NZ610143B2

NZ610143B2 - Hybrid molecules containing pharmacophores of fluconazole as antifungal agents and their preparation

Info

Publication number: NZ610143B2
Application number: NZ610143A
Authority: NZ
Inventors: Hanumant Bapurao Borate; Mohan Anand Chandavarkar; Subhash Prataprao Chavan; Ramkrishnan Ramachandran Iyer; Deepali Damodar Rao; Sangmeshwer Prabhakar Sawargave; Amit Chandrakant Tawte
Original assignee: Council Of Scientific & Industrial Research; Fdc Limited
Priority date: 2011-06-15
Filing date: 2012-04-04
Publication date: 2016-01-06

Abstract

Disclosed herein are antifungal compounds of general Formula 1, wherein the substituents are as defined in the specification, which contain fluconazole pharmacophore moieties coupled with other moieties including aryl enones and chalcones. Also disclosed are methods for preparing compounds of Formula 1 and pharmaceutical preparations containing compounds of Formula 1 for prevention and treatment of fungal infections. Examples of a compound of Formula 1 are: (E)-1-(4-(2-(2,4-Difluorophenyl)-2-hydroxy-3-(1H-1,2,4-triazol-1-yl)propoxy)phenyl)-3-phenylprop-2-en-1-one (E)-1-(4-(2-(2,4-Difluorophenyl)-2-hydroxy-3-(1H-1,2,4-triazol-1-yl)propoxy)pheny 1)-3-(4-methoxyphenyl)prop-2-en-1-one S-(+)-(E)-3-(4-chlorophenyl)-1-(4-(2-(2,4-difluorophenyl)-2-hydroxy-3-(1H-1,2,4-triazol-1-yl)propoxy)phenyl)prop-2-en-1-one a 1 and pharmaceutical preparations containing compounds of Formula 1 for prevention and treatment of fungal infections. Examples of a compound of Formula 1 are: (E)-1-(4-(2-(2,4-Difluorophenyl)-2-hydroxy-3-(1H-1,2,4-triazol-1-yl)propoxy)phenyl)-3-phenylprop-2-en-1-one (E)-1-(4-(2-(2,4-Difluorophenyl)-2-hydroxy-3-(1H-1,2,4-triazol-1-yl)propoxy)pheny 1)-3-(4-methoxyphenyl)prop-2-en-1-one S-(+)-(E)-3-(4-chlorophenyl)-1-(4-(2-(2,4-difluorophenyl)-2-hydroxy-3-(1H-1,2,4-triazol-1-yl)propoxy)phenyl)prop-2-en-1-one

Description

GNA 1312 WO 1 “HYBRID MOLECULES CONTAINING PHARMACOPHORES OF FLUCONAZOLE AS ANTIFUNGAL AGENTS AND THEIR PREPARATION” TECHNICAL FIELD: The present invention discloses novel antifungal compounds of Formula 1, containing fluconazole pharmacophore moieties coupled with other moieties including aryl enones and chalcones and pharmaceutically acceptable salts thereof, methods for preparing these compounds and pharmaceutical preparations containing these novel compounds for prevention and treatment of fungal infections. 1 1 1 R A -B -C Formula 1 BACKGROUND AND PRIOR ART: The azole group of antifungal agents constitutes an important class of compounds useful in the treatment of various fungal infections. Fluconazole is one of the most important members of the family of azole antifungals as it is orally active and has low toxicity, but its extensive use has resulted in emergence of fluconazole-resistant fungal strains. This has made it necessary to develop analogues of fluconazole effective against resistant strains, and many new compounds have been reported. However, the issues like toxicity, solubility, cost, broad spectrum of activity, etc, make it inevitable to develop superior antifungal agents. The structure-activity relationship studies in case of fluconazole have shown that presence of one triazole ring, halogenated phenyl ring and tertiary alcoholic oxygen functionality is necessary for activity.

Some of the recent references describing synthesis and antifungal activity of fluconazole analogues are described in the following articles: Chemistry and Biodiversity 4, 1472 (2007); Bioorg. Med. Chem.Lett.17(13), 3686 (2007); Bioorg.Med. Chem. 16, 7055 (2008); Bioorg. Med. Chem. Lett. 18, 3261 (2008); GNA 1312 WO 2 Bioorg.Med. Chem. Lett. 18, 6538 (2008);Bioorg.Med. Chem. Lett. 19, 2013(2009); and Bioorg. Med.Chem. Lett. 20, 722(2010).

The compounds described in the present invention are however new compounds, and there is no prior art available for preparation of these compounds. Thus, the present invention seeks to provide novel azoles containing fluconazole pharmacophores and their preparation as an effort to come up with antifungal agents with superior antifungal activity.

SUMMARY OF THE INVENTION: Accordingly, the present invention discloses novel fluconazole analogues of Formula 1 containing fluconazole pharmacophores, which are useful as antifungal compounds.

In an aspect, the invention provides novel antifungal compounds of Formula 1, 1 1 1 R A -B -C Formula 1 wherein, X and Y may be same or different, and each represents hydrogen or halogen selected from fluorine, chlorine or bromine; Z is hydrogen, optionally substituted alkyl containing 1 to 5 carbon atoms, optionally substituted allyl, -COCH or optionally substituted phenyl; 1 2 3 4 R , R , R and R may be same or different, and each represents hydrogen or functional groups selected from alkyl group of linear or branched chain of 1 to 20 carbon atoms optionally substituted with phenyl group, alkoxy (-OR) group (wherein R= alkyl group GNA 1312 WO 3 with 1 to 4 carbon atoms), hydroxyl group, halogen selected from fluorine, chlorine, bromine or iodine, or nitro group; A and B are different, and represent –C=O, -CH=CH-, optionally substituted alkyl group of linear or branched chain of 1 to 20 carbon atoms, aziridinyl, epoxy ring, - CH(OR ) wherein R is H, alkyl group with 1 to 4 carbon atoms, acyl or phenyl, -C=N- 6 6 7 7 OR wherein R is H ormethyl, -C=N-R wherein R is alkyl group of linear or branched chain of 1 to 20 carbon atoms or phenyl, -C(X’R )Y’R wherein X’ and Y’ may be same or different and each represents -O or –S, and R and R represents alkyl group with 1 to 4 carbon atoms or phenyl or R and R are linked with each other to form a (hetero)cyclic five to eight-membered ring; or A and B together represent heterocyclic ring selected from 3,5-disubstituted (1H)-pyrazole or 3,5-disubstituted 4,5-dihydro(1H)-pyrazole; C represents hydrogen, optionally substituted phenyl, optionally substituted pyridyl, optionally substituted thienyl, optionally substituted naphthyl, optionally substituted anthracenyl, optionally substituted indolyl, optionally substituted cycloalkyl or optionally substituted alkyl group of linear or branched chain of 1 to 20 carbon atoms. ‘*’ is used to designate R or S configuration at carbon atom or racemic nature of the compound.

The present invention further relates to a process for preparation of antifungal compounds of Formula 1, and pharmaceutical preparations containing the antifungal compounds of Formula 1 for prevention and treatment of fungal infections.

DETAILED DESCRIPTION: The invention will now be described in detail in connection with certain preferred and optional embodiments, so that various aspects thereof may be more fully understood and appreciated.

Accordingly, the present invention provides novel antifungal compounds of Formula 1, containing fluconazole pharmacophore moieties and pharmaceutically acceptable salts GNA 1312 WO 4 thereof, methods for preparing these compounds and pharmaceutical preparations containing these novel compounds for prevention and treatment of fungal infections.

The compound of Formula 1 of the present invention is represented as follows; 1 1 1 R A -B -C Formula 1 wherein, X and Y may be same or different, and each represents hydrogen or halogen selected from fluorine, chlorine or bromine; Z is hydrogen, (un)substituted alkyl, (un)substituted alkenyl, (un)substituted acyl or (un)substituted aryl; 1 2 3 4 R , R , R and R may be same or different, and each represents hydrogen or functional groups selected from alkyl group of linear or branched chain of 1 to 20 carbon atoms optionally substituted with aryl group, alkoxy (-OR) group (wherein R= alkyl group with 1 to 4 carbon atoms), hydroxyl group, halogen selected from fluorine, chlorine, bromine and iodine, or nitro group; A and B are different, and represent –C=O, -CH=CH-, (un)substituted alkyl, cycloalkyl, 5 6 aziridinyl, epoxy ring, -CH(OR ) wherein R is H, alkyl, acyl or aryl, -C=N-OR wherein 6 7 7 8 9 R is H or alkyl, -C=N-R wherein R is alkyl or aryl, -C(X’R )Y’R wherein X’ and Y’ may be same or different and each represents -O or –S, and R and R represents alkyl or aryl or R and R are linked with each other to form a (hetero)cyclic five to eight- GNA 1312 WO 5 membered ring; or A and B together represent heterocyclic ring selected from 3,5- disubstituted (1H)-pyrazole or 3,5-disubstituted 4,5-dihydro(1H)-pyrazole; C represents hydrogen, (un)substituted (hetero)aryl, (un)substituted thienyl, (un)substituted naphthyl, (un)substituted anthracenyl, (un)substituted indolyl, (un)substituted cycloalkyl or (un)substituted alkyl; ‘*’ is used to designate R or S configuration at carbon atom or racemic nature of the compound.

In an embodiment, the present invention provides antifungal compounds of Formula 1, selected from; a) compounds of Formula 1A, with a proviso that A is –C=O when B is – CH=CH- ;or A is –CH=CH- when B is –C=O; b) compounds of Formula 1B, with a proviso that A is –C=O when B is (un)substituted alkyl, epoxy ring; or A is (un)substituted alkyl, epoxy ring when B is –C=O; c) compounds of Formula 1C, with a proviso that A is –CH=CH- when B is - 6 7 8 9 1 5 6 CH(OR ), -C=N-OR -C=N-R -C(X’R )Y’R , or A is-CH(OR ), -C=N-OR , , , 7 8 9 1 -C=N-R -C(X’R )Y’R when B is –CH=CH-, d) compounds of formula 1D where A and B together represent 3,5- disubstituted (1H)-pyrazole, e) compounds of formula 1E, where A and B together represent 3,5- disubstituted 4,5-dihydro(1H)-pyrazole, 1 2 3 4 5 6 7 8 9 1 wherein, ‘*’, X, Y, Z, R , R , R , R R , R , R , R R X’, Y’ and C are as , , , defined above.

In another embodiment, the invention provides a process for preparation of the compounds of Formula 1, as described above and which are distinguished in Table 1.

GNA 1312 WO 6 Table 1 Formula Z A B -H, (un)substituted alkyl, -C=O -CH=CH- (un)substituted alkenyl, (un)substituted acyl or -CH=CH -C=O (un)substituted aryl.

–C=O (un)substituted alkyl, -H, (un)substituted alkyl, (un)substituted alkenyl, epoxy ring (un)substituted acyl or (un)substituted –C=O (un)substituted aryl . alkyl, epoxy ring -CH(OR ), -CH=CH- -C=N-OR -H, (un)substituted alkyl, -C=N-R (un)substituted alkenyl, -C(X’R )Y’R (un)substituted acyl or -CH=CH- -CH(OR ), (un)substituted aryl . -C=N-OR -C=N-R -C(X’R )Y’R -H, (un)substituted alkyl, (un)substituted alkenyl, (un)substituted acyl or (un)substituted aryl -H, (un)substituted alkyl, (un)substituted alkenyl, (un)substituted acyl or (un)substituted aryl 1 2 3 4 5 6 7 8 9 1 X, Y, R , R , R , R R , R , R , R R X’, Y’ and C are as defined above.

, , , Preparation of compounds of formula 1A: The compounds of Formula 1A of the present invention are prepared by reacting an epoxide of Formula 2 with a compound of Formula 3 in presence of a base, with or without a phase transfer catalyst, to obtain corresponding compound of Formula 4, wherein the base is selected from potassium carbonate, sodium carbonate, cesium carbonate or lithium carbonate, and the phase transfer catalyst is selected from tetra-n- butylammonium bromide (TBAB), tetra-n-butylammonium chloride, benzyltriethylammonium bromide, benzyltriethylammonium chloride, cetyltri-n- butylphosphonium bromide, cetyltrimethylammonium bromide or cetyltrimethylammonium chloride. The compound of Formula 4 is further reacted with a GNA 1312 WO 7 suitable aldehyde/ketone in presence of a base selected from sodium hydroxide, potassium hydroxide, lithium hydroxide, sodium methoxide or potassium tert-butoxide, to obtain the compound of Formula 1A. The preparation of compound of Formula 1A is depicted in Scheme 1 as follows: Scheme 1: 1 2 3 4 5 6 7 8 9 wherein D represents -CHO or -COCH , and ‘*’,X, Y, R , R , R , R R , R , R , R R 3 , , , 1 1 1 X’, Y’, A , B and C are as defined above. The suitable aldehyde/ketone is selected from (un) substituted aliphatic/ aromatic/ heteroaromatic aldehyde or ketone.

The compounds of Formula 1A can also be obtained by reaction of an epoxide of Formula 2 with a substituted enone of Formula 5 in presence of a base, with or without phase transfer catalyst, wherein the base is selected from potassium carbonate, sodium carbonate, cesium carbonate or lithium carbonate, and the phase transfer catalyst is selected from tetra-n-butylammonium bromide (TBAB), tetra-n-butylammonium chloride, benzyltriethylammonium bromide, benzyltriethylammonium chloride, cetyltri-n- butylphosphonium bromide, cetyltrimethylammonium bromide or GNA 1312 WO 8 cetyltrimethylammonium chloride. The preparation of the compound of Formula 1A is depicted in Scheme 2 as follows: Scheme 2: The compounds of Formula 1A where Z is (un)substituted alkyl, (un)substituted alkenyl, (un)substituted acyl or (un)substituted aryl, are prepared by reacting the compounds of formula 1A (where Z is H) with halides of formula ‘ZX’ (wherein X is halogen selected from iodine, bromine or chlorine) via conversion of tertiary alcoholic group (-OH) to –OZ as depicted in Scheme 3 as follows: Scheme 3: GNA 1312 WO 9 Preparation of compound of Formula 1B: The compound of Formula 1B of the present invention is prepared by subjecting the compound of Formula 1A to various functional group transformations selected from halogenation, epoxidation or reduction of the unsaturated double bond(-CH=CH-) representing A or B in the compounds of Formula 1A.

Preparation of compound of Formula 1C: The compound of Formula 1C of the present invention is prepared by subjecting the compounds of Formula 1A to various functional group transformations selected from reduction, oximation or ketalization of the carbonyl group representing A or B in the compounds of Formula 1A.

Preparation of compound of Formula 1D: The compound of Formula 1D of the present invention is prepared by reacting compound of Formula 1B with hydrazine hydrate in presence of an acid selected from p-toluene sulfonic acid, acetic acid, propionic acid or trifluoroacetic acid.

Preparation of compound of Formula 1E: The compound of Formula 1E of the present invention is prepared by reacting compound of Formula 1A with hydrazine hydrate in presence of an acid selected from p-toluene sulfonic acid, acetic acid, propionic acid or trifluoroacetic acid.

Accordingly, the various compounds of Formula 1 prepared by aforementioned processes are mentioned in Table 2: Table 2: Compounds of Formula 1 1 1 1 1 2 3 4 Compoun A B C R R R R X Y Z d Nos. 1A-1 -CO- -CH=CH- Ph H H H H F F H -CO- -CH=CH- 4-methoxyphenyl H H H H F F H 1A-2 1A-3 -CO- -CH=CH- 2-methoxyphenyl H H H H F F H 1A-4 -CO- -CH=CH- 3,5- H H H H F F H dimethoxyphenyl 1A-5 -CO- -CH=CH- 3,4,5- H H H H F F H trimethoxyphenyl GNA 1312 WO 10 1A-6 -CO- -CH=CH- 4-chlorophenyl H H H H F F H 1A-7 -CO- -CH=CH- 2,4-dichlorophenyl H H H H F F H -CO- -H=CH- 2-fluorophenyl H H H H F F H 1A-8 1A-9 -CO- -CH=CH- 4-n- H H H H F F H octyloxyphenyl 1A-10 -CO- -CH=CH- 4-methoxyphenyl H H H H F H H 1A-11 -CO- -CH=CH- 4-methoxyphenyl H H H H Br H H 1A-12 -CO- -CH=CH- 4-chlorophenyl H H H H F H H 1A-13 -CO- -CH=CH- 2-thienyl H H H H F F H 1A-14 -CO- -CH=CH- 2-naphthyl H H H H F F H 1A-15 -CO- -CH=CH- 9-anthracenyl H H H H F F H 1A-16 -CO- -CH=CH- N-methyl H H H H F F H indolyl 1A-17 -CO- -CH=CH- 2-thienyl H H H H F H H 1A-18 -CO- -CH=CH- 2,4-dichlorophenyl H H H H F F allyl 1A-19 -CO- -CH=CH- 2,4-dichlorophenyl H H H H F F Me 1B-1 -CO- -CHBr- 2,4-dichlorophenyl H H H H F F H CHBr- 1C-1 - -CH=CH- 2,4-dichlorophenyl H H H H F F H CHOH- 1B-2 -CO- 2,4-dichlorophenyl H H H H F F H 1D-1 2,4-dichlorophenyl H H H H F F H 2,4-dichlorophenyl H H H H F F H 1E-1 -CH=CH- -CO- 4-methoxyphenyl H H H H F F H 1A-20 -CH=CH- -CO- 4-methylphenyl H H H H F F H 1A-21 1A-22 -CH=CH- -CO- 2,4-dichlorophenyl H H H H F F H 1A-23 -CH=CH- -CO- 4-methoxyphenyl OMe H H H F F H 1A-24 -CH=CH- -CO- 4-n- H H H H F F H octyloxyphenyl 1A-25 -CH=CH- -CO- methyl H H H H F F H GNA 1312 WO 11 1A-26 -CH=CH- -CO- n-pentyl H H H H F F H 1A-27 -CH=CH- -CO- n-tetradecyl H H H H F F H -CH=CH- -CO- cyclopropyl H H H H F F H 1A-28 1A-29 -CH=CH- -CO- H OMe H H H F F H The present invention provides pharmaceutical compositions comprising a therapeutically effective amount of compound of Formula 1 along with one or more suitable pharmaceutical carriers /exicipients.

The present invention relates to the use of the compound of Formula 1 for the treatment or prevention of fungal infections.

The present invention provides a method of treatment or prevention of a fungal infection to a subject by administering an effective amount of the compound of Formula 1 along with one or more suitable pharmaceutical carriers/exicipients. The dosage forms include solid dosage forms such as tablets, powders, capsules, liquid dosage forms as well as parenteral dosage forms. The dosage forms can also be prepared as sustained, controlled, modified and immediate release dosage forms. Active ingredient(s) and excipients can be formulated into compositions and dosage forms according to methods known in the art.

The invention is further illustrated with the following examples and should not be construed to limit the scope of the present invention. The features of the present invention will become more apparent from the following description of the inventive concept and the description of the preferred embodiments and appended claims.

GNA 1312 WO 12 Examples: Example 1: Procedure A: Preparation of (E)(2,4-dichlorophenyl)(4-(2-(2,4-difluorophenyl)- 2-hydroxy(1H-1,2,4-triazolyl)propoxy)phenyl)propenone (1A-7): (as per Scheme 1) O Cl Cl Step 1 To the flame dried K CO (1.45 g, 10.54 mmol), were added 1-(4- hydroxyphenyl)ethanone (4.21 mmol), tetra-butyl ammonium bromide (TBAB, 0.5 g) and 1-[2-(2,4-difluorophenyl)-oxiranylmethyl]-1H-[1,2,4]triazole(1.00 g, 4.21 mmol) dissolved in dry ethyl acetate (40 mL). The reaction mixture was allowed to stir under reflux for 12 h under nitrogen atmosphere. It was then cooled to room temperature, diluted with water, extracted with ethyl acetate, concentrated and purified by column chromatography to obtain 1-(4-(2-(2,4-difluorophenyl)hydroxy(1H-1,2,4-triazol yl)propoxy)phenyl)ethanone(Formula 4).

Step 2 To a solution of 1-(4-(2-(2,4-difluorophenyl)hydroxy(1H-1,2,4-triazol yl)propoxy)phenyl)ethanone (1.0 g, 2.68 mmol) of Formula 4 (obtained from Step 1) in methanol (20 ml), 2,4-dichlorobenzaldehyde (0.563 g, 3.21 mmol) was added. To this mixture, aq. sodium hydroxide (10%, 7.5 mL, 0.75 g, 13.5 mmol,) was added gradually while stirring. The mixture was stirred at room temperature for 18 h. It was then quenched with ice-cold water, the precipitate obtained was filtered and washed with water followed by aq. HCl (30%). It was then washed again with water, dried and recrystallized from methanol to get pure compound (E)(2,4-dichlorophenyl)(4-(2-(2,4- difluorophenyl)hydroxy(1H-1,2,4-triazolyl)propoxy)phenyl)propenoneof Formula 1A-7 as pale yellow solid (1.16 g, 82.3%). H NMR (200 MHz, CDCl ): δ 4.32 GNA 1312 WO 13 (s, 2H), 4.84 (s, 2H), 5.40 (bs, 1H), 6.72-6.90 (m, 4H), 7.18-7.42 (m, 3H), 7.54-7.75 (m, 3H), 7.87-8.02 (m, 3H).

Procedure B: Preparation of (E)(2,4-dichlorophenyl)(4-(2-(2,4-difluorophenyl)- 2-hydroxy(1H-1,2,4-triazolyl)propoxy)phenyl)propenone(1A-7): (as per scheme 2) To the flame dried K CO (1.45 g, 10.54 mmol), were added (E)(2,4-dichlorophenyl)- 1-(4-hydroxyphenyl)propenone (1.23 g, 4.21 mmol), tetra-butyl ammonium bromide (TBAB, 0.5 g) and 1-[2-(2,4-difluorophenyl)-oxiranylmethyl]-1H- [1,2,4]triazole(1.00 g, 4.21 mmol) dissolved in dry ethyl acetate (40 mL). The reaction mixture was allowed to stir under reflux for 12 h under nitrogen atmosphere. It was then cooled to room temperature, diluted with water, extracted with ethyl acetate, dried over Na SO , concentrated and purified by column chromatography using pet ether-ethyl acetate (40:60) as eluentto give pure compound (E)(2,4-dichlorophenyl)(4-(2-(2,4- difluorophenyl)hydroxy(1H-1,2,4-triazolyl)propoxy)phenyl)propenone of Formula 1A-7 as pale yellow solid (1.82 g, 81.6%).The H NMR spectrum was identical with the product obtained by procedure A.

Compounds of Formula 1A and chiral compounds thereof of Formula (R)-1A or (S)-1A can be prepared using procedure A or B.

GNA 1312 WO 14 The compounds prepared according to said procedures are depicted in Table 3 as follows: Table 3: Compoun Compounds Yield H NMR d No. % 1A-1 80.6 (200 MHz, CDCl ): δ 4.33 (s, 2H), 4.85 (s, 2H), 5.29 (bs, 1H), 6.73-6.95 (m, 4H), 7.16-7.39 (m, 4H), 7.48 (d, J= 16 Hz, 1H), 7.57-7.79 (m, (E)(4-(2-(2,4-Difluorophenyl)hydroxy- 4H), 7.96 (d, J= 8 Hz, 3-(1H-1,2,4-triazolyl)propoxy)phenyl) 2H), 8.06 (s, 1H) phenylpropenone 1A-2 83.4 (200 MHz, CDCl ): δ 3.85 (s, 3H), 4.33 (s, O OMe 2H), 4.89 (s, 2H), 6.76-7.03 (m, 6H), 7.39 (d, J= 16 Hz, 1H), 7.55-7.73 (m, E)(4-(2-(2,4-Difluorophenyl)hydroxy 3H), 7.81-7.88 (m, (1H-1,2,4-triazolyl)propoxy)phenyl)(4- 2H), 7.99 (d, J= 10 methoxyphenyl)propenone Hz, 2H), 8.06 (s, 1H) 81.3 200 MHz, CDCl ): δ 1A-3 3.89 (s, 3H), 4.25- 4.33 (m, 2H), 4.73 (bs, 1H), 4.84 (d, J= O MeO 14 Hz, 1H), 4.92 (d, J= 14 Hz, 1H), 6.75- 7.07 (m, 6H), 7.24 (d, J= 16 Hz, 1H), 7.43- 7.69 (m, 6H), 7.84 (s, 1H), 8.04 (s, 1H) (E)(4-(2-(2,4-Difluorophenyl)hydroxy- 3-(1H-1,2,4-triazolyl)propoxy)phenyl) (2-methoxyphenyl)propenone GNA 1312 WO 15 1A-4 79.7 (200 MHz, CDCl ): δ 3.82 (s, 6H), 4.32 (bs, 2H), 4.95 (bs, 2H), .43 (bs, 1H), 6.51 (s, 1H), 6.75-7.01 (m, 6H), 7.43 (d, J= 16 Hz, 1H), 7.58-7.72 (E)(4-(2-(2,4-Difluorophenyl)hydroxy- (m, 2H), 7.86-7.98 3-(1H-1,2,4-triazolyl)propoxy)phenyl) (m, 3H), 8.59 (s, 1H) (3,5-dimethoxyphenyl)propenone 1A-5 78.7 (200 MHz, CDCl ): δ 3.89 (s, 3H), 3.91 (s, 6H), 4.33 (s, 2H), 4.84 O OMe (bs, 1H), 4.88 (s, 2H), F OMe 6.75-6.96 (m, 6H), F 7.38 (d, J= 16 Hz, 1H), 7.58-7.74 (m, (E)(4-(2-(2,4-Difluorophenyl)hydroxy- 2H), 7.84 (s, 1H), 7.99 3-(1H-1,2,4-triazol- 1-yl)propoxy)phenyl) (d, J= 8 Hz, 2H), 8.04 (3,4,5-trimethoxyphenyl)propenone (s, 1H 1A-6 81.4 (200 MHz, CDCl ): δ 4.11 (bs, 2H), 4.65 O Cl (bs, 2H), 6.53-6.71 (m, 4H), 7.13 (d, J= 8 Hz, 2H), 7.23 (d, J= 16 Hz, 1H), 7.29-7.52 (m, 4H), 7.59 (s, 1H), (E)(4-Chlorophenyl)(4-(2-(2,4- 7.74 (d, J= 8 Hz, 2H), difluorophenyl)hydroxy(1H-1,2,4- 7.85 (s, 1H) triazolyl)propoxy)phenyl)propenone GNA 1312 WO 16 1A-7 82.3 (200 MHz, CDCl ): δ 4.32 (s, 2H), 4.84 (s, 2H), 5.40 (bs, 1H), 6.72-6.90 (m, 4H), O Cl Cl 7.18-7.42 (m, 3H), 7.54-7.75 (m, 3H), 7.87-8.02 (m, 3H).

(E)(2,4-Dichlorophenyl)(4-(2-(2,4- difluorophenyl)hydroxy(1H-1,2,4- triazolyl)propoxy)phenyl)propenone. 82.5 (200 MHz, CDCl ): δ 1A-8 4.33 (bs, 2H), 4.86 (bs, 2H), 6.73-6.83 (m, 2H), 6.89 (d, J= 8 N Hz, 2H), 7.04-7.19 (m, 2H), 7.29-7.40 (m, 1H), 7.54-7.68 (m, 3H), 7.80 (s, 1H), 7.85 (d, J= 16 Hz, 1H), 7.92 (d, J= 8 Hz, (E)(4-(2-(2,4-Difluorophenyl)hydroxy- 2H), 8.07 (s, 1H) 3-(1H-1,2,4-triazolyl)propoxy)phenyl) (2-fluorophenyl)propenone 1A-9 81.2 (200 MHz, CDCl ): δ H NMR (200 MHz, N CDCl ): δ 0.90 (t, J= O O-n-octyl 6 Hz, 3H), 1.26-1.50 (m, 10H), 1.74-1.87 (m, 2H), 4.00 (t, J= 8 Hz, 2H), 4.33 (bs, 2H), 4.71 (bs, 1H), (E)(4-(2-(2,4-Difluorophenyl)hydroxy- 4.82-4.98 (m, 2H), 3-(1H-1,2,4-triazolyl)propoxy)phenyl) 6.76-6.98 (m, 6H), (4-(octyloxy)phenyl)propenone 7.40 (d, J= 16 Hz, 1H), 7.57-7.71 (m, GNA 1312 WO 17 3H), 7.78 (d, J= 16 Hz, 1H), 7.86 (s, 1H), 7.99-8.04 (m, 3H) 1A-10 80.1 (200 MHz, CDCl ): δ 3.86 (s, 3H), 4.14 (d, O OMe J= 10 Hz, 1H), 4.21 (d, J= 10 Hz, 1H), 4.47 (bs, 1H), 4.62 (d, J= 14 Hz, 1H), 4.78 (d, J= 14 Hz, 1H), (E)(4-(2-(4-Fluorophenyl)hydroxy 6.91-6.98 (m, 4H), (1H-1,2,4-triazolyl)propoxy)phenyl)(4- 7.01-7.13 (m, 2H), methoxyphenyl)propenone 7.40 (d, J= 16 Hz, 1H), 7.49-7.64 (m, 4H), 7.78 (d, J= 16 Hz, 1H), 7.89-8.04 (m, 4H) 1A-11 79.3 (200 MHz, CDCl ): δ 3.86 (s, 3H), 4.11- 4.21 (m, 2H), 4.60 (d, O OMe J= 14 Hz, 1H), 4.64 (bs, 1H), 4.77 (d, J= 14 Hz, 1H), 6.90-6.96 (m, 4H), 7.34-7.53 (E)(4-(2-(4-Bromophenyl)hydroxy (m, 5H), 7.59 (d, J= 8 (1H-1,2,4-triazolyl)propoxy)phenyl)(4- Hz, 2H), 7.77 (d, J= methoxyphenyl)propenone 16 Hz, 1H), 7.91 (s, 1H), 7.99 (s, 1H), 8.00 (d, J= 8 Hz, 2H).

GNA 1312 WO 18 1A-12 79.2 (200 MHz, CDCl ): δ 4.14 (d, J= 10 Hz, O Cl 1H), 4.21 (d, J= 10 Hz, 1H), 4.50 (bs, 1H), 4.62 (d, J= 14 Hz, 1H), 4.78 (d, J= 14 Hz, 1H), 6.93-7.11 (E)(4-Chlorophenyl)(4-(2-(4- (m, 4H), 7.35-7.60 fluorophenyl)hydroxy(1H-1,2,4-triazol- (m, 7H), 7.75 (d, J= 1-yl)propoxy)phenyl)propenone 16 Hz, 1H), 7.89-8.03 (m, 4H). 1A-13 80.3 (200 MHz, CDCl ): δ 4.33 (bs, 2H), 4.87 (bs, 2H), 5.04 (bs, 1H), 6.75-6.94 (m, 4H), 7.04-7.11 (m, 1H), 7.25-7.42 (m, 3H), 7.57-7.70 (m, (E)(4-(2-(2,4-Difluorophenyl)hydroxy- 1H), 7.82 (s, 1H), 3-(1H-1,2,4-triazolyl)propoxy)phenyl) 7.87-7.98 (m, 3H), (thiophenyl)propenone 8.06 (s, 1H) 83.2 (200 MHz, CDCl ): δ 1A-14 4.28 (d, J= 8 Hz, 1H), 4.43 (d, J= 10 Hz, 1H), 5.01 (d, J= 14 Hz, 1H), 5.18 (d, J= 14 Hz, 1H), 6.79-6.88 (m, 2H), 6.96 (d, J= 8 (E)(4-(2-(2,4-Difluorophenyl)hydroxy- Hz, 2H), 7.44-7.55 3-(1H-1,2,4-triazolyl)propoxy)phenyl) (m, 4H), 7.57 (d, J= (naphthalenyl)propenone 16 Hz, 1H), 7.76-8.00 (m, 8H), 8.22 (s, 1H) GNA 1312 WO 19 1A-15 77.2 (200 MHz, CDCl ): δ 4.08-4.19 (m, 2H), 4.56 (bs, 1H), 4.72- 4.90 (m, 2H), 6.55 (d, J= 8 Hz, 2H), 6.74- 6.91 (m, 2H), 7.34- 7.63 (m, 8H), 7.83- (E)(Anthracenyl)(4-(2-(2,4- difluorophenyl)hydroxy(1H-1,2,4- 7.96 (m, 4H), 7.99 (s, triazolyl)propoxy)phenyl)propenone 1H), 8.03-8.12 (m, 2H), 8.31 (s, 1H) 80.7 (200 MHz, CDCl ): δ 1A-16 3.82 (s, 3H), 4.31- 4.39 (m, 2H), 4.81- 4.96 (m, 3H), 6.76- 6.88 (m, 2H), 6.95 (d, J= 10 Hz, 2H), 7.28- 7.39 (m, 4H), 7.44 (s, (E)(4-(2-(2,4-Difluorophenyl)hydroxy- 1H), 7.52 (d, J= 14 3-(1H-1,2,4-triazolyl)propoxy)phenyl) Hz, 1H), 7.59-7.71 (1-methyl-1H-indolyl)propenone (m, 1H), 7.85 (s, 1H), 7.96-8.10 (m, 4H) 1A-17 78.4 (200 MHz, CDCl ): δ 4.14 (d, J= 10 Hz, N 1H), 4.21 (d, J= 10 Hz, 1H), 4.62 (d, J= 14 Hz, 1H), 4.78 (d, J= 14 Hz, 1H), 6.93 (d, J= 10 Hz, 2H), (E)(4-(2-(4-Fluorophenyl)hydroxy 7.02-7.12 (m, 3H), (1H-1,2,4-triazolyl)propoxy)phenyl) 7.35-7.43 (m, 3H), (thiophenyl)propenone 7.47-7.57 (m, 2H), GNA 1312 WO 20 (E)(2,4-dichlorophenyl)(4-(2-(2,4- 7.88-8.03 (m, 5H). difluorophenyl)methoxy(1H-1,2,4- triazolyl)propoxy)phenyl)propenone. 1A-20 82.7 δ 3.89 (s, 3H), 4.25- 4.33 (m, 2H), 4.71 O OMe (bs, 1H), 4.81-4.96 (m, 2H), 6.76-7.00 (m, 6H), 7.43 (d, J= 16 Hz, 1H), 7.56-7.66 (m, 3H), 7.75 (d, J= (E)(4-(2-(2,4-Difluorophenyl)hydroxy- 16 Hz, 1H), 7.86 (s, 3-(1H-1,2,4-triazolyl)propoxy)phenyl) 1H), 8.00-8.05 (m, (4-methoxyphenyl)propenone 1A-21 83.4 (200 MHz, CDCl ): δ 2.43 (s, 3H), 4.24- Me 4.35 (m, 2H), 4.77 (s, 1H), 4.80-4.95 (m, 2H), 6.75-6.93 (m, 4H), 7.29 (d, J= 8 Hz, 2H), 7.41 (d, J= 16 (E)(4-(2-(2,4-Difluorophenyl)hydroxy- Hz, 1H), 7.54-7.66 3-(1H-1,2,4-triazolyl)propoxy)phenyl) (m, 3H), 7.75 (d, J= (p-tolyl)propenone 14 Hz, 1H), 7.84 (s, 1H), 7.92 (d, J= 8 Hz, 2H), 8.04 (s, 1H) 1A-22 81.1 (200 MHz, CDCl ): δ 4.27 (s, 2H), 4.82 (s, O Cl 2H), 5.22 (bs, 1H), 6.71-6.84 (m, 4H), 6.92 (d, J= 16 Hz, 1H), 7.25-7.46 (m, E)(2,4-Dichlorophenyl)(4-(2-(2,4- 6H), 7.53-7.62 (m, 1H), 7.75 (s, 1H), 8.04 GNA 1312 WO 21 difluorophenyl)hydroxy(1H-1,2,4- (s, 1H). triazolyl)propoxy)phenyl)propenone 1A-23 78.1 (500 MHz, CDCl ): δ 3.85 (s, 6H), 4.30 (d, OMe J= 8 Hz, 1H), 4.33 (d, F OMe J= 8 Hz, 1H), 4.83 (d, J= 12 Hz, 1H), 4.88 (d, J= 12 Hz, 1H), .11 (bs, 1H), 6.75- (E)(4-(2-(2,4-Difluorophenyl)hydroxy- 6.83 (m, 2H), 6.87 (d, 3-(1H-1,2,4-triazolyl)propoxy) J= 8 Hz, 1H), 6.95 (d, methoxyphenyl)(4-methoxyphenyl)prop J= 8 Hz, 2H), 7.10- enone 7.16 (m, 2H), 7.39 (d, J= 15 Hz, 1H), 7.56- 7.61 (m, 1H), 7.69 (d, J= 15 Hz, 1H), 7.77 (s, 1H), 8.00 (d, J= 8 Hz, 2H), 8.08 (s, 1H). 80.7 (200 MHz, CDCl ): δ 1A-24 0.89 (t, J= 6 Hz, 3H), N 1.28-1.51 (m, 10H), O-n-octyl 1.75-1.88 (m, 2H), 4.04 (t, J= 8 Hz, 2H), 4.25-4.35 (m, 2H), 4.72 (bs, 1H), 4.80- (E)(4-(2-(2,4-Difluorophenyl)hydroxy- 4.96 (m, 2H), 6.75- 3-(1H-1,2,4-triazolyl)propoxy)phenyl) 6.98 (m, 6H), 7.43 (d, (4-(octyloxy)phenyl)propenone J= 16 Hz, 1H), 7.55- 7.65 (m, 3H), 7.75 (d, J= 16 Hz, 1H), 7.85 (s, 1H), 7.99-8.04 (m, 3H).

GNA 1312 WO 22 1A-25 47.3 (200 MHz, CDCl ): δ 2.35 (s, 3H), 4.28 (s, 2H), 4.79-4.94 (m, 2H), 6.59 (d, J= 16 Hz, 1H), 6.74-6.89 (m, 5H), 7.40-7.48 (E)(4-(2-(2,4-Difluorophenyl)hydroxy- (m, 2H), 7.56-7.69 3-(1H-1,2,4-triazolyl)propoxy)phenyl)but- (m, 1H), 7.82 (s, 1H), 3-enone 8.04 (s, 1H). 1A-26 28.3 (200 MHz, CDCl ): δ 0.91 (t, J= 6 Hz, 3H), 1.22-1.38 (m, 4H), 1.60-1.71 (m, 2H), 2.63 (t, J= 8 Hz, 2H), 4.26-4.32 (m, 2H), 4.65 (s, 1H), 4.80- 4.96 (m, 2H), 6.63 (d, (E)(4-(2-(2,4-Difluorophenyl)hydroxy- J= 16 Hz, 1H), 6.78- 3-(1H-1,2,4-triazolyl)propoxy)phenyl)oct- 6.92 (m, 4H), 7.46- 1-enone: 7.54 (m, 3H), 7.57- 7.67 (m, 1H), 7.86 (s, 1H), 8.03 (s, 1H). 26.7 (400 MHz, CDCl ): δ 1A-27 0.87 (t, J= 6 Hz, 3H), n-tetradecyl 1.19-1.30 (m, 22H), N 1.61-1.66 (m, 2H), 2.61 (t, J= 6 Hz, 2H), 4.27 (s, 2H), 4.85 (s, 2H), 4.90 (bs, 1H), 6.63 (d, J= 16 Hz, (E)(4-(2-(2,4-Difluorophenyl)hydroxy- 1H), 6.77-6.87 (m, 3-(1H-1,2,4-triazol yl)propoxy)phenyl)heptadecenone 4H), 7.45-7.49 (m, 3H), 7.59-7.65 (m, GNA 1312 WO 23 1H), 7.81 (s, 1H), 8.04 (s, 1H). 1A-28 41.3 (200 MHz, CDCl ): δ cyclopropyl 0.91-1.03 (m, 2H), 1.11-1.19 (m, 2H), 2.16-2.26 (m, 1H), 4.23-4.33 (m, 2H), 4.71 (s, 1H), 4.80- 4.95 (m, 2H), 6.72- (E)Cyclopropyl(4-(2-(2,4- 6.92 (m, 5H), 7.50 (d, difluorophenyl)hydroxy(1H-1,2,4- J= 8 Hz, 2H), 7.57- triazolyl)propoxy)phenyl)propenone 7.69 (m, 2H), 7.85 (s, 1H), 8.04 (s, 1H). 1A-29 48.5 67 (m, 1H), 7.82 (s, 1H), 8.06 (s, 1H), 9.67 (d, J= 8 Hz, 1H).

(E)(4-(2-(2,4-Difluorophenyl)hydroxy- 3-(1H-1,2,4-triazolyl)propoxy) methoxyphenyl)acrylaldehyde Example 2: Preparation of 2,3-Dibromo(2,4-dichlorophenyl)(4-(2-(2,4-difluorophenyl) hydroxy(1H-1,2,4-triazolyl)propoxy)phenyl)propanone (1B-1): O Br O Cl Cl GNA 1312 WO 24 To a solution of (E)(2,4-dichlorophenyl)(4-(2-(2,4-difluorophenyl)hydroxy (1H-1,2,4-triazolyl)propoxy)phenyl)propenone (1A-7) (0.530 g, 1.0 mmol) in chloroform (10 ml), bromine (160 mg, 0.57 mL, 1.0 mmol) dissolved in chloroform (2 ml) was added slowly with stirring. After the completion of addition of bromine solution, the reaction mixture was stirred for 12 h. After completion of reaction, it was extracted with chloroform, dried over Na SO , concentrated and purified by column chromatography using pet ether-ethyl acetate (70:30) as eluent to give the pure product as 2,3-dibromo(2,4-dichlorophenyl)(4-(2-(2,4-difluorophenyl)hydroxy(1H-1,2,4- triazolyl)propoxy)phenyl)propanone of the Formula 1B-1 as off-white solid (561 mg, 81.1%). H NMR (200 MHz, CDCl ): δ 4.35 (bs, 2H), 4.84-4.99 (m, 2H), 5.14 (bs, 1H), 5.80 (bs, 1H), 6.15 (bs, 1H), 6.75-6.89 (m, 2H), 6.96 (d, J= 10 Hz, 2H), 7.33 (dd, J= 8, 2 Hz, 1H), 7.42 (d, J= 2 Hz, 1H), 7.52-7.68 (m, 2H), 7.86 (s, 1H), 8.03 (d, J= 10 Hz, 2H), 8.36 (s, 1H).

Example 3 Preparation of (3-(2,4-dichlorophenyl)oxiranyl)(4-(2-(2,4-difluorophenyl)hydroxy- 3-(1H-1,2,4-triazolyl)propoxy)phenyl)methanone (1B-2): O Cl Cl Powdered K CO (0.414 g, 3 mmol) was added to a solution of (E)(2,4- dichlorophenyl)(4-(2-(2,4-difluorophenyl)hydroxy(1H-1,2,4-triazol yl)propoxy)phenyl)propenone (Formula 1A-7) (0.530 g, 1.0 mmol) in MeOH (10 ml) at room temperature, followed by excess aqueous hydrogen peroxide (35%, 0.340 g, mmol); added over 10 min. The mixture was stirred at room temperature for 3 h and reaction progress was monitored by TLC (70:30 EtOAc/Pet ether). Upon completion, the MeOH was removed under reduced pressure and the resulting residue was extracted with CH Cl , dried over Na SO , concentrated and purified by column chromatography using 2 2 2 4 pet ether-ethyl acetate (60:40) as eluent to give the pure product (3-(2,4- GNA 1312 WO 25 dichlorophenyl)oxiranyl)(4-(2-(2,4-difluorophenyl)hydroxy(1H-1,2,4-triazol yl)propoxy)phenyl)methanone of Formula 1B-2 as pale yellow solid (482 mg, 88.4%). H NMR (200 MHz, CDCl ): δ 4.08 (d, J= 2 Hz, 1H), 4.29-4.33 (m, 3H), 4.80-4.96 (m, 3H), 6.75-6.91 (m, 2H), 6.95 (d, J= 10 Hz, 2H), 7.15-7.44 (m, 3H), 7.57-7.70 (m, 1H), 7.85 (s, 1H), 8.01 (d, J= 10 Hz, 2H), 8.04 (s, 1H).

Example 4 Preparation of (E)(2,4-dichlorophenyl)(4-(2-(2,4-difluorophenyl)hydroxy(1H- 1,2,4-triazolyl)propoxy)phenyl)propenol (1C-1): O Cl Cl To a solution of (E)(2,4-dichlorophenyl)(4-(2-(2,4-difluorophenyl)hydroxy (1H-1,2,4-triazolyl)propoxy)phenyl)propenone(Formula 1A-7) (500 mg, 0.943 mmol) in methanol (20 ml), was added sodium borohydride (35 mg, 0.943 mmol) at 0 C and allowed to stirr at room temperature for 3 h under nitrogen atmosphere. After completion of reaction, methanol was evaporated, extracted with ethyl acetate, dried over Na SO , concentrated and purified by column chromatography using pet ether-ethyl acetate (60:40) as eluent to give the pure product (E)(2,4-dichlorophenyl)(4-(2-(2,4- difluorophenyl)hydroxy(1H-1,2,4-triazolyl)propoxy)phenyl)propenol of Formula 1C-1 as white fluffy solid (437 mg, 87.3%). H NMR (200 MHz, CDCl ): δ 4.18-4.29 (m, 2H), 4.75 (bs, 1H), 4.83 (bs, 2H), 5.35 (d, J= 6 Hz, 1H), 6.33 (dd, J= 15, 6 Hz, 1H), 6.73-6.87 (m, 4H), 6.99 (d, J= 15 Hz, 1H), 7.15 (dd, J= 8, 2 Hz, 1H), 7.24-7.44 (m, 4H), 7.53-7.66 (m, 1H), 7.77 (s, 1H), 7.99 (s, 1H).

GNA 1312 WO 26 Example 5 Preparation of 1-(4-(5-(2,4-dichlorophenyl)-1H-pyrazolyl)phenoxy)(2,4- difluorophenyl)(1H-1,2,4-triazolyl)propanol (1D-1): The (3-(2,4-dichlorophenyl)oxiranyl)(4-(2-(2,4-difluorophenyl)hydroxy(1H- 1,2,4-triazolyl)propoxy)phenyl)methanone (1B-2) (546 mg, 1.0 mmol) was dissolved in xylene (10 mL) and p-toluenesulfonic acid (95 mg, 0.5 mmol) and hydrazine hydrate (150 mg, 3.0 mmol) were added to the epoxide solution. The reaction mixture was stirred under refluxing conditions for 3 h until a yellow precipitate formed. The xylene was removed under reduced pressure, extracted with ethyl acetate, dried over Na SO , concentrated and purified by column chromatography using pet ether-ethyl acetate (70:30) as eluent to yield the pyrazole compound 1-(4-(5-(2,4-dichlorophenyl)-1H- pyrazolyl)phenoxy)(2,4-difluorophenyl)(1H-1,2,4-triazolyl)propanol of Formula 1D-1 as pale yellow solid (467 mg, 85.7%).

H NMR (200 MHz, CDCl ): δ 4.19-4.30 (m, 2H), 4.87 (bs, 2H), 6.11 (bs, 2H), 6.76-6.90 (m, 5H), 7.16 (dd, J= 10, 2 Hz, 1H), 7.42 (d, J= 2 Hz, 1H), 7.52-7.75 (m, 4H), 7.85 (s, 1H), 8.02 (s, 1H).

GNA 1312 WO 27 Example 6 Preparation of 1-(4-(5-(2,4-dichlorophenyl)-4,5-dihydro-1H-pyrazolyl)phenoxy) (2,4-difluorophenyl)(1H-1,2,4-triazolyl)propanol (1E-1): A mixture of (E)(2,4-Dichlorophenyl)(4-(2-(2,4-difluorophenyl)hydroxy(1H- 1,2,4-triazolyl)propoxy)phenyl)propenone (1A-7) (500 mg, 0.943 mmol), hydrazine hydrate (1.17 g, 23.5 mmol) and acetic acid (10 mL) was heated at reflux for 4 h, then poured onto crushed ice. The precipitate obtained was separated by filtration, washed with water, and crystallized from methanol to give pure compound 1-(4-(5-(2,4- dichlorophenyl)-4,5-dihydro-1H-pyrazolyl)phenoxy)(2,4-difluorophenyl)(1H- 1,2,4-triazolyl)propanol of Formula 1E-1 as off-white solid (455 mg, 88.8%). H NMR (200 MHz, CDCl ): δ 2.94 (dd, J= 18, 4 Hz, 1H), 3.71 (dd, J= 18, 12 Hz, 1H), 4.27 (s, 2H), 4.83 (s, 2H), 5.74 (dd, J= 12, 4 Hz, 1H), 6.73-6.87 (m, 4H), 6.95 (d, J= 8 Hz, 1H), 7.14 (dd, J= 8, 2 Hz, 1H), 7.36 (d, J= 2 Hz, 1H), 7.53-7.65 (m, 3H), 7.79 (s, 1H), 8.08 (s, 1H).

Example 7 Preparation of (E)(2,4-dichlorophenyl)(4-(2-(2,4-difluorophenyl)methoxy(1H- 1,2,4-triazolyl)propoxy)phenyl)propenone (1A-19): O Cl Cl GNA 1312 WO 28 To a solution of (E)(2,4-dichlorophenyl)(4-(2-(2,4-difluorophenyl)hydroxy (1H-1,2,4-triazolyl)propoxy)phenyl)propenone (1A-7) (500 mg, 0.943 mmol) in dry DMF (20 ml), was added sodium hydride (37.7 mg, 0.943 mmol), followed by methyl iodide (0.10 mL, 1.69 mmol) at 0 C and allowed to stir at room temperature for 8 h under nitrogen atmosphere. The reaction was quenched with ice-cold water, extracted with ethyl acetate, dried over Na SO , concentrated and purified by column chromatography using pet ether-ethyl acetate (70:30) as eluent to give the pure product (E)(2,4- dichlorophenyl)(4-(2-(2,4-difluorophenyl)methoxy(1H-1,2,4-triazol yl)propoxy)phenyl)propenone of Formula 1A-19 as yellow fluffy solid (454 mg, 88.7%). H NMR (500 MHz, CDCl ): δ 3.34 (s, 3H), 4.45 (d, J= 10 Hz, 1H), 4.50 (d, J= Hz, 1H), 4.62 (d, J= 15 Hz, 1H), 4.73 (d, J= 15 Hz, 1H), 6.76-6.85 (m, 2H), 6.94 (d, J= 10 Hz, 2H), 7.20 (dd, J= 10, 2 Hz, 1H), 7.24-7.29 (m, 1H), 7.34 (d, J= 2 Hz, 1H), 7.41 (d, J= 15 Hz, 1H), 7.61 (d, J= 5 Hz, 1H), 7.73 (s, 1H), 7.95 (d, J= 10 Hz, 1H), 7.96 (s, 1H), 8.00 (d, J= 15 Hz, 1H).

Example 8 (E)(4-(2-(Allyloxy)(2,4-difluorophenyl)(1H-1,2,4-triazolyl)propoxy)phenyl)- 3-(2,4-dichlorophenyl)propenone (1A-18): O Cl Cl The same procedure described above for Formula 1A-19was used for the preparation of compound of Formula 1A-18 using allyl bromide instead of methyl iodide. Yield: 85.6%; H NMR (200 MHz, CDCl ): δ 4.09 (d, J= 4 Hz, 2H), 4.47 (dd, J= 10, 2 Hz, 1H), 4.61 (d, J= 10 Hz, 1H), 4.67 (d, J= 14 Hz, 1H), 4.81 (d, J= 14 Hz, 1H), 5.19-5.37 (m, 2H), 5.84- 6.03 (m, 1H), 6.81-6.96 (m, 2H), 6.99 (d, J= 8 Hz, 2H), 7.28-7.39 (m, 2H), 7.45 (d, J= 8 Hz, 1H), 7.49 (d, J= 7 Hz, 1H), 7.69 (d, J= 8 Hz, 1H), 7.82 (s, 1H), 8.03 (d, J= 8 Hz, 2H), 8.07 (s, 1H), 8.14 (s, 1H).

GNA 1312 WO 29 Example 9 Preparation of S-(+)- (E)(4-chlorophenyl)(4-(2-(2,4-difluorophenyl)hydroxy (1H-1,2,4-triazolyl)propoxy)phenyl)propenone (Formula S-(+)-1A-6): O Cl To the flame dried K CO (262 mg, 1.9 mmol), were added (E)(4-chlorophenyl)(4- hydroxyphenyl)propenone (232 mg, 0.91 mmol), tetra-butyl ammonium bromide (TBAB, 246 mg) and S-(-)[2-(2,4-difluorophenyl)-oxiranylmethyl]-1H-[1,2,4]triazole (180 mg, 0.76 mmol) dissolved in dry ethyl acetate (15 mL). The reaction mixture was allowed to stir under reflux for 12 h under nitrogen atmosphere. It was then cooled to room temperature, diluted with water, extracted with ethyl acetate, dried over Na SO , concentrated and purified by column chromatography using pet ether-ethyl acetate (40:60) as eluent to give pure compound of Formula S-(+)-1A-6 (240 mg, 64.3%). [α] + 11.91º (c=1, THF). Chiral HPLC using Chiralcel OD-H (250 x 4.6 mm) column using % ethanol in pet ether as mobile phase showed the product to have RT 31.817 min and 77.9% ee.

The following compounds given herein below in Table 4 were prepared using above procedure by reaction of various hydroxyl chalcones with suitable epoxides: GNA 1312 WO 30 Table 4 Compound Compounds [α] HPLC RT ee Nos. conditions (min) (%) R-(-)-1A-2 -11.28º Chiralcel OD-H 32.800 71.8 (250 x 4.6 mm), ethanol - pet O OMe N ether (25:75), 254 nm R-(-)-(E)(4-(2-(2,4- Difluorophenyl)hydroxy(1H- 1,2,4-triazolyl)propoxy)phenyl)- 3-(4-methoxyphenyl)propen S-(+)-1A-2 +13.80º Chiralcel OD-H 40.767 95.2 (250 x 4.6 mm), ethanol - pet O OMe N ether (25:75), 254 nm S-(+)-(E)(4-(2-(2,4- Difluorophenyl)hydroxy(1H- 1,2,4-triazolyl)propoxy)phenyl)- 3-(4-methoxyphenyl)propen +13.59º Chiralcel OD-H 28.317 94.7 S-(+)-1A- 13 (250 x 4.6 mm), iso-propanol - pet ether (40:60), 254 nm S-(+)-(E)(4-(2-(2,4- Difluorophenyl)hydroxy(1H- 1,2,4-triazolyl)propoxy)phenyl)- 3-(thiophenyl)propenone R-(-)-1A- -11.98º Chiralcel OD-H 41.567 94.2 13 (250 x 4.6 mm), iso-propanol - pet ether (40:60), 254 nm GNA 1312 WO 31 R-(-)-(E)(4-(2-(2,4- Difluorophenyl)hydroxy(1H- 1,2,4-triazolyl)propoxy)phenyl)- 3-(thiophenyl)propenone Example 10 Preparation of R-(-)- (E)(4-chlorophenyl)(4-(2-(2,4-difluorophenyl)hydroxy (1H-1,2,4-triazolyl)propoxy)phenyl)propenone (Formula R-(-)-1A-6): O Cl Racemic 1A-6 was resolved by preparative chiral HPLC using Chiralcel OD (16 x 100 mm) column and pet ether-ethanol (75:25) as eluent. The enantiomer that eluted out first was found to be R-(-)- (E)(4-chlorophenyl)(4-(2-(2,4-difluorophenyl)hydroxy (1H-1,2,4-triazolyl)propoxy)phenyl)propenone (Formula R-(-)-1A-6) with [α] - 12.30º (c=1.1, THF). Chiral HPLC using Chiralcel OD-H (250 x 4.6 mm) column using % ethanol in pet ether as mobile phase showed the product to have 97.8% ee.

Example 11 Antifungal Activity Testing: The compounds of Formula 1 were tested for antifungal activity against Candida albicans, AspergillusnigerandFusariumproliferatum. In vitro evaluation of antifungal activity was performed by determining the minimum inhibitory concentration (MIC) following standard methods (CLSI: Reference method for broth dilution antifungal susceptibility testing of yeasts; Approved standard, second edition M27-A2, 2002; CLSI: Reference method for broth dilution antifungal susceptibility testing of filamentous fungi; Approved standard M38-A, 2002). Anti-fungal susceptibility testing of these anti-fungal compounds was done by broth dilution method using RPMI 1640 medium with MOPS buffer. Known anti-fungal agents like fluconazole and amphotericin-B were used as positive control. End points were determined after 48 hours visually and by using GNA 1312 WO 32 spectrophotometer wherever necessary. Different dilutions were tried and various sets of experiments performed. The activity parameters are enumerated in Table5.

Table 5: Activity against organisms (MIC in μg/ml)* Sr Ca01 Ca01 Cg01 Ck01 Ct01 Cn01 An01 Afm Fp01 Comp no no A B 01 1 FLU 1 0.25 1 32 1 2 >128 >128 >128 2 AMB 0.25 0.25 0.25 0.5 0.5 0.5 0.25 0.5 2 1A-1 0.12 0.06 0.25 >2 0.5 1 >2 >2 >2 4 1A-2 0.12 0.06 0.25 4 0.25 1 4 >4 >4 1A-3 0.5 0.25 0.5 >8 2 8 >8 >8 >8 1A-4 1 0.25 2 >4 2 2 >4 >4 >4 7 1A-5 1 0.25 1 >4 1 >4 >4 >4 >4 8 1A-6 0.25 0.5 0.5 2 0.5 0.5 >4 >4 >4 9 1A-7 0.25 0.25 0.5 2 1 2 >4 >4 >4 1A-8 0.12 0.12 0.25 4 0.5 2 >4 >4 >4 11 1A-9 >2 >2 >2 >2 >2 >2 >2 >2 >2 12 1A-10 2 0.25 0.5 4 4 0.5 >4 >4 >4 1A-11 1 0.5 1 >4 >4 1 >4 >4 >4 14 1A-12 2 0.5 0.5 4 4 0.5 >4 >4 >4 1A-13 0.25 0.12 0.25 8 0.5 1 >8 >8 >8 1A-14 0.5 0.25 0.5 1 0.5 0.5 >4 >4 >4 17 1A-15 >2 >2 2 >2 >2 2 >2 >2 >2 18 1A-16 0.5 0.25 2 >4 2 4 >4 >4 >4 19 1A-17 0.5 0.25 0.25 8 2 1 >8 >8 >8 1A-18 >4 >4 >4 >4 >4 >4 >4 >4 >4 21 1A-19 >4 1 1 >4 >4 >4 >4 >4 >4 22 1B-1 0.5 0.25 0.5 2 1 0.5 >8 >8 >8 1C-1 0.5 0.5 0.25 4 1 0.5 >4 >4 >4 24 1B-2 0.5 0.5 0.5 4 1 1 >4 >4 >4 1D-1 0.5 0.5 1 2 0.5 1 >4 >4 >4 26 1E-1 0.25 0.25 2 >8 1 2 >8 >8 >8 27 1A-20 0.25 0.12 0.25 4 1 1 >4 8 >4 28 1A-21 0.25 0.12 0.25 2 1 1 >4 8 >4 29 1A-22 0.25 0.12 0.5 2 1 1 >4 >4 >4 1A-23 0.5 0.5 1 2 0.5 1 >4 >4 >4 31 1A-24 8 4 0.12 >4 >4 >4 >4 >4 >4 32 1A-25 0.25 0.12 0.12 8 2 4 8 8 >128 1A-26 0.25 0.12 0.06 1 2 0.5 >4 >4 >4 34 1A-27 >1 >1 >1 >1 >1 >1 >1 >1 >1 1A-28 0.06 0.015 0.03 1 0.25 2 8 16 >16 1A-29 0.5 0.25 1 32 8 16 >64 >64 >64 37 S-(+)- 1A-6 2 1 0.5 4 2 2 >4 >4 >4 GNA 1312 WO 33 38 R-(-)- 1A-6 0.12 0.06 0.12 1 0.5 0.25 >4 >4 >4 39 R-(-)-1A-2 0.12 0.06 0.06 2 0.25 0.5 2 >4 >4 S-(+)-1A-2 1 0.5 1 >4 2 2 >4 >4 >4 41 S-(+)-1A-13 0.5 0.25 0.25 >4 2 4 >4 >4 >4 42 R-(-)-1A-13 0.12 0.03 0.03 2 0.12 0.5 >4 >4 >4 A: MIC in μg/ml; B: MIC in μg/ml 80 50 Ca01: C.albicans ATCC 24433; Cg01: C. glabrata ATCC 90030; Ck01: C. krusei ATCC 6258; Ct01: C. tropicalis ATCC 750; Cn01: C. neoformans ATCC 34664; Afm01: A. fumigatus ATCC 46645; An01:A. niger ATCC 16404; Fp01: F. proliferatum ATCC 10052.

*For azoles: For Fluconazole and the NCEs, MIC is recorded as the concentration exhibiting 80% inhibition as compared to the positive control.

For Amphotericin B: MIC is recorded as the concentration exhibiting complete inhibition.

It will be evident to those skilled in the art that the invention is not limited to the details of the foregoing illustrative examples and that the present invention may be embodied in other specific forms without departing from the essential attributes thereof, and it is therefore desired that the present embodiments and examples be considered in all respects as illustrative and not restrictive, reference being made to the appended claims, rather than to the foregoing description, and all changes which come within the meaning and range of equivalency of the claims are therefore intended to be embraced therein.

GNA 1312 WO 34

Claims

We claim,

1. Antifungal compounds of Formula (1) and pharmaceutically acceptable salts thereof; 1 1 1 1 R A -B -C Formula 1 wherein, X and Y may be same or different, and each represents hydrogen or halogen selected from fluorine, chlorine or bromine; Z is hydrogen, optionally substituted alkyl containing 1 to 5 carbon atoms, optionally substituted allyl, -COCH or optionally substituted phenyl; 1 2 3 4 R , R , R and R may be same or different, and each represents hydrogen or functional groups selected from alkyl group of linear or branched chain of 1 to 20 carbon atoms optionally substituted with phenyl group, alkoxy (-OR) group (wherein R= alkyl group with 1 to 4 carbon atoms), hydroxyl group, halogen selected from fluorine, chlorine, bromine or iodine, or nitro group; A and B are different, and represent –C=O, -CH=CH-, optionally substituted alkyl group of linear or branched chain of 1 to 20 carbon atoms, aziridinyl, epoxy ring, -CH(OR ) wherein R is H, alkyl group with 1 to 4 carbon atoms, acyl or 6 6 7 7 phenyl, -C=N-OR wherein R is H ormethyl, -C=N-R wherein R is alkyl group of linear or branched chain of 1 to 20 carbon atoms or phenyl, -C(X’R )Y’R wherein X’ and Y’ may be same or different and each represents -O or -S, and R 9 8 9 and R represents alkyl group with 1 to 4 carbon atoms or phenyl or R and R are linked with each other to form a (hetero)cyclic five to eight-membered ring; or GNA 1312 WO 35 A and B together represent heterocyclic ring selected from 3,5-disubstituted (1H)-pyrazole or 3,5-disubstituted 4,5-dihydro(1H)-pyrazole; C represents hydrogen, optionally substituted phenyl, optionally substituted pyridyl, optionally substituted thienyl, optionally substituted naphthyl, optionally substituted anthracenyl, optionally substituted indolyl, optionally substituted cycloalkyl or optionally substituted alkyl group of linear or branched chain of 1 to 20 carbon atoms. ‘*’ is used to designate R or S configuration at carbon atom or racemic nature of the compound.

2. The antifungal compounds of Formula 1 as claimed in claim 1, wherein; 1 1 1 1 a) A is –C=O when B is –CH=CH- ;or A is –CH=CH- when B is –C=O; or 1 1 1 b) A is –C=O when B is optionally substituted alkyl or epoxy ring; or A is optionally substituted alkyl or epoxy ring when B is –C=O; or 1 1 5 6 7 8 9 c) A is –CH=CH- when B is -CH(OR ), -C=N-OR -C=N-R or -C(X’R )Y’R 1 5 6 7 8 9 1 ; or A is-CH(OR ), -C=N-OR -C=N-R or -C(X’R )Y’R when B is – CH=CH-, or d) A and B together represent 3,5-disubstituted (1H)-pyrazole, or e) A and B together represent 3,5-disubstituted 4,5-dihydro(1H)-pyrazole,

3. The compounds according to claim 1 are selected from a group consisting of: (E)(4-(2-(2,4-Difluorophenyl)hydroxy(1H-1,2,4-triazolyl)propoxy) phenyl) phenylpropenone; (E)(4-(2-(2,4-Difluorophenyl)hydroxy(1H-1,2,4-triazol l)propoxy)phenyl)(4-methoxyphenyl)propenone; (E)(4-(2-(2,4-Difluorophenyl)hydroxy(1H-1,2,4-triazol l)propoxy)phenyl)(2-methoxyphenyl)propenone; (E)(4-(2-(2,4-Difluorophenyl)hydroxy(1H-1,2,4-triazol l)propoxy)phenyl)(3,5-dimethoxyphenyl)propenone; GNA 1312 WO 36 (E)(4-(2-(2,4-Difluorophenyl)hydroxy(1H-1,2,4-triazol l)propoxy)phenyl)(3,4,5-trimethoxyphenyl)propenone; (E)(4-Chlorophenyl)(4-(2-(2,4-difluorophenyl)hydroxy(1H-1,2,4- triazolyl)propoxy)phenyl)propenone; (E)(2,4-dichlorophenyl)(4-(2-(2,4-difluorophenyl)hydroxy(1H-1,2,4- triazolyl)propoxy)phenyl)propenone; (E)(4-(2-(2,4-Difluorophenyl)hydroxy(1H-1,2,4-triazolyl)propoxy) phenyl) (2-fluorophenyl)propenone; (E)(4-(2-(2,4-Difluorophenyl)hydroxy(1H-1,2,4-triazolyl)propoxy) phenyl)(4-(octyloxy)phenyl)propenone; (E)(4-(2-(4-Fluorophenyl)hydroxy(1H-1,2,4-triazol yl)propoxy)phenyl)(4-methoxyphenyl)propenone; (E)(4-(2-(4-Bromophenyl)hydroxy(1H-1,2,4-triazol yl)propoxy)phenyl)(4-methoxyphenyl)propenone; (E)(4-Chlorophenyl)(4-(2-(4-fluorophenyl)hydroxy(1H-1,2,4-triazol- 1-yl)propoxy)phenyl)propenone; (E)(4-(2-(2,4-Difluorophenyl)hydroxy(1H-1,2,4-triazolyl)propoxy) phenyl)(thiophenyl)propenone; (E)(4-(2-(2,4-Difluorophenyl)hydroxy(1H-1,2,4-triazolyl)propoxy) phenyl)(naphthalenyl)propenone; (E)(Anthracenyl)(4-(2-(2,4-difluorophenyl)hydroxy(1H-1,2,4- triazolyl)propoxy)phenyl)propenone; (E)(4-(2-(2,4-Difluorophenyl)hydroxy(1H-1,2,4-triazolyl)propoxy) phenyl)(1-methyl-1H-indolyl)propenone; (E)(4-(2-(4-Fluorophenyl)hydroxy(1H-1,2,4-triazol yl)propoxy)phenyl)(thiophenyl)propenone; (E)(4-(2-(2,4-Difluorophenyl)hydroxy(1H-1,2,4-triazolyl)propoxy) phenyl)(4-methoxyphenyl)propenone; (E)(4-(2-(2,4-Difluorophenyl)hydroxy(1H-1,2,4-triazolyl)propoxy) phenyl)(p-tolyl)propenone; (E)(2,4-Dichlorophenyl)(4-(2-(2,4-difluorophenyl)hydroxy(1H-1,2,4- triazolyl)propoxy)phenyl)propenone; GNA 1312 WO 37 (E)(4-(2-(2,4-Difluorophenyl)hydroxy(1H-1,2,4-triazolyl)propoxy) methoxyphenyl)(4-methoxyphenyl)propenone; (E)(4-(2-(2,4-Difluorophenyl)hydroxy(1H-1,2,4-triazolyl)propoxy) phenyl)(4-(octyloxy)phenyl)propenone; (E)(4-(2-(2,4-Difluorophenyl)hydroxy(1H-1,2,4-triazolyl)propoxy) phenyl)butenone; (E)(4-(2-(2,4-Difluorophenyl)hydroxy(1H-1,2,4-triazolyl)propoxy) phenyl)octenone; (E)(4-(2-(2,4-Difluorophenyl)hydroxy(1H-1,2,4-triazolyl)propoxy) phenyl)heptadecenone; (E)Cyclopropyl(4-(2-(2,4-difluorophenyl)hydroxy(1H-1,2,4-triazol yl) propoxy)phenyl)propenone; (E)(4-(2-(2,4-Difluorophenyl)hydroxy(1H-1,2,4-triazolyl)propoxy) methoxyphenyl)acrylaldehyde; 2,3-Dibromo(2,4-dichlorophenyl)(4-(2-(2,4-difluorophenyl)hydroxy (1H-1,2,4-triazolyl)propoxy)phenyl)propanone; (3-(2,4-Dichlorophenyl)oxiranyl)(4-(2-(2,4-difluorophenyl)hydroxy(1H- 1,2,4-triazolyl)propoxy)phenyl)methanone; (E)(2,4-Dichlorophenyl)(4-(2-(2,4-difluorophenyl)hydroxy(1H-1,2,4- triazolyl)propoxy)phenyl)propenol; 1-(4-(5-(2,4-Dichlorophenyl)-1H-pyrazolyl)phenoxy)(2,4-difluorophenyl)- 3-(1H-1,2,4-triazolyl)propanol ; 1-(4-(5-(2,4-Dichlorophenyl)-4,5-dihydro-1H-pyrazolyl)phenoxy)(2,4- difluorophenyl)(1H-1,2,4-triazolyl)propanol ; (E)(2,4-dichlorophenyl)(4-(2-(2,4-difluorophenyl)methoxy(1H-1,2,4- triazolyl)propoxy)phenyl)propenone ; (E)(4-(2-(Allyloxy)(2,4-difluorophenyl)(1H-1,2,4-triazolyl)propoxy) phenyl)(2,4-dichlorophenyl)propenone ; S-(+)-(E)(4-chlorophenyl)(4-(2-(2,4-difluorophenyl)hydroxy(1H- 1,2,4-triazolyl)propoxy)phenyl)propenone; R-(-)-(E)(4-(2-(2,4-Difluorophenyl)hydroxy(1H-1,2,4-triazolyl) propoxy) phenyl)(4-methoxyphenyl)propenone; GNA 1312 WO 38 S-(+)-(E)(4-(2-(2,4-Difluorophenyl)hydroxy(1H-1,2,4-triazolyl) propoxy) phenyl)(4-methoxyphenyl)propenone; S-(+)-(E)(4-(2-(2,4-Difluorophenyl)hydroxy(1H-1,2,4-triazolyl) propoxy) phenyl)(thiophenyl)propenone ; R-(-)-(E)(4-(2-(2,4-Difluorophenyl)hydroxy(1H-1,2,4-triazolyl) propoxy) phenyl)(thiophenyl)propenone

4. The antifungal compounds of Formula 1 as claimed in claim 1, wherein Z is H and 1 1 1 1 A is –C=O when B is –CH=CH- ;or A is –CH=CH- when B is –C=O, are prepared i. reacting an epoxide of Formula 2 with a compound of Formula 3 in presence of a base, with or without a phase transfer catalyst, to obtain a compound of Formula 4, wherein the base is selected from potassium carbonate, sodium carbonate, cesium carbonate or lithium carbonate, and the phase transfer catalyst is selected from tetra-n-butylammonium bromide (TBAB), tetra-n-butylammonium chloride, benzyltriethylammonium bromide, benzyltriethylammonium chloride, cetyltri-n-butylphosphonium bromide, cetyltrimethylammonium bromide or cetyltrimethylammonium chloride, Formula 2 HO R Formula 3 Formula 4 GNA 1312 WO 39 wherein, D represents -CHO or -COCH and ii. reacting the compound of Formula 4 with an aldehyde/ketone in presence of a base selected from sodium hydroxide, potassium hydroxide, lithium hydroxide, sodium methoxide or potassium tert butoxide.

5. The antifungal compound of Formula 1 as claimed in claim 1, wherein Z is H and 1 1 1 1 A is –C=O when B is –CH=CH- ;or A is –CH=CH- when B is –C=O are prepared by reacting compound of Formula 2 with a substituted enone of Formula 5, in presence of a base with or without phase transfer catalyst, wherein the base is selected from potassium carbonate, sodium carbonate, cesium carbonate or lithium carbonate, and the phase transfer catalyst is selected from tetra-n-butylammonium bromide (TBAB), tetra-n-butylammonium chloride, benzyltriethylammonium bromide, benzyltriethylammonium chloride, cetyltri-n-butylphosphonium bromide, cetyltrimethylammonium bromide or cetyltrimethylammonium chloride, R A -B -C 1 1 1 1 HO R Formula 2 Formula 5.

6. The process for preparation of the antifungal compounds of Formula 1 as claimed in claim 4, wherein an aldehyde or ketone is selected from optionally-substituted aliphatic/aromatic/heteroaromatic aldehyde or ketone.

7. The antifungal compounds of Formula 1 as claimed in claim 1 wherein Z is optionally substituted alkyl containing 1 to 5 carbon atoms, optionally-substituted allyl, -COCH3 or optionally substituted phenyl and A is –C=O when B is –CH=CH- ; or A is –CH=CH- when B is –C=O, are prepared by reacting the compounds of 1 1 1 formula 1 wherein Z is H and A is –C=O when B is –CH=CH- ; or A is –CH=CH- 1 2 2 when B is –C=O, with a compound of formula ‘Z X’ wherein Z is optionally substituted alkyl containing 1 to 5 carbon atoms, optionally-substituted allyl, -COCH3 GNA 1312 WO 40 or optionally substituted phenyland X is a halogen selected from iodine, bromine or chlorine.

8. The antifungal compounds of Formula 1 as claimed in claim 1, wherein A is –C=O when B is optionally substituted alkyl or epoxy ring; or A is optionally substituted alkyl or epoxy ring when B is –C=O, are prepared by subjecting the 1 1 1 compounds of Formula 1 in which A is –C=O when B is –CH=CH- ; or A is –CH=CH- when B is –C=O to functional group transformations selected from halogenation, epoxidation or reduction of the unsaturated double bond (-CH=CH-) representing A or B .

9. The antifungal compounds of Formula 1 as claimed in claim 1, wherein A is 1 5 6 7 8 9 1 –CH=CH- when B is -CH(OR ), -C=N-OR -C=N-R or -C(X’R )Y’R ; or A is 5 6 7 8 9 1 -CH(OR ), -C=N-OR -C=N-R or -C(X’R )Y’R when B is –CH=CH-, are prepared by subjecting the compounds of Formula 1 in which A is –C=O when B is –CH=CH- ; or A is –CH=CH- when B is –C=O to functional group transformations selected from reduction, oximation or ketalization of the carbonyl group representing A or B .

10. The antifungal compounds of Formula 1 as claimed in claim 1, wherein A and B together represent 3,5-disubstituted (1H)-pyrazole, are prepared by reacting compound of Formula 1 in which A is –C=O when B is optionally substituted alkyl or epoxy ring; or A is optionally-substituted alkyl or epoxy ring when B is –C=O with hydrazine hydrate in presence of an acid selected from p-toluene sulfonic acid, acetic acid, propionic acid or trifluoroacetic acid.

11. The antifungal compound of Formula 1 as claimed in claim 1, wherein A and B together represent 3,5-disubstituted 4,5-dihydro(1H)-pyrazole, are prepared by 1 1 1 reacting compound of Formula 1 in which A is –C=O when B is –CH=CH- ; or A is –CH=CH- when B is –C=O with hydrazine hydrate in presence of an acid selected from p-toluene sulfonic acid, acetic acid, propionic acid or trifluoroacetic acid. GNA 1312 WO 41

12. A pharmaceutical composition comprising the antifungal compounds of Formula 1 according to any one of the preceding claims, in association with at least one pharmaceutically acceptable excipient.

13. Use of the compounds of Formula 1 according to any one of the preceding claims, for preparation of medicament useful for treatment or prevention of fungal infections.