Quinolone derivative or pharmaceutically acceptable salt thereof

Information

  • Patent Grant
  • 8133882
  • Patent Number
    8,133,882
  • Date Filed
    Wednesday, March 14, 2007
    17 years ago
  • Date Issued
    Tuesday, March 13, 2012
    12 years ago
Abstract
Provided are quinolone derivatives having a lower alkyl or cycloalkyl at the 1-position; —N(R0)C(O)-lower alkylene-CO2R0, lower alkylene-CO2R0, lower alkenylene-CO2R0, —O-lower alkylene-CO2R0, —O-(lower alkylene which may be substituted with —CO2R0)-aryl or —O-lower alkenylene-CO2R0 (wherein R0 is H or lower alkyl) at the 3-position; halogen at the 6-position; and amino group substituted with a substituent group having a ring structure at the 7-position, respectively, or pharmaceutically acceptable salts thereof. Pharmaceutical composition containing the quinolone derivatives and methods of using the compositions are provided.
Description
TECHNICAL FIELD

The present invention relates to a pharmaceutical, particularly a novel quinolone derivative or a pharmaceutically acceptable salt thereof, which is useful as a platelet aggregation inhibitor or a P2Y12 inhibitor.


BACKGROUND OF THE INVENTION

Since the discovery by Donne et al. in 1842, blood platelets have been regarded for a long time as a component of blood necessary for hemostasis. Nowadays, it has been revealed that platelets not only simply play the leading role in the hemostatic mechanism but also show clinically noteworthy multifunctional properties such as concern in the realization of arteriosclerosis, circulatory organ diseases including thrombotic diseases, metastasis, inflammation, rejection reaction after transplantation and immune reaction.


In general, therapies for blood reperfusion with pharmaceutical agents or physical methods have been carried out for thrombotic diseases and ischemic diseases. However, a phenomenon in which activation, adhesion and aggregation of platelets are accelerated after carrying out revascularization due to breakdown of vascular tissues including endothelial cells, or collapse of fibrinolysis-coagulation balance or the like caused by the drug itself, has recently been found and causing clinical problems. For example, it has been revealed that after recirculation by a thrombolytic therapy using t-PA or the like, fibrinolysis ability and coagulation ability are activated and systemic coagulation-fibrinolysis balance collapses. Clinically, it results in re-obstruction which has been causing a therapeutically large problem (Non-patent reference 1).


On the other hand, a PTCA therapy or a stent indwelling method has been rapidly popularizing and gaining a certain fruit for the treatment of diseases based on angina pectoris, myocardial infarction and the like coronary artery stricture and aorta stricture. However, since these therapeutic methods damage vascular tissues including endothelial cells, acute coronary obstruction, and further re-stricture which occurs at chronic stage, has been causing problems. Platelets are taking an important role in various thrombolytic ill effects (re-obstruction and the like) after such a revascularization. Thus, effectiveness of an anti-platelet agent is expected, but sufficient effects of the conventional anti-platelet agents have not been confirmed.


As preventive or therapeutic agents for such circulatory organ system diseases, aspirin, cilostazol, prostaglandin I2, prostaglandin E1, ticlopidine, clopidogrel, dipyridamole and the like platelet aggregation inhibitors have been used. Also in recent years, a GPIIb/IIIa antagonist which inhibits the final step of platelet aggregation and has strong platelet aggregation inhibition activity has been developed, but its use is limited to the intravenous drip infusion at thrombosis acute phase (Non-patent reference 2).


In recent years, it has been revealed that, regarding ticlopidine and clopidogrel which are used as anti-platelet agents, these are exerting platelet aggregation inhibitory activity through the inhibition of P2Y12 as an ADP receptor by their active metabolites. Thereafter, a triazolo[4,5-D]pyrimidine derivative (Patent reference 1), piperazine and/or homopiperazine derivatives (Patent Reference 2 and Patent Reference 3), a pyrazolidinedione derivative (Patent Reference 4), an isoquinolinone derivative (Patent Reference 5) and the like have been reported as compounds having P2Y12 inhibitory activity.


On the other hand, Patent References 6 and 7 are known as quinolone derivatives.


In Patent Reference 6, a compound represented by a formula (A) having antimicrobial action is known, but possession of platelet aggregation inhibitory activity by these derivatives is not known. In addition, its structure is different from the compound of the present invention in terms that the moiety which corresponds to R5 of the compound of the present invention is a carboxylic acid, ester or carbamoyl.




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(In the formula, R1 represents —OR9, amino group or lower alkylamino group, and R9 hydrogen atom or a carboxy-protecting group. See said official gazette for other symbols.)


In Patent Reference 7, it is reported that a compound represented by a formula (B) has P2Y12 inhibitory activity. However, its structure is different from the compound of the present invention in terms that the moiety which corresponds to R5 of the compound of the present invention is carbamoyl.




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(See Said Official Gazette for Symbols in the Formula.)


In Patent Reference 8, it is reported that a compound represented by a formula (C) has P2Y12 inhibitory activity. However, its structure is different from the compound of the present invention in terms that the moiety which corresponds to R5 of the compound of the present invention is carbamoyl.




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(See Said Official Gazette for Symbols in the Formula.)

  • Non-patent reference 1: “Journal of American College of Cardiology”, 1988, vol. 12, p. 616-623
  • Non-patent reference 2: “Sogo Rinsho (Synthetic Clinic)”, 2003, vol. 52, p. 1516-1521
  • Patent Reference 1: International Publication WO 00/34283
  • Patent Reference 2: International Publication WO 02/098856
  • Patent Reference 3: International Publication WO 03/022214
  • Patent Reference 4: International Publication WO 05/000281
  • Patent Reference 5: International Publication WO 05/035520
  • Patent Reference 6: International Publication WO 98/23592
  • Patent Reference 7: International Publication WO 05/009971
  • Patent Reference 8: International Publication WO 06/077851


DISCLOSURE OF THE INVENTION
Problems that the Invention is to Solve

Under such a situation, it is strongly desired to develop an anti-platelet agent with a high safety profile with a smaller adverse bleeding effect and with distinct pharmaceutical efficacies at not only acute phase but also chronic phase. Thus, it is an object of the invention to develop a platelet aggregation inhibitor or a P2Y12 inhibitor having a high pharmacological effect and a good balance between the pharmacological effect and the safety profile.


Means for Solving the Problems

Accordingly, the present inventors have conducted intensive studies with the aim of overcoming the above-mentioned problems and, as a result, found that a novel quinolone derivative has excellent platelet aggregation inhibitory activity or P2Y12 inhibitory activity and has excellent pharmacokinetics, and thereby accomplished the present invention.


That is, the present invention relates to a quinolone derivative represented by the following general formula (I) or a pharmaceutically acceptable salt thereof




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[Symbols in the formula represent the following meanings,


R1: cycloalkyl or lower alkylene-cycloalkyl,


wherein cycloalkyl in R1 may be substituted,


R2: —H or halogen,


R3: —H, halogen, —OR0 or —O-lower alkylene-aryl,


R0: the same or different from each other and each represents —H or lower alkyl,


R4: lower alkyl, halogeno-lower alkyl, lower alkylene-cycloalkyl, cycloalkyl or heterocyclic group,


wherein cycloalkyl and heterocyclic group in R4 may respectively be substituted,


R5: —NO2, —CN, lower alkyl, lower alkenyl, halogeno-lower alkenyl, -L-Ra, —C(O)R0, —O—Rb, —N(R6)2, lower alkylene-N(R6)(Rc), —N(R6)C(O)—Rd, lower alkylene-N(R6)C(O)—Rd, lower alkylene-N(R0)C(O)O-lower alkyl, —N(R0)C(O)N(R0)—Re, lower alkylene-N(R0)C(O)N(R0)—Re, —N(R0)S(O)2N(R0)C(O)—Rd, —CH═NOH, cycloalkyl, heterocyclic group, (2,4-dioxo-1,3-thiazolidin-5-ylidene)methyl or (4-oxo-2-thioxo-1,3-thiazolidin-5-ylidene)methyl,


wherein cycloalkyl and heterocyclic group in R5 may respectively be substituted,


R6: H, lower alkyl, lower alkylene-CO2R0 or lower alkylene-P(O)(ORp)2,


wherein lower alkylene in R6 may be substituted,


L: lower alkylene or lower alkenylene which may respectively be substituted


Ra: —OR0, —CN, —O-lower alkylene-aryl, —O-lower alkylene-CO2R0, —C(O)R0, —CO2R0, —C(O)NHOH, —C(O)N(R6)2, —C(O)N(R0)-aryl, —C(O)N(R0)—S(O)2-lower alkyl, —C(O)N(R0)—S(O)2-aryl, —C(O)N(R0)—S(O)2-heterocyclic group, —NH2OH, —OC(O)R0, —OC(O)-halogeno-lower alkyl, —P(O)(ORp)2, aryl or heterocyclic group,


wherein aryl and heterocyclic group in Ra may be substituted,


Rp: R0, lower alkylene-OC(O)-lower alkyl, lower alkylene-OC(O)-cycloalkyl, lower alkylene-OC(O)O-lower alkyl, lower alkylene-OC(O)O-cycloalkyl, or lower alkylene-heterocyclic group,


wherein heterocyclic group in Rp may be substituted,


Rb: H, cycloalkyl, aryl, heterocyclic group, lower alkylene-Rba or lower alkenylene-Rba, wherein lower alkylene, lower alkenylene, cycloalkyl, aryl and heterocyclic group in Rb may be substituted,


Rba: —OR0, —O—Si(lower alkyl)3, —CO2R0, —C(O)NHOH, —C(O)N(R0)2, —C(O)N(R0)—S(O)2-lower alkyl, —C(O)N(R0)—S(O)2-aryl, —C(NH2)═NOH, —C(NH2)═NO—C(O)R0, —C(NH2)═NO—C(O)-lower alkylene-C(O)R0, —CO2-lower alkylene-aryl, —P(O)(ORp)2, —C(O)R0, —C(O)-aryl, cycloalkyl, aryl or heterocyclic group,


wherein aryl and heterocyclic group in Rba may be substituted,


Rc: H, lower alkyl, lower alkylene-OR0, lower alkylene-CO2R0, lower alkylene-C(O)NHOH, lower alkylene-C(O)N(R0)2, lower alkylene-P(O)(ORp)2, lower alkylene-aryl, lower alkylene-heterocyclic group, aryl or heterocyclic group,


wherein lower alkylene, aryl and heterocyclic group in Rc may be substituted,


Rd: C1-7 alkyl, lower alkenyl, halogeno-lower alkyl, lower alkylene-Rda, lower alkenylene-Rda, cycloalkyl, aryl or heterocyclic group,


wherein lower alkylene, lower alkenylene, cycloalkyl, aryl and heterocyclic group in Rd may be substituted,


Rda: —CN, —OR0, —OC(O)R0, —O-lower alkylene-CO2R0, —O-aryl, —CO2R0, —C(O)NHOH, —C(O)N(R0)2, —CO2-lower alkylene-N(R0)2, —P(O)(ORp)2, —N(R6)2, —N(R0)C(O)R0, —C(O)N(R0)-aryl, —C(O)N(R0)-(lower alkylene which may be substituted with —CO2R0)-aryl, —N(R0)C(O)-aryl, —N(R0)C(O)—OR0, —N(R0)C(O)—O-lower alkylene-aryl, —N(R0)S(O)2-aryl, —S-heterocyclic group, —C(O)N(R0)-heterocyclic group, —N(R0)C(O)-heterocyclic group, cycloalkyl, aryl or heterocyclic group,


wherein cycloalkyl, aryl and heterocyclic group in Rda may be substituted,


Re: lower alkylene-CO2R0, lower alkylene-C(O)NHOH, lower alkylene-C(O)N(R0)2, lower alkylene-heterocyclic group, aryl, heterocyclic group, —S(O)2-aryl or —S(O)2-heterocyclic group,


wherein aryl and heterocyclic group in Re may be substituted,


X: CH or N,


A: C(R7) or N,


R7: —H and lower alkyl,


or R4 and R7 may together form lower alkylene which may be substituted, with the proviso that


7-(cyclohexylamino)-1-ethyl-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carbonitrile is excluded. The same shall apply hereinafter.]


In addition, this application relates to a pharmaceutical, particularly a P2Y12 receptor inhibitor and/or a platelet aggregation inhibitor, which comprises a quinolone derivative represented by the general formula (I) or a salt thereof as the active ingredient.


Further, this application also relates to the use of a compound represented by the formula (I) or a pharmaceutically acceptable salt thereof for the manufacture of a P2Y12 receptor inhibitor and/or a platelet aggregation inhibitor, and to a method for treating a circulatory organ system disease closely related to the thrombus formation by platelet aggregation, which comprises administering an effective amount of a compound represented by the formula (I) or a pharmaceutically acceptable salt thereof to a patient. That is, (1) a pharmaceutical composition which comprises a compound described in the general formula (I) or a pharmaceutically acceptable salt thereof and a pharmaceutically acceptable carrier.


(2) The pharmaceutical composition of (1) which is a platelet aggregation inhibitor.


(3) The pharmaceutical composition of (1) which is a P2Y12 inhibitor.


(4) Use of a compound described in the general formula (I) or a pharmaceutically acceptable salt thereof for the manufacture of a platelet aggregation inhibitor or a P2Y12 inhibitor.


Effect of the Invention

Since the compound of the present invention has excellent platelet aggregation inhibitory activity or P2Y12 inhibitory activity, it is useful as a pharmaceutical, particularly a platelet aggregation inhibitor or a P2Y12 inhibitor. Accordingly, the compound of the present invention is useful as a preventive and/or therapeutic agent for a circulatory organ system disease closely related to the thrombus formation by platelet aggregation, such as unstable angina, acute myocardial infarction and its secondary prevention, re-obstruction and re-stricture after hepatic coronary artery bypass surgery, PTCA operation or stent indwelling operation, hepatic coronary artery thrombolysis acceleration and re-obstruction prevention and the like ischemic diseases; transient cerebral ischemic attack (TIA) cerebral infarction, subarachnoid hemorrhage (vasospasm) and the like cerebrovascular accidents; chronic arterial occlusive disease and the like peripheral arterial diseases; and the like, and as an auxiliary agent at the time of cardiac surgical operation or vascular surgical operation.







BEST MODE FOR CARRYING OUT THE INVENTION

The following describes the present invention further in detail.


In this description, the “lower alkyl”, “lower alkenyl”, “lower alkylene” and “lower alkenylene” respectively mean hydrocarbon chains having from 1 to 6 carbon atoms which maybe in the straight chain or branched chain form, unless otherwise noted.


Accordingly, the “lower alkyl” means a C1-6 alkyl, and illustrative examples thereof include methyl, ethyl, propyl, butyl, pentyl or hexyl, or structures isomers thereof such as isopropyl, tert-butyl or the like, preferably a C1-5 alkyl, more preferably methyl, ethyl, propyl, isopropyl, butyl, isobutyl, tert-butyl or 3-pentyl.


The “lower alkenyl” means a C2-6 alkenyl, and it may have two or more double bonds. Illustrative examples thereof include ethenyl, propenyl, butenyl, pentenyl, hexenyl, butadienyl and the like, of which preferred is a C2-3 alkenyl and more preferred is ethenyl or propenyl.


The “lower alkylene” means a divalent group in which one hydrogen is removed from an optional position of the “lower alkyl”, and is illustratively methylene, methylmethylene, ethylene, propylene, butylene or the like, preferably a C1-4 alkylene, more preferably methylene, methylmethylene, ethylene or propylene.


The “lower alkenylene” means a divalent group in which one hydrogen is removed from an optional position of the “lower alkenyl”, and is illustratively vinylene, propenylene, butenylene or the like, preferably a C2-3 alkenylene, more preferably vinylene, propenylene.


The “halogen” means a monovalent group of halogen atom, and fluoro, chloro, bromo, iodo or the like may be cited illustratively, of which fluoro or chloro is preferred.


The “halogeno-lower alkyl” means a group in which at least one optional hydrogen atom of the aforementioned “lower alkyl” is substituted with the aforementioned “halogen”, and illustrative examples thereof include trifluoromethyl, trifluoroethyl or the like, of which trifluoromethyl is preferred.


The “halogeno lower alkenyl” means a group in which at least one optional hydrogen atom of the aforementioned “lower alkenyl” is substituted with the aforementioned “halogen”, and illustrative examples thereof include fluorovinyl, chlorovinyl or the like.


The “cycloalkyl” means a C3-10 non-aromatic hydrocarbon ring, and it may form a bridged ring or a spiro ring, partially have an unsaturated bond or be condensed with benzene ring. However, when benzene ring is condensed, the linking hand is present on the non-aromatic ring. Illustrative examples thereof include cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cyclooctyl, cyclohexenyl, cyclooctdieneyl, adamantly, norbornyl, indanyl having a linking hand at from the 1- to 3-position and the like. Preferred is cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl and more preferred is cyclopentyl or cyclohexyl.


The “aryl” means a monocyclic to tricyclic C6-14 aromatic hydrocarbon ring, and illustrative examples thereof include phenyl, naphthyl or the like, of which phenyl is preferred. In addition, a C5-8 cycloalkyl ring may be condensed. However, when a cycloalkyl ring is condensed, the linking hand is present on the aromatic ring. For example, it may form indanyl having a linking hand at from the 4- to 7-positions, or tetrahydronaphthyl having a linking hand at from the 5- to 8-positions.


The “hetero ring” is a general name which includes “aromatic hetero ring” and “non-aromatic hetero ring”. The “aromatic hetero ring” means a monocyclic aromatic hetero ring which is a monocyclic 5- to 7-membered aromatic group containing from 1 to 4 of the same or different hetero atoms selected from the group consisting of nitrogen, oxygen and sulfur, a bicyclic aromatic hetero ring in which monocyclic aromatic hetero rings are condensed or a monocyclic aromatic hetero ring is condensed with benzene ring, or a tricyclic aromatic hetero ring in which a bicyclic aromatic hetero ring is condensed with a monocyclic aromatic hetero ring or benzene ring. Illustrative examples thereof include pyrrolyl, furyl, thienyl, imidazolyl, pyrazolyl, triazolyl, oxazolyl, thiazolyl, furazanyl, pyridyl, pyranyl, thiopyranyl, pyridazinyl, pyrimidinyl, pyrazyl, indolyl, isoindolyl, indolizinyl, benzofuryl, benzothienyl, benzoimidazolyl, indazolyl, benzotriazolyl, benzoxazolyl, benzothiazolyl, benzoxadiazonyl, quinolyl, isoquinolyl, chromenyl, benzothiopyranyl, phthalazinyl, naphthyridinyl, quinoxalinyl, quinazolinyl, cinnolinyl, benzodioxolyl, benzodioxinyl, benzodioxepinyl, carbazolyl and the like, and the nitrogen atom and/or sulfur atom constituting these rings may be oxidized. In addition, these rings may be partially saturated. Preferred is pyridyl, furyl, thienyl, indolyl or quinolyl.


The “non-aromatic hetero ring” means a saturated or partially saturated monocyclic 3- to 10-membered, preferably 5- to 7-membered, monocyclic non-aromatic hetero ring which contains from 1 to 4 hetero atoms selected from O, S and N, a bicyclic non-aromatic hetero ring in which monocyclic non-aromatic hetero rings are ring-condensed or a monocyclic non-aromatic hetero ring is ring-condensed with a monocyclic non-aromatic hetero ring, a C5-8 cycloalkyl ring, benzene ring or an aromatic hero ring, or a tricyclic non-aromatic hetero ring in which a bicyclic non-aromatic hetero ring is ring-condensed with a C5-8 cycloalkyl ring, benzene ring or an aromatic hero ring. These may form oxide or dioxide trough the oxidation of the S or N as the ring atom or may form a bridged ring or a spiro ring. Illustrative examples thereof include hydropyridyl, dihydropyrrolyl, dihydrooxazolyl, dihydrothiazolyl, dihydroimidazolyl, piperidyl, morpholinyl, thiomorpholinyl, piperazinyl, pyrazolidinyl, imidazolidinyl, pyrrolidinyl, oxazolidinyl, thiazolidinyl, azepanyl, homopiperazinyl, tetrahydrofuranyl, tetrahydropyranyl, tetrahydropyrimidinyl, chromanyl, dioxoranyl, homomorpholinyl and the like. Preferred is pyrrolidinyl, piperidinyl, morpholinyl, thiomorpholinyl or piperazinyl.


The term “may be substituted” means “not substituted” or “substituted with the same or different 1 to 5 substituent groups”.


In the specification, the substituents acceptable as those for the phrase “which may be substituted” satisfactorily include those for routine use in the art as substituents for the individual groups. In addition, when two or more groups are present like the case of the R0 of —N(R0)2, respective groups may be the same or different from each other.


As the acceptable substituent group of the “lower alkylene” which may be substituted in R6, halogen may preferably be cited.


Preferably, a group selected from the following group G1 may be cited as the acceptable substituent group of the “lower alkylene” and “lower alkenylene” which may be substituted in L; the “lower alkylene” and “lower alkenylene” which may be substituted in Rb; the “lower alkylene” which may be substituted in Rc; the “lower alkylene” and “lower alkenylene” which may be substituted in Rd; and the “lower alkylene”, formed by R4 and R7, which may be substituted.


Group G1: halogen, —OR0, —CO2R0 and —CO2-lower alkylene-aryl.


Preferably, a group selected from the following group G2 may be cited as the acceptable substituent group of the “cycloalkyl” which may be substituted in R1; the “cycloalkyl” which may be substituted in R4; the “cycloalkyl” which may be substituted in R5; the “cycloalkyl” which may be substituted in Rb; the “cycloalkyl”, which may be substituted in Rd; and the “cycloalkyl”, which may be substituted in Rda.


Group G2: halogen, lower alkyl, —OR0, —CO2R0 and —C(O)-aryl.


Preferably, a group selected from the following group G3 may be cited as the acceptable substituent group of the “aryl” which may be substituted in Ra; the “aryl” which may be substituted in Rb; the “aryl” which may be substituted in Rba; the “aryl” which may be substituted in Rc; the “aryl” which may be substituted in Rda; and the “aryl” which may be substituted in Re.


Group G3: halogen, —CN, lower alkyl, halogeno-lower alkyl, —OR0, —O-halogeno-lower alkyl, —CO2R0 and —O-lower alkylene-CO2R0.


Preferably, a group selected from the following group G4 may be cited as the acceptable substituent group of the “aryl” which may be substituted in Rd.


Group G4: halogen, —CN, —NO2, lower alkyl, halogeno-lower alkyl, —OR0, —O-halogeno-lower alkyl, —C(O)R0, —CO2R0, lower alkylene-CO2R0, —O-lower alkylene-CO2R0, —OC(O)R0, —N(R0)2, —S(O)2-lower alkyl, aryl and heterocyclic group.


However, the aryl and heterocyclic group in group G4 may be substituted with a group selected from a group Q.


Group Q: halogen, lower alkyl, halogeno-lower alkyl, —OR0, —O-halogeno-lower alkyl, oxo and —CO2R0.


Preferably, a group selected from the following group G5 may be cited as the acceptable substituent group of the “heterocyclic group” which may be substituted in R4; the “heterocyclic group” which may be substituted in R5; the “heterocyclic group” which may be substituted in Ra; the “heterocyclic group which may be substituted in Rb; the “heterocyclic group” which may be substituted in Rp; the “heterocyclic group” which may be substituted in Rba; and the “heterocyclic group” which may be substituted in Re.


Group G5: halogen, lower alkyl, halogeno-lower alkyl, —OR0, —O-halogeno-lower alkyl, oxo, —CO2R0, lower alkylene-C(O)R0, lower alkylene-CO2R0 and —S(O)2-lower alkyl.


Preferably, a group selected from the following group G6 may be cited as the acceptable substituent group of the “heterocyclic group” which may be substituted in Rc; and the “heterocyclic group” which may be substituted in Rda.


Group G6: halogen, lower alkyl, halogeno-lower alkyl, —OR0, —O-halogeno-lower alkyl, oxo, —CO2R0, lower alkylene-C(O)2R0, —S(O)2-lower alkyl, aryl, —S-lower alkylene-aryl and heterocyclic group.


In this regard, the aryl and heterocyclic group in group G6 may be substituted with a group selected from the aforementioned group Q.


Preferably, a group selected from the following group G7 may be cited as the acceptable substituent group of the “heterocyclic group” which may be substituted in Rd.


Group G7: halogen, nitro, lower alkyl, halogeno-lower alkyl, —OR0, —O-halogeno-lower alkyl, oxo, —CO2R0, lower alkylene-CO2R0, —N(R0)2, —S(O)2-lower alkyl, —S(O)2-aryl, aryl, lower alkylene-aryl, heterocyclic group, lower alkylene-heterocyclic group and —S-lower alkylene-CO2R0.


In this regard, the aryl and heterocyclic group in group G7 may be substituted with a group selected from the aforementioned group Q.


A preferred embodiment in the present invention is shown in the following.


(a) Preferred as R1 is cyclohexyl or cyclopropylmethyl, more preferably cyclohexyl.


(b) Preferred as R2 is —F.


(c) Preferred as R3 is —H, —OH or —F, more preferred is —H.


(d) Preferred as R4 is lower alkyl or cycloalkyl, more preferably isopropyl, 3-pentyl or cyclopentyl, further preferred is isopropyl, 3-penthyl or cyclopentyl.


(e) Preferred as R5 is —N(R0)C(O)-lower alkylene-CO2R0, —N(R0)C(O)-lower alkenylene-CO2R0, lower alkylene-CO2R0, lower alkenylene-CO2R0, —O-lower alkenylene-CO2R0, —O-(lower alkylene which may be substituted with —CO2R0)-aryl, —O-lower alkenylene-CO2R0, —O-(lower alkenylene which may be substituted with —CO2R0)-aryl or —O-lower alkenylene-tetrazolyl, more preferably —N(R0)C(O)-lower alkylene-CO2R0, lower alkylene-CO2R0, lower alkenylene-CO2R0, —O-lower alkylene-CO2R0, —O-(lower alkylene which may be substituted with —CO2R0)-aryl or —O-lower alkenylene-CO2R0, further preferably lower alkenylene-CO2R0 or —O-lower alkylene-CO2R0.


(f) Preferred as X is CH.


(g) Preferred as A is CH.


Further, a compound consisting of a combination of the preferred groups of the above-mentioned (a) to (g) is more preferable.


Also, another preferred embodiment of the compound of the present invention represented by the general formula (I) is shown in the following.


(1) The compound described in the general formula (I), wherein X is CH.


(2) The compound described in (1), wherein R3 is —H, —OH or —F.


(3) The compound described in (2), wherein A is CH.


(4) The compound described in (3), wherein R1 is cyclohexyl or cyclopropylmethyl.


(5) The compound described in (4), wherein R2 is —F.


(6) The compound described in (5), wherein R4 is lower alkyl or cycloalkyl.


(7) The compound described in (6), wherein R5 is —N(R0)C(O)-lower alkylene-CO2R0, lower alkylene-CO2R0, lower alkenylene-CO2R0, —O-lower alkylene-CO2R0, —O-(lower alkylene which may be substituted with —CO2R0)-aryl or —O-lower alkenylene-CO2R0.


(8) A compound described in the general formula (I), which is selected from the group consisting of




  • 4-{[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]amino}-4-oxobutanoic acid,

  • 5-{[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]amino}-5-oxopentanoic acid,

  • (2E)-3-[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]acrylic acid,

  • (2S)-2-{[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]oxy}-3-phenylpropanoic acid,

  • (2E)-3-[7-(cyclohexylamino)-6-fluoro-1-isopropyl-4-oxo-1,4-dihydroquinolin-3-yl]acrylic acid,

  • (2S)-2-{[7-(cyclohexylamino)-6-fluoro-1-isopropyl-4-oxo-1,4-dihydroquinolin-3-yl]oxy}-3-phenylpropanoic acid,

  • (2S)-2-{[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]oxy}propanoic acid, and

  • (2S)-2-{[7-(cyclohexylamino)-6-fluoro-1-isopropyl-4-oxo-1,4-dihydroquinolin-3-yl]oxy}propanoic acid,


    or a pharmaceutically acceptable salt thereof.



Also, there is a case in which the compounds of the present invention form salts, and such salts are included in the compounds of the present invention as long as they are pharmaceutically acceptable salts. Illustrative examples thereof include acid addition salts with inorganic acids (e.g., hydrochloric acid, hydrobromic acid, hydriodic acid, sulfuric acid, nitric acid, phosphoric acid and the like), or organic acids (e.g., formic acid, acetic acid, propionic acid, oxalic acid, malonic acid, succinic acid, fumaric acid, maleic acid, lactic acid, malic acid, tartaric acid, citric acid, methanesulfonic acid, ethanesulfonic acid, p-toluenesulfonic acid, aspartic acid, glutamic acid and the like), salts with inorganic bases including metals (e.g., sodium, potassium, calcium, magnesium and the like) or with organic bases (e.g., methylamine, ethylamine, ethanolamine, lysine, ornithine and the like), ammonium salts and the like.


In addition, the compounds of the present invention may have an asymmetric carbon atom in some cases depending on the kind of substituent groups, and optical isomers based on this may be present. The present invention includes all of the mixtures and isolated forms of these optical isomers. Also, tautomers are present in the compounds of the present invention in some cases, and the present invention includes separated forms of these isomers or mixtures thereof. In addition, a labeled substance, namely a compound in which at least one atom of the compound of the present invention is replaced by a radioisotope or non-radioactive isotope, is also included in the present invention.


In addition, various types of hydrate and solvate and polymorphism of the compound of the present invention or a pharmaceutically acceptable salt thereof are also included. In this connection, as a matter of course, the compounds of the present invention are not limited to the compounds described in the Examples which are described later, and all of the derivatives represented by the formula (I) and pharmaceutically acceptable salts thereof are included therein.


In this connection, all of the compounds which are converted in the living body into the compounds of the present invention represented by the aforementioned general formula (I), so-called prodrugs, are also included in the compounds of the present invention. As the groups which can form prodrugs of the compounds of the present invention, the groups described in Prog. Med., 5: 2157-2161 (1985), and the groups described in “Iyakuhin no Kaihatsu (Development of Medicines)”, vol. 7 Bunshi Sekkei (Molecular Design), pp. 163-198, published by Hirokawa Shoten in 1990, may be exemplified.


(Step A)


This step is a step in which a compound (I-a) of the present invention is produced by reducing a compound (1).


As the reduction reaction of this step, a carboxylic acid or ester reduction reaction generally used by those skilled in the art may be employed. For example, this may be carried out under cooling to heating reflux using equimolar to excess amount of a reducing agent such as lithium aluminum hydride, diisobutylaluminum hydride, sodium borohydride or the like, in a reaction inert solvent, for example aromatic hydrocarbons such as benzene, toluene, xylene, ethers such as diethyl ether, tetrahydrofuran (THF), dioxane, halogenated hydrocarbons such as dichloromethane, 1,2-dichloroethane, chloroform, N,N-dimethylformamide (DMF), N,N-dimethylacetamide (DMA), N-methylpyrrolidone (NMP), dimethyl sulfoxide (DMSO), acetonitrile, alcohols such as methanol, ethanol, and water. In addition, when the compound (1) is a carboxylic acid wherein R0 is —H, the carboxylic acid may also be reduced after converting it into a reactive derivative. As the reactive derivative of carboxylic acid, an acylimidazole obtained by reaction with 1,1′-carbonyldiimidazole (CDI), a mixed acid anhydride obtained by reaction with isobutyl chloroformate, etc., and the like may be cited.


(Step B)


This step is a step in which a compound (I-b) of the present invention is produced by oxidizing the compound (I-a) of the present invention.


In the oxidation reaction of this step, an alcohol oxidation reaction generally used by those skilled in the art may be used. For example, this may be carried out under room temperature to heating using equivalent to excess amount of manganese dioxide as an oxidizing agent, in a solvent such as the aforementioned aromatic hydrocarbons, halogenated hydrocarbons or the like.


(Step C)


This step is a step in which a compound (I-c) of the present invention is produced by subjecting the compound (I-b) of the present invention to an oxidation rearrangement reaction (Baeyer-Villiger) and then to hydrolysis.


The oxidation rearrangement reaction of this step may be carried out under room temperature to heating using equivalent to excess amount of m-chloroperbenzoic acid, peracetic acid, aqueous hydrogen peroxide or the like as the oxidizing agent, in a reaction inert solvent such as the aforementioned aromatic hydrocarbons, halogenated hydrocarbons, acetic acid, water or the like.


The hydrolysis reaction of this step may be carried out using an ester hydrolysis reaction generally used by those skilled in the art. For example, it may be carried out under cooling to heating in a reaction inert solvent such as the aforementioned aromatic hydrocarbons, ethers, halogenated hydrocarbons, alcohols, DMF, DMA, NMP, DMSO, pyridine, water or the like in the presence of mineral acid such as sulfuric acid, hydrochloric acid, hydrobromic acid or the like or organic acid such as formic acid, acetic acid or the like, or in the presence of a base such as lithium hydroxide, sodium hydroxide, potassium hydroxide, potassium carbonate, sodium carbonate, cesium carbonate or ammonia or the like.


Depending on the kind of the compounds, the compound (I-c) may be obtained in some cases by advancing to the hydrolysis at a stroke in the oxidation rearrangement reaction.


(Step D)


This step is a step in which a compound (I-d) of the present invention is produced by subjecting the compound (I-c) of the present invention to a nucleophilic substitution reaction.


The nucleophilic substitution reaction of this step may be carried out using an equivalent to excess amount of a compound (2), under room temperature to heating in a solvent such as the aforementioned aromatic hydrocarbons, ethers, halogenated hydrocarbons, DMF, DMA, NMP, DMSO or the like, in the presence of a base such as potassium carbonate, tert-butoxy potassium, sodium hydride, triethylamine or the like.


Second Production Method




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(In the formulae, R10 and R11 mean —H, halogen, —CO2R0 or lower alkyl or aryl which may respectively be substituted, and R20 mean a residual part of the Horner-Emmons reagent (4), R21 mean a residual part of the phosphonium salt (5), Xa− mean Cl, Br or the like counter anion, and R22 mean a residual part of the ylide compound (6).)


(Step E)


This step is a step in which a compound (I-e) of the present invention is produced by subjecting the compound (I-b) of the present invention to a reductive alkylation reaction.


The reductive alkylation reaction of this step may use a reductive alkylation reaction generally used by those skilled in the art. For example, the method described in “Jikken Kagaku Koza (Experimental Chemistry Course)” edited y The Chemical Society of Japan, Vol. 20 (1992) (Maruzen) or the like may be cited. It is desirable to carry out the reaction under cooling to heating reflux using the reducing agent such as sodium borohydride, sodium triacetoxy borohydride, or the like without solvent or in a reaction inert solvent such as the aforementioned halogenated hydrocarbons, aromatic hydrocarbons, ethers, alcohols, esters including ethyl acetate or the like, acetic acid or the like. Depending on the compounds, it is advantageous in some cases to carry out the reaction in the presence of organic acid such as sulfuric acid, hydrochloric acid, hydrobromic acid or the like mineral acid, formic acid, acetic acid or the like or Lewis acid such as titanium(IV) chloride, tetraisopropyl orthotitanate or the like. In addition, it may also be carried out under room temperature to heating in an atmosphere of hydrogen under ordinary pressure to pressurization using, for example, palladium-carbon, rhodium-carbon, Raney nickel, platinum or the like as the catalyst, in a reaction inert solvent such as the aforementioned aromatic hydrocarbons, esters, ethers, halogenated hydrocarbons, DMF, DMA, NMP, acetonitrile, acetic acid or the like. Depending on the compound, it is advantageous in some case in effecting smooth progress of the reaction to allow it to react with an acid (preferably hydrochloric acid, acetic acid or the like).


(Step F)


This step is a step in which a compound (I-f) of the present invention is produced by subjecting the compound (I-b) of the present invention to the Horner-Emmons or Wittig reaction.


The Horner-Emmons or Wittig reaction of this step may use a method generally used by those skilled in the art. For example, when the Horner-Emmons reagent (4) or phosphonium salt (5) is used, the reaction may be carried out under cooling to heating using potassium carbonate, tert-butoxy potassium, sodium hydride, n-butyl n-butyl lithium or the like alkyl lithium or the like as a base, in a solvent such as the aforementioned aromatic hydrocarbons, ethers, halogenated hydrocarbons, DMF, DMA, NMP, DMSO, acetonitrile or the like. Also, when the ylide compound (6) is used, the reaction may be carried out under cooling to heating in a solvent such as the aforementioned aromatic hydrocarbons, ethers, halogenated hydrocarbons, DMF, DMA, NMP, DMSO, acetonitrile or the like.


(Step G)


This step is a step in which a compound (I-g) of the present invention is produced by reducing the double bond of the compound (I-f) of the present invention.


The reduction reaction of this step may use a method generally used by those skilled in the art. For example, it may also be carried out under room temperature to heating in an atmosphere of hydrogen under ordinary pressure to pressurization using palladium-carbon, Raney nickel, platinum or the like as the catalyst, in a reaction inert solvent such as the aforementioned aromatic hydrocarbons, esters, ethers, halogenated hydrocarbons, DMF, DMA, NMP, acetic acid or the like. Depending on the compound, it is advantageous in some case in effecting smooth progress of the reaction to allow it to react with an acid (preferably hydrochloric acid, acetic acid or the like).


Third Production Method




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(In the formulae, L2 represents a leaving group such as halogen, —O-methanesulfonyl, —O-p-toluenesulfonyl or the like. The same shall apply hereinafter.)


(Step H)


This step is a step in which a compound (I-h) of the present invention is produced by subjecting a compound (7) to a nucleophilic substitution reaction.


The nucleophilic substitution reaction of this step may be carried out using a compound (7) and compound (8) in equimolar amounts, or one of them in an excess amount, under room temperature to heating without solvent or in a solvent such as the aforementioned aromatic hydrocarbons, ethers, halogenated hydrocarbons, DMF, DMSO, esters including ethyl acetate or the like, acetonitrile, alcohols or the like. Depending on the compounds, it is advantageous in some case to carry out in the presence of an organic base (triethylamine, diisopropylethylamine, N-methylmorpholine, pyridine, 4-(N,N-dimethylamino)pyridine or the like is suitably used) or a metal salt base (potassium carbonate, cesium carbonate, sodium hydroxide, potassium hydroxide, sodium hydride, tert-butoxy potassium or the like is suitably used).


(Step I)


This step is a step in which a compound (I-i) of the present invention is produced by reducing the compound (I-h) of the present invention.


The nitro-reducing reaction of this step may use a method generally used by those skilled in the art. For example, it may also be carried out under room temperature to heating in an atmosphere of hydrogen under ordinary pressure to pressurization using palladium-carbon, Raney nickel, platinum or the like as the catalyst, in a reaction inert solvent such as the aforementioned aromatic hydrocarbons, esters, ethers, halogenated hydrocarbons, DMF, DMA, NMP, acetic acid or the like. Depending on the compound, it is advantageous in some case in effecting smooth progress of the reaction to allow it to react with an acid (preferably hydrochloric acid, acetic acid or the like).


Fourth Production Method




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(Step J)


This step is a step in which a compound (I-j) of the present invention is produced by dehydrating a compound (9).


The dehydration reaction of this step may use a method which may be generally used in the amide dehydration reaction by those skilled in the art. For example, it may be carried out under room temperature to heating using diphosphorus pentoxide, phosphorus oxychloride, trifluoroacetic anhydride or the like as a dehydrating agent, without solvent or in a reaction inert solvent such as aromatic hydrocarbons, halogenated hydrocarbons, ethers or the like. However, when trifluoroacetic anhydride is used as the dehydrating agent, the 7-position amino group of quinolone is trifluoroacetylated in some cases depending on the kind of the compound, so that there is a case of requiring hydrolysis for the after-treatment. A method which is generally used in the amide hydrolysis by those skilled in the art may be employed in the hydrolysis.


(Step K)


This step is a step in which a compound (I-k) of the present invention is produced by reducing the compound (I-j) of the present invention.


The nitrile-reducing reaction of this step may also be carried out under room temperature to heating in an atmosphere of hydrogen under ordinary pressure to pressurization using palladium-carbon, Raney nickel, platinum or the like as the catalyst, in a reaction inert solvent such as the aforementioned aromatic hydrocarbons, esters, ethers, halogenated hydrocarbons, DMF, DMA, NMP, acetic acid or the like. Depending on the compound, it is advantageous in some case in effecting smooth progress of the reaction to allow it to react with an acid (preferably hydrochloric acid, acetic acid or the like).


Fifth Production Method




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(In the formulae, J represents single bond or lower alkylene, and R12 is R6 or Rc. The same shall apply hereinafter.)


(Step L)


This step is a step in which a compound (I-m) of the present invention is produced by subjecting the compound (I-l) of the present invention to a nucleophilic substitution reaction or reductive alkylation reaction.


The nucleophilic substitution reaction and reductive alkylation reaction of this step may be carried out respectively in the same manner as in the step D and step E.


(Step M)


This step is a step in which a compound (I-n) of the present invention is produced by subjecting the compound (I-m) of the present invention to a nucleophilic substitution reaction or reductive alkylation reaction.


The nucleophilic substitution reaction and reductive alkylation reaction of this step may be carried out respectively in the same manner as in the step D and step E.


Sixth Production Method




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(Step N)


This step is a step in which a compound (I-p) of the present invention is produced by an amidation reaction of a compound (I-o) of the present invention with a compound (10) or a reactive derivative thereof.


The amidation reaction of this step may use an amidation which may be generally used by those skilled in the art. Particularly, a method which uses condensing agent such as carbonyldiimidazole (CDI), 1-ethyl-3-(dimethylaminopropyl)carbodiimide hydrochloride (WSC.HCl), dicyclohexylcarbodiimide, diphenylphosphoryl azide, diethylphosphoryl cyanide or the like, a method which is carried out by way of a mixed acid anhydride using isobutyl chloroformate, ethyl chloroformate and the like, and a method which is carried out by way of an acid halide using thionyl chloride, phosphorus oxychloride or the like are suitable. The reaction conditions may be optionally selected depending on the reactive derivative and condensing agent to be used, and this is generally carried out under cooling, under cooling to room temperature, or under room temperature to heating in a reaction inert solvent such as halogenated hydrocarbons, aromatic hydrocarbons, ethers, DMF, DMSO or the like. Depending on the reaction, it is advantageous in some case to carry out in the presence of an organic base (triethylamine, diisopropylethylamine, N-methylmorpholine, pyridine, 4-(N,N-dimethylamino)pyridine or the like is suitably used) or a metal salt base (potassium carbonate, cesium carbonate or the like is suitably used).


Seventh Production Method




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(In the formulae, L3 represents a leaving group such as —O-lower alkyl, —O-p-nitrophenyl or the like.)


(Step O)


This step is a step in which a compound (I-r) of the present invention is produced by urea formation of a compound (I-q) of the present invention.


The urea formation reaction may be carried out under room temperature to heating using equivalent amounts of the compound (I-q) and a compound (11), or one f them in an excess amount, in a reaction inert solvent such as aromatic hydrocarbons, halogenated hydrocarbons, ethers, DMF, DMSO or the like. Depending on the reaction, it is advantageous in some case to carry out in the presence of an organic base (triethylamine, diisopropylethylamine, N-methylmorpholine, pyridine, 4-(N,N-dimethylamino)pyridine, 1,8-diazabicyclo[5.4.0]-7-undecene or the like is suitably used) or a metal salt base (potassium carbonate, cesium carbonate or the like is suitably used).


In addition, several compounds represented by the formula (I) may also be produced from the compounds obtained in the above manner by optionally combining steps such as conventionally known alkylation, acylation, substitution reaction, oxidation, reduction, hydrolysis and the like, which may be generally employed by those skilled in the art. Particularly, the compounds (I-a), (I-b), (I-c), (I-h), (I-i) and (I-j) of the present invention are also useful as the synthesis intermediates of the compounds of the present invention.


(Synthesis of Starting Compounds)


The starting compounds to be used in the production of the compound (I) of the present invention may be synthesized using the following methods, conventionally known methods or modified methods thereof


(Starting Material Synthesis 1)




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The compound (1-a) may be produced using the method described in the Patent Reference 7 or a modified method thereof


(Step P)


This step is a step in which the compound (9) is produced by the amidation of the compound (1-a).


Regarding the amidation reaction of this step, it may be produced for example by the method described in the step N.


(Starting Material Synthesis 2)




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(Step Q)


This step is a step in which a compound (14) is produced by a condensation reaction of a compound (12) with an orthoformic ester and subsequent addition elimination reaction by a compound (13).


The condensation reaction of this step by an orthoformic ester may be carried out under room temperature to heating by using a reagent which captures alcohols generated from the orthoformic ester as a solvent such as acetic anhydride, or by using a reagent which captures alcohols generated from the orthoformic ester in a reaction inert solvent such as halogenated hydrocarbons, ethers, aromatic hydrocarbons, DMF, DMSO, esters, acetonitrile or the like.


The addition elimination reaction after the above-mentioned condensation reaction may be carried out under cooling, room temperature or heating in a reaction inert solvent such as alcohols, halogenated hydrocarbons, ethers, aromatic hydrocarbons, DMF, DMSO or the like. In this connection, the reaction may also be carried out using excess amount of the compound (13). Depending on the compounds, it is advantageous in some case to carry out in the presence of an organic base (triethylamine, diisopropylethylamine, N-methylmorpholine, pyridine, 4-(N,N-dimethylamino)pyridine or the like is suitably used) or a metal salt base (potassium carbonate, cesium carbonate, sodium hydroxide, potassium hydroxide, sodium hydride, tert-butoxy potassium or the like is suitably used).


(Step R)


This step is a step in which a compound (7) is produced by an intramolecular cyclization reaction of the amino group of the compound (14).


The intramolecular cyclization reaction of this step may be carried out under cooling, room temperature or heating in a reaction inert solvent such as halogenated hydrocarbons, ethers, aromatic hydrocarbons, DMF, DMSO or the like. Depending on the compounds, it is advantageous in some case to carry out in the presence of an organic base (triethylamine, diisopropylethylamine, N-methylmorpholine, pyridine, 4-(N,N-dimethylamino)pyridine, 1,8-diazabicyclo[5.4.0]-7-undecene or the like is suitably used) or a metal salt base (potassium carbonate, cesium carbonate, sodium hydroxide, potassium hydroxide, sodium hydride, tert-butoxy potassium or the like is suitably used).


The compound of the present invention produced in this manner is isolated and purified directly as free or as a salt thereof by applying a salt formation treatment in the usual way. The isolation and purification are carried out by employing general chemical operations such as extraction, concentration, evaporation, crystallization, filtration, recrystallization, various types of chromatography and the like.


Various types of isomers may be isolated in the usual way making use of the difference in the physicochemical properties between isomers. For example, a racemic mixture may be converted into an optically pure isomer by a general racemic resolution method including for example converting to diastereomer salts with optically active acid such as a tartaric acid and subsequent optical resolution. Also, a diastereomer mixture may be separated, for example, by a fractional recrystallization or various types of chromatography. In addition, an optically active compound may also be produced using an appropriate optically active compound as the starting material.


The pharmaceutical composition which contains one or more of the compounds of the present invention or pharmaceutically acceptable salts thereof as the active ingredient is prepared using carriers and fillers and other additive agents generally used in preparing pharmaceuticals.


Its administration may be in the form of either oral administration by tablets, pills, capsules, granules, powders, solutions and the like, or parenteral administration by intravenous, intramuscular or the like injections, suppositories, percutaneous preparations, transnasal preparations, inhalations and the like. Its dose is optionally decided by taking into consideration symptom, age, sex and the like of the object to be treated in response to each case, but in the case of oral administration, it is generally approximately from 0.001 mg/kg to 100 mg/kg per day per adult, and this is administered in one portion or by dividing into 2 to 4 portions. Also, in the case of intravenous administration, it is administered within the range of from 0.0001 mg/kg to 10 mg/kg per adult, once or two or more times per day. In addition, in the case of transnasal administration, it is administered within the range of from 0.0001 mg/kg to 10 mg/kg per adult, once or two or more times per day.


As the solid composition for oral administration by the present invention, tablets, powders, granules and the like are used. In such a solid composition, one or more active substances are mixed with at least one inert diluent such as lactose, mannitol, glucose, hydroxypropylcellulose, microcrystalline cellulose, starch, polyvinyl pyrrolidone, aluminum magnesium silicate or the like. In accordance with the usual way, the composition may contain additive agents other than the inert diluent, such as lubricant (e.g., magnesium stearate or the like), disintegrating agent (e.g., calcium cellulose glycolate or the like), a stabilizing agent, solubilizing agent and the like. When necessary, tablets or pills may be coated with a sugar coating or film of a gastric or enteric substance, such as of sucrose, gelatin, hydroxypropylcellulose, hydroxypropylmethylcellulose phthalate or the like.


The liquid composition for oral administration includes pharmaceutically acceptable emulsions, solutions, suspensions, syrups, elixirs and the like and contains a generally used inert diluent such as purified water or ethanol EtOH). In addition to the inert diluent, this composition may contain a moistening agent, a suspending agent and the like auxiliary agents, as well as sweeteners, flavors, aromatics and antiseptics.


As the injections for parenteral administration, aseptic aqueous or non-aqueous solutions, suspensions and emulsions are included. As the aqueous solutions and suspensions, for example, distilled water for injection and physiological saline are included. As the non-aqueous solutions and suspensions, for example, there are propylene glycol, polyethylene glycol, olive oil or the like plant oil, EtOH or the like alcohols, polysorbate 80 and the like. Such a composition may further contain auxiliary agents such as an antiseptic, a moistening agent, an emulsifying agent, a dispersing agent, a stabilizing agent, a solubilizing agent or the like. These are sterilized for example by filtration through a bacteria retaining filter, blending of a germicide or irradiation. These may also be used by producing sterile solid compositions and dissolving them in sterile water or a sterile solvent for injection prior to their use.


Pharmacological activities of the compounds of the present invention were verified by the following tests.


Test Method (1) Human Platelet Aggregation Inhibition Activity Measuring Test


A blood sample was collected from a healthy volunteers (male adult) using a syringe containing 1/10th volume of 3.8% sodium citrate solution and centrifuged at 160×g for 10 minutes, thereby separating platelet rich plasma (PRP) of the supernatant. Remaining blood after the collection of PRP was centrifuged at 1,800×g for 10 minutes to separate platelet poor plasma (PPP). The number of platelets in the PRP was measured by an automatic blood cell counter (MEK-6258, Nihon Kohden Corp.), and then the number of platelets was adjusted to 3×108/ml by adding PPP to PRP and used in the following test. The ADP as an inducer of platelet aggregation was purchased from MC Medical. Platelet aggregation was measured using an aggregometer (MCM Hematracer 212; MC Medical). That is, 80 μl of PRP of 3×108 platelets/ml and 10 μl of a test compound solution or a solvent (10% DMSO or 10% DMSO-9% hydroxypropyl-β-cyclodextrin-4.5% d-mannitol) were incubated at 37° C. for 1 minute, and then 10 μl of ADP (50 μM) was added thereto to induce platelet aggregation, and changes in transmitted light were recorded for 5 minutes. The inhibition ratio was calculated using the area under platelet aggregation curve as an index. The results at 10 μM (final concentration) of compounds of the present invention are shown in Table 1.


In this connection, REx represents reference example number, and Ex Example compound number. In addition, Reference Examples 1 and 2 are the Example compounds described in the aforementioned Patent Reference 7, and were produced in accordance with the method described in said patent reference.


Reference Example 1
Example 467 of Patent Reference 7
4-({[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]carbonyl}amino)butanoic Acid
Reference Example 2
Example 6 of Patent Reference 7
({[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]carbonyl}amino)acetic Acid











TABLE 1







Compound to be tested
Inhibition %









REx 1
64



REx 2
79



Ex 2
93



Ex 76
94



Ex 80
92



Ex 82
89



Ex 87
92



Ex 114
85



Ex 125
91



Ex 146
83



Ex 202
94



Ex 261
97



Ex 271
91



Ex 297
89



Ex 321
93



Ex 354
85



Ex 380
89



Ex 407
84











Test Method (2) Substitution Test for the Binding of Human P2Y12 with 2-methylthio-ADP (2-MeS-ADP)


A C6-15 cell was inoculated into a 10 cm petri dish to a density of to 1×106 cells using DMEM medium and cultured for 1 day, and then 8 μg of a plasmid pEF-BOS-dfhr-human P2Y12 and 0.8 μg of pEF-BOS-neo (Nucleic Acid Res., 18, 5322, 1990) were gene-transferred using a transfection reagent (LipofectAMINE 2000; mfd. by GIBCO BRL).


24 hours after the aforementioned gene transfer operation, the gene-transferred cells were recovered, suspended in DMEM medium supplemented with 0.6 mg/ml of G 418 (mfd. by GIBCO BRL) and then serially diluted and inoculated again in a 10 cm petri dish. The colonies appeared after 2 weeks were individually obtained and used in the following test as P2Y12 protein expression C6-15 cells (WO 02/36631, Mol. Pharmacol., 60, 432, 2001).


After culturing the P2Y12 protein expression C6-15 cells, the cells were recovered. The cells were washed with PBS, and then suspended in 20 mM Tris-HCl (pH 7.4) containing 5 mmol/l of EDTA and a protease inhibitor cocktail set Complete™ (mfd. by Boehringer-Mannheim) and homogenized using Polytron. After carrying out ultracentrifugation, the precipitate was suspended in 50 mM Tris-HCl (pH 7.4) containing 1 mM EDTA, 100 mM NaCl and Complete™, and this was used as a membrane fraction.


A 100 μl portion of the P2Y12 protein expression C6-15 cell membrane fraction (100 μg/ml) obtained in the above was mixed with 1.5 μl of a test compound solution and 50 μl of 0.75 nM [3H]-2-MeS-ADP (80 Ci/mmol, mfd. by Amersham Pharmacia Biotech) or 0.75 nM [33P]-2-MeS-ADP (2100 Ci/mmol, mfd. by Perkin Elmer), incubated at room temperature for 1 hour in 50 mM Tris-HCl (pH 7.4) containing 100 mM NaCl and 50 mM MgCl2, and then recovered on a glass filter using a cell harvester. A microscintillator was added to the glass filter, and the radioactivity was measured using a liquid scintillation counter. Those to which the solvent alone was added and 1.5 μl of 250 μM ADP was added in the aforementioned test at the same time were regarded as total binding and nonspecific binding, and their radioactivity was measured. By regarding the total binding and nonspecific binding as inhibition ratio 0% and 100% respectively, inhibition ratio (%) of each compound to be tested was calculated. The results at 30 nM (final concentration) of compounds of the present invention are shown in Table 2.












TABLE 2







Compound to be tested
Inhibition %









REx 1
76



REx 2
86



Ex 2
89



Ex 80
89



Ex 82
65



Ex 87
87



Ex 114
92



Ex 125
83



Ex 146
92



Ex 196
86



Ex 202
82



Ex 261
67



Ex 271
80



Ex 321
73



Ex 324
92



Ex 380
96



Ex 407
72



Ex 488
35











Test Method (3) Rat Platelet Aggregation Inhibition Test and Measurement of Test Compound Concentration in Plasma


By adding sodium hydroxide aqueous solution to the compound of the present invention, 0.5% methyl cellulose aqueous solution or suspension was prepared. The thus prepared liquid was orally administered using a sonde to a male SD rat (5 to 7 weeks of age) of after 12 hours or more of fasting. After 2 hours of the compound administration, blood was collected using a syringe containing 1/10th volume of 3.8% sodium citrate solution. In the same manner as in Test method (1), PPP and PRP of 3×108 platelets/ml were prepared. A 90 μl portion of the PRP of 3×108 platelets/ml was incubated at 37° C. for 1 minute, and then 10 μl of ADP (50 μM) was added thereto to induce platelet aggregation, and changes in transmitted light were recorded for 5 minutes. The inhibition ratio was calculated using the area under platelet aggregation curve as an index.


The concentration in plasma was measured using the PPP prepared in the above. In order to prepare a standard curve, a PPP of an SD rat to which the compound was not administered was also separated, and those in which the compound of the present invention was serially diluted with this PPP (from 30 μM to 0.0003 μM in final concentration: optionally selects in response to each compound) were also prepared. A 100 μl portion of the PPP of a rat to which the compound of the present invention was administered and the PPP containing the diluted compound of the present invention was mixed with the same volume of distilled water, and 5% trichloroacetic acid was further added thereto and mixed. After allowing to stand on ice for 10 minutes, a supernatant was recovered by a centrifugation operation. The supernatant was neutralized by adding 3 μl of 2 M Tris base thereto and mixing. A 150 μl portion of the P2Y12 protein expression C6-15 cell membrane fraction (200 μg/ml) was mixed with 50 μl of this trichloroacetic acid-treated PPP (depending on the compound, PPP diluted with 50 mM Tris-HCl (pH 7.4) containing 100 mM NaCl and 50 mM MgCl2 was used). Further, 50 μl of 0.75 nM [3H]-2-MeS-ADP (80 Ci/mmol, mfd. by Amersham Pharmacia Biotech) or 0.75 nM [33P]-2-MeS-ADP (2100 Ci/mmol, mfd. by Perkin Elmer) was added thereto and incubated at room temperature for 1 hour in 50 mM Tris-HCl (pH 7.4) containing 100 mM NaCl and 50 mM MgCl2, followed by recovery on a glass filter using a cell harvester. A microscintillator was added to the glass filter, and the radioactivity was measured using a liquid scintillation counter. Using the binding inhibition curve calculated from the measured results derived from PPP containing the serially diluted compound of the present invention as a standard curve, concentration of the compound of the present invention in PPP was converted from the measured results derived from the rat to which the compound of the present invention was administered.


The results are shown in Table 3. As a result of the evaluation by the above-mentioned method, it was revealed that the compound of the present invention shows good platelet aggregation inhibition activity by oral administration and also shows good pharmacokinetics.













TABLE 3








Dose




Compound to be tested
mg/kg
Inhibition %




















REx 1
30
11



REx 2
30
−7



Ex 82
10
75



Ex 87
10
72



Ex 114
3
66



Ex 125
30
89



Ex 146
30
72



Ex 271
30
89



Ex 297
30
48



Ex 380
30
74



Ex 407
30
54










EXAMPLES

The present invention is illustratively described based on examples, but the present invention is not restricted by these examples. In this connection, since novel substances are included in the starting compounds to be used in the Examples, production methods from such starting compounds are described as production examples.


In this connection, symbols in the production examples and Examples represent the following meanings (the same shall apply hereinafter).


Rf: production example number, Ex: Example number, No: compound number, Data: physical data (Sal: salt (No description means free form, and the numeral before the acid component shows compositional ratio. For example, when 2HCl is described, it shows that the compound is dihydrochloride. Oxa: oxalate, TFA: trifluoroacetate)), NMR: δ (ppm) of characteristic peak in 1H-NMR, EI: EI-MS (M+ unless otherwise noted), FAB: FAB-MS (Pos) (M++1 unless otherwise noted), ESI: ESI-MS (Pos) (M++1 unless otherwise noted), ACPI: ACPI-MS (Pos) (M++1 unless otherwise noted), ESI(Neg): ESI-MS (Neg) (M−1 unless otherwise noted), FAB(Neg): FAB-MS (Neg) (M−−1 unless otherwise noted), Me: methyl, Et: ethyl, nPr, normal propyl, iPr: isopropyl, cPr: cyclopropyl, nBu: normal butyl, iBu: isobutyl, tBu: tert-butyl, cBu: cyclobutyl, cPen: cyclopentyl; cHex: cyclohexyl, Ph: phenyl, Bn: benzyl, Boc: tert-butoxycarbonyl, Ac: acetyl, Bz: benzoyl, TBDMS: tert-butyldimethylsilyl. Syn: production method (The numeral shows that, similar to the Example compound having the number as its Example number, it was produced using the corresponding starting material. When Rf is added before the numeral, it shows that, similar to the production example compound having the number as its production example number, it was produced using the corresponding starting material. When two or more numerals are written, it shows that it was produced by carrying out corresponding production methods starting from the first numeral.), RSyn: production method (The numeral shows that, similar to the production example compound having the number as its production example number, it was produced using the corresponding starting material. When E is added before the numeral, it shows that, similar to the Example compound having the number as its Example number, it was produced using the corresponding starting material.).


Production Example 1

2.6 g of 1,1′-carbonyldiimidazole was added to a 30 ml DMF suspension of 4.0 g 7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid, followed by stirring at 100° C. for 13.5 hours. 10 ml of 28% aqueous ammonia was added thereto under ice-cooling, followed by stirring under ice-cooling for 75 minutes and at room temperature for 5 hours. After evaporation of the solvent under a reduced pressure, ethanol was added, and heating under reflux was carried out. After cooling to room temperature, the insoluble materials were collected by filtration and dried to obtain 3.7 g of 7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxamide.


Production Example 2

0.87 ml of triethylamine and 0.4 ml of isobutyl chloroformate were added to a 20 ml of dichloromethane solution of 1.0 g of 7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid at 0° C., followed by stirring at 0° C. for 30 minutes. Then, 315 mg of N,O-dimethylhydroxylamine hydrochloride was added thereto, followed by stirring at room temperature for 1 hour. Chloroform and aqueous saturated ammonium chloride were added to the reaction mixture, the layers were separated, and the organic layer was washed with aqueous saturated so iumchloride. After drying over anhydrous sodium sulfate and subsequent filtration, the solvent was evaporated under a reduced pressure. By purifying the resulting residue by silica gel column chromatography, 950 mg of 7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-N-methoxy-N-methyl-4-oxo-1,4-dihydroquinoline-3-carboxamide was obtained.


Production Example 3

5 g of 2-nitro-1-(2,4,5-trifluorophenyl)ethanone was dissolved in 100 ml of acetic anhydride, and 4.0 ml of triethyl orthoformate was added thereto at room temperature, followed by stirring at 130° C. for 3 hours and concentration under a reduced pressure. The resulting residue was dissolved in 100 ml of dichloromethane, and a 50 ml dichloromethane solution of 2.5 ml of cyclopentylamine was added under ice-cooling, followed by stirring at room temperature for 3 hours. Then, water was added, followed by extraction with chloroform. The organic layer was dried over anhydrous sodium sulfate and then concentrated under a reduced pressure. The resulting residue was dissolved in 80 ml of 1,4-dioxane, and a 20 ml dioxane solution of 3.6 ml 1,8-diazabicyclo[5.4.0]-7-undecene was added at room temperature, followed by stirring at room temperature for 3 hours. By pouring the resulting reaction mixture into ice-cooled water and collecting the insoluble materials by filtration, 1.8 g of 1-cyclopentyl-6,7-difluoro-3-nitroquinoline-4(1H)-one was obtained.


Production Example 4

Under ice-cooling, 11.5 g of sodium triacetoxyborohydride was added in small portions to a solution of 4.0 g of 3,4,5-trifluoroaniline and 3.6 ml cyclopentanone in 150 ml dichloroethane and 3.1 ml acetic acid, and, after rising to room temperature, stirred for 3.5 hours. Aqueous saturated sodium hydrogen carbonate was added thereto, followed by extraction with chloroform and subsequent drying over anhydrous sodium sulfate. After filtration, the solvent was evaporated under a reduced pressure, and the resulting residue was purified by silica gel column chromatography to obtain 5.4 g of N-cyclopentyl-3,4,5-trifluoroaniline.


Production Example 5

3.2 ml of diethyl(ethoxymethylene)malonate was added to 3.3 g of N-cyclopentyl-3,4,5-trifluoroaniline, followed by stirring at 130° C. for 4 hours. By purifying by silica gel column chromatography, 2.2 g of diethyl {[cyclopentyl(3,4,5-trifluorophenyl)amino]methylene}malonate was obtained.


Production Example 6

5.7 g of polyphosphoric acid was added to 2.2 g of diethyl {[cyclopentyl(3,4,5-trifluorophenyl)amino]methylene}malonate, followed by stirring at 140° C. for 40 minutes. The reaction mixture was poured into ice water, and the insoluble materials were collected by filtration. This was dissolved in chloroform, washed with water and aqueous saturated sodium chloride and dried over anhydrous sodium sulfate. After filtration, the solvent was evaporated to obtain 1.4 g of ethyl 1-cyclopentyl-5,6,7-trifluoro-4-oxo-1,4-dihydro quinoline-3-carboxylate.


Production Example 7

42% hydrofluoboric acid was added to 1.1 g of ethyl 1-cyclopentyl-5,6,7-trifluoro-4-oxo-1,4-dihydroquinoline-3-carboxylate, followed by heating at 90° C. for 20 hours. Water was added to the reaction mixture, and the thus formed insoluble materials were collected by filtration and dried to obtain 1.4 g of a boron compound. To 1.4 g of this boron compound were added 15 ml of DMSO and 0.97 ml of cyclohexylamine, followed by stirring at room temperature for 30 minutes. Water was added to the reaction mixture, and the insoluble materials were collected by filtration. After drying, 30 ml of ethanol and 15 ml of aqueous 1 M sodium hydroxide solution were added thereto, followed by stirring at 80° C. for 1.5 hours. After completion of the reaction, the insoluble materials were removed by filtration, water and diethyl ether were added to the filtrate to carry out separation of layers, and 1 M hydrochloric acid was added to the aqueous layer. The precipitate formed was collected by filtration and dried to obtain 1.0 g of 7-(cyclohexylamino)-1-cyclopentyl-5,6-difluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid.


Production Example 8

Under ice-cooling, 3.2 ml of n-butyl lithium (1.60 M hexane solution) was added to a 2.4 ml THF solution of 0.58 ml benzyl alcohol, followed by stirring for 1 hour. The solvent was evaporated under a reduced pressure, followed by the addition of 8.0 ml of toluene for suspension. The suspension prepared was added to a toluene suspension of 400 mg of 7-(cyclohexylamino)-1-cyclopentyl-5,6-difluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid, which was prepared in a separate container, followed by stirring at room temperature for 6 hours. Then, 1 M hydrochloric acid was added to the reaction mixture, followed by extraction with chloroform and washing with aqueous saturated sodium chloride. After drying over anhydrous sodium sulfate and subsequent filtration, the solvent was evaporated under a reduced pressure. By recrystallizing the resulting residue using ethyl acetate, 400 mg of 5-(benzyloxy)-7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid was obtained.


Production Example 9

900 mg of ethyl 1-cyclopentyl-7-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylate was dissolved in 6.4 ml of acetic acid, and 0.8 ml of 6 M hydrochloric acid was added, followed by overnight stirring at 120° C. The resulting reaction mixture was cooled to room temperature, and the insoluble materials were collected by filtration and washed with water to obtain 710 mg of 1-cyclopentyl-7-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid.


Production Example 10

1.02 g of 1-cyclobutylethylamine hydrochloride and 1.05 ml of triethylamine were added under ice-cooling to a 15 ml THF solution of 2.0 g of ethyl 2-(2-chloro-4,5-difluorobenzoyl)-3-ethoxyacrylate, followed by overnight stirring at room temperature. Water was added to the resulting reaction mixture, followed by extraction with ether and washing with water and aqueous saturated sodium chloride. After drying over anhydrous magnesium sulfate, concentration under a reduced pressure was carried out. 315 mg of 55% sodium hydride was added under ice-cooling to a 30 ml dioxane solution of the resulting residue, followed by overnight stirring at 80° C. The reaction mixture was poured into 1 M hydrochloric acid, followed by extraction with chloroform and washing with water and aqueous saturated sodium chloride. After drying over anhydrous sodium sulfate and subsequent concentration under a reduced pressure, the resulting residue was purified by silica gel column chromatography to obtain 1.13 g of ethyl 1-(1-cyclobutylethyl)-6,7-difluoro-4-oxo-1,4-dihydroquinoline-3-carboxylate.


In the same manner as in the Production Examples 1 to 10, Production Example compounds 11 to 27 shown in Tables 4 to 9 were produced using corresponding starting materials, respectively. Structures and physicochemical date of Production Example compounds are shown in Tables 4 to 9.


Example 1

250 mg of 3-amino-7-(cyclohexylamino)-1-cyclopentyl-6-fluoroquinoline-4(1H)-one and 127 mg of 4-ethoxy-4-oxobutanoic acid were dissolved in 20 ml of DMF, and 170 mg of N-[3-(dimethylamino)propyl]-N′-ethylcarbodiimide hydrochloride and 160 mg of 1-hydroxybenzotriazole were added, followed by overnight stirring at room temperature. By adding water to the reaction mixture and collecting the insoluble materials by filtration, 220 mg of ethyl 4-{[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]amino}-4-oxobutanoate was obtained.


Example 2

200 mg of ethyl 4-{[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]amino}-4-oxobutanoate was dissolved in 2.0 ml of THF and 2.0 ml of ethanol, and 1.3 ml of aqueous 1M sodium hydroxide solution was added, followed by stirring at room temperature for 4 hours. After adding 1 M hydrochloric acid and water thereto, the insoluble materials were collected by filtration to obtain 180 mg of 4-{[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]amino}-4-oxobutanoic acid.


Example 3

200 mg of diethyl {(E)-2-[7-(cyclohexylamino)-1-(1-ethylpropyl)-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]vinyl}phosphonate was dissolved in 2.0 ml of chloroform, and 0.4 ml of bromotrimethylsilane was added, followed by overnight stirring at room temperature. Ethanol was added to the reaction mixture, followed by concentration under a reduced pressure. Ethyl acetate was added to the resulting residue, and the insoluble materials were collected by filtration to obtain 120 mg of {(E)-2-[7-(cyclohexylamino)-1-(1-ethylpropyl)-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]vinyl}phosphonic acid hydrobromide.


Example 4

169 mg of sodium triacetoxyborohydride was added to a mixed solution 10 ml of 1,2-dichloroethane and 0.05 ml of acetic acid of 142 mg 7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carbaldehyde and 66 mg of 4-aminophenol, followed by stirring for 24 hours. Aqueous saturated sodium hydrogen carbonate was added thereto, followed by extraction with chloroform. After drying over anhydrous sodium sulfate and subsequent filtration, concentration under a reduced pressure was carried out. The resulting residue was purified by silica gel column chromatography and then crystallized from ethyl acetate to obtain 46 mg of [7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-3-{[(4-hydroxyphenyl)amino]methyl}quinolin-4(1H)-one.


Example 5

250 mg of 3-(aminomethyl)-7-(cyclohexylamino)-1-(1-ethylpropyl)-6-fluoroquinolin-4(1H)-one hydrochloride was dissolved in 25 ml of THF, and 0.11 ml of diethyl (2-oxopropyl)phosphonate and 123 mg of sodium triacetoxyborohydride, 0.16 ml of triethylamine and 1.25 ml of acetic acid were added in that order, followed by overnight stirring at room temperature. Water was added, and the insoluble materials were collected by filtration and then purified by silica gel column chromatography to obtain 135 mg of diethyl[2-({[7-(cyclohexylamino)-1-(1-ethylpropyl)-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]methyl}amino)propyl]phosphonate.


Example 6

170 mg of ethyl 4-({[7-(cyclohexylamino)-1-(1-ethylpropyl)-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]methyl}amino)butanoate was dissolved in 2.0 ml of pyridine, and 0.040 ml of acetic anhydride was added, followed by overnight stirring at room temperature. After concentrating the reaction mixture under a reduced pressure, water was added to the resulting residue, followed by extraction with chloroform. The organic layer was dried over anhydrous sodium sulfate and then filtered and concentrated under a reduced pressure. By purifying the resulting residue by silica gel column chromatography, 165 mg of ethyl 4-(acetyl {[7-(cyclohexylamino)-1-(1-ethylpropyl)-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]methyl}amino)butanoate was obtained.


Example 7

180 mg of 4-nitrophenyl chloroformate was dissolved in 3.0 ml of dichloromethane, and 140 mg of ethyl 3-aminopropanoate hydrochloride and 0.15 ml of pyridine were added, followed by overnight stirring at room temperature. Water was added to the reaction mixture, followed by extraction with chloroform. The organic layer was washed with aqueous saturated sodium chloride, dried over anhydrous sodium sulfate, filtered and then concentrated under a reduced pressure. By purifying the resulting residue by silica gel column chromatography, 180 mg of ethyl 3-{[(4-nitrophenoxy)carbonyl]amino}propanoate was obtained. 180 mg of ethyl 3-{[(4-nitrophenoxy)carbonyl]amino}propanoate was dissolved in 2.0 ml of dichloromethane, and 220 mg of 3-amino-7-(cyclohexylamino)-1-(1-ethylpropyl)-6-fluoroquinolin-4(1H)-one and 0.15 ml of pyridine were added, followed by overnight stirring at room temperature. Water was added, followed by extraction with chloroform. The organic layer was washed with aqueous saturated sodium chloride, dried over anhydrous sodium sulfate and then filtered and concentrated under a reduced pressure. By purifying the resulting residue by silica gel column chromatography, 120 mg of ethyl 3-[({[7-(cyclohexylamino)-1-(1-ethylpropyl)-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]amino}carbonyl)amino]propanoate was obtained.


Example 8

287 mg of ethyl[(5-chloro-2-thienyl)sulfonyl]carbamate was dissolved in 5.0 ml of toluene, and 250 mg of 3-amino-7-(cyclohexylamino)-6-fluoro-1-isopropylquinolin-4(1H)-one was added, followed by overnight stirring at 110° C. The reaction mixture was cooled to room temperature and concentrated under a reduced pressure. Then, ethyl acetate was added and the insoluble materials were collected by filtration, thereby obtaining 280 mg of 5-chloro-N-({[7-(cyclohexylamino)-6-fluoro-1-isopropyl-4-oxo-1,4-dihydroquinolin-3-yl]amino}carbonyl)thiophene-2-sulfonamide.


Example 9

224 mg of 2-amino-N-[7-(cyclohexylamino)-1-(1-ethylpropyl)-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]acetamide hydrochloride was dissolved in 5.0 ml of DMF, and 228 mg of potassium carbonate and 0.18 ml of ethyl bromoacetate were added, followed by overnight stirring at 60° C. The reaction mixture was cooled to room temperature, water was added, and the insoluble materials were collected by filtration to obtain 35 mg of diethyl 2,2′-[(2-{[7-(cyclohexylamino)-1-(1-ethylpropyl)-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]amino}-2-oxoethyl)imino]diacetate.


Example 10

150 mg of ethyl {[7-(cyclohexylamino)-1-(1-ethylpropyl)-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]amino}acetate was dissolved in 3.0 ml of THF, and 0.060 ml of triethylamine and 0.060 ml of ethyl 5-chloro-5-oxopentanoate were added, followed by overnight stirring at room temperature. Water was added to the reaction mixture, followed by extraction with chloroform. The resulting organic layer was washed with aqueous saturated sodium chloride, dried over anhydrous sodium sulfate and then concentrated under a reduced pressure. By purifying the resulting residue by silica gel column chromatography, 199 mg of ethyl 5-[[7-(cyclohexylamino)-1-(1-ethylpropyl)-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl](2-ethoxy-2-oxoethyl)amino]-5-oxopentanoate was obtained.


Example 11

200 mg of ethyl (2E)-3-[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]acrylate was dissolved in 4.0 ml of ethanol, and 50 mg of palladium-carbon was added, followed by overnight stirring at room temperature in an atmosphere of hydrogen. The reaction mixture was filtered using celite and concentrated under a reduced pressure to obtain 200 mg of ethyl (3-[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]propanoate.


Example 12

213 μl of diisopropyl azodicarboxylate was added to a 5.0 ml dichloromethane solution of 263 mg of benzyl (2R)-2-hydroxy-3-phenylpropanoate and 270 mg of triphenylphosphine at 0° C., followed by stirring for 15 minutes. Then, 177 mg of 7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-3-(hydroxymethyl)quinolin-4(1H)-one was added thereto, followed by stirring at room temperature for 4 hours. Water was added to the reaction mixture, followed by extraction with EtOAc and washing with aqueous saturated sodium chloride. After drying over anhydrous sodium sulfate and subsequent evaporation under a reduced pressure, the residue was purified by silica gel column chromatography to obtain 160 mg of benzyl (2S)-2-{[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]oxy}-3-phenylpropanoate.


Example 13

690 mg of potassium carbonate and 363 mg of 4-fluorobenzonitrile were added to a 10 ml DMF solution of 344 mg of 7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-3-hydroxyquinolin-4(1H)-one, followed by overnight stirring at 80° C. After completion of the reaction and subsequent cooling to room temperature, aqueous saturated ammonium chloride was added to the reaction mixture, followed by extraction with ethyl acetate. After drying over anhydrous sodium sulfate and subsequent evaporation under a reduced pressure, the residue was purified by silica gel column chromatography to obtain 100 mg of 4-{[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]oxy}benzonitrile.


Example 14

5.0 ml of ethanol and 1.5 ml of aqueous 6 M sodium hydroxide solution were added to 93 mg of 4-{[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]oxy}benzonitrile, followed by heating under reflux for 2 days. After cooling, the reaction system was neutralized with 1 M hydrochloric acid. Water was added and the solid precipitated was collected by filtration. By crystallizing the resulting solid from ethyl acetate-hexane, 65 mg of 4-{[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]oxy}benzoic acid was obtained.


Example 15

840 mg of 7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carbaldehyde was dissolved in 40 ml of chloroform, and 0.47 ml of trimethylsilyl cyanide and 0.05 ml of triethylamine was added under ice-cooling, followed by stirring at room temperature for 5.5 hours. After stirring at room temperature for 1.5 hours after further adding 0.06 ml of trimethylsilyl cyanide, 0.06 ml of trimethylsilyl cyanide was further added thereto, followed by stirring at room temperature for 2 days. The resulting precipitate was filtered and washed with chloroform to obtain a solid. The resulting solid was dissolved in 13 ml of concentrated hydrochloric acid, followed by stirring at 100° C. for 2.5 hours. After cooling to room temperature, water was added, followed by extraction with chloroform, drying over anhydrous sodium sulfate and then concentration under a reduced pressure. The resulting residue was purified by silica gel column chromatography to obtain crude product of [7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl](hydroxy)acetic acid. The resulting crude product was washed with water:methanol (1:2) and ethyl acetate. Ethyl acetate and aqueous saturated sodium hydrogen carbonate were added to the resulting solid to carry out layer separation operation. 1 M hydrochloric acid was added to the aqueous layer, followed by extraction with ethyl acetate and concentration under a reduced pressure. A mixed solvent of THF and water was added to the resulting residue and the insoluble materials were collected by filtration to obtain 149 mg of [7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl](hydroxy)acetic acid.


Example 16

52 mg of [7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl](hydroxy)acetic acid was dissolved in 10 ml of methanol, and 0.4 ml of concentrated sulfuric acid was added, followed by stirring at room temperature for 1 hour. Aqueous saturated sodium hydrogen carbonate was added to the reaction mixture, followed by extraction with ethyl acetate, washing with aqueous saturated sodium chloride and concentration under a reduced pressure. The resulting residue was recrystallized from aqueous methanol to obtain 53 mg of methyl[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl](hydroxy)acetate.


Example 17

146 mg of methyl[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl](hydroxy)acetate was dissolved in 10 ml of THF, and 46 mg of 60% sodium hydride was added under ice-cooling, followed by stirring at room temperature for 30 minutes. Then, 58 μl of ethyl bromoacetate was added to the reaction mixture, followed by stirring at room temperature for 5 hours. 46 mg of 60% sodium hydride and 10 ml of THF were further added under ice-cooling, followed by stirring at room temperature for 2 hours. Then, 58 μl of ethyl bromoacetate was added thereto, followed by stirring at room temperature for 17 hours. Aqueous saturated sodium hydrogen carbonate was added to the reaction mixture, followed by extraction with ethyl acetate. Then, the organic layer was washed with aqueous saturated sodium chloride. After drying over anhydrous sodium sulfate, concentration was carried out under a reduced pressure. The resulting residue was purified by silica gel column chromatography to obtain 66 mg of methyl[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl](2-ethoxy-2-oxoethoxy)acetate.


Example 18

13 g of diethyl {(E)-2-[7-(cyclohexylamino)-1-(1-ethylpropyl)-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]vinyl}phosphonate was dissolved in 150 ml of chloroform, and 27.2 ml of bromotrimethylsilane was added, followed by overnight stirring at room temperature. Ethanol was added to the reaction mixture, followed by concentration under a reduced pressure. Aqueous 1 M sodium hydroxide solution and ether were added to the resulting residue to carry out layer separation operation. Concentrated hydrochloric acid was added to the aqueous layer, followed by stirring at room temperature for 2 hours. Then, the insoluble materials were collected by filtration and washed with water to obtain 10.32 g of {(E)-2-[7-(cyclohexylamino)-1-(1-ethylpropyl)-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]vinyl}phosphonic acid.


Example 19

428 mg of (methoxymethyl)triphenylphosphonium chloride was dissolved in 5 ml of THF, and 1.2 ml of 1.6 M n-butyl lithium hexane solution was added under ice-cooling in an atmosphere of argon, followed by stirring at the same temperature for 30 minute. A 5 ml THF solution of 178 mg of 7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carbaldehyde was added under ice-cooling thereto, followed by stirring at the same temperature for 15 minutes and then stirring at room temperature for 3 hours. The reaction mixture was poured into ice water, followed by extraction with ethyl acetate, drying over anhydrous sodium sulfate and then concentration under a reduced pressure. The resulting residue was dissolved in 10 ml of dioxane, and 5 ml of a 4 M hydrogen chloride dioxane solution was added, followed by stirring at room temperature for 2 hours. The reaction mixture was poured into an ice-cooled aqueous saturated sodium hydrogen carbonate, followed by extraction with ethyl acetate, drying over anhydrous sodium sulfate and then concentration under a reduced pressure. By purifying the resulting residue by silica gel column chromatography, 239 mg of crude product of [7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl)acetaldehyde was obtained. The resulting crude product was dissolved in 10 ml of ethanol, and 75 mg of sodium borohydride was added, followed by stirring at room temperature for 1 hour. Water was added to the reaction mixture, followed by extraction with ethyl acetate, drying over anhydrous sodium sulfate and then concentration under a reduced pressure. The resulting residue was purified by silica gel column chromatography and crystallized from ethyl acetate to obtain 18 mg of 7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-3-(2-hydroxyethyl)quinolin-4(1H)-one.


Example 20

856 mg of (methoxymethyl)triphenylphosphonium chloride was dissolved in 10 ml of THF, and 1.8 ml of a 1.6 M n-butyl lithium hexane solution was added under ice-cooling in an atmosphere of argon, followed by stirring at the same temperature for 30 minute. A 10 ml THF solution of 356 mg of 7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carbaldehyde was added under ice-cooling thereto, followed by stirring at room temperature for 3 hours. The reaction mixture was poured into ice water, followed by extraction with ethyl acetate, drying over anhydrous sodium sulfate and then concentration under a reduced pressure. The resulting residue was purified by column chromatography to obtain 552 mg crude product of 7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-3-[2-methoxyvinyl]quinolin-4(1H)-one. 159 mg of the resulting crude product was dissolved in 14 ml of dioxane, and 7 ml of a 4 M hydrogen chloride dioxane solution was added, followed by stirring at room temperature for 0.5 hour. The reaction mixture was concentrated under a reduced pressure, and the resulting residue was dissolved in 6 ml of 2-methyl-2-propanol, 1 ml of acetonitrile and 2 ml of water. Then, 0.26 ml of 2-methyl-2-butene, 78 mg of sodium dihydrogenphosphate dihydrate and 228 mg of a 79% sodium chlorite aqueous solution were added under ice-cooling, followed by stirring at room temperature for 14 hours. Water was added to the reaction mixture, followed by extraction with chloroform, drying over anhydrous sodium sulfate and then concentration under a reduced pressure. The resulting residue was purified by silica gel column chromatography and crystallized from ethyl acetate to obtain 5 mg of 7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]acetic acid.


Example 21

199 mg of 7-(cyclohexylamino)-1-(1-ethylpropyl)-6-fluoro-3-(4-hydroxybutyl)quinolin-4(1H)-one was dissolved in 11 ml of 1,2-dichloroethane, and 257 mg of triphenylphosphine and 405 mg of carbon tetrabromide were added at room temperature, followed by stirring for 15 minutes. Aqueous saturated sodium hydrogen carbonate was added to the reaction mixture, followed by extraction with chloroform, washing with aqueous saturated sodium chloride, drying over anhydrous sodium sulfate and then concentration under a reduced pressure. The resulting residue was purified by a chromatography to obtain 78 mg of 3-(4-bromobutyl)-7-(cyclohexylamino)-1-(1-ethylpropyl)-6-fluoro quinolin-4(1H)-one.


Example 22

To 557 mg of 3-(4-bromobutyl)-7-(cyclohexylamino)-1-(1-ethylpropyl)-6-fluoroquinolin-4(1H)-one was added 5 ml of triethylphosphite, followed by stirring at 160° C. for 4 hours. The reaction mixture was concentrated under a reduced pressure, and the resulting residue was purified by a column chromatography to obtain 240 mg of diethyl {4-[7-(cyclohexylamino)-1-(1-ethylpropyl)-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]butyl}phosphonate.


Example 23

To 2 ml of a 2 M isopropyl magnesium chloride THF solution was added 2 ml of THF and, at −78° C., 0.71 ml of diethyl[bromo(difluoro)methyl]phosphonate, followed by stirring at the same temperature for 5 minutes. A 10 ml THF solution of 358 mg of 7-(cyclohexylamino)-1-(1-ethylpropyl)-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carbaldehyde was added dropwise to the reaction mixture and, after gradual temperature rising to room temperature, this was stirred for 2.5 hours. Aqueous saturated sodium chloride was added to the reaction mixture, followed by extraction with chloroform and ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate and then concentrated under a reduced pressure. Methanol was added to the residue, insoluble materials were filtered, and the resulting filtrate was evaporated under a reduced pressure. By purifying the resulting residue by a column chromatography, 257 mg of diethyl {2-[7-(cyclohexylamino)-1-(1-ethylpropyl)-6-fluoro-4-oxo-1,4-dihydro quinolin-3-yl]-1,1-difluoro-2-hydroxyethyl}phosphonate.


Example 24

1.0 g of 7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carbaldehyde was dissolved in 20 ml of DMF, and 2.0 g of potassium carbonate and 2.8 ml of ethyl(diethoxyphosphoryl)acetate were added, followed by overnight stirring at 60° C. The resulting reaction mixture was cooled to room temperature, water was added, and then the insoluble materials were collected by filtration to obtain 1.2 g of ethyl (2E)-3-[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]acrylate.


Example 25 and Example 26

500 mg of {(E)-2-[7-(cyclohexylamino)-1-(1-ethylpropyl)-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]vinyl}phosphonic acid was dissolved in 10 ml of acetonitrile, and 86 mg of sodium iodide, 0.51 ml of 1,8-diazabicyclo[5.4.0]-7-undecene, 194 mg of tetrabutylammonium hydrogensulfate and 0.53 ml of chloromethyl pivalate were added in that order, followed by overnight stirring at 80° C. Aqueous saturated ammonium chloride was added to the reaction mixture, followed by extraction with chloroform. The organic layer was washed with aqueous saturated sodium chloride, dried over anhydrous sodium sulfate and then evaporated under a reduced pressure. By purifying the resulting residue by silica gel column chromatography, 400 mg of bis{[(2,2-dimethylpropanoyl)oxy]methyl}{(E)-2-[7-(cyclohexylamino)-1-(1-ethylpropyl)-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]vinyl}phosphonate (Example 25) and 190 mg of {[{(E)-2-[7-(cyclohexylamino)-1-(1-ethylpropyl)-6-fluoro-4-oxo-1,4-dihydro-3-quinolinyl]vinyl}(hydroxy)phosphoryl]oxy}methyl pivalate (Example 26) were obtained.


Example 27

To a 5.0 ml DMF solution of 144 mg of 7-(cyclohexylamino)-6-fluoro-3-hydroxy-1-isopropylquinolin-4(1H)-one were added 313 mg of potassium carbonate and 100 μl of ethyl bromoacetate in that order, followed by overnight stirring at room temperature. Aqueous saturated ammonium chloride was added to the reaction mixture, followed by extraction with ethyl acetate. After drying over anhydrous sodium sulfate and subsequent evaporation under a reduced pressure, the residue was purified by silica gel column chromatography to obtain 159 mg of ethyl {[7-(cyclohexylamino)-6-fluoro-1-isopropyl-4-oxo-1,4-dihydroquinolin-3-yl]oxy}acetate.


Example 28

To a 2.9 ml dioxane solution of tert-butyl (2-{[7-(cyclohexylamino)-1-(1-ethylpropyl)-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]amino}-2-oxoethyl)carbamate was added 3.0 ml of a 4M hydrogen chloride dioxane solution, followed by overnight stirring at room temperature. The insoluble materials were collected by filtration to obtain 550 mg of 2-amino-N-[7-(cyclohexylamino)-1-(1-ethylpropyl)-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]acetamide hydrochloride.


Example 29

To a 90 ml DMF solution of 15.0 g of 7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid was added 9.9 g of 1,1′-carbonyldiimidazole, followed by stirring at 80° C. for 24 hours. After cooling, the reaction mixture was poured into ice water, and the solid precipitated was collected by filtration. Next, 1.9 g of sodium borohydride was added at 0° C. to a mixed solution of 200 ml THF and 100 ml water of the resulting solid, followed by stirring at the same temperature for 2 hours. Water was added, the solvent was evaporated under a reduced pressure, and the insoluble materials were collected by filtration to obtain 13.8 g of 7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-3-(hydroxymethyl)quinolin-4(1H)-one.


Example 30

After adding 0.32 ml of DMSO to a 7.0 ml dichloromethane solution of 0.20 ml of oxalyl dichloride at −78° C. and stirring for 30 minutes, a dichloromethane solution of 330 mg of N-[7-(cyclohexylamino)-1-(1-ethylpropyl)-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]-2-(hydroxymethyl)butanamide was added at −78° C., followed by stirring for 30 minutes. Next, 1.2 ml of triethylamine was added thereto, and the temperature was risen from −78° C. to room temperature spending 2 hours. Aqueous saturated sodium chloride was added to the reaction mixture, followed by extraction with ethyl acetate, drying over anhydrous sodium sulfate, and evaporation under a reduced pressure, thereby obtaining 320 mg of crude product of N-[7-(cyclohexylamino)-1-(1-ethylpropyl)-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]-2-formylbutanamide. To a 6.4 ml dichloromethane solution of 320 mg of the resulting crude product was added 290 mg of methyl(triphenylphosphoranilidene)acetate, followed by overnight stirring at room temperature. By evaporating the reaction mixture under a reduced pressure and purifying the resulting mixture by silica gel column chromatography, 220 mg of methyl (2E)-4-({[7-(cyclohexylamino)-1-(1-ethylpropyl)-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]amino}carbonyl)hex-2-enoate was obtained.


Example 31

To a 8 ml THF solution of 400 mg of ethyl 3-[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]propanoate was added 40 mg of lithium aluminum hydride at 0° C., followed by stirring for 2 hours. Water was added to the reaction mixture, followed by and filteraion through celite. After evaporation under a reduced pressure, the resulting residue was purified by silica gel column chromatography to obtain 288 mg of 7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-3-(3-hydroxypropyl)quinolin-4(1H)-one.


Example 32

To a 5 ml 1,4-dioxane solution of 300 mg of {[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]oxy}acetonitrile was added 0.8 ml of tributyltin azide, followed by heating under reflux for 2 days. After cooling to room temperature, aqueous 1M sodium hydroxide solution and ether were added, followed by layer separation operation. To the aqueous layer was added 1 M hydrochloric acid, followed by extraction with chloroform and washing with aqueous saturated sodium chloride. After drying over anhydrous sodium sulfate, the solvent was evaporated under a reduced pressure. By adding ether to the resulting residue and collecting the insoluble materials by filtration, 70 mg of 7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-3-(1H-tetrazol-5-ylmethoxy)quinolin-4(1H)-one was obtained.


Example 33

To a 30 ml dichloromethane suspension of 3.69 g of 7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxamide were added at −78° C. 7.0 ml of triethylamine and a 10 ml dichloromethane solution of 4.0 ml of trifluoroacetic anhydride. After gradually rising the temperature, it was stirred at room temperature for 2 days. After adding water, it was extracted with chloroform, followed by drying over anhydrous sodium sulfate. After filtration, the solvent was evaporated under a reduced pressure and the resulting residue was purified by silica gel column chromatography. After adding a mixed solvent of 30 ml of THF, 30 ml of methanol and 10 ml of water to the resulting solid, 2.3 g of potassium carbonate was added thereto under ice-cooling. After stirring at room temperature for 15 hours, 1.0 g of potassium carbonate was added thereto, followed by stirring at room temperature for 4 days. After evaporating the solvent under a reduced pressure, water was added, followed by extraction with chloroform. After drying over anhydrous sodium sulfate and subsequent filtration, the solvent was evaporated under a reduced pressure. By washing the resulting residue with ethyl acetate, 2.62 g of 7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carbonitrile was obtained.


Example 34

10 ml of Raney nickel was washed three times with ethanol. 30 ml of ethanol, 3 ml of aqueous ammonia and 2.5 g of 7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carbonitrile were added thereto, followed by overnight stirring in an atmosphere of hydrogen. After addition of chloroform and subsequent filtration using celite, the solvent was evaporated under a reduced pressure. The resulting residue was dissolved in 20 ml of THF, a 10 ml THF solution of 1.8 g of di-tert-butyl dicarbonate was added under ice-cooling, followed by overnight stirring at room temperature. A 10 ml THF solution of 1.0 g of di-tert-butyl dicarbonate was added thereto under ice-cooling, followed by stirring at room temperature for 3 days. A 10 ml THF solution of 1.0 g of di-tert-butyl dicarbonate was added thereto under ice-cooling, followed by overnight stirring at room temperature. After evaporation of the solvent under a reduced pressure and subsequent purification by silica gel column chromatography, the resulting solid was recrystallized from hexane-ethyl acetate to obtain 1.22 g of tert-butyl {[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]methyl}carbamate.


Example 35

To 5.50 g of 7-(cyclohexylamino)-1-(1-ethylpropyl)-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carbonitrile were added 50 ml of ethanol, 3.0 ml of concentrated hydrochloric acid and 0.60 g of platinum oxide, followed by overnight stirring in an atmosphere of hydrogen. After adding water, celite filtration was carried out and the solvent was evaporated under a reduced pressure. The resulting residue was dissolved by adding 30 ml of water and 20 ml of THF, and 4.0 g of sodium hydrogen carbonate and 4.5 g of di-tert-butyl dicarbonate were added under ice-cooling, followed by stirring under ice-cooling for 1 hour and overnight at room temperature. After evaporation of the solvent under a reduced pressure, water was added, followed by extraction with chloroform and drying over anhydrous sodium sulfate. After filtration, the solvent was evaporated under a reduced pressure and the resulting residue was purified by silica gel column chromatography to obtain 5.72 g of tert-butyl {[7-(cyclohexylamino)-1-(1-ethylpropyl)-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]methyl}carbamate.


Example 36

To 0.31 g of 7-(cyclohexylamino)-6-fluoro-4-oxo-1-pyrrolidin-3-yl-1,4-dihydroquinoline-3-carbonitrile hydrochloride were added 5 ml of ethanol, 0.2 ml of concentrated hydrochloric acid and 0.10 g of platinum oxide, followed by overnight stirring in an atmosphere of hydrogen. After adding water, celite filtration was carried out and the solvent was evaporated under a reduced pressure. By purifying the resulting residue by an ODS column chromatography, 256 mg of 3-(aminomethyl)-7-(cyclohexylamino)-6-fluoro-1-pyrrolidin-3-ylquinolin-4(1H)-one hydrochloride was obtained.


Example 37

To a 40 ml DMSO solution of 2.0 g of 1-cyclopentyl-6,7-difluoro-3-nitroquinolin-4(1H)-one was added 2.3 ml of cyclohexylamine, followed by overnight stirring at 90° C. The reaction mixture was cooled to room temperature and poured into ice-cooled water, and then the insoluble materials were collected by filtration. By recrystallizing the resulting solid from ethanol, 2.5 g of 7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-3-nitroquinolin-4(1H)-one was obtained.


Example 38

To a 4 ml ethanol solution of 220 mg of 3-amino-7-(cyclohexylamino)-1-(1-ethylpropyl)-6-fluoroquinolin-4(1H)-one was added 105 mg of 1H-1,2,3-benzotriazol-1-ylmethanol, followed by overnight stirring at room temperature. Next, 48 mg of sodium borohydride was added to the reaction mixture, followed by stirring for 3 hours. By adding water to the resulting reaction mixture and collecting the insoluble materials by filtration, 100 mg of 7-(cyclohexylamino)-1-(1-ethylpropyl)-6-fluoro-3-(methylamino)quinolin-4(1H)-one was obtained.


Example 39

To a 100 ml dichloromethane solution of 13.8 g of 7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-3-(hydroxymethyl)quinolin-4(1H)-one was added 67.0 g of manganese dioxide at room temperature, followed by overnight stirring. After completion of the reaction and subsequent filtration using celite, the filtrate was evaporated under a reduced pressure. By crystallizing the resulting solid from ethyl acetate, 13.0 g of 7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carbaldehyde was obtained.


Example 40

6.1 g of metachloroperbenzoic acid was gradually added to a 100 ml of dichloromethane solution of 8.0 g of 7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carbaldehyde at room temperature, followed by stirring for 2 hours. Aqueous saturated sodium hydrogen carbonate and aqueous sodium hydrogenthiosulfate were added to the reaction mixture, followed by stirring for 30 minutes and then extraction with chloroform. After drying over anhydrous sodium sulfate and subsequent evaporation under a reduced pressure, the residue was purified


(Production Methods)


The compound of the present invention and a pharmaceutically acceptable salt thereof may be produced by employing various conventionally known synthesis methods making use of the characteristics based on its basic skeleton or kind of the substituent groups. Typical production methods are exemplified in the following. In this connection, depending on the kinds of functional group, there is an effective case from the production technology point of view to replace said functional group with an appropriate protecting group, namely a group which may be easily converted into said functional group, at the stage of starting material to intermediate. Thereafter, the desired compound may be obtained by removing the protecting group as occasion demands. Examples of the functional group include hydroxyl group, carboxyl group, amino group and the like, and as their protecting groups, the protecting groups described for example in “Protective Groups in Organic Synthesis (third edition)” edited by Greene and Wuts, may be cited, which may be optionally used in response to the reaction conditions.


First Production Method




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(In the formulae, L1 represents a leaving group such as halogen, —O-methanesulfonyl, —O-p-toluenesulfonyl or the like. The same shall apply hereinafter.) by silica gel column chromatography to obtain 7.7 g of 7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-3-hydroxyquinoline-4(1H)-one.


Example 41

To a 2.0 ml acetic acid solution of 150 mg of 7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carbaldehyde were added 60 mg of 2-thioxo-1,3-thiazoline-4-one and 40 mg of sodium acetate in that order, followed by overnight stirring at 100° C. The reaction mixture was cooled to room temperature and evaporated under a reduced pressure. Ethyl acetate was added, and the insoluble materials were collected by filtration to obtain 173 mg of 7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-3-[(Z)-(4-oxo-2-thioxo-1,3-thiazolidin-5-ylidene)methyl]quinolin-4(1H)-one.


Example 42

To a 15 ml THF solution of 762 mg of 3-(3-{[tert-butyl(dimethyl)silyl]oxy}propoxy)-7-(cyclohexylamino)-1-cyclopentyl-6-fluoroquinoline-4(1H)-one was added 1.5 ml of a 1 M tetrabutylammonium fluoride THF solution at room temperature, followed by stirring for 2 hours. Water was added to the reaction mixture, followed by extraction with ethyl acetate and washing with aqueous saturated sodium chloride. After drying over anhydrous sodium sulfate, evaporation was carried out under a reduced pressure. By purifying the residue by silica gel column chromatography, 273 mg of 7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-3-(3-hydroxypropoxy)quinolin-4(1H)-one was obtained.


Example 43

To a 10 ml THF solution of 500 mg of 7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-N-methoxy-N-methyl-4-oxo-1,4-dihydroquinoline-3-carboxamide was added 1.2 ml of a 1 M methyl lithium THF solution, followed by stirring at room temperature for 3 days. Water was added to the reaction mixture to carry out celite filtration. After evaporation under a reduced pressure, the resulting residue was purified by silica gel column chromatography to obtain 150 mg of 3-acetyl-7-(cyclohexylamino)-1-cyclopentyl-6-fluoroquinolin-4(1H)-one.


Example 44

To a 5.0 ml dichloromethane solution of 500 mg of 7-(cyclohexylamino)-1-(1-ethylpropyl)-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carbaldehyde were added 0.23 ml of diethyl phosphite and 0.22 ml of 1,8-diazabicyclo[5.4.0]-7-undecene at −40° C., followed by overnight stirring at room temperature. Aqueous saturated ammonium chloride was added to the reaction mixture, followed by extraction with chloroform and then washing with aqueous saturated sodium chloride. After drying over anhydrous sodium sulfate and subsequent evaporation under a reduced pressure, the resulting residue was purified by silica gel column chromatography to obtain 400 mg of diethyl [[7-(cyclohexylamino)-1-(1-ethylpropyl)-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl](hydroxy)methyl]phosphonate.


Example 45

To a 3.2 ml DMF solution of 160 mg of ethyl {[7-(cyclohexylamino)-1-(1-ethylpropyl)-6-fluoro-4-oxo-1,4-dihydro quinolin-3-yl]amino}acetate were added 0.05 ml of benzyl bromide and 75 mg of potassium carbonate, followed by overnight stirring at room temperature. By adding water to the reaction mixture and collecting the insoluble materials by filtration, 200 mg of ethyl {benzyl[7-(cyclohexylamino)-1-(1-ethylpropyl)-6-fluoro-4-oxo-1,4-dihydro quinolin-3-yl]amino}acetate was obtained.


Example 46

To a 4.2 ml THF solution of 210 mg of (2E)-3-{7-[(cyclopropylmethyl)amino]-6-fluoro-1-isopropyl-4-oxo-1,4-dihydroquinolin-3-yl}acrylic acid was added 120 mg of 1,1′-carbonyldiimidazole, followed by overnight stirring at room temperature. Water was added to the reaction mixture and the insoluble materials were collected by filtration. The resulting solid was dissolved in 4.2 ml of DMF, and 0.11 ml of 1,8-diazabicyclo[5.4.0]-7-undecene and 150 mg of 5-chlorothiophene-2-sulfonamide were added, followed by overnight stirring at 80° C. By adding water to the resulting reaction mixture and collecting the insoluble materials by filtration, 145 mg of (2E)-N-[(5-chloro-2-thienyl)sulfonyl]-3-{7-[(cyclopropylmethyl)amino]-6-fluoro-1-isopropyl-4-oxo-1,4-dihydroquinolin-3-yl}acrylamide was obtained.


Example 47

Under ice-cooling, 2.0 ml of trifluoroacetic acid was added to a 5 ml dichloromethane solution of 0.20 g of tert-butyl {[7-(cyclohexylamino)-6-fluoro-4-oxo-1-(tetrahydrofuran-3-yl)-1,4-dihydroquinolin-3-yl]methyl}carbamate. After stirring under ice-cooling for 1.5 hours and at room temperature overnight, the solvent was evaporated under a reduced pressure. By purifying the resulting residue by an ODS column chromatography, 184 mg of 3-(aminomethyl)-7-(cyclohexylamino)-6-fluoro-1-tetrahydrofuran-3-yl)quinolin-4(1H)-one trifluoroacetate was obtained.


Example 48

To a 4.8 ml DMSO solution of 240 mg of 7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-3-(3-hydroxypropyl)quinolin-4(1H)-one were added 300 mg of a sulfur trioxide pyridine complex and 0.8 ml of triethylamine, followed by overnight stirring at room temperature. Water was added to the reaction mixture, followed by extraction with chloroform and then washing with aqueous saturated sodium chloride. After drying over anhydrous sodium sulfate and subsequent evaporation under a reduced pressure, the resulting residue was purified by silica gel column chromatography to obtain 140 mg of an aldehyde compound. To a 2.8 ml DMF solution of 140 mg of the aldehyde compound were added 141 mg of potassium carbonate and 414 mg of ethyl (diethoxyphosphoryl)acetate, followed by overnight stirring at 60° C. The reaction mixture was cooled to room temperature, water was added, and the insoluble materials were collected by filtration. By purifying the resulting insoluble materials by silica gel column chromatography, 57 mg of ethyl (2E)-5-[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]pent-2-enoate was obtained.


Example 49

3 ml of ethyl acetate and 0.35 ml of a 1 M hydrogen chloride ethyl acetate solution were added to 0.13 g of ethyl({[7-(cyclohexylamino)-1-ethyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]methyl}amino)acetate obtained by the same method of Example 9. After evaporation of the solvent under a reduced pressure and subsequent addition of ether, the insoluble materials were collected by filtration to obtain 97 mg of ethyl({[7-(cyclohexylamino)-1-ethyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]methyl}amino)acetate hydrochloride.


Example 50

10 ml of ethyl acetate, 45 mg of oxalic acid and 10 ml of ethanol were added to 440 mg of ethyl({[7-(cyclohexylamino)-6-fluoro-4-oxo-1-(tetrahydrofuran-3-yl)-1,4-dihydroquinolin-3-yl]methyl}amino)acetate obtained by the same method of Example 4. After evaporation of the solvent under a reduced pressure and subsequent addition of ethyl acetate, the insoluble materials were collected by filtration to obtain 349 mg of ethyl({[7-(cyclohexylamino)-6-fluoro-4-oxo-1-(tetrahydrofuran-3-yl)-1,4-dihydroquinolin-3-yl]methyl}amino)acetate oxalate.


Example 51

To 0.25 g of ethyl({[7-(cyclohexylamino)-6-fluoro-4-oxo-1-(tetrahydrofuran-3-yl)-1,4-dihydroquinolin-3-yl]methyl}amino)acetate oxalate were added water and potassium carbonate, followed by extraction with chloroform. After drying over anhydrous sodium sulfate and subsequent filtration, the solvent was evaporated under a reduced pressure. To a 10 ml ethanol solution of the resulting residue was added 0.60 ml of aqueous 1 M sodium hydroxide solution under ice-cooling, followed by stirring under ice-cooling for 1 hour and at room temperature overnight. After evaporation of the solvent under a reduced pressure, water and trifluoroacetic acid were added. By purifying by an ODS column chromatography, 251 mg of ({[7-(cyclohexylamino)-6-fluoro-4-oxo-1-(tetrahydro furan-3-yl)-1,4-dihydroquinolin-3-yl]methyl}amino)acetic acid trifluoroacetate was obtained.


Example 52

To a 2.0 ml chloroform solution of 155 mg of diethyl[2-(acetyl{[7-(cyclohexylamino)-1-(1-ethylpropyl)-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]methyl}amino)-1,1-difluoroethyl]phosphonate was added 0.27 ml of bromotrimethylsilane, followed by overnight stirring at room temperature. The reaction mixture was evaporated under a reduced pressure, and aqueous 1 M sodium hydroxide solution was added to the resulting residue, followed by purification by an ODS column chromatography and washing with ethyl acetate to obtain 100 mg of disodium [2-(acetyl{[7-(cyclohexylamino)-1-(1-ethylpropyl)-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]methyl}amino)-1,1-difluoroethyl]phosphonate.


Example 53

To an 8.0 ml ethanol solution of 280 mg of ethyl (2E)-4-{[7-(cyclohexylamino)-6-fluoro-1-isopropyl-4-oxo-1,4-dihydroquinolin-3-yl]oxy}but-2-enoate was added 28 mg of rhodium-carbon (10%) at room temperature, followed by stirring for 2 hours in an atmosphere of hydrogen. After filtration using celite, the filtrate was evaporated under a reduced pressure, and the residue was purified by silica gel column chromatography to obtain 202 mg of ethyl 4-{[7-(cyclohexylamino)-6-fluoro-1-isopropyl-4-oxo-1,4-dihydroquinolin-3-yl]oxy}butanoate.


Example 54

To a 1.0 ml THF-1.0 ml methanol mixed solution of 130 mg of N-[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]-2-[(4R)-2,2-dimethyl-5-oxo-1,3-dioxolan-4-yl]acetamide was added 0.3 ml of 1 M hydrochloric acid, followed by overnight stirring at room temperature. Then, 0.8 ml of aqueous 1M sodium hydroxide solution was added, followed by overnight stirring at room temperature. The resulting reaction mixture was neutralized with 1 M hydrochloric acid, and then the insoluble materials were collected by filtration and purified by silica gel column chromatography to obtain 11 mg of (2R)-4-{[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]amino}-2-hydroxy-4-oxobutanoic acid.


Example 55

To a 2.0 ml THF solution of 100 mg of (2E)-3-[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]acrylic acid was added 60 mg of 1,1′-carbonyldiimidazole, followed by overnight stirring at room temperature. By adding water to the resulting reaction mixture and collecting the insoluble materials by filtration, an acylimidazole compound was obtained. To a 2.0 ml DMF solution of the resulting acylimidazole compound was added 0.5 ml of aqueous ammonia, followed by overnight stirring at 60° C. The resulting reaction mixture was cooled to room temperature, water was added, and the insoluble materials were collected by filtration to obtain 58 mg of (2E)-3-[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]acrylamide.


Example 56

To a 5.0 ml ethanol solution of 500 mg of 7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carbaldehyde was added 215 mg of ethyl aminoacetate hydrochloride, followed by stirring at room temperature for 2 hours. Next, 50 mg of palladium-carbon was added thereto, followed by stirring at room temperature for 4 hours in an atomosphere of hydrogen. The reaction mixture was filtered through celite and then evaporated under a reduced pressure. The resulting residue was purified by silica gel column chromatography. To a 3.6 ml dioxane solution of the resulting compound was added 4.0 ml of a 4 M hydrogen chloride dioxane solution, followed by overnight stirring at room temperature. The insoluble materials were collected by filtration to obtain 320 mg of ethyl({[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]methyl}amino)acetate hydrochloride.


Example 57

2.0 ml of THF and 0.071 ml of chlorotrimethylsilane were added to 73 mg of zinc, followed by stirring at room temperature for 15 minutes. Then, 200 mg of ethyl (2E)-4-bromobut-2-enoate was added thereto, followed by stirring at room temperature for 30 minutes. To the reaction mixture was added 7-(cyclohexylamino)-1-(1-ethylpropyl)-6-fluoro-4-oxo-1,4-dihydro quinoline-3-carbaldehyde, followed by overnight stirring at room temperature. Water was added to the reaction mixture, followed by extraction with chloroform. The organic layer was washed with aqueous saturated sodium chloride, dried over anhydrous sodium sulfate and then evaporated under a reduced pressure. The resulting residue was purified by silica gel column chromatography to obtain 30 mg of ethyl (2E)-5-[7-(cyclohexylamino)-1-(1-ethylpropyl)-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]-5-hydroxypent-2-enoate.


Example 58

To a 5 ml THF solution of 119 mg of 60% sodium hydride was added 598 μl of ethyl(diethoxyphosphoryl)acetate at 0° C., followed by stirring for 30 minutes. A 5 ml THF solution of 400 mg of 7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-3-(2-oxopropoxy)quinolin-4(1H)-one was added thereto at the same temperature, followed by stirring at room temperature for 2 hours. To the reaction mixture was added aqueous saturated ammonium chloride, followed by extraction with ethyl acetate. The organic layer was washed with aqueous saturated sodium chloride, dried over anhydrous sodium sulfate, and concentrated under a reduced pressure. The resulting residue was purified by silica gel column chromatography to obtain 200 mg of ethyl (2E)-4-{[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]oxy}-3-methylbut-2-enoate.


Example 59

To a 20 ml THF suspension of 1081 mg of (3-benzyloxypropyl)triphenylphosphonium bromide was added 258 mg of potassium, tert-butoxide followed by stirring for 1.5 hours. A 10 ml THF solution of 358 mg of 7-(cyclohexylamino)-1-(1-ethylpropyl)-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carbaldehyde was added thereto, followed by stirring for 1 hour. To the reaction mixture was added aqueous saturated ammonium chloride, followed by extraction with ethyl acetate and washing with aqueous saturated sodium chloride. After drying over anhydrous sodium sulfate and subsequent concentration under a reduced pressure, the residue was purified by silica gel column chromatography to obtain 488 mg of 3-[4-(benzyloxy)but-1-en-1-yl]-7-(cyclohexylamino)-1-(1-ethylpropyl)-6-fluoroquinolin-4(1H)-one.


Example 60

To a 2 ml dichloromethane solution of 100 mg of 5-chlorothiophene-2-carboxylic acid was added 0.55 ml of chlorosulfonyl isocyanate, followed by overnight stirring at 40° C. The solvent was evaporated under a reduced pressure, and the resulting residue was dissolved in 1.5 ml of dichloromethane. Then, 150 mg of 3-amino-7-(cyclohexylamino)-1-cyclopentyl-6-fluoroquinolin-4(1H)-one and 0.91 ml of triethylamine was added, followed by overnight stirring at room temperature. Water was added to the reaction mixture, followed by extraction with chloroform. The organic layer was washed with aqueous saturated sodium chloride. After drying over anhydrous sodium sulfate and subsequent filtration, the solvent was evaporated under a reduced pressure. The resulting residue was purified by silica gel column chromatography to obtain 64 mg of 5-chloro-N-({[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]amino}sulfonyl)thiophene-2-carboxamide.


Example 61

To a 6 ml DMSO suspension of 200 mg of 60% sodium hydride was added 1.1 g of trimethylsulfoxonium iodide, followed by stirring for 30 minutes. To the reaction mixture was added 242 mg of ethyl (2E)-3-[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]acrylate, followed by stirring at room temperature for 1 hour and at 60° C. for 1 hour. To the reaction mixture was added water, followed by extraction with diethyl ether. The organic layer was washed with aqueous saturated sodium chloride. After drying over anhydrous sodium sulfate, the solvent was evaporated under a reduced pressure. The resulting residue was purified by silica gel column chromatography to obtain 55 mg of ethyl 2-[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]cyclopropanecarboxylate.


Example 62

To a 30 ml methanol solution of 1.5 g of {[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]oxy}acetonitrile were added 1.1 ml of triethylamine and 540 mg of hydroxylamine hydrochloride, followed by heating under reflux for 27 hours. The solvent was evaporated under a reduced pressure, and the resulting residue was purified by silica gel column chromatography to obtain 850 mg of 2-{[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]oxy}-N′-hydroxyethanimidamide.


Example 63

40 μl of diketene was added dropwise under ice-cooling to a 8 ml chloroform solution of 800 mg of 2-{[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]oxy}-N′-hydroxyethanimidamide, followed by stirring under ice-cooling for 6 hours. By evaporating the solvent under a reduced pressure, 180 mg of N′-(acetoacetyloxy)-2-{[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]oxy}ethanimidamide was obtained.


Example 64 and Example 65

5 ml of toluene and 41 mg of 60% sodium hydride were added to 180 mg of N′-(acetoacetyloxy)-2-{[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3yl]oxy}ethanimidamide, followed by heating under reflux for 24 hours. The solvent was evaporated under a reduced pressure, and dilute hydrochloric acid was added to the resulting residue, followed by extraction with ethyl acetate and washing with water and aqueous saturated sodium chloride. After drying over anhydrous sodium sulfate, the solvent was evaporated under a reduced pressure, and the resulting residue was purified by silica gel column chromatography to obtain 10 mg of 7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-3-[(5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)methoxy]quinolin-4(1H)-one (Example 64) and 30 mg of 7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-3-{[5-(2-oxopropyl)-1,2,4-oxadiazol-3-yl]methoxy} quinolin-4(1H)-one (Example 65).


Example 66

0.14 ml of N-(chlorocarbonyl) isocyanate was added dropwise at −50° C. to a 4 ml THF solution of 110 mg of 7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-3-[(hydroxyamino)methyl]quinolin-4(1H)-one, followed by stirring at room temperature for 1 hour. 1 M hydrochloric acid was added to the reaction mixture, followed by extraction with chloroform and washing with aqueous saturated sodium chloride. After drying over anhydrous sodium sulfate, the solvent was evaporated under a reduced pressure, and the resulting residue was purified by silica gel column chromatography to obtain 45 mg of 2-{[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]methyl}-1,2,4-oxadiazolidine-3,5-dione.


Example 67

To a 4 ml DMSO solution of 310 mg of 7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-3-(4-hydroxybutyl)quinolin-4(1H)-one was added 0.7 ml of triethylamine and 620 mg of a sulfur trioxide pyridine complex, followed by stirring at room temperature for 24 hours. By adding 1 M hydrochloric acid and water, the insoluble materials were collected by filtration to obtain 290 mg of 4-[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]butanal.


Example 68

To 285 mg of 4-[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]butanal were added 9 ml of toluene and 250 mg of methyl (triphenylphosphoranilidene)acetate, followed by stirring at 80° C. for 14 hours. The solvent was evaporated under a reduced pressure, and the resulting residue was purified by silica gel column chromatography to obtain 260 mg of methyl (2E)-6-[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]hex-2-enoate.


Example 69

To 500 mg of 7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carbaldehyde were added 5 ml of ethanol, 460 mg of sodium acetate and 290 mg of hydroxylamine hydrochloride, followed by stirring at room temperature for 15 hours and at 70° C. for 12 hours. The solvent was evaporated under a reduced pressure, and water was added to the resulting residue, followed by extraction with chloroform and washing with aqueous saturated sodium chloride. After drying over anhydrous sodium sulfate, the solvent was evaporated under a reduced pressure to obtain 300 mg of 7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carbaldehyde oxime.


Example 70

15 ml of methanol, 15 ml of THF and 250 mg of sodium cyanoborohydride were added to 300 mg of 7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carbaldehyde oxime. 2 ml of a 4 M hydrogen chloride dioxane solution was added thereto under ice-cooling, followed by stirring at room temperature for 3 hours. Under ice-cooling, aqueous 1 M sodium hydroxide solution was added thereto, followed by extraction with chloroform and subsequent washing with aqueous saturated sodium chloride. After drying over anhydrous sodium sulfate, the solvent was evaporated under a reduced pressure, and the resulting residue was purified by silica gel column chromatography to obtain 130 mg of 7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-3-[(hydroxyamino)methyl]quinolin-4(1H)-one.


Example 71

To a 50 ml THF suspension of 1.02 g of 9-(cyclohexylamino)-8-fluoro-6-oxo-2,3,4,6-tetrahydro-1H-pyrido[1,2-a]quinoline-5-carboxylic acid were added 0.5 ml of triethylamine and 0.4 ml of isobutyl chloroformate under ice-cooling, followed by stirring under ice-cooling for 1 hour. Aqueous solution (4 ml) of 431 mg of sodium borohydride was added dropwise thereto at −78° C., followed by stirring at −15° C. for 15 minutes and under ice-cooling for 30 minute. Aqueous saturated ammonium chloride was added thereto, followed by extraction with ethyl acetate and subsequent drying over anhydrous sodium sulfate. The solvent was evaporated under a reduced pressure, and the resulting residue was purified by silica gel column chromatography to obtain 495 mg of 9-(cyclohexylamino)-8-fluoro-5-(hydroxymethyl)-1,2,3,4-tetrahydro-6H-pyrido[1,2-a]quinolin-6-one.


In the same manner as in the above-mentioned Examples 1 to 71, Example compounds shown in the following Tables 10 to 73 were produced using respectively corresponding starting materials. MS data of the example compounds are shown in the following Tables 10 to 73, and NMR data of several Example compounds in Tables 74 and 75.


Structures of other compounds of the present invention are shown in Tables 76 to 83. These may be easily produced by the use of the above-mentioned production methods, and the methods described in examples or the methods obvious to those skilled in the art, or modified methods thereof.









TABLE 4









embedded image
















Rf
RSyn
R4
R
Data














11
1
Et
—C(O)NH2
FAB: 332


12
1
—CH(Et)2
—C(O)NH2
FAB: 374


1
1
cPen
—C(O)NH2
FAB: 372





13
1


embedded image


—C(O)NH2
FAB: 374





14
1


embedded image


—C(O)NH2
FAB: 473





2
2
cPen
—C(O)N(Me)—OMe
FAB: 416





15
9, E37


embedded image


—CO2H
ESI: 387





16
E37, E2


embedded image


—CO2H
FAB: 401
















TABLE 5









embedded image















Rf
RSyn
R4
Data





10
10


embedded image


ESI: 336





17
10


embedded image


FAB: 350
















TABLE 6









embedded image

















Rf
RSyn
R4
Data
















18
3
iPr
FAB: 269



19
3
—CH(Et)2
ESI: 297



3
3
cPen
FAB: 295







20
3


embedded image


FAB: 321







21
3


embedded image


FAB: 341




















TABLE 7





Rf
RSyn
Structure
Data


















4
4


embedded image


EI: 215





5
5


embedded image


FAB: 386





22
4


embedded image


ESI: 180
















TABLE 8









embedded image



















Rf
RSyn
X
R′
R2
R3
R
Data

















6
6
CH
F
F
F
—CO2Et
FAB: 340


23
9
N
Cl
F
H
—CO2H
FAB: 311


24
5, 6
CH
F
H
H
—CO2Et
FAB: 304


9
9
CH
F
H
H
—CO2H
FAB: 276
















TABLE 9









embedded image



















Rf
RSyn
X
R2
R3
Data

















7
7
CH
F
F
FAB: 391



8
8
CH
F
—OBn
FAB: 479



25
E37
N
F
H
FAB: 374



26
E37
CH
H
H
FAB: 355
















TABLE 10









embedded image















Ex
Syn
Rb
Data













72
40
H
FAB: 319


27
27
—CH2CO2Et
FAB: 405


73
2
—CH2CO2H
FAB: 377





74
27


embedded image


ESI: 431





75
2


embedded image


FAB: 403





53
53
—(CH2)3CO2Et
FAB: 433


76
2
—(CH2)3CO2H
FAB: 405


77
46
—CH(Me)C(O)NH—S(O)2Me
FAB(Neg): 466


78
46
—CH(Me)C(O)NH—S(O)2Ph
FAB: 530





79
12


embedded image


FAB: 477





80
2


embedded image


FAB: 449





81
12


embedded image


FAB: 405





82
2


embedded image


FAB: 391





83
Rfl


embedded image


FAB: 390





84
12


embedded image


ESI: 461





85
2


embedded image


FAB: 433





















TABLE 11









86
12


embedded image


FAB: 557







87
2


embedded image


ESI: 467







88
27


embedded image


FAB: 445







89
2


embedded image


FAB: 417

















TABLE 12









embedded image
















Ex
Syn
R3
Rb
Data














90
40
F
H
FAB: 365


91
27

—CH2CO2Et
FAB: 451


92
2

—CH2CO2H
FAB: 518


93
40
H
H
FAB: 347


94
27

—CH2CO2Et
FAB: 433


95
2

—CH2CO2H
FAB: 405





96
27



embedded image


FAB: 459





97
27

—(CH2)3—P(O)(OEt)2
FAB: 525


98
18

—(CH2)3—PO3H2
FAB: 469





99
12



embedded image


FAB: 433





100
2



embedded image


FAB: 419
















TABLE 13









embedded image

















Ex
Syn
Rb
Data















40
40
H
FAB: 345



101
27
—CH2CO2Et
FAB: 431



102
2
—CH2CO2H
FAB: 403



103
27
—C(Me)2CO2Et
FAB: 459



104
2
—C(Me)2CO2H
FAB: 431



105
11
—(CH2)3CO2Et
FAB: 459



106
2
—(CH2)3CO2H
FAB: 431






107
27


embedded image


FAB: 457






108
2


embedded image


FAB: 429






109
24


embedded image


FAB: 519






110
11
—CH2CH(Ph)CH2CO2Me
FAB: 521



111
2
—CH2CH(Ph)CH2CO2H
FAB: 507






112
12


embedded image


FAB: 583






113
2


embedded image


FAB: 493






12
12


embedded image


FAB: 583






114
2


embedded image


FAB: 493






115
12


embedded image


FAB: 507






116
2


embedded image


FAB: 479






117
13


embedded image


FAB: 446





















TABLE 14









118
14


embedded image


FAB: 465







14
14


embedded image


FAB: 465







13
13


embedded image


FAB: 446







119
27
—CH2C(O)Ph
FAB: 463



120
12
—(CH2)3—OTBDMS
FAB: 517



121
27
—(CH2)2—OH
FAB: 389



42
42
—(CH2)3—OH
ESI: 403







122
12


embedded image


FAB: 535







123
2


embedded image


FAB: 507







124
12


embedded image


FAB: 431







125
2


embedded image


FAB: 417







126
27


embedded image


FAB: 459







127
2


embedded image


FAB: 431







128
12


embedded image


FAB: 431







129
2


embedded image


FAB: 417







130
12


embedded image


FAB: 487







131
2


embedded image


FAB: 459







132
12


embedded image


FAB: 499







133
2


embedded image


FAB: 485






















TABLE 15









134
12


embedded image


FAB: 457







135
2


embedded image


ACPI: 443







136
53


embedded image


FAB: 459







137
2


embedded image


FAB: 445







138
12


embedded image


FAB: 503







139
2


embedded image


FAB: 475







140
27
—CH2CN
FAB: 384







32
32


embedded image


FAB: 427







141
2


embedded image


FAB: 443







142
27


embedded image


FAB: 401







58
58


embedded image


FAB: 471







143
53


embedded image


FAB: 445







144
2


embedded image


FAB: 445







145
12
—(CH2)4—CO2Me
FAB: 459



146
2
—(CH2)4—CO2H
FAB: 445







147
12


embedded image


FAB: 471







148
2


embedded image


FAB: 443







149
53


embedded image


FAB: 445





















TABLE 16








62
62


embedded image


FAB: 417






63
63


embedded image


FAB: 501






64
64


embedded image


FAB: 443






65
65


embedded image


FAB: 483






150
27


embedded image


FAB: 493






151
2


embedded image


FAB: 479
















TABLE 17









embedded image
















Ex
Syn
R4
Rb
Data





152 153 154
40 27 2


embedded image


H —CH2CO2Et —CH2CO2H
FAB: 371 FAB: 457 FAB: 429





155 156 157
40 27 2


embedded image


H —CH2CO2Et —CH2CO2H
FAB: 359 FAB:: 445 FAB: 417





158
40
—CH2CF3
H
FAB: 359


159
27

—CH2CO2Et
ESI: 445


160
2

—CH2CO2H
FAB: 417


161 162 163
40 27 2


embedded image


H —CH2CO2Et —CH2CO2H
FAB: 373 FAB:: 459 FAB: 431
















TABLE 18









embedded image

















Ex
Syn
Rb
Data
















164
40
H
FAB: 363







165
12


embedded image


FAB: 449







166
2


embedded image


FAB: 435

















TABLE 19









embedded image

















Ex
Syn
Rb
Data
















167
40
H
ESI: 327







168
2


embedded image


FAB: 399







169
2


embedded image


FAB: 413







170
12


embedded image


FAB: 413







171
12


embedded image


ESI: 427

















TABLE 20









embedded image
















Ex
Syn
R4
R5
Data





172
37
iPr
—NO2
ESI: 320


173
11

—NH2
ESI: 290


174
37
—CH(Et)2
—NO2
ESI: 348


175
11

—NH2
ESI: 318


176
37
cPen
—NO2
FAB: 346


177
11

—NH2
ESI: 316
















TABLE 21









embedded image
















Ex
Syn
R4
R5
Data














178
37
iPr
—NO2
ESI: 348


179
11

—NH2
ESI: 318


180
37
—CH(Et)2
—NO2
FAB: 376


181
11

—NH2
FAB: 346


38
38

—NHMe
FAB: 360


182
9

—NHCH2CO2Et
FAB: 432


183
2

—NHCH2CO2H
ESI: 404


45
45

—N(Bn)CH2CO2Et
FAB: 522


184
2

—N(Bn)CH2CO2H
ESI: 494


185
10

—N(Bz)CH2CO2Et
FAB: 536


186
2

—N(Bz)CH2CO2H
FAB: 508





187
5



embedded image


ESI: 514





37
37
cPen
—NO2
FAB: 374


188
11

—NH2
FAB: 314





189
9,2



embedded image


ESI: 416





60
60



embedded image


ESI(neg): 565





190 191
37 11


embedded image


—NO2 —NH2
FAB: 400 FAB: 370





192 193
37 11


embedded image


—NO2 —NH2
FAB: 420 FAB: 390
















TABLE 22









embedded image
















Ex
Syn
R1
R4
Data














194
8
cPr—CH2
iPr
FAB: 513


195
8

cPen
ESI: 539


8
8
cHex
iPr
ESI: 541


196
8

—CH(Et)2
FAB: 569


197
8

cPen
FAB: 567
















TABLE 23









embedded image
















Ex
Syn
R4
Re
Data














198
8
iPr
—SO2—Ph
FAB: 501


199
8

—SO2—Me
FAB: 439





200
8



embedded image


FAB: 535





7
7
—CH(Et)2
—(CH2)2—CO2Et
FAB: 489


201
2

—(CH2)2—CO2H
ESI: 461


202
7
cPen
—(CH2)2—CO2H
ESI: 459


203
2

—(CH2)2—CO2Et
FAB: 487





204
7



embedded image


FAB: 521





205
2



embedded image


FAB: 507





206
7

—CH(Me)CH2CO2Et
FAB: 501


207
2

—CH(Me)CH2CO2H
FAB: 473
















TABLE 24









embedded image
















Ex
Syn
R6
Rd
Data














208
1
Me
—(CH2)2—CO2Et
FAB: 488


209
2

—(CH2)2—CO2H
FAB: 460


10
10
—CH2CO2Et
—(CH2)3—CO2Et
FAB: 574


210
2
—CH2CO2H
—(CH2)3—CO2H
FAB: 518
















TABLE 25









embedded image
















Ex
Syn
R4
Rd
Data





211
1
iPr
—(CH2)3—CO2Et
FAB: 432


212
2

—(CH2)3—CO2H
FAB: 404


213
1
—CH(Et)2
—(CH2)3—CO2Et
FAB: 460


214
2

—(CH2)3—CO2H
FAB: 432


215
1
cPen
—(CH2)3—CO2Et
ESI: 458


216
2

—(CH2)3—CO2H
FAB: 430





217
1



embedded image


FAB: 478





218
2



embedded image


FAB: 492
















TABLE 26









embedded image
















Ex
Syn
R4
Rd
Data





219
1
iPr
—(CH2)2—CO2Et
FAB: 446


220
2

—(CH2)2—CO2H
FAB: 418


221
1

—(CH2)3—CO2Et
FAB: 460


222
2

—(CH2)3—CO2H
FAB: 432


223
1

—(CH2)3—CO2—(CH2)2—NMe2
FAB: 503





224
2



embedded image


FAB: 460





225
1



embedded image


FAB: 446





226 227
2 1


embedded image


—(CH2)3—CO2Et —(CH2)3—CO2H
FAB: 512 FAB: 484





228 229
2 1


embedded image


—(CH2)3—CO2Et —(CH2)3—CO2H
FAB: 532 FAB: 504
















TABLE 27









embedded image

















Ex
Syn
Rd
Data
















230
1
—CH2CO2Et
FAB: 460



231
2
—CH2CO2H
FAB: 432



232
1
—(CH2)2CO2Et
FAB: 474



233
2
—(CH2)2CO2H
FAB: 446



234
1
—(CH2)3CO2Et
FAB: 488



235
2
—(CH2)3CO2H
FAB: 460



236
1, 2
—(CH2)4—CO2H
FAB: 474







237
2


embedded image


FAB: 474







238
1


embedded image


FAB: 460



239
2
—CH(Et)CO2Et
FAB: 488



240
1
—CH(Et)CO2H
FAB: 460



241
2
—C(Me)2CO2Et
FAB: 488



242
1
—C(Me)2CO2H
FAB: 460







243
2


embedded image


FAB: 488







244
1


embedded image


FAB: 474







245
2
—CH2CH(Me)CH2CO2Me
FAB: 488



246
1
—CH2CH(Me)CH2CO2H
FAB: 474







30
30


embedded image


FAB: 500







247
11
—CH(Et)—(CH2)2—CO2Me
FAB: 502



248
2
—CH(Et)—(CH2)2—CO2H
FAB: 488







249
1


embedded image


FAB: 458






















TABLE 28









250
1


embedded image


FAB: 458







251
2


embedded image


FAB: 476







252
2


embedded image


FAB: 476







253
1
—(CH2)2—CH(Ph)CO2Et
ESI: 564



254
2
—(CH2)2—CH(Ph)CO2H
ESI: 536



255
2
—CH2CH(Ph)CH2CO2H
FAB: 536



256
1
—CH2CH(Ph)CH2CO2Et
FAB: 564



257
1
—CH2OCH2CO2Et
ESI: 490



258
2
—CH2OCH2CO2H
FAB: 462







9
9


embedded image


ESI: 575







259
2


embedded image


ESI: 519







260
2
—(CH2)2—P(O)(OEt)2
FAB: 538



261
52
—(CH2)2—PO3Na2
FAB: 482






(M+ − 2Na + 3)



262
1
—CH2NHBoc
FAB: 503



28
28
—CH2NH2
FAB: 403;






Sal: 2HCl



263
29
—CH(Et)CH2OH
FAB: 446







264
2


embedded image


ESI: 498







265
2


embedded image


FAB: 500







266
1


embedded image


FAB: 512






















TABLE 29









267
11


embedded image


ESI: 514







268
1


embedded image


FAB: 594







269
2


embedded image


FAB: 538

















TABLE 30









embedded image

















Ex
Syn
Rd
Data
















1
1
—(CH2)2—CO2Et
FAB: 472



2
2
—(CH2)2—CO2H
FAB: 444



270
1
—(CH2)3—CO2Et
FAB: 486



271
2
—(CH2)3—CO2H
FAB: 458



272
1
—(CH2)4—CO2Et
FAB: 500



273
2
—(CH2)4—CO2H
FAB: 472







274
1


embedded image


FAB: 470







275
2


embedded image


FAB: 442







276
1


embedded image


APCI: 486







277
2


embedded image


FAB: 472







278
1


embedded image


FAB: 500







54
54


embedded image


FAB: 460







279
1
—CH2CH(Ph)CH2CO2Et
FAB: 562



280
2
—CH2CH(Ph)CH2CO2H
FAB: 534



281
1
—(CH2)2—P(O)(OEt)2
FAB: 536



282
3
—(CH2)2—PO3H2
FAB: 480






Sal: HBr







283
1


embedded image


FAB: 506






















TABLE 31









284
2


embedded image


FAB: 492







285
1


embedded image


FAB: 506







286
2


embedded image


FAB: 492







287
1


embedded image


FAB: 592







288
2


embedded image


FAB: 564







289
2


embedded image


FAB: 536







290
10
—CO2Et
FAB: 444



291
2
—CO2H
ESI: 416







292
2


embedded image


FAB: 474







293
1


embedded image


ESI: 544

















TABLE 32









embedded image
















Ex
Syn
R4
R5
Data














294
29
cPen
—CH2OH
FAB: 331


295
39

—CHO
FAB: 329





296
24



embedded image


FAB: 399





297
2



embedded image


ESI: 371





298
29
iPr
—CH2OH
FAB: 305


299
39

—CHO
FAB: 303





300
24



embedded image


FAB: 373





301
2



embedded image


FAB: 345





46
46



embedded image


FAB: 524
















TABLE 33









embedded image
















Ex
Syn
R3
R5
Data














302
29
F
—CH2OH
FAB: 379


303
39

—CHO
FAB: 377





304
24



embedded image


FAB: 447





305
2



embedded image


FAB: 419





306
29
—OBn
—CH2OH
ESI: 467


307
11
—OH
—CH2OH
ESI: 377


308
39

—CHO
FAB (Neg):






373





309
24



embedded image


FAB: 445





310
2



embedded image


FAB: 417





311
2



embedded image


ESI: 532





312
2



embedded image


FAB: 560





313
1



embedded image


FAB: 588





314
24



embedded image


ESI: 509





315
3



embedded image


ESI: 453 Sal: HBr
















TABLE 34









embedded image
















Ex
Syn
R4
R5
Data














316
29
Et
—CH2OH
FAB: 319


317
39

—CHO
FAB: 317


318
29
iPr
—CH2OH
FAB: 333


319
39

—CHO
FAB: 331





320
24



embedded image


FAB: 401





321
2



embedded image


ESI: 373





322
41



embedded image


FAB: 446





323
46



embedded image


FAB: 450





324
46



embedded image


FAB: 512





325
55



embedded image


ESI: 506





326
29


embedded image


—CH2OH
FAB: 361





327 328 329 330
29 39 24 2


embedded image


—CH2OH —CHO embedded imageembedded image
FAB: 361 FAB: 359 FAB: 429 FAB: 401





331 332 333 334
29 39 24 2


embedded image


—CH2OH —CHO embedded imageembedded image
FAB: 361 FAB: 359 FAB: 429 FAB: 401




















TABLE 35







335
28


embedded image


—CH2OH
FAB: 360 Sal: 2HCl





336
5


embedded image


—CH2OH
FAB: 374





337
29


embedded image


—CH2OH
FAB: 460





338
29


embedded image


—CH2OH
FAB: 438





339
29


embedded image


—CH2OH
FAB: 388





340
29
—CH(Me)(cBu)
—CH2OH
FAB: 373


341
39

—CHO
FAB: 371


342
29
—CH2CF3
—CH2OH
FAB: 373


343
39

—CHO
FAB: 371





344 345
29 39


embedded image


—CH2OH —CHO
FAB: 387 FAB: 385





346 347
29 39


embedded image


—CH2OH —CHO
FAB: 385 FAB: 383
















TABLE 36









embedded image















Ex
Syn
R5
Data













348
29
—CH2OH
FAB: 361


349
39
—CHO
FAB: 359


350
11
—(CH2)4—OH
FAB: 403





351
6


embedded image


ESI(Neg): 427





352
29


embedded image


ESI: 387





59
59


embedded image


FAB: 491





353
24


embedded image


FAB: 429





354
2


embedded image


FAB: 401





355
11
—(CH2)2—CO2Et
FAB: 431


356
2
—(CH2)2—CO2H
FAB: 403





357
24


embedded image


ESI(Neg): 445





358
2


embedded image


FAB: 419





359
24


embedded image


ESI(Neg): 461





360
2


embedded image


FAB: 435





57
57


embedded image


ESI: 473





361
2


embedded image


FAB: 445





362
1


embedded image


FAB: 486





363
2


embedded image


FAB:458



















TABLE 37







364
1


embedded image


FAB: 572





365
2


embedded image


ESI: 544





366
2


embedded image


FAB: 516





367
11


embedded image


FAB: 574





368
2


embedded image


ESI(Neg): 516





369
11
—(CH2)2—P(O)(OEt)2
FAB: 495


370
18
—(CH2)2—PO3H2
FAB: 439


21
21
—(CH2)4—Br
FAB: 465


22
22
—(CH2)4—P(O)(OEt)2
FAB: 523


371
18
—(CH2)4—PO3H2
FAB: 467





Sal: HCl


44
44
—CH(OH)P(O)(OEt)2
FAB: 497


372
18
—CH(OH)PO3H2
FAB: 441


23
23
—CH(OH)CF2P(O)(OEt)2
ESI(Neg): 545


373
18
—CH(OH)CF2PO3H2
FAB: 491





374
24


embedded image


FAB: 493





3
3


embedded image


FAB: 437 Sal: HBr





18
18


embedded image


FAB: 437
















TABLE 38









embedded image
















Ex
Syn
Rpa
Rpb
Data














375
26
H
—CH2OC(O)OiPr
FAB: 553


26
26
H
—CH2OC(O)OtBu
FAB(Neg): 549


25
25
—CH2OC(O)OtBu
—CH2OC(O)OtBu
FAB: 665


376
25
—CH(Me)OC(O)-cHex
—CH(Me)OC(O)-cHex
ESI: 777


377
25
—CH(Me)OC(O)-tBu
—CH(Me)OC(O)-tBu
FAB: 693
















TABLE 39









embedded image

















Ex
Syn
R5
Data
















29
29
—CH2OH
FAB:
359



39
39
—CHO
FAB:
357



19
19
—(CH2)2—OH
FAB:
373



31
31
—(CH2)3—OH
FAB:
387



43
43
Ac
FAB:
371



378
2
—(CH2)2—CO2H
FAB:
401



16
16
—CH(OH)CO2Me
FAB:
417



15
15
—CH(OH)CO2H
FAB:
403



17
17
—CH(CO2Me)—OCH2CO2Et
FAB:
503



379
2
—CH(CO2H)—OCH2CO2H
FAB:
461



20
20
—CH2CO2H
FAB:
387



11
11
—(CH2)2—CO2Et
FAB:
429






24
24


embedded image


FAB:
427






380
2


embedded image


FAB:
399






55
55


embedded image


FAB:
398






381
57, 2


embedded image


ESI:
413






382
24


embedded image


FAB:
441






383
2


embedded image


FAB:
413






384
24


embedded image


FAB:
455






385
2


embedded image


FAB:
427






386
24


embedded image


FAB:
441





















TABLE 40








387
2


embedded image


FAB:
469






388
24


embedded image


FAB:
517






389
2


embedded image


FAB:
489






390
24


embedded image


FAB:
445






391
2


embedded image


FAB:
417






392
24


embedded image


FAB:
461






393
2


embedded image


ESI:
433






48
48


embedded image


FAB:
455






394
2


embedded image


ESI:
427






395
1


embedded image


FAB:
570






396
2


embedded image


ESI:
514






397
24


embedded image


FAB:
491






398
3


embedded image


ESI: Sal:
435 HBr






41
41


embedded image


FAB:
472



















TABLE 41







399
1


embedded image


FAB: 504





400
11


embedded image


FAB: 416





401
55


embedded image


FAB: 414





61
61


embedded image


FAB: 441





402
2


embedded image


FAB: 413





403
41


embedded image


ESI: 456





404
11


embedded image


FAB: 458





69
69


embedded image


FAB: 372





70
70
—CH2NH2OH
FAB:





374





66
66


embedded image


FAB: 443





405
59


embedded image


FAB: 489





406
11
—(CH2)4—OH
FAB:





401


67
67
—(CH2)3—CHO
ESI:





399





68
68


embedded image


FAB: 455





407
2


embedded image


ESI: 441




















TABLE 42








408
24


embedded image


FAB: 380






409
32


embedded image


FAB: 423
















TABLE 43









embedded image



















Ex
Syn
R5
Data


















410
29
—CH2OH
FAB: 377




411
39
—CHO
FAB: 375








412
24


embedded image


FAB: 445








413
2


embedded image


FAB: 417

















TABLE 44









embedded image
















Ex
Syn
R3
R5
Data















414
29
—OBn
—CH2OH
FAB:
465


415
11
—OH
—CH2OH
FAB:
375


416
39
—OH
—CHO
FAB:
373





417
24
—OH


embedded image


FAB:
443





418
2
—OH


embedded image


ESI:
415
















TABLE 45









embedded image



















Ex
Syn
R5
Data


















419
29
—CH2OH
FAB: 341




420
39
—CHO
FAB: 339








421
24


embedded image


FAB: 409








422
2


embedded image


FAB: 381

















TABLE 46









embedded image
















Ex
Syn
R4
R5
Data















423
33
Et
CN
FAB:
314


424
34

—CH2NHBoc
FAB:
418


425
33
—CH(Et)2
CN
FAB:
356


 35
35

—CH2NHBoc
FAB:
460





426
 4



embedded image


FAB:
528





427
 2



embedded image


FAB:
500





428
 8



embedded image


FAB:
583





 33
33
cPen
CN
FAB:
354


 34
34

—CH2NHBoc
FAB:
458





429
 1



embedded image


FAB:
456





430 431
33 34


embedded image


CN —CH2NHBoc
FAB: FAB:
356 460





432
33


embedded image


CN
FAB:
455





433
28


embedded image


CN
FAB: Sal:
355 2HCl





434 435
 5 35


embedded image


CN —CH2NHBoc
FAB: FAB:
369 473
















TABLE 47









embedded image















Ex
Syn
Rc
Data














436
28
H
FAB:
360;





Sal:
2HCl


437
9
—CH2CO2Et
FAB:
446


438
2
—CH2CO2H
FAB:
418


439
4
—(CH2)3—CO2Et
FAB:
474


440
2
—(CH2)3—CO2H
ESI (Neg):
444





441
4


embedded image


FAB:
518





442
2


embedded image


FAB: Sal:
490; AcOH





5
5
—CH(Me)CH2P(O)(OEt)2
ESI:
538


443
3
—CH(Me)CH2PO3H2
ESI:
482;





Sal:
2HBr


444
4, 49
—CH2CF2P(O)(OEt)2
FAB:
560;





Sal:
HCl


445
3
—CH2CF2PO3H2
FAB:
504;





Sal:
HBr
















TABLE 48









embedded image
















Ex
Syn
R4
Rc
Data















446 
28 
Et
H
FAB:
318;






Sal:
2HCl


49
9, 49

—CH2CO2Et
FAB:
404;






Sal:
HCl


447 
2

—CH2CO2H
FAB:
376;






Sal:
HCl





448 
4
iPr


embedded image


FAB:
466





449 
2



embedded image


FAB:
452





450 
28 
cPen
H
FAB:
358;






Sal:
2HCl


56
56 

—CH2CO2Et
FAB:
444;






Sal:
HCl





4
4



embedded image


FAB:
450





451 
4



embedded image


FAB:
450





452 
4



embedded image


FAB:
492





453 
2



embedded image


FAB:
478





47   454  50   51
47    4 4, 50   51 


embedded image


H   —(CH2)3—OH —CH2CO2Et   —CH2CO2H
FAB: Sal: FAB: FAB: Sal: FAB: Sal:
360; TFA 418 418; Oxa 418; TFA





36
36 


embedded image


H
ESI: Sal:
359; 2HCl





455 
28 


embedded image


H
FAB: Sal:
373; 3HCl
















TABLE 49









embedded image

















Ex
Syn
R4
R6
Rc
Data
















456
2
Et
Me
—CH2CO2H
FAB:
390


457
4, 49


—CH2CO2Et
FAB:
418







Sal:
HCl


458
5, 49
—CH(Et)2
Me
—CH2CF2P(O)(OEt)2
FAB:
574







Sal:
HCl


459
52 

Me
—CH2CF2PO3Na2
ESI:
518 (M+ − 2Na + 3)


460
9, 49

—CH2CO2Et
—CH2CO2Et
FAB:
532







Sal:
HCl


461
2

—CH2CO2H
—CH2CO2H
FAB:
476
















TABLE 50









embedded image
















Ex
Syn
R6
Rd
Data





462
10 
—CH2CO2Et
Ph
FAB: 548


463
2
—CH2CO2H

FAB: 520





464 465
10  2
—CH2CO2Et —CH2CO2H


embedded image


FAB: 564 FAB: 536





466
1
—CH2CO2Et


embedded image


FAB: 654





467 468
11  2
  —CH2CO2H


embedded image


FAB: 564 FAB: 536
















TABLE 51









embedded image
















Ex
Syn
R6
Rd
Data















52
52
—CH2CF2PO3Na2
Me
ESI:
546 (M+ − 2Na + 3)


469
6
—CH2CF2P(O)(OEt)2

FAB:
602


6
6
—(CH2)3—CO2Et

FAB:
516


470
2
—(CH2)3—CO2H

FAB:
488


471
10
—CH2CO2Et
—(CH2)2—CO2Et
ESI:
574


472
2
—CH2CO2H
—(CH2)2CO2H
FAB:
518
















TABLE 52









embedded image
















Ex
Syn
R4
Rd
Data















473
10 
Et
—(CH2)2—CO2Et
FAB:
446


474
2

—(CH2)2—CO2H
FAB:
418


475
1

—CH2P(O)(OEt)2
FAB:
496


476
18 

—CH2PO3H2
ESI:
440





477
1



embedded image


FAB:
437





478
10 
—CH(Et)2
—(CH2)2—CO2Et
FAB:
488


479
2

—(CH2)2—CO2H
FAB:
460





480
10, 9



embedded image


ESI:
589





481
2



embedded image


FAB (Neg):
531





482
1

—CH2P(O)(OEt)2
FAB:
538


483
18 

—CH2PO3H2
FAB:
482


484
1

—CHFP(O)(OEt)2
FAB:
556


485
18 

—CHFPO3H2
FAB:
500


486
10 

—CF2P(O)(OEt)2
FAB:
574


487
18 

—CF2PO3H2
FAB:
518


488
1
cPen
—CH2OH
FAB:
416


489
10 

—(CH2)2—CO2Et
FAB:
486


490
2

—(CH2)2CO2H
FAB:
458


491
1

—CH2P(O)(OEt)2
FAB:
536


492
18 

—CH2PO3H2
FAB
478






(Neg):






493 494
10  2


embedded image


—(CH2)2—CO2Et —(CH2)2—CO2H
FAB: FAB:
488 460





495 496
10  2


embedded image


—(CH2)2—CO2Et —(CH2)2—CO2H
FAB: FAB:
501 473
















TABLE 53









embedded image

















Ex
Syn
Rd
Data






497
1
—CH(Me)—nPr
ESI: 456



498
1
—C(Me)2—nPr
ESI: 470



499
1
—C(Me)2—nBu
ESI: 484






500
1


embedded image


ESI: 426






501
1
—CH2CF3
ESI: 468



502
1
—CH2CH(Me)CF3
ESI: 496



503
1
—CH2OH
ESI: 416



504
1
—CH2OEt
ESI: 444



505
1
—CH2CN
ESI: 425






506
1


embedded image


ESI: 488






507
1, 2
—(CH2)2—CO2H
ESI: 458



508
1
—(CH2)3—CO2Et
ESI: 500






509
1, 2


embedded image


ESI: 486






510
1, 2


embedded image


ESI: 500






511
1, 2


embedded image


ESI: 514






512
1, 2


embedded image


ESI: 514






513
1, 2


embedded image


ESI: 456






514
1, 2


embedded image


ESI: 550





















TABLE 54









515
1,2


embedded image


ESI: 621







516
1,2


embedded image


ESI: 607







517
1,2


embedded image


ESI: 577







518
1,2


embedded image


ESI: 607







519
1,2


embedded image


ESI: 621







520
1,2


embedded image


ESI: 621







521
1,2


embedded image


ESI: 621







522
1,2


embedded image


ESI: 540







523
1,2


embedded image


ESI: 540







524
1,2


embedded image


ESI: 554




















TABLE 55







525
1,2


embedded image


ESI: 554





526
1,2


embedded image


ESI: 548





527
1,2


embedded image


ESI: 548





528
1,2
—CH(Ph)CH2CO2H
ESI: 534





529
1


embedded image


ESI: 577





530
1,2


embedded image


ESI: 569





531
1,2


embedded image


ESI: 605





532
1


embedded image


ESI: 410





533
1
cBu
ESI: 440


534
1
cPen
ESI: 454


535
1
cHex
ESI: 468





536
1


embedded image


ESI: 452





537
1


embedded image


ESI: 466





538
1


embedded image


ESI: 516





539
1,2


embedded image


ESI: 498




















TABLE 56








540
1


embedded image


ESI: 572






541
1,2


embedded image


ESI: 512






542
1,2


embedded image


ESI: 512






543
1,2


embedded image


ESI: 512






544
1,2


embedded image


ESI: 510






545
1
—CH2-cPen
ESI: 468






546
1


embedded image


ESI: 466






547
1,2


embedded image


ESI: 526






548
1


embedded image


ESI: 476






549
1


embedded image


ESI: 480






550
1


embedded image


ESI: 480






551
1


embedded image


ESI: 478






552
1


embedded image


ESI: 478






553
1


embedded image


ESI: 494



















TABLE 57







554
1


embedded image


ESI: 494





555
1


embedded image


ESI: 508





556
1


embedded image


ESI: 512





557
1


embedded image


ESI: 604





558
1


embedded image


ESI: 550





559
1


embedded image


ESI: 520





560
1


embedded image


ESI: 520





561
1


embedded image


ESI: 505





562
1


embedded image


ESI: 487





563
1


embedded image


ESI: 490





564
1,2


embedded image


ESI: 506





565
1,2


embedded image


ESI: 551



















TABLE 58







566
1


embedded image


ESI: 540





567
1


embedded image


ESI: 574





568
1


embedded image


ESI: 574





569
1


embedded image


ESI: 538





570
1


embedded image


ESI: 556





571
1,2


embedded image


ESI: 582





572
1


embedded image


ESI: 528





573
1


embedded image


ESI: 528





574
1


embedded image


ESI: 542





575
1


embedded image


ESI: 570





576
1


embedded image


ESI: 492





577
1


embedded image


ESI: 506





















TABLE 59









578
1
—(CH2)4—Ph
ESI: 518







579
1


embedded image


ESI: 526







580
1


embedded image


ESI: 528







581
1


embedded image


ESI: 548







582
1


embedded image


ESI: 556







583
1


embedded image


ESI: 566







584
1


embedded image


ESI: 569







585
1


embedded image


ESI: 542







586
1,2


embedded image


ESI: 496







587
1,2


embedded image


ESI: 578







588
1


embedded image


ESI: 456







589
1


embedded image


ESI: 469







590
1


embedded image


ESI: 469






















TABLE 60









591
1


embedded image


ESI: 545







592
1


embedded image


ESI: 549







593
1


embedded image


ESI: 565







594
1


embedded image


ESI: 569







595
1


embedded image


ESI: 623







596
1


embedded image


ESI: 627







597
1


embedded image


ESI: 643







598
1


embedded image


ESI: 452







599
1


embedded image


ESI: 466







600
1


embedded image


ESI: 480







601
1


embedded image


ESI: 630







602
1


embedded image


ESI: 452






















TABLE 61









603
1


embedded image


ESI: 466







604
1


embedded image


ESI: 480







605
1


embedded image


ESI: 542







606
1


embedded image


ESI: 451







607
1


embedded image


ESI: 465







608
1


embedded image


ESI: 479







609
1


embedded image


ESI: 479







610
1


embedded image


ESI: 617







611
1


embedded image


ESI: 575







612
1


embedded image


ESI: 668







613
1,2


embedded image


ESI: 558























TABLE 62










614
1


embedded image


ESI: 580








615
1


embedded image


ESI: 466








616
1


embedded image


ESI: 497








617
1


embedded image


ESI: 576








618
1


embedded image


ESI: 596








619
1


embedded image


ESI: 452








620
1


embedded image


ESI: 453








621
1


embedded image


ESI: 467








622
1


embedded image


ESI: 467








623
1


embedded image


ESI: 545








624
1


embedded image


ESI: 546








625
1


embedded image


ESI: 546























TABLE 63










626
1


embedded image


ESI: 560








627
1


embedded image


ESI: 470








628
1


embedded image


ESI: 463








629
1


embedded image


ESI: 477








630
1


embedded image


ESI: 477








631
1


embedded image


ESI: 497








632
1


embedded image


ESI: 511








633
1


embedded image


ESI: 529








634
1


embedded image


ESI: 569








635
1


embedded image


ESI: 637








636
1


embedded image


ESI: 463








637
1,2


embedded image


ESI: 507








638
1


embedded image


ESI: 464























TABLE 64










639
1


embedded image


ESI: 478








640
1


embedded image


ESI: 479








641
1


embedded image


ESI: 520








642
1


embedded image


ESI: 532








643
1


embedded image


ESI: 546








644
1


embedded image


ESI: 547








645
1


embedded image


ESI: 501








646
1


embedded image


ESI: 515








647
1


embedded image


ESI: 535








648
1


embedded image


ESI: 517








649
1


embedded image


ESI: 531























TABLE 65










650
1


embedded image


ESI: 561








651
1


embedded image


ESI: 515








652
1


embedded image


ESI: 501








653
1


embedded image


ESI: 518








654
1


embedded image


ESI: 502








655
1


embedded image


ESI: 516








656
1


embedded image


ESI: 516








657
1


embedded image


ESI: 506








658
1


embedded image


ESI: 519








659
1


embedded image


ESI: 531








660
1


embedded image


ESI: 513























TABLE 66










661
1


embedded image


ESI: 529








662
1


embedded image


ESI: 543








663
1


embedded image


ESI: 513








664
1


embedded image


ESI: 513








665
1


embedded image


ESI: 530








666
1


embedded image


ESI: 544








667
1


embedded image


ESI: 548








668
1


embedded image


ESI: 546








669
1


embedded image


ESI: 546








670
1


embedded image


ESI: 530























TABLE 67










671
1


embedded image


ESI: 608








672
1


embedded image


ESI: 520








673
1


embedded image


ESI: 689








674
1


embedded image


ESI: 561








675
1


embedded image


ESI: 557








676
1


embedded image


ESI: 468








677
1


embedded image


ESI: 515








678
1


embedded image


ESI: 531








679
1


embedded image


ESI: 545






















TABLE 68









680
1


embedded image


ESI: 529







681
1


embedded image


ESI: 543







682
1


embedded image


ESI: 544







683
1,2


embedded image


ESI: 535







684
1


embedded image


ESI: 478







685
1


embedded image


ESI: 532







686
1


embedded image


ESI: 538







687
1


embedded image


ESI: 579

















TABLE 69









embedded image















Ex
Syn
Rc
Data





688
5


embedded image


ESI: 484





689
5


embedded image


ESI: 484





690
5


embedded image


ESI: 464





691
5


embedded image


ESI: 492





692
5


embedded image


ESI: 522





693
5


embedded image


ESI: 482





694
5,2


embedded image


ESI: 592





695
5


embedded image


ESI: 532





















TABLE 70









696
5


embedded image


ESI: 532







697
5


embedded image


ESI: 531







698
5


embedded image


ESI: 609







699
5,2


embedded image


ESI: 599







700
5,2


embedded image


ESI: 674

















TABLE 71









embedded image

















Ex
Syn
R5
Data
















701
29
—CH2OH
FAB: 360



702
39
—CHO
FAB: 358







703
24


embedded image


FAB: 428







704
2


embedded image


FAB: 400

















TABLE 72









embedded image

















Ex
Syn
R5
Data
















705
29
—CH2OH
FAB: 360



706
39
—CHO
FAB: 358







707
24


embedded image


FAB: 428







708
2


embedded image


FAB: 400

















TABLE 73









embedded image

















Ex
Syn
R5
Data
















709
40
—OH
FAB: 331



710
27
—OCH2CO2Et
FAB: 417



711
2
—OCH2CO2H
FAB: 389



712
71
—CH2OH
FAB: 345



713
39
—CHO
FAB: 343


















TABLE 74





Ex
Data
















32
NMR(DMSO-d6)δ; 1.11-1.48(m, 5H), 1.60-1.68(m, 1H), 1.70-1.84(m, 8H), 1.90-



1.99(m, 2H), 2.08-2.19(m, 2H), 3.48-3.55(m, 1H), 4.98-5.07(m, 1H), 5.45(s, 2H), 6.03-



6.09(m, 1H), 6.72(d, J = 7.4 Hz, 1H), 7.71(d, J = 12.4 Hz, 1H), 7.74(s, 1H)


76
NMR(DMSO-d6)δ; 1.10-1.23(m, 1H), 1.24-1.48(m, 4H), 1.44(d, J = 6.6 Hz, 6H), 1.58-



1.68(m, 1H), 1.70-1.79(m, 2H), 1.86(quintet, J = 6.9 Hz, 2H), 1.91-2.00(m, 2H),



2.41(t, J = 7.4 Hz, 2H), 3.47-3.58(m, 1H), 3.97(t, J = 6.4 Hz, 2H), 4.89-5.02(m, 1H),



5.92(dd, J = 2.2, 8.3 Hz, 1H), 6.71(d, J = 7.3 Hz, 1H), 7.67(d, J = 12.4 Hz, 1H), 7.74(s, 1H),



12.10(s, 1H)


80
NMR(DMSO-d6)δ; 1.10-1.24(m, 1H), 1.26-1.51(m, 10H), 1.60-1.69(m, 1H), 1.71-



1.80(m, 2H), 1.91-2.07(m, 3H), 2.09-2.20(m, 1H), 2.43-2.60(m, 2H), 3.53-3.65(m, 1H),



4.50(dd, J = 4.9, 7.3 Hz, 1H), 5.03-5.15(m, 1H), 6.23(dd, J = 2.2, 8.3 Hz, 1H), 6.81(d, J = 7.2 Hz, 1H),



7.74(d, J = 12.3 Hz, 1H), 8.11(s, 1H)


82
NMR(DMSO-d6)δ; 1.11-1.23(m, 1H), 1.26-1.51(m, 4H), 1.44(d, J = 6.7 Hz, 3H),



1.47(d, J = 6.5 Hz, 3H), 1.48(d, J = 6.5 Hz, 3H), 1.60-1.69(m, 1H), 1.71-1.80(m, 2H), 1.91-



2.00(m, 2H), 3.53-3.64(m, 1H), 4.56(q, J = 6.8 Hz, 1H), 5.02-5.14(m, 1H),



6.23(dd, J = 2.2, 8.3 Hz, 1H), 6.81(d, J = 7.3 Hz, 1H), 7.75(d, J = 12.3 Hz, 1H), 8.08(s, 1H),



15.23(brs, 1H)


87
NMR(DMSO-d6)δ; 1.11-1.46(m, 12H), 1.58-1.67(m, 1H), 1.68-1.77(m, 2H), 1.85-



1.95(m, 2H), 2.92-3.03(m, 1H), 3.46-3.57(m, 1H), 4.62(brs, 1H), 4.84-4.95(m, 1H), 6.16-



6.28(m, 1H), 6.64-6.71(m, 1H), 6.75-6.96(m, 1H), 7.19-7.39(m, 5H), 7.71(d, J = 12.1 Hz, 1H)


95
NMR(DMSO-d6)δ; 0.74(t, J = 7.2 Hz, 6H), 1.12-1.53(m, 5H), 1.58-2.00(m, 9H), 3.52-



3.68(m, 1H), 4.58(s, 2H), 4.67-4.81(m, 1H), 6.08(d, J = 7.8 Hz, 1H), 6.85(d, J = 6.8 Hz, 1H),



7.72(dd, J = 1.1, 12.3 Hz, 1H), 7.97(s, 1H)


106
NMR(DMSO-d6)δ; 1.11-1.23(m, 1H), 1.25-1.48(m, 4H), 1.60-1.68(m, 1H), 1.71-



1.99(m, 12H), 2.09-2.20(m, 2H), 2.40(t, J = 7.3 Hz, 2H), 3.45-3.56(m, 1H), 3.96(t, J = 6.4 Hz, 2H),



4.96-5.05(m, 1H), 5.95(dd, J = 1.9, 8.2 Hz, 1H), 6.70(d, J = 7.3 Hz, 1H), 7.63(s, 1H),



7.66(d, J = 12.5 Hz, 1H), 12.09(s, 1H)


114
NMR(DMSO-d6)δ; 1.11-1.56(m, 8H), 1.59-1.78(m, 7H), 1.88-1.96(m, 2H), 1.97-



2.08(m, 2H), 3.00(dd, J = 10.4, 14.3 Hz, 1H), 3.49-3.58(m, 1H), 4.72(dd, J = 3.4, 10.4 Hz, 1H),



4.96(quintet, J = 7.2 Hz, 1H), 6.32(d, J = 7.3 Hz, 1H), 6.71(d, J = 7.3 Hz, 1H), 6.88(s, 1H), 7.26-



7.41(m, 5H), 7.73(d, J = 12.2 Hz, 1H), 16.29(brs, 1H)


125
NMR(DMSO-d6)δ; 1.12-1.24(m, 1H), 1.26-1.48(m, 4H), 1.43(d, J = 6.8 Hz, 3H), 1.61-



1.69(m, 1H), 1.72-2.00(m, 10H), 2.13-2.25(m, 2H), 3.50-3.61(m, 1H), 4.58(q, J = 6.8 Hz, 1H),



5.12(quintet, J = 6.8 Hz, 1H), 6.22(dd, J = 2.1, 8.2 Hz, 1H), 6.78(d, J = 7.3 Hz, 1H),



7.73(d, J = 12.3 Hz, 1H), 7.92(s, 1H), 14.87(brs, 1H)


146
NMR(DMSO-d6)δ; 1.12-1.24(m, 1H), 1.25-1.48(m, 4H), 1.60-2.02(m, 15H), 2.09-



2.21(m, 2H), 2.25-2.33(m, 2H), 3.45-3.56(m, 1H), 3.95(s, 2H), 5.01(quintet, J = 6.9 Hz, 1H),



5.95(dd, J = 1.9, 8.2 Hz, 1H), 6.70(d, J = 7.3 Hz, 1H), 7.60(s, 1H), 7.67(d, J = 12.5 Hz, 1H), 11.60-



12.40(br, 1H)


196
NMR(DMSO-d6)δ; 0.74(t, J = 7.3 Hz, 6H), 1.10-1.23(m, 1H), 1.24-1.36(m, 2H), 1.37-



1.50(m, 2H), 1.61-1.79(m, 5H), 1.81-1.97(m, 4H), 3.53-3.66(m, 1H), 4.69-4.80(m, 1H),



6.04(d, J = 7.0 Hz, 1H), 6.82(d, J = 7.0 Hz, 1H), 7.29(d, J = 4.0 Hz, 1H), 7.67(d, J = 12.2 Hz, 1H),



7.71(d, J = 4.2 Hz, 1H), 8.55(s, 1H), 8.62(s, 1H), 11.30-11.70(br, 1H)

















TABLE 75







202
NMR(DMSO-d6)δ; 1.12-1.25(m, 1H), 1.26-1.49(m, 4H), 1.60-1.68(m, 1H), 1.71-



1.89(m, 10H), 1.93-2.01(m, 2H), 2.13-2.26(m, 2H), 2.39(t, J = 6.5 Hz, 2H), 3.47-3.56(m, 1H),



5.05-5.13(m, 1H), 5.93(d, J = 6.2 Hz, 1H), 6.72(d, J = 7.3 Hz, 1H), 7.14(t, J = 5.7 Hz, 1H),



7.67(d, J = 12.4 Hz, 1H), 8.07(s, 1H), 8.92(s, 1H), 12.19(brs, 1H)


233
NMR(DMSO-d6)δ; 0.75(t, J = 7.3 Hz, 6H), 1.11-1.51(m, 5H), 1.61-1.79(m, 5H), 1.81-



1.99(m, 4H), 2.68(t, J = 6.7 Hz, 2H), 3.53-3.64(m, 1H), 4.68-4.78(m, 1H), 5.98(d, J = 6.8 Hz, 1H),



6.82(d, J = 7.2 Hz, 1H), 7.70(d, J = 12.2 Hz, 1H), 8.91(s, 1H), 9.15(s, 1H), 12.09(brs, 1H)


261
NMR(CD3OD)δ; 0.84(t, J = 7.3 Hz, 6H), 1.26-1.41(m, 3H), 1.44-1.58(m, 2H), 1.66-



1.76(m, 1H), 1.79-2.02(m, 8H), 2.04-2.13(m, 2H), 2.69-2.79(m, 2H), 3.46-3.58(m, 1H), 4.60-



4.71(m, 1H), 6.80(d, J = 6.8 Hz, 1H), 7.85(d, J = 12.4 Hz, 1H), 9.05(s, 1H)


271
NMR(DMSO-d6)δ; 1.11-1.24(m, 1H), 1.26-1.49(m, 4H), 1.61-1.68(m, 1H), 1.72-



1.89(m, 10H), 1.93-2.00(m, 2H), 2.15-2.29(m, 4H), 2.45(t, J = 7.4 Hz, 2H), 3.48-3.59(m, 1H),



5.06-5.14(m, 1H), 6.05(dd, J = 2.2, 8.3 Hz, 1H), 6.75(d, J = 7.4 Hz, 1H), 7.69(d, J = 12.3 Hz, 1H),



9.03(s, 1H), 9.06(s, 1H), 12.05(brs, 1H)


297
NMR(DMSO-d6)δ; 0.27-0.32(m, 2H), 0.47-0.54(m, 2H), 1.10-1.20(m, 1H), 1.68-



1.80(m, 2H), 1.81-1.99(m, 4H), 2.13-2.25(m, 2H), 3.18(t, J = 6.2 Hz, 2H),



5.10(quintet, J = 7.0 Hz, 1H), 6.52-6.57(m, 1H), 6.85(d, J = 7.3 Hz, 1H), 7.19(d, J = 15.6 Hz, 1H),



7.55(d, J = 15.6 Hz, 1H), 7.73(d, J = 12.3 Hz, 1H), 8.24(s, 1H), 11.85(brs, 1H)


321
NMR(DMSO-d6)δ; 1.11-1.47(m, 5H), 1.49(d, J = 6.6 Hz, 6H), 1.60-1.69(m, 1H), 1.71-



1.79(m, 2H), 1.91-1.99(m, 2H), 3.52-3.63(m, 1H), 5.02(quintet, J = 6.6 Hz, 1H),



6.11(dd, J = 2.4, 8.4 Hz, 1H), 6.81(d, J = 7.3 Hz, 1H), 7.18(d, J = 15.4 Hz, 1H), 7.55(d, J = 15.6 Hz, 1H),



7.73(d, J = 12.4 Hz, 1H), 8.34(s, 1H), 11.84(s, 1H)


324
NMR(DMSO-d6)δ; 1.09-1.23(m, 1H), 1.25-1.52(m, 4H), 1.45(d, J = 6.5 Hz, 6H), 1.59-



1.68(m, 1H), 1.70-1.79(m, 2H), 1.89-2.00(m, 2H), 3.51-3.62(m, 1H),



5.01(quintet, J = 6.5 Hz, 1H), 6.15(dd, J = 2.1, 8.3 Hz, 1H), 6.80(d, J = 7.1 Hz, 1H), 7.45(s, 2H),



7.62(t, J = 7.5 Hz, 1H), 7.67-7.75(m, 2H), 7.95(d, J = 7.2 Hz, 1H), 8.30(s, 1H), 12.04(brs, 1H)


354
NMR(DMSO-d6)δ; 0.75(t, J = 7.1 Hz, 6H), 1.11-1.51(m, 5H), 1.60-2.00(m, 9H), 3.56-



3.66(m, 1H), 4.68-4.78(m, 1H), 6.08(d, J = 7.4 Hz, 1H), 6.87(d, J = 6.8 Hz, 1H),



7.22(d, J = 15.6 Hz, 1H), 7.56(d, J = 15.6 Hz, 1H), 7.73(d, J = 12.7 Hz, 1H), 8.28(s, 1H),



11.85(brs, 1H)


378
NMR(DMSO-d6)δ; 1.11-1.24(m, 1H), 1.25-1.47(m, 4H), 1.60-1.68(m, 1H), 1.71-



1.91(m, 8H), 1.92-2.00(m, 2H), 2.08-220(m, 2H), 2.46(t, J =7.2 Hz, 2H), 2.62(t, J =7.2 Hz, 2H),



3.44-3.56(m, 1H), 4.99(quintet, J = 6.6 Hz, 1H), 5.93(dd, J = 2.1, 8.2 Hz, 1H), 6.71(d, J = 7.3 Hz, 1H),



7.64(d, J = 12.5 Hz, 1H), 7.71(s, 1H), 12.11(s, 1H)


380
NMR(DMSO-d6)δ; 1.11-1.24(m, 1H), 1.27-1.48(m, 4H), 1.61-1.69(m, 1H), 1.69-



1.80(m, 4H), 1.81-1.91(m, 2H), 1.92-2.02(m, 4H), 2.13-2.23(m, 2H), 3.49-3.62(m, 1H),



5.07(quintet, J = 7.1 Hz, 1H), 6.15(dd, J = 2.3, 8.2 Hz, 1H), 6.80(d, J = 7.2 Hz, 1H),



7.18(d, J = 15.6 Hz, 1H), 7.55(d, J = 15.6 Hz, 1H), 7.72(d, J = 12.3 Hz, 1H), 8.22(s, 1H),



11.85(brs, 1H)
















TABLE 76









embedded image















No
Rb














1
—CH(Et)CO2H



2
—CH(nPr)CO2H



3
—CH(iPr)CO2H







4


embedded image









5


embedded image









6


embedded image









7
—CH2C(O)NH2



8
—CH2CH(OH)CH2CO2H



9
—(CH2)2—CH(OH)CO2H



10
—CH2CH(Me)CH2CO2H



11
—(CH2)2—CH(Me)CO2H



12
—(CH2)2—C(Me)2CO2H



13
—CH(CO2H)—(CH2)2—CO2Et



14
—CH(CO2Et)—(CH2)2—CO2H



15
—CH2C(O)NH—S(O)2Me



16
—CH2C(O)NH—S(O)2Ph







17


embedded image









18


embedded image









19
—CH(Me)—(CH2)2—CO2H



20
—(CH2)3—PO3H2







21


embedded image



















TABLE 77









embedded image















No
Rb







22
—CH(Et)CO2H



23
—CH(nPr)CO2H



24
—CH(iPr)CO2H







25


embedded image









26


embedded image









27


embedded image









28
—CH2C(O)NH2



29
—CH(Me)C(O)NH2



30
—CH2CH(OH)CH2CO2H



31
—(CH2)2—CH(OH)CO2H



32
—CH2CH(Me)CH2CO2H



33
—(CH2)2—CH(Me)CO2H



34
—(CH2)2—C(Me)2CO2H



35
—CH(CO2H)—(CH2)2—CO2Et



36
—CH(CO2Et)—(CH2)2—CO2H



37
—CH2C(O)NH—S(O)2Me



38
—CH(Me)C(O)NH—S(O)2Me



39
—CH2C(O)NH—S(O)2Ph



40
—CH(Me)C(O)NH—S(O)2Ph







41


embedded image









42


embedded image









43
—CH(Me)CO2H



44
—CH(Bn)CO2H



45
—(CH2)3—CO2H




















TABLE 78









46
—CH(CO2H)—(CH2)2—CO2H



47
—CH(Me)—(CH2)2—CO2H



48
—(CH2)3—PO3H2







49


embedded image



















TABLE 79









embedded image















No
Rb







50
—CH(nPr)CO2H







51


embedded image









52


embedded image









53


embedded image









54
—CH2C(O)NH2



55
—CH(Me)C(O)NH2



56
—CH2CH(OH)CH2CO2H



57
—(CH2)2—CH(OH)CO2H



58
—(CH2)2—C(Me)2CO2H



59
—CH(CO2H)—(CH2)2—CO2Et



60
—CH(CO2Et)—(CH2)2—CO2H



61
—CH2C(O)NH—S(O)2Me



62
—CH(Me)C(O)NH—S(O)2Me



63
—CH2C(O)NH—S(O)2Ph



64
—CH(Me)C(O)NH—S(O)2Ph







65


embedded image



















TABLE 80









embedded image















No
R5







66


embedded image









67
—(CH2)3—CO2H



68
—CH2OCH2CO2H







69


embedded image









70
—NHC(O)CH2CH(Me)CO2H



71
—NHC(O)—(CH2)2—CH(Me)CO2H



72
—NHC(O)—(CH2)2—C(Me)2CO2H







73


embedded image









74


embedded image









75


embedded image









76


embedded image









77
—(CH2)2—CO2H



78
—NHC(O)—(CH2)2—PO3H2



79
—NHC(O)CH(Me)CO2H

















TABLE 81









embedded image















No
R5







80


embedded image









81
—(CH2)3—CO2H



82
—CH2OCH2CO2H







83


embedded image









84
—NHC(O)CH2CH(Me)CO2H



85
—NHC(O)—(CH2)2—CH(Me)CO2H



86
—NHC(O)—(CH2)2—C(Me)2CO2H







87


embedded image









88


embedded image









89


embedded image









90


embedded image



















TABLE 82









embedded image















No
R5














91


embedded image









92
—(CH2)3—CO2H



93
—CH2OCH2CO2H



96
—NHC(O)CH2CH(Me)CO2H



97
—NHC(O)—(CH2)2—CH(Me)CO2H



98
—NHC(O)—(CH2)2—C(Me)2CO2H







99


embedded image









100


embedded image









101


embedded image









102
—NHC(O)CH(Me)CO2H

















TABLE 83









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No


embedded image


R5





103 104 105 106 107


embedded image


—OCH(CH3)CO2H —OCH(CH2Ph)CO2H embedded image
—NHC(O)—(CH2)3CO2H —NHC(O)—(CH2)2CO2H






108 109 110 111 112 113


embedded image


—OCH2CO2H —OCH(CH3)CO2H —OCH(CH2Ph)CO2H embedded image
—NHC(O)—(CH2)3CO2H —NHC(O)—(CH2)2CO2H






114 115 116 117 118 119


embedded image


—OCH2CO2H —OCH(CH3)CO2H —OCH(CH2Ph)CO2H embedded image
—NHC(O)—(CH2)3CO2H —NHC(O)—(CH2)2CO2H






120 121 122 123 124 125


embedded image


—OCH2CO2H —OCH(CH3)CO2H —OCH(CH2Ph)CO2H embedded image
—NHC(O)—(CH2)3CO2H —NHC(O)—(CH2)2CO2H






126 127 128 129 130 131


embedded image


—OCH2CO2H —OCH(CH3)CO2H —OCH(CH2Ph)CO2H embedded image
—NHC(O)—(CH2)3CO2H —NHC(O)—(CH2)2CO2H










INDUSTRIAL APPLICABILITY

Since the quinolone derivatives of the present invention or salts thereof have excellent platelet aggregation inhibitory activity or P2Y12 inhibitory activity, they are useful as a pharmaceutical, particularly a platelet aggregation inhibitor or a P2Y12 inhibitor. Accordingly, the compounds of the present invention are useful as a preventive and/or therapeutic agent for a circulatory organ system disease closely related to the thrombus formation by platelet aggregation, such as unstable angina, acute myocardial infarction and its secondary prevention, re-obstruction and re-stricture after coronary artery bypass surgery, PTCA operation or stent indwelling operation, coronary artery thrombolysis acceleration and re-obstruction prevention and the like ischemic diseases; transient cerebral ischemic attack (TIA) cerebral infarction, subarachnoid hemorrhage (vasospasm) and the like cerebrovascular accidents; chronic arterial occlusive disease and the like peripheral arterial diseases; and the like, and as an auxiliary agent at the time of cardiac surgical operation or vascular surgical operation.

Claims
  • 1. A quinolone derivative represented by a formula (I) or a pharmaceutically acceptable salt thereof
  • 2. The compound according to claim 1, wherein R3 is —H, —OH or —F.
  • 3. The compound according to claim 2, wherein A is CH.
  • 4. The compound according to claim 3, wherein R1 is cyclohexyl or cyclopropylmethyl.
  • 5. The compound according to claim 4, wherein R2 is —F.
  • 6. The compound according to claim 5, wherein R4 is a lower alkyl or cycloalkyl.
  • 7. The compound according to claim 6, wherein R5 is —N(R0)C(O)-lower alkylene-CO2R0, lower alkylene-CO2R0, lower alkenylene-CO2R0, —O-lower alkylene-CO2R0, —O-(lower alkylene which may be substituted with —CO2R0)-aryl or —O-lower alkenylene-CO2R0.
  • 8. The compound according to claim 1, which is selected from the group consisting of 4-{[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]amino}-4-oxobutanoic acid,5-{[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]amino}-5-oxopentanoic acid,(2E)-3-[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]acrylic acid,(2S)-2-{[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]oxy}-3-phenylpropanoic acid,(2E)-3-[7-(cyclohexylamino)-6-fluoro-1-isopropyl-4-oxo-1,4-dihydroquinolin-3-yl]acrylic acid,(2S)-2-{[7-(cyclohexylamino)-6-fluoro-1-isopropyl-4-oxo-1,4-dihydroquinolin-3-yl]oxy}-3-phenylpropanoic acid,(2S)-2-{[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]oxy}propanoic acid, and(2S)-2-{([7-(cyclohexylamino)-6-fluoro-1-isopropyl-4-oxo-1,4-dihydroquinolin-3-yl]oxy}propanoic acid,
  • 9. A pharmaceutical composition which comprises the compound or a pharmaceutically acceptable salt thereof according to claim 1, and a pharmaceutically acceptable carrier.
  • 10. The compound according to claim 1, wherein A is CH.
  • 11. The compound according to claim 1, wherein R1 is cyclohexyl or cyclopropylmethyl.
  • 12. The compound according to claim 11, wherein R2 is —F.
  • 13. The compound according to claim 12, wherein R4 is a lower alkyl or cycloalkyl.
  • 14. The compound according to claim 13, wherein R5 is —N(R0)C(O)-lower alkylene-CO2R0, lower alkylene-CO2R0, lower alkenylene-CO2R0, —O-lower alkylene-CO2R0, —O-(lower alkylene which may be substituted with —CO2R0)-aryl or —O-lower alkenylene-CO2R0.
  • 15. A compound of the formula:
  • 16. The compound according to claim 15, which is in a purified form.
  • 17. A pharmaceutical composition comprising the compound or a pharmaceutically acceptable salt thereof according to claim 15, and a pharmaceutically acceptable carrier.
  • 18. A pharmaceutical composition comprising the compound or a pharmaceutically acceptable salt thereof according to claim 16, and a pharmaceutically acceptable carrier.
Priority Claims (1)
Number Date Country Kind
2006-073045 Mar 2006 JP national
PCT Information
Filing Document Filing Date Country Kind 371c Date
PCT/JP2007/055040 3/14/2007 WO 00 9/15/2008
Publishing Document Publishing Date Country Kind
WO2007/105751 9/20/2007 WO A
US Referenced Citations (1)
Number Name Date Kind
7488739 Watanuki et al. Feb 2009 B2
Foreign Referenced Citations (12)
Number Date Country
0 614 664 Sep 1994 EP
0 945 435 Sep 1999 EP
1 650 192 Apr 2006 EP
9823592 Jun 1998 WO
0034283 Jun 2000 WO
02098856 Dec 2002 WO
03022214 Mar 2003 WO
2005000281 Jan 2005 WO
2005009971 Feb 2005 WO
WO 2005009971 Feb 2005 WO
2005035520 Apr 2005 WO
2006077851 Jul 2006 WO
Related Publications (1)
Number Date Country
20090197834 A1 Aug 2009 US