH, 6.60(lH, 7.13(6H, in), 7.33(11H, in), in), 7.69(1H, 7.89(2H, mn) FAB Mass(M+H) :552 Example 13 Synthesis of 3 3 3 H-im idazol1-4-yl)-p ropyl11-5-m ethyl-5-n a phtha len -1 -yl-2,4-dioxo-imidazolidin-1-yl}-acetylam ino)-4-m ethylsulfonyl-bu tyric acid(Compound 13) lithium salt The same procedure as Example 1 was carried out except that 4-methyl sulfonyl-butyric acid methyl ester was used instead of methionine methyl ester in Example and then the resulting product was treated according to the samie procedure as Example 2 to obtain 0.024g of the title compound.
FAB Mass(M+H) :576 Example 14 Synthesis of 2- 2 idazol-1 -yI-propyl)-5-m ethyl-5-naphthalen-1-yl- 2,4-dioxo-imidazolidin-1-yI]-acetylamino} -4-rnethylsulfanyl-butyric acid (Compound 14) lithium salt The same procedure as Example 1 was carried out except that 3 -(iinidazol-l1-yl)-propanol prepared in Preparation 8 was used isedof 3-(1-triphenyiinethyl- imidazol-4-yl)-propanol in Example and then the resulting product was treated according to the same procedure as WO 99/05117 PCT/KR98/00225 -63 Example 2 to obtain 0.024g of the title compound.
ESI Mass(M-Li++2H) :552 Example Synthesis of 2- idazol-1-yl-ethyl)-5-methyl-5-naphthalen-1 -yl- 2,4-dioxo-imidazolidin-1-ylJ-acetylam ino}-4-m ethylsulfanyl-butyric acid (Compound 15) lithium salt The same procedure as Example 1-1) to 1-3) was carried out except that 2-(imidazol-1-yl)-ethanol prepared in Preparation 9 was used instead of triphenylinethyl-iinidazol-4-yl)-propanol in Example 1-1), and then the resulting product was treated according to the same procedure as Example 2 to obtain 0.027g of the title compound.
ESI Mass(M-Li++2H) 538 Example 16 Synthesis of 1-benzyl-3-(3-im idazol-1 -yl-p 1 -yi-imidazolidin-2,4-dione(Com pound 16) The title compound was prepared in a yield of 80% accordig to the same procedure as Example 1-1) to 1-2) except that 3 (imidazol-l-yl)-propanol was used instead of 3)-(l-triphenylmethyl-imidazol -4-yl)-propanol in Example 1-1) and that benzyl bromide was used instead of ethyl bromoacetate in Example 1-2).
1 NMR(CDC1 3 8 (ppm) 1.86(3H, 2.27(2H, in), 3.77(2H, t), 4.07-4.20(3H, in), 4.31(lH, 6.78-6.85(2H, mn), 6.87(lH, 7.03(IH, 7.09(3H, mn), 7.21(1H, 7.32(lH, in), 7.42(lH, 7.48(lH, t), WO099/05117 PCT/KB.98/00225 64 7.57(1H, 7.63(111, 7.82(1H, 7.87(1H, d) FAB Mass(M+H) :439 Example 17 Synthesis of 1 -(pentafluoro-benzyl)-3-(3-im idazol-1 -yl-p ropyl)-5-m ethyl- 5-naphthalen-1 -yI-im idazolidin-2,4-dione(Com pound 17) The title compound was prepared in a yield of 87% according to the same procedure as Example 1 except that 3-(imidazol-1-yl)-propanol prepared in Preparation 8 was used instead of 3 -triphenylmethylimidao-4-yl)-propanol in Example 1-1) and that pentafluoro-benzyl bromide was used instead of ethyl bromoacetate in Example 1-2).
I1 NMR(CDCl 3 8 (ppm) 2.10(311, 2.30(2H, in), 3.82(2H, t), 4.07-4.20(3H1, in), 5.11(111, 7.06(111, 7.12(111, 7.20(111, d), 7.35-7.50(3H, in), 7.66(1H, 7.68-7.80(311, in) FAB Mass(M+H) :529 Example 18 Synthesis of I -(3-pyridylmethyl)-3-(3-im idazol-1-yl-propyl)-5-m n aph thalen-1 -yl-im idazo lid in-2,4-dione(Cominpound 18) The title compound was prepared in a yield of 60% according to the same procedure as Example I except that 3-(imidazol- 1-yl)-propanol prepared in Preparation 8 was used instead of 3-(1-triphenylmethylimidazol-4-yl)-propanol in Example 1-1) and that 3-pynidylmethyl chloride was used instead of ethyl bromoacetate in Example 1-2).
'H NMR(CDC1 3 8 (ppm) 1.89(3H1, 2.30(2H, in), 3.81(2H, in), 4.15(31H, in), 4.35(111, 6.85(111, in), 7.08-7.52(7H, in), 7.65(111, d), WO 99/05117 WO 9905117PCT/KR98/00225 65 7.85(3H, in), 7.98(1H, 8.21(1H, d) FAB Mass(M+H) :440 Example 19 Synthesis of 1-(3-chloro-benzyl)-3-(3-im idazol-1-yl-propyl)-5-m naphthalen-1-yI-imidazolidin-2,4-dione(Compound 19) The title compound was prepared in a yield of 90% according to the same procedure as Example I except that 3-(imidazol- 1-yl)-propanol prepared in Preparation 8 was used instead of 3-(l-triphenylmethylimidazol-4-yl)-propanol in Example 1-1) and that 3-chlorobenzyl bromide was used instead of ethyl bromoacetate in Example 1-2).
1 H NMR(CDCI 3 a (ppm) 1.86(3H, 2.27(2H, in), t), 4.02(1H, 4.10(2H, 4.35(1H, 6.76(2H, in), 6.90(lH, 6.97(1H, 7.06(lH, 7.11(1H, 7.21(lH, 7.32(1H, 7.42(1H, t), 7.50(1H, 7.63(IH, 7.68(lH, 7.82(1H, 7.88(1H, d) FAB Mass(M+H) :473 Example Synthesis of 1-(3-brom o-benzyl)-3-(3-imidazol-1-yI-propyl)-5-m n aph th alen-1-yi-imidazo lid in-2,4-d ione(C omipound The title compound was prepared in a yield of 90% accordig to the same procedure as Example 1 except that 3'-(I'MIdazol- I-yl)-propanol prepared in Preparation 8 was used instead of 3-(1-triphenylmethylimidazol-4-yl)-propanol in Example 1-1) and that 3-broino-benzyl bromide was used instead of ethyl broinoacetate in Example 1-2).
1 HNMR(CDCl 3 8 (ppm) 1.86(3H, 2.27(2H, in), 3.77(214, t), WO 99/05117 WO 9905117PCT/KR98OO225 66 4.07-4.20(3H, in), 4.31(1H, 6.78-6.85(2H, in), 6.87(LH, 7.03(1H, 7.09(2H, in), 7.21(1H, 7.32(1H, in), 7.42(1H, 7.48(1H, t), 7.57(1H, 7.63(1H, 7.82(1H, 7.87(1H, d) FAB Mass(M+H) :517 Example 21 Synthesis of I-( 4 -bromo-benzyl)-3-(3-imidazol-1 -yl-propyl)-5-m naphthalen-1-yi-im idazolidin-2,4-dione(Com pound 21) The title compound was prepared in a yield of 95% according to the same procedure as Example 1-1) to 1-2) except that 3-(imidazol-1yl)-propanol prepared in Preparation 8 was used instead of 3-(1triphenylmethyl-imidazol-4-yl)-propanol in Example 1-1) and that 4-bromo -benzyl bromide was used instead of ethyl bromoacetate in Example 1-2).
1 H NMR(CDCl 3 8 (ppm) 1.86(3H, 2.27(2H, in), 3'.77(2H, t), 3.97(1H, 4.09(2H, 4.3 1(1H, 6.72(2H, 7.05(LH, 7.10(3H, in), 7.23(1H, 7.32(1H, 7.41-7.55(2H, in), 7.57-7.68(2H, in), 7.86(1H, 7.89(1H, d) FAB Mass(M+H) :517 Example 22 Synthesis of 1 -(3-trifluorom ethyl-benzyl)-3-(3-imidazol-1 m ethyl-5-nap hthalen-1 -yl-im idazolid in -2,4-dion e(Com pou nd 22) The title compound was prepared in a yield of 92% according to the same procedure as Example 1-1) to 1-2) except that 3-(imidazol-1yl)-propanol prepared in Preparation 8 was used instead of 3 triphenylmethy1-lnidazol-4-yl)-propanol in Example 1-1) and that 3-trifluoromethyl-benzyl bromide was used instead of ethyl bromoacetate in WO 99/05117 WO 9905117PCT/KR98/00225 67 Example 1-2).
'H NMR(CDCI 3 (3(ppm) 1.86(3H, 2.30(2H, in), 3.80(2H, in), 4.10(2H, 4.30(2H, 6.94(IH, 7.00-7.15(4H, in), 7.20(1H, t), 7.29(IH, 7.40(1H, 7.48(lH, 7.62(1H, 7.72(1H, 7.78(1H, 7.85(IH, d) FAB Mass(M+H) :507 Example 23 Synthesis of 1-(3-trifluoromethoxy-benzyl)-3-(3-im idazol-1 mnethyl-5-naphthalen-1 -yI-im idazolidin-2,4-dione(Com pound 23) The title compound was prepared in a yield of 80% according to the same procedure as Example 1-1) to 1-2) except that 3-(imidazol- I -yl)-propanol prepared in Preparation 8 was used instead of 1triphenylinethyl-imidazol-4-yl)-propanol in Example 1-1) and that 3-trifluoromethoxy-benzyl bromide was used instead of ethyl bromoacetate in Example 1-2).
1H NMR(CDCl 3 3 (ppm) 1.80(3H, 2.30(2H, in), 3.80(2H, in), 4.0O(1H, 4.10(2H, 4.44(1H, 6.72(1H, 6.79(1H, 6.89(1H, 7.00(1H, 7.06(1H, 7.1O(1H, 7.22(1H, 7.33(1H, t), 7.43(1H, 7.49(LH, 7.62(1H, 7.67(1H, 7.83(1H, 7.88(1H, d) FAB Mass(M+H) :523 Example 24 Synthesis of 3-(3-im idazol-1 -yI-propyl)-5-m ethyl-5-naphthalen-1 -yl-l-(4p hen oxy-benzyl)-im idazolidin-2,4-d ione(Com pound 24) WO 99/05117 PCT/KR98/00225 68 The title compound was prepared in a yield of 70% according to the same procedure as Example 1-1) to 1-2) except that 3-(imidazol- 1 -yl)-propanol prepared in Preparation 8 was used instead of 3 -tripheniyhnethyl-iinidazol-4-yl)-propanol in Example 1-1) and that 4-phenoxy-benzyl bromide was used instead of ethyl bromoacetate in Example 1-2).
1H NMR(CDCI 3 8 (ppm) 1.86(3H, 2.27(2H. in), 3).73-3).85(3
H,
in), 4.09(2H, 4.57(1H, 6.61(1H, 6.73(2H, 6.88(2H, d), 7.04(2H, in), 7.10(2H, in), 7.25-7.40(4H, in), 7.43-7.50(2H, in), 7.56-7.63(2H, in), 7.89(2H, t) FAB Mass(M+H) :531 Example Synthesis of 3 3 -imidazol-1-yl-propyl)-5-methyl-5-naphthalen-1 -yI-l-(3phenoxy-benzyl)-im idazolid in-2,4-dione(Co mpound The title compound was prepared in a yield of 73% accordig to the same procedure as Example 1-1) to 1-2) except that 3-(imidazol- 1 -yl)-propanol prepared in Preparation 8 was used instead of 3 -triphenyhnethyl-imidazol-4-yl)-propanol in Example 1-1) and that 3-phenoxy-benzyl bromide was used instead of ethyl bromoacetate in Example 1-2).
1 NMR(CDC1 3 3 (ppm) 1.86(3H, 2.27(2H, mn), 3.73'-3.85(3H, in4.09(2H, 4.57(1H, 6.60(1H, 6.72(2H, 6.88(2H, d), 7.00-7.12(4H, mn), 7.25-7.40(4H, mn), 7.43-7.50(2H, in), 7.57(1H, s), 7.60(1H, 7.89(2H, t) FAB Mass(M+H) :531 WO099/05117 PCT/KR98/00225 -69 Example 26 Synthesis of 3-(3-imidazol-1-yl-propyl)-1 -(4-rnethylsu in ethyl-5-naphthalen-I -yl-im idazolidin-2,4-d ione(Com pound 26) The title compound was prepared in a yield of 85% according to the same procedure as Example 1-1) to 1-2) except that 3-(imidazol- I -yl)-propanol prepared i Preparation 8 was used instead of 3 -triphenyhnethyl-imidazol-4-yl)-propanol in E xample 1-1) and that 4-methylsulfanyl-benzyl bromide was used instead of ethyl bromoacetate in Example 1-2).
1H NMR(CDCl 3 8 (ppm) 1.86(3H, 2.27(2H, 3.73-3.85(3H, in), 4.09(2H, 4.57(1H, 6.88(2H, 6.99(2H, 7.04(1H, s), 7.08(1H, 7.29(1H, 7.34(1H, 7.45(1H, 7.51(1H, 7.58(1H, 7.62(1H, 7.86(1H, 7.90(1H, d) FAB Mass(M+H) :485 Example 27 Synthesis of 3-(3-imidazol-1-yI-propyl)-1-(4-m ethylsulfanylmethyl-benzyl) -5-methyl-5-naphthalen-1 -yl-imidazolid in-2,4-dione(Com pound 27) The title compound was prepared in a yield of 65% according to the same procedure as Example 1-1) to 1-2) except that 3-(imidazol- 1-yl)-propanol prepared in Preparation 8 was used instead of 3 -triphenyhnethyl-imidazol-4-yl)-propanoI in Example 1-1) and that 4-methylsulfanylmethyl-benzyl bromide was used instead of ethyl bromoacetate in Example 1-2).
1 H NMR(CDCI 3 8 (ppm) 1.86(3H, 2.27(2H, mn), 3.55(2H, s), 3.73-3.85(3H, in), 4.09(2H, 4.57(lH, 6.88(2H, 6.99(2H, d), WO 99/05117 WO 9905117PCT/KR98/00225 70 7.04(111, 7.08(111, 7.29(1H, 7.34(111, 7.45(1.H, 7.51(IH, 7.58(111, 7.62(111, 7.86(111, 7.90(11H, d) FAB Mass(M+H) :499 Example 28 Synthesis of 3-(3-im idazol-1-yI-propyl)-1-(4-methylsu m ethyl-5-naphthalen-1-yl-imidazolidin-2,4-d ione(Com pound 28) The title compound was prepared in a yield of 70% according to the same procedure as Example 1-1) to 1-2) except that 3-(imidazol- I -yl)-propanol prepared in Preparation 8 was used instead of 3 -triphenylmethyl-imidazol-4-yl)-propanoI in Example 1- 1) and that 4-methylsulfonyl-benzyl bromide was used instead of ethyl bromoacetate in Example 1-2).
H NMR(CDC1 3 a (ppm) 1.86(3H, 2.27(2H, in), 2.87(3H, s), 3.80(2H, 4.09(2H1, 4.25(111, 4.40(1H, 6.95(2H1, 7.04(1H, 7.08(1H, 7.18(1H, 7.28(111, 7.37-7.45(4H, mn), 7.59(1H, s), 7.64(IH, 7.77(111, 7.83(1H, d) FAB Mass(M+H) :517 Example 29 Synthesis of 5-1 3 3 -imidazol-1-yI-propyl)-5-methyl-5-naphthalen-1 -yl- 2,4-dioxo-im idazo lid in-1 -ylm ethyll-2-m ethylsulIfanyl-benzo nitrile(Comn po u nd 29) The title compound was prepared in a yield of 50% according to the same procedure as Example 1-1) to 1-2) except that 3 -(imidazol- I -yl)-propanol prepared in Preparation 8 was used instead of .3 -triphenylmethyl-imidazol-4-yl)-propanol in Example 1-1) and that WO 99/05117 WO 9905117PCT/KR98/00225 71 -bromomethyl-2-methylsulfanyl-benzonitrile was used instead of ethyl bromoacetate in Example 1-2).
1H NMR(CDC 3 8 (ppm) 1.86(3H, 2.27(2H, in), 2.40(3H, s), 3.80(2H, 4.0O(1H, 4.09(2H, 4.48(1H, 6.66(1H, 6.69(1H, 6.95(1H, dd), 7.04(1H, 7.05-7.12(2H, in), 7.25(1H, 7.40(1H, t), 7.49(1H, 7.59(1H, 7.64(1H, 7.78(1H, 7.87(1H, d) FAB Mass(M+H) :5 Example Synthesis of 5-13-(3-imidazol-1 -yI-propyl)-5-methyl-5-naphthalen- l-yI- 2,4-dioxo-im idazolidin-I -ylmethylJ-2-methylsulfonyl-benzonitrile(Com pou nd The title compound was prepared in a yield of 72% according to the same procedure as Example 1-1) to 1-2) except that 3-(imidazol- 1 -yl)-propanol prepared in Preparation 8 was used instead of 3 -triphenylinethyl-iinidazol-4-yl)-propanol in Example 1-1) and that -bromomethyl-2-methylsulfonyl-benzonitrile was used instead of ethyl bromoacetate in Example 1-2).
1 H NMR(CDC1 3 8 (ppm) 2.10(3H, 2.32(2H, in), 3.08(3H, s), 3.83(2H, mn), 3.95(1H, 4.15(2H, 4.85(1H, 6.92(1H, s), 7.02-7.06(2H, in), 7.10-7.14(2H, in), 7.28(1H, 7.41(1H, 7.49(LH, d), 7.52(1H, 7.61(1H, 7.69(1H, 7.77(1H, 7.86(IH, d) FAB Mass(M+H) :542 Example 31 Synthesis of 2-[3-(3-im idazol-1-yl-propyl)-5-methyl-5-naphthalen-1 -yl-2,4 -dioxo-imidazolidin-1-ylm ethyll-benzonitrile(Com pound 31) WO099/05117 PCT/KR98/00225 72 The title compound was prepared in a yield of 90% according to the same procedure as Example 1-1) to 1-2) except that 3-(imidazol- 1-yl)-propanol prepared in Preparation 8 was used instead of 3-(1-triphenytmethyl-imidazol-4-yl)-propanol in Example 1-I) and that 2-bromomethyl-benzonitrile was used instead of ethyl bromoacetate, in Example 1-2).
'H NMR(CDCl 3 a (ppm) 1.86(3H, 2.30(2H, in), 3.80(2H, in), 4.09(2H, 4.43(1H, 4.73(1H, 6.89(1H, in), 6.95(1H, in), 7.03-7.10(4H, in), 7.22(1H, 7.30(1H, in), 7.36(LH, in), 7.43(1H, t), 7.59(1H, 7.67(1H, 7.70(2H, d) FAB Mass(M+H) :464 Example 32 Synthesis of 3-[3-(3-im idazol-1 -yI-propyl)-5-methyl-5-naphthalen-1 -yI-2,4 -d ioxo-im idazolidin- 1-ylm ethyl]-benzon itrile(Com pound 32) The title compound was prepared in a yield of 80% according to the same procedure as Example 1-1) to 1-2) except that 3-(imidazol- 1 -yl)-propanol prepared in Preparation 8 was used instead of 3 -triphenylmethyl-imidazol-4-yl)-propanol in Example 1-1) and that 3-bromomethyl-benzonitrile was used instead of ethyl bromoacetate in Example 1-2).
I H NMR(CDCl 3 8 (ppm) 1.86(3H, 2.30(2H, in), 3.80(2H, t), 4.05-4.20(3H, mn), 4.42(lH, 6.84(1H, 6.97(1H, 7.04(1H, s), 7.06-7.19(4H, mn), 7.29(1H, mn), 7.41(1H, 7.51(1H, 7.59(111, s), 7.67(lH, 7.80(lH, 7.89(lH, d) FAB Mass(M+H) :464 WO 99/05117 WO 9905117PCT/KR98/00225 73 Example 33 Synthesis of 4-[3-(3-imidazol-1 -yI-propyl)-5-methyl-5-naphthalen-1 -yl-2,4 -d ioxo-imrnidazolid in-1 -ylm ethyll1-benzon itrile(Com pou nd 33) The title compound was prepared in a yield of 77% according to the same procedure as Example 1-1) to 1-2) except that 3-(imidazol..
I -yl)-propanol prepared in Preparation 8 was used instead of .3 -(1I -triphenyhnethyl-imidazol-4-yl)-propanol in Example 1-1) and that 4-bromomethyl-benzonitrile was used instead of ethyl bromoacetate in Example 1-2).
H NMR(CDCl 3 a' (ppm) 2. 10(3H, 2.32(2H, in), 3.08(3H, s), 3.83(2H, in), 3.95(1H, 4.15(2H4, 4.85(LH, 6.92(]H4, s), 7.02-7.06(2H4, in), 7.10-7.14(2H4, in), 7.28(114, 7.41(IH, 7.49(1H, d), 7.52(1H, 7.61(1H, 7.69(1H, 7.77(114, 7.86(114, d) FAB Mass(M+H) :542 Example 34 Synthesis of l-( 4 -aminomethyl-benzyl)-3-(3 m ethyl-5-naphthalen-1-yI-im idazolidin-2,4-d ione(Compound 34) The title compound was prepared in a yield of 80% according to the same procedure as Example 1 except that 3-(imidazol-1 -yl)-propanol prepared in Preparation 8 was used instead of 3-(1-triphenylmethyl -imidazol-4-yl)-propanol in Example 1-I) and that 4-[N-(t-butyloxy -carbonyl)-aminomethyl]-benzyl bromide was used instead of ethyl bromoacetate in Example 1-2).
1 H NMR(CDCl 3 a (ppm) 1.88(3H4, 2.29(2H4, in), 2.80(3H, s), WO 99/05117 WO 9905117PCT/KR98/00225 74 3.58(2H, 3.79(2H, in), 3.91(LH, 4.09(2H, 4.44(1H, 6.86(2H, 6.98(2H, 7.06(2H, in), 7.25(1H, 7.33(1H, 7.44(1H, t), 7.48(1H, 7.57(1H, 7.60(LH, 7.83(1H, 7.88(1H, d) FAB Mass(M+H) 468 Example Synthesis of N- {2-13-(3-imidazol-1 -yl-propyl)-5-m ethyl-5-naphthalen-1 -yI- 2 4 -dioxo-im idazo lid in-1I-ylm eth yll-benzyl I-meth anesulfo nam ide(Co mpo u nd 35-1) Synthesis of 1 -(2-amninomethyl-benzyl)-3-(3 -iinidazol- 1-yl-propyl) 1-yl-unidazolidin-2,4-dione The title compound was prepared in a yield of 83% according to the same procedure as Example 34 except that 2-[N-(t-butyloxycarbonyl) -ainomethyl]-benzylbroinide was used instead of 4-[N-(t-butyloxy -carbonyl)-aininomethyl]-benzylbroniide.
35-2) Synthesis of -imidazol- 1-yl-propyl)-5-methyl-5-naphthalen -l -yl-2,4-dioxo-imnidazolidin- 1-ylinethyl }-benzyl]-methanesulfonamide 0.02 ml (0.24 minol) of methansulfonyl chloride was added to ml dichioromethane solution of 0.06 ml (0.4 iniol) of triethylamine and 0.10 g (0.2 mmol) of l-( 2 -amninomethyl-benzyl)-3-(3-imidazol-1yl.propyl) -5-methyl-5-naphthalen-l1-yl-imidazolid'm-2,4-dione prepared in Example 3 5-1) at After stirring for 1 hour at room temperature, it was washed with saturated potassium carbonate solution and saturated sodium chloride solution sequentially. After removal of dichioroinethane, chromatography using a solvent mixture of inethanol-dichloroinethane (7:93) as the eluent was carried out to obtain 0.1 g (0.18 inmol, Yield: 87%) of the title compound.
WO 99/05117 WO 9905117PCT/KR98/00225 75 'H NMR(CDCl 3 a (ppm) 1.76(3H, 2.29(2H, in), 2.78(3H, s), 3.79(2H, 4.04(lH, 4.10(2H, 4.16(2H, 4.67(lH, 6.55(1H, 6.95(lH, 7.04-7.18(4H, in), 7.25(lH, in), 7.40(lH, 7.44-7.55(2H, in,7.60(2H, in), 7.85(lH, 7.90(lH, d) FAB Mass(M±H) :546 Example 36 Synthesis of N- {3-13-(3-imidazol-1-yI-propyl)-5-m ethyl-5-naphthalen-1-yI- 2,4-d ioxo-im idazo lid in- I-ylm ethylj-benzyl}-m eth anesulfo nam ide(Co mpou nd 36) The title compound was prepared in a yield of 78% according to the same procedure as Example 35 except that 3-[N-(t-butyloxy -carbonyl)-aminomethyl]-benzylbromide was used instead of 4-[N-(t-butyloxycarbonyl)-aininomethyl] -benzylbromide.
'H NMR(CDCl 3 6 (ppm) 1.63(3H, 2.23-2.43(2H, in), 2.85(3H, 3.85-3.93(3H, mn), 4.02-4.21(4H, mn), 4.50(1H, 6.78(1H, d), 6.99(2H, 7.06(3H, in), 7.18(1H, in), 7.37(lH, in), 7.46(lH, t), 7.50(lH, 7.58(lH, 7.63(1H, 7.87(lH, 7.89(1H, d) FAB Mass(M±H) :546 Example 37 Synthesis of N- 4 3 -(3-imidazol-1-yI-propyl)-5-m ethyl-5-naphthalen-1 -yl- 2 4 -dioxo-imidazolidin-1-ylmethyll-benzyl}-methanesulfonamide(Compou nd 37) The title compound was prepared in a yield of 83% according to the same procedure as Example 35-2) except that 1 -(4-aminomethyl-benzyl)-3 -imidazol- 1-yl-propyl)-5-inethyl-5-naphthalen- 1 WO 99/05117 WO 9905117PCT/KR98/00225 76 -yl-imidazolidin-2,4-dione prepared in Example 34 was used instead of 1 -(2-aminomethyl-benzyl)-3-(3 -imidazol- 1-yl-propyl)-5-.methyl-5-naphthalen-
I
-yl-imidazolidmn-2,4-dione.
I H NMR(CDCl 3 8 (ppm) 1.88(3H, 2.29(2H, in), 2.80(3H, s), 3.79(2H, in), 3.91(1H, 4.05-4.15(4H, in), 4.44(1H, 6.86(2H, d), 6.98(2H, 7.06(2H, 7.25(1H, 7.33(1H, 7.44(1H, 7.48(1H, 7.57(lH, 7.60(1H, 7.83(1H, 7.88(1H, d) FAB Mass(M+H) :546 Example 38 Synthesis of 4-[3-(3-imidazol-1 -yl-propyl)-5-methyl-5-naphthalen-1 -yI- 2,4-dioxo-imidazolidin-1-ylmethyll-benzoic acid methyl ester(Com pound 38) The title compound was prepared in a yield of 71% according to the samne procedure as Example 1-1) to 1-2) except that 3-(imidazol- 1 -yl)-propanol prepared in Preparation 8 was used instead of 3 -triphenylinethyl-imidazol-4-yl)-propanol in Example 1- 1) and that 4-bromomethyl-benzoic acid methyl ester was used instead of ethyl bromoacetate in Example 1-2).
1H NMR(CDC1 3 a (ppm) 1.80(3H, 2.28(2H, in), 2.72(2H, in), 3.79(3H, 3.95(1H, 4.08(2H, 4.48(lH, 6.94(2H, 7.03(1H, 7.lO(1H, 7.25(1H, 7.35(1H, 7.45(2H, in), 7.60(1H, d), 7.65(1H, 7.68(2H, 7.82(LH, 7.88(111, d) FAB Mass(M+H) :497 Example 39 Synthesis of 4-13-(3-im idazol-l-yl-propyl)-5-methyl-5..naphthalen-1-yl-2,4 WO 99/05117 WO 9905117PCT/.KR98/00225 77 -dioxo-imidazolidin-1-ylmethylj-benzoic acid(Compound 39) The title compound was prepared in a yield of 93% according to the same procedure as Example 2 using 4 3 -(3-imidazol-1-yl-propyl)- -methyl-5-naphthalen- 1-yl-2,4-dioxo-imidazolidin- 1-ylmethyl]-benzoic acid methyl ester prepared in Example 38.
H NMR(CDC 3 a (ppm) 483 Example Synthesis of 3-(3-im idazol-1 -yI-propyl)-1 -13-(mo rpholine-4-ca rbonyl)b enzylj-5-m ethyl-5-naphth alen- 1 -yI-im id azo lid in-2,4-dion e(Com pou nd The title compound was prepared in a yield of 90% from compound 38 according to the same procedure as Example 1-3) except that morpholine was used instead of methionie methyl ester.
H NMR(CDC1 3 a (ppm) 1.89(3H, 2.3 8(2H, in), 3.20-3.88(1OH, br), 4.13(1H, 4.45(1H, 6.92(2H, 7.30(2H, d), 7.33(LH, 7.35(3H, in), 7.41(1H, 7.50(1H, 7.65(1H, 7.82(1H, 7.88(1H, 9.30(1H, s) FAB Mass(M+H) :552 Example 41 Synthesis of 4-[3-(3-imidazol-1 -yI-propyl)-5-methyl-5-naphthalen-1 -yI- 2,4-dioxo-im idazolidin-1-ylmethyll-N-(2-methoxy-ethyl)-benzam ide(Com p ound 41) The title compound was prepared in a yield of 80% from compound 38 according to the same procedure as Example 1-3) except WO 99/05117 WO 9905117PCT/KR98/00225 78 that 2-methoxyethylamine was used instead of mnethionme methyl ester.
I HNMR(CDCI 3 8 (ppm) 1.85(3H, 2.35(2H, in), 3.40(3H-, s), 3.61(4H, in), 3.80(2H, in), 4.O1(1H, 4.35(2H, in), 4.52(1H, d), 6.40(lH, 6.93(2H, 7.21(LH, 7.30-7.53(7H, in), 7.62(JH, d), 7.84(1H, 7.89(lH, 8.92(lH, s) FAB Mass(M+H) :540 Example 42 Synthesis of 4-13-(3-imidazol-1 -yl-propyl)-5-methyl-5-naphthalen-1 -yl-2,4 -d ioxo-imidazolidin-1-ylm ethyll-N-(2-m ethoxy-ethyl)-N-m ethyl-benzam ide (Compound 42) The title compound was prepared in a yield of 90% from compound 39 according to the same procedure as Example 1-3) except that 2-methoxy-ethylmethylamine was used instead of methionine methyl ester.
H NMR(CDCI 3 6'(ppm) 1.80(3H, 2.35(2H, in), 2.85(2H, s), 3.05(1H, 3.35(5H, in), 3.55-4.05(5H, in), 4.28(2H, in), 4.50(lH, in), 6.93(4H, 7.10(2H, in), 7.28(3H, in), 7.36(1H, 7.45(LH, in), 7.51(1H, 7.63(1H, 7.89(2H, in), 8.75(1H, s) FAB Mass(M+H) :554 Example 43 Synthesis of 4 4 3 3 -imidazol-l-yl-propyl)-5-methyl-5-naphthalen-1 -yI- 2,4-dioxo-im idazolidin-1-ylmethylj-benzoyl}-piperazine-1 -carboxylic acid benzyl ester(Compound 43) The title compound was prepared in a yield of 70% from WO 99/05117 WO 9905117PCT/KR98/00225 79 compound 38 according to the samne procedure as Example 1-3) except that piperazine 1 -carboxylic acid benzyl ester was used instead of methionie methyl ester.
IH NMR(CDC 3 8 (ppm) 1.89(3H, 2.35(2H, in), 3.10-3.75(8H, br), 3.80(2H, in), 4.19(3H, in), 4.40(lH, 5.17(2H, 6.92(2H, d), 7.01(2H, 7.18(2H, 7.24(1H, 7.28-7.44(7H, in), 7.49(1H, t), 7.63(1H, 7.82(1H, 7.89(1H, 8.20(1H, s) .FAB Mass(M+H) :685 Example 44 Synthesis of 3-(3-imidazol-1-yl-propyl)-1-13-(thiomorpholine-4-carbonyl)ethyl-5-naphthalen-1-yi-imidazolidin-2,4-dione(Compound 44) The title compound was prepared in a yield of 86% from 3 )-iiidazol- 1-yl-propyl)-5-methyl-5-naphthalen- 1-yl-2,4-dioxo-imidazolI din-i -ylmethyl]-benzoic acid methyl ester according to the same procedure as Example 1-3) except that thioinorpholine was used instead of methionine methyl ester.
'H NMR(CDC 3 a (ppm) 1.82(3H, 2.35(2H, in), 2.55(4H, br), 3.45(2H, br), 3.80(5H, in), 4.26(2H, in), 4.54(1H, 7.00(2H, in), 7.09(2H, 7.25(3H, in), 7.63(1H, 7.89(2H, 8.51(1H, s) FAB Mass(M+H) :568 Example Synthesis of 4- {5-[3-(4-methyl-4-naphthalen-1 -yl-2,5-dioxo-im idazolidin- 1 -yl)-p ropylj-im idazol-1-ylm ethyl) benzonitrile(Com pound The title compound was prepared in a yield of 60% according to WO 99/05117 PCT1KR98/00225 80 the same procedure as Example 1-1) except that 4 -IjS-(3-hydroxy-propyl)imidazol- I-ylmethyl]-benzonitrile was used instead of 3 -triphenylm ethylimidazol-4-yl)-propanol.
H NMR(CDCl 3 8 (jpm) 1.95(2H, in), 1.98(3H, 2.36(2H, t), 3.63(2H4, 5.00(2H, 6.87(1H, 6.94(2H, 7.39(2H, 7.45(3H, in), 7.53(1H, 7.63(1H, 7.83(1H, 7.88(1H, 7.90(lH, d) FAB Mass(M+H) :464 Example 46 Synthesis of 4- {5-13-(3-methyl-4-methyl-4-naphthalen-1-yl-2,5-dioxoimidazolidin-1-yI)-propyl]-im idazol-1-ylmethyl}-benzonitrile(Compound 46) The title compound was prepared in a yield of 75% according to the same procedure as Example 1-1) to 1-2) except that hydroxy-propyl)-imidazol- 1-yhnethyl]-benzonitrile was used instead of 3 -triphenylinethyl-imidazol-4-yl)-propanol in Example 1-1) and that methyl iodide was used instead of ethyl bromoacetate in Example 1-2).
'H NMR(CDC1 3 8 (ppm) 1.95(3H, 2.05(2H, 2.47(2H, t), 2.62(3H, 3.74(2H, mn), 5.16(2H, dd), 7.03(1H, 7.06(2H, d), 7.23(lH, 7.35(1H, 7.43(LH, 7.47(1H, 7.52(1H, 7.66(LH, 7.90(2H, mn), 8.24(1H, s) FAB Mass(M+H) :478 Example 47 Synthesis of 4- {5-13-(3-ethyl-4-methyl-4-naphthalen-1-yl-2,5-dioxoim idazolidin-1 -yl)-propyl]-im idazol-1 -ylm ethyl) benzonitrile(Compound 47) WO 99/05117 WO 9905117PCT/KR98/00225 81 The title compound was prepared in a yield of 78% according to the same procedure as Example 46 except that ethyl iodide was used instead of methyl iodide.
I HNMR(CDCl 3 3 (ppm) 0.83(3H, 1.95(3H, 2.07(2H, t), 2.51(2H, 3.11(2H, in), 3.76(2H, in), 5.28(2H, dd), 7.13(3H, d), 7.20(lH, 7.32(lH, 7.42(lH, 7.47(2H, 7.53(lH, 7.70(lH, 7.90(1H, 7.92(lH, 9.04(lH, s) FAB Mass(M+H) :492 Example 48 Synthesis of 4- {5-[3-(3-propyl-4-methyl-4-naphthalen-1-yI-2,5-dioxoim idazolidin-1 -yl)-propyl]-im idazol- I-ylm ethyl}I benzon itrile(Com pound 48) The title compound was prepared in a yield of 62% according to the same procedure as Example 46 except that propyl iodide was used instead of methyl iodide.
I H NMR(CDCI 3 3 (ppm) 0.61l(3H, 1.25(2H, in), 1.93(3H, s), 2.07(2H, 2.47(2H, 2.96(2H, in), 3.73(2H, in), 5.13(2H, dd), 7.04(2H, 7.22(lH, 7.32(lH, 7.41(lH, 7.68(lH, 7.90(2H, in), 7.99(1H, s) FAB Mass(M+H) :506 Example 49 Synthesis of 4- {5-[3-(3-butyl-4-methyl-4-naphthalen-1 zolidin-1I-yl)-p ro pylJ-im idazol-1 -ylm ethyl) benzon itrile(C om pound 49) WO 99/05117 WO 9905117PCT/KR98/00225 82 The title compound was prepared in a yield of 61% according to the same procedure as Example 46 except that butyl iodide was used instead of methyl iodide.
H NMR(CDC 3 8 (ppm) 0.61(3H, 1.03(2H, in), 1.24(2H, in), 1.93(3H, 2.07(2H, in), 2.47(2H, 2.99(2H-, in), 3.72(2H, in), 5.09(2H, dd), 7.00(1H, 7.03(2H, 7.22(1H, 7.32(1H, 7.42(1H, 7.48-7.53(3H, in), 7.68(1H, 7.83(1H, 7.88(1H, 7.91(]H, d) FAB Mass(M+H) :520 Example Synthesis of {3-13-(2-methoxy-ethoxym ethyl)-4-methyl-4-naphthalen- I -yl-2,5-dioxo-im idazolidin-l-ylJ-propyl)-im idazol-1-ylmethyl)-benzon itrile (Compound The title compound was prepared in a yield of 55% according to the same procedure as Example 46 except that 2-inethoxy-ethoxymethyl bromide was used instead of methyl iodide.
I H NMR(CDCI 3 8 (ppm) 2.15(3H, 2.3 1(2H, in), 3.30(4H, br), 3.41(1H, br), 3.56(1H, br), 3.70(1H, br), 3.76(2H, 4.16(3H, in), 4.98(1H, 7.09(1H, 7.13(1H, 7.28(LH, in), 7.40(1H, t), 7.45-7.60(2H, mn), 7.80(1H, 7.85-8.0(3H, in) FAB Mass(M+H) :437 Example 51 Synthesis of t3- 13-(4-cyanobenzyl)-3H-imidazol-4-yI]-propyl}-5-m ethyl -5-naphthalen-1-yI-2,4-dioxo-imidazolidin-1 -yl)-acetic acid ethyl ester (Compound 51) WO 99/05117 WO 9905117PCT/KR98/00225 83 The title compound was prepared in a yield of 88% according to the same procedure as Example 1-1) to 1-2) except that hydroxy-propyl)-imidazol- 1-ylmethyl] -benzonitrile was used instead of -triphenylmethyl-imidazol-4-yl)-propanol in Example 1-1).
IH NMR(CDCl 3 8 (ppm) 1.88(3H, 2. 12(2H, in), 2.54(2H, mn), 3.80(2H, in), 4.1O(1H, 4.39(1H, 5.20(2H, 6.88(1H, 6.96(lH, 7.03-7.22(7H, in), 7.36(1H, 7.48-7.57(3H, in), 7.66(1H, 7.80(IH, 7.89(1H, 8.11(1H, br) FAB Mass(M+H) 579 Example 52 Synthesis of [3-(4-cyanobenzyl)-3H-im idazol-4-ylJ-p ropyl}-5-m ethyl -5-naphthalen-1-y-2,4-dioxo-imidazolid in-1-yl)-acetic acid lithium salt (Compound 52) The title compound was prepared i a yield of 81% according to the same procedure as Example 1-1) to 1-2) and Example 2 except that 4- -hydroxy-propyl)-imidazol- 1 -ylm ethyl] -beuzonitrile was used instead of 3-(1-triphenylmethyl-imnidazol-4-yl)-propanol in Example 1-1).
FAB Mass(M+H) :522 Example 53 Synthesis of 4-(5-{3-13-benzyl-4-methyl-4-naphthalen-1 im idazolidin-1 -ylJ-propyl}-imidazol-1 -ylmethyl)-benzonitrile(Com pound 53) The title compound was prepared in a yield of 81% according to the same procedure as Example 1-1) to 1-2) except that 4-15-(3-hydroxy- WO 99/05117 WO 9905117PCT/KR98/00225 84 propyl)-imidazol-1-ylmethyl]-benzonitrile was used instead of 3-(l triphenylmethyl-imidazol-4-yl)-propanol in Example 1-1) and that benzyl bromide was used instead of ethyl bromnoacetate in Example 1-2).
IH NMR(CDC 3 8 (ppm) 1.68(3H, 2.09(2H, 2.50(2H, t), 3.76(3H, in), 4.75(LH, 5.23(2H, 6.90(2H, 7.06-7.22(8H, in), 7.38(1H, 7.45(3H, in), 7.59(1H, 7.85(1H, 7.90(1H, 8.46(1H, s) FAB Mass(M+H) :554 Example 54 Synthesis of 4 -(5-1 3 3 3 -cyano-benzyl)-4-methyl-4-naphthalen-1 d joxo-im idazolidin-1-yl]-p ropyl}-im idazol-l -ylm ethyl)-benzon itrile(Com po und 54) The title compound was prepared in a yield of 89% according to the same procedure as Example 1-1) to 1-2) except that hydroxy-propyl)-imidazol-l-yhnethyl]-benzonitrile was used instead of 3 -triphenylinethyl-imidazol-4-yl)-propanol in Example 1-1) and that 3-bromomethylbenzonitrile was used instead of ethyl bromoacetate in Example 1-2).
H NMR(CDCl 3 3 (ppm) 1.88(3H, 2.12(2H, in), 2.54(2H, in), 3.80(2H, 4.1O(1H, 4.39(1H, 5.20(2H, 6.88(lH, 6.96(1H, 7.03-7.22(7H, mn), 7.36(1H, 7.48-7.57(3H, in), 7.66(1H, 7.80(1H, 7.90(1H, 8.11(1H, br) FAB Mass(M+H) :579 Example Synthesis of 4 -{5-1 3 -(3-furan-2-ylmethyl-4-methyl-4-naphthalen-1 WO 99/05117 PCT/KR98/00225 dioxo-imidazolidin-1-yI)-propylJ-imidazol-1-ylmethyl}-benzonitrile(Compo und The title compound was prepared in a yield of 89% according to the same procedure as Example 1-1) to 1-2) except that hydroxy-propyl)-imidazol-l-ylmethyl]-benzonitrile was used instead of I-triphenylmethyl-imidazol-4-yl)-propanol in Example 1-1) and that 2-bromomethylfuran was used instead of ethyl bromoacetate in Example 1-2).
'H NMR(CDC1 3 8 (ppm) 1.78(3H, 2.07(2H, in), 2.48(2H, in), 3.76(3H, in), 4.58(1H, 5.16(2H, 5.84(1H, 6.08(lH, d), 7.03-7.22(6H, in), 7.32-7.52(5H, in), 7.65(1H, 7.90(2H, in), 8.23(1H, s) FAB Mass(M+H) :544 Example 56 Synthesis of {3-113-(fu ran-2-carbonyl)-4-methyl-4-naphthalen-1 -yI- 2,5-dioxo-imidazolidin-1-ylJ-propyl)-imidazol-I-ylmethyl)-benzonitrile (Compound 56) The title compound was prepared in a yield of 89% according to the same procedure as Example 1-1) to 1-2) except that hydroxy-propyl)-imnidazol-l-ylmethyl]-benzonitile was used instead of -triphenyln ethyl-iniidazol-4-yl)-propanol in Example 1-I) and that 2-fuiroyl chloride was used instead of ethyl bromoacetate in Example 1-2).
1 H NMR(CDCl 3 8'(ppm) 1.32(3H, 1.89(3H, 2.07(2H, in), 2.51(2H, in), 3.76(2H-, in), 4.06(lH, 4.26(2H, 4.43(lH, d), WO 99/05117 WO 9905117PCT/KR98/00225 86 5.96(1H, 6.73(1H, 7.10-7.22(5H, mn), 7.38(lH, 7.50(3H, in), 7.67(1H, 7.84(1H, 7.88(1H, 8.80(IH, s) FAB Mass(M+H) :616 Example 57 Synthesis of 2-12-(3- {3-13-(4-cyano benzyl)-311-im idazol-4-ylJ-p m ethyl-5-naphthalen-I -yl-2,4-d ioxo-imidazolidin-1-yI)-acetylamino]-4-met hylsulfanyl-butyric acid methyl ester(Com pound 57) The title compound was prepared in a yield of 60% according to the same procedure as Example 1-1) to 1-3) except that hydroxy-propyl)-imidazol-1I-ytmethyl]-benzonitrile was used isedof 3 -triphenylmethyl-imidazol-4-yl)-propanol in Example 1-1).
FAB Mass(M+H) :667 Example 58 Synthesis of 2-12-(3- {3-[3-(4-cyanobenzyl)-3H-im idazol-4-ylJ-p m ethyl-5-naphthalen-l-yI-2,4-d joxo-im idazolid in-I -yl)-acetylaminol-4-met hylsulfanyl-butyric acid lithium salt (Compound 58) The same procedure as Example 1-1) to 1-3) was carried out except that 4-[5 -hydroxy-propyl)-imidazol- 1-ylmethyl]-benzonitile was used instead of 1-triphenylmethyl-imidazol-4-yl)-propanoI in Example and then the resulting product was treated according to the samne procedure as Example 2 to obtain the title compound in a yield of FAB Mass(M+H) :652 Example 59 WO 99/05117 WO 9905117PCT/KR98/00225 87 Synthesis of 4-15-(4-methyl-4-naphthalen-1 -yI-2,5-dioxo-im idazolidin-1 -yl m ethyl)-imidazol-1-ylmethyll-benzonitrile(Com pound 59) The title compound was prepared in a yield of 70% according to the same procedure as Example 1-1) except that imidazol-1I-ylmethyl)-benzonitrile prepared in Preparation 7 was used instead of 3 -triphenyhmethyl-imidazol-4-yl)-propanol in Example 1-1).
'H NMR(CDCl 3 a (ppm) 1.93(3H, *4.54(2H, 5.333(2H, dd), 7.00(3H, in), 7.25(2H, in), 7.40-7.55(6H, in), 7.83(2H-, m) FAB Mass(M+H) :434 Example Synthesis of 4-I5-(3-m ethyl-4-m ethyl-4-naphthalen-1-yl-2,5-dioxo-im idazolidin-1 -ylm ethyl)-imidazol-1 -ylmethylj-benzonitrile(Com pound The title compound was prepared in a yield of 62% according to the same procedure as Example 1-1) to 1-2) except that mnethyl -imidazol- I -yhnethyl)-benzonitrile was used instead of 1triphenylinethyl-imidazol-4-yl)-propanol in Example 1-1) and that methyl iodide was used instead of ethyl bromoacetate in Example 1-2).
1 HNMR(CDCl 3 8 (ppm) 1.92(3H, 2.58(3H, 4.65(2H, dd.), 5.44(2H, 6.97(1H, 7.09(3H, in), 7.39(lH, 7.42(lH, d), 7.48(1H, 7.56(3H, in), 7.64(1H, 7.87(2H, m) FAB Mass(M+H) :450 Example 61 Synthesis of 4-15-(3-etbyl-4-methyl-4-naphthalen-1 -yl-2,5-dioxo-im idazo lid in-1 -ylm ethyl)-im idazol-1I -ylm ethyll-b enzon itrile(Com pou nd 61) WO 99/05117 WO 9905117PCTIKR98/00225 88 The title compound was prepared in a yield of 72% according to the same procedure as Example 1-1) to 1-2) except that hydroxymethyl-imidazol-1-ylmethyl)-benzonitrile was used instead of 3 -triphenylmethyl-imidazol-4-yl)-propanol in Example 1-1) and that ethyl iodide was used instead of ethyl bromoacetate in Example 1-2).
1 NMR(CDC1 3 3 (ppm) 0.76(3H-, 1.92(3H, 3.06(2H, q), 4.63(2H, dd), 5.46(2H, dd), 6.93(1H, 7.09(3H, in), 7.39(2H, d), 7.46(1H, 7.54(3H, in), 7.64(1H, 7.85(2H, mn) FAB Mass(M+H) :464 Example 62 Synthesis of 13- [3-(4-cyan o-benzyl)-3H-im idazol-4-yIm ethylj-5-m ethyl- 5-naphthalen-1-y-2,4-dioxo-imidazolidin-1-yl)-acetic acid ethyl ester (Compound 62) The title compound was prepared in a yield of 77% according to the same procedure as Example 1-1) to 1-2) except that hydroxymethyl-imnidazol- 1-ylmnethyl)-benzonitrile was used instead of 3 -triphenylinethyl-imidazol-4-yl)-propanol in Example 1-1).
I HNMR(CDC 3 8 (ppm) 1.14(3H-, 1.62(2H, 1.98(3H, s), 4.04(2H, in), 4.70(2H, 5.46(2H, dd), 6.93(1H, 7.07(1H, t), 7.12(2H, 7.41(2H, in), 7.48(1H, 7.55(1H, 7.58(2H, 7.65(1H, 7.85(1H, 7.89(1H, d) FAB Mass(M+H) :522 Example 63 Synthesis of 4- {5-[3-(3-cyanobenzyl)-4-methyl-4-naphthalen-1 WO 99/05117 PTK9/02 PCT/KR98/00225 89 d ioxo-im idazolidin-1 -ylm ethyl]-im idazol1-1 -ylm ethyl)}-benzo nitrile(C om pou nd 63) The title compound was prepared in a yield of 74% according to the same procedure as Example to 1-2) except that hydroxymethyl-imidazol- I -ylmethyl)-benzonitrile was used instead of 1-triphenylmethyl-imidazol-4-yl)-propanol in Example 1-1) and that 3-bromomethylbenzonitrile was used instead of ethyl bromoacetate in Example 1-2).
1H NMR(CDCl 3 a (ppm) 1.90(3H, 4.25(2H, dd), 4.72(2H, dd), 5.55(2H, dd), 6.68(1H, 6.80(1H, 6.90-7.35(6H, in), 7.40-7.90(8H, in), 8.10(1H, s) FAB Mass(M+H) :551 Example 64 Synthesis of 3-(3-im idazol-1-yl-propyl)-1-(4-m ethoxy-benzoyl)-5-m ethyl- 5-naphthalen-1-yl-imidazolidin-2,4-dione(Compound 64) The title compound was prepared i a yield of 80% according to the same procedure as Example 1-1) to 1-2) except that 3-(iinidazol- I -yl)-propanol was used instead of 1-triphenylmethyl-imidazol-4-yl)propanol in Example 1-1) and that 4 -inethoxy-benzoyl chloride was used instead of ethyl bromoacetate i Example 1-2).
H NMR(CDCI 3 8 (ppm) 2.30(2H4, ra), 2.48(3H, .3.71l-3.90(5H, mn), 4.13(2H, 6.81(2H4, 7.03(1H, 7.12(1H, 7.44-7.57(514, in), 7.63(114, 7.79(1H, 7.88(2H, 7.94(114, d) FAB Mass(M+H) :483 WO 99/05117 P~K9102 PCT/KR98100225 90 Example Synthesis of 3-(3-im idazol-1-yl-propyl)-5-methyl-1-(morpho line-4-ca rbon aphth alen-1-yl-im id azolidi n-2,4-d ion e(Com po un d The title compound was prepared in a yield of 61% according to the same procedure as Example 1-1) to 1-2) except that 3-(imidazol- I -yl)-propanol was used instead of 1-triphenylmethyl-imidazol-4yl)-propanol in Example 1-1) and that morpholine-4-carbonyl chloride was used instead of ethyl bromoacetate in Example 1-2).
1H NMR(CDCl 3 8 (ppm) 2.30(2H, 2.44(3H, 3.07(4H, br), 3.26(2H, br), 3.36(2H, br), 3.80(2H, in), 4.15(2H, 7.08(1H, s), 7.15(1H, 7.3 l(1H, 7.39(1H, 7.47(1H, 7.54(1H, 7.86(2H, in), 7.94(2H, d) FAB Mass(M+H) :462 Example 66 Synthesis of 3 3 -imidazol-1-yl-propyl)-5-methyl-5-naphthalen-1 -yl-2,4dioxo-imidazolidin-1-carboxylic acid 3 -cyano-phenyl)-amide(Com pound 66) The title compound was prepared in a yield of 58% according to the same procedure as Example 1-1) to 1-2) except that 3-(imidazol- 1 -yl)-propanol was used instead of 3 -triphenylmethyl-imidazol-4yl)-propanol in Example 1-1) and that 3 -isocyanatobenzonitrile was used instead of ethyl bromoacetate in Example 1-2).
'H NMR(CDC1 3 8 (ppm) 2.35(5H, in), 3.84(2H, br), 4.20(2H, t), 7.1O(lH, 7.20(1H, 7.32(3H, in), 7.40-7.55(3H, in), 7.60(LH, t), 7.81(1H, 7.84-7.98(3H, 8.29(1H, 1O.21(1H, s) WO 99/05117 WO 9905117PCT[KR98/00225 91 FAB Mass(M+H) :493 Example 67 Synthesis of N-4caottrhdoya--y)2 -3iidazol-1-ylpropyl)-5-methyl-5-naphthalen-1-yl-2 ,4-dioxo-im idazolidin-1-yll-acetamid e(Compound 67) The title compound was prepared in a yield of 67% according to the same procedure as Example 1-1) to 1-3) except that 3-(iniidazol- 1 -yl)-propanol was used instead of 3 -triphenylmethyl-imidazol-4yl)-propanol in Example 1-1) and that 4-amino-tetrahydropyran-4carbonitrile was used instead of methionine methyl ester in Example 1-3).
IH NMR(CDCl 3 3 (ppm) 1.57(2H, 1.92-2.10O(5H, in), 2.30(2H, mn), 3.49-3.62(3H, in), 3.67-3.76(4H, mn), 4.13(1H, 4.21(2H, 7.14(lH, 7.22(1H, 7.36(1H, 7.43(1H, mn), 7.46(1H, t), 7.51(1H, 7.72(1H, 7.90(1H, 7.98(1H, br), 8.30(1H, s) FAB Mass(M+H) :515 Example 68 Synthesis of 3-{3-[3-(4-bromo-benzyl)-3H-imidazo-4-yIJ-propyl)-5-methyI-5-naphthalen-1-yl-imidazolidin-2,4-dione(Compound 68) The title compound was prepared in a yield of 78% according to the samne procedure as Example 1-1) except that 3-[3-(4-broinobenzyl)-3H-iinidazol-4-yl]-propanol was used instead of 3-(1-triphenyl methyl-irnidazol-4-yl)-propanol.
I H NMR(CDC1 3 8 (ppm) 1.86(2H, in), 1.93(3H, 2.28(2H, in), WO 99/05117 PCT/KR98/00225 -92 3.54(2H, 4.73(2H, 6.67(2H, 6.70(1H, 7.20-7.36(6H, i) 7.56(1H, 7.71(1H, 7.75(1H, 7.90(1H, 8.46(1H, s) FAB Mass(M+H) :517 Example 69 Synthesis of 3- {3-[3-(4-brom o-benzyl)-3H-im idazol-4-ylJ-propyl}-1 m ethyl-5-naphthalen-1-yl-im idazolidin-2,4-d ione(Com pound 69) The title compound was prepared in a yield of 70% according to the same procedure as Example 1-1) to 1-2) except that [3-(4-bromobenzyl)-3H-imidazol-4-yl]-propanol was used instead of I-triphenylmethyl-imidazol-4-yl)-propanol in Example 1-1) and that methyl iodide was used instead of ethyl bromoacetate in Example 1-2).
1'H NMR(CDCl 3 3 (ppm) 1.89(3H, 2.05(2H, in), 2.47(2H, in), 2.61(3H, 3.73(2H, 4.97(2H, in), 6.83(2H, 6.95(1H, 7.28(1H, 7.38(2H, 7.43(11j, 7.49(1H, 7.65(1H, 7.70(1H, s), 7.88(2H, 8.00(1H, s) FAB Mass(M+H) :531 Example Synthesis of {3-13-(4-bromo-benzyl)-311-im methyl-5-naphthalen-1-y-2,4-dioxo-imidazolidin-1-yl)-acetic acid ethyl ester(Compound The title compound was prepared in a yield of 60% according to the same procedure as Example 1-1) to 1-2) except that [3-(4-bromobenzyl)-3H-imidazol-4-ylI-propanol was used instead of 3-(1-triphenylinethyl-iinidazol-4-yl)-propanol in Example 1-1).
WO 99/05117 WO 9905117PCT/KR98/00225 93 'HI NMR(CDCI 3 a (ppm) 1.24(3H, 1.95-2.15(5H, in), 2.51l(2H, in), 3.68(2H, 4.1 1(4H, in), 5.23(2H, 6.43(1H, 6.98(2H, d), 7.38-7.55(5H, in), 7.65(lH, 7.86(1H, 7.91(2H, mn), 9.25(LH, s) FAB Mass(M+H) :603 Example 71 Synthesis of 3-[3-(3-im idazol-1-yl-propyl)-5-m ethyl-5-phenyl-2,4-dioxoimidazolidin-1-ylmethyl]-benzonitrile(Compound 71) The title compound was prepared in a yield of 53% according to the same procedure as Preparation 1 and Example 1-1) to 1-2) except that acetophenone was used intead of acetonaphthone in Preparation I and 3-(imnidazol-1-yl)-propanol was used instead of 3-(l-triphenylmethyl-imidazol-4-yl)-propanol in Example 1-1) and that 3-bromomethylbenzonitrile was used instead of ethyl bromoacetate in Example 1-2).
H NMR(CDCl 3 a (ppm) 1.67(3H, 2.20(2H, mn), 3.67(2H, t), 4.00(2H, 4.05(1H, 4.78(1H, 6.98(1H, 7.06(1H, 7.]8(2H, in,7.39(5H, mn), 7.46(1H, 7.53(2H, mn) FAB Mass(M+H) :414 Example 72 Synthesis of 4-15-(3-naphthalen-1 -yl-2,5-dioxo-imidazolid in-1-ylm ethyl)im, idazol-1-ylm ethyl]-benzonitrile(Com pound 72) O.053g(0.24 minol) of the compound prepared in Preparation 2, 0.05 lg(0.24 minol) of the compound prepared in Preparation 7 and 0.079g(0.30 mmol) of triphenyiphosphine were dissolved in l0ni Of tetrahydrofuran and 0.047M (0.30 inmol) of diethylazodicarboxylate was WO 99/05117 PCTIKR98/00225 94 added thereto. The solution was stirred for 24 hours and tetrahydrofuran was removed under reduced pressure. Column chromatography was performed on the residue using a solvent mixture of methanol and dichloromethanol(3 :97) as an eluent to obtain 0.081 g of the title compound(Yield 80%, MW 421.5).
H NMR(CDCI 3 6 (ppm) 4.3 1(2H, 4.64(2H, 5.57(1H, s), 7.22(2H, 7.39(2H, in), 7.47(1H, 7.54(2H, in), 7.61(2H, d), 7.66(2H, in), 7.87-7.93(2H, mn) FAB Mass 422 Example 73 Synthesis of 3- [3-(4-chlo ro-benzyl)-311-im idazol-4-ylm ethyl]-lI -naphth alen-1 -yl-im idazo lid in-2,4-d ion e(Com pound 73) 73-1) Synthesis of 1-(4-chlorobenzyl)-5-hydroxymethyl-imidazole The title compound was prepared according to the same procedure as Preparation 6 except that 4-chlorobenzylamine was used instead of 4-bromobenzylamine in 54% yield.
H NMR(CDCl 3 8 (ppm) 2.78(LH, br), 4.49(2H, 5.20(2H, s), 6.93(1H, 7.07(2H, 7.32(2H, 7.45(1H, s) FAB Mass 223 73-2) Synthesis of 3 -(4-chloro-benzyl)-3H-imnidazol-4-ylmethyl]- 1naphthalen- 1-yl-imidazolidin-2,4-dione 0.07g(Yield 85%, MW 430.9) of the title compound was prepared using 0.046g(0.21 nimol) of the compound prepared in Example 73-1) and 0.043g(0. 19 minol) of the compound prepared in Preparation 2 according to the same procedure as Example 72.
41 WO 99/05117 PCT/KR98/00225 95 'H NMR(CDC1 3 3s (ppm) 4.16(2H1, 4.62(2H, 5.31(2H1, s), 7.22(2H, 7.39(2H, in), 7.47(1H, 7.54(2H, in), 7.6 1(2H1, d), 7.66(2H, mn), 7.87-7.93(2H, m) FAB Mass 431 Example 74 Synthesis of 4-r5-(3-naphthalen-1 -yl-2,5-d ioxo-im idazolidin-1-ylm ethyl)im idazol- 1-ylm ethyl] -piperid in e-1I-carboxyl ic acid benzyl ester (Compound 74) O.07g(Yield 81%, MW 537.6) of the title compound was prepared using O.090g(O.23 mniol) of the compound prepared in Preparation 5 and O.035g(O. 16 nimol) of the compound prepared in Preparation 2 according to the same procedure as Example 72.
1 HNMR(CDC1 3 3 (ppm) 1.30(2H, br), 1.62(2H, br), 1.92(11, in), 2.72(2H, br), 4.05-4.29(4H, br), 4.40(lH, 4.80(1H, 5.09(1H, s), 7.28-7.38(611, mn), 7.45-7.59(4H1, mn), 7.72(111, in), 7.84-7.96(3H, m) FAB Mass 538 Example Synthesis of 4-15-(3-naphthalen-1 -ylmethyl-2,5-dioxo-imidazolidin-1-yl m ethyl)-im idazol-1-ylmethylJ-benzonitrile(Com pound 75-1) Synthesis of (naphthalen-1-ylmethyl-amino)-acetic acid ethyl ester The title compound was prepared according to the same procedure as Preparation except that 1-naphthyl methyl amine was used instead of 1-naplithylamine in 90% yield.
WO 99/05117 WO 9905117PCT/KR98/00225 96 'H NMR(CDCl 3 a (ppm) 1.29(3H, I .98(lH, br), 3.51l(2H, s), 4.22(2H, 4.26(2H, 7.43(LH, 7.46-7.52(2H, in), 7.55(lH, in), 7.78(1H, 7.86(1H, 8.23(1H, d) FAB Mass 244 75-2) Synthesis of 1-(naphthalen- l-ylmethyl)-i*midazolidin-2,4-dione The title compound was prepared using the compound prepared in Example 75-1), according to the same procedure as Preparation 2-2) in 92% yield.
I NMR(CDCl 3 a (ppm) 3.5 7(2H, 4.9 1(2H, 7.33(]H, d), 7.38(1H, 7.45-7.54(2H, in), 7.79(1H, 7.83(1H, 8.05(1H, d) FAB Mass 241 75-3) Synthesis of 4-[5-(3-naphthalen- 1-ylinethyl-2,5-dioxo-imidazolidin- 1ylinethyl)-imidazol- 1 -ylmethyl]-benzonitrile 0.077g of the title compound was prepared using O.050g(O.21 iniol) of the compound prepared in Example 75-2) and O.047g(O.22 inmol) of the compound prepared in Preparation 7 according to the same procedure as Example 72(Yield 84%, MW 435).
1 HNMR(CDCl 3 8s'(ppm) 3.34(2H, 4.5 1(2H, 4.89(2H, s), 5.41(2H, 7.02(2H, 7.27(1H, 7.32(1H, 7.43(3H, in), 7.48(1H, 7.54 (2H, in), 7.89(2H, in), 8.05(1H, d) FAB Mass 436 Example 76 Synthesis of 4-[5-(3-naphthalen-1-ylmethyl-2,5-dioxo-imidazolidin-1-yI m ethyl)-imidazol-1 -ylmethyl]-piperidine-1-carboxylic acid benzyl ester (Compound 76) WO 99/05117 WO 9905117PCT/KR98/00225 97 0. lOg of the title compound was prepared using O.050g(O.2 I mmol) of the compound prepared in Example 75-2) and 0.
07 2g(0.22 mmol) of the compound prepared in Preparation 5 according to the same procedure as Example 72(Yield 87%, MW 551).
IIH NMR(CDCl 3 8 (ppm) 1.24(2H, br), 1.75(3H, br), 2.71(2H, s), 3.57(2H, 3.99(2H, 4.22(lH, br), 4.64(2H, 4.99(2H, 5.12(2H, 7.17 (11H, 7.34-7.39(7H, in), 7.44(1H, 7.54(2H, in), 7.87(2H, in,8.07(1H, d) FAB Mass 552 Example 77 Synthesis of {1 -[3-(4-cyano-benzyl)-311-im idazol1-4-yl m ethyl]I-3-n aph thalIen -1 -ylm ethyl-2,5-d ioxo-i m idazoIid in-4-yi} -acetic acid ethyl ester (Compound 77) 1.58g(Yield 90%, M\W 521) of the title compound was prepared using 1.10~g(3.37 minol) of the compound prepared in Preparation 3 and 0.86g(4.06 nimol) of the compound prepared in Preparation 7 according to the same procedure as Example 72.
IIH NMR(CDC 3 8 (ppm) 1.0 1(3H, 2.61l(2H, in), 3.59(1H, in), 3.67(lH, mn), 3.80(LH, in), 4.55(2H, dd), 4.76(lH, 5.13(1H, d), 5.42(2H, dd), 7.11 (2H, 7.30(lH, 7.34(1H, 7.41(1H, in), 7.49-7.54(5H, in), 7.87(2H, in), 8.03(1H, m) FAB Mass 552 Example 78 Synthesis of 11 -[3-(4-cyan o-b enzyl)-311-im id azol1-4-ylrn ethyl]j-3-na phth a len-1 -ylm ethyl-2,5-d ioxo-im id azolidin-4-y I-acetic acid (Cornpound 78) WO 99/05117 PCT1KR98/00225 98 0.7g(1.34 mmol) of the compound prepared in Example 77 was dissolved in a solvent mixture of tetrahydrofuran, methanol and water(3:2: 0. 12g (2.68 mmol) of lithium hydroxide monohydrate was added thereto and the solution was stirred for 1 hour. The solvents were removed under reduced pressure to obtain 0.66g of the title compound(Yield 95%, MW 516).
FAB Mass 517 Example 79 Synthesis of {1-[3-(4-cyano-benzyl)-3H-im idazol-4-ylmethyll-3-naphtha- Ien-1-ylm ethyl-2,5-dioxo-im idazo lid in-(4S)-yl) -acetic acid methyl ester (Compound 79) 0.364g(Yield 78%, MW 507) of the title compound was prepared using .287g(0.920 mmol) of the compound prepared in Preparation 4 and 0.21 5g( 1.01 mmol) of the compound prepared in Preparation 7 according to the same procedure as Example 72.
H NMR(CDC1 3 6'(ppm) 2.46(LH, dd), 2.63(1H, dd), 3.19(3H, s), 3.60(lH, in), 4.52(2H, 4.90(2H, dd), 5.40(2H, dd), 7.09(2H, d), 7.25(1H, 7.30 (1H, 7.37(1H, 7.45-7.49(4H, in), 7.53(1H, s), 7.79-7.85(2H, in), 8.00 (1H, d) FAB Mass 508 Example Synthesis of rpholin-4-yl-2-oxo-ethyl)-3-naphthalen-1 -yI idazolidin-1 -ylmethyll-im idazol-1 -ylmethyl}-benzonitr ile(Compound WO099/05117 PTK9102 PCT/KR98/00225 99 0.073g(0.14 inmol) of the compound prepared in Example 78, 0.018n,e (0.21 mmol) of morpholine and O.038g(0.28 mmnol) of N-hydroxybenzotriazole were dissolved in l 0 nje of dimethylformamide.
0. 04g (0.21 mmol) of 1 -ethyl -3 -dimethiylaminopropyl)carbodiimide was added thereto. The solution was strirred for 2 hours and dimethylformamide was removed under reduced pressure. 2OD, of ethylacetate was added to the residue and the organic layer was washed with water and saturated sodium bicarbonate solution. Then, ethylacetate was removed under reduced pressure. Column chromatography was peiformed using a solvent mixture of methanol and dichlorom ethane(3 :97) as an eluent to obtain 0.061g of the title compound(Yield 78%, MW 62).
IH NMR(CDC1 3 8 (ppm) 2.36(2H, in), 2.55(1H, in), 2.7 l(1H, in), 2.86(1H, in), 3.14(1H, mn), 3.29(1H, in), 3.88(1H, 4.62(3H, in), 5.25(1H, 5.46 (2H, dd), 7.13(2H, 7.30(1H, 7.32(1H, d), 7.40(1H, 7.50-7.57(5H, in), 7.87(2H, 8.07 (1H, m) FAB Mass 563 Example 81 Synthesis of 4- t( 5 4 2 -morpholin-4-yI-2-oxo-ethyl)-3-naphthalen-1 -yI m ethyl-2,5-dioxo-im idazolidin-1 -ylmethyl]-imidazol-1-ylmethyl}-benzo nitr ile(Compound 81) The same procedure as Example 78 was carried out using 0.071g(0.14 minol) of the compound prepared in Example 79 and the resulting product was treated according to the same procedure as Example 80 to obtain 0.059g of the title compound(Yield 75%, MW 562).
WO 99/05117 WO 9905117PCT/KR98/00225 100 'H NMR(CDCl 3 a' (ppmn) 2.32(1H, dd), 2.43-2.55(2H, in), 2.70(1H, in), 2.79 (1H, in), 3.16(1H, in), 3.20-3.36(4H, in), 3.96(1IH, t), 4.60-4.70(3H, in), 5.27 (11H, 5.58(2H, dd), 7.29(2H, 7.35(IH. d), 7.39(1H, 7.42(LH, 7.52-7.55(2H, mn), 7.60(2H, 7.85(1H, d), 7.88(l1-, in), 8.06(1H, in), 8.28 (1H, s) FAB Mass 563 Example 82 Synthesis of 2-{1-13-(4-cyano-benzyl)-3H-im idazol-4-ylm ethylj-3-naphthalen-1 -ylm ethyl-2,5-d ioxo-imidazolidin-4-yI}-N-(2-(N,N-dimethylamino)ethyl)-acetamide(Compound 82) 0.060g(Yield 78%, MW 550) of the title compound was prepared using 0.073g(0. 14 inmol) of the compound prepared in Example 78 and 0.0 161n(0. 18 minol) of 2-(N,N-dunethylamino)ethylaine according to the same procedure as Example 3.05(11- 4.90(11- 7.29(11- 'H NMR(CDC13) 8 (ppm) 2.34-2.60(2H, mn), I, in), 3.20 (2H, in), 3.27(3H, 3.68(1H, t), I, 5.03(1H, 5.26(11H, 5.44(2H, dd), I, 7.36(lH, 7.42(11H, 7.48-7.53(5H, mn), 2.91( 1H, 4.57(2H, 7. 12(2H, 7.87(2H, dd), dn), 8.09(1 H, mn) FAB Mass 551 Example 83 Synthesis of 2- {1-13-(4-bromo-benzyl)-3H-im idazol-4-ylmethyll-3-naphthalIen- 1-yl methyl1-2,5-d ioxo-i mid azo lid in-4-yl} eth oxy-ethyl)-N-m ethy l-acetamide(Com pound 83) WO 99/05117 PCT/LKR98/00225 -101 83-1) Synthesis of 2- 1-[3 -(4-bromo-benzyl)-3 H-imidazol-4-ylmethyl]-3 naphthalen- I -ylmethyl-2, 5-dioxo-imidazolidin-4-yl -acetic acid The title compound was prepared using the compounds prepared in Preparations 6 and 3 according to the samne procedures as Examples 72 and 78 in 83% yield.
FAB Mass 547 83-2) Synthesis of 2- 1-[3 -(4-bromo-benzyl)-3 H-imidazol-4-ylmethyl]-3 naphthalen- 1-ylmethyl-2, 5-dioxo-imidazolidin-4-yl }-N-(2-methioxy-ethlyl)-N-m ethyl-ace tamide 0.045g(Yield 73%, MW 617) of the title compound was prepared using 0.055g(0.10 mmol) of the compound prepared in Example 83-1) and 0.01 lg(0. 12 mmol) of N-methyl-2-methoxyethylamine according to the same procedure as Example H NMR(CDCI 3 8 (ppm) 2.36(1.5H, 2.44(1H, in), 2.58(1.5H, 2.65 (0.5H, dd), 2.80(0.5H, in), 2.89(lH, mn), 3.00-3.14(1H, in), 3.16(1H, 3.21 (1.5H, 3.25(1.5H, in), 3.63(1H, mn), 3.84(0.5H, t), 4.65(2H, 4.74(1H, dd), 5.09(1H, dd), 5.37(2H, 6.98(2H, t), 7.32-7.55(8H, mn), 7.77-7.88(2H, in), 8.08(1H, in) FAB Mass 618 Example 84 Synthesis of 4 5 4 2 -(4-methyl-piperazin-1-y)-2-oxo.ethyl..3.
n aphthalen-1-ylmethyl-2,5-dioxo-im idazolid in-1-ylmethyl}-im idazol-1-ylm ethyl)-benzonitrile(Compound 84) The same procedure as Example 78 was carried out using 0. 14g(0.28 inmol) of the compound prepared in Example 79 and the WO 99/05117 WO 9905117PCT/KR98/00225 102 resulting product was reacted 'With 0.0 44 DIJ(0.
4 0 nimol) of N-methyl-piperazine accordig to the samne procedure as Example 80 to obtain 0.1 ig of the title compound(Yield 71%, MW 575.7).
1 NMR(CDC 3 8 (ppm) 2. 15(2H, br), 2.22(3H, 2.39(2H, in), 2.73(1H, br), 2.84(1H, br), 2.97(1H, br), 3.28(1H, br), 3.87(1H, t), 4.58(2H, 4.68 (lH, 5.17(1H, 5.44(2H, dd), 7.12(2H, d), 7.27(1H, 7.3 1(lH, 7.39(1H, 7.48-7.56(5H, in), 7.83(lH, d), 7.87(lH, in), 8.05(1H, mn) FAB Mass 576 Example Synthesis of (2S)-(2-{1-I3-(4-cyano-benzyI)-3ll-imidazol-4-ylmethyl]-3n aphtbalen-1 -ylm ethyl-2,5-dioxo-im id azo lidin-4-yl} -acetam ino)-4-m ethyl su Ifanyl-butyric acid methyl ester(Compound 0. 17g(Yield 84 MW 638) of the title compound was prepared using 0. 16g(0.3 1 mmol) of the compound prepared in Example 78 and 0.066g(0.35 inmol) of (L)-methionine methyl .ester hydrochloride according to the same procedure as Example 'H NMR(CDCl 3 a (ppmn) 1.80(1H, mn), 1.96(LH, in), 2.05(3H, d), 2.32(1H, in), 2.38(1H, 2.52(1H, in), 2.65(1H, in), 3.73(4H, in), 4.29-4.40(1H, mn), 4.55(2H, dd), 4.74(lH, in), 5.24(1H, 5.44(2H, in), 6.04(1H, 7.11(2H, 7.27(1H, 7.37(lH, 7.42(lH, t), 7.47-7.53(5H, mn), 7.87(2H, in), 8.06(1H, mn) FAB Mass 639 Example 86 Synthesis of 13(I yn-eny)3-miao--lmtyl WO 99/05117 PCT/KR98/00225 103 naphthalen-1-ylm ethyl-2,5-dioxo-im idazolidin-4-yl}-acetamino)-4-methyl sulfanyl-butyric acid(Compound 86) The title compound was prepared using the compound prepared in Example 85 according to the same procedure as Example 78 in yield.
FAB Mass 625 Example 87 Synthesis of 3-(3-imidazol-1-yl-propyl)-l-naphthalen-1-yl-imidazolidin- 2,4-dione(Compound 87) 0.13g(Yield 91%, MW 334) of the title compound was prepared using 0.10g(0.44 mmol) of the compound prepared in Preparation 2 and 0.055g(0.44 mmol) of the compound prepared in Preparation 8 according to the same procedure as Example 72.
'H NMR(CDCl 3 (ppm) 2.18(2H, 3.66(2H, 3.99(2H, t), 4.31(2H, 6.95(1H, 7.02(1H, 7.17(1H, 7.42(1H, 7.50(2H, 7.65 (1H, 7.85(1H, 7.92(2H, m) FAB Mass 335 As mentioned above, compounds according to the present invention have an inhibitory activity against farnesyl transferase. In order to determine such inhibitory activity of the compounds, following experiments were performed.
Experimental Example 1 Analysis of Ras farnesyl transferase inhibiting activity W r OO/I 117 PCT/KR98/00225 104 In the present experiment, Ras farnesyl transferase produced by genetic recombination techniques by the improved Pompliano's method(Pompliano et al.; Biochemistry, 1992, 31, 3800) was used, Ras substrate (Ras-CVLS) protein was used by purifying by the known method(Chung et al., Biochemicia et Biophysica Act, 1992, 278, 1129).
The enzyme reaction was performed in 5 0fgt of 50mM Sodium HEPES buffer solution containing 25mmol of potassium chloride, of magnesium chloride, 10mmol of DTT and 50 mol of zinc chloride.
mol of Ras substrate protein, 0.15 p mol of tritiumfarnesylpyrophosphate and 4.5nmol of farnesyl transferase were used.
More specifically, in the initial step, farnesyl transferase was added to the above buffer solution, reaction was maintained for minutes at 37*C and then the reaction was stopped by adding lj of ethanol solution containing IM HC1. The formed precipitates were adsorbed to GF/B filter using Hopper harvestor(Hopper 225V) for filter-binding, washed with ethanol, and then radioactivity of the dried filter was measured using LKB R counter. Enzyme titer was measured in the unsaturated state of substrate where the concentrations of Ras substrate protein and farnesyl transferase have quantitative relationship.
Enzyme inhibiting activity was measured using less than 5% of total reaction solution of the compound according to the present invention dissolved in dimethylsulfoxide(DMSO) solution as a reagent. Enzyme inhibiting activity was represented by percentage of the amount of the farnesyl incorporated with the reagent to that without the reagent. ICso of the reagent was defined as the concentration inhibiting the enzyme activity by WO 99/05117 PCT/KR98/00225 105 To evaluate the selective enzyme inhibiting activity of the compound according to the present invention, inhibiting activity on geranylgeranyl transferase was measured. Geranylgeranyl transferase was purified from bovine brain with the method modified from Schber's method(Schber et al., J. Biol. Chem. 1990, 265, 14701), and substantially the same experiment as that of famesyl transferase was performed using geranylgeranyl pyrophosphate and Ras-CVIL substrate protein under the similar condition to farnesyl transferase reaction.
Experimental Example 2 Analysis of intracellular Ras farnesyl transferase inhibiting activity In the present experiment, Rat2 cell line which expresses C-Harvey-Ras protein having transforming activity and Rat2 cell line(Korean patent application No. 97-14409) which is transformed with fused protein of H-Ras substituted with polybasic lysine domain at C-terminus of K-Ras were used. The experiment was performed by the modified Declue's method(Declue. J. E. et al., Cancer Research, 1991, 51, 712). Hereinafter, the experimental method will be described in more detail.
3 x 105 cells of transformed Rat2 fibroblast cell line were sprayed on 60mm cell cultivation dish and cultivated for 48 hours in a cell incubator at 3 7°C and after 50% or more of density was reached, it was treated with a reagent. The compound according to the present invention dissolved in dimethylsulfoxide(DMSO) was used as the reagent.
1% of dimethylsulfoxide was used in both control and experimental groups. After 4 hours from the treatment of the reagent, methionine labeled with 150 P Ci of radioactive isotope, 35 S per 1 m of medium, was added and after cultivating for 20 hours, the cells were washed with WO 99/05117 PCT/KR98/00225 106 physiological saline water. The cells were lysed using 1l of cool cell lysis buffer solution(50mM of Sodium Herpiss buffer solution containing of magnesium chloride, Immol of DTT, 1% NP 40, Immol of EDTA, Immol of PMSF, 2 p mol of leupeptin, 2 p mol of pepstatin A and 2 mol of antipain) and the supernatant was obtained by high-velocity centrifugation of 12,000g x 5 minutes. The amount of the labeled radioisotope of the supernatent was measured and standardized to obtain a quantitative result in immunoprecipitation reaction and then, Y13-259, monoclonal antiboby specifically binding to Ras protein(Furth, M. E. et al., J. Virol, 1982, 43, 294) was added and reacted for hours at 4°C. Protein A bound to goat anti-murine Immunoglobulin antibody-agarose suspension was added to the solution and reacted for I hour at 4 0 c and then, to remove unspecific binding product, immunoprecipitates were washed with buffer solution(50mM Tris chloride buffer solution containing 50mmol of sodium chloride, 0.5% of sodium dioxycolate, 0.5% of NP 40 and 0.1% of SDS). The precipitates were boiled in reagent buffer solution for electrophoresis and then, electrophoresis was performed using 13.5% of SDS polyacrylamide gel.
Atfer electrophoresis, the gel was fixed and dried. Then, the gel was exposed to X-ray film, developed and printed. From the result of the experiment, intensities of band of protein with and without farnesyl of Ras protein were measured, and the concentration of reagent inhibiting of farnesyl binding was defined as CIC50, an intracellular Ras famesyl transferase inhibiting activity.
For the compound according to the present invention, from the results of the experiment according to the above Experimental Examples 1 and 2, ICso was 50 p M or less and CIC 5 0 was 100 p M or less. The results are shown in the below table 2a to 2d.
WO 99/05117 WO 9905117PCT/KR98/00225 107 Table 2a Ftase GGtase Compound No. IC 5 o (nM) CIC 5 0 M) ICS 0 (a M) 1 500 1 2 0.8 5 3.4 3 2500 5 4 4.8 10 0.7 190000 10 6 61 7.3 7 180 <20 8 14 <20 9 15 >1 >50000 <20 11 >50000 <20 12 5500 <20 13 1.5 <20 14 1 <20 2 <20 16 2500 <20 17 1500 <20 18 600 <20 19 240 <20 300 <20 21 150 <20 22 1700 j <20 3000 <20 WO 99/05117 PCT/KR98/00225 108 Table 2b Ftase GGtase Compound No. IC 5 o (nM) CIC 50 (au M) IC50 M) 24 750 <20 720 <20 26 700 <20 27 210 <20 28 1100 <20 29 80 <20 725 <20 31 900 <20 32 92 <20 33 1300 <20 34 2100 <20 500 <20 36 1200 <20 37 350 <20 38 250 <20 39 200 <20 1400 <20 41 530 <20 42 1000 <20 43 5000 <20 j 44 8000 <20 5500 <20 46 55 <20 WO 99/05117 WO 9905117PCT/KR98/00225 109 Table 2c Ftase GGtase Compound No. IC 5 0 (nim) CIC 50 M) IC 50 (P M) 47 18 <20 48 40 <20 49 55 <20 55 <20 51 19 <20 52 19 <20 53 65 <20 54 50 <20 45 <20 56 80 <20 57 16 400 58 14 <20 59 440 <20 160 <20 61 160 <20 62 50 <20 63 50 <20 64 700 <20 4500 <20 66 200 <20 67 3600 <20 68 5000 <20 69 [300 <20 WO 99/05117 PCT/KR98/00225 110 Table 2d Ftase GGtase Compound No. IC 5 0 (nM) CIC 5 o M) IC5o (p M) 5000 <20 71 7000 <20 72 20 <10 73 800 <50 74 4000 >50 30 <10 76 5000 >50 77 50 <10 78 100 <20 79 40 <10 90 <10 81 110 <20 82 150 <20 83 1500 >50 84 120 <20 200 <50 86 50 <10 87 5000 >50 As can be seen from the above results((IC5o 50 f M, CIC 5 o 100/ the novel hydantoin derivative according to the present invention effectively inhibits the activity of farnesyl transferase in transfering farnesyl group of Ras protein. Thus, the compound of formula can be advantageously used as an anti-cancer agent.

Claims (15)

1. A hydantoin derivative represented by the following formula [Formula I] 0 R, R3 N YN, R 4 0 or pharmaceutically acceptable salt thereof in which R, and R 2 independently of one another represent hydrogen; lower alkyl; monocyclic or bicyclic aryl group which can be substituted by lower alkyl or halogen; heterocyclic group containing hetero atoms selected from a group consisting of nitrogen and sulfur as ring member; or a radical having the following formula: 0 D (wherein D represents alkoxy; hydroxy; amino acid residue; morpholine; thiomorpholine; piperazine, alkoxyalkylamine or aryloxyalkylamine each of which is substituted or unsubstituted by lower alkyl, and m is selected from 0 to 2), R3 represents amino acid residue; or a radical having the following formula, 1< >i WO 99/05117 PCT/KR98/00225 112 A A B N N N wherein A represents hydrogen; lower alkyl; aryl group which is substituted by substituents selected from a group consisting of halogen, cyano(CN), nitro(NO2), carboxy(COOH), amide, thioamide, SR and lower alkyl; heterocyclic group which is substituted by substituents selected from a group consisting of halogen, cyano, nitro, COOR, amide, thioamide, SR and lower alkyl and which comprises nitrogen or sulfur atom as ring member; lower alkyl substituted by the substituted aryl or heterocyclic group as mentioned above; or a radical having the following formula: N-E (in the definition for the substituent A, R represents hydrogen or lower alkyl, and E represents hydrogen or -F-G wherein F represents CH 2 C=O, SO02, and G represents hydrogen; lower alkyl substituted or unsubstituted by phenyl or biphenyl; lower alkoxy; phenyl; benzyl; benzyloxy; amine substituted or unsubstituted by lower alkyl, phenyl, benzyl, cycloalkyl or phenoxy alkyl), B and C independently of one another represent hydrogen, halogen or lower alkyl, n denotes an integer of 0 to 4, R4 represents hydrogen; aromatic group substituted or unsubstituted by WO 99/05117 PCT/KR98/00225 113 lower alkyl or halogen; bicyclic aromatic group; heteroaromatic group containing hetero atoms selected from a group consisting of nitrogen and sulfur as ring member; or a radical having the following formula: 0 n R X H/n O 0 NHR 6 0 NHR R0 0 j /(nNIIJ(R R7 R 8 X X-v X R6 0^ 0 4{OR9 wherein Rs represents aryl group substituted by lower alkoxy; or heterocyclic group containing hetero atoms selected from a group consisting of nitrogen, oxygen and sulfur as ring member, R6 represents hydrogen; lower alkyl; lower alkyl which is substituted by substituents selected from a group consisting of halogen, cyano, hydroxy, COOR, amide, thioamide, SR and SO 2 R; lower alkyl substituted by an aryl group which is substituted by substituents selected from a group consisting of halogen, cyano, COOR, amide, thioamide, SR, SO 2 R and lower alkyl; heterocyclic group containing hetero atoms selected from a group consisting of nitrogen and sulfur as ring member; heterocyclic group which is substituted by substituents selected from a group WO 99/05117 PCT/KR98/00225 114 consisting of halogen, cyano, COOR, amide, thioamide, SR, SO 2 R and lower alkyl and which contains hetero atoms selected from a group consisting of nitrogen and sulfur as ring member, wherein R represents lower alkyl, R 7 and R 8 independently of one another represent hydrogen, halogen, halogenoalkyl, cyano, amide, thioamide, alkoxy or phenoxy, or represent a radical having the following formula, n'R Io -N Z-Rio -N io wherein Z represents CH 2 CO, 0, S, SO 2 NR 9 NHSO 2 or NHCOO, Rio represents hydrogen, lower alkyl, halogenoalkyl, alkoxy, hydroxy, benzyloxycarbonyl or benzyl, R9 represents hydrogen or lower alkyl, or lower alkyl substituted by aromatic group, X represents CH 2 CO, 0, S or S02, and n denotes an integer of 0 to 4.
2. The compound of claim 1 wherein Ri represents hydrogen; monocyclic or bicyclic aryl group which can be substituted by lower alkyl or halogen; or a radical having the following formula: 0 SD (wherein D represents alkoxy; hydroxy; amino acid residue; morpholine; thiomorpholine; piperazine or alkoxyalkylamine each of which is substituted or unsubstituted by lower alkyl, and m is selected from 0 to 1), R2 represents hydrogen; lower alkyl; or a radical having the WO 99/05117 PCT/KR98/00225 115 following formula: 0 o (wherein D represents alkoxy; hydroxy; amino acid residue; morpholine; thiomorpholine; piperazine or alkoxyalkylamine each of which is substituted or unsubstituted by lower alkyl, and m is selected from 0 to 1), R 3 represents a radical having the following formula, A A N C N<- C wherein A represents hydrogen; aryl group which is substituted by substituents selected from a group consisting of halogen, cyano(CN), nitro(NO2), carboxy(COOH), amide, thioamide, SR and lower alkyl; or a radical having the following formula: N-E (in the definition for the substituent A, R represents hydrogen or lower alkyl, and E represents hydrogen or -F-G wherein F represents C=O, and G represents benzyloxy, lower alkoxy, or lower alkyl substituted or unsubstituted by phenyl), B and C independently of one another represent hydrogen, n denotes an integer of 1 to 3, R4 represents hydrogen; aromatic group substituted or unsubstituted by halogen; bicyclic aromatic group; heteroaromatic group containing hetero atoms selected from a group consisting of nitrogen and sulfur as ring member; or a radical having the following formula: vs WO 99/05117 PCT/KR98/00225 116 o 0 R N NH OR 9 n 0 R8 OR, X Xy R wherein Rs represents aryl group substituted by lower alkoxy; or heterocyclic group containing hetero atoms selected from a group consisting of nitrogen, oxygen and sulfur as ring member, R6 represents hydrogen; lower alkyl; lower alkyl which is substituted by substituents selected from a group consisting of halogen, cyano, hydroxy, COOR, amide, thioamide, SR and SO 2 R; lower alkyl substituted by an aryl group which is substituted by substituents selected from a group consisting of halogen, cyano, COOR, amide, thioamide, SR, SO 2 R and lower alkyl; or heterocyclic group containing hetero atoms selected from a group consisting of nitrogen and sulfur as ring member; heterocyclic group which is substituted by substituents selected from a group consisting of halogen, cyano, COOR, amide, thioamide, SR, SO 2 R and lower alkyl and which contains hetero atoms selected from a group consisting of nitrogen and sulfur as ring member, wherein R represents lower alkyl, R 7 and R 8 independently of one another represent hydrogen, halogen, halogenoalkyl, cyano or phenoxy, or represent a radical having the following formula, WO 99/05117 WO 9905117PCTJKR98/00225 117 nzRo -N Ro C-N Z- wherein Z represents 0, S, S02, NR 9 NHS0 2 or NHCOO, Rio represents hydrogen, lower alkyl, halogenoalkyl, alkoxy, hydroxy or benzyloxycarbonyl, R 9 represents hydrogen or lower alkyl, X represents 0, S or SO 2 and n denotes an integer of 1 to 3.
3. The compound of claim 2 which is selected from a group consisting of: H-iinidazol-4-yl)-propyl]-5-methyl-5-naphthalen-1I-yl-2,4-dioxo-I midazolidin- l-yl }-acetylanmo)-4-methylsulfanyl-butyric acid methyl ester, {3 H-imidazol-4-yl)-propyl]-5 -methyl-5-naphthalen- 1-yl-2,4-dioxo-i m idazolidin- l-yl }-acetylaino)-4-methylsulfanyl-butyric acid, 3 1H-imridazol-4-yl)-ethyl]-5-methyl-5-naphthalen- 1-yl-2,4-dioxo-im idazolidin- l-yl }-acetylamino)-4-methylsulfanyl-butyric acid methyl ester, 3 1H-imidazol-4-yl)-ethyl]-5-methyl-5-naphthalen- 1-yl-2,4-dioxo-im idazolidin- 1-yl }-acetylaminmo)-4-methylsulfanyl-butyfic acid, 2- H-imidazol-4-yl-methyl)-5-methyl-5 -naplithalen- 1-yl-2,4-dioxo-imid azolidin- 1-yl]-acetylamino)}-4-methylsulfanyl-butyric acid methyl ester, 2-1{2-[3 -(3H-imidazol-4-yl-methyl)-5-methyl-5 -naplithalen-1I-yl-2,4-dioxo-imid azoildin- 1-yl]-acetylamnino}-4-methylsulfanyl-butyric acid, {3 -[3-(4-cyano-benzyl)-imidazol-4-yl-methyl]-5-methyl-5 -naphthalen-1I-yI -2,4-dioxo-imidazolidin- 1-yl}-acetylam-ino)-4-methylsulfanyl-butyric acid methyl ester, {3 -(4-cyano-benzyl)-imidazol-4-yl-methyl] -5-methyl-5 -naphthalen- 1-yl -2 ,4-dioxo-imidazolidin- I -yI }-acetylamino)-4-methylsulfanyl-butyric acid, 2 {3 -(3H-imidazol-4-yl)-propyl]-5-methyl-5 -naphthalen- 1-yl-2,4-dioxo-i WO 99/05117 WO 9905117PCT/KR98/00225 118 midazolidin- l-yl }-acetylamino)-3-thiophen-2-yl-propionic acid, 3 H-imidazol-4-yl)-propyl]-5-methyl-5-naphthalen- l-yl-l -(2-oxo-2-tbiazo lidin-3 -yl-ethyl)-imidazolidmn-2,4-dione, 1 1,1 -dioxo-thiazolidin-3 H-iinidazol-4-yl)-propyl]-5-methyl-5-nap hthalen- 1-yl-imidazolidin-2,4-dione, 3 H-imidazol-4-yl)-propyl]-5-methyl- 1- {2 -[2-(2-methylsulfanyl-ethyl)-thi azolidin-3 -yl]-2-oxo-ethyl)}-5-naphthalen- 1-yl-iinidazolidin-2 ,4-dione, -(3H-imnidazol-4-yl)-propyl]-5-methyl-5-naphthialen- 1-yl-2,4-dioxo-i midazolidmn- Il-yl I -acetylamnino)-4-methylsulfonyl-butyric acid, 2- {2-[3-(3-imidazol- 1-yl-propyl)-5-methyl-5-naphthalen- 1-yl-2,4-dioxo-imidaz olidin- 1-yI] -acetylainino }-4-methylsulfanyl-butyric acid, 2- -(2-imidazol- 1-yl-ethyl)-5-methyl-5-naphthalen- 1-yl-2,4-dioxo-imidazo lidmn-1I-yl]-acetylamino)}-4-methylsulfanyl-butyric acid, 1 -benzyl-3 -(3-imidazol- 1-yl-propyl)-5-methyl-5 -naphthalen- 1-yl-imidazolidin- 2,4-dione, 1 -(pentafluoro-benzyl)-3 -unidazol- 1-yI-propyl)-5-methyl-5-naphthalen- i-yb- imidazolidin-2,4-dione, 1 -pyridyhnethyl)-3 -(3-inidazol- 1-yl-propyl)-5-methyl-5 -naphthalen- 1-yI-im idazolidin-2,4-dione, 1 -chloro-benzyl)-3 -(3-imnidazol- 1-yl-propyl)-5-methyl-5-naphthalen- 1-yl-imi dazolidin-2,4-dione, 1 -bromo-benzyl)-3-(3-inidazol- 1-yl-propyl)-5-methyl-5 -naphthalen- l-yl-imn idazolidmn-2,4-dione, 1 -(4-bromo-benzyl)-3 -imidazol- 1-yI-propyl)-5-methyl-5 -naphthalen- 1-yl-im idazolidin-2,4-dione, 1 -trifluoromethyl-benzyl)-3 -inidazol- 1-yl-propyl)-5-methyl-5-naphthalen -1I -yl-imidazolidin-2,4-dione, 1 -(3-trifluoromethoxy-benzyl)-3-(3-imidazol- I -yl-propyl)-5-methyl-5 -naphthal en- I -yl-imidazolidi-2,4-dione, 3 -imidazol- 1 -yl-propyl)-5-methyl-5-naphthalen- Il-yl-l -(4-phenoxy-benzyl)-i WO 99/05117 PCTf]KR98/00225 -119- midazolidin-2,4-diofle, 3 )-imidazol- 1 -yl-propyl)-5-methyl-5-naphthalefl- I1-yl-i -phenoxy-benzyl)-i midazolidin-2,4-diofle, 3 -imidazol- 1 -yl-propyl)- I -(4-methyisulfanyl-benzyi)-5-metliyl-5-flaphthalefl -1I -yi-imidazolidin-2,4-diofle, 3 -imidazol- 1 -yl-propyl)-5-methyl- 1 -(4-methylsulfanyhinethyl-belzyl)-5 -nap hthaien- 1 -yl-imidazolidin-2,4-diolC, 3 -imidazol- 1 -yl-propyl)-5-methyi- 1 -1 -yl-imidazolidin-2,4-diofle, -imidazol- 1 -yi-propyl)-5 -methyl-5-naphthalen- I -yl-2,4-dioxo-imidazoli din- I -ylmethylI-2-methysulfalyl-belzofltflle, -imidazol- 1-yl-propyl)-5-methyl-5-naphthaldl- 1 -yl-2,4-dioxo-iinidazolI din- I -ylmethyl]-2-methylsulfoflbefzofitflle, -imidazol- 1 -yl-propyl)-S -methyl-5-naphthalen- 1 -yl-2,4-dioxo-iinidazoli din-i -ylmethyl]-benzoflitrile, 3 -imnidazol- 1-yl-propyl)-5-methyl-5-flaphthaldl- 1 -yl-2,4-dioxo-iinidazolI din-i -ylmethyl]-benzonitrile,
4-[3 -(3-imidazol- 1-yl-propyl)-5-methyl-5-naphthaldl- 1 -yl-2,4-dioxo-imidazolI din-i1 -ylmethyll-benzorntrile, 1 -(4-aminomethy1-benzyl)- 3 3 -imidazol-1I-yl-propyl)-5-methyl-S -naphthalen- I -yI-imnidazolidin-2,4-diofle, N- -(3-imnidazol- 1-yl-propyl)-5-methyl-S -naphthalen- 1-yl-2,4-dioxo-imida zolidin- I -yhnethyl]-benzyl} -methanesulfonamide, N- {3 -[3-(3-imidazol- 1 -y-propy)-5-methyl-5-naphthalen- I-yl-2,4-dioxo-imida zoli din-i1 -yhnethyi] -benzyl I -methane sulfonamide, N- -imidazol- 1-yl-propyl)-5-methyl-S -naphthalen- 1-yI-2,4-dioxo-inida zolidin- I -ylinethyll-benzyl} -methanesulfonamide, 4-13 -(3-imidazol- 1 -yipropyI)-5-methyl-5-flaphthalel"1-yb2 ,4-dioxo-imidazolI din- -ylmethyl]-benzoic acid methyl ester, 4-[3 -imidazol- 1-yl-propyi)-5 -methyl-5-naphthalel- 1-yi-2,4-dioxo-imidazolI WO099/05117 PCTIKR98/00225 -120- din- 1-ylmethyl]-benzoic acid, -imidazol- 1-yl-propyl)-l1-[3 -(morpholine-4-carbony)-benzyl]-5-mehyl-5-n aplithalen- I -yl-iiidazolidi-2,4-dione, 4- -imidazol- 1 -yl-propyl)-5-methyl-5 -naphthalen- 1 -yl-2,4-dioxo-imidazoli din- I -ylniethyl]-N-(2-methoxy-ethyl)-benzamide, 4-[3 -imidazol- 1 -yl-propyl)-5 -methyl-5 -naphthalen- 1 -yl-2,4-dioxo-imidazoli din- I -ylmethyl]-N-(2-methoxy-ethyl)-N-methyl-benzamide, 4-1{4-[3 -imidazol- 1 -yl-propyl)-5-methyl-5-naphthalen- 1 -yi-2,4-dioxo-imidaz olidin- I-ylmethyl]-benzoyl)}-piperazine-l1-carboxylic acid benzyl ester, 3 -imidazol- 1 -yl-propyl)- 1 -3 -(thi omorpholine-4-carbonyl)-benzyl]-5 -mnethyl 1 -yl-imnidazolidin-2,4-dione, 4-1{5-[3 -(4-methyl-4-naphthalen- 1-yl-2,5-dioxo-imidazolidin- 1-yl)-propyl]-imi dazol- I -ylmethyl~benzonitrile, 4-1{5-[3 -methyl-4-methyl-4-naphthalen- 1-yl-2,5-dioxo-imidazolidin-1I-yl)-pr opyl]-imidazol-1 -yhnethyl}-benzonitrile, 4- -(3-ethyl-4-methyl-4-naphthalen- 1-yl-2,5-dioxo-imidazolidin- 1-yl)-prop yI] -imidazol- I1-ylm ethyl) benzonitrile, 4- -propyl-4-methyl-4-naphthalen- l-yl-2,5 -dioxo-imidazolidin- 1-yl)-pr opyl]-imidazol- I-ylmethyl~benzonitrile, -(3-butyl-4-methyl-4-naphthalen-1I-yl-2,5-dioxo-imidazolidin- 1-yl)-prop yl]-imidazol- 1-ylmethyllbenzonitrile, -(2-methoxy-ethoxymethyl)-4-methyl-4-naphthalen- l-yl-2, midazolidin- 1 -yl]-propyl I -imidazol- I -ylmethyl)-benzonitrile, (3 3 -J3 -(4-cyanobenzyl)-3H-imidazol-4-yl]-propyl I -5-methyl-5-naphthalen- I yl-2,4-dioxo-imidazolidn- 1-yl)-acetic acid ethyl ester, {3 -[3-(4-cyanobenzyl)-3H-imidazol-4-yl]-propyl} -5-methyl-5-naphthalen- 1- yl-2,4-dioxo-imidazolidin- 1-yl)-acetic acid, {3 -benzyl-4-methyl-4-naphthalen- 1-yl-2,5-dioxo-imidazolidin- 1-yl]-pr opyl }-imidazol- 1-yhnethyl)-benzonitrile, 3 -cyano-benzyl)-4-m ethyl-4-naphthalen- l-yl-2,5 -dioxo-imidazolidI WO 99/05117 WO 9905117PCT/KR98/00225 121 n- I -yl] -propyl)}-iniidazol- 1 -yhnethyl)-benzonitrile, 4- {5 -fiiran-2-ylinethyl-4-methyl-4-naphthalen- l-yl-2, n- I -yl)-propyl]-imidazol- I -ylm ethyl I -benzonitrile, 4-(5-1{3-[3-(furan-2-carbonyl)-4-methyl-4-naphthalen- I -yl-2, din- I -yl]-propyl -imidazol- 1 -ylinethyl)-benzonitrile, 3-[3 -(4-cyano-benzyl)-3 H-iinidazol-4-yl]-propyl -5-methyl-5 -naphtha len- I -yl-2,4-dioxo-imidazolidin- I -yl)-acetylamino]-4-methylsulfanyl-butyric acid methyl ester, 2 3-[3 -(4-cyano-benzyl)-3 H-imnidazol-4-yl]-propyl -5-methyl-5 -naphtha len-i -yl-2,4-dioxo-imidazolidin- 1 -yl)-acetylamino]-4-methylsulfanyl-butynic acid, 4-[5-(4-methyl-4-naphthalen- Il-yl-2,5 -dioxo-imidazolidin- I -ylmethyl)-imidazoi I -ylmethyl]-benzonitrile, -methyl-4-methyi-4-naphthalen- 1-yl-2,5-dioxo-imidazolidin- 1-ylmethyl) -imidazol- I -ylmethyl]-benzonitrile, -ethyl-4-methyl-4-naphthalen- I1-yl-2,5-dioxo-imidazolidin- 1 -yhtnethyl)-i midazol- I -yhnethyl]-benzonitrile, 3-[3-(4-cyano-benzyl)-3H-imidazol-4-yhnethyl]-5-methyi-5-naphthalen- l-yl- 2,4-dioxo-imidazolidn- 1 -yl)-acetic acid ethyl ester, 4- {5 -(3-cyanobenzyl)-4-methyl-4-naphthalen- l-yl-2, 5-dioxo-imidazolidin- i -yhnethyi]-imidazoi-1i-ylmethyl)}-benzonitrile, 3 -imidazol- 1-yl-propyl)- 1-(4-methoxy-benzoyl)-5-methyl-5-naphthalen- l-yl -unidazolidm-2,4-dione, 3 -nnidazol- I -yl-propyl)-5 -m ethyl- I -(morpholine-4-carbonyl)-5 -naphthalen- 1 -yl-imidazoiidin-2,4-dione, 3 -(3-imidazol- 1-yl-propyl)-5-methyi-5-naphthalen- 1-yl-2,4-dioxo-imidazolidin e-l1-carboxylic acid (3 -cyano-phenyl)-amide, N-(4-cyano-tetrahydropyran-4-yl)-2-[3 -(3-imnidazol- 1-yl-propyi)-5-methyl-5 -na phthalen- 1-yl-2,4-dioxo-imidazolidin- 1-yl]-acetamnide, 3-1{3-[3 -(4-bromo-benzyl)-3H--imidazol-4-yl] -propyl} -5-methyl-5-naphthalen- 1 WO 99/05117 WO 9905117PCTIKR98/00225 122 -yl-irnidazolidi-2 ,4-dione, 3- 3 -(4-bromo-benzyl)-3H-imnidazol-4-yl]-propyl) -1,5-dimethyl-5-naphthale n- I -yl-imidazolidin-2,4-dione, (3 -1{3 -(4-bromo-benzyl)-3H-imidazol-4-yI]-propy I -yl-2,4-dioxo-iinidazolidn- I -yI)-acetic acid ethyl ester, 3 I-imidazol- 1-yl-propyl)-5-methyl-5-phenyl-2,4-dioxo-imidazolidin- 1-ylm ethyl] -benzonitrile, 4- [5-(3-naphthalen- l-yl- 2
5-dioxo-imidazolidin- 1-ylmethyl)-imidazol- 1-yhneth yl]-benzonitrile, 3 -(4-chloro-benzyl)-3H-imidazol-4-yhnethyl]-l1-naphthalen- 1-yl-imnidazolidI n-2,4-dione, 4- -naphthalen- l-yl-2, 5-dioxo-imidazolidin-1I-yhmethyl)-iinidazol- 1-ylmeth yI]-piperidme-l1-carboxylic acid benzyl ester, 4-[5-(3-naphthalen- 1-ylinethyl-2,5-dioxo-imidazolidin- 1-ylmethyl)-iinidazol- 1- ylm ethyl] -benzonitrile, 4- [5-(3-naphthalen- 1-ylmethyl-2,5-dioxo-imidazolidin- 1-ylinethyl)-imidazol- 1- ylmethyl]-piperidine-l-carboxylic acid benzyl ester, S1 -[3-(4-cyano-benzyl)-3 H-imidazol-4-yhnethyl]-3 -naphthalen- 1-ylmethyl-2,5- dioxo-imidazolidim-4-yl -acetic acid ethyl ester, I-[3-(4-cyano-benzyl)-3 H-imidazol-4-ylmethyl]-3 -naphthalen- 1-ylniethyl-2,5 dioxo-imidazolidin-4-yl I -acetic acid, 1-[3 -(4-cyano-benzyl)-3H-imidazol-4-ylinethyl]-3 -naphthalen-1I-ylmethyl-2,5- dioxo-imidazolidmn-(4S)-yl}I-acetic acid methyl ester, 4- {5-[4-(2-morpholin-4-yl-2-oxo-ethyl)-3 -naphthalen- 1-yhnethyl-2, idazolidn- 1 -yhnethyl]-imidazol- 1-yhnethyl)}-benzonitrile, 4- S)-[4-(2-morpholin-4-yl-2-oxo-ethyl)-3 -naphthalen- 1-yhnethyl-2,5 -dioxo- imidazolidin- 1-ylmethyl]-imnidazol-1-yhnethyl}-benzonitrile, 2-t (1-[3-(4-cyano-benzyl)-3 H-imidazol-4-ylmethyl] -3-naphthalen- 1-ylmethyl-2, -dioxo-imnidazolidmn-4-yl }-N-(2-(N,N-dimethylamnino)-ethyl)-acetamnide, 2- {11-[3 -(4-bromo-benzyl)-3 H-imidazol-4-ytm ethyl] -3 -naphthalen- 1 -ylmethyl-2 .5-dioxo-imidazolidmn-4-yl }-N-(2-methoxy-ethyl)-N-methyl-acetamide, {4-[2-(4-methyl-piperazin- 1-yl)-2-oxo-ethyl]-3-naphthalen-1I-yhnethyl- 1-yhnethyl}-imidazol-1-ylinethyl)-benzonitrile, 123 1-[3-(4-cyano-benzyl)-3H-imidazol-4-ylmethyl]-3-naphthalen- 1 dioxo-imidazolidin-4-yl}-acetylamino)-4-methylsulfanyl-butyric acid methyl ester, 1-[3-(4-cyano-benzyl)-3H-imidazol-4-ylmethyl]-3-naphthalen-1-ylmethyl-2,5- dioxo-imidazolidin-4-yl}-acetylamino)-4-methylsulfanyl-butyric acid, and 3-(3 -imidazol-1-yl-propyl)-1-naphthalen-1-yl-imidazolidin-2,4-dione. 4. A process for preparing a hydantoin derivative of formula as defined in any one of claims 1 to 3 wherein 1) a compound represented by the following formula (II): [Formula II] O R, NH N R4 0 wherein RI, R 2 and R 4 are as defined in claim 1, is reacted under Mitsunobu reaction condition with an alcohol derivative represented by the following formula (III): [Formula III] R 3 OH wherein R 3 is as defined in claim 1, or 2) a compound represented by the following formula (IIa): [Formula IIa] S..0. 4 wherein R, and R 2 are defined as previously described, is reacted with the alcohol derivative of formula (III) under Mitsunobu reaction condition to produce a compound represented by the following formula (Ia): [Formula Ia] [R:\LIBFF]09131 speci.doc:njc 124 O R,1 R3 N NH 0 wherein RI, R 2 and R 3 are defined as previously described, then substituent R 4 is introduced into the resulting compound of formula (la) to produce a compound represented by the following formula (Ib): [Formula Ib] O R1 R3 N R41 o 0 wherein RI, R 2 and R 3 are defined as previously described and R 4 is the same as R 4 except that R 4 is not hydrogen. An anti-cancer composition comprising the compound of formula as S* 10 defined in any one of claims 1 to 3 or prepared by the process of claim 4 or a pharmaceutically acceptable salt thereof as an active ingredient together with a •pharmaceutically acceptable carrier.
6. A method for the treatment or prophylaxis of an anti-proliferative disease comprising administering to a patient in need of such treatment or prophylaxis a i5 therapeutically effective amount of a hydantoin derivative according to any one of claims 1 to 3, a hydantoin derivative prepared by the process of claim 4 or a composition according to claim
7. The method according to claim 6 wherein the anti-proliferative disease is resfenosis, Rheumatitis arthritis or cancer.
8. Use of a hydantoin derivative according to any one of claims 1 to 3 or prepared by the process of claim 4 in the manufacture of a medicament for the treatment or prophylaxis of an anti-proliferative disease.
9. The use according to claim 8 wherein the anti-proliferative disease is resfenosis, Rheumatitis arthritis or cancer. [R:\LIBFF]0913 speci.doc:njc 125 A hydantoin derivative according to any one of claims 1 to 3 or prepared by the process of claim 4 when used for the treatment or prophylaxis of an anti-proliferative disease.
11. A hydantoin derivative when used according to claim 10 wherein the anti- proliferative disease is resfenosis, Rheumatitis arthritis or cancer.
12. A hydantoin derivative, substantially as hereinbefore described with reference to any one of compounds 1 to 37 or any one of the examples.
13. A process for preparing a hydantoin derivative, substantially as hereinbefore described with reference to any one of the examples.
14. An anti cancer composition comprising the hydantoin derivative of claim 12 or prepared by the process of claim 13 as active ingredient together with a pharmaceutically acceptable carrier. A method for the treatment or prophylaxis of an anti-proliferative disease comprising administering to a patient in need of such treatment, a therapeutically effective amount of a hydantoin derivative according to claim 12, a hydantoin derivative prepared by the process of claim 13 or a composition according to claim 14.
16. Use of a hydantoin derivative according to claim 12 or prepared by the process of claim 13 in the manufacture of a medicament for the treatment or prophylaxis of an anti-proliferative disease. 20 17. A hydantoin derivative according to claim 12 or prepared by the process of claim 13 when used for the treatment or prophylaxis of an anti-proliferative disease.
18. A hydantoin derivative whenever prepared by the process of claim 4 or 13. Dated 24 November, 2000 o: L G Chemical Ltd. S• 25 Patent Attorneys for the Applicant/Nominated Person SPRUSON FERGUSON [R:\LIBFF]09131 speci.doc:njc
AU84647/98A 1997-07-26 1998-07-24 Hydantoin derivatives having an inhibitory activity for farnesyl transferase Ceased AU729341B2 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
KR1019970035333A KR19990012061A (en) 1997-07-26 1997-07-26 HYDENTOIN DERIVATIVES USEFUL AS PANESSyltransferase inhibitor
KR1997/35333 1997-07-26
PCT/KR1998/000225 WO1999005117A1 (en) 1997-07-26 1998-07-24 Hydantoin derivatives having an inhibitory activity for farnesyl transferase

Publications (2)

Publication Number Publication Date
AU8464798A AU8464798A (en) 1999-02-16
AU729341B2 true AU729341B2 (en) 2001-02-01

Family

ID=19515820

Family Applications (1)

Application Number Title Priority Date Filing Date
AU84647/98A Ceased AU729341B2 (en) 1997-07-26 1998-07-24 Hydantoin derivatives having an inhibitory activity for farnesyl transferase

Country Status (7)

Country Link
EP (1) EP1000036A1 (en)
JP (1) JP2001510829A (en)
KR (2) KR19990012061A (en)
AR (1) AR015412A1 (en)
AU (1) AU729341B2 (en)
WO (1) WO1999005117A1 (en)
ZA (1) ZA986623B (en)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1255737A4 (en) * 1999-09-06 2003-04-16 Lg Chem Investment Ltd Process for preparing a 1-substituted 5-hydroxymethyl imidazole
WO2003018135A1 (en) 2001-08-24 2003-03-06 Wyeth Holdings Corporation Method of using 5-(arylsulfonyl)-,5-(arylsulfinyl), and 5-(arylsulfanyl)-thiazolidine-2,4-diones for inhibition of farnesyl-protein transferase
WO2003018554A1 (en) 2001-08-24 2003-03-06 Wyeth Holdings Corporation 3-substituted-3-(substitutedsulfonyl or sulfanyl)pyrrolidine-2,5-diones useful for inhibition of farnesyl-protein transferase
WO2003018011A1 (en) 2001-08-24 2003-03-06 Wyeth Holdings Corporation 5-(substituted)-5-(substitutedsulfonyl or sulfanyl)thiazolidine-2,4-diones useful for inhibition of farnesyl-protein transferase
CN1671387A (en) * 2002-07-31 2005-09-21 欧洲凯尔特股份有限公司 Aryl substituted hydantoin compounds and their use as sodium channel blockers
US20060116366A1 (en) * 2002-12-04 2006-06-01 Parmee Emma R Spirocyclic ureas, compositions containing such compounds and methods of use
TW200621766A (en) * 2004-09-17 2006-07-01 Hoffmann La Roche Substituted hydantoins
US7612212B2 (en) * 2006-02-22 2009-11-03 Hoffmann-La Roche Inc. Substituted hydantoins
KR101147583B1 (en) 2007-08-16 2012-05-21 에프. 호프만-라 로슈 아게 Substituted hydantoins
US20110038924A1 (en) * 2007-10-29 2011-02-17 Goomer Randal S Osteoarthritis gene therapy
KR20100086503A (en) * 2007-12-20 2010-07-30 에프. 호프만-라 로슈 아게 Substituted hydantoins as mek kinase inhibitors
WO2014019092A1 (en) * 2012-08-01 2014-02-06 The Hospital For Sick Children Inhibitors of peptidyl arginine deiminase (pad) enzymes and uses thereof
ES2686353T3 (en) * 2013-12-31 2018-10-17 Ipsen Pharma S.A.S. New derivatives of imidazolidino-2,4-dione
KR101593205B1 (en) 2015-06-12 2016-02-11 김윤태 A grass window cleaning apparatus

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0219363A (en) * 1988-07-06 1990-01-23 Fujisawa Pharmaceut Co Ltd Imidazolidine derivative
DE4009506A1 (en) * 1990-03-24 1991-09-26 Hoechst Ag hydantoin
DE4126277A1 (en) * 1991-08-08 1993-02-11 Cassella Ag HYDANTO DERIVATIVES
JPH0931060A (en) * 1995-07-25 1997-02-04 Nissan Chem Ind Ltd Production of cyclic urea compound
JP3449084B2 (en) * 1995-12-25 2003-09-22 富士レビオ株式会社 Hydantoin derivatives

Also Published As

Publication number Publication date
AU8464798A (en) 1999-02-16
ZA986623B (en) 1999-01-26
WO1999005117A1 (en) 1999-02-04
KR19990014070A (en) 1999-02-25
KR19990012061A (en) 1999-02-25
JP2001510829A (en) 2001-08-07
EP1000036A1 (en) 2000-05-17
KR100384116B1 (en) 2003-08-30
AR015412A1 (en) 2001-05-02

Similar Documents

Publication Publication Date Title
EP1058683B1 (en) Farnesyl transferase inhibitors having a piperidine structure and process for preparation thereof
AU729341B2 (en) Hydantoin derivatives having an inhibitory activity for farnesyl transferase
US6518292B1 (en) Heterocyclic aromatic compounds usefuls as growth hormone secretagogues
KR101015073B1 (en) Cis-4,5-biaryl-2-heterocyclic-imidazolines as mdm2 inhibitors
US9409888B2 (en) Dimeric compounds
CZ300127B6 (en) Process for preparing retroviral protease inhibiting intermediates
CZ18194A3 (en) Five-membered heterocycles, processes of their preparations and medicaments in which they are comprised
SK8752003A3 (en) CXCR3 antagonists, pharmaceutical composition comprising same and use thereof
KR20080077655A (en) Pdf inhibitors
CZ306297A3 (en) Piperazine compounds and pharmaceutical compositions containing thereof
EP1432700A1 (en) Spiro-hydantoin compounds useful as anti-inflammatory agents
EP0649843B1 (en) Thiazoline derivative
US6525203B1 (en) Heterocyclic aromatic compounds useful as growth hormone secretagogues
US8518976B2 (en) Heteroaryl-substituted amides comprising a saturated linker group, and their use as pharmaceuticals
US6384061B1 (en) Hydantoin compounds and methods related thereto
US6511978B1 (en) Pyrrole derivatives useful for farnesyl transferase inhibitors and their preparations
KR100381214B1 (en) Imidazolidine-2,4-dione derivatives useful as anticancer agents and preparation method thereof
KR100388792B1 (en) Farnesyl transferase inhibitor having piperidine structure and method for manufacturing the same
MXPA98004734A (en) Retrovi protease inhibitor compounds
KR19990074164A (en) Pyridin-2-one derivatives useful as farnesyl transferase inhibitors

Legal Events

Date Code Title Description
FGA Letters patent sealed or granted (standard patent)
MK14 Patent ceased section 143(a) (annual fees not paid) or expired