USRE38962E1 - Diphenyl-triazole derivatives and their use as anti-gestative immuno-suppressant and anti-tumoral agents - Google Patents

Diphenyl-triazole derivatives and their use as anti-gestative immuno-suppressant and anti-tumoral agents Download PDF

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Publication number
USRE38962E1
USRE38962E1 US10/178,305 US17830500A USRE38962E US RE38962 E1 USRE38962 E1 US RE38962E1 US 17830500 A US17830500 A US 17830500A US RE38962 E USRE38962 E US RE38962E
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saturated
heterocyclic aromatic
hydrogen
alkyl
linear
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Carla Rossi
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Geange Ltd
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Geange Ltd
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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
    • C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00—Drugs for genital or sexual disorders; Contraceptives
    • A61P15/18—Feminine contraceptives
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/02—Immunomodulators
    • A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02—Phosphorus compounds
    • C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/645—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having two nitrogen atoms as the only ring hetero atoms
    • C07F9/6503—Five-membered rings
    • C07F9/65031—Five-membered rings having the nitrogen atoms in the positions 1 and 2
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02—Phosphorus compounds
    • C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/6515—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having three nitrogen atoms as the only ring hetero atoms
    • C07F9/6518—Five-membered rings

Definitions

  • Objects of the present invention are nitrogen heterocyclic aromatic derivatives and their use as anti-gestative, immunosuppressant and anti-tumoral agents.
  • Object of the present invention is also a procedure for the preparation of nitrogen heterocyclic aromatic derivatives.
  • Object of the present invention is again a pharmaceutical composition which contains, as active principle, at least one heterocyclic aromatic according to the present invention.
  • R 1 is an alkyl group C 1 -C 4 .
  • EP11129 reports 1,2,4 triazoles derivatives of the following general structure:
  • BE 879,732 reports a class of compounds showing the following general structure:
  • R is an hydrogen or a R 5 —CO group where R 5 is chosen among alkyl C 1 -C 4 , alkenyl C 2 -C 4 and alkinyl C 2 -C 4 , whereas R 2 is a —CH(R 7 )OR 8 where R 7 is an hydrogen or methyl and R 8 is like R 5 —CO.
  • the pharmacological data show how these compounds display a high anti-gestative activity after repeated parenteral administrations (daily up to 5 consecutive days).
  • the literature describes the compound 3-(2-ethyl-phenyl)-5-(3-methoxy-phenyl)-1H-1,2,4-triazole, also identified by the code DL 111-IT (Reviews on Drug Metabolism & Drug Interactions, Vol. IV, N. 2&3, 1982, A. Assandri, A: Omodei-Sale', G. Galliani).
  • DL 111-IT reported in BE 879,732 did show an interesting anti-gestative activity in all the investigated animal species including the mouse, the rat, the hamster, the dog and monkeys.
  • DL 111-IT has been proposed as anti-gestative agent for human use.
  • EP0080053 describes 3,5 diphenyl-1H-1,2,4 triazole derivatives that, as compared to the previously reported derivatives, have been structurally modified in order to obtain a high anti-gestative activity after a single-dose parenteral administration by subcutaneous and intramuscular route.
  • Objective of the present invention is to make available nitrogen heterocyclic aromatic derivatives endowed with high anti-gestative activity when administered as single dose to different animal species including higher mammals and man.
  • Objective of the present invention is also to make available nitrogen heterocyclic aromatic derivatives endowed with high immuno-suppressant activity.
  • objective of the present invention is to make available nitrogen heterocyclic aromatic derivatives endowed with non species-specific anti-gestative, immuno-suppressant and anti-tumour activity.
  • objective of the present invention is to make available nitrogen heterocyclic aromatic derivatives endowed with a sustained duration of action, thus able to display the desired activity by a single-dose treatment (anti-gesative activity) or by multiple dose treatments with wide inter-administration time intervals (immuno-suppressant and anti-tumor acitvities).
  • Objective of the present invention is also to make available a pharmaceutical formulations, containing at least one nitrogen heterocyclic aromatic derivative as active principle, easy to be administered, well tolerated and able to allow a high therapeutic index.
  • the mentioned nitrogen heterocyclic aromatic derivative of formula (I) is a derivative of imidazole and 1H-1,2,4-triazole respectively:
  • the mentioned derivative of formula (I) is a triazole derivative having the following general formula:
  • R 6 is hydrogen
  • R 4 is —OCH 3 or —OCH 2 CH 3
  • R 3 is hydrogen
  • the derivatives of the present invention are provided of anti-gestation, immuno-suppressive and anti-tumour activities. Particularly, the anti-gestative activity is displayed by a single dose regime and it does not requires a prolonged treatment. Furthermore, these derivatives show high therapeutic indexes, since a remarkable efficacy is achieved at doses much lower than the toxic ones able to induce undesirable adverse events.
  • the compounds of the present invention of formula (I) when administered as a single parenteral injection displayed more than one pharmacological activity, namely:
  • the different pharmacological activities displayed by the derivatives object of the present invention are attributable to a common mechanism of action.
  • the reference model which explains this multiple pharmacological action is an atypical rapidly poliferating cell system, the placenta.
  • placenta As repcorted Aitken, Beaconsfield and Ginsher in their comprehensive review origin and formation of the placenta this system, during its early stage of development, has strong similarties to tumor (1).
  • the placenta is tolerated by the maternal host due to an alteration of the immune responsiveness with no inflammatory response to blastocyst and/or throphoblast invasion.
  • the derivatives object of the present invention are characterised by the presence of an easily hydrolysed bond through non species-specific enzymatic reactions occurring on R 5 group; this hydrolysis allows the release of the active principle that can display its in vivo action.
  • the characteristic bond of R 5 group present in the derivatives object of the present invention is different from the bonds described in the already disclosed derivatives, and it can be hydrolysed according to different mechanisms of reaction. Because of these properties, unlike the compounds already disclosed, the compounds objective of the present invention are also effective in higher mammal species, including humans.
  • the pregnancy-terminating activity of the compounds of the present invention has been assessed by carrying out experiments in rats and dogs.
  • Pregnancy was later confirmed at the time of autopsy by the presence of implantation sites in the uterus.
  • compound D active principle
  • compound E prepared as described in BE 879732 and identified as DL111-IT
  • Table 2 Pregnancy Termination Activity in S.D. Rats After a Single Subcutaneous Injection at Day 7 of Gestation
  • the compound was given intramuscularly in one depot site of the thigh muscle of the right hind leg dissolved in sesame oil at the dose of 5 mg/kg (11.1 ⁇ moles/kg , 40 mg/mL, 0.2 mL/kg).
  • the anti-gestative effectiveness was ascertained by exploratory laparatomy examining uterine horns where the presence of live or dead foetuses was deduced from the dimension and appearance of each uterine swelling, for methodological reference see G. Galliani et al., J. Small Animal Practice, 25, 211-222 (1984).
  • the compounds of the present invention displayed significant immuno-suppressive activity on both humoral and cellular immunity when administered during the inductive phase of the immuno response, i.e. soon after antigen challenge.
  • immuno-suppressive activity on both humoral and cellular immunity when administered during the inductive phase of the immuno response, i.e. soon after antigen challenge.
  • experimental models of auto-immunity and skin transplantation they were able to reduce auto-antibody production as well as to prolong the skin graft survival.
  • the immuno-suppressant activity of the compounds of the present invention was assessed by carrying out experiments in mice.
  • SRBC Sheep Red Blood Cells
  • LPS Lipo-polysaccharide
  • Indirect PCF were developed with rabbit anti-serum to mouse gamma globulin.
  • B6D2F1 mice were immunised with 20 ⁇ g LPS intra-peritoneally.
  • PCF were determined in the spleen by SRBC coated with LPS, Moller, Nature, 207, 1166(1965).
  • DTH Delayed Type hypersensitivity
  • the compounds of the present invention are endowed with a high and specific anti-tumour activity as demonstrated on an in vivo test against human chario-carcinoma.
  • compound of example 5 was highly effective in inhibiting the growth of a human chorio-carcinoma transplanted into nude mice.
  • the potency of the tested compound was even higher than that displayed by methotrexate, the choice drug in the therapy of chorio-carcinoma.
  • choriocarcinoma is a gestational tumor derived from trophoblastic cells, which, together with decidual cells, was suggested as the target site of the anti-proliferative action or 3,5 diaryl-s-1,2,4 triazoles (Galliani et al. 1986).
  • the compounds of the present invention are embodied into topical, transdermal and injectable dosage forms to be administered epicutaneously or parenterally, i.e. subcutaneously, intramuscularly or intravenously.
  • Such composition are formulated using proper transdermal delivery systems (epicutaneous dosing), aqueous (intravenous dosing) or non-aqueous vehicles (epicutaneous, subcutaneous and intramuscular dosing).
  • oils of vegetable origin or fatty esters such as sesame oil, corn oil, peanut oil, cotton seed oil, and ethyl oleate can suitably be employed.
  • oily vehicles may as well be used provided that they are safe in the volume administered and do not interfere with the therapeutic efficacy of the preparation.
  • these preparations may also contain anti-microbial agents, to prevent growth of micro-organisms in the preparation, and antioxidants, essentially to prevent the development of rancidity of the oily vehicle.
  • dosage forms in general contain from 1 to 10% (w/v) of at least one derivative or formula (I) object of the present invention, where the optimum dose/volume ratio depends on the selected dose and the species and size of the animal/subject to be administered
  • the compounds of the present invention can be advantageously prepared starting from a derivative (IX) of the following chemical formula.
  • This method consists in the rearrangement of hydrazones of substituted benzaldehydes with 4-hydrazino-1H-2,3-benzoxazines of formula (X) wherein R 1 , R 2 and R 3 are as defined as for the derivatives of formula (I).
  • This rearrangement simply occurs by refluxing the hydrazone III in a high boiling inert organic solvent, such as for instance, xylene, N,N-dimethylformamide, and halogenated aromatic hydrocarbons, for about 30 minutes and then recovering the compound II by filtration.
  • a high boiling inert organic solvent such as for instance, xylene, N,N-dimethylformamide, and halogenated aromatic hydrocarbons
  • Another suitable method for the preparation of the 2-hydroxymethyl-phenyl derivatives of formula (XI a), consists in the oxidation of the corresponding 2-methylphenyl triazoles, either directly to the alcohol (XI a) or to the corresponding carboxylic acid followed by a reduction of this latter to the alcohol (XI a).
  • ceric ammonium nitrate or silver (II)oxide are the oxidising agents which may be suitably employed, while in the latter, the oxidative step is carried out with any of the several oxidisers known in the art to transform a methyl group on an aromatic ring to a carboxylic group, such as permanganate, nitric acid, and dichromate, and the reductive step in easily performed with a metal hydride.
  • the starting compounds of formula II can be prepared by following the process described in EP80053.
  • derivative of formula (IX) when have to be synthesised derivatives of formula (I) where R 7 is chosen as (XII), asymmetric carbonates, or when R 7 is chosen as saturated or unsaturated, linear or branched C 1 -C 20 aliphatic hydrocarbon, derivative of formula (IX) can undergo reaction according to the following general scheme, in detail:
  • a tetrahydrofuran solution containing the imidazolide of the selected alcohol obtained by reacting the alcoholic derivative (10 mmoles) with 1,1′-carbonyl-diimidazole (1.65 g, 10 mmoles) in tetrahydrofuran (20 mL) for 1 hour at room temperature.
  • the mixture is stirred at room temperature for 12 hours, then solvent is take to dryness under vacuum and the residue re-dissolved in methylene chloride.
  • the organic phase is washed with water, dried by anhydrous Na 2 SO 4 and evaporated under vacuum.
  • the obtained crude material is purified by column chromatography on silica gel (eluent hexane-ethylacetate, 8:2, v/v). After evaporation of the solvents, the solid pure product obtained is re-dissolved in hexane, filtered and dried under vacuum.
  • R is chosen equal to —CO R 8 , where R 8 is a saturated or a non saturated C 1 -C 10 aliphatic hydrocarbon
  • the hydroxy group of derivative (IX) will be protected according to known methods.
  • Protected derivative (IXb) will be also obtained and acylated according to known methods in order to introduce the —COR 8 group. Subsequently these acylated derivatives will be de-protected and allowed to react with phosgene as reported above.
  • Derivatives of formula (I) are advantageously prepared starting from derivative s of formula (IX) (eventually submitted to a previous acylation reaction as already described) by reaction with phosphoric acid or equivalents according to known methods. For example, following this procedure derivative (VIII), object of the present invention, is prepared.
  • the mixture can be separated into the single components by chemico-physical known methods.
  • the way a mixture can be resolved into the single components is a fractionated crystallisation, which take advantage of the different solubility of each compound in various solvents at different temperatures.
  • Suitable solvents that can be used for this method are chosen as an example, among hexane, ethyl-acetate, C 1 -C 4 alkyl ethers, methylen chloride, light petroleum ether and mixtures thereof.
  • Another example of a method useful for the separation of the isomer mixture is based on the use of preparative high pressure liquid chromatography (PHPLC), carried out on proper columns, for example filled with silica-gel esterified with octyl-silane or octyl-decylsilane.
  • PPLC preparative high pressure liquid chromatography
  • Other obvious procedures useful for resolving a mixture of isomers into the single components are intended to fall within the scopes of the invention.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Molecular Biology (AREA)
  • Biochemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Engineering & Computer Science (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Immunology (AREA)
  • Transplantation (AREA)
  • Gynecology & Obstetrics (AREA)
  • Endocrinology (AREA)
  • Reproductive Health (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Pyridine Compounds (AREA)
US10/178,305 1997-06-05 1998-06-04 Diphenyl-triazole derivatives and their use as anti-gestative immuno-suppressant and anti-tumoral agents Expired - Fee Related USRE38962E1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
IT97MI001328A IT1292091B1 (it) 1997-06-05 1997-06-05 Derivati eterociclici aromatici azotati,procedimento per la loro preparazione e loro impiego come antigestativi,immunosoppressori e
PCT/EP1998/003496 WO1998055463A1 (en) 1997-06-05 1998-06-04 Diphenyl-triazole derivatives and their use as anti-gestative, immuno-suppressant and anti-tumoral agents
US09/445,218 US6333343B1 (en) 1997-06-05 1998-06-04 Diphenyl-triazole derivatives and their use as anti-gestative, immuno-suppressant and anti-tumoral agents

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USRE38962E1 true USRE38962E1 (en) 2006-01-31

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US09/445,218 Ceased US6333343B1 (en) 1997-06-05 1998-06-04 Diphenyl-triazole derivatives and their use as anti-gestative, immuno-suppressant and anti-tumoral agents

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US (2) USRE38962E1 (enrdf_load_stackoverflow)
EP (1) EP0986544A1 (enrdf_load_stackoverflow)
JP (1) JP2002508757A (enrdf_load_stackoverflow)
IT (1) IT1292091B1 (enrdf_load_stackoverflow)
WO (1) WO1998055463A1 (enrdf_load_stackoverflow)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20050119261A1 (en) * 2003-03-18 2005-06-02 Chakravarty Prasun K. Biaryl substituted triazoles as sodium channnel blockers
US20060183897A1 (en) * 2003-03-18 2006-08-17 Chakravarty Prasun K Biaryl substituted triazoles as sodium channel blockers

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4459302A (en) * 1978-10-30 1984-07-10 Gruppo Lepetit, S.P.A. Acyl-1H-1,2,4-triazole derivatives
US4535090A (en) * 1981-10-20 1985-08-13 Gruppo Lepetit S.P.A. 3,5-Diphenyl-1H-1,2,4-triazoles pharmaceutical compositions and uses
US4888350A (en) * 1978-10-30 1989-12-19 Gruppo Lepetit S.P.A. New acyl-1H-1,2,4-triazole derivatives

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SU508198A3 (ru) * 1971-07-22 1976-03-25 Группо Лепетит С.П.А. (Фирма) Способ получени производных 1,2,4-триазола

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4459302A (en) * 1978-10-30 1984-07-10 Gruppo Lepetit, S.P.A. Acyl-1H-1,2,4-triazole derivatives
US4888350A (en) * 1978-10-30 1989-12-19 Gruppo Lepetit S.P.A. New acyl-1H-1,2,4-triazole derivatives
US4535090A (en) * 1981-10-20 1985-08-13 Gruppo Lepetit S.P.A. 3,5-Diphenyl-1H-1,2,4-triazoles pharmaceutical compositions and uses

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20050119261A1 (en) * 2003-03-18 2005-06-02 Chakravarty Prasun K. Biaryl substituted triazoles as sodium channnel blockers
US20060183897A1 (en) * 2003-03-18 2006-08-17 Chakravarty Prasun K Biaryl substituted triazoles as sodium channel blockers
US7326726B2 (en) * 2003-03-18 2008-02-05 Merck & Co., Inc. Biaryl substituted triazoles as sodium channel blockers
US20080171777A1 (en) * 2003-03-18 2008-07-17 Chakravarty Prasun K Biaryl substituted triazoles as sodium channel blockers
US7572822B2 (en) 2003-03-18 2009-08-11 Merck & Co. Inc. Biaryl substituted triazoles as sodium channel blockers

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IT1292091B1 (it) 1999-01-25
JP2002508757A (ja) 2002-03-19
EP0986544A1 (en) 2000-03-22
ITMI971328A1 (it) 1998-12-05
ITMI971328A0 (enrdf_load_stackoverflow) 1997-06-05
US6333343B1 (en) 2001-12-25
WO1998055463A1 (en) 1998-12-10

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