Anthranilic acid derivative

Abstract

The present invention relates to an anthranilic acid derivative expressed by the following formula (1) or the following formula (2), or its pharmacologically permissible salt or solvate. 1

Description

TECHNICAL FIELD

[0001] The present invention relates to a new anthranilic acid derivative expressed by the formula (1) or the formula (2), its pharmacologically permissible salts or solvated products (which may be collectively called as “the anthranilic acid derivative of the present invention” hereinafter), a pharmaceutical composition composed thereof and a preventive and/or therapeutic agent composed thereof. More particularly, it relates to a new anthranilic acid derivative having benzene skeleton or pyridine skeleton on the principal anthranilic acid skeleton and further having a benzene skeleton or a naphthalene skeleton substituted by a side chain containing hetero-atom, i.e. a derivative having three aromatic groups at the same time, its pharmacologically permissible salt or solvated product, a pharmaceutical composition composed thereof and a preventive and/or therapeutic agent composed thereof.

[0002] Further, the anthranilic acid derivative of the present invention is a compound clinically applicable as a carcinostatic agent owing to its strong cytotoxic action and also clinically applicable as a preventive and/or therapeutic agent for allergic diseases owing to its activity to suppress the formation of IgE antibody.

BACKGROUND ARTS

[0003] Examples of the compound having naphthalene skeleton and anthranilic acid skeleton at the same time are those disclosed in the specification of JP-A 1-287066 (hereinunder, JP-A means “Japanese Unexamined Patent Application”). The specification describes compounds such as N-(2-naphthoyl)anthranylbenzoic acid and shows that these compounds have antiallergic activity or 5-lipoxygenase inhibiting activity. However, these compounds consist of a bicyclic aromatic ring derivative substituted by hydroxyl group or alkoxy group and directly bonded to an anthranilic acid skeleton through an amide bond, and there is no description or suggestion in the specification whether these compounds have cytotoxic action or IgE antibody production suppressing action or not.

[0004] Compounds having naphthalene skeleton and anthranilic acid skeleton and exhibiting antiallergic activity and IgE antibody production suppressing activity are described in the specifications of JP-A 1-106818, International Application WO90/12001 and JP-A 7-285858. However, these compounds are different from the compound of the present invention because there is no compound having a principal skeleton containing three aromatic rings at the same time in these compounds.

[0005] International Application WO95/32943 and a document “Journal of Medicinal Chemistry (J. Med. Chem.) vol.40, No.4, sections 395-407 (1997)” describe compounds having naphthalene skeleton and anthranilic acid skeleton and exhibiting antiallergic activity and IgE antibody production suppressing activity. Further, International Application WO97/19910 describes compounds having benzene skeleton and anthranilic acid skeleton and exhibiting antiallergic activity and IgE antibody production suppressing activity. However, these compounds are also different from the compound of the present invention because the substituent corresponding to the side chain of benzene skeleton or naphthalene skeleton is limited to alkoxy groups, alkenyloxy groups or aralkyloxy groups. Furthermore, the specification merely describes the presence of antiallergic activity and IgE antibody production suppressing activity in these compounds having the above specific substituents.

[0006] Compounds having pyridine ring skeleton and anthranilic acid skeleton and exhibiting antibacterial activity are described in the specification of International Application WO95/25723. The specification further describes that the substituent of the pyridine ring includes phenyloxy group and phenylthio group which may have substituents. However, there is no detailed explanation on the kind of the substituents. In the compounds of the present invention, for example, the pyridine ring is always substituted by phenyloxy group, phenylthio group, phenylsulfonyl group, phenylsulfinyl group, phenylcarbonyl group, phenylmethyl group, naphthyloxy group, naphthylthio group, naphthylsulfonyl group, naphthylsuifinyl group, naphthylcarbonyl group or naphthylmethyl group and furthermore the phenyl group or the naphthyl group constitutes the mother nucleus and always substituted by alkoxy group, aryloxy group, etc., which may contain hetero-atoms and, accordingly, the compound of the present invention is different from the compounds described in the above specification. Further, there is no comment on the IgE antibody production suppressing activity in the specification.

[0007] Meanwhile, the creation of a new compound having strong cytotoxic action is extremely important in the development of an excellent carcinostatic agent. Since the carcinostatic activity and carcinostatic spectrum of a compound are highly dependent upon its chemical structure in general, it is highly possible to enable the development of a carcinostatic agent having excellent characteristics compared with conventional carcinostatic agents practically in use at present from a cytotoxic compound having a new structure different from the structure of known compounds.

[0008] Examples of known low-molecular compound having benzene skeleton or aryl skeleton and exhibiting cytotoxic activity are substituted phenylsulfonyl derivative (JP-A 5-9170), 2-arylquinolinol derivative (JP-A 7-33743) and benzoylacetylene derivative (JP-A 7-97350).

[0009] However, the fact that a compound having benzene skeleton or aryl skeleton together with anthranilic acid skeleton has cytotoxic activity or carcinostatic activity is utterly unknown.

[0010] The object of the present invention is to provide a new compound usable as a clinically applicable therapeutic agent for cancer and preventive and/or therapeutic agent for allergic diseases.

DISCLOSURE OF THE INVENTION

[0011] As a result of vigorous investigation performed by the inventors of the present invention to achieve the above purpose, the inventors have found the following items 1 to 16 and completed the present invention.

[0012] In the description of atomic group expressing substituent, etc., the mark “-” showing the direction of bond is described in a group supposed to have ambiguous bonding form, however, the mark may be omitted for a group having clear bonding form.

[0013] 1. The anthranilic acid derivative expressed by the following formula (1) or the following formula (2) or its pharmacologically permissible salt or solvate. 2

[0014] <<in the formulas, Y1 is the group of the following formula (3)-1 or (3)-2. 3

[0015] {in the formulas, Z is a straight-chain, branched or cyclic saturated, unsaturated or aromatic C1 to C12 hydrocarbon group substituted by one or more —NR10R11, —COOR12, —(C═O)NR13R14, —(C═O)R15 or OR16 [the C1 to C12 hydrocarbon group is optionally substituted by a substituent L (L is a C1 to C6 alkyl group, a halogen atom, —NO2 or —CN)],

[0016] a 3 to 8-membered saturated ring containing one or plural —NR17—, —O— or —S— in the ring and optionally containing one or more —C(═O)— groups in the ring, a C1 to C4 straight or branched-chain saturated or unsaturated hydrocarbon group having one or two double bonds or triple bonds and optionally substituted by the above 3 to 8-membered ring, or a C5 to C10 straight or branched-chain saturated or unsaturated hydrocarbon group substituted by a monocyclic or bicyclic aromatic ring containing one or more hetero-atoms selected from oxygen, nitrogen and sulfur atom in the ring (the aromatic ring is optionally substituted by the substituent L).

[0017] the groups R10, R11, R12, R13, R14, R15, R16, and R17 are each independently hydrogen atom, a straight or branched-chain C1 to C6 alkyl group which is optionally substituted, a C7 to C11 aralkyl group which is optionally substituted, a C6 to C10 aryl group which is optionally substituted (the substituent is a halogen atom, —OH, a C1 to C4 alkoxy group, —CN, —NO2 or —COOR18), or a group selected from the following formulas (4)-1, (4)-2 and (4)-3. The groups R10 and R11, or R13 and R14 may together form a 3 to 12-membered ring optionally containing one or more —O—, —S—, —NR18— or —(C═O)— groups. 4

[0018] [in the formulas, Q is a C1 to C10 alkyl group which is optionally substituted, a C2 to C6 alkenyl group which is optionally substituted, a C1 to C6 alkoxy group which is optionally substituted, a C7 to C11 aralkyl group which is optionally substituted, a C7 to C11 aralkyloxy group which is optionally substituted (the substituent is a halogen atom, —OH, —CN, —NO2, —COOR19 or phenoxy group), dimethylamino group, morpholino group or a monocyclic or bicyclic aromatic hydrocarbon group which may have one or more hetero-atoms selected from oxygen, nitrogen and sulfur atoms. [when a monocyclic or bicyclic aromatic hydrocarbon group which may have one or more hetero-atoms is selected in the above case, the ring is optionally substituted at arbitrary positions independently by one or plural substituents selected from halogen atom, —OH, —NO2, —CN, —COOR19, —NR19R20, straight or branched-chain C1 to C6 alkyl group, straight or branched-chain C1 to C6 alkoxy group (in this case, the substituents at adjacent positions may form an acetal bond), straight or branched-chain C1 to C6 alkylthio group, straight or branched-chain C1 to C6 alkylsulfonyl group, straight or branched-chain C1 to C6 acyl group, straight or branched-chain C1 to C6 acylamino group, trihalomethyl group, trihalomethoxy group, phenyl group, or phenoxy group which is optionally substituted by one or more halogen atoms],

[0019] the groups R19 and R20 are each independently hydrogen atom or a C1 to C4 alkyl group],

[0020] the group R18 is hydrogen atom or a C1 to C4 alkyl group,

[0021] the group X3 is —(C═O)—, —O—, —S—, —(S═O)—, SO2, —NR21—, *—NR21(C═O) or *—(C═O)NR21 (the sign (*—) representing a bond means the bonding to the benzene ring or the naphthalene ring in the formula (3)-1 or the formula (3)-2),

[0022] the group R21 is hydrogen atom or a C1 to C4 hydrocarbon group which is optionally substituted by a halogen,

[0023] the groups R5 and R6 are each independently hydrogen atom, a halogen atom, —NO2, —CO2H, —CN, —OR22, —NH(C═O)R22, —(C═O)NHR22 or a C1 to C4 straight or branched-chain saturated or unsaturated hydrocarbon group which is optionally substituted by halogen atom,

[0024] the group R22 is a C1 to C3 hydrocarbon group which is optionally substituted by hydrogen atom or halogen atom},

[0025] the group Y2 is the formula (3)-1, the formula (3)-2, the following formula (5)-1 or the following formula (5)-2, 5

[0026] <in the formulas, the group R7 is hydrogen atom or a substituted or unsubstituted straight-chain, branched or alicyclic saturated or unsaturated C1 to C12 hydrocarbon group having one or two double bonds or triple bonds [in this case, the substituent is a halogen atom, —NO2, —CN, a substituted or unsubstituted phenyl group (in this case, the substituent is a halogen atom, —NO2, —CN, —CF3 or a C1 to C4 hydrocarbon group), or a substituted or unsubstituted 5 to 8-membered cycloalkyl group (in this case, the substituent is a halogen atom or a C1 to C4 hydrocarbon group)],

[0027] the group X4 is —(C═O)—, —O—, —S—, —(S═O)—, —(O═S═O)—, —NR23—, *—NR23CO or *—CONR23 (the group R23 is hydrogen atom or a C1 to C4 hydrocarbon group which is optionally substituted by halogen atom. In this case, the sign (*—) means the bonding to the benzene ring or the naphthalene ring of the formula (5)-1 or the formula (5)-2. The group R7 is not hydrogen atom when the group X4 is —(C═O)—, —(S═O)—, —(O═S═O)— or *—NR23(C═O)—,

[0028] the groups R8 and R9 are each independently hydrogen atom, a halogen atom, —NO2, —CO2H, —CN, —OR24, —NH(C═O)R24, —(C═O)NHR24 or a straight or branched-chain saturated or unsaturated C1 to C4 hydrocarbon group which is optionally substituted by halogen atom (the group R24 is hydrogen atom or a C1 to C3 hydrocarbon group which is optionally substituted by halogen atom)),

[0029] the group X1 is —(C═O)—, —O—, —S—, —(S═O)—, —(O═S═O)— or —CH2—,

[0030] the group X2 is O or S,

[0031] the groups R1 and R2 are each independently hydrogen atom, a halogen atom, —NO2, —CO2H, —CN, —OR25, —NH(C═O)R25, —(C═O)NHR25 or a C1 to C4 straight or branched-chain saturated or unsaturated hydrocarbon group which is optionally substituted by halogen atom,

[0032] the group R25 is hydrogen atom or a C1 to C3 hydrocarbon group which is optionally substituted by halogen atom,

[0033] the groups R3 and R4 are each independently hydrogen atom or a C1 to C4 hydrocarbon group,

[0034] the group A is N, N→O or N+—CH3, and

[0035] n is an integer of 0 to 3.>>.

[0036] 2. The above anthranilic acid derivative wherein Y2 is the group of the formula (3)-1 or the formula (3)-2 or its pharmacologically permissible salt or solvate.

[0037] 3. An anthranilic acid derivative expressed solely by the formula (1), or its pharmacologically permissible salt or solvate.

[0038] 4. An anthranilic acid derivative expressed solely by the formula (2) wherein the group Y2 is expressed by the formula (3)-1 or the formula (3)-2, or its pharmacologically permissible salt or solvate.

[0039] 5. An anthranilic acid derivative expressed solely by the formula (2) wherein the group Y2 is expressed by the formula (5)-1 or the formula (5)2, or its pharmacologically permissible salt or solvate.

[0040] 6. An anthranilic acid derivative of the formula (1) wherein the group Y1 is expressed by the following formula (9)-1, (9)-2 or (9)-3, or its pharmacologically permissible salt or solvate. 6

[0041] <in the formula, the definitions of Z, X3, R5 and R6 are same as those of the formula (3)-1 or the formula (3)-2>

[0042] 7. An anthranilic acid derivative of the formula (2) wherein the group Y2 is expressed by the formula (5)-1, the formula (5)-2, the formula (9)-1, the formula (9)-2 or the formula (9)-3, or its pharmacologically permissible salt or solvate.

[0043] 8. The anthranilic acid derivative of the formula (1) or the formula (2) wherein the group Z is a straight-chain, branched or cyclic saturated, unsaturated or aromatic C1 to C12 hydrocarbon group substituted by one or more —NR10R11, —COOR12, —(C═O)NR13R14, —(C═O)R15 or —OR16 [the C1 to C12 hydrocarbon group is optionally further substituted by substituent L (L is a C1 to C6 alkyl group, halogen atom, —NO2 or —CN)], or its pharmacologically permissible salt or solvate.

[0044] 9. An anthranilic acid derivative of the formula (1) or the formula (2) wherein the group Z is a saturated 3 to 8-membered ring containing one or plural —NR17—, —O— or —S— groups and optionally containing one or more groups in the ring, or a C1 to C4 straight or branched-chain saturated or unsaturated hydrocarbon group having one or two double bonds or triple bonds and optionally substituted by the above 3 to 8-membered ring, or its pharmacologically permissible salt or solvate.

[0045] 10. The anthranilic acid derivative of the formula (1) or the formula (2) wherein the group Z is a C5 to C10 straight or branched-chain saturated or unsaturated hydrocarbon group substituted by a monocyclic or bicyclic aromatic ring containing one or more hetero-atoms selected from oxygen, nitrogen and sulfur atom in the ring (the aromatic ring is optionally substituted by a substituent L), or its pharmacologically permissible salt or solvate.

[0046] 11. A pharmaceutical composition composed of the above anthranilic acid derivative or its pharmacologically permissible salt or solvate, and a pharmacologically permissible carrier.

[0047] 12. The above pharmaceutical composition having cytotoxic activity.

[0048] 13. A therapeutic agent for cancer composed of the above pharmaceutical composition.

[0049] 14. The above pharmaceutical composition having IgE antibody production suppressing action.

[0050] 15. A preventive or therapeutic agent for allergic diseases composed of the above pharmaceutical composition.

[0051] 16. The above preventive or therapeutic agent wherein said allergic diseases are bronchial asthma, allergic rhinitis, allergic conjunctivitis, atopic dermatitis, anaphylactic shock, mite allergy, pollinosis, food allergy, urticaria, ulcerative colitis, eosinophilic gastroenteritis or drug-induced rash.

BEST MODE FOR CARRYING OUT THE INVENTION

[0052] The present invention is described in more detail as follows.

[0053] In the formula (1) expressing the anthranilic acid derivative of the present invention, Y1 is a group selected from the formula (3)-1 and the formula (3)-2. 7

[0054] In the formulas, ZX3, R5 and R6 are substituted one for each to the benzene ring or the naphthalene ring, however, the group ZX3— is preferably positioned at a site expressed in the following formulas (9)-1 to (9)-3. 8

[0055] R5 and R6 are each independently hydrogen atom, a halogen atom, —NO2, —CO2H, —CN, —OR22, —NH(C═O)R22 or —(C═O)NHR22 or a C1-C4 straight or branched-chain saturated or unsaturated hydrocarbon group which may be substituted by halogen atom, and preferably hydrogen atom, a halogen atom, —NO2, —CN, —OH, —OCH3, —NH(C═O)CH3, —(C═O)NHCH3 or a C1-C4 straight or branched-chain saturated or unsaturated hydrocarbon group which may be substituted by halogen atom. More preferably, it is hydrogen atom, a halogen atom, —CH3, —OH or —OCH3 and, especially, hydrogen atom.

[0056] In the formula (3)-1 or the formula (3)-2, Z is a C1-C12 (the carbon number is restricted to those allowable from its structure) straight, branched or cyclic saturated or unsaturated hydrocarbon group or aromatic hydrocarbon group substituted by one or more substituents selected from —NR10R11, —COOR12, —(C═O)NR13R14, —(C═O)R15 and —OR16 and optionally substituted by a substituent L, or a saturated 3 to 8-membered ring having one or plural NR17, O or S in the ring and optionally containing one or more —C(═O)— groups in the ring or a C5-C10 straight or branched-chain saturated or unsaturated hydrocarbon group substituted by a C1-C4 straight or branched-chain or unsaturated hydrocarbon group having one or two double bonds or triple bonds and optionally substituted by the above 3 to 8-membered ring or by a monocyclic or bicyclic aromatic ring (which may be substituted by the substituent L) containing one or more hetero-atoms selected from oxygen, nitrogen and sulfur. The carbon number of the C1-C12 hydrocarbon group of Z is the number of carbon atoms of the main chain and the carbon numbers of the substituents are not included in the carbon number.

[0057] When the group Z is a C1-C12 straight, branched or cyclic saturated or unsaturated hydrocarbon or an aromatic hydrocarbon, it is for example methyl group, ethyl group, propyl group, butyl group, isobutyl group, hexyl group, 2-ethylpropyl group, 1,1-dimethylethyl group, allyl group, methallyl group, cyclohexyl group, cyclooctyl group, cyclopentylmethyl group, cyclohexenylmethyl group, 1-decalyl group, phenyl group, benzyl group and phenylpropyl group, and especially preferably methyl group, ethyl group, cyclohexyl group, cydopentylmethyl group, benzyl group or phenylpropyl group. These hydrocarbon groups are substituted by one or more —NR10R11, —COOR12, —(C═O)NR13R14, —(C═O)R15 or —OR16 groups.

[0058] In the definitions of the formula (3)-1 and the formula (3)-2, the group Z is a saturated 3 to 8-membered ring containing one or plural —NR17—, —O— or —S— groups in the ring and optionally containing one or more —C(═O)— groups, or a C1-C4 straight or branched-chain saturated hydrocarbon group or unsaturated hydrocarbon group containing one or two double bonds or triple bonds wherein these hydrocarbon groups may be substituted by the above 3 to 8-membered ring.

[0059] When Z is a C1-C4 straight or branched-chain saturated hydrocarbon group or unsaturated hydrocarbon group containing one or two double bonds or triple bonds wherein these hydrocarbon groups may be substituted by a saturated 3 to 8-membered ring containing one or plural —NR17—, —O— or —S— groups in the ring and optionally containing one or more —C(═O)— groups, the number of carbon atoms of the C1-C4 hydrocarbon does not include the carbon number of the ring. The substitution position of the main chain on the ring is an arbitrary carbon atom constituting the ring. In the above sentence, the main chain means a C1-C4 straight or branched-chain saturated hydrocarbon group or unsaturated hydrocarbon group containing one or two double bonds or triple bonds.

[0060] When the group Z is a saturated 3 to 8-membered ring containing one or plural —NR17—, —O— or —S— groups in the ring and optionally containing one or more —C(═O)— groups, the substitution position of the group Xs defined in the formula (3)-1 and the formula (3)-2 is an arbitrary carbon atom constituting the ring.

[0061] The saturated 3 to 8-membered ring containing one or plural —NR17—, —O— or —S— groups in the ring and optionally containing one or more —C(═O)— groups is, for example, pyrrolidine ring, piperidine ring, pyrrolidone ring, piperazine ring, morpholine ring, thiomorpholine ring, tetrahydropyran ring and tetrahydrothiophene ring and especially preferably pyrrolidine ring, piperidine ring and piperazine ring.

[0062] In the C1-C4 straight or branched-chain saturated hydrocarbon group or unsaturated hydrocarbon group having one or two double bonds or triple bonds and substituted by a 3 to 8-membered ring, the straight-chain group is e.g. methyl group, ethyl group, n-propyl group, n-butyl group, 2-propenyl group, 3-butenyl group and 2-propynyl group, preferably methyl group, ethyl group, n-propyl group or n-butyl group, especially preferably methyl group or ethyl group.

[0063] The branched-chain group is e.g. isopropyl group, t-butyl group and 2-methylpropyl group and, among the above examples, isopropyl group and t-butyl group are preferable. In the definition in the formula (3)-1 and the formula (3)-2, the group Z is a C5-C10 straight or branched-chain saturated or unsaturated hydrocarbon group substituted by monocyclic or bicyclic aromatic ring (the aromatic ring may be substituted by a substituent L) containing one or more hetero-atoms selected from oxygen, nitrogen and sulfur atom in the ring.

[0064] The term “C5-C10” means the total number of carbon atoms including the carbon atoms of substituents.

[0065] The monocyclic or bicyclic aromatic ring containing one or more hetero-atoms selected from oxygen, nitrogen and sulfur atom in the ring is, for example, pyridine ring, furan ring, thiophene ring, quinoline ring, pyrazole ring, imidazole ring, thiazole ring, triazole ring, benzofuran ring, thianaphthalene ring, indole ring and benzimidazole ring. Among the above examples, pyridine ring, furan ring, thiophene ring and quinoline ring are preferable and pyridine ring is especially preferable.

[0066] Examples of the C5-C10 straight or branched-chain saturated or unsaturated hydrocarbon group substituted by these aromatic rings are 4-pyridylmethyl group, 3-furanylmethyl group, 3-thiophenylethyl group, 2-quioline-4-ylmethyl group and 3-pyridylethyl group and especially preferably 4-pyridylmethyl group.

[0067] The monocyclic or bicyclic aromatic ring containing one or more hetero-atoms selected from oxygen, nitrogen and sulfur atom in the ring may be substituted by a substituent L, and such substituent L is selected from C1-C6 alkyl group, halogen atom, —NO2 and —CN, for example, methyl group, ethyl group, isobutyl group, 1-ethylpropyl group, chloro group, bromo group, nitro group and nitrile group and, among the above examples, methyl group, ethyl group and chloro group are preferable.

[0068] The groups R10, R11, R12, R13, R14, R15, R16 and R17 are each independently hydrogen atom, a C1-C6 straight or branched-chain alkyl group which may have substituent, a C7-C11 aralkyl group which may have substituent, a C6-C10 aryl group which may have substituent (these substituents are halogen atom, OH, C1-C4 alkoxy group, —CN, —NO2 or —COOR18), or a group selected from the formula (4)-1, the formula (4)-2 and the formula (4)-3 or R10 and R11, or R13 and R14 together form a 3 to 12-membered ring which may contain one or more —O—, —S—, —NR18— or —(C═O)— groups in the ring. Preferable examples of the groups R10, R11, R12, R13, R14, R15, R16 and R17 are hydrogen atom, a C1-C6 straight or branched-chain alkyl group which may have substituents, a C7-C11 aralkyl group which may have substituents, a C6-C10 aryl group which may have substituents (these substituents are C1-C4 alkoxy group or COOR18) or a group selected from the formula (4)-1, the formula (4)-2 and the formula (4)-3. 9

[0069] When these groups are hydrogen atom, a C1-C6 straight or branched-chain alkyl group which may have substituents, a C7-C11 aralkyl group which may have substituents or a C6-C10 aryl group which may have substituents, examples of the groups are hydrogen atom, methyl group, ethyl group, isopropyl group, n-butyl group, pentyl group, hexyl group, benzyl group, phenyl group and naphthyl group, preferably methyl group, ethyl group, benzyl group and phenyl group. These group may be substituted by halogen atom, —OH, a C1-C4 alkyl group, —CN, —NO2 or —COOR18, and the substituent is preferably —Cl, —OH, ethoxy group, —CN or —COOH.

[0070] When the groups R10 and R11 or R13 and R14 together form a 3 to 12-membered ring, the ring may contain O, S or NR18. Concretely, the ring is e.g. pyrrolidine ring, piperidine ring, pyrrolidone ring, piperazine ring, morpholine ring, thiomorpholine ring, etc., and above all, pyrrolidine ring, piperidine ring, piperazine ring and morpholine ring are preferable. When the ring is e.g. piperazine ring, the nitrogen atom of the ring may be substituted by a C1-C4 lower alkyl group, i.e. R18, and in this case, the substituent is especially preferably methyl group or isopropyl group.

[0071] In the formula (3)-1 or the formula (3)-2, the group X3 is —(C═O)—, —O—, —S—, —(S═O)—, —(O═S═O)—, —NR21, *—NR21(C═O)— or *—(C═O)NR2 (the sign (*—) representing a bond means the bonding to the benzene ring or the naphthalene ring). The group is e.g. —(C═O)—, —O—, —S—, —N(CH3)(C═O)— or —(C═O)NCH3 and especially preferably —O— or —S—.

[0072] In the formula (4)-1, the formula (4)-2 and the formula (4)-3, the group Q is a C2-C10 alkyl group which may have substituents, a non-substituted C1-C6 alkenyl group which may have substituents, a C1-C6 alkoxy group which may have substituents, a C7-C11 aralkyl group which may have substituents, a C7-C11 aralkyloxy group which may have substituents, dimethylamino group, morpholino group or a monocyclic or bicyclic aromatic hydrocarbon group which may contain one or plural hetero-atoms selected from oxygen, nitrogen and sulfur atom in the ring.

[0073] When the group Q is a C1-C10 alkyl group which may have substituents, a C1-C6 alkenyl group which may have substituents, a C1-C6 alkoxy group which may have substituents, a C7-C11 aralkyl group which may have substituents, a C7-C11 aralkyloxy group which may have substituents, the concrete examples of the group are methyl group, ethyl group, propyl group, heptyl group, methoxy group, allyl group, benzyl group, phenylpropyl group and benzyloxy group. These groups may be substituted by halogen atom, —OH, —CN, —NO2, —COOR19 or phenoxy group. Concretely, preferable substituent is chloro group, —OH, —COOH or phenoxy group.

[0074] When the group Q is a monocyclic or bicyclic aromatic hydrocarbon group which may contain one or plural hetero-atoms selected from oxygen, nitrogen and sulfur atoms in the ring, any one of the groups described in the following formula (10) can be selected as the aromatic hydrocarbon group. 10

[0075] These groups are bonded to the amide group, carboxyl group or sulfonyl group in the formula (4)-1, the formula (4)-2 or the formula (4)-3 as the group Q at an arbitrary possible position, and may be bonded with the following groups at the remaining positions. Namely, the groups may be substituted by one or plural groups independently selected from halogen atom, —OH, —NO2, —CN, —COOR19, —NR19R20, a straight or branched-chain C1-C6 alkyl group, a straight or branched-chain C1-C6 alkoxy group (in this case, an acetal bond may be formed at the sites adjacent to each other as the substituents), a straight or branched-chain C1-C6 alkylthio group, a straight or branched-chain C1-C6 alkylsulfonyl group, a straight or branched-chain C1-C6 acyl group, a straight or branched-chain C1-C6 acylamino group, trihalomethyl group, trihalomethoxy group, phenyl group, or phenoxy group which may be substituted by one or more halogen atoms. In the above description, R19 and R20 are each hydrogen atom or a C1-C4 lower alkyl group.

[0076] Concrete examples of preferable substituents are —COOH, —F, —Cl, —Br, —NO2, —OH, —NH2, —NHCH3, —N(CH3)2, —NH(C═O)CH3, —(C═O)CH3, —CF3, —OCF3, —CN, —OCH3, —Ph, —CH3, —(O═S═O)—, —CH3, —SCH3 and —OPh.

[0077] In the above formula (2), Y2 is the group of formula (3)-1, the formula (3)-2, the formula (5)-1 or the formula (5)-2. Among the groups expressed by the formula (3)-1 or the formula (3)-2, the preferable groups are, as mentioned before, the groups of the formula (9)-1, (9)-2 or (9)-3. 11

[0078] In the formula (5)-1 or the formula (5)-2, the group R7 is hydrogen atom or optionally substituted straight, branched or alicyclic C1-C12 saturated hydrocarbon group or unsaturated hydrocarbon group containing one or two double bonds or triple bonds [in this case, the substituent is halogen atom, —NO2, —CN, an optionally substituted phenyl group (the substituent is halogen atom, —NO2, —CN, —CF3 or a C1-C4 hydrocarbon group) or an optionally substituted 5 to 8-membered cycloalkyl group (the substituent is halogen atom or a C1-C4 hydrocarbon group)].

[0079] Each of the above groups has a total carbon number of 1 to 12 including the substituents. The cyclic saturated hydrocarbon group or unsaturated hydrocarbon group having one or two double bonds or triple bonds does not include aromatic rings such as benzene ring and hetero-aromatic ring, and the ring is directly bonded to the group X4 in the formula (5)-1 or the formula (5)-2. That is to say, the cyclic means alicyclic. In other words, these rings are free from oxygen, sulfur, nitrogen atom and carbonyl group in the ring, and the preferable examples of the ring are cyclopropane ring, cyclobutane ring, cyclopentane ring, cydohexane ring, cyclooctane ring, cycloheptane ring, cyclododecane ring, norbornene ring and cyclohexene ring. Cyclopentane ring, cyclohexane ring, cyclooctane ring and cyclododecane ring are more preferable among the above examples.

[0080] The straight-chain saturated hydrocarbon group or unsaturated hydrocarbon group having one or two double bonds or triple bonds is, for example, methyl group, ethyl group, n-propyl group, n-butyl group, n-hexyl group, n-octyl group, n-dodecyl group, 2-propenyl group, 3-butenyl group, 4-hexenyl group, 3-hexenyl group, 3-nonenyl group, 2,4-hexadienyl group and 2-propynyl group, preferably methyl group, ethyl group, n-propyl group, n-butyl group, n-hexyl group, 2-propenyl group, 3-butenyl group, 4-hexenyl group, 3-hexenyl group, 2,4-hexadienyl group or 2-propynyl group.

[0081] The branched saturated or unsaturated hydrocarbon group is, for example, isopropyl group, t-butyl group, ethylpropyl group, ethylpentyl group, 4-methylpentyl group, 2-ethylbutyl group, 2-methylpropyl group, 2-methylbutyl group, 2,4,4-trimethylpentyl group, 2-methylheptyl group, 3-methyl-1-(2-methylpropyl)butyl group, 2-methyl-1-(methylethyl)propyl group, 3-methyl-3-butenyl group, 3-methyl-2-butenyl group, 1-vinyl-2-propenyl group, 4-methyl-3-pentenyl group, 1-allyl-3-butenyl group, 1-ethyl-2-propenyl group, 1-propyl-2-propenyl group and 1-ethyl-2-propynyl group. Symmetric groups are preferable among the above groups. Especially preferable groups are ethylpropyl group and 2-ethylbutyl group.

[0082] The substituent of R7 is halogen atom, —NO2, —CN, a substituted or non-substituted phenyl group (the substituent is selected from halogen atom, —NO2, —CN, —CF3 and C1-C4 hydrocarbon group) and a substituted or non-substituted 5 to 8-membered cycloalkyl group (the substituent is selected from halogen atom and a C1-C4 hydrocarbon group).

[0083] In the substituent of Rthe substituted or non-substituted phenyl group (the substituent is selected from halogen atom, —NO2, —CN, —CF3 and a C1-C4 hydrocarbon group) is, for example, phenyl group, m-fluorophenyl group, p-chlorophenyl group, m-iodophenyl group, p-fluorophenyl group, 2,4-dichlorophenyl group, 3,5-difluorophenyl group, p-nitrophenyl group, m-nitrophenyl group, p-methylthiophenyl group, o-cyanophenyl group, p-cyanophenyl group, m-trifluoromethylphenyl group, p-methylphenyl group, p-isopropylphenyl group, p-t-butylphenyl group and 3,4-dimethylphenyl group.

[0084] The 5 to 8-membered cycloalkyl group as the substituent of the group R7 may be substituted by halogen atom or C1-C4 hydrocarbon group. Preferable examples of the C1-C4 hydrocarbon group are methyl group and ethyl group. Namely, examples of the optionally substituted 5 to 8-membered cycloalkyl group are cyclopentyl group, cyclohexyl group, cycloheptyl group, cyclooctyl group, 2-chlorocyclohexyl group, 2-methylcydohexyl group, 2-ethylcyclohexyl group, 3-methylcyclohexyl group, 4-methylcydohexyl group, 4-(i-propyl)cyclohexyl group, 2,6-dimethylcyclohexyl group and 3,5-dimethylcyclohexyl group.

[0085] The group R7 is preferably hydrogen atom, a straight or branched-chain C1-C12 saturated hydrocarbon group or unsaturated hydrocarbon group having one or two double bonds or triple bonds and optionally substituted by halogen atom, or a group expressed by the following formulas. 12

[0086] [in the formula, n1 is an integer of 1 to 3, n3 is an integer of 0 to 3, n2 is an integer of 0 to 9 (when n3 is 0) or an integer of 2 to 5 (when n3 is an integer of 1 to 3), R26 and R27 are each independently hydrogen atom, halogen atom, NO2, CN, CF3 or a C1-C4 hydrocarbon group, and R28 is hydrogen atom or a C1-C4 hydrocarbon group]. (The groups R26 and R27 are more preferably hydrogen atom, halogen atom or NO2).

[0087] The group R7 is especially preferably hydrogen atom or a group selected from the groups expressed by the following formula (12). 13

[0088] The group X4 in the formula (5)-1 or the formula (5)-2 is —(C═O)—, —O—, —S—, —(S═O)—, —(O═S═O)—, —NR23—, *—NR23(C═O)— or *—(C═O)NR23. (The sign (−) representing a bond is bonded to the benzene ring or the naphthalene ring having R8 and R9, R23 is hydrogen atom or a C1-C4 hydrocarbon group which may be substituted by halogen atom. R1 is not hydrogen atom when X4 is —(C═O)—, —S═O)—, (O═S═O)— or *—NR23(C═O)—.). X4 is preferably —O—, —S—, —(S═O)— or —(O═S═O)—, more preferably —O— or —S— and especially preferably —O—.

[0089] R23 is preferably hydrogen atom, methyl group or ethyl group, especially preferably hydrogen atom.

[0090] In the formula (5)-1 and the formula (5)-2, the groups R8 and R9 are each independently hydrogen atom, halogen atom, —NO2, —CO2H, —CN, —OR24, —NH(C═O)R24, —(C═O)NHR24 or a straight or branched-chain saturated or unsaturated C1-C4 hydrocarbon group which may be substituted by halogen atom (the group R24 is hydrogen atom or a C1-C3 hydrocarbon group which may be substituted by halogen atom.). It is preferably hydrogen atom, halogen atom, —NO2, —CN, —OH, —OCH3, —NH(C═O)CH3, —(C═O)NHCH3 or a straight or branched-chain saturated or unsaturated C1-C4 hydrocarbon group which may be substituted by halogen atom. It is more preferably hydrogen atom, halogen atom, —CH3, —OCH3, —OH, ethyl group, isopropyl group, t-butyl group, allyl group or trifluoromethyl group, further preferably hydrogen atom, halogen atom, —CH3, —OCH3, —OH or trifluoromethyl group and especially preferably hydrogen atom.

[0091] When the group R24 is a C1-C3 hydrocarbon group which may be substituted by halogen, it is, for example, methyl group, ethyl group, isopropyl group and trifluoromethyl group and preferably methyl group or trifluoromethyl group.

[0092] In the formula (1) or the formula (2), X1 is —(C═O)—, —O—, —S., —(SO)—, —(O═S═O)— or —CH2—, preferably —O—, —S—, —(S═O)— or —(O═S═O)—, especially preferably —O— or —S—.

[0093] In the formula (1) or the formula (2), X2 is O or S, preferably O.

[0094] In the formula (1) or the formula (2), R1 and R2 are each independently hydrogen atom, halogen atom, —NO2, —CO2H, —CN, —OR25, —NH(C═O)R25, —(C═O)NHR25 or a C1-C4 straight or branched-chain saturated or unsaturated hydrocarbon group which may be substituted by halogen atom. Concrete examples' of the groups are hydrogen atom, chloro group, bromo group, —NO2, —CO2H, —CN, methoxy group, ethoxy group, chloromethoxy group, butoxy group, acetylamide group, propionylamide group, methylaminocarbonyl group, butylaminocarbonyl group, methyl group, bromoethyl group, allyl group and chloropropenyl group, and preferably hydrogen atom, halogen atom (especially chloro group), —OH, —NO2, —CO2H, —CN, methoxy group, chloromethoxy group, acetylamide group, methylaminocarbonyl group or methyl group.

[0095] In the formula (1) or the formula (2), R3 and R4 are each independently hydrogen atom or a C1-C4 hydrocarbon group. Concrete examples of the groups are hydrogen atom, methyl group, ethyl group, propyl group and butyl group and preferably hydrogen atom or methyl group.

[0096] In the formula (1) or the formula (2), n is an integer of 0 to 3, preferably 0 or 1.

[0097] In the formula (2), A is N, NO or N+—CH3, preferably N or N→O, more preferably N.

[0098] The anthranilic acid derivative of the present invention or its pharmacologically permissible salt can be converted into solvate at need. The solvent usable in the conversion process is water, methanol, ethanol, (n- or i-)propyl alcohol, (n- or t-)butanol, acetonitrile, acetone, methyl ethyl ketone, chloroform, ethyl acetate, diethyl ether, t-butyl methyl ether, benzene, toluene, DMSO, DMF, etc., preferably water, methanol, ethanol, (n- or i-)propyl alcohol or acetonitrile.

[0099] When the compound of the formula (1) or the formula (2) has CO2H group in the molecule, the anthranilic acid derivative of the present invention can be converted as necessary into a non-toxic cation salt or its solvate. Examples of such salt are alkali metal ion such as Na+ and K+, alkaline earth metal ion such as Mg2+ and Ca2+, metal ion such as Al3+ and Zn2+, or organic base such as ammonia, triethylamine, ethylenediamine, propanediamine, pyrrolidine, piperidine, piperazine, pyridine, lysine, choline, ethanolamine, N,N-dimethylethanolamine, 4-hydroxypiperidine, glucosamine, and N-methylglucamine, preferably Na+, Ca2+, lysine, choline, N,N-dimethylethanolamine and N-methylglucamine. The solvents for forming the solvates of these salts are, for example, water, methanol, ethanol, (n- or i-)propyl alcohol, (n- or t-)butanol, acetonitrile, acetone, methyl ethyl ketone, chloroform, ethyl acetate, diethyl ether, t-butyl methyl ether, benzene, toluene, DMF and DMSO, especially preferably water, methanol, ethanol, (n- or i-)propyl alcohol and acetonitrile.

[0100] When the compound of the formula (1) or the formula (2) contains primary, secondary or tertiary amine group in the molecule, the anthranilic acid derivative of the present invention can be converted as necessary into an acid addition salt or its solvate. The acid for the production of the acid addition salt is a mineral acid such as hydrochloric acid, sulfuric acid and nitric acid or an organic acid such as acetic acid, benzoic acid, fumaric acid, maleic acid, methanesulfonic acid and toluenesulfonic acid. Preferable acids among the above examples are hydrochloric acid, sulfuric acid, acetic acid, fumaric acid, maleic acid, methanesulfonic acid and toluenesulfonic acid. The solvent for the production of the solvate of the salt is, for example, water, methanol, ethanol, (n- or i-)propyl alcohol, (n- or t-)butanol, acetonitrile, acetone, methyl ethyl ketone, chloroform, ethyl acetate, diethyl ether, t-butyl methyl ether, benzene, toluene, DMF and DMSO, and preferably water, methanol, ethanol, (n- or i-)propyl alcohol and acetonitrile.

[0101] Concrete preferable examples of the compounds expressed by the formula (1) or the formula (2) of the present invention are compounds described in the Table 1 to the Table 43, their pharmacologically permissible salts or their solvates.

TABLE 1
1  14
2  15
3  16
4  17
5  18
6  19
7  20
8  21
9  22
10 23
11 24
12 25
13 26
14 27
15 28
16 29
17 30
18 31
19 32
20 33
21 34
22 35
23 36
24 37
25 38
26 39
27 40
28 41
29 42
30 43

[0102]

TABLE 2
31 44
32 45
33 46
34 47
35 48
36 49
37 50
38 51
39 52
40 53
41 54
42 55
43 56
44 57
45 58
46 59
47 60
48 61
49 62
50 63
51 64
52 65
53 66
54 67
55 68
56 69
57 70
58 71
59 72

[0103]

TABLE 3
60 73
61 74
62 75
63 76
64 77
65 78
66 79
67 80
68 81
69 82
70 83
71 84
72 85
73 86
74 87
75 88
76 89
77 90
78 91
79 92
80 93
81 94
82 95
83 96
84 97
85 98
86 99
87 100

[0104]

TABLE 4
88  101
89  102
90  103
91  104
92  105
93  106
94  107
95  108
96  109
97  110
98  111
99  112
100 113
101 114
102 115
103 116
104 117
105 118
106 119
107 120
108 121
109 122
110 123
111 124
112 125
113 126
114 127
115 128
116 129
117 130

[0105]

TABLE 5
118 131
119 132
120 133
121 134
122 135
123 136
124 137
125 138
126 139
127 140
128 141
129 142
130 143
131 144
132 145
133 146
134 147
135 148
136 149
137 150
138 151
139 152
140 153
141 154
142 155
143 156
144 157
145 158
146 159
147 160

[0106]

TABLE 6
148 161
149 162
150 163
151 164
152 165
153 166
154 167
155 168
156 169
157 170
158 171
159 172
160 173
161 174
162 175
163 176
164 177
165 178
166 179
167 180
168 181
169 182
170 183
171 184
172 185
173 186
174 187
175 188
176 189
177 190

[0107]

TABLE 7
178 191
179 192
180 193
181 194
182 195
183 196
184 197
185 198
186 199
187 200
188 201
189 202
190 203
191 204
192 205
193 206
194 207
195 208
196 209
197 210
198 211
199 212
200 213
201 214
202 215
203 216
204 217
205 218
206 219
207 220

[0108]

TABLE 8
208 221
209 222
210 223
211 224
212 225
213 226
214 227
215 228
216 229
217 230
218 231
219 232
220 233
221 234
222 235
223 236
224 237
225 238
226 239
227 240
228 241
229 242
230 243
231 244
232 245
233 246
234 247
235 248
236 249
237 250

[0109]

TABLE 9
238 251
239 252
240 253
241 254
242 255
243 256
244 257
245 258
246 259
247 260
248 261
249 262
250 263
251 264
252 265
253 266
254 267
255 268
256 269
257 270
258 271
259 272
260 273
261 274
262 275
263 276
264 277
265 278
266 279
267 280

[0110]

TABLE 10
268 281
269 282
270 283
271 284
272 285
273 286
274 287
275 288
276 289
277 290
278 291
279 292
280 293
281 294
282 295
283 296
284 297
285 298
286 299
287 300
288 301
289 302
290 303
291 304
292 305
293 306
294 307
295 308
296 309
297 310

[0111]

TABLE 11
298 311
299 312
300 313
301 314
302 315
303 316
304 317
305 318
306 319
307 320
308 321
309 322
310 323
311 324
312 325
313 326
314 327
315 328
316 329
317 330
318 331
319 332
320 333
321 334
322 335
323 336
324 337
325 338
326 339
327 340

[0112]

TABLE 12
328 341
329 342
330 343
331 344
332 345
333 346
334 347
335 348
336 349
337 350
338 351
339 352
340 353
341 354
342 355
343 356
344 357
345 358
346 359
347 360
348 361
349 362
350 363
351 364
352 365
353 366
354 367
355 368
356 369
357 370

[0113]

TABLE 13
358 371
359 372
360 373
361 374
362 375
363 376
364 377
365 378
366 379
367 380
368 381
369 382
370 383
371 384
372 385
373 386
374 387
375 388
376 389
377 390
378 391
379 392
380 393
381 394
382 395
383 396
384 397
385 398
386 399
387 400

[0114]

TABLE 14
388 401
389 402
390 403
391 404
392 405
393 406
394 407
395 408
396 409
397 410
398 411
399 412
400 413
401 414
402 415
403 416
404 417
405 418
406 419
407 420
408 421
409 422
410 423
411 424
412 425
413 426
414 427
415 428
416 429
417 430

[0115]

TABLE 15
418 431
419 432
420 433
421 434
422 435
423 436
424 437
425 438
426 439
427 440
428 441

[0116]

TABLE 16
429 442
430 443
431 444
432 445
433 446
434 447
435 448
436 449
437 450
438 451
439 452
440 453
441 454
442 455
443 456
444 457
445 458
446 459
447 460
448 461
449 462
450 463
451 464
452 465
453 466
454 467
455 468
456 469
457 470
458 471

[0117]

TABLE 17
459 472
460 473
461 474
462 475
463 476
464 477
465 478
466 479
467 480
468 481
469 482
470 483
471 484
472 485
473 486
474 487
475 488
476 489
477 490
478 491
479 492
480 493
481 494
482 495
483 496
484 497
485 498
486 499
487 500
488 501

[0118]

TABLE 18
489 502
490 503
491 504
492 505
493 506
494 507
495 508
496 509
497 510
498 511
499 512
500 513
501 514
502 515
503 516
504 517
505 518
506 519
507 520
508 521
509 522
510 523
511 524
512 525
513 526
514 527
515 528
516 529
517 530
518 531

[0119]

TABLE 19
519 532
520 533
521 534
522 535
523 536
524 537
525 538
526 539
527 540
528 541
529 542
530 543
531 544
532 545
533 546
534 547
535 548
536 549
537 550
538 551
539 552
540 553
541 554
542 555
543 556
544 557
545 558
546 559
547 560
548 561

[0120]

TABLE 20
549 562
550 563
551 564
552 565
553 566
554 567
555 568
556 569
557 570
558 571
559 572
560 573
561 574
562 575
563 576
564 577
565 578
566 579
567 580
568 581
569 582
570 583
571 584
572 585
573 586
574 587
575 588
576 589
577 590
578 591

[0121]

TABLE 21
579 592
580 593
581 594
582 595
583 596
584 597
585 598
586 599
587 600
588 601
589 602
590 603
591 604
592 605
593 606
594 607
595 608
596 609
597 610
598 611
599 612
600 613
601 614
602 615
603 616
604 617
605 618
606 619
607 620
608 621

[0122]

TABLE 22
609 622
610 623
611 624
612 625
613 626
614 627
615 628
616 629
617 630
618 631
619 632
620 633
621 634
622 635
623 636
624 637
625 638
626 639
627 640
628 641
629 642
630 643
631 644
632 645
633 646
634 647
635 648
636 649
637 650
638 651

[0123]

TABLE 23
639 652
640 653
641 654
642 655
643 656
644 657
645 658
646 659
647 660
648 661
649 662
650 663
651 664
652 665
653 666
654 667
655 668
656 669
657 670
658 671
659 672
660 673
661 674
662 675
663 676
664 677
665 678
666 679
667 680
668 681

[0124]

TABLE 24
669 682
670 683
671 684
672 685
673 686
674 687
675 688
676 689
677 690
678 691
679 692
680 693
681 694
682 695
683 696
684 697
685 698
686 699
687 700
688 701
689 702
690 703

[0125]

TABLE 25
691 704
692 705
693 706
694 707
695 708
696 709
697 710
698 711
699 712
700 713
701 714
702 715
703 716
704 717
705 718
706 719
707 720
708 721
709 722
710 723
711 724
712 725
713 726
714 727
715 728
716 729
717 730
718 731
719 732
720 733

[0126]

TABLE 26
721 734
722 735
723 736
724 737
725 738
726 739
727 740
728 741
729 742
730 743
731 744
732 745
733 746
734 747
735 748
736 749
737 750
738 751
739 752
740 753
741 754
742 755
743 756
744 757
745 758
746 759
747 760
748 761
749 762
750 763

[0127]

TABLE 27
751 764
752 765
753 766
754 767
755 768
756 769
757 770
758 771
759 772
760 773
761 774
762 775
763 776
764 777
765 778
766 779
767 780
768 781
769 782
770 783
771 784
772 785
773 786
774 787
775 788
776 789
777 790
778 791

[0128]

TABLE 28
779 792
780 793
781 794
782 795
783 796
784 797
785 798
786 799
787 800
788 801
789 802
790 803
791 804
792 805
793 806
794 807
795 808
796 809
797 810
798 811
799 812
800 813
801 814
802 815

[0129]

TABLE 29
803 816
804 817
805 818
806 819
807 820
808 821
809 822
810 823
811 824
812 825
813 826
814 827
815 828
816 829
817 830
818 831
819 832
820 833
821 834
822 835
823 836
824 837
825 838
826 839
827 840
828 841
829 842
830 843
831 844

[0130]

TABLE 30
832 845
833 846
834 847
835 848
836 849
837 850
838 851
839 852
840 853
841 854
842 855
843 856
844 857
845 858
846 859
847 860
848 861
849 862
850 863
851 864
852 865
853 866
854 867
855 868
856 869
857 870
858 871
859 872
860 873
861 874

[0131]

TABLE 31
862 875
863 876
864 877
865 878
866 879
867 880
868 881
869 882
870 883
871 884
872 885
873 886
874 887
875 888
876 889
877 890
878 891
879 892
880 893
881 894
882 895
883 896
884 897
885 898
886 899
887 900
888 901
889 902
890 903

[0132]

TABLE 32
891 904
892 905
893 906
894 907
895 908
896 909
897 910
898 911
899 912
900 913
901 914
902 915
903 916
904 917
905 918
906 919
907 920
908 921
909 922
910 923
911 924
912 925
913 926
914 927
915 928
916 929
917 930
918 931

[0133]

TABLE 33
919 932
920 933
921 934
922 935
923 936
924 937
925 938
926 939
927 940
928 941
929 942
930 943
931 944
932 945
933 946
934 947
935 948
936 949
937 950
938 951
939 952
940 953
941 954
942 955
943 956
944 957
945 958
946 959
947 960
948 961

[0134]

TABLE 34
949 962
950 963
951 964
952 965
953 966
954 967
955 968
956 969
957 970
958 971
959 972
960 973
961 974
962 975
963 976
964 977
965 978
966 979
967 980
968 981
969 982
970 983
971 984
972 985
973 986
974 987
975 988
976 989
977 990
978 991
979 992
980 993

[0135]

TABLE 35
981  994
982  995
983  996
984  997
985  998
986  999
987  1000
988  1001
989  1002
990  1003
991  1004
992  1005
993  1006
994  1007
995  1008
996  1009
997  1010
998  1011
999  1012
1000 1013
1001 1014
1002 1015
1003 1016
1004 1017
1005 1018
1006 1019
1007 1020
1008 1021
1009 1022
1010 1023

[0136]

TABLE 36
1011 1024
1012 1025
1013 1026
1014 1027
1015 1028
1016 1029
1017 1030
1018 1031
1019 1032
1020 1033
1021 1034
1022 1035
1023 1036
1024 1037
1025 1038
1026 1039
1027 1040
1028 1041
1029 1042
1030 1043
1031 1044
1032 1045
1033 1046
1034 1047
1035 1048
1036 1049
1037 1050
1038 1051
1039 1052
1040 1053

[0137]

TABLE 37
1041 1054
1042 1055
1043 1056
1044 1057
1045 1058
1046 1059
1047 1060
1048 1061
1049 1062
1050 1063
1051 1064
1052 1065
1053 1066
1054 1067
1055 1068
1056 1069
1057 1070
1058 1071
1059 1072
1060 1073
1061 1074
1062 1075
1063 1076
1064 1077
1065 1078
1066 1079
1067 1080
1068 1081
1069 1082
1070 1083

[0138]

TABLE 38
1071 1084
1072 1085
1073 1086
1074 1087
1075 1088
1076 1089
1077 1090
1078 1091
1079 1092
1080 1093
1081 1094
1082 1095
1083 1096
1084 1097
1085 1098
1086 1099
1087 1100
1088 1101
1089 1102
1090 1103
1091 1104
1092 1105
1093 1106
1094 1107
1095 1108
1096 1109
1097 1110
1098 1111
1099 1112
1100 1113

[0139]

TABLE 39
1101 1114
1102 1115
1103 1116
1104 1117
1105 1118
1106 1119
1107 1120
1108 1121
1109 1122
1110 1123
1111 1124
1112 1125
1113 1126
1114 1127
1115 1128
1116 1129
1117 1130
1118 1131
1119 1132
1120 1133
1121 1134
1122 1135
1123 1136
1124 1137
1125 1138
1126 1139
1127 1140
1128 1141
1129 1142
1130 1143

[0140]

TABLE 40
1131 1144
1132 1145
1133 1146
1134 1147
1135 1148
1136 1149
1137 1150
1138 1151
1139 1152
1140 1153
1141 1154
1142 1155
1143 1156
1144 1157
1145 1158
1146 1159
1147 1160
1148 1161
1149 1162
1150 1163
1151 1164
1152 1165
1153 1166
1154 1167
1155 1168
1156 1169
1157 1170
1158 1171
1159 1172
1160 1173

[0141]

TABLE 41
1161 1174
1162 1175
1163 1176
1164 1177
1165 1178
1166 1179
1167 1180
1168 1181
1169 1182
1170 1183
1171 1184
1172 1185
1176 1186
1181 1187
1182 1188
1184 1189
1185 1190
1186 1191
1187 1192
1188 1193
1189 1194
1190 1195

[0142]

TABLE 42
1191 1196
1192 1197
1193 1198
1194 1199
1195 1200
1196 1201
1197 1202
1198 1203
1199 1204
1200 1205
1201 1206
1202 1207
1203 1208
1204 1209
1205 1210
1206 1211
1207 1212
1208 1213
1209 1214
1210 1215
1211 1216
1212 1217
1213 1218
1214 1219
1215 1220
1216 1221
1217 1222
1218 1223
1219 1224
1220 1225

[0143]

TABLE 43
1221 1226
1222 1227
1223 1228
1224 1229
1225 1230
1226 1231
1227 1232
1228 1233
1229 1234
1230 1235
1231 1236
1232 1237
1233 1238
1234 1239
1235 1240
1236 1241
1237 1242
1238 1243
1239 1244
1240 1245
1241 1246
1242 1247
1243 1248
1244 1249
1245 1250
1246 1251

[0144] The anthranilic acid derivative of the present invention has strong cytotoxic activity and/or IgE antibody production suppressing activity. Concretely, as for cytotoxic activity, LC50 or GI50 is 5,000 nM or less, preferably 0.05 nM to 1,000 nM, more preferably 0.05 nM to 500 nM. As for IgE antibody production suppressing activity, IC50 is 1,000 nM or less, preferably 0.05 nM to 500 nM, more preferably 0.05 M to 100 nM.

[0145] The anthranilic acid derivative of the present invention having such an excellent cytotoxic activity can be used as a therapeutic agent clinically applicable to cancer. Since the anthranilic acid derivative of the present invention further has excellent IgE antibody production suppressing activity, compounds having relatively weak cytotoxicity among the above compounds are rather suitable for the use as a preventing agent and/or therapeutic agent clinically applicable to various allergic diseases.

[0146] The derivative of the present invention expressed by the aforementioned formula (1) or formula (2) or its pharmacologically permissible salt can be produced for example according to the following scheme. 12521253

[0147] Namely, an aryl derivative [I] or [VI] having a group expressed by Z1X3 or Z1X4 (Z1 is hydrogen atom, a general protecting group such as benzyl group, benzoyl group, methoxymethyl group, acetyl group or trimethylsilyl group, the group Z defined in the formula (3)-1 and the formula (3)-2 or the group R7 defined in the formula (5)-1 or the formula (5)-2) and a carboxylic acid group is coupled with an anthranilic acid derivative [II] under a proper condition to enable the production of the compounds [III] and [VII] from the starting compounds [I] and [VI], respectively. The group Z1 of the produced compound [III] or [VII] is deprotected to obtain respective intermediate [IV] or [VIII] and a side chain Z is introduced into the compound [IV] to obtain the compound [V] or a side chain Z or a group R7 is introduced into the compound [VIII] to obtain a compound [IX]. When the group —CO2R3 is an ester, the product can be converted as necessary into a carboxylic acid by hydrolyzing the ester of the compound [V] or [IX]. When the group Z1 in the compound [III] or [VII] is Z or R7 defined before, the compound [III] or [VII] becomes the objective compound [V] or [IX], respectively, and when the group —CO2R3 is an ester, the ester [III] and [VII] can be converted as necessary into a carboxylic acid by hydrolysis.

[0148] The definitions of the groups A, Z, X1 to X4, R1 to R9 and n in the above formulas are same as the definitions in the formulas (1), (2), (3)-1, (3)-2, (5)-1 and (5)-2. There is no restriction on the production process of the starting substances [I] and [VI], and these compounds can be produced by known conventional methods.

[0149] The compounds [V] and [IX] are concretely synthesizable as follows.

[0150] The condensation of the compound [I] or [VI] to the compound [II] can be roughly classified into a method through an acid halide and an activation method without passing through an acid halide and either method is principally a known method.

[0151] In the case of passing through an acid halide, the objective compounds [III] and [VII] can be produced from the compounds [I] and [II] and the compounds [VI] and [II], respectively, by treating the compound [I] or [VI] with a proper halogenation agent such as oxalyl chloride and thionyl chloride in the presence or absence of an additive such as DMF in a proper solvent (e.g. methylene chloride or tetrahydrofuran) and reacting the produced acid halide with the compound [II] in the presence or absence of a proper base (e.g. triethylamine or potassium carbonate).

[0152] In the activation method which does not go through an acid halide, the objective compounds [III] and [VII] can be produced from the compounds [I] and [II] and the compounds [VI] and [II], respectively, by activating the compound [I] or [VI] with a proper activation agent such as mixed acid anhydride, carbodnmides, imidazolation agent, halophosphoric acid esters or cyanophosphoric acid esters in a proper solvent (e.g. methylene chloride or tetrahydrofuran) and reacting the activated compound with the compound [II].

[0153] The group Z1 in Z1X3 of the compounds [III] and [VII] may be Z and in Z2X4 may be R1 itself. When X3 is —O—, —S—, —NR21 or —(C═O)NR21 (in this case, the carbonyl group is bonded to the benzene ring or naphthalene ring in the formula (3)-1 or the formula (3)-2, and the definition of R21 is same as the definition in the formula (3)-1 and the formula (3)-2) or X4 is —O—, —S—, —NR23— or —(C═O)NR23 (in this case, the carbonyl group is bonded to the benzene ring or naphthalene ring in the formula (5)-1 or the formula (5)-2 and the definition of R23 is same as the definition in the formula (5)-1 and the formula (5)-2), the compound [IV] or [VIII] can be used as an intermediate after deprotection by using a proper protecting group (for example, ethers of benzyl group, allyl group, etc., silyl ethers of t-butyldimethylsilyl group, etc., esters of benzoyl group, etc., carbonates such as allyl carbonate, etc. when X3 or X4 is —O—; thioethers of benzyl group, etc., thioesters of benzoyl group, etc., thiocarbonates of t-butyl carbonate, etc. when it is —S—; benzyl group, formyl group, etc. when it is —NR21— or —NR23—; and t-butyldimethylsilyloxy group, methylthio group, etc. when it is —(C═O)NR21 or —(C═O)NR23), and the compound [V] can be produced by introducing Z into the compound [IV] or the compound [IX] can be produced by introducing Z or R7 into the compound [VIII] to facilitate the development of synthesis. For example, when X3 or X4 in the compound [III] or [VII] is —O—, the debenzylated intermediate [IV] or [VIII] can be produced from the compound [III] or [VII] by hydrogenation by the use of benzyl group as the group Z1. Further, the introduction of Z into the compound [IV] gives the compound [V] and the introduction of Z or R7 into the compound [VIII] gives the compound [IX]. In this case, R3 is preferably a C1-C4 hydrocarbon group among the groups defined in the formula (1) and the formula (2) from the viewpoint of the handling in synthesis. In other words, the compound of the formula (1) or formula (2) wherein R3 is hydrogen atom is produced preferably by introducing the group Z into the intermediate [IV] or introducing the group Z or the group R7 into the intermediate [VIII] and hydrolyzing the group CO2R3 (i.e. the group R3 is a C1-C4 hydrocarbon group).

[0154] There is no particular restriction on the method for introducing the group Z of the formula (3)-1 and the formula (3)-2 or the group R7 of the formula (5)-1 and the formula (5)-2 into the compound [IV] or [VIII], and the introduction can be carried out for example by using a reactant ZX5, R7X5, etc. An alcohol and an alkyl halide are concrete examples of ZX6 or R7X6 when X3 and X4 are —O—. The objective compound [V] containing introduced group Z or the compound [IX] containing introduced group Z or R7 can be produced, in the case of using an alcohol as the ZX5 or R7X5, by using ZOH or R7OH, triphenyl phosphine (which may be replaced with tributyl phosphine, etc.), diethyl azodicarboxylate [which may be replaced with diisopropyl azodicarboxylate or 1,1-azobis(N,N-dimethylformamide)] and carrying out Mitsunobu synthesis or its analogous reaction in a proper solvent (e.g. N-methylmorpholine or tetrahydrofuran) at a proper temperature condition. In the case of using an alkyl halide, etc., ire. using a halogen atom as the eliminable group X5, the objective compound [V] or [IX] can be produced by carrying out the reaction in the presence of a proper base such as sodium hydride, potassium carbonate or triethylamine in a proper solvent (e.g. dimethylformamide, tetrahydrofuran, acetonitrile or methylene chloride) under a proper temperature condition.

[0155] When the group X3 is —NR21 or the group X4 is —NR23, the group Z in the formula (3)-1 or the formula (3)-2 or the group R7 in the formula (5)-1 or the formula (5)-2 can be introduced by the above reaction similar to the case that the group X3 or X4 is —O—. When the group X3 or X4 is —S—, the compound ZX5 is an alkyl halide derivative, etc. In the case of synthesizing a compound containing —NH—, —NH2—, —CO2H, —OH, —SH, etc., in the group Z of the compound [V] or [IX] and further containing a substituent introduced into these functional groups, a compound of formula Z2X5 (there is no particular definition of Z2, however, it is a group produced by introducing a proper protecting group into —NH, —NH2, —CO2H, —OH or —SH in the side chain) having proper protecting group introduced into —NH, —NH2, —CO2H, —OH or —SH is synthesized beforehand, the synthesized compound is made to react with the compound [IV] or [VIII] by the aforementioned method to introduce the group Z2, the protecting group of —NH—, —NH2, —CO2H, —OH or —SH in the group Z2 is removed, the product is used as an intermediate and various substituents are introduced into the intermediate to obtain the objective new compound having the group Z. When the group —CO2R3 is an ester, it can be induced as necessary into a carboxylic acid compound by hydrolyzing the ester —CO2R3.

[0156] Concrete example of the synthesizing process is the protection of the amino group of trans-4-aminocyclohexanol with benzyl group beforehand to obtain a dibenzyl compound, Mitsunobu reaction of the product with an intermediate [IV] or [VIII], debenzylation of the product to obtain an amino compound and the reaction with a reagent having a group to be introduced, for example, an acid chloride, sulfonyl chloride, etc., to obtain an amide compound, a sulfonamide compound, etc., as the objective compound. When the group —CO2R3 is an ester, a carboxylic acid compound can be produced as necessary by hydrolyzing the group —CO2R3 Also in this case, the group R3 is preferably a C1-C4 lower hydrocarbon group among the above definition in the formula (1) and the formula (2) from the viewpoint of handleability in synthesis, namely, a compound wherein R3 is hydrogen atom is preferably produced by the hydrolysis of —CO2R3.

[0157] A compound of the formula (1) or (2) wherein X1, X3 and X4 are each —(S═O)— or —(O═S═O)— or A is N→O can be produced by oxidizing a corresponding compound wherein X1, X3 or X4 are S or A is N. Although there is no particular restriction on the stage for oxidizing S or N in the above case, the objective oxidized product can be produced e.g. by oxidizing the non-oxidized compound [V] or [IX] with a general oxidizing agent such as peroxide or NBS.

[0158] A compound of the formula (1) or (2) wherein X3 or X4 is —(C═O)— can be synthesized e.g. by introducing ZCO or R7CO by Friedel-Crafts reaction at an arbitrary reaction stage. As an alternative, in the case of using a compound having carboxylic acid group at a position corresponding to the X3 or X4 on the benzene ring or naphthalene ring of the formula (3)-1, (3)-2, (5)-1 or (5)-2, the carboxylic acid can be converted into a ketone by activating the carboxylic acid with carbodmidazole, etc., converting into an amide with N-methoxy-N-methylamine and reacting with a Grignard reagent of group Z or group R7 or lithium anion. When a raw material having carboxylic acid group at a position corresponding to the group X3 or X4 of the formula (3)-1, (3)-2, (5)-1 or (5)-2 is unavailable, a compound having methyl group, aldehyde group or —CH2OH at the corresponding position can be converted into carboxylic acid by oxidization. A compound having cyano group at the corresponding group can be converted into carboxylic acid by the hydrolysis of the cyano group. Further, even a compound having only hydrogen atom at the corresponding position can be converted into a carboxylic acid e.g. by the carboxylation with carbon dioxide.

[0159] When the group X3 is —NR21(C═O) or the group X4 is —NR23(C═O) (in this case, the N of —NR21(C═O) is bonded to the benzene ring or naphthalene ring in the formula (3)-1 or the formula (3)-2 and the N of —NR23(C═O) is bonded to the benzene ring or naphthalene ring in the formula (5)-1 or the formula (5)-2. The definition of R21 is same as the one shown in the formula (3)-1 and the formula (3)-2 and that of R23 is same as the one shown in the formula (5)-1 and the formula (5)-2.), the objective compound [V] or [IX] can be synthesized by reacting, at an arbitrary reaction stage, the compound [IV] or [VIII] with an acid chloride of the compound of the formula ZCO2H or its activated product in the case that the group —X3H of the compound [IV] or [VIII] is —NHR21 or reacting the compound [VIII] with an acid chloride of the formula R7CO2H or ZCO2H or its activated product in the case that the group —X4H of the compound [VIII] is —NHR23.

[0160] When the group X3 is —(C═O)NR21 or the group X4 is —(C═O)NR23 (in this case, the carbonyl group of —(C═O)NR21 is bonded to the benzene ring or naphthalene ring in the formula (3)-1 or the formula (3)-2 and the carbonyl group of —(C═O)NR23 is bonded to the benzene ring or naphthalene ring in the formula (5)-1 or the formula (5)-2. The definition of R21 is same as the one expressed in the formula (3)-1 and the formula (3)-2 and that of R23 is same as the one expressed in the formula (5)-1 and the formula (5)-2.), the objective compound can be synthesized by coupling, at an arbitrary reaction stage, a corresponding amine with a compound produced by activating a carboxylic acid with carbodinimdazole or oxalyl chloride, etc., using a compound having carboxylic acid group at a position corresponding to the X3 or the X4 of the formula (3)-1, the formula (3)-2, the formula (5)-1 or the formula (5)-2.

[0161] When the group R4 is an alkyl group, the objective compound is synthesized, although there is no restriction on the synthesis method, preferably by N-alkylating an anthranilic acid derivative [II] with a general alkylation agent, e.g. an alkyl halide such as an alkyl iodide before the coupling of the derivative with a compound [I] or [VI] in the above scheme and then coupling the alkylation product with the compound [I] or [VI].

[0162] Although there is no particular restriction on the process for the synthesis of the compounds [I] and [VI] which are raw materials for the above scheme, these compounds can be synthesized with reference to the description of the International Application WO95/32943 and the International Application 97/19910 or by the following method.

[0163] In the case of n is zero, these compounds can be synthesized according to the following scheme. 12541255

[0164] In the above scheme, the definitions of R5, R6, R8, R9, X1, X3, X4 and A are same as the definitions in the formula (1), the formula (2), the formula (3)-1, the formula (3)-2, the formula (5)-1 and the formula (5)-2. The definition of Z1 is same as the aforementioned definition. The group R26 is hydrogen atom or a C1-C4 hydrocarbon group. As shown in the above scheme, these compounds can be produced by coupling the compound [X], [XI], [XII] or [XIII] having X7 as a nucleophilic site with the compound [XIV] or [XVI] having a proper eliminable group such as halogen atom on X8 using a proper base reagent and a proper solvent, concretely, the compound [XV] can be synthesized by coupling the compound [X] or [XI] with the compound [XIV] and the compound [XVII] can be synthesized by coupling the compound [X], [XI], [XII] or [XIII] with the compound [XVI]. When the group R26 is a hydrocarbon group, the compound [XV] and [XVII] can be converted into the corresponding carboxyhic acid [I] and [VI] by the hydrolysis of the ester. Concretely, it can be synthesized by the following method.

[0165] In the case of producing the compound [XV] by the reaction of the compound [X] or [XI] with the compound [XIV] and in the case that the group XI is —O— or —S—, the objective compound [XV] can be synthesized by reacting the compound [X] or [XI] wherein X7 is —OH or —SH with the compound [XIV] wherein X8 is F in the presence of a proper base reagent such as potassium carbonate (other examples of the reagent are sodium carbonate, potassium bicarbonate, etc.) in a proper solvent such as N,N-dimethylacetamide (other examples of the solvent are N,N-dimethylformamide, tetrahydrofuran, methylene chloride, etc.) under a proper temperature condition comprising the reaction at room temperature or under heating. In the above case, the group R26 of the compound [XIV] is preferably a C1-C4 hydrocarbon group from the viewpoint of the handleability in synthesis. In other words, it is preferable to obtain the carboxylic acid [I] by the ester hydrolysis of the compound [XV].

[0166] In the case of producing the compound [XVII] by the reaction of the compound [X], [XI], [XII] or [XIII] and in the case that the group X1 is —O— or —S—, the compound [XVII] can be synthesized by reacting the compound [X], [XI], [XII] or [XIII] wherein the group X7 is —OH or —SH with the compound [XVI] wherein the group X8 is —Cl in the presence of a proper base reagent such as sodium hydride (other examples of the reagent are potassium carbonate, sodium carbonate and potassium bicarbonate) in a proper solvent such as N,N-dimethylformamide under a proper temperature condition comprising the reaction at 0° C. or under heating. Also in the above case, the group R26 of the compound [XVI] is preferably a C1-C4 hydrocarbon group from the viewpoint of the handleability in synthesis. In other words, it is preferable to obtain the carboxylic acid [VI] by the ester hydrolysis of the compound [XVII].

[0167] In the case of n is 1, these compounds can be synthesized according to the following scheme. 12561257

[0168] In the above scheme, the definitions of R5, R6, R8, R9, X1, X3, X4 and A are same as the definitions in the formula (1), the formula (2), the formula (3)-1, the formula (3)-2, the formula (5)-1 and the formula (5)-2, and the definition of Z1 is same as aforementioned definition. As shown in the above scheme, these compound can be produced by coupling the compound [X], [XI], [XII] or [XIII] having X7 as a nucleophilic site with the compound [XVIII] or [XXI] having a proper eliminable group such as halogen atom on the group X8 using a proper base reagent and a proper solvent to synthesize the compound [XIX] from the compound [α]or [XI] or synthesize the compound [XXII] from the compound [X], [XI], [XII] or [XIII] and the product is subjected to rearrangement reaction to synthesize the thioamide [XX] from the compound [XIX] or synthesize the compound [XXIII] from the compound [XXII]. Furthermore, the products [XX] and [XXIII] can be converted into the compounds [I] and [VI] by hydrolysis. Concretely, the synthesis can be performed as follows.

[0169] In the case of producing the compound [XIX] by the reaction of the compound [X] or [XI] with the compound [XVIII] and in the case that the group X1 is —O— or —S—, the objective compound [XIX] can be synthesized by reacting the compound [X] or [XI] wherein X7 is —OH or —SH with the compound [XVIII] wherein X8 is —F in the presence of a proper base reagent such as potassium carbonate (other examples of the reagent are sodium carbonate, potassium bicarbonate and sodium hydride) in a proper solvent such as N,N-dimethylacetamide under a proper temperature condition comprising the reaction at room temperature or under heating. The product can be converted into the compound [I] by heating in the presence of S and morpholine to effect the rearrangement reaction and hydrolyzing the resultant thioamide [XX].

[0170] In the case of producing the compound [XXII] by the reaction of the compound [X], [XI], [XII] or [XIII] and in the case that the group XI is —O— or —S—, the compound [XXII] can be synthesized by reacting the compound [X], [XI], [XII] or [XIII] wherein the group X7 is —OH or —SH with the compound [XXI] wherein the group X8 is —Cl in the presence of a proper base reagent such as sodium hydride (other examples of the reagent are potassium carbonate, sodium carbonate and potassium bicarbonate) in a proper solvent such as N,N-dimethylformamide under a proper temperature condition comprising the reaction at 0° C. or under heating. The product can be converted into the compound [VI] by heating in the presence of S and morpholine to effect the rearrangement reaction and hydrolyzing the resultant thioamide [XXIII].

[0171] Although there is no particular restriction on the process for the synthesis of the compounds [I] and [VI] wherein n is 2 or 3 and XI is —O— or —S—, these compounds can be synthesized with reference to a coupling method described in the paper of Journal of Medicinal Chemistry vol.40, no.4, sections 395-407 (1997) or similar methods.

[0172] Similarly, the compounds [I] and [VI] wherein n is 0 or 3 and X1 is —(C═O)— or —CH2— can be synthesized, although there is no restriction on the process, with reference to a coupling method described in the paper of Journal of Medicinal Chemistry vol.40, no.4, sections 395-407 (1997) or similar methods.

[0173] The anthranilic acid derivative of the present invention and its pharmacologically permissible salt can be administered by peroral means or parenteral means such as intravenous injection, subcutaneous injection, intramuscular injection, transcutaneous administration, rectal infusion, nasal administration, eye instillation or by inhalation.

[0174] The form of the oral administration drug is, for example, tablet, pill, granule, powder, liquid, suspension, syrup or capsule.

[0175] A tablet can be formed by conventional method using an excipient such as lactose, starch and crystalline cellulose, a binder such as carboxymethylcellulose, methylcellulose and polyvinylpyrrolidone, a disintegrant such as sodium alginate, sodium bicarbonate and sodium laurylsulfate; etc.

[0176] A pill, granule and powder are also formable by conventional method using the above excipients, etc.

[0177] A liquid agent, suspension and syrup can be formed by conventional method using a glycerol ester such as tricaprylin and triacetin; an alcohol such as ethanol; water; a vegetable oil such as corn oil, cottonseed oil, coconut oil, almond oil, peanut oil and olive oil; etc.

[0178] A capsule can be formed by filling a granule, powder or liquid agent into a capsule made of gelatin, etc.

[0179] The agent for intravenous, subcutaneous or intramuscular administration is, for example, an injection composed of an aseptic aqueous or non-aqueous solution agent. The aqueous solution agent is produced e.g. by using physiological salt solution. The non-aqueous solution agent is produced e.g. by using propylene glycol, polyethylene glycol, a vegetable oil such as olive oil, an injectable organic ester such as ethyl oleate, etc. These drugs may be incorporated as necessary with isotropic agent, antiseptic agent, wetting agent, emulsifying agent, dispersing agent, stabilizing agent, etc., and asepticized by proper treatments such as filtration through a bacteria-retaining filter, compounding of a disinfectant, heating treatment, irradiation treatment, etc. As an alternative, it can be used by preparing an aseptic solid preparation and dissolving the agent in aseptic water or an aseptic solvent for injection immediately before use.

[0180] The agent for percutaneous administration is an ointment agent, a cream agent, etc. These agents can be produced by conventional method using an oil and fat such as castor oil or olive oil or petrolatum, etc., for an ointment agent and a fatty oil, diethylene glycol, an emulsifier such as sorbitan monofatty acid ester, etc., for a cream agent.

[0181] A conventional suppository such as gelatin soft capsule is used for the rectal administration.

[0182] The preparation for transnasal administration is supplied in the form of a liquid or powdery composition. The base for the liquid agent is water, salt solution, phosphate buffer solution, acetate buffer solution, etc., and the agent may further contain a surfactant, an antioxidant, a stabilizer, a preservative and a thickening agent. The base for the powdery agent is preferably a water-absorbing material, for example, easily water-soluble polyacrylic acid salts such as sodium polyacrylate, potassium polyacrylate and ammonium polyacrylate; cellulose lower alkyl ethers such as methylcellulose, hydroxyethylcellulose, hydroxypropylcellulose and carboxymethylcellulose sodium; polyethylene glycol polyvinylpyrrolidone, amylose, pullullan etc.; celluloses such as a scarcely water-soluble crystalline cellulose, a cellulose and crosslinked carboxymethylcellulose sodium; starches such as hydroxypropyl starch, carboxymethyl starch, crosslinked starch, amylose, amylopectin and pectin; proteins such as gelatin, casein and casein sodium; gums such as gum arabic, tragacanth gum and glucomannan; crosslinked vinyl polymers such as polyvinylpolypyrrolidone, crosslinked polyacrylic acid and its salt, crosslinked polyvinyl alcohol and polyhydroxyethyl methacrylate; etc., or their mixture. The powdery agent may be incorporated further with an antioxidant, a colorant, a preservative, an antiseptic agent, a decay modifying agent, etc. Such liquid agent and powdery agent can be administered e.g. by using a spraying tool.

[0183] The eye instillation agent is an aqueous or non-aqueous instillation. The aqueous instillation can be produced by using sterilized pure water, physiological salt solution or proper aqueous solvent as the solvent, and includes an aqueous eye drop produced by using only a sterilized pure water as the solvent; a viscous eye drop added with a thickening agent such as carboxymethylcellulose, methylcellulose, hydroxypropylcellulose and polyvinylpyrrolidone; an aqueous suspension eye drop added with a surfactant or a suspension agent such as, a polymer thickener; a solubilized eye drop added with a solubilizing agent such as a nonionic surfactant; etc. The non-aqueous instillation uses a non-aqueous solvent for injection as the solvent and includes a non-aqueous eye drop produced by using vegetable oil, liquid paraffin, mineral oil, propylene glycol, etc.; a non-aqueous suspension eye drop produced by using a thixotropic colloid such as aluminum monostearate as a suspension agent; etc. These preparations may be incorporated as necessary with an isotonic agent, a preservative, a buffer agent, an emulsifier, a stabilizing agent, etc., or asepticized by proper treatments such as filtration through a bacteria-retaining filter, compounding of a disinfectant, heating treatment, irradiation treatment, etc. As an alternative, it can be used by preparing an aseptic solid preparation and dissolving or suspending the agent in a proper aseptic solution immediately before use.

[0184] The dosage form for the administration to the eye other than an ophthalmic instillation is an eye ointment formed by using petrolatum, etc.; an application liquid produced by using dilute iodine tincture, zinc sulfate solution, methyl chloride rosaniline liquid, etc.; a scattering agent to directly apply fine powder of active component; an insertion agent produced by compounding or impregnating an active component in a proper base or a material and used by inserting into the eyelid, etc.

[0185] A solution or suspension of an active component and a conventional excipient for medicine is used for the inhalation, for example, in the form of an aerosol spray for inhalation. As an alternative, an active component having dried powdery form is administered by an inhalator or other device to enable the direct contact of the active component with the lung.

[0186] The administration dose of the compound of the present invention depends upon the kind of disease, administration path, condition, age, sex, body weight, etc., of the patient, etc. It is about 0.1 to 1,000 mg/day/head, preferably 1 to 300 mg/day/head in oral administration and about 0.1 to 100 mg/day/head, preferably 0.1 to 30 mg/day/head in parenteral administration such as intravenous, subcutaneous, intramuscular, percutaneous, rectal or nasal administration, ophthalmic instillation and inhalation, and the drug is prepared preferably to satisfy the above condition.

[0187] In the case of using the compound of the present invention as a preventing agent, such preparations may be administered beforehand according to each symptom by the administration method known as a method for the administration of preventing agent.

[0188] As shown in the following Examples, the anthranilic acid derivative of the present invention is effective for suppressing the highly proliferative L929 cell at a low concentration. Since the derivative is also effective for suppressing the proliferation of various other human cancer cells at a low concentration, it is extremely useful as a carcinostatic agent. Furthermore, as shown in the following Examples, the derivative also suppresses the production of IgE antibody from human lymphocyte by an antigen non-specific stimulation (IL-4+IL-10 (interleukin 10)+antiCD40Ab (anti-CD40 antibody)). Accordingly, the anthranilic acid derivative of the present invention is useful also as a preventive and/or therapeutic agent for allergic diseases caused by the production of IgE antibody such as bronchial asthma, allergic rhinitis, allergic conjunctivitis, atopic dermatitis, anaphylactic shock, mite allergy, pollinosis, food allergy, urticaria, ulcerative colitis, eosinophilic gastroenteritis and drug-induced rash.

EXAMPLES

[0189] The present invention is explained concretely by the following Reference Examples and Examples. The experiment was performed on the following group of compounds, however, the present invention is not restricted by these Examples. The 1H-NMR peaks originated from carboxylic acid, hydroxyl group, amine or amide were sometimes unobservable. Although it is not particularly described, the amine compound may take the form of hydrochloride.

[0190] When the following Reference Example or Example contains the sentence of “the following compound was synthesized by a similar method using the corresponding substrate”, the used reagent was synthesized by the use of a substrate analogized from the product. In the case that the judgement by analogy was difficult, the substrate was clearly described in some Examples. The reaction temperature, the reaction time and the purification method are different to an extent among these reactions.

Reference Example 1

[0191] Synthesis of 1-(4-(6-benzyloxy-2-naphthyloxy)phenyl)ethan-1-one 1258

[0192] 4-Fluoroacetophenone (969 μl, 8.00 mmol) was added to dry N,N-dimethylacetamide (12 ml) solution of 6-benzyloxy-2-naphthol (500 mg, 2.00 mmol) and potassium carbonate (553 mg, 4.00 mmol) in nitrogen atmosphere and stirred at 150° C. for 5 hours. After completing the reaction, 10% citric acid was added to the reaction liquid, extracted with methylene chloride, washed with water, dried with magnesium sulfate and concentrated. The obtained residue was purified by silica gel chromatography to obtain the subject compound (707 mg, 1.92 mmol). The result of 1H-NMR was consistent with the above structure.

[0193] Yield: 96%

[0194] 1 H-NMR (CDCl3); δ 7.94 (d, 2H, J=8.88 Hz), 7.76 (d, 1H, J=8.91 Hz), 7.68 (d, 1H, J=9.88 Hz), 7.51-7.19 (m, 9H), 7.02 (d, 2H, J=8.91 Hz), 5.19 (s, 2H), 2.57 (s, 3H).

Reference Example 2

[0195] The following compounds were synthesized by a method similar to the Reference Example 1 using substrates corresponding to respective compounds. The results of 1H-NMR were consistent with the above structures.

[0196] 1-(4-(4-Benzyloxyphenoxy)phenyl)ethan-1-one

[0197] Yield: 73%

[0198] 1 H-NMR (CDCl3): δ 2.56 (s, 3H), 5.07 (s, 2H), 6.97 (m, 6H), 7.42 (m, 5H), 7.91 (m, 2H).

[0199] 4-(4-Benzyloxyphenyloxy)benzoic Acid Methyl Ester

[0200] Yield: 55%

[0201] 1 H-NMR (CDCl3); δ 7.97 (d, 2H, J=8.90 Hz), 7.31-7.46 (m, 5H), 7.00 (s, 4H), 6.93 (d, 2H, J=8.90 Hz), 5.07 (s, 2H), 3.89 (s, 3H).

[0202] In this case, 4-fluorobenzoic acid methyl ester was used in place of 4-fluoroacetophenone.

Reference Example 3

[0203] Synthesis of 1-(moroholin-4-yl)-2-(4-(6-benzyloxyphenoxy-2-naphthyloxy)phenyl)ethane-1-thione 1259

[0204] The 1-(4-(6-benzyloxy-2-naphthyloxy)phenyl)ethan-1-one (3.6 g, 9.77 mmol) obtained by the Reference Example 1 was dissolved in morpholine (15 ml) in nitrogen atmosphere, added with sulfur (1.57 g, 48.8 mmol) and stirred at 120° C. for 18 hours. After completing the reaction, methanol was added to the reaction liquid and the formed precipitate was filtered to obtain the subject compound (3.73 g, 7.94 mmol) as the precipitate. The result of 1H-NMR was consistent with the above structure.

[0205] Yield: 81%

[0206] 1 H-NMR (CDCl3); δ 7.72 (d, 1H, J=8.91 Hz), 7.63 (d, 1H, J=9.88 Hz), 7.50-7.18 (m, 11H), 6.99 (d, 2H, J=8.59 Hz), 5.18 (s, 2H), 4.36 (t, 2H, J=4.94 Hz), 4.33 (s, 2H), 3.76 (t, 2H, J=4.78 Hz), 3.67 (t, 2H, J=4.94 Hz), 3.46 (t, 2H, J=4.78 Hz).

Reference Example 4

[0207] The following compound was synthesized by a method similar to the Reference Example 3 using the corresponding substrate. The result of 1H-NMR was consistent with the structure.

[0208] 1-(Moroholin-4-yl)-2-(4-(4-benzyloxy)phenoxy)phenyl)ethane-1-thione.

[0209] Yield: 84%

[0210] 1 H-NMR (CDCl3); δ 7.23-7.46 (m, 7H), 6.96 (m, 6H), 5.05 (s, 2H), 4.34 (m, 2H), 4.30 (s, 2H), 3.74 (m, 2H), 3.64 (m, 2H), 3.45 (m, 2H).

Reference Example 5

[0211] Synthesis of 4-(6-benzyloxy-2-naphthoxy)phenylacetic Acid 1260

[0212] An aqueous solution (10 ml) of 50% sodium hydroxide was added to 70% ethanol solution (50 ml) of the 1-(morpholin-4-yl)-2-(4-(6-benzyloxyphenoxy-2-naphthyloxy)phenyl)-ethane-thione (3.73 g, 7.94 mmol) obtained by the Reference Example 3 and the mixture was stirred at 100° C. for a night. After completing the reaction, the reaction liquid was added with 6N hydrochloric acid to adjust the pH to about 2, extracted with ethyl acetate, washed with water, dried with magnesium sulfate and concentrated. The obtained crude product was recrystallized from acetonitrile to obtain the subject compound (2.10 g, 5.46 mmol). The result of 1H-NMR was consistent with the above structure.

[0213] Yield: 69%

[0214] 1 H-NMR (DMSO-d6); δ 12.38 (br, 1H), 7.93 (d, 1H, J=8.91 Hz), 7.86 (d, 1H, J=8.88 Hz), 7.61-7.24 (m, 11H), 7.08 (d, 2H, J=8.48 Hz), 5.30 (s, 2H), 3.65 (s, 2H).

Reference Example 6

[0215] The following compound was synthesized by a method similar to the Reference Example 5 using a corresponding substrate. The result of 1H-NMR was consistent with the structure.

[0216] 4-(4-Benzyloxyphenoxy)phenylacetic Acid

[0217] Yield: 86%

[0218] 1 H-NMR (DMSO-d6); δ 12.12 (s, 1H), 7.31-7.14 (m, 5H), 7.06 (d, 2H, J=8.41 Hz), 6.85 (m, 4H), 6.70 (d, 2H, J=8.41 Hz), 4.92 (s, 2H), 3.36 (s, 2H).

Reference Example 7

[0219] Synthesis of 4-(6-benzyloxy-2-naphthyloxy)benzoic Acid 1261

[0220] 4-(6-Benzyloxy-2-naphthyloxy)benzoic acid ethyl ester (10.6 g, 26.2 mmol) was dissolved in a 2:1 mixture of THF and methanol (150 ml), added with 4N lithium hydroxide (33 ml) and stirred at room temperature. After completing the reaction, the reaction liquid was adjusted to pH 2 or thereabout with 1N hydrochloric acid, extracted with ethyl acetate, washed with water, dried with magnesium sulfate and concentrated to obtain the subject compound (8.70 g, 23.4 mmol). The result of 1H-NMR was consistent with the above structure.

[0221] Yield: 88%

[0222] 1 H-NMR (DMSO-d6); δ 12.79 (brs, 1H), 7.94 (d, 2H, J=8.91 Hz), 7.90 (d, 1H, J=8.91 Hz), 7.82 (d, 1H, J=8.91 Hz), 7.56-7.25 (m, 9H), 7.05 (d, 2H, J=8.74 Hz), 5.23 (s, 2H).

Reference Example 8

[0223] The following compound was synthesized by a method similar to the Reference Example 7 using a corresponding substrate. The result of 1H-NMR was consistent with the structure.

[0224] 4-(4-Benzyloxyphenyloxy)benzoic Acid

[0225] Yield: 89%

[0226] 1 H-NMR (DMSO-d6); δ 7.90 (d, 2H, J=8.91 Hz), 7.47-7.30 (m, 5H), 7.08 (s, 4H), 6.95 (d, 2H, J=8.91 Hz), 5.10 (s, 2H).

[0227] In this case, the methyl ester of the subject compound was used as the substrate.

Reference Example 9

[0228] Synthesis of 6-(4-benzyloxyphenoxy)-3-acetylpyridine 1262

[0229] Dried DMF solution (50 ml) of sodium hydride (60% in oil, 7.24 g, 181 mmol) was cooled with ice in nitrogen atmosphere, dried DMF solution (50 ml) of hydroquinone monobenzyl ether (36.2 g, 181 mmol) was dropped into the above solution spending 10 minutes under ice cooling and the mixture was stirred for 1.5 hours under ice cooling. Dried DMF solution (110 ml) of 6-chloro-3-acetylpyridine (26.7 g, 172 mmol) was dropped into the above mixture spending 15 minutes and stirred for 2 hours under ice cooling. After completing the reaction, the reaction liquid was acidified with 6N hydrochloric acid, added with water, extracted with ethyl acetate, washed with water (400 ml×3), dried with magnesium sulfate and concentrated. The residue was recrystallized from 2-propanol (300 ml) to obtain the subject compound (43.3 g, 136 mmol). The result of 1H-NMR was consistent with the above structure.

[0230] Yield: 75%

[0231] 1 H-NMR (CDCl3); δ 8.76 (d, 1H, J=2.64 Hz), 8.24 (dd, 1H, J-2.64, 8.58 Hz), 7.46-7.31 (m, 5H), 7.10-7.00 (m, 4H), 6.94 (d, 1H, J=8.58 Hz), 5.08 (s, 2H), 2.56 (s, 3H).

Reference Example 10

[0232] The following compounds were synthesized by a method similar to the Reference Example 9 using corresponding substrates. The results of 1H-NMR were consistent with the structures.

[0233] 6-(6-Benzyloxy-2-naphthyloxy)-3-acetylpyridine

[0234] Yield: 26%

[0235] 1 H-NMR (CDCl3); δ 2.57 (s, 3H), 5.20 (s, 2H), 7.01 (d, 1H, J=8.78 Hz), 7.79-7.14 (m, 11H), 8.27 (dd, 1H, J=2.44 Hz, 6.10 Hz), 8.76 (d, 1H, J=2.44 Hz).

[0236] 6-(4-Benzyloxyphenylthio)pyridine-3-carboxylic Acid Methyl Ester

[0237] Yield: 81%

[0238] 1 H-NMR (CDCl3); δ 8.81 (d, 1H, J=2.64 Hz), 8.25 (dd, 1H, J=2.31, 8.58 Hz), 7.46-7.31 (m, 5H), 7.08 (d, 2H, J=8.90 Hz), 7.02 (d, 2H, J=9.24 Hz), 6.90 (d, 1H, J=8.58 Hz), 5.07 (s, 2H), 3.91 (s, 3H).

[0239] In this case, 6-chloro-nicotinic acid methyl ester was used as the substrate in place of 6-chloro-3-acetylpyridine. Similar substrates were used in the synthesis of the following carboxylic acid methyl esters of the Reference Example 10.

[0240] 6-(4-Benzyloxyphenylthio)pyridine-3-carboxylic Acid Methyl Ester

[0241] Yield: 49%

[0242] 1 H-NMR (CDCl3); δ 8.81 (d, 1H, J=2.63 Hz), 8.27 (dd, 1H, J=2.31, 8.58 Hz), 7.55-7.16 (m, 6H), 7.05 (d, 2H, J=8.91 Hz), 6.92 (d, 1H, J=7.57 Hz), 6.71 (d, 1H, J=8.58 Hz), 4.11 (s, 2H), 3.92 (s, 3H).

[0243] 6-(4-(1-Ethylpropylthio)phenoxy)pyridine-3-carboxylic Acid Methyl Ester

[0244] Yield: 80%

[0245] 1 H-NMR (CDCl3); δ 8.83 (d, 1H, J=2.31 Hz), 8.28 (dd, 1H, J=1.97, 8.24 Hz), 7.45 (d, 2H, J=8.25 Hz), 7.08 (d, 2H, J=8.24 Hz), 6.94 (d, 1H, J=8.57 Hz), 3.92 (s, 3H), 2.96 (m, 1H), 1.63 (m, 4H), 1.03 (t, 6H, J=7.26 Hz).

[0246] 6-(2-Methyl-4-benzyloxyphenoxy)pyridine-3-carboxylic Acid Methyl Ester

[0247] Yield: 58%

[0248] 1 H-NMR (CDCl6); δ 8.81 (d, 1H, J=2.31 Hz), 8.25 (dd, 11H, J=2.31, 8.91 Hz), 7.47-7.31 (m, 5H), 6.99 (d, 1H, J=8.91 Hz), 6.91-6.83 (m, 3H), 5.05 (s, 2H), 3.91 (s, 3H), 2.12 (s, 3H).

[0249] 6-(3-Methyl-4-benzyloxyphenoxy)pyridine-3-carboxylic Acid Methyl Ester

[0250] Yield: 51%

[0251] 1 H-NMR (CDCl3); δ 8.82 (dd, 1H, J=0.66, 2.31 Hz), 8.25 (dd, 1H, J=2.31, 8.58 Hz), 7.47-7.31 (m, 5H), 6.96-6.87 (m, 4H), 5.08 (s, 2H), 3.91 (s, 3H), 2.29 (s, 3H).

Reference Example 11

[0252] Synthesis of 6-(4-benzyloxyphenoxy)pyridine-3-carboxylic Acid 1263

[0253] A THF—MEOH (2/1) solution (750 ml) of 6-(4-benzyloxyphenoxy)pyridine-3-carboxylic acid methyl ester (78.6 g, 234 mmol) obtained by the Reference Example 10 was added with 4N-lithium hydroxide solution (87.8 ml, 351 mmol) at room temperature (inner temperature: 15-20° C.) and stirred at room temperature (20-30° C.) for 4 hours. After completing the reaction, the reaction liquid was added with 10% aqueous solution of citric acid (600 ml) (inner temperature: 20-30° C.) to adjust the pH to about 4. The product was extracted with ethyl acetate (500 ml×3), washed with water (500 ml×1), dried with magnesium sulfate and concentrated. The residue was recrystallized from isopropanol (90 ml) to obtain the subject compound (59.9 g, 18.6 mmol). The result of 1H-NMR was consistent with the above structure.

[0254] Yield: 80%

[0255] 1 H-NMR (DMSO-d6); δ 13.14 (br, 1H), 8.65 (d, 1H, J=2.31 Hz), 8.26 (dd, 1H, J=2.31, 8.58 Hz), 7.48-7.31 (m, 5H), 7.13-7.03 (m, 5H), 5.12 (s, 2H).

Reference Example 12

[0256] The following compounds were synthesized by a method similar to the Reference Example 11 using corresponding substrates. The results of 1H-NMR were consistent with the structures.

[0257] 6-(4-Benzyloxyphenylthio)pyridine-3-carboxylic Acid

[0258] Yield: 94%

[0259] 1 H-NMR (DMSO-d6); δ 13.17 (br, 1H), 8.65 (d, 1H, J=2.31 Hz), 8.28 (dd, 1H, J=2.30, 8.57 Hz), 7.40-7.21 (m, 7H), 7.13-7.07 (m, 3H), 4.24 (s, 2H).

[0260] 6-(4-(1-Ethylpropylthio)phenoxy)pyridine-3-carboxylic Acid

[0261] Yield: 79%

[0262] 1 H-NMR (CDCl3); δ 8.90 (d, 1H, J=2.30 Hz), 8.33 (dd, 1H, J=2.31, 8.25 Hz), 7.45 (d, 2H, J=8.25 Hz), 7.09 (d, 2H, J=7.91 Hz), 6.97 (d, 1H, J=8.91 Hz), 2.96 (m, 1H), 1.63 (m, 4H), 1.02 (t, 6H, J=7.26 Hz).

[0263] 6-(2-Methyl-4-benzyloxyphenoxy)pyridine-3-carboxylic acid

[0264] Yield: 100%

[0265] 1 H-NMR (DMSO-d6); δ 8.59 (d, 1H, 1.98 Hz), 8.23 (dd, 1H, J=1.98, 8.57 Hz), 7.48-7.31 (m, 5H), 7.01-6.98 (m, 2H), 6.92 (d, 1H, J=8.57 Hz), 6.87 (dd, 1H, J=2.97, 8.58 Hz), 5.10 (s, 2H), 2.02 (s, 3H).

[0266] 6-(3-Methyl-4-benzyloxyphenoxy)pyridine-3-carboxylic Acid

[0267] Yield: 100%

[0268] 1 H-NMR (DMSO-d6); δ 8.61 (d, 1H, J=1.98 Hz), 8.22 (dd, 1H, J=1.98, 8.25 Hz), 7.50-7.31 (m, 5H), 7.05-6.98 (m, 4H), 5.13 (s, 2H), 2.21 (s, 3H).

Reference Example 13

[0269] Synthesis of N-methoxy-N-methyl(6-(4-benzyloxyphenoxy)-3-pyridyl)formamide 1264

[0270] Dried THF solution (300 ml) of 6-(4-benzyloxyphenoxy)pyridine-3-carboxylic acid (58.1 g, 181 mmol) obtained by the Reference Example 11 was cooled with ice (inner temperature 3° C.) in nitrogen atmosphere, oxalyl chloride (17.4 ml, 199 mmol) was dropped into the solution (inner temperature 3-7° C.) spending 7 minutes, and the mixture was added with DMF (3 ml) and stirred for 1 hour under ice cooling or at room temperature (3 to 20° C.). The reaction liquid was concentrated and dried by evacuating with a vacuum pump. The residual THF solution (300 ml) was cooled with ice (inner temperature 3° C.) in nitrogen atmosphere, N,O-dimethylhydroxylamine hydrochloride (21.2 g, 217 mmol) was added thereto, triethylamine (60 ml, 434 mmol) was dropped into the mixture (inner temperature 5-8° C.) and stirred over a night under ice cooling to room temperature (7-20° C.). After completing the reaction, the reaction liquid was added with water (400 ml), extracted with ethyl acetate (400 ml×3), washed with water (400 ml×3), dried with magnesium sulfate and concentrated. The residue was purified by silica gel chromatography to obtain the subject compound (54 g, 148 mmol). The result of 1H-NMR was consistent with the above structure.

[0271] Yield: 82%

[0272] 1 H-NMR (CDCl3); δ 8.63 (dd, 1H, J=0.66, 2.31 Hz), 8.08 (dd, 1H, J=2.31, 8.58 Hz), 7.47-7.30 (m, 5H), 7.11-6.94 (m, 4H), 6.90 (dd, 1H, J=0.66, 8.58 Hz), 5.07 (s, 2H), 3.57 (s, 3H), 3.37 (s, 3H).

Reference Example 14

[0273] The following compounds were synthesized by a method similar to the Reference Example 13 using corresponding substrates. The results of 1H-NMR were consistent with the structures.

[0274] N-Methoxy-N-methyl(6-(4-benzyloxyphenylthio)-3-pyridyl)formamide

[0275] Yield: 91%

[0276] 1 H-NMR (CDCl3); δ 8.63 (d, 1H, J=2.31 Hz), 8.10 (dd, 1H, J=2.31, 8.58 Hz), 7.65-7.21 (m, 6H), 7.09-7.02 (m, 3H), 6.92 (d, 1H, J=8.57 Hz), 4.11 (s, 2H), 3.57 (s, 3H), 3.38 (s, 3H).

[0277] N-Methoxy-N-methyl(6-(4-(1-ethylpropyllthio)phenoxy)-3-pyridyl)formamide

[0278] Yield: 85%

[0279] 1 H-NMR (CDCl3); δ 8.64 (d, 1H, J=2.31 Hz), 8.11 (dd, 1H, J=2.31, 8.58 Hz), 7.45 (d, 2H, J=8.58 Hz), 7.09 (d, 2H, J=8.57 Hz), 6.93 (d, 1H, J=8.57 Hz), 3.58 (s, 3H), 3.38 (s, 3H), 2.95 (m, 1H), 1.62 (m, 4H), 1.02 (t, 6H, J=7.26 Hz).

[0280] N-Methoxy-N-methyl(6-(2-methyl-4-benzyloxyphenoxy)-3-pyridyl)formamide

[0281] Yield: 72%

[0282] 1 H-NMR (CDCl3); δ 8.63 (d, 1H, J=2.31 Hz), 8.08 (ddd, 1H, J=0.66, 2.31, 8.58 Hz), 7.47-7.33 (m, 5H), 7.00 (d, 1H, J=8.58 Hz), 6.91-6.83 (m, 3H), 5.05 (s, 2H), 3.58 (s, 3H), 3.37 (s, 3H), 2.13 (s, 3H).

[0283] N-Methoxy-N-methyl(6-(3-methyl-4-benzyloxyphenoxy)-3-pyridyl)formamide

[0284] Yield: 66%

[0285] 1 H-NMR (CDCl3); δ 8.64 (d, 1H, J=2.31 Hz), 8.07 (dd, 1H, J=2.31, 8.58 Hz), 7.47-7.33 (m, 5H), 6.97-6.87 (4H), 5.09 (s, 2H), 3.58 (s, 3H), 3.37 (s, 3H), 2.30 (s, 3H).

Reference Example 15

[0286] Synthesis of 6-(4-benzyloxyphenoxy)-3-acetylpyridine 1265

[0287] Dried THF solution (250 ml) of N-methyl-N-methoxy(6-(4-benzyloxyphenoxy)-3-pyridyl)formamide (53.3 g, 147 mmol) obtained by the Reference Example 13 was cooled in a bath of −78° C. (inner temperature −70° C.) in nitrogen atmosphere, methyllithium (1.03 M/Et20, 171 ml, 176 mmol) was dropped into the solution spending 25 minutes (inner temperature −70 to −55° C.) and the mixture was stirred in a bath of −78° C. for 1 hour inner temperature −70 to −55° C.). After completing the reaction, the reaction liquid was added with methanol (20 ml) in cooled state and stirred for 3 minutes. The cooling bath was removed and saturated aqueous solution of ammonium chloride (300 ml) was added to the liquid. The product was extracted with ethyl acetate (200 ml×3), washed with water (200 ml×1), dried with magnesium sulfate and concentrated. The residue was recrystallized from isopropanol (300 ml) to obtain the subject compound (41.9 g, 131 mmol). The result of 1H-NMR was consistent with the above structure.

[0288] Yield: 89%

[0289] 1 H-NMR (CDCl3); δ 8.76 (d, 1H, J=2.64 Hz), 8.24 (dd, 11H, J=2.64, 8.58 Hz), 7.46-7.31 (<m, 5H), 7.10-7.00 (m, 4H), 6.94 (d, 1H, J=8.58 Hz), 5.08 (s, 2H), 2.56 (s, 3H).

Reference Example 16

[0290] The following compounds were synthesized by a method similar to the Reference Example 15 using corresponding substrates. The results of 1H-NMR were consistent with the structures.

[0291] 6-(4-Benzyloxyphenylthio)-3-acetylpyridine

[0292] Yield: 77%

[0293] 1 H-NMR (CDCl3); δ 8.75 (d, 1H, J=2.30 Hz), 8.26 (dd, 1H, J=2.31, 8.58 Hz), 7.37-7.21 (m, 7H), 7.06 (d, 2H, J=8.91 Hz), 6.96 (d, 1H, J=8.58 Hz), 4.12 (s, 2H), 2.57 (s, 3H).

[0294] 6-(4-(1-Ethylpropylthio)phenoxy)-3-acetylpyridine

[0295] Yield: 97%

[0296] 1 H-NMR (CDCl3); δ 8.77 (d, 1H, J=2.64 Hz), 8.26 (dd, 1H, J=2.31, 8.91 Hz), 7.45 (d, 2H, J=8.58 Hz), 7.08 (d, 2H, J=8.24 Hz), 6.97 (d, 1H, J=8.58 Hz), 2.96 (1.1H),2.57 (s, 3H), 1.63 (m, 4H), 1.03 (t, 6H, J=7.26 Hz).

[0297] 6-(2-Methyl-4-benzyloxyphenoxy) 3-acetylpyridine

[0298] Yield: 100%

[0299] 1 H-NMR (CDCl3); δ 8.75 (d, 1H, J=2.30 Hz), 8.24 (dd, 1H, J=2.30, 8.58 Hz), 7.47-7.31 (m, 5H), 6.99 (d, 1H, J=8.58 Hz), 6.94-6.83 (m, 4H), 5.05 (s, 2H), 2.56 (s, 3H), 2.12 (s, 3H).

[0300] 6-(3-Methyl-4-benzyoxyphenoxy)-3-acetylpyridine

[0301] Yield: 100%

[0302] 1 H-NMR (CDCl3); δ 8.76 (d, 1H, J=2.31 Hz), 8.23 (dd, 1H, J=2.31, 8.58 Hz), 7.47-7.33 (m, 5H), 6.97-6.91 (m, 4H), 5.09 (s, 2H), 2.56 (s, 3H), 2.30 (s, 3H).

Reference Example 17

[0303] Synthesis of 1-(morpholin-4-yl)-2-(6-(4-benzyloxyphenoxy)-3-pyridyl)ethane-1-thione 1266

[0304] Sulfur (8.21 g, 256 mmol) was added to a morpholine solution (200 ml) of 6-(4-benzyloxyphenoxy)-3-acetylpyridine (40.8 g, 128 mmol) obtained by the Reference Example 9 in nitrogen atmosphere and stirred for 5 hours in a bath of 120° C. After completing the reaction, the reaction liquid was concentrated and purified by silica gel chromatography to obtain the subject compound (30.6 g, 73 mmol). The result of 1H-NMR was consistent with the above structure.

[0305] Yield: 57%

[0306] 1 H-NMR (CDCl3); δ 8.03 (d, 1H, J=2.64 Hz), 7.78 (dd, 1H, J=2.64, 8.58 Hz), 7.45-7.30 (m, 5H), 7.08-6.98 (m, 4H), 6.86 (d, 1H, J=8.58 Hz), 5.06 (s, 2H), 4.33 (dd, 2H, J=4.94, 4.95 Hz), 4.24 (s, 2H), 3.75 (dd, 2H, J=4.62, 5.28 Hz), 3.67 (dd, 2H, J=4.29, 5.28 Hz), 3.51 (dd, 2H, J=4.29, 5.28 Hz).

Reference Example 18

[0307] The following compounds were synthesized by a method similar to the Reference Example 17 using corresponding substrates. The results of 1H-NMR were consistent with the structures.

[0308] 1-(Morpholin-4-yl)-2-(6-(6-benzyloxy-2-naphthyloxy)-3-pyridyl)ethane-1-thione

[0309] Yield: 45%

[0310] 1 H-NMR (CDCl3); δ 3.53 (m, 2H, J=2.64 Hz), 3.69 (m, 2H), 3.76 (m, 2H), 4.25 (s, 2H), 4.34 (m, 2H), 5.19 (s, 2H), 6.94 (d, 1H, J=8.58 Hz), 7.22-7.84 (m, 12H), 8.05 (d, 1H, J=2.48 Hz).

[0311] 2-(6-(4-(1-Ethylpropylthio)phenoxy)-3-pyridyl)-1-(morpholin-4-yl)ethane-1-thione

[0312] Yield: quant.

[0313] 1 H-NMR (CDCl3); δ 8.06 (d, 1H, J=2.31 Hz), 7.81 (dd, 1H, J=2.64, 8.58 Hz), 7.42 (d, 2H, J=8.58 Hz), 7.05 (d, 2H, J=8.58 Hz), 6.90 (d, 1H, J=8.58 Hz), 4.33 (m, 2H), 3.76 (m, 2H), 3.74 (s, 2H), 3.67 (m, 2H), 3.52 (m, 2H), 2.93 (m, 1H), 1.61 (m, 4H), 1.02 (t, 6H, J=7.26 Hz).

[0314] 2-(6-(2-Methyl-4-benzyloxyphenoxy)-3-pyridyl)-1-(morpholin-4-yl)ethane-1-thione

[0315] Yield: 84%

[0316] 1 H-NMR (CDCl3); δ 8.02 (d, 1H, J=2.31 Hz), 7.78 (dd, 1H, J=2.31, 8.58 Hz), 7.46-7.33 (m, 5H), 6.98 (d, 1H, J=8.58 Hz), 6.89 (d, 1H, J=2.64 Hz), 6.83 (d, 2H, J=8.58 Hz), 5.04 (s, 2H), 4.36-4.31 (m, 4H), 4.23 (s, 2H), 3.73-3.65 (, 2H), 3.52-3.48 (m, 2H), 2.12 (s, 3H).

[0317] 2-(6-(3-Methyl-4-benzyloxyphenoxy)-3-pyridyl)-1-(morpholin-4-yl)ethane-1-thione

[0318] Yield: 80%

[0319] 1 H-NMR (CDCl3); δ 8.03 (d, 1H, J=2.64 Hz), 7.77 (dd, 1H, J=2.64; 8.58 Hz), 7.46-7.27 (m, 5H), 6.95 (s, 1H), 6.89 (s, 2H), 6.85 (d, 1H, J=8.58 Hz), 5.07 (s, 2H), 4.34-4.31 (m, 4H), 4.23 (s, 2H), 3.68-3.65 (m, 2H), 3.53-3.49 (m, 2H), 2.28 (s, 3H).

Reference Example 19

[0320] Synthesis of 2-(6-(4-benzyloxyphenoxy)-3-pyridyl)acetic Acid 1267

[0321] 1-Morpholin-4-yl)-2-(6-(4-benzyloxyphenoxy)-3-pyridyl)ethane-1-thione (28.9 g, 71 mmol) obtained by the Reference Example 17 was dissolved in a mixture (2:1, 300 ml) of ethanol-30% aqueous solution of sodium hydroxide and stirred for 1 hour in a bath of 100° C. After completing the reaction, the reaction product was acidified by the addition of 50% aqueous solution of citric acid (250 ml), extracted with methylene chloride (250×3), washed with water, dried with magnesium sulfate and concentrated to obtain the subject compound (22.8 g, 68.0 mmol). The result of 1H-NMR was consistent with the above structure.

[0322] Yield: 96%

[0323] 1 H-NMR (CDCl3); δ 9.90 (br, 1H), 8.08 (s, 1H), 7.61 (dd, 1H, J=2.64, 8.58 Hz), 7.45-7.31 (m, 5H), 7.06-6.96 (m, 4H), 6.80 (d, 1H, J=8.58 Hz), 5.04 (s, 2H), 3.56 (s, 2H).

Reference Example 20

[0324] The following compounds were synthesized by a method similar to the Reference Example 19 using corresponding substrates. The results of 1H-NMR were consistent with the structures.

[0325] 2-(6-(6-Benzyloxy-2-naphthyloxy)-3-pyridyl) acetic Acid

[0326] Yield: 73%

[0327] 1 H-NMR (CDCl3); δ 3.62 (s, 2H), 5.18 (s, 2H), 6.92 (d, 1H, J=8.25 Hz), 7.23-7.76 (m, 12H), 8.10 (s, 1H).

[0328] 2-(6-(4-Benzyloxyphenylthio)-3-pyridyl)acetic Acid

[0329] Yield: 38%

[0330] 1 H-NMR (DMSO-d6); δ 12.44 (br, 1H), 8.01 (s, 1H), 7.74 (d, 1H, J=8.25 Hz), 7.38-7.21 (m, 7H), 7.05 (d, 2H, J=8.91 Hz), 6.97 (d, 1H, J=8.25 Hz), 4.22 (s, 2H), 3.58 (s, 2H).

[0331] 2-(6-(4-(1-Ethylpropylthio)phenoxy)-3-pyridyl)acetic Acid

[0332] Yield: 24% (two steps from the Reference Example 18)

[0333] 1 H-NMR (CDCl3); δ 10.34 (br, 1H), 8.12 (d, 1H, J=2.31 Hz), 7.66 (dd, 1H, J=2.31, 8.58 Hz), 7.42 (d, 2H, J=8.58 Hz), 7.04 (d, 2H, J=8.58 Hz), 6.86 (d, 1H, J=8.58 Hz), 3.60 (s, 2H), 2.93 (m, 1H), 1.61 (m, 4H), 1.01 (t, 6H, J=7.26 Hz).

[0334] 2-(6-(2-Methyl-4-benzyloxyphenoxy)-3-pyridyl)acetic Acid

[0335] Yield: 78%

[0336] 1 H-NMR (CDCl3); δ 8.03 (dd, 1H, J=2.64, 17.49 Hz), 7.62 (d, 1H, J=8.25 Hz, 7.45-7.30 (m, 5H), 6.97 (d, 1H, J=8.58 Hz), 6.89 (d, 1H, J=2.64 Hz), 6.84-6.78 (m, 2H), 5.04 (s, 2H), 2.14 (s, 2H), 2.08 (s, 3H).

[0337] 2-(6-(3-Methyl-4-benzyloxyphenoxy)-3-pyridyl)acetic Acid

[0338] Yield: 55%

[0339] 1 H-NMR (CDCl3); δ 8.08 (d, 1H, J=2.31 Hz), 7.62 (dd, 1H, J=2.31, 8.25 Hz), 7.46-7.30 (m, 5H), 6.94 (s, 1H), 6.90-6.89 (m, 2H), 6.83 (d, 1H, J=8.58 Hz), 5.07 (s, 2H), 3.60 (s, 2H), 2.28 (s, 3H).

Reference Example 21

[0340] Synthesis of 2-((4-(6-benzyloxy-2-naphthyloxy)phenyl)acetylamino)benzoic Acid Methyl Ester 1268

[0341] Oxalyl chloride (3.84 ml, 44.1 mmol) was dropped into a dry methylene chloride solution (200 ml) of 4-(6-benzyloxy-2-naphthoxy)phenylacetic acid (15.4 g, 4006 mmol) obtained by the Reference Example 5 in nitrogen atmosphere, 5 drops of DMF were added with a pipette and the mixture was stirred for 2.5 hours at 35 C. The reaction liquid was concentrated and the residue was dissolved in dry methylene chloride (200 ml). The obtained solution was dropped into a dry methylene chloride solution (200 ml) of methyl anthranylate (5.18 ml, 40.06 mmol) and triethylamine (6.14 ml, 44.1 mmol) under ice cooling in nitrogen atmosphere, and the mixture was stirred as it is for 1.5 hours and then for a night at room temperature. After completing the reaction, water is added to the reaction liquid, extracted twice with chloroform, washed with saturated sodium chloride solution, dried with anhydrous sodium sulfate and concentrated. The residue was purified by silica gel chromatography to obtain the subject compound (17.5 g, 33.8 mmol). The result of 1H-NMR was consistent with the above structure. Colorless acicular crystal.

[0342] Yield: 84%

[0343] 1 H-NMR (CDCl3); δ 3.75 (s, 2H), 3.88 (s, 3H), 5.17 (s, 2H), 7.02-7.11 (m, 3H), 7.20-7.26 (m, 3H), 7.32-7.56 (m, 9H), 7.62 (d, J=9.6 Hz, 1H), 7.70 (d, J=8.9 Hz, 1H), 8.01 (dd, J=1.7, 8.2 Hz, 1H), 8.73 (dd, J=1.0, 8.3 Hz, 1H), 11.08 (br.s, 1H).

Reference Example 22

[0344] The following compounds were synthesized by a method similar to the Reference Example 21 using corresponding substrates. The results of 1H-NMR were consistent with the structures.

[0345] 2-((4-(6-Benzyloxy-2-naphthyloxy)phenyl)carbonylamino)benzoic Acid Methyl Ester

[0346] Yield: 93%

[0347] 1 H-NMR (CDCl3); δ 3.95 (s, 3H), 5.20 (s, 2H), 7.00-7.15 (m, 2H), 7.20-7.30 (m, 4H), 7.35-7.45 (m, 4H), 7.49 (d, J=1.0 Hz, 2H), 7.50-7.60 (m, 1H), 7.60-7.70 (m, 1H), 7.76 (d, J=8.9 Hz, 11H), 8.04 (dd, J=2.0, 9.9 Hz, 2H), 8.10 (d, J=1.7 Hz, 1H), 8.90 (dd, J=1.0, 9.5 Hz, 1H), 12.0 (brs, 1H).

[0348] 2-((4-(4-Benzyloxyphenoxy)phenyl)carbonylamino)benzoic Acid Methyl Ester

[0349] Yield: 87%

[0350] 1 H-NMR (CDCl3); δ 12.00 (m, 1H), 8.91 (m, 1H), 8.02 (m, 3H), 7.61 (m, 1H), 6.98-7.45 (m, 12H), 5.08 (s, 2H), 3.97 (s, 3H).

[0351] 2-(2-(4-(4-Benzyloxyphenoxy)phenyl)acetylamino)benzoic Acid Methyl Ester

[0352] Yield: 75%

[0353] 1 H-NMR (CDCl3); δ 3.72 (2H, s), 3.87 (3H, s), 5.04 (2H, s), 6.91-7.02 (6H, m), 7.06 (1H, td, J=8.6, 1.6 Hz), 7.24-7.46 (7H, m), 7.52 (1H, td, J=8.0, 1.6 Hz), 7.99 (1H, dd, J=8.2, 1.6 Hz), 8.71 (1H, dd, J=8.6, 1.3 Hz), 11.03 (1H, brs).

Reference Example 23

[0354] Synthesis of 2-(2-(4-(6-hydroxy-2-naphthyloxy)phenyl)acetylamino)benzoic Acid Methyl Ester 1269

[0355] 2-((4-(6-Benzyloxy-2-naphthyloxy)phenyl)acetylamino)benzoic acid methyl ester (15.0 g, 29.0 mmol) obtained by the Reference Example 21 was dissolved in chloroform (150 ml) under heating and Pd-black (1.57 g) was added to the solution. The reaction system was stirred for a night at room temperature in hydrogen atmosphere. The reaction liquid was filtered with celite and the filtrate was concentrated. The residue was recrystallized from acetonitrile to obtain the subject compound (10.5 g, 24.5 mmol). The result of 1H-NMR was consistent with the above structure.

[0356] Light Brown Granular Crystal.

[0357] Yield: 92%

[0358] 1 H-NMR (CDCl3); δ 3.76 (s, 2H), 3.89 (s, 3H), 5.26 (brs, 1H), 7.02-7.15 (m, 5H), 7.22 (dd, J-2.3, 8.9 Hz, 1H), 7.31-7.37 (m, 3H), 7.53 (dt, J=1.7, 8.9 Hz, 1H), 7.60 (d, J=9.2 Hz, 1H), 7.64 (d, J=8.9 Hz, 1H), 8.01 (dd, J=1.7, 8.3 Hz, 1H), 8.72 (d, J=8.3 Hz, 1H), 11.10 (brs, 1H).

Reference Example 24

[0359] The following compounds were synthesized by a method similar to the Reference Example 23 using corresponding substrates. The results of 1H-NMR were consistent with the structures.

[0360] 2-((4-(6-Hydroxy-2-naphthyloxy)phenyl)carbonylamino)benzoic acid methyl Ester

[0361] Yield: 92%

[0362] 1 H-NMR (CDCl3); δ 3.88 (s, 3H), 5.26 (brs, 1H), 6.90-7.20 (m, 6H), 7.35 (brs, 1H), 7.50-7.70 (m, 3H), 7.90-8.05 (m, 3H), 8.84 (d, J=7.6 Hz, 1H), 11.95 (brs, 1H).

[0363] 2-((4-(4-Hydroxyphenoxy)phenyl)carbonylamino)benzoic Acid Methyl Ester

[0364] Yield: 93%

[0365] 1 H-NMR (DMSO-d6); δ 11.63 (brs, 1H), 9.57 (brs, 1H), 8.65 (d, 1H, J=8.25 Hz), 8.10 (dd, 1H, J=7.91, 1.32 Hz), 8.02 (d, 2H, J=8.58 Hz), 7.76 (dd, 1H, J=8.58, 7.26, 1.65 Hz), 7.32 (dd, 1H, J=7.92, 7.26, 0.99 Hz), 7.13 (d, 2H, J=8.91 Hz), 7.07 (d, 2H, J=8.91 Hz), 6.92 (d, 2H, J=8.91 Hz), 3.98 (s, 3H).

[0366] 2-(2-(4-(4-Hydroxyphenoxy)phenyl)acetylamino)benzoic Acid Methyl Ester

[0367] Yield: 66%

[0368] 1 H-NMR (DMSO-d6); δ 3.70 (2H, s), 3.78 (3H, s), 6.76 (2H, d, J=8.9 Hz), 6.88 (4H, d-like, J=8.6 Hz), 7.18 (1H, t, J=7.5 Hz), 7.30 (2H, d, J=8.6 Hz), 7.59 (1H, t, J=7.8 Hz), 7.89 (1H, dd, J=7.9, 1.7 Hz), 8.29 (1H, d, J=7.6 Hz), 9.31 (1H, s), 10.61 (1H, brs).

Example 1

[0369] The following compounds were synthesized by a method similar to the Reference Example 21 using corresponding substrates. The results of 1H-NMR were consistent with the structures.

[0370] 2-(2-(6-(4-Benzyloxyphenoxy)-3-pyridyl)acetylamino)benzoic Acid Methyl Ester (Compound No. 1078)

[0371] Yield: 36%

[0372] 1 H-NMR (CDCl3); δ 11.16 (brs, 1H), 8.68 (dd, 1H, J=0.66, 8.58 Hz), 8.16 (d, 1H, J=2.31 Hz), 7.99 (dd, 1H, J=1.65, 8.24 Hz), 7.70 (dd, 1H, J=2.31, 8.57 Hz), 7.53-729 (m, 6H), 7.09-6.96 (m, 6H), 6.87 (d, 1H, J=8.58 Hz), 5.03 (s, 2H), 3.86 (s, 3H), 3.68 (s, 2H).

[0373] 2-(2-(6-(6-Benzyloxy-2-naphthyloxy)-3-pyridyl)acetylamino)benzoic Acid Methyl Ester (Compound No. 1120)

[0374] Yield: 58%

[0375] 1 H-NMR (CDCl3); δ 3.72 (s, 2H), 3.91 (s, 3H), 5.18 (s, 2H), 6.96 (d, 1H, J=8.58 Hz), 7.06-7.77 (m, 14H), 8.02 (dd, 1H, J=1.65, 8.08 Hz), 8.18 (d, 1H, J=2.47 Hz), 8.70 (d, 1H, J=7.42 Hz), 11.19 (br, 1H).

[0376] 2-(2-(6-(4-(1-Ethylpropylthio)phenoxy)-3-pyridyl)acetylamino)benzoic acid Methyl ester (Compound No. 1093)

[0377] Yield: 69%

[0378] 1 H-NMR (CDCl3); δ 11.18 (brs, 1H), 8.69 (d, 1H, J=8.58 Hz), 8.19 (d, 1H, J=2.31 Hz), 8.01 (dd, 1H, J=1.65, 8.25 Hz), 7.75 (dd, 1H, J=2.64, 8.25 Hz), 7.53 (ddd, 1H, J=1.65, 7.26, 8.58 Hz), 7.42 (d, 2H, J=8.58 Hz), 7.07. (m, 3H), 6.93 (d, 1H, J=8.57 Hz), 3.89 (s, 3H), 3.72 (s, 2H), 2.91 (m, 1H), 1.60 (m, 4H), 1.01 (t, 6H, J=7.25 Hz).

[0379] 2-(2-(6-(2-Methyl-4-benzyloxyphenoxy)-3-pyridyl)acetylamino)benzoic acid Methyl ester (Compound No. 1094)

[0380] Yield: 21%

[0381] 1 H-NMR (CDCl3); δ 11.15 (brs, 1H), 8.69 (d, 1H, J=8.58 Hz), 8.14 (s, 1H, 7.98 (d, 1H, J=7.91 Hz), 7.69 (dd, 1H, J=2.31, 8.58 Hz), 7.51 (dd, 1H, J=7.58, 8.25 Hz), 7.44-7.31 (m, 5H), 7.06 (dd, 1H, J=7.58, 7.91 Hz), 6.98 (d, 1H, J=8.58 Hz), 6.88-6.79 (m, 3H), 5.03 (s, 2H), 3.86 (s, 3H), 3.68 (s, 21), 2.16 (s, 3H).

[0382] 2-(2-(6-(3-Methyl-4-benzyloxyphenoxy)-3-pyridyl)acetylamino)benzoic acid Methyl ester (Compound No. 1095)

[0383] Yield: 62%

[0384] 1 H-NMR (CDCl3); δ 11.18 (brs, 1H), 8.68 (d, 1H, J=8.24 Hz), 8.17 (d, 1H, J=2.31 Hz), 8.01 (dd, 1H, J=1.65, 8.24 Hz), 7.71 (dd, 1H, J=2.31, 8.24 Hz), 7.53 (ddd, 1H, J=1.65, 7.26, 8.90 Hz), 7.46-7.30 (m, 5H), 7.08 (ddd, 1H, J=0.99, 7.26, 8.24 Hz), 6.97-6.86 (m, 4H), 5.07 (s, 2H), 3.89 (s, 3H), 3.69 (s, 2H), 2.28 (s, 3H).

[0385] 2-(2-(6-(4-Benzyloxyphenylthio)-3-pyridyl)acetylamino)benzoic acid methyl Ester (Compound No. 1096)

[0386] Yield: 81%

[0387] 1 H-NMR (CDCl3); δ 11.17 (brs, 1H), 8.68 (d, 1H, J=8.58 Hz), 8.18 (d, 1H, J=2.31 Hz), 8.00 (dd, 1H, J=1.32, 7.92 Hz), 7.74 (dd, 1H, J=2.31, 8.58 Hz), 7.52 (ddd, 1H, J=1.32, 7.26, 8.58 Hz), 7.33-7.20 (m, 7H), 7.11-7.03 (m, 3H), 6.91 (d, 1H, J=8.25 Hz), 4.08 (s, 2H), 3.88 (s, 3H), 3.71 (s, 2H).

[0388] 2-((6-(4-Benzyloxyphenoxy)-3-pyridyl)carbonylamino)benzoic acid methyl Ester (Compound No. 1100)

[0389] Yield: 65%

[0390] 1 H-NMR (CDCl3); δ 12.08 (brs, 1H), 8.89 (s, 1H), 8.88 (d, 1H, J=6.6 Hz), 8.33 (dd, 1H, J=2.31, 8.58 Hz), 8.08 (dd, 1H, J=1.65, 7.92 Hz), 7.60 (t, 1H, J=7.26 Hz), 7.47-7.31 (m, 6H), 7.16-6.99 (m, 5H), 5.08 (s, 2H), 3.94 (s, 3H).

[0391] 4-Nitro-2-(2-(6-(4-benzyloxyphenoxy)-3-pyridyl)acetylamino)benzoic acid Methyl ester (Compound No. 1104)

[0392] Yield: 52% (in this case, coupled with 4-nitroanthranilic acid)

[0393] 1 H-NMR (CDCl3); δ 11.21 (brs, 1H), 9.60 (m, 1H), 8.17 (m, 2H), 7.88 (m, 1H), 7.71 (m, 1H), 7.43-7.25 (m, 5H), 7.10-6.89 (m, 5H), 5.06 (s, 2H), 3.96 (s, 3H), 3.74 (s, 2H).

[0394] 5-Chloro-2-(2-(6-(4-benzyloxyphenoxy)-3-pyridyl)acetylamino)benzoic acid Methyl ester (Compound No. 1110)

[0395] Yield: 72% (in this case, coupled with 5-chloroanthranilc acid)

[0396] 1 H-NMR (CDCl3); δ 11.05 (brs, 1H), 8.67 (d, 1H, J=8.91 Hz), 8.15 (d, 1H, J-2.64 Hz), 7.97 (d, 1H, J=2.64 Hz), 7.69 (dd, 1H, J=2.31, 8.57 Hz), 7.49-7.30 (m, 6H), 7.07 (d, 2H, J=8.90 Hz), 6.98 (d, 2H, J=9.24 Hz), 6.89 (d, 1H, 8.58 Hz), 5.05 (s, 2H), 3.89 (s, 3H), 3.69 (s, 2H).

[0397] 3-Methyl-2-(2-(6-(4-benzyloxyphenoxy)-3-pyridyl)acetylamino)benzoic Acid (Compound No. 1112)

[0398] Yield: 20% (in this case, coupled with 3-methylanthranilic acid)

[0399] 1 H-NMR (DMSO-d6); δ 11.94 (brs, 1H), 8.05 (s, 1H), 7.79 (d, 1H, J=8.58 Hz), 7.68 (d, 1H, J=7.25 Hz), 7.49-7.30 (m, 5H), 7.16 (d, 1H, J=7.59 Hz), 7.04 (s, 4H), 7.04 (m, 1H), 6.92 (d, 1H, J=8.24 Hz), 5.10 (s, 2H), 3.62 (s, 2H), 2.08 (s, 3H).

[0400] 2-(2-(N-Methyl-6-(4-benzyloxyphenoxy)-3-pyridyl)acetylamino)benzoic acid Methyl ester (Compound No. 1113)

[0401] Yield: 59%

[0402] 1 H-NMR (CDCl3); δ 8.02 (dd, 1H, J=1.65, 7.92 Hz), 7.65-7.55 (m, 2H), 7.51-7.30 (m, 7H), 7.22 (d, 1H, J=7.58 Hz), 7.04 (d, 2H, J=9.24 Hz), 6.97 (d, 2H, J=9.24 Hz), 6.77 (d, 1H, J=8.24 Hz), 5.05 (s, 2H), 3.83 (s, 3H), 3.25 (s, 2H), 3.20 (s, 3H).

[0403] 2-(2-(6-(6-Benzyloxy-2-naphthoxy)-3-pyridyl)acetylamino)benzoic acid Methyl ester (Compound No. 1206)

[0404] Yield: 58%

[0405] 1 H-NMR (CDCl3); δ 11.19 (br, 1H), 8.70 (d, 1H, J=7.42 Hz), 8.18 (d, 1H, J=2.47 Hz), 8.02 (dd, 1H, J=1.65, 8.08 Hz), 7.77-7.06 (m, 14H), 6.96 (d, 1H, J=8.58 Hz), 5.18 (s, 2H), 3.91 (s, 3H); 3.72 (s, 2H).

Example 2

[0406] The following compounds were synthesized by a method similar to the Reference Example 23 using corresponding substrates. The results of 1H-NMR were consistent with the structures.

[0407] 2-(2-(6-(4-Hydroxyphenoxy)-3-pyridyl)acetylamino)benzoic acid methyl Ester (Compound No. 1076)

[0408] Yield: 78%

[0409] 1 H-NMR (DMSO-d6); δ 10.63 (brs, 1H), 9.36 (brs, 1H), 8.20 (dd, 1H, J=0.99, 8.58 Hz), 8.08 (d, 1H, J=2.31 Hz), 7.89 (dd, 1H, J=1.32, 7.92 Hz), 7.78 (dd, 1H, J=2.31, 8.58 Hz), 7.59 (ddd, 1H, J=1.65, 6.93, 8.58 Hz), 7.19 (ddd, 1H, J=0.99, 6.93, 8.25 Hz), 6.94-6.89 (m, 3H), 6.77 (d, 2H, J=8.9 Hz), 3.79 (s, 3H), 3.74 (s, 2H).

[0410] 2-(2-(6-(6-Hydroxy-2-naphthyloxy)-3-pyridyl)acetylamino)benzoic acid Methyl ester (Compound No. 1204)

[0411] Yield: 82%

[0412] 1 H-NMR (CDCl3); δ 3.72 (s, 2H), 3.91 (s, 3H), 5.18 (brs, 1H), 6.97 (d, 1H, J=8.25 Hz), 7.07-8.18 (m, 11H), 8.69 (d, 1H, J=7.92 Hz).

[0413] 2-((6-(4-Hydroxyphenoxy)-3-pyridyl)carbonylamino)benzoic acid methyl Ester (Compound No. 1099)

[0414] Yield: 73%

[0415] 1 H-NMR (DMSO-d6); δ 11.41 (brs, 1H), 9.45 (brs, 1H), 8.69 (d, 1H, J=2.31 Hz), 8.41 (d, 1H, J=8.24 Hz), 8.29 (dd, 1H, J=2.64, 8.58 Hz), 7.98 (d, 1H, J=7.92 Hz), 7.67 (dd, 1H, J=7.25, 7.59 Hz), 7.25 (t, 1H, J=7.26 Hz), 7.11 (d, 1H, J=8.58 Hz), 7.00 (d, 2H, J=8.91 Hz), 6.80 (d, 2H, J=8.91 Hz), 3.86 (s, 3H).

Example 3

[0416] Synthesis of 2-(2-(6-(4-benzyloxyphenoxy)-3-pyridylacetylamino)benzoic Acid (Compound No. 986) 1270

[0417] 2-(2-(6-(4-Benzyloxyphenoxy)-3-pyridyl)acetylamino)benzoic acid methyl ester (87 mg, 0.186 mmol) obtained by the Example 1 was dissolved in a 2:1 mixed solvent (6 ml) of THF and methanol, 4N-lithium hydroxide (1 ml) was added thereto and the mixture was stirred for 1 hour at room temperature. After completing the reaction, the pH of the product was adjusted to about 4 with 10% aqueous solution of citric acid and the reaction product was extracted with ethyl acetate, washed with water, dried with magnesium sulfate and concentrated, and the residue was recrystallized from acetonitrile (20 ml) to obtain the subject compound (66 mg, 0.145 mmol). The result of 1H-NMR was consistent with the above structure.

[0418] Yield: 78%

[0419] 1 H-NMR (DMSO-d6); δ 13.56 (br, 1H), 11.18 (brs, 1H), 8.47 (d, 1H, J=8.25 Hz), 8.09 (d, 1H, J=1.98 Hz), 7.96 (dd, 1H, J-1.65, 7.92 Hz), 7.80 (d, 1H, J=8.58 Hz), 7.57 (t, 1H, J=7.92 Hz), 7.48-7.31 (m, 5H), 7.14 (t, 1H, J=7.59 Hz), 7.05 (s, 4H), 6.95 (d, 1H, J=8.25 Hz), 5.11 (s, 2H), 3.76 (s, 2H).

Example 4

[0420] The following compounds were synthesized by a method similar to the Example 3 using corresponding substrates.

[0421] 2-(2-(6-(4-(1-Ethylpropylthio)phenoxy)-3-pyridyl)acetylamino)benzoic Acid (Compound No. 1027)

[0422] Yield: 75%

[0423] 1 H-NMR (DMSO-d6); δ 13.55 (br, 1H), 11.18 (brs, 1H), 8.47 (d, 1H, J=8.25 Hz), 8.13 (s, 1H), 7.96 (d, 1H, J=7.91 Hz), 7.85 (d, 1H, J=8.58 Hz), 7.57 (t, 1H, J=7.92 Hz), 7.42 (d, 2H, J=8.58 Hz), 7.17-7.02 (m, 4H), 3.79 (s, 2H), 3.04 (m, 1H), 1.54 (m, 4H), 0.99 (t, 6H, J=7.26 Hz).

[0424] 2-(2-(6-(2-Methyl-4-benzyloxyphenoxy)-3-pyridyl)acetylamino)benzoic Acid (Compound No. 1039)

[0425] Yield: 83%

[0426] 1 H-NMR (DMSO-d6); δ 11.26 (brs, 1H), 8.45 (d, 1H, J=8.58 Hz), 8.04 (s, 1H), 7.95 (d, 1H, J=7.92 Hz), 7.78 (d, 1H, J=8.58 Hz), 7.56 (dd, 1H, J=7.26, 8.57 Hz), 7.48-7.31 (m, 5H), 7.13 (dd, 1H, J=7.26, 7.92 Hz), 6.98-6.83 (m, 4H), 5.09 (s, 2H), 3.74 (s, 2H), 2.05 (s, 3H).

[0427] 2-(2-(6-(3-Methyl-4-benzyloxyphenoxy)-3-pyridyl)acetylamino)benzoic Acid (Compound No. 1040)

[0428] Yield: 59%

[0429] 1 H-NMR (DMSO-d6); δ 13.70-13.40 (br, 1H), 11.24 (brs, 1H), 8.46 (d, 1H, J=8.25 Hz), 8.09 (d, 1H, J=2.31 Hz), 7.96 (d, 1H, J=7.92 Hz), 7.80 (dd, 1H, J=2.31, 8.25 Hz), 7.57 (dd, 1H, J=7.26, 8.58 Hz), 7.50-7.31 (m, 5H), 7.14 (dd, 1H, J=7.26, 7.92 Hz), 7.03 (d, 1H, J=8.58 Hz), 6.97-6.88 (m, 3H), 5.13 (s, 2H), 3.76 (s, 2H), 2.20 (s, 3H).

[0430] 2-(2-(6-(4-Benzyloxyphenylthio)-3-pyridyl)acetylamino)benzoic Acid (Compound No. 1053)

[0431] Yield: 91%

[0432] 1 H-NMR (DMSO-dc); δ 13.57 (br, 1H), 11.16 (brs, 1H), 8.46 (d, 1H, J=8.25 Hz), 8.12 (d, 1H, J=1.98 Hz), 7.95 (d, 1H, J=7.92 Hz), 7.84 (dd, 1H, J=2.31, 8.24 Hz), 7.57 (dd, 1H, J=7.26, 8.25 Hz), 7.38-7.21 (m, 7H), 7.14 (dd, 1H, J=7.26, 7.91 Hz), 7.06 (d, 2H, J=8.57 Hz), 7.01 (d, 1H, J=8.25 Hz), 4.22 (s, 2H), 3.78 (s, 2H).

[0433] 4-Nitro-2-(2-(6-(4-benzyloxyphenoxy)-3-pyridyl)acetylamino)benzoic Acid (Compound No. 1071)

[0434] Yield: 85%

[0435] 1 H-NMR (DMSO-d6); δ 11.28 (brs, 1H), 9.28 (s, 1H), 8.18 (d, 1H, J=8.91 Hz), 8.10 (s, 1H), 7.95 (d, 1H, J=8.91 Hz), 7.82 (d, 1H, J=8.58 Hz), 7.48-7.30 (m, 5H), 7.05 (s, 4H), 6.96 (d, 1H, J=8.58 Hz), 5.10 (s, 2H), 3.83 (s, 2H).

[0436] 5-Chloro-2-(2-(6-(4-benzyloxyphenoxy)-3-pyridyl)acetylamino)benzoic Acid (Compound No. 1111)

[0437] Yield: 72%

[0438] 1 H-NMR (DMSO-d6); δ 11.08 (brs, 1H), 8.47 (d, 1H, J=8.91 Hz), 8.08 (d, 1H, J=2.31 Hz), 7.89 (d, 1H, J=2.64 Hz), 7.80 (dd, 1H, J=1.98, 8.25 Hz), 7.64 (dd, 1H, J=2.31, 8.91 Hz), 7.48-7.31 (hi, 5H), 7.05 (s, 41), 6.95 (d, 1H, J=8.53 Hz), 5.11 (s, 2H), 3.77 (s, 2H).

[0439] 2-(2-(N-Methyl-6-(4-benzyloxyphenoxy)-3-pyridyl) acetylamino)benzoic acid (Compound No. 1114)

[0440] Yield: 54%

[0441] 1 H-NMR (DMSO-d6); δ 10.35 (br, 1H), 8.07 (d, 1H, J=1.65 Hz), 8.05 (dd, 1H, J=1.32, 8.25 Hz), 7.78 (dd, 1H, J=2.31, 8.58 Hz), 7.66 (dd, 1H, J=7.58, 7.92 Hz), 7.54-7.26 (m, 7H), 7.11 (d, 2H, J=9.24 Hz), 7.09 (d, 2H, J=9.56 Hz), 7.00 (d, 1H, J=8.58 Hz), 5.12 (s, 2H), 3.61 (s, 3H), 3.32 (s, 2H).

[0442] 2-(2-(6-(6-Benzyloxy-2-naphthoxy)-3-pyridyl)acetylamino)benzoic Acid (Compound No. 1120)

[0443] Yield: 97%

[0444] 1 H-NMR (CDCl3); δ 3.71 (s, 2H), 5.19 (s, 2H), 6.93 (d, 1H, J=8.41 Hz), 7.04-7.77 (m, 14H), 8.06 (dd, 1H, J=1.57, 8.00 Hz), 8.18 (d, 1H, J=2.31 Hz), 8.67 (d, 1H, J=9.24 Hz), 11.51 (br, 1H).

Example 5

[0445] Synthesis of 2-(2-(4-(6-(2-ethoxyethoxy)-2-naphthyloxy)phenyl)-acetylamino)benzoic Acid Methyl Ester (Methyl Ester of the Compound No. 1) 1271

[0446] 2 (2-(4-(6-Hydroxy-2-naphthyloxy)phenyl)acetylamino)benzoic acid methyl ester (214 mg, 0.50 mmol) obtained by the Reference Example 23 was dissolved in 5 ml of dry DMF under nitrogen atmosphere, potassium carbonate (104 mg, 0.75 mmol) was added to the solution and the mixture was stirred as it is for 1 hour. at room temperature. The reaction liquid was added with 2-ethoxyethyl bromide (84 mg, 0.55 mmol) and stirred for 3.5 hours at room temperature and for 4 hours at 80° C. The obtained reaction liquid was added with water and extracted twice with ethyl acetate. The organic layer was washed with saturated aqueous solution of sodium chloride and dried with anhydrous sodium sulfate, and the solvent was distilled out under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=6:1 to 5:1) to obtain the subject compound (199 mg, 0.398 mmol). The result of 1H-NMR was consistent with the above structure. Colorless oil.

[0447] Yield: 80%

[0448] 1 H-NMR (CDCl3); δ 1.27 (t, J=6.9 Hz, 3H), 3.64 (q, J=6.9 Hz, 2H), 3.75 (s, 2H), 3.84-3.88 (m, 2H), 3.88 (s, 3H), 4.24 (t, J=4.6 Hz, 2H), 7.02-7.25 (m, 6H), 7.31-7.37 (m, 3H), 7.50-7.57 (m, 1H), 7.60 (d, J=8.9 Hz, 1H), 7.69 (d, J=8.9 Hz, 1H), 8.01 (dd, J=1.7, 8.3 Hz, 111), 8.73 (dd, J=1.0, 8.6 Hz, 1H), 11.07 (br.s, 1H).

Example 6

[0449] The compounds described as the Example No. 6 in the Tables 44 to 72 and the methyl ester of the Compound No. 88 were synthesized by a method similar to the Example 5 using corresponding substrates. The compounds were identified by 1H-NMR and the data were consistent with the structures. These data are described in the Tables 44 to 72 and the Table 74. The Table 74 only describes the yield.

Example 7

[0450] Synthesis of 2-(2-(4-(6-(2-ethoxyethoxy)-2-naphthyloxy)phenyl)-acetylamino)benzoic Acid (Compound No. 1) 1272

[0451] 2-(2-(4-(6-(2-Ethoxyethoxy)-2-naphthyloxy)phenyl)acetylamino)-benzoic acid methyl ester (187 mg, 0.37 mmol) obtained by the Example 5 was dissolved in a mixed solvent composed of methanol/THF (3 nil/6 ml), 4N aqueous solution of lithium hydroxide (0.94 ml, 3.7 mmol) was added to the solution and the mixture was stirred at room temperature for a night. After completing the reaction, 5N hydrochloric acid was added to adjust the pH of the system to about 1 and the system was stirred for 0.5 hour at room temperature. Water was added to the reaction liquid and the product was extracted twice with ethyl acetate. The organic layer was washed with saturated aqueous solution of sodium chloride and dried with anhydrous sodium sulfate, and the solvent was distilled off. The residue was recrystallized from acetonitrile (1 ml) to obtain the subject compound (123 mg, 0.253 mmol). The result of 1H-NMR was consistent with the structure. Colorless plate crystal.

[0452] Yield: 68%

[0453] 1 H-NMR (DMSO-d6); δ 1.13 (t, J=6.9 Hz, 3H), 3.52 (q, J=6.9 Hz, 2H), 3.73-3.76 (m, 4H), 4.18 (t, J=4.3 Hz, 2H), 7.02 (d, J=8.6-Hz, 2H), 7.10-7.18 (m, 2H), 7.22-7.26 (m, 1H), 7.34-7.39 (m, 4H), −7.57 (t, J=8.9 Hz, 1H), 7.73 (d, J=8.9 Hz, 1H), 7.83 (d, J=8.9 Hz, 1H), 7.95 (dd, J=1.7, 7.9 Hz, 1H), 8.50.(d, J=8.3 Hz, 1H), 11.12 (brs, 1H), 13.57 (brs, 1H).

Example 8

[0454] The compounds described as the Example No. 8 in the Tables 44 to 72 and the compounds shown in the Table 74 were synthesized by a method similar to the Example 7 using corresponding substrates. The compounds were identified by 1H-NMR or LC-MS and the results were consistent with the above structures. These data are described in the Tables 44 to 72 and the Table 74.

Example 9

[0455] Synthesis of 2-(2-(4-(4-((2-furanyl)methoxy)phenoxy)phenyl)acetylamino)-benzoic Acid Methyl Ester (Methyl Ester of the Compound No. 428) 1273

[0456] Triphenylphosphine (216 mg, 0.83 mmol), 2-furanylmethanol (81 mg, 0.83 mmol) and 40% toluene solution of diethyl azodicarboxylate (360 mg, 0.83 mmol) were added to 2-(2-(4-(4-hydroxyphenoxy)phenyl)-acetylamino)benzoic acid methyl ester (100 mg, 0.28 mmol) obtained by the Reference Example 24 in nitrogen atmosphere and stirred for 2 hours at room temperature. After completing the reaction, the reaction liquid was concentrated and the obtained crude product was purified by silica gel column chromatography to obtain the subject compound (73 mg, 0.16 mmol). The result of

[0457] 1 H-NMR was consistent with the above structure. Yield: 57%

[0458] 1 H-NMR (CDCl3); δ 3.73 (2H, s), 3.87 (3H, s), 4.98 (2H, s), 6.37-6.43 (2H, m), 6.87-7.01 (6H, m), 7.07 (1H, t, J=7.0 Hz), 7.31 (2H, d, J=8.6 Hz), 7.45-7.56 (2H, m), 7.99 (1H, dd, J=7.9, 1.7 Hz), 8.71 (1H, d, J=8.3 Hz), 11.03 (1H, brs).

Example 10

[0459] The compounds described as the Example No.10 in the Tables 44 to 72 and the methyl esters of the compounds described in the Table 73 were synthesized by a method similar to the Example 9 using corresponding substrates. The compounds were identified by 1H-NMR and the results were consistent with the above structures. These data are shown in the Tables 44 to 72 and the Table 74. The Table 73 only describes the yield.

Example 11

[0460] The compounds described as the Example No. 11 in the Tables 44 to 72 and the compounds described in the Table 73 were synthesized by a method similar to the Example 7 using corresponding substrates obtained by the Examples 2, 9 and 10. The compounds were identified by 1H-NMR or LC-MS and the results were consistent with the above structures. These data are shown in the Tables 44 to 72 and the Table 73.

Example 12

[0461] Synthesis of 2-(2-(6-(4-benzyloxyphenylsulfinyl)-3-pyridyl)acetylamino)-benzoic Acid Methyl Ester (Compound No. 1097) 1274

[0462] 2-(2-(6-(4-Benzyloxyphenylthio)-3-pyridyl)acetylamino)benzoic acid methyl ester (62 mg, 0.128 mmol) obtained by the Example 1 was dissolved in a mixed solvent (5 ml) composed of methanol and methylene chloride (3:2) and the solution was cooled with ice. The solution was added with N-bromosuccinimde (45 mg, 0.256 mmol) and stirred for 1.5 hours under ice cooling. After completing the reaction, the reaction liquid was concentrated and purified by silica gel chromatography to obtain the subject compound (36 mg, 0.0719 mmol) as the objective product. The compound was identified by 1H-NMR and the result was consistent with the above structure.

[0463] Yield: 56%

[0464] 1 H-NMR (CDCl3); δ 11.21 (brs, 1H), 8.69 (d, 1H, J=8.25 Hz), 8.20 (d, 1H, J=2.31 Hz), 8.02 (dd, 1H, J=1.32, 8.25 Hz), 7.79 (dd, 1H, J=2.31, 8.58 Hz), 7.54 (ddd, 1H, J=1.32, 7.25, 8.58 Hz), 7.39 (d, 2H, J=8.90 Hz), 7.30-7.20 (n, 5H), 7.12-7.02 (m, 3H), 6.97 (d, 1H, J=8.92 Hz), 4.11 (d, 1H, J=15.22 Hz), 3.99 (d, 1H, J=12.54 Hz), 3.89 (s, 3H), 3.74 (s, 2H).

Example 13

[0465] Synthesis of 2-(2-(6-(4-benzyloxyphenylsulfinyl)-3-pyridyl)acetylamino)-benzoic Acid (Compound No. 1054) 1275

[0466] 2-(2-(6-(4-Benzyloxyphenylsulfinyl)-3-pyridyl)acetylamino)benzoic acid methyl ester (51 mg, 0.102 mmol) obtained by the Example 12 was dissolved in a mixed solvent (6 ml) composed of THF and methanol (2:1), added with 4N lithium hydroxide (1 ml) and stirred for 1 hour at room temperature. After completing the reaction, the pH of the reaction liquid was adjusted to about 7 using 1N aqueous solution of hydrochloric acid and a phosphate buffer solution, and the liquid was extracted with ethyl acetate, washed with water, dried with magnesium sulfate and concentrated. The residue was dissolved in a mixture of ethyl acetate and methanol (1:1) and hexane was added to the solution to precipitate a solid component and obtain the subject compound (35 mg, 0.0179 mmol) as the objective product. The compound was identified by 1H-NMR and the result was consistent with the above structure.

[0467] Yield: 70%

[0468] 1 H-NMR (DMSO-d6); δ 13.58 (br, 1H), 11.19 (brs, 1H), 8.47 (d, 1H, J=8.25 Hz), 8.18 (d, 1H, J=1.65 Hz), 7.96 (d, 1E, J=7.92 Hz), 7.90 (dd, 1H, J=2.31, 8.58 Hz), 7.57 (m, 3H), 7.25 (s, 5H), 7.17-7.07 (m, 4H), 4.27 (d, 1H, J=12.87 Hz), 4.10 (d, 1H, J=12.54 Hz), 3.81 (s, 2H).

Example 14

[0469] Synthesis of 2-(2-(1-hydroxy-6-(4-(1-ethylpropoxy)phenoxy)-3-pyridyl)acetylamino)benzoic acid (Compound No. 1246) 1276

[0470] 2-(2-(6-(4-(1-Ethylpropoxy)phenoxy)-3-pyridyl)acetylamino)benzoic acid (1.0 g, 2.30 mmol) obtained by the Example 11 was dissolved in a mixed solvent consisting of methylene chloride (30 ml) and methanol (10 ml) and m-chloroperbenzoic acid (50-60%, 0.99 g) was added to the solution in an ice bath. The reaction was continued as it is for 2 days, m-chloroperbenzoic acid (50-60%, 0.99 g) was added to the product in an ice bath and the reaction was continued for 2.5 hours. After completing the reaction, the system was added with excessive amount of saturated aqueous solution of sodium thiosulfate and stirred, the solvent was concentrated and the reaction product was extracted from the residue with methylene chloride. The organic solvent was washed with saturated aqueous solution of magnesium thiosulfate and water in the order, dried with anhydrous magnesium sulfate and concentrated. A small amount of ethyl acetate was added to the obtained residue to effect the dissolution of the residue, and hexane was added to the solution to precipitate a solid component and obtain the subject compound (0.18 g, 0.40 mmol) as the objective product. The compound was identified by 1H-NMR and the result was consistent with the above structure.

[0471] Yield: 17%

[0472] 1 H-NMR (DMSO-d6); δ 14.80-13.50 (br, 1H), 11.18 (brs, 1H), 8.45 (d, 1H, J=8.58 Hz), 8.39 (d, 1H, J=1.98 Hz), 7.97 (dd, 1H, J=1.65, 7.92 Hz), 7.58 (ddd, 1H, J=1.65, 7.26, 8.58 Hz), 7.33 (dd, 1H, J=1.98, 8.58 Hz), 7.16 (dd, 1H, J=7.26, 7.92 Hz), 7.10 (d, 1H, J=8.58 Hz), 6.96 (s, 4H), 4.16 (qui, 1H, J=5.94 Hz), 3.81 (s, 2H), 1.60 (dq, 4H, J=5.94, 7.59 Hz), 0.90 (t, 6H, J=7.59 Hz).

Example 15

[0473] Synthesis of 2-(2-(4-(4-(cis-4-(N,N-dibenzylamino)cyclohexyloxy)phenoxy)-phenyl)acetyl amino)benzoic Acid Methyl Ester 1277

[0474] 2-(2-(4-(4-Hydroxyphenoxy)phenyl)acetylamino)benzoic acid methyl ester (5.66 g, 15.0 mmol) obtained by the Reference Example 24 was dissolved together with trans-4-(N,N-dibenzylamino)cyclohexanol (8.73 g, 29.6 mmol) and PPh3 (7.87 g, 30.0 mmol) in N-methylmorpholine (90 ml) and cooled with ice. Azodicarboxylic acid diethyl ester (13.1 ml, 40% in PhMe, 30.0 mmol) was dropped into the solution spending 10 minutes. The mixture was stirred for a night at room temperature and the reaction liquid was concentrated. The obtained residue was purified by silica gel chromatography (hexane:ethyl acetate=20:1 to 7:1) to obtain the subject compound (7.03 g, 10.7 mmol). The 1H-NMR of the product was consistent with the above structure. Colorless foam.

[0475] Yield: 72%

[0476] 1 H-NMR (CDCl3); δ 1.3-1.5 (m, 2H), 1.6-1.8 (m, 2H), 1.8-1.9 (m, 2H), 2.0-2.2 (m, 2H), 2.5-2.7 (m, 1H), 3.68 (s, 4H), 3.72 (s, 2H), 3.87 (s, 3H), 4.39 (br, 1H), 6.86 (d, J=9.1 Hz, 2H), 6.95-6.98 (m, 4H), 7.06 (t, J=7.3 Hz, 1H), 7.17-7.23 (m, 2H), 7.26-7.32 (m, 6H), 7.37-7.40 (m, 4H), 7.52 (t, J=7.3 Hz, 1H), 7.99 (dd, J=1.8, 8.1 Hz, 1H), 8.72 (d, J=8.7 Hz, 1H), 11.03 (brs, 1H).

Example 16

[0477] The following compounds were synthesized by a method similar to the Example 15 using corresponding substrates. The results of 1H-NMR were consistent with the structures of respective compounds.

[0478] 2-(2-(4-(6-(cis-4-(N,N-Dibenzylamino)cyclohexyloxy)-2-naphthyloxy)-phenyl)acetylamino)benzoic Acid Methyl Ester

[0479] Yield: 81%

[0480] 1 H-NMR (CDCl3); δ 11.07 (brs, 1H), 8.72 (d, 1H, J=7.56 Hz), 8.00 (dd, 1H, J=8.10, 1.35 Hz), 7.68-7.49 (m, 2H), 7.40-7.02 (m, 20H), 4.59 (br, 11H), 3.88 (s, 3H), 3.74 (s, 2H), 3.69 (s, 4H), 2.61 (m, 1H), 2.21-2.16 (m, 2H), 2.04-1.69 (m, 4H), 1.50-1.42 (m, 2H)

[0481] 2-((4-(6-(cis-4-(N,N-Dibenzylamino)cyclohexyloxy)-2-naphthyloxy)phenyl)-carbonylamino)benzoic Acid Methyl Ester

[0482] Yield: 64%

[0483] 1 H-NMR (CDCl3); δ 12.00 (s, 1H), 8.92 (d, 1H, J=8.58 Hz), 806 (m, 2H), 7.66 (m, 2H), 7.09-7.41 (m, 19H), 4.62 (s, 1H), 3.95 (s, 3H), 3.71 (s, 4H), 2.62 (m, 1H), 2.21 (m, 2H), 1.89 (m, 2H), 1.73 (m, 2H), 1.45 (m, 2H).

[0484] 2-(2-(4-(7-(cis-4-(N,N-Dibenzylamino)cyclohexyloxy)-2-naphthyloxy)-phenyl)acetylamino)benzoic Acid Methyl Ester

[0485] Yield: 71%

[0486] 1 H-NMR (CDCl3); δ 11.10 (brs, 1H), 8.74 (d, 1H, J=8.25 Hz), 7.99 (dd, 1H, J=7.91, 1.32 Hz), 7.72-7.67 (m, 3H), 7.52 (dd, 1H, J=8.58, 7.25 Hz), 7.49-6.98 (m, 18H), 4.56 (br, 1H), 3.88 (s, 3H), 3.75 (s, 2H), 3.68 (s, 4H), 2.59 (m, 1H), 2.04 (m, 2H), 1.88-1.68 (m, 4H), 1.43 (m, 2H).

[0487] 2-((4-(4-(cis-4-(N,N-Dibenzylamino)cyclohexyloxy)phenoxy)phenyl)-carbonyl amino)benzoic Acid Methyl Ester

[0488] Yield: 93%

[0489] 1 H-NMR (CDCl3); δ 11.97 (brs, 1H), 8.91 (d, 1H, J=8.58 Hz), 8.07 (dd, 1H, J=7.75, 1.32 Hz), 8.00 (d, 2H, J=8.91 Hz), 7.59 (ddd, 1H, J=8.58, 7.09, 1.65 Hz), 7.40-6.90 (m, 17H), 4.43 (br, 1H), 3.95 (s, 3H), 3.69 (s, 4H), 2.60 (m, 1H), 2.11-1.23 (m, 8H).

[0490] 2-(2-(4-(4-(1-Benzylpiperidin-2-ylmethyloxy)phenyloxy)phenyl)-acetylamino)benzoic Acid Methyl Ester

[0491] Yield: 27%

[0492] 1 H-NMR (CDCl3); δ 11.03 (s, 1H), 8.71 (dd, 1H, J=8.4, 1.1 Hz), 7.98 (dd, 1H, J=8.1, 1.6 Hz), 7.52 (ddd, 1H, J=8.4, 7.3, 1.6 Hz), 7.23-7.37 (m, 7H), 7.06 (ddd, 1H, J=8.1, 7.3, 1.1 Hz), 6.92 (d, 2H, J=8.9 Hz), 6.82 (d, 2H, J=8.9 Hz), 6.55 (d, 2H, J=8.9 Hz), 3.86 (s, 3H), 3.72 (d, 1H, J=13.5 Hz), 3.72 (s, 2H), 3.59 (d, 1H, J=13.5 Hz), 2.89-2.99 (brm, 1H), 2.76-2.88 (brm, 1H), 2.60-2.68 (m, 2H), 2.04-2.13 (br, 1H), 1.67-1.78 (brm, 6H).

[0493] 2-(2-(4-(4-(1-Benzylpiperidin-3-ylmethyloxy)phenyloxyl)phenyl)-acetylamino)benzoic Acid Methyl Ester

[0494] Yield: 60%

[0495] 1 H-NMR (CDCl3); δ 11.03 (s, 1H), 8.71 (d, 1H, J=8.4 Hz), 7.99 (dd, 1H, J=8.1 Hz, 1.6 Hz), 7.52 (ddd, 1H, J=8.4 Hz, 7.3 Hz, 1.6 Hz), 7.24-7.32 (m, 7H), 7.06 (dd, 1H, J=8.1 Hz, 7.3 Hz), 6.93-6.98 (m, 4H), 6.82 (d, 2H, J=8.9 Hz), 3.87 (s, 3H), 3.72 (s, 2H), 3.56 (d, 1H, J=13.2 Hz), 3.48 (d, 1H, J=13.2 Hz), 2.14 (brm, 2H), 1.95-2.02 (m, 2H), 1.75-1.89 (m, 1H), 1.66-1.69 (brm, 6H).

[0496] 2-(2-(4-(4-(2-Dibenzylaminocyclohexyloxy)phenyloxy)phenyl)acetylamino)-benzoic Acid Methyl Ester

[0497] Yield: 13%

[0498] 1 H-NMR (CDCl3); δ 11.05 (s, 1H), 8.72 (d, 1H, J=8.6 Hz), 8.00 (dd, 1H, J=8.1 Hz, 1.6 Hz), 7.52 (ddd, 1H, J=8.6 Hz, 7.0 Hz, 1.6 Hz), 7.15-7.38 (m, 12H), 7.06 (dd, 1H, J=8.1 Hz, 7.0 Hz), 6.91-7.02 (m, 6H), 4.26 (brm, 1H), 3.87 (s, 3H), 3.81 (s, 2H), 3.73 (s, 2H), 3.69 (s, 2H), 2.83 (brm, 1H), 2.16 (br, 1H), 2.00 (br, 1H), 1.70 (brm, 2H), 1.61 (brs, 1H), 1.30-1.50 (brm, 1H), 1.18-1.26 (m, 2H).

Example 17

[0499] Synthesis of 2-(2-(4-(4-(cis-4-aminocyclohexyloxy)phenoxy)phenyl)-acetylamino)benzoic Acid Methyl Ester 1278

[0500] 2-(2-(4-(4-cis-4-(N,N-Dibenzylamino)cyclohexyloxyphenoxy)phenyl)-acetylamino)benzoic acid methyl ester (7.03 g, 10.74 mmol) obtained by the Example 15 was dissolved in a mixed solvent consisting of methanol (60 ml) and methylene chloride (60 ml), formic acid (5.3 ml, 0.14 mol) and Pd-Black (3.6 g) were added to the solution and the obtained mixture was stirred for 8 hours at room temperature. The reaction liquid was filtered with Celite and the filtrate was concentrated. The residue was dissolved in ethyl acetate and adjusted to pH>13 by the addition of concentrated ammonia water. The solution was extracted twice with ethyl acetate, and the organic layer was washed with saturated saline water, dried with anhydrous sodium sulfate and concentrated. The obtained residue was purified by silica gel column chromatography (hexane:ethyl acetate=2:1→simple ethyl acetate→chloroform:methanol:triethylamine=100:10:1) to obtain the subject compound (4.60 g, 9.69 mmol). The 1H-NMR of the product was consistent with the above structure. Pale yellow viscous liquid.

[0501] Yield: 90%

[0502] 1 H-NMR (CDCl3); δ 1.35 br, 2H), 1.5-1.7 (m, 6H), 1.95-2.15 (m, 2H), 2.78 (br, 1H), 3.72 (s, 2H), 3.88 (s, 3H), 4.39 (br, 1H), 6.85-6.89 (m, 2H), 6.95-6.98 (m, 4H), 7.06 (t, J=7.4 Hz, 1H), 7.31 (d, J=8.2 Hz, 2H), 7.52 (t, J=7.3 Hz, 1H), 7.99 (dd, J=1.7, 8.1 Hz, 1H), 8.71 (d, J=8.7 Hz, 1H), 11.03 (brs, 1H).

Example 18

[0503] The following compounds were synthesized by a method similar to the Example 17 using corresponding substrates. The results of 1H-NMR were consistent with the structures of respective compounds.

[0504] 2-((4-(4-(cis-4-Aminocyclohexyloxy)phenoxy)phenyl)carbonylamino)benzoic Acid Methyl Ester

[0505] Yield: 57%

[0506] 1 H-NMR (CDCl3); δ 11.98 (brs, 1H), 8.91 (d, 1H, J=8.37 Hz), 8.07 (d, 1H, J=7.83 Hz), 8.00 (d, 2H, J=8.64 Hz), 7.59 (dd, 1H, J=8.37, 7.56 Hz), 7.10 (dd, 1H, J=7.56, 7.29 Hz), 7.05-6.91 (m, 6H), 4.43 (br, 1H), 3.95 (s, 3H), 2.80 (br, 1H), 2.00 (m, 2H), 1.80-1.63 (m, 4H), 1.32 (m, 2H).

[0507] 2-(2-(4-(6-(cis-4-Aminocyclohexyloxy)-2-naphthyloxy)phenyl)acetylamino)-benzoic Acid Methyl Ester (Methyl Ester of the Compound No. 18)

[0508] Yield: 66%

[0509] 1 H-NMR (CDCl3); δ 11.07 (brs, 1H), 8.72 (d, 1H, J=8.41 Hz), 8.00 (dd, 1H, J=8.08, 1.65 Hz), 7.68-7.49 (m, 3H), 7.36-7.02 (m, 9H), 4.58 (br, 1H), 3.88 (s, 3H), 3.74 (s, 2H), 2.80 (m, 1H), 2.09-2.04 (m, 2H), 1.70-1.46 (m, 6H).

[0510] 2-((4-(6-(cis-4-Aminocyclohexyloxy)-2-naphthyloxy)phenyl)carbonylamino)benzoic Acid Methyl Ester

[0511] Yield: 99%

[0512] 1 H-NMR (CDCl3); δ 12.00 (s, 1H), 8.92 (d, 1H, J=8.58 Hz), 8.09 (m, 3H), 7.66 (m, 3H), 7.42 (s, 1H), 7.09-7.25 (m, 6H), 4.62 (s, 1H), 3.95 (s, 3H), 2.83 (m, 1H), 2.11 (m, 2H), 1.67 (m, 4H), 1.50 (br, 2H).

[0513] 2-(2-(4-(7-(cis-4-Aminocyclohexyloxy)-2-naphthyloxy)phenylacetylamino)-benzoic Acid Methyl Ester (Methyl Ester of the Compound No. 19)

[0514] Yield: 44%

[0515] 1 H-NMR (CDCl3); δ 11.10 (brs, 1H), 8.72 (d, 1H, J=8.58 Hz), 7.99 (dd, 1H, J=7.91, 1.65 Hz), 7.68-7.63 (m, 2H), 7.52 (dd, 1H, J=7.26, 6.92 Hz), 7.36 (d, 2H, J=8.58 Hz), 7.16-6.97 (m, 7H), 4.60 (br, 1H), 3.87 (s, 3H), 3.75 (s, 2H), 3.27 (m, 1H), 2.21-2.16 (m, 2H), 2.02 (m, 4H), 1.61 (m, 2H).

[0516] (R)-2-(2-(4-(4-(Pyrrolidin-2-ylmethyloxy)phenyloxy)phenyl)acetylamino)-benzoic Acid Methyl Ester

[0517] Yield: 32% (yield of two steps from the reaction similar to the Example 15)

[0518] 1 H-NMR (CDCl3); δ 11.04 (s, 1H), 8.71 (dd, 1H, J=8.6, 1.1 Hz), 7.99 (dd, 1H, J=8.1, 1.6 Hz), 7.52 (ddd, 1H, J=8.6, 7.3, 1.6 Hz), 7.30 (d, 2H, J=8.6 Hz), 7.06 (ddd, 1H, J=8.1, 7.3, 1.1 Hz), 6.85-6.99 (m, 6H), 4.11-4.18 (m, 1H), 4.04 (d, 1H, J=5.7 Hz), 3.88 (s, 3H), 3.72 (s, 2H), 3.09-3.41 (br, 1H), 3.12-3.19 (m, 2H), 2.89-2.94 (m, 1H), 1.75-2.08 (m, 4H).

[0519] 2-(2-(4-(4-(1-Aminocyclopentan-1-ylmethyloxy)phenyloxy)phenyl)-acetylamino)benzoic Acid Methyl Ester

[0520] Yield: 39% (yield of two steps from the reaction similar to the Example 15)

[0521] 1 H-NMR (CDCl3); δ 11.04 (s, 1H), 8.71 (d, 1H, J=8.4 Hz), 7.98 (dd, 1H, J=8.1 Hz, 1.6 Hz), 7.51 (ddd, 1H, J=8.4 Hz, 7.3 Hz, 1.6 Hz), 7.32 (d, 2H, J=8.6 Hz), 7.06 (dd, 1H, J=8.1 Hz, 7.3 Hz), 6.97 (d, 2H, J=8.6 Hz), 6.93 (s, 4H), 3.98-4.16 (br, 4H), 3.87 (s, 3H), 3.73 (s, 2H), 3.12 (s, 1H), 1.97-2.08 (brm, 2H), 1.63-1.73 (m, 6H).

[0522] (S)-2-(2-(4-(4-(Pyrrolidin-2-ylmethyloxy)phenyloxy)phenyl)acetylamino)-benzoic Acid Methyl Ester

[0523] Yield: 32% (yield of two steps from the reaction similar to the Example 15)

[0524] 1 H-NMR (CDCl3); δ 11.04 (s, 1H), 8.71 (dd, 1H, J=8.6, 1.1 Hz), 7.99 (dd, 1H, J=8.1, 1.6 Hz), 7.52 (ddd, 1H, J=8.6, 7.3, 1.6 Hz), 7.30 (d, 2H, J=8.6 Hz), 7.06 (ddd, 1H, J=8.1, 7.3, 1.1 Hz), 6.85-6.99 (m, 6H), 4.65-5.55 (br, 1H), 4.11-4.18 (m, 1H), 4.04 (d, 1H, J=5.7 Hz), 3.88 (s, 3H), 3.72 (s, 2H), 3.12-3.19 (m, 2H), 2.89-2.94 (m, 1H), 1.75-2.08 (m, 4H).

[0525] 2-(2-(4-(4-(Piperidin-2-ylmethyloxy)phenyloxy)phenyl)acetylamino)benzoic Acid Methyl Ester

[0526] Yield: 37%

[0527] 1 H-NMR (CDCl3); δ 11.04 (s, 1H), 8.71 (d, 1H, J=8.4 Hz), 7.99 (dd, 1H, J=8.1, 1.6 Hz), 7.51 (ddd, 1H, J=8.4, 7.3, 1.6 Hz), 7.31 (d, 2H, J=8.4 Hz), 7.06 (dd, 1H, J=8.1, 7.3 Hz), 6.91-6.97 (m, 6H), 5.20-5.75 (br, 1H), 3.87 (s, 3H), 3.72 (s, 2H), 3.35-3.42 (m, 2H), 3.23-3.33 (m, 2H), 1.69-2.04 (brm, 7H).

[0528] 2-(2-(4-(4-(Piperidin-3-ylmethyloxy)phenyloxy)phenyl)acetylamino)benzoic Acid Methyl Ester

[0529] Yield: 79%

[0530] 1 H-NMR (CDCl3); δ 11.04 (s, 1H), 8.71 (dd, 1H, J=8.4, 1.1 Hz), 7.99 (dd, 1H, J=7.8, 1.6 Hz), 7.52 (ddd, 1H, J=8.4, 7.3, 1.6 Hz), 7.30 (d, 2H, J=8.9 Hz), 7.06 (ddd, 1H, J=7.8, 7.3, 1.1 Hz), 6.97 (d, 2H, J=8.9 Hz), 6.95 (d, 2H, J=8.9 Hz), 6.83 (d, 2H, J=8.9 Hz), 3.88 (s, 3H), 3.72 (s, 2H), 3.86-3.75 (m, 2H), 3.38-3.41 (brm, 1H), 3.21-3.26 (brm, 1H), 2.61-2.76 (brm, 2H), 2.16-2.28 (br, 2H), 1.90-1.97 (brm, 1H), 1.82 (br, 2H).

[0531] 2-(2-(4-(4-(2-Aminocyclohexyloxy)phenyloxy)phenyl)acetylamino)benzoic Acid Methyl Ester

[0532] Yield: 58%

[0533] 1 H-NMR (CDCl3); δ 11.04 (s, 1H), 8.70 (dd, 1H, J=8.6, 1.1 Hz), 7.98 (dd, 1H, J=8.1, 1.6 Hz), 7.51 (ddd, 1H, J=8.6, 7.0, 1.6 Hz), 7.30 (d, 2H, J=8.6 Hz), 7.05 (ddd, 1H, J=8.1, 7.0, 1.1 Hz), 6.90-6.99 (m, 6H), 6.72 (br, 2H), 4.18 (brm, 1H), 3.86 (s, 3H), 3.71 (m, 2H), 2.95-3.01 (m, 1H), 2.17 (brm, 1H), 2.08 (brm, 1H), 1.71 (brm, 1H), 1.65 (brm, 1H), 1.33-1.43 (m, 2H), 1.21-1.26 (m, 2H).

Example 19

[0534] Compounds described in the Tables 48 and 49 as the Example No.19 and corresponding to respective starting raw materials were synthesized from 2-(2-(4-(6;-(cis-4-aminocyclohexyloxy)-2-naphthyloxy)-phenyl)acetylamino)benzoic acid methyl ester and 2-(2-(4-(7-(cis-4-aminocyclohexyloxy)-2-naphthyloxy)phenyl)acetylamino)benzoic acid methyl ester obtained by the Example 18 by the method similar to the Example 7. The yields and 1H-NMR data are shown in the Tables 48 and 49.

Example 20

[0535] Synthesis of 2-(2-(4-(6-(cis-4-(benzoylamino)cyclohexyloxy)-2-naphthyloxy)-phenyl)acetyl amino)benzoic Acid (compound No. 96) 1279

[0536] Step 1

[0537] A reactor was charged with 358 μl (1.7 eq, 179 μmol) of 0.5M triethylamine-chloroform solution containing 420 μl (105 μmol, 50 mg) of 2-(2-(4-(4-(cis-4-aminocyclohexyloxy)phenoxy)phenyl)acetylamino)benzoic acid methyl ester (0.25M-CHCl3) obtained by the Example 17, benzoyl chloride (1.5 eq, 22 mg) was added thereto and the mixture was stirred for 2.5 hours. After completing the reaction, 139 mg (157.5 μmol) of an aminomethylated polystyrene resin (product of Novabiochem) was added to the system and stirred for 12 hours. The solution was put on a Silica cartridge (product of Waters) and developed with a hexane/ethyl acetate mixture (½) and the obtained solution was distilled to remove the solvent.

[0538] Step 2

[0539] The compound obtained by the step 1 was dissolved in a mixture of tetrahydrofuran (1 ml) and methanol (0.5 ml), 4N lithium hydroxide solution (0.25 ml) was added thereto and the mixture was stirred over a night. After completing the reaction, the product was acidified with 6N-hydrochloric acid (0.25 ml), water (1 ml) was added, the obtained mixture was extracted with ethyl acetate (2 ml×3) and the organic layer was passed through a sodium sulfate cartridge (product of Waters). The solvent was distilled out and the residue was dried in a desiccator. The compound was identified from the molecular weight using LC-MS and the obtained molecular weight was consistent with the above structure. The data are described in the Table 76.

Example 21

[0540] The compounds described as the Example No.21 in the Tables 75 to 89 were synthesized by a method similar to the Example 20 using corresponding substrates. The compounds were identified by the molecular weight using LC-MS and the results were consistent with the structures. The results are shown in the Tables 75 to 89.

Example 22

[0541] Synthesis of 2-(2-(4-(4-(cis-4-(2-pyridylcarbonylamino)cyclohexyloxy)-phenoxy)phenyl)acetylamino)benzoic Acid (Compound No. 254) 1280

[0542] Step 1

[0543] 2-(2-(4-(4-(cis-4-Aminocyclohexyloxy)phenoxy)phenyl)acetylamino)benzoic acid methyl ester (47 mg, 0.1 mmol) obtained by the Example 17 was dissolved in preparatorily dried chloroform (0.5 ml) and the solution was added with HOBT (0.12 mmol, 16 mg) and picolinic acid (0.12 mmol, 15 mg). t-BuOH (0.4 ml) and chloroform (1.3 ml) were poured into the mixture, EDCl (0.12 mmol, 23 mg) was added thereto and the mixture was stirred over a night at room temperature. The obtained solution was put on a Silica cartridge (product of Waters) and developed with a mixture of hexane/ethyl acetate (1/2), and the obtained solution was distilled to remove the solvent.

[0544] Step 2

[0545] The compound obtained by the step 1 was dissolved in a mixture of tetrahydrofuran (1 ml) and methanol (0.5 ml), and the solution was added with 4N aqueous solution of lithium hydroxide (0.25 ml) and stirred over a night. After completing the reaction, the product was acidified with 6N hydrochloric acid (0.25 ml), added with water (1 ml) and extracted with ethyl acetate (2 ml×3), and the organic layer was passed through a sodium sulfate cartridge (product of Waters). The solvent was distilled off and the residue was dried in a desiccator. The obtained compound was identified by the molecular weight using LC-MS and the result was consistent with the above structure. The data are shown in the Table 83.

Example 23

[0546] The compounds described as the Example No.23 in the Tables 75 to 89 were synthesized by a method similar to the Example 22 using corresponding substrates. The compounds were identified by the molecular weight using LC-MS and the results were consistent with the above structures. The results are shown in the Tables 75 to 89.

Example 24

[0547] Synthesis of 2-(2-(4-(4-(N-acetyl-4-piperidyloxy)phenoxy)phenyl)-acetylamino)benzoic Acid (Compound No. 78) 1281

[0548] Step 1

[0549] A reactor was charged with 2-(2-(4-(4-(4-piperidyloxy)phenoxy)-phenyl)acetylamino)benzoic acid methyl ester (120 mg, 0.26 mmol), preparatorily dried dichloromethane was poured thereto, triethylamine (47 μl, 1.3 eq., 338 μmol) was charged to the reactor, subsequently acetyl chloride (24 μl, 1.3 eq., 338 μmol) was added thereto and the mixture was stirred for 2.5 hours. After completing the reaction, the reaction product was added with water, extracted with dichloromethane and dried with sodium sulfate, and the solvent was removed by distillation. The residue was purified by silica gel column chromatography.

[0550] Step 2

[0551] The compound produced by the step 1 was dissolved in the mixture of tetrahydrofuran (1 ml) and methanol (0.5 ml), mixed with 4N aqueous solution of lithium hydroxide (0.25 ml) and stirred over a night. After completing the reaction, the product was acidified with 6N hydrochloric acid (0.25 ml), extracted with ethyl acetate and dried with sodium sulfate. The solvent was distilled out and the residue was dried in a desiccator. The produced compound was identified by the molecular weight using LC-MS and the result was consistent with the above structure. The data are shown in the Table 76.

Example 25

[0552] The compounds described as the Example No.25 in the Tables 75 to 89 were synthesized by a method similar to the Example 24 using corresponding substrates. The compounds were identified by the molecular weight using LC-MS and the results were consistent with the structures. The results are shown in the Tables 75 to 89.

Example 26

[0553] The compound of the compound No. 17 was synthesized by using the compound No. 26 of the Table 1 by a method similar to the Referential Example 23. The compound was identified by 1H-NMR, and the results are shown in the Table 48.

Example 27

[0554] Synthesis of 2-(2-(4-(4-(t-butoxycarbonylmethoxy)phenoxy)phenyl)-acetylamino)benzoic Acid Methyl Ester 1282

[0555] Potassium carbonate (162 mg) was added to 221 mg of 2-(2-(4-(4-hydroxyphenyloxy)phenyl)acetylamino)benzoic acid methyl ester obtained by the Reference Example 24, the mixture was suspended in dried DMF (5 ml), t-butyl bromoacetate (130 μl) was added little by little to the suspension at room temperature, and the mixture was stirred as it is over a night at room temperature. After completing the reaction, DMF was distilled out under reduced pressure and the product was extracted with ethyl acetate. The organic layer was washed with saturated aqueous solution of potassium bisulfate and dried with anhydrous magnesium sulfate. After removing the solvent by distillation, the residue was purified by silica gel column chromatography (developing liquid: hexane:ethyl acetate 4:1 to 1:1) to obtain 174 mg of the subject compound. The 1H-NMR of the compound was consistent with the above structure.

[0556] Yield: 60%

[0557] 1 H-NMR (CDCl3); δ 11.04 (brs, 1H), 8.71 (dd, 1H, J=8.6, 1.0 Hz), 7.91 (dd, 1H, J=8.2 Hz, 1.7 Hz), 7.52 (ddd, 1H, J=8.6, 7.3, 1.7 Hz), 7.31 (d, 2H, J=8.6 Hz), 7.06 (ddd, 1H, J=8.2, 7.3, 1.0 Hz), 6.98 (d, 2H, J=9.2 Hz), 6.96 (d, 2H, J=8.6 Hz), 6.86 (d, 2H, J=9.2 Hz), 4.49 (s, 2H), 3.87 (s, 3H), 3.73 (s, 2H), 1.49 (s, 9H).

Example 28

[0558] Synthesis of 2-(2-(4-(4 (hydroxycarbonylmethoxy)phenoxy)phenyl)-acetylamino)benzoic Acid Methyl Ester 1283

[0559] TFA (4 ml) was added to 2-(2-(4-(4-(t-butoxycarbonylmethoxy)-phenoxy)phenyl)acetylamino)benzoic acid methyl ester produced by the Example 27 and the mixture was stirred for 2 hours at room temperature. After the reaction, TFA was distilled out under reduced pressure and the product was dissolved in ethyl acetate. The organic layer was washed with water and dried with anhydrous magnesium sulfate, and the solvent was distilled out under reduced pressure to quantitatively obtain the subject compound (164 mg). The result of 1H-NMR was consistent with the above structure.

[0560] Yield: 100%

[0561] 1 H-NMR (CDCl3); δ 11.09 (brs, 1H), 9.91 (brs, 1H), 8.68 (dd, 1H, J=8.6 Hz), 7.98 (dd, 1H, J=8.2, 1.7 Hz), 7.52 (ddd, 1H, J=8.6, 7.3, 1.7 Hz), 7.31.(d, 2H, J=8.6 Hz), 7.08 (dd, 1H, J=8.2, 7.3 Hz), 6.99 (d, 2H, J=9.2 Hz), 6.96 (d, 2H, J-8.6 Hz), 6.89 (d, 2H, J=9.2 Hz), 4.65 (s, 2H), 3.86 (s, 3H), 3.76 (s, 2H).

Example 29

[0562] Synthesis of 2-(2-(4-(4-(piperidinamidomethyloxy)phenoxy)phenyl)-acetylamino)benzoic Acid Methyl Ester (Methyl Ester of the Compound No. 42) 1284

[0563] 2-(2-(4-(4-(Hydroxycarbonylmethoxy)phenoxy)phenyl)acetylamino)benzoic acid methyl ester (164 mg, 0.377 mmol) obtained by the Example 28 was suspended in methylene chloride (10 ml) and oxalyl chloride (34 μl) was added to the suspension at room temperature. The product was changed to transparent brown color under foaming by the addition of about 2 drops of dried DMF. After stirring at room temperature for 2 hours, the solvent and excess oxalyl chloride were distilled off under reduced pressure, and the residue was dissolved in methylene chloride (10 ml). Piperidine (35 μl) and triethylamine (54 μl) were added to the solution and reacted over a night at room temperature. The product was extracted with methylene chloride, and the organic layer was washed with saturated aqueous solution of potassium bisulfate and dried with anhydrous magnesium sulfate. The product was subjected to silica gel column chromatography (developing liquid; hexane:ethyl acetate=1:1) to obtain the subject compound (118 mg, 0.234 mg). The result of 1H-NMR was consistent with the above structure.

[0564] Yield: 62%

[0565] 1 H-NMR (CDCl3); δ 11.04 (brs, 1H), 8.71 (dd, 1H, J=8.6 Hz, 1.0 Hz), 7.99 (dd, 1H, J=7.9 Hz, 1.7 Hz), 7.52 (ddd, 1H, J=8.6, 7.3, 1.7 Hz), 7.31 (dd, 2H, J=8.6, 2.0 Hz), 7.06 (ddd, 1H, J=7.9, 7.3, 1.0 Hz), 6.98 (d, 2H, J=9.2, 2.6 Hz), 6.96 (dd, 2H, J=9.2, 2.6 Hz), 6.92 (dd, 2H, J=8.6, 2.0 Hz), 4.66 (s, 2H), 3.87 (S, 3H), 3.72 (S, 2H), 3.55-3.58 (br, 2H), 3.46-3.50 (br, 2H), 1.57-1.68 (br, 6H).

Example 30

[0566] The compound of the compound No. 42 of the Table 2 was synthesized by a method similar to the Example 7 using the compound obtained by the Example 29. The result of 1H-NMR was consistent with the above structure. The data are shown in the Table 55.

Example 31

[0567] Synthesis of 2-(2-(4-(4-(3-(tert-butoxycarbonylamino)benzyloxy)phenoxy)-phenyl)acetylamino)benzoic Acid Methyl Ester 1285

[0568] 2-(2-(4-(4-Hydroxyphenoxy)phenyl)acetylamino)benzoic acid methyl ester obtained by the Reference Example 24 (315 mg, 0.83 mmol) was dissolved in 20 ml of methylene chloride-THF mixture (1:1 v/v), added with 3-(tert-butoxycarbonylamino)benzyl alcohol (465 mg, 2.1 mmol), 1,1′-azobis(N,N′-dimethylformamide) (359 mg, 2.08 mmol) and tri-n-butyl phosphine (520 ml, 2.1 mmol) and the reaction mixture was stirred over a night. After completing the reaction, the solvent was removed under reduced pressure and the obtained crude residue was purified by silica gel chromatography (elution solvent; hexane:ethyl acetate 75:25 v/v) to obtain the subject compound (404 mg, 0.693 mmol) in the form of a colorless gummy substance. The result of 1H-NMR was consistent with the above structure.

[0569] Yield: 83%

[0570] 1 H-NMR (CDCl3); δ 11.03 (brs, 1H), 8.72 (dd, 1H, J=1.08, 8.64 Hz), 7.99 (dd, 1H, J=1.89, 8.10 Hz), 7.55-7.49 (m, 2H), 7.34-7.26 (m, 6H), 7.04-6.90 (m, 6H), 7.51 (brs, 1H), 5.02 (s, 2H), 3.87 (s, 3H), 3.73 (s, 2H), 1.52 (s, 9H).

Example 32

[0571] The following compound was synthesized by a method similar to the Example 31 using the corresponding substrate. The result of 1H-NMR was consistent with the structure.

[0572] 2-(2-(4-(4-(4-(tert-Butoxycarbonylamino)benzyloxy)phenoxy)phenyl)-acetylamino)benzoic Acid Methyl Ester

[0573] Yield: 46%

[0574] 1 H-NMR (CDCl3); δ 11.03 (brs, 1H), 8.71 (d, 1H, J=7.56 Hz), 7.99 (dd, 1H, J=1.62, 7.83 Hz), 7.51 (dt, 1H, J=1.35, 8.64 Hz), 7.34-7.30 (m, 4H), 7.28-7.25 (m, 2H), 7.07 (t, 1H, J=8.37 Hz), 7.00-6.90 (m, 6H), 6.49 (s, 1H), 4.98 (s, 2H), 3.87 (s, 3H), 3.72 (s, 2H), 1.52 (s, 9H).

Example 33

[0575] Synthesis of 2-(2-(4-(4-(2-(tert-butoxycarbonylamino)benzyloxy)phenoxy)-phenyl)acetylamino)benzoic Acid Methyl Ester 1286

[0576] 2-(2(4-(4-Hydroxyphenoxy)phenyl)acetylamino)benzoic acid methyl ester (300 mg, 0.82 mmol) obtained by the Reference Example 24 was dissolved in anhydrous N-dimethylformamide (10 ml), added with sodium hydride (30 mg, abt. 60%), stirred for 15 minutes and added with N-tert-butoxycarbonyl-2-bromomethylaniline (540 mg, 1.9 mmol). The reaction mixture was stirred over a night at room temperature, water (150 ml) was added thereto, the mixture was extracted with ethyl acetate (50 ml×2) and washed with water (100 ml×3), the organic solvent was dried with anhydrous magnesium sulfate and the solvent was removed under reduced pressure. The obtained residue was purified by silica gel chromatography (elution solvent; hexane:ethyl acetate 75:25 v/v) to obtain the subject compound (234 mg, 0.402 mmol) in the form of a colorless gummy substance. The result of 1H-NMR was consistent with the above structure.

[0577] Yield: 49%

[0578] 1 H-NMR (CDCl3); δ 11.05 (brs, 1H), 8.72 (dd, 1H, J=1.03, 8.37 Hz), 7.99 (dd, 1H, J=1.62, 8.10 Hz), 7.93 (d, 1H, J=8.37 Hz), 7.52 (dt, 1H, J=1.62, 7.29 Hz), 7.42-7.25 (m, 6H), 7.09-6.94 (m, 7H), 5.05 (s, 2H), 3.89 (s, 3H), 3.73 (s, 2H), 1.51 (s, 9H).

Example 34

[0579] Synthesis of 2-(2-(4-(4-(3-(acetylamino)benzyloxy)phenoxy)phenyl)-acetylamino)benzoic Acid Methyl Ester (Methyl Ester of the Compound No. 50) 1287

[0580] 2-(2-(4-(4-(3-(tert-Butoxycarbonylamino)benzyloxy)phenoxy)-phenyl)acetylamino)benzoic acid methyl ester (155 mg, 0.266 mmol) obtained by the Example 31 was dissolved in 4N hydrochloric acid-1,4-dioxane solution (5.0 ml) and stirred for 30 minutes at room temperature. The solvent was quickly removed under reduced pressure and the residue was dried under reduced pressure. The dried residue was dissolved in methylene chloride (10 ml) and triethylamine (0.11 ml, 0.789 mmol), added with acetyl chloride (0.025 ml) and stirred for a night at room temperature. After completing the reaction, the reaction liquid was added with water (100 ml) and immediately extracted with ethyl acetate (20 ml X 2). The collected ethyl acetate layer was dried with anhydrous magnesium sulfate and filtered, and the solvent was removed under reduced pressure. The obtained residue was purified by silica gel chromatography (elution, hexane:ethyl acetate 6:4 v/v) to obtain the subject compound (110 mg, 0.215 mmol) in the form of a colorless gummy substance. The result of 1H-NMR was consistent with the above structure.

[0581] Yield: 81%

[0582] 1 H-NMR (CDCl3); δ 11.04 (brs, 1H), 8.71 (d, 1H, J=8.37 Hz), 7.99 (dd, 1H, J=1.62, 8.10 Hz), 7.60 (brs, 1H), 7.53 (dd, 2H, J=1.62, 8.64 Hz), 7.45-7.23 (m, 4H), 7.17 (d, 1H, J=7.56 Hz), 7.06 (t, 1H, J=7.02 Hz), 7.00-8.89 (m, 6H), 5.02 (s, 2H), 3.87 (s, 3H), 3.72 (s, 2H), 2.17 (s, 3H).

Example 35

[0583] The following compounds were synthesized by a method similar to the Example 34 using the compounds obtained by the Examples 32 and 33 and reacting with respective corresponding substrates. The results of 1H-NMR were consistent with the structures.

[0584] 2-(2-(4-(4-(3-(Benzoylamino)benzyloxy)phenoxy)phenyl)acetylamino)benzoic Acid Methyl Ester (Methyl Ester of the Compound No. 51)

[0585] Yield: 49%

[0586] 1 H-NMR (CDCl3); δ 11.03 (brs, 1H), 8.70 (d, 1H, J=8.37 Hz), 8.16 (brs, 1H), 7.99 (dd, 1H, J=1.62, 8.10 Hz), 7.88 (dd, 2H, J=1.62, 6.76 Hz), 7.78 (brs, 1H), 7.64 (d, 1H, J=7.56 Hz), 7.55-7.20 (m, 9H), 7.09-6.91 (m, 6H), 5.05 (s, 2H), 3.86 (s, 3H).

[0587] 2-(2-(4-(4-(2-(Acetylamino)benzyloxy)phenoxy)phenyl)acetylamino)benzoic Acid Methyl Ester (Methyl Ester of the Compound No. 46)

[0588] Yield: 68%

[0589] 1 H-NMR (CDCl3); δ 11.06 (brs, 1H), 8.71 (d, 1H, J=8.64 Hz), 8.14 (brs, 1H), 8.07 (d, 1H, J=8.37 Hz), 8.00 (dd, 1H, J=1.62, 8.10 Hz), 7.54 (dt, 1H, J=1.62, 8.91 Hz), 7.38-7.26 (m, 5H), 7.16-7.93 (m, 7H), 5.06 (s, 2H), 3.87 (s, 3H), 3.73 (s, 2H), 2.13 (s, 3H).

[0590] 2-(2-(4-(4-(2-(Methoxycarbonylamino)benzyloxy)phenoxy)phenyl)-acetylamino)benzoic Acid Methyl Ester (Methyl Ester of the compound No. 48)

[0591] Yield: 80%

[0592] 1 H-NMR (CDCl3); δ 11.04 (brs, 1H), 8.72 (d, 1H, J=8.73 Hz), 8.00 (d, 1H, J=8.10 Hz), 7.52 (t, 1H, J=8.00 Hz), 7.40-7.90 (m, 13H), 6.78-6.60 (m, 1H), 5.00 (s, 2H), 3.86 (s, 3H), 3.73 (s, 2H), 3.59 (s, 3H).

[0593] 2-(2-(4-(4-(2-(Benzoylamino)benzyloxy)phenoxy)phenyl)acetylamino)benzoic Acid Methyl Ester (Methyl Ester of the Compound No. 49)

[0594] Yield: 63%

[0595] 1 H-NMR (CDCl3); δ 11.06 (brs, 1H), 9.16 (brs, 1H), 8.73 (d, 1H, J=8.37 Hz), 8.33 (d, 1H, J=8.37 Hz), 8.11 (d, 1H, J=7.12 Hz), 8.00 (dd, 2H, J=1.89, 6.21 Hz), 7.88-7.60 (m, 4H), 7.60-7.15 (m, 7H), 7.10-6.91 (m, 5H), 5.16 (s, It 2H), 3.86 (s, 3H), 3.73 (s, 2H).

Example 36

[0596] The compounds described in the Table 90 as example No.36 were synthesized by a method similar to the Example 7 using the corresponding substrates obtained by the Examples 34 and 35. The produced compounds were confirmed by LC-MS and the results were consistent with the structures. The results are shown in the Table 90.

Example 37

[0597] Synthesis of 2-((4-(6-(3-aminopropoxy)-2-naphthyloxy)phenyl)-carbonylamino)benzoic Acid (Compound No. 33) 1288

[0598] 2-((4-(6-(3-(tert-Butoxycarbonylamino)propoxy)-2-naphthyloxy)-phenyl)carbonylamino)benzoic acid (compound No. 31, 50 mg, 0.09 mmol) obtained by the Example 8 was dissolved in 3 ml of 4N hydrochloric acid-1,4-dioxane solution and 2.5 ml of 1,4-dioxane, stirred at room temperature for 5.5 hours and at 50 to 60° C. for 7 hours (3 ml of 4N hydrochloric acid-1,4-dioxane solution was added 3 hours after heating) and further stirred at room temperature for a night. After completing the reaction, the reaction liquid was concentrated and the crude product was recrystallized from ethanol (4 ml) to obtain the subject compound (14.5 mg, 0.0317 mmol) in the form of white granular crystal. The result of 1H-NMR was consistent with the structure.

[0599] Yield: 35%

[0600] 1 H-NMR (DMSO-d6); δ 2.07 (quint, J=5.9 Hz, 2H), 2.95-3.10 (m, 2H), 4.18 (t, J=5.9 Hz, 2H), 7.15-7.23 (m, 4H), 7.33 (dd, J=2.3, 8.9 Hz, 1H), 7.38 (d, J=2.0 Hz, 1H), 7.57 (d, J=2.6 Hz, 1H), 7.61-7.64 (m, 1H), 7.82 (d, J=8.9 Hz, 1H), 7.91 (d, J=9.2 Hz, 1H), 7.98 (d, J=8.9 Hz, 2H), 8.04 (d, J=8.3 Hz, 1H), 8.69 (d, J=8.6 Hz, 1H).

TABLE 44
Compound	Yield		Example
No.	(%)	1H-NMR(CDCl3): δ	No.
1	68	1H-NMR (DMSO-d6); δ 1.13(t, J=6.9Hz, 3H), 3.52(q,	7
		J=6.9Hz, 2H), 3.73-3.76(m, 4H), 4.18(t, J=4.3, 2H),
		7.02(d, J=8.6Hz, 2H), 7.10-7.18(m, 2H), 7.22-7.26(m,
		1H), 7.34-7.39(m, 4H), 7.57(t, J=8.9Hz, 1H), 7.73(d,
		J=8.9Hz, 1H), 7.83(d, J=8.9Hz, 1H), 7.95(dd, J=1.7, 7.9Hz,
		1H), 8.50(d, J=8.3Hz, 1H), 11.12(br.s, 1H),
		13.57(br.s, 1H).
1	80	1.27(t, J=6.9Hz, 3H), 3.64(q, J=6.9Hz, 2H), 3.75(s, 2H),	5
methyl		3.84-3.88(m, 2H), 3.88(s, 3H), 4.24(t, J=4.6Hz, 2H),
ester		7.02-7.25(m, 6H), 7.31-7.37(m, 3H), 7.50-7.57(m, 1H),
		7.60(d, J=8.9Hz, 1H), 7.69(d, J=8.9Hz, 1H), 8.01(dd,
		J=1.7, 8.3Hz, 1H), 8.73(dd, J=1.0, 8.6Hz, 1H),
		11.07(br.s, 1H).
2	73	1H-NMR (DMSO-d6); δ 1.91(quint, J=6.3Hz, 2H),	8
		3.20(q, J=6.3Hz, 2H), 3.75(s, 2H), 4.08(t, J=6.3Hz, 2H),
		5.01(s, 2H), 7.02(d, J=8.6Hz, 2H), 7.07-7.16(m, 2H),
		7.23-7.39(m, 10H), 7.57(t, J=8.6Hz, 1H), 7.72(d, J=8.9Hz,
		1H), 7.83(d, J=8.9Hz, 1H), 7.95(dd, J=1.7, 7.9Hz,
		1H), 8.50(d, J=8.3Hz, 1H), 11.13(br.s, 1H), 13.57(br.s,
		1H).
2	69	11.08(brs, 1H), 8.72(t, 1H, J=8.3, 1.3Hz), 8.01(dd, 1H,	6
methyl		J=8.3, 1.3Hz), 7.69(d, 1H, J=8.9Hz), 7.60(d, 1H, J=9.6Hz),
ester		7.53(t, 1H, J=8.3Hz), 7.37-7.31(m, 8H),
		7.25-7.22(m, 1H), 7.12-7.03(m, 5H), 5.11(s, 2H), 4.14(t,
		2H, J=6.9Hz), 3.89(s, 3H), 3.75(s, 2H), 3.48(q, 2H, J=6.6Hz),
		2.10-2.05(m, 2H).
3	69	1H-NMR (DMSO-d6); δ 1.35-1.65(m, 4H), 1.77(quint,	8
		J=6.6Hz, 2H), 2.24(t, J=7.3Hz, 2H), 3.74 (s, 2H), 4.05(t,
		J=6.6Hz, 2H), 7.02(d, J=8.6Hz, 2H), 7.10-7.15(m, 2H),
		7.23(dd, J=2.6, 8.9Hz, 1H), 7.32-7.38(m, 4H), 7.56(t,
		J=8.6Hz, 1H), 7.72(d, J=9.2Hz, 1H), 7.83(d, J=9.2Hz,
		1H), 7.95(dd, J=1.7, 7.9Hz, 1H), 8.50(d, J=7.6Hz, 1H),
		11.28(br.s, 1H).
3	100	11.07(brs, 1H), 8.73(dd, 1H, J=8.6, 1.0Hz), 8.01(dd, 1H,	6
methyl		J=7.9, 1.7Hz), 7.69(d, 1H, J=8.9Hz), 7.60(d, 1H, J=9.6Hz),
ester		7.57-7.50(m, 1H), 7.37-7.31(m, 3H), 7.23(dd, 1H,
		J=8.9, 2.6Hz), 7.15-7.02(m, 5H), 4.14(q, 2H, J=7.3Hz),
		4.07(t, 2H, J=6.6Hz), 3.88(s, 3H), 3.75(s, 2H), 2.35(t, 2H,
		J=7.3Hz), 1.95-1.80(m, 2H), 1.80-1.65(m, 2H),
		1.65-1.45(m, 2H), 1.26(t, 3H, J=7.3Hz).

[0601]

TABLE 45
4	53	1 H-NMR(DMSO-d6); δ 13.57(brs, 2H),	8
		11.17(s, 1H), 11.13(s, 1H), 8.51(d, 1H, J = 3.3 Hz),
		8.48(d, 1H, J = 3.3 Hz), 7.98-7.93(m, 2H), 7.82
		(d, 1H, J = 8.9 Hz), 7.72(d, 1H, J = 9.2 Hz),
		7.61-7.54(m, 2H), 7.38-7.33(m, 4H), 7.23(dd,
		1H, J = 8.9, 2.6 Hz), 7.16-7.11(m, 3H),
		7.02(d, 2H, J = 8.6 Hz), 4.14(t, 2H, J = 6.3 Hz),
		3.75(s, 2H), 2.61(t, 2H, J = 6.9 Hz), 2.12(qint,
		2H, J = 6.9 Hz).
4	41	11.05(brs, 1H), 11.08(brs, 1H), 8.74(dd, 1H, J = 8.6,	6
methyl		1.0 Hz), 8.73(dd, 1H, J = 8.3, 1.0 Hz), 8.01
ester		7.67(d, 1H, J = 8.9 Hz), 7.60-7.50(m, 3H),
methyl		4.18(t, 2H, 7.38-7.31(m, 3H), 7.22(dd, 1H,
ester		J = 8.9, 2.6 Hz),7.15-7.02(m, 6H),
		4.18(t, 2H, J = 6.3 Hz), 3.88(s, 3H),
		3.87(s, 3H), 3.75(s,2H), 2.71(t, 2H, J = 6.9 Hz),
		2.30 (quint, 2H, J = 6.9 Hz).
5	86	1 H-NMR(DMSO-d6); δ 1.91(quint, J = 6.3 Hz, 2H),	8
		3.59(t, J = 6.3 Hz, 2H), 3.75(s, 2H), 4.13
		(t, J = 6.3 Hz, 2H), 5.16(br.s, 1H), 7.02
		(d, J = 8.6 Hz, 2H), 7.10-7.16(m, 2H), 7.24
		(dd, J = 2.6, 8.6 Hz, 1H), 7.33-7.39 (m, 4H), 7.57(t,
		J = 8.9 Hz, 1H), 7.72(d, J = 8.9 Hz, 1H), 7.84
		(d, J = 9.2 Hz, 1H), 7.95(dd, J = 1.3, 8.3 Hz, 1H),
		8.49(d, J = 8.6 Hz, 1H), 11.72(s, 1H), 14.17(br.s, 1H).
5	44	11.08(brs, 1H), 8.73(dd, 1H, J = 8.6, 1.3 Hz), 8.01	6
methyl		(dd, 1H, J = 8.2, 1.7 Hz), 7.70(d, 1H, J = 8.9 Hz),
ester		7.61(d, 1H, J = 8.6 Hz), 7.53(t, 1H, J = 8.6 Hz), 7.37-
		7.32(m, 3H), 7.25-7.22(m, 1H), 7.15-7.03(m, 5H),
		4.24 (t, 2H, J =]5.9 Hz), 3.99-3.87(m, 5H), 3.75
		(s, 2H), 2.12(quint, 2H, J = 5.9 Hz).
6	50	1 H-NMR(DMSO-d6); δ 3.72(s, 2H), 5.68(s, 2H),	8
		7.02(s,J = 8.6 Hz, 2H), 7.08(t, J = 7.5 Hz, 1H),
		7.21-7.27(m, 2H), 7.36-7.39(m, 4H), 7.49
		(t, J = 6.9 Hz, 1H), 7.56-7.61(m, 2H), 7.68-7.81
		(m, 3H), 7.96(dd, J = 7.9, 1.5 Hz, 1H), 8.07
		(d, J = 8.0 Hz, 2H), 8.50(d, J = 8.0 Hz, 1H),
		11.91(brs, 1H).
6	95	11.08(brs, 1H), 8.72(d, 1H, J = 8.0 Hz), 8.06-7.98	6
methyl		(m, 3H), 69-7.61(m, 3H), 7.55-7.49(m, 3H),
ester		7.37-7.32(m, 7.26-7.21(m, 2H), 7.13-7.05(m, 4H),
		5.38 (s, 2H), 3.88(s, 3H) 3.75(s, 2H).

[0602]

TABLE 46
7	63	Hydrochloride: 1H-NMR (DMSO-d6); δ 3.18(4H, brs),	8
		3.43(2H, s br), 3.76(2H, s), 3.83(4H, t-like, J=4.6Hz),
		4.45(2H, t-like, J=5.0Hz), 7.03(2H, d, J=8.6Hz),
		7.14(1H, t-like, J=7.5Hz), 7.20(1H, dd, J=8.9, 2.3Hz),
		7.27(1H, dd, J=8.9, 2.7Hz), 7.37-7.41(4H, m), 7.57(1H, t,
		J=8Hz), 7.77(1H, d, J=9.2Hz), 7.86(1H, d, J=8.9Hz),
		7.96(1H, dd, J=7.9, 1.3Hz), 8.52(1H, d, J=8.3Hz),
		11.18(1H, brs).
7	21	11.08(brs, 1H), 8.73(dd, 1H, J=8.6, 0.7Hz), 8.00(dd, 1H,	6
methyl		J=8.1, 1.3Hz), 7.69(d, 1H, J=8.9Hz), 7.60(d, 1H, J=9.6Hz),
ester		7.53(t, 1H, J=8.5Hz), 7.37-7.03(m, 9H), 4.22(t, 2H,
		J=5.6Hz), 3.89(s, 3H), 3.75(t, 4H, J=4.6Hz), 3.75(s, 2H),
		2.87(t, 2H, J=5.6Hz), 2.62(t, 4H, J=4.6Hz).
9	40	1 H-NMR (DMSO-d6); δ 13.58(brs, 1H), 11.16(s, 1H),	8
		8.53(d, 1H, J=8.6Hz), 7.96(dd, 1H, J=7.9, 1.7Hz),
		7.84(d, 1H, J=8.6Hz), 7.78(d, 1H, J=8.9Hz), 7.58(m,
		1H), 7.41(d, 2H, J=8.6Hz), 7.26-7.02(m, 7H), 4.53(brs,
		1H), 4.11(t, 2H, J=6.3Hz), 3.78(s, 2H), 3.58(t, 2H, J=6.0Hz),
		1.90(quint, 2H, J=6.3Hz).
9	47	11.10(brs, 1H), 8.72(dd, 1H, J=8.58, 0.99Hz), 8.00(dd,	6
methyl		1H, J=8.24, 1.65Hz), 7.71(d, 1H, J=8.25Hz), 7.68(d, 1H,
ester		J=7.91Hz), 7.52(ddd, 1H, J=8.58, 7.25, 1.65Hz), 7.37(d,
		2H, J=8.57Hz), 7.20(d, 1H, J=2.31Hz), 7.12-6.99(m,
		6H), 4.18(t, 2H, J=5.93Hz), 3.88(s, 3H), 3.88(t, 2H,
		J=4.95Hz), 3.75(s, 2H), 2.08(m, 2H).
10	81	1 H-NMR (DMSO-d6); δ 13.56(brs, 1H), 11.19(s, 1H),	8
		8.54(d, 1H, J=8.6Hz), 7.96(dd, 1H, J=7.9, 1.7Hz),
		7.85(d, 1H, J=8.6Hz), 7.79(d, 1H, J=8.9Hz), 7.57(m,
		1H), 7.41(d, 2H, J=8.6Hz), 7.23-7.04(m, 7H), 4.15(t, 2H,
		J=4.6Hz), 3.78(s, 2H), 3.73(t, 2H, J=4.6Hz), 3.51(q, 2H,
		J=7.0Hz), 1.14(t, 3H, J=7.0Hz).
10	93	11.10(brs, 1H), 8.73(d, 1H, J=8.25Hz), 7.99(dd, 1H,	6
methyl		J=7.91, 1.65Hz), 7.70(d, 1H, J=8.25Hz), 7.67(d, 1H,
ester		J=8.24Hz), 7.52(ddd, 1H, J=8.58, 7.25, 1.32Hz), 7.37(d,
		2H, J=8.57Hz), 7.21(d, 1H, J=1.98Hz), 7.13-7.03(m,
		5H), 6.99(d, 1H, J=2.64Hz), 4.18(t, 2H, J=4.61Hz),
		3.87(s, 3H), 3.82(t, 2H, J=4.62Hz), 3.75(s, 2H), 3.60(q,
		2H, J=6.93Hz), 1.24(t, 3H, J=6.93Hz).

[0603]

TABLE 47
11	33	1 H-NMR (DMSO-d6); δ 14.05(brs, 1H), 8.46(d, 1H, J=8.2Hz),	11
		7.95(dd, 1H, J=7.8, 1.5Hz), 7.82(d, 1H, J=8.9Hz),
		7.74(d, 1H, J=9.2Hz), 7.40(d, 2H, J=8.6Hz),
		7.30-7.20(m, 3H), 7.14-6.94(m, 5H), 4.13(t, 2H, J=5.5Hz),
		3.64(s, 2H), 3.07(brm, 4H), 2.74(brm, 2H), 2.70(brs,
		4H).
11	48	11.10(brs, 1H), 8.73(dd, 1H, J=8.58, 0.99Hz), 8.01(dd,	10
methyl		1H, J=8.35, 1.65Hz), 7.71(d, 1H, J=8.58Hz), 7.68(d, 1H,
ester		J=7.91Hz), 7.53(ddd, 1H, J=8.57, 7.26, 1.32Hz), 7.38(d,
		2H, J=8.90Hz), 7.21(d, 1H, J=1.98Hz), 7.13-7.04(m,
		5H), 6.99(d, 1H, J=2.31Hz), 4.18(t, 2H, J=5.94Hz),
		3.89(s, 3H), 3.76(s, 2H), 2.92(t, 4H, J=4.62Hz), 2.84(t,
		2H, J=5.94Hz), 2.56(brm, 4H).
12	32	1 H-NMR (DMSO-d6); δ 8.48(d, 1H, J=8.6Hz), 7.95(d,	11
		1H, J=7.9Hz), 7.84(d, 1H, J=8.9Hz), 7.78(d, 1H, J=8.9Hz),
		7.66-7.57(m, 1H), 7.45-7.38(m, 2H), 7.28-7.02(m,
		7H), 4.17(t, 2H, J=5.7Hz), 3.72(s, 2H), 3.61-3.56(m, 8H),
		2.75(t, 2H, J=5.7Hz).
12	78	11.11(brs, 1H), 8.73(dd, 1H, J=8.58, 0.66Hz), 8.01(dd,	10
methyl		1H, J=8.25, 1.65Hz), 7.72(d, 1H, J=8.25Hz), 7.69(d, 1H,
ester		J=7.91Hz), 7.53(ddd, 1H, J=8.57, 7.26, 1.65Hz), 7.38(d,
		2H, J=8.57Hz), 7.21(d, 1H, J=2.31Hz), 7.13-7.04(m,
		5H), 6.99(d, 1H, J=2.31Hz), 4.19(t, 2H, J=5.93Hz),
		3.89(s, 3H), 3.76(s, 2H), 3.74(t, 4H, J=4.62Hz), 2.85(t,
		2H, J=5.94Hz), 2.60(t, 4H, J=4.62Hz).
13	69	1 H-NMR (DMSO-d6); δ 8.57(dd, 2H, J=4.5, 1.5Hz),	11
		8.48(d, 1H, J=8.3Hz), 7.97(dd, 1H, J=7.9, 1.6Hz), 7.85(t,
		2H, J=9.2Hz), 7.65-7.54(m, 2H), 7.47-7.36(m, 5H),
		7.24-7.05(m, 5H), 5.27(s, 2H), 3.71(s, 2H).
13	85	11.12(brs, 1H), 8.73(d, 1H, J=8.58Hz), 8.62(dd, 2H,	10
methyl		J=4.62, 1.65Hz), 8.01(dd, 1H, J=8.25, 1.65Hz),
ester		7.75-7.36(m, 8H), 7.19-7.01(m, 6H), 5.17(s, 2H), 3.89(s,
		3H), 3.76(s, 2H).
14	10	1 H-NMR (DMSO-d6); δ 13.19(brs, 1H), 8.49(d, 1H, J=7.6Hz),	11
		7.97(d, 1H, J=7.9Hz), 7.84(d, 1H, J=8.9Hz), 7.78(d,
		1H, J=8.9Hz), 7.37(d, 2H, J=8.6Hz), 7.40-7.33(m, 2H),
		7.25(s, 1H), 7.13(dd, 1H, J=8.9, 2.5Hz), 7.05-6.96(m,
		2H), 7.05(d, 2H, J=8.6Hz), 4.37(2H, m), 3.67(s, 2H),
		3.22(brs, 2H), 2.98(brs, 4H), 1.67(brs, 4H), 1.5-1.4(brs,
		2H).

[0604]

TABLE 48
14	60	11.10(brs, 1H), 8.73(d, 1H, J=8.25Hz), 8.01(dd, 1H,	10
methyl		J=8.25, 1.65Hz), 7.71(d, 1H, J=8.58Hz), 7.68(d, 1H,
ester		J=8.24Hz), 7.53(dd, 1H, J=8.57, 7.26Hz), 7.37(d, 2H,
		J=8.24Hz), 7.21(d, 1H, J=1.98Hz), 7.12-7.04(m, 5H),
		6.99(d, 1H, J=2.31Hz), 4.18(t, 2H, J=5.93Hz), 3.89(s,
		3H), 3.76(s, 2H), 2.81(t, 2H, J=5.94Hz), 2.52(t, 4H,
		J=4.95Hz), 1.65-1.56(brm, 4H), 1.47-1.43(brm, 2H).
16	100	1 H-NMR (DMSO-d6); δ 11.20(brs, 1H), 8.51(d, 1H, J=8.6Hz),	11
		7.96(dd, 1H, J=7.6, 1.7Hz), 7.84(d, 1H, J=8.9Hz),
		7.73(d, 1H, J=8.9Hz), 7.57(dd, 1H, J=8.6, 7.6Hz),
		7.21-7.39(m, 10H), 7.11-7.16(m, 2H), 7.02(d, 2H, J=8.6Hz),
		4.52(brs, 3H), 3.75(s, 2H), 3.49(brm, 1H),
		2.03-2.09(brm, 4H), 1.47-1.54(m, 4H).
16	29	11.08(brs, 1H), 8.72(dd, 1H, J=8.6, 1.0Hz), 8.00(dd, 1H,	10
methyl		J=7.9, 1.7Hz), 7.69(d, 1H, J=8.9Hz), 7.60(d, 1H, J=8.9Hz),
ester		7.53(ddd, 1H, J=8.6, 7.3, 1.7Hz), 7.24-7.37(m, 9H),
		7.03-7.22(m, 3H), 7.04(d, 2H, J=8.6Hz), 4.57(s, 2H),
		4.43(brm, 1H), 3.88(s, 3H), 3.75(s, 2H), 3.54(brm, 1H),
		2.14-2.17(brm, 4H), 1.55-1.64(m, 4H).
17	96	1 H-NMR (DMSO-d6); δ 13.90(br, 1H), 8.44(d, 1H, J=8.2Hz),	26
		7.99(d, 1H, J=7.6Hz), 7.82(d, 1H, J=8.9Hz), 7.74(d,
		1H, J=8.9Hz), 7.27-7.37(m, 6H), 7.22(dd, 1H, J=8.9, 2.3Hz),
		7.11(d, 1H, J=8.9, 2.3Hz), 7.00(d, 2H, J=8.6Hz),
		6.95(d, 1H, J=7.3Hz), 4.59(d, 1H, J=3.6Hz), 4.43(brm,
		1H), 3.62(s, 2H), 3.56(brm, 1H), 2.05(brm, 2H), 1.88(brm,
		2H), 1.30-1.52(m, 4H).
18	—	1 H-NMR (DMSO-d6); δ 11.27(brs, 1H), 8.50(d, 1H,	19
		J=8.58Hz), 7.99-7.94(m, 3H), 7.83(d, 1H, J=8.90Hz),
		7.76(d, 1H, J=8.91Hz), 7.56(d, 1H, J=8.25, 7.59Hz),
		7.39-7.10(m, 5H), 7.02(d, 2H, J=8.58Hz), 4.71(br, 1H),
		3.75(s, 2H), 3.17(brm, 1H), 2.06-1.91(m, 2H),
		1.78-1.60(m, 6H).
18	66	11.07(brs, 1H), 8.72(d, 1H, J=8.41Hz), 8.00(dd, 1H,	18
methyl		J=8.08, 1.65Hz), 7.68-7.49(m, 3H), 7.36-7.02(m, 9H),
ester		4.58(br, 1H), 3.88(s, 3H), 3.74(s, 2H), 2.80(m, 1H),
		2.09-2.04(m, 2H), 1.70-1.46(m, 6H).

[0605]

TABLE 49
19	34	1 H-NMR (DMSO-d6); δ 13.58(br, 1H), 11.27(brs, 1H),	19
		8.51(d, 1H, J=8.25Hz), 7.97-7.80(m, 5H), 7.57(dd, 1H,
		J=8.25, 7.59Hz), 7.41(d, 2H, J=7.26Hz), 7.26-7.05(m,
		5H), 4.68(br, 1H), 3.77(s, 2H), 3. 13(brm, 1H),
		2.07-2.02(m, 2H), 1.75-1.60(m, 6H).
19	71	11.10(brs, 1H), 8.72(d, 1H, J=8.58Hz), 7.99(dd, 1H,	18
methyl		J=7.91, 1.65Hz), 7.68-7.63(m, 2H), 7.52(dd, 1H, J=7.26,
ester		6.92Hz), 7.36(d, 2H, J=8.58Hz), 7.16-6.97(m, 7H),
		4.60(br, 1H), 3.87(s, 3H), 3.75(s, 2H), 3.27(m, 1H),
		2.21-2.16(m, 2H), 2.02(m, 4H), 1.61(m, 2H).
20	42%	1 H-NMR (DMSO-d6); δ 9.87(brs, 1H), 8.43(d, 1H, J=8.37Hz),	11
	(yield	8.00(d, 1H, J=7.83Hz), 7.82(d, 1H, J=9.45Hz),
	form	7.75(d, 1H, J=8.91Hz), 7.51(d, 2H, J=7.83Hz), 7.35(d,
	Ex. 6)	4H, J=8.37Hz), 7.24(m, 4H), 7.11(d, 1H, J=9.45Hz),
		6.94(m, 3H), 4.24(t, 2H, J=6.48Hz), 3.59(s, 2H), 3.03(t,
		2H, J=6.21Hz), 2.02(s, 3H).
20	—	11.10(brs, 1H), 8.71(d, 1H, J=8.64Hz), 8.23(brs, 1H),	10
methyl		7.99(d, 1H, J=8.10Hz), 7.69-7.02(m, 16H), 4.22(t, 2H,
ester		J=7.02Hz), 3.87(s, 3H), 3.74(s, 2H), 3.09(t, 2H, J=7.02Hz),
		2.12(s, 3H).
21	87	1 H-NMR (DMSO-d6); δ 3.36(3H, s), 3.74(2H, t, J=4.6Hz),	8
		4.23(2H, t, J=4.6Hz), 7.16-7.21(4H, m), 7.30(1H,
		dd, J=8.9, 2.3Hz), 7.38(1H, s), 7.49(1H, s), 7.64(1H, t,
		J=8.6Hz), 7.85(1H, d, J=8.9Hz), 7.90(1H, d, J=8.9Hz),
		7.99(2H, d, J=8.6Hz), 8.23(1H, d, J=7.6Hz), 8.73(1H, d,
		J=8.2Hz), 12.21(1H, brs).
21	44	12.00(brs, 1H), 8.93(d, 1H, J=8.9Hz), 8.23-8.00(m, 3H),	6
methyl		7.75(d, 1H, J=8.9Hz), 7.66(d, 1H, J=8.9Hz), 7.59(t, 1H,
ester		J=7.9Hz), 7.41(d, 1H, J=2.3Hz), 7.23-7.08(m, 6H),
		4.23(t, 2H, J=4.7Hz), 3.92(s, 3H), 3.82(t, 2H, J=4.7Hz),
		3.48(s, 3H).
22	82	1 H-NMR (DMSO-d6); δ 1.14(3H, t, J=6.9Hz), 3.52(2H,	8
		q, J=6.9Hz), 3.76(2H, t, J=4.3Hz), 4.20(2H, t, J=4.3Hz),
		7.16-7.22(4H, m), 7.31(1H, dd, J=2.3, 8.9Hz), 7.39(1H, d,
		J=2.3Hz), 7.57(1H, d, J=2.6Hz), 7.65(1H, dt, J=1.6, 8.6Hz),
		7.81(1H, d, J=9.2Hz), 7.90(1H, d, J=8.9Hz),
		7.97(2H, d, J=8.6Hz), 8.04(1H, dd, J=7.9, 1.7Hz),
		8.69(1H, d, J=7.6Hz), 12.15(1H, s), 13.7(1H, br s).

[0606]

TABLE 50
22	61	12.01(brs, 1H), 8.93(d, 1H, J=8.6Hz), 8.10-8.01(m, 3H),	6
methyl		7.76(d, 1H, J=8.9Hz), 7.68-7.58(m, 2H), 7.42(d, 1H,
ester		J=2.3Hz), 7.25-7.09(m, 6H), 4.26(t, 2H, J=4.6Hz),
		3.95(s, 3H), 3.88(t, 2H, J=4.6Hz), 3.65(q, 2H, J=6.9Hz),
		1.28(t, 3H, J=6.9Hz).
23	93	1 H-NMR (DMSO-d6); δ 1.51-1.61(2H, m), 1.70(2H,	8
		quint, J=7.4Hz), 1.83(2H, quint, J=7.6Hz), 2.36(2H, t,
		J=7.3Hz), 4.10(2H, t, J=6.6Hz), 7.01(1H, t, J=7.3Hz),
		7.15-7.37(8H, m), 7.56-7.68(m, 4H), 7.79(1H, d, J=8.6Hz),
		7.90(1H, d, J=8.6Hz), 7.98(1H, d, J=8.9Hz),
		8.05(1H, d, J=7.9Hz), 8.72(1H, d, J=8.6Hz), 9.86(1H, s
		br), 12.16(1H, s br).
23	89	12.01(brs, 1H), 8.92(d, 1H, J=8.1Hz), 8.10-8.01(m, 3H),	6
methyl		7.75(d, 1H, J=8.9Hz), 7.67-7.59(m, 2H), 7.50(d, 2H,
ester		J=7.9Hz), 7.40(t, 1H, J=2.3Hz), 7.32(t, 1H, J=8.3Hz),
		7.26-7.08(m, 9H), 4.10(t, 2H, J=6.2Hz), 3.95(s, 3H),
		2.42(t, 2H, J=7.3Hz), 1.94-1.80(m, 4H), 1.68-1.58(m, 2H).
24	88	1 H-NMR (DMSO-d6); δ 3.39(2H, t, J=5.6Hz), 4.06(2H,	8
		t, J=5.6Hz), 4.98(2H, s), 7.09-7.16(4H, m), 7.23-7.34(2H,
		m), 7.28(5H, s), 7.51-7.56(2H, m), 7.75(1H, d, J=8.1Hz),
		7.83(1H, d, J=8.1Hz), 7.92(2H, d, J=8.2Hz), 7.98(1H, d,
		J=8.3Hz), 8.63(1H, d, J=8.2Hz), 12.11(1H, s br).
24	97	11.77(s, 1H), 8.67(d, 1H, J=7.9Hz), 8.10-7.99(m, 3H),	6
methyl		7.76(d, 1H, J=8.9Hz), 7.64(d, 1H, J=2.3Hz),
ester		7.50-7.44(m, 2H), 7.44-7.36(m, 5H), 7.32-7.16(m, 6H),
		5.14(s, 2H), 4.23(t, 2H, J=6.0Hz), 3.99(s, 3H), 3.55(dt,
		2H, J=7.6, 6.0Hz).
25	31	1 H-NMR (DMSO-d6); δ 12.32(brs, 1H), 8.70(d, 1H,	8
		J=8.2Hz), 8.12(d, 1H, J=8.7Hz), 7.99(d, 2H, J=8.6Hz),
		7.94(d, 1H, J=8.6Hz), 7.82(d, 1H, J=8.9Hz), 7.64(t, 1H,
		J=7.3Hz), 7.56(s, 1H), 7.40(d, 1H, J=2.3Hz), 7.32(dd,
		1H, J=8.9, 2.3Hz), 7.22-7.16(m, 4H), 4.19(m, 2H),
		3.86(m, 4H), 3.25-3.19(m, 6H), 2.23(m, 2H).
25	94	12.01(brs, 1H), 8.93(d, 1H, J=8.6Hz), 8.23-8.01(m, 3H),	6
methyl		7.75(d, 1H, J=8.9Hz), 7.64(d, 1H, J=8.9Hz), 7.60(t, 1H,
ester		J=7.3Hz), 7.41(d, 1H, J=2.3Hz), 7.17-7.09(m, 6H),
		4.16(t, 2H, J=6.9Hz), 3.95(s, 3H), 3.74(t, 4H, J=4.6Hz),
		2.58(t, 2H, J=6.9Hz), 2.50(t, 4H, J=4.6Hz), 2.05(tt, 2H, J=6.9, 6.9Hz).

[0607]

TABLE 51
26	98	1 H-NMR (DMSO-d6); δ 8.79(d, 1H, J=8.3Hz), 8.14(d,	8
		1H, J=7.9Hz), 8.07(d, 2H, J=7.9Hz), 7.99(d, 1H, J=8.9Hz),
		7.90(d, 1H, J=9.2Hz), 7.74(t, 1H, J=7.6Hz), 7.66(d,
		1H, J=2.3Hz), 7.48-7.39(m, 7H), 7.27(d, 4H, J=8.6Hz),
		5.11(s, 2H), 4.20(t, 2H, J=5.9Hz), 3.31(q, 2H, J=6.3Hz),
		2.08-2.00(m, 2H).
26	66	12.01(brs, 1H), 8.93(dd, 1H, J=8.6, 1.0Hz), 8.10-8.01(m,	6
methyl		3H), 7.75(d, 1H, J=8.9Hz), 7.70-7.57(m, 2H),
ester		7.42-7.31(m, 5H), 7.23-7.09(m, 7H), 5.12(s, 2H), 4.13(t,
		2H, J=6.3Hz), 3.95(s, 3H), 3.47(q, 2H, J=6.6Hz), 2.09(t, 2H, J=6.6Hz).
27	68	1 H-NMR (DMSO-d6); δ 2.14(quint, J=6.6Hz, 2H),	8
		2.62(t, J=7.3Hz, 2H), 4.16(t, J=6.3Hz, 2H), 7.11-7.22(m,
		5H), 7.30(dd, J=2.6, 8.9Hz, 1H), 7.39(d, J=2.3Hz, 1H),
		7.55-7.68(m, 3H), 7.79(d, J=9.2Hz, 1H), 7.89(d, J=8.9Hz,
		1H), 7.98(d, J=8.9Hz, 3H), 8.04(dd, J=1.0, 8.3Hz,
		1H), 8.49(d, J=8.6Hz, 1H), 8.69(d, J=7.9Hz, 1H),
		11.18(s, 1H), 12.15(s, 1H), 13.4-13.8(br, 2H).
27	82	12.01(brs, 1H), 11.16(brs, 1H), 8.92(dd, 1H, J=8.6, 1.0Hz),	6
methyl		8.75(dd, 1H, J=8.6, 1.0Hz), 8.10-8.00(m, 4H),
ester		7.74(d, 1H, J=8.9Hz), 7.66-7.52(m, 3H), 7.41(d, 1H,
methyl		J=2.3Hz), 7.25-7.05(m, 7H), 4.21(t, 2H, J=5.9Hz),
ester		3.95(s, 3H), 3.88(s, 3H), 2.73(t, 2H, J=6.9Hz),
		2.32(quint, 2H, J=6.3Hz).
28	74	1 H-NMR (DMSO-d6); δ 1.93(quint, J=5.9Hz, 2H),	8
		3.59(t, J=5.9Hz, 2H), 4.15(t, J=6.3Hz, 2H), 4.58(m, 1H),
		7.15-7.21(m, 4H), 7.31(dd, J=2.6, 8.9Hz, 1H), 7.39(d,
		J=2.0Hz, 1H), 7.56(d, J=2.3Hz, 1H), 7.64(t, J=7.6Hz,
		1H), 7.80(d, J=9.2Hz, 1H), 7.91(d, J=9.2Hz, 1H), 7.97(d,
		J=8.9Hz, 2H), 8.04(dd, J=1.7, 7.9Hz, 1H), 8.69(d, J=7.6,
		1H), 12.21(br.s, 1H), 13.79(br.s, 1H).
28	31	12.02(brs, 1H), 8.93(d, 1H, J=7.9Hz), 8.09(dd, 1H, J=7.9,	6
methyl		1.3Hz), 8.04(d, 2H, J=8.6Hz), 7.77(d, 1H, J=8.9Hz),
ester		7.67(d, 1H, J=8.2Hz), 7.64-7.59(m, 1H), 7.42(d, 1H,
		J=2.6Hz), 7.24-7.10(m, 6H), 4.27(t, 2H, J=5.9Hz),
		3.96(s, 3H), 3.93(t, 2H, J=5.9Hz), 2.14(quint, 2H, J=5.9Hz).

[0608]

TABLE 52
29	21	1 H-NMR (DMSO-d6); δ 3.15-3.50(br, 4H), 3.50-3.70(br,	8
		2H), 3.80-4.00(br, 4H), 4.50(t-like, 2H), 7.16-7.28(m, 4H),
		7.35(dd, J=2.6, 8.9Hz, 1H), 7.48(d, J=2.0Hz, 1H),
		7.59(d, J=2.3Hz, 1H), 7.66(t, J=8.9Hz, 1H), 7.86(d,
		J=9.2Hz, 1H), 7.93(d, J=8.9Hz, 1H), 7.98(d, J=8.9Hz,
		2H), 8.05(dd, J=1.7, 7.9Hz, 1H), 8.69(d, J=7.9Hz, 1H),12.14(s, 1H).
29	15	12.02(brs, 1H), 8.93(dd, 1H, J=8.6, 1.0Hz), 8.09(dd, 1H,	6
methyl		J=7.9, 1.7Hz), 8.04(d, 2H, J=8.9Hz), 7.76(d, 1H, J=8.9Hz),
ester		7.67(d, 1H, J=8.2Hz), 7.64-7.58(m, 1H), 7.42(d, 1H,
		J=2.3Hz), 7.26-7.09(m, 6H), 4.25(t, 2H, J=5.6Hz),
		3.95(s, 3H), 3.79-3.75(m, 4H), 2.89(t, 2H, J=5.6Hz),
		2.64(t, 4H, J=4.6Hz).
30	82	1 H-NMR (DMSO-d6); δ 1.33-1.52(6H, m), 1.76-1.82(2H,	8
		m), 3.37-3.43(2H, m), 4.08(2H, t, J=6.6Hz),
		7.15-7.22(4H, m), 7.30(1H, dd, J=8.9, 2.3Hz), 7.37(1H,
		s), 7.55(1H, d, J=2.3Hz), 7.66(1H, t, J=7.4Hz), 7.80(1H,
		d, J=9.2Hz), 7.91(1H, d, J=8.9Hz), 7.98(2H, d, J=8.9Hz),
		8.05(1H, d, J=8.3Hz), 8.71(1H, d, J=8.6Hz),
		12.18(1H, s br).
31	71	1 H-NMR (DMSO-d6); δ 12.33(brs, 1H), 8.79(d, 1H,	8
		J=8.3Hz), 8.14(dd, 1H, J=7.9, 1.3Hz), 8.07(d, 2H, J=8.9Hz),
		7.99(d, 1H, J=9.2Hz), 7.90(d, 1H, J=9.2Hz), 7.74(t,
		1H, J=8.6Hz), 7.66(d, 1H, J=2.3Hz), 7.46(d, 1H, J=2.3Hz),
		7.41(dd, 1H, J=8.9, 2.3Hz), 7.27(d, 4H, J=8.9Hz),
		7.05(t, 1H, J=5.9Hz), 4.18(t, 2H, J=6.6Hz), 3.21(q, 2H,
		J=6.6Hz), 1.99(t, 2H, J=6.6Hz), 1.47(s, 9H).
31	100	12.02(brs, 1H), 8.93(d, 1H, J=8.9Hz), 8.10-8.07(m, 1H),	6
methyl		8.04(d, 2H, J=8.6Hz), 7.76(d, 1H, J=8.9Hz), 7.67(d, 1H,
ester		J=9.9Hz), 7.61(t, 1H, J=8.9Hz), 7.42(d, 1H, J=2.3Hz),
		7.24-7.10(m, 6H), 4.79(brs, 1H), 4.15(t, 2H, J=6.3Hz),
		3.96(s, 3H), 3.39(q, 2H, J=6.3Hz), 2.10-2.05(m, 2H),
		1.46(s, 9H).
32	91	1 H-NMR (DMSO-d6); δ 1.40-1.53(m, 2H), 1.53-1.65(m,	8
		2H), 1.78(quint, J=6.3Hz, 2H), 2.25(t, J=7.3Hz, 2H),
		4.07(t, J=6.3Hz, 2H), 7.15-7.22(m, 4H), 7.30(dd, J=2.3,
		8.9Hz, 1H), 7.38(d, J=2.3Hz, 1H), 7.56(d, J=2.3Hz,
		1H), 7.65(t, J=8.6Hz, 1H), 7.79(d, J=9.2Hz, 1H), 7.90(d,
		J=8.9Hz, 1H), 7.97(d, J=8.9Hz, 2H), 8.04(dd, J=1.7, 7.9Hz,
		1H), 8.69(d, J=8.6Hz, 1H), 12.05(br.s, 1H), 12.17(s,
		1H).

[0609]

TABLE 53
32	67	12.02(brs, 1H), 8.93(d, 1H, J=8.3Hz), 8.09(dd, 1H, J=8.3,	6
methyl		1.7Hz), 8.04(d, 2H, J=8.6Hz), 7.76(d, 1H, J=8.9Hz),
ester		7.68-7.58(m, 2H), 7.42(d, 1H, J=2.3Hz), 7.25-7.10(m,
ethyl		6H), 4.14(q, 2H, J=7.3Hz), 4.09(t, 2H, J=7.3Hz), 3.95(s,
ester		3H), 2.37(t, 2H, J=7.3Hz), 1.89(quint, 2H, J=7.3Hz),
		1.75(quint, 2H, J=7.3Hz), 1.62-1.51(m, 2H), 1.27(t, 3H, J=7.3Hz).
33	33	1 H-NMR (DMSO-d6); δ 2.07(quint, J=5.9Hz, 2H),	37
		2.95-3.10(m, 2H), 4.18(t, J=5.9, 2H), 7.15-7.23(m, 4H),
		7.33(dd, J=2.3, 8.9Hz, 1H), 7.38(d, J=2.0Hz, 1H),
		7.57(d, J=2.6Hz, 1H), 7.61-7.64(m, 1H), 7.82(d, J=8.9Hz,
		1H), 7.91(d, J=9.2Hz, 1H), 7.98(d, J=8.9Hz, 2H),
		8.04(d, J=8.3Hz, 1H), 8.69(d, J=8.6Hz, 1H).
34	58	1 H-NMR (DMSO-d6); δ 1.13(t, 3H, J=6.92Hz), 3.50(q,	11
		2H, J=6.93Hz), 3.69(t, 2H, J=4.62Hz), 3.72(s, 2H),
		4.06(t, 2H, J=4.62Hz), 6.91(d, 2H, J=8.59Hz), 6.97(s,
		4H), 7.13(ddd, 1H, J=1.32, 7.59, 7.92Hz), 7.32(d, 2H,
		J=8.58Hz), 7.57(ddd, 1H, J=1.65, 6.93, 8.58Hz),
		7.95(dd, 1H, J=1.32, 7.91Hz), 8.50(d, 1H, J=8.25Hz),
		11.13(s, 1H), 13.56(br, 1H).
34	103	11.04(brs, 1H), 8.71(d, 1H, J=8.58Hz), 7.98(dd, 1H,	10
methyl		J=7.91, 1.65Hz), 7.50(ddd, 1H, J=8.58, 7.26, 1.65Hz),
ester		7.30(d, 2H, J=8.58Hz), 7.05(ddd, 1H, J=7.92, 7.26, 0.99Hz),
		7.00-6.87(m, 6H), 4.09(t, 2H, J=4.62Hz), 3.86(s,
		3H), 3.77(t, 2H, J=4.62Hz), 3.71(s, 2H), 3.60(q, 2H,
		J=6.91Hz), 1.24(t, 3H, J=6.91Hz).
35	58	1 H-NMR (DMSO-d6); δ 3.39(s, 3H), 3.72(s, 2H), 5.16(s,	8
		2H, 6.92(d, J=8.6Hz, 2H), 6.99(d, J=9.2Hz, 2H), 7.04(d,
		J=9.2Hz, 2H), 7.13(dd, J=6.9, 7.9Hz, 1H), 7.33(d, J=8.6Hz,
		2H), 7.57(ddd, J=1.7, 6.9, 8.6Hz, 1H), 7.95(dd,
		J=1.7, 7.9Hz, 1H), 8.50(d, J=8.6Hz, 1H), 11.17(s, 1H).
35	86	11.04(brs, 1H), 8.72(dd, 1H, J=8.6Hz, 1.0Hz), 7.98(dd,	6
methyl		1H, J=8.2, 1.7Hz), 7.51(ddd, 1H, J=8.6, 6.9, 1.7Hz),
ester		7.31(d, 2H, J=8.6Hz), 7.04(ddd, 1H, J=8.2, 6.9, 1.0Hz),
		7.00(d, 2H, J=6.3Hz), 6.98(d, 2H, J=6.3Hz), 6.97(d, 2H,
		J=8.6Hz), 5.13(s, 2H), 3.86(s, 3H), 3.72(s, 2H), 3.48(s,
		3H).

[0610]

TABLE 54
36	39	1.91-2.13(m, 4H), 2.76(s, 3H), 2.94-3.33(m, 4H), 3.73(s,	11
		2H), 4.62(br, 1H), 6.93(d, J=8.6Hz, 2H), 6.99(d, J=9.2Hz,
		2H), 7.04(d, J=9.2Hz, 2H), 7.13(dd, J=6.9, 8.3Hz,
		1H), 7.34(d, J=8.6Hz, 2H), 7.56(ddd, J=1.3, 6.9, 8.3Hz,
		1H), 7.95(dd, J=1.3, 8.3Hz, 1H), 8.50(d, J=8.3Hz, 1H).
36	100	11.04(brs, 1H), 8.72(d, 1H, J=8.6Hz), 7.99(dd, 1H, J=7.9Hz,	10
methyl		1.7Hz), 7.52(ddd, 1H, J=8.6, 7.3, 1.7Hz), 7.31(d, 2H,
ester		J=8.6Hz), 7.06(dd, 1H, J=7.9, 7.3Hz), 6.97(d, 2H, J=9.2Hz),
		6.96(d, 2H, J=8.6Hz), 6.87(d, 2H, J=9.2Hz),
		4.16-4.26(m, 1H), 3.87(s, 3H), 3.72(s, 2H), 2.54-2.70(m,
		2H), 2.30(s, 3H), 1.96-2.03(m, 2H), 1.77-1.90(m, 2H), 1.23-1.30(m,
		2H).
37	58	1 H-NMR (DMSO-d6); δ 3.71(s, 2H), 5.16(s, 2H), 6.90(d,	11
	yield	2H, J=8.24Hz), 7.02(d, 2H, J=4.95Hz), 7.02(d, 2H,
	from	J=4.95Hz), 7.11(dd, 1H, J=6.93, 7.92Hz), 7.32(d, 2H,
	Ex. 6	J=8.56Hz), 7.43(d, 2H, J=5.61Hz), 7.56(dd, 1H, J=6.93,
		8.58Hz), 7.94(d, 1H, J=7.59Hz), 8.49(d, 1H, J=8.25Hz),
		8.57(d, 2H, J=5.93Hz), 11.17(br, 1H).
37	100	11.07(br, 1H), 8.73(d, 1H, J=8.58Hz), 8.58(d, 2H, J=5.94Hz),	10
methyl		7.97(dd, 1H, J=8.24, 1.65Hz), 7.71-7.30(m, 5H),
ester		7.05-6.89(m, 7H), 5.03(s, 2H), 3.83(s, 3H), 3.71(s, 2H).
38	50	1 H-NMR (DMSO-d6); δ 3.34(br, 4H), 3.53(t, 2H, J=4.95Hz),	11
		3.72(s, 2H), 3.87(br, 4H), 4.37(t, 2H, J=4.95Hz),
		6.91(d, 2H, J=8.58Hz), 7.03(s, 4H), 7.13(ddd, 1H,
		J=1.32, 7.26, 7.59Hz), 7.33(d, 2H, J=8.91Hz), 7.57(ddd,
		1H, J=1.32, 7.26, 8.58Hz), 7.95(dd, 1H, J=1.65, 7.91Hz),
		8.49(d, 1H, J=7.59Hz), 11.11(s, 1H).
38	72	11.04(brs, 1H), 8.72(d, 1H, J=8.58Hz), 7.99(dd, 1H,	10
methyl		J=7.91, 1.32Hz), 7.51(ddd, 1H, J=8.58, 7.25, 1.32Hz),
ester		7.31(d, 2H, J=8.58Hz), 7.05(dd, 1H, J=7.91, 7.59Hz),
		7.00-6.85(m, 6H), 4.08(t, 2H, J=5.94Hz), 3.87(s, 3H),
		3.73(t, 4H, J=4.52Hz), 3.72(s, 2H), 2.79(t, 2H, J=5.94Hz),
		2.58(t, 4H, J=4.62Hz).
39	40	1 H-NMR (DMSO-d6); δ 2.16(br, 4H), 3.41(br, 4H),	11
		3.65(t, 2H, J=4.62Hz), 3.82(s, 2H), 4.40(t, 2H, J=4.97Hz),
		7.01(d, 2H, J=8.58Hz), 7.12(s, 4H), 7.22(dd, 1H,
		J=7.26, 8.54Hz), 7.43(d, 2H, J=8.58Hz), 7.66(dd, 1H,
		J=7.26, 8.24Hz), 8.04(d, 1H, J=7.92Hz), 8.58(d, 1H,
		J=8.25Hz), 11.26(s, 1H).

[0611]

TABLE 55
39	63	11.03(brs, 1H), 8..71(dd, 1H, J=8.58, 0.99Hz), 7.99(dd,	10
methyl		1H, J=8.25, 1.65Hz), 7.52(m, 1H), 7.31(d, 2H, J=8.59Hz),
ester		7.06(m, 1H), 7.01-6.85(m, 6H), 4.09(t, 2H, J=5.94Hz),
		3.87(s, 3H), 3.72(s, 2H), 2.91(t, 2H, J=5.94Hz),
		2.65(br, 4H), 1.82(t, 4H, J=3.63Hz).
40	50	1 H-NMR (DMSO-d6); δ 1.39-1.41(m, 2H), 1.51-1.55(m,	11
		4H), 2.50-2.53(m, 4H), 2.74(t, J=5.9Hz, 2H), 3.56(s, 2H),
		4.07(t, J=5.9Hz, 2H), 6.86(d, J=8.6Hz, 2H),
		6.91-6.97(m, 5H), 7.24-7.28(m, 1H), 7.30(d, J=8.6Hz,
		2H), 8.00(dd, J=1.7, 7.6Hz, 1H), 8.42(d, J=8.3Hz, 1H), 11.20(s, 1H).
40	69	11.04(brs, 1H), 8.72(d, 1H, J=8.3Hz), 7.98(dd, 1H, J=8.3Hz),	10
methyl		1.3Hz), 7.51(ddd, 1H, J=8.3, 7.3, 1.3Hz), 7.30(d, 2H,
ester		J=8.6Hz), 7.05(dd, 1H, J=8.3, 7.3Hz), 6.97(d, 2H, J=9.2Hz),
		6.95(d, 2H, J=8.6Hz), 6.87(d, 2H, J=9.2Hz), 4.08(t,
		2H, J=6.3Hz), 3.87(s, 3H), 3.72(s, 2H), 2.76(t, 2H, J=6.3Hz),
		2.51-2.52(m, 4H), 1.54-1.64(m, 6H).
41	15	1 H-NMR (DMSO-d6); δ 2.82(s, 3H), 3.50(br, 10H),	8
		3.73(s, 2H), 4.33(br, 2H), 6.91(d, J=8.6Hz, 2H), 7.03(s,
		4H), 7.14(dd, J=7.3, 7.9Hz, 1H), 7.34(d, J=8.6Hz, 2H),
		7.57(dd, J=7.3, 8.6Hz, 1H), 7.95(d, J=7.9Hz, 1H),
		8.50(d, J=8.6Hz, 1H), 11.12(s, 1H).
41	38	11.04(brs, 1H), 8.71(dd, 1H, J=8.6, 0.7Hz), 7.99(dd, 1H,
methyl		J=7.9, 1.7Hz), 7.52(ddd, 1H, J=8.6, 8.3, 1.7Hz), 7.31(d,
ester		2H, J=8.9Hz), 7.07(dd, 1H, J=8.3, 7.9, 0.7Hz), 6.98(d,
		2H, J=7.3Hz), 6.95(d, 2H, J=7.3Hz), 6.86(d, 2H, J=8.9Hz),
		4.08(t, 2H, J=5.9Hz), 3.88(S, 3H), 3.72(S, 2H),
		2.82(t, 2H, J=5.9Hz), 2.64(br, 4H), 2.51(br, 4H), 2.31(s,
		3H).
42		1 H-NMR (DMSO-d6); δ 1.43-1.56(m, 6H), 3.40(brm,	30
		4H), 3.57(s, 2H), 4.76(s, 2H), 6.86-6.99(m, 7H),
		7.24-7.32(m, 3H), 8.00(dd, J=1.7, 7.6Hz, 1H), 8.42(d,
		J=7.9Hz, 1H), 14.13(brs, 1H).
42	67	11.04(brs, 1H), 8.71(dd, 1H, J=8.6, 1.0Hz), 7.99(dd, 1H,	29
methyl		J=7.9, 1.7Hz), 7.52(ddd, 1H, J=8.6, 7.3, 1.7Hz), 7.31(dd,
ester		2H, J=8.6, 2.0Hz), 7.06(ddd, 1H, J=7.9, 7.3, 1.0Hz),
		6.98(d, 2H, J=9.2, 2.6Hz), 6.96(dd, 2H, J=9.2, 2.6Hz),
		6.92(d, 2H, J=8.6, 2.0Hz), 4.66(s, 2H), 3.87(S, 3H),
		3.72(S, 2H), 3.55-3.58(br, 2H), 3.46-3.50(br, 2H),
		1.57-1.68(br, 6H).

[0612]

TABLE 56
43	37	1 H-NMR (DMSO-d6); δ 3.72(2H, s), 4.30(4H, s),	11
		6.91(2H, d, J=8.6Hz), 6.92-7.01(8H, m), 7.12(1H, dd,
		J=7.9, 7.3Hz), 7.30(1H, t, J=7.3Hz), 7.32(2H, d, J=8.6Hz),
		7.56(1H, ddd, J=8.6, 7.3, 1.7Hz), 7.95(1H, dd,
		J=7.9, 1.7Hz), 8.50(1H, d, J=8.6Hz), 11.24(1H, brs),
		13.50-13.60(1H, br).
43	68	11.04(brs, 1H), 8.71(dd, 1H, J=8.6, 1.0Hz), 7.99(dd, 1H,	10
methyl		J=8.2, 1.7Hz), 7.52(ddd, 1H, J=8.6, 7.3, 1.7Hz),
ester		7.25-7.33(m, 4H), 7.06(ddd, 1H, J=8.2, 7.3, 1.0Hz),
		6.90-7.02(m, 9H), 4.31(s, 4H), 3.87(S, 3H), 3.72(S, 2H).
44	44	1 H-NMR (DMSO-d6); δ 1.59(m, 2H), 1.92(m, 2H),	11
	Yield	3.46(m, 2H), 3.58(s, 2H), 3.86(m, 2H), 4.48(m, 1H),
	from	6.88(d, 2H, J=8.58Hz), 6.92(m, 1H), 6.95(s, 4H), 7.26(m,
	Ex. 6	1H), 7.30(d, 2H, J=8.25Hz), 8.01(dd, 1H, J=1.65, 7.92Hz),
		8.43(d, 1H, J=8.24Hz), 13.84(br, 1H).
44	—	11.04(brs, 1H), 8.70(d, 1H, J=8.58Hz), 7.99(dd, 1H,	10
methyl		J=7.91, 1.65Hz), 7.52(ddd, 1H, J=8.57, 7.26, 1.65Hz),
ester		7.31(d, 2H, J=8.25Hz), 7.06(ddd, 1H, J=8.25, 7.25, 0.99Hz),
		6.99-6.91(m, 4H), 6.88(d, 2H, J=9.24Hz),
		4.40(quint, 1H, J=3.96Hz), 3.97(m, 2H), 3.87(s, 3H),
		3.72(s, 2H), 3.56(m, 2H), 2.06-1.96(m, 2H), 1.84-1.72(m, 2H).
45	70	1 H-NMR (DMSO-d6); δ 11.15(brs, 1H), 9.85(s, 1H),	11
		8.50(d, 1H, J=8.57Hz), 7.79(dd, 1H, J=7.91, 1.48Hz),
		7.56(dd, 1H, J=7.09, 6.76Hz), 7.49(d, 2H, J=8.24Hz),
		7.31(d, 2H, J=8.57Hz), 7.22(d, 2H, J=8.24Hz), 7.12(dd,
		1H, J=8.08, 7.09Hz), 6.95(s, 4H), 6.89(d, 2H, J=8.57Hz),
		4.12(t, 2H, J=6.76Hz), 3.71(s, 2H), 2.96(t, 2H, J=6.76Hz), 2.01(s, 3H).
45	79	11.03(brs, 1H), 8.69(dd, 1H, J=8.64, 1.08Hz), 7.97(dd,	10
methyl		1H, J=8.10, 1.62Hz), 7.67-7.42(m, 4H), 7.29(d, 2H,
ester		J=8.64Hz), 7.21(d, 2H, J=8.37Hz), 7.05(ddd, 1H,
		J=8.10, 7.29, 1.08Hz), 6.97-6.80(m, 5H), 4.10(t, 2H,
		J=7.02Hz), 3.86(s, 3H), 3.71(s, 2H), 3.03(t, 2H, J=7.02Hz), 2.14(s, 3H).
47	55	1 H-NMR (DMSO-d6) δ 2.61(s, 6H), 3.15(t, 2H, J=4.95Hz),	11
	Yield	3.60(s, 2H), 4.20(t, 2H, J=5.28Hz), 6.87(d, 2H,
	from	J=7.92Hz), 6.98-7.02(m, 5H), 7.28-7.39(m, 3H), 7.95(d,
	Ex 6	1H, J=6.92Hz), 8.44(d, 1H, J=8.25Hz), 13.11(br, 1H).

[0613]

TABLE 57
47	—	11.03(br, 1H), 8.71(dd, 1H, J=8.58, 0.99Hz), 7.98(dd, 1H,	10
methyl		J=8.24, 1.65Hz), 7.51(ddd, 1H, J=8.58, 7.25, 1.65Hz),
ester		7.31(d, 2H, J=8.58Hz), 7.05(ddd, 1H, J=8.24, 7.26, 0.99Hz),
		7.01-6.86(m, 6H), 4.04(t, 2H, J=5.61Hz), 3.87(s,
		3H), 3.72(s, 2H), 2.73(t, 2H, J=5.61Hz), 2.34(s, 6H).
89	32	1 H-NMR (DMSO-d6); δ 3.35(s, 6H), 4.12(t, 2H, J=4.29Hz),	11
		4.54(t, 2H, J=4.62Hz), 7.09-7.25(m, 7H), 7.68(dd,
		1H, J=7.25, 7.53Hz), 7.98(d, 2H, J=8.56Hz), 8.08(d, 1H,
		J=7.91Hz), 8.71(d, 1H, J=8.26Hz), 12.20(s, 1H).
89	105	11.98(brs, 1H), 8.91(d, 1H, J=8.57Hz), 8.06(dd, 1H,	10
methyl		J=7.92, 1.65Hz), 8.00(d, 2H, J=8.57Hz), 7.59(ddd, 1H,
ester		J=8.58, 7.26, 1.65Hz), 7.09(dd, 1H, J=7.59, 7.58Hz),
		7.03-6.92(m, 6H), 4.07(t, 2H, J=5.61Hz), 3.94(s, 3H),
		2.75(t, 2H, J=5.61Hz), 2.36(s, 6H).
90	54	1 H-NMR (DMSO-d6); δ 12.37(s, 1H), 8.78(d, 1H, J=8.58Hz),	11
		8.14(d, 1H, J=7.91Hz), 8.04(d, 2H, J=8.58Hz),
		7.73(dd, 1H, J=8.58, 6.93Hz), 7.28(dd, 1H, J=7.92, 7.59Hz),
		7.23-7.14(m, 6H), 4.36(t, 2H, J=4.95Hz), 3.84(t, 4H,
		J=4.95Hz), 3.26(br, 2H), 3.04(br, 4H).
90	83	11.98(s, 1H), 8.92(d, 1H, J=8.24Hz), 8.06(dd, 1H,	10
methyl		J=7.91, 1.32Hz), 8.00(d, 2H, J=8.56Hz), 7.59(ddd, 1H,
ester		J=8.58, 7.26, 1.32Hz), 7.10(dd, 1H, J=7.92, 7.25Hz),
		7.04-6.91(m, 6H), 4.11(t, 2H, J=5.62Hz), 3.94(s, 3H),
		3.75(t, 4H, J=4.62Hz), 2.82(t, 2H, J=5.62Hz), 2.59(t,
		4H, J=4.62Hz).
91	13	1 H-NMR (DMSO-d6); δ 3.20-3.90(br, 10H), 4.48(s, 2H),	11
	yield	7.15-7.32(m, 7H), 7.74(t, 1H, J=7.26Hz), 8.04(d, 2H,
	from	J=8.91Hz), 8.14(dd, 1H, J=1.32, 7.92Hz), 8.78(d, 1H,
	Ex. 6	J=7.92Hz), 9.61(br, 1H), 12.19(s, 1H).
92	50	1 H-NMR (DMSO-d6); δ 1.96(br, 4H), 2.80-3.80(br, 4H),	11
		3.58(t, 2H, J=4.94Hz), 4.35(t, 2H, J=4.94Hz),
		7.06-7.21(m, 7H), 7.64(ddd, 1H, J=1.65, 7.26, 8.24Hz),
		7.95(d, 2H, J=8.90Hz), 8.05(dd, 1H, J=1.65, 8.25Hz),
		8.69(d, 1H, J=7.92Hz), 10.55(br, 1H), 12.24(s, 1H).

[0614]

TABLE 58
92	54	11.98(brs, 1H), 8.92(d, 1H, J=8.26Hz), 8.06(dd, 1H,	10
methyl		J=7.91, 1.32Hz), 8.00(d, 1H, J=8.91Hz), 7.58(dd, 1H,
ester		J=7.26, 6.93Hz), 7.09(dd, 1H, J=7.91, 7.59Hz),
		7.04-6.92(m, 6H), 4.11(t, 2H, J=5.94Hz), 3.94(s, 3H),
		2.91(t, 2H, J=5.94Hz), 2.64(brm, 4H), 1.82(brm, 4H).
93	31	1 H-NMR (DMSO-d6); δ 1.42-1.83(br, 6H), 3.03(br, 2H),	11
		3.33(br, 2H), 3.48(br, 2H), 4.42(t, J=5.0Hz, 2H), 7.08(d,
		J=8.6Hz, 2H), 7.09(d, J=8.9Hz, 2H), 7.14(d, J=8.9Hz,
		2H), 7.19(dd, J=7.6, 8.6Hz, 1H), 7.65(ddd, J=1.3, 7.6, 7.9Hz),
		1H), 7.95(d, J=8.6Hz, 2H), 8.06(dd, J=1.3, 7.9Hz,
		1H), 8.70(d, J=8.6Hz, 1H), 10.37(br, 1H), 12.15(s, 1H),
		13.76(br, 1H).
93	100	11.98(s, 1H), 8.92(d, 1H, J=8.6Hz), 8.06(dd, 1H, J=8.2,	10
methyl		1.7Hz), 8.00(d, 2H, J=8.9Hz), 7.58(ddd, 1H, J=8.6, 7.3,
ester		1.7Hz), 7.09(dd, 1H, J=8.2, 7.3Hz), 6.99-7.03(m, 4H),
		6.93(d, 2H, J=9.2Hz), 4.10(t, 2H, J=5.9Hz), 3.94(S, 3H),
		2.78(t, 2H, J=5.9Hz), 2.50-2.54(m, 4H), 1.54-1.64(m,
		4H), 1.42-1.52(m, 2H).
94	100	1 H-NMR (DMSO-d6); δ 2.83(s, 3H), 3.46(br, 12H),	8
		4.37(br, 2H), 7.06-7.14(m, 6H), 7.19(dd, J=7.9, 8.6Hz,
		1H), 7.66(dd, J=7.3, 8.6Hz, 1H), 7.95(d, J=8.9Hz, 2H),
		8.06(dd, J=1.7, 7.9Hz, 1H), 8.70(d, J=7.3Hz, 1H), 12.12(s, 1H).
94	54	11.98(brs, 1H), 8.91(d, 1H, J=8.2Hz), 8.06(dd, 1H, J=8.2,	6
methyl		1.7Hz), 8.00(d, 2H, J=8.9Hz), 7.59(ddd, 1H, J=8.2, 7.3,
ester		1.7Hz), 7.10(dd, 1H, J=8.2, 7.3Hz), 7.00-7.03(m, 4H),
		6.93(d, 2H, J=9.2Hz), 4.11(t, 2H, J=5.9Hz), 3.94(S, 3H),
		2.84(t, 2H, J=5.9Hz), 2.65(br, 4H), 2.52,(br, 4H), 2.32(s, 3H).
121	98	1 H-NMR (DMSO-d6); δ 11.20(s, 1H), 8.57(d, 1H, J=8.4Hz),	21
		7.99(d, 1H, J=7.6Hz), 7.87-7.90(m, 2H), 7.75(d, 1H,
		J=6.8Hz), 7.54-7.65(m, 4H), 7.35(d, 2H, J=8.4Hz),
		7.13(t, 1H, J=7.6Hz), 6.92-6.99(m, 6H), 4.33(brs, 1H),
		3.74(s, 2H), 3.14(br, 1H), 1.71-1.82(brm, 2H),
		1.45-1.61(brm, 6H).
121	60	11.04(brs, 1H), 8.71(d, 1H, J=7.3Hz), 8.00(dd, 1H, J=7.8,	21
methyl		1.4Hz), 7.90(dd, 2H, J=8.1, 1.4Hz), 7.49-7.58(m, 4H),
ester		7.23-7.32(m, 3H), 7.07(ddd, 1H, J=8.1, 7.3, 1.4Hz),
		6.93-6.96(m, 4H), 6.80-6.87(d, 2H, J=9.2Hz), 4.47(d, 1H,
		J=7.6Hz), 4.31(br, 1H), 3.88(s, 3H), 3.72(s, 2H),
		3.31(brm, 1H), 1.90-1.93(m, 2H), 1.58-1.66(m, 6H).

[0615]

TABLE 59
124	93	1 H-NMR (DMSO-d6); δ 11.20(s, 1H), 8.56(d, 1H, J=8.4Hz),	21
		8.04(d, 1H, J=0.8Hz), 7.96-7.99(m, 2H),
		7.80-7.85(m, 2H), 7.56(dd, 1H, J=7.8, 7.6Hz), 7.34(d, 2H,
		J=8.4Hz), 7.13(dd, 1H, J=8.4, 7.6Hz), 6.92-6.99(m, 6H),
		4.36(brs, 1H), 3.74(s, 2H), 3.20(br, 1H), 1.80-1.84(brm, 2H),
		1.50-1.60(brm, 6H).
124	44	11.05(brs, 1H), 8.71(d, 1H, J=8.4Hz), 7.96-8.01(m, 2H),
methyl		7.71(dd, 1H, J=8.4, 1.9Hz), 7.59(d, 1H, J=8.4Hz),
ester		7.52(ddd, 1H, J=8.4, 7.3, 1.9Hz), 7.30(d, 2H, J=8.4Hz),
		7.07(ddd, 1H, J=7.8, 7.3, 1.1Hz), 6.94-6.97(m, 4H),
		6.82(d, 2H, J=9.2Hz), 4.61(d, 1H, J=7.8Hz), 4.34(br,
		1H), 3.88(s, 3H), 3.72(s, 2H), 3.29(brm, 1H), 1.94-1.98(m, 2H),
		1.58-1.69(m, 6H).
207	82	1 H-NMR (DMSO-d6); δ 13.56(br, 1H), 11.13(s, 1H),	21
		8.51(d, 1H, J=8.4Hz), 7.95(dd, 1H, J=7.8, 1.6Hz),
		7.86(d, 1H, J=7.3Hz), 7.47-7.71(m, 5H), 7.33(dd, 2H,
		J=8.4Hz), 7.13(dd, 1H, J=7.8, 7.3Hz), 6.90-6.97(m, 6H),
		4.35(brs, 1H), 3.72(s, 2H), 3.16(br, 1H), 1.78(brm, 2H),
		1.45-1.58(brm, 6H).
207	77	11.05(brs, 1H), 8.71(d, 1H, J=8.4Hz), 7.99(dd, 1H, J=8.1,	21
methyl		1.6Hz), 7.70(d, 1H, J=7.8Hz), 7.46-7.63(m, 3H),
ester		7.24-7.32(m, 4H), 7.07(dd, 1H, J=8.1, 7.3Hz),
		6.93-6.97(m, 4H), 6.82(d, 2H, J=9.2Hz), 4.32(br, 1H),
		3.87(s, 3H), 3.72(s, 2H), 3.28-3.36(m, 1H), 1.93-1.96(m, 2H),
		1.55-1.68(m, 6H).
214	77	1 H-NMR (DMSO-d6); δ 13.54(br, 1H), 11.13(s, 1H),	21
		8.51(d, 1H, J=8.4Hz), 7.94-8.07(m, 6H), 7.57(ddd, 1H,
		J=8.4, 7.3, 1.4Hz), 7.32(d, 2H, J=8.4Hz), 7.13(dd, 1H,
		J=7.8, 7.3Hz), 6.90-6.98(m, 6H), 4.35(brs, 1H), 3.73(s,
		2H), 3.18(br, 1H), 1.79-1.80(brm, 2H), 1.46-1.59(m, 6H).
214	90	11.05(s, 1H), 8.71(dd, 1H, J=8.4, 0.8Hz), 8.03(d, 2H,	21
methyl		J=8.4Hz), 7.99(d, 1H, J=8.1, 1.4Hz), 7.77(d, 2H, J=8.4Hz),
ester		7.52(ddd, 1H, J=8.4, 7.3, 1.4Hz), 7.31(d, 2H, J=8.9Hz),
		7.07(ddd, 1H, J=8.1, 7.3, 0.8Hz), 6.91-7.04(m, 4H),
		6.81(d, 2H, J=6.8Hz), 4.93(d, 1H, J=7.6Hz), 4.32(br,
		1H), 3.87(s, 3H), 3.73(s, 2H), 3.27-3.33(m, 1H), 1.93-1.97(m, 2H),
		1.57-1.69(m, 6H).

[0616]

TABLE 60
215	80	1 H-NMR (DMSO-d6); δ 8.49(d, 1H, J=8.1Hz), 7.97(s,	21
		1H), 7.96(d, 2H, J=8.6Hz), 7.87(d, 1H, J=7.0Hz), 7.58(d,
		2H, J=8.6Hz), 7.51-7.57(m, 1H), 7.32(d, 2H, J=8.6Hz),
		7.11(dd, 1H, J=8.1, 7.3Hz), 6.89-6.97(m, 6H), 4.34(br,
		1H), 3.70(s, 2H), 3.15(br, 1H), 1.79(brm, 2H), 1.45-1.58(m, 6H).
215	93	11.05(s, 1H), 8.71(d, 1H, J=8.4Hz), 8.11(d, 1H, J=7.0Hz),	21
methyl		7.95-8.01(m, 3H), 7.51(ddd, 1H, J=8.4, 7.3, 1.6Hz),
ester		7.43(d, 1H, J=8.6Hz), 7.32(d, 2H, J=8.9Hz), 7.31(d, 2H,
		J=8.4Hz), 7.06(dd, 1H, J=7.3, 7.0Hz), 6.88-6.93(m, 4H),
		6.81(d, 2H, J=8.9Hz), 5.21(d, 1H, J=7.6Hz), 4.31(br,
		1H), 3.86(s, 3H), 3.73(s, 2H), 3.27-3.33(m, 1H),
		1.92-1.97(m, 2H), 1.57-1.71(m, 6H).
217	88	11.05(brs, 1H), 8.70(dd, 1H, J=8.3, 0.9Hz), 8.21(t, 1H,	21
methyl		J=1.4Hz), 8.13(ddd, 1H, J=7.8, 1.6, 1.4Hz), 7.99(dd, 1H,
ester		J=8.1, 1.6Hz), 7.83(ddd, 1H, J=8.1, 1.6, 1.4Hz), 7.64(dd,
		1H, J=8.1, 7.8Hz), 7.51(ddd, 1H, J=8.3, 7.3, 1.6Hz),
		7.31(d, 2H, J=8.3Hz), 7.06(ddd, 1H, J=8.1, 7.3, 0.9Hz),
		6.92-6.97(m, 4H), 6.81(d, 2H, J=7.0Hz), 5.32(d, 1H,
		J=7.6Hz), 4.32(brs, 1H), 3.87(s, 3H), 3.73(s, 2H),
		3.26-3.39(m, 1H), 1.93-1.98(m, 1H), 1.57-1.67(m, 6H).
410	37	1 H-NMR (DMSO-d6); δ 11.13(s, 1H), 8.45(d, 1H, J=8.57Hz),	11
		8.08(s, 1H), 7.96(d, 1H, J=7.92Hz), 7.81(d, 1H,
		J=8.25Hz), 7.57(dd, 1H, J=7.59, 7.92Hz), 7.18-7.03(m,
		5H), 6.97(d, 1H, J=8.25Hz), 4.39-4.37(m, 2H),
		4.00-3.70(brm, 4H), 3.80-3.77(m, 2H), 3.60-3.49(m, 2H),
		3.32(br, 4H).
410	44	11.17(brs, 1H), 8.68(d, 1H, J=8.58Hz), 8.16(d, 1H,	10
methyl		J=2.31Hz), 8.01(dd, 1H, J=1.32, 7.92Hz), 7.71(dd, 1H,
ester		J=2.31, 8.58Hz), 7.53(ddd, 1H, J=1.32, 7.26, 8.58Hz),
		7.11-7.05(m, 3H), 6.93-6.87(m, 3H), 4.12(t, 2H, J=5.61Hz),
		3.89(s, 3H), 3.76-3.73(m, 4H), 3.70(s, 2H), 2.82(t,
		2H, J=5.61Hz), 2.61-2.58(m, 4H).
411	45	1 H-NMR (DMSO-d6); δ 14.13(br, 1H), 8.41(d, 1H,	11
		J=8.25Hz), 8.06(d, 1H, J=2.31Hz), 8.00(dd, 1H, J=1.65,
		7.92Hz), 7.79(dd, 1H, J=2.31, 8.58Hz), 7.70(d, 1H,
		J=1.65Hz), 7.28(ddd, 1H, J=1.65, 7.26, 8.25Hz), 7.04(s,
		4H), 6.98-6.92(m, 2H), 6.59(d, 1H, J=3.30Hz), 6.48(dd,
		1H, J=1.98, 2.97Hz), 5.05(s, 2H), 3.62(s, 2H).

[0617]

TABLE 61
411	50	11.17(brs, 1H), 8.68(d, 1H, J=8.25Hz), 8.16(d, 1H,	10
methyl		J=1.98Hz), 8.00(dd, 1H, J=1.32, 7.92Hz), 7.72(dd, 1H,
ester		J=2.31, 8.58Hz), 7.53(ddd, 1H, J=1.65, 7.25, 8.58Hz),
		7.45(dd, 1H, J=0.99, 1.98Hz), 7.13-6.97(m, 5H), 6.88(d,
		1H, J=8.58Hz), 6.43(d, 1H, J=2.97Hz), 6.38(dd, 1H,
		J=1.98, 2.97Hz), 4.99(s, 2H), 3.89(s, 3H), 3.70(s, 2H).
412	15	1 H-NMR (DMSO-d6); δ 11.32(brs, 1H), 8.69(brs, 1H),	11
		8.56(brs, 1H), 8.45(d, 1H, J=8.25Hz), 8.09(s, 1H), 7.96(d,
		1H, J=7.92Hz), 7.89(d, 1H, J=7.92Hz), 7.81(d, 1H,
		J=8.58Hz), 7.63-7.52(m, 2H), 7.44(dd, 1H, J=7.25, 7.59Hz),
		7.16-7.07(m, 5H), 6.96(d, 1H, J=8.58Hz), 5.16(s, 2H), 3.76(s, 2H).
413	35	1 H-NMR (DMSO-d6); δ 14.00-13.00(br, 1H),	11
		11.90-11.30(br, 1H), 11.12(brs, 1H), 8.45(d, 1H, J=8.25Hz),
		8.08(s, 1H), 7.95(d, 1H, J=7.92Hz), 7.81(d, 1H,
		J=8.25Hz), 7.58(dd, 1H, J=7.59, 7.92Hz), 7.18-6.96(m,
		6H), 4.39(s, 2H), 3.77-3.44(br, 12H), 2.83(s, 3H).
413	72	11.17(brs, 1H), 8.68(d, 1H, J=8.58Hz), 8.16(d, 1H,	10
methyl		J=2.64Hz), 8.01(dd, 1H, J=1.65, 7.92Hz), 7.71(dd, 1H,
ester		J=2.64, 8.58Hz), 7.53(ddd, 1H, J=1.65, 7.26, 8.57Hz),
		7.11-7.04(m, 3H), 6.94-6.86(m, 3H), 4.10(t, 2H, J=5.61Hz),
		3.89(s, 3H), 3.70(s, 2H), 2.82(t, 2H, J=5.61Hz),
		2.63(br, 4H), 2.49(br, 4H), 2.30(s, 3H).
414	56	1 H-NMR (DMSO-d6); δ 13.90-13.30(br, 1H), 11.16(s,	11
		1H), 10.12-9.71(br, 1H), 8.45(d, 1H, J=8.25Hz), 8.08(d,
		1H, J=2.31Hz), 7.96(d, 1H, J=7.92Hz), 7.82(dd, 1H,
		J=2.31, 8.25Hz), 7.57(dd, 1H, J=7.26, 8.58Hz),
		7.17-6.96(m, 6H), 4.38(brt, 2H, J=4.95Hz), 3.77(s, 2H),
		3.58-3.38(brm, 4H), 3.15-2.86(m, 2H), 1.87-1.28(m, 6H).
414	72	11.16(brs, 1H), 8.68(d, 1H, J=8.58Hz), 8.16(d, 1H,	10
methyl		J=2.64Hz), 8.00(dd, 1H, J=1.65, 7.92Hz), 7.71(dd, 1H,
ester		J=2.64, 8.58Hz), 7.52(ddd, 1H, J=1.65, 7.26, 8.91Hz),
		7.10-7.03(m, 3H), 6.94-6.86(m, 3H), 4.10(t, 2H, J=5.94Hz),
		3.89(s, 3H), 3.69(s, 2H), 2.77(t, 2H, J=5.94Hz),
		2.53-2.49(m, 4H), 1.57-1.65(m, 4H), 1.48-1.42(m, 2H).

[0618]

TABLE 62
415	43	1 H-NMR (DMSO-d6); δ 13.56(br, 1H), 11.16(brs, 1H),	11
		8.47(d, 1H, J=8.58Hz), 8.09(s, 1H), 7.96(d, 1H, J=7.92Hz),
		7.80(d, 1H, J=8.25Hz), 7.57(dd, 1H, J=7.59, 8.25Hz),
		7.14(dd, 1H, J=7.59, 7.92Hz), 7.06-6.93(m, 5H),
		4.08(t, 2H, J=3.96Hz), 3.76(s, 2H), 3.70(t, 2H, J=3.66Hz),
		3.52(q, 2H, J=6.93Hz), 1.14(t, 3H, J=6.93Hz).
415	47	11.16(brs, 1H), 8.68(d, 1H, J=8.58Hz), 8.16(d, 1H,	10
methyl		J=2.31Hz), 8.01(dd, 1H, J=1.65, 7.92Hz), 7.71(dd, 1H,
ester		J=2.31, 8.58Hz), 7.53(ddd, 1H, J=1.65, 7.25, 8.53Hz),
		7.11-7.05(m, 3H), 6.94(d, 2H, J=8.90Hz), 6.87(d, 1H,
		J=8.58Hz), 4.12(t, 2H, J=462Hz), 3.89(s, 3H), 3.79(t,
		2H, J=4.29Hz), 3.70(s, 2H), 3.61(q, 2H, J=6.93Hz),
		1.25(t, 3H, J=6.93Hz).
416	41	1 H-NMR (DMSO-d6); δ 14.00-13.00(br, 1H), 11.20(brs,	11
		1H), 8.46(d, 1H, J=8.58Hz), 8.09(d, 1H, J=2.31Hz),
		7.95(d, 1H, J=8.25Hz), 7.80(dd, 1H, J=2.31, 8.58Hz),
		7.57(dd, 1H, J=7.59, 8.25Hz), 7.14(dd, 1H, J=7.59, 7.59Hz),
		6.91-7.07(m, 5H), 4.56-4.50(m, 1H), 3.90-3.82(m,
		2H), 3.76(s, 2H), 3.52-3.44(m, 2H), 1.99-1.94(m, 2H),
		1.66-1.52(m, 2H).
416	31	11.18(brs, 1H), 8.68(d, 1H, J=8.58Hz), 8.16(d, 1H,	10
methyl		J=2.31Hz), 8.01(dd, 1H, J=1.65, 7.92Hz), 7.72(dd, 1H,
ester		J=2.31, 8.58Hz), 7.54(ddd, 1H, J=1.65, 6.93, 8.58Hz),
		7.12-7.05(m, 3H), 6.95-6.87(m, 3H), 4.48-4.39(m, 1H),
		4.03-3.92(m, 2H), 3.90(s, 3H), 3.70(s, 2H), 3.62-3.53(m,
		2H), 2.06-1.99(m, 2H), 1.85-1.74(m, 2H).
417	68	1 H-NMR (DMSO-d6); δ 11.18(brs, 1H), 8.46(d, 1H,	11
		J=7.59Hz), 8.09(d, 1H, J=1.98Hz), 7.95(d, 1H, J=7.92Hz),
		7.80(dd, 1H, J=8.58, 1.65Hz), 7.56(dd, 1H, J=8.25,
		7.59Hz), 7.28(dd, 2H, J=7.92, 7.26Hz), 7.14(dd, 1H,
		J=7.92, 7.26Hz), 7.07-6.89(m, 8H), 4.13(t, 4H, J=6.27Hz),
		3.76(s, 2H), 2.17(m, 2H).
417	61	11.16(brs, 1H), 8.68(dd, 1H, J=8.58, 0.99Hz), 8.16(d, 1H,	10
methyl		J=2.31Hz), 8.00(dd, 1H, J=7.92, 1.65Hz), 7.70(dd, 1H,
ester		J=8.25, 2.64Hz), 7.53(ddd, 1H, J=8.58, 7.25, 1.65Hz),
		7.27(m, 2H), 7.08(m, 1H), 7.06(d, 2H, J=8.90Hz),
		6.96-6.77(m, 6H), 4.16(t, 2H, J=5.94Hz), 4.15(t, 2H,
		J=5.94Hz), 3.88(s, 3H), 3.69(s, 2H), 2.26(quint, 2H, J=5.94Hz).

[0619]

TABLE 63
418	17	1 H-NMR (DMSO-d6); δ 11.33(brs, 1H), 8.45(d, 1H,	11
	yield	J=8.57Hz), 8.08(s, 1H), 7.95(d, 1H, J=7.59Hz), 7.79(d,
	from	1H, J=8.25Hz), 7.55(dd, 1H, J=8.25, 7.58Hz), 7.12(dd,
	Ex.6	1H, J=7.59, 7.26Hz), 7.06-6.92(m, 5H), 4.05(t, 2H,
		J=4.62Hz), 3.75(s, 2H), 3.69(t, 2H, J=3.96Hz), 3.63(m,
		1H), 1.11(d, 6H, J=5.94Hz).
419	23	1 H-NMR (DMSO-d6); δ 11.19(brs, 1H), 8.46(d, 1H,	11
	yield	J=8.25Hz), 8.09(d, 1H, J=2.31Hz), 7.95(dd, 1H, J=7.92,
	from	1.65Hz), 7.80(dd, 1H, J=8.58, 1.98Hz), 7.56(dd, 1H,
	Ex.6	J=8.25, 7.26Hz), 7.13(dd, 1H, J=7.59, 7.59Hz), 7.05(d,
		2H, J=8.91Hz), 6.97(d, 2H, J=8.91Hz), 6.92(d, 1H),
		4.11(t, 2H, J=4.95Hz), 3.80(t, 2H, J=4.62Hz), 3.75(br, 6H).
420	50	1 H-NMR (DMSO-d6); δ 11.93(brs, 1H), 8.45(d, 1H,	11
		J=8.24Hz), 8.08(s, 1H), 7.96(d, 1H, J=7.92Hz), 7.79(dd,
		1H J=8.25, 1.65Hz), 7.49(dd, 1H, J=7.92, 7.92Hz),
		7.12-6.91(m, 6H), 4.06(t, 2H, J=4.29Hz), 3.74(t, 2H),
		3.72(s, 2H), 3.32(m, 1H), 1.85(m, 2H), 1.66(m, 2H), 1.21(m, 6H).
420	86	11.16(brs, 1H), 8.67(d, 1H, J=8.58Hz), 8.16(d, 1H,	10
methyl		J=2.31Hz), 8.00(dd, 1H, J=7.91, 1.65Hz), 7.71(dd, 1H,
ester		J=8.58, 2.31Hz), 7.52(ddd, 1H, J=8.58, 7.25, 1.65Hz),
		7.07(m, 1H), 7.06(d, 2H, J=8.91Hz), 6.93(d, 2H, J=9.23Hz),
		6.86(d, 1H, J=8.25Hz), 4.10(t, 2H, J=4.95Hz),
		3.89(s, 3H), 3.80(t, 2H, J=4.62Hz), 3.69(s, 2H), 3.29(m,
		1H), 1.92-1.80(m, 2H), 1.75-1.60(m, 2H), 1.34-1.20(m, 6H).
421	65	1 H-NMR (DMSO-d6); δ 11.23(brs, 1H), 8.46(d, 1H,	11
		J=8.41Hz), 8.09(s, 1H), 7.95(d, 1H, J=7.75Hz), 7.80(dd,
		1H, J=8.58, 2.64Hz), 7.56(dd, 1H, J=7.75, 7.26Hz),
		7.10(dd, 1H, J=7.75, 7.59Hz), 7.05-6.93(m, 5H), 4.36(m,
		1H), 3.75(s, 2H), 3.24(s, 3H), 3.21(m, 1H), 1.98(m, 2H),
		1.67(m, 4H), 1.42(m, 2H).
421	71	11.16(brs, 1H), 8.68(d, 1H, J=8.41Hz), 8.16(d, 1H,	10
methyl		J=2.31Hz), 8.00(dd, 1H, J=7.92, 1.65Hz), 7.71(dd, 1H,
ester		J=8.41, 2.48Hz), 7.52(ddd, 1H, J=8.74, 7.09, 1.65Hz),
		7.16-7.02(m, 3H), 6.97-6.82(m, 3H), 4.30(m, 1H), 3.88(s,
		3H), 3.69(s, 2H), 3.33(s, 3H), 3.30(m, 1H), 2.09-1.25(m, 8H).

[0620]

TABLE 64
422	43	1 H-NMR (DMSO-d6); δ 11.19(brs, 1H), 8.46(d, 1H,	11
		J=8.08Hz), 8.08(s, 1H), 7.95(dd, 1H, J=7.92, 1.65Hz),
		7.80(dd, 1H, J=8.58, 2.31Hz), 7.56(dd, 1H, J=8.58, 7.26Hz),
		7.13(dd, 1H, J=7.59, 7.59Hz), 7.07-6.92(m, 5H),
		4.08(t, 2H, J=4.45Hz), 3.76(s, 2H), 3.72(t, 2H), 3.59(t,
		2H, J=3.29Hz), 3.50(t, 2H, J=2.64Hz), 3.44(q, 2H,
		J=7.09Hz), 1.10(t, 3H, J=7.09Hz).
422	80	11.16(brs, 1H), 8.68(dd, 1H, J=8.58, 0.99Hz), 8.16(d, 1H,	10
methyl		J=2.47Hz), 8.00(dd, 1H, J=7.92, 1.65Hz), 7.71(dd, 1H,
ester		J=8.41, 2.47Hz), 7.51(ddd, 1H, J=8.58, 7.25, 1.65Hz),
		7.10-7.02(m, 3H), 6.95-6.85(m, 3H), 4.13(t, 2H, J=5.11Hz),
		3.89(s, 3H), 3.86(m, 2H), 3.71(m, 2H), 3.69(s, 2H),
		3.61(m, 2H), 3.54(q, 2H, J=6.93Hz), 1.21(t, 3H, J=6.93Hz).
423	50	1 H-NMR (DMSO-d6); δ 11.66(brs, 1H), 8.66(d, 1H,	11
		J=8.74Hz), 8.46(s, 1H), 8.01(d, 1H, J=8.24Hz), 7.91(dd,
		1H, J=8.74, 2.64Hz), 7.51(dd, 1H, J=8.90, 7.25Hz),
		7.10-6.97(m, 3H), 6.93(d, 2H, J=9.07Hz), 6.83(d, 1H,
		J=8.57Hz), 4.07(t, 2H, J=4.61Hz), 3.75(t, 2H), 3.72(s, 2H), 3.44(s, 3H).
423	86	11.15(brs, 1H), 8.67(d, 1H, J=8.57Hz), 8.16(d, 1H,	10
methyl		J=2.14Hz), 7.98(dd, 1H, J=7.92, 2.80Hz), 7.70(dd, 1H,
ester		J=8.41, 2.31Hz), 7.51(ddd, 1H, J=8.58, 7.25, 1.65Hz),
		7.09-7.05(m, 3H), 6.97-6.79(m, 3H), 4.10(dd, 2H, J=6.10,
		4.62Hz), 3.88(s, 3H), 3.73(dd, 2H, J=5.77, 4.78Hz),
		3.69(s, 2H), 3.44(s, 3H).
424	62	11.11(brs, 1H), 8.45(d, 1H, J=8.74Hz), 8.09(s, 1H),	11
		7.95(d, 1H, J=7.91Hz), 7.79(dd, 1H, J=8.57, 2.47Hz),
		7.56(dd, 1H, J=8.08, 7.75Hz), 7.13(dd, 1H, J=7.91, 6.26Hz),
		7.06-6.90(m, 5H), 4.08(t, 2H, J=4.45Hz), 3.75(s,
		2H), 3.69(t, 2H, J=3.95Hz), 3.46(t, 2H, J=6.26Hz),
		1.50(m, 2H), 1.34(m, 2H), 0.88(t, 3H, J=7.26Hz).
424	75	11.16(brs, 1H), 8.67(d, 1H, J=8.41Hz), 8.16(d, 1H,	10
methyl		J=2.47Hz), 8.00(dd, 1H, J=7.92, 1.65Hz), 7.71(dd, 1H,
ester		J=8.41, 2.31Hz), 7.52(ddd, 1H, J=8.58, 7.56, 1.65Hz),
		7.10-7.04(m, 3H), 6.93(d, 2H, J=9.07Hz), 6.87(d, 1H,
		J=8.41Hz), 4.11(t, 2H, J=4.62Hz), 3.88(s, 3H), 3.77(t,
		2H, J=4.45Hz), 3.69(s, 2H), 3.53(t, 2H, J=6.60Hz),
		1.59(m, 2H), 1.37(m, 2H), 0.92(t, 3H, J=7.26Hz).

[0621]

TABLE 65
425	76	1 H-NMR (DMSO-d6); δ 11.12(brs, 1H), 8.46(d, 1H,	11
		J=8.24Hz), 8.09(d, 1H, J=2.64Hz), 7.95(dd, 1H, J=7.91,
		1.81Hz), 7.80(dd, 1H, J=8.41, 2.63Hz), 7.57(dd, 1H,
		J=8.74, 7.25Hz), 7.13(dd, 1H, J=7.91, 7.25Hz),
		7.06-6.92(m, 5H), 4.08(t, 2H, J=4.28Hz), 3.76(s, 2H),
		3.74(t, 2H, J=4.28Hz), 3.59(t, 2H, J=3.13Hz), 3.47(t,
		2H, J=2.80Hz), 3.25(s, 3H).
425	83	11.15(brs, 1H), 8.67(d, 1H, J=8.58Hz), 8.16(d, 1H,	10
methyl		J=2.47Hz), 7.99(dd, 1H, J=7.92, 1.32Hz), 7.68(m, 1H),
ester		7.51(m, 1H), 7.28-7.01(m, 3H), 6.95-6.77(m, 3H), 4.13(t,
		2H, J=5.11Hz), 3.88(s, 3H), 3.87(t, 2H, J=5.60Hz),
		3.72(t, 2H, J=5.11Hz), 3.69(s, 2H), 3.57(t, 2H, J=5.11Hz), 3.39(s, 3H).
426	86	1 H-NMR (DMSO-d6); δ 11.19(brs, 1H), 8.45(d, 1H,	11
		J=8.57Hz), 8.08(s, 1H), 7.95(d, 1H, J=7.92Hz), 7.80(dd,
		1H, J=8.57, 2.63Hz), 7.56(dd, 1H, J=8.90, 6.76Hz),
		7.13(dd, 1H, J=7.75, 7.42Hz), 7.06-6.92(m, 5H), 4.08(t,
		2H, J=4.28Hz), 3.75(s, 2H), 3.69(t, 2H, J=3.46Hz),
		3.41(t, 2H, J=6.59Hz), 1.52(m, 2H), 0.87(t, 3H, J=7.25Hz).
426	80	11.16(brs, 1H), 8.68(d, 1H, J=8.41Hz), 8.16(d, 1H,	10
methyl		J=2.31Hz), 8.00(dd, 1H, J=7.92, 1.65Hz), 7.71(dd, 1H,
ester		J=8.41, 2.47Hz), 7.52(m, 1H), 7.10-7.03(m, 3H), 6.93(d,
		2H, J=8.91Hz), 6.87(d, 1H, J=8.41Hz), 4.11(t, 2H,
		J=5.11Hz), 3.89(s, 3H), 3.78(t, 2H, J=5.11Hz), 3.69(s,
		2H), 3.49(t, 2H, J=6.59Hz), 1.62(m, 2H), 0.93(t, 3H, J=7.42Hz).
427	79	11.69(brs, 1H), 8.46(d, 1H, J=8.4Hz), 8.11(d, 1H, J=2.2Hz),	11
		7.96(dd, 1H, J=7.8Hz), 7.77-7.87(m, 3H), 7.56(d,
		1H, J=2.4Hz), 7.52(dd, 1H, J=7.8, 7.3Hz), 7.39(d, 1H,
		J=2.4Hz), 7.27(dd, 1H, J=8.6, 2.2Hz), 7.18(dd, 1H,
		J=8.9, 2.4Hz), 7.11(dd, 1H, J=8.4, 7.3Hz), 7.04(d, 1H,
		J=8.1Hz), 4.23(t, 2H, J=5.7Hz), 3.76(s, 2H),
		3.60-3.63(m, 4H), 2.83(t, 2H, J=5.7Hz), 2.56-2.59(m, 4H).
427	56	11.17(brs, 1H), 8.69(d, 1H, J=8.6Hz), 8.17(s, 1H),	10
methyl		7.98-8.02(m, 1H), 7.64-7.76(m, 3H), 7.49-7.52(m, 2H),
ester		7.25-7.30(m, 1H), 7.07-7.17(m, 3H), 6.93-6.96(m, 1H),
		4.20-4.24(m, 2H), 3.89(s, 3H), 3.73-3.77(m, 4H), 3.71(s,
		2H), 2.84-2.88(m, 2H), 2.59-2.62(m, 4H).

[0622]

TABLE 66
428	57	10.76(brs, 1H), 8.76(d, 1H, J=7.58Hz), 8.10(dd, 1H,	11
		J=7.92, 1.65Hz), 7.59(ddd, 1H, J=8.58, 7.26, 1.65Hz),
		7.44(dd, 1H, J=1.98, 0.99Hz), 7.29(d, 2H, J=8.58Hz),
		7.09(ddd, 1H, J=7.91, 7.26, 0.99Hz), 6.98(d, 2H, J=8.58Hz),
		6.94-6.84(m, 4H), 6.42-6.37(m, 2H), 4.93(s, 2H), 3.76(s, 2H).
428	35	11.03(brs, 1H), 8.71(d, 1H, J=8.25Hz), 7.99(dd, 1H,	10
methyl		J=7.91, 1.65Hz), 7.52(ddd, 1H, J=8.58, 7.25, 1.65Hz),
ester		7.45(dd, 1H, J=1.65, 0.66Hz), 7.31(d, 2H, J=8.58Hz),
		7.06(dd, 1H, J=7.26, 6.92Hz), 7.01-6.87(m, 6H),
		6.43-6.37(m, 2H), 4.98(s, 2H), 3.87(s, 3H), 3.73(s, 2H).
981	75	13.51(br, 1H), 11.16(brs, 1H), 9.31(brs, 1H), 8.47(d, 1H,	11
		J=7.6Hz), 8.08(s, 1H), 7.95(d, 1H, J=7.9Hz), 7.77(d, 1H,
		J=8.6Hz), 7.56(t, 1H, J=7.9Hz), 7.13(t, 1H, J=7.9Hz),
		6.94-6.87(m, 3H), 6.77(d, 2H, J=8.9Hz), 3.75(s, 2H).
982	30	11.77(brs, 1H), 8.66(d, 1H, J=8.3Hz), 8.51(s, 1H), 8.02(d,	11
		1H, J=7.9Hz), 7.94(d, 1H, J=8.9Hz), 7.51(t, 1H, J=7.1Hz),
		7.01-7.09(m, 3H), 6.83-6.88(m, 3H), 4.68(brm, 1H),
		3.73(s, 2H), 1.4-2.0(brm, 8H).
983	41	1 H-NMR (DMSO-d6); δ 11.27(brs, 1H), 8.55(d, 1H,	11
		J=8.25Hz), 8.18(d, 1H, J=1.98Hz), 8.04(dd, 1H, J=1.32,
		7.92Hz), 7.89(dd, 1H, J=2.31, 8.25Hz), 7.66(ddd, 1H,
		J=1.32, 6.92, 8.58Hz), 7.23(dd, 1H, J=6.93, 7.59Hz),
		7.12(d, 2H, J=9.24Hz), 7.03(d, 1H, J=8.24Hz), 6.99(d,
		2H, J=8.91Hz), 4.53(m, 1H), 3.85(s, 2H), 2.01-1.50(m, 14H).
984	38	1 H-NMR (DMSO-d6); δ 13.66(br, 1H), 11.27(brs, 1H),	11
		8.55(d, 1H, J=8.25Hz), 8.18(d, 1H, J=2.31Hz), 8.05(dd,
		1H, J=1.32, 7.92Hz), 7.89(dd, 1H, J=2.31, 8.25Hz),
		7.66(dd, 1H, J=6.93, 7.25Hz), 7.23(t, 1H, J=7.26Hz),
		7.12(d, 2H, J=8.91Hz), 7.04(d, 1H, J=8.57Hz), 7.03(d,
		2H, J=8.80Hz), 4.25(m, 1H), 3.85(s, 2H), 1.70(m, 4H), 1.00(t, 6H, J=7.26Hz).
985	35	1 H-NMR (DMSO-d6); δ 14.15(brs, 1H), 8.40(d, 1H,	11
		J=7.92Hz), 8.05(d, 1H, J=1.98Hz), 8.00(d, 1H, J=7.59Hz),
		7.77(dd, 1H, J=2.31, 8.58Hz), 7.27(dd, 1H, J=7.26,
		7.92Hz), 7.02-6.89(m, 6H), 4.27(m, 1H), 3.60(s, 2H),
		1.89(m, 2H), 1.72(m, 2H), 1.53-1.23(m, 6H).

[0623]

TABLE 67
987	23	11.64(brs, 1H), 8.65(d, 1H, J=8.6Hz), 8.45(s, 1H), 8.04(d,	11
		1H, J=7.9Hz), 7.91(d, 1H, J=8.6Hz), 7.51(t, 1H, J=7.6Hz),
		7.06(m, 1H), 7.03(d, 2H, J=8.9Hz), 6.90-6.82(m,
		3H), 3.86(m, 1H), 3.74(s, 2H), 1.80-1.60(brm, 4H), 1.55-1.20(br, 18H).
990	86	11.72(brs, 1H), 8.66(d, 1H, J=8.3Hz), 8.48(d, 1H, J=2.0Hz),	11
		8.01(dd, 1H, J=1.3, 7.9Hz), 7.93(dd, 1H, J=2.3, 8.6Hz),
		7.51(dt, 1H, J=1.3, 7.9Hz), 7.03-7.07(m, 1H),
		7.04(d, 2H, J=9.2Hz), 6.89(d, 2H, J=8.9Hz), 6.83(d, 1H,
		J=8.6Hz), 5.19(t, 1H, J=7.1Hz), 3.88(t, 2H, J=7.1Hz),
		3.73(s, 2H), 2.46(q, 2H, J=6.9Hz), 1.73(s, 3H), 1.66(s, 3H).
991	97	11.71(brs, 1H), 8.66(d, 1H, J=8.6Hz), 8.48(s, 1H), 8.01(d,	11
		1H, J=1.6, 7.9Hz), 7.93(dd, 1H, J=2.3, 8.6Hz), 7.51(t,
		1H, J=7.2Hz), 7.09-7.06(m, 1H), 7.05(d, 2H, J=8.9Hz),
		6.92(d, 2H, J=9.2Hz), 6.85(d, 1H, J=8.6Hz),
		6.10-5.96(m, 1H), 5.40(m, 1H), 5.28(m, 1H), 4.48(dd, 2H,
		J=1.3, 4.8Hz), 3.73(s, 2H).
992	69	11.68(sbr, 1H), 8.66(d, 1H, J=8.3Hz), 8.48(d, 1H, J=2.3Hz),	11
		8.01(d, 1H, J=7.9Hz), 7.92(dd, 1H, J=2.6, 8.6Hz),
		7.51(t, 1H, J=7.2Hz), 7.06(m, 1H), 7.04(d, 2H, J=8.9Hz),
		6.90(d, 2H, J=9.2Hz), 6.84(d, 1H, J=8.6Hz),
		5.67-5.89(m, 2H), 4.40(d, 2H, J=5.9Hz), 3.73(s, 2H), 1.75(d, 3H, J=6.3Hz).
993	42	11.71(brs, 1H), 8.66(d, 1H, J=8.3Hz), 8.49(d, 1H, J=2.0Hz),	11
		8.01(dd, 1H, J=1.7, 7.9Hz), 7.93(dd, 1H, J=2.0, 8.6Hz),
		7.50(t, 1H, J=7.6Hz), 7.09-7.06(m, 1H), 7.04(d, 2H,
		J=9.2Hz), 6.92(d, 2H, J=9.2Hz), 6.84(d, 1H, J=8.6Hz),
		5.08(s, 1H), 4.98(s, 1H, 4.38(s, 2H), 3.73(s, 2H), 1.81(s, 3H).
994	86	11.70(brs, 1H), 8.65(d, 1H, J=8.3Hz), 8.48(d, 1H, J=2.0Hz),	11
		8.03(d, 1H, J=7.9Hz), 7.91(dd, 1H, J=2.3, 8.6Hz),
		7.51(t, 1H, J=7.2Hz), 7.06-7.00(m, 1H), 7.01(d, 2H,
		J=8.3Hz), 6.91(d, 2H, J=9.2Hz), 6.83(d, 1H, J=8.6Hz),
		5.47(t, 1H, J=6.2Hz), 5.09(t, 1H, J=6.2Hz), 4.49(d, 2H,
		J=6.2Hz), 3.73(s, 2H), 2.09(brm, 4H), 1.71(s, 3H), 1.68(s, 3H), 1.60(s, 3H).
1002	10	11.67(brs, 1H), 8.66(d, 1H, J=8.6Hz), 8.45(s, 1H),	11
		8.02(dd, 1H, J=1.3, 7.9Hz), 7.91(dd, 1H, J=2.0, 8.6Hz),
		7.54(t, 1H, J=7.2Hz), 7.09-6.82(m, 6H), 6.40-6.32(m,
		1H), 5.97-5.84(m, 2H), 5.37-5.05(m, 3H), 4.52(d, J=4.3Hz,
		1H), 3.72(s, 2H).

[0624]

TABLE 68
1017	60	1 H-NMR (DMSO-d6); δ 13.56(br, 1H), 11.18(brs, 1H),	11
		8.46(d, 1H, J=8.57Hz), 8.08(s, 1H), 7.95(d, 1H, J=7.92Hz),
		7.79(d, 1H, J=8.25Hz), 7.57(dd, 1H, J=7.26, 8.58Hz),
		7.37(m, 2H), 7.16-6.92(m, 8H), 4.17(t, 2H, J=6.60Hz), 3.76(s, 2H), 3.03(t, 2H,
		J=6.60Hz).
1019	34	1 H-NMR (DMSO-d6); δ 14.26(br, 1H), 8.40(d, 1H,	11
		J=7.92Hz), 8.19(d, 2H, J=7.26Hz), 8.05(s, 1H), 8.00(d,
		1H, J=7.58Hz), 7.78(d, 1H, J=6.27Hz), 7.64(d, 2H,
		J=7.92Hz), 7.26(dd, 1H, J=6.93, 8.25Hz), 7.04-6.85(m,
		5H), 6.77(d, 1H, J=7.91Hz), 4.26(t, 2H, J=6.6Hz), 3.61(s, 2H), 3.20(t, 2H,
		J=6.27Hz).
1021	82	13.56(br, 1H), 11.18(brs, 1H), 8.46(d, 1H, J=7.58Hz),	11
		8.08(d, 1H, J=1.98Hz), 7.95(d, 1H, J=7.92Hz), 7.80(dd,
		1H, J=1.98, 8.58Hz), 7.57(dd, 1H, J=7.59, 8.25Hz),
		7.33-7.21(m, 5H), 7.13(dd, 1H, J=7.26, 7.92Hz),
		7.06-6.92(m, 5H), 4.19(t, 2H, J=6.93Hz), 3.75(s, 2H), 3.04(t, 2H,
		J=6.93Hz).
1059	35	1 H-NMR (DMSO-d6); δ 8.81(d, 1H, J=1.65Hz), 8.70(d,	11
		1H, J=7.91Hz), 8.43(dd, 1H, J=1.31, 8.24Hz), 8.14(d,
		1H, J=7.59Hz), 7.53(m, 1H), 7.23-7.14(m, 4H), 7.06(d,
		2H, J=9.24Hz), 4.30(m, 1H), 1.72(m, 4H), 1.02(t, 6H, J=7.26Hz).
1060	35	1 H-NMR (DMSO-d6); δ 8.80(d, 1H, J=2.31Hz), 8.71(d,	11
		1H, J=8.57Hz), 8.41(dd, 1H, J=2.31, 8.57Hz), 8.14(d,
		1H, J=8.58Hz), 7.64(dd, 1H, J=7.59, 7.91Hz),
		7.27-7.10(m, 4H), 7.07(d, 2H, J=9.24Hz), 4.40(m, 1H), 2.08-1.36(m, 10H).
1061	25	1 H-NMR (DMSO-d6); δ 12.28(br, 1H), 8.78(d, 1H,	11
		J=2.31Hz), 8.71(d, 1H, J=8.57Hz), 8.39(dd, 1H, J=2.96,
		8.58Hz), 8.14(dd, 1H, J=1.65, 7.92Hz), 7.75(dd, 1H,
		J=7.26, 8.25Hz), 7.31(dd, 1H, J=6.60, 7.59Hz), 7.24(d,
		1H, J=8.58Hz), 7.20(d, 2H, J=8.90Hz), 7.03(d, 2H,
		J=9.23Hz), 4.56(m, 1H), 2.00-1.55(m, 14H).
1077	100	11.16(brs, 1H), 8.69(d, 1H, J=8.58Hz), 8.18(d, 1H,	10
		J=2.31Hz), 8.01(dd, 1H, J=1.65, 7.92Hz), 7.72(dd, 1H,
		J=2.31, 8.58Hz), 7.53(ddd, 1H, J=1.65, 7.26, 8.57Hz),
		7.11-6.98(m, 3H), 6.92-6.86(m, 3H), 4.10(m, 1H), 3.89(s,
		3H), 3.71(s, 2H), 1.68(m, 4H), 0.96(t, 6H, J=7.25Hz).

[0625]

TABLE 69
1079	89	11.16(brs, 1H), 8.69(d, 1H, J=8.3Hz), 8.17(d, 1H, J=2.3Hz),	10
		8.00(dd, 1H, J=1.7, 7.9Hz), 7.70(dd, 1H, J=2.3, 8.9Hz),
		7.50(t, 1H, J=7.1Hz), 7.06-7.10(m, 1H), 7.05(d, 2H,
		J=8.9Hz), 6.85-6.90(m, 3H), 4.72(brm, 1H), 3.89(s, 3H),
		3.70(s, 2H), 1.8-2.0(brm, 4H), 1.5-1.75(brm, 4H).
1080	85	11.16(brs, 1H), 8.68(d, 1H, J=8.25Hz), 8.17(d, 1H,	10
		J=2.64Hz), 8.01(dd, 1H, J=1.65, 8.25Hz), 7.71(dd, 1H,
		J=2.31, 8.58Hz), 7.53(ddd, 1H, J=1.65, 7.25, 8.58Hz),
		7.27-7.02(m, 3H), 6.93-6.86(m, 3H), 3.97(m, 1H), 3.89(s, 3H), 3.70(s, 2H),
		2.04-1.05(m, 10H).
1081	100	11.16(brs, 1H), 8.68(d, 1H, J=8.58Hz), 8.17(d, 1H,	10
		J=2.31Hz), 8.01(dd, 1H, J=1.65, 7.92Hz), 7.71(dd, 1H,
		J=2.31, 8.58Hz), 7.53(ddd, 1H, J=1.65, 7.26, 8.57Hz),
		7.11-7.03(m, 3H), 6.88-6.84(m, 3H), 4.36(m, 1H), 3.89(s, 3H),
		3.70(s, 2H), 2.01-1.54(m, 14H).
1082	92	11.16(brs, 1H), 8.68(d, 1H, J=8.6Hz), 8.17(d, 1H, J=2.4Hz),	10
		8.00(d, 1H, J=7.9Hz), 7.71(dd, 1H, J=2.3, 8.6Hz),
		7.53(t, 1H, J=7.3Hz), 7.10-7.03(m, 3H), 6.92-6.86(m,
		3H), 3.89(s, 3H), 3.84(m, 1H), 3.70(s, 2H), 1.80-1.60(brm, 4H),
		1.55-1.20(br, 18H).
1083	33	11.16(brs, 1H), 8.68(d, 1H, J=8.58Hz), 8.16(d, 1H,	10
		J=2.31Hz), 8.01(dd, 1H, J=1.65, 7.92Hz), 7.71(dd 1H,
		J=2.64, 8.58Hz), 7.53(ddd, 1H, J=1.65, 7.26, 8.57Hz),
		7.11-7.04(m, 3H), 6.93-6.86(m, 3H), 3.89(s, 3H), 3.81(dd,
		2H, J=5.61, 10.23Hz), 3.70(s, 2H), 1.56-1.23(m, 7H), 1.03-0.84(m, 6H).
1084	38	11.16(brs, 1H), 8.68(d, 1H, J=8.6Hz), 8.16(d, 1H, J=2.3Hz),	6
		8.00(d, 1H, J=1.6, 7.9Hz), 7.71(dd, 1H, J=2.3, 8.6Hz),
		7.52(t, 1H, J=7.2Hz), 7.11-7.05(m, 3H), 6.92(d, 2H,
		J=6.9Hz), 6.88(d, 1H, J=8.6Hz), 6.11-5.99(m, 1H),
		5.46-5.37(m, 1H), 5.32-5.26(m, 1H), 4.52(d, 2H, J=5.9Hz), 3.89(s, 3H),
		3.69(s, 2H).

[0626]

TABLE 70
1085	34	11.17(brs, 1H), 8.68(d, 1H, J=8.6Hz), 8.16(d, 1, J=2.3Hz,	6
		H), 8.00(dd, 1H, J=1.6, 7.9Hz), 7.70(dd, 1H, J=2.3,
		8.6Hz), 7.53(dt, 1H, J=1.3, 7.9Hz), 7.10-7.06(m, 1H),
		7.06(d, 2H, J=9.2Hz), 6.90(d, 2H, J=8.9Hz),
		6.89-6.85(m, 1H), 5.21(t, 1H, J=7.1Hz), 3.92(t, 2H, J=7.1Hz),
		3.89(s, 3H), 3.70(s, 2H), 2.46(q, 2H, J=6.9Hz), 1.73(s, 3H), 1.66(s, 3H).
1086	39	11.17(brs, 1H), 8.68(d, 1H, J=8.6Hz), 8.16(s, 1H, 8.00(d,	10
		1H, J=7.1Hz), 7.71(d, 1H, J=8.3Hz), 7.53(t, 1H, J=7.1Hz),
		7.11-7.03(m, 3H), 6.96-6.85(m, 3H), 6.0-5.8(m, 2H),
		5.4-5.1(m, 4H), 4.56(d, 1H, J=5.6Hz), 3.89(s, 3H), 3.70(s, 2H).
1087	41	11.16(brs, 1H, 8.68(d, 1H, J=8.6Hz), 8.16(d, 1H, J=2.3Hz),	10
		8.00(dd, 1H, J=1.6, 7.9Hz), 7.71(dd, 1H, J=2.3, 8.6Hz),
		7.53(t, 1H, J=7.8Hz), 7.11-7.06(m, 1H), 7.06(d, 2H,
		J=9.2Hz), 6.91(d, 2H, J=8.9Hz), 6.88(d, 1H, J=8.3Hz),
		5.91-5.70(m, 2H), 4.44(d, 2H, J=5.6Hz), 3.89(s, 3H), 3.70(s, 2H),
		1.76(dd, 3H, J=1.0, 5.3Hz).
1088	42	11.16(brs, 1H), 8.68(d, 1H, J=8.6Hz), 8.16(d, 1H, J=2.3Hz),	10
		8.00(dd, 1H, J=1.6, 7.9Hz), 7.71(dd, 1H, J=2.3, 8.6Hz),
		7.52(dt, 1H, J=1.6, 7.9Hz), 7.10-7.04(m, 3H),
		6.93(d, 2H, J=8.9Hz), 6.88(d, 1H, J=8.6Hz), 5.10(s, 1H),
		4.99(s, 1H), 4.42(s, 2H), 3.89(s, 3H), 3.70(s, 2H), 1.83(s, 3H).
1089	23	11.16(brs, 1H), 8.68(d, 1H, J=8.6Hz), 8.16(d, 1H, J=2.3Hz),	6
		8.00(d, 1H, J=7.9Hz), 7.71(d, 1H, J=2.3, 8.6Hz),
		7.52(t, 1H, J=7.9Hz), 7.08-7.11(m, 1H), 7.06(d, 2H,
		J=8.9Hz), 6.92(d, 2H, J=8.9Hz), 6.88(d, 1H, J=8.3Hz),
		5.50(t, 1H, J=6.3Hz), 5.09(br, 1H), 4.52(d, 2H, J=6.6Hz),
		3.89(s, 3H), 3.70(s, 2H), 2.05(brm, 4H), 1.73(s, 3H), 1.68(s, 3H), 1.60(s, 3H).
1090	49	11.16(brs, 1H), 8.68(d, 1H, J=8.25Hz), 8.16(d, 1H,	10
		J=2.31Hz), 8.01(dd, 1H, J=1.65, 7.92Hz), 7.71(dd, 1H,
		J=2.31, 8.58Hz), 7.53(ddd, 1H, J=1.65, 7.26, 8.57Hz),
		7.35-7.21(m, 5H), 7.11-7.04(m, 3H), 6.93-6.86(m, 3H),
		4.17(t, 2H, J=6.92Hz), 3.89(s, 3H), 3.70(s, 2H), 3.10(t, 2H, J=6.92Hz).

[0627]

TABLE 71
1091	61	11.17(brs, 1H), 8.68(d, 1H, J=8.58Hz), 8.15(d, 1H,	10
		J=2.31Hz), 8.01(dd, 1H, J=1.65, 7.92Hz), 7.71(dd, 1H,
		J=2.31, 8.58Hz), 7.53(ddd, 1H, J=1.32, 7.26, 8.57Hz),
		7.25(m, 2H), 7.10-6.86(m, 8H), 4.14(t, 2H, J=6.93Hz),
		3.89(s, 3H) 3.69(s, 2H), 3.06(t, 2H, J=6.93Hz).
1101	92	12.07(s, 1H), 8.90(d, 1H, J=2.63Hz), 8.88(d, 1H, J=8.25Hz),	10
		8.32(dd, 1H, J=2.64, 8.58Hz), 8.08(dd, 1H, J=1.65,
		7.92Hz), 7.60(ddd, 1H, J=1.65, 7.26, 8.58Hz),
		7.16-6.93(m, 6H), 4.22(m, 1H), 3.94(s, 3H), 2.04-1.26(m, 10H).
1102	89	12.07(brs, 1H), 8.90(d, 1H, J=2.63Hz), 8.88(dd, 1H,	10
		J=0.66, 8.58Hz), 8.31(dd, 1H, J=2.30, 8.57Hz), 8.07(dd,
		1H, J=1.32, 7.92Hz), 7.60(ddd, 1H, J=1.32, 7.26, 8.58Hz),
		7.15-7.06(m, 3H), 6.99(d, 1H, J=8.91), 6.90(d, 2H, J=8.91Hz),
		4.39(m, 1H), 3.94(s, 3H), 2.04-1.41(m, 14H).
1103	65	12.08(brs, 1H), 8.90(d, 1H, J=2.63Hz), 8.88(dd, 1H,	10
		J=0.66, 8.91Hz), 8.32(dd, 1H, J=2.65, 8.58Hz), 8.08(dd,
		1H, J=1.65, 7.92Hz), 7.60(ddd, 1H, J=1.65, 7.26, 8.58Hz),
		7.16-6.91(m, 6H), 4.09(m, 1H), 3.94(s, 3H), 1.70(m, 4H), 0.98(t, 6H,
		J=7.25Hz).
1105	100	11.16(brs, 1H), 8.69(d, 1H, J=8.58Hz), 8.18(d, 1H,	10
		J=2.31Hz), 8.01(dd, 1H, J=1.65, 7.92Hz), 7.72(dd, 1H,
		J=2.31, 8.58Hz), 7.53(ddd, 1H, J=1.65, 7.26, 8.57Hz),
		7.11-6.98(m, 3H), 6.92-6.86(m, 3H), 4.10(m, 1H), 3.89(s,
		3H), 3.71(s, 2H), 1.68(m, 4H), 0.96(t, 6H, J=7.25Hz).
1108	30	11.16(brs, 1H), 8.67(d, 1H, J=8.25Hz), 8.15(d, 1H,	10
		J=2.31Hz), 7.99(dd, 1H, J=1.32, 7.91Hz), 7.71(dd, 1H,
		J=2.31, 8.25Hz), 7.51(ddd, 1H, J=1.32, 7.25, 8.57Hz),
		7.10-7.03(m, 3H), 6.94-6.87(m, 3H), 4.26(t, 2H, J=6.27Hz), 3.88(s, 3H),
		3.69(s, 2H), 3.62(t, 2H, J=6.27Hz).
1118	60	1 H-NMR (DMSO-d6); δ 0.93(6H, t, J=7.81Hz), 1.67(4H,	11
		dq, J=5.86, 7.81Hz), 3.77(2H, s), 4.37(1H, tt, J=5.86,
		5.86Hz), 7.03(1H, d, J=7.81Hz), 7.15(2H, m), 7.25(1H,
		m), 7.35(1H, s), 7.54(1H, s), 7.57(1H, dd, J=7.81, 7.81Hz),
		7.76(1H, d, J=9.76Hz), 7.83(2H, m), 7.95(1H, d,
		J=7.81Hz), 8.11(1H, s), 8.45(1H, d, J=9.76Hz), 11.13(1H, s), 13.56(1H, br).

[0628]

TABLE 72
1205	35	1.00(6H, t, J=7.51Hz), 1.74(4H, m), 3.71(2H, s), 3.90(3H,	10
		s), 4.21(1H, m), 6.94(1H, d, J=6.94Hz), 7.11(3H, m),
		7.26(1H, m), 7.50(2H, m), 7.70(3H, m), 8.02(1H, dd,
		J=1.73, 8.00Hz), 8.18(1H, d, J=2.47Hz), 8.69(1H, dd, J=0.91, 8.50Hz),
		11.19(1H, s).
1243	41	11.16(brs, 1H), 8.68(d, 1H, J=8.6Hz), 8.16(d, 1H, J=2.3Hz),	10
		8.00(dd, 1H, J=1.6, 7.9Hz), 7.71(dd, 1H, J=2.3, 8.6Hz),
		7.53(t, 1H, J=7.8Hz), 7.11-7.06(m, 1H), 7.06(d, 2H,
		J=9.2Hz), 6.91(d, 2H, J=8.9Hz), 6.88(d, 1H, J=8.3Hz),
		5.91-5.70(m, 2H), 4.44(d, 2H, J=5.6Hz), 3.89(s, 3H), 3.70(s, 2H),
		1.76(dd, 3H, J=1.0, 5.3Hz).
1244	55	1 H-NMR (DMSO-d6); δ 14.25(brs, 1H), 8.41(d, 1H,	11
		J=8.25Hz), 8.06(s, 1H), 8.00(d, 1H, J=7.91), 7.78(d, 1H,
		J=8.58Hz), 7.27(dd, 1H, J=7.26, 8.25Hz), 7.05-6.90(m,
		6H), 3.83(dd, 2H, J=6.27, 10.23Hz), 3.61(s, 2H), 1.47-1.28(m, 7H),
		1.00-0.89(m, 6H).
1245	41	1 H-NMR (DMSO-d6); δ 14.00-13.00(br, 1H), 11.20(brs,	11
		1H), 8.46(d, 1H, J=8.58Hz), 8.09(d, 1H, J=2.31Hz),
		7.95(d, 1H, J=8.25Hz), 7.80(dd, 1H, J=2.31, 8.58Hz),
		7.57(dd, 1H, J=7.59, 8.25Hz), 7.14(dd, 1H, J=7.59, 7.59Hz),
		6.91-7.07(m, 5H), 4.56-4.50(m, 1H), 3.90-3.82(m,
		2H), 3.76(s, 2H), 3.52-3.44(m, 2H), 1.99-1.94(m, 2H), 1.65-1.52(m, 2H).
Note:
In the above tables, “methyl ester” means the carboxylic acid ester at the anthranilic acid site, and “methyl ester” and “ethyl ester” shown in the lower column mean carboxylic acid esters at the other site.

[0629]

TABLE 73
Compound		Measured value	Yield of	Yield of
No.	M	(M + 1)+	Example 10	Example 11
80	461.18	462.2	100	100
81	503.23	504.2	24	46
82	475.2	476.2	27	100
83	529.25	530.2	11	100
84	475.2	476.2	4	100
85	489.22	490.2	39	100

[0630]

TABLE 74
Compound		Measured value	Yield of	Yield of
No.	M	(M + 1)+	Example 6	Example 8
88	513.18	514.2	48	76

[0631]

TABLE 75
					Yield
					(%)
Com-		Measured	Acylation	Hydrolysis	1st and	Exam-
pound		value	yield (%)	yield (%)	2nd	ple
No.	M	(M + 1)+	1st stage	2nd stage	stages	No.
52	474.18	475.2	73	100	73	25
53	490.17	491.2	87	100	87	25
54	536.19	537.4	84	100	84	25
55	474.18	475.2	67	100	67	25
56	490.17	491.2	55	100	55	25
57	536.19	537.4	58	100	58	25
58	488.19	489	73	91	66	25
59	504.19	505	75	88	66	25
60	550.21	551	30	44	13	25
61	488.19	489	56	58	29	25
62	504.19	505	61	77	47	25
63	550.21	551	82	81	66	25
64	502.21	503	65	63	41	25
65	564.23	565	76	52	40	25
66	518.21	519	56	65	36	25
67	502.21	503	41	84	34	25
68	564.23	565	87	85	74	25
69	518.21	519	71	77	55	25
70	502.21	503	59	96	56	25
71	564.23	565	72	88	63	25
72	518.21	519	78	99	77	25

[0632]

TABLE 76
73	502.21	503	51	91	46	25
74	564.23	565	70	94	66	25
75	518.21	519	71	61	43	25
76	488.19	489.2	70	100	70	25
77	550.21	551.2	45	100	45	25
78	488.19	489.2	61	100	61	24
79	504.19	505.2	59	100	59	25
95	502.21	503.3	78	51	39	21
96	564.23	565.3	100	50	51	20
97	578.24	579.3	100	63	63	21
98	594.24	595.3	100	65	65	21
99	598.19	599.3	99	46	45	21
100	632.52	633.3	100	60	60	21
101	565.22	566.3	82	45	37	21
102	565.22	566.3	56	22	13	21
103	516.23	517.3	72	32	23	21
104	530.24	531.3	70	57	40	21
105	560.24	531.3	79	63	50	21
106	544.26	545.3	98	77	76	21
107	544.26	545.3	84	47	40	21
108	544.26	545.3	89	63	56	21
109	586.3	587.3	94	94	89	21

[0633]

TABLE 77
110	570.27	571.3	83	76	64	21
111	609.21	610.3	100	32	32	21
112	578.24	579.3	78	45	35	21
113	594.24	595.3	86	94	81	21
114	592.26	593.3	89	60	53	21
115	554.21	555.0	96	51	49	21
116	567.2	568.3	26	27	7	21
117	538.18	539.3	96	63	61	21
118	552.19	553.3	88	54	48	21
119	566.21	567.3	90	43	39	21
120	580.22	581.3	68	50	34	21
121	600.19	601.3	100	63	63	21
122	614.21	615.3	88	68	61	21
123	634.15	635.3	92	65	60	21
124	668.12	669.3	93	52	49	21
125	645.18	646.3	96	2	2	21
126	614.21	615.3	34	13	5	21
127	518.21	519.3	30	71	21	21
128	532.22	533.3	62	48	30	21
129	546.24	547.3	38	14	5	21
130	546.24	547.3	31	61	19	21
131	560.25	561.3	49	45	22	21
132	560.25	561.3	14	16	2	21

[0634]

TABLE 78
133	560.25	561.3	35	49	17	21
134	594.24	595.3	41	65	27	21
135	573.25	574.3	27	72	20	21
136	545.25	546.3	45	69	31	21
137	545.25	546.3	32	67	22	21
138	579.24	580.3	19	69	13	21
139	593.25	594.3	6	99	6	21
140	609.25	610.3	13	79	11	21
141	613.2	614.3	19	89	17	21
142	647.16	648.3	27	61	17	21
143	624.22	625.3	21	60	13	21
144	593.25	594.3	34	95	32	21
145	629.25	630.3	40	62	25	21
146	579.24	580.3	78	54	42	23
147	593.25	594.3	72	60	43	23
148	607.27	608.3	67	50	34	23
149	588.17	589.3	88	61	54	23
150	553.22	554.3	78	88	69	23
151	580.22	581.3	69	61	42	23
152	580.22	581.3	98	61	60	23
153	580.22	581.3	87	77	67	23
154	579.24	580.3	83	40	33	23
155	579.24	580.3	76	73	55	23

[0635]

TABLE 79
156	593.25	594.3	78	69	54	23
157	607.27	608.3	79	34	27	23
158	607.27	608.3	70	60	42	23
159	621.25	622.3	100	66	66	23
160	621.25	622.3	100	59	59	23
161	606.24	607.3	89	72	64	23
162	610.21	611.3	81	73	59	23
163	622.13	623.3	100	54	54	23
164	604.22	605.3	88	62	55	23
165	567.24	568.3	61	57	35	23
166	603.24	604.3	100	62	62	23
167	617.25	618.3	71	57	40	23
168	603.24	604.3	46	17	8	23
169	603.24	604.3	71	74	53	23
170	603.24	604.3	67	53	36	23
171	554.22	555	74	74	55	23
172	604.24	605.3	85	56	48	23
173	605.23	606.3	34	66	22	23
174	604.14	605	81	64	52	23
175	578.24	579.3	—	—	14	21
176	578.24	579.3	57	71	40	21
177	594.24	595.3	31	55	17	21
178	608.22	609.3	29	63	18	21

[0636]

TABLE 80
179	582.22	583.3	43	62	27	21
180	582.22	583.3	59	75	44	21
181	598.19	599.3	43	73	31	21
182	598.19	599.3	61	85	52	21
183	642.16	645.3	63	62	39	21
184	632.21	633.3	69	49	34	21
185	632.21	633.3	66	64	42	21
186	648.21	649.3	59	61	36	21
187	648.21	649.3	46	62	29	21
188	648.21	649.3	48	37	18	21
189	608.64	609	54	60	32	21
190	589.22	590.3	29	77	22	21
191	589.22	590.3	22	46	10	21
192	640.26	641.3	53	71	38	21
193	614.24	615.3	47	72	34	21
194	614.24	615.3	43	68	29	21
195	632.15	633	53	75	40	21
196	599.18	600	17	89	15	21
197	570.18	571	43	65	28	21
198	620.20	621.3	50	69	35	21
199	528.23	529	57	85	48	21
200	528.23	529.3	20	77	15	21
201	542.24	543.3	27	66	18	21

[0637]

TABLE 81
202	614.21	615.3	44	65	29	21
203	614.21	615.3	41	69	28	21
204	660.21	661.3	36	72	26	21
205	660.21	661.3	35	73	26	21
206	618.18	619.3	46	59	27	21
207	618.18	619.3	43	78	33	21
208	618.18	619.3	39	69	27	21
209	634.15	635	42	65	27	21
210	634.15	635	43	45	19	21
211	678.12	681	47	56	26	21
212	668.18	669.3	46	80	37	21
213	668.18	669.3	41	81	33	21
214	668.18	669.3	47	37	17	21
215	684.18	685	63	39	25	21
216	614.21	626.3	46	85	39	21
217	625.19	626.3	86	14	12	21
218	678.17	679.3	24	6	1	21
219	593.25	594.3	23	42	10	21
220	593.25	594.3	38	6	2	21
221	597.23	598.3	47	58	27	21
222	597.23	598.3	31	36	11	21
223	597.23	598.3	18	46	8	21
224	613.2	614.3	48	71	34	21

[0638]

TABLE 82
225	613.2	614.3	29	66	19	21
226	657.17	660	19	44	8	21
227	609.25	610.3	38	38	14	21
228	609.25	610.3	20	71	14	21
229	647.22	648.3	57	34	19	21
230	647.22	648.3	48	28	13	21
231	663.22	664.3	49	29	14	21
232	663.22	664.3	39	37	14	21
233	604.23	605	7	15	1	21
234	625.22	626.3	35	18	6	21
235	625.22	626.3	—	—	23	21
236	621.25	622.3	12	66	8	21
237	621.25	622.3	10	71	7	21
238	632.21	633.3	39	80	31	21
239	514.21	515.3	—	—	7	21
240	599.18	600.3	35	20	7	21
241	633.14	630.3	40	100	40	21
242	633.14	630.3	50	54	27	21
243	611.21	612.3	19	43	8	21
244	657.25	658.3	58	69	40	21
245	667.22	664.3	73	45	33	21
246	599.18	600.3	11	100	11	21
247	613.2	614.3	35	97	34	21

[0639]

TABLE 83
248	714.15	715	77	86	66	21
249	638.1	639	77	83	64	21
250	648.15	649.3	20	59	12	21
251	633.14	634	100	58	58	21
252	629.19	630.3	97	57	55	21
254	565.22	566.3	100	90	90	22
255	618.13	619.3	90	88	79	21
256	586.18	587.3	68	95	65	21
257	654.1	655	66	84	55	21
258	633.14	634.3	83	87	72	21
259	646.2	647.3	76	82	62	21
260	604.17	605.3	78	92	72	21
261	604.17	605.3	74	87	64	21
262	654.16	655.3	81	91	74	21
263	670.16	671.3	79	91	72	21
264	611.17	612.3	86	85	73	21
265	579.24	580.3	100	96	96	21
266	603.24	604.3	100	82	82	21
267	632.15	633.3	100	88	88	21
268	600.19	601.3	91	99	90	21
269	668.12	669.3	91	86	78	21
270	647.16	648.3	88	88	77	21
271	660.21	661.3	92	84	77	21

[0640]

TABLE 84
272	618.18	619.3	85	89	76	21
273	618.18	619.3	81	86	70	21
274	668.18	669.3	95	86	82	21
275	684.18	685.3	87	92	80	21
276	625.19	626.3	92	87	80	21
277	593.25	594.3	100	94	94	23
278	617.25	618.3	100	98	98	23
279	564.23	565.3	99	76	75	21
280	584.17	585.3	100	88	88	21
281	618.13	619.3	100	86	86	21
282	580.22	581.3	69	80	55	21
283	572.29	573.3	100	80	80	21
284	580.22	581.3	100	85	85	21
285	551.21	552.3	71	64	45	21
286	551.21	552.3	72	65	47	21
287	516.23	517.3	45	60	27	21
288	530.24	531.3	39	59	23	21
289	530.24	531.3	—	—	68	21
290	628.14	631.3	100	75	75	21
291	618.2	619.3	100	82	82	21
292	634.19	635.3	100	78	78	21
293	606.18	607.3	100	83	83	21
294	600.19	601.3	99	37	37	21

[0641]

TABLE 85
295	620.14	621.3	98	74	73	21
296	654.1	655.3	93	69	64	21
297	566.21	567.3	96	71	68	21
298	586.18	587.3	95	72	68	21
299	646.2	647.3	88	92	81	21
300	646.2	647.3	89	81	72	21
301	604.17	605.3	87	93	81	21
302	654.16	655.3	88	88	77	21
303	670.16	671.3	85	100	85	21
304	611.17	612.3	88	100	88	21
306	595.23	596.3	59	100	59	21
308	610.21	611.3	86	100	86	21
309	599.18	600.3	78	98	76	21
310	531.24	532.3	60	81	49	21
311	643.15	644.3	85	89	76	21
312	649.2	650.3	89	100	89	21
313	590.22	591.3	—	—	52	21
314	546.24	547.3	82	100	82	21
315	566.21	567.3	100	82	82	23
316	579.24	580.3	81	92	74	23
317	593.25	594	46	99	45	23
318	608.11	609	100	82	82	23
319	603.24	604.3	63	100	63	23

[0642]

TABLE 86
320	590.13	591.3	74	96	71	23
321	619.13	616.3	77	100	77	21
322	619.13	616.3	87	82	71	21
323	643.23	644.3	100	76	76	21
324	585.17	586	—	—	92	21
325	599.18	600.3	—	—	80	21
326	700.14	701	—	—	84	21
327	634.14	635	75	88	66	21
328	619.13	620.3	100	85	85	21
329	682.16	683.3	97	56	54	21
330	630.24	631.3	70	58	41	21
331	650.21	651.3	98	32	31	21
332	664.22	665.3	8	37	3	21
333	684.17	685.3	10	66	7	21
334	718.13	719	100	43	43	21
335	643.27	644.5	9	49	4	21
336	697.17	698.3	100	57	57	21
337	674.24	675.3	8	25	2	21
338	615.24	616.3	75	51	38	21
339	615.24	616.3	89	45	40	21
340	566.24	567.3	4	68	3	21
341	580.26	581.3	86	53	46	21
342	594.69	595.3	90	37	33	21

[0643]

TABLE 87
343	594.27	595.3	100	41	41	21
344	636.32	637.3	100	62	62	21
345	644.25	645.3	100	18	18	21
346	616.22	617.3	7	28	2	21
347	610.27	611.3	100	48	48	21
348	623.26	624.3	2	94	2	21
349	595.27	596.3	21	55	12	21
350	649.2	650.3	93	57	53	21
352	661.22	662	59	73	43	21
353	707.26	708.3	95	59	56	21
354	649.2	650.3	96	49	47	21
355	663.21	664.3	100	49	49	21
356	764.17	765.3	55	56	31	21
357	698.17	699.3	—	—	16	21
358	683.16	684.3	—	—	17	21
359	679.21	680.3	89	52	46	21
360	614.24	615.3	100	14	14	21
361	634.19	635.3	46	58	27	21
362	668.15	669.3	83	50	42	21
363	630.24	631.3	62	84	52	21
364	622.3	623.3	64	95	61	21
365	630.24	631.3	73	83	61	21
366	601.22	602.3	49	57	28	21

[0644]

TABLE 88
367	601.22	602.3	52	87	45	21
368	566.24	567.3	69	46	32	21
369	580.26	581.3	59	82	48	21
370	580.26	581.3	64	92	59	21
371	678.16	681.3	98	66	65	21
372	668.21	669.3	76	51	39	21
373	684.21	685.3	100	83	83	21
374	656.2	657.3	100	76	76	21
375	616.22	617.3	100	73	73	23
376	629.25	630.3	82	64	52	23
377	643.27	644.3	46	78	36	23
378	658.13	659	100	80	80	23
379	653.25	684.3	97	63	61	23
380	640.14	641.3	100	60	60	23
381	650.21	651.3	90	60	54	21
382	670.15	671.3	76	90	68	21
383	704.12	705.2	67	89	60	21
384	616.22	617.3	82	47	39	21
385	636.19	637.3	85	59	50	21
386	696.21	697.2	79	93	73	21
387	696.21	697.4	96	74	71	21
388	654.18	655.3	97	75	73	21
389	704.18	705.2	82	78	64	21

[0645]

TABLE 89
390	720.18	721.4	90	79	71	21
391	661.19	663.3	93	76	71	21
392	629.25	630.3	93	72	67	21
393	645.25	646.3	76	90	68	21
394	683.16	684.3	69	51	35	21
395	660.22	661.3	40	34	14	21
396	649.2	650.3	56	64	36	21
397	581.25	582.3	64	43	28	21
398	693.17	696.4	30	63	19	21
399	699.22	700.4	63	66	42	21
400	640.23	641.5	18	34	6	21
401	596.25	597.4	75	60	45	21
402	669.14	666.3	100	78	78	21
403	669.14	666.3	96	79	76	21
404	693.25	694.3	100	82	82	21
405	635.18	636.3	100	82	82	21
406	649.2	650.3	100	80	80	21
407	750.15	751.4	93	86	80	21
408	684.15	687	100	80	80	21
409	669.14	670.3	100	100	100	21

[0646]

TABLE 90
		Measured	Hydrolysis
Compound No.	M	value (M + 1)+	yield (%)	Example No.
46	510.18	511.4	73	36
48	526.17	527.2	82	36
49	572.19	573.2	88	36
50	510.18	511.4	82	36
51	572.19	573.2	83	36

Example 38

[0647] Human in vitro IgE Antibody Production Suppressing Activity

[0648] The concentrations of IgE and IgG antibodies were measured by the following method according to the method described in the Journal of Immunology vol.146, pp.1836-1842, 1991 and the Journal of Immunology vol. 147, pp.8-13, 1991.

[0649] Concretely, lymphocyte was separated from the peripheral venous blood of healthy person by density gradient centrifugation. The obtained lymphocyte was washed, suspended in a culture liquid (RPMI-1640 (product of Gibco Co.)+10% heat-inactivated FCS (product of Whittaker Co.)+100 μg/ml streptomycin +100 U/ml penicillin G+2 mM L-glutamine) and cultured for a week in the presence of interleukin 4 (IL-4, product of GENZYME Co.) (0.1 μg/ml), anti-CD40 antibody (antiCD40Aab, product of BIOSOURCE Co.), clone B-B20) (2 μg/ml) and interleukin 10 (IL-10, product of GENZYME Co.) (0.2 μg/ml) in the presence or absence of the compounds of the present invention described in the Tables 10 to 15 at various concentrations as test drugs.

[0650] The culture liquid was added to the culture system, the culture was continued for additional one week, and the concentrations of IgE and IgG antibodies in the supernatant were measured by sandwich ELISA method.

[0651] The measurement by ELISA method was carried out according to the known ELISA method by using rabbit anti-human IgE(ε) antibody (product of ICN Co.) as the primary antibody and biotin-anti-human IgE monoclonal antibody (G7-26, product of PharMingen Co.) as the secondary antibody for the measurement of IgE antibody concentration and anti-human IgG monoclonal antibody (G18-145, product of PharMingen Co.) as the primary antibody and biotin-donkey anti-human IgG antibody (H+L) (product of Jackson Co.) as the secondary antibody for the measurement of IgG antibody concentration, and using avidin-biotin-hourse radish peroxidase (ABC kit, product of Vector Lab.) as the enzyme and TMB (3,3′,5,5′-tetramethylbenzidine) microwell peroxidase substrate system (product of Kirkegaard & Perry Laboratories Inc.) as the substrate.

[0652] The value of IC50 and the suppressing ratio (%) at the test drug concentration of 1 μM were calculated based on the concentration attained in the absence of the compound of the present invention (reference: Ueshima, et al. American Academy of Allergy & Immunology, 1995 Annual ram No.818). Meeting, Program No. 818)

[0653] The results are shown in the Table 91.

TABLE 91
Antibody production suppressing action of the compound
of the present invention (1 μM)
	IgE production	IgG production
Compound	suppressing	suppressing	IC50 (μM)	IC50 (μM)
No.	ratio (%)	ratio (%)	(IgE)	(IgG)
93	56.2	57.9	0.738	>10
		(−91.5)
415	100	−85.8	0.028	9.76
121	100	77.5	0.027	0.543
100	100	100	0.028	0.244
142	100	93.7	0.034	0.141
427	96.4	>10	0.040	>10
351	100	71.7	<0.01	0.662
370	94.7	−45.5	0.027	>1
133	100	98.2	0.042	0.228
79	100	92.4	0.040	0.489
45	99.4	−178.7	0.305	0.631
44	100	88.5	0.221	0.404

[0654] It has been recognized from the results shown in the Table 91 that the compounds of the present invention have IgE antibody production suppressing activity.

[0655] Accordingly, these compounds are expectable as preventives and/or therapeutic agents for allergic diseases, etc., caused by the production of IgE antibody such as bronchial asthma, allergic rhinitis, allergic conjunctivitis, atopic dermatitis, anaphylactic shock, mite allergy, pollinosis, food allergy, urticaria, ulcerative colitis, eosinophilic gastroenteritis and drug-induced rash. Example 39

[0656] Measurement of Cytotoxicity Using Mouse Tumorvcell L929

[0657] [Procedure] The cytotoxic action on tumor cell was measured by neutral red assay (the method described in the Journal of Tissue Culture Methodology, vol.9, p.7 (1984) and ibxicology Letters, vol.24, p.119 (1985)). Concretely, L929 cells (5×104 cells/ml, 10% FCS/RPMI) were added to the wells of a 96 well ELISA plate at a rate of 100 μL each and cultured for a night, and the testing compounds of respective measurement concentrations were dissolved in DMSO solution and added to the above cells. The culture was continued for 3 days, and 2.0 μL of Neutral Red was added to attain the final concentration of 0.01%. The mixture was incubated for 1 hour at 37° C., the supernatant of the cell culture product was removed and the residue was washed twice with 200 μL of PBS to remove excess Neutral Red. Thereafter, the dye taken into the cell was extracted by adding 100 μL of 50% ethanol-1% acetic acid aqueous solution and the amount of the dye was determined by measuring the absorbance at 490 nm. The cytotoxicity was determined at each concentration of the test compound taking the cytotoxicity free from the drug as 100%. The cytotoxicity at each concentration was plotted against the concentration of each test compound and the concentration of the test compound exhibiting 50% cytotoxicity (LD50) was determined. Two sets of measurement were performed for each test under the same condition and the average value was used as the test result. The results are shown in the Table 92.

[0658] Table 92: Cytotoxic Activity of the Compounds of the Present Invention

Compound No. LD50 (μM)
4            0.375
6            2.4
37           1.02
44           1.16
45           0.22
47           0.2
59           2.4
73           >5
74           >5
79           0.98
100          0.95
121          1.8
124          0.14
133          0.33
138          0.13
142          0.54
156          0.30
167          0.18
192          0.26
248          0.085
264          0.156
268          0.16
351          0.31
370          6.8

[0659] It has been recognized from the results shown in the Table 92 that the compounds of the present invention have cytotoxic action on L929.

Example 40

[0660] Carcinostatic Action on Cultured Human Cancer Cell

[0661] [Prodedure] Cultured human cancer cells (39 kinds) were scattered on a 96 well plate, a solution of the testing substance (5-stage concentrations starting from 10−4 M and diluted 10 times to 10.8 M) was added thereto on the next day and the cells were cultured for 2 days. The number of the proliferated cells on each plate was determined by colorimetric quantitative analysis with sulforhodamine B. The concentration to suppress the proliferation of cell by 50% (GI50) compared with a control (free from the testing substance) was calculated and the following values (concentrations) were calculated based on the number of cells immediately before the addition of the testing substance.

[0662] TGI: concentration to suppress the proliferation to a standard cell number (free from the change of apparent number of cells)

[0663] LC50: concentration to decrease the number of cells to 50% of the standard cell number (cytocidal activity)

[0664] The proliferation-suppressing results of three testing substances 124, 257 and 983 on 9 representative cancer cell strains are collectively shown in the Tables 93 to 95.

TABLE 93
Compound	Cancer cell
No.	strain	GI50 (μM)	TGI (μM)	LC50 (μM)
983	HBC-4	0.59	76	>100
	SF-539	0.6	20	51
	HCT-15	0.1	30	>100
	NCI-H460	0.33	16	95
	LOX-IMVI	0.26	3.4	50
	OVCAR-8	4.2	40	>100
	RXF-631L	0.4	18	96
	MKN-74	0.46	25	>100
	PC-3	4.5	31	>100

[0665]

TABLE 94
Compound	Cancer cell
No.	strain	GI50 (μM)	TGI (μM)	LC50 (μM)
124	HBC-4	0.25	18	57
	SF-539	0.13	26	57
	HCT-15	0.17	17	58
	NCI-H460	0.091	14	69
	LOX-IMVI	0.09	10	45
	OVCAR-8	3.1	23	57
	RXF-631L	0.13	12	38
	MKN-74	0.086	16	>100
	PC-3	10	24	55

[0666]

TABLE 95
Compound	Cancer cell
No.	strain	GI50 (μM)	TGI (μM)	LC50 (μM)
257	HBC-4	<0.01	18	58
	SF-539	<0.01	17	51
	HCT-15	<0.01	17	53
	NCI-H460	<0.01	11	44
	LOX-IMVI	<0.01	10	44
	OVCAR-8	<0.01	23	59
	RXF-631L	<0.01	14	42
	MKN-74	<0.01	16	>100
	PC-3	10	26	69

[0667] It has been recognized from the results shown in the Tables 93 to 95 that the compounds of the present invention have proliferation suppressing action on main cultured human cancer cells.

[0668] The results of the Examples 39 and 40 show that the compounds of the present invention are useful also as carcinostatic agents.

[0669] Possibility of Industrial Utilization

[0670] The anthranilic acid derivatives of the present invention or their medically permissible salts or solvates exhibit strong cytotoxic activity and IgE antibody production suppressing action. Accordingly, the anthranilic acid derivatives of the present invention are clinically applicable as a therapeutic agent for cancer or a preventive or therapeutic agent for allergic diseases.

Claims

1. The anthranilic acid derivative expressed by the following formula (1) or the following formula (2) or its pharmacologically permissible salt or solvate;

2. The anthranilic acid derivative described in the claim 1 wherein Y2 is the group of the formula (3)-1 or the formula (3)-2 or its pharmacologically permissible salt or solvate.

3. The anthranilic acid derivative described in the claim 1 and expressed solely by the formula (1), or its pharmacologically permissible salt or solvate.

4. The anthranilic acid derivative described in the claim 1 and expressed solely by the formula (2) wherein the group Y2 is expressed by the formula (3)-1 or the formula (3)-2, or its pharmacologically permissible salt or solvate.

5. The anthranilic acid derivative described in the claim 1 and expressed solely by the formula (2) wherein the group Y2 is expressed by the formula (5)-1 or the formula (5)-2, or its pharmacologically permissible salt or solvate.

6. The anthranilic acid derivative described in the claim 1, 2 or 3 wherein the group Y1 in the formula (1) is expressed by the following formula (9)-1, (9)-2 or (9)-3, or its pharmacologically permissible salt or solvate.

7 The anthranilic acid derivative described in the claim 1, 2, 4 or 5 wherein the group Y2 in the formula (2) is expressed by the formula (5)-1, the formula (5)-2, the formula (9)-1, the formula (9)-2 or the formula (9)-3, or its pharmacologically permissible salt or solvate.

8. The anthranilic acid derivative described in either one of the claims 1 to 7 wherein the group Z in the formula (1) or the formula (2) is a straight-chain, branched or cyclic saturated, unsaturated or aromatic C1 to C12 hydrocarbon group substituted by one or more —NR10R11, —COOR12, —(C═O)NR13R14, —(C═O)R15 or —OR16 [the C1 to C12 hydrocarbon group is optionally further substituted by substituent L (L is a C1 to C6 alkyl group, halogen atom, —NO2 or —CN)], or its pharmacologically permissible salt or solvate.

9. The anthranilic acid derivative described in either one of the claims 1 to 7 wherein the group Z in the formula (1) or the formula (2) is a saturated 3 to 8-membered ring containing one or plural —NR17—, —O— or —S— groups and optionally containing one or more —C(═O)— groups in the ring, or a C1 to C4 straight or branched-chain saturated or unsaturated hydrocarbon group having one or two double bonds or triple bonds and optionally substituted by the above 3 to 8-membered ring, or its pharmacologically permissible salt or solvate.

10. The anthranilic acid derivative described in either one of the claims 1 to 7 wherein the group Z in the formula (1) or the formula (2) is a C5 to C10 straight or branched-chain saturated or unsaturated hydrocarbon group substituted by a monocyclic or bicyclic aromatic ring containing one or more hetero-atoms selected from oxygen, nitrogen and sulfur atom in the ring (the aromatic ring is optionally substituted by a substituent L), or its pharmacologically permissible salt or solvate.

11. A pharmaceutical composition composed of an anthranilic acid derivative described in either one of the claims 1 to 10 or its pharmacologically permissible salt or solvate, and a pharmacologically permissible carrier.

12. A pharmaceutical composition described in the claim 11 and having cytotoxic activity.

13. A therapeutic agent for cancer composed of the pharmaceutical composition described in the claim 11 or 12.

14. A pharmaceutical composition described in the claim 11 and having IgE antibody production suppressing action.

15. A preventive or therapeutic agent for allergic diseases composed of the pharmaceutical composition described in the claim 11 or 14.

16. A preventive or therapeutic agent described in the claim 15 wherein said allergic diseases are bronchial asthma, allergic rhinitis, allergic conjunctivitis, atopic dermatitis, anaphylactic shock, mite allergy, pollinosis, food allergy, urticaria, ulcerative colitis, eosinophilic gastroenteritis or drug-induced rash.