Patent Application
20090076067
The invention relates to a pharmaceutical composition and a novel compound as an active ingredient thereof. Particularly, the compound according to the invention is useful for treatment of diseases associated with protozoa infection such as malaria including drug-resistant malaria, leishmania, trypanosomiasis including African sleeping sickness and Chagas disease, toxoplasmosis, and cryptosporidiosis.
Many infections caused by parasitic protozoa are known especially in tropical and subtropical regions. The infections include malaria, leishmania, African sleeping sickness (African trypanosomiasis), Chagas disease (American trypanosomiasis), lymphatic filariasis, babesiosis, cryptosporidiosis, and toxoplasmosis. Some diseases infect only human, others are zoonotic infections which infect humans, livestocks, and small animals. Either infection causes significant economic and social damage in the society.
Unfortunately, some of these diseases have no effective therapeutic agent so far, some causative protozoa develop drug-resistant mutant that is diffusing now, and some therapeutic agents against these diseases cause adverse effect. Effective drug with less adverse effect is highly desirable. Some of diseases develop serious symptoms which prevent a sufferer from leading ordinary social life, confines a sufferer to bed needing nursing care, or develops fatal symptoms. Drugs to be used for chemical therapy for these diseases are indispensable. However, effective vaccines against these diseases have not been developed yet, and cannot be anticipated in the foreseeable future. In this circumstance, medicine for chemical therapy which can be administered orally or by injection, or some other administration route are essential.
It is already known that a chemical compound represented by general formula (2) or (6) according to the invention as a water-soluble methine compound can be used as a material in photography, or antitumor medicine (Japanese patent application publication No. 1994-220053, 1994-293642). However, the applications do not disclose its usage as a therapeutic and/or prophylactic agent against protozoa infection.
The inventors already have disclosed that the rhodacyanines compound represented by general formula (9), which is relatively similar to the compound represented by general formula (2) of the invention, shows in vitro proliferation inhibition activity against malaria protozoa (Japanese patent application publication No. 2000-191531, 2003-034641, 2003-034642) and leishmania protozoa (Japanese patent application publication No. 2004-331545). The inventors also have disclosed that the rhodacyanines compound represented by general formula (10), which is relatively similar to the compound represented by general formula (3) of the invention, shows in vitro proliferation inhibition activity against malaria protozoa (Japanese patent application publication No. 2003-034640). However, the relationship between therapeutic effect against protozoa infections and molecular structure of the compound has not been elucidated yet. It is not known to those skilled in the art and cannot be anticipated that the azarhodacyanine compounds represented by general formulae (1) to (3), (6) and (7) according to the invention are effective as a therapeutic agent against protozoa infections.
Therapeutic effect of the compounds represented by the above general formulae (9) and (10) already known in the art was evaluated using malaria infected model animals (in vivo test) They only show 50% or less proliferation inhibition activity against malaria protozoa and survival benefit for one day at most at any dose or by any administration route. In general, therapeutic effect of an agent against malaria is evaluated in vivo based on proliferation inhibition activity and survival benefit. High proliferation inhibition activity and prolonged survival period is desirable.
The known compounds represented by general formulae (9) and (10) exert acute toxicity to a mouse. When they are intraperitoneally administered at dose of 20 mg/kg or more, all the treated mice died within 24 hours after administration.
Japanese patent application publication No. 1994-220053
Japanese patent application publication No. 1994-293642
Japanese patent application publication No. 2000-191531
Japanese patent application publication No. 2003-034641
Japanese patent application publication No. 2003-034642
Japanese patent application publication No. 2004-331545
Japanese patent application publication No. 2003-034640
Therefore, an object of the invention is to provide a pharmaceutical composition which can be used as a therapeutic and/or prophylactic agent with high therapeutic effect on the infection caused by parasitic protozoa and selective toxicity against the causative protozoa. Particularly, an object of the invention is to provide a pharmaceutical composition which can be used as a therapeutic and/or prophylactic agent, has low toxicity to the human suffering form infection by parasitic protozoa, and shows significant therapeutic effect when administered.
In order to solve the above problems, the inventors measured proliferation inhibition effect of a variety of compounds against causative protozoa, and evaluated cytotoxic effect on mammalian cells as an indicator of adverse effect. As to selected compounds, therapeutic effect against malaria was evaluated by administering it in ranging dose through various administration routes using malaria infected mice as a model host, in order to select a compound which shows at least 50% of proliferation inhibition effect against malaria protozoa. As a result, it was found that the object of the invention as above can be achieved by pharmaceutical composition containing a compound represented by following general formula as an active ingredient. The invention is completed based on this finding.
Some aspects of the invention are as follows.
wherein, R1 and R4 respectively represents alkyl group which may be the same or different from each other, R2 and R3 respectively represents alkyl, aryl, or heterocyclic group, X1 and X2 respectively represents S, O, Se, —CR5R6- (R5 and R6 respectively represents alkyl group), —NR7- (R7 represents alkyl, aryl, or heterocyclic group), or —CR8-CR9- (R8 and R9 represents hydrogen or substituent, alternatively, R8 and R9 may bind together to form alicyclic ring, aromatic ring, or heterocyclic ring), Y1 and Y2 respectively represents S, O, Se, or —NR8- (R8 is an alkyl, aryl, or heterocyclic group), Z1 and Z2 respectively represents an atomic group necessary for forming a five member ring or a six member ring, L1 and L2 respectively represents methine group, wherein p>0 and L1 is a substituted methane group, L1 and R1 may bind together to form a five member ring or a six member ring, Q represents physiologically acceptable anion, k represents one integer from 0 to 2 necessary to null whole molecular charge, m and n respectively represents 0 or 1 which may be same or different from each other, p represents one integer from 0 to 2, and q represents one integer from 0 to 2.
wherein R1 and R3 respectively represents alkyl group which may be the same or different from each other, R2 represents alkyl, aryl, or heterocyclic group, X1 and X2 respectively represents S, O, Se, —CR4R5- (R4 and R5 respectively represents alkyl group), —NR6- (R6 represents alkyl, aryl, or heterocyclic group), or —CR7=CR8- (R7 and R8 represents hydrogen or substituent, alternatively, R7 and R8 may bind together to form alicyclic ring, aromatic ring, or heterocyclic ring), Z1 and Z2 respectively represents atomic group necessary for forming a five member ring or a six member ring, Q represents physiologically acceptable anion, k represents one integer from 0 to 2 necessary to null whole molecular charge, and m and n respectively represent 0 or 1 which may be same or different from each other.
wherein, R1 and R4 respectively represents alkyl group which may be the same or different from each other, R2 and R3 respectively represents alkyl, aryl, or heterocyclic group, X1 and X2 respectively represents S, O, Se, —CR5R6- (R5 and R6 respectively represents alkyl group), —NR7- (R7 represents alkyl, aryl, or heterocyclic group), or —CR8=CR9- (R8 and R9 represents hydrogen or substituent, alternatively, R8 and R9 may bind together to form alicyclic ring, aromatic ring, or heterocyclic ring), Z1 and Z2 respectively represents atomic group necessary for forming a five member ring or a six member ring, Q represents physiologically acceptable anion, k represents one integer from 0 to 2 necessary to null whole molecular charge, and m and n respectively represents 0 or 1 which may be same or different from each other.
wherein, R1 and R10 respectively represents alkyl group which may be same or different from each other, R2 represents alkyl, aryl, or heterocyclic group, X1 represents S, O, Se, —CR5R6- (R5 and R6 respectively represents alkyl group), —NR7- (R7 represents alkyl, aryl, or heterocyclic group), or —CR8=CR9- (R8 and R9 represents hydrogen or substituent, alternatively, R8 and R9 may bind together to form alicyclic ring, aromatic ring, or heterocyclic ring), Z1 represents an atomic group necessary for forming a five member ring or a six member ring, Q represents physiologically acceptable anion, k represents one integer from 0 to 2 necessary to null whole molecular charge, and m represents 0 or 1,
wherein, R4 represents alkyl group, R3 represents alkyl, aryl, or heterocyclic group, X2 represents S, O, Se, —CR5R6- (R5 and R6 respectively represents alkyl group), —NR7- (R7 represents alkyl, aryl, or heterocyclic group), or —CR8=CR9- (R8 and R9 represents hydrogen or substituent, alternatively, R8 and R9 may bind together to form alicyclic ring, aromatic ring, or heterocyclic ring), Z2 represents an atomic group necessary for forming a five member ring or a six member ring, Q represents physiologically acceptable anion, k represents one integer from 0 to 2 necessary to null whole molecular charge, and n represents 0 or 1.
wherein, R1 and R3 respectively represents alkyl group which may be same or different from each other, R2 represents alkyl, aryl, or heterocyclic group, X1 and X2 respectively represents S, O, Se, —CR4R5- (R4 and R5 respectively represents alkyl group), —NR6- (R6 represents alkyl, aryl, or heterocyclic group), or —CR7=CR8- (R7 and R8 represent hydrogen or substituent, alternatively, R7 and R8 may bind together to form alicyclic ring, aromatic ring, or heterocyclic ring), Z1 and Z2 respectively represents an atomic group necessary for forming a five member ring or a six member ring, Q represents physiologically acceptable anion, k represents one integer from 0 to 2 necessary to null whole molecular charge, and m and n represent 0 or 1 which may same or different from each other.
wherein, R1 and R4 respectively represents alkyl group which may be the same or different from each other, R2 and R3 respectively represents alkyl, aryl, or heterocyclic group, X1 and X2 respectively represents S, O, Se, —CR5R6- (R5 and R6 respectively represents alkyl group), —NR7- (R7 represents alkyl, aryl, or heterocyclic group), or —CR8=CR9- (R8 and R9 represents hydrogen or substituent, alternatively, R8 and R9 may bind together to form alicyclic ring, aromatic ring, or heterocyclic ring), Z1 and Z2 respectively represents atomic group necessary for forming a five member ring or a six member ring, Q represents physiologically acceptable anion, k represents one integer from 0 to 2 necessary to null whole molecular charge, and m and n respectively represents 0 or 1 which may be same or different from each other.
wherein, R1 and R10 respectively represents alkyl group which may be the same or different from each other, R2 represents alkyl, aryl, or heterocyclic group, X1 represents S, O, Se, —CR5R6- (R5 and R6 respectively represents alkyl group), —NR7- (R7 represents alkyl, aryl, or heterocyclic group), or —CR8=CR9- (R8 and R9 represents hydrogen or substituent, alternatively, R8 and R9 may bind together to form an alicyclic ring, aromatic ring, or heterocyclic ring), Z1 represents an atomic group necessary for forming a five member ring or a six member ring, Q represents physiologically acceptable anion, k represents one integer from 0 to 2 necessary to null whole molecular charge, and m represents 0 or 1,
wherein, R4 represents alkyl group, R3 represents alkyl, aryl, or heterocyclic group, X2 represents S, O, Se, —CR5R6- (R5 and R6 respectively represents alkyl group), —NR7- (R7 represents alkyl, aryl, or heterocyclic group), or —CR8=CR9- (R8 and R9 represents hydrogen or substituent, alternatively, R8 and R9 may bind together to form alicyclic ring, aromatic ring, or heterocyclic ring), Z2 represents an atomic group necessary for forming a five member ring or a six member ring, Q represents physiologically acceptable anion, k represents one integer from 0 to 2 necessary to null whole molecular charge, and n represents 0 or 1.
The compound contained as an active ingredient in the pharmaceutical composition according to the invention shows proliferation inhibition effect at low-dose against parasite protozoa, and shows no cytotoxic effects on mammalian cells at dose higher than the dose having proliferation inhibition effect (namely, selective toxicity index is high). In an in vivo treatment study using malaria infected mice, it is confirmed that the compound showed significantly higher recovery rate and prolonged survival compared to conventional compounds known in the art. Furthermore, it showed extremely low acute toxicity. Therefore, the compound is proved to be an effective therapeutic agent against malaria with improved adverse effect profile.
Next, the pharmaceutical composition according to the invention will be described in detail. In this specification, “the compound of the invention” includes all compounds according to the invention, represented by general formulae (1), (2), (3), (6) and (7). The compounds represented by general formulae (1) encompass compounds represented by general formulae (2), (3), (6) and (7). The compounds represented by general formula (3) and (7) are a novel compound that has not been known yet in the art. As described in the synthesis of compound in the present specification, the above novel compounds may be prepared from the above materials by any method known to those skilled in the art.
Preferable alkyl group in the general formula representing the compound of the invention includes alkyl group having 1 to 12 carbons, more preferably 1 to 6 carbons, and the alkyl group may be in linear, branched, or cyclic form. Particularly alkyl group includes methyl, ethyl, and butyl group. Preferable aryl group in the general formula includes aryl having 5 to 15 carbons, more preferably 6 to 10 carbons. Particularly aryl group includes phenyl group, tolyl group and p-chlorophenyl group.
Preferable heterocyclic group in the general formula representing the compound of the invention is 5 to 8 member group, more preferably, 5 or 6 member group. Hetero atom includes atoms of nitrogen, oxygen, sulfur, selenium, tellurium, and phosphorous. Preferably they are atoms of nitrogen, oxygen, sulfur or selenium. Particularly heterocyclic group includes pyrrole ring, furan ring, piperidine ring, morpholine ring, piperazine ring, pyridine ring, and pyrrolidine ring. The heterocyclic group may be substituted such as dihydropirrole ring, or tetrahydropyridine ring.
The alicyclic ring in the general formula representing the compound of the invention includes those known in the art, including cyclopentene ring and cyclohexane ring.
Aromatic ring in the general formula representing the compound of the invention includes those known in the art, including benzene ring and naphthalene ring.
R7, R8 and R9 in the general formula representing the compound of the invention are substituents well known in the art.
Preferable substituent includes alkyl group having 1 to 6 carbons such as methyl group, ethyl group, propyl group, and isopropyl group; alkenyl group having 2 to 6 carbons; alkynyl group having 2 to 6 carbons; alkoxy group having 1 to 6 carbons; aryloxy group having 6 to 8 carbons; aryl group having 6 to 8 carbons; aromatic group including phenyl group and naphthyl group; substituent amino group such as amino group, dialkylamino group, acylamino group, and sulfonylamino group; hydroxyl group; carbamoyl group; sulfamoyl group; acyloxy group having 2 to 6 carbons; carboxyl group; the alkoxycarbonyl group having 2 to 6 carbons; aminocarbonyl group; nitrile group; sulfonic acid group; nitro group; chloro group; fluoro group and bromo group. Alternatively, alkyl group, aryl group and other cyclic group as above in the general formula representing the compound of the invention may be substituted by these substituents.
In the above compound, Q is necessary for charge equilibrium. The term “physiologically acceptable anion” in the description of Q means that Q is an ion which is no toxic to the recipient when the compound is administered to the recipient and which makes the compound soluble in water. Preferable physiologically acceptable anion represented by Q includes, halogen ions such as chlorine ion, bromine ion, and iodine ion; sulfonate ion including fatty acid and aromatic sulfonate ion such as methansulfonate ion, trifluoromethanesulfonate ion, p-toluenesulfonate ion, naphthalenesulfonate ion, 2-hydroxyethansulfonate ion; sulfamate ion such as cyclohexanesulfamate ion; sulfate ion such as methylsulfate ion and ethylsulfate ion; hydrogensulfate ion; borate ion; alkyl and dialkyll phosphate ion such as diethylphosphate ion and methylhydrogen phosphate ion; pyrophosphate ion such as trimethylpyrophosphate ion; carboxylate ion (carboxylate ion having carboxy group and hydroxyl group substituted can be conveniently used); carbonate ion; hydrogen carbonate ion; perchlorate ion; and hydroxyl ion. Most preferable physiologically acceptable anion Q includes chlorine ion, acetate ion, propionate ion, valerate ion, citrate ion, maleate ion, fumarate ion, lactate ion, succinate ion, tartarate ion, benzoate ion, perchlorate ion, and hydroxyl ion.
Preferable 5 member ring or 6 member ring formed by Z1 and Z2 in the general formula representing the compound of the invention includes, thiazole ring (thiazole, 4-methylthiazole, 4-phenylthiazole, 4,5-diphenylthiazole, 4,5-dimethylthiazole); benzothiazole ring (benzothiazole, 5-methylbenzothiazole, 5-phenylbenzothiazole, 5-methoxybenzothiazole, 4-fluorobenzothiazole, 5,6-dioxymethylenebenzothiazole, 5-nitrobenzothiazole, 5-trifluoromethylbenzothiazole, 5-methoxycarbonylbenzothiazole, 6-hydroxybenzothiazole, 5-cyanobenzothiazole, 5-iodobenzothiazole); naphtothiazole ring (α-naphtothiazole, β-naphtothiazole, γ-naphtothiazole, 5-methoxy-β-naphtothiazole, 8-methoxy-α-naphtothiazole, 6-methoxy-8-acetoxy-β-naphtothiazole, 8,9-dihydroxy-β-naphtothiazole); oxazole ring (4-methyloxazol, 4-phenyloxazol, 4,5-diphenyloxazol, 4-phenoxyloxazol); benzoxazole ring (benzoxazole, 5-chlorobenzoxazole, 5,6-dimethylbenzoxazole, 6-hydroxybenzoxazole, 5-phenylbenzoxazole); naphtoxazole ring (α-naphtoxazole, β-naphtoxazole, γ-naphtoxazole); selenazole ring (for example, 4-methylselenazole, 4-phenylselenazole); benzselezole or benzselenazole ring (benzselenazole, 5-chlorobenzselenazole, 5,6-dimethylbenzselenazole, 6-hydroxybenzselenazole, 5-phenylbenzselenazole); thyazoline ring (thyazoline, 4,4-dimethylthyazoline); 2-pyridine ring (2-pyridine, 5-methyl-2-pyridine, 5-methoxy-2-pyridine, 4-chloro-2-pyridine, 5-carbamoyl-2-pyridine, 5-methoxycarbonyl-2-pyridine, 4-acetylamino-2-pyridine, 6-methylthio-2-pyridine, 6-methyl-2-pyridine); 4-pyridine ring (4-pyridine, 3-methoxy-4-pyridine, 3,5-dimethyl-4-pyridine, 3-chloro-4-pyridine, 3-methyl-4-pyridine); 2-quinoline ring (2-quinoline, 6-methyl-3-quinoline, 6-chloro-2-quinoline, 6-ethoxy-2-quinoline, 6-hydroxy-2-quinoline, 6-nitro-2-quinoline, 6-acetylamino-2-quinoline, 8-fluoro-2-quinoline); 4-quinoline ring (4-quinoline, 6-methoxy-4-quinoline, 6-acetylamino-4-quinoline, 8-chloro-4-quinoline, 8-trifluoromethyl-4-quinoline); 1-isoquinoline ring (1-isoquinoline, 6-methoxy-1-isoquinoline, 6-acetylamino-1-isoquinoline, 6-chloro-1-isoquinoline); 3,3-dialkylindolenine ring (3,3-dimethylindolenine, 3,3,7-trimethylindolenine, 5-chloro-3,3-dimethylindolenine, 5-ethoxycarbonyl-3,3-dimethylindolenine, 5-nitro-3,3-dimethylindolenine, 3,3-dimethyl-4,5-phenyleneindolenine, 3,3-dimethyl-6,7-phenyleneindolenine, 5-acetylamino-3,3,-diethylindolenine, 5-diethylamino-3,3-dipropylindolenine, 5-benzoylamino-3-ethyl-3-methylindolenine); imidazole ring (imidazole, 1-methyl-4-phenylimidazole, 1-benzil-4,5-dimethylimidazole); benzimidazole ring (benzimidazole, 1-methylbenzimidazole, 1-methyl-5-trifluoromethylbenzimidazole, 1-ethyl-5-chlorobenzimidazole, 1-phenyl-5-methoxycarbonylbenzimidazole, 1-ethyl-5-dimethylaminobenzimidazole); naphtoimidazole ring (1-methyl-α-naphtoimidazole, 1-methyl-5-methoxy-β-naphtoimidazole).
Typical compound used in the invention includes the following compounds. However, the invention is not limited to these compounds. Compounds represented by B-1 to B-42 and D-1 and D-2 are novel compounds. Therefore, the invention also relates to these novel compounds.
Chemical structures of the compounds of the invention are as follows. Compounds A-1 to A-22 are compounds represented by general formula (2). Compounds B-1 to B-42 are compounds represented by general formula (3) according to the invention. Compounds C-1 to C-12 are compounds represented by general formula (6) according to the invention. Compounds D-1 and D-2 are compounds represented by general formula (7) according to the invention.
Compounds represented by general formulae (9) and (10) are controls to those of the invention represented by general formulae (1) to (3), (6) and (7). Compounds S-1 to S-4 are compounds represented by general formula (9). Compounds S-5 to S-6 are compounds represented by general formula (10).
The pharmaceutical composition containing the above compounds can be used as an effective therapeutic and prophylactic agent against malaria, African trypanosomiasis (African sleeping sickness), American trypanosomiasis (Chagas disease), leishmania, babesiosis, lymphatic filariasis, toxoplasmosis (opportunistic infection caused by HIV infection), cryptospolidiosis (tropical diarrhea), and other various types of infections caused by parasitic protozoa.
The pharmaceutical composition of the invention may contain one or more compounds of the invention as active ingredients. Furthermore, the composition may be used in combination with other therapeutic agent known in the art including conventional anti-protozoa infection drugs. Preferable anti-protozoa infection drugs include chloroquine, mefloquine, artemisinin, atovaquone and pyrimethamine (therapeutic drug for malaria); suramin, pentamidine, melarsoprol, and ascofuranone (therapeutic drug for African sleeping sickness), benznidazole (therapeutic drug for chagas disease), pentostam, amphotericin B, miltefosine, and fluconazole (therapeutic drug for leishmaniasis).
Preferable pharmaceutical carrier or diluent which can be used for pharmaceutical composition of the invention in combination with the compound represented by general formula (1) includes; sodium chloride; magnesium chloride; zinc chloride; glucose; saccharose; lactose; ethyl alcohol; glycerin; mannitol; sorbitol; pentaerythritol; diethylene glycol, propylene glycol, dipropyrene glycol, polyethylene glycol 400, other polyethylene glycols; monotriglyceride, ditriglyceride, or triglyceride of fatty acid such as glyceryl trilaurate and glyceryl distearate; pectin; starch; arginine acid; xylose; talc; lycopodium; oil and fat such as olive oil, peanut oil, castor oil, corn oil, safflower oil, a wheat germ oil, sesame oil, cotton oil, sunflower seed oil and cod liver oil; gelatin; lecithin; silica; cellulose; cellulose derivatives such as methyl hydroxypropylcellulose, methylcellulose and hydroxyethyl cellulose; fatty acid salt having 12 to 22 carbon atoms such as calcium stearate, calcium laurate, magnesium oleatete, calcium palmitate, calcium behenate, magnesium stearate; cyclodextrin (α-cyclodextrin, β-cyclodextrin, γ-cyclodextrin, hydroxyethyl-β-cyclodextrin, hydroxypropyl-β-cyclodextrin, dihydroxypropyl-β-cyclodextrin, carboxymethylethyl-β-cyclodextrin, cycloawaodorin, dimethyl-β-cyclodextrin); emulsifier (saturated and unsaturated fatty acid having 2 to 22, particularly 10 to 18 carbon atoms; ester with monovalent aliphatic alcohol or multivalent alcohol having 1 to 20 carbon atoms such as glycol, glycerin, diethylene glycol, pentaerythritol, ethyl alcohol butyl alcohol, octadecyl alcohol; and silicone such as dimethylpolysiloxane. Other additional carrier which is conventionally used for pharmaceutical composition and known to those skilled in the art can be used for pharmaceutical composition of the invention, as well.
Pharmaceutically effective dose and administration method/route of the composition of the invention can be selected by those skilled in the art as appropriately depending on the species of the causative parasitic protozoa, site of the parasite, severity of the illness, therapeutic strategy, and patient's condition (age, weight, sex, general condition, and genetic ethnicity). Generally, 1 to 10,000 mg/day/70 kg, more generally 50 to 2000 mg/day/70 kg of the compound of the invention can be administered.
The pharmaceutical composition of the invention can be formulated into any form known to those skilled in the art depending on the administration method/route, and can be administrated accordingly. For example, the composition can be formulated into liquid, tablet, colloid medicine. Liquid medicine can be dissolved into 5% glucose aqueous solution, alternatively in combination with a carrier or dilution as above, and used for intravenous, intraperitoneal, or subcutaneous injection. Tablet medicine can be administered orally, and colloid medicine can be applied to skin. Appropriate amount of the compound represented by general formula (1) can be contained in the medicine depending on the purpose, subject who takes the medicine, and formulation of the pharmaceutical composition of the invention. Generally, the medicine may contain 1 mg to 10,000 mg, more preferably 10 mg to 3,000 mg compound of the invention.
Next, an example will be described for detailed illustration of the invention. Particularly, in order to clearly show the efficacy of the compound represented by general formulae (1) to (3), (6) and (7) used in the composition of the invention, proliferation inhibition activity was evaluated in in vitro screening test using malaria protozoa, leishmania protozoa, African trypanosoma protozoa, and American trypanosoma protozoa, and therapeutic effect was evaluated in in vivo study using malaria infected mouse. However, the technical field covered by the invention is not limited to these examples.
In this experiment, Plasmodium Falciparum k1 strain protozoa were used. The medium used in the experiment was filter-sterilized RPMI-1640 medium. To the medium human serum was added to achieve 5% concentration. The protozoa was cultured under condition of O2 concentration 3%, CO2 concentration 4%, N2 concentration 93%, and temperature 37° C.
Either the compound of the invention, control compounds (S-1 and S-3), and positive controls (Chloroquine) was dissolved into DMSO, to prepare test solutions having predefined concentration. The cultured malaria infected red blood cells were collected by centrifugation, diluted with non-infected red blood cells, to achieve initial infection rate 0.15%. The hematocrit was 2.5%.
To each well in a 96-well culture plate, 200 μL malaria infected culture was added, and either test solution containing test compound at predefined concentration or DMSO having no test compound was added. Each test solution was prepared in duplicate. After 48 hours culture under 37° C., hypoxanthine labeled with radioactive tritium (3H) of 0.5 μCi was added to each well. After culturing under same condition for 24 hours, the product was collected on a glass fiber filter and washed. The intensity of radiation was measured by Beta plate liquid scintillation counter (Wallac Inc.), to determine malaria protozoa infection rate in test compound samples and control samples.
Using the malaria protozoa infection rate, the proliferation inhibition rate was calculated according to the following equation to determine 50% proliferation inhibition concentration (EC50).
Proliferation inhibition rate(%)={1−(b−a)/(c−a)}×100
a: initial infection rate
b: infection rate of test compound solution
c: infection rate of the control
Rat-derived L6 cells (rat skeletal myoblast cell) were used for this test. The medium was prepared as follows: to RPMI 1640 medium, L-glutamine (200 mM) and fetal bovine serum was added to achieve concentration of 1%, 10%. The sample was cultured under CO2 concentration 5% and temperature 37° C. Either the composition of the invention or control was dissolved into DMSO, to prepare test solutions having predefined concentration.
The samples were precultured until logarithmic growth phase was reached. Then the culture was transferred to each well in a 96-well culture plate, and either test solution containing test compound at predefined concentration or DSMO without compound was added. The test solution was duplicated.
The plate was cultured in an incubator for 72 hours, to examine proliferation inhibition activity. The activity was examined as follows. Alamar Blue water solution 10 μL was added to each well, and culture was continued for 2 hours. Next, the culture plate was mounted on a fluorescence microplate reader (Spectramax Gemeni XS; Molecular Devices Corporation, U.S.), and irradiated with excitation wavelength 536 nm to determine fluorescence at 588 nm. The survival rate of L6 cells in the test solution sample and control sample was calculated.
Using the survival rate thus obtained, the proliferation inhibition rate against L6 cells was calculated according to the following equation to determine 50% proliferation inhibition concentration (EC50).
Proliferation inhibition rate(%)={(C−A)/(B−A)}×100
A: Initial cell count
B: Cell count in control after 3 days
C: Cell count in test solution after 3 days
Anti-malaria effect of the sample was evaluated based on the EC50 value of the sample for Chloroquine-resistant tropical malaria protozoa and rat L6 cells. Chemotherapeutic index, which is used as an indicator of selective toxicity against Chloroquine-resistant malaria protozoa, was calculated according to the following equation to determine effect of the test compound. The higher the selective toxicity value, the lower the adverse effect risk (side effects).
Chemotherapeutic index=(EC50 value of sample against rat L6 cells)/(EC50 value of sample against Chloroquine-resistant malaria protozoa)
The EC50 values and selective toxicity index of the compound of the invention and positive control against Chroloquine-resistant malaria protozoa and rat L6 cells are respectively shown in table 1.
P. falciparum K1
As clearly shown in the table, the compound of the invention showed proliferation inhibition effect equivalent or exceeding that of Chloquine (anti-malaria drug currently in clinical use) as a positive control, and that of control compound S-3 against malaria protozoa. Furthermore, some compounds of the invention showed high selective toxicity value as an adverse effect index. Based on these findings, it was determined that the compound of the invention is an effective therapeutic agent against malaria.
In this experiment, bloodstream form trypomastigote of Trypanosoma brucei rhodensiense (STIB 900 strain) was used. The medium used in the experiment was prepared as follows: to filter-sterilized MEM medium, 25 mM N-2-hydroxyethylpiperazine-2-ethane sulfonate (HEPES), 1 g/L glucose, 1% MEM nonessential amino acid, 0.2 mM 2-mercaptoethanol, 2 mM pyruvic calcium salt, 0.1 mM hypoxanthine, and 15% heat-treated horse serum were added. The protozoa was cultured under atmosphere of CO2 concentration 5% and temperature 37° C.
Either the compound of the invention or a positive control (melarsoprol) was dissolved into dimethylsulfoxide (DMSO) to prepare test solution having predefined concentration. To each well in a 96-well culture plate, medium containing 8×103 protozoa, and either test solution containing the test compound at predefined concentration or DMSO without compound was added. Then medium was added to achieve 100 μL. The test solution was duplicated.
The culture plate was cultured in an incubator for 72 hours, and the proliferation inhibition activity was examined. The activity was determined as follows. To each well, 10 μL Alamar blue water solution was added, then the plate was again cultured for 2 hours. Then the culture plate was mounted on a fluorescence microplate reader (Spectramax Gemeni XS; Molecular Devices Corporation, U.S.), and irradiated with 536 nm excitation wavelength to determine fluorescence at 588 nm. The trypanosoma infection rate of the sample containing the test composition and that of the control sample was calculated.
Using the protozoa infection rate thus obtained, the proliferation inhibition rate was calculated according to the following equation to determine 50% proliferation inhibition concentration (EC50).
Proliferation inhibition rate(%)={1−(b−a)/(c−a)}×100
a: initial infection rate
b: infection rate of the test compound solution
c: infection rate of the control
Selective toxicity index, which is used as an indicator of selective toxicity against African trypanosoma protozoa, was calculated according to the following equation to determine effect of the test composition.
Selective toxicity index=(EC50 value of sample against rat L6 cells)/(EC50 value of sample against African trypanosoma protozoa)
The EC50 values and selective toxicity index of the compound of the invention and positive control against African trypanosoma protozoa and rat L6 cells are respectively shown in table 2.
Trypanosoma brucei rhod.
As clearly shown in the table, the compound of the invention showed proliferation inhibition effect equivalent or exceeding that of melarsoprol (anti-African trypanosoma drug currently in clinical use) as a positive control, and that of control compound S-3 against African trypanosoma protozoa. Based on these findings, it was determined that the compound of the invention is an effective therapeutic agent against African trypanosoma (African sleeping sickness).
In this experiment, amastigote and trypomastigote of Trypanosoma cruzi (Tulahuen C2C4 strain) infected to rat L6 cells were used. The medium used in the experiment was prepared as follows: to RPMI 1640 medium containing L6 cells, L-glutamine (200 mM) and fetal bovine serum was added to achieve concentration of 1% and 10%, respectively. The culture was conducted under CO2 concentration 5% and temperature 37° C.
Either the compound of the invention or a positive control (benznidazole) was dissolved into DMSO to prepare test solution having predefined concentration. To each well in a 96-well culture plate, medium containing 5×103 protozoa was added and precultured for 48 hours. After replacing the medium, either the test solution containing compound of the invention in predefined concentration or DMSO without compound was added. The test solution was duplicated.
The plate was cultured in an incubator for 96 hours, and the proliferation inhibition activity was examined. The activity was determined as follows. To each well, 50 μL CPRG/Nonidet was added, then left for 2 to 6 hours. Then the culture plate was mounted on an absorption microplate reader to determine absorption at 540 nm. The trypanosoma infection rate of the sample containing the test compound and that of the control sample was calculated.
Using the protozoa infection rate thus obtained, the proliferation inhibition rate was calculated according to the following equation to determine 50% proliferation inhibition concentration (EC50).
Proliferation inhibition rate(%)={1−(b−a)/(c−a)}×100
a: initial infection rate
b: infection rate of the test compound solution
c: infection rate of the control
Selective toxicity index, which is used as an indicator of selective toxicity against American trypanosoma protozoa, was calculated according to the following equation to determine effect of the compound of the invention.
Selective toxicity index=(EC50 value of sample against rat L6 cells)/(EC50 value of sample against American trypanosoma protozoa)
The EC50 values and selective toxicity index of the compound of the invention and positive control against American trypanosoma protozoa and rat L6 cells are respectively shown in table 3.
Trypanosoma cruzi
As clearly shown in the table, the compound of the invention showed proliferation inhibition effect equivalent or exceeding that of benznidazole (anti-American trypanosoma (Chagas' disease) drug currently in clinical use) as a positive control, and that of control compound S-3 against American trypanosoma protozoa. Based on these findings, it was determined that the compound of the invention is an effective therapeutic agent against American trypanosoma (Chagas' disease).
In this experiment, Leishmania donovani (MHOM/ET/67/L82 strain) was used. The protozoa were successively cultured in Syrian Golden hamsters to obtain amastigote. The medium used in the experiment was SM medium having heat-treated fetal bovine serum 10% added, and pH prepared to 5.4. The culture was conducted under CO2 concentration 5% and temperature 37° C.
Either the compound of the invention or a positive control (miltefosine) was dissolved into DMSO to prepare test solution having predefined concentration. To each well of a 96-well culture plate, medium containing predetermined number of protozoa was added and the culture was pre-treated. The concentration of amastigote was determined by CASY cell analyze system (Scharfe GMBH Co., Germany). Subsequently, either test solution containing compound of the invention in predefined concentration or DMSO without compound was added. The test solution was duplicated.
The plate was cultured in an incubator for 72 hours, and the proliferation inhibition activity was examined. The activity was determined as follows. To each well, 10 μL Alamar blue aqueous solution was added, then cultured again for 2 hours. Then the culture plate was mounted on a fluorescence microplate reader (Spectramax Gemeni XS; Molecular Devices Corporation, U.S), and irradiated 536 nm excitation wavelength to determine absorption at 588 nm. The leishmania infection rate of the sample containing the test compound and that of the control sample was calculated.
Using the protozoa infection rate thus obtained, the proliferation inhibition rate was calculated according to the following equation to determine 50% proliferation inhibition concentration (EC50).
Proliferation inhibition rate(%)={1−(b−a)/(c−a)}×100
a: initial infection rate
b: infection rate of test compound solution
c: infection rate of the control
Selective toxicity index, which is used as an indicator of selective toxicity against leishmania, was calculated according to the following equation to determine the effect of the compound of the invention.
Selective toxicity index=(EC50 value of sample against rat L6 cells)/(EC50 value of sample against leishmania protozoa)
The EC50 values and selective toxicity indexes of the compound of the invention and positive control against leishmania protozoa and rat L6 cells are respectively shown in table 4.
Leishmania donovani
As clearly shown in the table, the compound of the invention showed proliferation inhibition effect equivalent or exceeding that of miltefosine (anti-leishmania (Chagas' disease) drug currently in clinical use) as a positive control, and that of control compound S-3 against leishmania protozoa. Based on these findings, it was determined that the compound of the invention is an effective therapeutic agent against leishmania.
For a test to evaluate therapeutic effect of the compound, 4-day suppressive test which is commonly used for in vivo test to evaluate activity of anti-malaria compound was used. In this experiment, rodent malaria protozoa (Plasmodium berghei NK 65 strain) were used. The infected blood was collected from 5-weeks age (SPF) ICR strain male mouse which were infected intraperitoneally and successively cultured. From the caudal vein of the infected mouse, blood was collected to calculate infection rate. After confirming that infection rate was adequately elevated (10% to 20% infection), the malaria infected blood was collected from the heart of the mouse. The infection rate and count of the red blood cells (cells/mL) were calculated. The infected red blood cell was diluted with PBS buffer to achieve 1.0×10−4 protozoa per 0.2 mL dose. The infected cells were injected to the caudal vein of uninfected mouse (ICR strain, male, 5-weeks age) to cause infection. Five mice were made into one group, and the test compound was administered in predefined concentration. From 2 hours after infection, the compound was administered every 24 hours for straight 4 days.
The compound of the invention to be used in this test was dissolved in saline (Otsuka Pharmaceutical Co., Ltd.) to obtain test solution of predefined concentration. When the compound was not dissolved in saline, it was dissolved in SSV (saline containing 0.5% sodium=carboxymethyl cellulose, 0.5% benzyl alcohol, 0.4% Tween 80) to prepare test solution. For the control group (non-treatment group), only saline (Otsuka) was administered. Positive controls S-1 to S-5 were dissolved in saline (Otsuka) or SSV in predetermined concentration to prepare test solution. When the compound was not dissolved in saline, it was dissolved in SSV. After measuring weight of each mouse, the dose for each mouse was calculated to achieve 5.0 to 40 mg concentration for weight1 kg.
Five mice were made into one group, and the test compound was administered intraperitoneally at predefined concentration. From 2 hours after infection, the compound was administered every 24 hours for straight 4 days. Subsequent to the 24 hours after last treatment, blood was collected from the tail of the mouse to prepare thin layer smear in order to count malaria protozoa infection in the treatment group and the control group under microscope. The mice showing maximum value and minimum value were excluded from the average calculation (average was calculated for three mice), to determine malaria protozoa infection rate (Parasitemia).
Using malaria protozoa infection rate thus calculated, recovery rate obtained from the test compound (suppression) was determined.
Recovery rate: suppression(%)=(b−a)/b×100
a: Protozoa infection rate in the treatment group
b: Protozoa infection rate in the control group
Mean survival days: MSD(day)=c−d
c: Average days from the initial treatment (date of malaria infection) to the date of death for the treatment group (5 mice)
d: Average days from the date of malaria infection to the date of death for the non-treatment (control) group (5 mice)
Condition of treated mice, such as change in weight and fur, was observed to evaluate adverse effect including acute toxicity of the drug. Tables 5 to 7 illustrate the recovery rate (%) and survival days (day) of malaria infected mice treated with intraperitoneal injection of the test compound and the control compound at predefined concentration. The meaning of symbols in the table is as follows.
* ND: Survival day was not calculated
** All: mice died during treatment period due to acute toxicity of the drug.
As clearly shown in the above tables, the compound of the invention improved recovery rate of malaria and significantly prolonged survival compared to S-1 to S-6 compounds as controls. Thus, the compound is an effective therapeutic agent against malaria. Compared to Chloroquine which is currently in clinical use, the compound of the invention shows equivalent or exceeding recovery rate. The control compounds S-2 and S-4 had such high toxicity that it caused death at 25 mg/kg/day dose due to acute toxicity. On the contrary, many compounds of the invention showed no acute toxicity at 25 mg/kg/day dose. Therefore, the compound of the invention is an effective therapeutic agent against malaria with improved adverse effect profile.
3-ethyl-5-(1-methyl-1H-quinoline-2-ylidene)-2-methylsulfanil-4-oxo-4,5-dihydro-3-thiazolium-β-toluenesulfonate 244 mg and 2-amino-1-methylpyridinium=p-toluenesulfonate 140 mg were dissolved into 2.5 mL acetonitrile. To the solution, 0.21 mL triethylamine was agitatedly titrated at 70° C. The agitation was continued for 6 hours at same temperature. To the mixture, 2.5 mL ethyl acetate was added at 70° C., and the mixture was cooled to ambient temperature and left for 30 minutes. The crystal was sucked, filtered, and washed with acetonitrile-ethyl acetate mixture (1:1 v/v). The resultant coarse crystal was dissolved into chloroform-methanol mixture solution (1:1 v/v), then introduced into a column filled with strong base ion-exchange resin (Amberite IRA-400, Sigma-Aldrich Japan K.K.) to elute with chloroform-methanol mixture solution (1:1 v/v). The elusion was concentrated under reduced pressure to obtain solid substance. The solid was recrystallized using methanol-ethyl acetate mixture to obtain the intended compound.
yield 147 mg (71%), melting point 239-240° C.
A mixture of methylsulfanylpyridinium=p-toluensulfonate 7.79 g and 3-ethyl-2thioxothiazolidine-4-on 4.03 g was dissolved in 25 mL acetonitrile and cooled to 0° C. To the solution, triethylamine 10.5 mL was agitatedly titrated at 0° C.
The reaction temperature was raised to 10° C., and agitation was continued for 4 hours.
The resultant crystal was sucked, filtered, washed with acetonitrile, and dried under reduced pressure to obtain intended compound.
yield 5.37 g (85% yield), melting point 148-150° C.
The mixture of 3-ethyl-5-(1-methyl-1H-piridine-2-ylidene)-2-thioxothiazolidine-4-on 5.06 g and p-toluenesulfonate methyl 11.2 g was heated to 130° C. and agitated for 4 hours. The mixture was cooled to ambient temperature, and added with 20 mL ethyl acetate and agitated for 30 minutes. The resultant crystal was sucked, filtered, washed with ethyl acetate, and dried under reduced pressure at ambient temperature to obtain intended compound.
yield 8.45 g (96%), melting point 156 to 158° C.
The mixture of 2-amino-6-chloro-3-methyl-3-benzothiazolium=p-toluensulfonate 1.74 g and ethylisothyocianate 0.42 mL was dissolved in 2.5 mL pyridine. To the solution, 0.66 mL triethylamine was titrated at ambient temperature, then the resultant solution was heated to 110° C., and agitated for 45 minutes. Ice water was added to the mixture. The resultant precipitate was sucked, filtered and washed with distilled water, then dried under reduced pressure. To the resultant coarse product, bromoacetic acid 1.29 g and acetic acid 4 mL were added, and the mixture was agitated at 90° C. for 30 minutes. After cooling to the ambient temperature, the mixture was added with 10 mL diethyl ether and left for 30 minutes. The resultant crystal was sucked, filtered, washed with diethyl ether, and dried under reduced pressure. The resultant coarse crystal was recrystallized using methanol to obtain the intended compound.
yield 1.72 g (90%), melting point 233-235° C.
6-chloro-2-(3-ethyl-4-oxothiazolidine-2-ylideneamino)-3-methyl-3-benzothiazolium=bromide 203 mg and 3-ethyl-5-(1-methyl-1H-pyridine-2-ylidene)-2-methylsulfanyl-4-oxo-4,5-dihydro-3-thiazolium=p-toluenesulfonate 182 mg was dissolved in acetonitrile 5 mL. To the solution, triethylamine 0.21 mL was titrated at ambient temperature, then the resultant solution was agitated at 70° C. for 15 hours. The mixture was cooled to ambient temperature then the resultant precipitate was sucked, filtered, and washed with acetonitrile. The resultant coarse crystal was dissolved in chloroform-methanol mixed solution (1:1 v/v), and introduced through a column filled with strong base ion exchange resin (Amberlite IRA-400 by Aldrich), then eluted with chloroform-methanol mixture (1:1 v/v). The elution was concentrated under reduced pressure to obtain solid. The solid was recrystallized using methanol-ethyl acetate mixture to obtain the intended compound.
yield 186 mg (77%), melting point 203-205° C. (decomp.)
2-amino-4-(4-chlorophenyl) thiazole 500 mg and p-toluenesulfonate methyl 0.39 mL was dissolved in acetonitrile 0.59 mL, and agitated at 80° C. for 20 hours. The mixture was cooled to ambient temperature. The resultant precipitate was sucked, filtered and washed with ethyl acetate, then dried under reduced pressure to obtain the intended compound.
yield 704 mg (75%)
2-amino-4-(4-chlorophenyl)-3-methyl-3-thiazolium=p-toluenesulfonate 76 mg and 3-ethyl-5-(2-(3-methyl-3H-benzothiazole-2-ylidene)ethylidene)-2-methylsulfanyl-4-oxo-4,5-dihydro-3-thiazolium=p-toluene sulfonate 100 mg was dissolved in acetonitrile 6.4 mL. To the solution, triethylamine was titrated at ambient temperature 0.077 mL, then the resultant solution was agitated at 70° C. for 5.5 hours. The mixture was cooled to ambient temperature, and the resultant precipitate was sucked, filtered and washed with acetonitrile. The obtained coarse crystal was dissolved in chloroform-methanol mixture (1:1 v/v), then introduced through a column filled with strong base ionexchange resin (Amberlite IRA-400 by Aldrich). The resultant product was eluted by chloroform-methanol mixture (1:1 v/v). The elution was concentrated under reduced pressure to obtain solid. The solid was recrystallized by methanol-ethyl acetate mixture to obtain the intended compound.
yield 47 mg (44%)
Other compounds of the invention were synthesized using methods similar to the above. The spectrum data of each compound of the present invention is as follows:
A-1 Mp 263-265° C. (decomp.); IR (KBr) 1647, 1535, 1489, 1416, 1352 cm−1; 1H NMR (DMSO-d6) δ 8.37 (1H, d, J=2.2 Hz), 8.05 (1H, d, J=8.3 Hz), 8.02 (1H, d, J=9.0 Hz), 7.86-7.81 (2H, m), 7.59 (1H, dd, J=7.3, 8.3 Hz), 7.42 (1H, dd, J=7.6, 7.6 Hz), 4.27-4.02 (5H, m), 4.02 (3H, s), 1.35 (3H, t, J=7.1 Hz); MS (FAB) m/z 473 (M+).
A-2 mp 291-293° C. (decomp.); IR (KBr) 1653, 1609, 1531, 1479, 1394, 1167 cm−1; 1H NMR (DMSO-d6) δ 8.38 (1H, s), 8.34 (1H, d, J=9.0 Hz), 8.22 (1H, d, J=7.3 Hz), 8.08 (1H, d, J=8.8 Hz), 8.01 (1H, d, J=8.1 Hz), 7.98 (1H, d, J=9.0 Hz), 7.92 (1H, dd, J=7.6, 8.1 Hz), 7.81 (1H, d, J=8.8 Hz), 7.65 (1H, dd, J=7.3, 7.6 Hz), 4.22-4.13 (5H, m), 4.01 (3H, s), 1.35 (3H, t, J=7.1 Hz); MS (FAB+) m/z 467 (M+).
A-4 mp 232-234° C. (decomp.); IR (KBr) 1641, 1524, 1497, 1445, 1375, 1281 cm−1; 1H NMR (DMSO-d6) 8.49 (1H, d, J=6.6 Hz), 8.42 (1H, d, J=8.3 Hz), 8.33 (1H, s), 8.04 (1H, dd, J=7.1, 8.3 Hz), 7.92 (1H, d, J=8.8 Hz), 7.77 (1H, d, J=8.8 Hz), 7.34 (1H, dd, J=6.6, 7.1 Hz), 4.26 (3H, s), 4.17 (2H, q, J=7.1 Hz), 3.96 (3H, s), 1.32 (3H, t, J=7.1 Hz); MS (FAB) m/z 417 (M+).
A-14 mp 239-240° C. (decomp.); IR (KBr) 1612, 1508, 1481, 1394, 1165 cm−1; 1H NMR (DMSO-d6) δ 8.74 (1H, d, J=6.3 Hz), 8.33 (1H, dd, J=8.1, 8.1 Hz), 7.98 (1H, d, J=9.3 Hz), 7.90 (1H, d, J=8.5 Hz), 7.86-7.72 (4H, m), 7.47 (2H, dd, J=6.3, 8.1 Hz), 4.04 (3H, s), 4.01 (2H, q, J=7.1 Hz), 3.94 (3H, s), 1.29 (3H, t, J=7.1 Hz); MS (FAB+) m/z 377 (M+).
A-15 mp 262-264° C. (decomp.); IR (KBr) 1614, 1541, 1487, 1435, 1367, 1198 cm−1; 1H NMR (DMSO-d6) 8.85 (1H, d, J=7.3 Hz), 8.68 (1H, d, J=9.0 Hz), 8.49 (1H, d, J=8.8 Hz), 8.31 (1H, s), 8.22 (1H, d, J=6.6 Hz), 7.88 (1H, d, J=9.0 Hz), 7.81 (1H, dd, J=6.8, 8.8 Hz), 7.59 (1H, d, J=7.3 Hz), 7.05 (1H, dd, J=6.6, 6.8 Hz), 4.27 (3H, s), 4.19-4.06 (5H, m), 1.32 (3H, t, J=7.1 Hz); MS (FAB) m/z 411 (M+).
A-16 mp 267-269° C. (decomp.); IR (KBr) 1649, 1558, 1493, 1418, 1202 cm−1; 1H NMR (DMSO-d6) δ 9.08 (1H, d, J=6.8 Hz), 8.59 (1H, d, J=9.0 Hz), 8.46 (1H, s), 7.96 (1H, d, J=9.0 Hz), 7.92 (1H, d, J=7.8 Hz), 7.76 (1H, d, J=6.8 Hz), 7.62 (1H, d, J=8.3 Hz), 7.51 (1H, dd, J=7.3, 7.8 Hz), 7.33 (1H, dd, J=7.3, 8.3 Hz), 4.39 (3H, s), 4.15 (2H, q, J=7.1 Hz), 3.95 (3H, s), 1.36 (3H, t, J=7.1 Hz); MS (FAB) m/z 467 (M+).
A-17 mp>250° C. (decomp.); IR (KBr) 1636, 1539, 1489, 1407, 1350 cm−1; 1H NMR (DMSO-d6) δ 8.36 (1H, d, J=2.2 Hz), 8.09-8.00 (3H, m), 7.84 (1H, dd, J=2.2, 9.0 Hz), 7.49 (1H, dd, J=1.7, 8.3 Hz), 4.22 (2H, q, J=7.1 Hz), 4.18 (3H, s), 4.03 (3H, s), 1.35 (3H, t, J=7.1 Hz); MS (FAB) m/z 507 (M+).
A-19 1H NMR (DMSO-d6) 8.64 (1H, d, J=6.3 Hz), 8.24 (1H, t, J=7.6 Hz), 8.05 (1H, d, J=6.5 Hz), 7.92 (1H, d, J=6.3 Hz), 7.90 (1H, d, J=7.2 Hz), 7.34 (1H, dd, J=6.5, 7.2 Hz), 7.09 (1H, dd, J=7.6, 7.2 Hz), 4.11 (3H, s), 4.03 (2H, q, J=7.0 Hz), 4.00 (3H, s), 1.23 (3H, t, J=7.0 Hz); MS (FAB) m/z 368 (M+).
B-2 mp 203-205° C. (decomp.); IR (KBr) 1636, 1541, 1489, 1373, 1271, 1005 cm−1; 1H NMR (DMSO-d6) 8.44 (1H, d, J=8.78 Hz), 8.37 (1H, d, J=2.20 Hz), 8.29 (1H, d, J=6.59 Hz), 7.98 (1H, d, J=8.78 Hz), 7.85 (1H, dd, J=6.83, 8.78 Hz), 7.80 (1H, dd, J=2.20, 8.78 Hz), 7.10 (1H, dd, J=6.59, 6.83 Hz), 4.26-4.15 (7H, m), 4.00 (3H, s), 1.46-1.25 (6H, m); MS (FAB) m/z 544 (M+).
B-3 mp>250° C. (decomp.); IR (KBr) 1636, 1578, 1489, 1435, 1366, 1155 cm−1; 1H NMR (DMSO-d6) 9.06 (1H, d, J=2.4 Hz), 8.46-8.46 (2H, m), 8.15 (1H, d, J=6.1 Hz), 7.89 (1H, d, J=9.3 Hz), 7.73 (1H, dd, J=6.8, 8.5 Hz), 6.97 (1H, dd, J=6.1, 6.8 Hz), 4.11 (3H, s), 4.09-3.97 (7H, m), 1.29-1.20 (6H, m); MS (FAB) m/z 488 (M+).
B-4 mp>300° C. (decomp.); IR (KBr) 1653, 1616, 1483, 1435, 1396, 173 cm−1; 1H NMR (DMSO-d6) 8.81 (1H, d, J=6.3 Hz), 8.39 (1H, dd, J=7.2, 8.7 Hz), 7.98-7.85 (2H, m), 7.84-7.70 (4H, m), 7.54 (1H, dd, J=6.3, 7.2 Hz), 7.44 (1H, dd, J=7.2, 7.5 Hz), 4.06 (3H, s), 4.04-3.97 (4H, m), 3.95 (3H, s), 1.28 (3H, t, J=7.0 Hz), 1.24 (3H, t, J=7.0 Hz); MS (FAB) m/z 504 (M+).
B-5 mp>300° C. (decomp.); IR (KBr) 1624, 1541, 1489, 1437, 1375, 1155 cm−1; 1H NMR (DMSO-d6) 8.66 (1H, d, J=6.6 Hz), 8.45 (1H, d, J=8.5 Hz), 8.34 (1H, dd, J=7.3, 8.5 Hz), 8.12 (1H, d, J=7.3 Hz), 7.89 (1H, d, J=8.3 Hz), 7.70 (1H, dd, J=7.3, 7.3 Hz), 7.60-7.45 (6H, m), 6.94 (1H, dd, J=6.6, 6.6 Hz), 4.08 (5H, m), 3.76 (3H, s), 1.27 (3H, t, J=7.1 Hz); MS (FAB) m/z 502 (M+).
B-6 mp 258-260° C. (decomp.); IR (KBr) 1624, 1541, 1491, 1437, 1373, 1155 cm−1; 1H NMR (DMSO-d6) 8.73 (1H, d, J=6.3 Hz), 8.44 (1H, d, J=8.3 Hz), 8.35 (1H, dd, J=7.1, 7.1 Hz), 8.14 (1H, d, J=6.6 Hz), 7.88 (1H, d, J=7.8 Hz), 7.71 (1H, dd, J=7.1, 7.1 Hz), 7.48 (1H, dd, J=6.3, 7.8 Hz), 6.95 (1H, dd, J=6.6, 8.3 Hz), 4.11 (3H, s), 4.08-3.97 (7H, m), 1.27 (3H, t, J=7.1 Hz), 1.23 (3H, t, J=7.1 Hz); MS (FAB) m/z 454 (M+).
B-8 mp>250° C. (decomp.); IR (KBr) 1636, 1541, 1487, 1435, 1373, 1153 cm−1; 1H NMR (DMSO-d6) 8.45 (1H, d, J=8.54 Hz), 8.26 (1H, d, J=6.59 Hz), 7.83 (1H, dd, J=7.32, 8.54 Hz), 7.77 (1H, s), 7.71-7.64 (4H, m), 7.09 (1H, dd, J=6.59, 7.32 Hz), 4.22 (2H, q, J=7.07 Hz), 4.16 (3H, s), 4.13 (2H, q, J=7.32 Hz), 3.71 (3H, s), 1.38-1.28 (6H, m); MS (FAB) m/z 570 (M+);
B-11 mp>300° C. (decomp.); IR (KBr) 1636, 1541, 1487, 1437, 1373, 1161 cm−1; 1H NMR (DMSO-d6) 8.45 (1H, d, J=8.8 Hz), 8.37 (1H, d, J=2.2 Hz), 8.29 (1H, d, J=6.6 Hz), 7.92-7.83 (2H, m), 7.78 (1H, dd, J=2.2, 8.8 Hz), 7.66-7.52 (5H, m), 7.12 (1H, dd, J=6.6, 7.1 Hz), 4.30 (2H, q, J=7.1 Hz), 4.16 (3H, s), 3.61 (3H, s), 1.42 (3H, t, J=7.1 Hz); MS (FAB) m/z 592 (M+).
B-12 mp>300° C. (decomp.); IR (KBr) 1661, 1537, 1489, 1385, 1001 cm−1; 1H NMR (DMSO-d6) 8.39 (1H, d, J=2.2 Hz), 8.03 (1H, d, J=8.8 Hz), 7.83 (1H, dd, J=2.2, 8.8 Hz), 4.21-4.12 (4H, m), 4.02 (3H, s), 3.96 (2H, t, J=7.6 Hz), 3.48 (3H, s), 3.27 (2H, t, J=7.6 Hz), 1.32 (3H, t, J=7.3 Hz); MS (FAB) m/z 552 (M+).
B-14 mp>300° C. (decomp.); IR (KBr) 1653, 1609, 1543, 1475, 1389, 1161 cm−1; 1H NMR (DMSO-d6) 8.35 (1H, d, J=2.2 Hz), 8.06 (1H, d, J=9.5 Hz), 7.92-7.87 (2H, m), 7.86-7.76 (3H, m), 7.69-7.58 (6H, m), 7.50 (1H, dd, J=7.0, 7.3 Hz), 4.28 (2H, q, J=7.3 Hz), 4.03 (3H, s), 3.63 (3H, s), 1.43 (3H, t, J=7.3 Hz); MS (FAB) m/z 642 (M+).
B-15 mp>300° C. (decomp.); IR (KBr) 1653, 1609, 1541, 1477, 1394 cm−1; 1H NMR (DMSO-d6) 8.34 (1H, d, J=2.2 Hz), 8.07 (1H, d, J=9.8 Hz), 8.00 (1H, d, J=9.0 Hz), 7.93-7.76 (5H, m), 7.49 (1H, dd, J=7.3, 7.6 Hz), 4.27-4.15 (4H, m), 4.04 (3H, s), 4.02 (3H, s), 1.43-1.31 (6H, m); MS (FAB) m/z 594 (M+).
B-16 mp 207-208° C. (decomp.); IR (KBr) 1636, 1528, 1487, 1437, 1373, 1155 cm−1; 1H NMR (DMSO-d6) 8.45 (1H, d, J=8.8 Hz), 8.36 (1H, d, J=2.2 Hz), 8.31 (1H, d, J=6.8 Hz), 7.97 (1H, d, J=9.0 Hz), 7.86 (1H, dd, J=6.8, 8.8 Hz), 7.79 (1H, d, J=9.0 Hz), 7.49 (2H, d, J=7.1 Hz), 7.41-7.28 (3H, m), 7.13 (1H, dd, J=6.8, 6.8 Hz), 5.34 (2H, s), 4.25 (2H, q, J=7.3 Hz), 4.18 (3H, s), 3.96 (3H, s), 1.36 (3H, t, J=7.3 Hz); MS (FAB) m/z 606 (M+);
B-17 mp>300° C. (decomp.); IR (KBr) 1638, 1541, 1485, 1439, 1373, 1165 cm−1; 1H NMR (DMSO-d6) 8.46 (1H, d, J=8.9 Hz), 8.37 (1H, d, J=1.5 Hz), 8.28 (1H, d, J=6.5 Hz), 7.91-7.82 (3H, m), 7.78 (1H, dd, J=1.5, 8.9 Hz), 7.49 (2H, d, J=8.9 Hz), 7.16 (2H, d, J=8.7 Hz), 7.11 (1H, t, J=6.5 Hz), 4.30 (2H, q, J=7.2 Hz), 4.16 (3H, s), 3.86 (3H, s), 3.64 (3H, s), 1.41 (3H, dd, J=6.5, 7.2 Hz); MS (FAB) m/z 622 (M+).
B-19 mp 252-253° C. (decomp.); IR (KBr) 1645, 1545, 1489, 1439, 1375, 1163 cm−1; 1H NMR (DMSO-d6) 8.44 (1H, d, J=8.8 Hz), 8.25 (1H, d, J=6.3 Hz), 8.00 (1H, d, J=4.4 Hz), 7.82 (1H, dd, J=7.3, 8.8 Hz), 7.75 (1H, d, J=4.4 Hz), 7.07 (1H, dd, J=6.3, 7.3 Hz), 6.01-5.89 (1H, m), 5.32-5.21 (2H, m), 4.67 (2H, d, J=5.4 Hz), 4.20 (2H, q, J=7.3 Hz), 4.15 (3H, s), 3.86 (3H, s), 1.33 (3H, t, J=7.3 Hz); MS (FAB) m/z 472 (M+).
B-20 1H NMR (DMSO-d6) 8.13 (1H, d, J=6.7 Hz), 8.04 (1H, dd, J=4.2, 7.6 Hz), 7.77 (1H, d, J=4.2 Hz), 7.20 (1H, dd, J=6.7, 7.6 Hz), 4.14-4.08 (7H, n, J=6.5, 7.2 Hz), 3.91 (3H, s), 1.31 (6H, m); MS (FAB) m/z 501 (M+).
B-21 mp 233-234° C. (decomp.); IR (KBr) 1638, 1541, 1489, 1437, 1375, 1157 cm−1; 1H NMR (DMSO-d6) 8.46 (1H, d, J=8.9 Hz), 8.27 (1H, d, J=6.5 Hz), 8.01 (1H, d, J=4.4 Hz), 7.83 (1H, dd, J=7.2, 8.9 Hz), 7.75 (1H, d, J=4.4 Hz), 7.46 (2H, d, J=7.2 Hz), 7.41-7.28 (3H, m), 7.09 (1H, dd, J=6.5, 7.2 Hz), 5.26 (2H, s), 4.20 (2H, q, J=7.0 Hz), 4.16 (3H, s), 3.85 (3H, s), 1.33 (3H, t, J=7.0 Hz); MS (FAB) m/z 522 (M+).
B-22 1H NMR (DMSO-d6) 8.12 (1H, d, J=6.2 Hz), 7.99 (1H, d, J=4.2, Hz), 7.75 (1H, dd, J=4.2, 2.1 Hz), 7.47 (2H, d, J=7.6 Hz), 7.36 (2H, dt, J=1.4, 7.6 Hz), 7.31 (1H, t, J=7.3 Hz), 7.19 (1H, t, J=6.2 Hz), 5.24 (s, 2H), 4.12 (2H, q, J=6.8 Hz), 4.06 (3H, s), 3.82 (s, 3H), 1.31 (3H, t, J=6.8 Hz); MS (FAB) m/z 563 (M+).
B-23 mp 200-202° C. (decomp.); 1H NMR (DMSO-d6) 8.04 (1H, d, J=4.4 Hz), 7.81 (1H, d, J=4.4 Hz), 7.45 (2H, d, J=7.1 Hz), 7.39-7.28 (3H, m), 5.23 (2H, s), 4.13 (2H, q, J=7.1 Hz), 3.94 (2H, t, J=7.6 Hz), 3.86 (3H, s), 3.47 (3H, s), 3.25 (2H, t, J=7.6 Hz), 1.29 (3H, t, J=7.1 Hz); MS (FAB) m/z 530 (M+).
B-24 mp>280° C. (decomp.); 1H NMR (DMSO-d6) δ 8.00 (1H, d, J=4.4 Hz), 7.82 (1H, d, J=4.4 Hz), 7.62-7.51 (5H, m), 4.17 (2H, q, J=7.3 Hz), 3.92 (2H, t, J=7.8 Hz), 3.52 (3H, s), 3.43 (3H, s), 3.25 (2H, t, J=7.8 Hz), 1.34 (3H, t, J=7.3 Hz); MS (FAB) m/z 516 (M+).
B-25 mp>250° C. (decomp.); IR (KBr) 1655, 1545, 1497, 1389, 1167 cm−1; 1H NMR (DMSO-d6) 8.00 (1H, d, J=4.4 Hz), 7.82 (1H, d, J=4.4 Hz), 7.44 (2H, d, J=8.8 Hz), 7.11 (2H, d, J=8.8 Hz), 4.16 (2H, q, J=7.1 Hz), 3.92 (2H, t, J=7.6 Hz), 3.84 (3H, s), 3.55 (3H, s), 3.42 (3H, s), 3.24 (2H, t, J=7.6 Hz), 1.33 (3H, t, J=7.1 Hz); MS (FAB) m/z 546 (M+).
B-26 mp>300° C. (decomp.); IR (KBr) 1653, 1541, 1491, 1389, 1167 cm−1; 1H NMR (DMSO-d6) 8.39 (1H, d, J=2.2 Hz), 7.91 (1H, d, J=8.8 Hz), 7.79 (1H, dd, J=2.2, 8.8 Hz), 7.48 (2H, d, J=8.8 Hz), 7.15 (2H, d, J=8.8 Hz), 4.21 (2H, q, J=7.3 Hz), 3.94 (2H, t, J=7.6 Hz), 3.85 (3H, s), 3.66 (3H, s), 3.45 (3H, s), 3.26 (2H, t, J=7.6 Hz), 1.37 (3H, t, J=7.3 Hz); MS (FAB) m/z 630 (M+).
B-27 mp 215-217° C. (decomp.); IR (KBr) 1653, 1541, 1504, 1389, 1194 cm−1; 1H NMR (DMSO-d6) 8.07 (1H, d, J=4.4 Hz), 7.82 (1H, d, J=4.4 Hz), 4.14-4.04 (4H, m), 3.93 (2H, t, J=7.6 Hz), 3.89 (3H, s), 3.46 (3H, s), 3.25 (2H, t, J=7.6 Hz), 1.28 (6H, t, J=7.3 Hz); MS (FAB) m/z 468 (M+).
B-28 mp>300° C. (decomp.); IR (KBr) 1636, 1481, 1435, 1373, 1232, 1151 cm−1; 1H NMR (DMSO-d6) 8.45 (1H, d, J=8.7 Hz), 8.27 (1H, d, J=6.8 Hz), 7.91 (1H, d, J=9.2 Hz), 7.89 (1H, d, J=2.7 Hz), 7.84 (1H, dd, J=6.8, 8.7 Hz), 7.35 (1H, dd, J=2.7, 9.2 Hz), 7.09 (1H, dd, J=6.8, 6.8 Hz), 4.29-4.12 (7H, m), 4.01 (3H, s), 3.87 (3H, s), 1.40-1.30 (6H, m); MS (FAB) m/z 540 (M+).
B-29 mp 202-204° C. (decomp.); 1H NMR (DMSO-d6) 7.95 (1H, d, J=9.0 Hz), 7.89 (1H, d, J=2.7 Hz), 7.36 (1H, dd, J=2.7, 9.0 Hz), 4.13 (4H, q, J=7.1 Hz), 4.02 (3H, s), 3.92 (2H, t, J=7.8 Hz), 3.87 (3H, s), 3.46 (3H, s), 3.25 (2H, t, J=7.8 Hz), 1.32 (6H, t, J=7.1 Hz); MS (FAB) m/z 548 (M+).
B-30 mp>300° C. (decomp.); IR (KBr) 1636, 1541, 1489, 1367, 1163, 1007 cm−1; 1H NMR (DMSO-d6) 8.45 (1H, d, J=8.7 Hz), 8.28-8.23 (2H, m), 7.97 (1H, d, J=8.3 Hz), 7.84 (1H, dd, J=7.3, 8.7 Hz), 7.75 (1H, dd, J=6.9, 8.3 Hz), 7.58 (1H, dd, J=6.9, 7.3 Hz), 7.08 (1H, t, J=6.4, 7.3 Hz), 4.28-4.14 (7H, m), 4.03 (3H, s), 1.42-1.30 (6H, m); MS (FAB) m/z 510 (M+).
B-31 mp 235-236° C. (decomp.); IR (KBr) 1653, 1543, 1489, 1364, 1192 cm−1; 1H NMR (DMSO-d6) 8.29 (1H, d, J=8.3 Hz), 8.02 (1H, d, J=8.7 Hz), 7.77 (1H, dd, J=7.8, 8.3 Hz), 7.62 (1H, dd, J=7.8, 8.3 Hz), 4.19-4.10 (4H, m), 4.05 (3H, s), 3.90 (2H, t, J=7.3 Hz), 3.46 (3H, s), 3.23 (2H, t, J=7.3 Hz), 1.36-1.29 (6H, m); MS (FAB) m/z 518 (M+).
B-32 mp>300° C. (decomp.); IR (KBr) 1636, 1541, 1477, 1437, 1371, 1153 cm−1; 1H NMR (DMSO-d6) 8.44 (1H, d, J=9.0 Hz), 8.28 (1H, d, J=6.3 Hz), 8.17 (1H, dd, J=2.9, 8.1 Hz), 8.01 (1H, dd, J=9.0, 9.3 Hz), 7.85 (1H, dd, J=6.8, 9.0 Hz), 7.66 (1H, dd, J=2.7, 9.0 Hz), 7.10 (1H, dd, J=6.3, 6.8 Hz), 4.30-4.12 (7H, m), 4.01 (3H, s), 1.41-1.30 (6H, m); MS (FAB) m/z 528 (M+).
B-33 mp>250° C. (decomp.); IR (KBr) 1655, 1541, 1489, 1362, 1209, 1001 cm−1; 1H NMR (DMSO-d6) 8.20 (1H, d, J=2.9, 8.1 Hz), 8.06 (1H, dd, J=9.0, 9.3 Hz), 7.69 (1H, dd, J=2.9, 9.0 Hz), 4.20-4.10 (4H, m), 4.03 (3H, s), 3.95 (2H, t, J=7.6 Hz), 3.48 (3H, s), 3.27 (2H, t, J=7.6 Hz); 1.32 (6H, t, J=7.1 Hz); MS (FAB) m/z 536 (M+).
B-34 mp 299-300° C. (decomp.); IR (KBr) 1645, 1541, 1489, 1437, 1377, 1163 cm−1; 1H NMR (DMSO-d6) 8.45 (1H, d, J=8.7 Hz), 8.26 (1H, d, J=6.9 Hz), 8.03 (1H, d, J=4.6 Hz), 7.82 (1H, dd, J=7.3, 8.7 Hz), 7.75 (1H, d, J=4.6 Hz), 7.07 (1H, dd, J=6.9, 7.3 Hz), 5.16-5.09 (1H, m), 4.20 (2H, q, J=6.9 Hz), 4.16 (3H, s), 3.89 (3H, s), 1.58 (6H, d, J=6.9 Hz), 1.33 (3H, t, J=6.9 Hz); MS (FAB) m/z 474 (M+).
B-35 mp>250° C. (decomp.); IR (KBr) 1655, 1541, 1500, 1391, 1170 cm−1; 1H NMR (DMSO-d6) δ 8.13 (1H, d, J=4.6 Hz), 7.86 (1H, d, J=4.6 Hz), 5.13-5.05 (1H, m), 4.08 (2H, q, J=7.3 Hz), 4.00-3.90 (5H, m), 3.47 (3H, s), 3.25 (3H, s), 1.57 (6H, d, J=6.9 Hz), 1.29 (3H, t, J=7.3 Hz); MS (FAB) m/z 482 (M+).
B-36 mp>300° C.; 1H NMR (DMSO-d6) 8.45 (1H, d, J=8.8 Hz), 8.38 (1H, d, J=2.2 Hz), 8.30 (1H, d, J=6.3 Hz), 7.99 (1H, d, J=8.8 Hz), 7.86 (1H, dd, J=7.1, 8.8 Hz), 7.81 (1H, dd, J=2.2, 8.8 Hz), 7.11 (1H, dd, J=6.3, 7.1 Hz), 5.26-5.17 (1H, m), 4.23 (2H, q, J=7.1 Hz), 4.18 (3H, s), 4.00 (3H, s), 1.61 (6H, d, J=6.8 Hz), 1.36 (3H, t, J=7.1 Hz); MS (FAB) m/z 558 (M+).
B-37 mp>300° C. (decomp.); IR (KBr) 1649, 1531, 1493, 1410, 1381, 1169 cm−1; 1H NMR (DMSO-d6) 8.40 (1H, d, J=2.2 Hz), 8.03 (1H, d, J=9.0 Hz), 7.83 (1H, dd, J=2.2, 9.0 Hz), 5.22-5.15 (1H, m), 4.16 (2H, q, J=7.3 Hz), 4.02 (3H, s), 3.96 (2H, t, J=7.8 Hz), 3.49 (3H, s), 3.27 (2H, t, J=7.8 Hz), 1.59 (6H, d, J=6.8 Hz), 1.32 (3H, t, J=7.3 Hz); MS (FAB) m/z 566 (M+).
B-38 mp 174-176° C.; 1H NMR (DMSO-d6) 8.44 (1H, d, J=8.8 Hz), 8.37 (1H, d, J=2.0 Hz), 8.29 (1H, d, J=6.3 Hz), 7.97 (1H, d, J=8.8 Hz), 7.87 (1H, dd, J=7.3, 8.8 Hz), 7.79 (1H, dd, J=2.0, 8.8 Hz), 7.10 (1H, dd, J=6.3, 7.3 Hz), 6.04-5.92 (1H, m), 5.36-5.25 (2H, m), 4.75 (2H, d, J=5.1 Hz), 4.21 (2H, q, J=7.3 Hz), 4.17 (3H, s), 3.98 (3H, s), 1.36 (3H, t, J=7.3 Hz); MS (FAB) m/z 556 (M+).
B-39 mp>300° C. (decomp.); IR (KBr) 1655, 1541, 1489, 1410, 1387, 1153 cm−1; 1H NMR (DMSO-d6) 8.40 (1H, d, J=1.2 Hz), 8.02 (1H, d, J=8.8 Hz), 7.83 (1H, dd, J=1.2, 8.8 Hz), 6.05-5.90 (1H, m), 5.34 (1H, d, J=17.1 Hz), 5.28 (1H, d, J=10.3 Hz), 4.73 (2H, d, J=5.4 Hz), 4.17 (2H, q, J=7.3 Hz), 4.00 (3H, s), 3.96 (2H, t, J=7.6 Hz), 3.48 (3H, s), 3.27 (2H, t, J=7.6 Hz), 1.32 (3H, t, J=7.3 Hz); MS (FAB) m/z 564 (M+).
B-40 mp 296-297° C. (decomp.); IR (KBr) 1636, 1543, 1487, 1435, 1375, 1151 cm−1; 1H NMR (DMSO-d6) 8.44 (1H, d, J=8.9 Hz), 8.23 (1H, d, J=6.5 Hz), 8.02 (1H, d, J=4.4 Hz), 7.78 (1H, dd, J=7.0, 8.9 Hz), 7.74 (1H, d, J=4.4 Hz), 7.03 (1H, dd, J=6.5, 7.0 Hz), 4.25-4.00 (7H, m), 3.86 (3H, s), 1.41-1.20 (6H, m); MS (FAB) m/z 460 (M+).
B-41 mp>250° C. (decomp.); IR (KBr) 1655, 1541, 1416, 1317, 1161 cm−1;
1H NMR (DMSO-d6) 8.05 (1H, d, J=4.4 Hz), 7.82 (1H, d, J=4.4 Hz), 5.99-5.86 (1H, m), 5.33-5.21 (2H, m), 4.65 (2H, d, J=5.6 Hz), 4.13 (2H, q, J=7.3 Hz), 3.94 (2H, t, J=7.8 Hz), 3.87 (3H, s), 3.46 (3H, s), 3.26 (2H, t, J=7.8 Hz), 1.29 (3H, t, J=7.3 Hz); MS (FAB) m/z 480 (M+).
C-2 mp. 224-228° C. (decomp.),
1H-NMR (DMSO-d6), δ 8.40 (br, 1H), 8.01 (d, 1H, J=8.3 Hz), 7.93 (d, 1H, J=7.8 Hz), 7.88 (d, 1H, J=13.2 Hz), 7.82 (m, 1H), 7.53 (t, 1H, J=7.3 Hz), 7.37 (t, 1H, J=8.0 Hz), 6.18 (d, 1H, J=13.2 Hz), 4.09 (q, 2H, J=7.5 Hz), 4.02 (s, 3H), 3.83 (s, 3H), 1.31 (t, 3H, J=7.5 Hz).
C-3 mp. 205-210° C. (decomp.),
1H-NMR (DMSO-d6), δ 8.32 (d, 1H, J=6.1 Hz), 7.86 (d, 1H, J=7.8 Hz), 7.75 (d, 1H, J=7.8 Hz), 7.54-7.49 (m, 2H), 7.41-7.38 (m, 2H), 7.22-7.18 (m, 1H), 5.56 (d, 1H, J=12.5 Hz), 4.02 (s, 3H), 3.93 (q, 2H, J=7.5 Hz), 3.53 (s, 3H), 1.26 (t, 3H, J=7.5 Hz).
C-4 mp. 228-235° C. (decomp.),
1H-NMR (DMSO-d6), δ 7.91-7.89 (m, 2H), 7.84 (d, 1H, J=13.2 Hz), 7.70-7.61 (m, 5H), 7.51 (t, 1H, J=7.5 Hz), 7.34 (t, 1H, J=7.5 Hz), 6.14 (d, 1H, J=13.2 Hz), 4.04 (q, 2H, J=6.8 Hz), 3.79 (s, 3H), 3.72 (s, 3H), 1.28 (t, 3H, J=6.8 Hz).
A-20: mp 282-285° C.; IR (KBr) 1523, 1494, 1303 cm−1; 1H NMR (400 MHz, DMSO-d6) δ 8.59 (d, 1H, J=7.6 Hz), 8.44 (d, 1H, J=6.4 Hz), 8.00 (d, 1H, J=4.8 Hz), 7.72 (d, 1H, J=4.8 Hz), 7.32 (t, 1H, J=8.0 Hz), 4.20 (s, 3H), 4.09 (q, 2H, J=6.8 Hz), 3.07 (s, 3H), 1.31 (t, 3H, J=6.8 Hz); LRMS (FAB+) m/z: 425 (M+).
A-21: orange crystals, mp 275-278° C.; IR (KBr)
1544, 1463, 1429, 1301 cm−1; 1H NMR (400 MHz, DMSO-d6) δ 8.65 (d, 1H, J=7.6 Hz), 8.48 (d, 1H, J=6.4 Hz), 8.26 (d, 1H, J=8.0 Hz), 7.95 (d, 1H, J=8.4 Hz), 7.72 (t, 1H, J=8.0 Hz), 7.56 (t, 1H, J=8.0 Hz), 7.35 (t, 1H, J=7.2 Hz), 4.22 (s, 3H), 4.18-4.15 (m, 2H), 4.01 (s, 3H), 1.35 (t, 3H, J=7.2 Hz); LRMS (FAB+) m/z: 440 (M+).
A-22: orange crystals, mp 275-277° C.; IR (KBr)
1533, 1490, 1305 cm−1; 1H NMR (400 MHz, DMSO-d6) δ 8.73 (d, 1H, J=6.0 Hz), 8.42 (d, 1H, J=7.2 Hz), 8.34 (t, 1H, J=8.0 Hz), 8.27 (d, 1H, J=6.4 Hz), 7.88 (d, 1H, J=8.4 Hz), 7.47 (t, 1H, J=6.8 Hz), 7.16 (t, 1H, J=6.8 Hz), 4.07 (s, 3H), 4.03 (s, 3H), 4.03-3.98 (m, 2H), 1.28 (t, 3H, J=6.8 Hz); LRMS (FAB+) m/z: 384 (M+).
B-42: mp>300° C.; IR (KBr) 1487, 1439 cm−1; 1H NMR (400 MHz, DMSO-d6) δ 8.76 (d, 1H, J=6.8 Hz), 8.40-8.36 (m, 2H), 8.25 (d, 1H, J=6.8 Hz), 7.89 (d, 1H, J=6.0 Hz), 7.53 (t, 1H, J=7.2 Hz), 7.14 (t, 1H, J=7.2 Hz), 4.13 (s, 3H), 4.04-4.00 (m, 7H), 1.30-1.23 (m, 6H); LRMS (FAB+) m/z: 511 (M+).
C-1: green crystals, mp 172-174° C.; IR (KBr): 1521,
1193, 1130 cm−1; 1H NMR (300 MHz, DMSO-d6) δ 8.79 (d, 1H, J=6.3 Hz), 8.40 (t, 1H, J=7.6 Hz), 7.89 (d, 1H, J=8.2 Hz), 7.78 (d, 1H, J=7.6 Hz), 7.62-7.56 (m, 2H), 7.46-7.38 (m, 4H), 7.22 (t, 1H, J=6.6 Hz), 7.10 (d, 1H, J=8.0 Hz), 5.68 (d, 1H, J=12.9 Hz), 4.04 (s, 3H), 3.93 (q, 1H, J=7.7 Hz), 3.58 (s, 3H), 2.26 (s, 3H), 1.24 (t, 3H, J=7.7 Hz).
C-7: green crystals, mp 195-199° C.; IR
(KBr) 1515, 1488, 1149, 1130 cm−1; 1H NMR (400 MHz, DMSO-d6) δ 8.33 (d, 1H, J=13.6 Hz), 8.01-7.81 (m, 4H), 7.76-7.66 (m, 4H), 7.61-7.41 (m, 3H), 5.86 (d, 1H, J=13.6 Hz), 4.10-4.04 (m, 2H), 3.91 (s, 3H), 3.72 (s, 3H), 1.29 (t, 3H, J=6.8 Hz); LRMS (FAB+) m/z: 520 (M+).
C-8: green crystals, mp 239-241° C.; IR (KBr)
1525, 1355, 1274 cm−1; 1H NMR (400 MHz, DMSO-d6) δ 8.27 (d, 1H, J=13.6 Hz), 8.05 (d, 1H, J=4.4 Hz), 7.98-7.77 (m, 5H), 7.70-7.66 (br, 1H), 7.40 (q, 1H, J=7.2 Hz), 5.77 (d, 1H, J=13.6 Hz), 4.04-4.01 (br, 2H), 3.88-3.87 (br, 6H), 1.27 (t, 3H, J=7.2 Hz); LRMS (FAB+) m/z: 409 (M+).
C-9: green crystals, mp 251-253° C.; IR (KBr)
1515, 1355, 1261, 1224 cm−1; 1H NMR (400 MHz, DMSO-d6) δ 8.31 (d, 1H, J=13.6 Hz), 8.24 (d, 1H, J=8.4 Hz), 7.99-7.94 (m, 3H), 7.87 (d, 1H, J=8.4 Hz), 7.82 (d, 1H, J=7.6 Hz), 7.73-7.69 (br, 2H), 7.59-7.41 (m, 2H), 5.87 (d, 1H, J=13.6 Hz), 4.13-4.08 (br, 2H), 4.03 (s, 3H), 3.92 (s, 3H), 1.32 (t, 3H, J=6.8 Hz); LRMS (FAB+) m/z: 459 (M+).
C-10: purple crystals, mp 253-256° C.; IR (KBr)
1508, 1361, 1317, 1191 cm1; 1H NMR (400 MHz, DMSO-d6) δ 8.46 (br, 1H), 7.88-7.78 (m, 3H), 7.59 (d, 1H, J=8.8 Hz), 7.49 (t, 1H, J=7.6 Hz), 7.31 (t, 1H, J=7.6 Hz), 6.08 (d, 1H, J=12.4 Hz), 4.04-4.00 (br, 2H), 3.89 (s, 3H), 3.77 (s, 3H), 1.28-1.25 (br, 3H); LRMS (FAB+) m/z: 415 (M+).
C-11: green crystals, mp 245-247° C.; IR (KBr)
1496, 1458, 1359 cm−1; 1H NMR (400 MHz, DMSO-d6) δ 8.27 (d, 1H, J=8.0 Hz), 8.03-7.87 (m, 3H), 7.78 (t, 1H, J=8.0 Hz), 7.66-7.61 (m, 2H), 7.53 (t, 1H, J=8.0 Hz), 7.37 (t, 1H, J=7.6 Hz), 6.17 (d, 1H, J=13.2 Hz), 4.11 (q, 1H, J=7.2 Hz), 4.05 (s, 3H), 3.82 (s, 3H), 1.32 (t, 3H, J=7.2 Hz); LRMS (FAB+) m/z: 465 (M+).
C-12: green crystals, mp 236-239° C.; IR (KBr)
1506, 1357, 1259, 1149, 1132 cm1; 1H NMR (400 MHz, DMSO-d6) δ 9.14 (s, 1H), 8.51 (d, 1H, J=9.2 Hz), 8.15 (d, 1H, J=13.2 Hz), 7.91 (d, 1H, J=9.2 Hz), 7.84 (d, 1H, J=9.2 Hz), 7.70-7.68 (m, 3H), 7.61 (t, 1H, J=7.6 Hz), 7.30 (t, 1H, J=7.2 Hz), 5.42 (d, 1H, J=12.8 Hz), 4.02 (s, 3H), 3.95 (q, 2H, J=7.2 Hz), 3.68 (s, 3H), 1.25 (t, 3H, J=7.2 Hz); LRMS (FAB+) m/z: 437 (M+).
D-1: purple crystals, mp 298-300° C.; IR
(KBr): 1552, 1494, 1369, 1261, 1136 cm−1; 1H NMR (400 MHz, DMSO-d6) δ 8.78 (d, 1H, J=8.0 Hz), 8.40 (t, 1H, J=7.6 Hz), 8.02-7.97 (m, 1H), 7.90 (d, 1H, J=8.4 Hz), 7.74-7.51 (m, 6H), 7.28 (t, 1H, J=7.2 Hz), 5.47 (d, 1H, J=13.2 Hz), 4.05 (s, 3H), 4.02-3.98 (m, 2H), 3.72 (s, 3H), 3.62-3.58 (m, 2H), 1.29 (t, 3H, J=7.2 Hz), 1.22 (t, 3H, J=7.2 Hz); LRMS (FAB+) m/z: 530 (M+).
D-2: green crystals, mp>300° C.; IR (KBr):
1496, 1369, 1149 cm−1; 1H NMR (400 MHz, DMSO-d6) δ 8.78 (d, 1H, J=5.0 Hz), 8.41 (t, 1H, J=7.2 Hz), 7.88 (d, 1H, J=8.4 Hz), 7.77 (d, 1H, J=7.9 Hz), 7.58 (t, 1H, J=6.5 Hz), 7.48-7.42 (m, 3H), 7.22 (t, 1H, J=6.8 Hz), 5.75 (d, 1H, J=13.2 Hz), 4.05 (s, 3H), 4.02-3.97 (m, 2H), 3.66 (s, 3H), 1.28 (t, 3H, J=6.8 Hz), 1.22 (t, 3H, J=7.6 Hz); LRMS (FAB+) m/z: 536 (M+).
Improved therapeutic/prophylactic agent can be provided by having the compound of the invention as an active ingredient.
This application claims a priority based on the Japanese Patent Application No. 2005-184183 filed on 24 Jun. 2005, and its disclosure including specification and claims is incorporated herein by reference in its entirety.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2005-184183 | Jun 2005 | JP | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/JP2006/311198 | 6/5/2006 | WO | 00 | 3/10/2008 |
