Acid amide derivatives, process for producing these, and pest agent containing these

TECHNICAL FIELD

[0001] The present invention relates to novel acid amide derivatives useful as active ingredients for pesticides.

BACKGROUND ART

[0002] WO 2001/60783 discloses phenacylamine derivatives, a process for their production and pesticides containing them, but there is no specific disclosure relating to acid amide derivatives of the formula (I) given hereinafter.

DISCLOSURE OF THE INVENTION

[0003] Over the years, a number of pesticides have been used, but many of them have various problems such that the effects are inadequate, their use is restricted as the pests have acquired resistance, they have high toxicity against human, animal, fish, etc., and their residual effects disturb the ecological system. Accordingly, it is desired to develop novel pesticides having high safety without such drawbacks.

[0004] Further, parasites on animals are parasitic on the body surfaces, stomachs, intestinal tracts, lungs, hearts, livers, blood vessels, subcutis and lymphatic tissues of domestic animals or companion animals and thus cause various animal diseases, such as anemia, malnutrition, asthenia, weight loss or disorders of intestinal tract walls, organs or other tissues. Accordingly, it is desired to control such parasites.

[0005] The present inventors have conducted various studies on acid amide derivatives to find a superior pesticide. As a result, it has been found that novel acid amide derivatives and their salts have very high controlling effects against pests at low doses, and they show no substantial adverse effects against mammals, fish, etc. The present invention has been accomplished on the basis of this discovery. That is the present invention provides an acid amide derivative of the formula (I) or a salt thereof:

[0006] wherein A is phenyl which may be substituted by X, benzyl which may be substituted by X, naphthyl which may be substituted by X, a heterocyclic group which may be substituted by X, a fused heterocyclic group which may be substituted by X, indanyl (the indanyl may be substituted by halogen, alkyl or alkoxy) or tetrahydronaphthyl (the tetrahydronaphthyl may be substituted by halogen, alkyl or alkoxy), B is alkyl, cycloalkyl, phenyl which may be substituted by Y, a heterocyclic group which may be substituted by Y, or a fused heterocyclic group which may be substituted by Y, X is halogen, alkyl, haloalkyl, alkenyl, haloalkenyl, alkynyl, haloalkynyl, alkoxy, haloalkoxy, alkoxyalkoxy, haloalkoxyalkoxy, alkoxyhaloalkoxy, haloalkoxyhaloalkoxy, alkenyloxy, haloalkenyloxy, alkynyloxy, haloalkynyloxy, alkylthio, haloalkylthio, alkenylthio, haloalkenylthio, alkynylthio, haloalkynylthio, alkylsulfinyl, haloalkylsulfinyl, alkylsulfonyl, haloalkylsulfonyl, dialkylaminosulfonyl, nitro, cyano, phenyl which may be substituted by Y, phenoxy which may be substituted by Y, benzyloxy which may be substituted by Y, pyridyloxy which may be substituted by Y, —OR4, —SR5, —NR6R7, —CO2R8, —C(═O)NR9R10 or an unsaturated heterocyclic group (the unsaturated heterocyclic ring may be substituted by halogen, alkyl, haloalkyl, alkoxy or haloalkoxy), Y is halogen, alkyl, haloalkyl, alkoxy, haloalkoxy, alkylthio, haloalkylthio, alkylsulfinyl, haloalkylsulfinyl, alkylsulfonyl, haloalkylsulfonyl, dialkylaminosulfonyl, nitro, cyano, —OR4, —CO2R11, —CONR12R13 or an unsaturated heterocyclic group (the unsaturated heterocyclic ring may be substituted by halogen, alkyl, haloalkyl, alkoxy or haloalkoxy), each of R1 and R2 is alkyl, cyano or —CO2R14, or R1 and R2 may together form a 3- to 6-membered saturated carbocyclic ring, R3 is hydrogen, alkyl, alkoxyalkyl, alkylthioalkyl, —COR15, —S(O)mR16 or —S(O)nNR17R18, each of R4 and R6 is hydrogen, —C(═W)R19, —C(═W)OR20, —C(═W)SR21, —C(═W)NR22R23, —S(O)qR24 or —S(O)rNR25R26, R5 is hydrogen, —C(═W)R19, —C(═W)OR20, —C(═W)SR21 or —C(═W)NR22R23, R7 is hydrogen, alkyl or haloalkyl, each of R8, R9, R10, R11, R12, R13 and R14 is hydrogen or alkyl, R15 is hydrogen, alkyl or alkoxy, each of R16, R17, R18, R19, R20, R21, R22, R23, R24, R25 and R26 is alkyl, haloalkyl or phenyl (the phenyl which may be substituted by halogen, alkyl, haloalkyl, alkoxy or haloalkoxy), each of m, n, q and r is from 0 to 2, W is oxygen or sulfur, provided that (1) a case where A is phenyl which may be substituted by X1, B is alkyl, cycloalkyl, phenyl which may be substituted by Y1, pyridyl which may be substituted by Y1 or pyrazolyl which may be substituted by Y1, each of R1 and R2 is alkyl, or R1 and R2 together form a 3- to 6-membered saturated carbocyclic ring, R3 is hydrogen, alkyl, alkoxyalkyl, alkylthioalkyl, alkylcarbonyl or alkoxycarbonyl, X1 is halogen, alkyl, haloalkyl, alkenyl, haloalkenyl, alkynyl, haloalkynyl, alkoxy, haloalkoxy, alkenyloxy, haloalkenyloxy, alkynyloxy, haloalkynyloxy, alkylthio, haloalkylthio, alkenylthio, haloalkenylthio, alkynylthio, haloalkynylthio, alkylsulfinyl, haloalkylsulfinyl, alkylsulfonyl, haloalkylsulfonyl, dialkylaminosulfonyl, nitro, cyano, phenyl which may be substituted by Y1, phenoxy which may be substituted by Y1, benzyloxy which may be substituted by Y1 or pyridyloxy which may be substituted by Y1, and Y1 is halogen, alkyl, haloalkyl, alkoxy, haloalkoxy, alkylthio, haloalkylthio, alkylsulfinyl, haloalkylsulfinyl, alkylsulfonyl, haloalkylsulfonyl, dialkylaminosulfonyl, nitro or cyano, and (2) N-[1-methyl-1-(2′-methylisonicotinoyl)ethyl]benzamide, are excluded; a process for its production; and a pesticide containing it.

[0007] The number of substituents X in the phenyl which may be substituted by X, the benzyl which may be substituted by X, the naphthyl which may be substituted by X, the heterocyclic group which may be substituted by X or the fused heterocyclic group which may be substituted by X, in A, may be one or more, and in the case of more than one, such substituents may be the same or different, and the number of substituents Y in the phenyl which may be substituted by Y, the heterocyclic group which may be substituted by Y or the fused heterocyclic group which may be substituted by Y, in B, or the number of substituents Y in the phenyl which may be substituted by Y, the phenoxy which may be substituted by Y, the benzyloxy which may be substituted by Y or the pyridyloxy which may be substituted by Y, in X, may be one or more, and in the case of more than one, such substituents may be the same or different. The number of halogen, alkyl or alkoxy which is substituent of indanyl or tetrahydronaphthyl, may be one or more, and in the case of more than one, such substituents may be the same or different. The number of the substituent of the unsaturated heterocyclic group in X or Y, or the number of the substituent of the phenyl in R16 to R26, may be one or more, and in the case of more than one, such substituents may be the same or different.

[0008] The heterocyclic group in A or B, is a 5- or 6-membered heterocyclic group containing from 1 to 4 atoms of at least one type selected from the group consisting of O, S and N, such as furyl, tetrahydrofuryl, thienyl, pyrrolyl, pyrrolinyl, pyrrolidinyl, dioxolanyl, oxazolyl, isoxazolyl, thiazolyl, isothiazolyl, imidazolyl, imidazolinyl, imidazolidinyl, pyrazolyl, pyrazolinyl, pyrazolidinyl, triazolyl, oxadiazolyl, thiadiazolyl, tetrazolyl, pyranyl, pyridyl, piperidinyl, dioxanyl, oxazinyl, morpholinyl, thiazinyl, pyridazinyl, pyrimidinyl, pyrazinyl, piperazinyl or triazinyl.

[0009] The fused heterocyclic group in A or B, is a 8- to 10-membered fused heterocyclic group containing from 1 to 4 atoms of at least one type selected from the group consisting of O, S and N, such as benzofuranyl, isobenzofuranyl, dihydrobenzofuranyl, dihydroisobenzofuranyl, benzothienyl, isobenzothienyl, dihydrobenzothienyl, dihydroisobenzothienyl, tetrahydrobenzothienyl, indolyl, isoindolyl, benzoxazolyl, benzothiazolyl, indazolyl, benzimidazolyl, benzodioxolanyl, benzodioxanyl, chromenyl, chromanyl, isochromanyl, chromonyl, chromanonyl, quinolyl, isoquinolyl, cinnolinyl, phthalazinyl, quinazolinyl, quinoxalinyl, indolizinyl, quinolizinyl, imidazopyridyl, naphthyridinyl, pteridinyl, dihydrobenzoxazinyl, dihydrobenzoxazolinonyl, dihydrobenzoxazinonyl or benzothioxanyl.

[0010] The unsaturated heterocyclic group in X or Y, is a 5- to 6-membered unsaturated heterocyclic group containing from 1 to 4 atoms of at. least one type selected from the group consisting of O, S and N, such as furyl, thienyl, pyrrolyl, pyrrolinyl, oxazolyl, isoxazolyl, thiazolyl, isothiazolyl, imidazolyl, imidazolinyl, pyrazolyl, pyrazolinyl, triazolyl, oxadiazolyl, thiadiazolyl, tetrazolyl, pyranyl, pyridyl, oxazinyl, thiazinyl, pyridazinyl, pyrimidinyl, pyrazinyl, or triazinyl.

[0011] The alkyl or alkyl moiety in B, X, Y, R1 to R3 or R7 to R26, the alkyl or alkyl moiety as a substituent of indanyl or tetrahydronaphthyl, in A, the alkyl or alkyl moiety as a substituent of unsaturated heterocyclic group in X or Y, or, the alkyl or alkyl moiety as a substituent of phenyl in R16 to R26, may be linear or branched one having from 1 to 6 carbon atoms, such as methyl, ethyl, propyl, isopropyl, butyl, tert-butyl, pentyl or hexyl.

[0012] The cycloalkyl in B may be one having from 3 to 6 carbon atoms, such as cyclopropyl, cyclopentyl or cyclohexyl.

[0013] The alkenyl or alkenyl moiety in X may be linear or branched one having from 2 to 7 carbon atoms, such as vinyl, 1-propenyl, allyl, isopropenyl, 1-butenyl, 1,3-butadienyl, 1-hexenyl or 1-heptenyl. Further, the alkynyl or alkynyl moiety in X may be linear or branched one having from 2 to 7 carbon atoms, such as ethynyl, 2-butynyl, 2-pentynyl, 3-hexynyl or 4-dimethyl-2-pentynyl.

[0014] As the halogen or the halogen as a substituent in A, X, Y, R7 or R16 to R26 (include halogen as a substituent of indanyl or tetrahydronaphthyl, in A, halogen as a substituent of unsaturated heterocyclic group in X and Y, and halogen as a substituent of phenyl in R16 to R26), an atom of fluorine, chlorine, bromine or iodine may be mentioned. The number of halogens as substituents may be one or more, and in a case where it is more than one, the respective halogens may be the same or different. Further, such halogens may be substituted at any position.

[0015] The salt of the acid amide derivative of the above formula (I) may be any salt so long as it is agriculturally acceptable. For example, it may be an alkali metal salt such as a sodium salt or a potassium salt; an alkaline earth metal salt such as a magnesium salt or a calcium salt; an ammonium salt such as a dimethylamine salt or a triethylamine salt; an inorganic salt such as a hydrochloride, a perchlorate, a sulfate or a nitrate; or an organic salt such as an acetate or a methanesulfonate.

[0016] The acid amide derivative of the above formula (I) has various isomers such as optical isomers and tautomeric isomers, and the present invention includes both isomers and mixtures of such isomers. Further, the present invention also includes various isomers other than the above isomers within the common knowledge in the technical field concerned.

[0017] The acid amide derivative of the above formula (I) or a salt thereof (hereinafter referred to simply as the compound of the present invention) can be produced by the following reactions (A) to (K), or by a usual process for producing a salt.

[0018] (II) or a salt thereof (I-1)

[0019] In the reaction (A), A, B, R1, and R2, are as defined above. Z is hydroxy, alkoxy or halogen, and the halogen may be an atom of fluorine, chlorine, bromine or iodine.

[0020] Reaction (A) is carried out usually in the presence of a base and a solvent.

[0021] The base may be one or more suitably selected from e.g. an alkali metal such as sodium or potassium; an alkali metal alcoholate such as sodium methylate, sodium ethylate or potassium tertiary butoxide; a carbonate such as sodium carbonate or potassium carbonate; a bicarbonate such as sodium bicarbonate or potassium bicarbonate; a metal hydroxide such as sodium hydroxide or potassium hydroxide; a metal hydride such as sodium hydride or potassium hydride; an amine such as monomethylamine, dimethylamine or triethylamine; and a pyridine such as pyridine or 4-dimethylaminopyridine. The base is used in an amount of from 1 to 3 mols, preferably from 1 to 2 mols, per mol of the compound of the formula (II).

[0022] The solvent may be any solvent so long as it is a solvent inert to the reaction. For example, it may be one or more suitably selected from e.g. an aromatic hydrocarbon such as benzene, toluene, xylene or chlorobenzene; an aliphatic hydrocarbon such as carbon tetrachloride, methyl chloride, chloroform, dichloromethane, dichloroethane, trichloroethane, hexane or cyclohexane; an ether such as dioxane, tetrahydrofuran, diethyl ether or dimethoxyethane; an ester such as methyl acetate or ethyl acetate; a polar aprotic solvent such as dimethyl sulfoxide, sulfolane, dimethylacetamide, dimethylformamide, N-methylpyrrolidone or pyridine; a nitrile such as acetonitrile, propionitrile or acrylonitrile and a ketone such as acetone or methyl ethyl ketone.

[0023] Reaction (A) is carried out, if necessary, in the presence of a dehydration condensation agent. The dehydration condensation agent may, for example, be N,N′-dicyclohexylcarbodiimide, chlorosulfonyl isocyanate, N,N′-carbonyldiimidazole and trifluoroacetic anhydride.

[0024] The reaction temperature for reaction (A) is usually from 0 to 100° C., preferably from 0 to 50° C., and the reaction time is usually from 0.5 to 48 hours, preferably from 1 to 24 hours.

[0025] In reaction (B), A, B, R1 and R2 are as defined above, and R3a is alkyl, alkoxyalkyl, alkylthioalkyl, —COR15, —S(O)mR16 or —S(O)nNR17R18 (wherein R15, R16, R17, R18, m and n are as defined above), and T is halogen, and the halogen may be an atom of fluorine, chlorine, bromine or iodine.

[0026] Reaction (B) is carried out usually in the presence of a base and a solvent.

[0027] The base may be one or more suitably selected from e.g. an alkali metal such as sodium or potassium; an alkali metal alcoholate such as sodium methylate, sodium ethylate or potassium tertiary butoxide; a carbonate such as sodium carbonate or potassium carbonate; a bicarbonate such as sodium bicarbonate or potassium bicarbonate; a metal hydroxide such as sodium hydroxide or potassium hydroxide; a metal hydride such as sodium hydride or potassium hydride; an amine such as monomethylamine, dimethylamine or triethylamine; and a pyridine such as pyridine or 4-dimethylaminopyridine. The base is used in an amount of from 1 to 3 mols, preferably from 1 to 1.5 mols, per mol of the compound of the formula (I-1).

[0028] The solvent may be any solvent so long as it is a solvent inert to the reaction. For example, it may be one or more suitably selected from e.g. an aromatic hydrocarbon such as benzene, toluene, xylene or chlorobenzene; an aliphatic hydrocarbon such as carbon tetrachloride, methyl chloride, chloroform, dichloromethane, dichloroethane, trichloroethane, hexane or cyclohexane; an ether such as dioxane, tetrahydrofuran, diethyl ether or dimethoxyethane; an ester such as methyl acetate or ethyl acetate; a polar aprotic solvent such as dimethyl sulfoxide, sulfolane, dimethylacetamide, dimethylformamide, N-methylpyrrolidone or pyridine; a nitrile such as acetonitrile, propionitrile or acrylonitrile; and a ketone such as acetone or methyl ethyl ketone.

[0029] The reaction temperature for reaction (B) is usually from 0 to 100° C., preferably from 0 to 50° C., and the reaction time is usually from 1 to 300 hours, preferably from 1 to 150 hours.

[0030] (II) or a salt thereof

[0031] In reaction (C), A, R1 and R2 are as defined above, and B1 is phenyl substituted by —CO2H, a heterocyclic group substituted by —CO2H, or a fused heterocyclic group substituted by —CO2H. The formula (V) is anhydrous dicarboxylic acid of Q (phenyl, a heterocyclic group or a fused heterocyclic group).

[0032] Reaction (C) is carried out usually in the presence of a solvent. The solvent may be any solvent so long as it is a solvent inert to the reaction. For example, it may be one or more suitably selected from e.g. an aromatic hydrocarbon such as benzene, toluene, xylene or chlorobenzene; an aliphatic hydrocarbon such as carbon tetrachloride, methyl chloride, chloroform, dichloromethane, dichloroethane, trichloroethane, hexane or cyclohexane; an ether such as dioxane, tetrahydrofuran, diethyl ether or dimethoxy ethane; an ester such as methyl acetate or ethyl acetate; a polar aprotic solvent such as dimethyl sulfoxide, sulfolane, dimethylacetamide, dimethylformamide, N-methylpyrrolidone or pyridine; a nitrile such as acetonitrile, propionitrile or acrylonitrile; a ketone such as acetone or methyl ethyl ketone; and an alcohol such as methanol, ethanol, propanol or tert-butanol.

[0033] Reaction (C) is carried out, if necessary, in the presence of a base. The base may be one or more suitably selected from e.g. an alkali metal such as sodium or potassium; an alkali metal alcoholate such as sodium methylate, sodium ethylate or potassium tertiary butoxide; a carbonate such as sodium carbonate or potassium carbonate; a bicarbonate such as sodium bicarbonate or potassium bicarbonate; a metal hydroxide such as sodium hydroxide or potassium hydroxide; a metal hydride such as sodium hydride or potassium hydride; an amine such as monomethylamine, dimethylamine or triethylamine; and a pyridine such as pyridine or 4-dimethylaminopyridine. The base is used in an amount of from 1 to 3 mols, preferably from 1 to 1.5 mols, per mol of the compound of the formula (II).

[0034] The reaction temperature for reaction (C) is usually from 0 to 150° C., preferably from 0 to 80° C. The reaction time is usually from 0.5 to 96 hours, preferably from 1 to 48 hours.

[0035] In reaction (D), A, R1 and R2 are as defined above. B2 is phenyl substituted by Y2, a heterocyclic group substituted by Y2, or a fused heterocyclic group substituted by Y2, B3 is phenyl substituted by Y3, a heterocyclic group substituted by Y3, or a fused heterocyclic group substituted by Y3, Y2 is an atom of chlorine, bromine or iodine, and Y3 is an unsaturated heterocyclic group (the unsaturated heterocyclic ring may be substituted by halogen, alkyl, haloalkyl, alkoxy or haloalkoxy).

[0036] Reaction (D) is carried out usually in the presence of a catalyst, a base, a solvent and an inert gas.

[0037] The catalyst may be one or more suitably selected from e.g. palladium complexes such as tetrakis (triphenylphosphine)palladium(0), bis (dibenzylideneacetone)palladium(0), and tris (dibenzylideneacetone)dipalladium(0).

[0038] The base may be one or more suitably selected from e.g. a carbonate such as sodium carbonate, potassium carbonate or calcium carbonate; a bicarbonate such as sodium bicarbonate or potassium bicarbonate; and a metal hydroxide such as sodium hydroxide or potassium hydroxide. The base is used in an amount of from 1 to 20 mols, preferably from 1 to 10 mols, per mol of the compound of the formula (I-4).

[0039] The solvent may be any solvent so long as it is a solvent inert to the reaction. For example, it may be one or more suitably selected from e.g. an aromatic hydrocarbon such as benzene, toluene, xylene or chlorobenzene; an aliphatic hydrocarbon such as carbon tetrachloride, methyl chloride, chloroform, dichloromethane, dichloroethane, trichloroethane, hexane or cyclohexane; an ether such as dioxane, tetrahydrofuran, diethyl ether or dimethoxyethane; an ester such as methyl acetate or ethyl acetate; a polar aprotic solvent such as dimethyl sulfoxide, sulfolane, dimethylacetamide, dimethylformamide, N-methylpyrrolidone or pyridine; a nitrile such as acetonitrile, propionitrile or acrylonitrile; a ketone such as acetone or methyl ethyl ketone; an alcohol such as methanol, ethanol, propanol or tert-butanol; and water.

[0040] The inert gas may, for example, be nitrogen gas or argon gas.

[0041] The reaction temperature for reaction (D) is usually from 0 to 150° C., preferably from 15 to 100° C. The reaction time is usually from 0.5 to 96 hours, preferably from 1 to 48 hours.

[0042] In reaction (E), A, R1 and R2 are as defined above, and B4 is phenyl substituted by —CO2H, a heterocyclic group substituted by —CO2H, or a fused heterocyclic group substituted by —CO2H, B5 is phenyl substituted by —CO2 R11a, a heterocyclic group substituted by —CO2 R11a, or a fused heterocyclic group substituted by —CO2 R11a, and R11a is alkyl.

[0043] The first step in reaction (E) is carried out in the presence of a chlorination agent. The chlorination agent may be one or more suitably selected from e.g. thionyl chloride, oxalyl chloride and phosphorus pentachloride.

[0044] The first step in reaction (E) is carried out, if necessary, in the presence of a solvent. The solvent may be any solvent so long as it is a solvent inert to the reaction. For example, it may be one or more suitably selected from e.g. an aromatic hydrocarbon such as benzene, toluene, xylene or chlorobenzene; an aliphatic hydrocarbon such as carbon tetrachloride, methyl chloride, chloroform, dichloromethane, dichloroethane, trichloroethane, hexane or cyclohexane; an ether such as dioxane, tetrahydrofuran, diethyl ether or dimethoxyethane; and an ester such as methyl acetate or ethyl acetate.

[0045] The reaction temperature for the first step in reaction (E) is usually from 0 to 200° C., preferably from 15 to 150° C. The reaction time is usually from 0.1 to 72 hours, preferably from 0.5 to 3 hours.

[0046] The second step in reaction (E) is carried out, if necessary, in the presence of a base. The base may be one or more suitably selected from e.g. an alkali metal such as sodium or potassium; an alkali metal alcoholate such as sodium methylate, sodium ethylate or potassium tertiary butoxide; a carbonate such as sodium carbonate or potassium carbonate; a bicarbonate such as sodium bicarbonate or potassium bicarbonate; a metal hydroxide such as sodium hydroxide or potassium hydroxide; a metal hydride such as sodium hydride or potassium hydride; an amine such as monomethylamine, dimethylamine or triethylamine; and a pyridine such as pyridine or 4-dimethylaminopyridine. The base is used in an amount of from 1 to 5 mols, preferably from 1 to 2 mols, per mol of the compound of the formula (I-6).

[0047] The second step in reaction (E) is carried out, if necessary, in the presence of a solvent. The solvent may be any solvent so long as it is a solvent inert to the reaction. For example, it may be one or more suitably selected from e.g. an aromatic hydrocarbon such as benzene, toluene, xylene or chlorobenzene; an aliphatic hydrocarbon such as carbon tetrachloride, methyl chloride, chloroform, dichloromethane, dichloroethane, trichloroethane, hexane or cyclohexane; an ether such as dioxane, tetrahydrofuran, diethyl ether or dimethoxyethane; an ester such as methyl acetate or ethyl acetate; a polar aprotic solvent such as dimethyl sulfoxide, sulfolane, dimethylacetamide, dimethylformamide, N-methylpyrrolidone or pyridine; a nitrile such as acetonitrile, propionitrile or acrylonitrile; and a ketone such as acetone or methyl ethyl ketone. Further, in this reaction, the compound of the formula (VII) may serve also as a solvent if used excessively.

[0048] The reaction temperature for the second step in reaction (E) is usually from 0 to 100° C., preferably from 0 to 50° C. The reaction time is usually from 0.1 to 48 hours, preferably from 0.5 to 6 hours.

[0049] In reaction (F), A, B4 B5, R1, R2 and B11a are as defined above.

[0050] Reaction (F) is carried out usually in the presence of a catalyst or a dehydration condensation agent.

[0051] The catalyst may be one or more suitably selected from e.g. a mineral acid such as hydrochloric acid or sulfuric acid; an organic acid such as paratoluene sulfonic acid; and a Lewis acid such as boron trifluoride etherate.

[0052] The dehydration condensation agent may be one or more suitably selected from e.g. N,N′-dicyclohexylcarbodiimide, chlorosulfonyl isocyanate, N,N′-carbonyldiimidazole and trifluoroacetic anhydride.

[0053] Reaction (F) is carried out, if necessary, in the presence of a solvent. The solvent may be any solvent so long as it is a solvent inert to the reaction. For example, it may be one or more suitably selected from e.g. an aromatic hydrocarbon such as benzene, toluene, xylene or chlorobenzene; an aliphatic hydrocarbon such as carbon tetrachloride, methyl chloride, chloroform, dichloromethane, dichloroethane, trichloroethane, hexane or cyclohexane; an ether such as dioxane, tetrahydrofuran, diethyl ether or dimethoxyethane; an ester such as methyl acetate or ethyl acetate; a polar aprotic solvent such as dimethyl sulfoxide, sulfolane, dimethylacetamide, dimethylformamide, N-methylpyrrolidone or pyridine; a nitrile such as acetonitrile, propionitrile or acrylonitrile; a ketone such as acetone or methyl ethyl ketone; and an alcohol such as methanol, ethanol, propanol or tert-butanol. Further, in this reaction, the compound of the formula (VII) may serve also as a solvent if used excessively.

[0054] The reaction temperature for reaction (F) is usually from 0 to 200° C., preferably from 0 to 100° C. The reaction time is usually from 0.1 to 96 hours, preferably from 0.5 to 24 hours.

[0055] In reaction (G), A, B4, R1, R2, R12 and R13 are as defined above, and B6 is phenyl substituted by —CONR12R13, a heterocyclic group substituted by —CONR12R13, or a fused heterocyclic group substituted by —CONR12R13 (wherein R12 and R13 are as defined above)

[0056] The first step in reaction (G) is carried out in accordance with the first step in the above-described reaction (E).

[0057] The second step in the reaction (G) is carried out, if necessary, in the presence of a base. The base may be one or more suitably selected from e.g. an alkali metal such as sodium or potassium; an alkali metal alcoholate such as sodium methylate, sodium ethylate or potassium tertiary butoxide; a carbonate such as sodium carbonate or potassium carbonate; a bicarbonate such as sodium bicarbonate or potassium bicarbonate; a metal hydroxide such as sodium hydroxide or potassium hydroxide; a metal hydride such as sodium hydride or potassium hydride; an amine such as monomethylamine, dimethylamine or triethylamine; and a pyridine such as pyridine or 4-dimethylaminopyridine. The base is used in an amount of from 1 to 10 mols, preferably from 1 to 2 mols, per mol of the compound of the formula (I-6).

[0058] The second step in reaction (G) is carried out, if necessary, in the presence of a solvent. The solvent may be any solvent so long as it is a solvent inert to the reaction. For example, it may be one or more suitably selected from e.g. an aromatic hydrocarbon such as benzene, toluene, xylene or chlorobenzene; an aliphatic hydrocarbon such as carbon tetrachloride, methyl chloride, chloroform, dichloromethane, dichloroethane, trichloroethane, hexane or cyclohexane; an ether such as dioxane, tetrahydrofuran, diethyl ether or dimethoxyethane; an ester such as methyl acetate or ethyl acetate; a polar aprotic solvent such as dimethyl sulfoxide, sulfolane, dimethylacetamide, dimethylformamide, N-methylpyrrolidone or pyridine; a nitrile such as acetonitrile, propionitrile or acrylonitrile; a ketone such as acetone or methyl ethyl ketone; and water.

[0059] The reaction temperature for the second step in reaction (G) is usually from 0 to 100° C., preferably from 0 to 50° C. The reaction time is usually from 0.1 to 48 hours, preferably from 0.5 to 6 hours.

[0060] In reaction (H), A, B4, B6, R1, R2, R12 and B13 are as defined above.

[0061] Reaction (H) is carried out usually in the presence of a dehydration condensation agent and a solvent.

[0062] The dehydration condensation agent may be one or more suitably selected from e.g. N,N′-dicyclohexylcarbodiimide, chlorosulfonyl isocyanate, N,N′-carbonyldiimidazole and trifluoroacetic anhydride.

[0063] The solvent may be any solvent so long as it is a solvent inert to the reaction. For example, it may be one or more suitably selected from e.g. an aromatic hydrocarbon such as benzene, toluene, xylene or chlorobenzene; an aliphatic hydrocarbon such as carbon tetrachloride, methyl chloride, chloroform, dichloromethane, dichloroethane, trichloroethane, hexane or cyclohexane; an ether such as dioxane, tetrahydrofuran, diethyl ether or dimethoxyethane; an ester such as methyl acetate or ethyl acetate; a polar aprotic solvent such as dimethyl sulfoxide, sulfolane, dimethylacetamide, dimethylformamide, N-methylpyrrolidone or pyridine; a nitrile such as acetonitrile, propionitrile or acrylonitrile; and a ketone such as acetone or methyl ethyl ketone.

[0064] The reaction temperature for the reaction (H) is usually from 0 to 200° C., preferably from 0 to 100° C. The reaction time is usually from 0.1 to 96 hours, preferably from 0.5 to 24 hours.

[0065] In reaction (I), A, B5, B6, R1, R2, R12 and R13 are as defined above.

[0066] Reaction (I) is carried out usually in the presence of a solvent. The solvent may be any solvent so long as it is a solvent inert to the reaction. For example, it may be one or more suitably selected from e.g. an aromatic hydrocarbon such as benzene, toluene, xylene or chlorobenzene; an aliphatic hydrocarbon such as carbon tetrachloride, methyl chloride, chloroform, dichloromethane, dichloroethane, trichloroethane, hexane or cyclohexane; an ether such as dioxane, tetrahydrofuran, diethyl ether or dimethoxyethane; an ester such as methyl acetate or ethyl acetate; a polar aprotic solvent such as dimethyl sulfoxide, sulfolane, dimethylacetamide, dimethylformamide, N-methylpyrrolidone or pyridine; a nitrile such as acetonitrile, propionitrile or acrylonitrile; a ketone such as acetone or methyl ethyl ketone; an alcohol such as methanol, ethanol, propanol or tert-butanol; and water. Further, in this reaction, the compound of the formula (VIII) may serve also as a solvent if used excessively.

[0067] The reaction temperature for the reaction (I) is usually from 0 to 150° C., preferably from 0 to 80° C. The reaction time is usually from 0.1 to 48 hours, preferably from 0.5 to 24 hours.

[0068] In reaction (J), B is as defined above, A1 is phenyl substituted by —OR4a, benzyl substituted by —OR4a, naphthyl substituted by —OR4a, a heterocyclic group substituted by —OR4a or a fused heterocyclic group substituted by —OR4a, A2 is phenyl substituted by —OH, benzyl substituted by —OH, naphthyl substituted by —OH, a heterocyclic group substituted by —OH or a fused heterocyclic group substituted by —OH, each of R1a and R2a is alkyl or cyano. R1a and R2a may together form a 3- to 6-membered saturated carbocycle, R4a is —C(═W)R19, —C(═W)OR20, —C(═W)SR21, —C(═W)NR22R23, —S(O)qR24 or —S(O)rNR25R26 (wherein R19 to R26, W, q and r are as defined above), and M is sodium or potassium.

[0069] Reaction (J) is usually carried out in the presence of a solvent. The solvent may be any solvent so long as it is a solvent inert to the reaction. For example, it may be one or more suitably selected from e.g. an aromatic hydrocarbon such as benzene, toluene, xylene or chlorobenzene; an aliphatic hydrocarbon such as carbon tetrachloride, methyl chloride, chloroform, dichloromethane, dichloroethane, trichloroethane, hexane or cyclohexane; an ether such as dioxane, tetrahydrofuran, diethyl ether or dimethoxyethane; a polar aprotic solvent such as dimethyl sulfoxide, sulfolane, dimethylacetamide, dimethylformamide, N-methylpyrrolidone or pyridine; a nitrile such as acetonitrile, propionitrile or acrylonitrile; a ketone such as acetone or methyl ethyl ketone;an alcohol such as methanol, ethanol, propanol or tert-butanol; and water.

[0070] The reaction temperature for reaction (J) is usually from 0 to 100° C., preferably from 20 to 80° C. The reaction time is usually from 0.1 to 24 hours, preferably from 0.1 to 12 hours.

[0071] In reaction (K), A1, A2, B, R1a, R2a and R4a are as defined above, G is an atom of chlorine, bromine or iodine.

[0072] Reaction (K) is usually carried out in the presence of a base and a solvent.

[0073] The base may be one or more suitably selected from e.g. an alkali metal alcoholate such as sodium methylate, sodium ethylate or potassium tertiary butoxide; a carbonate such as sodium carbonate or potassium carbonate; a bicarbonate such as sodium bicarbonate or potassium bicarbonate; a metal hydroxide such as sodium hydroxide or potassium hydroxide; a metal hydride such as sodium hydride or potassium hydride; an amine such as monomethylamine, dimethylamine or triethylamine; and a pyridine such as pyridine or 4-dimethylaminopyridine. The base is used in an amount of from 1 to 2 mols, preferably from 1 to 1.5 mols, per mol of the compound of the formula (I-10).

[0074] The solvent may be any solvent so long as it is a solvent inert to the reaction. For example, it may be one or more suitably selected from e.g. an aromatic hydrocarbon such as benzene, toluene, xylene or chlorobenzene; an aliphatic hydrocarbon such as carbon tetrachloride, methyl chloride, chloroform, dichloromethane, dichloroethane, trichloroethane, hexane or cyclohexane; an ether such as dioxane, tetrahydrofuran, diethyl ether or dimethoxyethane; an ester such as methyl acetate or ethyl acetate; a polar aprotic solvent such as dimethyl sulfoxide, sulfolane, dimethylacetamide, dimethylformamide, N-methylpyrrolidone or pyridine; a nitrile such as acetonitrile, propionitrile or acrylonitrile; and a ketone such as acetone or methyl ethyl ketone.

[0075] The reaction temperature for reaction (K) is usually from −20 to 100° C., preferably from 0 to 50° C. The reaction time is usually from 0.1 to 24 hours, preferably from 0.1 to 12 hours.

[0076] The compound of the formula (II) to be used in the above reaction (A) or (C) is novel and can be produced by the following reactions (L) to (N).

[0077] In reaction (L), A, R1 and R2 are as defined above. In reaction (L), a salt of the compound (II) can be produced by post treatment of the reaction or in accordance with a usual reaction for forming a salt.

[0078] Reaction (L) is carried out usually in the presence of an oxidizing agent and a solvent.

[0079] The oxidizing agent may, for example, be potassium ferricyanide. The oxidizing agent is used in an amount of from 1 to 10 mols, preferably from 1 to 5 mols, per mol of the compound of the formula (XII).

[0080] The solvent may be any solvent so long as it is inert to the reaction. For example, it may be one or more suitably selected from e.g. an ether such as dioxane, tetrahydrofuran, diethyl ether or dimethoxyethane; an ester such as methyl acetate or ethyl acetate; a polar aprotic solvent such as dimethyl sulfoxide, sulfolane, dimethylacetamide, dimethylformamide, N-methylpyrrolidone or pyridine; a nitrile such as acetonitrile, propionitrile or acrylonitrile; a ketone such as acetone or methyl ethyl ketone; and water.

[0081] The reaction temperature for reaction (L) is usually from 20 to 150° C., preferably from 50 to 100° C. The reaction time is usually from 0.5 to 30 hours, preferably from 1 to 20 hours.

[0082] In reaction (M), A, R1 and R2 are as defined above. In reaction (M), a salt of the compound (II) can be roduced by post treatment of the reaction or in accordance with a usual reaction for forming a salt.

[0083] The cyclization reaction in reaction (M) is carried out usually in the presence of a base and a solvent.

[0084] The base may be one or more suitably selected from e.g. an alkali metal such as sodium or potassium; an alkali metal alcoholate such as sodium methylate, sodium ethylate or potassium tert-butoxide; and a metal hydride such as sodium hydride or potassium hydride. The base is used in an amount of from 1 to 3 mols, preferably from 1 to 1.5 mols per mol of the compound of the formula (XIII).

[0085] The solvent may be any solvent so long as it is inert to the reaction. For example, it may be one or more suitably selected from e.g. an aromatic hydrocarbon such as benzene, toluene, xylene or chlorobenzene; an ether such as dioxane, tetrahydrofuran, diethyl ether or dimethoxyethane; an alcohol such as methanol, ethanol, propanol or tert-butanol; and a nitrile such as acetonitrile, propionitrile or acrylonitrile.

[0086] The reaction temperature for the cyclization reaction in reaction (M) is usually from 0 to 150° C., preferably from 30 to 100° C. The reaction time is usually from 0.5 to 24 hours, preferably from 1 to 12 hours.

[0087] The hydrolytic reaction in reaction (M) may be carried out in accordance with a common hydrolytic reaction and is carried out usually in the presence of an acid or base and a solvent.

[0088] The acid may, for example, be hydrogen chloride or sulfuric acid. The base may, for example, be a metal hydroxide such as sodium hydroxide or potassium hydroxide.

[0089] The solvent may be any solvent so long as it is inert to the reaction. For example, it may be one or more suitably selected e.g. an alcohol such as methanol, ethanol, propanol or tert-butanol; a nitrile such as acetonitrile, propionitrile or acrylonitrile; a ketone such as acetone or methyl ethyl ketone; and water.

[0090] The reaction temperature for the hydrolytic reaction in reaction (M) is usually from 0 to 100° C., preferably from 20 to 80° C. The reaction time is usually from 0.1 to 12 hours, preferably from 0.1 to 1 hour.

[0091] In reaction (N), A, R1 and R2 are as defined above. In reaction (N), a salt of the compound (II) can be produced by post treatment of the reaction or in accordance with a usual reaction for forming a salt.

[0092] The reduction reaction in reaction (N) may, for example, be catalytic reduction, reduction by a metal hydride (such as sodium boron hydride, or lithium aluminum hydride) or reduction by e.g. triphenylphosphine or sulfide. The catalytic reduction is usually carried out by reacting with hydrogen, formic acid, ammonium formate, an alcohol, cyclohexane, triethylammonium formate or ammonium chloride, in the presence of a catalyst. The catalyst may be one or more suitably selected from e.g. platinum, platinum oxide, platinum black, Raney Nickel, palladium, palladium-carbon, rhodium, rhodium-alumina, iron and copper.

[0093] Reaction (N) is carried out usually in the presence of a solvent. The solvent may be any solvent so long as it is a solvent inert to the reaction. For example, it may be one or more suitably selected from e.g. an aromatic hydrocarbon such as benzene, toluene or xylene; an aliphatic hydrocarbon such as hexane or cyclohexane; an ether such as dioxane, tetrahydrofuran, diethyl ether or dimethoxyethane; an ester such as methyl acetate or ethyl acetate; a polar aprotic solvent such as dimethyl sulfoxide, sulfolane, dimethylacetamide, dimethylformamide, N-methylpyrrolidone or pyridine; a nitrile such as acetonitrile, propionitrile or acrylonitrile; a ketone such as acetone or methyl ethyl ketone; an alcohol such as methanol, ethanol, propanol or tert-butanol; and water.

[0094] The reaction temperature in reaction (N) is usually from 0 to 150° C., preferably from 0 to 80° C. The reaction time is usually from 0.5 to 96 hours, preferably from 1 to 48 hours.

[0095] The compound of the formula (XIII) to be used in the above reaction (M) is novel and can be produced by the following reaction (O).

[0096] In reaction (O), A, R1 and R2 are as defined above.

[0097] Reaction (O) may be carried out, if necessary, in the presence of a solvent. The solvent may be any solvent so long as it is inert to the reaction, and for example, it may be one or more suitably selected from e.g. an aromatic hydrocarbon such as benzene, toluene, xylene or chlorobenzene; an aliphatic hydrocarbon such as carbon tetrachloride, chloroform, dichloromethane, dichloroethane, trichloroethane, hexane or cyclohexane; an ether such as dioxane, tetrahydrofuran, diethyl ether or dimethyoxyethane; an ester such as methyl acetate or ethyl acetate; an alcohol such as methanol, ethanol, propanol or tert-butanol; a nitrile such as acetonitrile, propionitrile or acrylonitrile; and a ketone such as acetone or methyl ethyl ketone.

[0098] Methyl iodide in reaction (O) is used in an amount of from 1 to 10 mols, preferably from 1 to 3 mols, per mol of the compound of the formula (XV). Further, methyl iodide may serve also as a solvent if used excessively.

[0099] The reaction temperature for reaction (O) is usually from 0 to 100° C., preferably from 10 to 50° C. The reaction time is usually from 0.5 to 48 hours, preferably from 1 to 24 hours.

[0100] The compound of the formula (XIV) to be used in the above reaction (N) is novel and can be produced by the following reaction (P).

[0101] In reaction (P), A, R1 and R2 are as defined above, U is an atom of chlorine or bromine.

[0102] Reaction (P) is carried out in the presence of an azidation agent. The azidation agent may be one or more suitably selected from e.g. sodium azide, potassium azide and trimethylsilyl azide.

[0103] Reaction (P) is carried out usually in the presence of a solvent. The solvent may be any solvent so long as it is a solvent inert to the reaction. For example, it may be one or more suitably selected from e.g. an aromatic hydrocarbon such as benzene, toluene, xylene or chlorobenzene; an aliphatic hydrocarbon such as carbon tetrachloride, methyl chloride, chloroform, dichloromethane, dichloroethane, trichloroethane, hexane or cyclohexane; an ether such as dioxane, tetrahydrofuran, diethyl ether or dimethoxyethane; an ester such as methyl acetate or ethyl acetate; a polar aprotic solvent such as dimethyl sulfoxide, sulfolane, dimethylacetamide, dimethylformamide, N-methylpyrrolidone or pyridine; a nitrile such as acetonitrile, propionitrile or acrylonitrile; a ketone such as acetone or methyl ethyl ketone; an alcohol such as methanol, ethanol, propanol or tert-butanol; and water.

[0104] The reaction temperature for reaction (P) is usually from 0 to 150° C., preferably from 20 to 90° C. The reaction time is usually from 0.1 to 96 hours, preferably from 0.5 to 12 hours.

[0105] The compound of the formula (XV) to be used in the above reaction (O) is novel and can be produced by the following reaction (Q).

[0106] In reaction (Q), A, R1 and R2 are as defined above.

[0107] Reaction (Q) can be carried out in accordance with a common hydrazone synthetic reaction and, if necessary, in the presence of a dehydrating agent and/or a catalyst.

[0108] As the dehydrating agent, molecular sieve may, for example, be mentioned. The dehydrating agent may be used usually from 1 to 30 times, preferably from 5 to 10 times relative to the weight of the compound of the formula (XII).

[0109] The catalyst may, for example, be titanium tetrachloride.

[0110] Dimethylhydrazine for reaction (Q) is used usually in an amount of from 1 to 30 mols, preferably from 5 to 10 mols, per mol of the compound of the formula (XII).

[0111] The reaction temperature for reaction (Q) is usually from 20 to 150° C., preferably from 50 to 120° C. The reaction time is usually from 5 to 200 hours, preferably from 24 to 120 hours.

[0112] The compound of the formula (XVI) to be used in the above reaction (P) is novel and can be produced by the following reaction (R).

[0113] In reaction (R), A, R1, R2 and U are as defined above.

[0114] Reaction (R) is carried out in the presence of a chlorination agent or a bromination agent. The chlorination agent may be one or more suitably selected from e.g. chlorine and N-chlorosuccinimide. The bromination agent may be one or more suitably selected from e.g. bromine, N-bromosuccinimide and phenyltrimethyl ammonium tribromide.

[0115] Reaction (R) is carried out usually in the presence of a solvent. The solvent may be any solvent so long as it is a solvent inert to the reaction. For example, it may be one or more suitably selected from e.g. an aromatic hydrocarbon such as benzene, toluene, xylene or chlorobenzene; an aliphatic hydrocarbon such as carbon tetrachloride, methyl chloride, chloroform, dichloromethane, dichloroethane, trichloroethane, hexane or cyclohexane; an ether such as dioxane, tetrahydrofuran, diethyl ether or dimethoxyethane; an ester such as methyl acetate or ethyl acetate; a polar aprotic solvent such as dimethyl sulfoxide, sulfolane, dimethylacetamide, dimethylformamide, N-methylpyrrolidone or pyridine; an organic acid such as acetic acid or propionic acid; and water.

[0116] Reaction (R) is carried out, if necessary, in the presence of a base or an acid.

[0117] The base may, for example, be lithium diisopropylamide. The base is used in an amount of from 1 to 2 mols, preferably from 1 to 1.2 mols, per mol of the compound of the formula (XII).

[0118] The acid may be one or more suitably selected from e.g. an organic acid such as acetic acid or propionic acid, and aluminum chloride. The acid is usually used in a catalytic amount. Further, an organic acid as a solvent may serve as both a solvent and an acid if used excessively.

[0119] The reaction temperature for reaction (R) is usually from −100 to 150° C., preferably from −78 to 110° C. The reaction time is usually from 0.1 to 48 hours, preferably from 0.5 to 24 hours. However, if it is carried out in the presence of a base, the reaction temperature is usually from −100 to 0° C., preferably from −78 to −20° C., and the reaction time is usually from 0.1 to 12 hours, preferably from 0.5 to 6 hours. If it is carried out in the presence of an acid, the reaction temperature is usually from 0 to 150° C., preferably from 20 to 110° C., and the reaction time is usually from 0.1 to 48 hours, preferably from 1 to 24 hours.

[0120] The compound of the formula (XII) to be used in the above reaction (Q) is a known compound, or can be produced by the following reactions (S) to (T) or by methods in accordance therewith.

[0121] In reaction (S), R1 and R2 are as defined above, and Z is an oxygen atom or —C(G1)G2-, Xa is an hydrogen atom, chlorine atom or alkyl, Xa′ is a chlorine atom or alkyl, each of Xb, Xc, Xd, Xe, G1 and G2 is an atom of hydrogen, fluorine or chlorine, V is an atom of bromine or iodine, and j is 0 or 1.

[0122] The first step in reaction (S) is carried out in the presence of a base and a solvent.

[0123] The base may be suitably selected from an organic lithium compound such as lithium diisopropylamide. The base is used in an amount of from 1 to 2 mols, preferably from 1 to 1.5 mols, per mol of the compound of the formula (XVII).

[0124] The solvent may be any solvent so long as it is a solvent inert to the reaction. For example, it may be one or more suitably selected from e.g. an ether such as dioxane, tetrahydrofuran and diethyl ether.

[0125] The chlorination agent to be used for the first step in reaction (S) may, for example, be N-chlorosuccinimide.

[0126] The formula: Xa′-I to be used for the first step in reaction (S) is used in an amount of from 1 to 10 mols, preferably from 1 to 5 mols, per mol of the compound of the formula (XVII). Further, the chlorination agent to be used for the first step in reaction (S) is used in an amount of from 1 to 5 mols, preferably from 1 to 3 mols, per mol of the compound of the formula (XVII).

[0127] The first step in reaction (S) is carried out, if necessary, in the presence of an inert gas. The inert gas may be suitably selected from e.g. nitrogen gas or argon gas.

[0128] The reaction temperature for the first step in reaction (S) is usually from −100 to 50° C., preferably from −70 to 25° C. The reaction time is usually from 1 to 48 hours, preferably from 1 to 20 hours.

[0129] The second step in reaction (S) is carried out, usually in the presence of a base and a solvent.

[0130] The base may be one or more suitably selected from e.g. organic lithium compounds such as methyllithium and n-butyllithium. The base is used in an amount of from 1 to 2 mols, preferably from 1 to 1.5 mols, per mol of the compound of the formula (XVII) or (XVIII).

[0131] The solvent may be any solvent so long as it is a solvent inert to the reaction. For example, it may be one or more suitably selected from e.g. ethers such as dioxane, tetrahydrofuran and diethyl ether.

[0132] The compound of the formula (XIX) to be used for the second step in reaction (S) is used in an amount of from 1 to 3 mols, preferably from 1 to 1.5 mols, per mol of the compound of the formula (XVII) or (XVIII).

[0133] The second step in reaction (S) is carried out, if necessary, in the presence of an inert gas. The inert gas may be suitably selected from e.g. nitrogen gas and argon gas.

[0134] The reaction temperature for the second step in reaction (S) is usually from −100 to 50° C., preferably from −70 to 25° C. The reaction time is usually from 1 to 48 hours, preferably from 1 to 20 hours.

[0135] In reaction (T), R1, R2, Z, Xa, Xa′, Xb, Xc, Xd, Xe, V and j are as defined above.

[0136] The first step in reaction (T) is carried out usually in the presence of a base and a solvent.

[0137] The base may be one or more suitably selected from e.g. organic lithium compounds such as methyllithium and n-butyllithium.

[0138] The base is used in an amount of from 1 to 2 mols, preferably from 1 to 1.5 mols, per mol of the compound of the formula (XVII) or (XVIII).

[0139] The solvent may be any solvent so long as it is a solvent inert to the reaction. For example, it may be one or more suitably selected from e.g. an ether such as dioxane, tetrahydrofuran and diethyl ether.

[0140] The compound of the formula (XX) to be used for the first step in reaction (T) is used in an amount of from 1 to 3 mols, preferably from 1 to 1.5 mols, per mol of the compound of the formula (XVII) or (XVIII).

[0141] The first step in reaction (T) is carried out, if necessary, in the presence of an inert gas. The inert gas may be suitably selected from e.g. nitrogen gas and argon gas.

[0142] The reaction temperature for the first step in reaction (T) is usually from −100 to 50° C., preferably from −70 to 25° C. The reaction time is usually from 1 to 48 hours, preferably from 1 to 20 hours.

[0143] The second step for reaction (T) is carried out usually in the presence of an oxidizing agent and a solvent.

[0144] The oxidizing agent may be one or more suitably selected from e.g. pyridinium chlorochromate and manganese dioxide. The oxidizing agent is used in an amount of from 1 to 10 mols, preferably from 1 to 3 mols, per mol of the compound of the formula (XXI).

[0145] The solvent may be any solvent so long as it is a solvent inert to the reaction. For example, it may be one or more suitably selected from e.g. an aromatic hydrocarbon such as benzene, toluene, xylene or chlorobenzene; and an aliphatic hydrocarbon such as carbon tetrachloride, methyl chloride, chloroform, dichloromethane, dichloroethane, trichloroethane, hexane or cyclohexane.

[0146] The reaction temperature for the second step in reaction (T) is usually from 0 to 150° C., preferably from to 100° C. The reaction time is usually from 0.5 to 24 hours, preferably from 1 to 12 hours.

[0147] Preferred embodiments of pesticides containing the compounds of the present invention will now be described.

[0148] The pesticides containing the compounds of the present invention are particularly useful as an insecticide, a miticide, a nematicide and a soil pesticide, and they are effective for controlling plant parasitic mites such as two-spotted spider mite (Tetranychus urticae), carmine spider mite (Tetranychus cinnabarinus), kanzawa spider mite (Tetranychus kanzawai), citrus red mite (Panonychus citri), European red mite (Panonychus ulmi), broad mite (Polyphagotarsonemus latus), pink citrus rust mite (Aculops pelekassi) and bulb mite (Rhizoglyphus echinopus); agricultural insect pests such as aphids such as green peach aphid (Myzus persicae) and cotton aphid (Aphis gossypii), diamondback moth (Plutella xylostella), cabbage armyworm (Mamestra brassicae), common cutworm (Spodoptera litura), codling moth (Laspeyresia pomonella), bollworm (Heliothis zea), tobacco budworm (Heliothis virescens), gypsy moth (Lymantria dispar), rice leafroller (Cnaphalocrocis medinalis), Adoxophyes sp., colorado potato beetle (Leptinotarsa decemlineata), cucurbit leaf beetle (Aulacophora femoralis), boll weevil (Anthonomus grandis), planthoppers, leafhoppers, scales, bugs, whiteflies, thrips, grasshoppers, anthomyiid flies, scarabs, black cutworm (Agrotis ipsilon), cutworm (Agrotis segetum) and ants; plant parasitic nematodes such as root-knot nematodes, cyst nematodes, root-lesion nematodes, rice white-tip nematode (Aphelenchoides besseyi), strawberry bud nematode (Nothotylenchus acris), pine wood nematode (Bursaphelenchus lignicolus); gastropods such as slugs and snails; soil pests such as isopods such as pillbugs (Armadilidium vulgare) and pillbugs (Porcellio scaber); hygienic insect pests such as tropical rat mite (Ornithonyssus bacoti), cockroachs, housefly (Musca domestica) and house mosquito (Culex pipiens); stored grain insect pests such as angoumois grai moth (Sitotroga cerealella), adzuki bean weevil (Callosobruchus chinensis), red flour beetle (Tribolium castaneum) and mealworms; household goods insect pests such as casemaking clothes moth (Tinea pellionella), black carpet beetle (Anthrenus scrophularidae) and subterranean termites; domestic mites such as mold mite (Tyrophagus putrescentiae), Dermatophagoides farinae and Chelacaropsis moorei. Among them, the pesticides containing the compounds of the present invention are particularly effective for controlling agricultural insect pests, plant parasitic nematodes or the like. Further, they are effective against insect pests having acquired resistance to organophosphorus, carbamate and/or synthetic pyrethroid insecticides. Moreover, the compounds of the present invention have excellent systemic properties, and by the application of the compounds of the present invention to soil treatment, not only noxious insects, noxious mites, noxious nematodes, noxious gastropods and noxious isopods in soil but also foliage pests can be controlled.

[0149] Another preferred embodiments of the pesticides containing compounds of the present invention may be agricultural and horticultural pesticides which collectively control the above-mentioned plant parasitic mites, agricultural insect pests, plant parasitic nematodes, gastropods and soil pests.

[0150] The pesticide containing the compound of the present invention, is usually formulated by mixing the compound with various agricultural adjuvants and used in the form of a formulation such as a dust, granules, water-dispersible granules, a wettable powder, a water-based suspension concentrate, an oil-based suspension concentrate, water soluble granules, an emulsifiable concentrate, a soluble concentrate, a paste, an aerosol or an ultra low-volume formulation. However, so long as it is suitable for the purpose of the present invention, it may be formulated into any type of formulation which is commonly used in this field. Such agricultural adjuvants include solid carriers such as diatomaceous earth, slaked lime, calcium carbonate, talc, white carbon, kaoline, bentonite, a mixture of kaolinite and sericite, clay, sodium carbonate, sodium bicarbonate, mirabilite, zeolite and starch; solvents such as water, toluene, xylene, solvent naphtha, dioxane, acetone, isophorone, methyl isobutyl ketone, chlorobenzene, cyclohexane, dimethylsulfoxide, dimethylformamide, dimethylacetamide, N-methyl-2-pyrrolidone, and alcohol; anionic surfactants and spreaders such as a salt of fatty acid, a benzoate, an alkylsulfosuccinate, a dialkylsulfosuccinate, a polycarboxylate, a salt of alkylsulfuric acid ester, an alkyl sulfate, an alkylaryl sulfate, an alkyl diglycol ether sulfate, a salt of alcohol sulfuric acid ester, an alkyl sulfonate, an alkylaryl sulfonate, an aryl sulfonate, a lignin sulfonate, an alkyldiphenyl ether disulfonate, a polystyrene sulfonate, a salt of alkylphosphoric acid ester, an alkylaryl phosphate, a styrylaryl phosphate, a salt of polyoxyethylene alkyl ether sulfuric acid ester, a polyoxyethylene alkylaryl ether sulfate, a salt of polyoxyethylene alkylaryl ether sulfuric acid ester, a polyoxyethylene alkyl ether phosphate, a salt of polyoxyethylene alkylaryl phosphoric acid ester, and a salt of a condensate of naphthalene sulfonate with formalin; nonionic surfactants and spreaders such as a sorbitan fatty acid ester, a glycerin fatty acid ester, a fatty acid polyglyceride, a fatty acid alcohol polyglycol ether, acetylene glycol, acetylene alcohol, an oxyalkylene block polymer, a polyoxyethylene alkyl ether, a polyoxyethylene alkylaryl ether, a polyoxyethylene styrylaryl ether, a polyoxyethylene glycol alkyl ether, a polyoxyethylene fatty acid ester, a polyoxyethylene sorbitan fatty acid ester, a polyoxyethylene glycerin fatty acid ester, a polyoxyethylene hydrogenated castor oil, and a polyoxypropylene fatty acid ester; and vegetable and mineral oils such as olive oil, kapok oil, castor oil, palm oil, camellia oil, coconut oil, sesame oil, corn oil, rice bran oil, peanut oil, cottonseed oil, soybean oil, rapeseed oil, linseed oil, tung oil, and liquid paraffins. Such adjuvants may be selected for use among those known in this field, so long as the purpose of the present invention can thereby be accomplished. Further, various additives which are commonly used, such as a filler, a thickener, an anti-settling agent, an anti-freezing agent, a dispersion stabilizer, a phytotoxicity reducing agent, and an anti-mold agent, may also be employed.

[0151] The weight ratio of the compound of the present invention to the various agricultural adjuvants is usually from 0.001:99.999 to 95:5, preferably from 0.005:99.995 to 90:10.

[0152] In the actual application of such a formulation, it may be used as it is, or may be diluted to a predetermined concentration with a diluent such as water, and various spreaders may be added thereto, as the case requires.

[0153] The application of the pesticide containing the compound of the present invention can not generally be defined, as it varies depending upon the weather conditions, the type of the formulation, the application season, the application site or the types or degree of outbreak of the pest insects. However, it is usually applied in a concentration of the active ingredient being from 0.05 to 800,000 ppm, preferably from 0.5 to 500,000 ppm, and the dose per unit area is such that the compound of the present invention is from 0.05 to 50,000 g, preferably from 1 to 30,000 g, per hectare. Further, agricultural and horticultural pesticides as another preferred embodiment of pesticides containing the compounds of the present invention may be applied in accordance with the above-described application of pesticides. The present invention includes such a method for controlling pests, particularly for controlling agricultural insect pests or plant parasitic nematodes by such applications.

[0154] Various formulations of pesticides containing the compounds of the present invention or their diluted compositions may be applied by conventional methods for application which are commonly employed, such as spraying (e.g. spraying, jetting, misting, atomizing, powder or grain scattering or dispersing in water), soil application (e.g. mixing or drenching), surface application (e.g. coating, powdering or covering) or impregnation to obtain poisonous feed. Further, it is possible to feed domestic animals with a food containing the above active ingredient and to control the outbreak or growth of pests, particularly insect pests, with their excrements. Furthermore, the active ingredient may also be applied by a so-called ultra low-volume application method. In this method, the composition may be composed of 100% of the active ingredient.

[0155] Further, the pesticides containing compounds of the present invention may be mixed with or may be used in combination with other agricultural chemicals, fertilizers or phytotoxicity-reducing agents, whereby synergistic effects or activities may sometimes be obtained. Such other agricultural chemicals include, for example, a herbicide, an insecticide, a miticide, a nematicide, a soil pesticide, a fungicide, an antivirus agent, an attractant, an antibiotic, a plant hormone and a plant growth regulating agent. Especially, with a mixed pesticide having a compound of the present invention mixed with or used in combination with one or more active compounds of other agricultural chemicals, the application range, the application time, the pesticidal activities, etc. may be improved to preferred directions. The compound of the present invention and the active compounds of other agricultural chemicals may separately be formulated so that they may be mixed for use at the time of application, or they may be formulated together. The present invention includes such a mixed pesticidal composition.

[0156] The mixing ratio of the compound of the present invention to the active compounds of other agricultural chemicals can not generally be defined, since it varies depending upon the weather conditions, the types of formulations, the application time, the application site, the types or degree of outbreak of insect pests, etc., but it is usually within a range of from 1:300 to 300:1, preferably from 1:100 to 100:1, by weight. Further, the dose for the application is such that the total amount of the active compounds is from 0.1 to 50,000 g, preferably from 1 to 30,000 g, per hectare. The present invention includes a method for controlling pests by an application of such a mixed pesticide composition.

[0157] The active compounds of pest control agents such as insecticides, miticides, nematicides or soil pesticides in the above-mentioned other agricultural chemicals, include, for example, (by common names, some of them are still in an application stage) organic phosphate compounds such as Profenofos, Dichlorvos, Fenamiphos, Fenitrothion, EPN, Diazinon, Chlorpyrifos-methyl, Acephate, Prothiofos, Fosthiazate, Phosphocarb, Cadusafos, Disulfoton, Chlorpyrifos, Demeton-S-methyl, Dimethoate, and Methamidophos; carbamate compounds such as Carbaryl, Propoxur, Aldicarb, Carbofuran, Thiodicarb, Methomyl, Oxamyl, Ethiofencarb, Pirimicarb, Fenobucarb, Carbosulfan, and Benfuracarb; nereistoxin derivatives such as Cartap, Thiocyclam and Bensultap; organic chlorine compounds such as Dicofol, and Tetradifon; organometallic compounds such as Fenbutatin Oxide; pyrethroid compounds such as Fenvalerate, Permethrin, Cypermethrin, Deltamethrin, Cyhalothrin, Tefluthrin, Ethofenprox and Bifenthrin; benzoylurea compounds such as Diflubenzuron, Chlorfluazuron, Teflubenzuron, Flufenoxuron, Lufenuron, and Novaluron; juvenile hormone-like compounds such as Methoprene, Pyriproxyfen, and Fenoxycarb; pyridazinone compounds such as Pyridaben; pyrazole compounds such as Fenpyroximate, Fipronil, Tebufenpyrad, Ethiprole, Tolfenpyrad, and Acetoprole; neonicotinoids such as Imidacloprid, Nitenpyram, Acetamiprid, Thiacloprid, Thiamethoxam, Clothianidin, and Dinotefuran; hydrazine compounds such as Tebufenozide, Methoxyfenozide, and Chromafenozide; dinitro compounds; organic sulfur compounds; urea compounds; triazine compounds; hydrazone compounds; and other compounds, such as Flonicamid, Buprofezin, Hexythiazox, Amitraz, Chlordimeform, Silafluofen, Triazamate, Pymetrozine, Pyrimidifen, Chlorfenapyr, Indoxacarb, Acequinocyl, Etoxazole, Cyromazine, 1,3-dichloropropene, Diafenthiuron, Benclothiaz, Flufenerim, Pyridalyl, and Spirodiclofen. Further, microbial agricultural chemicals such as BT agents, insect viruses, entomopathogenic fungi, and nematophagous fungi or antibiotics such as Avermectin, Milbemectin, Spinosad, Ivermectin, and Emamectin-benzoate may be used in admixture or in combination.

[0158] The active compounds of fungicides among the above-mentioned other agricultural chemicals include, for example, (by common names, some of which are still in an application stage) pyrimidinamine compounds such as Mepanipyrim, Pyrimethanil, and Cyprodinil; azole compounds such as Triadimefon, Bitertanol, Triflumizole, Etaconazole, Propiconazole, Penconazole, Flusilazole, Myclobutanil, Cyproconazole, Terbuconazole, Hexaconazole, Furconazole-cis, Prochloraz, Metconazole, Epoxiconazole, Tetraconazole, Oxpoconazole, and Sipconazole; quinoxaline compounds such as Quinomethionate; dithiocarbamate compounds such as Maneb, Zineb, Mancozeb, Polycarbamate, Propineb; organic chlorine compounds such as Fthalide, Chlorothalonil, and Quintozene; imidazole compounds such as Benomyl, Thiophanate-Methyl, Carbendazim, and Cyazofamid; pyridinamine compounds such as Fluazinam; cyanoacetamide compounds such as Cymoxanil; phenylamide compounds such as Metalaxyl, Oxadixyl, Ofurace, Benalaxyl, Furalaxyl, and Cyprofuram; sulfenic acid compounds such as Dichlofluanid; copper compounds such as cupric hydroxide, and Oxine Copper; isoxazole compounds such as Hydroxyisoxazole; organophosphorus compounds such as Fosetyl-Al, Tolclofos-Methyl, S-benzyl O,O-diisopropylphosphorothioate, O-ethyl S,S-diphenylphosphorodithioate, and aluminumethylhydrogen phosphonate; N-halogenothioalkyl compounds such as Captan, Captafol, and Folpet; dicarboximide compounds such as Procymidone, Iprodione, and Vinclozolin; benzanilide compounds such as Flutolanil, Mepronil, and Zoxamide; piperazine compounds such as Triforine; pyrizine compounds such as Pyrifenox; carbinol compounds such as Fenarimol; and Flutriafol; piperidine compounds such as Fenpropidine; morpholine compounds such as Fenpropimorph; organotin compounds such as Fentin Hydroxide, and Fentin Acetate; urea compounds such as Pencycuron; cinnamic acid compounds such as Dimethomorph; phenylcarbamate compounds such as Diethofencarb; cyanopyrrole compounds such as Fludioxonil, and Fenpiclonil; Strobilurin compounds such as Azoxystrobin, Kresoxim-Methyl, Metominofen, Trifloxystrobin, and Picoxystrobin; oxazolidinedione compounds such as Famoxadone; thiazole carboxamide compounds such as Ethaboxam; silyl amide compounds such as Silthiopham; aminoacid amidecarbamate compounds such as Iprovalicarb; imidazolidine compound such as Fenamidone; hydroxyanilide compounds such as Fenhexamid; benzene sulfonamide compounds such as Flusulfamide; Strobilurin compounds such as Pyraclostrobin; anthraquinone compounds; crotonic acid compounds; antibiotics; and other compounds, such as Isoprothiolane, Tricyclazole, Pyroquilon, Diclomezine, Pro. benazole, Quinoxyfen, Propamocarb Hydrochloride, Spiroxamine, Chloropicrin, Dazomet, and Metam-Sodium.

[0159] Further, agricultural chemicals which may be used in admixture with or in combination with the compounds of the present invention, may, for example, be the active ingredient compounds in the herbicides as disclosed in Farm Chemicals Handbook (1998 edition), particularly those of soil treatment type.

[0160] Further, pesticides containing the compounds of the present invention are useful as agents for controlling parasites on animals, particularly as agents for controlling parasites in the bodies of animals, or as agents for controlling animal diseases caused by such parasites.

[0161] For example, they are effective for controlling (1) parasites parasitic on the exterior of a host animal, such as, acarus such as mange mite, mesostigmatid mites, sarcoptic mange mite (Sarcoptes scabiei), trombiculid mites, New Zealand cattle tick (Haemaphyalis longicornis) and southern cattle tick (Boophilus microplus); fleas such as cat flea (Ctenocephalides felis), dog flea (Ctenocephalides canis), northern rat flea (Nosopsyllus fasciatus), oriental rat flea (Xenopsylla cheopis) and human flea (Pulex irritans); sucking lice such as short-nosed cattle louse (Haematopinus eurysternus), horse sucking louse (Haematopinus asini), sheep lice, long-nosed cattle louse (Linognathus vituli) and head louse (Pediculus capitis); biting lice such as dog biting louse (Trichodectes canis); blood-sucking dipterous insects such as horse fly (Tabanus trigonus), biting midges (Culicoides schultzei) and blackfly (Simulium ornatum); and (2) parasites parasitic in the body of a host animal, such as, nematodes such as lung worms, whipworm (Trichuris trichiura), tuberous worm, gastric parasites, ascaris and filarioidea; tapeworms; flukes; and protozoa such as coccidia, malarial parasite (Plasmodium malariae), intestinal sarcocyst, Toxoplasma and cryptosporidium.

[0162] The compound of the present invention is usually formulated together with a suitable vehicle into a formulation such as a powder, a granule, a parvule, a tablet, a dusting powder, a capsule, a solution or an emulsion. The suitable vehicle may be one which is commonly used as a feed additive, and it may, for example, be lactose, sucrose, glucose, starch, wheat powder, corn powder, soybean meal, degreased rice bran, calcium carbonate or other commercially available feed material. Further, the compound of the present invention can be used, together with a vehicle, in combination with various vitamins, minerals, amino acids, enzyme drugs, antifebriles, sedatives, antiphlogistics, bactericides, colorants, aromatizing agents, preservatives, etc. The dose of the compound of the present invention varies depending upon the parasites as the object of control, the administration method, the purpose of administration, the diseased degree, etc. However, it is usually administered as mixed in a feed in a concentration of at least 0.1 ppm.

[0163] The compound of the present invention exhibits an effect for controlling parasites on animals, such as fleas, coccidia and filarioidea, by a test in accordance with the test method disclosed in e.g. JP-A-5-70350 or JP-A-11-500439.

[0164] Preferred embodiments in the present invention are as follows. However, it should be understood that the present invention is by no means restricted to such specific embodiments.

[0165] (1) An acid amide derivative of the above formula (I) or a salt thereof, wherein A is phenyl which may be substituted by X′; benzyl which may be substituted by X, naphthyl which may be substituted by X, a heterocyclic group which may be substituted by X, a fused heterocyclic group which may be substituted by X, indanyl (the indanyl may be substituted by halogen, alkyl or alkoxy) or tetrahydronaphthyl (the tetrahydronaphthyl may be substituted by halogen, alkyl or alkoxy), X′ is alkoxyalkoxy, haloalkoxyalkoxy, alkoxyhaloalkoxy, haloalkoxyhaloalkoxy, phenyl which may be substituted by Y′, phenoxy which may be substituted by Y′, benzyloxy which may be substituted by Y′, pyridyloxy which may be substituted by Y′, —OR4, —SR5, —NR6R7, —CO2R8, —C(═O)NR9R10 or an unsaturated heterocyclic group (the unsaturated heterocyclic ring may be substituted by halogen, alkyl, haloalkyl, alkoxy or haloalkoxy), Y′ is —OR4, —CO2R11, —CONR12R13 or an unsaturated heterocyclic group (the unsaturated heterocyclic ring may be substituted by halogen, alkyl, haloalkyl, alkoxy or haloalkoxy).

[0166] (2) The acid amide derivative or a salt thereof according to the above (1), wherein A is phenyl which may be substituted by X′.

[0167] (3) The acid amide derivative or a salt thereof according to the above (1), wherein A is benzyl which may be substituted by X, naphthyl which may be substituted by X, a heterocyclic group which may be substituted by X, a fused heterocyclic group which may be substituted by X, indanyl (the indanyl may be substituted by halogen, alkyl or alkoxy), or tetrahydronaphthyl (the tetrahydronaphthyl may be substituted by halogen, alkyl or alkoxy).

[0168] (4) The acid amide derivative or a salt thereof according to the above (3), wherein A is benzyl which may be substituted by X, naphthyl which may be substituted by X.

[0169] (5) The acid amide derivative or a salt thereof according to the above (3), wherein A is a heterocyclic group which may be substituted by X, or a fused heterocyclic group which may be substituted by X.

[0170] (6) The acid amide derivative or a salt thereof according to the above (5), wherein the heterocyclic group is a 5- or 6-membered heterocyclic group containing from 1 to 4 atoms of at least one type selected from the group consisting of O, S and N, and the fused heterocyclic group is a 8- to 10-membered fused heterocyclic group containing from 1 to 4 atoms of at least one type selected from the group consisting of O, S and N.

[0171] (7) The acid amide derivative or a salt thereof according to the above (6), wherein the heterocyclic group is furyl, tetrahydrofuryl, thienyl, pyrrolyl, pyrrolinyl, pyrrolidinyl, dioxolanyl, oxazolyl, isoxazolyl, thiazolyl, isothiazolyl, imidazolyl, imidazolinyl, imidazolidinyl, pyrazolyl, pyrazolinyl, pyrazolidinyl, triazolyl, oxadiazolyl, thiadiazolyl, tetrazolyl, pyranyl, pyridyl, piperidinyl, dioxanyl, oxazinyl, morpholinyl, thiazinyl, pyridazinyl, pyrimidinyl, pyrazinyl, piperazinyl or triazinyl, and the fused heterocyclic group is benzofuranyl, isobenzofuranyl, dihydrobenzofuranyl, dihydroisobenzofuranyl, benzothienyl, isobenzothienyl, dihydrobenzothienyl, dihydroisobenzothienyl, tetrahydrobenzothienyl, indolyl, isoindolyl, benzoxazolyl, benzothiazolyl, indazolyl, benzimidazolyl, benzodioxolanyl, benzodioxanyl, chromenyl, chromanyl, isochromanyl, chromonyl, chromanonyl, quinolyl, isoquinolyl, cinnolinyl, phthalazinyl, quinazolinyl, quinoxalinyl, indolizinyl, quinolizinyl, imidazopyridyl, naphthyridinyl, pteridinyl, dihydrobenzoxazinyl, dihydrobenzoxazolinonyl, dihydrobenzoxazinonyl or benzothioxanyl.

[0172] (8) The acid amide derivative or a salt thereof according to the (3), wherein A is indanyl (the indanyl may be substituted by halogen, alkyl or alkoxy), or tetrahydronaphthyl (the tetrahydronaphthyl may be substituted by halogen, alkyl or alkoxy).

[0173] (9) The acid amide derivative or a salt thereof according to the above (1) or (3) to (7), wherein X is at least one type selected from the group consisting of halogen, alkyl, haloalkyl, alkoxy or haloalkoxy.

[0174] (10) The acid amide derivative or a salt thereof according to the above (1) to (8), wherein B is phenyl which may be substituted by Y.

[0175] (11) The acid amide derivative or a salt thereof according to the above (1) to (8), wherein each of R1 and R2 is alkyl, R3 is a hydrogen atom.

[0176] (12) The acid amide derivative or a salt thereof according to the above (1) to (8), wherein B is phenyl which may be substituted by Y, each of R1 and R2 is alkyl, and R3 is a hydrogen atom.

[0177] (13) The acid amide derivative or a salt thereof according to the above (10) or (12), wherein Y is at least one type selected from the group consisting of halogen, alkyl or haloalkyl.

[0178] Further, other preferred embodiments in the present invention are as follows. However, the present invention is not limited to them.

[0179] An acid amid derivative of the above formula (I) or a salt thereof, wherein A is phenyl which may be substituted by X, benzyl which may be substituted by X, naphthyl which may be substituted by X, a heterocyclic group which may be substituted by X, or a fused heterocyclic group which may be substituted by X, B is alkyl, cycloalkyl, phenyl which may be substituted by Y, a heterocyclic group which may be substituted by Y, or a fused heterocyclic group which may be substituted by Y, X is halogen, alkyl, haloalkyl, alkenyl, haloalkenyl, alkynyl, haloalkynyl, alkoxy, haloalkoxy, alkenyloxy, haloalkenyloxy, alkynyloxy, haloalkynyloxy, alkylthio, haloalkylthio, alkenylthio, haloalkenylthio, alkynylthio, haloalkynylthio, alkylsulfinyl, haloalkylsulfinyl, alkylsulfonyl, haloalkylsulfonyl, dialkylaminosulfonyl, nitro, cyano, phenyl which may be substituted by Y, phenoxy which may be substituted by Y, benzyloxy which may be substituted by Y, pyridyloxy which may be substituted by Y, —OR4, —SR5, —NR6R7, —CO2R8, —C(═O)NR9R10 or an unsaturated heterocyclic group (the unsaturated heterocyclic ring may be substituted by halogen, alkyl, haloalkyl, alkoxy or haloalkoxy), Y is halogen, alkyl, haloalkyl, alkoxy, haloalkoxy, alkylthio, haloalkylthio, alkylsulfinyl, haloalkylsulfinyl, alkylsulfonyl, haloalkylsulfonyl, dialkylaminosulfonyl, nitro, cyano, —CO2R11, —CONR12R13 or an unsaturated heterocyclic group (the unsaturated heterocyclic ring may be substituted by halogen, alkyl, haloalkyl, alkoxy or haloalkoxy), each of R1 and R2 is alkyl, cyano or —CO2R14, or R1 and R2 may together form a 3- to 6-membered saturated carbocyclic ring, R3 is hydrogen, alkyl, alkoxyalkyl, alkylthioalkyl, —COR15, —S(O)mR16 or —S(O)nNR17R18, each of R4 and R6 is hydrogen, —C(═W)R19, —C(═W)OR20, —C(═W)SR21, —C(═W)NR22 R23, —S(O)qR24 or —S(O)rNR25R26, R5 is hydrogen, —C(═W)R19, —C(═W)OR20, —C(═W)SR21 or —C(═W)NR22R23, R7 is hydrogen, alkyl or haloalkyl, each of R8, R9, R10, R11, R12, R13 and R14 is hydrogen or alkyl, R15 is hydrogen, alkyl or alkoxy, each of R16, R17, R18, R19, R20, R21, R22, R23, R24 , R25 and R26 is alkyl, haloalkyl or phenyl (the phenyl which may be substituted by halogen, alkyl, haloalkyl, alkoxy or haloalkoxy), each of m, n, q and r is from 0 to 2, W is oxygen or sulfur.

[0180] Now, Examples of the present invention will be described. However, it should be understood that the present invention is by no means restricted to such specific Examples. Firstly, Preparation Examples for the compounds of the present invention will be described.

PREPARATION EXAMPLE 1

[0181] Preparation of 2-hydroxycarbonyl-N-[(4′-chloro-1,1-dimethyl)phenacyl]benzamide (The after-mentioned Compound No. 1-120)

[0182] 0.83 g of triethylamine was added to a mixture comprising 1.92 g of α-amino-4-chloroisobutyrophenone hydrochloride and 20 ml of tetrahydrofuran at room temperature, and a mixed solution of 1.21 g of phthalic anhydride and 30 ml of tetrahydrofuran was added thereto, followed by a reaction at room temperature for 16 hours. After completion of the reaction, the reaction mixture was concentrated, and 70 ml of water was added to the residue, followed by acidification by 10% hydrochloric acid, and then by stirring for 30 minutes. The precipitated crystal was collected by filtration, washed with water, dissolved in ethyl acetate, and then dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure to obtain 1.84 g of the desired product having a melting point of from 212 to 214° C. The NMR spectrum data of this product were as follows.

[0183]

1
H-NMR δppm (Solvent: DMSO/400 MHz) 1.53(s, 6H),7.00(d, 1H),7.48(t, 1H),7.52-7.55(m, 3H),7.75(d, 1H),8.05(d, 2H),9.11(s, 1H),12.96(brs, 1H).

PREPARATION EXAMPLE 2

[0184] Preparation of 2-(3-thienyl)-N-[(4′-chloro-1,1-dimethyl)phenacyl]benzamide (The after-mentioned Compound No. 1-80)

[0185] 0.24 g of 3-thiopheneboric acid, 0.51 g of sodium carbonate, 5 ml of water and 0.1 g of tetrakis(triphenylphosphine)palladium(0) were added to a mixed solution comprising 0.35 g of 2-bromo-N-[(4′-chloro-1,1-dimethyl)phenacyl]benzamide and 5 ml of 1,2-dimethoxyethane, followed by a reaction under heating and refluxing for 8 hours under nitrogen atmosphere. After completion of the reaction, the reaction mixture was allowed to cool and added to 40 ml of water, then 20 ml of t-butyl methyl ether was added and stirred, followed by neutralization with 30% sulfuric acid, and then by extraction with ethyl acetate. The organic layer was washed with an aqueous sodium chloride solution, then dried over anhydrous sodium sulfate, followed by concentration under reduced pressure. The obtained residue was purified by silica gel column chromatography (eluent: ethyl acetate/n-hexane=3/7) to obtain 0.14 g of the desired product having a melting point of from 170 to 173° C. The NMR spectrum data of this product were as follows.

[0186]

1
H-NMR δppm (Solvent: CDCl3/400 MHz) 1.48(s, 6H),6.09(brs, 1H),7.13(dd, 1H),7.32-7.48(m, 8H), 7.84(dd, 2H).

PREPARATION EXAMPLE 3

[0187] Preparation of 2,6-difluoro-N-[1-methyl-l-(3-thenoyl)ethyl]benzamide (The after-mentioned Compound No. 6-5)

[0188] (1) 2.88 g of phenyltrimethylammonium tribromide was added to a mixed solution comprising 1.54 g of 2-(3-thenoyl)propane and 30 ml of tetrahydrofuran, followed by a reaction at room temperature for 15 hours. After completion of the reaction, the precipitate was separated by filtration and concentrated, and then purified by silica gel column chromatography (eluent: ethyl acetate/n-hexane=2/8-4/6) to obtain 0.87 of 2-bromo-2-(3-thenoyl)propane. The NMR spectrum data of this product were as follows.

[0189]

1
H-NMR δppm (Solvent: CDCl3/400 MHz) 2.06(s, 6H),7.27-7.31(m, 1H),7.74(dd, 1H),8.40(dd, 1H).

[0190] (2) 0.87 of 2-bromo-2-(3-thenoyl)propane was dissolved in 5 ml of dimethyl sulfoxide, then 0.44 g of sodium azide was added thereto and reacted at 70° C. for 1 hour. After completion of the reaction, the reaction mixture was allowed to cool and put into 200 ml of water, and then extracted with ethyl ether. The organic layer was washed with water, then dried over magnesium sulfate, followed by concentration to obtain 0.70 g of 2-azido-2-(3-thenoyl)propane. The NMR spectrum data of this product were as follows.

[0191]

1
H-NMR δppm (Solvent: CDCl3/400 MHz) 1.58(s, 6H),7.27-7.32(m, 1H),7.69(dd, 1H),8.45(dd, 1H).

[0192] (3) 4 ml of tetrahydrofuran and 0.08 ml of water were added to 0.68 g of 2-azido-2-(3-thenoyl)propane, then 1.10 g of triphenylphosphine was gradually added thereto with stirring at room temperature, and after completion of addition, a reaction was carried out for 18 hours. 15 ml of tetrahydrofuran was added to the reaction mixture, then 0.30 g of triethylamine was added, followed by cooling with ice, and a mixed solution of 0.46 g of 2,6-difluorobenzoyl chloride and 5 ml of tetrahydrofuran was dropwise added thereto. After completion of the dropwise addition, a reaction was carried out for 30 minutes under cooling with ice, and then a further reaction was carried out for 2.5 hours at room temperature. After completion of the reaction, the reaction mixture was put into 100 ml of water and extracted by ethyl acetate. The organic layer was dried over sodium sulfate, concentrated and purified by silica gel column chromatography (eluent: ethyl acetate/n-hexane=4/6) to obtain 0.60 g of the desired product having a melting point of from 139 to 142° C. The NMR spectrum data of this product were as follows.

[0193]

1
H-NMR δppm (Solvent: CDCl3/400 MHz) 1.81(s, 6H),6.92(t, 2H),7.12(br, 1H),7.29-7.38(m, 2H), 7.66(dd, 1H),8.24(dd, 1H).

PREPARATION EXAMPLE 4

[0194] Preparation of 2,6-difluoro-N-[(1,1-dimethyl-4′-methylsulfonyloxy)phenacyl]benzamide (Compond No. 1-25)

[0195] (1) 0.85 g of phenyltrimethylammonium tribromide was added to a mixture comprising 0.55 g of 4-methylsulfonyloxy isobutyrophenone and 10 ml of tetrahydrofuran, followed by a reaction at room temperature for 6 hours. After completion of the reaction, the reaction mixture was subjected to filtration, and the filtrate was concentrated under reduced pressure to obtain 0.68 g of oily α-bromo-4-methylsulfonyloxyisobutyrophenone. The NMR spectrum data of this product were as follows.

[0196]

1
H-NMR δppm (Solvent: CDCl3/400 MHz) 2.04(s, 6H),3.24(s, 3H),7.35(d, 2H),8.23(d, 2H)

[0197] (2) 0.28 g of sodium azide was added to a mixture comprising 0.68 g of a-bromo-4-methylsulfonyloxyisobutyrophenone and 4 ml of dimethyl sulfoxide, followed by a reaction at 50° C. for 3 hours. After completion of the reaction, the reaction mixture was put into water and then extracted with ethyl ether, followed by washing with water. The organic layer was dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure to obtain 0.55 g of α-azido-4-methylsulfonyloxyisobutyrophenone. The NMR spectrum data of this product were as follows.

[0198]

1
H-NMR δppm (Solvent: CDCl3/400 MHz) 1.61(s, 6H),3.20(s, 3H),7.39(d, 2H),8.21(d, 2H)

[0199] (3) 0.61 g of triphenylphosphine was added to a mixture comprising 0.55 g of α-azido-4-methylsulfonyloxyisobutyrophenone, 12.7 ml of tetrahydrofuran and 0.3 ml of water, followed by a reaction at room temperature for 16 hours. After completion of the reaction, the reaction mixture was concentrated under reduced pressure, and the residue was weakly acidified by adding water and then hydrochloric acid, and then washed with ethyl acetate. The aqueous layer was neutralized with an aqueous NaOH solution and extracted with methylene chloride, followed by drying over anhydrous sodium sulfate and concentration under reduced pressure to obtain 0.40 g of oily α-amino-4-methylsulfonyloxyisobutyrophenone.

[0200] (4) 0.19 g of triethylamine was added to a mixture comprising 0.40 g of α-amino-4-methylsulfonyloxyisobutyrophenone and 15 ml of tetrahydrofuran, and then 0.27 g of 2,6-difluorobenzoyl chloride was dropwise added thereto under cooling with ice. After completion of the dropwise addition, the mixture was reacted at room temperature for 2 hours. After completion of the reaction, the reaction mixture was washed with water and dried over anhydrous sodium sulfate, followed by concentration under reduced pressure. The obtained residue was purified by silica gel column chromatography (eluent: ethyl acetate/n-hexane=3/7) to obtain 0.50 g of the desired product having a melting point of from 158 to 162° C. The NMR spectrum data of this product were as follows.

[0201]

1
H-NMR δppm (Solvent: CDCl3/400 MHz) 1.78(s, 6H),3.15(s, 3H),6.89(s, 1H),6.91(t, 2H),7.32(d, 2H), 7.32-7.42(m, 1H),8.09(d, 2H).

PREPARATION EXAMPLE 5

[0202] Preparation of 2,6-difluoro-N-[(1,1-dimethyl-4′-hydroxy)phenacyl]benzamide (Compound No. 1-2)

[0203] At room temperature, a mixture comprising 0.3 g of sodium hydroxide and 15 ml of water was added to a mixture comprising 0.49 g of 2,6-difluoro-N-[(1,1-dimethyl-4′-methylsufonyloxy)phenacyl]benzamide and 30 ml of methanol, followed by a reaction under refluxing for 1 hour. After completion of the reaction, the reaction mixture was concentrated under reduced pressure, then the residue was diluted with water and weakly acidified with hydrochloric acid, and then the precipitated solid was collected by filtration, followed by drying to obtain 0.35 g of the desired product having a melting point of from 107 to 114° C. The NMR spectrum data of this product were as follows.

[0204]

1
H-NMR δppm (Solvent: CDCl3/400 MHz) 1.86(s, 6H),6.77(s, 1H),6.83(d, 2H),6.93(t, 2H),7.06(s, 1H), 7.30-7.40(m, 1H),8.02(d, 2H)

PREPARATION EXAMPLE 6

[0205] Preparation of 2,6-difluoro-N-[(1,1-dimethyl-4′-trifluoromethylsulfonyloxy)phenacyl]benzamide (Compound No. 1-26)

[0206] 0.102 g of trifluoromethanesulfonate anhydride was added to a mixture comprising 0.115 g of 2,6-difluoro-N-[(1,1-dimethyl-4′-hydroxy)phenacyl]benzamide, 7 ml of dichloroethane and 44 mg of triethylamine under cooling with ice, followed by a reaction at room temperature for 2 hours. After completion of the reaction, the reaction mixture was diluted with methylene chloride and washed with water, and then dried over anhydrous sodium sulfate, followed by concentration under reduced pressure. The obtained residue was purified by silica gel column chromatography (eluent: ethyl acetate/n-hexane=3/7) to obtain 0.14 g of the desired product having a melting point of from 117 to 123° C. The NMR spectrum data of this product were as follows.

[0207]

1
H-NMR δppm (Solvent: CDCl3/400 MHz) 1.78(s, 6H),6.60(s, 1H),6.91(t, 2H),7.31(d, 2H), 7.31-7.41(m, 1H),8.10(d, 2H).

PREPARATION EXAMPLE 7

[0208] Preparation of 2-methoxycarbonyl-N-[(4′-chloro-1,1-dimethyl)phenacyl]benzamide (The after-mentioned Compound No. 1-121)

[0209] A catalytic amount of concentrated sulfuric acid was added at room temperature to a mixed solution comprising 1.4 g of 2-hydroxycarbonyl-N-[(4′-chloro-1,1-dimethyl)phenacyl]benzamide and 100 ml of methanol, and the mixture was reacted under heating refluxing for 6 hours. After completion of the reaction, the methanol was distilled off and then 150 ml of water was added to the residue, followed by extraction with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was purified by silica gel column chromatography (eluent: ethyl acetate/n-hexane=2/8-4/6) to obtain 0.86 g of the desired product having a melting point of from 166 to 168° C. The NMR spectrum data of this product were as follows.

[0210]

1
H-NMR δppm (Solvent: CDCl3/400 MHz) 1.80(s, 6H),3.84(s, 3H),6.77(brs, 1H),7.18(dd, 1H), 7.41(dd, 2H),7.43-7.51(m, 2H),7.86(dd, 1H),7.98(dd, 2H).

PREPARATION EXAMPLE 8

[0211] Preparation of 2-aminocarbonyl-N-[(4′-chloro-1,1-dimethyl)phenacyl]benzamide (The after-mentioned Compound No. 1-122)

[0212] 10 ml of 28% aqueous ammonia was added at room temperature to a mixed solution comprising 0.58 g of 2-methoxycarbonyl-N-[(4′-chloro-l,1-dimethyl)phenacyl]benzamide and 15 ml of methanol, and the mixture was reacted overnight at room temperature. After completion of the reaction, the methanol was distilled off, and then 200 ml of water was added to the residue, followed by neutralization with 30% sulfuric acid, then by extraction with ethyl acetate and then by washing with a saturated sodium chloride aqueous solution. The organic layer was dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was purified by silica gel column chromatography (eluent: ethyl acetate/n-hexane=1/1-8/2) to obtain 0.39 g of the desired product having a melting point of from 205 to 206° C. The NMR spectrum data of this product were as follows.

[0213]

1
H-NMR δppm (Solvent: DMSO/400 MHz) 1.52(s, 6H),7.17-7.21(m, 1H),7.34(brs, 1H),7.41-7.49(m, 3H), 7.52(dd, 2H),7.68(brs, 1H),8.05(dd, 2H),9.09(s, 1H).

PREPARATION EXAMPLE 9

[0214] Preparation of 2-fluoro-N-[2-[(2,2,3,3,-tetrafluoro-5-methyl-1,4-benzodioxan-6-yl)carbonyl]-2-propyl]benzamide (The after-mentioned Compound No. 16-37)

[0215] (1) Under nitrogen atmosphere, 11.7 ml of n-butyllithium (1.57 M-n-hexane solution) was dropwise added at −20° C. to a mixture of 1.85 g of diisopropylamine and 50 ml of tetrahydrofuran, and then the mixture was stirred at the same temperature for 30 minutes. 5.0 g of 6-bromo-2,2,3,3,-tetrafluoro-1,4-benzodioxane was dropwise added thereto at a temperature of at most −50° C., followed by stirring at the same temperature for 30 minutes. Then, 5.5 ml of methyl iodide was dropwise added thereto at a temperature of at most −70° C., and then the temperature was raised to room temperature, followed by a reaction for 15 hours. After completion of the reaction, the reaction mixture was put into water and then weakly acidified by an addition of hydrochloric acid. Then, the mixture was extracted with ethyl ether, and the extract was washed with water and dried over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was purified by silica gel column chromatography (eluent: n-hexane) to obtain 3.40 g of oily 6-bromo-2,2,3,3,-tetrafluoro-5-methyl-1,4-benzodioxane. The NMR spectrum data of this product were as follows.

[0216]

1
H-NMR δppm (Solvent: CDC13/400 MHz) 2.39(s, 3H),6.89(d, 1H),6.91(t, 2H),7.35(d, 1H).

[0217] (2) Under nitrogen atmosphere, 7.8 ml of n-butyllithium (1.57 M-n-hexane solution) was dropwise added at −50° C. to a mixture comprising 3.36 g of 6-bromo-5 2,2,3,3,-tetrafluoro-5-methyl-1,4-benzodioxane and 40.6 ml of ethyl ether, and then the mixture was stirred at the same temperature for 30 minutes. 0.89 g of isobutylaldehyde was dropwise added thereto at a temperature of at most −70 ° C., and the temperature was raised to room temperature followed by a reaction for 15 hours. After completion of the reaction, the reaction mixture was put into water, and then weakly acidified by an addition of hydrochloric acid. Then the mixture was extracted with ether, and the extract was washed with water and dryied over magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was purified by silica gel column chromatography (eluent: ethyl acetate/n-hexane=1/9) to obtain 1.90 g of oily 1-(2,2,3,3,-tetrafluoro-5-methyl-1,4-benzodioxan-6-yl)-2-methylpropanol. The NMR spectrum data of this product were as follows.

[0218]

1
H-NMR δppm (Solvent: CDCl3/400 MHz) 0.87(d, 3H),1.00(d, 3H),1.94(m, 1H),2.29(s, 3H),4.65(d, 1H), 7.00(d, 1H),7.27(d, 1H).

[0219] (3) At room temperature, a mixture of 1.82 g of 1-(2,2,3,3-tetrafluoro-5-methyl-1,4-benzodioxan-6-yl)-2-methylpropanol and 7 ml of methylene chloride was added to a mixture of 2.0 g of pyridinium chlorochromate, 1.01 g of sodium acetate and 20 ml of methylene chloride, followed by a reaction at the same temperature for 2 hours. After completion of the reaction, the reaction mixture was filtrated by cerite, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (eluent: ethyl acetate/n-hexane=1/19) to obtain 1.70 g of oily 6-(2,2,3,3-tetrafluoro-5-methyl-1,4-benzodioxanyl) 2-propyl ketone. The NMR spectrum data of this product were as follows.

[0220]

1
H-NMR δppm (Solvent: CDCl3/400 MHz) 1.17(d, 6H),2.36(s, 3H),3.26(m, 1H),7.04(d, 1H),7.31(d, 1H).

[0221] (4) 2.15 g of phenyltrimethylammonium tribromide was added to a mixture comprising 1.67 g of 6-(2,2,3,3-tetrafluoro-5-methyl-1,4-benzodioxanyl) 2-propyl ketone and 20 ml of tetrahydrofuran, followed by a reaction at room temperature for 2 hours. After completion of the reaction, the reaction mixture was filtrated, and the filtrate was concentrated under reduced pressure to obtain 1.90 g of oily 6-(2,2,3,3-tetrafluoro-5-methyl-1,4-benzodioxanyl) 2-bromo-2-propyl ketone.

[0222] (5) 0.74 g of sodium azide was added to a mixture comprising 1.90 g of 6-(2,2,3,3-tetrafluoro-5-methyl-1,4-benzodioxanyl) 2-bromo-2-propyl ketone and 11 ml of dimethyl sulfoxide, followed by a reaction at 50° C. for 2 hours. After completion of the reaction, the reaction mixture was put into water and extracted with ethyl ether, and then washed with water. The organic layer was dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The obtained residue was purified by silica gel column chromatography (eluent: ethyl acetate/n-hexane=1/19) to obtain 0.90 g of the oily 6-(2,2,3,3-tetrafluoro-5-methyl-1,4-benzodioxanyl) 2-azido-2-propyl ketone. The NMR spectrum data of this product were as follows.

[0223]

1
H-NMR δppm (Solvent: CDCl3/400 MHz) 1.56(s, 6H),2.25(s, 3H),7.03(d, 1H),7.27(d, 1H).

[0224] (6) A mixture comprising 0.90 g of 6-(2,2,3,3-tetrafluoro-5-methyl-1,4-benzodioxanyl) 2-azido-2-propyl ketone, 20 ml of methanol and 50 mg of 5% palladium-carbon, was reacted at room temperature for 1 hour under hydrogen atmosphere. After completion of the reaction, the reaction mixture was filtrated by cerite, and then the filtrate was concentrated under reduced pressure, to obtain 0.70 g of oily 6-(2,2,3,3-tetrafluoro-5-methyl-1,4-benzodioxanyl) 2-amino-2-propyl ketone.

[0225] (7) 0.10 g of triethylamine was added to a mixture comprising 0.20 g of 6-(2,2,3,3-tetrafluoro-5-methyl-1,4-benzodioxanyl) 2-amino-2-propyl ketone and 7 ml of tetrahydrofuran. 0.11 g of 2-fluorobenzoyl chloride was dropwise added thereto under cooling with ice. After completion of the dropwise addition, a reaction was carried out at room temperature for 2 hours. After completion of the reaction, the reaction mixture was washed with water, and then dried over anhydrous sodium sulfate, followed by concentration under reduced pressure. The obtained residue was purified by silica gel column chromatography (eluent: ethyl acetate/n-hexane=3/7) to obtain 0.25 g of the desired product having a melting point of from 110 to 112° C. The NMR spectrum data of this product were as follows.

[0226]

1
H-NMR δppm (Solvent: CDCl3/400 MHz) 1.74(s, 6H),2.35(s, 3H),6.94(d, 1H),7.14(dq, 1H), 7.23(dt, 1H),7.30(s, 1H),7.42(d, 1H), 7.44-7.50(m, 1H),7.92(dt, 1H)

PREPARATION EXAMPLE 10

[0227] Preparation of 2,6-difluoro-N-[(3′-methoxycarbonyl-1,1-dimethyl)phenacyl]benzamide (The after-mentioned Compound No. 1-221)

[0228] (1) A mixture comprising 2.48 g of m-iodobenzoic acid and 40 ml of tetrahydrofuran was cooled to −70° C., then 13.8 ml of n-butyllithium (1.6 M-n-hexane solution) was dropwise added over a period of 10 minutes, followed by stirring at the same temperature for 30 minutes. Then, a mixture comprising 1.5 g of N-isobutyrylpropyleneimine and 5 ml of tetrahydrofuran was added thereto at −70° C., and then the temperature was raised to room temperature, and a reaction was carried out overnight.

[0229] After completion of the reaction, the reaction mixture was added to 100 ml of water and stirred, and then hexane was added thereto, followed by liquid separation. The aqueous layer was acidified by concentrated hydrochloric acid and then extracted with ethyl acetate. The extract was dried over anhydrous sodium sulfate, followed by concentration under reduced pressure to obtain a crude product of m-isobutyrylbenzoic acid.

[0230] (2) 100 ml of toluene and 5 g of thionyl chloride were added to the crude product of m-isobutyrylbenzoic acid obtained in the above step (1), and the mixture was reacted under refluxing for 1 hour. After completion of the reaction, excess thionyl chloride was distilled off to obtain a toluene solution of crude m-isobutyrylbenzoic acid chloride.

[0231] (3) The toluene solution of crude m-isobutyrylbenzoic acid chloride obtained in the above step (2) was dropwise added under cooing with ice to a mixture comprising 5 g of triethylamine and 100 ml of methanol, and the mixture was heated to room temperature and reacted for 1 hour. After completion of the reaction, methanol and toluene were distilled off under reduced pressure. Then, 200 ml of water was added thereto, followed by extraction with ethyl acetate, and then the extract was dried over anhydrous sodium sulfate, followed by concentration under reduced pressure to obtain 1.5 g of a crude product of methyl m-isobutyrylbenzoate.

[0232] (4) 0.8 g of phenyltrimethylammonium tribromide was added to a mixture comprising 1.5 g of the crude product of methyl m-isobutyrylbenzoate obtained in the above step (3) and 20 ml of tetrahydrofuran, and followed by a reaction at room temperature overnight. After completion of the reaction, the precipitated crystal was separated by filtration, then tetrahydrofuran was distilled off. The residue was dissolved in ethyl acetate, then washed with a saturated sodium chloride aqueous solution, followed by drying over anhydrous sodium sulfate. Then, concentration under reduced pressure was carried out, and then, rough purification was carried out by silica gel column chromatography to obtain 0.27 g of crude 3′-methoxycarbonyl-2-bromo-2-methylpropiophenone. The NMR spectrum data of this product were as follows.

[0233]

1
H-NMR δppm (Solvent: CDCl3/400 MHz) 2.05(s, 6H),3.98(s, 3H),7.52-7.57(m, 1H),8.19-8.25(m, 1H), 8.31-8.34(m, 1H),8.78(t, 1H).

[0234] (5) 17 mg of a crude product containing the desired product was obtained by employing 0.27 g of the crude 3′-methoxycarbonyl-2-bromo-2-methylpropiophenone obtained in the above step (4), in accordance with the steps (5) to (7) in Preparation Example 9. The NMR spectrum data of this product were as follows.

[0235]

1
H-NMR δppm (Solvent: CDCl3/400 MHz) 1.81(s, 6H),3.93(s, 3H),6.85-6.91(m, 3H),7.27-7.34(m, 1H), 7.47-7.53(m, 1H),8.16-8.20(m, 2H),8.65(t, 1H).

PREPARATION EXAMPLE 11

[0236] Preparation of 2,6-difluoro-N-[2-(5-trifluoromethyl-2-pyridylcarbonyl)-2-propyl]benzamide (The after-mentioned Compound No. 8-43)

[0237] 10 mg of a crude product containing the desired product was obtained by employing 2.26 g of 2-bromo-5-trifluoromethylpyridine, in accordance with the steps (1), (4) and (5) in Preparation Example 10. The NMR spectrum data of this product were as follows.

[0238]

1
H-NMR δppm (Solvent: CDCl3/400 MHz) 1.89(s, 6H),6.71(br, 1H),6.83-6.88(m, 2H),7.26-7.36(m, 1H), 10 8.04-8.11(m, 1H),8.76(s, 1H).

[0239] Now, typical examples of the compound of the present invention of the above formula (I) will be given in Tables 1 to 53. These compounds can be prepared in accordance with the above Preparation Examples or by the above-described various processes for the production of the compounds of the present invention.

[0240] In the table, Me indicates a methyl group, Et an ethyl group, Bu a butyl group, and Ph a phenyl group. Further, Ph(2-F) indicates that a fluorine atom is substituted at the 2-position. The same applies to other expressions.

1TABLE 1

PhysicalCompoundpropertiesNo.R1R2R3XB(mp ° C.)1-1MeMeH4-OHPh(2-F)1-2MeMeH4-OHPh(2,6-F2)107-1141-3MeMeH4-OHPh(2-Cl)1-4MeMeH4-OHPh(2-CF3)1-5MeMeH4-OCOMePh(2-F)1-6MeMeH4-OCOMePh(2,6-F2)1-7MeMeH4-OCOCF3Ph(2-F)1-8MeMeH4-OCOCF3Ph(2,6-F2)1-9MeMeH4-OCO2MePh(2-F)1-10MeMeH4-OCO2MePh(2,6-F2)46-511-11MeMeH4-OCONMe2Ph(2-F)1-12MeMeH4-OCONMe2Ph(2,6-F2)136-1421-13MeMeH4-OCOSPhPh(2-F)1-14MeMeH4-OCOSMePh(2,6-F2)82-881-15MeMeH4-OCOSMePh(2-F)1-16MeMeH4-OCSOMePh(2,6-F2)1-17MeMeH4-OCS2MePh(2-F)1-18MeMeH4-OCS2MePh(2,6-F2)1-19MeMeH4-OCSNMe2Ph(2-F)1-20MeMeH4-OCSNMe2Ph(2,6-F2)1-21MeMeH4-OCS2MePh(2-F)1-22MeMeNa4-OCS2MePh(2,6-F2)1-23MeMeH4-OSCCl3Ph(2-F)1-24MeMeH4-OSOMePh(2,6-F2)1-25MeMeH4-OSO2MePh(2,6-F2)158-1621-26MeMeH4-OSO2CF3Ph(2,6-F2)117-1231-27MeMeH4-OSO2PhPh(2-F)1-28MeMeH4-OSO2PhPh(2,6-F2)1-29MeMeH4-OSNMe2Ph(2,6-F2)1-30MeMeH4-OSO2NMe2Ph(2-F)1-31MeMeH4-OSO2NMe2Ph(2,6-F2)Oil1-32MeMeH4-NH2Ph(2-F)1-33MeMeH4-NH2Ph(2,6-F2)170-1801-34MeMeH4-NH2.HClPh(2,6-F2)142-1551-35MeMeH4-NHCOMePh(2-F)1-36MeMeH4-Ph(2,6-F2)275-281NHCOBu(t)1-37MeMeH4-NHCOCF3Ph(2-F)1-38MeMeH4-NHCOCF3Ph(2,6-F2)1-39MeMeH4-NHCO2MePh(2-F)1-40MeMeH4-NHCO2MePh(2,6-F2)1-41MeMeH4-Ph(2-F)N(Me)CO2Me1-42MeMeH4-NHCONMe2Ph(2,6-F2)1-43MeMeH4-NHCOSMePh(2-F)1-44MeMeH4-NHCOSMePh(2,6-F2)1-45MeMeH4-NHCSOMePh(2-F)1-46MeMeH4-NHCSOMePh(2,6-F2)1-47MeMeH4-NHCS2MePh(2-F)1-48MeMeH4-NHCS2MePh(2,6-F2)1-49MeMeH4-NHCSNMe2Ph(2-F)1-50MeMeH4-NHCSNMe2Ph(2,6-F2)1-51MeMeH4-NHCS2PhPh(2-F)1-52MeMeH4-NHCS2PhPh(2,6-F2)1-53MeMeH4-NHSCCl3Ph(2-F)1-54MeMeH4-NHSOMePh(2,6-F2)1-55MeMeH4-NHSO2MePh(2-F)1-56MeMeH4-NHSO2MePh(2,6-F2)195-2331-57MeMeH4-NHSO2PhPh(2-F)1-58MeMeH4-NHCOPhPh(2,6-F2)270-2831-59MeMeSCCl34-FPh(2-F)1-60MeMeSCCl34-ClPh(2,6-F2)1-61MeMeSPh4-BrPh(2-F)1-62MeMeSPh4-FPh(2,6-F2)1-63MeMeSOPh4-ClPh(2,6-F2)1-64MeMeSO2Me4-BrPh(2-F)1-65MeMeSO2Me4-FPh(2,6-F2)1-66MeMeSO2Ph4-ClPh(2-F)1-67MeMeSO2Ph4-BrPh(2,6-F2)1-68MeMeSO2NMe24-FPh(2-F)1-69MeMeSO2NMe24-ClPh(2,6-F2)1-70MeMeSO2CF34-BrPh(2-F)1-71MeMeSO2CF34-FPh(2,6-F2)1-72MeMeH4-CO2HPh(2,6-F2)215-2181-73MeMeH4-CO2MePh(2,6-F2)58-601-74MeMeH4-CO2EtPh(2,6-F2)1-75MeMeH4-CONH2Ph(2,6-F2)>2501-76MeMeH4-CONHMePh(2,6-F2)244-2591-77MeMeH4-CONMe2Ph(2,6-F2)158-1601-78MeMeH4-ClPh(2-CO2H)212-2141-79MeMeH4-ClPh(2-(2-thienyl))1-80MeMeH4-ClPh(2-(3-thienyl))170-1731-81MeMeH4-ClPh(2-(2-pyridyl))1-82MeMeH4-ClPh(2-(3-pyridyl))1-83MeMeH4-ClPh(2-(4-pyridyl))1-84MeMeH4-BrPh(2-CO2H)197-1991-85MeMeH4-BrPh(2-(2-thienyl))1-86MeMeH4-BrPh(2-(3-thienyl))1-87MeMeH4-BrPh(2-(2-pyridyl))1-88MeMeH4-BrPh(2-(3-pyridyl))1-89MeMeH4-BrPh(2-(4-pyridyl))1-90MeMeH4-(2-pyridyl)Ph(2,6-F2)1-91MeMeH4-(3-pyridyl)Ph(2,6-F2)1-92MeMeH4-(4-pyridyl)Ph(2,6-F2)1-93MeMeH4-(2-thienyl)Ph(2-F)110-1121-94MeMeH4-(3-thienyl)Ph(2-F)143-1451-95MeMeH4-(2-thienyl)Ph(2,6-F2)1-96MeMeH4-(3-thienyl)Ph(2,6-F2)1-97MeMeH4-ClPh(2-CO2Me)1-98MeMeHHPh(2-CO2Me)1-99MeCO2EtHHPh(2-F)122-1231-100MeCO2EtHHPh(2.6-F2)117-1191-101MeCNHHPh(2-F)Oil1-102MeCNHHPh(2,6-F2)45-481-103MeMeH4-Br1-naphthyl1-104MeMeH4-Br2-naphthyl1-105MeMeH4-Br2-thienyl235-2401-106MeMeH4-Br3-thienyl245-2471-107MeMeH4-Br2-pyrazinyl122-1251-108MeMeH4-Br2-quinolyl1-109MeMeH4-Br3-quinolyl192-1951-110MeMeH4-BrIndol-2-yl1-111MeMeH4-BrIndol-3-yl1-112MeMeH4-Br3-furyl1-113MeMeH4-Br2,5-dimethyl-3-183-185furyl1-114MeMeH4-Br2-furyl1-115MeMeH4-Br5-nitro-2-furyl132-1341-116MeMeH4-BrBenzofuran-2-yl164-1661-117MeMeH4-Br2,3-145-147dihydrobenzofuran-2-yl1-118MeMeH4-Br1,4-benzodioxane-45-472-yl1-119MeMeH4-BrN-methylindol-2-yl50-581-120MeMeH4-ClPh(2-CO2H)212-2141-121MeMeH4-ClPh(2-CO2Me)166-1681-122MeMeH4-ClPh(2-CONH2)205-2061-123MeMeH4-OSO2MePh(2-F)130-1331-124MeMeH4-OSO2MePh(2-Cl)1-125MeMeH4-OSO2CF3Ph(2-F)72-751-126MeMeH4-OSO2CF3Ph(2-Cl)1-127MeMeH4-SCH2CF3Ph(2,6-F2)110-1121-128MeMeH4-SCH2CF3Ph(2-F)Oil1-129MeMeH4-SCH2CF3Ph(2-Cl)1-130MeMeH4-SCHF2Ph(2,6-F2)108-1101-131MeMeH4-SCHF2Ph(2-F)77-791-132MeMeH4-SCHF2Ph(2-Cl)1-133MeMeH4-SO2CH2CF3Ph(2,6-F2)175-1781-134MeMeH4-SO2CH2CF3Ph(2-F)135-1391-135MeMeH4-SO2CH2CF3Ph(2-Cl)1-136MeMeH4-SO2CHF2Ph(2,6-F2)140-1441-137MeMeH4-SO2CHF2Ph(2-F)85-881-138MeMeH4-SO2CHF2Ph(2-C1)1-139MeMeH2-Me-4-OSO2MePh(2,6-F2)112-1151-140MeMeH2-Me-4-OSO2CF3Ph(2,6-F2)108-1101-141MeMeH2-Me-4-OCF2CHFOCF3Ph(2-F)1-142MeMeH2-Me-4-OCF2CHFOCF3Ph(2,6-F2)1-143MeMeH2-Me-4-OCF2CHFOCF3Ph(2-Cl)1-144MeMeH2-Me-4-OCF2CHFOCF3Ph(2-Me)1-145MeMeH2-Me-4-OCF2CHFOCF3Ph(2-CF3)1-146MeMeH2-Me-4-OCF2CHFOCF3Ph(2-F-6-Cl)1-147MeMeH2-Cl-4-OCF2CHFOCF3Ph(2-F)1-148MeMeH2-Cl-4-OCF2CHFOCF3Ph(2,6-F2)1-149MeMeH2-Cl-4-OCF2CHFOCF3Ph(2-Cl)1-150MeMeH2-Cl-4-OCF2CHFOCF3Ph(2-Me)1-151MeMeH2-Cl-4-OCF2CHFOCF3Ph(2-CF3)1-152MeMeH2-Cl-4-OCF2CHFOCF3Ph(2-F-6-Cl)1-153MeMeH2,3-Me2-4-OCF2CHFOCF3Ph(2-F)1-154MeMeH2,3-Me2-4-OCF2CHFOCF3Ph(2,6-F2)1-155MeMeH2,3-Me2-4-OCF2CHFOCF3Ph(2-Cl)1-156MeMeH2,3-Me2-4-OCF2CHFOCF3Ph(2-Me)1-157MeMeH2,3-Me2-4-OCF2CHFOCF3Ph(2-CF3)1-158MeMeH2,3-Me2-4-OCF2CHFOCF3Ph(2-F-6-Cl)1-159MeMeH2-Me-3-OMe-4-OCF2CHFOCF3Ph(2-F)1-160MeMeH2-Me-3-OMe-4-OCF2CHFOCF3Ph(2,6-F2)1-161MeMeH2-Me-3-OMe-4-OCF2CHFOCF3Ph(2-Cl)1-162MeMeH2-Me-3-OMe-4-OCF2CHFCCF3Ph(2-Me)1-163MeMeH2-Me-3-OMe-4-OCF2CHFOCF3Ph(2-CF3)1-164MeMeH2-Me-3-OMe-4-OCF2CHFOCF3Ph(2-F-6-Cl)1-165MeMeH2-Me-3-OCHF2-4-OCF2CHFOCF3Ph(2-F)1-166MeMeH2-Me-3-OCHF2-4-OCF2CHFOCF3Ph(2,6-F2)1-167MeMeH2-Me-3-OCHF2-4-OCF2CHFOCF3Ph(2-Cl)1-168MeMeH2-Me-3-OCHF2-4-OCF2CHFOCF3Ph(2-Me)1-169MeMeH2-Me-3-OCHF2-4-OCF2CHFOCF3Ph(2-CF3)1-170MeMeH2-Me-3-OCHF2-4-OCF2CHFOCF3Ph(2-F-6-Cl)1-171MeMeH4-BrPh(2-253-254CONHCH2CH(Me)2)1-172MeMeH4-BrPh(2-CONHMe)252-2551-173MeMeH4-BrPh(2-CONH2)193-1961-174MeMeH4-BrPh(2-OCOMe)163-1661-175MeMeH4-BrPh(2-CO2Me)151-1541-176MeMeH4-ClPh(2-CO2Me)166-1681-177MeMeH4-ClPh(2-CONH2)205-2061-178MeMeH2-CO2HPh(2-F)1-179MeMeH2-CO2HPh(2,6-F2)1-180MeMeH2-CO2HPh(2-Cl)1-181MeMeH2-CO2HPh(2-Me)1-182MeMeH2-CO2HPh(2-CF3)1-183MeMeH2-CO2HPh(2-F-6-Cl)1-184MeMeH2-CO2MePh(2-F)1-185MeMeH2-CO2MePh(2,6-F2)1-186MeMeH2-CO2MePh(2-Cl)1-187MeMeH2-CO2MePh(2-Me)1-188MeMeH2-CO2MePh(2-CF3)1-189MeMeH2-CO2MePh(2-F-6-Cl)1-190MeMeH2-CO2EtPh(2-F)1-191MeMeH2-CO2EtPh(2,6-F2)1-192MeMeH2-CO2EtPh(2-C1)1-193MeMeH2-CO2EtPh(2-Me)1-194MeMeH2-CO2EtPh(2-CF3)1-195MeMeH2-CO2EtPh(2-F-6-Cl)1-196MeMeH2-CONH2Ph(2-F)1-197MeMeH2-CONH2Ph(2,6-F2)1-198MeMeH2-CONH2Ph(2-Cl)1-199MeMeH2-CONH2Ph(2-Me)1-200MeMeH2-CONH2Ph(2-CF3)1-201MeMeH2-CONH2Ph(2-F-6-Cl)1-202MeMeH2-CONHMePh(2-F)1-203MeMeH2-CONHMePh(2,6-F2)1-204MeMeH2-CONHMePh(2-Cl)1-205MeMeH2-CONHMePh(2-Me)1-206MeMeH2-CONHMePh(2-CF3)1-207MeMeH2-CONHMePh(2-F-6-Cl)1-208MeMeH2-CONMe2Ph(2-F)1-209MeMeH2-CONMe2Ph(2,6-F2)1-210MeMeH2-CONMe2Ph(2-Cl)1-211MeMeH2-CONMe2Ph(2-Me)1-212MeMeH2-CONMe2Ph(2-CF3)1-213MeMeH2-CONMe2Ph(2-F-6-Cl)1-214MeMeH3-CO2HPh(2-F)1-215MeMeH3-CO2HPh(2,6-F2)1-216MeMeH3-CO2HPh(2-Cl)1-217MeMeH3-CO2HPh(2-Me)1-218MeMeH3-CO2HPh(2-CF3)1-219MeMeH3-CO2HPh(2-F-6-Cl)1-220MeMeH3-CO2MePh(2-F)1-221MeMeH3-CO2MePh(2,6-F2)Oil1-222MeMeH3-CO2MePh(2-Cl)1-223MeMeH3-CO2MePh(2-Me)1-224MeMeH3-CO2MePh(2-CF3)1-225MeMeH3-CO2MePh(2-F-6-Cl)1-226MeMeH3-CO2EtPh(2-F)1-227MeMeH3-CO2EtPh(2,6-F2)1-228MeMeH3-CO2EtPh(2-Cl)1-229MeMeH3-CO2EtPh(2-Me)1-230MeMeH3-CO2EtPh(2-CF3)1-231MeMeH3-CO2EtPh(2-F-6-Cl)1-232MeMeH3-CONH2Ph(2-F)1-233MeMeH3-CONH2Ph(2,6-F2)1-234MeMeH3-CONH2Ph(2-Cl)1-235MeMeH3-CONH2Ph(2-Me)1-236MeMeH3-CONH2Ph(2-CF3)1-237MeMeH3-CONH2Ph(2-F-6-Cl)1-238MeMeH3-CONHMePh(2-F)1-239MeMeH3-CONHMePh(2,6-F2)1-240MeMeH3-CONHMePh(2-Cl)1-241MeMeH3-CONHMePh(2-Me)1-242MeMeH3-CONHMePh(2-CF3)1-243MeMeH3-CONHMePh(2-F-6-Cl)1-244MeMeH3-CONMe2Ph(2-F)1-245MeMeH3-CONMe2Ph(2,6-F2)1-246MeMeH3-CONMe2Ph(2-Cl)1-247MeMeH3-CONMe2Ph(2-Me)1-248MeMeH3-CONMe2Ph(2-CF3)1-249MeMeH3-CONMe2Ph(2-F-6-Cl)

[0241]

2

TABLE 2

Physical

Compound

properties

No.
R1
R2
R3
X
B
(mp ° C.)

2-1
Me
Me
H
4-Cl
Ph(2-F)

2-2
Me
Et
H
4-Cl
Ph(2-F)

2-3
—(CH2)2—
H
4-Cl
Ph(2-F)

2-4
Me
Me
H
4-Cl
Ph(2-6-F2)
144-153

2-5
Me
Me
H
4-Cl
Ph(2-Cl)

2-6
Me
Et
H
4-Cl
Ph(2-C1)

2-7
Me
Me
COMe
4-Cl
Ph(2-Cl)

2-8
—(CH2)2—
H
4-Cl
Ph(2-Cl)

2-9
—(CH2)4—
H
4-Cl
Ph(2-Cl)

2-10
Me
Me
H
4-Cl
Ph(2-CF3)

2-11
Me
Me
H
4-Br
Ph(2-F)

2-12
Me
Me
H
4-Br
Ph(2,6-F2)

2-13
Me
Me
H
4-Br
Ph(2-Cl)

2-14
Me
Me
H
4-Br
Ph(2-CF3)

2-15
Me
Me
H
4-F
Ph(2-F)

2-16
Me
Me
H
4-F
Ph(2,6-F2)

2-17
Me
Me
H
4-F
Ph(2-Cl)

2-18
Me
Me
H
4-F
Ph(2-CF3)

2-19
Me
Me
H
4-CF3
Ph(2-F)

2-20
Me
Me
H
4-CF3
Ph(2,6-F2)

2-21
Me
Me
H
4-CF3
Ph(2-Cl)

2-22
Me
Me
H
4-CF3
Ph(2-CF3)

2-23
Me
Me
H
3,4-Cl2
Ph(2-F)

2-24
Me
Me
H
3,4-Cl2
Ph(2,6-F2)

2-25
—(CH2)2—
H
3,4-Cl2
Ph(2-Cl)

2-26
—(CH2)5—
H
3,4-Cl2
Ph(2-CF3)

2-27
Me
Me
Me
2,4-Cl2
Ph(2-F)

2-28
Me
Me
H
2,4-Cl2
Ph(2-F)

2-29
Me
Me
H
2,4-Cl2
Ph(2,6-F2)

2-30
Me
Me
H
2,4-Cl2
Ph(2-Cl)

2-31
Me
Me
H
2,4-Cl2
Ph(2-CF3)

2-32
Me
Me
H
2,4-F2
Ph(2-F)

2-33
Me
Me
H
2,4-F2
Ph(2,6-F2)

2-34
Me
Me
H
4-OCF3
Ph(2-F)

2-35
Me
Me
H
4-OCF3
Ph(2,6-F2)

2-36
Me
Me
H
4-OCF3
Ph(2-Cl)

2-37
Me
Me
H
4-OCF3
Ph(2-Me)

2-38
Me
Me
H
4-OCF3
Ph(2-CF3)

2-39
Me
Me
H
4-OCF3
Ph(2-F-6-Cl)

2-40
Me
Me
H
4-OCHF2
Ph(2-F)

2-41
Me
Me
H
4-OCHF2
Ph(2,6-F2)

2-42
Me
Me
H
4-OCHF2
Ph(2-Cl)

2-43
Me
Me
H
4-OCHF2
Ph(2-Me)

2-44
Me
Me
H
4-OCHF2
Ph(2-CF3)

2-45
Me
Me
H
4-OCHF2
Ph(2-F-6-Cl)

2-46
Me
Me
H
4-OCH2CF3
Ph(2-F)

2-47
Me
Me
H
4-OCH2CF3
Ph(2,6-F2)

2-48
Me
Me
H
4-OCH2CF3
Ph(2-Cl)

2-49
Me
Me
H
4-OCH2CF3
Ph(2-Me)

2-50
Me
Me
H
4-OCH2CF3
Ph(2-CF3)

2-51
Me
Me
H
4-OCH2CF3
Ph(2-F-6-Cl)

2-52
Me
Me
H
2-Me-4-Cl
Ph(2-F)

2-53
Me
Me
H
2-Me-4-Cl
Ph(2,6-F2)

2-54
Me
Me
H
2-Me-4-Cl
Ph(2-Cl)

2-55
Me
Me
H
2-Me-4-Cl
Ph(2-Me)

2-56
Me
Me
H
2-Me-4-Cl
Ph(2-CF3)

2-57
Me
Me
H
2-Me-4-Cl
Ph(2-F-6-Cl)

2-58
Me
Me
H
2-Me-4-Br
Ph(2-F)

2-59
Me
Me
H
2-Me-4-Br
Ph(2,6-F2)

2-60
Me
Me
H
2-Me-4-Br
Ph(2-Cl)

2-61
Me
Me
H
2-Me-4-Br
Ph(2-Me)

2-62
Me
Me
H
2-Me-4-Br
Ph(2-CF3)

2-63
Me
Me
H
2-Me-4-Br
Ph(2-F-6-Cl)

2-64
Me
Me
H
2-Me-4-OCF3
Ph(2-F)

2-65
Me
Me
H
2-Me-4-OCF3
Ph(2,6-F2)

2-66
Me
Me
H
2-Me-4-OCF3
Ph(2-Cl)

2-67
Me
Me
H
2-Me-4-OCF3
Ph(2-Me)

2-68
Me
Me
H
2-Me-4-OCF3
Ph(2-CF3)

2-69
Me
Me
H
2-Me-4-OCF3
Ph(2-F-6-Cl)

2-70
Me
Me
H
2-Me-4-OCHF2
Ph(2-F)

2-71
Me
Me
H
2-Me-4-OCHF2
Ph(2-6-F2)

2-72
Me
Me
H
2-Me-4-OCHF2
Ph(2-Cl)

2-73
Me
Me
H
2-Me-4-OCHF2
Ph(2-Me)

2-74
Me
Me
H
2-Me-4-OCHF2
Ph(2-CF3)

2-75
Me
Me
H
2-Me-4-OCHF2
Ph(2-F-6-Cl)

2-76
Me
Me
H
2-Me-4-OCH2CF3
Ph(2-F)

2-77
Me
Me
H
2-Me-4-OCH2CF3
Ph(2,6-F2)

2-78
Me
Me
H
2-Me-4-OCH2CF3
Ph(2-Cl)

2-79
Me
Me
H
2-Me-4-OCH2CF3
Ph(2-Me)

2-80
Me
Me
H
2-Me-4-OCH2CF3
Ph(2-CF3)

2-81
Me
Me
H
2-Me-4-OCH2CF3
Ph(2-F-6-Cl)

2-82
Me
Me
H
2-Me-4-CF3
Ph(2-F)

2-83
Me
Me
H
2-Me-4-CF3
Ph(2,6-F2)

2-84
Me
Me
H
2-Me-4-CF3
Ph (2-Cl)

2-85
Me
Me
H
2-Me-4-CF3
Ph(2-Me)

2-86
Me
Me
H
2-Me-4-CF3
Ph(2-CF3)

2-87
Me
Me
H
2-Me-4-CF3
Ph(2-F-6-Cl)

2-88
Me
Me
H
2-Cl-4-Br
Ph(2-F)

2-89
Me
Me
H
2-Cl-4-Br
Ph(2,6-F2)

2-90
Me
Me
H
2-Cl-4-Br
Ph(2-Cl)

2-91
Me
Me
H
2-Cl-4-Br
Ph(2-Me)

2-92
Me
Me
H
2-Cl-4-Br
Ph(2-CF3)

2-93
Me
Me
H
2-Cl-4-Br
Ph(2-F-6-Cl)

2-94
Me
Me
H
2-Cl-4-OCF3
Ph(2-F)

2-95
Me
Me
H
2-Cl-4-OCF3
Ph(2,6-F2)

2-96
Me
Me
H
2-Cl-4-OCF3
Ph(2-Cl)

2-97
Me
Me
H
2-Cl-4-OCF3
Ph(2-Me)

2-98
Me
Me
H
2-Cl-4-OCF3
Ph(2-CF3)

2-99
Me
Me
H
2-Cl-4-OCF3
Ph(2-F-6-Cl)

2-100
Me
Me
H
2-Cl-4-OCHF2
Ph(2-F)

2-101
Me
Me
H
2-Cl-4-OCHF2
Ph(2,6-F2)

2-102
Me
Me
H
2-Cl-4-OCHF2
Ph(2-Cl)

2-103
Me
Me
H
2-Cl-4-OCHF2
Ph(2-Me)

2-104
Me
Me
H
2-Cl-4-OCHF2
Ph(2-CF3)

2-105
Me
Me
H
2-Cl-4-OCHF2
Ph(2-F-6-Cl)

2-106
Me
Me
H
2-Cl-4-OCH2CF3
Ph(2-F)

2-107
Me
Me
H
2-Cl-4-OCH2CF3
Ph(2,6-F2)

2-108
Me
Me
H
2-Cl-4-OCH2CF3
Ph(2-Cl)

2-109
Me
Me
H
2-Cl-4-OCH2CF3
Ph(2-Me)

2-110
Me
Me
H
2-Cl-4-OCH2CF3
Ph(2-CF3)

2-111
Me
Me
H
2-Cl-4-OCH2CF3
Ph(2-F-6-Cl)

[0242]

3

TABLE 3

Physical

Compound

properties

No.
R1
R2
R3
X
B
(mp ° C.)

3-1
Me
Me
H
H
Ph

3-2
Me
Me
H
H
Ph(2-F)
<30 yellow

resin

3-3
Me
Me
H
H
Ph(2-Cl)

3-4
Me
Me
H
H
Ph(2-OMe)

3-5
Me
Me
H
H
Ph(2,6-F2)

3-6
Me
Me
H
H
Ph(2,6-Cl2)

3-7
Me
Me
H
H
Ph(2,6-OMe2)

3-8
Me
Me
H
6-Cl
Ph

3-9
Me
Me
H
6-Cl
Ph(2-F)

3-10
Me
Me
H
6-Cl
Ph(2-Cl)

3-11
Me
Me
H
6-Cl
Ph(2,6-F2)

3-12
Me
Me
H
6-Cl
Ph(2,6-Cl2)

3-13
Me
Me
H
6-Br
Ph

3-14
Me
Me
H
6-Br
Ph(2-F)

3-15
Me
Me
H
6-Br
Ph(2-Cl)

3-16
Me
Me
H
6-Br
Ph(2,6-F2)

3-17
Me
Me
H
6-Br
Ph(2,6-Cl2)

3-18
Me
Me
H
6-CF3
Ph(2,6-F2)

3-19
Me
Me
H
6-CN
Ph(2,6-F2)

3-20
Me
CN
H
H
Ph(2,6-F2)

3-21
Me
CO2Et
H
H
Ph(2,6-F2)

3-22
Me
CN
H
6-Cl
Ph(2,6-F2)

3-23
Me
CO2Et
H
6-Cl
Ph(2,6-F2)

3-24
Me
Et
H
H
Ph(2,6-F2)

3-25
Me
Me
COMe
H
Ph(2,6-F2)

3-26
Me
Me
CH2OMe
H
Ph(2,6-F2)

3-27
Me
Me
H
H
1-naphthyl

3-28
Me
Me
H
H
2-naphthyl

3-29
Me
Me
H
H
2-thienyl

3-30
Me
Me
H
H
3-thienyl

3-31
Me
Me
H
H
2-pyrazinyl

3-32
Me
Me
H
H
2-pyridyl

3-33
Me
Me
H
H
3-pyridyl

3-34
Me
Me
H
H
4-

trifluoromethyl-

3-pyridyl

3-35
Me
Me
H
H
4-pyridyl

3-36
Me
Me
H
H
2-furyl

3-37
Me
Me
H
H
3-furyl

3-38
Me
Me
H
2-Cl
Ph(2-F)

3-39
Me
Me
H
2-Cl
Ph(2,6-F2)

3-40
Me
Me
H
2-Cl
Ph(2-Cl)

3-41
Me
Me
H
2-Cl
Ph(2-Me)

3-42
Me
Me
H
2-Cl
Ph(2-CF3)

3-43
Me
Me
H
2-Cl
Ph(2-F-6-Cl)

3-44
Me
Me
H
2-Br
Ph(2-F)

3-45
Me
Me
H
2-Br
Ph(2,6-F2)

3-46
Me
Me
H
2-Br
Ph(2-Cl)

3-47
Me
Me
H
2-Br
Ph(2-Me)

3-48
Me
Me
H
2-Br
Ph(2-CF3)

3-49
Me
Me
H
2-Br
Ph(2-F-6-Cl)

3-50
Me
Me
H
2-CF3
Ph(2-F)

3-51
Me
Me
H
2-CF3
Ph(2,6-F2)

3-52
Me
Me
H
2-CF3
Ph(2-Cl)

3-53
Me
Me
H
2-CF3
Ph(2-Me)

3-54
Me
Me
H
2-CF3
Ph(2-CF3)

3-55
Me
Me
H
2-CF3
Ph(2-F-6-Cl)

3-56
Me
Me
H
2-OCF3
Ph(2-F)

3-57
Me
Me
H
2-OCF3
Ph(2,6-F2)

3-58
Me
Me
H
2-OCF3
Ph(2-Cl)

3-59
Me
Me
H
2-OCF3
Ph(2-Me)

3-60
Me
Me
H
2-OCF3
Ph(2-CF3)

3-61
Me
Me
H
2-OCF3
Ph(2-F-6-Cl)

3-62
Me
Me
H
2-OCHF2
Ph(2-F)

3-63
Me
Me
H
2-OCHF2
Ph(2,6-F2)

3-64
Me
Me
H
2-OCHF2
Ph(2-Cl)

3-65
Me
Me
H
2-OCHF2
Ph(2-Me)

3-66
Me
Me
H
2-OCHF2
Ph(2-CF3)

3-67
Me
Me
H
2-OCHF2
Ph(2-F-6-Cl)

3-68
Me
Me
H
2-OCH2CF3
Ph(2-F)

3-69
Me
Me
H
2-OCH2CF3
Ph(2,6-F2)

3-70
Me
Me
H
2-OCH2CF3
Ph(2-Cl)

3-71
Me
Me
H
2-OCH2CF3
Ph(2-Me)

3-72
Me
Me
H
2-OCH2CF3
Ph(2-CF3)

3-73
Me
Me
H
2-OCH2CF3
Ph(2-F-6-Cl)

3-74
Me
Me
H
2-CN
Ph(2-F)

3-75
Me
Me
H
2-CN
Ph(2,6-F2)

3-76
Me
Me
H
2-CN
Ph(2-Cl)

3-77
Me
Me
H
2-CN
Ph(2-Me)

3-78
Me
Me
H
2-CN
Ph(2-CF3)

3-79
Me
Me
H
2-CN
Ph(2-F-6-Cl)

3-80
Me
Me
H
3-Cl
Ph(2-F)

3-81
Me
Me
H
3-Cl
Ph(2,6-F2)

3-82
Me
Me
H
3-Cl
Ph(2-Cl)

3-83
Me
Me
H
3-Cl
Ph(2-Me)

3-84
Me
Me
H
3-Cl
Ph(2-CF3)

3-85
Me
Me
H
3-Cl
Ph(2-F-6-Cl)

3-86
Me
Me
H
3-Br
Ph(2-F)

3-87
Me
Me
H
3-Br
Ph(2,6-F2)

3-88
Me
Me
H
3-Br
Ph(2-Cl)

3-89
Me
Me
H
3-Br
Ph(2-Me)

3-90
Me
Me
H
3-Br
Ph(2-CF3)

3-91
Me
Me
H
3-Br
Ph(2-F-6-Cl)

3-92
Me
Me
H
3-CF3
Ph(2-F)

3-93
Me
Me
H
3-CF3
Ph(2,6-F2)

3-94
Me
Me
H
3-CF3
P1-1(2-Cl)

3-95
Me
Me
H
3-CF3
Ph(2-Me)

3-96
Me
Me
H
3-CF3
Ph(2-CF3)

3-97
Me
Me
H
3-CF3
Ph(2-F-6-Cl)

3-98
Me
Me
H
2-OCF3
Ph(2-F)

3-99
Me
Me
H
2-OCF3
Ph(2,6-F2)

3-100
Me
Me
H
2-OCF3
Ph(2-Cl)

3-101
Me
Me
H
2-OCF3
Ph(2-Me)

3-102
Me
Me
H
2-OCF3
Ph(2-CF3)

3-103
Me
Me
H
2-OCF3
Ph(2-F-6-Cl)

3-104
Me
Me
H
3-OCHF2
Ph(2-F)

3-105
Me
Me
H
3-OCHF2
Ph(2,6-F2)

3-106
Me
Me
H
3-OCHF2
Ph(2-Cl)

3-107
Me
Me
H
3-OCHF2
Ph(2-Me)

3-108
Me
Me
H
3-OCHF2
Ph(2-CF3)

3-109
Me
Me
H
3-OCHF2
Ph(2-F-6-Cl)

3-110
Me
Me
H
3-OCH2CF3
Ph(2-F)

3-111
Me
Me
H
3-OCH2CF3
Ph(2,6-F2)

3-112
Me
Me
H
3-OCH2CF3
Ph(2-Cl)

3-113
Me
Me
H
3-OCH2CF3
Ph(2-Me)

3-114
Me
Me
H
3-OCH2CF3
Ph(2-CF3)

3-115
Me
Me
H
3-OCH2CF3
Ph(2-F-6-Cl)

3-116
Me
Me
H
3-CN
Ph(2-F)

3-117
Me
Me
H
3-CN
Ph(2,6-F2)

3-118
Me
Me
H
3-CN
Ph(2-Cl)

3-119
Me
Me
H
3-CN
Ph(2-Me)

3-120
Me
Me
H
3-CN
Ph(2-CF3)

3-121
Me
Me
H
3-CN
Ph(2-F-6-Cl)

3-122
Me
Me
H
4-Cl
Ph(2-F)

3-123
Me
Me
H
4-Cl
Ph(2,6-F2)

3-124
Me
Me
H
4-Cl
Ph(2-Cl)

3-125
Me
Me
H
4-Cl
Ph(2-Me)

3-126
Me
Me
H
4-Cl
Ph(2-CF3)

3-127
Me
Me
H
4-Cl
Ph(2-F-6-Cl)

3-128
Me
Me
H
4-Br
Ph(2-F)

3-129
Me
Me
H
4-Br
Ph(2,6-F2)

3-130
Me
Me
H
4-Br
Ph(2-Cl)

3-131
Me
Me
H
4-Br
Ph(2-Me)

3-132
Me
Me
H
4-Br
Ph(2-CF3)

3-133
Me
Me
H
4-Br
Ph(2-F-6-Cl)

3-134
Me
Me
H
4-CF3
Ph(2-F)

3-135
Me
Me
H
4-CF3
Ph(2,6-F2)

3-136
Me
Me
H
4-CF3
Ph(2-Cl)

3-137
Me
Me
H
4-CF3
Ph(2-Me)

3-138
Me
Me
H
4-CF3
Ph(2-CF3)

3-139
Me
Me
H
4-CF3
Ph(2-F-6-Cl)

3-140
Me
Me
H
4-OCF3
Ph(2-F)

3-141
Me
Me
H
4-OCF3
Ph(2,6-F2)

3-142
Me
Me
H
4-OCF3
Ph(2-Cl)

3-143
Me
Me
H
4-OCF3
Ph(2-Me)

3-144
Me
Me
H
4-OCF3
Ph(2-CF3)

3-145
Me
Me
H
4-OCF3
Ph(2-F-6-Cl)

3-146
Me
Me
H
4-OCHF2
Ph(2-F)

3-147
Me
Me
H
4-OCHF2
Ph(2,6-F2)

3-148
Me
Me
H
4-OCHF2
Ph(2-Cl)

3-149
Me
Me
H
4-OCHF2
Ph(2-Me)

3-150
Me
Me
H
4-OCHF2
Ph(2-CF3)

3-151
Me
Me
H
4-OCHF2
Ph(2-F-6-Cl)

3-152
Me
Me
H
4-OCH2CF3
Ph(2-F)

3-153
Me
Me
H
4-OCH2CF3
Ph(2,6-F2)

3-154
Me
Me
H
4-OCH2CF3
Ph(2-Cl)

3-155
Me
Me
H
4-OCH2CF3
Ph(2-Me)

3-156
Me
Me
H
4-OCH2CF3
Ph(2-CF3)

3-157
Me
Me
H
4-OCH2CF3
Ph(2-F-6-Cl)

3-158
Me
Me
H
4-CN
Ph(2-F)

3-159
Me
Me
H
4-CN
Ph(2,6-F2)

3-160
Me
Me
H
4-CN
Ph(2-Cl)

3-161
Me
Me
H
4-CN
Ph(2-Me)

3-162
Me
Me
H
4-CN
Ph(2-CF3)

3-163
Me
Me
H
4-CN
Ph(2-F-6-Cl)

3-164
Me
Me
H
5-Cl
Ph(2-F)

3-165
Me
Me
H
5-Cl
Ph(2,6-F2)

3-166
Me
Me
H
5-Cl
Ph(2-Cl)

3-167
Me
Me
H
5-Cl
Ph(2-Me)

3-168
Me
Me
H
5-Cl
Ph(2-CF3)

3-169
Me
Me
H
5-Cl
Ph(2-F-6-Cl)

3-170
Me
Me
H
5-Br
Ph(2-F)

3-171
Me
Me
H
5-Br
Ph(2,6-F2)

3-172
Me
Me
H
5-Br
Ph(2-Cl)

3-173
Me
Me
H
5-Br
Ph(2-Me)

3-174
Me
Me
H
5-Br
Ph(2-CF3)

3-175
Me
Me
H
5-Br
Ph(2-F-6-Cl)

3-176
Me
Me
H
5-CF3
Ph(2-F)

3-177
Me
Me
H
5-CF3
Ph(2,6-F2)

3-178
Me
Me
H
5-CF3
Ph(2-Cl)

3-179
Me
Me
H
5-CF3
Ph(2-Me)

3-180
Me
Me
H
5-CF3
Ph(2-CF3)

3-181
Me
Me
H
5-CF3
Ph(2-F-6-Cl)

3-182
Me
Me
H
5-OCF3
Ph(2-F)

3-183
Me
Me
H
5-OCF3
Ph(2,6-F2)

3-184
Me
Me
H
5-OCF3
Ph(2-Cl)

3-185
Me
Me
H
5-OCF3
Ph(2-Me)

3-186
Me
Me
H
5-OCF3
Ph(2-CF3)

3-187
Me
Me
H
5-OCF3
Ph(2-F-6-Cl)

3-188
Me
Me
H
5-OCHF2
Ph(2-F)

3-189
Me
Me
H
5-OCHF2
Ph(2,6-F2)

3-190
Me
Me
H
5-OCHF2
Ph(2-Cl)

3-191
Me
Me
H
5-OCHF2
Ph(2-Me)

3-192
Me
Me
H
5-OCHF2
Ph(2-CF3)

3-193
Me
Me
H
5-OCHF2
Ph(2-F-6-Cl)

3-194
Me
Me
H
5-OCH2CF3
Ph(2-F)

3-195
Me
Me
H
5-OCH2CF3
Ph(2,6-F2)

3-196
Me
Me
H
5-OCH2CF3
Ph(2-Cl)

3-197
Me
Me
H
5-OCH2CF3
Ph(2-Me)

3-198
Me
Me
H
5-OCH2CF3
Ph(2-CF3)

3-199
Me
Me
H
5-OCH2CF3
Ph(2-F-6-Cl)

3-200
Me
Me
H
5-CN
Ph(2-F)

3-201
Me
Me
H
5-CN
Ph(2,6-F2)

3-202
Me
Me
H
5-CN
Ph(2-Cl)

3-203
Me
Me
H
5-CN
Ph(2-Me)

3-204
Me
Me
H
5-CN
Ph(2-CF3)

3-205
Me
Me
H
5-CN
Ph(2-F-6-Cl)

3-206
Me
Me
H
6-Cl
Ph(2-F)

3-207
Me
Me
H
6-Cl
Ph(2,6-F2)

3-208
Me
Me
H
6-Cl
Ph(2-Cl)

3-209
Me
Me
H
6-Cl
Ph(2-Me)

3-210
Me
Me
H
6-Cl
Ph(2-CF3)

3-211
Me
Me
H
6-Cl
Ph(2-F-6-Cl)

3-212
Me
Me
H
6-Br
Ph(2-F)

3-213
Me
Me
H
6-Br
Ph(2,6-F2)

3-214
Me
Me
H
6-Br
Ph(2-Cl)

3-215
Me
Me
H
6-Br
Ph(2-Me)

3-216
Me
Me
H
6-Br
Ph(2-CF3)

3-217
Me
Me
H
6-Br
Ph(2-F-6-Cl)

3-218
Me
Me
H
6-CF3
Ph(2-F)

3-219
Me
Me
H
6-CF3
Ph(2,6-F2)

3-220
Me
Me
H
6-CF3
Ph(2-Cl)

3-221
Me
Me
H
6-CF3
Ph(2-Me)

3-222
Me
Me
H
6-CF3
Ph(2-CF3)

3-223
Me
Me
H
6-CF3
Ph(2-F-6-Cl)

3-224
Me
Me
H
6-OCF3
Ph(2-F)

3-225
Me
Me
H
6-OCF3
Ph(2,6-F2)

3-226
Me
Me
H
6-OCF3
Ph(2-Cl)

3-227
Me
Me
H
6-OCF3
Ph(2-Me)

3-228
Me
Me
H
6-OCF3
Ph(2-CF3)

3-229
Me
Me
H
6-OCF3
Ph(2-F-6-Cl)

3-230
Me
Me
H
6-OCHF2
Ph(2-F)

3-231
Me
Me
H
6-OCHF2
Ph(2,6-F2)

3-232
Me
Me
H
6-OCHF2
Ph(2-Cl)

3-233
Me
Me
H
6-OCHF2
Ph(2-Me)

3-234
Me
Me
H
6-OCHF2
Ph(2-CF3)

3-235
Me
Me
H
6-OCHF2
Ph(2-F-6-Cl)

3-236
Me
Me
H
6-OCH2CF3
Ph(2-F)

3-237
Me
Me
H
6-OCH2CF3
Ph(2,6-F2)

3-238
Me
Me
H
6-OCH2CF3
Ph(2-Cl)

3-239
Me
Me
H
6-OCH2CF3
Ph(2-Me)

3-240
Me
Me
H
6-OCH2CF3
Ph(2-CF3)

3-241
Me
Me
H
6-OCH2CF3
Ph(2-F-6-Cl)

3-242
Me
Me
H
6-CN
Ph(2-F)

3-243
Me
Me
H
6-CN
Ph(2,6-F2)

3-244
Me
Me
H
6-CN
Ph(2-Cl)

3-245
Me
Me
H
6-CN
Ph(2-Me)

3-246
Me
Me
H
6-CN
Ph(2-CF3)

3-247
Me
Me
H
6-CN
Ph(2-F-6-Cl)

3-248
Me
Me
H
7-Cl
Ph(2-F)

3-249
Me
Me
H
7-Cl
Ph(2,6-F2)

3-250
Me
Me
H
7-Cl
Ph(2-Cl)

3-251
Me
Me
H
7-Cl
Ph(2-Me)

3-252
Me
Me
H
7-Cl
Ph(2-CF3)

3-253
Me
Me
H
7-Cl
Ph(2-F-6-Cl)

3-254
Me
Me
H
7-Br
Ph(2-F)

3-255
Me
Me
H
7-Br
Ph(2,6-F2)

3-256
Me
Me
H
7-Br
Ph(2-Cl)

3-257
Me
Me
H
7-Br
Ph(2-Me)

3-258
Me
Me
H
7-Br
Ph(2-CF3)

3-259
Me
Me
H
7-Br
Ph(2-F-6-Cl)

3-260
Me
Me
H
7-CF3
Ph(2-F)

3-261
Me
Me
H
7-CF3
Ph(2,6-F2)

3-262
Me
Me
H
7-CF3
Ph(2-Cl)

3-263
Me
Me
H
7-CF3
Ph(2-Me)

3-264
Me
Me
H
7-CF3
Ph(2-CF3)

3-265
Me
Me
H
7-CF3
Ph(2-F-6-Cl)

3-266
Me
Me
H
7-OCF3
Ph(2-F)

3-267
Me
Me
H
7-OCF3
Ph(2,6-F2)

3-268
Me
Me
H
7-OCF3
Ph(2-Cl)

3-269
Me
Me
H
7-OCF3
Ph(2-Me)

3-270
Me
Me
H
7-OCF3
Ph(2-CF3)

3-271
Me
Me
H
7-OCF3
Ph(2-F-6-Cl)

3-272
Me
Me
H
7-OCHF2
Ph(2-F)

3-273
Me
Me
H
7-OCHF2
Ph(2,6-F2)

3-274
Me
Me
H
7-OCHF2
Ph(2-Cl)

3-275
Me
Me
H
7-OCHF2
Ph(2-Me)

3-276
Me
Me
H
7-OCHF2
Ph(2-CF3)

3-277
Me
Me
H
7-OCHF2
Ph(2-F-6-Cl)

3-278
Me
Me
H
7-OCH2CF3
Ph(2-F)

3-279
Me
Me
H
7-OCH2CF3
Ph(2,6-F2)

3-280
Me
Me
H
7-OCH2CF3
Ph(2-Cl)

3-281
Me
Me
H
7-OCH2CF3
Ph(2-Me)

3-282
Me
Me
H
7-OCH2CF3
Ph(2-CF3)

3-283
Me
Me
H
7-OCH2CF3
Ph(2-F-6-Cl)

3-284
Me
Me
H
7-CN
Ph(2-F)

3-235
Me
Me
H
7-CN
Ph(2,6-F2)

3-286
Me
Me
H
7-CN
Ph(2-Cl)

3-287
Me
Me
H
7-CN
Ph(2-Me)

3-288
Me
Me
H
7-CN
Ph(2-CF3)

3-289
Me
Me
H
7-CN
Ph(2-F-6-Cl)

3-290
Me
Me
H
2-Me-4-Cl
Ph(2-F)

3-291
Me
Me
H
2-Me-4-Cl
Ph(2,6-F2)

3-292
Me
Me
H
2-Me-4-Cl
Ph(2-Cl)

3-293
Me
Me
H
2-Me-4-Cl
P142-Me)

3-294
Me
Me
H
2-Me-4-Cl
Ph(2-CF3)

3-295
Me
Me
H
2-Me-4-Cl
Ph(2-F-6-Cl)

3-296
Me
Me
H
3-Me-4-Cl
Ph(2-F)

3-297
Me
Me
H
3-Me-4-Cl
Ph(2,6-F2)

3-298
Me
Me
H
3-Me-4-Cl
P142-Cl)

3-299
Me
Me
H
3-Me-4-Cl
Ph(2-Me)

3-300
Me
Me
H
3-Me-4-Cl
Ph(2-CF3)

3-301
Me
Me
H
3-Me-4-Cl
Ph(2-F-6-Cl)

3-302
Me
Me
H
5-Me-6-Cl
Ph(2-F)

3-303
Me
Me
H
5-Me-6-Cl
Ph(2,6-F2)

3-304
Me
Me
H
5-Me-6-Cl
Ph(2-Cl)

3-305
Me
Me
H
5-Me-6-Cl
Ph(2-Me)

3-306
Me
Me
H
5-Me-6-Cl
Ph(2-CF3)

3-307
Me
Me
H
5-Me-6-Cl
Ph(2-F-6-Cl)

3-308
Me
Me
H
6-Me-5-Cl
Ph(2-F)

3-309
Me
Me
H
6-Me-5-Cl
Ph(2,6-F2)

3-310
Me
Me
H
6-Me-5-Cl
Ph(2-C1)

3-311
Me
Me
H
6-Me-5-Cl
Ph(2-Me)

3-312
Me
Me
H
6-Me-5-Cl
Ph(2-CF3)

3-313
Me
Me
H
6-Me-5-Cl
Ph(2-F-6-Cl)

3-314
Me
Me
H
2-Me-4-Br
Ph(2-F)

3-315
Me
Me
H
2-Me-4-Br
Ph(2,6-F2)

3-316
Me
Me
H
2-Me-4-Br
Ph(2-Cl)

3-317
Me
Me
H
2-Me-4-Br
Ph(2-Me)

3-318
Me
Me
H
2-Me-4-Br
Ph(2-CF3)

3-319
Me
Me
H
2-Me-4-Br
Ph(2-F-6-Cl)

3-320
Me
Me
H
3-Me-4-Br
Ph(2-F)

3-321
Me
Me
H
3-Me-4-Br
Ph(2,6-F2)

3-322
Me
Me
H
3-Me-4-Br
Ph(2-Cl)

3-323
Me
Me
H
3-Me-4-Br
Ph(2-Me)

3-324
Me
Me
H
3-Me-4-Br
Ph(2-CF3)

3-325
Me
Me
H
3-Me-4-Br
Ph(2-F-6-Cl)

3-326
Me
Me
H
5-Me-6-Br
Ph(2-F)

3-327
Me
Me
H
5-Me-6-Br
Ph(2,6-F2)

3-328
Me
Me
H
5-Me-6-Br
Ph(2-Cl)

3-329
Me
Me
H
5-Me-6-Br
Ph(2-Me)

3-330
Me
Me
H
5-Me-6-Br
Ph(2-CF3)

3-331
Me
Me
H
5-Me-6-Br
Ph(2-F-6-Cl)

3-332
Me
Me
H
6-Me-5-Br
Ph(2-F)

3-333
Me
Me
H
6-Me-5-Br
Ph(2,6-F2)

3-334
Me
Me
H
6-Me-5-Br
Ph(2-Cl)

3-335
Me
Me
H
6-Me-5-Br
Ph(2-Me)

3-336
Me
Me
H
6-Me-5-Br
Ph(2-CF3)

3-337
Me
Me
H
6-Me-5-Br
Ph(2-F-6-Cl)

3-338
Me
Me
H
2-Me-4-CF3
Ph(2-F)

3-339
Me
Me
H
2-Me-4-CF3
Ph(2,6-F2)

3-340
Me
Me
H
2-Me-4-CF3
Ph(2-Cl)

3-341
Me
Me
H
2-Me-4-CF3
Ph(2-Me)

3-342
Me
Me
H
2-Me-4-CF3
Ph(2-CF3)

3-343
Me
Me
H
2-Me-4-CF3
Ph(2-F-6-Cl)

3-344
Me
Me
H
3-Me-4-CF3
Ph(2-F)

3-345
Me
Me
H
3-Me-4-CF3
Ph(2,6-F2)

3-346
Me
Me
H
3-Me-4-CF3
Ph(2-Cl)

3-347
Me
Me
H
3-Me-4-CF3
Ph(2-Me)

3-348
Me
Me
H
3-Me-4-CF3
Ph(2-CF3)

3-349
Me
Me
H
3-Me-4-CF3
Ph(2-F-6-Cl)

3-350
Me
Me
H
5-Me-6-CF3
Ph(2-F)

3-351
Me
Me
H
5-Me-6-CF3
Ph(2,6-F2)

3-352
Me
Me
H
5-Me-6-CF3
Ph(2-Cl)

3-353
Me
Me
H
5-Me-6-CF3
Ph(2-Me)

3-354
Me
Me
H
5-Me-6-CF3
Ph(2-CF3)

3-355
Me
Me
H
5-Me-6-CF3
Ph(2-F-6-Cl)

3-356
Me
Me
H
6-Me-5-CF3
Ph(2-F)

3-357
Me
Me
H
6-Me-5-CF3
Ph(2,6-F2)

3-358
Me
Me
H
6-Me-5-CF3
Ph(2-Cl)

3-359
Me
Me
H
6-Me-5-CF3
Ph(2-Me)

3-360
Me
Me
H
6-Me-5-CF3
Ph(2-CF3)

3-361
Me
Me
H
6-Me-5-CF3
Ph(2-F-6-Cl)

3-362
Me
Me
H
2-Me-4-OCF3
Ph(2-F)

3-363
Me
Me
H
2-Me-4-OCF3
Ph(2,6-F2)

3-364
Me
Me
H
2-Me-4-OCF3
Ph(2-Cl)

3-365
Me
Me
H
2-Me-4-OCF3
Ph(2-Me)

3-366
Me
Me
H
2-Me-4-OCF3
Ph(2-CF3)

3-367
Me
Me
H
2-Me-4-OCF3
Ph(2-F-6-Cl)

3-368
Me
Me
H
3-Me-4-OCF3
Ph(2-F)

3-369
Me
Me
H
3-Me-4-OCF3
Ph(2,6-F2)

3-370
Me
Me
H
3-Me-4-OCF3
Ph(2-Cl)

3-371
Me
Me
H
3-Me-4-OCF3
Ph(2-Me)

3-372
Me
Me
H
3-Me-4-OCF3
Ph(2-CF3)

3-373
Me
Me
H
3-Me-4-OCF3
Ph(2-F-6-Cl)

3-374
Me
Me
H
5-Me-6-OCF3
Ph(2-F)

3-375
Me
Me
H
5-Me-6-OCF3
Ph(2,6-F2)

3-376
Me
Me
H
5-Me-6-OCF3
Ph(2-Cl)

3-377
Me
Me
H
5-Me-6-OCF3
Ph(2-Me)

3-378
Me
Me
H
5-Me-6-OCF3
Ph(2-CF3)

3-379
Me
Me
H
5-Me-6-OCF3
Ph(2-F-6-Cl)

3-380
Me
Me
H
6-Me-5-OCF3
Ph(2-F)

3-381
Me
Me
H
6-Me-5-OCF3
Ph(2,6-F2)

3-382
Me
Me
H
6-Me-5-OCF3
Ph(2-Cl)

3-383
Me
Me
H
6-Me-5-OCF3
Ph(2-Me)

3-384
Me
Me
H
6-Me-5-OCF3
Ph(2-CF3)

3-385
Me
Me
H
6-Me-5-OCF3
Ph(2-F-6-Cl)

3-386
Me
Me
H
2-Me-4-OCHF2
Ph(2-F)

3-387
Me
Me
H
2-Me-4-OCHF2
Ph(2,6-F2)

3-388
Me
Me
H
2-Me-4-OCHF2
Ph(2-Cl)

3-389
Me
Me
H
2-Me-4-OCHF2
Ph(2-Me)

3-390
Me
Me
H
2-Me-4-OCHF2
Ph(2-CF3)

3-391
Me
Me
H
2-Me-4-OCHF2
Ph(2-F-6-Cl)

3-392
Me
Me
H
3-Me-4-OCHF2
Ph(2-F)

3-393
Me
Me
H
3-Me-4-OCHF2
Ph(2,6-F2)

3-394
Me
Me
H
3-Me-4-OCHF2
Ph(2-Cl)

3-395
Me
Me
H
3-Me-4-OCHF2
Ph(2-Me)

3-396
Me
Me
H
3-Me-4-OCHF2
Ph(2-CF3)

3-397
Me
Me
H
3-Me-4-OCHF2
Ph(2-F-6-Cl)

3-398
Me
Me
H
5-Me-6-OCHF2
Ph(2-F)

3-399
Me
Me
H
5-Me-6-OCHF2
Ph(2,6-F2)

3-400
Me
Me
H
5-Me-6-OCHF2
Ph(2-Cl)

3-401
Me
Me
H
5-Me-6-OCHF2
Ph(2-Me)

3-402
Me
Me
H
5-Me-6-OCHF2
Ph(2-CF3)

3-403
Me
Me
H
5-Me-6-OCHF2
Ph(2-F-6-Cl)

3-404
Me
Me
H
6-Me-5-OCHF2
Ph(2-F)

3-405
Me
Me
H
6-Me-5-OCHF2
Ph(2,6-F2)

3-406
Me
Me
H
6-Me-5-OCHF2
Ph(2-Cl)

3-407
Me
Me
H
6-Me-5-OCHF2
Ph(2-Me)

3-408
Me
Me
H
6-Me-5-OCHF2
Ph(2-CF3)

3-409
Me
Me
H
6-Me-5-OCHF2
Ph(2-F-6-Cl)

3-410
Me
Me
H
2-Me-4-OCH2CF3
Ph(2-F)

3-411
Me
Me
H
2-Me-4-OCH2CF3
Ph(2,6-F2)

3-412
Me
Me
H
2-Me-4-OCH2CF3
Ph(2-Cl)

3-413
Me
Me
H
2-Me-4-OCH2CF3
Ph(2-Me)

3-414
Me
Me
H
2-Me-4-OCH2CF3
Ph(2-CF3)

3-415
Me
Me
H
2-Me-4-OCH2CF3
Ph(2-F-6-Cl)

3-416
Me
Me
H
3-Me-4-OCH2CF3
Ph(2-F)

3-417
Me
Me
H
3-Me-4-OCH2CF3
Ph(2,6-F2)

3-418
Me
Me
H
3-Me-4-OCH2CF3
Ph(2-Cl)

3-419
Me
Me
H
3-Me-4-OCH2CF3
Ph(2-Me)

3-420
Me
Me
H
3-Me-4-OCH2CF3
Ph(2-CF3)

3-421
Me
Me
H
3-Me-4-OCH2CF3
Ph(2-F-6-Cl)

3-422
Me
Me
H
5-Me-6-OCH2CF3
Ph(2-F)

3-423
Me
Me
H
5-Me-6-OCH2CF3
Ph(2,6-F2)

3-424
Me
Me
H
5-Me-6-OCH2CF3
Ph(2-Cl)

3-425
Me
Me
H
5-Me-6-OCH2CF3
Ph(2-Me)

3-426
Me
Me
H
5-Me-6-OCH2CF3
Ph(2-CF3)

3-427
Me
Me
H
5-Me-6-OCH2CF3
Ph(2-F-6-Cl)

3-428
Me
Me
H
6-Me-5-OCH2CF3
Ph(2-F)

3-429
Me
Me
H
6-Me-5-OCH2CF3
Ph(2,6-F2)

3-430
Me
Me
H
6-Me-5-OCH2CF3
Ph(2-Cl)

3-431
Me
Me
H
6-Me-5-OCH2CF3
Ph(2-Me)

3-432
Me
Me
H
6-Me-5-OCH2CF3
Ph(2-CF3)

3-433
Me
Me
H
6-Me-5-OCH2CF3
Ph(2-F-6-Cl)

3-434
Me
Me
H
2,4-Cl2
Ph(2-F)

3-435
Me
Me
H
2,4-Cl2
Ph(2,6-F2)

3-436
Me
Me
H
2,4-Cl2
Ph(2-Cl)

3-437
Me
Me
H
2,4-Cl2
Ph(2-Me)

3-438
Me
Me
H
2,4-Cl2
Ph(2-CF3)

3-439
Me
Me
H
2,4-Cl2
Ph(2-F-6-Cl)

3-440
Me
Me
H
3,4-Cl2
Ph(2-F)

3-441
Me
Me
H
3,4-Cl2
Ph(2,6-F2)

3-442
Me
Me
H
3,4-Cl2
Ph(2-Cl)

3-443
Me
Me
H
3,4-Cl2
Ph(2-Me)

3-444
Me
Me
H
3,4-Cl2
Ph(2-CF3)

3-445
Me
Me
H
3,4-Cl2
Ph(2-F-6-Cl)

3-446
Me
Me
H
5,6-Cl2
Ph(2-F)

3-447
Me
Me
H
5,6-Cl2
Ph(2,6-F2)

3-448
Me
Me
H
5,6-Cl2
Ph(2-Cl)

3-449
Me
Me
H
5,6-Cl2
Ph(2-Me)

3-450
Me
Me
H
5,6-Cl2
Ph(2-CF3)

3-451
Me
Me
H
5,6-Cl2
Ph(2-F-6-Cl)

3-452
Me
Me
H
2-Cl-4-Br
Ph(2-F)

3-453
Me
Me
H
2-Cl-4-Br
Ph(2,6-F2)

3-454
Me
Me
H
2-Cl-4-Br
Ph(2-Cl)

3-455
Me
Me
H
2-Cl-4-Br
Ph(2-Me)

3-456
Me
Me
H
2-Cl-4-Br
Ph(2-CF3)

3-457
Me
Me
H
2-Cl-4-Br
Ph(2-F-6-Cl)

3-458
Me
Me
H
3-Cl-4-Br
Ph(2-F)

3-459
Me
Me
H
3-Cl-4-Br
Ph(2,6-F2)

3-460
Me
Me
H
3-Cl-4-Br
Ph(2-Cl)

3-461
Me
Me
H
3-Cl-4-Br
Ph(2-Me)

3-462
Me
Me
H
3-Cl-4-Br
Ph(2-CF3)

3-463
Me
Me
H
3-Cl-4-Br
Ph(2-F-6-Cl)

3-464
Me
Me
H
5-Cl-6-Br
Ph(2-F)

3-465
Me
Me
H
5-Cl-6-Br
Ph(2,6-F2)

3-466
Me
Me
H
S-Cl-6-Br
Ph(2-Cl)

3-467
Me
Me
H
5-Cl-6-Br
Ph(2-Me)

3-468
Me
Me
H
5-Cl-6-Br
Ph(2-CF3)

3-469
Me
Me
H
5-Cl-6-Br
Ph(2-F-6-Cl)

3-470
Me
Me
H
6-Cl-5-Br
Ph(2-F)

3-471
Me
Me
H
6-Cl-5-Br
Ph(2,6-F2)

3-472
Me
Me
H
6-Cl-5-Br
Ph(2-Cl)

3-473
Me
Me
H
6-Cl-5-Br
Ph(2-Me)

3-474
Me
Me
H
6-Cl-5-Br
Ph(2-CF3)

3-475
Me
Me
H
6-Cl-5-Br
Ph(2-F-6-Cl)

3-476
Me
Me
H
2-C1-4-CF3
Ph(2-F)

3-477
Me
Me
H
2-Cl-4-CF3
Ph(2,6-F2)

3-478
Me
Me
H
2-Cl-4-CF3
Ph(2-Cl)

3-479
Me
Me
H
2-Cl-4-CF3
Ph(2-Me)

3-480
Me
Me
H
2-Cl-4-CF3
Ph(2-CF3)

3-481
Me
Me
H
2-Cl-4-CF3
Ph(2-F-6-Cl)

3-482
Me
Me
H
3-Cl-4-CF3
Ph(2-F)

3-483
Me
Me
H
3-Cl-4-CF3
Ph(2,6-F2)

3-484
Me
Me
H
3-Cl-4-CF3
Ph(2-Cl)

3-485
Me
Me
H
3-Cl-4-CF3
Ph(2-Me)

3-486
Me
Me
H
3-Cl-4-CF3
Ph(2-CF3)

3-487
Me
Me
H
3-Cl-4-CF3
Ph(2-F-6-Cl)

3-488
Me
Me
H
5-Cl-6-CF3
Ph(2-F)

3-489
Me
Me
H
5-Cl-6-CF3
Ph(2,6-F2)

3-490
Me
Me
H
5-Cl-6-CF3
Ph(2-Cl)

3-491
Me
Me
H
5-Cl-6-CF3
Ph(2-Me)

3-492
Me
Me
H
5-Cl-6-CF3
Ph(2-CF3)

3-493
Me
Me
H
5-Cl-6-CF3
Ph(2-F-6-Cl)

3-494
Me
Me
H
6-Cl-5-CF3
Ph(2-F)

3-495
Me
Me
H
6-Cl-5-CF3
Ph(2,6-F2)

3-496
Me
Me
H
6-Cl-5-CF3
Ph(2-Cl)

3-497
Me
Me
H
6-Cl-5-CF3
Ph(2-Me)

3-498
Me
Me
H
6-Cl-5-CF3
Ph(2-CF3)

3-499
Me
Me
H
6-Cl-5-CF3
Ph(2-F-6-Cl)

3-500
Me
Me
H
2-Cl-4-OCF3
Ph(2-F)

3-501
Me
Me
H
2-Cl-4-OCF3
Ph(2,6-F2)

3-502
Me
Me
H
2-Cl-4-OCF3
Ph(2-Cl)

3-503
Me
Me
H
2-Cl-4-OCF3
Ph(2-Me)

3-504
Me
Me
H
2-Cl-4-OCF3
Ph(2-CF3)

3-505
Me
Me
H
2-Cl-4-OCF3
Ph(2-F-6-Cl)

3-506
Me
Me
H
3-Cl-4-OCF3
Ph(2-F)

3-507
Me
Me
H
3-Cl-4-OCF3
Ph(2,6-F2)

3-508
Me
Me
H
3-Cl-4-OCF3
Ph(2-Cl)

3-509
Me
Me
H
3-Cl-4-OCF3
Ph(2-Me)

3-510
Me
Me
H
3-Cl-4-OCF3
Ph(2-CF3)

3-511
Me
Me
H
3-Cl-4-OCF3
Ph(2-F-6-Cl)

3-512
Me
Me
H
5-Cl-6-OCF3
Ph(2-F)

3-513
Me
Me
H
5-Cl-6-OCF3
Ph(2,6-F2)

3-514
Me
Me
H
5-Cl-6-OCF3
Ph(2-Cl)

3-515
Me
Me
H
5-Cl-6-OCF3
Ph(2-Me)

3-516
Me
Me
H
5-Cl-6-OCF3
Ph(2-CF3)

3-517
Me
Me
H
5-Cl-6-OCF3
Ph(2-F-6-Cl)

3-518
Me
Me
H
6-Cl-5-OCF3
Ph(2-F)

3-519
Me
Me
H
6-Cl-5-OCF3
Ph(2,6-F2)

3-520
Me
Me
H
6-Cl-5-OCF3
Ph(2-Cl)

3-521
Me
Me
H
6-Cl-5-OCF3
Ph(2-Me)

3-522
Me
Me
H
6-Cl-5-OCF3
Ph(2-CF3)

3-523
Me
Me
H
6-Cl-5-OCF3
Ph(2-F-6-Cl)

3-524
Me
Me
H
2-Cl-4-OCHF2
Ph(2-F)

3-525
Me
Me
H
2-Cl-4-OCHF2
Ph(2,6-F2)

3-526
Me
Me
H
2-Cl-4-OCHF2
Ph(2-Cl)

3-527
Me
Me
H
2-Cl-4-OCHF2
Ph(2-Me)

3-528
Me
Me
H
2-Cl-4-OCHF2
Ph(2-CF3)

3-529
Me
Me
H
2-Cl-4-OCHF2
Ph(2-F-6-Cl)

3-530
Me
Me
H
3-Cl-4-OCHF2
Ph(2-F)

3-531
Me
Me
H
3-Cl-4-OCHF2
Ph(2,6-F2)

3-532
Me
Me
H
3-Cl-4-OCHF2
Ph(2-Cl)

3-533
Me
Me
H
3-Cl-4-OCHF2
Ph(2-Me)

3-534
Me
Me
H
3-Cl-4-OCHF2
Ph(2-CF3)

3-535
Me
Me
H
3-Cl-4-OCHF2
Ph(2-F-6-Cl)

3-536
Me
Me
H
5-Cl-6-OCHF2
Ph(2-F)

3-537
Me
Me
H
5-Cl-6-OCHF2
Ph(2,6-F2)

3-538
Me
Me
H
5-Cl-6-OCHF2
Ph(2-Cl)

3-539
Me
Me
H
5-Cl-6-OCHF2
Ph(2-Me)

3-540
Me
Me
H
5-Cl-6-OCHF2
Ph(2-CF3)

3-541
Me
Me
H
5-Cl-6-OCHF2
Ph(2-F-6-Cl)

3-542
Me
Me
H
6-Cl-5-OCHF2
Ph(2-F)

3-543
Me
Me
H
6-Cl-5-OCHF2
Ph(2,6-F2)

3-544
Me
Me
H
6-Cl-5-OCHF2
Ph(2-Cl)

3-545
Me
Me
H
6-Cl-5-OCHF2
Ph(2-Me)

3-546
Me
Me
H
6-Cl-5-OCHF2
Ph(2-CF3)

3-547
Me
Me
H
6-Cl-5-OCHF2
Ph(2-F-6-Cl)

3-548
Me
Me
H
2-Cl-4-OCH2CF3
Ph(2-F)

3-549
Me
Me
H
2-Cl-4-OCH2CF3
Ph(2,6-F2)

3-550
Me
Me
H
2-Cl-4-OCH2CF3
Ph(2-Cl)

3-551
Me
Me
H
2-Cl-4-OCH2CF3
Ph(2-Me)

3-552
Me
Me
H
2-Cl-4-OCH2CF3
Ph(2-CF3)

3-553
Me
Me
H
2-Cl-4-OCH2CF3
Ph(2-F-6-Cl)

3-554
Me
Me
H
3-Cl-4-OCH2CF3
Ph(2-F)

3-555
Me
Me
H
3-Cl-4-OCH2CF3
Ph(2,6-F2)

3-556
Me
Me
H
3-Cl-4-OCH2CF3
Ph(2-Cl)

3-557
Me
Me
H
3-Cl-4-OCH2CF3
Ph(2-Me)

3-558
Me
Me
H
3-Cl-4-OCH2CF3
Ph(2-CF3)

3-559
Me
Me
H
3-Cl-4-OCH2CF3
Ph(2-F-6-Cl)

3-560
Me
Me
H
5-Cl-6-OCH2CF3
Ph(2-F)

3-561
Me
Me
H
5-Cl-6-OCH2CF3
Ph(2,6-F2)

3-562
Me
Me
H
5-Cl-6-OCH2CF3
Ph(2-Cl)

3-563
Me
Me
H
5-Cl-6-OCH2CF3
Ph(2-Me)

3-564
Me
Me
H
5-Cl-6-OCH2CF3
Ph(2-CF3)

3-565
Me
Me
H
5-Cl-6-OCH2CF3
Ph(2-F-6-Cl)

3-566
Me
Me
H
6-Cl-5-OCH2CF3
Ph(2-F)

3-567
Me
Me
H
6-Cl-5-OCH2CF3
Ph(2,6-F2)

3-568
Me
Me
H
6-Cl-5-OCH2CF3
Ph(2-Cl)

3-569
Me
Me
H
6-Cl-5-OCH2CF3
Ph(2-Me)

3-570
Me
Me
H
6-Cl-5-OCH2CF3
Ph(2-CF3)

3-571
Me
Me
H
6-Cl-5-OCH2CF3
Ph(2-F-6-Cl)

[0243]

4

TABLE 4

Com-

Physical

pound

properties

No.
R1
R2
R3
X
B
(mp ° C.)

4-1
Me
Me
H
H
Ph

4-2
Me
Me
H
H
Ph(2-F)
114-116

4-3
Me
Me
H
H
Ph(2-Cl)

4-4
Me
Me
H
H
Ph(2-OMe)

4-5
Me
Me
H
H
Ph(2,6-F2)
170-172

4-6
Me
Me
H
H
Ph(2,6-Cl2)

4-7
Me
Me
H
H
Ph(2,6-OMe2)
128-130

4-8
Me
Me
H
6-Cl
Ph

4-9
Me
Me
H
6-Cl
Ph(2-F)

4-10
Me
Me
H
6-Cl
Ph(2-Cl)

4-11
Me
Me
H
6-Cl
Ph(2,6-F2)

4-12
Me
Me
H
6-Cl
Ph(2,6-Cl2)

4-13
Me
Me
H
6-Br
Ph

4-14
Me
Me
H
6-Br
Ph(2-F)

4-15
Me
Me
H
6-Br
Ph(2-Cl)

4-16
Me
Me
H
6-Br
Ph(2,6-F2)

4-17
Me
Me
H
6-Br
Ph(2,6-Cl2)

4-18
Me
Me
H
6-CF3
Ph(2,6-F2)

4-19
Me
Me
H
6-CN
Ph(2,6-F2)

4-20
Me
CN
H
H
Ph(2,6-F2)

4-21
Me
CO2Et
H
H
Ph(2,6-F2)

4-22
Me
CN
H
6-Cl
Ph(2,6-F2)

4-23
Me
CO2Et
H
6-Cl
Ph(2,6-F2)

4-24
Me
Et
H
H
Ph(2,6-F2)

4-25
Me
Me
COMe
H
Ph(2,6-F2)

4-26
Me
Me
CH2OMe
H
Ph(2,6-F2)

4-27
Me
Me
H
H
1-naphthyl

4-28
Me
Me
H
H
2-naphthyl

4-29
Me
Me
H
H
2-thienyl

4-30
Me
Me
H
H
3-thienyl

4-31
Me
Me
H
H
2-pyrazinyl

4-32
Me
Me
H
H
2-pyridyl

4-33
Me
Me
H
H
3-pyridyl

4-34
Me
Me
H
H
4-tri-
156-158

fluorometh-

yl-3-pyridyl

4-35
Me
Me
H
H
4-pyridyl

4-36
Me
Me
H
H
2-furyl

4-37
Me
Me
H
H
3-furyl

4-38
Me
Me
H
1-Cl
Ph(2-F)

4-39
Me
Me
H
1-Cl
Ph(2,6-F2)

4-40
Me
Me
H
1-Cl
Ph(2-Cl)

4-41
Me
Me
H
1-Cl
Ph(2-Me)

4-42
Me
Me
H
1-Cl
Ph(2-CF3)

4-43
Me
Me
H
1-Cl
Ph(2-F-6-Cl)

4-44
Me
Me
H
1-Me
Ph(2-F)

4-45
Me
Me
H
1-Me
Ph(2,6-F2)

4-46
Me
Me
H
1-Me
Ph(2-Cl)

4-47
Me
Me
H
1-Me
Ph(2-Me)

4-48
Me
Me
H
1-Me
Ph(2-CF3)

4-49
Me
Me
H
1-Me
Ph(2-F-6-Cl)

4-50
Me
Me
H
3-Cl
Ph(2-F)

4-51
Me
Me
H
3-Cl
Ph(2,6-F2)

4-52
Me
Me
H
3-Cl
Ph(2-Cl)

4-53
Me
Me
H
3-Cl
Ph(2-Me)

4-54
Me
Me
H
3-Cl
Ph(2-CF3)

4-55
Me
Me
H
3-Cl
Ph(2-F-6-Cl)

4-56
Me
Me
H
3-Me
Ph(2-F)

4-57
Me
Me
H
3-Me
Ph(2,6-F2)

4-58
Me
Me
H
3-Me
Ph(2-Cl)

4-59
Me
Me
H
3-Me
Ph(2-Me)

4-60
Me
Me
H
3-Me
Ph(2-CF3)

4-61
Me
Me
H
3-Me
Ph(2-F-6-Cl)

4-62
Me
Me
H
3-CF3
Ph(2-F)

4-63
Me
Me
H
3-CF3
Ph(2,6-F2)

4-64
Me
Me
H
3-CF3
Ph(2-Cl)

4-65
Me
Me
H
3-CF3
Ph(2-Me)

4-66
Me
Me
H
3-CF3
Ph(2-CF3)

4-67
Me
Me
H
3-CF3
Ph(2-F-6-Cl)

4-68
Me
Me
H
4-CF3
Ph(2-F)

4-69
Me
Me
H
4-CF3
Ph(2,6-F2)

4-70
Me
Me
H
4-CF3
Ph(2-Cl)

4-71
Me
Me
H
4-CF3
Ph(2-Me)

4-72
Me
Me
H
4-CF3
Ph(2-CF3)

4-73
Me
Me
H
4-CF3
Ph(2-F-6-Cl)

4-74
Me
Me
H
3-CN
Ph(2-F)

4-75
Me
Me
H
3-CN
Ph(2,6-F2)

4-76
Me
Me
H
3-CN
Ph(2-Cl)

4-77
Me
Me
H
3-CN
Ph(2-Me)

4-78
Me
Me
H
3-CN
Ph(2-CF3)

4-79
Me
Me
H
3-CN
Ph(2-F-6-Cl)

4-80
Me
Me
H
4-CN
Ph(2-F)

4-81
Me
Me
H
4-CN
Ph(2,6-F2)

4-82
Me
Me
H
4-CN
Ph(2-Cl)

4-83
Me
Me
H
4-CN
Ph(2-Me)

4-84
Me
Me
H
4-CN
Ph(2-CF3)

4-85
Me
Me
H
4-CN
Ph(2-F-6-Cl)

[0244]

5

TABLE 5

Physical properties

Compound No.
R1
R2
R3
X
B
(mp ° C.)

5-1
Me
Me
H
H
Ph

5-2
Me
Me
H
H
Ph(2-F)

5-3
Me
Me
H
H
Ph(2-Cl)

5-4
Me
Me
H
H
Ph(2-OMe)

5-5
Me
Me
H
H
Ph(2,6-F2)
108-110

5-6
Me
Me
H
H
Ph(2,6-Cl2)

5-7
Me
Me
H
H
Ph(2,6-OMe2)

5-8
Me
Me
H
5-Cl
Ph

5-9
Me
Me
H
5-Cl
Ph(2-F)
127-130

5-10
Me
Me
H
5-Cl
Ph(2-Cl)

5-11
Me
Me
H
5-Cl
Ph(2,6-F2)
129-131

5-12
Me
Me
H
5-Cl
Ph(2,6-Cl2)

5-13
Me
Me
H
5-Br
Ph

5-14
Me
Me
H
5-Br
Ph(2-F)
141-142

5-15
Me
Me
H
5-Br
Ph(2-Cl)

5-16
Me
Me
H
5-Br
Ph(2,6-F2)
145-147

5-17
Me
Me
H
5-Br
Ph(2,6-Cl2)

5-18
Me
Me
H
5-CF3
Ph(2,6-F2)

5-19
Me
Me
H
5-CN
Ph(2,6-F2)

5-20
Me
Me
H
3-Me
Ph(2,6-F2)
124-127

5-21
Me
CN
H
H
Ph(2,6-F2)

5-22
Me
CO2Et
H
H
Ph(2,6-F2)

5-23
Me
CN
H
5-Cl
Ph(2,6-F2)

5-24
Me
CO2Et
H
5-Cl
Ph(2,6-F2)

5-25
Me
Et
H
H
Ph(2,6-F2)

5-26
Me
Me
COMe
H
Ph(2,6-F2)

5-27
Me
Me
CH2OMe
H
Ph(2,6-F2)

5-28
Me
Me
H
H
1-naphthyl

5-29
Me
Me
H
H
2-naphthyl

5-30
Me
Me
H
H
2-thienyl

5-31
Me
Me
H
H
3-thienyl

5-32
Me
Me
H
H
2-pyrazinyl

5-33
Me
Me
H
H
2-pyridyl

5-34
Me
Me
H
H
3-pyridyl

5-35
Me
Me
H
H
4-trifluoro-methyl-3-pyridyl

5-36
Me
Me
H
H
4-pyridyl

5-37
Me
Me
H
H
2-furyl

5-38
Me
Me
H
H
3-furyl

5-39
Me
Me
H
3-Br
Ph(2,6-F2)

5-40
Me
Me
H
3-CF3
Ph(2,6-F2)

5-41
Me
Me
H
3-CN
Ph(2,6-F2)

5-42
Me
Me
H
5-Me
Ph(2,6-F2)

5-43
Me
Me
H
5-OSO2CF3
Ph(2-F)

5-44
Me
Me
H
5-OSO2CF3
Ph(2,6-F2)

5-45
Me
Me
H
5-OCH2CF3
Ph(2-F)

5-46
Me
Me
H
5-OCH2CF3
Ph(2,6-F2)

5-47
Me
Me
H
3-Cl
Ph(2-F)

5-48
Me
Me
H
3-Cl
Ph(2,6-F2)

5-49
Me
Me
H
3-Cl
Ph(2-Cl)

5-50
Me
Me
H
3-Cl
Ph(2-Me)

5-51
Me
Me
H
3-Cl
Ph(2-CF3)

5-52
Me
Me
H
3-Cl
Ph(2-F-6-Cl)

5-53
Me
Me
H
4-Cl
Ph(2-F)

5-54
Me
Me
H
4-Cl
Ph(2,6-F2)

5-55
Me
Me
H
4-Cl
Ph(2-Cl)

5-56
Me
Me
H
4-Cl
Ph(2-Me)

5-57
Me
Me
H
4-Cl
Ph(2-CF3)

5-58
Me
Me
H
4-Cl
Ph(2-F-6-Cl)

5-59
Me
Me
H
3-Br
Ph(2-F)

5-60
Me
Me
H
3-Br
Ph(2,6-F2)

5-61
Me
Me
H
3-Br
Ph(2-Cl)

5-62
Me
Me
H
3-Br
Ph(2-Me)

5-63
Me
Me
H
3-Br
Ph(2-CF3)

5-64
Me
Me
H
3-Br
Ph(2-F-6-Cl)

5-65
Me
Me
H
4-Br
Ph(2-F)
120-123

5-66
Me
Me
H
4-Br
Ph(2,6-F2)
218-220

5-67
Me
Me
H
4-Br
Ph(2-Cl)

5-68
Me
Me
H
4-Br
Ph(2-Me)

5-69
Me
Me
H
4-Br
Ph(2-CF3)

5-70
Me
Me
H
4-Br
Ph(2-F-6-Cl)

5-71
Me
Me
H
3-CF3
Ph(2-F)

5-72
Me
Me
H
3-CF3
Ph(2,6-F2)

5-73
Me
Me
H
3-CF3
Ph(2-Cl)

5-74
Me
Me
H
3-CF3
Ph(2-Me)

5-75
Me
Me
H
3-CF3
Ph(2-CF3)

5-76
Me
Me
H
3-CF3
Ph(2-F-6-Cl)

5-77
Me
Me
H
4-CF3
Ph(2-F)

5-78
Me
Me
H
4-CF3
Ph(2,6-F2)

5-79
Me
Me
H
4-CF3
Ph(2-Cl)

5-80
Me
Me
H
4-CF3
Ph(2-Me)

5-81
Me
Me
H
4-CF3
Ph(2-CF3)

5-82
Me
Me
H
4-CF3
Ph(2-F-6-Cl)

5-83
Me
Me
H
5-CF3
Ph(2-F)

5-84
Me
Me
H
5-CF3
Ph(2-Cl)

5-85
Me
Me
H
5-CF3
Ph(2,6-Cl2)

5-86
Me
Me
H
3-CN
Ph(2-F)

5-87
Me
Me
H
3-CN
Ph(2,6-F2)

5-88
Me
Me
H
3-CN
Ph(2-Cl)

5-89
Me
Me
H
3-CN
Ph(2-Me)

5-90
Me
Me
H
3-CN
Ph(2-CF3)

5-91
Me
Me
H
3-CN
Ph(2-F-6-Cl)

5-92
Me
Me
H
4-CN
Ph(2-F)

5-93
Me
Me
H
4-CN
Ph(2,6-F2)

5-94
Me
Me
H
4-CN
Ph(2-Cl)

5-95
Me
Me
H
4-CN
Ph(2-Me)

5-96
Me
Me
H
4-CN
Ph(2-CF3)

5-97
Me
Me
H
4-CN
Ph(2-F-6-Cl)

5-98
Me
Me
H
5-CN
Ph(2-F)

5-99
Me
Me
H
5-CN
Ph(2-Cl)

5-100
Me
Me
H
5-CN
Ph(2,6-Cl2)

5-101
Me
Me
H
3-OCF3
Ph(2-F)

5-102
Me
Me
H
3-OCF3
Ph(2,6-F2)

5-103
Me
Me
H
3-OCF3
Ph(2-Cl)

5-104
Me
Me
H
3-OCF3
Ph(2-Me)

5-105
Me
Me
H
3-OCF3
Ph(2-CF3)

5-106
Me
Me
H
3-OCF3
Ph(2-F-6-Cl)

5-107
Me
Me
H
4-OCF3
Ph(2-F)

5-108
Me
Me
H
4-OCF3
Ph(2,6-F2)

5-109
Me
Me
H
4-OCF3
Ph(2-Cl)

5-110
Me
Me
H
4-OCF3
Ph(2-Me)

5-111
Me
Me
H
4-OCF3
Ph(2-CF3)

5-112
Me
Me
H
4-OCF3
Ph(2-F-6-Cl)

5-113
Me
Me
H
5-OCF3
Ph(2-F)

5-114
Me
Me
H
5-OCF3
Ph(2,6-F2)

5-115
Me
Me
H
5-OCF3
Ph(2-Cl)

5-116
Me
Me
H
5-OCF3
Ph(2-Me)

5-117
Me
Me
H
5-OCF3
Ph(2-CF3)

5-118
Me
Me
H
5-OCF3
Ph(2-F-6-Cl)

5-119
Me
Me
H
3-OCHF2
Ph(2-F)

5-120
Me
Me
H
3-OCHF2
Ph(2,6-F2)

5-121
Me
Me
H
3-OCHF2
Ph(2-Cl)

5-122
Me
Me
H
3-OCHF2
Ph(2-Me)

5-123
Me
Me
H
3-OCHF2
Ph(2-CF3)

5-124
Me
Me
H
3-OCHF2
Ph(2-F-6-Cl)

5-125
Me
Me
H
4-OCHF2
Ph(2-F)

5-126
Me
Me
H
4-OCHF2
Ph(2,6-F2)

5-127
Me
Me
H
4-OCHF2
Ph(2-Cl)

5-128
Me
Me
H
4-OCHF2
Ph(2-Me)

5-129
Me
Me
H
4-OCHF2
Ph(2-CF3)

5-130
Me
Me
H
4-OCHF2
Ph(2-F-6-Cl)

5-131
Me
Me
H
5-OCHF2
Ph(2-F)

5-132
Me
Me
H
5-OCHF2
Ph(2,6-F2)

5-133
Me
Me
H
5-OCHF2
Ph(2-Cl)

5-134
Me
Me
H
5-OCHF2
Ph(2-Me)

5-135
Me
Me
H
5-OCHF2
Ph(2-CF3)

5-136
Me
Me
H
5-OCHF2
Ph(2-F-6-Cl)

5-137
Me
Me
H
3-OCH2CF3
Ph(2-F)

5-138
Me
Me
H
3-OCH2CF3
Ph(2,6-F2)

5-139
Me
Me
H
3-OCH2CF3
Ph(2-Cl)

5-140
Me
Me
H
3-OCH2CF3
Ph(2-Me)

5-141
Me
Me
H
3-OCH2CF3
Ph(2-CF3)

5-142
Me
Me
H
3-OCH2CF3
Ph(2-F-6-Cl)

5-143
Me
Me
H
4-OCH2CF3
Ph(2-F)

5-144
Me
Me
H
4-OCH2CF3
Ph(2,6-F2)

5-145
Me
Me
H
4-OCH2CF3
Ph(2-Cl)

5-146
Me
Me
H
4-OCH2CF3
Ph(2-Me)

5-147
Me
Me
H
4-OCH2CF3
Ph(2-CF3)

5-148
Me
Me
H
4-OCH2CF3
Ph(2-F-6-Cl)

5-149
Me
Me
H
5-OCH2CF3
Ph(2-F)

5-150
Me
Me
H
5-OCH2CF3
Ph(2,6-F2)

5-151
Me
Me
H
5-OCH2CF3
Ph(2-Cl)

5-152
Me
Me
H
5-OCH2CF3
Ph(2-Me)

5-153
Me
Me
H
5-OCH2CF3
Ph(2-CF3)

5-154
Me
Me
H
5-OCH2CF3
Ph(2-F-6-Cl)

5-155
Me
Me
H
5-Cl
4-trifluoromethyl-3-pyridyl
179-182

5-156
Me
Me
H
4,5-Br2
Ph(2,6-F2)
128-130

5-157
Me
Me
H
4,5-Br2
Ph(2-F)
173-175

5-158
Me
Me
H
3-Me-4-Cl
Ph(2-F)

5-159
Me
Me
H
3-Me-4-Cl
Ph(2,6-F2)

5-160
Me
Me
H
3-Me-4-Cl
Ph(2-Cl)

5-161
Me
Me
H
3-Me-4-Cl
Ph(2-Me)

5-162
Me
Me
H
3-Me-4-Cl
Ph(2-CF3)

5-163
Me
Me
H
3-Me-4-Cl
Ph(2-F-6-Cl)

5-164
Me
Me
H
3-Me-5-Cl
Ph(2-F)

5-165
Me
Me
H
3-Me-5-Cl
Ph(2,6-F2)

5-166
Me
Me
H
3-Me-5-Cl
Ph(2-Cl)

5-167
Me
Me
H
3-Me-5-Cl
Ph(2-Me)

5-168
Me
Me
H
3-Me-5-Cl
Ph(2-CF3)

5-169
Me
Me
H
3-Me-5-Cl
Ph(2-F-6-Cl)

5-170
Me
Me
H
3-Me-4-Br
Ph(2-F)

5-171
Me
Me
H
3-Me-4-Br
Ph(2,6-F2)

5-172
Me
Me
H
3-Me-4-Br
Ph(2-Cl)

5-173
Me
Me
H
3-Me-4-Br
Ph(2-Me)

5-174
Me
Me
H
3-Me-4-Br
Ph(2-CF3)

5-175
Me
Me
H
3-Me-4-Br
Ph(2-F-6-Cl)

5-176
Me
Me
H
3-Me-5-Br
Ph(2-F)

5-177
Me
Me
H
3-Me-5-Br
Ph(2,6-F2)

5-178
Me
Me
H
3-Me-5-Br
Ph(2-Cl)

5-179
Me
Me
H
3-Me-5-Br
Ph(2-Me)

5-180
Me
Me
H
3-Me-5-Br
Ph(2-CF3)

5-181
Me
Me
H
3-Me-5-Br
Ph(2-F-6-Cl)

5-182
Me
Me
H
3-Me-4-CF3
Ph(2-F)

5-183
Me
Me
H
3-Me-4-CF3
Ph(2,6-F2)

5-184
Me
Me
H
3-Me-4-CF3
Ph(2-Cl)

5-185
Me
Me
H
3-Me-4-CF3
Ph(2-Me)

5-186
Me
Me
H
3-Me-4-CF3
Ph(2-CF3)

5-187
Me
Me
H
3-Me-4-CF3
Ph(2-F-6-Cl)

5-188
Me
Me
H
3-Me-5-CF3
Ph(2-F)

5-189
Me
Me
H
3-Me-5-CF3
Ph(2,6-F2)

5-190
Me
Me
H
3-Me-5-CF3
Ph(2-Cl)

5-191
Me
Me
H
3-Me-5-CF3
Ph(2-Me)

5-192
Me
Me
H
3-Me-5-CF3
Ph(2-CF3)

5-193
Me
Me
H
3-Me-5-CF3
Ph(2-F-6-Cl)

5-194
Me
Me
H
3-Me-4-OCF3
Ph(2-F)

5-195
Me
Me
H
3-Me-4-OCF3
Ph(2,6-F2)

5-196
Me
Me
H
3-Me-4-OCF3
Ph(2-Cl)

5-197
Me
Me
H
3-Me-4-OCF3
Ph(2-Me)

5-198
Me
Me
H
3-Me-4-OCF3
Ph(2-CF3)

5-199
Me
Me
H
3-Me-4-OCF3
Ph(2-F-6-Cl)

5-200
Me
Me
H
3-Me-5-OCF3
Ph(2-F)

5-201
Me
Me
H
3-Me-5-OCF3
Ph(2,6-F2)

5-202
Me
Me
H
3-Me-5-OCF3
Ph(2-Cl)

5-203
Me
Me
H
3-Me-5-OCF3
Ph(2-Me)

5-204
Me
Me
H
3-Me-5-OCF3
Ph(2-CF3)

5-205
Me
Me
H
3-Me-5-OCF3
Ph(2-F-6-Cl)

5-206
Me
Me
H
3-Me-4-OCHF2
Ph(2-F)

5-207
Me
Me
H
3-Me-4-OCHF2
Ph(2,6-F2)

5-208
Me
Me
H
3-Me-4-OCHF2
Ph(2-Cl)

5-209
Me
Me
H
3-Me-4-OCHF2
Ph(2-Me)

5-210
Me
Me
H
3-Me-4-OCHF2
Ph(2-CF3)

5-211
Me
Me
H
3-Me-4-OCHF2
Ph(2-F-6-Cl)

5-212
Me
Me
H
3-Me-5-OCHF2
Ph(2-F)

5-213
Me
Me
H
3-Me-5-OCHF2
Ph(2,6-F2)

5-214
Me
Me
H
3-Me-5-OCHF2
Ph(2-Cl)

5-215
Me
Me
H
3-Me-5-OCHF2
Ph(2-Me)

5-216
Me
Me
H
3-Me-5-OCHF2
Ph(2-CF3)

5-217
Me
Me
H
3-Me-5-OCHF2
Ph(2-F-6-Cl)

5-218
Me
Me
H
3-Me-4-OCH2CF3
Ph(2-F)

5-219
Me
Me
H
3-Me-4-OCH2CF3
Ph(2,6-F2)

5-220
Me
Me
H
3-Me-4-OCH2CF3
Ph(2-Cl)

5-221
Me
Me
H
3-Me-4-OCH2CF3
Ph(2-Me)

5-222
Me
Me
H
3-Me-4-OCH2CF3
Ph(2-CF3)

5-223
Me
Me
H
3-Me-4-OCH2CF3
Ph(2-F-6-Cl)

5-224
Me
Me
H
3-Me-5-OCH2CF3
Ph(2-F)

5-225
Me
Me
H
3-Me-5-OCH2CF3
Ph(2,6-F2)

5-226
Me
Me
H
3-Me-5-OCH2CF3
Ph(2-Cl)

5-227
Me
Me
H
3-Me-5-OCH2CF3
Ph(2-Me)

5-228
Me
Me
H
3-Me-5-OCH2CF3
Ph(2-CF3)

5-229
Me
Me
H
3-Me-5-OCH2CF3
Ph(2-F-6-Cl)

5-230
Me
Me
H
3,5-Cl2
Ph(2-F)

5-231
Me
Me
H
3,5-Cl2
Ph(2,6-F2)

5-232
Me
Me
H
3,5-Cl2
Ph(2-Cl)

5-233
Me
Me
H
3,5-Cl2
Ph(2-Me)

5-234
Me
Me
H
3,5-Cl2
Ph(2-CF3)

5-235
Me
Me
H
3,5-Cl2
Ph(2-F-6-Cl)

5-236
Me
Me
H
3-Cl-5-Br
Ph(2-F)

5-237
Me
Me
H
3-Cl-5-Br
Ph(2,6-F2)

5-238
Me
Me
H
3-Cl-5-Br
Ph(2-Cl)

5-239
Me
Me
H
3-Cl-5-Br
Ph(2-Me)

5-240
Me
Me
H
3-Cl-5-Br
Ph(2-CF3)

5-241
Me
Me
H
3-Cl-5-Br
Ph(2-F-6-Cl)

5-242
Me
Me
H
3-Cl-5-CF3
Ph(2-F)

5-243
Me
Me
H
3-Cl-5-CF3
Ph(2,6-F2)

5-244
Me
Me
H
3-Cl-5-CF3
Ph(2-Cl)

5-245
Me
Me
H
3-Cl-5-CF3
Ph(2-Me)

5-246
Me
Me
H
3-Cl-5-CF3
Ph(2-CF3)

5-247
Me
Me
H
3-Cl-5-CF3
Ph(2-F-6-Cl)

5-248
Me
Me
H
3-Cl-5-OCF3
Ph(2-F)

5-249
Me
Me
H
3-Cl-5-OCF3
Ph(2,6-F2)

5-250
Me
Me
H
3-Cl-5-OCF3
Ph(2-Cl)

5-251
Me
Me
H
3-Cl-5-OCF3
Ph(2-Me)

5-252
Me
Me
H
3-Cl-5-OCF3
Ph(2-CF3)

5-253
Me
Me
H
3-Cl-5-OCF3
Ph(2-F-6-Cl)

5-254
Me
Me
H
3-Cl-5-OCHF2
Ph(2-F)

5-255
Me
Me
H
3-Cl-5-OCHF2
Ph(2,6-F2)

5-256
Me
Me
H
3-Cl-5-OCHF2
Ph(2-Cl)

5-257
Me
Me
H
3-Cl-5-OCHF2
Ph(2-Me)

5-258
Me
Me
H
3-Cl-5-OCHF2
Ph(2-CF3)

5-259
Me
Me
H
3-Cl-5-OCHF2
Ph(2-F-6-Cl)

5-260
Me
Me
H
3-Cl-5-OCH2CF3
Ph(2-F)

5-261
Me
Me
H
3-Cl-5-OCH2CF3
Ph(2,6-F2)

5-262
Me
Me
H
3-Cl-5-OCH2CF3
Ph(2-Cl)

5-263
Me
Me
H
3-Cl-5-OCH2CF3
Ph(2-Me)

5-264
Me
Me
H
3-Cl-5-OCH2CF3
Ph(2-CF3)

5-265
Me
Me
H
3-Cl-5-OCH2CF3
Ph(2-F-6-Cl)

[0245]

6

TABLE 6

Physical properties

Compound No.
R1
R2
R3
X
B
(mp ° C.)

6-1
Me
Me
H
H
Ph

6-2
Me
Me
H
H
Ph(2-F)

6-3
Me
Me
H
H
Ph(2-Cl)

6-4
Me
Me
H
H
Ph(2-OMe)

6-5
Me
Me
H
H
Ph(2,6-F2)
139-142

6-6
Me
Me
H
H
Ph(2,6-Cl2)

6-7
Me
Me
H
H
Ph(2,6-OMe2)

6-8
Me
Me
H
2-Cl
Ph

6-9
Me
Me
H
2-Cl
Ph(2-F)

6-10
Me
Me
H
2-Cl
Ph(2-Cl)

6-11
Me
Me
H
2-Cl
Ph(2,6-F2)

6-12
Me
Me
H
2-Cl
Ph(2,6-Cl2)

6-13
Me
Me
H
2-Br
Ph

6-14
Me
Me
H
2-Br
Ph(2-F)

6-15
Me
Me
H
2-Br
Ph(2-Cl)

6-16
Me
Me
H
2-Br
Ph(2,6-F2)

6-17
Me
Me
H
2-Br
Ph(2,6-Cl2)

6-18
Me
Me
H
2-CF3
Ph(2,6-F2)

6-19
Me
Me
H
2-CN
Ph(2,6-F2)

6-20
Me
CN
H
H
Ph(2,6-F2)

6-21
Me
CO2Et
H
H
Ph(2,6-F2)

6-22
Me
CN
H
2-Cl
Ph(2,6-F2)

6-23
Me
CO2Et
H
2-Cl
Ph(2,6-F2)

6-24
Me
Et
H
H
Ph(2,6-F2)

6-25
Me
Me
COMe
H
Ph(2,6-F2)

6-26
Me
Me
CH2OMe
H
Ph(2,6-F2)

6-27
Me
Me
H
H
1-naphthyl

6-28
Me
Me
H
H
2-naphthyl

6-29
Me
Me
H
H
2-thienyl

6-30
Me
Me
H
H
3-thienyl

6-31
Me
Me
H
H
2-pyrazinyl

6-32
Me
Me
H
H
2-pyridyl

6-33
Me
Me
H
H
3-pyridyl

6-34
Me
Me
H
H
4-trifluoro-

methyl-3-pyridyl

6-35
Me
Me
H
H
4-pyridyl

6-36
Me
Me
H
H
2-furyl

6-37
Me
Me
H
H
3-furyl

6-38
Me
Me
H
4-Cl
Ph(2-F)

6-39
Me
Me
H
4-Cl
Ph(2,6-F2)

6-40
Me
Me
H
4-Cl
Ph(2-Cl)

6-41
Me
Me
H
4-Cl
Ph(2-Me)

6-42
Me
Me
H
4-Cl
Ph(2-CF3)

6-43
Me
Me
H
4-Cl
Ph(2-F-6-Cl)

6-44
Me
Me
H
5-Cl
Ph(2-F)

6-45
Me
Me
H
5-Cl
Ph(2,6-F2)

6-46
Me
Me
H
5-Cl
Ph(2-Cl)

6-47
Me
Me
H
5-Cl
Ph(2-Me)

6-48
Me
Me
H
5-Cl
Ph(2-CF3)

6-49
Me
Me
H
5-Cl
Ph(2-F-6-Cl)

6-50
Me
Me
H
5-Br
Ph(2-F)

6-51
Me
Me
H
5-Br
Ph(2,6-F2)

6-52
Me
Me
H
5-Br
Ph(2-Cl)

6-53
Me
Me
H
5-Br
Ph(2-Me)

6-54
Me
Me
H
5-Br
Ph(2-CF3)

6-55
Me
Me
H
5-Br
Ph(2-F-6-Cl)

6-56
Me
Me
H
2-Me
Ph(2-F)

6-57
Me
Me
H
2-Me
Ph(2,6-F2)

6-58
Me
Me
H
2-Me
Ph(2-Cl)

6-59
Me
Me
H
2-Me
Ph(2-Me)

6-60
Me
Me
H
2-Me
Ph(2-CF3)

6-61
Me
Me
H
2-Me
Ph(2-F-6-Cl)

6-62
Me
Me
H
4-Me
Ph(2-F)

6-63
Me
Me
H
4-Me
Ph(2,6-F2)

6-64
Me
Me
H
4-Me
Ph(2-Cl)

6-65
Me
Me
H
4-Me
Ph(2-Me)

6-66
Me
Me
H
4-Me
Ph(2-CF3)

6-67
Me
Me
H
4-Me
Ph(2-F-6-Cl)

6-68
Me
Me
H
5-CF3
Ph(2-F)

6-69
Me
Me
H
5-CF3
Ph(2,6-F2)

6-70
Me
Me
H
5-CF3
Ph(2-Cl)

6-71
Me
Me
H
5-CF3
Ph(2-Me)

6-72
Me
Me
H
5-CF3
Ph(2-CF3)

6-73
Me
Me
H
5-CF3
Ph(2-F-6-Cl)

6-74
Me
Me
H
5-OCF3
Ph(2-F)

6-75
Me
Me
H
5-OCF3
Ph(2,6-F2)

6-76
Me
Me
H
5-OCF3
Ph(2-Cl)

6-77
Me
Me
H
5-OCF3
Ph(2-Me)

6-78
Me
Me
H
5-OCF3
Ph(2-CF3)

6-79
Me
Me
H
5-OCF3
Ph(2-F-6-Cl)

6-80
Me
Me
H
5-OCHF2
Ph(2-F)

6-81
Me
Me
H
5-OCHF2
Ph(2,6-F2)

6-82
Me
Me
H
5-OCHF2
Ph(2-Cl)

6-83
Me
Me
H
5-OCHF2
Ph(2-Me)

6-84
Me
Me
H
5-OCHF2
Ph(2-CF3)

6-85
Me
Me
H
5-OCHF2
Ph(2-F-6-Cl)

6-86
Me
Me
H
5-OCH2CF3
Ph(2-F)

6-87
Me
Me
H
5-OCH2CF3
Ph(2,6-F2)

6-88
Me
Me
H
5-OCH2CF3
Ph(2-Cl)

6-89
Me
Me
H
5-OCH2CF3
Ph(2-Me)

6-90
Me
Me
H
5-OCH2CF3
Ph(2-CF3)

6-91
Me
Me
H
5-OCH2CF3
Ph(2-F-6-Cl)

6-92
Me
Me
H
2,5-Cl2
Ph(2-F)

6-93
Me
Me
H
2,5-Cl2
Ph(2,6-F2)

6-94
Me
Me
H
2,5-Cl2
Ph(2-Cl)

6-95
Me
Me
H
2,5-Cl2
Ph(2-Me)

6-96
Me
Me
H
2,5-Cl2
Ph(2-CF3)

6-97
Me
Me
H
2,5-Cl2
Ph(2-F-6-Cl)

6-98
Me
Me
H
4,5-Cl2
Ph(2-F)

6-99
Me
Me
H
4,5-Cl2
Ph(2,6-F2)

6-100
Me
Me
H
4,5-Cl2
Ph(2-Cl)

6-101
Me
Me
H
4,5-Cl2
Ph(2-Me)

6-102
Me
Me
H
4,5-Cl2
Ph(2-CF3)

6-103
Me
Me
H
4,5-Cl2
Ph(2-F-6-Cl)

6-104
Me
Me
H
2-Cl-5-Br
Ph(2-F)

6-105
Me
Me
H
2-Cl-5-Br
Ph(2,6-F2)

6-106
Me
Me
H
2-Cl-5-Br
Ph(2-Cl)

6-107
Me
Me
H
2-Cl-5-Br
Ph(2-Me)

6-108
Me
Me
H
2-Cl-5-Br
Ph(2-CF3)

6-109
Me
Me
H
2-Cl-5-Br
Ph(2-F-6-Cl)

6-110
Me
Me
H
4-Cl-5-Br
Ph(2-F)

6-111
Me
Me
H
4-Cl-5-Br
Ph(2,6-F2)

6-112
Me
Me
H
4-Cl-5-Br
Ph(2-Cl)

6-113
Me
Me
H
4-Cl-5-Br
Ph(2-Me)

6-114
Me
Me
H
4-Cl-5-Br
Ph(2-CF3)

6-115
Me
Me
H
4-Cl-5-Br
Ph(2-F-6-Cl)

6-116
Me
Me
H
2-Cl-5-CF3
Ph(2-F)

6-117
Me
Me
H
2-Cl-5-CF3
Ph(2,6-F2)

6-118
Me
Me
H
2-Cl-5-CF3
Ph(2-Cl)

6-119
Me
Me
H
2-Cl-5-CF3
Ph(2-Me)

6-120
Me
Me
H
2-Cl-5-CF3
Ph(2-CF3)

6-121
Me
Me
H
2-Cl-5-CF3
Ph(2-F-6-Cl)

6-122
Me
Me
H
4-Cl-5-CF3
Ph(2-F)

6-123
Me
Me
H
4-Cl-5-CF3
Ph(2,6-F2)

6-124
Me
Me
H
4-Cl-5-CF3
Ph(2-Cl)

6-125
Me
Me
H
4-Cl-5-CF3
Ph(2-Me)

6-126
Me
Me
H
4-Cl-5-CF3
Ph(2-CF3)

6-127
Me
Me
H
4-Cl-5-CF3
Ph(2-F-6-Cl)

6-128
Me
Me
H
2-Cl-5-OCF3
Ph(2-F)

6-129
Me
Me
H
2-Cl-5-OCF3
Ph(2,6-F2)

6-130
Me
Me
H
2-Cl-5-OCF3
Ph(2-Cl)

6-131
Me
Me
H
2-Cl-5-OCF3
Ph(2-Me)

6-132
Me
Me
H
2-Cl-5-OCF3
Ph(2-CF3)

6-133
Me
Me
H
2-Cl-5-OCF3
Ph(2-F-6-Cl)

6-134
Me
Me
H
4-Cl-5-OCF3
Ph(2-F)

6-135
Me
Me
H
4-Cl-5-OCF3
Ph(2,6-F2)

6-136
Me
Me
H
4-Cl-5-OCF3
Ph(2-Cl)

6-137
Me
Me
H
4-Cl-5-OCF3
Ph(2-Me)

6-138
Me
Me
H
4-Cl-5-OCF3
Ph(2-CF3)

6-139
Me
Me
H
4-Cl-5-OCF3
Ph(2-F-6-Cl)

6-140
Me
Me
H
2-Cl-5-OCHF2
Ph(2-F)

6-141
Me
Me
H
2-Cl-5-OCHF2
Ph(2,6-F2)

6-142
Me
Me
H
2-Cl-5-OCHF2
Ph(2-Cl)

6-143
Me
Me
H
2-Cl-5-OCHF2
Ph(2-Me)

6-144
Me
Me
H
2-Cl-5-OCHF2
Ph(2-CF3)

6-145
Me
Me
H
2-Cl-5-OCHF2
Ph(2-F-6-Cl)

6-146
Me
Me
H
4-Cl-5-OCHF2
Ph(2-F)

6-147
Me
Me
H
4-Cl-5-OCHF2
Ph(2,6-F2)

6-148
Me
Me
H
4-Cl-5-OCHF2
Ph(2-Cl)

6-149
Me
Me
H
4-Cl-5-OCHF2
Ph(2-Me)

6-150
Me
Me
H
4-Cl-5-OCHF2
Ph(2-CF3)

6-151
Me
Me
H
4-Cl-5-OCHF2
Ph(2-F-6-Cl)

6-152
Me
Me
H
2-Cl-5-OCH2CF3
Ph(2-F)

6-153
Me
Me
H
2-Cl-5-OCH2CF3
Ph(2,6-F2)

6-154
Me
Me
H
2-Cl-5-OCH2CF3
Ph(2-Cl)

6-155
Me
Me
H
2-Cl-5-OCH2CF3
Ph(2-Me)

6-156
Me
Me
H
2-Cl-5-OCH2CF3
Ph(2-CF3)

6-157
Me
Me
H
2-Cl-5-OCH2CF3
Ph(2-F-6-Cl)

6-158
Me
Me
H
4-Cl-5-OCH2CF3
Ph(2-F)

6-159
Me
Me
H
4-Cl-5-OCH2CF3
Ph(2,6-F2)

6-160
Me
Me
H
4-Cl-5-OCH2CF3
Ph(2-Cl)

6-161
Me
Me
H
4-Cl-5-OCH2CF3
Ph(2-Me)

6-162
Me
Me
H
4-Cl-5-OCH2CF3
Ph(2-CF3)

6-163
Me
Me
H
4-Cl-5-OCH2CF3
Ph(2-F-6-Cl)

6-164
Me
Me
H
2-Me-5-Cl
Ph(2-F)

6-165
Me
Me
H
2-Me-5-Cl
Ph(2,6-F2)

6-166
Me
Me
H
2-Me-5-Cl
Ph(2-Cl)

6-167
Me
Me
H
2-Me-5-Cl
Ph(2-Me)

6-168
Me
Me
H
2-Me-5-Cl
Ph(2-CF3)

6-169
Me
Me
H
2-Me-5-Cl
Ph(2-F-6-Cl)

6-170
Me
Me
H
4-Me-5-Cl
Ph(2-F)

6-171
Me
Me
H
4-Me-5-Cl
Ph(2,6-F2)

6-172
Me
Me
H
4-Me-5-Cl
Ph(2-Cl)

6-173
Me
Me
H
4-Me-5-Cl
Ph(2-Me)

6-174
Me
Me
H
4-Me-5-Cl
Ph(2-CF3)

6-175
Me
Me
H
4-Me-5-Cl
Ph(2-F-6-Cl)

6-176
Me
Me
H
2-Me-5-Br
Ph(2-F)

6-177
Me
Me
H
2-Me-5-Br
Ph(2,6-F2)

6-178
Me
Me
H
2-Me-5-Br
Ph(2-Cl)

6-179
Me
Me
H
2-Me-5-Br
Ph(2-Me)

6-180
Me
Me
H
2-Me-5-Br
Ph(2-CF3)

6-181
Me
Me
H
2-Me-5-Br
Ph(2-F-6-Cl)

6-182
Me
Me
H
4-Me-5-Br
Ph(2-F)

6-183
Me
Me
H
4-Me-5-Br
Ph(2,6-F2)

6-184
Me
Me
H
4-Me-5-Br
Ph(2-Cl)

6-185
Me
Me
H
4-Me-5-Br
Ph(2-Me)

6-186
Me
Me
H
4-Me-5-Br
Ph(2-CF3)

6-187
Me
Me
H
4-Me-5-Br
Ph(2-F-6-Cl)

6-188
Me
Me
H
2-Me-5-CF3
Ph(2-F)

6-189
Me
Me
H
2-Me-5-CF3
Ph(2,6-F2)

6-190
Me
Me
H
2-Me-5-CF3
Ph(2-Cl)

6-191
Me
Me
H
2-Me-5-CF3
Ph(2-Me)

6-192
Me
Me
H
2-Me-5-CF3
Ph(2-CF3)

6-193
Me
Me
H
2-Me-5-CF3
Ph(2-F-6-Cl)

6-194
Me
Me
H
4-Me-5-CF3
Ph(2-F)

6-195
Me
Me
H
4-Me-5-CF3
Ph(2,6-F2)

6-196
Me
Me
H
4-Me-5-CF3
Ph(2-Cl)

6-197
Me
Me
H
4-Me-5-CF3
Ph(2-Me)

6-198
Me
Me
H
4-Me-5-CF3
Ph(2-CF3)

6-199
Me
Me
H
4-Me-5-CF3
Ph(2-F-6-Cl)

6-200
Me
Me
H
2-Me-5-OCF3
Ph(2-F)

6-201
Me
Me
H
2-Me-5-OCF3
Ph(2,6-F2)

6-202
Me
Me
H
2-Me-5-OCF3
Ph(2-Cl)

6-203
Me
Me
H
2-Me-5-OCF3
Ph(2-Me)

6-204
Me
Me
H
2-Me-5-OCF3
Ph(2-CF3)

6-205
Me
Me
H
2-Me-5-OCF3
Ph(2-F-6-Cl)

6-206
Me
Me
H
4-Me-5-OCF3
Ph(2-F)

6-207
Me
Me
H
4-Me-5-OCF3
Ph(2,6-F2)

6-208
Me
Me
H
4-Me-5-OCF3
Ph(2-Cl)

6-209
Me
Me
H
4-Me-5-OCF3
Ph(2-Me)

6-210
Me
Me
H
4-Me-5-OCF3
Ph(2-CF3)

6-211
Me
Me
H
4-Me-5-OCF3
Ph(2-F-6-Cl)

6-212
Me
Me
H
2-Me-5-OCHF2
Ph(2-F)

6-213
Me
Me
H
2-Me-5-OCHF2
Ph(2,6-F2)

6-214
Me
Me
H
2-Me-5-OCHF2
Ph(2-Cl)

6-215
Me
Me
H
2-Me-5-OCHF2
Ph(2-Me)

6-216
Me
Me
H
2-Me-5-OCHF2
Ph(2-CF3)

6-217
Me
Me
H
2-Me-5-OCHF2
Ph(2-F-6-Cl)

6-218
Me
Me
H
4-Me-5-OCHF2
Ph(2-F)

6-219
Me
Me
H
4-Me-5-OCHF2
Ph(2,6-F2)

6-220
Me
Me
H
4-Me-5-OCHF2
Ph(2-Cl)

6-221
Me
Me
H
4-Me-5-OCHF2
Ph(2-Me)

6-222
Me
Me
H
4-Me-5-OCHF2
Ph(2-CF3)

6-223
Me
Me
H
4-Me-5-OCHF2
Ph(2-F-6-Cl)

6-224
Me
Me
H
2-Me-5-OCH2CF3
Ph(2-F)

6-225
Me
Me
H
2-Me-5-OCH2CF3
Ph(2,6-F2)

6-226
Me
Me
H
2-Me-5-OCH2CF3
Ph(2-Cl)

6-227
Me
Me
H
2-Me-5-OCH2CF3
Ph(2-Me)

6-228
Me
Me
H
2-Me-5-OCH2CF3
Ph(2-CF3)

6-229
Me
Me
H
2-Me-5-OCH2CF3
Ph(2-F-6-Cl)

6-230
Me
Me
H
4-Me-5-OCH2CF3
Ph(2-F)

6-231
Me
Me
H
4-Me-5-OCH2CF3
Ph(2,6-F2)

6-232
Me
Me
H
4-Me-5-OCH2CF3
Ph(2-Cl)

6-233
Me
Me
H
4-Me-5-OCH2CF3
Ph(2-Me)

6-234
Me
Me
H
4-Me-5-OCH2CF3
Ph(2-CF3)

6-235
Me
Me
H
4-Me-5-OCH2CF3
Ph(2-F-6-Cl)

[0246]

7

TABLE 7

Physical properties

Compound No.
R1
R2
R3
X1
X2
X3
B
(mp ° C.)

7-1
Me
Me
H
Me
Me
Me
Ph(2-Cl)

7-2
Me
Me
H
Me
Me
Me
Ph(4-Cl)

7-3
Me
Me
H
Me
Me
Me
Ph(2-CF3)

7-4
Me
Me
H
Me
Me
Me
Ph(4-CF3)

7-5
Me
Me
H
Me
Me
Me
Ph(2-F)

7-6
Me
Me
H
Me
Me
Me
Ph(2,6-F2)

7-7
Me
Me
H
Me
Me
Me
Ph(2,6-(OMe)2)

7-8
Me
Me
H
Cl
Cl
Me
Ph(2-Cl)

7-9
Me
Me
H
Cl
Cl
Me
Ph(4-Cl)

7-10
Me
Me
H
Cl
Cl
Me
Ph(2-CF3)

7-11
Me
Me
H
Cl
Cl
Me
Ph(4-CF3)

7-12
Me
Me
H
Cl
Cl
Me
Ph(2-F)

7-13
Me
Me
H
Cl
Cl
Me
Ph(2,6-F2)

7-14
Me
Me
H
Cl
Me
Me
Ph(2-Cl)

7-15
Me
Me
H
Cl
Me
Me
Ph(4-Cl)

7-16
Me
Me
H
Cl
Me
Me
Ph(2-CF3)

7-17
Me
Me
H
Cl
Me
Me
Ph(4-CF3)

7-18
Me
Me
H
Cl
Me
Me
Ph(2-F)

7-19
Me
Me
H
Cl
Me
Me
Ph(2,6-F2)

7-20
Me
Me
H
Cl
CF3
Me
Ph(2-Cl)

7-21
Me
Me
H
Cl
CF3
Me
Ph(4-Cl)

7-22
Me
Me
H
Cl
CF3
Me
Ph(2-CF3)

7-23
Me
Me
H
Cl
CF3
Me
Ph(4-CF3)

7-24
Me
Me
H
Cl
CF3
Me
Ph(2-F)

7-25
Me
Me
H
Cl
CF3
Me
Ph(2,6-F2)

7-26
Me
Me
H
Me
H
Me
Ph(2-F)

7-27
Me
Me
H
Me
H
Me
Ph(2,6-F2)

7-28
Me
Me
H
Me
H
Me
Ph(2-Cl)

7-29
Me
Me
H
Me
H
Me
Ph(2-Me)

7-30
Me
Me
H
Me
H
Me
Ph(2-CF3)

7-31
Me
Me
H
Me
H
Me
Ph(2-F-6-Cl)

7-32
Me
Me
H
H
Me
Me
Ph(2-F)

7-33
Me
Me
H
H
Me
Me
Ph(2,6-F2)

7-34
Me
Me
H
H
Me
Me
Ph(2-Cl)

7-35
Me
Me
H
H
Me
Me
Ph(2-Me)

7-36
Me
Me
H
H
Me
Me
Ph(2-CF3)

7-37
Me
Me
H
H
Me
Me
Ph(2-F-6-Cl)

7-38
Me
Me
H
H
H
H
Ph(2-F)

7-39
Me
Me
H
H
H
H
Ph(2,6-F2)

7-40
Me
Me
H
H
H
H
Ph(2-Cl)

7-41
Me
Me
H
H
H
H
Ph(2-Me)

7-42
Me
Me
H
H
H
H
Ph(2-CF3)

7-43
Me
Me
H
H
H
H
Ph(2-F-6-Cl)

7-44
Me
Me
H
Me
H
H
Ph(2-F)

7-45
Me
Me
H
Me
H
H
Ph(2,6-F2)

7-46
Me
Me
H
Me
H
H
Ph(2-Cl)

7-47
Me
Me
H
Me
H
H
Ph(2-Me)

7-48
Me
Me
H
Me
H
H
Ph(2-CF3)

7-49
Me
Me
H
Me
H
H
Ph(2-F-6-Cl)

7-50
Me
Me
H
Cl
H
H
Ph(2-F)

7-51
Me
Me
H
Cl
H
H
Ph(2,6-F2)

7-52
Me
Me
H
Cl
H
H
Ph(2-Cl)

7-53
Me
Me
H
Cl
H
H
Ph(2-Me)

7-54
Me
Me
H
Cl
H
H
Ph(2-CF3)

7-55
Me
Me
H
Cl
H
H
Ph(2-F-6-Cl)

7-56
Me
Me
H
H
Me
H
Ph(2-F)

7-57
Me
Me
H
H
Me
H
Ph(2,6-F2)

7-58
Me
Me
H
H
Me
H
Ph(2-Cl)

7-59
Me
Me
H
H
Me
H
Ph(2-Me)

7-60
Me
Me
H
H
Me
H
Ph(2-CF3)

7-61
Me
Me
H
H
Me
H
Ph(2-F-6-Cl)

7-62
Me
Me
H
H
Cl
H
Ph(2-F)

7-63
Me
Me
H
H
Cl
H
Ph(2,6-F2)

7-64
Me
Me
H
H
Cl
H
Ph(2-Cl)

7-65
Me
Me
H
H
Cl
H
Ph(2-Me)

7-66
Me
Me
H
H
Cl
H
Ph(2-CF3)

7-67
Me
Me
H
H
Cl
H
Ph(2-F-6-Cl)

7-68
Me
Me
H
H
H
Et
Ph(2-F)

7-69
Me
Me
H
H
H
Et
Ph(2,6-F2)

7-70
Me
Me
H
H
H
Et
Ph(2-Cl)

7-71
Me
Me
H
H
H
Et
Ph(2-Me)

7-72
Me
Me
H
H
H
Et
Ph(2-CF3)

7-73
Me
Me
H
H
H
Et
Ph(2-F-6-Cl)

7-74
Me
Me
H
Me
H
Et
Ph(2-F)

7-75
Me
Me
H
Me
H
Et
Ph(2,6-F2)

7-76
Me
Me
H
Me
H
Et
Ph(2-Cl)

7-77
Me
Me
H
Me
H
Et
Ph(2-Me)

7-78
Me
Me
H
Me
H
Et
Ph(2-CF3)

7-79
Me
Me
H
Me
H
Et
Ph(2-F-6-Cl)

7-80
Me
Me
H
Cl
H
Et
Ph(2-F)

7-81
Me
Me
H
Cl
H
Et
Ph(2,6-F2)

7-82
Me
Me
H
Cl
H
Et
Ph(2-Cl)

7-83
Me
Me
H
Cl
H
Et
Ph(2-Me)

7-84
Me
Me
H
Cl
H
Et
Ph(2-CF3)

7-85
Me
Me
H
Cl
H
Et
Ph(2-F-6-Cl)

7-86
Me
Me
H
H
Me
Et
Ph(2-F)

7-87
Me
Me
H
H
Me
Et
Ph(2,6-F2)

7-88
Me
Me
H
H
Me
Et
Ph(2-Cl)

7-89
Me
Me
H
H
Me
Et
Ph(2-Me)

7-90
Me
Me
H
H
Me
Et
Ph(2-CF3)

7-91
Me
Me
H
H
Me
Et
Ph(2-F-6-Cl)

7-92
Me
Me
H
H
Cl
Et
Ph(2-F)

7-93
Me
Me
H
H
Cl
Et
Ph(2,6-F2)

7-94
Me
Me
H
H
Cl
Et
Ph(2-Cl)

7-95
Me
Me
H
H
Cl
Et
Ph(2-Me)

7-96
Me
Me
H
H
Cl
Et
Ph(2-CF3)

7-97
Me
Me
H
H
Cl
Et
Ph(2-F-6-Cl)

7-98
Me
Me
H
H
H
Ph
Ph(2-F)

7-99
Me
Me
H
H
H
Ph
Ph(2,6-F2)

7-100
Me
Me
H
H
H
Ph
Ph(2-Cl)

7-101
Me
Me
H
H
H
Ph
Ph(2-Me)

7-102
Me
Me
H
H
H
Ph
Ph(2-CF3)

7-103
Me
Me
H
H
H
Ph
Ph(2-F-6-Cl)

7-104
Me
Me
H
Me
H
Ph
Ph(2-F)

7-105
Me
Me
H
Me
H
Ph
Ph(2,6-F2)

7-106
Me
Me
H
Me
H
Ph
Ph(2-Cl)

7-107
Me
Me
H
Me
H
Ph
Ph(2-Me)

7-108
Me
Me
H
Me
H
Ph
Ph(2-CF3)

7-109
Me
Me
H
Me
H
Ph
Ph(2-F-6-Cl)

7-110
Me
Me
H
Cl
H
Ph
Ph(2-F)

7-111
Me
Me
H
Cl
H
Ph
Ph(2,6-F2)

7-112
Me
Me
H
Cl
H
Ph
Ph(2-Cl)

7-113
Me
Me
H
Cl
H
Ph
Ph(2-Me)

7-114
Me
Me
H
Cl
H
Ph
Ph(2-CF3)

7-115
Me
Me
H
Cl
H
Ph
Ph(2-F-6-Cl)

7-116
Me
Me
H
H
Me
Ph
Ph(2-F)

7-117
Me
Me
H
H
Me
Ph
Ph(2,6-F2)

7-118
Me
Me
H
H
Me
Ph
Ph(2-Cl)

7-119
Me
Me
H
H
Me
Ph
Ph(2-Me)

7-120
Me
Me
H
H
Me
Ph
Ph(2-CF3)

7-121
Me
Me
H
H
Me
Ph
Ph(2-F-6-Cl)

7-122
Me
Me
H
H
Cl
Ph
Ph(2-F)

7-123
Me
Me
H
H
Cl
Ph
Ph(2-6-F2)

7-124
Me
Me
H
H
Cl
Ph
Ph(2-Cl)

7-125
Me
Me
H
H
Cl
Ph
Ph(2-Me)

7-126
Me
Me
H
H
Cl
Ph
Ph(2-CF3)

7-127
Me
Me
H
H
Cl
Ph
Ph(2-F-6-Cl)

7-128
Me
Me
H
H
H
Ph(4-Cl)
Ph(2-F)

7-129
Me
Me
H
H
H
Ph(4-Cl)
Ph(2,6-F2)

7-130
Me
Me
H
H
H
Ph(4-Cl)
Ph(2-Cl)

7-131
Me
Me
H
H
H
Ph(4-C1)
Ph(2-Me)

7-132
Me
Me
H
H
H
Ph(4-Cl)
Ph(2-CF3)

7-133
Me
Me
H
H
H
Ph(4-Cl)
Ph(2-F-6-Cl)

7-134
Me
Me
H
Me
H
Ph(4-Cl)
Ph(2-F)

7-135
Me
Me
H
Me
H
Ph(4-Cl)
Ph(2,6-F2)

7-136
Me
Me
H
Me
H
Ph(4-Cl)
Ph(2-Cl)

7-137
Me
Me
H
Me
H
Ph(4-Cl)
Ph(2-Me)

7-138
Me
Me
H
Me
H
Ph(4-Cl)
Ph(2-CF3)

7-139
Me
Me
H
Me
H
Ph(4-Cl)
Ph(2-F-6-Cl)

7-140
Me
Me
H
Cl
H
Ph(4-Cl)
Ph(2-F)

7-141
Me
Me
H
Cl
H
Ph(4-Cl)
Ph(2,6-F2)

7-142
Me
Me
H
Cl
H
Ph(4-Cl)
Ph(2-Cl)

7-143
Me
Me
H
Cl
H
Ph(4-Cl)
Ph(2-Me)

7-144
Me
Me
H
Cl
H
Ph(4-Cl)
Ph(2-CF3)

7-145
Me
Me
H
Cl
H
Ph(4-Cl)
Ph(2-F-6-Cl)

7-146
Me
Me
H
H
Me
Ph(4-Cl)
Ph(2-F)

7-147
Me
Me
H
H
Me
Ph(4-Cl)
Ph(2,6-F2)

7-148
Me
Me
H
H
Me
Ph(4-Cl)
Ph(2-Cl)

7-149
Me
Me
H
H
Me
Ph(4-Cl)
Ph(2-Me)

7-150
Me
Me
H
H
Me
Ph(4-Cl)
Ph(2-CF3)

7-151
Me
Me
H
H
Me
Ph(4-Cl)
Ph(2-F-6-Cl)

7-152
Me
Me
H
H
Cl
Ph(4-Cl)
Ph(2-F)

7-153
Me
Me
H
H
Cl
Ph(4-Cl)
Ph(2,6-F2)

7-154
Me
Me
H
H
Cl
Ph(4-Cl)
Ph(2-Cl)

7-155
Me
Me
H
H
Cl
Ph(4-Cl)
Ph(2-Me)

7-156
Me
Me
H
H
Cl
Ph(4-Cl)
Ph(2-CF3)

7-157
Me
Me
H
H
Cl
Ph(4-Cl)
Ph(2-F-6-Cl)

7-158
Me
Me
H
H
H
Ph(4-CF3)
Ph(2-F)

7-159
Me
Me
H
H
H
Ph(4-CF3)
Ph(2,6-F2)

7-160
Me
Me
H
H
H
Ph(4-CF3)
Ph(2-Cl)

7-161
Me
Me
H
H
H
Ph(4-CF3)
Ph(2-Me)

7-162
Me
Me
H
H
H
Ph(4-CF3)
Ph(2-CF3)

7-163
Me
Me
H
H
H
Ph(4-CF3)
Ph(2-F-6-Cl)

7-164
Me
Me
H
Me
H
Ph(4-CF3)
Ph(2-F)

7-165
Me
Me
H
Me
H
Ph(4-CF3)
Ph(2,6-F2)

7-166
Me
Me
H
Me
H
Ph(4-CF3)
Ph(2-Cl)

7-167
Me
Me
H
Me
H
Ph(4-CF3)
Ph(2-Me)

7-168
Me
Me
H
Me
H
Ph(4-CF3)
Ph(2-CF3)

7-169
Me
Me
H
Me
H
Ph(4-CF3)
Ph(2-F-6-Cl)

7-170
Me
Me
H
Cl
H
Ph(4-CF3)
Ph(2-F)

7-171
Me
Me
H
Cl
H
Ph(4-CF3)
Ph(2,6-F2)

7-172
Me
Me
H
Cl
H
Ph(4-CF3)
Ph(2-Cl)

7-173
Me
Me
H
Cl
H
Ph(4-CF3)
Ph(2-Me)

7-174
Me
Me
H
Cl
H
Ph(4-CF3)
Ph(2-CF3)

7-175
Me
Me
H
Cl
H
Ph(4-CF3)
Ph(2-F-6-Cl)

7-176
Me
Me
H
H
Me
Ph(4-CF3)
Ph(2-F)

7-177
Me
Me
H
H
Me
Ph(4-CF3)
Ph(2,6-F2)

7-178
Me
Me
H
H
Me
Ph(4-CF3)
Ph(2-Cl)

7-179
Me
Me
H
H
Me
Ph(4-CF3)
Ph(2-Me)

7-180
Me
Me
H
H
Me
Ph(4-CF3)
Ph(2-CF3)

7-181
Me
Me
H
H
Me
Ph(4-CF3)
Ph(2-F-6-Cl)

7-182
Me
Me
H
H
Cl
Ph(4-CF3)
Ph(2-F)

7-183
Me
Me
H
H
Cl
Ph(4-CF3)
Ph(2,6-F2)

7-184
Me
Me
H
H
Cl
Ph(4-CF3)
Ph(2-Cl)

7-185
Me
Me
H
H
Cl
Ph(4-CF3)
Ph(2-Me)

7-186
Me
Me
H
H
Cl
Ph(4-CF3)
Ph(2-CF3)

7-187
Me
Me
H
H
Cl
Ph(4-CF3)
Ph(2-F-6-Cl)

[0247]

8

TABLE 8

Physical properties

Compound No.
R1
R2
R3
X
B
(mp ° C.)

8-1
Me
Me
H
H
Ph

8-2
Me
Me
H
H
Ph(2-F)
44-45

8-3
Me
Me
H
H
Ph(2-Cl)

8-4
Me
Me
H
H
Ph(2-OMe)

8-5
Me
Me
H
H
Ph(2,6-F2)
112-114

8-6
Me
Me
H
H
Ph(2,6-Cl2)

8-7
Me
Me
H
H
Ph(2,6-OMe2)

8-8
Me
Me
H
6-Cl
Ph

8-9
Me
Me
H
6-Cl
Ph(2-F)

8-10
Me
Me
H
6-Cl
Ph(2-Cl)

8-11
Me
Me
H
6-Cl
Ph(2,6-F2)

8-12
Me
Me
H
6-Cl
Ph(2,6-Cl2)

8-13
Me
Me
H
6-Br
Ph

8-14
Me
Me
H
6-Br
Ph(2-F)

8-15
Me
Me
H
6-Br
Ph(2-Cl)

8-16
Me
Me
H
6-Br
Ph(2,6-F2)

8-17
Me
Me
H
6-Br
Ph(2,6-Cl2)

8-18
Me
Me
H
6-CF3
Ph(2,6-F2)

8-19
Me
Me
H
6-CN
Ph(2,6-F2)

8-20
Me
CN
H
H
Ph(2,6-F2)

8-21
Me
CO2Et
H
H
Ph(2,6-F2)

8-22
Me
CN
H
6-Cl
Ph(2,6-F2)

8-23
Me
CO2Et
H
6-Cl
Ph(2,6-F2)

8-24
Me
Et
H
H
Ph(2,6-F2)

8-25
Me
Me
COMe
H
Ph(2,6-F2)

8-26
Me
Me
CH2OMe
H
Ph(2,6-F2)

8-27
Me
Me
H
H
1-naphthyl

8-28
Me
Me
H
H
2-naphthyl

8-29
Me
Me
H
H
2-thienyl

8-30
Me
Me
H
H
3-thienyl

8-31
Me
Me
H
H
2-pyrazinyl

8-32
Me
Me
H
H
2-pyridyl

8-33
Me
Me
H
H
3-pyridyl

8-34
Me
Me
H
H
4-trifluoromethyl-3-pyridyl

8-35
Me
Me
H
H
4-pyridyl

8-36
Me
Me
H
H
2-furyl

8-37
Me
Me
H
H
3-furyl

8-38
Me
Me
H
5-Cl
Ph(2-F)

8-39
Me
Me
H
5-Cl
Ph(2,6-F2)

8-40
Me
Me
H
5-Br
Ph(2-F)

8-41
Me
Me
H
5-Br
Ph(2,6-F2)

8-42
Me
Me
H
5-CF3
Ph(2-F)

8-43
Me
Me
H
5-CF3
Ph(2,6-F2)
116-119

8-44
Me
Me
H
5-OSO2CF3
Ph(2-F)

8-45
Me
Me
H
5-OSO2CF3
Ph(2,6-F2)

8-46
Me
Me
H
5-OCH2CF3
Ph(2-F)

8-47
Me
Me
H
5-OCH2CF3
Ph(2,6-F2)

8-48
Me
Me
H
3-Cl
Ph(2-F)

8-49
Me
Me
H
3-Cl
Ph(2,6-F2)

8-50
Me
Me
H
3-Cl
Ph(2-Cl)

8-51
Me
Me
H
3-Cl
Ph(2-Me)

8-52
Me
Me
H
3-Cl
Ph(2-CF3)

8-53
Me
Me
H
3-Cl
Ph(2-F-6-Cl)

8-54
Me
Me
H
3-Me
Ph(2-F)

8-55
Me
Me
H
3-Me
Ph(2,6-F2)

8-56
Me
Me
H
3-Me
Ph(2-Cl)

8-57
Me
Me
H
3-Me
Ph(2-Me)

8-58
Me
Me
H
3-Me
Ph(2-CF3)

8-59
Me
Me
H
3-Me
Ph(2-F-6-Cl)

8-60
Me
Me
H
5-Me
Ph(2-F)

8-61
Me
Me
H
5-Me
Ph(2,6-F2)

8-62
Me
Me
H
5-Me
Ph(2-Cl)

8-63
Me
Me
H
5-Me
Ph(2-Me)

8-64
Me
Me
H
5-Me
Ph(2-CF3)

8-65
Me
Me
H
5-Me
Ph(2-F-6-Cl)

8-66
Me
Me
H
6-Me
Ph(2-F)

8-67
Me
Me
H
6-Me
Ph(2,6-F2)

8-68
Me
Me
H
6-Me
Ph(2-Cl)

8-69
Me
Me
H
6-Me
Ph(2-Me)

8-70
Me
Me
H
6-Me
Ph(2-CF3)

8-71
Me
Me
H
6-Me
Ph(2-F-6-Cl)

8-72
Me
Me
H
5-OCF3
Ph(2-F)

8-73
Me
Me
H
5-OCF3
Ph(2,6-F2)

8-74
Me
Me
H
5-OCF3
Ph(2-Cl)

8-75
Me
Me
H
5-OCF3
Ph(2-Me)

8-76
Me
Me
H
5-OCF3
Ph(2-CF3)

8-77
Me
Me
H
5-OCF3
Ph(2-F-6-Cl)

8-78
Me
Me
H
6-OCF3
Ph(2-F)

8-79
Me
Me
H
6-OCF3
Ph(2,6-F2)

8-80
Me
Me
H
6-OCF3
Ph(2-Cl)

8-81
Me
Me
H
6-OCF3
Ph(2-Me)

8-82
Me
Me
H
6-OCF3
Ph(2-CF3)

8-83
Me
Me
H
6-OCF3
Ph(2-F-6-Cl)

8-84
Me
Me
H
5-OCHF2
Ph(2-F)

8-85
Me
Me
H
5-OCHF2
Ph(2,6-F2)

8-86
Me
Me
H
5-OCHF2
Ph(2-Cl)

8-87
Me
Me
H
5-OCHF2
Ph(2-Me)

8-88
Me
Me
H
5-OCHF2
Ph(2-CF3)

8-89
Me
Me
H
5-OCHF2
Ph(2-F-6-Cl)

8-90
Me
Me
H
6-OCHF2
Ph(2-F)

8-91
Me
Me
H
6-OCHF2
Ph(2,6-F2)

8-92
Me
Me
H
6-OCHF2
Ph(2-Cl)

8-93
Me
Me
H
6-OCHF2
Ph(2-Me)

8-94
Me
Me
H
6-OCHF2
Ph(2-CF3)

8-95
Me
Me
H
6-OCHF2
Ph(2-F-6-Cl)

8-96
Me
Me
H
3,5-Cl2
Ph(2-F)

8-97
Me
Me
H
3,5-Cl2
Ph(2,6-F2)

8-98
Me
Me
H
3,5-Cl2
Ph(2-Cl)

8-99
Me
Me
H
3,5-Cl2
Ph(2-Me)

8-100
Me
Me
H
3,5-Cl2
Ph(2-CF3)

8-101
Me
Me
H
3,5-Cl2
Ph(2-F-6-Cl)

8-102
Me
Me
H
4,5-Cl2
Ph(2-F)

8-103
Me
Me
H
4,5-Cl2
Ph(2,6-F2)

8-104
Me
Me
H
4,5-Cl2
Ph(2-Cl)

8-105
Me
Me
H
4,5-Cl2
Ph(2-Me)

8-106
Me
Me
H
4,5-Cl2
Ph(2-CF3)

8-107
Me
Me
H
4,5-Cl2
Ph(2-F-6-Cl)

8-108
Me
Me
H
3-Cl-5-Br
Ph(2-F)

8-109
Me
Me
H
3-Cl-5-Br
Ph(2,6-F2)

8-110
Me
Me
H
3-Cl-5-Br
Ph(2-Cl)

8-111
Me
Me
H
3-Cl-5-Br
Ph(2-Me)

8-112
Me
Me
H
3-Cl-5-Br
Ph(2-CF3)

8-113
Me
Me
H
3-Cl-5-Br
Ph(2-F-6-Cl)

8-114
Me
Me
H
4-Cl-5-Br
Ph(2-F)

8-115
Me
Me
H
4-Cl-5-Br
Ph(2,6-F2)

8-116
Me
Me
H
4-Cl-5-Br
Ph(2-Cl)

8-117
Me
Me
H
4-Cl-5-Br
Ph(2-Me)

8-118
Me
Me
H
4-Cl-5-Br
Ph(2-CF3)

8-119
Me
Me
H
4-Cl-5-Br
Ph(2-F-6-Cl)

8-120
Me
Me
H
3-Cl-5-CF3
Ph(2-F)

8-121
Me
Me
H
3-Cl-5-CF3
Ph(2,6-F2)
159-162

8-122
Me
Me
H
3-Cl-5-CF3
Ph(2-Cl)

8-123
Me
Me
H
3-Cl-5-CF3
Ph(2-Me)

8-124
Me
Me
H
3-Cl-5-CF3
Ph(2-CF3)

8-125
Me
Me
H
3-Cl-5-CF3
Ph(2-F-6-Cl)

8-126
Me
Me
H
4-Cl-5-CF3
Ph(2-F)

8-127
Me
Me
H
4-Cl-5-CF3
Ph(2,6-F2)

8-128
Me
Me
H
4-Cl-5-CF3
Ph(2-Cl)

8-129
Me
Me
H
4-Cl-5-CF3
Ph(2-Me)

8-130
Me
Me
H
4-Cl-5-CF3
Ph(2-CF3)

8-131
Me
Me
H
4-Cl-5-CF3
Ph(2-F-6-Cl)

8-132
Me
Me
H
3-Cl-5-OCF3
Ph(2-F)

8-133
Me
Me
H
3-Cl-5-OCF3
Ph(2,6-F2)

8-134
Me
Me
H
3-Cl-5-OCF3
Ph(2-Cl)

8-135
Me
Me
H
3-Cl-5-OCF3
Ph(2-Me)

8-136
Me
Me
H
3-Cl-5-OCF3
Ph(2-CF3)

8-137
Me
Me
H
3-Cl-5-OCF3
Ph(2-F-6-Cl)

8-138
Me
Me
H
4-Cl-5-OCF3
Ph(2-F)

8-139
Me
Me
H
4-Cl-5-OCF3
Ph(2,6-F2)

8-140
Me
Me
H
4-Cl-5-OCF3
Ph(2-Cl)

8-141
Me
Me
H
4-Cl-5-OCF3
Ph(2-Me)

8-142
Me
Me
H
4-Cl-5-OCF3
Ph(2-CF3)

8-143
Me
Me
H
4-Cl-5-OCF3
Ph(2-F-6-Cl)

8-144
Me
Me
H
3-Cl-5-OCHF2
Ph(2-F)

8-145
Me
Me
H
3-Cl-5-OCHF2
Ph(2,6-F2)

8-146
Me
Me
H
3-Cl-5-OCHF2
Ph(2-Cl)

8-147
Me
Me
H
3-Cl-5-OCHF2
Ph(2-Me)

8-148
Me
Me
H
3-Cl-5-OCHF2
Ph(2-CF3)

8-149
Me
Me
H
3-Cl-5-OCHF2
Ph(2-F-6-Cl)

8-150
Me
Me
H
4-Cl-5-OCHF2
Ph(2-F)

8-151
Me
Me
H
4-Cl-5-OCHF2
Ph(2,6-F2)

8-152
Me
Me
H
4-Cl-5-OCHF2
Ph(2-Cl)

8-153
Me
Me
H
4-Cl-5-OCHF2
Ph(2-Me)

8-154
Me
Me
H
4-Cl-5-OCHF2
Ph(2-CF3)

8-155
Me
Me
H
4-Cl-5-OCHF2
Ph(2-F-6-Cl)

8-156
Me
Me
H
3-Cl-5-OCH2CF3
Ph(2-F)

8-157
Me
Me
H
3-Cl-5-OCH2CF3
Ph(2,6-F2)

8-158
Me
Me
H
3-Cl-5-OCH2CF3
Ph(2-Cl)

8-159
Me
Me
H
3-Cl-5-OCH2CF3
Ph(2-Me)

8-160
Me
Me
H
3-Cl-5-OCH2CF3
Ph(2-CF3)

8-161
Me
Me
H
3-Cl-5-OCH2CF3
Ph(2-F-6-Cl)

8-162
Me
Me
H
4-Cl-5-OCH2CF3
Ph(2-F)

8-163
Me
Me
H
4-Cl-5-OCH2CF3
Ph(2,6-F2)

8-164
Me
Me
H
4-Cl-5-OCH2CF3
Ph(2-Cl)

8-165
Me
Me
H
4-Cl-5-OCH2CF3
Ph(2-Me)

8-166
Me
Me
H
4-Cl-5-OCH2CF3
Ph(2-CF3)

8-167
Me
Me
H
4-Cl-5-OCH2CF3
Ph(2-F-6-Cl)

8-168
Me
Me
H
3-Me-5-Cl
Ph(2-F)

8-169
Me
Me
H
3-Me-5-Cl
Ph(2,6-F2)

8-170
Me
Me
H
3-Me-5-Cl
Ph(2-Cl)

8-171
Me
Me
H
3-Me-5-Cl
Ph(2-Me)

8-172
Me
Me
H
3-Me-5-Cl
Ph(2-CF3)

8-173
Me
Me
H
3-Me-5-Cl
Ph(2-F-6-Cl)

8-174
Me
Me
H
4-Me-5-Cl
Ph(2-F)

8-175
Me
Me
H
4-Me-5-Cl
Ph(2,6-F2)

8-176
Me
Me
H
4-Me-5-Cl
Ph(2-Cl)

8-177
Me
Me
H
4-Me-5-Cl
Ph(2-Me)

8-178
Me
Me
H
4-Me-5-Cl
Ph(2-CF3)

8-179
Me
Me
H
4-Me-5-Cl
Ph(2-F-6-Cl)

8-180
Me
Me
H
3-Me-5-Br
Ph(2-F)

8-181
Me
Me
H
3-Me-5-Br
Ph(2,6-F2)

8-182
Me
Me
H
3-Me-5-Br
Ph(2-Cl)

8-183
Me
Me
H
3-Me-5-Br
Ph(2-Me)

8-184
Me
Me
H
3-Me-5-Br
Ph(2-CF3)

8-185
Me
Me
H
3-Me-5-Br
Ph(2-F-6-Cl)

8-186
Me
Me
H
4-Me-5-Br
Ph(2-F)

8-187
Me
Me
H
4-Me-5-Br
Ph(2,6-F2)

8-188
Me
Me
H
4-Me-5-Br
Ph(2-Cl)

8-189
Me
Me
H
4-Me-5-Br
Ph(2-Me)

8-190
Me
Me
H
4-Me-5-Br
Ph(2-CF3)

8-191
Me
Me
H
4-Me-5-Br
Ph(2-F-6-Cl)

8-192
Me
Me
H
3-Me-5-CF3
Ph(2-F)

8-193
Me
Me
H
3-Me-5-CF3
Ph(2,6-F2)

8-194
Me
Me
H
3-Me-5-CF3
Ph(2-Cl)

8-195
Me
Me
H
3-Me-5-CF3
Ph(2-Me)

8-196
Me
Me
H
3-Me-5-CF3
Ph(2-CF3)

8-197
Me
Me
H
3-Me-5-CF3
Ph(2-F-6-Cl)

8-198
Me
Me
H
4-Me-5-CF3
Ph(2-F)

8-199
Me
Me
H
4-Me-5-CF3
Ph(2,6-F2)

8-200
Me
Me
H
4-Me-5-CF3
Ph(2-Cl)

8-201
Me
Me
H
4-Me-5-CF3
Ph(2-Me)

8-202
Me
Me
H
4-Me-5-CF3
Ph(2-CF3)

8-203
Me
Me
H
4-Me-5-CF3
Ph(2-F-6-Cl)

8-204
Me
Me
H
3-Me-5-OCF3
Ph(2-F)

8-205
Me
Me
H
3-Me-5-OCF3
Ph(2,6-F2)

8-206
Me
Me
H
3-Me-5-OCF3
Ph(2-Cl)

8-207
Me
Me
H
3-Me-5-OCF3
Ph(2-Me)

8-208
Me
Me
H
3-Me-5-OCF3
Ph(2-CF3)

8-209
Me
Me
H
3-Me-5-OCF3
Ph(2-F-6-Cl)

8-210
Me
Me
H
4-Me-5-OCF3
Ph(2-F)

8-211
Me
Me
H
4-Me-5-OCF3
Ph(2,6-F2)

8-212
Me
Me
H
4-Me-5-OCF3
Ph(2-Cl)

8-213
Me
Me
H
4-Me-5-OCF3
Ph(2-Me)

8-214
Me
Me
H
4-Me-5-OCF3
Ph(2-CF3)

8-215
Me
Me
H
4-Me-5-OCF3
Ph(2-F-6-Cl)

8-216
Me
Me
H
3-Me-5-OCHF2
Ph(2-F)

8-217
Me
Me
H
3-Me-5-OCHF2
Ph(2,6-F2)

8-218
Me
Me
H
3-Me-5-OCHF2
Ph(2-Cl)

8-219
Me
Me
H
3-Me-5-OCHF2
Ph(2-Me)

8-220
Me
Me
H
3-Me-5-OCHF2
Ph(2-CF3)

8-221
Me
Me
H
3-Me-5-OCHF2
Ph(2-F-6-Cl)

8-222
Me
Me
H
4-Me-5-OCHF2
Ph(2-F)

8-223
Me
Me
H
4-Me-5-OCHF2
Ph(2,6-F2)

8-224
Me
Me
H
4-Me-5-OCHF2
Ph(2-Cl)

8-225
Me
Me
H
4-Me-5-OCHF2
Ph(2-Me)

8-226
Me
Me
H
4-Me-5-OCHF2
Ph(2-CF3)

8-227
Me
Me
H
4-Me-5-OCHF2
Ph(2-F-6-Cl)

8-228
Me
Me
H
3-Me-5-OCH2CF3
Ph(2-F)

8-229
Me
Me
H
3-Me-5-OCH2CF3
Ph(2,6-F2)

8-230
Me
Me
H
3-Me-5-OCH2CF3
Ph(2-Cl)

8-231
Me
Me
H
3-Me-5-OCH2CF3
Ph(2-Me)

8-232
Me
Me
H
3-Me-5-OCH2CF3
Ph(2-CF3)

8-233
Me
Me
H
3-Me-5-OCH2CF3
Ph(2-F-6-Cl)

8-234
Me
Me
H
4-Me-5-OCH2CF3
Ph(2-F)

8-235
Me
Me
H
4-Me-5-OCH2CF3
Ph(2,6-F2)

8-236
Me
Me
H
4-Me-5-OCH2CF3
Ph(2-Cl)

8-237
Me
Me
H
4-Me-5-OCH2CF3
Ph(2-Me)

8-238
Me
Me
H
4-Me-5-OCH2CF3
Ph(2-CF3)

8-239
Me
Me
H
4-Me-5-OCH2CF3
Ph(2-F-6-Cl)

[0248]

9

TABLE 9

Physical

Compound

properties

No.
R1
R2
R3
X
B
(mp ° C.)

9-1
Me
Me
H
H
Ph

9-2
Me
Me
H
H
Ph(2-F)

9-3
Me
Me
H
H
Ph(2-Cl)

9-4
Me
Me
H
H
Ph(2-OMe)

9-5
Me
Me
H
H
Ph(2,6-F2)
223-226

9-6
Me
Me
H
H
Ph(2,6-Cl2)

9-7
Me
Me
H
H
Ph(2,6-OMe2)

9-8
Me
Me
H
6-Cl
Ph

9-9
Me
Me
H
6-Cl
Ph(2-F)

9-10
Me
Me
H
6-Cl
Ph(2-Cl)

9-11
Me
Me
H
6-Cl
Ph(2,.6-F2)

9-12
Me
Me
H
6-Cl
Ph(2,6-Cl2)

9-13
Me
Me
H
6-Br
Ph

9-14
Me
Me
H
6-Br
Ph(2-F)

9-15
Me
Me
H
6-Br
Ph(2-Cl)

9-16
Me
Me
H
6-Br
Ph(2,6-F2)

9-17
Me
Me
H
6-Br
Ph(2,6-Cl2)

9-18
Me
Me
H
6-CF3
Ph(2,6-F2)

9-19
Me
Me
H
6-CN
Ph(2,6-F2)

9-20
Me
CN
H
H
Ph(2,6-F2)

9-21
Me
CO2Et
H
H
Ph(2,6-F2)

9-22
Me
CN
H
6-Cl
Ph(2,6-F2)

9-23
Me
CO2Et
H
6-Cl
Ph(2,6-F2)

9-24
Me
Et
H
H
Ph(2,6-F2)

9-25
Me
Me
COMe
H
Ph(2,6-F2)

9-26
Me
Me
CH2OMe
H
Ph(2,6-F2)

9-27
Me
Me
H
H
1-naphthyl

9-28
Me
Me
H
H
2-naphthyl

9-29
Me
Me
H
H
2-thienyl

9-30
Me
Me
H
H
3-thienyl

9-31
Me
Me
H
H
2-pyrazinyl

9-32
Me
Me
H
H
2-pyridyl

9-33
Me
Me
H
H
3-pyridyl

9-34
Me
Me
H
H
4-

trifluoromethyl-

3-pyridyl

9-35
Me
Me
H
H
4-pyridyl

9-36
Me
Me
H
H
2-furyl

9-37
Me
Me
H
H
3-furyl

9-38
Me
Me
H
6-OSO2CF3
Ph(2-F)

9-39
Me
Me
H
6-OSO2CF3
Ph(2,6-F2)

9-40
Me
Me
H
6-OCH2CF3
Ph(2-F)

9-41
Me
Me
H
6-OCH2CF3
Ph(2,6-F2)

9-42
Me
Me
H
2-Cl
Ph(2-F)

9-43
Me
Me
H
2-Cl
Ph(2,6-F2)

9-44
Me
Me
H
2-Cl
Ph(2-Cl)

9-45
Me
Me
H
2-Cl
Ph(2-Me)

9-46
Me
Me
H
2-Cl
Ph(2-CF3)

9-47
Me
Me
H
2-Cl
Ph(2-F-6-Cl)

9-48
Me
Me
H
4-Cl
Ph(2-F)

9-49
Me
Me
H
4-Cl
Ph(2,6-F2)

9-50
Me
Me
H
4-Cl
Ph(2-Cl)

9-51
Me
Me
H
4-Cl
Ph(2-Me)

9-52
Me
Me
H
4-Cl
Ph(2-CF3)

9-53
Me
Me
H
4-Cl
Ph(2-F-6-Cl)

9-54
Me
Me
H
5-Cl
Ph(2-F)

9-55
Me
Me
H
5-Cl
Ph(2,6-F2)

9-56
Me
Me
H
5-Cl
Ph(2-Cl)

9-57
Me
Me
H
5-Cl
Ph(2-Me)

9-58
Me
Me
H
5-Cl
Ph(2-CF3)

9-59
Me
Me
H
5-Cl
Ph(2-F-6-Cl)

9-60
Me
Me
H
5-Br
Ph(2-F)

9-61
Me
Me
H
5-Br
Ph(2,6-F2)

9-62
Me
Me
H
5-Br
Ph(2-Cl)

9-63
Me
Me
H
5-Br
Ph(2-Me)

9-64
Me
Me
H
5-Br
Ph(2-CF3)

9-65
Me
Me
H
5-Br
Ph(2-F-6-Cl)

9-66
Me
Me
H
2-Me
Ph(2-F)

9-67
Me
Me
H
2-Me
Ph(2,6-F2)

9-68
Me
Me
H
2-Me
Ph(2-Cl)

9-69
Me
Me
H
2-Me
Ph(2-Me)

9-70
Me
Me
H
2-Me
Ph(2-CF3)

9-71
Me
Me
H
2-Me
Ph(2-F-6-Cl)

9-72
Me
Me
H
4-Me
Ph(2-F)

9-73
Me
Me
H
4-Me
Ph(2,6-F2)

9-74
Me
Me
H
4-Me
Ph(2-Cl)

9-75
Me
Me
H
4-Me
Ph(2-Me)

9-76
Me
Me
H
4-Me
Ph(2-CF3)

9-77
Me
Me
H
4-Me
Ph(2-F-6-Cl)

9-78
Me
Me
H
5-Me
Ph(2-F)

9-79
Me
Me
H
5-Me
Ph(2,6-F2)

9-80
Me
Me
H
5-Me
Ph(2-Cl)

9-81
Me
Me
H
5-Me
Ph(2-Me)

9-82
Me
Me
H
5-Me
Ph(2-CF3)

9-83
Me
Me
H
5-Me
Ph(2-F-6-Cl)

9-84
Me
Me
H
6-Me
Ph(2-F)

9-85
Me
Me
H
6-Me
Ph(2,6-F2)

9-86
Me
Me
H
6-Me
Ph(2-Cl)

9-87
Me
Me
H
6-Me
Ph(2-Me)

9-88
Me
Me
H
6-Me
Ph(2-CF3)

9-89
Me
Me
H
6-Me
Ph(2-F-6-Cl)

9-90
Me
Me
H
5-CN
Ph(2-F)

9-91
Me
Me
H
5-CN
Ph(2,6-F2)

9-92
Me
Me
H
5-CN
Ph(2-Cl)

9-93
Me
Me
H
5-CN
Ph(2-Me)

9-94
Me
Me
H
5-CN
Ph(2-CF3)

9-95
Me
Me
H
5-CN
Ph(2-F-6-Cl)

9-96
Me
Me
H
5-CF3
Ph(2-F)

9-97
Me
Me
H
5-CF3
Ph(2,6-F2)

9-98
Me
Me
H
5-CF3
Ph(2-Cl)

9-99
Me
Me
H
5-CF3
Ph(2-Me)

9-100
Me
Me
H
5-CF3
Ph(2-CF3)

9-101
Me
Me
H
5-CF3
Ph(2-F-6-Cl)

9-102
Me
Me
H
5-OCF3
Ph(2-F)

9-103
Me
Me
H
5-OCF3
Ph(2,6-F2)

9-104
Me
Me
H
5-OCF3
Ph(2-Cl)

9-105
Me
Me
H
5-OCF3
Ph(2-Me)

9-106
Me
Me
H
5-OCF3
Ph(2-CF3)

9-107
Me
Me
H
5-OCF3
Ph(2-F-6-Cl)

9-108
Me
Me
H
6-OCF3
Ph(2-F)

9-109
Me
Me
H
6-OCF3
Ph(2,6-F2)

9-110
Me
Me
H
6-OCF3
Ph(2-Cl)

9-111
Me
Me
H
6-OCF3
Ph(2-Me)

9-112
Me
Me
H
6-OCF3
Ph(2-CF3)

9-113
Me
Me
H
6-OCF3
Ph(2-F-6-Cl)

9-114
Me
Me
H
5-OCHF2
Ph(2-F)

9-115
Me
Me
H
5-OCHF2
Ph(2,6-F2)

9-116
Me
Me
H
5-OCHF2
Ph(2-Cl)

9-117
Me
Me
H
5-OCHF2
Ph(2-Me)

9-118
Me
Me
H
5-OCHF2
Ph(2-CF3)

9-119
Me
Me
H
5-OCHF2
Ph(2-F-6-Cl)

9-120
Me
Me
H
6-OCHF2
Ph(2-F)

9-121
Me
Me
H
6-OCHF2
Ph(2,6-F2)

9-122
Me
Me
H
6-OCHF2
Ph(2-Cl)

9-123
Me
Me
H
6-OCHF2
Ph(2-Me)

9-124
Me
Me
H
6-OCHF2
Ph(2-CF3)

9-125
Me
Me
H
6-OCHF2
Ph(2-F-6-Cl)

9-126
Me
Me
H
2,6-Cl2
Ph(2-F)

9-127
Me
Me
H
2,6-Cl2
Ph(2,6-F2)

9-128
Me
Me
H
2,6-Cl2
Ph(2-Cl)

9-129
Me
Me
H
2,6-Cl2
Ph(2-Me)

9-130
Me
Me
H
2,6-Cl2
Ph(2-CF3)

9-131
Me
Me
H
2,6-Cl2
Ph(2-F-6-Cl)

9-132
Me
Me
H
4,6-Cl2
Ph(2-F)

9-133
Me
Me
H
4,6-Cl2
Ph(2,6-F2)

9-134
Me
Me
H
4,6-Cl2
Ph(2-Cl)

9-135
Me
Me
H
4,6-Cl2
Ph(2-Me)

9-136
Me
Me
H
4,6-Cl2
Ph(2-CF3)

9-137
Me
Me
H
4,6-Cl2
Ph(2-F-6-Cl)

9-138
Me
Me
H
5,6-Cl2
Ph(2-F)

9-139
Me
Me
H
5,6-Cl2
Ph(2,6-F2)

9-140
Me
Me
H
5,6-Cl2
Ph(2-Cl)

9-141
Me
Me
H
5,6-Cl2
Ph(2-Me)

9-142
Me
Me
H
5,6-Cl2
Ph(2-CF2)

9-143
Me
Me
H
5,6-Cl2
Ph(2-F-6-Cl)

9-144
Me
Me
H
2-Cl-6-Br
Ph(2-F)

9-145
Me
Me
H
2-C1-6-Br
Ph(2,6-F2)

9-146
Me
Me
H
2-Cl-6-Br
Ph(2-Cl)

9-147
Me
Me
H
2-Cl-6-Br
Ph(2-Me)

9-148
Me
Me
H
2-Cl-6-Br
Ph(2-CF3)

9-149
Me
Me
H
2-Cl-6-Br
Ph(2-F-6-Cl)

9-150
Me
Me
H
4-C1-6-Br
Ph(2-F)

9-151
Me
Me
H
4-Cl-6-Br
ph(2,6-F2)

9-152
Me
Me
H
4-Cl-6-Br
Ph(2-Cl)

9-153
Me
Me
H
4-Cl-6-Br
Ph(2-Me)

9-154
Me
Me
H
4-Cl-6-Br
Ph(2-CF3)

9-155
Me
Me
H
4-Cl-6-Br
Ph(2-F-6-Cl)

9-156
Me
Me
H
5-Cl-6-Br
Ph(2-F)

9-157
Me
Me
H
5-Cl-6-Br
Ph(2,6-F2)

9-158
Me
Me
H
5-Cl-6-Br
Ph(2-Cl)

9-159
Me
Me
H
5-Cl-6-Br
Ph(2-Me)

9-160
Me
Me
H
5-Cl-6-Br
Ph(2-CF3)

9-161
Me
Me
H
5-Cl-6-Br
Ph(2-F-6-Cl)

9-162
Me
Me
H
2-Cl-6-CF3
Ph(2-F)

9-163
Me
Me
H
2-Cl-6-CF3
Ph(2,6-F2)

9-164
Me
Me
H
2-Cl-6-CF3
Ph(2-Cl)

9-165
Me
Me
H
2-Cl-6-CF3
Ph(2-Me)

9-166
Me
Me
H
2-Cl-6-CF3
Ph(2-CF3)

9-167
Me
Me
H
2-Cl-6-CF3
Ph(2-F-6-Cl)

9-168
Me
Me
H
4-Cl-6-CF3
Ph(2-F)

9-169
Me
Me
H
4-Cl-6-CF3
Ph(2,6-F2)

9-170
Me
Me
H
4-Cl-6-CF3
Ph(2-Cl)

9-171
Me
Me
H
4-Cl-6-CF3
Ph(2-Me)

9-172
Me
Me
H
4-Cl-6-CF3
Ph(2-CF3)

9-173
Me
Me
H
4-Cl-6-CF3
Ph(2-F-6-Cl)

9-174
Me
Me
H
5-Cl-6-CF3
Ph(2-F)

9-175
Me
Me
H
5-Cl-6-CF3
Ph(2,6-F2)

9-176
Me
Me
H
5-Cl-6-CF3
Ph(2-Cl)

9-177
Me
Me
H
5-Cl-6-CF3
Ph(2-Me)

9-178
Me
Me
H
5-Cl-6-CF3
Ph(2-CF3)

9-179
Me
Me
H
5-Cl-6-CF3
Ph(2-F-6-Cl)

9-180
Me
Me
H
2-Cl-6-OCF3
Ph(2-F)

9-181
Me
Me
H
2-Cl-6-OCF3
Ph(2,6-F2)

9-182
Me
Me
H
2-Cl-6-OCF3
Ph(2-Cl)

9-183
Me
Me
H
2-Cl-6-OCF3
Ph(2-Me)

9-184
Me
Me
H
2-Cl-6-OCF3
Ph(2-CF3)

9-185
Me
Me
H
2-Cl-6-OCF3
Ph(2-F-6-Cl)

9-186
Me
Me
H
4-Cl-6-OCF3
Ph(2-F)

9-187
Me
Me
H
4-Cl-6-OCF3
Ph(2,6-F2)

9-188
Me
Me
H
4-Cl-6-OCF3
Ph(2-Cl)

9-189
Me
Me
H
4-Cl-6-OCF3
Ph(2-Me)

9-190
Me
Me
H
4-Cl-6-OCF3
Ph(2-CF3)

9-191
Me
Me
H
4-Cl-6-OCF3
Ph(2-F-6-Cl)

9-192
Me
Me
H
5-Cl-6-OCF3
Ph(2-F)

9-193
Me
Me
H
5-Cl-6-OCF3
Ph(2,6-F2)

9-194
Me
Me
H
5-Cl-6-OCF3
Ph(2-Cl)

9-195
Me
Me
H
5-Cl-6-OCF3
Ph(2-Me)

9-196
Me
Me
H
5-Cl-6-OCF3
Ph(2-CF3)

9-197
Me
Me
H
5-Cl-6-OCF3
Ph(2-F-6-Cl)

9-198
Me
Me
H
2-Cl-6-OCHF2
Ph(2-F)

9-199
Me
Me
H
2-Cl-6-OCHF2
Ph(2,6-F2)

9-200
Me
Me
H
2-Cl-6-OCHF2
Ph(2-Cl)

9-201
Me
Me
H
2-Cl-6-OCHF2
Ph(2-Me)

9-202
Me
Me
H
2-Cl-6-OCHF2
Ph(2-CF3)

9-203
Me
Me
H
2-Cl-6-OCHF2
Ph(2-F-6-Cl)

9-204
Me
Me
H
4-Cl-6-OCHF2
Ph(2-F)

9-205
Me
Me
H
4-Cl-6-OCHF2
Ph(2,6-F2)

9-206
Me
Me
H
4-Cl-6-OCHF2
Ph(2-Cl)

9-207
Me
Me
H
4-Cl-6-OCHF2
Ph(2-Me)

9-208
Me
Me
H
4-Cl-6-OCHF2
Ph(2-CF3)

9-209
Me
Me
H
4-Cl-6-OCHF2
Ph(2-F-6-Cl)

9-210
Me
Me
H
5-Cl-6-OCHF2
Ph(2-F)

9-211
Me
Me
H
5-Cl-6-OCHF2
Ph(2,6-F2)

9-212
Me
Me
H
5-Cl-6-OCHF2
Ph(2-Cl)

9-213
Me
Me
H
5-Cl-6-OCHF2
Ph(2-Me)

9-214
Me
Me
H
5-Cl-6-OCHF2
Ph(2-CF3)

9-215
Me
Me
H
5-Cl-6-OCHF2
Ph(2-F-6-Cl)

9-216
Me
Me
H
2-Cl-6-OCH2CF3
Ph(2-F)

9-217
Me
Me
H
2-Cl-6-OCH2CF3
Ph(2,6-F2)

9-218
Me
Me
H
2-Cl-6-OCH2CF3
Ph(2-Cl)

9-219
Me
Me
H
2-Cl-6-OCH2CF3
Ph(2-Me)

9-220
Me
Me
H
2-Cl-6-OCH2CF3
Ph(2-CF3)

9-221
Me
Me
H
2-Cl-6-OCH2CF3
Ph(2-F-6-Cl)

9-222
Me
Me
H
4-Cl-6-OCH2CF3
Ph(2-F)

9-223
Me
Me
H
4-Cl-6-OCH2CF3
Ph(2,6-F2)

9-224
Me
Me
H
4-Cl-6-OCH2CF3
Ph(2-Cl)

9-225
Me
Me
H
4-Cl-6-OCH2CF3
Ph(2-Me)

9-226
Me
Me
H
4-Cl-6-OCH2CF3
Ph(2-CF3)

9-227
Me
Me
H
4-Cl-6-OCH2CF3
Ph(2-F-6-Cl)

9-228
Me
Me
H
5-Cl-6-OCH2CF3
Ph(2-F)

9-229
Me
Me
H
5-Cl-6-OCH2CF3
Ph(2,6-F2)

9-230
Me
Me
H
5-Cl-6-OCH2CF3
Ph(2-Cl)

9-231
Me
Me
H
5-Cl-6-OCH2CF3
Ph(2-Me)

9-232
Me
Me
H
5-Cl-6-OCH2CF3
Ph(2-CF3)

9-233
Me
Me
H
5-Cl-6-OCH2CF3
Ph(2-F-6-Cl)

9-234
Me
Me
H
2-Me-6-Cl
Ph(2-F)

9-235
Me
Me
H
2-Me-6-Cl
Ph(2,6-F2)

9-236
Me
Me
H
2-Me-6-Cl
Ph(2-Cl)

9-237
Me
Me
H
2-Me-6-Cl
Ph(2-Me)

9-238
Me
Me
H
2-Me-6-Cl
Ph(2-CF3)

9-239
Me
Me
H
2-Me-6-Cl
Ph(2-F-6-Cl)

9-240
Me
Me
H
4-Me-6-Cl
Ph(2-F)

9-241
Me
Me
H
4-Me-6-Cl
Ph(2,6-F2)

9-242
Me
Me
H
4-Me-6-Cl
Ph(2-Cl)

9-243
Me
Me
H
4-Me-6-Cl
Ph(2-Me)

9-244
Me
Me
H
4-Me-6-Cl
Ph(2-CF3)

9-245
Me
Me
H
4-Me-6-Cl
Ph(2-F-6-Cl)

9-246
Me
Me
H
5-Me-6-Cl
Ph(2-F)

9-247
Me
Me
H
5-Me-6-Cl
Ph(2,6-F2)

9-248
Me
Me
H
5-Me-6-Cl
Ph(2-Cl)

9-249
Me
Me
H
5-Me-6-Cl
Ph(2-Me)

9-250
Me
Me
H
5-Me-6-Cl
Ph(2-CF3)

9-251
Me
Me
H
5-Me-6-Cl
Ph(2-F-6-Cl)

9-252
Me
Me
H
2-Me-6-Br
Ph(2-F)

9-253
Me
Me
H
2-Me-6-Br
Ph(2,6-F2)

9-254
Me
Me
H
2-Me-6-Br
Ph(2-Cl)

9-255
Me
Me
H
2-Me-6-Br
Ph(2-Me)

9-256
Me
Me
H
2-Me-6-Br
Ph(2-CF3)

9-257
Me
Me
H
2-Me-6-Br
Ph(2-F-6-Cl)

9-258
Me
Me
H
4-Me-6-Br
Ph(2-F)

9-259
Me
Me
H
4-Me-6-Br
Ph(2,6-F2)

9-260
Me
Me
H
4-Me-6-Br
Ph(2-Cl)

9-261
Me
Me
H
4-Me-6-Br
Ph(2-Me)

9-262
Me
Me
H
4-Me-6-Br
Ph(2-CF3)

9-263
Me
Me
H
4-Me-6-Br
Ph(2-F-6-Cl)

9-264
Me
Me
H
5-Me-6-Br
Ph(2-F)

9-265
Me
Me
H
5-Me-6-Br
Ph(2,6-F2)

9-266
Me
Me
H
5-Me-6-Br
Ph(2-Cl)

9-267
Me
Me
H
5-Me-6-Br
Ph(2-Me)

9-268
Me
Me
H
5-Me-6-Br
Ph(2-CF3)

9-269
Me
Me
H
5-Me-6-Br
Ph(2-F-6-Cl)

9-270
Me
Me
H
2-Me-6-CF3
Ph(2-F)

9-271
Me
Me
H
2-Me-6-CF3
Ph(2,6-F2)

9-272
Me
Me
H
2-Me-6-CF3
Ph(2-Cl)

9-273
Me
Me
H
2-Me-6-CF3
Ph(2-Me)

9-274
Me
Me
H
2-Me-6-CF3
Ph(2-CF3)

9-275
Me
Me
H
2-Me-6-CF3
Ph(2-F-6-Cl)

9-276
Me
Me
H
4-Me-6-CF3
Ph(2-F)

9-277
Me
Me
H
4-Me-6-CF3
Ph(2,6-F2)

9-278
Me
Me
H
4-Me-6-CF3
Ph(2-Cl)

9-279
Me
Me
H
4-Me-6-CF3
Ph(2-Me)

9-280
Me
Me
H
4-Me-6-CF3
Ph(2-CF3)

9-281
Me
Me
H
4-Me-6-CF3
Ph(2-F-6-Cl)

9-282
Me
Me
H
5-Me-6-CF3
Ph(2-F)

9-283
Me
Me
H
5-Me-6-CF3
Ph(2,6-F2)

9-284
Me
Me
H
5-Me-6-CF3
Ph(2-Cl)

9-285
Me
Me
H
5-Me-6-CF3
Ph(2-Me)

9-286
Me
Me
H
5-Me-6-CF3
Ph(2-CF3)

9-287
Me
Me
H
5-Me-6-CF3
Ph(2-F-6-Cl)

9-288
Me
Me
H
2-Me-6-OCF3
Ph(2-F)

9-289
Me
Me
H
2-Me-6-OCF3
Ph(2,6-F2)

9-290
Me
Me
H
2-Me-6-OCF3
Ph(2-Cl)

9-291
Me
Me
H
2-Me-6-OCF3
Ph(2-Me)

9-292
Me
Me
H
2-Me-6-OCF3
Ph(2-CF3)

9-293
Me
Me
H
2-Me-6-OCF3
Ph(2-F-6-Cl)

9-294
Me
Me
H
4-Me-6-OCF3
Ph(2-F)

9-295
Me
Me
H
4-Me-6-OCF3
Ph(2,6-F2)

9-296
Me
Me
H
4-Me-6-OCF3
Ph(2-Cl)

9-297
Me
Me
H
4-Me-6-OCF3
Ph(2-Me)

9-298
Me
Me
H
4-Me-6-OCF3
Ph(2-CF3)

9-299
Me
Me
H
4-Me-6-OCF3
Ph(2-F-6-Cl)

9-300
Me
Me
H
5-Me-6-OCF3
Ph(2-F)

9-301
Me
Me
H
5-Me-6-OCF3
Ph(2,6-F2)

9-302
Me
Me
H
5-Me-6-OCF3
Ph(2-Cl)

9-303
Me
Me
H
5-Me-6-OCF3
Ph(2-Me)

9-304
Me
Me
H
5-Me-6-OCF3
Ph(2-CF3)

9-305
Me
Me
H
5-Me-6-OCF3
Ph(2-F-6-Cl)

9-306
Me
Me
H
2-Me-6-OCHF2
Ph(2-F)

9-307
Me
Me
H
2-Me-6-OCHF2
Ph(2,6-F2)

9-308
Me
Me
H
2-Me-6-OCHF2
Ph(2-Cl)

9-309
Me
Me
H
2-Me-6-OCHF2
Ph(2-Me)

9-310
Me
Me
H
2-Me-6-OCHF2
Ph(2-CF3)

9-311
Me
Me
H
2-Me-6-OCHF2
Ph(2-F-6-Cl)

9-312
Me
Me
H
4-Me-6-OCHF2
Ph(2-F)

9-313
Me
Me
H
4-Me-6-OCHF2
Ph(2,6-F2)

9-314
Me
Me
H
4-Me-6-OCHF2
Ph(2-Cl)

9-315
Me
Me
H
4-Me-6-OCHF2
Ph(2-Me)

9-316
Me
Me
H
4-Me-6-OCHF2
Ph(2-CF3)

9-317
Me
Me
H
4-Me-6-OCHF2
Ph(2-F-6-Cl)

9-318
Me
Me
H
5-Me-6-OCHF2
Ph(2-F)

9-319
Me
Me
H
5-Me-6-OCHF2
Ph(2,6-F2)

9-320
Me
Me
H
5-Me-6-OCHF2
Ph(2-Cl)

9-321
Me
Me
H
5-Me-6-OCHF2
Ph(2-Me)

9-322
Me
Me
H
5-Me-6-OCHF2
Ph(2-CF3)

9-323
Me
Me
H
5-Me-6-OCHF2
Ph(2-F-6-Cl)

9-324
Me
Me
H
2-Me-6-OCH2CF3
Ph(2-F)

9-325
Me
Me
H
2-Me-6-OCH2CF3
Ph(2,6-F2)

9-326
Me
Me
H
2-Me-6-OCH2CF3
Ph(2-Cl)

9-327
Me
Me
H
2-Me-6-OCH2CF3
Ph(2-Me)

9-328
Me
Me
H
2-Me-6-OCH2CF3
Ph(2-CF3)

9-329
Me
Me
H
2-Me-6-OCH2CF3
Ph(2-F-6-Cl)

9-330
Me
Me
H
4-Me-6-OCH2CF3
Ph(2-F)

9-331
Me
Me
H
4-Me-6-OCH2CF3
Ph(2,6-F2)

9-332
Me
Me
H
4-Me-6-OCH2CF3
Ph(2-Cl)

9-333
Me
Me
H
4-Me-6-OCH2CF3
Ph(2-Me)

9-334
Me
Me
H
4-Me-6-OCH2CF3
Ph(2-CF3)

9-335
Me
Me
H
4-Me-6-OCH2CF2
Ph(2-F-6-Cl)

9-336
Me
Me
H
5-Me-6-OCH2CF3
Ph(2-F)

9-337
Me
Me
H
5-Me-6-OCH2CF3
Ph(2,6-F2)

9-338
Me
Me
H
5-Me-6-OCH2CF3
Ph(2-Cl)

9-339
Me
Me
H
5-Me-6-OCH2CF3
Ph(2-Me)

9-340
Me
Me
H
5-Me-6-OCH2CF3
Ph(2-CF3)

9-341
Me
Me
H
5-Me-6-OCH2CF3
Ph(2-F-6-Cl)

[0249]

10

TABLE 10

Physical

Compound

properties

No.
R1
R2
R3
X
B
(mp ° C.)

10-1
Me
Me
H
H
Ph

10-2
Me
Me
H
H
Ph(2-F)

10-3
Me
Me
H
H
Ph(2-Cl)

10-4
Me
Me
H
H
Ph(2-OMe)

10-5
Me
Me
H
H
Ph(2,6-F2)
155-157

10-6
Me
Me
H
H
Ph(2,6-Cl2)

10-7
Me
Me
H
H
Ph(2,6-OMe2)

10-8
Me
Me
H
2-Cl
Ph

10-9
Me
Me
H
2-Cl
Ph(2-F)

10-10
Me
Me
H
2-Cl
Ph(2-Cl)

10-11
Me
Me
H
2-Cl
Ph(2,6-F2)

10-12
Me
Me
H
2-Cl
Ph(2,6-Cl2)

10-13
Me
Me
H
2-Br
Ph

19-14
Me
Me
H
2-Br
Ph(2-F)

10-15
Me
Me
H
2-Br
Ph(2-Cl)

10-16
Me
Me
H
2-Br
Ph(2,6-F2)

10-17
Me
Me
H
2-Br
Ph(2,6-Cl2)

10-18
Me
Me
H
2-CF3
Ph(2,6-F2)

10-19
Me
Me
H
2-CN
Ph(2,6-F2)

10-20
Me
CN
H
H
Ph(2,6-F2)

10-21
Me
CO2Et
H
H
Ph(2,6-F2)

10-22
Me
CN
H
2-Cl
Ph(2,6-F2)

10-23
Me
CO2Et
H
2-Cl
Ph(2,6-F2)

10-24
Me
Et
H
H
Ph(2,6-F2)

10-25
Me
Me
COMe
H
Ph(2,6-F2)

10-26
Me
Me
CH2OMe
H
Ph(2,6-F2)

10-27
Me
Me
H
H
1-naphthyl

10-28
Me
Me
H
H
2-naphthyl

10-29
Me
Me
H
H
2-thienyl

10-30
Me
Me
H
H
3-thienyl

10-31
Me
Me
H
H
2-pyrazinyl

10-32
Me
Me
H
H
2-pyridyl

10-33
Me
Me
H
H
3-pyridyl

10-34
Me
Me
H
H
4-

trifluoromethyl-

3-pyridyl

10-35
Me
Me
H
H
4-pyridyl

10-36
Me
Me
H
H
2-furyl

10-37
Me
Me
H
H
3-furyl

10-38
Me
Me
H
3-Cl
Ph(2-F)

10-39
Me
Me
H
3-Cl
Ph(2,6-F2)

10-40
Me
Me
H
3-Cl
Ph(2-Cl)

10-41
Me
Me
H
3-Cl
Ph(2-Me)

10-42
Me
Me
H
3-Cl
Ph(2-CF3)

10-43
Me
Me
H
3-Cl
Ph(2-F-6-Cl)

10-44
Me
Me
H
3-Br
Ph(2-F)

10-45
Me
Me
H
3-Br
Ph(2,6-F2)

10-46
Me
Me
H
3-Br
Ph(2-Cl)

10-47
Me
Me
H
3-Br
Ph(2-Me)

10-48
Me
Me
H
3-Br
Ph(2-CF3)

10-49
Me
Me
H
3-Br
Ph(2-F-6-Cl)

10-50
Me
Me
H
2-Me
Ph(2-F)

10-51
Me
Me
H
2-Me
Ph(2,6-F2)

10-52
Me
Me
H
2-Me
Ph(2-Cl)

10-53
Me
Me
H
2-Me
Ph(2-Me)

10-54
Me
Me
H
2-Me
Ph(2-CF3)

10-55
Me
Me
H
2-Me
Ph(2-F-6-Cl)

10-56
Me
Me
H
3-Me
Ph(2-F)

10-57
Me
Me
H
3-Me
Ph(2,6-F2)

10-58
Me
Me
H
3-Me
Ph(2-Cl)

10-59
Me
Me
H
3-Me
Ph(2-Me)

10-60
Me
Me
H
3-Me
Ph(2-CF3)

10-61
Me
Me
H
3-Me
Ph(2-F-6-Cl)

10-62
Me
Me
H
3-CN
Ph(2-F)

10-63
Me
Me
H
3-CN
Ph(2,6-F2)

10-64
Me
Me
H
3-CN
Ph(2-Cl)

10-65
Me
Me
H
3-CN
Ph(2-Me)

10-66
Me
Me
H
3-CN
Ph(2-CF3)

10-67
Me
Me
H
3-CN
Ph(2-F-6-Cl)

10-68
Me
Me
H
3-CF3
Ph(2-F)

10-69
Me
Me
H
3-CF3
Ph(2,6-F2)

10-70
Me
Me
H
3-CF3
Ph(2-Cl)

10-71
Me
Me
H
3-CF3
Ph(2-Me)

10-72
Me
Me
H
3-CF3
Ph(2-CF3)

10-73
Me
Me
H
3-CF3
Ph(2-F-6-Cl)

10-74
Me
Me
H
2-OCF3
Ph(2-F)

10-75
Me
Me
H
2-OCF3
Ph(2,6-F2)

10-76
Me
Me
H
2-OCF3
Ph(2-Cl)

10-77
Me
Me
H
2-OCF3
Ph(2-Me)

10-78
Me
Me
H
2-OCF3
Ph(2-CF3)

10-79
Me
Me
H
2-OCF3
Ph(2-F-6-Cl)

10-80
Me
Me
H
3-OCF3
Ph(2-F)

10-81
Me
Me
H
3-OCF3
Ph(2,6-F2)

10-82
Me
Me
H
3-OCF3
Ph(2-Cl)

10-83
Me
Me
H
3-OCF3
Ph(2-Me)

10-84
Me
Me
H
3-OCF3
Ph(2-CF3)

10-85
Me
Me
H
3-OCF3
Ph(2-F-6-Cl)

10-86
Me
Me
H
2-OCHF2
Ph(2-F)

10-87
Me
Me
H
2-OCHF2
Ph(2,6-F2)

10-88
Me
Me
H
2-OCHF2
Ph(2-Cl)

10-89
Me
Me
H
2-OCHF2
Ph(2-Me)

10-90
Me
Me
H
2-OCHF2
Ph(2-CF3)

10-91
Me
Me
H
2-OCHF2
Ph(2-F-6-Cl)

10-92
Me
Me
H
3-OCHF2
Ph(2-F)

10-93
Me
Me
H
3-OCHF2
Ph(2,6-F2)

10-94
Me
Me
H
3-OCHF2
Ph(2-Cl)

10-95
Me
Me
H
3-OCHF2
Ph(2-Me)

10-96
Me
Me
H
3-OCHF2
Ph(2-CF3)

10-97
Me
Me
H
3-OCHF2
Ph(2-F-6-Cl)

10-98
Me
Me
H
2-CF3-3-Cl
Ph(2-F)

10-99
Me
Me
H
2-CF3-3-Cl
Ph(2,6-F2)

10-100
Me
Me
H
2-CF3-3-Cl
Ph(2-Cl)

10-101
Me
Me
H
2-CF3-3-Cl
Ph(2-Me)

10-102
Me
Me
H
2-CF3-3-Cl
Ph(2-CF3)

10-103
Me
Me
H
2-CF3-3-Cl
Ph(2-F-6-Cl)

10-104
Me
Me
H
2-CF3-3-Me
Ph(2-F)

10-105
Me
Me
H
2-CF3-3-Me
Ph(2,6-F2)

10-106
Me
Me
H
2-CF3-3-Me
Ph(2-Cl)

10-107
Me
Me
H
2-CF3-3-Me
Ph(2-Me)

10-108
Me
Me
H
2-CF3-3-Me
Ph(2-CF3)

10-109
Me
Me
H
2-CF3-3-Me
Ph(2-F-6-Cl)

10-110
Me
Me
H
2-OMe-3-Cl
Ph(2-F)

10-111
Me
Me
H
2-OMe-3-Cl
Ph(2,6-F2)

10-112
Me
Me
H
2-OMe-3-Cl
Ph(2-Cl)

10-113
Me
Me
H
2-OMe-3-Cl
Ph(2-Me)

10-114
Me
Me
H
2-OMe-3-Cl
Ph(2-CF3)

10-115
Me
Me
H
2-OMe-3-Cl
Ph(2-F-6-Cl)

10-116
Me
Me
H
2-OMe-3-Me
Ph(2-F)

10-117
Me
Me
H
2-OMe-3-Me
Ph(2,6-F2)

10-118
Me
Me
H
2-OMe-3-Me
Ph(2-Cl)

10-119
Me
Me
H
2-OMe-3-Me
Ph(2-Me)

10-120
Me
Me
H
2-OMe-3-Me
Ph(2-CF3)

10-121
Me
Me
H
2-OMe-3-Me
Ph(2-F-6-Cl)

10-122
Me
Me
H
2-OCF3-3-Cl
Ph(2-F)

10-123
Me
Me
H
2-OCF3-3-Cl
Ph(2,6-F2)

10-124
Me
Me
H
2-OCF3-3-Cl
Ph(2-Cl)

10-125
Me
Me
H
2-OCF3-3-Cl
Ph(2-Me)

10-126
Me
Me
H
2-OCF3-3-Cl
Ph(2-CF3)

10-127
Me
Me
H
2-OCF3-3-Cl
Ph(2-F-6-Cl)

10-128
Me
Me
H
2-OCF3-3-Me
Ph(2-F)

10-129
Me
Me
H
2-OCF3-3-Me
Ph(2,6-F2)

10-130
Me
Me
H
2-OCF3-3-Me
Ph(2-Cl)

10-131
Me
Me
H
2-OCF3-3-Me
Ph(2-Me)

10-132
Me
Me
H
2-OCF3-3-Me
Ph(2-CF3)

10-133
Me
Me
H
2-OCF3-3-Me
Ph(2-F-6-Cl)

10-134
Me
Me
H
2-OCHF2-3-Cl
Ph(2-F)

10-135
Me
Me
H
2-OCHF2-3-Cl
Ph(2,6-F2)

10-136
Me
Me
H
2-OCHF2-3-Cl
Ph(2-Cl)

10-137
Me
Me
H
2-OCHF2-3-Cl
Ph(2-Me)

10-138
Me
Me
H
2-OCHF2-3-Cl
Ph(2-CF3)

10-139
Me
Me
H
2-OCHF2-3-Cl
Ph(2-F-6-Cl)

10-140
Me
Me
H
2-OCHF2-3-Me
Ph(2-F)

10-141
Me
Me
H
2-OCHF2-3-Me
Ph(2,6-F2)

10-142
Me
Me
H
2-OCHF2-3-Me
Ph(2-Cl)

10-143
Me
Me
H
2-OCHF2-3-Me
Ph(2-Me)

10-144
Me
Me
H
2-OCHF2-3-Me
Ph(2-CF3)

10-145
Me
Me
H
2-OCHF2-3-Me
Ph(2-F-6-Cl)

[0250]

11

TABLE 11

Physical

Compound

properties

No.
R1
R2
R3
X
B
(mp ° C.)

11-1
Me
Me
H
H
Ph

11-2
Me
Me
H
H
Ph(2-F)
94-96

11-3
Me
Me
H
H
Ph(2-Cl)

11-4
Me
Me
H
H
Ph(2-OMe)

11-5
Me
Me
H
H
Ph(2,6-F2)
119-121

11-6
Me
Me
H
H
Ph(2,6-Cl2)

11-7
Me
Me
H
H
Ph(2,6-OMe2)

11-8
Me
Me
H
6-Cl
Ph

11-9
Me
Me
H
6-Cl
Ph(2-F)

11-10
Me
Me
H
6-Cl
ph(2-Cl)

11-11
Me
Me
H
6-Cl
Ph(2,6-F2)

11-12
Me
Me
H
6-Cl
ph(2,6-Cl2)

11-13
Me
Me
H
6-Br
Ph

11-14
Me
Me
H
6-Br
Ph(2-F)

11-15
Me
Me
H
6-Br
Ph(2-Cl)

11-16
Me
Me
H
6-Br
Ph(2,6-F2)

11-17
Me
Me
H
6-Br
Ph(2,6-Cl2)

11-18
Me
Me
H
6-CF3
Ph(2,6-F2)

11-19
Me
Me
H
6-CN
Ph(2,6-F2)

11-20
Me
CN
H
H
Ph(2,6-F2)

11-21
Me
CO2Et
H
H
Ph(2,6-F2)

11-22
Me
CN
H
6-Cl
Ph(2,6-F2)

11-23
Me
CO2Et
H
6-Cl
Ph(2,6-F2)

11-24
Me
Et
H
H
Ph(2,6-F2)

11-25
Me
Me
COMe
H
Ph(2,6-F2)

11-26
Me
Me
CH2OMe
H
Ph(2,6-F2)

11-27
Me
Me
H
H
1-naphthyl

11-28
Me
Me
H
H
2-naphthyl

11-29
Me
Me
H
H
2-thienyl

11-30
Me
Me
H
H
3-thienyl

11-31
Me
Me
H
H
2-pyrazinyl

11-32
Me
Me
H
H
2-pyridyl

11-33
Me
Me
H
H
3-pyridyl

11-34
Me
Me
H
H
4-

trifluoromethyl-

3-pyridyl

11-35
Me
Me
H
H
4-pyridyl

11-36
Me
Me
H
H
2-furyl

11-37
Me
Me
H
H
3-furyl

11-38
Me
Me
H
2-Cl
Ph(2-F)

11-39
Me
Me
H
2-Cl
Ph(2,6-F2)

11-40
Me
Me
H
2-Cl
Ph(2-Cl)

11-41
Me
Me
H
2-Cl
Ph(2-Me)

11-42
Me
Me
H
2-Cl
Ph(2-CF3)

11-43
Me
Me
H
2-Cl
Ph(2-F-6-Cl)

11-44
Me
Me
H
2-Me
Ph(2-F)

11-45
Me
Me
H
2-Me
Ph(2,6-F2)

11-46
Me
Me
H
2-Me
Ph(2-Cl)

11-47
Me
Me
H
2-Me
Ph(2-Me)

11-48
Me
Me
H
2-Me
Ph(2-CF3)

11-49
Me
Me
H
2-Me
Ph(2-F-6-Cl)

[0251]

12

TABLE 12

Physical

Compound

properties

No.
R1
R2
R3
X
B
(mp ° C.)

12-1
Me
Me
H
H
Ph

12-2
Me
Me
H
H
Ph(2-F)
180-183

12-3
Me
Me
H
H
Ph(2-Cl)

12-4
Me
Me
H
H
Ph(2-OMe)

12-5
Me
Me
H
H
Ph(2,6-F2)
246-250

12-6
Me
Me
H
H
Ph(2,6-Cl2)

12-7
Me
Me
H
H
Ph(2,6-OMe2)

12-8
Me
Me
H
6-Cl
Ph

12-9
Me
Me
H
6-Cl
Ph(2-F)

12-10
Me
Me
H
6-Cl
Ph(2-Cl)

12-11
Me
Me
H
6-Cl
Ph(2,6-F2)

12-12
Me
Me
H
6-Cl
Ph(2,6-Cl2)

12-13
Me
Me
H
6-Br
Ph

12-14
Me
Me
H
6-Br
Ph(2-F)

12-15
Me
Me
H
6-Br
Ph(2-Cl)

12-16
Me
Me
H
6-Br
Ph(2,6-F2)

12-17
Me
Me
H
6-Br
Ph(2,6-Cl2)

12-18
Me
Me
H
6-CF3
Ph(2,6-F2)

12-19
Me
Me
H
6-CN
Ph(2,6-F2)

12-20
Me
CN
H
H
Ph(2,6-F2)

12-21
Me
CO2Et
H
H
Ph(2,6-F2)

12-22
Me
CN
H
6-Cl
Ph(2,6-F2)

12-23
Me
CO2Et
H
6-Cl
Ph(2,6-F2)

12-24
Me
Et
H
H
Ph(2,6-F2)

12-25
Me
Me
COMe
H
Ph(2,6-F2)

12-26
Me
Me
CH2OMe
H
Ph(2,6-F2)

12-27
Me
Me
H
H
1-naphthyl

12-28
Me
Me
H
H
2-naphthyl

12-29
Me
Me
H
H
2-thienyl

12-30
Me
Me
H
H
3-thienyl

12-31
Me
Me
H
H
2-pyrazinyl

12-32
Me
Me
H
H
2-pyridyl

12-33
Me
Me
H
H
3-pyridyl

12-34
Me
Me
H
H
4-

trifluoromethyl-

3-pyridyl

12-35
Me
Me
H
H
4-pyridyl

12-36
Me
Me
H
H
2-furyl

12-37
Me
Me
H
H
3-furyl

12-38
Me
Me
H
2-Cl
Ph(2-F)

12-39
Me
Me
H
2-Cl
Ph(2,6-F2)

12-40
Me
Me
H
2-Cl
Ph(2-Cl)

12-41
Me
Me
H
2-Cl
Ph(2-Me)

12-42
Me
Me
H
2-Cl
Ph(2-CF3)

12-43
Me
Me
H
2-Cl
Ph(2-F-6-Cl)

12-44
Me
Me
H
2-Me
Ph(2-F)

12-45
Me
Me
H
2-Me
Ph(2,6-F2)

12-46
Me
Me
H
2-Me
Ph(2-Cl)

12-47
Me
Me
H
2-Me
Ph(2-Me)

12-48
Me
Me
H
2-Me
Ph(2-CF3)

12-49
Me
Me
H
2-Me
Ph(2-F-6-Cl)

[0252]

13

TABLE 13

Com-

Physical

pound

properties

No.
R1
R2
R3
X1
X2
X3
X4
B
(mp ° C.)

13-1
Me
Me
H
H
H
H
H
Ph

13-2
Me
Me
H
H
H
H
H
Ph(2-Cl)
Oil

13-3
Me
Me
H
H
H
H
H
Ph(4-Cl)

13-4
Me
Me
H
H
H
H
H
Ph(2-CF3)
164-167

13-5
Me
Me
H
H
H
H
H
Ph(4-CF3)

13-6
Me
Me
H
H
H
H
H
Ph(2-F)
116-121

13-7
Me
Me
H
H
H
H
H
Ph(2,6-F2)
134-139

13-8
Me
Me
H
H
H
H
H
Ph(2-OCF3)

13-9
Me
Me
H
H
H
H
H
Ph(2-OCHF2)

13-10
Me
Me
H
H
H
H
H
Ph(2-OMe)

13-11
Me
Me
H
H
H
H
H
Ph(2,6-(OMe)2)

13-12
Me
Me
H
F
F
H
H
Ph(2-NO2)

13-13
Me
Me
H
F
F
H
H
Ph

13-14
Me
Me
H
F
F
H
H
Ph(2-Cl)

13-15
Me
Me
H
F
F
H
H
Ph(4-Cl)

13-16
Me
Me
H
F
F
H
H
Ph(2-CF3)

13-17
Me
Me
H
F
F
H
H
Ph(4-CF3)

13-18
Me
Me
H
F
F
H
H
Ph(2-F)
114-117

13-19
Me
Me
H
F
F
H
H
Ph(2,6-F2)
123-125

13-20
Me
Me
H
F
F
H
H
Ph(2-OCF3)

13-21
Me
Me
H
F
F
H
H
Ph(2-OCHF2)

13-22
Me
Me
H
F
F
H
H
Ph(2-OMe)

13-23
Me
Me
H
F
F
H
H
Ph(2,6-(OMe)2)

13-24
Me
Me
H
F
F
H
H
Ph(2-NO2)

13-25
Me
Me
H
F
F
H
H
Ph(2-SMe)

13-26
Me
Me
H
H
H
Cl
H
Ph(2-F)

13-27
Me
Me
H
H
H
Cl
H
Ph(2,6-F2)

13-28
Me
Me
H
H
H
Cl
H
Ph(2-Cl)

13-29
Me
Me
H
H
H
Cl
H
Ph(2-Me)

13-30
Me
Me
H
H
H
Cl
H
Ph(2-CF3)

13-31
Me
Me
H
H
H
Cl
H
Ph(2-F-6-Cl)

13-32
Me
Me
H
H
H
Me
H
Ph(2-F)

13-33
Me
Me
H
H
H
Me
H
Ph(2,6-F2)
133-135

13-34
Me
Me
H
H
H
Me
H
Ph(2-Cl)

13-35
Me
Me
H
H
H
Me
H
Ph(2-Me)

13-36
Me
Me
H
H
H
Me
H
Ph(2-CF3)

13-37
Me
Me
H
H
H
Me
H
Ph(2-F-6-Cl)

13-38
Me
Me
H
F
F
Cl
H
Ph(2-F)

13-39
Me
Me
H
F
F
Cl
H
Ph(2,6-F2)

13-40
Me
Me
H
F
F
Cl
H
Ph(2-Cl)

13-41
Me
Me
H
F
F
Cl
H
Ph(2-Me)

13-42
Me
Me
H
F
F
Cl
H
Ph(2-CF3)

13-43
Me
Me
H
F
F
Cl
H
Ph(2-F-6-Cl)

13-44
Me
Me
H
F
F
Me
H
Ph(2-F)
105-108

13-45
Me
Me
H
F
F
Me
H
Ph(2,6-F2)
178-180

13-46
Me
Me
H
F
F
Me
H
Ph(2-Cl)

13-47
Me
Me
H
F
F
Me
H
Ph(2-Me)

13-48
Me
Me
H
F
F
Me
H
Ph(2-CF3)

13-49
Me
Me
H
F
F
Me
H
Ph(2-F-6-Cl)

13-50
Me
Me
H
H
H
H
Me
Ph(2-F)

13-51
Me
Me
H
H
H
H
Me
Ph(2,6-F2)

13-52
Me
Me
H
H
H
H
Me
Ph(2-Cl)

13-53
Me
Me
H
H
H
H
Me
Ph(2-Me)

13-54
Me
Me
H
H
H
H
Me
Ph(2-CF3)

13-55
Me
Me
H
H
H
H
Me
Ph(2-F-6-Cl)

13-56
Me
Me
H
F
F
H
Me
Ph(2-F)

13-57
Me
Me
H
F
F
H
Me
Ph(2,6-F2)

13-58
Me
Me
H
F
F
H
Me
Ph(2-Cl)

13-59
Me
Me
H
F
F
H
Me
Ph(2-Me)

13-60
Me
Me
H
F
F
H
Me
Ph(2-CF3)

13-61
Me
Me
H
F
F
H
Me
Ph(2-F-6-Cl)

13-62
Me
Me
H
Me
Me
Me
H
Ph(2-F)

13-63
Me
Me
H
Me
Me
Me
H
Ph(2,6-F2)

13-64
Me
Me
H
Me
Me
Me
H
Ph(2-Cl)

13-65
Me
Me
H
Me
Me
Me
H
Ph(2-Me)

13-66
Me
Me
H
Me
Me
Me
H
Ph(2-CF3)

13-67
Me
Me
H
Me
Me
Me
H
Ph(2-F-6-Cl)

13-68
Me
Me
H
Me
Me
H
Me
Ph(2-F)

13-69
Me
Me
H
Me
Me
H
Me
Ph(2,6-F2)

13-70
Me
Me
H
Me
Me
H
Me
Ph(2-Cl)

13-71
Me
Me
H
Me
Me
H
Me
Ph(2-Me)

13-72
Me
Me
H
Me
Me
H
Me
Ph(2-CF3)

13-73
Me
Me
H
Me
Me
H
Me
Ph(2-F-6-Cl)

13-74
Me
Me
H
H
H
H
Cl
Ph(2-F)

13-75
Me
Me
H
H
H
H
Cl
Ph(2,6-F2)

13-76
Me
Me
H
H
H
H
Cl
Ph(2-Cl)

13-77
Me
Me
H
H
H
H
Cl
Ph(2-Me)

13-78
Me
Me
H
H
H
H
Cl
Ph(2-CF3)

13-79
Me
Me
H
H
H
H
Cl
Ph(2-F-6-Cl)

13-80
Me
Me
H
F
F
H
Cl
Ph(2-F)

13-81
Me
Me
H
F
F
H
Cl
Ph(2,6-F2)

13-82
Me
Me
H
F
F
H
Cl
Ph(2-Cl)

13-83
Me
Me
H
F
F
H
Cl
Ph(2-Me)

13-84
Me
Me
H
F
F
H
Cl
Ph(2-CF3)

13-85
Me
Me
H
F
F
H
Cl
Ph(2-F-6-Cl)

13-86
Me
Me
H
Me
Me
Cl
H
Ph(2-F)

13-87
Me
Me
H
Me
Me
Cl
H
Ph(2,6-F2)

13-88
Me
Me
H
Me
Me
Cl
H
Ph(2-Cl)

13-89
Me
Me
H
Me
Me
Cl
H
Ph(2-Me)

13-90
Me
Me
H
Me
Me
Cl
H
Ph(2-CF3)

13-91
Me
Me
H
Me
Me
Cl
H
Ph(2-F-6-Cl)

13-92
Me
Me
H
Me
Me
H
Cl
Ph(2-F)

13-93
Me
Me
H
Me
Me
H
Cl
Ph(2,6-F2)

13-94
Me
Me
H
Me
Me
H
Cl
Ph(2-Cl)

13-95
Me
Me
H
Me
Me
H
Cl
Ph(2-Me)

13-96
Me
Me
H
Me
Me
H
Cl
Ph(2-CF3)

13-97
Me
Me
H
Me
Me
H
Cl
Ph(2-F-6-Cl)

[0253]

14

TABLE 14

Physical

Compound

properties

No.
R1
R2
R3
X1
X2
B

14-1
Me
Me
H
H
H
Ph

14-2
Me
Me
H
H
H
Ph(2-Cl)

14-3
Me
Me
H
H
H
Ph(4-Cl)

14-4
Me
Me
H
H
H
Ph(2-CF3)

14-5
Me
Me
H
H
H
Ph(4-CF3)

14-6
Me
Me
H
H
H
Ph(2-F)

14-7
Me
Me
H
H
H
Ph(2,6-F2)

14-8
Me
Me
H
H
H
Ph(2-OCF3)

14-9
Me
Me
H
H
H
Ph(2-OCHF2)

14-10
Me
Me
H
H
H
Ph(2-OMe)

14-11
Me
Me
H
H
H
Ph(2,6-(OMe)2)

14-12
Me
Me
H
F
F
Ph(2-NO2)

14-13
Me
Me
H
F
F
Ph

14-14
Me
Me
H
F
F
Ph(2-Cl)

14-15
Me
Me
H
F
F
Ph(4-Cl)

14-16
Me
Me
H
F
F
Ph(2-CF3)

14-17
Me
Me
H
F
F
Ph(4-CF3)

14-18
Me
Me
H
F
F
Ph(2-F)

14-19
Me
Me
H
F
F
Ph(2,6-F2)

14-20
Me
Me
H
F
F
Ph(2-OCF3)

14-21
Me
Me
H
F
F
Ph(2-OCHF2)

14-22
Me
Me
H
F
F
Ph(2-OMe)

14-23
Me
Me
H
F
F
Ph(2,6-(OMe)2)

14-24
Me
Me
H
F
F
Ph(2-NO2)

14-25
Me
Me
H
F
F
Ph(2-SMe)

[0254]

15

TABLE 15

Com-

Physical

pound

properties

No.
R1
R2
R3
X1
X2
X3
X4
B
(mp ° C.)

15-1
Me
Me
H
H
H
Me
H
Ph(2-F)

15-2
Me
Me
H
H
H
Me
H
Ph(2,6-F2)

15-3
Me
Me
H
H
H
Me
H
Ph(2-Cl)

15-4
Me
Me
H
H
H
Me
H
Ph(2-Me)

15-5
Me
Me
H
H
H
Me
H
Ph(2-CF3)

15-6
Me
Me
H
H
H
Me
H
Ph(2-F-6-Cl)

15-7
Me
Me
H
H
H
H
Me
Ph(2-F)

15-8
Me
Me
H
H
H
H
Me
Ph(2,6-F2)

15-9
Me
Me
H
H
H
H
Me
Ph(2-Cl)

15-10
Me
Me
H
H
H
H
Me
Ph(2-Me)

15-11
Me
Me
H
H
H
H
Me
Ph(2-CF3)

15-12
Me
Me
H
H
H
H
Me
Ph(2-F-6-Cl)

15-13
Me
Me
H
Me
H
H
H
Ph(2-F)

15-14
Me
Me
H
Me
H
H
H
Ph(2,6-F2)

15-15
Me
Me
H
Me
H
H
H
Ph(2-Cl)

15-16
Me
Me
H
Me
H
H
H
Ph(2-Me)

15-17
Me
Me
H
Me
H
H
H
Ph(2-CF3)

15-18
Me
Me
H
Me
H
H
H
Ph(2-F-6-Cl)

15-19
Me
Me
H
Me
H
Me
H
Ph(2-F)

15-20
Me
Me
H
Me
H
Me
H
Ph(2,6-F2)

15-21
Me
Me
H
Me
H
Me
H
Ph(2-Cl)

15-22
Me
Me
H
Me
H
Me
H
Ph(2-Me)

15-23
Me
Me
H
Me
H
Me
H
Ph(2-CF3)

15-24
Me
Me
H
Me
H
Me
H
Ph(2-F-6-Cl)

15-25
Me
Me
H
Me
H
H
Me
Ph(2-F)

15-26
Me
Me
H
Me
H
H
Me
Ph(2,6-F2)

15-27
Me
Me
H
Me
H
H
Me
Ph(2-Cl)

15-28
Me
Me
H
Me
H
H
Me
Ph(2-Me)

15-29
Me
Me
H
Me
H
H
Me
Ph(2-CF3)

15-30
Me
Me
H
Me
H
H
Me
Ph(2-F-6-Cl)

15-31
Me
Me
H
H
Me
H
H
Ph(2-F)

15-32
Me
Me
H
H
Me
H
H
Ph(2,6-F2)

15-33
Me
Me
H
H
Me
H
H
Ph(2-Cl)

15-34
Me
Me
H
H
Me
H
H
Ph(2-Me)

15-35
Me
Me
H
H
Me
H
H
Ph(2-CF3)

15-36
Me
Me
H
H
Me
H
H
Ph(2-F-6-Cl)

15-37
Me
Me
H
H
Me
Me
H
Ph(2-F)

15-38
Me
Me
H
H
Me
Me
H
Ph(2,6-F2)

15-39
Me
Me
H
H
Me
Me
H
Ph(2-Cl)

15-40
Me
Me
H
H
Me
Me
H
Ph(2-Me)

15-41
Me
Me
H
H
Me
Me
H
Ph(2-CF3)

15-42
Me
Me
H
H
Me
Me
H
Ph(2-F-6-Cl)

15-43
Me
Me
H
H
Me
H
Me
Ph(2-F)

15-44
Me
Me
H
H
Me
H
Me
Ph(2,6-F2)

15-45
Me
Me
H
H
Me
H
Me
Ph(2-Cl)

15-46
Me
Me
H
H
Me
H
Me
Ph(2-Me)

15-47
Me
Me
H
H
Me
H
Me
Ph(2-CF3)

15-48
Me
Me
H
H
Me
H
Me
Ph(2-F-6-Cl)

15-49
Me
Me
H
H
H
Cl
H
Ph(2-F)

15-50
Me
Me
H
H
H
Cl
H
Ph(2,6-F2)

15-51
Me
Me
H
H
H
Cl
H
Ph(2-Cl)

15-52
Me
Me
H
H
H
Cl
H
Ph(2-Me)

15-53
Me
Me
H
H
H
Cl
H
Ph(2-CF3)

15-54
Me
Me
H
H
H
Cl
H
Ph(2-F-6-Cl)

15-55
Me
Me
H
H
H
H
Cl
Ph(2-F)

15-56
Me
Me
H
H
H
H
Cl
Ph(2,6-F2)

15-57
Me
Me
H
H
H
H
Cl
Ph(2-Cl)

15-58
Me
Me
H
H
H
H
Cl
Ph(2-Me)

15-59
Me
Me
H
H
H
H
Cl
Ph(2-CF3)

15-60
Me
Me
H
H
H
H
Cl
Ph(2-F-6-Cl)

15-61
Me
Me
H
Cl
H
H
H
Ph(2-F)

15-62
Me
Me
H
Cl
H
H
H
Ph(2,6-F2)

15-63
Me
Me
H
Cl
H
H
H
Ph(2-Cl)

15-64
Me
Me
H
Cl
H
H
H
Ph(2-Me)

15-65
Me
Me
H
Cl
H
H
H
Ph(2-CF3)

15-66
Me
Me
H
Cl
H
H
H
Ph(2-F-6-Cl)

15-67
Me
Me
H
Me
H
Cl
H
Ph(2-F)

15-68
Me
Me
H
Me
H
Cl
H
Ph(2,6-F2)

15-69
Me
Me
H
Me
H
Cl
H
Ph(2-Cl)

15-70
Me
Me
H
Me
H
Cl
H
Ph(2-Me)

15-71
Me
Me
H
Me
H
Cl
H
Ph(2-CF3)

15-72
Me
Me
H
Me
H
Cl
H
Ph(2-F-6-Cl)

15-73
Me
Me
H
Me
H
H
Cl
Ph(2-F)

15-74
Me
Me
H
Me
H
H
Cl
Ph(2,6-F2)

15-75
Me
Me
H
Me
H
H
Cl
Ph(2-Cl)

15-76
Me
Me
H
Me
H
H
Cl
Ph(2-Me)

15-77
Me
Me
H
Me
H
H
Cl
ph(2-CF3)

15-78
Me
Me
H
Me
H
H
Cl
ph(2-F-6-Cl)

15-79
Me
Me
H
H
Cl
H
H
Ph(2-F)

15-80
Me
Me
H
H
Cl
H
H
Ph(2,6-F2)

15-81
Me
Me
H
H
Cl
H
H
Ph(2-Cl)

15-82
Me
Me
H
H
Cl
H
H
Ph(2-Me)

15-83
Me
Me
H
H
Cl
H
H
Ph(2-CF3)

15-84
Me
Me
H
H
Cl
H
H
Ph(2-F-6-Cl)

15-85
Me
Me
H
H
Me
Cl
H
Ph(2-F)

15-86
Me
Me
H
H
Me
Cl
H
Ph(2,6-F2)

15-87
Me
Me
H
H
Me
Cl
H
Ph(2-Cl)

15-88
Me
Me
H
H
Me
Cl
H
Ph(2-Me)

15-89
Me
Me
H
H
Me
Cl
H
Ph(2-CF3)

15-90
Me
Me
H
H
Me
Cl
H
Ph(2-F-6-Cl)

15-91
Me
Me
H
H
Me
H
Cl
Ph(2-F)

15-92
Me
Me
H
H
Me
H
Cl
Ph(2,6-F2)

15-93
Me
Me
H
H
Me
H
Cl
Ph(2-Cl)

15-94
Me
Me
H
H
Me
H
Cl
Ph(2-Me)

15-95
Me
Me
H
H
Me
H
Cl
Ph(2-CF3)

15-96
Me
Me
H
H
Me
H
Cl
Ph(2-F-6-Cl)

[0255]

16

TABLE 16

Physical

Compound

properties

No.
R1
R2
R3
X1
X2
X3
X4
B
(mp ° C.)

16-1
Me
Me
H
H
F
Me
H
Ph(2-F)

16-2
Me
Me
H
H
F
Me
H
Ph(2,6-F2)

16-3
Me
Me
H
H
F
Me
H
Ph(2-Cl)

16-4
Me
Me
H
H
F
Me
H
Ph(2-Me)

16-5
Me
Me
H
H
F
Me
H
Ph(2-CF3)

16-6
Me
Me
H
H
F
Me
H
Ph(2-F-6-Cl)

16-7
Me
Me
H
H
F
H
Me
Ph(2-F)

16-8
Me
Me
H
H
F
H
Me
Ph(2,6-F2)

16-9
Me
Me
H
H
F
H
Me
Ph(2-Cl)

16-10
Me
Me
H
H
F
H
Me
Ph(2-Me)

16-11
Me
Me
H
H
F
H
Me
Ph(2-CF3)

16-12
Me
Me
H
H
F
H
Me
Ph(2-F-6-Cl)

16-13
Me
Me
H
F
H
H
H
Ph(2-F)

16-14
Me
Me
H
F
H
H
H
Ph(2,6-F2)

16-15
Me
Me
H
F
H
H
H
Ph(2-Cl)

16-16
Me
Me
H
F
H
H
H
Ph(2-Me)

16-17
Me
Me
H
F
H
H
H
Ph(2-CF3)

16-18
Me
Me
H
F
H
H
H
Ph(2-F-6-Cl)

16-19
Me
Me
H
F
H
Me
H
Ph(2-F)

16-20
Me
Me
H
F
H
Me
H
Ph(2,6-F2)

16-21
Me
Me
H
F
H
Me
H
Ph(2-Cl)

16-22
Me
Me
H
F
H
Me
H
Ph(2-Me)

16-23
Me
Me
H
F
H
Me
H
Ph(2-CF3)

16-24
Me
Me
H
F
H
Me
H
Ph(2-F-6-Cl)

16-25
Me
Me
H
F
H
H
Me
Ph(2-F)

16-26
Me
Me
H
F
H
H
Me
Ph(2,6-F2)

16-27
Me
Me
H
F
H
H
Me
Ph(2-Cl)

16-28
Me
Me
H
F
H
H
Me
Ph(2-Me)

16-29
Me
Me
H
F
H
H
Me
Ph(2-CF3)

16-30
Me
Me
H
F
H
H
Me
Ph(2-F-6-Cl)

16-31
Me
Me
H
F
F
H
H
Ph(2-F)

16-32
Me
Me
H
F
F
H
H
Ph(2,6-F2)
125-128

16-33
Me
Me
H
F
F
H
H
Ph(2-Cl)

16-34
Me
Me
H
F
F
H
H
Ph(2-Me)

16-35
Me
Me
H
F
F
H
H
Ph(2-CF3)

16-36
Me
Me
H
F
F
H
H
Ph(2-F-6-Cl)

16-37
Me
Me
H
F
F
Me
H
Ph(2-F)
110-112

16-38
Me
Me
H
F
F
Me
H
Ph(2,6-F2)
128-130

16-39
Me
Me
H
F
F
Me
H
Ph(2-Cl)

16-40
Me
Me
H
F
F
Me
H
Ph(2-Me)

16-41
Me
Me
H
F
F
Me
H
Ph(2-CF3)

16-42
Me
Me
H
F
F
Me
H
Ph(2-F-6-Cl)

16-43
Me
Me
H
F
F
H
Me
Ph(2-F)

16-44
Me
Me
H
F
F
H
Me
Ph(2,6-F2)

16-45
Me
Me
H
F
F
H
Me
Ph(2-Cl)

16-46
Me
Me
H
F
F
H
Me
Ph(2-Me)

16-47
Me
Me
H
F
F
H
Me
Ph(2-CF3)

16-48
Me
Me
H
F
F
H
Me
Ph(2-F-6-Cl)

16-49
Me
Me
H
H
F
Cl
H
Ph(2-F)

16-50
Me
Me
H
H
F
Cl
H
Ph(2,6-F2)

16-51
Me
Me
H
H
F
Cl
H
Ph(2-Cl)

16-52
Me
Me
H
H
F
Cl
H
Ph(2-Me)

16-53
Me
Me
H
H
F
Cl
H
Ph(2-CF3)

16-54
Me
Me
H
H
F
Cl
H
Ph(2-F-6-Cl)

16-55
Me
Me
H
H
F
H
Cl
Ph(2-F)

16-56
Me
Me
H
H
F
H
Cl
Ph(2,6-F2)

16-57
Me
Me
H
H
F
H
Cl
Ph(2-Cl)

16-58
Me
Me
H
H
F
H
Cl
Ph(2-Me)

16-59
Me
Me
H
H
F
H
Cl
Ph(2-CF3)

16-60
Me
Me
H
H
F
H
Cl
Ph(2-F-6-Cl)

16-61
Me
Me
H
F
H
Cl
H
Ph(2-F)

16-62
Me
Me
H
F
H
Cl
H
Ph(2,6-F2)

16-63
Me
Me
H
F
H
Cl
H
Ph(2-Cl)

16-64
Me
Me
H
F
H
Cl
H
Ph(2-Me)

16-65
Me
Me
H
F
H
Cl
H
Ph(2-CF3)

16-66
Me
Me
H
F
H
Cl
H
Ph(2-F-6-Cl)

16-67
Me
Me
H
F
H
H
Cl
Ph(2-F)

16-68
Me
Me
H
F
H
H
Cl
Ph(2,6-F2)

16-69
Me
Me
H
F
H
H
Cl
Ph(2-Cl)

16-70
Me
Me
H
F
H
H
Cl
Ph(2-Me)

16-71
Me
Me
H
F
H
H
Cl
Ph(2-CF3)

16-72
Me
Me
H
F
H
H
Cl
Ph(2-F-6-Cl)

16-73
Me
Me
H
F
F
Cl
H
Ph(2-F)

16-74
Me
Me
H
F
F
Cl
H
Ph(2,6-F2)

16-75
Me
Me
H
F
F
Cl
H
Ph(2-Cl)

16-76
Me
Me
H
F
F
Cl
H
Ph(2-Me)

16-77
Me
Me
H
F
F
Cl
H
Ph(2-CF3)

16-78
Me
Me
H
F
F
Cl
H
Ph(2-F-6-Cl)

16-79
Me
Me
H
F
F
H
Cl
Ph(2-F)

16-80
Me
Me
H
F
F
H
Cl
Ph(2,6-F2)

16-81
Me
Me
H
F
F
H
Cl
Ph(2-Cl)

16-82
Me
Me
H
F
F
H
Cl
Ph(2-Me)

16-83
Me
Me
H
F
F
H
Cl
Ph(2-CF3)

16-84
Me
Me
H
F
F
H
Cl
Ph(2-F-6-Cl)

[0256]

17

TABLE 17

Physical

Compound

properties

No.
R1
R2
R3
X1
X2
X3
X4
B
(mp ° C.)

17-1
Me
Me
H
F
H
H
H
Ph(2-F)

17-2
Me
Me
H
F
H
H
H
Ph(2,6-F2)

17-3
Me
Me
H
F
H
H
H
Ph(2-Cl)

17-4
Me
Me
H
F
H
H
H
Ph(2-Me)

17-5
Me
Me
H
F
H
H
H
Ph(2-CF3)

17-6
Me
Me
H
F
H
H
H
Ph(2-F-6-Cl)

17-7
Me
Me
H
F
H
Me
H
Ph(2-F)

17-8
Me
Me
H
F
H
Me
H
Ph(2,6-F2)

17-9
Me
Me
H
F
H
Me
H
Ph(2-Cl)

17-10
Me
Me
H
F
H
Me
H
Ph(2-Me)

17-11
Me
Me
H
F
H
Me
H
Ph(2-CF3)

17-12
Me
Me
H
F
H
Me
H
Ph(2-F-6-Cl)

17-13
Me
Me
H
F
Cl
H
H
Ph(2-F)

17-14
Me
Me
H
F
Cl
H
H
Ph(2,6-F2)

17-15
Me
Me
H
F
Cl
H
H
Ph(2-Cl)

17-16
Me
Me
H
F
Cl
H
H
Ph(2-Me)

17-17
Me
Me
H
F
Cl
H
H
Ph(2-CF3)

17-18
Me
Me
H
F
Cl
H
H
Ph(2-F-6-Cl)

17-19
Me
Me
H
F
Cl
Me
H
Ph(2-F)

17-20
Me
Me
H
F
Cl
Me
H
Ph(2,6-F2)

17-21
Me
Me
H
F
Cl
Me
H
Ph(2-Cl)

17-22
Me
Me
H
F
Cl
Me
H
Ph(2-Me)

17-23
Me
Me
H
F
Cl
Me
H
Ph(2-CF3)

17-24
Me
Me
H
F
Cl
Me
H
Ph(2-F-6-Cl)

17-25
Me
Me
H
H
F
H
H
Ph(2-F)

17-26
Me
Me
H
H
F
H
H
Ph(2,6-F2)

17-27
Me
Me
H
H
F
H
H
Ph(2-Cl)

17-28
Me
Me
H
H
F
H
H
Ph(2-Me)

17-29
Me
Me
H
H
F
H
H
Ph(2-CF3)

17-30
Me
Me
H
H
F
H
H
Ph(2-F-6-Cl)

17-31
Me
Me
H
H
F
Me
H
Ph(2-F)

17-32
Me
Me
H
H
F
Me
H
Ph(2,6-F2)

17-33
Me
Me
H
H
F
Me
H
Ph(2-Cl)

17-34
Me
Me
H
H
F
Me
H
Ph(2-Me)

17-35
Me
Me
H
H
F
Me
H
Ph(2-CF3)

17-36
Me
Me
H
H
F
Me
H
Ph(2-F-6-Cl)

17-37
Me
Me
H
Cl
F
H
H
Ph(2-F)

17-38
Me
Me
H
Cl
F
H
H
Ph(2,6-F2)

17-39
Me
Me
H
Cl
F
H
H
Ph(2-Cl)

17-40
Me
Me
H
Cl
F
H
H
Ph(2-Me)

17-41
Me
Me
H
Cl
F
H
H
Ph(2-CF3)

17-42
Me
Me
H
Cl
F
H
H
Ph(2-F-6-Cl)

17-43
Me
Me
H
Cl
F
Me
H
Ph(2-F)

17-44
Me
Me
H
Cl
F
Me
H
Ph(2,6-F2)

17-45
Me
Me
H
Cl
F
Me
H
Ph(2-Cl)

17-46
Me
Me
H
Cl
F
Me
H
Ph(2-Me)

17-47
Me
Me
H
Cl
F
Me
H
Ph(2-CF3)

17-48
Me
Me
H
Cl
F
Me
H
Ph(2-F-6-Cl)

17-49
Me
Me
H
F
H
Cl
H
Ph(2-F)

17-50
Me
Me
H
F
H
Cl
H
Ph(2,6-F2)

17-51
Me
Me
H
F
H
Cl
H
Ph(2-Cl)

17-52
Me
Me
H
F
H
Cl
H
Ph(2-Me)

17-53
Me
Me
H
F
H
Cl
H
Ph(2-CF3)

17-54
Me
Me
H
F
H
Cl
H
Ph(2-F-6-Cl)

17-55
Me
Me
H
F
Cl
Cl
H
Ph(2-F)

17-56
Me
Me
H
F
Cl
Cl
H
Ph(2,6-F2)

17-57
Me
Me
H
F
Cl
Cl
H
Ph(2-Cl)

17-58
Me
Me
H
F
Cl
Cl
H
Ph(2-Me)

17-59
Me
Me
H
F
Cl
Cl
H
Ph(2-CF3)

17-60
Me
Me
H
F
Cl
Cl
H
Ph(2-F-6-Cl)

17-61
Me
Me
H
H
F
Cl
H
Ph(2-F)

17-62
Me
Me
H
H
F
Cl
H
Ph(2,6-F2)

17-63
Me
Me
H
H
F
Cl
H
Ph(2-Cl)

17-64
Me
Me
H
H
F
Cl
H
Ph(2-Me)

17-65
Me
Me
H
H
F
Cl
H
Ph(2-CF3)

17-66
Me
Me
H
H
F
Cl
H
Ph(2-F-6-Cl)

17-67
Me
Me
H
Cl
F
Cl
H
Ph(2-F)

17-68
Me
Me
H
Cl
F
Cl
H
Ph(2,6-F2)

17-69
Me
Me
H
Cl
F
Cl
H
Ph(2-Cl)

17-70
Me
Me
H
Cl
F
Cl
H
Ph(2-Me)

17-71
Me
Me
H
Cl
F
Cl
H
Ph(2-CF3)

17-72
Me
Me
H
Cl
F
Cl
H
Ph(2-F-6-Cl)

[0257]

18

TABLE 18

Physical

Compound

properties

No.
R1
R2
R3
X1
X2
X3
X4
B
(mp ° C.)

18-1
Me
Me
H
H
H
H
H
Ph(2-F)

18-2
Me
Me
H
H
H
H
H
Ph(2,6-F2)

18-3
Me
Me
H
H
H
H
H
Ph(2-Cl)

18-4
Me
Me
H
H
H
H
H
Ph(2-Me)

18-5
Me
Me
H
H
H
H
H
Ph(2-CF3)

18-6
Me
Me
H
H
H
H
H
Ph(2-F-6-Cl)

18-7
Me
Me
H
H
H
Me
H
Ph(2-F)

18-8
Me
Me
H
H
H
Me
H
Ph(2,6-F2)

18-9
Me
Me
H
H
H
Me
H
Ph(2-Cl)

18-10
Me
Me
H
H
H
Me
H
Ph(2-Me)

18-11
Me
Me
H
H
H
Me
H
Ph(2-CF3)

18-12
Me
Me
H
H
H
Me
H
Ph(2-F-6-Cl)

18-13
Me
Me
H
F
H
H
H
Ph(2-F)

18-14
Me
Me
H
F
H
H
H
Ph(2,6-F2)

18-15
Me
Me
H
F
H
H
H
Ph(2-Cl)

18-16
Me
Me
H
F
H
H
H
Ph(2-Me)

18-17
Me
Me
H
F
H
H
H
Ph(2-CF3)

18-18
Me
Me
H
F
H
H
H
Ph(2-F-6-Cl)

18-19
Me
Me
H
F
H
Me
H
Ph(2-F)

18-20
Me
Me
H
F
H
Me
H
Ph(2,6-F2)

18-21
Me
Me
H
F
H
Me
H
Ph(2-Cl)

18-22
Me
Me
H
F
H
Me
H
Ph(2-Me)

18-23
Me
Me
H
F
H
Me
H
Ph(2-CF3)

18-24
Me
Me
H
F
H
Me
H
Ph(2-F-6-Cl)

18-25
Me
Me
H
F
H
H
Me
Ph(2-F)

18-26
Me
Me
H
F
H
H
Me
Ph(2,6-F2)

18-27
Me
Me
H
F
H
H
Me
Ph(2-Cl)

18-28
Me
Me
H
F
H
H
Me
Ph(2-Me)

18-29
Me
Me
H
F
H
H
Me
Ph(2-CF3)

18-30
Me
Me
H
F
H
H
Me
Ph(2-F-6-Cl)

18-31
Me
Me
H
F
F
H
H
Ph(2-F)

18-32
Me
Me
H
F
F
H
H
Ph(2,6-F2)

18-33
Me
Me
H
F
F
H
H
Ph(2-Cl)

18-34
Me
Me
H
F
F
H
H
Ph(2-Me)

18-35
Me
Me
H
F
F
H
H
Ph(2-CF3)

18-36
Me
Me
H
F
F
H
H
Ph(2-F-6-Cl)

18-37
Me
Me
H
F
F
Me
H
Ph(2-F)

18-38
Me
Me
H
F
F
Me
H
Ph(2,6-F2)

18-39
Me
Me
H
F
F
Me
H
Ph(2-Cl)

18-40
Me
Me
H
F
F
Me
H
Ph(2-Me)

18-41
Me
Me
H
F
F
Me
H
Ph(2-CF3)

18-42
Me
Me
H
F
F
Me
H
Ph(2-F-6-Cl)

18-43
Me
Me
H
F
F
H
Me
Ph(2-F)

18-44
Me
Me
H
F
F
H
Me
Ph(2,6-F2)

18-45
Me
Me
H
F
F
H
Me
Ph(2-Cl)

18-46
Me
Me
H
F
F
H
Me
Ph(2-Me)

18-47
Me
Me
H
F
F
H
Me
Ph(2-CF3)

18-48
Me
Me
H
F
F
H
Me
Ph(2-F-6-Cl)

[0258]

19

TABLE 19

Physical

Compound

properties

No.
R1
R2
R3
X1
X2
B
(mp ° C.)

19-1
Me
Me
H
H
H
Ph(2-F)

19-2
Me
Me
H
H
H
Ph(2,6-F2)

19-3
Me
Me
H
H
H
Ph(2-Cl)

19-4
Me
Me
H
H
H
Ph(2-Me)

19-5
Me
Me
H
H
H
Ph(2-CF3)

19-6
Me
Me
H
H
H
Ph(2-F-6-Cl)

19-7
Me
Me
H
H
Cl
Ph(2-F)

19-8
Me
Me
H
H
Cl
Ph(2,6-F2)

19-9
Me
Me
H
H
Cl
Ph(2-Cl)

19-10
Me
Me
H
H
Cl
Ph(2-Me)

19-11
Me
Me
H
H
Cl
Ph(2-CF3)

19-12
Me
Me
H
H
Cl
Ph(2-F-6-Cl)

19-13
Me
Me
H
H
Me
Ph(2-F)

19-14
Me
Me
H
H
Me
Ph(2,6-F2)

19-15
Me
Me
H
H
Me
Ph(2-Cl)

19-16
Me
Me
H
H
Me
Ph(2-Me)

19-17
Me
Me
H
H
Me
Ph(2-CF3)

19-18
Me
Me
H
H
Me
Ph(2-F-6-Cl)

19-19
Me
Me
H
H
OMe
Ph(2-F)

19-20
Me
Me
H
H
OMe
Ph(2,6-F2)

19-21
Me
Me
H
H
OMe
Ph(2-Cl)

19-22
Me
Me
H
H
OMe
Ph(2-Me)

19-23
Me
Me
H
H
OMe
Ph(2-CF3)

19-24
Me
Me
H
H
OMe
Ph(2-F-6-Cl)

19-25
Me
Me
H
F
H
Ph(2-F)

19-26
Me
Me
H
F
H
Ph(2,6-F2)

19-27
Me
Me
H
F
H
Ph(2-Cl)

19-28
Me
Me
H
F
H
Ph(2-Me)

19-29
Me
Me
H
F
H
Ph(2-CF3)

19-30
Me
Me
H
F
H
Ph(2-F-6-Cl)

19-31
Me
Me
H
F
Cl
Ph(2-F)

19-32
Me
Me
H
F
Cl
Ph(2,6-F2)

19-33
Me
Me
H
F
Cl
Ph(2-Cl)

19-34
Me
Me
H
F
Cl
Ph(2-Me)

19-35
Me
Me
H
F
Cl
Ph(2-CF3)

19-36
Me
Me
H
F
Cl
Ph(2-F-6-Cl)

19-37
Me
Me
H
F
Me
Ph(2-F)

19-38
Me
Me
H
F
Me
Ph(2,6-F2)

19-39
Me
Me
H
F
Me
Ph(2-Cl)

19-40
Me
Me
H
F
Me
Ph(2-Me)

19-41
Me
Me
H
F
Me
Ph(2-CF3)

19-42
Me
Me
H
F
Me
Ph(2-F-6-Cl)

19-43
Me
Me
H
F
OMe
Ph(2-F)

19-44
Me
Me
H
F
OMe
Ph(2,6-F2)

19-45
Me
Me
H
F
OMe
Ph(2-Cl)

19-46
Me
Me
H
F
OMe
Ph(2-Me)

19-47
Me
Me
H
F
OMe
Ph(2-CF3)

19-48
Me
Me
H
F
OMe
Ph(2-F-6-Cl)

19-49
Me
Me
H
H
Br
Ph(2-F)

19-50
Me
Me
H
H
Br
Ph(2,6-F2)

19-51
Me
Me
H
H
Br
Ph(2-Cl)

19-52
Me
Me
H
H
Br
Ph(2-Me)

19-53
Me
Me
H
H
Br
Ph(2-CF3)

19-54
Me
Me
H
H
Br
Ph(2-F-6-Cl)

19-55
Me
Me
H
H
CF3
Ph(2-F)

19-56
Me
Me
H
H
CF3
Ph(2,6-F2)

19-57
Me
Me
H
H
CF3
Ph(2-Cl)

19-58
Me
Me
H
H
CF3
Ph(2-Me)

19-59
Me
Me
H
H
CF3
Ph(2-CF3)

19-60
Me
Me
H
H
CF3
Ph(2-F-6-Cl)

19-61
Me
Me
H
H
OCF3
Ph(2-F)

19-62
Me
Me
H
H
OCF3
Ph(2,6-F2)

19-63
Me
Me
H
H
OCF3
Ph(2-Cl)

19-64
Me
Me
H
H
OCF3
Ph(2-Me)

19-65
Me
Me
H
H
OCF3
Ph(2-CF3)

19-66
Me
Me
H
H
OCF3
Ph(2-F-6-Cl)

19-67
Me
Me
H
H
OCH2CF3
Ph(2-F)

19-68
Me
Me
H
H
OCH2CF3
Ph(2,6-F2)

19-69
Me
Me
H
H
OCH2CF3
Ph(2-Cl)

19-70
Me
Me
H
H
OCH2CF3
Ph(2-Me)

19-71
Me
Me
H
H
OCH2CF3
Ph(2-CF3)

19-72
Me
Me
H
H
OCH2CF3
Ph(2-F-6-Cl)

19-73
Me
Me
H
H
OCHF2
Ph(2-F)

19-74
Me
Me
H
H
OCHF2
Ph(2,6-F2)

19-75
Me
Me
H
H
OCHF2
Ph(2-Cl)

19-76
Me
Me
H
H
OCHF2
Ph(2-Me)

19-77
Me
Me
H
H
OCHF2
Ph(2-CF3)

19-78
Me
Me
H
H
OCHF2
Ph(2-F-6-Cl)

19-79
Me
Me
H
F
Br
Ph(2-F)

19-80
Me
Me
H
F
Br
Ph(2,6-F2)

19-81
Me
Me
H
F
Br
Ph(2-Cl)

19-82
Me
Me
H
F
Br
Ph(2-Me)

19-83
Me
Me
H
F
Br
Ph(2-CF3)

19-84
Me
Me
H
F
Br
Ph(2-F-6-Cl)

19-85
Me
Me
H
F
CF3
Ph(2-F)

19-86
Me
Me
H
F
CF3
Ph(2,6-F2)

19-87
Me
Me
H
F
CF3
Ph(2-Cl)

19-88
Me
Me
H
F
CF3
Ph(2-Me)

19-89
Me
Me
H
F
CF3
Ph(2-CF3)

19-90
Me
Me
H
F
CF3
Ph(2-F-6-Cl)

19-91
Me
Me
H
F
OCF3
Ph(2-F)

19-92
Me
Me
H
F
OCF3
Ph(2,6-F2)

19-93
Me
Me
H
F
OCF3
Ph(2-Cl)

19-94
Me
Me
H
F
OCF3
Ph(2-Me)

19-95
Me
Me
H
F
OCF3
Ph(2-CF3)

19-96
Me
Me
H
F
OCF3
Ph(2-F-6-Cl)

19-97
Me
Me
H
F
OCH2CF3
Ph(2-F)

19-98
Me
Me
H
F
OCH2CF3
Ph(2,6-F2)

19-99
Me
Me
H
F
OCH2CF3
Ph(2-Cl)

19-100
Me
Me
H
F
OCH2CF3
Ph(2-Me)

19-101
Me
Me
H
F
OCH2CF3
Ph(2-CF3)

19-102
Me
Me
H
F
OCH2CF3
Ph(2-F-6-Cl)

19-103
Me
Me
H
F
OCHF2
Ph(2-F)

19-104
Me
Me
H
F
OCHF2
Ph(2,6-F2)

19-105
Me
Me
H
F
OCHF2
Ph(2-Cl)

19-106
Me
Me
H
F
OCHF2
Ph(2-Me)

19-107
Me
Me
H
F
OCHF2
Ph(2-CF3)

19-108
Me
Me
H
F
OCHF2
Ph(2-F-6-Cl)

[0259]

20

TABLE 20

Physical

Compound

properties

No.
R1
R2
R3
X1
X2
B
(mp ° C.)

20-1
Me
Me
H
H
H
Ph(2-F)

20-2
Me
Me
H
H
H
Ph(2,6-F2)

20-3
Me
Me
H
H
H
Ph(2-Cl)

20-4
Me
Me
H
H
H
Ph(2-Me)

20-5
Me
Me
H
H
H
Ph(2-CF3)

20-6
Me
Me
H
H
H
Ph(2-F-6-Cl)

20-7
Me
Me
H
H
Cl
Ph(2-F)

20-8
Me
Me
H
H
Cl
Ph(2,6-F2)

20-9
Me
Me
H
H
Cl
Ph(2-Cl)

20-10
Me
Me
H
H
Cl
Ph(2-Me)

20-11
Me
Me
H
H
Cl
Ph(2-CF3)

20-12
Me
Me
H
H
Cl
Ph(2-F-6-Cl)

20-13
Me
Me
H
H
Me
Ph(2-F)

20-14
Me
Me
H
H
Me
Ph(2,6-F2)

20-15
Me
Me
H
H
Me
Ph(2-Cl)

20-16
Me
Me
H
H
Me
Ph(2-Me)

20-17
Me
Me
H
H
Me
Ph(2-CF3)

20-18
Me
Me
H
H
Me
Ph(2-F-6-Cl)

20-19
Me
Me
H
H
OMe
Ph(2-F)

20-20
Me
Me
H
H
OMe
Ph(2,6-F2)

20-21
Me
Me
H
H
OMe
Ph(2-Cl)

20-22
Me
Me
H
H
OMe
Ph(2-Me)

20-23
Me
Me
H
H
OMe
Ph(2-CF3)

20-24
Me
Me
H
H
OMe
Ph(2-F-6-Cl)

20-25
Me
Me
H
F
H
Ph(2-F)

20-26
Me
Me
H
F
H
Ph(2,6-F2)

20-27
Me
Me
H
F
H
Ph(2-Cl)

20-28
Me
Me
H
F
H
Ph(2-Me)

20-29
Me
Me
H
F
H
Ph(2-CF3)

20-30
Me
Me
H
F
H
Ph(2-F-6-Cl)

20-31
Me
Me
H
F
Cl
Ph(2-F)

20-32
Me
Me
H
F
Cl
Ph(2,6-F2)

20-33
Me
Me
H
F
Cl
Ph(2-Cl)

20-34
Me
Me
H
F
Cl
Ph(2-Me)

20-35
Me
Me
H
F
Cl
Ph(2-CF3)

20-36
Me
Me
H
F
Cl
Ph(2-F-6-Cl)

20-37
Me
Me
H
F
Me
Ph(2-F)

20-38
Me
Me
H
F
Me
Ph(2,6-F2)

20-39
Me
Me
H
F
Me
Ph(2-Cl)

20-40
Me
Me
H
F
Me
Ph(2-Me)

20-41
Me
Me
H
F
Me
Ph(2-CF3)

20-42
Me
Me
H
F
Me
Ph(2-F-6-Cl)

20-43
Me
Me
H
F
OMe
Ph(2-F)

20-44
Me
Me
H
F
OMe
Ph(2,6-F2)

20-45
Me
Me
H
F
OMe
Ph(2-Cl)

20-46
Me
Me
H
F
OMe
Ph(2-Me)

20-47
Me
Me
H
F
OMe
Ph(2-CF3)

20-48
Me
Me
H
F
OMe
Ph(2-F-6-Cl)

20-49
Me
Me
H
H
Br
Ph(2-F)

20-50
Me
Me
H
H
Br
Ph(2,6-F2)

20-51
Me
Me
H
H
Br
Ph(2-Cl)

20-52
Me
Me
H
H
Br
Ph(2-Me)

20-53
Me
Me
H
H
Br
Ph(2-CF3)

20-54
Me
Me
H
H
Br
Ph(2-F-6-Cl)

20-55
Me
Me
H
H
CF3
Ph(2-F)

20-56
Me
Me
H
H
CF3
Ph(2,6-F2)

20-57
Me
Me
H
H
CF3
Ph(2-Cl)

20-58
Me
Me
H
H
CF3
Ph(2-Me)

20-59
Me
Me
H
H
CF3
Ph(2-CF3)

20-60
Me
Me
H
H
CF3
Ph(2-F-6-Cl)

20-61
Me
Me
H
H
OCF3
Ph(2-F)

20-62
Me
Me
H
H
OCF3
Ph(2,6-F2)

20-63
Me
Me
H
H
OCF3
Ph(2-Cl)

20-64
Me
Me
H
H
OCF3
Ph(2-Me)

20-65
Me
Me
H
H
OCF3
Ph(2-CF3)

20-66
Me
Me
H
H
OCF3
Ph(2-F-6-Cl)

20-67
Me
Me
H
H
OCH2CF3
Ph(2-F)

20-68
Me
Me
H
H
OCH2CF3
Ph(2,6-F2)

20-69
Me
Me
H
H
OCH2CF3
Ph(2-Cl)

20-70
Me
Me
H
H
OCH2CF3
Ph(2-Me)

20-71
Me
Me
H
H
OCH2CF3
Ph(2-CF3)

20-72
Me
Me
H
H
OCH2CF3
Ph(2-F-6-Cl)

20-73
Me
Me
H
H
OCHF2
Ph(2-F)

20-74
Me
Me
H
H
OCHF2
Ph(2,6-F2)

20-75
Me
Me
H
H
OCHF2
Ph(2-Cl)

20-76
Me
Me
H
H
OCHF2
Ph(2-Me)

20-77
Me
Me
H
H
OCHF2
Ph(2-CF3)

20-78
Me
Me
H
H
OCHF2
Ph(2-F-6-Cl)

20-79
Me
Me
H
F
Br
Ph(2-F)

20-80
Me
Me
H
F
Br
Ph(2,6-F2)

20-81
Me
Me
H
F
Br
Ph(2-Cl)

20-82
Me
Me
H
F
Br
Ph(2-Me)

20-83
Me
Me
H
F
Br
Ph(2-CF3)

20-84
Me
Me
H
F
Br
Ph(2-F-6-Cl)

20-85
Me
Me
H
F
CF3
Ph(2-F)

20-86
Me
Me
H
F
CF3
Ph(2,6-F2)

20-87
Me
Me
H
F
CF3
Ph(2-Cl)

20-88
Me
Me
H
F
CF3
Ph(2-Me)

20-89
Me
Me
H
F
CF3
Ph(2-CF3)

20-90
Me
Me
H
F
CF3
Ph(2-F-6-Cl)

20-91
Me
Me
H
F
OCF3
Ph(2-F)

20-92
Me
Me
H
F
OCF3
Ph(2,6-F2)

20-93
Me
Me
H
F
OCF3
Ph(2-Cl)

20-94
Me
Me
H
F
OCF3
Ph(2-Me)

20-95
Me
Me
H
F
OCF3
Ph(2-CF3)

20-96
Me
Me
H
F
OCF3
Ph(2-F-6-Cl)

20-97
Me
Me
H
F
OCH2CF3
Ph(2-F)

20-98
Me
Me
H
F
OCH2CF3
Ph(2,6-F2)

20-99
Me
Me
H
F
OCH2CF3
Ph(2-Cl)

20-100
Me
Me
H
F
OCH2CF3
Ph(2-Me)

20-101
Me
Me
H
F
OCH2CF3
Ph(2-CF3)

20-102
Me
Me
H
F
OCH2CF3
Ph(2-F-6-Cl)

20-103
Me
Me
H
F
OCHF2
Ph(2-F)

20-104
Me
Me
H
F
OCHF2
Ph(2,6-F2)

20-105
Me
Me
H
F
OCHF2
Ph(2-Cl)

20-106
Me
Me
H
F
OCHF2
Ph(2-Me)

20-107
Me
Me
H
F
OCHF2
Ph(2-CF3)

20-108
Me
Me
H
F
OCHF2
Ph(2-F-6-Cl)

[0260]

21

TABLE 21

Physical

Compound

properties

No.
R1
R2
R3
X1
X2
X3
X4
B
(mp ° C.)

21-1
Me
Me
H
H
H
H
H
Ph(2-F)

21-2
Me
Me
H
H
H
H
H
Ph(2,6-F2)

21-3
Me
Me
H
H
H
H
H
Ph(2-Cl)

21-4
Me
Me
H
H
H
H
H
Ph(2-Me)

21-5
Me
Me
H
H
H
H
H
Ph(2-CF3)

21-6
Me
Me
H
H
H
H
H
Ph(2-F-6-Cl)

21-7
Me
Me
H
H
H
Cl
H
Ph(2-F)

21-8
Me
Me
H
H
H
Cl
H
Ph(2,6-F2)

21-9
Me
Me
H
H
H
Cl
H
Ph(2-Cl)

21-10
Me
Me
H
H
H
Cl
H
Ph(2-Me)

21-11
Me
Me
H
H
H
Cl
H
Ph(2-CF3)

21-12
Me
Me
H
H
H
Cl
H
Ph(2-F-6-Cl)

21-13
Me
Me
H
H
H
Me
H
Ph(2-F)

21-14
Me
Me
H
H
H
Me
H
Ph(2,6-F2)

21-15
Me
Me
H
H
H
Me
H
Ph(2-Cl)

21-16
Me
Me
H
H
H
Me
H
Ph(2-Me)

21-17
Me
Me
H
H
H
Me
H
Ph(2-CF3)

21-18
Me
Me
H
H
H
Me
H
Ph(2-F-6-Cl)

21-19
Me
Me
H
H
H
H
Me
Ph(2-F)

21-20
Me
Me
H
H
H
H
Me
Ph(2,6-F2)

21-21
Me
Me
H
H
H
H
Me
Ph(2-Cl)

21-22
Me
Me
H
H
H
H
Me
Ph(2-Me)

21-23
Me
Me
H
H
H
H
Me
Ph(2-CF3)

21-24
Me
Me
H
H
H
H
Me
Ph(2-F-6-Cl)

21-25
Me
Me
H
F
F
H
H
Ph(2-F)

21-26
Me
Me
H
F
F
H
H
Ph(2,6-F2)

21-27
Me
Me
H
F
F
H
H
Ph(2-Cl)

21-28
Me
Me
H
F
F
H
H
Ph(2-Me)

21-29
Me
Me
H
F
F
H
H
Ph(2-CF3)

21-30
Me
Me
H
F
F
H
H
Ph(2-F-6-Cl)

21-31
Me
Me
H
F
F
Cl
H
Ph(2-F)

21-32
Me
Me
H
F
F
Cl
H
Ph(2,6-F2)

21-33
Me
Me
H
F
F
Cl
H
Ph(2-Cl)

21-34
Me
Me
H
F
F
Cl
H
Ph(2-Me)

21-35
Me
Me
H
F
F
Cl
H
Ph(2-CF3)

21-36
Me
Me
H
F
F
Cl
H
Ph(2-F-6-Cl)

21-37
Me
Me
H
F
F
Me
H
Ph(2-F)

21-38
Me
Me
H
F
F
Me
H
Ph(2,6-F2)

21-39
Me
Me
H
F
F
Me
H
Ph(2-Cl)

21-40
Me
Me
H
F
F
Me
H
Ph(2-Me)

21-41
Me
Me
H
F
F
Me
H
Ph(2-CF3)

21-42
Me
Me
H
F
F
Me
H
Ph(2-F-6-Cl)

21-43
Me
Me
H
F
F
H
Me
Ph(2-F)

21-44
Me
Me
H
F
F
H
Me
Ph(2,6-F2)

21-45
Me
Me
H
F
F
H
Me
Ph(2-Cl)

21-46
Me
Me
H
F
F
H
Me
Ph(2-Me)

21-47
Me
Me
H
F
F
H
Me
Ph(2-CF3)

21-48
Me
Me
H
F
F
H
Me
Ph(2-F-6-Cl)

21-49
Me
Me
H
Me
H
H
H
Ph(2-F)

21-50
Me
Me
H
Me
H
H
H
Ph(2,6-F2)

21-51
Me
Me
H
Me
H
H
H
Ph(2-Cl)

21-52
Me
Me
H
Me
H
H
H
Ph(2-Me)

21-53
Me
Me
H
Me
H
H
H
Ph(2-CF3)

21-54
Me
Me
H
Me
H
H
H
Ph(2-F-6-Cl)

21-55
Me
Me
H
Me
H
Me
H
Ph(2-F)

21-56
Me
Me
H
Me
H
Me
H
Ph(2,6-F2)

21-57
Me
Me
H
Me
H
Me
H
Ph(2-Cl)

21-58
Me
Me
H
Me
H
Me
H
Ph(2-Me)

21-59
Me
Me
H
Me
H
Me
H
Ph(2-CF3)

21-60
Me
Me
H
Me
H
Me
H
Ph(2-F-6-Cl)

21-61
Me
Me
H
Me
H
H
Me
Ph(2-F)

21-62
Me
Me
H
Me
H
H
Me
Ph(2,6-F2)

21-63
Me
Me
H
Me
H
H
Me
Ph(2-Cl)

21-64
Me
Me
H
Me
H
H
Me
Ph(2-Me)

21-65
Me
Me
H
Me
H
H
Me
Ph(2-CF3)

21-66
Me
Me
H
Me
H
H
Me
Ph(2-F-6-Cl)

21-67
Me
Me
H
F
H
H
H
Ph(2-F)

21-68
Me
Me
H
F
H
H
H
Ph(2,6-F2)

21-69
Me
Me
H
F
H
H
H
Ph(2-Cl)

21-70
Me
Me
H
F
H
H
H
Ph(2-Me)

21-71
Me
Me
H
F
H
H
H
Ph(2-CF3)

21-72
Me
Me
H
F
H
H
H
Ph(2-F-6-Cl)

21-73
Me
Me
H
H
F
H
H
Ph(2-F)

21-74
Me
Me
H
H
F
H
H
Ph(2,6-F2)

21-75
Me
Me
H
H
F
H
H
Ph(2-Cl)

21-76
Me
Me
H
H
F
H
H
Ph(2-Me)

21-77
Me
Me
H
H
F
H
H
Ph(2-CF3)

21-78
Me
Me
H
H
F
H
H
Ph(2-F-6-Cl)

21-79
Me
Me
H
F
H
Me
H
Ph(2-F)

21-80
Me
Me
H
F
H
Me
H
Ph(2,6-F2)

21-81
Me
Me
H
F
H
Me
H
Ph(2-Cl)

21-82
Me
Me
H
F
H
Me
H
Ph(2-Me)

21-83
Me
Me
H
F
H
Me
H
Ph(2-CF3)

21-84
Me
Me
H
F
H
Me
H
Ph(2-F-6-Cl)

21-85
Me
Me
H
H
F
Me
H
Ph(2-F)

21-86
Me
Me
H
H
F
Me
H
Ph(2,6-F2)

21-87
Me
Me
H
H
F
Me
H
Ph(2-Cl)

21-88
Me
Me
H
H
F
Me
H
Ph(2-Me)

21-89
Me
Me
H
H
F
Me
H
Ph(2-CF3)

21-90
Me
Me
H
H
F
Me
H
Ph(2-F-6-Cl)

21-91
Me
Me
H
F
H
H
Me
Ph(2-F)

21-92
Me
Me
H
F
H
H
Me
Ph(2,6-F2)

21-93
Me
Me
H
F
H
H
Me
Ph(2-Cl)

21-94
Me
Me
H
F
H
H
Me
Ph(2-Me)

21-95
Me
Me
H
F
H
H
Me
Ph(2-CF3)

21-96
Me
Me
H
F
H
H
Me
Ph(2-F-6-Cl)

21-97
Me
Me
H
H
F
H
Me
Ph(2-F)

21-98
Me
Me
H
H
F
H
Me
Ph(2,6-F2)

21-99
Me
Me
H
H
F
H
Me
Ph(2-Cl)

21-100
Me
Me
H
H
F
H
Me
Ph(2-Me)

21-101
Me
Me
H
H
F
H
Me
Ph(2-CF3)

21-102
Me
Me
H
H
F
H
Me
Ph(2-F-6-Cl)

21-103
Me
Me
H
F
H
Cl
H
Ph(2-F)

21-104
Me
Me
H
F
H
Cl
H
Ph(2,6-F2)

21-105
Me
Me
H
F
H
Cl
H
Ph(2-Cl)

21-106
Me
Me
H
F
H
Cl
H
Ph(2-Me)

21-107
Me
Me
H
F
H
Cl
H
Ph(2-CF3)

21-108
Me
Me
H
F
H
Cl
H
Ph(2-F-6-Cl)

21-109
Me
Me
H
H
F
Cl
H
Ph(2-F)

21-110
Me
Me
H
H
F
Cl
H
Ph(2,6-F2)

21-111
Me
Me
H
H
F
Cl
H
Ph(2-Cl)

21-112
Me
Me
H
H
F
Cl
H
Ph(2-Me)

21-113
Me
Me
H
H
F
Cl
H
Ph(2-CF3)

21-114
Me
Me
H
H
F
Cl
H
Ph(2-F-6-Cl)

21-115
Me
Me
H
F
H
H
Cl
Ph(2-F)

21-116
Me
Me
H
F
H
H
Cl
Ph(2,6-F2)

21-117
Me
Me
H
F
H
H
Cl
Ph(2-Cl)

21-118
Me
Me
H
F
H
H
Cl
Ph(2-Me)

21-119
Me
Me
H
F
H
H
Cl
Ph(2-CF3)

21-120
Me
Me
H
F
H
H
Cl
Ph(2-F-6-Cl)

21-121
Me
Me
H
H
F
H
Cl
Ph(2-F)

21-122
Me
Me
H
H
F
H
Cl
Ph(2,6-F2)

21-123
Me
Me
H
H
F
H
Cl
Ph(2-Cl)

21-124
Me
Me
H
H
F
H
Cl
Ph(2-Me)

21-125
Me
Me
H
H
F
H
Cl
Ph(2-CF3)

21-126
Me
Me
H
H
F
H
Cl
Ph(2-F-6-Cl)

21-127
Me
Me
H
Me
H
Cl
H
Ph(2-F)

21-128
Me
Me
H
Me
H
Cl
H
Ph(2,6-F2)

21-129
Me
Me
H
Me
H
Cl
H
Ph(2-Cl)

21-130
Me
Me
H
Me
H
Cl
H
Ph(2-Me)

21-131
Me
Me
H
Me
H
Cl
H
Ph(2-CF3)

21-132
Me
Me
H
Me
H
Cl
H
Ph(2-F-6-Cl)

21-133
Me
Me
H
Me
H
H
Cl
Ph(2-F)

21-134
Me
Me
H
Me
H
H
Cl
Ph(2,6-F2)

21-135
Me
Me
H
Me
H
H
Cl
Ph(2-Cl)

21-136
Me
Me
H
Me
H
H
Cl
Ph(2-Me)

21-137
Me
Me
H
Me
H
H
Cl
Ph(2-CF3)

21-138
Me
Me
H
Me
H
H
Cl
Ph(2-F-6-Cl)

[0261]

22

TABLE 22

Phys1cal

Compound

propert1es

No.
R1
R2
R3
X1
X2
X3
X4
B
(mp ° C.)

22-1
Me
Me
H
Me
H
H
H
Ph(2-F)

22-2
Me
Me
H
Me
H
H
H
Ph(2,6-F2)

22-3
Me
Me
H
Me
H
H
H
Ph(2-Cl)

22-4
Me
Me
H
Me
H
H
H
Ph(2-Me)

22-5
Me
Me
H
Me
H
H
H
Ph(2-CF3)

22-6
Me
Me
H
Me
H
H
H
Ph(2-F-6-Cl)

22-7
Me
Me
H
Me
H
Cl
H
Ph(2-F)

22-8
Me
Me
H
Me
H
Cl
H
Ph(2,6-F2)

22-9
Me
Me
H
Me
H
Cl
H
Ph(2-Cl)

22-10
Me
Me
H
Me
H
Cl
H
Ph(2-Me)

22-11
Me
Me
H
Me
H
Cl
H
Ph(2-CF3)

22-12
Me
Me
H
Me
H
Cl
H
Ph(2-F-6-Cl)

22-13
Me
Me
H
Me
H
Me
H
Ph(2-F)

22-14
Me
Me
H
Me
H
Me
H
Ph(2,6-F2)

22-15
Me
Me
H
Me
H
Me
H
Ph(2-Cl)

22-16
Me
Me
H
Me
H
Me
H
Ph(2-Me)

22-17
Me
Me
H
Me
H
Me
H
Ph(2-CF3)

22-18
Me
Me
H
Me
H
Me
H
Ph(2-F-6-Cl)

22-19
Me
Me
H
Me
H
H
Me
Ph(2-F)

22-20
Me
Me
H
Me
H
H
Me
Ph(2,6-F2)

22-21
Me
Me
H
Me
H
H
Me
Ph(2-Cl)

22-22
Me
Me
H
Me
H
H
Me
Ph(2-Me)

22-23
Me
Me
H
Me
H
H
Me
Ph(2-CF3)

22-24
Me
Me
H
Me
H
H
Me
Ph(2-F-6-Cl)

22-25
Me
Me
H
H
Me
H
H
Ph(2-F)

22-26
Me
Me
H
H
Me
H
H
Ph(2,6-F2)

22-27
Me
Me
H
H
Me
H
H
Ph(2-Cl)

22-28
Me
Me
H
H
Me
H
H
Ph(2-Me)

22-29
Me
Me
H
H
Me
H
H
Ph(2-CF3)

22-30
Me
Me
H
H
Me
H
H
Ph(2-F-6-Cl)

22-31
Me
Me
H
H
Me
Cl
H
Ph(2-F)

22-32
Me
Me
H
H
Me
Cl
H
Ph(2,6-F2)

22-33
Me
Me
H
H
Me
Cl
H
Ph(2-Cl)

22-34
Me
Me
H
H
Me
Cl
H
Ph(2-Me)

22-35
Me
Me
H
H
Me
Cl
H
Ph(2-CF3)

22-36
Me
Me
H
H
Me
Cl
H
Ph(2-F-6-Cl)

22-37
Me
Me
H
H
Me
Me
H
Ph(2-F)

22-38
Me
Me
H
H
Me
Me
H
Ph(2,6-F2)

22-39
Me
Me
H
H
Me
Me
H
Ph(2-Cl)

22-40
Me
Me
H
H
Me
Me
H
Ph(2-Me)

22-41
Me
Me
H
H
Me
Me
H
Ph(2-CF3)

22-42
Me
Me
H
H
Me
Me
H
Ph(2-F-6-Cl)

22-43
Me
Me
H
H
Me
H
Me
Ph(2-F)

22-44
Me
Me
H
H
Me
H
Me
Ph(2,6-F2)

22-45
Me
Me
H
H
Me
H
Me
Ph(2-Cl)

22-46
Me
Me
H
H
Me
H
Me
Ph(2-Me)

22-47
Me
Me
H
H
Me
H
Me
Ph(2-CF3)

22-48
Me
Me
H
H
Me
H
Me
Ph(2-F-6-Cl)

[0262]

23

TABLE 23

Physical

Compound

properties

No.
R1
R2
R3
X1
X2
X3
X4
B
(mp ° C.)

23-1
Me
Me
H
H
H
H
H
Ph(2-F)

23-1
Me
Me
H
H
H
H
H
Ph(2-F)

23-2
Me
Me
H
H
H
H
H
Ph(2,6-F2)

23-3
Me
Me
H
H
H
H
H
Ph(2-Cl)

23-4
Me
Me
H
H
H
H
H
Ph(2-Me)

23-5
Me
Me
H
H
H
H
H
Ph(2-CF3)

23-6
Me
Me
H
H
H
H
H
Ph(2-F-6-Cl)

23-7
Me
Me
H
H
H
Cl
H
Ph(2-F)

23-8
Me
Me
H
H
H
Cl
H
Ph(2,6-F2)

23-9
Me
Me
H
H
H
Cl
H
Ph(2-Cl)

23-10
Me
Me
H
H
H
Cl
H
Ph(2-Me)

23-11
Me
Me
H
H
H
Cl
H
Ph(2-CF3)

23-12
Me
Me
H
H
H
Cl
H
Ph(2-F-6-Cl)

23-13
Me
Me
H
H
H
Me
H
Ph(2-F)

23-14
Me
Me
H
H
H
Me
H
Ph(2,6-F2)

23-15
Me
Me
H
H
H
Me
H
Ph(2-Cl)

23-16
Me
Me
H
H
H
Me
H
Ph(2-Me)

23-17
Me
Me
H
H
H
Me
H
Ph(2-CF3)

23-18
Me
Me
H
H
H
Me
H
Ph(2-F-6-Cl)

23-19
Me
Me
H
H
H
H
Me
Ph(2-F)

23-20
Me
Me
H
H
H
H
Me
Ph(2,6-F2)

23-21
Me
Me
H
H
H
H
Me
Ph(2-Cl)

23-22
Me
Me
H
H
H
H
Me
Ph(2-Me)

23-23
Me
Me
H
H
H
H
Me
Ph(2-CF3)

23-24
Me
Me
H
H
H
H
Me
Ph(2-F-6-Cl)

23-25
Me
Me
H
F
F
H
H
Ph(2-F)

23-26
Me
Me
H
F
F
H
H
Ph(2,6-F2)

23-27
Me
Me
H
F
F
H
H
Ph(2-Cl)

23-28
Me
Me
H
F
F
H
H
Ph(2-Me)

23-29
Me
Me
H
F
F
H
H
Ph(2-CF3)

23-30
Me
Me
H
F
F
H
H
Ph(2-F-6-Cl)

23-31
Me
Me
H
F
F
Cl
H
Ph(2-F)

23-32
Me
Me
H
F
F
Cl
H
Ph(2,6-F2)

23-33
Me
Me
H
F
F
Cl
H
Ph(2-Cl)

23-34
Me
Me
H
F
F
Cl
H
Ph(2-Me)

23-35
Me
Me
H
F
F
Cl
H
Ph(2-CF3)

23-36
Me
Me
H
F
F
Cl
H
Ph(2-F-6-Cl)

23-37
Me
Me
H
F
F
Me
H
Ph(2-F)

23-38
Me
Me
H
F
F
Me
H
Ph(2,6-F2)

23-39
Me
Me
H
F
F
Me
H
Ph(2-Cl)

23-40
Me
Me
H
F
F
Me
H
Ph(2-Me)

23-41
Me
Me
H
F
F
Me
H
Ph(2-CF3)

23-42
Me
Me
H
F
F
Me
H
Ph(2-F-6-Cl)

23-43
Me
Me
H
F
F
H
Me
Ph(2-F)

23-44
Me
Me
H
F
F
H
Me
Ph(2,6-F2)

23-45
Me
Me
H
F
F
H
Me
Ph(2-Cl)

23-46
Me
Me
H
F
F
H
Me
Ph(2-Me)

23-47
Me
Me
H
F
F
H
Me
Ph(2-CF3)

23-48
Me
Me
H
F
F
H
Me
Ph(2-F-6-Cl)

23-49
Me
Me
H
H
H
H
Cl
Ph(2-F)

23-50
Me
Me
H
H
H
H
Cl
Ph(2,6-F2)

23-51
Me
Me
H
H
H
H
Cl
Ph(2-Cl)

23-52
Me
Me
H
H
H
H
Cl
Ph(2-Me)

23-53
Me
Me
H
H
H
H
Cl
Ph(2-CF3)

23-54
Me
Me
H
H
H
H
Cl
Ph(2-F-6-Cl)

23-55
Me
Me
H
F
F
H
Cl
Ph(2-F)

23-56
Me
Me
H
F
F
H
Cl
Ph(2,6-F2)

23-57
Me
Me
H
F
F
H
Cl
Ph(2-Cl)

23-58
Me
Me
H
F
F
H
Cl
Ph(2-Me)

23-59
Me
Me
H
F
F
H
Cl
Ph(2-CF3)

23-60
Me
Me
H
F
F
H
Cl
Ph(2-F-6-Cl)

23-61
Me
Me
H
F
H
Cl
H
Ph(2-F)

23-62
Me
Me
H
F
H
Cl
H
Ph(2,6-F2)

23-63
Me
Me
H
F
H
Cl
H
Ph(2-Cl)

23-64
Me
Me
H
F
H
Cl
H
Ph(2-Me)

23-65
Me
Me
H
F
H
Cl
H
Ph(2-CF3)

23-66
Me
Me
H
F
H
Cl
H
Ph(2-F-6-Cl)

23-67
Me
Me
H
H
F
Cl
H
Ph(2-F)

23-68
Me
Me
H
H
F
Cl
H
Ph(2,6-F2)

23-69
Me
Me
H
H
F
Cl
H
Ph(2-Cl)

23-70
Me
Me
H
H
F
Cl
H
Ph(2-Me)

23-71
Me
Me
H
H
F
Cl
H
Ph(2-CF3)

23-72
Me
Me
H
H
F
Cl
H
Ph(2-F-6-Cl)

23-73
Me
Me
H
F
H
Me
H
Ph(2-F)

23-74
Me
Me
H
F
H
Me
H
Ph(2,6-F2)

23-75
Me
Me
H
F
H
Me
H
Ph(2-Cl)

23-76
Me
Me
H
F
H
Me
H
Ph(2-Me)

23-77
Me
Me
H
F
H
Me
H
Ph(2-CF3)

23-78
Me
Me
H
F
H
Me
H
Ph(2-F-6-Cl)

23-79
Me
Me
H
H
F
Me
H
Ph(2-F)

23-80
Me
Me
H
H
F
Me
H
Ph(2,6-F2)

23-81
Me
Me
H
H
F
Me
H
Ph(2-Cl)

23-82
Me
Me
H
H
F
Me
H
Ph(2-Me)

23-83
Me
Me
H
H
F
Me
H
Ph(2-CF3)

23-84
Me
Me
H
H
F
Me
H
Ph(2-F-6-Cl)

23-85
Me
Me
H
F
H
H
Cl
Ph(2-F)

23-86
Me
Me
H
F
H
H
Cl
Ph(2,6-F2)

23-87
Me
Me
H
F
H
H
Cl
Ph(2-Cl)

23-88
Me
Me
H
F
H
H
Cl
Ph(2-Me)

23-89
Me
Me
H
F
H
H
Cl
Ph(2-CF3)

23-90
Me
Me
H
F
H
H
Cl
Ph(2-F-6-Cl)

23-91
Me
Me
H
H
F
H
Me
Ph(2-F)

23-92
Me
Me
H
H
F
H
Me
Ph(2,6-F2)

23-93
Me
Me
H
H
F
H
Me
Ph(2-Cl)

23-94
Me
Me
H
H
F
H
Me
Ph(2-Me)

23-95
Me
Me
H
H
F
H
Me
Ph(2-CF3)

23-96
Me
Me
H
H
F
H
Me
Ph(2-F-6-Cl)

23-97
Me
Me
H
F
H
H
Me
Ph(2-F)

23-98
Me
Me
H
F
H
H
Me
Ph(2,6-F2)

23-99
Me
Me
H
F
H
H
Me
Ph(2-Cl)

23-100
Me
Me
H
F
H
H
Me
Ph(2-Me)

23-101
Me
Me
H
F
H
H
Me
Ph(2-CF3)

23-102
Me
Me
H
F
H
H
Me
Ph(2-F-6-Cl)

23-103
Me
Me
H
H
F
H
Me
Ph(2-F)

23-104
Me
Me
H
H
F
H
Me
Ph(2,6-F2)

23-105
Me
Me
H
H
F
H
Me
Ph(2-Cl)

23-106
Me
Me
H
H
F
H
Me
Ph(2-Me)

23-107
Me
Me
H
H
F
H
Me
Ph(2-CF3)

23-108
Me
Me
H
H
F
H
Me
Ph(2-F-6-Cl)

[0263]

24

TABLE 24

Com-

Physical

pound

properties

No.
R1
R2
R3
X1
X2
X3
X4
B
(mp ° C.)

24-1
Me
Me
H
H
H
H
H
Ph(2-F)

24-2
Me
Me
H
H
H
H
H
Ph(2,6-F2)

24-3
Me
Me
H
H
H
H
H
Ph(2-Cl)

24-4
Me
Me
H
H
H
H
H
Ph(2-Me)

24-5
Me
Me
H
H
H
H
H
Ph(2-CF3)

24-6
Me
Me
H
H
H
H
H
Ph(2-F-6-Cl)

24-7
Me
Me
H
H
H
H
Me
Ph(2-F)

24-8
Me
Me
H
H
H
H
Me
Ph(2,6-F2)

24-9
Me
Me
H
H
H
H
Me
Ph(2-Cl)

24-10
Me
Me
H
H
H
H
Me
Ph(2-Me)

24-11
Me
Me
H
H
H
H
Me
Ph(2-CF3)

24-12
Me
Me
H
H
H
H
Me
Ph(2-F-6-Cl)

24-13
Me
Me
H
F
H
H
H
Ph(2-F)

24-14
Me
Me
H
F
H
H
H
Ph(2,6-F2)

24-15
Me
Me
H
F
H
H
H
Ph(2-Cl)

24-16
Me
Me
H
F
H
H
H
Ph(2-Me)

24-17
Me
Me
H
F
H
H
H
Ph(2-CF3)

24-18
Me
Me
H
F
H
H
H
Ph(2-F-6-Cl)

24-19
Me
Me
H
F
H
H
Me
Ph(2-F)

24-20
Me
Me
H
F
H
H
Me
Ph(2,6-F2)

24-21
Me
Me
H
F
H
H
Me
Ph(2-Cl)

24-22
Me
Me
H
F
H
H
Me
Ph(2-Me)

24-23
Me
Me
H
F
H
H
Me
Ph(2-CF3)

24-24
Me
Me
H
F
H
H
Me
Ph(2-F-6-Cl)

24-25
Me
Me
H
H
F
H
H
Ph(2-F)

24-26
Me
Me
H
H
F
H
H
Ph(2,6-F2)

24-27
Me
Me
H
H
F
H
H
Ph(2-Cl)

24-28
Me
Me
H
H
F
H
H
Ph(2-Me)

24-29
Me
Me
H
H
F
H
H
Ph(2-CF3)

24-30
Me
Me
H
H
F
H
H
Ph(2-F-6-Cl)

24-31
Me
Me
H
H
F
H
Me
Ph(2-F)

24-32
Me
Me
H
H
F
H
Me
Ph(2,6-F2)

24-33
Me
Me
H
H
F
H
Me
Ph(2-Cl)

24-34
Me
Me
H
H
F
H
Me
Ph(2-Me)

24-35
Me
Me
H
H
F
H
Me
Ph(2-CF3)

24-36
Me
Me
H
H
F
H
Me
Ph(2-F-6-Cl)

24-37
Me
Me
H
F
F
H
H
Ph(2-F)

24-38
Me
Me
H
F
F
H
H
Ph(2,6-F2)

24-39
Me
Me
H
F
F
H
H
Ph(2-Cl)

24-40
Me
Me
H
F
F
H
H
Ph(2-Me)

24-41
Me
Me
H
F
F
H
H
Ph(2-CF3)

24-42
Me
Me
H
F
F
H
H
Ph(2-F-6-Cl)

24-43
Me
Me
H
F
F
H
Me
Ph(2-F)

24-44
Me
Me
H
F
F
H
Me
Ph(2,6-F2)

24-45
Me
Me
H
F
F
H
Me
Ph(2-Cl)

24-46
Me
Me
H
F
F
H
Me
Ph(2-Me)

24-47
Me
Me
H
F
F
H
Me
Ph(2-CF3)

24-48
Me
Me
H
F
F
H
Me
Ph(2-F-6-Cl)

24-49
Me
Me
H
H
H
Me
Me
Ph(2-F)

24-50
Me
Me
H
H
H
Me
Me
Ph(2,6-F2)

24-51
Me
Me
H
H
H
Me
Me
Ph(2-Cl)

24-52
Me
Me
H
H
H
Me
Me
Ph(2-Me)

24-53
Me
Me
H
H
H
Me
Me
Ph(2-CF3)

24-54
Me
Me
H
H
H
Me
Me
Ph(2-F-6-Cl)

24-55
Me
Me
H
H
H
OMe
Me
Ph(2-F)

24-56
Me
Me
H
H
H
OMe
Me
Ph(2,6-F2)

24-57
Me
Me
H
H
H
OMe
Me
Ph(2-Cl)

24-58
Me
Me
H
H
H
OMe
Me
Ph(2-Me)

24-59
Me
Me
H
H
H
OMe
Me
Ph(2-CF3)

24-60
Me
Me
H
H
H
OMe
Me
Ph(2-F-6-Cl)

24-61
Me
Me
H
H
H
OH
Me
Ph(2-F)

24-62
Me
Me
H
H
H
OH
Me
Ph(2,6-F2)

24-63
Me
Me
H
H
H
OH
Me
Ph(2-Cl)

24-64
Me
Me
H
H
H
OH
Me
Ph(2-Me)

24-65
Me
Me
H
H
H
OH
Me
Ph(2-CF3)

24-66
Me
Me
H
H
H
OH
Me
Ph(2-F-6-Cl)

24-67
Me
Me
H
Me
H
H
Me
Ph(2-F)

24-68
Me
Me
H
Me
H
H
Me
Ph(2,6-F2)

24-69
Me
Me
H
Me
H
H
Me
Ph(2-Cl)

24-70
Me
Me
H
Me
H
H
Me
Ph(2-Me)

24-71
Me
Me
H
Me
H
H
Me
Ph(2-CF3)

24-72
Me
Me
H
Me
H
H
Me
Ph(2-F-6-Cl)

24-73
Me
Me
H
H
H
H
Cl
Ph(2-F)

24-74
Me
Me
H
H
H
H
Cl
Ph(2,6-F2)

24-75
Me
Me
H
H
H
H
Cl
Ph(2-Cl)

24-76
Me
Me
H
H
H
H
Cl
Ph(2-Me)

24-77
Me
Me
H
H
H
H
Cl
Ph(2-CF3)

24-78
Me
Me
H
H
H
H
Cl
Ph(2-F-6-Cl)

24-79
Me
Me
H
F
H
H
Cl
Ph(2-F)

24-80
Me
Me
H
F
H
H
Cl
Ph(2,6-F2)

24-81
Me
Me
H
F
H
H
Cl
Ph(2-Cl)

24-82
Me
Me
H
F
H
H
Cl
Ph(2-Me)

24-83
Me
Me
H
F
H
H
Cl
Ph(2-CF3)

24-84
Me
Me
H
F
H
H
Cl
Ph(2-F-6-Cl)

24-85
Me
Me
H
H
F
H
Cl
Ph(2-F)

24-86
Me
Me
H
H
F
H
Cl
Ph(2,6-F2)

24-87
Me
Me
H
H
F
H
Cl
Ph(2-Cl)

24-88
Me
Me
H
H
F
H
Cl
Ph(2-Me)

24-89
Me
Me
H
H
F
H
Cl
Ph(2-CF3)

24-90
Me
Me
H
H
F
H
Cl
Ph(2-F-6-Cl)

24-91
Me
Me
H
F
F
H
Cl
Ph(2-F)

24-92
Me
Me
H
F
F
H
Cl
Ph(2,6-F2)

24-93
Me
Me
H
F
F
H
Cl
Ph(2-Cl)

24-94
Me
Me
H
F
F
H
Cl
Ph(2-Me)

24-95
Me
Me
H
F
F
H
Cl
Ph(2-CF3)

24-96
Me
Me
H
F
F
H
Cl
Ph(2-F-6-Cl)

24-97
Me
Me
H
H
H
Me
Cl
Ph(2-F)

24-98
Me
Me
H
H
H
Me
Cl
Ph(2,6-F2)

24-99
Me
Me
H
H
H
Me
Cl
Ph(2-Cl)

24-100
Me
Me
H
H
H
Me
Cl
Ph(2-Me)

24-101
Me
Me
H
H
H
Me
Cl
Ph(2-CF3)

24-102
Me
Me
H
H
H
Me
Cl
Ph(2-F-6-Cl)

24-103
Me
Me
H
H
H
OMe
Cl
Ph(2-F)

24-104
Me
Me
H
H
H
OMe
Cl
Ph(2,6-F2)

24-105
Me
Me
H
H
H
OMe
Cl
Ph(2-Cl)

24-106
Me
Me
H
H
H
OMe
Cl
Ph(2-Me)

24-107
Me
Me
H
H
H
OMe
Cl
Ph(2-CF3)

24-108
Me
Me
H
H
H
ONe
Cl
Ph(2-F-6-Cl)

24-109
Me
Me
H
H
H
OH
Cl
Ph(2-F)

24-110
Me
Me
H
H
H
OH
Cl
Ph(2,6-F2)

24-111
Me
Me
H
H
H
OH
Cl
Ph(2-Cl)

24-112
Me
Me
H
H
H
OH
Cl
Ph(2-Me)

24-113
Me
Me
H
H
H
OH
Cl
Ph(2-CF3)

24-114
Me
Me
H
H
H
OH
Cl
Ph(2-F-6-Cl)

24-115
Me
Me
H
Me
H
H
Cl
Ph(2-F)

24-116
Me
Me
H
Me
H
H
Cl
Ph(2,6-F2)

24-117
Me
Me
H
Me
H
H
Cl
Ph(2-Cl)

24-118
Me
Me
H
Me
H
H
Cl
Ph(2-Me)

24-119
Me
Me
H
Me
H
H
Cl
Ph(2-CF3)

24-120
Me
Me
H
Me
H
H
Cl
Ph(2-F-6-Cl)

[0264]

25

TABLE 25

Physical

Compound

properties

No.
R1
R2
R3
X1
X2
B
(mp ° C.)

25-1
Me
Me
H
H
H
Ph(2-F)

25-2
Me
Me
H
H
H
Ph(2,6-F2)

25-3
Me
Me
H
H
H
Ph(2-Cl)

25-4
Me
Me
H
H
H
Ph(2-Me)

25-5
Me
Me
H
H
H
Ph(2-CF3)

25-6
Me
Me
H
H
H
Ph(2-F-6-Cl)

25-7
Me
Me
H
Cl
H
Ph(2-F)

25-8
Me
Me
H
Cl
H
Ph(2,6-F2)

25-9
Me
Me
H
Cl
H
Ph(2-Cl)

25-10
Me
Me
H
Cl
H
Ph(2-Me)

25-11
Me
Me
H
Cl
H
Ph(2-CF3)

25-12
Me
Me
H
Cl
H
Ph(2-F-6-Cl)

25-13
Me
Me
H
Me
H
Ph(2-F)

25-14
Me
Me
H
Me
H
Ph(2,6-F2)

25-15
Me
Me
H
Me
H
Ph(2-Cl)

25-16
Me
Me
H
Me
H
Ph(2-Me)

25-17
Me
Me
H
Me
H
Ph(2-CF3)

25-18
Me
Me
H
Me
H
Ph(2-F-6-Cl)

25-19
Me
Me
H
H
Cl
Ph(2-F)

25-20
Me
Me
H
H
Cl
Ph(2,6-F2)

25-21
Me
Me
H
H
Cl
Ph(2-Cl)

25-22
Me
Me
H
H
Cl
Ph(2-Me)

25-23
Me
Me
H
H
Cl
Ph(2-CF3)

25-24
Me
Me
H
H
Cl
Ph(2-F-6-Cl)

25-25
Me
Me
H
H
Me
Ph(2-F)

25-26
Me
Me
H
H
Me
Ph(2,6-F2)

25-27
Me
Me
H
H
Me
Ph(2-Cl)

25-28
Me
Me
H
H
Me
Ph(2-Me)

25-29
Me
Me
H
H
Me
Ph(2-CF3)

25-30
Me
Me
H
H
Me
Ph(2-F-6-Cl)

25-31
Me
Me
H
Me
Me
Ph(2-F)

25-32
Me
Me
H
Me
Me
Ph(2,6-F2)

25-33
Me
Me
H
Me
Me
Ph(2-Cl)

25-34
Me
Me
H
Me
Me
Ph(2-Me)

25-35
Me
Me
H
Me
Me
Ph(2-CF3)

25-36
Me
Me
H
Me
Me
Ph(2-F-6-Cl)

[0265]

26

TABLE 26

Physical

Compound

properties

No.
R1
R2
R3
X1
X2
B
(mp ° C.)

26-1
Me
Me
H
H
H
Ph(2-F)

26-2
Me
Me
H
H
H
Ph(2,6-F2)

26-3
Me
Me
H
H
H
Ph(2-Cl)

26-4
Me
Me
H
H
H
Ph(2-Me)

26-5
Me
Me
H
H
H
Ph(2-CF3)

26-6
Me
Me
H
H
H
Ph(2-F-6-Cl)

26-7
Me
Me
H
Cl
H
Ph(2-F)

26-8
Me
Me
H
Cl
H
Ph(2,6-F2)

26-9
Me
Me
H
Cl
H
Ph(2-Cl)

26-10
Me
Me
H
Cl
H
Ph(2-Me)

26-11
Me
Me
H
Cl
H
Ph(2-CF3)

26-12
Me
Me
H
Cl
H
Ph(2-F-6-Cl)

26-13
Me
Me
H
Me
H
Ph(2-F)

26-14
Me
Me
H
Me
H
Ph(2,6-F2)

26-15
Me
Me
H
Me
H
Ph(2-Cl)

26-16
Me
Me
H
Me
H
Ph(2-Me)

26-17
Me
Me
H
Me
H
Ph(2-CF3)

26-18
Me
Me
H
Me
H
Ph(2-F-6-Cl)

26-19
Me
Me
H
H
Cl
Ph(2-F)

26-20
Me
Me
H
H
Cl
Ph(2,6-F2)

26-21
Me
Me
H
H
Cl
Ph(2-Cl)

26-22
Me
Me
H
H
Cl
Ph(2-Me)

26-23
Me
Me
H
H
Cl
Ph(2-CF3)

26-24
Me
Me
H
H
Cl
Ph(2-F-6-Cl)

26-25
Me
Me
H
H
Me
Ph(2-F)

26-26
Me
Me
H
H
Me
Ph(2,6-F2)

26-27
Me
Me
H
H
Me
Ph(2-Cl)

26-28
Me
Me
H
H
Me
Ph(2-Me)

26-29
Me
Me
H
H
Me
Ph(2-CF3)

26-30
Me
Me
H
H
Me
Ph(2-F-6-Cl)

26-31
Me
Me
H
Me
Me
Ph(2-F)

26-32
Me
Me
H
Me
Me
Ph(2,6-F2)

26-33
Me
Me
H
Me
Me
Ph(2-Cl)

26-34
Me
Me
H
Me
Me
Ph(2-Me)

26-35
Me
Me
H
Me
Me
Ph(2-CF3)

26-36
Me
Me
H
Me
Me
Ph(2-F-6-Cl)

[0266]

27

TABLE 27

Physical

Compound

properties

No.
R1
R2
R3
X1
X2
B
(mp ° C.)

27-1
Me
Me
H
H
H
Ph(2-F)

27-2
Me
Me
H
H
H
Ph(2,6-F2)

27-3
Me
Me
H
H
H
Ph(2-Cl)

27-4
Me
Me
H
H
H
Ph(2-Me)

27-5
Me
Me
H
H
H
Ph(2-CF3)

27-6
Me
Me
H
H
H
Ph(2-F-6-Cl)

27-7
Me
Me
H
Cl
H
Ph(2-F)

27-8
Me
Me
H
Cl
H
Ph(2,6-F2)

27-9
Me
Me
H
Cl
H
Ph(2-Cl)

27-10
Me
Me
H
Cl
H
Ph(2-Me)

27-11
Me
Me
H
Cl
H
Ph(2-CF3)

27-12
Me
Me
H
Cl
H
Ph(2-F-6-Cl)

27-13
Me
Me
H
Me
H
Ph(2-F)

27-14
Me
Me
H
Me
H
Ph(2,6-F2)

27-15
Me
Me
H
Me
H
Ph(2-Cl)

27-16
Me
Me
H
Me
H
Ph(2-Me)

27-17
Me
Me
H
Me
H
Ph(2-CF3)

27-18
Me
Me
H
Me
H
Ph(2-F-6-Cl)

27-19
Me
Me
H
H
Cl
Ph(2-F)

27-20
Me
Me
H
H
Cl
Ph(2,6-F2)

27-21
Me
Me
H
H
Cl
Ph(2-Cl)

27-22
Me
Me
H
H
Cl
Ph(2-Me)

27-23
Me
Me
H
H
Cl
Ph(2-CF3)

27-24
Me
Me
H
H
Cl
Ph(2-F-6-Cl)

27-25
Me
Me
H
H
Me
Ph(2-F)

27-26
Me
Me
H
H
Me
Ph(2,6-F2)

27-27
Me
Me
H
H
Me
Ph(2-Cl)

27-28
Me
Me
H
H
Me
Ph(2-Me)

27-29
Me
Me
H
H
Me
Ph(2-CF3)

27-30
Me
Me
H
H
Me
Ph(2-F-6-Cl)

27-31
Me
Me
H
Me
Me
Ph(2-F)

27-32
Me
Me
H
Me
Me
Ph(2,6-F2)

27-33
Me
Me
H
Me
Me
Ph(2-Cl)

27-34
Me
Me
H
Me
Me
Ph(2-Me)

27-35
Me
Me
H
Me
Me
Ph(2-CF3)

27-36
Me
Me
H
Me
Me
Ph(2-F-6-Cl)

[0267]

28

TABLE 28

Physical

Compound

properties

No.
R1
R2
R3
X1
X2
B
(mp ° C.)

28-1
Me
Me
H
H
H
Ph(2-F)

28-2
Me
Me
H
H
H
Ph(2,6-F2)

28-3
Me
Me
H
H
H
Ph(2-Cl)

28-4
Me
Me
H
H
H
Ph(2-Me)

28-5
Me
Me
H
H
H
Ph(2-CF3)

28-6
Me
Me
H
H
H
Ph(2-F-6-Cl)

28-7
Me
Me
H
Cl
H
Ph(2-F)

28-8
Me
Me
H
Cl
H
Ph(2,6-F2)

28-9
Me
Me
H
Cl
H
Ph(2-Cl)

28-10
Me
Me
H
Cl
H
Ph(2-Me)

28-11
Me
Me
H
Cl
H
Ph(2-CF3)

28-12
Me
Me
H
Cl
H
Ph(2-F-6-Cl)

28-13
Me
Me
H
Me
H
Ph(2-F)

28-14
Me
Me
H
Me
H
Ph(2,6-F2)

28-15
Me
Me
H
Me
H
Ph(2-Cl)

28-16
Me
Me
H
Me
H
Ph(2-Me)

28-17
Me
Me
H
Me
H
Ph(2-CF3)

28-18
Me
Me
H
Me
H
Ph(2-F-6-Cl)

28-19
Me
Me
H
H
Cl
Ph(2-F)

28-20
Me
Me
H
H
Cl
Ph(2,6-F2)

28-21
Me
Me
H
H
Cl
Ph(2-Cl)

28-22
Me
Me
H
H
Cl
Ph(2-Me)

28-23
Me
Me
H
H
Cl
Ph(2-CF3)

28-24
Me
Me
H
H
Cl
Ph(2-F-6-Cl)

28-25
Me
Me
H
H
Me
Ph(2-F)

28-26
Me
Me
H
H
Me
Ph(2,6-F2)

28-27
Me
Me
H
H
Me
Ph(2-Cl)

28-28
Me
Me
H
H
Me
Ph(2-Me)

28-29
Me
Me
H
H
Me
Ph(2-CF3)

28-30
Me
Me
H
H
Me
Ph(2-F-6-Cl)

28-31
Me
Me
H
Me
Me
Ph(2-F)

28-32
Me
Me
H
Me
Me
Ph(2,6-F2)

28-33
Me
Me
H
Me
Me
Ph(2-Cl)

28-34
Me
Me
H
Me
Me
Ph(2-Me)

28-35
Me
Me
H
Me
Me
Ph(2-CF3)

28-36
Me
Me
H
Me
Me
Ph(2-F-6-Cl)

[0268]

29

TABLE 29

Physical

Compound

properties

No.
R1
R2
R3
X1
X2
B
(mp ° C.)

29-1
Me
Me
H
H
H
Ph(2-F)

29-2
Me
Me
H
H
H
Ph(2,6-F2)

29-3
Me
Me
H
H
H
Ph(2-Cl)

29-4
Me
Me
H
H
H
Ph(2-Me)

29-5
Me
Me
H
H
H
Ph(2-CF3)

29-6
Me
Me
H
H
H
Ph(2-F-6-Cl)

29-7
Me
Me
H
Cl
H
Ph(2-F)

29-8
Me
Me
H
Cl
H
Ph(2,6-F2)

29-9
Me
Me
H
Cl
H
ph(2-Cl)

29-10
Me
Me
H
Cl
H
ph(2-Me)

29-11
Me
Me
H
Cl
H
Ph(2-CF3)

29-12
Me
Me
H
Cl
H
Ph(2-F-6-Cl)

29-13
Me
Me
H
Me
H
Ph(2-F)

29-14
Me
Me
H
Me
H
Ph(2,6-F2)

29-15
Me
Me
H
Me
H
Ph(2-Cl)

29-16
Me
Me
H
Me
H
Ph(2-Me)

29-17
Me
Me
H
Me
H
Ph(2-CF3)

29-18
Me
Me
H
Me
H
Ph(2-F-6-Cl)

29-19
Me
Me
H
H
Cl
Ph(2-F)

29-20
Me
Me
H
H
Cl
Ph(2,6-F2)

29-21
Me
Me
H
H
Cl
Ph(2-Cl)

29-22
Me
Me
H
H
Cl
Ph(2-Me)

29-23
Me
Me
H
H
Cl
Ph(2-CF3)

29-24
Me
Me
H
H
Cl
Ph(2-F-6-Cl)

29-25
Me
Me
H
H
Me
Ph(2-F)

29-26
Me
Me
H
H
Me
Ph(2,6-F2)

29-27
Me
Me
H
H
Me
Ph(2-Cl)

29-28
Me
Me
H
H
Me
Ph(2-Me)

29-29
Me
Me
H
H
Me
Ph(2-CF3)

29-30
Me
Me
H
H
Me
Ph(2-F-6-Cl)

29-31
Me
Me
H
Me
Me
Ph(2-F)

29-32
Me
Me
H
Me
Me
Ph(2,6-F2)

29-33
Me
Me
H
Me
Me
Ph(2-Cl)

29-34
Me
Me
H
Me
Me
Ph(2-Me)

29-35
Me
Me
H
Me
Me
Ph(2-CF3)

29-36
Me
Me
H
Me
Me
Ph(2-F-6-Cl)

[0269]

30

TABLE 30

Physical

Compound

properties

No.
R1
R2
R3
X1
X2
B
(mp ° C.)

30-1
Me
Me
H
H
H
Ph(2-F)

30-2
Me
Me
H
H
H
Ph(2,6-F2)

30-3
Me
Me
H
H
H
Ph(2-Cl)

30-4
Me
Me
H
H
H
Ph(2-Me)

30-5
Me
Me
H
H
H
Ph(2-CF3)

30-6
Me
Me
H
H
H
Ph(2-F-6-Cl)

30-7
Me
Me
H
Cl
H
Ph(2-F)

30-8
Me
Me
H
Cl
H
Ph(2,6-F2)

30-9
Me
Me
H
Cl
H
Ph(2-Cl)

30-10
Me
Me
H
Cl
H
Ph(2-Me)

30-11
Me
Me
H
Cl
H
Ph(2-CF3)

30-12
Me
Me
H
Cl
H
Ph(2-F-6-Cl)

30-13
Me
Me
H
Me
H
Ph(2-F)

30-14
Me
Me
H
Me
H
Ph(2,6-F2)

30-15
Me
Me
H
Me
H
Ph(2-Cl)

30-16
Me
Me
H
Me
H
Ph(2-Me)

30-17
Me
Me
H
Me
H
Ph(2-CF3)

30-18
Me
Me
H
Me
H
Ph(2-F-6-Cl)

30-19
Me
Me
H
H
Cl
Ph(2-F)

30-20
Me
Me
H
H
Cl
Ph(2,6-F2)

30-21
Me
Me
H
H
Cl
Ph(2-Cl)

30-22
Me
Me
H
H
Cl
Ph(2-Me)

30-23
Me
Me
H
H
Cl
Ph(2-CF3)

30-24
Me
Me
H
H
Cl
Ph(2-F-6-Cl)

30-25
Me
Me
H
H
Me
Ph(2-F)

30-26
Me
Me
H
H
Me
Ph(2,6-F2)

30-27
Me
Me
H
H
Me
Ph(2-Cl)

30-28
Me
Me
H
H
Me
Ph(2-Me)

30-29
Me
Me
H
H
Me
Ph(2-CF3)

30-30
Me
Me
H
H
Me
Ph(2-F-6-Cl)

30-31
Me
Me
H
Me
Me
Ph(2-F)

30-32
Me
Me
H
Me
Me
Ph(2,6-F2)

30-33
Me
Me
H
Me
Me
Ph(2-Cl)

30-34
Me
Me
H
Me
Me
Ph(2-Me)

30-35
Me
Me
H
Me
Me
Ph(2-CF3)

30-36
Me
Me
H
Me
Me
Ph(2-F-6-Cl)

[0270]

31

TABLE 31

Physical

Compound

properties

No.
R1
R2
R3
X1
X2
B
(mp ° C.)

31-1
Me
Me
H
H
H
Ph(2-F)

31-2
Me
Me
H
H
H
Ph(2,6-F2)

31-3
Me
Me
H
H
H
Ph(2-Cl)

31-4
Me
Me
H
H
H
Ph(2-Me)

31-5
Me
Me
H
H
H
Ph(2-CF3)

31-6
Me
Me
H
H
H
Ph(2-F-6-Cl)

31-7
Me
Me
H
Cl
H
Ph(2-F)

31-8
Me
Me
H
Cl
H
Ph(2,6-F2)

31-9
Me
Me
H
Cl
H
Ph(2-Cl)

31-10
Me
Me
H
Cl
H
Ph(2-Me)

31-11
Me
Me
H
Cl
H
Ph(2-CF3)

31-12
Me
Me
H
Cl
H
Ph(2-F-6-Cl)

31-13
Me
Me
H
Me
H
Ph(2-F)

31-14
Me
Me
H
Me
H
Ph(2,6-F2)

31-15
Me
Me
H
Me
H
Ph(2-Cl)

31-16
Me
Me
H
Me
H
Ph(2-Me)

31-17
Me
Me
H
Me
H
Ph(2-CF3)

31-18
Me
Me
H
Me
H
Ph(2-F-6-Cl)

31-19
Me
Me
H
H
Cl
Ph(2-F)

31-20
Me
Me
H
H
Cl
Ph(2,6-F2)

31-21
Me
Me
H
H
Cl
Ph(2-Cl)

31-22
Me
Me
H
H
Cl
Ph(2-Me)

31-23
Me
Me
H
H
Cl
Ph(2-CF3)

31-24
Me
Me
H
H
Cl
Ph(2-F-6-Cl)

31-25
Me
Me
H
H
Me
Ph(2-F)

31-26
Me
Me
H
H
Me
Ph(2,6-F2)

31-27
Me
Me
H
H
Me
Ph(2-Cl)

31-28
Me
Me
H
H
Me
Ph(2-Me)

31-29
Me
Me
H
H
Me
Ph(2-CF3)

31-30
Me
Me
H
H
Me
Ph(2-F-6-Cl)

31-31
Me
Me
H
Me
Me
Ph(2-F)

31-32
Me
Me
H
Me
Me
Ph(2,6-F2)

31-33
Me
Me
H
Me
Me
Ph(2-Cl)

31-34
Me
Me
H
Me
Me
Ph(2-Me)

31-35
Me
Me
H
Me
Me
Ph(2-CF3)

31-36
Me
Me
H
Me
Me
Ph(2-F-6-Cl)

[0271]

32

TABLE 32

Physical

Compound

properties

No.
R1
R2
R3
X1
X2
(mp ° C.)

32-1
Me
Me
H
H
H
Ph(2-F)

32-2
Me
Me
H
H
H
Ph(2,6-F2)

32-3
Me
Me
H
H
H
Ph(2-Cl)

32-4
Me
Me
H
H
H
Ph(2-Me)

32-5
Me
Me
H
H
H
Ph(2-CF3)

32-6
Me
Me
H
H
H
Ph(2-F-6-Cl)

32-7
Me
Me
H
Cl
H
Ph(2-F)

32-8
Me
Me
H
Cl
H
Ph(2,6-F2)

32-9
Me
Me
H
Cl
H
Ph(2-Cl)

32-10
Me
Me
H
Cl
H
Ph(2-Me)

32-11
Me
Me
H
Cl
H
Ph(2-CF3)

32-12
Me
Me
H
Cl
H
Ph(2-F-6-Cl)

32-13
Me
Me
H
Me
H
Ph(2-F)

32-14
Me
Me
H
Me
H
Ph(2,6-F2)

32-15
Me
Me
H
Me
H
Ph(2-Cl)

32-16
Me
Me
H
Me
H
Ph(2-Me)

32-17
Me
Me
H
Me
H
Ph(2-CF3)

32-18
Me
Me
H
Me
H
Ph(2-F-6-Cl)

32-19
Me
Me
H
H
Cl
Ph(2-F)

32-20
Me
Me
H
H
Cl
Ph(2,6-F2)

32-21
Me
Me
H
H
Cl
Ph(2-Cl)

32-22
Me
Me
H
H
Cl
Ph(2-Me)

32-23
Me
Me
H
H
Cl
Ph(2-CF3)

32-24
Me
Me
H
H
Cl
Ph(2-F-6-Cl)

32-25
Me
Me
H
H
Me
Ph(2-F)

32-26
Me
Me
H
H
Me
Ph(2,6-F2)

32-27
Me
Me
H
H
Me
Ph(2-Cl)

32-28
Me
Me
H
H
Me
Ph(2-Me)

32-29
Me
Me
H
H
Me
Ph(2-CF3)

32-30
Me
Me
H
H
Me
Ph(2-F-6-Cl)

32-31
Me
Me
H
Me
Me
Ph(2-F)

32-32
Me
Me
H
Me
Me
Ph(2,6-F2)

32-33
Me
Me
H
Me
Me
Ph(2-Cl)

32-34
Me
Me
H
Me
Me
Ph(2-Me)

32-35
Me
Me
H
Me
Me
Ph(2-CF3)

32-36
Me
Me
H
Me
Me
Ph(2-F-6-Cl)

[0272]

33

TABLE 33

Physical

Compound

properties

No.
R1
R2
R3
X
B
(mp ° C.)

33-1
Me
Me
H
H
Ph(2-F)

33-2
Me
Me
H
H
Ph(2,6-F2)

33-3
Me
Me
H
H
Ph(2-Cl)

33-4
Me
Me
H
H
Ph(2-Me)

33-5
Me
Me
H
H
Ph(2-CF3)

33-6
Me
Me
H
H
Ph(2-F-6-Cl)

33-7
Me
Me
H
Cl
Ph(2-F)

33-8
Me
Me
H
Cl
Ph(2,6-F2)

33-9
Me
Me
H
Cl
Ph(2-Cl)

33-10
Me
Me
H
Cl
Ph(2-Me)

33-11
Me
Me
H
Cl
Ph(2-CF3)

33-12
Me
Me
H
Cl
Ph(2-F-6-Cl)

33-13
Me
Me
H
Br
Ph(2-F)

33-14
Me
Me
H
Br
Ph(2,6-F2)

33-15
Me
Me
H
Br
Ph(2-Cl)

33-16
Me
Me
H
Br
Ph(2-Me)

33-17
Me
Me
H
Br
Ph(2-CF3)

33-18
Me
Me
H
Br
Ph(2-F-6-Cl)

33-19
Me
Me
H
Me
Ph(2-F)

33-20
Me
Me
H
Me
Ph(2,6-F2)

33-21
Me
Me
H
Me
Ph(2-Cl)

33-22
Me
Me
H
Me
Ph(2-Me)

33-23
Me
Me
H
Me
Ph(2-CF3)

33-24
Me
Me
H
Me
Ph(2-F-6-Cl)

33-25
Me
Me
H
Et
Ph(2-F)

33-26
Me
Me
H
Et
Ph(2,6-F2)

33-27
Me
Me
H
Et
Ph(2-Cl)

33-28
Me
Me
H
Et
Ph(2-Me)

33-29
Me
Me
H
Et
Ph(2-CF3)

33-30
Me
Me
H
Et
Ph(2-F-6-Cl)

[0273]

34

TABLE 34

Physical

Compound

properties

No.
R1
R2
R3
X
B
(mp ° C.)

34-1
Me
Me
H
H
Ph(2-F)

34-2
Me
Me
H
H
Ph(2,6-F2)

34-3
Me
Me
H
H
Ph(2-Cl)

34-4
Me
Me
H
H
Ph(2-Me)

34-5
Me
Me
H
H
Ph(2-CF3)

34-6
Me
Me
H
H
Ph(2-F-6-Cl)

34-7
Me
Me
H
Cl
Ph(2-F)

34-8
Me
Me
H
Cl
Ph(2,6-F2)

34-9
Me
Me
H
Cl
Ph(2-Cl)

34-10
Me
Me
H
Cl
Ph(2-Me)

34-11
Me
Me
H
Cl
Ph(2-CF3)

34-12
Me
Me
H
Cl
Ph(2-F-6-Cl)

34-13
Me
Me
H
Br
Ph(2-F)

34-14
Me
Me
H
Br
Ph(2,6-F2)

34-15
Me
Me
H
Br
Ph(2-Cl)

34-16
Me
Me
H
Br
Ph(2-Me)

34-17
Me
Me
H
Br
Ph(2-CF3)

34-18
Me
Me
H
Br
Ph(2-F-6-Cl)

34-19
Me
Me
H
Me
Ph(2-F)

34-20
Me
Me
H
Me
Ph(2,6-F2)

34-21
Me
Me
H
Me
Ph(2-Cl)

34-22
Me
Me
H
Me
Ph(2-Me)

34-23
Me
Me
H
Me
Ph(2-CF3)

34-24
Me
Me
H
Me
Ph(2-F-6-Cl)

34-25
Me
Me
H
Et
Ph(2-F)

34-26
Me
Me
H
Et
Ph(2,6-F2)

34-27
Me
Me
H
Et
Ph(2-Cl)

34-28
Me
Me
H
Et
Ph(2-Me)

34-29
Me
Me
H
Et
Ph(2-CF3)

34-30
Me
Me
H
Et
Ph(2-F-6-Cl)

[0274]

35

TABLE 35

Physical

Compound

properties

No.
R1
R2
R3
X
B
(mp ° C.)

35-1
Me
Me
H
H
Ph(2-F)

35-2
Me
Me
H
H
Ph(2,6-F2)

35-3
Me
Me
H
H
Ph(2-Cl)

35-4
Me
Me
H
H
Ph(2-Me)

35-5
Me
Me
H
H
Ph(2-CF3)

35-6
Me
Me
H
H
Ph(2-F-6-Cl)

35-7
Me
Me
H
Cl
Ph(2-F)

35-8
Me
Me
H
Cl
Ph(2,6-F2)

35-9
Me
Me
H
Cl
Ph(2-Cl)

35-10
Me
Me
H
Cl
Ph(2-Me)

35-11
Me
Me
H
Cl
Ph(2-CF3)

35-12
Me
Me
H
Cl
Ph(2-F-6-Cl)

35-13
Me
Me
H
Br
Ph(2-F)

35-14
Me
Me
H
Br
Ph(2,6-F2)

35-15
Me
Me
H
Br
Ph(2-Cl)

35-16
Me
Me
H
Br
Ph(2-Me)

35-17
Me
Me
H
Br
Ph(2-CF3)

35-18
Me
Me
H
Br
Ph(2-F-6-Cl)

35-19
Me
Me
H
Me
Ph(2-F)

35-20
Me
Me
H
Me
Ph(2,6-F2)

35-21
Me
Me
H
Me
Ph(2-Cl)

35-22
Me
Me
H
Me
Ph(2-Me)

35-23
Me
Me
H
Me
Ph(2-CF3)

35-24
Me
Me
H
Me
Ph(2-F-6-Cl)

35-25
Me
Me
H
Et
Ph(2-F)

35-26
Me
Me
H
Et
Ph(2,6-F2)

35-27
Me
Me
H
Et
Ph(2-Cl)

35-28
Me
Me
H
Et
Ph(2-Me)

35-29
Me
Me
H
Et
Ph(2-CF3)

35-30
Me
Me
H
Et
Ph(2-F-6-Cl)

[0275]

36

TABLE 36

Physical

Compound

properties

No.
R1
R2
R3
X
B
(mp ° C.)

36-1
Me
Me
H
H
Ph(2-F)

36-2
Me
Me
H
H
Ph(2,6-F2)

36-3
Me
Me
H
H
Ph(2-Cl)

36-4
Me
Me
H
H
Ph(2-Me)

36-5
Me
Me
H
H
Ph(2-CF3)

36-6
Me
Me
H
H
Ph(2-F-6-Cl)

36-7
Me
Me
H
Cl
Ph(2-F)

36-8
Me
Me
H
Cl
Ph(2,6-F2)

36-9
Me
Me
H
Cl
Ph(2-Cl)

36-10
Me
Me
H
Cl
Fh(2-Me)

36-11
Me
Me
H
Cl
Ph(2-CF3)

36-12
Me
Me
H
Cl
Ph(2-F-6-Cl)

36-13
Me
Me
H
Br
Ph(2-F)

36-14
Me
Me
H
Br
Ph(2,6-F2)

36-15
Me
Me
H
Br
Ph(2-Cl)

36-16
Me
Me
H
Br
Ph(2-Me)

36-17
Me
Me
H
Br
Ph(2-CF3)

36-18
Me
Me
H
Br
Ph(2-F-6-Cl)

36-19
Me
Me
H
Me
Ph(2-F)

36-20
Me
Me
H
Me
Ph(2,6-F2)

36-21
Me
Me
H
Me
Ph(2-Cl)

36-22
Me
Me
H
Me
Ph(2-Me)

36-23
Me
Me
H
Me
Ph(2-CF3)

36-24
Me
Me
H
Me
Ph(2-F-6-Cl)

36-25
Me
Me
H
Et
Ph(2-F)

36-26
Me
Me
H
Et
Ph(2,6-F2)

36-27
Me
Me
H
Et
Ph(2-Cl)

36-28
Me
Me
H
Et
Ph(2-Me)

36-29
Me
Me
H
Et
Ph(2-CF3)

36-30
Me
Me
H
Et
Ph(2-F-6-Cl)

[0276]

37

TABLE 37

Physical

Compound

properties

No.
R1
R2
R3
X
B
(mp ° C.)

37-1
Me
Me
H
H
Ph(2-F)

37-2
Me
Me
H
H
Ph(2,6-F2)

37-3
Me
Me
H
H
Ph(2-Cl)

37-4
Me
Me
H
H
Ph(2-Me)

37-5
Me
Me
H
H
Ph(2-CF3)

37-6
Me
Me
H
H
Ph(2-F-6-Cl)

37-7
Me
Me
H
Cl
Ph(2-F)

37-8
Me
Me
H
Cl
Ph(2,6-F2)

37-9
Me
Me
H
Cl
Ph(2-Cl)

37-10
Me
Me
H
Cl
Ph(2-Me)

37-11
Me
Me
H
Cl
Ph(2-CF3)

37-12
Me
Me
H
Cl
Ph(2-F-6-Cl)

37-13
Me
Me
H
Br
Ph(2-F)

37-14
Me
Me
H
Br
Ph(2,6-F2)

37-15
Me
Me
H
Br
Ph(2-Cl)

37-16
Me
Me
H
Br
Ph(2-Me)

37-17
Me
Me
H
Br
Ph(2-CF3)

37-18
Me
Me
H
Br
Ph(2-F-6-Cl)

37-19
Me
Me
H
Me
Ph(2-F)

37-20
Me
Me
H
Me
Ph(2,6-F2)

37-21
Me
Me
H
Me
Ph(2-Cl)

37-22
Me
Me
H
Me
Ph(2-Me)

37-23
Me
Me
H
Me
Ph(2-CF3)

37-24
Me
Me
H
Me
Ph(2-F-6-Cl)

37-25
Me
Me
H
Et
Ph(2-F)

37-26
Me
Me
H
Et
Ph(2,6-F2)

37-27
Me
Me
H
Et
Ph(2-Cl)

37-28
Me
Me
H
Et
Ph(2-Me)

37-29
Me
Me
H
Et
Ph(2-CF3)

37-30
Me
Me
H
Et
Ph(2-F-6-Cl)

[0277]

38

TABLE 38

Physical

Compound

properties

No.
R1
R2
R3
X
B
(mp ° C.)

38-1
Me
Me
H
H
Ph(2-F)

38-2
Me
Me
H
H
Ph(2,6-F2)

38-3
Me
Me
H
H
Ph(2-Cl)

38-4
Me
Me
H
H
Ph(2-Me)

38-5
Me
Me
H
H
Ph(2-CF3)

38-6
Me
Me
H
H
Ph(2-F-6-Cl)

38-7
Me
Me
H
Cl
Ph(2-F)

38-8
Me
Me
H
Cl
Ph(2,6-F2)

38-9
Me
Me
H
Cl
Ph(2-Cl)

38-10
Me
Me
H
Cl
Ph(2-Me)

38-11
Me
Me
H
Cl
Ph(2-CF3)

38-12
Me
Me
H
Cl
Ph(2-F-6-Cl)

38-13
Me
Me
H
Br
Ph(2-F)

38-14
Me
Me
H
Br
Ph(2,6-F2)

38-15
Me
Me
H
Br
Ph(2-Cl)

38-16
Me
Me
H
Br
Ph(2-Me)

38-17
Me
Me
H
Br
Ph(2-CF3)

38-18
Me
Me
H
Br
Ph(2-F-6-Cl)

38-19
Me
Me
H
Me
Ph(2-F)

38-20
Me
Me
H
Me
Ph(2,6-F2)

38-21
Me
Me
H
Me
Ph(2-Cl)

38-22
Me
Me
H
Me
Ph(2-Me)

38-23
Me
Me
H
Me
Ph(2-CF3)

38-24
Me
Me
H
Me
Ph(2-F-6-Cl)

38-25
Me
Me
H
Et
Ph(2-F)

38-26
Me
Me
H
Et
Ph(2,6-F2)

38-27
Me
Me
H
Et
Ph(2-Cl)

38-28
Me
Me
H
Et
Ph(2-Me)

38-29
Me
Me
H
Et
Ph(2-CF3)

38-30
Me
Me
H
Et
Ph(2-F-6-Cl)

[0278]

39

TABLE 39

Physical

Compound

properties

No.
R1
R2
R3
X
B
(mp ° C.)

39-1
Me
Me
H
H
Ph(2-F)

39-2
Me
Me
H
H
Ph(2,6-F2)

39-3
Me
Me
H
H
Ph(2-Cl)

39-4
Me
Me
H
H
Ph(2-Me)

39-5
Me
Me
H
H
Ph(2-CF3)

39-6
Me
Me
H
H
Ph(2-F-6-Cl)

39-7
Me
Me
H
Cl
Ph(2-F)

39-8
Me
Me
H
Cl
Ph(2,6-F2)

39-9
Me
Me
H
Cl
Ph(2-Cl)

39-10
Me
Me
H
Cl
Ph(2-Me)

39-11
Me
Me
H
Cl
Ph(2-CF3)

39-12
Me
Me
H
Cl
Ph(2-F-6-Cl)

39-13
Me
Me
H
Br
Ph(2-F)

39-14
Me
Me
H
Br
Ph(2,6-F2)

39-15
Me
Me
H
Br
Ph(2-Cl)

39-16
Me
Me
H
Br
Ph(2-Me)

39-17
Me
Me
H
Br
Ph(2-CF3)

39-18
Me
Me
H
Br
Ph(2-F-6-Cl)

39-19
Me
Me
H
Me
Ph(2-F)

39-20
Me
Me
H
Me
Ph(2,6-F2)

39-21
Me
Me
H
Me
Ph(2-Cl)

39-22
Me
Me
H
Me
Ph(2-Me)

39-23
Me
Me
H
Me
Ph(2-CF3)

39-24
Me
Me
H
Me
Ph(2-F-6-Cl)

39-25
Me
Me
H
Et
Ph(2-F)

39-26
Me
Me
H
Et
Ph(2,6-F2)

39-27
Me
Me
H
Et
Ph(2-Cl)

39-28
Me
Me
H
Et
Ph(2-Me)

39-29
Me
Me
H
Et
Ph(2-CF3)

39-30
Me
Me
H
Et
Ph(2-F-6-Cl)

[0279]

40

TABLE 40

Physical

Compound

properties

No.
R1
R2
R3
X
B
(mp ° C.)

40-1
Me
Me
H
H
H
Ph(2-F)

40-2
Me
Me
H
H
H
Ph(2,6-F2)

40-3
Me
Me
H
H
H
Ph(2-Cl)

40-4
Me
Me
H
H
H
Ph(2-Me)

40-5
Me
Me
H
H
H
Ph(2-CF3)

40-6
Me
Me
H
H
H
Ph(2-F-6-Cl)

40-7
Me
Me
H
Cl
H
Ph(2-F)

40-8
Me
Me
H
Cl
H
Ph(2,6-F2)

40-9
Me
Me
H
Cl
H
Ph(2-Cl)

40-10
Me
Me
H
Cl
H
Ph(2-Me)

40-11
Me
Me
H
Cl
H
Ph(2-CF3)

40-12
Me
Me
H
Cl
H
Ph(2-F-6-Cl)

40-13
Me
Me
H
Me
H
Ph(2-F)

40-14
Me
Me
H
Me
H
Ph(2,6-F2)

40-15
Me
Me
H
Me
H
Ph(2-Cl)

40-16
Me
Me
H
Me
H
Ph(2-Me)

40-17
Me
Me
H
Me
H
Ph(2-CF3)

40-18
Me
Me
H
Me
H
Ph(2-F-6-Cl)

40-19
Me
Me
H
H
Cl
Ph(2-F)

40-20
Me
Me
H
H
Cl
Ph(2,6-F2)

40-21
Me
Me
H
H
Cl
Ph(2-Cl)

40-22
Me
Me
H
H
Cl
Ph(2-Me)

40-23
Me
Me
H
H
Cl
Ph(2-CF3)

40-24
Me
Me
H
H
Cl
Ph(2-F-6-Cl)

40-25
Me
Me
H
H
Me
Ph(2-F)

40-26
Me
Me
H
H
Me
Ph(2,6-F2)

40-27
Me
Me
H
H
Me
Ph(2-Cl)

40-28
Me
Me
H
H
Me
Ph(2-Me)

40-29
Me
Me
H
H
Me
Ph(2-CF3)

40-30
Me
Me
H
H
Me
Ph(2-F-6-Cl)

40-31
Me
Me
H
Me
Me
Ph(2-F)

40-32
Me
Me
H
Me
Me
Ph(2,6-F2)

40-33
Me
Me
H
Me
Me
Ph(2-Cl)

40-34
Me
Me
H
Me
Me
Ph(2-Me)

40-35
Me
Me
H
Me
Me
Ph(2-CF3)

40-36
Me
Me
H
Me
Me
Ph(2-F-6-Cl)

[0280]

41

TABLE 41

Physical

Compound

properties

No.
R1
R2
R3
X
B
(mp ° C.)

41-1
Me
Me
H
H
H
Ph(2-F)

41-2
Me
Me
H
H
H
Ph(2,6-F2)

41-3
Me
Me
H
H
H
Ph(2-Cl)

41-4
Me
Me
H
H
H
Ph(2-Me)

41-5
Me
Me
H
H
H
Ph(2-CF3)

41-6
Me
Me
H
H
H
Ph(2-F-6-Cl)

41-7
Me
Me
H
Cl
H
Ph(2-F)

41-8
Me
Me
H
Cl
H
Ph(2,6-F2)

41-9
Me
Me
H
Cl
H
Ph(2-Cl)

41-10
Me
Me
H
Cl
H
Ph(2-Me)

41-11
Me
Me
H
Cl
H
Ph(2-CF3)

41-12
Me
Me
H
Cl
H
Ph(2-F-6-Cl)

41-13
Me
Me
H
Me
H
Ph(2-F)

41-14
Me
Me
H
Me
H
Ph(2,6-F2)

41-15
Me
Me
H
Me
H
Ph(2-Cl)

41-16
Me
Me
H
Me
H
Ph(2-Me)

41-17
Me
Me
H
Me
H
Ph(2-CF3)

41-18
Me
Me
H
Me
H
Ph(2-F-6-Cl)

41-19
Me
Me
H
H
Cl
Ph(2-F)

41-20
Me
Me
H
H
Cl
Ph(2,6-F2)

41-21
Me
Me
H
H
Cl
Ph(2-Cl)

41-22
Me
Me
H
H
Cl
Ph(2-Me)

41-23
Me
Me
H
H
Cl
Ph(2-CF3)

41-24
Me
Me
H
H
Cl
Ph(2-F-6-Cl)

41-25
Me
Me
H
H
Me
Ph(2-F)

41-26
Me
Me
H
H
Me
Ph(2,6-F2)

41-27
Me
Me
H
H
Me
Ph(2-Cl)

41-28
Me
Me
H
H
Me
Ph(2-Me)

41-29
Me
Me
H
H
Me
Ph(2-CF3)

41-30
Me
Me
H
H
Me
Ph(2-F-6-Cl)

41-31
Me
Me
H
Me
Me
Ph(2-F)

41-32
Me
Me
H
Me
Me
Ph(2,6-F2)

41-33
Me
Me
H
Me
Me
Ph(2-Cl)

41-34
Me
Me
H
Me
Me
Ph(2-Me)

41-35
Me
Me
H
Me
Me
Ph(2-CF3)

41-36
Me
Me
H
Me
Me
Ph(2-F-6-Cl)

[0281]

42

TABLE 42

Physical

Compound

properties

No.
R1
R2
R3
X1
X2
X3
B
(mp ° C.)

42-1
Me
Me
H
H
H
H
Ph(2-F)

42-2
Me
Me
H
H
H
H
Ph(2,6-F2)

42-3
Me
Me
H
H
H
H
Ph(2-Cl)

42-4
Me
Me
H
H
H
H
Ph(2-Me)

42-5
Me
Me
H
H
H
H
Ph(2-CF3)

42-6
Me
Me
H
H
H
H
Ph(2-F-6-Cl)

42-7
Me
Me
H
H
Cl
H
Ph(2-F)

42-8
Me
Me
H
H
Cl
H
Ph(2,6-F2)

42-9
Me
Me
H
H
Cl
H
Ph(2-Cl)

42-10
Me
Me
H
H
Cl
H
Ph(2-Me)

42-11
Me
Me
H
H
Cl
H
Ph(2-CF3)

42-12
Me
Me
H
H
Cl
H
Ph(2-F-6-Cl)

42-13
Me
Me
H
H
Me
H
Ph(2-F)

42-14
Me
Me
H
H
Me
H
Ph(2,6-F2)

42-15
Me
Me
H
H
Me
H
Ph(2-Cl)

42-16
Me
Me
H
H
Me
H
Ph(2-Me)

42-17
Me
Me
H
H
Me
H
Ph(2-CF3)

42-18
Me
Me
H
H
Me
H
Ph(2-F-6-Cl)

42-19
Me
Me
H
H
H
Me
Ph(2-F)

42-20
Me
Me
H
H
H
Me
Ph(2,6 F2)

42-21
Me
Me
H
H
H
Me
Ph(2-Cl)

42-22
Me
Me
H
H
H
Me
Ph(2-Me)

42-23
Me
Me
H
H
H
Me
Ph(2-CF3)

42-24
Me
Me
H
H
H
Me
Ph(2-F-6-Cl)

42-25
Me
Me
H
Me
H
H
Ph(2-F)

42-26
Me
Me
H
Me
H
H
Ph(2,6-F2)

42-27
Me
Me
H
Me
H
H
Ph(2-Cl)

42-28
Me
Me
H
Me
H
H
Ph(2-Me)

42-29
Me
Me
H
Me
H
H
Ph(2-CF3)

42-30
Me
Me
H
Me
H
H
Ph(2-F-6-Cl)

42-31
Me
Me
H
Me
Cl
H
Ph(2-F)

42-32
Me
Me
H
Me
Cl
H
Ph(2,6-F2)

42-33
Me
Me
H
Me
Cl
H
Ph(2-Cl)

42-34
Me
Me
H
Me
Cl
H
Ph(2-Me)

42-35
Me
Me
H
Me
Cl
H
Ph(2-CF3)

42-36
Me
Me
H
Me
Cl
H
Ph(2-F-6-Cl)

42-37
Me
Me
H
Me
Me
H
Ph(2-F)

42-38
Me
Me
H
Me
Me
H
Ph(2,6-F2)

42-39
Me
Me
H
Me
Me
H
Ph(2-Cl)

42-40
Me
Me
H
Me
Me
H
Ph(2-Me)

42-41
Me
Me
H
Me
Me
H
Ph(2-CF3)

42-42
Me
Me
H
Me
Me
H
Ph(2-F-6-Cl)

42-43
Me
Me
H
Me
H
Me
Ph(2-F)

42-44
Me
Me
H
Me
H
Me
Ph(2,6-F2)

42-45
Me
Me
H
Me
H
Me
Ph(2-Cl)

42-46
Me
Me
H
Me
H
Me
Ph(2-Me)

42-47
Me
Me
H
Me
H
Me
Ph(2-CF3)

42-48
Me
Me
H
Me
H
Me
Ph(2-F-6-Cl)

[0282]

43

TABLE 42

Physical

Compound

properties

No.
R1
R2
R3
X1
X2
X3
B
(mp ° C.)

43-1
Me
Me
H
H
H
H
Ph(2-F)

43-2
Me
Me
H
H
H
H
Ph(2,6-F2)

43-3
Me
Me
H
H
H
H
Ph(2-Cl)

43-4
Me
Me
H
H
H
H
Ph(2-Me)

43-5
Me
Me
H
H
H
H
Ph(2-CF3)

43-6
Me
Me
H
H
H
H
Ph(2-F-6-Cl)

43-7
Me
Me
H
H
Cl
H
Ph(2-F)

43-8
Me
Me
H
H
Cl
H
Ph(2,6-F2)

43-9
Me
Me
H
H
Cl
H
Ph(2-Cl)

43-10
Me
Me
H
H
Cl
H
Ph(2-Me)

43-11
Me
Me
H
H
Cl
H
Ph(2-CF3)

43-12
Me
Me
H
H
Cl
H
Ph(2-F-6-Cl)

43-13
Me
Me
H
H
Me
H
Ph(2-F)

43-14
Me
Me
H
H
Me
H
Ph(2,6-F2)

43-15
Me
Me
H
H
Me
H
Ph(2-Cl)

43-16
Me
Me
H
H
Me
H
Ph(2-Me)

43-17
Me
Me
H
H
Me
H
Ph(2-CF3)

43-18
Me
Me
H
H
Me
H
Ph(2-F-6-Cl)

43-19
Me
Me
H
H
H
Me
Ph(2-F)

43-20
Me
Me
H
H
H
Me
Ph(2,6-F2)

43-21
Me
Me
H
H
H
Me
Ph(2-Cl)

43-22
Me
Me
H
H
H
Me
Ph(2-Me)

43-23
Me
Me
H
H
H
Me
Ph(2-CF3)

43-24
Me
Me
H
H
H
Me
Ph(2-F-6-Cl)

43-25
Me
Me
H
Me
H
H
Ph(2-F)

43-26
Me
Me
H
Me
H
H
Ph(2,6-F2)

43-27
Me
Me
H
Me
H
H
Ph(2-Cl)

43-28
Me
Me
H
Me
H
H
Ph(2-Me)

43-29
Me
Me
H
Me
H
H
Ph(2-CF3)

43-30
Me
Me
H
Me
H
H
Ph(2-F-6-Cl)

43-31
Me
Me
H
Me
Cl
H
Ph(2-F)

43-32
Me
Me
H
Me
Cl
H
Ph(2,6-F2)

43-33
Me
Me
H
Me
Cl
H
Ph(2-Cl)

43-34
Me
Me
H
Me
Cl
H
Ph(2-Me)

43-35
Me
Me
H
Me
Cl
H
Ph(2-CF3)

43-36
Me
Me
H
Me
Cl
H
Ph(2-F-6-Cl)

43-37
Me
Me
H
Me
Me
H
Ph(2-F)

43-38
Me
Me
H
Me
Me
H
Ph(2,6-F2)

43-39
Me
Me
H
Me
Me
H
Ph(2-Cl)

43-40
Me
Me
H
Me
Me
H
Ph(2-Me)

43-41
Me
Me
H
Me
Me
H
Ph(2-CF3)

43-42
Me
Me
H
Me
Me
H
Ph(2-F-6-Cl)

43-43
Me
Me
H
Me
H
Me
Ph(2-F)

43-44
Me
Me
H
Me
H
Me
Ph(2,6-F2)

43-45
Me
Me
H
Me
H
Me
Ph(2-Cl)

43-46
Me
Me
H
Me
H
Me
Ph(2-Me)

43-47
Me
Me
H
Me
H
Me
Ph(2-CF3)

43-48
Me
Me
H
Me
H
Me
Ph(2-F-6-Cl)

[0283]

44

TABLE 44

Physical

Compound

properties

No.
R1
R2
R3
X1
X2
X3
B
(mp ° C.)

44-1
Me
Me
H
H
H
H
Ph(2-F)

44-2
Me
Me
H
H
H
H
Ph(2,6-F2)

44-3
Me
Me
H
H
H
H
Ph(2-Cl)

44-4
Me
Me
H
H
H
H
Ph(2-Me)

44-5
Me
Me
H
H
H
H
Ph(2-CF3)

44-6
Me
Me
H
H
H
H
Ph(2-F-6-Cl)

44-7
Me
Me
H
H
Cl
H
Ph(2-F)

44-8
Me
Me
H
H
Cl
H
Ph(2,6-F2)

44-9
Me
Me
H
H
Cl
H
Ph(2-Cl)

44-10
Me
Me
H
H
Cl
H
Ph(2-Me)

44-11
Me
Me
H
H
Cl
H
Ph(2-CF3)

44-12
Me
Me
H
H
Cl
H
Ph(2-F-6-Cl)

44-13
Me
Me
H
H
Me
H
Ph(2-F)

44-14
Me
Me
H
H
Me
H
Ph(2,6-F2)

44-15
Me
Me
H
H
Me
H
Ph(2-Cl)

44-16
Me
Me
H
H
Me
H
Ph(2-Me)

44-17
Me
Me
H
H
Me
H
Ph(2-CF3)

44-18
Me
Me
H
H
Me
H
Ph(2-F-6-Cl)

44-19
Me
Me
H
H
H
Me
Ph(2-F)

44-20
Me
Me
H
H
H
Me
Ph(2,6-F2)

44-21
Me
Me
H
H
H
Me
Ph(2-Cl)

44-22
Me
Me
H
H
H
Me
Ph(2-Me)

44-23
Me
Me
H
H
H
Me
Ph(2-CF3)

44-24
Me
Me
H
H
H
Me
Ph(2-F-6-Cl)

44-25
Me
Me
H
Me
H
H
Ph(2-F)

44-26
Me
Me
H
Me
H
H
Ph(2,6-F2)

44-27
Me
Me
H
Me
H
H
Ph(2-Cl)

44-28
Me
Me
H
Me
H
H
Ph(2-Me)

44-29
Me
Me
H
Me
H
H
Ph(2-CF3)

44-30
Me
Me
H
Me
H
H
Ph(2-F-6-Cl)

44-31
Me
Me
H
Me
Cl
H
Ph(2-F)

44-32
Me
Me
H
Me
Cl
H
Ph(2,6-F2)

44-33
Me
Me
H
Me
Cl
H
Ph(2-Cl)

44-34
Me
Me
H
Me
Cl
H
Ph(2-Me)

44-35
Me
Me
H
Me
Cl
H
Ph(2-CF2)

44-36
Me
Me
H
Me
Cl
H
Ph(2-F-6-Cl)

44-37
Me
Me
H
Me
Me
H
Ph(2-F)

44-38
Me
Me
H
Me
Me
H
Ph(2,6-F2)

44-39
Me
Me
H
Me
Me
H
Ph(2-Cl)

44-40
Me
Me
H
Me
Me
H
Ph(2-Me)

44-41
Me
Me
H
Me
Me
H
Ph(2-CF3)

44-42
Me
Me
H
Me
Me
H
Ph(2-F-6-Cl)

44-43
Me
Me
H
Me
H
Me
Ph(2-F)

44-44
Me
Me
H
Me
H
Me
Ph(2,6-F2)

44-45
Me
Me
H
Me
H
Me
Ph(2-Cl)

44-46
Me
Me
H
Me
H
Me
Ph(2-Me)

44-47
Me
Me
H
Me
H
Me
Ph(2-CF3)

44-48
Me
Me
H
Me
H
Me
Ph(2-F-6-Cl)

[0284]

Physical

Compound

properties

No.
R1
R2
R3
X1
X2
B
(mp ° C.)

45-1
Me
Me
H
H
H
Ph(2-F)

45-2
Me
Me
H
H
H
Ph(2,6-F2)

45-3
Me
Me
H
H
H
Ph(2-Cl)

45-4
Me
Me
H
H
H
Ph(2-Me)

45-5
Me
Me
H
H
H
Ph(2-CF3)

45-6
Me
Me
H
H
H
Ph(2-F-6-Cl)

45-7
Me
Me
H
Cl
H
Ph(2-F)

45-8
Me
Me
H
Cl
H
Ph(2,6-F2)

45-9
Me
Me
H
Cl
H
Ph(2-Cl)

45-10
Me
Me
H
Cl
H
Ph(2-Me)

45-11
Me
Me
H
Cl
H
Ph(2-CF3)

45-12
Me
Me
H
Cl
H
Ph(2-F-6-Cl)

45-13
Me
Me
H
Me
H
Ph(2-F)

45-14
Me
Me
H
Me
H
Ph(2,6-F2)

45-15
Me
Me
H
Me
H
Ph(2-Cl)

45-16
Me
Me
H
Me
H
Ph(2-Me)

45-17
Me
Me
H
Me
H
Ph(2-CF3)

45-18
Me
Me
H
Me
H
Ph(2-F-6-Cl)

45-19
Me
Me
H
H
Cl
Ph(2-F)

45-20
Me
Me
H
H
Cl
Ph(2,6-F2)

45-21
Me
Me
H
H
Cl
Ph(2-Cl)

45-22
Me
Me
H
H
Cl
Ph(2-Me)

45-23
Me
Me
H
H
Cl
Ph(2-CF3)

45-24
Me
Me
H
H
Cl
Ph(2-F-6-Cl)

45-25
Me
Me
H
H
Me
Ph(2-F)

45-26
Me
Me
H
H
Me
Ph(2,6-F2)

45-27
Me
Me
H
H
Me
Ph(2-Cl)

45-28
Me
Me
H
H
Me
Ph(2-Me)

45-29
Me
Me
H
H
Me
Ph(2-CF3)

45-30
Me
Me
H
H
Me
Ph(2-F-6-Cl)

45-31
Me
Me
H
Me
Me
Ph(2-F)

45-32
Me
Me
H
Me
Me
Ph(2,6-F2)

45-33
Me
Me
H
Me
Me
Ph(2-Cl)

45-34
Me
Me
H
Me
Me
Ph(2-Me)

45-35
Me
Me
H
Me
Me
Ph(2-CF3)

45-36
Me
Me
H
Me
Me
Ph(2-F-6-Cl)

[0285]

46

TABLE 46

Physical

Compound

properties

No.
R1
R2
R3
X1
X2
X3
B
(mp ° C.)

46-1
Me
Me
H
H
H
H
Ph(2-F)

46-2
Me
Me
H
H
H
H
Ph(2,6-F2)

46-3
Me
Me
H
H
H
H
Ph(2-Cl)

46-4
Me
Me
H
H
H
H
Ph(2-Me)

46-5
Me
Me
H
H
H
H
Ph(2-CF3)

46-6
Me
Me
H
H
H
H
Ph(2-F-6-Cl)

46-7
Me
Me
H
H
Cl
H
Ph(2-F)

46-8
Me
Me
H
H
Cl
H
Ph(2,6-F2)

46-9
Me
Me
H
H
Cl
H
Ph(2-Cl)

46-10
Me
Me
H
H
Cl
H
Ph(2-Me)

46-11
Me
Me
H
H
Cl
H
Ph(2-CF3)

46-12
Me
Me
H
H
Cl
H
Ph(2-F-6-Cl)

46-13
Me
Me
H
H
Me
H
Ph(2-F)

46-14
Me
Me
H
H
Me
H
Ph(2,6-F2)

46-15
Me
Me
H
H
Me
H
Ph(2-Cl)

46-16
Me
Me
H
H
Me
H
Ph(2-Me)

46-17
Me
Me
H
H
Me
H
Ph(2-CF3)

46-18
Me
Me
H
H
Me
H
Ph(2-F-6-Cl)

46-19
Me
Me
H
H
H
Me
Ph(2-F)

46-20
Me
Me
H
H
H
Me
Ph(2,6-F2)

46-21
Me
Me
H
H
H
Me
Ph(2-Cl)

46-22
Me
Me
H
H
H
Me
Ph(2-Me)

46-23
Me
Me
H
H
H
Me
Ph(2-CF3)

46-24
Me
Me
H
H
H
Me
Ph(2-F-6-Cl)

46-25
Me
Me
H
Me
H
H
Ph(2-F)

46-26
Me
Me
H
Me
H
H
Ph(2,6-F2)

46-27
Me
Me
H
Me
H
H
Ph(2-Cl)

46-28
Me
Me
H
Me
H
H
Ph(2-Me)

46-29
Me
Me
H
Me
H
H
Ph(2-CF3)

46-30
Me
Me
H
Me
H
H
Ph(2-F-6-Cl)

46-31
Me
Me
H
Me
Cl
H
Ph(2-F)

46-32
Me
Me
H
Me
Cl
H
Ph(2,6-F2)

46-33
Me
Me
H
Me
Cl
H
Ph(2-Cl)

46-34
Me
Me
H
Me
Cl
H
Ph(2-Me)

46-35
Me
Me
H
Me
Cl
H
Ph(2-CF3)

46-36
Me
Me
H
Me
Cl
H
Ph(2-F-6-Cl)

46-37
Me
Me
H
Me
Me
H
Ph(2-F)

46-38
Me
Me
H
Me
Me
H
Ph(2,6-F2)

46-39
Me
Me
H
Me
Me
H
Ph(2-Cl)

46-40
Me
Me
H
Me
Me
H
Ph(2-Me)

46-41
Me
Me
H
Me
Me
H
Ph(2-CF3)

46-42
Me
Me
H
Me
Me
H
Ph(2-F-6-Cl)

46-43
Me
Me
H
Me
H
Me
Ph(2-F)

46-44
Me
Me
H
Me
H
Me
Ph(2,6-F2)

46-45
Me
Me
H
Me
H
Me
Ph(2-Cl)

46-46
Me
Me
H
Me
H
Me
Ph(2-Me)

46-47
Me
Me
H
Me
H
Me
Ph(2-CF3)

46-48
Me
Me
H
Me
H
Me
Ph(2-F-6-Cl)

[0286]

47

TABLE 47

Physical

Compound

properties

No.
R1
R2
R3
X1
X2
B
(mp ° C.)

47-1
Me
Me
H
H
H
Ph(2-F)

47-2
Me
Me
H
H
H
Ph(2,6-F2)

47-3
Me
Me
H
H
H
Ph(2-Cl)

47-4
Me
Me
H
H
H
Ph(2-Me)

47-5
Me
Me
H
H
H
Ph(2-CF3)

47-6
Me
Me
H
H
H
Ph(2-F-6-Cl)

47-7
Me
Me
H
Cl
H
Ph(2-F)

47-8
Me
Me
H
Cl
H
Ph(2,6-F2)

47-9
Me
Me
H
Cl
H
Ph(2-Cl)

47-10
Me
Me
H
Cl
H
Ph(2-Me)

47-11
Me
Me
H
Cl
H
Ph(2-CF3)

47-12
Me
Me
H
Cl
H
Ph(2-F-6-Cl)

47-13
Me
Me
H
Me
H
Ph(2-F)

47-14
Me
Me
H
Me
H
Ph(2,6-F2)

47-15
Me
Me
H
Me
H
Ph(2-Cl)

47-16
Me
Me
H
Me
H
Ph(2-Me)

47-17
Me
Me
H
Me
H
Ph(2-CF3)

47-18
Me
Me
H
Me
H
Ph(2-F-6-Cl)

47-19
Me
Me
H
H
Cl
Ph(2-F)

47-20
Me
Me
H
H
Cl
Ph(2,6-F2)

47-21
Me
Me
H
H
Cl
Ph(2-Cl)

47-22
Me
Me
H
H
Cl
Ph(2-Me)

47-23
Me
Me
H
H
Cl
Ph(2-CF3)

47-24
Me
Me
H
H
Cl
Ph(2-F-6-Cl)

47-25
Me
Me
H
H
Me
Ph(2-F)

47-26
Me
Me
H
H
Me
Ph(2,6-F2)

47-27
Me
Me
H
H
Me
Ph(2-Cl)

47-28
Me
Me
H
H
Me
Ph(2-Me)

47-29
Me
Me
H
H
Me
Ph(2-CF3)

47-30
Me
Me
H
H
Me
Ph(2-F-6-Cl)

47-31
Me
Me
H
Me
Me
Ph(2-F)

47-32
Me
Me
H
Me
Me
Ph(2,6-F2)

47-33
Me
Me
H
Me
Me
Ph(2-Cl)

47-34
Me
Me
H
Me
Me
Ph(2-Me)

47-35
Me
Me
H
Me
Me
Ph(2-CF3)

47-36
Me
Me
H
Me
Me
Ph(2-F-6-Cl)

[0287]

48

TABLE 48

Physical

Compound

properties

No.
R1
R2
R3
X1
X2
B
(mp ° C.)

48-1
Me
Me
H
H
H
Ph(2-F)

48-2
Me
Me
H
H
H
Ph(2,6-F2)

48-3
Me
Me
H
H
H
Ph(2-Cl)

48-4
Me
Me
H
H
H
Ph(2-Me)

48-5
Me
Me
H
H
H
Ph(2-CF3)

48-6
Me
Me
H
H
H
Ph(2-F-6-Cl)

48-7
Me
Me
H
Cl
H
Ph(2-F)

48-8
Me
Me
H
Cl
H
Ph(2,6-F2)

48-9
Me
Me
H
Cl
H
Ph(2-Cl)

48-10
Me
Me
H
Cl
H
Ph(2-Me)

48-11
Me
Me
H
Cl
H
Ph(2-CF3)

48-12
Me
Me
H
Cl
H
Ph(2-F-6-Cl)

48-13
Me
Me
H
Me
H
Ph(2-F)

48-14
Me
Me
H
Me
H
Ph(2,6-F2)

48-15
Me
Me
H
Me
H
Ph(2-Cl)

48-16
Me
Me
H
Me
H
Ph(2-Me)

48-17
Me
Me
H
Me
H
Ph(2-CF3)

48-18
Me
Me
H
Me
H
Ph(2-F-6-Cl)

48-19
Me
Me
H
H
Cl
Ph(2-F)

48-20
Me
Me
H
H
Cl
Ph(2,6-F2)

48-21
Me
Me
H
H
Cl
Ph(2-Cl)

48-22
Me
Me
H
H
Cl
Ph(2-Me)

48-23
Me
Me
H
H
Cl
Ph(2-CF3)

48-24
Me
Me
H
H
Cl
Ph(2-F-6-Cl)

48-25
Me
Me
H
H
Me
Ph(2-F)

48-26
Me
Me
H
H
Me
Ph(2,6-F2)

48-27
Me
Me
H
H
Me
Ph(2-Cl)

48-28
Me
Me
H
H
Me
Ph(2-Me)

48-29
Me
Me
H
H
Me
Ph(2-CF3)

48-30
Me
Me
H
H
Me
Ph(2-F-6-Cl)

48-31
Me
Me
H
Me
Me
Ph(2-F)

48-32
Me
Me
H
Me
Me
Ph(2,6-F2)

48-33
Me
Me
H
Me
Me
Ph(2-Cl)

48-34
Me
Me
H
Me
Me
Ph(2-Me)

48-35
Me
Me
H
Me
Me
Ph(2-CF3)

48-36
Me
Me
H
Me
Me
Ph(2-F-6-Cl)

[0288]

49

TABLE 49

Physical

Compound

properties

No.
R1
R2
R3
X1
X2
B
(mp ° C.)

49-1
Me
Me
H
H
H
Ph(2-F)

49-2
Me
Me
H
H
H
Ph(2,6-F2)

49-3
Me
Me
H
H
H
Ph(2-Cl)

49-4
Me
Me
H
H
H
Ph(2-Me)

49-5
Me
Me
H
H
H
Ph(2-CF3)

49-6
Me
Me
H
H
H
Ph(2-F-6-Cl)

49-7
Me
Me
H
Cl
H
Ph(2-F)

49-8
Me
Me
H
Cl
H
Ph(2,6-F2)

49-9
Me
Me
H
Cl
H
Ph(2-Cl)

49-10
Me
Me
H
Cl
H
Ph(2-Me)

49-11
Me
Me
H
Cl
H
Ph(2-CF3)

49-12
Me
Me
H
Cl
H
Ph(2-F-6-Cl)

49-13
Me
Me
H
Me
H
Ph(2-F)

49-14
Me
Me
H
Me
H
Ph(2,6-F2)

49-15
Me
Me
H
Me
H
Ph(2-Cl)

49-16
Me
Me
H
Me
H
Ph(2-Me)

49-17
Me
Me
H
Me
H
Ph(2-CF3)

49-18
Me
Me
H
Me
H
Ph(2-F-6-Cl)

49-19
Me
Me
H
H
Ci
Ph(2-F)

49-20
Me
Me
H
H
Cl
Ph(2,6-F2)

49-21
Me
Me
H
H
Cl
Ph(2-Cl)

49-22
Me
Me
H
H
Cl
Ph(2-Me)

49-23
Me
Me
H
H
Cl
Ph(2-CF3)

49-24
Me
Me
H
H
Cl
Ph(2-F-6-Cl)

49-25
Me
Me
H
H
Me
Ph(2-F)

49-26
Me
Me
H
H
Me
Ph(2,6-F2)

49-27
Me
Me
H
H
Me
Ph(2-Cl)

49-28
Me
Me
H
H
Me
Ph(2-Me)

49-29
Me
Me
H
H
Me
Ph(2-CF3)

49-30
Me
Me
H
H
Me
Ph(2-F-6-Cl)

49-31
Me
Me
H
Me
Me
Ph(2-F)

49-32
Me
Me
H
Me
Me
Ph(2,6-F2)

49-33
Me
Me
H
Me
Me
Ph(2-Cl)

49-34
Me
Me
H
Me
Me
Ph(2-Me)

49-35
Me
Me
H
Me
Me
Ph(2-CF3)

49-36
Me
Me
H
Me
Me
Ph(2-F-6-Cl)

[0289]

50

TABLE 50

Physical

Compound

properties

No.
R1
R2
R3
X1
X2
B
(mp ° C.)

50-1
Me
Me
H
H
H
Ph(2-F)

50-2
Me
Me
H
H
H
Ph(2,6-F2)

50-3
Me
Me
H
H
H
Ph(2-Cl)

50-4
Me
Me
H
H
H
Ph(2-Me)

50-5
Me
Me
H
H
H
Ph(2-CF3)

50-6
Me
Me
H
H
H
Ph(2-F-6-Cl)

50-7
Me
Me
H
Cl
H
Ph(2-F)

50-8
Me
Me
H
Cl
H
Ph(2,6-F2)

50-9
Me
Me
H
Cl
H
Ph(2-Cl)

50-10
Me
Me
H
Cl
H
Ph(2-Me)

50-11
Me
Me
H
Cl
H
Ph(2-CF3)

50-12
Me
Me
H
Cl
H
Ph(2-F-6-Cl)

50-13
Me
Me
H
Me
H
Ph(2-F)

50-14
Me
Me
H
Me
H
Ph(2,6-F2)

50-15
Me
Me
H
Me
H
Ph(2-Cl)

50-16
Me
Me
H
Me
H
Ph(2-Me)

50-17
Me
Me
H
Me
H
Ph(2-CF3)

50-18
Me
Me
H
Me
H
Ph(2-F-6-Cl)

50-19
Me
Me
H
H
Cl
Ph(2-F)

50-20
Me
Me
H
H
Cl
Ph(2,6-F2)

50-21
Me
Me
H
H
Cl
Ph(2-Cl)

50-22
Me
Me
H
H
Cl
Ph(2-Me)

50-23
Me
Me
H
H
Cl
Ph(2-CF3)

50-24
Me
Me
H
H
Cl
Ph(2-F-6-Cl)

50-25
Me
Me
H
H
Me
Ph(2-F)

50-26
Me
Me
H
H
Me
Ph(2,6-F2)

50-27
Me
Me
H
H
Me
Ph(2-Cl)

50-28
Me
Me
H
H
Me
Ph(2-Me)

50-29
Me
Me
H
H
Me
Ph(2-CF3)

50-30
Me
Me
H
H
Me
Ph(2-F-6-Cl)

50-31
Me
Me
H
Me
Me
Ph(2-F)

50-32
Me
Me
H
Me
Me
Ph(2,6-F2)

50-33
Me
Me
H
Me
Me
Ph(2-Cl)

50-34
Me
Me
H
Me
Me
Ph(2-Me)

50-35
Me
Me
H
Me
Me
Ph(2-CF3)

50-36
Me
Me
H
Me
Me
Ph(2-F-6-Cl)

[0290]

51

TABLE 51

Physical

Compound

properties

No.
R1
R2
R3
X1
X2
B
(mp ° C.)

51-1
Me
Me
H
H
H
Ph(2-F)
121-122

51-2
Me
Me
H
H
H
Ph(2,6-F2)
147-148

51-3
Me
Me
H
H
H
Ph(2-Cl)

51-4
Me
Me
H
H
H
Ph(2-Me)

51-5
Me
Me
H
H
H
Ph(2-CF3)

51-6
Me
Me
H
H
H
Ph(2-F-6-Cl)

51-7
Me
Me
H
Me
H
Ph(2-F)

51-8
Me
Me
H
Me
H
Ph(2,6-F2)

51-9
Me
Me
H
Me
H
Ph(2-Cl)

51-10
Me
Me
H
Me
H
Ph(2-Me)

51-11
Me
Me
H
Me
H
Ph(2-CF3)

51-12
Me
Me
H
Me
H
Ph(2-F-6-Cl)

51-13
Me
Me
H
Me
Me
Ph(2-F)

51-14
Me
Me
H
Me
Me
Ph(2,6-F2)

51-15
Me
Me
H
Me
Me
Ph(2-Cl)

51-16
Me
Me
H
Me
Me
Ph(2-Me)

51-17
Me
Me
H
Me
Me
Ph(2-CF3)

51-18
Me
Me
H
Me
Me
Ph(2-F-6-Cl)

51-19
Me
Me
H
Me
Cl
Ph(2-F)

51-20
Me
Me
H
Me
Cl
Ph(2,6-F2)

51-21
Me
Me
H
Me
Cl
Ph(2-Cl)

51-22
Me
Me
H
Me
Cl
Ph(2-Me)

51-23
Me
Me
H
Me
Cl
Ph(2-CF3)

51-24
Me
Me
H
Me
Cl
Ph(2-F-6-Cl)

51-25
Me
Me
H
Me
Br
Ph(2-F)

51-26
Me
Me
H
Me
Br
Ph(2,6-F2)

51-27
Me
Me
H
Me
Br
Ph(2-Cl)

51-28
Me
Me
H
Me
Br
Ph(2-Me)

51-29
Me
Me
H
Me
Br
Ph(2-CF3)

51-30
Me
Me
H
Me
Br
Ph(2-F-6-Cl)

51-31
Me
Me
H
Me
CF3
Ph(2-F)

51-32
Me
Me
H
Me
CF3
Ph(2,6-F2)

51-33
Me
Me
H
Me
CF3
Ph(2-Cl)

51-34
Me
Me
H
Me
CF3
Ph(2-Me)

51-35
Me
Me
H
Me
CF3
Ph(2-CF3)

51-36
Me
Me
H
Me
CF3
Ph(2-F-6-Cl)

51-37
Me
Me
H
Me
OCF3
Ph(2-F)

51-38
Me
Me
H
Me
OCF3
Ph(2,6-F2)

51-39
Me
Me
H
Me
OCF3
Ph(2-Cl)

51-40
Me
Me
H
Me
OCF3
Ph(2-Me)

51-41
Me
Me
H
Me
OCF3
Ph(2-CF3)

51-42
Me
Me
H
Me
OCF3
Ph(2-F-6-Cl)

51-43
Me
Me
H
Me
OCHF2
Ph(2-F)

51-44
Me
Me
H
Me
OCHF2
Ph(2,6-F2)

51-45
Me
Me
H
Me
OCHF2
Ph(2-Cl)

51-46
Me
Me
H
Me
OCHF2
Ph(2-Me)

51-47
Me
Me
H
Me
OCHF2
Ph(2-CF3)

51-48
Me
Me
H
Me
OCHF2
Ph(2-F-6-Cl)

51-49
Me
Me
H
Me
OCH2CF3
Ph(2-F)

51-50
Me
Me
H
Me
OCH2CF3
Ph(2,6-F2)

51-51
Me
Me
H
Me
OCH2CF3
Ph(2-Cl)

51-53
Me
Me
H
Me
OCH2CF3
Ph(2-CF3)

51-54
Me
Me
H
Me
OCH2CF3
Ph(2-F-6-Cl)

51-55
Me
Me
H
Cl
H
Ph(2-F)

51-56
Me
Me
H
Cl
H
Ph(2,6-F2)

51-57
Me
Me
H
Cl
H
Ph(2-Cl)

51-58
Me
Me
H
Cl
H
Ph(2-Me)

51-59
Me
Me
H
Cl
H
Ph(2-CF3)

51-60
Me
Me
H
Cl
H
Ph(2-F-6-Cl)

51-61
Me
Me
H
Cl
Me
Ph(2-F)

51-62
Me
Me
H
Cl
Me
Ph(2,6-F2)

51-63
Me
Me
H
Cl
Me
Ph(2-Cl)

51-64
Me
Me
H
Cl
Me
Ph(2-Me)

51-65
Me
Me
H
Cl
Me
Ph(2-CF3)

51-66
Me
Me
H
Cl
Me
Ph(2-F-6-Cl)

51-67
Me
Me
H
Cl
Cl
Ph(2-F)

51-68
Me
Me
H
Cl
Cl
Ph(2,6-F2)

51-69
Me
Me
H
Cl
Cl
Ph(2-Cl)

51-70
Me
Me
H
Cl
Cl
Ph(2-Me)

51-71
Me
Me
H
Cl
Cl
Ph(2-CF3)

51-72
Me
Me
H
Cl
Cl
Ph(2-F-6-Cl)

51-73
Me
Me
H
Cl
Br
Ph(2-F)

51-74
Me
Me
H
Cl
Br
Ph(2,6-F2)

51-75
Me
Me
H
Cl
Br
Ph(2-Cl)

51-76
Me
Me
H
Cl
Br
Ph(2-Me)

51-77
Me
Me
H
Cl
Br
Ph(2-CF3)

51-78
Me
Me
H
Cl
Br
Ph(2-F-6-Cl)

51-79
Me
Me
H
Cl
CF3
Ph(2-F)

51-80
Me
Me
H
Cl
CF3
Ph(2,6-F2)

51-81
Me
Me
H
Cl
CF3
Ph(2-Cl)

51-82
Me
Me
H
Cl
CF3
Ph(2-Me)

51-83
Me
Me
H
Cl
CF3
Ph(2-CF3)

51-84
Me
Me
H
Cl
CF3
Ph(2-F-6-Cl)

51-85
Me
Me
H
Cl
OCF3
Ph(2-F)

51-86
Me
Me
H
Cl
OCF3
Ph(2,6-F2)

51-87
Me
Me
H
Cl
OCF3
Ph(2-Cl)

51-88
Me
Me
H
Cl
OCF3
Ph(2-Me)

51-89
Me
Me
H
Cl
OCF3
Ph(2-CF3)

51-90
Me
Me
H
Cl
OCF3
Ph(2-F-6-Cl)

51-91
Me
Me
H
Cl
OCHF2
Ph(2-F)

51-92
Me
Me
H
Cl
OCHF2
Ph(2,6-F2)

51-93
Me
Me
H
Cl
OCHF2
Ph(2-Cl)

51-94
Me
Me
H
Cl
OCHF2
Ph(2-Me)

51-95
Me
Me
H
Cl
OCHF2
Ph(2-CF3)

51-96
Me
Me
H
Cl
OCHF2
Ph(2-F-6-Cl)

51-97
Me
Me
H
Cl
OCH2CF3
Ph(2-F)

51-98
Me
Me
H
Cl
OCH2CF3
Ph(2,6-F2)

51-99
Me
Me
H
Cl
OCH2CF3
Ph(2-Cl)

51-100
Me
Me
H
Cl
OCH2CF3
Ph(2-Me)

51-101
Me
Me
H
Cl
OCH2CF3
Ph(2-CF3)

51-102
Me
Me
H
Cl
OCH2CF3
Ph(2-F-6-Cl)

[0291]

52

TABLE 2

Physical

Compound

properties

No.
R1
R2
R3
X1
X2
X3
B
(mp ° C.)

52-1
Me
Me
H
H
H
H
Ph(2-F)

52-2
Me
Me
H
H
H
H
Ph(2,6-F2)

52-3
Me
Me
H
H
H
H
Ph(2-Cl)

52-4
Me
Me
H
H
H
H
Ph(2-Me)

52-5
Me
Me
H
H
H
H
Ph(2-CF3)

52-6
Me
Me
H
H
H
H
Ph(2-F-6-Cl)

52-7
Me
Me
H
H
Me
H
Ph(2-F)

52-8
Me
Me
H
H
Me
H
Ph(2,6-F2)

52-9
Me
Me
H
H
Me
H
Ph(2-Cl)

52-10
Me
Me
H
H
Me
H
Ph(2-Me)

52-11
Me
Me
H
H
Me
H
Ph(2-CF3)

52-12
Me
Me
H
H
Me
H
Ph(2-F-6-Cl)

52-13
Me
Me
H
H
H
Me
Ph(2-F)

52-14
Me
Me
H
H
H
Me
Ph(2,6-F2)

52-15
Me
Me
H
H
H
Me
Ph(2-Cl)

52-16
Me
Me
H
H
H
Me
Ph(2-Me)

52-17
Me
Me
H
H
H
Me
Ph(2-CF3)

52-18
Me
Me
H
H
H
Me
Ph(2-F-6-Cl)

52-19
Me
Me
H
F
H
H
Ph(2-F)

52-20
Me
Me
H
F
H
H
Ph(2,6-F2)

52-21
Me
Me
H
F
H
H
Ph(2-Cl)

52-22
Me
Me
H
F
H
H
Ph(2-Me)

52-23
Me
Me
H
F
H
H
Ph(2-CF3)

52-24
Me
Me
H
F
H
H
Ph(2-F-6-Cl)

52-25
Me
Me
H
F
Me
H
Ph(2-F)

52-26
Me
Me
H
F
Me
H
Ph(2,6-F2)

52-27
Me
Me
H
F
Me
H
Ph(2-Cl)

52-28
Me
Me
H
F
Me
H
Ph(2-Me)

52-29
Me
Me
H
F
Me
H
Ph(2-CF3)

52-30
Me
Me
H
F
Me
H
Ph(2-F-6-Cl)

52-31
Me
Me
H
F
Cl
H
Ph(2-F)

52-32
Me
Me
H
F
Cl
H
Ph(2,6-F2)

52-33
Me
Me
H
F
Cl
H
Ph(2-Cl)

52-34
Me
Me
H
F
Cl
H
Ph(2-Me)

52-35
Me
Me
H
F
Cl
H
Ph(2-CF3)

52-36
Me
Me
H
F
Cl
H
Ph(2-F-6-Cl)

52-37
Me
Me
H
F
H
Me
Ph(2-F)

52-38
Me
Me
H
F
H
Me
Ph(2,6-F2)

52-39
Me
Me
H
F
H
Me
Ph(2-Cl)

52-40
Me
Me
H
F
H
Me
Ph(2-Me)

52-41
Me
Me
H
F
H
Me
Ph(2-CF3)

52-42
Me
Me
H
F
H
Me
Ph(2-F-6-Cl)

52-43
Me
Me
H
H
Cl
H
Ph(2-F)

52-44
Me
Me
H
H
Cl
H
Ph(2,6-F2)

52-45
Me
Me
H
H
Cl
H
Ph(2-Cl)

52-46
Me
Me
H
H
Cl
H
Ph(2-Me)

52-47
Me
Me
H
H
Cl
H
Ph(2-CF3)

52-48
Me
Me
H
H
Cl
H
Ph(2-F-6-Cl)

52-49
Me
Me
H
H
H
Cl
Ph(2-F)

52-50
Me
Me
H
H
H
Cl
Ph(2,6-F2)

52-51
Me
Me
H
H
H
Cl
Ph(2-Cl)

52-52
Me
Me
H
H
H
Cl
Ph(2-Me)

52-53
Me
Me
H
H
H
Cl
Ph(2-CF3)

52-54
Me
Me
H
H
H
Cl
Ph(2-F-6-Cl)

52-55
Me
Me
H
F
H
Cl
Ph(2-F)

52-56
Me
Me
H
F
H
Cl
Ph(2,6-F2)

52-57
Me
Me
H
F
H
Cl
Ph(2-Cl)

52-58
Me
Me
H
F
H
Cl
Ph(2-Me)

52-59
Me
Me
H
F
H
Cl
Ph(2-CF3)

52-60
Me
Me
H
F
H
Cl
Ph(2-F-6-Cl)

[0292]

53

TABLE 53

Physical

Compound

properties

No.
R1
R2
R3
X1
X2
B
(mp ° C.)

53-1
Me
Me
H
H
H
Ph(2-F)

53-2
Me
Me
H
H
H
Ph(2,6-F2)

53-3
Me
Me
H
H
H
Ph(2-Cl)

53-4
Me
Me
H
H
H
Ph(2-Me)

53-5
Me
Me
H
H
H
Ph(2-CF3)

53-6
Me
Me
H
H
H
Ph(2-F-6-Cl)

53-7
Me
Me
H
Cl
H
Ph(2-F)

53-8
Me
Me
H
Cl
H
Ph(2,6-F2)

53-9
Me
Me
H
Cl
H
Ph(2-Cl)

53-10
Me
Me
H
Cl
H
Ph(2-Me)

53-11
Me
Me
H
Cl
H
Ph(2-CF3)

53-12
Me
Me
H
Cl
H
Ph(2-F-6-Cl)

53-13
Me
Me
H
Me
H
Ph(2-F)

53-14
Me
Me
H
Me
H
Ph(2,6-F2)

53-15
Me
Me
H
Me
H
Ph(2-Cl)

53-16
Me
Me
H
Me
H
Ph(2-Me)

53-17
Me
Me
H
Me
H
Ph(2-CF3)

53-18
Me
Me
H
Me
H
Ph(2-F-6-Cl)

53-19
Me
Me
H
H
Cl
Ph(2-F)

53-20
Me
Me
H
H
Cl
Ph(2,6-F2)

53-21
Me
Me
H
H
Cl
Ph(2-Cl)

53-22
Me
Me
H
H
Cl
Ph(2-Me)

53-23
Me
Me
H
H
Cl
Ph(2-CF3)

53-24
Me
Me
H
H
Cl
Ph(2-F-6-Cl)

53-25
Me
Me
H
H
Me
Ph(2-F)

53-26
Me
Me
H
H
Me
Ph(2,6-F2)

53-27
Me
Me
H
H
Me
Ph(2-Cl)

53-28
Me
Me
H
H
Me
Ph(2-Me)

53-29
Me
Me
H
H
Me
Ph(2-CF3)

53-30
Me
Me
H
H
Me
Ph(2-F-6-Cl)

53-31
Me
Me
H
Me
Me
Ph(2-F)

53-32
Me
Me
H
Me
Me
Ph(2,6-F2)

53-33
Me
Me
H
Me
Me
Ph(2-Cl)

53-34
Me
Me
H
Me
Me
Ph(2-Me)

53-35
Me
Me
H
Me
Me
Ph(2-CF3)

53-36
Me
Me
H
Me
Me
Ph(2-F-6-Cl)

[0293] Now, Test Examples will be described.

TEST EXAMPLE 1

[0294] Test on Southern Root-knot Nematode (Meloidgyne incognita) (Soil incorporation)

[0295] To 300 ml of the soil contaminated by southern root-knot nematode, 7 ml of a chemical solution having the concentration of the compound of the present invention adjusted to be 1600 ppm, is poured, followed by mixing so that the compound is uniformly dispersed. The treated soil is put into a pot (diameter: 9 cm, height: 8 cm), and then a tomato seedling in 2-leaf stage is transplanted and placed in a greenhouse. After three to four weeks from the transplantation of the tomato, the root knot index is determined based on the following standards. The compound of the present invention shows high controlling effects at a level of a root knot index of not more than 1. For example, the compound Nos. 1-25, 1-26, 1-73, 1-100, 1-122, 1-123, 1-125, 1-127, 1-130, 1-131, 1-133, 1-136, 1-137, 1-139, 1-140, 1-172, 1-173, 1-177, 5-5, 5-9, 5-11, 5-16, 5-20, 8-2, 8-5, 13-2, 13-4, 13-6, 13-7, 13-18, 13-19, 13-44, 13-45, 16-32, 16-37 and 16-38 were at a level of a root knot index of not more than 1.

54Degree of formation of rootRoot knot indexknots0No knot was formed1Knots were formed to aslight degree2Knots were formed to amoderate degree3Knots were formed to a heavydegree4Knots were formed to theheaviest degree

TEST EXAMPLE 2

[0296] Test on Cobb Root-lesion Nematode (Pratylenchus penetrans) (Soil incorporation)

[0297] To 300 ml of the soil contaminated by Cobb root-lesion nematode, 7 ml of a chemical solution having the concentration of the compound of the present invention adjusted to be 1600 ppm, is poured, followed by mixing so that the compound is uniformly dispersed. The treated soil is put into a pot (diameter: 9 cm, height: 8 cm), and then 10 seeds of burdock are disseminated and placed in a greenhouse. After about two months from the dissemination of the burdock seeds, injury level of the roots is determined based on the following standards. The compound of the present invention shows high controlling effects at a level of an injury index of not more than 1. For example, the compound Nos. 13-19 and 13-45 were at a level of an injury index of not more than 1.

55Injury indexInjury level of roots0No injury1Slight injury2Moderate injury3Heavy injury4Heaviest injury

TEST EXAMPLE 3

[0298] Test on Cobb Root-lesion Nematode (Immersion Treatment)

[0299] To a test tube made of glass (DISPOSABLE CULTURE TUBE manufactured by IWAKI Co., Ltd: internal diameter: 10 mm, lengh: 75 mm), 1 ml of a chemical solution having the concentration of the compound of the present invention adjusted to be 40 ppm, is poured. 1 ml of water having about 100 of Cobb root-lesion nematodes is added thereto, followed by stirring gently. The final concentration of the compound of the present invention in the obtained solution is 20 ppm. Then, the top of the test tube is covered with a Para film (Manufactured by American National Can Co., Ltd) to obdurate, and then it is left at 25° C. After two days, the above solution is transferred to a slide glass (MICRO SLIDE GLASS manufactured by MATSUNAMI Co., Ltd: With plankton lattice lines), the number of inactive nematodes (including ones which do not move at least 10 seconds) and the number of active nematodes are counted by a microscope. The motility inhibition ratio (%) is calculated based on the following formula. As a result, the compound of the present invention shows high controlling effects at a level of a motility inhibition ratio (%) of not less than 70%. For example, the motility inhibition ratio of the compounds Nos. 13-45, 16-37 and 16-38 showed at a level of a motility inhibition ratio of not less than 70%.

[0300] Motility inhibition ratio (%)=The number of inactive nematodes/(The number of active nematodes+The number of inactive nematodes)×100

TEST EXAMPLE 4

[0301] Test on Coccidia

[0302]

Eimeria tenella
of wild type is infected to chicks to obtain fresh immature oocysts, which are then exposed to a solution having a predetermined concentration of the compound of the present invention for 10 or 30 minutes. The exposed immature oocysts are subjected to centrifugal separation, and after removing the supernatant, a 2% potassium bichromate aqueous solution is added, followed by sporulation at 25° C. for 4 days, whereby good oosyst controlling effects are confirmed.

TEST EXAMPLE 5

[0303] Test on Gog Filarioidea

[0304] To a dog subcutaneously infected with dog filarioidea (Dirofilaria immitis), the compound of the present invention is orally administered. At the time of an autopsy after 200 days from the infection, the number of adults of dog filarioidea parasitic to the lung or heart of the treated animal is investigated, whereby good effects for controlling dog filarioidea is confirmed.

[0305] Now, formulation Examples will be described.

56FORMULATION EXAMPLE 1(1) Compound of the present invention20 parts by weight(2) Clay72 parts by weight(3) Sodium lignin sulfonate 8 parts by weight

[0306] The above components are uniformly mixed to obtain a wettable powder.

57FORMULATION EXAMPLE 2(1) Compound of the present invention 5 parts by weight(2) Talc95 parts by weight

[0307] The above components are uniformly mixed to obtain a dust.

58FORMULATION EXAMPLE 3(1) Compound of the present invention20 parts by weight(2) N,N′-dimethylacetamide20 parts by weight(3) Polyoxyethylenealkylphenyl ether10 parts by weight(4) Xylene50 parts by weight

[0308] The above components are uniformly mixed and dissolved to obtain an emulsifiable concentrate.

59FORMULATION EXAMPLE 4(1) Clay68 parts by weight(2) Sodium lignin sulfonate 2 parts by weight(3) Polyoxyethylenealkylaryl sulfate 5 parts by weight(4) Fine silica powder25 parts by weight

[0309] A mixture of the above components is mixed with compound of the present invention in a weight ratio of 4:1 to obtain a wettable powder.

60FORMULATION EXAMPLE 5(1) Compound of the present invention 50 parts by weight(2) Oxylated polyalkylphenyl 2 parts by weight phosphate-triethanolamine(3) Silicone 0.2 part by weight(4) Water47.8 parts by weightThe above components are uniformly mixed and pulverized to obtain abase liquid, and(5) Sodium polycarboxylate 5 parts by weight(6) Anhydrous sodium sulfate42.8 parts by weightare added, and the mixture is uniformly mixed and driedto obtain water-dispersible granules.

[0310]

61

FORMULATION EXAMPLE 6

(1) Compound of the present invention
5 parts by weight

(2) Polyoxyethyleneoctylphenyl ether
1 part by weight

(3) polyoxyethylene phosphoric acid ester
0.1 part by weight

(4) Granular calcium carbonate
93.9 parts by weight

[0311] The above components (1) to (3) are preliminarily uniformly mixed and diluted with a proper amount of acetone, and then the mixture is sprayed onto the component (4), and acetone is removed to obtain granules.

62FORMULATION EXAMPLE 7(1) Compound of the present invention 2.5 parts by weight(2) N-methyl-2-pyrrolidone 2.5 parts by weight(3) Soybean oil95.0 parts by weight

[0312] The above components are uniformly mixed and dissolved to obtain an ultra low volume formulation.

Acid amide derivatives, process for producing these, and pest agent containing these

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