Alkylene derivatives

Abstract

The object of the present invention is to provide novel compounds having ACC2 inhibiting activity. In addition, the object of the present invention is to provide a pharmaceutical composition comprising the compound. A compound of formula (I): ##STR00001## wherein R.sup.1 is substituted or unsubstituted fused aromatic heterocyclyl etc., ring A is substituted or unsubstituted non-aromatic carbocycle etc., -L.sup.1- is O(CR.sup.6R.sup.7)m- etc., -L.sup.2- is O(CR.sup.6R.sup.7)n- etc., each R.sup.6 and R.sup.7 are independently hydrogen, halogen etc., R.sup.2 is substituted or unsubstituted alkyl, R.sup.3 is hydrogen or substituted or unsubstituted alkyl, R.sup.4 is substituted or unsubstituted alkylcarbonyl etc.

Claims

1. A compound of Formula (I): ##STR00888## or its pharmaceutically acceptable salt, wherein R.sup.1 is substituted or unsubstituted benzoxazole, substituted or unsubstituted benzothiazole, substituted or unsubstituted phenyl, substituted or unsubstituted 1H-imidazo[4,5-c]pyridine, substituted or unsubstituted benzimidazole, substituted or unsubstituted quinazoline, substituted or unsubstituted indazole, substituted or unsubstituted 1H-imidazo[4,5-b]pyridine, substituted or unsubstituted thiazolo[4,5-c]pyridine, substituted or unsubstituted oxazolo[4,5-c]pyridine, substituted or unsubstituted 2,6-naphthyridine, or substituted or unsubstituted thiazolo[5,4-b]pyridine, ring A is substituted or unsubstituted cyclohexane, substituted or unsubstituted cyclobutane, substituted or unsubstituted tetrahydropyran, or substituted or unsubstituted 1,3-dioxane, -L.sup.1- is O(CR.sup.6R.sup.7)m-, -L.sup.2- is O(CR.sup.6R.sup.7)n-, (CR.sup.6R.sup.7)n- or C(O)(CR.sup.6R.sup.7)n-, each R.sup.6 is independently hydrogen, halogen, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl or substituted or unsubstituted alkynyl, each R.sup.7 is independently hydrogen, halogen, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl or substituted or unsubstituted alkynyl, or R.sup.6 and R.sup.7 on the same carbon atom may be taken together with the carbon atom to form a ring, or R.sup.2 is taken together with either R.sup.6 or R.sup.7 to form a ring, each m is independently an integer of 0, 1, 2 or 3, each n is independently an integer of 1, 2 or 3, R.sup.2 is substituted or unsubstituted alkyl, R.sup.3 is hydrogen or substituted or unsubstituted alkyl, and R.sup.4 is substituted or unsubstituted alkylcarbonyl, substituted or unsubstituted alkenylcarbonyl, substituted or unsubstituted alkynylcarbonyl, substituted or unsubstituted alkyloxycarbonyl, substituted or unsubstituted alkenyloxycarbonyl, substituted or unsubstituted alkynyloxycarbonyl, or substituted or unsubstituted carbamoyl.

2. The compound or its pharmaceutically acceptable salt according to claim 1, wherein ring A is substituted or unsubstituted cyclobutane, substituted or unsubstituted cyclohexane, or substituted or unsubstituted 1,3-dioxane.

3. The compound or its pharmaceutically acceptable salt according to claim 1, wherein R.sup.1 is substituted or unsubstituted benzoxazole, or substituted or unsubstituted benzothiazole.

4. The compound or its pharmaceutically acceptable salt according to claim 1, wherein R.sup.1 is substituted or unsubstituted benzothiazole, substituted or unsubstituted benzoxazole, substituted or unsubstituted benzoimidazole, substituted or unsubstituted indazole, or substituted or unsubstituted quinazoline.

5. The compound or its pharmaceutically acceptable salt according to claim 1, wherein R.sup.4 is substituted or unsubstituted alkylcarbonyl.

6. The compound or its pharmaceutically acceptable salt according to claim 5, wherein R.sup.4 is methylcarbonyl.

7. The compound or its pharmaceutically acceptable salt according to claim 1, wherein R.sup.4 is substituted or unsubstituted carbamoyl.

8. The compound or its pharmaceutically acceptable salt according to claim 1, wherein m is 0.

9. The compound or its pharmaceutically acceptable salt according to claim 1, wherein -L.sup.2- is O(CR.sup.6R.sup.7)n-.

10. The compound or its pharmaceutically acceptable salt according to claim 1, wherein n is 1.

11. The compound or its pharmaceutically acceptable salt according to claim 1, wherein -L.sup.2- is O(CR.sup.6.sup.7), and R.sup.2 is taken together with either R.sup.6 or R.sup.7 to form ring.

12. The compound or its pharmaceutically acceptable salt according to claim 1, wherein -L.sup.1- is O(CR.sup.6R.sup.7)m-, and -L.sup.2- is O(CR.sup.6R.sup.7)n- or (CR.sup.6R.sup.7)n-.

13. A pharmaceutical composition, which comprises the compound or its pharmaceutically acceptable salt according to claim 1, and a pharmaceutically acceptable additive.

14. A method for treatment of obesity and/or diabetes comprising administering an effective amount of the compound or its pharmaceutically acceptable salt according to claim 1 to a patient in need thereof.

15. The compound or its pharmaceutically acceptable salt according to claim 1, wherein ring A is substituted or unsubstituted 1,3-dioxane.

16. The compound or its pharmaceutically acceptable salt according to claim 1, wherein R.sup.1 is substituted or unsubstituted benzimidazole.

17. The compound or its pharmaceutically acceptable salt according to claim 1, wherein R.sup.1 is substituted or unsubstituted benzimidazole; ring A is substituted or unsubstituted 1,3-dioxane; and m is 0.

18. The compound or its pharmaceutically acceptable salt according to claim 1, wherein R.sup.1 is substituted benzimidazole.

19. The compound or its pharmaceutically acceptable salt according to claim 1, wherein R.sup.6 and R.sup.7 are hydrogen.

Description

MODE FOR CARRYING OUT THE INVENTION

(1) Terms used in the present description are explained below. Each term has the same meaning alone or together with other terms in this description.

(2) Halogen includes fluorine atom, chlorine atom, bromine atom, and iodine atom. Especially preferred is fluorine atom, or chlorine atom.

(3) Alkyl includes C1 to C15, preferably C1 to C10, more preferably C1 to C6, even more preferably C1 to C4 linear or branched alkyl group. Examples include methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, n-pentyl, isopentyl, neopentyl, n-hexyl, isohexyl, n-heptyl, isoheptyl, n-octyl, isooctyl, n-nonyl, n-decyl and the like.

(4) A preferable embodiment of alkyl includes methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, n-pentyl and the like. More preferably is methyl, ethyl, n-propyl, isopropyl, tert-butyl and the like.

(5) A preferable embodiment of alkyl of R.sup.2 includes methyl and the like.

(6) Alkyloxy means the above alkyl bonded to the oxygen atom. Examples are methyloxy, ethyloxy, n-propyloxy, isopropyloxy, n-butyloxy, tert-butyloxy, isobutyloxy, sec-butyloxy, pentyloxy, isopentyloxy, hexyloxy and the like. A preferable embodiment of alkyloxy includes methyloxy, ethyloxy, n-propyloxy, isopropyloxy, tert-butyloxy and the like.

(7) Alkyloxycarbonyl means a carbonyl group to which the above alkyloxy is bonded. Examples are methyloxycarbonyl, ethyloxycarbonyl, propyloxycarbonyl, isopropyloxycarbonyl, tert-butyloxycarbonyl, isobutyloxycarbonyl, sec-butyloxycarbonyl, pentyloxycarbonyl, isopentyloxycarbonyl, hexyloxycarbonyl and the like. A more preferable embodiment of alkyloxycarbonyl includes methyloxycarbonyl, ethyloxycarbonyl, propyloxycarbonyl and the like.

(8) Especially preferable embodiment of alkyloxycarbonyl of R.sup.4 includes tert-butyloxycarbonyl and the like.

(9) Alkenyl includes linear or branched alkenyl containing one or more double bond at any position having C2 to C15, preferable C2 to C10, more preferably C2 to C6, even more preferably C2 to C4. Examples include vinyl, allyl, propenyl, isopropenyl, butenyl, isobutenyl, prenyl, butadienyl, pentenyl, isopentenyl, pentadienyl, hexenyl, isohexenyl, hexadienyl, heptenyl, octenyl, nonenyl, decenyl, undecenyl, dodecenyl, toridecenyl, tetradecenyl, pentadecenyl and the like.

(10) A preferable embodiment of alkenyl includes vinyl, allyl, propenyl, isopropenyl, butenyl.

(11) Alkynyl includes linear or branched alkynyl containing one or more triple bond at any position having C2 to C15, preferably C2 to C10, more preferably C2 to C6, even more preferably C2 to C4. Examples include ethynyl, propynyl, buthynyl, pentynyl, hexynyl, heptynyl, octynyl, nonynyl, decynyl and the like. Alkynyl can have double bond(s) at any arbitrary position(s).

(12) A preferable embodiment of alkynyl includes ethynyl, propynyl, butynyl, pentynyl and the like.

(13) Alkenyloxy means the above alkenyl bonded to the oxygen atom. Examples include vinyloxy, allyloxy, 1-propenyloxy, 2-butenyloxy, 2-pentenyloxy, 2-hexenyloxy, 2-heptenyloxy, 2-octenyloxy and the like.

(14) Alkynyloxy means the above alkynyl bonded to the oxygen atom. Examples include ethynyloxy, 1-propynyloxy, 2-propynyloxy, 2-buthynyloxy, 2-pentynyloxy, 2-hexynyloxy, 2-heptynyloxy, 2-octynyloxy and the like.

(15) Alkylsulfanyl means a sulfanyl group the hydrogen atom of which is replaced by the above alkyl. Examples are methylsulfanyl, ethylsulfanyl, n-propylsulfanyl, isopropylsulfanyl, n-butylsulfanyl, tert-butylsulfanyl, isobutylsulfanyl, sec-butylsulfanyl, pentylsulfanyl, isopentylsulfanyl, hexylsulfanyl and the like. A preferable embodiment of alkylsulfanyl includes methylsulfanyl, ethylsulfanyl, n-propylsulfanyl, isopropylsulfanyl, tert-butylsulfanyl.

(16) Alkenylsulfanyl means a sulfanyl group the hydrogen atom of which is replaced by the above alkenyl. Examples include vinylsulfanyl, allylsulfanyl, 1-propenylsulfanyl, 2-butenylsulfanyl, 2-pentenylsulfanyl, 2-hexenylsulfanyl, 2-heptenylsulfanyl, 2-octenylsulfanyl and the like.

(17) Alkynylsulfanyl means a sulfanyl group the hydrogen atom of which is replaced by the above alkynyl. Examples include ethynylsulfanyl, 1-propynylsulfanyl, 2-propynylsulfanyl, 2-butynylsulfanyl, 2-pentynylsulfanyl, 2-hexynylsulfanyl, 2-heptynylsulfanyl, 2-octynylsulfanyl and the like.

(18) Alkylcarbonyl means a carbonyl group to which above alkyl is bonded. Examples include acetyl, ethylcarbonyl, propylcarbonyl, isopropylcarbonyl, tert-butylcarbonyl, isobutylcarbonyl, sec-butylcarbonyl, pentylcarbonyl, isopentylcarbonyl, hexylcarbonyl and the like. A preferable embodiment of alkylcarbonyl includes methylcarbonyl, ethylcarbonyl, n-propylcarbonyl and the like.

(19) Especially preferable embodiment of alkylcarbonyl of R.sup.4 includes methyl carbonyl and the like.

(20) Alkenylcarbonyl means a carbonyl group to which above alkenyl is bonded. Examples include ethylenylcarbonyl, propenylcarbonyl and the like.

(21) Alkynylcarbonyl means a carbonyl group to which above alkynyl is bonded. Examples include ethynylcarbonyl, propynylcarbonyl and the like.

(22) Cycloalkyl means C3 to C8 cyclic saturated hydrocarbon group and the cyclic saturated hydrocarbon group fused with one or two C3 to C8 cyclic group(s). Examples of C3 to C8 cyclic saturated carbocyclyl include cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl and the like. Especially preferable examples include C3 to C6 cycloalkyl, or C5 to C6 cycloalkyl. Furthermore, C3 cycloalkyl is preferable.

(23) The 3- to 8-membered ring fused with C3 to C8 cyclic saturated hydrocarbons group includes cycloalkane ring (e.g.: cyclohexane ring, cyclopentane ring etc.), cycloalkene ring (e.g.: cyclohexene ring, cyclopentene ring etc.), non-aromatic heterocycle (e.g.: piperidine ring, piperazine ring, morpholine ring etc.). At the above ring, the bond(s) can be attached to C3 to C8 cyclic saturated hydrocarbon group.

(24) For example, the following groups are also exemplified as a cycloalkyl, and included in cycloalkyl. These groups can be substituted at any arbitrary position(s). When cycloalkyl is substituted, the substituent(s) on the cycloalkyl can be substituted on either C3 to C8 cyclic saturated hydrocarbon group or 3- to 8-membered ring fused C3 to C8 cyclic saturated hydrocarbon group.

(25) ##STR00038##

(26) Furthermore, cycloalkyl includes a bridged group or a group formed Spiro ring as follows.

(27) ##STR00039##

(28) Cycloalkyl substituted with carboxy means the above cycloalkyl substituted with one or more carboxy.

(29) Cycloalkenyl means C3 to C8 cyclic unsaturated aliphatic hydrocarbon group and the cyclic unsaturated aliphatic hydrocarbon group fused with one or two 3- or 8-membered cycle(s). C3 to C8 cyclic unsaturated aliphatic hydrocarbon group preferably means that C3 to C8 cyclic unsaturated aliphatic hydrocarbon group has 1 to 3 double bond(s) between carbon atom and carbon atom in the ring. Specifically, preferred is cyclopropenyl, cyclobutenyl, cyclopentenyl, cyclohexenyl, cycloheptenyl, cyclohexadienyl and the like. Especially preferred is C3 to C6 cycloalkenyl or C5 or C6 cycloalkenyl.

(30) The ring fused with C3 to C8 cyclic unsaturated aliphatic hydrocarbon group includes carbocycle (aromatic carbocycle (e.g.: benzene ring, naphthalene ring etc.), cycloalkane ring (e.g.: cyclohexane ring, cyclopentane ring etc.), cycloalkene ring (e.g.: cyclohexene ring, cyclopentene ring etc.) and the like), heterocycle (aromatic heterocycle (pyridine ring, pyrimidine ring, pyrrole ring, imidazole ring etc.), non-aromatic heterocycle (e.g.: piperidine ring, piperazine ring, morpholine ring etc.)).

(31) At the above ring, the bond(s) can be attached to C3 to C8 cyclic unsaturated aliphatic hydrocarbon group.

(32) For example, the following groups are also exemplified as a cycloalkenyl and include in cycloalkenyl. These groups can be substituted at any arbitrary position(s). When cycloalkenyl is substituted, the substituent(s) on the cycloalkenyl can be substituted on either C3 to C8 cyclic unsaturated aliphatic hydrocarbon group or 3- to 8-membered ring fused C3 to C8 cyclic unsaturated aliphatic hydrocarbon group.

(33) ##STR00040##

(34) In addition, the cycloalkenyl also includes a group to form a spiro ring as follows:

(35) ##STR00041##

(36) Non-aromatic carbocyclyl includes above cycloalkyl and cycloalkenyl.

(37) Aromatic carbocyclyl means monocyclic or polycyclic aromatic carbocyclyl and the monocyclic or polycyclic aromatic carbocyclyl fused with one or two 3- to 8-membered ring. Examples of monocyclic or polycyclic aromatic carbocyclyl include phenyl, naphthyl, anthryl, phenanthryl. Especially phenyl is preferred.

(38) The ring fused with monocyclic or polycyclic includes non-aromatic carbocycle (e.g.: cycloalkane ring (e.g.: cyclohexane ring, cyclopentane ring etc.), cycloalkene ring (e.g.: cyclohexene ring, cyclopentene ring etc.) and the like), non-aromatic heterocycle (e.g.: piperidine ring, piperazine ring, morpholine ring etc.).

(39) At the above ring, the bond(s) can be attached to monocyclic or polycyclic aromatic carbocycle.

(40) For example, the following groups are also exemplified as an aromatic carbocyclyl and included in aromatic carbocyclyl. These groups can be substituted at any arbitrary position(s). When aromatic carbocyclyl is substituted, the substituent(s) on the aromatic carbocyclyl group can be substituted on either monocyclic or polycyclic aromatic carbocyclyl or 3- to 8-membered ring fused monocyclic or polycyclic aromatic carbocyclyl group.

(41) ##STR00042##

(42) Fused aromatic carbocyclyl means polycyclic aromatic carbocyclyl, monocyclic or polycyclic aromatic carbocyclyl fused with one or two 3- to 8-membered ring. Examples of monocyclic or polycyclic aromatic carbocyclyl include phenyl, naphthyl, anthryl, phenanthryl. Especially, preferable example is phenyl.

(43) The ring fused with monocyclic or polycyclic includes non-aromatic carbocycle (e.g.: cycloalkane ring (e.g.: cyclohexane ring, cyclopentane ring etc.), cycloalkene ring (e.g.: cyclohexene ring, cyclopentene ring etc.) and the like), non-aromatic heterocycle (e.g.: piperidine ring, piperazine ring, morpholine ring etc.).

(44) At the above ring, the bond(s) can be attached to monocyclic or polycyclic aromatic carbocycle.

(45) For example, the following groups are also exemplified as an aromatic carbocyclyl and included in aromatic carbocyclyl. These groups can be substituted at any arbitrary position(s). When aromatic carbocyclyl is substituted, the substituent(s) on the aromatic carbocyclyl group can be substituted on either monocyclic or polycyclic aromatic carbocyclyl or 3- to 8-membered ring fused monocyclic or polycyclic aromatic carbocyclyl group.

(46) For example, the following groups are exemplified as an aromatic carbocyclyl or fused aromatic carbocyclyl, and included in aromatic carbocyclyl or fused aromatic carbocyclyl. These groups are optionally substituted at any arbitrary replaceable position. When aromatic carbocyclyl or fused aromatic carbocyclyl is substituted, the substituent(s) on the aromatic carbocyclyl or the fused aromatic carbocyclyl may be substituted on either monocyclic or fused aromatic carbocyclyl or 3- to 8-membered ring fused monocyclic or fused aromatic carbocyclyl.

(47) ##STR00043##

(48) Substituted aromatic carbocyclyl includes an aromatic carbocyclyl substituted with oxo. Substituted fused aromatic carbocyclyl include a fused aromatic carbocyclyl substituted with oxo. Aromatic carbocyclyl substituted with oxo and fused aromatic carbocyclyl substituted with oxo means that two hydrogen atom on 3- to 8-membered ring fused monocyclic or polycyclic aromatic carbocyclyl constituting aromatic carbocyclyl are substituted with O group. As a aromatic carbocyclyl substituted with oxo and fused aromatic carbocyclyl substituted with oxo, the following formula:

(49) ##STR00044##
are exemplified.

(50) Aromatic heterocyclyl means monocyclic or polycyclic aromatic heterocyclyl containing one or more heteroatom(s) arbitrarily selected from O, S and N on the ring or the monocyclic or polycyclic aromatic heterocyclyl with one or two 3- to 8-membered ring, and includes monocyclic aromatic heterocyclyl and fused aromatic heterocyclyl.

(51) Especially preferable examples of monocyclic aromatic heterocyclyl are 5- or 6-membered aromatic heterocyclyl. For example, pyrrolyl, imidazolyl, pyrazolyl, pyridyl, pyridadinyl, pyrimidinyl, pyrazinyl, triazoryl, triazinyl, tetrazolyl, isooxazolyl, oxazolyl, oxadiazolyl, isothiazolyl, thiazolyl, thiadiazolyl, furyl, thienyl and the like are exemplified.

(52) Especially preferable examples of fused aromatic heterocyclyl are aromatic heterocyclyl fused with 5- or 6-membered ring. Examples include bicyclic aromatic heterocyclyl: e.g., indolyl, isoindolyl, indazolyl, indolizinyl, quinolinyl, isoquinolinyl, cinnolinyl, phthalazinyl, quinazolinyl, naphthylidinyl, quinoxalinyl, purinyl, pteridinyl, benzimidazolyl, benzisooxazolyl, benzoxazolyl, benzoxadiazoryl, benzisothiazolyl, benzothiazolyl, benzothiadiazolyl, benzofuryl, isobenzofuryl, benzothienyl, benzotriazoryl, imidazopyridyl, triazolopyridyl, imidazothiazolyl, pyrazinopyridazinyl, oxazolopyridyl, thiazolopyridyl; and tricyclic aromatic heterocyclyl: carbazolyl, acridinyl, xanthenyl, phenothiadinyl, phenoxathiinyl, phenoxadinyl, dibenzofuryl. When aromatic heterocyclyl is fused aromatic heterocyclyl, the bond(s) may be attached to any ring.

(53) As a ring fused with monocyclic or fused aromatic heterocyclyl, for example, cycloalkane ring (e.g.: cyclohexane ring, cyclopentane ring etc.), cycloalkene ring (e.g.: cyclohexene ring, cyclopentene ring etc.), non-aromatic heterocycle (e.g.: piperidine ring, piperazine ring, morpholine ring etc.) and the like are exemplified. The bond(s) can be attached to monocyclic or fused aromatic heterocyclyl containing one or more heteroatom(s) arbitrarily selected from O, S and N on the ring.

(54) For example, the following groups include also aromatic heterocyclyl. These groups can be substituted at any arbitrary replaceable position(s). When aromatic heterocyclyl is substituted, the substituent(s) on the aromatic heterocyclyl may be substituted on either monocyclic or fused aromatic heterocyclyl or 3- to 8-membered ring fused with monocyclic or fused aromatic heterocyclyl group.

(55) ##STR00045##

(56) Substituted aromatic heterocyclyl includes aromatic heterocyclyl substituted with oxo. Aromatic heterocyclyl substituted with oxo means that two hydrogen atoms bonded to the carbon atom on 3- to 8-membered ring fused monocyclic or polycyclic aromatic heterocycle constituting aromatic heterocyclyl are substituted with O group. As a aromatic heterocyclyl substituted with oxo and fused aromatic heterocyclyl substituted with oxo, the following formula:

(57) ##STR00046##
are exemplified.

(58) Especially preferable embodiments of fused aromatic carbocycly of R.sup.1 include tetrabenzooxazepinyl, tetrahydroisoquinolinyl, benzothiazolyl, dihydrobenzothiazolyl, dihydrobenzoisoxazolyl and the like.

(59) Non-aromatic heterocyclyl means a monocyclic non-aromatic heterocyclyl containing one or more heteroatom(s) arbitrarily selected from O, S and N on the ring and the monocyclic non-aromatic heterocyclyl fused with one or two 3- to 8-membered cyclic group(s) (polycyclic non-aromatic heterocyclyl group(s).

(60) Preferable examples of monocyclic non-aromatic heterocyclyl are a monocyclic non-aromatic heterocyclyl group containing 1 to 4 heteroatom(s) arbitrarily selected from O, S and N on the ring. Specifically, dioxanyl, thiiranyl, oxiranyl, oxathiolanyl, azetidinyl, thianyl, pyrrolidinyl, pyrrolinyl, imidazolidinyl, imidazolinyl, pyrazolidinyl, pyrazolinyl, piperidyl, piperidino, piperazinyl, piperadino, morpholinyl, morpholino, oxadiazinyl, dihydropyridyl, thiomorpholinyl, thiomorpholino, tetrahydrofuryl, tetrahydropyranyl, tetrahydrothiazolyl, tetrahydroisothiazolyl, oxazolidyl, thiazolidyl, oxetanyl, thiazolidinyl, tetrahydropyridyl, dihydrothiazolyl, dihydrooxazinyl, hexahydroazepinyl, tetrahydrodiazepinyl, tetrahydropyridazinyl, hexahydropyrimidinyl, dioxolanyl, dioxazinyl, aziridinyl, dioxolinyl, oxepanyl, thiolanyl, thiazinyl, thiazinyl and the like are exemplified.

(61) As a ring fused with monocyclic non-aromatic heterocyclyl containing one or more heteroatom(s) arbitrarily selected from O, S and N on the ring, for example, carbocycle (aromatic hydrocarbon ring (e.g.: benzene ring, naphthalene ring etc.), cycloalkane ring (e.g.: cyclohexane ring, cyclopentane ring etc.), cycloalkene ring (e.g.: cyclohexene ring, cyclopenten ring etc.) and the like), heterocycle (aromatic heterocycle (pyridine ring, pyrimidine ring, pyrrole ring, imidazole ring etc), non-aromatic heterocycle (e.g.: piperidine ring, piperazine ring, morpholine ring etc.).

(62) As a polycyclic non-aromatic heterocyclyl, for example, indolinyl, isoindolinyl, chromanyl, isochromanyl and the like are exemplified.

(63) When non-aromatic heterocyclyl is polycyclic non-aromatic heterocyclyl, the bond(s) can be attached to non-aromatic heterocyclyl containing one or more heteroatom(s) arbitrarily selected from O, S and N on the ring. For example, the following groups include also non-aromatic heterocyclyl. These groups can be substituted at any arbitrary position(s). When non-aromatic heterocyclyl is substituted, the substituent(s) on the non-aromatic heterocyclyl can be substituted on either monocyclic or polycyclic non-aromatic heterocyclyl or 3- to 8-membered fused monocyclic or polycyclic non-aromatic heterocyclyl group.

(64) ##STR00047## ##STR00048##

(65) Non-aromatic heterocyclyl include a ring having a bridge or a ring to form a spiro ring.

(66) ##STR00049##

(67) Regarding the above cycloalkyl, cycloalkenyl, non-aromatic carbocyclyl, aromatic carbocyclyl, aromatic heterocyclyl and non-aromatic heterocyclyl, non-aromatic carbocycle, non-aromatic carbocycle, non-aromatic heterocycle, aromatic carbocycle, aromatic heterocycle, carbocycle and heterocycle which is defined as fused ring mean as follows. When the ring is substituted, the ring may have the substitutent on the fused ring. Non-aromatic carbocycle and non-aromatic heterocycle may be substituted with oxo.

(68) Non-aromatic carbocycle means C3 to C8 cyclic saturated hydrocarbon ring and C3 to C8 cyclic unsaturated aliphatic hydrocarbon ring. For example, cyclohexane ring, cyclopentane ring, cyclohexene ring, cyclopentene ring and the like are exemplified.

(69) Non-aromatic heterocycle means 3- to 8-membered non-aromatic heterocycle containing one to four heteroatom(s) arbitrarily selected from O, S and N on the ring. For example, piperidine ring, piperazine ring, morpholine ring and the like are exemplified.

(70) Aromatic carbocycle means monocyclic or polycyclic aromatic carbocycle. For example, benzene ring, naphthalene ring and the like are exemplified.

(71) Aromatic heterocycle means monocyclic or polycyclic aromatic heterocycle containing one or more heteroatom(s) arbitrarily selected from O, S and N on the ring. For example, pyridine ring, pyrimidine ring, pyrrole ring, imidazole ring and the like are exemplified.

(72) Carbocycle includes the above non-aromatic carbocycle and aromatic carbocycle.

(73) Heterocycle includes the above non-aromatic heterocycle and aromatic heterocycle.

(74) Non-aromatic carbocyclyloxy means the above non-aromatic carbocyclyl bonded to an oxygen atom. For example, cyclopropyloxy, cyclohexyloxy, cyclohexenyloxy, cyclopropenyloxy, cyclobutenyloxy, cyclopentenyloxy, cyclohexenyloxy, cycloheptenyloxy, cyclohexadienyloxy and the like are exemplified.

(75) Aromatic carbocyclyloxy means the above aromatic carbocyclyl bonded to an oxygen atom. For example, phenyloxy, naphthyloxy and the like are exemplified.

(76) Aromatic heterocyclyloxy means the above aromatic heterocyclyl bonded to an oxygen atom. For example, pyridyloxy, oxazolyloxy and the like are exemplified.

(77) Non-aromatic heterocyclyloxy means the above non-aromatic heterocyclyl bonded to an oxygen atom. For example, piperidinyloxy, tetrahydro furyloxy and the like are exemplified.

(78) Non-aromatic carbocyclylcarbonyl means the above cycloalkyl or cycloalkenyl bonded to a carbonyl group. For example, cyclopropylcarbonyl, cyclohexylcarbonyl, cyclohexenylcarbonyl, cyclohexenylcarbonyl and the like are exemplified.

(79) Aromatic carbocyclylcarbonyl means the above aromatic carbocyclyl bonded to a carbonyl group. For example, phenylcarbonyl, naphthylcarbonyl and the like are exemplified.

(80) Aromatic heterocyclylcarbonyl means the above aromatic heterocyclyl bonded to a carbonyl group. For example, pyridylcarbonyl, oxazolylcarbonyl, isoxazolylcarbonyl, pyrazolylcarbonyl, thiazolylcarbonyl, isothiazolylcarbonyl, thienylcarbonyl, pyrrolylcarbonyl, furylcarbonyl and the like are exemplified.

(81) Examples of aromatic heterocyclylcarbonyl of R.sup.4 include pyrrolylcarbonyl and the like.

(82) Non-aromatic heterocyclylcarbonyl means the above non-aromatic heterocyclyl bonded to a carbonyl group. For example, oxetanylcarbonyl, piperidinylcarbonyl, tetrahydrofurylcarbonyl and the like are exemplified.

(83) Examples of non-aromatic heterocyclylcarbonyl of R.sup.4 include oxetanylcarbonyl and the like.

(84) Alkylsulfonyl means the above alkyl bonded to a sulfonyl group. For example, methylsulfonyl, ethylsulfonyl, propylsulfonyl, isopropylsulfonyl, tert-butylsulfonyl, isobutylsulfonyl, sec-butylsulfonyl and the like are exemplified.

(85) A preferable embodiment of alkylsulfonyl includes methylsulfonyl, ethylsulfonyl.

(86) Examples of alkylsulfonyl of R.sup.4 include methylsulfonyl, ethylsulfonyl and the like.

(87) Alkenylsulfonyl means the above alkenyl bonded to a sulfonyl group. For example, ethylenylsulfonyl, propenylsulfonyl and the like are exemplified.

(88) Alkynylsulfonyl means the above alkynyl bonded to a sulfonyl group. For example, ethynylsulfonyl, propynylsulfonyl and the like are exemplified.

(89) Non-aromatic carbocyclylsulfonyl means the above non-aromatic carbocyclyl bonded to a sulfonyl group. For example, cyclopropylsulfonyl, cyclopentanylsulfonyl, cyclohexylsulfonyl, cyclopropenylsulfonyl, cyclopentenylsulfonyl, cyclohexenylsulfonyl and the like are exemplified.

(90) Aromatic carbocyclylsulfonyl means the above aromatic carbocyclyl bonded to a sulfonyl group. For example, phenylsulfonyl, naphthylsulfonyl and the like are exemplified.

(91) Aromatic heterocyclylsulfonyl means the above aromatic heterocyclyl bonded to a sulfonyl group. For example, pyridylsulfonyl, oxazolylsulfonyl and the like are exemplified.

(92) Non-aromatic heterocyclylsulfonyl means the above non-aromatic heterocyclyl bonded to a sulfonyl group. For example, piperidinylsulfonyl, tetrahydrofurylsulfonyl and the like are exemplified.

(93) Alkenyloxycarbonyl means the above alkenyloxy bonded to a carbonyl group. For example, ethylenyloxycarbonyl, propenyloxycarbonyl and the like are exemplified.

(94) Alkynyloxycarbonyl means the above alkynyloxy bonded to a carbonyl group. For example, ethynyloxycarbonyl, propynyloxycarbonyl and the like are exemplified.

(95) Aromatic carbocyclyloxycarbonyl means the above aromatic carbocyclyloxy bonded to a carbonyl group. For example, phenyloxycarbonyl, naphthyloxycarbonyl and the like are exemplified.

(96) Non-aromatic carbocyclyloxycarbonyl means the above non-aromatic carbocyclyloxy bonded to a carbonyl group. For example, cyclopropyloxycarbonyl, cyclohexyloxycarbonyl, cyclohexenyloxycarbonyl, cyclopropenyloxycarbonyl and the like are exemplified.

(97) Aromatic heterocyclyloxycarbonyl means the above aromatic heterocyclyloxy bonded to a carbonyl group. For example, pyridyloxycarbonyl, oxazolyloxycarbonyl and the like are exemplified.

(98) Non-aromatic heterocyclyloxycarbonyl means the above non-aromatic heterocyclyloxy bonded to a carbonyl group. For example, piperidinyloxycarbonyl, tetrahydrofuryloxycarbonyl and the like are exemplified.

(99) Non-aromatic carbocyclylsulfanyl means a sulfanyl group the hydrogen atom of which is replaced by the above non-aromatic carbocyclyl. For example, cyclopropylsulfanyl, cyclohexylsulfanyl, cyclohexenylsulfanyl, cyclopropenylsulfanyl, cyclobutenylsulfanyl, cyclohexenylsulfanyl, cyclopentenylsulfanyl, cycloheptenylsulfanyl, cyclohexadienylsulfanyl and the like are exemplified.

(100) Aromatic carbocyclylsulfanyl means a sulfanyl group the hydrogen atom of which is replace by the above aromatic carbocyclyl. For example, phenylsulfanyl, naphthylsulfanyl and the like are exemplified.

(101) Aromatic heterocyclylsulfanyl means a sulfanyl group the hydrogen atom of which is replaced by the above aromatic heterocyclyl. For example, pyridylsulfanyl, oxazolylsulfanyl and the like are exemplified.

(102) Non-aromatic heterocyclylsulfanyl means a sulfanyl group the hydrogen atom of which is replaced by the above non-aromatic heterocyclyl. For example, piperidinylsulfanyl, tetrahydrofurylsulfanyl and the like are exemplified.

(103) Alkylsulfinyl means the above alkyl bonded to a sulfinyl group. For example, methylsulfinyl, ethylsulfinyl, n-propylsulfinyl, isopropylsulfinyl and the like are exemplified.

(104) Alkenylsulfinyl means the above alkenyl bonded to a sulfinyl group. For example, ethylenylsulfinyl, propenylsulfinyl and the like are exemplified.

(105) Alkynylsulfinyl means the above alkynyl bonded to a sulfinyl group. For example, ethynylsulfinyl, propynylsulfinyl and the like are exemplified.

(106) Non-aromatic carbocyclylsulfinyl means the above non-aromatic carbocyclyl bonded to a sulfinyl group. For example, cyclopropylsulfinyl, cyclohexylsulfinyl, cyclohexenylsulfinyl, cyclopropenylsulfinyl, cyclobutenylsulfinyl, cyclohexenylsulfinyl, cyclopentenylsulfinyl, cycloheptenylsulfinyl, cyclohexadienylsulfinyl and the like are exemplified.

(107) Aromatic carbocyclylsulfinyl means the above aromatic carbocyclyl bonded to a sulfinyl group. For example, phenylsulfinyl, naphthylsulfinyl and the like are exemplified.

(108) Aromatic heterocyclyl sulfinyl means the above aromatic heterocyclyl bonded to a sulfinyl group. For example, pyridylsulfinyl, oxazolylsulfinyl and the like are exemplified.

(109) Non-aromatic heterocyclyl sulfinyl means the above non-aromatic heterocyclyl bonded to a sulfinyl group. For example, piperidinylsulfinyl, tetrahydrofurylsulfinyl and the like are exemplified.

(110) Aminosulfinyl means an amino group bonded to a sulfinyl group.

(111) Alkylsulfonyloxy means the above alkylsulfonyl bonded to an oxygen atom. For example, methylsulfonyloxy, ethylsulfonyloxy, propylsulfonyloxy, isopropylsulfonyloxy, tert-butylsulfonyloxy, isobutylsulfonyloxy, sec-butylsulfonyloxy and the like are exemplified.

(112) A preferable embodiment of alkylsulfonyloxy includes methylsulfonyloxy, ethylsulfonyloxy and the like.

(113) Alkenylsulfonyloxy means the above alkenylsulfonyl bonded to an oxygen atom. For example, ethylenylsulfonyloxy, propenylsulfonyloxy and the like are exemplified.

(114) Alkynylsulfonyloxy means the above alkynylsulfonyl bonded to an oxygen atom. For example, ethynylsulfonyloxy, propynylsulfonyloxy and the like are exemplified.

(115) Non-aromatic carbocyclylsulfonyloxy means the above non-aromatic carbocyclylsulfonyl bonded to an oxygen atom. For example, cyclopropylsulfonyloxy, cyclohexylsulfonyloxy, cyclohexenylsulfonyloxy, cyclopropenylsulfonyloxy, cyclohexenylsulfonyloxy and the like are exemplified.

(116) Aromatic carbocyclylsulfonyloxy means the above aromatic carbocyclylsulfonyl bonded to an oxygen atom. For example, phenylsulfonyloxy, naphthylsulfonyloxy and the like are exemplified.

(117) Aromatic heterocyclylsulfonyloxy means the above aromatic heterocyclylsulfonyl bonded to an oxygen atom. For example, pyridylsulfonyloxy, oxazolylsulfonyloxy and the like are exemplified.

(118) Non-aromatic heterocyclylsulfonyloxy means the above non-aromatic heterocyclylsulfonyl bonded to an oxygen atom. For example, piperidinylsulfonyloxy, tetrahydrofurylsulfonyloxy and the like are exemplified.

(119) Alkylcarbonyloxy means the above alkylcarbonyl bonded to an oxygen atom. Examples of alkylcarbonyloxy include methylcarbonyloxy, ethylcarbonyloxy, propylcarbonyloxy, isopropylcarbonyloxy, tert-butylcarbonyloxy, isobutylcarbonyloxy, sec-butylcarbonyloxy and the like.

(120) A preferable embodiment of alkylcarbonyloxy includes methylcarbonyloxy, ethylcarbonyloxy and the like.

(121) Alkenylcarbonyloxy means the above alkenylcarbonyl bonded to an oxygen atom. For example, ethylenylcarbonyloxy, propenylcarbonyloxy and the like are exemplified.

(122) Alkynylcarbonyloxy means the above alkynylcarbonyl bonded to an oxygen atom. For example, ethynylcarbonyloxy, propynylcarbonyloxy and the like are exemplified.

(123) Non-aromatic carbocyclylcarbonyloxy means the above non-aromatic carbocyclylcarbonyl bonded to an oxygen atom. Examples of cycloalkylcarbonyloxy include cyclopropylcarbonyloxy, cyclohexylcarbonyloxy, cyclohexenylcarbonyloxy and the like.

(124) Aromatic carbocyclylcarbonyloxy means the above aromatic carbocyclylcarbonyl bonded to an oxygen atom. Examples of aromatic carbocyclylcarbonyloxy include phenylcarbonyloxy, naphthylcarbonyloxy and the like.

(125) Aromatic heterocyclylcarbonyloxy means the above aromatic heterocyclylcarbonyl bonded to an oxygen atom. Example of aromatic heterocyclylcarbonyloxy include pyridylcarbonyloxy, oxazolylcarbonyloxy and the like are exemplified.

(126) Non-aromatic heterocyclylcarbonyloxy means the above non-aromatic heterocyclylcarbonyl bonded to an oxygen atom. Examples of non-aromatic heterocyclylcarbonyloxy include piperidinylcarbonyloxy, tetrahydrofurylcarbonyloxy and the like are exemplified.

(127) Alkyloxycarbonyl means the above alkyloxy bonded to a carbonyl group. Examples of alkyloxycarbonyl include methyloxycarbonyl, ethyloxycarbonyl, propyloxycarbonyl, isopropyloxycarbonyl, tert-butyloxycarbonyl, isobutyloxycarbonyl, sec-butyloxycarbonyl, pentyloxycarbonyl, isopentyloxycarbonyl, hexyloxycarbonyl and the like are exemplified. A preferable embodiment of alkyloxycarbonyl includes methyloxycarbonyl, ethyloxycarbonyl, propyloxycarbonyl and the like.

(128) A preferable embodiment of alkyloxycarbonyl of R.sup.4 includes methyloxycarbonyl, ethyloxycarbonyl.

(129) Alkenyloxycarbonyl means the above alkenyloxy bonded to a carbonyl group. Examples of alkenyloxycarbonyl include ethylenyloxycarbonyl, propenyloxycarbonyl and the like.

(130) Alkynyloxycarbonyl means the above alkynyloxy bonded to a carbonyl group. Examples of alkynyloxycarbonyl include ethynyloxycarbonyl, propynyloxycarbonyl and the like.

(131) Non-aromatic carbocyclyloxycarbonyl means the above non-aromatic carbocyclyloxy bonded to a carbonyl group. For example, cyclopropyloxycarbonyl, cyclopentynyloxycarbonyl, cyclohexyloxycarbonyl, cyclopropenyloxycarbonyl, cyclopentenyloxycarbonyl, cyclohexenyloxycarbonyl and the like are exemplified.

(132) Aromatic carbocyclyloxycarbonyl means the above aromatic carbocyclyloxy bonded to a carbonyl group. For example, phenyloxycarbonyl, naphthyloxycarbonyl and the like are exemplified.

(133) Aromatic heterocyclyloxycarbonyl means the above aromatic heterocyclyloxy bonded to a carbonyl group. For example, pyridyloxycarbonyl, oxazolyloxycarbonyl and the like are exemplified.

(134) Non-aromatic heterocyclyloxycarbonyl means the above non-aromatic heterocyclyloxy bonded to a carbonyl group. For example, piperidinyloxycarbonyl, tetrahydrofuryloxycarbonyl and the like are exemplified.

(135) Substituents on the nitrogen atom insubstituted or unsubstituted amino, substituted or unsubstituted carbamoyl, substituted or unsubstituted sulfamoyl, substituted or unsubstituted amidino and substituted or unsubstituted amino sulfinyl include the following substituents. Hydrogen on the nitrogen atom can be replaced with one or two substituents selected from the following substituents.

(136) Substituents:

(137) alkyl, alkenyl, alkynyl, haloalkyl, haloalkenyl, halogen, hydroxy, carboxy, formyl, formyloxy, carbamoyl, sulfamoyl, sulfanyl, sulfino, sulfo, thioformyl, thiocarboxy, dithiocarboxy, thiocarbamoyl, cyano, nitro, nitroso, azido, hydradino, ureido, amidino, guanidino, trialkylsilyl, alkyloxy, alkyloxyalkyloxy, alkenyloxy, alkynyloxy, haloalkyloxy, trialkylsilyloxy, cyanoalkyloxy, alkylcarbonyl, haloalkylcarbonyl, carbamoylalkylcarbonyl, alkenylcarbonyl, alkynylcarbonyl, monoalkylamino, dialkylamino, alkylsulfonyl, alkenylsulfonyl, alkynylsulfonyl, monoalkylcarbonylamino, dialkylcarbonylamino, monoalkylsulfonylamino, dialkylsulfonylamino, alkylimino, alkenylimino, alkynylimino, alkylcarbonylimino, alkenylcarbonylimino, alkynylcarbonylimino, alkyloxyimino, alkenyloxyimino, alkynyloxyimino, alkylcarbonyloxy, alkenylcarbonyloxy, alkynylcarbonyloxy, alkyloxycarbonyl, monoalkyloxycarbonylamino, dialkyloxycarbonylamino, alkenyloxycarbonyl, alkynyloxycarbonyl, alkylsulfanyl, alkylcarbonylsulfanyl, alkenylsulfanyl, alkynylsulfanyl, alkylsulfinyl, alkenylsulfinyl, alkynylsulfinyl, monoalkylcarbamoyl, mono(hydroxyalkyl)carbamoyl, dialkylcarbamoyl, hydroxycarbamoyl, cyanocarbamoyl, carboxyalkylcarbamoyl, mono(dialkylaminoalkyl)carbamoyl di(dialkylaminoalkyl)carbamoyl, non-aromatic carbocyclylalkylcarbamoyl, non-aromatic carbocyclylcarbamoyl, non-aromatic heterocyclylalkylcarbamoyl, non-aromatic heterocyclylcarbamoyl, monoalkyloxycarbamoyl, dialkyloxycarbamoyl, monoalkyloxycarbonylalkylcarbamoyl, dialkyloxycarbonylalkylcarbamoyl, monoalkylsulfamoyl, dialkylsulfamoyl, aromatic carbocyclyl, non-aromatic carbocyclyl, aromatic heterocyclyl, non-aromatic heterocyclyl, aromatic carbocyclyloxy, non-aromatic carbocyclyloxy, non-aromatic heterocyclyloxy, non-aromatic heterocyclyloxy, aromatic carbocyclylcarbonyl, non-aromatic carbocyclylcarbonyl, aromatic heterocyclylcarbonyl, non-aromatic heterocyclylcarbonyl, non-aromatic carbocyclylcarbonyloxy, aromatic carbocyclylcarbonyloxy, aromatic heterocyclylcarbonyloxy, non-aromatic heterocyclylcarbonyloxy, aromatic carbocyclyloxycarbonyl, non-aromatic carbocyclyloxycarbonyl, aromatic heterocyclyloxycarbonyl, non-aromatic heterocyclyloxycarbonyl, aromatic carbocyclylalkyl, non-aromatic carbocyclylalkyl, aromatic heterocyclylalkyl, non-aromatic heterocyclylalkyl, aromatic carbocyclylalkyloxy, non-aromatic carbocyclylalkyloxy, aromatic heterocyclylalkyloxy, non-aromatic heterocyclylalkyloxy, aromatic carbocyclylalkyloxycarbonyl, non-aromatic carbocyclylalkyloxycarbonyl, aromatic heterocyclylalkyloxycarbonyl, non-aromatic heterocyclylalkyloxycarbonyl, aromatic carbocyclylalkylamino, non-aromatic carbocyclylalkylamino, aromatic heterocyclylalkylamino, non-aromatic heterocyclylalkylamino, aromatic carbocyclylsulfanyl, non-aromatic carbocyclylsulfanyl, aromatic heterocyclylsulfanyl, non-aromatic heterocyclylsulfanyl, aromatic carbocyclylsulfonyl, non-aromatic carbocyclylsulfonyl, aromatic heterocyclylsulfonyl, non-aromatic heterocyclylsulfonyl, alkylsulfonyloxy, alkenylsulfonyloxy, alkynylsulfonyloxy, non-aromatic carbocyclylsulfonyloxy, aromatic carbocyclylsulfonyloxy, aromatic heterocyclylsulfonyloxy, non-aromatic heterocyclylsulfonyloxy, alkyloxycarbonylalkyl, carboxyalkyl, hydroxyalkyl, dialkylaminoalkyl, hydroxyalkyl, alkyloxyalkyl, aromatic carbocyclylalkyloxyalkyl, non-aromatic carbocyclylalkyloxyalkyl, aromatic heterocyclylalkyloxyalkyl and non-aromatic heterocyclylalkyloxyalkyl.

(138) Substituents of the above substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkyloxy,

(139) substituted or unsubstituted alkenyloxy, substituted or unsubstituted alkynyloxy, substituted or unsubstituted alkyl sulfanyl, substituted or unsubstituted alkenylsulfanyl, substituted or unsubstituted alkynylsulfanyl, substituted or unsubstituted alkylcarbonyl, substituted or unsubstituted alkenylcarbonyl, substituted or unsubstituted alkynylcarbonyl, substituted or unsubstituted alkylsulfonyl, substituted or unsubstituted alkenylsulfonyl, substituted or unsubstituted alkynylsulfonyl, substituted or unsubstituted alkyloxycarbonyl, substituted or unsubstituted alkenyloxycarbonyl, substituted or unsubstituted alkynyloxycarbonyl, substituted or unsubstituted alkylsulfinyl, substituted or unsubstituted alkenylsulfinyl, substituted or unsubstituted alkynylsulfinyl, substituted or unsubstituted alkyl sulfonyloxy, substituted or unsubstituted alkenylsulfonyloxy, substituted or unsubstituted alkynylsulfonyloxy, substituted or unsubstituted alkylcarbonyloxy, substituted or unsubstituted alkenylcarbonyloxy and substituted or unsubstituted alkynylcarbonyloxy include the following substituents. Hydrogen atom on the carbon atom at arbitrary position(s) can be replaced with one or more substituents selected from the following substituents.
Substituents:
halogen, hydroxy, carboxy, amino, imino, hydroxyamino, hydroxyimino, formyl, formyloxy, carbamoyl, sulfamoyl, sulfanyl, sulfino, sulfo, thioformyl, thiocarboxy, dithiocarboxy, thiocarbamoyl, cyano, nitro, nitroso, azido, hydradino, ureido, amidino, guadinino, trialkylsilyl, alkyloxy, alkyloxyalkyloxy, alkenyloxy, alkynyloxy, haloalkyloxy, trialkylsilyloxy, cyanoalkyloxy, alkylcarbonyl, haloalkylcarbonyl, carbamoylalkylcarbonyl, alkenylcarbonyl, alkynylcarbonyl, monoalkylamino, dialkylamino, alkylsulfonyl, alkenylsulfonyl, alkynylsulfonyl, monoalkylcarbonylamino, dialkylcarbonylamino, monoalkylsulfonylamino, dialkylsulfonylamino, alkylimino, alkenylimino, alkynylimino, alkylcarbonylimino, alkenylcarbonylimino, alkynylcarbonylimino, alkyloxyimino, alkenyloxyimino, alkynyloxyimino, alkylcarbonyloxy, alkenylcarbonyloxy, alkynylcarbonyloxy, alkyloxycarbonyl, monoalkyloxycarbonylamino, dialkyloxycarbonylamino, alkenyloxycarbonyl, alkynyloxycarbonyl, alkylsulfanyl, alkylcarbonylsulfanyl, alkenylsulfanyl, alkynylsulfanyl, alkylsulfinyl, alkenylsulfinyl, alkynylsulfinyl, monoalkylcarbamoyl, mono(hydroxyalkyl)carbamoyl, dialkylcarbamoyl, hydroxycarbamoyl, cyanocarbamoyl, carboxyalkylcarbamoyl, mono(dialkylaminoalkyl)carbamoyl di(dialkylaminoalkyl)carbamoyl, non-aromatic carbocyclylcarbamoyl, non-aromatic heterocyclylalkylcarbamoyl, non-aromatic heterocyclylcarbamoyl, monoalkyloxycarbamoyl, dialkyloxycarbamoyl, monoalkyloxycarbonylalkylcarbamoyl, dialkyloxycarbonylalkylcarbamoyl, monoalkylsulfamoyl, dialkylsulfamoyl, aromatic carbocyclyl, non-aromatic carbocyclyl, aromatic heterocyclyl, non-aromatic heterocyclyl, aromatic carbocyclyloxy, non-aromatic carbocyclyloxy, aromatic heterocyclyloxy, non-aromatic heterocyclyloxy, aromatic carbocyclylcarbonyl, non-aromatic carbocyclylcarbonyl, aromatic heterocyclylcarbonyl, non-aromatic heterocyclylcarbonyl, non-aromatic carbocyclylcarbonyloxy, aromatic carbocyclylcarbonyloxy, aromatic heterocyclylcarbonyloxy, non-aromatic heterocyclylcarbonyloxy, aromatic carbocyclyloxycarbonyl, non-aromatic carbocyclyloxycarbonyl, aromatic heterocyclyloxycarbonyl, non-aromatic heterocyclyloxycarbonyl, aromatic carbocyclylalkyloxy, non-aromatic carbocyclylalkyloxy, aromatic heterocyclylalkyloxy, non-aromatic heterocyclylalkyloxy, aromatic carbocyclylalkyloxycarbonyl, non-aromatic carbocyclylalkyloxycarbonyl, aromatic heterocyclylalkyloxycarbonyl, non-aromatic heterocyclylalkyloxycarbonyl, aromatic carbocyclylalkylamino, non-aromatic carbocyclylalkylamino, aromatic heterocyclylalkylamino, non-aromatic heterocyclylalkylamino, aromatic carbocyclylsulfanyl, non-aromatic carbocyclylsulfanyl, aromatic heterocyclylsulfanyl, non-aromatic heterocyclylsulfanyl, non-aromatic carbocyclylsulfonyl, aromatic carbocyclylsulfonyl, aromatic heterocyclylsulfonyl, non-aromatic heterocyclylsulfonyl, alkylsulfonyloxy, alkenylsulfonyloxy, alkynylsulfonyloxy, non-aromatic carbocyclylsulfonyloxy, aromatic carbocyclylsulfonyloxy, aromatic heterocyclyl sulfonyloxy and non-aromatic heterocyclylsulfonyloxy.

(140) Substituents in the ring of the above substituted or unsubstituted fused aromatic heterocyclyl, substituted or unsubstituted fused aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic heterocyclyl, substituted or unsubstituted non-aromatic heterocyclyl, substituted or unsubstituted non-aromatic carbocyclylcarbonyl, substituted or unsubstituted aromatic carbocyclylcarbonyl, substituted or unsubstituted aromatic heterocyclylcarbonyl, substituted or unsubstituted non-aromatic heterocyclylcarbonyl, substituted or unsubstituted non-aromatic carbocyclylsulfonyl, substituted or unsubstituted aromatic carbocyclylsulfonyl, substituted or unsubstituted aromatic heterocyclylsulfonyl, substituted or unsubstituted non-aromatic heterocyclylsulfonyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, substituted or unsubstituted fused aromatic carbocyclyl, substituted or unsubstituted fused aromatic heterocyclyl, substituted or unsubstituted non-aromatic heterocyclyl, substituted or unsubstituted aromatic carbocyclyloxycarbonyl, substituted or unsubstituted non-aromatic carbocyclyloxycarbonyl, substituted or unsubstituted aromatic heterocyclyloxycarbonyl, substituted or unsubstituted non-aromatic heterocyclyloxycarbonyl, substituted or unsubstituted non-aromatic carbocyclyloxy, substituted or unsubstituted aromatic carbocyclyloxy, substituted or unsubstituted aromatic heterocyclyloxy, substituted or unsubstituted non-aromatic heterocyclyloxy, substituted or unsubstituted non-aromatic carbocyclylsulfanyl, substituted or unsubstituted aromatic carbocyclylsulfanyl, substituted or unsubstituted aromatic heterocyclylsulfanyl, substituted or unsubstituted non-aromatic heterocyclylsulfanyl, substituted or unsubstituted non-aromatic carbocyclylsulfinyl, substituted or unsubstituted aromatic carbocyclylsulfinyl, substituted or unsubstituted aromatic heterocyclyl sulfinyl, substituted or unsubstituted non-aromatic heterocyclyl sulfinyl, substituted or unsubstituted non-aromatic carbocyclylsulfonyloxy, substituted or unsubstituted aromatic carbocyclylsulfonyloxy, substituted or unsubstituted aromatic heterocyclylsulfonyloxy, substituted or unsubstituted non-aromatic heterocyclylsulfonyloxy, substituted or unsubstituted non-aromatic carbocyclylcarbonyloxy, substituted or unsubstituted aromatic carbocyclylcarbonyloxy, substituted or unsubstituted aromatic heterocyclylcarbonyloxy and substituted or unsubstituted non-aromatic heterocyclylcarbonyloxy include the following substituents. Hydrogen atom on the ring at arbitrary position(s) can be substituted with one or more group(s) selected from the following substituents.

(141) Substituent:

(142) alkyl, alkenyl, alkynyl, haloalkyl, haloalkenyl, halogen, hydroxy, carboxy, formyl, formyloxy, carbamoyl, sulfamoyl, sulfanyl, sulfino, sulfo, thioformyl, thiocarboxy, dithiocarboxy, thiocarbamoyl, cyano, nitro, nitroso, azido, hydradiono, ureido, amidino, guanidino, trialkylsilyl, alkyloxy, alkyloxy alkyloxy, alkenyloxy, alkynyloxy, haloalkyloxy, trialkylsilyloxy, cyanoalkyloxy, alkylcarbonyl, haloalkylcarbonyl, carbamoylalkylcarbonyl, alkenylcarbonyl, alkynylcarbonyl, monoalkylamino, dialkylamino, alkylsulfonyl, alkenylsulfonyl, alkynylsulfonyl, monoalkylcarbonylamino, dialkylcarbonylamino, monoalkylsulfonylamino, dialkylsulfonylamino, alkylimino, alkenylimino, alkynylimino, alkylcarbonylimino, alkenylcarbonylimino, alkynylcarbonylimino, alkyloxyimino, alkenyloxyimino, alkynyloxyimino, alkylcarbonyloxy, alkenylcarbonyloxy, alkynylcarbonyloxy, alkyloxycarbonyl, monoalkyloxycarbonylamino, dialkyloxycarbonylamino, alkenyloxycarbonyl, alkynyloxycarbonyl, alkylsulfanyl, alkylcarbonylsulfanyl, alkenylsulfanyl, alkynylsulfanyl, alkylsulfinyl, alkenylsulfinyl, alkynylsulfinyl, monoalkylcarbamoyl, mono(hydroxyalkyl)carbamoyl, dialkylcarbamoyl, hydroxycarbamoyl, cyanocarbamoyl, carboxyalkylcarbamoyl, mono(dialkylaminoalkyl)carbamoyl di(dialkylaminoalkyl)carbamoyl, non-aromatic carbocyclylalkylcarbamoyl, non-aromatic carbocyclylcarbamoyl, non-aromatic heterocyclylalkylcarbamoyl, non-aromatic heterocyclylcarbamoyl, monoalkyloxycarbamoyl, dialkyloxycarbamoyl, monoalkyloxycarbonylalkylcarbamoyl, dialkyloxycarbonylalkylcarbamoyl, monoalkylsulfamoyl, dialkylsulfamoyl, aromatic carbocyclyl, non-aromatic carbocyclyl, aromatic heterocyclyl, non-aromatic heterocyclyl, aromatic carbocyclyloxy, non-aromatic carbocyclyloxy, non-aromatic heterocyclyloxy, non-aromatic heterocyclyloxy, aromatic carbocyclylcarbonyl, non-aromatic carbocyclylcarbonyl, aromatic heterocyclylcarbonyl, non-aromatic heterocyclylcarbonyl, non-aromatic carbocyclylcarbonyloxy, aromatic carbocyclylcarbonyloxy, aromatic heterocyclylcarbonyloxy, non-aromatic heterocyclylcarbonyloxy, aromatic carbocyclyloxycarbonyl, non-aromatic carbocyclyloxycarbonyl, aromatic heterocyclyloxycarbonyl, non-aromatic heterocyclyloxycarbonyl, aromatic carbocyclylalkyl, non-aromatic carbocyclylalkyl, aromatic heterocyclylalkyl, non-aromatic heterocyclylalkyl, aromatic carbocyclylalkyloxy, non-aromatic carbocyclylalkyloxy, aromatic heterocyclylalkyloxy, non-aromatic heterocyclylalkyloxy, aromatic carbocyclylalkyloxycarbonyl, non-aromatic carbocyclylalkyloxycarbonyl, aromatic heterocyclylalkyloxycarbonyl, non-aromatic heterocyclylalkyloxycarbonyl, aromatic carbocyclylalkylamino, non-aromatic carbocyclylalkylamino, aromatic heterocyclylalkylamino, non-aromatic heterocyclylalkylamino, aromatic carbocyclylsulfanyl, non-aromatic carbocyclylsulfanyl, aromatic heterocyclylsulfanyl, non-aromatic heterocyclylsulfanyl, aromatic carbocyclylsulfonyl, non-aromatic carbocyclylsulfonyl, aromatic heterocyclylsulfonyl, non-aromatic heterocyclylsulfonyl, alkylsulfonyloxy, alkenylsulfonyloxy, alkynylsulfonyloxy, non-aromatic carbocyclylsulfonyloxy, aromatic carbocyclylsulfonyloxy, aromatic heterocyclylsulfonyloxy, non-aromatic heterocyclylsulfonyloxy, alkyloxycarbonylalkyl, carboxyalkyl, hydroxyalkyl, dialkylaminoalkyl, hydroxyalkyl, alkyloxyalkyl, aromatic carbocyclylalkyloxyalkyl, non-aromatic carbocyclylalkyloxyalkyl, aromatic heterocyclylalkyloxyalkyl and non-aromatic heterocyclylalkyloxyalkyl.

(143) Preferably, halogen, substituted or unsubstituted alkyl (a substituent group: halogen, hydroxy), substituted or unsubstituted alkenyl (a substituent group: halogen, hydroxy), substituted or unsubstituted alkynyl (a substituent group: halogen, hydroxy), substituted or unsubstituted non-aromatic carbocyclyl (a substituent group: halogen, hydroxy, cyano, alkyl, haloalkyl, aromatic carbocyclyl), substituted or unsubstituted aromatic carbocyclyl (a substituent group: halogen, hydroxy, cyano, alkyl, haloalkyl, aromatic carbocyclyl), substituted or unsubstituted non-aromatic heterocyclyl (a substituent group: halogen, hydroxy, cyano, alkyl, haloalkyl, aromatic carbocyclyl), substituted or unsubstituted aromatic heterocyclyl (a substituent group: halogen, hydroxy, cyano, alkyl, haloalkyl, aromatic carbocyclyl), substituted or unsubstituted alkyloxy (a substituent group: halogen, cyano, non-aromatic carbocyclyl, halo non-aromatic carbocyclyl, cyano non-aromatic carbocyclyl, halo aromatic carbocyclyl, non-aromatic heterocyclyl), substituted or unsubstituted alkenyloxy (a substituent group: halogen, cyano, non-aromatic carbocyclyl, halo non-aromatic carbocyclyl, cyano non-aromatic carbocyclyl, halo aromatic carbocyclyl, non-aromatic heterocyclyl), substituted or unsubstituted alkynyloxy (a substituent group: halogen, cyano, non-aromatic carbocyclyl, halo non-aromatic carbocyclyl, cyano non-aromatic carbocyclyl, halo aromatic carbocyclyl, non-aromatic heterocyclyl), substituted or unsubstituted non-aromatic carbocyclyloxy (a substituent group: cyano, halogen, hydroxy, alkyl, alkyloxy), substituted or unsubstituted aromatic carbocyclyloxy (a substituent group: cyano, halogen, hydroxy, alkyl, alkyloxy), substituted or unsubstituted non-aromatic heterocyclyloxy (a substituent group: cyano, halogen, hydroxy, alkyl, alkyloxy), substituted or unsubstituted aromatic heterocyclyloxy (a substituent group: cyano, halogen, hydroxy, alkyl, alkyloxy), substituted or unsubstituted amino (a substituent group: cyano, alkyl, cyanoalkyl) are exemplified.

(144) More preferably, halogen, alkyl, dihaloalkyl, hydroxyalkyl, halo non-aromatic carbocyclyl, non-aromatic heterocyclyl, halo non-aromatic heterocyclyl, dihalo non-aromatic heterocyclyl, tetrahalo non-aromatic heterocyclyl, hydroxy non-aromatic heterocyclyl, alkyl non-aromatic heterocyclyl, dialkyl non-aromatic heterocyclyl, cyano non-aromatic heterocyclyl, aromatic carbocycle non-aromatic heterocyclyl, alkyloxy, haloalkyloxy, dihaloalkyloxy, trihaloalkyloxy, cyanoalkyloxy, non-aromatic carbocyclylalkyloxy, dihalo non-aromatic carbocyclylalkyloxy, cyano non-aromatic carbocyclylalkyloxy, halo aromatic carbocyclylalkyloxy, non-aromatic heterocyclylalkyloxy, halo non-aromatic heterocyclylalkyloxy, non-aromatic heterocyclyloxyalkyloxy, non-aromatic carbocyclyloxy, cyano non-aromatic carbocyclyloxy, halo non-aromatic carbocyclyloxy, dihalo non-aromatic carbocyclyloxy, methyl non-aromatic carbocyclyloxy, hydroxy non-aromatic carbocyclyloxy, alkyloxy non-aromatic carbocyclyloxy, aromatic carbocyclyloxy, non-aromatic heterocyclyloxy, halo non-aromatic heterocyclyloxy, halo aromatic heterocyclyloxy, dialkylamino, cyanoalkyl, alkyl (cyanoalkyl)amino are exemplified.

(145) The above substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted non-aromatic heterocyclyl, substituted or unsubstituted fused aromatic carbocyclyl and substituted or unsubstituted fused aromatic heterocyclyl can be substituted with oxo. In this case, two hydrogen atoms on the carbon atom are replaced with O group as follows:

(146) ##STR00050##

(147) The non-aromatic carbocycle part and non-aromatic heterocycle part in the above substituted or unsubstituted non-aromatic heterocyclyl, substituted or unsubstituted aromatic carbocyclyloxy, substituted or unsubstituted non-aromatic heterocyclyloxy, substituted or unsubstituted non-aromatic carbocyclylsulfanyl, substituted or unsubstituted non-aromatic heterocyclylsulfanyl, substituted or unsubstituted non-aromatic carbocyclylsulfinyl, substituted or unsubstituted non-aromatic heterocyclyl sulfinyl, substituted or unsubstituted non-aromatic carbocyclylsulfonyl, substituted or unsubstituted non-aromatic heterocyclylsulfonyl, substituted or unsubstituted non-aromatic carbocyclylsulfonyloxy, substituted or unsubstituted non-aromatic heterocyclylsulfonyloxy, substituted or unsubstituted non-aromatic carbocyclylcarbonyl, substituted or unsubstituted non-aromatic heterocyclylcarbonyl, substituted or unsubstituted non-aromatic carbocyclylcarbonyloxy, substituted or unsubstituted non-aromatic heterocyclylcarbonyloxy, substituted or unsubstituted non-aromatic carbocyclyloxycarbonyl and substituted or unsubstituted non-aromatic heterocyclyloxycarbonyl can be substituted with oxo.

(148) Alkylcarbonylsulfanyl means the above alkylcarbonyl bonded to a sulfur atom. For example, methylcarbonylsulfanyl, ethylcarbonylsulfanyl, n-propylcarbonylsulfanyl, isopropylcarbonylsulfanyl, n-butylcarbonylsulfanyl, tert-butylcarbonylsulfanyl, isobutylcarbonylsulfanyl, sec-butylcarbonylsulfanyl, pentylcarbonylsulfanyl, isopentylcarbonylsulfanyl, hexylcarbonylsulfanyl and the like are exemplified. A preferable embodiment of alkylcarbonylsulfanyl includes methylcarbonylsulfanyl, ethylcarbonylsulfanyl, propylcarbonylsulfanyl, isopropylcarbonylsulfanyl, tert-butylcarbonylsulfanyl, isobutylcarbonylsulfanyl, sec-butylcarbonylsulfanyl and the like.

(149) Haloalkyl means the above alkyl the one or more arbitrary hydrogen(s) of which is (are) substituted with the above halogen. For example, monofluoromethyl, monofluoroethyl, monofluoropropyl, 2,2,3,3,3-pentafluoropropyl, monochloromethyl, trifluoromethyl, trichloromethyl, 2,2,2-trifluoroethyl, 2,2,2-trichloroethyl, 1,2-dibromoethyl, 1,1,1-trifluoropropane-2-yl and the like are exemplified.

(150) Haloalkylcarbonyl means the above haloalkyl bonded to a carbonyl group. For example, monofluoromethylcarbonyl, difluoromethylcarbonyl, monofluoroethylcarbonyl, monofluoropropylcarbonyl, 2,2,3,3,3-pentafluoropropylcarbonyl, monochloromethylcarbonyl, trifluoromethylcarbonyl, trichloromethylcarbonyl, 2,2,2-trifluoroethylcarbonyl, 2,2,2-trichloroethylcarbonyl, 1,2-dibromoethylcarbonyl, 1,1,1-trifluoropropane-2-ylcarbonyl and the like are exemplified.

(151) Haloalkenyl means the above alkenyl the one or more arbitrary hydrogen(s) of which is (are) substituted the above halogen.

(152) Hydroxyalkyl means the above alkyl the one or more arbitrary hydrogen(s) of which is (are) substituted with hydroxyl.

(153) Trialkylsilyl means silicon atom bonded to above tree alkyl group. Three alkyl groups may be same or different. For example, trimethylsilyl, triethylsilyl, tert-butyldimethylsilyl, triisopropylsilyl and the like are exemplified.

(154) Trialkylsilyloxy means the above trialkylsilyl bonded to an oxygen atom. For example, trimethylsilyloxy, triethylsilyloxy, tert-butyldimethylsilyloxy, triisopropylsilyloxy and the like are exemplified.

(155) Cyanoalkyl means the above alkyl the one or more arbitrary hydrogen(s) of which is (are) substituted with cyano. For example, cyanomethyl and the like is exemplified.

(156) Cyanoalkyloxy means the above cyanoalkyl bonded to an oxygen atom. For example, cyanomethyloxy and the like are exemplified.

(157) Haloalkyloxy means the above haloalkyl bonded to an oxygen atom. For example, monofluoromethyloxy, monofluoroethyloxy, trifluoromethyloxy, trichloromethyloxy, trifluoroethyloxy, trichloroethyloxy and the like are exemplified. A preferable embodiment of haloalkyloxy includes trifluoromethyloxy, trichloromethyloxy and the like.

(158) Carbamoylalkylcarbonyl means the above alkylcarbonyl substituted with carbamoyl. For example, carbamoylmethylcarbonyl, carbamoylethylcarbonyl and the like are exemplified.

(159) Monoalkylamino means an amino group one hydrogen atom bonded to the nitrogen atom of which is substituted with the above alkyl. Examples of monoalkylamino include methylamino, ethylamino and the like.

(160) Dialkylamino means an amino group two hydrogen atoms bonded to the nitrogen atom of which are substituted with the above alkyl. Two alkyl groups may be same or different. For example, dimethylamino, diethylamino, N,N-diisopropylamino, N-methyl-N-ethylamino, N-isopropyl-N-ethylamino and the like are exemplified.

(161) A preferable embodiment of dialkylamino includes dimethylamino, diethylamino and the like.

(162) Monoalkylcarbonylamino means an amino group one hydrogen atom bonded to the nitrogen atom of which is replaced with the above alkylcarbonyl. For example, methylcarbonylamino, ethylcarbonylamino, propylcarbonylamino, isopropylcarbonylamino, tert-butylcarbonylamino, isobutylcarbonylamino, sec-butylcarbonylamino and the like are exemplified.

(163) A preferable embodiment of monoalkylcarbonylamino includes methylcarbonylamino, ethylcarbonylamino and the like.

(164) Dialkylcarbonylamino means an amino group two hydrogen atoms bonded to the nitrogen atom of which are replaced with the above alkylcarbonyl. Two alkylcarbonyl groups may be same or different. For example, dimethylcarbonylamino, diethylcarbonylamino, N,N-diisopropylcarbonylamino and the like are exemplified. A preferable embodiment of dialkylcarbonylamino includes dimethylcarbonylamino, diethylcarbonylamino and the like.

(165) Monoalkyloxycarbonylamino means an amino group one hydrogen atom bonded to the nitrogen atom of which is replaced with the above alkyloxycarbonyl. A preferable embodiment of monoalkyloxycarbonylamino includes methyloxycarbonylamino, ethyloxycarbonylamino and the like.

(166) Dialkyloxycarbonylamino means an amino group two hydrogen atoms bonded to the nitrogen atom of which are replaced with the above alkyloxycarbonyl. Two alkyloxycarbonyl groups may be same or different.

(167) Monoalkylsulfonylamino means an amino group one hydrogen atom bonded to the nitrogen atom of which is replaced with the above alkylsulfonyl. For example, methylsulfonylamino, ethylsulfonylamino, propylsulfonylamino, isopropylsulfonylamino, tert-butylsulfonylamino, isobutylsulfonylamino, sec-butylsulfonylamino and the like are exemplified.

(168) A preferable embodiment of monoalkylsulfonylamino includes methylsulfonylamino, ethylsulfonylamino and the like.

(169) Dialkylsulfonylamino means an amino group two hydrogen atoms bonded to the nitrogen atom of which are replaced with the above alkylsulfonyl. Two alkylsulfonyl groups may be same or different. For example, dimethylsulfonylamino, diethylsulfonylamino, N,N-diisopropylsulfonylamino and the like are exemplified. A preferable embodiment of dialkylsulfonylamino includes dimethylsulfonylamino, diethylsulfonylamino and the like.

(170) Alkylimino means an imino group a hydrogen atom bonded to the nitrogen atom of which is replaced with the above alkyl. For example, methylimino, ethylimino, n-propylimino, isopropylimino and the like are exemplified.

(171) Alkenylimino means an imino group a hydrogen atom bonded to the nitrogen atom of which is replaced with the above alkenyl. For example, ethylenylimino, propenylimino and the like are exemplified.

(172) Alkynylimino means an imino group a hydrogen atom bonded to the nitrogen atom of which is replaced with the above alkynyl. For example, ethynylimino, propynylimino and the like are exemplified.

(173) Alkylcarbonylimino means an imino group a hydrogen atom bonded to the nitrogen atom of which is replaced with the above alkylcarbonyl. For example, methylcarbonylimino, ethylcarbonylimino, n-propylcarbonylimino, isopropylcarbonylimino and the like are exemplified.

(174) Alkenylcarbonylimino means an imino group a hydrogen atom bonded to the nitrogen atom of which is replaced with the above alkenylcarbonyl. For example, ethylenylcarbonylimino, propenylcarbonylimino and the like are exemplified.

(175) Alkynylcarbonylimino means an imino group a hydrogen atom bonded to the nitrogen atom of which is replaced with the above alkynylcarbonyl. For example, ethynylcarbonylimino, propynylcarbonylimino and the like are exemplified.

(176) Alkyloxyimino means an imino group a hydrogen atom bonded to the nitrogen atom of which is replaced with the above alkyloxy. For example, methyloxyimino, ethyloxyimino, n-propyloxyimino, isopropyloxyimino and the like are exemplified.

(177) Alkenyloxyimino means an imino group a hydrogen atom bonded to the nitrogen atom of which is replaced with the above alkenyloxy. For example, ethylenyloxyimino, propenyloxyimino and the like are exemplified.

(178) Alkynyloxyimino means an imino group a hydrogen atom bonded to the nitrogen atom of which is replaced with the above alkynyloxy. For example, ethynyloxyimino, propynyloxyimino and the like are exemplified.

(179) Monoalkylcarbamoyl means a carbomoyl group a hydrogen atom bonded to the nitrogen atom of which is replaced with the above alkyl. For example, methylcarbamoyl, ethylcarbamoyl and the like are exemplified.

(180) Monoalkylcarbamoylalkyloxy means the above alkyloxy substituted with one or more the above monoalkylcarbamoyl. For example, methylcarbamoylmethyloxy and the like are exemplified.

(181) Mono(hydroxyalkyl)carbamoyl means the above monoalkylcarbamoyl the arbitrary hydrogen atoms of which is replaced with a hydroxyl group. For example, hydroxymethylcarbamoyl, hydroxyethylcarbamoyla and the like are exemplified.

(182) Dialkylcarbamoyl means a carbamoyl group two hydrogen atoms bonded to the nitrogen atom of which are replaced with the above alkyl. Two alkyl groups may be same or different. For example, dimethylcarbamoyl, diethylcarbamoyl and the like are exemplified.

(183) Alkyloxycarbonylalkyl means the above alkyl substituted with one or more the above alkyloxycarbonyl.

(184) Monoalkyloxycarbonylalkylcarbamoyl means a carbamoyl group one hydrogen atom bonded to nitrogen atom of which is replaced with the above alkyloxycarbonylalkyl. For example, methyloxycarbonylmethylcarbamoyl, ethyloxycarbonylmethylcarbamoyl and the like are exemplified.

(185) Dialkyloxycarbonylalkylcarbamoyl means a carbamoyl group two hydrogen atoms bonded to the nitrogen atom of which is replaced with the above alkyloxycarbonylalkyl.

(186) Carboxyalkyl means the above alkyl substituted with one or more above carboxy.

(187) Carboxyalkylcarbamoyl means a carbamoyl group one or more two hydrogen atom(s) bonded to the nitrogen atom of which is (are) replaced with one or more above carboxyalkyl. For example, carboxymethylcarbamoyl and the like are exemplified.

(188) Dialkylaminoalkyl means the above alkyl substituted with one or more above dialkylamino. For example, dimethylaminomethyl, dimethylaminoethyl and the like are exemplified.

(189) Mono(dialkylaminoalkyl)carbamoyl means a carbamoyl group one hydrogen atom bonded to the nitrogen atom of which is replaced with the above dialkylaminoalkyl. For example, dimethylaminomethylcarbamoyl, dimethylaminoethylcarbamoyl and the like are exemplified.

(190) Di(dialkylaminoalkyl)carbamoyl means a carbamoyl group two hydrogen atoms bonded to the nitrogen atom of which are replaced with the above dialkylaminoalkyl. For example, di(methyloxycarbonylmethyl)carbamoyl, di(ethyloxycarbonylmethyl)carbamoyl and the like are exemplified.

(191) Non-aromatic carbocyclylcarbamoyl means a carbamoyl group the hydrogen atom bonded to nitrogen atom of which is replaced with one or more above non-aromatic carbocyclyl. For example, cyclopropylcarbamoyl and the like are exemplified.

(192) Non-aromatic heterocyclylcarbamoyl means a carbamoyl group the hydrogen atom bonded to nitrogen atom of which is replaced with one or more above non-aromatic heterocyclyl. Examples include a group represented by the following Formula:

(193) ##STR00051##

(194) Monoalkyloxycarbamoyl means a carbamoyl group one hydrogen atom bonded to the nitrogen atom of which is replaced with the above alkyloxy. For example, methyloxycarbamoyl and the like are exemplified.

(195) Dialkyloxycarbamoyl means a carbomoyl group two hydrogen atoms bonded to the nitrogen of which are replaced with the above alkyloxy. For example, di(methyloxy)carbamoyl and the like are exemplified.

(196) Monoalkylsulfamoyl means a sulfamoyl group one hydrogen atom bonded to nitrogen atom of which is replaced with the above alkyl. For example, methylsulfamoyl, dimethylsulfamoyl and the like are exemplified.

(197) Dialkylsulfamoyl means a sulfamoyl group two hydrogen atoms bonded to the nitrogen atom of which are replaced with the above alkyl. Two alkyl groups may be same or different. For example, dimethylsulfamoyl, diethylsulfamoyl and the like are exemplified.

(198) Aromatic carbocyclylalkyl means the above alkyl substituted with one or more above aromatic carbocyclyl. For example, benzyl, phenethyl, phenylpropyl, benzhydryl, trityl, naphthylmethyl, a group represented by the following formula:

(199) ##STR00052##
and the like are exemplified.

(200) A preferable embodiment of aromatic carbocyclylalkyl includes benzyl, phenethyl, benzhydryl and the like.

(201) Cycloalkylalkyl means the above alkyl substituted with one or more above cycloalkyl. Cycloalkylalkyl includes cycloalkylalkyl which the alkyl part is further substituted with the above aromatic carbocyclyl. For example, cyclopentylmethyl, cyclohexylmethyl, a group represented by the following formula:

(202) ##STR00053##
and the like are exemplified.

(203) Cycloalkenylalkyl means the above alkyl substituted with one or more above cycloalkenyl. Cycloalkenylalkyl includes Cycloalkenylalkyl which the alkyl part is further substituted with the above aromatic carbocyclyl. For example, cyclopropenylmethyl, cyclobutenylmethyl, cyclopentenylmethyl, cyclohexenylmethyl, and the like are exemplified.

(204) Aromatic heterocyclylalkyl means the above alkyl substituted with one or more above aromatic carbocyclyl. Aromatic heterocyclylalkyl includes Aromatic heterocyclylalkyl which the alkyl part is further substituted with the above aromatic carbocyclyl and/or non-aromatic carbocyclyl. For example, pyridylmethyl, furanylmethyl, imidazolylmethyl, indolylmethyl, benzothiophenylmethyl, oxazolylmethyl, isoxazolylmethyl, thiazolylmethyl, isothiazolylmethyl, pyrazolylmethyl, isopyrazolylmethyl, pyrrolidinylmethyl, benzoxazolylmethyl, a group represented by the following formula:

(205) ##STR00054##
and the like are exemplified.

(206) Non-aromatic heterocyclylalkyl means the above alkyl substituted with one or more above non-aromatic heterocyclyl. Non-aromatic heterocyclylalkyl includes non-aromatic heterocyclylalkyl which the alkyl part is further substituted with the above aromatic carbocyclyl, non-aromatic carbocyclyl and/or aromatic heterocyclyl. For example, tetrahydropyranylmethyl, morpholinylethyl, piperidinylmethyl, piperazinylmethyl, a group represented by the following formula:

(207) ##STR00055##
and the like are exemplified.

(208) Non-aromatic heterocyclylalkylcarbamoyl means a carbamoyl group one or two hydrogen atom(s) bonded to nitrogen atom of which is replaced with one or two above non-aromatic heterocyclylalkyl. For example, a group represented by the following formula is exemplified:

(209) ##STR00056##

(210) Aromatic carbocyclylalkyloxy means the above alkyloxy substituted with one or more above aromatic carbocycle. For example, benzyloxy, phenethyloxy, phenylpropynyloxy, benzhydryloxy, trityloxy, naphthylmethyloxy, a group represented by the following formula:

(211) ##STR00057##
and the like are exemplified.

(212) Non-aromatic carbocyclylalkyloxy means the above alkyloxy substituted with one or more above non-aromatic carbocyclyl. Non-aromatic carbocyclylalkyloxy includes non-aromatic carbocyclylalkyloxy which the alkyl part are further substituted with the above aromatic carbocyclyl. For example, cyclopeopylmethyloxy, cyclobutylmethyloxy, cyclopenthylmethyloxy, cyclohexylmethyloxy, cyclopropylmethyloxy, cyclobutylmethyloxy, cyclopenthylmethyloxy, cyclohexylmethyloxy, a group represented by the following formula:

(213) ##STR00058##
and the like are exemplified.

(214) Aromatic heterocyclylalkyloxy means the above alkyloxy substituted with one or more above aromatic heterocyclyl. Aromatic heterocyclylalkyloxy includes aromatic heterocyclylalkyloxy which the alkyl part is further substituted with the above aromatic carbocyclyl and/or non-aromatic carbocyclyl. For example, pyridylmethyloxy, furanylmethyloxy, imidazolylmethyloxy, indolylmethyloxy, benzothiophenylmethyloxy, oxazolylmethyloxy, isoxazolylmethyloxy, thiazolylmethyloxy, isothiazolylmethyloxy, pyrazolylmethyloxy, isopyrazolylmethyloxy, pyrrolidinylmethyloxy, benzoxazolylmethyloxy, a group represented by the following formula:

(215) ##STR00059##
and the like are exemplified.

(216) Non-aromatic heterocyclylalkyloxy means the above alkyloxy substituted with one or more above non-aromatic heterocyclyl. Non-aromatic heterocyclylalkyloxy includes non-aromatic heterocyclylalkyloxy which the alkyl part is further substituted with the above aromatic carbocyclyl, non-aromatic carbocyclyl and/or aromatic heterocyclyl. For example, tetrahydropyranylmethyloxy, morpholinylethyloxy, piperidinylmethyloxy, piperazinylmethyloxy, a group represented by the following formula:

(217) ##STR00060##
and the like are exemplified.

(218) Aromatic carbocyclylalkyloxycarbonyl means the above alkyloxycarbonyl substituted with one or more above aromatic carbocyclyl. For example, benzyloxycarbonyl, phenethyloxycarbonyl, phenylpropynyloxycarbonyl, benzhydryloxycarbonyl, trityloxycarbonyl, naphthylmethyloxycarbonyl, a group represented by the following formula:

(219) ##STR00061##
and the like are exemplified.

(220) Non-aromatic carbocyclylalkyloxycarbonyl means the above alkyloxycarbonyl substituted with one or more above non-aromatic carbocyclyl. Non-aromatic carbocyclylalkyloxycarbonyl includes non-aromatic carbocyclylalkyloxycarbonyl which the alkyl part is further substituted with the above aromatic carbocyclyl. For example, cyclopropylmethyloxycarbonyl, cyclobutylmethyloxycarbonyl, cyclopentylmethyloxycarbonyl, cyclohexylmethyloxycarbonyl, cyclopropenylmethyloxycarbonyl, cyclobutenylmethyloxycarbonyl, cyclopentenylmethyloxycarbonyl, cyclohexenylmethyloxycarbonyl, a group represented by the following formula:

(221) ##STR00062##
and the like are exemplified.

(222) Aromatic heterocyclylalkyloxycarbonyl means the above alkyloxycarbonyl substituted with one or more above aromatic heterocyclyl. Aromatic heterocyclylalkyloxycarbonyl includes aromatic heterocyclylalkyloxycarbonyl which the alkyl part is further substituted with the above aromatic carbocyclyl and/or non-aromatic carbocyclyl. For example, pyridylmethyloxycarbonyl, furanylmethyloxycarbonyl, imidazolylmethyloxycarbonyl, indolylmethyloxycarbonyl, benzothiophenylmethyloxycarbonyl, oxazolylmethyloxycarbonyl, isoxazolylmethyloxycarbonyl, thiazolylmethyloxycarbonyl, isothiazolylmethyloxycarbonyl, pyrazolylmethyloxycarbonyl, isopyrazolylmethyloxycarbonyl, pyrrolidinylmethyloxycarbonyl, benzoxazolylmethyloxycarbonyl, a group represented by the following formula:

(223) ##STR00063##
and the like are exemplified.

(224) Non-aromatic heterocyclylalkyloxycarbonyl means the above alkyloxycarbonyl substituted with one or more above non-aromatic heterocyclyl. Non-aromatic heterocyclylalkyloxycarbonyl includes non-aromatic heterocyclylalkyloxycarbonyl which the alkyl part is further substituted with the above aromatic carbocyclyl, non-aromatic carbocyclyl and/or aromatic heterocycle. For example, tetrahydropyranylmethyloxy, morpholinylethyloxy, piperidinylmethyloxy, piperazinylmethyloxy, a group represented by the following formula:

(225) ##STR00064##
and the like are exemplified.

(226) Aromatic carbocyclylalkylamino means an amino group one or two hydrogen atom(s) bonded to the nitrogen atom of which is (are) replaced with the above aromatic carbocyclylalkyl. For example, benzylamino, phenethylamino, phenylpropynylamino, benzhydrylamino, tritylamino, naphthylmethylamino, dibenzylamino and the like are exemplified.

(227) Non-aromatic carbocyclylalkylamino means an amino group one or two hydrogen atom(s) bonded to the nitrogen atom of which is (are) replaced with the above non-aromatic carbocyclylalkyl. For example, cyclopropylmethylamino, cyclobutylmethylamino, cyclopentylmethylamino, cyclohexylmethylamino, cyclopropenylmethylamino, cyclobutenylmethylamino, cyclopentenylmethylamino, cyclohexenylmethylamino and the like are exemplified.

(228) Aromatic heterocyclylalkylamino means an amino group one or two hydrogen atom(s) bonded to the nitrogen atom of which is (are) replaced with the above aromatic heterocyclylalkyl. For example, pyridylmethylamino, franylmethylamino, imidazolylmethylamino, indolylmethylamino, benzothiophenylmethylamino, oxazolylmethylamino, isoxazolylmethylamino, thiazolylmethylamino, isothiazolylmethylamino, pyrazolylmethylamino, isopyrazolylmethylamino, pyrrolidinylmethylamino, benzoxazolylmethylamino and the like are exemplified.

(229) Non-aromatic heterocyclylalkylamino means an amino group one or two hydrogen atom(s) bonded to the nitrogen atom of which is (are) replaced with the above non-aromatic heterocyclylalkyl. For example, tetrahydropyranylmethylamino, morpholinylethylamino, piperidinylmethylamino, piperazinylmethylamino and the like are exemplified.

(230) Alkyloxyalkyl means the above alkyl substituted with one or two above alkyloxy. For example, methyloxymethyl, methyloxyethyl, ethyloxymethyl and the like are exemplified.

(231) Aromatic carbocyclylalkyloxyalkyl means the above alkyloxyalkyl substituted with one or more above aromatic carbocyclyl. For example, benzyloxymethyl, phenethyloxymethyl, phenylpropynyloxymethyl, benzhydryloxymethyl, trityloxymethyl, naphthylmethyloxymethyl, a group represented by the following formula:

(232) ##STR00065##
and the like are exemplified.

(233) Non-aromatic carbocyclylalkyloxyalkyl means the above alkyloxyalkyl substituted with one or more above non-aromatic carbocyclyl. Non-aromatic carbocyclylalkyloxyalkyl includes non-aromatic carbocyclylalkyloxyalkyl which the alkyl part bonded to the non-aromatic heterocycle is further substituted with the above aromatic carbocyclyl. For example, cyclopropylmethyloxymethyl, cyclobutylmethyloxymethyl, cyclopentylmethyloxymethyl, cyclohexylmethyloxymethyl, cyclopropenylmethyloxymethyl, cyclobutenylmethyloxymethyl, cyclopentenylmethyloxymethyl, cyclohexenylmethyloxymethyl, groups represented by the following formula:

(234) ##STR00066##
and the like are exemplified.

(235) Aromatic heterocyclylalkyloxyalkyl means the above alkyloxyalkyl substituted with one or more above aromatic heterocyclyl. Aromatic heterocyclylalkyloxyalkyl includes aromatic heterocyclylalkyloxyalkyl which the alkyl part bonded to the aromatic heterocycle is further substituted with the above aromatic carbocyclyl and/or non-aromatic carbocyclyl. For example, pyridylmethyloxymethyl, franylmethyloxymethyl, imidazolylmethyloxymethyl, indolylmethyloxymethyl, benzothiophenylmethyloxymethyl, oxazolylmethyloxymethyl, isoxazolylmethyloxymethyl, thiazolylmethyloxymethyl, isothiazolylmethyloxymethyl, pyrazolylmethyloxymethyl, isopyrazolylmethyloxymethyl, pyrrolidinylmethyloxymethyl, benzoxazolylmethyloxymethyl, groups represented by the following formula:

(236) ##STR00067##
and the like are exemplified.

(237) Non-aromatic heterocyclylalkyloxyalkyl means the above alkyloxyalkyl substituted with one or more above non-aromatic heterocyclyl. Non-aromatic heterocyclylalkyloxyalkyl includes non-aromatic heterocyclylalkyloxyalkyl which the alkyl part bonded to the non-aromatic heterocycle is further substituted with the above aromatic carbocyclyl, non-aromatic carbocyclyl and/or aromatic heterocyclyl. For example, tetrahydropyranylmethyloxymethyl, morpholinylethyloxymethyl, piperidinylmethyloxymethyl, piperazinylmethyloxymethyl, groups represented by the following formula:

(238) ##STR00068##
and the like are exemplified.

(239) Alkyloxyalkyloxy means the above alkyloxyalkyl bonded to an oxygen atom.

(240) Preferable embodiments of R.sup.1, R.sup.2, R.sup.3, R.sup.4, -L.sup.1-, -L.sup.2- and ring A in the compounds of formula (I) are described below.

(241) ##STR00069##
The following possible combinatorial compounds are preferable.

(242) R.sup.1 includes substituted or unsubstituted fused aromatic heterocyclyl, substituted or unsubstituted fused aromatic carbocyclyl, substituted or unsubstituted non-aromatic heterocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, a group represented by Formula:

(243) ##STR00070##
or substituted or unsubstituted 5-membered aromatic heterocyclyl, X.sup.1 is N or C(R.sup.x1), X.sup.2 is N or C(R.sup.x2), X.sup.3 is N or C(R.sup.x3), X.sup.4 is N or C(R.sup.x4), R.sup.x1, R.sup.x2, R.sup.x3, and R.sup.x4 include each independently hydrogen, halogen, hydroxy, carboxy, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkenyloxy, substituted or unsubstituted alkynyloxy, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkenylsulfanyl, substituted or unsubstituted alkynylsulfanyl, substituted or unsubstituted amino, substituted or unsubstituted carbamoyl, substituted or unsubstituted sulfamoyl, substituted or unsubstituted alkylcarbonyl, substituted or unsubstituted alkenylcarbonyl, substituted or unsubstituted alkynylcarbonyl, substituted or unsubstituted alkyloxycarbonyl, substituted or unsubstituted alkenyloxycarbonyl, substituted or unsubstituted alkynyloxycarbonyl or substituted or unsubstituted sulfamoyl, R.sup.x5 includes halogen, hydroxy, carboxy, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkenyloxy, substituted or unsubstituted alkynyloxy, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkenylsulfanyl, substituted or unsubstituted alkynylsulfanyl, substituted or unsubstituted amino, substituted or unsubstituted carbamoyl, substituted or unsubstituted alkylcarbonyl, substituted or unsubstituted alkenylcarbonyl, substituted or unsubstituted alkynylcarbonyl, substituted or unsubstituted alkyloxycarbonyl, substituted or unsubstituted alkenyloxycarbonyl, substituted or unsubstituted alkynyloxycarbonyl or substituted or unsubstituted sulfamoyl.

(244) A preferable embodiment of R.sup.1 includes substituted or unsubstituted benzothiazolyl, substituted or unsubstituted benzoxazolyl, substituted or unsubstituted benzimidazolyl, substituted or unsubstituted indolyl, substituted or unsubstituted indazolyl, substituted or unsubstituted isoquinolyl, substituted or unsubstituted quinoxalinyl, substituted or unsubstituted naphtalenyl, substituted or unsubstituted aziridinyl, substituted or unsubstituted oxyranyl, substituted or unsubstituted thiiranyl, substituted or unsubstituted azetidinyl, substituted or unsubstituted oxetanyl, substituted or unsubstituted thietanyl, substituted or unsubstituted pyrrolidinyl, substituted or unsubstituted tetrahydrofuranyl, substituted or unsubstituted tetrahydrothiophenyl, substituted or unsubstituted piperidinyl, substituted or unsubstituted piperidino, substituted or unsubstituted tetrahydropyranyl, substituted or unsubstituted tetrahydropyranyl, substituted or unsubstituted piperazinyl, substituted or unsubstituted morpholinyl, substituted or unsubstituted morpholino, substituted or unsubstituted thiomorpholinyl, substituted or unsubstituted thiomorpholino, substituted or unsubstituted cyclobutanyl, the groups represented by Formula:

(245) ##STR00071##
or substituted or unsubstituted 5-membered aromatic heterocyclyl.

(246) Another preferable embodiment of R.sup.1 includes substituted or unsubstituted naphtalenyl, substituted or unsubstituted pyrimidinyl, substituted or unsubstituted dihydroindenyl, substituted or unsubstituted dihydrobenzofuranyl, substituted or unsubstituted indolinyl, substituted or unsubstituted tetrahydroisoquinolinyl, substituted or unsubstituted benzoxazolyl, substituted or unsubstituted benzothiazolyl, substituted or unsubstituted benzopyrazolyl, substituted or unsubstituted benzoisothiazolyl or substituted or unsubstituted oxazolinyl and the like.

(247) Furthermore, another preferable embodiment of R.sup.1 includes substituted or unsubstituted naphtalenyl, substituted or unsubstituted dihydroindenyl, substituted or unsubstituted dihydrobenzofuranyl, substituted or unsubstituted indolinyl, substituted or unsubstituted tetrahydroisoquinolinyl, substituted or unsubstituted benzoxazolyl, substituted or unsubstituted benzothiazolyl, substituted or unsubstituted benzopyrazolyl, substituted or unsubstituted benzoisothiazolyl, substituted or unsubstituted oxazolinyl or the group represented by Formula:

(248) ##STR00072##

(249) Furthermore, another preferable embodiment of R.sup.1 includes substituted or unsubstituted benzothiazolyl, substituted or unsubstituted benzoxazolyl, substituted or unsubstituted benzoimidazolyl, substituted or unsubstituted benzopyrazolyl, substituted or unsubstituted thiazolopyridinyl, substituted or unsubstituted indolyl, substituted or unsubstituted indazolyl, substituted or unsubstituted isoquinolyl, substituted or unsubstituted quinazolinyl or substituted or unsubstituted quinoxalinyl.

(250) In the above formula, R.sup.x1, R.sup.x2, R.sup.x3, and R.sup.x4 include each independently hydrogen, halogen, hydroxy, carboxy, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkenyloxy, substituted or unsubstituted alkynyloxy, substituted or unsubstituted alkyl sulfanyl, substituted or unsubstituted alkenylsulfanyl, substituted or unsubstituted alkynylsulfanyl, substituted or unsubstituted amino, substituted or unsubstituted carbamoyl, substituted or unsubstituted sulfamoyl, substituted or unsubstituted alkylcarbonyl, substituted or unsubstituted alkenylcarbonyl, substituted or unsubstituted alkynylcarbonyl, substituted or unsubstituted alkyloxycarbonyl, substituted or unsubstituted alkenyloxycarbonyl, substituted or unsubstituted alkynyloxycarbonyl or substituted or unsubstituted sulfamoyl.

(251) A preferable embodiment of R.sup.x1, R.sup.x2, R.sup.x3, and R.sup.x4 include each independently hydrogen, halogen, hydroxy, carboxy, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted amino, substituted or unsubstituted carbamoyl, substituted or unsubstituted alkylcarbonyl, substituted or unsubstituted alkyloxycarbonyl or substituted or unsubstituted sulfamoyl.

(252) Another preferable embodiment of R.sup.x1, R.sup.x2, R.sup.x3, and R.sup.x4 include hydrogen, halogen, cyano or substituted or unsubstituted alkyl.

(253) R.sup.x5 includes halogen, hydroxy, carboxy, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkenyloxy, substituted or unsubstituted alkynyloxy, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkenylsulfanyl, substituted or unsubstituted alkynylsulfanyl, substituted or unsubstituted amino, substituted or unsubstituted carbamoyl, substituted or unsubstituted alkylcarbonyl, substituted or unsubstituted alkenylcarbonyl, substituted or unsubstituted alkynylcarbonyl, substituted or unsubstituted alkyloxycarbonyl, substituted or unsubstituted alkenyloxycarbonyl, substituted or unsubstituted alkynyloxycarbonyl or substituted or unsubstituted sulfamoyl.

(254) Another preferable embodiment of R.sup.x5 includes halogen, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted amino, substituted or unsubstituted carbamoyl, substituted or unsubstituted alkylcarbonyl, substituted or unsubstituted alkyloxycarbonyl or substituted or unsubstituted sulfamoyl.

(255) Another preferable embodiment of R.sup.x5 includes halogen, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted amino, substituted or unsubstituted carbamoyl or substituted or unsubstituted alkylcarbonyl.

(256) Furthermore, another preferable embodiment of R.sup.1 includes the groups represented by Formula:

(257) ##STR00073##

(258) In the above formula, a preferable embodiment of R.sup.1a, R.sup.1b, R.sup.1c, R.sup.1d and R.sup.1e includes each independently hydrogen, halogen, hydroxy, carboxy, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkenyloxy, substituted or unsubstituted alkynyloxy, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkenylsulfanyl, substituted or unsubstituted alkynylsulfanyl, substituted or unsubstituted amino, substituted or unsubstituted carbamoyl, substituted or unsubstituted sulfamoyl, substituted or unsubstituted alkylcarbonyl, substituted or unsubstituted alkenylcarbonyl, substituted or unsubstituted alkynylcarbonyl, substituted or unsubstituted alkyloxycarbonyl, substituted or unsubstituted alkenyloxycarbonyl or substituted or unsubstituted alkynyloxycarbonyl.

(259) More preferably, R.sup.1a, R.sup.1b, R.sup.1c, R.sup.1d and R.sup.1e include each independently hydrogen, halogen, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted amino, substituted or unsubstituted carbamoyl, substituted or unsubstituted sulfamoyl, substituted or unsubstituted alkylcarbonyl or substituted or unsubstituted alkyloxycarbonyl.

(260) Especially, preferable examples include each independently hydrogen, halogen, cyano, substituted or unsubstituted alkyl or substituted or unsubstituted alkyoxy.

(261) A preferable embodiment of R.sup.1a includes substituted or unsubstituted alkyl or substituted or unsubstituted alkyloxy.

(262) In the above formula, a preferable embodiment of R.sup.1f includes hydrogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkylcarbonyl, substituted or unsubstituted alkenylcarbonyl or substituted or unsubstituted alkynylcarbonyl, more preferably hydrogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkylcarbonyl.

(263) R.sup.2 includes substituted or unsubstituted alkyl.

(264) A preferable embodiment of R.sup.2 includes methyl or hydroxymethyl.

(265) R.sup.3 includes hydrogen or substituted or unsubstituted alkyl.

(266) A preferable embodiment of R.sup.3 includes hydrogen.

(267) R.sup.4 includes substituted or unsubstituted alkylcarbonyl, substituted or unsubstituted alkenylcarbonyl, substituted or unsubstituted alkynylcarbonyl, substituted or unsubstituted non-aromatic carbocyclylcarbonyl, substituted or unsubstituted aromatic carbocyclylcarbonyl, substituted or unsubstituted non-aromatic heterocyclylcarbonyl, substituted or unsubstituted aromatic heterocyclylcarbonyl, substituted or unsubstituted alkyloxycarbonyl, substituted or unsubstituted alkenyloxycarbonyl, substituted or unsubstituted alkynyloxycarbonyl, substituted or unsubstituted non-aromatic carbocyclyloxycarbonyl, substituted or unsubstituted aromatic carbocyclyloxycarbonyl, substituted or unsubstituted non-aromatic heterocyclyloxycarbonyl, substituted or unsubstituted aromatic heterocyclyloxycarbonyl or substituted or unsubstituted carbamoyl.

(268) A preferable embodiment of R.sup.4 includes substituted or unsubstituted alkylcarbonyl, substituted or unsubstituted alkenylcarbonyl, substituted or unsubstituted alkynylcarbonyl, substituted or unsubstituted alkyloxycarbonyl, substituted or unsubstituted alkenyloxycarbonyl, substituted or unsubstituted alkynyloxycarbonyl or substituted or unsubstituted carbamoyl.

(269) Another preferable embodiment of R.sup.4 includes substituted or unsubstituted alkylcarbonyl, substituted or unsubstituted alkyloxycarbonyl or substituted or unsubstituted carbamoyl.

(270) -L.sup.1- includes O(CR.sup.6R.sup.7)m-.

(271) A preferable embodiment of -L.sup.1- includes O or OCH.sub.2.

(272) Another preferable embodiment of -L.sup.1- includes O.

(273) -L.sup.2- includes O(CR.sup.6R.sup.7)n- or C(O)(CR.sup.6R.sup.7)n-.

(274) A preferable embodiment of -L.sup.2- includes OCH.sub.2, OCH(CH.sub.3), OCH.sub.2CH.sub.2 or C(O)(CH.sub.2).

(275) Another preferable embodiment of -L.sup.2- includes OCH.sub.2, OCH(CH.sub.3) or OCH.sub.2CH.sub.2.

(276) Another preferable embodiment of -L.sup.2- includes OCH.sub.2 or OCH(CH.sub.3).

(277) Each R.sup.6 is independently hydrogen, halogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl or substituted or unsubstituted alkynyl.

(278) A preferable embodiment of R.sup.6 includes hydrogen, halogen or substituted or unsubstituted alkyl.

(279) Another preferable embodiment of R.sup.6 includes hydrogen or substituted or unsubstituted alkyl.

(280) Each R.sup.7 is independently hydrogen, halogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl or substituted or unsubstituted alkynyl.

(281) A preferable embodiment of R.sup.7 includes hydrogen, halogen or substituted or unsubstituted alkyl.

(282) Another preferable embodiment of R.sup.7 includes hydrogen or substituted or unsubstituted alkyl.

(283) A preferable embodiment of the ring which is formed by R.sup.2 taken together with either R.sup.6 or R.sup.7 includes cyclobutane, cyclopentane, cyclohexane, oxetane, tetrahydrofuran, tetrahydropyran, azetidine, piperidine, piperazine or morpholine.

(284) Another preferable embodiment of the ring which is formed by R.sup.2 taken together with either R.sup.6 or R.sup.7 includes cyclobutane, cyclopentane or cyclohexane.

(285) A preferable embodiment of n includes 1.

(286) A preferable embodiment of m includes 0 or 1.

(287) Another preferable embodiment of m includes 0.

(288) A preferable embodiment of the group represented by Formula:

(289) ##STR00074##
includes the group represented by Formula:

(290) ##STR00075##

(291) Ring A includes substituted or unsubstituted benzene, substituted or unsubstituted 4- to 6-membered non-aromatic carbocycle, substituted or unsubstituted 5- to 6-membered aromatic heterocycle or substituted or unsubstituted 4- to 6-membered non-aromatic heterocycle.

(292) A preferable embodiment of ring A includes substituted or unsubstituted cyclobutane, substituted or unsubstituted cyclopentane, substituted or unsubstituted azetidine, substituted or unsubstituted oxetane, substituted or unsubstituted thietane, substituted or unsubstituted pyrrolidine, substituted or unsubstituted tetrahydrofuran, substituted or unsubstituted thiorane, substituted or unsubstituted piperidine, substituted or unsubstituted molpholine, substituted or unsubstituted tetrahydropyran, substituted or unsubstituted tetrahydrothiopyran, substituted or unsubstituted pyrrole, substituted or unsubstituted furan, substituted or unsubstituted thiophene, substituted or unsubstituted imidazole, substituted or unsubstituted pyrazole, substituted or unsubstituted oxazole, substituted or unsubstituted isoxazole, substituted or unsubstituted thiazole, substituted or unsubstituted isothiazole, substituted or unsubstituted oxadiazole, substituted or unsubstituted thiadiazole, substituted or unsubstituted pyridine, substituted or unsubstituted pyrimidine, substituted or unsubstituted pyrazine or substituted or unsubstituted pyridazine.

(293) Another preferable embodiment of ring A includes substituted or unsubstituted cyclobutane, substituted or unsubstituted cyclopentane, substituted or unsubstituted cyclohexaneubstituted or unsubstituted benzene, substituted or unsubstituted piperidine, substituted or unsubstituted pyridine, substituted or unsubstituted pyrazine, substituted or unsubstituted pyrimidine or substituted or unsubstituted thiazole.

(294) Another preferable embodiment of ring A includes cyclobutane, cyclohexane, benzene, piperidine, pyrazine, pyrimidine or thiazole.

(295) A disease associated with ACC2 includes metabolic syndrome, obesity, diabetes, insulin resistance, abnormal glucose tolerance, diabetic peripheral neuropathy, diabetic nephropathy, diabetic retinal disease, diabetic macroangiopathy, hyperlipidemia, hypertension, cardiovascular illness, arterial sclerosis, atherosclerotic cardiovascular disease, cardiac arrest, cardiac infarction, infectious disease, neoplasm and the like.

(296) The compound of formula (I) and (I) are not limited to the specific isomer, include all possible isomers (for example, keto-enol isomer, imine-enamine isomer, diastereo isomer, enantiomer, rotamer and the like) and racemates or thereof, with the exception of a part represented by the chemical structure.

(297) One or more hydrogen, carbon and/or other atoms of the compounds of formula (I) and (I) can be replaced by an isotope of the hydrogen, carbon, and/or other atoms. The examples of isotopes include isotopes of hydrogen, carbon, nitrogen, oxygen, phosphorous, sulfur, fluorine and chloride, such as .sup.2H, .sup.3H, .sup.11C, .sup.13C, .sup.14C, .sup.15N, .sup.18O, .sup.17O, .sup.31P, .sup.32P, .sup.35S, .sup.18F, .sup.123I and .sup.36Cl, respectively. The compounds of formula (I) and (I) include compounds that substituted with the isotopes. And the compounds substituted with the isotopes are useful as medicine, and include radiolabeled forms of the compounds of formula (I) and (I) radiolabeled, radiolabeled form. The process for radiolabeling the compounds thereof to prepare the radiolabeled form is encompassed by the invention, is useful as a research and/or diagnostic tool in metabolism pharmacokinetic studies and in binding assays.

(298) Radiolabeled compounds of formula (I) and (I) can be prepared by methods known in the art. For example, tritiated compounds of formula (I) and (I) can be prepared by introducing tritium into the particular compound of formula ((I) and (I), for example, by catalytic dehalogenation with tritium. This method may include reacting a suitably halogen-substituted precursor of a compound of formula (I) and (I) with tritium gas in the presence of a suitable catalyst such as Pd/C, in the presence or absence of a base. Other suitable methods for preparing tritiated compounds can be found in Filer, Isotopes in the Physical and Biomedical Sciences, Vol. 1, Labeled Compounds (Part A), Chapter 6 (1987). .sup.14C-labeled compounds can be prepared by employing materials having a .sup.14C carbon.

(299) Examples of pharmaceutically acceptable salts include salt such as a compound of formula (I) and (I) with alkaline metals (e.g.: lithium, sodium, potassium etc.), alkaline earth metals (e.g., calcium, barium etc.), magnesium, transition metals (e.g. zinc, iron etc.), ammonium, organic bases (e.g. trimethylamine, triethylamine, dicyclohexylamine, ethanolamine, diethanolamine, triethanolamine, meglumine, diethanolamine, ethylenediamine, pyridine, picoline, quinolone etc.) and amino acids, and salts with inorganic acids (e.g. hydrocholoric, sulfuric acid, nitric acid, carbonic acids, hydrobromic acid, phosphoric acid, hydroiodic acid etc.), or organic acids (e.g. formic acid, acetic acid, propionic acid, trifluoroacetic acid, citric acid, lactic acid, tartaric acid, oxalic acid, maleic acid, fumaric acid, maldelic acid, glutaric acid, malic acid, benzoic acid, phthalic acid, ascorbic acid, benzenesulfonic acid, p-toluenesulfonic acid, methanesulfonic acid, ethanesulfonic acid etc.). Especially, preferable examples are salts with hydrochloric acid, sulfuric acid, phosphoric acid, tartaric acid, or methanesulfonic acid. These salts may be formed by a routine method.

(300) The compounds of the invention of formula (I) and (I) or its pharmaceutically acceptable salts can be prepared in a form of solvate thereof (for example, hydrate etc.) and/or its crystal polymorph, the present invention includes such solvate and polymorph. Any number of solvent molecules can be coordinated to form such solvate to the compounds of formula (I) and (I). When the compounds of formula (I) and (I) or its pharmaceutically acceptable salt are left in the atmosphere, its can absorb moisture to attach the absorbed water or to form the hydrate. Also, the compounds of formula (I) and (I) or its pharmaceutically acceptable salt can be recrystallized to form the crystal polymorph.

(301) The compounds of the invention of formula (I) and (I) or its pharmaceutically acceptable salts can be formed the prodrug, the present invention includes the various prodrug. The prodrug is the derivatives of the compounds for this invention having the group decomposed by chemical or metabolic method, and are compounds that prepared by solvolysis or under condition, and are compounds having an activity in vivo. The prodrug includes compounds converted to the compounds for this invention of formula (I) and (I) by oxidation, reduction or hydrolysis under physiological conditions in vivo and compounds hydrolyzed to the compounds for this invention of formula (I) and (I) by gastric acid and the like. The methods for selecting suitable prodrug derivatives and preparing thereof can be found in filer, for example, Design of Prodrugs, Elsevier, Amsterdam 1985. The prodrug may have an activity in its own.

(302) When the compounds of the invention of formula (I) and (I) or its pharmaceutically acceptable salt has hydroxy, for example, it is reacted with the suitable acyl halide, the suitable acid anhydride, the suitable sulfonyl chloride, the suitable sulfonyl anhydride and mixed anhydride or with condensation agent to afford the prodrug such as the acyloxy derivatives or sulfonyloxy derivatives.

(303) Examples of the prodrug are CH.sub.3COO, C.sub.2H.sub.5COO, t-BuCOO, C.sub.15H.sub.31COO, PhCOO, (m-NaOOCPh)COO, NaOOCCH.sub.2CH.sub.2COO, CH.sub.3CH(NH.sub.2)COO, CH.sub.2N(CH.sub.3).sub.2COO, CH.sub.3SO.sub.3, CH.sub.3CH.sub.2SO.sub.3, CF.sub.3SO.sub.3, CH.sub.2FSO.sub.3, CF.sub.3CH.sub.2SO.sub.3, p-CH.sub.3O-PhSO.sub.3, PhSO.sub.3, p-CH.sub.3PhSO.sub.3 and the like.

(304) The general procedures for the compounds of the present invention are described as follows. Any starting materials are readily available ar are prepared by techniques and procedures readily available to one skilled in the art.

(305) For example, the compound of the present invention represented by formula (I) and (I) can be prepared by the following synthetic route.

(306) A Method for Preparing the Formula b5

(307) ##STR00076##
wherein R.sup.b1, R.sup.b2, R.sup.b3 and R.sup.b4 are each independently hydrogen, halogen, hydroxy, carboxy, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkenyloxy, substituted or unsubstituted alkynyloxy, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkenylsulfanyl, substituted or unsubstituted alkynylsulfanyl, substituted or unsubstituted amino, substituted or unsubstituted carbamoyl, substituted or unsubstituted sulfamoyl, substituted or unsubstituted alkylcarbonyl, substituted or unsubstituted alkenylcarbonyl, substituted or unsubstituted alkynylcarbonyl, substituted or unsubstituted alkyloxycarbonyl, substituted or unsubstituted alkenyloxycarbonyl substituted or unsubstituted alkynyloxycarbonyl or substituted or unsubstituted sulfamoyl; R.sup.b5 is substituted or unsubstituted alkyl.
Step 1 Preparation of the Compound b2

(308) The compound b2 can be obtained by reacting a solution of the compound b1 in the presence of iron.

(309) Examples of the reaction solvent include water, ethanol, methanol, THF, toluene and the like, and their mixed solvents can be used as well as the single solvent.

(310) Examples of the additive include ammonium chloride, hydrochloric acid and the like. The amount thereof may be 1 to 10 mole equivalent(s), preferably 1 to 3 mole equivalent(s), for 1 mole equivalent of the compound b1.

(311) The reaction temperature may be room temperature to heating under reflux, preferably room temperature to 100 C.

(312) The reaction time may be 1 to 48 hour(s), preferably 1 to 5 hour(s).

(313) Step 2 Preparation of the Compound b3

(314) The compound b3 can be obtained by reacting a solution of the compound b2 with a calboxylic acid in presence of a condensing agent.

(315) Examples of the reaction solvent include DMF, NMP, THF and the like, their mixed solvent can be used as well as the single solvent.

(316) Examples of the condensing agent include HATU, dicyclohexylcarbodiimide, carbonyl diimidazole, dicyclohexylcarbodiimido-N-hydroxy benzotriazole, EDC, 4-(4,6-dimethyloxy-1,3,5,-triazine-2-yl)-4-methyl morpholinium chloride and the like. The amount thereof may be 1 to 10 mole equivalent(s), preferably 1 to 3 mole equivalent(s), for 1 mole equivalent of the compound b2.

(317) The reaction temperature may be room temperature to heating under reflux, preferably room temperature to 50 C.

(318) The reaction time may be 1 to 48 hour(s), preferably 1 to 5 hour(s).

(319) Step 3 Preparation of the Compound b4

(320) The compound b4 can be obtained by reacting a solution of the compound b3 in presence of a base.

(321) Examples of the reaction solvent include NMP, DMF, THF and the like, their mixed solvent can be used as well as the single solvent.

(322) Examples of the base include cesium carbonate, potassium carbonate, sodium carbonate and the like. The amount thereof may be 1 to 10 mole equivalent(s), preferably 1 to 3 mole equivalent(s), for 1 mole equivalent of the compound b3.

(323) The reaction temperature may be room temperature to heating under reflux, preferably room temperature to 120 C.

(324) The reaction time may be 0.5 to 48 hour(s), preferably 1 to 5 hour(s).

(325) Step 4 Preparation of the Compound b5

(326) The compound b5 can be obtained by reacting a solution of the compound b4 in presence of a Lewis acid.

(327) Examples of the reaction solvent include toluene, methylene chloride, THF and the like, their mixed solvent can be used as well as the single solvent.

(328) Examples of the Lewis acid include aluminum chloride, include trifluoroborane-ether complex and the like. The amount thereof may be 1 to 10 mole equivalent(s), preferably 1 to 3 mole equivalent(s), for 1 mole equivalent of the compound b4.

(329) The reaction temperature may be room temperature to heating under reflux, preferably room temperature to 120 C.

(330) The reaction time may be 1 to 48 hour(s), preferably 1 to 5 hour(s).

(331) A Method for Preparing the Formula (Ia)

(332) ##STR00077##
wherein R.sup.2 is substituted or unsubstituted alkyl; R.sup.4 is substituted or unsubstituted alkylcarbonyl, substituted or unsubstituted alkenylcarbonyl, substituted or unsubstituted alkynylcarbonyl, substituted or unsubstituted non-aromatic carbocyclylcarbonyl, substituted or unsubstituted aromatic carbocyclylcarbonyl, substituted or unsubstituted non-aromatic heterocyclylcarbonyl, substituted or unsubstituted aromatic heterocyclylcarbonyl, substituted or unsubstituted alkyloxycarbonyl, substituted or unsubstituted alkenyloxycarbonyl, substituted or unsubstituted alkynyloxycarbonyl, substituted or unsubstituted non-aromatic carbocyclyloxycarbonyl, substituted or unsubstituted aromatic carbocyclyloxycarbonyl, substituted or unsubstituted non-aromatic heterocyclyloxycarbonyl, substituted or unsubstituted aromatic heterocyclyloxycarbonyl or substituted or unsubstituted carbamoyl; each R.sup.6 is independently hydrogen, halogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl or substituted or unsubstituted alkynyl; each R.sup.7 is independently hydrogen, halogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl or substituted or unsubstituted alkynyl, or R.sup.6 and R.sup.7 on the same carbon atom may be taken together to form a ring, or R.sup.2 may be taken together with either R.sup.6 or R.sup.7 to form a ring; each n is independently an integer of 1, 2 or 3; ring A is substituted or unsubstituted benzene, substituted or unsubstituted 4- to 6-membered non-aromatic carbocycle, substituted or unsubstituted 5- to 6-membered aromatic heterocycle or substituted or unsubstituted 4- to 6-membered non-aromatic heterocycle, Y.sup.1 is a leaving group; Pr is an protecting group of amino.
Step 1 Preparation of the Compound b7

(333) The compound b7 can be obtained by reacting a solution of the compound b6 with an alcohol in the presence of a phosphine reagent and a condensing agent.

(334) Examples of the reaction solvent include 1,4-dioxane, THF, diethylether and the like, their mixed solvent can be obtained as well as the single solvent.

(335) Examples of the condensing agent include dimethyl oxyethyl azodicarboxylate, diethyl azodicarboxylate and the like. The amount thereof may be 1 to 10 mole equivalent(s), preferably 1 to 3 mole equivalent(s), for 1 mole equivalent of the compound b7.

(336) Examples of the alcohol include a primary alcohol such as (S)-t-butyl-1-hydroxy propy-2-yl carbamate etc., a secondary alcohol and the like. The amount thereof may be 1 to 10 mole equivalent(s), preferably 1 to 3 mole equivalent(s), for 1 mole equivalent of the compound b7.

(337) Examples of the phosphine reagent include triphenylphosphine and the like. The amount thereof may be 1 to 1-mole equivalent(s), preferably 1 to 3 mole equivalent(s), for 1 mole equivalent of the compound b7.

(338) The reaction temperature may be 0 C. to heating under reflux, preferably 0 C. to room temperature.

(339) The reaction time may be 0.5 to 48 hour(s), preferably 1 to 5 hour(s).

(340) Step 2 Preparation of the Compound b8

(341) The compound b8 can be obtained by reacting with an acid anhydride in presence of a base after deprotecting the compound b7.

(342) Examples of the deprotecting agent include hydrochloric acid-1,4-dioxane, hydrochloride-ethyl acetate, hydrochloric acid-methanol, TFA, toluene sulfonic acid and the like. The amount thereof may be 1 mole equivalent excess quantity, preferably 1 to 10 mole equivalent(s), for 1 mole equivalent of the compound b7.

(343) Examples of the reaction solvent include 1,4-dioxane, methylene chloride, ethyl acetate, methanol and the like, their mixed solvent can be used as well as the single solvent.

(344) Examples of the acid anhydride include acetic acid anhydride, trifluoroacetic acid anhydride and the like. The amount thereof may be 1 to 10 mole equivalent(s), preferably 1 to 3 equivalent(s), for 1 mole equivalent of the compound b7.

(345) Examples of the base include pyridine, triethylamine, diisopropylethylamine and the like. The amount thereof may be 1 to 10 mole equivalent(s), preferably 1 to 3 mole equivalent(s), for 1 mole equivalent of the compound b7.

(346) The reaction temperature may be 0 C. to heating under reflux, preferably 0 C. to room temperature.

(347) The reaction time may be 0.1 to 48 hour(s), preferably 1 to 5 hour(s).

(348) Step 3 Preparation of the Compound (Ia)

(349) The compound (Ia) can be obtained by reacting a solution of the compound b8 with an alcohol in presence of a ligand, a base and a metal catalyst.

(350) Examples of the ligand include N,N-dimethylglycine, glycine, methylglycine and the like. The amount thereof may be 1 to 10 mole equivalent(s), preferably 1 to 3 mole equivalent(s), for 1 mole equivalent of the compound b8.

(351) Examples of the reaction solvent may be 1,4-dioxane, THF, DMF and the like, their mixed solvent can be used as well as the single solvent.

(352) Examples of the metal catalyst include copper iodide, copper chloride, copper bromide and the like. The amount thereof may be 0.001 to 2 mole equivalent(s), preferably 0.01 to 0.5 mole equivalent(s), for 1 mole equivalent of the compound b8.

(353) Examples of the base include cesium carbonate, potassium carbonate, sodium carbonate and the like. The amount thereof may be 1 to 10 mole equivalent(s), preferably 1 to 3 mole equivalent(s), for 1 mole equivalent of the compound b8.

(354) The reaction temperature may be room temperature to heating under reflux, preferably 50 C. to heating under reflux.

(355) The reaction time may be 1 to 48 hour(s), preferably 1 to 5 hour(s).

(356) A Method for Preparing the Compound b12

(357) ##STR00078##
wherein each R.sup.b6 and R.sup.b7 is independently hydrogen, halogen, hydroxy, carboxy, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkenyloxy, substituted or unsubstituted alkynyloxy, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkenylsulfanyl, substituted or unsubstituted alkynylsulfanyl, substituted or unsubstituted amino, substituted or unsubstituted carbamoyl, substituted or unsubstituted sulfamoyl, substituted or unsubstituted alkylcarbonyl, substituted or unsubstituted alkenylcarbonyl, substituted or unsubstituted alkynylcarbonyl, substituted or unsubstituted alkyloxycarbonyl, substituted or unsubstituted alkenyloxycarbonyl, substituted or unsubstituted alkynyloxycarbonyl or substituted or unsubstituted sulfamoyl; R.sup.b8 is substituted or unsubstituted alkyl; Y.sup.1 is a leaving group; Y.sup.2 is halogen; Y.sup.3 is halogen.
Step 1 Preparation of the Compound b10

(358) The compound b10 can be obtained by reacting an alcohol solution of the compound b9 in presence of a base.

(359) Examples of the alcohol include methanol, ethanol, isopropanol and the like.

(360) Examples of the base include sodium hydride, potassium hydride, sodium hydroxide, potassium hydroxide, potassium carbonate, cesium carbonate and the like. The amount thereof may be 1 to 5 mole equivalent(s), preferably 1 to 3 mole equivalent(s), for 1 mole equivalent of the compound b9.

(361) The reaction temperature may be 0 C. to heating under reflux, preferably room temperature to 100 C.

(362) The reaction time may be 0.1 to 24 hour(s), preferably 0.1 to 3 hour(s).

(363) Step 2 Preparation of the Compound b11

(364) The compound b11 can be obtained by reacting a solution of the compound b10 with a borane reagent in presence of, a base and a palladium catalyst then oxidizing them.

(365) Examples of the borane reagent include 4,4,4,4,5,5,5,5-octamethyl-2,2-bis(1,3,2-dioxaborane), triethylborane, trimethyl borane and the like. The amount thereof may be 1 to 10 mole equivalent(s), preferably 1 to 3 mole equivalent(s), for 1 mole equivalent of the compound b10.

(366) Examples of the reaction solvent include methylene chloride, 1,4-dioxane, THF and the like, their mixed solvent can be used as well as the single solvent.

(367) Examples of the base include sodium acetate, potassium acetate, sodium carbonate, potassium carbonate and the like. The amount thereof may be 1 to 10 mole equivalent(s), preferably 1 to 3 mole equivalent(s), for 1 mole equivalent of the compound b10.

(368) Examples of the palladium catalyst include chloride (diphenylphosphino ferrocene) palladium dichloromethane complex, palladium acetate, bis(dibenzylideneacetone)palladium, tetrakis(triphenylphosphine)palladium, bis(triphenylphosphine)palladium(II)dichloride, bis(tri-tert-butylphosphine)palladium and the like. The amount thereof may be 0.001 to 1 mole equivalent, preferably 0.01 to 0.5 mole equivalents, for 1 mole equivalent of the compound b10.

(369) Examples of the oxidant include hydrogen peroxide, m-chloroperbenzoic acid and the like. The amount thereof may be 1 to 10 mole equivalent(s), preferably 5 to 10 mole equivalent(s), for 1 mole equivalent of the compound b10.

(370) The reaction temperature may be 0 C. to heating under reflux, preferably room temperature to 130 C.

(371) The reaction time may be 0.1 to 48 hour(s), preferably 0.5 to 5 hour(s).

(372) Step 3 Preparation of the Compound b12

(373) The compound b12 can be obtained by reacting a solution of the compound b11 in presence of a metal catalyst and a halogenating agent.

(374) Examples of the reaction solvent include DMF, NMP, THF and the like, their mixed solvent can be used as well as the single solvent.

(375) Examples of the metal catalyst include zirconium chloride, bis(cyclopentadienyl)zirconium chloride hydride and the like. The amount thereof may be 0.01 to 1 mole equivalent, preferably 0.1 to 0.5 mole equivalents, for 1 mole equivalent of the compound b11.

(376) Examples of the halogenating agent include N-chlorosuccinimide, N-bromosuccinimide and the like. The amount thereof may be 1 to 10 mole equivalent(s), preferably 1 to 3 mole equivalent(s), for 1 mole equivalent of the compound b11.

(377) The reaction temperature may be 0 C. to heating under reflux, preferably room temperature to 100 C.

(378) The reaction time may be 0.5 to 48 hour(s), preferably 0.5 to 5 hour(s).

(379) Preparation of the Compound b15

(380) ##STR00079##
wherein each R.sup.b9 and R.sup.b10 is independently hydrogen, halogen, hydroxy, carboxy, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkenyloxy, substituted or unsubstituted alkynyloxy, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkenylsulfanyl, substituted or unsubstituted alkynylsulfanyl, substituted or unsubstituted amino, substituted or unsubstituted carbamoyl, substituted or unsubstituted sulfamoyl, substituted or unsubstituted alkylcarbonyl, substituted or unsubstituted alkenylcarbonyl, substituted or unsubstituted alkynylcarbonyl, substituted or unsubstituted alkyloxycarbonyl, substituted or unsubstituted alkenyloxycarbonyl, substituted or unsubstituted alkynyloxycarbonyl or substituted or unsubstituted sulfamoyl; R.sup.b11 is substituted or unsubstituted alkyl; R.sup.b12 is substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl or substituted or unsubstituted alkynyl.
Step 1 Preparation of the Compound b14

(381) The compound b14 can be obtained by reacting a solution of the compound b13 with an acid chloride in presence of a base.

(382) Examples of the base include pyridine, tirethylamine, diisopropylethylamine, potassium carbonate ad the like, it is also possible to use as a solvent.

(383) Examples of the acid chloride include chloride isobutyl acid, acetyl chloride, trifluoroacetyl chloride and the like. The amount thereof can be 1 to 10 mole equivalent(s), preferably 1 to 3 mole equivalent(s), for 1 mole equivalent of the compound b13.

(384) The reaction temperature may be 0 C. to heating under reflux, preferably 0 C. to 50 C.

(385) The reaction time may be 0.1 to 48 hour(s), preferably 0.1 to 3 hour(s).

(386) Step 2 Preparation of the Compound b15

(387) The compound b15 can be obtained by reacting a solution of the compound b14 with Lawesson's reagent, with a base, then with a Lewis acid.

(388) Examples of the solvent include toluene, methylene chloride and the like, their mixed solvent can be used as well as the single solvent.

(389) The amount of Lawesson's reagent may be 0.5 to 10 mole equivalent(s), preferably 0.5 to 3 mole equivalent(s), for 1 mole equivalent of the compound b14.

(390) The reaction temperature may be room temperature to heating under reflux, preferably room temperature to 120 C.

(391) The reaction time may be 0.5 to 48 hour(s), preferably 1 to 5 hour(s).

(392) Examples of the base include cesium carbonate, potassium carbonate, sodium carbonate and the like. The amount thereof can be 1 to 10 mole equivalent(s), preferably 1 to 3 mole equivalent(s) for 1 mole equivalent of the compound b14.

(393) Examples of the solvent include DMF, NMP and the like, their mixed solvent can be used as well as the single solvent.

(394) The reaction temperature may be room temperature to heating under reflux, preferably room temperature to 120 C.

(395) The reaction time may be 1 to 48 hour(s), preferably 1 to 5 hour(s).

(396) Examples of the Lewis acid include tribromoborane, trichloroborane, aluminum chloride. The amount thereof can be 1 to 10 mole equivalent(s), preferably 1 to 5 mole equivalent(s).

(397) Preparing of the Compound b19

(398) ##STR00080##
wherein R.sup.2 is substituted or unsubstituted alkyl; R.sup.4 is substituted or unsubstituted alkylcarbonyl, substituted or unsubstituted alkenylcarbonyl, substituted or unsubstituted alkynylcarbonyl, substituted or unsubstituted non-aromatic carbocyclylcarbonyl, substituted or unsubstituted aromatic carbocyclylcarbonyl, substituted or unsubstituted non-aromatic heterocyclylcarbonyl, substituted or unsubstituted aromatic heterocyclylcarbonyl, substituted or unsubstituted alkyloxycarbonyl, substituted or unsubstituted alkenyloxycarbonyl, substituted or unsubstituted alkynyloxycarbonyl, substituted or unsubstituted non-aromatic carbocyclyloxycarbonyl, substituted or unsubstituted aromatic carbocyclyloxycarbonyl, substituted or unsubstituted non-aromatic heterocyclyloxycarbonyl, substituted or unsubstituted aromatic heterocyclyloxycarbonyl or substituted or unsubstituted carbamoyl; each R.sup.6 is independently hydrogen, halogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl or substituted or unsubstituted alkynyl; each R.sup.7 is independently hydrogen, halogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl or substituted or unsubstituted alkynyl, or R.sup.6 and R.sup.7 bonded to the same carbon atom may be taken together to form a ring, or R.sup.2 may be taken together with either R.sup.6 or R.sup.7 to form a ring; each n is independently an integer of 1, 2 or 3; ring A substituted or unsubstituted benzene, substituted or unsubstituted 4- to 6-membered non-aromatic carbocycle, substituted or unsubstituted 5- to 6-membered aromatic heterocycle or substituted or unsubstituted 4- to 6-membered non-aromatic heterocycle, Y.sup.1 is a leaving group; Pr is a protecting group of amino.
Step 1 Preparation of the Compound b18

(399) The compound b18 can be obtained by reacting a solution of the compound b17 with oxathiazolidine dioxide in presence of a base.

(400) Examples of the solvent include DMF, NMP, THF, methylene chloride and the like, their mixed solvent can be obtained as well as the single solvent.

(401) Examples of the base include sodium hydride, potassium hydride and the like. The amount thereof may be 1 to 10 mole equivalent(s), preferably 1 to 3 mole equivalent(s), for 1 mole equivalent of the compound b17.

(402) Examples of oxathiazolidine dioxide include (S)-3-benzyl-4-methyl-1,2,3-oxathiazolidine-2,2-dioxide and the like. The amount thereof may be 1 to 10 mole equivalent(s), preferably 1 to 3 mole equivalent(s), for 1 mole equivalent of the compound b17.

(403) The reaction temperature may be 0 C. to heating under reflux, preferably 0 C. to 50 C.

(404) The reaction time may be 0.1 to 48 hour(s), preferably 0.1 to 3 hour(s).

(405) Step 2 Preparation of the Compound b19

(406) The compound b19 can be obtained by reacting with a deprotecting agent, after reacting a solution of the compound b18 with an acid anhydrate in presence of a additive and a palladium catalyst.

(407) Examples of the solvent include methanol, ethanol, THF, ethyl acetate, water and the like, their mixed solvent can be used as well as the single solvent.

(408) Examples of the metallic catalyst include palladium hydroxide, palladium chloride, palladium on carbon, platinum oxide and the like. The amount thereof may be 0.001 to 1 mole equivalent, preferably 0.01 to 0.5 mole equivalents, for 1 mole equivalent of the compound b18.

(409) Examples of the additive include ammonium formate, triethylamine formic acid and the like. The amount thereof can be 1 to 10 mole equivalent(s), preferably 1 to 3 mole equivalent(s), for 1 mole equivalent of the compound b17.

(410) The reaction temperature may be 0 C. to heating under reflux, preferably room temperature to 80 C.

(411) The reaction time may be 0.1 to 48 hour(s), preferably 1 to 5 hour(s).

(412) Examples of the acid anhydride include acetic anhydride, include trifluoroacetic anhydride and the like. The amount thereof may be 1 to 10 mole equivalent(s), preferably 1 to 3 mole equivalent(s) for 1 mole equivalent of the compound b18.

(413) Examples of the base include pyridine, triethylamine diisopropylethylamine and the like. The amount thereof can be 1 to 10 mole equivalent(s), preferably 1 to 3 mole equivalent(s) for 1 mole equivalent of the compound b18.

(414) The reaction temperature may be 0 C. to heating under reflux, preferably 0 C. to 100 C.

(415) The reaction time may be 0.1 to 48 hour(s), preferably 1 to 24 hour(s).

(416) Examples of the deprotecting agent include tetrabutylammonium fluoride, hydrogen fluoride, hydrogen fluoride-pyridine and the like. The amount thereof may be 1 to 10 mole equivalent(s), preferably 1 to 3 mole equivalent(s) for 1 mole equivalent of the compound b18.

(417) The reaction temperature may be 0 C. to heating under reflux, preferably 0 C. to 100 C.

(418) The reaction time may be 0.1 to 48 hour(s), preferably 1 to 24 hour(s).

(419) Preparing of the Compound b26

(420) ##STR00081##
wherein R.sup.b13, R.sup.b14, R.sup.b15 and R.sup.b16 are each independently hydrogen, halogen, hydroxy, carboxy, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkenyloxy, substituted or unsubstituted alkynyloxy, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkenylsulfanyl, substituted or unsubstituted alkynylsulfanyl, substituted or unsubstituted amino, substituted or unsubstituted carbamoyl, substituted or unsubstituted sulfamoyl, substituted or unsubstituted alkylcarbonyl, substituted or unsubstituted alkenylcarbonyl, substituted or unsubstituted alkynylcarbonyl, substituted or unsubstituted alkyloxycarbonyl, substituted or unsubstituted alkenyloxycarbonyl, substituted or unsubstituted alkynyloxycarbonyl or substituted or unsubstituted sulfamoyl; R.sup.b17 is substituted or unsubstituted alkyl; R.sup.b18 is substituted or unsubstituted alkyl; ring A is substituted or unsubstituted benzene, substituted or unsubstituted 4- to 6-membered non-aromatic carbocycle, substituted or unsubstituted 5- to 6-membered aromatic heterocycle or substituted or unsubstituted 4- to 6-membered non-aromatic heterocycle.
Step 1 Preparation of the Compound b24

(421) The compound b24 can be obtained by reacting a solution of the compound b23 with a halide in presence of a base.

(422) Examples of the solvent include DMF, NMP, THF and the like, their mixed solvent can be used as well as the single solvent.

(423) Examples of the base include potassium carbonate, sodium carbonate, cesium carbonate and the like. The amount thereof may be 1 to 10 mole equivalent(s), preferably 1 to 3 mole equivalent(s), for 1 mole equivalent of the compound b23.

(424) The reaction temperature may be 0 C. to heating under reflux, preferably room temperature to heating under reflux.

(425) The reaction time may be 1 to 24 hour(s), preferably 1 to 5 hour(s).

(426) Step 2 Preparation of the Compound b25

(427) The compound b25 can be obtained by reacting a solution of the compound b24 with a Lewis acid.

(428) Examples of the solvent include methylene chloride and the like, their mixed solvent can be used as well as the single solvent.

(429) Examples of the Lewis acid include aluminum chloride, include trifluoroborane-ether complex and the like. The amount thereof may be 1 to 10 mole equivalent(s), preferably 1 to 3 mole equivalent(s), for 1 mole equivalent of the compound b24.

(430) The reaction temperature may be 78 C. to 50 C., preferable 78 C. to room temperature.

(431) The reaction time may be 1 to 24 hour(s), preferably 1 to 5 hour(s).

(432) Step 3 Preparation of the Compound b26

(433) The compound b26 can be obtained by reacting a solution of the compound b25 with a halide in presence of a base.

(434) Examples of the solvent include DMF, NMP, THF and the like, their mixed solvent can be used as well as the single solvent.

(435) Examples of the base include potassium carbonate, sodium carbonate, cesium carbonate and the like. The amount thereof can be 1 to 10 mole equivalent(s), preferably 1 to 3 mole equivalent(s), for 1 mole equivalent of the compound b25.

(436) Examples of the halide include alkyl bromide, alkyl chlorides and the like. The amount thereof can be 1 to 10 mole equivalent(s), preferably 1 to 3 mole equivalent(s), for 1 mole equivalent of the compound b25.

(437) The reaction temperature may be 0 C. to heating under reflux, preferable room temperature to 100 C.

(438) The reaction time may be 1 to 24 hour(s), preferably 1 to 5 hour(s).

(439) Preparing of the Compound b29

(440) ##STR00082##
wherein R.sup.2 is substituted or unsubstituted alkyl; R.sup.b20, R.sup.b21, R.sup.b22, R.sup.b23 and R.sup.b24 are each independently hydrogen, halogen, hydroxy, carboxy, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkenyloxy, substituted or unsubstituted alkynyloxy, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkenylsulfanyl, substituted or unsubstituted alkynylsulfanyl, substituted or unsubstituted amino, substituted or unsubstituted carbamoyl, substituted or unsubstituted sulfamoyl, substituted or unsubstituted alkylcarbonyl, substituted or unsubstituted alkenylcarbonyl, substituted or unsubstituted alkynylcarbonyl, substituted or unsubstituted alkyloxycarbonyl, substituted or unsubstituted alkenyloxycarbonyl, substituted or unsubstituted alkynyloxycarbonyl or substituted or unsubstituted sulfamoyl; -L.sup.1- is O(CR.sup.6R.sup.7)m-; each R.sup.6 is independently hydrogen, halogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl or substituted or unsubstituted alkynyl; each R.sup.7 is independently hydrogen, halogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl or substituted or unsubstituted alkynyl; or R.sup.6 and R.sup.7 bonded to the same carbon atom may be taken together to form a ring, or R.sup.2 may be taken together with either R.sup.6 or R.sup.7 to form a ring; each m is independently an integer of 0, 1, 2 or 3; ring A is substituted or unsubstituted benzene, substituted or unsubstituted 4- to 6-membered non-aromatic carbocycle, substituted or unsubstituted 5- to 6-membered aromatic heterocycle or substituted or unsubstituted 4- to 6-membered non-aromatic heterocycle; Pr is a protecting group of amino.
Step 1 Preparation of the Compound b29

(441) The compound b26 can be obtained by reacting a solution of the compound b26 with Weinreb amides in presence of a base.

(442) Examples of the solvent include THF, diethylether and the like, their mixed solvent can be used as well as the single solvent.

(443) Examples of the base include n-butyllithium, sec-butyl lithium, t-butyl lithium, lithium hexamethyl distill amide and the like. The amount thereof may be 1 to 10 mole equivalent(s), preferably 1 to 3 mole equivalent(s), for 1 mole equivalent of the compound b25.

(444) The amount of the Weinreb amide may be 1 to 10 mole equivalent(s), preferably 1 to 3 mole equivalent(s), for 1 mole equivalent of the compound b26.

(445) The reaction temperature may be 78 C. to 50 C., preferably 78 C. to room temperature.

(446) The reaction time may be 0.1 to 24 hour(s), preferably 0.5 to 5 hour(s).

(447) The compound of the present invention has ACC2 inhibitory activity. Moreover, the compound of the present invention can be a medicine which is reduced the side effect, because of having high ACC2 selectivity as against ACC1. Additionally, the compound of the present invention can be a medicine which is rescued the side effect, because of low cardiovascular or MBI risks. A pharmaceutical composition comprising the compound of the present invention is very useful for preventing or treating a disease associated with ACC2. Examples of the diseases associated with ACC2 means a disease induced by malonyl-CoA produced by ACC2 are metabolic syndrome, obesity, diabetes, insulin resistance, abnormal glucose tolerance, diabetic peripheral neutopathy, diabetic nephropathy, diabetic retinal disease, diabetic macroangiopathy, hyperlipidemia, hypertension, cardiovascular illness, arterioscerosis, atherosclerosis, cardiac arrest, cardiac infarction, infectious disease, neoplasm and the like. A pharmaceutical composition comprising the compound of the present invention is very useful as a medicine for preventing or treating these disease.

(448) A compound of the present invention has not only ACC2 inhibitory activity but also usefulness as a medicine and any or all good characters selected from the followings: a) weak CYP enzyme (e.g., CYP1A2, CYP2C9, CYP2C19, CYP2D6, CYP3A4 etc.) inhibition. b) good drug disposition such as high bioavailavility, appropriate clearance and the like. c) high metabolic stability. d) no irreversible CYP enzyme (e.g., CYP3A4) inhibition in the range of the concentration as a measuring condition described in the specification. e) no mutagenicity. f) low cardiovascular risk. g) high water solubility.

(449) The pharmaceutical composition of the invention can be administered orally or parenterally as an anti-obesity agent or anorectic agent. In the case of oral administration, it may be in any usual form such as tablets, granules, powders, capsules and the like. When the compound is parenterally administered, any usual form is preferable injections and the like. Oral administration is especially preferable because the compounds of the present invention show a high oral absorbability.

(450) The pharmaceutical composition may be manufactured by mixing an effective amount of the compound of the present invention with various pharmaceutical additives suitable for the administration form, such as excipients, binders, moistening agents, disintegrants, lubricants and the like.

(451) Although the dosage of the pharmaceutical composition of the invention as an anti-obesity agent or anorectic agent should be determined in consideration of the patient's age and body weight, the type and degree of diseases, the administration route and the like, a usual oral dosage for an adult is 0.05 to 100 mg/kg/day, preferable is 0.1 to 10 mg/kg/day. For parenteral administration, although the dosage highly varies with administration routes, a usual dosage is 0.005 to 10 mg/kg/day, preferably 0.01 to 1 mg/kg/day. The dosage may be administered in one to several divisions per day.

EXAMPLES

(452) The present invention is further explained by the following Examples and references, which are not intended to limit the scope of this invention.

(453) The abbreviations used in the present description stand for the following meanings. Ac: acetyl Bu: butyl dba: dibenzylideneacetone DMF: N,N-dimethylformamide Et: ethyl HATU: O-(7-azabenzotriazole-1-yl)-1,1,3,3-tetramethyl uranium hexafluorophosphate Me: methyl NMP: N-methyl-2-pyrrolidone Pd.sub.2(dba).sub.3: tris(dibenzylideneacetone)bispalladium Ph: phenyl Tf: trifluoromethanesulfonyl THF: tetrahydrofuran

(454) .sup.1H NMR spectra of the examples were measured on 300 MHz in d.sub.6-DMSO or CDCl.sub.3.

(455) RT in the examples or the tables represents Retention Time by LC/MS: Liquid Chromatography/Mass Spectrometry. LC/MS data of the compounds were measured under the following condition. Method 1: Column: Gemini-NX (5 m, i.d. 4.650 mm (Phenomenex) Flow rate: 3.0 mL/min UV detection wavelength: 254 nm

(456) Mobile phase: [A] is 0.1% formic acid-containing aqueous solution, [B] is 0.1% formic acid-containing acetonitrile solution Gradient: Linear gradient of 5% to 100% solvent [B] for 3.5 minutes was performed, and 100% solvent [B] was maintained for 0.5 minutes. Method 2: Column: Shim-pack XR-ODS (2.2 m, i.d. 503.0 mm (Shimadzu) Flow late: 1.6 mL/min UV detection wavelength: 254 nm Mobile phase: [A] is 0.1% formic acid-containing aqueous solution, [B] is 0.1% formic acid-containing acetonitrile solution Gradient: Linear gradient of 10% to 100% solvent [B] for 3 minutes was performed, and 100% solvent [B] was maintained for 1 minute. Method 3: Column: ACQUITY UPLC(R) BEH C18 (1.7 m, i.d. 2.150 mm (Waters) Flow rate: 0.55 mL/min UV detection wavelength: 254 nm Mobile phase: [A] is 0.1% formic acid-containing aqueous solution, and [B] is 0.1% formic acid-containing acetonitrile solution Gradient: Linear gradient of 5% to 100% solvent [B] for 3 minutes was performed, and 100% solvent [B] was maintained for 0.5 minutes. Method 4: Column: ACQUITY UPLC(R)BEH C18 (1.7 m i.d. 2.150 mm (Waters) Flow rate: 0.8 mL/min UV detection wavelength: 254 nm Mobile phase: [A] is 0.1% formic acid-containing aqueous solution, and [B] is 0.1% formic acid-containing acetonitrile solution Gradient: Linear gradient of 5% to 100% solvent [B] for 3.5 minutes was performed, and 100% solvent [B] was maintained for 0.5 minutes. Method 5: Column: Shim-pack XR-ODS (2.2 m, i.d. 503.0 mm (Shimadzu) Flow rate: 1.6 mL/min UV detection wavelength: 254 nm Mobile phase: [A] is 0.1% formic acid-containing aqueous solution, and [B] is 0.1% formic acid-containing acetonitrile solution Gradient: Linear gradient of 10% to 100% solvent [B] for 8 minutes was performed, and 100% solvent [B] was maintained for 0.5 minutes.

Example 1

Preparation of Compound a2

(457) ##STR00083##
Step 1 Preparation of Compound a2

(458) Compound a1 (3.0 g, 16 mmol) was dissolved in ethanol (30 mL) and water (10 mL), and iron (2.7 g, 48 mmol) and ammonium chloride (2.6 g, 48 mmol) were added into the reaction mixture, the reaction mixture was stirred at 80 C. for 4 hours. The mixtures are filtered, and water was added into the mother liquor. The reaction mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over magnesium sulfate. The organic layer was condensed under reduced pressure to afford Compound a2 (2.5 g) as crude.

(459) M+H=159.6, Method Condition 4: retention time 1.07 min

(460) Step 2 Preparation of Compound a3

(461) Compound a2 (2.5 g, 16 mmol) was dissolved in DMF (30 mL), and isobutyric acid (1.7 g, 19 mmol) and O-(7-Azabenzotriazol-1-yl)-1,1,3,-tetramethyluronium hexafluorophosphate (7.8 g, 21 mmol) and triethyl amine (3.1 g, 32 mmol) was added to the reaction mixture while cooling in ice. The reaction mixture was stirred at room temperature overnight. Water was added into the mixture and the mixture was extracted with diethyl ether. The organic layer was washed with saturated brine, and dried over magnesium sulfate. The solvent was condensed under reduced pressure to afford Compound a3 (5.1 g) as crude.

(462) M+H=229.8, Method Condition 4: retention time 1.54 min

(463) Step 3 Preparation of Compound a4

(464) Compound a3 (2.0 g, 8.7 mmol) was dissolved in NMP (1.0 mL), and cesium carbonate (5.7 g, 17 mmol) was added to the mixture. The mixture was stirred at 160 C. for 12 hours. DMF (13 mL) was added to the mixture, and the mixture was stirred at 100 C. for 1 hour. Water was added to the mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with hydrochloric acid and saturated brine, and dried over magnesium sulfate. The solvent was condensed under reduced pressure. The residue was purified by silica gel chromatography (hexane-ethyl acetate) to afford Compound a4 (0.46 g, yield 25%).

(465) .sup.1H NMR (CDCl3) : 1.46 (d, J=7.0 Hz, 6H), 3.31-3.17 (m, 1H), 3.95 (s, 3H), 6.97 (dd, J=8.0, 4.0 Hz, 1H), 7.36 (d, J=8.8 Hz, 1H).

(466) M+H=209.8, Method Condition 4: retention time 2.04 min

(467) Step 4 Preparation of Compound a5

(468) Compound a4 (0.36 g, 1.7 mmol) was dissolved in toluene (8.0 mL), and aluminum chloride (0.57 g, 4.3 mmol) was added to the mixture. The mixture was stirred at 100 C. for 2 hours. The sodium acetate solution was added to the mixture while cooling in ice, and the mixture was extracted with diethyl ether. The organic layer was washed with saturated brine, and dried over magnesium sulfate. The solvent was condensed under reduced pressure. The solid was filtrated to afford Compound a5 (0.28 g, yield 83%).

(469) .sup.1H NMR (CDCl3) : 1.46 (d, J=6.9 Hz, 6H), 3.21-3.28 (m, 1H), 5.54 (s, 1H), 6.98 (dd, J=8.1 Hz, 1H), 7.32 (d, J=8.5 Hz, 1H).

(470) [M+H]=195.7, Method Condition 2: retention time 1.55 min

Example 2

Preparation of Compound I-031

(471) ##STR00084##
Step 1 Preparation of Compound a7

(472) Compound a6 (1.0 g, 5.7 mmol) was dissolved in 1,4-dioxane (10 mL), and (s)-t-butyl-1-hydroxypurop-2-yl carbamate (1.2 g, 6.9 mmol), triphenylphosphine (1.8 g, 6.9 mmol) and dimethyloxyethylazodicarboxylate (1.6 g, 6.9 mmol) was added to the mixture while cooling in ice. The mixture was stirred at room temperature for I hour. Water was added to the mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over magnesium sulfate. The solvent was condensed under reduced pressure. The residue was purified by silica gel chromatography (hexane-ethyl acetate) to afford Compound a7 (1.3 g, yield 67%).

(473) [M+H]=332.0, Method Condition 4: retention time 2.16 min

(474) Step 2 Preparation of Compound a8

(475) Compound a7 (0.70 g, 2.1 mmol) was added to 4 mol/L hydrochloric acid-1,4-dioxane (5.3 mL), and the mixture was stirred at room temperature for 1 hour. The reaction solution was distilled off under reduced pressure, and the obtained residue was dissolved in methylene chloride (6.0 mL), pyridine (0.83 g, 11 mmol) and acetic anhydride (3.2 mg, 3.2 mmol) were added, and the mixture was stirred at room temperature for 1 hour. A saturated aqueous sodium hydrogen carbonate solution was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the precipitated solid was collected by filtration to give Compound a8 (0.54 g, 93% yield).

(476) .sup.1H NMR (CDCl.sub.3) : 1.28 (d, J=6.8 Hz, 3H), 1.99 (s, 3H), 4.29 (d, J=4.4 Hz, 2H), 4.38-4 51 (m, 1H), 5.58-5.73 (m, 1H), 8.05 (s, 1H), 8.18 (s, 1H).

(477) [M+H]=274.0, Method Condition 4: retention time 1.18 minutes

(478) Step 3 Preparation of Compound I-031

(479) Compounds a8 (30 mg, 0.11 mmol) was dissolved in 1,4-dioxane (1.0 mL) then, Compound a5 (47 mg, 0.22 mmol), copper iodide (6.3 mg, 0.033 mmol), N,N-dimethyl glycine (10 mg, 0.098 mmol) and cesium carbonate (0.11 g, 0.33 mmol) were added and the mixture was stirred at 130 C. under microwave irradiation for 4 hours. Water was added and the mixture was extracted with chloroform. The solvent was distilled off under reduced pressure, and the obtained residue was purified by silica gel column chromatography (chloroform-methanol) to give Compound I-031 (27 mg, 64% yield).

(480) .sup.1H NMR (CDCl.sub.3) : 1.29 (d, J=6.7 Hz, 3H), 1.48 (d, J=6.9 Hz, 6H), 1.99 (s, 3H), 3.21-3.36 (m, 1H), 4.29 (d, J=4.0 Hz, 2H), 4.36-4.49 (m, 1H), 5.67-5.81 (m, 1H), 7.15 (dd, J=7.7 Hz, 1H), 7.46 (d, J=8.5 Hz, 1H), 7.76 (s, 1H), 8.03 (s, 1H).

(481) [M+H]=389.2, Method Condition 4: retention time 1.97 minutes

Example 3

Preparation of Compound I-039

(482) ##STR00085##
Step 1 Preparation of Compound a10

(483) Compound a9 (20 g, 82 mmol) was dissolved in ethanol (0.16 L) and, 2 mol/L aqueous sodium hydroxide solution (45 mL, and 90 mmol) was added, and the mixture was stirred at 100 C. for 30 minutes. Water was added to the mixture, the precipitate was filtered and the filtrate was extracted with ethyl acetate. The organic layer was washed with saturated brine and dried with anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure to give Compound a10 (20 g, 95% yield).

(484) [M+H]=257.9, Method Condition 4: retention time 2.59 minutes

(485) Step 2 Preparation of Compound a11

(486) Compound a11 (20 g, 82 mmol) was dissolved in 1,4-dioxane (0.15 L) and 4,4,4,4,5,5,5,5-octamethyl-2,2-bis (1,3,2-dioxaborolan) (18 g, 70 mmol), sodium acetate (17 g, 0.17 mol) and chloride (diphenylphosphino ferrocene) palladium dichloromethane complex (4.8 g, 5.8 mmol) were added and the mixture was stirred at 110 C. for 2 hours. Water was added to the mixture, the precipitate was filtered and the filtrate was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The obtained residue was dissolved in dichloromethane (0.15 L), 30% aqueous hydrogen peroxide (59 mL, 0.58 mol) was added under ice-cooling, and the mixture was stirred at room temperature for 1 hour. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give compound a11 (13 g, 87% yield).

(487) [M+H]=196.1, Method Condition 4: retention time 1.54 minutes

(488) Step 3 Preparation of Compound a12

(489) Compound a11 (9.5 g, 49 mmol) was dissolved in DMF (0.20 L), zirconium chloride (2.3 g, 9.7 mmol) and N-chlorosuccinimide (6.8 g, 51 mmol) was added and the mixture was stirred at 50 C. for 1 hour. Hydrochloric acid aqueous solution was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give Compound a12 (8.4 g, 62% yield).

(490) .sup.1H NMR (CDCl.sub.3) : 1.47 (t, J=8.0 Hz, 3H), 4.58 (q, J=8.0 Hz, 2H), 5.44 (s, 1H), 7.04 (d, J=8.8 Hz, 1H), 7.47 (d, J=8.8 Hz, 1H).

(491) [M+H]=230.0, Method Condition 4: retention time 1.96 minutes

(492) Step 4 Preparation of Compound I-039

(493) Compound a8 (3.1 g, 10 mmol) was dissolved in 1,4-dioxane (40 mL), Compound a12 (2.0 g, 8.7 mmol), copper iodide (0.83 g, 4.4 mmol), N,N-dimethyl glycine (0.81 g, 7.8 mmol) and cesium carbonate (8.5 g, 26 mmol) were added and the mixture was stirred for 2 hours at 130 C. under microwave irradiation. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The solvent was distilled off under reduced pressure, and the obtained residue was purified by silica gel column chromatography (chloroform-ethyl acetate) to afford Compound I-039 (3.6 g, 64% yield).

(494) .sup.1H NMR (CDCl.sub.3) : 1.28 (d, J=6.8 Hz, 3H), 1.49 (t, J=7.2 Hz, 3H), 1.98 (s, 3H), 4.28 (d, J=4.0 Hz, 1H), 4.37-4.46 (m, 1H), 4.62 (q, J=7.2 Hz, 2H), 5.72 (bd, J=7.2 Hz, 1H), 7.18 (d, J=8.4 Hz, 1H), 7.58 (d, J=8.4 Hz, 1H), 7.77 (d, J=1.6 Hz, 1H), 7.98 (d, J=1.6 Hz, 1H).

(495) [M+H]=423.2, Method Condition 4: retention time 2.30 minutes

Example 4

Preparation of Compound I-038

(496) ##STR00086##
Step 1 Preparation of Compound a14

(497) Compound a13 (3.3 g, 23 mmol) was dissolved in pyridine (16 mL), isobutyric acid chloride (3.0 g, 28 mmol) was added and the mixture was stirred at room temperature for 30 minutes. Water was added to the reaction mixture and the mixture was extracted with ethyl acetate. The organic layer was washed with hydrochloric acid and saturated brine, and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and then filtered and the obtained solid was filtrated to afford Compound a14 (4.1 g, 83% yield).

(498) .sup.1H NMR (CDCl.sub.3) : 1.27 (d, J=8.0 Hz, 6H), 2.54 (m, 1H), 3.78 (s, 3H), 6.60-6.70 (m, 2H), 7.17 (bs, 1H), 8.10-8.20 (m, 1H).

(499) [M+H]=212.5, Method Condition 2: retention time 1.45 minutes

(500) Step 2 Preparation of Compound a15

(501) Compound a14 (1.7 g, 23 mmol) was dissolved in toluene (18 mL), Lawesson's reagent (1.9 g, 4.7 mmol) was added and the mixture was stirred at 110 C. for 2 hours. DMF (9.0 mL) and cesium carbonate (6.4 g, 20 mmol) was added to the reaction solution and the mixture was stirred at 100 C. for 2 hours. Water was added to the reaction mixture and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine and sodium bicarbonate solution, and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the obtained residue was dissolved in methylene chloride (25 mL), 1 mol/L tribromoborane dichloromethane solution (69 mL, 69 mmol) was added under ice cooling, and the mixture was stirred at room temperature for 1 hour. Water was added to the reaction mixture and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and then dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and the obtained residue was washed with hexane to give compound a15 (1.4 g, 94% yield).

(502) .sup.1H NMR (CDCl.sub.3) : 1.46 (d, J=8.0 Hz, 6H), 3.39 (m, 1H), 6.30 (bs, 1H), 6.96 (dd, J=8.0, 4.0 Hz, 1H), 7.30 (d, J=4.0 Hz, 1H), 7.79 (d, J=8.0 Hz, 1H).

(503) [M+H]=194.2, Method Condition 2: retention time 1.52 minutes

(504) Step 3 Preparation of Compound a16

(505) Compound a15 was dissolved in DMF (30 mL) and, N-chlorosuccinimide (2.3 g, 17 mmol) was added, and the mixture was stirred at 50 C. for 4 hours. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with aqueous ammonium chloride and brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give compound a16 (3.5 g, 88% yield).

(506) .sup.1H NMR (CDCl.sub.3) : 1.47 (d, J=8.0 Hz, 6H), 3.39 (m, 1H), 5.67 (s, 1H), 7.15 (d, J=8.0 Hz, 1H), 7.77 (d, J=8.0 Hz, 1H).

(507) [M+H]=228.9, Method Condition 2: retention time 1.91 minutes

(508) Step 4 Preparation of Compound I-038

(509) Compounds a8 (30 mg, 0.11 mmol) was dissolved in 1,4-dioxane (1.0 mL) then, the compound 16 (37 mg, 0.16 mmol), copper iodide (6.3 mg, 0.033 mmol), N,N-dimethyl glycine (10 mg, 0.098 mmol) and cesium carbonate (0.11 g, 0.33 mmol) were added and the mixture was stirred at 130 C. for 1 hour Water was added and the mixture was extracted with chloroform. The solvent was distilled off under reduced pressure, and the obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to afford Compound I-038 (26 mg, 57% yield).

(510) .sup.1H-NMR (CDCl.sub.3) : 1.29 (d, J=6.8 Hz, 3H) 1.49 (d, J=6.8 Hz, 6H) 1.99 (s, 3H) 3.36-3.49 (m, 1H) 4.24-4.33 (m, 2H), 4.36-4.48 (m, 1H), 5.69-5.80 (m, 1H), 7.24-7.31 (m, 1H), 7.77 (s, 1H), 7.89 (d, J=8.7 Hz, 1H), 8.01 (s, 1H).

(511) [M+H]=421.1, Method Condition 4: retention time 2.62 minutes

Example 5

Preparation of Compound I-046

(512) ##STR00087##
Step 1 Preparation of Compound a18

(513) Compound a17 (1.0 g, 4.4 mmol; J. Org. Chem. 2004, 69, 7694) was dissolved in DMF (15 mL) and sodium hydride (0.26 g, 6.6 mmol) was added under ice-cooling and the mixture was stirred at room temperature for 30 minutes. THF (3.5 mL) solution of (S)-3-benzyl-4-methyl-1,2,3-oxathiazolidine-2,2-dioxide (1.6 g, 4.4 mmol) was to the reaction solution under ice-cooling, and the mixture was stirred at room temperature for 2 hours. 2 mol/L hydrochloric acid aqueous solution (8.8 mL) was added to the reaction solution under ice-cooling, and the mixture was stirred at room temperature for 1 hour. 2 mol/L sodium hydroxide solution (18 mL) was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The solvent was distilled off under reduced pressure, and the obtained residue was purified by amino silica gel column chromatography (hexane-ethyl acetate) to give Compound a18 (1.6 g, 71% yield).

(514) .sup.1H NMR (CDCl.sub.3) : 1.06 (m, 12H), 1.37 (m, 2H), 1.51 (m, 2H), 1.67 (m, 2H), 1.79 (m, 2H), 2.94 (m, 1H), 3.22 (m, 1H), 3.28 (t, J=8.5 Hz, 1H), 3.41 (dd, J=9.3, 4.3 Hz, 1H), 3.77 (d, J=12.8 Hz, 1H), 3.78 (m, 1H), 3.90 (d, J=12.8 Hz, 1H), 7.30-7.41 (m, 11H), 7.66 (d, J=7.9 Hz, 4H).

(515) [M+H]=502.2, Method Condition 2: retention time 2.15 minutes

(516) Step 2 Preparation of Compound a19

(517) Compounds a18 (0.65 g, 1.3 mmol) was dissolved in methanol (6.5 mL), palladium hydroxide (0.16 g, 1.2 mmol) and ammonium formate (0.24 g, 3.9 mmol) were added and the mixture was refluxed for 4 hours. A sodium hydroxide solution was added to the reaction solution and the mixture was extracted with ethyl acetate. The organic layer was washed with brine and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and the obtained residue was dissolved in methylene chloride (3.2 mL). Acetic anhydride (0.13 mL, 1.4 mmol) and triethylamine (0.18 mL, 1.3 mmol) were added and the mixture was stirred at room temperature for 30 minutes. Water was added to the reaction mixture and the mixture was extracted with ethyl acetate. The organic layer was washed with brine and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, 1 mol/L tetrabutylammonium fluoride (1.9 mL, 1.9 mmol) was added to the obtained residue and the mixture was stirred at 70 C. for 10 hours. The reaction mixture was distilled off under reduced pressure, and the obtained residue was purified by silica gel column chromatography (chloroform-methanol) to give Compound a19 (0.27 g, 98% yield).

(518) .sup.1H NMR (CDCl.sub.3) : 1.19 (d, J=6.7 Hz, 3H), 1.44-1.60 (m, 2H), 1.60-1.72 (m, 4H), 1.76-1.90 (m, 2H), 1.97 (s, 3H), 3.37-3.40 (m, 1H), 3.31-3.46 (m, 2H), 3.68-3.80 (m, 1H), 4.14 (bs, 1H), 5.94 (bs, 1H).

(519) [M+H]=216.2, Method Condition 2: retention time 0.79 minutes

(520) Step 3 Preparation of Compound I-046

(521) Compound a19 (22 mg, 0.10 mmol) was dissolved in THF (1.0 mL) and Compound 15 (27 mg, 0.12 mmol), triphenylphosphine (34 mg, 0.13 mmol) and dimethyloxyethylazodicarboxylate (30 mg, 0.13 mmol) was added and the mixture was with stirred at room temperature for 3 hours. Water was added to the reaction mixture and the mixture was extracted with ethyl acetate. The organic layer was washed with brine and dried over anhydrous magnesium sulfate. The solvent was distilling off under reduced pressure and the obtained residue was purified by silica gel column chromatography (chloroform-methanol) to give Compound I-046 (15 mg, 35% yield).

(522) .sup.1H-NMR (CDCl.sub.3) : 1.19 (d, J=6.8 Hz, 3H), 1.42-1.54 (m, 8H), 1.61-1.75 (m, 2H) 1.98 (s, 3H), 2.01-2.11 (m, 4H), 3.32-3.50 (m, 4H), 4.08-4.20 (m, 1H), 4.34-4.47 (m, 1H), 5.60-5.71 (m, 1H), 7.13 (d, J=9.0 Hz, 1H), 7.78 (d, J=9.0 Hz, 1H).

(523) [M+H]=399.5, Method Condition 4: retention time 2.28 minutes

Example 6

Preparation of Compound I-075

(524) ##STR00088##
Step 1 Preparation of Compound a21

(525) Compounds a20 (0.53 g, 2.6 mmol) was dissolved in DMF (5.0 mL) and THF (2.5 mL), sodium hydride (0.13 g, 3.3 mmol) was added under ice-cooling and the mixture was stirred for 30 minutes under ice-cooling. THF (2.5 mL) solution of (S)-3-benzyl-4-methyl-1,2,3-oxathiazolidine-2,2-dioxide (0.50 g, 2.2 mmol) was to the reaction solution under ice-cooling, and the mixture was stirred at room temperature for 2 hours. 2 mol/L hydrochloric acid aqueous solution (10 mL) was added to the reaction solution under ice-cooling, and the mixture was stirred at room temperature for 1 hour. 2 mol/L sodium hydroxide solution (10 mL) was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The reaction solvent was distilled off under reduced pressure, and the obtained residue was purified by amino silica gel column chromatography (chloroform-methanol) to give Compound a21 (0.53 g, 95% yield).

(526) .sup.1H-NMR (CDCl.sub.3) : 1.06 (d, J=6.3 Hz, 3H), 1.91-1.78 (m, 2H), 2.76-2.62 (m, 2H), 2.95-2.85 (m, 1H) 3.32-3.17 (m, 2H), 3.56-3.46 (m, 1H), 3.78-3.67 (m, 1H), 3.96-3.83 (m, 2H), 7.37-7.21 (m, 5H).

(527) [M+H]=236.5, Method Condition 4: retention time 0.66 minutes

(528) Step 2 Preparation of Compound a22

(529) Compounds a19 (0.51 g, 2.1 mmol) was dissolved in methanol (2.5 mL), palladium hydroxide (0.30 g, 2.2 mmol) was added and the mixture was stirred for 1 hour under a hydrogen stream. Acetic anhydride (0.60 mL, 4.6 mmol) was added to the reaction solution and the mixture was stirred at room temperature overnight. 2 mol/L hydrochloric acid aqueous solution (10 mL) was added to the reaction solution under ice-cooling, and the mixture was stirred at room temperature for 1 hour. A saturated sodium bicarbonate solution was added to the mixture and the mixture was extracted with chloroform. The organic layer was washed with brine and dried over anhydrous magnesium sulfate. The reaction solvent was distilled off under reduced pressure, and the obtained residue was purified by silica gel column chromatography (chloroform-methanol) to give Compound a22 (0.24 g, 61% yield).

(530) 1H-NMR (CDCl.sub.3) : 1.18 (d, J=6.8 Hz, 3H), 1.82-1.92 (m, 2H), 1.97 (s, 3H), 2.66-2.76 (m, 2H), 3.27 (dd, J=9.4, 3.9 Hz, 1H), 3.33 (dd, J=9.4, 4.1 Hz, 1H), 3.50-3.59 (m, 1H), 3.89-4.00 (m, 1H), 4.08-4.17 (m, 1H), 5.62-5.77 (m, 1H)

(531) [M+H]=188.4, Method Condition 4: retention time 0.51 minutes

(532) Step 3 Preparation of Compound I-075

(533) Compounds a22 (30 mg, 0.16 mmol) was dissolved in THF (1 mL), Compound a11 (55 mg, 0.24 mmol), triphenylphosphine (84 mg, 0.32 mmol) and diisopropyl azodicarboxylate (0.17 mL, 0.32 mmol) were added, and the mixture was stirred at room temperature. Water was added to the reaction mixture and the mixture was extracted with ethyl acetate. The organic layer was washed with brine and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the obtained residue was purified by reverse phase column chromatography to give Compound I-075 (30 mg, 47% yield).

(534) .sup.1H-NMR (CDCl.sub.3) : 1.20 (d, J=6.8 Hz, 3H), 1.48 (t, J=7.2 Hz, 3H), 1.99 (s, 3H), 2.38-2.59 (m, 4H), 3.27-3.42 (m, 2H), 4.09-4.21 (m, 1H), 4.22-4.33 (m, 1H), 4.58 (q, J=7.1 Hz, 2H), 4.84-4.96 (m, 1H), 5.55-5.72 (m, 1H), 6.80 (d, J=8.8 Hz, 1H), 7.47 (d, J=8.8 Hz, 1H).

(535) [M+H]=399.5, Method Condition 4: retention time 2.28 minutes

Example 7

Preparation of Compound a26

(536) ##STR00089##
Step 1 Preparation of Compound a24

(537) 2,5-Dibromo-thiazole (8.6 g, 35 mmol) and Compound a23 (6.0 g, 38 mmol) were dissolved in DMF (90 mL), and potassium carbonate (9.8 g, 71 mmol) was added, and the mixture was stirred at 105 C. for 3 hours. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and then dried with anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to give compound a24 (12 g, 100% yield).

(538) .sup.1H NMR (CDCl.sub.3) : 3.81 (s, 3H), 6.84 (dd, J=8.9, 3.0 Hz, 1H), 7.00 (d, J=3.0 Hz, 1H), 7.11 (s, 1H), 7.23 (d, J=8.9 Hz, 1H).

(539) Step 2 Preparation of Compound a25

(540) Under a nitrogen atmosphere dichloromethane (240 mL) solution of Compound a22 (12 g, 37 mmol) was cooled to 78 C. with dry ice-acetone. 1.0 mol/L boron tribromide (150 mL, 150 mmol) was added dropwise in a reaction solution, and the mixture was raised to room temperature over 3 hours. The reaction mixture was poured into saturated sodium bicarbonate solution, the mixture was stirred, and extracted with ethyl acetate. The organic layer was washed with saturated brine, and then dried with anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to give compound a25 (12 g, 100% yield).

(541) .sup.1H NMR (DMSO-d6) : 6.82 (dd, J=8.9, 2.9 Hz, 1H), 6.97 (d, J=2.9 Hz, 1H), 7.37 (d, J=8.9 Hz, 1H), 7.40 (s, 1H), 10.17 (s, 1H).

(542) Step 3 Preparation of Compound a26

(543) Compound a25 (6.0 g, 20 mmol) was dissolved in DMF (15 mL) and potassium carbonate (4.1 g, 29 mmol) and (bromomethyl) cyclopropane (2.9 mL, 29 mmol) were added, and the mixture was stirred at 80 C. for 7 hours. Water was added to the reaction mixture, and the mixture was extracted with diethyl ether. The organic layer was washed with saturated brine, and then dried with anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give compound a26 (6.4 g, 96% yield).

(544) .sup.1H NMR (CDCl.sub.3) : 0.38-0.32 (m, 2H), 0.70-0.63 (m, 2H), 1.33-1.20 (m, 1H), 3.78 (d, J=7.0 Hz, 2H), 6.84 (dd, J=9.0, 2.9 Hz, 1H), 6.99 (d, J=2.9 Hz, 1H), 7.11 (s, 1H), 7.22 (d, J=9.0 Hz, 1H).

Example 8

Preparation of Compound a28

(545) ##STR00090##

(546) Compound a27 (40 g, 0.20 mol), N,O-dimethylhydroxylamine hydrochloride (23 g, 0.24 mol), HATU (112 g, 0.30 mol) were dissolved in DMF (0.60 L) and triethylamine (60 g, 0.60 mol) was added and the mixture was stirred at room temperature overnight. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and then dried with anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give compound a28 (34 g, 69% yield).

(547) .sup.1H NMR (CDCl.sub.3) : 1.24 (d, J=6.4 Hz, 3H), 1.43 (s, 9H), 2.53-2.74 (m, 2H), 3.18 (s, 3H), 3.69 (s, 3H), 4.06-4.11 (m, 1H), 5.32 (bs, 1H).

Example 9

Preparation of Compound I-002

(548) ##STR00091##
Step 1 Preparation of Compound a29

(549) Compounds of a26 (1.0 g, 2.8 mmol) was dissolved in THF (20 mL) and cooled to 78 C. 2.6 mol/L butyl lithium solution in hexane (2.2 mL, 5.6 mmol) was added to the mixture and the mixture was stirred for 30 minutes at 78 C. THF (5.0 mL) solution of Compound a28 (0.75 g, 3.1 mmol) was added to the reaction mixture, and the mixture was stirred at 78 C. for 5 minutes. The mixture was further gradually warmed to room temperature, and stirred for 1 hour. A saturated aqueous ammonium chloride solution and saturated brine was added to the reaction solution the mixture was extracted with ethyl acetate, and the organic layer was dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, the obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give compound a29 (0.30 g, 23% yield).

(550) .sup.1H NMR (CDCl.sub.3) : 0.36 (m, 2H), 0.67 (m, 2H), 1.25 (d, J=6.7 Hz, 3H), 1.42 (s, 9H), 2.86 (dd, J=15.1, 6.8 Hz, 1H), 3.16 (dd, J=15.1, 3.3 Hz, 1H), 3.80 (d, J=7.0 Hz, 2H), 4.10 (m, 1H), 4.88 (bs, 1H), 6.87 (dd, J=9.0, 3.0 Hz, 1H), 7.01 (d, J=3.0 Hz, 1H), 7.22 (d, J=9.0 Hz, 1H), 7.89 (s, 1H).

(551) Step 2 Preparation of Compound I-002

(552) Compound a29 (0.30 g, 0.64 mmol) was dissolved in 1,4-dioxane (3.0 mL), 4 mol/L hydrochloric acid in 1,4-dioxane (1.6 mL, 6.4 mmol) was added and the mixture was stirred at room temperature for 2 hours. The solvent was distilled off under reduced pressure, the obtained reaction product was dissolved in chloroform (3.0 mL), pyridine (0.16 mL, 1.9 mmol) and acetic anhydride (0.24 mL, 2.6 mmol) was added, and the mixture was stirred at 60 C. for 1 hour. A saturated aqueous sodium hydrogen carbonate solution was added, and the mixture was extracted with chloroform, and then dried with anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, the obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to afford Compound I-002 (0.21 g, 81% yield).

(553) .sup.1H NMR (CDCl.sub.3) : 0.36 (m, 2H), 0.66 (m, 2H), 1.27 (d, J=6.8 Hz, 3H), 1.95 (s, 3H), 2.93 (dd, J=15.8, 6.0 Hz, 1H), 3.16 (dd, J=15.8, 4.5 Hz, 1H), 3.80 (d, J=7.0 Hz, 2H), 4.40 (m, 1H), 6.04 (bd, J=7.8 Hz, 1H), 6.87 (dd, J=8.8, 2.8 Hz, 1H), 7.02 (d, J=2.8 Hz, 1H), 7.22 (d, J=8.8 Hz, 1H), 7.86 (s, 1H).

(554) [M+H]=409.3, Method Condition 2: retention time 2.15 minutes

Example 10

Preparation of Compound I-004

(555) ##STR00092##
Step 1 Preparation of Compound a31

(556) Compound a30 (0.5 g, 2.9 mmol) was dissolved in 1,4-dioxane (10 mL), Boc-L-alaninol (0.76 g, 4.3 mmol), triphenylphosphine (1.1 g, 4.3 mmol) and dimethyloxyethylazodicarboxylate (1.0 g, 4.3 mmol) were added, and, the mixture was stirred at 60 C. for 1 hour. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give compound a31 (0.82 g, 86% yield).

(557) .sup.1H NMR (CDCl.sub.3) : 1.29 (d, J=6.8 Hz, 3H), 1.45 (s, 9H), 3.96 (bs, 2H), 4.06 (bs, 1H), 4.68 (bs, 1H), 7.13 (dd, J=8.7, 2.6 Hz, 1H), 7.37 (d, J=8.7 Hz, 1H), 8.07 (d, J=2.6 Hz, 1H).

(558) [M+H]=333.1, Method Condition 2: retention time 2.10 minutes

(559) Step 2 Preparation of Compound a32

(560) Compound a31 (0.11 g, 0.34 mmol) was dissolved in 1,4-dioxane (2.0 mL), 2-chloro-4-propyl phenol (87 mg, 0.51 mmol), 2-dimethyl-amino-acetic acid (32 mg, 0.31 mmol), copper iodide (20 mg, 0.10 mmol) and cesium carbonate (0.33 g, 1.0 mmol) were added, and, the mixture was stirred under microwave irradiation at 150 C. for 75 minutes. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with brine and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give compound a32 (81 mg, 56% yield).

(561) .sup.1H NMR (CDCl.sub.3) : 0.96 (t, J=7.3 Hz, 3H), 1.30 (d, J=6.8 Hz, 3H), 1.61-1.70 (m, 2H), 1.99 (s, 3H), 2.57 (t, J=7.5 Hz, 2H), 3.89-3.98 (m, 2H), 4.37 (m, 1H), 5.71 (bd, J=7.3 Hz, 1H), 6.89 (d, J=9.0 Hz, 1H), 7.05-7.13 (m, 2H), 7.31 (dd, J=9.0, 3.0 Hz, 1H), 7.80 (bd, J=2.8 Hz, 1H).

(562) [M+H]=422.0, Method Condition 2: retention time 2.88 minutes

(563) Step 3 Preparation of Compound I-004

(564) Compound a32 (78 mg, 0.19 mmol) was dissolved in 1,4-dioxane (10 mL) and then, 4 mol/L hydrochloric acid in 1,4-dioxane (0.93 mL, 3.7 mmol) was added, and the mixture was stirred at room temperature for 1 hour. A saturated aqueous sodium hydrogen carbonate solution and water were added to the reaction mixture, and the mixture was extracted with ethyl acetate, and dried with anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, the obtained reaction product was dissolved in chloroform (3.0 mL), pyridine (0.045 mL, 0.56 mmol) and acetic anhydride (0.053 mL, 0.56 mmol) were added, and the mixture was stirred at room temperature for 1 hour. The solvent was distilled off under reduced pressure, and the obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to afford Compound I-004 (37 mg, 56% yield).

(565) .sup.1H NMR (CDCl.sub.3) : 0.96 (t, J=7.3 Hz, 3H), 1.30 (d, J=6.8 Hz, 3H), 1.61-1.70 (m, 2H), 1.99 (s, 3H), 2.57 (t, J=7.5 Hz, 2H), 3.89-3.98 (m, 2H), 4.37 (m, 1H), 5.71 (bd, J=7.3 Hz, 1H), 6.89 (d, J=9.0 Hz, 1H), 7.05-7.13 (m, 2H), 7.31 (dd, J=9.0, 3.0 Hz, 1H), 7.80 (bd, J=2.8 Hz, 1H).

(566) [M+H]=364.2, Method Condition 2: retention time 2.32 minutes

Example 11

Preparation of Compound I-005

(567) ##STR00093##
Step 1 Preparation of Compound a34

(568) Compound a33 (0.50 g, 2.3 mmol) was dissolved in 1,4-dioxane (10 mL), Boc-L-alaninol (0.60 g, 3.4 mmol), triphenylphosphine (0.89 g, 3.4 mmol) and dimethyloxyethylazodicarboxylate (0.80 g, 3.4 mmol) were added, and, the mixture was stirred at room temperature. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give compound a34 (0.42 g, 49% yield).

(569) .sup.1H NMR (CDCl.sub.3) : 1.27 (d, J=7.0 Hz, 3H), 1.45 (s, 9H), 3.88-3.89 (m, 2H), 4.11 (bs, 1H), 4.71 (bs, 1H), 6.68 (d, J=7.3 Hz, 2H), 7.55 (d, J=7.3 Hz, 2H).

(570) Step 2 Preparation of Compound a35

(571) Compound a34 (0.20 g, 0.53 mmol) was dissolved in 1,4-dioxane (2.0 mL), 2-chloro-4-propyl phenol (0.14 g, 0.80 mmol), 2-dimethyl-amino-acetic acid (49 mg, 0.48 mmol), copper iodide (30 mg, 0.16 mmol) and cesium carbonate (0.52 g, 1.6 mmol) were added, and, the mixture was stirred under microwave irradiation at 150 C. for 75 minutes. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with brine and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give compound a35 (0.14 g, 63% yield).

(572) .sup.1H NMR (CDCl.sub.3) : 0.94 (t, J=7.5 Hz, 3H), 1.29 (d, J=6.8 Hz, 3H), 1.45 (s, 9H), 1.62 (m, 2H), 2.54 (t, J=7.5 Hz, 2H), 3.90-3.93 (m, 2H), 4.05 (bs, 1H), 4.79 (bs, 1H), 6.74-7.05 (m, 6H), 7.25-7.31 (m, 2H).

(573) Step 3 Preparation of Compound I-005

(574) Compound a35 (70 mg, 0.34 mmol) was dissolved in 1,4-dioxane (0.50 mL), 4 mol/L hydrochloric acid in 1,4-dioxane (2.5 mL, 10 mmol), and the mixture was stirred at room temperature for 3 hours. The solvent was evaporated under reduced pressure. The obtained residue was dissolved in chloroform (2.0 mL), pyridine (0.045 mL, 0.56 mmol) and acetic anhydride (0.053 mL, 0.56 mmol) were added, and the mixture was stirred at room temperature for 1 hour. The solvent was distilled off under reduced pressure, and the obtained residue was purified by preparative HPLC (0.1% formic acid-containing acetonitrile-water) to give Compound I-005 (19 mg, 46% yield).

(575) .sup.1H NMR (CDCl.sub.3) : 0.94 (t, J=7.3 Hz, 3H), 1.31 (d, J=6.9 Hz, 3H), 1.62 (m, 2H), 2.00 (s, 3H), 2.54 (t, J=7.6 Hz, 2H), 3.88-3.97 (m, 2H), 4.38 (m, 1H), 5.80 (bd, J=7.5 Hz, 1H), 6.79-7.05 (m, 6H), 7.25-7.27 (m, 2H).

(576) [M+H]=362.3, Method Condition 3: retention time 2.56 minutes

Example 12

Preparation of Compound I-011

(577) ##STR00094##
Step 1 Preparation of Compound a37

(578) Compound a36 (0.34 g, 2.0 mmol) was dissolved in 1,4-dioxane (8.0 mL), benzyl ((2S,3R)-3-hydroxy-butan-2-yl) carbamate (0.40 g, 1.8 mmol; Tetrahedron Letters, 1998, 39, 5195-5198), triphenylphosphine (0.66 g, 2.3 mmol) and dimethyloxyethylazodicarboxylate (0.55 g, 2.3 mol) were added, and the mixture was stirred at 50 C. for 30 minutes. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, the obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give compound a37 (0.26 g, 39% yield).

(579) .sup.1H NMR (CDCl.sub.3) : 1.19 (d, J=6.9 Hz, 3H), 1.29 (d, J=6.2 Hz, 3H), 3.95 (bs, 2H), 5.07-5.21 (m, 4H), 6.58 (d, J=8.4 Hz, 1H), 7.34 (m, 5H), 7.60 (d, J=8.4 Hz, 1H), 8.14 (s, 1H).

(580) [M+H]=380.7, Method Condition 2: retention time 2.50 minutes

(581) Step 2 Preparation of Compound a38

(582) Compound a37 (0.13 g, 0.34 mmol) was dissolved in 1,4-dioxane (2.0 mL), 2-chloro-4-propyl phenol (86 mg, 0.51 mmol), 2-dimethyl amino acetic acid (31 mg, 0.30 mmol), copper iodide (19 mg, 0.10 mmol) and cesium carbonate (0.33 g, 1.0 mmol) were added, and, the mixture was stirred under microwave irradiation at 150 C. for 75 minutes. Water and 28% aqueous ammonia were added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with brine and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give compound a38 (28 mg, 18% yield).

(583) [M+H]=469.2, Method Condition 3: retention time 3.23 minutes

(584) Step 3 Preparation of Compound I-011

(585) Compound a38 (27 mg, 0.058 mmol) was dissolved in methanol (10 mL), 10% palladium on carbon (50% water) (27 mg) was added, and the mixture was stirred at room temperature under hydrogen atmosphere of 1 atm for 1 hour. Triethylamine (1.0 mL) was added to the reaction mixture, and the mixture was filtered through Celite. The solvent was distilled off under reduced pressure, and the obtained residue was dissolved in DMF (1 mL). Pyridine (0.023 mL, 0.29 mmol) and acetic anhydride (0.027 mL, 0.29 mmol) were added and the mixture was stirred overnight at room temperature. The obtained reaction solution was purified by preparative HPLC (0.1% formic acid-containing acetonitrile-water) to give Compound I-011 (4.0 mg, 18% yield).

(586) 1H NMR (CDCl.sub.3) : 0.94 (t, J=7.0 Hz, 3H), 1.20 (d, J=6.8 Hz, 3H), 1.30 (d, J=6.2 Hz, 3H), 1.59-1.68 (m, 2H), 1.99 (s, 3H), 2.57 (t, J=7.5 Hz, 2H), 4.20 (m, 1H), 5.14 (m, 1H), 5.94 (bd, J=8.5 Hz, 1H), 6.70 (d, J=9.3 Hz, 1H), 6.85 (d, J=8.2 Hz, 2H), 7.01 (d, J=8.2 Hz, 2H), 7.27 (m, 2H), 7.85 (s, 1H).

(587) [M+H]=377.4, Method Condition 3: retention time 2.60 minutes

Example 13

Preparation of Compound I-0126

(588) ##STR00095##
Step 1 Preparation of Compound a39

(589) Compound a36 (1.5 g, 8.6 mmol) was dissolved in 1,4-dioxane (15 mL), Boc-L-alaninol (1.8 g, 10 mmol), triphenylphosphine (2.9 g, 11 mmol) and dimethyloxyethylazodicarboxylate (2.6 g, 11 mmol) were added and the mixture was stirred at room temperature for 1 hour. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, the obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give compound a39 (2.2 g, 76% yield).

(590) .sup.1H NMR (CDCl.sub.3) : 1.24 (d, J=6.8 Hz, 3H), 1.44 (s, 9H), 4.07 (bs, 1H), 4.22-4.23 (m, 2H), 4.76 (bs, 1H), 6.68 (d, J=8.5 Hz, 1H), 7.65 (d, J=8.5 Hz, 1H), 8.17 (s, 1H).

(591) [M+H]=333.1, Method Condition 2: retention time 2.35 minutes

(592) Step 2 Preparation of Compound a40

(593) Compound a39 was dissolved in 1,4-dioxane (4.0 mL), Compound 16 (0.21 g, 0.91 mmol), 2-dimethyl amino acetic acid (56 mg, 0.54 mmol), copper iodide (35 mg, 0.18 mmol) and cesium carbonate (0.59 g, 1.8 mmol) were added, and the mixture was stirred under microwave irradiation at 150 C. for 1 hour. Water and 28% aqueous ammonia were added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with brine and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give compound a40 (46 mg, 16% yield).

(594) [M+H]=478.1, Method Condition 2: retention time 2.95 minutes

(595) Step 3 Preparation of Compound I-012

(596) Compound a40 (46 mg, 0.096 mmol) and 1,4-dioxane (1.0 mL) and then 4 mol/L hydrochloric acid in 1,4-dioxane (0.48 mL, 1.9 mmol) was added and the mixture was stirred at room temperature for 30 minutes. The solvent was evaporated under reduced pressure. The residue was dissolved in DMF (1.0 mL) and pyridine (0.039 mL, 0.48 mmol) and acetic anhydride (0.045 mL, 0.48 mmol) were added and the mixture was stirred at room temperature for 1 hour. The residue was purified by preparative HPLC (0.1% formic acid-containing acetonitrile-water) to give Compound I-012 (25 mg, 62% yield).

(597) .sup.1H NMR (CDCl.sub.3) : 1.27 (d, J=7.0 Hz, 3H), 1.50 (d, J=7.3 Hz, 3H), 1.97 (s, 3H), 3.42 m, J=6.8 Hz, 2H), 4.24-4.38 (m, 3H), 5.93 (bd, J=6.0 Hz, 1H), 6.76 (d, J=8.8 Hz, 1H), 7.08 (d, J=8.8 Hz, 1H), 7.28-7.31 (m, 1H), 7.80 (d, J=8.8 Hz, 1H), 7.89 (bd, J=2.3 Hz, 1H).

(598) [M+H]=420.3, Method Condition 3: retention time 2.39 minutes

Example 14

Preparation of Compound I-106

(599) ##STR00096##
Step 1 Preparation of Compound a42

(600) Compound a41 (1.12 g, 6.5 mmol) was dissolved in 1,4-dioxane (15 mL), t-butyl ((1S,2R)-2-hydroxy-cyclopentyl) carbamate (1.0 g, 5.0 mmol), triphenylphosphine (1.7 g, 6.5 mmol) and dimethyl oxyethyl azodicarboxylate (1.5 g, 6.5 mmol) were added and the mixture was stirred at 65 C. for 1 hour. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the contained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give compound a42 (1.4 g, 77% yield).

(601) .sup.1H NMR (CDCl.sub.3) : 1.41 (s, 9H), 1.45-1.54 (m, 1H), 1.71-1.85 (m, 3H), 2.10-2.15 (m, 1H), 2.23-2.26 (m, 1H), 3.97 (m, 1H), 4.91 (m, 1H), 5.13-5.14 (m, 1H), 6.67 (d, J=8.7 Hz, 1H), 7.63 (d, J=8.7 Hz, 1H), 8.15 (s, 1H).

(602) [M+H]=358.3, Method Condition 4: retention time 2.57 minutes

(603) Step 2 Preparation of Compound a43

(604) Compound a42 was dissolved in 1,4-dioxane (8.0 mL), Compound a16 (0.38 g, 1.68 mmol), 2-dimethyl amino acetic acid (104 mg, 1.01 mmol), copper iodide (64 mg, 0.34 mmol) and cesium carbonate (1.09 g, 3.36 mmol) were added, and the mixture was stirred under microwave irradiation at 150 C. for 70 minutes. Water and 28% aqueous ammonia were added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with brine and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give compound a43 (135 mg, 24% yield).

(605) [M+H]=504.1, Method Condition 2: retention time 3.08 minutes

(606) Step 3 Preparation of Compound I-106

(607) Compound a43 was dissolved in 1,4-dioxane (1.0 mL) and 4 mol/L hydrochloric acid in 1,4-dioxane (1.34 mL, 5.36 mmol) was added and the mixture was stirred at room temperature for 30 minutes. The solvent was evaporated under reduced pressure. The residue was dissolved in DMF (1.0 mL) and pyridine (0.108 mL, 1.34 mmol) and acetic anhydride (0.127 mL, 1.34 mmol) was added and the mixture was stirred at room temperature for 1 hour. The residue was purified by preparative HPLC (0.1% formic acid-containing acetonitrile-water) to afford Compound I-106 (34 mg, 29% yield).

(608) .sup.1H NMR (CDCl.sub.3) 1.46 (m, 1H), 1.50 (d, J=7.0 Hz, 6H), 1.70-1.85 (m, 3H), 1.93 (s, 3H), 2.09-2.20 (m, 1H), 2.33-2.39 (m, 3H), 3.37-3.47 (m, 1H), 4.12-4.19 (m, 1H), 5.15-5.22 (m, 1H), 6.40 (m, 1H), 6.77 (d, J=9.0 Hz, 1H), 7.07 (d, J=8.8 Hz, 1H), 7.28-7.29 (m, 1H), 7.80 (d, J=8.8 Hz, 1H), 7.86-7.87 (m, 1H).

(609) [M+H]=446.0, Method Condition 4: retention time 2.58 minutes

Example 15

Preparation of Compound c7

(610) Step 1 Preparation of Compound c1

(611) ##STR00097##

(612) Compound c0 (4.0 g, 20.7 mmol) was dissolved in THF (20 mL), and triethylamine (3.74 mL, 26.9 mmol) and 1.0 mol/L methyl amine THF solution (11.4 mL, 22.8 mmol) were added to the mixture while cooling in ice, and the mixture was stirred at room temperature for 1 hour. 1.0 mol/L methyl amine THF solution (34.2 mL, 68.4 mmol) was further added to the mixture, and the mixture was stirred for one and half hours. In addition, 1.0 mol/L methyl amine THF solution (18.0 mL, 36.0 mmol) was added to the mixture, and the mixture was stirred for 15 hours. Water was added to the mixture while cooling in ice, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was condensed under reduced pressure to afford a crude compound c1 (3.50 g, yield 90%).

(613) .sup.1H-NMR (CDCl.sub.3) : 3.06 (d, J=4.8 Hz, 3H), 6.75 (s, 1H), 8.17 (brs, 1H), 9.02 (s, 1H).

(614) [M+H]=187.95, Method Condition 3: retention time 1.45 min

(615) Step 2 Preparation of Compound c2

(616) ##STR00098##

(617) N-chlorosuccinimide (615 mg, 4.61 mmol) was added to the DMF solution (10 mL) of Compound c1 (786 mg, 4.19 mmol), and the mixture was stirred for 2.5 hours at room temperature. Distilled water (50 mL) was added to the mixture, and the mixture was extracted with ethyl acetate twice. The organic layer was washed with 50 mL of distilled water five times and 50 mL of saturated brine once. The organic layer was dried over anhydrous sodium sulfate. The solvent was condensed under reduced pressure to afford a compound c2 (960 mg, quant).

(618) .sup.1H-NMR (CDCl.sub.3) : 3.29 (d, J=5.5 Hz, 3H), 7.62 (br s, 1H), 8.78 (s, 1H).

(619) Step 3 Preparation of Compound c3

(620) ##STR00099##

(621) Cyclopropanol (157 mg, 2.70 mmol), 18-crown-6 (714 mg, 2.70 mmol) and cesium carbonate (1.761 g, 5.40 mmol) were added to the THF solution (4 mL) of Compound c2 (400 mg, 1.802 mmol), and the mixture was refluxed for 7 hours. The mixture was diluted with ethyl acetate (20 mL) and filtered through celite. The filtrate was condensed under reduced pressure, and the residue was purified by silica gel chromatography (hexane:ethyl acetate=5:1) to afford Compound c3 (140 mg, yield 32%) as yellow solid.

(622) .sup.1H-NMR (CDCl.sub.3) : 0.82-0.85 (m, 4H), 3.33 (d, J=5.5 Hz, 3H), 4.40-4.45 (m, 1H), 7.84 (br s, 1H), 8.86 (s, 1H).

(623) Step 4 Preparation of Compound c4

(624) ##STR00100##

(625) Diluted water (0.5 mL), reduced iron (128 mg, 2.298 mmol) and ammonium chloride (123 mg, 2.298 mmol) were added to the ethanol solution (2 mL) of Compound a3, and the mixture was stirred at 60 C. for 4 hours. The mixture was filtered through celite and the filtrate was condensed under reduced pressure. 1,1-thiocarbonyl diimidazole (123 mg, 0.690 mmol) was added to THF solution (2 mL) of the obtained residue, the mixture was stirred at room temperature for 1.5 hours. Potassium carbonate (318 mg, 2.298 mmol) and methyl iodide (0.072 ml, 1.149 mmol) were added to the mixture, the mixture was stirred at room temperature for further 12 hours. The mixture was filtered through celite. The filtrate was condensed under reduced pressure, and the residue was purified by silica gel chromatography (hexane:ethyl acetate=2:1) to afford Compound c4 (68 mg, yield 44%) as white solid.

(626) .sup.1H-NMR (d6-DMSO) : 0.65-0.81 (m, 4H), 2.73 (s, 3H), 3.88 (s, 3H), 4.32-4.36 (m, 1H), 8.40 (s, 1H).

(627) Step 5 Preparation of Compound c5

(628) ##STR00101##

(629) m-CPBA (131 mg, 0.530 mmol) was added to the dichlorometane (1 mL) solution of Compound c4 (65 mg, 0.241 mmol), and the mixture was stirred at room temperature for 2 hours. A saturated sodium bicarbonate aqueous solution (10 mL) was added to the mixture, and the mixture was extracted with ethyl acetate (10 mL) twice. The organic layer was washed with saturated sodium bicarbonate aqueous solution (10 mL) three times, and saturated brine (10 mL) once. The organic layer was dried over anhydrous sodium sulfate. The solvent was condensed under reduced pressure, and the residue was purified by silica gel chromatography (hexane:ethyl acetate=1:1) to afford Compound c5 (65 mg, yield 89%) as white solid.

(630) .sup.1H-NMR (CDCl.sub.3) : 0.83-0.87 (m, 4H), 3.56 (s, 3H), 4.39 (s, 3H), 4.41-4.45 (m, 1H), 8.68 (s, 1H).

(631) Step 6 Preparation of Compound c7

(632) ##STR00102##

(633) Compound c6 (57.9 mg, 0.271 mmol) and tert-butoxy potassium (60.9 mg, 0.543 mmol) were successively added to the THF (1 mL) solution of Compound c5 (63 mg, 0.209 mmol) under ice-cooling. The reaction solution was stirred at 0 C. for 30 minutes A saturated ammonium chloride solution (10 ml) was added to the reaction mixture, and the mixture was extracted with ethyl acetate (10 ml) twice. The organic layers washed with distilled water (10 ml) twice once with saturated brine (10 ml), and dried over sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was sequentially purified by DNH column chromatography (hexane:ethyl acetate=1:2) and silica gel column chromatography (chloroform:methanol=10:1) to give compound c7 to (30 mg, 33%) by solidifying with ethyl acetate.

Example 16

Preparation of Compound c18

(634) Step 1 Preparation of Compound c9

(635) ##STR00103##

(636) To the THF (20 ml) solution of Compound c8 (2 g, 11.29 mmol), trimethylamine (3.44 ml, 24.85 mmol) and methylamine (33% ethanol solution, 1.547 ml, 12.42 mmol) were added sequentially while cooling in ice. The reaction mixture was stirred at 0 C. for 10 hours. A saturated brine was added to the reaction mixture, and the reaction mixture was extracted with ethyl acetate (100 ml) twice. The organic layer was dried over sodium sulfate. The solvent was condensed under reduced pressure to afford Compound c9 (2.2 g, 90% purity, 93%) as a mixture with Compound c10.

(637) .sup.1H-NMR (CDCl.sub.3) : 2.97 (d, J=5.0 Hz, 3H), 6.18-6.28 (m, 2H), 7.64 (s, 1H).

(638) Step 2 Preparation of Compound c11

(639) ##STR00104##

(640) N-chlorosuccinimide (4.62 g, 34.6 mmol) was added to the acetonitrile (40 ml) solution of Compound c9 (5.92 g, 90% purity, 28.35 mmol), and the mixture was stirred at 90 C. for 1 hour. The reaction mixture was condensed under reduced pressure, and the insoluble matter was filtered. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=5:1) to afford the mixture of Compounds c11 and c12 (2.25 g, 32%) as a yellow solid.

(641) .sup.1H-NMR (CDCl.sub.3) : 2.94 (d, J=5.5 Hz, 3H), 5.23 (s, 1H), 6.43 (dd, J=9.9, 8.5 Hz, 1H).

(642) Step 3 Preparation of Compound c13

(643) ##STR00105##

(644) To the THF (20 mL) solution of Compound c11 (2.25 g, 10.11 mmol), 2,2-difluoroethanol (0.704 ml, 11.12 mmol), potassium carbonate (3.07 g, 22.24 mmol) and 18-crown-6 (8.02 g, 30.3 mmol) were added, and then the mixture was refluxed for 1 hour. Distilled water (30 ml) was added to the reaction mixture, and the reaction mixture was extracted with ethyl acetate (30 ml) twice. The organic layer was washed with distilled water (30 ml) twice, and saturated brine (30 ml) once. The organic layer was dried over sodium sulfate, and the solvent was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=5:1) to afford Compound c13 as the mixture with Compound c14 (1.33 g, c13:c14=2:1, 31%).

(645) Step 4 Preparation of Compound c15

(646) ##STR00106##

(647) To the THF (20 ml) solution of the mixture of Compound c13 and Compound c14 (1.33 g, 4.67 mmol, c13:c14=2:1), 5% Pt/C (50% wet, 300 mg, 0.038 mmol) was added, and the mixture was stirred for 14 hours under hydrogen atmosphere. After filtered by celite, the solvent was concentrated under reduced pressure. Imidazole (0.636 g, 9.35 mmol) and 1,1-thiocarbonyl diimidazole (0.999 g, 5.61 mmol) were added to the THF (20 ml) solution of the residue, and the mixture was refluxed for 2 hours. Distilled water was added to the reaction mixture, and the reaction mixture was extracted with ethyl acetate. The organic layer was washed with brine twice, and dried over sodium sulfate. The solvent was concentrated under reduced pressure. The residue was suspended with ethyl acetate, and filtered to afford Compound c15 as a mixture with Compound c16 (1.05 g, c15:c16=2:1, 50%).

(648) Step 5 Preparation of Compound c17

(649) ##STR00107##

(650) To the THF (10 ml) solution of the mixture of Compound c15 and Compound c16 (988 mg, 3.33 mmol, c15:c16=2:1), potassium carbonate (1013 mg, 7.33 mmol) and methyl iodide (0.229 ml, 3.66 mmol) were added, and the mixture was stirred at room temperature for 3 hours. After filtered by celite, the solvent was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=3:1) to afford Compound c17 (581 mg, 56%) as a white solid.

(651) .sup.1H-NMR (CDCl.sub.3) : 2.80 (s, 3H), 4.00 (s, 3H), 4.23 (td, J=13.0, 4.1 Hz, 2H), 6.14 (tt, J=55.0, 4.1 Hz, 1H), 6.68 (d, J=10.7 Hz, 1H).

(652) Step 6 Preparation of Compound c18

(653) ##STR00108##

(654) To the dichloromethane (10 ml) solution of Compound c17 (580 mg, 1.867 mmol), m-chloroperbenzoic acid (1012 mg, 4.11 mmol) was added at room temperature for 5 hours. Distilled water (50 ml) was added to the reaction mixture, and the reaction mixture was extracted with ethyl acetate (50 ml) twice. The organic layer was washed with 1 mol/L sodium hydrate aqueous solution (50 ml) five times and saturated brine (50 ml) once. The organic layer dried over sodium sulfate, and then the solvent was concentrated under reduced pressure. The residue was suspended with ethyl acetate, and filtered to afford Compound c18 (640 mg, 100%) as a white solid.

(655) .sup.1H-NMR (CDCl.sub.3) : 3.59 (s, 3H), 4.29 (td, J=12.8, 4.1 Hz, 2H), 4.45 (s, 3H), 6.16 (tt, J=54.8, 4.1 Hz, 1H), 6.85 (d, J=10.5 Hz, 1H).

Example 17

Preparation of Compound c26

(656) Step 1 Preparation of Compound c20

(657) ##STR00109##

(658) To the THF (50 ml) solution of Compound c19 (21.63 g, 111 mmol), potassium carbonate (33.7 g, 244 mmol) and methylamine (33% ethanol solution, 14.49 ml, 116 mmol) were sequentially added while cooling in ice, and the mixture was stirred at 0 C. for 20 minutes. After filtered by celite, the solvent was concentrated under reduced pressure. The residue was diluted with ethyl acetate (200 ml). The organic layer was washed with saturated brine (200 ml) three times, and dried with sodium sulfate. The solvent was concentrated under reduced pressure. To the THF (150 ml) solution of the obtained solid residue, potassium carbonate (30.6 g, 222 mmol), 2,2-difluoroethanol (7.02 ml, 111 mmol) and 18-crown-6 (35.2 g, 133 mmol) were added, and then the mixture was refluxed for 1 hour. After filtered by celite, the solvent was concentrated under reduced pressure. The residue was purified by silica gel chromatography (hexane:ethyl acetate=5:1) to afford Compound c20 (21.1 g, 71%) as a yellow solid.

(659) .sup.1H-NMR (CDCl.sub.3) : 3.18 (dd, J=6.9, 5.4 Hz, 3H), 4.26 (td, J=12.7, 4.0 Hz, 2H), 5.93-6.28 (m, 2H), 6.83 (s, 1H).

(660) Step 2 Preparation of Compound c21

(661) ##STR00110##

(662) To the ethanol (10 ml) suspension of Compound c21 (2.03 g, 7.57 mmol), THF (10 mL), zinc (2.475 g, 37.8 mmol) and ammonium chloride (2.025 g, 37.8 mmol) were added, and the mixture was stirred at room temperature for 2 hours. The reaction mixture was filtered by celite, and the solvent was concentrated under reduced pressure. To the THF (20 ml) solution of the obtained residue, imidazole (1.546 g, 22.71 mmol) and 1,1-thiocarbonyl diimidazole (1.619 g, 9.08 mmol) were added, and the mixture was stirred for 1 hour while refluxing. Potassium carbonate (2.092 g, 15.14 mmol) and methyl iodide (0.568 ml, 9.08 mmol) were added to the reaction solution, and the mixture was further stirred at room temperature for 3 hours. The reaction mixture was filtered by celite, and the solvent was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=2:1) to afford Compound c21 (1.83 g, 82%) as a white solid.

(663) .sup.1H-NMR (CDCl.sub.3) : 2.80 (s, 3H), 3.84 (s, 3H), 4.25 (td, J=13.1, 4.1 Hz, 2H), 6.10 (tt, J=55.0, 4.1 Hz, 1H), 6.66 (dd, J=10.5, 6.0 Hz, 1H).

(664) Step 3 Preparation of Compound c22

(665) ##STR00111##

(666) To the dichloromethane (30 ml) solution of Compound c21 (1.8 g, 6.12 mmol), m-chloroperbenzoic acid (3.32 g, 13.46 mmol) was added, and the mixture was stirred at room temperature for 3 hours. Distilled water (200 ml) was added to the reaction mixture, and the reaction mixture was extracted with ethyl acetate (200 ml) twice. The organic layer was washed with 0.1 mol/L sodium hydrate aqueous solution (200 ml) five times, and brine (200 ml) once. The organic layer was dried over sodium sulfate, and the solvent was concentrated under reduced pressure. The residue was suspended with ethyl acetate and filtered to afford Compound c22 (2 g, 100%) as a white solid.

(667) .sup.1H-NMR (CDCl.sub.3) : 3.58 (s, 3H), 4.29 (s, 3H), 4.32 (dt, J=4.0, 12.9 Hz, 2H), 6.12 (tt, J=54.8, 4.0 Hz, 1H), 6.84 (dd, J=10.3, 5.9 Hz, 1H).

(668) Step 4 Preparation of Compound c24

(669) ##STR00112##

(670) The compound c23 (145 mg, 0.674 mmol) was added to the THF (2 ml) suspension of tert-butoxy potassium (151 mg, 1.349 mmol) under ice-cooling. After the reaction mixture was stirred at 0 C. for 10 minutes, the THF (3 ml) solution of Compounds c22 (200 mg, 0.613 mmol) was added dropwise under ice-cooling. The mixture was stirred for a further 1 hour at 0 C. A saturated aqueous ammonium chloride solution (30 ml) was added to the mixture under ice-cooling. The reaction solution was extracted with ethyl acetate (30 ml) twice, with a saturated aqueous ammonium chloride solution (30 ml) once, and washed with saturated brine (30 ml) twice. The organic layer was dried with sodium sulfate, and the solvent was evaporated under reduced pressure.

(671) The residue was purified by DNH column chromatography (chloroform:methanol=10:1) and purified sequentially silica gel column chromatography (chloroform:methanol=10:1) to give Compound c24 (250 mg, 88%) as a white solid by solidifying with ethyl acetate.

(672) .sup.1H-NMR (CDCl.sub.3) 1.19 (d, J=6.7 Hz, 3H), 1.49-1.61 (m, 2H), 1.63-1.72 (m, 2H), 1.94-2.05 (m, 5H), 2.14-2.25 (m, 2H), 3.36-3.50 (m, 3H), 3.70 (d, J=0.9 Hz, 3H), 4.09-4.28 (m, 3H), 5.17-5.23 (m, 1H), 5.66 (d, J=7.0 Hz, 1H), 6.09 (tt, J=55.1, 4.1 Hz, 1H), 6.61 (dd, J=10.7, 6.1 Hz, 1H).

(673) Step 5 Preparation of Compound c25

(674) ##STR00113##

(675) N-bromosuccinimide (106 mg, 0.596 mmol) was added to the acetonitrile (0.5 ml) solution of Compound c24 (250 mg, 0.541 mmol), and the mixture was stirred for 2 hours at 45 C. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (chloroform:methanol=10:1) to give compound c25 (299 mg, quant) as a white solid.

(676) .sup.1H-NMR (CDCl.sub.3) : 1.19 (d, J=6.8 Hz, 3H), 1.51-1.61 (m, 2H), 1.63-1.72 (m, 2H), 1.95-2.04 (m, 5H), 2.15-2.24 (m, 2H), 3.38-3.49 (m, 3H), 3.71 (d, J=0.8 Hz, 3H), 4.10-4.20 (m, 1H), 4.26 (td, J=13.1, 4.2 Hz, 2H), 5.18-5.24 (m, 1H), 5.65 (d, J=7.7 Hz, 1H), 6.17 (tt, J=55.1, 4.2 Hz, 1H).

(677) Step 6 Preparation of Compound c26

(678) ##STR00114##

(679) Trimethylboroxine (0.019 ml, 0.139 mmol), PdCl.sub.2 (dppf) CH.sub.2Cl.sub.2 complex (3.78 mg, 0.00463 mmol), and 2 mol/L aqueous solution of potassium carbonate (0.116 ml, 0.231 mmol) were sequentially added to the 1,4-dioxane (0.5 ml) of solution Compound c25 (50 mg, 0.093 mmol), and the mixture was stirred for 30 minutes at 130 C. under microwave irradiation. Distilled water (10 ml) was added to the reaction mixture, and the mixture was extracted twice with ethyl acetate (10 ml). The organic layer was washed with diluted water (10 ml) and saturated brine (10 ml) each once. The organic layer was dried over sodium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by reverse phase chromatography (H.sub.2O-acetonitrile) to give the compound c26 (25 mg, 57%) as a white solid.

(680) .sup.1H-NMR (CDCl.sub.3) : 1.19 (d, J=6.8 Hz, 3H), 1.49-1.61 (m, 2H), 1.61-1.72 (m, 2H), 1.95-2.04 (m, 5H), 2.15-2.24 (m, 2H), 2.27 (d, J=2.3 Hz, 3H), 3.37-3.49 (m, 3H), 3.68 (d, J=0.8 Hz, 3H), 4.09-4.26 (m, 3H), 5.18-5.24 (m, 1H), 5.66 (d, J=7.3 Hz, 1H), 6.09 (tt, J=55.1, 4.1 H).

Example 18

Preparation of Compound c34

(681) ##STR00115##
Step 1 Preparation of Compound c28

(682) Compounds c27 (18.9 g, 46 mmol) was dissolved in a mixed solution THF (100 mL) and methanol (20 mL), and sodium borohydride (5.2 g, 138 mmol) was added, and the mixture was stirred at room temperature for 15 hours. The aqueous hydrochloric acid was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, the obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give compound c28 (8.7 g, 51% yield).

(683) .sup.1H-NMR (CDCl.sub.3) : 0.71-0.92 (m, 3H), 1.05 (s, 9H), 1.17-1.48 (m, 4H), 1.64-1.74 (m, 2H), 1.81-1.91 (m, 2H), 3.34-3.40 (m, 2H), 3.55 (tt, J=10.8, 5.3 Hz, 1H), 7.32-7.45 (m, 6H), 7.62-7.72 (m, 4H).

(684) Step 2 Preparation of Compound c29

(685) Compounds of c28 (5 g, 13.6 mmol) was dissolved in dichloromethane (50 mL) and Des Martin reagent (7.5 g, 17.6 mmol) was added, and stirred for 3 h at 0 C. Sodium hydrogen sulfite and a saturated sodium bicarbonate solution were added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with water, washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure to obtain a residue containing the aldehyde.

(686) Sodium hydride (678 mg, 17 mmol) was dissolved in THF (50 mL) and ethyl diethylphosphonoacetate (3.5 mL, 17.6 mmol) was added under ice-cooling, and the mixture was stirred for 30 minutes. The residue obtained above was dissolved in THF (10 mL), it was added to the reaction mixture under ice-cooling. The reaction solution was stirred for 1 hour at 0 C. Saturated aqueous ammonium chloride solution was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give compound c29 (4.2 g, 71% yield).

(687) .sup.1H-NMR (CDCl.sub.3) : 0.95-1.07 (m, 2H), 1.05 (s, 9H), 1.26 (t, J=6.5 Hz, 3H), 1.35-1.49 (m, 2H), 1.67-1.76 (m, 2H), 1.81-1.90 (m, 2H), 1.99-2.13 (m, 1H), 3.57 (tt, J=10.5, 4.5 Hz, 1H), 4.15 (q, J=6.5 Hz, 2H), 5.71 (d, J=15.8 Hz, 1H), 6.81 (dd, J=15.8, 7.0 Hz, 1H), 7.31-7.47 (m, 6H), 7.62-7.71 (m, 4H).

(688) Step 3 Preparation of Compound c30

(689) Compound c29 (2.95 g, 6.76 mmol) was dissolved in THF (20 mL) and methanol (3 mL) and sodium borohydride (1.3 g, 33.8 mmol) was added, and the mixture was stirred at room temperature for 4 hours. The aqueous hydrochloric acid was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated brine, and then dried with anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give compound c30 (2.0 g, 76% yield).

(690) .sup.1H-NMR (CDCl.sub.3) : 0.67-0.81 (m, 2H), 1.04 (s, 9H), 1.10-1.20 (m, 3H), 1.30-1.42 (m, 2H), 1.47-1.54 (m, 2H), 1.61-1.68 (m, 2H), 1.78-1.84 (m, 2H), 3.50-3.61 (m, 3H), 7.33-7.44 (m, 6H), 7.65-7.69 (m, 4H).

(691) Step 4 Preparation of Compound c31

(692) Compound c30 (1.43 g, 3.61 mmol) was dissolved in dichloromethane (4 mL) and des Martin reagent (3.1 g, 7.2 mmol) was added, and the mixture was stirred at room temperature for 2 hours. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with a saturated sodium bicarbonate solution and water, and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure to obtain a residue containing the aldehyde.

(693) The residue was dissolved in toluene (4 mL), (R)-tertiary butyl sulfinamide (524 mg, 4.3 mmol) and titanium tetraethoxide (1.07 g, 4.7 mmol) were added, and the mixture was stirred for 1 hour at 80 C. After cooling, water was added to the reaction solution. The precipitated solid was filtered off, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give compound c31 (620 mg, 35% yield).

(694) .sup.1H-NMR (CDCl.sub.3) : 0.77 (q, J=12.5 Hz, 2H), 1.04 (s, 9H), 1.18 (s, 9H), 1.34 (q, J=12.5 Hz, 2H), 1.38-1.48 (m, 2H), 1.54-1.61 (m, 1H), 1.63-1.70 (m, 2H), 1.78-1.86 (m, 2H), 2.46 (td, J=7.5, 5.0 Hz, 2H), 3.55 (tt, J=10.5, 5.0 Hz, 1H), 7.33-7.45 (m, 6H), 7.64-7.70 (m, 4H), 8.01 (t, J=5.0 Hz, 1H).

(695) Step 5 Preparation of Compound c32

(696) Compounds c31 (570 mg, 1.15 mmol) was dissolved in toluene (20 mL), methyl magnesium bromide (3 mol/L diethyl ether solution, 1.5 mL, 4.6 mmol) was added and the mixture was stirred at room temperature. Saturated aqueous ammonium chloride solution was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, the obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give compound c32 (396 mg, 67% yield).

(697) .sup.1H-NMR (CDCl.sub.3) : 0.73-0.76 (m, 2H), 1.04 (s, 9H), 1.08-1.17 (m, 3H), 1.18 (s, 9H), 1.21 (d, J=6.6 Hz, 3H), 1.27-1.39 (m, 3H), 1.39-1.49 (m, 1H), 1.58-1.65 (m, 2H), 1.77-1.84 (m, 2H), 2.82 (d, J=6.7 Hz, 1H), 3.21-3.30 (m, 1H), 3.54 (tt, J=10.4, 5.0 Hz, 1H), 7.33-7.44 (m, 6H), 7.64-7.70 (m, 4H).

(698) Step 6 Preparation of Compound c33

(699) Compound c32 (160 mg, 0.31 mmol) was dissolved in 1,4-dioxane (10 mL) and hydrochloric acid (4 mol/L 1,4-dioxane solution, 0.39 mL, 1.6 mmol) was added, the mixture was stirred at room temperature for 14 hours. The reaction mixture was distilled off under reduced pressure to obtain a residue.

(700) The obtained residue was dissolved in dichloromethane (10 mL), triethylamine (0.43 mL, 3.11 mmol) and acetic anhydride (0.06 mL, 0.62 mmol) were added and the mixture was stirred at room temperature. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, the obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give compound c33 (125 mg, 89% yield).

(701) .sup.1H-NMR (CDCl.sub.3) : 0.72 (q, J=10.7 Hz, 2H), 1.04 (s, 9H), 1.07 (d, J=6.7 Hz, 3H), 1.08-1.20 (m, 3H), 1.23-1.40 (m, 4H), 1.58-1.65 (m, 2H), 1.76-1.83 (m, 2H), 1.93 (s, 3H), 3.53 (tt, J=10.8, 5.6 Hz, 1H), 3.81-3.95 (m, 1H), 5.12 (d, J=7.3 Hz, 1H), 7.33-7.44 (m, 6H), 7.64-7.69 (m, 4H).

(702) Step 7 Preparation of Compound c34

(703) Compound c33 (168 mg, 0.37) was dissolved in THF (10 mL) and tetrabutylammonium fluoride (1 mol/L THF solution, 0.74 mL, 0.74 mmol) was added. After the reaction mixture was stirred at 50 C. for 4 hours, and then evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatograph (chloroform-methanol) to give Compound c34 (75 mg, 95% yield).

(704) .sup.1H-NMR (CDCl.sub.3) : 0.90-1.00 (m, 2H), 1.11 (d, J=6.7 Hz, 3H), 1.13-1.31 (m, 5H), 1.34-1.49 (m, 2H), 1.70-1.82 (m, 2H), 1.89-2.02 (m, 5H), 3.54 (tt, J=10.9, 4.3 Hz, 1H), 3.87-4.00 (m, 1H), 5.18 (d, J=6.4 Hz, 1H).

Example 19

Preparation of Compound c43

(705) ##STR00116##
Step 1 Preparation of Compound c37

(706) The DMF (13.5 ml) solution of Compound c35 (1.35 g, 6.55 mmol) was cooled with ice bath, sodium hydride (0.315 g, 7.87 mmol) was added thereto, and the mixture was stirred at same temperature for 30 minutes. Compound c36 (2.65 g, 7.21 mmol) was added thereto, and the reaction mixture was stirred at room temperature for 1 hour. Additionally, Compound c36 (0.482 g, 1.31 mmol) was added thereto, and the reaction mixture was stirred at 60 C. for 1 hour. After cooled to room temperature, 2 mol/L hydrochloric acid (13.1 mL, 26.2 mmol) was added thereto, and the reaction mixture was stirred at room temperature for 1 hour. The reaction mixture was neutralized with sodium carbonate, and then extracted with ethyl acetate. The organic layer was washed with water, and the solvent was concentrated under reduced pressure. The obtained residue was purified by silica gel chromatography (hexane-ethyl acetate) to afford Compound c37 (1.06 g, yield 33%).

(707) [M+H]=494.20, Method Condition 3: retention time 3.35 min

(708) Step 2 Preparation of Compound c38

(709) Compound c37 (400 mg, 0.810 mmol) was dissolved in tetrabutylammonium fluoride (1 mol/L, THF solution, 1 mL, 1.00 mmol). The reaction mixture was stirred at room temperature for 16 hours. The reaction solution was evaporated under reduced pressure, and the obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to afford Compound c38 (272 mg, yield 89%).

(710) [M+H]=380.15, Method Condition 3: retention time 2.29 min

(711) Step 3 Preparation of a Mixture of Compound c39 and c40

(712) The dichloromethane solution of imidazole (293 mg, 4.30 mmol) was cooled with ice bath, and thionyl chloride (0.094 mL, 1.29 mmol) was added thereto at room temperature for 1 hour. The reaction mixture was cooled to 15 C., and the dichloromethane (8 ml) solution of Compound c38 (272 mg, 0.717 mmol) was added thereto dropwise. The reaction mixture was stirred at room temperature for 3 hours. 10% citric acid aqueous solution was added to the reaction mixture, and the reaction mixture was extracted. The organic layer was washed with water, and the solvent was concentrated under reduced pressure. The obtained residue was dissolved in dichloromethane (4 mL), sodium meta-periodate (399 mg, 1.86 mol) and ruthenium oxide hydrate (2.4 mg, 0.016 mmol) were added thereto. The reaction mixture was stirred at room temperature for 2 hours. The reaction mixture was diluted with ethyl acetate, and the insoluble matter was filtered off. The filtrate was extracted, and the organic layer was washed with water, and then the solvent was concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to afford a mixture of Compound c39 (148 mg, yield 47%) and Compound c40 (84 mg, yield 26%). Wherein, the ratio of both was calculated based on the area ratio (1.00:0.55) of completely independent two signals at 4.26 ppm (2H, s, Compound c39) and 5.00-5.10 ppm (1H, m, Compound c40) in .sup.1H-NMR.

(713) Step 4 Preparation of a Mixture of Compound c41 and c42

(714) The mixture of Compound c39 (141 mg, 0.320 mmol) and Compound c40 (80 mg, 0.176 mmol) was dissolved in tetrabutylammonium fluoride (1 mol/L, THF solution, 0.991 mL, 0.991 mmol), and stirred at room temperature for 21 hours. 10% citric acid aqueous solution (2 mL) was added to the reaction mixture, and the reaction mixture was stirred at room temperature for 1 hour. The reaction mixture was extracted with ethyl acetate, and the organic layer was concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to afford a mixture of Compound c41 (110 mg, yield 90%) and Compound c42 (63 mg, yield 90%). Wherein, the ration of both was calculated based on the area ratio (1.00:0.55) of completely independent two signals at 4.78-4.92 ppm (1H, m, Compound c41) and 5.00-5.10 ppm (1H, m, Compound c42) in .sup.1H-NMR.

(715) Step 5 Preparation of Compound c43

(716) The mixture of Compound c41 (108 mg, 0.283 mmol) and Compound c42 (62 mg, 0.156 mmol) was dissolved in ethyl acetate (5 mL). 10% palladium-carbon catalyst (wetted with 50% water, 56 mg, 0.013 mmol) was added to the reaction mixture, and the reaction mixture was stirred under hydrogen atmosphere at room temperature for 24 hours. The reaction mixture was filtered, and the filtrate was concentrated under reduced pressure. The obtained crude product of a mixture of Compound a43 and unreacted Compound a42 was dissolved in THF (2 mL) and methanol (2 mL). 2 mol/L sodium hydrate aqueous solution (0.283 mL, 0.566 mmol) was added to the reaction mixture, and the reaction mixture was stirred at room temperature for 4.5 hours. The reaction mixture was concentrated, and extracted with ethyl acetate. After concentrated under reduced pressure, the obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to afford Compound a43 (121 mg, yield 95%).

(717) .sup.1H-NMR (CDCl.sub.3) : 1.29-1.38 (4H, m), 1.45 (9H, s), 1.91-2.03 (4H, m), 3.27-3.33 (1H, m), 3.48 (1H, ddd, J=9.4, 6.0, 1.8 Hz), 3.59 (1H, ddd, J=9.4, 4.0, 1.3 Hz), 3.67-3.73 (1H, m), 3.88-3.97 (1H, m), 4.40 (1H, ddd, J=47.4, 9.0, 6.0 Hz), 4.39-4.60 (1H, m), 4.82-4.88 (1H, m).

Example 6

Preparation of Compound c45

(718) ##STR00117##
Step 1 Preparation of Compound c45

(719) Compound c44 (17 mg, 0.073 mmol) was dissolved in THF (510 ul), tert-butoxypotassium (20.4 mg, 0.182 mmol) and Compound c43 (35.7 mg, 0.109 mmol) were added to the mixture under ice-cooling, and the mixture was stirred for 2 hours. Saturated aqueous ammonium chloride solution was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with brine and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the obtained residue was purified by silica gel column chromatography (chloroform-methanol) to give the compound c45 (11.9 mg, 0.025 mmol, 34.1%).

(720) .sup.1H-NMR (CDCl.sub.3) : 1.57 (2H, m), 1.70 (4H, m), 2.01 (2H, m), 2.03 (3H, s), 2.19 (2H, m), 3.54 (3H, m), 3.70 (3H, s), 4.60-4.19 (5H, m), 5.20 (1H, m), 5.80 (1H, s), 5.80 (1H, s), 6.61 (1H, dd, J=10.6, 6.1 Hz).

(721) [M+Na]=502.2, Method Condition 2: retention time 2.01 minutes

Example 21

Preparation of Compound c56

(722) ##STR00118##
Step 1 Preparation of Compound c47

(723) Compound c46 (11.6 g, 66.4 mmol; J. Org. Chem. 1998, 63, 8133-8144) was dissolved in dichloromethane (116 mL). Tert-buthyldiphenylsilylchoride (20.5 ml, 80 mmol) and imidazole (6.8 g, 100 mmol) were added to the mixture, and the mixture was stirred at room temperature. Water was added to the mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with 1 mol/L hydrochloric acid and saturated brine, and dried over anhydrous sodium sulfate. The solvent was condensed under reduced pressure to afford a crude product. The afforded crude product was dissolved in THF (116 mL) and methanol (58 mL), and 2 mol/L aqueous sodium hydroxide (100 mL) was added to the mixture. The mixture was stirred at room temperature for two hours. Water was added to the mixture, and the mixture was extracted with ethyl acetate. The organic layer was dried over saturated brine and dried over anhydrous sodium sulfate. The obtained residue was purified by silica gel chromatography (hexane-ethyl acetate) to afford Compound a47 (17.3 g, yield 70%).

(724) .sup.1H-NMR (CDCl.sub.3) : 1.06 (s, 9H), 1.56 (m, 1H), 1.64-1.73 (m, 2H), 1.94 (m, 1H), 2.14 (d, J=8.4 Hz, 1H), 3.45 (m, 1H), 3.57 (d, J=12.0 Hz, 1H), 3.59 (dd, J=5.6, 10.4 Hz, 1H), 3.72 (dd, J=5.6, 10.8 Hz, 1H), 3.75 (m, 1H), 3.85 (ddd, J=2.4, 2.4, 12.0 Hz, 1H), 7.44-7.35 (m, 6H), 7.69-7.65 (m, 4H).

(725) Step 2 Preparation of Compound c48

(726) Oxalyl chloride (2.5 g, 16 mmol) was dissolved in dichloromethane (100 mL), dimethyl sulfoxide (5.4 ml, 76 mmol) was added to the mixture under 78 C. and the mixture was stirred for 1 hour. Methylene chloride solution (20 mL) of Compound c47 (7.0 g, 18.9 mmol) was added to the mixture, then the mixture was stirred 2 hours. Triethylamine (21 ml, 151 mmol) was added to the reaction solution, and the mixture was stirred at room temperature for 1 hour. The saturated sodium bicarbonate water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated brine, and then dried over anhydrous sodium sulfate. The obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to afford the aldehyde (13.1 g, 94% yield).

(727) .sup.1H-NMR (CDCl.sub.3) : 1.07 (s, 9H), 1.95 (m, 1H), 2.10 (m, 1H), 2.47 (ddd, J=6.8, 10.8, 16.8 Hz, 1H), 2.60 (ddd, J=4.8, 4.8, 16.8 Hz, 1H), 3.69 (m, 1H), 3.79 (m, 1H), 3.81 (m, 1H), 3.94 (d, J=16.8 Hz, 1H), 4.14 (d, J=16.8 Hz, 1H), 7.46-7.36 (m, 6H), 7.69-7.66 (m, 4H).

(728) Step 3 Preparation of Compound c49

(729) Compound c48 (8.0 g, 21.7 mmol) was dissolved in diethyl ether (240 mL), lithium aluminum hydride (0.99 g, 26 mmol) was added, and the mixture was stirred at 0 C. for 0.5 hour. Water (2.97 mL) and 2 mol/L sodium hydroxide (0.99 mL) were added to the reaction solution, and the mixture was stirred at room temperature for 1 hour. An anhydrous sodium sulfate (30 g) was added to the reaction solution and the mixture was filtered. The obtained filtrate was distilled off under reduced pressure, silica gel column chromatography (hexane-ethyl acetate) to give compound c49 (8.0 g, 99.5% yield).

(730) .sup.1H-NMR (CDCl.sub.3) : 1.05 (s, 9H), 1.36-1.42 (m, 2H), 1.83 (m, 1H), 2.13 (m, 1H) 3.09 (dd, J=10.4, 10.4 Hz, 1H), 3.36 (m, 1H), 3.57 (dd, J=5.6, 10.4 Hz, 1H), 3.68 (m, 1H), 3.72 (dd, J=5.6, 10.4 Hz, 1H), 4.00 (ddd, J=2.0, 4.8, 10.4 Hz, 1H), 7.44-7.35 (m, 6H), 7.69-7.64 (m, 4H).

(731) Step 4 Preparation of Compound c50

(732) The compound c49 (12.5 g, 33.7 mmol) was dissolved in DMF (125 mL), benzyl bromide (4.81 ml, 40.5 mmol) and sodium hydride (2.0 g, 50.6 mmol) was added to the mixture at 0 C., and the mixture was stirred at room temperature for 2 hours. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with hydrochloric acid and saturated brine, and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure to give the crude product.

(733) The obtained crude product was dissolved in THF (125 mL), 1 mol/L tetrabutylammonium fluoride (50.6 mL, 50.6 mmol) was added, and the mixture was stirred for 1 hour. The reaction solution was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give Compound c50 (6.84 g, 88% yield) and its isomer (0.32 g, yield: 4.1%).

(734) .sup.1H-NMR (CDCl.sub.3) 6:1.32-1.53 (m, 2H), 1.64 (m, 1H), 2.23 (m, 1H) 3.22 (dd, J=10.4, 10.4 Hz, 1H), 3.36-3.52 (m, 3H), 3.60 (d, J=11.2 Hz, 1H), 4.11 (ddd, J=2.0, 4.4, 10.8 Hz, 1H), 4.54 (d, J=11.6 Hz, 1H), 4.60 (d, J=11.6 Hz, 1H), 7.37-7.27 (m, 5H).

(735) Step 5 Preparation of Compound c51

(736) Compound c50 (500 mg, 2.25 mmol) was dissolved in methylene chloride (10 mL) and Des Martin reagent (1.43 g, 3.37 mmol) was added under ice-cooling. The reaction mixture was stirred at room temperature for 1 hour. The saturated sodium bicarbonate water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and then dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and the obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to afford the aldehyde (1.3 g, 67% yield).

(737) To THF solution of methyl triphenylphosphonium bromide (3.18 g, 7.87 mmol), tert-butoxy potassium (757 mg, 6.75 mmol) was added at 78 C., and the mixture was stirred at room temperature for 2 hours. THF solution of the aldehyde (3 mL) was added under 78 C., and the mixture was stirred at room temperature overnight. A saturated aqueous ammonium chloride was added to the mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated brine, and then dried over anhydrous sodium sulfate. The obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give compound c51 (0.47 g, 96% yield).

(738) .sup.1H-NMR (CDCl.sub.3) : 1.37-1.54 (m, 2H), 1.81 (m, 1H), 2.22 (m, 1H) 3.22 (dd, J=10.4, 10.4 Hz, 1H), 3.48 (m, 1H), 3.77 (dd, J=3.6, 9.2 Hz, 1H), 4.14 (m, 1H), 4.54 (d, J=12.0 Hz, 1H), 4.60 (d, J=12.0 Hz, 1H), 5.10 (d, J=10.8 Hz, 1H), 5.24 (d, J=17.6 Hz, 1H), 5.82 (dd, J=5.6, 10.4, 17.6 Hz, 1H), 7.37-7.27 (m, 5H).

(739) Step 6 Preparation of Compound c52

(740) To dichloromethane (5.3 mL) solution of Compound c51 (0.47 g, 2.15 mmol), (S)-2-(3-buten-2-yl) isoindoline-1,3-dione (886 mg, 4.31 mmol) and Grubbs II reagent (55 mg, 0.065 mmol) was added, and the mixture was stirred at 40 C. overnight. The reaction solution was distilled off under reduced pressure, the obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give compound c52 (0.45 g, 53% yield).

(741) [M+H]=392.3, Method Condition 4: retention time 2.52 minutes

(742) Step 7 Preparation of Compound c53

(743) Compound c52 (445 mg, 1.14 mmol) was dissolved in ethanol (4.5 mL), hydrazine (109 mg, 3.41 mmol) was added, and the mixture was stirred at 40 C. for 5 hours. Water was added to the reaction mixture, and the mixture was extracted with dichloromethane. The organic layer was washed with saturated brine, and then dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the resulting residue was dissolved in methylene chloride (4.5 mL). Boc .sub.2O (396 l, 1.71 mmol) and triethylamine (315 l, 2.27 mmol) was added, and the mixture was stirred at room temperature overnight. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and then dried over anhydrous sodium sulfate. The obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give compound c53 (397 mg, 97% yield).

(744) .sup.1H-NMR (CDCl.sub.3) : 1.19 (d, J=8.0 Hz, 3H), 1.37-1.54 (m, 2H), 1.43 (s, 9H), 1.78 (m, 1H), 2.20 (m, 1H) 3.23 (m, 1H), 3.46 (m, 1H), 3.77 (m, 1H), 4.12 (m, 1H), 4.51-4.61 (m, 3H), 5.10 (dd, J=5.6, 15.6 Hz, 1H), 5.67 (m, 1H), 7.37-7.27 (m, 5H).

(745) [M+H]=362.3, Method Condition 4: retention time 2.51 minutes

(746) Step 8 Preparation of Compound c54

(747) Compound c53 (395 mg, 1.095 mmol) was dissolved in a mixed solution of methanol (8 ml) and ethyl acetate (4 ml), palladium hydroxide (40 mg) was added, and the mixture was stirred for 2 hours under a hydrogen atmosphere. The reaction mixture was filtered, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (chloroform-methanol) to give Compound c54 (160 mg, 54% yield).

(748) .sup.1H-NMR (CDCl.sub.3) : 1.11 (d, J=6.8 Hz, 3H), 1.32-1.54 (m, 6H), 1.43 (s, 9H), 1.70 (m, 1H), 2.11 (m, 1H) 3.09 (dd, J=10.8, 10.8 Hz, 1H), 3.21 (m, 1H), 3.68 (m, 2H), 4.00 (m, 1H), 4.33 (m, 1H).

(749) [M+H]=274.3, Method Condition 4: retention time 1.46 minutes

(750) Step 9 Preparation of Compound c55

(751) Compound c18 (41 mg, 0.121 mmol) and the compound c54 (30 mg, 0.110 mmol) were dissolved in THF (0.5 mL), tert-butoxy potassium (31 mg, 0.274 mmol) was added and the mixture was stirred for 1 hour at 0 C. A saturated aqueous ammonium chloride was added to the mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and then dried with anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and the resulting residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give compound c55 (45 mg, 77% yield).

(752) [M+H]=536.4, Method Condition 4: retention time 1.98 minutes

(753) Step 10 Preparation of Compound c56

(754) Compound c55 (27 mg, 0.062 mmol) was dissolved in dichloromethane (0.5 mL) and trifluoroacetic acid (0.05 ml, 0.62 mmol) was added at 0 C., and the mixture was stirred at room temperature for 4 hours. The reaction mixture was evaporated under reduced pressure. The obtained residue was dissolved in THF (0.5 mL), and trichloroacetyl isocyanate (23 mg, 0.124 mmol) and triethylamine (0.034 ml, 0.248 mmol) was added at 0 C. The reaction mixture was stirred for 1 hour at room temperature. The reaction mixture was concentrated under reduced pressure, and the residue was dissolved in methanol (1 ml). Potassium carbonate (34 mg, 0.248 mmol) was added to the reaction mixture and the mixture was stirred for 2 hours. Water was added to the reaction mixture, and the mixture was extracted with dichloromethane. The organic layer was washed with saturated brine, and then dried with anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, the resulting residue was purified by silica gel column chromatography (chloroform-methanol) to give Compound c56 (14 mg, 47% yield).

(755) .sup.1H-NMR (CDCl.sub.3CD.sub.3OD) : 1.14 (d, J=6.4 Hz, 3H), 1.37-1.54 (m, 4H), 1.68 (m, 1H), 1.89-1.80 (m, 2H), 2.40 (m, 1H), 3.30-3.42 (m, 2H), 3.78-3.68 (m, 2H), 3.84 (s, 3H), 4.22 (dt, J=4.0, 13.2 Hz, 1H), 4.28 (m, 1H), 5.10 (m, 1H), 5.18 (d, J=7.6 Hz, 1H), 6.13 (tt, J=4.0, 54.8 Hz, 1H), 6.66 (d, J=10.8 Hz, 1H).

(756) [M+H]=479.3, Method Condition 4: retention time 1.98 minutes

Example 22

Preparation of Compound c62

(757) ##STR00119##
Step 1 Preparation of Compound a58

(758) Compound c57 (131 mg, 0.54 mmol; WO201005562) was dissolved in dichloromethane (2.5 mL), and 1 mol/L diisobutylalminium hydride (2.16 ml, 2.16 mmol) were added thereto at 78 C. It was stirred at room temperature for 1 hour. Ethyl acetate (0.4 ml), saturated Rochelle's salt and ethyl acetate (5 ml) were added the reaction mixture, and the mixture was stirred for 1 hour at room temperature. The reaction mixture was concentrated under reduced pressure, and extracted with dichloromethane. The organic layer was washed with water and brine, and then dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, the resulting residue was purified by silica gel column chromatography (chloroform-methanol) to afford Compound a58 (63 mg, 58% yield).

(759) .sup.1H NMR (CDCl.sub.3) : 1.28 (t, J=7.2 Hz, 3H), 1.29 (d, J=7.2 Hz, 3H), 2.01 (s, 3H), 4.17 (q, J=7.2 Hz, 2H), 4.74 (m, 1H), 5.42 (br.s, 1H), 5.89 (d, J=15.6 Hz, 1H), 6.87 (dd, J=4.8, 15.6 Hz, 1H).

(760) Step 2 Preparation of Compound c59

(761) Compounds a58 (440 mg, 2.04 mmol) was dissolved in dichloromethane (4 mL), and trifluoroacetic acid (1.57 ml, 20.4 mmol) was added at 0 C. The mixture was stirred for 30 minutes. The reaction mixture was concentrated under reduced pressure, and triethylamine (847 l, 6.11 mmol) and acetic anhydride (385 l, 4.07 mmol) were added to the dichloromethane solution of the resulting residue (3.0 mL). The reaction mixture was stirred for 1 hour. To the reaction mixture was added water and extracted with dichloromethane. The organic layer was washed with 2 mol/L hydrochloric acid and saturated brine, and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, the resulting residue was dissolved in THF-H.sub.2O (2 ml; 1:1), and 2 mol/L sodium hydroxide was added thereto. The reaction solution was stirred at room temperature for 30 minutes. Water was added to the reaction mixture, and the mixture was extracted with dichloromethane. The organic layer was washed with water and brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (chloroform-methanol) to afford Compound c59 (220 mg, 75% yield).

(762) .sup.1H NMR (CDCl.sub.3) : 1.25 (d, J=6.8 Hz, 3H), 1.40 (s, 1H), 1.99 (s, 3H), 4.55 (br.s, 2H), 4.60 (m, 1H), 5.32 (s, 1H), 5.68 (m, 1H), 5.76 (m, 1H).

(763) Step 3 Preparation of Compound c60

(764) Compounds c59 (40 mg, 0.279 mmol) was dissolved in dichloromethane (2 mL) and manganese dioxide (484 mg, 5.56 mmol) was added thereto, and it was stirred for 1 hour. The reaction mixture was filtered, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give the aldehyde compound (28 mg, 71% yield).

(765) 2-(benzyloxy) propane-1,3-diol (54 mg, 0.298 mmol) and pyridinium paratoluene sulfonate (2.5 mg, 9.9 mol) were added to the toluene (1 ml) solution of the aldehyde, and it was stirred at 90 C. for 6 hours. The reaction solution was concentrated, and the residue was purified by prep HPLC (0.1% formic acid-containing acetonitrile-water) to afford Compound c60 (3.8 mg, 6% yield) and its cis isomer (4.0 mg, 6% yield).

(766) .sup.1H NMR (CDCl.sub.3) : 1.23 (d, J=8.4 Hz, 3H), 1.95 (s, 3H), 3.49 (dd, J=10.8, 10.8 Hz, 2H), 3.67 (m, 1H), 3.49 (dd, J=4.8, 10.8 Hz, 2H), 4.56 (s, 2H), 4.62 (m, 1H), 4.86 (d, J=4.4 Hz, 1H), 5.32 (d, J=8.4 Hz, 1H), 5.59 (ddd, J=1.6, 4.4, 15.6 Hz, 1H) 5.93 (dd, J=5.2, 15.6 Hz, 1H), 7.27-7.37 (m, 5H).

(767) Cis isomer; .sup.1H NMR (CDCl.sub.3) : 1.24 (d, J=6.8 Hz, 3H), 1.96 (s, 3H), 3.25 (s, 1H), 3.87 (d, J=12.0 Hz, 2H), 4.23 (d, J=12.0 Hz, 2H), 4.64 (m, 1H), 4.67 (s, 2H), 5.02 (d, J=4.8 Hz, 1H), 5.36 (d, J=7.2 Hz, 1H), 5.69 (ddd, J=1.6, 4.4, 16.0 Hz, 1H) 5.98 (dd, J=4.8, 16.0 Hz, 1H), 7.27-7.39 (m, 5H).

(768) Step 4 Preparation of Compound c61

(769) Compound c60 (4.0 mg, 0.012 mmol) was dissolved in methanol (1 mL), and palladium hydroxide (1 mg, 0.16 mmol) was added thereto. The reaction mixture was stirred under hydrogen atmosphere for 5 hours. The reaction solution was filtered, and the filtrate was concentrated under reduced pressure to afford Compound c61 (2.6 mg, 100% yield) as a crude product.

(770) .sup.1H NMR (CDCl.sub.3) : 1.13 (d, J=6.8 Hz, 3H), 1.45-1.68 (m, 4H), 1.95 (s, 3H), 3.67 (dd, J=10.8, 10.8 Hz, 2H), 3.67 (m, 1H), 3.88 (m, 1H), 3.97 (m, 1H), 4.16 (dd, J=4.8, 10.8 Hz, 2H), 4.44 (dd, J=4.8, 4.8 Hz, 1H), 5.31 (br.s, 1H).

(771) Step 5 Preparation of Compound c62

(772) Compound c22 (7.5 mg, 0.023 mmol) and Compound c61 (2.6 mg, 0.012 mmol) was dissolved in THF (0.5 mL) and, tert-butoxy potassium (3.2 mg, 0.029 mmol) was added, and the mixture was stirred for 1 hour at 0 C. A saturated aqueous ammonium chloride was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and then dried with anhydrous sodium sulfate. The solvent was distilled off under reduced pressure. The resulting residue was purified bywas purified by (0.1% formic acid-containing acetonitrile-water) with preparative HPLC to give Compound c62 (2.3 mg, 43% yield).

(773) .sup.1H-NMR (CDCl.sub.3) 1.14 (d, J=6.4 Hz, 3H), 1.37-1.54 (m, 4H), 1.96 (s, 3H), 3.62 (dd, J=10.4, 10.4 Hz, 2H), 3.68 (s, 2H), 3.99 (m, 1H), 4.22 (dt, J=4.0, 13.2 Hz, 2H), 4.51 (dd, J=5.6, 11.2 Hz, 2H), 4.57 (dd, J=4.4, 4.4 Hz, 1H), 6.13 (tt, J=4.0, 54.8 Hz, 1H), 6.63 (d, J=6.0, 10.8 Hz, 1H).

(774) [M+H]=0.4, Method Condition 4: retention time 1.87 minutes

Example 23

Preparation of Compound c66

(775) ##STR00120##
Step 1 Preparation of Compound c64

(776) Compound c63 (3.0 g, 127 mmol) was dissolved in a mixed solution of DMF (30 mL) and THF (30 mL) and sodium hydride (0.51 g, 12.7 mmol) was added under ice-cooling. The reaction mixture was stirred for 30 minutes under ice-cooling. The THF solution (5 mL) of (S)-3-benzyl-4-methyl-1,2,3-oxathiazolidine-2,2-dioxide (2.31 g, 10.15 mmol) was added to the reaction mixture under ice-cooling, and the mixture was stirred for 2 hours at 40 C. 2 mol/L aqueous hydrochloric acid solution (17 mL) was added to the reaction solution under ice-cooling, and the reaction mixture was stirred for 1 hour at room temperature. In addition 2 mol/L sodium hydroxide solution (30 mL) was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The reaction solvent was distilled off under reduced pressure, and the resulting residue was purified by amino silica gel column chromatographywas purified by (chloroform-methanol) to give Compound c64 (3.7 g, 87% yield).

(777) .sup.1H NMR (CDCl.sub.3) : 1.01 (d, J=6.0 Hz, 3H), 1.05 (m, 9H), 1.15-1.22 (m, 2H), 1.33-1.41 (m, 2H), 1.74 (m, 2H), 1.88 (m, 2H), 2.85 (m, 1H), 3.25 (m, 2H), 3.35 (dd, J=4.0, 9.2 Hz, 1H), 3.68 (m, 1H), 3.70 (d, J=13.2 Hz, 1H), 3.83 (d, J=13.2 Hz, 1H), 7.20-7.44 (m, 11H), 7.66 (d, J=6.8 Hz, 4H).

(778) Step 2 Preparation of Compound c65

(779) Compound c64 (50.5 g, 101 mmol) was dissolved in ethanol (505 mL), and PdC(11.3 g, 5.0 mmol) and ammonium formate (12.7 g, 201 mmol) were added to the mixture. The mixture was stirred at 65 C. for 3 hours. Further ammonium formate (6.35 g, 101 mmol) was added to the mixture, and the mixture was stirred at 65 C. for 2.5 hours. The reaction mixture was filtered, and the filtrate was concentrated under reduced pressure. A saturated aqueous solution of sodium carbonate was added to the residue and the mixture was extracted with ethyl acetate. The organic layer was washed with water and brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the residue dissolved in dichloromethane (253 mL), triethylamine (13.95 ml, 101 mmol) and acetic anhydride (10.5 ml, 111 mmol) was stirred for 1.5 hours at room temperature was added. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with brine and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, the resulting residue was purified by silica gel column chromatographywas purified by (chloroform-methanol) to give Compound c65 (37.75 g, 83% yield).

(780) .sup.1H NMR (CDCl.sub.3) : 1.05 (m, 9H), 1.12 (d, J=6.8 Hz, 3H), 1.16-1.26 (m, 2H), 1.33-1.43 (m, 2H), 1.75 (m, 2H), 1.89 (m, 2H), 1.93 (s, 3H), 3.28 (m, 1H), 3.32 (m, 1H), 3.38 (dd, J=4.0, 9.2 Hz, 1H), 3.71 (m, 1H), 4.08 (m, 1H), 5.63 (m, 1H), 7.34-7.44 (m, 6H), 7.66 (d, J=6.8 Hz, 4H).

(781) Step 3 Preparation of Compound c66

(782) Compound c65 (30.2 g, 66.6 mmol) was dissolved in THF (100 mL) and 1 mol/L tetrabutylammonium fluoride (100 mL, 100 mmol) was added to the mixture. The mixture was stirred at 70 C. for 7 hours. The reaction solution was distilled off under reduced pressure, the residue was purified by silica gel column chromatography (chloroform-methanol) to give Compound c66 (11.65 g, 81% yield).

(783) .sup.1H NMR (CDCl.sub.3) : 1.17 (d, J=6.8 Hz, 3H), 1.23-1.35 (m, 4H), 1.8-1.90 (m, 2H), 1.97 (s, 3H), 3.27 (m, 1H), 3.38 (dd, J=4.0, 9.6 Hz, 1H), 3.44 (dd, J=4.0, 9.6 Hz, 1H), 3.72 (m, 1H), 4.13 (m, 1H), 5.66 (br.s, 1H).

Example 24

Preparation of Compound c69

(784) ##STR00121##
Step 1 Preparation of Compound c68

(785) The compounds of c67 (10 g, 52 mmol) was dissolved in a mixed solution of DMF (100 mL) and THF (50 mL), and sodium hydride (2.5 g, 62.4 mmol) was added to the mixture under ice-cooling. The mixture was stirred for 30 minutes under ice-cooling. THF (40 mL) solution of (S)-3-benzyl-4-methyl-1,2,3-oxathiazolidine-2,2-dioxide (15.4 g, 67.6 mmol) was added to the reaction solution under ice-cooling. The mixture was stirred at room temperature for 2 hours. 2 mol/L hydrochloric acid aqueous solution (100 mL) was added to the reaction solution under ice-cooling, and the mixture was stirred for 1 hour at room temperature. 2 mol/L sodium hydroxide solution (100 mL) was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was distilled off under reduced pressure, the residue was purified by amino silica gel column chromatography (chloroform-methanol) to give Compound c68 (13.4 g, 76% yield).

(786) .sup.1H NMR (CDCl.sub.3) : 1.05 (d, J=6.4 Hz, 3H), 2.07 (m, 4H), 2.91 (m, 1H), 3.19 (dd, J=7.6, 9.2 Hz, 1H), 3.32 (dd, J=4.4, 9.2 Hz, 1H), 3.45 (m, 2H), 3.73 (d, J=12.8 Hz, 1H), 3.86 (d, J=12.8 Hz, 1H), 4.00 (m, 1H), 4.12 (m, 1H), 4.52 (s, 2H), 7.21-7.37 (m, 10H).

(787) Step 2 Preparation of Compound c69

(788) The compound c68 (1.0 g, 101 mmol) was dissolved in methanol (30 mL), and palladium hydroxide (827 mg, 0.589 mmol) and acetic acid (0.34 ml, 5.89 mmol) were added to the mixture. The mixture was stirred overnight under hydrogen atmosphere. The solvent was evaporated under reduced pressure, and the residue was dissolved in methanol (10 mL), and triethylamine (1.22 ml, 8.84 mmol) and acetic anhydride (0.56 ml, 5.89 mmol) were added to the mixture room temperature for 3 hours. The reaction mixture was concentrated under reduced pressure. A saturated aqueous solution of sodium carbonate was added to the residue and extracted with ethyl acetate. The organic layer was washed with water and brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (chloroform-methanol) to give Compound c69 (483 mg, 81.5% yield).

(789) .sup.1H NMR (CDCl.sub.3) : 1.18 (d, J=6.8 Hz, 3H), 1.46 (br.s, 1H), 1.98 (s, 3H), 2.08 (m, 4H), 2.39 (m, 1H), 3.25 (dd, J=4.0, 9.2 Hz, 1H), 3.32 (dd, J=4.0, 9.2 Hz, 1H), 3.64 (m, 2H), 4.04 (m, 1H), 4.12 (m, 1H), 5.70 (br.s, 1H).

Example 25

Preparation of Compound c81

(790) ##STR00122## ##STR00123##
Step 1 Preparation of Compound c71

(791) Compound c70 (1.0 g, 4.15 mmol) was dissolved in dioxane (16 mL), and tertiary butyl methyl carbamate (653 mg, 4.98 mmol), 2-dicyclohexylphosphino-2,4,6-triisopropyl-biphenyl (297 mg, 0.622 mmol), potassium phosphate (2.20 g, 10.73 mmol) and tris (dibenzylideneacetone) palladium (190 mg, 0.207 mmol) were added to the mixture at 100 C. for 5 hours. Tertiary butyl methyl carbamate (218 mg, 1.66 mmol), 2-dicyclohexylphosphino-2,4,6-triisopropyl biphenyl (99 mg, 0.207 mmol), potassium phosphate (0.73 g, 3.57 mmol) and tris (dibenzylideneacetone) palladium (0) (63.3 mg, 0.069 mmol) were added to the mixture and the mixture was stirred for 3 hours. Tertiary butyl methyl carbamate (435 mg, 3.32 mmol), 2-dicyclohexylphosphino-2,4,6-triisopropyl biphenyl (99 mg, 0.207 mmol) and tris (dibenzylideneacetone) palladium (0) (63.3 mg, 0.069 mmol) was then added to the mixture and the mixture was stirred for 5.5 hours. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give compound c71 (0.75 g, 74% yield).

(792) [M+H]=244.95, Method Condition 3: retention time 2.08 min

(793) Step 2 Preparation of Compound c72

(794) Cyclopropanol (105 mg, 1.80 mmol) was dissolved in THF (5.0 mL) and Compound c71 (400 mg, 1.64 mmol) was added to the mixture. Tertiary butoxy potassium (239 mg, 2.12 mmol) was added to the reaction mixture under ice-cooling and the mixture was stirred for 3.5 hours under ice-cooling. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to give compound c72 a (440 mg) as a crude product.

(795) [M+H]=283.30, Method Condition 3: retention time 2.18 min

(796) Step 3 Preparation of Compound c73

(797) Compound c72 (440 mg, 1.55 mmol) was dissolved in dichloromethane (5.0 mL) and 4 mol/L of hydrochloric acid-dioxane (10 mL, 40 mmol) was added to the mixture. Then the mixture was stirred at room temperature for 20 hours. The reaction solution was evaporated under reduced pressure, and 1 mol/L of aqueous sodium carbonate solution was added to the mixture. The mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to give compound c73 a (278 mg) as a crude product.

(798) [M+H]=183.00, Method Condition 3: retention time 0.98 min

(799) Step 4 Preparation of Compound c74

(800) Compound c73 was dissolved in acetonitrile (5.0 mL), and N-bromosuccinimide (312 mg, 1.72 mmol) was added to the mixture. The mixture was stirred for 2 hours at room temperature. After vacuum evaporation of the solvent, the residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give compound c74 (173 mg, 40% yield).

(801) .sup.1H-NMR (CDCl.sub.3) : 0.77-0.82 (m, 4H), 3.17-3.20 (m, 3H), 4.25-4.27 (m, 1H), 4.44 (s, 1H).

(802) [M+H]=262.85, Method Condition 3: retention time 2.09 min

(803) Step 5 Preparation of Compound c75

(804) Compound c74 (173 mg, 0.663 mmol) was dissolved in DMF (3.0 mL) and sodium hydride (34.5 mg, 0.861 mmol) was added to the mixture under ice-cooling, and the mixture was stirred for 5 minutes. Benzyl bromide (0.087 mL, 0.729 mmol) was added to the reaction solution, and the mixture was stirred for 1.5 hours under ice-cooling. Sodium hydride (3.5 mg, 0.086 mmol) and benzyl bromide (0.009 mL, 0.0757 mmol) were added, and the mixture was stirred for 50 minutes. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and the organic layer was dried over anhydrous magnesium sulfate. After vacuum evaporation of the solvent, the residue was purified by silica gel column chromatography-(hexane-ethyl acetate) to give Compound c75 (174 mg, 75% yield).

(805) [M+H]=350.90, Method Condition 3: retention time 2.86 min

(806) Step 6 Preparation of Compound c76

(807) Compound c75 (170 mg, 0.484 mmol) was dissolved in toluene (4.0 mL), tertiary butoxy sodium (93.0 mg, 0.968 mmol), tris (dibenzylideneacetone) palladium (0) (44.3 mg, 0.048 mmol), 2,2-bis (diphenylphosphino)-1,1-binaphthyl (60.3 mg, 0.097 mmol) and benzyl amine (0.212 mL, 1.938 mmol) were added to the mixture and the mixture was stirred at 100 C. for 2 hours. Its salt was removed by filtration, and the reaction solution was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give compound c76 (140 mg, 76% yield).

(808) [M+H]=378.05, Method Condition 3: retention time 2.83 min

(809) Step 7 Preparation of Compound c77

(810) Compound c76 (140 mg, 0.371 mmol) was dissolved in methanol (3.0 mL), palladium-carbon (96.0 mg, 0.115 mmol) and ammonium formate (234 mg, 0.371 mmol) was added to the mixture. The mixture was stirred at 60 C. for 45 minutes. The reaction mixture was cooled to room temperature and dichloromethane (5.0 mL) was added to the mixture The insoluble was removed by Celite filtration. The solvent was evaporated under reduced pressure to give compound c77 the (69.0 mg) as a crude product.

(811) [M+H]=198.00, Method Condition 3: retention time 1.08 min

(812) Step 8 Preparation of Compound c78

(813) Compound c77 (69.0 mg, 0.349 mmol) was dissolved in THF (3.0 mL) and triethylamine (0.206 mL, 1.484 mmol) and 1,1-thiocarbonyldiimidazole (74.2 mg, 0.408 mmol) was added to the mixture. The mixture was stirred at room temperature for 2 hours. Triethylamine (0.100 mL, 0.722 mmol) and 1,1-thiocarbonyldiimidazole (20.0 mg, 0.112 mmol) was added to the mixture, and the mixture was stirred at room temperature for 1 hour. Methyl iodide (0.500 mL, 8.00 mmol) was added to the mixture, and the mixture was stirred for 2 hours at room temperature. The solvent was distilled off under reduced pressure, the residue was purified by silica gel column chromatography-(hexane-ethyl acetate) to give compound c78 (36.0 mg, 38% yield).

(814) [M+H]=253.95, Method Condition 3: retention time 1.87 min

(815) Step 9 Preparation of Compound c79

(816) Compound c79 (36.0 mg, 0.142 mmol) was dissolved in dichloromethane (2.0 mL), and 69 wt % m-chloroperoxybenzoic acid (74.6 mg, 0.298 mmol) was added under ice-cooling, and the mixture was stirred at room temperature for 18 hours. 69 wt % m-chloroperbenzoic acid (25.0 mg, 0.703 mmol) was stirred for 3.5 hours. 69 wt % m-chloroperoxybenzoic acid (10.0 mg, 0.281 mmol) and stirred for 1.5 hours. The reaction solution was purified by silica gel column chromatography (hexane-ethyl acetate) to give the compound c79 (35.0 mg, 86% yield).

(817) [M+H]=285.90, Method Condition 3: retention time 1.77 min

(818) Step 10 Preparation of Compound c80

(819) Compound c66 (32.4 mg, 0.150 mmol) was dissolved in THF (10 mL) and tertiary butoxy potassium (38.9 mg, 0.347 mmol) was added to the mixture while cooling in ice, and the mixture was stirred for 3 minutes. Compound c79 (33.0 mg, 0.116 mmol) was dissolved in THF (2.0 mL) was added to the mixture while cooling in ice. The mixture was stirred for 2 hours under ice cooling. Water was added to the mixture, and the mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane-ethyl acetate, then chloroform-methanol) to give the compound c80 (33.3 mg, 68% yield).

(820) .sup.1H-NMR (CDCl.sub.3) : 0.79-0.83 (m, 4H), 1.19 (d, J=6.8 Hz, 3H), 1.50-1.61 (m 2H), 1.64-1.73 (m, 2H), 1.97-2.05 (m, 5H), 2.17-2.25 (m, 2H), 3.44 (tt, J=14.9, 4.8 Hz, 3H), 3.69 (s, 3H), 4.12-4.18 (m, 1H), 4.33-4.38 (m, 1H), 5.10-5.16 (m, 1H), 5.64 (brd, J=7.8 Hz, 1H), 8.17 (s, 1H).

(821) [M+H]=421.20, Method Condition 3: retention time 1.80 min

(822) Step 11 Preparation of Compound c81

(823) Compounds c80 (17.0 mg, 0.040 mmol) was dissolved in acetonitrile (3.4 mL), and N-chlorosuccinimide (13.0 mg, 0.095 mmol) was added to the mixture. Then the mixture was stirred 1.5 hours at 30 C. To the reaction mixture N-chlorosuccinimide (13.0 mg, 0.095 mmol) was added and the mixture was stirred for 1.5 hours. The mixture was allowed to stand at room temperature for 14 hours and stirred for 20 minutes at 40 C. Water was added to the reaction mixture while cooling in ice and the mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (chloroform-methanol) to afford Compound c81 (9.0 mg, 49% yield).

(824) .sup.1H-NMR (CDCl.sub.3) : 0.79-0.81 (m, 4H), 1.20 (d, J=6.8 Hz, 3H), 1.52-1.73 (m, 4H), 1.95-2.03 (m, 5H), 2.16-2.23 (m, 2H), 3.39-3.48 (m, 3H), 3.68 (s, 3H), 4.11-4.19 (m, 1H), 4.38-4.43 (m, 1H), 5.24-5.30 (m, 1H), 5.66 (brd, J=7.0 Hz, 1H).

(825) [M+H]=455.20, Method Condition 3: retention time 2.12 min

(826) Like the above embodiment, Compound I-001-I-748 were prepared. The chemical structure and chemical data are shown below.

(827) TABLE-US-00001 TABLE 1 Retention Method time Example Condition (minute) [M + H] No. Structure or NMR I-001 1H-NMR (CDCl3) : 0.36 (m, 2H), 0.67 (m, 2H), 1.25 (d, J = 6.7 Hz, 3H), 1.42 (s, 9H), 2.86 (dd, J = 15.1, 6.8 Hz, 1H), 3.16 (dd, J = 15.1, 3.3 Hz, 1H), 3.80 (d, J = 7.0 Hz, 2H), 4.10 (m, 1H), 4.88 (brs, 1H), 6.87 (dd, J = 9.0, 3.0 Hz, 1H), 7.01 (d, J = 3.0 Hz, 1H), 7.22 (d, J = 9.0 Hz, 1H), 7.89 (s, 1H). I-002 2 2.15 409.3 I-003 2 2.88 421.5 I-004 2 2.32 363 I-005 4 2.56 362.3 I-006 4 2.48 363.1

(828) TABLE-US-00002 TABLE 2 I-007 0 4 2.69 391 I-008 2 2.14 403.3 I-009 2 2.44 363.4 I-010 2 2.61 376.3 I-011 4 2.6 377.4 I-012 4 2.39 420.3 I-013 4 2.13 411.1 I-014 4 2.54 434.3

(829) TABLE-US-00003 TABLE 3 I-015 4 2.26 425.1 I-016 4 2.68 393.2 I-017 0 4 2.46 398.1 I-018 4 2.22 404.4 I-019 4 2.09 335.4 I-020 4 2.25 389.1 I-021 4 2.38 364.4 I-022 4 2.38 476.5

(830) TABLE-US-00004 TABLE 4 I-023 4 2.37 472.1 I-024 4 2.2 421.4 I-025 4 2.23 436.4 I-026 4 2.15 405.6 I-027 0 4 1.69 437.5 I-028 4 2.62 443.4 I-029 4 2.45 438.4 I-030 4 2.06 357.1

(831) TABLE-US-00005 TABLE 5 I-031 4 1.97 389.2 I-032 4 2.31 423.1 I-033 4 2.55 456.9 I-034 4 2.18 403.5 I-035 4 2.57 432.8 I-036 4 2.19 427.4 I-037 0 4 2.31 405.1 I-038 4 2.62 421.1

(832) TABLE-US-00006 TABLE 6 I-039 4 2.3 423.2 I-040 4 2.79 431.2 I-041 4 2.49 434.4 I-042 4 2.29 409.6 I-043 4 1.99 411.6 I-044 4 2.26 408.5 I-045 4 2.14 407.2 I-046 4 2.47 425

(833) TABLE-US-00007 TABLE 7 I-047 0 4 1.79 441.2 I-048 4 2.29 418.9 I-049 4 2.29 419 I-050 4 2.18 421.5 I-051 2 1.96 416.1 I-052 4 2.52 447.2 I-053 4 2.34 431 I-054 4 2.47 427.2

(834) TABLE-US-00008 TABLE 8 I-055 4 2.29 411 I-056 4 2.32 441.6 I-057 0 4 2.32 441.5 I-058 4 1.97 420.9 I-059 4 2.29 421 I-060 4 1.97 420.9 I-061 4 2.29 421.2 I-062 4 2.1 393.1

(835) TABLE-US-00009 TABLE 9 I-063 2 2.21 407.1 I-064 4 2.27 409.2 I-065 2 2.15 423.2 I-066 4 2.36 425.2 I-067 0 4 1.96 408.3 I-068 4 2.06 414.2 I-069 2 1.89 418 I-070 2 2.15 421.2

(836) TABLE-US-00010 TABLE 10 I-071 4 2.14 439.2 I-072 2 1.97 465 I-073 2 2.36 493.2 I-074 4 2.12 383.6 I-075 4 2.28 399.5 I-076 3 2.07 383.2 I-077 00 3 2.21 399.5

(837) TABLE-US-00011 TABLE 11 I-078 01 3 2.51 425.33 I-079 02 2 2.03 422.15 I-080 03 3 1.79 489 I-081 04 2 2.05 416.2 I-082 05 3 1.64 449 I-083 06 3 2.72 441.28 I-084 07 3 2.55 441.31 I-085 08 3 2.44 441.33

(838) TABLE-US-00012 TABLE 12 I-086 09 3 2.17 397 I-087 0 3 2.31 413 I-088 3 2.18 397.1 I-089 3 2.32 413 I-090 2 1.93 461.05 I-091 2 1.45 451.1 I-092 2 1.83 422.95

(839) TABLE-US-00013 TABLE 13 I-093 4 1.94 411.25 I-094 3 1.91 493 I-095 2 1.81 423.05 I-096 2 1.76 435.4 I-097 0 3 2.23 417 I-098 3 2.36 433.3 I-099 3 1.61 411.3 I-100 3 2.27 413

(840) TABLE-US-00014 TABLE 14 I-101 3 2.02 379.1 I-102 4 2.34 387.3 I-103 3 2.09 404 I-104 4 2.51 403.2 I-105 4 2.23 394.3

(841) TABLE-US-00015 TABLE 15 I-106 4 2.58 446

(842) TABLE-US-00016 TABLE 16 I-107 0 4 2.23 417.0 I-108 4 2.36 433.3 I-109 4 1.61 411.3 I-110 4 2.27 413.0 I-111 4 2.02 379.1

(843) TABLE-US-00017 TABLE 17 I-112 2 2.37 459.1 I-113 2 2.60 441.1 I-114 2 2.50 441.1 I-115 4 2.13 415.0 I-116 4 2.25 430.9

(844) TABLE-US-00018 TABLE 18 I-117 0 2 2.31 425.2 I-118 2 2.21 423.0 I-119 2 2.46 437.1 I-120 2 2.03 471.3 I-121 2 2.39 465.1

(845) TABLE-US-00019 TABLE 19 I-122 2 2.45 425.0 I-123 2 2.18 447.0 I-124 2 2.27 401.0 I-125 2 2.35 437.1 I-126 4 1.88 378.0

(846) TABLE-US-00020 TABLE 20 I-127 0 4 2.18 395.0 I-128 4 2.02 377.0 I-129 2 1.87 477.3 I-130 2 1.97 439.3 I-131 2 2.62 561.2

(847) TABLE-US-00021 TABLE 21 I-132 4 2.58 429.6 I-133 4 2.22 394.9 I-134 2 2.01 441.1 I-135 4 2.01 378.4 I-136 4 2.18 434.9

(848) TABLE-US-00022 TABLE 22 I-137 0 4 2.30 450.9 I-138 4 2.20 411.0 I-139 4 2.09 399.0 I-140 4 2.01 411.0 I-141 4 2.67 445.0

(849) TABLE-US-00023 TABLE 23 I-142 2 2.47 467.1 I-143 2 2.19 447.3 I-144 4 1.98 395.9 I-145 4 2.00 453.6 I-146 4 20.10 452.2

(850) TABLE-US-00024 TABLE 24 I-147 0 4 2.16 400.0 I-148 2 1.54 393.1 I-149 2 2.14 464.1 I-150 2 2.05 462.1 I-151 4 2.17 433.0

(851) TABLE-US-00025 TABLE 25 I-152 4 2.38 451.0 I-153 4 2.43 411.0 I-154 4 2.17 409.0 I-155 4 2.54 423.0 I-156 4 2.46 423.0

(852) TABLE-US-00026 TABLE 26 I-157 0 4 2.02 380.0 I-158 2 2.15 432.1 I-159 2 1.62 411.0 I-160 4 1.64 429.0 I-161 2 2.07 462.1

(853) TABLE-US-00027 TABLE 27 I-162 2 2.07 462.1 I-163 4 1.99 397.9 I-164 4 2.11 416.0 I-165 4 2.16 397.9 I-166 5 2.32 473.1

(854) TABLE-US-00028 TABLE 28 I-167 0 4 2.27 450.2 I-168 4 2.38 459.0 I-169 4 1.99 415.8 I-170 4 2.21 433.9 I-171 2 1.52 394.1

(855) TABLE-US-00029 TABLE 29 I-172 4 1.95 391.9 I-173 4 2.21 393.9 I-174 4 1.89 396.3 I-175 2 2.02 458.1 I-176 2 1.85 452.1

(856) TABLE-US-00030 TABLE 30 I-177 00 2 2.20 393.2 I-178 01 2 2.11 394.2 I-179 02 2 2.00 394.4 I-180 03 4 2.09 433.9 I-181 04 4 2.30 451.9

(857) TABLE-US-00031 TABLE 31 I-182 05 4 2.35 412.0 I-183 06 2 2.27 420.5 I-184 07 2 2.14 448.5 I-185 08 2 1.95 430.4 I-186 09 2 2.22 412.3

(858) TABLE-US-00032 TABLE 32 I-187 0 4 1.62 452.1 I-188 4 2.23 486.1 I-189 4 2.08 472.1 I-190 4 2.05 424.2 I-191 4 2.00 412.0

(859) TABLE-US-00033 TABLE 33 I-192 4 1.87 431.0 I-193 4 2.13 429.9 I-194 4 2.02 412.0 I-195 4 1.80 439.9 I-196 4 2.39 408.0

(860) TABLE-US-00034 TABLE 34 I-197 0 4 2.10 442.0 I-198 4 2.38 420.0 I-199 4 1.61 422.0 I-200 4 2.05 406.0 I-201 4 2.14 424.0

(861) TABLE-US-00035 TABLE 35 I-202 4 1.93 430.0 I-203 4 2.03 448.0 I-204 4 2.18 464.0 I-205 4 1.87 417.6 I-206 4 1.89 432.2

(862) TABLE-US-00036 TABLE 36 I-207 0 4 2.50 469.9 I-208 2 1.89 441.2 I-209 2 2.18 408.2 I-210 2 2.27 412.3 I-211 4 1.75 436.0

(863) TABLE-US-00037 TABLE 37 I-212 4 2.36 414.0 I-213 4 2.23 449.9 I-214 4 2.38 432.0 I-215 4 1.80 427.6 I-216 4 2.00 380.0

(864) TABLE-US-00038 TABLE 38 I-217 0 4 1.98 416.0 I-218 4 2.20 442.0 I-219 4 2.09 456.0 I-220 4 2.06 456.0 I-221 4 2.32 474.0

(865) TABLE-US-00039 TABLE 39 I-222 4 1.71 454.0 1-223 4 1.92 426.0 1-224 4 1.86 406.0 1-225 4 1.97 398.0 I-226 4 1.97 433.9

(866) TABLE-US-00040 TABLE 40 I-227 0 4 1.95 455.0 I-228 4 1.78 441.0 I-229 4 1.52 421.0 I-230 4 1.62 393.0 I-231 4 1.45 379.0

(867) TABLE-US-00041 TABLE 41 I-232 4 2.35 425.3 I-233 4 2.31 412.2 I-234 4 1.86 422.6 I-235 4 1.87 440.2 I-236 4 2.15 486.2

(868) TABLE-US-00042 TABLE 42 I-237 0 4 2.31 498.3 I-238 2 2.20 424.2 I-239 4 2.13 448.1 I-240 4 2.44 426.2 I-241 4 1.99 459.4

(869) TABLE-US-00043 TABLE 43 I-242 4 2.56 420.0 I-243 4 1.95 436.0 I-244 4 2.77 434.0 I-245 4 2.40 406.0 I-246 4 1.83 422.0

(870) TABLE-US-00044 TABLE 44 I-247 0 4 1.83 422.0 I-248 4 2.40 452.0 I-249 4 2.24 438.0 I-250 4 1.87 366.0 I-251 4 1.77 426.9

(871) TABLE-US-00045 TABLE 45 I-252 2 2.34 474.2 I-253 2 2.31 474.2 I-254 4 2.16 477.1 I-255 4 1.60 391.4 I-256 4 1.68 410.1

(872) TABLE-US-00046 TABLE 46 I-257 0 4 1.63 405.2 I-258 4 2.24 406.2 I-259 2 2.07 436.4 I-260 2 2.05 436.4 I-261 2 2.61 434.3

(873) TABLE-US-00047 TABLE 47 I-262 2 2.24 426.2 I-263 2 2.19 447.2 I-264 2 2.11 445.2 I-265 4 2.01 419.6 I-266 4 1.74 409.6

(874) TABLE-US-00048 TABLE 48 I-267 0 4 1.76 427.2 I-268 4 1.93 445.6 I-269 4 1.76 408.3 I-270 4 1.81 422.3 I-271 2 1.85 445.2

(875) TABLE-US-00049 TABLE 49 I-272 2 2.15 400.0 I-273 2 1.98 440.1 I-274 2 2.07 472.2 I-275 2 2.08 463.1 I-276 2 2.06 454.1

(876) TABLE-US-00050 TABLE 50 I-277 00 2 2.07 454.1 I-278 01 2 2.19 455.1 I-279 02 2 2.41 408.2 I-280 03 4 2.08 436.1 I-281 04 4 2.06 436.1

(877) TABLE-US-00051 TABLE 51 I-282 05 4 1.67 404.1 I-283 06 4 1.69 464.2 I-284 07 4 2.06 431.4 I-285 08 2 2.05 425.4 I-286 09 4 1.99 444.3

(878) TABLE-US-00052 TABLE 52 I-287 0 4 1.68 423.1 I-288 4 1.60 430.1 I-289 4 1.68 423.1 I-290 2 2.02 472.6 I-291 2 2.10 457.2

(879) TABLE-US-00053 TABLE 53 I-292 5 2.20 406.1 I-293 4 1.53 421.9 I-294 4 1.52 422.0 I-295 4 2.10 423.9 I-296 4 2.10 423.9

(880) TABLE-US-00054 TABLE 54 I-297 0 4 1.97 434.2 I-298 4 1.86 410.0 I-299 4 2.11 412.0 I-300 4 1.61 424.2 I-301 4 1.87 431.2

(881) TABLE-US-00055 TABLE 55 I-302 4 1.97 433.0 I-303 4 2.01 447.2 I-304 4 1.93 441.2 I-305 4 2.29 446.0 I-306 4 2.00 411.9

(882) TABLE-US-00056 TABLE 56 I-307 0 4 1.69 408.0 I-308 4 2.24 406.0

(883) TABLE-US-00057 TABLE 57 I-309 2 2.10 391.1 I-310 4 2.32 407.3 I-311 2 1.70 393.2 I-312 2 1.96 449.0 I-313 2 2.19 387.0

(884) TABLE-US-00058 TABLE 58 I-314 2 2.00 383.2 I-315 2 1.77 393.2 I-316 2 1.90 419.0 I-317 0 2 2.49 393.1 I-318 2 1.87 392.5

(885) TABLE-US-00059 TABLE 59 I-319 2 1.95 398.1 I-320 4 2.63 457.0 I-321 2 1.64 421.1 I-322 2 2.03 459.2 I-323 2 1.83 404.1

(886) TABLE-US-00060 TABLE 60 I-324 2 2.25 396.3 I-325 2 1.74 382.5 I-326 2 1.89 411.1 I-327 0 2 2.09 447.0 I-328 2 1.24 410.2

(887) TABLE-US-00061 TABLE 61 I-329 2 1.37 408.3 I-330 2 2.00 414.2 I-331 2 0.94 376.4 I-332 2 2.13 408.4 I-333 2 1.80 390.0

(888) TABLE-US-00062 TABLE 62 I-334 4 2.01 347.0 I-335 2 2.36 379.0 I-336 2 2.30 359.0 I-337 0 2 2.08 408.0 I-338 2 2.21 383.2

(889) TABLE-US-00063 TABLE 63 I-339 2 2.00 432.2 I-340 2 2.18 453.2 I-341 2 2.36 434.1 I-342 2 2.23 487.2 I-343 2 1.86 444.3

(890) TABLE-US-00064 TABLE 64 I-344 2 2.20 453.2 I-345 2 2.33 434.4 I-346 2 2.06 445.2 I-347 0 2 2.04 445.2 I-348 2 2.00 451.2

(891) TABLE-US-00065 TABLE 65 I-349 2 2.44 488.2 I-350 2 2.43 488.2 I-351 2 2.12 489.2 I-352 2 1.18 372.2 I-353 2 1.89 456.2

(892) TABLE-US-00066 TABLE 66 I-354 2 1.92 439.2 I-355 2 2.38 384.2 I-356 3 2.09 420.1 I-357 0 3 2.05 408.1 I-358 2 1.47 366.2

(893) TABLE-US-00067 TABLE 67 I-359 2 1.77 373.2 I-360 2 1.87 439.2 I-361 2 1.75 456.3 I-362 2 1.90 387.2 I-363 2 1.76 423.4

(894) TABLE-US-00068 TABLE 68 I-364 2 1.99 418.1 I-365 2 2.41 423.0 I-366 2 2.44 423.0 I-367 0 2 2.05 383.0 I-368 2 2.37 411.2

(895) TABLE-US-00069 TABLE 69 I-369 2 2.15 397.0 I-370 2 2.16 397.0 I-371 2 1.69 408.2 I-372 2 2.37 399.2 I-373 2 1.66 387.5

(896) TABLE-US-00070 TABLE 70 I-374 2 1.55 399.2 I-375 2 2.14 432.1 I-376 2 2.29 420.1 I-377 00 2 1.75 421.1 I-378 01 2 1.09 362.2

(897) TABLE-US-00071 TABLE 71 I-379 02 2 2.15 403.2 I-380 03 3 2.12 439.1 I-381 04 3 1.73 373.1 I-382 05 2 1.26 426.3 I-383 06 3 2.18 404.1 I-384 07 3 2.13 455.0 I-385 08 3 2.09 455.0 I-386 09 2 1.99 455.4 I-387 0 3 1.90 409.1 I-388 3 2.29 438.0

(898) TABLE-US-00072 TABLE 73 I-389 3 2.29 438.0 I-390 3 2.28 438.0 I-391 2 2.02 419.2 I-392 3 1.49 421.0 I-393 3 1.39 421.0

(899) TABLE-US-00073 TABLE 74 I-394 3 2.40 421.1 I-395 3 2.21 419.1 I-396 3 2.14 455.0 I-397 0 2 2.10 447.2 I-398 2 1.78 447.1

(900) TABLE-US-00074 TABLE 75 I-399 2 2.16 463.2 I-400 2 2.34 421.3 I-401 2 1.94 418.4 I-402 2 2.27 433.3 I-403 2 1.69 435.2

(901) TABLE-US-00075 TABLE 76 I-404 2 2.16 451.3 I-405 2 1.83 439.1 I-406 2 1.61 422.4 I-407 0 2 2.34 464.2 I-408 2 2.35 464.2

(902) TABLE-US-00076 TABLE 77 I-409 2 1.79 427.3 I-410 2 1.92 441.3 I-411 2 2.09 463.0 I-412 2 1.74 427.3 I-413 2 2.27 432.4

(903) TABLE-US-00077 TABLE 78 I-414 2 1.97 396.2 I-415 3 2.28 400.1 I-416 2 2.07 396.0 I-417 0 2 1.84 388.0 I-418 3 2.28 438.0

(904) TABLE-US-00078 TABLE 79 I-419 3 1.90 374.0 I-420 3 1.81 400.0 I-421 4 2.18 364.0 I-422 4 2.03 419.3 I-423 2 1.94 410.0

(905) TABLE-US-00079 TABLE 80 I-424 2 1.96 335.1 I-425 2 2.07 499.2 I-426 2 1.92 387.2 I-427 0 2 1.78 398.2 I-428 2 1.82 387.2

(906) TABLE-US-00080 TABLE 81 I-429 2 1.98 420.2 I-430 2 1.92 409.2 I-431 2 1.68 411.1 I-432 2 1.38 410.2 I-433 2 2.20 438.3

(907) TABLE-US-00081 TABLE 82 I-434 2 1.08 410.3 I-435 2 1.95 419.2 I-436 2 1.95 419.2 I-437 0 2 2.15 489.4 I-438 2 1.83 444.2

(908) TABLE-US-00082 TABLE 83 I-439 2 2.20 461.0 I-440 2 1.87 427.2 I-441 2 2.02 445.1 I-442 2 2.23 386.2 I-443 2 2.10 496.3

(909) TABLE-US-00083 TABLE 84 I-444 2 1.86 387.0 I-445 2 2.36 422.2 I-446 2 2.04 453.2 I-447 0 2 1.88 387.2 I-448 2 1.93 395.2

(910) TABLE-US-00084 TABLE 85 I-449 2 2.25 415.3 I-450 2 1.88 391.2 I-451 2 2.10 401.2 I-452 2 1.61 433.2 I-453 2 1.54 347.4

(911) TABLE-US-00085 TABLE 86 I-454 2 1.88 387.4 I-455 2 2.32 475.2 I-456 2 1.98 396.2 I-457 0 2 2.04 453.2 I-458 2 1.10 374.3

(912) TABLE-US-00086 TABLE 87 I-459 2 1.81 423.2 I-460 2 1.92 439.3 I-461 2 2.14 422.2 I-462 2 1.90 431.3 I-463 2 2.04 428.2

(913) TABLE-US-00087 TABLE 88 I-464 2 1.73 427.1 I-465 2 1.64 409.2 I-466 2 2.30 446.4 I-467 0 2 1.97 439.2 I-468 4 1.83 439.0

(914) TABLE-US-00088 TABLE 89 I-469 2 1.98 409.2 I-470 2 1.79 444.3 I-471 2 1.72 361.2 I-472 2 1.99 427.2 I-473 2 1.97 427.2

(915) TABLE-US-00089 TABLE 90 I-474 2 1.97 427.2

(916) TABLE-US-00090 TABLE 91 I-475 4 1.60 389.2 I-476 4 1.83 403.2 I-477 00 4 1.90 439.4 I-478 01 4 1.92 439.4 I-479 02 4 1.72 391.1

(917) TABLE-US-00091 TABLE 92 I-480 03 4 2.07 439.2 I-481 04 4 1.98 425.2 I-482 05 4 2.18 419.4 I-483 06 4 1.79 391.0 I-484 07 4 1.73 413.1

(918) TABLE-US-00092 TABLE 93 I-485 08 4 1.71 409.2 I-486 09 4 1.89 417.7 I-487 0 4 1.63 394.5 I-488 4 1.90 411.2 I-489 4 1.50 402.3

(919) TABLE-US-00093 TABLE 94 I-490 4 1.79 410.3 I-491 4 1.62 391.5 I-492 2 1.69 479.1 I-493 2 1.81 405.6 I-494 2 1.79 405.5

(920) TABLE-US-00094 TABLE 95 I-495 2 1.64 403.3 I-496 2 1.85 417.3 I-497 0 2 1.89 453.3 I-498 2 1.95 445.2 I-499 2 1.76 427.2

(921) TABLE-US-00095 TABLE 96 I-500 2 1.87 441.2 I-501 2 2.05 453.3 I-502 2 1.88 417.2 I-503 2 1.99 453.1 I-504 2 2.02 459.1

(922) TABLE-US-00096 TABLE 97 I-505 2 1.96 405.2 I-506 2 1.33 390.3 I-507 0 2 1.88 408.1 I-508 2 2.27 471.2 I-509 2 1.99 431.3

(923) TABLE-US-00097 TABLE 98 I-510 2 2.01 425.1 I-511 2 2.01 481.3 I-512 2 1.12 401.3 I-513 2 1.09 389.6 I-514 2 1.22 415.6

(924) TABLE-US-00098 TABLE 99 I-515 2 1.50 443.6 I-516 2 1.91 409.1 I-517 0 2 2.02 423.4 I-518 2 2.04 471.5 I-519 4 1.54 377.0

(925) TABLE-US-00099 TABLE 100 I-520 4 1.58 377.2

(926) TABLE-US-00100 TABLE 101 I-521 2 2.04 407.2 I-522 3 2.32 423.2 I-523 3 1.97 389.2 I-524 3 2.03 414.2 I-525 3 2.04 414.2

(927) TABLE-US-00101 TABLE 102 I-526 3 2.27 423.2 I-527 0 3 1.93 419.2 I-528 3 2.07 419.2 I-529 3 2.40 431.2 I-530 3 1.85 421.2

(928) TABLE-US-00102 TABLE 103 I-531 2 1.99 414.25 I-532 3 2.20 403.2 I-533 3 2.26 417.2 I-534 3 2.12 403.2 I-535 3 2.23 430.1

(929) TABLE-US-00103 TABLE 104 I-536 3 2.29 429.2 I-537 0 3 2.23 495.2 I-538 2 1.89 408.6 I-539 2 2.32 542.2 I-540 2 2.20 443.2

(930) TABLE-US-00104 TABLE 105 I-541 2 2.34 423.2 I-542 2 2.40 405.3 I-543 2 2.71 455.3 I-544 2 2.67 421.3 I-545 4 2.37 457.2

(931) TABLE-US-00105 TABLE 106 I-546 4 2.25 464.2

(932) TABLE-US-00106 TABLE 107 I-547 0 2 2.43 427.2 I-548 3 2.08 414.3 I-549 3 2.39 427.2 I-550 3 2.36 419.3 I-551 2 2.07 430.5

(933) TABLE-US-00107 TABLE 108 I-552 2 2.22 448.3 I-553 3 2.18 430.1 I-554 3 1.84 424.0 I-555 3 2.26 448.1

(934) TABLE-US-00108 TABLE 109 No. [M + H] I-556 3 2.00 424 .2 I-557 0 3 1.99 424.2 I-558 3 1.94 452.3 I-559 3 1.62 390.2 I-560 3 1.75 404.3

(935) TABLE-US-00109 TABLE 110 I-561 3 1.67 416.1 I-562 3 1.88 418.3 I-563 3 1.28 391.2 I-564 2 1.45 390.2 I-565 4 1.80 438.3

(936) TABLE-US-00110 TABLE 111 I-566 2 1.57 404.2 I-567 0 2 1.59 416.5 I-568 3 1.71 416.3 I-569 2 1.52 424.2 I-570 2 1.28 376.1

(937) TABLE-US-00111 TABLE 112 I-571 3 1.88 444.2 I-572 3 2.12 430.1 I-573 2 1.72 388.3 I-574 2 1.56 386.3 I-575 2 1.45 437.3

(938) TABLE-US-00112 TABLE 113 I-576 2 1.10 415.3 I-577 00 2 1.84 406.2 I-578 01 2 2.17 434.3 I-579 02 2 1.57 404.3 I-580 03 2 1.44 438.2

(939) TABLE-US-00113 TABLE 114 I-581 04 3 1.87 466.2 I-582 05 3 2.06 422.2 I-583 06 2 1.52 374.3 I-584 07 2 1.64 372.2 I-585 08 2 1.67 388.3

(940) TABLE-US-00114 TABLE 115 I-586 09 3 2.08 438.2 I-587 0 2 1.98 414.2 I-588 2 1.98 414.5 I-589 2 1.08 423.2 I-590 3 1.69 439.2

(941) TABLE-US-00115 TABLE 116 I-591 2 1.15 387.3 I-592 2 1.65 439.3 I-593 3 1.48 439.2 I-594 3 1.27 439.2 I-595 3 1.45 440.2

(942) TABLE-US-00116 TABLE 117 I-596 3 2.09 456.1 I-597 0 2 1.13 376.2 I-598 3 2.23 487.3 I-599 3 1.84 395.2 I-600 3 2.26 470.2

(943) TABLE-US-00117 TABLE 118 I-601 3 1.99 408.2 I-602 3 2.11 422.1 I-603 2 2.33 459.2 I-604 2 2.03 424.2 I-605 3 2.19 469.1

(944) TABLE-US-00118 TABLE 119 I-606 3 1.76 404.2 I-607 0 3 1.33 405.2 I-608 3 2.07 457.1 I-609 2 2.14 494.2 I-610 3 2.19 442.1

(945) TABLE-US-00119 TABLE 120 I-611 2 2.12 438.3 I-612 2 1.85 456.2 I-613 2 1.62 492.2 I-614 2 2.21 498.3 I-615 4 1.84 464.3

(946) TABLE-US-00120 TABLE 121 I-616 2 1.56 495.3 I-617 0 3 2.18 445.1 I-618 3 2.20 496.0 I-619 2 2.15 418.2 I-620 2 2.31 487.2

(947) TABLE-US-00121 TABLE 122 I-621 2 2.07 404.5 I-622 3 2.13 443.1 I-623 2 2.01 494.2 I-624 3 1.99 445.1 I-625 2 2.16 435.1

(948) TABLE-US-00122 TABLE 123 I-626 2 2.22 452.2 I-627 0 4 1.97 462.3 I-628 2 1.90 478.2 I-629 2 1.99 528.2 I-630 2 2.03 400.2

(949) TABLE-US-00123 TABLE 124 I-631 2 2.09 491.5 I-632 3 2.07 435.1 I-633 2 2.03 498.2 I-634 3 2.23 471.2 I-635 2 2.05 426.3

(950) TABLE-US-00124 TABLE 125 I-636 2 2.23 435.3 I-637 0 3 2.15 478.1 I-638 3 2.14 398.0 I-639 2 2.30 452.3 I-640 2 1.92 521.2

(951) TABLE-US-00125 TABLE 126 I-641 3 1.92 409.1 I-642 4 1.96 462.3 I-643 2 2.05 498.3 I-644 2.13 475.3 I-645 2 1.91 499.5

(952) TABLE-US-00126 TABLE 127 I-646 3 2.10 425.2 I-647 0 3 2.23 439.2 I-648 2 2.14 420.2 I-649 2 2.33 472.3 I-650 3 1.91 466.1

(953) TABLE-US-00127 TABLE 128 I-651 2 2.15 442.2 I-652 2 2.34 488.3 I-653 3 2.05 469.1 I-654 2 2.00 513.4 I-655 2 2.28 454.2

(954) TABLE-US-00128 TABLE 129 I-656 2 1.90 514.2 I-657 0 4 1.97 461.3 I-658 3 2.05 462.1 I-659 2 2.13 477.1 I-660 2 1.17 461.7

(955) TABLE-US-00129 TABLE 130 I-661 3 2.13 466.2 I-662 3 2.23 451.2 I-663 2 2.03 411.3 I-664 3 2.18 451.2 I-665 2 2.06 426.3

(956) TABLE-US-00130 TABLE 131 I-666 3 2.02 482.2 I-667 0 3 1.91 421.1 I-668 2 2.02 454.4 I-669 2 1.77 499.2 I-670 2 1.88 463.2

(957) TABLE-US-00131 TABLE 132 I-671 2 2.28 474.2 I-672 2 2.23 478.5 I-673 3 1.96 463.1 I-674 4 1.98 479.3 I-675 2 2.17 475.1

(958) TABLE-US-00132 TABLE 133 I-676 3 2.20 480.1 I-677 00 3 1.97 444.2 I-678 01 2 2.21 460.1 I-679 02 2 1.87 451.4 I-680 03 2 1.98 506.2

(959) TABLE-US-00133 TABLE 134 I-681 04 3 2.29 502.1 I-682 05 4 2.12 436.3 I-683 06 2 2.35 474.2 I-684 07 4 1.98 461.3 I-685 08 2 1.97 426.7

(960) TABLE-US-00134 TABLE 135 I-686 09 3 2.27 443.0 I-687 0 2 1.99 479.4 I-688 4 2.09 478.3 I-689 2 2.01 435.1 I-690 3 1.99 477.1

(961) TABLE-US-00135 TABLE 136 I-691 2 2.10 444.1 I-692 2 2.00 424.4 I-693 3 2.24 487.1 I-694 2 1.81 409.1 I-695 2 1.38 421.2

(962) TABLE-US-00136 TABLE 137 I-696 4 2.59 494.1 I-697 0 2 1.99 439.2 I-698 2 2.04 426.7 I-699 2 1.70 492.5 I-700 2 2.01 502.2

(963) TABLE-US-00137 TABLE 138 I-701 2 1.90 477.0 I-702 4 2.11 476.3 I-703 3 2.11 487.1 I-704 3 1.85 454.1 I-705 3 2.08 437.1 I-706 2 1.94 460.2 I-707 0 3 1.92 444.2 I-708 3 2.18 487.1 1-709 2 1.57 440.3 I-710 2 2.29 471.4

(964) TABLE-US-00138 TABLE 140 I-711 2 2.12 455.2 I-712 3 1.70 410.1 I-713 2 2.19 488.2 I-714 2 2.06 487.2 I-715 2 2.25 553.4

(965) TABLE-US-00139 TABLE 141 I-716 2 2.08 498.2 I-717 0 2 2.13 476.2 I-718 2 1.87 457.3 I-719 3 1.94 407.1 I-720 3 1.93 415.2

(966) TABLE-US-00140 TABLE 142 I-721 3 1.96 417.1 I-722 4 1.98 461.3 I-723 3 1.97 408.2 I-724 3 2.07 457.1 I-725 2 2.09 458.1

(967) TABLE-US-00141 TABLE 143 I-726 2 2.20 451.3 I-727 0 2 2.38 455.3 I-728 2 2.03 479.2 I-729 2 2.20 463.2 I-730 2 1.96 486.4

(968) TABLE-US-00142 TABLE 144 I-731 2 1.74 477.2 I-732 2 2.11 497.4 I-733 2 2.18 496.2 I-734 3 2.05 420.1 I-735 3 1.91 430.2

(969) TABLE-US-00143 TABLE 145 I-736 3 2.07 447.1 I-737 0 3 2.10 434.2 I-738 3 2.37 530.1 I-739 2 2.29 458.1 I-740 3 2.32 442.1

(970) TABLE-US-00144 TABLE 146 I-741 5 3.85 462.5 I-742 3 2.13 478.1 I-743 2 1.72 412.2 I-744 2 1.35 461.2 I-745 2 1.73 478.3

(971) TABLE-US-00145 TABLE 147 I-746 2 1.91 435.3 I-747 0 2 1.98 487.5 I-748 2 1.96 480.4

(972) In the following general formula (I), the compounds having the following groups can be synthesized in similar methods described in the above working examples.

(973) ##STR00872##

(974) TABLE-US-00146 TABLE 148 X X.sup.1 S X.sup.2 O X.sup.3 N(Me) X.sup.4 N(Et) X.sup.5 N(n-Pr) X.sup.6 N(i-Pr)

(975) TABLE-US-00147 TABLE 149 R.sup.a R.sup.a1 R.sup.a2 R.sup.a3

(976) TABLE-US-00148 TABLE 150 R.sup.b R.sup.b1 F R.sup.b2 Cl R.sup.b3 CN

(977) TABLE-US-00149 TABLE 151 A A.sup.1 A.sup.2 A.sup.3 A.sup.4 A.sup.5 0

(978) TABLE-US-00150 TABLE 152 R.sup.c, R.sup.c R.sup.c1 R.sup.c2 R.sup.c3 R.sup.c4

(979) TABLE-US-00151 TABLE 153 R.sup.d R.sup.d1 R.sup.d2 R.sup.d3

(980) The combination of X, R.sup.a, R.sup.b, A, R.sup.c, and R.sup.d, is any one of the following combinations in the above formula (I):

(981) (X, R.sup.a, R.sup.b, A, R.sup.c, R.sup.d)=(X.sup.1, R.sup.a1, R.sup.b1, A.sup.1, R.sup.c1, R.sup.d1), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.1, R.sup.c1, R.sup.d2), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.1, R.sup.c1, R.sup.d3), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.1, R.sup.c2, R.sup.d1), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.1, R.sup.c2, R.sup.d2), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.1, R.sup.c2, R.sup.d3), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.1, R.sup.c3, R.sup.d1), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.1, R.sup.c3, R.sup.d2), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.1, R.sup.c3, R.sup.d3), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.1, R.sup.c4, R.sup.d1), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.1, R.sup.c4, R.sup.d2), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.1, R.sup.c4, R.sup.d3), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.2, R.sup.c1, R.sup.d1), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.2, R.sup.c1, R.sup.d2), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.2, R.sup.c1, R.sup.d3), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.2, R.sup.c2, R.sup.d1), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.2, R.sup.c2, R.sup.d2), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.2, R.sup.c2, R.sup.d3), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.2, R.sup.c3, R.sup.d1), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.2, R.sup.c3, R.sup.d2), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.2, R.sup.c3, R.sup.d3), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.2, R.sup.c4, R.sup.d1), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.2, R.sup.c4, R.sup.d2), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.2, R.sup.c4, R.sup.d3), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.3, R.sup.c1, R.sup.d1), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.3, R.sup.c1, R.sup.d2), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.3, R.sup.c1, R.sup.d3), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.3, R.sup.c2, R.sup.d1), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.3, R.sup.c2, R.sup.d2), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.3, R.sup.c2, R.sup.d3), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.3, R.sup.c3, R.sup.d1), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.3, R.sup.c3, R.sup.d2), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.3, R.sup.c3, R.sup.d3), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.3, R.sup.c4, R.sup.d1), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.3, R.sup.c4, R.sup.d2), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.3, R.sup.c4, R.sup.d3), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.4, R.sup.c1, R.sup.d1), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.4, R.sup.c1, R.sup.d2), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.4, R.sup.c1, R.sup.d3), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.4, R.sup.c2, R.sup.d1), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.4, R.sup.c2, R.sup.d2), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.4, R.sup.c2, R.sup.d3), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.4, R.sup.c3, R.sup.d1), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.4, R.sup.c3, R.sup.d2), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.4, R.sup.c3, R.sup.d3), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.4, R.sup.c4, R.sup.d1), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.4, R.sup.c4, R.sup.d2), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.4, R.sup.c4, R.sup.d3), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.5, R.sup.c1, R.sup.d1), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.5, R.sup.c1, R.sup.d2), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.5, R.sup.c1, R.sup.d3), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.5, R.sup.c2, R.sup.d1), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.5, R.sup.c2, R.sup.d2), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.5, R.sup.c2, R.sup.d3), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.5, R.sup.c3, R.sup.d1), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.5, R.sup.c3, R.sup.d2), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.5, R.sup.c3, R.sup.d3), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.5, R.sup.c4, R.sup.d1), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.5, R.sup.c4, R.sup.d2), (X.sup.1, R.sup.a1, R.sup.b1, A.sup.5, R.sup.c4, R.sup.d3), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.1, R.sup.c1, R.sup.d1), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.1, R.sup.c1, R.sup.d2), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.1, R.sup.c1, R.sup.d3), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.1, R.sup.c2, R.sup.d1), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.1, R.sup.c2, R.sup.d2), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.1, R.sup.c2, R.sup.d3), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.1, R.sup.c3, R.sup.d1), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.1, R.sup.c3, R.sup.d2), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.1, R.sup.c3, R.sup.d3), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.1, R.sup.c4, R.sup.d1), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.1, R.sup.c4, R.sup.d2), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.1, R.sup.c4, R.sup.d3), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.2, R.sup.c1, R.sup.d1), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.2, R.sup.c1, R.sup.d2), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.2, R.sup.c1, R.sup.d3), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.2, R.sup.c2, R.sup.d1), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.2, R.sup.c2, R.sup.d2), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.2, R.sup.c2, R.sup.d3), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.2, R.sup.c3, R.sup.d1), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.2, R.sup.c3, R.sup.d2), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.2, R.sup.c3, R.sup.d3), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.2, R.sup.c4, R.sup.d1), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.2, R.sup.c4, R.sup.d2), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.2, R.sup.c4, R.sup.d3), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.3, R.sup.c1, R.sup.d1), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.3, R.sup.c1, R.sup.d2), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.3, R.sup.c1, R.sup.d3), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.3, R.sup.c2, R.sup.d1), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.3, R.sup.c2, R.sup.d2), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.3, R.sup.c2, R.sup.d3), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.3, R.sup.c3, R.sup.d1), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.3, R.sup.c3, R.sup.d2), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.3, R.sup.c3, R.sup.d3), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.3, R.sup.c4, R.sup.d1), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.3, R.sup.c4, R.sup.d2), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.3, R.sup.c4, R.sup.d3), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.4, R.sup.c1, R.sup.d1), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.4, R.sup.c1, R.sup.d2), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.4, R.sup.c1, R.sup.d3), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.4, R.sup.c2, R.sup.d1), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.4, R.sup.c2, R.sup.d2), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.4, R.sup.c2, R.sup.d3), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.4, R.sup.c3, R.sup.d1), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.4, R.sup.c3, R.sup.d2), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.4, R.sup.c3, R.sup.d3), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.4, R.sup.c4, R.sup.d1), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.4, R.sup.c4, R.sup.d2), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.4, R.sup.c4, R.sup.d3), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.5, R.sup.c1, R.sup.d1), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.5, R.sup.c1, R.sup.d2), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.5, R.sup.c1, R.sup.d3), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.5, R.sup.c2, R.sup.d1), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.5, R.sup.c2, R.sup.d2), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.5, R.sup.c2, R.sup.d3), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.5, R.sup.c3, R.sup.d1), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.5, R.sup.c3, R.sup.d2), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.5, R.sup.c3, R.sup.d3), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.5, R.sup.c4, R.sup.d1), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.5, R.sup.c4, R.sup.d2), (X.sup.1, R.sup.a1, R.sup.b2, A.sup.5, R.sup.c4, R.sup.d3), (X.sup.1, R.sup.a1, R.sup.b3, A.sup.1, R.sup.c1, R.sup.d1), (X.sup.1, R.sup.a1, R.sup.b3, A.sup.1, R.sup.c1, R.sup.d2), (X.sup.1, R.sup.a1, R.sup.b3, A.sup.1, R.sup.c1, R.sup.d3), (X.sup.1, R.sup.a1, R.sup.b3, A.sup.1, R.sup.c2, R.sup.d1), (X.sup.1, R.sup.a1, R.sup.b3, A.sup.1, R.sup.c2, R.sup.d2), (X.sup.1, R.sup.a1, R.sup.b3, A.sup.1, R.sup.c2, R.sup.d3), (X.sup.1, R.sup.a1, R.sup.b3, A.sup.1, R.sup.c3, R.sup.d1), (X.sup.1, R.sup.a1, R.sup.b3, A.sup.1, R.sup.c3, R.sup.d2), (X.sup.1, R.sup.a1, R.sup.b3, A.sup.1, R.sup.c3, R.sup.d3), (X.sup.1, R.sup.a1, R.sup.b3, A.sup.1, R.sup.c4, R.sup.d1), (X.sup.1, R.sup.a1, R.sup.b3, A.sup.1, R.sup.c4, R.sup.d2), (X.sup.1, R.sup.a1, R.sup.b3, A.sup.1, R.sup.c4, R.sup.d3), (X.sup.1, R.sup.a1, R.sup.b3, A.sup.2, R.sup.c1, R.sup.d1), (X.sup.1, R.sup.a1, R.sup.b3, A.sup.2, R.sup.c1, R.sup.d2), (X.sup.1, R.sup.a1, R.sup.b3, A.sup.2, R.sup.c1, R.sup.d3), (X.sup.1, R.sup.a1, R.sup.b3, A.sup.2, R.sup.c2, R.sup.d1), (X.sup.1, R.sup.a1, R.sup.b3, A.sup.2, R.sup.c2, R.sup.d2), (X.sup.1, R.sup.a1, R.sup.b3, A.sup.2, R.sup.c2, R.sup.d3), (X.sup.1, R.sup.a1, R.sup.b3, A.sup.2, R.sup.c3, R.sup.d1), (X.sup.1, R.sup.a1, R.sup.b3, A.sup.2, R.sup.c3, R.sup.d2), (X.sup.1, R.sup.a1, R.sup.b3, A.sup.2, R.sup.c3, R.sup.d3), (X.sup.1, R.sup.a1, R.sup.b3, A.sup.2, R.sup.c4, R.sup.d1), (X.sup.1, R.sup.a1, R.sup.b3, A.sup.2, R.sup.c4, R.sup.d2), (X.sup.1, R.sup.a1, R.sup.b3, A.sup.2, R.sup.c4, R.sup.d3), (X.sup.1, R.sup.a1, R.sup.b3, A.sup.3, R.sup.c1, R.sup.d1), (X.sup.1, R.sup.a1, R.sup.b3, A.sup.3, R.sup.c1, R.sup.d2), (X.sup.1, R.sup.a1, R.sup.b3, A.sup.3, R.sup.c1, R.sup.d3), (X.sup.1, R.sup.a1, R.sup.b3, A.sup.3, R.sup.c2, R.sup.d1), (X.sup.1, R.sup.a1, R.sup.b3, A.sup.3, R.sup.c2, R.sup.d2), (X.sup.1, R.sup.a1, R.sup.b3, A.sup.3, R.sup.c2, R.sup.d3), (X.sup.1, R.sup.a1, R.sup.b3, A.sup.3, R.sup.c3, R.sup.d1), (X.sup.1, R.sup.a1, R.sup.b3, A.sup.3, R.sup.c3, R.sup.d2), (X.sup.1, R.sup.a1, R.sup.b3, A.sup.3, R.sup.c3, R.sup.d3), (X.sup.1, R.sup.a1, R.sup.b3, A.sup.3, R.sup.c4, R.sup.d1), (X.sup.1, R.sup.a1, R.sup.b3, A.sup.3, R.sup.c4, R.sup.d2), (X.sup.1, R.sup.a1, R.sup.b3, A.sup.3, R.sup.c4, R.sup.d3), (X.sup.1, R.sup.a1, R.sup.b3, A.sup.4, R.sup.c1, R.sup.d1), (X.sup.1, R.sup.a1, R.sup.b3, A.sup.4, R.sup.c1, R.sup.d2), (X.sup.1, R.sup.a1, R.sup.b3, A.sup.4, R.sup.c1, R.sup.d3), (X.sup.1, R.sup.a1, R.sup.b3, A.sup.4, R.sup.c2, R.sup.d1), (X.sup.1, R.sup.a1, R.sup.b3, A.sup.4, R.sup.c2, R.sup.d2), (X.sup.1, R.sup.a1, R.sup.b3, A.sup.4, R.sup.c2, R.sup.d3), (X.sup.1, R.sup.a1, R.sup.b3, A.sup.4, R.sup.c3, R.sup.d1), (X.sup.1, R.sup.a1, R.sup.b3, A.sup.4, R.sup.c3, R.sup.d2), (X.sup.1, R.sup.a1, R.sup.b3, A.sup.4, R.sup.c3, R.sup.d3), (X.sup.1, R.sup.a1, R.sup.b3, A.sup.4, R.sup.c4, 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R.sup.d1), (X.sup.6, R.sup.a3, R.sup.b2, A.sup.5, R.sup.c1, R.sup.d2), (X.sup.6, R.sup.a3, R.sup.b2, A.sup.5, R.sup.c1, R.sup.d3), (X.sup.6, R.sup.a3, R.sup.b2, A.sup.5, R.sup.c2, R.sup.d1), (X.sup.6, R.sup.a3, R.sup.b2, A.sup.5, R.sup.c2, R.sup.d2), (X.sup.6, R.sup.a3, R.sup.b2, A.sup.5, R.sup.c2, R.sup.d3), (X.sup.6, R.sup.a3, R.sup.b2, A.sup.5, R.sup.c3, R.sup.d1), (X.sup.6, R.sup.a3, R.sup.b2, A.sup.5, R.sup.c3, R.sup.d2), (X.sup.6, R.sup.a3, R.sup.b2, A.sup.5, R.sup.c3, R.sup.d3), (X.sup.6, R.sup.a3, R.sup.b2, A.sup.5, R.sup.c4, R.sup.d1), (X.sup.6, R.sup.a3, R.sup.b2, A.sup.5, R.sup.c4, R.sup.d2), (X.sup.6, R.sup.a3, R.sup.b2, A.sup.5, R.sup.c4, R.sup.d3), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.1, R.sup.c1, R.sup.d1), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.1, R.sup.c1, R.sup.d2), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.1, R.sup.c1, R.sup.d3), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.1, R.sup.c2, R.sup.d1), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.1, R.sup.c2, R.sup.d2), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.1, R.sup.c2, R.sup.d3), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.1, R.sup.c3, R.sup.d1), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.1, R.sup.c3, R.sup.d2), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.1, R.sup.c3, R.sup.d3), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.1, R.sup.c4, R.sup.d1), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.1, R.sup.c4, R.sup.d2), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.1, R.sup.c4, R.sup.d3), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.2, R.sup.c1, R.sup.d1), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.2, R.sup.c1, R.sup.d2), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.2, R.sup.c1, R.sup.d3), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.2, R.sup.c2, R.sup.d1), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.2, R.sup.c2, R.sup.d2), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.2, R.sup.c2, R.sup.d3), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.2, R.sup.c3, R.sup.d1), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.2, R.sup.c3, R.sup.d2), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.2, R.sup.c3, R.sup.d3), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.2, R.sup.c4, R.sup.d1), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.2, R.sup.c4, R.sup.d2), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.2, R.sup.c4, R.sup.d3), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.3, R.sup.c1, R.sup.d1), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.3, R.sup.c1, R.sup.d2), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.3, R.sup.c1, R.sup.d3), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.3, R.sup.c2, R.sup.d1), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.3, R.sup.c2, R.sup.d2), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.3, R.sup.c2, R.sup.d3), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.3, R.sup.c3, R.sup.d1), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.3, R.sup.c3, R.sup.d2), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.3, R.sup.c3, R.sup.d3), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.3, R.sup.c4, R.sup.d1), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.3, R.sup.c4, R.sup.d2), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.3, R.sup.c4, R.sup.d3), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.4, R.sup.c1, R.sup.d1), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.4, R.sup.c1, R.sup.d2), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.4, R.sup.c1, R.sup.d3), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.4, R.sup.c2, R.sup.d1), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.4, R.sup.c2, R.sup.d2), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.4, R.sup.c2, R.sup.d3), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.4, R.sup.c3, R.sup.d1), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.4, R.sup.c3, R.sup.d2), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.4, R.sup.c3, R.sup.d3), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.4, R.sup.c4, R.sup.d1), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.4, R.sup.c4, R.sup.d2), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.4, R.sup.c4, R.sup.d3), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.5, R.sup.c1, R.sup.d1), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.5, R.sup.c1, R.sup.d2), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.5, R.sup.c1, R.sup.d3), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.5, R.sup.c2, R.sup.d1), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.5, R.sup.c2, R.sup.d2), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.5, R.sup.c2, R.sup.d3), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.5, R.sup.c3, R.sup.d1), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.5, R.sup.c3, R.sup.d2), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.5, R.sup.c3, R.sup.d3), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.5, R.sup.c4, R.sup.d1), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.5, R.sup.c4, R.sup.d2), (X.sup.6, R.sup.a3, R.sup.b3, A.sup.5, R.sup.c4, R.sup.d3).

(982) The Biological Test Examples of the present invention are described as follows.

(983) Preparation 1: Preparation of Recombinant Human ACC2

(984) After a cDNA encoding human ACC2 (27 amino acid residue to 2458 amino acid residues from the N-terminus) was cloned from human kidney cDNA library (Clontech), human ACC2 gene containing His-tag sequence at 5 terminus was inserted into pFastBac1 (Invitrogen). Recombinant baculovirus was generated using Bac-to-Bac baculovirus expression system (Invitrogen) according to the manufacturer's protocol. To express human ACC2, Sf-9 cells were infected with recombinant baculovirus. After infected cells were disrupted, the filtrated lysate was subjected to Ni-affinity chromatography and anion-exchange chromatography. The fractions containing human ACC2 protein were pooled as recombinant human ACC2 solution.

(985) Preparation 2: Preparation of Recombinant Human ACC1

(986) After a cDNA encoding human ACC1 (1 amino acid residue to 2346 amino acid residues from the N-terminus) was cloned from human liver cDNA library (BioChain), human ACC1 gene containing myc-tag and His-tag sequence at 3 terminus was inserted into pIEXBAC3 (Novagen). Recombinant baculovirus was generated using FlashBACGOLD system (Oxford Expression Technologies) according to the manufacturer's protocol. To express human ACC1, Sf-9 cells were infected with recombinant baculovirus. After infected cells were disrupted, the filtrated lysate was subjected to Ni-affinity chromatography and anion-exchange chromatography. The fractions containing human ACC1 protein were pooled as recombinant human ACC1 solution.

Test Example 1

The Measurement of Inhibitory Activity on Human ACC1 and the ACC2

(987) Recombinant human ACC1 and recombinant human ACC2, which were prepared by the method mentioned above, were preincubated with assay buffer solution (50 mM HEPES-KOH (pH 7.4), 10 mM magnesium chloride, 6-10 mM potassium citrate, 4 mM reduced form of glutathione, 1.5 mg/ml bovine serum albumin) for one hour. Then, 0.2 L of each this invention compound solution (in DMSO) were dispensed to 384-well microplate, 5 L of the preincubated enzyme solution and 5 L of substrate solution (50 mM HEPES-KOH (pH 7.4), 1 mM ATP, 0.8 mM acetyl CoA and 25-50 mM potassium bicarbonate) were added to microplate. After centrifugation and shaking, the reaction mixtures were incubated in a humidified box at room temperature for 1 to 3 hours. After the incubation, the enzyme reactions were stopped by the addition of EDTA. Then, after the samples were cocrystallized with CHCA (-cyano-4-hydroxy cinnamic acid) matrices on MALDI target plate, by using the matrix assist laser deionization time-of-flight mass spectrometer (MALDI-TOF MS), samples were measured in reflector negative mode. Deprotonated ions of acetyl CoA (AcCoA) of substrate and malonyl CoA (MalCoA) of the reaction product were detected, then, the conversion rates of acetyl CoA to malonyl CoA was calculated by the intensity of [MalCoA-H]/(Intensity of [MalCoA-H]+Intensity of [AcCoA-H]) using each signal strength. The 50% inhibitory concentration (IC50) was calculated from the inhibition rate of the enzymatic reaction at each concentration of the compounds. In addition, potassium citrate concentrations in assay buffer solution, potassium hydrogen carbonate concentrations in substrate solution and incubation time were adjusted by each lot of enzyme.

(988) The 50% inhibitory concentration (IC50) on human ACC1 of Compound I-001, I-002, I-003, I-037, I-058, I-067, I-079, I-081, I-091, I-098, I-103 and I-106 were measured, that of these compounds was more than 100 M.

(989) The inhibitory activity on human ACC2 of the each present compound is described in the following tables 154-159.

(990) TABLE-US-00152 TABLE 154 Example IC50 No. (uM) I-001 0.071 I-002 0.770 I-004 3.730 I-005 0.184 I-006 0.348 I-007 1.390 I-008 0.220 I-009 1.060 I-010 1.010 I-011 0.120 I-012 0.064 I-013 0.395 I-014 0.759 I-016 0.400 I-018 0.075 I-021 0.502 I-022 1.250 I-023 0.038 I-024 0.133 I-025 0.652 I-026 0.020 I-027 0.378 I-028 0.028 I-029 0.068 I-031 0.052 I-032 0.052 I-033 0.050 I-034 0.049 I-035 0.102 I-036 0.015 I-037 0.167 I-038 0.072 I-039 0.016 I-041 0.102 I-042 0.015 I-043 0.093 I-044 0.756 I-045 0.008 I-046 0.213 I-047 0.336 I-048 0.083 I-049 0.134 I-050 0.010 I-051 0.084 I-052 0.265 I-053 0.012 I-054 0.015 I-055 0.013 I-056 0.057 I-057 0.166 I-059 0.029 I-061 0.115 I-062 0.024 I-063 0.128 I-064 1.120 I-065 0.089 I-066 1.300 I-067 0.933 I-068 0.025 I-069 1.400 I-070 0.469 I-071 0.054 I-072 0.154 I-073 0.221 I-074 0.085 I-075 0.020 I-076 0.102 I-077 0.168 I-078 0.189 I-079 1.760 I-080 1.290 I-081 0.344 I-082 3.800 I-083 0.351 I-086 0.042 I-087 0.065 I-088 0.015 I-089 0.062 I-090 0.045 I-092 0.089 I-094 0.187 I-095 1.050 I-096 0.775 I-097 0.097 I-098 0.792 I-099 0.148 I-100 0.027 I-101 0.026 I-102 0.044 I-103 4.500 I-104 0.012 I-105 0.182 I-106 0.091

(991) TABLE-US-00153 TABLE 155 Eample IC50 No. (M) I-107 0.097 I-108 0.792 I-109 0.148 I-110 0.027 I-111 0.026 I-112 0.031 I-113 0.010 I-114 0.193 I-115 0.012 I-116 0.041 I-117 0.007 I-118 0.010 I-119 0.004 I-120 0.022 I-121 0.009 I-122 0.012 I-123 0.015 I-124 0.037 I-125 0.029 I-126 0.398 I-127 0.084 I-128 0.050 I-129 0.139 I-130 0.057 I-131 0.334 I-132 0.048 I-133 0.077 I-134 0.023 I-135 0.016 I-136 0.087 I-137 0.403 I-138 0.091 I-139 0.090 I-140 0.144 I-141 0.080 I-142 0.181 I-143 0.120 I-144 0.127 I-145 0.190 I-146 0.044 I-147 0.012 I-148 0.404 I-149 0.063 I-150 0.036 I-151 0.075 I-152 0.064 I-153 0.043 I-154 0.017 I-155 0.025 I-156 0.012 I-157 0.003 I-158 0.048 I-159 0.641 I-160 0.809 I-161 0.146 I-162 0.074 I-163 0.039 I-164 0.039 I-165 0.007 I-166 0.030 I-167 0.059 I-168 0.095 I-169 0.010 I-170 0.006 I-171 0.152 I-172 0.013 I-173 0.005 I-174 0.931 I-175 0.011 I-176 0.042 I-177 0.006 I-178 0.003 I-179 0.028 I-180 0.021 I-181 0.014 I-182 0.012 I-183 0.014 I-184 0.054 I-185 0.044 I-186 0.005 I-187 0.234 I-188 0.041 I-189 0.027 I-190 0.073 I-191 0.012 I-192 0.061 I-193 0.012 I-194 0.012 I-195 0.028 I-196 0.012 I-197 0.015 I-198 0.005 I-199 0.121 I-200 0.030 I-201 0.017 I-202 0.066 I-203 0.048 I-204 0.113 I-205 0.025 I-206 0.079 I-207 0.011 I-208 0.008 I-209 0.012 I-210 0.006 I-211 0.097 I-212 0.017 I-213 0.028 I-214 0.039 I-215 0.021 I-216 0.008 I-217 0.008 I-218 0.008 I-219 0.004 I-220 0.009 I-221 0.172 I-222 0.246 I-223 0.048 I-224 0.034 I-225 0.048 I-226 0.103 I-227 0.036 I-228 0.027 I-229 0.113 I-230 0.054 I-231 0.183 I-232 0.021 I-233 0.084 I-234 0.008 I-235 0.022 I-236 0.102 I-237 0.891 I-238 0.004 I-239 0.008 I-240 0.007 I-241 0.173 I-242 0.007 I-243 0.028 I-244 0.007 I-245 0.004 I-246 0.047 I-247 0.017 I-248 0.009 I-249 0.008 I-250 0.031 I-251 0.022 I-252 0.008 I-253 0.011 I-254 0.020 I-255 0.024 I-256 0.039

(992) TABLE-US-00154 TABLE 156 I-257 0.014 I-258 0.099 I-259 0.086 I-260 0.102 I-261 0.017 I-262 0.053 I-263 0.862 I-264 0.372 I-265 0.016 I-266 0.036 I-267 0.058 I-268 0.042 I-269 0.125 I-270 0.116 I-271 0.083 I-272 0.123 I-273 0.035 I-274 0.090 I-275 0.156 I-276 0.013 I-277 0.032 I-278 0.087 I-279 0.008 I-280 0.079 I-281 0.041 I-282 0.892 I-283 0.984 I-284 0.017 I-285 0.038 I-286 0.125 I-287 0.051 I-288 0.759 I-289 0.110 I-290 0.082 I-291 0.032 I-292 0.052 I-293 0.171 I-294 0.300 I-295 0.012 I-296 0.006 I-297 0.042 I-298 0.052 I-299 0.026 I-300 0.165 I-301 0.037 I-302 0.052 I-303 0.068 I-304 0.242 I-305 0.022 I-306 0.015 I-307 0.043 I-308 0.006 I-309 0.024 I-310 0.034 I-311 0.106 I-312 0.401 I-313 0.072 I-314 0.025 I-315 0.503 I-316 0.074 I-317 0.014 I-318 0.049 I-319 0.281 I-320 0.067 I-321 0.167 I-322 0.063 I-323 0.345 I-324 0.051 I-325 0.037 I-326 0.280 I-327 0.080 I-328 0.018 I-329 0.014 I-330 0.105 I-331 0.470 I-332 0.056 I-333 0.203 I-334 0.179 I-335 0.018 I-336 0.025 I-337 0.007 I-338 0.026 I-339 0.035 I-340 0.021 I-341 0.119 I-342 0.108 I-343 0.118 I-344 0.013 I-345 0.038 I-346 0.019 I-347 0.055 I-348 0.057 I-349 0.039 I-350 0.049 I-351 0.087 I-352 0.022 I-353 0.011 I-354 0.011 I-355 0.018 I-356 0.066 I-357 0.103 I-358 0.019 I-359 0.021 I-360 0.017 I-361 0.570 I-362 0.130 I-363 0.032 I-364 0.044 I-365 0.100 I-366 0.031 I-367 0.113 I-368 0.048 I-369 0.019 I-370 0.013 I-371 0.198 I-372 0.013 I-373 0.894 I-374 0.637 I-375 0.102 I-376 0.007 I-377 0.039 I-378 0.144 I-379 0.258 I-380 0.059 I-381 0.155 I-382 0.176 I-383 0.008 I-384 0.364 I-385 0.004 I-386 0.070 I-387 0.392 I-388 0.014 I-389 0.008 I-390 0.007 I-391 0.021 I-392 0.069 I-393 0.155 I-394 0.018 I-395 0.007 I-396 0.008 I-397 0.031 I-398 0.115 I-399 0.040 I-400 0.017 I-401 0.023 I-402 0.083 I-403 0.043 I-404 0.676 I-405 0.062 I-406 0.131

(993) TABLE-US-00155 TABLE 157 I-407 0.533 I-408 0.465 I-409 0.074 I-410 0.015 I-411 0.937 I-412 0.042 I-413 0.084 I-414 0.059 I-415 0.018 I-416 0.090 I-417 0.451 I-418 0.733 I-419 0.109 I-420 0.447 I-421 0.024 I-422 0.358 I-423 0.072 I-424 0.122 I-425 0.170 I-426 0.057 I-427 0.270 I-428 0.053 I-429 0.026 I-430 0.012 I-431 0.809 I-432 0.588 I-433 0.011 I-434 0.653 I-435 0.007 I-436 0.004 I-437 0.019 I-438 0.540 I-439 0.004 I-440 0.019 I-441 0.012 I-442 0.035 I-443 0.240 I-444 0.051 I-445 0.014 I-446 0.077 I-447 0.076 I-448 0.400 I-449 0.051 I-450 0.014 I-451 0.040 I-452 0.109 I-453 0.610 I-454 0.087 I-455 0.050 I-456 0.280 I-457 0.019 I-458 0.032 I-459 0.016 I-460 0.004 I-461 0.004 I-462 0.090 I-463 0.017 I-464 0.036 I-465 0.160 I-466 0.179 I-467 0.007 I-468 0.368 I-469 0.596 I-470 0.426 I-471 0.159 I-472 0.026 I-473 0.028 I-474 0.016 I-475 0.540 I-476 0.074 I-477 0.247 I-478 0.116 I-479 0.563 I-480 0.041 I-481 0.298 I-482 0.087 I-483 0.081 I-484 0.204 I-485 0.180 I-486 0.724 I-487 0.363 I-488 0.314 I-489 0.843 I-490 0.480 I-491 0.051 I-493 0.070 I-494 0.046 I-495 0.074 I-496 0.024 I-497 0.015 I-498 0.013 I-499 0.040 I-500 0.021 I-501 0.009 I-502 0.062 I-503 0.024 I-504 0.018 I-505 0.012 I-506 0.249 I-507 0.132 I-508 0.081 I-509 0.225 I-510 0.028 I-511 0.022 I-512 0.110 I-513 0.260 I-514 0.032 I-515 0.041 I-516 0.027 I-517 0.014 I-518 0.013 I-519 0.170 I-520 0.315 I-521 0.020 I-522 0.008 I-523 0.105 I-524 0.064 I-525 0.041 I-526 0.013 I-527 0.158 I-528 0.061 I-529 0.172 I-530 0.196 I-531 0.481 I-532 0.006 I-533 0.102 I-534 0.067 I-535 0.030 I-536 0.028 I-537 0.975 I-538 0.071 I-539 0.092 I-540 0.323 I-541 0.130 I-542 0.006 I-543 0.014 I-544 0.004 I-545 0.046 I-546 0.066 I-547 0.104 I-548 0.124 I-549 0.037 I-550 0.021 I-551 0.015 I-552 0.013 I-553 0.196 I-554 0.620 I-555 0.034 I-556 0.105 I-557 0.216

(994) TABLE-US-00156 TABLE 158 I-558 0.043 I-559 0.043 I-560 0.101 I-561 0.104 I-562 0.350 I-563 0.101 I-564 0.385 I-566 0.304 I-567 0.167 I-568 0.225 I-569 0.086 I-570 0.935 I-571 0.166 I-572 0.227 I-573 0.068 I-574 0.129 I-577 0.062 I-578 0.110 I-579 0.334 I-582 0.168 I-583 0.071 I-585 0.077 I-586 0.009 I-587 0.087 I-590 0.584 I-592 0.110 I-593 0.080 I-594 0.383 I-596 0.010 I-599 0.023 I-600 0.013 I-601 0.008 I-602 0.012 I-603 0.007 I-604 0.006 I-605 0.013 I-606 0.074 I-607 0.110 I-608 0.011 I-609 0.525 I-610 0.085 I-611 0.003 I-614 0.011 I-615 0.027 I-616 0.240 I-617 0.009 I-618 0.017 I-619 0.009 I-620 0.028 I-621 0.008 I-622 0.072 I-623 0.017 I-624 0.009 I-625 0.005 I-626 0.006 I-627 0.005 I-628 0.059 I-629 0.098 I-630 0.025 I-631 0.010 I-632 0.019 I-634 0.034 I-635 0.104 I-636 0.004 I-637 0.004 I-638 0.140 I-639 0.002 I-640 0.110 I-641 0.073 I-642 0.007 I-643 0.250 I-644 0.026 I-646 0.015 I-647 0.006 I-648 0.110 I-649 0.009 I-650 0.375 I-651 0.004 I-652 0.007 I-653 0.065 I-655 0.002 I-656 0.039 I-657 0.014 I-658 0.004 I-659 0.023 I-661 0.457 I-662 0.005 I-663 0.700 I-664 0.011 I-665 0.004 I-666 0.298 I-667 0.008 I-668 0.007 I-669 0.620 I-670 0.011 I-671 0.011 I-672 0.030 I-673 0.650 I-674 0.007 I-675 0.018 I-677 0.013 I-678 0.123 I-679 0.625 I-680 0.140 I-682 0.005 I-683 0.003 I-684 0.006 I-685 0.170 I-686 0.005 I-687 0.014 I-688 0.004 I-689 0.025 I-691 0.025 I-692 0.034 I-693 0.008 I-694 0.013 I-695 0.096 I-696 0.497 I-697 0.004 I-698 0.003 I-700 0.009 I-701 0.023 I-702 0.015 I-703 0.030 I-705 0.009 I-706 0.048 I-707 0.084 I-708 0.005 I-709 0.133 I-710 0.006 I-711 0.007 I-713 0.003 I-714 0.044 I-716 0.170 I-717 0.015 I-720 0.775 I-722 0.009 I-723 0.041 I-724 0.009 I-725 0.101 I-726 0.009 I-727 0.194 I-728 0.008 I-729 0.004 I-730 0.910 I-732 0.260 I-733 0.009 I-734 0.004 I-735 0.677 I-736 0.087

(995) TABLE-US-00157 TABLE 159 I-737 0.033 I-738 0.035 I-739 0.007 I-740 0.003 I-741 0.007 I-742 0.013 I-744 0.740 I-745 0.490 I-746 0.350 I-747 0.044 I-748 0.005

Test Example 2

CYP Inhibition Test

(996) Using commercially available human hepatic microsome, and employing, as markers, 7-ethoxyresorufin O-deethylation (CYP1A2), tolbutamide methyl-hydroxylation (CYP2C9), mephenytoin 4-hydroxylation (CYP2C19), dextromethorphan 0-demethylation (CYP2D6), and terfenedine hydroxylation atypical substrate metabolism reactions of human main five CYP enzyme forms (CYP1A2, 2C9, 2C19, 2D6, 3A4), an inhibitory degree of each metabolite production amount by a test compound was assessed.

(997) The reaction conditions were as follows: substrate, 0.5 mol/L ethoxyresorufin (CYP1A2), 100 mol/L tolbutamide (CYP2C9), 50 mol/L S-mephenitoin (CYP2C19), 5 mmol/L dextromethorphan (CYP2D6), 1 mol/L terfenedine (CYP3A4); reaction time, 15 minutes; reaction temperature, 37 C.; enzyme, pooled human hepatic microsome 0.2 mg protein/mL; test drug concentration, 1, 5, 10, 20 mol/L (four points).

(998) Each five kinds of substrates, human hepatic microsome, or a test drug in 50 mM Hepes buffer as a reaction solution was added to a 96-well plate at the composition as described above, NADPH, as a cofactor was added to initiate metabolism reactions as markers and, after the incubation at 37 C. for 15 minutes, a methanol/acetonitrile=1/1 (v/v) solution was added to stop the reaction. After the centrifugation at 3000 rpm for 15 minutes, resorufin (CYP1A2 metabolite) in the supernatant was quantified by a fluorescent multilabel counter and tributamide hydroxide (CYP2CP metabolite), mephenytoin 4 hydroxide (CYP2C19 metabolite), dextromethorphan (CYP2D6 metabolite), and terfenadine alcohol (CYP3A4 metabolite) are quantified by LC/MS/MS.

(999) Addition of only DMSO being a solvent dissolving a drug to a reaction system was adopted as a control (100%), remaining activity (%) was calculated at each concentration of a test drug added as the solution and IC50 was calculated by reverse presumption by a logistic model using a concentration and an inhibition rate.

Test Example 3

BA Test

(1000) An experimental material and a method for examining oral absorbability (1) Animals used: SD rats or mice were used (2) Breeding condition: chow and sterilized tap water were allowed to be taken in freely. (3) Setting of a dosage and grouping: a predetermined dosage was administered orally or intravenously. Groups were formed as shown below. (A dosage varied depending on each compound) Oral administration 1-30 mg/kg (n=2 to 3) Intravenous administration 0.5-10 mg/kg (n=2 to 3) (4) Preparation of administered liquid: In oral administration, a solution or suspension was administered. In intravenous administration, after solubilization, the administration was performed. (5) Method of Administration: In oral administration, compulsory administration to the stomach was conducted using an oral probe. In intravenous administration, administration from the caudal vein was conducted using a syringe with an injection needle. (6) Evaluation item: Blood was chronologically collected, and then the concentration of a compound of the present invention in blood plasma was measured using a LC/MS/MS. (7) Statistical analysis: With regard to a shift in plasma concentration, the plasma concentration-time area under the curve (AUC) was calculated using a nonlinear least-squares program WinNonlin Bioavailability (BA) was calculated from the AUCs of the oral administration group and the intravenous administration group, respectively.

Test Example 4

Metabolism Stability Test

(1001) Using commercially available pooled human hepatic microsomes, a test compound was reacted for a constant time, a remaining rate was calculated by comparing a reacted sample and an unreacted sample, thereby, a degree of metabolism in liver was assessed.

(1002) A reaction was performed (oxidative reaction) at 37 C. for 0 minute or 30 minutes in the presence of 1 mmol/L NADPH in 0.2 mL of a buffer (50 mmol/L Tris-HCl pH 7.4, 150 mmol/L potassium chloride, 10 mol/L magnesium chloride) containing 0.5 mg protein/mL of human liver microsomes. After the reaction, 50 L of the reaction solution was added to 100 L of a methanol/acetonitrile=1/1 (v/v), mixed and centrifuged at 3000 rpm for 15 minutes. The test compound in the supernatant was quantified by LC/MS/MS, and a remaining amount of the test compound after the reaction was calculated, letting a compound amount at 0 minute reaction time to be 100%. Hydrolysis reaction was performed in the absence of NADPH and glucuronidation reaction was in the presence of 5 mM UDP-glucuronic acid in place of NADPH, followed by similar operations.

Test Example 5

CYP3A4 Fluorescent MBI Test

(1003) The CYP3A4 fluorescent MBI test is a test of investigating enhancement of CYP3A4 inhibition of a compound by a metabolism reaction, and the test was performed using, a reaction in which 7-benzyloxytrifluoromethylcoumarin (7-BFC) was debenzylated by the CYP3A4 enzyme to produce a metabolite, 7-hydroxytrifluoromethylcoumarin (HFC) emitting fluorescent light.

(1004) The reaction conditions were as follows: substrate, 5.6 mol/L 7-BFC; pre-reaction time, 0 or 30 minutes; reaction time, 15 minutes; reaction temperature, 25 C. (room temperature); CYP3A4 content (expressed in Escherichia coli), at pre-reaction 62.5 mol/mL, at reaction 6.25 mol/mL (at 10-fold dilution); test drug concentration, 0.625, 1.25, 2.5, 5, 10, 20 mol/L (six points).

(1005) An enzyme in a K-Pi buffer (pH 7.4) and a test drug solution as a pre-reaction solution were added to a 96-well plate at the composition of the pre-reaction, a part of it was transferred to another 96-well plate so that it was 1/10 diluted by a substrate in a K-Pi buffer, NADPH as a co-factor was added to initiate a reaction as an index (without preincubation) and, after a predetermined time of a reaction, acetonitrile/0.5 mol/L Tris (trishydroxyaminomethane)=4/1 was added to stop the reaction. In addition, NADPH was added to a remaining preincubation solution to initiate a preincubation (with preincubation) and, after a predetermined time of a preincubation, a part was transferred to another plate so that it was 1/10 diluted with a substrate and a K-Pi buffer to initiate a reaction as an index. After a predetermined time of a reaction, acetonitrile/0.5 mol/L Tris (trishydroxyaminomethane)=4/1 was added to stop the reaction. For the plate on which each index reaction had been performed, a fluorescent value of 7-HFC which is a metabolite was measured with a fluorescent plate reader. (Ex=420 nm, Em=535 nm).

(1006) Addition of only DMSO which was a solvent dissolving a drug to a reaction system was adopted as a control (100%), remaining activity (%) was calculated at each concentration of a test drug added as the solution, and IC50 was calculated by reverse-presumption by a logistic model using a concentration and an inhibition rate. When a difference between IC50 values was 5 M or more, this was defined as (+) and, when the difference was 3 M or less, this was defined as ().

Test Example 6

Fluctuation Ames Test

(1007) The compounds of the present invention are assessed for mutagenic property.

(1008) 20 L of freezing-stored rat typhoid bacillus (Salmonella typhimurium TA98 strain, TA100 strain) is inoculated on 10 mL of a liquid nutrient medium (2.5% Oxoid nutrient broth No. 2), and this is cultured before shaking at 37 C. for 10 hours. 9 mL of a bacterial solution of the TA98 strain is centrifuged (2000 g, 10 minutes) to remove a culturing solution, the bacteria is suspended in 9 mL of a Micro F buffer (K2HPO4: 3.5 g/L, KH2PO4: 1 g/L, (NH4)2SO4: 1 g/L, trisodium citrate dehydrate: 0.25 g/L, MgSO4.7H2O: 0.1 g/L), the suspension is added to 110 mL of an Exposure medium (Micro F buffer containing Biotin: 8 g/mL, histidine: 0.2 g/mL, glucose: 8 mg/mL), and the TA100 strain is added to 120 mL of the Exposure medium relative to 3.16 mL of the bacterial solution to prepare a test bacterial solution. Each 12 mL of a test substance DMSO solution (8 stage dilution from maximum dose 50 mg/mL at 2-fold ratio), DMSO as a negative control, 50 g/mL of 4-nitroquinoline-1-oxide DMSO solution for the TA98 strain, 0.25 g/mL of 2-(2-furyl)-3-(5-nitro-2-furyl)acrylamide DMSO solution for the TA100 strain under the non-metabolism activating condition, 40 g/mL of 2-aminoanthracene DMSO solution for the TA98 strain, 20 g/mL of 2-aminoanthracene DMSO solution for the TA100 strain under the metabolism activating condition as a positive control, and 588 L of the test bacterial solution (a mixed solution of 498 l of the test bacterial solution and 90 L of S9 mix under the metabolism activating condition) are mixed, and this is shaking-cultured at 37 C. for 90 minutes. 460 L of the bacterial solution exposed to the test substance is mixed with 2300 L of an Indicator medium (Micro F buffer containing biotin: 8 g/mL, histidine: 0.2 g/mL, glucose: 8 g/mL, Bromo Cresol Purple: 37.5 g/mL), each 50 L is dispensed into microplate 48 wells/dose, and this is subjected to stationary culturing at 37 C. for 3 days. Since a well containing a bacterium which has obtained the proliferation ability by mutation of an amino acid (histidine) synthesizing enzyme gene turns from purple to yellow due to a pH change, the bacterium proliferation well which has turned to yellow in 48 wells per dose is counted, and is assessed by comparing with a negative control group. 0 means that mutagenicity is negative and (+) is positive.

Test Example 7

hERG Test

(1009) For the purpose of assessing risk of an electrocardiogram QT interval prolongation, effects on delayed rectifier K+ current (IKr), which plays an important role in the ventricular repolarization process of the compound of the present invention, was studied using HEK293 cells expressing human ether-a-go-go related gene (hERG) channel.

(1010) After a cell was retained at a membrane potential of 80 mV by whole cell patch clamp method using an automated patch clamp system (PatchXpress 7000A, Axon Instruments Inc.), IKr induced by depolarization pulse stimulation at +40 mV for 2 seconds and, further, repolarization pulse stimulation at 50 mV for 2 seconds is recorded. After the generated current was stabilized, extracellular solution (NaCl: 135 mmol/L, KCl: 5.4 mmol/L, NaH.sub.2PO.sub.4: 0.3 mmol/L, CaCl.sub.2.2H2O: 1.8 mmol/L, MgCl.sub.2. 6H2O: 1 mmol/L, glucose: 10 mmol/L, HEPES (4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid): 10 mmol/L, pH=7.4) in which the test compound has been dissolved at an objective concentration is applied to the cell under the room temperature condition for 10 minutes. From the recording IKr, an absolute value of the tail peak current was measured based on the current value at the resting membrane potential using an analysis software (DataXpress ver. 1, Molecular Devices Corporation). Further, the % inhibition relative to the tail peak current before application of the test substance was calculated, and compared with the vehicle-applied group (0.1% dimethyl sulfoxide solution) to assess influence of the test substance on IKr.

Test Example 8

Solubility Test

(1011) The solubility of the compounds of the present invention was determined in 1% DMSO addition condition. The 10 mmol/L compound solution was prepared in DMSO, To the pH6.8 artificial intestinal fluid (To 0.2 mol/L potassium dihydrogen phosphate reagent 250 mL and 0.2 mol/L NaOH reagent solution, water was added until it become 1000 mL solution) 594 L, the compound of the present invention solution 6 L was added. After stood at 25 C. for 16 hours, the mixture was filtered while suctioning. The filtrate was diluted two-fold with methanol/water=1/1(V/V), and its concentration into the filtrate was measured by the absolute calibration curve method using HPLC or LC/MS/MS.

Test Example 9

Powder Solubility Test

(1012) Appropriate amounts of the test substances were put into appropriate containers. To the respective containers were added 200 L of JP-1 fluid (sodium chloride 2.0 g, hydrochloric acid 7.0 mL and water to reach 1000 mL), 200 L of JP-2 fluid (phosphate buffer (pH6.8) 500 mL and water 500 mL), and 200 L of 20 mmol/L TCA (sodium taurocholate)/JP-2 fluid (TCA 1.08 g and water to reach 100 mL). In the case that the test compound was dissolved after the addition of the test fluid, the bulk powder was added as appropriate. The containers were sealed, and shaken for 1 hour at 37 C. The mixtures are filtered, and 100 L of methanol was added to each of the filtrate (100 L) so that the filtrates were two-fold diluted. The dilution ratio was changed if necessary. The dilutions were observed for bubbles and precipitates, and then the containers were sealed and shaken. Quantification was performed by HPLC with an absolute calibration method.

Formulation Example

(1013) The following Formulation Examples are only exemplified and not intended to limit the scope of this invention.

Formulation Example 1

Tablets

(1014) TABLE-US-00158 The compound of the present invention 15 mg Lactose 15 mg Calcium stearate 3 mg

(1015) The components other than calcium stearate are homogeneously mixed and dried by crushing granulation, and appropriate size granules. Then the tablets are compression-molded by the addition of calcium stearate.

Formulation Example 2

Capsules

(1016) TABLE-US-00159 The compound of the present invention 10 mg Magnesium sterate 10 mg Lactose 80 mg

(1017) They are uniformly mixed to produce a powder medicine as a powder or fine granules. The capsule are made by filling them into a capsule container

Formulation Example 3

Granules

(1018) TABLE-US-00160 The compound of the present invention 30 g Lactose 265 g Magnesium stearate 5 g

(1019) After the above ingredients are mixed uniformly, the mixture is compressed, crushed, granulated and sieved to obtain a suitable size of granules.

INDUSTRIAL APPLICABILITY

(1020) The compounds of this invention have an ACC2 inhibitory activity, and are very useful for treatment or prevention of a disease associated with ACC2.