Sulfonamide derivative and pharmaceutically acceptable acid addition salt thereof

Abstract

The present invention aims to provide a novel low-molecular-weight compound exhibiting an orexin receptor agonist activity and expected to be useful as a prophylactic or therapeutic agent for narcolepsy and the like. The present invention provides a compound represented by the formula (I): ##STR00001##
wherein each symbol is as defined in the description, or a pharmaceutically acceptable acid addition salt thereof, which has an orexin receptor agonist activity, and an orexin receptor agonist containing the compound or a pharmaceutically acceptable acid addition salt thereof.

Claims

1. A compound represented by the formula (I): ##STR00268## wherein R.sup.1 is a hydrogen atom, C.sub.1-6 alkoxy, OH, C.sub.1-6 alkyl or a halogen atom, X is C(R.sup.5) or N, R.sup.5 is a hydrogen atom or C.sub.1-6 alkoxy, any one of R.sup.2, R.sup.3 and R.sup.4 is R.sup.6 and the remaining two are each a hydrogen atom, R.sup.6 is (1) NR.sup.17Y.sup.1R.sup.7 wherein Y.sup.1 is C(O)NR.sup.18, C(S)NH, C(NH)NH, C(O)O, C(O), SO.sub.2 or SO.sub.2NR.sup.8, R.sup.8 is a hydrogen atom or C.sub.1-6 alkyl, R.sup.17 is a hydrogen atom or C.sub.1-6 alkyl, R.sup.18 is a hydrogen atom or C.sub.1-6 alkyl, or R.sup.17 and R.sup.18 are optionally bonded to each other to form, together with the nitrogen atoms bonded thereto and adjacent C(O), a 5- to 7-membered heterocycle, R.sup.7 is (a) C.sub.6-10 aryl, (b) 5- to 10-membered heteroaryl, (c) C.sub.1-6 alkyl, or (d) C.sub.2-6 alkenyl wherein C.sub.1-6 alkyl and C.sub.2-6 alkenyl are optionally substituted by one substituent selected from phenyl, furyl and diphenylmethylsulfinyl, C.sub.6-10 aryl and 5- to 10-membered heteroaryl are optionally substituted by optionally selected R.sup.9 in the number of 1 to 4, R.sup.9 are each independently a halogen atom, NO.sub.2, OH, C.sub.1-6 alkyl, C.sub.1-6 haloalkyl, C.sub.1-6 alkoxy, 5- to 10-membered heteroaryl, NR.sup.9aR.sup.9b wherein R.sup.9a is a hydrogen atom, C.sub.1-6 alkyl or C.sub.1-6 alkoxy-carbonyl, and R.sup.9b is a hydrogen atom or C.sub.1-6 alkyl, C(O)OR.sup.9c wherein R.sup.9c is a hydrogen atom or C.sub.1-6 alkyl, C(O)NR.sup.9dR.sup.9e wherein R.sup.9d is a hydrogen atom or C.sub.1-6 alkyl, and R.sup.9e is a hydrogen atom or C.sub.1-6 alkyl, or NHC(NR.sup.9f)NHR.sup.9g wherein R.sup.9f is a hydrogen atom or C.sub.1-6 alkoxy-carbonyl, and R.sup.9g is a hydrogen atom or C.sub.1-6 alkoxy-carbonyl, or R.sup.9 in the number of 2 are joined to form methylenedioxy, (2) NHY.sup.2R.sup.10 wherein Y.sup.2 is CH.sub.2 or a single bond, and R.sup.10 is (a) C.sub.6-10 aryl, or (b) 5- to 10-membered heteroaryl wherein C.sub.6-10 aryl and 5- to 10-membered heteroaryl are optionally substituted by optionally selected R.sup.9 in the number of 1 to 4, and R.sup.9 is as defined above, (3) a group represented by the formula (ii): ##STR00269## wherein R.sup.11 is C.sub.1-6 alkoxy or C.sub.6-10 arylamino (wherein C.sub.6-10 aryl moiety of the C.sub.6-10 arylamino is optionally substituted by 1 to 3 substituents selected from C.sub.1-6 alkyl and C.sub.1-6 alkoxy), (4) NNR.sup.12 wherein R.sup.12 is C.sub.6-10 aryl optionally substituted by 1 to 3 substituents selected from (a) C.sub.1-6 alkyl optionally substituted by OH, (b) OH, (c) di(C.sub.1-6 alkyl)amino and (d) C.sub.1-6 alkoxy-carbonylamino, or (5) NR.sup.13R.sup.14 wherein R.sup.13 is a hydrogen atom, C.sub.1-6 alkyl, C.sub.6-10 aryl-C.sub.1-6 alkyl or C.sub.2-6 alkenyl-carbonyl, and R.sup.14 is a hydrogen atom or C.sub.1-6 alkyl (wherein C.sub.1-6 alkyl is optionally substituted by one substituent selected from (a) C.sub.2-6 alkenyl-carbonylamino and (b) C.sub.6-10 aryl-C.sub.1-6 alkylaminocarbonyl optionally substituted by C.sub.1-6 alkyl), or R.sup.13 and R.sup.14 are bonded to each other to form, together with the nitrogen atom bonded thereto, a 5- to 7-membered heterocycle further containing one nitrogen atom (wherein 5- to 7-membered heterocycle is optionally substituted by C.sub.6-10 aryl-carbonyl optionally substituted by C.sub.1-6 alkyl), provided that when R.sup.14 is ethyl substituted by C.sub.2-6 alkenyl-carbonylamino, R.sup.13 is not a hydrogen atom, and W is a group represented by the formula (iii): ##STR00270## wherein R.sup.15 is C.sub.1-6 alkyl, and R.sup.16 is C.sub.1-6 alkyl, or a pharmaceutically acceptable acid addition salt thereof.

2. The compound according to claim 1 wherein R.sup.17 and R.sup.18 are each a hydrogen atom, or a pharmaceutically acceptable acid addition salt thereof.

3. The compound according to claim 1 wherein X is C(R.sup.5), wherein R.sup.5 is a hydrogen atom or C.sub.1-6 alkoxy, or a pharmaceutically acceptable acid addition salt thereof.

4. The compound according to claim 1 wherein R.sup.2 is R.sup.6 (wherein R.sup.6 is as defined in claim 1), and R.sup.3 and R.sup.4 are each a hydrogen atom, or a pharmaceutically acceptable acid addition salt thereof.

5. The compound according to claim 1 wherein R.sup.6 is NR.sup.17Y.sup.1R.sup.7 (wherein R.sup.17, Y.sup.1 and R.sup.7 are as defined in claim 1), or a pharmaceutically acceptable acid addition salt thereof.

6. The compound according to claim 1 wherein R.sup.6 is NHY.sup.2R.sup.10 (wherein Y.sup.2 and R.sup.10 are as defined in claim 1), or a pharmaceutically acceptable acid addition salt thereof.

7. The compound according to claim 1 wherein R.sup.6 is a group represented by the formula (ii): ##STR00271## wherein R.sup.11 is as defined in claim 1, or a pharmaceutically acceptable acid addition salt thereof.

8. The compound according to claim 1 wherein R.sup.6 is NNR.sup.12 (wherein R.sup.12 is as defined in claim 1), or a pharmaceutically acceptable acid addition salt thereof.

9. The compound according to claim 1 wherein R.sup.6 is NR.sup.13R.sup.14 (wherein R.sup.13 and R.sup.14 are as defined in claim 1), or a pharmaceutically acceptable acid addition salt thereof.

10. The compound according to claim 1 wherein W is a group represented by the formula (iii): ##STR00272## wherein R.sup.15 is C.sub.1-6 alkyl and R.sup.16 is C.sub.1-6 alkyl, X is C(R.sup.5) wherein R.sup.5 is a hydrogen atom or C.sub.1-6 alkoxy, R.sup.2 is NHY.sup.1R.sup.7 wherein Y.sup.1 and R.sup.7 are as defined in claim 1, and R.sup.3 and R.sup.4 are each a hydrogen atom, or a pharmaceutically acceptable acid addition salt thereof.

11. The compound according to claim 10 wherein Y.sup.1 is C(O)NH, C(S)NH, C(NH)NH or C(O)O, or a pharmaceutically acceptable acid addition salt thereof.

12. A compound represented by the formula (I-B): ##STR00273## wherein R.sup.7a is phenyl substituted by NR.sup.9aR.sup.9b (wherein R.sup.9a is C.sub.1-6 alkyl and R.sup.9b is C.sub.1-6 alkyl), R.sup.1 is a hydrogen atom, C.sub.1-6 alkoxy, OH, C.sub.1-6 alkyl or a halogen atom, R.sup.Wa is C.sub.1-6 alkyl (wherein C.sub.1-6 alkyl is optionally substituted by phenyl, pyridyl, C.sub.1-6 alkoxy-carbonylamino or di(C.sub.1-6 alkyl)amino) or phenyl (wherein phenyl is optionally substituted by di(C.sub.1-6 alkyl)amino), and R.sup.Wb is a hydrogen atom or C.sub.1-6 alkyl, or a pharmaceutically acceptable acid addition salt thereof.

13. A compound represented by the formula (I): ##STR00274## wherein R.sup.1 is a hydrogen atom, C.sub.1-6 alkoxy, OH, C.sub.1-6 alkyl or a halogen atom, X is C(R.sup.5) or N, R.sup.5 is a hydrogen atom or C.sub.1-6 alkoxy, R.sup.6a is an optionally substituted hydrocarbon group, an optionally substituted heterocyclic group, a group bonded via an oxygen atom, or a group bonded via a sulfur atom, R.sup.15 is C.sub.1-6 alkyl, and R.sup.16 is C.sub.1-6 alkyl, or a pharmaceutically acceptable acid addition salt thereof.

14. A medicament comprising the compound according to claim 1 or a pharmaceutically acceptable acid addition salt thereof.

15. A method of treating or preventing narcolepsy narcolepsy, obesity, diabetes, depression, sepsis, severe sepsis or septic shock comprising administering an effective amount of the compound according to claim 1 or a pharmaceutically acceptable acid addition salt thereof.

16. A method of improving sleepiness comprising administering an effective amount of the compound according to claim 1 or a pharmaceutically acceptable acid addition salt thereof.

17. A medicament comprising the compound according to claim 13 or a pharmaceutically acceptable acid addition salt thereof.

18. A method of treating or preventing narcolepsy, obesity, diabetes, depression, sepsis, severe sepsis or septic shock, or improving sleepiness comprising administering an effective amount of the compound according to claim 13 or a pharmaceutically acceptable acid addition salt thereof.

19. A medicament comprising the compound according to claim 12 or a pharmaceutically acceptable acid addition salt thereof.

20. A method of treating or preventing narcolepsy, obesity, diabetes, depression, sepsis, severe sepsis or septic shock, or improving sleepiness comprising administering an effective amount of the compound according to claim 12 or a pharmaceutically acceptable acid addition salt thereof.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) The FIGURE shows a hypnogram for 3 hr after intraventricular administration of a control substance (5% chromophore-containing saline (Vehicle)) or a test compound (compound of Example 40) to a wild-type mouse (WT mouse) in light period.

DESCRIPTION OF EMBODIMENTS

(2) The following terms used in the present specification are as defined below unless otherwise specified.

(3) The C.sub.1-6 alkyl in the present specification means a monovalent straight chain or branched saturated hydrocarbon group having a carbon number of 1 to 6 and composed of a carbon atom and a hydrogen atom. For example, methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, neopentyl, hexyl and the like can be mentioned.

(4) The C.sub.1-6 alkoxy in the present specification means an oxy group to which C.sub.1-6 alkyl is bonded. For example, methoxy, ethoxy, propoxy, isopropoxy, butoxy, isobutoxy, tert-butoxy and the like can be mentioned.

(5) The halogen atom in the present specification means a fluorine atom, a chlorine atom, a bromine atom or an iodine atom.

(6) The C.sub.2-6 alkenyl in the present specification means a monovalent straight chain or branched unsaturated hydrocarbon group having a carbon number of 2 to 6 and at least one double bond, and composed of a carbon atom and a hydrogen atom. For example, ethenyl, 1-propenyl, 2-propenyl, 2-methyl-1-propenyl, 1-butenyl, 2-butenyl, 3-butenyl, 3-methyl-2-butenyl, 1-pentenyl, 2-pentenyl, 3-pentenyl, 4-pentenyl, 4-methyl-3-pentenyl, 1-hexenyl, 3-hexenyl, 5-hexenyl and the like can be mentioned.

(7) The C.sub.2-6 alkynyl in the present specification means a monovalent straight chain or branched unsaturated hydrocarbon group having a carbon number of 2 to 6 and at least one triple bond, and composed of a carbon atom and a hydrogen atom. For example, ethynyl, propynyl, butynyl, pentynyl, hexynyl and the like can be mentioned.

(8) The C.sub.3-10 cycloalkyl in the present specification means a monocyclic or polycyclic aliphatic carbon cyclic group having 3 to 10 carbon atoms. For example, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, adamantyl and the like can be mentioned.

(9) The C.sub.6-10 aryl in the present specification means a monocyclic or fused aromatic carbon cyclic group having 6 to 10 carbon atoms. For example, phenyl, 1-naphthyl, 2-naphthyl and the like can be mentioned.

(10) The 5- to 10-membered heteroaryl in the present specification means a 5- to 10-membered monocyclic or bicyclic aromatic heterocyclic group containing, as a ring-constituting atom besides carbon atom, 1 to 4 hetero atoms of one or two kinds selected from oxygen atom, sulfur atom and nitrogen atom. For example, thienyl, furyl, pyrrolyl, imidazolyl, pyrazolyl, triazolyl, tetrazolyl, oxazolyl, isoxazolyl, triazolyl, isothiazolyl, pyridyl, pyridazinyl, pyrimidinyl, furazanyl, pyrazinyl, thiadiazolyl, oxadiazolyl, benzofuryl, benzothienyl, benzimidazolyl, benzothiazolyl, quinolyl, isoquinolyl, cinnolinyl, quinazolinyl, quinoxalinyl, phthalazinyl, 1H-indazolyl and the like can be mentioned.

(11) The C.sub.1-6 haloalkyl in the present specification means a C.sub.1-6 alkyl substituted by 1 to 5 (preferably 1 to 3) halogen atoms. For example, trifluoromethyl, 2,2,2-trifluoroethyl, 3,3,3-trifluoropropyl and the like can be mentioned. It is preferably trifluoromethyl.

(12) The C.sub.1-6 alkoxy-carbonyl in the present specification means a carbonyl group bonded to C.sub.1-6 alkoxy. For example, methoxycarbonyl, ethoxycarbonyl, propoxycarbonyl, isopropoxycarbonyl, butoxycarbonyl, isobutoxycarbonyl, tert-butoxycarbonyl and the like can be mentioned.

(13) The C.sub.6-10 arylamino in the present specification means an amino substituted by C.sub.6-10 aryl. For example, phenylamino, 1-naphthylamino, 2-naphthylamino and the like can be mentioned. It is preferably phenylamino.

(14) The C.sub.1-6 alkyl optionally substituted by OH in the present specification means C.sub.1-6 alkyl optionally substituted by one OH. For example, hydroxymethyl, 2-hydroxyethyl, 3-hydroxypropyl and the like can be mentioned.

(15) The di(C.sub.1-6 alkylamino in the present specification means an amino substituted by two C.sub.1-6 alkyl. For example, dimethylamino, diethylamino, dipropylamino, diisopropylamino, N-ethyl-N-methylamino and the like can be mentioned.

(16) The C.sub.1-6 alkoxy-carbonylamino in the present specification means an amino substituted by C.sub.1-6 alkoxy-carbonyl. For example, methoxycarbonylamino, ethoxycarbonylamino, propoxycarbonylamino, isopropoxycarbonylamino, butoxycarbonylamino, isobutoxycarbonylamino, tert-butoxycarbonylamino and the like can be mentioned.

(17) The C.sub.6-10 aryl-C.sub.1-6 alkyl in the present specification means C.sub.1-6 alkyl substituted by C.sub.6-10 aryl. For example, benzyl, phenethyl and the like can be mentioned. It is preferably, benzyl.

(18) The C.sub.2-6 alkenyl-carbonyl in the present specification means a carbonyl group bonded to C.sub.2-6 alkenyl. For example, acryloyl, methacryloyl and the like can be mentioned.

(19) The C.sub.2-6 alkenyl-carbonylamino in the present specification means an amino substituted by C.sub.2-6 alkenyl-carbonyl. For example, acryloylamino, methacryloylamino and the like can be mentioned.

(20) The C.sub.6-10 aryl-C.sub.1-6 alkylaminocarbonyl in the present specification means an aminocarbonyl substituted by C.sub.6-10 aryl-C.sub.1-6 alkyl. For example, benzylaminocarbonyl, phenethylaminocarbonyl and the like can be mentioned. It is preferably benzylaminocarbonyl.

(21) The C.sub.6-10 aryl-carbonyl in the present specification means a carbonyl group bonded to C.sub.6-10 aryl. For example, benzoyl, 1-naphthoyl, 2-naphthoyl and the like can be mentioned. It is preferably benzoyl.

(22) In the present specification, as the 5- to 7-membered heterocycle further containing one nitrogen atom, which is formed by R.sup.13 and R.sup.14, bonded to each other, together with the nitrogen atom bonded thereto, imidazolidine, piperazine or 1,4-diazepane can be mentioned.

(23) In the present specification, as the 5- to 7-membered heterocycle formed by R.sup.17 and R.sup.18, bonded to each other, together with the nitrogen atoms bonded thereto and adjacent C(O), imidazolidin-2-one, hexahydropyrimidin-2-one or 1,3-diazepan-2-one can be mentioned.

(24) As the hydrocarbon group of the optionally substituted hydrocarbon group in the present specification, C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.2-6 alkynyl, C.sub.3-10 cycloalkyl, C.sub.6-10 aryl and the like can be mentioned.

(25) As the heterocyclic group of the optionally substituted heterocyclic group in the present specification, 5- to 10-membered heteroaryl, 4- to 10-membered nonaromatic heterocyclic group and the like can be mentioned.

(26) The 4- to 10-membered nonaromatic heterocyclic group in the present specification means a 4- to 10-membered monocyclic or bicyclic saturated or unsaturated nonaromatic heterocyclic group containing, as a ring-constituting atom besides carbon atom, 1 to 4 hetero atoms of one or two kinds selected from oxygen atom, sulfur atom and nitrogen atom. For example, azetidinyl, oxetanyl, pyrrolidinyl, tetrahydrofuryl, imidazolidinyl, pyrazolidinyl, piperidyl, tetrahydropyranyl, tetrahydrothiopyranyl, piperazinyl, morpholinyl, thiomorpholinyl, azepanyl, oxazepanyl, diazepanyl, pyrrolinyl, imidazolinyl, pyrazolinyl and the like can be mentioned.

(27) As the group bonded via an oxygen atom in the present specification, an oxy group (O) bonded to an optionally substituted hydrocarbon group or optionally substituted heterocyclic group and the like can be mentioned.

(28) As the group bonded via a sulfur atom in the present specification, a thio group (S), sulfinyl group (SO) or sulfonyl group (SO.sub.2) bonded to an optionally substituted hydrocarbon group, an optionally substituted heterocyclic group, or a group bonded via a nitrogen atom and the like can be mentioned.

(29) As the group bonded via a nitrogen atom in the present specification, amino bonded to an optionally substituted hydrocarbon group, amino bonded to an optionally substituted heterocyclic group and the like can be mentioned.

(30) Being optionally substituted in the present specification means, for example, being optionally substituted by 1 to 5, preferably 1 to 3, substituents selected from the following substituent group.

(31) Substituent Group halogen atom, NO.sub.2, CN, OH, oxo (O), C.sub.1-6 alkyl, C.sub.1-6 haloalkyl, C.sub.1-6 alkoxy, C.sub.2-6 alkenyl, C.sub.2-6 alkynyl, C.sub.3-10 cycloalkyl, C.sub.6-10 aryl, C.sub.6-10 aryl-C.sub.1-6 alkyl, 5- to 10-membered heteroaryl, 4- to 10-membered nonaromatic heterocyclic group, NR.sup.21aR.sup.21b wherein R.sup.21a and R.sup.21b are each independently a hydrogen atom, C.sub.1-6 alkyl, C.sub.1-6 alkoxy-carbonyl, C.sub.2-6 alkenyl, C.sub.2-6 alkynyl, C.sub.3-10 cycloalkyl, C.sub.6-10 aryl, C.sub.6-10 aryl-C.sub.1-6 alkyl, 5- to 10-membered heteroaryl or 4- to 10-membered nonaromatic heterocyclic group, C(O)OR.sup.21c wherein R.sup.21c is a hydrogen atom, C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.2-6 alkynyl, C.sub.3-10 cycloalkyl, C.sub.6-10 aryl or C.sub.6-10 aryl-C.sub.1-6 alkyl, C(O)NR.sup.21dR.sup.21e wherein R.sup.21d and R.sup.21e are each independently a hydrogen atom, C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.2-6 alkynyl, C.sub.3-10 cycloalkyl, C.sub.6-10 aryl, C.sub.6-10 aryl-C.sub.1-6 alkyl, 5- to 10-membered heteroaryl or 4- to 10-membered nonaromatic heterocyclic group, NHC(NR.sup.21f)NHR.sup.21g wherein R.sup.21f is a hydrogen atom or C.sub.1-6 alkoxy-carbonyl and R.sup.21g is a hydrogen atom or C.sub.1-6 alkoxy-carbonyl, OR.sup.21h wherein R.sup.21h is C.sub.1-6 haloalkyl, C.sub.2-6 alkenyl, C.sub.2-6 alkynyl, C.sub.3-10 cycloalkyl, C.sub.6-10 aryl, C.sub.6-10 aryl-C.sub.1-6 alkyl, 5- to 10-membered heteroaryl or 4- to 10-membered nonaromatic heterocyclic group, C(O)R.sup.21i wherein R.sup.21i is a hydrogen atom, C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.2-6 alkynyl, C.sub.3-10 cycloalkyl, C.sub.6-10 aryl, C.sub.6-10 aryl-C.sub.1-6 alkyl, 5- to 10-membered heteroaryl or 4- to 10-membered nonaromatic heterocyclic group, NR.sup.21j wherein R.sup.21j is a hydrogen atom, OH or C.sub.1-6 alkoxy, S(O).sub.nR.sup.21k wherein R.sup.21k is OH, C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.2-6 alkynyl, C.sub.3-10 cycloalkyl, C.sub.6-10 aryl, C.sub.6-10 aryl-C.sub.1-6 alkyl, 5- to 10-membered heteroaryl or 4- to 10-membered nonaromatic heterocyclic group, and n is 0, 1 or 2, SO.sub.2NR.sup.21mR.sup.21n wherein R.sup.21m and R.sup.21n are each independently a hydrogen atom, C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.2-6 alkynyl, C.sub.3-10 cycloalkyl, C.sub.6-10 aryl, C.sub.6-10 aryl-C.sub.1-6 alkyl, 5- to 10-membered heteroaryl or 4- to 10-membered nonaromatic heterocyclic group, and C.sub.1-3 alkylenedioxy (e.g., methylenedioxy).

(32) The anti-narcolepsy agent in the present specification means an agent for the treatment or prophylaxis of narcolepsy.

(33) The agent for improving sleepiness in the present specification means a medicament for improving daytime sleepiness due to shift work, jet lag, insomnia, sleep apnea syndrome and the like.

(34) The definition of each symbol in the formulas and preferable embodiments of the present invention are explained in the following.

(35) R.sup.1 is a hydrogen atom, C.sub.1-6 alkoxy, OH, C.sub.1-6 alkyl or a halogen atom.

(36) Examples of R.sup.1 include a hydrogen atom, methoxy, ethoxy, propoxy, OH, methyl, chlorine atom and the like.

(37) R.sup.1 is preferably C.sub.1-6 alkoxy (e.g., methoxy, ethoxy, propoxy), particularly preferably methoxy.

(38) W is (1) a group represented by the formula (iii):

(39) ##STR00010## or (2) C(O)NR.sup.WaR.sup.Wb.

(40) W is preferably a group represented by the formula (iii):

(41) ##STR00011##
wherein R.sup.15 is C.sub.1-6 alkyl (e.g., methyl) and R.sup.16 is alkyl (e.g., methyl).

(42) In another embodiment, W is preferably C(O)NR.sup.WaR.sup.Wb wherein R.sup.Wa is C.sub.1-6 alkyl (e.g., methyl, ethyl, propyl, 2,2-dimethylpropyl) (wherein C.sub.1-6 alkyl is optionally substituted by phenyl, pyridyl, C.sub.1-6 alkoxy-carbonylamino (e.g., tert-butoxycarbonylamino) or di(C.sub.1-6 alkyl)amino (e.g., dimethylamino)) or phenyl (wherein phenyl is optionally substituted by di(C.sub.1-6 alkyl)amino (e.g., dimethylamino)), and R.sup.Wb is a hydrogen atom or C.sub.1-6 alkyl (e.g., ethyl)).

(43) X is C(R.sup.5) or N, and R.sup.5 is a hydrogen atom or C.sub.1-6 alkoxy.

(44) Examples of R.sup.5 include a hydrogen atom and methoxy.

(45) R.sup.5 is preferably a hydrogen atom.

(46) X is preferably C(R.sup.5), particularly preferably CH.

(47) Any one of R.sup.2, R.sup.3 and R.sup.4 is R.sup.6 and the remaining two are each a hydrogen atom.

(48) As combinations of R.sup.2, R.sup.3 and R.sup.4, the following combinations can be mentioned. (1) R.sup.2 is R.sup.6, and R.sup.3 and R.sup.4 are each a hydrogen atom. (2) R.sup.3 is R.sup.6, and R.sup.2 and R.sup.4 are each a hydrogen atom. (3) R.sup.4 is R.sup.6, and R.sup.2 and R.sup.3 are each a hydrogen atom.

(49) Of these, the combination wherein R.sup.2 is R.sup.6, and R.sup.3 and R.sup.4 are each a hydrogen atom is preferable.

(50) R.sup.6 is (1) NR.sup.17Y.sup.1R.sup.7, (2) NHY.sup.2R.sup.10, (3) a group represented by the formula (ii):

(51) ##STR00012## (4) NNR.sup.12, or (5) NR.sup.13R.sup.14.

(52) R.sup.6 is preferably (1) NHY.sup.1R.sup.7, (2) NHY.sup.2R.sup.10, (3) a group represented by the formula (ii), or (4) NNR.sup.12, particularly preferably NHY.sup.1R.sup.7.

(53) When R.sup.6 is NR.sup.17Y.sup.1R.sup.7, Y.sup.1 is C(O)NR.sup.18, C(S)NH, C(NH)NH, C(O)O, C(O), SO.sub.2 or SO.sub.2NR.sup.8, preferably, C(O)NH, C(S)NH, C(NH)NH or C(O)O, particularly preferably C(O)NH.

(54) R.sup.8 is a hydrogen atom or C.sub.1-6 alkyl (e.g., methyl).

(55) R.sup.17 is a hydrogen atom or C.sub.1-6 alkyl (e.g., methyl), R.sup.18 is a hydrogen atom or C.sub.1-6 alkyl (e.g., methyl), or R.sup.17 and R.sup.18 are optionally bonded to each other to form, together with the nitrogen atoms bonded thereto and adjacent C(O), a 5- to 7-membered heterocycle (e.g., imidazolidin-2-one, hexahydropyrimidin-2-one, 1,3-diazepan-2-one).

(56) R.sup.17 and R.sup.18 are each preferably a hydrogen atom.

(57) R.sup.7 is (a) C.sub.6-10 aryl (e.g., phenyl, 1-naphthyl, 2-naphthyl), (b) 5- to 10-membered heteroaryl (e.g., pyridyl, thienyl, thiazolyl), (c) C.sub.1-6 alkyl (e.g., methyl, tert-butyl), or (d) C.sub.2-6 alkenyl (e.g., vinyl) wherein C.sub.1-6 alkyl and C.sub.2-6 alkenyl are optionally substituted by one substituent selected from phenyl, furyl and diphenylmethylsulfinyl, C.sub.6-10 aryl and 5- to 10-membered heteroaryl are optionally substituted by optionally selected R.sup.9 in the number of 1 to 4 (preferably 1 to 3, more preferably 1 or 2), R.sup.9 are each independently a halogen atom (e.g., bromine atom), NO.sub.2, OH, C.sub.1-6 alkyl (e.g., methyl), C.sub.1-6 haloalkyl (e.g., trifluoromethyl), C.sub.1-6 alkoxy (e.g., methoxy), 5- to 10-membered heteroaryl (e.g., pyridyl), NR.sup.9aR.sup.9b wherein R.sup.9a is a hydrogen atom, C.sub.1-6 alkyl (e.g., methyl) or C.sub.1-6 alkoxy-carbonyl (e.g., tert-butoxycarbonyl), and R.sup.9b is a hydrogen atom or C.sub.1-6 alkyl (e.g., methyl), C(O)OR.sup.9c wherein R.sup.9c is a hydrogen atom or C.sub.1-6 alkyl (e.g., methyl), C(O)NR.sup.9dR.sup.9e wherein R.sup.9d is a hydrogen atom or C.sub.1-6 alkyl (e.g., methyl), and R.sup.9e is a hydrogen atom or C.sub.1-6 alkyl (e.g., methyl), or NHC(NR.sup.9f)NHR.sup.9g wherein R.sup.9f is a hydrogen atom or C.sub.1-6 alkoxy-carbonyl (e.g., tert-butoxycarbonyl), and R.sup.9g is a hydrogen atom or C.sub.1-6 alkoxy-carbonyl (e.g., tert-butoxycarbonyl), or R.sup.9 in the number of 2 are joined to form methylenedioxy.

(58) R.sup.7 is preferably (a) C.sub.6-10 aryl (e.g., phenyl, 1-naphthyl, 2-naphthyl), or (b) 5- to 10-membered heteroaryl (e.g., pyridyl, thienyl, thiazolyl) wherein C.sub.6-10 aryl and 5- to 10-membered heteroaryl are optionally substituted by optionally selected R.sup.9 in the number of 1 to 4 (preferably 1 to 3, more preferably 1 or 2), and R.sup.9 is as defined above.

(59) R.sup.7 is particularly preferably phenyl substituted by NR.sup.9aR.sup.9b wherein R.sup.9a is C.sub.1-6 alkyl (e.g., methyl) and R.sup.9b is a hydrogen atom or C.sub.1-6 alkyl (e.g., methyl).

(60) When R.sup.6 is NHY.sup.2R.sup.10, Y.sup.2 is CH.sub.2 or a single bond.

(61) R.sup.10 is (a) C.sub.6-10 aryl (e.g., phenyl), or (b) 5- to 10-membered heteroaryl (e.g., pyridyl, thienyl, thiazolyl) wherein C.sub.6-10 aryl and 5- to 10-membered heteroaryl are optionally substituted by optionally selected R.sup.9 in the number of 1 to 4, and R.sup.9 is as defined above.

(62) R.sup.10 is preferably C.sub.6-10 aryl (e.g., phenyl) wherein C.sub.6-10 aryl is optionally substituted by optionally selected R.sup.9 in the number of 1 to 4 (preferably 1 to 3, more preferably 1 or 2), R.sup.9 are each independently a halogen atom (e.g., bromine atom), OH, C.sub.1-6 alkyl (e.g., methyl), C.sub.1-6 haloalkyl (e.g., trifluoromethyl), C.sub.1-6 alkoxy (e.g., methoxy), or C(O)NR.sup.9dR.sup.9e wherein R.sup.9d is a hydrogen atom or C.sub.1-6 alkyl (e.g., methyl), and R.sup.9e is a hydrogen atom or C.sub.1-6 alkyl (e.g., methyl), or R.sup.9 in the number of 2 are joined to form methylenedioxy.

(63) When R.sup.6 is a group represented by the formula (ii), R.sup.11 is C.sub.1-6 alkoxy (e.g., methoxy) or C.sub.6-10 arylamino (e.g., phenylamino) (wherein the C.sub.6-10 aryl moiety of C.sub.6-10 arylamino is optionally substituted by 1 to 3 substituents selected from C.sub.1-6 alkyl (e.g., methyl) and C.sub.1-6 alkoxy (e.g., methoxy).

(64) When R.sup.6 is NNR.sup.12, R.sup.12 is C.sub.6-10 aryl (e.g., phenyl) optionally substituted by 1 to 3 substituents selected from (a) C.sub.1-6 alkyl (e.g., methyl) optionally substituted by OH, (b) OH, (c) di(C.sub.1-6 alkyl)amino (e.g., dimethylamino) and (d) C.sub.1-6 alkoxy-carbonylamino (e.g., tert-butoxycarbonylamino).

(65) When R.sup.6 is NR.sup.13R.sup.14, R.sup.13 is a hydrogen atom, C.sub.1-6 alkyl (e.g., methyl), C.sub.6-10 aryl-C.sub.1-6 alkyl (e.g., benzyl) or C.sub.2-6 alkenyl-carbonyl (e.g., acryloyl), and R.sup.14 is a hydrogen atom or C.sub.1-6 alkyl (e.g., methyl, ethyl) wherein C.sub.1-6 alkyl is optionally substituted by one substituent selected from (a) C.sub.1-6 alkoxy-carbonylamino (e.g., tert-butoxycarbonylamino), (b) C.sub.2-6 alkenyl-carbonylamino (e.g., acryloylamino) and (c) C.sub.6-10 aryl-C.sub.1-6 alkylaminocarbonyl (e.g., benzylaminocarbonyl) optionally substituted by C.sub.1-6 alkyl (e.g., methyl), or R.sup.13 and R.sup.14 are bonded to each other to form, together with the nitrogen atom bonded thereto, a 5- to 7-membered heterocycle further containing one nitrogen atom (e.g., imidazolidine) wherein 5- to 7-membered heterocycle is optionally substituted by C.sub.6-10 aryl-carbonyl (e.g., benzoyl) optionally substituted by C.sub.1-6 alkyl (e.g., methyl). When R.sup.14 is ethyl substituted by C.sub.2-6 alkenyl-carbonylamino, R.sup.13 is not a hydrogen atom.

(66) R.sup.14 is preferably a hydrogen atom or C.sub.1-6 alkyl (e.g., methyl, ethyl) wherein C.sub.1-6 alkyl is optionally substituted by one substituent selected from (a) C.sub.1-6 alkoxy-carbonylamino (e.g., tert-butoxycarbonylamino) and (b) C.sub.6-10 aryl-C.sub.1-6 alkylaminocarbonyl (e.g., benzylaminocarbonyl) optionally substituted by C.sub.1-6 alkyl (e.g., methyl).

(67) As a preferable example of the compound represented by the above-mentioned formula (I) of the present invention, the following compounds can be mentioned.

(68) A compound represented by the formula (I-A):

(69) ##STR00013##
wherein each symbol is as defined in the aforementioned [1], or a pharmaceutically acceptable acid addition salt thereof.

(70) A compound represented by the formula (I-B):

(71) ##STR00014##
wherein R.sup.7a is phenyl substituted by NR.sup.9aR.sup.9b (wherein R.sup.9a is C.sub.1-6 alkyl and R.sup.9b is C.sub.1-6 alkyl), and each of other symbols is as defined in the aforementioned [1], or a pharmaceutically acceptable acid addition salt thereof.

(72) A compound represented by any of the following formulas (I-C) to (I-L) or a pharmaceutically acceptable acid addition salt thereof.

(73) ##STR00015## ##STR00016##
wherein each symbol is as defined in the aforementioned [1].

(74) In the formula (I-D), Y.sup.1 is preferably C(O)NH, C(S)NH, C(NH)NH or C(O)O, particularly preferably C(O)NH.

(75) In the formulas (I-D), (I-J), (I-K) and (I-L), R.sup.7 is preferably (a) C.sub.6-10 aryl (e.g., phenyl, 1-naphthyl, 2-naphthyl), or (b) 5- to 10-membered heteroaryl (e.g., pyridyl, thienyl, thiazolyl) wherein C.sub.6-10 aryl and 5- to 10-membered heteroaryl are optionally substituted by optionally selected R.sup.9 in the number of 1 to 4, and R.sup.9 is as defined above.

(76) R.sup.7 is particularly preferably phenyl substituted by NR.sup.9aR.sup.9b wherein R.sup.9a is C.sub.1-6 alkyl and R.sup.9b is C.sub.1-6 alkyl.

(77) [Compound I-A1]

(78) A compound of the formula (I-A) wherein R.sup.1 is a hydrogen atom, C.sub.1-6 alkoxy, OH, C.sub.1-6 alkyl or a halogen atom, X is C(R.sup.5) or N, R.sup.5 is a hydrogen atom or C.sub.1-6 alkoxy, any one of R.sup.2, R.sup.3 and R.sup.4 is R.sup.6 and the remaining two are each a hydrogen atom, R.sup.6 is (1) NR.sup.17Y.sup.1R.sup.7 wherein Y.sup.1 is C(O)NR.sup.18, C(S)NH, C(NH)NH, C(O)O, C(O), SO.sub.2 or SO.sub.2NR.sup.8, R.sup.8 is a hydrogen atom or C.sub.1-6 alkyl, R.sup.17 is a hydrogen atom or C.sub.1-6 alkyl, R.sup.18 is a hydrogen atom or C.sub.1-6 alkyl, or R.sup.17 and R.sup.18 are optionally bonded to each other to form, together with the nitrogen atoms bonded thereto and adjacent C(O), a 5- to 7-membered heterocycle (e.g., imidazolidin-2-one, hexahydropyrimidin-2-one or 1,3-diazepan-2-one), R.sup.7 is (a) C.sub.6-10 aryl (e.g., phenyl, 1-naphthyl, 2-naphthyl), (b) 5- to 10-membered heteroaryl (e.g., pyridyl, thienyl, thiazolyl), (c) C.sub.1-6 alkyl, or (d) C.sub.2-6 alkenyl (wherein C.sub.1-6 alkyl and C.sub.2-6 alkenyl are optionally substituted by one substituent selected from phenyl, furyl and diphenylmethylsulfinyl, C.sub.6-10 aryl and 5- to 10-membered heteroaryl are optionally substituted by optionally selected R.sup.9 in the number of 1 to 4 (preferably 1 to 3, more preferably 1 or 2), R.sup.9 are each independently a halogen atom, NO.sub.2, OH, C.sub.1-6 alkyl, C.sub.1-6 haloalkyl, C.sub.1-6 alkoxy, 5- to 10-membered heteroaryl (e.g., pyridyl), NR.sup.9aR.sup.9b wherein R.sup.9a is a hydrogen atom, C.sub.1-6 alkyl or C.sub.1-6 alkoxy-carbonyl, and R.sup.9b is a hydrogen atom or C.sub.1-6 alkyl, C(O)OR.sup.9c wherein R.sup.9c is a hydrogen atom or C.sub.1-6 alkyl, C(O)NR.sup.9dR.sup.9e wherein R.sup.9d is a hydrogen atom or C.sub.1-6 alkyl, and R.sup.9e is a hydrogen atom or C.sub.1-6 alkyl, or NHC(NR.sup.9f)NHR.sup.9g wherein R.sup.9f is a hydrogen atom or C.sub.1-6 alkoxy-carbonyl, and R.sup.9g is a hydrogen atom or C.sub.1-6 alkoxy-carbonyl, or R.sup.9 in the number of 2 are joined to form methylenedioxy, (2) NHY.sup.2R.sup.10 wherein Y.sup.2 is CH.sub.2 or a single bond, R.sup.10 is C.sub.6-10 aryl (e.g., phenyl) wherein C.sub.6-10 aryl is optionally substituted by optionally selected R.sup.9 in the number of 1 to 4 (preferably 1 to 3, more preferably 1 or 2), R.sup.9 are each independently a halogen atom, OH, C.sub.1-6 alkyl, C.sub.1-6 haloalkyl, C.sub.1-6 alkoxy, or C(O)NR.sup.9dR.sup.9e wherein R.sup.9d is C.sub.1-6 alkyl and R.sup.9e is C.sub.1-6 alkyl, or R.sup.9 in the number of 2 are joined to form methylenedioxy, (3) the formula (ii):

(79) ##STR00017## wherein R.sup.11 is C.sub.1-6 alkoxy or C.sub.6-10 arylamino (e.g., phenylamino) (wherein C.sub.6-10 aryl moiety of the C.sub.6-10 arylamino is optionally substituted by 1 to 3 substituents selected from C.sub.1-6 alkyl and C.sub.1-6 alkoxy), (4) NNR.sup.12 wherein R.sup.12 is C.sub.6-10 aryl (e.g., phenyl) optionally substituted by 1 to 3 substituents selected from (a) C.sub.1-6 alkyl optionally substituted by OH, (b) OH, (c) di(C.sub.1-6 alkyl)amino and (d) C.sub.1-6 alkoxy-carbonylamino, or (5) NR.sup.13R.sup.14 wherein R.sup.13 is a hydrogen atom, C.sub.1-6 alkyl, C.sub.6-10 aryl-C.sub.1-6 alkyl (e.g., benzyl) or C.sub.2-6 alkenyl-carbonyl, and R.sup.14 is a hydrogen atom or C.sub.1-6 alkyl (wherein C.sub.1-6 alkyl is optionally substituted by 1 to 3 substituents selected from (a) C.sub.1-6 alkoxy-carbonylamino, (b) C.sub.2-6 alkenyl-carbonylamino and (c) C.sub.6-10 aryl-C.sub.1-6 alkylaminocarbonyl (e.g., benzylaminocarbonyl) optionally substituted by C.sub.1-6 alkyl), or R.sup.13 and R.sup.14 are bonded to each other to form, together with the nitrogen atom bonded thereto, a 5- to 7-membered heterocycle further containing one nitrogen atom (e.g., imidazolidine) (wherein 5- to 7-membered heterocycle is optionally substituted by C.sub.6-10 aryl-carbonyl (e.g., benzoyl) optionally substituted by C.sub.1-6 alkyl), provided that when R.sup.14 is ethyl substituted by C.sub.2-6 alkenyl-carbonylamino, R.sup.13 is not a hydrogen atom, R.sup.15 is C.sub.1-6 alkyl, and R.sup.16 is C.sub.1-6 alkyl, or a pharmaceutically acceptable acid addition salt thereof.

(80) Preferably, R.sup.17 and R.sup.18 are each a hydrogen atom.

(81) [Compound I-B1]

(82) A compound of the formula (I-B) wherein R.sup.1 is C.sub.1-6 alkoxy, R.sup.7a is phenyl substituted by NR.sup.9aR.sup.9b wherein R.sup.9a is C.sub.1-6 alkyl and R.sup.9b is C.sub.1-6 alkyl, R.sup.Wa is C.sub.1-6 alkyl (wherein C.sub.1-6 alkyl is optionally substituted by phenyl, pyridyl, C.sub.1-6 alkoxy-carbonylamino or di(C.sub.1-6 alkyl)amino) or phenyl (wherein phenyl is optionally substituted by di(C.sub.1-6 alkyl)amino), and R.sup.Wb is a hydrogen atom or C.sub.1-6 alkyl, or a pharmaceutically acceptable acid addition salt thereof.
[Compound I-C1]

(83) A compound of the formula (I-C) wherein R.sup.1 is a hydrogen atom, C.sub.1-6 alkoxy, OH, C.sub.1-6 alkyl or a halogen atom, R.sup.5 is a hydrogen atom or C.sub.1-6 alkoxy, R.sup.6 is (1) NR.sup.17Y.sup.1R.sup.7 wherein Y.sup.1 is C(O)NR.sup.18, C(S)NH, C(NH)NH, C(O)O, C(O), SO.sub.2 or SO.sub.2NR.sup.8, R.sup.8 is a hydrogen atom or C.sub.1-6 alkyl, R.sup.17 is a hydrogen atom or C.sub.1-6 alkyl, R.sup.18 is a hydrogen atom or C.sub.1-6 alkyl, or R.sup.17 and R.sup.18 are optionally bonded to each other to form, together with the nitrogen atoms bonded thereto and adjacent C(O), a 5- to 7-membered heterocycle (e.g., imidazolidin-2-one, hexahydropyrimidin-2-one or 1,3-diazepan-2-one), R.sup.7 is (a) C.sub.6-10 aryl (e.g., phenyl, 1-naphthyl, 2-naphthyl), (b) 5- to 10-membered heteroaryl (e.g., pyridyl, thienyl, thiazolyl), (c) C.sub.1-6 alkyl, or (d) C.sub.2-6 alkenyl wherein C.sub.1-6 alkyl and C.sub.2-6 alkenyl are optionally substituted by one substituent selected from phenyl, furyl and diphenylmethylsulfinyl, C.sub.6-10 aryl and 5- to 10-membered heteroaryl are optionally substituted by optionally selected R.sup.9 in the number of 1 to 4 (preferably 1 to 3, more preferably 1 or 2), R.sup.9 are each independently a halogen atom, NO.sub.2, OH, C.sub.1-6 alkyl, C.sub.1-6 haloalkyl, C.sub.1-6 alkoxy, 5- to 10-membered heteroaryl (e.g., pyridyl), NR.sup.9aR.sup.9b wherein R.sup.9a is a hydrogen atom, C.sub.1-6 alkyl or C.sub.1-6 alkoxy-carbonyl and R.sup.9b is a hydrogen atom or C.sub.1-6 alkyl, C(O)OR.sup.9c wherein R.sup.9c is a hydrogen atom or C.sub.1-6 alkyl, C(O)NR.sup.9dR.sup.9e wherein R.sup.9d is a hydrogen atom or C.sub.1-6 alkyl and R.sup.9e is a hydrogen atom or C.sub.1-6 alkyl, or NHC(NR.sup.9f)NHR.sup.9g wherein R.sup.9f is a hydrogen atom or C.sub.1-6 alkoxy-carbonyl and R.sup.9g is a hydrogen atom or C.sub.1-6 alkoxy-carbonyl, or R.sup.9 in the number of 2 are joined to form methylenedioxy, (2) NHY.sup.2R.sup.10 wherein Y.sup.2 is CH.sub.2 or a single bond, R.sup.10 is C.sub.6-10 aryl (e.g., phenyl) wherein C.sub.6-10 aryl is optionally substituted by optionally selected R.sup.9 in the number of 1 to 4 (preferably 1 to 3, more preferably 1 or 2), R.sup.9 are each independently a halogen atom, OH, C.sub.1-6 alkyl, C.sub.1-6 haloalkyl, C.sub.1-6 alkoxy, or C(O)NR.sup.9dR.sup.9e wherein R.sup.9d is C.sub.1-6 alkyl and R.sup.9e is C.sub.1-6 alkyl, or R.sup.9 in the number of 2 are joined to form methylenedioxy, (3) a group represented by the formula (ii):

(84) ##STR00018## wherein R.sup.11 is C.sub.1-6 alkoxy or C.sub.6-10 arylamino (e.g., phenylamino) wherein the C.sub.6-10 aryl moiety of C.sub.6-10 arylamino is optionally substituted by 1 to 3 substituents selected from C.sub.1-6 alkyl and C.sub.1-6 alkoxy, (4) NNR.sup.12 wherein R.sup.12 is C.sub.6-10 aryl (e.g., phenyl) optionally substituted 1 to 3 substituents selected from (a) C.sub.1-6 alkyl optionally substituted by OH, (b) OH, (c) di(C.sub.1-6 alkyl)amino and (d) C.sub.1-6 alkoxy-carbonylamino, or (5) NR.sup.13R.sup.14 wherein R.sup.13 is a hydrogen atom, C.sub.1-6 alkyl, C.sub.6-10 aryl-C.sub.1-6 alkyl (e.g., benzyl) or C.sub.2-6 alkenyl-carbonyl, and R.sup.14 is a hydrogen atom or C.sub.1-6 alkyl wherein C.sub.1-6 alkyl is optionally substituted by one substituent selected from (a) C.sub.1-6 alkoxy-carbonylamino, (b) C.sub.2-6 alkenyl-carbonylamino and (c) C.sub.6-10 aryl-C.sub.1-6 alkylaminocarbonyl (e.g., benzylaminocarbonyl) optionally substituted by C.sub.1-6 alkyl, or R.sup.13 and R.sup.14 are bonded to each other to form, together with the nitrogen atom bonded thereto, a 5- to 7-membered heterocycle further containing one nitrogen atom (e.g., imidazolidine) (wherein 5- to 7-membered heterocycle is optionally substituted by C.sub.6-10 aryl-carbonyl (e.g., benzoyl) optionally substituted by C.sub.1-6 alkyl), provided that when R.sup.14 is ethyl substituted by C.sub.2-6 alkenyl-carbonylamino, R.sup.13 is not a hydrogen atom, R.sup.15 is C.sub.1-6 alkyl, and R.sup.16 is C.sub.1-6 alkyl, or a pharmaceutically acceptable acid addition salt thereof.
[Compound I-D1]

(85) A compound of the formula (I-D) wherein R.sup.1 is a hydrogen atom, C.sub.1-6 alkoxy, OH, C.sub.1-6 alkyl or a halogen atom, R.sup.5 is a hydrogen atom or C.sub.1-6 alkoxy, Y.sup.1 is C(O)NR.sup.18, C(S)NH, C(NH)NH, C(O)O, C(O), SO.sub.2 or SO.sub.2NR.sup.8, R.sup.8 is a hydrogen atom or C.sub.1-6 alkyl, R.sup.18 is a hydrogen atom, R.sup.7 is (a) C.sub.6-10 aryl (e.g., phenyl, 1-naphthyl, 2-naphthyl), (b) 5- to 10-membered heteroaryl (e.g., pyridyl, thienyl, thiazolyl), (c) C.sub.1-6 alkyl, or (d) C.sub.2-6 alkenyl wherein C.sub.1-6 alkyl and C.sub.2-6 alkenyl are optionally substituted by one substituent selected from phenyl, furyl and diphenylmethylsulfinyl, C.sub.6-10 aryl and 5- to 10-membered heteroaryl are optionally substituted by optionally selected R.sup.9 in the number of 1 to 4 (preferably 1 to 3, more preferably 1 or 2), R.sup.9 are each independently a halogen atom, NO.sub.2, OH, C.sub.1-6 alkyl, C.sub.1-6 haloalkyl, C.sub.1-6 alkoxy, 5- to 10-membered heteroaryl (e.g., pyridyl), NR.sup.9aR.sup.9b wherein R.sup.9a is a hydrogen atom, C.sub.1-6 alkyl or C.sub.1-6 alkoxy-carbonyl and R.sup.9b is a hydrogen atom or C.sub.1-6 alkyl, C(O)OR.sup.9c wherein R.sup.9c is a hydrogen atom or C.sub.1-6 alkyl, C(O)NR.sup.9dR.sup.9e wherein R.sup.9d is a hydrogen atom or C.sub.1-6 alkyl and R.sup.9e is a hydrogen atom or C.sub.1-6 alkyl, or NHC(NR.sup.9f)NHR.sup.9g wherein R.sup.9f is a hydrogen atom or C.sub.1-6 alkoxy-carbonyl and R.sup.9g is a hydrogen atom or C.sub.1-6 alkoxy-carbonyl, or R.sup.9 in the number of 2 are joined to form methylenedioxy, R.sup.15 is C.sub.1-6 alkyl, and R.sup.16 is C.sub.1-6 alkyl, or a pharmaceutically acceptable acid addition salt thereof.
[Compound I-D2]

(86) A compound of the formula (I-D) wherein R.sup.1 is a hydrogen atom, C.sub.1-6 alkoxy, OH, C.sub.1-6 alkyl or a halogen atom, R.sup.5 is a hydrogen atom or C.sub.1-6 alkoxy, Y.sup.1 is C(O)NR.sup.18, C(S)NH or C(NH)NH, R.sup.8 is a hydrogen atom or C.sub.1-6 alkyl, R.sup.18 is a hydrogen atom, R.sup.7 is (a) C.sub.6-10 aryl (e.g., phenyl), or (b) 5- to 10-membered heteroaryl (e.g., pyridyl, thienyl) wherein C.sub.6-10 aryl and 5- to 10-membered heteroaryl are optionally substituted by optionally selected R.sup.9 in the number of 1 to 4 (preferably 1 to 3, more preferably 1 or 2), R.sup.9 are each independently a halogen atom, NO.sub.2, OH, C.sub.1-6 alkyl, C.sub.1-6 haloalkyl, C.sub.1-6 alkoxy, 5- to 10-membered heteroaryl (e.g., pyridyl), NR.sup.9aR.sup.9b wherein R.sup.9a is a hydrogen atom, C.sub.1-6 alkyl or C.sub.1-6 alkoxy-carbonyl and R.sup.9b is a hydrogen atom or C.sub.1-6 alkyl, C(O)OR.sup.9c wherein R.sup.9c is a hydrogen atom or C.sub.1-6 alkyl, C(O)NR.sup.9dR.sup.9e wherein R.sup.9d is a hydrogen atom or C.sub.1-6 alkyl and R.sup.9e is a hydrogen atom or C.sub.1-6 alkyl, or NHC(NR.sup.9f)NHR.sup.9g wherein R.sup.9f is a hydrogen atom or C.sub.1-6 alkoxy-carbonyl and R.sup.9g is a hydrogen atom or C.sub.1-6 alkoxy-carbonyl, or R.sup.9 in the number of 2 are joined to form methylenedioxy, R.sup.15 is C.sub.1-6 alkyl, and R.sup.16 is C.sub.1-6 alkyl, or a pharmaceutically acceptable acid addition salt thereof.
[Compound I-E1]

(87) A compound of the formula (I-E) wherein R.sup.1 is C.sub.1-6 alkoxy, R.sup.5 is a hydrogen atom, Y.sup.2 is CH.sub.2 or a single bond, R.sup.10 is C.sub.6-10 aryl (e.g., phenyl) wherein C.sub.6-10 aryl is optionally substituted by optionally selected R.sup.9 in the number of 1 to 4 (preferably 1 to 3, more preferably 1 or 2), R.sup.9 are each independently a halogen atom, OH, C.sub.1-6 alkyl, C.sub.1-6 haloalkyl, C.sub.1-6 alkoxy, or C(O)NR.sup.9dR.sup.9e wherein R.sup.9d is C.sub.1-6 alkyl and R.sup.9e is C.sub.1-6 alkyl, or R.sup.9 in the number of 2 are joined to form methylenedioxy, R.sup.15 is C.sub.1-6 alkyl and R.sup.16 is C.sub.1-6 alkyl, or a pharmaceutically acceptable acid addition salt thereof.
[Compound I-F1]

(88) A compound of the formula (I-F) wherein R.sup.1 is C.sub.1-6 alkoxy, R.sup.5 is a hydrogen atom, R.sup.11 is C.sub.1-6 alkoxy or C.sub.6-10 arylamino (e.g., phenylamino) wherein the C.sub.6-10 aryl moiety of C.sub.6-10 arylamino is optionally substituted by one substituent selected from C.sub.1-6 alkyl and C.sub.1-6 alkoxy, R.sup.15 is C.sub.1-6 alkyl and R.sup.16 is C.sub.1-6 alkyl, or a pharmaceutically acceptable acid addition salt thereof.
[Compound I-G1]

(89) A compound of the formula (I-G) wherein R.sup.1 is C.sub.1-6 alkoxy, R.sup.5 is a hydrogen atom, R.sup.12 is C.sub.6-10 aryl (e.g., phenyl) optionally substituted by 1 or 2 substituents selected from (a) C.sub.1-6 alkyl optionally substituted by OH, (b) OH, (c) di(C.sub.1-6 alkyl)amino and (d) C.sub.1-6 alkoxy-carbonylamino, R.sup.15 is C.sub.1-6 alkyl, and R.sup.16 is C.sub.1-6 alkyl, or a pharmaceutically acceptable acid addition salt thereof.
[Compound I-H1]

(90) A compound of the formula (I-H) wherein R.sup.1 is C.sub.1-6 alkoxy, R.sup.5 is a hydrogen atom, R.sup.13 is a hydrogen atom, C.sub.1-6 alkyl, C.sub.6-10 aryl-C.sub.1-6 alkyl (e.g., benzyl) or C.sub.2-6 alkenyl-carbonyl and R.sup.14 is a hydrogen atom or C.sub.1-6 alkyl wherein C.sub.1-6 alkyl is optionally substituted by one substituent selected from (a) C.sub.1-6 alkoxy-carbonylamino, (b) C.sub.2-6 alkenyl-carbonylamino and (c) C.sub.6-10 aryl-C.sub.1-6 alkylaminocarbonyl (e.g., benzylaminocarbonyl) optionally substituted by C.sub.1-6 alkyl, or R.sup.13 and R.sup.14 are bonded to each other to form, together with the nitrogen atom bonded thereto, a 5- to 7-membered heterocycle further containing one nitrogen atom (e.g., imidazolidine) wherein 5- to 7-membered heterocycle is optionally substituted by C.sub.6-10 aryl-carbonyl (e.g., benzoyl) optionally substituted by C.sub.1-6 alkyl, provided that when R.sup.14 is ethyl substituted by C.sub.2-6 alkenyl-carbonylamino, R.sup.13 is not a hydrogen atom, R.sup.15 is C.sub.1-6 alkyl, and R.sup.16 is C.sub.1-6 alkyl, or a pharmaceutically acceptable acid addition salt thereof.
[Compound I-J1]

(91) A compound of the formula (I-J) wherein R.sup.1 is C.sub.1-6 alkoxy, R.sup.7 is phenyl substituted by NR.sup.9aR.sup.9b wherein R.sup.9a is C.sub.1-6 alkyl and R.sup.9b is C.sub.1-6 alkyl, R.sup.15 is C.sub.1-6 alkyl, and R.sup.16 is C.sub.1-6 alkyl, or a pharmaceutically acceptable acid addition salt thereof.
[Compound I-K1]

(92) A compound of the formula (I-K) wherein R.sup.1 is C.sub.1-6 alkoxy, R.sup.7 is phenyl substituted by NR.sup.9aR.sup.9b wherein R.sup.9a is C.sub.1-6 alkyl and R.sup.9b is C.sub.1-6 alkyl, R.sup.15 is C.sub.1-6 alkyl, and R.sup.16 is C.sub.1-6 alkyl, or a pharmaceutically acceptable acid addition salt thereof.
[Compound I-L1]

(93) A compound of the formula (I-L) wherein R.sup.1 is C.sub.1-6 alkoxy, R.sup.7 is phenyl substituted by NR.sup.9aR.sup.9b wherein R.sup.9a is C.sub.1-6 alkyl and R.sup.9b is C.sub.1-6 alkyl, R.sup.15 is C.sub.1-6 alkyl, and R.sup.16 is C.sub.1-6 alkyl, or a pharmaceutically acceptable acid addition salt thereof.

(94) As a pharmaceutically acceptable acid addition salt of the compound of the formula (I) or (I) of the present invention, inorganic acid salts such as hydrochloride, sulfate, nitrate, hydrobromide, hydroiodide, phosphate and the like, organic carbonates such as acetate, lactate, citrate, oxalate, glutarate, malate, tartrate, fumarate, mandelate, maleate, benzoate, phthalate and the like, organic sulfonates such as methanesulfonate, ethanesulfonate, benzenesulfonate, p-toluenesulfonate, camphorsulfonate and the like, and the like can be mentioned; however, these are not limitative. Of these, hydrochloride, hydrobromide, phosphate, tartrate, methanesulfonate or camphorsulfonate is preferable, and hydrochloride, tartrate or methanesulfonate is further preferably used and hydrochloride is particularly preferably used; however, these are also not limitative.

(95) The compound of the above-mentioned formula (I) or (I) of the present invention can be produced by an appropriate method based on the characteristics derived from the basic skeleton and substituents thereof. While the starting materials and reagents to be used for the production of these compounds are generally available or can be synthesized by a method known to those of ordinary skill in the art, which follows the procedures described in reference documents such as Organic Reactions (Wiley & Sons), Fieser and Fieser's Reagent for Organic Synthesis (Wiley & Sons) and the like.

(96) As a specific production method of the compound of the above-mentioned formula (I) or (I) of the present invention, for example, the methods shown in Schemes 1 to 18 can be mentioned.

(97) ##STR00019##
wherein R.sup.1, R.sup.7, X and W are as defined above, X.sup.1 is a halogen atom such as chlorine atom, bromine atom and the like or a hydroxy group, and Boc is a tert-butoxycarbonyl group.
Step 1

(98) Compound (IV) can be obtained by, for example, amidating sulfonyl chloride compound (II) with amine compound (III).

(99) As the solvent, halogenated hydrocarbon solvents such as dichloromethane, chloroform, 1,2-dichloroethane and the like, ether solvents such as diethyl ether, tetrahydrofuran (THF), 1,2-dimethoxyethane (DME), dioxane and the like, aprotic polar solvents such as N,N-dimethylformamide (DMF), dimethyl sulfoxide (DMSO) and the like or a mixed solvent thereof can be used. Generally, dichloromethane or THF is preferably used. The sulfonyl chloride compound (II) is used in an amount of 0.5-20 equivalents, preferably 1.0-10 equivalents, relative to amine compound (III).

(100) Examples of the base include sodium carbonate, potassium carbonate, cesium carbonate, potassium phosphate, sodium hydroxide, potassium hydroxide, barium hydroxide, triethylamine, diisopropylethylamine, pyridine, 4-dimethylaminopyridine and the like, and diisopropylethylamine, triethylamine or pyridine is preferably used.

(101) The reaction temperature is generally 40-150 C., preferably 0-80 C. While the reaction time is appropriately selected according to the conditions such as reaction temperature and the like, it is generally about 10 min-48 hr. While the concentration of substrate (II) in the reaction system is not particularly limited, it is generally preferably 0.001 mmol/L-1 mol/L.

(102) Step 2

(103) Amine compound (V) can be obtained by, for example, deprotection of a tert-butoxycarbonyl (Boc) group of compound (IV) under acidic conditions.

(104) As the solvent, halogenated hydrocarbon solvents such as dichloromethane, chloroform, 1,2-dichloroethane and the like, ether solvents such as THF, DME, dioxane and the like, alcohol solvents such as methanol, ethanol, propanol and the like or a mixed solvent thereof can be used. In general, dichloromethane or dioxane is preferably used.

(105) As the acid, organic acids such as trifluoroacetic acid, methanesulfonic acid, p-toluenesulfonic acid, trifluoromethanesulfonic acid and the like, or inorganic acids such as hydrochloric acid, hydrobromic acid, hydroiodic acid, sulfuric acid, nitric acid, phosphoric acid and the like can be used. In general, trifluoroacetic acid or hydrochloric acid is preferably used. In another method, a hydrogen chloride-methanol solution, a hydrogen chloride-THF solution, a hydrogen chloride-ethyl acetate solution, or a hydrogen chloride-dioxane solution obtained by dissolving hydrogen chloride in an organic solvent is each independently used. In this case, particularly, preferable results are obtained by using a hydrogen chloride-methanol solution or a hydrogen chloride-THF solution. The acid is used in an amount of 1.0-100 equivalents, preferably 3.0-10 equivalents, relative to compound (IV).

(106) The reaction temperature is generally 40-150 C., preferably 0-80 C. While the reaction time is appropriately selected according to the conditions such as reaction temperature and the like, it is generally about 20 min-48 hr. While the concentration of substrate (IV) in the reaction system is not particularly limited, it is generally preferably 0.001 mmol/L-1 mol/L.

(107) Step 3

(108) Compound (I-1) can be obtained by, for example, amidation of amine compound (V) with acyl halide compound (VI) wherein X.sup.1 is a halogen atom.

(109) As the solvent, halogenated hydrocarbon solvents such as dichloromethane, chloroform, 1,2-dichloroethane and the like, ether solvents such as diethyl ether, THF, DME, dioxane and the like, aprotic polar solvents such as DMF, DMSO and the like or a mixed solvent thereof can be used. In general, dichloromethane or THF is preferably used. The acyl halide compound (VI) is used in an amount of 0.5-20 equivalents, preferably 1.0-10 equivalents, relative to amine compound (V).

(110) Examples of the base include sodium carbonate, potassium carbonate, cesium carbonate, potassium phosphate, sodium hydroxide, potassium hydroxide, barium hydroxide, triethylamine, diisopropylethylamine, pyridine, 4-dimethylaminopyridine and the like, and diisopropylethylamine, triethylamine or pyridine is preferably used.

(111) The reaction temperature is generally 40-150 C., preferably 0-80 C. While the reaction time is appropriately selected according to the conditions such as reaction temperature and the like, it is generally about 10 min-48 hr. While the concentration of substrate (V) in the reaction system is not particularly limited, it is generally preferably 0.001 mmol/L-1 mol/L.

(112) In addition, compound (I-1) can be obtained by, for example, amidation of amine compound (V) with carboxylic acid (VI) wherein X.sup.1 is a hydroxy group.

(113) As the solvent, halogenated hydrocarbon solvents such as dichloromethane, chloroform, 1,2-dichloroethane and the like, ether solvents such as diethyl ether, THF, DME, dioxane and the like, aprotic polar solvents such as DMF, DMSO, ethyl acetate and the like, alcohol solvents such as methanol, ethanol, propanol and the like or a mixed solvent thereof can be used. Generally, dichloromethane or THF is preferably used. The carboxylic acid (VI) is used in an amount of 0.5-20 equivalents, preferably 0.5-10 equivalents, relative to amine compound (V).

(114) As the condensing agent, dicyclohexylcarbodiimide, 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (EDCI), benzotriazol-1-yloxytris(dimethylamino)phosphonium hexafluorophosphate (BOP), N,N-carbonyldiimidazole (CDI), 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride (DMT-MM), {{[(1-cyano-2-ethoxy-2-oxoethylidene)amino]oxy}-4-morpholinomethylene}dimethylammonium hexafluorophosphate (COMU), O-(7-azabenzotriazol-1-yl)-N,N,N,N-tetramethyluronium hexafluorophosphate (HATU) and the like can be used, and particularly, BOP or HATU is preferably used. The condensing agent is used in an amount of 1.0-100 equivalents, preferably 1.0-10 equivalents, relative to amine compound (XXI).

(115) When a base is used, triethylamine, diisopropylethylamine, pyridine, N-methylmorpholine and the like can be used, and triethylamine or diisopropylethylamine is preferably used. The base is used in an amount of 3.0-100 equivalents, preferably 3.0-10 equivalents, relative to amine compound (V).

(116) The reaction temperature is generally 40-150 C., preferably 0-60 C. While the reaction time is appropriately selected according to the conditions such as reaction temperature and the like, it is generally about 20 min-48 hr. While the concentration of substrate (V) in the reaction system is not particularly limited, it is generally preferably 0.001 mmol/L-1 mol/L.

(117) ##STR00020##
wherein R.sup.1, R.sup.10, X and W are as defined above.

(118) Compound (I-2) can be obtained by, for example, reductive alkylation of amine compound (V) with aldehyde compound (VII).

(119) As the solvent, halogenated hydrocarbon solvents such as dichloromethane, chloroform, 1,2-dichloroethane and the like, ether solvents such as diethyl ether, THF, DME, dioxane and the like, aprotic polar solvents such as DMF, DMSO and the like, alcohol solvents such as methanol, ethanol, propanol and the like, acetic acid, water or a mixed solvent thereof can be used. The aldehyde compound (VII) is used in an amount of 0.5-20 equivalents, preferably 1.0-10 equivalents, relative to amine compound (V).

(120) Examples of the reducing agent include sodium borohydride, lithium borohydride, sodium cyanoborohydride, sodium triacetoxyborohydride, 2-picoline-borane complex and the like.

(121) When a base is used, triethylamine, diisopropylethylamine, pyridine, N-methylmorpholine and the like can be used, and triethylamine or diisopropylethylamine is preferably used.

(122) The reaction temperature is generally 40-150 C., preferably 0-80 C. While the reaction time is appropriately selected according to the conditions such as reaction temperature and the like, it is generally about 10 min-48 hr. While the concentration of substrate (V) in the reaction system is not particularly limited, it is generally preferably 0.001 mmol/L-1 mol/L.

(123) ##STR00021##
wherein R.sup.1, R.sup.10, X and W is as defined above.

(124) Compound (I-3) can be obtained by, for example, subjecting amine compound (V) to a coupling reaction with boronic acid compound (VIII) in the presence of a copper catalyst.

(125) As the solvent, halogenated hydrocarbon solvents such as dichloromethane, chloroform, 1,2-dichloroethane and the like, ether solvents such as THF, DME, dioxane and the like, aprotic polar solvents such as DMF, DMSO and the like, alcohol solvents such as methanol, ethanol, propanol and the like, aromatic hydrocarbon solvents such as benzene, toluene, xylene and the like or a mixed solvent thereof can be used. The boronic acid compound (VIII) is used in an amount of 1.0-20 equivalents, preferably 1.0-10 equivalents, relative to amine compound (V).

(126) As the copper catalyst, copper acetate (II) and the like can be mentioned. The copper catalyst is used in an amount of 0.001-1 equivalents, preferably 0.005-0.5 equivalents, relative to amine compound (V).

(127) When a base is used, triethylamine, diisopropylethylamine, pyridine, N-methylmorpholine and the like can be used, and triethylamine or diisopropylethylamine is preferably used.

(128) The reaction temperature is generally 40-150 C., preferably 0-80 C. While the reaction time is appropriately selected according to the conditions such as reaction temperature and the like, it is generally about 20 min-48 hr. While the concentration of substrate (V) in the reaction system is not particularly limited, it is generally preferably 0.001 mmol/L-1 mol/L.

(129) ##STR00022##
wherein R.sup.1, R.sup.7, X and W are as defined above.

(130) Compound (I-4) can be obtained by reacting, for example, amine compound (V) with isocyanate (IX) or isocyanate (IX) developed from carboxylic acid R.sup.7CO.sub.2H (IX-1).

(131) As the solvent, halogenated hydrocarbon solvents such as dichloromethane, chloroform, 1,2-dichloroethane and the like, ether solvents such as THF, DME, dioxane and the like, aprotic polar solvents such as DMF, DMSO and the like, aromatic hydrocarbon solvents such as benzene, toluene, xylene and the like or a mixed solvent thereof can be used. Isocyanate (IX) is used in an amount of 1.0-20 equivalents, preferably 1.0-10 equivalents, relative to amine compound (V).

(132) When a base is used, triethylamine, diisopropylethylamine, pyridine, N-methylmorpholine and the like can be used, and triethylamine or diisopropylethylamine is preferably used.

(133) The reaction temperature is generally 40-150 C., preferably 0-80 C. While the reaction time is appropriately selected according to the conditions such as reaction temperature and the like, it is generally about 20 min-48 hr. While the concentration of substrate (V) in the reaction system is not particularly limited, it is generally preferably 0.001 mmol/L-1 mol/L.

(134) When isocyanate (IX) is developed from carboxylic acid (IX-1), for example, it can be obtained by converting carboxylic acid (IX-1) to an acid azide with diphenylphosphoryl azide (DPPA) and subjecting the same to Curtius rearrangement reaction under heating conditions.

(135) As the solvent, halogenated hydrocarbon solvents such as dichloromethane, chloroform, 1,2-dichloroethane and the like, ether solvents such as THF, DME, dioxane and the like, aprotic polar solvents such as DMF, DMSO and the like, aromatic hydrocarbon solvents such as benzene, toluene, xylene and the like or a mixed solvent thereof can be used. The carboxylic acid (IX-1) is used in an amount of 1.0-30 equivalents, preferably 1.0-10 equivalents, relative to amine compound (V). DPPA is used in an amount of 1.0-30 equivalents, preferably 1.0-10 equivalents, relative to carboxylic acid (IX-1).

(136) When a base is used, triethylamine, diisopropylethylamine, pyridine, N-methylmorpholine and the like can be used, and triethylamine or diisopropylethylamine is preferably used.

(137) The reaction temperature is generally 40-150 C., preferably 0-80 C. While the reaction time is appropriately selected according to the conditions such as reaction temperature and the like, it is generally about 20 min-48 hr. While the concentration of substrate (V) in the reaction system is not particularly limited, it is generally preferably 0.001 mmol/L-1 mol/L.

(138) ##STR00023##
wherein R.sup.1, R.sup.7, X and W are as defined above.

(139) Compound (I-5) can be obtained by reacting, for example, amine compound (V) with isothiocyanate (X).

(140) As the solvent, halogenated hydrocarbon solvents such as dichloromethane, chloroform, 1,2-dichloroethane and the like, ether solvents such as THF, DME, dioxane and the like, aprotic polar solvents such as DMF, DMSO and the like, aromatic hydrocarbon solvents such as benzene, toluene, xylene and the like or a mixed solvent thereof can be used. Isothiocyanate (X) is used in an amount of 1.0-20 equivalents, preferably 1.0-10 equivalents, relative to amine compound (V).

(141) When a base is used, triethylamine, diisopropylethylamine, pyridine, N-methylmorpholine and the like can be used, and triethylamine or diisopropylethylamine is preferably used.

(142) The reaction temperature is generally 40-150 C., preferably 0-80 C. While the reaction time is appropriately selected according to the conditions such as reaction temperature and the like, it is generally about 20 min-48 hr. While the concentration of substrate (V) in the reaction system is not particularly limited, it is generally preferably 0.001 mmol/L-1 mol/L.

(143) ##STR00024##
wherein R.sup.1, R.sup.7, X and W are as defined above.

(144) Compound (I-6) can be obtained by reacting, for example, compound (I-5) with ammonia and 2-iodoxybenzoic acid (IBX).

(145) As the solvent, nitrile solvents such as acetonitrile and the like can be used. As ammonia, an aqueous ammonia solution can be used. Ammonia and IBX are used in an amount of 1.0-20 equivalents, preferably 1.0-10 equivalents, relative to compound (I-6).

(146) The reaction temperature is generally 40-150 C., preferably 0-80 C. While the reaction time is appropriately selected according to the conditions such as reaction temperature and the like, it is generally about 20 min-48 hr. While the concentration of the substrate (I-6) in the reaction system is not particularly limited, it is generally preferably 0.001 mmol/L-1 mol/L.

(147) ##STR00025##
wherein R.sup.1, R.sup.7, X and W are as defined above.

(148) Compound (I-7) can be obtained by reacting, for example, amine compound (V) with chloroformic acid ester (XI).

(149) As the solvent, halogenated hydrocarbon solvents such as dichloromethane, chloroform, 1,2-dichloroethane and the like, ether solvents such as THF, DME, dioxane and the like, aprotic polar solvents such as DMF, DMSO and the like, aromatic hydrocarbon solvents such as benzene, toluene, xylene and the like or a mixed solvent thereof can be used. The chloroformic acid ester (XI) is used in an amount of 1.0-20 equivalents, preferably 1.0-10 equivalents, relative to amine compound (V).

(150) When a base is used, triethylamine, diisopropylethylamine, pyridine, N-methylmorpholine and the like can be used, and triethylamine or diisopropylethylamine is preferably used.

(151) The reaction temperature is generally 40-150 C., preferably 0-80 C. While the reaction time is appropriately selected according to the conditions such as reaction temperature and the like, it is generally about 20 min-48 hr. While the concentration of substrate (V) in the reaction system is not particularly limited, it is generally preferably 0.001 mmol/L-1 mol/L.

(152) ##STR00026##
wherein R.sup.1, X and W are as defined above, R.sup.11a is C.sub.1-6 alkoxy, and R.sup.11b is C.sub.6-10 aryl optionally substituted by 1 to 3 substituents selected from C.sub.1-6 alkyl and C.sub.1-6 alkoxy.
Step 1

(153) Compound (I-8) can be obtained by reacting, for example, amine compound (V) with cyclobutene compound (XII).

(154) As the solvent, halogenated hydrocarbon solvents such as dichloromethane, chloroform, 1,2-dichloroethane and the like, ether solvents such as THF, DME, dioxane and the like, aprotic polar solvents such as DMF, DMSO and the like, alcohol solvents such as methanol, ethanol, propanol and the like, aromatic hydrocarbon solvents such as benzene, toluene, xylene and the like or a mixed solvent thereof can be used. The cyclobutene compound (XII) is used in an amount of 1.0-20 equivalents, preferably 1.0-10 equivalents, relative to amine compound (V).

(155) When a base is used, triethylamine, diisopropylethylamine, pyridine, N-methylmorpholine and the like can be used, and triethylamine or diisopropylethylamine is preferably used.

(156) The reaction temperature is generally 40-150 C., preferably 0-80 C. While the reaction time is appropriately selected according to the conditions such as reaction temperature and the like, it is generally about 20 min-48 hr. While the concentration of substrate (V) in the reaction system is not particularly limited, it is generally preferably 0.001 mmol/L-1 mol/L.

(157) Step 2

(158) Compound (I-9) can be obtained by reacting, for example, compound (I-8) wherein R.sup.11a is methoxy with amine compound (XIII).

(159) As the solvent, halogenated hydrocarbon solvents such as dichloromethane, chloroform, 1,2-dichloroethane and the like, ether solvents such as THF, DME, dioxane and the like, aprotic polar solvents such as DMF, DMSO and the like, alcohol solvents such as methanol, ethanol, propanol and the like, aromatic hydrocarbon solvents such as benzene, toluene, xylene and the like or a mixed solvent thereof can be used. The amine compound (XIII) is used in an amount of 1.0-20 equivalents, preferably 1.0-10 equivalents, relative to compound (I-8).

(160) When a base is used, triethylamine, diisopropylethylamine, pyridine, N-methylmorpholine and the like can be used, and triethylamine or diisopropylethylamine is preferably used.

(161) The reaction temperature is generally 40-150 C., preferably 0-80 C. While the reaction time is appropriately selected according to the conditions such as reaction temperature and the like, it is generally about 20 min-48 hr. While the concentration of substrate (I-8) in the reaction system is not particularly limited, it is generally preferably 0.001 mmol/L-1 mol/L.

(162) ##STR00027##
wherein R.sup.1, R.sup.7, X and W are as defined above.

(163) Compound (I-10) can be obtained by, for example, amidation of amine compound (V) with sulfonyl chloride compound (XIV).

(164) Amidation can be performed by a method similar to Scheme 1, Step 1.

(165) ##STR00028##
wherein R.sup.1, R.sup.7, R.sup.8, X and W are as defined above.

(166) Compound (I-11) can be obtained by, for example, amidation of amine compound (V) with sulfonyl chloride compound (XV).

(167) Amidation can be performed by a method similar to Scheme 1, Step 1.

(168) ##STR00029##
wherein R.sup.1, X, W and X.sup.1 are as defined above, R.sup.20 is C.sub.6-10 aryl optionally substituted by C.sub.1-6 alkyl, and Bn is a benzyl group.
Step 1

(169) Compound (XVIII) can be obtained by, for example, amidation of sulfonyl chloride compound (XVI) with amine compound (XVII).

(170) Amidation can be performed by a method similar to Scheme 1, Step 1.

(171) Step 2

(172) Compound (XX) can be obtained by, for example, Suzuki coupling of compound (XVIII) with boronic acid compound (XIX).

(173) The Suzuki coupling reaction is performed in the presence of a palladium catalyst and a base, in the presence or absence of a phosphine ligand in a suitable solvent.

(174) As the solvent, ether solvents such as THF, DME, dioxane and the like, aprotic polar solvents such as DMF, DMSO and the like, alcohol solvents such as methanol, ethanol, propanol and the like, aromatic hydrocarbon solvents such as benzene, toluene, xylene and the like, water or a mixed solvent thereof can be used. In general, dioxane, DME, a mixed solvent of dioxane and water or a mixed solvent of DME and water is preferably used.

(175) As boronic acid compound (XIX), not only boronic acid but also boronates such as boronic acid pinacol ester, N-methyliminodiacetic acid (MIDA) boronate and the like, or potassium trifluoroborate salt can be used. Particularly, boronic acid or boronic acid pinacol ester is preferably used. The boronic acid compound (XIX) is used in an amount of 1.0-20 equivalents, preferably 1.0-10 equivalents, relative to compound (XVIII).

(176) Examples of the palladium catalyst include tetrakis(triphenylphosphine)palladium, palladium acetate, bis(triphenylphosphine)palladium dichloride, bis(dibenzylideneacetone)palladium, bis(diphenylphosphino)ferrocene palladium dichloride and the like, and tetrakis(triphenylphosphine)palladium or bis(diphenylphosphino)ferrocene palladium dichloride is preferably used. The palladium catalyst is used in an amount of 0.001-1 equivalent, preferably 0.005-0.5 equivalent, relative to compound (XVIII).

(177) Examples of the base include sodium carbonate, potassium carbonate, cesium carbonate, potassium phosphate, sodium hydroxide, potassium hydroxide, barium hydroxide, triethylamine, diisopropylethylamine and the like, and sodium carbonate or potassium carbonate is preferably used.

(178) The reaction temperature is generally 40-150 C., preferably 20-110 C. While the reaction time is appropriately selected according to the conditions such as reaction temperature and the like, it is generally about 20 min-48 hr. While the concentration of substrate (XIX) in the reaction system is not particularly limited, it is generally preferably 0.001 mmol/L-1 mol/L.

(179) Step 3

(180) Amine compound (XXI) can be obtained by, for example, deprotecting the benzyl group of compound (XX) by hydrogenolysis and the like, and deprotecting the tert-butoxycarbonyl (Boc) group of the obtained compound under acidic conditions.

(181) Hydrogenolysis is performed in the presence of a palladium catalyst and under hydrogen atmosphere in a suitable solvent.

(182) As the solvent, ether solvents such as THF, DME, dioxane and the like, aprotic polar solvents such as DMF, DMSO, ethyl acetate and the like, alcohol solvents such as methanol, ethanol, propanol and the like, aromatic hydrocarbon solvents such as benzene, toluene, xylene and the like, acetic acid, water or a mixed solvent thereof can be used. Generally, toluene, THF or methanol is preferably used.

(183) Examples of the palladium catalyst include palladium (Pd), palladium carbon (Pd/C), palladium hydroxide (Pd(OH).sub.2), palladium hydroxide carbon (Pd(OH).sub.2/C) and the like, and palladium carbon (Pd/C) is preferably used. The palladium catalyst is used in an amount of 0.001-1 equivalents, preferably 0.005-0.5 equivalents, relative to compound (XX).

(184) The reaction temperature is generally 40-150 C., preferably 20-110 C. While the reaction time is appropriately selected according to the conditions such as reaction temperature and the like, it is generally about 20 min-48 hr. While the concentration of substrate (XX) in the reaction system is not particularly limited, it is generally preferably 0.001 mmol/L-1 mol/L.

(185) The deprotection of the tert-butoxycarbonyl (Boc) group can be performed by a method similar to Scheme 1, Step 2.

(186) Step 4

(187) Compound (XXIII) can be obtained by, for example, amidation of amine compound (XXI) with acyl halide (XXII) wherein X.sup.1 is a halogen atom or carboxylic acid (XXII) wherein X.sup.1 is a hydroxy group.

(188) Amidation can be performed by a method similar to Scheme 1, Step 3.

(189) Step 5

(190) Compound (I-12) can be obtained by, for example, reacting compound (XXIII) with para-formaldehyde.

(191) As the solvent, carboxylic acid solvents such as acetic acid and the like can be used. Para-formaldehyde is used in an amount of 1.0-20 equivalents, preferably 1.0-10 equivalents, relative to compound (XXIII).

(192) The reaction temperature is generally 40-150 C., preferably 0-80 C. While the reaction time is appropriately selected according to the conditions such as reaction temperature and the like, it is generally about 20 min-48 hr. While the concentration of substrate (XXIII) in the reaction system is not particularly limited, it is generally preferably 0.001 mmol/L-1 mol/L.

(193) ##STR00030##
wherein R.sup.1, R.sup.2, R.sup.3, R.sup.4, X and W are as defined above.

(194) Compound (I) can be obtained by, for example, amidation of sulfonyl chloride compound (II) with amine compound (XXIV).

(195) Amidation can be performed by a method similar to Scheme 1, Step 1.

(196) ##STR00031##
wherein R.sup.1, R.sup.12, X and W are as defined above.

(197) Compound (I-13) can be obtained by, for example, diazotization of amine compound (V) and subjecting the obtained diazonium salt to a diazocoupling reaction with compound (XXV).

(198) The diazotization can be performed by reacting amine compound (V) with a nitrite salt such as sodium nitrite and the like in an aqueous acidic solution. The nitrite salt is used in an amount of 1.0-20 equivalents, preferably 1.0-10 equivalents, relative to amine compound (V).

(199) The diazocoupling reaction can be performed by reacting the obtained diazonium salt with compound (XXV). The compound (XXV) is used in an amount of 1.0-20 equivalents, preferably 1.0-10 equivalents, relative to amine compound (V).

(200) The reaction temperature is generally 40-150 C., preferably 0-80 C. While the reaction time is appropriately selected according to the conditions such as reaction temperature and the like, it is generally about 20 min-48 hr. While the concentration of substrate (V) in the reaction system is not particularly limited, it is generally preferably 0.001 mmol/L-1 mol/L.

(201) ##STR00032##
wherein R.sup.1, X and W are as defined above, R.sup.13a is C.sub.1-6 alkyl, C.sub.6-10 aryl-C.sub.1-6 alkyl or C.sub.2-6 alkenyl-carbonyl and R.sup.14a is C.sub.1-6 alkyl optionally substituted by one substituent selected from (a) C.sub.1-6 alkoxy-carbonylamino, (b) C.sub.2-6 alkenyl-carbonylamino and (c) C.sub.6-10 aryl-C.sub.1-6 alkylaminocarbonyl optionally substituted by C.sub.1-6 alkyl.

(202) Compound (I-14) can be obtained, for example, by acylation and/or alkylation of amine compound (V).

(203) Acylation can be performed by a method similar to Scheme 1, Step 3. Alkylation can be performed by a method similar to the reductive alkylation of Scheme 2.

(204) ##STR00033##
wherein R.sup.1, R.sup.7, R.sup.Wa, R.sup.Wb and X are as defined above.
Step 1

(205) Compound (XXVII) can be obtained by, for example, reacting compound (XXVI) with isocyanate (IX), and deprotecting the tert-butoxycarbonyl (Boc) group of the obtained compound.

(206) The reaction of compound (XXVI) and isocyanate (IX) can be performed by a method similar to Scheme 4. The deprotection of the tert-butoxycarbonyl (Boc) group can be performed by a method similar to Scheme 1, Step 2.

(207) Step 2

(208) Compound (XXIX) can be obtained, for example, by amidation of compound (XXVII) with sulfonyl chloride compound (XXX).

(209) Amidation can be performed by a method similar to Scheme 1, Step 1.

(210) Step 3

(211) Compound (I-15) can be obtained, for example, by amidation of compound (XXIX) with amine compound (XXX).

(212) Amidation can be performed by a method similar to Scheme 11, Step 4.

(213) ##STR00034##
wherein R.sup.1, R.sup.2, R.sup.3, R.sup.4, X and W are as defined above.
Step 1

(214) Compound (XXXI) can be obtained, for example, by amidation of sulfonyl chloride compound (XVI) with compound (XXIV).

(215) Amidation can be performed by a method similar to Scheme 1, Step 1.

(216) Step 2

(217) Compound (I) can be obtained, for example, by Suzuki coupling of compound (XXXI) with boronic acid compound (XIX).

(218) The Suzuki coupling can be performed by a method similar to Scheme 11, Step 2.

(219) ##STR00035##
wherein R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.Wa, R.sup.Wb and X are as defined above.

(220) Compound (I-16) can be obtained, for example, by amidation of compound (XXXII) with amine compound (XXX).

(221) Amidation can be performed by a method similar to Scheme 11, Step 4.

(222) ##STR00036##
wherein R.sup.1, R.sup.6a, R.sup.15, R.sup.16 and X are as defined above.
Step 1

(223) Compound (I) can be obtained, for example, by amidation of sulfonyl chloride compound (XXXIII) with compound (XXXIV).

(224) Amidation can be performed by a method similar to Scheme 1, Step 1.

(225) Step 2

(226) Compound (XXXV) can be obtained, for example, by amidation of sulfonyl chloride compound (XVI) with compound (XXXIV).

(227) Amidation can be performed by a method similar to Scheme 1, Step 1.

(228) Step 3

(229) Compound (I) can be obtained, for example, by Suzuki coupling of compound (XXXV) with boronic acid compound (XXXVI).

(230) The Suzuki coupling can be performed by a method similar to Scheme 11, Step 2.

(231) Compound (I) wherein R.sup.3 is R.sup.6, and R.sup.2 and R.sup.4 are each a hydrogen atom can be obtained by a method similar to one mentioned above by using the following amine compound (III-1) instead of amine compound (III).

(232) Compound (I) wherein R.sup.4 is R.sup.6, and R.sup.2 and R.sup.3 are each a hydrogen atom can be obtained by a method similar to one mentioned above by using the following amine compound (III-2) instead of amine compound (III).

(233) ##STR00037##
wherein X are as defined above.

(234) An orexin receptor agonist containing the compound of the present invention is effective for not only human but also mammals other than human, for example, mouse, rat, hamster, rabbit, cat, dog, bovine, sheep, monkey and the like.

(235) Also, the compound of the present invention is used not only as an agent for the prophylaxis or treatment of narcolepsy as mentioned above but also can be used in a method of preventing or treating narcolepsy, or for the production of a medicament for the prophylaxis or treatment of narcolepsy.

(236) Furthermore, the compound of the present invention can also be used as an agent for improving sleepiness, or a prophylactic or therapeutic agent for obesity, diabetes, depression, sepsis, severe sepsis, septic shock and the like.

(237) When the compound of the present invention is clinically used as an agent for the prophylaxis or treatment of narcolepsy, an agent for improving sleepiness or a prophylactic or therapeutic agent for obesity, diabetes, depression, sepsis, severe sepsis, septic shock and the like, the medicament may be a free form of the compound of the present invention or an acid addition salt thereof, or additives such as excipient, stabilizer, preservative, buffering agent, solubilizing agent, emulsifier, diluent, isotonicity agent and the like may be mixed as appropriate. Examples of the administration form include oral preparations such as tablet, capsule, granule, powder, syrup and the like, parenteral agents such as injection, suppository, liquid and the like, topical administration of ointment, cream, adhesive preparation and the like, and the like.

(238) The agent for the prophylaxis or treatment of narcolepsy, the agent for improving sleepiness, or the prophylactic or therapeutic agent for obesity, diabetes, depression, sepsis, severe sepsis, septic shock and the like of the present invention desirably contains 0.001-90 wt %, preferably 0.01-70 wt %, of the above-mentioned active ingredient. The amount thereof to be used is appropriately determined according to the symptom, age, body weight, and administration method. In the case of injection for an adult, the amount of the active ingredient is 0.1 g-1 g per day, 1 g-1 g in the case of an oral preparation, and 1 g-10 g in the case of an adhesive preparation, each of which can be administered in one to several portions.

(239) In addition, the agent for the prophylaxis or treatment of narcolepsy or the agent for improving sleepiness of the present invention can also be used in combination with an agent for the prophylaxis or treatment of strong sleepiness and dozing during the day, an agent for the prophylaxis or treatment of deep sleep disorder, or an agent for the prophylaxis or treatment of cataplexy.

(240) As an agent for the prophylaxis or treatment of strong sleepiness and dozing during the day, central nervous system stimulants such as methylphenidate, pemoline, modafinil and the like, and the like can be mentioned.

(241) As an agent for the prophylaxis or treatment of deep sleep disorder, sleep inducing drugs such as triazolam, vegetamin B and the like, antianxiety drug and the like can be mentioned.

(242) As an agent for the prophylaxis or treatment of cataplexy, tricyclic antidepressants such as clomipramine hydrochloride, brotizolam, imipramine hydrochloride and the like, selective serotonin reuptake inhibitors (SSRI) such as fluvoxamine maleate, paroxetine, hydrochloride and the like, serotonin and noradrenaline reuptake inhibitors (SNRI) such as milnacipran hydrochloride, duloxetine hydrochloride and the like, and the like can be mentioned.

EXAMPLES

(243) The present invention is specifically explained in the following by referring to Examples. In the following Examples, the following abbreviations are used. Boc: tert-butoxycarbonyl Bn: benzyl DIPEA: N,N-diisopropylethylamine DME: 1,2-dimethoxyethane DMF: N,N-dimethylformamide DPPA: diphenylphosphoryl azide HATU: O-(7-azabenzotriazol-1-yl)-N,N,N,N-tetramethyluronium hexafluorophosphate IBX: 2-iodoxybenzoic acid BOP: benzotriazol-1-yloxytris(dimethylamino)phosphonium hexafluorophosphate Me: methyl Ph: phenyl TEA: triethylamine TFA: 2,2,2-trifluoroacetic acid

(244) Compound names were determined using ChemBioDraw Ultra ver.12.0.3 of Cambridge Corporation.

(245) The room temperature in the following Examples and Production Examples mean generally from about 10 C. to about 35 C. Unless particularly indicated, % shows weight percent.

Production Example (1)

(246) ##STR00038##

(1) 3-(dimethylcarbamoyl)-4-methoxy-[1,1-biphenyl]-3-sulfonyl chloride

(247) ##STR00039## (i) Under an argon atmosphere, to a solution of 4-bromoanisole (1.0 mL) in DME (20.0 mL) were added 3-(N,N-dimethylaminocarbonyl)phenylboronic acid (1.60 g), sodium carbonate (1.80 g), water (2.0 mL) and tetrakis(triphenylphosphine)palladium (250.0 mg), and the mixture was heated under reflux overnight. The reaction mixture was filtered through celite, and the filtrate was concentrated. To the obtained residue was added pure water and the mixture was extracted with chloroform. The organic layer was dried over sodium sulfate and filtered, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (eluent: ethyl acetate/hexane=1/2.fwdarw.1/1) to give 4-methoxy-N,N-dimethyl-[1,1-biphenyl]-3-carboxamide (1.72 g). (ii) Under an argon atmosphere, to chlorosulfonic acid (870 L) was slowly added a solution of 4-methoxy-N,N-dimethyl-[1,1-biphenyl]-3-carboxamide (1.10 g) in dichloromethane (4.0 mL), and the mixture was stirred under ice-cooling for 10 min. The reaction mixture was warmed to room temperature and stirred for 2 hr. Thionyl chloride (950 L) and DMF (1.70 mL) were added, and the mixture was stirred at room temperature overnight. The reaction mixture was poured into ice and the mixture was stirred for 1 hr and extracted with chloroform. The organic layer was dried over sodium sulfate and filtered, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (eluent: ethyl acetate/hexane=1/1.fwdarw.1/0) to give 3-(dimethylcarbamoyl)-4-methoxy-[1,1-biphenyl]-3-sulfonyl chloride (1.40 g).

(2) tert-butyl (3-(3-(dimethylcarbamoyl)-4-methoxy-[1,1-biphenyl]-3-ylsulfonamido)phenyl)carbamate

(248) ##STR00040##

(249) Under an argon atmosphere, to a solution of tert-butyl (3-aminophenyl)carbamate (1.22 g) in dichloromethane (4.0 mL) was added a solution of DIPEA (2.80 mL) and 3-(dimethylcarbamoyl)-4-methoxy-[1,1-biphenyl]-3-sulfonyl chloride (1.88 g) in dichloromethane (4.0 mL), and the mixture was stirred at room temperature for 4 hr. The resulting white solid was collected by filtration, and the residue was washed with 25% dichloromethane-containing hexane solution. The filtrate was concentrated under reduced pressure, 25% dichloromethane-containing hexane solution was added and the resulting white solid was similarly collected by filtration and washed. The obtained solid was dried in vacuo to give tert-butyl (3-(3-(dimethylcarbamoyl)-4-methoxy-[1,1-biphenyl]-3-ylsulfonamido)phenyl)carbamate (2.51 g).

(3) 3-(N-(3-aminophenyl)sulfamoyl)-4-methoxy-N,N-dimethyl-[1,1-biphenyl]-3-carboxamide hydrochloride

(250) ##STR00041##

(251) To a suspension of tert-butyl (3-(3-(dimethylcarbamoyl)-4-methoxy-[1,1-biphenyl]-3-ylsulfonamido)phenyl)carbamate (2.42 g) in diethyl ether (18.8 mL) was added 10% hydrogen chloride-methanol solution (47.0 mL), and the mixture was stirred at 60 C. for 12 hr. The resulting white solid was collected by filtration, and washed with diethyl ether. The filtrate was concentrated under reduced pressure and diethyl ether was added to the residue. The resulting white solid was similarly collected by filtration and washed. The obtained solid was dried in vacuo to give 3-(N-(3-aminophenyl)sulfamoyl)-4-methoxy-N,N-dimethyl-[1,1-biphenyl]-3-carboxamide hydrochloride (1.99 g).

(4) 3-(N-(3-benzamidophenyl)sulfamoyl)-4-methoxy-N,N-dimethyl-[1,1-biphenyl]-3-carboxamide

(252) ##STR00042##

(253) Under an argon atmosphere, to a solution of 3-(N-(3-aminophenyl)sulfamoyl)-4-methoxy-N,N-dimethyl-[1,1-biphenyl]-3-carboxamide hydrochloride (20.0 mg) in anhydrous pyridine (1.0 mL) was added benzoyl chloride (6.03 g) under ice-cooling, and the mixture was warmed to room temperature and stirred for 5 hr. The reaction mixture was diluted with ethyl acetate, and extracted with 1 M aqueous hydrochloric acid solution. The organic layer was washed with saturated aqueous sodium hydrogen carbonate solution and saturated brine, dried over sodium sulfate and filtered, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (eluent: hexane/ethyl acetate=1/0.fwdarw.20/1) to give 3-(N-(3-benzamidophenyl)sulfamoyl)-4-methoxy-N,N-dimethyl-[1,1-biphenyl]-3-carboxamide (21.8 mg).

(254) The compounds described in the following Tables 1 and 2 were also synthesized similarly from acid chloride or carboxylic acid having the corresponding R group.

(255) ##STR00043##

(256) TABLE-US-00001 TABLE 1 Ex. No. NHCOR moiety structure .sup.1H-NMR 1 1H NMR (400 MHz, Pyridine-d5) 12.13 (brs, 1H), 11.03 (brs, 1H), 8.83 (dd, J = 2.0 Hz, 1H), 8.67 (d, J = 2.4 Hz, 1H), 8.13-8.07 (m, 2H), 7.83 (dd, J = 1.5 Hz, 1H), 7.67 (dd, J = 8.6, 2.4 Hz, 1H), 7.60 (dd, J = 8.5 Hz, 2H), 7.51 (d, J = 7.6 Hz, 2H), 7.45-7.32 (m, 4H), 7.27 (dd, J = 8.1 Hz, 1H), 7.09 (d, J = 8.7 Hz, 1H), 3.72 (s, 3H), 3.05 (brs, 3H), 2.79 (brs, 3H). 2 1H NMR (400 MHz, Chloroform-d) 8.04 (d, J = 2.4 Hz, 1H), 7.70 (dd, J = 8.6, 2.4 Hz, 1H), 7.66 (s, 1H), 7.62-7.58 (m, 2H), 7.56 (dd, J = 7.7, 1.4 Hz, 1H), 7.54-7.51 (m, 2H), 7.42 (dd, J = 48.2, 7.8 Hz, 1H), 7.37 (t, J = 7.4 Hz, 1H), 7.35-7.27 (m, 2H), 7.21-7.16 (m, 2H), 7.09 (d, J = 8.7 Hz, 1H), 7.05 (s, 1H), 7.02-6.95 (m, 1H), 4.12 (s, 4H), 3.09 (s, 3H), 2.98 (s, 3H). 3 1H NMR (400 MHz, Chloroform-d) 8.04 (d, J = 2.4 Hz, 1H), 7.93 (d, J = 8.7 Hz, 1H), 7.85 (s, 1H), 7.71-7.65 (m, 3H), 7.62-7.56 (m, 3H), 7.54-7.49 (m, 2H), 7.44-7.38 (m, 1H), 7.35- 7.30 (m, 1H), 7.19 (t, J = 8.0 Hz, 1H), 7.08 (d, J = 8.6 Hz, 1H), 7.05 (s, 1H), 6.89 (ddd, J = 7.9, 2.0, 0.9 Hz, 1H), 4.11 (s, 3H), 3.10 (s, 3H), 2.97 (s, 3H). 4 1H NMR (400 MHz, Chloroform-d) 8.77 (d, J = 6.0 Hz, 2H), 8.08 (d, J = 0.5 Hz, 1H), 8.04 (d, J = 2.4 Hz, 1H), 8.02 (brs, 1H), 7.70 (dd, J = 8.6, 2.1 Hz, 1H), 7.66 (d, J = 6.2 Hz, 2H), 7.58 (dd, J = 2.1 Hz, 1H), 7.55-7.50 (m, 2H), 7.41 (dd, J = 7.9 Hz, 1H), 7.35-7.30 (m, 1H), 7.20 (dd, J = 8.0 Hz, 1H), 7.09 (d, J = 8.6 Hz, 1H), 7.05 (brs, 1H), 6.93-6.87 (m, 1H), 4.11 (s, 3H), 3.10 (s, 3H), 2.98 (s, 3H). 5 1H NMR (400 MHz, Methanol-d4) 8.11 (d, J = 2.4 Hz, 1H), 7.83-7.77 (m, 2H), 7.67 (d, J = 8.0 Hz, 1H), 7.60 (dd, J = 1.6 Hz, 1H), 7.53-7.44 (m, 2H), 7.38 (dt, J = 7.6, 1.2 Hz, 1H), 7.35 (d, J = 1.8 Hz, 1H), 7.24-7.13 (m, 3H), 6.95- 6.89 (m, 2H), 6.06 (s, 2H), 4.04 (s, 3H), 3.11 (s, 3H), 3.01 (s, 3H). 6 1H NMR (400 MHz, Chloroform-d) 12.30 (s, 1H), 8.20 (dd, J = 7.8, 1.6 Hz, 1H), 8.07 (d, J = 2.3 Hz, 1H), 7.73-7.66 (m, 3H), 7.54 (dd, J = 4.2, 2.4 Hz, 3H), 7.51-7.45 (m, 1H), 7.42 (t, J = 8.0 Hz, 1H), 7.34 (d, J = 7.6 Hz, 1H), 7.29 (d, J = 7.3 Hz, 1H), 7.18 (d, J = 5.2 Hz, 1H), 7.09 (d, J = 8.7 Hz, 1H), 7.02 (s, 1H), 6.94 (td, J = 4.1, 2.1 Hz, 1H), 4.15 (s, 3H), 3.11 (s, 3H), 2.97 (s, 3H), 2.76 (s, 6H). 7 0 1H NMR (400 MHz, DMSO-d6) 10.14 (brs, 1H), 10.09 (s, 1H), 8.04 (d, J = 2.4 Hz, 1H), 7.90 (dd, J = 8.7, 2.4 Hz, 1H), 7.77 (dd, J = 1.9 Hz, 1H), 7.71 (ddd, J = 7.8, 1.4 Hz, 1H), 7.60 (dd, J = 1.6 Hz, 1H), 7.47 (dd, J = 7.7 Hz, 1H), 7.35 (ddd, J = 7.6, 1.2 Hz, 1H), 7.33-7.25 (m, 3H), 7.16-7.10 (m, 3H), 6.93- 6.87 (m, 1H), 6.84 (ddd, J = 8.1, 2.0, 0.8 Hz, 1H), 3.95 (s, 3H), 2.96 (s, 3H), 2.93 (s, 6H), 2.87 (s, 3H). 8 1H NMR (400 MHz, Chloroform-d) 8.03 (s, 1H), 7.75-7.63 (m, 4H), 7.59- 7.49 (m, 3H), 7.41 (t, J = 7.7 Hz, 1H), 7.35-7.30 (m, 1H), 7.22 (s, 1H), 7.16 (t, J = 8.6 Hz, 1H), 7.08 (d, J = 8.8 Hz, 1H), 6.99 (s, 1H), 6.89 (d, J = 7.5 Hz, 1H), 6.73-6.63 (m, 2H), 4.12 (s, 3H), 3.11 (s, 3H), 3.03 (s, 6H), 2.98 (s, 3H). 9 1H NMR (400 MHz, DMSO-d6) 10.40 (s, 1H), 10.16 (s, 1H), 8.50 (s, 1H), 8.12- 7.97 (m, 4H), 7.94 (dd, J = 8.6, 1.8 Hz, 1H), 7.91 (dd, J = 8.7, 2.4 Hz, 1H), 7.85 (t, J = 2.0 Hz, 1H), 7.73 (ddd, J = 7.8, 1.8, 1.1 Hz, 1H), 7.68-7.59 (m, 3H), 7.48 (t, J = 7.7 Hz, 1H), 7.39 (ddd, J = 8.1, 1.9, 0.8 Hz, 1H), 7.35 (ddd, J = 7.6, 1.3 Hz, 1H), 7.28 (d, J = 8.8 Hz, 1H), 7.17 (t, J = 8.1 Hz, 1H), 6.87 (ddd, J = 8.1, 2.1, 0.9 Hz, 1H), 3.97 (s, 3H), 2.92 (s, 3H), 2.85 (s, 3H). 10 1H NMR (400 MHz, Chloroform-d) 8.31- 8.22 (m, 1H), 8.06 (d, J = 2.4 Hz, 1H), 7.95 (d, J = 8.3 Hz, 1H), 7.92-7.85 (m, 1H), 7.71 (ddd, J = 16.9, 12.1, 8.1 Hz, 4H), 7.60-7.51 (m, 4H), 7.48 (p, J = 8.1, 7.1 Hz, 1H), 7.41 (t, J = 8.0 Hz, 1H), 7.33 (dt, J = 7.5, 1.3 Hz, 1H), 7.25-7.21 (m, 2H), 7.15-7.07 (m, 2H), 7.01 (ddd, J = 7.3, 2.1 Hz, 1H), 4.15 (s, 3H), 3.08 (s, 3H), 2.97 (s, 3H).

(257) TABLE-US-00002 TABLE 2 Ex. No. NHCOR moiety structure .sup.1H-NMR 11 1H NMR (400 MHz, DMSO-d6) 10.29 (s, 1H), 10.18 (s, 1H), 8.67 (d, J = 4.8 Hz, 1H), 8.15 (d, J = 7.9 Hz, 1H), 8.06 (d, J = 2.3 Hz, 1H), 8.00 (ddd, J = 7.8, 1.7 Hz, 1H), 7.91 (dd, J = 8.6, 2.3 Hz, 1H), 7.72 (d, J = 7.8 Hz, 1H), 7.69-7.60 (m, 2H), 7.59-7.53 (m, 1H), 7.51 (t, J = 7.7 Hz, 1H), 7.38-7.33 (m, 1H), 7.32- 7.25 (m, 2H), 7.15 (dd, J = 8.1 Hz, 1H), 6.87 (d, J = 7.7 Hz, 1H), 3.95 (s, 3H), 3.17 (d, J = 5.0 Hz, 3H), 2.95 (s, 3H), 2.89 (s, 3H). 12 1H NMR (400 MHz, Chloroform-d) 8.73 (s, 1H), 8.72 (s, 1H), 8.06 (d, J = 2.4 Hz, 1H), 7.82-7.73 (m, 3H), 7.71 (dd, J = 8.6, 2.4 Hz, 1H), 7.56-7.50 (m, 3H), 7.41 (dd, J = 8.0 Hz, 1H), 7.34- 7.27 (m, 2H), 7.21 (dd, J = 8.2 Hz, 1H), 7.17-7.06 (m, 2H), 6.94-6.87 (m, 1H), 4.11 (s, 3H), 3.11 (s, 3H), 2.98 (s, 3H), 2.75 (s, 3H). 13 1H NMR (400 MHz, Chloroform-d): 9.09 (s, 1H), 8.06 (d, J = 2.8 Hz, 1H), 7.67 (dd, J = 2.8, 8.0 Hz, 1H), 7.55-7.50 (m, 2H), 7.48-7.29 (m, 12H), 7.10 (t, J = 8.0 Hz, 1H), 7.03-6.97 (m, 3H), 5.18 (s, 1H), 3.99 (s, 3H), 3.59 (d, J = 14.0 Hz, 1H), 3.25 (d, J = 14.0 Hz, 1H), 3.11 (s, 3H), 2.96 (s, 3H), 1.61 (brs, 2H). 14 1H NMR (400 MHz, Pyridine-d5) 12.12 (brs, 1H), 10.96 (s, 1H), 8.83 (t, J = 1.9 Hz, 1H), 8.70 (d, J = 2.4 Hz, 1H), 7.98 (d, J = 15.6 Hz, 1H), 7.96 (s, 1H), 7.91 (dd, J = 1.5 Hz, 1H), 7.68 (dd, J = 8.6, 2.4 Hz, 1H), 7.63-7.59 (m, 1H), 7.56-7.49 (m, 3H), 7.43 (dd, J = 7.7 Hz, 1H), 7.39 (ddd, J = 8.1, 2.0, 0.9 Hz, 1H), 7.23 (dd, J = 8.1 Hz, 1H), 7.08 (d, J = 8.7 Hz, 1H), 6.66 (d, J = 15.4 Hz, 1H), 6.49 (brd, J = 1.9 Hz, 1H), 3.71 (s, 3H), 3.06 (brs, 3H), 2.80 (brs, 3H). 15 1H NMR (400 MHz, Chloroform-d) 8.04 (d, J = 2.4 Hz, 1H), 7.90 (s, 1H), 7.69 (dd, J = 8.6, 2.4 Hz, 1H), 7.63 (brs, 1H), 7.62-7.56 (m, 2H), 7.55-7.49 (m, 2H), 7.41 (dd, J = 8.3 Hz, 1H), 7.36- 7.31 (m, 2H), 7.29 (ddd, J = 8.6, 2.1, 0.9 Hz, 1H), 7.18 (dd, J = 8.1 Hz, 1H), 7.13 (brs, 1H), 7.08 (d, J = 8.7 Hz, 1H), 6.93 (ddd, J = 8.0, 2.1, 0.9 Hz, 1H), 4.12 (s, 3H), 3.11 (s, 3H), 2.97 (s, 3H), 2.40 (s, 3H). 16 1H NMR (400 MHz, Chloroform-d) 8.03 (d, J = 2.4 Hz, 1H), 7.75 (brs, 1H), 7.68 (dd, J = 8.6, 2.4 Hz, 1H), 7.58 (brs, 1H), 7.55-7.50 (m, 2H), 7.44- 7.34 (m, 2H), 7.34-7.28 (m, 2H), 7.26- 7.22 (m, 2H), 7.22-7.12 (m, 3H), 7.07 (d, J = 8.7 Hz, 1H), 6.98-6.92 (m, 1H), 4.09 (s, 3H), 3.08 (s, 3H), 2.97 (s, 3H), 2.40 (s, 3H). 17 0 1H NMR (400 MHz, Pyridine-d5) 12.13 (brs, 1H), 10.96 (brs, 1H), 8.86 (dd, J = 2.0 Hz, 1H), 8.67 (d, J = 2.4 Hz, 1H), 8.06 (d, J = 8.2 Hz, 2H), 7.83 (dd, J = 1.7 Hz, 1H), 7.67 (dd, J = 8.6, 2.4 Hz, 1H), 7.62 (ddd, J = 7.7, 1.5 Hz, 1H), 7.58 (ddd, J = 8.0, 2.1, 0.9 Hz, 1H), 7.53-7.48 (m, 2H), 7.42 (dd, J = 7.6 Hz, 1H), 7.26 (dd, J = 8.1 Hz, 1H), 7.15 (d, J = 7.9 Hz, 2H), 7.08 (d, J = 8.7 Hz, 1H), 3.73 (s, 3H), 3.05 (brs, 3H), 2.79 (brs, 3H), 2.17 (s, 3H). 18 1H NMR (400 MHz, Pyridine-d5) 12.07 (brs, 1H), 10.44 (brs, 1H), 8.75 (dd, J = 2.0 Hz, 1H), 8.63 (d, J = 2.4 Hz, 1H), 8.12 (dd, J = 7.7, 1.8 Hz, 1H), 7.77 (dd, J = 1.6 Hz, 1H), 7.60 (dd, J = 8.6, 2.4 Hz, 1H), 7.55 (ddd, J = 7.7, 1.9, 1.2 Hz, 1H), 7.49 (ddd, J = 8.0, 2.1, 1.0 Hz, 1H), 7.43 (ddd, J = 7.6, 1.3 Hz, 1H), 7.34 (dd, J = 7.6 Hz, 1H), 7.30 (ddd, J = 7.2, 1.9, 1.8 Hz, 1H), 7.26 (ddd, J = 8.0, 1.9, 1.0 Hz, 1H), 7.17 (dd, J = 8.0 Hz, 1H), 7.01 (d, J = 8.7 Hz, 1H), 6.98 (ddd, J = 7.7, 1.1 Hz, 2H), 3.64 (s, 3H), 3.57 (s, 3H), 2.97 (s, 3H), 2.72 (s, 3H). 19 1H NMR (400 MHz, Pyridine-d5) 12.13 (brs, 1H), 10.89 (s, 1H), 8.86 (dd, J = 2.0 Hz, 1H), 8.68 (d, J = 2.4 Hz, 1H), 8.19 (d, J = 8.9 Hz, 2H), 7.84 (dd, J = 1.5 Hz, 1H), 7.67 (dd, J = 8.6, 2.4 Hz, 1H), 7.65-7.60 (m, 1H), 7.57 (ddd, J = 8.1, 2.1, 0.9 Hz, 1H), 7.54-7.47 (m, 2H), 7.43 (dd, J = 7.6 Hz, 1H), 7.26 (dd, J = 8.1 Hz, 1H), 7.08 (d, J = 8.7 Hz, 1H), 6.99 (d, J = 8.9 Hz, 2H), 3.73 (s, 3H), 3.64 (s, 3H), 3.05 (s, 3H), 2.79 (s, 3H).

Production Example (2)

(258) ##STR00063##

(1) 3-(N-(3-(benzylamino)phenyl)sulfamoyl)-4-methoxy-N,N-dimethyl-[1,1-biphenyl]-3-carboxamide

(259) ##STR00064##

(260) Under an argon atmosphere, to a suspension of 3-(N-(3-aminophenyl)sulfamoyl)-4-methoxy-N,N-dimethyl-[1,1-biphenyl]-3-carboxamide hydrochloride (10.0 mg) in dichloromethane (215 L) were added TEA (3.0 L), acetic acid (5.0 L) and benzaldehyde (2.25 L), and the mixture was stirred at room temperature for 3.5 hr. Thereto was added sodium triacetoxyborohydride (10 mg), and the mixture was stirred for 14 hr. The reaction mixture was diluted with ethyl acetate, and extracted with 1 M aqueous hydrochloric acid solution. The organic layer was washed with saturated aqueous sodium hydrogen carbonate solution and saturated brine, dried over sodium sulfate and filtered, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (eluent: ethyl acetate/hexane=0/1.fwdarw.20/1) to give 3-(N-(3-(benzylamino)phenyl)sulfamoyl)-4-methoxy-N,N-dimethyl-[1,1-biphenyl]-3-carboxamide (21.8 mg).

(261) The compounds described in the following Table 3 were also synthesized similarly from aldehyde having the corresponding R group.

(262) ##STR00065##

(263) TABLE-US-00003 TABLE 3 Ex. No. NHCH.sub.2R moiety structure .sup.1H-NMR 20 1H NMR (400 MHz, Chloroform-d) 8.03 (d, J = 2.3 Hz, 1H), 7.68 (dd, J = 8.6, 2.4 Hz, 1H), 7.61-7.49 (m, 2H), 7.43 (dd, J = 7.6 Hz, 1H), 7.39-7.33 (m, 1H), 7.31-7.21 (m, 5H), 7.01 (d, J = 8.5 Hz, 1H), 6.94 (dd, J = 8.0 Hz, 1H), 6.88 (s, 1H), 6.45-6.39 (m, 1H), 6.39-6.27 (m, 2H), 4.21 (s, 2H), 4.07 (brs, 1H), 3.96 (s, 3H), 3.12 (s, 3H), 2.98 (s, 3H). 21 1H NMR (400 MHz, Chloroform-d) 8.06 (d, J = 2.3 Hz, 1H), 7.69 (dd, J = 8.6, 2.4 Hz, 1H), 7.58-7.50 (m, 2H), 7.43 (dd, J = 7.6 Hz, 1H), 7.35 (ddd, J = 7.5, 1.2 Hz, 1H), 7.19 (d, J = 8.5 Hz, 2H), 7.08 (s, 1H), 7.02 (d, J = 8.7 Hz, 1H), 6.95 (dd, J = 8.0 Hz, 1H), 6.82 (d, J = 8.6 Hz, 2H), 6.43 (dd, J = 2.1 Hz, 1H), 6.39 (dd, J = 7.8, 1.8 Hz, 1H), 6.30 (dd, J = 8.1, 2.2 Hz, 1H), 4.13 (s, 2H), 3.99 (s, 3H), 3.77 (s, 3H), 3.12 (s, 3H), 2.98 (s, 3H). 22 1H NMR (400 MHz, Chloroform-d) 8.05 (d, J = 2.4 Hz, 1H), 7.68 (dd, J = 8.6, 2.4 Hz, 1H), 7.57-7.49 (m, 2H), 7.43 (dd, J = 7.6 Hz, 1H), 7.35 (d, J = 7.6 Hz, 1H), 7.23-7.13 (m, 2H), 7.03 (s, 1H), 6.99 (d, J = 8.6 Hz, 1H), 6.93 (dd, J = 8.0 Hz, 1H), 6.87-6.78 (m, 2H), 6.43 (dd, J = 2.1 Hz, 1H), 6.37 (dd, J = 7.9, 2.0 Hz, 1H), 6.32 (dd, J = 8.2, 2.3 Hz, 1H), 4.21 (s, 2H), 3.96 (s, 3H), 3.81 (s, 3H), 3.12 (s, 3H), 2.98 (s, 3H). 23 1H NMR (400 MHz, Chloroform-d) 8.04 (d, J = 2.4 Hz, 1H), 7.67 (dd, J = 8.6, 2.4 Hz, 1H), 7.57-7.49 (m, 2H), 7.42 (dd, J = 7.6 Hz, 1H), 7.34 (ddd, J = 7.5, 1.3 Hz, 1H), 7.18 (dd, J = 7.8 Hz, 1H), 7.02 (s, 1H), 6.99 (d, J = 8.7 Hz, 1H), 6.93 (dd, J = 8.3 Hz, 1H), 6.86- 6.79 (m, 2H), 6.76 (dd, J = 8.2, 2.5 Hz, 1H), 6.42-6.37 (m, 2H), 6.32-6.27 (m, 1H), 4.18 (s, 2H), 4.07 (d, J = 17.4 Hz, 1H), 3.95 (s, 3H), 3.73 (s, 3H), 3.11 (s, 3H), 2.97 (s, 3H). 24 0 1H NMR (400 MHz, Chloroform-d) 8.04 (d, J = 2.4 Hz, 1H), 7.69 (dd, J = 8.6, 2.4 Hz, 1H), 7.59-7.49 (m, 2H), 7.42 (dd, J = 7.9 Hz, 1H), 7.35 (ddd, J = 7.5, 1.4 Hz, 1H), 7.20 (d, J = 7.6 Hz, 1H), 7.18-7.14 (m, 2H), 7.12- 7.06 (m, 1H), 7.01 (d, J = 8.7 Hz, 1H), 6.96 (dd, J = 8.0 Hz, 1H), 6.85 (s, 1H), 6.40 (dd, J = 2.1 Hz, 1H), 6.37 (ddd, J = 7.8, 2.0, 0.8 Hz, 1H), 6.31 (ddd, J = 8.2, 2.3, 0.8 Hz, 1H), 4.15 (s, 2H), 3.97 (s, 3H), 3.88 (s, 1H), 3.12 (s, 3H), 2.98 (s, 3H), 2.28 (s, 3H). 25 1H NMR (400 MHz, Chloroform-d) 8.06 (d, J = 2.4 Hz, 1H), 7.68 (dd, J = 8.6, 2.4 Hz, 1H), 7.58-7.55 (m, 1H), 7.55-7.50 (m, 1H), 7.43 (dd, J = 7.6 Hz, 1H), 7.35 (ddd, J = 7.5, 1.4 Hz, 1H), 7.17 (dd, J = 7.5 Hz, 1H), 7.10 (s, 2H), 7.05 (t, J = 6.8 Hz, 2H), 7.01 (d, J = 8.7 Hz, 1H), 6.95 (t, J = 8.0 Hz, 1H), 6.45- 6.37 (m, 2H), 6.31 (ddd, J = 8.2, 2.3, 0.9 Hz, 1H), 4.16 (s, 2H), 3.96 (s, 3H), 3.13 (s, 3H), 2.98 (s, 3H), 2.30 (s, 3H). 26 1H NMR (400 MHz, Chloroform-d) 8.43 (brs, 1H), 8.06 (d, J = 2.4 Hz, 1H), 7.66 (dd, J = 8.6, 2.4 Hz, 1H), 7.59 (dd, J = 1.3 Hz, 1H), 7.53 (d, J = 7.8 Hz, 1H), 7.42 (dd, J = 7.6 Hz, 1H), 7.32 (d, J = 7.7 Hz, 1H), 7.12-7.05 (m, 2H), 7.04-6.93 (m, 3H), 6.83-6.73 (m, 2H), 6.57 (dd, J = 2.0 Hz, 1H), 6.44-6.32 (m, 2H), 4.16 (s, 2H), 3.96 (s, 3H), 3.16 (s, 3H), 3.03 (s, 3H). 27 1H NMR (400 MHz, Chloroform-d) 8.05 (d, J = 2.3 Hz, 1H), 7.68 (dd, J = 8.6, 2.4 Hz, 1H), 7.57-7.48 (m, 2H), 7.42 (dd, J = 7.6 Hz, 1H), 7.34 (ddd, J = 7.4, 1.2 Hz, 1H), 7.14 (d, J = 8.0 Hz, 2H), 7.08 (d, J = 7.9 Hz, 2H), 7.05-6.98 (m, 2H), 6.93 (dd, J = 8.0 Hz, 1H), 6.44-6.35 (m, 2H), 6.29 (dd, J = 8.2, 2.1 Hz, 1H), 4.15 (s, 2H), 4.01 (s, 1H), 3.97 (s, 3H), 3.11 (s, 3H), 2.97 (s, 3H), 2.30 (s, 3H). 28 1H NMR (400 MHz, Pyridine-d5) 11.65 (s, 1H), 8.59 (d, J = 2.4 Hz, 1H), 7.77 (dd, J = 1.5 Hz, 1H), 7.68 (dd, J = 8.6, 2.4 Hz, 1H), 7.58 (dd, J = 7.8, 1.3 Hz, 1H), 7.55-7.45 (m, 3H), 7.41 (dd, J = 7.6 Hz, 1H), 7.19-7.03 (m, 6H), 6.99 (t, J = 5.9 Hz, 1H), 6.51 (ddd, J = 7.6, 1.8 Hz, 1H), 4.45 (d, J = 5.8 Hz, 2H), 3.60 (s, 3H), 3.07 (s, 3H), 2.80 (s, 3H).

Production Example (3)

(264) ##STR00075##

(1) 4-methoxy-N,N-dimethyl-3-(N-(3-(phenylamino)phenyl)sulfamoyl)-[1,1-biphenyl]-3-carboxamide

(265) ##STR00076##

(266) To a solution of 3-(N-(3-aminophenyl)sulfamoyl)-4-methoxy-N,N-dimethyl-[1,1-biphenyl]-3-carboxamide hydrochloride (10.0 mg) and phenylboronic acid (5.6 mg) in dichloromethane (2.0 mL) were added TEA (6.4 L) and copper(II) acetate (4.1 mg), and the mixture was stirred at room temperature overnight. After completion of the reaction, the reaction mixture was directly applied to a silica gel column, and purified by column chromatography (eluent: ethyl acetate/hexane=4/1.fwdarw.1/0) to give 4-methoxy-N,N-dimethyl-3-(N-(3-(phenylamino)phenyl)sulfamoyl)-[1,1-biphenyl]-3-carboxamide (8.8 mg).

(267) The compounds described in the following Table 4 were also synthesized similarly from boronic acid having the corresponding R group.

(268) ##STR00077##

(269) TABLE-US-00004 TABLE 4 Ex. No. NHR moiety structure .sup.1H-NMR 29 1H NMR (400 MHz, Chloroform-d) 8.05 (d, J = 2.4 Hz, 1H), 7.72 (dd, J = 8.6, 2.4 Hz, 1H), 7.55 (dd, J = 1.5 Hz, 1H), 7.53 (ddd, J = 7.7, 1.6 Hz, 1H), 7.44 (dd, J = 7.8 Hz, 1H), 7.36 (ddd, J = 7.5, 1.4 Hz, 1H), 7.06 (d, J = 8.7 Hz, 1H), 7.00 (dd, J = 8.0 Hz, 1H), 6.95 (d, J = 9.0 Hz, 2H), 6.85 (s, 1H), 6.79 (d, J = 9.0 Hz, 2H), 6.65 (dd, J = 2.1 Hz, 1H), 6.56 (ddd, J = 8.2, 2.2, 0.8 Hz, 1H), 6.49 (ddd, J = 7.9, 2.0, 0.8 Hz, 1H), 5.48 (s, 1H), 4.01 (s, 3H), 3.77 (s, 3H), 3.13 (s, 3H), 2.99 (s, 3H). 30 1H NMR (400 MHz, Chloroform-d) 7.45 (d, J = 2.4 Hz, 1H), 7.12 (dd, J = 8.6, 2.4 Hz, 1H), 6.96-6.89 (m, 2H), 6.83 (dd, J = 7.6 Hz, 1H), 6.75 (ddd, J = 7.5, 1.3 Hz, 1H), 6.62-6.56 (m, 2H), 6.49-6.43 (m, 2H), 6.37-6.28 (m, 4H), 6.23 (dd, J = 2.1 Hz, 1H), 6.12 (ddd, J = 8.1, 2.2, 0.8 Hz, 1H), 5.98 (ddd, J = 7.9, 2.0, 0.8 Hz, 1H), 5.09 (s, 1H), 3.42 (s, 3H), 2.52 (s, 3H), 2.38 (s, 3H). 31 0 1H NMR (400 MHz, Methanol-d4) 8.02 (d, J = 2.4 Hz, 1H), 7.83 (dd, J = 8.6, 2.4 Hz, 1H), 7.60 (ddd, J = 7.8, 1.8, 1.2 Hz, 1H), 7.55 (dd, J = 1.5 Hz, 1H), 7.51 (dd, J = 7.7 Hz, 1H), 7.38 (ddd, J = 7.5, 1.3 Hz, 1H), 7.23 (d, J = 8.7 Hz, 1H), 7.02 (dd, J = 7.9 Hz, 1H), 6.99 (dd, J = 7.9, 1.5 Hz, 1H), 6.95 (dd, J = 2.1 Hz, 1H), 6.91 (dd, J = 8.1, 1.3 Hz, 1H), 6.80 (ddd, J = 7.8, 1.6 Hz, 1H), 6.70-6.63 (m, 2H), 6.60 (ddd, J = 8.0, 2.0, 0.9 Hz, 1H), 3.97 (s, 3H), 3.80 (s, 3H), 3.10 (s, 3H), 2.99 (s, 3H). 32 1H NMR (400 MHz, Chloroform-d) 8.05 (d, J = 2.4 Hz, 1H), 7.72 (dd, J = 8.6, 2.4 Hz, 1H), 7.54 (dd, J = 1.5 Hz, 1H), 7.51 (ddd, J = 7.8, 1.8, 1.3 Hz, 1H), 7.43 (ddd, J = 7.6, 0.5 Hz, 1H), 7.35 (ddd, J = 7.5, 1.4 Hz, 1H), 7.13-7.03 (m, 3H), 6.93 (s, 1H), 6.87 (dd, J = 2.1 Hz, 1H), 6.74 (ddd, J = 8.1, 2.2, 0.8 Hz, 1H), 6.60 (ddd, J = 8.0, 2.1, 0.9 Hz, 1H), 6.57-6.51 (m, 2H), 6.48 (ddd, J = 8.2, 2.4, 0.9 Hz, 1H), 5.71 (s, 1H), 4.05 (s, 3H), 3.76 (s, 3H), 3.12 (s, 3H), 2.98 (s, 3H). 33 1H NMR (400 MHz, Methanol-d4) 8.03 (d, J = 2.4 Hz, 1H), 7.83 (dd, J = 8.6, 2.5 Hz, 1H), 7.61 (ddd, J = 7.8, 1.9, 1.2 Hz, 1H), 7.55 (dd, J = 1.8 Hz, 1H), 7.51 (dd, J = 7.7 Hz, 1H), 7.38 (ddd, J = 7.6, 1.2 Hz, 1H), 7.23 (d, J = 8.7 Hz, 1H), 7.04 (dd, J = 8.0 Hz, 1H), 6.98 (dd, J = 2.1 Hz, 1H), 6.74 (dd, J = 8.2 Hz, 1H), 6.68 (ddd, J = 8.1, 2.2, 0.9 Hz, 1H), 6.65-6.60 (m, 2H), 6.50 (dd, J = 8.3, 1.4 Hz, 1H), 3.98 (s, 3H), 3.82 (s, 3H), 3.66 (s, 3H), 3.10 (s, 3H), 2.99 (s, 3H). 34 1H NMR (400 MHz, Methanol-d4) 8.05 (d, J = 2.4 Hz, 1H), 7.84 (dd, J = 8.6, 2.4 Hz, 1H), 7.62 (ddd, J = 7.8, 1.9, 1.2 Hz, 1H), 7.56 (dd, J = 1.5 Hz, 1H), 7.51 (dd, J = 7.6 Hz, 1H), 7.38 (ddd, J = 7.6, 1.3 Hz, 1H), 7.25 (d, J = 8.7 Hz, 1H), 7.19 (d, J = 8.8 Hz, 2H), 7.08- 7.05 (m, 2H), 6.91 (d, J = 8.8 Hz, 2H), 6.71 (ddd, J = 8.2, 2.2, 0.9 Hz, 1H), 6.68 (ddd, J = 8.0, 2.0, 0.9 Hz, 1H), 3.99 (s, 3H), 3.10 (s, 3H), 3.05 (s, 6H), 2.98 (s, 3H). 35 1H NMR (400 MHz, Chloroform-d) 8.05 (d, J = 2.3 Hz, 1H), 7.73 (dd, J = 8.6, 2.3 Hz, 1H), 7.57-7.50 (m, 2H), 7.43 (dd, J = 7.6 Hz, 1H), 7.35 (brd, J = 7.6 Hz, 1H), 7.17 (dd, J = 8.2 Hz, 1H), 7.14- 7.06 (m, 2H), 6.95 (s, 1H), 6.88 (dd, J = 2.0 Hz, 1H), 6.84 (dd, J = 8.5, 2.0 Hz, 1H), 6.81-6.76 (m, 2H), 6.73 (brd, J = 8.1 Hz, 1H), 6.66 (brd, J = 7.9 Hz, 1H), 5.83 (s, 1H), 4.06 (s, 3H), 3.13 (s, 3H), 2.99 (s, 3H). 36 1H NMR (400 MHz, Chloroform-d) 8.04 (d, J = 2.4 Hz, 1H), 7.72 (dd, J = 8.6, 2.3 Hz, 1H), 7.57-7.50 (m, 2H), 7.44 (dd, J = 7.8 Hz, 1H), 7.36 (ddd, J = 7.6, 1.4 Hz, 1H), 7.09 (d, J = 8.6 Hz, 1H), 7.02 (dd, J = 8.0 Hz, 1H), 6.90 (brs, 1H), 6.70-6.64 (m, 2H), 6.58 (ddd, J = 8.2, 2.2, 0.8 Hz, 1H), 6.56- 6.51 (m, 2H), 6.43 (dd, J = 8.2, 2.2 Hz, 1H), 5.92 (s, 2H), 5.51 (brs, 1H), 4.03 (s, 3H), 3.13 (s, 3H), 2.99 (s, 3H).

Production Example (4)

(270) ##STR00086##

(1) 4-methoxy-N,N-dimethyl-3-(N-(3-(3-phenylureido)phenyl)sulfamoyl)-[1,1-biphenyl]-3-carboxamide

(271) ##STR00087##

(272) Under an argon atmosphere, to a suspension of 3-(N-(3-aminophenyl)sulfamoyl)-4-methoxy-N,N-dimethyl-[1,1-biphenyl]-3-carboxamide hydrochloride (12.0 mg) in dichloromethane (4.0 mL) were added TEA (10.0 L) and phenyl isocyanate (10.0 L), and the mixture was stirred at room temperature for 20 hr. The reaction mixture was diluted with 20% methanol-containing chloroform, and extracted with saturated aqueous ammonium chloride solution. The organic layer was washed with saturated brine, dried over sodium sulfate and filtered, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by preparative thin layer chromatography (eluent: chloroform/methanol=10/1) to give 4-methoxy-N,N-dimethyl-3-(N-(3-(3-phenylureido)phenyl)sulfamoyl)-[1,1-biphenyl]-3-carboxamide (3.9 mg).

(273) The compounds described in the following Tables 5-8 were also synthesized similarly from isocyanate having the corresponding R group, isocyanate developed from carboxylic acid having R group or chloroformic acid ester.

(274) ##STR00088##

(275) TABLE-US-00005 TABLE 5 Ex. No. NHCONHR moiety structure .sup.1H-NMR 37 1H NMR (400 MHz, Methanol-d) 8.06 (d, J = 2.0 Hz, 1H), 7.77 (dd, J = 8.8, 2.0 Hz, 1H), 7.64 (m, 1H), 7.55 (t, J = 1.6 Hz, 1H), 7.44 (m, 2H), 7.36 (m, 3H), 7.25 (m, 2H), 7.19 (d, J = 8.8 Hz, 1H), 7.06 (t, J = 8.0 Hz, 1H), 6.99 (m, 2H), 6.78 (m, 1H), 4.00 (s, 3H), 3.07 (s, 3H), 2.99 (s, 3H). 38 0 1H NMR (400 MHz, Methanol-d) 8.06 (d, J = 2.4 Hz, 1H), 7.79 (dd, J = 8.4, 2.4 Hz, 1H), 7.66 (m, 1H), 7.55 (t, J = 2.0 Hz, 1H), 7.45 (t, J = 8.0 Hz, 1H), 7.42 (t, J = 2.4 Hz, 1H), 7.35 (m, 1H), 7.20 (m, 2H), 7.16-7.13 (m, 2H), 7.11-7.05 (m, 1H) 7.00-6.98 (m, 1H), 6.83 (d, J = 7.6 Hz, 1H), 6.79-6.77 (m, 1H), 4.01 (s, 3H), 3.08 (s, 3H), 2.98 (s, 3H), 2.29 (s, 3H). 39 1H NMR (400 MHz, DMSO-d6) 10.06 (s, 1H), 8.54 (s, 1H), 8.17 (s, 1H), 8.03 (d, J = 2.4 Hz, 1H), 7.89 (dd, J = 8.8, 2.4 Hz, 1H), 7.70 (d, J = 8.4 Hz, 1H), 7.57 (s, 1H), 7.45 (t, J = 7.6 Hz, 1H), 7.35-7.34 (m, 2H), 7.26 (d, J = 8.8 Hz, 1H), 7.19 (d, J = 9.2 Hz, 2H), 7.05-6.99 (m, 2H), 6.67 (t, J = 8.4 Hz, 3H), 3.94 (s, 3H), 2.97 (s, 3H), 2.88 (s, 3H), 2.81 (s, 6H). 40 1H NMR (400 MHz, DMSO-d6) 10.05 (s, 1H), 8.58 (s, 1H), 8.34 (s, 1H), 7.99 (d, J = 2.4 Hz, 1H), 7.89 (dd, J = 8.8, 2.4 Hz, 1H), 7.68 (d, J = 8.4 Hz, 1H), 7.56 (s, 1H), 7.45 (t, J = 7.6 Hz, 1H), 7.35-7.32 (m, 2H), 7.26 (d, J = 8.4 Hz, 1H), 7.07- 7.02 (m, 3H), 6.81 (m, 1H), 6.73-6.69 (m, 1H), 6.68 (d, J = 8.0 Hz, 1H), 6.34 (dd, J = 8.0, 2.0 Hz, 1H), 3.94 (s, 3H), 2.97 (s, 3H), 2.88 (s, 3H), 2.85 (s, 6H). 41 1H NMR (400 MHz, Methanol-d) 8.08 (d, J = 3.6 Hz, 1H), 8.02 (dd, J = 8.0, 2.0 Hz, 1H), 7.79 (dd, J = 8.8, 2.4 Hz, 1H), 7.67 (d, J = 8.0 Hz, 1H), 7.57 (s, 1H), 7.50 (t, J = 2.0 Hz, 1H), 7.44 (t, J = 8.0 Hz, 1H), 7.35 (d, J = 7.6 Hz, 1H), 7.22-7.17 (m, 2H), 7.08-6.95 (m, 4H), 6.80-6.8 (m, 1H), 4.03 (s, 3H), 3.08 (s, 3H), 2.98 (s, 3H), 2.62 (s, 6H). 42 1H NMR (400 MHz, Pyridine-d5) 12.03 (brs, 1H), 9.51 (s, 1H), 9.40 (s, 1H), 8.66 (d, J = 2.0 Hz, 1H), 8.46 (s, 1H), 7.80-7.62 (m, 5H), 7.50-7.39 (m, 5H), 7.22-7.17 (m, 2H), 7.07 (d, J = 8.8 Hz, 1H), 3.71 (s, 3H), 3.05 (s, 3H), 2.79 (s, 3H). 43 1H NMR (400 MHz, DMSO-d6) 12.02 (s, 1H), 10.54 (s, 1H), 8.66-8.63 (m, 2H), 8.46 (s, 1H), 8.03 (s, 1H), 7.79 (s, 1H), 7.68 (dd, J = 8.8, 2.0 Hz, 1H), 7.63 (d, J = 8.0 Hz, 1H), 7.51-7.46 (m, 3H), 7.41 (t, J = 8.0 Hz, 1H), 7.33 (m, 1H), 7.21 (s, 1H), 7.19 (d, J = 5.6 Hz, 1H), 7.09 (d, J = 8.8 Hz, 1H), 6.87 (m, 1H), 3.71 (s, 3H), 3.05 (s, 3H), 2.79 (s, 3H). 44 1H NMR (400 MHz, DMSO-d6) 10.07 (s, 1H), 8.67 (s, 1H), 8.54 (s, 1H), 8.00 (d, J = 2.4 Hz, 1H), 7.89 (dd, J = 8.8, 2.4 Hz, 1H), 7.69 (d, J = 8.0 Hz, 1H), 7.57 (s, 1H), 7.46 (t, J = 7.6 Hz, 1H), 7.35-7.31 (m, 2H), 7.26 (d, J = 8.8 Hz, 1H), 7.15 (t, J = 8.4 Hz, 1H), 7.11 (s, 1H), 7.08- 7.02 (m, 2H), 6.89 (d, J = 8.4 Hz, 1H), 6.73 (d, J = 6.8 Hz, 1H), 6.54 (dd, J = 8.4, 2.4 Hz, 1H), 3.94 (s, 3H), 3.71 (s, 3H), 2.97 (s, 3H), 2.89 (s, 3H). 45 1H NMR (400 MHz, Chloroform-d) 8.06 (s, 1H), 7.99 (s, 1H), 7.85 (s, 1H), 7.72 (brs, 1H), 7.59 (d, J = 7.6 Hz, 1H), 7.55- 7.50 (m, 3H), 7.40 (d, J = 6.4 Hz, 1H), 7.35-7.17 (m, 5H), 6.96 (d, J = 8.4 Hz, 1H), 6.87 (t, J = 8.0 Hz, 1H), 6.81 (d, J = 7.6 Hz, 1H), 6.67 (d, J = 7.6 Hz, 1H), 3.98 (s, 3H), 3.82 (s, 3H), 3.16 (s, 3H), 3.01 (s, 3H). 46 1H NMR (400 MHz, Chloroform-d) 9.77 (s, 1H), 8.66 (s, 1H), 8.46 (d, J = 8.8 Hz, 1H), 8.08 (dd, J = 8.0, 1.2 Hz, 1H), 8.00 (d, J = 2.4 Hz, 1H), 7.54-7.41 (m, 4H), 7.32-7.26 (m, 4H), 7.09 (d, J = 8.4 Hz, 1H), 7.03-6.95 (m, 3H), 6.78 (d, J = 8.0 Hz, 1H), 4.01 (s, 3H), 3.15 (s, 3H), 3.00 (s, 3H).

(276) TABLE-US-00006 TABLE 6 Ex. No. NHCONHR moiety structure .sup.1H-NMR 47 1H NMR (400 MHz, DMSO-d6) 10.13 (s, 1H), 9.53 (s, 1H), 9.15 (s, 1H), 8.69 (s, 2H), 8.39 (s, 1H), 8.00 (s, 1H), 7.90 (d, J = 8.4 Hz, 1H), 7.67 (d, J = 7.6 Hz, 1H), 7.59 (s, 1H), 7.44 (t, J = 7.2 Hz, 1H), 7.38-7.32 (m, 2H), 7.27 (d, J = 8.8 Hz, 1H), 7.14-7.08 (m, 2H), 6.78 (d, J = 6.8 Hz, 1H), 3.94 (s, 3H), 2.97 (s, 3H), 2.90 (s, 3H). 48 00 1H NMR (400 MHz, Methanol-d) 8.06 (d, J = 2.4 Hz, 1H), 8.02 (s, 1H), 7.77 (dd, J = 8.8, 2.4 Hz, 1H), 7.67-7.63 (m, 3H), 7.55 (s, 1H), 7.46-7.45 (m, 1H), 7.43 (d, J = 7.6 Hz, 1H), 7.37-7.32 (m, 2H), 7.19 (d, J = 8.8 Hz, 1H), 7.07 (t, J = 8.0 Hz, 1H), 6.98 (d, J = 8.8 Hz, 1H), 6.81-6.78 (m, 1H), 4.01 (s, 3H), 3.07 (s, 3H), 2.97 (s, 3H). 49 01 1H NMR (400 MHz, Chloroform-d) 8.22 (s, 1H), 8.03 (s, 1H), 8.00 (d, J = 2.0 Hz, 1H), 7.61 (dd, J = 8.8, 2.4 Hz, 1H), 7.52- 7.49 (m, 2H), 7.37-7.23 (m, 6H), 7.12 (t, J = 8.0 Hz, 1H), 7.01-6.96 (m, 3H), 6.92 (d, J = 8.0 Hz, 1H), 6.71 (m, 1H), 4.01 (s, 3H), 3.12 (s, 3H), 3.10 (s, 3H), 2.99 (s, 3H), 2.95 (s, 3H). 50 02 1H NMR (400 MHz, Methanol-d) 8.07 (d, J = 2.0 Hz, 1H), 7.79 (d, J = 8.8 Hz, 1H), 7.74 (dd, J = 1.6 Hz, 1H), 7.66 (d, J = 8.0 Hz, 1H), 7.56 (s, 1H), 7.48-7.45 (m, 2H), 7.35 (d, J = 8.0 Hz, 1H), 7.27 (dt, J = 8.0, 2.0 Hz, 1H), 7.21 (d, J = 8.8 Hz, 1H), 7.19-7.13 (m, 2H), 7.08 (t, J = 8.0 Hz, 1H), 6.98 (d, J = 9.2 Hz, 1H), 6.80 (m, 1H), 4.02 (s, 3H), 3.09 (s, 3H), 2.99 (s, 3H). 51 03 1H NMR (400 MHz, Chloroform-d) 8.49 (brs, 1H), 8.07 (d, J = 2.4 Hz, 1H), 7.64 (s, 1H), 7.60 (dd, J = 8.8, 2.4 Hz, 1H), 7.54 (s, 1H), 7.48 (d, J = 8.0 Hz, 1H), 7.41 (d, J = 8.4 Hz, 1H), 7.37-7.26 (m, 4H), 7.15-7.03 (m, 3H), 6.99-6.93 (m, 2H), 6.87 (d, J = 8.0 Hz, 1H), 6.62 (d, J = 7.6 Hz, 1H), 3.98 (s, 3H), 3.13 (s, 3H), 3.00 (s, 3H), 2.16 (s, 3H). 52 04 1H NMR (400 MHz, Pyridine-d5) 12.02 (brs, 1H), 10.22 (s, 1H), 8.82 (d, J = 6.8 Hz, 1H), 8.68 (d, J = 1.6 Hz, 1H), 8.50 (s, 1H), 8.24 (s, 1H), 7.78 (s, 1H), 7.68- 7.64 (m, 2H), 7.51-7.40 (m, 3H), 7.20-7.16 (m, 2H), 7.09-7.07 (m, 2H), 6.99 (t, J= 7.2 Hz, 1H), 6.82 (d, J = 7.2 Hz, 1H), 3.72 (s, 3H), 3.34 (s, 3H), 3.05 (s, 3H), 2.78 (s, 3H). 53 05 1H NMR (400 MHz, Pyridine-d5) 12.02 (brs, 1H), 9.39 (s, 1H), 9.07 (s, 1H), 8.67 (d, J = 2.4 Hz, 1H), 8.52 (s, 1H), 7.80 (s, 1H), 7.71 (d, J = 9.2 Hz, 2H), 7.68-7.63 (m, 2H), 7.50 (d, J = 8.0 Hz, 1H), 7.46-7.40 (m, 2H), 7.18-7.15 (m, 2H), 7.07 (d, J = 8.8 Hz, 1H), 6.98 (d, J = 6.8 Hz, 2H), 3.71 (s, 3H), 3.66 (s, 3H), 3.05 (s, 3H), 2.79 (s, 3H). 54 06 1H NMR (400 MHz, DMSO-d6) 10.06 (s, 1H), 8.64 (s, 1H), 8.47 (s, 1H), 7.98 (s, 1H), 7.89 (d, J = 8.8 Hz, 1H), 7.67 (d, J = 7.6 Hz, 1H), 7.57 (s, 1H), 7.44 (t, J = 7.6 Hz, 1H), 7.33 (d, J = 7.6 Hz, 1H), 7.30- 7.26 (m, 2H), 7.09-7.03 (m, 2H), 6.74-6.71 (m, 3H), 3.94 (s, 3H), 3.71 (s, 6H), 3.59 (s, 3H), 2.98 (s, 3H), 2.89 (s, 3H). 55 07 1H NMR (400 MHz, DMSO-d6) 8.15 (brs, 1H), 8.01 (d, J = 2.4 Hz, 1H), 7.66-7.60 (m, 2H), 7.43 (t, J = 8.0 Hz, 1H), 7.43 (s, 1H), 7.28 (d, J = 8.0 Hz, 1H), 7.06 (d, J = 8.8 Hz, 1H), 7.01 (d, J = 8.4 Hz, 2H), 6.84-6.73 (m, 3H), 6.46 (d, J = 8.4 Hz, 2H), 6.39 (d, J = 1.6 Hz, 1H), 4.70 (s, 2H), 4.13 (brs, 1H), 3.78 (s, 3H), 2.97 (s, 3H), 2.86 (s, 3H). 56 08 1H NMR (400 MHz, DMSO-d6) 10.08 (s, 1H), 8.61 (s, 1H), 8.39 (s, 1H), 8.01 (d, J = 2.8 Hz, 1H), 7.89 (dd, J = 8.8, 2.4 Hz, 1H), 7.70 (d, J = 8.4 Hz, 1H), 7.57 (s, 1H), 7.45 (t, J = 7.6 Hz, 1H), 7.36-7.33 (m, 2H), 7.27-7.25 (m, 3H), 7.07-7.00 (m, 4H), 7.70 (dt, J = 7.2, 1.6 Hz, 1H), 3.94 (s, 3H), 2.97 (s, 3H), 2.88 (s, 3H), 2.23 (s, 3H). 57 09 1H NMR (400 MHz, DMSO-d6) 10.12 (s, 1H), 9.05 (s, 1H), 8.88 (s, 1H), 8.49 (t, J = 2.0 Hz, 1H), 8.01 (d, J = 2.4 Hz, 1H), 7.90 (dd, J = 8.8, 2.0 Hz, 1H), 7.80 (dd, J = 8.0, 2.0 Hz, 1H), 7.69-7.66 (m, 2H), 7.58 (s, 1H), 7.54 (t, J = 8.0 Hz, 1H), 7.44 (t, J = 8.0 Hz, 1H), 7.37 (s, 1H), 7.33 (d, J = 7.6 Hz, 1H), 7.26 (d, J = 8.8 Hz, 1H), 7.10-7.07 (m, 2H), 6.77-6.74 (m, 1H), 3.94 (s, 3H), 2.97 (s, 3H), 2.88 (s, 3H).

(277) TABLE-US-00007 TABLE 7 Ex. NHCONHR moiety No. structure .sup.1H-NMR 58 0 1H NMR (400 MHz, DMSO-d6) 11.45 (s, 1H), 10.07 (brs, 1H), 9.89 (s, 1H), 8.82 (brs, 1H), 8.72 (brs, 1H), 8.02 (s, 1H), 7.89 (dd, J = 8.0, 2.0 Hz, 1H), 7.70 (d, J = 8.0 Hz, 1H), 7.57 (s, 1H), 7.46 (t, J = 7.6 Hz, 1H), 7.41-7.34 (m, 6H), 7.26 (d, J = 8.8 Hz, 1H), 7.05 (t, J = 8.0 Hz, 1H), 6.99 (d, J = 8.0 Hz, 1H), 6.71 (d, J = 8.0 Hz, 1H), 3.94 (s, 3H), 2.97 (s, 3H), 2.88 (s, 3H), 1.51 (s, 9H), 1.39 (s, 9H). 59 1H NMR (400 MHz, Methanol-d) 8.08 (d, J = 2.4 Hz, 1H), 7.80 (dd, J = 8.4, 2.0 Hz, 1H), 7.67 (d, J = 8.0 Hz, 1H), 7.58 (s, 1H), 7.48 (t, J = 8.0 Hz, 1H), 7.46- 7.42 (m, 3H), 7.36 (d, J = 7.2 Hz, 1H), 7.22 (d, J = 8.8 Hz, 1H), 7.17 (d, J = 8.8 Hz, 2H), 7.08 (t, J = 8.0 Hz, 1H), 6.99-6.96 (m, 1H), 6.79-6.77 (m, 1H), 4.02 (s, 3H), 3.09 (s, 3H), 3.00 (s, 3H), 1.50 (s, 9H). 60 1H NMR (400 MHz, Methanol-d) 8.08 (d, J = 2.4 Hz, 1H), 7.81 (dd, J = 8.4, 2.8 Hz, 1H), 7.68 (dt, J = 7.6, 2.0 Hz, 1H), 7.58 (t, J = 1.6 Hz, 1H), 7.51-7.47 (m, 4H), 7.36 (dt, J = 8.0, 1.6 Hz, 1H), 7.22 (d, J = 8.8 Hz, 1H), 7.18 (d, J = 9.2 Hz, 2H), 7.09 (t, J = 8.4 Hz, 1H), 7.00-6.98 (m, 1H), 6.78-6.75 (m, 1H), 4.02 (s, 3H), 3.09 (s, 3H), 3.00 (s, 3H). 61 1H NMR (400 MHz, DMSO-d6) 10.14 (s, 1H), 9.36 (s, 1H), 8.99 (s, 1H), 8.16 (d, J = 9.2 Hz, 2H), 8.03 (d, J = 2.4 Hz, 1H), 7.90 (dd, J = 8.8, 2.4 Hz, 1H), 7.70 (d, J = 7.6 Hz, 1H), 7.61 (d, J = 9.2 Hz, 2H), 7.59 (s, 1H), 7.46 (t, J = 8.0 Hz, 1H), 7.40 (s, 1H), 7.34 (d, J = 8.0 Hz, 1H), 7.26 (d, J = 8.8 Hz, 1H), 7.09 (t, J = 8.0 Hz, 1H), 7.03 (d, J = 8.0 Hz, 1H), 6.76 (d, J = 8.4 Hz, 1H), 3.94 (s, 3H), 2.97 (s, 3H), 2.88 (s, 3H). 62 1H NMR (400 MHz, DMSO-d6) 10.03 (brs, 1H), 9.31 (s, 1H), 8.55 (s, 1H), 8.51 (s, 1H), 8.00 (d, J = 2.0 Hz, 1H), 7.89 (dd, J = 8.8, 2.4 Hz, 1H), 7.69 (d, J = 7.6 Hz, 1H), 7.57 (s, 1H), 7.51 (s, 1H), 7.45 (t, J = 8.0 Hz, 1H), 7.34-7.32 (m, 2H), 7.26 (d, J = 8.8 Hz, 1H), 7.12-6.99 (m, 5H), 6.72 (d, J = 7.2 Hz, 1H), 3.94 (s, 3H), 2.97 (s, 3H), 2.88 (s, 3H), 1.46 (s, 9H). 63 1H NMR (400 MHz, DMSO-d6) 10.01 (brs, 1H), 8.31 (brs, 2H), 8.01 (d, J = 2.0 Hz, 1H), 7.74 (brs, 1H), 7.65 (d, J = 7.2 Hz, 1H), 7.50-7.42 (m, 2H), 7.30 (d, J = 7.6 Hz, 1H), 7.14 (brs, 1H), 6.91 (brs, 1H), 6.85 (t, J = 8.0 Hz, 2H), 6.72 (s, 1H), 6.55-6.49 (m, 2H), 6.14 (d, J = 8.0 Hz, 1H), 5.00 (s, 2H), 3.85 (s, 3H), 2.97 (s, 3H), 2.87 (s, 3H). 64 1H NMR (400 MHz, DMSO-d6) 9.97 (brs, 1H), 8.70 (s, 1H), 8.61 (s, 1H), 8.00 (d, J = 2.4 Hz, 1H), 7.89 (d, J = 8.8 Hz, 1H), 7.69 (d, J = 7.6 Hz, 1H), 7.57 (s, 1H), 7.49 (s, 1H), 7.44 (t, J = 7.6 Hz, 1H), 7.34-7.32 (m, 2H), 7.28-7.20 (m, 4H), 7.05 (m, 2H), 6.73 (m, 1H), 3.94 (s, 3H), 2.97 (s, 3H), 2.88 (s, 3H), 1.50 (brs, 9H), 1.39 (brs, 9H). 65 1H NMR (400 MHz, DMSO-d6) 8.33 (brs, 1H), 8.28 (brs, 1H), 8.00 (d, J = 2.4 Hz, 1H), 7.60 (d, J = 7.2 Hz, 2H), 7.46- 7.42 (m, 2H), 7.28 (d, J = 7.6 Hz, 1H), 7.07-6.77 (m, 6H), 6.42 (brs, 1H), 6.34 (brs, 1H), 5.08 (brs, 2H), 4.09 (brs, 3H), 3.78 (s, 3H), 2.97 (s, 3H), 2.86 (s, 3H). 66 1H NMR (400 MHz, DMSO-d6) 10.02 (s, 1H), 8.55 (s, 1H), 7.99 (d, J = 2.4 Hz, 1H), 7.89 (dd, J = 8.4, 2.4 Hz, 1H), 7.69 (d, J = 7.6 Hz, 1H), 7.60 (s, 1H), 7.46 (t, J = 8.0 Hz, 1H), 7.34 (d, J = 7.2 Hz, 1H), 7.33-7.20 (m, 7H), 7.02- 6.99 (m, 2H), 6.66-6.63 (m, 1H), 6.46 (t, J = 6.4 Hz, 1H), 4.24 (d, J = 6.4 Hz, 2H), 3.92 (s, 3H), 2.97 (s, 3H), 2.89 (s, 3H). 67 1H NMR (400 MHz, DMSO-d6) 10.09 (s, 1H), 9.44 (s, 1H), 8.74 (s, 1H), 8.01 (d, J = 2.4 Hz, 1H), 7.89 (dd, J = 8.4, 2.0 Hz, 1H), 7.68 (d, J = 8.4 Hz, 1H), 7.58 (s, 1H), 7.46 (t, J = 7.6 Hz, 1H), 7.37-7.33 (m, 2H), 7.26 (d, J = 8.4 Hz, 1H), 7.06 (t, J = 8.0 Hz, 1H), 7.01 (d, J = 8.4 Hz, 1H), 6.85 (dd, J = 5.6, 1.2 Hz, 1H), 6.80-6.77 (m, 1H), 6.73 (d, J = 8.0 Hz, 1H), 6.51 (dd, J = 3.6, 1.2 Hz, 1H), 3.94 (s, 3H), 2.98 (s, 3H), 2.89 (s, 3H). 68 0 1H NMR (400 MHz, DMSO-d6) 10.18 (s, 1H), 10.12 (s, 1H), 9.25 (s, 1H), 8.18 (d, J = 3.2 Hz, 1H), 8.02 (d, J = 2.4 Hz, 1H), 7.90 (dd, J = 8.8, 2.4 Hz, 1H), 7.74-7.68 (m, 2H), 7.59 (s, 1H), 7.50- 7.43 (m, 3H), 7.35 (d, J = 7.2 Hz, 1H), 7.26 (d, J = 8.8 Hz, 1H), 7.09 (t, J = 8.0 Hz, 1H), 7.04 (d, J = 8.0 Hz, 1H), 6.97 (dd, J = 7.2, 5.2 Hz, 1H), 6.78 (d, J = 8.0 Hz, 1H), 3.94 (s, 3H), 2.98 (s, 3H), 2.88 (s, 3H).

(278) TABLE-US-00008 TABLE 8 Ex. NHCONHR moiety No. structure .sup.1H-NMR 69 1H NMR (400 MHz, DMSO-d6) 10.11 (s, 1H), 8.82 (s, 1H), 8.68 (s, 1H), 8.55 (d, J = 2.4 Hz, 1H), 8.17 (dd, J = 8.4, 1.6 Hz, 1H), 8.02 (d, J = 6.4 Hz, 1H), 7.89 (dd, J = 8.8, 2.8 Hz, 1H), 7.88-7.85 (m, 1H), 7.70 (d, J = 8.0 Hz, 1H), 7.58 (s, 1H), 7.46 (t, J = 7.6 Hz, 1H), 7.38 (s, 1H), 7.34 (d, J = 7.6 Hz, 1H), 7.30-7.25 (m, 2H), 7.07 (t, J = 8.0 Hz, 1H), 7.02 (d, J = 8.8 Hz, 1H), 6.73 (d, J = 8.0 Hz, 1H), 3.94 (s, 3H), 2.97 (s, 3H), 2.88 (s, 3H). 70 1H NMR (400 MHz, DMSO-d6) 8.95 (s, 1H), 8.88 (s, 1H), 8.33-8.31 (m, 3H), 8.03 (d, J = 2.4 Hz, 1H), 7.90 (dd, J = 8.4, 2.0 Hz, 1H), 7.70 (d, J = 8.0 Hz, 1H), 7.58 (s, 1H), 7.46 (t, J = 8.0 Hz, 1H), 7.40-7.34 (m, 4H), 7.26 (d, J = 9.2 Hz, 1H), 7.08 (t, J = 8.0 Hz, 1H). 6.99 (d, J = 8.4 Hz, 1H), 6.74 (d, J = 7.6 Hz, 1H), 3.94 (s, 3H), 2.97 (s, 3H), 2.88 (s, 3H). 71 1H NMR (400 MHz, DMSO-d6) 10.11 (s, 1H), 9.03 (brs, 1H), 8.82 (brs, 1H), 8.14 (d, J = 0.8 Hz, 1H), 8.01 (d, J = 2.4 Hz, 1H), 7.90 (dd, J = 8.8, 2.4 Hz, 1H), 7.77 (d, J = 9.6 Hz, 1H), 7.68 (d, J = 8.4 Hz, 1H), 7.60 (s, 1H), 7.46 (t, J = 8.0 Hz, 1H), 7.37 (s, 1H), 7.35 (d, J = 7.6 Hz, 1H), 7.26 (d, J = 7.6 Hz, 1H), 7.12 (brs, 1H), 7.06 (t, J = 8.0 Hz, 1H), 7.01 (d, J = 8.0 Hz, 1H), 6.72 (d, J = 7.6 Hz, 1H), 3.94 (s, 3H), 3.14 (s, 6H), 2.99 (s, 3H), 2.90 (s, 3H). 72 1H NMR (400 MHz, Methanol-d) 8.07 (d, J = 2.4 Hz, 1H), 7.79 (dd, J = 8.8, 2.8 Hz, 1H), 7.66 (dt, J = 8.0, 1.6 Hz, 1H), 7.56 (t, J = 1.6 Hz, 1H), 7.46 (t, J = 8.0 Hz, 1H), 7.43 (t, J = 1.6 Hz, 1H), 7.29 (dt, J = 8.0, 1.6 Hz, 1H), 7.31-7.25 (m, 4H), 7.20 (d, J = 8.8 Hz, 1H), 7.06 (t, J = 8.0 Hz, 1H), 6.97-6.94 (m, 1H), 6.79-6.76 (m, 1H), 4.01 (s, 3H), 3.08 (s, 3H), 2.98 (s, 3H), 1.51 (s, 9H). 73 1H NMR (400 MHz, DMSO-d6) 10.09 (s, 1H), 9.72 (s, 1H), 8.01 (d, J = 2.8 Hz, 1H), 7.89 (dd, J = 8.8, 2.4 Hz, 1H), 7.69 (d, J = 8.0 Hz, 1H), 7.62 (s, 1H), 7.50-7.47 (m, 2H), 7.38-7.30 (m, 6H), 7.25 (d, J = 8.8 Hz, 1H), 7.05 (t, J = 8.0 Hz, 1H), 6.97 (d, J = 8.8 Hz, 1H), 6.73 (d, J = 8.4 Hz, 1H), 5.07 (s, 2H), 3.92 (s, 3H), 2.96 (s, 3H), 2.89 (s, 3H). 74 1H NMR (400 MHz, DMSO-d6) 10.05 (s, 1H), 9.30 (s, 1H), 8.00 (d, J = 2.4 Hz, 1H), 7.90 (dd, J = 8.4, 2.4 Hz, 1H), 7.69 (d, J = 8.4 Hz, 1H), 7.59 (s, 1H), 7.49 (t, J = 8.0 Hz, 1H), 7.43 (s, 1H), 7.35 (d, J = 8.4 Hz, 1H), 7.02 (t, J = 8.0 Hz, 1H), 6.66 (d J = 8.0 Hz, 1H), 3.92 (s, 3H), 2.99 (s, 3H), 2.91 (s, 3H), 1.39 (s, 9H).

Production Example (5)

(279) ##STR00127##

(1) 4-methoxy-N,N-dimethyl-3-(N-(3-(3-phenylthioureido)phenyl)sulfamoyl)-[1,1-biphenyl]-3-carboxamide

(280) ##STR00128##

(281) Under an argon atmosphere, to a solution of 3-(N-(3-aminophenyl)sulfamoyl)-4-methoxy-N,N-dimethyl-[1,1-biphenyl]-3-carboxamide hydrochloride (16.5 mg) in anhydrous benzene (3.0 mL) were added TEA (30.0 L) and phenyl isothiocyanate (30.0 mg), and the mixture was stirred under reflux at 110 C. for 12 hr. The reaction mixture was diluted with 20% methanol-containing chloroform, and extracted with saturated aqueous ammonium chloride solution. The organic layer was washed with saturated aqueous sodium hydrogen carbonate solution and saturated brine, dried over sodium sulfate and filtered, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by preparative thin layer chromatography (eluent: chloroform/methanol=10/1) to give 4-methoxy-N,N-dimethyl-3-(N-(3-(3-phenylthioureido)phenyl)sulfamoyl)-[1,1-biphenyl]-3-carboxamide (7.1 mg).

(282) The compounds described in the following Table 9 were also synthesized similarly from isothiocyanate having the corresponding R group.

(283) ##STR00129##

(284) TABLE-US-00009 TABLE 9 NHCSNHR moiety Ex. No. structure .sup.1H-NMR 75 0 1H NMR (400 MHz, Chloroform-d) 8.05 (brs, 1H), 8.00 (d, J = 2.0 Hz, 1H), 7.88 (brs, 1H), 7.65 (d, J = 8.8 Hz, 1H), 7.52 (s, 1H), 7.49 (d, J = 8.0 Hz, 1H), 7.41 (d, J = 7.2 Hz, 1H), 7.38-7.25 (m, 8H), 7.15 (t, J = 8.0 Hz, 1H), 7.03 (d, J = 8.8 Hz, 1H), 6.98 (dd, J = 8.0, 2.0 Hz, 2H), 4.06 (s, 3H), 3.12 (s, 3H), 3.00 (s, 3H). 76 1H NMR (400 MHz, Chloroform-d) 8.01- 7.97 (m, 2H), 7.83 (brs, 1H), 7.66 (d, J = 8.4 Hz, 1H), 7.52 (s, 1H), 7.50 (d, J = 7.6 Hz, 1H), 7.42-7.39 (m, 2H), 7.39- 7.25 (m, 3H), 7.17-6.98 (m, 7H), 4.07 (s, 3H), 3.13 (s, 3H), 3.00 (s, 3H), 2.34 (s, 3H).

(2) 4-methoxy-N,N-dimethyl-3-(N-(3-(3-phenylguanidino)phenyl)sulfamoyl)-[1,1-biphenyl]-3-carboxamide

(285) ##STR00132##

(286) Under an argon atmosphere, to a solution of 4-methoxy-N,N-dimethyl-3-(N-(3-(3-phenylthioureido)phenyl)sulfamoyl)-[1,1-biphenyl]-3-carboxamide (10.9 mg) in acetonitrile (2.0 mL) were added 30% aqueous ammonia solution (1.0 mL) and IBX (37.9 mg), and the mixture was stirred at room temperature for 4 hr. The reaction mixture was diluted with 20% methanol-containing chloroform, and extracted with saturated aqueous sodium hydrogen carbonate solution. The organic layer was washed with saturated brine, dried over sodium sulfate and filtered, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by preparative thin layer chromatography (eluent: chloroform/ammonia-saturated methanol=87/13) to give 4-methoxy-N,N-dimethyl-3-(N-(3-(3-phenylguanidino)phenyl)sulfamoyl)-[1,1-biphenyl]-3-carboxamide (5.1 mg).

(287) The compounds described in the following Table 10 were also synthesized similarly from thiourea derivative having the corresponding R group.

(288) ##STR00133##

(289) TABLE-US-00010 TABLE 10 NHCNHNHR Ex. No. moiety structure .sup.1H-NMR 77 1H NMR (400 MHz, Methanol-d) 8.06 (d, J = 2.4 Hz, 1H), 7.80 (dd, J = 8.4, 2.0 Hz, 1H), 7.63 (m, 1H), 7.57 (t, J = 1.6 Hz, 1H), 7.50 (t, J = 8.0 Hz, 1H), 7.37 (m, 1H), 7.29 (t, J = 7.6 Hz, 1H), 7.21 (d, J = 8.4 Hz, 1H), 7.17-7.13 (m, 3H), 7.11-7.06 (m, 2H), 6.87 (m, 1H), 6.81 (d, J = 8.0 Hz, 1H), 3.98 (s, 3H), 3.10 (s, 3H), 3.00 (s, 3H). 78 1H NMR (400 MHz, Chloroform-d) 8.02 (d, J = 2.4 Hz, 1H), 7.66 (dd, J = 8.8, 2.4 Hz, 1H), 7.54 (s, 1H), 7.51 (d, J = 8.0 Hz, 1H), 7.40 (t, J = 7.6 Hz, 1H), 7.30 (d, J = 8.0 Hz, 1H), 7.18 (t, J = 7.6 Hz, 1H), 7.12 (t, J = 7.6 Hz, 1H), 7.05-6.98 (m, 3H), 6.95 (s, 1H), 6.91 (d, J = 8.0 Hz, 1H), 6.81 (d, J = 8.0 Hz, 1H), 6.76 (d, J = 8.0 Hz, 1H), 5.32- 5.12 (brs, 1H), 4.03 (s, 3H), 3.09 (s, 3H), 2.99 (s, 3H), 2.81-2.08 (brs, 2H), 2.30 (s, 3H).

Production Example (6)

(290) ##STR00136##

(1) 4-methoxy-3-(N-(3-((2-methoxy-3,4-dioxocyclobut-1-en-1-yl)amino)phenyl)sulfamoyl)-N,N-dimethyl-[1,1-biphenyl]-3-carboxamide

(291) ##STR00137##

(292) Under an argon atmosphere, to a suspension of 3-(N-(3-aminophenyl)sulfamoyl)-4-methoxy-N,N-dimethyl-[1,1-biphenyl]-3-carboxamide hydrochloride (149.0 mg) in methanol (5.0 mL) were added TEA (88.0 L) and 3,4-dimethoxy-3-cyclobutene-1,2-dione (48.4 mg), and the mixture was stirred at room temperature for 15 hr. The reaction mixture was concentrated under reduced pressure, the obtained residue was crudely purified by silica gel column chromatography (eluent: chloroform/ethyl acetate=4/1), and the crude product was recrystallized from chloroform to give 4-methoxy-3-(N-(3-((2-methoxy-3,4-dioxocyclobut-1-en-1-yl)amino)phenyl)sulfamoyl)-N,N-dimethyl-[1,1-biphenyl]-3-carboxamide (150.2 mg) as colorless needle crystals.

(2) 3-(N-(3-((3,4-dioxo-2-(m-tolylamino)cyclobut-1-en-1-yl)amino)phenyl)sulfamoyl)-4-methoxy-N,N-dimethyl-[1,1-biphenyl]-3-carboxamide

(293) ##STR00138##

(294) Under an argon atmosphere, a solution of 4-methoxy-3-(N-(3-((2-methoxy-3,4-dioxocyclobut-1-en-1-yl)amino)phenyl)sulfamoyl)-N,N-dimethyl-[1,1-biphenyl]-3-carboxamide (10.1 mg) in ethanol (1.0 mL) were added DIPEA (50.0 L) and m-toluidine (3.0 L), and the mixture was stirred with heating under reflux for 8 hr. The reaction mixture was concentrated under reduced pressure, the obtained residue was crudely purified by silica gel column chromatography (eluent: chloroform/ethyl acetate=4/1), and the crude product was recrystallized from chloroform to give 3-(N-(3-((3,4-dioxo-2-(m-tolylamino)cyclobut-1-en-1-yl)amino)phenyl)sulfamoyl)-4-methoxy-N,N-dimethyl-[1,1-biphenyl]-3-carboxamide (150.2 mg) as colorless needle crystals.

(295) The compounds (Examples 81-84) described in the following Table 11 were also synthesized similarly from aniline having the corresponding R group.

(296) ##STR00139##

(297) TABLE-US-00011 TABLE 11 structure of Ex. substituent on No. aniline .sup.1H-NMR 79 0 1H NMR (400 MHz, Acetone-d6) 8.11 (d, J = 2.8 Hz, 1H), 7.88 (dd, J = 8.4, 2.4 Hz, 1H), 7.67 (dt, J = 8.0, 2.0 Hz, 1H), 7.63 (t, J = 1.6 Hz, 1H), 7.51 (t, J = 8.0 Hz, 1H), 7.43 (m, 1H), 7.39 (d, J = 8.4 Hz, 1H), 7.29 (d, J = 8.8 Hz, 1H), 7.23-7.16 (m, 2H), 7.05 (dt, J = 7.6, 2.0 Hz, 1H), 4.44 (s, 3H), 4.06 (s, 3H), 3.03 (s, 6H). 80 1H NMR (400 MHz, Methanol-d) 8.09 (d, J = 2.4 Hz, 1H), 7.80 (dd, J = 8.4, 2.4 Hz, 1H), 7.63 (d, J = 8.0 Hz, 1H), 7.56 (s, 1H), 7.49 (t, J = 7.6 Hz, 1H), 7.39 (s, 1H), 7.35 (d, J = 7.6 Hz, 1H), 7.30 (s, 1H), 7.27-7.13 (m, 5H), 6.89 (t, J = 8.4 Hz, 2H), 4.02 (s, 3H), 3.09 (s, 3H), 2.99 (s, 6H), 2.31 (s, 3H). 81 1H NMR (400 MHz, DMSO-d6) 10.26 (s, 1H), 9.78 (s, 1H), 9.71 (s, 1H), 8.02 (d, J = 2.4 Hz, 1H), 7.91 (dd, J = 8.4, 2.0 Hz, 1H), 7.67 (d, J = 7.6 Hz, 1H), 7.58 (s, 1H), 7.49 (t, J = 7.6 Hz, 1H), 7.38-7.34 (m, 4H), 7.28 (d, J = 8.4 Hz, 1H), 7.18 (t, J = 8.0 Hz, 1H), 7.09 (s, 1H), 6.94 (d, J = 8.8 Hz, 2H), 6.81 (d, J = 8.4 Hz, 1H), 3.94 (s, 3H), 3.73 (s, 3H), 2.97 (s, 3H), 2.89 (s, 3H). 82 1H NMR (400 MHz, Chloroform-d) 9.29 (brs, 1H), 9.21 (s, 1H), 7.94 (s, 1H), 7.56 (d, J = 9.2 Hz, 1H), 7.51 (s, 1H), 7.42 (d, J = 7.6 Hz, 1H), 7.34-7.22 (m, 4H), 7.10-7.01 (m, 3H), 6.89 (m, 1H), 6.78-6.74 (m, 3H), 6.55 (d, J = 7.6 Hz, 1H), 4.05 (s, 3H), 3.74 (s, 3H), 3.18 (s, 3H), 3.04 (s, 3H). 83 1H NMR (400 MHz, Methanol-d) 8.10 (s, 1H), 7.90 (m, 1H), 7.80 (d, J = 8.4 Hz, 1H), 7.63 (d, J = 7.2 Hz, 1H), 7.56 (s, 1H), 7.49 (t, J = 7.6 Hz, 1H), 7.40 (s, 1H), 7.35 (d, J = 7.6 Hz, 1H), 7.24- 7.16 (m, 3H), 7.07 (m, 1H), 7.01 (m, 1H), 6.95-6.88 (m, 2H), 4.03 (s, 3H), 3.92 (s, 3H), 3.09 (s, 3H), 3.00 (s, 6H). 84 1H NMR (400 MHz, DMSO-d6) 10.27 (s, 1H), 9.77 (s, 1H), 9.70 (s, 1H), 7.99 (d, J = 1.6 Hz, 1H), 7.88 (dd, J = 8.4, 2.0 Hz, 1H), 7.64 (d, J = 8.0 Hz, 1H), 7.55 (s, 1H), 7.46 (t, J = 7.6 Hz, 1H), 7.35-7.30 (m, 4H), 7.25 (d, J = 8.8 Hz, 1H), 7.17-7.12 (m, 3H), 7.05 (s, 1H), 6.78 (d, J = 8.0 Hz, 1H), 3.90 (s, 3H), 2.94 (s, 3H), 2.86 (s, 3H), 2.23 (s, 3H).

Production Example (7)

(298) ##STR00146##

(1) 4-methoxy-3-(N-(3-(3-methoxyphenylsulfonamido)phenyl)sulfamoyl)-N,N-dimethyl-[1,1-biphenyl]-3-carboxamide

(299) ##STR00147##

(300) Under an argon atmosphere, to a solution of 3-(N-(3-aminophenyl)sulfamoyl)-4-methoxy-N,N-dimethyl-[1,1-biphenyl]-3-carboxamide hydrochloride (19.1 mg) in dichloromethane (3.0 mL) were added TEA (23.9 L) and 3-methoxybenzenesulfonyl chloride (7.0 L), and the mixture was stirred at room temperature overnight. Thereto was added sodium triacetoxyborohydride (10 mg), and the mixture was further stirred for 14 hr. The reaction mixture was concentrated under reduced pressure, and the residue was diluted with chloroform and extracted with pure water. The organic layer was washed with saturated brine, dried over sodium sulfate and filtered, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (eluent: ethyl acetate) to give 4-methoxy-3-(N-(3-(3-methoxyphenylsulfonamido)phenyl)sulfamoyl)-N,N-dimethyl-[1,1-biphenyl]-3-carboxamide (19.9 mg).

(301) The compounds described in the following Table 12 were also synthesized similarly from sulfonyl chloride having the corresponding R group.

(302) ##STR00148##

(303) TABLE-US-00012 TABLE 12 Ex. NHSO.sub.2R moiety No. structure .sup.1H-NMR 85 1H NMR (400 MHz, DMSO-d6) 8.17-8.10 (m, 2H), 7.74 (ddd, J = 7.8, 1.9, 1.1 Hz, 1H), 7.68-7.64 (m, 1H), 7.59- 7.49 (m, 3H), 7.45-7.39 (m, 2H), 7.37- 7.29 (m, 2H), 7.17-7.11 (m, 2H), 7.03-6.99 (m, 1H), 6.94 (t, J = 2.1 Hz, 1H), 3.78 (s, 3H), 3.74 (s, 3H), 3.01 (s, 3H), 2.93 (s, 3H). 86 0 1H NMR (400 MHz, Chloroform-d) 8.03 (d, J = 2.4 Hz, 1H), 7.92 (t, J = 1.8 Hz, 1H), 7.78 (ddd, J = 8.0, 1.9, 1.0 Hz, 1H), 7.73 (dd, J = 8.6, 2.4 Hz, 1H), 7.68 (ddd, J = 8.0, 1.8, 1.0 Hz, 1H), 7.55-7.49 (m, 2H), 7.42 (ddd, J = 7.6, 0.8 Hz, 1H), 7.39-7.33 (m, 3H), 7.23- 7.18 (m, 1H), 7.09 (d, J = 8.7 Hz, 1H), 6.99 (s, 1H), 6.89 (t, J = 2.0 Hz, 1H), 6.64 (ddd, J = 7.8, 2.1, 1.2 Hz, 1H), 4.06 (s, 3H), 3.09 (s, 3H), 2.94 (s, 3H). 87 1H NMR (400 MHz, DMSO-d6) 9.71 (s, 1H), 7.93 (d, J = 2.4 Hz, 1H), 7.86 (dd, J = 8.7, 2.4 Hz, 1H), 7.63 (dt, J = 7.9, 2.0, 1.2 Hz, 1H), 7.54 (dd, J = 1.6 Hz, 1H), 7.47 (dd, J = 7.6 Hz, 1H), 7.32 (ddd, J = 7.5, 1.3 Hz, 1H), 7.23 (d, J = 8.7 Hz, 1H), 6.73 (dd, J = 8.0 Hz, 1H), 6.37 (dd, J = 2.0 Hz, 1H), 6.22 (ddd, J = 8.0, 1.9, 0.8 Hz, 1H), 6.09 (ddd, J = 8.0, 2.3, 0.7 Hz, 1H), 5.02 (s, 2H), 3.90 (s, 3H), 3.24 (s, 6H), 2.96 (s, 3H), 2.88 (s, 3H). 88 1H NMR (400 MHz, Chloroform-d) 8.31 (d, J = 2.4 Hz, 1H), 7.85 (dd, J = 8.6, 2.4 Hz, 1H), 7.68 (d, J = 7.3 Hz, 2H), 7.63 (dt, J = 6.6, 1.6 Hz, 2H), 7.51- 7.46 (m, 3H), 7.46-7.41 (m, 3H), 7.39 (dt, J = 7.6, 1.3 Hz, 1H), 7.34-7.28 (m, 1H), 7.16 (ddd, J = 5.9, 3.5, 2.1 Hz, 1H), 7.11 (d, J = 8.7 Hz, 1H), 6.90 (dd, J = 1.3 Hz, 1H), 3.86 (s, 3H), 3.14 (s, 3H), 3.02 (s, 3H). 89 1H NMR (400 MHz, Chloroform-d) 8.22 (d, J = 2.3 Hz, 1H), 7.82 (dd, J = 8.6, 2.4 Hz, 1H), 7.64-7.52 (m, 4H), 7.52- 7.43 (m, 3H), 7.37 (ddd, J = 7.5, 1.2 Hz, 1H), 7.11 (d, J = 8.7 Hz, 1H), 3.90 (s, 3H), 3.32 (s, 3H), 3.14 (s, 3H), 3.01 (s, 3H). 90 1H NMR (400 MHz, DMSO-d6) 10.20 (s, 1H), 10.09 (s, 1H), 10.04 (s, 1H), 7.98 (d, J = 2.4 Hz, 1H), 7.88 (dd, J = 8.7, 2.4 Hz, 1H), 7.67 (ddd, J = 7.8, 1.1 Hz, 1H), 7.60 (dd, J = 1.5 Hz, 1H), 7.51 (dd, J = 7.7 Hz, 1H), 7.37 (ddd, J = 7.6, 1.2 Hz, 1H), 7.22 (d, J = 8.8 Hz, 1H), 7.06 (dd, J = 8.2 Hz, 1H), 7.01 (dd, J = 7.7 Hz, 2H), 6.96 (dd, J = 2.0 Hz, 1H), 6.88 (s, 1H), 6.86-6.80 (m, 2H), 6.78-6.69 (m, 2H), 3.86 (s, 3H), 3.01 (s, 3H), 2.91 (s, 3H), 2.18 (s, 3H).

Production Example (8)

(304) ##STR00155##

(1) tert-butyl (2-((3-nitrophenyl)amino)ethyl)carbamate

(305) ##STR00156##

(306) Under an argon atmosphere, to 3-fluoronitrobenzene (3.21 mL) was added ethylenediamine (25.0 mL), and the mixture was stirred at 100 C. for 24 hr. To the reaction mixture was added saturated aqueous sodium hydrogen carbonate solution, and the mixture was extracted with chloroform. The organic layer was dried over sodium sulfate and filtered, and the filtrate was concentrated. To a solution of the obtained residue in dichloromethane (50 mL) were added triethylamine (4.60 mL) and di-tert-butyl dicarbonate (6.55 g), and the mixture was stirred at room temperature for 2 hr. To the reaction mixture was added saturated aqueous sodium hydrogen carbonate solution, and the mixture was extracted with chloroform. The organic layer was dried over sodium sulfate and filtered, and the filtrate was concentrated. The obtained residue was purified by silica gel column chromatography (eluent: ethyl acetate/hexane=1/4.fwdarw.1/3) to give tert-butyl (2-((3-nitrophenyl)amino)ethyl)carbamate (5.31 g).

(2) tert-butyl (2-((3-aminophenyl)(benzyl)amino)ethyl)carbamate

(307) ##STR00157## (i) Under an argon atmosphere, to a solution of tert-butyl (2-((3-nitrophenyl)amino)ethyl)carbamate (4.46 g) in dichloromethane (30.0 mL) were added 50 wt % aqueous sodium hydroxide solution (10.0 mL), benzyl bromide (2.84 mL) and tetrabutylammonium iodide (587.0 mg), and the mixture was stirred at room temperature for 48 hr. To the reaction mixture was added saturated aqueous sodium hydrogen carbonate solution, and the mixture was extracted with chloroform. The organic layer was dried over sodium sulfate and filtered, and the filtrate was concentrated. The obtained residue was purified by silica gel column chromatography (eluent: ethyl acetate/hexane=1/6.fwdarw.1/4) to give tert-butyl (2-((benzyl)(3-nitrophenyl)amino)ethyl)carbamate (4.62 g). (ii) Under an argon atmosphere, to a suspension of tert-butyl (2-((benzyl)(3-nitrophenyl)amino)ethyl)carbamate in a mixture of ethanol (50.0 mL) and water (20.0 mL) were added ammonium chloride (6.69 g) and iron powder (4.86 g), and the mixture was heated under reflux for 2 hr. The reaction mixture was filtered through celite, and the filtrate was concentrated. Saturated aqueous sodium hydrogen carbonate solution was added, and the mixture was extracted with chloroform. The organic layer was dried over sodium sulfate and filtered, and the filtrate was concentrated. The obtained residue was purified by amine silica gel column chromatography (eluent: chloroform/ethyl acetate=2/1) to give tert-butyl (2-((3-aminophenyl)(benzyl)amino)ethyl)carbamate (4.58 g).

(3) tert-butyl (2-((benzyl)(3-(5-bromo-2-methoxyphenylsulfonamido)phenyl)amino)ethyl)carbamate

(308) ##STR00158##

(309) Under an argon atmosphere, to a solution of tert-butyl (2-((3-aminophenyl)(benzyl)amino)ethyl)carbamate (1.59 g) in dichloromethane (20.0 mL) were added pyridine (413 L) and 5-bromo-2-methoxybenzenesulfonyl chloride (1.33 g), and the mixture was stirred at room temperature overnight. To the reaction mixture was added saturated aqueous sodium hydrogen carbonate solution, and the mixture was extracted with chloroform. The organic layer was dried over sodium sulfate and filtered, and the filtrate was concentrated. The obtained residue was purified by silica gel column chromatography (eluent: ethyl acetate/hexane=1/2) to give tert-butyl (2-((benzyl)(3-(5-bromo-2-methoxyphenylsulfonamido)phenyl)amino)ethyl)carbamate (2.53 g).

(4) tert-butyl (2-((benzyl)(3-(3-(dimethylcarbamoyl)-4-methoxy-[1,1-biphenyl]-3-ylsulfonamido)phenyl)amino)ethyl)carbamate

(310) ##STR00159##

(311) Under an argon atmosphere, to a solution of tert-butyl (2-((benzyl)(3-(5-bromo-2-methoxyphenylsulfonamido)phenyl)amino)ethyl)carbamate (4.66 g) in DME (80.0 mL) were added 3-(N,N-dimethylaminocarbonyl)phenylboronic acid (3.56 g), sodium carbonate (1.80 g), water (8.0 mL) and tetrakis(triphenylphosphine)palladium (463.2 mg), and the mixture was heated under reflux overnight. The reaction mixture was filtered through celite, and the filtrate was concentrated. The obtained residue was purified by silica gel column chromatography (eluent: ethyl acetate/hexane=7/5.fwdarw.1/1) to give tert-butyl (2-((benzyl)(3-(3-(dimethylcarbamoyl)-4-methoxy-[1,1-biphenyl]-3-ylsulfonamido)phenyl)amino)ethyl)carbamate (4.85 g).

(5) 3-(N-(3-((2-aminoethyl)amino)phenyl)sulfamoyl)-4-methoxy-N,N-dimethyl-[1,1-biphenyl]-3-carboxamide dihydrochloride

(312) ##STR00160## (i) To a solution of tert-butyl (2-((benzyl)(3-(3-(dimethylcarbamoyl)-4-methoxy-[1,1-biphenyl]-3-ylsulfonamido)phenyl)amino)ethyl)carbamate (1.50 g) in methanol (30.0 mL) was added palladium hydroxide (221.0 mg), and the mixture was stirred under a hydrogen atmosphere at room temperature for 3 hr. The reaction mixture was filtered through celite, and the filtrate was concentrated. The obtained residue was purified by silica gel column chromatography (eluent: ethyl acetate) to give tert-butyl (2-((3-(3-(dimethylaminocarbamoyl)-4-methoxy-[1,1-biphenyl]-3-ylsulfonamido)phenyl)amino)ethyl)carbamate (950.0 mg). (ii) To tert-butyl (2-((3-(3-(dimethylaminocarbamoyl)-4-methoxy-[1,1-biphenyl]-3-ylsulfonamido)phenyl)amino)ethyl)carbamate (203.0 mg) was added 10% hydrogen chloride-methanol solution (4.0 mL), and the mixture was stirred at 50 C. for 2 hr. The reaction mixture was concentrated to give 3-(N-(3-((2-aminoethyl)amino)phenyl)sulfamoyl)-4-methoxy-N,N-dimethyl-[1,1-biphenyl]-3-carboxamide dihydrochloride (187.0 mg).

(6) 4-methoxy-N,N-dimethyl-3-(N-(3-((2-(3-methylbenzamido)ethyl)amino)phenyl)sulfamoyl)-[1,1-biphenyl]-3-carboxamide

(313) ##STR00161##

(314) Under an argon atmosphere, to a solution of 3-(N-(3-((2-aminoethyl)amino)phenyl)sulfamoyl)-4-methoxy-N,N-dimethyl-[1,1-biphenyl]-3-carboxamide dihydrochloride (127.8 mg) in dichloromethane (14.0 mL) were added 3-toluic acid (32.1 mg), TEA (108.0 L) and BOP (114.8 mg), and the mixture was stirred at room temperature overnight. To the reaction mixture was added saturated aqueous sodium hydrogen carbonate solution, and the mixture was extracted with chloroform. The organic layer was washed with 1N hydrochloric acid and saturated brine, dried over sodium sulfate and filtered, and the filtrate was concentrated. The obtained residue was purified by silica gel column chromatography (eluent: ethyl acetate) to give 4-methoxy-N,N-dimethyl-3-(N-(3-((2-(3-methylbenzamido)ethyl)amino)phenyl)sulfamoyl)-[1,1-biphenyl]-3-carboxamide (19.5 mg).

(7) 4-methoxy-N,N-dimethyl-3-(N-(3-(3-(3-methylbenzoyl)imidazolidin-1-yl)phenyl)sulfamoyl)-[1,1-biphenyl]-3-carboxamide

(315) ##STR00162##

(316) Under an argon atmosphere, to a solution of 4-methoxy-N,N-dimethyl-3-(N-(3-((2-(3-methylbenzamido)ethyl)amino)phenyl)sulfamoyl)-[1,1-biphenyl]-3-carboxamide (19.5 mg) in acetic acid (1.0 mL) was added para-formaldehyde (30.0 mg), and the mixture was stirred at room temperature overnight. The reaction mixture was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (eluent: ethyl acetate) to give 4-methoxy-N,N-dimethyl-3-(N-(3-(3-(3-methylbenzoyl)imidazolidin-1-yl)phenyl)sulfamoyl)-[1,1-biphenyl]-3-carboxamide (14.5 mg).

Production Example (9)

(317) ##STR00163##

(1) ethyl 2-((3-((tert-butoxycarbonyl)amino)phenyl)amino)acetate

(318) ##STR00164##

(319) Under an argon atmosphere, to a solution of tert-butyl (3-aminophenyl)carbamate (1.22 g) in ethanol (10.0 mL) were added sodium acetate (790.0 mg) and ethyl chloroacetate (562 L), and the mixture was stirred at room temperature for 12 hr. The reaction mixture was concentrated under reduced pressure, and the residue was diluted with chloroform and extracted with pure water. The organic layer was washed with saturated brine, dried over sodium sulfate and filtered, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (eluent: hexane/ethyl acetate=4/1.fwdarw.3/2) to give ethyl 2-((3-((tert-butoxycarbonyl)amino)phenyl)amino)acetate (1.40 g).

(2) 2-((3-((tert-butoxycarbonyl)amino)phenyl)amino)acetic acid

(320) ##STR00165##

(321) To a solution of ethyl 2-((3-((tert-butoxycarbonyl)amino)phenyl)amino)acetate (103.3 mg) in ethanol (10.0 mL) was added 1N aqueous sodium hydroxide solution (3.5 mL), and the mixture was stirred at room temperature for 6 hr. To the reaction mixture was added 1N aqueous hydrochloric acid solution, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over magnesium sulfate and filtered, and the filtrate was concentrated under reduced pressure to give 2-((3-((tert-butoxycarbonyl)amino)phenyl)amino)acetic acid (99.1 mg). The present compound was used for the next reaction without further purification.

(3) tert-butyl (3-((2-((3-methylbenzyl)amino)-2-oxoethyl)amino)phenyl)carbamate

(322) ##STR00166##

(323) Under an argon atmosphere, to a solution of 2-((3-((tert-butoxycarbonyl)amino)phenyl)amino)acetic acid (15.0 mg) in dichloromethane (5.0 mL) were added DIPEA (87.0 L) and HATU (190.0 mg), and the mixture was stirred at room temperature for 10 min. 3-Methylbenzylamine (12.0 L) was added, and the mixture was further stirred for 10 hr. The reaction mixture was concentrated under reduced pressure, and the residue was diluted with chloroform, and extracted with saturated aqueous sodium hydrogen carbonate solution. The organic layer was washed with saturated brine, dried over sodium sulfate and filtered, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (eluent: hexane/ethyl acetate=4/1.fwdarw.1/1) to give tert-butyl (3-((2-((3-methylbenzyl)amino)-2-oxoethyl)amino)phenyl)carbamate (13.0 mg).

(4) 4-methoxy-N,N-dimethyl-3-(N-(3-((2-((3-methylbenzyl)amino)-2-oxoethyl)amino)phenyl)sulfamoyl)-[1,1-biphenyl]-3-carboxamide

(324) ##STR00167## (i) Under an argon atmosphere, to a solution of tert-butyl (3-((2-((3-methylbenzyl)amino)-2-oxoethyl)amino)phenyl)carbamate (13.0 mg) in dichloromethane (2.0 mL) was added TFA (200 L), and the mixture was stirred at room temperature for 2 hr. The reaction mixture was concentrated under reduced pressure to give 2-((3-aminophenyl)amino)-N-(3-methylbenzyl)acetamide TFA salt (13.0 mg). The present compound was used for the next reaction without further purification. (ii) Under an argon atmosphere, to a solution of 2-((3-aminophenyl)amino)-N-(3-methylbenzyl)acetamide TFA salt (6.8 mg) in pyridine (1.0 mL) was added 3-(dimethylcarbamoyl)-4-methoxy-[1,1-biphenyl]-3-sulfonyl chloride (6.0 mg), and the mixture was stirred at room temperature for 16 hr. The reaction mixture was concentrated under reduced pressure, and the obtained residue was purified by silica gel column chromatography (eluent: hexane/ethyl acetate=1/9.fwdarw.0/1) to give 4-methoxy-N,N-dimethyl-3-(N-(3-((2-((3-methylbenzyl)amino)-2-oxoethyl)amino)phenyl)sulfamoyl)-[1,1-biphenyl]-3-carboxamide (7.0 mg).

Production Example (10)

(325) ##STR00168##

(1) 3-(N-(3-(N-(2-acrylamidoethyl)acrylamido)phenyl)sulfamoyl)-4-methoxy-N,N-dimethyl-[1,1-biphenyl]-3-carboxamide

(326) ##STR00169##

(327) Under an argon atmosphere, to a solution of 3-(N-(3-((2-aminoethyl)amino)phenyl)sulfamoyl)-4-methoxy-N,N-dimethyl-[1,1-biphenyl]-3-carboxamide dihydrochloride (100.0 mg) in dichloromethane (1.0 mL) were added DIPEA (64.0 L) and acryloyl chloride (30.0 L), and the mixture was stirred at room temperature overnight. The reaction mixture was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (eluent: ethyl acetate/methanol=1/0.fwdarw.9/1) to give 3-(N-(3-(N-(2-acrylamidoethyl)acrylamido)phenyl)sulfamoyl)-4-methoxy-N,N-dimethyl-[1,1-biphenyl]-3-carboxamide (103.0 mg).

Production Example (11)

(328) ##STR00170##

(1) (E)-3-(N-(3-((4-(dimethylamino)-2-(hydroxymethyl)phenyl)diazenyl)phenyl)sulfamoyl)-4-methoxy-N,N-dimethyl-[1,1-biphenyl]-3-carboxamide

(329) ##STR00171##

(330) To a mixture of 3-(N-(3-aminophenyl)sulfamoyl)-4-methoxy-N,N-dimethyl-[1,1-biphenyl]-3-carboxamide hydrochloride (30.0 mg), sulfuric acid on silica gel (50.0 mg) and sodium nitrite (10.0 mg) was added pure water (50.0 L), and the mixture was stirred for 10 min until the release of gas ceased. Thereto was added 3-(dimethylaminobenzyl)alcohol (10.0 mg), and the mixture was stirred at room temperature for 1 hr. The reaction mixture was dried in vacuo, and purified by silica gel column chromatography (eluent: hexane/ethyl acetate=1/0.fwdarw.2/1) to give (E)-3-(N-(3-((4-(dimethylamino)-2-(hydroxymethyl)phenyl)diazenyl)phenyl)sulfamoyl)-4-methoxy-N,N-dimethyl-[1,1-biphenyl]-3-carboxamide (10.9 mg).

(331) The compound of Example 98 described in the following Table 13 was also synthesized similarly from corresponding benzene derivative.

Production Example (12)

(332) ##STR00172##

(1) 4-methoxy-N,N-dimethyl-3-(N-(3-(methylamino)phenyl)sulfamoyl)-[1,1-biphenyl]-3-carboxamide

(333) ##STR00173##

(334) To a suspension of 3-(N-(3-aminophenyl)sulfamoyl)-4-methoxy-N,N-dimethyl-[1,1-biphenyl]-3-carboxamide hydrochloride (100.0 mg) in methanol (15.0 mL) were added TEA (100.0 L), para-formaldehyde (10.0 mg) and 5% palladium-activated carbon (9.20 mg), and the mixture was stirred with heating under reflux under a hydrogen atmosphere for 3 hr. The reaction mixture was filtered through celite, and the filtrate was concentrated. The obtained residue was purified by preparative thin layer chromatography (eluent: chloroform/methanol=20/1) to give 4-methoxy-N,N-dimethyl-3-(N-(3-(methylamino)phenyl)sulfamoyl)-[1,1-biphenyl]-3-carboxamide (74.8 mg).

Production Example (13)

(335) ##STR00174##

(1) 3-(N-(3-(dimethylamino)phenyl)sulfamoyl)-4-methoxy-N,N-dimethyl-[1,1-biphenyl]-3-carboxamide

(336) ##STR00175##

(337) To a suspension of 3-(N-(3-aminophenyl)sulfamoyl)-4-methoxy-N,N-dimethyl-[1,1-biphenyl]-3-carboxamide hydrochloride (17.0 mg) in ethanol (1.50 mL) were added TEA (20.0 L), 30% aqueous formalin solution (14.0 L) and 5% palladium-activated carbon (9.20 mg), and the mixture was stirred under a hydrogen atmosphere with heating under reflux for 40 hr. To the reaction mixture was added acetic acid (20.0 L), and the mixture was further stirred for 12 hr. The reaction mixture was filtered through celite, and the filtrate was diluted with chloroform, and extracted with saturated aqueous sodium hydrogen carbonate solution. The organic layer was washed with saturated brine, dried over sodium sulfate and filtered, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by preparative thin layer chromatography (eluent: chloroform/methanol=40/1) to give 3-(N-(3-(dimethylamino)phenyl)sulfamoyl)-4-methoxy-N,N-dimethyl-[1,1-biphenyl]-3-carboxamide (14.0 mg).

(338) ##STR00176##

(339) TABLE-US-00013 TABLE 13 structure of Ex. substituent on No. aniline .sup.1H-NMR 91 1H NMR (400 MHz, Chloroform-d) 7.98 (d, J = 2.4 Hz, 1H), 7.67 (dd, J = 8.4, 2.0 Hz, 1H), 7.53 (s, 1H), 7.51 (d, J = 8.8 Hz, 1H), 7.42 (t, J = 7.6 Hz, 1H), 7.34 (d, J = 7.6 Hz, 1H), 7.22-7.14 (m, 3H), 7.05 (d, J = 7.6 Hz, 2H), 7.00-6.94 (m, 2H), 6.87 (s, 1H), 6.44 (t, J = 7.6 Hz, 2H), 6.38 (s, 1H), 4.63 (m, 1H), 4.44 (s, 2H), 3.87 (s, 3H), 3.45-3.42 (m, 2H), 3.24-3.19 (m, 2H), 3.12 (s, 3H), 2.98 (s, 3H), 1.38 (s, 9H). 92 1H NMR (400 MHz, Chloroform-d) 8.06 (d, J = 2.4 Hz, 1H), 7.70 (dd, J = 8.6, 2.4 Hz, 1H), 7.56 (dd, J = 1.5 Hz, 1H), 7.52 (ddd, J = 7.8, 1.5 Hz, 1H), 7.42 (dd, J = 7.6 Hz, 1H), 7.32 (ddd, J = 7.5, 1.3 Hz, 1H), 7.14 (dd, J = 7.8 Hz, 1H), 7.07 (d, J = 8.7 Hz, 1H), 7.05- 6.98 (m, 2H), 6.97-6.89 (m, 4H), 6.47 (dd, J = 7.5, 2.1 Hz, 1H), 6.37 (dd, J = 2.1 Hz, 1H), 6.32 (dd, J = 8.4, 2.5 Hz, 1H), 4.36 (d, J = 5.9 Hz, 2H), 4.05 (s, 3H), 3.70 (d, J = 4.3 Hz, 2H), 3.12 (s, 3H), 2.99 (s, 3H), 2.25 (s, 3H). 93 1H NMR (400 MHz, Chloroform-d) 8.02 (brs, J = 16.5 Hz, 1H), 7.77-7.62 (brm, 1H), 7.59-7.47 (brm, 2H), 7.42 (d, J = 7.7 Hz, 1H), 7.37-7.23 (brm, 5H), 7.16 (brd, J = 11.0 Hz, 1H), 7.10- 6.94 (brm, 2H), 6.55-6.39 (brm, 2H), 6.39-6.27 (brm, 1H), 4.86 (brs, 1H), 4.58 (brs, 1H), 4.10-3.92 (brm, 4H), 3.78 (dd, J = 7.1 Hz, 1H), 3.42 (brs, J = 6.6 Hz, 2H), 3.10 (brs, 3H), 2.98 (s, 3H), 2.37 (s, 3H). 94 0 1H NMR (400 MHz, Chloroform-d) 8.04 (d, J = 2.4 Hz, 1H), 7.96 (brs, 1H), 7.70 (dd, J = 8.6, 2.4 Hz, 1H), 7.54- 7.48 (m, 2H), 7.42 (dd, J = 7.8 Hz, 1H), 7.33 (ddd, J = 7.5, 1.3 Hz, 1H), 7.22 (d, J = 7.8 Hz, 1H), 7.17 (ddd, J = 8.2, 1.5 Hz, 1H), 7.05 (d, J = 8.7 Hz, 1H), 6.95 (dd, J = 1.8 Hz, 1H), 6.87-6.79 (m, 2H), 6.25-5.99 (m, 3H), 5.67 (dd, J = 16.7, 10.3 Hz, 1H), 5.59-5.49 (m, 1H), 5.32 (d, J = 10.3 Hz, 1H), 4.00 (s, 3H), 3.82 (t, J = 5.9 Hz, 2H), 3.35 (q, J = 5.2 Hz, 2H), 3.11 (s, 3H), 2.98 (s, 3H). 95 1H NMR (400 MHz, Chloroform-d) 8.06 (d, J = 2.4 Hz, 1H), 7.70 (dd, J = 8.6, 2.4 Hz, 1H), 7.57-7.51 (m, 2H), 7.43 (ddd, J = 7.4, 1.2 Hz, 1H), 7.35 (ddd, J = 7.5, 1.4 Hz, 1H), 7.07 (d, J = 8.7 Hz, 1H), 6.96 (dd, J = 8.0 Hz, 1H), 6.90 (brs, 1H), 6.44 (dd, J = 2.2 Hz, 1H), 6.36-6.24 (m, 2H), 4.07 (s, 3H), 3.13 (s, 3H), 3.00 (s, 3H), 2.74 (s, 3H). 96 1H NMR (400 MHz, Chloroform-d) 8.07 (d, J = 2.4 Hz, 1H), 7.69 (dd, J = 8.6, 2.4 Hz, 1H), 7.55-7.49 (m, 2H), 7.43 (ddd, J = 7.4, 1.0 Hz, 1H), 7.35 (ddd, J = 7.5, 1.4 Hz, 1H), 7.06 (d, J = 8.7 Hz, 1H), 7.04-6.97 (m, 2H), 6.51 (dd, J = 2.2 Hz, 1H), 6.44-6.38 (m, 1H), 6.38- 6.31 (m, 1H), 4.06 (s, 3H), 3.13 (s, 3H), 2.99 (s, 3H), 2.85 (s, 6H). 97 1H NMR (400 MHz, Chloroform-d) 8.08 (d, J = 2.4 Hz, 1H), 7.80 (d, J = 9.3 Hz, 1H), 7.70 (dd, J = 8.6, 2.4 Hz, 1H), 7.56-7.49 (m, 3H), 7.44-7.39 (m, 2H), 7.36-7.31 (m, 2H), 7.26-7.22 (m, 1H), 7.16 (s, 1H), 7.09 (d, J = 8.7 Hz, 1H), 6.68-6.61 (m, 2H), 4.89 (s, 2H), 4.11 (s, 3H), 3.10 (s, 9H), 2.97 (s, 3H). 98 1H NMR (400 MHz, Chloroform-d) 9.73 (s, 1H), 8.08 (d, J = 2.3 Hz, 1H), 7.89 (d, J = 2.5 Hz, 1H), 7.71-7.62 (m, 2H), 7.54-7.46 (m, 4H), 7.39 (dd, J = 7.6 Hz, 1H), 7.36-7.28 (m, 3H), 7.20 (brd, J = 7.3 Hz, 1H), 7.11-6.98 (m, 2H), 6.53 (dd, J = 8.9, 2.6 Hz, 1H), 4.05 (s, 3H), 3.12 (s, 3H), 2.98 (s, 3H), 1.50 (s, 9H). 99 1H NMR (400 MHz, DMSO-d6) 10.33 (brs, 1H), 8.01 (d, J = 2.4 Hz, 1H), 7.93 (dd, J = 8.7, 2.4 Hz, 1H), 7.69 (ddd, J = 7.8, 1.9, 1.1 Hz, 1H), 7.60 (dd, J = 1.6 Hz, 1H), 7.52 (dd, J = 7.7 Hz, 1H), 7.37 (ddd, J = 7..6, 1.3 Hz, 1H), 7.28 (d, J = 8.8 Hz, 1H), 7.17 (dd, J = 8.0 Hz, 1H), 6.99 (brs, 1H), 6.90 (brd, J = 8.5 Hz, 1H), 6.72 (brd, J = 7.8 Hz, 1H), 3.92 (s, 3H), 3.00 (s, 3H), 2.92 (s, 3H).

Production Example (14)

(340) ##STR00186##

(1) 3-(chlorosulfonyl)-4-methoxybenzoic acid

(341) ##STR00187##

(342) Under an argon atmosphere, to chlorosulfonic acid (2.20 mL) was slowly added 4-methoxybenzoic acid (1.00 g) under ice-cooling, and the mixture was stirred for 10 min. Thereafter, the reaction mixture was heated to 65 C. and stirred for 2 hr. The reaction mixture was allowed to cool, poured into ice and stirred for 1 hr. The resulting white solid was collected by filtration and washed with cold water. The obtained solid was dried in vacuo to give 3-(chlorosulfonyl)-4-methoxybenzoic acid (966.0 mg). The present compound was used for the next reaction without further purification.

(2) 1-(3-aminophenyl)-3-(3-(dimethylamino)phenyl)urea

(343) ##STR00188## (i) Under an argon atmosphere, to a solution of 3-dimethylaminobenzoic acid (1.59 g) in benzene (10.0 mL) were added TEA (2.60 mL) and DPPA (4.0 mL), and the mixture was stirred under reflux at 110 C. for 1 hr. To the reaction mixture was added tert-butyl (3-aminophenyl)carbamate (1.31 g), and the mixture was further stirred under reflux for 10 hr. The reaction mixture was allowed to cool and concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (eluent: ethyl acetate/chloroform=0/1.fwdarw.5/1) to give tert-butyl (3-(3-(3-(dimethylamino)phenyl)ureido)phenyl)carbamate (3.43 g). (ii) Under an argon atmosphere, to a suspension of tert-butyl (3-(3-(3-(dimethylamino)phenyl)ureido)phenyl)carbamate (1.0 g) in dichloromethane (10.0 mL) was added TFA (600 L), and the mixture was stirred overnight. The reaction mixture was concentrated under reduced pressure, and the residue was diluted with 25% methanol-containing chloroform and extracted with saturated aqueous sodium hydrogen carbonate solution. The organic layer was washed with saturated brine, dried over sodium sulfate and filtered, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (eluent: chloroform/ethyl acetate=2/1) to give 1-(3-aminophenyl)-3-(3-(dimethylamino)phenyl)urea (715.3 mg).

(3) 3-(N-(3-(3-(3-(dimethylamino)phenyl)ureido)phenyl)sulfamoyl)-4-methoxybenzoic acid

(344) ##STR00189##

(345) Under an argon atmosphere, pyridine (7.5 mL) was added to a suspension of 1-(3-aminophenyl)-3-(3-(dimethylamino)phenyl)urea (797.1 mg) in dichloromethane (7.5 mL) and completely dissolved by agitating at 60 C. under reflux. The reaction mixture was allowed to cool, a solution of 3-(chlorosulfonyl)-4-methoxybenzoic acid (672.9 mg) in 50% pyridine-containing dichloromethane (15 mL) was slowly added dropwise, and the mixture was stirred at room temperature for 15 hr. Furthermore, 3-(chlorosulfonyl)-4-methoxybenzoic acid (448.8 mg) was added and the mixture was stirred at room temperature for 19 hr. The reaction mixture was concentrated under reduced pressure, and the obtained residue was purified by silica gel column chromatography (eluent: chloroform/ethyl acetate/methanol=2/1/0.fwdarw.1/1/0.fwdarw.1/1/0.4) to give 3-(N-(3-(3-(3-(dimethylamino)phenyl)ureido)phenyl)sulfamoyl)-4-methoxybenzoic acid (905.6 mg).

(4) N-benzyl-3-(N-(3-(3-(3-(dimethylamino)phenyl)ureido)phenyl)sulfamoyl)-4-methoxybenzamide

(346) ##STR00190##

(347) Under an argon atmosphere, to a solution of 3-(N-(3-(3-(3-(dimethylamino)phenyl)ureido)phenyl)sulfamoyl)-4-methoxybenzoic acid (15.4 mg) in dichloromethane (3.0 mL) were added TEA (20.1 L) and HATU (25.9 mg), and the mixture was stirred at room temperature for 10 min. Benzylamine (4.0 L) was added and the mixture was further stirred for 12 hr. The reaction mixture was concentrated under reduced pressure, and the residue was diluted with chloroform and extracted with saturated aqueous sodium hydrogen carbonate solution. The organic layer was washed with saturated brine, dried over sodium sulfate and filtered, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by preparative thin layer chromatography (eluent: chloroform/ethyl acetate=1/2) to give N-benzyl-3-(N-(3-(3-(3-(dimethylamino)phenyl)ureido)phenyl)sulfamoyl)-4-methoxybenzamide (3.9 mg).

(348) The compounds described in the following Table 14 were also synthesized similarly from amine having the corresponding R and R groups.

(349) ##STR00191##

(350) TABLE-US-00014 TABLE 14 amide Ex. substituent No. structure .sup.1H-NMR 100 1H NMR (400 MHz, Methanol-d4) 8.40 (d, J = 2.3 Hz, 1H), 8.03 (dd, J = 8.7, 2.3 Hz, 1H), 7.50 (dd, J = 2.0 Hz, 1H), 7.33- 7.17 (m, 6H), 7.09 (ddd, J = 10.9, 8.1 Hz, 2H), 6.95 (ddd, J = 8.2, 2.1, 1.0 Hz, 1H), 6.90 (dd, J = 2.1 Hz, 1H), 6.75 (ddd, J = 8.0, 2.1, 1.0 Hz, 1H), 6.70 (ddd, J = 7.9, 1.9, 0.8 Hz, 1H), 6.48 (dd, J = 8.3, 2.5 Hz, 1H), 4.44 (s, 2H), 4.05 (s, 3H), 2.92 (s, 6H). 101 1H NMR (400 MHz, Methanol-d4) 7.84 (d, J = 2.0 Hz, 1H), 7.65-7.46 (m, 1H), 7.39-6.81 (m, 11H), 6.78-6.59 (m, 2H), 6.44 (dd, J = 7.9, 2.4 Hz, 1H), 4.63 (brs, 1.2H), 4.31 (brs, 0.8H), 4.00 (s, 3H), 3.41 (brs, 0.8H), 3.06 (brs, 1.2H), 2.89 (s, 6H), 1.11 (brs, 1.2H), 0.95 (brs, 1.8H). 102 1H NMR (400 MHz, DMSO-d6) 10.11 (brs, 1H), 8.61-8.43 (m, 2H), 7.75 (d, J = 2.1 Hz, 1H), 7.62 (brs, 2H), 7.35 (dd, J = 7.7, 4.8 Hz, 1H), 7.21 (d, J = 7.3 Hz, 2H), 7.13-6.94 (m, 3H), 6.86 (s, 1H), 6.75-6.59 (m, 2H), 6.35 (dd, J = 8.3, 2.3 Hz, 1H), 4.61 (s, 1H), 3.94 (s, 3H), 3.09 (brs, 2H), 2.86 (s, 6H), 0.95 (brs, 3H). 103 1H NMR (400 MHz, DMSO-d6) 10.03 (brs, 1H), 9.16 (dd, J = 5.9 Hz, 1H), 8.64 (s, 1H), 8.52 (d, J = 1.9 Hz, 1H), 8.48- 8.39 (m, 2H), 8.31 (d, J = 2.3 Hz, 1H), 8.08 (dd, J = 8.7, 2.2 Hz, 1H), 7.68 (ddd, J = 7.9, 1.9 Hz, 1H), 7.32 (dd, J = 7.8, 4.7 Hz, 1H), 7.29-7.20 (m, 2H), 7.12-7.02 (m, 3H), 6.85 (t, J = 2.1 Hz, 1H), 6.74-6.64 (m, 2H), 6.35 (dd, J = 8.3, 2.3 Hz, 1H), 4.44 (d, J = 5.7 Hz, 2H), 3.97 (s, 3H), 2.86 (s, 6H). 104 1H NMR (400 MHz, Chloroform-d) 8.36 (brs, 1H), 8.04-7.79 (m, 2H), 7.73- 7.48 (m, 4H), 7.08 (dd, J = 8.1 Hz, 1H), 6.94 (dd, J = 8.0 Hz, 1H), 6.87 (brd, J = 8.6 Hz, 1H), 6.80 (brd, J = 8.3 Hz, 1H), 6.72 (brs, 1H), 6.65 (brd, J = 6.9 Hz, 1H), 6.56 (brd, J = 7.9 Hz, 1H), 6.42 (dd, J = 8.4, 1.9 Hz, 1H), 5.15 (brs, 1H), 3.90 (s, 3H), 3.30 (q, J = 5.4 Hz, 2H), 3.09 (d, J = 6.1 Hz, 2H), 2.85 (s, 6H), 1.69-1.51 (m, 2H), 1.42 (s, 9H). 105 1H NMR (400 MHz, Chloroform-d) 8.38 (brs, 1H), 8.05-7.41 (m, 6H), 7.10 (dd, J = 8.0 Hz, 1H), 6.94 (dd, J = 8.0 Hz, 1H), 6.90-6.64 (m, 3H), 6.64- 6.35 (m, 3H), 5.26 (s, 1H), 3.89 (s, 3H), 3.39 (brd, J = 5.4 Hz, 2H), 3.26 (brd, 2H), 2.87 (s, 6H), 1.38 (s, 9H). 106 1H NMR (400 MHz, Chloroform-d) 8.80 (brs, 1H), 8.41 (d, J = 1.6 Hz, 1H), 8.10-7.87 (m, 2H), 7.65 (brs, 1H), 7.30 (brs, 1H), 7.18-7.04 (m, 4H), 7.00-6.91 (m, 2H), 6.87 (d, J = 8.8 Hz, 1H), 6.71 (d, J = 7.6 Hz, 1H), 6.62 (brd, J = 9.0 Hz, 1H), 6.56 (brs, 1H), 6.51-6.40 (m, 3H), 3.90 (s, 3H), 2.88 (s, 6H), 2.83 (s, 6H). 107 1H NMR (400 MHz, Methanol-d4) 8.21 (d, J = 2.4 Hz, 1H), 8.01 (dd, J = 8.7, 2.4 Hz, 1H), 7.40 (dd, J = 2.1 Hz, 1H), 7.22 (d, J = 8.8 Hz, 1H), 7.10 (d, J = 8.0 Hz, 1H), 7.04 (dd, J = 8.0 Hz, 1H), 6.96 (ddd, J = 8.2, 2.0, 1.0 Hz, 1H), 6.90 (dd, J = 2.2 Hz, 1H), 6.76 (ddd, J = 8.0, 2.1, 1.0 Hz, 1H), 6.68 (ddd, J = 7.9, 1.9, 0.7 Hz, 1H), 6.47 (ddd, J = 8.3, 2.5, 0.6 Hz, 1H), 4.05 (s, 3H), 3.22 (s, 2H), 2.91 (s, 6H), 2.35 (s, 6H), 2.31 (s, 2H), 0.93 (s, 6H).

Production Example (15)

(351) ##STR00200##

(1) 1-(3-aminophenyl)-3-(4-(dimethylamino)phenyl)urea

(352) ##STR00201## (i) Under an argon atmosphere, to a solution of 4-dimethylaminobenzoic acid (1.60 g) in benzene (10.0 mL) were added TEA (2.60 mL) and DPPA (4.10 mL), and the mixture was stirred at 110 C. under reflux for 1 hr. To the reaction mixture was further added tert-butyl (3-aminophenyl)carbamate (1.35 g), and the mixture was further stirred under reflux for 10 hr. The reaction mixture was allowed to cool and concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (eluent: ethyl acetate/chloroform=0/1.fwdarw.4/1) to give tert-butyl (3-(3-(4-(dimethylamino)phenyl)ureido)phenyl)carbamate (1.90 g). (ii) Under an argon atmosphere, to a suspension of tert-butyl (3-(3-(4-(dimethylamino)phenyl)ureido)phenyl)carbamate (1.90 g) in dichloromethane (10.0 mL) was added TFA (2.00 mL), and the mixture was stirred overnight. The reaction mixture was concentrated under reduced pressure, and the residue was diluted with 15% methanol-containing chloroform, and extracted with saturated aqueous sodium hydrogen carbonate solution. The organic layer was washed with saturated brine, dried over sodium sulfate and filtered, and the filtrate was concentrated under reduced pressure to give 1-(3-aminophenyl)-3-(4-(dimethylamino)phenyl)urea (1.02 g). The present compound was used for the next reaction without further purification.

(2) 3-(N-(3-(3-(4-(dimethylamino)phenyl)ureido)phenyl)sulfamoyl)-4-methoxybenzoic acid

(353) ##STR00202##

(354) Under an argon atmosphere, DIPEA (1.80 mL) was added to a suspension of 1-(3-aminophenyl)-3-(4-(dimethylamino)phenyl)urea (916.7 mg) in dichloromethane (10.0 mL) and completely dissolved. Thereto was slowly added 3-(chlorosulfonyl)-4-methoxybenzoic acid (1.09 g), and the mixture was stirred at room temperature for 3 hr. The reaction mixture was concentrated under reduced pressure, and the obtained residue was purified by silica gel column chromatography (eluent: chloroform/methanol=20/1.fwdarw.10/1) to give 3-(N-(3-(3-(4-(dimethylamino)phenyl)ureido)phenyl)sulfamoyl)-4-methoxybenzoic acid (1.26 g).

(3) N-benzyl-3-(N-(3-(3-(4-(dimethylamino)phenyl)ureido)phenyl)sulfamoyl)-4-methoxybenzamide

(355) ##STR00203##

(356) Under an argon atmosphere, to a solution of 3-(N-(3-(3-(4-(dimethylamino)phenyl)ureido)phenyl)sulfamoyl)-4-methoxybenzoic acid (22.8 mg) in dichloromethane (5.0 mL) were added TEA (40.0 L) and HATU (37.8 mg), and the mixture was stirred at room temperature for 10 min. Thereto was added benzylamine (5.7 L), and the mixture was further stirred for 15 hr. The reaction mixture was concentrated under reduced pressure, and the residue was diluted with chloroform and extracted with saturated aqueous sodium hydrogen carbonate solution. The organic layer was washed with saturated brine, dried over sodium sulfate and filtered, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by preparative thin layer chromatography (eluent: chloroform/ethyl acetate=1/2) to give N-benzyl-3-(N-(3-(3-(4-(dimethylamino)phenyl)ureido)phenyl)sulfamoyl)-4-methoxybenzamide (2.80 mg).

(357) The compounds described in the following Table 15 were also synthesized similarly from amine having the corresponding R and R groups.

(358) ##STR00204##

(359) TABLE-US-00015 TABLE 15 Ex. No. amide substituent structure .sup.1H-NMR 108 05 1H NMR (400 MHz, Methanol-d4) 8.38 (d, J = 2.3 Hz, 1H), 8.00 (dd, J = 8.7, 2.4 Hz, 1H), 7.52 (dd, J = 2.0 Hz, 1H), 7.32- 7.23 (m, 4H), 7.20 (t, J = 8.8 Hz, 4H), 7.05 (dd, J = 8.1 Hz, 1H), 6.87 (ddd, J = 8.1, 2.1, 0.9 Hz, 1H), 6.76- 6.68 (m, 3H), 4.36 (s, 2H), 4.02 (s, 3H), 2.85 (s, 6H). 109 06 1H NMR (400 MHz, Methanol-d4) 8.44- 8.36 (m, 3H), 8.00 (dd, J = 8.7, 2.4 Hz, 1H), 7.70 (ddd, J = 7.9, 1.9 Hz, 1H), 7.64 (dd, J = 2.1 Hz, 1H), 7.36 (dd, J = 7.8, 4.9 Hz, 1H), 7.25-7.16 (m, 3H), 7.05 (dd, J = 8.1 Hz, 1H), 6.80 (ddd, J = 8.2, 2.0, 0.9 Hz, 1H), 6.72 (d, J = 9.0 Hz, 2H), 6.68 (ddd, J = 8.0, 2.1, 0.8 Hz, 1H), 4.32 (s, 2H), 4.03 (s, 3H), 2.85 (s, 6H). 110 07 1H NMR (400 MHz, Methanol-d4) 7.87 (d, J = 2.2 Hz, 1H), 7.62 (brs, 1H), 7.38- 7.17 (m, 8H), 7.15-6.87 (m, 3H), 6.78 (d, J = 9.0 Hz, 2H), 6.72 (brs, 1H), 4.71 (brs, 1.2H), 4.35 (brs, 0.8H), 4.03 (s, 3H), 3.43 (brs, 0.8H), 3.09 (brs, 1.2H), 2.88 (s, 6H), 1.14 (brs, 1.2H), 0.98 (brs, 1.8H). 111 08 1H NMR (400 MHz, Methanol-d4) 8.67- 8.36 (m, 2H), 7.88-7.73 (m, 1H), 7.61 (brs, 1H), 7.40 (dd, J = 7.9, 5.2 Hz, 1H), 7.34 (dd, J = 2.1 Hz, 1H), 7.28- 7.08 (m, 4H), 7.00 (brs, 2H), 6.84- 6.65 (m, 3H), 4.70 (brs, 2H), 4.03 (s, 3H), 3.17 (brs, 2H), 2.88 (s, 6H), 1.05 (brs, 3H).

Production Example (16)

(360) ##STR00209##

(1) 1-(3-aminophenyl)-3-(2-(dimethylamino)phenyl)urea

(361) ##STR00210## (i) Under an argon atmosphere, to a solution of 2-dimethylaminobenzoic acid (900.0 mg) in benzene (8.0 mL) were added TEA (1.49 mL) and DPPA (2.30 mL), and the mixture was stirred at 110 C. under reflux for 5 hr. To the reaction mixture was added tert-butyl (3-aminophenyl)carbamate (655.7 mg), and the mixture was stirred under reflux for 2 hr. The reaction mixture was allowed to cool and concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (eluent: ethyl acetate/chloroform=0/1.fwdarw.4/1) to give tert-butyl (3-(3-(2-(dimethylamino)phenyl)ureido)phenyl)carbamate (1.12 g). (ii) Under an argon atmosphere, to a suspension of tert-butyl (3-(3-(2-(dimethylamino)phenyl)ureido)phenyl)carbamate (1.00 g) in dichloromethane (10.0 mL) was added TFA (2.00 mL), and the mixture was stirred overnight. The reaction mixture was concentrated under reduced pressure, and the residue was diluted with 15% methanol-containing chloroform and extracted with saturated aqueous sodium hydrogen carbonate solution. The organic layer was washed with saturated brine, dried over sodium sulfate and filtered, and the filtrate was concentrated under reduced pressure to give 1-(3-aminophenyl)-3-(2-(dimethylamino)phenyl)urea (725.8 mg). The present compound was used for the next reaction without further purification.

(2) 3-(N-(3-(3-(2-(dimethylamino)phenyl)ureido)phenyl)sulfamoyl)-4-methoxybenzoic acid

(362) ##STR00211##

(363) Under an argon atmosphere, pyridine (10.0 mL) was added to a suspension of 1-(3-aminophenyl)-3-(2-(dimethylamino)phenyl)urea (686.6 mg) in dichloromethane (10.0 mL) and completely dissolved. Thereto was slowly added 3-(chlorosulfonyl)-4-methoxybenzoic acid (524.4 mg), and the mixture was heated under reflux at 50 C. for 3 hr. The reaction mixture was concentrated under reduced pressure, and the obtained residue was purified by silica gel column chromatography (eluent: chloroform/ethyl acetate=1/0.fwdarw.1/1) to give 3-(N-(3-(3-(2-(dimethylamino)phenyl)ureido)phenyl)sulfamoyl)-4-methoxybenzoic acid (258.6 mg).

(3) tert-butyl (3-(3-(N-(3-(3-(2-(dimethylamino)phenyl)ureido)phenyl)sulfamoyl)-4-methoxybenzamido)propyl)carbamate

(364) ##STR00212##

(365) Under an argon atmosphere, to a solution of 3-(N-(3-(3-(2-(dimethylamino)phenyl)ureido)phenyl)sulfamoyl)-4-methoxybenzoic acid (17.7 mg) in dichloromethane (3.0 mL) were added TEA (20.0 L) and HATU (35.2 mg), and the mixture was stirred at room temperature for 10 min. Thereto was added N-(tert-butoxycarbonyl)-1,3-diaminopropane (7.0 L), and the mixture was further stirred for 8 hr. The reaction mixture was concentrated under reduced pressure, and the residue was diluted with chloroform and extracted with saturated aqueous sodium hydrogen carbonate solution. The organic layer was washed with saturated brine, dried over sodium sulfate and filtered, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by preparative thin layer chromatography (eluent: chloroform/ethyl acetate=1/1) to give tert-butyl (3-(3-(N-(3-(3-(2-(dimethylamino)phenyl)ureido)phenyl)sulfamoyl)-4-methoxybenzamido)propyl)carbamate (17.9 mg).

(366) The compounds described in the following Table 16 were also synthesized similarly from amine having the corresponding R and R groups.

(367) ##STR00213##

(368) TABLE-US-00016 TABLE 16 amide Ex. substituent No. structure .sup.1H-NMR 112 1H NMR (400 MHz, Methanol-d4) 8.35 (d, J = 2.3 Hz, 1H), 8.02 (dd, J = 8.0, 1.5 Hz, 1H), 7.99 (dd, J = 8.7, 2.3 Hz, 1H), 7.48 (brs, 1H), 7.24-7.14 (m, 2H), 7.12-7.03 (m, 2H), 7.03-6.95 (m, 2H), 6.75 (brd, J = 7.9 Hz, 1H), 6.55 (brs, 1H), 4.04 (s, 3H), 3.35-3.25 (m, 2H), 3.04 (q, J = 6.5 Hz, 2H), 2.64 (s, 6H), 1.66 (p, J = 6.8 Hz, 2H), 1.41 (s, 9H). 113 .sup.1H NMR (400 MHz, Methanol-d.sub.4) 8.50 (brs, 1H), 8.43 (d, J = 5.9 Hz, 1H), 8.02 (d, J = 7.8 Hz, 1H), 7.88 (d, J = 1.9 Hz, 1H), 7.81 (brs, 1H), 7.62 (brs, 1H), 7.44-7.34 (m, 2H), 7.22 (brd, J = 8.8 Hz, 1H), 7.19 (dd, J = 7.8, 1.5 Hz, 1H), 7.12-7.00 (m, 3H), 6.97 (ddd, J = 7.6, 1.6 Hz, 1H), 6.73 (brs, 1H), 4.69 (brs, 2H), 4.04 (s, 3H), 3.17 (brs, 1H), 2.63 (s, 6H), 1.06 (brs, 3H). 114 .sup.1H NMR (400 MHz, DMSO-d.sub.6) 10.11 (brs, 1H), 9.45 (s, 1H), 8.32 (s, 1H), 8.07 (dd, J = 8.1, 1.4 Hz, 1H), 7.77 (d, J = 2.2 Hz, 1H), 7.61 (dd, J = 8.6, 2.2 Hz, 1H), 7.27 (dd, J = 1.8 Hz, 1H), 7.21 (d, J = 8.7 Hz, 1H), 7.17 (dd, J = 7.9, 1.4 Hz, 1H), 7.14 (ddd, J = 8.2, 1.9, 0.9 Hz, 1H), 7.04 (dd, J = 8.0 Hz, 1H), 7.01 (ddd, J = 8.0, 1.5 Hz, 1H), 6.93 (ddd, J = 7.6, 1.6 Hz, 1H), 6.67 (ddd, J = 8.0, 1.9, 0.9 Hz, 1H), 3.94 (s, 3H), 2.86 (brd, J = 33.6 Hz, 6H), 2.60 (s, 6H).

Production Example (17)

(369) ##STR00217##

(1) 3-(N-(3-(3-(3-(dimethylamino)phenyl)ureido)phenyl)sulfamoyl)-4-hydroxy-N,N-dimethyl-[1,1-biphenyl]-3-carboxamide

(370) ##STR00218##

(371) Under an argon atmosphere, to a suspension of 3-(N-(3-(3-(3-(dimethylamino)phenyl)ureido)phenyl)sulfamoyl)-4-methoxy-N,N-dimethyl-[1,1-biphenyl]-3-carboxamide (6.5 mg) in dichloromethane (15.0 mL) was added boron tribromide (100.0 L) under ice-cooling, and the mixture was stirred at room temperature for 12 hr. The reaction mixture was diluted with 20% methanol-containing chloroform and extracted with saturated aqueous sodium hydrogen carbonate solution under ice-cooling. The organic layer was washed with saturated brine, dried over sodium sulfate and filtered, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by preparative thin layer chromatography (eluent: chloroform/methanol=10/1) to give 3-(N-(3-(3-(3-(dimethylamino)phenyl)ureido)phenyl)sulfamoyl)-4-hydroxy-N,N-dimethyl-[1,1-biphenyl]-3-carboxamide (1.9 mg).

Production Example (18)

(372) ##STR00219##

(1) 3-bromo-N-(3-(3-(3-(dimethylamino)phenyl)ureido)phenyl)benzenesulfonamide

(373) ##STR00220##

(374) Under an argon atmosphere, to a solution of 1-(3-aminophenyl)-3-(3-(dimethylamino)phenyl)urea (348.0 mg) in dehydrated dichloromethane (6.4 mL) were added pyridine (2.6 mL) and 3-bromobenzenesulfonyl chloride (223.0 L), and the mixture was stirred at room temperature for 45 min. The reaction mixture was concentrated under reduced pressure, and the obtained residue was purified by silica gel column chromatography (eluent: chloroform/ethyl acetate/methanol=5/1/0.fwdarw.1/1/0.fwdarw.10/0/1) to give 3-bromo-N-(3-(3-(3-(dimethylamino)phenyl)ureido)phenyl)benzenesulfonamide (21.8 mg).

(2) 3-(N-(3-(3-(3-(dimethylamino)phenyl)ureido)phenyl)sulfamoyl)-N,N-dimethyl-[1,1-biphenyl]-3-carboxamide

(375) ##STR00221##

(376) Under an argon atmosphere, to a solution of 3-bromo-N-(3-(3-(3-(dimethylamino)phenyl)ureido)phenyl)benzenesulfonamide (19.6 mg) in DME (3.0 mL) were added 3-(N,N-dimethylaminocarbonyl)phenylboronic acid (13.3 mg), sodium carbonate (8.5 mg), water (0.10 mL) and tetrakis(triphenylphosphine)palladium (2.3 mg), and the mixture was heated under reflux for 3 hr. To the reaction mixture was added saturated aqueous sodium hydrogen carbonate solution, and the mixture was extracted with chloroform. The organic layer was dried over sodium sulfate and filtered, and the filtrate was concentrated. The obtained residue was purified by preparative thin layer chromatography (eluent: chloroform/ethyl acetate=1/1) to give 3-(N-(3-(3-(3-(dimethylamino)phenyl)ureido)phenyl)sulfamoyl)-N,N-dimethyl-[1,1-biphenyl]-3-carboxamide (19.7 mg).

(377) The compounds (Examples 117 and 118) described in the following Table 17 were also synthesized similarly from sulfonyl chloride having the corresponding R group.

Production Example (19)

(378) ##STR00222##

(1) 4-hydroxy-N,N-dimethyl-[1,1-biphenyl]-3-carboxamide

(379) ##STR00223##

(380) Under an argon atmosphere, to a solution of 4-bromophenol (1.03 g) in DME (25.0 mL) were added 3-(N,N-dimethylaminocarbonyl)phenylboronic acid (1.04 g), sodium carbonate (1.12 g), water (2.50 mL) and tetrakis(triphenylphosphine)palladium (219.3 mg), and the mixture was heated under reflux for 16 hr. To the reaction mixture was added pure water, and the mixture was extracted with chloroform. The organic layer was dried over sodium sulfate and filtered, and the filtrate was concentrated. The obtained residue was purified by silica gel column chromatography (eluent: hexane/ethyl acetate=4/1.fwdarw.1/1) to give 4-hydroxy-N,N-dimethyl-[1,1-biphenyl]-3-carboxamide (459.8 mg).

(2) 4-ethoxy-N,N-dimethyl-[1,1-biphenyl]-3-carboxamide

(381) ##STR00224##

(382) Under an argon atmosphere, to a solution of 4-hydroxy-N,N-dimethyl-[1,1-biphenyl]-3-carboxamide (60.9 mg) in acetone (5.0 mL) were added potassium carbonate (350.3 mg) and ethyl iodide (44.0 L), and the mixture was stirred at room temperature for 22 hr. To the reaction mixture was added pure water, and the mixture was extracted with chloroform. The organic layer was dried over sodium sulfate and filtered, and the filtrate was concentrated. The obtained residue was purified by preparative thin layer chromatography (eluent: chloroform/ethyl acetate=1/1) to give 4-ethoxy-N,N-dimethyl-[1,1-biphenyl]-3-carboxamide (68.2 mg).

(3) 3-(dimethylcarbamoyl)-4-ethoxy-[1,1-biphenyl]-3-sulfonyl chloride

(383) ##STR00225##

(384) Under an argon atmosphere, to chlorosulfonic acid (150.0 L) was slowly added a solution of 4-ethoxy-N,N-dimethyl-[1,1-biphenyl]-3-carboxamide (61.1 mg) in dichloromethane (2.0 mL), and the mixture was stirred under ice-cooling for 10 min. The reaction mixture was warmed to room temperature and stirred for 1 hr, thionyl chloride (320.0 L) and DMF (50 L) were added, and the mixture was stirred at 60 C. for 2 hr. The reaction mixture was allowed to cool, poured into ice, stirred for 20 min, and extracted with chloroform. The organic layer was dried over sodium sulfate and filtered, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (eluent: ethyl acetate/hexane=1/2) to give 3-(dimethylcarbamoyl)-4-ethoxy-[1,1-biphenyl]-3-sulfonyl chloride (79.7 mg).

(4) 3-(N-(3-(3-(3-(dimethylamino)phenyl)ureido)phenyl)sulfamoyl)-4-ethoxy-N,N-dimethyl-[1,1-biphenyl]-3-carboxamide

(385) ##STR00226##

(386) Under an argon atmosphere, to a solution of 1-(3-aminophenyl)-3-(3-(dimethylamino)phenyl)urea TFA salt (9.3 mg) in dehydrated dichloromethane (2.0 mL) were added pyridine (130.0 L) and 3-(dimethylcarbamoyl)-4-ethoxy-[1,1-biphenyl]-3-sulfonyl chloride (14.3 mg), and the mixture was stirred at room temperature overnight. The reaction mixture was concentrated under reduced pressure, and the obtained residue was purified by preparative thin layer chromatography (eluent: chloroform/ammonia-saturated chloroform=40/1) to give 3-(N-(3-(3-(3-(dimethylamino)phenyl)ureido)phenyl)sulfamoyl)-4-ethoxy-N,N-dimethyl-[1,1-biphenyl]-3-carboxamide (15.4 mg).

(387) The compound of Example 120 described in the following Table 17 was also synthesized similarly from alkylhalide having the corresponding R group.

(388) ##STR00227##

(389) TABLE-US-00017 TABLE 17 Ex. R moiety No. structure .sup.1H-NMR 115 1H NMR (400 MHz, Chloroform-d) 7.76 (s, 1H), 7.60 (d, J = 8.8 Hz, 1H), 7.58 (s, 1H), 7.40-7.38 (m, 3H), 7.32-7.24 (m, 4H), 7.06-6.97 (m, 3H), 6.91-6.87 (m, 2H), 6.83 (d, J = 7.6 Hz, 1H), 6.75 (s, 1H), 6.48 (d, J = 7.6 Hz, 1H), 6.39 (dd, J = 8.0, 2.0 Hz, 1H), 3.14 (s, 3H), 2.99 (s, 3H), 2.83 (s, 6H). 116 1H NMR (400 MHz, Chloroform-d) 7.90- 7.83 (m, 2H), 7.75 (brd, J = 8.0 Hz, 1H), 7.60 (brd, J = 7.9 Hz, 1H), 7.53- 7.47 (m, 3H), 7.41 (dd, J = 7.8 Hz, 1H), 7.38-7.33 (m, 2H), 7.12-7.03 (m, 2H), 6.99 (brs, J = 8.1 Hz, 1H), 6.86 (brd, J = 8.2 Hz, 1H), 6.73 (brs, 1H), 6.50 (dd, J = 7.7, 1.4 Hz, 1H), 6.45 (dd, J = 8.3, 2.3 Hz, 1H), 3.15 (s, 3H), 3.00 (s, 3H), 2.87 (s, 6H). 117 0 1H NMR (400 MHz, Chloroform-d) 8.76 (brs, 1H), 8.15 (s, 1H), 7.93 (s, 1H), 7.61-7.45 (m, 4H), 7.45-7.30 (m, 3H), 7.24-7.20 (m, 1H), 7.07 (dd, J = 8.1 Hz, 1H), 6.96 (dd, J = 8.1 Hz, 1H), 6.84 (d, J = 7.9 Hz, 1H), 6.77 (d, J = 7.4 Hz, 1H), 6.71 (s, 1H), 6.51 (d, J = 7.7 Hz, 1H), 6.43 (dd, J = 8.3, 2.1 Hz, 1H), 3.13 (s, 3H), 2.99 (s, 3H), 2.84 (s, 6H), 2.62 (s, 3H). 118 1H NMR (400 MHz, DMSO-d6) 10.70 (s, 1H), 8.65 (s, 1H), 8.38 (s, 1H), 8.26 (d, J = 2.2 Hz, 1H), 7.94 (dd, J = 8.4, 2.3 Hz, 1H), 7.79 (d, J = 7.7 Hz, 1H), 7.72 (d, J = 8.3 Hz, 1H), 7.65 (s, 1H), 7.51-7.40 (m, 3H), 7.14-6.99 (m, 3H), 6.82-6.78 (m, 1H), 6.72 (ddd, J = 15.8, 8.0, 1.7 Hz, 2H), 6.36 (dd, J = 8.4, 2.3 Hz, 1H), 2.98 (s, 3H), 2.89 (s, 3H), 2.85 (s, 6H). 119 1H NMR (400 MHz, DMSO-d6) 9.97 (s, 1H), 8.61 (s, 1H), 8.37 (s, 1H), 8.32 (s, 1H), 8.04 (d, J = 2.4 Hz, 1H), 7.88 (dd, J = 8.7, 2.4 Hz, 1H), 7.71 (ddd, J = 7.8, 1.4 Hz, 1H), 7.58 (dd, J = 1.5 Hz, 1H), 7.46 (dd, J = 7.7 Hz, 1H), 7.39- 7.32 (m, 2H), 7.27 (d, J = 8.8 Hz, 1H), 7.10-6.99 (m, 3H), 6.83 (t, J = 2.1 Hz, 1H), 6.72 (ddd, J = 7.3, 2.0 Hz, 1H), 6.69 (dd, J = 8.0, 1.2 Hz, 1H), 6.35 (dd, J = 8.2, 2.3 Hz, 1H), 4.25 (q, J = 7.0 Hz, 2H), 2.98 (s, 3H), 2.89 (s, 3H), 2.86 (s, 6H), 1.38 (t, J = 7.0 Hz, 3H). 120 1H NMR (400 MHz, Chloroform-d) 7.98 (d, J = 2.3 Hz, 1H), 7.68 (d, J = 4.8 Hz, 2H), 7.55-7.46 (m, 2H), 7.42 (d, J = 7.6 Hz, 1H), 7.36-7.26 (m, 4H), 7.00 (dd, J = 8.1 Hz, 1H), 6.92 (d, J = 8.7 Hz, 1H), 6.88 (dd, J = 8.1 Hz, 1H), 6.79- 6.67 (m, 3H), 6.47 (d, J = 7.8 Hz, 1H), 6.35 (dd, J = 8.3, 2.1 Hz, 1H), 4.10 (t, J = 6.7 Hz, 2H), 3.13 (s, 3H), 2.97 (s, 3H), 2.80 (s, 6H), 1.92 (h, J = 7.2 Hz, 2H), 1.06 (t, J = 7.4 Hz, 3H).

Production Example (20)

(390) ##STR00234##

(1) 2-methoxy-3-nitrobenzoic acid

(391) ##STR00235## (i) Under an argon atmosphere, to a solution of 2-hydroxy-3-nitrobenzoic acid (1.0 g) in acetone (20.0 mL) were added potassium carbonate (3.70 g) and methyl iodide (1.70 mL), and the mixture was stirred at room temperature overnight. To the reaction mixture was added pure water, and the mixture was extracted with ethyl acetate. The organic layer was dried over sodium sulfate and filtered, and the filtrate was concentrated and dried to give methyl 2-methoxy-3-nitrobenzoate (1.10 g). The present compound was used for the next reaction without further purification. (ii) To a solution of methyl 2-methoxy-3-nitrobenzoate (1.10 g) in ethanol (20.0 mL) was added 1N aqueous sodium hydroxide solution (20.0 mL), and the mixture was stirred at room temperature overnight. To the reaction mixture was added 1N aqueous hydrochloric acid solution, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over magnesium sulfate and filtered, and the filtrate was concentrated under reduced pressure to give 2-methoxy-3-nitrobenzoic acid (980 mg). The present compound was used for the next reaction without further purification.

(2) 1-(3-amino-2-methoxyphenyl)-3-(3-(dimethylamino)phenyl)urea

(392) ##STR00236## (i) Under an argon atmosphere, to a solution of 2-methoxy-3-nitrobenzoic acid (100.0 mg) in toluene (5.0 mL) were added TEA (140.0 L) and DPPA (216.0 L), and the mixture was stirred at 110 C. under reflux for 2 hr. To the reaction mixture was added N,N-dimethyl-1,3-phenylenediamine (106.0 mg), and the mixture was further stirred under reflux for 2 hr. The reaction mixture was allowed to cool, concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (eluent: hexane/ethyl acetate=9/1.fwdarw.1/1.fwdarw.chloroform/methanol=9/1) to give 1-(3-nitro-2-methoxyphenyl)-3-(3-(dimethylamino)phenyl)urea (98.5 mg). (ii) To a solution of 1-(3-nitro-2-methoxyphenyl)-3-(3-(dimethylamino)phenyl)urea (98.5 mg) in methanol (10.0 mL) was added 5% palladium-activated carbon (10.30 mg), and the mixture was stirred under a hydrogen atmosphere at room temperature overnight. The reaction mixture was filtered through celite and the filtrate was concentrated. The obtained residue was purified by silica gel column chromatography (eluent: hexane/ethyl acetate=9/1.fwdarw.1/4) to give 1-(3-amino-2-methoxyphenyl)-3-(3-(dimethylamino)phenyl)urea (80.5 mg).

(3) 3-(N-(3-(3-(3-(dimethylamino)phenyl)ureido)-2-methoxyphenyl)sulfamoyl)-4-methoxy-N,N-dimethyl-[1,1-biphenyl]-3-carboxamide

(393) ##STR00237##

(394) Under an argon atmosphere, to a solution of 1-(3-amino-2-methoxyphenyl)-3-(3-(dimethylamino)phenyl)urea (18.0 mg) in dichloromethane (1.0 mL) were added pyridine (100.0 L) and 3-(dimethylcarbamoyl)-4-methoxy-[1,1-biphenyl]-3-sulfonyl chloride (16.0 mg), and the mixture was stirred at room temperature overnight. The reaction mixture was concentrated under reduced pressure, and the obtained residue was purified by silica gel column chromatography (eluent: chloroform/methanol=49/1.fwdarw.4/1) to give 3-(N-(3-(3-(3-(dimethylamino)phenyl)ureido)-2-methoxyphenyl)sulfamoyl)-4-methoxy-N,N-dimethyl-[1,1-biphenyl]-3-carboxamide (26.8 mg).

(395) Example 121, Example 122 and Example 124 were respectively synthesized by a method similar to Production Example (4) using the corresponding tert-butyl (2-aminophenyl)carbamate, tert-butyl (4-aminophenyl)carbamate and tert-butyl (6-aminopyridin-2-yl)carbamate.

(396) ##STR00238##

(397) TABLE-US-00018 TABLE 18 Ex. R moiety No. structure .sup.1H-NMR 121 1H NMR (400 MHz, Chloroform-d) 8.28 (s, 0.7H), 7.97-7.93 (m, 1H), 7.79 (s, 0.7H), 7.73 (dd, J = 8.6, 2.4 Hz, 0.3H), 7.67 (s, 0.7H), 7.58 (dd, J = 8.6, 2.4 Hz, 0.7H), 7.55 (s, 0.7H), 7.53-7.47 (m, 0.6H), 7.47- 7.40 (m, 0.7H), 7.41-7.34 (m, 1H), 7.33- 7.29 (m, 1H), 7.23 (d, J = 1.7 Hz, 0.3H), 7.18 (dd, J = 7.8, 1.4 Hz, 0.7H), 7.15 (d, J = 8.7 Hz, 0.3H), 7.05 (dd, J = 8.1 Hz, 0.7H), 7.00-6.88 (m, 3.3H), 6.69 (dd, J = 8.0, 1.2 Hz, 0.3H), 6.64 (brs, 0.3H), 6.57 (dd, J = 7.9, 1.4 Hz, 0.3H), 6.53-6.37 (m, 1.7H), 4.10 (s, 0.9H), 3.89 (s, 2.1H), 3.15 (s, 2.1H), 3.11 (s, 0.9H), 3.01 (s, 2.1H), 2.96 (s, 0.9H), 2.87 (s, 6H). 122 0 1H NMR (400 MHz, DMSO-d6) 9.82 (brs, 1H), 8.52-8.42 (m, 2H), 7.94-7.86 (m, 2H), 7.65 (d, J = 8.0 Hz, 1H), 7.56 (s, 1H), 7.50 (dd, J = 7.7 Hz, 1H), 7.36 (d, J = 7.8 Hz, 1H), 7.32-7.20 (m, 4H), 7.07-6.97 (m, 2H), 6.89-6.81 (m, 1H), 6.64 (d, J = 8.1 Hz, 1H), 6.35-6.31 (m, 1H), 3.96 (s, 3H), 2.99 (s, 3H), 2.91 (s, 3H), 2.84 (s, 6H). 123 1H NMR (400 MHz, Chloroform-d) 8.11 (d, J = 2.4 Hz, 1H), 7.77 (dd, J = 8.3, 1.4 Hz, 1H), 7.71 (brs, 1H), 7.67 (dd, J = 1.6 Hz, 1H), 7.61 (dd, J = 8.7, 2.4 Hz, 1H), 7.56 (ddd, J = 8.0, 1.7, 1.3 Hz, 1H), 7.54-7.49 (m, 2H), 7.44 (t, J = 7.7 Hz, 1H), 7.34 (ddd, J = 7.6, 1.3 Hz, 1H), 7.20 (dd, J = 8.3, 1.4 Hz, 1H), 7.14 (dd, J = 8.1 Hz, 1H), 6.97-6.88 (m, 3H), 6.57 (dd, J = 7.6, 1.5 Hz, 1H), 6.47 (dd, J = 8.4, 2.4 Hz, 1H), 3.86 (s, 3H), 3H), 3.70 (s, 3H), 3.20 (s, 3H), 3.05 (s, 3H), 2.92 (s, 6H). 124 1H NMR (400 MHz, DMSO-d6) 9.33 (brs, 1H), 8.01 (d, J = 3.1 Hz, 1H), 7.89 (dd, J = 8.7, 2.2 Hz, 1H), 7.61-7.48 (m, 2H), 7.38- 7.27 (m, 3H), 7.23 (d, J = 8.8 Hz, 1H), 7.15- 7.00 (m, 3H), 6.70 (brs, 1H), 6.57 (d, J = 8.0 Hz, 1H), 6.44 (dd, J = 8.7, 2.7 Hz, 1H), 3.86 (s, 3H), 2.98 (s, 3H), 2.87 (d, J = 7.5 Hz, 9H).

Production Example (21)

(398) ##STR00243##

(1) 3-(N-(3-(3-(3-(dimethylamino)phenyl)-1-methylureido)phenyl)sulfamoyl)-4-methoxy-N,N-dimethyl-[1,1-biphenyl]-3-carboxamide

(399) ##STR00244##

(400) Under an argon atmosphere, to a solution of 3-dimethylaminobenzoic acid (34.0 mg) in benzene (3.0 mL) were added TEA (57.0 L) and DPPA (88.0 L), and the mixture was stirred at 110 C. under reflux for 30 min. To the reaction mixture was added 4-methoxy-N,N-dimethyl-3-(N-(3-(methylamino)phenyl)sulfamoyl)-[1,1-biphenyl]-3-carboxamide (45.0 mg), and the mixture was stirred under reflux for 12 hr. The reaction mixture was allowed to cool, saturated aqueous sodium hydrogen carbonate solution was added and the mixture was extracted with chloroform. The organic layer was washed with saturated brine, dried over sodium sulfate and filtered, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by preparative thin layer chromatography (eluent: chloroform/methanol=30/1) to give 3-(N-(3-(3-(3-(dimethylamino)phenyl)-1-methylureido)phenyl)sulfamoyl)-4-methoxy-N,N-dimethyl-[1,1-biphenyl]-3-carboxamide (14.0 mg).

Production Example (22)

(401) ##STR00245##

(1) 3-(N-(3-(3-(3-(dimethylamino)phenyl)-1,3-dimethylureido)phenyl)sulfamoyl)-4-methoxy-N,N-dimethyl-[1,1-biphenyl]-3-carboxamide

(402) ##STR00246##

(403) Under an argon atmosphere, to a solution of trimethylphenylenediamine (35.0 mg) in 1,2-dichloroethane (2.0 mL) were added DIPEA (52.0 L) and triphosgene (22.0 mg), and the mixture was stirred at room temperature for 30 min. To the reaction mixture was added a solution of 4-methoxy-N,N-dimethyl-3-(N-(3-(methylamino)phenyl)sulfamoyl)-[1,1-biphenyl]-3-carboxamide (33.0 mg) in 1,2-dichloroethane (2.0 mL), and the mixture was stirred with heating under reflux for 5 hr. The reaction mixture was allowed to cool, saturated aqueous sodium hydrogen carbonate solution was added and the mixture was extracted with chloroform. The organic layer was washed with saturated brine, dried over sodium sulfate and filtered, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by preparative thin layer chromatography (eluent: chloroform/methanol=20/1) to give 3-(N-(3-(3-(3-(dimethylamino)phenyl)-1,3-dimethylureido)phenyl)sulfamoyl)-4-methoxy-N,N-dimethyl-[1,1-biphenyl]-3-carboxamide (38.1 mg).

Production Example (23)

(404) ##STR00247##

(1) 3-(N-(3-(3-(3-(dimethylamino)phenyl)-3-methylureido)phenyl)sulfamoyl)-4-methoxy-N,N-dimethyl-[1,1-biphenyl]-3-carboxamide

(405) ##STR00248##

(406) Under an argon atmosphere, to a solution of triphosgene (24.0 mg) in 1,2-dichloroethane (2.0 mL) was added a solution of DIPEA (52.0 L) and trimethylphenylenediamine (39.0 mg) in 1,2-dichloroethane (1.0 mL), and the mixture was stirred at room temperature for 30 min. To the reaction mixture was added a solution of 3-(N-(3-aminophenyl)sulfamoyl)-4-methoxy-N,N-dimethyl-[1,1-biphenyl]-3-carboxamide hydrochloride (38.0 mg) in 1,2-dichloroethane (2.0 mL)/DIPEA (29.0 L), and the mixture was stirred with heating under reflux for 7 hr. The reaction mixture was allowed to cool, saturated aqueous sodium hydrogen carbonate solution was added and the mixture was extracted with chloroform. The organic layer was washed with saturated brine, dried over sodium sulfate and filtered, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by preparative thin layer chromatography (eluent: chloroform/methanol=20/1) to give 3-(N-(3-(3-(3-(dimethylamino)phenyl)-3-methylureido)phenyl)sulfamoyl)-4-methoxy-N,N-dimethyl-[1,1-biphenyl]-3-carboxamide (25.2 mg).

(407) ##STR00249##

(408) TABLE-US-00019 TABLE 19 Ex. urea moiety No. structure .sup.1H-NMR 125 0 1H NMR (400 MHz, Chloroform-d) 8.07 (d, J = 2.4 Hz, 1H), 7.68 (dd, J = 8.6, 2.4 Hz, 1H), 7.55-7.53 (m, 1H), 7.48 (ddd, J = 7.7, 1.6 Hz, 1H), 7.42 (ddd, J = 7.6, 0.5 Hz, 1H), 7.38-7.30 (m, 2H), 7.16 (ddd, J = 8.1, 2.0, 1.1 Hz, 2H), 7.07-6.96 (m, 4H), 6.92 (dd, J = 2.2 Hz, 1H), 6.37 (ddd, J = 8.3, 2.5, 0.8 Hz, 1H), 6.22 (ddd, J = 7.9, 2.0, 0.8 Hz, 1H), 6.03 (s, 1H), 4.03 (s, 3H), 3.22 (s, 3H), 3.13 (s, 3H), 2.98 (s, 3H), 2.90 (s, 6H). 126 1H NMR (400 MHz, Chloroform-d) 8.06 (dd, J = 2.3, 0.8 Hz, 1H), 7.72 (ddd, J = 8.6, 2.4, 0.8 Hz, 1H), 7.56-7.49 (m, 2H), 7.43 (dd, J = 7.6 Hz, 1H), 7.38-7.33 (m, 1H), 7.17 (s, 1H), 7.07 (d, J = 8.7 Hz, 1H), 6.87 (dd, J = 8.2 Hz, 1H), 6.80-6.74 (m, 1H), 6.71 (dd, J = 8.1 Hz, 1H), 6.64 (brs, 1H), 6.46 (dddd, J = 8.0, 1.0 Hz, 1H), 6.27 (dd, J = 8.4, 2.5 Hz, 1H), 6.10 (brs, 1H), 5.89-5.82 (m, 1H), 4.05 (s, 3H), 3.12 (s, 3H), 3.07 (s, 3H), 3.01 (s, 3H), 2.96 (s, 3H), 2.77 (s, 6H). 127 1H NMR (400 MHz, Chloroform-d) 8.01 (d, J = 2.4 Hz, 1H), 7.67 (dd, J = 8.6, 2.4 Hz, 1H), 7.55-7.49 (m, 2H), 7.41 (dd, J = 8.3, 7.6 Hz, 1H), 7.33 (ddd, J = 7.6, 1.4 Hz, 1H), 7.29-7.21 (m, 2H), 7.15 (s, 1H), 7.04 (d, J = 8.7 Hz, 1H), 7.00 (dd, J = 8.1 Hz, 1H), 6.82 (ddd, J = 8.1, 2.1, 0.9 Hz, 1H), 6.76 (ddd, J = 8.1, 2.1, 0.9 Hz, 1H), 6.66 (ddd, J = 8.5, 2.5, 0.8 Hz, 1H), 6.54 (ddd, J = 7.6, 1.9, 0.8 Hz, 1H), 6.52 (dd, J = 2.2 Hz, 1H), 6.39 (s, 1H), 4.05 (s, 3H), 3.26 (s, 3H), 3.11 (s, 3H), 2.97 (s, 3H), 2.94 (s, 6H).

Production Example (24)

(409) ##STR00253##

(1) 1-(3-nitrophenyl)imidazolidin-2-one

(410) ##STR00254##

(411) Under an argon atmosphere, to 3-fluoronitrobenzene (2.20 mL) was added ethylenediamine (2.20 mL), and the mixture was stirred at 100 C. for 16 hr. To the reaction mixture was added water, and the mixture was extracted with chloroform. The organic layer was dried over sodium sulfate and filtered, and the filtrate was concentrated. To a solution of the obtained residue in dry THF (100 mL) was added carbonyldiimidazole (7.56 g) under ice-cooling, and the mixture was stirred for 1 hr. To the reaction mixture was added saturated brine, and the mixture was extracted with ethyl acetate. The organic layer was dried over magnesium sulfate and filtered, and the filtrate was concentrated. The obtained residue was purified by silica gel column chromatography (eluent: methanol/chloroform=5/95) and then recrystallized (ethyl acetate/chloroform=1:1) to give 1-(3-nitrophenyl)imidazolidin-2-one (5.31 g).

(2) 1-(3-nitrophenyl)-3-phenylimidazolidin-2-one

(412) ##STR00255##

(413) Under an argon atmosphere, to a solution of 1-(3-nitrophenyl)imidazolidin-2-one (200 mg) in anhydrous toluene (1.6 mL) were added copper iodide (18.3 mg), N,N-dimethylcyclohexane-1,2-diamine (31.0 L), anhydrous potassium carbonate (333 mg) and bromobenzene (110 L), and the mixture was stirred with heating under reflux for 22 hr. The reaction mixture was allowed to cool, chloroform was added, and the mixture was filtered through celite and washed with chloroform. The filtrate was washed with distilled water and saturated brine, dried over magnesium sulfate and filtered, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (eluent: chloroform) to give 1-(3-nitrophenyl)-3-phenylimidazolidin-2-one (258 mg).

(3) 1-(3-aminophenyl)-3-phenylimidazolidin-2-one

(414) ##STR00256##

(415) To a solution of 1-(3-nitrophenyl)-3-phenylimidazolidin-2-one (237 mg) in ethanol (30.0 mL) was added 5% palladium-activated carbon (89.0 mg), and the mixture was stirred under a hydrogen atmosphere at 50 C. for 2 hr. The reaction mixture was allowed to cool and filtered through celite, and the filtrate was concentrated. The obtained residue was purified by silica gel column chromatography (eluent: methanol/chloroform=2/98) to give 1-(3-aminophenyl)-3-phenylimidazolidin-2-one (178 mg).

(4) 4-methoxy-N,N-dimethyl-3-(N-(3-(2-oxo-3-phenylimidazolidin-1-yl)phenyl)sulfamoyl)-[1,1-biphenyl]-3-carboxamide

(416) ##STR00257##

(417) Under an argon atmosphere, to a solution of 1-(3-aminophenyl)-3-phenylimidazolidin-2-one (30.0 mg) in anhydrous pyridine (1.0 mL) was added 3-(dimethylcarbamoyl)-4-methoxy-[1,1-biphenyl]-3-sulfonyl chloride (43.0 mg), and the mixture was stirred with heating under reflux for 30 min. The reaction mixture was allowed to cool, distilled water was added and the mixture was extracted with chloroform. The organic layer was washed with saturated brine, dried over magnesium sulfate and filtered, and the filtrate was concentrated under reduced pressure. The obtained residue was dissolved in chloroform, hexane was added under ice-cooling, and the resulting precipitate was collected by filtration to give 4-methoxy-N,N-dimethyl-3-(N-(3-(2-oxo-3-phenylimidazolidin-1-yl)phenyl)sulfamoyl)-[1,1-biphenyl]-3-carboxamide (53.5 mg).

(418) The compounds (Examples 129-136) described in the following Table 20 were also synthesized similarly from diamine having the corresponding carbon number (n=1-3) and bromobenzene having R group.

(419) ##STR00258##

(420) TABLE-US-00020 TABLE 20 Ex. urea moiety No. structure .sup.1H-NMR 128 1H NMR (400 MHz, Chloroform-d) 8.04 (d, J = 2.3 Hz, 1H), 7.69 (dd, J = 8.6, 2.3 Hz, 1H), 7.62-7.47 (m, 5H), 7.40 (dd, J = 7.6 Hz, 1H), 7.38-7.30 (m, 3H), 7.19 (dd, J = 7.5 Hz, 2H), 7.09 (dd, J = 7.6 Hz, 2H), 6.98 (s, 1H), 6.85 (ddd, J = 6.8, 1.7 Hz, 1H), 4.11 (s, 3H), 3.98-3.82 (m, 4H), 3.10 (s, 3H), 2.97 (s, 3H). 129 0 1H NMR (400 MHz, DMSO-d6) 10.11 (brs, 1H), 8.02 (s, 1H), 7.89 (d, J = 8.7 Hz, 1H), 7.70 (d, J = 7.2 Hz, 1H), 7.60 (s, 1H), 7.56 (s, 1H), 7.45-7.31 (m, 2H), 7.26 (d, J = 8.6 Hz, 1H), 7.19 (d, J = 7.9 Hz, 2H), 7.17-7.07 (m, 2H), 7.03 (d, J = 8.3 Hz, 1H), 6.96 (dd, J = 7.5 Hz, 1H), 6.79 (d, J = 7.2 Hz, 1H), 3.94 (s, 3H), 3.88-3.78 (m, 2H), 3.78- 3.68 (m, 2H), 2.98 (s, 3H), 2.90 (s, 3H), 2.62 (s, 6H). 130 1H NMR (400 MHz, DMSO-d6) 10.12 (s, 1H), 8.02 (d, J = 2.2 Hz, 1H), 7.90 (dd, J = 8.6, 2.2 Hz, 1H), 7.70 (d, J = 7.8 Hz, 1H), 7.59 (d, J = 14.3 Hz, 2H), 7.45 (dd, J = 7.7 Hz, 1H), 7.35 (d, J = 7.6 Hz, 1H), 7.27 (d, J = 8.7 Hz, 1H), 7.19-7.09 (m, 3H), 7.00 (brs, 1H), 6.83 (d, J = 7.8 Hz, 2H), 6.46 (dd, J = 8.4, 2.2 Hz, 1H), 3.96 (s, 3H), 3.89 (dd, J = 9.6, 6.2 Hz, 2H), 3.79 (dd, J = 9.0, 5.8 Hz, 2H), 2.98 (s, 3H), 2.90 (s, 3H), 2.89 (s, 6H). 131 1H NMR (400 MHz, DMSO-d6) 10.11 (s, 1H), 8.04 (s, 1H), 7.90 (d, J = 8.6 Hz, 1H), 7.71 (d, J = 7.6 Hz, 1H), 7.67- 7.52 (m, 2H), 7.45 (dd, J = 7.6 Hz, 1H), 7.40-7.29 (m, 3H), 7.27 (d, J = 8.6 Hz, 1H), 7.14 (dd, J = 8.0 Hz, 1H), 7.06 (d, J = 8.0 Hz, 1H), 6.79 (d, J = 7.7 Hz, 1H), 6.77-6.66 (m, 2H), 3.95 (s, 3H), 3.88-3.65 (m, 4H), 2.98 (s, 3H), 2.90 (s, 3H), 2.87 (s, 6H). 132 .sup.1H NMR (400 MHz, Chloroform-d) 8.05 (d, J = 2.0 Hz, 1H), 7.74 (s, 1H), 7.64 (dd, J = 8.6, 2.0 Hz, 1H), 7.55-7.47 (m, 2H), 7.39 (dd, J = 7.5 Hz, 1H), 7.36-7.23 (m, 5H), 7.18-7.10 (m, 2H), 7.08-7.02 (m, 2H), 7.00 (d, J = 8.7 Hz, 1H), 6.81 (brd, J = 6.4 Hz, 1H), 3.88 (s, 3H), 3.74 (t, J = 5.8 Hz, 2H), 3.65 (t, J = 5.8 Hz, 2H), 3.11 (s, 3H), 2.97 (s, 3H), 2.16 (p, J = 5.8 Hz, 2H). 133 1H NMR (400 MHz, Chloroform-d) 8.04 (d, J = 2.4 Hz, 1H), 7.67 (ddd, J = 8.6, 2.2 Hz, 1H), 7.55-7.49 (m, 2H), 7.38 (dd, J = 8.0 Hz, 1H), 7.35-7.31 (m, 1H), 7.20-7.06 (m, 5H), 7.03 (dd, J = 8.7, 2.8 Hz, 1H), 6.98 (d, J = 8.4 Hz, 1H), 6.90 (dd, J = 7.5 Hz, 1H), 6.84-6.77 (m, 1H), 3.98 (s, 3H), 3.93 (brs, 1H), 3.78 (brs, 1H), 3.66 (brs, 1H), 3.34 (brs, 1H), 3.11 (s, 3H), 2.97 (s, 3H), 2.76 (s, 6H), 2.18 (brs, 1H), 1.68 (brs, 1H). 134 .sup.1H NMR (400 MHz, Chloroform-d) 8.05 (d, J = 2.3 Hz, 1H), 7.68 (ddd, J = 8.7, 1.7 Hz, 1H), 7.58-7.51 (m, 2H), 7.40 (dd, J = 7.9 Hz, 1H), 7.34 (d, J = 7.6 Hz, 1H), 7.19 (dd, J = 8.0 Hz, 2H), 7.15-7.01 (m, 4H), 6.88-6.79 (m, 1H), 6.69 (brs, 1H), 6.63 (brd, J = 7.7 Hz, 1H), 6.59 (brd, J = 8.0 Hz, 1H), 4.00 (s, 3H), 3.75 (t, J = 5.9 Hz, 2H), 3.70 (t, J = 5.1 Hz, 2H), 3.12 (s, 3H), 2.98 (s, 3H), 2.91 (s, 6H), 2.19 (p, J = 5.5 Hz, 2H). 135 1H NMR (400 MHz, Chloroform-d) 8.04 (d, J = 2.3 Hz, 1H), 7.69 (dd, J = 8.6, 2.4 Hz, 1H), 7.56-7.50 (m, 2H), 7.40 (dd, J = 7.3 Hz, 1H), 7.33 (ddd, J = 7.7, 1.3 Hz, 1H), 7.15-7.03 (m, 6H), 6.96-6.88 (m, 1H), 6.82 (ddd, J = 6.5, 2.1 Hz, 1H), 6.68 (d, J = 8.9 Hz, 2H), 4.03 (s, 3H), 3.72 (brd, J = 6.7 Hz, 2H), 3.68 (brd, J = 6.2 Hz, 2H), 3.11 (s, 3H), 2.98 (s, 3H), 2.91 (s, 6H), 2.17 (p, J = 5.9 Hz, 2H). 136 1H NMR (400 MHz, Chloroform-d) 8.04 (d, J = 2.1 Hz, 1H), 7.69 (d, J = 8.5 Hz, 1H), 7.52 (brs, 2H), 7.40 (dd, J = 7.8 Hz, 1H), 7.33 (d, J = 7.2 Hz, 1H), 7.18 (dd, J = 8.0 Hz, 1H), 7.15-6.99 (m, 4H), 6.89 (brs, 1H), 6.80 (brd, J = 7.1 Hz, 1H), 6.65-6.51 (m, 3H), 4.04 (s, 3H), 3.71 (brd, J = 14.9 Hz, 4H), 3.11 (s, 3H), 2.97 (s, 3H), 2.92 (s, 6H), 1.79 (brs, 4H).

Experimental Example 1

(421) Evaluation of Agonist Activity Against OX1R and OX2R

(422) NAFT-luciferase gene and human OX1R gene were constitutively expressed in CHO cell, which is a cell line derived from Chinese hamster ovary to establish a cell line (CHOOX1R) and NAFT-luciferase gene and human OX2R gene were constitutively expressed in CHO cell to establish a cell line (CHOOX2R). The respective cells were seeded in a 96-well Multiplate at 10,000 cells/well and cultured in a 5% FBS (Thermo Scientific)-added DMEM medium (Sigma-Aldrich) for 48 hr. The medium was removed, an assay buffer (20 mM HEPES (Sigma-Aldrich), Hanks' balanced salt solution (Gibco), 0.1% BSA (Sigma-Aldrich), 2.5 mM probenecid acid (Wako Pure Chemical Industries, Ltd.)) (100 L) containing 5 M Fura-2AM (Cayman Chemical) was added, and the cells were incubated for 60 min. The buffer containing Fura-2AM was removed, and an assay buffer (75 L) was added. An assay buffer (25 L) containing a test compound was added thereto to start the reaction. Changes in the intracellular calcium ion concentration due to the reaction were measured by measuring the fluorescence intensity ratio by dual wavelength excitation at 340 and 380 nm, by using FDSS7000 (Hamamatsu Photonics K.K.). The test compound was dissolved in DMSO to 10 mM, and diluted with the assay buffer to a final concentration of 10.sup.7M to 10.sup.5M (final concentration of DMSO 1%). The agonist activity values of the respective compounds are shown in Table 21-Table 27.

(423) TABLE-US-00021 TABLE 21 Ex. Response (%) No. concentration OX1R OX2R 1 0.1 M <5 <5 1.0 M <5 6 10 M <5 67 2 0.1 M 13 <5 1.0 M 11 26 10 M 32 74 3 0.1 M 14 <5 1.0 M 9 6 10 M 12 23 4 0.1 M 10 <5 1.0 M 8 <5 10 M <5 16 5 0.1 M 8 10 1.0 M 8 8 10 M 7 19 6 0.1 M 7 9 1.0 M 7 17 10 M 6 32 7 0.1 M 6 8 1.0 M 8 10 10 M 27 24 8 0.1 M 9 8 1.0 M 8 13 10 M 27 61 9 0.1 M 5 <5 1.0 M 6 41 10 M 5 47 10 0.1 M 5 14 1.0 M 6 80 10 M 11 98 11 0.1 M <5 <5 1.0 M <5 <5 10 M 8 9 12 0.1 M <5 <5 1.0 M 11 9 10 M 59 48 13 0.1 M <5 11 1.0 M 63 117 10 M 107 109 14 0.1 M <5 <5 1.0 M <5 18 10 M <5 74 15 0.1 M <5 12 1.0 M <5 81 10 M <5 114 16 0.1 M <5 <5 1.0 M <5 19 10 M 10 82 17 0.1 M <5 <5 1.0 M <5 9 10 M 13 41 18 0.1 M <5 <5 1.0 M <5 6 10 M 15 44 19 0.1 M <5 <5 1.0 M <5 10 10 M <5 58 20 0.1 M <5 <5 1.0 M <5 51 10 M 17 78

(424) TABLE-US-00022 TABLE 22 Response (%) Ex. No. concentration OX1R OX2R 21 0.1 M <5 <5 1.0 M <5 37 10 M 12 54 22 0.1 M <5 57 1.0 M 47 61 10 M 82 48 23 0.1 M <5 54 1.0 M 10 95 10 M 51 86 24 0.1 M <5 <5 1.0 M <5 72 10 M 6 93 25 0.1 M <5 21 1.0 M <5 88 10 M 32 97 26 0.1 M <5 <5 1.0 M <5 51 10 M 9 101 27 0.1 M <5 90 1.0 M 24 126 10 M 70 92 28 0.1 M <5 6 1.0 M <5 54 10 M <5 81 29 0.1 M <5 11 1.0 M <5 84 10 M <5 81 30 0.1 M <5 <5 1.0 M <5 <5 10 M <5 39 31 0.1 M <5 <5 1.0 M <5 10 10 M <5 72 32 0.1 M <5 13 1.0 M <5 79 10 M 14 88 33 0.1 M <5 37 1.0 M <5 92 10 M 50 87 34 0.1 M <5 <5 1.0 M <5 52 10 M <5 95 35 0.1 M <5 <5 1.0 M <5 35 10 M <5 63 36 0.1 M <5 <5 1.0 M <5 63 10 M 10 93 37 0.1 M <5 55 1.0 M <5 88 10 M <5 81 38 0.1 M <5 68 1.0 M <5 82 10 M <5 71 39 0.1 M <5 73 1.0 M <5 59 10 M 32 53 40 0.1 M <5 77 1.0 M <5 60 10 M <5 52

(425) TABLE-US-00023 TABLE 23 Response (%) Ex. No. concentration OX1R OX2R 41 0.1 M <5 17 1.0 M <5 93 10 M <5 102 42 0.1 M <5 93 1.0 M <5 109 10 M <5 95 43 0.1 M <5 102 1.0 M <5 105 10 M 10 104 44 0.1 M <5 100 1.0 M <5 104 10 M 10 95 45 0.1 M <5 82 1.0 M <5 97 10 M <5 100 46 0.1 M <5 74 1.0 M <5 101 10 M 8 115 47 0.1 M <5 7 1.0 M <5 81 10 M <5 102 48 0.1 M <5 <5 1.0 M <5 <5 10 M <5 14 49 0.1 M <5 26 1.0 M <5 89 10 M <5 92 50 0.1 M <5 100 1.0 M <5 94 10 M <5 97 51 0.1 M <5 93 1.0 M 36 85 10 M 67 88 52 0.1 M <5 43 1.0 M <6 81 10 M <7 78 53 0.1 M <8 98 1.0 M 6 95 10 M 26 100 54 0.1 M <5 91 1.0 M <5 71 10 M 10 61 55 0.1 M <5 <5 1.0 M <5 54 10 M <5 105 56 0.1 M <5 95 1.0 M <5 96 10 M 19 82 57 0.1 M <5 91 1.0 M <5 92 10 M <5 60 58 0.1 M <5 <5 1.0 M <5 <5 10 M <5 63 59 0.1 M <5 <5 1.0 M <5 18 10 M <5 52 60 0.1 M <5 <5 1.0 M <5 <5 10 M <5 31

(426) TABLE-US-00024 TABLE 24 Response (%) Ex. No. concentration OX1R OX2R 61 0.1 M <5 24 1.0 M <5 105 10 M 7 99 62 0.1 M 9 6 1.0 M 8 7 10 M 13 9 63 0.1 M 9 8 1.0 M 9 55 10 M 7 66 64 0.1 M <5 <5 1.0 M <5 <5 10 M <5 <5 65 0.1 M <5 <5 1.0 M <5 <5 10 M <5 6 66 0.1 M 6 79 1.0 M 6 70 10 M 7 60 67 0.1 M 6 15 1.0 M 8 83 10 M 9 103 68 0.1 M 6 10 1.0 M 6 10 10 M 6 57 69 0.1 M 6 7 1.0 M 6 90 10 M 6 127 70 0.1 M 6 9 1.0 M 6 9 10 M 6 46 71 0.1 M 6 106 1.0 M <5 97 10 M 10 113 72 0.1 M <5 7 1.0 M <5 59 10 M <5 79 73 0.1 M 6 25 1.0 M 6 49 10 M <5 11 74 0.1 M 6 15 1.0 M 7 13 10 M 7 64 75 0.1 M <5 61 1.0 M <5 94 10 M 30 95 76 0.1 M <5 93 1.0 M 20 90 10 M 55 89 77 0.1 M <5 <5 1.0 M <5 51 10 M <5 99 78 0.1 M <5 23 1.0 M <5 89 10 M 14 86 79 0.1 M <5 <5 1.0 M <5 <5 10 M <5 51 80 0.1 M <5 <5 1.0 M <5 <5 10 M <5 23

(427) TABLE-US-00025 TABLE 25 Response (%) Ex. No. concentration OX1R OX2R 81 0.1 M <5 <5 1.0 M <5 <5 10 M 7 27 82 0.1 M <5 <5 1.0 M <5 <5 10 M 7 16 83 0.1 M <5 <5 1.0 M <5 <5 10 M 9 11 84 0.1 M <5 6 1.0 M <5 6 10 M 10 21 85 0.1 M <5 <5 1.0 M <5 <5 10 M <5 12 86 0.1 M <5 <5 1.0 M <5 <5 10 M <5 11 87 0.1 M <5 <5 1.0 M <5 10 10 M <5 56 88 0.1 M 7 15 1.0 M 7 13 10 M 9 13 89 0.1 M <5 7 1.0 M <5 8 10 M <5 31 90 0.1 M <5 <5 1.0 M <5 56 10 M <5 89 91 0.1 M <5 <5 1.0 M <5 <5 10 M <5 35 92 0.1 M <5 35 1.0 M 6 95 10 M 30 95 93 0.1 M 10 16 1.0 M 9 77 10 M 20 85 94 0.1 M <5 <5 1.0 M <5 <5 10 M <5 46 95 0.1 M <5 <5 1.0 M <5 11 10 M <5 68 96 0.1 M <5 <5 1.0 M <5 <5 10 M <5 67 97 0.1 M <5 25 1.0 M <5 84 10 M 11 108 98 0.1 M 8 13 1.0 M 8 11 10 M 9 67 99 0.1 M 8 19 1.0 M 8 14 10 M 9 76 100 0.1 M <5 <5 1.0 M <5 7 10 M <5 49

(428) TABLE-US-00026 TABLE 26 Response (%) Ex. No. concentration OX1R OX2R 101 0.1 M <5 20 1.0 M <5 89 10 M <5 111 102 0.1 M <5 61 1.0 M <5 97 10 M <5 100 103 0.1 M <5 4 1.0 M <5 27 10 M <5 84 104 0.1 M 7 7 1.0 M 6 79 10 M 7 99 105 0.1 M 8 9 1.0 M 7 32 10 M 8 92 106 0.1 M 8 9 1.0 M 7 7 10 M 8 46 107 0.1 M <5 7 1.0 M <5 9 10 M <5 80 108 0.1 M <5 6 1.0 M <5 6 10 M <5 24 109 0.1 M 8 7 1.0 M 9 6 10 M 7 39 110 0.1 M <5 38 1.0 M <5 86 10 M <5 109 111 0.1 M <5 32 1.0 M <5 88 10 M <5 100 112 0.1 M <5 <5 1.0 M <5 26 10 M <5 69 113 0.1 M <5 <5 1.0 M <5 6 10 M <5 73 114 0.1 M <5 <5 1.0 M <5 <5 10 M <5 28 115 0.1 M <5 <5 1.0 M <5 8 10 M <5 62 116 0.1 M 6 7 1.0 M 9 6 10 M 7 7 117 0.1 M <5 <5 1.0 M <5 16 10 M <5 44 118 0.1 M 9 11 1.0 M 8 36 10 M 9 71 119 0.1 M <5 49 1.0 M <5 85 10 M <5 98 120 0.1 M <5 29 1.0 M <5 84 10 M <5 103

(429) TABLE-US-00027 TABLE 27 Response (%) Ex. No. concentration OX1R OX2R 121 0.1 M <5 7 1.0 M <5 47 10 M 10 104 122 0.1 M <5 7 1.0 M <5 7 10 M <5 10 123 0.1 M <5 63 1.0 M 6 111 10 M <5 111 124 0.1 M 8 9 1.0 M 7 78 10 M 8 147 125 0.1 M <5 42 1.0 M <5 78 10 M <5 79 126 0.1 M 5 7 1.0 M 5 37 10 M <5 85 127 0.1 M <5 106 1.0 M 7 90 10 M 56 73 128 0.1 M <5 10 1.0 M <5 77 10 M 6 105 129 0.1 M <5 85 1.0 M 41 93 10 M 81 92 130 0.1 M <5 64 1.0 M <5 99 10 M 6 106 131 0.1 M <5 43 1.0 M <5 96 10 M 18 101 132 0.1 M <5 42 1.0 M <5 100 10 M 46 101 133 0.1 M 25 107 1.0 M 86 81 10 M 84 72 134 0.1 M 9 101 1.0 M 13 76 10 M 84 75 135 0.1 M 8 94 1.0 M 14 66 10 M 83 64 136 0.1 M <5 144 1.0 M 78 97 10 M 110 94

(430) (As used herein, Response in Table 21 to Table 27 is a value obtained by dividing the agonist activity value, when the test compound is evaluated with orexin-A as a full-agonist (maximum value of agonist activity: 100%), at 10 M, 1.0 M, 0.1 M by the agonist activity value of orexin-A.)

Experimental Example 2

(431) Awakening Effect on Wild-Type Mouse by Light Period Intraventricular Administration of the Compound of the Present Invention

(432) As the experiment animal, C57BL/6 lineage wild-type mouse (male) was used. The mice before and after 9-week-old (1 week) underwent surgery for embedding electroencephalogram electrodes into the skull (Bregma: X=1.5; Y=0.6, Lambda: X=1.5; Y=0) and inserting electromyogram electrodes into the trapezius muscle under isoflurane anesthesia. The mice for intraventricular administration also underwent cannula embedding into lateral cerebral ventricle (Bregma: X=0.9; Y=0.3). From two weeks thereafter, the administration and electroencephalogram measurement were started. The experiment was conducted under a light-dark cycle environment in which the light period started at 9 (ZT0) and the dark period started at 21 (ZT12).

(433) The test compound (compound of Example 40) (10 nmol; dissolved in 5% chromophore-containing saline) (5 l) was injected at ZT6 into the lateral cerebral ventricle of wild-type mice under isoflurane anesthesia through cannula by using a microsyringe pump at a flow rate of 0.5 l/min, and electroencephalogram and electromyogram was measured thereafter. The administration was started with 5% chromophore-containing saline (Vehicle) as a control, and then the test compound was administered. In each case, one day after the administration was set as a recovery period. The results are shown in the FIGURE.

(434) When the test compound was intraventricularly administered in the light period (ZT6), which is a sleep period for mouse, the conscious time increased in the wild-type mouse as compared to the Vehicle administration.

INDUSTRIAL APPLICABILITY

(435) The compound of the present invention shows an orexin receptor agonist activity, and is useful as a prophylactic or therapeutic agent for narcolepsy and the like.

(436) This application is based on a patent application No. 2015-119785 filed in Japan (filing date: Jun. 12, 2015), the entire contents of which are incorporated by reference herein.