Compounds exhibiting thrombopoietin receptor agonism

TECHNICAL FIELD

The present invention relates to compounds exhibiting thrombopoietin receptor agonism.

BACKGROUND ART

Thrombopoietin, polypeptide cytokine composed of 332 amino acids, activates the production of platelets by stimulating the differentiation and proliferation of megakaryocytes through the receptor and is expected as a medicine for hemopathy accompanied with the unusual number of platelets, for example, thrombocytopenia and the like. DNA sequences encoding the thrombopoietin receptor have been described in Non-Patent 1. Low molecular peptides having an affinity for the thrombopoietin receptor is also known in Patent 1 and Patent 2, but these peptide derivatives are not generally practical for oral administration.

As a low molecule compound having an affinity to the thrombopoietin receptor, 1,4-benzodiazepine derivatives are described in Patent 3 and Patent 4,1-azonaphthalene derivatives are described in Patent 5, N-(4-phenyl-1,3-thiazol-2-yl)carboxamide derivatives are described in Patent 6, Patent 7, Patent 8, Patent 9, and Patent 10.

Patent 1: JP98/72492
Patent 2: WO96/40750
Patent 3: JP99/1477
Patent 4: JP99/152276
Patent 5: WO00/35446
Patent 6: WO01/07423
Patent 7: WO01/53267
Patent 8: WO02/059099
Patent 9: WO02/059100
Patent 10: JP98/287634
Non-Patent 1: Proc. Natl. Acad. Sci., 89, 5640-5644 (1992)

DISCLOSURE OF INVENTION

The object of the present invention is to prepare pharmaceutical compositions exhibiting thrombopoietin receptor agonism and provide orally administrable platelet production modifiers.

In the above situation, the inventors of the present invention have found that the following compounds exhibit strong thrombopoietin receptor agonism.

The present invention relates to:

1) A compound represented by the general formula (I):

wherein R¹is a hydrogen atom, a halogen atom, C1-C6 alkyl, or C1-C12 alkyloxy;

R², R³, and R⁴are each independently a hydrogen atom, a halogen atom, C1-C15 alkyl optionally substituted with one or two substituent(s) selected from substituent group A, C2-C15 alkenyl optionally substituted with one or two substituent(s) selected from substituent group A, C2-C15 alkynyl optionally substituted with one or two substituent(s) selected from substituent group A, C3-C8 cycloalkyl, C1-C15 alkyloxy optionally substituted with one or two substituent(s) selected from substituent group A, or phenyl optionally substituted with one or two substituent(s) selected from substituent group A;

R⁵is a hydrogen atom, a halogen atom, C1-C3 alkyl, C1-C3 alkyloxy, or morpholono;

R⁶is a hydrogen atom, a halogen atom, or C1-C3 alkyl;

R⁷is a halogen atom or C1-C3 alkyl;

R⁸is a halogen atom, C1-C3 alkyl, or C1-C3 alkyloxy;

configuration of double bond substituted with R⁸is E configuration or Z configuration;

R⁹is a hydrogen atom or C1-C6 alkyl; or

R¹and R⁵are taken together with the adjacent carbon atoms may form a 5 to 8 membered ring which may contain a heteroatom(s) and/or an unsaturated bond(s), wherein the ring may be substituted with one or two C1-C8 alkyl;

provided that when R²and R³are a chlorine atom, R⁶is not a hydrogen atom;

substituent group A consists of a halogen atom, C3-C8 cycloalkyl, C3-C8 cycloalkenyl, phenyl, naphthyl, pyridyl, oxolanyl, cyano, C1-C12 alkyloxy, C2-C12 alkenyloxy, C2-C12 alkynyloxy, C3-C8 cycloalkyl-C1-C8 alkyloxy, phenyl-C1-C8 alkyloxy, naphthyl-C1-C8 alkyloxy, C1-C8 alkyloxy-C1-C8 alkyloxy, (C1-C8 alkyloxy-C1-C8 alkyloxy)C1-C8 alkyloxy, di(C1-C8 alkyloxy)C1-C8 alkyloxy, oxolanyl-C1-C8 alkyloxy, haloC1-C8 alkyloxy, C3-C8 cycloalkyloxy, amino optionally substituted with C1-C8 alkyl, C1-C8 alkylthio, and C1-C8 alkylthio-C1-C8 alkyloxy;

a pharmaceutically acceptable salt, or solvate thereof,

2) A compound of 1), wherein both of R⁶and R⁷are a fluorine atom or a chlorine atom, a pharmaceutically acceptable salt, or solvate thereof,

3) A compound of 1) or 2), wherein R⁵is a hydrogen atom or C1-C3 alkyloxy, a pharmaceutically acceptable salt, or solvate thereof,

4) A compound of any one of 1) to 3), wherein R⁸is methyl or methyloxy, a pharmaceutically acceptable salt, or solvate thereof,

5) A compound of any one of 1) to 4), wherein R²is C1-C15 alkyl optionally substituted with one or two substituent(s) selected from substituent group A, C2-C15 alkynyl optionally substituted with one or two substituent(s) selected from substituent group A, or C1-C15 alkyloxy optionally substituted with one or two substituent(s) selected from substituent group A, a pharmaceutically acceptable salt, or solvate thereof,

6) A compound of any one of 1) to 4), wherein R²is C1-C12 alkyl optionally substituted with one or two C1-C8 alkyloxy, and both of R³and R⁴are a hydrogen atom, a pharmaceutically acceptable salt, or solvate thereof,

7) A compound represented by the general formula (II):

wherein R^Ais a hydrogen atom, C1-C12 alkyloxy, C1-C8 alkyloxy-C1-C8 alkyloxy or (C1-C8 alkyloxy-C1-C8 alkyloxy)C1-C8 alkyloxy;

R^Bis C1-C14 alkyl optionally substituted with one or two substituent(s) selected from substituent group B, C2-C14 alkynyl optionally substituted with one or two substituent(s) selected from substituent group B, C3-C8 cycloalkyl, C1-C14 alkyloxy optionally substituted with one or two substituent(s) selected from substituent group B, phenyl, or naphthyl;

R^Cis a hydrogen atom, a halogen atom, C1-C6 alkyl, or C1-C12 alkyloxy;

R^Dis a hydrogen atom, a halogen atom, C1-C3 alkyl, C1-C3 alkyloxy, or morpholino;

R⁶and R⁷are each independently a halogen atom or C1-C3 alkyl;

R⁸is a halogen atom, C1-C3 alkyl, or C1-C3 alkyloxy;

configuration of double bond substituted with R⁸is E configuration or Z configuration;

substituent group B consists of a halogen atom, C3-C8 cycloalkyl, C3-C8 cycloalkenyl, phenyl, naphthyl, pyridyl, oxolanyl, cyano, C1-C8 alkyloxy, C2-C8 alkenyloxy, C2-C8 alkynyloxy, C3-C8 cycloalkyl-C1-C8 alkyloxy, phenyl-C1-C8 alkyloxy, naphthyl-C1-C8 alkyloxy, C1-C8 alkyloxy-C1-C8 alkyloxy, (C1-C8 alkyloxy-C1-C8 alkyloxy)C1-C8 alkyloxy, di(C1-C8 alkyloxy)C1-C8 alkyloxy, oxolanyl-C1-C8 alkyloxy, haloC1-C8 alkyloxy, C3-C8 cycloalkyloxy, amino optionally substituted with C1-C8 alkyl, C1-C8 alkylthio, and C1-C8 alkylthio-C1-C8 alkyloxy;

a pharmaceutically acceptable salt, or solvate thereof,

8) A compound of 7), wherein both of R⁶and R⁷are a fluorine atom or a chlorine atom, a pharmaceutically acceptable salt, or solvate thereof,

9) A compound of 7) or 8), wherein R⁸is methyl or methyloxy, a pharmaceutically acceptable salt, or solvate thereof,

10) A compound of any one of 7) to 9), wherein R^Cis a fluorine atom or C1-C3 alkyloxy, a pharmaceutically acceptable salt, or solvate thereof,

11) A compound of any one of 7) to 10), wherein R^Ais C1-C8 alkyloxy; R^Bis C1-C11 alkyl optionally substituted with one or two substituent(s) selected from substituent group B, C2-C11 alkynyl optionally substituted with one or two substituent(s) selected from substituent group B, a pharmaceutically acceptable salt, or solvate thereof,

12) A compound of 7), wherein R^Cis a fluorine atom or C1-C3 alkyloxy, R^Dis a hydrogen atom or C1-C3 alkyloxy, both of R⁶and R⁷are a fluorine atom or a chlorine atom, R⁸is methyl or methyloxy, R^Ais C1-C3 alkyloxy, R^Bis C8-C12 alkyl optionally substituted with one or two substituent(s) selected from substituent group B, a pharmaceutically acceptable salt, or solvate thereof,

13) A compound represented by the general formula (III):

wherein R^Eis C1-C15 alkyl optionally substituted with one or two substituent(s) selected from substituent group C, C2-C15 alkynyl optionally substituted with one or two substituent(s) selected from substituent group C, or C1-C15 alkyloxy optionally substituted with one or two substituent(s) selected from substituent group C;

Z is straight-chain C1-C4 alkylene optionally substituted with C1-C8 alkyl, which may contain an optionally substituted a heteroatom(s) or straight-chain C2-C4 alkenylene optionally substituted with C1-C8 alkyl, which may contain an optionally substituted heteroatom(s);

R⁶and R⁷are each independently a halogen atom or C1-C3 alkyl;

R⁸is a halogen atom, C1-C3 alkyl, or C1-C3 alkyloxy;

configuration of double bond substituted with R⁸is E configuration or Z configuration;

substituent group C consists of a halogen atom, C3-C8 cycloalkyl, C3-C8 cycloalkenyl, phenyl, naphthyl, pyridyl, oxolanyl, cyano, C1-C8 alkyloxy, C2-C8 alkenyloxy, C2-C8 alkynyloxy, C3-C8 cycloalkyl-C1-C8 alkyloxy, phenyl-C1-C8 alkyloxy, naphthyl-C1-C8 alkyloxy, C1-C8 alkyloxy-C1-C8 alkyloxy, (C1-C8 alkyloxy-C1-C8 alkyloxy)C1-C8 alkyloxy, di(C1-C8 alkyloxy)C1-C8 alkyloxy, oxolanyl-C1-C8 alkyloxy, haloC1-C8 alkyloxy, C3-C8 cycloalkyloxy, amino optionally substituted with C1-C8 alkyl, C1-C8 alkylthio, and C1-C8 alkylthio-C1-C8 alkyloxy;

a pharmaceutically acceptable salt, or solvate thereof,

14) A compound of 13), wherein both of R⁶and R⁷are a fluorine atom or a chlorine atom, a pharmaceutically acceptable salt, or solvate thereof,

15) A compound of 13) or 14), wherein R⁸is methyl or methyloxy, a pharmaceutically acceptable salt, or solvate thereof,

16) A compound of any one of 13) to 15), wherein Z is C1-C14 alkylene, —O—(C1-C3 alkylene)-, or —(C1-C3 alkylene)-O—, a pharmaceutically acceptable salt, or solvate thereof,

17) A compound of any one of 13) to 16), wherein R^Eis C1-C10 alkyl optionally substituted with one or two substituent(s) selected from substituent group C, C2-C10 alkynyl optionally substituted with one or two substituent(s) selected from substituent group C, or C1-C10 alkyloxy optionally substituted with one or two substituent(s) selected from substituent group C, a pharmaceutically acceptable salt, or solvate thereof,

18) A compound of 13), wherein both of R⁶and R⁷are a fluorine atom or a chlorine atom, R⁸is methyl or methyloxy, R^Eis C1-C8 alkyl optionally substituted with one or two C1-C6 alkyloxy, Z is C1-C2 alkylene, a pharmaceutically acceptable salt, or solvate thereof,

19) A compound represented by the general formula (II-A):

wherein R^Cis a hydrogen atom, a halogen atom, C1-C6 alkyl, or C1-C12 alkyloxy;

R^Dis a hydrogen atom, a halogen atom, C1-C3 alkyl, C1-C3 alkyloxy, or morpholino;

R^Fis C1-C14 alkyl optionally substituted with one or two substituent(s) selected from substituent group D, C2-C14 alkenyl optionally substituted with one or two substituent(s) selected from substituent group D, C2-C14 alkynyl optionally substituted with one or two substituent(s) selected from substituent group D, C1-C14 alkyloxy optionally substituted with one or two substituent(s) selected from substituent group C, C3-C8 cycloalkyl, or phenyl optionally substituted with one or two substituent(s) selected from substituent group D;

R⁶and R⁷are each independently a halogen atom or C1-C3 alkyl;

R⁸is a halogen atom, C1-C3 alkyl, or C1-C3 alkyloxy;

substituent group D consists of a halogen atom, C3-C8 cycloalkyl, C3-C8 cycloalkenyl, phenyl, naphthyl, pyridyl, oxolanyl, cyano, C1-C8 alkyloxy, C2-C8 alkenyloxy, C2-C8 alkynyloxy, C3-C8 cycloalkyl-C1-C8 alkyloxy, phenyl-C1-C8 alkyloxy, naphthyl-C1-C8 alkyloxy, C1-C8 alkyloxy-C1-C8 alkyloxy, (C1-C8 alkyloxy-C1-C8 alkyloxy)C1-C8 alkyloxy, di(C1-C8 alkyloxy)C1-C8 alkyloxy, oxolanyl-C1-C8 alkyloxy, haloC1-C8 alkyloxy, C3-C8 cycloalkyloxy, amino optionally substituted with C1-C8 alkyl, C1-C8 alkylthio, and C1-C8 alkylthio-C1-C8 alkyloxy;

a pharmaceutically acceptable salt, or solvate thereof,

20) A compound of 19), wherein both of R⁶and R⁷are a fluorine atom or a chlorine atom, a pharmaceutically acceptable salt, or solvate thereof,

21) A compound of claim 19), wherein R⁸is methyl or methyloxy, a pharmaceutically acceptable salt, or solvate thereof,

22) A compound of 19), wherein R^Cis a fluorine atom or C1-C3 alkyloxy, a pharmaceutically acceptable salt, or solvate thereof,

23) A compound of any one of 19) to 22), wherein R^Eis C1-C14 alkyl optionally substituted with one or two substituent(s) selected from substituent group D, C2-C14 alkynyl optionally substituted with one or two substituent(s) selected from substituent group D, or C1-C14 alkyloxy optionally substituted with one or two substituent(s) selected from substituent group D, a pharmaceutically acceptable salt, or solvate thereof,

24) A pharmaceutical composition containing a compound as an active ingredient, a pharmaceutically acceptable salt, or solvate thereof of any one of 1) to 23),

25) A pharmaceutical composition containing a compound as an active ingredient, a pharmaceutically acceptable salt, or solvate thereof of any one of 1) to 23), which is exhibiting thrombopoietin receptor agonism,

26) A platelet production modifier which contains a compound as an active ingredient, a pharmaceutically acceptable salt, or solvate thereof of any one of 1) to 23),

27) Use of a compound, a pharmaceutically acceptable salt, or solvate thereof of any one of 1) to 23) for preparation of a pharmaceutical composition for modifiering a platelet production,

28) A method for modifiering a platelet production of a mammal, including a human, which comprises administration to said mammal of a compound, a pharmaceutically acceptable salt, or solvate thereof of any one of 1) to 23) in a pharmaceutically effective amount.

In the present specification, the term “halogen atom” means fluorine atom (fluoro), chlorine atom (chloro), bromine atom (bromo), and iodine atom (iodo).

In the present specification, nitrogen atom, oxygen atom, sulfur atom, and the like are exemplified as “heteroatom”.

In the present specification, the term “alkyl” employed alone or in combination with other term includes a straight- or branched chain alkyl having contains forward-mentioned number of carbon. Methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, n-pentyl, isopentyl, neo-pentyl, n-hexyl, isohexyl, n-heptyl, n-octyl, n-nonyl, n-decyl, n-undecyl, n-dodecyl, n-tridecyl, n-tetradecyl, n-pentadecyl, and the like are exemplified as “alkyl”.

In the present specification, the term “alkenyl” employed alone or in combination with other term includes a straight- or branched chain alkenyl having forward-mentioned number of carbon. Ethenyl, 2-propen-1-yl, 3-butene-1-yl, 14-pentadecen-1-yl, and tke like are exemplified as “alkenyl”.

In the present specification, the term “alkynyl” employed alone or in combination with other term includes a straight- or branched chain alkynyl having forward-mentioned number of carbon. Ethynyl, 1-propyn-1-yl, 1-butyn-1-yl, 1-pentyn-1-yl, 1-hexyn-1-yl, 1-heptyn-1-yl, 1-decyn-1-yl, 1-pentadecyn-1-yl, and the like are exemplified as “alkynyl”.

In the present specification, the term “cycloalkyl” employed alone or in combination with other term includes a mono-carbocyclic group having forward-mentioned number of carbon. Cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, and the like are exemplified as “cycloalkyl”.

In the present specification, the term “cycloalkenyl” employed alone or in combination with other term includes a mono-carbocyclic group having forward-mentioned number of carbon and one or more double bond(s). Cyclopropenyl, 1-cyclobuten-1-yl, 1-cyclopenten-1-yl, 1-cyclohexen-1-yl, 1-cyclohepten-1-yl, 1-cycloocten-1-yl, and the like are exemplified as “cycloalkenyl”.

In the present specification, the term “naphthyl” means 1-naphthyl or 2-naphthyl.

In the present specification, the term “pyridyl” means 2-pyridyl, 3-pyridyl or 4-pyridyl.

In the present specification, the term “oxolanyl” means 2-oxolanyl or 3-oxolanyl.

In the present specification, the term “alkyloxy” employed alone or in combination with other term includes alkyloxy having forward-mentioned number of carbon. Methyloxy, ethyloxy, n-propyloxy, isopropyloxy, n-butyloxy, isobutyloxy, sec-butyloxy, tert-butyloxy, n-pentyloxy, isopentyloxy, neo-pentyloxy, n-hexyloxy, isohexyloxy, n-heptyloxy, n-octyloxy, n-nonyloxy, n-decyloxy, n-undecyloxy, n-dodecyloxy, n-pentadecyloxy, and the like are exemplified as “alkyloxy”.

In the present specification, the term “haloalkyloxy” employed alone or in combination with other term includes the above-mentioned “alkyloxy” substituted with one or more halogen atom(s). Chloromethyloxy, difluoromethyloxy, 2,2,2-trifluoroethyloxy, 3-chloropropyloxy, 4-fluorobutyloxy, and the like are exemplified as “haloalkyloxy”.

In the present specification, the term “alkenyloxy” employed alone or in combination with other term includes the above-mentioned “alkenyl” substituted with one or more hydroxy. 2-Propenyloxy, 3-butenyloxy, 4-octenyloxy, and the like are exemplified as “alkenyloxy”.

In the present specification, the term “alkynyloxy” employed alone or in combination with other term includes the above-mentioned “alkynyl” substituted with one or more hydroxy. 2-Propynnyloxy, 3-butynyloxy, 4-octynyloxy, and the like are exemplified as “alkynyloxy”.

In the present specification, cylopropylmethyloxy, 2-cylopropylethyloxy, 2-cylobutylethyloxy, 3-cylopentylpropyloxy, cylohexylmethyloxy, 4-cylohexylbutyloxy, 8-cylooctyloctyloxy, and the like are exemplified as “C3-C8 cycloalkyl-C1-C8 alkyloxy”.

In the present specification, phenylmethyloxy, 2-phenylethyloxy, 3-phenylpropyloxy, 4-phenylbutyloxy, 8-phenyloctyloxy, and the like are exemplified as “phenyl-C1-C8 alkyloxy”.

In the present specification, 1-naphthylmethyloxy, 2-naphthylmethyloxy, 2-(1-naphthyl)ethyloxy, 3-(2-naphthyl)propyloxy, 4-(1-naphthyl)butyloxy, 8-(2-naphthyl)octyloxy, and the like are exemplified as “naphthyl-C1-C8 alkyloxy”.

In the present specification, 2-methyloxyethyloxy, 2-ethyloxyethyloxy, 3-methyloxypropyloxy, 4-ethyloxybutyloxy, and the like are exemplified as “C1-C4 alkyloxy-C2-C4 alkyloxy”.

In the present specification, methyloxymethyloxy, 2-methyloxyethyloxy, 2-ethyloxyethyloxy, 3-methyloxypropyloxy, 4-ethyloxybutyloxy, 6-butyloxyhexyloxy, 8-octyloxyoctyloxy, and the like are exemplified as “C1-C8 alkyloxy-C1-C8 alkyloxy”.

In the present specification, 2-(methyloxymethyloxy)ethyloxy, 2-(2-ethyloxyethyloxy)ethyloxy, 3-(2-methyloxyethyloxy)propyloxy, 4-(2-ethyloxyethyloxy)butyloxy, and the like are exemplified as “(C1-C4 alkyloxy-C2-C4 alkyloxy)C2-C4 alkyloxy”.

In the present specification, 2-(2-methyloxyethyloxy)ethyloxy, 2-(2-ethyloxyethyloxy)ethyloxy, 3-(2-methyloxyethyloxy)propyloxy, 4-(2-ethyloxyethyloxy)butyloxy, 8-(2-butyloxyethyloxy)octyloxy, and the like are exemplified as “(C1-C8alkyloxy-C1-C8 alkyloxy)C1-C8 alkyloxy”.

In the present specification, 1,3-di(methyloxy)-2-propyloxy, 1,3-di(ethyloxy)-2-propyloxy, 1-ethyloxy-3-methyloxy-2-propyloxy, and the like are exemplified as “di(C1-C8alkyloxy)C1-C8 alkyloxy”.

In the present specification, “oxolanyl-C1-C8 alkyloxy” means the above-mentioned “C1-C8 alkyloxy” substituted with oxolanyl. Examples of oxolanyl-C1-C8 alkyloxy includes 2-oxolanyletyloxy, 3-oxolanylpropyloxy, 4-oxolanylbutyloxy, 8-oxolanyloctyloxy, and the like.

In the present specification, the term “cycloalkyloxy” employed alone or in combination with other term includes an oxygen atom substituted with a mono-carbocyclic group having forward-mentioned number of carbon. Cycloalkyloxy include cyclopropyloxy, cyclobutyloxy, cyclopentyloxy, cyclohexyloxy, cyclooctynyloxy, and the like are exemplified as “cycloalkyloxy”.

In the present specification, the term “alkylthio” employed alone or in combination with other term includes a straight- or branched chain alkylthio having forward-mentioned number of carbon. Alkylthio include methylthio, ethylthio, n-propylthio, isopropylthio, n-butylthio, isobutylthio, sec-butylthio, tert-butylthio, n-pentylthio, isopentylthio, neo-pentylthio, n-hexylthio, isohexylthio, n-heptylthio, n-octylthio, and the like are exemplified as “alkylthio”.

In the present specification, 2-methylthioethyloxy, 2-ethylthioethyloxy, 3-methylthiopropyloxy, 4-ethylthiobutyloxy, 8-butylthiooctyloxy, and the like are exemplified as “C1-C8 alkylthio-C1-C8 alkyloxy”.

In the present specification, the term “C1-C2 alkylene” means methylene and ethylene.

In the present specification, the term “straight-chain C1-C4 alkylene” means straight-chain alkylene having one to four carbon atom(s). Methylene, ethylene, trimethylene, and teteramethylene are exemplified as “straight-chain C1-C4 alkylene”.

In the present specification, the term “C1-C3 alkylene” means straight-chain alkylene having one to three carbon atom(s). Methylene, ethylene, and trimethylene are exemplified as “C1-C3 alkylene”.

In the present specification, the term “straight-chain C1-C4 alkylene optionally substituted with C1-C8 alkyl, which may contain optionally substituted a heteroatom(s)” means straight-chain alkylene having one to four carbon atom(s) which may contain optionally substituted one to three heteroatom(s) optionally substituted with C1-C8 alkyl and the alkylene may be optionally substituted with C1-C8 alkyl. Examples are —CH₂—, —CH₂CH₂—, —CH(n-C₄H₉)CH₂—, —CH(n-C₆H₁₃)CH₂—, —CH(n-C₇H₁₅)CH₂—, —CH₂CH₂CH₂—, —CH₂CH₂CH₂CH₂—, —CH₂O—, —OCH₂—, —SCH₂—, —OCH₂O—, —OCH₂CH₂O—, —CH₂CH₂OCH₂CH₂—, and the like.

In the present specification, the term “straight-chain C2-C4 alkenylene optionally substituted with C1-C8 alkyl, which may contain optionally substituted a heteroatom(s)” means straight-chain alkenylene having two to four carbon atom(s) which may contain optionally substituted one to three heteroatom(s) optionally substituted with C1-C8 alkyl and the alkenylne may be optionally substituted with C1-C8 alkyl. Examples are —CH═CH—, —O—CH═CH—, —S—CH═CH—, —O—CH═CH—O—, and the like.

In the present specification, C1-C8 alkyl is exemplified as “optionally substituted heteroatom”.

In the present specification, cyclopentadiene, benzene, cyclohexadiene, cycloheptadiene, furan, thiophen, pyran, and the like are exemplified as “5 to 8 membered ring taken together with the adjacent carbon atoms which may contain a heteroatom(s) and/or an unsaturated bond(s)”.

In the present specification, the term “amino optionally substituted with C1-C8 alkyl” means non-substituted amino and amino substituted with one or two C1-C8 alkyl. Examples are amino, monomethylamino, dimethylamino, ethylamino, diethylamino, and the like.

Preferable are a fluorine atom and a chlorine atom as “halogen atom” for R¹, R², R³, R⁴, R⁵, R^C, and R^D. Especially, a fluorine atom is preferable.

Preferable are a fluorine atom and a chlorine atom as “halogen atom” for R⁶, R⁷, and R⁸.

Preferable are C1-C4 alkyl as “C1-C6 alkyl” for R¹, R⁹, and R^C. Especially, methyl or ethyl is preferable.

Preferable is methyl as “C1-C3 alkyl” for R⁵, R⁶, R⁷, R⁸, and R^D.

Preferable are C1-C8 alkyloxy as “C1-C12 alkyloxy” for R¹and R^C. Especially, methyloxy or ethyloxy is preferable.

Preferable is methyloxy as “C1-C3 alkyloxy” for R⁵, R⁸, and R^D.

Preferable is C1-C12 alkyl as “C1-C15 alkyl” of “C1-C15 alkyl optionally substituted with substituent(s) selected from substituent group A” for R², R³, and R⁴. Preferable are C5-C6 cycloalkyl, C1-C8 alkyloxy, C1-C4 alkyloxy-C2-C4alkyloxy, (C1-C4 alkyloxy-C2-C4alkyloxy)C2-C4 alkyloxy, or methylthio as “substituent(s) selected from substituent group A”. Preferable is one or two as “number(s) of substituent(s)”.

Preferable is a 5 to 6 membered ring which may contain a heteroatom(s) and/or an unsaturated bond(s) as “R¹and R⁵taken together with the adjacent carbon atoms may form a 5 to 8 membered ring which may contain a heteroatom(s) and/or an unsaturated bond(s)”. Preferable are an oxygen atom, a sulfur atom, or a nitrogen atom as heteroatom. Preferable is one as a number of heteroatom. Preferable is a double bond as an unsaturated bond. Preferable is one as a number of double bond.

Preferable is C1-C8 alkyloxy as “C1-C12 alkyloxy” for R^A.

Preferable is C1-C4 alkyloxy-C2-C4 alkyloxy as “C1-C8 alkyloxy-C1-C8alkyloxy” for R^A.

Preferable is (C1-C4 alkyloxy-C2-C4 alkyloxy)C2-C4 alkyloxy as “(C1-C8 alkyloxy-C1-C8alkyloxy)C1-C8 alkyloxy” for R^A.

Preferable is C1-C12 alkyl as “C1-C14 alkyl” of “straght- or branched chain C1-C14 alkyl optionally substituted with substituent(s) selected from substituent group B” for R^B. Preferable are C5-C6 cycloalkyl, C1-C8 alkyloxy, C1-C4 alkyloxy-C2-C4alkyloxy, (C1-C4 alkyloxy-C2-C4alkyloxy)C2-C4 alkyloxy, or methylthio as “substituent(s) selected from substituent group B”. Preferable is one as “number of substituent(s)”.

Preferable is C1-C10 alkyl as “C1-C15 alkyl” of “straght- or branched chain C1-C15 alkyl optionally substituted with substituent(s) selected from substituent group C” for R^E. Especially, C1-C8 alkyl is preferable. Preferable are C5-C6 cycloalkyl, C1-C8 alkyloxy, C1-C4 alkyloxy-C2-C4alkyloxy, (C1-C4 alkyloxy-C2-C4alkyloxy)C2-C4 alkyloxy, or methylthio as “substituent(s) selected from substituent group C”. Especially, C1-C6 alkyloxy is preferable. Preferable is one or two as “number of substituent(s)”.

Preferable are C1-C4 alkylene, —O—(C1-C3 alkylene), (C1-C3 alkylene)-O— as “straght-chain C1-C4 alkylene optionally substituted with C1-C8 alkyl, which may contain optionally substituted heteroatom” for Z. Especially, C1-C2 alkylene or —OCH₂O— is preferable.

Substituents groups (Ia) to (Io) are shown as preferable substituent(s) groups for R¹to R⁹of the compound represented by general formula (I)

For R¹, (Ia) a hydrogen atom, a halogen atom, or C1-C6 alkyloxy, (Ib) halogen atom or C1-C6 alkyloxy.

For R², (Ic) C1-C15 alkyl substituted with one or same or different two substituent(s) selected from substituent group consists of (C5-C6 cycloalkyl, C1-C8 alkyloxy, C1-C4 alkyloxy-C2-C4 alkyloxy, (C1-C4 alkyloxy-C2-C4 alkyloxy)C2-C4 alkyloxy, and methylthio), C2-C15 alkynyl substituted with one or same or different two substituent(s) selected from substituent group consists of (C5-C6 cycloalkyl, C1-C8 alkyloxy, C1-C4 alkyloxy-C2-C4 alkyloxy, (C1-C4 alkyloxy-C2-C4 alkyloxy)C2-C4 alkyloxy, and methylthio) or C1-C15 alkyloxy substituted with one or same or different two substituent(s) selected from substituent group consists of (C5-C6 cycloalkyl, C1-C8 alkyloxy, C1-C4 alkyloxy-C2-C4 alkyloxy, (C1-C4 alkyloxy-C2-C4 alkyloxy)C2-C4 alkyloxy, and methylthio), (Id) C1-C15 alkyl substituted with one substituent selected from substituent group consists of (C1-C8 alkyloxy and C1-C4 alkyloxy-C2-C4 alkyloxy), C2-C15 alkynyl substituted with one substituent selected from substituent group consists of (C1-C8 alkyloxy and C1-C4 alkyloxy-C2-C4 alkyloxy), or C1-C15 alkyloxy substituted with one substituent selected from substituent group consists of (C1-C8 alkyloxy and C1-C4 alkyloxy-C2-C4 alkyloxy), (Ie) C1-C15 alkyl substituted with one C1-C8 alkyloxy, C2-C15 alkynyl substituted with one C1-C8 alkyloxy, or C1-C15 alkyloxy substituted with one C1-C8 alkyloxy.

For R³, R⁴, and R⁵, (If) each independently a hydrogen atom or C1-C3 alkyloxy.

For R^Gand R⁷, (Ig) each independently a halogen atom.

For R⁸, (Ih) a halogen atom, C1-C3 alkyl, or C1-C3 alkyloxy, (Ii) C1-C3 alkyl or C1-C3 alkyloxy, (Ij) C1-C3 alkyl.

For R⁹, (Ik) a hydrogen atom.

Or, R¹and R⁵may form a (Il) 5 to 6 membered ring taken together with the adjacent carbon atoms which may contain an oxygen atom, (Im) 6 membered carbocylic ring taken together with the adjacent carbon atoms, (In) 6 membered ring taken together with the adjacent carbon atoms which contains one oxygen atom.

Examples of preferable group of the compound represented by general formula (I) contains [R¹, R², R³, R⁴, R⁵, R⁶, R⁷, R⁸, R⁹]=[Ia, Ic, If, If, If, Ig, Ig, Ih, Ik], [Ia, Ic, If, If, If, Ig, Ig, Ii, Ik], [Ia, Ic, If, If, If, Ig, Ig, Ij, Ik], [Ia, Id, If, If, If, Ig, Ig, Ih, Ik], [Ia, Id, If, If, If, Ig, Ig, Ii, Ik], [Ia, Id, If, If, If, Ig, Ig, Ij, Ik], [Ia, Ie, If, If, If, Ig, Ig, Ih, Ik], [Ia, Ie, If, If, If, Ig, Ig, Ii, Ik], [Ia, Ie, If, If, If, Ig, Ig, Ij, Ik], [Ib, Ic, If, If, If, Ig, Ig, Ih, Ik], [Ib, Ic, If, If, If, Ig, Ig, Ii, Ik], [Ib, Ic, If, If, If, Ig, Ig, Ij, Ik], [Ib, Id, If, If, If, Ig, Ig, Ih, Ik], [Ib, Id, If, If, If, Ig, Ig, Ii, Ik], [Ib, Id, If, If, If, Ig, Ig, Ij, Ik], [Ib, Ie, If, If, If, Ig, Ig, Ih, Ik], [Ib, Ie, If, If, If, Ig, Ig, Ii, Ik], [Ib, Ie, If, If, If, Ig, Ig, Ij, Ik], or [R¹—R⁵, R², R³, R⁴, R⁶, R⁷, R⁸, R⁹]=[Il, Ic, If, If, Ig, Ig, Ih, Ik], [Il, Ic, If, If, Ig, Ig, Ii, Ik], [Il, Ic, If, If, Ig, Ig, Ij, Ik], [Il, Id, If, If, Ig, Ig, Ih, Ik], [Il, Id, If, If, Ig, Ig, Ii, Ik], [Il, Id, If, If, Ig, Ig, Ij, Ik], [Il, Ie, If, If, Ig, Ig, Ih, Ik], [Il, Ie, If, If, Ig, Ig, Ii, Ik], [Il, Ie, If, If, Ig, Ig, Ij, Ik], [Im, Ic, It If, Ig, Ig, Ih, Ik], [Im, Ic, If, If, Ig, Ig, Ii, Ik], [Im, Ic, If If, Ig, Ig, Ij, Ik], [Im, Id, If, If, Ig, Ig, Ih, Ik], [Im, Id, If, If, Ig, Ig, Ii, Ik], [Im, Id, If, If, Ig, Ig, Ij, Ik], [Im, Ie, If, If, Ig, Ig, Ih, Ik], [Im, Ie, If, If, Ig, Ig, Ii, Ik], [Im, Ie, If, If, Ig, Ig, Ij, Ik], [In, Ic, If If, Ig, Ig, Ih, Ik], [In, Ic, If If, Ig, Ig, Ii, Ik], [In, Ic, If, If, Ig, Ig, Ij, Ik], [In, Id, If, If, Ig, Ig, Ih, Ik], [In, Id, If, If, Ig, Ig, Ii, Ik], [In, Id, If, If, Ig, Ig, Ij, Ik], [In, Ie, If, If, Ig, Ig, Ih, Ik], [In, Ie, If, If, Ig, Ig, Ii, Ik], [In, Ie, If, If, Ig, Ig, Ij, Ik].

Substituents groups (IIa) to (IIn) are shown as preferable substituent(s) groups for R⁶to R⁸and R^Ato R^Dof the compound represented by general formula (II)

For R⁶and R⁷, (IIa) each independently a halogen atom.

For R⁸, (IIb) a halogen atom, C1-C3 alkyl, or C1-C3 alkyloxy, (IIc) C1-C3 alkyl or C1-C3 alkyloxy, (IId) C1-C3 alkyl.

For R^A, (IIe) a hydrogen atom, C1-C8 alkyloxy, or C1-C4 alkyloxy-C2-C4 alkyloxy, (IIf) C1-C8 alkyloxy, (IIg) C1-C4 alkyloxy-C2-C4 alkyloxy.

For R^B, (IIh) C1-C14 alkyl substituted with one substituent selected from substituent group consists of (a hydrogen atom, C1-C8 alkyloxy, and C1-C4 alkyloxy-C2-C4 alkyloxy), C2-C14 alkynyl substituted with one substituent selected from substituent group consists of (a hydrogen atom, C1-C8 alkyloxy, and C1-C4 alkyloxy-C2-C4 alkyloxy), or C1-C14 alkyloxy substituted with one substituent selected from substituent group consists of (a hydrogen atom, C1-C8 alkyloxy, and C1-C4 alkyloxy-C2-C4 alkyloxy), (IIi) C1-C14 alkyl, (IIj) C1-C14 alkyl substituted with one C1-C8 alkyloxy, C2-C14 alkynyl substituted with one C1-C8 alkyloxy, or C1-C14 alkyloxy substituted with one C1-C8 alkyloxy, (IIk) C1-C14 alkyl substituted with one C1-C4 alkyloxy-C2-C4 alkyloxy, C2-C14 alkynyl substituted with one C1-C4 alkyloxy-C2-C4 alkyloxy, or C1-C14 alkyloxy substituted with one C1-C4 alkyloxy-C2-C4 alkyloxy.

For R^C, (IIl) a hydrogen atom, a halogen atom, or C1-C6 alkyloxy, (IIm) halogen atom or C1-C6 alkyloxy.

For R^D, (IIn) a hydrogen atom or C1-C3 alkyloxy.

Examples of preferable group of the compound represented by general formula (II) contains [R⁶, R⁷, R⁸, R^A, R^B, R^C, R^D]=[IIa, IIa, IIb, IIe, IIh, III, IIn], [IIa, IIa, IIb, IIe, IIh, IIm, IIn], [IIa, IIa, IIb, IIe, IIi, IIl, IIn], [IIa, IIa, IIb, IIe, IIi, IIm, IIn], [IIa, IIa, IIb, IIe, IIj, IIl, IIn], [IIa, IIa, IIb, IIe, IIj, IIm, IIn], [IIa, IIa, IIb, IIe, IIk, IIl, IIn], [IIa, IIa, IIb, IIe, IIk, IIm, IIn], [IIa, IIa, IIb, IIf, IIh, IIl, IIn], [IIa, IIa, IIb, IIf, IIh, IIm, IIn], [IIa, IIa, IIb, IIf, IIi, IIl, IIn], [IIa, IIa, IIb, IIf, IIi, IIm, IIn], [IIa, IIa, IIb, IIf, IIj, IIl, IIn], [IIa, IIa, IIb, IIf, IIj, IIm, IIn], [IIa, IIa, IIb, IIf, IIk, IIl, IIn], [IIa, IIa, IIb, IIf, IIk, IIm, IIn], [IIa, Ia, IIb, IIg, IIh, IIl, IIn], [IIa, IIa, IIb, IIg, IIh, IIm, IIn], [IIa, IIa, IIb, IIg, IIi, IIl, IIn], [IIa, IIa, IIb, IIg, IIi, IIm, IIn], [IIa, IIa, IIb, IIg, IIj, IIl, IIn], [IIa, IIa, IIb, IIg, IIj, IIm, IIn], [IIa, IIa, IIb, IIg, IIk, IIl, IIn], [IIa, IIa, IIb, IIg, IIk, IIm, IIn], [IIa, Iha, IIc, IIe, IIh, IIl, IIn], [IIa, IIa, IIc, IIe, IIh, IIm, IIn], [IIa, IIa, IIc, IIe, IIi, IIl, IIn], [IIa, IIa, IIc, IIe, IIi, IIm, IIn], [IIa, IIa, IIc, IIe, IIj, IIl, IIn], [IIa, IIa, IIc, IIe, IIj, IIm, IIn], [IIa, IIa, IIc, IIe, IIk, IIl, IIn], [IIa, IIa, IIc, IIe, IIk, IIm, IIn], [IIa, IIa, IIc, IIf, IIh, IIl, IIn], [IIa, IIa, IIc, IIf, IIh, IIm, IIn], [IIa, IIa, IIc, IIf, IIi, IIl, IIn], [IIa, IIa, IIc, IIf, IIi, IIm, IIn], [IIa, IIa, IIc, IIf, IIj, IIl, IIn], [IIa, IIa, IIc, IIf, IIj, IIm, IIn], [IIa, IIa, IIc, IIf, IIk, IIl, IIn], [IIa, IIa, IIc, IIf, IIk, IIm, IIn], [IIa, IIa, IIc, IIg, IIh, IIl, IIn], [IIa, IIa, IIc, IIg, IIh, IIm, IIn], [IIa, IIa, IIc, IIg, IIi, IIl, IIn], [IIa, IIa, IIc, IIg, IIi, IIm, IIn], [IIa, IIa, IIc, IIg, IIj, IIl, IIn], [IIa, IIa, IIc, IIg, IIj, IIm, IIn], [IIa, IIa, IIc, IIg, IIk, IIl, IIn], [IIa, IIa, IIc, IIg, IIk, IIm, IIn], [IIa, IIa, IId, IIe, IIh, IIl, IIn], [IIa, IIa, IId, IIe, IIh, IIm, IIn], [IIa, IIa, IId, IIe, IIi, IIl, IIn], [IIa, IIa, IId, IIe, IIi, IIm, IIn], [IIa, IIa, IId, IIe, IIj, IIl, IIn], [IIa, IIa, IId, IIe, IIj, IIm, IIn], [IIa, IIa, IId, IIe, IIk, IIl, IIn], [IIa, IIa, IId, IIe, IIk, IIm, IIn], [IIa, IIa, IId, IIf, IIh, IIl, IIn], [IIa, IIa, IId, IIf, IIh, IIm, IIn], [IIa, IIa, IId, IIf, IIi, IIl, IIn], [IIa, IIa, IId, IIf, IIi, IIm, IIn], [IIa, IIa, IId, IIf, IIj, IIl, IIn], [IIa, IIa, IId, IIf, IIj, IIm, IIn], [IIa, IIa, IId, IIf, IIk, IIl, IIn], [IIa, IIa, IId, IIf, IIk, IIm, IIn], [IIa, IIa, IId, IIg, IIh, IIl, IIn], [IIa, IIa, IId, IIg, IIh, IIm, IIn], [IIa, IIa, IId, IIg, IIi, IIl, IIn], [IIa, IIa, IId, IIg, IIi, IIm, IIn], [IIa, IIa, IId, IIg, IIj, IIl, IIn], [IIa, IIa, IId, IIg, IIj, IIm, IIn], [IIa, IIa, IId, IIg, IIk, IIl, IIn], [IIa, IIa, IId, IIg, IIk, IIm, IIn].

Substituents groups (IIIa) to (IIIn) are shown as preferable substituent(s) groups for R⁶to R⁸, R^E, and Z of the compound represented by general formula (III)

For R⁶and R⁷, (IIIa) each independently a halogen atom.

For R⁸, (IIIb) a halogen atom, C1-C3 alkyl, or C1-C3 alkyloxy, (IIIc) C1-C3 alkyl or C1-C3 alkyloxy, (IIId) C1-C3 alkyl.

For R^E, (IIIe) C1-C15 alkyl substituted with one substituent selected from substituent group consists of (C1-C8 alkyloxy and C1-C4 alkyloxy-C2-C4 alkyloxy), C2-C15 alkynyl substituted with one substituent selected from substituent group consists of (C1-C8 alkyloxy and C1-C4 alkyloxy-C2-C4 alkyloxy), or C1-C15 alkyloxy substituted with one substituent selected from substituent group consists of (C1-C8 alkyloxy and C1-C4 alkyloxy-C2-C4 alkyloxy), (IIIf) C1-C15 alkyl substituted with one C1-C8 alkyloxy, C2-C15 alkynyl substituted with one C1-C8 alkyloxy, or C1-C15 alkyloxy substituted with one C1-C8 alkyloxy, (IIIg) C1-C15 alkyl substituted with one C1-C4 alkyloxy-C2-C4 alkyloxy, C2-C15 alkynyl substituted with one C1-C4 alkyloxy-C2-C4 alkyloxy, or C1-C15 alkyloxy substituted with one C1-C4 alkyloxy-C2-C4 alkyloxy.

For Z, (IIIh) ethylene or oxymethylene, (IIIi) ethylene.

Examples of preferable group of the compound represented by general formula (III) contains [R⁶, R⁷, R⁸, R^E, Z]=[IIIa, IIIa, IIIb, IIIe, IIIh], [IIIa, IIIa, IIIb, IIIe, IIIi], [IIIa, IIIa, IIIb, IIIf, IIIh], [IIIa, IIIa, IIIb, IIIf, IIIi], [IIIa, IIIa, IIIb, IIIg, IIIh], [IIIa, IIIa, IIIb, IIIg, IIIi], [IIIa, IIIa, IIIc, IIIe, IIIh], [IIIa, IIIa, IIIc, IIIe, IIIi], [IIIa, IIIa, IIIc, IIIf, IIIh], [IIIa, IIIa, IIIc, IIIf, IIIi], [IIIa, IIIa, IIIc, IIIg, IIIh], [IIIa, IIIa, IIIc, IIIg, IIIi], [IIIa, IIIa, IIId, IIIe, IIIh], [IIIa, IIIa, IIId, IIIe, IIIi], [IIIa, IIIa, IIId, IIIf, IIIh], [IIIa, IIIa, IIId, IIIf, IIIi], [IIIa, IIIa, IIId, IIIg, IIIh], [IIIa, IIIa, IIId, IIIg, IIIi].

Substituents groups (II-Aa) to (II-Al) are shown as preferable substituent(s) groups for R⁶to R⁸, R^C, R^D, and R^Fof the compound represented by general formula (II-A)

For R⁶and R⁷, (II-Aa) each independently a halogen atom.

For R⁸, (II-Ab) a halogen atom, C1-C3 alkyl, or C1-C3 alkyloxy, (III-Ac) C1-C3 alkyl or C1-C3 alkyloxy, (II-Ad) C1-C3 alkyl.

For R^C, (II-Ae) a halogen atom or C1-C6 alkyloxy, (III-Af) halogen atom, (II-Ag) C1-C6 alkyloxy.

For R^D, (II-Ah) a hydrogen atom or C1-C3 alkyloxy, (II-Ai) a hydrogen atom.

For R^F, (II-Aj) C1-C14 alkyl substituted with one substituent selected from substituent group consists of (C1-C8 alkyloxy and C1-C4 alkyloxy-C2-C4 alkyloxy), C2-C14 alkynyl substituted with one substituent selected from substituent group consists of (C1-C8 alkyloxy and C1-C4 alkyloxy-C2-C4 alkyloxy), or C1-C 14 alkyloxy substituted with one substituent selected from substituent group consists of (C1-C8 alkyloxy and C1-C4 alkyloxy-C2-C4 alkyloxy), (II-Ak) C1-C14 alkyl substituted with one C1-C8 alkyloxy, C2-C14 alkynyl substituted with one C1-C8 alkyloxy, or C1-C14 alkyloxy substituted with one C1-C8 alkyloxy, (II-Al) C1-C14 alkyl substituted with one C1-C4 alkyloxy-C2-C4 alkyloxy, C2-C14 alkynyl substituted with one C1-C4 alkyloxy-C2-C4 alkyloxy, or C1-C14 alkyloxy substituted with one C1-C4 alkyloxy-C2-C4 alkyloxy.

Examples of preferable group of the compound represented by general formula (II-A) contains [R⁶, R⁷, R⁸, R^C, R^D, R^F]=[II-Aa, II-Aa, II-Ab, II-Ae, II-Ah, II-Aj], [II-Aa, II-Aa, II-Ab, II-Ae, II-Ah, II-Ak], [II-Aa, II-Aa, II-Ab, II-Ae, II-Ah, II-Al], [II-Aa, II-Aa, II-Ab, II-Ae, II-Ai, II-Aj], [II-Aa, II-Aa, II-Ab, II-Ae, II-Ai, II-Ak], [II-Aa, II-Aa, II-Ab, II-Ae, II-Ai, II-Al], [II-Aa, II-Aa, II-Ab, II-Af, II-Ah, II-Aj], [II-Aa, II-Aa, II-Ab, II-Af, II-Ah, II-Ak], [II-Aa, II-Aa, II-Ab, II-Af, II-Ah, II-Al], [II-Aa, II-Aa, II-Ab, II-Af, II-Ai, II-Aj], [II-Aa, II-Aa, II-Ab, II-Af, II-Ai, II-Ak], [II-Aa, II-Aa, II-Ab, II-Af, II-Ai, II-Al], [II-Aa, II-Aa, II-Ab, II-Ag, II-Ah, II-Aj], [II-Aa, II-Aa, II-Ab, II-Ag, II-Ah, II-Ak], [II-Aa, II-Aa, II-Ab, II-Ag, II-Ah, II-Al], [II-Aa, II-Aa, II-Ab, II-Ag, II-Ai, II-Ak], [II-Aa, II-Aa, II-Ab, II-Ag, II-Aj, II-Al], [II-Aa, II-Aa, II-Ac, II-Ae, II-Ah, II-Aj], [II-Aa, II-Aa, II-Ac, II-Ae, II-Ah, II-Ak], [II-Aa, II-Aa, II-Ac, II-Ae, II-Ah, II-Al], [II-Aa, II-Aa, II-Ac, II-Ae, II-Ai, II-Aj], [II-Aa, II-Aa, II-Ac, II-Ae, II-Ai, II-Ak], [II-Aa, II-Aa, II-Ac, II-Ae, II-Ai, II-Al], [II-Aa, II-Aa, II-Ac, II-Af, II-Ah, II-Aj], [II-Aa, II-Aa, II-Ac, II-Af, II-Ah, II-Ak], [II-Aa, II-Aa, II-Ac, II-Af, II-Ah, II-Al], [II-Aa, II-Aa, II-Ac, II-Af, II-Aj, II-Aj], [II-Aa, II-Aa, II-Ac, II-Af, II-Aj, II-Ak], [II-Aa, II-Aa, II-Ac, II-Af, II-Aj, II-Al], [II-Aa, II-Aa, II-Ac, II-Ag, II-Ah, II-Aj], [II-Aa, II-Aa, II-Ac, II-Ag, II-Ah, II-Ak], [II-Aa, II-Aa, II-Ac, II-Ag, II-Ah, II-Al], [II-Aa, II-Aa, II-Ac, II-Ag, II-Ai, II-Aj], [II-Aa, II-Aa, II-Ac, II-Ag, II-Ai, II-Ak], [II-Aa, II-Aa, II-Ac, II-Ag, II-Ai, II-Al], [II-Aa, II-Aa, II-Ad, II-Ae, II-Ah, II-Aj], [II-Aa, II-Aa, II-Ad, II-Ae, II-Ah, II-Ak], [II-Aa, II-Aa, II-Ad, II-Ae, II-Ah, II-Al], [II-Aa, II-Aa, II-Ad, II-Ae, II-Ai, II-Aj], [II-Aa, II-Aa, II-Ad, II-Ae, II-Ai, II-Ak], [II-Aa, II-Aa, II-Ad, II-Ae, II-Ai, II-Al], [II-Aa, II-Aa, II-Ad, II-Af, II-Ah, II-Aj], [II-Aa, II-Aa, II-Ad, II-Af, II-Ah, II-Ak], [II-Aa, II-Aa, II-Ad, I-Af, II-Ah, II-Al], [II-Aa, II-Aa, II-Ad, II-Af, II-AJ, II-Aj], [II-Aa, II-Aa, II-Ad, II-Af, II-Aj, I-Ak], [II-Aa, II-Aa, II-Ad, II-Af, II-Aj, II-Al], [II-Aa, II-Aa, II-Ad, II-Ag, II-Ah, II-Aj], [II-Aa, II-Aa, II-Ad, II-Ag, II-Ah, II-Ak], [II-Aa, II-Aa, II-Ad, II-Ag, II-Ah, II-Al], [II-Aa, II-Aa, II-Ad, II-Ag, II-Ai, II-Aj], [II-Aa, II-Aa, II-Ad, II-Ag, II-Ai, II-Ak], [II-Aa, II-Aa, II-Ad, II-Ag, II-Ai, II-Al], [II-Aa, II-Aa, II-Ad, II-Ag, II-Ai, II-Al].

In the present specification, the term “platelet production modifier” means pharmaceutical composition for hemopathy accompanied with the unusual number of platelet. For example the hemopathy is thrombocytopenia (thrombocytopenia after bone marrow transplantation, chemotherapy-indeuced thrombocytopenia, Aplastic anemia, myelodysplasia syndrome, acquired thrombopenia such as idiopathic thrombopoietinic purpura, congenital amegakaryocytic thrombocytopenia such as thrombopoietin deficiency), and the like. For example this medicine can be used as treating agent in the case of decreacing number of platelet by administrating antitumor agent, or as protecting agent in the case of expecting the decreace of number of platelet by administrating antitumor agent.

In the present specification, the term “modifiering a platelet production” means 1) increasing a number of platelet decreased by administrating antitumor agent and the like. 2) maintaining a number of platelet which may be decreased by administrating antitumor agent and the like. 3) reducing the ratio of the platelet number of decrease caused by administrating antitumor agent and the like.

BEST MODE FOR CARRYING OUT THE INVENTION

Compounds (I) of the invention can be synthesized by the following methods A to B and the similar process.
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wherein R⁶, R⁷, R⁸, and R⁹are as defined above mentioned; R^Land R^Mare a protecting group; X¹is a group represented by the formula (IX), M is alkali metal.

wherein R¹, R², R³, R⁴, and R⁵are as defined above mentioned.

(Step 1)

This step is a process of preparing the compound (V) by protecting of a carboxyl group of 4-formylbenzoic acid derivatives (IV) by R^L. In step 3 conbination of R^Land R^Mis important in order to remove selectively protecting groups of two carboxylic acid. In the case of R^Lis a protecting group such as methyl and ethyl, which can be removed by basic condition, it is necessary that a protecting group of R^Mcan be removed by another condition except basic condition. Examples of R^Mare allyl (removed by palladium (0) complex), tert-butyl, p-methyloxybenzyl, triphenylmethyl, diphenylmethyl (removed by acidic condition), trimethylsilylethyl, trimethylsilylethoxymethyl, tert-butyldimethylsilyl (removed by fluoride ion) and the like.

Esterification condition can be used the method of reacting with considerable halocompound in the presence of suitable base. And it can be synthesized by condensation reaction using an alcohol derivative as starting material.

(Step 2)

This step is a process of preparing the compound (VI) by converting an aldehyde group of the compound (V) to olefin. For examples, the olefin can be syntesized by the reaction using phosphineylide such as Wittig reaction, Horner-Emmons reaction, or by dehydrated condensation reaction such as Knoevenagel reaction.

(Step 3)

This step is a process of preparing the compound (VII) removing the protecting group R^Lof the compound (VI). The removal of protecting group R^Lis carried out under suitable reaction condition as described in Protective Groups in Organic Synthesis, Theodora W Green (John Wiley & Sons).

(Step 4)

This step is a process of preparing amide the compound (VIII) or the compound (I-A wherein R^Mis C1-C4 alkyl) from the compound (VII) and an amine derivative (X¹—NH₂) by the method such as active esterification, acid chloride, mixed acid anhydride. This step is reacted in the solvent such as tetrahydrofuran, dioxane, dichloromethane, toluene, benzene. At active esterification method it can be carried out by using 1-hydroxybenzotriazole, hydroxysuccinimide, dimethylaminopyridine, and the like and dicyclohexylcarbodiimide, 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride salt, and the like as condensation reagent. At acid halide method it can be carried out by converting free carboxylic acid which is reacted with thionyl chloride or oxalyl chloride to acid chloride. At mixed acid anhydride method it can be carried out by converting carboxylic acid which is reacted with ethylchloroformate, isobutylchloroformate or the like to mixed acid anhydride. Triethylamine, pyridine or the like are used as base in these reaction according to be necessary.

(Step 5)

This step is a process of preparing the compound (I-B) by removing a protecting group R^Mof the compound (VIII) or the compound (I-A). The protecting group R^Mis removed under suitable reaction condition by using the method as described in Protective Groups in Organic Synthesis, Theodora W Green (John Wiley & Sons).

(Step 6)

This step is a process of preparing the compound (I-A) by alkylating the compound (I-B). This step is reacted in the solvent such as tetrahydrofuran, dioxane, dichloromethane, toluene, N,N-dimethylformamide. At alkylation method it can be carried out by condensation with C1-C6 alkyl halide in the presence of base such as potassium carbonate, sodium hydride. At acid chloride method it can be carried out by converting free carboxylic acid which is reacted with thionyl chloride or oxalyl chloride to acid chloride, and then was reacted with C1-C6 alcohol. Triethylamine, pyridine or the like are used as base in these reaction according to be necessary.

(Step 7)

This step is a process of preparing the compound (I-C) by treating the compound (I-B) with alkali metal such as sodium, potassium or alkali metal hydroxide. This step is reacted in the solvent such as tetrahydrofuran, dioxane, dichloromethane, toluene, N,N-dimethylformamide, alcohol such as methanol, ethanol, and the like in the presence of base such as alkali metal such as sodium, potassium or alkali metal hydroxide.

(Method B)

This method is another method for preparing the compound (VIII) or the compound (I-A) as described method A.
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wherein R⁶, R⁷, R⁸, R^M, and X¹are as defined above mentioned.

(Step 1)

This step is a process of preparing the compound (X) in a manner similar to Step 4 of Method A.

(Step 2)

This step is a process of preparing the compound (VIII) or the compound (I-A) by converting an aldehyde group of the compound (X) to olefin in a manner similar to Step 2 of Method A.

(Method C)

This method is another method for preparing the compound (VIII) or the compound (I-A) as described method A.
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wherein R⁶, R⁷, R⁸R^M, and X¹are as defined above mentioned.

(Step 1)

This step is a process of preparing the compound (XII) by converting an aldehyde group of the compound (XI) to olefin group in a manner similar to Step 2 of Method A.

(Step 2)

This step is a process of preparing the compound (VIII) or the compound (I-A) by substituting a bromo group of the compound (XII). At this step it can be carried out by adding carbon monoxide to a DMF solution of the compound (XII) and X¹NH₂in the presence of dichlorobistriphenylphosphinepalladium and base such as triethylamine. The reaction temperature is used 20° C. to 120° C., preferably 50° C. to 100° C. The reaction time is used 1 h to 48 h, preferably 4 h to 24 h.

The term “solvate” includes, for example, solvates with organic solvents, hydrates, and the like.

The term “compound of the present invention” herein used includes a pharmaceutically acceptable salt or solvate thereof. The salt is exemplified by a salt with alkali metals (e.g., lithium, sodium, potassium, and the like), alkaline earth metals (e.g., magnesium, calcium, and the like), ammonium, organic bases, amino acids, mineral acids (e.g., hydrochloric acid, hydrobromic acid, phosphoric acid, sulfuric acid, and the like), or organic acids (e.g., acetic acid, citric acid, maleic acid, fumaric acid, benzenesulfonic acid, p-toluenesulfonic acid, and the like). These salts can be formed by the usual method. These hydrates can coordinate with any water molecules when hydrates are formed.

Prodrug is a derivative of the compound having a group which can be decomposed chemically or metabolically, and such prodrug is a compound according to the present invention which becomes pharmaceutically active by means of solvolysis or by placing the compound in vivo under a physiological condition. The method of both selection and manufacture of appropriate prodrug derivatives is described in, for example. Design of Prodrugs, Elsevier, Amsterdam, 1985). For instance, prodrugs such as an ester derivative which is prepared by reacting a basal acid compound with a suitable alcohol, or an amide derivative which is prepared by reacting a basal acid compound with a suitable amine are exemplified when the compounds according to present invention have a carboxylic group. Particularly preferred esters as prodrugs are methyl ester, ethyl ester, n-propyl ester, isopropyl ester, n-butyl ester, isobutyl ester, tert-butyl ester, morpholinoethyl ester, and N,N-diethylglycolamido ester, and the like. For instance, when the compounds according to present invention have a hydroxy group, prodrugs such as an acyloxy derivative which is prepared by reacting with a suitable acyl halide or a suitable acid anhydride. Particularly preferred acyloxy derivatives as prodrugs —OCOC₂H₅, —OCO(t-Bu), —OCOC₁₅H₃₁, —OCO(m-COONa-Ph), —COCH₂CH₂COONa, —OCOCH(NH₂)CH₃, —OCOCH₂N(CH₃)₂, and the like. For instance, when the compounds according to present invention have an amino group, prodrugs such as an amide derivative which is prepared by reacting with a suitable acid halide or a suitable acid anhydride. Particularly preferred amide as prodrugs are —NHCO(CH₂)₂₀CH₃, —NHCOCH(NH₂)CH₃, and the like.

The compound of the present invention is not restricted to any particular isomers but includes all possible isomers and racemic modifications.

The present invention compounds show excellent thrombopoietin receptor agonism as described in examples mentioned later, and may be used as a pharmaceutical composition (platelet production modifier) for hemopathy accompanied with the unusual number of platelet, for example thrombocytopenia (e.g., thrombocytopenia after bone marrow transplantation, chemocherapy-indeuced thrombocytopenia, Aplastic anemia, myelodysplastic syndrome, acquired thrombocytopenia such as idiopathic thrombocytopenic purpura, congenital amegakaryocytic thrombocytopenia such as thrombopoietin deficiency), and the like. And the present compound may be used as treating and/or preventing agent for the unusual number of platelet accompanied with administering antitumor agent.

When the compound of the present invention is administered to a person for the treatment of the above diseases, it can be administered orally as powder, granules, tablets, capsules, pilulae, and liquid medicines, or parenterally as injections, suppositories, percutaneous formulations, insufflation, or the like. An effective dose of the compound is formulated by being mixed with appropriate medicinal admixtures such as excipient, binder, penetrant, disintegrators, lubricant, and the like if necessary. Parenteral injections are prepared by sterilizing the compound together with an appropriate carrier.

The dosage varies with the conditions of the patients, administration route, their age, and body weight. In the case of oral administration, the dosage can generally be between 0.1 to 100 mg/kg/day, and preferably 1 to 20 mg/kg/day for adult.

The following examples are provided to further illustrate the present invention and are not to be constructed as limiting the scope thereof.

Abbreviations described below are used in the following examples.

Me: methyl
Et: ethyl
n-Bu: n-butyl
Ph: phenyl
Tf: trifluoromethanesulfonyl
DMF: N,N-dimethylformamide
THF: tetrahydrofuran

EXAMPLES
Example 1
Synthesis of Compound (A1)

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1) Synethesis of 4-bromo-2,6-difluorobenzaldehyde (2)

To a THF (250 mL) solution of diisopropylamine (53 mL) was added 2.44 M hexane solution of butyl lithium at −78° C., and the reaction mixture was stirred for 30 miniute. To the reaction mixture was added a THF solution of 3,5-difluorobromobenzene (1) (36 g), and then the reaction mixture was stirred for 1 h. To the reaction mixture was added DMF 146 mL, and the reaction mixture was stirred for additional 1 h. To the reaction mixture was added a saturated ammonium chloride aqueous solution, and the reaction mixture was extracted with ethyl acetate. The organic layer was washed with water, and brine, dried over magnesium sulfate, and evaporated. The obtained residue was purified by column chromatography (hexane:ethyl acetate=20:1) to obtain the compoumd (2) 23.2 g.

¹H-NMR(CDCl₃) 10.29(s, 1H), 7.19-7.25(m, 2H).

2) Synthesis of ethyl 3-(4-bromo-2,6-difluorophenyl)-2-methylacrylate (3)

To a THF (100 mL) solution of triethyl-2-phosphonopropionic acid (33.8 mL) was added sodium hydride (8.4 g) under ice-cooling. After the reaction mixture was stirred for 1 h, to the reaction mixture was added a THF solution of 4-bromo-2,6-difluorobenzaldehyde (2) (23.2 g) dropwise under ice-cooling. After the reaction mixture was stirred under ice-cooling for 2 h, to the reaction mixture were added ice-water, 2N hydrochloric acid, and the reaction mixture was extracted with ethyl acetate. The organic layer was washed with water, and brine, dried over magnesium sulfate, and evaporated. The obtained residue was purified by column chromatography (hexane:ethyl acetate=15:1) to obtain the compoumd (3) 32.08 g.

¹H-NMR(CDCl₃) 7.32(d, 1H, J=1.5 Hz), 7.11-7.17(m, 2H), 4.28(q, 2H, J=7.2 Hz), 1.86(d, 3H, J=1.5 Hz), 1.35(t, 3H, J=7.2 Hz).

3) Synthesis of 5-(3-methyloxyhexyn-1-yl)tetralone (5)

To a DMF (100 mL) solution of 5-hydroxytetralone trifluoromethanesulfonic acid ester (4) (13.5 g), 3-methyloxy-1-hexyne (10.3 g), dichlorobistriphenylphosphinepalladium (0.9 g), and copper iodide (0.5 g) was added triethylamine (10 mL), and then the reaction mixture was stirred at 80° C. for 64 h. To the reaction mixture were added water, and the reaction mixture was extracted with ethyl acetate. The organic layer was washed with water, and brine, dried over magnesium sulfate, and evaporated. The obtained residue was purified by column chromatography (hexane:ethyl acetate=4:1) to obtain the compoumd (5) 11 g.

¹H-NMR(CDCl₃) 8.01(d, 1H, J=7.8 Hz), 7.62(dd, 1H, J=7.4 Hz, 1.4 Hz), 7.27(t, 1H, J=7.7 Hz), 4.23(t, 1H, J=6.6 Hz), 3.50(s, 3H), 3.11(t, 2H, J=6.1 Hz), 2.64-2.69(m, 2H), 2.14-2.21(m, 2H), 1.77-1.84(m, 2H), 1.52-1.60(m, 2H), 0.99(t, 3H, J=7.4 Hz),

4) Synthesis of 5-(3-methyloxyhexyl)tetralone (6)

To a THF (60 mL) solution of 5-(3-methyloxyhexyn-1-yl)tetralone (5) (11 g) was added 10% palladium-carbon (0.9 g), and the reaction mixture was stirred under a hydrogen gas atmosphere for 5 h. The reaction mixture filtered off, and the filtrate was evaporated. The obtained residue was purified by column chromatography (hexane:ethyl acetate=9:1) to obtain the compoumd (6) 9.0 g.

¹H-NMR(CDCl₃) 7.94(dd, 1H, J=7.8 Hz, 1.4 Hz), 7.36(dd, 1H, J=7.4 Hz, 1.4 Hz), 7.25(t, 1H, J=7.7 Hz), 3.37(s, 3H), 3.23-3.24(m, 1H), 2.91-2.96(m, 2H), 2.63-2.83(m, 4H), 2.05-2.17(m, 2H), 1.71-1.77(m, 2H), 1.26-1.59(m, 4H), 0.94(t, 3H, J=7.2 Hz).

5) Synthesis n of 4,5-dihydro-6-(3-methyloxyhexyl)naphtho[1,2-d]thiazol-2-ylamine (7)

To a 10% methanol-chloroform (60 mL) solution of 5-(3-methyloxyhexyl)tetralone (6) (9.0 g) was added bromine (5.5 g), and the reaction mixture was stirred for 1 h. After the solvent was evaoprated, the residue was dissolved in ethanol (60 mL), and to the residue was added thiourea (2.65 g). After the mixture was heated at reflux for 7 h, the reaction solvent was evported. To the residue was added a saturated sodium hydrogencarbonate aqueous solution, and the mixture was extracted with ethyl acetate. The organic layer was dried over magnesium sulfate, and evaporated. The obtained residue was purified by column chromatography (hexane:ethyl acetate=4:1) to obtain the compoumd (7) 4.6 g.

¹H-NMR(CDCl₃) 7.59(d, 1H, J=7.5 Hz), 7.17(t, 1H, J=7.7 Hz), 7.05(d, 1H, J=7.7 Hz), 4.93(bs, 2H), 3.36(s, 3H), 3.21(t, 1H, J=5.8 Hz), 2.99-3.05(m, 2H), 2.63-2.87(m, 4H), 1.68-1.76(m, 4H), 1.35-1.56(m, 4H), 0.93(t, 3H, J=7.2 Hz).

6) Synthesis of ethyl 3-{2,6-difluoro-4-[4,5-dihydro-6-(3-methyloxyhexyl)naphtho[1,2-d]thiazol-2-ylcarbamoyl]phenyl}-2-methylacrylate (8)

To a DMF (25 mL) solution of 4,5-dihydro-6-(3-methyloxyhexyl)naphtho[1,2-d]thiazol-2-ylamine (7) (4.5 g), 3-(4-bromo-2,6-difluorophenyl)-2-methylacrylic acid ethyl ester (3) (4.35 g), and dichlorobistriphenylphosphinepalladium (0.8 g) was added triethylamine (10 mL), and the reaction mixture was stirred under carbon monoxide atomosphere at 85° C. for 16 h. To the reaction mixtre was added water, and the reaction mixture was extracted with ethyl acetate. The organic layer was washed with water, and brine, dried over magnesium sulfate, and evaporated. The obtained residue was purified by column chromatography (hexane:ethyl acetate=4:1) to obtain the compoumd (8) 7.1 g.

¹H-NMR(CDCl₃) 7.36-7.38(m, 3H), 7.25(bs, 1H), 7.00(d, 2H, J=2.3 Hz), 4.29(q, 2H, J=7.2 Hz), 3.38(s, 3H), 3.22(t, 1H, J=5.5 Hz), 3.01-3.05(m, 4H), 2.60-2.80(m, 2H), 1.80(s, 3H), 1.67-1.75(m, 2H), 1.24-1.60(m, 7H), 0.94(t, 3H, J=7.2 Hz).

7) Synthesis of 3-{2,6-difluoro-4-[4,5-dihydro-6-(3-methyloxyhexyl)naphtho[1,2-d]thiazol-2-ylcarbamoyl]phenyl}-2-methylacrylic acid (A1)

A mixture of THF (40 mL), methanol (40 mL), and 2N sodium hydroxide aqueous solution (40 mL) of 3-{2,6-difluoro-4-[4,5-dihydro-6-(3-methyloxyhexyl)naphtho[1,2-d]thiazol-2-ylcarbamoyl]phenyl}-2-methylacrylic acid ethyl ester (8) (7.0 g), was stirred at room temperature for 3 h. The reaction mixture was acidified with hydrochloric acid, and extracted with ethyl acetate. The organic layer was washed with water, and brine, dried over magnesium sulfate, and evaporated. The residue was recrystallized from ethyl acetate to obtain the compound (A1) 5.5 g.

¹H-NMR(DMSO-d₆) 12.93(bs, 2H), 7.95(d, 2H, J=8.3 Hz), 7.64(d, 1H, J=7.5 Hz), 7.33(s, 3H), 7.09(d, 1H, J=6.7 Hz), 3.27(s, 3H), 3.21(t, 1H, J=6.3 Hz), 2.99(s, 4H), 2.60-2.80(m, 2H), 1.80(d, 3H, J=1.6 Hz), 1.64-1.66(m, 2H), 1.45-1.47(m, 2H), 1.31-1.33(m, 2H), 0.89(t, 3H, J=7.0 Hz).

Example 2
Synthesis of Compound (A1307)

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1) Synthesis of tert-butyl 3-(2-isopropylphenoxy)propionate (10)

2-Isopropylphenol (6 g) was dissolved in acrylic acid tert-butyl ester (6.2 g), and to the mixture was added potassium tert-butyloxide (0.3 g). The reaction mixture was stirred at 130° C. for 6 h. To the reaction mixture was added water, the reaction mixture extracted with ethyl acetate. The organic layer was washed with brine, dried over magnesium sulfate, and evaporated. The obtained residue was purified by column chromatography (hexane:ethyl acetate=9:1) to obtain the compound (10) 4.3 g.

¹H-NMR(CDCl3) 7.20(dd, 1H, J=7.5, 1.7 Hz), 7.14(dt, 1H, J=7.5, 1.7Hz), 6.92(dd, 1H, J=7.5, 1.7 Hz), 6.86(dt, 1H, J=7.5, 1.7 Hz), 4.21(t, 2H, J=6.3 Hz), 3.30(sext, 1H, J=7.0 Hz), 2.72(t, 2H, J=6.3 Hz), 1.45(s, 9H), 1.15(d, 6H, J=7.0 Hz).

2) Synthesis of 3-(2-isopropylphenoxy)propionic acid (11)

3-(2-Isopropylphenoxy)propionic acid tert-butyl ester (10) (4.3 g) was dissolved in dichloromethane (40 mL), and to the mixture was added trifluoroacetic acid (4 mL). The reaction mixture was stirred at room temperature for 3 h, and evaporated. The obtained residue was purified by column chromatography (hexane:ethyl acetate=4:1) to obtain the compound (11) 3.14 g.

¹H-NMR(CDCl3) 7.23(dd, 1H, J=7.5, 1.7 Hz), 7.17(dt, 1H, J=7.5, 1.7 Hz), 6.95(dd, 1H, J=7.5, 1.7 Hz), 6.89(dt, 1H, J=7.5, 1.7 Hz), 4.26(t, 2H, J=6.3 Hz), 3.30(sext, 1H, J=7.0 Hz), 2.78(t, 2H, J=6.3 Hz), 1.19(d, 6H, J=7.0 Hz).

3) Synthesis of 8-isopropylchroman-4-one (12)

3-(2-Isopropylphenoxy)propionic acid (11) was dissolved in dichloromethane (30 mL), and to the mixture were added oxalyl chloride (2.1 g) and DMF (5 mL) under ice-cooling. The reaction mixture was stirred for 30 minutes and cooled at −20° C. To the reaction mixture was added aluminium chloride (4 g), and the reaction mixture was stirred at −20° C. for 2 h. To the reaction mixture was added 2N hydrochloric acid, and the reaction mixture was extracted with dicloromethane. The organic layer was washed with brine, dried over magnesium sulfate, and evaporated. The obtained residue was purified by column chromatography (hexane:ethyl acetate=4:1) to obtain the compound (12) 2.3 g.

¹H-NMR(CDCl3) 7.73(d, 1H, J=7.5 Hz), 7.37(d, 1H, J=7.5 Hz), 6.93(t, 1H, J=7.5 Hz), 4.56(t, 2H, J=6.3 Hz), 3.25(sext, 1H, J=7.0 Hz), 2.78(t, 2H, J=6.3 Hz), 1.24(d, 6H, J=7.0 Hz).

4) Synthesis of 6-isopropyl-4H-chromeno[4,3-d]thiazol-2-ylamine (13)

8-Isopropylchroman-4-one (12) (2.3 g) was dissloved with 10% methanol-chloroform (20 mL), and to the mixture was added bromine (1.93 g). After the reaction mixture was stirred for 1 h, and evaporated. The residue was dissolved in ethanol (30 mL), and to the reaction mixture was added thiourea (0.92 g). The reaction mixture was heated at reflux, and evaporated. The residue was extracted with ethyl acetate, and a saturated sodium hydrogencarbonate aqueous solution, and the organic layer was dried over magnesium sulfate, and evaporated. The residue was purified by column chromatography (hexane:ethyl acetate=4:1) to obtain the compound (13) 0.7 g.

1H-NMR(CDCl3) 7.43(d, 1H, J=7.5 Hz), 7.10(d, 1H, J=7.5 Hz), 6.95(t, 1H, J=7.5 Hz), 5.29(s, 2H), 5.20(bs, 2H), 3.25(sext, 1H, J=7.0 Hz), 1.24(d, 6H, J=7.0 Hz)

5) (E)-3-[2,6-difluoro-4-(6-isopropyl-4H-chromeno[4,3-d]thiazol-2-ylcarbamoyl)phenyl]-2-methylacrylic acid ethyl ester(14)

6-Isopropyl-4H-chromeno[4,3-d]thiazol-2-ylamine (13) (360 mg), (Z)-3-(4-bromo-2,6-difluorophenyl)-2-methylacrylic acid ethyl ester (460 mg), and dichlorobistriphenylphosphinepalladium (150 mg) were dissolved in DMF (6 mL). To the mixture was poured triethylamine (0.84 mL), and the reaction mixture was stirred under carbon monoxide atomospher at 85° C. for 16 h. The reaction mixture was added into water, and extracted with ethyl acetate. The organic layer was washed with water, and brine, and dried over magnesium sulfate, and evaporated. The residue was purified by column chromatography (hexane:ethyl acetate=4:1) to obtain the compound (14) 620 mg.

1H-NMR(CDCl3) 7.44(s, 1H), 7.42(s, 1H), 7.28-7.33(m, 1H), 7.10(d, 1H, J=7.6 Hz), 6.85(t, 1H, J=7.6 Hz), 5.49(s, 2H), 4.27(q, 2H, J=7.0 Hz), 3.25(sext, 1H, J=7.0 Hz), 1.79(s, 3H), 1.25(t, 3H, J=7.0 Hz), 1.20(d, 6H, J=7.0 Hz).

6) (E)-3-[2,6-difluoro-4-(6-isopropyl-4H-chromeno[4,3-d]thiazol-2-ylcarbamoyl)phenyl]-2-methylacrylic acid (A1309)

(E)-3-[2,6-difluoro-4-(6-isopropyl-4H-chromeno[4,3-d]thiazol-2-ylcarbamoyl)phenyl]-2-methylacrylic acid ethyl ester (620 mg) was dissolved in THF (2 mL), methanol (2 ml), and 2N sodium hydroxide aqueous solution (2 mL), and the reaction mixture was stirred at room temperature for 3 h. The reaction mixture was acidified with hydrochloric acid and extracted with ethyl acetate. The organic layer was washed with water, and brine, dried over magnesium sulfate, and evaporated. The residue was recrystallized from ethyl acetate to obtain the compound (A1309) 460 mg.

1H-NMR(DMSO-d6) 12.93(bs, 1H), 7.98(s, 1H), 7.97(s, 1H), 7.48(d, 1H, J=7.6 Hz), 7.33(s, 1H), 7.11(d, 1H, J=7.6 Hz), 7.01(t, 1H, J=7.6 Hz ), 5.49(s, 2H), 3.20-3.30(m, 1H), 1.79(s, 3H), 1.04(d, 6H, J=6.0 Hz).

A2-A12, A339, A341, A346, A347, A349, A351, A401, A423, A430, A440, A450, A500, A601, A928, A930, A936, A937, A939, A941, A944, A954, A993, A1003, A1016, A1018, A1033, A1123, A1295-A1308, and A1310-A1332 were synthesized by similar method described above.

Example 3
Synthesis of 3-[2,6-difluoro-4-(4,5-dihydro-6-pentylnaphtho[1,2-d]thiazol-2-ylcabamoyl)phenyl]-2-methylacrylic acid (A2)

1H-NMR(DMSO-d6) 12.92(bs, 2H), 7.91-7.98(m, 2H), 7.62-7.65(m, 1H), 7.33(s, 1H), 7.18-7.23(m, 1H), 7.06-7.10(m, 1H), 2.97(s, 4H), 2.63(t, 2H, J=7.6 Hz), 1.80(s, 3H), 1.52(t, 2H, J=6.9 Hz), 1.32-1.35(m, 4H), 0.88(t, 3H, J=6.0 Hz).

Example 4
Synthesis of 3-{2,6-difluoro-4-[4,5-dihydro-6-(3,3-dimethylbutyl)naphtho[1,2-d]thiazol-2-ylcabamoyl)phenyl]-2-methylacrylic acid (A3)

1H-NMR(DMSO-d6) 12.96(bs, 2H), 7.92(d, 2H, J=8.1 Hz), 7.60(d, 1H, J=7.5 Hz), 7.30(s, 1H), 7.17(d, 1H, J=7.5 Hz), 7.03-7.06(m, 1H), 2.94(s, 4H), 2.53-2.59(m, 2H), 1.77(s, 3H), 1.31-1.37(m, 2H), 0.91(s, 9H).

Example 5
Synthesis of 3-{2,6-difluoro-4-[4,5-dihydro-6-(3-methyloxy-4,4-dimethylpentyl)naphtho[1,2-d]thiazol-2-ylcabamoyl]phenyl}-2-methylacrylic acid (A4)

1H-NMR(DMSO-d6) 12.91(bs, 1H), 7.95(d, 2H, J=7.6 Hz), 7.63(d, 1H, J=7.6 Hz), 7.33(d, 1H, J=1.3 Hz), 7.21(t, 1H, J=7.6 Hz), 7.09(d, 1H, J=7.6 Hz), 3.33(s, 3H), 3.21-3.26(m, 1H), 2.95-2.99(m, 4H), 2.65-2.70(m, 2H), 1.80(d, 3H, J=1.3 Hz), 1.70-1.80(m, 2H), 0.88(s, 9H).

Example 6
Synthesis of 3-{4-[6-(3-n-butyloxypropyl)-4,5-dihydronaphto[1,2-d]thiazol-2-ylcabamoyl]-2,6-difluorophenyl}-2-methylacrylic acid (A5)

1H-NMR(DMSO-d6) 12.94(bs, 1H), 7.94(d, 2H, J=7.6 Hz), 7.64(d, 1H, J=7.6 Hz), 7.33(d, 1H, J=1.3 Hz), 7.21(t, 1H, J=7.6 Hz), 7.05(d, 1H, J=7.6 Hz), 3.33-3.40(m, 4H), 2.95-2.99(m, 4H), 2.65(t, 2H, J=7.6 Hz), 1.88(d, 3H, J=1.3 Hz), 1.70-1.80(m, 2H), 1.45-1.53(m, 2H), 1.31-1.40(m, 2H), 0.89(t, 3H, J=7.4 Hz).

Example 7
Synthesis of 3-(2,6-difluoro-4-{4,5-dihydro-6-[3-(2,2-dimethylpropyloxy)propyl]naphtho[1,2-d]thiazol-2-ylcabamoyl}phenyl)-2-methylacrylic acid (A6)

1H-NMR(DMSO-d6) 12.93(bs, 1H), 7.95(d, 2H, J=7.6 Hz), 7.65(d, 1H, J=7.6 Hz), 7.33 (d, 1H, J=1.3 Hz), 7.21(t, 1H, J=7.6 Hz), 7.09(d, 1H, J=7.6 Hz), 3.40(t, 2H. J=6.4 Hz), 3.05(s, 2H), 2.95-2.99(m, 4H), 2.71(t, 2H, J=7.4 Hz), 1.84(d, 3H, J=1.3 Hz), 1.70-1.80(m, 2H), 0.91(s, 9H).

Example 8
Synthesis of 3-{2,6-difluoro-4-[4,5-dihydro-6-(3-isopropyloxypropyl)naphtho[1,2-d]thiazol-2-ylcabamoyl]phenyl}-2-methylacrylic acid (A7)

1H-NMR(DMSO-d6) 12.94(bs, 1H), 7.95(d, 2H, J=7.3 Hz), 7.65(d, 1H, J=7.3 Hz), 7.33(d, 1H, J=1.3 Hz), 7.21(t, 1H, J=7.3 Hz), 7.09(d, 1H, J=7.3 Hz), 3.53(hept, 1H, J=6.1 Hz), 3.40(t, 2H, J=6.4 Hz), 2.95-2.99(m, 4H), 2.69(t, 2H, J=7.0 Hz), 1.84(d, 3H, J=1.3 Hz), 1.75-1.80(m, 2H), 1.11(d, 6H, J=6.1 Hz).

Example 9
Synthesis of 3-{2,6-difluoro-4,5-dihydro-4-[6-(3-ethyloxypropyl)naphtho[1,2-d]thiazol-2-ylcabamoyl]phenyl}-2-methylacrylic acid (A8)

1H-NMR(DMSO-d6) 12.92(bs, 1H), 7.95(d, 2H, J=7.6 Hz), 7.64(d, 1H, J=7.6 Hz), 7.34(d, 1H, J=1.3 Hz), 7.21(t, 1H, J=7.6 Hz), 7.09(d, 1H, J=7.6 Hz), 3.33-3.40(m, 4H), 2.95-2.99(m, 4H), 2.71(t, 2H, J=7.0 Hz), 1.80(d, 3H, J=1.3 Hz), 1.70-1.80(m, 2H), 1.12(t, 3H, J=7.4 Hz).

Example 10
Synthesis of 3-{2,6-difluoro-4-[4,5-dihydro-6-(3-n-propyloxypropyl)naphto[1,2-d]thiazol-2-ylcabamoyl]phenyl}-2-methylacrylic acid (A9)

1H-NMR(DMSO-d6) 12.91(bs, 1H), 7.95(d, 2H, J=7.6 Hz), 7.65(d, 1H, J=7.6 Hz), 7.33 (d, 1H, J=1.3 Hz), 7.21(t, 1H, J=7.6 Hz), 7.09(d, 1H, J=7.6 Hz), 3.33-3.40(m, 4H), 2.95-2.99(m, 4H), 2.70(t, 2H, J=7.0 Hz), 1.80(d, 3H, J=1.3 Hz), 1.70-180(m, 2H), 1.45-1.53(m, 2H), 0.89(t, 3H, J=7.4 Hz).

Example 11
Synthesis of 3-{2,6-dichloro-4-[4,5-dihydro-6-(3-ethyloxypropyl)naphtho[1,2-d]thiazol-2-ylcabamoyl]phenyl}-2-methylacrylic acid (A10)

1H-NMR(DMSO-d6) 12.92(bs, 1H), 8.28(s, 2H), 7.64(d, 1H, J=7.6 Hz), 7.4(d, 1H, J=1.3 Hz), 7.21(t, 1H, J=7.6 Hz), 7.09(d, 1H, J=7.6 Hz), 3.33-3.40(m, 4H), 2.95-2.99(m, 4H), 2.71(t, 2H, J=7.0 Hz), 1.75-1.80(m, 2H), 1.70(d, 3H, J=1.3 Hz), 1.12(t, 3H, J=7.0 Hz).

Example 12
Synthesis of 3-{4-[6-(3-n-butyloxypropyl)-4,5-dihydronaphtho[1,2-d]thiazol-2-ylcabamoyl]-2,6-dichlorophenyl}-2-methylacrylic acid (A11)

1H-NMR(DMSO-d6) 12.91(bs, 1H), 8.27(s, 2H), 7.64(d, 1H, J=7.6 Hz), 7.40(d, 1H, J=1.3 Hz), 7.21(t, 1H, J=7.6 Hz), 7.09(d, 1H, J=7.6 Hz), 3.33-3.40(m, 4H), 2.95-2.99(m, 4H), 2.70(t, 2H, J=7.0 Hz), 1.75-1.80(m, 2H), 1.70(d, 3H, J=1.3 Hz), 1.52-1.58(m, 2H), 1.31-1.40(m, 2H), 0.89(t, 3H, J=7.0 Hz).

Example 13
Synthesis of 3-{2,6-difluoro-4-[4,5-dihydro-6-(3-methyloxyhexyl)naphtho[1,2-d]thiazol-2-ylcabamoyl]phenyl}-2-methylacrylic acid (A12)

1H-NMR(DMSO-d6) 12.97(bs, 1H), 8.27(s, 2H), 7.64(d, 1H, J=7.6 Hz), 7.40(d, 1H, J=1.3 Hz), 7.24(t, 1H, J=7.6 Hz), 7.09(d, 1H, J=7.6 Hz), 3.33(s, 3H), 3.21-3.26(m, 1H), 2.95-2.99(m, 4H), 2.65-2.70(m, 2H), 1.70(d, 3H, J=1.3 Hz), 1.65-1.70(m, 2H), 1.52-1.58(m, 2H), 1.31-1.40(m, 2H), 0.89(t, 3H, J=7.0 Hz).

Example 14
Synthesis of (E)-3-{2,6-difluoro-4-[6-(3-methyloxypentyl)-4,5-dihydronaphtho[1,2-d]thiazol-2-ylcabamoyl]phenyl}-2-methylacrylic acid (A339)

1H-NMR(DMSO-d6) 12.91(bs, 1H), 7.96(s, 1H), 7.93(s, 1H), 7.65(d, 1H, J=7.6 Hz), 7.33(s, 1H), 7.21(t, 1H, J=7.6 Hz), 7.09(d, 1H, J=7.6 Hz), 3.27(s, 3H), 3.10-3.16(m, 1H), 2.95-2.99(m, 4H), 2.65-2.80(m, 2H), 1.80(s, 3H), 1.60-1.70(m, 2H), 1.45-1.60(m, 2H), 0.86(t, 3H, J=7.6 Hz).

Example 15
Synthesis of (E)-3-{2,6-difluoro-4-[6-(3-methyloxyheptyl)-4,5-dihydronaphtho[1,2-d]thiazol-2-ylcabamoyl]phenyl}-2-methylacrylic acid (A341)

1H-NMR(DMSO-d6) 12.91(bs, 1H), 7.96(s, 1H), 7.93(s, 1H), 7.65(d, 1H, J=7.6 Hz), 7.33(s, 1H), 7.21(t, 1H, J=7.6 Hz), 7.09(d, 1H, J=7.6 Hz), 3.25(s, 3H), 3.14-3.22(m, 1H), 2.95-2.99(m, 4H), 2.50-2.65(m, 2H), 1.79(s, 3H), 1.60-1.69(m, 2H), 1.45-1.55(m, 2H), 1.22-1.34(m, 4H), 0.90-094(m, 3H).

Example 16
Synthesis of (E)-3-{4-[6-(3-ethyloxypentyl)-4,5-dihydronaphtho[1,2-d]thiazol-2-ylcabamoyl]-2,6-difluorophenyl}-2-methylacrylic acid (A346)

1H-NMR(DMSO-d6) 12.91(bs, 1H), 7.96(s, 1H), 7.94(s, 1H), 7.64(d, 1H, J=7.6 Hz), 7.33(s, 1H), 7.18(t, 1H, J=7.6 Hz), 7.09(d, 1H, J=7.6 Hz), 3.45(q, 2H, J=7.0 Hz), 3.20-3.26(m, 1H), 2.95-2.99(m, 4H), 2.60-2.80(m, 2H), 1.79(s, 3H), 1.60-1.69(m, 2H), 1.45-1.55(m, 2H), 1.13(t, 3H, J=7.0 Hz), 0.86(t, 3H, J=7.6 Hz).

Example 17
Synthesis of (E)-3-{4-[6-(3-ethyloxyhexyl)-4,5-dihydronaphtho[1,2-d]thiazol-2-ylcabamoyl]-2,6-difluorophenyl}-2-methylacrylic acid (A347)

1H-NMR(DMSO-d6) 12.91(bs, 1H), 7.96(s, 1H), 7.94(s, 1H), 7.64(d, 1H, J=7.6 Hz), 7.33(s, 1H), 7.20(t, 1H, J=7.6 Hz), 7.09(d, 1H, J=7.6 Hz), 3.45(q, 2H, J=7.0 Hz), 3.20-3.26(m, 1H), 2.95-2.99(m, 4H), 2.60-2.80(m, 2H), 1.79(s, 3H), 1.60-1.69(m, 2H), 1.45-1.55(m, 2H), 1.30-1.40(m, 2H), 1.13(t, 3H, J=7.0 Hz), 0.86(t, 3H, J=7.6 Hz).

Example 18
Synthesis of (E)-3-{4-[6-(3-ethyloxyheptyl)-4,5-dihydronaphtho[1,2-d]thiazol-2-ylcabamoyl]-2,6-difluorophenyl}-2-methylacrylic acid (A349)

1H-NMR(DMSO-d6) 12.91(bs, 1H), 7.96(s, 1H), 7.94(s, 1H), 7.64(d, 1H, J=7.6 Hz), 7.33(s, 1H), 7.20(t, 1H, J=7.6 Hz), 7.09(d, 1H, J=7.6 Hz), 3.48(q, 2H, J=7.0 Hz), 3.20-3.26(m, 1H), 2.95-2.99(m, 4H,), 2.60-2.80(m, 2H), 1.79(s, 3H), 1.60-1.69(m, 2H), 1.45-1.55(m, 2H), 1.30-1.40(m, 4H), 1.13(t, 3H, J=7.0 Hz), 0.86-0.89(m, 3H).

Example 19
Synthesis of (E)-3-{4-[6-(3-ethyloxy-4,4-dimethylpentyl)-4,5-dihydronaphtho[1,2-d]thiazol-2-ylcabamoyl]-2,6-difluorophenyl}-2-methylacrylic acid (A351)

1H-NMR(DMSO-d6) 12.95(bs, 1H), 7.96(s, 1H), 7.93(s, 1H), 7.65(d, 1H, J=7.6 Hz), 7.33 (s, 1H), 7.23(t, 1H, J=7.6 Hz), 7.09(d, 1H, J=7.6 Hz), 3.50-3.65(m, 2H), 2.95-2.99(m, 4H), 2.80-2.90(m, 2H), 2.59-2.65(m, 1H), 1.80(s, 3H), 1.60-1.70(m, 1H), 1.45-1.5 (m, 1H), 1.17(t, 3H, J=7.0 Hz), 0.90(s, 9H).

Example 20
Synthesis of (E)-3-{2,6-difluoro-4-[6-(3-pentyloxypropyl)-4,5-dihydronaphtho[1,2-d]thiazol-2-ylcabamoyl]phenyl}-2-methylacrylic acid (A401)

1H-NMR(DMSO-d6) 12.91(bs, 1H), 7.96(s, 1H), 7.93(s, 1H), 7.65(d, 1H, J=7.6 Hz), 7.33(s, 1H), 7.21(t, 1H, J=7.6 Hz), 7.09(d, 1H, J=7.6 Hz), 3.36(t, 2H, J=6.4 Hz), 3.28(t, 2H, J=7.0 Hz), 2.95-2.99(m, 4H), 2.74(t, 2H, J=7.0 Hz), 1.78(s, 3H), 1.69-1.75(m, 2H), 1.48-1.55(m, 2H), 1.22-1.34(m, 4H), 0.90-0.94(m, 3H).

Example 21
Synthesis of (Z)-3-{2,6-difluoro-4-[6-(3-methyloxyhexyl)-4,5-dihydronaphtho[1,2-d]thiazol-2-ylcabamoyl]phenyl}-2-methyloxyacrylic acid (A423)

1H-NMR(DMSO-d6) 12.92(bs, 1H), 7.91(s, 1H), 7.89(s, 1H), 7.65(d, 1H, J=7.6 Hz), 7.20(t, 1H, J=7.6 Hz), 7.09(d, 1H, J=7.6 Hz), 6.65(s, 1H), 3.7 (s, 3H), 3.22(s, 3H), 3.14-3.22(m, 1H), 2.95-2.99(m, 4H), 2.55-2.70(m, 2H), 1.60-1.69(m, 2H), 1.45-1.55(m, 2H), 1.22-1.34(m, 2H), 0.90-094(m, 3H).

Example 22
Synthesis of (Z)-3-{4-[6-(3-ethyloxypropyl)-4,5-dihydronaphtho[1,2-d]thiazol-2-ylcabamoyl]-2,6-difluorophenyl}-2-methyloxyacrylic acid (A430)

1H-NMR(DMSO-d6) 12.92(bs, 1H), 7.91(s, 1H), 7.89(s, 1H), 7.64(d, 1H, J=7.6 Hz), 7.21(t, 1H, J=7.6 Hz), 7.06(d, 1H, J=7.6 Hz), 6.61(s, 1H), 3.71(s, 3H), 3.33-3.40(m, 4H), 2.95-2.99(m, 4H), 2.71(t, 2H, J=7.0 Hz), 1.70-1.80(m, 2H), 1.13(t, 3H, J=7.0 Hz).

Example 23
Synthesis of (Z)-3-{2,6-difluoro-4-[6-(3-propyloxypropyl)-4,5-dihydronaphtho[1,2-d]thiazol-2-ylcabamoyl]phenyl}-2-methyloxyacrylic acid (A440)

1H-NMR(DMSO-d6) 12.92(bs, 1H), 7.92(s, 1H), 7.89(s, 1H), 7.64(d, 1H, J=7.6 Hz), 7.21(t, 1H, J=7.6 Hz), 7.06(d, 1H, J=7.6 Hz), 6.62(s, 1H), 3.71(s, 3H), 3.33-3.40(m, 4H), 2.95-2.99(m, 4H), 2.71(t, 2H, J=7.0 Hz), 1.70-1.80(m, 2H), 1.45-1.55(m, 2H), 0.89 (t, 3H, J=7.0 Hz).

Example 24
Synthesis of (Z)-3-{2,6-difluoro-4-[6-(3-isopropyloxypropyl)-4,5-dihydronaphtho[1,2-d]thiazol-2-ylcabamoyl]phenyl}-2-methyloxyacrylic acid (A450)

1H-NMR(DMSO-d6) 12.92(bs, 1H), 7.91(s, 1H), 7.89(s, 1H), 7.64(d, 1H, J=7.6 Hz), 7.20(t, 1H, J=7.6 Hz), 7.04(d, 1H, J=7.6 Hz), 6.66(s, 1H), 3.71(s, 3H), 3.50-3.60(m, 1H), 3.38(t, 2H, J=7.0 Hz), 2.95-2.99(m, 4H), 2.69(t, 2H, J=7.0 Hz), 1.70-1.80(m, 2H), 1.11(d, 6H, J=6.0 Hz).

Example 25
Synthesis of (Z)-3-(4-{6-[3-(2,2-dimethylpropyloxy)propyl]-4,5-dihydronaphtho[1,2-d]thiazol-2-ylcabamoyl]-2,6-difluorophenyl}-2-methyloxyacrylic acid (A500)

1H-NMR(DMSO-d6) 12.92(bs, 1H), 7.90(s, 1H), 7.88(s, 1H), 7.64(d, 1H, J=7.6 Hz), 7.20(t, 1H, J=7.6 Hz), 7.04(d, 1H, J=7.6 Hz), 6.65(s, 1H), 3.71(s, 3H), 3.40(t, 2H, J=7.0 Hz), 3.07(s, 2H), 2.95-2.99(m, 4H), 2.69(t, 2H, J=7.0 Hz), 1.70-1.80(m, 2H), 0.90(s, 9H).

Example 26
Synthesis of (E)-3-{2,6-dichloro-4-[6-(3,3-dimethylbutyl)-4,5-dihydronaphtho[1,2-d]thiazol-2-ylcabamoyl]phenyl}-2-methylacrylic acid (A601)

1H-NMR(DMSO-d6) 12.99(bs, 2H), 8.28(s, 2H), 7.61-7.64(m, 1H), 7.40(d, 1H, J=1.3 Hz), 7.18-7.23(m, 1H), 7.07-7.10(m, 1H), 2.98(s, 4H), 2.49-2.64(m, 2H), 1.69(s, 3H), 1.35-1.41(m, 2H), 0.98(s, 9H).

Example 27
Synthesis of (E)-3-{2,6-dichloro-4-[6-(3-methyloxypentyl)-4,5-dihydronaphtho[1,2-d]thiazol-2-ylcabamoyl]phenyl}-2-methylacrylic acid (A928)

1H-NMR(DMSO-d6) 12.95(bs, 1H), 8.28(s, 2H), 7.64(d, 1H, J=7.6 Hz), 7.40(s, 1H), 7.21(t, 1H, J=7.6 Hz), 7.09(d, 1H, J=7.6 Hz), 3.27(s, 3H), 3.10-3.16(m, 1H), 2.95-2.99(m, 4H), 2.65-2.80(m, 2H), 1.68(s, 3H), 1.60-1.69(m, 2H), 1.45-1.55(m, 2H), 0.86(t, 3H, J=7.6 Hz).

Example 28
Synthesis of (E)-3-{2,6-dichloro-4-[6-(3-methyloxyheptyl)-4,5-dihydronaphtho[1,2-d]thiazol-2-ylcabamoyl]phenyl}-2-methylacrylic acid (A930)

1H-NMR(DMSO-d6) 12.95(bs, 1H), 8.28(s, 2H), 7.64(d, 1H, J=7.6 Hz), 7.40(s, 1H), 7.21(t, 1H, J=7.6 Hz), 7.09(d, 1H, J=7.6Hz), 3.27(s, 3H), 3.14-3.22(m, 1H), 2.95-2.99(m, 4H), 2.55-2.65(m, 2H), 1.68(s, 3H), 1.66-1.69(m, 2H), 1.45-1.55(m, 2H), 1.22-1.34(m, 4H), 0.90-094(m, 3H).

Example 29
Synthesis of (E)-3-{2,6-dichloro-4-[6-(3-methyloxy-4,4-dimethylpentyl)-4,5-dihydronaphtho[1,2-d]thiazol-2-ylcabamoyl]phenyl}-2-methylacrylic acid (A932)

1H-NMR(DMSO-d6) 12.95(bs, 1H), 8.28(s, 2H), 7.64(d, 1H, J=7.6 Hz), 7.40(d, 1H), J=1.3 Hz), 7.21(t, 1H, J=7.6 Hz), 7.09(d, 1H, J=7.6 Hz), 3.44(s, 3H), 2.95-2.99(m, 4H), 2.65-2.70(m, 2H), 1.68(s, 3H), 1.45-1.55(m, 2H), 0.90(s, 9H).

Example 30
Synthesis of (E)-3-{2,6-dichloro-4-[6-(3-ethyloxypentyl)-4,5-dihydronaphtho[1,2-d]thiazol-2-ylcabamoyl]phenyl}-2-methylacrylic acid (A936)

1H-NMR(DMSO-d6) 12.95(bs, 1H), 8.28(s, 2H), 7.64(d, 1H, J=7.6 Hz), 7.40(s, 1H), 7.21(t, 1H, J=7.6 Hz), 7.09(d, 1H, J=7.6 Hz), 3.45(q, 2H, J=7.0 Hz), 3.20-3.26(m, 1H), 2.95-2.99(m, 4H), 2.65-2.80(m, 2H), 1.68(s, 3H), 1.60-1.69(m, 2H), 1.45-1.55(m, 2H), 1.13 (t, 3H, J=7.0 Hz), 0.86(t, 3H, J=7.6 Hz).

Example 31
Synthesis of (E)-3-{2,6-dichloro-4-[6-(3-ethyloxyhexyl)-4,5-dihydronaphtho[1,2-d]thiazol-2-ylcabamoyl]phenyl}-2-methylacrylic acid (A937)

1H-NMR(DMSO-d6) 12.95(bs, 1H), 8.28(s, 2H), 7.63(d, 1H, J=7.6 Hz), 7.40(s, 1H), 7.21(t, 1H, J=7.6 Hz), 7.07(d, 1H,J=7.6 Hz), 3.47(q, 2H, J=7.0 Hz), 3.20-3.26(m, 1H), 2.95-2.99(m, 4H), 2.65-2.80(m, 2H), 1.68(s, 3H), 1.60-1.69(m, 2H), 1.45-1.55(m, 2H), 1.30-1.40(m, 2H), 1.13(t, 3H, J=7.0 Hz), 0.86(t, 3H, J=7.6 Hz),

Example 32
Synthesis of (E)-3-{2,6-dichloro-4-[6-(3-ethyloxyheptyl)-4,5-dihydronaphtho[1,2-d]thiazol-2-ylcabamoyl]phenyl}-2-methylacrylic acid (A939)

1H-NMR(DMSO-d6) 12.95(bs, 1H), 8.23(s, 2H), 7.63(d, 1H, J=7.6 Hz), 7.40(s, 1H), 7.21(t, 1H, J=7.6 Hz), 7.10(d, 1H, J=7.6 Hz), 3.47(q, 2H, J=7.0 Hz), 3.20-3.26(m, 1H), 2.95-2.99(m, 4H), 2.65-2.80(m, 2H), 1.68(s, 3H), 1.60-1.69)m, 2H), 1.45-1.55(m, 2H), 1.30-1.40(m, 4H), 1.13(t, 3H, J=7.0 Hz), 0.86-0.89(m, 3H).

Example 33
Synthesis of (E)-3-{2,6-dichloro-4-[6-(3-ethyloxy-4,4-dimethylpentyl)-4,5-dihydronaphtho[1,2-d]thiazol-2-ylcabamoyl]phenyl}-2-methylacrylic acid (A941)

1H-NMR(DMSO-d6) 12.95(bs, 1H), 8.28(s, 2H), 7.64(d, 1H, J=7.6 Hz), 7.40(s, 1H), 7.21(t, 1H, J=7.6 Hz), 7.12(d, 1H, J=7.6 Hz), 3.50-3.65(m, 2H), 2.95-2.99(m, 4H), 2.80-2.90(m, 2H), 2.59-2.65(m, 1H), 1.68(s, 3H), 1.60-1.70(m, 1H), 1.45-1.50(m, 1H), 1.17(t, 3H, J=7.0 Hz), 0.90(s, 9H).

Example 34
Synthesis of (E)-3-{2,6-dichloro-4-[6-(3-propyloxypropyl)-4,5-dihydronaphtho[1,2-d]thiazol-2-ylcabamoyl]phenyl}-2-methylacrylic acid (A944)

1H-NMR(DMSO-d6) 12.92(bs, 1H), 8.28(s, 2H), 7.64(d, 1H, J=7.6 Hz), 7.40(d, 1H, J=1.3 Hz), 7.2(t, 1H, J=7.6 Hz), 7.09(d, 1H, J=7.6 Hz), 3.33-3.40(m, 4H), 2.95-2.99(m, 4H), 2.70(t, 2H, J=7.0 Hz), 1.70-1.80(m, 2H), 1.66(s, 3H), 1.45-1.53(m, 2H), 0.88(t, 3H, J=7.4 Hz).

Example 35
Synthesis of (E)-3-{2,6-dichloro-4-[6-(3-isopropyloxypropyl)-4,5-dihydronaphtho[1,2-d]thiazol-2-ylcabamoyl]phenyl}-2-methylacrylic acid (A954)

1H-NMR(DMSO-d6) 12.9(bs, 1H), 8.28(s, 2H), 7.64(d, 1H, J=7.6 Hz), 7.40(d, 1H, J=1.3 Hz), 7.21(t, 1H, J=7.6 Hz), 7.09(d, 1H, J=7.6 Hz), 3.50-3.58(m, 1H), 3.38(t, 2H, J=7.0), 2.95-2.99(m, 4H), 2.70(t, 2H, J=7.0 Hz), 1.70-1.80(m, 2H). 1.66(s, 3H), 1.10(d, 6H, J=6.0 Hz).

Example 36
Synthesis of (E)-3-{2,6-dichloro-4-[6-(3-pentyloxypropyl)-4,5-dihydronaphtho[1,2-d]thiazol-2-ylcabamoyl]phenyl}-2-methylacrylic acid (A993)

1H-NMR(DMSO-d6) 12.95(bs, 1H), 8.24(s, 2H), 7.64(d, 1H, J=7.6 Hz), 7.40(s, 1H), 7.21 (t, 1H, J=7.6 Hz), 7.09(d, 1H, J=7.6 Hz), 3.36(t, 2H, J=6.4 Hz), 3.28(t, 2H, J=7.0 Hz), 2.95-2.99(m, 4H), 2.70(t, 2H, J=7.0 Hz), 1.69-1.75(m, 2H), 1.68(s, 3H), 1.48-1.55(m, 2H), 1.22-1.34(m, 4H), 0.90-0.94(m, 3H).

Example 37
Synthesis of (E)-3-(2,6-dichloro-4-{6-[3-(2,2-dimethylpropyloxy)propyl]-4,5-dihydronaphtho[1,2-d]thiazol-2-ylcabamoyl]phenyl}-2-methylacrylic acid (A1003)

1H-NMR(DMSO-d6) 12.95(bs, 1H), 8.27(s, 2H), 7.64(d, 1H, J=7.6 Hz), 7.40(d, 1H, J=1.3 Hz), 7.21(t, 1H, J=7.6 Hz), 7.09(d, 1H, J=7.6 Hz), 3.38(t, 2H, J=7.0 Hz), 3.07(s, 2H), 2.95-2.99(m, 4H), 2.70(t, 2H, J=7.0 Hz), 1.70-1.80(m, 2H), 1.68(s, 3H), 0.90(s, 9H).

Example 38
Synthesis of (Z)-3-{2,6-dichloro-4-[6-(3-methyloxyhexyl)-4,5-dihydronaphtho[1,2-d]thiazol-2-ylcabamoyl]phenyl}-2-methyloxyacrylic acid (A1016)

1H-NMR(DMSO-d6) 12.92(bs, 1H), 8.23(s, 2H), 7.64(d, 1H, J=7.6 Hz), 7.21(t, 1H, J=7.6 Hz), 7.09(d, 1H, J=7.6 Hz), 6.76(s, 1H), 3.60(s, 3H), 3.27(s, 3H), 3.14-3.22(m, 1H), 2.95-2.99(m, 4H), 2.55-2.75(m, 2H), 1.60-1.69(m, 2H), 1.45-1.55(m, 2H), 1.22-1.34(m, 2H), 0.90-094(m, 3H).

Example 39
Synthesis of (Z)-3-{2,6-dichloro-4-[6-(3-methyloxyheptyl)-4,5-dihydronaphtho[1,2-d]thiazol-2-ylcabamoyl]phenyl}-2-methyloxyacrylic acid (A1018)

1H-NMR(DMSO-d6) 12.95(bs, 1H), 8.27(s, 2H), 7.64(d, 1H, J=7.6 Hz ), 7.21(t, 1H, J=7.6 Hz), 7.09(d, 1H, J=7.6 Hz ), 6.73(s, 1H), 3.61(s, 3H), 3.27(s, 3H), 3.14-3.22(m, 1H), 2.95-2.99(m, 4H), 2.55-2.65(m, 2H), 1.62-1.69(m, 2H), 1.45-1.55(m, 2H), 1.22-1.34(m, 2H), 0.90-094(m, 3H).

Example 40
Synthesis of (Z)-3-{2,6-dichloro-4-[6-(3-propyloxypropyl)-4,5-dihydronaphtho[1,2-d]thiazol-2-ylcabamoyl]phenyl}-2-methyloxyacrylic acid (A1033)

1H-NMR(DMSO-d6) 12.95(bs, 1H), 8.23(s, 2H), 7.62(d, 1H, J=7.6 Hz), 7.21(t, 1H, J=7.6 Hz), 7.09(d, 1H, J=7.6 Hz), 6.73(s, 1H), 3.61(s, 3H), 3.33-3.40(m, 4H), 2.95-2.99(m, 4H,, 2.70(t, 2H, J=7.0 Hz), 1.70-1.80(m, 2H), 1.45-1.53 (m, 2H), 0.89(t, 3H, J=7.0 Hz).

Example 41
Synthesis of (E)-3-{2,6-dichloro-4-[6-(3-propyloxypropyl)-4H-chromeno[4,3-d]thiazol-2-ylcabamoyl]phenyl}-2-methylacrylic acid (A1123)

1H-NMR(DMSO-d6) 12.9 (bs, 1H), 8.28(s, 2H), 7.49(d, 1H, J=7.6 Hz), 7.38(s, 1H), 7.09(d, 1H, J=7.6 Hz), 6.97(t, 1H, J=7.6 Hz), 5.49(s, 2H), 3.33-3.40(m, 4H), 2.63(t, 2H, J=7.0 Hz), 1.70-1.80(m, 2H), 1.68(s, 3H), 1.45-1.53(m, 2H), 0.89(t, 3H), J=7.4 Hz).

Example 42
Synthesis of (E)-3-{2,6-difluoro-4-[6-(3-methyloxy-3-methylbutyl)-4,5-dihydronaphto[1,2-d]thiazol-2-ylcabamoyl]phenyl}-2-methylacrylic acid (A1295)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 7.96(s, 1H), 7.93(s, 1H), 7.65(d, 1H, J=7.5 Hz), 7.33(s, 1H), 7.21(t, 2H, J=7.5 Hz), 7.11(d, 1H, J=7.5 Hz), 3.18(s, 3H), 2.60-2.65(m, 2H), 1.79(s, 3H), 1.60-1.69(m, 2H), 1.18(s, 6H).

Example 43
Synthesis of (E)-3-(4-{6-[3-(2-ethyloxy-1-ethyloxymethylethyloxy)propyl]-4,5-dihydronaphtho[1,2-d]thiazol-2-ylcabamoyl]-2,6-difluorophenyl}-2-methylacrylic acid (A1296)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 7.97(s, 1H), 7.94(s, 1H), 7.65(d, 1H, J=7.5 Hz), 7.33(s, 1H), 7.21(t, 2H, J=7.5 Hz), 7.10(d, 1H, J=7.5 Hz), 3.56-3.60(m, 4H), 3.40-3.50(m, 7H), 2.95-2.99 (m, 4H), 2.69(t, 2H, J=7.3 Hz), 1.79(s, 3H), 1.67-1.73(m, 2H), 1.10(t, 6H, J=7.3 Hz).

Example 44
Synthesis of (E)-3-(2,6-difluoro-4-{6-[3-(2-isopropyloxyethyloxy)propyl]-4,5-dihydronaphtho[1,2-d]thiazol-2-ylcabamoyl}phenyl)-2-methylacrylic acid (A1297)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 7.97(s, 1H), 7.94(s, 1H), 7.65(d, 1H, J=7.5 Hz), 7.33(s, 1H), 7.21(t, 2H, J=7.5 Hz), 7.11(d, 1H, J=7.5 Hz), 3.56-3.60(m, 2H), 2.95-2.99 (m, 4H), 2.70 (t, 2H, J=7.4 Hz), 1.78 (s, 3H), 1.65-1.70 (m, 2H), 1.10 (d, 6H, J=6.0 Hz),

Example 45
Synthesis of (E)-3-(2,6-difluoro-4-{6-[3-(2-ethyloxy-1-ethyloxymethylethyloxy)propyl]-4,5-dihydronaphtho[1,2-d]thiazol-2-ylcabamoyl}phenyl)-2-methylacrylic acid (A1298)

1H-NMR(DMSO-d6) 12.97(bs, 1H), 8.27(s, 2H), 7.66(d, 1H, J=7.6 Hz), 7.39(s, 1H), 7.20(t, 1H, J=7.6 Hz), 7.09(d, 1H, J=7.6 Hz), 3.56-3.60(m, 4H), 3.40-3.50(m, 7H), 2.95-2.99(m, 4H), 2.69(t, 2H, J=7.2 Hz), 1.65-1.78(m, 2H), 1.69(s, 3H), 1.02(t, 6H, J=7.2 Hz).

Example 46
Synthesis of (E)-3-(2,6-dichloro-4-{6-[3-(2-methyloxyethyloxy)propyl]-4,5-dihydronaphtho[1,2-d]thiazol-2-ylcabamoyl}phenyl)-2-methylacrylic acid (A1299)

1H-NMR(DMSO-d6) 12.92(bs, 1H,), 8.28(s, 2H,), 7.64(d, 1H, J=7.6 Hz), 7.40(d, 1H, J=1.3 Hz), 7.21(t, 1H, J=7.6 Hz), 7.09(d, 1H, J=7.6 Hz), 3.40-3.50(m, 6H), 3.18(s, 3H), 2.95-2.99(m, 4H), 2.68(t, 2H, J=7.4 Hz), 1.68-1.78(m, 2H), 1.68(s, 3H).

Example 47
Synthesis of (E)-3-(2,6-difluoro-4-{6-[3-(2-methyloxyethyloxy)propyl]-4,5dihydronaphtho[1,2-d]thiazol-2-ylcabamoyl}phenyl)-2-methylacrylic acid (A1300)

1H-NMR(DMSO-d6) 12.91(bs, 1H), 7.96(s, 1H), 7.93(s, 1H), 7.65(d, 1H, J=7.6 Hz), 7.33 (d, 1H, J=1.3 Hz), 7.21(t, 1H, J=7.6 Hz), 7.09(d, 1H, J=7.6 Hz), 3.40-3.50(m, 6H), 3.18(s, 3H), 2.95-2.99(m, 4H), 2.68(t, 2H, J=7.4 Hz), 1.80-1.88(m, 2H), 1.78(s, 3H),

Example 48
Synthesis of (E)-3-[2,6-difluoro-4-(6-hexyloxy-4,5-dihydronaphtho[1,2-d]thiazol-2-ylcabamoyl)phenyl]-2-methylacrylic acid (A1301)

1H-NMR(DMSO-d6) 12.91(bs, 1H), 7.96(s, 1H), 7.94(s, 1H), 7.37(d, 1H, J=7.6 Hz), 7.33(s, 1H), 7.24(t, 1H, J=7.6 Hz), 6.92(d, 1H, J=7.6 Hz), 4.00(t, 2H, J=7.0 Hz), 2.95-2.99(m, 4H), 1.80(s, 3H), 1.70-1.80(m, 2H), 1.45-1.55(m, 2H), 1.30-1.40(m, 4H), 0.89-0.91(m, 3H).

Example 49
Synthesis of (E)-3-[2,6-dichloro-4-(6-hexyloxy-4,5-dihydronaphtho[1,2-d]thiazol-2-ylcabamoyl)phenyl]-2-methylacrylic acid (A1302)

1H-NMR(DMSO-d6) 12.92(bs, 1H), 8.28(s, 2H), 7.39(s, 1H), 7.37(d, 1H, J=7.6 Hz), 7.24(t, 1H, J=7.6 Hz), 6.91(d, 1H, J=7.6 Hz), 4.00(t, 2H, J=7.0 Hz), 2.95-2.99(m, 4H), 1.70-1.80(m, 2H), 1.68(s, 3H), 1.45-1.55(m, 2H), 1.30-1.40(m, 4H), 0.89-0.91(m, 3H).

Example 50
Synthesis of (E)-3-[2,6-dichloro-4-(6-isobutyloxy-4,5-dihydronaphtho[1,2-d]thiazol-2-ylcabamoyl)phenyl]-2-methylacrylic acid (A1303)

1H-NMR(DMSO-d6) 12.92(bs, 1H), 8.28(s, 2H), 7.39(s, 1H), 7.37(d, 1H, J=7.6 Hz), 7.24(t, 1H, J=7.6 Hz), 6.89(d, 1H, J=7.6 Hz), 3.79(d, 2H, J=6.6 Hz), 2.95-2.99(m, 4H), 2.05-2.15(m, 1H), 1.68(s, 3H), 1.02(d, 6H, J=6.0 Hz).

Example 51
Synthesis of (E)-3-[2,6-difluoro-4-(6-isobutyloxy-4,5-dihydronaphtho[1,2-d]thiazol-2-ylcabamoyl)phenyl]-2-methylacrylic acid (A1304)

1H-NMR(DMSO-d6) 12.93(bs, 1H), 7.96(s, 1H), 7.94(s, 1H), 7.37(d, 1H, J=7.6 Hz), 7.33(s, 1H), 7.24(t, 1H, J=7.6 Hz), 6.92(d, 1H, J=7.6.Hz), 3.79(d, 2H, J=6.6 Hz), 2.95-2.99(m, 4H), 2.05-2.15(m, 1H), 1.78(s, 3H), 1.02(d, 6H, J=6.0 Hz).

Example 52
Synthesis of (E)-3-{4-[6-(2-ethyloxyethyloxy)-4,5-dihydronaphtho[1,2-d]thiazol-2-ylcabamoyl]-2,6-difluorophenyl}-2-methylacrylic acid (A1305)

1H-NMR(DMSO-d6) 12.93(bs, 1H), 7.96(s, 1H), 7.94(s, 1H), 7.40(d, 1H, J=7.6 Hz), 7.33(s, 1H), 7.24(t, 1H, J=7.6 Hz), 6.95(d, 1H, J=7.6 Hz ), 4.13(t, 2H, J=5.0 Hz), 3.73(t, 2H, J=5.0 Hz), 3.54(q, 2H, J=7.0 Hz), 2.95-2.99(m, 4H,), 1.78(s, 3H), 1.15(t, 3H, J=7.0 Hz).

Example 53
Synthesis of (E)-3-{2,6-dichloro-4-[6-(2-ethyloxyethyloxy)-4,5-dihydronaphtho[1,2-d]thiazol-2-ylcabamoyl]phenyl}-2-methylacrylic acid (A1306)

1H-NMR(DMSO-d6) 12.92(bs, 1H), 8.28(s, 2H), 7.39(s, 1H), 7.37(d, 1H, J=7.6 Hz), 7.24(t, 1H, J=7.6 Hz), 6.95(d, 1H, J=7.6 Hz ), 4.13(t, 2H, J=5.0 Hz), 3.73(t, 2H, J=5.0 Hz), 3.54(q, 2H, J=7.0 Hz), 2.95-2.99(m, 4H), 1.68(s, 3H), 1.14(t, 3H, J=7.0 Hz).

Example 54
Synthesis of (E)-3-[4-(6-ethyl-4H-chromeno[4,3-d]thiazol-2-ylcabamoyl]-2,6-difluorophenyl}-2-methylacrylic acid (A1307)

1H-NMR(DMSO-d6) 12.93(bs, 1H), 7.96(s, 1H), 7.94(s, 1H), 7.48(d, 1H, J=7.6 Hz), 7.33(s, 1H), 7.11 d, 1H, J=7.6 Hz), 6.97(d, 1H, J=7.6 Hz), 5.49(s, 2H), 2.60(q, 2H, J=7.0 Hz), 1.79(s, 3H), 1.14(t, 3H, J=7.0 Hz).

Example 55
Synthesis of (E)-3-[2,6-difluoro-4-(6-propyl-4H-chromeno[4,3-d]thiazol-2-ylcabamoyl)phenyl]-2-methylacrylic acid (A1308)

1H-NMR(DMSO-d6) 12.93(bs, 1H), 7.96(s, 1H), 7.94(s, 1H), 7.49(d, 1H, J=7.6 Hz), 7.33(s, 1H), 7.07(d, 1H, J=7.6 Hz), 6.97(t, 1H, J=7.6 Hz ), 5.47(s, 2H), 2.53(t, 2H, J=7.0 Hz), 1.79(s, 3H), 1.49-1.59(m, 2H), 0.94(t, 3H, J=7.0 Hz).

Example 56
Synthesis of (E)-3-[2,6-dichloro-4-(6-ethyl-4H-chromeno[4,3-d]thiazol-2-ylcabamoyl)phenyl]-2-methylacrylic acid (A1310)

1H-NMR(DMSO-d6) 12.92(bs, 1H), 8.26(s, 2H), 7.47(d, 1H, J=7.6 Hz), 7.38(s, 1H), 7.09(d 1H, J=7.6 Hz), 6.95(t, 1H, J=7.6 Hz), 5.49(s, 2H), 2.55(q, 2H), J=7.0 Hz), 1.69(s, 3H), 1.14 t, 3H, J=7.0 Hz).

Example 57
Synthesis of (E)-3-[2,6-dichloro-4-(6-propyl-4H-chromeno[4,3-d]thiazol-2-ylcabamoyl)phenyl]-2-methylacrylic acid (A1311)

1H-NMR(DMSO-d6) 12.92(bs, 1H), 8.27(s, 2H), 7.47(d, 1H, J=7.6 Hz), 7.38(s, 1H), 7.09(d, 1H, J=7.6 Hz), 6.95(t, 1H, J=7.6 Hz), 5.49(s, 2H), 2.53(t, 2H, J=7.0 Hz), 1.66(s, 3H), 1.49-1.59(m, 2H), 0.94(t, 3H, J=7.0 Hz).

Example 58
Synthesis of (E)-3-[2,6-dichloro-4-(6-isopropyl-4H-chromeno[4,3-d]thiazol-2-ylcabamoyl)phenyl]-2-methylacrylic acid (A1312)

1H-NMR(DMSO-d6) 12.92(bs, 1H), 8.27(s, 2H), 7.49(d, 1H, J=7.6 Hz), 7.38(s, 1H), 7.13(d, 1H, J=7.6 Hz), 7.01(t, 1H, J=7.6 Hz), 5.49(s, 2H), 3.20-3.30(m, 2H), 1.69(s, 3H), 1.04(d, 6H, J=6.0 Hz).

Example 59
Synthesis of (E)-3-{2,6-difluoro-4-[6-(3-propyloxypropyl)-4H-chromeno[4,3-d]thiazol-2-ylcabamoyl]phenyl}-2-methylacrylic acid (A1313)

1H-NMR(DMSO-d6) 12.93(bs, 1H), 7.96(s, 1H), 7.94(s, 1H), 7.49(d, 1H, J=7.6 Hz), 7.33(s, 1H), 7.10(d, 1H, J=7.6 Hz), 6.95(t, 1H, J=7.6 Hz), 5.49(s, 2H), 3.33-3.40(m, 4H), 2.63(t, 2H, J=7.0 Hz), 1.80(s, 3H), 1.70-1.80(m, 2H), 1.45-1.53(m, 2H), 0.89(t, 3H, J=7.4 Hz).

Example 60
Synthesis of (E)-3-[2,6-difluoro-4-(6-hexyl-4H-chromeno[4,3-d]thiazol-2-ylcabamoyl)phenyl]-2-methylacrylic acid (A1314)

1H-NMR(DMSO-d6) 12.93(bs, 1H), 7.96(s, 1H), 7.94(s, 1H), 7.49(d, 1H, J=7.6 Hz), 7.33(s, 1H), 7.10(d, 1H, J=7.6 Hz), 6.97(t, 1H, J=7.6 Hz), 5.47(s, 2H), 2.53(t, 2H, J=7.0 Hz), 1.80(s, 3H), 1.49-1.59(m, 2H), 1.25-1.36(m, 6H), 0.94(t, 3H, J=7.0 Hz).

Example 61
Synthesis of (E)-3-{4-[6-(3,3-dimethylbutyl)-4H-chromeno[4,3-d]thiazol-2-ylcabamoyl]-2,6-difluorophenyl}-2-methylacrylic acid (A1315)

1H-NMR(DMSO-d6) 12.93(bs, 1H), 7.96(s, 1H), 7.94(s, 1H), 7.4 (d, 1H, J=7.6 Hz), 7.33(s, 1H), 7.10(d, 1H, J=7.6 Hz), 6.97(t, 1H, J=7.6 Hz), 5.47(s, 2H), 2.50-2.60(m, 2H), 1.80(s, 3H), 1.39-1.45(m, 2H), 0.95(s, 9H).

Example 62
Synthesis of (E)-3-[2,6-dichloro-4-(6-hexyl-4H-chromeno[4,3-d]thiazol-2-ylcabamoyl)phenyl]-2-methylacrylic acid (A1316)

1H-NMR(DMSO-d6) 12.92(bs, 1H), 8.27(s, 2H), 7.48(d, 1H, J=7.6 Hz), 7.3 (s, 1H), 7.09(d, 1H, J=7.6 Hz), 6.97(t, 1H, J=7.6 Hz), 5.49(s, 2H), 2.56(t, 2H, J=7.0 Hz), 1.68(s, 3H), 1.49-1.59(m, 2H), 1.25-1.36(m, 6H), 0.86(t, 3H, J=7.0 Hz).

Example 63
Synthesis of (E)-3-{2,6-dichloro-4-[6-(3,3-dimethylbutyl)-4H-chromeno[4,3-d]thiazol-2-ylcabamoyl]phenyl}-2-methylacrylic acid (A1317)

1H-NMR(DMSO-d6) 12.92(bs, 1H), 8.28(s, 2H), 7.50(d, 1H, J=7.6 Hz), 7.40(s, 1H), 7.09(d, 1H, J=7.6 Hz), 6.96(t, 1H, J=7.6 Hz), 5.49(s, 2H), 2.50-2.60(m, 2H), 1.68(s, 3H), 1.39-1.45(m, 2H), 0.95(s, 9H).

Example 64
Synthesis of (Z)-3-{2,6-dichloro-4-[6-(3,3-dimethylbutyl)-4,5-dihydronaphtho[1,2-d]thiazol-2-ylcabamoyl]phenyl}-2-methyloxyacrylic acid (A1318)

1H-NMR(DMSO-d6) 12.90 (bs, 2H), 8.23 (s, 2H), 7.63 (d, 1H, J=7.5 Hz), 7.20 (t, 1H, J=7.5 Hz), 7.08 (d, 1H, J=7.7 Hz), 6.73 (s, 1H), 3.61 (s, 3H), 2.98 (s, 4H), 2.49-2.64 (m, 2H), 1.35-1.41 (m, 2H), 0.98 (s, 9H).

Example 65
Synthesis of (Z)-3-{4-[6-(3,3-dimethylbutyl)-4,5-dihydronaphtho[1,2-d]thiazol-2-ylcabamoyl]-2,6-difluorophenyl}-2-methyloxyacrylic acid (A1319)

1H-NMR(DMSO-d6) 12.87 (bs, 2H), 7.88-7.91 (m, 2H), 7.62-7.65 (m, 1H), 7.20 (t, 1H, J=7.5 Hz), 7.07-7.09 (m, 1H), 6.65 (s, 1H), 3.71 (s, 3H), 2.98 (s, 4H), 2.49-2.64 (m, 2H), 1.35-1.41 (m, 2H), 0.98 (s, 9H).

Example 66
Synthesis of (E)-3-[2,6-difluoro-4-(5-pentyl-4,5-dihydronaphtho[1,2-d]thiazol-2-ylcabamoyl)phenyl]-2-methylacrylic acid (A1320)

1H-NMR(DMSO-d6) 12.91(bs, 1H), 7.96(s, 1H), 7.93(s, 1H), 7.73(d, 1H, J=7.6 Hz), 7.39(s, 1H), 7.22-7.35(m, 3H), 2.94-3.16(m, 3H), 1.80(s, 3H), 1.40-1.55(m, 2H), 1.20-1.30(m, 6H), 0.86 (t, 3H, J=7.0 Hz).

Example 67
Synthesis of (E)-3-[2,6-dichloro-4-(5-pentyl-4,5-dihydronaphtho[1,2-d]thiazol-2-ylcabamoyl)phenyl]-2-methylacrylic acid (A1321)

1H-NMR(DMSO-d6) 12.91(bs, 1H), 8.28(s, 2H), 7.73(d, 1H, J=7.6 Hz), 7.39(s, 1H), 7.22-7.35(m, 3H), 2.94-3.16(m, 3H), 1.69(s, 3H), 1.40-1.55(m, 2H), 1.20-1.30(m, 6H), 0.86 (t, 3H, J=7.0 Hz).

Example 68
Synthesis of (E)-3-[2,6-difluoro-4-(5-heptyl-4,5-dihydronaphtho[1,2-d]thiazol-2-ylcabamoyl)phenyl]-2-methylacrylic acid (A1322)

Example 69
Synthesis of (E)-3-[2,6-difluoro-4-(5-pent-1-ynyl-4,5-dihydronaphtho[1,2-d]thiazol-2-ylcabamoyl)phenyl]-2-methylacrylic acid (A1323)

1H-NMR(DMSO-d6) 12.97(bs, 2H), 7.91-7.99(m, 2H), 7.70-7.73(m, 1H), 7.33(s, 1H), 7.24-7.30(m, 2H), 3.18(t, 2H, J=7.5 Hz), 3.01(t, 2H, J=7.8 Hz), 2.42-2.54(m, 2H), 1.80(s, 3H), 1.55-1.66(m, 2H), 1.04(t, 3H, J=7.5 Hz).

Example 70
Synthesis of (E)-3-[2,6-difluoro-4-(6-hept-1-ynyl-4,5-dihydronaphtho[1,2-d]thiazol-2-ylcabamoyl)phenyl]-2-methylacrylic acid (A1324)

1H-NMR(DMSO-d6) 12.97(bs, 2H), 7.92-8.00(m, 2H), 7.71(t, 1H, J=3.9 Hz), 7.34(s, 1H), 7.28(d, 2H, J=3.6 Hz), 3.17(t, 2H, J=7.8 Hz), 3.01(t, 2H, J=8.1 Hz), 1.81(s, 3H), 1.55-1.64(m, 2H), 1.29-1.49(m, 4H), 0.91(t, 3H, J=7.2 Hz).

Example 71
Synthesis of (E)-3-[4-(6-dec-1-ynyl-4,5-dihydronaphtho[1,2-d]thiazol-2-ylcabamoyl)-2,6-difluorophenyl]-2-methylacrylic acid (A1325)

1H-NMR(DMSO-d6) 12.99(bs, 2H), 7.95(d, 2H, J=7.8 Hz), 7.71(t, 1H, J=4.8 Hz), 7.27-7.34(m, 3H), 3.17(t, 2H, J=8.1 Hz), 3.01(t, 2H, J=8.1 Hz), 1.81(s, 3H), 1.20-1.60(m, 12H), 0.84-0.88(m, 3H).

Example 72
Synthesis of (E)-3-{2,6-difluoro-4-[6-(4-methylpent-1-ynyl-4,5-dihydronaphtho[1,2-d]thiazol-2-ylcabamoyl)phenyl]-2-methylacrylic acid (A1326)

1H-NMR(DMSO-d6) 12.97(bs, 2H), 7.96(d, 2H, J=8.4 Hz), 7.70-7.73(m, 1H), 7.23-7.34(m, 3H), 3.18(t, 2H, J=8.4 Hz), 3.02(t, 2H, J=8.1 Hz), 2.40(d, 2H, J=6.3 Hz), 1.85-1.94(m, 1H), 1.81(s, 3H), 2.07(d, 6H, J=6.6 Hz).

Example 73
Synthesis of (E)-3-[2,6-dichloro-4-(5-heptyl-4,5-dihydronaphtho[1,2-d]thiazol-2-ylcabamoyl)phenyl]-2-methylacrylic acid (A1327)

1H-NMR(DMSO-d6) 12.91(bs, 1H), 8.26(s, 2H), 7.73(d, 1H, J=7.6 Hz), 7.39(s, 1H), 7.22-7.35(m, 3H), 2.94-3.16(m, 3H), 1.69(s, 3H), 1.40-1.55(m, 2H), 1.20-1.30(m, 10H), 0.86(t, 3H, J=7.0 Hz).

Example 74
Synthesis of (E)-3-[4-(5-butyl-4,5-dihydronaphtho[1,2-d]thiazol-2-ylcabamoyl)-2,6-difluorophenyl]-2-methylacrylic acid (A1328)

Example 75
Synthesis of (E)-3-[4-(5-butyl-4,5-dihydronaphtho[1,2-d]thiazol-2-ylcabamoyl)-2,6-dichlorophenyl]-2-methylacrylic acid (A1329)

1H-NMR(DMSO-d6) 12.91(bs, 1H), 8.27(s, 2H), 7.70(d, 1H, J=7.6 Hz), 7.39(s, 1H), 7.22-7.35(m, 3H), 2.94-3.16(m, 3H), 1.69(s, 3H), 1.40-1.55(m, 2H), 1.20-1.30(m, 4H), 0.86 (t, 3H, J=7.0 Hz).

Example 76
Synthesis of (E)-3-[4-(6-cyclohexy-1-enylethynyl-4,5-dihydronaphtho[1,2-d]thiazol-2-ylcabamoyl)-2,6-difluorophenyl]-2-methylacrylic acid (A1330)

1H-NMR(DMSO-d6) 12.97(bs, 2H), 7.92-8.00(m, 2H), 7.72-7.75(m, 1H), 7.29-7.38(m, 3H), 6.20-6.28(m, 1H), 3.17(t, 2H, J=7.5 Hz), 3.02(t, 2H, J=7.5 Hz), 2.06-2.26(m, 4H), 1.81(s, 3H), 1.54-1.70(m, 4H).

Example 77
Synthesis of (E)-3-{2,6-difluoro-4-[6-(3-methyloxyprop-1-ynyl)-4,5-dihydronaphtho[1,2-d]thiazol-2-ylcabamoyl)phenyl]-2-methylacrylic acid (A1331)

1H-NMR(DMSO-d6) 12.98(bs, 2H), 7.92-8.00(m, 2H), 7.75-7.80(m, 1H), 7.29-7.38(m, 3H), 4.40(s, 2H), 3.37(s, 3H), 3.20(t, 2H, J=6.6 Hz), 3.03(t, 2H, J=6.6 Hz), 1.80(s, 3H).

Example 78
Synthesis of (E)-3-{2,6-dichloro-4-[6-(3-ethyloxypentyl)-4,5-dihydronaphtho[1,2-d]thiazol-2-ylcabamoyl)phenyl]-2-methylacrylic acid (A1332)

1H-NMR(CDC13) 7.72(s, 2H), 7.25(s, 2H), 6.99(d, 1H, J=7.6 Hz), 6.94(t, 1H, J=7.6 Hz), 4.27(q, 2H, J=7.0 Hz), 3.49-3.56(m, 2H), 3.20-3.25(m, 1H), 2.95-3.11(m, 4H), 2.60-2.80(m, 2H), 1.60-1.69(m, 2H), 1.61(s, 3H), 1.45-1.55(m, 2H), 1.48 (t, 3H, J=7.0 Hz), 1.28 (t, 3H, J=7.0 Hz), 0.86(t, 3H, J=7.2 Hz).

The compounds described below can be synthesized by similar method described above.
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wherein R⁶, R⁷, and R⁸are independently fluoro, chloro, or methyl;

R^Eis n-pentyl, 3,3-dimethylbuthyl, 1-methyloxyethyl, 1-methyloxypropyl, 1-methyloxybutyl, 1-methyloxy-2-methylpropyl, 1-methyloxypentyl, 1-methyloxy-3-methylbutyl, 1-methyloxy-2,2-dimethylpropyl, 1-methyloxyhexyl, 1-methyloxy-3,3-dimethylbutyl, 1-ethyloxyethyl, 1-ethyloxypropyl, 1-ethyloxybutyl, 1-ethyloxy-2-methylpropyl, 1-ethyloxypentyl, 1-ethyloxy-3-methylbutyl, 1-ethyloxy-2,2-dimethylpropyl, 1-ethyloxyhexyl, 1-ethyloxy-3,3-dimethylbutyl, 1-n-propyloxyethyl, 1-n-propyloxypropyl, 1-n-propyloxybutyl, 1-n-propyloxy-2-methylpropyl, 1-n-propyloxypentyl, 1-n-propyloxy-3-methylbutyl, 1-n-propyloxy-2,2-dimethylpropyl, 1-n-propyloxyhexyl, 1-n-propylloxy-3,3-dimethylbutyl, 1-isopropyloxyethyl, 1-isopropyloxypropyl, 1-isopropyloxybutyl, 1-isopropyloxy-2-methylpropyl, 1-isopropyloxypentyl, 1-isopropyloxy-3-methylbutyl, 1-isopropyloxy-2,2-dimethylpropyl, 1-isopropyloxyhexyl, 1-isopropyloxy-3,3-dimethylbutyl, 1-n-butyloxyethyl, 1-n-butyloxypropyl, 1-n-butyloxybutyl, 1-n-butyloxy-2-methylpropyl, 1-n-butyloxypentyl, 1-n-butyloxy-3-methylbutyl, 1-n-butyloxy-2,2-dimethylpropyl, 1-isobutyloxyhexyl, 1-isobutyloxy-3,3-dimethylbutyl, 1-isobutyloxyethyl, 1-isobutyloxypropyl, 1-isobutyloxybutyl, 1-isobutyloxy-2-methylpropyl, 1-isobutyloxypentyl, 1-isobutyloxy-3-methylbutyl, 1-isobutyloxy-2,2-dimethylpropyl, 1-isobutyloxyhexyl, 1-isobutyloxy-3,3-dimethylbutyl, 1-t-butyloxyethyl, 1-t-butyloxypropyl, 1-t-butyloxybutyl, 1-t-butyloxy-2-methylpropyl, 1-t-butyloxypentyl, 1-t-butyloxy-3-methylbutyl, 1-t-butyloxy-2,2-dimethylpropyl, 1-t-butyloxyhexyl, 1-t-butyloxy-3,3-dimethylbutyl, 1-n-pentyloxyethyl, 1-n-pentyloxypropyl, 1-n-pentyloxybutyl, 1-n-pentyloxy-2-methylpropyl, 1-n-pentylloxypentyl, 1-n-pentyloxy-3-methylbutyl, 1-n-pentyloxy-2,2-dimethylpropyl, 1-n-pentyloxyhexyl, 1-n-pentyloxy-3,3-dimethylbutyl, 1-neopentyloxyethyl, 1-neopentyloxypropyl, 1-neopentyloxybutyl, 1-neopentyloxy-2-methylpropyl, 1-neopentylloxypentyl, 1-neopentyloxy-3-methylbutyl, 1-neopentyloxy-2,2-dimethylpropyl, 1-neopentyloxyhexyl, 1-neopentyloxy-3,3-dimethylbutyl, 3-methyloxypropyl, 3-methyloxybutyl, 3-methyloxypentyl, 3-methyloxyhexyl, 3-methyloxy-4-methylpentyl, 3-methyloxyheptyl, 3-methyloxy-5-methylhexyl, 3-methyloxy-4,4-dimethylpentyl, 3-methyloxyoctyl, 3-methyloxy-5,5-dimethylhexyl, 3-ethyloxypropyl, 3-ethyloxybutyl, 3-ethyloxypentyl, 3-ethyloxyhexyl, 3-ethyloxy-4-methylpentyl, 3-ethyloxyheptyl, 3-ethyloxy-5-methylhexyl, 3-ethyloxy-4,4-dimethylpentyl, 3-ethyloxyoctyl, 3-ethyloxy-5,5-dimethylhexyl, 3-n-propyloxypropyl, 3-n-propyloxybutyl, 3-n-propyloxypentyl, 3-n-propyloxyhexyl, 3-n-propyloxy-4-methylpentyl, 3-n-propyloxyheptyl, 3-n-propyloxy-5-methylhexyl, 3-n-propyloxy-4,4-dimethylpentyl, 3-n-propyloxyoctyl, 3-n-propyloxy-5,5-dimethylhexyl, 3-isopropyloxypropyl, 3-isopropyloxybutyl, 3-isopropyloxypentyl, 3-isopropyloxyhexyl, 3-isopropyloxy-4-methylpentyl, 3-isopropyloxyheptyl, 3-isopropyloxy-5-methylhexyl, 3-isopropyloxy-4,4-dimethylpentyl, 3-isopropyloxyoctyl, 3-isopropyloxy-5,5-dimethylhexyl, 3-n-butyloxypropyl, 3-n-butyloxybutyl, 3-n-butyloxypentyl, 3-n-butyloxyhexyl, 3-n-butyloxy-4-methylpentyl, 3-n-butyloxyheptyl, 3-n-butyloxy-5-methylhexyl, 3-n-butyloxy-4,4-dimethylpentyl, 3-n-butyloxyoctyl, 3-n-butyloxy-5,5-dimethylhexyl, 3-isobutyloxypropyl, 3-isobutyloxybutyl, 3-isobutyloxypentyl, 3-isobutyloxyhexyl, 3-isobutyloxy-4-methylpentyl, 3-isobutyloxyheptyl, 3-isobutyloxy-5-methylhexyl, 3-isobutyloxy-4,4-dimethylpentyl, 3-isobutyloxyoctyl, 3-isobutyloxy-5,5-dimethylhexyl, 3-t-butyloxypropyl, 3-t-butyloxybutyl, 3-t-butyloxypentyl, 3-t-butyloxyhexyl, 3-t-butyloxy-4-methylpentyl, 3-t-butyloxyheptyl, 3-t-butyloxy-5-methylhexyl, 3-t-butyloxy-4,4-dimethylpentyl, 3-t-butyloxyoctyl, 3-t-butyloxy-5,5-dimethylhexyl, 3-n-pentyloxypropyl, 3-n-pentyloxybutyl, 3-n-pentyloxypentyl, 3-n-pentylxyhexyl, 3-n-pentyloxy-4-methylpentyl, 3-n-pentyloxyheptyl, 3-n-pentyloxy-5-methylhexyl, 3-n-pentyloxy-4,4-dimethylpentyl, 3-n-pentyloxyoctyl, or 3-n-pentyloxy-5,5-dimethylhexyl;

Z is ethylene or oxymethylene.

(Compound No., R⁶, R⁷, R⁸, R^E, Z)=(A13, F, F, Me, 1-methyloxyethyl, CH2CH2), (A14, F, F, Me, 1-methyloxypropyl, CH2CH2), (A15, F, F,. Me, 1-methyloxybutyl, CH2CH2), (A16, F, F, Me, 1-methyloxy-2-methylpropyl, CH2CH2), (A17, F, F, Me, 1-methyloxypentyl, CH2CH2), (A18, F, F, Me, 1-methyloxy-3-methylbutyl, CH2CH2), (A19, F, F, Me, 1-methyloxy-2,2-dimethylpropyl, CH2CH2), (A20, F, F, Me, 1-methyloxyhexyl, CH2CH2), (A21, F, F, Me, 1-methyloxy-3,3-dimethylbutyl, CH2CH2), (A22, F, F, Me, 1-ethyloxyethyl, CH2CH2), (A23, F, F, Me, 1-ethyloxypropyl, CH2CH2), (A24, F, F, Me, 1-ethyloxybutyl, CH2CH2), (A25, F, F, Me, 1-ethyloxy-2-methylpropyl, CH2CH2), (A26, F, F, Me, 1-ethyloxypentyl, CH2CH2), (A27, F, F, Me, 1-ethyloxy-3-methylbutyl, CH2CH2), (A28, F, F, Me, 1-ethyloxy-2,2-dimethylpropyl, CH2CH2), (A29, F, F, Me, 1-ethyloxyhexyl, CH2CH2), (A30, F, F, Me, 1-ethyloxy-3,3-dimethylbutyl, CH2CH2), (A31, F, F, Me, 1-n-propyloxyethyl, CH2CH2), (A32, F, F, Me, 1-n-propyloxypropyl, CH2CH2), (A33, F, F, Me, 1-n-propyloxybutyl, CH2CH2), (A34, F, F, Me, 1-n-propyloxy-2-methylpropyl, CH2CH2), (A35, F, F, Me, 1-n-propyloxypentyl, CH2CH2), (A36, F, F, Me, 1-n-propyloxy-3-methylbutyl, CH2CH2), (A37, F, F, Me, 1-n-propyloxy-2,2-dimethylpropyl, CH2CH2), (A38, F, F, Me, 1-n-propyloxyhexyl, CH2CH2), (A39, F, F, Me, 1-n-propyloxy-3,3-dimethylbutyl, CH2CH2), (A40, F, F, Me, 1-isopropyloxyethyl, CH2CH2), (A41, F, F, Me, 1-isopropyloxypropyl, CH2CH2), (A42, F, F, Me, 1-isopropyloxybutyl, CH2CH2), (A43, F, F, Me, 1-isopropyloxy-2-methylpropyl, CH2CH2), (A44, F, F, Me, 1-isopropyloxypentyl, CH2CH2), (A45, F, F, Me, 1-isopropyloxy-3-methylbutyl, CH2CH2), (A46, F, F, Me, 1-isopropyloxy-2,2-dimethylpropyl, CH2CH2), (A47, F, F, Me, 1-isopropyloxyhexyl, CH2CH2), (A48, F, F, Me, 1-isopropyloxy-3,3-dimethylbutyl, CH2CH2), (A49, F, F, Me, 1-n-butyloxyethyl, CH2CH2), (A50, F, F, Me, 1-n-butyloxypropyl, CH2CH2), (A51, F, F, Me, 1-n-butyloxybutyl, CH2CH2), (A52, F, F, Me, 1-n-butyloxy-2-methylpropyl, CH2CH2), (A53, F, F, Me, 1-n-butyloxypentyl, CH2CH2), (A54, F, F, Me, 1-n-butyloxy-3-methylbutyl, CH2CH2), (A55, F, F, Me, 1-n-butyloxy-2,2-dimethylpropyl, CH2CH2), (A56, F, F, Me, 1-n-butyloxyhexyl, CH2CH2), (A57, F, F, Me, 1-n-butyloxy-3,3-dimethylbutyl, CH2CH2), (A58, F, F, Me, 1-isobutyloxyethyl, CH2CH2), (A59, F, F, Me, 1-isobutyloxypropyl, CH2CH2), (A60, F, F, Me, 1-isobutyloxybutyl, CH2CH2), (A61, F, F, Me, 1-isobutyloxy-2-methylpropyl, CH2CH2), (A62, F, F, Me, 1-isobutyloxypentyl, CH2CH2), (A63, F, F, Me, 1-isobutyloxy-3-methylbutyl, CH2CH2), (A64, F, F, Me, 1-isobutyloxy-2,2-dimethylpropyl, CH2CH2), (A65, F, F, Me, 1-isobutyloxyhexyl, CH2CH2), (A66, F, F, Me, 1-isobutyloxy-3,3-dimethylbutyl, CH2CH2), (A67, F, F, Me, 1-t-butyloxyethyl, CH2CH2), (A68, F, F, Me, 1-t-butyloxypropyl, CH2CH2), (A69, F, F, Me, 1-t-butyloxybutyl, CH2CH2), (A70, F, F, Me, 1-t-butyloxy-2-methylpropyl, CH2CH2), (A71, F, F, Me, 1-t-butyloxypentyl, CH2CH2), (A72, F, F, Me, 1-t-butyloxy-3-methylbutyl, CH2CH2), (A73, F, F, Me, 1-t-butyloxy-2,2-dimethylpropyl, CH2CH2), (A74, F, F, Me, 1-t-butyloxyhexyl, CH2CH2), (A75, F. F, Me, 1-t-butyloxy-3,3-dimethylbutyl, CH2CH2), (A76, F, F, Me, 1-n-pentyloxyethyl, CH2CH2), (A77, F, F, Me, 1-n-pentyloxypropyl, CH2CH2), (A78, F, F, Me, 1-n-pentyloxybutyl, CH2CH2), (A79, F, F, Me, 1-n-pentyloxy-2-methylpropyl, CH2CH2), (A80, F, F, Me, 1-n-pentyloxypentyl, CH2CH2), (A81, F, F, Me, 1-n-pentyloxy-3-methylbutyl, CH2CH2), (A82, F, F, Me, 1-n-pentyloxy-2,2-dimethylpropyl, CH2CH2), (A83, F, F, Me, 1-n-pentyloxyhexyl, CH2CH2), (A84, F, F, Me, 1-n-pentyloxy-3,3-dimethylbutyl, CH2CH2), (A85, F, F, Me, 1-neopentyloxyethyl, CH2CH2), (A86, F, F, Me, 1-neopentyloxypropyl, CH2CH2), (A87, F, F, Me, 1-neopentyloxybutyl, CH2CH2), (A88, F, F, Me, 1-neopentyloxy-2-methylpropyl, CH2CH2), (A89, F, F, Me, 1-neopentyloxypentyl, C142CH2), (A90, F, F, Me, 1-neopentyloxy-3-methylbutyl, CH2CH2), (A91, F, F, Me, 1-neopentyloxy-2,2-dimethylpropyl, CH2CH2), (A92, F, F, Me, 1-neopentyloxyhexyl, CH2CH2), (A93, F, F, Me, 1-neopentyloxy-3,3-dimethylbutyl, CH2CH2), (A94, F, F, OMe, 1-methyloxyethyl, CH2CH2), (A95, F, F, OMe, 1-methyloxypropyl, CH2CH2), (A96, F, F, OMe, 1-methyloxybutyl, CH2CH2), (A97, F, F, OMe, 1-methyloxy-2-methylpropyl, CH2CH2), (A98, F, F, OMe, 1-methyloxypentyl, CH2CH2), (A99, F, F, OMe, 1-methyloxy-3-methylbutyl, CH2CH2), (A100, F, F, OMe, 1-methyloxy-2,2-dimethylpropyl, CH2CH2), (A101, F, F, OMe, 1-methyloxyhexyl, CH2CH2), (A102, F, F, OMe, 1-methyloxy-3,3-dimethylbutyl, CH2CH2), (A103, F, F, OMe, 1-ethyloxyethyl, CH2CH2), (A104, F, F, OMe, 1-ethyloxypropyl, CH2CH2), (A105, F, F, OMe, 1-ethyloxybutyl, CH2CH2), (A106, F, F, OMe, 1-ethyloxy-2-methylpropyl, CH2CH2), (A107, F, F, OMe, 1-ethyloxypentyl, CH2CH2), (A108, F, F, OMe, 1-ethyloxy-3-methylbutyl, CH2CH2), (A109, F, F, OMe, 1-ethyloxy-2,2-dimethylpropyl, CH2CH2), (AL110, F, F, OMe, 1-ethyloxyhexyl, CH2CH2), (A111, F, F, OMe, 1-ethyloxy-3,3-dimethylbutyl, CH2CH2), (A112, F, F, OMe, 1-n-propyloxyethyl, CH2CH2), (A113, F, F, OMe, 1-n-propyloxypropyl, CH2CH2), (A114, F, F, OMe, 1-n-propyloxybutyl, CH2CH2), (A115, F, F, OMe, 1-n-propyloxy-2-methylpropyl, CH2CH2), (A116, F, F, OMe, 1-n-propyloxypentyl, CH2CH2), (A117, F, F, OMe, 1-n-propyloxy-3-methylbutyl, CH2CH2), (A118, F, F, OMe, 1-n-propyloxy-2,2-dimethylpropyl, CH2CH2), (A119, F, F, OMe, 1-n-propyloxyhexyl, CH2CH2), (A120, F, F, OMe, 1-n-propyloxy-3,3-dimethylbutyl, CH2CH2), (A121, F, F, OMe, 1-isopropyloxyethyl, CH2CH2), (A122, F, F, OMe, 1-isopropyloxypropyl, CH2CH2), (A123, F, F, OMe, 1-isopropyloxybutyl, CH2CH2), (A124, F, F,. OMe, 1-isopropyloxy-2-methylpropyl, CH2CH2), (A125, F, F, OMe, 1-isopropyloxypentyl, CH2CH2), (A126, F, F, OMe, 1-isopropyloxy-3-methylbutyl, CH2CH2), (A127, F, F, OMe, 1-isopropyloxy-2,2-dimethylpropyl, CH2CH2), (A128, F, F, OMe, 1-isopropyloxyhexyl, CH2CH2), (A129, F, F, OMe, 1-isopropyloxy-3,3-dimethylbutyl, CH2CH2), (A130, F, F, OMe, 1-n-butyloxyethyl, CH2CH2), (A131, F, F, OMe, 1-n-butyloxypropyl, CH2CH2), (A132, F, F, OMe, 1-n-butyloxybutyl, CH2CH2), (A133, F, F, OMe, 1-n-butyloxy-2-methylpropyl, CH2CH2), (A134, F, F, OMe, 1-n-butyloxypentyl, CH2CH2), (A135, F, F, OMe, 1-n-butyloxy-3-methylbutyl, CH2CH2), (A136, F, F, OMe, 1-n-butyloxy-2,2-dimethylpropyl, CH2CH2), (A137, F, F, OMe, 1-n-butyloxyhexyl, CH2CH2), (A138, F, F, OMe, 1-n-butyloxy-3,3-dimethylbutyl, CH2CH2), (A139, F, F, OMe, 1-isobutyloxyethyl, CH2CH2), (A140, F, F, OMe, 1-isobutyloxypropyl, CH2CH2), (A141, F, F, OMe, 1-isobutyloxybutyl, CH2CH2), (A142, F, F, OMe, 1-isobutyloxy-2-methylpropyl, CH2CH2), (A143, F, F, OMe, 1-isobutyloxypentyl, CH2CH2), (A144, F, F, OMe, 1-isobutyloxy-3-methylbutyl, CH2CH2), (A145, F, F, OMe, 1-isobutyloxy-2,2-dimethylpropyl, CH2CH2), (A146, F, F, OMe, 1-isobutyloxyhexyl, CH2CH2), (A147, F, F, OMe, 1-isobutyloxy-3,3-dimethylbutyl, CH2CH2), (A148, F, F, OMe, 1-t-butyloxyethyl, CH2CH2), (A149, F, F, OMe, 1-t-butyloxypropyl, CH2CH2), (A150, F, F, OMe, 1-t-butyloxybutyl, CH2CH2), (A151, F, F, OMe, 1-t-butyloxy-2-methylpropyl, CH2CH2), (A152, F, F, OMe, 1-t-butyloxypentyl, CH2CH2), (A153, F, F, OMe, 1-t-butyloxy-3-methylbutyl, CH2CH2), (A154, F, F, OMe, 1-t-butyloxy-2,2-dimethylpropyl, CH2CH2), (A155, F, F, OMe, 1-t-butyloxyhexyl, CH2CH2), (A156, F, F, OMe, 1-t-butyloxy-3,3-dimethylbutyl, CH2CH2), (A157, F, F, OMe, 1-n-pentyloxyethyl, CH2CH2), (A158, F, F, OMe, 1-n-pentyloxypropyl, CH2CH2), (A159, F, F, OMe, 1-n-pentyloxybutyl, CH2CH2), (A160, F, F, OMe, 1-n-pentyloxy-2-methylpropyl, CH2CH2), (A161, F, F, OMe, 1-n-pentyloxypentyl, CH2CH2), (A162, F, F, OMe, 1-n-pentyloxy-3-methylbutyl, CH2CH2), (A163, F, F, OMe, 1-n-pentyloxy-2,2-dimethylpropyl, CH2CH2), (A164, F, F, OMe, 1-n-pentyloxyhexyl, CH2CH2), (A165, F, F, OMe, 1-n-pentyloxy-3,3-dimethylbutyl, CH2CH2), (A166, F, F, OMe, 1-neopentyloxyethyl, CH2CH2), (A167, F, F, OMe, 1-neopentyloxypropyl, CH2CH2), (A168, F, F, OMe, 1-neopentyloxybutyl, CH2CH2), (A169, F, F, OMe, 1-neopentyloxy-2-methylpropyl, CH2CH2), (A170, F, F, OMe, 1-neopentyloxypentyl, CH2CH2), (A171, F, F, OMe, 1-neopentyloxy-3-methylbutyl, CH2CH2), (A172, F, F, OMe, 1-neopentyloxy-2,2-dimethylpropyl, CH2CH2), (A173, F, F, OMe, 1-neopentyloxyhexyl, CH2CH2), (A174, F, F, OMe, 1-neopentyloxy-3,3-dimethylbutyl, CH2CH2), (A175, F, F, Me, 1-methyloxyethyl, OCH2), (A176, F, F, Me, 1-methyloxypropyl, OCH2), (A177, F, F, Me, 1-methyloxybutyl, OCH2), (A178, F, F, Me, 1-methyloxy-2-methylpropyl, OCH2), (A179, F, F, Me, 1-methyloxypentyl, OCH2), (A180, F, F, Me, 1-methyloxy-3-methylbutyl, OCH2), (A181, F, F, Me, 1-methyloxy-2,2-dimethylpropyl, OCH2), (A182, F, F, Me, 1-methyloxyhexyl, OCH2), (A183, F, F, Me, 1-methyloxy-3,3-dimethylbutyl, OCH2), (A184, F, F, Me, 1-ethyloxyethyl, OCH2), (A185, F, F, Me, 1-ethyloxypropyl, OCH2), (A186, F, F, Me, 1-ethyloxybutyl, OCH2), (A187, F, F, Me, 1-ethyloxy-2-methylpropyl, OCH2), (A188, F, F, Me, 1-ethyloxypentyl, OCH2), (A189, F, F, Me, 1-ethyloxy-3-methylbutyl, OCH2), (A190, F, F, Me, 1-ethyloxy-2,2-dimethylpropyl, OCH2), (A191, F, F, Me, 1-ethyloxyhexyl, OCH2), (A192, F, F, Me, 1-ethyloxy-3,3-dimethylbutyl, OCH2), (A193, F, F, Me, 1-n-propyloxyethyl, OCH2), (A194, F, F, Me, 1-n-propyloxypropyl, OCH2), (A195, F, F, Me, 1-n-propyloxybutyl, OCH2), (A196, F, F, Me, 1-n-propyloxy-2-methylpropyl, OCH2), (A197, F, F, Me, 1-n-propyloxypentyl, OCH2), (A198, F, F, Me, 1-n-propyloxy-3-methylbutyl, OCH2), (A199, F, F, Me, 1-n-propyloxy-2,2-dimethylpropyl, OCH2), (A200, F, F, Me, 1-n-propyloxyhexyl, OCH2), (A201, F, F, Me, 1-n-propyloxy-3,3-dimethylbutyl, OCH2), (A202, F, F, Me, 1-isopropyloxyethyl, OCH2), (A203, F, F, Me, 1-isopropyloxypropyl, OCH2), (A204, F, F, Me, 1-isopropyloxybutyl, OCH2), (A205, F, F, Me, 1-isopropyloxy-2-methylpropyl, OCH2), (A206, F, F, Me, 1-isopropyloxypentyl, OCH2), (A207, F, F, Me, 1-isopropyloxy-3-methylbutyl, OCH2), (A208, F, F, Me, 1-isopropyloxy-2,2-dimethylpropyl, OCH2), (A209, F, F, Me, 1-isopropyloxyhexyl, OCH2), (A210, F, F, Me, 1-isopropyloxy-3,3-dimethylbutyl, OCH2), (A211, F, F, Me, 1-n-butyloxyethyl, OCH2), (A212, F, F, Me, 1-n-butyloxypropyl, OCH2), (A213, F, F, Me, 1-n-butyloxybutyl, OCH2), (A214, F, F, Me, 1-n-butyloxy-2-methylpropyl, OCH2), (A215, F, F, Me, 1-n-butyloxypentyl, OCH2), (A216, F, F, Me, 1-n-butyloxy-3-methylbutyl, OCH2), (A217, F, F, Me, 1-n-butyloxy-2,2-dimethylpropyl, OCH2), (A218, F, F, Me, 1-n-butyloxyhexyl, OCH2), (A219, F, F, Me, 1-n-butyloxy-3,3-dimethylbutyl, OCH2), (A220, F, F, Me, 1-isobutyloxyethyl, OCH2), (A221, F, F, Me, 1-isobutyloxypropyl, OCH2), (A222, F, F, Me, 1-isobutyloxybutyl, OCH2), (A223, F, F, Me, 1-isobutyloxy-2-methylpropyl, OCH2), (A224, F, F, Me, 1-isobutyloxypentyl, OCH2), (A225, F, F, Me, 1-isobutyloxy-3-methylbutyl, OCH2), (A226, F, F, Me, 1-isobutyloxy-2,2-dimethylpropyl, OCH2), (A227, F, F, Me, 1-isobutyloxyhexyl, OCH2), (A228, F, F, Me, 1-isobutyloxy-3,3-dimethylbutyl, OCH2), (A229, F, F, Me, 1-t-butyloxyethyl, OCH2), (A230, F, F, Me, 1-t-butyloxypropyl, OCH2), (A231, F, F, Me, 1-t-butyloxybutyl, OCH2), (A232, F, F, Me, 1-t-butyloxy-2-methylpropyl, OCH2), (A233, F, F, Me, 1-t-butyloxypentyl, OCH2), (A234, F, F, Me, 1-t-butyloxy-3-methylbutyl, OCH2), (A235, F, F, Me, 1-t-butyloxy-2,2-dimethylpropyl, OCH2), (A236, F, F, Me, 1-t-butyloxyhexyl, OCH2), (A237, F, F, Me, 1-t-butyloxy-3,3-dimethylbutyl, OCH2), (A238, F, F, Me, 1-n-pentyloxyethyl, OCH2), (A239, F, F, Me, 1-n-pentyloxypropyl, OCH2), (A240, F, F, Me, 1-n-pentyloxybutyl, OCH2), (A241, F, F, Me, 1-n-pentyloxy-2-methylpropyl, OCH2), (A242, F, F, Me, 1-n-pentyloxypentyl, OCH2), (A243, F, F, Me, 1-n-pentyloxy-3-methylbutyl, OCH2), (A244, F, F, Me, 1-n-pentyloxy-2,2-dimethylpropyl, OCH2), (A245, F, F, Me, 1-n-pentyloxyhexyl, OCH2), (A246, F, F, Me, 1-n-pentyloxy-3,3-dimethylbutyl, OCH2), (A247, F, F, Me, 1-neopentyloxyethyl, OCH2), (A248, F, F, Me, 1-neopentyloxypropyl, OCH2), (A249, F, F, Me, 1-neopentyloxybutyl, OCH2), (A250, F, F, Me, 1-neopentyloxy-2-methylpropyl, OCH2), (A251, F, F, Me, 1-neopentyloxypentyl, OCH2), (A252, F, F, Me, 1-neopentyloxy-3-methylbutyl, OCH2), (A253, F, F, Me, 1-neopentyloxy-2,2-dimethylpropyl, OCH2), (A254, F, F, Me, 1-neopentyloxyhexyl, OCH2), (A255, F, F, Me, 1-neopentyloxy-3,3-dimethylbutyl, OCH2), (A256, F, F, OMe, 1-methyloxyethyl, OCH2), (A257, F, F, OMe, 1-methyloxypropyl, OCH2), (A258, F, F, OMe, 1-methyloxybutyl, OCH2), (A259, F, F, OMe, 1-methyloxy-2-methylpropyl, OCH2), (A260, F, F, OMe, 1-methyloxypentyl, OCH2), (A261, F, F, OMe, 1-methyloxy-3-methylbutyl, OCH2), (A262, F, F, OMe, 1-methyloxy-2,2-dimethylpropyl, OCH2), (A263, F, F, OMe, 1-methyloxyhexyl, OCH2), (A264, F, F, OMe, 1-methyloxy-3,3-dimethylbutyl, OCH2), (A265, F, F, OMe, 1-ethyloxyethyl, OCH2), (A266, F, F, OMe, 1-ethyloxypropyl, OCH2), (A267, F, F, OMe, 1-ethyloxybutyl, OCH2), (A268, F, F, OMe, 1-ethyloxy-2-methylpropyl, OCH2), (A269, F, F, OMe, 1-ethyloxypentyl, OCH2), (A270, F, F, OMe, 1-ethyloxy-3-methylbutyl, OCH2), (A271, F, F, OMe, 1-ethyloxy-2,2-dimethylpropyl, OCH2), (A272, F, F, OMe, 1-ethyloxyhexyl, OCH2), (A273, F, F, OMe, 1-ethyloxy-3,3-dimethylbutyl, OCH2), (A274, F, F, OMe, 1-n-propyloxyethyl, OCH2), (A275, F, F, OMe, 1-n-propyloxypropyl, OCH2), (A276, F, F, OMe, 1-n-propyloxybutyl, OCH2), (A277, F, F, OMe, 1-n-propyloxy-2-methylpropyl, OCH2), (A278, F, F, OMe, 1-n-propyloxypentyl, OCH2), (A279, F, F, OMe, 1-n-propyloxy-3-methylbutyl, OCH2), (A280, F, F, OMe, 1-n-propyloxy-2,2-dimethylpropyl, OCH2), (A281, F, F, OMe, 1-n-propyloxyhexyl, OCH2), (A282, F, F, OMe, 1-n-propyloxy-3,3-dimethylbutyl, OCH2), (A283, F, F, OMe, 1-isopropyloxyethyl, OCH2), (A284, F, F, OMe, 1-isopropyloxypropyl, OCH2), (A285, F, F, OMe, 1-isopropyloxybutyl, OCH2), (A286, F, F, OMe, 1-isopropyloxy-2-methylpropyl, OCH2), (A287, F, F, OMe, 1-isopropyloxypentyl, OCH2), (A288, F, F, OMe, 1-isopropyloxy-3-methylbutyl, OCH2), (A289, F, F, OMe, 1-isopropyloxy-2,2-dimethylpropyl, OCH2), (A290, F, F, OMe, 1-isopropyloxyhexyl, OCH2), (A291, F, F, OMe, 1-isopropyloxy-3,3-dimethylbutyl, OCH2), (A292, F, F, OMe, 1-n-butyloxyethyl, OCH2), (A293, F, F, OMe, 1-n-butyloxypropyl, OCH2), (A294, F, F, OMe, 1-n-butyloxybutyl, OCH2), (A295, F, F, OMe, 1-n-butyloxy-2-methylpropyl, OCH2), (A296, F, F, OMe, 1-n-butyloxypentyl, OCH2), (A297, F, F, OMe, 1-n-butyloxy-3-methylbutyl, OCH2), (A298, F, F, OMe, 1-n-butyloxy-2,2-dimethylpropyl, OCH2), (A299, F, F, OMe, 1-n-butyloxyhexyl, OCH2), (A300, F, F, OMe, 1-n-butyloxy-3,3-dimethylbutyl, OCH2), (A301, F, F, OMe, 1-isobutyloxyethyl, OCH2), (A302, F, F, OMe, 1-isobutyloxypropyl, OCH2), (A303, F, F, OMe, 1-isobutyloxybutyl, OCH2), (A304, F, F, OMe, 1-isobutyloxy-2-methylpropyl, OCH2), (A305, F, F, OMe, 1-isobutyloxypentyl, OCH2), (A306, F, F, OMe, 1-isobutyloxy-3-methylbutyl, OCH2), (A307, F, F, OMe, 1-isobutyloxy-2,2-dimethylpropyl, OCH2), (A308, F, F, OMe, 1-isobutyloxyhexyl, OCH2), (A309, F, F, OMe, 1-isobutyloxy-3,3-dimethylbutyl, OCH2), (A310, F, F, OMe, 1-t-butyloxyethyl, OCH2), (A311, F, F, OMe, 1-t-butyloxypropyl, OCH2), (A312, F, F, OMe, 1-t-butyloxybutyl, OCH2), (A313, F, F, OMe, 1-t-butyloxy-2-methylpropyl, OCH2), (A314, F, F, OMe, 1-t-butyloxypentyl, OCH2), (A315, F, F, OMe, 1-t-butyloxy-3-methylbutyl, OCH2), (A316, F, F, OMe, 1-t-butyloxy-2,2-dimethylpropyl, OCH2), (A317, F, F, OMe, 1-t-butyloxyhexyl, OCH2), (A318, F, F, OMe, 1-t-butyloxy-3,3-dimethylbutyl, OCH2), (A319, F, F, OMe, 1-n-pentyloxyethyl, OCH2), (A320, F, F, OMe, 1-n-pentyloxypropyl, OCH2), (A321, F, F, OMe, 1-n-pentyloxybutyl, OCH2), (A322, F, F, OMe, 1-n-pentyloxy-2-methylpropyl, OCH2), (A323, F, F, OMe, 1-n-pentyloxypentyl, OCH2), (A324, F, F, OMe, 1-n-pentyloxy-3-methylbutyl, OCH2), (A325, F, F, OMe, 1-n-pentyloxy-2,2-dimethylpropyl, OCH2), (A326, F, F, OMe, 1-n-pentyloxyhexyl, OCH2), (A327, F, F, OMe, 1-n-pentyloxy-3,3-dimethylbutyl, OCH2), (A328, F, F, OMe, 1-neopentyloxyethyl, OCH2), (A329, F, F, OMe, 1-neopentyloxypropyl, OCH2), (A330, F, F, OMe, 1-neopentyloxybutyl, OCH2), (A331, F, F, OMe, 1-neopentyloxy-2-methylpropyl, OCH2), (A332, F, F, OMe, 1-neopentyloxypentyl, OCH2), (A333, F, F, OMe, 1-neopentyloxy-3-methylbutyl, OCH2), (A334, F, F, OMe, 1-neopentyloxy-2,2-dimethylpropyl, OCH2), (A335, F, F, OMe, 1-neopentyloxyhexyl, OCH2), (A336, F, F, OMe, 1-neopentyloxy-3,3-dimethylbutyl, OCH2), (A337, F, F, Me, 3-methyloxypropyl, CH2CH2), (A338, F, F, Me, 3-methyloxybutyl, CH2CH2), (A340, F, F, Me, 3-methyloxy-4-methylpentyl, CH2CH2), (A342, F, F, Me, 3-methyloxy-5-methylhexyl, CH2CH2), (A343, F, F, Me, 3-methyloxyoctyl, CH2CH2), (A344, F, F, Me, 3-methyloxy-5,5-dimethylhexyl, CH2CH2), (A345, F, F, Me, 3-ethyloxybutyl, CH2CH2), (A348, F, F, Me, 3-ethyloxy-4-methylpentyl, CH2CH2), (A350, F, F, Me, 3-ethyloxy-5-methylhexyl, CH2CH2), (A352, F, F, Me, 3-ethyloxyoctyl, CH2CH2), (A353, F, F, Me, 3-ethyloxy-5,5-dimethylhexyl, CH2CH2), (A354, F, F, Me, 3-n-propyloxybutyl, CH2CH2), (A355, F, F, Me, 3-n-propyloxypentyl, CH2CH2), (A356, F, F, Me, 3-n-propyloxyhexyl, CH2CH2), (A357, F, F, Me, 3-n-propyloxy-4-methylpentyl, CH2CH2), (A358, F, F, Me, 3-n-propyloxyheptyl, CH2CH2), (A359, F, F, Me, 3-n-propyloxy-5-methylhexyl, CH2CH2), (A360, F, F, Me, 3-n-propyloxy-4,4-dimethylpentyl, CH2CH2), (A361, F, F, Me, 3-n-propyloxyoctyl, CH2CH2), (A362, F, F, Me, 3-n-propyloxy-5,5-dimethylhexyl, CH2CH2), (A363, F, F, Me, 3-isopropyloxybutyl, CH2CH2), (A364, F, F, Me, 3-isopropyloxypentyl, CH2CH2), (A365, F, F, Me, 3-isopropyloxyhexyl, CH2CH2), (A366, F, F, Me, 3-isopropyloxy-4-methylpentyl, CH2CH2), (A367, F, F, Me, 3-isopropyloxyheptyl, CH2CH2), (A368, F, F, Me, 3-isopropyloxy-5-methylhexyl, CH2CH2), (A369, F, F, Me, 3-isopropyloxy-4,4-dimethylpentyl, CH2CH2), (A370, F, F, Me, 3-isopropyloxyoctyl, CH2CH2), (A371, F, F, Me, 3-isopropyloxy-5,5-dimethylhexyl, CH2CH2), (A372, F, F, Me, 3-n-butyloxybutyl, CH2CH2), (A373, F, F, Me, 3-n-butyloxypentyl, CH2CH2), (A374, F, F, Me, 3-n-butyloxyhexyl, CH2CH2), (A375, F, F, Me, 3-n-butyloxy-4-methylpentyl, CH2CH2), (A376, F, F, Me, 3-n-butyloxyheptyl, CH2CH2), (A377, F, F, Me, 3-n-butyloxy-5-methylhexyl, CH2CH2), (A378, F, F, Me, 3-n-butyloxy-4,4-dimethylpentyl, CH2CH2), (A379, F, F, Me, 3-n-butyloxyoctyl, CH2CH2), (A380, F, F, Me, 3-n-butyloxy-5,5-dimethylhexyl, CH2CH2), (A381, F, F, Me, 3-isobutyloxypropyl, CH2CH2), (A382, F, F, Me, 3-isobutyloxybutyl, CH2CH2), (A383, F, F, Me, 3-isobutyloxypentyl, CH2CH2), (A384, F, F, Me, 3-isobutyloxyhexyl, CH2CH2), (A385, F, F, Me, 3-isobutyloxy-4-methylpentyl, CH2CH2), (A386, F, F, Me, 3-isobutyloxyheptyl, CH2CH2), (A387, F, F, Me, 3-isobutyloxy-5-methylhexyl, CH2CH2), (A388, F, F, Me, 3-isobutyloxy-4,4-dimethylpentyl, CH2CH2), (A389, F, F, Me, 3-isobutyloxyoctyl, CH2CH2), (A390, F, F, Me, 3-isobutyloxy-5,5-dimethylhexyl, CH2CH2), (A391, F, F, Me, 3-t-butyloxypropyl, CH2CH2), (A392, F, F, Me, 3-t-butyloxybutyl, CH2CH2), (A393, F, F, Me, 3-t-butyloxypentyl, CH2CH2), (A394, F, F, Me, 3-t-butyloxyhexyl, CH2CH2), (A395, F, F, Me, 3-t-butyloxy-4-methylpentyl, CH2CH2), (A396, F, F, Me, 3-t-butyloxyheptyl, CH2CH2), (A397, F, F, Me, 3-t-butyloxy-5-methylhexyl, CH2CH2), (A398, F, F, Me, 3-t-butyloxy-4,4-dimethylpentyl, CH2CH2), (A399, F, F, Me, 3-t-butyloxyoctyl, CH2CH2), (A400, F, F, Me, 3-t-butyloxy-5,5-dimethylhexyl, CH2CH2), (A402, F, F, Me, 3-n-pentyloxybutyl, CH2CH2), (A403, F, F, Me, 3-n-pentyloxypentyl, CH2CH2), (A404, F, F, Me, 3-n-pentyloxyhexyl, CH2CH2), (A405, F, F, Me, 3-n-pentyloxy-4-methylpentyl, CH2CH2), (A406, F, F, Me, 3-n-pentyloxyheptyl, CH2CH2), (A407, F, F, Me, 3-n-pentyloxy-5-methylhexyl, CH2CH2), (A408, F, F, Me, 3-n-pentyloxy-4,4-dimethylpentyl, CH2CH2), (A409, F, F, Me, 3-n-pentyloxyoctyl, CH2CH2), (A410, F, F, Me, 3-n-pentyloxy-5,5-dimethylhexyl, CH2CH2), (A411, F, F, Me, 3-neopentyloxybutyl, CH2CH2), (A412, F, F, Me, 3-neopentyloxypentyl, CH2CH2), (A413, F, F, Me, 3-neopentyloxyhexyl, CH2CH2), (A414, F, F, Me, 3-neopentyloxy-4-methylpentyl, CH2CH2), (A415, F, F, Me, 3-neopentyloxyheptyl, CH2CH2), (A416, F, F, Me, 3-neopentyloxy-5-methylhexyl, CH2CH2), (A417, F, F, Me, 3-neopentyloxy-4,4-dimethylpentyl, CH2CH2), (A418, F, F, Me, 3-neopentyloxyoctyl, CH2CH2), (A419, F, F, Me, 3-neopentyloxy-5,5-dimethylhexyl, CH2CH2), (A420, F, F, OMe, 3-methyloxypropyl, CH2CH2), (A421, F, F, OMe, 3-methyloxybutyl, CH2CH2), (A422, F, F, OMe, 3-methyloxypentyl, CH2CH2), (A424, F, F, OMe, 3-methyloxy-4-methylpentyl, CH2CH2), (A425, F, F, OMe, 3-methyloxyheptyl, CH2CH2), (A426, F, F, OMe, 3-methyloxy-5-methylhexyl, CH2CH2), (A427, F, F, OMe, 3-metoxy-4,4-dimethylpentyl, CH2CH2), (A428, F, F, OMe, 3-methyloxyoctyl, CH2CH2), (A429, F, F, OMe, 3-methyloxy-5,5-dimethylhexyl, CH2CH2), (A431, F, F, OMe, 3-ethyloxybutyl, CH2CH2), (A432, F, F, OMe, 3-ethyloxypentyl, CH2CH2), (A433, F, F, OMe, 3-ethyloxyhexyl, CH2CH2), (A434, F, F, OMe, 3-ethyloxy-4-methylpentyl, CH2CH2), (A435, F, F, OMe, 3-ethyloxyheptyl, CH2CH2), (A436, F, F, OMe, 3-ethyloxy-5-methylhexyl, CH2CH2), (A437, F, F, OMe, 3-ethyloxy-4,4-dimethylpentyl, CH2CH2), (A438, F, F, OMe, 3-ethyloxyoctyl, CH2CH2), (A439, F, F, OMe, 3-ethyloxy-5,5-dimethylhexyl, CH2CH2), (A441, F, F, OMe, 3-n-propyloxybutyl, CH2CH2), (A442, F, F, OMe, 3-n-propyloxypentyl, CH2CH2), (A443, F, F, OMe, 3-n-propyloxyhexyl, CH2CH2), (A444, F, F, OMe, 3-n-propyloxy-4-methylpentyl, CH2CH2), (A445, F, F, OMe, 3-n-propyloxyheptyl, CH2CH2), (A446, F, F, OMe, 3-n-propyloxy-5-methylhexyl, CH2CH2), (A447, F, F, OMe, 3-n-propyloxy-4,4-dimethylpentyl, CH2CH2), (A448, F, F, OMe, 3-n-propyloxyoctyl, CH2CH2), (A449, F, F, OMe, 3-n-propyloxy-5,5-dimethylhexyl, CH2CH2), (A451, F, F, OMe, 3-isopropyloxybutyl, CH2CH2), (A452, F, F, OMe, 3-isopropyloxypentyl, CH2CH2), (A453, F, F, OMe, 3-isopropyloxyhexyl, CH2CH2), (A454, F, F, OMe, 3-isopropyloxy-4-methylpentyl, CH2CH2), (A455, F, F, OMe, 3-isopropyloxyheptyl, CH2CH2), (A456, F, F, OMe, 3-isopropyloxy-5-methylhexyl, CH2CH2), (A457, F, F, OMe, 3-isopropyloxy-4,4-dimethylpentyl, CH2CH2), (A458, F, F, OMe, 3-isopropyloxyoctyl, CH2CH2), (A459, F, F, OMe, 3-isopropyloxy-5,5-dimethylhexyl, CH2CH2), (A460, F, F, OMe, 3-n-butyloxypropyl, CH2CH2), (A461, F, F, OMe, 3-n-butyloxybutyl, CH2CH2), (A462, F, F, OMe, 3-n-butyloxypentyl, CH2CH2), (A463, F, F, OMe, 3-n-butyloxyhexyl, CH2CH2), (A464, F, F, OMe, 3-n-butyloxy-4-methylpentyl, CH2CH2), (A465, F, F, OMe, 3-n-butyloxyheptyl, CH2CH2), (A466, F, F, OMe, 3-n-butyloxy-5-methylhexyl, CH2CH2), (A467, F, F, OMe, 3-n-butyloxy-4,4-dimethylpentyl, CH2CH2), (A468, F, F, OMe, 3-n-butyloxyoctyl, CH2CH2), (A469, F, F, OMe, 3-n-butyloxy-5,5-dimethylhexyl, CH2CH2), (A470, F, F, OMe, 3-isobutyloxypropyl, CH2CH2), (A471, F, F, OMe, 3-isobutyloxybutyl, CH2CH2), (A472, F, F, OMe, 3-isobutyloxypentyl, CH2CH2), (A473, F, F, OMe, 3-isobutyloxyhexyl, CH2CH2), (A474, F, F, OMe, 3-isobutyloxy-4-methylpentyl, CH2CH2), (A475, F, F, OMe, 3-isobutyloxyheptyl, CH2CH2), (A476, F, F. OMe, 3-isobutyloxy-5-methylhexyl, CH2CH2), (A477, F, F, OMe, 3-isobutyloxy-4,4-dimethylpentyl, CH2CH2), (A478, F, F, OMe, 3-isobutyloxyoctyl, CH2CH2), (A479, F, F, OMe, 3-isobutyloxy-5,5-dimethylhexyl, CH2CH2), (A480, F, F, OMe, 3-t-butyloxypropyl, CH2CH2), (A481, F, F, OMe, 3-t-butyloxybutyl, CH2CH2), (A482, F, F, OMe, 3-t-butyloxypentyl, CH2CH2), (A483, F, F, OMe, 3-t-butyloxyhexyl, CH2CH2), (A484, F, F, OMe, 3-t-butyloxy-4-methylpentyl, CH2CH2), (A485, F, F, OMe, 3-t-butyloxyheptyl, CH2CH2), (A486, F, F, OMe, 3-t-butyloxy-5-methylhexyl, CH2CH2), (A487, F, F, OMe, 3-t-butyloxy-4,4-dimethylpentyl, CH2CH2), (A488, F, F, OMe, 3-t-butyloxyoctyl, CH2CH2), (A489, F, F, OMe, 3-t-butyloxy-5,5-dimethylhexyl, CH2CH2), (A490, F, F, OMe, 3-n-pentyloxypropyl, CH2CH2), (A491, F, F, OMe, 3-n-pentyloxybutyl, CH2CH2), (A492, F, F, OMe, 3-n-pentyloxypentyl, CH2CH2), (A493, F, F, OMe, 3-n-pentyloxyhexyl, CH2CH2), (A494, F, F, OMe, 3-n-pentyloxy-4-methylpentyl, CH2CH2), (A495, F, F, OMe, 3-n-pentyloxyheptyl, CH2CH2), (A496, F, F, OMe, 3-n-pentyloxy-5-methylhexyl, CH2CH2), (A497, F, F, OMe, 3-n-pentyloxy-4,4-dimethylpentyl, CH2CH2), (A498, F, F, OMe, 3-n-pentyloxyoctyl, CH2CH2), (A499, F, F, OMe, 3-n-pentyloxy-5,5-dimethylhexyl, CH2CH2), (A501, F, F, OMe, 3-neopentyloxybutyl, CH2CH2), (A502, F, F, OMe, 3-neopentyloxypentyl, CH2CH2), (A503, F, F, OMe, 3-neopentyloxyhexyl, CH2CH2), (A504, F, F, OMe, 3-neopentyloxy-4-methylpentyl, CH2CH2), (A505, F, F, OMe, 3-neopentyloxyheptyl, CH2CH2), (A506, F, F, OMe, 3-neopentyloxy-5-methylhexyl, CH2CH2), (A507, F, F, OMe, 3-neopentyloxy-4,4-dimethylpentyl, CH2CH2), (A508, F, F, OMe, 3-neopentyloxyoctyl, CH2CH2), (A509, F, F, OMe, 3-neopentyloxy-5,5-dimethylhexyl, CH2CH2), (A510, F, F, OMe, 3-methyloxypropyl, OCH2), (A511, F, F, OMe, 3-methyloxybutyl, OCH2), (A512, F, F, OMe, 3-methyloxypentyl, OCH2), (A513, F, F, OMe, 3-methyloxyhexyl, OCH2), (A514, F, F, OMe, 3-methyloxy-4-methylpentyl, OCH2), (A515, F, F, OMe, 3-methyloxyheptyl, OCH2), (A516, F, F, OMe, 3-methyloxy-5-methylhexyl, OCH2), (A517, F, F, OMe, 3-metoxy-4,4-dimethylpentyl, OCH2), (A518, F, F, OMe, 3-methyloxyoctyl, OCH2), (A519, F, F, OMe, 3-methyloxy-5,5-dimethylhexyl, OCH2), (A520, F, F, OMe, 3-ethyloxypropyl, OCH2), (A521, F, F, OMe, 3-ethyloxybutyl, OCH2), (A522, F, F, OMe, 3-ethyloxypentyl, OCH2), (A523, F, F, OMe, 3-ethyloxyhexyl, OCH2), (A524, F, F, OMe, 3-ethyloxy-4-methylpentyl, OCH2), (A525, F, F, OMe, 3-ethyloxyheptyl, OCH2), (A526, F, F, OMe, 3-ethyloxy-5-methylhexyl, OCH2), (A527, F, F, OMe, 3-ethyloxy-4,4-dimethylpentyl, OCH2), (A528, F, F, OMe, 3-ethyloxyoctyl, OCH2), (A529, F, F, OMe, 3-ethyloxy-5,5-dimethylhexyl, OCH2), (A530, F, F, OMe, 3-n-propyloxypropyl, OCH2), (A531, F, F, OMe, 3-n-propyloxybutyl, OCH2), (A532, F, F, OMe, 3-n-propyloxypentyl, OCH2), (A533, F, F, OMe, 3-n-propyloxyhexyl, OCH2), (A534, F, F, OMe, 3-n-propyloxy-4-methylpentyl, OCH2), (A535, F, F, OMe, 3-n-propyloxyheptyl, OCH2), (A536, F, F, OMe, 3-n-propyloxy-5-methylhexyl, OCH2), (A537, F, F, OMe, 3-n-propyloxy-4,4-dimethylpentyl, OCH2), (A538, F, F, OMe, 3-n-propyloxyoctyl, OCH2), (A539, F, F, OMe, 3-n-propyloxy-5,5-dimethylhexyl, OCH2), (A540, F, F, OMe, 3-isopropyloxypropyl, OCH2), (A541, F, F, OMe, 3-isopropyloxybutyl, OCH2), (A542, F, F, OMe, 3-isopropyloxypentyl, OCH2), (A543, F, F, OMe, 3-isopropyloxyhexyl, OCH2), (A544, F, F, OMe, 3-isopropyloxy-4-methylpentyl, OCH2), (A545, F, F, OMe, 3-isopropyloxyheptyl, OCH2), (A546, F, F, OMe, 3-isopropyloxy-5-methylhexyl, OCH2), (A547, F, F, OMe, 3-isopropyloxy-4,4-dimethylpentyl, OCH2), (A548, F, F, OMe, 3-isopropyloxyoctyl, OCH2), (A549, F, F, OMe, 3-isopropyloxy-5,5-dimethylhexyl, OCH2), (A550, F, F, OMe, 3-n-butyloxypropyl, OCH2), (A551, F, F, OMe, 3-n-butyloxybutyl, OCH2), (A552, F, F, OMe, 3-n-butyloxypentyl, OCH2), (A553, F, F, OMe, 3-n-butyloxyhexyl, OCH2), (A554, F, F, OMe, 3-n-butyloxy-4-methylpentyl, OCH2), (A555, F, F, OMe, 3-n-butyloxyheptyl, OCH2), (A556, F, F, OMe, 3-n-butyloxy-5-methylhexyl, OCH2), (A557, F, F, OMe, 3-n-butyloxy-4,4-dimethylpentyl, OCH2), (A558, F, F, OMe, 3-n-butyloxyoctyl, OCH2), (A559, F, F, OMe, 3-n-butyloxy-5,5-dimethylhexyl, OCH2), (A560, F, F, OMe, 3-isobutyloxypropyl, OCH2), (A561, F, F, OMe, 3-isobutyloxybutyl, OCH2), (A562, F, F, OMe, 3-isobutyloxypentyl, OCH2), (A563, F, F, OMe, 3-isobutyloxyhexyl, OCH2), (A564, F, F, OMe, 3-isobutyloxy-4-methylpentyl, OCH2), (A565, F, F, OMe, 3-isobutyloxyheptyl, OCH2), (A566, F, F, OMe, 3-isobutyloxy-5-methylhexyl, OCH2), (A567, F, F, OMe, 3-isobutyloxy-4,4-dimethylpentyl, OCH2), (A568, F, F, OMe, 3-isobutyloxyoctyl, OCH2), (A569, F, F, OMe, 3-isobutyloxy-5,5-dimethylhexyl, OCH2), (A570, F, F, OMe, 3-t-butyloxypropyl, OCH2), (A571, F, F, OMe, 3-t-butyloxybutyl, OCH2), (A572, F, F. OMe, 3-t-butyloxypentyl, OCH2), (A573, F, F, OMe, 3-t-butyloxyhexyl, OCH2), (A574, F, F, OMe, 3-t-butyloxy-4-methylpentyl, OCH2), (A575, F, F, OMe, 3-t-butyloxyheptyl, OCH2), (A576, F, F, OMe, 3-t-butyloxy-5-methylhexyl, OCH2), (A577, F, F, OMe, 3-t-butyloxy-4,4-dimethylpentyl, OCH2), (A578, F, F, OMe, 3-t-butyloxyoctyl, OCH2), (A579, F, F, OMe, 3-t-butyloxy-5,5-dimethylhexyl, OCH2), (A580, F, F, OMe, 3-n-pentyloxypropyl, OCH2), (A581, F, F, OMe, 3-n-pentyloxybutyl, OCH2), (A582, F, F, OMe, 3-n-pentyloxypentyl, OCH2), (A583, F, F, OMe, 3-n-pentyloxyhexyl, OCH2), (A584, F, F, OMe, 3-n-pentyloxy-4-methylpentyl, OCH2), (A585, F, F, OMe, 3-n-pentyloxyheptyl, OCH2), (A586, F, F, OMe, 3-n-pentyloxy-5-methylhexyl, OCH2), (A587, F, F, OMe, 3-n-pentyloxy-4,4-dimethylpentyl, OCH2), (A588, F, F, OMe, 3-n-pentyloxyoctyl, OCH2), (A589, F, F, OMe, 3-n-pentyloxy-5,5-dimethylhexyl: OCH2), (A590, F, F, OMe, 3-neopentyloxypropyl, OCH2), (A591, F, F, OMe, 3-neopentyloxybutyl, OCH4), (A592, F, F, OMe, 3-neopentyloxypentyl, OCH2), (A593, F, F, OMe, 3-neopentyloxyhexyl, OCH2), (A594, F, F, OMe, 3-neopentyloxy-4-methylpentyl, OCH2), (A595, F, F, OMe, 3-neopentyloxyheptyl, OCH2), (A596, F, F, OMe, 3-neopentyloxy-5-methylhexyl, OCH2), (A597, F, F, OMe, 3-neopentyloxy-4,4-dimethylpentyl, OCH2), (A598, F, F, OMe, 3-neopentyloxyoctyl, OCH2), (A599, F, F, OMe, 3-neopentyloxy-5,5-dimethylhexyl, OCH2), (A600, Cl, Cl, Me, n-pentyl, CH2CH2), (A602, Cl, Cl, Me, 1-methyloxyethyl, CH2CH2), (A603, Cl, Cl, Me, 1-methyloxypropyl, CH2CH2), (A604, Cl, Cl, Me, 1-methyloxybutyl, CH2CH2), (A605, Cl, Cl, Me, 1-methyloxy-2-methylpropyl, CH2CH2), (A606, Cl, Cl, Me, 1-methyloxypentyl, CH2CH2), (A607, Cl, Cl, Me, 1-methyloxy-3-methylbutyl, CH2CH2), (A608, Cl, Cl, Me, 1-methyloxy-2,2-dimethylpropyl, CH2CH2), (A609, Cl, Cl, Me, 1-methyloxyhexyl, CH2CH2), (A610, Cl, Cl, Me, 1-methyloxy-3,3-dimethylbutyl, CH2CH2), (A611, Cl, Cl, Me, 1-ethyloxyethyl, CH2CH2), (A612, Cl, Cl, Me, 1-ethyloxypropyl, CH2CH2), (A613, Cl, Cl, Me, 1-ethyloxybutyl, CH2CH2), (A614, Cl, Cl, Me, 1-ethyloxy-2-methylpropyl, CH2CH2), (A615, Cl, Cl, Me, 1-ethyloxypentyl, CH2CH2), (A616, Cl, Cl, Me, 1-ethyloxy-3-methylbutyl, CH2CH2), (A617, Cl, Cl, Me, 1-ethyloxy-2,2-dimethylpropyl, CH2CH2), (A618, Cl, Cl, Me, 1-ethyloxyhexyl, CH2CH2), (A619, Cl, Cl, Me, 1-ethyloxy-3,3-dimethylbutyl, CH2CH2), (A620, Cl, Cl, Me, 1-n-propyloxyethyl, CH2CH2), (A621, Cl, Cl, Me, 1-n-propyloxypropyl, CH2CH2), (A622, Cl, Cl, Me, 1-n-propyloxybutyl, CH2CH2), (A623, Cl, Cl, Me, 1-n-propyloxy-2-methylpropyl, CH2CH2), (A624, Cl, Cl, Me, 1-n-propyloxypentyl, CH2CH2), (A625, Cl, Cl, Me, 1-n-propyloxy-3-methylbutyl, CH2CH2), (A626, Cl, Cl, Me, 1-n-propyloxy-2,2-dimethylpropyl, CH2CH2), (A627, Cl, Cl, Me, 1-n-propyloxy-n-hexyl, CH2CH2), (A628, Cl, Cl, Me, 1-n-propyloxy-3,3-dimethylbutyl, CH2CH2), (A629, Cl, Cl, Me, 1-isopropyloxyethyl, CH2CH2), (A630, Cl, Cl, Me, 1-isopropyloxypropyl, CH2CH2), (A631, Cl, Cl, Me, 1-isopropyloxybutyl, CH2CH2), (A632, Cl, Cl, Me, 1-isopropyloxy-2-methylpropyl, CH2CH2), (A633, Cl, Cl, Me, 1-isopropyloxypentyl, CH2CH2), (A634, Cl, Cl, Me, 1-isopropyloxy-3-methylbutyl, CH2CH2), (A635, Cl, Cl, Me, 1-isopropyloxy-2,2-dimethylpropyl, CH2CH2), (A636, Cl, Cl, Me, 1-isopropyloxyhexyl, CH2CH2), (A637, Cl, Cl, Me, 1-isopropyloxy-3,3-dimethylbutyl, CH2CH2), (A638, Cl, Cl, Me, 1-n-butyloxyethyl, CH2CH2), (A639, Cl, Cl, Me, 1-n-butyloxypropyl, CH2CH2), (A640, Cl, Cl, Me, 1-n-butyloxybutyl, CH2CH2), (A641, Cl, Cl, Me, 1-n-butyloxy-2-methylpropyl, CH2CH2), (A642, Cl, Cl, Me, 1-n-butyloxypentyl, CH2CH2), (A643, Cl, Cl, Me, 1-n-butyloxy-3-methylbutyl, CH2CH2), (A644, Cl, Cl, Me, 1-n-butyloxy-2,2-dimethylpropyl, CH2CH2), (A645, Cl, Cl, Me, 1-n-butyloxyhexyl, CH2CH2), (A646, Cl, Cl, Me, 1-n-butyloxy-3,3-dimethylbutyl, CH2CH2), (A647, Cl, Cl, Me, 1-isobutyloxyethyl, CH2CH2), (A648, Cl, Cl, Me, 1-isobutyloxypropyl, CH2CH2), (A649, Cl, Cl, Me, 1-isobutyloxybutyl, CH2CH2), (A650, Cl, Cl, Me, 1-isobutyloxy-2-methylpropyl, CH2CH2), (A651, Cl, Cl, Me, 1-isobutyloxypentyl, CH2CH2), (A652, Cl, Cl, Me, 1-isobutyloxy-3-methylbutyl, CH2CH2), (A653, Cl, Cl, Me, 1-isobutyloxy-2,2-dimethylpropyl, CH2CH2), (A654, Cl, Cl, Me, 1-isobutyloxyhexyl, CH2CH2), (A655, Cl, Cl, Me, 1-isobutyloxy-3,3-dimethylbutyl, CH2CH2), (A656, Cl, Cl, Me, 1-t-butyloxyethyl, CH2CH2), (A657, Cl, Cl, Me, 1-t-butyloxypropyl, CH2CH2), (A658, Cl, Cl, Me, 1-t-butyloxybutyl, CH2CH2), (A659, Cl, Cl, Me, 1-t-butyloxy-2-methylpropyl, CH2CH2), (A660, Cl, Cl, Me, 1-t-butyloxypentyl, CH2CH2), (A661, Cl, Cl, Me, 1-t-butyloxy-3-methylbutyl, CH2CH2), (A662, Cl, Cl, Me, 1-t-butyloxy-2,2-dimethylpropyl, CH2CH2), (A663, Cl, Cl, Me, 1-t-butyloxyhexyl, CH2CH2), (A664, Cl, Cl, Me, 1-t-butyloxy-3,3-dimethylbutyl, CH2CH2), (A665, Cl, Cl, Me, 1-n-pentyloxyethyl, CH2CH2), (A666, Cl, Cl, Me, 1-n-pentyloxypropyl, CH2CH2), (A667, Cl, Cl, Me, 1-n-pentyloxybutyl, CH2CH2), (A668, Cl, Cl, Me, 1-n-pentyloxy-2-methylpropyl, CH2CH2), (A669, Cl, Cl, Me, 1-n-pentyloxypentyl, CH2CH2), (A670, Cl, Cl, Me, 1-n-pentyloxy-3-methylbutyl, CH2CH2), (A671, Cl, Cl, Me, 1-n-pentyloxy-2,2-dimethylpropyl, CH2CH2), (A672, Cl, Cl, Me, 1-n-pentyloxyhexyl, CH2CH2), (A673, Cl, Cl, Me, 1-n-pentyloxy-3,3-dimethylbutyl, CH2CH2), (A674, Cl, Cl, Me, 1-neopentyloxyethyl, CH2CH2), (A675, Cl, Cl, Me, 1-neopentyloxypropyl, CH2CH2), (A676, Cl, Cl, Me, 1-neopentyloxybutyl, CH2CH2), (A677, Cl, Cl, Me, 1-neopentyloxy-2-methylpropyl, CH2CH2), (A678, Cl, Cl, Me, 1-neopentyloxypentyl, CH2CH2), (A679, Cl, Cl, Me, 1-neopentyloxy-3-methylbutyl, CH2CH2), (A680, Cl, Cl, Me, 1-neopentyloxy-2,2-dimethylpropyl, CH2CH2), (A681, Cl, Cl, Me, 1-neopentyloxyhexyl, CH2CH2), (A682, Cl, Cl, Me, 1-neopentyloxy-3,3-dimethylbutyl, CH2CH2), (A683, Cl, Cl, OMe, 1-methyloxyethyl, CH2CH2), (A684, Cl, Cl, OMe, 1-methyloxypropyl, CH2CH2), (A685, Cl, Cl, OMe, 1-methyloxybutyl, CH2CH2), (A686, Cl, Cl, OMe, 1-methyloxy-2-methylpropyl, CH2CH2), (A687, Cl, Cl, OMe, 1-methyloxypentyl, CH2CH2), (A688, Cl, Cl, OMe, 1-methyloxy-3-methylbutyl, CH2CH2), (A689, Cl, Cl, OMe, 1-methyloxy-2,2-dimethylpropyl, CH2CH2), (A690, Cl, Cl, OMe, 1-methyloxyhexyl, CH2CH2), (A691, Cl, Cl, OMe, 1-methyloxy-3,3-dimethylbutyl, CH2CH2), (A692, Cl, Cl, OMe, 1-ethyloxyethyl, CH2CH2), (A693, Cl, Cl, OMe, 1-ethyloxypropyl, CH2CH2), (A694, Cl, Cl, OMe, 1-ethyloxybutyl, CH2CH2), (A695, Cl, Cl, OMe, 1-ethyloxy-2-methylpropyl, CH2CH2), (A696, Cl, Cl, OMe, 1-ethyloxypentyl, CH2CH2), (A697, Cl, Cl, OMe, 1-ethyloxy-3-methylbutyl, CH2CH2), (A698, Cl, Cl, OMe, 1-ethyloxy-2,2-dimethylpropyl, CH2CH2), (A699, Cl, Cl, OMe, 1-ethyloxyhexyl, CH2CH2), (A700, Cl, Cl, OMe, 1-ethyloxy-3,3-dimethylbutyl, CH2CH2), (A701, Cl, Cl, OMe, 1-n-propyloxyethyl, CH2CH2), (A702, Cl, Cl, OMe, 1-n-propyloxypropyl, CH2CH2), (A703, Cl, Cl, OMe, 1-n-propyloxybutyl, CH2CH2), (A704, Cl, Cl, OMe, 1-n-propyloxy-2-methylpropyl, CH2CH2), (A705, Cl, Cl, OMe, 1-n-propyloxypentyl, CH2CH2), (A706, Cl, Cl, OMe, 1-n-propyloxy-3-methylbutyl, CH2CH2), (A707, Cl, Cl, OMe, 1-n-propyloxy-2,2-dimethylpropyl, CH2CH2), (A708, Cl, Cl, OMe, 1-n-propyloxy-n-hexyl, CH2CH2), (A709, Cl, Cl, OMe, 1-n-propyloxy-3,3-dimethylbutyl, CH2CH2), (A710, Cl, Cl, OMe, 1-isopropyloxyethyl, CH2CH2), (A711, Cl, Cl, OMe, 1-isopropyloxypropyl, CH2CH2), (A712, Cl, Cl, OMe, 1-isopropyloxybutyl, CH2CH2), (A713, Cl, Cl, OMe, 1-isopropyloxy-2-methylpropyl, CH2CH2), (A714, Cl, Cl, OMe, 1-isopropyloxypentyl, CH2CH2), (A715, Cl, Cl, OMe, 1-isopropyloxy-3-methylbutyl, CH2CH2), (A716, Cl, Cl, OMe, 1-isopropyloxy-2,2-dimethylpropyl, CH2CH2), (A717, Cl, Cl, OMe, 1-isopropyloxyhexyl, CH2CH2), (A718, Cl, Cl, OMe, 1-isopropyloxy-3,3-dimethylbutyl, CH2CH2), (A719, Cl, Cl, OMe, 1-n-butyloxyethyl, CH2CH2), (A720, Cl, Cl, OMe, 1-n-butyloxypropyl, CH2CH2), (A721, Cl, Cl, OMe, 1-n-butyloxybutyl, CH2CH2), (A722, Cl, Cl, OMe, 1-n-butyloxy-2-methylpropyl, CH2CH2), (A723, Cl, Cl, OMe, 1-n-butyloxypentyl, CH2CH2), (A724, Cl, Cl, OMe, 1-n-butyloxy-3-methylbutyl, CH2CH2), (A725, Cl, Cl, OMe, 1-n-butyloxy-2,2-dimethylpropyl, CH2CH2), (A726, Cl, Cl, OMe, 1-n-butyloxyhexyl, CH2CH2), (A727, Cl, Cl, OMe, 1-n-butyloxy-3,3-dimethylbutyl, CH2CH2), (A728, Cl, Cl, OMe, 1-isobutyloxyethyl, CH2CH2), (A729, Cl, Cl, OMe, 1-isobutyloxypropyl, CH2CH2), (A730, Cl, Cl, OMe, 1-isobutyloxybutyl, CH2CH2), (A731, Cl, Cl, OMe, 1-isobutyloxy-2-methylpropyl, CH2CH2), (A732, Cl, Cl, OMe, 1-isobutyloxypentyl, CH2CH2), (A733, Cl, Cl, OMe, 1-isobutyloxy-3-methylbutyl, CH2CH2), (A734, Cl, Cl, OMe, 1-isobutyloxy-2,2-dimethylpropyl, CH2CH2), (A735, Cl, Cl, OMe, 1-isobutyloxyhexyl, CH2CH2), (A736, Cl, Cl, OMe, 1-isobutyloxy-3,3-dimethylbutyl, CH2CH2), (A737, Cl, Cl, OMe, 1-t-butyloxyethyl, CH2CH2), (A738; Cl, Cl, OMe, 1-t-butyloxypropyl, CH2CH2), (A739, Cl, Cl, OMe, 1-t-butyloxybutyl, CH2CH2), (A740, Cl, Cl, OMe, 1-t-butyloxy-2-methylpropyl, CH2CH2), (A741, Cl, Cl, OMe, 1-t-butyloxypentyl, CH2CH2), (A742, Cl, Cl, OMe, 1-t-butyloxy-3-methylbutyl, CH2CH2), (A743, Cl, Cl, OMe, 1-t-butyloxy-2,2-dimethylpropyl, CH2CH2), (A744, Cl, Cl, OMe, 1-t-butyloxyhexyl, CH2CH2), (A745, Cl, Cl, OMe, 1-t-butyloxy-3,3-dimethylbutyl, CH2CH2), (A746, Cl, Cl, OMe, 1-n-pentyloxyethyl, CH2CH2), (A747, Cl, Cl, OMe, 1-n-pentyloxypropyl, CH2CH2), (A748, Cl, Cl, OMe, 1-n-pentyloxybutyl, CH2CH2), (A749, Cl, Cl, OMe, 1-n-pentyloxy-2-methylpropyl, CH2CH2), (A750, Cl, Cl, OMe, 1-n-pentyloxypentyl, CH2CH2), (A751, Cl, Cl, OMe, 1-n-pentyloxy-3-methylbutyl, CH2CH2), (A752, Cl, Cl, OMe, 1-n-pentyloxy-2,2-dimethylpropyl, CH2CH2), (A753, Cl, Cl, OMe, 1-n-pentyloxyhexyl, CH2CH2), (A754, Cl, Cl, OMe, 1-n-pentyloxy-3,3-dimethylbutyl, CH2CH2), (A755, Cl, Cl, OMe, 1-neopentyloxyethyl, CH2CH2), (A756, Cl, Cl, OMe, 1-neopentyloxypropyl, CH2CH2), (A757, Cl, Cl, OMe, 1-neopentyloxybutyl, CH2CH2), (A758, Cl, Cl, OMe, 1-neopentyloxy-2-methylpropyl, CH2CH2), (A759, Cl, Cl, OMe, 1-neopentyloxypentyl, CH2CH2), (A760, Cl, Cl, OMe, 1-neopentyloxy-3-methylbutyl, CH2CH2), (A761, Cl, Cl, OMe, 1-neopentyloxy-2,2-dimethylpropyl, CH2CH2), (A762, Cl, Cl, OMe, 1-neopentyloxyhexyl, CH2CH2), (A763, Cl, Cl, OMe, 1-neopentyloxy-3,3-dimethylbutyl, CH2CH2), (A764, Cl, Cl, Me, 1-methyloxyethyl, OCH2), (A765, Cl, Cl, Me, 1-methyloxypropyl, OCH2), (A766, Cl, Cl, Me, 1-methyloxybutyl, OCH2), (A767, Cl, Cl, Me, 1-methyloxy-2-methylpropyl, OCH2), (A768, Cl, Cl, Me, 1-methyloxypentyl, OCH2), (A769, Cl, Cl, Me, 1-methyloxy-3-methylbutyl, OCH2), (A770, Cl, Cl, Me, 1-methyloxy-2,2-dimethylpropyl, OCH2), (A771, Cl, Cl, Me, 1-methyloxyhexyl, OCH2), (A772, Cl, Cl, Me, 1-methyloxy-3,3-dimethylbutyl, OCH2), (A773, Cl, Cl, Me, 1-ethyloxyethyl, OCH2), (A774, Cl, Cl, Me, 1-ethyloxypropyl, OCH2), (A775, Cl, Cl, Me, 1-ethyloxybutyl, OCH2), (A776, Cl, Cl, Me, 1-ethyloxy-2-methylpropyl, OCH2), (A777, Cl, Cl, Me, 1-ethyloxypentyl, OCH2), (A778, Cl, Cl, Me, 1-ethyloxy-3-methylbutyl, OCH2), (A779, Cl, Cl, Me, 1-ethyloxy-2,2-dimethylpropyl, OCH2), (A780, Cl, Cl, Me, 1-ethyloxyhexyl, OCH2), (A781, Cl, Cl, Me, 1-ethyloxy-3,3-dimethylbutyl, OCH2), (A782, Cl, Cl, Me, 1-n-propyloxyethyl, OCH2), (A783, Cl, Cl, Me, 1-n-propyloxypropyl, OCH2), (A784, Cl, Cl, Me, 1-n-propyloxybutyl, OCH2), (A785, Cl, Cl, Me, 1-n-propyloxy-2-methylpropyl, OCH2), (A786, Cl, Cl, Me, 1-n-propyloxypentyl, OCH2), (A787, Cl, Cl, Me, 1-n-propyloxy-3-methylbutyl, OCH2), (A788, Cl, Cl, Me, 1-n-propyloxy-2,2-dimethylpropyl, OCH2), (A789, Cl, Cl, Me, 1-n-propyloxyhexyl, OCH2), (A790, Cl, Cl, Me, 1-n-propyloxy-3,3-dimethylbutyl, OCH2), (A791, Cl, Cl, Me, 1-isopropyloxyethyl, OCH2), (A792, Cl, Cl, Me, 1-isopropyloxypropyl, OCH2), (A793, Cl, Cl, Me, 1-isopropyloxybutyl, OCH2), (A794, Cl, Cl, Me, 1-isopropyloxy-2-methylpropyl, OCH2), (A795, Cl, Cl, Me, 1-isopropyloxypentyl, OCH2), (A796, Cl, Cl, Me, 1-isopropyloxy-3-methylbutyl, OCH2), (A797, Cl, Cl, Me, 1-isopropyloxy-2,2-dimethylpropyl, OCH2), (A798, Cl, Cl, Me, 1-isopropyloxyhexyl, OCH2), (A799, Cl, Cl, Me, 1-isopropyloxy-3,3-dimethylbutyl, OCH2), (A800, Cl, Cl, Me, 1-n-butyloxyethyl, OCH2), (A801, Cl, Cl, Me, 1-n-butyloxypropyl, OCH2), (A802, Cl, Cl, Me, 1-n-butyloxybutyl, OCH2), (A803, Cl, Cl, Me, 1-n-butyloxy-2-methylpropyl, OCH2), (A804, Cl, Cl, Me, 1-n-butyloxypentyl, OCH2), (A805, Cl, Cl, Me, 1-n-butyloxy-3-methylbutyl, OCH2), (A806, Cl, Cl, Me, 1-n-butyloxy-2,2-dimethylpropyl, OCH2), (A807, Cl, Cl, Me, 1-n-butyloxyhexyl, OCH2), (A808, Cl, Cl, Me, 1-n-butyloxy-3,3-dimethylbutyl, OCH2), (A809, Cl, Cl, Me, 1-isobutyloxyethyl, OCH2), (A810, Cl, Cl, Me, 1-isobutyloxypropyl, OCH2), (A811, Cl, Cl, Me, 1-isobutyloxybutyl, OCH2), (A812, Cl, Cl, Me, 1-isobutyloxy-2-methylpropyl, OCH2), (A813, Cl, Cl, Me, 1-isobutyloxypentyl, OCH2), (A814, Cl, Cl, Me, 1-isobutyloxy-3-methylbutyl, OCH2), (A815, Cl, Cl, Me, 1-isobutyloxy-2,2-dimethylpropyl, OCH2), (A816, Cl, Cl, Me, 1-isobutyloxyhexyl, OCH2), (A817, Cl, Cl, Me, 1-isobutyloxy-3,3-dimethylbutyl, OCH2), (A818, Cl, Cl, Me, 1-t-butyloxyethyl, OCH2), (A819, Cl, Cl, Me, 1-t-butyloxypropyl, OCH2), (A820, Cl, Cl, Me, 1-t-butyloxybutyl, OCH2), (A821, Cl, Cl, Me, 1-t-butyloxy-2-methylpropyl, OCH2), (A822, Cl, Cl, Me, 1-t-butyloxypentyl, OCH2), (A823, Cl, Cl, Me, 1-t-butyloxy-3-methylbutyl, OCH2), (A824, Cl, Cl, Me, 1-t-butyloxy-2,2-dimethylpropyl, OCH2), (A825, Cl, Cl, Me, 1-t-butyloxyhexyl, OCH2), (A826, Cl, Cl, Me, 1-t-butyloxy-3,3-dimethylbutyl, OCH2), (A827, Cl, Cl, Me, 1-n-pentyloxyethyl, OCH2), (A828, Cl, Cl, Me, 1-n-pentyloxypropyl, OCH2), (A829, Cl, Cl, Me, 1-n-pentyloxybutyl, OCH2), (A830, Cl, Cl, Me, 1-n-pentyloxy-2-methylpropyl, OCH2), (A831, Cl, Cl, Me, 1-n-pentyloxypentyl, OCH2), (A832, Cl, Cl, Me, 1-n-pentyloxy-3-methylbutyl, OCH2), (A833, Cl, Cl, Me, 1-n-pentyloxy-2,2-dimethylpropyl, OCH2), (A834, Cl, Cl, Me, 1-n-pentyloxyhexyl, OCH2), (A835, Cl, Cl, Me, 1-n-pentyloxy-3,3-dimethylbutyl, OCH2), (A836, Cl, Cl, Me, 1-neopentyloxyethyl, OCH2), (A837, Cl, Cl, Me, 1-neopentyloxypropyl, OCH2), (A838, Cl, Cl, Me, 1-neopentyloxybutyl, OCH2), (A839, Cl, Cl, Me, 1-neopentyloxy-2-methylpropyl, OCH2), (A840, Cl, Cl, Me, 1-neopentyloxypentyl, OCH2), (A841, Cl, Cl, Me, 1-neopentyloxy-3-methylbutyl, OCH2), (A842, Cl, Cl, Me, 1-neopentyloxy-2,2-dimethylpropyl, OCH2), (A843, Cl, Cl, Me, 1-neopentyloxyhexyl, OCH2), (A844, Cl, Cl, Me, 1-neopentyloxy-3,3-dimethylbutyl, OCH2), (A845, Cl, Cl, OMe, 1-methyloxyethyl, OCH2), (A846, Cl, Cl, OMe, 1-methyloxypropyl, OCH2), (A847, Cl, Cl, OMe, 1-methyloxybutyl, OCH2), (A848, Cl, Cl, OMe, 1-methyloxy-2-methylpropyl, OCH2), (A849, Cl, Cl, OMe, 1-methyloxypentyl, OCH2), (A850, Cl, Cl, OMe, 1-methyloxy-3-methylbutyl, OCH2), (A851, Cl, Cl, OMe, 1-methyloxy-2,2-dimethylpropyl, OCH2), (A852, Cl, Cl, OMe, 1-methyloxyhexyl, OCH2), (A853, Cl, Cl, OMe, 1-methyloxy-3,3-dimethylbutyl, OCH2), (A854, Cl, Cl, OMe, 1-ethyloxyethyl, OCH2), (A855, Cl, Cl, OMe, 1-ethyloxypropyl, OCH2), (A856, Cl, Cl, OMe, 1-ethyloxybutyl, OCH2), (A857, Cl, Cl, OMe, 1-ethyloxy-2-methylpropyl, OCH2), (A858, Cl, Cl, OMe, 1-ethyloxypentyl, OCH2), (A859, Cl, Cl, OMe, 1-ethyloxy-3-methylbutyl, OCH2), (A860, Cl, Cl, OMe, 1-ethyloxy-2,2-dimethylpropyl, OCH2), (A861, Cl, Cl, OMe, 1-ethyloxyhexyl, OCH2), (A862, Cl, Cl, OMe, 1-ethyloxy-3,3-dimethylbutyl, OCH2), (A863, Cl, Cl, OMe, 1-n-propyloxyethyl, OCH2), (A864, Cl, Cl, OMe, 1-n-propyloxypropyl, OCH2), (A865, Cl, Cl, OMe, 1-n-propyloxybutyl, OCH2), (A866, Cl, Cl, OMe, 1-n-propyloxy-2-methylpropyl, OCH2), (A867, Cl, Cl, OMe, 1-n-propyloxypentyl, OCH2), (A868, Cl, Cl, OMe, 1-n-propyloxy-3-methylbutyl, OCH2), (A869, Cl, Cl, OMe, 1-n-propyloxy-2,2-dimethylpropyl, OCH2), (A870, Cl, Cl, OMe, 1-n-propyloxyhexyl, OCH2), (A871, Cl, Cl, OMe, 1-n-propyloxy-3,3-dimethylbutyl, OCH2), (A872, Cl, Cl, OMe, 1-isopropyloxyethyl, OCH2), (A873, Cl, Cl, OMe, 1-isopropyloxypropyl, OCH2), (A874, Cl, Cl, OMe, 1-isopropyloxybutyl, OCH2), (A875, Cl, Cl, OMe, 1-isopropyloxy-2-methylpropyl, OCH2), (A876, Cl, Cl, OMe, 1-isopropyloxypentyl, OCH2), (A877, Cl, Cl, OMe, 1-isopropyloxy-3-methylbutyl, OCH2), (A878, Cl, Cl, OMe, 1-isopropyloxy-2,2-dimethylpropyl, OCH2), (A879, Cl, Cl, OMe, 1-isopropyloxyhexyl, OCH2), (A880, Cl, Cl, OMe, 1-isopropyloxy-3,3-dimethylbutyl, OCH2), (A881, Cl, Cl, OMe, 1-n-butyloxyethyl, OCH2), (A882, Cl, Cl, OMe, 1-n-butyloxypropyl, OCH2), (A883, Cl, Cl, OMe, 1-n-butyloxybutyl, OCH2), (A884, Cl, Cl, OMe, 1-n-butyloxy-2-methylpropyl, OCH2), (A885, Cl, Cl, OMe, 1-n-butyloxypentyl, OCH2), (A886, Cl, Cl, OMe, 1-n-butyloxy-3-methylbutyl, OCH2), (A887, Cl, Cl, OMe, 1-n-butyloxy-2,2-dimethylpropyl, OCH2), (A888, Cl, Cl, OMe, 1-n-butyloxyhexyl, OCH2), (A889, Cl, Cl, OMe, 1-n-butyloxy-3,3-dimethylbutyl, OCH2), (A890, Cl, Cl, OMe, 1-isobutyloxyethyl, OCH2), (A891, Cl, Cl, OMe, 1-isobutyloxypropyl, OCH2), (A892, Cl, Cl, OMe, 1-isobutyloxybutyl, OCH2), (A893, Cl, Cl, OMe, 1-isobutyloxy-2-methylpropyl, OCH2), (A894, Cl, Cl, OMe, 1-isobutyloxypentyl, OCH2), (A895, Cl, Cl, OMe, 1-isobutyloxy-3-methylbutyl, OCH2), (A896, Cl, Cl, OMe, 1-isobutyloxy-2,2-dimethylpropyl, OCH2), (A897, Cl, Cl, OMe, 1-isobutyloxyhexyl, OCH2), (A898, Cl, Cl, OMe, 1-isobutyloxy-3,3-dimethylbutyl, OCH2), (A899, Cl, C1, OMe, .1-t-butyloxyethyl, OCH2), (A900, Cl, Cl, OMe, 1-t-butyloxypropyl, OCH2), (A901, Cl, Cl, OMe, 1-t-butyloxybutyl, OCH2), (A902, Cl, Cl, OMe, 1-t-butyloxy-2-methylpropyl, OCH2), (A903, Cl, Cl, OMe, 1-t-butyloxypentyl, OCH2), (A904, Cl, Cl, OMe, 1-t-butyloxy-3-methylbutyl, OCH2), (A905, Cl, Cl, OMe, 1-t-butyloxy-2,2-dimethylpropyl, OCH2), (A906, Cl, Cl, OMe, 1-t-butyloxyhexyl, OCH2), (A907, Cl, C1, OMe, 1-t-butyloxy-3,3-dimethylbutyl, OCH2), (A908, Cl, Cl, OMe, 1-n-pentyloxyethyl, OCH2), (A909, Cl, Cl, OMe, 1-n-pentyloxypropyl, OCH2), (A910, Cl, Cl, OMe, 1-n-pentyloxybutyl, OCH2), (A911, Cl, Cl, OMe, 1-n-pentyloxy-2-methylpropyl, OCH2), (A912, Cl, Cl, OMe, 1-n-pentyloxypentyl, OCH2), (A913, Cl, Cl, OMe, 1-n-pentyloxy-3-methylbutyl, OCH2), (A914, Cl, Cl, OMe, 1-n-pentyloxy-2,2-dimethylpropyl, OCH2), (A915, Cl, Cl, OMe, 1-n-pentyloxyhexyl, OCH2), (A916, Cl, Cl, OMe, 1-n-pentyloxy-3,3-dimethylbutyl, OCH2), (A917, Cl, Cl, OMe, 1-neopentyloxyethyl, OCH2), (A918, Cl, Cl, OMe, 1-neopentyloxypropyl, OCH2), (A919, Cl, Cl, OMe, 1-neopentyloxybutyl, OCH2), (A920, Cl, Cl, OMe, 1-neopentyloxy-2-methylpropyl, OCH2), (A921, Cl, Cl, OMe, 1-neopentyloxypentyl, OCH2), (A922, Cl, Cl, OMe, 1-neopentyloxy-3-methylbutyl, OCH2), (A923, Cl, Cl, OMe, 1-neopentyloxy-2,2-dimethylpropyl, OCH2), (A924, Cl, Cl, OMe, 1-neopentyloxyhexyl, OCH2), (A925, Cl, Cl, OMe, 1-neopentyloxy-3,3-dimethylbutyl, OCH2), (A926, Cl, Cl, Me, 3-methyloxypropyl, CH2CH2), (A927, Cl, Cl, Me, 3-methyloxybutyl, CH2CH2), (A929, Cl, Cl, Me, 3-methyloxy-4-methylpentyl, CH2CH2), (A931, Cl, Cl, Me, 3-methyloxy-5-methylhexyl, CH2CH2), (A933, Cl, Cl, Me, 3-methyloxyoctyl, CH2CH2), (A934, Cl, Cl, Me, 3-methyloxy-5,5-dimethylhexyl, CH2CH2), (A935, Cl, Cl, Me, 3-ethyloxybutyl, CH2CH2), (A938, Cl, Cl, Me, 3-ethyloxy-4-methylpentyl, CH2CH2), (A940, Cl, Cl, Me, 3-ethyloxy-5-methylhexyl, CH2CH2), (A942, Cl, Cl, Me, 3-ethyloxyoctyl, CH2CH2), (A943, Cl, Cl, Me, 3-ethyloxy-5,5-dimethylhexyl, CH2CH2), (A945, Cl, Cl, Me, 3-n-propyloxybutyl, CH2CH2), (A946, Cl, Cl, Me, 3-n-propyloxypentyl, CH2CH2), (A947, Cl, Cl, Me, 3-n-propyloxyhexyl, CH2CH2), (A948, Cl, Cl, Me, 3-n-propyloxy-4-methylpentyl, CH2CH2), (A949, Cl, Cl, Me, 3-n-propyloxyheptyl, CH2CH2), (A950, Cl, Cl, Me, 3-n-propyloxy-5-methylhexyl, CH2CH2), (A951, Cl, Cl, Me, 3-n-propyloxy-4,4-dimethylpentyl, CH2CH2), (A952, Cl, Cl, Me, 3-n-propyloxyoctyl, CH2CH2), (A953, Cl, Cl, Me, 3-n-propyloxy-5,5-dimethylhexyl, CH2CH2), (A955, Cl, Cl, Me, 3-isopropyloxybutyl, CH2CH2), (A956, Cl, Cl, Me, 3-isopropyloxypentyl, CH2CH2), (A957, Cl, Cl, Me, 3-isopropyloxyhexyl, CH2CH2), (A958, Cl, Cl, Me, 3-isopropyloxy-4-methylpentyl, CH2CH2), (A959, Cl, Cl, Me, 3-isopropyloxyheptyl, CH2CH2), (A960, Cl, Cl, Me, 3-isopropyloxy-5-methylhexyl, CH2CH2), (A961, Cl, Cl, Me, 3-isopropyloxy-4,4-dimethylpentyl, CH2CH2), (A962, Cl, Cl, Me, ³-isopropyloxyoctyl, CH2CH2), (A963, Cl, Cl, Me, 3-isopropyloxy-5,5-dimethylhexyl, CH2CH2), (A964, Cl, Cl, Me, 3-n-butyloxybutyl, CH2CH2), (A965, Cl, Cl, Me, 3-n-butyloxypentyl, CH2CH2), (A966, Cl, Cl, Me, 3-n-butyloxyhexyl, CH2CH2), (A967, Cl, Cl, Me, 3-n-butyloxy-4-methylpentyl, CH2CH2), (A968, Cl, Cl, Me, 3-n-butyloxyheptyl, CH2CH2), (A969, Cl, Cl, Me, 3-n-butyloxy-5-methylhexyl, CH2CH2), (A970, Cl, Cl, Me, 3-n-butyloxy-4,4-dimethylpentyl, CH2CH2), (A971, Cl, Cl, Me, 3-n-butyloxyoctyl, CH2CH2), (A972, Cl, Cl, Me, 3-n-butyloxy-5,5-dimethylhexyl, CH2CH2), (A973, Cl, Cl, Me, 3-isobutyloxypropyl, CH2CH2), (A974, Cl, Cl, Me, 3-isobutyloxybutyl, CH2CH2), (A975, Cl, Cl, Me, 3-isobutyloxypentyl, CH2CH2), (A976, Cl, Cl, Me, 3-isobutyloxyhexyl, CH2CH2), (A977, Cl, Cl, Me, 3-isobutyloxy-4-methylpentyl, CH2CH2), (A978, Cl, Cl, Me, 3-isobutyloxyheptyl, CH2CH2), (A979, Cl, Cl, Me, 3-isobutyloxy-5-methylhexyl, CH2CH2), (A980, Cl, Cl, Me, 3-isobutyloxy-4,4-dimethylpentyl, CH2CH2), (A981, Cl, Cl, Me, 3-isobutyloxyoctyl, CH2CH2), (A982, Cl, Cl, Me, 3-isobutyloxy-5,5-dimethylhexyl, CH2CH2), (A983, Cl, Cl, Me, 3-t-butyloxypropyl, CH2CH2), (A984, Cl, Cl, Me, 3-t-butyloxybutyl, CH2CH2), (A985, Cl, Cl, Me, 3-t-butyloxypentyl, CH2CH2), (A986, Cl, Cl, Me, 3-t-butyloxyhexyl, CH2CH2), (A987, Cl, Cl, Me, 3-t-butyloxy-4-methylpentyl, CH2CH2), (A988, Cl, Cl, Me, 3-t-butyloxyheptyl, CH2CH2), (A989, Cl, Cl, Me, 3-t-butyloxy-5-methylhexyl, CH2CH2), (A990, Cl, Cl, Me, 3-t-butyloxy-4,4-dimethylpentyl, CH2CH2), (A991, Cl, Cl, Me, 3-t-butyloxyoctyl, CH2CH2), (A992, Cl, Cl, Me, 3-t-butyloxy-5,5-dimethylhexyl, CH2CH2), (A994, Cl, Cl, Me, 3-n-pentyloxybutyl, CH2CH2), (A995, Cl, Cl, Me, 3-n-pentyloxypentyl, CH2CH2), (A996, Cl, Cl, Me, 3-n-pentyloxyhexyl, CH2CH2), (A997, Cl, Cl, Me, 3-n-pentyloxy-4-methylpentyl, CH2CH2), (A998, Cl, Cl; Me, 3-n-pentyloxyheptyl, CH2CH2), (A999, Cl, Cl, Me, 3-n-pentyloxy-5-methylhexyl, CH2CH2), (A1000, Cl, Cl, Me, 3-n-pentyloxy-4,4-dimethylpentyl, CH2CH2), (A1001, Cl, Cl, Me, 3-n-pentyloxyoctyl, CH2CH2), (A1002, Cl, Cl, Me, 3-n-pentyloxy-5,5-dimethylhexyl, CH2CH2), (A1004, Cl, Cl, Me, 3-neopentyloxybutyl, CH2CH2), (A1005, Cl, Cl, Me, 3-neopentyloxypentyl, CH2CH2), (A1006, Cl, Cl, Me, 3-neopentyloxyhexyl, CH2CH2), (A1007, Cl, Cl, Me, 3-neopentyloxy-4-methylpentyl, CH2CH2), (A1008, Cl, Cl, Me, 3-neopentyloxyheptyl, CH2CH2), (A1009, Cl, Cl, Me, 3-neopentyloxy-5-methylhexyl, CH2CH2), (A1010, Cl, Cl, Me, 3-neopentyloxy-4,4-dimethylpentyl, CH2CH2), (A1011, Cl, Cl, Me, 3-neopentyloxyoctyl, CH2CH2), (A1012, C1, Cl, Me, 3-neopentyloxy-5,5-dimethylhexyl, CH2CH2), (A1013, Cl, Cl, OMe, 3-methyloxypropyl, CH2CH2), (A1014, Cl, Cl, OMe, 3-methyloxybutyl, CH2CH2), (A10I5, Cl, Cl, OMe, 3-methyloxypentyl, CH2CH2), (A1017, Cl, Cl, OMe, 3-methyloxy-4-methylpentyl, CH2CH2), (A1019, Cl, Cl, OMe, 3-methyloxy-5-methylhexyl, CH2CH2), (A1020, Cl, Cl, OMe, 3-metoxy-4,4-dimethylpentyl, CH2CH2), (A1021, Cl, Cl, OMe, 3-methyloxyoctyl, CH2CH2), (A1022, Cl, Cl, OMe, 3-methyloxy-5,5-dimethylhexyl, CH2CH2), (A1023, Cl, Cl, OMe, 3-ethyloxypropyl, CH2CH2), (A1024, Cl, Cl, OMe, 3-ethyloxybutyl, CH2CH2), (A1025, Cl, Cl, OMe, 3-ethyloxypentyl, CH2CH2), (A1026, Cl, Cl, OMe, 3-ethyloxyhexyl, CH2CH2), (A1027, Cl, Cl, OMe, 3-ethyloxy-4-methylpentyl, CH2CH2), (A1028, Cl, Cl, OMe, 3-ethyloxyheptyl, CH2CH2), (A1029, Cl, Cl, OMe, 3-ethyloxy-5-methylhexyl, CH2CH2), (A1030, C1, Cl, OMe, 3-etoxy-4,4-dimethylpentyl, CH2CH2), (A1031, Cl, Cl, OMe, 3-ethyloxyoctyl, CH2CH2), (A1032, Cl, Cl, OMe, 3-ethyloxy-5,5-dimethylhexyl, CH2CH2), (A1034, Cl, Cl, OMe, 3-n-propyloxybutyl, CH2CH2), (A1035, Cl, Cl, OMe, 3-n-propyloxypentyl, CH2CH2), (A1036, Cl, Cl, OMe, 3-n-propyloxyhexyl, CH2CH2), (A1037, Cl, Cl, OMe, 3-n-propyloxy-4-methylpentyl, CH2CH2), (A1038, Cl, Cl, OMe, 3-n-propyloxyheptyl, CH2CH2), (A1039, Cl, Cl, OMe, 3-n-propyloxy-5-methylhexyl, CH2CH2), (A1040, Cl, Cl, OMe, 3-n-propyloxy-4,4-dimethylpentyl, CH2CH2), (A1041, Cl, Cl, OMe, 3-n-propyloxyoctyl, CH2CH2), (A1042, Cl, Cl, OMe, 3-n-propyloxy-5,5-dimethylhexyl, CH2CH2), (A1043, Cl, Cl, OMe, 3-isopropyloxypropyl, CH2CH2), (A1044, Cl, Cl, OMe, 3-isopropyloxybutyl, CH2CH2), (A1045, Cl, Cl, OMe, 3-isopropyloxypentyl, CH2CH2), (A1046, Cl, Cl, OMe, 3-isopropyloxyhexyl, CH2CH2), (A1047, Cl, Cl, OMe, 3-isopropyloxy-4-methylpentyl, CH2CH2), (A1048, Cl, Cl, OMe, 3-isopropyloxyheptyl, CH2CH2), (A1049, Cl, Cl, OMe, 3-isopropyloxy-5-methylhexyl, CH2CH2), (A1050, Cl, Cl, OMe, 3-isopropyloxy-4,4-dimethylpentyl, CH2CH2), (A1051, Cl, Cl, OMe, 3-isopropyloxyoctyl, CH2CH2), (A1052, Cl, Cl, OMe, 3-isopropyloxy-5,5-dimethylhexyl, CH2CH2), (A1053, Cl, Cl, OMe, 3-n-butyloxypropyl, CH2CH2), (A1054, Cl, Cl, OMe, 3-n-butyloxybutyl, CH2CH2), (A1055, Cl, Cl, OMe, 3-n-butyloxypentyl, CH2CH2), (A1056, Cl, Cl, OMe, 3-n-butyloxyhexyl, CH2CH2), (A1057, Cl, Cl, OMe, 3-n-butyloxy-4-methylpentyl, CH2CH2), (A1058, Cl, Cl, OMe, 3-n-butyloxyheptyl, CH2CH2), (A1059, Cl, Cl, OMe, 3-n-butyloxy-5-methylhexyl, CH2CH2), (A1060, Cl, Cl, OMe, 3-n-butyloxy-4,4-dimethylpentyl, CH2CH2), (A1061, Cl, Cl, OMe, 3-n-butyloxyoctyl, CH2CH2), (A1062, Cl, Cl, OMe, 3-n-butyloxy-5,5-dimethylhexyl, CH2CH2), (A1063, Cl, Cl, OMe, 3-isobutyloxypropyl, CH2CH2), (A1064, Cl, Cl, OMe, 3-isobutyloxybutyl, CH2CH2), (A1065, Cl, Cl, OMe, 3-isobutyloxypentyl, CH2CH2), (A1066, Cl, Cl, OMe, 3-isobutyloxyhexyl, CH2CH2), (A1067, Cl, Cl, OMe, 3-isobutyloxy-4-methylpentyl, CH2CH2), (A1068, Cl, Cl, OMe, 3-isobutyloxyheptyl, CH2CH2), (A1069, Cl, Cl, OMe, 3-isobutyloxy-5-methylhexyl, CH2CH2), (A1070, Cl, Cl, OMe, 3-isobutyloxy-4,4-dimethylpentyl, CH2CH2), (A1071, Cl, Cl, OMe, 3-isobutyloxyoctyl, CH2CH2), (A1072, Cl, Cl, OMe, 3-isobutyloxy-5,5-dimethylhexyl, CH2CH2), (A1073, Cl, Cl, OMe, 3-t-butyloxypropyl, CH2CH2), (A1074, Cl, Cl, OMe, 3-t-butyloxybutyl, CH2CH2), (A1075, Cl, Cl, OMe, 3-t-butyloxypentyl, CH2CH2), (A1076, Cl, Cl, OMe, 3-t-butyloxyhexyl, CH2CH2), (A1077, Cl, Cl, OMe, 3-t-butyloxy-4-methylpentyl, CH2CH2), (A1078, Cl, Cl, OMe, 3-t-butyloxyheptyl, CH2CH2), (A1079, Cl, Cl, OMe, 3-t-butyloxy-5-methylhexyl, CH2CH2), (A1080, Cl, Cl, OMe, 3-t-butyloxy-4,4-dimethylpentyl, CH2CH2), (A1081, Cl, Cl, OMe, 3-t-butyloxyoctyl, CH2CH2), (A1082, Cl, Cl, OMe, 3-t-butyloxy-5,5-dimethylhexyl, CH2CH2), (A1083, Cl, Cl, OMe, 3-n-pentyloxypropyl, CH2CH2), (A1084, Cl, Cl, OMe, 3-n-pentyloxybutyl, CH2CH2), (A1085, Cl, Cl, OMe, 3-n-pentyloxypentyl, CH2CH2), (A1086, Cl, Cl, OMe, 3-n-pentyloxyhexyl, CH2CH2), (A1087, Cl, Cl, OMe, 3-n-pentyloxy-4-methylpentyl, CH2CH2), (A1088, Cl, Cl, OMe, 3-n-pentyloxyheptyl, CH2CH2), (A1089, Cl, Cl, OMe, 3-n-pentyloxy-5-methylhexyl, CH2CH2), (A1090, Cl, Cl, OMe, 3-n-pentyloxy-4,4-dimethylpentyl, CH2CH2), (A1091, Cl, Cl, OMe, 3-n-pentyloxyoctyl, CH2CH2), (A1092, Cl, Cl, OMe, 3-n-pentyloxy-5,5-dimethylhexyl, CH2CH2), (A1093, Cl, Cl, OMe, 3-neopentyloxypropyl, CH2CH2), (A1094, Cl, Cl, OMe, 3-neopentyloxybutyl, CH2CH2), (A1095, Cl, Cl, OMe, 3-neopentyloxypentyl, CH2CH2), (A1096, Cl, Cl, OMe, 3-neopentyloxyhexyl, CH2CH2), (A1097, Cl, Cl, OMe, 3-neopentyloxy-4-methylpentyl, CH2CH2), (A1098, Cl, Cl, OMe, 3-neopentyloxyheptyl, CH2CH2), (A1099, Cl, Cl, OMe, 3-neopentyloxy-5-methylhexyl, CH2CH2), (A1100, Cl, Cl, OMe, 3-neopentyloxy-4,4-dimethylpentyl, CH2CH2), (A1101, Cl, Cl, OMe, 3-neopentyloxyoctyl, CH2CH2), (A1102, Cl, Cl, OMe, 3-neopentyloxy-5,5-dimethylhexyl, CH2CH2), (A1103, Cl, Cl, Me, 3-methyloxypropyl, OCH2), (A1104, Cl, Cl, Me, 3-methyloxybutyl, OCH2), (A1105, Cl, Cl, Me, 3-methyloxypentyl, OCH2), (A1106, Cl, Cl, Me, 3-methyloxyhexyl, OCH2), (A1107, Cl, Cl, Me, 3-methyloxy-4-methylpentyl, OCH2), (A1108, Cl, Cl, Me, 3-methyloxyheptyl, OCH2), (A1109, Cl, Cl, Me, 3-methyloxy-5-methylhexyl, OCH2), (A1110, Cl, Cl, Me, 3-metoxy-4,4-dimethylpentyl, OCH2), (A1111, Cl, Cl, Me, 3-methyloxyoctyl, OCH2), (A1112, Cl, Cl, Me, 3-methyloxy-5,5-dimethylhexyl, OCH2), (A1113, Cl, Cl, Me, 3-ethyloxypropyl, OCH2), (A1114, Cl, Cl, Me, 3-ethyloxybutyl, OCH2), (Ai115, Cl, Cl, Me, 3-ethyloxypentyl, OCH2), (A1116, Cl, Cl, Me, 3-ethyloxyhexyl, OCH2), (A1117, Cl, Cl, Me, 3-ethyloxy-4-methylpentyl, OCH2), (A1118, Cl, Cl, Me, 3-ethyloxyheptyl, OCH2), (A1119, Cl, Cl, Me, 3-ethyloxy-5-methylhexyl, OCH2), (A1120, Cl, Cl, Me, 3-etoxy-4,4-dimethylpentyl, OCH2), (A1121, Cl, Cl, Me, 3-ethyloxyoctyl, OCH2), (A1122, Cl, Cl, Me, 3-ethyloxy-5,5-dimethylhexyl, OCH2), (A1124, Cl, Cl, Me, 3-n-propyloxybutyl, OCH2), (A1125, Cl, Cl, Me, 3-n-propyloxypentyl, OCH2), (A1126, Cl, Cl, Me, 3-n-propyloxyhexyl, OCH2), (A1127, Cl, Cl, Me, 3-n-propyloxy-4-methylpentyl, OCH2), (A1128, Cl, Cl, Me, 3-n-propyloxyheptyl, OCH2), (A1129, Cl, Cl, Me, 3-n-propyloxy-5-methylhexyl, OCH2), (A1130, Cl, Cl, Me, 3-n-propyloxy-4,4-dimethylpentyl, OCH2), (A1131, Cl, Cl, Me, 3-n-propyloxyoctyl, OCH2), (A1132, Cl, Cl, Me, 3-n-propyloxy-5,5-dimethylhexyl, OCH2), (A1133, Cl, Cl, Me, 3-isopropyloxypropyl, OCH2), (A1134, Cl, Cl, Me, 3-isopropyloxybutyl, OCH2), (A1135, Cl, Cl, Me, 3-isopropyloxypentyl, OCH2), (A1136, Cl, Cl, Me, 3-isopropyloxyhexyl, OCH2), (A1137, Cl, Cl, Me, 3-isopropyloxy-4-methylpentyl, OCH2), (A1138, Cl, Cl, Me, 3-isopropyloxyheptyl, OCH2), (A1139, Cl, Cl, Me, 3-isopropyloxy-5-methylhexyl, OCH2), (A1140, Cl, Cl, Me, 3-isopropyloxy-4,4-dimethylpentyl, OCH2), (A1141, Cl, Cl, Me, 3-isopropyloxyoctyl, OCH2), (A1142, Cl, Cl, Me, 3-isopropyloxy-5,5-dimethylhexyl, OCH2), (A1143, Cl, Cl, Me, 3-n-butyloxypropyl, OCH2), (A1144, Cl, Cl, Me, 3-n-butyloxybutyl, OCH2), (A1145, Cl, Cl, Me, 3-n-butyloxypentyl, OCH2), (A1146, Cl, Cl, Me, 3-n-butyloxyhexyl, OCH2), (A1147, Cl, Cl, Me, 3-n-butyloxy-4-methylpentyl, OCH2), (A1148, Cl, Cl, Me, 3-n-butyloxyheptyl, OCH2), (A1149, Cl, Cl, Me, 3-n-butyloxy-5-methylhexyl, OCH2), (A1150, Cl, Cl, Me, 3-n-butyloxy-4,4-dimethylpentyl, OCH2), (A1151, Cl, Cl, Me, 3-n-butyloxyoctyl, OCH2), (A1152, Cl, Cl, Me, 3-n-butyloxy-5,5-dimethylhexyl, OCH2), (A1153, Cl, Cl, Me, 3-isobutyloxypropyl, OCH2), (A1154, Cl, Cl, Me, 3-isobutyloxybutyl, OCH2), (A1155, Cl, Cl, Me, 3-isobutyloxypentyl, OCH2), (A1156, Cl, Cl, Me, 3-isobutyloxyhexyl, OCH2), (A1157, Cl, Cl, Me, 3-isobutyloxy-4-methylpentyl, OCH2), (A1158, Cl, Cl, Me, 3-isobutyloxyheptyl, OCH2), (A1159, Cl, Cl, Me, 3-isobutyloxy-5-methylhexyl, OCH2), (A1160, Cl, Cl, Me, 3-isobutyloxy-4,4-dimethylpentyl, OCH2), (A1161, Cl, Cl, Me, 3-isobutyloxyoctyl, OCH2), (A1162, Cl, Cl, Me, 3-isobutyloxy-5,5-dimethylhexyl, OCH2), (A1163, Cl, Cl, Me, 3-t-butyloxypropyl, OCH2), (A1164, Cl, Cl, Me, 3-t-butyloxybutyl, OCH2), (A1165, Cl, Cl, Me, 3-t-butyloxypentyl, OCH2), (A1166, Cl, Cl, Me, 3-t-butyloxyhexyl, OCH2), (A1167, Cl, Cl, Me, 3-t-butyloxy-4-methylpentyl, OCH2), (A1168, Cl, Cl, Me, 3-t-butyloxyheptyl, OCH2), (A1169, Cl, Cl, Me, 3-t-butyloxy-5-methylhexyl, OCH2), (A1170, Cl, Cl, Me, 3-t-butyloxy-4,4-dimethylpentyl, OCH2), (A1171, Cl, Cl, Me, 3-t-butyloxyoctyl, OCH2), (A1172, Cl, Cl, Me, 3-t-butyloxy-5,5-dimethylhexyl, OCH2), (A1173, Cl, Cl, Me, 3-n-pentyloxypropyl, OCH2), (A1174, Cl, Cl, Me, 3-n-pentyloxybutyl, OCH2), (A1175, Cl, Cl, Me, 3-n-pentyloxypentyl, OCH2), (A1176, Cl, Cl, Me, 3-n-pentyloxyhexyl, OCH2), (A1177, Cl, Cl, Me, 3-n-pentyloxy-4-methylpentyl, OCH2), (A1178, Cl, Cl, Me, 3-n-pentyloxyheptyl, OCH2), (A1179, Cl, Cl, Me, 3-n-pentyloxy-5-methylhexyl, OCH2), (A1180, Cl, Cl, Me, 3-n-pentyloxy-4,4-dimethylpentyl, OCH2), (A1181, Cl, Cl, Me, 3-n-pentyloxyoctyl, OCH2), (A1182, Cl, Cl, Me, 3-n-pentyloxy-5,5-dimethylhexyl, OCH2), (A1183, Cl, Cl, Me, 3-neopentyloxypropyl, OCH2), (A1184, Cl, Cl, Me, 3-neopentyloxybutyl, OCH2), (A1185, Cl, Cl, Me, 3-neopentyloxypentyl, OCH2), (A1186, C1, Cl, Me, 3-neopentyloxyhexyl, OCH2), (A1187, Cl, Cl, Me, 3-neopentyloxy-4-methylpentyl, OCH2), (A1188, Cl, Cl, Me, 3-neopentyloxyheptyl, OCH2), (A1189, Cl, Cl, Me, 3-neopentyloxy-5-methylhexyl, OCH2), (A1190, Cl, Cl, Me, 3-neopentyloxy-4,4-dimethylpentyl, OCH2), (A1191, Cl, Cl, Me, 3-neopentyloxyoctyl, OCH2), (A1192, Cl, Cl, Me, 3-neopentyloxy-5,5-dimethylhexyl, OCH2), (A1193, Cl, Cl, OMe, 3-methyloxypropyl, OCH2), (A1194, Cl, Cl, OMe, 3-methyloxybutyl, OCH2), (A1195, Cl, Cl, OMe, 3-methyloxypentyl, OCH2), (A1196, Cl, Cl, OMe, 3-methyloxyhexyl, OCH2), (A1197, Cl, Cl, OMe, 3-methyloxy-4-methylpentyl, OCH2), (A1198, Cl, Cl, OMe, 3-methyloxyheptyl, OCH2), (A1199, Cl, Cl, OMe, 3-methyloxy-5-methylhexyl, OCH2), (A1200, Cl, Cl, OMe, 3-metoxy-4,4-dimethylpentyl, OCH2), (A1201, Cl, Cl, OMe, 3-methyloxyoctyl, OCH2), (A1202, Cl, Cl, OMe, 3-methyloxy-5,5-dimethylhexyl, OCH2), (A1203, Cl, Cl, OMe, 3-ethyloxypropyl, OCH2), (A1204, Cl, Cl, OMe, 3-ethyloxybutyl, OCH2), (A1205, Cl, Cl, OMe, 3-ethyloxypentyl, OCH2), (A1206, Cl, Cl, OMe, 3-ethyloxyhexyl, OCH2), (A1207, Cl, Cl, OMe, 3-ethyloxy-4-methylpentyl, OCH2), (A1208, Cl, Cl, OMe, 3-ethyloxyheptyl, OCH2), (A1209, Cl, Cl, OMe, 3-ethyloxy-5-methylhexyl, OCH2), (A1210, Cl, Cl, OMe, 3-etoxy-4,4-dimethylpentyl, OCH2), (A1211, Cl, Cl, OMe, 3-ethyloxyoctyl, OCH2), (A1212, Cl, Cl, OMe, 3-ethyloxy-5,5-dimethylhexyl, OCH2), (A1213, Cl, Cl, OMe, 3-n-propyloxypropyl, OCH2), (A1214, Cl, Cl, OMe, 3-n-propyloxybutyl, OCH2), (A1215, Cl, Cl, OMe, 3-n-propyloxypentyl, OCH2), (A1216, Cl, Cl, OMe, 3-n-propyloxyhexyl, OCH2), (A1217, Cl, Cl, OMe, 3-n-propyloxy-4-methylpentyl, OCH2), (A1218, Cl, Cl, OMe, 3-n-propyloxyheptyl, OCH2), (A1219, Cl, Cl, OMe, 3-n-propyloxy-5-methylhexyl, OCH2), (A1220, Cl, Cl, OMe, 3-n-propyloxy-4,4-dimethylpentyl, OCH2), (A1221, Cl, Cl, OMe, 3-n-propyloxyoctyl, OCH2), (A1222, Cl, Cl, OMe, 3-n-propyloxy-5,5-dimethylhexyl, OCH2), (A1223, Cl, Cl, OMe, 3-isopropyloxypropyl, OCH2), (A1224, Cl, Cl, OMe, 3-isopropyloxybutyl, OCH2), (A1225, Cl, Cl, OMe, 3-isopropyloxypentyl, OCH2), (A1226, Cl, Cl, OMe, 3-isopropyloxyhexyl, OCH2), (A1227, Cl, Cl, OMe, 3-isopropyloxy-4-methylpentyl, OCH2), (A1228, Cl, Cl, OMe, 3-isopropyloxyheptyl, OCH2), (A1229, Cl, Cl, OMe, 3-isopropyloxy-5-methylhexyl, OCH2), (A1230, Cl, Cl, OMe, 3-isopropyloxy-4,4-dimethylpentyl, OCH2), (A1231, Cl, Cl, OMe, 3-isopropyloxyoctyl, OCH2), (A1232, Cl, Cl, OMe, 3-isopropyloxy-5,5-dimethylhexyl, OCH2), (A1233, Cl, Cl, OMe, 3-n-butyloxypropyl, OCH2), (A1234, Cl, Cl, OMe, 3-n-butyloxybutyl, OCH2), (A1235, Cl, Cl, OMe, 3-n-butyloxypentyl, OCH2), (A1236, Cl, Cl, OMe, 3-n-butyloxyhexyl, OCH2), (A1237, Cl, Cl, OMe, 3-n-butyloxy-4-methylpentyl, OCH2), (A1238, Cl, Cl, OMe, 3-n-butyloxyheptyl, OCH2), (A1239, Cl, Cl, OMe, 3-n-butyloxy-5-methylhexyl, OCH2), (A1240, Cl, Cl, OMe, 3-n-butyloxy-4,4-dimethylpentyl, OCH2), (A1241, Cl, Cl, OMe, 3-n-butyloxyoctyl, OCH2), (A1242, Cl, Cl, OMe, 3-n-butyloxy-5,5-dimethylhexyl, OCH2), (A1243, Cl, Cl, OMe, 3-isobutyloxypropyl, OCH2), (A1244, Cl, Cl, OMe, 3-isobutyloxybutyl, OCH2), (A1245, Cl, Cl, OMe, 3-isobutyloxypentyl, OCH2), (A1246, Cl, Cl, OMe, 3-isobutyloxyhexyl, OCH2), (A1247, Cl, Cl, OMe, 3-isobutyloxy-4-methylpentyl, OCH2), (A1248, Cl, Cl, OMe, 3-isobutyloxyheptyl, OCH2), (A1249, Cl, Cl, OMe, 3-isobutyloxy-5-methylhexyl, OCH2), (A1250, Cl, Cl, OMe, 3-isobutyloxy-4,4-dimethylpentyl, OCH2), (A1251, Cl, Cl, OMe, 3-isobutyloxyoctyl, OCH2), (A1252, Cl, Cl, OMe, 3-isobutyloxy-5,5-dimethylhexyl, OCH2), (A1253, Cl, Cl, OMe, 3-t-butyloxypropyl, OCH2), (A1254, Cl, Cl, OMe, 3-t-butyloxybutyl, OCH2), (A1255, Cl, Cl, OMe, 3-t-butyloxypentyl, OCH2), (A1256, Cl, Cl, OMe, 3-t-butyloxyhexyl, OCH2), (A1257, Cl, Cl, OMe, 3-t-butyloxy-4-methylpentyl, OCH2), (A1258, Cl, Cl, OMe, 3-t-butyloxyheptyl, OCH2), (A1259, Cl, Cl, OMe, 3-t-butyloxy-5-methylhexyl, OCH2), (A1260, Cl, Cl, OMe, 3-t-butyloxy-4,4-dimethylpentyl, OCH2), (A1261, Cl, Cl, OMe, 3-t-butyloxyoctyl, OCH2), (A1262, Cl, Cl, OMe, 3-t-butyloxy-5,5-dimethylhexyl, OCH2), (A1263, Cl, Cl, OMe, 3-n-pentyloxypropyl, OCH2), (A1264, Cl, Cl, OMe, 3-n-pentyloxybutyl, OCH2), (A1265, Cl, Cl, OMe, 3-n-pentyloxypentyl, OCH2), (A1266, Cl, Cl, OMe, 3-n-pentyloxyhexyl, OCH2), (A1267, Cl, Cl, OMe, 3-n-pentyloxy-4-methylpentyl, OCH2), (A1268, Cl, Cl, OMe, 3-n-pentyloxyheptyl, OCH2), (A1269, Cl, Cl, OMe, 3-n-pentyloxy-5-methylhexyl, OCH2), (A1270, Cl, Cl, OMe, 3-n-pentyloxy-4,4-dimethylpentyl, OCH2), (A1271, Cl, Cl, OMe, 3-n-pentyloxyoctyl, OCH2), (A1272, Cl, Cl, OMe, 3-n-pentyloxy-5,5-dimethylhexyl, OCH2), (A1273, Cl, Cl, OMe, 3-neopentyloxypropyl, OCH2), (A1274, Cl, Cl, OMe, 3-neopentyloxybutyl, OCH2), (A1275, Cl, Cl, OMe, 3-neopentyloxypentyl, OCH2), (A1276, Cl, Cl, OMe, 3-neopentyloxyhexyl, OCH2), (A1277, Cl, Cl, OMe, 3-neopentyloxy-4-methylpentyl, OCH2), (A1278, Cl, Cl, OMe, 3-neopentyloxyheptyl, OCH2), (A1279, Cl, Cl, OMe, 3-neopentyloxy-5-methylhexyl, OCH2), (A1280, Cl, Cl, OMe, 3-neopentyloxy-4,4-dimethylpentyl, OCH2), (A1281, Cl, Cl, OMe, 3-neopentyloxyoctyl, OCH2), (A1282, Cl, Cl, OMe, 3-neopentyloxy-5,5-dimethylhexyl, OCH2), (A1283, F, F, F, 3-neopentyloxypropyl, CH2CH2), (A1284, F, F, Cl, 3-neopentyloxypropyl, CH2CH2), (A1285, Cl, Cl, F, 3-methyloxyhexyl, CH2CH2), (A1286, Cl, Cl, Cl, 3-methyloxyhexyl, CH2CH2), (A1287, Cl, Cl, F, 3-ethyloxypropyl, CH2CH2), (A1288, Cl, Cl, Cl, 3-ethyloxypropyl, CH2CH2), (A1289, Cl, Cl, F, 3-n-butyloxypropyl, CH2CH2), (A1290, Cl, Cl, Cl, 3-n-butyloxypropyl, CH2CH2), (A1291, Me, Me, Me, 3-methyloxyhexyl, CH2CH2), (A1292, Me, Me, Me, 3-ethyloxypropyl, CH2CH2), (A1293, Me, Me, Me, 3-n-butyloxypropyl, CH2CH2), (A1294, Me, Me, Me, 3-neopentyloxypropyl, CH2CH2)

Example 79
Synthesis of Compound (B1)

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1) Synthesis of 2-[2-fluoro-3-(1-hydoxyhexyl)Phenyl]-2-methyl-1,3-dioxolane (16)

To a THF (48 mL) solution of 2-(2-fluorophenyl)-2-methyl-1,3-dioxolane (6.0 g) and N,N,N′,N″,N″-pentamethyldiethylenetriamine (8.0 mL) was added 1.58 M hexane solution of n-butyl lithium (25.3 mL) dropwise at −78° C. After the reaction mixture was stirred for 1 h, n-hexylaldehyde (5.88 mL) was added into the reaction mixture. After the reaction mixture was stirred for additional 1 h at −78° C., a saturated ammonium chloride aqueous solution was added into the reaction mixture. The reaction mixture was extracted with ethyl acetate, and the organic layer was washed with water, and brine, dried over magnesium sulfate, and evaporated. The obtained residue was purified by colum chromatography (hexane:ethyl acetate=4:1) to obtain the compound (16) 6.9 g.

¹H-NMR(CDCl₃) 7.39-7.46 (m, 2H), 7.11 (t, 1H, J=7.6 Hz), 5.02-5.07 (m, 1H), 4.02-4.11 (m, 2H), 3.82-3.91 (m, 2H), 1.73-1.81 (m, 5H), 1.24-1.70 (m, 6H), 0.86-0.86-0.89 (m, 3H).

2) Synthesis of 2-[2-fluoro-3-(1-methyloxyhexyl)phenyl]-2-methyl-1,3-dioxolane (17)

To a DMF (35 mL) solution of 2-[2-fluoro-3-(1-hydroxyhexyl)phenyl]-2-methyl-1,3-dioxolane e (6.9 g) and methyl iodide (6.1 mL) was added sodium hydride (1.96 g) under ice-cooling. After the reaction mixture was stirred at room temperature for 1 h, a saturated ammonium chloride aqueous solution was added into the reaction mixture. The reaction mixture was extracted with ethyl acetate, and the organic layer was washed with water, and brine, dried over magnesium sulfate, and evaporated. The obtained residue was purified by colum chromatography (hexane:ethyl acetate=20:1) to obtain the compound (17) 6.99 g.

¹H-NMR(CDCl₃) 7.33-7.44 (m, 2H), 7.12 (t, 1H, J=7.6 Hz), 4.56 (dd, 1H, J=7.6 Hz, 2.1 Hz), 4.02-4.14 (m, 2H), 3.85-3.92 (m, 2H), 3.25 (s, 3H), 1.58-1.77 (m, 5H), 1.21-1.46 (m, 6H), 0.86 (t, 3H, J=6.7 Hz).

3) Synthesis of 2-fluoro-3-(1-methyloxyhexyl)acetophenone (18)

To a methanol (10 mL) solution of 2-[2-fluoro-3-(1-methyloxyhexyl)phenyl]-2-methyl-1,3-dioxolane (6.98 g) was added 35% hydrochloric acid (0.5 mL) at room temperature. A saturated sodium hydrogencarbonate aqueous solution was added into the reaction mixture. The reaction mixture was extracted with ethyl acetate, and the organic layer was dried over magnesium sulfate, and evaporated to obtain the compound (18).

¹H-NMR(CDCl₃) 7.40-7.80 (m, 1H), 7.56-7.62 (m, 1H), 7.21-7.26 (t, 1H, J=7.6 Hz), 4.54-4.58 (m, 1H), 3.26 (s, 3H), 2.66 (d, 3H, J=4.9 Hz), 1.62-1.77 (m, 2H), 1.29-1.44 (m, 6H), 0.85-0.90 (m, 3H).

4) Synthesis of 4-[2-fluoro-3-(1-methyloxyhexyl)phenyl]thiazol-2-ylamine (19)

To a 10% methanol-chloroform (60 mL) solution of 2-fluoro-3-(1-methyloxyhexyl)acetophenone was added bromine (1.21 mL), and the reaction miture was stirred for 1 h. After the solvent was evaporated, the residue was dissolved in ethanol (60 mL), and thiourea (1.8 g) was added into the reaction mixture. The reaction mixture was heated at reflux for 7 h, and evaporated. A saturated sodium hydrogencarbonate aqueous solution was added into the residue, and the mixture was extracted with ethyl acetate, dried over magnesium sulfate, and evaporated. The obtained residue was purified by colum chromatography (hexane:ethyl acetate=4:1) to obtain the compound (19) 5.0 g.

¹H-NMR(CDCl₃) 7.92 (dt, 1H, J=7.6 Hz, 1.8 Hz), 7.28-7.34 (m, 1H), 7.20 (t, 1H, J=7.6 Hz), 7.02 (d, 1H, J=2.4 Hz), 4.56-4.60 (m, 1H), 3.25 (s, 3H), 1.63-1.83 (m, 2H), 1.24-1.47 (m, 6H), 0.81-0.89 (m, 3H).

5) Synthesis of Ethyl 3-(2,6-difluoro-4-{4-[2-fluoro-3-(1-methyloxyhexyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylate (20)

To a DMF (6 mL) solution of 4-[2-fluoro-3-(1-methyloxyhexyl)phenyl]thiazol-2-ylamine (318 mg), 3-(4-bromo-2,6-difluoropheny)-2-methylacrylic acid ethyl ester (300 mg), and dichlorobistriphenylphosphinepalladium (36 mg) was added triethylamine (0.43 mL). The reaction mixture was stirred under carbon monoxide atomosphere at 85° C. for 16 h. Water was poured into the reaction mixture, and the reaction mixture extracted with ethyl acetate, and the organic layer was washed with water, and brine, dried over magnesium sulfate, and evaporated. The obtained residue was purified by colum chromatography (hexane:ethyl acetate=4:1) to obtain the compound (20) 500 mg.

6) Synthesis of 3-(2,6-difluoro-4-{4-[2-fluoro-3-(1-methyloxyhexyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1)

To a mixture of THF (2 mL), methanol (2 mL), and 2N sodium hydroxide aqueous solution of 3-(2,6-difluoro-4-{4-[2-fluoro-3-(1-methyloxyhexyl)phenyl]thiazol-2-ylcarbamoyl}phenyl}-2-methylacrylic acid ethyl ester (500 mg) was stirred at room temperature for 3 h. The reaction mixture was acidified with hydrochloric acid, and extracted with ethyl acetate. The organic layer was washed with water, and brine, dried over magnesium sulfate, and evaporated. The residue was recrystallized from ethyl acetate to obtain the compoumd (B1) 370 mg.

1H-NMR(DMSO-d6) 13.02 (bs, 2H), 7.94-8.08 (m, 3H), 7.66 (d, 1H, J=2.1Hz), 7.30-7.42 (m, 3H), 4.57 (t, 1H, J=6.4 Hz), 3.18 (s, 3H), 1.81 (s, 3H), 1.60-1.81 (m, 2H), 1.20-1.50 (m, 6H), 0.80-0.90 (m, 3H).

Example 80
Synthesis of Compound (B533)

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1) Synthesis of (methyloxymethyloxycarbonylmethyl)triphenylphosphonium chloride (22)

Methyl dimethyloxyacetate (15 g) was dissolved in acetyl chloride (9.7 g), and iodine (0.09 g) was added into the mixture. The reaction mixture was stirred for 3 h, and evaporated. The residue was dissolved again in dichloromethane (200 mL), and triphenylphospkine (29.5 g) was added into the reaction mixture. The reaction mixture was stirred for 3 h, and evaporated to obtain the compound (22) 44 g.

¹H-NMR(CDCl₃) 7.96-8.03 (m, 6H), 7.63-7.78 (m, 9H), 3.90 (s, 3H), 3.60 (s, 1H).

2) Syntehsis of Methyl (Z)-3-(4-bromo-2,6-difluorophenyl)-2-methyloxyacrylate (23)

4-Bromo-2,6-difluorobenzaldehyde (31.2 g) was dissolved in dichloromethane (300 mL), and (methyloxymethyloxycarbonylmethyl)triphenylphosphonium chloride (113.3 g) was added into the mixture. To the reaction mixture was added triethylamine (59 mL) dropwise, and the reaction mixture was stirred for 3 h. To the reaction mixture were added ice-water and 2N hydrochloric acid, and the reaction mixture was extracted with ethyl acetate. The organic layer was washed with water, and brine, dried over magnesium sulfate, evaporated. The obtained residue was purified by colum chromatography (hexane:ethyl acetate=10:1) to obtain the compound (23) 32.1 g.

¹H-NMR(CDCl₃) 7.08-7.14 (m, 2H), 6.67-6.68 (m, 1H), 3.87 (s, 3H), 3.76 (s, 3 h).

3) Syntehsis of Methyl (Z)-3-(2,6-difluoro-4-{4-[2-fluoro-3-(1-methyloxyhexyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methyloxyacrylate (24)

4-[2-Fluoro-3-(1-methyloxyhexyl)phenyl]thiazol-2-ylamine (460 mg) and methyl (Z)-3-(4-bromo-2,6-difluorophenyl)-2-methyloxyacrylate (462 mg), and dichlorobistriphenylphosphinepalladium (150 mg) were dissolved in DMF (6 mL). Triethylamine (0.84 mL) was added into the mixture, and the reaction mixture was stirred under carbon monoxide atomosphere at 85° C. for 16 h. Water added into the reaction mixture, and the reaction mixture was extracted with ethyl acetate. The organic layer was washed with water, and brine, dried over magnesium sulfate, evaporated. The obtained residue was purified by colum chromatography (hexane:ethyl acetate=4:1) to obtain the compound (24) 630 mg.

1H-NMR(DMSO-d6) 12.98 (bs, 2H), 8.01-8.05 (m, 1H), 7.89-7.95 (m, 2H), 7.65 (d, 1H, J=2.4 Hz), 7.31-7.39 (m, 2H), 6.66 (s, 1H), 4.55-4.60 (m, 1H), 3.80 (s, 3H), 3.18 (s, 3H), 1.64-1.76 (m, 2H), 1.26-1.41 (m, 6H), 0.81-0.86 (m, 3H).

4) Syntehsis of (Z)-3-(2,6-difluoro-4-{4-[2-fluoro-3-(1-methyloxyhexyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methyloxyacrylic acid (B533)

Methyl (Z)-3-(2,6-difluoro-4-{4-[2-fluoro-3-(1-methyloxyhexyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methyloxyacrylate (630 mg) was dissolved in a mixture of THF (2 mL), methanol (2 mL), and 2N sodium hydroxide aqueous solution (2 mL), and the mixture was stirred at room temperature for 3 h. The reaction mixture was acidified with hydrochloric acid, and the reaction mixture was extracted with ethyl acetate. The organic layer was washed with water, and brine, dried over magnesium sulfate, evaporated. The obtained residue was recrystallized from ethyl acetate to obtain the compound (B533) 590mg.

1H-NMR(DMSO-d6) 12.98 (bs, 2H), 8.00-8.05 (m, 1H), 7.89-7.95 (m, 2H), 7.65 (d, 1H, J=2.4 Hz), 7.31-7.39 (m, 2H), 6.67 (s, 1H), 4.55-4.59 (m, 1H), 3.72 (s, 3H), 1.64-1.76 (m, 2H), 1.26-1.41 (m, 6H), 0.81-0.86 (m, 3H).

B2 to B101, B121, B122, B134, B169, B170, B195, B216, B233, B255, B264, B347 to B349, B354, B355, B380, B397, B418, B419, B425, B488, B505, B519, B521, B790, B896, B897, B899, B905, B927, B936, B958, B967, B1053, B1054, B1059, B1060, B1102, B1122, B1124, B1238, B1250, B1429, B1432, B1438, B1728 to B1739, B1742, B1744, B1746 to B1757, B1762 to B2047, B2049, B2051 to B2090, and B2097 to B2100 were synthsized by similar method mentioned above.

Example 81
Syntehsis of 3-(2,6-difluoro-4-{4-[3-(3,3-dimethylbutyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B2)

1H-NMR(DMSO-d6) 13.01(bs, 2H), 7.88-8.02 (m, 3H), 7.64 (d, 1H, J=2.4 Hz), 7.34 (s, 1H), 7.28 (dt, 1H, J=7.0 Hz, 1.5 Hz), 7.22 (t, 1H, J=7.6 Hz), 2.60-2.70 (m, 2H), 1.81 (d, 3H, J=1.5 Hz), 1.42-1.55 (m, 2H), 0.97 (s, 9H).

Example 82
Syntehsis of 3-(4-{4-[3-(1-cyclohexyl-1-methyloxymethyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methylacrylic acid (B3)

1H-NMR(DMSO-d6) 13.02 (bs, 2H), 7.93-8.08 (m, 3H), 7.65 (d, 1H, J=2.4 Hz), 7.28-7.48 (m, 3H), 4.32 (d, 1H, J=7.0 Hz), 3.15 (s, 3H), 1.90 (m, 1H), 1.81 (d, 3H, J=1.5 Hz), 0.90-1.80 (m, 10H).

Example 83
Syntehsis of 3-{2,6-difluoro-4-[4-(2-fluoro-3-pentylphenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methylacrylic acid (B4)

1H-NMR(DMSO-d6) 13.01 (bs, 2H), 7.90-8.02 (m, 3H), 7.64 (d, 1H J=2.1 Hz), 7.34 (s, 1H), 7.18-7.32 (m, 2H), 2.68 (t, 2H, J=7.6 Hz), 1.81 (s, 3H), 1.61 (t, 2H, J=6.9 Hz), 1.20-1.40 (m, 4H), 0.88 (t, 3H, J=6.0 Hz).

Example 84
Syntehsis of 3-(2,6-difluoro-4-{4-[2-fluoro-3-(4-methylpentyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B5)

1H-NMR(DMSO-d6) 13.01 (bs, 2H), 7.90-8.02 (m, 3H), 7.64 (s, 1H), 7.34 (s, 1H), 7.18-7.33 (m, 2H), 2.67 (t, 2H, J=7.2 Hz), 1.81 (s, 3H), 1.50-1.70 (m, 3H), 1.19-1.36 (m, 2H), 0.86 (d, 6H, J=6.7 Hz).

Example 85
Syntehsis of 3-(4-{4-[3-(1-cyclohexyl-1-ethyloxymethyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methylacrylic acid (B6)

1H-NMR(DMSO-d6) 13.02 (bs, 2H), 8.00-8.06 (m, 2H), 7.97 (d, 1H, J=8.5 Hz), 7.64 (d, 1H, J=2.7 Hz), 7.30-7.38 (m, 3H), 4.41 (d, 1H, J=7.3 Hz), 3.23-3.40 (m, 2H), 1.94 (m, 1H), 1.81(d, 3H, J=1.5 Hz), 0.90-1.75 (m, 10H), 1.10 (t, 3H, J=7.0 Hz).

Example 86
Syntehsis of 3-(2,6-difluoro-4-{4-[2-fluoro-3-(2,4-dimethyl-3-methyloxy-3-pentyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B7)

1H-NMR(DMSO-d6) 13.00 (bs, 2H), 7.91-8.08 (m, 3H), 7.57 (d, 1H, J=3.1 Hz), 7.30-7.42 (m, 3H), 3.32 (s, 3H), 2.50-2.70 (m, 2H), 1.81 (s, 3H), 0.90 (d, 12H, J=6.7 Hz).

Example 87
Syntehsis of 3-(2,6-difluoro-4-{4-[2-fluoro-3-(4-methyloxy-4-pentyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B8)

1H-NMR(DMSO-d6) 13.00 (bs, 2H), 7.93-8.04 (m, 3H), 7.62 (d, 1H, J=2.7 Hz), 7.51 (dt, 1H, J=1.8, 7.8 Hz), 7.35 (s, 1H), 7.27 (t, 1H, J=7.8 Hz), 3.17 (s, 3H), 1.82-2.02 (m, 4H), 1.81 (d, 3H, J=1.5 Hz), 0.75-1.35 (m, 10H).

Example 88
Syntehsis of 3-(2,6-difluoro-4-{4-[2-fluoro-3-(1-methyloxydecyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B9)

1H-NMR(DMSO-d6) 13.01 (bs, 2H), 7.92-8.08 (m, 3H), 7.65 (d, 1H, J=2.4 Hz), 7.30-7.41 (m, 3H), 4.57 (t, 1H, J=6.4 Hz), 3.18 (s, 3H), 1.81 (d, 3H, J=1.8 Hz), 1.60-1.80 (m, 2H), 1.15-1.40 (m, 14H), 0.84 (t, 3H, J=6.5 Hz).

Example 89
Syntehsis of 3-(2,6-difluoro-4-{4-[3-(1-ethyloxy-2,2-dimethylpropyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B10)

1H-NMR(DMSO-d6) 13.01 (bs, 2H), 7.93-8.08 (m, 3H), 7.62 (d, 1H, J=2.7 Hz), 7.30-7.40 (m, 3H), 4.42 (s, 1H), 3.20-3.40 (m, 2H), 1.81 (d, 3H, J=1.5 Hz), 1.11 (t, 3H, J=7.0 Hz), 0.91 (s, 9H).

Example 90
Syntehsis of 3-(2,6-difluoro-4-{4-[2-fluoro-3-(1-methyloxy-4-methylpentyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B11)

1H-NMR(DMSO-d6) 13.03 (bs, 2H), 7.93-8.08 (m, 3H), 7.66 (d, 1H, J=2.7 Hz), 7.30-7.43 (m, 3H), 4.55 (t, 1H, J=6.6 Hz), 3.18 (s, 3H), 1.81 (s, 3H), 1.10-1.85 (m, 5H), 0.84 (d, 6H, J=6.7 Hz).

Example 91
Syntehsis of 3-(2,6-difluoro-4-{4-[2-fluoro-3-(4-methyloxyhexyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B12)

1H-NMR(DMSO-d6) 13.00 (bs, 2H), 7.93-7.98 (m, 3H), 7.64 (d, 1H, J=2.3 Hz), 7.20-7.34 (m, 3H), 3.20 (s, 3H), 3.10 (qint, 1H, J=5.6 Hz), 2.69 (t, 2H, J=7.7 Hz), 3.18 (s, 3H), 1.81 (d, 3H, J=1.6 Hz), 1.57-1.67 (m, 2H), 1.39-1.50 (m, 4H), 0.81 (t, 3H, J=7.5 Hz).

Example 92
Syntehsis of 3-(2,6-difluoro-4-{4-[2-fluoro-3-(1-methyloxy-2,2-dimethylpropyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B13)

1H-NMR(DMSO-d6) 13.00 (bs, 2H), 7.94-8.06 (m, 3H), 7.63 (d, 1H, J=2.7 Hz), 7.28-8.38 (m, 3H), 4.32 (s, 1H), 3.14 (s, 3H), 1.81 (d, 3H, J=1.6 Hz), 0.91 (2, 9H).

Example 93
Syntehsis of 3-(4-{4-[3-(1-cyclohexyl-1-n-pentyloxymethyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methylacrylic acid (B14)

1H-NMR(DMSO-d6) 13.01 (bs, 2H), 7.99 (m, 1H), 7.98 (s, 1H), 7.95 (s, 1H), 7.64 (d, 1H, J=2.4 Hz), 7.28-7.36 (m, 3H), 4.39 (d, 1H, J=6.9 Hz), 3.24 (t, 2H, J=5.7 Hz), 1.93 (m, 1H), 1.81 (d, 3H, J=1.8 Hz), 0.94-1.76 (m, 16H), 0.84 (t, 3H, J=7.2 Hz).

Example 94
Syntehsis of 3-(2,6-difluoro-4-{4-[3-(2,2-dimethyl-1-n-pentyloxypropyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B15)

1H-NMR(DMSO-d6) 13.02 (bs, 2H), 7.96-8.05 (m, 3H), 7.62 (s, 1H), 7.26-7.37 (m, 3H), 4.39 (s, 1H), 3.22 (t, 2H, J=6.6 Hz), 1.81 (s, 3H), 1.44-1.57 (m, 2H), 1.19-1.38 (m, 4H), 0.91 (2, 9H), 0.84-0.88 (m, 3H).

Example 95
Syntehsis of 3-(2,6-difluoro-4-{4-[2-fluoro-3-(3-methylthio-1-n-pentyloxypropyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B16)

1H-NMR(DMSO-d6) 13.00 (bs, 2H), 7.94-8.05 (m, 3H), 7.66 (d, 1H, J=2.4 Hz), 7.32-7.42 (m, 3H), 4.82 (m, 1H), 3.28-3.50 (m, 2H), 2.58 (t, 2H, J=7.8 Hz), 2.06 (s, 3H), 1.87-2.02 (m, 2H), 1.81 (d, 3H, J=1.5 Hz), 1.44-1.58 (m, 2H), 1.20-1.35 (m, 4H), 0.85 (t, 3H, J=6.9 Hz).

Example 96
Syntehsis of 3-(2,6-difluoro-4-{4-[2-fluoro-3-(3-methyloxy-3-methylbutyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B17)

1H-NMR(DMSO-d6) 13.01 (bs, 2H), 7.90-8.00 (m, 3H), 7.64 (d, 1H, J=2.4 Hz), 7.12-7.34 (m, 3H), 3.14 (s, 3H), 2.64-2.70 (m, 2H), 1.81 (d, 3H, J=1.5 Hz), 1.69-1.75 (m, 2H), 1.17 (s, 6H).

Example 97
Syntehsis of 3-[2,6-difluoro-4-(4-{2-fluoro-3-{1-(3-methylbutyloxypropyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B18)

1H-NMR(DMSO-d6) 13.02 (bs, 2H), 7.95-8.04 (m, 3H), 7.64 (d, 1H, J=2.7 Hz), 7.31-7.40 (m, 3H), 4.59 (t, 1H, J=6.6 Hz), 3.08-3.50 (m, 2H), 1.81 (d, 3H, J=1.5 Hz), 1.65-1.76 (m, 3H), 1.41 (q, 2H, J=6.6 Hz), 0.81-0.91 (m, 9H).

Example 98
Syntehsis of 3-(2,6-difluoro-4-{4-[2-fluoro-3-(1-n-pentyloxypropyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B19)

1H-NMR(DMSO-d6) 13.01 (bs, 2H), 7.91-8.06 (m, 3H), 7.65.(d, 1H, J=2.4 Hz), 7.31-7.41 (m, 3H), 4.59 (t, 1H, J=6.6 Hz), 3.25-3.38 (m, 2H), 1.81 (d, 3H, J=1.8 Hz), 1.64-1.77 (m, 2H), 1.46-1.57 (m, 2H), 1.20-1.35 (m, 4H), 0.89 (t, 3H, J=7.2 Hz), 0.85 (t, 3H, J=7.2 Hz).

Example 99
Syntehsis of 3-[4-(4-{3-(2,2-dimetylpropyloxy)propyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methylacrylic acid (B20)

1H-NMR(DMSO-d6) 13.00 (bs, 2H), 7.92-8.02 (m, 3H), 7.63 (s, 1H), 7.34 (s 1H), 7.22-7.30 (m, 2H), 3.42 (t, 2H, J=6.0 Hz), 3.04 (s, 2H), 2.76 (t, 2H, J=7.8 Hz), 1.81-1.89 (m, 5H), 0.89 (s, 9H).

Example 100
Syntehsis of 3-[4-(4-{3-[1-cyclohexyl-1-(4-ethyloxybutyloxy)methyl]-2-fluorophenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methylacrylic acid (B21)

1H-NMR(DMSO-d6) 13.02 (bs, 2H), 7.95-8.04 (m, 3H), 7.64 (d, 1H, J=2.4 Hz), 7.33 (d, 3H, J=7.2 Hz), 4.39 (d, 1H, J=6.9 Hz), 3.25-3.39 (m, 6H), 1.95 (m, 1H), 1.81 (d, 3H, J=1.8 Hz), 1.45-1.76 (m, 9H), 1.36 (m, 1H), 0.98-1.23 (m, 4H), 1.07 (t, 3H, J=6.6 Hz).

Example 101
Syntehsis of 3-[2,6-difluoro-4-(4-{3-[1-(4-ethyloxybutyloxy)propyl]-2-fluorophenyl}thiazol-2-ylcarbamoyl)phenyl]-2-methylacrylic acid (B22)

1H-NMR(DMSO-d6) 13.00 (bs, 2H), 7.95-8.04 (m, 3H), 7.64 (d, 1H, J=2.4 Hz), 7.31-7.40 (m, 3H), 4.60 (t, 1H, J=5.7 Hz), 3.33-3.37 (m, 6H), 1.81 (d, 3H, J=1.5 Hz), 1.64-1.77 (m, 2H), 1.54 (s, 4H), 1.07 (t, 3H, J=6.9 Hz), 0.89 (t, 3H, J=7.2 Hz).

Example 102
Syntehsis of 3-(2,6-difluoro-4-{4-[2-fluoro-3-(1-methyloxyheptyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B23)

1H-NMR(DMSO-d6) 13.00 (bs, 1H), 7.95-8.05 (m, 3H), 7.64 (d, 1H, J=2.4 Hz), 7.23-7.33 (m, 3H), 4.54 (t, 1H, J=6.5 Hz), 3.18 (s, 3H,), 1.81 (d, 3H, J=1.3 Hz), 1.60-1.80 (m, 4H), 1.20-1.30 (m, 6H), 0.81-0.85 (m, 3H).

Example 103
Syntehsis of 3-(2,6-difluoro-4-{4-[3-(1-ethyloxybutyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B24)

1H-NMR(DMSO-d6) 13.00 (bs, 2H), 7.94-8.04 (m, 3H), 7.65 (d, 1H, J=2.4 Hz), 7.31-7.42 (m, 3H), 4.67-4.71 (m, 1H), 3.36 (t, 2H, J=7.0 Hz), 1.81 (d, 3H, J=1.5 Hz), 1.60-1.78 (m, 2H), 1.27-1.44 (m, 2H), 1.12 (t, 3H, J=7.0 Hz), 0.89 (t, 3H, J=7.3 Hz).

Example 104
Syntehsis of 3-(2,6-difluoro-4-{4-[2-fluoro-3-(1-methyloxyoctyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B25)

1H-NMR(DMSO-d6) 13.00(bs, 2H), 7.95-8.05(m, 3H), 7.65(d, 1H, J=2.7 Hz), 7.31-8.38 (m, 3H), 4.56(t, 1H, J=6.5 Hz), 3.18(s, 3H), 1.81(d, 3H, J=1.4 Hz), 1.60-1.81 (m, 2H), 1.20-1.37 (m, 10H), 0.81-0.86 (m, 3H).

Example 105
Syntehsis of 3-(2,6-difluoro-4-{4-[2-fluoro-3-(1-n-pentyloxypentyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B26)

1H-NMR(DMSO-d6) 13.01(bs, 2H), 7.94-8.04 (m, 3H), 7.65 (d, 1H, J=2.0 Hz), 7.30-7.40 (m, 3H), 4.62-4.66 (m, 1H), 3.28 (t, 2H, J=6.4 Hz), 1.80 (s, 3H), 1.60-1.75 (m, 2H), 1.45-1.54 (m, 2H), 1.22-1.33 (m, 8H), 0.83-0.87 (m, 6H).

Example 106
Syntehsis of 3-(2,6-difluoro-4-{4-[3-(1-ethyloxypentyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B27)

1H-NMR(DMSO-d6) 13.01 (bs, 2H), 7.95-8.04 (m, 3H), 7.64-7.65 (m, 1H), 7.30-7.41 (m, 3H), 4.67 (t, 1H, J=6.9 Hz), 3.35 (q, 2H, J=6.9 Hz), 1.81 (d, 3H, J=1.3 Hz), 1.60-1.81 (m, 2H), 1.23-1.41 (m, 4H), 1.12 (t, 3H, J=6.9 Hz), 0.83-0.87 (m, 3H).

Example 107
Syntehsis of 3-(2,6-difluoro-4-{4-[2-fluoro-3-(1-methyloxynonyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B28)

1H-NMR(DMSO-d6) 13.02 (bs, 2H), 7.95-8.05 (m, 3H), 7.65 (d, 1H, J=2.7 Hz), 7.31-7.39 (m, 3H), 4.56 (t, 1H, J=7.2 Hz), 3.18 (s, 3H), 1.81 (s, 3H), 1.55-1.85 (m, 2H), 1.17-1.45(m, 12H), 0.83 (t, 3H, J=6.3 Hz).

Example 108
Syntehsis of 3-(2,6-difluoro-4-{4-[2-fluoro-3-(3-methyloxydecyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B29)

1H-NMR(DMSO-d6) 13.00 (bs, 1H), 7.90-7.98(m, 3H), 7.64(d, 1H, J=2.4 Hz), 7.23-7.33 (m, 3H), 3.33 (s, 3H,), 3.20-3.28 (m, 1H,), 2.65-2.70 (m, 2H,), 1.81 (d, 3H, J=1.4 Hz), 1.70-1.80 (m, 2H), 1.32-1.40 (m, 2H), 1.20-1.30 (m, 6H), 0.81-0.85 (m, 3H).

Example 109
Syntehsis of 3-(2,6-difluoro-4-{4-[2-fluoro-3-(1-n-octyloxyethyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B30)

1H-NMR(DMSO-d6) 13.00 (bs, 2H), 7.95-8.03 (m, 5H), 7.64 (d, 1H, J=2.3 Hz), 7.30-7.42 (m, 5H), 4.81 (q, 1H, J=6.4 Hz), 3.23-3.40 (m, 2H), 1.81 (s, 3H), 1.48-1.52 (m, 2H), 1.40 (d, 3H, J=6.4 Hz), 1.22-1.29 (m, 10H), 0.82-0.86 (m, 3H).

Example 110
Syntehsis of 3-(2,6-difluoro-4-{4-[2-fluoro-3-(1-n-pentyloxyethyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B31)

1H-NMR(DMSO-d6) 13.00 (bs, 2H), 7.95-8.04 (m, 3H), 7.65 (d, 1H, J=2.3 Hz), 7.30-8.43 (m, 3H), 4.80 (q, 1H, J=6.3 Hz), 3.23-3.34 (m, 2H), 1.48-1.55 (m, 2), 1.41 (d, 3H, J=6.4 Hz), 1.22-1.30 (m, 4H), 0.83-0.88 (m, 3H).

Example 111
Syntehsis of 3-(2,6-difluoro-4-{4-[2-fluoro-3-(n-decyloxymethyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B32)

1H-NMR(DMSO-d6) 13.00 (bs, 2H), 8.04 (dt, 1H, J=7.7 Hz, 1.8 Hz), 7.94-7.99 (m, 2H), 7.65 (d, 1H, J=2.5 Hz), 7.42 (t, 1H, J=7.0 Hz), 7.28-7.33 (m, 2H), 4.57 (s, 2H), 3.48 (t, 2H, 6.6 Hz), 1.81 (d, 3H, J=1.3 Hz), 1.51-1.58 (m, 2H), 1.22-1.35 (m, 14H), 0.81-0.86 (m, 3H).

Example 112
Syntehsis of 3-(2,6-difluoro-4-{4-[2-fluoro-3-(n-pentyloxymethyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B33)

1H-NMR(DMSO-d6) 13.02 (bs, 2H), 8.04 (dt, 1H, J=7.5 Hz, 1.9 Hz), 7.39-7.99 (m, 2H), 7.65 (d, 1H, J=2.7 Hz), 7.40-7.44 (m, 1H), 7.28-7.34 (m, 2H), 4.58 (s, 2H), 3.49 (t, 2H, 6.4 Hz), 1.81 (d, 3H, J=1.4 Hz), 1.51-1.60 (m, 2H), 1.28-1.32 (m, 4H), 0.84-0.89 (m, 3H).

Example 113
Syntehsis of 3-(2,6-difluoro-4-{4-[2-fluoro-3-(1-n-propyloxybutyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B34)

1H-NMR(DMSO-d6) 13.00 (bs, 1H), 7.95-8.05(m, 3H), 7.65(d, 1H, J=2.4 Hz), 7.30-7.38 (m, 3H), 4.67 (t, 1H, J=6.4 Hz), 3.22 (t, 2H, J=6.5), 1.81 (d, 3H, J=1.3 Hz), 1.30-1.84 (m, 6H), 0.81-0.85 (m, 6H).

Example 114
Syntehsis of 3-(4-{4-[3-(1-n-butyloxybutyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methylacrylic acid (B35)

1H-NMR(DMSO-d6) 13.00 (bs, 1H), 7.95-8.04(m, 3H), 7.64(d, 1H, J=2.4 Hz), 7.30-7.38 (m, 3H), 4.67 (t, 1H, J=6.4 Hz), 3.22 (t, 2H, J=6.5), 1.81 (d, 3H, J=1.4 Hz), 1.30-1.84 (m, 8H), 0.81-0.85 (m, 6H).

Example 115
Syntehsis of 3-(2,6-difluoro-4-{4-[2-fluoro-3-(1-n-pentyloxybutyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B36)

1H-NMR(DMSO-d6) 13.00 (bs, 1H), 7.94-8.04(m, 3H), 7.64(d, 1H, J=2.3 Hz), 7.30-7.38 (m, 3H), 4.66 (t, 1H, J=6.5 Hz), 3.22 (t, 2H, J=6.5), 1.81 (d, 3H, J=1.4 Hz), 1.26-1.70 (m, 10H), 0.81-0.85 (m, 6H).

Example 116
Syntehsis of 3-(4-{4-[3-(1-n-butyloxypropyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methylacrylic acid (B37)

1H-NMR(DMSO-d6) 13.00 (bs, 2H), 7.94-8.03 (m, 3H), 7.64 (d, 1H, J=2.4 Hz), 7.31-7.40 (m, 3H), 4.59 (t, 1H, J=6.6 Hz), 3.25-3.33 (m, 2H), 1.81 (d, 3H, J=1.5 Hz), 1.64-1.76 (m, 2H), 1.44-1.55 (m, 2H), 1.28-1.40 (m, 2H), 0.89 (t, 3H, J=7.2 Hz), 0.86 (t, 3H, J=7.2 Hz).

Example 117
Syntehsis of 3-(2,6-difluoro-4-{4-[2-fluoro-3-(1-n-hexyloxypropyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B38)

1H-NMR(DMSO-d6) 13.01 (bs, 2H), 7.95-8.03 (m, 3H), 7.65 (s, 1H), 7.30-7.39 (m, 3H), 4.58 (t, 1H, J=6.0 Hz), 3.18-3.47 (m, 2H), 1.81 (d, 3H, J=1.5 Hz), 1.64-1.79 (m, 2H), 1.44-1.56 (m, 2H), 1.16-1.37 (m, 6H), 0.89 (t, 3H, J=7.5 Hz), 0.84 (t, 3H, J=6.6 Hz).

Example 118
Syntehsis of 3-[2,6-difluoro-4-(4-(2-fluoro-3-[3-(4-methylpentyloxy)propyl]phenyl}thiazol-2-ylcarbamoyl)phenyl]-2-methylacrylic acid (B39)

1H-NMR(DMSO-d6) 13.00 (bs, 2H), 7.91-7.95 (m, 3H), 7.63 (d, 1H, J=2.4 Hz), 7.34 (s, 1H), 7.21-7.30 (m, 2H), 3.20-3.44 (m, 4H), 2.73 (t, 2H, J=7.2 Hz), 1.76-1.90 (m, 2H), 1.80 (s, 3H), 1.44-1.56 (m, 4H), 1.14-1.25 (m, 2H), 0.86 (d, 6H, J=6.6 Hz).

Example 119
Syntehsis of 3-[2,6-difluoro-4-(4-{3-[3-(3,3-dimethylbutyloxy)propyl]-2-fluorophenyl}thiazol-2-ylcarbamoyl)phenyl]-2-methylacrylic acid (B40)

1H-NMR(DMSO-d6) 13.02 (bs, 2H), 7.91-7.98 (m, 3H), 7.63 (d, 1H, J=2.4 Hz), 7.34 (s, 1H), 7.21-7.30 (m, 2H), 3.37-3.41 (m, 4H), 2.74 (t, 2H, J=7.2 Hz), 1.81 (d, 3H, J=1.8 Hz), 1.78-1.87 (m, 2H), 1.44 (t, 2H, J=7.5 Hz), 0.90 (s, 9H).

Example 120
Syntehsis of 3-(2,6-difluoro-4-{4-[2-fluoro-3-(1-n-propyloxypentyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B41)

1H-NMR(DMSO-d6) 13.00 (bs, 2H), 7.93-8.04 (m, 3H), 7.65 (d, 1H, J=2.0 Hz), 7.31-7.41 (m, 3H), 4.63-4.67 (m, 1H), 3.25 (t, 2H, J=6.6 Hz), 1.64-1.81 (m, 5), 1.52 (q, 2H, J=6.9 Hz), 1.26-1.40 (m, 4H), 0.82-0.90 (m, 6H).

Example 121
Syntehsis of 3-(4-{4-[3-(1-n-butyloxypentyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl]-2-methylacrylic acid (B42)

1H-NMR(DMSO-d6) 13.01 (bs, 2H), 7.94-8.03 (m, 3H), 7.65 (d, 1H, J=2.3 Hz), 7.31-7.41 (m, 3H), 4.63-4.67 (m, 1H), 3.29 (t, 2H, J=6.4 Hz), 1.81 (s, 3H), 1.60-1.78 (m, 2H), 1.44-1.53 (m, 2H), 1.28-1.40 (m, 6H), 0.86 (t, 6H, J=7.2 H).

Example 122
Syntehsis of 3-[2,6-difluoro-4-(4-{3-[3-(2-ethylbutyloxy)propyl]-2-fluorophenyl}thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B43)

1H-NMR(DMSO-d6) 13.00 (bs, 2H), 7.91-7.99 (m, 3H), 7.63 (d, 1H, J=2.4 Hz), 7.34 (s, 1H), 7.21-7.30 (m, 2H), 3.25-3.42 (m, 4H), 2.74 (t, 2H, J=7.8 Hz), 1.80-1.88 (m, 2H), 1.81 (d, 3H, J=2.1 Hz), 1.25-1.42 (m, 5H), 0.85 (t, 6H, J=7.5 Hz).

Example 123
Syntehsis of 3-[4-(4-{3-[3-(2-cyclopentylethyloxy)propyl]-2-fluorophenyl}thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methylacrylic acid (B44)

1H-NMR(DMSO-d6) 13.00 (bs, 2H), 7.91-7.98 (m, 3H), 7.63 (d, 1H, J=2.7 Hz), 7.34 (s, 1H), 7.20-7.30 (m, 2H), 3.24-3.44 (m, 4H), 2.74 (t, 2H, J=7.2 Hz), 1.81 Hz), (d, 3H, J=1.8 Hz), 1.66-1.89 (m, 4H), 1.40-1.64 (m, 5H), 1.00-1.14 (m, 4H).

Example 124
Syntehsis of 3-(2,6-difluoro-4-{4-[2-fluoro-3-(3-n-pentyloxypropyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B45)

1H-NMR(DMSO-d6) 13.01 (bs, 2H), 7.91-7.98 (m, 3H), 7.64 (d, 1H, J=2.4 Hz), 7.34 (s, 1H), 7.21-7.30 (m, 2H), 3.24-3.41 (m, 4H), 2.74 (t, 2H, J=7.8 Hz), 1.77-1.90 (m, 2H), 1.81 (d, 3H, J=1.8 Hz), 1.44-1.55 (m, 2H), 1.23-1.36 (m, 4H), 0.84-0.89 (m, 3H).

Example 125
Syntehsis of 3-(2,6-difluoro-4-{4-[2-fluoro-3-(3-n-hexyloxypropyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B46)

1H-NMR(DMSO-d6) 13.01 (bs, 2H), 7.91-7.99 (m, 3H), 7.64 (d, 1H, J=2.7 Hz), 7.34 (s, 1H), 7.21-7.30 (m, 2H), 3.20-3.42 (m, 4H), 2.74 (t, 2H, J=7.2 Hz), 1.77-1.87 (m, 2H), 1.81 (d, 3H, J=1.8 Hz), 1.45-1.51 (m, 2H), 1.20-1.36 (m, 6H), 0.86 (t, 3H, J=6.9 Hz).

Example 126
Syntehsis of 3-(2,6-difluoro-4-{4-[2-fluoro-3-(1-methyloxyundecyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B47)

1H-NMR(DMSO-d6) 13.01 (bs, 2H), 7.94-8.05 (m, 3H), 7.65 (d, 1H, J=2.7 Hz), 7.31-7.39 (m, 3H), 4.54-4.58 (m, 1H), 3.18 (s, 3H), 1.81 (s, 3H), 1.60-1.80 (m, 2H), 1.21-1.36 (m, 16H), 0.81-0.86 (m, 3H).

Example 127
Syntehsis of 3-(2,6-difluoro-4-{4-[2-fluoro-3-(1-methyloxydodecyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B48)

1H-NMR(DMSO-d6) 13.01 (bs, 2H), 7.94-8.05 (m, 3H), 7.64 (d, 1H, J=2.5 Hz), 7.30-7.38 (m, 3H), 4.54-4.58 (m, 1H), 3.17 (s, 3H), 1.81 (d, 3H, J=1.4 Hz), 1.61-1.81 (m, 2H), 1.21-1.36 (m, 18H), 0.81-0.85 (m, 3H).

Example 128
Syntehsis of 3-(4-{4-[3-(3-n-butyloxypropyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methylacrylic acid (B49)

1H-NMR(DMSO-d6) 13.02 (bs, 2H), 7.91-8.00 (m, 3H), 7.64 (d, 1H, J=2.4 Hz), 7.34 (s, 1H), 7.21-7.30 (m, 2H), 3.34-3.42 (m, 4H), 2.74 (t, 2H, J=7.2 Hz), 1.78-1.88 (m, 5H), 1.44-1.53 (m, 2H), 1.25-1.39 (m, 2H), 0.88 (t, 3H, J=7.2 Hz).

Example 129
Syntehsis of 3-(4-{4-[3-(1-n-butyloxyethyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methylacrylic acid (B50)

1H-NMR(DMSO-d6) 13.01 (bs, 2H), 7.94-8.03 (m, 3H), 7.65 (d, 1H, J=2.7 Hz), 7.31-7.43 (m, 3H), 4.77-4.84 (m, 1H), 3.24-3.41 (m, 2H), 1.81 (s, 3H), 1.45-1.55 (m, 2H), 1.41(d, 3H, J=6.3 Hz), 1.29-1.37 (m, 2H), 0.83-0.88 (m, 3H).

Example 130
Syntehsis of 3-(4-{4-[3-(1,4-dibutyloxybutyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methylacrylic acid (B51)

1H-NMR(DMSO-d6) 13.02 (bs, 2H), 8.00-8.04 (m, 3H), 7.64 (d, 1H, J=2.4 Hz), 7.31-7.41 (m, 3H), 4.68 (t, 1H, J=6.2 Hz), 3.28-3.33 (m, 6H), 1.81 (d, 3H, J=1.8 Hz), 1.60-1.76 (m, 4H), 1.40-1.52 (m, 4H), 1.23-1.37 (m, 4H), 0.86 (t, 3H, J=7.2 Hz).

Example 131
Syntehsis of 3-(2,6-difluoro-4-{4-[2-fluoro-3-(3-n-hexyloxy-1-methyloxyproyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B152)

1H-NMR(DMSO-d6) 13.02 (bs, 2H), 8.01-8.06 (m, 2H), 7.97 (d, 1H, J=8.7 Hz), 7.65 (d, 1H, J=2.4 Hz), 7.31-7.40 (m, 3H), 4.71 (t, 1H, J=6.6 Hz), 3.26-3.36 (m, 4H), 3.18 (s, 3H), 1.87-2.00 (m, 2H), 1.81 (s, 3H), 1.39-1.54 (m, 2H), 1.20-1.32 (m, 6H), 0.85 (t, 3H, J=6.6 Hz).

Example 132
Syntehsis of 3-(2,6-difluoro-4-{4-[2-fluoro-3-(1-methyloxy-4-n-pentyloxybutyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B53)

1H-NMR(DMSO-d6) 13.02 (bs, 2H), 8.00-8.06 (m, 2H), 7.97 (d, 1H, J=8.4 Hz), 7.65 (d, 1H, J=2.1 Hz), 7.34-7.38 (m, 3H), 4.60 (t, 1H, J=5.7 Hz), 3.22-3.40 (m, 4H), 3.19 (s, 3H), 1.81(d, 3H, J=1.5 Hz), 1.66-1.85 (m, 2H), 1.38-1.64 (m, 4H), 1.21-1.29 (m, 4H), 0.84 (t, 3H, J=6.6 Hz).

Example 133
Syntehsis of 3-(2,6-difluoro-4-{4-[2-fluoro-3-(1-methyloxy-3,3-dimethylbutyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B54)

1H-NMR(DMSO-d6) 13.01 (bs, 2H), 7.94-8.03 (m, 3H), 7.66 (d, 1H, J=2.5 Hz), 7.30-7.41 (m, 3H), 4.65 (dd, 1H, J=8.8 Hz, 3.0 Hz), 3.15 (s, 3H), 1.81 (d, 3H, J=1.6 Hz), 1.73 (dd, 1H, J=14.4 Hz, 8.6 Hz), 1.45 (dd, 1H, J=14.4 Hz, 2.8 Hz), 0.97 (s, 9H).

Example 134
Syntehsis of 3-(2,6-difluoro-4-{4-[2-fluoro-3-(1-methyloxy-3-n-butyloxypropyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B55)

1H-NMR(DMSO-d6) 13.02 (bs, 2H), 7.94-8.06 (m, 3H), 7.66 (d, 1H, J=2.7 Hz), 7.35-7.41 (m, 3H), 4.68-4.73 (m, 1H), 3.34-3.54 (m, 4H), 3.19 (s, 3H), 1.85-2.01 (m, 2H), 1.81 (d, 3H, J=1.6 Hz), 1.41-1.50 (m, 2H), 1.25-1.37 (m, 2H), 086 (t, 3H, J=7.2 Hz).

Example 135
Syntehsis of 3-(2,6-dichloro-4-{4-[3-(1-ethyloxy-2,2-dimethylpropyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B56)

1H-NMR(DMSO-d6) 13.02 (bs, 2H), 8.29 (s, 2H), 8.02 (m, 1H), 7.62 (d, 1H, J=2.3 Hz), 7.41 (s, 1H), 7.30-7.40 (m, 2H), 4.42 (s, 1H), 3.20-3.40 (m, 2H), 1.69 (s, 3H), 1.11 (t, 3H, J=7.0 Hz), 0.91 (s, 9H).

Example 136
Syntehsis of 3-(2,6-dichloro-4-{4-[2-fluoro-3-(4-methyloxy-4-heptyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B57)

1H-NMR(DMSO-d6) 13.02 (bs, 2H), 8.29 (s, 2H), 7.98 (t, 1H, J=7.3 Hz), 7.62 (d, 1H, J=2.4 Hz), 7.51 (t, 1H, J=7.0 Hz), 7.40 (d, 1H, J=1.2 Hz), 7.27 (t, 1H, J=7.8 Hz), 3.17 (s, 3H), 1.80-2.00 (m, 4H), 1.69 (d, 3H, J=1.2 Hz), 0.75-1.35 (m, 10H).

Example 137
Syntehsis of 3-(2,6-dichloro-4-{4-[2-fluoro-3-(1-methyloxyhexyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B58)

1H-NMR(DMSO-d6) 13.02(bs, 2H), 8.29 (s, 2H), 8.02 (m, 1H), 7.65 (d, 1H, J=2.5 Hz), 7.30-7.44 (m, 3H), 4.57 (t, 1H, J=6.8 Hz), 3.18 (s, 3H), 1.69 (d, 3H, J=1.1 Hz), 1.20-1.83 (m, 8H), 0.84 (t, 3H, J=6.1 Hz).

Example 138
Syntehsis of 3-(2,6-dichloro-4-{4-[2-fluoro-3-(3-methyloxy-2,4-dimethylpentyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B59)

1H-NMR(DMSO-d6) 13.00 (bs, 2H), 8.30 (s, 2H), 8.03 (m, 1H), 7.56 (d, 1H, J=3.1 Hz), 7.30-7.44 (m, 3H), 3.33 (s, 3H), 2.50-2.70 (m, 2H), 1.69 (d, 3H, J=1.2 Hz), 0.90 (d, 12H, J=6.7 Hz).

Example 139
Syntehsis of 3-(2,6-dichloro-4-{4-[2-fluoro-3-(1-methyloxy-4-methylpentyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B60)

1H-NMR(DMSO-d6) 13.03 (bs, 2H), 8.29 (d, 2H, J=1.2 Hz), 8.03 (m, 1H), 7.66 (d, 1H, J=0.9 Hz), 7.31-7.45 (m, 3H), 4.55 (t, 1H, J=6.3 Hz), 3.18 (d, 3H, J=1.2 Hz), 1.69 (s, 3H), 1.10-1.85 (m, 5H), 0.85 (d, 6H, J=6.7 Hz).

Example 140
Syntehsis of 3-(2,6-dichloro-4-{4-[2-fluoro-3-(1-methyloxydecyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B61)

1H-NMR(DMSO-d6) 13.03 (bs, 2H), 8.29 (s, 2H), 8.02 (m, 1H), 7.64 (d, 1H, J=1.5 Hz), 7.29-7.45 (m, 3H), 4.56 (t, 1H, J=6.4 Hz), 3.18 (s, 3H), 1.69 (s, 3H), 1.15-1.85 (m, 16H), 0.83 (t, 3H, J=6.6 Hz).

Example 141
Syntehsis of 3-(2,6-dichloro-4-{4-[2-fluoro-3-(1-ethyloxy-3,3-dimethylbutyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B62)

1H-NMR(DMSO-d6) 13.02 (bs, 2H), 8.29 (s, 2H), 8.00 (dt, 1H, J=1.8, 7.6 Hz), 7.65 (d, 1H, J=2.4 Hz), 7.29-7.45 (m, 3H), 4.77 (dd, 1H, J=2.4, 8.8 Hz), 3.25-3.40 (m, 2H), 1.69 (s, 3H), 1.68 (m, 1H), 1.43 (dd, 1H, J=2.4, 14.3 Hz), 1.12 (t, 3H, J=6.9 Hz), 0.99 (s, 9H).

Example 142
Syntehsis of 3-(2,6-dichloro-4-{4-[2-fluoro-3-(3-methyloxy-1-n-pentyloxypropyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B63)

1H-NMR(DMSO-d6) 13.01 (bs, 2H), 8.35 (s, 1H), 8.16 (d, 1H, J=9.9 Hz), 8.00-8.08 (m, 3H), 7.65 (d, 1H, J=2.4 Hz), 7.31-7.42 (m, 2H), 4.82 (q, 1H, J=4.2 Hz), 3.10-3.50 (m, 2H), 2.58 (t, 2H, J=7.5 Hz), 2.06(s, 3H), 1.82-2.02 (m, 2H), 1.46-1.58 (m, 2H), 1.20-1.36 (m, 4H), 0.85 (t, 3H, J=6.9 Hz).

Example 143
Syntehsis of 3-(2,6-dichloro-4-{4-[2-fluoro-3-(1-methyloxy-2,2-dimethylpropyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B64)

1H-NMR(DMSO-d6) 13.00 (bs, 2H), 8.29 (s, 2H), 8.03 (dt, 1H, J=7.0 Hz, 2.2 Hz), 7.62 (d, 1H, J=2.5 Hz), 7.28-7.41 (m, 3H), 4.32 (s, 1H), 3.15 (s, 3H), 1.69 (d, 3H, J=1.3 Hz), 0.91 (s, 9H).

Example 144
Syntehsis of 3-[2,6-dichloro-4-(4-{3-[1-(4-ethyloxybutyloxy)propyl]-2-fluorophenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B65)

1H-NMR(DMSO-d6) 13.03 (bs, 2H), 8.29 (s, 2H), 8.01 (t, 1H, J=6.0 Hz), 7.64 (d, 1H, J=2.1 Hz), 7.40 (s, 1H), 7.30-7.37 (m, 2H), 4.59 (t, 1H, J=6.0 Hz), 3.00-3.70 (m, 6H), 1.60-1.86 (m, 2H), 1.69 (s, 3H), 1.41-1.63 (m, 4H), 1.07 (t, 3H, J=6.9 Hz), 0.89 (t, 3H, J=6.9 Hz).

Example 145
Syntehsis of 3-[2,6-dichloro-4-(4-{3-[3-(2,2-dimethylpropyloxy)propyl]-2-fluorophenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B66)

1H-NMR(DMSO-d6) 13.01 (bs, 2H), 8.29 (s, 2H), 7.94 (dt, 1H, J=2.4 Hz, 7.2 Hz), 7.63 (d, 1H, J=2.7 Hz), 7.40 (d, 1H, J=1.5 Hz), 7.21-7.32 (m, 2H), 3.42 (t, 2H, J=6.0 Hz), 3.04 (s, 2H), 2.76 (t, 2H, J=7.2 Hz), 1.80-1.91 (m, 2H), 1.69 (d, 3H, J=1.2 Hz), 0.89 (s, 9H).

Example 146
Syntehsis of 3-[2,6-dichloro-4-(4-{3-[1-n-pentyloxypropyl]-2-fluorophenyl}thiazol-2-ylcarbamoyl)phenyl]-2-methylacrylic acid (B67)

1H-NMR(DMSO-d6) 13.02 (bs, 2H), 8.29 (s, 2H), 8.01 (dt, 1H, J=2.4 Hz, 6.9 Hz), 7.64 (d, 1H, J=2.4 Hz), 7.31-7.40 (m, 3H), 4.59 (t, 1H, J=6.9 Hz), 3.20-3.42 (m, 2H), 1.69 (d, 3H, J=1.5 Hz), 1.64-1.81 (m, 2H), 1.46-1.56 (m, 2H), 1.23-1.34 (m, 4H), 0.89 (t, 3H, J=7.2 Hz), 0.85 (t, 3H, J=7.2 Hz).

Example 147
Syntehsis of 3-(2,6-dichloro-4-{4-[2-fluoro-3-(1-methyloxyheptyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B68)

1H-NMR(DMSO-d6) 13.01 (bs, 1H), 8.29(d, 2H, J=0.9 Hz), 8.03 (t, 1H, J=7.3), 7.64 (d, 1H, J=2.3 Hz), 7.31-7.40 (m, 3H), 4.56 (t, 1H, J=6.5 Hz), 3.18 (s, 3H), 1.60-1.80 (m, 4H), 1.70 (d, 3H, J=1.3 Hz), 1.20-1.30 (m, 6H), 0.81-0.85 (m, 3H).

Example 148
Syntehsis of 3-(2,6-dichloro-4-{4-[2-fluoro-3-(1-methyloxyoctyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B69)

1H-NMR(DMSO-d6) 13.00(bs, 2H), 8.29 (d, 2H, J=0.9 Hz), 7.99-8.10 (m, 1H), 7.64 (d, 1H, J=1.3 Hz), 7.31-7.40 (m, 3H), 4.56 (t, 1H, J=6.5 Hz), 3.18 (s, 3H), 1.69 (d, 3H, J=1.3 Hz), 1.58-1.84 (m, 2H), 1.16-1.40 (m, 10H), 0.81-0.85 (m, 3H).

Example 149
Syntehsis of 3-(2,6-dichloro-4-{4-[2-fluoro-3-(1-n-pentyloxypentyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B70)

1H-NMR(DMSO-d6) 13.00 (bs, 2H), 8.29 (s, 2H), 8.00 (dt, 1H, J=7.4 Hz, 2.2 Hz), 7.64 (d, 1H, J=2.5 Hz), 7.30-7.40 (m, 3H), 4.64 (dt, 1H, J=1.6 Hz, 5.5 Hz), 3.28 (t, 2H, J=6.6 Hz), 1.69 (d, 3H, J=1.3 Hz), 1.62-1.73 (m, 2H), 1.45-1.52 (m, 2H), 1.22-1.33 (m, 8H), 0.82-0.87 (m, 6H).

Example 150
Syntehsis of 3-(2,6-dichloro-4-{4-[3-(1-ethyloxypentyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B71)

1H-NMR(DMSO-d6) 13.00 (bs, 2H), 8.29 (s, 1H), 8.00 (dt, 1H, J=7.3 Hz, 2.0 Hz), 7.64 (d, 1H, J=2.5 Hz), 7.30-7.40 (m, 3H), 4.67 (t, 1H, J=6.6 Hz), 3.35 (q, 2H, J=6.9 Hz), 1.63-1.73 (m, 5H), 1.27-1.33 (m, 4H), 1.12 (t, 3H, J=6.9 Hz), 0.83-0.87 (m, 3H).

Example 151
Syntehsis of 3-(2,6-dichloro-4-{4-[2-fluoro-3-(1-methyloxynonyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B72)

1H-NMR(DMSO-d6) 13.02 (bs, 2H), 8.29 (s, 2H), 8.01 (m, 1H), 7.65 (d, 1H, J=2.4 Hz), 7.41 (d, 1H, J=1.2 Hz), 7.32-7.38 (m, 2H), 4.52 (t, 1H, J=6.6 Hz), 3.20 (s, 3H), 1.68-1.84 (m, 5H), 1.18-1.40 (m, 12H), 0.87 (t, 3H, J=7.2 Hz).

Example 152
Syntehsis of 3-(2,6-dichloro-4-{4-[2-fluoro-3-(3-methyloxyoctyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B73)

1H-NMR(DMSO-d6) 13.02 (bs, 2H), 8.29 (s, 2H), 7.93 (dt, 1H, J=1.8 Hz, 7.5 Hz), 7.64 (d, 1H, J=2.7 Hz), 7.40 (d, 1H, J=1.2 Hz), 7.20-7.31 (m, 2H), 3.25 (s, 3H), 3.19 (m, 1H), 2.62-2.80 (m, 2H), 1.72-1.77 (m, 2H), 1.69 (d, 3H, J=1.2 Hz), 1.40-1.54 (m, 2H), 1.20-1.38 (m, 6H), 0.86 (t, 3H, J=6.6 Hz).

Example 153
Syntehsis of 3-[2,6-dichloro-4-(4-{2-fluoro-3-[1-(3-methylbutyloxy)proptyl]phenyl}thiazol-2-ylcarbamoyl)phenyl]-2-methylacrylic acid (B74)

1H-NMR(DMSO-d6) 13.01 (bs, 2H), 8.29 (s, 2H), 8.01 (dt, 1H, J=2.4 Hz, 6.9 Hz), 7.64 (d, 1H, J=2.7 Hz), 7.40 (t, 1H, J=1.5 Hz), 7.31-7.38 (m, 2H), 4.59 (t, 1H, J=6.0 Hz), 3.12-3.43 (m, 2H), 1.63-1.81 (m, 3H), 1.37-1.44 (m, 2H), 0.89 (t, 3H, J=7.2 Hz), 0.86 (t, 3H, J=6.6 Hz), 0.82 (t, 3H, J=6.6 Hz).

Example 154
Syntehsis of 3-(2,6-dichloro-4-{4-[2-fluoro-3-(1-n-octyloxyethyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B75)

1H-NMR(DMSO-d6) 13.00 (bs, 2H), 8.29 (s, 2H), 8.01 (dt, 1H, J=7.5 Hz, 2.0 Hz), 7.64 (d, 1H, J=2.7 Hz), 7.38-7.42 (m, 1H), 7.32 (t, 2H, J=7.7 Hz), 4.79 (q, 1H, J=6.7 Hz), 3.23-3.40 (m, 2H), 1.69 (s, 3H), 1.45-1.40 (m, 2H), 1.41 (d, 3H, 6.4 Hz), 1.22-1.30 (m, 8H), 0.81-0.86 (m, 3H).

Example 155
Syntehsis of 3-{2,6-dichloro-4-[4-(3-n-decyloxymethyl-2-fluorophenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methylacrylic acid (B76)

1H-NMR(DMSO-d6) 13.03 (bs, 2H), 8.29 (s, 2H), 8.04 (dt, 1H, J=7.7 Hz, 1.3 Hz), 7.64 (d, 1H, J=2.5 Hz), 7.38-7.45 (m, 2H), 7.31 (t, 1H, J=7.7 Hz), 4.58 (s, 2H), 3.48 (t, 2H, 6.5 Hz), 1.69 (s, 3H), 1.49-1.58 (m, 2H), 1.22-1.33 (m, 14H), 0.82-0.86 (m, 3H).

Example 156
Syntehsis of 3-{2,6-dichloro-4-[4-(2-fluoro-3-{n-pentyloxymethyl}phenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methylacrylic acid (B77)

1H-NMR(DMSO-d6) 13.02 (bs, 2H), 8.29 (s, 2H), 8.04 (dt, 1H, J=7.5 Hz, 1.8 Hz), 7.66 (d, 1H, J=2.4 Hz), 7.40-7.46 (m, 2H), 7.31 (t, 1H, J=7.6 Hz), 4.58 (s, 2H), 3.49 (t, 2H, 6.4 Hz), 1.69 (d, 3H, J=1.5 Hz), 1.52-1.60 (m, 2H), 1.28-1.33 (m, 4H), 0.84-0.89 (m, 3H).

Example 157
Syntehsis of 3-(2,6-dichloro-4-{4-[2-fluoro-3-(1-n-propyloxybutyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B78)

1H-NMR(DMSO-d6) 13.01 (bs, 1H), 8.29 (d, 2H, J=0.9 Hz), 8.03 (t, 1H, J=7.3), 7.64 (d, 1H, J=2.3 Hz), 7.31-7.40 (m, 3H), 4.67 (t, 1H, J=6.5 Hz), 3.21 (t, 2H, J=6.5), 1.66 (d, 3H, J=1.3 Hz), 1.30-1.84 (m, 6H), 0.81-0.85 (m, 6H).

Example 158
Syntehsis of 3-(4-{4-[3-(1-n-butyloxybutyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}-2,6-dichlorophenyl)-2-methylacrylic acid (B79)

1H-NMR(DMSO-d6) 13.00 (bs, 1H), 8.27 (d, 2H, J=0.9 Hz), 8.00 (t, 1H, J=7.4), 7.63 (d, 1H, J=2.3 Hz), 7.31-7.38 (m, 3H), 4.67 (t, 1H, J=6.4 Hz), 3.21 (t, 2H, J=6.5), 1.69 (d, 3H, J=1.3 Hz), 1.20-1.84 (m, 8H), 0.81-0.85 (m, 6H).

Example 159
Syntehsis of 3-(2,6-dichloro-4-{4-[2-fluoro-3-(1-n-pentyloxybutyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B80)

1H-NMR(DMSO-d6) 13.00 (bs, 1H), 8.28 (d, 2H, J=0.9 Hz), 8.00 (t, 1H, J=7.4), 7.63 (d, 1H, J=2.3 Hz), 7.31-7.38 (m, 3H), 4.65 (t, 1H, J=6.4 Hz), 3.21 (t, 2H, J=6.5), 1.70 (d, 3H, J=1.3 Hz), 1.20-1.70 (m, 10H), 0.81-0.85 (m, 6H).

Example 160
Syntehsis of 3-(2,6-dichloro-4-{4-[2-fluoro-3-(1-n-propyloxypropyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B81)

1H-NMR(DMSO-d6) 13.02 (bs, 2H), 8.29 (s, 2H), 8.01 (dt, 1H, J=2.1 Hz, 7.2 Hz), 7.64 (d, 1H, J=2.4 Hz), 7.31-7.43 (m, 3H), 4.60 (t, 1H, J=6.3 Hz), 3.21-3.40 (m, 3H), 1.69 (d, 3H, J=1.2 Hz), 1.64-1.82 (m, 2H), 1.47-1.59 (m, 2H), 0.89 (t, 3H, J=7.5 Hz), 0.88 (t, 3H, J=7.2 Hz).

Example 161
Syntehsis of 3-(4-{4-[3-(1-n-butyloxypropyl)-2-fluorophenyl]hiazol-2-ylcarbamoyl}-2,6-dichlorophenyl)-2-methylacrylic acid (B82)

1H-NMR(DMSO-d6) 13.02 (bs, 2H), 8.29 (s, 2H), 8.01 (dt, 1H, J=2.1 Hz, 7.2 Hz), 7.64 (d, 1H, J=2.7 Hz), 7.40 (d, 1H, J=1.5 Hz), 7.31-7.38 (m, 2H), 4.59 (t, 1H, J=6.6 Hz), 3.24-0.37 (m, 2H), 1.69 (d, 3H, J=1.2 Hz), 1.45-1.55 (m, 2H), 1.28-1.40 (m, 4H), 0.89 (t, 3H, J=7.5 Hz), 0.86 (t, 3H, J=7.2 Hz).

Example 162
Syntehsis of 3-(2,6-dichloro-4-{4-[2-fluoro-3-(1-n-hexyloxypropyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B83)

1H-NMR(DMSO-d6) 13.02 (bs, 2H), 8.29 (s, 2H), 8.01 (dt, 1H, J=2.7 Hz, 6.9 Hz), 7.64 (d, 1H, J=2.7 Hz), 7.30-7.40 (m, 3H), 4.59 (t, 1H, J=6.6 Hz), 3.25-3.39 (m, 2H), 1.64-1.81 (m, 2H), 1.69 (d, 3H, J=1.2 Hz), 1.49-1.56 (m, 2H), 1.16-1.36 (m, 6H), 0.89 (t, 3H, J=7.2 Hz), 0.84 (t, 3H, J=6.6 Hz).

Example 163
Syntehsis of 3-[2,6-dichloro-4-(4-[2-fluoro-3-[3-(4-methylpentyloxy)propyl]phenyl]thiazol-2-ylcarbamoyl)phenyl]-2-methylacrylic acid (B84)

1H-NMR(DMSO-d6) 13.00 (bs, 2H), 8.29 (s, 2H), 7.94 (dt, 1H, J=2.4 Hz, 7.2 Hz), 7.63 (d, 1H, J=2.4 Hz), 7.40 (d, 1H, J=1.2 Hz), 7.21-7.30 (m, 2H), 3.32-3.41 (m, 4H), 2.74 (t, 2H, J=7.8 Hz), 1.78-1.88 (m, 2H), 1.69 (d, 3H, J=1.5 Hz), 1.45-1.56 (m, 3H), 1.14-1.22 (m, 2H), 0.86 (d, 6H, J=6.6 Hz).

Example 164
Syntehsis of 3-[2,6-dichloro-4-(4-[3-[3-(3,3-dimethylbutyloxy)propyl]-2-fluorophenyl]thiazol-2-ylcarbamoyl)phenyl]-2-methylacrylic acid (B85)

1H-NMR(DMSO-d6) 13.02 (bs, 2H), 8.29 (s, 2H), 7.94 (dt, 1H, J=1.8 Hz, 7.8 Hz), 7.63 (d, 1H, J=2.4 Hz), 7.41 (s, 1H), 7.21-7.30 (m, 2H), 3.25-3.48 (m, 4H), 2.74 (t, 2H, J=7.5 Hz), 1.78-1.87 (m, 2H), 1.69 (d, 3H, J=1.2 Hz), 1.44 (t, 2H, J=7.5 Hz), 0.90 (s, 9H).

Example 165
Syntehsis of 3-(2,6-dichloro-4-{4-[2-fluoro-3-(1-n-propyloxypentyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B86)

1H-NMR(DMSO-d6) 13.01 (bs, 2H), 8.29 (s, 2H), 8.00 (dt, 1H, J=7.5 Hz, 2.0 Hz), 7.64 (d, 1H, J=2.5 Hz), 7.30-7.41 (m, 3H), 4.63-4.67(m, 1H), 3.25 (t, 2H, 6.4 Hz), 1.64-1.78 (m, 5H), 1.52 (q, 2H, J=6.9 Hz), 1.28-1.33 (m, 4H), 0.84-0.90 (m, 6H).

Example 166
Syntehsis of 3-(4-{4-[3-(1-n-butyloxypentyl)-2-fluorophenyl]hiazol-2-ylcarbamoyl}-2,6-dichlorophenyl)-2-methylacrylic acid (B87)

1H-NMR(DMSO-d6) 13.01 (bs, 2H), 8.29 (s, 2H), 8.00 (dt, 1H, J=7.5 Hz, 2.2 Hz), 7.64-7.65 (m, 1H), 7.30-7.41 (m, 3H), 4.62-4.67(m, 1H), 3.29 (t, 2H, 6.4 Hz), 1.60-1.80 (m, 5H), 1.45-1.54 (m, 2H), 1.28-1.40 (m, 6H), 0.82-0.88 (m, 6H).

Example 167
Syntehsis of 3-[2,6-dichloro-4-(4-[3-[3-(2-ethylbutyloxy)propyl]-2-fluorophenyl]thiazol-2-ylcarbamoyl)phenyl]-2-methylacrylic acid (B88)

1H-NMR(DMSO-d6) 13.01 (bs, 2H), 8.29 (s, 2H), 7.94 (dt, 1H, J=2.4 Hz, 7.5 Hz), 7.63 (d, 1H, J=2.7 Hz), 7.40 (d, 1H, J=1.5 Hz), 7.21-7.30 (m, 2H), 3.40 (t, 2H, J=6.3 Hz), 3.26 (d, 2H, J=5.4 Hz), 2.74 (t, 2H, J=7.2 Hz), 1.74-1.91 (m, 2H), 1.69 (d, 3H, J=1.5 Hz), 1.20-1.42 (m, 5H), 0.85 (t, 6H, J=7.8 Hz).

Example 168
Syntehsis of 3-[2,6-dichloro-4-(4-[3-[3-(2-cyclopentylethyloxy)propyl]-2-fluorophenyl]thiazol-2-ylcarbamoyl)phenyl]-2-methylacrylic acid (B89)

1H-NMR(DMSO-d6) 13.01 (bs, 2H), 8.29 (s, 2H), 7.94 (dt, 1H, J=2.4 Hz, 7.2 Hz), 7.63 (d, 1H, J=2.7 Hz), 7.40 (d, 1H, J=1.5 Hz), 7.20-7.30 (m, 2H), 3.20-3.46 (m, 4H), 2.74 (t, 2H, J=7.8 Hz), 1.60-1.90 (m, 4H), 1.69 (d, 3H, J=1.5 Hz), 1.44-1.59 (m, 5H), 1.02-1.15 (m, 4H).

Example 169
Syntehsis of 3-(2,6-dichloro-4-{4-[2-fluoro-3-(3-n-pentyloxy)propyl]phenyl]thiazol-2-ylcarbamoyl)phenyl]-2-methylacrylic acid (B90)

1H-NMR(DMSO-d6) 13.01 (bs, 2H), 8.29 (s, 2H), 7.94 (dt, 1H, J=2.1 Hz, 6.6 Hz), 7.63 (d, 1H, J=2.4 Hz), 7.40 (s, 1H), 7.21-7.30 (m, 2H), 3.33-3.42 (m, 4H), 2.74 (t, 2H, J=7.5 Hz), 1.78-1.88 (m, 2H), 1.69 (d, 3H, J=1.2 Hz), 1.44-1.57 (m, 2H), 1.26-1.31 (m, 4H), 0.87 (t, 3H, J=7.2 Hz).

Example 170
Syntehsis of 3-(2,6-dichloro-4-{4-[2-fluoro-3-(1-methyloxyundecyl)phenyl]thiazol-2-ylcarbamoyl)phenyl]-2-methylacrylic acid (B91)

1H-NMR(DMSO-d6) 13.01 (bs, 2H), 8.29 (s, 2H), 7.99-8.05 (m, 1H), 7.64 (s, 1H), 7.30-7.40 (m, 3H), 4.56 (t, 1H, J=6.5 Hz), 3.18 (s, 3H), 1.60-1.80 (m, 5H), 1.14-1.36 (m, 16H), 0.81-0.85 (m, 3H).

Example 171
Syntehsis of 3-(2,6-dichloro-4-{4-[2-fluoro-3-(1-methyloxydodecyl)phenyl]thiazol-2-ylcarbamoyl)phenyl]-2-methylacrylic acid (B92)

1H-NMR(DMSO-d6) 13.01 (bs, 2H), 8.29 (s, 2H), 8.00-8.05 (m, 1H), 7.64 (d, 1H, J=2.7 Hz), 7.31-7.41 (m, 3H), 4.56 (t, 1H, J=6.4 Hz), 3.18 (s, 3H), 1.60-1.80 (m, 5H), 1.20-1.36 (m, 18H), 0.81-0.85 (m, 3H).

Example 172
Syntehsis of 3-(4-{4-[3-(3-n-butyloxypropyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}-2,6-dichlorophenyl]-2-methylacrylic acid (B93)

1H-NMR(DMSO-d6) 13.04 (bs, 2H), 8.29 (s, 2H), 7.94 (dt, 1H, J=2.4 Hz, 7.2 Hz), 7.64 (d, 1H, J=2.7 Hz), 7.40 (d, 1H, J=1.2 Hz), 7.21-7.32 (m, 2H), 3.20-3.42 (m, 4H), 2.74 (t, 2H, J=8.1 Hz), 1.78-1.88 (m, 2H), 1.69 (d, 3H, J=1.2 Hz), 1.44-1.53 (m, 2H), 1.27-1.39 (m, 2H), 0.88 (t, 3H, J=6.9 Hz).

Example 173
Syntehsis of 3-(2,6-dichloro-4-{4-[2-fluoro-3-(3-isopropyloxypropyl)phenyl]thiazol-2-ylcarbamoyl)phenyl]-2-methylacrylic acid (B94)

1H-NMR(DMSO-d6) 13.02 (bs, 2H), 8.29 (s, 2H), 7.94 (dt, 1H, J=2.4 Hz, 7.2 Hz), 7.64 (d, 1H, J=2.7 Hz), 7.41 (d, 1H, J=1.2 Hz), 7.21-7.31 (m, 2H), 3.52 (m, 1H), 3.35-3.41 (m, 2H), 2.74 (t, 2H, J=8.1 Hz), 1.76-1.85 (m, 2H), 1.69 (d, 3H, J=1.8 Hz), 1.09 (d, 6H, J=6.3 Hz).

Example 174
Syntehsis of 3-(2,6-dichloro-4-{4-[2-fluoro-3-(3-n-propyloxypropyl)phenyl]thiazol-2-ylcarbamoyl)phenyl]-2-methylacrylic acid (B95)

1H-NMR(DMSO-d6) 13.02 (bs, 2H), 8.29 (s, 2H), 7.94 (dt, 1H, J=1.8 Hz, 7.2 Hz), 7.64 (d, 1H, J=2.4 Hz), 7.41 (1, 1H), 7.21-7.31 (m, 2H), 3.30-3.42 (m, 4H), 2.74 (t, 2H, J=7.8 Hz), 1.78-1.88 (m, 2H), 1.69 (s, 3H), 1.49-1.58 (m, 2H), 0.88 (t, 3H, J=7.5 Hz).

Example 175
Syntehsis of 3-(2,6-dichloro-4-{4-[2-fluoro-3-(3-n-hexyloxypropyl)phenyl]thiazol-2-ylcarbamoyl)phenyl]-2-methylacrylic acid (B96)

1H-NMR(DMSO-d6) 13.02 (bs, 2H), 8.29 (s, 2H), 7.93 (dt, 1H, J=2.7 Hz, 7.8 Hz), 7.63 (d, 1H, J=2.4 Hz), 7.41 (d, 1H, J=1.5 Hz), 7.21-7.31 (m, 2H), 3.20-3.45 (m, 4H), 2.74 (t, 2H, J=7.5 Hz), 1.78-1.87 (m, 2H), 1.69 (d, 3H, J=1.8 Hz), 1.44-1.53 (m, 2H), 1.21-1.36 (m, 6H), 0.86 (t, 3H, J=6.9 Hz).

Example 176
Syntehsis of 3-(2,6-dichloro-4-{4-[2-fluoro-3-(1-n-propyloxyethyl)phenyl]thiazol-2-ylcarbamoyl)phenyl]-2-methylacrylic acid (B97)

1H-NMR(DMSO-d6) 13.01 (bs, 2H), 8.29 (s, 2H), 8.01 (dt, 1H, J=7.6 Hz, 1.8 Hz), 7.65 (d, 1H, J=2.4 Hz), 7.31-7.45 (m, 3H), 4.80 (t, 1H, J=6.4 Hz), 3.20-3.39 (m, 2H), 1.69 (d, 3H, J=1.5 Hz), 1.52 (qint, 2H, J=7.0 Hz), 1.41(d, 3H, J=6.4 Hz), 0.87 (t, 3H, J=7.3 Hz).

Example 177
Syntehsis of 3-(4-{4-[3-(1-n-butyloxyethyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl)-2,6-dichlorophenyl]-2-methylacrylic acid (B98)

1H-NMR(DMSO-d6) 13.01 (bs, 2H), 8.29 (s, 2H), 8.01 (dt, 1H, J=7.3 Hz, 1.8 Hz), 7.65 (d, 1H, J=2.4 Hz), 7.39-7.44 (m, 1H), 7.34 (t, 2H, J=7.6 Hz), 4.80 (q, 1H, J=6.4 Hz), 3.25-3.41 (m, 2H), 1.69 (d, 3H, J=1.2 Hz), 1.45-1.55 (m, 2H), 1.41(d, 3H, J=6.4 Hz), 1.29-1.37 (m, 2H), 0.86 (t, 3H, J=7.3 Hz).

Example 178
Syntehsis of 3-(2,6-dichloro-4-{4-[2-fluoro-3-(1-n-hexyloxyethyl)phenyl]thiazol-2-ylcarbamoyl)phenyl]-2-methylacrylic acid (B99)

1H-NMR(DMSO-d6) 13.02 (bs, 2H), 8.29 (s, 2H), 8.00 (dt, 1H, J=7.5 Hz, 1.9 Hz), 7.64 (d, 1H, J=2.5 Hz), 7.31-7.43 (m, 3H), 4.80 (q, 1H, J=6.4 Hz), 3.23-3.40 (m, 2H), 1.69 (d, 3H, J=1.4 Hz), 1.46-1.53 (m, 2H), 1.41(d, 3H, J=6.4 Hz), 1.20-1.35 (m, 6H), 0.82-0.87 (m, 3H).

Example 179
Syntehsis of 3-(4-{4-[3-(1,4-dibutyloxybutyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl)-2,6-dichlorophenyl]-2-methylacrylic acid (B100)

1H-NMR(DMSO-d6) 13.02 (bs, 2H), 8.29 (s, 2H), 8.01 (dt, 1H, J=2.1 Hz, 6.8 Hz), 7.64 (d, 1H, J=2.4 Hz), 7.41 (d, 1H, J=1.5 Hz), 7.31-7.38 (m, 2H), 4.68 (t, 3H, J=6.2 Hz), 3.16-3.20 (m, 6H), 1.69 (d, 3H, J=1.5 Hz), 1.55-1.75 (m, 4H), 1.40-1.54 (m, 4H), 1.25-1.37 (m, 4H), 0.85 (dt, 6H, J=1.2 Hz,6.9 Hz).

Example 180
Syntehsis of 3-(2,6-dichloro-4-{4-[2-fluoro-3-(3-n-hexyloxy-1-methyloxypropyl)phenyl]thiazol-2-ylcarbamoyl)phenyl]-2-methylacrylic acid (B101)

1H-NMR(DMSO-d6) 13.02 (bs, 2H), 8.29 (s, 2H), 8.03 (dt, 1H, J=2.1 Hz, 6.6 Hz), 7.65 (d, 1H, J=2.7 Hz), 7.32-7.41 (m, 3H), 4.71 (m, 1H,), 3.25-3.40 (m, 4H), 3.18 (s, 3H), 1.83-2.01 (m, 2H), 1.69 (s, 3H), 1.40-1.50 (m, 2H), 1.18-1.32 (m, 6H), 0.85 (t, 3H, J=6.9 Hz).

Example 181
Syntehsis of (Z)-3-(4-{4-[3-(4-methylpentyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl)phenyl]-2-methyloxyacrylic acid (B121)

1H-NMR(DMSO-d6) 13.56 (bs, 1H), 12.96 (bs, 1H), 7.89-7.96 (m, 3H), 7.63 (d, 1H, J=2.6 Hz), 7.20-7.31 (m, 2H), 6.66 (s, 1H), 3.71 (s, 3H), 2.67 (t, 2H, J=7.6 Hz), 1.53-1.62 (m, 3H), 1.20-1.27 (m, 2H), 0.88 (d, 6H, J=6.6 Hz).

Example 182
Syntehsis of (Z)-3-(4-{4-[3-(3,3-dimethylbutyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl]-2-methyloxyacrylic acid (B122)

1H-NMR(DMSO-d6) 13.01 (bs, 2H), 8.29 (s, 2H), 8.00-8.06 (m, 1H), 7.65 (d, 1H, J=2.6 Hz), 7.31-7.41 (m, 3H), 4.69-4.74 (m, 1H), 3.48-3.55 (m, 1H), 3.25-3.40 (m, 3H), 1.86-2.03 (m, 2H), 1.69(s,3H), 1.43-1.54 (m, 2H), 0.83-0.88 (m, 3H).

Example 183
Syntehsis of (E)-3-(4-{4-[3-(3,3-dimethylbutyl)-2-methyoxyphenyl]thiazol-2-ylcarbamoyl)-2,6-difluorophenyl]-2-methylacrylic acid (B134)

1H-NMR(DMSO-d6) 12.98(bs, 2H), 7.92-8.00(m, 2H), 7.84(dd, 1H, J=1.8, 6.9 Hz), 7.72(s, 1H), 7.33(s, 1H), 7.12-7.23(m, 2H), 3.62(s, 3H), 2.60-2.65(m, 2H), 1.81(s, 3H), 1.45-1.51(m, 2H), 0.98(s, 9H).

Example 184
Syntehsis of (Z)-3-(2,6-dichloro-4-{4-[2-fluoro-3-(4-methylpentyl)phenyl]thiazol-2-ylcarbamoyl)phenyl]-2-methyloxyacrylic acid (B169)

1H-NMR(DMSO-d6) 13.20 (bs, 1H), 12.99 (bs, 1H), 8.25 (s, 2H), 7.90-7.96 (m, 1H), 7.62-7.63 (m, 1H), 7.20-7.30 (m, 2H), 6.73 (s, 1H), 3.61 (s, 3H), 2.67 (t, 2H, J=7.6 Hz), 1.53-1.66 (m, 3H), 1.20-1.27 (m, 2H), 0.88 (d, 6H, J=6.6 Hz).

Example 185
Syntehsis of (Z)-3-(2,6-dichloro-4-{4-[3-(3,3-dimethylbutyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl)phenyl]-2-methyloxyacrylic acid (B170)

1H-NMR(DMSO-d6) 13.51 (bs, 1H), 13.00 (bs, 1H), 8.25 (s, 2H), 7.89-7.95 (m, 1H), 7.63 (d, 1H, J=2.6 Hz), 7.19-7.31 (m, 2H), 6.73 (s, 1H), 3.62 (s, 3H), 2.62-2.68 (m, 2H), 1.45-1.50 (m, 2H), 0.97 (s, 9H).

Example 186
Syntehsis of (E)-3-(2,6-difluoro-4-{4-[2-fluoro-3-(1-methyloxypropyl)phenyl]thiazol-2-ylcarbamoyl)phenyl]-2-methylacrylic acid (B195)

1H-NMR(DMSO-d6) 12.98(bs, 2H), 7.92-8.08(m, 3H), 7.65(d, 1H, J=2.7 Hz), 7.30-7.41(m, 3H), 4.52(t, 1H, J=6.3 Hz), 3.20(s, 3H), 1.65-1.85(m, 5H), 0.87(t, 3H, J=7.2 Hz).

Example 187
Syntehsis of (E)-3-(2,6-difluoro-4-{4-[2-fluoro-3-(1-propyloxypropyl)phenyl]thiazol-2-ylcarbamoyl)phenyl]-2-methylacrylic acid (B216)

1H-NMR(DMSO-d6) 13.00(bs, 2H), 7.92-8.05(m, 3H), 7.64(d, 1H, J=2.7 Hz), 7.30-7.42(m, 3H), 4.60(t, 1H, J=6.6 Hz), 3.10-3.42(m, 2H), 1.65-1.86(m, 5H), 1.47-1.59(m, 2H), 0.85-0.92(m, 6H).

Example 188
Syntehsis of (E)-3-(4-{4-[3-(cyclohexylpropyloxymethyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methylacrylic acid (B233)

1H-NMR(DMSO-d6) 13.00 (bs, 2H), 7.95-8.04 (m, 3H), 7.64 (d, 1H, J=2.6 Hz), 7.32-7.35 (m, 3H), 4.40 (d, 1H, J=7.0 Hz), 3.17-3.23 (m, 2H), 1.93-1.97 (m, 1H), 1.04-1.64 (m, 12H), 0.86 (t, 3H, J=7.5 Hz).

Example 189
Syntehsis of (E)-3-(4-{4-[3-(1-butyloxy-2,2-dimethylpropyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methylacrylic acid (B255)

1H-NMR(DMSO-d6) 12.99 (bs, 2H), 7.95-8.05 (m, 3H), 7.61-7.62 (m, 1H), 7.32-7.34 (m, 3H), 4.39 (s, 1H), 3.22 (t, 2H, J=6.3 Hz), 1.81 (s, 3H), 1.33-1.51 (m, 4H), 0.84-0.91 (m, 12H).

Example 190
Syntehsis of (E)-3-(4-{4-[3-(butyloxycyclohexylmethyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methylacrylic acid (B264)

1H-NMR(DMSO-d6) 13.00 (bs, 2H), 7.94-8.04 (m, 3H), 7.64 (d, 1H, J=2.6 Hz), 7.32-7.34 (m, 3H), 4.39 (d, 1H, J=7.0 Hz), 3.22-3.27 (m, 2H), 1.93-1.97 (m, 1H), 1.04-1.64 (m, 14H), 0.86 (t, 3H, J=7.5 Hz).

Example 191
Syntehsis of (E)-3-(2,6-difluoro-4-{4-[2-methyloxy-3-(1-methyloxyhexyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B347)

1H-NMR(DMSO-d6) 13.00(bs, 2H), 7.90-8.00(m, 3H), 7.72(s, 1H), 7.24-7.45(m, 3H), 4.56-4.60(m, 1H), 3.62(s, 3H), 3.16(s, 3H), 1.81(s, 3H), 1.20-1.78(m, 8H), 0.83-0.88(m, 3H).

Example 192
Syntehsis of (E)-3-(2,6-difluoro-4-{4-[2-methyloxy-3-(1-methyloxy-5-methylhexyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B348)

1H-NMR(DMSO-d6) 12.97 (bs, 2H), 7.89-7.97 (m, 3H), 7.72 (s, 1H), 7.24-7.34 (m, 3H), 4.53-4.57 (m, 1H), 3.61 (s, 3H), 3.16 (s, 3H), 1.81 (s, 3H), 0.87-1.72 (m, 13H).

Example 193
Syntehsis of (E)-3-(2,6-difluoro-4-{4-[2-methyloxy-3-(1-methyloxy-3,3-dimethylbutyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B349)

1H-NMR(DMSO-d6) 12.98(bs, 2H), 7.92-8.00(m, 2H), 7.89(dd, 1H, J=1.8, 7.5 Hz), 7.71(s, 1H), 7.31-7.36(m, 2H), 7.25(t, 1H, J=7.8 Hz), 4.69(d, 1H, J=7.8 Hz), 3.63(s, 3H), 3.13(s, 3H), 1.81(s, 3H), 1.63-1.71(m, 1H), 1.40(d, 1H, J=14.4 Hz), 1.00(s, 9H).

Example 194
Syntehsis of (E)-3-(2,6-difluoro-4-{4-[2-methyloxy-3-(1-methyloxydecyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B354)

1H-NMR(DMSO-d6) 13.00(bs, 2H), 7.90-8.00(m, 3H), 7.72(s, 1H), 7.24-7.36(m, 3H), 4.554.59(m, 1H), 3.61(s, 3H), 3.16(s, 3H), 1.81(s, 3H), 1.50-1.78(m, 2H), 1.16-1.50(m, 14H), 0.82-0.87(m, 3H).

Example 195
Syntehsis of (E)-3-(2,6-difluoro-4-{4-[2-methyloxy-3-(1-methyloxyundecyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B355)

1H-NMR(DMSO-d6) 13.00(bs, 2H), 7.90-8.00(m, 3H), 7.73(s, 1H), 7.24-7.36(m, 3H), 4.56-4.59(m, 1H), 3.61(s, 3H), 3.15(s, 3H), 1.81(s, 3H), 1.50-1.78(m, 2H), 1.16-1.50(m, 16H), 0.82-0.87(m, 3H).

Example 196
Syntehsis of (E)-3-(2,6-difluoro-4-{4-[2-methyloxy-3-(3-propyloxypropyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B380)

1H-NMR(CDCl3-d6) 7.90(s, 1H), 7.87(s, 1H), 7.58(s, 1H), 7.48-7.52(m, 1H), 7.46(s, 1H), 7.25-7.30(m, 1H), 7.18(t, 1H, J=7.5 Hz), 3.58(s, 3H), 3.50(t, 2H, J=6.3 Hz), 3.41(t, 2H, J=6.6 Hz), 2.80(t, 2H, J=8.4 Hz), 1.91-2.02(m, 5H), 1.63(q, 2H, J=7.2 Hz), 0.95 (t, 3H, J=7.5 Hz).

Example 197
Syntehsis of (E)-3-(4-{4-[3-(cyclohexylpropyloxymethyl-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methylacrylic acid (B397)

1H-NMR(DMSO-d6) 12.98(bs, 2H), 7.92-8.00(m, 2H), 7.89(dd, 1H, J=1.8, 6.9 Hz), 7.71(s, 1H), 7.34(s, 1H), 7.22-7.31(m, 2H), 4.40(d, 1H, J=6.9 Hz), 3.59(s, 3H), 3.06-3.25(m, 2H), 1.90-2.00(m, 1H), 1.81(s, 3H), 1.44-1.76(m, 6H), 1.36-1.28(m, 1H), 1.00-1.20(m, 5H), 0.87(t, 3H, J=7.2 Hz).

Example 198
Syntehsis of (E)-3-(4-{4-[3-(1-butyloxypropyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methylacrylic acid (B418)

1H-NMR(DMSO-d6) 12.99(bs, 2H), 7.89-8.05(m, 3H), 7.72(s, 1H), 7.31-7.36(m, 2H), 7.26(t, 1H, J=7.8 Hz), 4.55-4.63(m, 1H), 3.61(s, 3H), 1.81(s, 3H), 1.62-1.76(m, 2H), 1.43-1.55(m, 2H), 1.28-1.41(m, 2H), 0.84-0.95(m, 6H).

Example 199
Syntehsis of (E)-3-(4-{4-[3-(3-butyloxypropyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methylacrylic acid (B419)

1H-NMR(CDCl3-d6) 7.91(s, 1H), 7.88(s, 1H), 7.58(s, 1H), 7.49(d, 1H, J=7.5 Hz), 7.46(s, 1H), 7.25-7.29(m, 1H), 7.17(t, 1H, J=7.8 Hz), 3.58(s, 3H), 3.50(t, 1H, J=6.6 Hz), 3.45(t, 1H, J=6.9 Hz), 2.80(t, 2H, J=8.4 Hz), 1.90-2.02(m, 5H), 1.53-1.64(m, 2H), 1.34-1.48(m, 2H), 0.94(t, 3H, J=7.2 Hz).

Example 200
Syntehsis of (E)-3-(4-{4-[3-(1-butyloxy-2,2-dimethylpropyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methylacrylic acid (B425)

1H-NMR(DMSO-d6) 12.96(bs, 2H), 7.88-8.10(m, 3H), 7.70(s, 1H), 7.34(s, 1H), 7.22-7.31(m, 2H), 4.40(s, 1H), 3.57(s, 3H), 1.81(s, 3H), 1.32-1.55(m, 4H), 0.85-0.92(m, 12H).

Example 201
Syntehsis of (E)-3-(4-{4-[3-(cyclohexylpentyloxymethyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methylacrylic acid (B484)

1H-NMR(DMSO-d6) 12.98(bs, 2H), 7.92-8.00(m, 2H), 7.86-7.95(m, 1H), 7.70(s, 1H), 7.34(s, 1H), 7.22-7.30(m, 2H), 4.39(d, 1H, J=7.2 Hz), 3.59(s, 3H), 3.21-3.28(m, 2H), 1.88-2.00(m, 1H), 1.81(s, 3H), 1.44-1.78(m, 6H), 1.00-1.36(m, 10H), 0.83-0.87(m, 3H).

Example 202
Syntehsis of (E)-3-(4-{4-[3-(2,2-dimethylpropyloxy)propyl]-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methylacrylic acid (B488)

1H-NMR(DMSO-d6) 12.97(bs, 2H), 7.92-8.00(m, 2H), 7.84-7.90(m, 1H), 7.73(s, 1H), 7.34(s, 1H), 7.14-7.25(m, 2H), 3.62(s, 3H), 3.45(t, 2H, J=6.3 Hz), 3.06(s, 2H), 2.74(t, 2H, J=6.3 Hz), 1.81-1.90(m, 5H), 1.90(s, 9H).

Example 203
Syntehsis of (E)-3-(2,6-difluoro-4-{4-[3-(3-hexyloxypropyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B505)

1H-NMR(DMSO-d6) 12.97(bs, 2H), 7.92-8.00(m, 2H), 7.86(dd, 1H, J=1.5, 7.5 Hz), 7.72(s, 1H), 7.34(s, 1H), 7.23(dd, 2H, J=1.5, 7.5 Hz), 7.16(t, 1H, J=7.5 Hz), 3.61(s, 3H), 3.20-3.46(m, 4H), 2.69-2.74(m, 2H), 1.76-1.88(m, 5H), 1.46-1.56(m, 2H), 1.20-1.38(m, 6H), 1.84-0.89(m, 3H).

Example 204
Syntehsis of (E)-3-(4-{4-[3-(cyclohexylhexyloxymethyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methylacrylic acid (B519)

1H-NMR(DMSO-d6) 13.00(bs, 2H), 7.92-8.00(m, 2H), 7.89(dd, 1H, J=2.7, 7.5 Hz), 7.70(s, 1H), 7.34(s, 1H), 7.22-7.29(m, 2H), 4.39(d, 1H, J=7.2 Hz), 3.59(s, 3H), 1.90-2.00(m, 1H), 1.81(s, 3H), 1.02-1.76(m, 16H), 1.32-1.55(m, 4H), 0.85(t, 3H, J=6.9 Hz).

Example 205
Syntehsis of (E)-3-[4-(4-{3-[3-(3,3-dimethylbutyloxy)propyl]-2-methyloxyphenyl}thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methylacrylic acid (B521)

1H-NMR(CDCl3-d6) 7.91(s, 1H), 7.88(s, 1H), 7.58(s, 1H), 7.43-7.54(m, 2H), 7.25-7.30(m, 1H), 7.17(t, 1H, J=7.5 Hz), 3.58(s, 3H), 3.46-3.52(m, 4H), 2.80(t, J=8.1 Hz), 1.90-2.30(m, 5H), 1.54(t, 2H, J=7.5 Hz), 0.94(s, 9H).

Example 206
Syntehsis of (Z)-3-(2,6-difluoro-4-{4-[2-fluoro-3-(1-methyloxyhexyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methyloxyacrylic acid (B533)

1H-NMR(DMSO-d6) 12.98 (bs, 2H), 8.00-8.05 (m, 1H), 7.89-7.95 (m, 2H), 7.65 (d, 1H, J=2.4 Hz), 7.31-7.39 (m, 2H), 6.67 (s, 1H), 4.55-4.59 (m, 1H), 3.72 (s, 3H), 3.18 (s, 3H), 1.64-1.76 (m, 2H), 1.26-1.41 (m, 6H), 0.81-0.86 (m, 3H).

Example 207
Syntehsis of (Z)-3-(4-{4-[3-(3-butyloxypropyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methyloxyacrylic acid (B790)

1H-NMR(CDCl3-d6) 7.83(s, 1H), 7.80(s, 1H), 7.48(d, 1H, J=7.8 Hz), 7.44(s, 1H), 7.26-7.30(m, 1H), 7.17(t, 1H, J=7.5 Hz), 6.91(s, 1H), 3.90(s, 3H), 3.58(s, 3H), 3.50(t, 2H, J=6.3 Hz), 3.44(t, 2H, J=6.3 Hz), 2.80(t, 2H, J=8.1 Hz), 1.91-2.05(m, 2H), 1.53-1.63(m, 2H), 1.34-1.46(m, 2H), 0.94(t, 3H, J=7.5 Hz).

Example 208
Syntehsis of (E)-3-(2,6-dichloro-4-{4-[2-fluoro-3-(1-methyloxypropyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B896)

1H-NMR(DMSO-d6) 13.02(bs, 2H), 8.29(s, 2H), 7.95-8.06(m, 1H), 7.65(d, 1H, J=2.4 Hz), 7.32-7.42(m, 3H), 4.52(t, 1H, J=6.3 Hz), 3.20(s, 3H), 1.66-1.84(m, 5H), 0.87(t, 1H, J=7.5 Hz).

Example 209
Syntehsis of (E)-3-(2,6-dichloro-4-{4-[2-fluoro-3-(1-methyloxy-3-propyloxypropyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B897)

Example 210
Syntehsis of (E)-3-(2,6-dichloro-4-{4-[2-fluoro-3-(1-methyloxy-4-pentyloxybutyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B899)

1H-NMR(DMSO-d6) 13.00(bs, 2H), 8.29(s, 2H), 7.97-8.06(m, 1H), 7.64(d, 1H, J=2.4 Hz), 7.31-7.40(m, 3H), 4.60(t, 1H, J=6.0 Hz), 3.19(s, 3H), 1.66-1.82(m, 5), 1.41-1.65(m, 4H), 1.22-1.30(m, 4H), 0.81-0.86(m, 3H).

Example 211
Syntehsis of (E)-3-(2,6-dichloro-4-{4-[2-fluoro-3-(1-methyloxy-3,3-dimethylbutyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B905)

1H-NMR(DMSO-d6) 13.02 (bs, 2H), 8.29 (s, 2H), 7.97-8.03 (m, 1H), 7.65 (d, 1H, J=2.5 Hz), 7.30-7.40 (m, 3H), 4.64-4.68 (m, 1H), 3.25 (s, 3H), 1.69-1.77(m, 4), 1.42-1.48 (m, 1H), 0.97 (s, 9H).

Example 208
Syntehsis of (E)-3-(2,6-dichloro-4-{4-[3-(2,2-dimethyl-1-propyloxypropyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B927)

1H-NMR(DMSO-d6) 13.00 (bs, 2H), 8.30 (s, 2H), 7.99-8.04 (m, 1H), 7.61-7.62 (m, 1H), 7.32-7.41 (m, 3H), 4.40 (s, 1H), 3.16-3.33 (m, 2H), 169 (s, 3H), 1.47-1.55 (m, 2H), 0.84-0.91 (m, 12H).

Example 213
Syntehsis of (E)-3-(2,6-dichloro-4-{4-[3-(cyclohexylpropyloxymethyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B936)

1H-NMR(DMSO-d6) 13.00 (bs, 2H), 8.30 (s, 1H), 7.98-8.03 (m, 1H), 7.63 (d, 1H, J=2.3 Hz), 7.32-7.40 (m, 3H), 4.40 (d, 1H, J=7.0 Hz), 3.18-3.23 (m, 2H), 1.93-1.97 (m, 1H), 1.04-1.64 (m, 12H), 0.86 (t, 3H, J=7.5 Hz).

Example 214
Syntehsis of (E)-3-(4-{4-[3-(1-butyloxy-2,2-dimethylpropyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}-2,6-dichlorophenyl)-2-methylacrylic acid (B958)

1H-NMR(DMSO-d6) 13.00 (bs, 2H), 8.29 (s, 2H), 7.99-8.04 (m, 1H), 7.61-7.62 (m, 1H), 7.32-7.41 (m, 3H), 4.40 (s, 1H), 3.32 (t, 2H, J=6.3 Hz), 169 (s, 3H), 1.29-1.53 (m, 4H), 0.84-0.91 (m, 12H).

Example 215
Syntehsis of (E)-3-(4-{4-[3-(butyloxycyclohexylmethyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}-2,6-dichlorophenyl)-2-methylacrylic acid (B967)

1H-NMR(DMSO-d6) 13.00 (bs, 2H), 8.29 (s, 1H), 7.98-8.03 (m, 1H), 7.63 (d, 1H, J=2.3 Hz), 7.32-7.40 (m, 3H), 4.40 (d, 1H, J=7.0 Hz), 3.18-3.23 (m, 2H), 1.93-1.97 (m, 1H), 1.04-1.64 (m, 14H), 0.86 (t, 3H, J=7.5 Hz).

Example 216
Syntehsis of (E)-3-(2,6-dichloro-4-{4-[2-methyloxy-3-(1-methyloxy-5-methylhexyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1053)

1H-NMR(DMSO-d6) 12.98 (bs, 2H), 9.29 (s, 1H), 7.89-7.92 (m, 1H), 7.72 (s, 1H), 7.41 (s, 1H), 7.24-7.37 (m, 3H), 4.53-4.57 (m, 1H), 3.61 (s, 3H), 3.16 (s, 3H), 0.87-1.72 (m, 16H).

Example 217
Syntehsis of (E)-3-(2,6-dichloro-4-{4-[2-methyloxy-3-(1-methyloxy-3,3-dimethylbutyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1054)

1H-NMR(DMSO-d6) 12.99(bs, 2H), 8.29(s, 2H), 7.89(dd, 1H, J=1.6, 7.5 Hz), 7.71(s, 1H), 7.40(d, 1H, J=1.5 Hz), 7.34(dd, 1H, J=2.1, 7.8 Hz), 7.25(t, 1H, J=7.8 Hz), 4.69(d, 1H, J=7.5 Hz), 3.63(s, 3H), 3.13(s, 3H), 1.63-1.71(m, 4H), 1.36-1.44(m, 1H), 1.00(s, 9H).

Example 218
Syntehsis of (E)-3-(2,6-dichloro-4-{4-[2-methyloxy-3-(1-methyloxydecyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1059)

1H-NMR(DMSO-d6) 13.00(bs, 2H), 8.29(s, 2H), 7.92(dd, 1H, J=2.4, 7.2 Hz), 7.72(s, 1H), 7.41(d, 1H, J=1.2 Hz), 7.24-7.38(m, 2H), 4.55-4.59(m, 1H), 3.62(s, 3H), 3.15(s, 3H), 1.50-1.78(m, 4H), 1.18-1.50(m, 15H), 0.82-0.87(m, 3H).

Example 219
Syntehsis of (E)-3-(2,6-dichloro-4-{4-[2-methyloxy-3-(1-methyloxy-undecyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1060)

1H-NMR(DMSO-d6) 13.00(bs, 2H), 8.29(s, 2H), 7.92(dd, 1H, J=2.4, 7.5 Hz), 7.72(s, 1H), 7.41(d, 1H, J=1.5 Hz), 7.24-7.33(m, 2H), 4.55-4.59(m, 1H), 3.62(s, 3H), 3.16(s, 3H), 1.50-1.78(m, 4H), 1.18-1.50(m, 17H), 0.82-0.87(m, 3H).

Example 220
Syntehsis of (E)-3-(2,6-dichloro-4-{4-[3-(cyclohexylpropyloxymethyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1102)

1H-NMR(DMSO-d6) 12.99(bs, 2H), 8.29(s, 2H), 7.89(dd, 1H, J=2.1, 7.5 Hz), 7.70(s, 1H), 7.41(d, 1H, J=1.5 Hz), 7.30(dd, 1H, J=2.1, 7.5 Hz), 7.25(t, 1H, J=7.5 Hz), 4.40(d, 1H, J=6.9 Hz), 3.59(s, 3H), 3.17-3.24(m, 2H), 1.88-2.00(m, 1H), 1.69(s, 3H), 1.44-1.70(m, 4H), 1.00-1.38(m, 6H), 0.87(t, 3H, J=7.2 Hz).

Example 221
Syntehsis of (E)-3-(4-{4-[3-(1-butyloxyethyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}-2,6-dichlorophenyl)-2-methylacrylic acid (B1122)

1H-NMR(DMSO-d6) 12.99(bs, 2H), 8.29(s, 2H), 7.91(dd, 1H, J=1.8, 7.8 Hz), 7.72(s, 1H), 7.40(d, 1H, J=1.2 Hz), 7.37(dd, 1H, J=1.5, 7.5 Hz), 7.27(t, 1H, J=7.8 Hz), 4.80-4.86(m, 1H), 3.62(s, 3H), 1.69(s, 3H), 1.23-1.55(m, 7H), 0.85(t, 3H, J=7.2 Hz).

Example 222
Syntehsis of (E)-3-(4-{4-[3-(3-butyloxypropyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}-2,6-dichlorophenyl)-2-methylacrylic acid (B1124)

1H-NMR(CDCl3-d6) 8.32(s, 2H), 7.65(s, 1H), 7.49(d, 1H, J=9.0 Hz), 7.46(s, 1H), 7.24-7.28(m, 1H), 7.17(t, 1H, J=7.5 Hz), 3.58(s, 3H), 3.49(t, 2H, J=6.6 Hz), 3.44(t, 2H, J=6.6 Hz), 2.79(t, 2H, J=7.8 Hz), 1.90-2.05(m, 2H), 1.86(bs, 3H), 1.53-1.63(m, 2H), 1.33-1.46(m, 2H), 0.93(t, 3H, J=7.5 Hz).

Example 223
Syntehsis of (E)-3-(2,6-dichloro-4-{4-[2-fluoro-3-(1-methyloxyhexyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methyloxyacrylic acid (B1238)

1H-NMR(DMSO-d6) 13.01 (bs, 2H), 8.25 (s, 2H), 7.99-8.05 (m, 1H), 7.65 (d, 1H, J=2.6 Hz), 7.31-7.39 (m, 2H), 6.73 (s, 1H), 4.55-4.59 (m, 1H), 3.62 (s, 3H), 3.18 (s, 3H), 1.61-1.79 (m, 2H), 1.26-1.41 (m, 6H), 0.80-0.86 (m, 3H).

Example 224
Syntehsis of (Z)-3-(2,6-dichloro-4-{4-[2-fluoro-3-(1-methyloxydecyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methyloxyacrylic acid (B1250)

1H-NMR(DMSO-d6) 12.97(bs, 1H), 8.25(s, 2H), 8.05(t, 1H, J=7.6 Hz), 7.64(s, 1H), 7.33-7.35(m, 2H), 6.73(s, 1H), 4.56(t, 1H, J=7.6 Hz), 3.61(s, 3H), 3.17(s, 3H), 1.70-1.80(m, 2H), 1.22-1.38(m, 14H), 0.87-0.90(m, 3H).

Example 225
Syntehsis of (Z)-3-(2,6-dichloro-4-{4-[2-methyloxy-3-(1-methyloxydecyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methyloxyacrylic acid (B1437)

1H-NMR(DMSO-d6) 12.99(bs, 1H), 8.25(s, 2H), 7.89-7.94(m, 1H), 7.72(s, 1H), 7.24-7.34(m, 2H), 6.73(s, 1H), 4.55-4.59(m, 1H), 3.62(s, 6H), 3.15(s, 3H), 1.18-1.80(m, 16H), 0.82-0.87(m, 3H).

Example 226
Syntehsis of (Z)-3-(2,6-dichloro-4-{4-[2-methyloxy-3-(1-methyloxyundecyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methyloxyacrylic acid (B1438)

1H-NMR(DMSO-d6) 12.99(bs, 1H), 8.25(s, 2H), 7.89-7.94(m, 1H), 7.72(s, 1H), 7.24-7.34(m, 2H), 6.73(s, 1H), 4.55-4.59(m, 1H), 3.62(s, 6H), 3.15(s, 3H), 1.18-1.80(m, 18H), 0.82-0.87(m, 3H).

Example 227
Syntehsis of (E)-3-(4-{4-[3-(2-ethyloxy-1-methyloxypropyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methylacrylic acid (B1728)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 8.06(t, 1H, J=7.5 Hz), 7.96(s, 1H), 7.93(s, 1H), 7.66(s, 1H), 7.30-7.40(m, 3H), 4.72(t, 1H, J=6.5 Hz), 3.55-3.68(m, 2H), 3.47(q, 2H, J=7.0 Hz), 3.25(s, 3H), 1.79(s, 3H), 1.10(t, 3H, J=7.0 Hz).

Example 228
Syntehsis of (Z)-3-(4-{4-[3-(2-ethyloxy-1-methyloxypropyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methyloxyacrylic acid (B1729)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 8.06(t, 1H, J=7.5 Hz), 7.92(s, 1H), 7.90(s, 1H), 7.66(s, 1H), 7.30-7.40(m, 2H), 6.65(s, 1H), 4.72(t, 1H, J=6.5 Hz), 3.71(s, 3H), 3.55-3.68(m, 2H), 3.47(q, 2H, J=7.0 Hz), 3.25(s, 3H), 1.10(t, 3H, J=7.0 Hz).

Example 229
Syntehsis of (E)-3-(4-{4-[3-(2-butyloxy-1-methyloxyethyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methylacrylic acid (B1730)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 8.06(t, 1H, J=7.5 Hz), 7.96(s, 1H), 7.93(s, 1H), 7.66(s, 1H), 7.30-7.40(m, 3H), 4.72(t, 1H, J=6.5 Hz), 3.55-3.68(m, 2H), 3.42(t, 2H, J=7.0 Hz), 3.25(s, 3H), 1.79(s, 3H), 1.40-1.50(m, 2H), 1.22-1.34(m, 2H), 0.80(t, 3H, J=7.0 Hz).

Example 230
Syntehsis of (Z)-3-(4-{4-[3-(2-butyloxy-1-methyloxyethyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methyloxyacrylic acid (B1731)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 8.06(t, 1H, J=7.5 Hz), 7.92(s, 1H), 7.90(s, 1H), 7.66(s, 1H), 7.30-7.40(m, 2H), 6.65(s, 1H), 4.72(t, 1H, J=6.5 Hz), 3.71(s, 3H), 3.55-3.68(m, 2H), 3.42(t, 2H, J=7.0 Hz), 3.25(s, 3H), 1.40-1.50(m, 2H), 1.22-1.34(m, 2H), 0.80(t, 3H, J=7.0 Hz).

Example 231
Syntehsis of (E)-3-[2,6-difluoro-4-(4-{2-fluoro-3-[1-methyloxy-2-(3-methylbutyloxy)ethyl]phenyl}thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1732)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 8.06(t, 1H, J=7.5 Hz), 7.96(s, 1H), 7.93(s, 1H), 7.66(s, 1H), 7.30-7.40(m, 3H), 4.72(t, 1H, J=6.5 Hz), 3.55-3.68(m, 2H), 3.42(t, 2H, J=7.0 Hz), 3.25(s, 3H), 1.79(s, 3H), 1.50-1.60(m, 1H), 1.22-1.34(m, 2H), 0.85(d, 6H, J=6.0 Hz).

Example 232
Syntehsis of (Z)-3-[2,6-difluoro-4-(4-{2-fluoro-3-[1-methyloxy-2-(3-methylbutyloxy)ethyl]phenyl}thiazol-2-ylcarbamoyl}phenyl)-2-methyloxyacrylic acid (B1733)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 8.06(t, 1H, J=7.5 Hz), 7.92(s, 1H), 7.90(s, 1H), 7.66(s, 1H), 7.30-7.40(m, 2H), 6.65(s, 1H), 4.72(t, 1H, J=6.5 Hz), 3.68(s, 3H), 3.55-3.68(m, 2H), 3.42(t, 2H, J=7.0 Hz), 3.25(s, 3H), 1.50-1.60(m, 1H), 1.22-1.34(m, 2H), 0.85(d, 6H, J=6.0 Hz).

Example 233
Syntehsis of (E)-3-(2,6-difluoro-4-{4-[3-(2-ethyloxy-1-methyloxyethyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1734)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 8.29(s, 2H), 8.06(t, 1H, J=7.5 Hz), 7.64(s, 1H), 7.30-7.40(m, 3H), 4.72(t, 1H, J=6.5 Hz), 3.55-3.68(m, 2H), 3.47(q, 2H, J=7.0 Hz), 3.25(s, 3H), 1.69(s, 3H), 1.10(t, 3H, J=7.0 Hz).

Example 234
Syntehsis of (Z)-3-(2,6-dichloro-4-{4-[3-(2-ethyloxy-1-methyloxyethyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methyloxyacrylic acid (B1735)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 8.29(s, 2H), 8.06(t, 1H, J=7.5 Hz), 7.64(s, 1H), 7.30-7.40(m, 2H), 6.65(s, 1H), 4.72(t, 1H, J=6.5 Hz), 3.71(s, 3H), 3.55-3.68(m, 2H), 3.47(q, 2H, J=7.0 Hz), 3.25(s, 3H), 1.10(t, 3H, J=7.0 Hz).

Example 235
Syntehsis of (E)-3-(4-{4-[3-(2-butyloxy-1-methyloxyethyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}-2,6-dichlorophenyl)-2-methylacrylic acid (B1736)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 8.29(s, 2H), 8.06(t, 1H, J=7.5 Hz), 7.64(s, 1H), 7.30-7.40(m, 3H), 4.72(t, 1H, J=6.5 Hz), 3.55-3.68(m, 2H), 3.42(t, 2H, J=7.0 Hz), 3.25(s, 3H), 1.69(s, 3H), 1.40-1.50(m, 2H), 1.22-1.34(m, 2H), 0.80(t, 3H, J=7.0 Hz).

Example 236
Syntehsis of (Z)-3-(4-{4-[3-(2-butyloxy-1-methyloxyethyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}-2,6-dichlorophenyl)-2-methyloxyacrylic acid (B1737)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 8.29(s, 2H), 8.06(t, 1H, J=7.5 Hz), 7.64(s, 1H), 7.30-7.40(m, 2H), 6.65(s, 1H), 4.72(t, 1H, J=6.5 Hz), 3.55-3.68(m, 2H), 3.61(s, 3H), 3.42(t, 2H, J=7.0 H), 3.25(s, 3H), 1.40-1.50(m, 2H), 1.22-1.34(m, 2H), 0.80(t, 3H, J=7.0 Hz).

Example 237
Syntehsis of (E)-3-[2,6-dichloro-4-(4-{2-fluoro-3-[1-methyloxy-2-(3-methylbutyloxy)ethyl]phenyl}thiazol-2-ylcarbamoyl)phenyl]-2-methylacrylic acid (B1738)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 8.29(s, 2H), 8.06(t, 1H, J=7.5 Hz), 7.64(s, 1H), 7.30-7.40(m, 3H), 4.72(t, 1H, J=6.5 Hz), 3.55-3.68(m, 2H), 3.42(t, 2H, J=7.0 Hz), 3.25(s, 3H), 1.79(s, 3H), 1.50-1.60(m, 1H), 1.22-1.34(m, 2H), 0.85(d, 6H, J=6.0 Hz).

Example 238
Syntehsis of (Z)-3-[2,6-dichloro-4-(4-{2-fluoro-3-[1-methyloxy-2-(3-methylbutyloxy)ethyl]phenyl}thiazol-2-ylcarbamoyl)phenyl]-2-methyloxyacrylic acid (B1739)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 8.29(s, 2H), 8.06(t, 1H, J=7.5 Hz), 7.64(s, 1H), 7.30-7.40(m, 2H), 6.65(s, 1H), 4.72(t, 1H, J=6.5 Hz), 3.55-3.68(m, 2H), 3.61(s, 3H), 3.42(t, 2H, J=7.0 Hz), 3.25(s, 3H), 1.50-1.60(m, 1H), 1.22-1.34(m, 2H), 0.85(d, 6H, J=6.0 Hz).

Example 239
Syntehsis of (E)-3-{2,6-difluoro-4-[6-(3-methyloxy-3-methylbutyl)-4,5-dihydronaphthino[1,2-d]thiazol-2-ylcarbamoyl]phenyl}-2-methylacrylic acid (B1742)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 7.99(s, 1H), 7.96(s, 1H), 7.93(t, 1H, J=7.5 Hz), 7.62(d, 1H, J=2.3 Hz), 7.33(s, 1H), 7.19-7.28(m, 2H), 3.62(t, 2H, J=6.7 Hz), 2.69(t, 2H, J=6.7 Hz), 1.79(s, 3H), 1.70-1.79(m, 2H), 1.58-1.69(m, 2H), 1.30-1.49(m, 2H).

Example 240
Syntehsis of (E)-3-(2,6-difluoro-4-{4-[2-fluoro-3-(1-methyloxy-3-methylsufanylpropyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1744)

1H-NMR(DMSO-d6) 13.02(bs, 2H), 7.92-8.08(m, 3H), 7.67(d, 1H, J=2.7 Hz), 7.30-7.44(m, 3H), 4.71-4.75(m, 1H), 3.20(s, 3H), 2.56(t, 2H, J=7.5 Hz), 1.76-2.10(m, 8H).

Example 241
Syntehsis of (E)-3-(4-{4-[3-(3-t-butyloxybutyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl]-2-methylacrylic acid (B1746)

1H-NMR(DMSO-d6) 13.00(bs, 2H), 7.90-8.00(m, 3H), 7.64(d, 1H, J=2.7 Hz), 7.20-7.34(m, 3H), 3.66-3.71(m, 1H), 2.64-2.77(m, 2H), 1.81(s, 3H), 1.62-1.70(m, 2H), 1.07-1.15(m, 12H).

Example 242
Syntehsis of (E)-3-(2,6-difluoro-4-{4-[2-fluoro-3-(3-methyloxyheptyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1747)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 7.96(s, 1H), 7.93(s, 1H), 7.93(t, 1H, J=7.5 Hz), 7.64(s, 3H), 7.33(s, 1H), 7.20-7.30(m, 2H), 3.25(s, 3H), 3.17-3.22(m, 1H), 2.65-2.72(m, 2H), 1.78(s, 3H), 1.70-1.78(m, 2H), 1.45-1.53(m, 2H), 1.22-1.38(m, 4H), 0.87-0.90(m, 3H).

Example 243
Syntehsis of (E)-3-[2,6-difluoro-4-(4-{2-fluoro-3-[3-(2-methyloxyethyloxy)propyl]phenyl}thiazol-2-ylcarbamoyl)phenyl]-2-methylacrylic acid (B1748)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 7.96(s, 1H), 7.93(s, 1H), 7.93(t, 1H, J=7.5 Hz), 7.64(s, 1H), 7.33(s, 1H), 7.20-7.30(m, 2H), 3.40-3.50(m, 6H), 3.25(s, 3H), 2.74(t, 2H, J=7.4 Hz), 1.80-1.88(m, 2H), 1.80(s, 3H).

Example 244
Syntehsis of (E)-3-{4-[4-(3-{1-[2-(2-ethyloxyethyloxy)ethyloxy]propyl}-2-fluorophenyl)thiazol-2-ylcarbamoyl]-2,6-difluorophenyl}-2-methylacrylic acid (B1749)

1H-NMR(DMSO-d6) 13.00(bs, 2H), 7.92-8.07(m, 3H), 7.65(d, 1H, J=2.4 Hz), 7.31-7.44(m, 3H), 4.67(t, 1H, J=6.3 Hz), 3.20-3.56(m, 10H), 1.67-1.82(m, 5H), 1.09(t, 3H, J=7.2 Hz), 0.89(t, 3H, J=7.2 Hz).

Example 245
Syntehsis of (E)-3-[2,6-difluoro-4-(4-{2-fluoro-3-[3-(teterahydrofuran-2-ylmethyloxy)propyl]phenyl}thiazol-2-ylcarbamoyl)phenyl]-2-methylacrylic acid (B1750)

1H-NMR(DMSO-d6) 13.01(bs, 2H), 7.90-7.95(m, 3H), 7.64(d, 1H, J=2.4 Hz), 7.20-7.36(m, 3H), 3.89-3.97(m, 1H), 3.69-3.76(m, 1H), 3.58-3.65(m, 1H), 3.45(t, 4H, J=6.3 Hz), 2.74(t, 2H, J=7.5 Hz), 1.70-1.94(m, 8H), 1.50-1.60(m, 1H).

Example 246
Syntehsis of (E)-3-(2,6-dichloro-4-{4-[2-fluoro-3-(3-methyloxyheptyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1751)

1H-NMR(DMSO-d6) 12.97(bs, 1H), 8.29(s, 2H), 7.85(t, 1H, J=7.6 Hz), 7.64(s, 1H), 7.40(s, 1H), 7.20-7.31(m, 2H), 3.25(s, 3H), 3.17-3.22(m, 1H), 2.65-2.72(m, 2H), 1.70-1.80 (m, 2H), 1.68(s, 3H), 1.45-1.53(m, 2H), 1.22-1.38(m, 4H), 0.87-0.90(m, 3H).

Example 247
Syntehsis of (E)-3-(2,6-dichloro-4-{4-[2-fluoro-3-(3-methyloxydecyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1752)

1H-NMR(DMSO-d6) 12.97(bs, 1H), 8.28(s, 2H), 7.94(t, 1H, J=7.6 Hz), 7.64(s, 1H), 7.40 (s, 1H), 7.20-7.31(m, 2H), 3.20(s, 3H), 3.17-3.22(m, 1H), 2.65-2.72(m, 2H), 1.70-1.80(m, 2H), 1.68(s, 3H), 1.45-1.53(m, 2H), 1.22-1.38(m, 8H), 0.87-0.90(m, 3H).

Example 248
Syntehsis of (E)-3-[2,6-dichloro-4-(4-{2-fluoro-3-[3-(2-methyloxyethyloxy)propyl]phenyl}thiazol-2-ylcarbamoyl)phenyl]-2-methylacrylic acid (B1753)

1H-NMR(DMSO-d6) 12.97(bs, 1H), 8.28(s, 2H), 7.94(t, 1H, J=7.6 Hz), 7.64(s, 1H), 7.40(s, 1H), 7.20-7.31(m, 2H), 3.40-3.50(m, 6H), 3.25(s, 3H), 2.73(t, 2H, J=7.4 Hz), 1.80-1.88(m, 2H), 1.68(s, 3H).

Example 249
Syntehsis of (E)-3-{2,6-dichloro-4-[4-(3-{1-[2-(2-ethyloxyethyloxy)ethyloxy]propyl]-2-fluorophenyl}thiazol-2-ylcarbamoyl)phenyl]-2-methylacrylic acid (B1754)

1H-NMR(DMSO-d6) 13.01(bs, 2H), 8.29(s, 2H), 8.02(dt, 1H, J=1.8, 7.5 Hz), 7.64(d, 1H, J=2.4 Hz), 7.38-7.44(m, 2H), 7.33(t, 1H, J=7.5 Hz), 4.67(t, 1H, J=6.0 Hz), 3.39-3.56(m, 10H), 1.67-1.78(m, 5H), 1.09(t, 3H, J=7.2 Hz), 0.89(t, 3H, J=6.9 Hz),

Example 250
Syntehsis of (E)-3-[2,6-dichloro-4-(4-{2-fluoro-3-[3-(tetrahydrofuran-2-ylmethyloxy)propyl]phenyl}thiazol-2-ylcarbamoyl)phenyl]-2-methylacrylic acid (B1755)

1H-NMR(DMSO-d6) 13.02(bs, 2H), 8.29(s, 2H), 7.94(dt, 1H, J=2.1, 7.2 Hz), 7.64(d, 1H, J=2.7 Hz), 7.40(d, 1H, J=1.2 Hz), 7.20-7-32(m, 2H), 3.89-3.97(m, 1H), 3.69-3.76(m, 1H), 3.58-3.65(m, 1H), 3.45(t, 2H, J=6.6 Hz), 2.74(t, 2H, J=7.2 Hz), 1.73-1.94(m, 4H), 1.69(d, 3H, J=1.8 Hz), 1.50-1.59(m, 1H)

Example 251
Syntehsis of (E)-3-(4-{4-[3-(3-ethyloxypropyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl]-2,6-difluorophenyl}-2-methylacrylic acid (B1756)

1H-NMR(DMSO-d6) 13.01(bs, 2H), 7.90-8.10(m, 3H), 7.64(d, 1H, J=2.4 Hz), 7.20-7.38(m, 3H), 3.20-3.45(m, 4H), 2.73(t, 2H, J=7.8 Hz), 1.76-1.88(m, 5H), 1.12(d, 3H, J=6.9 Hz).

Example 252
Syntehsis of (E)-3-(2,6-dichloro-4-{4-[3-(3-ethyloxypropyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1757)

1H-NMR(DMSO-d6) 13.02(bs, 2H), 8.29(s, 2H), 7.94(dt, 1H, J=1.8, 6.9 Hz), 7.64(d, 1H, J=2.7 Hz), 7.20-7.33(m, 3H), 3.30-3.45(m, 2H), 2.70-2.78(m, 2H), 1.78-1.85(m, 2H), 1.69(d, 3H, J=1.5 Hz), 1.12(t, 3H, J=7.2 Hz).

Example 253
Syntehsis of (E)-3-[2,6-dichloro-4-(4-{3-[2-(2-ethyloxyethyloxy)ethyloxymethyl]-2-fluorophenyl}thiazol-2-ylcarbamoyl)phenyl]-2-methylacrylic acid (B1762)

1H-NMR(DMSO-d6) 13.02(bs, 2H), 8.29(s, 2H), 8.05(dt, 1H, J=1.8, 7.8 Hz), 7.40-7.48(m, 2H), 7.32(d, 1H, J=7.8 Hz), 4.64(s, 2H), 3.56-3.66(m, 4H), 3.50-3.55(m, 2H), 3.39-3.48(m, 4H), 1.09(d, 3H, J=7.2 Hz).

Example 254
Syntehsis of (E)-3-{4-[4-(3-ethyloxymethyl-2-fluorophenyl)thiazol-2-ylcarbamoyl]-2,6-difluorophenyl]-2-methylacrylic acid (B1763)

1H-NMR(DMSO-d6) 13.02(bs, 2H), 7.92-8.00(m, 3H), 7.66(d, 1H, J=2.7 Hz), 7.40-7.47(m, 1H), 7.28-7.37(m, 3H), 4.59(s, 2H), 3.52-3.59(m, 2H), 1.81(d, 3H, J=1.8 Hz), 1.14-1.20(m, 3H).

Example 255
Syntehsis of (E)-3-{2,6-dichloro-4-[4-(3-ethyloxymethyl-2-fluorophenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methylacrylic acid (B1764)

1H-NMR(DMSO-d6) 13.02(bs, 2H), 8.29(d, 2H, J=1.2 Hz), 8.00-8.10(m, 1H), 7.66(d, 1H, J=2.4 Hz), 7.38-7.47(m, 2H), 7.31(t, 1H, J=7.5 Hz), 4.59(s, 2H), 3.52-3.59(m, 2H), 1.69(d, 3H, J=0.9 Hz), 1.14-1.20(m, 3H).

Example 256
Syntehsis of (E)-3-{2,6-difluoro-4-[4-(2-fluoro-3-propyloxymethylphenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methylacrylic acid (B1765)

1H-NMR(DMSO-d6) 13.02(bs, 2H), 7.92-8.08(m, 3H), 7.66(d, 1H, J=2.4 Hz), 7.40-7.47(m, 1H), 7.28-7.38(m, 3H), 4.59(s, 2H), 3.46(t, 2H, J=6.6 Hz), 1.81(s, 3H), 1.51-1.64 (m, 2H), 0.90(t, 3H, J=7.5 Hz).

Example 257
Syntehsis of (E)-3-{2,6-dichloro-4-[4-(2-fluoro-3-propyloxymethylphenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methylacrylic acid (B1766)

1H-NMR(DMSO-d6) 13.01(bs, 2H), 8.29(s, 2H), 8.04(dt, 1H, J=2.1, 7.8 Hz), 7.65(d, 1H, J=2.4 Hz), 7.38-7.47(m, 2H), 7.31(t, 1H, J=6.6 Hz), 4.59(s, 2H), 3.46(t, 2H, J=6.6 Hz), 1.69(d, 3H, J=1.2 Hz), 1.52-1.63 (m, 4H), 0.90(t, 3H, J=7.5 Hz).

Example 258
Syntehsis of (E)-3-(4-{4-[3-(4-ethyloxybutyloxymethyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}-2,6-dfluorophenyl}-2-methylacrylic acid (B1767)

1H-NMR(DMSO-d6) 13.02(bs, 2H), 7.92-8.08(m, 3H), 7.66(d, 1H, J=2.7 Hz), 7.40-7.46(m, 1H), 7.28-7.36(m, 3H), 4.59(s, 2H), 3.51(t, 2H, J=6.0 Hz), 3.25-3.42(m, 4H), 1.69(d, 3H, J=1.2 Hz), 1.81(d, 3H, J=1.8 Hz), 1.50-1.65 (m, 4H), 1.09(t, 3H, J=6.9 Hz).

Example 259
Syntehsis of (E)-3-(2,6-dichloro-4-{4-[3-(4-ethyloxybutyloxymethyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}phenyl}-2-methylacrylic acid (B1768)

1H-NMR(DMSO-d6) 13.02(bs, 2H), 8.29(s, 2H), 8.05(dt, 1H, J=1.8, 8.1 Hz), 7.66(d, 1H, J=2.4 Hz), 7.39-7.46(m, 2H), 7.32(t, 1H, J=7.8 Hz), 4.59(s, 2H), 3.50(t, 2H, J=6.3 Hz), 3.25-3.41(m, 4H), 1.69(d, 3H, J=1.2 Hz), 1.50-1.62 (m, 4H), 1.08(t, 3H, J=6.9 Hz).

Example 260
Syntehsis of (E)-3-(2,6-difluoro-4-{4-[2-fluoro-3-(3-methylbutyloxymethyl)phenyl]thiazol-2-ylcarbamoyl}phenyl}-2-methylacrylic acid (B1769)

1H-NMR(DMSO-d6) 13.02(bs, 2H), 7.92-8.08(m, 3H), 7.66(d, 1H, J=2.4 Hz), 7.39-7.46(m, 1H), 7.29-7.36(m, 3H), 4.86(s, 2H), 3.52(t, 2H, J=6.9 Hz), 1.63-1.81(d, 3H, J=1.8 Hz), 1.65-1.75(m, 1H), 1.42-1.49 (m, 2H), 0.87(d, 6H, J=6.3 Hz).

Example 261
Syntehsis of (E)-3-(2,6-dichloro-4-{4-[2-fluoro-3-(3-methylbutyloxymethyl)phenyl]thiazol-2-ylcarbamoyl}phenyl}-2-methylacrylic acid (B1770)

1H-NMR(DMSO-d6) 13.02(bs, 2H), 8.29(s, 2H), 8.01-8.08(m, 1H), 7.65(d, 1H, J=2.7 Hz), 7.39-7.46(m, 2H), 7.31(t, 1H, J=7.8 Hz), 4.59(s, 2H), 3.52(t, 2H, J=6.9 Hz), 1.63-1.76(m, 4H), 1.42-1.49 (m, 2H), 0.87(d, 6H, J=6.6 Hz).

Example 262
Syntehsis of (E)-3-(4-{4-[3-(1,4-dimethyloxybutyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}-2,6-difluophenyl}-2-methylacrylic acid (B1771)

1H-NMR(DMSO-d6) 13.01(bs, 2H), 7.92-8.08(m, 3H), 7.66(d, 1H, J=2.7 Hz), 7.29-7.40(m, 3H), 4.55-4.62(m, 1H), 3.19(s, 6H), 1.48-1.90(m, 7H).

Example 263
Syntehsis of (E)-3-(2,6-dichloro-4-{4-[3-(1,4-dimethyloxybutyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}phenyl}-2-methylacrylic acid (B1772)

1H-NMR(DMSO-d6) 13.02(bs, 2H), 8.29(s, 2H), 7.97-8.06(m, 1H), 7.65(d, 1H, J=2.7 Hz), 7.32-7.42(m, 3H), 4.50-4.62(m, 1H), 3.19(s, 6H), 1.40-1.85(m, 7H).

Example 264
Syntehsis of (Z)-3-[2,6-dichloro-4-(4-{3-[3-(2-ethyloxybutyloxy)propyl]-2-fluorophenyl}thiazol-2-ylcarbamoyl}phenyl}-2-methyloxyacrylic acid (B1773)

1H-NMR(DMSO-d6) 12.97(bs, 1H), 8.28(s, 2H), 7.95(t, 1H, J=7.6 Hz), 7.61(s, 1H), 7.25-7.35(m, 2H), 6.73(s, 1H), 3.61(s, 3H), 3.39(s, 3H), 3.25(t, 2H, J=6.0 Hz), 2.74(t, 2H, J=7.4 Hz), 1.80-1.90(m, 2H), 1.22-1.38(m, 5H), 0.87(t, 6H, J=7.4 Hz).

Example 265
Syntehsis of (E)-3-[2,6-difluoro-4-(4-{2-fluoro-3-[3-(2,2,2-trifluoroethyloxy)propyl]phenyl}thiazol-2-ylcarbamoyl}phenyl}-2-methylacrylic acid (B1774)

1H-NMR(DMSO-d6) 13.02(bs, 2H), 7.91-8.00(m, 3H), 7.64(d, 1H, J=2.4 Hz), 7.22-7.35(m, 3H), 4.01-4.11(m, 2H), 3.64(t, 2H, J=6.0 Hz), 2.75(t, 2H, J=7.5 Hz), 1.84-1.93(m, 2H), 1.69(d, 3H, J=1.5 Hz).

Example 266
Syntehsis of (E)-3-[2,6-dichloro-4-(4-{2-fluoro-3-[3-(2,2,2-trifluoroethyloxy)propyl]phenyl}thiazol-2-ylcarbamoyl}phenyl}-2-methylacrylic acid (B1775)

1H-NMR(DMSO-d6) 13.02(bs, 2H), 8.29(s, 2H), 7.95(dt, 1H, J=2.1, 7.2 Hz), 7.64(d, 1H, J=2.4 Hz), 7.41(d, 1H, J=1.5 Hz), 7.22-7.33(m, 2H), 4.01-4.11(m, 2H), 3.64(t, 2H, J=6.3 Hz), 2.75(t, 2H, J=7.5 Hz), 1.84-1.93(m, 2H), 1.81(d, 3H, J=1.5 Hz).

Example 267
Syntehsis of (E)-3-[2,6-difluoro-4-(4-{2-fluoro-3-[3-(3-methyloxybutyloxy)propyl]phenyl}thiazol-2-ylcarbamoyl}phenyl}-2-methylacrylic acid (B1776)

1H-NMR(DMSO-d6) 13.01(bs, 2H), 7.91-8.02(m, 3H), 7.67(d, 1H, J=2.7 Hz), 7.20-7.37(m, 3H), 3.24-3.45(m, 5H), 3.20(s, 3H), 2.70-2.78(m, 2H), 1.77-1.88(m, 5H), 1.55-1.75(m, 2H), 1.08(d, 3H, J=6.3 Hz).

Example 268
Syntehsis of (E)-3-[2,6-dichloro-4-(4-{2-fluoro-3-[3-(3-methyloxybutyloxy)propyl]phenyl}thiazol-2-ylcarbamoyl}phenyl}-2-methylacrylic acid (B1777)

1H-NMR(DMSO-d6) 13.01(bs, 2H), 8.29(s, 2H), 7.90-8.08(m, 1H), 7.63(d, 1H, J=2.7 Hz), 7.41(s, 1H), 7.21-7.32(m, 2H), 3.36-3.45(m, 5H), 3.20(s, 3H), 2.71-2.77(m, 2H), 1.78-1.88(m, 2H), 1.55-1.75(m, 5H), 1.08(d, 3H, J=6.3 Hz).

Example 269
Syntehsis of (Z)-3-[2,6-dichloro-4-(4-{2-fluoro-3-[3-(3-methyloxybutyloxy)propyl]phenyl}thiazol-2-ylcarbamoyl}phenyl}-2-methyloxyacrylic acid (B1778)

1H-NMR(DMSO-d6) 12.99(bs, 1H), 8.25(s, 2H), 7.94(dt, 1H, J=1.5, 6.6 Hz), 7.62(d, 1H, J=2.7 Hz), 7.21-7.32(m, 2H), 6.73(s, 1H), 3.61(s, 3H), 3.37-3.44(m, 5H), 3.20(s, 3H), 1.76-1.84(m, 2H), 1.52-1.75(m, 2H), 1.08(d, 3H, J=6.0 Hz).

Example 270
Syntehsis of (E)-3-(4-{4-[3-(ethyloxyphenylmethyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl}-2-methylacrylic acid (B1779)

1H-NMR(DMSO-d6) 13.00 (bs, 2H), 7.93-8.02 (m, 3H), 7.62 (d, 1H, J=2.6 Hz), 7.49-7.53 (m, 1H), 7.25-7.41(m, 7H), 5.78 (s, 1H), 3.51 (q, 2H, J=7.0 Hz), 1.83 (s, 3H), 1.20 (t, 3H, J=7.0 Hz).

Example 271
Syntehsis of (E)-3-(2,6-dichloro-4-{4-[3-(ethyloxypehnylmethyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1780)

1H-NMR(DMSO-d6) 13.00 (bs, 2H), 8.30 (s, 2H), 7.98-8.02 (m, 1H), 7.61 (d, 1H, J=2.6 Hz), 7.49-7.53 (m, 1H), 7.25-7.41(m, 7H), 5.78 (s, 1H), 3.51 (q, 2H, J=7.0 Hz), 1.66 (s, 3H), 1.20 (t, 3H, J=7.0 Hz).

Example 272
Syntehsis of (E)-3-(2,6-difluoro-4-{4-[2-fluoro-3-(1-methyloxy-3-phenylpropyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1781)

1H-NMR(DMSO-d6) 13.00 (bs, 2H), 7.94-8.06 (m, 3H), 7.65 (d, 1H, J=2.6 Hz), 7.15-7.44 (m, 8H), 4.54-4.58 (m, 1H), 3.20 (s, 3H), 2.61-2.73 (m, 2H), 1.94-2.09 (m, 2H), 1.81(s, 3H).

Example 273
Syntehsis of (E)-3-(2,6-dichloro-4-{4-[2-fluoro-3-(1-methyloxy-3-phenylpropyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1782)

1H-NMR(DMSO-d6) 13.02 (bs, 2H), 8.30(s, 2H), 8.00-8.06 (m, 1H), 7.65 (d, 1H, J=2.6 Hz), 7.16-7.44 (m, 8H), 4.54-4.58 (m, 1H), 3.21 (s, 3H), 2.64-2.74 (m, 2H), 1.96-2.08 (m, 2H), 1.69(s,3H).

Example 274
Syntehsis of (E)-3-(4-{4-[3-(2-ethyl-1-methoxybutyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methylacrylic acid (B1783)

1H-NMR(DMSO-d6) 13.00 (bs, 2H), 7.95-8.05 (m, 3H), 7.65 (d, 1H, J=2.6 Hz), 7.33-7.36 (m, 3H), 4.51 (d, 1H, 6.4 Hz), 3.16 (s, 3H), 1.81(d, 3H, J=1.4 Hz), 1.35-1.60 (m, 3H), 1.24-1.36 (m, 2H), 0.81-0.86 (m, 6H).

Example 275
Syntehsis of (E)-3-(2,6-dichloro-4-{4-[3-(2-ethyloxy-1-methyloxybutyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1784)

1H-NMR(DMSO-d6) 13.01 (bs, 2H), 8.29 (s, 2H), 7.99-8.05 (m, 1H), 7.65 (d, 1H, J=2.6 Hz), 7.40 (s, 1H), 7.34-7.36 (m, 2H), 4.521 (d, 1H, 6.1 Hz), 3.16 (s, 3H), 1.39(s, 3H), 1.38-1.60 (m, 3H), 1.18-1.38 (m, 2H), 0.81-0.86 (m, 6H).

Example 275
Syntehsis of (E)-3-(4-{4-[3-(3-butyloxy-1-methyloxypropyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methylacrylic acid (B1785)

1H-NMR(DMSO-d6) 13.00 (bs, 2H), 94-8.06 (m, 3H), 7.66 (d, 1H, J=2.5 Hz), 7.32-7.42 (m, 3H), 4.68-4.70 (m, 1H), 3.47-3.55 (m, 1H), 3.30-3.38 (m, 3H), 1.85-2.01 (m, 2H), 1.81(s,3H), 1.42-1.50 (m, 2H), 1.27-1.37 (m, 2H), 0.84-0.89 (m, 3H).

Example 277
Syntehsis of (E)-3-(4-{4-[3-(3-butyloxy-1-methyloxypropyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}-2,6-dichlorophenyl)-2-methyl acrylic acid (B1786)

1H-NMR(DMSO-d6) 13.01 (bs, 2H), 8.29 (s, 2H), 8.00-8.06 (m, 1H), 7.65 (d, 1H, J=2.6 Hz), 7.31-7.41 (m, 3H), 4.68-4.73 (m, 1H), 3.47-3.55 (m, 1H), 3.28-3.39 (m, 3H), 1.85-2.01 (m, 2H), 1.69(s,3H), 1.43-1.50 (m, 2H), 1.29-1.34 (m, 2H), 0.84-0.89 (m, 3H).

Example 278
Syntehsis of (E)-3-{4-[4-(4′-t-butyl-2-methyloxybiphenyl-3-yl)thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methylacrylic acid (B1787)

1H-NMR(DMSO-d6) 12.96 (bs, 2H), 8.04-8.07 (m, 1H), 7.96-7.98 (m, 2H), 7.79 (s, 1H), 7.48-7.55 (m, 4H), 7.27-7.34 (m, 3H), 3.31 (s, 3H), 1.81 (s, 3H), 1.34 (s, 9H).

Example 279
Syntehsis of (E)-3-{4-[4-(4′-t-butyl-2-methyloxybiphenyl-3-yl)thiazol-2-ylcarbamoyl}-2,6-dichlorophenyl)-2-methylacrylic acid (B1788)

1H-NMR(DMSO-d6) 12.98 (bs, 2H), 8.30 (s, 2H), 8.03-8.06 (m, 1H), 7.79 (s, 1H), 7.48-7.55 (m, 4H), 7.40 (s, 1H), 7.27-7.35 (m, 2H), 3.31 (s, 3H), 1.69 (s, 3H).

Example 280
Syntehsis of (E)-3-{4-[4-(4′-t-butyl-2-fluorobiphenyl-3-yl)thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methylacrylic acid (B1789)

1H-NMR(DMSO-d6) 13.01 (bs, 2H), 8.06-8.11 (m, 1H), 7.95-8.00 (m, 2H), 7.69 (d, 1H, J=2.6 Hz), 7.34-7.53 (m, 7H), 1.81 (s, 3H), 1.34 (s, 9H).

Example 281
Syntehsis of (E)-3-{4-[4-(4′-t-butyl-2-fluorobiphenyl-3-yl)thiazol-2-ylcarbamoyl}-2,6-dichlorophenyl)-2-methylacrylic acid (B1790)

1H-NMR(DMSO-d6) 13.05 (bs, 2H), 8.30 (s, 2H), 8.06-8.10 (m, 1H), 7.69 (d, 1H, J=2.6 Hz), 7.37-7.53 (m, 7H), 1.69 (s, 3H), 1.34 (s, 9H).

Example 282
Syntehsis of (E)-3-(4-{4-[3-(4-butyloxy-1-methyloxybutyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methylacrylic acid (B1791)

1H-NMR(DMSO-d6) 13.00(bs, 2H), 7.93-8.06(m, 3H), 7.65(d, 1H, J=2.7 Hz), 7.32-7.39(m, 3H), 4.58-4.62(m, 1H), 3.20-3.44(m, 4H), 3.19(s, 3H), 1.22-1.88(m, 11H), 0.85(t, 3H, J=7.2 Hz).

Example 283
Syntehsis of (E)-3-(2,6-difluoro-4-{4-[2-fluoro-3-(1-methyloxy-4-propyloxybutyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1792)

1H-NMR(DMSO-d6) 13.00(bs, 2H), 7.93-8.06(m, 3H), 7.65(d, 1H, J=2.7 Hz), 7.32-7.40(m, 3H), 4.58-4.62(m, 1H), 3.25-3.37(m, 4H), 3.19(s, 3H), 1.41-1.85(m, 9H), 0.83(t, 3H, J=7.2 Hz).

Example 284
Syntehsis of (E)-3-(4-{4-[3-(4-ethyloxy-1-methyloxybutyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methylacrylic acid (B1793)

1H-NMR(DMSO-d6) 13.02(bs, 2H), 7.94-8.07(m, 3H), 7.65(d, 1H, J=2.4 Hz), 7.32-7.40(m, 3H), 4.58-4.63(m, 1H), 3.28-3.40(m, 4H), 3.19(s, 3H), 1.43-1.83(m, 7H), 1.08(t, 3H, J=7.2 Hz).

Example 285
Syntehsis of (E)-3-(2,6-dichloro-4-{4-[3-(4-ethyloxy-1-methyloxybutyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1794)

1H-NMR(DMSO-d6) 13.02(bs, 2H), 8.29(s, 2H), 8.00-8.05(m, 1H), 7.65(d, 1H, J=2.7 Hz), 7.32-7.41(m, 3H), 4.58-4.31(m, 1H), 3.26-3.40(m, 4H), 3.19(s, 3H), 1.40-1.88(m, 7H), 1.08(t, 3H, J=7.2 Hz).

Example 286
Syntehsis of (E)-3-(4-{4-[3-(3,3-dimethylbut-1-ynyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methylacrylic acid (B1795)

1H-NMR(DMSO-d6) 13.01 (bs, 2H), 8.03-8.08 (m, 1H), 7.95-7.98 (m, 2H), 7.72 (d, 1H, J=2.7 Hz), 7.26-7.45 (m, 3H), 1.81 (s, 3H), 1.33 (s, 9H).

Example 287
Syntehsis of (E)-3-(2,6-dichloro-4-{4-[3-(3,3-dimethylbut-1-ynyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1796)

1H-NMR(DMSO-d6) 13.01 (bs, 2H), 8.30 (s, 2H), 8.02-8.08 (m, 1H), 7.72 (d, 1H, J=2.6 Hz), 7.40-7.44 (m, 2H), 7.27-7.32 (m, 1H), 1.69 (s, 3H), 1.37 (s, 9H).

Example 288
Syntehsis of (E)-3-{2,6-difluoro-4-[4-(2-octyloxyphenyl)thiazol-2-ylcarbamoyl]phenyl)-2-methylacrylic acid (B1797)

1H-NMR(DMSO-d6) 12.91(bs, 2H), 7.92-8.00(m, 2H), 7.38-7.51(m, 3H), 7.30-7.37(m, 2H), 7.27(s, 1H), 4.13(t, 2H, J=6.6 Hz), 1.80-1.92(m, 5H), 1.20-1.52(m, 10H), 0.83-0.88(m, 3H).

Example 289
Syntehsis of (E)-3-{2,6-dichloro-4-[4-(2-octyloxyphenyl)thiazol-2-ylcarbamoyl]phenyl)-2-methylacrylic acid (B1798)

1H-NMR(DMSO-d6) 12.97(bs, 2H), 8.28(s, 2H), 7.30-7.50(m, 5H), 7.27(s, 1H), 4.13(t, 2H, J=6.6 Hz), 1.80-1.90(m, 2H), 1.69(d, 3H, J=1.5 Hz), 1.18-1.52(m, 10H), 0.83-0.88(m, 3H).

Example 290
Syntehsis of (E)-3-(2,6-difluoro-4-{4-[2-methyloxy-3-(1-methyloxy-4-propyloxybutyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1799)

1H-NMR(DMSO-d6) 13.00(bs, 2H), 7.90-8.10(m, 3H), 7.73(s, 1H), 7.25-7.34(m, 3H), 4.59-4.63(m, 1H), 3.62(s, 3H), 3.16(s, 3H), 1.81(s, 3H), 1.42-1.76(m, 6H), 0.84(t, 3H, J=7.5 Hz).

Example 291
Syntehsis of (E)-3-(2,6-dichloro-4-{4-[2-methyloxy-3-(1-methyloxy-4-propyloxybutyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1800)

1H-NMR(DMSO-d6) 13.00(bs, 2H), 8.29(s, 2H), 7.86(dd, 1H, J=1.6, 7.5 Hz), 7.70(s, 1H), 7.41(d, 1H, J=0.9 Hz), 7.31(dd, 1H, J=1.8, 7.8 Hz), 7.25(t, 1H, J=7.5 Hz), 4.53-4.58(m, 1H), 3.67-3.74(m, 2H), 3.15(s, 3H), 1.69(s, 3H), 1.20-1.40(m, 19H), 0.83-0.87(m, 3H).

Example 292
Syntehsis of (E)-3-{2,6-difluoro-4-[4-(2-fluoro-3-pent-1-ynylphenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methylacrylic acid (B1801)

1H-NMR(DMSO-d6) 13.01(bs, 2H), 8.05(dt, 1H, J=1.8, 7.8 Hz), 7.92-8.00(m, 2H), 7.71(d, 1H, J=2.7 Hz), 7.43-7.48(m, 1H), 7.34(s, 1H), 7.30(t, 1H, J=7.8 Hz), 1.81(s, 3H), 1.54-1.66(m, 2H), 1.03(d, 3H, J=7.5 Hz).

Example 293
Syntehsis of (E)-3-{2,6-dichloro-4-[4-(2-fluoro-3-pent-1-ynylphenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methylacrylic acid (B1802)

1H-NMR(DMSO-d6) 13.02(bs, 2H), 8.28(s, 2H), 8.05(dt, 1H, J=2.1, 7.8 Hz), 7.66-1.70(m, 1H), 7.38-7.48(m, 2H), 7.30(t, 1H, J=7.8 Hz), 1.69(s, 3H), 1.57-1.64(m, 2H), 1.03(d, 3H, J=7.5 Hz).

Example 294
Syntehsis of (E)-3-{2,6-difluoro-4-[4-(2-fluoro-3-hert-1-ynylphenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methylacrylic acid (B1803)

1H-NMR(DMSO-d6) 13.01(bs, 2H), 8.02-8.10(m, 1H), 7.90-8.00(m, 2H), 7.68(d, 1H, J=3.0 Hz), 7.41-7.48(m, 1H), 7.35(s, 1H), 7.30(t, 1H, J=7.8 Hz), 1.81(s, 3H), 1.56-1.65(m, 2H), 1.30-1.48(m, 4H), 0.91(t, 3H, J=7.2 Hz).

Example 295
Syntehsis of (E)-3-{2,6-dichloro-4-[4-(2-fluoro-3-hert-1-ynylphenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methylacrylic acid (B1804)

1H-NMR(DMSO-d6) 13.02(bs, 2H), 8.28(s, 2H), 8.05(dt, 1H, J=1.8, 7.8 Hz), 7.69(d, 1H, J=2.7 Hz), 7.38-7.48(m, 2H), 7.30(t, 1H, J=7.8 Hz), 1.69(s, 3H), 1.54-1.63(m, 2H), 1.31-1.48(m, 4H), 0.91(d, 3H, J=7.2 Hz).

Example 296
Syntehsis of (E)-3-{4-[4-(3-dec-1-ynyl-2-fluorophenyl)thiazol-2-ylcarbamoyl]-2,6-difluorophenyl}-2-methylacrylic acid (B1805)

1H-NMR(DMSO-d6) 13.02(bs, 2H), 8.05(dt, 1H, J=1.8, 7.8 Hz), 7.92-8.00(m, 2H), 7.68(d, 1H, J=2.7 Hz), 7.42-7.47(m, 1H), 7.34(s, 1H), 7.30(t, 1H, J=7.8 Hz), 1.80(s, 1H), 1.52-1.65(m, 2H), 1.37-1.50(m, 2H), 1.23-1.34(m, 8H), 0.84-0.89(m, 3H).

Example 297
Syntehsis of (E)-3-{2,6-dichloro-4-[4-(3-dec-1-ynyl-2-fluorophenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methylacrylic acid (B1806)

1H-NMR(DMSO-d6) 13.02(bs, 2H), 8.28(s, 2H), 8.02-8.09(m, 1H), 7.68(d, 1H, J=2.4 Hz), 7.38-7.47(m, 2H), 7.29(t, 1H, J=7.8 Hz), 1.69(s, 3H), 1.20-1.62(m, 12H), 0.82-0.90(m, 3H).

Example 296
Syntehsis of (E)-3-(2,6-difluoro-4-{4-[2-fluoro-3-(4-methylpent-1-ynyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1807)

1H-NMR(DMSO-d6) 13.02(bs, 2H), 8.05(dt, 1H, J=2.1, 7.8 Hz), 7.92-8.00(m, 2H), 7.70(d, 1H, J=2.7 Hz), 7.42-7.49(m, 1H), 7.34(s, 1H), 7.30(t, 1H, J=7.5 Hz), 2.41(d, 2H, J=6.3 Hz), 1.86-1.94(m, 1H), 1.80(s, 3H), 1.04(d, 6H, J=6.9 Hz).

Example 299
Syntehsis of (E)-3-(2,6-dichloro-4-{4-[2-fluoro-3-(4-methylpent-1-ynyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1808)

1H-NMR(DMSO-d6) 13.04(bs, 2H), 8.29(s, 2H), 8.05(dt, 1H, J=1.5, 7.8 Hz), 7.70(d, 1H, J=2.7 Hz), 7.38-7.59(m, 2H), 7.30(t, 1H, J=7.8 Hz), 2.42(d, 2H, J=6.3 Hz), 1.83-1.96(m, 1H), 1.69(s, 3H), 1.04(d, 6H, J=6.6 Hz).

Example 300
Syntehsis of (E)-3-{4-[4-(3-cyclohexy-1-enylethynyl-2-fluorophenyl)thiazol-2-ylcarbamoyl]-2,6-difluorophenyl)-2-methylacrylic acid (B1809)

1H-NMR(DMSO-d6) 13.02(bs, 2H), 8.04-8.12(m,1H), 7.92-8.02(m, 2H), 7.72(d, 1H, J=3.0 Hz), 7.44-7.51(m, 1H), 7.27-7.35(m, 2H), 6.26-6.30(m, 1H), 2.10-2.24(m, 4H), 1.81(s, 3H), 1.46-1.69(m, 4H).

Example 301
Syntehsis of (E)-3-{4-[4-(3-cyclohexy-1-enylethynyl-2-fluorophenyl)thiazol-2-ylcarbamoyl]-2,6-difluorophenyl)-2-methyloxyacrylic acid (B1810)

1H-NMR(DMSO-d6) 13.02(bs, 2H), 8.12(dt, 1H, J=1.8, 7.8 Hz), 7.92-8.00(m, 2H), 7.72(d, 1H, J=2.4 Hz), 7.51-7.57(m, 1H), 7.33-7.38(m, 2H), 4.41(s, 2H), 3.71(s, 3H), 1.81(s, 1H).

Example 302
Syntehsis of (E)-3-(2,6-difluoro-4-{4-[2-fluoro-3-(3-propyloxyprop-1-ynyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1811)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 8.13(t, 1H, J=7.5 Hz), 7.96(s, 1H), 7.93(s, 1H), 7.72(s, 1H), 7.52(t, 1H, J=7.5 Hz), 7.40(s, 1H), 7.38(t, 1H, J=7.5 Hz), 4.43(s, 2H), 3.50(t, 2H, J=7.0 Hz), 1.80(s, 3H), 1.50-1.6 (m, 2H), 0.93(t, 3H, J=7.0 Hz).

Example 303
Syntehsis of (E)-3-(2,6-difluoro-4-{4-[2-fluoro-3-(3-isopropyloxyprop-1-ynyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1812)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 8.11(t, 1H, J=7.5 Hz), 7.99(s, 1H), 7.96(s, 1H), 7.72(s, 1H), 7.52(t, 1H, J=7.5 Hz), 7.34(s, 1H), 7.32(t, 1H, J=7.5 Hz), 4.43(s, 2H), 3.70-3.75(m, 1H), 1.80(s, 3H), 1.13 (d, 6H, J=6.0 Hz).

Example 304
Syntehsis of (E)-3-(2,6-difluoro-4-{4-[2-fluoro-3-(3-pentyloxyprop-1-ynyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1813)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 8.10(t, 1H, J=7.5 Hz), 7.99(s, 1H), 7.96(s, 1H), 7.72(s, 1H), 7.52(t, 1H, J=7.5 Hz), 7.34(s, 1H), 7.32(t, 1H, J=7.5 Hz), 4.40(s, 2H), 3.50(t, 2H, J=7.0 Hz), 1.80(s, 3H), 1.50-1.61(m, 2H), 1.20-1.31(m, 4H), 0.88-0.92(m, 3H).

Example 305
Syntehsis of (E)-3-(2,6-dichloro-4-{4-[2-fluoro-3-(3-propyloxyprop-1-ynyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1814)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 8.28(s, 2H), 8.10(t, 1H, J=7.5 Hz), 7.72(s, 1H), 7.52(t, 1H, J=7.5 Hz), 7.40(s, 1H), 7.34(t, 1H, J=7.5 Hz), 4.40(s, 2H), 3.48(t, 2H, J=7.0 Hz), 1.69(s, 3H), 1.50-1.61(m, 2H), 0.93(t, 3H, J=7.0 Hz).

Example 306
Syntehsis of (E)-3-(2,6-dichloro-4-{4-[2-fluoro-3-(3-isopropyloxyprop-1-ynyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1815)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 8.28(s, 2H), 8.10(t, 1H, J=7.5 Hz), 7.72(s, 1H), 7.52(t, 1H, J=7.5 Hz), 7.40(s, 1H), 7.34(t, 1H, J=7.5 Hz), 4.40(s, 2H), 3.70-3.75(m, 1H), 1.69(s, 3H), 1.13(d, 6H, J=6.0 Hz).

Example 307
Syntehsis of (E)-3-(2,6-dichloro-4-{4-[2-fluoro-3-(3-pentyloxyprop-1-ynyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1816)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 8.28(s, 2H), 8.10(t, 1H, J=7.5 Hz), 7.72(s, 1H), 7.44(t, 1H, J=7.5 Hz), 7.40(s, 1H), 7.34(t, 1H, J=7.5 Hz), 4.44(s, 2H), 3.51(t, 2H, J=7.0 Hz), 1.69(s, 3H), 1.50-1.61(m, 2H), 1.20-1.31(m, 4H), 0.93(t, 3H, J=7.0 Hz).

Example 308
Syntehsis of (E)-3-[2,6-dichloro-4-(4-{3-[3-(2,2-dimethylpropyloxy)prop-1-ynyl]-2-fluorophenyl}thiazol-2-ylcarbamoyl)phenyl]-2-methylacrylic acid (B1817)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 8.28(s, 2H), 8.10(t, 1H, J=7.5 Hz), 7.71(s, 1H), 7.50(t, 1H, J=7.5 Hz), 7.40(s, 1H), 7.34(t, 1H, J=7.5 Hz), 4.46(s, 2H), 3.23(s, 2H), 1.69(s, 3H), 0.91(s, 9H).

Example 309
Syntehsis of (E)-3-(4-{4-[3-(5-chloro-pent-1-ynyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methylacrylic acid (B1818)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 8.07(t, 1H, J=7.5 Hz), 7.92-8.00(m, 2H), 7.71(d, 1H, J=3.0 Hz), 7.49(t, 1H, J=7.2 Hz), 7.29-7.34(m, 2H), 3.81(t, 2H, J=6.6 Hz), 2.67(t, 2H, J=7.2 Hz), 1.99-2.08(m, 2H), 1.81(s, 3H).

Example 310
Syntehsis of (E)-3-(2,6-dichloro-4-{4-[3-(5-chloro-pent-1-ynyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1819)

1H-NMR(DMSO-d6) 13.02(bs, 2H), 8.28(s, 2H), 8.06(t, 1H, J=6.9 Hz), 7.70(d, 1H, J=2.4 Hz), 7.48(t, 1H, J=6.3 Hz), 7.40(s, 1H), 7.31(t, 1H, J=7.8. Hz), 3.81(t, 2H, J=6.3 Hz), 2.67(t, 2H, J=6.3 Hz), 1.99-2.08(m, 2H), 1.69(s, 3H).

Example 311
Syntehsis of (E)-3-(4-{4-[3-(5-cyano-pent-1-ynyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methylacrylic acid (B1820)

1H-NMR(DMSO-d6) 8.07(dt, 1H, J=1.5, 7.8 Hz), 7.91-8.00(m, 2H), 7.70(d, 1H, J=2.7 Hz), 7.50(dt, 1H, J=1.5, 6.8 Hz), 7.29-7.34(m, 2H), 2.61-2.69(m, 4H), 1.85-1.94(m, 2H), 1.81(s, 3H).

Example 312
Syntehsis of (Z)-3-{4-[4-(3-dec-1-ynyl-2-fluorophenyl)thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methyloxyacrylic acid (B1821)

1H-NMR(DMSO-d6) 12.99(bs, 1H), 8.04(dt, 1H, J=1.8, 7.8 Hz), 7.88-7.95(m, 2H), 7.69(d, 1H, J=2.7 Hz), 7.44(dt, 1H, J=1.8, 6.6 Hz), 7.29(t, 1H, J=7.8 Hz), 6.64(s, 1H), 3.71(s, 3H), 1.16-1.64(m, 14H), 0.84-0.88(m, 3H).

Example 313
Syntehsis of (E)-3-{2,6-difluoro-4-[4-(2-fluoro-3-pyridyn-3-ylethynylphenyl)thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1822)

1H-NMR(DMSO-d6) 13.00(bs, 2H), 8.81(s, 1H), 8.64(d, 1H, J=3.9 Hz), 8.17(t, 1H, J=7.2 Hz), 8.04(d, 1H, J=7.8 Hz), 7.92-8.10(m, 2H), 7.77(d, 1H, J=2.1 Hz), 7.67(t, 1H, J=6.6 Hz), 7.49-7.53(m, 1H), 7.42(t, 1H, J=7.2 Hz), 7.34(s, 1H), 1.81(s, 3H).

Example 314
Syntehsis of (E)-3-{4-[4-(3-ethynyl-2-fluorophenyl)thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methylacrylic acid (B1823)

1H-NMR(DMSO-d6) 13.02(bs, 2H), 8.12(dt, 1H, J=1.8, 7.5 Hz), 7.92-8.00(m, 2H), 7.72(d, 1H, J=2.7 Hz), 7.55(dt, 1H, J=1.5, 6.9 Hz), 7.32-7.37(m, 2H), 4.57(s, 1H), 1.81(s, 1H).

Example 315
Syntehsis of (Z)-3-(2,6-difluoro-4-{4-[2-fluoro-3-(4-methylpent-1-ynyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methyloxyacrylic acid (B1824)

1H-NMR(DMSO-d6) 12.99(bs, 1H), 8.04(dt, 1H, J=1.5, 7.5 Hz), 7.87-7.95(m, 2H), 7.71(d, 1H, J=2.7 Hz), 7.46(dt, 1H, J=1.8, 7.0 Hz), 7.29(t, 1H, J=7.8 Hz), 6.65(s, 1H), 3.71(s, 3H), 2.41(d, 2H, J=6.6 Hz), 1.85-1.94(m, 1H), 1.04(d, 6H, J=6.6 Hz).

Example 316
Syntehsis of (E)-3-(2,6-difluoro-4-{4-[2-fluoro-3-(3-methylhexyn-1-ynyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1825)

1H-NMR(DMSO-d6) 13.00(bs, 2H), 8.04(dt, 1H, J=1.8, 7.5 Hz), 7.92-8.00(m, 2H), 7.71(d, 1H, J=2.7 Hz), 7.43(dt, 1H, J=1.8, 7.0 Hz), 7.34(s, 1H), 7.29(t, 1H, J=7.8 Hz), 2.68-2.82(m, 1H), 1.81(s, 1H), 1.42-1.64(m, 4H), 1.24(d, 3H, J=6.9 Hz), 0.91-0.96(m, 3H).

Example 317
Syntehsis of (E)-3-(4-{4-[3-(3-cyclopentylprop-1-ynyl)-2-fluorophenyl)thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methylacrylic acid (B1826)

1H-NMR(DMSO-d6) 13.00(bs, 2H), 8.04(dt, 1H, J=1.8, 6.9 Hz), 7.92-8.00(m, 2H), 7.70(d, 1H, J=2.7 Hz), 7.44(dt, 1H, J=1.8, 7.0 Hz), 7.33(s, 1H), 7.30(t, 1H, J=7.8 Hz), 2.05-2.17(m, 1H), 1.76-1.87(m, 5H), 1.48-1.70(m, 4H), 1.29-1.40(m, 2H).

Example 318
Syntehsis of (Z)-3-{4-[4-(3-cyclohexy-1-enylethynyl-2-fluorophenyl)thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methyloxyacrylic acid (B1827)

1H-NMR(DMSO-d6) 12.99(bs, 1H), 8.07(dt, 1H, J=1.5, 7.5 Hz), 7.87-7.95(m, 2H), 7.72(d, 1H, J=2.7 Hz), 7.48(dt, 1H, J=1.8, 6.0 Hz), 7.32(t, 1H, J=7.8 Hz), 6.65(s, 1H), 6.25-6.30(m, 1H), 3.71(s, 3H), 2.10-2.24(m, 4H), 1.54-1.70(m, 4H).

Example 319
Syntehsis of (E)-3-(2,6-dichloro-4-{4-[3-(3,3-dimethylbutyl)-2-fluorophenyl]-5-morpholin-4-ylthiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1828)

1H-NMR(DMSO-d6) 12.82(bs, 1H), 8.23(s, 2H), 7.42(t, 1H, J=7.6 Hz), 7.40(s, 1H), 7.29(t, 1H, J=7.6 Hz), 7.09(d, 1H, J=7.6 Hz ), 3.66-3.72(m, 4H), 2.66-2.78(m, 4H), 2.60-2.70(m, 2H), 1.68(s, 3H), 1.39-1.45(m, 2H), 0.95(s, 9H).

Example 320
Syntehsis of (E)-3-(2,6-difluoro-4-{4-[2-fluoro-3-(1-methyloxyhexyl)phenyl]-5-morpholin-4-ylthiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1829)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 7.92(s, 1H), 7.89(s, 1H), 7.50(t, 1H, J=7.5 Hz), 7.39(t, 1H, J=7.5 Hz), 7.33(s, 1H), 7.28(t, 1H, J=7.5 Hz), 4.51(t, 1H, J=6.5 Hz), 3.66-3.72(m, 4H), 3.16(s, 3H), 2.75-2.86(m, 4H), 1.78(s, 3H), 1.70-1.78(m, 2H,), 1.12-1.38(m, 6H), 0.87-0.90(m, 3H).

Example 321
Syntehsis of (E)-3-(2,6-dichloro-4-{4-[2-fluoro-3-(1-methyloxyhexyl)phenyl]-5-morpholin-4-ylthiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1830)

1H-NMR(DMSO-d6) 12.82(bs, 1H), 8.23(s, 2H), 7.50(t, 1H, J=7.6 Hz), 7.38(s, 1H), 7.36(t, 1H, J=7.6 Hz), 7.28(t, 1H, J=7.6 Hz), 4.51(t, 1H, J=6.5 Hz), 3.66-3.72(m, 4H), 3.16(s, 3H), 2.75-2.86(m, 4H), 1.70-1.78(m, 2H,), 1.68(s, 3H), 1.10-1.38(m, 6H), 0.87-0.90 (m, 3H).

Example 322
Syntehsis of (E)-3-(2,6-dichloro-4-{4-[2-fluoro-3-(3-propyloxypropyl)phenyl]-5-morpholin-4-ylthiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1831)

1H-NMR(DMSO-d6) 12.82(bs, 1H), 8.28(s, 2H), 742(t, 1H, J=7.6 Hz), 7.38(s, 1H), 7.28(t, 1H, J=7.6 Hz), 7.17(t, 1H, J=7.6 Hz), 3.75-3.89(m, 4H), 3.33-3.40(m, 4H), 2.75-2.86(m, 4H), 2.74(t, 1H, J=7.0 Hz), 1.70-1.78(m, 2H), 1.68(s, 3H), 1.20-1.30(m, 2H), 0.87(t, 3H, J=7.0 Hz).

Example 323
Syntehsis of (E)-3-(4-{4-[3-(3-dimethylamino-prop-1-ynyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methylacrylic acid (B1832)

1H-NMR(DMSO-d6) 13.01(bs, 2H), 8.08(dt, 1H, J=1.8, 7.5H), 7.72(d, 1H, J=2.4 Hz), 7.51(dt, 1H, J=1.8, 7.2H), 7.30-7.54(m, 2H), 3.56(s, 2H), 2.29(s, 6H), 1.81 (s, 3H).

Example 324
Syntehsis of (E)-3-[2,6-dichloro-4-(4-{3-[3-(2,2-dimethylpropyloxy)propyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1833)

1H-NMR(CDCl3-d6) 8.31(s, 2H), 7.66(s, 1H), 7.46-7.53(m, 2H), 7.24-7.30(m, 1H), 7.17(t, 1H J=7.8 Hz), 3.59(s, 3H), 3.46-3.52(m, 2H), 3.08(s, 2H), 2.76-2.84(m, 2H), 1.92-1.98(m, 2H), 1.87(s, 3H), 0.94(s, 9H).

Example 325
Syntehsis of (E)-3-(4-{4-[3-(2-butyloxyethyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methylacrylic acid (B1834)

1H-NMR(DMSO-d6) 12.96 (bs, 2H), 7.95-7.98 (m, 2H), 7.86-7.88 (m, 1H), 7.73 (s, 1H), 7.34 (s, 1H), 7.27-7.29 (m, 1H), 7.14-7.19 (m, 1H), 3.59-3.65 (m, 5H), 3.40 (t, 2H, J=6.6 Hz), 2.91 (t, 2H, J=6.9 Hz), 1.81 (s, 3H), 1.42-1.50 (m, 2H), 1.26-1.34 (m, 2H),0.86 (t, 3H, J=7.0 Hz).

Example 326
Syntehsis of (Z)-3-(4-{4-[3-(2-butyloxyethyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methyloxyacrylic acid (B1835)

1H-NMR(DMSO-d6) 12.92 (bs, 2H), 7.85-7.93 (m, 3H), 7.72 (s, 1H), 7.26-7.29 (m, 1H), 7.13-7.18 (m, 1H), 6.66 (s, 1H), 3.71 (s, 3H), 3.59-3.65 (m, 5H), 3.41 (t, 2H, J=6.6 Hz), 2.91 (t, 2H, J=6.9 Hz), 1.43-1.50 (m, 2H), 1.27-1.34 (m, 2H), 0.87 (t, 3H, J=7.0 Hz).

Example 327
Syntehsis of (E)-3-(4-{4-[3-(2-butyloxyethyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}-2,6-dichlorophenyl)-2-methylacrylic acid (B1836)

1H-NMR(DMSO-d6) 12.97 (bs, 2H), 8,26 (s, 2H), 7.85-7.89 (m, 1H), 7.72 (s, 1H), 7.40 (s, 1H), 7.26-7.29 (m, 1H), 7.13-7.19 (m, 1H), 3.59-3.65 (m, 5H), 3.41 (t, 2H, J=6.6 Hz), 2.91 (t, 2H, J=6.9 Hz), 1.69 (s, 3H), 1.43-1.50 (m, 2H), 1.27-1.34 (m, 2H), 0.86 (t, 3H, J=7.0 Hz).

Example 328
Syntehsis of (Z)-3-(4-{4-[3-(2-butyloxyethyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}-2,6-dichlorophenyl)-2-methyloxyacrylic acid (B1837)

1H-NMR(DMSO-d6) 12.94 (bs, 2H), 8,24 (s, 2H), 7.85-7.87 (m, 1H), 7.71 (s, 1H), 7.26-7.29 (m, 1H), 7.13-7.18 (m, 1H), 6.73 (s, 1H), 3.59-3.65 (m, 5H), 3.41 (t, 2H, J=6.6 Hz), 3.20 (s, 3H), 2.91 (t, 2H, J=6.9 Hz), 1.43-1.50 (m, 2H), 1.27-1.34 (m, 2H), 0.87 (t, 3H, J=7.0 Hz).

Example 329
Syntehsis of (E)-3-(2,6-difluoro-4-{4-[2-methyloxy-3-(2-propyloxyethyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1838)

1H-NMR(DMSO-d6) 12.96 (bs, 2H), 7.95-7.97 (m, 2H), 7.85-7.89 (m, 1H), 7.72 (s, 1H), 7.34 (s, 1H), 7.26-7.29 (m, 1H), 7.14-7.19 (m, 1H), 3.60-3.65 (m, 5H), 3.70 (t, 2H, J=6.6 Hz), 2.91 (t, 2H, J=6.9 Hz), 1.81 (s, 3H), 1.45-1.52 (m, 2H), 0.85 (t, 3H, J=7.5 Hz).

Example 330
Syntehsis of (E)-3-(2,6-dichloro-4-{4-[2-methyloxy-3-(2-propyloxyethyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1839)

1H-NMR(DMSO-d6) 12.98 (bs, 2H), 8.29 (s, 2H), 7.85-7.88 (m, 1H), 7.72 (s, 1H), 7.41 (s, 1H), 7.27-7.30 (m, 1H), 7.14-7.19 (m, 1H), 3.60-3.66 (m, 5H), 3.37 (t, 2H, J=6.6 Hz), 2.91(t, 2H, J=7.0 Hz), 1.69 (s, 3H), 1.48-1.54 (m, 2H), 0.85 (t, 3H, J=7.5 Hz).

Example 331
Syntehsis of (Z)-3-(2,6-dichloro-4-{4-[2-methyloxy-3-(2-propyloxyethyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methyloxyacrylic acid (B1840)

1H-NMR(DMSO-d6) 13.52 (bs, 1H), 12.98 (bs, 1H), 8.25 (s, 2H), 7.85-7.88 (m, 1H), 7.72 (s, 1H), 7.26-7.30 (m, 1H), 7.14-7.19 (m, 1H), 6.74 (s, 1H), 3.60-3.66 (m, 8H), 3, 70 (t, 2H, J=6.6 Hz), 2.91(t, 2H, J=7.0 Hz), 1.48-1.54 (m, 2H), 0.85 (t, 3H, J=7.5 Hz).

Example 332
Syntehsis of (E)-3-{4-[4-(3-butyloxy-2-fluorophenyl)thiazol-2-ylcarbamoyl]-2,6-difluorophenyl}-2-methylacrylic acid (B1841)

1H-NMR(DMSO-d6) 13.00 (bs, 2H), 7.95-7.98 (m, 2H), 7.60-7.65 (m, 2H), 7.40 (s, 1H), 7.14-7.24 (m, 2H), 4.09 (t, 2H, J=6.6 Hz), 1.80 (s, 3H), 1.70-1.77 (m, 2H), 1.43-1.51 (m, 2H), 0.97 (t, 3H, J=7.5 Hz)

Example 333
Syntehsis of (E)-3-(2,6-difluoro-4-{4-[2-fluoro-3-(1-methyloxybutyl)phenyl]-5-methyloxythiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1842)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 7.93(s, 1H), 7.90(s, 1H), 7.50(t, 1H, J=7.5 Hz), 7.28-7.38(m, 3H), 4.53(t, 1H, J=6.5 Hz), 3.95(s, 3H), 3.17(s, 3H), 1.79(s, 3H), 1.50-1.78(m, 2H,), 1.20-1.30(m, 2H), 0.87(t, 3H, J=7.0 Hz).

Example 334
Syntehsis of (E)-3-(2,6-dichloro-4-{4-[2-fluoro-3-(1-methyloxybutyl)phenyl]-5-methyloxythiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1843)

1H-NMR(DMSO-d6) 12.82(bs, 1H), 8.28(s, 2H), 746(t, 1H, J=7.6 Hz), 7.38(s, 1H), 7.34(t, 1H, J=7.6 Hz), 7.28(t, 1H, J=7.6 Hz), 4.58(t, 1H, J=6.5 Hz), 3.95(s, 3H), 3.17(s, 3H), 1.69(s, 3H), 1.50-1.78(m, 2H), 1.20-1.30(m, 2H), 0.87(t, 3H, J=7.0 Hz).

Example 335
Syntehsis of (Z)-3-(2,6-dichloro-4-{4-[2-fluoro-3-(3-isopropyloxy-1-methyloxypropyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methyloxyacrylic acid (B1844)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 8.25(s, 2H), 8.06(t, 1H, J=7.5 Hz), 7.64(s, 1H), 7.30-7.40(m, 2H), 6.72(s, 1H), 4.72(t, 1H, J=6.5 Hz), 3.61(s, 3H), 3.50-3.58(m, 1H), 3.35-3.42(m, 2H), 3.17(s, 3H), 1.80-1.99(m, 2H), 1.05(d, 6H, J=6.0 Hz).

Example 336
Syntehsis of (Z)-3-(2,6-dichloro-4-{4-[2-fluoro-3-(1-methyloxybutyl)phenyl]-5-methyloxythiazol-2-ylcarbamoyl}phenyl)-2-methyloxyacrylic acid (B1845)

1H-NMR(DMSO-d6) 12.82(bs, 1H), 8.25(s, 2H), 746(t, 1H, J=7.6 Hz), 7.34(t, 1H, J=7.6 Hz), 7.28(t, 1H, J=7.6 Hz), 6.72(s, 1H), 4.53(t, 1H, J=6.5 Hz), 3.9 (s, 3H), 3.60(s, 3H), 3.17(s, 3H), 1.50-1.7 (m, 2H), 1.20-1.30(m, 2H), 0.87(t, 3H, J=7.0 Hz).

Example 337
Syntehsis of (E)-3-(4-{4-[3-(3,3-dimethylbutyl)phenyl]-5-methyloxythiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methylacrylic acid (B1846)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 7.97(s, 1H), 7.96 (s, 1H), 7.77 (s, 1H), 7.75 (t, 1H, J=7.5), 7.38 (s, 1H), 7.12 (t, 1H, J=7.5), 3.99 (s, 3H), 2.50-2.60 (m, 2H), 1.78 (s, 3H), 1.39-1.45 (m, 2H), 0.95 (s, 9H).

Example 338
Syntehsis of (E)-3-(2,6-dichloro-4-{4-[3-(3,3-dimethylbutyl)phenyl]-5-methyloxythiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methylacrylic acid (B1847)

1H-NMR(DMSO-d6) 12.82(bs, 1H), 8.28(s, 2H), 7.77(s, 1H), 7.74(t, 1H, J=7.6 Hz), 7.41(s, 1H), 7.32(t, 1H, J=7.6 Hz), 4.05(s, 3H), 2.50-2.60(m, 2H), 1.68(s, 3H), 1.39-1.45(m, 2H), 0.95(s, 9H).

Example 339
Syntehsis of (E)-3-[4-(4-{3-[3-(2-ethylbutyloxy)propyl]-2-methyloxyphenyl}thiazol-2-ylcarbamoyl)-2,6-difluorophenyl]-2-methylacrylic acid (B1848)

1H-NMR(CDCl3-d6) 7.90(s, 1H), 7.88(s, 1H), 7.58(s, 1H), 7.45-7.50(m, 2H), 7.25-7.28(m, 1H), 7.17(t, 1H, J=7.2 Hz), 3.57(s, 3H), 3.49(t, 2H, J=6.0 Hz), 3.33(d, 2H, J=5.4 Hz), 2.76-2.84(m, 2H), 1.90-2.11(m, 5H), 1.30-1.50(m, 5H), 0.90(t, 6H, J=7.2 Hz).

Example 340
Syntehsis of (E)-3-[2,6-dicholoro-4-(4-{3-[3-(2-ethylbutyloxy)propyl]-2-methyloxyphenyl}thiazol-2-ylcarbamoyl)phenyl]-2-methylacrylic acid (B1849)

1H-NMR(CDCl3-d6) 8.33(s, 2H), 7.65(s, 1H), 7.46-7.52(m, 2H), 2.25-7.28(m, 1H), 7.17(t, 1H, J=7.8 Hz), 3.58(s, 3H), 3.47(t, 2H, J=6 Hz), 3.32(d, 2H, J=5.7 Hz), 2.76-2.82(m, 2H), 1.90-2.00(m, 2H), 1.86(bs, 3H), 1.31-1.50(m, 5H), 0.89(t, 6H, J=7.5 Hz).

Example 341
Syntehsis of (Z)-3-[4-(4-{3-[3-(2-ethylbutyloxy)propyl]-2-methyloxyphenyl}thiazol-2-ylcarbamoyl)-2,6-diflulorophenyl]-2-methyloxyacrylic acid (B1850)

1H-NMR(CDCl3-d6) 7.82(s, 1H), 7.79(s, 1H), 7.40-7.50(m, 2H), 7.25-7.26(m, 1H), 7.17(t, 1H, J=7.5 Hz), 6.92(s, 1H), 3.90(s, 3H), 3.48(t, 2H, J=6.3 Hz), 3.32(d, 2H, J=5.7 Hz), 2.76-2.83(m, 2H), 1.91-2.05(m, 2H), 1.31-1.52(m, 5H), 0.90(t, 6H, J=7.5 Hz).

Example 342
Syntehsis of (E)-3-[2,6-difluoro-4-(4-{2-methyloxy-3-[3-(3-methylbutyloxy)propyl]phenyl}thiazol-2-ylcarbamoyl)phenyl]-2-methylacrylic acid (B1851)

1H-NMR(CDCl3-d6) 7.91(s, 1H), 7.88(s, 1H), 7.57(bs, 1H), 7.47-7.52(m, 1H), 7.47(s, 1H), 7.25-7.30(m, 1H), 7.18(t, 1H, J=7.5 Hz), 3.58(s, 3H), 3.44-3.52(m, 4H), 2.80(t, 2H, J=8.7 Hz), 1.91-2.00(m, 5H), 1.68-1.78(M, 1H), 1.49(q, 2H, J=13.8, 6.9 Hz), 0.92(d, 6H, J=6.3 Hz).

Example 343
Syntehsis of (E)-3-[2,6-dichloro-4-(4-{2-methyloxy-3-[3-(3-methylbutyloxy)propyl]phenyl}thiazol-2-ylcarbamoyl)phenyl]-2-methylacrylic acid (B1852)

1H-NMR(CDCl3-d6) 8.31(s, 2H), 7.65(s, 1H), 7.50(dd, 1H, J=7.8, 1.5 Hz), 7.46(s, 1H), 7.24-7.28(m, 1H), 7.16(t, 1H, J=7.8 Hz), 3.58(s, 3H), 3.43-3.51(m, 4H), 2.76-2.82(m, 2H), 1.85-2.05(m, 2H), 1.86(s, 3H), 1.65-1.80(m, 1H), 1.49(t, 2H, J=13.5, 6.6 Hz), 0.92(d, 6H, J=6.9 Hz).

Example 344
Syntehsis of (Z)-3-[2,6-difluoro-4-(4-{2-methyloxy-3-[3-(3-methylbutyloxy)propyl]phenyl}thiazol-2-ylcarbamoyl)phenyl]-2-methyloxyacrylic acid (B1853)

1H-NMR(CDCl3-d6) 7.84(s, 1H), 7.81(s, 1H), 7.49(d, 1H, J=8.1 Hz), 7.46(s, 1H), 7.29(d, 1H, J=7.5 Hz), 7.18(t, 1H, J=7.5 Hz), 6.91(s, 1H), 3.90(s, 3H), 3.59(s, 3H), 2.40-3.52(m, 4H), 2.80(t, 2H, J=8.1 Hz), 1.90-2.05(m, 2H), 1.65-1.78(m, 1H), 1.49(q, 2H, J=13.5, 6.6 Hz), 0.92(d, 6H, J=6.3 Hz).

Example 345
Syntehsis of (E)-3-(4-{4-[3-(3-cyclobutylmethyloxypropyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methylacrylic acid (B1854)

1H-NMR(CDCl3-d6) 7.91(s, 1H), 7.88(s, 1H), 7.58(s, 1H), 7.49(dd, 1H, J=7.5, 1.5 Hz), 7.46(s, 1H), 7.25-7.29(m, 1H), 7.18(t, 1H, J=7.5 Hz), 3.58(s, 3H), 3.50(t, 2H, J=6.3 Hz), 3.43(d, 2H, J=6.9 Hz), 2.76-2.82(m, 2H), 2.54-2.64(m, 1H), 1.72-1.21(m, 11H).

Example 346
Syntehsis of (E)-3-(2,6-dichloro-4-{4-[3-(3-cyclobutylmethyloxypropyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1855)

1H-NMR(CDCl3-d6) 8.32(s, 2H), 7.66(s, 1H), 7.49(d, 1H, J=6.6 Hz), 7.46(s, 1H), 7.24-7.26(m, 1H), 7.16(t, 1H, J=7.5 Hz), 3.57(s, 3H), 3.49(t, 2H, 6.3 Hz), 3.42(d, 2H, J=6.6 Hz), 2.78(t, 2H, J=7.8 Hz), 2.52-2.64(m, 1H), 2.01-2.12(m, 2H), 1.70-2.00(m, 9H).

Example 347
Syntehsis of (Z)-3-(4-{4-[3-(3-cyclobutylmethyloxypropyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methyloxyacrylic acid (B1856)

1H-NMR(CDCl3-d6) 7.82(s, 1H), 7.79(s, 1H), 7.44-7.50(m, 2H), 7.25-7.30(m, 1H), 7.17(t, 1H, J=7.5 Hz), 6.92(s, 1H), 3.91(s, 3H), 3.57(s, 3H), 3.50(t, 2H, J=6.3 Hz), 3.43(d, 2H, J=6.9 Hz), 2.79(t, 2H, J=7.8 Hz), 2.53-2.66(m, 1H), 1.72-2.13(m, 8H).

Example 348
Syntehsis of (Z)-3-(2,6-dichloro-4-{4-[3-(3-cyclobutylmethyloxypropyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methyloxyacrylic acid (B1857)

1H-NMR(CDCl3-d6) 8.25(s, 2H), 7.47(d, 1H, J=7.8 Hz), 7.44(s, 1H), 7.24-7.26(m, 1H), 7.16(t, 1H, J=7.5 Hz), 7.02(s, 1H), 3.73(s, 3H), 3.57(s, 3H), 3.49(t, 2H, J=6.0 Hz), 3.42(d, 2H, J=6.6 Hz), 2.78(t, 2H, J=8.1 Hz), 2.53-2.64(m, 1H), 1.71-2.14(m, 8H).

Example 349
Syntehsis of (E)-3-(2,6-difluoro-4-{4-[2-fluoro-3-(1-methyloxyhexyl)phenyl]-5-methyoxythiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1858)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 7.93(s, 1H), 7.90(s, 1H), 7.48(t, 1H, J=7.5 Hz), 7.28-7.38(m, 3H), 4.51(t, 1H, J=6.5 Hz), 3.95(s, 3H), 3.17(s, 3H), 1.79(s, 3H), 1.50-1.78(m, 2H), 1.20-1.30(m, 6H), 0.87-0.90(m, 3H).

Example 350
Syntehsis of (E)-3-(2,6-dichloro-4-{4-[2-fluoro-3-(1-methyloxyhexyl)phenyl]-5-methyoxythiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1859)

1H-NMR(DMSO-d6) 12.82(bs, 1H), 8.28(s, 2H), 7.46(t, 1H, J=7.6 Hz), 7.38(s, 1H), 7.34(t, 1H, J=7.6 Hz), 7.28(t, 1H, J=7.6 Hz), 4.51(t, 1H, J=6.5 Hz), 3.95(s, 3H), 3.17(s, 3H), 1.50-1.78(m, 2H), 1.69(s, 3H), 1.20-1.30(m, 6H), 0.87-0.90(m, 3H).

Example 351
Syntehsis of (Z)-3-(2,6-difluoro-4-{4-[2-fluoro-3-(1-methyloxyhexyl)phenyl]-5-methyoxythiazol-2-ylcarbamoyl}phenyl)-2-methyloxyacrylic acid (B1860)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 7.90(s, 1H), 7.88(s, 1H), 7.48(t, 1H, J=7.5 Hz), 7.36(t, 1H, J=7.5 Hz), 7.28(t, 1H, J=7.5 Hz), 6.65(s, 1H), 4.51(t, 1H, J=6.5 Hz), 3.95(s, 3H), 3.70(s, 3H), 3.17(s, 3H), 1.50-1.78(m, 2H,), 1.20-1.30(m, 6H), 0.87-0.90(m, 3H).

Example 352
Syntehsis of (Z)-3-(2,6-dichloro-4-{4-[2-fluoro-3-(1-methyloxyhexyl)phenyl]-5-methyoxythiazol-2-ylcarbamoyl}phenyl)-2-methyloxyacrylic acid (B1861)

1H-NMR(DMSO-d6) 12.82(bs, 1H), 8.20(s, 2H), 7.46(t, 1H, J=7.6 Hz), 7.34(t, 1H, J=7.6 Hz), 7.28(t, 1H, J=7.6 Hz), 6.65(s, 1H), 4.51(t, 1H, J=6.5 Hz), 3.95(s, 3H), 3.60(s, 3H), 3.17(s, 3H), 1.50-1.78(m, 2H), 1.20-1.30(m, 6H), 0.87-0.90(m, 3H).

Example 353
Syntehsis of (E)-3-(2,6-difluoro-4-{5-methyloxy-4-[3-(3-propyloxypropyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1862)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 7.93(s, 1H), 7.90(s, 1H), 7.77(s, 1H), 7.76(d, 1H, J=7.5 Hz), 7.34(s, 1H), 7.33(t, 1H, J=7.6 Hz), 7.11(t, 1H, J=7.6 Hz), 4.05(s, 3H), 3.33-3.40(m, 4H), 2.74(t, 1H, J=7.0 Hz), 1.75-1.85(m, 2H), 1.79(s, 3H), 1.45-1.55(m, 2H), 0.87(t, 3H, J=7.0 Hz).

Example 354
Syntehsis of (E)-3-(2,6-dichloro-4-{5-methyloxy-4-[3-(3-propyloxypropyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1863)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 8.28(s, 2H), 7.77(s, 1H), 7.76(d, 1H, J=7.5 Hz), 7.39(s, 1H), 7.33(t, 1H, J=7.6 Hz), 7.11(t, 1H, J=7.6 Hz), 4.05(s, 3H), 3.33-3.40(m, 4H), 2.74(t, 1H, J=7.0 Hz), 1.75-1.85(m, 2H), 1.68(s, 3H), 1.45-1.55(m, 2H), 0.87(t, 3H, J=7.0 Hz).

Example 355
Syntehsis of (Z)-3-(2,6-difluoro-4-{5-methyloxy-4-[3-(3-propyloxypropyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methyloxyacrylic acid (B1864)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 7.88(s, 1H), 7.85(s, 1H), 7.77(s, 1H), 7.76(d, 1H, J=7.5 Hz), 7.33(t, 1H, J=7.6 Hz), 7.11(t, 1H, J=7.6 Hz), 6.63(s, 1H), 4.05(s, 3H), 3.79(s, 3H), 3.33-3.40(m, 4H), 2.74(t, 1H, J=7.0 Hz), 1.75-1.85(m, 2H), 1.45-1.55 (m, 2H), 0.87(t, 3H, J=7.0 Hz).

Example 356
Syntehsis of (Z)-3-(2,6-dichloro-4-{5-methyloxy-4-[3-(3-propyloxypropyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methyloxyacrylic acid (B1865)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 8.28(s, 2H), 7.77(s, 1H), 7.76(d, 1H, J=7.5 Hz), 7.33(t, 1H, J=7.6 Hz), 7.11(t, 1H, J=7.6 Hz), 6.63(s, 1H), 4.05(s, 3H), 3.70(s, 3H), 3.33-3.40(m, 4H), 2.64(t, 1H, J=7.0 Hz), 1.75-1.85(m, 2H), 1.45-1.55(m, 2H), 0.87(t, 3H, J=7.0 Hz).

Example 357
Synthesis of (E)-3-(4-{4-[3-(3-ethyloxy-1-methyloxypropyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methylacrylic acid (B1866)

1H-NMR(DMSO-d6) 13.01(bs, 2H), 8.03(dt, 1H, J=2.4, 7.5 Hz), 7.93-7.99(m, 2H), 7.66(d, 1H, J=2.7 Hz), 7.32-7.41(m, 3H), 4.68-4.73(m, 1H), 3.47-3.54(m, 1H), 3.36-3.43(m, 2H), 3.18(s, 3H), 1.85-2.02(m, 2H), 1.81(s, 3H), 1.09(t, 3H, J=6.9 Hz).

Example 358
Synthesis of (E)-3-(2,6-dichloro-4-{4-[3-(3-ethyloxy-1-methyloxypropyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1867)

1H-NMR(DMSO-d6) 13.00(bs, 2H), 8.27(s, 2H), 8.01(dt, 1H, J=3.0, 6.6 Hz), 7.63(d, 1H, J=2.4 Hz), 7.30-7.39(m, 3H), 4.66-4.71(m, 1H), 3.45-3.53(m, 1H), 3.16(s, 3H), 1.83-2.00(m, 2H), 1.67(s, 3H), 1.07(t, 3H, J=6.9 Hz).

Example 359
Synthesis of (E)-3-{4-[4-(3-benzyloxy-2-methyloxyphenyl)thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methylacrylic acid (B11868)

1H-NMR(DMSO-d6) 12.95 (bs, 2H), 7.95-7.98 (m, 2H), 7.77 (s, 1H), 7.66-7.69 (m, 1H), 7.34-7.54 (m, 6H), 7.13-7.15 (m, 2H), 5.20 (s, 2H), 3.82 (s, 3H), 1.81 (s, 3H).

Example 360
Synthesis of (Z)-3-{4-[4-(3-benzyloxy-2-methyloxyphenyl)thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methyloxyacrylic acid (B1869)

1H-NMR(DMSO-d6) 12.89 (bs, 2H), 7.89-7.92 (m, 2H), 7.76 (s, 1H), 7.66-7.69 (m, 1H), 7.34-7.53 (m, 5H), 7.13-7.15 (m, 2H), 6.66 (s, 1H), 5.19 (s, 2H), 3.82 (s, 3H), 3.71 (s, 3H).

Example 361
Synthesis of (E)-3-{4-[4-(3-benzyloxy-2-methyloxyphenyl)thiazol-2-ylcarbamoyl}-2,6-dichlorophenyl)-2-methylacrylic acid (B1870)

1H-NMR(DMSO-d6) 12.95 (bs, 2H), 8.29 (s, 2H), 7.76 (s, 1H), 7.66-7.69 (m, 1H), 7.35-7.54 (m, 6H), 7.13-7.15 (m, 2H), 5.20 (s, 2H), 3.82 (s, 3H), 1.69 (s, 3H).

Example 362
Synthesis of (Z)-3-{4-[4-(3-benzyloxy-2-methyloxyphenyl)thiazol-2-ylcarbamoyl}-2,6-dichlorophenyl)-2-methyloxyacrylic acid (B1871)

1H-NMR(DMSO-d6) 12.92 (bs, 2H), 8.24 (s, 2H), 7.76 (s, 1H), 7.66-7.69 (m, 1H), 7.35-7.54 (m, 5H), 7.13-7.15 (m, 2H), 6.74 (s, 2H), 5.20 (s, 1H), 3.82 (s, 3H), 3.61 (s, 3H).

Example 363
Synthesis of (E)-3-(4-{4-[3-(4-chlorobutyloxy)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methylacrylic acid (B1872)

1H-NMR(DMSO-d6) 12.93 (bs, 2H), 7.95-7.97 (m, 2H), 7.75 (s, 1H), 7.64-7.67 (m, 1H), 7.33 (s, 1H), 7.11-7.16 (m, 1H), 7.03-7.06 (m, 1H), 4.06-4.10 (m, 2H,), 3.80 (s, 3H), 3.74-3.78 (m, 2H), 1.93 (bs, 4H), 1.81 (s, 3H).

Example 364
Synthesis of (E)-3-(4-{4-[3-(4-chlorobutyloxy)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methyloxyacrylic acid (B1873)

1H-NMR(DMSO-d6) 12.89 (bs, 2H), 7.89-7.92 (m, 2H), 7.75 (s, 1H), 7.65-7.67 (m, 1H), 7.11-7.16 (m, 1H), 7.03-7.06 (m, 1H), 6.67 (s, 1H), 4.06-4.10 (m, 2H,), 3.80 (s, 3H), 3.74-3.78 (m, 2H), 3.71 (s, 3H), 1.93 (bs, 4H).

Example 365
Synthesis of (Z)-3-(2,6-dichloro-4-{4-[3-(4-chlorobutyloxy)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methyloxyacrylic acid (B1874)

1H-NMR(DMSO-d6) 12.96 (bs, 2H), 8.29 (s, 2H), 7.75 (s, 1H), 7.65-7.67 (m, 1H), 7.40 (s, 1H), 7.11-7.16 (m, 1H), 7.03-7.06 (m, 1H), 4.06-4.10 (m, 2H,), 3.80 (s, 3H), 3.74-3.78 (m, 2H), 1.93 (bs, 4H), 1.69 (s, 3H).

Example 366
Synthesis of (E)-3-(2,6-difluoro-4-{4-[2-methyloxy-3-(3-methyloxypropylphenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1875)

1H-NMR(CDCl3-d6) 7.90(s, 1H), 7.88(s, 1H), 7.58(s, 1H), 7.49(d, 1H, J=6.3 Hz), 7.46(s, 1H), 7.25-7.28(m, 1H), 7.18(t, 1H, J=7.5 Hz), 3.57(s, 3H), 3.47(t, 2H, J=6.3 Hz), 3.37(s, 3H), 2.79(t, 2H, J=8.1 Hz), 1.93-2.00(m, 5H).

Example 367
Synthesis of (E)-3-(2,6-dichloro-4-{4-[2-methyloxy-3-(3-methyloxypropylphenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1876)

1H-NMR(CDCl3-d6) 8.32(s, 2H), 7.66(s, 1H), 7.45-7.51(m, 2H), 7.24-7.27(m, 1H), 7.17(t, 1H, J=7.5 Hz), 3.57(s, 3H), 3.46(t, 2H, J=6.3 Hz), 3.37(s, 3H), 2.78(t, 2H, J=8.7 Hz), 1.90-2.04(m, 2H), 1.87(s, 3H).

Example 368
Synthesis of (E)-3-(2,6-difluoro-4-{4-[3-(3-isobuyloxypropyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1877)

1H-NMR(CDCl3-d6) 7.90(s, 1H), 7.87(s, 1H), 7.58(s, 1H), 7.45-7.52(m, 2H), 7.24-7.30(m, 1H), 7.17(t, 1H, J=7.5 Hz), 3.57(s, 3H), 3.50(t, 2H, 6.3 Hz), 3.21(d, 2H, J=6.6 Hz), 2.80(t, 2H, 8.7 Hz), 1.84-2.03(m, 6H), 0.93(d, 6H, J=6.3 Hz).

Example 369
Synthesis of (E)-3-(2,6-dichloro-4-{4-[3-(3-isobuyloxypropyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1878)

1H-NMR(CDCl3-d6) 8.32(s, 2H), 7.66(s, 1H), 7.45(d, 1H, J=7.2 Hz), 7.46(s, 1H), 7.24-7.28(m, 1H), 7.16(t, 1H, J=7.5 Hz), 3.57(s, 3H), 3.49(t, 2H, J=6.0 Hz), 3.20(d, 2H, J=6.6 Hz), 2.80(t, 2H, J=8.4 Hz), 1.83-2.04(m, 6H), 0.92(d, 6H, J=6.3 Hz).

Example 370
Synthesis of (Z)-3-(2,6-difluoro-4-{4-[3-(3-isobuyloxypropyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methyloxyacrylic acid (B1879)

1H-NMR(CDCl3-d6) 7.80(s, 1H), 7.78(s, 1H), 7.46(dd, 1H, J=7.8, 2.1 Hz), 7.44(s, 1H), 7.25-7.32(m, 1H), 7.17(t, 1H, J=7.5 Hz), 6.92(s, 1H), 3.91(s, 3H), 3.57(s, 3H), 3.50(t, 2H, J=6.3 Hz), 3.21(d, 2H, J=6.6 Hz), 2.80(t, 2H, J=8.7 Hz), 1.83-2.01(m, 3H), 0.93(d, 6H, J=6.3 Hz).

Example 371
Synthesis of (Z)-3-(2,6-dichloro-4-{4-[3-(3-isobuyloxypropyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methyloxyacrylic acid (B1880)

1H-NMR(CDCl3-d6) 8.25(s, 2H), 7.47(dd, 1H, J=7.8, 1.8 Hz), 7.44(s, 1H), 7.24-7.28(m, 1H), 7.16(t, 1H, J=7.5 Hz), 7.03(s, 1H), 3.73(s, 3H), 3.57(s, 3H), 3.49(t, 2H, J=6.3 Hz), 3.20(d, 2H, J=6.9 Hz), 2.79(t, 2H, J=8.4 Hz), 1.83-2.00(m, 3H), 0.92(d, 6H, J=6.9 Hz).

Example 372
Synthesis of (E)-3-(2,6-difluoro-4-{4-[2-methyloxy-3-(3-propyloxymethyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1881)

1H-NMR(DMSO-d6) 12.95(bs, 2H), 7.93-7.97(m, 3H), 7.72(s, 1H), 7.32-7.38(m, 2H), 7.22(t, 1H, J=7.5 Hz), 4.55(s, 2H), 3.64(s, 3H), 3.45(t, 2H, J=6.6 Hz), 1.79(d, 3H, J=1.5 Hz), 1.54-1.61(m, 2H), 0.89(t, 3H, J=7.2 Hz).

Example 373
Synthesis of (E)-3-(2,6-dichloro-4-{4-[2-methyloxy-3-(3-propyloxymethyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B13882)

1H-NMR(DMSO-d6) 12.95(bs, 2H), 8.27(s, 2H), 7.94-7.97(m, 1H), 7.71(s, 1H), 7.36-7.38(m, 2H), 7.22(t, 1H, J=7.5 Hz), 4.55(s, 2H), 3.64(s, 3H), 3.45(t, 2H, J=6.6 Hz), 1.67(s, 3H), 1.54-1.61(m, 2H), 0.89(t, 3H, J=7.3 Hz).

Example 374
Synthesis of (Z)-3-(2,6-dichloro-4-{4-[2-methyloxy-3-(3-propyloxymethyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methyloxyacrylic acid (B1883)

1H-NMR(DMSO-d6) 12.95(bs, 2H), 8.24(s, 2H), 7.97(dd, 1H, J=3.0 Hz, 7.65 Hz), 7.73(s, 1H), 7.37-7.40(m, 1H), 7.24(t, 1H, J=7.8 Hz), 6.72(s, 1H), 4.57(s, 2H), 3.66(s, 3H), 3.61(s, 3H), 3.47(t, 2H, J=6.3 Hz), 1.55-1.62(m, 2H), 0.91(t, 3H, J=7.2 Hz).

Example 375
Synthesis of (E)-3-(2,6-dichloro-4-{4-[2-methyloxy-3-(3-pentyloxymethyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1884)

1H NMR(DMSO-d6) 12.96(bs, 2H), 7.95-7.99(m, 3H), 7.74(s, 1H), 7.34-7.40(m, 2H), 7.24(t, 1H, J=7.8 Hz), 4.56(s, 2H), 3.65(s, 3H), 3.50(t, 2H, J=6.6 Hz),1.81 (d, 3H, J=1.8 Hz), 1.55-1.59(m, 2H), 1.30-1.34(m, 4H), 0.85-0.90(m, 3H).

Example 376
Synthesis of (E)-3-(2,6-difluoro-4-{4-[2-methyloxy-3-(3-pentyloxymethyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methyloxyacrylic acid (B1885)

1H NMR(DMSO-d6) 12.93(bs, 2H), 7.90-7.99(m, 3H), 7.74(s, 1H), 7.37-7.40(m, 1H), 7.24(t, 1H, J=7.5 Hz), 6.67(s, 1H), 4.56(s, 2H), 3.72(s, 3H), 3.65(s, 3H), 3.50(t, 2H, J=6.3 Hz), 1.55-1.60(m, 2H), 1.30-1.34(m, 4H), 0.87(t, 3H, J=6.9 Hz).

Example 377
Synthesis of (E)-3-(2,6-dichloro-4-{4-[2-methyloxy-3-(3-pentyloxymethyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1886)

1H NMR(DMSO-d6) 12.98(bs, 2H), 8.29(s, 2H), 7.96-7.99(m, 1H), 7.74(s, 1H), 7.36-7.41(m, 2H), 7.24(t, 1H, J=7.8 Hz), 4.56(s, 2H), 3.65(s, 3H), 3.50(t, 2H, J=6.3 Hz), 1.69(d, 3H, J=1.5 Hz), 1.55-1.60(m, 2H), 1.30-1.34(m, 4H), 0.87(t, 3H, J=6.9 Hz).

Example 378
Synthesis of (Z)-3-(2,6-dichloro-4-{4-[2-methyloxy-3-(3-pentyloxymethyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methyloxyacrylic acid (B1887)

1H NMR(DMSO-d6) 12.97(bs, 2H), 8.25(s, 2H), 7.97(dd, 1H, J=1.5 Hz, 7.8 Hz), 7.74(s, 1H), 7.37-7.40(m, 1H), 7.24(t, 1H, J=7.5 Hz), 6.72(s, 1H), 4.56(s, 2H), 3.65(s, 3H), 3.62(s, 3H), 3.50(t, 2H, J=6.3 Hz), 1.55-1.60(m, 2H), 1.30-1.34(m, 4H), 0.87(t, 3H, J=6.9 Hz).

Example 379
Synthesis of (E)-3-(2,6-difluoro-4-{4-[3-isopropyloxy-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1888)

1H NMR(DMSO-d6) 12.96(bs, 2H), 7.96(d, 3H, J=8.1 Hz), 7.74(s, 1H), 7.38-7.40(m, 1H), 7.34(s, 1H), 7.23(t, 1H, J=7.5 Hz), 4.56(s, 2H), 3.68-3.76(m, 1H), 3.66(s, 3H), 1.81(s, 3H), 1.19(d, 6H, J=6.3 Hz).

Example 380
Synthesis of (E)-3-(2,6-dichloro-4-{4-[3-isopropyloxy-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1889)

1H NMR(DMSO-d6) 12.98(bs, 2H), 8.29(s, 2H), 7.96(dd, 1H, J=1.5 Hz, 8.1 Hz), 7.74(s, 1H), 7.37-7.41(m, 2H), 7.23(t, 1H, J=7.8 Hz), 4.56(s, 2H), 3.68-3.76(m, 1H), 3.66(s, 3H), 1.69(d, 3H, J=1.5 Hz), 1.19(d, 6H, J=6.3 Hz).

Example 381
Synthesis of (E)-3-(4-{4-[3-(1-ethylpropyloxymethyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methylacrylic acid (B1890)

1H NMR(DMSO-d6) 13.20(bs, 2H), 7.96(d, 3H, J=8.7 Hz), 7.73(s, 1H), 7.40-7.42(m, 1H), 7.34(s, 1H), 7.24(t, 1H, J=7.5 Hz), 4.57(s, 2H), 3.65(s, 3H), 3.10-3.46(m, 1H), 1.881(d, 3H, J=1.5 Hz), 1.52-1.57(m, 4H), 0.89(t, 6H, J=7.5 Hz).

Example 382
Synthesis of (Z)-3-(4-{4-[3-(1-ethylpropyloxymethyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methyloxyacrylic acid (B1891)

1H NMR(DMSO-d6) 12.93(bs, 2H), 7.90-7.98(m, 3H), 7.73(s, 1H), 7.41(dd, 1H, J=1.8 Hz, 7.5 Hz), 7.24(t, 1H, J=7.5 Hz), 6.64(s, 1H), 4.57(s, 2H), 3.71(s, 3H), 3.66(s, 3H), 3.20-3.45(m, 1H), 1.50-1.59(m, 4H), 0.89(t, 6H, J=7.2 Hz).

Example 383
Synthesis of (E)-3-(2,6-dichloro-4-{4-[3-(1-ethylpropyloxymethyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1892)

1H NMR(DMSO-d6) 12.98(bs, 2H), 8.29(s, 2H), 7.96(dd, 1H, J=1.5 Hz, 7.8 Hz), 7.73(s, 1H), 7.40-7.42(m, 2H), 7.24(t, 1H, J=7.5 Hz), 4.57(s, 2H), 3.66(s, 3H), 3.26-3.38(m, 1H), 1.69(s, 3H), 1.50-1.59(m, 4H), 0.89(t, 6H, J=7.5 Hz).

Example 384
Synthesis of (Z)-3-(2,6-dichloro-4-{4-[3-(1-ethylpropyloxymethyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methyloxyacrylic acid (B1893)

1H NMR(DMSO-d6) 12.95(bs, 2H), 8.24(s, 2H), 7.96(dd, 1H, J=1.8 Hz, 7.8 Hz), 7.73(s, 1H), 7.41(dd, 1H, J=1.5 Hz, 7.5 Hz), 7.24(t, 1H, J=7.5 Hz), 6.71(s, 1H), 4.57(s, 2H), 3.66(s, 3H), 3.62(s, 3H), 3.24-3.38(m, 1H), 1.50-1.59(m, 4H), 0.89(t, 6H, J=7.5 Hz).

Example 385
Synthesis of (E)-3-{4-[4-(3-cyclohexyloxymethyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methylacrylic acid (B1894)

1H NMR(DMSO-d6) 12.97(bs, 2H), 7.96(d, 3H, J=8.4 Hz), 7.74(s, 1H), 7.39-7.7.41(m, 1H), 7.34(s, 1H), 7.23(t, 1H, J=7.8 Hz), 4.59(s, 2H), 3.66(s, 3H), 3.40-3.44(m, 1H), 1.91-1.94(m, 2H), 1.81(d, 3H, J=1.8 Hz), 1.69-1.71(m, 2H), 1.49-1.51(m, 1H), 1.25-1.35(m, 5H).

Example 386
Synthesis of (Z)-3-{4-[4-(3-cyclohexyloxymethyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methyloxyacrylic acid (B1895)

1H NMR(DMSO-d6) 12.94(bs, 2H), 7.90-7.98(m, 3H), 7.74(s, 1H), 7.40(d, 1H, J=7.2 Hz), 7.23(t, 1H, J=7.8 Hz), 6.65(s, 1H), 4.59(s, 2H), 3.72(s, 3H), 3.66(s, 3H), 3.33-3.43(m, 1H), 1.91-1.96(m, 2H), 1.69-1.71(m, 2H), 1.49-1.51(m, 1H), 1.23-1.35(m, 5H).

Example 387
Synthesis of (E)-3-{2,6-dichloro-4-[4-(3-cyclohexyloxymethyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1896)

1H NMR(DMSO-d6) 13.00(bs, 2H), 8.29(s, 2H), 7.97(d, 1H, J=7.5 Hz), 7.73(s, 1H), 7.38-7.40(m, 2H), 7.23(t, 1H, J=7.5 Hz), 4.59(s, 2H), 3.66(s, 3H), 3.34-3.42(m, 1H), 1.91-1.96(m, 2H), 1.69-1.74(m, 5H), 1.48-1.51(m, 1H), 1.25-1.35(m, 5H).

Example 388
Synthesis of (Z)-3-{2,6-dichloro-4-[4-(3-cyclohexyloxymethyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methyloxyacrylic acid (B1897)

1H NMR(DMSO-d6) 12.98(bs, 2H), 8.24(s, 2H), 7.96(d, 1H, J=7.8 Hz), 7.73(s, 1H), 7.39(d, 1H, J=7.2 Hz), 7.23(t, 1H, J=7.5 Hz), 6.71(s, 1H), 4.59(s, 2H), 3.66(s, 3H), 3.61(s, 3H), 3.20-3.45(m, 1H), 1.91-1.94(m, 2H), 1.69-1.70(m, 2H), 1.48-1.51(m, 1H), 1.25-1.32(m, 5H).

Example 389
Synthesis of (E)-3-[4-(4-{3-[3-(2,2-dimethylpropyloxy)propyl]phenyl}-5-methyloxythiazol-2-ylcarbamoyl)-2,6-difluorophenyl]-2-methylacrylic acid (B1898)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 7.93(s, 1H), 7.90(s, 1H), 7.77(s, 1H), 7.76(d, 1H, J=7.5 Hz), 7.34(s, 1H), 7.33(t, 1H, J=7.6 Hz), 7.11(t, 1H, J=7.6 Hz), 4.03(s, 3H), 3.37(t,2H, J=7.0 Hz), 3.03(s, 2H), 2.70(t, 2H, J=7.0 Hz), 1.80(s, 3H), 1.70-1.80(m, 2H,), 0.90(s, 9H).

Example 390
Synthesis of (E)-3-[2,6-dichloro-4-(4-{3-[3-(2,2-dimethylpropyloxy)propyl]phenyl}-5-methyloxythiazol-2-ylcarbamoyl)phenyl]-2-methylacrylic acid (B1899)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 8.20(s, 2H), 7.77(s, 1H), 7.76(d, 1H, J=7.5 Hz), 7.39(s, 1H), 7.33(t, 1H, J=7.6 Hz), 7.11(t, 1H, J=7.6 Hz), 4.05(s, 3H), 3.39(t, 2H, J=7.0 Hz), 3.03(s, 2H), 2.70(t, 2H, J=7.0 Hz), 1.70-1.80(m, 2H), 1.68(s, 3H), 0.90(s, 9H).

Example 391
Synthesis of (Z)-3-[4-(4-{3-[3-(2,2-dimethylpropyloxy)propyl]phenyl}-5-methyloxythiazol-2-ylcarbamoyl)-2,6-difluorophenyl]-2-methyloxyacrylic acid (B1900)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 7.88(s, 1H), 7.85(s, 1H), 7.80(s, 1H), 7.76(d, 1H, J=7.5 Hz), 7.33(t, 1H, J=7.6 Hz), 7.11(t, 1H, J=7.6 Hz), 6.63(s, 1H), 4.05(s, 3H), 3.71(s, 3H), 3.39(t, 2H, J=7.0 Hz), 3.03(s, 2H), 2.70(t, 2H, J=7.0 Hz), 1.70-1.80(m, 2H), 0.90(s, 9H).

Example 392
Synthesis of (Z)-3-[2,6-dichloro-4-(4-{3-[3-(2,2-dimethylpropyloxy)propyl]phenyl}-5-methyloxythiazol-2-ylcarbamoyl)phenyl]-2-methyloxyacrylic acid (B1901)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 8.20(s, 2H), 7.77(s, 1H), 7.76(d, 1H, J=7.5 Hz), 7.33(t, 1H, J=7.6 Hz), 7.11(t, 1H, J=7.6 Hz), 6.63(s, 1H), 4.05(s, 3H), 3.61(s, 3H), 3.39(t, 2H, J=7.0 Hz), 3.03(s, 2H), 2.70(t, 2H, J=7.0 Hz), 1.70-1.80(m, 2H,), 0.90(s, 9H).

Example 393
Synthesis of (E)-3-[4-(4-{3-[3-(2,2-dimethylpropyloxy)propyl]-2-fluorophenyl}-5-methyloxythiazol-2-ylcarbamoyl)-2,6-difluorophenyl]-2-methylacrylic acid (B1902)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 7.93(s, 1H), 7.90(s, 1H), 7.38(t, 1H, J=7.5 Hz), 7.35(s, 1H), 7.32(t, 1H, J=7.6 Hz), 7.11(t, 1H, J=7.6 Hz), 3.95(s, 3H), 3.37(t, 2H, J=7.0 Hz), 3.03(s, 2H), 2.70(t, 2H, J=7.0 Hz), 1.76-1.85(m, 2H), 1.80(s, 3H), 0.9(s, 9H).

Example 394
Synthesis of (E)-3-[2,6-dichloro-4-(4-{3-[3-(2,2-dimethylpropyloxy)propyl]-2-fluorophenyl}-5-methyloxythiazol-2-ylcarbamoyl)phenyl]-2-methylacrylic acid (B1903)

1H-NMR(DMSO-d6) 12.82(bs, 1H), 8.28(s, 2H), 7.40(t, 1H, J=7.6 Hz), 7.39(s, 1H), 7.25(t, 1H, J=7.6 Hz), 7.16(t, 1H, J=7.6 Hz), 3.94(s, 3H), 3.39(t, 2H, J=7.0 Hz), 3.03(s, 2H), 2.70(t, 2H, J=7.0 Hz), 1.70-1.80(m, 2H), 1.67(s, 3H), 0.90(s, 9H).

Example 395
Synthesis of (Z)-3-[4-(4-{3-[3-(2,2-dimethylpropyloxy)propyl]-2-fluorophenyl}-5-methyloxythiazol-2-ylcarbamoyl)-2,6-difluorophenyl]-2-methyloxyacrylic acid (B1904)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 7.90(s, 1H), 7.88(s, 1H), 7.38(t, 1H, J=7.5 Hz), 7.29(t, 1H, J=7.5 Hz), 7.18(t, 1H, J=7.5 Hz), 6.65(s, 1H), 3.95(s, 3H), 3.71(s, 3H), 3.39(t, 2H, J=7.0 Hz), 3.03(s, 2H), 2.70(t, 2H, J=7.0 Hz), 1.70-1.80(m, 2H), 0.90(s, 9H).

Example 396
Synthesis of (Z)-3-[2,6-difluoro-4-(4-{3[3-(2,2-dimethylpropyloxy)propyl]-2-fluorophenyl}-5-methyloxythiazol-2-ylcarbamoyl)phenyl]-2-methyloxyacrylic acid (B1905)

1H-NMR(DMSO-d6) 12.82(bs, 1H), 8.20(s, 2H), 7.40(t, 1H, J=7.6 Hz), 7.29(t, 1H, J=7.6 Hz), 7.16(t, 1H, J=7.6 Hz), 6.65(s, 1H), 3.95(s, 3H), 3.61(s, 3H), 3.39(t, 2H, J=7.0 Hz), 3.03(s, 2H), 2.70(t, 2H, J=7.0 Hz), 1.70-1.80(m, 2H), 0.90(s, 9H).

Example 397
Synthesis of (E)-3-(2,6-difluoro-4-{4-[2-fluoro-3-(1-methyloxy-2,2-dimethylpropyl)phenyl]-5-methyloxythiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1906)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 7.93(s, 1H), 7.90(s, 1H), 7.50(t, 1H, J=7.5 Hz), 7.28-7.38(m, 3H), 4.27(s, 1H), 3.95(s, 3H), 3.17(s, 3H), 1.79(s, 3H), 0.90(s, 9H).

Example 398
Synthesis of (E)-3-(2,6-dichloro-4-{4-[2-fluoro-3-(1-methyloxy-2,2-dimethylpropyl)phenyl]-5-methyloxythiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1907)

1H-NMR(DMSO-d6) 12.82(bs, 1H), 8.28(s, 2H), 746-7.52(m, 1H), 7.38(s, 1H), 7.34-7.38(m, 2H), 4.27(s, 1H), 3.95(s, 3H), 3.17(s, 3H), 1.69(s, 3H), 0.90(s, 9H).

Example 399
Synthesis of (Z)-3-(2,6-difluoro-4-{4-[2-fluoro-3-(1-methyloxy-2,2-dimethylpropyl)phenyl]-5-methyloxythiazol-2-ylcarbamoyl}phenyl)-2-methyloxyacrylic acid (B1908)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 7.90(s, 1H), 7.88(s, 1H), 7.50(m, 1H), 7.28-7.38(m, 2H), 6.65(s, 1H), 4.27(s, 1H), 3.95(s, 3H), 3.70(s, 3H), 3.17(s, 3H), 0.90(s, 9H).

Example 400
Synthesis of (Z)-3-(2,6-dichloro-4-{4-[2-fluoro-3-(1-methyloxy-2,2-dimethylpropyl)phenyl]-5-methyloxythiazol-2-ylcarbamoyl}phenyl)-2-methyloxyacrylic acid (B1909)

1H-NMR(DMSO-d6) 12.82(bs, 1H), 8.28(s, 2H), 746-7.52(m, 1H), 7.34-7.38(m, 2H), 6.65(s, 1H), 4.27(s, 1H), 3.95(s, 3H), 3.70(s, 3H), 3.17(s, 3H), 1.69(s, 3H), 0.90(s, 9H).

Example 401
Synthesis of (Z)-3-(2,6-dichloro-4-{4-[3-(3-ethyloxy-1-methyloxypropyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methyloxyacrylic acid (B1910)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 8.25(s, 2H), 8.03(t, 1H, J=7.2 Hz), 7.66(d, 1H, J=2.4 Hz), 7.32-7.40(m, 2H), 6.72(s, 1H), 4.68-4.72(m, 1H), 3.61(s, 3H), 3.45-3.54(m, 1H), 3.18(s, 3H), 1.85-2.01(m, 2H), 1.09(t, 3H, J=6.9 Hz).

Example 402
Synthesis of (Z)-3-{2,6-difluoro-4-[4-(2-fluoro-3-heptyloxymethylphenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methyloxyacrylic acid (B1911)

1H-NMR(DMSO-d6) 13.00(bs, 1H), 8.05(t, 1H, J=7.5 Hz), 7.88-7.98(m, 2H), 7.65(d, 1H, J=2.4 Hz), 7.42(t, 1H, J=6.9 Hz), 7.32(t, 1H, J=7.5 Hz), 6.66(s, 1H), 4.58(s, 2H), 3.72(s, 3H), 3.48(t, 2H, J=6.6 Hz), 1.51-1.60(m, 2H), 1.20-1.40(m, 8H), 0.85(t, 3H, J=6.6 Hz).

Example 403
Synthesis of (Z)-3-{2,6-dichloro-4-[4-(2-fluoro-3-heptyloxymethylphenyl)thiazol-2-ylcarbamoyl]phenyl-2-methyloxyacrylic acid (B1912)

1H-NMR(DMSO-d6) 13.01(bs, 1H), 8.25(s, 2H), 8.04(dt, 1H, J=1.8, 7.2 Hz), 7.65(d, 1H, J=2.4 Hz), 7.42(t, 1H, J=6.6 Hz), 7.31(t, 1H, J=7.5 Hz), 6.73(s, 1H), 4.58(s, 2H), 3.61(s, 3H), 3.48(t, 2H, J=6.6 Hz), 1.50-1.58(m, 2H), 1.20-1.40(m, 8H), 0.85(t, 3H, J=6.9 Hz).

Example 404
Synthesis of (Z)-3-{4-[4-(3-ethyloxymethyl-2-fluorophenyl)thiazol-2-ylcarbamoyl]-2,6-difluorophenyl}-2-methyloxyacrylic acid (B1913)

1H-NMR(DMSO-d6) 13.01(bs, 1H), 8.05(t, 1H, J=7.5 Hz), 7.88-7.96(m, 2H), 7.67(d, 1H, J=2.4 Hz), 7.44(t, 1H, J=6.9 Hz), 7.32(t, 1H, J=7.5 Hz), 6.66(s, 1H), 4.59(s, 2H), 3.72(s, 3H), 3.52-3.59(m, 2H), 1.18(t, 3H, J=6.9 Hz).

Example 405
Synthesis of (Z)-3-{2,6-dichloro-4-[4-(3-ethyloxymethyl-2-fluorophenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methyloxyacrylic acid (B1914)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 8.25(s, 2H), 8.04(dt, 1H, J=2.1, 6.9 Hz), 7.66(d, 1H, J=2.7 Hz), 7.43(t, 1H, J=6.3 Hz), 7.31(t, 1H, J=7.8 Hz), 6.73(s, 1H), 4.59(s, 2H), 3.61(s, 3H), 3.52-3.59(m, 2H), 1.18(t, 3H, J=6.9 Hz).

Example 406
Synthesis of (E)-3-[2,6-difluoro-4-(4-{2-fluoro-3-[1-methyloxy-3-(4-methylpentyloxy)propyl]phenyl}thiazol-2-ylcarbamoyl)phenyl]-2-methylacrylic acid (B1915)

1H-NMR(DMSO-d6) 13.01(bs, 2H), 8.07-7.30(m, 3H), 7.66(d, 1H, J=2.7 Hz), 7.32-7.42(m, 3H), 4.69-4.73(m, 1H), 3.45-3.58(m, 1H), 3.18(s, 3H), 1.84-2.40(m, 2H), 1.81(s, 3H), 1.42-1.54(m, 3H), 1.12-1.20(m, 2H), 0.84(d, 6H, J=6.6 Hz).

Example 407
Synthesis of (E)-3-(4-{4-[3-(2-cyclohexylethyloxy)-2-methylphenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methylacrylic acid (B1916)

1H-NMR(DMSO-d6) 12.97 (bs, 2H), 7.90-7.93 (m, 2H), 7.74 (s, 1H), 7.63-7.66 (m, 1H), 7.04-7.16 (m, 2H), 6.69 (s, 1H), 4.07 (t, 2H, J=6.7 Hz), 3.79 (s, 3H), 3.71(s, 3H), 0.94-1.80 (m, 16H).

Example 408
Synthesis of (Z)-3-(4-{4-[3-(2-cyclohexylethyloxy)-2-methylphenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methyloxy acrylic acid (B1917)

1H-NMR(DMSO-d6) 12.97 (bs, 2H), 7.90-7.93 (m, 2H), 7.74 (s, 1H), 7.31 (s, 1H), 7.63-7.66 (m, 1H), 7.04-7.16 (m, 2H), 4.07 (t, 2H, J=6.7 Hz), 3.79 (s, 3H), 0.94-1.80 (m, 13H).

Example 409
Synthesis of (E)-3-(2,6-dichloro-4-{4-[3-(2-cyclohexylethyloxy)-2-methylphenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1918)

1H-NMR(DMSO-d6) 12.97 (bs, 2H), 8.29 (s, 2H), 7.75 (s, 1H), 7.63-7.66 (m, 1H), 7.41 (s, 1H), 7.04-7.16 (m, 2H), 4.07 (t, 2H, J=6.4 Hz), 3.79 (s, 3H), 3.61(s, 3H), 0.94-1.80 (m, 16H).

Example 410
Synthesis of (Z)-3-(2,6-dichloro-4-{4-[3-(2-cyclohexylethyloxy)-2-methylphenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methyloxyacrylic acid (B1919)

1H-NMR(DMSO-d6) 12.97 (bs, 2H), 8.25 (s, 2H), 7.74 (s, 1H), 7.63-7.66 (m, 1H), 7.04-7.16 (m, 2H), 6.74 (s, 1H), 4.07 (t, 2H, J=6.4 Hz), 3.79 (s, 3H), 3.61(s, 3H), 0.94-1.80 (m, 13H).

Example 411
Synthesis of (E)-3-[2,6-difluoro-4-(4-{2-methyloxy-3-[2-(4-methylpentyloxy)ethyl]phenyl}thiazol-2-ylcarbamoyl)phenyl)-2-methylacrylic acid (B1920)

1H-NMR(DMSO-d6) 12.97 (bs, 2H), 7.94-7.97 (m, 2H), 7.85-7.88 (m, 1H), 7.72 (s, 1H), 7.34 (s, 1H), 7.26-7.29 (m, 1H), 7.13-7.18 (m, 1H), 3.59-3.65 (m, 5H), 3.37-3.41 (m, 2H), 2.91 (t, 2H, J=7.0 Hz), 1.81 (s, 3H), 1.44-1.53 (m, 3H), 1.12-1.20 (m, 2H), 0.84 (d, 6H, J=6.7 Hz).

Example 412
Synthesis of (Z)-3-[2,6-difluoro-4-(4-{2-methyloxy-3-[2-(4-methylpentyloxy)ethyl]phenyl}thiazol-2-ylcarbamoyl)phenyl)-2-methyloxyacrylic acid (B1921)

1H-NMR(DMSO-d6) 13.57 (bs, 1H), 12.97 (bs, 1H), 7.85-7.92 (m, 3H), 7.72 (s, 1H), 7.26-7.29 (m, 1H), 7.13-7.18 (m, 1H), 6.66 (s, 1H), 3.71 (s, 3H), 3.59-3.65 (m, 2H), 3.37-3.41 (m, 2H), 2.91 (t, 2H, J=7.0 Hz), 1.44-1.53 (m, 3H), 1.12-1.20 (m, 2H), 0.84 (d, 6H, J=6.7 Hz).

Example 413
Synthesis of (E)-3-[2,6-dichloro-4-(4-{2-methyloxy-3-[2-(4-methylpentyloxy)ethyl]phenyl}thiazol-2-ylcarbamoyl)phenyl)-2-methylacrylic acid (B1922)

1H-NMR(DMSO-d6) 12.97 (bs, 2H), 8.29 (s, 2H), 7.86-7.88 (m, 1H), 7.72 (s, 1H), 7.40 (s, 1H), 7.27-7.29 (m, 1H), 7.13-7.18 (m, 1H), 3.60-3.64 (m, 5H), 3.36-3.41 (m, 2H), 2.91 (t, 2H, J=7.0 Hz), 1.69 (s, 3H), 1.44-1.53 (m, 3H), 1.12-1.20 (m, 2H), 0.84 (d, 6H, J=6.7 Hz).

Example 414
Synthesis of (Z)-3-[2,6-dichloro-4-(4-{2-methyloxy-3-[2-(4-methylpentyloxy)ethyl]phenyl}thiazol-2-ylcarbamoyl)phenyl)-2-methyloxyacrylic acid (B1923)

1H-NMR(DMSO-d6) 13.57 (bs, 1H), 12.97 (bs, 1H), 8.25 (s, 2H), 7.85-7.88 (m, 1H), 7.72 (s, 1H), 7.26-7.29 (m, 1H), 7.13-7.18 (m, 1H), 6.74 (s, 1H), 3.59-3.65 (m, 8H), 3.37-3.41 (m, 2H), 2.91 (t, 2H, J=7.0 Hz), 1.46-1.51 (m, 3H), 1.12-1.19 (m, 2H), 0.83 (d, 6H, J=6.6 Hz).

Example 415
Synthesis of (E)-3-(2,6-difluoro-4-{4-[2-methyloxy-3-(2-pentyloxyethyl)phenyl]thiazol-2-ylcarbamoyl)phenyl)-2-methylacrylic acid (B1924)

1H-NMR(DMSO-d6) 12.96 (bs, 2H), 7.95-7.98 (m, 2H), 7.85-7.88 (m, 1H), 7.72 (s1H), 7.34 (s, 1H), 7.27-7.29 (m, 1H), 7.14-7.19 (m, 1H), 3.59-3.65 (m, 5H), 3.36-3.41 (m, 2H), 2.91 (t, 2H, J=7.4 Hz), 1.81 (s, 3H), 1.44-1.49 (m, 2H), 1.24-1.27 (m, 4H), 0.82-0.87 (m, 3H).

Example 416
Synthesis of (E)-3-(2,6-dichloro-4-{4-[2-methyloxy-3-(2-pentyloxyethyl)phenyl]thiazol-2-ylcarbamoyl)phenyl)-2-methylacrylic acid (B1925)

1H-NMR(DMSO-d6) 12.95 (bs, 2H), 8.29 (s, 2H), 7.85-7.88 (m, 1H), 7.72 (s1H), 7.41 (s, 1H), 7.27-7.29 (m, 1H), 7.13-7.19 (m, 1H), 3.59-3.65 (m, 5H), 3.36-3.41 (m, 2H), 2.91 (t, 2H, J=7.4 Hz), 1.69 (s, 3H), 1.44-1.49 (m, 2H), 1.24-1.27 (m, 4H), 0.82-0.87 (m, 3H).

Example 417
Synthesis of (E)-3-(2,6-difluoro-4-{4-[3-(2-hexyloxyethyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl)phenyl)-2-methylacrylic acid (B1926)

1H-NMR(DMSO-d6) 12.98 (bs, 2H), 7.95-7.98 (m, 2H), 7.85-7.89 (m, 1H), 7.72 (s, 1H), 7.40 (s, 1H), 7.26-7.29 (m, 1H), 7.13-7.19 (m, 1H), 3.59-3.64 (m, 5H), 3.37-3.41 (m, 2H), 2.91 (t, 2H, J=7.0 Hz), 1.81 (s, 3H), 1.44-1.49 (m, 2H), 1.24-1.27 (m, 6H), 0.82-0.87 (m, 3H).

Example 418
Synthesis of (Z)-3-(2,6-difluoro-4-{4-[3-(2-hexyloxyethyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl)phenyl)-2-methyloxyacrylic acid (B1927)

1H-NMR(DMSO-d6) 13.55 (bs, 1H), 12.98 (bs, 1H), 7.85-7.92 (m, 3H), 7.72 (s, 1H), 7.26-7.29 (m, 1H), 7.13-7.19 (m, 1H), 6.66 (s, 1H), 3.71 (s, 3H), 3.59-3.64 (m, 5H), 3.37-3.41 (m, 2H), 2.91 (t, 2H, J=7.0 Hz), 1.44-1.49 (m, 2H), 1.24-1.27 (m, 6H), 0.82-0.87 (m, 3H).

Example 419
Synthesis of (E)-3-(2,6-dichloro-4-{4-[3-(2-hexyloxyethyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl)phenyl)-2-methylacrylic acid (B1928)

1H-NMR(DMSO-d6) 12.98 (bs, 2H), 8.29 (s, 2H), 7.85-7.88 (m, 1H), 7.72 (s, 1H), 7.41 (s, 1H), 7.26-7.29 (m, 1H), 7.13-7.19 (m, 1H), 3.59-3.65 (m, 5H), 3.37-3.41 (m, 2H), 2.91 (t, 2H, J=7.0 Hz), 1.69 (s, 3H), 1.44-1.49 (m, 2H), 1.24-1.27 (m, 6H), 0.82-0.87 (m, 3H).

Example 420
Synthesis of (Z)-3-(2,6-dichloro-4-{4-[3-(2-hexyloxyethyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl)phenyl)-2-methyloxyacrylic acid (B1929)

1H-NMR(DMSO-d6) 13.57 (bs, 1H), 12.97 (bs, 1H), 8.24 (s, 2H), 7.85-7.88 (m, 1H), 7.72 (s, 1H), 7.26-7.29 (m, 1H), 7.13-7.18 (m, 1H), 6.73 (s, 1H), 3.59-3.65 (m, 8H), 3.37-3.41 (m, 2H), 2.91 (t, 2H, J=7.4 Hz), 1.44-1.49 (m, 2H), 1.24-1.27 (m, 6H), 0.82-0.87 (m, 3H).

Example 421
Synthesis of (Z)-3-[2,6-difluoro-4-(4-{2-fluoro-3-[1-methyloxy-3-(4-methylpentyloxy)propyl]phenyl}thiazol-2-ylcarbamoyl)phenyl)-2-methyloxyacrylic acid (B1930)

1H-NMR(DMSO-d6) 12.98(bs, 1H), 8.03(dt, 1H, J=3.3, 6.6 Hz), 7.87-7.96(m, 2H), 7.65(d, 1H, J=2.1 Hz), 7.31-7.41(m, 2H), 6.64(s, 1H), 4.68-4.73(m, 1H), 3.17(s, 3H), 3.45-3.58(m, 1H), 3.18(s, 3H), 1.86-1.93(m, 2H), 1.41-1.57(m, 3H), 1.12-1.22(m, 2H), 0.84(d, 6H, J=6.6 Hz).

Example 422
Synthesis of (E)-3-[2,6-dicloro-4-(4-{2-fluoro-3-[1-methyloxy-3-(4-methylpentyloxy)propyl]phenyl}thiazol-2-ylcarbamoyl)phenyl)-2-methylacrylic acid (B1931)

1H-NMR(DMSO-d6) 13.02(bs, 2H), 8.29(s, 2H), 8.03(dt, 1H, J=2.1, 7.5 Hz), 7.65(d, 1H, J=2.7 Hz), 7.31-7.44(m, 3H), 4.68-4.73(m, 1H), 3.18(s, 3H), 1.86-2.05(m, 2H), 1.69(s, 3H), 1.41-1.56(m, 3H), 1.12-1.29(m, 2H), 0.84(d, 6H, J=6.6 Hz).

Example 423
Synthesis of (Z)-3-[2,6-dicloro-4-(4-{2-fluoro-3-[1-methyloxy-3-(4-methylpentyloxy)propyl]phenyl}thiazol-2-ylcarbamoyl)phenyl)-2-methyloxyacrylic acid (B1932)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 8.25(s, 2H), 8.03(dt, 1H, J=3.3, 6.6 Hz), 7.65(d, 1H, J=2.4 Hz), 7.31-7.40(m, 2H), 6.71(s, 1H), 4.68-4.73(m, 1H), 3.61(s, 3H), 3.45-3.54(m, 1H), 3.18(s, 3H), 1.85-2.01(m, 2H), 1.41-1.55(m, 3H), 1.12-1.20(m, 2H), 0.84(d, 6H, J=6.3 Hz).

Example 424
Synthesis of (E)-3-(4-{4-[3-(2,2-dimethylpropyloxymethyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methylacrylic acid (B1933)

1H NMR(DMSO-d6) 12.93(bs, 2H), 7.93-7.97(m, 3H), 7.72(s, 1H), 7.38(dd, 1H, J=1.5 Hz, 7.5 Hz), 7.32(s, 1H), 7.23(t, 1H, J=7.5 Hz), 4.58(s, 2H), 3.64(s, 3H), 3.18(s, 2H), 1.79(d, 3H, J=1.2 Hz), 0.91(s, 9H).

Example 425
Synthesis of (E)-3-(4-{4-[3-(3,3-dimethylbutyloxymethyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methylacrylic acid (B1934)

1H NMR(DMSO-d6) 12.98(bs, 2H), 7.96(d, 3H, J=7.8 Hz), 7.74(s, 1H), 7.34-7.39(m, 2H), 7.24(t, 1H, J=7.8 Hz), 4.56(s, 2H), 3.66(s, 3H), 3.57(t, 2H, J=7.2 Hz), 1.81(s, 3H), 1.53(t, 2H, J=7.2 Hz), 0.92(s, 9H).

Example 426
Synthesis of (Z)-3-(4-{4-[3-(3,3-dimethylbutyloxymethyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methyloxyacrylic acid (B1935)

1H NMR(DMSO-d6) 12.93(bs, 2H), 7.88-7.98(m, 3H), 7.73(s, 1H), 7.37(dd, 1H, J=1.8 Hz, 7.5 Hz), 7.23(t, 1H, J=7.5 Hz), 6.65(s, 1H), 4.56(s, 2H), 3.71(s, 3H), 3.65(s, 3H), 3.57(t, 2H, J=7.2 Hz), 1.53(t, 2H, J=7.2 Hz), 0.92(s, 9H).

Example 427
Synthesis of (Z)-3-(2,6-dichloro-4-{4-[3-(3,3-dimethylbutyloxymethyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1936)

1H NMR(DMSO-d6) 12.99(bs, 2H), 8.29(s, 2H), 7.97(d, 1H, 7.2 Hz), 7.73(s, 1H), 7.37-7.40(m, 2H), 7.23(t, 1H, J=7.2 Hz), 4.56(s, 2H), 3.65(s, 3H), 3.57(t, 2H, J=7.2 Hz), 1.69(s, 3H), 1.52(t, 2H, J=7.5 Hz), 0.92(s, 9H).

Example 428
Synthesis of (Z)-3-(2,6-dichloro-4-{4-[3-(3,3-dimethylbutyloxymethyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methyloxyacrylic acid (B1937)

1H NMR(DMSO-d6) 12.97(bs, 2H), 8.25(s, 2H), 7.97(d, 1H, J=7.8 Hz), 7.74(s, 1H), 7.38(d, 1H, J=7.2 Hz), 7.24(t, 1H, J=7.5 Hz), 6.72(s, 1H), 4.57(s, 2H), 3.66(s, 3H), 3.63(s, 3H), 3.58(t, 2H, J=7.2 Hz), 1.53(t, 2H, J=7.5 Hz), 0.92(s, 9H).

Example 429
Synthesis of (E)-3-(2,6-difluoro-4-{4-[2-methyloxy-3-(4-pentyloxymethyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1938)

1H NMR(DMSO-d6) 12.99(bs, 2H), 7.95-7.99(m, 3H), 7.74(s, 1H), 7.34-7.39(m, 2H), 7.24(t, 1H, J=7.8 Hz), 4.56(s, 2H), 3.65(s, 3H), 3.49(t, 2H, J=6.9 Hz), 1.81(s, 3H), 1.49-1.62(m, 3H),1.19-1.26(m, 2H), 0.87(d, 6H, J=6.6 Hz).

Example 430
Synthesis of (Z)-3-(2,6-difluoro-4-{4-[2-methyloxy-3-(4-pentyloxymethyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methyloxyacrylic acid (B1939)

1H NMR(DMSO-d6) 12.94(bs, 2H), 7.90-7.99(m, 3H), 7.74(s, 1H), 7.37-7.39(m, 1H), 7.24(t, 1H, J=7.8 Hz), 6.66(s, 1H), 4.56(s, 2H), 3.72(s, 3H), 3.65(s, 3H), 3.49(t, 2H, J=6.6 Hz), 1.49-1.62(m, 3H), 1.19-1.26(m, 2H), 0.87(d, 6H, J=6.6 Hz).

Example 431
Synthesis of (E)-3-(2,6-dichloro-4-{4-[2-methyloxy-3-(4-pentyloxymethyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1940)

1H NMR(DMSO-d6) 12.98(bs, 2H), 8.29(s, 2H), 7.98(d, 1H, J=7.8 Hz), 7.74(s, 1H), 7.37-7.40(m, 2H), 7.24(t, 1H, J=7.5 Hz), 4.56(s, 2H), 3.66(s, 3H), 3.49(t, 2H, J=6.6 Hz), 1.69(s, 3H), 1.49-1.62(m, 3H), 1.19-1.26(m, 2H), 0.87(d, 6H, J=6.6 Hz).

Example 432
Synthesis of (Z)-3-(2,6-dichloro-4-{4-[2-methyloxy-3-(4-pentyloxymethyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methyloxyacrylic acid (B1941)

1H NMR(DMSO-d6) 12.97(bs, 2H), 8.25(s, 2H), 7.97(dd, 1H, J=1.5 Hz, 7.8 Hz), 7.74(s, 1H),7.37-7.39(m, 1H), 7.24(t, 1H, J=7.8 Hz), 6.73(s, 1H), 4.56(s, 2H), 3.65(s, 3H), 3.63(s, 3H), 3.49(t, 2H, J=6.6 Hz), 1.49-1.62(m, 3H), 1.15-1.26(m, 2H), 0.87(d, 6H, J=6.6 Hz).

Example 433
Synthesis of (E)-3-(2,6-dichloro-4-{4-[3-(3-ethyloxypropyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1942)

1H-NMR(CDCl3-d6) 8.32(s, 2H), 7.65(d, 1H, J=1.2 Hz), 7.49(dd, 1H, J=7.8, 1.8 Hz), 7.45(s, 1H), 7.24-7.28(m, 1H), 7.16(t, 1H, J=7.8 Hz), 3.57(s, 3H), 3.46-3.53(m, 4H), 2.75-2.82(m, 2H), 1.91-2.05(m, 2H), 1.86(d, 3H, J=1.5 Hz), 1.22(t, 3H, J=6.9 Hz).

Example 434
Synthesis of (Z)-3-(2,6-dichloro-4-{4-[3-(3-ethyloxypropyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methyloxyacrylic acid (B1943)

1H-NMR(DMSO-d6) 13.0(bs, 2H), 8.24(s, 2H), 7.85(dd, 1H, J=7.8, 2.1 Hz), 7.72(s, 1H), 7.13-7.24(m, 2H), 6.73(s, 1H), 3.61(s, 6H), 3.39-3.47(m, 4H), 2.68-2.75(m, 2H), 1.78-1.90(m, 2H), 1.13(t, 3H,J=6.9 Hz).

Example 435
Synthesis of (E)-3-(4-{4-[3-(3-cyclopropylmethyloxypropyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methylacrylic acid (B1944)

1H-NMR(DMSO-d6) 13.0(bs, 2H), 7.98(s, 1H), 7.95(s, 1H), 7.86(d, 1H, J=7.8 Hz), 7.73(s, 1H), 7.34(bs, 1H), 7.13-7.26(m, 2H), 3.61(s, 3H), 3.44(t, 2H, J=6.0 Hz), 3.23(d, 1H, J=6.9 Hz), 2.72(t, 2H, J=8.4 Hz), 1.80-1.90(m, 5H), 0.94-1.10(m, 1H), 0.42-0.53(m, 2H), 0.16-0.21(m, 2H).

Example 436
Synthesis of (E)-3-(2,6-dichloro-4-{4-[3-(3-cyclopropylmethyloxypropyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1945)

1H-NMR(DMSO-d6) 13.0(bs, 2H), 8.29(s, 2H), 7.86(d, 1H, J=7.8 Hz), 7.72(bs, 1H), 7.41(s, 1H), 7.13-7.26(m, 2H), 3.62(s, 3H), 3.44(t, 2H, J=6.3 Hz), 3.23(d, 2H, J=6.9 Hz), 2.72(t, 2H,J=8.4 Hz), 1.80-1.93(m, 2H), 1.69(s, 3H), 0.96-1.08(m, 1H), 0.45-0.54(m, 2H), 0.16-0.25(m, 2H).

Example 437
Synthesis of (Z)-3-(4-{4-[3-(3-cyclopropylmethyloxypropyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methyloxyacrylic acid (B1946)

1H-NMR(DMSO-d6) 13.6(bs, 1H), 13.0(bs, 1H), 7.83-7.96(m, 3H), 7.72(s, 1H), 7.13-7.26(m, 2H), 6.66(s, 1H), 3.71(s, 3H), 3.61(s, 3H), 3.44(t, 2H, J=6.3 Hz), 3.23(d, 2H, J=6.9 Hz), 2.72(t, 2H, J=8.7 Hz), 1.79-1.89(m, 2H), 0.97-1.06(m, 1H), 0.43-0.50(m, 2H), 0.14-0.21(m, 2H).

Example 438
Synthesis of (Z)-3-(2,6-dichloro-4-{4-[3-(3-cyclopropylmethyloxypropyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methyloxyacrylic acid (B1947)

1H-NMR(DMSO-d6) 13.0(bs, 2H), 8.25(s, 2H), 8.36(d, 1H, J=8.4 Hz), 7.73(s, 1H), 7.13-7.26(m, 2H), 6.73(s, 1H), 3.61(s, 6H), 3.44(t, 2H, J=5.7 Hz), 3.23(d, 2H, J=6.6 Hz), 2.69-2.76(m, 2H), 1.78-1.88(m, 2H), 0.97-1.15(m, 1H), 0.44-0.51(m, 2H), 0.16-0.20(m, 2H).

Example 439
Synthesis of (E)-3-(4-{4-[3-(3-cyclopentylmethyloxypropyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methylacrylic acid (B1948)

1H-NMR(DMSO-d6) 13.0(bs, 2H), 7.98(s, 1H), 7.95(s, 1H), 7.85(dd, 1H, J=7.5, 1.8 Hz), 7.73(s, 1H), 7.34(bs, 1H), 7.13-7.25(m, 2H), 3.61(s, 3H), 3.43(t, 2H, J=6 Hz), 3.25(d, 2H, J=6.9 Hz), 2.72(t, 2H, J=9.0 Hz), 2.06-2.16(m, 1H), 2.48-2.54(m, 5H), 1.46-1.76(m, 6H), 1.16-1.30(m, 2H).

Example 440
Synthesis of (E)-3-(2,6-dichloro-4-{4-[3-(3-cyclopentylmethyloxypropyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1949)

1H-NMR(DMSO-d6) 13.0(bs, 2H), 8.29(s, 2H), 7.86(d, 1H, J=7.2 Hz), 7.72(s, 1H), 7.40(s, 1H), 7.13-7.25(m, 2H), 3.61(s, 3H), 3.43(t, 2H, J=6.3 Hz), 3.25(d, 2H, J=6.9 Hz), 2.69-2.78(m, 2H), 2.06-2.16(m, 1H), 1.80-1.90(m, 2H), 1.64-1.76(m, 5H), 1.46-1.60(m, 4H), 1.08-1.12(m, 2H).

Example 441
Synthesis of (Z)-3-(4-{4-[3-(3-cyclopentylmethyloxypropyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methyloxyacrylic acid (B1950)

1H-NMR(DMSO-d6) 13.6(bs, 1H), 13.0(bs, 1H), 7.83-7.96(m, 3H), 7.72(s, 1H), 7.13-7.26(m, 2H), 6.66(s, 1H), 3.71(s, 3H), 3.61(s, 3H), 3.43(t, 2H, J=6.0 Hz), 3.25(d, 2H, J=6.9 Hz), 2.72(t, 2H, J=6.3 Hz), 2.06-2.16(m, 1H), 1.78-1.90(m, 2H), 1.62-1.75(m, 2H), 1.44-1.60(m, 4H), 1.18-1.21(m, 2H).

Example 442
Synthesis of (Z)-3-(2,6-dichloro-4-{4-[3-(3-cyclopentylmethyloxypropyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methyloxyacrylic acid (B1951)

1H-NMR(DMSO-d6) 13.0(bs, 2H), 8.24(s, 2H), 7.86(d, 1H, J=7.5 Hz), 7.72(s, 1H), 7.13-7.25(m, 2H), 6.73(s, 1H), 3.43(t, 2H, J=6.3 Hz), 3.25(d, 2H, J=6.9 Hz), 2.72(t, 2H, J=8.4 Hz), 2.06-2.17(m, 1H), 1.80-1.90(m, 2H), 1.62-1.76(m, 2H), 1.46-1.60(m, 4H), 1.17-1.30(m, 2H).

Example 443
Synthesis of (E)-3-(2,6-difluoro-4-{4-[3-(2-heptyloxyethyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1952)

1H-NMR(DMSO-d6) 12.96 (bs, 2H), 7.95-7.99 (m, 2H), 7.85-7.88 (m, 1H), 7.72 (s, 1H), 7.34 (s, 1H), 7.26-7.29 (m, 1H), 7.13-7.18 (m, 1H), 3.59-3.65 (m, 5H), 3.40 (t, 2H, J=6.6 Hz), 2.91 (t, 2H, J=6.9 Hz), 1.81 (d, 3H, J=1.5 Hz), 1.48 (t, 2H, J=6.6 Hz), 1.24 (bs, 8H), 0.82-0.88 (m, 3H).

Example 444
Synthesis of (Z)-3-(2,6-difluoro-4-{4-[3-(2-heptyloxyethyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methyloxyacrylic acid (B1953)

1H-NMR(DMSO-d6) 12.92 (bs, 2H), 7.85-7.92 (m, 3H), 7.72 (s, 1H), 7.26-7.29 (m, 1H), 7.13-7.18 (m, 1H), 6.66 (s, 1H), 3.71 (s, 3H), 3.59-3.64 (m, 5H), 3.40 (t, 2H, J=6.6 Hz), 2.91 (t, 2H, J=6.9 Hz), 1.46-1.51 (m, 2H), 1.24 (bs, 8H), 0.82-0.87 (m, 3H).

Example 445
Synthesis of (E)-3-[2,6-difluoro-4-(4-{2-methyloxy-3-[2-(3-methylbutyloxyethyl)phenyl}thiazol-2-ylcarbamoyl)phenyl]-2-methylacrylic acid (B1954)

1H-NMR(DMSO-d6) 12.95 (bs, 2H), 7.95-7.97 (m, 2H), 7.85-7.88(m, 1H), 7.72 (s,1H), 7.34(s, 1H), 7.26-7.29 (m, 1H), 7.13-7.19 (m, 1H), 3.59-3.65 (m, 5H), 3.43 (t, 2H, J=6.6 Hz), 2.91 (t, 2H, J=6.9 Hz), 1.81 (s, 3H), 1.58-1651 (m, 1H), 1.36-1.42 (m, 2H), 0.85 (d, 6H, J=6.6 Hz).

Example 446
Synthesis of (E)-3-[2,6-dichloro-4-(4-{2-methyloxy-3-[2-(3-methylbutyloxy)ethyl]pheny]}thiazol-2-ylcarbamoyl)phenyl]-2-methylacrylic acid (B1955)

1H-NMR(DMSO-d6) 12.98 (bs, 2H), 8.29 (s, 2H), 7.85-7.88 (m, 1H), 7.72 (s, 1H), 7.41 (s, 1H), 7.27-7.29 (m, 1H), 7.14-7.19 (m, 1H),3.60-3.66 (m, 5H), 3.43 (t, 2H, J=6.6 Hz), 2.91(t, 2H, J=7.0 Hz), 1.59-1.69 (m, 4H), 1.36-1.40 (m, 2H), 0.85 (d, 6H, J=6.6 Hz).

Example 447
Synthesis of (Z)-3-[2,6-difluoro-4-(4-{2-methyloxy-3-[2-(3-methylbutyloxy)ethyl]pheny]}thiazol-2-ylcarbamoyl)phenyl]-2-methyloxyacrylic acid (B1956)

1H-NMR(DMSO-d6) 12.92 (bs, 2H), 7.86-7.93 (m, 3H), 7.72 (s, 1H), 7.27-7.29 (m, 1H), 7.13-7.19(m, 1H), 6.67 (s, 1H), 3.71 (s, 3H), 3.62-3.64 (m, 5H), 3.43 (t, 2H, J=6.9 Hz), 2.91(t, 2H, J=6.6 Hz), 1.58-1.67 (m, 1H), 1.35-1.42 (m, 2H), 0.85 (d, 6H, J=6.4 Hz).

Example 448
Synthesis of (E)-3-(4-{4-[3-(2-cyclohexylmethyloxyethyl)-2-methyloxypheny]}thiazol-2-ylcarbamoyl)-2,6-difluorophenyl)-2-methylacrylic acid (B1957)

1H-NMR(DMSO-d6) 12.98 (bs, 2H), 7.95-7.98 (m, 2H), 7.85-7.89 (m, 1H), 7.73 (s, 1H), 7.34 (s, 1H), 7.26-7.29 (m, 1H), 7.14-7.19 (m, 1H), 3.59-3.65 (m, 5H), 3.23 (d, 2H, J=6.3 Hz), 2.91 (t, 2H, J=6.9 Hz), 1.81 (d, 3H, J=1.5 Hz), 1.63-1.68 (m, 6H), 1.08-1.21(m, 2H), 0.87-0.94 (m, 1H).

Example 449
Synthesis of (E)-3-[2,6-dichloro-4-(4-{3-[2-(2-ethylbutyloxy)ethyl]-2-methyloxyphenyl}thiazol-2-ylcarbamoyl)phenyl]-2-methylacrylic acid (B1958)

1H-NMR(DMSO-d6) 12.98 (bs, 2H), 8.29 (s, 2H), 7.85-7.89 (m, 1H), 7.72 (s, 1H), 7.41 (s, 1H), 7.27-7.30 (m, 1H), 7.14-7.19 (m, 1H), 3.60-3.66 (m, 5H), 3.30-3.32 (m, 2H), 2.91(t, 2H, J=6.9 Hz), 1.69 (s, 3H), 1.22-1.40 (m, 5H), 0.82 (t, 6H, J=7.5 Hz).

Example 450
Synthesis of (E)-3-[4-(4-{3-[2-(2-ethylbutyloxy)ethyl]-2-methyloxyphenyl}thiazol-2-ylcarbamoyl)-2,6-difluorophenyl]-2-methylacrylic acid (B1959)

1H-NMR(DMSO-d6) 12.97 (bs, 2H), 7.95-7.98 (m, 2H), 7.85-7.89 (m, 1H), 7.72 (s, 1H), 7.42 (s, 1H), 7.27-7.29 (m, 1H), 7.13-7.19 (m, 1H), 3.60-3.65 (m, 5H), 3.30-3.32 (m, 2H), 2.91(t, 2H, J=6.9 Hz), 1.81 (s, 3H), 1.22-1.40 (m, 5H), 0.82 (t, 6H,J=7.3 Hz).

Example 451
Synthesis of (Z)-3-[2,6-dicholoro-4-(4-{3-[2-(2-ethylbutyloxy)ethyl]-2-methyloxyphenyl}thiazol-2-ylcarbamoyl)phenyl]-2-methyloxyacrylic acid (B1960)

1H-NMR(DMSO-d6) 12.95 (bs, 2H), 8.24 (s, 1H), 7.85-7.88 (m, 1H), 7.72(s, 1H), 7.27-7.30 (m, 1H), 7.13-7.18(m, 1H), 6.73 (s, 1H), 3.60-3.64 (m, 8H), 3.30-3.33 (m, 2H), 2.91(t, 2H, J=6.7 Hz), 1.22-1.40 (m, 5H), 0.82 (t, 6H,J=7.3 Hz).

Example 452
Synthesis of (E)-3-[4-(4-{3-[2-(4-chlorobutyloxy)ethyl]-2-methyloxyphenyl}thiazol-2-ylcarbamoyl)-2,6-difluorophenyl]-2-methylacrylic acid (B1961)

1H-NMR(DMSO-d6) 13.01 (bs, 2H), 7.95-7.98 (m, 2H), 7.86-7.88 (m, 1H), 7.72(s, 1H), 7.26-7.41 (m, 2H), 7.14-7.19 (m, 1H), 3.61-3.65 (m, 7H), 3.44(t, 2H, J=6.3 Hz), 2.91 (t, 2H, J=6.9 Hz), 1.70-1.81 (m, 5H), 1.60-1.66 (m, 2H).

Example 453
Synthesis of (Z)-3-[4-(4-{3-[2-(4-chlorobutyloxy)ethyl]-2-methyloxyphenyl}thiazol-2-ylcarbamoyl)-2,6-difluorophenyl]-2-methyloxyacrylic acid (B 1962)

1H-NMR(DMSO-d6) 12.91 (bs, 2H), 7.85-7.92 (m, 3H), 7.72 (s, 1H), 7.26-7.29 (m, 1H), 7.13-7.19(m, 1H), 6.66 (s, 1H), 3.71 (s, 3H), 3.60-3.65 (m, 7H), 2.91(t, 2H, J=6.9 Hz), 1.72-1.77 (m, 2H), 1.59-1.63 (m, 2H).

Example 454
Synthesis of (E)-3-[2,6-dichloro-4-(4-{3-[2-(4-chlorobutyloxy)ethyl]-2-methyloxyphenyl}thiazol-2-ylcarbamoyl)phenyl]-2-methylacrylic acid (B 1963)

1H-NMR(DMSO-d6) 12.98 (bs, 2H), 8.29 (s, 2H), 7.86-7.88 (m, 1H), 7.72(s, 1H), 7.41 (s, 1H), 7.27-7.29 (m, 1H), 7.14-7.19 (m, 1H), 3.61-3.66 (m, 7H), 3.46 (t, 2H, J=6.1 Hz), 2.91 (t, 2H, J=6.7 Hz), 1.59-1.77 (m, 7H).

Example 455
Synthesis of (Z)-3-[2,6-dichloro-4-(4-{3-[2-(4-chlorobutyloxy)ethyl]-2-methyloxyphenyl}thiazol-2-ylcarbamoyl)phenyl]-2-methyloxyacrylic acid (B 1964)

1H-NMR(DMSO-d6) 12.95 (bs, 2H), 8.24 (s, 2H), 7.86-7.88 (m, 1H), 7.72 (s, 1H), 7.27-7.29 (m, 1H), 7.14-7.19 (m, 1H), 6.73 (s, 1H), 3.61-3.65 (m, 10H), 3.42-3.46 (m, 2H), 2.90-2.94 (m, 2H), 1.58-1.77 (m, 5H).

Example 456
Synthesis of (E)-3-(2,6-difluoro-4-{4-[2-fluoro-3-(3-isobutyloxy-1-methyloxypropyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B 1965)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 8.06(t, 1H, J=7.5 Hz), 7.96(s, 1H), 7.93(s, 1H), 7.64(s, 1H), 7.30-7.40(m, 3H), 4.72(t, 1H, J=6.5 Hz), 3.50-3.58(m, 1H), 3.35-3.42(m, 1H), 3.17(s, 3H), 3.09-3.16(m, 2H), 1.85-1.95(m, 2H), 1.79(s, 3H), 1.74-1.79(m, 1H), 0.85(d, 6H, J=6.0 Hz).

Example 457
Synthesis of (E)-3-(2,6-dichloro-4-{4-[2-fluoro-3-(3-isobutyloxy-1-methyloxypropyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B 1966)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 8.29(s, 2H), 8.06(t, 1H, J=7.5 Hz), 7.64(s, 1H), 7.30-7.40(m, 3H), 4.72(t, 1H, J=6.5 Hz), 3.50-3.58(m, 1H), 3.35-3.42(m, 1H), 3.17(s, 3H), 3.09-3.16(m, 2H), 1.85-1.95(m, 2H), 1.74-1.79(m, 1H), 1.68(s, 3H), 0.85(d, 6H, J=6.0 Hz).

Example 458
Synthesis of (Z)-3-(2,6-difluoro-4-{4-[2-fluoro-3-(3-isobutyloxy-1-methyloxypropyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methyloxy acrylic acid (B1967)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 8.06(t, 1H, J=7.5 Hz), 7.96(s, 1H), 7.93(s, 1H), 7.64(s, 1H), 7.30-7.40(m, 2H), 6.65(s, 1H), 4.72(t, 1H, J=6.5 Hz), 3.71(s, 3H), 3.50-3.58(m, 1H), 3.35-3.42(m, 1H), 3.17(s, 3H), 3.09-3.16(m, 2H), 1.85-1.95(m, 2H), 1.74-1.79(m, 1H), 0.85(d, 6H, J=6.0 Hz).

Example 459
Synthesis of (Z)-3-(2,6-dichloro-4-{4-[2-fluoro-3-(3-isobutyloxy-1-methyloxypropyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methyloxyacrylic acid (B 1968)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 8.25(s, 2H), 8.06(t, 1H, J=7.5 Hz), 7.64(s, 1H), 7.30-7.40(m, 2H), 6.72(s, 1H), 4.72(t, 1H, J=6.5 Hz), 3.61(s, 3H), 3.50-3.58(m, 1H), 3.35-3.42(m, 1H), 3.17(s, 3H), 3.09-3.16(m, 2H), 1.85-1.95(m, 2H), 1.74-1.79(m, 1H), 0.85 (d, 6H, J=6.0 Hz).

Example 460
Synthesis of (E)-3-(4-{4-[3-(2-ethylbutyloxymethyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methylacrylic acid (B 1969)

1H-NMR(DMSO-d6) 13.01(bs, 2H), 8.04(dt, 1H, J=1.5, 7.5 Hz), 7.92-8.00(m, 2H), 7.65(d, 1H, J=2.7 Hz), 7.43(dt, 1H, J=2.1, 7.5 Hz), 7.34(s, 1H), 7.31(t, 1H, J=7.5 Hz), 4.59(s, 2H), 1.81(s, 3H), 1.25-1.49(m, 5H), 0.84(t, 6H, J=7.5 Hz).

Example 461
Synthesis of (Z)-3-(4-{4-[3-(2-ethylbutyloxymethyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methyloxyacrylic acid (B1970)

1H-NMR(DMSO-d6) 12.98(bs, 1H), 8.04(dt, 1H, J=1.8, 7.8 Hz), 7.87-7.95(m, 2H), 7.65(d, 1H, J=2.7 Hz), 7.43(t, 1H, J=6.6 Hz), 7.31(t, 1H, J=7.5 Hz), 6.64(s, 1H), 4.59(s, 2H), 3.71(s, 3H), 3.40(d, 2H, J=5.7 Hz), 1.25-1.49(m, 5H), 0.84(t, 6H, J=7.5 Hz).

Example 462
Synthesis of (E)-3-(2,6-dichloro-4-{4-[3-(2-ethylbutyloxymethyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B1971)

1H-NMR(DMSO-d6) 13.01(bs, 2H), 8.29(s, 2H), 8.04(dt, 1H, J=1.5, 7.5 Hz), 7.64(d, 1H, J=2.4 Hz), 7.38-7.46(m, 2H), 7.31(t, 1H, J=7.5 Hz), 4.59(s, 2H), 3.40(d, 2H, J=5.7 Hz), 1.69(s, 3H), 1.25-1.49(m, 5H), 0.84(t, 6H, J=7.5 Hz).

Example 463
Synthesis of (Z)-3-(2,6-dichloro-4-{4-[3-(2-ethylbutyloxymethyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methyloxyacrylic acid (B 1972)

1H-NMR(DMSO-d6) 13.00(bs, 1H), 8.24(s, 2H), 8.04(dt, 1H, J=1.8, 7.8 Hz), 7.65(d, 1H, J=2.7 Hz), 7.43(t, 1H, J=6.6 Hz), 7.31(t, 1H, J=7.5 Hz), 6.71(s, 1H), 4.59(s, 2H), 3.61(s, 3H), 3.40(d, 2H, J=5.4 Hz), 1.25-1.49(m, 5H), 0.84(t, 6H, J=7.5 Hz).

Example 464
Synthesis of (E)-3-{2,6-difluoro-4-[4-(2-fluoro-3-isobutyloxymethylphenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methylacrylic acid (B 1973)

1H-NMR(DMSO-d6) 13.01(bs, 2H), 8.04(dt, 1H, J=1.8, 7.8 Hz), 7.92-8.00(m, 2H), 7.65(d, 1H, J=2.4 Hz), 7.43(t, 1H, J=6.0 Hz), 7.34(s, 1H), 7.32(t, 1H, J=7.5 Hz), 4.60(s, 2H), 1.80-1.93(m, 1H), 1.81(s, 3H), 0.89(d, 6H, J=6.6 Hz).

Example 465
Synthesis of (Z)-3-{2,6-difluoro-4-[4-(2-fluoro-3-isobutyloxymethylphenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methyloxyacrylic acid (B1974)

1H-NMR(DMSO-d6) 12.98(bs, 1H), 8.04(dt, 1H, J=1.8, 7.5 Hz), 7.87-7.95(m, 2H), 7.65(d, 1H, J=2.4 Hz), 7.43(dt, 1H, J=1.8, 6.6 Hz), 7.32(t, 1H, J=7.5 Hz), 6.66(s, 1H), 4.59(s, 2H), 3.71(s, 3H), 1.80-1.93(m, 1H), 0.89(d, 6H, J=6.9 Hz).

Example 466
Synthesis of (E)-3-{2,6-dichloro-4-[4-(2-fluoro-3-isobutyloxymethylphenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methylacrylic acid (B 1975)

1H-NMR(DMSO-d6) 13.01(bs, 2H), 8.29(s, 2H), 8.04(dt, 1H, J=2.1, 7.8 Hz), 7.65(d, 1H, J=2.7 Hz), 7.38-7.46(m, 2H), 7.32(t, 1H, J=7.5 Hz), 4.60(s, 2H), 1.82-1.91(m, 1H), 1.69(s, 3H), 0.89(d, 6H, J=6.6 Hz).

Example 467
Synthesis of (Z)-3-{2,6-dichloro-4-[4-(2-fluoro-3-isobutyloxymethylphenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methyloxyacrylic acid (B 1976)

1H-NMR(DMSO-d6) 13.01(bs, 1H), 8.25(s, 2H), 8.04(dt, 1H, J=1.8, 7.8 Hz), 7.66(d, 1H, J=2.4 Hz), 7.44(t, 1H, J=6.6 Hz), 7.32(t, 1H, J=7.5 Hz), 6.72(s, 1H), 4.60(s, 2H), 3.62(s, 3H), 1.82-1.89(m, 1H), 0.89(d, 6H, J=6.9 Hz).

Example 468
Synthesis of (Z)-3-(2,6-difluoro-4-{4-[2-fluoro-3-(3-methylbutyloxymethyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methyloxyacrylic acid (B 1977)

1H-NMR(DMSO-d6) 12.98(bs, 1H), 8.04(dt, 1H, J=1.5, 7.2 Hz), 7.86-7.96(m, 2H), 7.66(d, 1H, J=2.4 Hz), 7.43(d, 1H, J=6.0 Hz), 7.31(t, 1H, J=7.5 Hz), 6.65(s, 1H), 4.59(s, 2H), 3.72(s, 3H), 3.52(t, 2H, J=6.6 Hz), 1.63-1.76(m, 1H), 1.42-1.49 (m, 2H), 0.88(d, 6H, J=6.6 Hz).

Example 469
Synthesis of (Z)-3-(2,6-dichloro-4-{4-[2-fluoro-3-(3-methylbutyloxymethyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methyloxy acrylic acid (B1978)

1H-NMR(DMSO-d6) 13.00(bs, 1H), 8.25(s, 2H), 8.04(dt, 1H, J=1.5, 7.5 Hz), 7.65(d, 1H, J=2.4 Hz), 7.42(t, 1H, J=6.9 Hz), 7.31(t, 1H, J=7.2 Hz), 6.72(s, 1H), 4.58(s, 2H), 3.61(s, 3H), 3.52(t, 2H, J=6.6 Hz), 1.62-1.76(m, 1H), 1.42-1.49 (m, 2H), 0.88(d, 6H, J=6.6 Hz).

Example 470
Synthesis of (E)-3-{4-[4-(3-cyclobutylmethyloxymethyl-2-fluorophenyl)thiazol-2-ylcarbamoyl]-2,6-difluorophenyl)-2-methylacrylic acid (B 1979)

1H-NMR(DMSO-d6) 13.00(bs, 2H), 8.04(dt, 1H, J=2.1, 7.8 Hz), 7.92-8.00(m, 2H), 7.65(d, 1H, J=2.4 Hz), 7.42(dt, 1H, J=1.8, 6.9 Hz), 7.34(s, 1H), 7.31(t, 1H, J=7.8 Hz), 4.59(s, 2H), 3.48(d, 2H, J=6.6 Hz), 2.50-2.61(m, 1H), 1.64-2.04(m, 9H).

Example 471
Synthesis of (Z)-3-{4-[4-(3-cyclobutylmethyloxymethyl-2-fluorophenyl)thiazol-2-ylcarbamoyl]-2,6-difluorophenyl)-2-methyloxyacrylic acid (B1980)

1H-NMR(DMSO-d6) 12.97(bs, 1H), 8.04(dt, 1H, J=1.8, 7.8 Hz), 7.86-7.95(m, 2H), 7.65(d, 1H, J=2.4 Hz), 7.43(dt, 1H, J=1.8, 7.5 Hz), 7.31(t, 1H, J=7.5 Hz), 6.65(s, 1H), 4.60(s, 2H), 3.71(s, 3H), 3.48(d, 2H, J=6.6 Hz), 2.50-2.61(m, 1H), 1.67-2.05(m, 6H).

Example 472
Synthesis of (E) -3-{2,6-dichloro-4-[4-(3-cyclobutylmethyloxymethyl-2-fluorophenyl)thiazol-2-ylcarbamoyl]phenyl)-2-methylacrylic acid (B1981)

1H-NMR(DMSO-d6) 13.03(bs, 2H), 8.29(s, 2H), 8.04(t, 1H, J=7.2 Hz), 7.65(d, 1H, J=2.7 Hz), 7.38-7.48(m, 2H), 7.31(t, 1H, J=7.8 Hz), 4.60(s, 2H), 3.47(d, 2H, J=6.6 Hz), 1.62-2.03(m, 6H), 1.69(s, 3H).

Example 473
Synthesis of (Z)-3-{2,6-dichloro-4-[4-(3-cyclobutylmethyloxymethyl-2-fluorophenyl)thiazol-2-ylcarbamoyl]phenyl)-2-methyloxyacrylic acid (B1982)

1H-NMR(DMSO-d6) 13.00(bs, 1H), 8.24(s, 2H), 8.04(dt, 1H, J=1.8, 7.5 Hz), 7.65(d, 1H, J=2.7 Hz), 7.43(t, 1H, J=6.3 Hz), 7.31(t, 1H, J=7.5 Hz), 6.72(s, 1H), 4.60(s, 2H), 3.61(s, 3H), 3.48(d, 2H, J=6.9 Hz), 2.48-2.52(m, 1H), 2.05-1.67 (m, 6H).

Example 474
Synthesis of (E)-3-(4-{4-[3-(2,2-dimethylpropyloxymethyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methylacrylic acid (B 1983)

1H-NMR(DMSO-d6) 13.01(bs, 2H), 7.92-8.08(m, 2H), 7.65(d, 1H, J=2.4 Hz), 7.44(t, 1H, J=5.4 Hz), 7.34(d, 1H, J=2.4 Hz), 7.32 (t, 1H, J=7.5 Hz), 4.62(s, 2H), 3.18(s, 2H), 1.81(s, 3H), 0.91(s, 9H).

Example 475
Synthesis of (Z)-3-(4-{4-[3-(2,2-dimethylpropyloxymethyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methyloxyacrylic acid (B 1984)

1H-NMR(DMSO-d6) 12.98(bs, 1H), 8.04(dt, 1H, J=1.8, 7.5 Hz), 7.87-7.94(m, 2H), 7.65(d, 1H, J=2.7 Hz), 7.45(dt, 1H, J=1.8, 6.6 Hz), 7.32(t, 1H, J=7.5 Hz), 6.66(s, 1H), 4.62(s, 2H), 3.61(s, 3H), 3.18(s, 2H), 0.91(s, 9H).

Example 476
Synthesis of (E)-3-(2,6-dichloro-4-{4-[3-(2,2-dimethylpropyloxymethyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B 1985)

1H-NMR(DMSO-d6) 13.00(bs, 2H), 8.29(s, 2H), 8.04(dt, 1H, J=1.8, 7.5 Hz), 7.63(d, 1H, J=2.4 Hz), 7.44(dt, 1H, J=2.1, 8.4 Hz), 7.40 (d, 1H, J=1.2 Hz), 7.32(t, 1H, J=7.8 Hz), 4.62(s, 2H), 3.18(s, 2H), 1.39(s, 3H), 0.91(s, 9H).

Example 477
Synthesis of (Z)-3-(2,6-dichloro-4-{4-[3-(2,2-dimethyl-propyloxymethyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methyloxyacrylic acid (B 1986)

1H-NMR(DMSO-d6) 13.01(bs, 1H), 8.24(s, 2H), 8.04(dt, 1H, J=1.5, 7.2 Hz), 7.65(d, 1H, J=2.7 Hz), 7.43(t, 1H, J=6.6 Hz), 7.32(t, 1H, J=7.5 Hz), 6.72(s, 1H), 4.62(s, 2H), 3.61(s, 3H), 3.18(s, 2H), 0.91(s, 9H).

Example 478
Synthesis of (E)-3-(4-{4-[3-(2-cyclopentyethyloxymethyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methylacrylic acid (B 1987)

1H-NMR(DMSO-d6) 12.99(bs, 2H), 8.04(dt, 1H, J=1.8, 7.8 Hz), 7.92-8.02(m, 2H), 7.66(d, 1H, J=2.7 Hz), 7.39-7.46(m, 1H), 7.²8-7.36(m, 2H), 4.59(s, 2H), 3.51(t, 2H, J=6.9 Hz), 1.45-1.95(m, 11H), 1.00-1.18(m, 2H).

Example 479
Synthesis of (E)-3-(2,6-dichloro-4-{4-[3-(2-cyclopentyethyloxymethyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B 1988)

1H-NMR(DMSO-d6) 13.04(bs, 2H), 8.29(s, 2H), 8.01-8.07(m, 1H), 7.65(d, 1H, J=2.4 Hz), 7.38-7.47(m, 2H), 7.31(t, 1H, J=7.8 Hz), 4.59(s, 2H), 3.51(t, 2H, J=6.6 Hz), 1.65-1.90(m, 6H), 1.40-1.65(m, 5H), 1.00-1.17(m, 2H).

Example 480
Synthesis of (Z)-3-(2,6-dichloro-4-{4-[3-(2-cyclopentyethyloxymethyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methyloxyacrylic acid (B 1989)

1H-NMR(DMSO-d6) 12.85(bs, 1H), 8.07(s, 2H), 7.87(dt, 1H, J=1.8, 7.8 Hz), 7.48(d, 1H, J=1.8 Hz), 7.22-7.30(m, 1H), 7.14(t, 1H, J=7.8 Hz), 6.55(s, 1H), 4.41(s, 2H), 3.44(s, 3H), 3.33(t, 2H, J=6.6 Hz), 1.26-1.73(m, 9H), 0.86-1.00(m, 2H).

Example 481
Synthesis of (E)-3-{2,6-difluoro-4-[4-(3-heptyloxymethyl-2-methyloxyphenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methylacrylic acid (B 1990)

1H-NMR(DMSO-d6) 12.96 (bs, 2H), 7.95-7.98 (m, 3H), 7.74 (s, 1H), 7.34-7.39 (m, 2H), 7.21-7.26 (m, 1H), 4.56 (s, 2H), 3.65 (s, 3H), 3.50 (t, 2H, J=6.0 Hz), 1.81 (s, 3H), 1.54-1.56 (m, 2H), 1.25 (bs, 8H), 0.83-0.86 (m, 3H).

Example 482
Synthesis of (E)-3-{2,6-dichloro-4-[4-(3-heptyloxymethyl-2-methyloxyphenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methylacrylic acid (B 1991)

1H-NMR(DMSO-d6) 12.98 (bs, 2H), 8.29 (s, 2H), 7.96-7.99 (m, 1H), 7.74 (s, 1H), 7.36-7.41 (m, 2H), 7.21-7.26 (m, 1H), 4.56 (s, 2H), 3.66 (s, 3H), 3.50 (t, 2H, J=6.0Hz), 169 (s, 3H), 1.52-1.59 (m, 2H), 1.25 (bs, 8H), 0.83-0.88 (m, 3H).

Example 483
Synthesis of (E)-3-{2,6-difluoro-4-[4-(3-hexyloxymethyl-2-methyloxyphenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methylacrylic acid (B1992)

1H-NMR(DMSO-d6) 12.96 (bs, 2H), 7.95-7.99 (m, 3H), 7.74 (s, 1H), 7.34-7.39 (m, 2H), 7.21-7.26 (m, 1H), 4.56 (s, 2H), 3.65 (s, 3H), 3.50 (t, 2H, J=6.0 Hz), 1.81 (s, 3H), 1.52-1.59 (m, 2H), 1.27-1.36 (m, 6H), 0.84-0.88 (m, 3H).

Example 484
Synthesis of (E)-3-{2,6-dichloro-4-[4-(3-hexyloxymethyl-2-methyloxyphenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methylacrylic acid (B1993)

1H-NMR(DMSO-d6) 12.96 (bs, 2H), 8.29 (s, 2H), 7.96-7.98 (m, 1H), 7.73 (s, 1H), 7.36-7.40 (m, 2H), 7.21-7.26 (m, 1H), 4.56 (s, 2H), 3.65 (s, 3H), 3.50 (t, 2H, J=6.0Hz), 1.69 (s, 3H), 1.52-1.59 (m, 2H), 1.26-1.36 (m, 6H), 0.84-0.88 (m, 3H).

Example 484
Synthesis of (Z)-3-{2,6-dichloro-4-[4-(3-hexyloxymethyl-2-methyloxyphenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methyloxyacrylic acid (B 1994)

1H-NMR(DMSO-d6) 12.95 (bs, 2H), 8.25 (s, 2H), 7.96-7.99 (m, 1H), 7.73 (s, 1H), 7.36-7.39 (m, 1H), 7.21-7.27 (m, 1H), 6.73 (s, 1H), 4.56 (s, 2H), 3.65 (s, 3H), 3.62 (s, 3H), 3.50 (t, 2H, J=6.3Hz), 1.52-1.59 (m, 2H), 1.26-1.36 (m, 6H), 0.84-0.88 (m, 3H)

Example 486
Synthesis of (E)-3-{4-[4-(3-butyloxymethyl-2-methyloxyphenyl)thiazol-2-ylcarbamoyl]-2,6-dichlorophenyl}-2-methylacrylic acid (B 1995)

1H-NMR(DMSO-d6) 12.98 (bs, 2H), 8.29 (s, 2H), 7.96-7.99 (m, 1H), 7.74 (s, 1H), 7.37-7.41 (m, 2H), 7.21-7.26 (m, 1H), 4.56 (s, 2H), 3.66 (s, 3H), 3.51 (t, 2H, J=6.3 Hz), 1.69 (s, 3H), 1.51-1.60 (m, 2H), 1.30-1.43 (m, 2H), 0.87-0.92 (m, 3H).

Example 487
Synthesis of (Z)-3-{4-[4-(3-butyloxymethyl-2-methyloxyphenyl)thiazol-2-ylcarbamoyl]-2,6-dichlorophenyl}-2-methyloxyacrylic acid (B 1996)

1H-NMR(DMSO-d6) 12.96 (bs, 2H), 8.25 (s, 2H), 7.96-7.99 (m, 1H), 7.73 (s, 1H), 7.36-7.40 (m, 1H), 7.21-7.26 (m, 1H), 6.73 (s, 1H), 4.56 (s, 2H), 3.66 (s, 3H), 3.61 (s, 3H), 3.51 (t, 2H, J=6.0 Hz), 1.51-1.60 (m, 2H), 1.31-1.43 (m, 2H), 0.87-0.92 (m, 3H).

Example 488
Synthesis of (E)-3-{4-[4-(3-butyloxymethyl-2-methyloxyphenyl)thiazol-2-ylcarbamoyl]-2,6-difluorophenyl}-2-methylacrylic acid (B 1997)

1H-NMR(DMSO-d6) 12.97 (bs, 2H), 7.96-8.00 (m, 3H), 7.75 (s, 1H), 7.34-7.39 (m, 2H), 7.22-7.27 (m, 1H), 4.56 (s, 2H), 3.66 (s, 3H), 3.51 (t, 2H, J=6.0 Hz), 1.81 (s, 3H), 1.51-1.60 (m, 2H), 1.31-1.43 (m, 2H), 0.87-0.92 (m, 3H).

Example 489
Synthesis of (E)-3-{2,6-difluoro-4-[4-(3-heptyloxy-2-methyloxyphenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methylacrylic acid (B 1998)

1H-NMR(DMSO-d6) 12.95 (bs, 2H), 7.95-7.97 (m, 2H), 7.74 (s, 1H), 7.64-7.66 (m, 1H), 7.34 (s, 1H), 7.10-7.16 (m, 1H), 7.02-7.04 (m, 1H), 4.03 (t, 2H, J=6.3 Hz), 3.80 (s, 3H), 1.74-1.80 (m, 5H), 1.43-1.50 (m, 2H), 1.30-1.36 (m, 6H). 0.86-0.90 (m, 3H).

Example 490
Synthesis of (E)-3-{2,6-dichloro-4-[4-(3-heptyloxy-2-methyloxyphenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methylacrylic acid (B 1999)

1H-NMR(DMSO-d6) 12.95 (bs, 2H), 8.29 (s, 2H), 7.75 (s, 1H), 7.64-7.66 (m, 1H), 7.40 (s, 1H), 7.10-7.15 (m, 1H), 7.02-7.05 (m, 1H), 4.03 (t, 2H, J=6.0 Hz), 3.80 (s, 3H), 1.76-1.81 (m, 2H), 1.69 (s, 3H), 1.45-1.50 (m, 2H), 1.30-1.36 (m, 6H). 0.86-0.90 (m, 3H).

Example 491
Synthesis of (Z)-3-{2,6-difluoro-4-[4-(3-heptyloxy-2-methyloxyphenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methyloxyacrylic acid (B2000)

1H-NMR(DMSO-d6) 13.56 (bs, 1H), 12.87 (bs, 1H), 7.89-7.92 (m, 2H), 7.74 (s, 1H), 7.63-7.66 (m, 1H), 7.10-7.15 (m, 1H), 7.02-7.05 (m, 1H), 6.66(s, 1H), 4.03 (t, 2H, J=6.0 Hz), 3.80 (s, 3H), 3.71 (s, 3H), 1.76-1.83 (m, 3H), 1.45-1.50 (m, 2H), 1.30-1.39 (m, 6H). 0.86-0.90 (m, 3H).

Example 492
Synthesis of (Z)-3-{2,6-dichloro-4-[4-(3-heptyloxy-2-methyloxyphenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methyloxyacrylic acid (B2001)

1H-NMR(DMSO-d6) 12.90 (bs, 2H), 8.24 (s, 2H), 7.74 (s, 1H), 7.63-7.66 (m, 1H), 7.10-7.15 (m, 1H), 7.01-7.05 (m, 1H), 6.73 (s, 1H), 4.03 (t, 2H, J=6.0 Hz), 3.80 (s, 3H), 3.61 (s, 3H), 1.76-1.83 (m, 3H), 1.45-1.50 (m, 2H), 1.30-1.39 (m, 6H). 0.86-0.90 (m, 3H).

Example 493
Synthesis of (E)-3-[2,6-difluoro-4-(4-{3-[2-(4-fluorobutyloxy)ethyl]-2-methyloxyphenyl}thiazol-2-ylcarbamoyl)phenyl]-2-methylacrylic acid (B 2002)

1H-NMR(DMSO-d6) 12.96 (bs, 2H), 7.95-7.88 (m, 2H), 7.85-7.88 (m, 1H), 7.72 (s, 1H), 7.33 (s, 1H), 7.26-7.29 (m, 1H), 7.13-7.19 (m, 1H), 4.50 (t, 1H, J=6.0 Hz), 4.34 (t, 1H, J=6.0 Hz), 3.62-3.66 (m, 5H), 3.45 (t, 2H, J=6.3 Hz), 2.91 (t, 2H, J=7.0 Hz), 1.81 (s, 3H), 1.55-1.73 (m, 4H).

Example 494
Synthesis of (E)-3-[2,6-dichloro-4-(4-{3-[2-(4-fluorobutyloxy)ethyl]-2-methyloxyphenyl}thiazol-2-ylcarbamoyl)phenyl]-2-methylacrylic acid (B2003)

1H-NMR(DMSO-d6) 12.97 (bs, 2H), 8.29 (s, 2H), 7.85-7.88 (m, 1H), 7.72 (s, 1H), 7.40 (s, 1H), 7.26-7.29 (m, 1H), 7.14-7.19 (m, 1H), 4.50 (t, 1H, J=6.0 Hz), 4.34 (t, 1H, J=6.0 Hz), 3.62-3.66 (m, 5H), 3.45 (t, 2H, J=6.3 Hz), 2.91 (t, 2H, J=7.0 Hz), 1.55-1.73 (m, 7H).

Example 495
Synthesis of (E)-3-{2,6-difluoro-4-[4-(2-methyloxy-3-octyloxyphenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methylacrylic acid (B2004)

1H-NMR(DMSO-d6) 12.92 (bs, 2H), 7.95-7.97 (m, 2H), 7.75 (s, 1H), 7.64-7.66 (m, 1H), 7.34 (s, 1H), 7.10-7.15 (m, 1H), 7.02-7.04 (m, 1H), 4.03 (t, 2H, J=6.3 Hz), 3.80 (s, 3H), 1.76-1.81 (m, 5H), 1.43-1.50 (m, 2H), 1.28-1.36 (m, 8H). 0.86-0.90 (m, 3H).

Example 496
Synthesis of (E)-3-{2,6-dichloro-4-[4-(2-methyloxy-3-octyloxyphenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methylacrylic acid (B2005)

1H-NMR(DMSO-d6) 12.94 (bs, 2H), 8.28 (s, 2H), 7.74 (s, 1H), 7.63-7.66 (m, 1H), 7.40 (s, 1H), 7.10-7.15 (m, 1H), 7.01-7.04 (m, 1H), 4.03 (t, 2H, J=6.0 Hz), 3.80 (s, 3H), 1.75-1.80 (m, 2H), 1.69 (s, 3H), 1.45-1.50 (m, 2H), 1.30-1.36 (m, 8H). 0.86-0.90 (m, 3H).

Example 497
Synthesis of (E)-3-[4-(4-{3-[3-(2,2-dimethylpropyloxy)-1-methyloxypropyl]-2-fluorophenyl}thiazol-2-ylcarbamoyl)-2,6-difluorophenyl]-2-methylacrylic acid (B2006)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 8.06(t, 1H, J=7.5 Hz), 7.96(s, 1H), 7.93(s, 1H), 7.64(s, 1H), 7.30-7.40(m, 3H), 4.72(t, 1H, J=6.5 Hz), 3.50-3.58(m, 1H), 3.35-3.42(m, 1H), 3.17(s, 3H), 3.00-3.06(m, 2H), 1.85-1.95(m, 2H), 1.79(s, 3H), 0.90(s, 9H).

Example 498
Synthesis of (E)-3-[2,6-dichloro-4-(4-{3-[3-(2,2-dimethylpropyloxy)-1-methyloxypropyl]-2-fluorophenyl}thiazol-2-ylcarbamoyl)phenyl]-2-methylacrylic acid (B2007)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 8.29(s, 2H), 8.01(t, 1H, J=7.5 Hz), 7.64(s, 1H), 7.30-7.40(m, 3H), 4.72(t, 1H, J=6.5 Hz), 3.50-3.58(m, 1H), 3.35-3.42(m, 1H), 3.17(s, 3H), 3.00-3.06(m, 2H), 1.85-1.95(m, 2H), 1.69(s, 3H), 0.90(s, 9H).

Example 499
Synthesis of (Z)-3-[4-(4-{3-[3-(2,2-dimethylpropyloxy)-1-methyloxypropyl]-2-fluorophenyl}thiazol-2-ylcarbamoyl)-2,6-difluorophenyl]-2-methyloxyacrylic acid (B2008)

Example 500
Synthesis of (Z)-3-[2,6-dichloro-4-(4-{3-[3-(2,2-dimethylpropyloxy)-1-methyloxypropyl]-2-fluorophenyl}thiazol-2-ylcarbamoyl)phenyl]-2-methyloxyacrylic acid (B2009)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 8.29(s, 2H), 8.01(t, 1H, J=7.5 Hz), 7.64(s, 1H), 7.30-7.40(m, 2H), 6.65(s, 1H), 4.72(t, 1H, J=6.5 Hz), 3.61(s, 3H), 3.50-3.58(m, 1H), 3.35-3.42(m, 1H), 3.17(s, 3H), 3.00-3.06(m, 2H), 1.85-1.95(m, 2H), 0.90(s, 9H).

Example 501
Synthesis of (E)-3-(2,6-difluoro-4-{4-[2-fluoro-3-(3-isopropyloxy-1-methyloxypropyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B2010)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 8.06(t, 1H, J=7.5 Hz), 7.96(s, 1H), 7.93(s, 1H), 7.64(s, 1H), 7.30-7.40(m, 3H), 4.72(t, 1H, J=6.5 Hz), 3.50-3.58(m, 1H), 3.35-3.42(m, 2H), 3.17(s, 3H), 1.79-1.95(m, 2H), 1.79(s, 3H), 1.05(d, 6H, J=6.0 Hz).

Example 502
Synthesis of (E)-3-(2,6-dichloro-4-{4-[2-fluoro-3-(3-isopropyloxy-1-methyloxypropyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B2011)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 8.29(s, 2H), 8.06(t, 1H, J=7.5 Hz), 7.64(s, 1H), 7.30-7.40(m, 3H), 4.72(t, 1H, J=6.5 Hz), 3.50-3.58(m, 1H), 3.35-3.42(m, 2H), 3.17(s, 3H), 1.80-1.98(m, 2H), 1.68(s, 3H), 1.05(d, 6H, J=6.0 Hz).

Example 503
Synthesis of (Z)-3-(2,6-difluoro-4-{4-[2-fluoro-3-(3-isopropyloxy-1-methyloxypropyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methyloxyacrylic acid (B2012)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 8.06(t, 1H, J=7.5 Hz), 7.96(s, 1H), 7.93(s, 1H), 7.64(s, 1H), 7.30-7.40(m, 2H), 6.65(s, 1H), 4.72(t, 1H, J=6.5 Hz), 3.71(s, 3H), 3.50-3.58(m, 1H), 3.35-3.42(m, 2H), 3.17(s, 3H), 1.80-1.98(m, 2H), 1.05(d, 6H, J=6.0 Hz).

Example 504
Synthesis of (E)-3-(2,6-difluoro-4-{4-[2-fluoro-3-(4-methylpentyloxymethyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B2013)

1H-NMR(DMSO-d6) 13.02(bs, 2H), 8.04(dt, 1H, J=1.8, 7.5 Hz), 7.92-8.00(m, 2H), 7.65(d, 1H, J=2.4 Hz), 7.39-7.45(m, 1H), 7.28-7.36(m, 2H), 4.58(s, 2H), 3.48(t, 2H, J=6.6 Hz), 1.81(d, 3H, J=1.8 Hz), 1.46-1.60(m, 3H), 1.17-1.25(m, 2H), 0.86(d, 6H, J=6.6 Hz).

Example 505
Synthesis of (Z)-3-(2,6-difluoro-4-{4-[2-fluoro-3-(4-methylpentyloxymethyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methyloxyacrylic acid (B2014)

1H-NMR(DMSO-d6) 12.97(bs, 1H), 8.04(dt, 1H, J=1.8, 7.5 Hz), 7.86-7.96(m, 2H), 7.65(d, 1H, J=2.7 Hz), 7.38-7.46(m, 1H), 7.31(t, 1H, J=7.8 Hz), 6.64(s, 1H), 4.58(s, 2H), 3.71(s, 3H), 3.48(t, 2H, J=6.6 Hz), 1.45-1.62(m, 3H), 1.17-1.20(m, 2H), 0.86(d, 6H, J=6.6 Hz).

Example 506
Synthesis of (E)-3-(2,6-dichloro-4-{4-[2-fluoro-3-(4-methylpentyloxymethyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B2015)

1H-NMR(DMSO-d6) 13.02(bs, 2H), 8.29(s, 2H), 8.04(dt, 1H, J=1.8, 7.2 Hz), 7.65(d, 1H, J=2.7 Hz), 7.38-7.46(m, 2H), 7.31(t, 1H, J=7.5 Hz), 4.58(s, 2H), 3.48(t, 2H, J=6.6 Hz), 1.69(s, 3H), 1.46-1.60(m, 3H), 1.17-1.25(m, 2H), 0.86(d, 6H, J=6.6 Hz).

Example 507
Synthesis of (Z)-3-(2,6-dichloro-4-{4-[2-fluoro-3-(4-methylpentyloxymethyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methyloxyacrylic acid (B2016)

1H-NMR(DMSO-d6) 13.01(bs, 1H), 8.25(s, 2H), 8.04(dt, 1H, J=1.5, 7.5 Hz), 7.65(d, 1H, J=2.7 Hz), 7.39-7.46(m, 1H), 7.31(t, 1H, J=7.8 Hz), 6.73(s, 1H), 4.58(s, 2H), 3.61(s, 3H), 3.48(t, 2H, J=6.3 Hz), 1.46-1.60(m, 3H), 1.15-1.27(m, 2H), 0.86(d, 6H, J=6.6 Hz).

Example 508
Synthesis of (E)-3-{2,6-difluoro-4-[4-(2-fluoro-3-methyloxyphenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methylacrylic acid (B2017)

1H-NMR(DMSO-d6) 13.0(bs, 2H), 7.98(s, 1H), 7.95(s, 1H), 7.60-7.68(m, 2H), 7.34(bs, 1H), 7.14-7.28(m, 2H), 3.89(s, 3H), 1.81(s, 3H).

Example 509
Synthesis of (E)-3-{2,6-dichloro-4-[4-(2-fluoro-3-methyloxyphenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methylacrylic acid (B2018)

1H-NMR(DMSO-d6) 13.0(bs, 2H), 8.29(s, 2H), 7.59-7.68(m, 2H), 7.40(s, 1H), 7.14-7.28(m, 2H), 3.89(s, 3H), 1.69(s, 3H).

Example 510
Synthesis of (Z)-3-{2,6-dichloro-4-[4-(2-fluoro-3-methyloxyphenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methyloxyacrylic acid (B2019)

1H-NMR(DMSO-d6) 13.6(bs, 1H), 13.0(bs, 1H), 8.25(s, 2H), 7.60-7.68(m, 2H), 7.14-7.26(m, 2H), 6.74(s, 1H), 3.89(s, 3H), 3.61(s, 3H).

Example 511
Synthesis of (E)-3-(4-{4-[3-(2,2-dimethylpropyloxymethyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methyloxyacrylic acid (B2020)

1H NMR(DMSO-d6) 12.93(bs, 2H), 7.90-7.99(m, 3H), 7.74(s, 1H), 7.39-7.41(m, 1H), 7.25(t, 1H, J=7.5 Hz), 6.65(s, 1H), 4.60(s, 2H), 3.72(s, 3H), 3.3.66(s, 3H), 3.19(s, 2H), 0.92(s, 9H).

Example 512
Synthesis of (E)-3-(2,6-dichloro-4-{4-[3-(2,2-dimethylpropyloxymethyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B2021)

1H NMR(DMSO-d6) 12.98(bs, 2H), 8.29(s, 2H), 7.98(dd, 1H, J=1.5 Hz, 7.5 Hz), 7.74(s, 1H), 7.39-7.41(m, 2H), 7.25(t, 1H, J=7.5 Hz), 4.60(s, 2H), 3.66(s, 3H), 3.19(s, 2H), 1.69(d, 3H, J=1.2 Hz), 0.92(s, 9H).

Example 513
Synthesis of (Z)-3-(2,6-dichloro-4-{4-[3-(2,2-dimethylpropyloxymethyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methyloxyacrylic acid (B2022)

1H NMR(DMSO-d6) 12.96(bs, 2H), 8.25(s, 2H), 7.97(dd, 1H, J=1.5 Hz, 7.5 Hz), 7.74(s, 1H), 7.40(dd, 1H, J=1.5 Hz, 7.5 Hz), 7.25(t, 1H, J=7.5 Hz), 6.73(s, 1H), 4.60(s, 2H), 3.66(s, 3H), 3.62(s, 3H), 3.19(s, 2H), 0.92(s, 9H).

Example 514
Synthesis of (E)-3-(4-{4-[3-(2-ethylbutyloxymethyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methyl acrylic acid (B2023)

1H NMR(DMSO-d6) 12.98(bs, 2H), 7.95-7.99(m, 3H), 7.74(s, 1H), 7.37-7.39(dd, 1H, J=1.8 Hz, 7.8 Hz), 7.34(s, 1H), 7.24(t, 1H, J=7.5 Hz), 4.56(s, 2H), 3.65(s, 3H), 3.42(d, 2H, J=5.7 Hz), 1.81(s, 3H), 1.26-1.51(m, 5H), 0.85(t, 6H, J=7.5 Hz).

Example 515
Synthesis of (Z)-3-(4-{4-[3-(2-ethylbutyloxymethyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methyloxyacrylic acid (B2024)

1H NMR(DMSO-d6) 12.93(bs, 2H), 7.90-7.99(m, 3H), 7.74(s, 1H), 7.37-7.40(m, 1H), 7.24(t, 1H, J=7.5 Hz),6.65(s, 1H), 4.56(s, 2H), 3.72(s, 3H), 3.65(s, 3H), 3.42(d, 2H, J=5.4 Hz), 1.24-1.49(m, 5H), 0.85(t, 6H, J=7.5 Hz).

Example 516
Synthesis of (E)-3-(2,6-dichloro-4-{4-[3-(2-ethylbutyloxymethyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B2025)

1H NMR(DMSO-d6) 13.00(bs, 2H), 8.29(s, 2H), 7.97(dd, 1H, J=1.5 Hz, 7.5 Hz), 7.74(s, 1H), 7.37-7.41(m, 2H), 7.25(t, 1H, J=7.5 Hz), 4.57(s, 2H), 3.66(s, 3H), 3.42(d, 2H, J=5.7 Hz), 1.69(s, 3H), 1.25-1.49(m, 5H), 0.86(t, 6H, J=7.5 Hz).

Example 517
Synthesis of (Z)-3-(2,6-dichloro-4-{4-[3-(2-ethylbutyloxymethyl)-2-methyloxyphenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methyloxyacrylic acid (B2026)

1H NMR(DMSO-d6) 12.95(bs, 2H), 8.25(s, 2H), 7.97(d, 1H, J=8.1 Hz), 7.73(s, 1H), 7.38(d, 1H, J=6.0 Hz), 7.24(t, 1H, J=7.5 Hz), 6.73(s, 1H), 4.57(s, 2H), 3.66(s, 3H), 3.62(s, 3H), 3.42(d, 2H, J=5.7 Hz), 1.24-1.49(m, 5H), 0.85(t, 6H, J=7.5 Hz).

Example 518
Synthesis of (E)-3-(2,6-difluoro-4-{4-[2-methyloxy-3-(3-methylbutyloxymethyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B2027)

1H NMR(DMSO-d6) 12.94(bs, 2H), 7.95-7.99(m, 3H), 7.74(s, 1H), 7.34-7.40(m, 2H), 7.24(t, 1H, J=7.5 Hz), 4.56(s, 2H), 3.65(s, 3H), 3.54(t, 2H, J=6.3 Hz), 1.81(s, 3H), 1.66-1.71(m, 1H), 1.47(q, 2H, 6.6 Hz), 0.89(d, 6H, J=6.6 Hz).

Example 519
Synthesis of (E)-3-(2,6-dichloro-4-{4-[2-methyloxy-3-(3-methylbutyloxymethyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B2028)

1H NMR(DMSO-d6) 12.97(bs, 2H), 8.29(s, 2H), 7.97(dd, 1H, J=9.3 Hz), 7.73(s, 1H), 7.37-7.41(m, 2H), 7.24(t, 1H, J=7.5 Hz), 4.56(s, 2H), 3.66(s, 3H), 3.54(t, 2H, J=6.6 Hz), 1.66-1.75(m, 1H), 1.69(s, 3H), 1.47(q, 2H, 6.6 Hz), 0.89(d, 6H, J=6.6 Hz).

Example 520
Synthesis of (E)-3-(4-{4-[3-(3,3-dimethylbutyloxymethyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methylacrylic acid (B2029)

1H-NMR(DMSO-d6) 13.04(bs, 2H), 8.00-8.08(m, 1H), 7.92-8.08(m, 2H), 7.65(d, 1H, J=1.8 Hz), 7.39-7.46(m, 1 Hz), 7.28-7.36(m, 2H), 4.58(s, 2H), 3.56(t, 2H, J=7.2 Hz), 1.81(s, 3H), 1.51(t, 2H, J=7.2 Hz), 0.91(s, 9H).

Example 521
Synthesis of (Z)-3-(4-{4-[3-(3,3-dimethylbutyloxymethyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methyloxyacrylic acid (B2030)

1H-NMR(DMSO-d6) 12.99(bs, 1H), 8.00-8.07(m, 1H), 7.86-7.96(m, 2H), 7.65(d, 1H, J=2.4 Hz), 7.39-7.46(m, 1H), 7.31(t, 1H, J=7.5 Hz), 6.65(s, 1H), 4.58(s, 2H), 3.71(s, 3H), 3.56(t, 2H, J=7.2 Hz), 1.51(t, 3H, J=7.2 Hz), 0.90(s, 9H).

Example 522
Synthesis of (E)-3-(2,6-dichloro-4-{4-[3-(3,3-dimethylbutyloxymethyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B2031)

1H-NMR(DMSO-d6) 13.02(bs, 2H), 8.29(s, 2H), 8.00-8.08(m, 1H), 7.65(d, 1H, J=2.1 Hz), 7.39-7.48(m, 2H), 7.31(t, 1H, J=7.5 Hz), 4.58(s, 2H), 3.56(t, 2H, J=7.2 Hz), 1.69(s, 3H), 1.51(t, 2H, J=7.2 Hz), 0.91(s, 9H).

Example 523
Synthesis of (Z)-3-(2,6-dichloro-4-{4-[3-(3,3-dimethylbutyloxymethyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methyloxyacrylic acid (B 2032)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 8.25(s, 2H), 8.00-8.08(m, 1H), 7.66(d, 1H, J=2.4 Hz), 7.39-7.46(m, 1H), 7.31(t, 1H, J=7.5 Hz), 6.73(s, 1H), 4.59(s, 2H), 3.62(s, 3H), 3.56(t, 2H, J=7.2 Hz), 1.51(t, 2H, J=7.2 Hz), 0.91(s, 9H).

Example 524
Synthesis of (E)-3-{4-[4-(3-cyclohexylmethyloxymethyl-2-fluorophenyl)thiazol-2-ylcarbamoyl]-2,6-difluorophenyl}-2-methylacrylic acid (B2033)

1H-NMR(DMSO-d6) 13.04(bs, 2H), 7.92-8.08(m, 3H), 7.65(d, 1H, J=2.4 Hz), 7.39-7.46(m, 1 Hz), 7.28-7.36(m, 2H), 4.58(s, 2H), 1.81(s, 3H), 1.54-1.79(m, 6H), 1.10-1.25(m, 3H), 0.80-1.02(m, 2H).

Example 525
Synthesis of (Z)-3-{4-[4-(3-cyclohexylmethyloxymethyl-2-fluorophenyl)thiazol-2-ylcarbamoyl]-2,6-difluorophenyl}-2-methyloxyacrylic acid (B2034)

1H-NMR(DMSO-d6) 12.98(bs, 1H), 8.04(dt, 1H, J=2.1, 7.5 Hz), 7.70-7.96(m, 2H), 7.65(d, 1H, J=2.7 Hz), 7.39-7.46(m, 1H), 7.31(t, 1H, J=7.8 Hz), 6.66(s, 1H), 4.58(s, 2H), 3.72(s, 3H), 1.52-1.79(m, 6H), 1.06-1.28(m, 3H), 0.83-1.02(m, 2H).

Example 526
Synthesis of (E)-3-{2,6-dichloro-4-[4-(3-cyclohexylmethyloxymethyl-2-fluorophenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methylacrylic acid (B2035)

1H-NMR(DMSO-d6) 13.02(bs, 2H), 8.29(s, 2H), 8.04(dt, 1H, J=1.8, 7.8 Hz), 7.65(d, 1H, J=2.4 Hz), 7.38-7.46(m, 2H), 7.31(t, 1H, J=7.8 Hz), 4.58(s, 2H), 1.50-1.80(m, 6H), 1.07-1.30(m, 3H), 0.82-1.05(m, 2H).

Example 527
Synthesis of (Z)-3-{2,6-dichloro-4-[4-(3-cyclohexylmethyloxymethyl-2-fluorophenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methyloxyacrylic acid (B2036)

1H-NMR(DMSO-d6) 13.02(bs, 1H), 8.25(s, 2H), 8.00-8.08(m, 1H), 7.65(d, 1H, J=2.4 Hz), 7.39-7.46(m, 1H), 7.31(t, 1H, J=8.1 Hz), 6.72(s, 1H), 4.58(s, 2H), 3.62(s, 3H), 1.50-1.78(m, 6H), 1.08-1.30(m, 3H), 0.86-1.00(m, 2H).

Example 528
Synthesis of (E)-3-(4-{4-[3-(2-ethylsufanylethyloxymethyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methylacrylic acid (B2037)

1H-NMR(DMSO-d6) 13.02(bs, 2H), 8.05(dt, 1H, J=1.8, 7.5 Hz), 7.92-8.05(m, 2H), 7.65(d, 1H, J=2.7 Hz), 7.42-7.48(m, 1 Hz), 7.28-7.35(m, 2H), 4.64(s, 2H), 3.66(t, 2H, J=6.6 Hz), 2.73(t, 2H, J=6.9 Hz), 2.50-2.59(m, 2H), 1.81(s, 3H), 1.17(t, 3H, J=7.5 Hz).

Example 529
Synthesis of (Z)-3-(4-{4-[3-(2-ethylsufanylethyloxymethyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methyloxyacrylic acid (B2038)

1H-NMR(DMSO-d6) 12.98(bs, 1H), 8.05(dt, 1H, J=1.8, 7.8 Hz), 7.70-7.95(m, 2H), 7.66(d, 1H, J=2.7 Hz), 7.42-7.49(m, 1H), 7.32(t, 1H, J=7.8 Hz), 6.66(s, 1H), 4.64(s, 2H), 3.71(s, 3H), 3.66(t, 2H, J=6.6 Hz), 2.73(t, 2H, J=6.6 Hz), 2.50-2.59(m, 2H), 1.17(t, 3H, J=7.5 Hz).

Example 530
Synthesis of (E)-3-(2,6-dichloro-4-{4-[3-(2-ethylsufanylethyloxymethyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B2039)

1H-NMR(DMSO-d6) 13.02(bs, 2H), 8.29(s, 2H), 8.05(dt, 1H, J=1.8, 7.8 Hz), 7.65(d, 1H, J=2.7 Hz), 7.42-7.48(m, 1H), 7.40(d, 1H, J=1.2 Hz), 7.31(t, 1H, J=7.5 Hz), 4.64(s, 2H), 3.66(t, 2H, J=6.6 Hz), 2.73(t, 2H, J=6.9 Hz), 2.50-2.59(m, 2H), 1.69(s, 3H), 1.17(t, 3H, J=7.5 Hz).

Example 531
Synthesis of (Z)-3-(2,6-dichloro-4-{4-[3-(2-ethylsufanylethyloxymethyl)-2-fluorophenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methyloxyacrylic acid (B2040)

1H-NMR(DMSO-d6) 13.01(bs, 1H), 8.24(s, 2H), 8.05(dt, 1H, J=1.8, 7.5 Hz), 7.65(d, 1H, J=2.4 Hz), 7.42-7.49(m, 1H), 7.32(t, 1H, J=7.5 Hz), 6.73(s, 1H), 4.64(s, 2H), 3.66(t, 2H, J=6.6 Hz), 3.61(s, 3H), 2.73(t, 2H, J=6.9 Hz), 2.50-2.59(m, 2H), 1.17(t, 3H, J=7.5 Hz).

Example 532
Synthesis of (E)-3-{2,6-difluoro-4-[4-(2-methyloxy-3-nonyloxyphenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methylacrylic acid (B2041)

1H-NMR(DMSO-d6) 12.92 (bs, 2H), 7.93-7.97 (m, 2H), 7.75 (s, 1H), 7.63-7.66 (m, 1H), 7.34 (s, 1H), 7.08-7.15 (m, 1H), 7.02-7.04 (m, 1H), 4.02 (t, 1H, J=6.3 Hz), 3.80 (s, 3H), 1.73-1.81 (m, 5H), 1.43-1.50 (m, 2H), 1.26-1.38 (m, 10H), 0.84-0.88 (m, 3H).

Example 533
Synthesis of (E)-3-{2,6-dichloro-4-[4-(2-methyloxy-3-nonyloxyphenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methylacrylic acid (B2042)

1H-NMR(DMSO-d6) 12.94 (bs, 2H), 8.28 (s, 2H), 7.74 (s, 1H), 7.63-7.66 (m, 1H), 7.40 (s, 1H), 7.10-7.15 (m, 1H), 7.02-7.04 (m, 1H), 4.03 (t, 1H, J=6.3 Hz), 3.80 (s, 3H), 1.73-1.81 (m, 2H), 1.69 (s, 3H), 1.43-1.50 (m, 2H), 1.26-1.38 (m, 10H), 0.84-0.88 (m, 3H).

Example 534
Synthesis of (E)-3-(2,6-difluoro-4-{4-[2-methyloxy-3-(4-methylpentyloxy)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B2043)

1H-NMR(DMSO-d6) 12.93 (bs, 2H), 7.95-7.97 (m, 2H), 7.75 (s, 1H), 7.63-7.66 (m, 1H), 7.34 (s, 1H), 7.10-7.15 (m, 1H), 7.02-7.04 (m, 1H), 4.02 (t, 1H, J=6.3 Hz), 3.80 (s, 3H), 1.74-1.81 (m, 5H), 1.58-1.67 (m, 1H), 1.33-1.41 (m, 2H), 0.91 (d, 6H, J=5.5 Hz).

Example 535
Synthesis of (E)-3-(2,6-dichloro-4-{4-[2-methyloxy-3-(4-methylpentyloxy)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B2044)

1H-NMR(DMSO-d6) 12.93 (bs, 2H), 8.28 (s, 2H), 7.74 (s, 1H), 7.63-7.66 (m, 1H), 7.40 (s, 1H), 7.10-7.15 (m, 1H), 7.01-7.04 (m, 1H), 4.02 (t, 1H, J=6.3 Hz), 3.80 (s, 3H), 1.74-1.82 (m, 2H), 1.69 (s, 3H), 1.58-1.67 (m, 1H), 1.33-1.41 (m, 2H), 0.91 (d, 6H, J=5.5 Hz).

Example 536
Synthesis of (E)-3-{2,6-difluoro-4-[4-(3-hexyloxy-2-methyloxyphenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methylacrylic acid (B2045)

1H-NMR(DMSO-d6) 12.96 (bs, 2H), 7.93-7.97 (m, 2H), 7.75 (s, 1H), 7.63-7.66 (m, 1H), 7.34 (s, 1H), 7.10-7.15 (m, 1H), 7.01-7.04 (m, 1H), 4.03 (t, 1H, J=6.3 Hz), 3.80 (s, 3H), 1.74-1.81 (m, 5H), 1.44-1.53 (m, 2H), 1.32-1.37 (m, 4H), 0.87-0.92 (m, 3H).

Example 537
Synthesis of (E)-3-{2,6-dichloro-4-[4-(3-hexyloxy-2-methyloxyphenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methylacrylic acid (B2046)

1H-NMR(DMSO-d6) 12.93 (bs, 2H), 8.27 (s, 2H), 7.72 (s, 1H), 7.62-7.64 (m, 1H), 7.38 (s, 1H), 7.08-7.13 (m, 1H), 7.00-7.03 (m, 1H), 4.02 (t, 1H, J=6.3 Hz), 3.78 (s, 3H), 1.72-1.81 (m, 2H), 1.67 (s, 3H), 1.42-1.51 (m, 2H), 1.32-1.37 (m, 4H), 0.87-0.92 (m, 3H).

Example 538
Synthesis of (E)-3-(2,6-difluoro-4-{4-[2-methyloxy-3-(1-methyloxy-4-methylpentyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B2047)

1H-NMR(DMSO-d6) 12.97 (bs, 2H), 7.89-7.97 (m, 3H), 7.72 (s, 1H), 7.24-7.34 (m, 3H), 4.53-4.57 (m, 1H), 3.61 (s, 3H), 3.16 (s, 3H), 1.81 (s, 3H), 0.87-1.72 (m, 11H).

Example 539
Synthesis of (E)-3-(2,6-dichloro-4-{4-[2-methyloxy-3-(1-methyloxy-4-methylpentyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B2049)

1H-NMR(DMSO-d6) 12.98 (bs, 2H), 9.29 (s, 1H), 7.89-7.92 (m, 1H), 7.72 (s, 1H), 7.41 (s, 1H), 7.24-7.37 (m, 3H), 4.53-4.57 (m, 1H), 3.61 (s, 3H), 3.16 (s, 3H), 0.87-1.72 (m, 14H).

Example 540
Synthesis of (E)-3-{2,6-dichloro-4-[4-(2-fluoro-3-propyloxyphenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methylacrylic acid (B2051)

1H-NMR(DMSO-d6) 13.0(bs, 2H), 7.98(s, 1H), 7.95(s, 1H), 7.59-7.67(m, 2H), 7.34(bs, 1H), 7.12-7.25(m, 2H), 4.05(t, 2H, J=6.6 Hz), 1.74-1.84(m, 5H), 1.01(t, 3H, J=7.2 Hz).

Example 541
Synthesis of (E)-3-{2,6-dichloro-4-[4-(2-fluoro-3-propyloxyphenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methylacrylic acid (B2052)

1H-NMR(DMSO-d6) 13.0(bs, 2H), 8.29(s, 2H), 7.60-7.66(m, 2H), 7.41(s, 1H), 7.13-7.26(m, 2H), 4.06(t, 2H, J=6.6 Hz), 1.79(q, 2H, J=6.9 Hz), 1.70(s, 3H), 1.02(t, 3H, J=7.5 Hz).

Example 542
Synthesis of (Z)-3-{2,6-difluoro-4-[4-(2-fluoro-3-propyloxyphenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methyloxyacrylic acid (B2053)

1H-NMR(DMSO-d6) 13.0(bs, 2H), 7.92(s, 1H), 7.89(s, 1H), 7.60-7.67(m, 2H), 7.14-7.25(m, 2H), 6.62-6.70(m, 1H), 4.05(t, 2H, J=6.3 Hz), 3.71(s, 3H), 1.78(q, 2H, J=6.3 Hz), 1.01(t, 3H, J=7.2 Hz).

Example 543
Synthesis of (Z)-3-{2,6-dichloro-4-[4-(2-fluoro-3-propyloxyphenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methyloxyacrylic acid (B2054)

1H-NMR(DMSO-d6) 13.0(bs, 2H), 8.25(s, 2H), 7.59-7.66(m, 2H), 7.13-7.26(m, 2H), 6.73(s, 2H), 4.05(t, 2H, J=6.6 Hz), 3.61(s, 3H), 1.78(q, 2H, J=6.9 Hz), 1.01(t, 3H, J=7.2 Hz).

Example 544
Synthesis of (E)-3-{2,6-difluoro-4-[4-(2-fluoro-3-pentyloxyphenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methylacrylic acid (B2055)

1H-NMR(DMSO-d6) 13.0(bs, 2H), 7.97(s, 1H), 7.95(s, 1H), 7.59-7.67(m, 2H), 7.34(bs, 1H), 7.13-7.25(m, 2H), 4.08(t, 2H, J=6.6 Hz), 1.72-1.82(m, 5H), 1.33-1.50(m, 4H), 0.91(t, 3H, J=7.2 Hz).

Example 545
Synthesis of (E)-3-{2,6-dichloro-4-[4-(2-fluoro-3-pentyloxyphenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methylacrylic acid (B2056)

1H-NMR(DMSO-d6) 13.0(bs, 2H), 8.28(s, 2H), 7.59-7.66(m, 2H), 7.40(bs, 1H), 7.12-7.25(m, 2H), 4.08(t, 2H, J=6.6 Hz), 1.71-1.82(m, 2H), 1.69(s, 3H), 1.30-1.51(m, 4H), 0.91(t, 3H, J=7.2 Hz).

Example 546
Synthesis of (Z)-3-{2,6-difluoro-4-[4-(2-fluoro-3-pentyloxyphenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methyloxyacrylic acid (B 2057)

1H-NMR(DMSO-d6) 13.0(bs, 2H), 7.93(s, 1H), 7.89(s, 1H), 7.59-7.65(m, 2H), 7.12-7.24(m, 2H), 6.65(s, 1H), 4.08(t, 2H, J=6.6 Hz), 3.71(s, 3H), 1.71-1.80(m, 2H), 1.35-1.50(m, 4H), 0.91(t, 3H, J=7.2 Hz).

Example 547
Synthesis of (Z)-3-{2,6-dichloro-4-[4-(2-fluoro-3-pentyloxyphenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methylacrylic acid (B2058)

1H-NMR(DMSO-d6) 13.0(bs, 2H), 8.24(s, 2H), 7.58-7.65(m, 2H), 7.12-7.25(m, 2H), 6.73(s, 1H), 4.08(t, 2H, J=6.6 Hz), 3.61(s, 3H), 1.72-1.82(m, 2H), 1.33-1.48(m, 4H), 0.91(t, 3H, J=6.9 Hz).

Example 548
Synthesis of (E)-3-{2,6-difluoro-4-[4-(2-fluoro-3-hexyloxyphenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methylacrylic acid (B2059)

1H-NMR(DMSO-d6) 13.0(bs, 2H), 7.98(s, 1H), 7.95(s, 1H), 7.59-7.66(m, 2H), 7.34(s, 1H), 7.13-7.24(m, 2H), 4.08(t, 2H, J=6.6 Hz), 1.71-1.84(m, 5H), 1.30-1.51(m, 6H), 0.89(t, 3H, J=7.2 Hz).

Example 549
Synthesis of (E)-3-{2,6-dichloro-4-[4-(2-fluoro-3-hexyloxyphenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methylacrylic acid (B2060)

1H-NMR(DMSO-d6) 13.0(bs, 2H), 8.29(s, 2H), 7.59-7.65(m, 2H), 7.41(s, 1H), 7.13-7.25(m, 2H), 4.08(t, 2H, J=6.6 Hz), 1.70-1.80(m, 2H), 1.69(s, 3H), 1.30-1.50(m, 6H), 0.89(t, 3H, J=6.9 Hz).

Example 550
Synthesis of (Z)-3-{2,6-difluoro-4-[4-(2-fluoro-3-hexyloxyphenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methyloxyacrylic acid (B2061)

1H-NMR(DMSO-d6) 13.6(bs, 1H), 13.0(bs, 1H), 7.93(s, 1H), 7.90(s, 1H), 7.59-7.66(m, 2H), 7.12-7.25(m, 2H), 6.66(s, 1H), 4.08(t, 2H, J=6.6 Hz), 3.71(s, 3H), 1.71-1.80(m, 2H), 1.29-1.50(m, 6H), 0.89(t, 3H, J=7.2 Hz).

Example 551
Synthesis of (Z)-3-{2,6-dichloro-4-[4-(2-fluoro-3-hexyloxyphenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methyloxyacrylic acid (B2062)

1H-NMR(DMSO-d6) 13.6(bs, 1H), 13.0(bs, 1H), 8.25(s, 2H), 7.59-7.66(m, 2H), 7.12-7.25(m, 2H), 6.74(s, 1H), 4.08(t, 2H, J=6.6 Hz), 3.61(s, 3H), 1.70-1.81(m, 2H), 1.30-1.50(m, 6H), 0.89(t, 3H, J=6.9 Hz).

Example 552
Synthesis of (E)-3-{2,6-difluoro-4-[4-(2-fluoro-3-heptyloxyphenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methylacrylic acid (B2063)

1H-NMR(DMSO-d6) 13.0(bs, 2H), 7.98(s, 1H), 7.95(s, 1H), 7.59-7.66(m, 2H), 7.34(bs, 1H), 7.13-7.25(m, 2H), 4.08(t, 2H, J=6.3 Hz), 1.73-1.82(m, 5H), 1.28-1.50(m, 8H), 0.88(t, 3H, J=7.5 Hz).

Example 553
Synthesis of (E)-3-{2,6-dichloro-4-[4-(2-fluoro-3-heptyloxyphenyl)thiazol-2-ylcarbamoyl)phenyl]-2-methylacrylic acid (B2064)

1H-NMR(DMSO-d6) 13.0(bs, 2H), 8.29(s, 2H), 7.59-7.67(m, 2H), 7.40(s, 1H), 7.13-7.24(m, 2H), 4.08(t, 2H, J=6.3 Hz), 1.70-1.80(m, 2H), 1.69(s, 3H), 1.23-1.50(m, 8H), 0.88(t, 3H, J=6.9 Hz).

Example 554
Synthesis of (Z)-3-{2,6-difluoro-4-[4-(2-fluoro-(3-heptyloxyphenyl)thiazol-2-ylcarbamoyl)phenyl]-2-methyloxyacrylic acid (B2065)

1H-NMR(DMSO-d6) 13.0(bs, 2H), 7.92(s, 1H), 7.89(s, 1H), 7.60-7.65(m, 2H), 7.13-7.25(m, 2H), 6.61(s, 1H), 4.08(t, 2H, J=6.0Hz), 3.72(s, 3H), 1.71-1.80(m, 2H), 1.27-1.50(m, 8H), 0.88(t, 3H, J=6.9 Hz).

Example 555
Synthesis of (Z)-3-{2,6-dichloro-4-[4-(2-fluoro-3-heptyloxyphenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methyloxyacrylic acid (B 2066)

1H-NMR(DMSO-d6) 13.6(bs, 1H), 13.0(bs, 1H), 8.25(s, 2H), 7.59-7.66(m, 2H), 7.12-7.24(m, 2H), 6.74(s, 1H), 4.08(t, 2H, J=6.6 Hz), 3.62(s, 3H), 1.70-1.81(m, 2H), 1.26-1.50(m, 8H), 0.88 (t, 3H, J=6.6 Hz).

Example 556
Synthesis of (E)-3-(2,6-difluoro-4-{4-[2-fluoro-(3-methylbutyloxy)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B2067)

1H-NMR(DMSO-d6) 13.0(bs, 2H), 7.98(s, 1H), 7.95(s, 1H), 7.60-7.67(m, 2H), 7.34(s, 1H), 7.15-7.25(m, 2H), 4.12(t, 2H, J=6.6 Hz), 1.63-1.87(m, 6H), 0.96(d, 6H, J=6.6 Hz).

Example 557
Synthesis of (Z)-3-(2,6-difluoro-4-{4-[2-fluoro-(3-methylbutyloxy)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methyloxyacrylic acid (B2068)

1H-NMR(DMSO-d6) 13.6(bs, 1H), 13.0(bs, 1H), 7.93(s, 1H), 7.90(s, 1H), 7.60-7.68(m, 2H), 7.15-7.26(m, 2H), 6.66(s, 1H), 4.12(t, 2H, J=6.6Hz), 3.71(s, 3H), 1.76-1.80(m, 1H), 1.63-1.71(m, 2H), 0.96(d, 6H, J=6.6 Hz).

Example 558
Synthesis of (Z)-3-(2,6-dichloro-4-{4-[2-fluoro-3-(3-methylbutyloxy)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methyloxyacrylic acid (B2069)

1H-NMR(DMSO-d6) 13.6(bs, 1H), 13.0(bs, 1H), 8.25(s, 2H), 7.60-7.66(m, 2H), 7.15-7.26(m, 2H), 6.74(s, 1H), 4.12(t, 2H, J=6.6 Hz), 3.62(s, 3H), 1.76-1.90(m, 1H), 1.63-1.71(m, 2H), 0.97(d, 6H, J=6.6 Hz).

Example 559
Synthesis of (E)-3-(4-{4-[3-(2-cyclohexylethyloxy)-2-fluorophenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methylacrylic acid (B2070)

1H-NMR(DMSO-d6) 13.0(bs, 2H), 7.98(s, 1H), 7.95(s, 1H), 7.59-7.66(m, 2H), 7.34(s, 1H), 7.14-7.24(m, 2H), 4.12(t, 2H, J=6.6 Hz), 1.41-1.83(m, 11H), 0.88-1.31(m, 5H).

Example 560
Synthesis of (E)-3-(2,6-dichloro-4-{4-[3-(2-cyclohexylethyloxy)-2-fluorophenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B 2071)

1H-NMR(DMSO-d6) 13.0(bs, 2H), 8.29(s, 2H), 7.59-7.67(m, 2H), 7.40(s, 1H), 7.14-7.25(m, 2H), 4.12(t, 2H, J=6.6 Hz), 1.46-1.70(m, 11H), 0.91-1.30(m, 5H).

Example 561
Synthesis of (Z)-3-(4-{4-[3-(2-cyclohexylethyloxy)-2-fluorophenyl]thiazol-2-ylcarbamoyl)-2,6-difluorophenyl)-2-methyloxyacrylic acid (B2072)

1H-NMR(DMSO-d6) 13.0(bs, 2H), 7.92(s, 1H), 7.89(s, 1H), 7.59-7.66(m, 2H), 7.13-7.25(m, 2H), 6.61(s, 1H), 4.12(t, 2H, J=6.6 Hz), 3.72(s, 3H), 1.46-1.80(m, 8H,), 0.91-1.30(m, 5H).

Example 562
Synthesis of (Z)-3-{2,6-dichloro-4-[4-(3-cyclohexylmethyloxy-2-fluorophenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methyloxyacrylic acid (B2073)

1H-NMR(DMSO-d6) 13.0(bs, 2H), 8.25(s, 2H), 7.59-7.66(m, 2H), 7.14-7.24(m, 2H), 6.73(s, 1H), 4.12(t, 2H, J=6.6 Hz), 3.61(s, 3H), 1.46-1.71(m, 8H), 0.95-1.30(m, 5H).

Example 563
Synthesis of (E)-3-{4-[4-(3-cyclohexylmethyloxy-2-fluorophenyl)thiazol-2-ylcarbamoyl]-2,6-difluorophenyl}-2-methylacrylic acid (B2074)

1H-NMR(DMSO-d6) 13.0(bs, 2H), 7.98(s, 1H), 7.95(s, 1H), 7.59-7.66(m, 2H), 7.34(s, 1H), 7.12-7.24(m, 2H), 3.90(d, 2H, J=5.7 Hz), 1.61-1.89(m, 9H), 1.03-1.55(m, 5H).

Example 564
Synthesis of (E)-3-{2,6-dichloro-4-[4-(3-cyclohexylmethyloxy-2-fluorophenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methylacrylic acid (B2075)

1H-NMR(DMSO-d6) 13.0(bs, 2H), 8.29(s, 2H), 7.59-7.66(m, 2H), 7.41(s, 1H), 7.12-7.24(m, 2H), 3.90(d, 2H, J=6.0 Hz), 1.62-1.88(m, 9H), 1.02-1.37(m, 5H).

Example 565
Synthesis of (Z)-3-{4-[4-(3-cyclohexylmethyloxy-2-fluorophenyl)thiazol-2-ylcarbamoyl]-2,6-difluorophenyl}-2-methyloxyacrylic acid (B2076)

1H-NMR(DMSO-d6) 13.0(bs, 2H), 7.93(s, 1H), 7.90(s, 1H), 7.60-7.67(m, 2H), 7.12-7.25(m, 2H), 6.66(s, 1H), 3.90(d, 2H, J=5.4 Hz), 3.71(s, 3H), 1.62-1.89(m, 6H), 1.02-1.37(m, 5H).

Example 566
Synthesis of (Z)-3-{2,6-dichloro-4-[4-(3-cyclohexylmethyloxy-2-fluorophenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methyloxyacrylic acid (B2077)

1H-NMR(DMSO-d6) 13.0(bs, 2H), 8.25(s, 2H), 7.59-7.66(m, 2H), 7.13-7.24(m, 2H), 6.73(s, 1H), 3.90(d, 2H, J=5.7 Hz), 3.61(s, 3H), 1.62-1.89(m, 6H), 1.03-1.35(m, 5H).

Example 567
Synthesis of (E)-3-{2,6-difluoro-4-[4-(3-isobutyloxymethyl-2-methyloxyphenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methylacrylic acid (B2078)

1H NMR(DMSO-d6) 13.01(bs, 2H), 7.95-7.99(m, 3H), 7.74(s, 1H), 7.38-7.41(m, 1H), 7.34(s, 1H), 7.25(t, 1H, J=7.5 Hz), 4.57(s, 2H), 3.66(s, 3H), 3.29(d, 2H, J=6.9 Hz), 1.81-1.91(m, 1H), 1.81(s, 3H), 0.91(d, 6H, J=6.6 Hz).

Example 568
Synthesis of (E)-3-{2,6-difluoro-4-[4-(3-isobutyloxymethyl-2-methyloxyphenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methyloxyacrylic acid (B2079)

1H NMR(DMSO-d6) 12.92(bs, 2H), 7.90-7.99(m, 3H), 7.74(s, 1H), 7.39(d, 1H, J=7.5 Hz), 7.25(t, 1H, J=7.5 Hz), 6.65(s, 1H), 4.57(s, 2H), 3.72(s, 3H), 3.65(s, 3H), 3.29(d, 2H, J=6.6 Hz), 1.83-1.91(m, 1H), 0.91(d, 6H, J=6.6 Hz).

Example 569
Synthesis of (E)-3-{2,6-dichloro-4-[4-(3-isobutyloxymethyl-2-methyloxyphenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methylacrylic acid (B2080)

1H NMR(DMSO-d6) 12.99(bs, 2H), 8.29(s, 2H), 7.96-7.99(m, 1H), 7.74(s, 1H), 7.38-7.41(m, 2H), 7.25(t, 1H, J=7.5 Hz), 4.57(s, 2H), 3.66(s, 3H), 3.29(d, 2H, J=6.6 Hz), 1.83-1.92(m, 1H), 1.69(s, 3H), 0.91(d, 6H, J=6.6 Hz).

Example 570
Synthesis of (Z)-3-{2,6-dichloro-4-[4-(3-isobutyloxymethyl-2-methyloxyphenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methyloxyacrylic acid (B2081)

1H NMR(DMSO-d6) 12.97(bs, 2H), 8.25(s, 2H), 7.97(dd, 1H, J=1.5 Hz, 7.8 Hz), 7.74(s, 1H), 7.39(dd, 1H, J=1.5 Hz, 7.5 Hz), 7.25(t, 1H, J=7.8 Hz), 6.72(s, 1H), 4.57(s, 2H), 3.66(s, 3H), 3.62(s, 3H), 3.29(d, 2H, J=6.6 Hz), 1.83-1.92(m, 1H), 0.91(d, 6H, J=6.6 Hz).

Example 571
Synthesis of (E)-3-{4-[4-(3-cyclohexylmethyloxymethyl-2-methyloxyphenyl)thiazol-2-ylcarbamoyl]-2,6-difluorophenyl}-2-methylacrylic acid (B2082)

1H NMR(DMSO-d6) 12.93(bs, 2H), 7.95-7.99(m, 3H), 7.74(s, 1H), 7.39(dd, 1H, J=1.8 Hz, 7.5 Hz), 7.34(s, 1H), 7.24(t, 1H, J=7.5 Hz), 4.57(s, 2H), 3.66(s, 3H), 3.39(d, 2H, J=6.9 Hz), 2.12-2.21(m, 1H), 1.81(s, 3H), 1.65-1.73(m, 2H), 1.47-1.58(m, 4H), 1.21-1.27(m, 2H).

Example 572
Synthesis of (Z)-3-{4-[4-(3-cyclohexylmethyloxymethyl-2-methyloxyphenyl)thiazol-2-ylcarbamoyl]-2,6-difluorophenyl}-2-methyloxyacrylic acid (B2083)

1H NMR(DMSO-d6) 12.93(bs, 2H), 7.90-7.99(m, 3H), 7.74(s, 1H), 7.39(dd, 1H, J=1.8 Hz, 7.5 Hz), 7.24(t, 1H, J=7.5 Hz), 6.65(s, 1H), 4.57(s, 2H), 3.72(s, 3H), 3.66(s, 3H), 3.39(d, 2H, J=6.9 Hz), 2.11-2.21(m, 1H), 1.66-1.73(m, 2H), 1.47-1.58(m, 4H), 1.23-1.30(m, 2H).

Example 573
Synthesis of (E)-3-{2,6-dichloro-4-[4-(3-cyclopentylmethyloxymethyl-2-methyloxyphenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methylacrylic acid (B 2084)

1H NMR(DMSO-d6) 12.99(bs, 2H), 8.29(s, 2H), 7.97(dd, 1H, J=1.8 Hz, 7.8 Hz), 7.73(s, 1H), 7.38-7.41(m, 2H), 7.24(t, 1H, J=7.5 Hz), 4.57(s, 2H), 3.66(s, 3H), 3.39(d, 2H, J=7.2 Hz), 2.11-2.19(m, 1H), 1.69(s, 3H), 1.65-1.73(m, 2H), 1.49-1.58(m, 4H), 1.21-1.27(m, 2H).

Example 574
Synthesis of (Z)-3-{2,6-dichloro-4-[4-(3-cyclopentylmethyloxymethyl-2-methylphenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methyloxyacrylic acid (B2085)

1H NMR(DMSO-d6) 12.95(bs, 2H), 8.25(s, 2H), 7.97(dd, 1H, J=1.8 Hz, 7.8 Hz), 7.73(s, 1H), 7.39(dd, 1H, J=1.8 Hz, 7.5 Hz), 7.24(t, 1H, J=7.8 Hz), 6.73(s, 1H), 4.57(s, 2H), 3.66(s, 3H), 3.62(s, 3H), 3.39(d, 2H, J=7.2 Hz), 2.11-2.21(m, 1H), 1.65-1.71(m, 2H), 1.51-1.58(m, 4H), 1.21-1.27(m, 2H).

Example 575
Synthesis of (E)-3-{2,6-difluoro-4-[4-(2-fluoro-3-isobutyloxyphenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methylacrylic acid (B 2086)

1H NMR(DMSO-d6) 12.85(bs, 2H), 7.79(d, 2H, J=8.4 Hz), 7.43-7.48(m, 2H), 7.16(s, 1H), 6.96-7.07(m, 2H), 3.70(d, 2H, J=6.6 Hz), 1.86-1.92(m, 1H), 1.63(s, 3H), 0.84(d, 6H, J=6.6 Hz).

Example 576
Synthesis of (E)-3-{2,6-dichloro-4-[4-(2-fluoro-3-isobutyloxyphenyl)thiazol-2-ylcarbamoyl}phenyl)-2-methylacrylic acid (B 2087)

1H NMR(DMSO-d6) 12.77(bs, 2H), 8.11(s, 2H), 7.43-7.48(m, 2H), 7.23(d, 1H, J=1.2 Hz), 6.98-7.07(m, 2H), 3.70(d, 2H, J=6.3 Hz), 1.86-1.95(m, 1H), 1.52(s, 3H), 0.84(d, 6H, J=6.6 Hz).

Example 577
Synthesis of (E)-3-{2,6-difluoro-4-[4-(2-fluoro-3-(2-methylbutyloxyphenyl)thiazol-2-ylcarbamoyl)phenyl]-2-methylacrylic acid (B2088)

1H NMR(DMSO-d6) 12.84(bs, 2H), 7.79(d, 2H, J=8.4 Hz), 7.43-7.48(m, 2H), 7.16(s, 1H), 6.97-7.07(m, 2H), 3.68-3.81(m, 2H), 1.68-1.73(m, 1H), 1.64(s, 3H), 1.34-1.41(m, 1H), 1.05-1.14(m, 1H), 0.83(d, 3H, J=6.6 Hz), 0.76(t, 3H, J=7.5 Hz).

Example 578
(E)-3-{4-[6-(3,3-dimethylbutyn-1yl)-4,5-dihydronaphtho[1,2-d]thiazol-2-ylcarbamoyl]-2,6-difluorophenyl}-2-methylacrylic acid (B2089)

1H-NMR(DMSO-d6) 12.87 (bs, 2H), 7.93-7.96 (m, 2H), 7.69-7.72 (m, 1H), 7.32 (s 1H), 7.22-7.29 (m, 2H), 3.13-3.18 (m, 2H), 2.99-3.04 (m, 2H), 1.33 (s, 9H).

Example 579
Synthesis of (Z)-3-(2,6-difluoro-4-{4-[2-methyloxy-3-(2-propyloxyethyl)phenyl]thiazol-2-ylcarbamoyl}phenyl)-2-methyloxyacrylic acid (B2090)

1H-NMR(DMSO-d6) 13.57 (bs, 1H), 12.93 (bs, 1H), 7.86-7.92 (m, 3H), 7.72 (s, 1H), 7.27-7.30 (m, 1H), 7.14-7.19 (m, 1H), 6.66 (s, 1H), 3.71 (s, 3H), 3.60-3.65 (m, 5H), 3.70 (t, 2H, J=6.6 Hz), 2.91 (t, 2H, J=6.9Hz), 1.47-1.54 (m, 2H), 0.85 (t, 3H, J=7.5 Hz).

Example 580
Synthesis of (E)-3-{2,6-dichloro-4-[4-(2-fluoro-3-(3-methylbutyloxyphenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methylacrylic acid (B2097)

1H-NMR(DMSO-d6) 13.0(bs, 2H), 8.29(s, 2H), 7.59-7.66(m, 2H), 7.40(s, 1H), 7.15-7.25(m, 2H), 4.11(t, 2H, J=6.6 Hz), 1.76-1.87(m, 1H), 1.63-1.72(m, 5H), 0.96(d, 6H, J=6.6 Hz).

Example 581
Synthesis of (E)-3-{2,6-dichloro-4-[4-(2-fluoro-3-(2-methylbutyloxyphenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methylacrylic acid (B2098)

1H NMR(DMSO-d6) 12.82(bs, 2H), 8.12(s, 2H), 7.43-7.48(m, 2H), 7.23(s, 1H), 6.96-7.07(m, 2H), 3.68-3.81(m, 2H), 1.68-1.70(m, 1H), 1.52(s, 3H), 1.36-1.43(m, 1H), 1.07-1.14(m, 1H), 0.83(d, 3H, J=6.9 Hz), 0.76(t, 3H, J=6.9 Hz).

Example 582
(E)-3-(4-{4-[2-ethyloxy-3-(1-methyloxydecyl)phenyl]thiazol-2-ylcarbamoyl}-2,6-difluorophenyl)-2-methylacrylic acid (B2099)

1H-NMR(DMSO-d6) 13.00(bs, 2H), 7.93-8.00(m, 2H), 7.86(dd, 1H, J=2.1, 7.8 Hz), 7.70(s, 1H), 7.34(s, 1H), 7.31(dd, 3H, J=2.1, 7.5 Hz), 7.25(t, 1H, J=7.5 Hz), 4.53-4.57(m, 1H), 3.66-3.74(m, 2H), 3.15(s, 3H), 1.81(s, 3H), 1.52-1.78(m, 2H), 1.18-1.50(m, 17H), 0.83-0.87(m, 3H).

Example 583
Synthesis of (Z)-3-{2,6-difluoro-4-[4-(2-fluoro-3-methyloxyphenyl)thiazol-2-ylcarbamoyl]phenyl}-2-methyloxyacrylic acid (B2100)

1H-NMR(DMSO-d6) 13.0(bs, 2H), 7.92(s, 1H), 7.90(s, 1H), 7.60-7.67(m, 2H), 7.13-7.28(m, 2H), 6.66(s, 1H), 3.89(s, 3H), 3.71(s, 3H).

The following compounds can be synthesized by similar reaction to above-mentioned method.
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wherein R⁶, R⁷, and R⁸are each independently fluoro, chloro, or methyl;

- R¹is fluoro or methyl;
- R¹is methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tert-butyl, n-pentyl, neopentyl, n-hexyl, isohexyl, 3,3-dimethylbutyl, 1-methyloxyethyl, 1-methyloxypropyl, 1-methyloxy-3-n-propyloxypropyl, 1-methyloxy-3-n-hexyloxypropyl, 1-methyloxybutyl, 1-methyloxy-4-n-pentyloxypropyl, 1-methyloxy-2-methylpropyl, 1-methyloxypentyl, 1-methyloxy-3-methylbutyl, 3-methyloxy-3-methylbutyl, 1-methyloxy-2,2-dimethylpropyl, 1-methyloxyhexyl, 4-methyloxyhexyl, 1-methyloxy-4-methylpentyl, 1-methyloxy-3,3-dimethylbutyl, 1-methyloxyheptyl, 4-methyloxy-4-heptyl, 3-methyloxy-2,4-dimethyl-3-pentyl, 1-methyloxyoctyl, 3-methyloxyoctyl, 1-methyloxynonyl, 1-methyloxydecyl, 3-methyloxydecyl, 1-methyloxyundecyl, 1-methyloxydoecyl, 1-methyloxy-1-cyclohexylmethyl, 1-(4-ethyloxybutyloxy)-1-cyclohexylmethyl, 1-ethyloxyethyl, 1-ethyloxypropyl, 1-ethyloxy-3-n-hexyloxypropyl, 1-(4-ethyloxybutyloxy)propyl, 1-ethyloxybutyl, 1-ethyloxy-4-n-pentyloxybutyl, 1-ethyloxy-2-methylproyl, 1-ethyloxypentyl, 1-ethyloxy-3-methylbutyl, 1-ethyloxy-2,2-dimethylpropyl, 1-ethyloxyhexyl, 1-ethyloxy-3,3-dimethylbutyl, 1-ethyloxyheptyl, 1-ethyloxyoctyl, 1-ethyloxynonyl, 1-ethyloxydecyl, 1-ethyloxyundecyl, 1-ethyloxydodecyl, 1-ethyloxy-1-cyclohexylmethyl, 1-n-propyloxyethyl, 1-n-propyloxypropyl, 3-n-propyloxypropyl, 1-n-propyloxy-3-n-hexyloxypropyl, 1-n-propyloxybutyl, 1-n-propyloxy-4-n-pentyloxybutyl, 1-n-propyloxy-2-methylpropyl, 1-n-propyloxypentyl, 1-n-propyloxy-3-methylbutyl, 1-n-propyloxy-2,2-dimethylpropyl, 1-n-propyloxyhexyl, 1-n-propyloxy-3,3-dimethylbutyl, 1-n-propyloxyheptyl, 1-n-propyloxyoctyl, 1-n-propyloxynonyl, 1-n-propyloxydecyl, 1-n-propyloxyundecyl, 1-n-propyloxydodecyl, 1-n-propyloxy-1-cyclohexylmethyl, 1-isopropyloxyethyl, 1-isopropyloxypropyl, 3-isopropyloxypropyl, 1-isopropyloxy-3-n-hexyloxypropyl, 1-isopropyloxybutyl, 1-iso-propyloxy-4-n-pentyloxybutyl, 1-isopropyloxy-2-methylpropyl, 1-isopropyloxypentyl, 1-isopropyloxy-3-methylbutyl, 1-isopropyloxy-2,2-dimethylpropyl, 1-isopropyloxyhexyl, 1-isopropyloxy-3,3-dimethylbutyl, 1-isopropyloxyheptyl, 1-isopropyloxyoctyl, 1-isopropyloxynonyl, 1-isopropyloxydecyl, 1-isopropyloxyundecyl, 1-isopropyloxydodecyl, 1-isopropyloxy-1-cyclohexylmethyl, 1-n-butyloxyethyl, 1-n-butyloxypropyl, 3-n-butyloxypropyl, 1-n-butyloxybutyl, 1,4-di(n-butyloxy)butyl, 1-n-butyloxy-2-methylpropyl, 1-n-butyloxypentyl, 1-n-butyloxy-3-methylbutyl, 1-n-butyloxy-2,2-dimethylpropyl, 1-n-butyloxyhexyl, 1-n-butyloxy-3,3-dimethylbutyl, 1-n-butyloxyheptyl, 1-n-butyloxyoctyl, 1-n-butylxynonyl, 1-n-butyloxydecyl, 1-n-butyloxyundecyl, 1-n-butyloxydodecyl, 1-n-butyloxy-1-cyclohexylmethyl, 1-isobutyloxyethyl, 1-isobutyloxypropyl, 1-isobutyloxybutyl, 1-isobutyloxy-2-methylpropyl, 1-isobutyloxypentyl, 1-isobutyloxy-3-methylbutyl, 1-isobutyloxy-2,2-dimethylpropyl, 1-isobutyloxyhexyl, 1-isobutyloxy-3,3-dimethylbutyl, 1-isobutyloxyheptyl, 1-isobutyloxyoctyl, 1-isobutylxynonyl, 1-isobutyloxydecyl, 1-isobutyloxyundecyl, 1-isobutyloxydodecyl, 1-isobutyloxy-1-cyclohexylmethyl, 1-t-butyloxyethyl, 1-t-butyloxypropyl, 1-t-butyloxybutyl, 1-t-butyloxy-2-methylpropyl, 1-t-butyloxypentyl, 1-t-butyloxy-3-methylbutyl, 1-t-butyloxy-2,2-dimethylpropyl, 1-t-butyloxyhexyl, 1-t-butyloxy-3,3-dimethylbutyl, 1-t-butyloxyheptyl, 1-t-butyloxyoctyl, 1-t-butyloxynonyl, 1-t-butyloxydecyl, 1-t-butyloxyundecyl, 1-t-butyloxydodecyl, 1-t-butyloxy-1-cyclohexylmethyl, n-pentyloxymethyl, 1-n-pentyloxyethyl, 1-n-pentyloxypropyl, 3-n-pentyloxypropyl, 1-n-pentyloxy-3-methylthiopropyl, 1-n-pentyloxybutyl, 1-n-pentyloxy-2-methylpropyl, 1-n-pentyloxypentyl, 1-n-pentyloxy-3-methylbutyl, 1-n-p entyloxy-2,2-dimethylpropyl, 1-n-pentyloxyhexyl, 1-n-pentyloxy-3,3-dimethylbutyl, 1-n-pentyloxyheptyl, 1-n-pentyloxyoctyl, 1-n-pentyloxynonyl, 1-n-pentyloxydecyl, 1-n-pentyloxyundecyl, 1-n-pentyloxydodecyl, 1-n-pentyloxy-1-cyclohexylmethyl, 1-neopentyloxyethyl, 1-neopentyloxypropyl, 3-neopentyloxypropyl, 1-neopentyloxy-3-methylthiopropyl, 1-neopentyloxybutyl, 1-neopentyloxy-2-methylpropyl, 1-neopentyloxypentyl, 1-neopentyloxy-3-methylbutyl, 1-neopentyloxy-2,2-dimethylpropyl, 1-neopentyloxyhexyl, 1-neopentyloxy-3,3-dimethylbutyl, 1-neopentyloxyheptyl, 1-neopentyloxyoctyl, 1-neopentyloxynonyl, 1-neopentyloxydecyl, 1-neopentyloxyundecyl, 1-neopentyloxydodecyl, 1-neopentyloxy-1-cyclohexylmethyl, 1-n-hexyloxyethyl, 1-n-hexyloxypropyl, 3-n-hexyloxypropyl, 1-n-hexyloxy-3-methylthiopropyl, 1-n-hexyloxybutyl, 1-n-hexyloxy-2-methylpropyl, 1-n-hexyloxypentyl, 1-n-hexyloxy-3-methylbutyl, 1-n-hexyloxy-2,2-dimethylpropyl, 1-n-hexyloxyhexyl, 1-n-hexyloxy-3,3-dimethylbutyl, 1-n-hexyloxyheptyl, 1-n-hexyloxyoctyl, 1-n-hexyloxynonyl, 1-n-hexyloxydecyl, 1-n-hexylloxyundecyl, 1-n-hexyloxydodecyl, 1-n-hexyloxy-1-cyclohexylmethyl, 3-isohexyloxypropyl, 3-(2-ethylbutyloxy)propyl, 3-(3,3-dimethylbutyloxy)propyl, 3-(2-cyclopentylethyloxy)propyl, 1-n-octyloxyethyl, or n-dodecyloxymethyl

(Compound No., R⁶, R⁷, R⁸, R¹, R²)=(B102, F, F, Me, F, methyl), (B103, F, F, Me, F, ethyl), (B104, F, F, Me, F, n-propyl), (B105, F, F, Me, F, isopropyl), (B106, F, F, Me, F, n-butyl), (B107, F, F, Me, F, isobutyl), (B108, F, F, Me, F, t-butyl), (B109, F, F, Me, F, neopentyl), (B110, F, F, Me, F, n-hexyl), (B111, F, F, OMe, F, methyl), (B112, F, F, OMe, F, ethyl), (B113, F, F, OMe, F, n-propyl), (B114, F, F, OMe, F, isopropyl), (B 115, F, F, OMe, F, n-butyl), (B116, F, F, OMe, F, isobutyl), (B117, F, F, OMe, F, t-butyl), (B118, F, F, OMe, F, n-pentyl), (B119, F, F, OMe, F, neopentyl), (B120, F, F, OMe, F, n-hexyl), (B123, F, F, Me, OMe, methyl), (B124, F, F, Me, OMe, ethyl), (B125, F, F, Me, OMe, n-propyl), (B 126, F, F, Me, OMe, isopropyl), (B 127, F, F, Me, OMe, n-butyl), (B 128, F, F, Me, OMe, isobutyl), (B129, F, F, Me, OMe, t-butyl), (B130, F, F, Me, OMe, n-pentyl), (B131, F, F, Me, OMe, neopentyl), (B132, F, F, Me, OMe, n-hexyl), (B133, F, F, Me, OMe, isohexyl), (B135, F, F, OMe, OMe, methyl), (B136, F, F, OMe, OMe, ethyl), (B137, F, F, OMe, OMe, n-propyl), (B138, F, F, OMe, OMe, isopropyl), (B139, F, F, OMe, OMe, n-butyl), (B140, F, F, OMe, OMe, isobutyl), (B141, F, F, OMe, OMe, t-butyl), (B142, F, F, OMe, OMe, n-pentyl), (B 143, F, F, OMe, OMe, neopentyl), (B 144, F, F, OMe, OMe, n-hexyl), (B145, F, F, OMe, OMe, isohexyl), (B146, F, F, OMe, OMe, 3,3-dimethylbutyl), (B147, Cl, Cl, Me, F, methyl), (B148, Cl, Cl, Me, F, ethyl), (B149, Cl, Cl, Me, F, n-propyl), (B150, Cl, Cl, Me, F, isopropyl), (B151, Cl, Cl, Me, F, n-butyl), (B152, Cl, Cl, Me, F, isobutyl), (B153, Cl, Cl, Me, F, t-butyl), (B154, Cl, Cl, Me, F, n-pentyl), (B155, Cl, Cl, Me, F, neopentyl), (B156, Cl, Cl, Me, F, n-hexyl), (B157, Cl, Cl, Me, F, isohexyl), (B158, Cl, Cl, Me, F, 3,3-dimethylbutyl), (B159, Cl, Cl, OMe, F, methyl), (B160, Cl, Cl, OMe, F, ethyl), (B161, Cl, Cl, OMe, F, n-propyl), (B162, Cl, Cl, OMe, F, isopropyl), (B163, Cl, Cl, OMe, F, n-butyl), (B164, Cl, Cl, OMe, F, isobutyl), (B165, Cl, Cl, OMe, F, t-butyl), (B166, Cl, Cl, OMe, F, n-pentyl), (B167, Cl, Cl, OMe, F, neopentyl), (B168, Cl, Cl, OMe, F, n-hexyl), (B171, Cl, Cl, Me, OMe, methyl), (B172, Cl, Cl, Me, OMe, ethyl), (B173, Cl, Cl, Me, OMe, n-propyl), (B174, Cl, Cl, Me, OMe, isopropyl), (B175, Cl, Cl, Me, OMe, n-butyl), (B176, Cl, Cl, Me, OMe, isobutyl), (B177, Cl, Cl, Me, OMe, t-butyl), (B178, Cl, Cl, Me, OMe, n-pentyl), (B179, Cl, Cl, Me, OMe, neopentyl), (B180, Cl, Cl, Me, OMe, n-hexyl), (B181, Cl, Cl, Me, OMe, isohexyl), (B182, Cl, Cl, Me, OMe, 3,3-dimethylbutyl), (B183, Cl, Cl, OMe, OMe, methyl), (B184, Cl, Cl, OMe, OMe, ethyl), (B185, Cl, Cl, OMe, OMe, n-propyl), (B186, Cl, Cl, OMe, OMe, isopropyl), (B187, Cl, Cl, OMe, OMe, n-butyl), (B188, Cl, Cl, OMe, OMe, isobutyl), (B189, Cl, Cl, OMe, OMe, t-butyl), (B190, Cl, Cl, OMe, OMe, n-pentyl), (B191, Cl, Cl, OMe, OMe, neopentyl), (B192, Cl, Cl, OMe, OMe, n-hexyl), (B193, Cl, Cl, OMe, OMe, isohexyl), (B194, Cl, Cl, OMe, OMe, 3,3-dimethylbutyl), (B196, F, F, Me, F, 1-methyloxypropyl), (B197, F, F, Me, F, 1-methyloxybutyl), (B198, F, F, Me, F, 1-methyloxy-2-methylpropyl), (B199, F, F, Me, F, 1-methyloxypentyl), (B200, F, F, Me, F, 1-methyloxy-3-methylbutyl), (B201, F, F, Me, F, 3-methyloxyoctyl), (B202, F, F, Me, F, 1-ethyloxyethyl), (B203, F, F, Me, F, 1-ethyloxy-3-n-hexyloxypropyl), (B204, F, F, Me, F, 1-ethyloxy-4-n-pentyloxybutyl), (B205, F, F, Me, F, 1-ethyloxybutyl), (B206, F, F, Me, F, 1-ethyloxy-2-methylpropyl), (B207, F, F, Me, F, 1-ethyloxy-3-methylbutyl), (B208, F, F, Me, F, 1-ethyloxyhexyl), (B209, F, F, Me, F, 1-ethyloxy-3,3-dimethylbutyl), (B210, F, F, Me, F, 1-ethyloxyheptyl), (B211, F, F, Me, F, 1-ethyloxyoctyl), (B212, F, F, Me, F, 1-ethyloxynonyl), (B213, F, F, Me, F, 1-ethyloxydecyl), (B214, F, F, Me, F, 1-ethyloxyundecyl), (B215, F, F, Me, F, 1-ethyloxydodecyl), (B217, F, F, Me, F, 1-n-propyloxypropyl), (B218, F, F, Me, F, 3-n-propyloxypropyl), (B219, F, F, Me, F, 1-n-propyloxy-3-n-hexyloxypropyl), (B220, F, F, Me, F, 1-n-propyloxy-4-n-pentyloxybutyl), (B221, F, F, Me, F, 1,4-di(n-propyloxy)butyl), (B222, F, F, Me, F, 1-n-propyloxy-2-methylpropyl), (B223, F, F, Me, F, 1-n-propyloxy-3-methylbutyl), (B224, F, F, Me, F, 1-n-propyloxy-2,2-dimethylpropyl), (B225, F, F, Me, F, 1-n-propyloxyhexyl), (B226, F, F, Me, F, 1-n-propyloxy-3,3-dimethylbutyl), (B227, F, F, Me, F, 1-n-propyloxyheptyl), (B228, F, F, Me, F, 1-n-propyloxyoctyl), (B229, F, F, Me, F, 1-n-propyloxynonyl), (B230, F, F, Me, F, 1-n-propyloxydecyl), (B231, F, F, Me, F, 1-n-propyloxyundecyl), (B232, F, F, Me, F, 1-n-propyloxydodecyl), (B234, F, F, Me, F, 1-isopropyloxyethyl), (B235, F, F, Me, F, 1-isopropyloxypropyl), (B236, F, F, Me, F, 3-isopropyloxypropyl), (B237, F, F, Me, F, 1-isopropyloxy-3-n-hexyloxypropyl), (B238, F, F, Me, F, 1-isopropyloxybutyl), (B239, F, F, Me, F, 1-isopropyloxy-4-n-pentyloxybutyl), (B240, F, F, Me, F, 1-isopropyloxy-2-methylpropyl), (B241, F, F, Me, F, 1-isopropyloxypentyl), (B242, F, F, Me, F, 1-isopropyloxy-3-methylbutyl), (B243, F, F, Me, F, 1-isopropyloxy-2,2-dimethylpropyl), (B244, F, F, Me, F, 1-isopropyloxyhexyl), (B245, F, F, Me, F, 1-isopropyloxy-3,3-dimethylbutyl), (B246, F, F, Me, F, 1-isopropyloxyheptyl), (B247, F, F, Me, F, 1-isopropyloxyoctyl), (B248, F, F, Me, F, 1-isopropyloxynonyl), (B249, F, F, Me, F, 1-isopropyloxydecyl), (B250, F, F, Me, F, 1-isopropyloxyundecyl), (B251, F, F, Me, F, 1-isopropyloxydodecyl), (B252, F, F, Me, F, 1-isopropyloxy-1-cyclohexylmethyl), (B253, F, F, Me, F, 1-n-butyloxy-2-methylpropyl), (B254, F, F, Me, F, 1-n-butyloxy-3-methylbutyl), (B256, F, F, Me, F, 1-n-butyloxyhexyl), (B257, F, F, Me, F, 1-n-butyloxy-3,3-dimethylbutyl), (B258, F, F, Me, F, 1-n-butyloxyheptyl), (B259, F, F, Me, F, 1-n-butyloxyoctyl), (B260, F, F, Me, F, 1-n-butyloxynonyl), (B261, F, F, Me, F, 1-n-butyloxydecyl), (B262, F, F, Me, F, 1-n-butyloxyundecyl), (B263, F, F, Me, F, 1-n-butyloxydodecyl), (B265, F, F, Me, F, 1-isobutyloxyethyl), (B266, F, F, Me, F, 1-isobutyloxypropyl), (B267, F, F, Me, F, 1-isobutyloxybutyl), (B268, F, F, Me, F, 1-isobutyloxy-2-methylpropyl), (B269, F, F, Me, F, 1-isobutyloxypentyl), (B270, F, F, Me, F, 1-isobutyloxy-3-methylbutyl), (B271, F, F, Me, F, 1-isobutyloxy-2,2-dimethylpropyl), (B272, F, F, Me, F, 1-isobutyloxyhexyl), (B273, F, F, Me, F, 1-isobutyloxy-3,3-dimethylbutyl), (B274, F, F, Me, F, 1-isobutyloxyheptyl), (B275, F, F, Me, F, 1-isobutyloxyoctyl), (B276, F, F, Me, F, 1-isobutyloxyynonyl), (B277, F, F, Me, F, 1-isobutyloxydecyl), (B278, F, F, Me, F, 1-isobutyloxyundecyl), (B279, F, F, Me, F, 1-isobutyloxydodecyl), (B280, F, F, Me, F, 1-isobutyloxy-1-cyclohexylmethyl), (B281, F, F, Me, F, 1-t-butyloxyethyl), (B282, F, F, Me, F, 1-t-butyloxypropyl), (B283, F, F, Me, F, 1-t-butyloxybutyl), (B284, F, F, Me, F, 1-t-butyloxy-2-methylpropyl), (B285, F, F, Me, F, 1-t-butyloxypentyl), (B286, F, F, Me, F, 1-t-butyloxy-3-methylbutyl), (B287, F, F, Me, F, 1-t-butyloxy-2,2-dimethylpropyl), (B288, F, F, Me, F, 1-t-butyloxyhexyl), (B289, F, F, Me, F, 1-t-butyloxy-3,3-dimethylbutyl), (B290, F, F, Me, F, 1-t-butyloxyheptyl), (B291, F, F, Me, F, 1-t-butyloxyoctyl), (B292, F, F, Me, F, 1-t-butyloxynonyl), (B293, F, F, Me, F, 1-t-butyloxydecyl), (B294, F, F, Me, F, 1-t-butyloxyundecyl), (B295, F, F, Me, F, 1-t-butyloxyydodecyl), (B296, F, F, Me, F, 1-t-butyloxy-1-cyclohexylmethyl), (B297, F, F, Me, F, 1-n-pentyloxy-2-methylpropyl), (B298, F, F, Me, F, 1-n-pentyloxy-3-methylbutyl), (B299, F, F, Me, F, 1-n-pentyloxyhexyl), (B300, F, F, Me, F, 1-n-pentyloxy-3,3-dimethylbutyl), (B301, F, F, Me, F, 1-n-pentyloxyheptyl), (B302, F, F, Me, F, 1-n-pentyloxyoctyl), (B303, F, F, Me, F, 1-n-pentyloxynonyl), (B304, F, F, Me, F, 1-n-pentyloxydecyl), (B305, F, F, Me, F, 1-n-pentyloxyundecyl), (B306, F, F, Me, F, 1-n-pentyloxydodecyl), (B307, F, F, Me, F, 1-neopentyloxyethyl), (B308, F, F, Me, F, 1-neopentyloxypropyl), (B309, F, F, Me, F, 1-neopentyloxybutyl), (B310, F, F, Me, F, 1-neopentyloxy-2-methylpropyl), (B311, F, F, Me, F, 1-neopentyloxypentyl), (B312, F, F, Me, F, 1-neopentyloxy-3-methylbutyl), (B313, F, F, Me, F, 1-neopentyloxy-2,2-dimethylpropyl), (B314, F, F, Me, F, 1-neopentyloxyhexyl), (B315, F, F, Me, F, 1-neopentyloxy-3,3-dimethylbutyl), (B316, F, F, Me, F, 1-neopentyloxyheptyl), (B317, F, F, Me, F, 1-neopentyloxyoctyl), (B318, F, F, Me, F, 1-neopentyloxynonyl), (B319, F, F, Me, F, 1-neopentyloxydecyl), (B320, F, F, Me, F, 1-neopentyloxyundecyl), (B321, F, F, Me, F, 1-neopentyloxydodecyl), (B322, F, F, Me, F, 1-neopentyloxy-1-cyclohexylmethyl), (B323, F, F, Me, F, 1-n-hexyloxyethyl), (B324, F, F, Me, F, 1-n-hexyloxybutyl), (B325, F, F, Me, F, 1-n-hexyloxy-2-methylpropyl), (B326, F, F, Me, F, 1-n-hexyloxypentyl), (B327, F, F, Me, F, 1-n-hexyloxy-3-methylbutyl), (B328, F, F, Me, F, 1-n-hexyloxy-2,2-dimethylpropyl), (B329, F, F, Me, F, 1-n-hexyloxyhexyl), (B330, F, F, Me, F, 1-n-hexyloxy-3,3-dimethylbutyl), (B331, F, F, Me, F, 1-n-hexyloxyheptyl), (B332, F, F, Me, F, 1-n-hexyloxyoctyl), (B333, F, F, Me, F, 1-n-hexyloxynonyl), (B334, F, F, Me, F, 1-n-hexyloxydecyl), (B335, F, F, Me, F, 1-n-hexyloxyundecyl), (B336, F, F, Me, F, 1-n-hexyloxydodecyl), (B337, F, F, Me, F, 1-n-hexyloxy-1-cyclohexylmethyl), (B338, F, F, Me, OMe, 1-methyloxyethyl), (B339, F, F, Me, OMe, 1-methyloxypropyl), (B340, F, F, Me, OMe, 1-methyloxy-3-n-hexyloxypropyl), (B341, F, F, Me, OMe, 1-methyloxybutyl), (B342, F, F, Me, OMe, 1-methyloxy-4-n-pentyloxybutyl), (B343, F, F, Me, OMe, 1-methyloxy-2-methylpropyl), (B344, F, F, Me, OMe, 1-methyloxypentyl), (B345, F, F, Me, OMe, 1-methyloxy-3-methylbutyl), (B346, F, F, Me, OMe, 1-methyloxy-2,2-dimethylpropyl), (B350, F, F, Me, OMe, 1-methyloxyheptyl), (B351, F, F, Me, OMe, 1-methyloxyoctyl), (B352, F, F, Me, OMe, 3-methyloxyoctyl), (B353, F, F, Me, OMe, 1-methyloxynonyl), (B356, F, F, Me, OMe, 1-methyloxydodecyl), (B357, F, F, Me, OMe, 1-methyloxy-1-cyclohexylmethyl), (B358, F, F, Me, OMe, 1-(4-ethyloxybutyloxy)-1-cyclohexylmethyl), (B359, F, F, Me, OMe, 1-ethyloxyethyl), (B360, F, F, Me, OMe, 1-(4-ethyloxybutyloxy)propyl), (B361, F, F, Me, OMe, 1-ethyloxypropyl), (B362, F, F, Me, OMe, 1-ethyloxy-3-n-hexyloxypropyl), (B363, F, F, Me, OMe, 1-ethyloxybutyl), (B364, F, F, Me, OMe, 1-ethyloxy-3-n-pentylbutyl), (B365, F, F, Me, OMe, 1-ethyloxy-2-methylpropyl), (B366, F, F, Me, OMe, 1-ethyloxypentyl), (B367, F, F, Me, OMe, 1-ethyloxy-3-methylbutyl), (B368, F, F, Me, OMe, 1-ethyloxy-2,2-dimethylpropyl), (B369, F, F, Me, OMe, 1-ethyloxyhexyl), (B370, F, F, Me, OMe, 1-ethyloxy-3,3-dimethylbutyl), (B371, F, F, Me, OMe, 1-ethyloxyheptyl), (B372, F, F, Me, OMe, 1-ethyloxyoctyl), (B 373, F, F, Me, OMe, 1-ethyloxynonyl), (B374, F, F, Me, OMe, 1-ethyloxydecyl), (B375, F, F, Me, OMe, 1-ethyloxyundecyl), (B376, F, F, Me, OMe, 1-ethyloxydodecyl), (B377, F, F, Me, OMe, 1-ethyloxy-1-cyclohexylmethyl), (B378, F, F, Me, OMe, 1-n-propyloxyethyl), (B379, F, F, Me, OMe, 1-n-propyloxypropyl), (B381, F, F, Me, OMe, 1-n-propyloxy-3-n-hexyloxypropyl), (B382, F, F, Me, OMe, 1-n-propyloxybutyl), (B383, F, F, Me, OMe, 1-n-propyloxy-4-n-pentyloxybutyl), (B384, F, F, Me, OMe, 1,4-di(n-propyloxy)butyl), (B385, F, F, Me, OMe, 1-n-propyloxy-2-methylpropyl), (B386, F, F, Me, OMe, 1-n-propyloxypentyl), (B387, F, F, Me, OMe, 1-n-propyloxy-3-methylbutyl), (B388, F, F, Me, OMe, 1-n-propyloxy-2,2-dimethylpropyl), (B389, F, F, Me, OMe, 1-n-propyloxyhexyl), (B390, F, F, Me, OMe, 1-n-propyloxy-3,3-dimethylbutyl), (B391, F, F, Me, OMe, 1-n-propyloxyheptyl), (B392, F, F, Me, OMe, 1-n-propyloxyoctyl), (B393, F, F, Me, OMe, 1-n-propyloxynonyl), (B394, F, F, Me, OMe, 1-n-propyloxydecyl), (B395, F, F, Me, OMe, 1-n-propyloxyundecyl), (B396, F, F, Me, OMe, 1-n-propyloxydodecyl), (B398, F, F, Me, OMe, 1-isopropyloxyethyl), (B399, F, F, Me, OMe, 1-isopropyloxypropyl), (B400, F, F, Me, OMe, 3-isopropyloxypropyl), (B401, F, F, Me, OMe, 1-isopropyloxy-3-n-hexyloxypropyl), (B402, F, F, Me, OMe, 1-isopropyloxybutyl), (B403, F, F, Me, OMe, 1-isopropyloxy-4-n-pentyloxybutyl), (B404, F, F, Me, OMe, 1-isopropyloxy-2-methylpropyl), (B405, F, F, Me, OMe, 1-isopropyloxypentyl), (B406, F, F, Me, OMe, 1-isopropyloxy-3-methylbutyl), (B407, F, F, Me, OMe, 1-isopropyloxy-2,2-dimethylpropyl), (B408, F, F, Me, OMe, 1-isopropyloxyhexyl), (B409, F, F, Me, OMe, 1-isopropyloxy-3,3-dimethylbutyl), (B410, F, F, Me, OMe, 1-isopropyloxyheptyl), (B411, F, F, Me, OMe, 1-isopropyloxyoctyl), (B412, F, F, Me, OMe, 1-isopropyloxynonyl), (B413, F, F, Me, OMe, 1-isopropyloxydecyl), (B414, F, F, Me, OMe, 1-isopropyloxyundecyl), (B415, F, F, Me, OMe, 1-isopropyloxydodecyl), (B416, F, F, Me, OMe, 1-isopropyloxy-1-cyclohexylmethyl), (B417, F, F, Me, OMe, 1-n-butyloxyethyl), (B420, F, F, Me, OMe, 1-n-butyloxybutyl), (B421, F, F, Me, OMe, 1,4-di(n-butyloxy)butyl), (B422, F, F, Me, OMe, 1-n-butyloxy-2-methylpropyl), (B423, F, F, Me, OMe, 1-n-butyloxypentyl), (B424, F, F, Me, OMe, 1-n-butyloxy-3-methylbutyl), (B426, F, F, Me, OMe, 1-n-butyloxyhexyl), (B427, F, F, Me, OMe, 1-n-butyloxy-3,3-dimethylbutyl), (B428, F, F, Me, OMe, 1-n-butyloxyheptyl), (B429, F, F, Me, OMe, 1-n-butyloxyoctyl), (B430, F, F, Me, OMe, 1-n-butyloxynonyl), (B431, F, F, Me, OMe, 1-n-butyloxydecyl), (B432, F, F, Me, OMe, 1-n-butyloxyundecyl), (B433, F, F, Me, OMe, 1-n-butyloxydodecyl), (B434, F, F, Me, OMe, 1-n-butyloxy-l-cyclohexylmethyl), (B435, F, F, Me, OMe, 1-isobutyloxyethyl), (B436, F, F, Me, OMe, 1-isobutyloxypropyl), (B437, F, F, Me, OMe, 1-isobutyloxybutyl), (B438, F, F, Me, OMe, 1-isobutyloxy-2-methylpropyl), (B439, F, F, Me, OMe, 1-isobutyloxypentyl), (B440, F, F, Me, OMe, 1-isobutyloxy-3-methylbutyl), (B441, F, F, Me, OMe, 1-isobutyloxy-2,2-dimethylpropyl), (B442, F, F, Me, OMe, 1-isobutyloxyhexyl), (B443, F, F, Me, OMe, 1-isobutyloxy-3,3-dimethylbutyl), (B444, F, F, Me, OMe, 1-isobutyloxyheptyl), (B445, F, F, Me, OMe, 1-isobutyloxyoctyl), (B446, F, F, Me, OMe, 1-isobutyloxyynonyl), (B447, F, F, Me, OMe, 1-isobutyloxydecyl), (B448, F, F, Me, OMe, 1-isobutyloxyundecyl), (B449, F, F, Me, OMe, 1-isobutyloxydodecyl), (B450, F, F, Me, OMe, 1-isobutyloxy-1-cyclohexylmethyl), (B451, F, F, Me, OMe, 1-t-butyloxyethyl), (B452, F, F, Me, OMe, 1-t-butyloxypropyl), (B453, F, F, Me, OMe, 1-t-butyloxybutyl), (B454, F, F, Me, OMe, 1-t-butyloxy-2-methylpropyl), (B455, F, F, Me, OMe, 1-t-butyloxypentyl), (B456, F, F, Me, OMe, 1-t-butyloxy-3-methylbutyl), (B457, F, F, Me, OMe, 1-t-butyloxy-2,2-dimethylpropyl), (B458, F, F, Me, OMe, 1-t-butyloxyhexyl), (B459, F, F, Me, OMe, 1-t-butyloxy-3,3-dimethylbutyl), (B460, F, F, Me, OMe, 1-t-butyloxyheptyl), (B461, F, F, Me, OMe, 1-t-butyloxyoctyl), (B462, F, F, Me, OMe, 1-t-butyloxynonyl), (B463, F, F, Me, OMe, 1-t-butyloxydecyl), (B464, F, F, Me, OMe, 1-t-butyloxyundecyl), (B465, F, F, Me, OMe, 1-t-butyloxydodecyl), (B466, F, F, Me, OMe, 1-t-butyloxy-1-cyclohexylmethyl), (B467, F, F, Me, OMe, 1-n-pentyloxyethyl), (B468, F, F, Me, OMe, 1-n-pentyloxypropyl), (B469, F, F, Me, OMe, 3-n-pentyloxypropyl), (B470, F, F, Me, OMe, 1-n-pentyloxy-3-methylthiopropyl), (B471, F, F, Me, OMe, 1-n-pentyloxybutyl), (B472, F, F, Me, OMe, 1-n-pentyloxy-2-methylpropyl), (B473, F, F, Me, OMe, 1-n-pentyloxypentyl), (B474, F, F, Me, OMe, 1-n-pentyloxy-3-methylbutyl), (B475, F, F, Me, OMe, 1-n-pentyloxy-2,2-dimethylpropyl), (B476, F, F, Me, OMe, 1-n-pentyloxyhexyl), (B477, F, F, Me, OMe, 1-n-pentyloxy-3,3-dimethylbutyl), (B478, F, F, Me, OMe, 1-n-pentyloxyheptyl), (B479, F, F, Me, OMe, 1-n-pentyloxyoctyl), (B480, F, F, Me, OMe, 1-n-pentyloxynonyl), (B481, F, F, Me, OMe, 1-n-pentyloxydecyl), (B482, F, F, Me, OMe, 1-n-pentyloxyundecyl), (B483, F, F, Me, OMe, 1-n-pentyloxydodecyl), (B484, F, F, Me, OMe, 1-n-pentyloxyl-cyclohexylmethyl), (B485, F, F, Me, OMe, 1-isopentyloxypropyl), (B486, F, F, Me, OMe, 1-neopentyloxyethyl), (B487, F, F, Me, OMe, 1-neopentyloxypropyl), (B489, F, F, Me, OMe, 1-neopentyloxybutyl), (B490, F, F, Me, OMe, 1-neopentyloxy-2-methylpropyl), (B491, F, F, Me, OMe, 1-neopentyloxypentyl), (B492, F, F, Me, OMe, 1-neopentyloxy-3-methylbutyl), (B493, F, F, Me, OMe, 1-neopentyloxy-2,2-dimethylpropyl), (B494, F, F, Me, OMe, 1-neopentyloxyhexyl), (B495, F, F, Me, OMe, 1-neopentyloxy-3,3-dimethylbutyl), (B496, F, F, Me, OMe, 1-neopentyloxyheptyl), (B497, F, F, Me, OMe, 1-neopentyloxyoctyl), (B498, F, F, Me, OMe, 1-neopentyloxynonyl), (B499, F, F, Me, OMe, 1-neopentyloxydecyl), (B500, F, F, Me, OMe, 1-neopentyloxyundecyl), (B501, F, F, Me, OMe, 1-neopentyloxydodecyl), (B502, F, F, Me, OMe, 1-neopentyloxy-1-cyclohexylmethyl), (B503, F, F, Me, OMe, 1-n-hexyloxyethyl), (B504, F, F, Me, OMe, 1-n-hexyloxypropyl), (B506, F, F, Me, OMe, 1-n-hexyloxybutyl), (B507, F, F, Me, OMe, 1-n-hexyloxy-2-methylpropyl), (B508, F, F, Me, OMe, 1-n-hexyloxypentyl), (B509, F, F, Me, OMe, 1-n-hexyloxy-3-methylbutyl), (B510, F, F, Me, OMe, 1-n-hexyloxy-2,2-dimethylpropyl), (B511, F, F, Me, OMe, 1-n-hexyloxyhexyl), (B512, F, F, Me, OMe, 1-n-hexyloxy-3,3-dimethylbutyl), (B513, F, F, Me, OMe, 1-n-hexyloxyheptyl), (B514, F, F, Me, OMe, 1-n-hexyloxyoctyl), (B515, F, F, Me, OMe, 1-n-hexyloxynonyl), (B516, F, F, Me, OMe, 1-n-hexyloxydecyl), (B517, F, F, Me, OMe, 1-n-hexyloxyundecyl), (B518, F, F, Me, OMe, 1-n-hexyloxydodecyl), (B520, F, F, Me, OMe, 3-isohexyloxydodecyl), (B522, F, F, Me, OMe, 3-(2-cyclopentylethyloxy)propyl), (B523, F, F, Me, OMe, 1-n-octyloxydodecyl), (B524, F, F, OMe, F, 1-methyloxyethyl), (B525, F, F, OMe, F, 1-methyloxypropyl), (B526, F, F, OMe, F, 1-methyloxy-3-n-hexyloxypropyl), (B527, F, F, OMe, F, 1-methyloxybutyl), (B528, F, F, OMe, F, 1-methyloxy-4-n-pentyloxybutyl), (B529, F, F, OMe, F, 1-methyloxy-2-methylpropyl), (B530, F, F, OMe, F, 1-methyloxypentyl), (B531, F, F, OMe, F, 1-methyloxy-3-methylbutyl), (B532, F, F, OMe, F, 1-methyloxy-2,2-dimethylpropyl), (B534, F, F, OMe, F, 4-methyloxyhexyl), (B535, F, F, OMe, F, 1-methyloxy-4-methylpentyl), (B536, F, F, OMe, F, 1-methyloxy-3,3-dimethylbutyl), (B537, F, F, OMe, F, 3-methyloxy-2,4-dimethyl-3-pentyl), (B538, F, F, OMe, F, 1-methyloxyheptyl), (B539, F, F, OMe, F, 4-methyloxy-4-heptyl), (B540, F, F, OMe, F, 1-methyloxyoctyl), (B541, F, F, OMe, F, 3-methyloxyoctyl), (B542, F, F, OMe, F, 1-methyloxynonyl), (B543, F, F, OMe, F, 1-methyloxydecyl), (B544, F, F, OMe, F, 1-methyloxyundecyl), (B545, F, F, OMe, F, 1-methyloxydodecyl), (B546, F, F, OMe, F, 1-methyloxy-1-cyclohexylmethyl), (B547, F, F, OMe, F, 1-(4-ethyloxybutyloxy)-1-cyclohexylmethyl), (B548, F, F, OMe, F, 1-ethyloxyethyl), (B549, F, F, OMe, F, 1-ethyloxypropyl), (B550, F, F, OMe, F, 1-ethyloxy-3-n-hexyloxypropyl), (B551, F, F, OMe, F, 1-(4-ethyloxybutyloxy)propyl), (B552, F, F, OMe, F, 1-ethyloxybutyl), (B553, F, F, OMe, F, 1-ethyloxy-4-n-pentyloxybutyl), (B554, F, F, OMe, F, 1-ethyloxy-2-methylpropyl), (B555, F, F, OMe, F, 1-ethyloxypentyl), (B556, F, F, OMe, F, 1-ethyloxy-3-methylbutyl), (B557, F, F, OMe, F, 1-ethyloxy-2,2-dimethylpropyl), (B558, F, F, OMe, F, 1-ethyloxyhexyl), (B559, F, F, OMe, F, 1-ethyloxy-3,3-dimethylbutyl), (B560, F, F, OMe, F, 1-ethyloxyheptyl), (B561, F, F, OMe, F, 1-ethyloxyoctyl), (B562, F, F, OMe, F, 1-ethyloxynonyl), (B563, F, F, OMe, F, 1-ethyloxydecyl), (B564, F, F, OMe, F, 1-ethyloxyundecyl), (B565, F, F, OMe, F, 1-ethyloxydodecyl), (B566, F, F, OMe, F, 1-ethyloxy-1-cyclohexylmethyl), (B567, F, F, OMe, F, 1-n-propyloxyethyl), (B568, F, F, OMe, F, 1-n-propyloxypropyl), (B569, F, F, OMe, F, 3-n-propyloxypropyl), (B570, F, F, OMe, F, 1-n-propyloxy-3-n-hexyloxypropyl), (B571, F, F, OMe, F, 1-n-propyloxybutyl), (B572, F, F, OMe, F, 1-n-propyloxy-4-n-pentyloxybutyl), (B573, F, F, OMe, F, 1,4-di(n-propyloxy)butyl), (B574, F, F, OMe, F, 1-n-propyloxy-2-methylpropyl), (B575, F, F, OMe, F, 1-n-propyloxypentyl), (B576, F, F, OMe, F, 1-n-propyloxy-3-methylbutyl), (B577, F, F, OMe, F, 1-n-propyloxy-2,2-dimethylpropyl), (B578, F, F, OMe, F, 1-n-propyloxyhexyl), (B579, F, F, OMe, F, 1-n-propyloxy-3,3-dimethylbutyl), (B580, F, F, OMe, F, 1-n-propyloxyheptyl), (B581, F, F, OMe, F, 1-n-propyloxyoctyl), (B582, F, F, OMe, F, 1-n-propyloxynonyl), (B583, F, F, OMe, F, 1-n-propyloxydecyl), (B584, F, F, OMe, F, 1-n-propyloxyundecyl), (B585, F, F, OMe, F, 1-n-propyloxydodecyl), (B586, F, F, OMe, F, 1-n-propyloxy-1-cyclohexylmethyl), (B587, F, F, OMe, F, 1-isopropyloxyethyl), (B588, F, F, OMe, F, 1-isopropyloxypropyl), (B589, F, F, OMe, F, 3-isopropyloxypropyl), (B590, F, F, OMe, F, 1-isopropyloxy-3-n-hexyloxypropyl), (B591, F, F, OMe, F, 1-isopropyloxybutyl), (B592, F, F, OMe, F, 1-isopropyloxy-4-n-pentyloxybutyl), (B593, F, F, OMe, F, 1-isopropyloxy-2-methylpropyl), (B594, F, F, OMe, F, 1-isopropyloxypentyl), (B595, F, F, OMe, F, 1-isopropyloxy-3-methylbutyl), (B596, F, F, OMe, F, 1-isopropyloxy-2,2-dimethylpropyl), (B597, F, F, OMe, F, 1-isopropyloxyhexyl), (B598, F, F, OMe, F, 1-isopropyloxy-3,3-dimethylbutyl), (B599, F, F, OMe, F, 1-isopropyloxyheptyl), (B600, F, F, OMe, F, 1-isopropyloxyoctyl), (B601, F, F, OMe, F, 1-isopropyloxynonyl), (B602, F, F, OMe, F, 1-isopropyloxydecyl), (B603, F, F, OMe, F, 1-isopropyloxyundecyl), (B604, F, F, OMe, F, 1-isopropyloxydodecyl), (B605, F, F, OMe, F, 1-isopropyloxy-1-cyclohexylmethyl), (B606, F, F, OMe, F, 1-n-butyloxyethyl), (B607, F, F, OMe, F, 1-n-butyloxypropyl), (B608, F, F, OMe, F, 3-n-butyloxypropyl), (B609, F, F, OMe, F, 1-n-butyloxybutyl), (B610, F, F, OMe, F, 1,4-di(n-butyloxy)butyl), (B611, F, F, OMe, F, 1-n-butyloxy-2-methylpropyl), (B612, F, F, OMe, F, 1-n-butyloxypentyl), (B613, F, F, OMe, F, 1-n-butyloxy-3-methylbutyl), (B614, F, F, OMe, F, 1-n-butyloxy-2,2-dimethylpropyl), (B615, F, F, OMe, F, 1-n-butyloxyhexyl), (B616, F, F, OMe, F, 1-n-butyloxy-3,3-dimethylbutyl), (B617, F, F, OMe, F, 1-n-butyloxyheptyl), (B618, F, F, OMe, F, 1-n-butyloxyoctyl), (B619, F, F, OMe, F, 1-n-butyloxynonyl), (B620, F, F, OMe, F, 1-n-butyloxydecyl), (B621, F, F, OMe, F, 1-n-butyloxyundecyl), (B622, F, F, OMe, F, 1-n-butyloxydodecyl), (B623, F, F, OMe, F, 1-n-butyloxy-1-cyclohexylmethyl), (B624, F, F, OMe, F, 1-isobutyloxyethyl), (B625, F, F, OMe, F, 1-isobutyloxypropyl), (B626, F, F, OMe, F, 1-isobutyloxybutyl), (B627, F, F, OMe, F, 1-isobutyloxy-2-methylpropyl), (B628, F, F, OMe, F, 1-isobutyloxypentyl), (B629, F, F, OMe, F, 1-isobutyloxy-3-methylbutyl), (B630, F, F, OMe, F, 1-isobutyloxy-2,2-dimethylpropyl), (B631, F, F, OMe, F, 1-isobutyloxyhexyl), (B632, F, F, OMe, F, 1-isobutyloxy-3,3-dimethylbutyl), (B633, F, F, OMe, F, 1-isobutyloxyheptyl), (B634, F, F, OMe, F, 1-isobutyloxyoctyl), (B635, F, F, OMe, F, 1-isobutyloxyynonyl), (B636, F, F, OMe, F, 1-isobutyloxydecyl), (B637, F, F, OMe, F, 1-isobutyloxyundecyl), (B638, F, F, OMe, F, 1-isobutyloxydodecyl), (B639, F, F, OMe, F, 1-isobutyloxy-1-cyclohexylmethyl), (B640, F, F, OMe, F, 1-t-butyloxyethyl), (B641, F, F, OMe, F, 1-t-butyloxypropyl), (B642, F, F, OMe, F, 1-t-butyloxybutyl), (B643, F, F, OMe, F, 1-t-butyloxy-2-methylpropyl), (B644, F, F, OMe, F, 1-t-butyloxypentyl), (B645, F, F, OMe, F, 1-t-butyloxy-3-methylbutyl), (B646, F, F, OMe, F, 1-t-butyloxy-2,2-dimethylpropyl), (B647, F, F, OMe, F, 1-t-butyloxyhexyl), (B648, F, F, OMe, F, 1-t-butyloxy-3,3-dimethylbutyl), (B649, F, F, OMe, F, 1-t-butyloxyheptyl), (B650, F, F, OMe, F, 1-t-butyloxyoctyl), (B651, F, F, OMe, F, 1-t-butyloxynonyl), (B652, F, F, OMe, F, 1-t-butyloxydecyl), (B653, F, F, OMe, F, 1-t-butyloxyundecyl), (B654, F, F, OMe, F, 1-t-butyloxydodecyl), (B655, F, F, OMe, F, 1-t-butyloxy-1-cyclohexylmethyl), (B656, F, F, OMe, F, 1-n-pentyloxyethyl), (B657, F, F, OMe, F, 1-n-pentyloxypropyl), (B658, F, F, OMe, F, 3-n-pentyloxypropyl), (B659, F, F, OMe, F, 1-n-pentyloxy-3-methylthiopropyl), (B660, F, F, OMe, F, 1-n-pentyloxybutyl), (B661, F, F, OMe, F, 1-n-pentyloxy-2-methylpropyl), (B662, F, F, OMe, F, 1-n-pentyloxypentyl), (B663, F, F, OMe, F, 1-n-pentyloxy-3-methylbutyl), (B664, F, F, OMe, F, 1-n-pentyloxy-2,2-dimethylpropyl), (B665, F, F, OMe, F, 1-n-pentyloxyhexyl), (B666, F, F, OMe, F, 1-n-pentyloxy-3,3-dimethylbutyl), (B667, F, F, OMe, F, 1-n-pentyloxyheptyl), (B668, F, F, OMe, F, 1-n-pentyloxyoctyl), (B669, F, F, OMe, F, 1-n-pentyloxynonyl), (B670, F, F, OMe, F, 1-n-pentyloxydecyl), (B671, F, F, OMe, F, 1-n-pentyloxyundecyl), (B672, F, F, OMe, F, 1-n-pentyloxydodecyl), (B673, F, F, OMe, F, 1-n-pentyloxy-1-cyclohexylmethyl), (B674, F, F, OMe, F, 1-isopentyloxyproyl), (B675, F, F, OMe, F, 1-neopentyloxyethyl), (B676, F, F, OMe, F, 1-neopentyloxypropyl), (B677, F, F, OMe, F, 1-neopentyloxybutyl), (B678, F, F, OMe, F, 1-neopentyloxy-2-methylpropyl), (B679, F, F, OMe, F, 1-neopentyloxypentyl), (B680, F, F, OMe, F, 1-neopentyloxy-3-methylbutyl), (B681, F, F, OMe, F, 1-neopentyloxy-2,2-dimethylpropyl), (B682, F, F, OMe, F, 1-neopentyloxyhexyl), (B683, F, F, OMe, F, 1-neopentyloxy-3,3-dimethylbutyl), (B684, F, F, OMe, F, 1-neopentyloxyheptyl), (B685, F, F, OMe, F, 1-neopentyloxyoctyl), (B686, F, F, OMe, F, 1-neopentyloxynonyl), (B687, F, F, OMe, F, 1-neopentyloxydecyl), (B688, F, F, OMe, F, 1-neopentyloxyundecyl), (B689, F, F, OMe, F, 1-neopentyloxydodecyl), (B690, F, F, OMe, F, 1-neopentyloxy-1-cyclohexylmethyl), (B691, F, F, OMe, F, 1-n-hexyloxyethyl), (B692, F, F, OMe, F, 1-n-hexyloxypropyl), (B693, F, F, OMe, F, 3-n-hexyloxypropyl), (B694, F, F, OMe, F, 1-n-hexyloxybutyl), (B695, F, F, OMe, F, 1-n-hexyloxy-2-methylpropyl), (B696, F, F, OMe, F, 1-n-hexyloxypentyl), (B697, F, F, OMe, F, 1-n-hexyloxy-3-methylbutyl), (B698, F, F, OMe, F, 1-n-hexyloxy-2,2-dimethylpropyl), (B699, F, F, OMe, F, 1-n-hexyloxyhexyl), (B700, F, F, OMe, F, 1-n-hexyloxy-3,3-dimethylbutyl), (B701, F, F, OMe, F, 1-n-hexyloxyheptyl), (B702, F, F, OMe, F, 1-n-hexyloxyoctyl), (B703, F, F, OMe, F, 1-n-hexyloxynonyl), (B704, F, F, OMe, F, 1-n-hexyloxydecyl), (B705, F, F, OMe, F, 1-n-hexyloxyundecyl), (B706, F, F, OMe, F, 1-n-hexyloxydodecyl), (B707, F, F, OMe, F, 1-n-hexyloxy-1-cyclohexylmethyl), (B708, F, F, OMe, F, 3-isohexyloxyproyl), (B709, F, F, OMe, F, 3-(3,3-dimethylbutyloxy)propyl), (B710, F, F, OMe, F, 3-(2-cyclopentylethyloxy)propyl), (B711, F, F, OMe, F, 1-n-octyloxydodecyl), (B712, F, F, OMe, OMe, 1-methyloxyethyl), (B713, F, F, OMe, OMe, 1-methyloxypropyl), (B714, F, F, OMe, OMe, 1-methyloxy-3-n-hexyloxypropyl), (B715, F, F, OMe, OMe, 1-methyloxybutyl), (B716, F, F, OMe, OMe, 1-methyloxy-4-n-pentyloxybutyl), (B717, F, F, OMe, OMe, 1-methyloxy-2-methylpropyl), (B718, F, F, OMe, OMe, 1-methyloxypentyl), (B719, F, F, OMe, OMe, 1-methyloxy-3-methylbutyl), (B720, F, F, OMe, OMe, 1-methyloxy-2,2-dimethylpropyl), (B721, F, F, OMe,. OMe, 1-methyloxyhexyl), (B722, F, F, OMe, OMe, 4-methyloxyhexyl), (B723, F, F, OMe, OMe, 1-methyloxy-4-methylpentyl), (B724, F, F, OMe, OMe, 1-methyloxy-3,3-dimethylbutyl), (B725, F, F, OMe, OMe, 3-methyloxy-2,4-dimethyl-3-pentyl), (B726, F, F, OMe, OMe, 1-methyloxyheptyl), (B727, F, F, OMe, OMe, 4-methyloxy-4-heptyl), (B728, F, F, OMe, OMe, 1-methyloxyoctyl), (B729, F, F, OMe, OMe, 3-methyloxyoctyl), (B730, F, F, OMe, OMe, 1-methyloxynonyl), (B731, F, F, OMe, OMe, 1-methyloxydecyl), (B732, F, F, OMe, OMe, 1-methyloxyundecyl), (B733, F, F, OMe, OMe, 1-methyloxydodecyl), (B734, F, F, OMe, OMe, 1-methyloxy-1-cyclohexylmethyl), (B735, F, F, OMe, OMe, 1-(4-ethyloxybutyloxy)-1-cyclohexylmethyl), (B736, F, F, OMe, OMe, 1-ethyloxyethyl), (B737, F, F, OMe, OMe, 1-ethyloxypropyl), (B738, F, F, OMe, OMe, 1-(4-ethyloxybutyloxy)propyl), (B739, F, F, OMe, OMe, 1-ethyloxybutyl), (B740, F, F, OMe, OMe, 1-ethyloxy-2-methylpropyl), (B741, F, F, OMe, OMe, 1-ethyloxypentyl), (B742, F, F, OMe, OMe, 1-ethyloxy-3-methylbutyl), (B743, F, F, OMe, OMe, 1-ethyloxy-2,2-dimethylpropyl), (B744, F, F, OMe, OMe, 1-ethyloxyhexyl), (B745, F, F, OMe, OMe, 1-ethyloxy-3,3-dimethylbutyl), (B746, F, F, OMe, OMe, 1-ethyloxyheptyl), (B747, F, F, OMe, OMe, 1-ethyloxyoctyl), (B748, F, F, OMe, OMe, 1-ethyloxynonyl), (B749, F, F, OMe, OMe, 1-ethyloxydecyl), (B750, F, F, OMe, OMe, 1-ethyloxyundecyl), (B751, F, F, OMe, OMe, 1-ethyloxydodecyl), (B752, F, F, OMe, OMe, 1-ethyloxy-1-cyclohexylmethyl), (B753, F, F, OMe, OMe, 1-n-propyloxyethyl), (B754, F, F, OMe, OMe, 1-n-propyloxypropyl), (B755, F, F, OMe, OMe, ³-n-propyloxypropyl), (B756, F, F, OMe, OMe, 1-n-propyloxybutyl), (B757, F, F, OMe, OMe, 1,4-di(n-propyloxy)butyl), (B758, F, F, OMe, OMe, 1-n-propyloxy-2-methylpropyl), (B759, F, F, OMe, OMe, 1-n-propyloxypentyl), (B760, F, F, OMe, OMe, 1-n-propyloxy-3-methylbutyl), (B761, F, F, OMe, OMe, 1-n-propyloxy-2,2-dimethylpropyl), (B762, F, F, OMe, OMe, 1-n-propyloxyhexyl), (B763, F, F, OMe, OMe, 1-n-propyloxy-3,3-dimethylbutyl), (B764, F, F, OMe, OMe, 1-n-propyloxyheptyl), (B765, F, F, OMe, OMe, 1-n-propyloxyoctyl), (B766, F, F, OMe, OMe, 1-n-propyloxynonyl), (B767, F, F, OMe, OMe, 1-n-propyloxydecyl), (B768, F, F, OMe, OMe, 1-n-propyloxyundecyl), (B769, F, F, OMe, OMe, 1-n-propyloxydodecyl), (B770, F, F, OMe, OMe, 1-n-propyloxy-1-cyclohexylmethyl), (B771, F, F, OMe, OMe, 1-isopropyloxyethyl), (B772, F, F, OMe, OMe, 1-isopropyloxypropyl), (B773, F, F, OMe, OMe, 3-isopropyloxypropyl), (B774, F, F, OMe, OMe, 1-isopropyloxybutyl), (B775, F, F, OMe, OMe, 1-isopropyloxy-2-methylpropyl), (B776, F, F, OMe, OMe, 1-isopropyloxypentyl), (B777, F, F, OMe, OMe, 1-isopropyloxy-3-methylbutyl), (B778, F, F, OMe, OMe, 1-isopropyloxy-2,2-dimethylpropyl), (B779, F, F, OMe, OMe, 1-isopropyloxyhexyl), (B780, F, F, OMe, OMe, 1-isopropyloxy-3,3-dimethylbutyl), (B781, F, F, OMe, OMe, 1-isopropyloxyheptyl), (B782, F, F, OMe, OMe, 1-isopropyloxyoctyl), (B783, F, F, OMe, OMe, 1-isopropyloxynonyl), (B784, F, F, OMe, OMe, 1-isopropyloxydecyl), (B785, F, F, OMe, OMe, 1-isopropyloxyundecyl), (B786, F, F, OMe, OMe, 1-isopropyloxydodecyl), (B787, F, F, OMe, OMe, 1-isopropyloxy-1-cyclohexylmethyl), (B788, F, F, OMe, OMe, 1-n-butyloxyethyl), (B789, F, F, OMe, OMe, 1-n-butyloxypropyl), (B791, F, F, OMe, OMe, 1-n-butyloxybutyl), (B792, F, F, OMe, OMe, 1,4-di(n-butyloxy)butyl), (B793, F, F, OMe, OMe, 1-n-butyloxy-2-methylpropyl), (B794, F, F, OMe, OMe, 1-n-butyloxypentyl), (B795, F, F, OMe, OMe, 1-n-butyloxy-3-methylbutyl), (B796, F, F, OMe, OMe, 1-n-butyloxy-2,2-dimethylpropyl), (B797, F, F, OMe, OMe, 1-n-butyloxyhexyl), (B798, F, F, OMe, OMe, 1-n-butyloxy-3,3-dimethylbutyl), (B799, F, F, OMe, OMe, 1-n-butyloxyheptyl), (B800, F, F, OMe, OMe, 1-n-butyloxyoctyl), (B801, F, F, OMe, OMe, 1-n-butyloxynonyl), (B802, F, F, OMe, OMe, 1-n-butyloxydecyl), (B803, F, F, OMe, OMe, 1-n-butyloxyundecyl), (B804, F, F, OMe, OMe, 1-n-butyloxydodecyl), (B805, F, F, OMe, OMe, 1-n-butyloxy-1-cyclohexylmethyl), (B806, F, F, OMe, OMe, 1-isobutyloxyethyl), (B807, F, F, OMe, OMe, 1-isobutyloxypropyl), (B808, F, F, OMe, OMe, 1-isobutyloxybutyl), (B809, F, F, OMe, OMe, 1-isobutyloxy-2-methylpropyl), (B810, F, F, OMe, OMe, 1-isobutyloxypentyl), (B811, F, F, OMe, OMe, 1-isobutyloxy-3-methylbutyl), (B812, F, F, OMe, OMe, 1-isobutyloxy-2,2-dimethylpropyl), (B813, F, F, OMe, OMe, 1-isobutyloxyhexyl), (B814, F, F, OMe, OMe, 1-isobutyloxy-3,3-dimethylbutyl),. (B815, F, F, OMe, OMe, 1-isobutyloxyheptyl), (B816, F, F, OMe, OMe, 1-isobutyloxyoctyl), (B817, F, F, OMe, OMe, 1-isobutyloxyynonyl), (B818, F, F, OMe, OMe, 1-isobutyloxydecyl), (B819, F, F, OMe, OMe, 1-isobutyloxyundecyl), (B820, F, F, OMe, OMe, 1-isobutyloxydodecyl), (B821, F, F, OMe, OMe, 1-isobutyloxy-1-cyclohexylmethyl), (B822, F, F, OMe, OMe, 1-t-butyloxyethyl), (B823, F, F, OMe, OMe, 1-t-butyloxypropyl), (B824, F, F, OMe, OMe, 1-t-butyloxybutyl), (B825, F, F, OMe, OMe, 1-t-butyloxy-2-methylpropyl), (B826, F, F, OMe, OMe, 1-t-butyloxypentyl), (B827, F, F, OMe, OMe, 1-t-butyloxy-3-methylbutyl), (B828, F, F, OMe, OMe, 1-t-butyloxy-2,2-dimethylpropyl), (B829, F, F, OMe, OMe, 1-t-butyloxyhexyl), (B830, F, F, OMe, OMe, 1-t-butyloxy-3,3-dimethylbutyl), (B831, F, F, OMe, OMe, 1-t-butyloxyheptyl), (B832, F, F, OMe, OMe, 1-t-butyloxyoctyl), (B833, F, F, OMe, OMe, 1-t-butyloxynonyl), (B834, F, F, OMe, OMe, 1-t-butyloxydecyl), (B835, F, F, OMe, OMe, 1-t-butyloxyundecyl), (B836, F, F, OMe, OMe, 1-t-butyloxydodecyl), (B837, F, F, OMe, OMe, 1-t-butyloxy-1-cyclohexylmethyl), (B838, F, F, OMe, OMe, 1-n-pentyloxyethyl), (B839, F, F, OMe, OMe, 1-n-pentyloxypropyl), (B840, F, F, OMe, OMe, 3-n-pentyloxypropyl), (B841, F, F, OMe, OMe, 1-n-pentyloxy-3-methylthiopropyl), (B842, F, F, OMe, OMe, 1-n-pentyloxybutyl), (B843, F, F, OMe, OMe, 1-n-pentyloxy-2-methylpropyl), (B844, F, F, OMe, OMe, 1-n-pentyloxypentyl), (B845, F, F, OMe, OMe, 1-n-pentyloxy-3-methylbutyl), (B846, F, F, OMe, OMe, 1-n-pentyloxy-2,2-dimethylpropyl), (B847, F, F, OMe, OMe, 1-n-pentyloxyhexyl), (B848, F, F, OMe, OMe, 1-n-pentyloxy-3,3-dimethylbutyl), (B849, F, F, OMe, OMe, 1-n-pentyloxyheptyl), (B850, F, F, OMe, OMe, 1-n-pentyloxyoctyl), (B851, F, F, OMe, OMe, 1-n-pentyloxynonyl), (B852, F, F, OMe, OMe, 1-n-pentyloxydecyl), (B853, F, F, OMe, OMe, 1-n-pentyloxyundecyl), (B854, F, F, OMe, OMe, 1-n-pentyloxydodecyl), (B855, F, F, OMe, OMe, 1-n-pentyloxy-1-cyclohexylmethyl), (B856, F, F, OMe, OMe, 1-isopentyloxypropyl), (B857, F, F, OMe, OMe, 1-neopentyloxyethyl), (B858, F, F, OMe, OMe, 1-neopentyloxypropyl), (B859, F, F, OMe, OMe, 3-neopentyloxyethyl), (B860, F, F, OMe, OMe, 1-neopentyloxybutyl), (B861, F, F, OMe, OMe, 1-neopentyloxy-2-methylpropyl), (B862, F, F, OMe, OMe, 1-neopentyloxypentyl), (B863, F, F, OMe, OMe, 1-neopentyloxy-3-methylbutyl), (B864, F, F, OMe, OMe, 1-neopentyloxy-2,2-dimethylpropyl), (B865, F, F, OMe, OMe, 1-neopentyloxyhexyl), (B866, F, F, OMe, OMe, 1-neopentyloxy-3,3-dimethylbutyl), (B867, F, F, OMe, OMe, 1-neopentyloxyheptyl), (B868, F, F, OMe, OMe, 1-neopentyloxyoctyl), (B869, F, F, OMe, OMe, 1-neopentyloxynonyl), (B870, F, F, OMe, OMe, 1-neopentyloxydecyl), (B871, F, F, OMe, OMe, 1-neopentyloxyundecyl), (B872, F, F, OMe, OMe, 1-neopentyloxydodecyl), (B873, F, F, OMe, OMe, 1-neopentyloxy-1-cyclohexylmethyl), (B874, F, F, OMe, OMe, 1-n-hexyloxyethyl), (B875, F, F, OMe, OMe, 1-n-hexyloxypropyl), (B876, F, F, OMe, OMe, 3-n-hexyloxypropyl), (B877, F, F, OMe, OMe, 1-n-hexyloxybutyl), (B878, F, F, OMe, OMe, 1-n-hexyloxy-2-methylpropyl), (B879, F, F, OMe, OMe, 1-n-hexyloxypentyl), (B880, F, F, OMe, OMe, 1-n-hexyloxy-3-methylbutyl), (B881, F, F, OMe, OMe, 1-n-hexyloxy-2,2-dimethylpropyl), (B882, F, F, OMe, OMe, 1-n-hexyloxyhexyl), (B883, F, F, OMe, OMe, 1-n-hexyloxy-3,3-dimethylbutyl), (B884, F, F, OMe, OMe, 1-n-hexyloxyheptyl), (B885, F, F, OMe, OMe, 1-n-hexyloxyoctyl), (B886, F, F, OMe, OMe, 1-n-hexyloxynonyl), (B887, F, F, OMe, OMe, 1-n-hexyloxydecyl), (B888, F, F, OMe, OMe, 1-n-hexyloxyundecyl), (B889, F, F, OMe, OMe, 1-n-hexyloxydodecyl), (B890, F, F, OMe, OMe, 1-n-hexyloxy-1-cyclohexylmethyl), (B891, F, F, OMe, OMe, 3-isohexyloxypropyl), (B892, F, F, OMe, OMe, 3-(3,3-dimethylbutyloxy)propyl), (B893, F, F, OMe, OMe, 3-(2-cyclopentylethyloxy)propyl), (B894, F, F, OMe, OMe, 1-n-octyloxyethyl), (B895, Cl, Cl, Me, F, 1-methyloxyethyl), (B898, Cl, Cl, Me, F, 1-methyloxybutyl), (B900, Cl, Cl, Me, F, 1-methyloxy-2-methylpropyl), (B901, Cl, Cl, Me, F, 1-methyloxypentyl), (B902, Cl, Cl, Me, F, 1-methyloxy-3-methylbutyl), (B903, Cl, Cl, Me, F, 3-methyloxy-3-methylbutyl), (B904, Cl, Cl, Me, F, 4-methyloxyhexyl), (B906, Cl, Cl, Me, F, 1-methyloxy-1-cyclohexylmethyl), (B907, Cl, Cl, Me, F, 1-(4-ethyloxybutyloxy)-1-cyclohexylmethyl), (B908, Cl, Cl, Me, F, 1-ethyloxyethyl), (B909, Cl, Cl, Me, F, 1-ethyloxypropyl), (B910, Cl, Cl, Me, F, 1-ethyloxy-3-n-hexyloxypropyl), (B911, Cl, Cl, Me, F, 1-ethyloxybutyl), (B912, Cl, Cl, Me, F, 1-ethyloxy-4-n-pentyloxybutyl), (B913, Cl, Cl, Me, F, 1-ethyloxy-2-methylpropyl), (B914, Cl, Cl, Me, F, 1-ethyloxy-3-methylbutyl), (B915, Cl, Cl, Me, F, 1-ethyloxyhexyl), (B916, Cl, Cl, Me, F, 1-ethyloxyheptyl), (B917, Cl, Cl, Me, F, 1-ethyloxyoctyl), (B918, Cl, Cl, Me, F, 1-ethyloxynonyl), (B919, Cl, Cl, Me, F, 1-ethyloxydecyl), (B920, Cl, Cl, Me, F, 1-ethyloxyundecyl), (B921, Cl, Cl, Me, F, 1-ethyloxydodecyl), (B922, Cl, Cl, Me, F, 1-ethyloxy-1-cyclohexylmethyl), (B923, Cl, Cl, Me, F, 1-n-propyloxy-3-n-hexyloxypropyl), (B924, Cl, Cl, Me, F, 1-n-propyloxy-4-n-pentyloxybutyl), (B925, Cl, Cl, Me, F, 1-n-propyloxy-2-methylpropyl), (B926, Cl, Cl, Me, F, 1-n-propyloxy-3-methylbutyl), (B928, Cl, Cl, Me, F, 1-n-propyloxyhexyl), (B929, Cl, Cl, Me, F, 1-n-propyloxy-3,3-dimethylbutyl), (B930, Cl, Cl, Me, F, 1-n-propyloxyheptyl), (B931, Cl, Cl, Me, F, 1-n-propyloxyoctyl), (B932, Cl, Cl, Me, F, 1-n-propyloxynonyl), (B933, Cl, Cl, Me, F, 1-n-propyloxydecyl), (B934, Cl, Cl, Me, F, 1-n-propyloxyundecyl), (B935, Cl, Cl, Me, F, 1-n-propyloxydodecyl), (B937, Cl, Cl, Me, F, 1-isopropyloxyethyl), (B938, Cl, Cl, Me, F, 1-isopropyloxypropyl), (B939, Cl, Cl, Me, F, 1-isopropyloxy-3-n-hexyloxypropyl), (B940, Cl, Cl, Me, F, 1-isopropyloxybutyl), (B941, Cl, Cl, Me, F, 1-isopropyloxy-4-n-pentyloxybutyl), (B942, Cl, Cl, Me, F, 1-isopropyloxy-2-methylpropyl), (B943, Cl, Cl, Me, F, 1-isopropyloxypentyl), (B944, Cl, Cl, Me, F, 1-isopropyloxy-3-methylbutyl), (B945, Cl, Cl, Me, F, 1-isopropyloxy-2,2-dimethylpropyl), (B946, Cl, Cl, Me, F, 1-isopropyloxyhexyl), (B947, Cl, Cl, Me, F, 1-isopropyloxy-3,3-dimethylbutyl), (B948, Cl, Cl, Me, F, 1-isopropyloxyheptyl), (B949, Cl, Cl, Me, F, 1-isopropyloxyoctyl), (B950, Cl, Cl, Me, F, 1-isopropyloxynonyl), (B951, Cl, Cl, Me, F, 1-isopropyloxydecyl), (B952, Cl, Cl, Me, F, 1-isopropyloxyundecyl), (B953, Cl, Cl, Me, F, 1-isopropyloxydodecyl), (B954, Cl, Cl, Me, F, 1-isopropyloxy-1-cyclohexylmethyl), (B955, Cl, Cl, Me, F, 1,4-di(n-butyloxy)butyl), (B956, Cl, Cl, . Me, F, 1-n-butyloxy-2-methylpropyl), (B957, Cl, Cl, Me, F, 1-n-butyloxy-3-methylbutyl), (B959, Cl, Cl, Me, F, 1-n-butyloxyhexyl), (B960, Cl, Cl, Me, F, 1-n-butyloxy-3,3-dimethylbutyl), (B961, Cl, Cl, Me, F, 1-n-butyloxyheptyl), (B962, Cl, Cl, Me, F, 1-n-butyloxyoctyl), (B963, Cl, Cl, Me, F, 1-n-butyloxynonyl), (B964, Cl, Cl, Me, F, 1-n-butyloxydecyl), (B965, Cl, Cl, Me, F, 1-n-butyloxyundecyl), (B966, Cl, Cl, Me, F, 1-n-butyloxydodecyl), (B968, Cl, Cl, Me, F, 1-isobutyloxyethyl), (B969, Cl, Cl, Me, F, 1-isobutyloxypropyl), (B970, Cl, Cl, Me, F, 1-isobutyloxybutyl), (B971, Cl, Cl, Me, F, 1-isobutyloxy-2-methylpropyl), (B972, Cl, Cl, Me, F, 1-isobutyloxypentyl), (B973, Cl, Cl, Me, F, 1-isobutyloxy-3-methylbutyl), (B974, Cl, Cl, Me, F, 1-isobutyloxy-2,2-dimethylpropyl), (B975, Cl, Cl, Me, F, 1-isobutyloxyhexyl), (B976, Cl, Cl, Me, F, 1-isobutyloxy-3,3-dimethylbutyl), (B977, Cl, Cl, Me, F, 1-isobutyloxyheptyl), (B978, Cl, Cl, Me, F, 1-isobutyloxyoctyl), (B979, Cl, Cl, Me, F, 1-isobutyloxyynonyl), (B980, Cl, Cl, Me, F, 1-isobutyloxydecyl), (B981, Cl, Cl, Me, F, 1-isobutyloxyundecyl), (B982, Cl, Cl, Me, F, 1-isobutyloxydodecyl), (B983, Cl, Cl, Me, F, 1-isobutox-1-cyclohexylymethyl), (B984, Cl, Cl, Me, F, 1-t-butyloxyethyl), (B985, Cl, Cl, Me, F, 1-t-butyloxypropyl), (B986, Cl, Cl, Me, F, 1-t-butyloxybutyl), (B987, Cl, Cl, Me, F, 1-t-butyloxy-2-methylpropyl), (B988, Cl, Cl, Me, F, 1-t-butyloxypentyl), (B989, Cl, Cl, Me, F, 1-t-butyloxy-3-methylbutyl), (B990, Cl, Cl, Me, F, 1-t-butyloxy-2,2-dimethylpropyl), (B991, Cl, Cl, Me, F, 1-t-butyloxyhexyl), (B992, Cl, Cl, Me, F, 1-t-butyloxy-3,3-dimethylbutyl), (B993, Cl, Cl, Me, F, 1-t-butyloxyheptyl), (B994, Cl, Cl, Me, F, 1-t-butyloxyoctyl), (B995, Cl, Cl, Me, F, 1-t-butyloxynonyl), (B996, Cl, Cl, Me, F, 1-t-butyloxydecyl), (B997, Cl, Cl, Me, F, 1-t-butyloxyundecyl), (B998, Cl, Cl, Me, F, 1-t-butyloxydodecyl), (B999, Cl, Cl, Me, F, 1-t-butyloxy-1-cyclohexylmethyl), (B1000, Cl, Cl, Me, F, 1-n-pentyloxyethyl), (B1001, Cl, Cl, Me, F, 1-n-pentyloxy-2-methylpropyl), (B1002, Cl, Cl, Me, F, 1-n-pentyloxy-3-methylbutyl), (B1003, Cl, Cl, Me, F, 1-n-pentyloxy-2,2-dimethylpropyl), (B1004, Cl, Cl, Me, F, 1-n-pentyloxyhexyl), (B1005, Cl, Cl, Me, F, 1-n-pentyloxy-3,3-dimethylbutyl), (B1006, Cl, Cl, Me, F, 1-n-pentyloxyheptyl), (B1007, Cl, Cl, Me, F, 1-n-pentyloxyoctyl), (B1008, Cl, Cl, Me, F, 1-n-pentyloxynonyl), (B 1009, Cl, Cl, Me, F, 1-n-pentyloxydecyl), (B1010, Cl, Cl, Me, F, 1-n-pentyloxyundecyl), (B1011, Cl, Cl, Me, F, 1-n-pentyloxydodecyl), (B1012, Cl, Cl, Me, F, 1-n-pentyloxy-1-cyclohexylmethyl), (B1013, Cl, Cl, Me, F, 1-neopentyloxyethyl), (B1014, Cl, Cl, Me, F, 1-neopentyloxypropyl), (B1015, Cl, Cl, Me, F, 1-neopentyloxybutyl), (B1016, Cl, Cl, Me, F, 1-neopentyloxy-2-methylpropyl), (B1017, Cl, Cl, Me, F, 1-neopentyloxypentyl), (B1018, Cl, Cl, Me, F, 1-neopentyloxy-3-methylbutyl), (B1019, Cl, Cl, Me, F, 1-neopentyloxy-2,2-dimethylpropyl), (B1020, Cl, Cl, Me, F, 1-neopentyloxyhexyl), (B1021, Cl, Cl, Me, F, 1-neopentyloxy-3,3-dimethylbutyl), (B1022, Cl, Cl, Me, F, 1-neopentyloxyheptyl), (B 1023, Cl, Cl, Me, F, 1-neopentyloxyoctyl), (B1024, Cl, Cl, Me, F, 1-neopentyloxynonyl), (B1025, Cl, Cl, Me, F, 1-neopentyloxydecyl), (B 1026, Cl, Cl, Me, F, 1-neopentyloxyundecyl), (B1027, Cl, Cl, Me, F, 1-neopentyloxydodecyl), (B1028, Cl, Cl, Me, F, 1-neopentyloxy-1-cyclohexylmethyl), (B1029, Cl, Cl, Me, F, 1-n-hexyloxybutyl), (B1030, Cl, Cl, Me, F, 1-n-hexyloxy-2-methylpropyl), (B1031, Cl, Cl, Me, F, 1-n-hexyloxypentyl), (B1032, Cl, Cl, Me, F, 1-n-hexyloxy-3-methylbutyl), (B1033, Cl, Cl, Me, F, 1-n-hexyloxy-2,2-dimethylpropyl), (B 1034, Cl, Cl, Me, F, 1-n-hexyloxyhexyl), (B1035, Cl, Cl, Me, F, 1-n-hexyloxy-3,3-dimethylbutyl), (B1036, Cl, Cl, Me, F, 1-n-hexyloxyheptyl), (B1037, Cl, Cl, Me, F, 1-n-hexyloxyoctyl), (B1038, Cl, Cl, Me, F, 1-n-hexyloxynonyl), (B1039, Cl, Cl, Me, F, 1-n-hexyloxydecyl), (B1040, Cl, Cl, Me, F, 1-n-hexyloxyundecyl), (B1041, Cl, Cl, Me, F, 1-n-hexyloxydodecyl), (B1042, Cl, Cl, Me, F, 1-n-hexyloxy-1-cyclohexylmethyl), (B1043, Cl, Cl, Me, OMe, 1-methyloxyethyl), (B1044, Cl, Cl, Me, OMe, 1-methyloxypropyl), (B1045, Cl, Cl, Me, OMe, 1-methyloxy-3-n-hexyloxypropyl), (B1046, Cl, Cl, Me, OMe, 1-methyloxybutyl), (B1047, Cl, Cl, Me, OMe, 1-methyloxy-4-n-pentyloxybutyl), (B1048, Cl, Cl, Me, OMe, 1-methyloxy-2-methylpropyl), (B1049, Cl, Cl, Me, OMe, 1-methyloxypentyl), (B1050, Cl, Cl, Me, OMe, 1-methyloxy-3-methylbutyl), (B1051, Cl, Cl, Me, OMe, 1-methyloxy-2,2-dimethylpropyl), (B1052, Cl, Cl, Me, OMe, 1-methyloxyhexyl), (B1055, Cl, Cl, Me, OMe, 1-methyloxyheptyl), (B1056, Cl, Cl, Me, OMe, 1-methyloxyoctyl), (B1057, Cl, Cl, Me, OMe, 3-methyloxyoctyl), (B1058, Cl, Cl, Me, OMe, 1-methyloxynonyl), (B1061, Cl, Cl, Me, OMe, 1-methyloxydodecyl), (B1062, Cl, Cl, Me, OMe, 1-methyloxy-1-cyclohexylmethyl), (B1063, Cl, Cl, Me, OMe, 1-(4-ethyloxybutyloxy)-1-cyclohexylmethyl), (B1064, Cl, Cl, Me, OMe, 1-ethyloxyethyl), (B1065, Cl, Cl, Me, OMe, 1-ethyloxypropyl), (B1066, Cl, Cl, Me, OMe, 1-ethyloxy-3-n-hexyloxypropyl), (B1067, Cl, Cl, Me, OMe, 1-(4-ethyloxybutyloxy)propyl), (B1068, Cl, Cl, Me, OMe, 1-ethyloxybutyl), (B1069, Cl, Cl, Me, OMe, 1-ethyloxy-4-n-pentyloxybutyl), (B1070, Cl, Cl, Me, OMe, 1-ethyloxy-2-methylpropyl), (B1071, Cl, Cl, Me, OMe, 1-ethyloxypentyl), (B1072, Cl, Cl, Me, OMe, 1-ethyloxy-3-methylbutyl), (B 1073, Cl, Cl, Me, OMe, 1-ethyloxy-2,2-dimethylpropyl), (B1074, Cl, Cl, Me, OMe, 1-ethyloxyhexyl), (B1075, Cl, Cl, Me, OMe, 1-ethyloxy-3,3-dimethylbutyl), (B1076, Cl, Cl, Me, OMe, 1-ethyloxyheptyl), (B1077, Cl, Cl, Me, OMe, 1-ethyloxyoctyl), (B1078, Cl, Cl, Me, OMe, 1-ethyloxynonyl), (B1079, Cl, Cl, Me, OMe, 1-ethyloxydecyl), (B1080, Cl, Cl, Me, OMe, 1-ethyloxyundecyl), (B1081, Cl, Cl, Me, OMe, 1-ethyloxydodecyl), (B1082, Cl, Cl, Me, OMe, 1-ethyloxy-1-cyclohexylmethyl), (B1083, Cl, Cl, Me, OMe, 1-n-propyloxyethyl), (B1084, Cl, Cl, Me, OMe, 1-n-propyloxypropyl), (B1085, Cl, Cl, Me, OMe, 3-n-propyloxypropyl), (B1086, Cl, Cl, Me, OMe, 1-n-propyloxy-3-n-hexyloxypropyl), (B1087, Cl, Cl, Me, OMe, 1-n-propyloxybutyl), (B1088, Cl, Cl, Me, OMe, 1-n-propyloxy-4-n-pentyloxybutyl), (B1089, Cl, Cl, Me, OMe, 1,4-di(n-propyloxy)butyl), (B1090, Cl, Cl, Me, OMe, 1-n-propyloxy-2-methylpropyl), (B1091, Cl, Cl, Me, OMe, 1-n-propyloxypentyl), (B1092, Cl, Cl, Me, OMe, 1-n-propyloxy-3-methylbutyl), (B1093, Cl, Cl, Me, OMe, 1-n-propyloxy-2,2-dimethylpropyl), (B1094, Cl, Cl, Me, OMe, 1-n-propyloxyhexyl), (B1095, Cl, Cl, Me, OMe, 1-n-propyloxy-3,3-dimethylbutyl), (B1096, Cl, Cl, Me, OMe, 1-n-propyloxyheptyl), (B1097, Cl, Cl, Me, OMe, 1-n-propyloxyoctyl), (B1098, Cl, Cl, Me, OMe, 1-n-propyloxynonyl), (B1099, Cl, Cl, Me, OMe, 1-n-propyloxydecyl), (B1100, Cl, Cl, Me, OMe, 1-n-propyloxyundecyl), (B1101, Cl, Cl, Me, OMe, 1-n-propyloxydodecyl), (B1103, Cl, Cl, Me, OMe, 1-isopropyloxyethyl), (B1104, Cl, Cl, Me, OMe, 1-isopropyloxypropyl), (B1105, Cl, Cl, Me, OMe, 3-isopropyloxypropyl), (B 1106, Cl, Cl, Me, OMe, 1-isopropyloxy-3-n-hexyloxypropyl), (B1107, Cl, Cl, Me, OMe, 1-isopropyloxybutyl), (B1108, Cl, Cl, Me, OMe, 1-isopropyloxy-4-n-pentyloxybutyl), (B 1109, Cl, Cl, Me, OMe, 1-isopropyloxy-2-methylpropyl), (B1110, Cl, Cl, Me, OMe, 1-isopropyloxypentyl), (B111, Cl, Cl, Me, OMe, 1-isopropyloxy-3-methylbutyl), (B 1112, Cl, Cl, Me, OMe, 1-isopropyloxy-2,2-dimethylpropyl), (B1113, Cl, Cl, Me, OMe, 1-isopropyloxyhexyl), (B1114, Cl, Cl, Me, OMe, 1-isopropyloxy-3,3-dimethylbutyl), (B1115, Cl, Cl, Me, OMe, 1-isopropyloxyheptyl), (B1116, Cl, Cl, Me, OMe, 1-isopropyloxyoctyl), (B1117, Cl, Cl, Me, OMe, 1-isopropyloxynonyl), (B1118, Cl, Cl, Me, OMe, 1-isopropyloxydecyl), (B1119, Cl, Cl, Me, OMe, 1-isopropyloxyundecyl), (B1120, Cl, Cl, Me, OMe, 1-isopropyloxydodecyl), (B1121, Cl, Cl, Me, OMe, 1-isopropyloxy-1-cyclohexylmethyl), (B1123, Cl, Cl, Me, OMe, 1-n-butyloxypropyl), (B1125, Cl, Cl, Me, OMe, 1,4-di(n-butyloxy)butyl), (B1126, Cl, Cl, Me, OMe, 1-n-butyloxybutyl), (B1127, Cl, Cl, Me, OMe, 1-n-butyloxy-2-methylpropyl), (B1128, Cl, Cl, Me, OMe, 1-n-butyloxypentyl), (B1129, Cl, Cl, Me, OMe, 1-n-butyloxy-3-methylbutyl), (B1130, Cl, Cl, Me, OMe, 1-n-butyloxy-2,2-dimethylpropyl), (B1131, Cl, Cl, Me, OMe, 1-n-butyloxyhexyl), (B1132, Cl, Cl, Me, OMe, 1-n-butyloxy-3,3-dimethylbutyl), (B1133, Cl, Cl, Me, OMe, 1-n-butyloxyheptyl), (B1134, Cl, Cl, Me, OMe, 1-n-butyloxyoctyl), (B1135, Cl, Cl, Me, OMe, 1-n-butyloxynonyl), (B1136, Cl, Cl, Me, OMe, 1-n-butyloxydecyl), (B1137, Cl, Cl, Me, OMe, 1-n-butyloxyundecyl), (B1138, Cl, Cl, Me, OMe, 1-n-butyloxydodecyl), (B1139, Cl, Cl, Me, OMe, 1-n-butyloxy-1-cyclohexylmethyl), (B1140, Cl, Cl, Me, OMe, 1-isobutyloxyethyl), (B1141, Cl, Cl, Me, OMe, 1-isobutyloxypropyl), (B1142, Cl, Cl, Me, OMe, 1-isobutyloxybutyl), (B1143, Cl, Cl, Me, OMe, 1-isobutyloxy-2-methylpropyl), (B1144, Cl, Cl, Me, OMe, 1-isobutyloxypentyl), (B1145, Cl, Cl, Me, OMe, 1-isobutyloxy-3-methylbutyl), (B1146, Cl, Cl, Me, OMe, 1-isobutyloxy-2,2-dimethylpropyl), (B1147, Cl, Cl, Me, OMe, 1-isobutyloxyhexyl), (B1148, Cl, Cl, Me, OMe, 1-isobutyloxy-3,3-dimethylbutyl), (B1149, Cl, Cl, Me, OMe, 1-isobutyloxyheptyl), (B1150, Cl, Cl, Me, OMe, 1-isobutyloxyoctyl), (B1151, Cl, Cl, Me, OMe, 1-isobutyloxyynonyl), (B1152, Cl, Cl, Me, OMe, 1-isobutyloxydecyl), (B1153, Cl, Cl, Me, OMe, 1-isobutyloxyundecyl), (B1154, Cl, Cl, Me, OMe, 1-isobutyloxydodecyl), (B1155, Cl, Cl, Me, OMe, 1-isobutyloxy-1-cyclohexylmethyl), (B1156, Cl, Cl, Me, OMe, 1-t-butyloxyethyl), (B1157, Cl, Cl, Me, OMe, 1-t-butyloxypropyl), (B1158, Cl, Cl, Me, OMe, 1-t-butyloxybutyl), (B1159, Cl, Cl, Me, OMe, 1-t-butyloxy-2-methylpropyl), (B1160, Cl, Cl, Me, OMe, 1-t-butyloxypentyl), (B1161, Cl, Cl, Me, OMe, 1-t-butyloxy-3-methylbutyl), (B1162, Cl, Cl, Me, OMe, 1-t-butyloxy-2,2-dimethylpropyl), (B1163, Cl, Cl, Me, OMe, 1-t-butyloxyhexyl), (B1164, Cl, Cl, Me, OMe, 1-t-butyloxy-3,3-dimethylbutyl), (B1165, Cl, Cl, Me, OMe, 1-t-butyloxyheptyl), (B1166, Cl, Cl, Me, OMe, 1-t-butyloxyoctyl), (B1167, Cl, Cl, Me, OMe, 1-t-butyloxynonyl), (B1168, Cl, Cl, Me, OMe, 1-t-butyloxydecyl), (B1169, Cl, Cl, Me, OMe, 1-t-butyloxyundecyl), (B1170, Cl, Cl, Me, OMe, 1-t-butyloxydodecyl), (B1171, Cl, Cl, Me, OMe, 1-t-butyloxy-1-cyclohexylmethyl), (B1172, Cl, Cl, Me, OMe, 1-n-pentyloxyethyl), (B1173, Cl, Cl, Me, OMe, 1-n-pentyloxypropyl), (B1174, Cl, Cl, Me, OMe, 3-n-pentyloxypropyl), (B1175, Cl, Cl, Me, OMe, 1-n-pentyloxy-3-methylthiopropyl), (B1176, Cl, Cl, Me, OMe, 1-n-pentyloxybutyl), (B1177, Cl, Cl, Me, OMe, 1-n-pentyloxy-2-methylpropyl), (B1178, Cl, Cl, Me, OMe, 1-n-pentyloxypentyl), (B1179, Cl, Cl, Me, OMe, 1-n-pentyloxy-3-methylbutyl), (B1180, Cl, Cl, Me, OMe, 1-n-pentyloxy-2,2-dimethylpropyl), (B1181, Cl, Cl, Me, OMe, 1-n-pentyloxyhexyl), (B1182, Cl, Cl, Me, OMe, 1-n-pentyloxy-3,3-dimethylbutyl), (B1183, Cl, Cl, Me, OMe, 1-n-pentyloxyheptyl), (B1184, Cl, Cl, Me, OMe, 1-n-pentyloxyoctyl), (B1185, Cl, Cl, Me, OMe, 1-n-pentyloxynonyl), (B1186, Cl, Cl, Me, OMe, 1-n-pentyloxydecyl), (B1187, Cl, Cl, Me, OMe, 1-n-pentyloxyundecyl), (B1188, Cl, Cl, Me, OMe, 1-n-pentyloxydodecyl), (B1189, Cl, Cl, Me, OMe, 1-n-pentyloxy-1-cyclohexylmethyl), (B1190, Cl, Cl, Me, OMe, 1-isopentyloxypropyl), (B1191, Cl, Cl, Me, OMe, 1-neopentyloxyethyl), (B1192, Cl, Cl, Me, OMe, 1-neopentyloxypropyl), (B1193, Cl, Cl, Me, OMe, 3-neopentyloxypropyl), (B1194, Cl, Cl, Me, OMe, 1-neopentyloxybutyl), (B1195, Cl, Cl, Me, OMe, 1-neopentyloxy-2-methylpropyl), (B1196, Cl, Cl, Me, OMe, 1-neopentyloxypentyl), (B1197, Cl, Cl, Me, OMe, 1-neopentyloxy-3-methylbutyl), (B1198, Cl, Cl, Me, OMe, 1-neopentyloxy-2,2-dimethylpropyl), (B1199, Cl, Cl, Me, OMe, 1-neopentyloxyhexyl), (B1200, Cl, Cl, Me, OMe, 1-neopentyloxy-3,3-dimethylbutyl), (B1201, Cl, Cl, Me, OMe, 1-neopentyloxyheptyl), (B1202, Cl, Cl, Me, OMe, 1-neopentyloxyoctyl), (B1203, Cl, Cl, Me, OMe, 1-neopentyloxynonyl), (B1204, Cl, Cl, Me, OMe, 1-neopentyloxydecyl), (B1205, Cl, Cl, Me, OMe, 1-neopentyloxyundecyl), (B1206, Cl, Cl, Me, OMe, 1-neopentyloxydodecyl), (B1207, Cl, Cl, Me, OMe, 1-neopentyloxy-1-cyclohexylmethyl), (B1208, Cl, Cl, Me, OMe, 1-n-hexyloxyethyl), (B1209, Cl, Cl, Me, OMe, 1-n-hexyloxypropyl), (B1210, Cl, Cl, Me, OMe, 3-n-hexyloxypropyl), (B1211, Cl, Cl, Me, OMe, 1-n-hexyloxybutyl), (B1212, Cl, Cl, Me, OMe, 1-n-hexyloxy-2-methylpropyl), (B1213, Cl, Cl, Me, OMe, 1-n-hexyloxypentyl), (B1214, Cl, Cl, Me, OMe, 1-n-hexyloxy-3-methylbutyl), (B1215, Cl, Cl, Me, OMe, 1-n-hexyloxy-2,2-dimethylpropyl), (B1216, Cl, Cl, Me, OMe, 1-n-hexyloxyhexyl), (B1217, Cl, Cl, Me, OMe, 1-n-hexyloxy-3,3-dimethylbutyl), (B 1218, Cl, Cl, Me, OMe, 1-n-hexyloxyheptyl), (B 1219, Cl, Cl, Me, OMe, 1-n-hexyloxyoctyl), (B1220, Cl, Cl, Me, OMe, 1-n-hexyloxynonyl), (B1221, Cl, Cl, Me, OMe, 1-n-hexyloxydecyl), (B1222, Cl, Cl, Me, OMe, 1-n-hexyloxyundecyl), (B1223, Cl, Cl, Me, OMe, 1-n-hexyloxydodecyl), (B1224, Cl, Cl, Me, OMe, 1-n-hexyloxy-1-cyclohexylmethyl), (B1225, Cl, Cl, Me, OMe, 3-isohexyloxydodecyl), (B1226, Cl, Cl, Me, OMe, 3-(3,3-dimethylbutyloxy)propyl), (B1227, Cl, Cl, Me, OMe, 3-(2-cyclopentylethyloxy)propyl), (B1228, Cl, Cl, Me, OMe, 1-n-octyloxydodecyl), (B1229, Cl, Cl, OMe, F, 1-methyloxyethyl), (B1230, Cl, Cl, OMe, F, 1-methyloxypropyl), (B1231, Cl, Cl, OMe, F, 1-methyloxy-3-n-hexyloxypropyl), (B1232, Cl, Cl, OMe, F, 1-methyloxybutyl), (B1233, Cl, Cl, OMe, F, 1-methyloxy-4-n-pentyloxybutyl), (B1234, Cl, Cl, OMe, F, 1-methyloxy-2-methylpropyl), (B1235, Cl, Cl, OMe, F, 1-methyloxypentyl), (B1236, Cl, Cl, OMe, F, 1-methyloxy-3-methylbutyl), (B1237, Cl, Cl, OMe, F, 1-methyloxy-2,2-dimethylpropyl), (B1239, Cl, Cl, OMe, F, 4-methyloxyhexyl), (B1240, Cl, Cl, OMe, F, 1-methyloxy-4-methylpentyl), (B1241, Cl, Cl, OMe, F, 1-methyloxy-3,3-dimethylbutyl), (B1242, Cl, Cl, OMe, F, 3-methyloxy-2,4-dimethyl-3-pentyl), (B1243, Cl, Cl, OMe, F, 1-methyloxyheptyl), (B1244, Cl, Cl, OMe, F, 4-methyloxy-4-heptyl), (B1245, Cl, Cl, OMe, F, 1-methyloxyoctyl), (B1246, Cl, Cl, OMe, F, 3-methyloxyoctyl), (B1247, Cl, Cl, OMe, F, 1-methyloxynonyl), (B1248, Cl, Cl, OMe, F, 1-methyloxydecyl), (B1249, Cl, Cl, OMe, F, 1-methyloxyundecyl), (B1251, Cl, Cl, OMe, F, 1-methyloxy-1-cyclohexylmethyl), (B1252, Cl, Cl, OMe, F, 1-(4-ethyloxybutyloxy)-1-cyclohexylmethyl), (B1253, Cl, Cl, OMe, F, 1-ethyloxyethyl), (B1254, Cl, Cl, OMe, F, 1-ethyloxypropyl), (B1255, Cl, Cl, OMe, F, 1-ethyloxy-3-n-hexyloxypropyl), (B1256, Cl, Cl, OMe, F, 1-(4-ethyloxybutyloxy)propyl), (B1257, Cl, Cl, OMe, F, 1-ethyloxybutyl), (B1258, Cl, Cl, OMe, F, 1-ethyloxy-4-n-pentyloxybutyl), (B1259, Cl, Cl, OMe, F, 1-ethyloxy-2-methylpropyl), (B1260, Cl, Cl, OMe, F, 1-ethyloxypentyl), (B1261, Cl, Cl, OMe, F, 1-ethyloxy-3-methylbutyl), (B1262, Cl, Cl, OMe, F, 1-ethyloxy-2,2-dimethylpropyl), (B1263, Cl, Cl, OMe, F, 1-ethyloxyhexyl), (B1264, Cl, Cl, OMe, F, 1-ethyloxy-3,3-dimethylbutyl), (B1265, Cl, Cl, OMe, F, 1-ethyloxyheptyl), (B1266, Cl, Cl, OMe, F, 1-ethyloxyoctyl), (B1267, Cl, Cl, OMe, F, 1-ethyloxynonyl), (B1268, Cl, Cl, OMe, F, 1-ethyloxydecyl), (B1269, Cl, Cl, OMe, F, 1-ethyloxyundecyl), (B1270, Cl, Cl, OMe, F, 1-ethyloxydodecyl), (B1271, Cl, Cl, OMe, F, 1-ethyloxy-1-cyclohexylmethyl), (B1272, Cl, Cl, OMe, F, 1-n-propyloxyethyl), (B1273, Cl, Cl, OMe, F, 1-n-propyloxypropyl), (B1274, Cl, Cl, OMe, F, 3-n-propyloxypropyl), (B1275, Cl, Cl, OMe, F, 1-n-propyloxy-3-n-hexyloxypropyl), (B1276, Cl, Cl, OMe, F, 1-n-propyloxybutyl), (B1277, Cl, Cl, OMe, F, 1-n-propyloxy-4-n-pentyloxybutyl), (B 1278, Cl, Cl, OMe, F, 1,4-di(n-propyloxy)butyl), (B1279, Cl, Cl, OMe, F, 1-n-propyloxy-2-methylpropyl), (B 1280, Cl, Cl, OMe, F, 1-n-propyloxypentyl), (B1281, Cl, Cl, OMe, F, 1-n-propyloxy-3-methylbutyl), (B1282, Cl, Cl, OMe, F, 1-n-propyloxy-2,2-dimethylpropyl), (B1283, Cl, Cl, OMe, F, 1-n-propyloxyhexyl), (B1284, Cl, Cl, OMe, F, 1-n-propyloxy-3,3-dimethylbutyl), (B1285, Cl, Cl, OMe, F, 1-n-propyloxyheptyl), (B1286, Cl, Cl, OMe, F, 1-n-propyloxyoctyl), (B1287, Cl, Cl, OMe, F, 1-n-propyloxynonyl), (B1288, Cl, Cl, OMe, F, 1-n-propyloxydecyl), (B1289, Cl, Cl, OMe, F, 1-n-propyloxyundecyl), (B1290, Cl, Cl, OMe, F, 1-n-propyloxydodecyl), (B1291, Cl, Cl, OMe, F, 1-n-propyloxy-1-cyclohexylmethyl), (B1292, Cl, Cl, OMe, F, 1-isopropyloxyethyl), (B1293, Cl, Cl, OMe, F, 1-isopropyloxypropyl), (B1294, Cl, Cl, OMe, F, 3-isopropyloxypropyl), (B1295, Cl, Cl, OMe, F, 1-isopropyloxy-3-n-hexyloxypropyl), (B1296, Cl, Cl, OMe, F, 1-isopropyloxybutyl), (B1297, Cl, Cl, OMe, F, 1-isopropyloxy-4-n-pentyloxybutyl), (B1298, Cl, Cl, OMe, F, 1-isopropyloxy-2-methylpropyl), (B1299, Cl, Cl, OMe, F, 1-isopropyloxypentyl), (B1300, Cl, Cl, OMe, F, 1-isopropyloxy-3-methylbutyl), (B1301, Cl, Cl, OMe, F, 1-isopropyloxy-2,2-dimethylpropyl), (B1302, Cl, Cl, OMe, F, 1-isopropyloxyhexyl), (B1303, Cl, Cl, OMe, F, 1-isopropyloxy-3,3-dimethylbutyl), (B1304, Cl, Cl, OMe, F, 1-isopropyloxyheptyl), (B1305, Cl, Cl, OMe, F, 1-isopropyloxyoctyl), (B1306, Cl, Cl, OMe, F, 1-isopropyloxynonyl), (B1307, Cl, Cl, OMe, F, 1-isopropyloxydecyl), (B1308, Cl, Cl, OMe, F, 1-isopropyloxyundecyl), (B1309, Cl, Cl, OMe, F, 1-isopropyloxydodecyl), (B1310, Cl, Cl, OMe, F, 1-isopropyloxy-1-cyclohexylmethyl), (B1311, Cl, Cl, OMe, F, 1-n-butyloxyethyl), (B1312, Cl, Cl, OMe, F, 1-n-butyloxypropyl), (B1313, Cl, Cl, OMe, F, 3-n-butyloxypropyl), (B1314, Cl, Cl, OMe, F, 1-n-butyloxybutyl), (B1315, Cl, Cl, OMe, F, 1,4-di(n-butyloxy)butyl), (B1316, Cl, Cl, OMe, F, 1-n-butyloxy-2-methylpropyl), (B1317, Cl, Cl, OMe, F, 1-n-butyloxypentyl), (B1318, Cl, Cl, OMe, F, 1-n-butyloxy-3-methylbutyl), (B1319, Cl, Cl, OMe, F, 1-n-butyloxy-2,2-dimethylpropyl), (B1320, Cl, Cl, OMe, F, 1-n-butyloxyhexyl), (B1321, Cl, Cl, OMe, F, 1-n-butyloxy-3,3-dimethylbutyl), (B1322, Cl, Cl, OMe, F, 1-n-butyloxyheptyl), (B1323, Cl, Cl, OMe, F, 1-n-butyloxyoctyl), (B1324, Cl, Cl, OMe, F, 1-n-butyloxynonyl), (B1325, Cl, Cl, OMe, F, 1-n-butyloxydecyl), (B1326, Cl, Cl, OMe, F, 1-n-butyloxyundecyl), (B1327, Cl, Cl, OMe, F, 1-n-butyloxydodecyl), (B1328, Cl, Cl, OMe, F, 1-n-butyloxy-1-cyclohexylmethyl), (B1329, Cl, Cl, OMe, F, 1-isobutyloxyethyl), (B1330, Cl, Cl, OMe, F, 1-isobutyloxypropyl), (B1331, Cl, Cl, OMe, F, 1-isobutyloxybutyl), (B1332, Cl, Cl, OMe, F, 1-isobutyloxy-2-methylpropyl), (B1333, Cl, Cl, OMe, F, 1-isobutyloxypentyl), (B1334, Cl, Cl, OMe, F, 1-isobutyloxy-3-methylbutyl), (B1335, Cl, Cl, OMe, F, 1-isobutyloxy-2,2-dimethylpropyl), (B1336, Cl, Cl, OMe, F, 1-isobutyloxyhexyl), (B1337, Cl, Cl, OMe, F, 1-isobutyloxy-3,3-dimethylbutyl), (B1338, Cl, Cl, OMe, F, 1-isobutyloxyheptyl), (B1339, Cl, Cl, OMe, F, 1-isobutyloxyoctyl), (B1340, Cl, Cl, OMe, F, 1-isobutyloxyynonyl), (B1341, Cl, Cl, OMe, F, 1-isobutyloxydecyl), (B1342, Cl, Cl, OMe, F, 1-isobutyloxyundecyl), (B1343, Cl, Cl, OMe, F, 1-isobutyloxydodecyl), (B1344, Cl, Cl, OMe, F, 1-isobutyloxy-1-cyclohexylmethyl), (B1345, Cl, Cl, OMe, F, 1-t-butyloxyethyl), (B1346, Cl, Cl, OMe, F, 1-t-butyloxypropyl), (B1347, Cl, Cl, OMe, F, 1-t-butyloxybutyl), (B1348, Cl, Cl, OMe, F, 1-t-butyloxy-2-methylpropyl), (B1349, Cl, Cl, OMe, F, 1-t-butyloxypentyl), (B1350, Cl, Cl, OMe, F, 1-t-butyloxy-3-methylbutyl), (B1351, Cl, Cl, OMe, F, 1-t-butyloxy-2,2-dimethylpropyl), (B1352, Cl, Cl, OMe, F, 1-t-butyloxyhexyl), (B1353, Cl, Cl, OMe, F, 1-t-butyloxy-3,3-dimethylbutyl), (B1354, Cl, Cl, OMe, F, 1-t-butyloxyheptyl), (B1355, Cl, Cl, OMe, F, 1-t-butyloxyoctyl), (B1356, Cl, Cl, OMe, F, 1-t-butyloxynonyl), (B1357, Cl, Cl, OMe, F, 1-t-butyloxydecyl), (B1358, Cl, Cl, OMe, F, 1-t-butyloxyundecyl), (B1359, Cl, Cl, OMe, F, 1-t-butyloxydodecyl), (B1360, Cl, Cl, OMe, F, 1-t-butyloxy-1-cyclohexylmethyl), (B1361, Cl, Cl, OMe, F, 1-n-pentyloxyethyl), (B1362, Cl, Cl, OMe, F, 1-n-pentyloxypropyl), (B1363, Cl, Cl, OMe, F, 3-n-pentyloxypropyl), (B1364, Cl, Cl, OMe, F, 1-n-pentyloxy-3-methylthiopropyl), (B1365, Cl, Cl, OMe, F, 1-n-pentyloxybutyl), (B1366, Cl, Cl, OMe, F, 1-n-pentyloxy-2-methylpropyl), (B1367, Cl, Cl, OMe, F, 1-n-pentyloxypentyl), (B1368, Cl, Cl, OMe, F, 1-n-pentyloxy-3-methylbutyl), (B1369, Cl, Cl, OMe, F, 1-n-pentyloxy-2,2-dimethylpropyl), (B1370, Cl, Cl, OMe, F, 1-n-pentyloxyhexyl), (B1371, Cl, Cl, OMe, F, 1-n-pentyloxy-3,3-dimethylbutyl), (B1372, Cl, Cl, OMe, F, 1-n-pentyloxyheptyl), (B1373, Cl, Cl, OMe, F, 1-n-pentyloxyoctyl), (B1374, Cl, Cl, OMe, F, 1-n-pentyloxynonyl), (B1375, Cl, Cl, OMe, F, 1-n-pentyloxydecyl), (B1376, Cl, Cl, OMe, F, 1-n-pentyloxyundecyl), (B1377, Cl, Cl, OMe, F, 1-n-pentyloxydodecyl), (B1378, Cl, Cl, OMe, F, 1-n-pentyloxy-1-cyclohexylmethyl), (B1379, Cl, Cl, OMe, F, 1-isopentyloxypropyl), (B1380, Cl, Cl, OMe, F, 1-neopentyloxyethyl), (B1381, Cl, Cl, OMe, F, 1-neopentyloxypropyl), (B1382, Cl, Cl, OMe, F, 3-neopentyloxypropyl), (B1383, Cl, Cl, OMe, F, 1-neopentyloxybutyl), (B1384, Cl, Cl, OMe, F, 1-neopentyloxy-2-methylpropyl), (B1385, Cl, Cl, OMe, F, 1-neopentyloxypentyl), (B1386, Cl, Cl, OMe, F, 1-neopentyloxy-3-methylbutyl), (B1387, Cl, Cl, OMe, F, 1-neopentyloxy-2,2-dimethylpropyl), (B1388, Cl, Cl, OMe, F, 1-neopentyloxyhexyl), (B1389, Cl, Cl, OMe, F, 1-neopentyloxy-3,3-dimethylbutyl), (B1390, Cl, Cl, OMe, F, 1-neopentyloxyheptyl), (B1391, Cl, Cl, OMe, F, 1-neopentyloxyoctyl), (B1392, Cl, Cl, OMe, F, 1-neopentyloxynonyl), (B1393, Cl, Cl, OMe, F, 1-neopentyloxydecyl), (B1394, Cl, Cl, OMe, F, 1-neopentyloxyundecyl), (B1395, Cl, Cl, OMe, F, 1-neopentyloxydodecyl), (B1396, Cl, Cl, OMe, F, 1-neopentyloxy-1-cyclohexylmethyl), (B 1397, Cl, Cl, OMe, F, 1-n-hexyloxyethyl), (B 1398, Cl, Cl, OMe, F, 1-n-hexyloxypropyl), (B1399, Cl, Cl, OMe, F, 3-n-hexyloxypropyl), (B1400, Cl, Cl, OMe, F, 1-n-hexyloxybutyl), (B1401, Cl, Cl, OMe, F, 1-n-hexyloxy-2-methylpropyl), (B1402, Cl, Cl, OMe, F, 1-n-hexyloxypentyl), (B1403, Cl, Cl, OMe, F, 1-n-hexyloxy-3-methylbutyl), (B1404, Cl, Cl, OMe, F, 1-n-hexyloxy-2,2-dimethylpropyl), (B1405, Cl, Cl, OMe, F, 1-n-hexyloxyhexyl), (B1406, Cl, Cl, OMe, F, 1-n-hexyloxy-3,3-dimethylbutyl), (B1407, Cl, Cl, OMe, F, 1-n-hexyloxyheptyl), (B1408, Cl, Cl, OMe, F, 1-n-hexyloxyoctyl), (B1409, Cl, Cl, OMe, F, 1-n-hexyloxynonyl), (B1410, Cl, Cl, OMe, F, 1-n-hexyloxydecyl), (B1411, Cl, Cl, OMe, F, 1-n-hexyloxyundecyl), (B1412, Cl, Cl, OMe, F, 1-n-hexyloxydodecyl), (B1413, Cl, Cl, OMe, F, 1-n-hexyloxy-1-cyclohexylmethyl), (B1414, Cl, Cl, OMe, F, 3-isohexyloxypropyl), (B1415, Cl, Cl, OMe, F, 3-(3,3-dimethylbutyloxy)propyl), (B1416, Cl, Cl, OMe, F, 3-(2-cyclopentyletoxy)propyl), (B1417, Cl, Cl, OMe, F, 1-n-octyloxyethyl), (B1418, Cl, Cl, OMe, OMe, 1-methyloxyethyl), (B1419, Cl, Cl, OMe, OMe, 1-methyloxypropyl), (B1420, Cl, Cl, OMe, OMe, 1-methyloxy-3-n-hexyloxypropyl), (B1421, Cl, Cl, OMe, OMe, 1-methyloxybutyl), (B1422, Cl, Cl, OMe, OMe, 1-methyloxy-4-n-pentyloxybutyl), (B 1423, Cl, Cl, OMe, OMe, 1-methyloxy-2-methylpropyl), (B 1424, Cl, Cl, OMe, OMe, 1-methyloxypentyl), (B1425, Cl, Cl, OMe, OMe, 1-methyloxy-3-methylbutyl), (B1426, Cl, Cl, OMe, OMe, 1-methyloxy-2,2-dimethylpropyl), (B1427, Cl, Cl, OMe, OMe, 1-methyloxyhexyl), (B1428, Cl, Cl, OMe, OMe, 4-methyloxyhexyl), (B1429, Cl, Cl, OMe, OMe, 1-methyloxy-4-methylpentyl), (B1430, Cl, Cl, OMe, OMe, 1-methyloxy-3,3-dimethylbutyl), (B1431, Cl, Cl, OMe, OMe, 3-methyloxy-2,4-dimethyl-3-pentyl), (B1432, Cl, Cl, OMe, OMe, 1-methyloxyheptyl), (B1433, Cl, Cl, OMe, OMe, 4-methyloxy-4-heptyl), (B1434, Cl, Cl, OMe, OMe, 1-methyloxyoctyl), (B1435, Cl, Cl, OMe, OMe, 3-methyloxyoctyl), (B1436, Cl, Cl, OMe, OMe, 1-methyloxynonyl), (B1437, Cl, Cl, OMe, OMe, 1-methyloxydecyl), (B1439, Cl, Cl, OMe, OMe, 1-methyloxydodecyl), (B1440, Cl, Cl, OMe, OMe, 1-methyloxy-1-cyclohexylmethyl), (B1441, Cl, Cl, OMe, OMe, 1-(4-ethyloxybutyloxy)-1-cyclohexylmethyl), (B 1442, Cl, Cl, OMe, OMe, 1-ethyloxyethyl), (B1443, Cl, Cl, OMe, OMe, 1-ethyloxypropyl), (B1444, Cl, Cl, OMe, OMe, 1-(4-ethyloxybutyloxy)propyl), (B1445, Cl, Cl, OMe, OMe, 1-ethyloxybutyl), (B1446, Cl, Cl, OMe, OMe, 1-ethyloxy-2-methylpropyl), (B1447, Cl, Cl, OMe, OMe, 1-ethyloxypentyl), (B1448, Cl, Cl, OMe, OMe, 1-ethyloxy-3-methylbutyl), (B1449, Cl, Cl, OMe, OMe, 1-ethyloxy-2,2-dimethylpropyl), (B1450, Cl, Cl, OMe, OMe, 1-ethyloxyhexyl), (B1451, Cl, Cl, OMe, OMe, 1-ethyloxy-3,3-dimethylbutyl), (B1452, Cl, Cl, OMe, OMe, 1-ethyloxyheptyl), (B1453, Cl, Cl, OMe, OMe, 1-ethyloxyoctyl), (B1454, Cl, Cl, OMe, OMe, 1-ethyloxynonyl), (B1455, Cl, Cl, OMe, OMe, 1-ethyloxydecyl), (B1456, Cl, Cl, OMe, OMe, 1-ethyloxyundecyl), (B1457, Cl, Cl, OMe, OMe, 1-ethyloxydodecyl), (B 1458, Cl, Cl, OMe, OMe, 1-ethyloxy-1-cyclohexylmethyl), (B1459, Cl, Cl, OMe, OMe, 1-n-propyloxyethyl), (B1460, Cl, Cl, OMe, OMe, 1-n-propyloxypropyl), (B1461, Cl, Cl, OMe, OMe, 3-n-propyloxypropyl), (B1462, Cl, Cl, OMe, OMe, 1-n-propyloxybutyl), (B1463, Cl, Cl, OMe, OMe, 1,4-di(n-propyloxy)butyl), (B1464, Cl, Cl, OMe, OMe, 1-n-propyloxy-2-methylpropyl), (B1465, Cl, Cl, OMe, OMe, 1-n-propyloxypentyl), (B1466, Cl, Cl, OMe, OMe, 1-n-propyloxy-3-methylbutyl), (B1467, Cl, Cl, OMe, OMe, 1-n-propyloxy-2,2-dimethylpropyl), (B1468, Cl, Cl, OMe, OMe, 1-n-propyloxyhexyl), (B1469, Cl, Cl, OMe, OMe, 1-n-propyloxy-3,3-dimethylbutyl), (B1470, Cl, Cl, OMe, OMe, 1-n-propyloxyheptyl), (B1471, Cl, Cl, OMe, OMe, 1-n-propyloxyoctyl), (B1472, Cl, Cl, OMe, OMe, 1-n-propyloxynonyl), (B1473, Cl, Cl, OMe, OMe, 1-n-propyloxydecyl), (B1474, Cl, Cl, OMe, OMe, 1-n-propyloxyundecyl), (B 1475, Cl, Cl, OMe, OMe, 1-n-propyloxydodecyl), (B1476, Cl, Cl, OMe, OMe, 1-n-propyloxy-1-cyclohexylmethyl), (B1477, Cl, Cl, OMe, OMe, 1-isopropyloxyethyl), (B1478, Cl, Cl, OMe, OMe, 1-isopropyloxypropyl), (B1479, Cl, Cl, OMe, OMe, 3-isopropyloxypropyl), (B1480, Cl, Cl, OMe, OMe, 1-isopropyloxybutyl), (B1481, Cl, Cl, OMe, OMe, 1-isopropyloxy-2-methylpropyl), (B1482, Cl, Cl, OMe, OMe, 1-isopropyloxypentyl), (B1483, Cl, Cl, OMe, OMe, 1-isopropyloxy-3-methylbutyl), (B 1484, Cl, Cl, OMe, OMe, 1-isopropyloxy-2,2-dimethylpropyl), (B1485, Cl, Cl, OMe, OMe, 1-isopropyloxyhexyl), (B1486, Cl, Cl, OMe, OMe, 1-isopropyloxy-3,3-dimethylbutyl), (B1487, Cl, Cl, OMe, OMe, 1-isopropyloxyheptyl), (B1488, Cl, Cl, OMe, OMe, 1-isopropyloxyoctyl), (B1489, Cl, Cl, OMe, OMe, 1-isopropyloxynonyl), (B1490, Cl, Cl, OMe, OMe, 1-isopropyloxydecyl), (B1491, Cl, Cl, OMe, OMe, 1-isopropyloxyundecyl), (B1492, Cl, Cl, OMe, OMe, 1-isopropyloxydodecyl), (B1493, Cl, Cl, OMe, OMe, 1-isopropyloxy-1-cyclohexylmethyl), (B1494, Cl, Cl, OMe, OMe, 1-n-butyloxyethyl), (B1495, Cl, Cl, OMe, OMe, 1-n-butyloxypropyl), (B1496, Cl, Cl, OMe, OMe, 3-n-butyloxypropyl), (B1497, Cl, Cl, OMe, OMe, 1-n-butyloxybutyl), (B1498, Cl, Cl, OMe, OMe, 1,4-di(n-butyloxy)butyl), (B1499, Cl, Cl, OMe, OMe, 1-n-butyloxy-2-methylpropyl), (B1500, Cl, Cl, OMe, OMe, 1-n-butyloxypentyl), (B1501, Cl, Cl, OMe, OMe, 1-n-butyloxy-3-methylbutyl), (B1502, Cl, Cl, OMe, OMe, 1-n-butyloxy-2,2-dimethylpropyl), (B1503, Cl, Cl, OMe, OMe, 1-n-butyloxyhexyl), (B1504, Cl, Cl, OMe, OMe, 1-n-butyloxy-3,3-dimethylbutyl), (B1505, Cl, Cl, OMe, OMe, 1-n-butyloxyheptyl), (B1506, Cl, Cl, OMe, OMe, 1-n-butyloxyoctyl), (B1507, Cl, Cl, OMe, OMe, 1-n-butyloxynonyl), (B1508, Cl, Cl, OMe, OMe, 1-n-butyloxydecyl), (B1509, Cl, Cl, OMe, OMe, 1-n-butyloxyundecyl), (B1510, Cl, Cl, OMe, OMe, 1-n-butyloxydodecyl), (B1511, Cl, Cl, OMe, OMe, 1-n-butyloxy-1-cyclohexylmethyl), (B1512, Cl, Cl, OMe, OMe, 1-isobutyloxyethyl), (B1513, Cl, Cl, OMe, OMe, 1-isobutyloxypropyl), (B1514, Cl, Cl, OMe, OMe, 1-isobutyloxybutyl), (B1515, Cl, Cl, OMe, OMe, 1-isobutyloxy-2-methylpropyl), (B1516, Cl, Cl, OMe, OMe, 1-isobutyloxypentyl), (B 1517, Cl, Cl, OMe, OMe, 1-isobutyloxy-3-methylbutyl), (B 1518, Cl, Cl, OMe, OMe, 1-isobutyloxy-2,2-dimethylpropyl), (B1519, Cl, Cl, OMe, OMe, 1-isobutyloxyhexyl), (B1520, Cl, Cl, OMe, OMe, 1-isobutyloxy-3,3-dimethylbutyl), (B1521, Cl, Cl, OMe, OMe, 1-isobutyloxyheptyl), (B1522, Cl, Cl, OMe, OMe, 1-isobutyloxyoctyl), (B1523, Cl, Cl, OMe, OMe, 1-isobutyloxyynonyl), (B1524, Cl, Cl, OMe, OMe, 1-isobutyloxydecyl), (B1525, Cl, Cl, OMe, OMe, 1-isobutyloxyundecyl), (B1526, Cl, Cl, OMe, OMe, 1-isobutyloxydodecyl), (B1527, Cl, Cl, OMe, OMe, 1-isobutyloxy-1-cyclohexylmethyl), (B1528, Cl, Cl, OMe, OMe, 1-t-butyloxyethyl), (B1529, Cl, Cl, OMe, OMe, 1-t-butyloxypropyl), (B1530, Cl, Cl, OMe, OMe, 1-t-butyloxybutyl), (B1531, Cl, Cl, OMe, OMe, 1-t-butyloxy-2-methylpropyl), (B1532, Cl, Cl, OMe, OMe, 1-t-butyloxypentyl), (B1533, Cl, Cl, OMe, OMe, 1-t-butyloxy-3-methylbutyl), (B1534, Cl, Cl, OMe, OMe, 1-t-butyloxy-2,2-dimethylpropyl), (B1535, Cl, Cl, OMe, OMe, 1-t-butyloxyhexyl), (B1536, Cl, Cl, OMe, OMe, 1-t-butyloxy-3,3-dimethylbutyl), (B1537, Cl, Cl, OMe, OMe, 1-t-butyloxyheptyl), (B1538, Cl, Cl, OMe, OMe, 1-t-butyloxyoctyl), (B1539, Cl, Cl, OMe, OMe, 1-t-butyloxynonyl), (B1540, Cl, Cl, OMe, OMe, 1-t-butyloxydecyl), (B1541, Cl, Cl, OMe, OMe, 1-t-butyloxyundecyl), (B1542, Cl, Cl, OMe, OMe, 1-t-butyloxydodecyl), (B1543, Cl, Cl, OMe, OMe, 1-t-butyloxy-1-cyclohexylmethyl), (B1544, Cl, Cl, OMe, OMe, 1-n-pentyloxyethyl), (B1545, Cl, Cl, OMe, OMe, 1-n-pentyloxypropyl), (B1546, Cl, Cl, OMe, OMe, 3-n-pentyloxypropyl), (B1547, Cl, Cl, OMe, OMe, 1-n-pentyloxy-3-methylthiopropyl), (B1548, Cl, Cl, OMe, OMe, 1-n-pentyloxybutyl), (B1549, Cl, Cl, OMe, OMe, 1-n-pentyloxy-2-methylpropyl), (B1550, Cl, Cl, OMe, OMe, 1-n-pentyloxypentyl), (B1551, Cl, Cl, OMe, OMe, 1-n-pentyloxy-3-methylbutyl), (B1552, Cl, Cl, OMe, OMe, 1-n-pentyloxy-2,2-dimethylpropyl), (B1553, Cl, Cl, OMe, OMe, 1-n-pentyloxyhexyl), (B1554, Cl, Cl, OMe, OMe, 1-n-pentyloxy-3,3-dimethylbutyl), (B1555, Cl, Cl, OMe, OMe, 1-n-pentyloxyheptyl), (B1556, Cl, Cl, OMe, OMe, 1-n-pentyloxyoctyl), (B1557, Cl, Cl, OMe, OMe, 1-n-pentyloxynonyl), (B1558, Cl, Cl, OMe, OMe, 1-n-pentyloxydecyl), (B1559, Cl, Cl, OMe, OMe, 1-n-pentyloxyundecyl), (B1560, Cl, Cl, OMe, OMe, 1-n-pentyloxydodecyl), (B1561, Cl, Cl, OMe, OMe, 1-n-pentyloxy-1-cyclohexylmethyl), (B1562, Cl, Cl, OMe, OMe, 1-isopentyloxypropyl), (B1563, Cl, Cl, OMe, OMe, 1-neopentyloxyethyl), (B1564, Cl, Cl, OMe, OMe, 1-neopentyloxypropyl), (B1565, Cl, Cl, OMe, OMe, 3-neopentyloxypropyl), (B1566, Cl, Cl, OMe, OMe, 1-neopentyloxybutyl), (B1567, Cl, Cl, OMe, OMe, 1-neopentyloxy-2-methylpropyl), (B1568, Cl, Cl, OMe, OMe, 1-neopentyloxypentyl), (B1569, Cl, Cl, OMe, OMe, 1-neopentyloxy-3-methylbutyl), (B1570, Cl, Cl, OMe, OMe, 1-neopentyloxy-2,2-dimethylpropyl), (B1571, Cl, Cl, OMe, OMe, 1-neopentyloxyhexyl), (B1572, Cl, Cl, OMe, OMe, 1-neopentyloxy-3,3-dimethylbutyl), (B1573, Cl, Cl, OMe, OMe, 1-neopentyloxyheptyl), (B1574, Cl, Cl, OMe, OMe, 1-neopentyloxyoctyl), (B1575, Cl, Cl, OMe, OMe, 1-neopentyloxynonyl), (B1576, Cl, Cl, OMe, OMe, 1-neopentyloxydecyl), (B1577, Cl, Cl, OMe, OMe, 1-neopentyloxyundecyl), (B1578, Cl, Cl, OMe, OMe, 1-neopentyloxydodecyl), (B1579, Cl, Cl, OMe, OMe, 1-neopentyloxy-1-cyclohexylmethyl), (B1580, Cl, Cl, OMe, OMe, 1-n-hexyloxyethyl), (B1581, Cl, Cl, OMe, OMe, 1-n-hexyloxypropyl), (B1582, Cl, Cl, OMe, OMe, 3-n-hexyloxypropyl), (B1583, Cl, Cl, OMe, OMe, 1-n-hexyloxybutyl), (B1584, Cl, Cl, OMe, OMe, 1-n-hexyloxy-2-methylpropyl), (B1585, Cl, Cl, OMe, OMe, 1-n-hexyloxypentyl), (B1586, Cl, Cl, OMe, OMe, 1-n-hexyloxy-3-methylbutyl), (B1587, Cl, Cl, OMe, OMe, 1-n-hexyloxy-2,2-dimethylpropyl), (B1588, Cl, Cl, OMe, OMe, 1-n-hexyloxyhexyl), (B1589, Cl, Cl, OMe, OMe, 1-n-hexyloxy-3,3-dimethylbutyl), (B1590, Cl, Cl, OMe, OMe, 1-n-hexyloxyheptyl), (B1591, Cl, Cl, OMe, OMe, 1-n-hexyloxyoctyl), (B1592, Cl, Cl, OMe, OMe, 1-n-hexyloxynonyl), (B1593, Cl, Cl, OMe, OMe, 1-n-hexyloxydecyl), (B1594, Cl, Cl, OMe, OMe, 1-n-hexyloxyundecyl), (B1595, Cl, Cl, OMe, OMe, 1-n-hexyloxydodecyl), (B1596, Cl, Cl, OMe, OMe, 1-n-hexyloxy-1-cyclohexylmethyl), (B1597, Cl, Cl, OMe, OMe, 3-isohexyloxypropyl), (B1598, Cl, Cl, OMe, OMe, 3-(3,3-dimethylbutyloxy)propyl), (B1599, Cl, Cl, OMe, OMe, 3-(2-cyclopentylethyloxy)propyl), (B1600, Cl, Cl, OMe, OMe, 1-n-octyloxyethyl), (B1601, F, F, F, F, 1-methyloxy-3-n-hexyloxypropyl), (B1602, F, F, Cl, F, 1-methyloxy-3-n-hexyloxypropyl), (B1603, F, F, F, F, 1-methyloxy-4-n-pentyloxybutyl), (B1604, F, F, Cl, F, 1-methyloxy-4-n-pentyloxybutyl), (B1605, F, F, Me, F, 1-methyloxy-2,2-dimethylpropyl), (B1606, F, F, Me, F, 1-methyloxy-4-methylpentyl), (B1607, F, F, Me, F, 1-methyloxyheptyl), (B1608, F, F, Me, F, 1-methyloxyoctyl), (B1609, F, F, Me, F, 1-methyloxynonyl), (B1610, F, F, Me, F, 1-methyloxydecyl), (B1611, F, F, Me, F, 1-(4-ethyloxybutyloxy)-1-cyclohexylmethyl), (B 1612, F, F, Me, F, 1-(4-ethyloxybutyloxy)propyl), (B1613, F, F, Me, F, 1-ethyloxypentyl), (B1614, F, F, Me, F, 1-n-propyloxybutyl), (B1615, F, F, Me, F, 1-n-propyloxypentyl), (B1616, F, F, Me, F, 1-n-butyloxyethyl), (B1617, F, F, Me, F, 1-n-butyloxypropyl), (B1618, F, F, Me, F, 3-n-butyloxypropyl), (B1619, F, F, Me, F, 1-n-butyloxybutyl), (B1620, F, F, Me, F, 1,4-di(n-butyloxy)butyl), (B1621, F, F, Me, F, 1-n-butyloxypentyl), (B1622, F, F, Me, F, 1-n-pentyloxyethyl), (B1623, F, F, Me, F, 1-n-pentyloxypropyl), (B1624, F, F, Me, F, 3-n-pentyloxypropyl), (B1625, F, F, Me, F, 1-n-pentyloxy-3-methylthiopropyl), (B1626, F, F, Me, F, 1-n-pentyloxybutyl), (B1627, F, F, Me, F, 1-n-pentyloxypentyl), (B1628, F, F, Me, F, 1-n-pentyloxy-2,2-dimethylpropyl), (B1629, F, F, Me, F, 1-n-pentyloxy-1-cyclohexylmethyl), (B1630, F, F, Me, F, 1-isopentyloxypropyl), (B1631, F, F, Me, F, 3-neopentyloxypropyl), (B1632, F, F, Me, F, 1-n-hexyloxypropyl), (B1633, F, F, Me, F, 3-n-hexyloxypropyl), (B1634, F, F, Me, F, 3-isohexyloxypropyl), (B1635, F, F, Me, F, 3-(3,3-dimethylbutyloxy)propyl), (B1636, F, F, Me, F, 3-(2-cyclopentylethyloxy)propyl), (B1637, F, F, Me, F, 1-n-octyloxyethyl), (B1638, Cl, Cl, Me, F, 1-methyloxy-2,2-dimethylpropyl), (B1639, Cl, Cl, Me, F, 1-methyloxyhexyl), (B1640, Cl, Cl, Me, F, 1-methyloxy-4-methylpentyl), (B1641, Cl, Cl, Me, F, 1-methyloxyheptyl), (B1642, Cl, Cl, Me, F, 1-methyloxyoctyl), (B1643, Cl, Cl, Me, F, 3-methyloxyoctyl), (B1644, Cl, Cl, Me, F, 1-methyloxynonyl), (B1645, Cl, Cl, Me, F, 1-methyloxydecyl), (B1646, Cl, Cl, Me, F, 1-methyloxyundecyl), (B1647, Cl, Cl, Me, F, 1-(4-ethyloxybutyloxy)propyl), (B1648, Cl, Cl, Me, F, 1-ethyloxypentyl), (B1649, Cl, Cl, Me, F, 1-ethyloxy-3,3-dimethylbutyl), (B1650, Cl, Cl, Me, F, 1-n-propyloxyethyl), (B1651, Cl, Cl, Me, F, 1-n-propyloxypropyl), (B1652, Cl, Cl, Me, F, 3-n-propyloxypropyl), (B1653, Cl, Cl, Me, F, 1-n-propyloxybutyl), (B1654, Cl, Cl, Me, F, 1,4-di(n-propyloxy)butyl), (B1655, Cl, Cl, Me, F, 1-n-propyloxypentyl), (B1656, Cl, Cl, Me, F, 3-isopropyloxypropyl), (B1657, Cl, Cl, Me, F, 1-n-butyloxyethyl), (B1658, Cl, Cl, Me, F, 1-n-butyloxypropyl), (B1659, Cl, Cl, Me, F, 3-n-butyloxypropyl), (B1660, Cl, Cl, Me, F, 1-n-butyloxybutyl), (B1661, Cl, Cl, Me, F, 1-n-butyloxypentyl), (B1662, Cl, Cl, Me, F, 1-n-pentyloxypropyl), (B1663, Cl, Cl, Me, F, 3-n-pentyloxypropyl), (B1664, Cl, Cl, Me, F, 1-n-pentyloxy-3-methylthiopropyl), (B1665, Cl, Cl, Me, F, 1-n-pentyloxybutyl), (B1666, Cl, Cl, Me, F, 1-n-pentyloxypentyl), (B1667, Cl, Cl, Me, F, 1-isopentyloxypropyl), (B1668, Cl, Cl, Me, F, 3-neopentyloxypropyl), (B1669, Cl, Cl, Me, F, 1-n-hexyloxypropyl), (B1670, Cl, Cl, Me, F, 3-n-hexyloxypropyl), (B1671, Cl, Cl, Me, F, 3-isohexyloxypropyl), (B1672, Cl, Cl, Me, F, 3-(3,3-dimethylbutyloxy)propyl), (B1673, Cl, Cl, Me, F, 3-(2-cyclopentylethyloxy)propyl), (B1674, Cl, Cl, Me, F, 1-n-octyloxyethyl), (B1675, Me, Me, Me, F, 1-methyloxy-3-n-hexyloxypropyl), (B1676, Me, Me, Me, F, 1-methyloxy-4-n-pentyloxybutyl), (B1677, Me, Me, Me, F, 1-methyloxy-2,2-dimethylpropyl), (B1678, Me, Me, Me, F, 1-methyloxyhexyl), (B1679, Me, Me, Me, F, 1-methyloxy-4-methylpentyl), (B1680, Me, Me, Me, F, 1-methyloxyheptyl), (B1681, Me, Me, Me, F, 1-methyloxyoctyl), (B1682, Me, Me, Me, F, 3-methyloxyoctyl), (B1683, Me, Me, Me, F, 1-methyloxynonyl), (B1684, Me, Me, Me, F, 1-methyloxydecyl), (B1685, Me, Me, Me, F, 1-methyloxyundecyl), (B1686, Me, Me, Me, F, 1-(4-ethyloxybutyloxy)-1-cyclohexylmethyl), (B1687, Me, Me, Me, F, 1-(4-ethyloxybutyloxy)propyl), (B1688, Me, Me, Me, F, 1-ethyloxypentyl), (B1689, Me, Me, Me, F, 1-ethyloxy-3,3-dimethylbutyl), (B1690, Me, Me, Me, F, 1-n-propyloxyethyl), (B1691, Me, Me, Me, F, 1-n-propyloxypropyl), (B1692, Me, Me, Me, F, 3-n-propyloxypropyl), (B1693, Me, Me, Me, F, 1-n-propyloxybutyl), (B1694, Me, Me, Me, F, 1,4-di(n-propyloxy)butyl), (B1695, Me, Me, Me, F, 1-n-propyloxypentyl), (B1696, Me, Me, Me, F, 3-isopropyloxypropyl), (B1697, Me, Me, Me, F, 1-n-butyloxyethyl), (B1698, Me, Me, Me, F, 1-n-butyloxypropyl), (B1699, Me, Me, Me, F, 3-n-butyloxypropyl), (B1700, Me, Me, Me, F, 1-n-butyloxybutyl), (B1701, Me, Me, Me, F, 1,4-di(n-butyloxy)butyl), (B1702, Me, Me, Me, F, 1-n-butyloxypentyl), (B1703, Me, Me, Me, F, 1-n-pentyloxyethyl), (B1704, Me, Me, Me, F, 1-n-pentyloxypropyl), (B1705, Me, Me, Me, F, 3-n-pentyloxypropyl), (B1706, Me, Me, Me, F, 1-n-pentyloxy-3-methylthiopropyl), (B1707, Me, Me, Me, F, 1-n-pentyloxybutyl), (B1708, Me, Me, Me, F, 1-n-pentyloxypentyl), (B1709, Me, Me, Me, F, 1-n-pentyloxy-2,2-dimethylpropyl), (B1710, Me, Me, Me, F, 1-n-pentyloxy-1-cyclohexylmethyl), (B1711, Me, Me, Me, F, 1-isopentyloxypropyl), (B1712, Me, Me, Me, F, 3-neopentyloxypropyl), (B1713, Me, Me, Me, F, 1-n-hexyloxypropyl), (B1714, Me, Me, Me, F, 3-n-hexyloxypropyl), (B1715, Me, Me, Me, F, 3-isohexyloxypropyl), (B1716, Me, Me, Me, F, 3-(3,3-dimethylbutyloxy)propyl), (B1717, Me, Me, Me, F, 3-(2-cyclopentylethyloxy)propyl), (B1718, Me, Me, Me, F, 1-n-octyloxyethyl), (B1719, Me, Me, Me, F, 1-methyloxyhexyl), (B1720, Me, Me, Me, F, 3-methyloxyoctyl), (B1721, Me, Me, Me, F, 1-methyloxyundecyl), (B1722, Me, Me, Me, F, 1-ethyloxy-3,3-dimethylbutyl), (B1723, Me, Me, Me, F, 1-n-propyloxyethyl), (B1724, Me, Me, Me, F, 1-n-propyloxypropyl), (B1725, Me, Me, Me, F, 3-n-propyloxypropyl), (B1726, Me, Me, Me, F, 1,4-di(n-propyloxy)butyl), (B1727, Me, Me, Me, F, 3-isopropyloxypropyl)

Example 584
Synthesis of 3-(4-{4-[3-(1-n-butyloxypropyl)-2-fluorophenyl]thiazol-2-ylcarbonyl}-2,6-difluorophenyl)-2-methylacrylic acid disodium salt (C1)

To a suspension of methanol (100 mL) solution of 3-(4-{4-[3-(1-n-butyloxypropyl)-2-fluorophenyl]thiazol-2-ylcarbonyl}-2,6-difluorophenyl)-2-methylacrylic acid (3.22 mg) was added 2M sodium hydroxide aqueous solution (6.06 mL). After stirring for 1 h, n-hexylaldehyde (5.88 mL) was added to the reaction mixture. After methanol was evaporated under reduced pressure, the obtained residue was redissolved by adding water (40 mL). The water solution was freeze drying to obtain the compound (C1) 3.40 g.

¹H-NMR(DMSO-d6) 8.05-8.11 (m, 1H), 7.69-7.75 (m, 1H), 7.22-7.29 (m, 2H), 7.15 (d, 1H, J=3.1 Hz), 7.03 (s, 1H), 4.56-4.60 (m, 1H), 3.31 (t, 2H, J=6.3 Hz), 1.65-1.80 (m, 5H), 1.45-1.55 (m, 2H), 1.30-1.40 (m, 2H), 0.83-0.91 (m, 6H).

C2 to C6 were synthesized by similar metod described above.

Example 585
Synthesis of 3-[2,6-dichloro-4-(4-{3-[3-(2-ethylbutyloxy)propyl]-2-fluorophenyl}thiazol-2-ylcarbonyl)phenyl]-2-methylacrylic acid disodium salt (C2)

1H-NMR(DMSO-d6) 8.11 (s, 2H), 7.97-8.03 (m, 2H), 7.11-7.18 (m, 1H), 3.26-3.41 (m, 4H), 2.72 (t, 2H, J=7.3 Hz), 1.78-1.87 (m, 2H), 1.62 (s, 3H), 1.24-1.62 (m, 5H), 0.86 (t, 6H, J=7.3 Hz).

Example 586
Synthesis of 3-(2,6-dichloro-4-{4-[2-fluoro-3-(1-methyloxydecyl)phenyl]thiazol-2-ylcarbonyl}phenyl)-2-methylacrylic acid disodium salt (C3)

1H-NMR(DMSO-d6) 8.06-8.17 (m, 3H), 7.20-7.28 (m, 2H), 7.13 (d, 1H, J=3.2 Hz), 7.06 (s, 1H), 4.53-4.58 (m, 1H), 3.17 (s, 3H), 1.60-1.82 (m, 5H), 1.23 (m, 14H), 0.86 (t, 3H, J=7.0 Hz).

Example 587
Synthesis of 3-(2,6-dichloro-4-{4-[2-fluoro-3-(1-methyloxyoctyl)phenyl]thiazol-2-ylcarbonyl}phenyl)-2-methylacrylic acid disodium salt (C4)

1H-NMR(DMSO-d6) 8.06-8.12 (m, 3H), 7.23-7.29 (m, 2H), 7.16 (d, 1H, J=3.1 Hz), 7.12 (s, 1H), 4.53-4.57 (m, 1H), 3.17 (s, 3H), 1.60-1.82 (m, 5H), 1.23-1.37 (m, 10H), 0.84 (t, 3H, J=6.6 Hz).

Example 588
Synthesis of 3-(2,6-dichloro-4-{4-[2-fluoro-3-(3-n-propyloxypropyl)phenyl]thiazol-2-ylcarbonyl}phenyl)-2-methylacrylic acid disodium salt (C5)

1H-NMR(DMSO-d6) 8.13 (s, 2H), 7.98-8.04 (m, 1H), 7.12-7.17 (m, 4H), 3.40 (t, 2H, J=6.3 Hz), 3.30 (t, 2H, J=6.6 Hz), 7.20 (t, 2H, J=7.5 Hz), 1.78-1.88 (m, 2H), 1.64 (s, 3H), 1.47-1.64 (m, 2H), 0.88 (t, 3H, J=7.5 Hz).

Example 589
Synthesis of 3-(4-{4-[3-(3-ethyloxypropyl)-2-fluorophenyl]thiazol-2-ylcarbonyl}-2,6-difluorophenyl)-2-methylacrylic acid disodium salt (C6)

1H-NMR(DMSO-d6) 7.99-8.05 (m, 1H), 7.72-7.78 (m, 2H), 7.12-7.19 (m, 3H), 7.07 (s, 1H), 3.38-3.47 (m, 4H), 2.69-2.74 (m, 2H), 1.76-1.87 (m, 5H), 1.13 (t, 3H, J=7.0 Hz).

Test Examples
Test Example 1
Isolation and Purification of Thrombopoietin (TPO)

Human TPO (hTPO) and murine TPO (mTPO) were purchased from R&D Systems.

Test Example 2
The Thrombopoietic Activity

The TPO dependent BaF/hTPOR cell line which was established by introducing human TPO receptor (hTPOR) into BaF-B03 cells according to Collins et al (J. Cell. Physiol., 137:293-298 (1988)) was used to test the thrombopoietic activity of the present compound. The DNA sequences and encoded peptide sequences for human hTPOR have been described by Vigon et al (Proc. Natl. Acad. Sci. USA, 89:5640-5644 (1992)). TPO dose not have any ability to support proliferation of interlukin-3 dependent parental cell line BaF-B03. BAF/hTPOR cells were maintained in RPMI medium and WEHI-3B conditioned medium as a source of murine interleukin-3 (IL-3). These cells were washed and resuspended in RPMI medium without a source of murine IL-3 and seeded into each well of 96-well microtiter plates at a density of 5×10⁴cells per well in the absence or presence of various concentration of hTPO or the present compound. After incubation at 37° C. for 20 hours in the 5% CO₂incubator, 10% WST-1 reagent (Takara Biomedicals, Japan) was added to each wells and the cells were further incubated for 4 hours. The absorbance at 450 nm was measured. Tables 1 and 2 exemplify the ED₅₀for tested compounds of the present invention, wherein the ED₅₀is the half concentration of the concentration showing the maximum thrombopoietic activity.

TABLE 1No.ED50(μM)A10.00227A20.004A30.004A40.00180A50.00191A60.00104A70.00226A80.0029A90.0030A100.0012A110.00087A120.0008A11230.00727A13080.0129A13090.01278A13100.0123A13110.00886A13120.01083A13140.01251A13150.01247A13160.00529A13170.01506B10.0022B20.004B60.0024B70.0036B80.0040B90.0016B100.0019B110.00081B120.0021B130.0010B140.00073B150.00073B160.00077B180.00057B190.00073B200.00081B210.00067B220.00114B230.00123B240.00197B250.00093B260.00039B270.00075B280.00079B290.00203B300.00078B310.00085B320.00303B330.00333B340.00099B350.00077B360.00063B370.00088B380.00062B390.00101B400.00088B410.00067B420.00034B430.00165B440.00127B450.00136B460.00128B470.00280B480.00223B490.0013B500.00080B510.00068B520.0017B530.0014B560.0027B580.0015B600.00075B610.00076B620.00076B630.00020B640.00119B650.00104B660.00091B670.00048B680.00082B690.00078B700.00043B710.00100B720.00078B730.00135B740.00080B750.00077B760.00298B770.00306B780.00097B790.00077B800.00070B810.00139B820.00107B830.00072B840.00102B850.00088B860.00063B870.00062B880.00311B890.00151B900.00115B910.00102B930.00091B940.00097B950.00082B960.00078B970.00094B980.00073B990.00059B1000.00068B1010.0019B3470.01872B3490.01679B3540.0032B3550.0033B3800.02325B3970.00252B4180.0063B4190.01455B4250.00201B4840.00129B4880.01588B5050.012B5190.00103B5210.01688B10540.01994B10590.0032B10600.0039B11020.00286B11220.00825B11240.01584B14370.0065B14380.0063B17990.01732B18000.00304B18330.01899B18480.01594B18510.01684B18520.01648B18770.01304B18840.01685B18900.01815B18920.01164B19160.01286B19200.01452B19220.01359B19250.01841B19260.01556B19270.01944B19280.01257B19330.00788B19340.01304B19360.01711B19380.01268B19400.01883B19450.01927B19480.01091B19490.01316B19520.01013B19530.01007B19540.01294B19550.01165B19560.01507B19570.01275B19580.00757B19590.01126B19600.01014B19900.01214B19910.01323B19920.01305B19930.01392B19940.01424B19950.01093B19970.01553B19980.00835B19990.01324B20010.01942B20040.01394B20050.01033B20200.01094B20210.00609B20220.01563B20230.00645B20240.00996B20250.0032B20260.01259B20270.01259B20280.01143B20990.00291

TABLE 2

No.
ED50(μM)

B380
0.02325

B1836
0.02102

B1849
0.02245

B1854
0.02443

B1855
0.02133

B1861
0.02282

B1863
0.02276

B1878
0.02119

B1886
0.02208

B1900
0.02316

B1901
0.02425

B1904
0.02457

B1905
0.02665

B1908
0.02628

B1909
0.02586

B1918
0.02102

B1919
0.02793

B1923
0.02017

B1924
0.02058

B1929
0.02584

B1935
0.0254

B1937
0.02308

B1941
0.02413

B1951
0.02226

B1963
0.02858

B2000
0.0205

B2003
0.02271

B2012
0.02419

B2018
0.02351

Formulation Example
Formulation Example 1

Granules are prepared using the following ingredients.

IngredientsThe compound10mgrepresented by the formula (I)Lactose700mgCorn starch274mgHPC-L16mg1000mg

The compound represented by the formula (I) and lactose are made pass through a 60 mesh sieve. Corn starch is made pass through a 120 mesh sieve. They are mixed by a twin shell blender. An aqueous solution of HPC-L (low mucosity hydroxypropylcellulose) is added to the mixture and the resulting mixture is kneaded, granulated (by the extrusion with pore size 0.5 to 1 mm mesh), and dried. The dried granules thus obtained are sieved by a swing sieve (12/60 mesh) to yield the granules.

Formulation 2

Powders for filling capsules are prepared using the following ingredients.

IngredientsThe compound10mgrepresented by the formula (I)Lactose79mgCorn starch10mgMagnesium stearate1mg100mg

The compound represented by the formula (I) and lactose are made pass through a 60 mesh sieve. Corn starch is made pass through a 120 mesh sieve. These ingredients and magnesium stearate are mixed by a twin shell blender. 100 mg of the 10-fold trituration is filled into a No. 5 hard gelatin capsule.

Formulation 3

Granules for filling capsules are prepared using the following ingredients.

IngredientsThe compound15mgrepresented by the formula (I)Lactose90mgCorn starch42mgHPC-L3mg150mg

The compound represented by the formula (I) and lactose are made pass through a 60 mesh sieve. Corn starch is made pass through a 120 mesh sieve. After mixing them, an aqueous solution of HPC-L is added to the mixture and the resulting mixture is kneaded, granulated, and dried. After the dried granules are lubricated, 150 mg of that are filled into a No. 4 hard gelatin capsule.

Formulation 4

Tablets are prepared using the following ingredients.

IngredientsThe compound10mgrepresented by the formula (I)Lactose90mgMicrocrystal cellulose30mgCMC-Na15mgMagnesium stearate5mg150mg

The compound represented by the formula (I), lactose, microcrystal cellulose, and CMC-Na (carboxymethylcellulose sodium salt) are made pass through a 60 mesh sieve and then mixed. The resulting mixture is mixed with magnesium stearate to obtain the mixed powder for the tablet formulation. The mixed powder is compressed to yield tablets of 150 mg.

Formulation 5

Intravenous formulations are prepared using the following ingredients.

IngredientsThe compound represented by the formula (I)100mgSaturated fattyacid glyceride1000ml

Usually a solution of ingredients above described is administered intravenously to a patient by the speed of 1 ml/min.

INDUSTRIAL APPLICABILITY

The compounds of the present invention have thrombopoietin receptor agonism and are useful as the treating or preventing agent for hemopathy accompanied with unusual count of platelet, for example, thrombocytopenia and the like

Compounds exhibiting thrombopoietin receptor agonism

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