US20010000179A1 - Disubstituted pyrazolines and triazolines as factor Xa inhibitors - Google Patents

Disubstituted pyrazolines and triazolines as factor Xa inhibitors Download PDF

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US20010000179A1
US20010000179A1 US09/728,695 US72869500A US2001000179A1 US 20010000179 A1 US20010000179 A1 US 20010000179A1 US 72869500 A US72869500 A US 72869500A US 2001000179 A1 US2001000179 A1 US 2001000179A1
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phenyl
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imidazolyl
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Donald Pinto
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Bristol Myers Squibb Pharma Co
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Pinto Donald J.
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/06—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00—Drugs for disorders of the blood or the extracellular fluid
    • A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
    • C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
    • C07D249/10—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings

Definitions

  • This invention relates generally to disubstituted pyrazolines and triazolines which are inhibitors of trypsin-like serine protease enzymes, especially factor Xa, pharmaceutical compositions containing the same, and methods of using the same as anticoagulant agents for treatment and prevention of thromboembolic disorders.
  • WO 95/18111 addresses fibrinogen receptor antagonists, containing basic and acidic termini, of the formula:
  • R 1 represents the basic termini
  • U is an alkylene or heteroatom linker
  • V may be a heterocycle
  • the right hand portion of the molecule represents the acidic termini.
  • the presently claimed compounds do not contain the acidic termini of WO 95/18111.
  • heterocycle may be aromatic and groups A—B—C— and F—E—D— are attached to the ring system.
  • A—B—C— can be a wide variety of substituents including a basic group attached to an aromatic ring.
  • the F—E—D— group would appear to be an acidic functionality which differs from the present invention. Furthermore, use of these compounds as inhibitors of factor Xa is not discussed.
  • W contains an amidino, guanidino, or imino group attached to a variety of moieties including phenyl and piperidinyl
  • Y is a O, N, S, or C linker or is absent
  • X is a heterocycle
  • Z is a two atom linker containing at least one heteroatom
  • R 1 is a variety of groups including cycloalkyl, aryl, heteroaryl, and araalkyl all of which are optionally substituted.
  • a variety of proteases are described as possible targets for these compounds including Factor Xa. The presently claimed compounds differ in that they do not contain the combination R 1 —Z or Y—W.
  • WO 97/23212 describes isoxazolines, isothiazolines, and pyrazolines of the formula:
  • X is O, S or NR 15 .
  • pyrazolines of WO 97/23212 are indicated to be factor Xa inhibitors, they are not considered part of the present invention.
  • Activated factor Xa whose major practical role is the generation of thrombin by the limited proteolysis of prothrombin, holds a central position that links the intrinsic and extrinsic activation mechanisms in the final common pathway of blood coagulation.
  • the generation of thrombin, the final serine protease in the pathway to generate a fibrin clot, from its precursor is amplified by formation of prothrombinase complex (factor Xa, factor V, Ca 2+ and phospholipid).
  • factor Xa Since it is calculated that one molecule of factor Xa can generate 138 molecules of thrombin (Elodi, S., Varadi, K.: Optimization of conditions for the catalytic effect of the factor IXa-factor VIII Complex: Probable role of the complex in the amplification of blood coagulation. Thromb. Res. 1979, 15, 617-629), inhibition of factor Xa may be more efficient than inactivation of thrombin in interrupting the blood coagulation system.
  • factor Xa factor Xa
  • one object of the present invention is to provide novel disubstituted pyrazolines and triazolines which are useful as factor Xa inhibitors or pharmaceutically acceptable salts or prodrugs thereof.
  • compositions comprising a pharmaceutically acceptable carrier and a therapeutically effective amount of at least one of the compounds of the present invention or a pharmaceutically acceptable salt or prodrug form thereof.
  • It is another object of the present invention to provide a method for treating thromboembolic disorders comprising administering to a host in need of such treatment a therapeutically effective amount of at least one of the compounds of the present invention or a pharmaceutically acceptable salt or prodrug form thereof.
  • M 1 is N or CR 1c ;
  • M 2 is NR 1a or CR 1a R 1a , provided that only one of M 1 and M 2 is a N atom;
  • D is selected from C( ⁇ NR 8 )NR 7 R 9 , NHC( ⁇ NR 8 )NR 7 R 9 , NR 8 CH( ⁇ NR 7 ), C(O)NR 7 R 8 , and CR 8 R 9 NR 7 R 8 ;
  • E is selected from phenyl, pyridyl, pyrimidyl, pyrazinyl, pyridazinyl, and piperidinyl substituted with 1 R;
  • D—E—G together represent pyridyl substituted with 1 R;
  • R is selected from H, Cl, F, Br, I, (CH 2 ) t OR 3 , C 1-4 alkyl, OCF 3 , CF 3 , C(O)NR 7 R 8 , and (CR 8 R 9 ) t NR 7 R 8 ;
  • G is selected from NHCH 2 , OCH 2 , and SCH 2 , provided that when s is 0, then G is absent;
  • Z is selected from a C 1-4 alkylene, (CH 2 ) r O(CH 2 ) r , (CH 2 ) r NR 3 (CH 2 ) r , (CH 2 ) r C(O)(CH 2 ) r , (CH 2 ) r C(O)O(CH 2 ) r , (CH 2 ) r OC(O)(CH 2 ) r , (CH 2 ) r C(O)NR 3 (CH 2 ) r , (CH 2 ) r NR 3 C(O)(CH 2 ) r , (CH 2 ) r OC(O)O(CH 2 ) r , (CH 2 ) r OC(O)NR 3 (CH 2 ) r , (CH 2 ) r NR 3 C(O)O(CH 2 ) r , (CH 2 ) r NR 3 C(O)O(CH 2 ) r , (CH 2 )
  • R 1a and R 1b are, at each occurrence, independently selected from H, —(CH 2 ) r —R 1 ′, NCH 2 R 1 ′′, OCH 2 R 1 ′′, SCH 2 R 1 ′′, N(CH 2 ) 2 (CH 2 ) t R 1 ′, O(CH 2 ) 2 (CH 2 ) t R 1 ′, and S(CH 2 ) 2 (CH 2 ) t R 1 ′;
  • R 1c is selected from H, —(CH 2 ) q —R 1 ′, C 1-3 alkyl, C(O)R 2c , (CF 2 ) r CO 2 R 2c , C(O)NR 2 R 2a , C 3-6 carbocyclic residue substituted with 0-2 R 4 , and 5-10 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-2 R 4 ;
  • R 1 ′ is selected from H, C 1-3 alkyl, halo, (CF 2 ) r CF 3 , OR 2 , NR 2 R 2a , C(O)R 2c , OC(O)R 2 , (CF 2 ) r CO 2 R 2c , S(O) p R 2b , NR 2 (CH 2 ) r OR 2 , NR 2 C(O)R 2b , NR 2 C(O)NHR 2b , NR 2 C(O) 2 R 2a , OC(O)NR 2b , C(O)NR 2 R 2a , SO 2 NR 2 R 2a , NR 2 SO 2 R 2b , C 3-6 carbocyclic residue substituted with 0-2 R 4 , and 5-10 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-2 R 4 ;
  • R 1 ′′ is selected from H, C(O)R 2b , C(O)NR 2 R 2a , S(O)R 2b , S(O) 2 R 2b , and SO 2 NR 2 R 2a ;
  • R 2 is selected from H, CF 3 , C 1-6 alkyl, benzyl, C 3-6 carbocyclic residue substituted with 0-2 R 4b , and 5-6 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-2 R 4b ;
  • R 2a is selected from H, CF 3 , C 1-6 alkyl, benzyl, C 3-6 carbocyclic residue substituted with 0-2 R 4b , and 5-6 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-2 R 4b ;
  • R 2b is selected from CF 3 , C 1-4 alkoxy, C 1-6 alkyl, benzyl, C 3-6 carbocyclic residue substituted with 0-2 R 4b , and 5-6 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-2 R 4b ;
  • R 2c is selected from CF 3 , OH, C 1-4 alkoxy, C 1-6 alkyl, benzyl, C 3-6 carbocyclic residue substituted with 0-2 R 4b , and 5-6 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-2 R 4b ;
  • R 2 and R 2a combine to form a 5 or 6 membered saturated, partially saturated or unsaturated ring substituted with 0-2 R 4b which contains from 0-1 additional heteroatoms selected from the group consisting of N, O, and S;
  • R 3 at each occurrence, is selected from H, C 1-4 alkyl, and phenyl;
  • R 3a at each occurrence, is selected from H, C 1-4 alkyl, and phenyl;
  • A is selected from:
  • B is selected from:
  • X is selected from C 1-4 alkylene, —CR 2 (CR 2 R 2b )(CH 2 ) t , —C(O)—, —C( ⁇ NR)—, —CR 2 (NR 1 ′′R 2 )—, —CR 2 (OR 2 )—, —CR 2 (SR 2 )—, —C(O)CR 2 R 2a —, —CR 2 R 2a C(O), —S(O) p —, —S(O) p CR 2 R 2a —, —CR 2 R 2a S(O) p —, —S(O) 2 NR 2 —, —NR 2 S(O) 2 —, —NR 2 S(O) 2 —, —NR 2 S(O) 2 CR 2 R 2a —, —CR 2 R 2a S(O) 2 NR 2 —, —NR 2 S(O) 2 —, —NR 2 S(O) 2 CR 2a
  • Y is selected from:
  • R 4 is selected from ⁇ O, (CH 2 ) r OR 2 , halo, C 1-4 alkyl, —CN, NO 2 , (CH 2 ) r NR 2 R 2a , (CH 2 ) r C(O)R 2b , NR 2 C(O)R 2b , C(O)NR 2 R 2a , NR 2 C(O)NR 2 R 2a , CH( ⁇ NR 2 )NR 2 R 2a , NHC ( ⁇ NR 2 )NR 2 R 2a , SO 2 NR 2 R 2a , NR 2 SO 2 NR 2 R 2a , NR 2 SO 2 -C 1-4 alkyl, NR 2 SO 2 R 5 , S(O) p R 5 , (CF 2 ) r CF 3, NCH 2 R 1 ′′, OCH 2 R 1 ′′, SCH 2 R 1 ′′, N(CH 2 ) 2 (CH 2 ) t R 1 ′, O
  • one R 4 is a 5-6 membered aromatic heterocycle containing from 1-4 heteroatoms selected from the group consisting of N, O, and S;
  • R 4a is selected from ⁇ O, (CH 2 ) r OR 2 , halo, C 1-4 alkyl, —CN, NO 2 , (CH 2 ) r NR 2 R 2a , (CH 2 ) r C(O)R 2b , NR 2 C(O)R 2b , C(O)NR 2 R 2a , NR 2 C(O)NR 2 R 2a , CH( ⁇ NR 2 )NR 2 R 2a , NH 3 C( ⁇ NR 2 )NR 2 R 2a , SO 2 NR 2 R 2a , NR 2 SO 2 NR 2 R 2a , NR 2 SO 2 -C 1-4 alkyl, NR 2 SO 2 R 5 , S(O) p R 5 , and (CF 2 ) r CF 3;
  • one R 4a is a 5-6 membered aromatic heterocycle containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-1 R 5 ;
  • R 4b is selected from ⁇ O, (CH 2 ) r OR 3 , halo, C 1-4 alkyl, —CN, NO 2 , (CH 2 ) r NR 3 R 3a , (CH 2 ) r C(O)R 3 , NR 3 C(O)R 3a , C(O)NR 3 R 3a , NR 3 C(O)NR 3 R 3a , CH( ⁇ NR 3 )NR 3 R 3a , NH 3 C( ⁇ NR 3 )NR 3 R 3a , SO 2 NR 3 R 3a , NR 3 SO 2 NR 3 R 3a , NR 3 SO 2 -C 1-4 alkyl, NR 3 SO 2 CF 3 , NR 3 SO 2 -phenyl, S(O) p CF 3 , S(O) p -C 1-4 alkyl, S(O) p -phenyl, and (CF 2 ) r CF 3 , halo, C 1-4
  • R 5 at each occurrence, is selected from CF 3 , C 1-6 alkyl, phenyl substituted with 0-2 R 6 , and benzyl substituted with 0-2 R 6 ;
  • R 6 is selected from H, OH, (CH 2 ) r OR 2 , halo, C 1-4 alkyl, CN, NO 2 , (CH 2 ) r NR 2 R 2a , (CH 2 ) r C(O)R 2b , NR 2 C(O)R 2b , NR 2 C(O)NR 2 R 2a , CH( ⁇ NH)NH 2 , NHC( ⁇ NH)NH 2 , SO 2 NR 2 R 2a , NR 2 SO 2 NR 2 R 2a , and NR 2 SO 2 C 1-4 alkyl;
  • R 7 is selected from H, OH, C 1-6 alkyl, C 1-6 alkylcarbonyl, C 1-6 alkoxy, C 1-4 alkoxycarbonyl, (CH 2 ) n -phenyl, C 6-10 aryloxy, C 6-10 aryloxycarbonyl, C 6-10 arylmethylcarbonyl, C 1-4 alkylcarbonyloxy C 1-4 alkoxycarbonyl, C 6-10 arylcarbonyloxy C 1-4 alkoxycarbonyl, C 1-6 alkylaminocarbonyl, phenylaminocarbonyl, and phenyl C 1-4 alkoxycarbonyl;
  • R 8 at each occurrence, is selected from H, C 1-6 alkyl and (CH 2 ) n -phenyl;
  • R 7 and R 8 combine to form a 5 or 6 membered saturated, ring which contains from 0-1 additional heteroatoms selected from the group consisting of N, O, and S;
  • R 9 at each occurrence, is selected from H, C 1-6 alkyl and (CH 2 ) n -phenyl;
  • n at each occurrence, is selected from 0, 1, 2, and 3;
  • 63. m, at each occurrence, is selected from 0, 1, and 2;
  • p at each occurrence, is selected from 0, 1, and 2;
  • 66. r at each occurrence, is selected from 0, 1, 2, and 3;
  • 67. s, at each occurrence, is selected from 0, 1, and 2; and,
  • 68. t at each occurrence, is selected from 0 and 1.
  • Z is selected from a CH 2 O, OCH 2 , CH 2 NH, NHCH 2 , C(O), CH 2 C(O), C(O)CH 2 , NHC(O), C(O)NH, CH 2 S(O) 2 , S(O) 2 (CH 2 ), SO 2 NH, and NHSO 2 , provided that Z does not form a N—N, N—O, NCH 2 N, or NCH 2 O bond with group A;
  • A is selected from one of the following carbocyclic and heterocyclic systems which are substituted with 0-2 R 4 ; phenyl, piperidinyl, piperazinyl, pyridyl, pyrimidyl, furanyl, morpholinyl, thiophenyl, pyrrolyl, pyrrolidinyl, oxazolyl, isoxazolyl, thiazolyl, isothiazolyl, pyrazolyl, imidazolyl, oxadiazolyl, thiadiazolyl, triazolyl, 1,2,3-oxadiazolyl, 1,2,4-oxadiazolyl, 1,2,5-oxadiazolyl, 1,3,4-oxadiazolyl, 1,2,3-thiadiazolyl, 1,2,4-thiadiazolyl, 1,2,5-thiadiazolyl, 1,3,4-thiadiazolyl, 1,2,3-triazolyl, 1,2,4-triazolyl, 1,2,
  • B is selected from: Y, X—Y, NR 2 R 2a , C( ⁇ NR 2 )NR 2 R 2a , and NR 2 C( ⁇ NR 2 )NR 2 R 2a ;
  • X is selected from C 1-4 alkylene, —C(O)—, —C( ⁇ NR)—, —CR 2 (NR 2 R 2a )—, —C(O)CR 2 R 2a —, —CR 2 R 2a C(O), —C(O)NR 2 —, —NR 2 C(O)—, —C(O)NR 2 CR 2 R 2a —, —NR 2 C(O)CR 2 R 2a —, —CR 2 R 2a C(O)NR 2 —, —CR 2 R 2a NR 2 C(O)—, —NR 2 C(O)NR 2 —, —NR 2 —, —NR 2 CR 2 R 2a —, —CR 2 R 2a NR 2 —, O, —CR 2 R 2a O—, and —OCR 2 R 2a —;
  • Y is NR 2 R 2a , provided that X—Y do not form a N—N or O—N bond;
  • Y is selected from one of the following carbocyclic and heterocyclic systems which are substituted with 0-2 R 4a ;
  • Y is selected from the following bicyclic heteroaryl ring systems:
  • K is selected from O, S, NH, and N.
  • the present invention provides novel compounds of formulae Ia-Ib, wherein;
  • Z is selected from a C(O), CH 2 C(O), C(O)CH 2 , NHC(O), C(O)NH, C(O)N(CH 3 ), CH 2 S(O) 2 , S(O) 2 (CH 2 ), SO 2 NH, and NHSO 2 , provided that Z does not form a N—N or NCH 2 N bond with group A.
  • the present invention provides novel compounds of formulae Ia-Ib, wherein;
  • E is phenyl substituted with R or 2-pyridyl substituted with R;
  • D is selected from C(O)NH 2 , C( ⁇ NH)NH 2 , CH 2 NH 2 , CH 2 NHCH 3 , CH(CH 3 )NH 2 , and C(CH 3 ) 2 NH 2 ; and,
  • R is selected from H, OCH 3 , Cl, and F.
  • the present invention provides novel compounds of formulae Ia-Ib, wherein;
  • D—E is selected from 3-amidinophenyl, 3-aminomethylphenyl, 3-aminocarbonylphenyl, 3-(methylaminomethyl)phenyl, 3-(1-aminoethyl)phenyl, 3-(2-amino-2-propyl)phenyl, 4-chloro-3-amidinophenyl, 4-chloro-3-aminomethylphenyl, 4-chloro-3-(methylaminomethyl)phenyl, 4-fluoro-3-amidinophenyl, 4-fluoro-3-aminomethylphenyl, 4-fluoro-3-(methylaminomethyl)phenyl, 6-amidinopyrid-2-yl, 6-aminomethylpyrid-2-yl, 6-aminocarbonylpyrid-2-yl, 6-(methylaminomethyl)pyrid-2-yl, 6-(1-aminoethyl)pyrid-2-yl, and 6-(2-amino-2-propyl
  • the present invention provides novel compounds of formulae Ia-Ib, wherein;
  • Z is C(O)CH 2 and CONH, provided that Z does not form a N—N bond with group A;
  • A is selected from phenyl, pyridyl, and pyrimidyl, and is substituted with 0-2R 4 ; and,
  • B is selected from X—Y, phenyl, pyrrolidino, morpholino, 1,2,3-triazolyl, and imidazolyl, and is substituted with 0-1 R 4a ;
  • R 4 at each occurrence, is selected from OH, (CH 2 ) r OR 2 , halo, C 1-4 alkyl, (CH 2 ) r NR 2 R 2a , and (CF 2 ) r CF 3 ;
  • R 4a is selected from C 1-4 alkyl, CF 3 , S(O) p R 5 , SO 2 NR 2 R 2a , and 1-CF 3 -tetrazol-2-yl;
  • R 5 at each occurrence, is selected from CF 3 , C 1-6 alkyl, phenyl, and benzyl;
  • X is CH 2 or C(O);
  • Y is selected from pyrrolidino and morpholino.
  • the present invention provides novel compounds of formulae Ia-Ib, wherein;
  • A is selected from the group: phenyl, 2-pyridyl, 3-pyridyl, 2-pyrimidyl, 2-Cl-phenyl, 3-Cl-phenyl, 2-F-phenyl, 3-F-phenyl, 2-methylphenyl, 2-aminophenyl, and 2-methoxyphenyl; and,
  • B is selected from the group: 2-CF 3 -phenyl, 2-(aminosulfonyl) phenyl, 2-(methylaminosulfonyl)phenyl, 2-(dimethylaminosulfonyl)phenyl, 1-pyrrolidinocarbonyl, 2-(methylsulfonyl)phenyl, 4-morpholino, 2-(1′-CF 3 -tetrazol-2-yl)phenyl, 4-morpholinocarbonyl, 2-methyl-1-imidazolyl, 5-methyl-1-imidazolyl, 2-methylsulfonyl-1-imidazolyl and, 5-methyl-1,2,3-triazolyl.
  • the present invention provides novel compounds of formulae Ia-Ib, wherein;
  • E is phenyl substituted with R or 2-pyridyl substituted with R;
  • D is selected from C(O)NH 2 , C( ⁇ NH)NH 2 , CH 2 NH 2 , CH 2 NHCH 3 , CH(CH 3 )NH 2 , and C(CH 3 ) 2 NH 2 ; and,
  • R is selected from H, OCH 3 , Cl, and F;
  • Z is C(O)CH 2 and CONH, provided that Z does not form a N—N bond with group A;
  • A is selected from phenyl, pyridyl, and pyrimidyl, and is substituted with 0-2 R 4 ; and,
  • B is selected from X—Y, phenyl, pyrrolidino, morpholino, 1,2,3-triazolyl, and imidazolyl, and is substituted with 0-1 R 4a ;
  • R 4 at each occurrence, is selected from OH, (CH 2 ) r OR 2 , halo, C 1-4 alkyl, (CH 2 ) r NR 2 R 2a , and (CF 2 ) r CF 3 ;
  • R 4a is selected from C 1-4 alkyl, CF 3 , S(O) p R 5 , SO 2 NR 2 R 2a , and 1-CF 3 -tetrazol-2-yl;
  • R 5 at each occurrence, is selected from CF 3 , C 1-6 alkyl, phenyl, and benzyl;
  • X is CH 2 or C(O);
  • Y is selected from pyrrolidino and morpholino.
  • the present invention provides novel compounds of formulae Ia-Ib, wherein;
  • D—E is selected from 3-amidinophenyl, 3-aminomethylphenyl, 3-aminocarbonylphenyl, 3-(methylaminomethyl)phenyl, 3-(1-aminoethyl) phenyl, 3-(2-amino-2-propyl)phenyl, 4-chloro-3-amidinophenyl, 4-chloro-3-aminomethylphenyl, 4-chloro-3-(methylaminomethyl)phenyl, 4-fluoro-3-amidinophenyl, 4-fluoro-3-aminomethylphenyl, 4-fluoro-3-(methylaminomethyl) phenyl, 6-amidinopyrid-2-yl, 6-aminomethylpyrid-2-yl, 6-aminocarbonylpyrid-2-yl, 6-(methylaminomethyl)pyrid-2-yl, 6-(1-aminoethyl)pyrid-2-yl, 6-(2-amino-2-
  • A is selected from the group: phenyl, 2-pyridyl, 3-pyridyl, 2-pyrimidyl, 2-Cl-phenyl, 3-Cl-phenyl, 2-F-phenyl, 3-F-phenyl, 2-methylphenyl, 2-aminophenyl, and 2-methoxyphenyl; and,
  • B is selected from the group: 2-CF 3 -phenyl, 2-(aminosulfonyl)phenyl, 2-(methylaminosulfonyl)phenyl, 2-(dimethylaminosulfonyl)phenyl, 1-pyrrolidinocarbonyl, 2-(methylsulfonyl)phenyl, 4-morpholino, 2-(1′-CF 3 -tetrazol-2-yl)phenyl, 4-morpholinocarbonyl, 2-methyl-1-imidazolyl, 5-methyl-1-imidazolyl, 2-methylsulfonyl-1-imidazolyl and, 5-methyl-1,2,3-triazolyl.
  • the present invention provides a novel compound of formula Ia.
  • the present invention provides a novel compound of formula Ib.
  • the present invention provides novel compounds of formulae Ia-Ib, wherein;
  • D is selected from C( ⁇ NR 8 )NR 7 R 9 , C(O)NR 7 R 8 , NR 7 R 8 , and CH 2 NR 7 R 8 ;
  • E is phenyl substituted with R or pyridyl substituted with R;
  • R is selected from H, Cl, F, OR 3 , CH 3 , CH 2 CH 3 , OCF 3 , and CF 3 ;
  • Z is selected from C(O), CH 2 C(O), C(O)CH 2 , NHC(O), and C(O)NH, provided that Z does not form a N—N bond with group A;
  • R 1a and R 1b are, at each occurrence, independently selected from H, —(CH 2 ) r —R 1 ′, NCH 2 R 1 ′′, OCH 2 R 1 ′′, SCH 2 R 1 ′′, N(CH 2 )2(CH 2 ) t R 1 ′, O,(CH 2 )2(CH 2 ) t R 1 ′, and S(CH 2 )2(CH 2 ) t R 1 ;
  • R 1c is selected from H, C 1-3 alkyl, C(O)R 2c , (CF 2 ) r CO 2 R 2c , and C(O)NR 2 R 2a ;
  • R 1 ′ is selected from H, C 1-3 alkyl, halo, (CF 2 ) r CF 3 , OR 2 , NR 2 R 2a , C(O)R 2c , (CF 2 ) r CO 2 R 2c , S(O) p R 2b , NR 2 (CH 2 ) r OR 2 , NR 2 C(O)R 2b , NR 2 C(O) 2 R 2b , C(O)NR 2 R 2a , SO 2 NR 2 R 2a , and NR 2 SO 2 R 2b ;
  • A is selected from one of the following carbocyclic and heterocyclic systems which are substituted with 0-2 R 4 ;
  • B is selected from: Y, X—Y, NR 2 R 2a , C( ⁇ NR 2 )NR 2 R 2a , and NR 2 C( ⁇ NR 2 )NR 2 R 2a ;
  • X is selected from CH 2 , —CR 2 (CR 2 R 2b )(CH 2 ) t —, —C(O)—, —C( ⁇ NR)—, —CH(NR 2 R 2a )—, —C(O)NR 2 —, —NR 2 C(O)—, —NR 2 C(O)NR 2 —, —NR 2 —, and O;
  • Y is NR 2 R 2a , provided that X—Y do not form a N—N or O—N bond;
  • Y is selected from one of the following carbocyclic and heterocyclic systems which are substituted with 0-2 R 4a ;
  • R 4 at each occurrence, is selected from ⁇ O, OH, Cl, F, C 1-4 alkyl, (CH 2 ) r NR 2 R 2a , (CH 2 ) r C(O)R 2b , NR 2 C(O)R 2b , C(O)NR 2 R 2a , CH( ⁇ NH)NH 2 , NHC( ⁇ NH)NH 2 , SO 2 NR 2 R 2a , NR 2 SO 2 -C 1-4 alkyl, NR 2 SO 2 R 5 , S(O) p R 5 , and (CF 2 ) r CF 3 ;
  • R 4a is selected from ⁇ O, OH, Cl, F, C 1-4 alkyl, (CH 2 ) r NR 2 R 2a , (CH 2 ) r C(O)R 2b , NR 2 C(O)R 2b , C(O)NR 2 R 2a , CH( ⁇ NH)NH 2 , NHC( ⁇ NH)NH 2 , SO 2 NR 2 R 2a , NR 2 SO 2 -C 1-4 alkyl, NR 2 SO 2 R 5 , S(O) p R 5 , (CF 2 ) r CF 3 , and 1-CF 3 -tetrazol-2-yl;
  • R 5 at each occurrence, is selected from CF 3 , C 1-6 alkyl, phenyl substituted with 0-2 R 6 , and benzyl substituted with 0-2 R 6 ;
  • R 6 at each occurrence, is selected from H, ⁇ O, OH, OR 2 , Cl, F, CH 3 , CN, NO 2 , (CH 2 ) r NR 2 R 2a , (CH 2 ) r C(O)R 2b , NR 2 C(O)R 2b , CH( ⁇ NH)NH 2 , NHC( ⁇ NH)NH 2 , and SO 2 NR 2 R 2a ;
  • R 7 is selected from H, OH, C 1-6 alkyl, C 1-6 alkylcarbonyl, C 1-6 alkoxy, C 1-4 alkoxycarbonyl, benzyl, C 6-10 aryloxy, C 6-10 aryloxycarbonyl, C 6-10 arylmethylcarbonyl, C 1-4 alkylcarbonyloxy C 1-4 alkoxycarbonyl, C 6-10 arylcarbonyloxy C 1-4 alkoxycarbonyl, C 1-6 alkylaminocarbonyl, phenylaminocarbonyl, and phenyl C 1-4 alkoxycarbonyl;
  • R 8 at each occurrence, is selected from H, C 1-6 alkyl and benzyl;
  • R 7 and R 8 combine to form a morpholino group
  • R 9 is selected from H, C 1-6 alkyl and benzyl.
  • the present invention provides novel compounds of formulae Ia-Ib, wherein;
  • E is phenyl substituted with R or 2-pyridyl substituted with R ;
  • R is selected from H, Cl, F, OCH 3 , CH 3 , OCF 3 , and CF 3 ;
  • Z is selected from a C(O)CH 2 and C(O)NH, provided that Z does not form a N—N bond with group A;
  • R 1a is selected from H, CH 3 , CH 2 CH 3 , Cl, F, CF 3 , OCH 3 , NR 2 R 2a , S(O) p R 2b , CH 2 S(O) p R 2b , CH 2 NR 2 S(O) p R 2b , C(O)R 2c , CH 2 C(O)R 2c , C(O)NR 2 R 2a , and SO 2 NR 2 R 2a ;
  • R 1b is selected from H, CH 3 , CH 2 CH 3 , Cl, F, CF 3 , OCH 3 , NR 2 R 2a , S(O) p R 2b , CH 2 S(O) p R 2b , CH 2 NR 2 S(O) p R 2b , C(O)R 2c , CH 2 C(O)R 2c , C(O)NR 2 R 2a , and SO 2 NR 2 R 2a ;
  • R 1c is selected from H, CH 3 , CH 2 CH 3 , CF 3 , CH 2 S(O) p R 2b , CH 2 NR 2 S(O) p R 2b , C(O)R 2c , CH 2 C(O)R 2c , and C(O)NR 2 R 2a ;
  • A is selected from one of the following carbocyclic and heterocyclic systems which are substituted with 0-2 R 4 ;
  • B is selected from: Y and X—Y;
  • X is selected from CH 2 , —CR 2 (CR 2 R 2b )—, —C(O)—, —C( ⁇ NR)—, —CH(NR 2 R 2a )—, —C(O)NR 2 —, —NR 2 C(O)—, —NR 2 C(O)NR 2 —, —NR 2 —, and O;
  • Y is NR 2 R 2a , provided that X—Y do not form a N—N or O—N bond;
  • Y is selected from one of the following carbocyclic and heterocyclic systems which are substituted with 0-2 R 4a ;
  • R 2 at each occurrence, is selected from H, CF 3 , CH 3 , benzyl, and phenyl;
  • R 2a at each occurrence, is selected from H, CF 3 , CH 3 , benzyl, and phenyl;
  • R 2b at each occurrence, is selected from CF 3 , OCH 3 , CH 3 , benzyl, and phenyl;
  • R 2c at each occurrence, is selected from CF 3 , OH, OCH 3 , CH 3 , benzyl, and phenyl;
  • R 2 and R 2a combine to form a 5 or 6 membered saturated, partially unsaturated, or unsaturated ring which contains from 0-1 additional heteroatoms selected from the group consisting of N, O, and S;
  • R 3 at each occurrence, is selected from H, CH 3 , CH 2 CH 3 , and phenyl;
  • R 3a at each occurrence, is selected from H, CH 3 , CH 2 CH 3 , and phenyl;
  • R 4 at each occurrence, is selected from OH, Cl, F, CH 3 , CH 2 CH 3 , NR 2 R 2a , CH 2 NR 2 R 2a , C(O)R 2b , NR 2 C(O)R 2b , C(O)NR 2 R 2a , and CF 3 ;
  • R 4a is selected from OH, Cl, F, CH 3 , CH 2 CH 3 , NR 2 R 2a , CH 2 NR 2 R 2a , C(O)R 2b , C(O)NR 2 R 2a , SO 2 NR 2 R 2a , S(O) p R 5 , CF 3 , and 1-CF 3 -tetrazol-2-yl;
  • R 5 at each occurrence, is selected from CF 3 , C 1-6 alkyl, phenyl substituted with 0-2 R 6 , and benzyl substituted with 1 R 6 ;
  • R 6 at each occurrence, is selected from H, OH, OCH 3 , Cl, F, CH 3 , CN, NO 2 , NR 2 R 2a , CH 2 NR 2 R 2a , and SO 2 NR 2 R 2a ;
  • R 7 is selected from H, OH, C 1-3 alkyl, C 1-3 alkylcarbonyl, C 1-3 alkoxy, C 1-4 alkoxycarbonyl, benzyl, phenoxy, phenoxycarbonyl, benzylcarbonyl, C 1-4 alkylcarbonyloxy C 1-4 alkoxycarbonyl, phenylcarbonyloxy C 1-4 alkoxycarbonyl, C 1-6 alkylaminocarbonyl, phenylaminocarbonyl, and phenyl C 1-4 alkoxycarbonyl;
  • R 8 at each occurrence, is selected from H, CH 3 , and benzyl; and,
  • R 7 and R 8 combine to form a morpholino group
  • R 9 at each occurrence, is selected from H, CH 3 , and benzyl.
  • the present invention provides novel compounds of formulae Ia-Ib, wherein;
  • R 1a is selected from H, CH 3 , CH 2 CH 3 , Cl, F, CF 3 , OCH 3 , NR 2 R 2a , S(O) p R 2b , C(O)NR 2 R 2a , CH 2 S(O) p R 2b , CH 2 NR 2 S(O) p R 2b , C(O)R 2c , CH 2 C(O)R 2c , and SO 2 NR 2 R 2a ;
  • R 1b is selected from H, CH 3 , CH 2 CH 3 , Cl, F, CF 3 , OCH 3 , NR 2 R 2a , S(O) p R 2b , C(O)NR 2 R 2a , CH 2 S(O) p R 2b , CH 2 NR 2 S(O) p R 2b , C(O)R 2b , CH 2 C(O)R 2b , and SO 2 NR 2 R 2a ;
  • R 1c is selected from H, CH 3 , CH 2 CH 3 , CF 3 , C(O)NR 2 R 2a , CH 2 S(O) p R 2b , CH 2 NR 2 S(O) p R 2b , C(O)R 2b , and CH 2 C(O)R 2b ;
  • A is selected from one of the following carbocyclic and heterocyclic systems which are substituted with 0-2 R 4 ;
  • B is selected from: Y and X—Y;
  • X is selected from —C(O)— and O;
  • Y is NR 2 R 2a , provided that X—Y do not form a O—N bond;
  • Y is selected from one of the following carbocyclic and heterocyclic systems which are substituted with 0-2 R 4a ;
  • R 2 at each occurrence, is selected from H, CF 3 , CH 3 , benzyl, and phenyl;
  • R 2a is selected from H, CF 3 , CH 3 , benzyl, and phenyl;
  • R 2b at each occurrence, is selected from CF 3 , OCH 3 , CH 3 , benzyl, and phenyl;
  • R 2c at each occurrence, is selected from CF 3 , OH, OCH 3 , CH 3 , benzyl, and phenyl;
  • R 2 and R 2a combine to form a ring system selected from pyrrolidinyl, piperazinyl and morpholino;
  • R 4 at each occurrence, is selected from Cl, F, CH 3 , NR 2 R 2a , and CF 3 ;
  • R 4a at each occurrence, is selected from Cl, F, CH 3 , SO 2 NR 2 R 2a , S(O) p R 5 , and CF 3 ; and,
  • R 5 at each occurrence, is selected from CF 3 and CH 3 .
  • Specifically preferred compounds of the present invention are selected from the group:
  • the present invention provides novel pharmaceutical compositions, comprising: a pharmaceutically acceptable carrier and a therapeutically effective amount of a compound of formula (I) or a pharmaceutically acceptable salt form thereof.
  • the present invention provides a novel method for treating or preventing a thromboembolic disorder, comprising: administering to a patient in need thereof a therapeutically effective amount of a compound of formula (I) or a pharmaceutically acceptable salt form thereof.
  • the compounds herein described may have asymmetric centers.
  • substituted means that any one or more hydrogens on the designated atom is replaced with a selection from the indicated group, provided that the designated atom's normal valency is not exceeded, and that the substitution results in a stable compound.
  • a substitent is keto (i.e., ⁇ O)
  • 2 hydrogens on the atom are replaced.
  • any variable e.g., R 6
  • its definition at each occurrence is independent of its definition at every other occurrence.
  • R 6 at each occurrence is selected independently from the definition of R 6 .
  • combinations of substituents and/or variables are permissible only if such combinations result in stable compounds.
  • C 1-6 alkyl is intended to include both branched and straight-chain saturated aliphatic hydrocarbon groups having the specified number of carbon atoms, examples of which include, but are not limited to, methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, sec-butyl, t-butyl, pentyl, and hexyl;
  • Alkenyl is intended to include hydrocarbon chains of either a straight or branched configuration and one or more unsaturated carbon-carbon bonds which may occur in any stable point along the chain, such as ethenyl, propenyl, and the like.
  • Halo or “halogen” as used herein refers to fluoro, chloro, bromo, and iodo; and “counterion” is used to represent a small, negatively charged species such as chloride, bromide, hydroxide, acetate, sulfate, and the like.
  • “carbocycle” or “carbocyclic residue” is intended to mean any stable 3- to 7-membered monocyclic or bicyclic or 7- to 13-membered bicyclic or tricyclic, any of which may be saturated, partially unsaturated, or aromatic.
  • carbocycles include, but are not limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, adamantyl, cyclooctyl, [3.3.0]bicyclooctane, [4.3.0]bicyclononane, [4.4.0]bicyclodecane (decalin), [2.2.2]bicyclooctane, fluorenyl, phenyl, naphthyl, indanyl, adamantyl, or tetrahydronaphthyl (tetralin).
  • heterocycle or “heterocyclic system” is intended to mean a stable 5- to 7-membered monocyclic or bicyclic or 7- to 10-membered bicyclic heterocyclic ring which is saturated partially unsaturated or unsaturated (aromatic), and which consists of carbon atoms and from 1 to 4 heteroatoms independently selected from the group consisting of N, O and S and including any bicyclic group in which any of the above-defined heterocyclic rings is fused to a benzene ring.
  • the nitrogen and sulfur heteroatoms may optionally be oxidized.
  • the heterocyclic ring may be attached to its pendant group at any heteroatom or carbon atom which results in a stable structure.
  • the heterocyclic rings described herein may be substituted on carbon or on a nitrogen atom if the resulting compound is stable. If specifically noted, a nitrogen in the heterocycle may optionally be quaternized. It is preferred that when the total number of S and O atoms in the heterocycle exceeds 1, then these heteroatoms are not adjacent to one another. It is preferred that the total number of S and O atoms in the heterocycle is not more than 1.
  • aromatic heterocyclic system is intended to mean a stable 5- to 7-membered monocyclic or bicyclic or 7- to 10-membered bicyclic heterocyclic aromatic ring which consists of carbon atoms and from 1 to 4 heterotams independently selected from the group consisting of N, O and S. It is preferred that the total number of S and O atoms in the aromatic heterocycle is not more than 1.
  • heterocycles include, but are not limited to, 1H-indazole, 2-pyrrolidonyl, 2H,6H-1,5,2-dithiazinyl, 2H-pyrrolyl, 3H-indolyl, 4-piperidonyl, 4aH-carbazole, 4H-quinolizinyl, 6H-1,2,5-thiadiazinyl, acridinyl, azocinyl, benzimidazolyl, benzofuranyl, benzothiofuranyl, benzothiophenyl, benzoxazolyl, benzthiazolyl, benztriazolyl, benztetrazolyl, benzisoxazolyl, benzisothiazolyl, benzimidazalonyl, carbazolyl, 4aH-carbazolyl, ⁇ -carbolinyl, chromanyl, chromenyl, cinnolinyl, decahydroquinol
  • Preferred heterocycles include, but are not limited to, pyridinyl, furanyl, thienyl, pyrrolyl, pyrazolyl, imidazolyl, indolyl, benzimidazolyl, 1H-indazolyl, oxazolidinyl, benzotriazolyl, benzisoxazolyl, oxindolyl, benzoxazolinyl, or isatinoyl. Also included are fused ring and spiro compounds containing, for example, the above heterocycles.
  • phrases “pharmaceutically acceptable” is employed herein to refer to those compounds, materials, compositions, and/or dosage forms which are, within the scope of sound medical judgment, suitable for use in contact with the tissues of human beings and animals without excessive toxicity, irritation, allergic response, or other problem or complication, commensurate with a reasonable benefit/risk ratio.
  • “pharmaceutically acceptable salts” refer to derivatives of the disclosed compounds wherein the parent compound is modified by making acid or base salts thereof.
  • examples of pharmaceutically acceptable salts include, but are not limited to, mineral or organic acid salts of basic residues such as amines; alkali or organic salts of acidic residues such as carboxylic acids; and the like.
  • the pharmaceutically acceptable salts include the conventional non-toxic salts or the quaternary ammonium salts of the parent compound formed, for example, from non-toxic inorganic or organic acids.
  • such conventional non-toxic salts include those derived from inorganic acids such as hydrochloric, hydrobromic, sulfuric, sulfamic, phosphoric, nitric and the like; and the salts prepared from organic acids such as acetic, propionic, succinic, glycolic, stearic, lactic, malic, tartaric, citric, ascorbic, pamoic, maleic, hydroxymaleic, phenylacetic, glutamic, benzoic, salicylic, sulfanilic, 2-acetoxybenzoic, fumaric, toluenesulfonic, methanesulfonic, ethane disulfonic, oxalic, isethionic, and the like.
  • inorganic acids such as hydrochloric, hydrobromic, sulfuric, sulfamic, phosphoric, nitric and the like
  • organic acids such as acetic, propionic, succinic, glycolic, stearic, lactic,
  • the pharmaceutically acceptable salts of the present invention can be synthesized from the parent compound which contains a basic or acidic moiety by conventional chemical methods. Generally, such salts can be prepared by reacting the free acid or base forms of these compounds with a stoichiometric amount of the appropriate base or acid in water or in an organic solvent, or in a mixture of the two; generally, nonaqueous media like ether, ethyl acetate, ethanol, isopropanol, or acetonitrile are preferred. Lists of suitable salts are found in Remington's Pharmaceutical Sciences, 17th ed., Mack Publishing Company, Easton, Pa., 1985, p. 1418, the disclosure of which is hereby incorporated by reference.
  • Prodrugs are intended to include any covalently bonded carriers which release the active parent drug according to formula (I) in vivo when such prodrug is administered to a mammalian subject.
  • Prodrugs of a compound of formula (I) are prepared by modifying functional groups present in the compound in such a way that the modifications are cleaved, either in routine manipulation or in vivo, to the parent compound.
  • Prodrugs include compounds of formula (I) wherein a hydroxy, amino, or sulfhydryl group is bonded to any group that, when the prodrug or compound of formula (I) is administered to a mammalian subject, cleaves to form a free hydroxyl, free amino, or free sulfhydryl group, respectively.
  • prodrugs include, but are not limited to, acetate, formate and benzoate derivatives of alcohol and amine functional groups in the compounds of formula (I), and the like.
  • Preferred prodrugs are amidine prodrugs wherein D is C( ⁇ NR 7 )NH 2 or its tautomer C( ⁇ NH)NHR 7 and R 7 is selected from OH, C 1-4 alkoxy, C 6-10 aryloxy, C 1-4 alkoxycarbonyl, C 6-10 aryloxycarbonyl, C 6-10 arylmethylcarbonyl, C 1-4 alkylcarbonyloxy C 1-4 alkoxycarbonyl, and C 6-10 arylcarbonyloxy C 1-4 alkoxycarbonyl. More preferred prodrugs are where R 7 is OH, methoxy, ethoxy, benzyloxycarbonyl, methoxycarbonyl, and methylcarbonyloxymethoxycarbonyl.
  • “Stable compound” and “stable structure” are meant to indicate a compound that is sufficiently robust to survive isolation to a useful degree of purity from a reaction mixture, and formulation into an efficacious therapeutic agent.
  • the compounds of the present invention can be prepared in a number of ways known to one skilled in the art of organic synthesis.
  • the compounds of the present invention can be synthesized using the methods described below, together with synthetic methods known in the art of synthetic organic chemistry, or by variations thereon as appreciated by those skilled in the art. Preferred methods include, but are not limited to, those described below.
  • the reactions are performed in a solvent appropriate to the reagents and materials employed and suitable for the transformations being effected. It will be understood by those skilled in the art of organic synthesis that the functionality present on the molecule should be consistent with the transformations proposed. This will sometimes require a judgment to modify the order of the synthetic steps or to select one particular process scheme over another in order to obtain a desired compound of the invention.
  • Pyrazolines of this invention can be easily prepared via [3+2] cycloaddition of bromo or chloro hydrazone with an appropriate acrylate according to the methodology described by Tewari R. S. and Parihar Tetrahedron 1983, 39, 129-136, or Krayushkin, M. M. et. al Izv. Akad. Nauk, Ser. Khim. 1994, 1, 114-117.
  • Pyrazoline 5-esters can also be prepared by the treatment of an appropriately substituted hydrazone with lead tetraacetate and an appropriate acrylate in a THF/benzene solvent system according to the procedure of Sasaki T, et. al. Bull. Chem Soc. Jpn. 1970, 43, 1254.
  • pyrazoline 5-esters Another method of obtaining pyrazoline 5-esters is the condensation of an appropriate phenyl or heteroaryl hydrazine with an approptiate 2-oxoglutaconate according to Blitzke, T. et. al. J. Prakt. Chem. 1993, 335(8), 683.
  • the pyrazoline ester can be prepared by treatment of a diazo-trifluoromethyl derivative with excess acrylate or acrolein in the presence of excess pyridine (Doyle, M. O. et. al. J. Heterocyclic Chem. 1983, 20, 943).
  • the pyrazoline carboxyesters obtained via any of the above mentioned methodologies can be converted to the amide derivatives via the acid, acid chloride coupling methodlogies or a direct Weinreb (trimethylaluminum, aniline in dichloromethane) coupling technique known to those in the art of organic synthesis.
  • a variety of anilines or amines can be coupled via these methodologies to afford the desired compounds.
  • ester can be hydrolysed and converted to an amino functionality via the Curtius rearrangement. This in turn can be derivatised to obtain an amido, sulfonamido or urea derivative.
  • Pyrazolines wherein s is other than 0 can be prepared by alkylation of an appropriate pyrazoline.
  • the electrophile can consist of simple alkyl halides to heteroaryl alkyl halides.
  • Some of the heteroaryl alkyl groups can include pyridyl, pyrimidyl, imidazolyl etc.
  • D is a nitrile
  • D can be further converted to an amidine functionality via the standard Pinner-amidine reaction sequence known to those in the art or can be converted to the benzylamine via reduction in an acidic media or can be converted to the secondary and tertiary amine via the DIBAH/MeMgCl or MeMgBr/CeCl 3 methodologies outlined below.
  • Enantiomers of the pyrazolines can be easily obtained either via lipase hydrolysis of its esters or resolution with common chiral bases known to those in the art.
  • 1,2,3-Triazolines can be synthesized via the cycloaddition methodology however in this case the dipole is an aryl azide and the dipolarophile is a variety of olefins bearing an electron withdrawing group such as an ester, amide or sulfonamide.
  • 1,2,4-Triazolines can be prepared via the methods of Sandhy J. S. et. al. Heterocycles 1985, 23(5), 1143, and Heterocycles 1985, 23(5), 1123, by the method described in the scheme below.
  • the triazoline esters can then subjected to the standard coupling procedures discussed above to afford the desired amide analogs. These can then further modified to the prepare compounds of the present invention.
  • the coupling chemistry of Table B can be carried out by a variety of methods.
  • the Grignard reagent required for Y is prepared from a halogen analog of Y in dry ether, dimethoxyethane or tetrahydrofuran at 0° C. to the reflux point of the solvent. This Grignard reagent can be reacted directly under very controlled conditions, that is low temeprature ( ⁇ 20° C. or lower) and with a large excess of acid chloride or with catalytic or stoichiometric copper bromide•dimethyl sulfide complex in dimethyl sulfide as a solvent or with a variant thereof.
  • a contains: Y is: product A—X—Y: 1 A—OH Br—Y A—O—Y 2 A—CR 2 R 2a —OH Br—Y A—CR 2 R 2a O—Y 3 A—OH Br—CR 2 R 2a —Y A—OCR 2 R 2a —Y 4 A—SH Br—Y A—S—Y 5 A—CR 2 R 2a —SH Br—Y A—CR 2 R 2a S—Y 6 A—SH Br—CR 2 R 2a —Y A—SCR 2 R 2a —Y
  • the ether and thioether linkages of Table C can be prepared by reacting the two components in a polar aprotic solvent such as acetone, dimethylformamide or dimethylsulfoxide in the presence of a base such as potassium carbonate, sodium hydride or potassium t-butoxide at temperature ranging from ambient temperature to the reflux point of the solvent used.
  • a base such as potassium carbonate, sodium hydride or potassium t-butoxide
  • the thioethers of Table C serve as a convenient starting material for the preparation of the sulfoxide and sulfone analogs of Table D.
  • a combination of wet alumina and oxone can provide a reliable reagent for the oxidation of the thioether to the sulfoxide while m-chloroperbenzoic acid oxidation will give the sulfone.
  • TABLE E Rxn Q D is to be then a transformation that may be used is: 1 —CN —C( ⁇ NH)NH2 2 —CN —CH2NH2 3 —CO2H —CH2NH2 4 —CO2H —NH2
  • Table E several methods of transforming a functional group Q into group D of Formula 1 are shown. While not all possible functional groups for Q and D are listed and the synthetic methods suggested are not comprehensive, Table E is meant to illustrate strategies and transformations available to a practitioner skilled in the art of organic synthesis for preparing compounds of Formula 1.
  • reaction 1 of Table E the transformation of a nitrile into an amidine by the Pinner methodology is shown; in reaction 2 the direct reduction of a nitrile by a hydride reducing agent to a methylene amine is illustrated.
  • reaction 3 the utility of a carboxylic acid, which may be readily derived from its ester or a nitrile if necessary, in the preparation of a methylene amine is shown.
  • This synthetic route is exceptionally flexible because of the several stable intermediates prepared en route to the final product.
  • formation of an activated analog such as the mixed anhydride, allows for the mild reduction of the acid to the methylene alcohol, this may in turn be transformed into a leaving group by sulfonylation or halogenation or protected with a suitable protecting group to be transformed later in the synthesis as the chemistry demands.
  • an efficient nitrogen nucleophile such as azide anion
  • Reaction 4 addresses the problem of appending the amine functionality directly through a bond to group E of Formula 1.
  • the carboxylic acid provides a convenient entre into this selection for group D.
  • the well-know Curtius rearrangement is illustrated here; an activated acid analog can be used to form an acyl azide which upon thermal decomposition is rearranged to the corresponding isocyanate.
  • the isocyanate intermediate may then be captured as a stable carbamate by the addition of a suitable alcohol and further heating. This carbamate can be used as a stable protecting group for the amine or cleaved directly to the desired D. Alternatively, it may be convenient to quench the isocyanate intermediate with water to give the amine directly.
  • One diastereomer of a compound of Formula I may display superior activity compared with the others. Thus, the following stereochemistries are considered to be a part of the present invention.
  • racemic material can be achieved by HPLC using a chiral column or by a resolution using a resolving agent such as camphonic chloride as in Steven D. Young, et al, Antimicrobial Agents and Chemotheraphy, 1995, 2602-2605.
  • a chiral compound of Formula I may also be directly synthesized using a chiral catalyst or a chiral ligand, e.g., Andrew S. Thompson, et al, Tet. lett. 1995, 36, 8937-8940).
  • Part C The product from part B was treated with 2′-methylsulfonyl-4-amino-[1,1′]biphenyl under Weinreb conditions (trimethylaluminum in dichloromethane) to afford pure coupled product (oil) after silica gel column chromatography (hexane:ethyl acetate 7:3).
  • Part D The product from part C was subjected to the Pinner amidine reaction sequence (HCl/MeOH followed by ammonium carbonate in methanol), purified via standard HPLC purification, lyophilization to afford (40% yield) of Example 1 as colorless crystals.
  • each entry in each table is intended to be paired with each formulae at the start of the table.
  • example 1 is intended to be paired with each of formulae a-ttt and in Table 2, example 1 is intended to be paired with each of formulae a-ss.
  • the compounds of this invention are useful as anticoagulants for the treatment or prevention of thromboembolic disorders in mammals.
  • thromboembolic disorders as used herein includes arterial or venous cardiovascular or cerebrovascular thromboembolic disorders, including, for example, unstable angina, first or recurrent myocardial infarction, ischemic sudden death, transient ischemic attack, stroke, atherosclerosis, venous thrombosis, deep vein thrombosis, thrombophlebitis, arterial embolism, coronary and cerebral arterial thrombosis, cerebral embolism, kidney embolisms, and pulmonary embolisms.
  • the anticoagulant effect of compounds of the present invention is believed to be due to inhibition of factor Xa or thrombin.
  • the effectiveness of compounds of the present invention as inhibitors of factor Xa was determined using purified human factor Xa and synthetic substrate.
  • the rate of factor Xa hydrolysis of chromogenic substrate S2222 was measured both in the absence and presence of compounds of the present invention. Hydrolysis of the substrate resulted in the release of pNA, which was monitored spectrophotometrically by measuring the increase in absorbance at 405 nM. A decrease in the rate of absorbance change at 405 nm in the presence of inhibitor is indicative of enzyme inhibition.
  • the results of this assay are expressed as inhibitory constant, K i .
  • K i Factor Xa determinations were made in 0.10 M sodium phosphate buffer, pH 7.5, containing 0.20 M NaCl, and 0.5% PEG 8000.
  • the Michaelis constant, K m for substrate hydrolysis was determined at 25° C. using the method of Lineweaver and Burk. Values of K i were determined by allowing 0.2-0.5 nM human factor Xa (Enzyme Research Laboratories, South Bend, Ind.) to react with the substrate (0.20 mM-1 mM) in the presence of inhibitor. Reactions were allowed to go for 30 minutes and the velocities (rate of absorbance change vs time) were measured in the time frame of 25-30 minutes. The following relationship was used to calculate K i values:
  • v o is the velocity of the control in the absence of inhibitor
  • v s is the velocity in the presence of inhibitor
  • I is the concentration of inhibitor
  • K i is the dissociation constant of the enzyme:inhibitor complex
  • S is the concentration of substrate
  • K m is the Michaelis constant
  • the antithrombotic effect of compounds of the present invention can be demonstrated in a rabbit arterio-venous (AV) shunt thrombosis model.
  • AV arterio-venous
  • rabbits weighing 2-3 kg anesthetized with a mixture of xylazine (10 mg/kg i.m.) and ketamine (50 mg/kg i.m.) are used.
  • a saline-filled AV shunt device is connected between the femoral arterial and the femoral venous cannulae.
  • the AV shunt device consists of a piece of 6-cm tygon tubing which contains a piece of silk thread. Blood will flow from the femoral artery via the AV-shunt into the femoral vein.
  • the exposure of flowing blood to a silk thread will induce the formation of a significant thrombus.
  • the shunt is disconnected and the silk thread covered with thrombus is weighed.
  • Test agents or vehicle will be given (i.v., i.p., s.c., or orally) prior to the opening of the AV shunt.
  • the percentage inhibition of thrombus formation is determined for each treatment group.
  • the ID50 values dose which produces 50% inhibition of thrombus formation) are estimated by linear regression.
  • the compounds of formula (I) may also be useful as inhibitors of serine proteases, notably human thrombin, plasma kallikrein and plasmin. Because of their inhibitory action, these compounds are indicated for use in the prevention or treatment of physiological reactions, blood coagulation and inflammation, catalyzed by the aforesaid class of enzymes. Specifically, the compounds have utility as drugs for the treatment of diseases arising from elevated thrombin activity such as myocardial infarction, and as reagents used as anticoagulants in the processing of blood to plasma for diagnostic and other commercial purposes.
  • serine proteases notably human thrombin, plasma kallikrein and plasmin. Because of their inhibitory action, these compounds are indicated for use in the prevention or treatment of physiological reactions, blood coagulation and inflammation, catalyzed by the aforesaid class of enzymes.
  • the compounds have utility as drugs for the treatment of diseases arising from elevated thrombin activity such as myocardial infarction, and as rea
  • Some compounds of the present invention were shown to be direct acting inhibitors of the serine protease thrombin by their ability to inhibit the cleavage of small molecule substrates by thrombin in a purified system.
  • In vitro inhibition constants were determined by the method described by Kettner et al. in J. Biol. Chem. 265, 18289-18297 (1990), herein incorporated by reference.
  • thrombin-mediated hydrolysis of the chromogenic substrate S2238 Helena Laboratories, Beaumont, Tx.
  • Addition of an inhibitor to the assay mixture results in decreased absorbance and is indicative of thrombin inhibition.
  • Human thrombin (Enzyme Research Laboratories, Inc., South Bend, Ind.) at a concentration of 0.2 nM in 0.10 M sodium phosphate buffer, pH 7.5, 0.20 M NaCl, and 0.5% PEG 6000, was incubated with various substrate concentrations ranging from 0.20 to 0.02 mM. After 25 to 30 minutes of incubation, thrombin activity was assayed by monitoring the rate of increase in absorbance at 405 nm which arises owing to substrate hydrolysis. Inhibition constants were derived from reciprocal plots of the reaction velocity as a function of substrate concentration using the standard method of Lineweaver and Burk. Using the methodology described above, some compounds of this invention were evaluated and found to exhibit a K i of less than 10 ⁇ m, thereby confirming the utility of the compounds of the present invention as effective thrombin inhibitors.
  • the compounds of the present invention can be administered alone or in combination with one or more additional therapeutic agents. These include other anti-coagulant or coagulation inhibitory agents, anti-platelet or platelet inhibitory agents, thrombin inhibitors, or thrombolytic or fibrinolytic agents.
  • the compounds are administered to a mammal in a therapeutically effective amount.
  • therapeutically effective amount it is meant an amount of a compound of Formula I that, when administered alone or in combination with an additional therapeutic agent to a mammal, is effective to prevent or ameliorate the thromboembolic disease condition or the progression of the disease.
  • administered in combination or “combination therapy” it is meant that the compound of Formula I and one or more additional therapeutic agents are administered concurrently to the mammal being treated.
  • each component may be administered at the same time or sequentially in any order at different points in time.
  • each component may be administered separately but sufficiently closely in time so as to provide the desired therapeutic effect.
  • Other anticoagulant agents or coagulation inhibitory agents
  • warfarin and heparin as well as other factor Xa inhibitors such as those described in the publications identified above under Background of the Invention.
  • anti-platelet agents denotes agents that inhibit platelet function such as by inhibiting the aggregation, adhesion or granular secretion of platelets.
  • agents include, but are not limited to, the various known non-steroidal anti-inflammatory drugs (NSAIDS) such as aspirin, ibuprofen, naproxen, sulindac, indomethacin, mefenamate, droxicam, diclofenac, sulfinpyrazone, and piroxicam, including pharmaceutically acceptable salts or prodrugs thereof.
  • NSAIDS non-steroidal anti-inflammatory drugs
  • aspirin acetylsalicyclic acid or ASA
  • piroxicam are preferred.
  • Suitable anti-platelet agents include ticlopidine, including pharmaceutically acceptable salts or prodrugs thereof. Ticlopidine is also a preferred compound since it is known to be gentle on the gastro-intestinal tract in use. Still other suitable platelet inhibitory agents include IIb/IIIa antagonists, thromboxane-A2-receptor antagonists and thromboxane-A2-synthetase inhibitors, as well as pharmaceutically acceptable salts or prodrugs thereof.
  • thrombin inhibitors denotes inhibitors of the serine protease thrombin.
  • various thrombin-mediated processes such as thrombin-mediated platelet activation (that is, for example, the aggregation of platelets, and/or the granular secretion of plasminogen activator inhibitor-1 and/or serotonin) and/or fibrin formation are disrupted.
  • thrombin inhibitors are known to one of skill in the art and these inhibitors are contemplated to be used in combination with the present compounds.
  • Such inhibitors include, but are not limited to, boroarginine derivatives, boropeptides, heparins, hirudin and argatroban, including pharmaceutically acceptable salts and prodrugs thereof.
  • Boroarginine derivatives and boropeptides include N-acetyl and peptide derivatives of boronic acid, such as C-terminal a-aminoboronic acid derivatives of lysine, ornithine, arginine, homoarginine and corresponding isothiouronium analogs thereof.
  • hirudin includes suitable derivatives or analogs of hirudin, referred to herein as hirulogs, such as disulfatohirudin.
  • Boropeptide thrombin inhibitors include compounds described in Kettner et al., U.S. Pat. No. 5,187,157 and European Patent Application Publication Number 293 881 A2, the disclosures of which are hereby incorporated herein by reference.
  • Other suitable boroarginine derivatives and boropeptide thrombin inhibitors include those disclosed in PCT Application Publication Number 92/07869 and European Patent Application Publication Number 471,651 A2, the disclosures of which are hereby incorporated herein by reference.
  • thrombolytics or fibrinolytic agents (or thrombolytics or fibrinolytics), as used herein, denotes agents that lyse blood clots (thrombi).
  • agents include tissue plasminogen activator, anistreplase, urokinase or streptokinase, including pharmaceutically acceptable salts or prodrugs thereof.
  • anistreplase refers to anisoylated plasminogen streptokinase activator complex, as described, for example, in European Patent Application No. 028,489, the disclosure of which is hereby incorporated herein by reference herein.
  • urokinase as used herein, is intended to denote both dual and single chain urokinase, the latter also being referred to herein as prourokinase.
  • Administration of the compounds of Formula I of the invention in combination with such additional therapeutic agent may afford an efficacy advantage over the compounds and agents alone, and may do so while permitting the use of lower doses of each.
  • a lower dosage minimizes the potential of side effects, thereby providing an increased margin of safety.
  • the compounds of the present invention are also useful as standard or reference compounds, for example as a quality standard or control, in tests or assays involving the inhibition of factor Xa.
  • Such compounds may be provided in a commercial kit, for example, for use in pharmaceutical research involving factor Xa.
  • a compound of the present invention could be used as a reference in an assay to compare its known activity to a compound with an unknown activity. This would ensure the experimenter that the assay was being performed properly and provide a basis for comparison, especially if the test compound was a derivative of the reference compound.
  • compounds according to the present invention could be used to test their effectiveness.
  • the compounds of the present invention may also be used in diagnostic assays involving factor Xa.
  • the presence of factor Xa in an unknown sample could be determined by addition of chromogenic substrate S2222 to a series of solutions containing test sample and optionally one of the compounds of the present invention. If production of pNA is observed in the solutions containing test sample, but not in the presence of a compound of the present invention, then one would conclude factor Xa was present.
  • the compounds of this invention can be administered in such oral dosage forms as tablets, capsules (each of which includes sustained release or timed release formulations), pills, powders, granules, elixirs, tinctures, suspensions, syrups, and emulsions. They may also be administered in intravenous (bolus or infusion), intraperitoneal, subcutaneous, or intramuscular form, all using dosage forms well known to those of ordinary skill in the pharmaceutical arts. They can be administered alone, but generally will be administered with a pharmaceutical carrier selected on the basis of the chosen route of administration and standard pharmaceutical practice.
  • the dosage regimen for the compounds of the present invention will, of course, vary depending upon known factors, such as the pharmacodynamic characteristics of the particular agent and its mode and route of administration; the species, age, sex, health, medical condition, and weight of the recipient; the nature and extent of the symptoms; the kind of concurrent treatment; the frequency of treatment; the route of administration, the renal and hepatic function of the patient, and the effect desired.
  • a physician or veterinarian can determine and prescribe the effective amount of the drug required to prevent, counter, or arrest the progress of the thromboembolic disorder.
  • the daily oral dosage of each active ingredient when used for the indicated effects, will range between about 0.001 to 1000 mg/kg of body weight, preferably between about 0.01 to 100 mg/kg of body weight per day, and most preferably between about 1.0 to 20 mg/kg/day. Intravenously, the most preferred doses will range from about 1 to about 10 mg/kg/minute during a constant rate infusion.
  • Compounds of this invention may be administered in a single daily dose, or the total daily dosage may be administered in divided doses of two, three, or four times daily.
  • Compounds of this invention can be administered in intranasal form via topical use of suitable intranasal vehicles, or via transdermal routes, using transdermal skin patches.
  • the dosage administration will, of course, be continuous rather than intermittent throughout the dosage regimen.
  • the compounds are typically administered in admixture with suitable pharmaceutical diluents, excipients, or carriers (collectively referred to herein as pharmaceutical carriers) suitably selected with respect to the intended form of administration, that is, oral tablets, capsules, elixirs, syrups and the like, and consistent with conventional pharmaceutical practices.
  • suitable pharmaceutical diluents, excipients, or carriers suitably selected with respect to the intended form of administration, that is, oral tablets, capsules, elixirs, syrups and the like, and consistent with conventional pharmaceutical practices.
  • the active drug component can be combined with an oral, non-toxic, pharmaceutically acceptable, inert carrier such as lactose, starch, sucrose, glucose, methyl callulose, magnesium stearate, dicalcium phosphate, calcium sulfate, mannitol, sorbitol and the like; for oral administration in liquid form, the oral drug components can be combined with any oral, non-toxic, pharmaceutically acceptable inert carrier such as ethanol, glycerol, water, and the like.
  • suitable binders, lubricants, disintegrating agents, and coloring agents can also be incorporated into the mixture.
  • Suitable binders include starch, gelatin, natural sugars such as glucose or beta-lactose, corn sweeteners, natural and synthetic gums such as acacia, tragacanth, or sodium alginate, carboxymethylcellulose, polyethylene glycol, waxes, and the like.
  • Lubricants used in these dosage forms include sodium oleate, sodium stearate, magnesium stearate, sodium benzoate, sodium acetate, sodium chloride, and the like.
  • Disintegrators include, without limitation, starch, methyl cellulose, agar, bentonite, xanthan gum, and the like.
  • the compounds of the present invention can also be administered in the form of liposome delivery systems, such as small unilamellar vesicles, large unilamellar vesicles, and multilamellar vesicles.
  • Liposomes can be formed from a variety of phospholipids, such as cholesterol, stearylamine, or phosphatidylcholines.
  • Compounds of the present invention may also be coupled with soluble polymers as targetable drug carriers.
  • soluble polymers can include polyvinylpyrrolidone, pyran copolymer, polyhydroxypropylmethacrylamide-phenol, polyhydroxyethylaspartamidephenol, or polyethyleneoxide-polylysine substituted with palmitoyl residues.
  • the compounds of the present invention may be coupled to a class of biodegradable polymers useful in achieving controlled release of a drug, for example, polylactic acid, polyglycolic acid, copolymers of polylactic and polyglycolic acid, polyepsilon caprolactone, polyhydroxy butyric acid, polyorthoesters, polyacetals, polydihydropyrans, polycyanoacylates, and crosslinked or amphipathic block copolymers of hydrogels.
  • a drug for example, polylactic acid, polyglycolic acid, copolymers of polylactic and polyglycolic acid, polyepsilon caprolactone, polyhydroxy butyric acid, polyorthoesters, polyacetals, polydihydropyrans, polycyanoacylates, and crosslinked or amphipathic block copolymers of hydrogels.
  • Dosage forms (pharmaceutical compositions) suitable for administration may contain from about 1 milligram to about 100 milligrams of active ingredient per dosage unit.
  • the active ingredient will ordinarily be present in an amount of about 0.5-95% by weight based on the total weight of the composition.
  • Gelatin capsules may contain the active ingredient and powdered carriers, such as lactose, starch, cellulose derivatives, magnesium stearate, stearic acid, and the like. Similar diluents can be used to make compressed tablets. Both tablets and capsules can be manufactured as sustained release products to provide for continuous release of medication over a period of hours. Compressed tablets can be sugar coated or film coated to mask any unpleasant taste and protect the tablet from the atmosphere, or enteric coated for selective disintegration in the gastrointestinal tract.
  • powdered carriers such as lactose, starch, cellulose derivatives, magnesium stearate, stearic acid, and the like. Similar diluents can be used to make compressed tablets. Both tablets and capsules can be manufactured as sustained release products to provide for continuous release of medication over a period of hours. Compressed tablets can be sugar coated or film coated to mask any unpleasant taste and protect the tablet from the atmosphere, or enteric coated for selective disintegration in the gastrointestinal tract.
  • Liquid dosage forms for oral administration can contain coloring and flavoring to increase patient acceptance.
  • parenteral solutions In general, water, a suitable oil, saline, aqueous dextrose (glucose), and related sugar solutions and glycols such as propylene glycol or polyethylene glycols are suitable carriers for parenteral solutions.
  • Solutions for parenteral administration preferably contain a water soluble salt of the active ingredient, suitable stabilizing agents, and if necessary, buffer substances.
  • Antioxidizing agents such as sodium bisulfite, sodium sulfite, or ascorbic acid, either alone or combined, are suitable stabilizing agents.
  • citric acid and its salts and sodium EDTA are also used.
  • parenteral solutions can contain preservatives, such as benzalkonium chloride, methyl- or propyl-paraben, and chlorobutanol.
  • Suitable pharmaceutical carriers are described in Remington's Pharmaceutical Sciences, Mack Publishing Company, a standard reference text in this field.
  • a large number of unit capsules can be prepared by filling standard two-piece hard gelatin capsules each with 100 milligrams of powdered active ingredient, 150 milligrams of lactose, 50 milligrams of cellulose, and 6 milligrams magnesium stearate.
  • a mixture of active ingredient in a digestable oil such as soybean oil, cottonseed oil or olive oil may be prepared and injected by means of a positive displacement pump into gelatin to form soft gelatin capsules containing 100 milligrams of the active ingredient. The capsules should be washed and dried.
  • Tablets may be prepared by conventional procedures so that the dosage unit is 100 milligrams of active ingredient, 0.2 milligrams of colloidal silicon dioxide, 5 milligrams of magnesium stearate, 275 milligrams of microcrystalline cellulose, 11 milligrams of starch and 98.8 milligrams of lactose. Appropriate coatings may be applied to increase palatability or delay absorption.
  • a parenteral composition suitable for administration by injection may be prepared by stirring 1.5% by weight of active ingredient in 10% by volume propylene glycol and water. The solution should be made isotonic with sodium chloride and sterilized.
  • An aqueous suspension can be prepared for oral administration so that each 5 mL contain 100 mg of finely divided active ingredient, 200 mg of sodium carboxymethyl cellulose, 5 mg of sodium benzoate, 1.0 g of sorbitol solution, U.S.P., and 0.025 mL of vanillin.
  • a daily dosage may be about 0.1 to 100 milligrams of the compound of Formula I and about 1 to 7.5 milligrams of the second anticoagulant, per kilogram of patient body weight.
  • the compounds of this invention generally may be present in an amount of about 5 to 10 milligrams per dosage unit, and the second anti-coagulant in an amount of about 1 to 5 milligrams per dosage unit.
  • a daily dosage may be about 0.01 to 25 milligrams of the compound of Formula I and about 50 to 150 milligrams of the anti-platelet agent, preferably about 0.1 to 1 milligrams of the compound of Formula I and about 1 to 3 milligrams of antiplatelet agents, per kilogram of patient body weight.
  • a daily dosage may be about 0.1 to 1 milligrams of the compound of Formula I, per kilogram of patient body weight and, in the case of the thrombolytic agents, the usual dosage of the thrombolyic agent when administered alone may be reduced by about 70-80% when administered with a compound of Formula I.
  • the amount of each component in a typical daily dosage and typical dosage form may be reduced relative to the usual dosage of the agent when administered alone, in view of the additive or synergistic effect of the therapeutic agents when administered in combination.
  • one active ingredient may be enteric coated.
  • enteric coating one of the active ingredients it is possible not only to minimize the contact between the combined active ingredients, but also, it is possible to control the release of one of these components in the gastrointestinal tract such that one of these components is not released in the stomach but rather is released in the intestines.
  • One of the active ingredients may also be coated with a material which effects a sustained-release throughout the gastrointestinal tract and also serves to minimize physical contact between the combined active ingredients.
  • the sustained-released component can be additionally enteric coated such that the release of this component occurs only in the intestine.
  • Still another approach would involve the formulation of a combination product in which the one component is coated with a sustained and/or enteric release polymer, and the other component is also coated with a polymer such as a low-viscosity grade of hydroxypropyl methylcellulose (HPMC) or other appropriate materials as known in the art, in order to further separate the active components.
  • HPMC hydroxypropyl methylcellulose
  • the polymer coating serves to form an additional barrier to interaction with the other component.

Abstract

The present application describes disubstituted pyrazolines and triazolines of formulae I and II:
Figure US20010000179A1-20010405-C00001
or pharmaceutically acceptable salt forms thereof, wherein one of M1 and M2 maybe N and D may be a variety of N-containing groups, which are useful as inhibitors of factor Xa.

Description

    FIELD OF THE INVENTION
  • 1. This invention relates generally to disubstituted pyrazolines and triazolines which are inhibitors of trypsin-like serine protease enzymes, especially factor Xa, pharmaceutical compositions containing the same, and methods of using the same as anticoagulant agents for treatment and prevention of thromboembolic disorders.
    • BACKGROUND OF THE INVENTION
  • 2. WO 95/18111 addresses fibrinogen receptor antagonists, containing basic and acidic termini, of the formula:
    Figure US20010000179A1-20010405-C00002
  • 3. wherein R1 represents the basic termini, U is an alkylene or heteroatom linker, V may be a heterocycle, and the right hand portion of the molecule represents the acidic termini. The presently claimed compounds do not contain the acidic termini of WO 95/18111.
  • 4. In U.S. Pat. No. 5,463,071, Himmelsbach et al depict cell aggregation inhibitors which are 5-membered heterocycles of the formula:
    Figure US20010000179A1-20010405-C00003
  • 5. wherein the heterocycle may be aromatic and groups A—B—C— and F—E—D— are attached to the ring system. A—B—C— can be a wide variety of substituents including a basic group attached to an aromatic ring. The F—E—D— group, however, would appear to be an acidic functionality which differs from the present invention. Furthermore, use of these compounds as inhibitors of factor Xa is not discussed.
  • 6. WO 97/47299 describes amidino and guanidino heterocyclic protease inhibitors of the formula:
  • 7.
    Figure US20010000179A1-20010405-C00004
  • 8. wherein W contains an amidino, guanidino, or imino group attached to a variety of moieties including phenyl and piperidinyl, Y is a O, N, S, or C linker or is absent, X is a heterocycle, Z is a two atom linker containing at least one heteroatom, and R1 is a variety of groups including cycloalkyl, aryl, heteroaryl, and araalkyl all of which are optionally substituted. A variety of proteases are described as possible targets for these compounds including Factor Xa. The presently claimed compounds differ in that they do not contain the combination R1—Z or Y—W.
  • 9. WO 97/23212 describes isoxazolines, isothiazolines, and pyrazolines of the formula:
    Figure US20010000179A1-20010405-C00005
  • 10. wherein X is O, S or NR15. Though the pyrazolines of WO 97/23212 are indicated to be factor Xa inhibitors, they are not considered part of the present invention.
  • 11. Activated factor Xa, whose major practical role is the generation of thrombin by the limited proteolysis of prothrombin, holds a central position that links the intrinsic and extrinsic activation mechanisms in the final common pathway of blood coagulation. The generation of thrombin, the final serine protease in the pathway to generate a fibrin clot, from its precursor is amplified by formation of prothrombinase complex (factor Xa, factor V, Ca2+ and phospholipid). Since it is calculated that one molecule of factor Xa can generate 138 molecules of thrombin (Elodi, S., Varadi, K.: Optimization of conditions for the catalytic effect of the factor IXa-factor VIII Complex: Probable role of the complex in the amplification of blood coagulation. Thromb. Res. 1979, 15, 617-629), inhibition of factor Xa may be more efficient than inactivation of thrombin in interrupting the blood coagulation system.
  • 12. Therefore, efficacious and specific inhibitors of factor Xa are needed as potentially valuable therapeutic agents for the treatment of thromboembolic disorders. It is thus desirable to discover new factor Xa inhibitors.
    • SUMMARY OF THE INVENTION
  • 13. Accordingly, one object of the present invention is to provide novel disubstituted pyrazolines and triazolines which are useful as factor Xa inhibitors or pharmaceutically acceptable salts or prodrugs thereof.
  • 14. It is another object of the present invention to provide pharmaceutical compositions comprising a pharmaceutically acceptable carrier and a therapeutically effective amount of at least one of the compounds of the present invention or a pharmaceutically acceptable salt or prodrug form thereof.
  • 15. It is another object of the present invention to provide a method for treating thromboembolic disorders comprising administering to a host in need of such treatment a therapeutically effective amount of at least one of the compounds of the present invention or a pharmaceutically acceptable salt or prodrug form thereof.
  • 16. These and other objects, which will become apparent during the following detailed description, have been achieved by the inventors' discovery that compounds of formulae I and II:
    Figure US20010000179A1-20010405-C00006
  • 17. or pharmaceutically acceptable salt or prodrug forms thereof, wherein A, B, D, E, G, M, Z, R1a, R1b, and s are defined below, are effective factor Xa inhibitors.
    • DETAILED DESCRIPTION OF PREFERRED EMBODIMENTS
  • 18. [1] Thus, in a first embodiment, the present invention provides novel compounds of formulae I or II:
    Figure US20010000179A1-20010405-C00007
  • 19. or a stereoisomer or pharmaceutically acceptable salt thereof, wherein;
  • 20. M1 is N or CR1c;
  • 21. M2 is NR1a or CR1aR1a, provided that only one of M1 and M2 is a N atom;
  • 22. D is selected from C(═NR8)NR7R9, NHC(═NR8)NR7R9, NR8CH(═NR7), C(O)NR7R8, and CR8R9NR7R8;
  • 23. E is selected from phenyl, pyridyl, pyrimidyl, pyrazinyl, pyridazinyl, and piperidinyl substituted with 1 R;
  • 24. alternatively, D—E—G together represent pyridyl substituted with 1 R;
  • 25. R is selected from H, Cl, F, Br, I, (CH2)tOR3, C1-4 alkyl, OCF3, CF3, C(O)NR7R8, and (CR8R9)tNR7R8;
  • 26. G is selected from NHCH2, OCH2, and SCH2, provided that when s is 0, then G is absent;
  • 27. Z is selected from a C1-4 alkylene, (CH2)rO(CH2)r, (CH2)rNR3(CH2)r, (CH2)rC(O)(CH2)r, (CH2)rC(O)O(CH2)r, (CH2)rOC(O)(CH2)r, (CH2)rC(O)NR3(CH2)r, (CH2)rNR3C(O)(CH2)r, (CH2)rOC(O)O(CH2)r, (CH2)rOC(O)NR3(CH2)r, (CH2)rNR3C(O)O(CH2)r, (CH2)rNR3C(O)NR3(CH2)r, (CH2)rS(O)p(CH2)r, (CH2)rSO2NR3(CH2)r, (CH2)rNR3SO2(CH2)r, and (CH2)rNR3SO2NR3(CH2)r, provided that Z does not form a N—N, N—O, N—S, NCH2N, NCH2O, or NCH2S bond with group A;
  • 28. R1a and R1b are, at each occurrence, independently selected from H, —(CH2)r—R1′, NCH2R1″, OCH2R1″, SCH2R1″, N(CH2)2(CH2)tR1′, O(CH2)2(CH2)tR1′, and S(CH2)2(CH2)tR1′;
  • 29. R1c is selected from H, —(CH2)q—R1′, C1-3 alkyl, C(O)R2c, (CF2)rCO2R2c, C(O)NR2R2a, C3-6 carbocyclic residue substituted with 0-2 R4, and 5-10 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-2 R4;
  • 30. R1′ is selected from H, C1-3 alkyl, halo, (CF2)rCF3, OR2, NR2R2a, C(O)R2c, OC(O)R2, (CF2)rCO2R2c, S(O)pR2b, NR2(CH2)rOR2, NR2C(O)R2b, NR2C(O)NHR2b, NR2C(O)2R2a, OC(O)NR2b, C(O)NR2R2a, SO2NR2R2a, NR2SO2R2b, C3-6 carbocyclic residue substituted with 0-2 R4, and 5-10 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-2 R4;
  • 31. R1″ is selected from H, C(O)R2b, C(O)NR2R2a, S(O)R2b, S(O)2R2b, and SO2NR2R2a;
  • 32. R2, at each occurrence, is selected from H, CF3, C1-6 alkyl, benzyl, C3-6 carbocyclic residue substituted with 0-2 R4b, and 5-6 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-2 R4b;
  • 33. R2a, at each occurrence, is selected from H, CF3, C1-6 alkyl, benzyl, C3-6 carbocyclic residue substituted with 0-2 R4b, and 5-6 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-2 R4b;
  • 34. R2b, at each occurrence, is selected from CF3, C1-4 alkoxy, C1-6 alkyl, benzyl, C3-6 carbocyclic residue substituted with 0-2 R4b, and 5-6 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-2 R4b;
  • 35. R2c, at each occurrence, is selected from CF3, OH, C1-4 alkoxy, C1-6 alkyl, benzyl, C3-6 carbocyclic residue substituted with 0-2 R4b, and 5-6 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-2 R4b;
  • 36. alternatively, R2 and R2a combine to form a 5 or 6 membered saturated, partially saturated or unsaturated ring substituted with 0-2 R4b which contains from 0-1 additional heteroatoms selected from the group consisting of N, O, and S;
  • 37. R3, at each occurrence, is selected from H, C1-4 alkyl, and phenyl;
  • 38. R3a, at each occurrence, is selected from H, C1-4 alkyl, and phenyl;
  • 39. A is selected from:
  • 40. C3-10 carbocyclic residue substituted with 0-2 R4, and
  • 41. 5-10 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-2 R4;
  • 42. B is selected from:
  • 43. X—Y, NR2R2a, C(═NR2)NR2R2a, NR2C(═NR2)NR2R2a,
  • 44. C3-10 carbocyclic residue substituted with 0-2 R4a, and
  • 45. 5-10 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-2 R4a;
  • 46. X is selected from C1-4 alkylene, —CR2(CR2R2b)(CH2)t, —C(O)—, —C(═NR)—, —CR2(NR1″R2)—, —CR2(OR2)—, —CR2(SR2)—, —C(O)CR2R2a—, —CR2R2aC(O), —S(O)p—, —S(O)pCR2R2a—, —CR2R2aS(O)p—, —S(O)2NR2—, —NR2S(O)2—, —NR2S(O)2CR2R2a—, —CR2R2aS(O)2NR2—, —NR2S(O)2NR2—, —C(O)NR2—, —NR2C(O)—, —C(O)NR2CR2R2a—, —NR2C(O)CR2R2a—, —CR2R2aC(O)NR2—, —CR2R2aNR2C(O)—, —NR2C(O)O—, —OC(O)NR2—, —NR2C(O)NR2—, —NR2—, —NR2CR2R2a—, —CR2R2aNR2—, O, —CR2R2aO—, and —OCR2R2a—;
  • 47. Y is selected from:
  • 48. (CH2)rNR2R2a, provided that X—Y do not form a N—N, O—N, or S—N bond,
  • 49. C3-10 carbocyclic residue substituted with 0-2 R4a, and
  • 50. 5-10 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-2 R4a;
  • 51. R4, at each occurrence, is selected from ═O, (CH2)rOR2, halo, C1-4 alkyl, —CN, NO2, (CH2)rNR2R2a, (CH2)rC(O)R2b, NR2C(O)R2b, C(O)NR2R2a, NR2C(O)NR2R2a, CH(═NR2)NR2R2a, NHC (═NR2)NR2R2a, SO2NR2R2a, NR2SO2NR2R2a, NR2SO2-C1-4 alkyl, NR2SO2R5, S(O)pR5, (CF2)rCF3, NCH2R1″, OCH2R1″, SCH2R1″, N(CH2)2(CH2)tR1′, O(CH2)2(CH2)tR1′, and S(CH2)2(CH2)tR1″,
  • 52. alternatively, one R4 is a 5-6 membered aromatic heterocycle containing from 1-4 heteroatoms selected from the group consisting of N, O, and S;
  • 53. R4a, at each occurrence, is selected from ═O, (CH2)rOR2, halo, C1-4 alkyl, —CN, NO2, (CH2)rNR2R2a, (CH2)rC(O)R2b, NR2C(O)R2b, C(O)NR2R2a, NR2C(O)NR2R2a, CH(═NR2)NR2R2a, NH3C(═NR2)NR2R2a, SO2NR2R2a, NR2SO2NR2R2a, NR2SO2-C1-4 alkyl, NR2SO2R5, S(O)pR5, and (CF2)rCF3;
  • 54. alternatively, one R4a is a 5-6 membered aromatic heterocycle containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-1 R5;
  • 55. R4b, at each occurrence, is selected from ═O, (CH2)rOR3, halo, C1-4 alkyl, —CN, NO2, (CH2)rNR3R3a, (CH2)rC(O)R3, NR3C(O)R3a, C(O)NR3R3a, NR3C(O)NR3R3a, CH(═NR3)NR3R3a, NH3C(═NR3)NR3R3a, SO2NR3R3a, NR3SO2NR3R3a, NR3SO2-C1-4 alkyl, NR3SO2CF3, NR3SO2-phenyl, S(O)pCF3, S(O)p-C1-4 alkyl, S(O)p-phenyl, and (CF2)rCF3;
  • 56. R5, at each occurrence, is selected from CF3, C1-6 alkyl, phenyl substituted with 0-2 R6, and benzyl substituted with 0-2 R6;
  • 57. R6, at each occurrence, is selected from H, OH, (CH2)rOR2, halo, C1-4 alkyl, CN, NO2, (CH2)rNR2R2a, (CH2)rC(O)R2b, NR2C(O)R2b, NR2C(O)NR2R2a, CH(═NH)NH2, NHC(═NH)NH2, SO2NR2R2a, NR2SO2NR2R2a, and NR2SO2C1-4 alkyl;
  • 58. R7, at each occurrence, is selected from H, OH, C1-6 alkyl, C1-6 alkylcarbonyl, C1-6 alkoxy, C1-4 alkoxycarbonyl, (CH2)n-phenyl, C6-10 aryloxy, C6-10 aryloxycarbonyl, C6-10 arylmethylcarbonyl, C1-4 alkylcarbonyloxy C1-4 alkoxycarbonyl, C6-10 arylcarbonyloxy C1-4 alkoxycarbonyl, C1-6 alkylaminocarbonyl, phenylaminocarbonyl, and phenyl C1-4 alkoxycarbonyl;
  • 59. R8, at each occurrence, is selected from H, C1-6 alkyl and (CH2)n-phenyl;
  • 60. alternatively, R7 and R8 combine to form a 5 or 6 membered saturated, ring which contains from 0-1 additional heteroatoms selected from the group consisting of N, O, and S;
  • 61. R9, at each occurrence, is selected from H, C1-6 alkyl and (CH2)n-phenyl;
  • 62. n, at each occurrence, is selected from 0, 1, 2, and 3;
  • 63. m, at each occurrence, is selected from 0, 1, and 2;
  • 64. p, at each occurrence, is selected from 0, 1, and 2;
  • 65. q, at each occurrence is selected from 1 and 2;
  • 66. r, at each occurrence, is selected from 0, 1, 2, and 3;
  • 67. s, at each occurrence, is selected from 0, 1, and 2; and,
  • 68. t, at each occurrence, is selected from 0 and 1.
  • 69. [2] In a preferred embodiment, the present invention provides novel compounds of formulae Ia-Ib:
    Figure US20010000179A1-20010405-C00008
  • 70. wherein;
  • 71. Z is selected from a CH2O, OCH2, CH2NH, NHCH2, C(O), CH2C(O), C(O)CH2, NHC(O), C(O)NH, CH2S(O)2, S(O)2(CH2), SO2NH, and NHSO2, provided that Z does not form a N—N, N—O, NCH2N, or NCH2O bond with group A;
  • 72. A is selected from one of the following carbocyclic and heterocyclic systems which are substituted with 0-2 R4; phenyl, piperidinyl, piperazinyl, pyridyl, pyrimidyl, furanyl, morpholinyl, thiophenyl, pyrrolyl, pyrrolidinyl, oxazolyl, isoxazolyl, thiazolyl, isothiazolyl, pyrazolyl, imidazolyl, oxadiazolyl, thiadiazolyl, triazolyl, 1,2,3-oxadiazolyl, 1,2,4-oxadiazolyl, 1,2,5-oxadiazolyl, 1,3,4-oxadiazolyl, 1,2,3-thiadiazolyl, 1,2,4-thiadiazolyl, 1,2,5-thiadiazolyl, 1,3,4-thiadiazolyl, 1,2,3-triazolyl, 1,2,4-triazolyl, 1,2,5-triazolyl, 1,3,4-triazolyl, benzofuranyl, benzothiofuranyl, indolyl, benzimidazolyl, benzoxazolyl, benzthiazolyl, indazolyl, benzisoxazolyl, benzisothiazolyl, and isoindazolyl;
  • 73. B is selected from: Y, X—Y, NR2R2a, C(═NR2)NR2R2a, and NR2C(═NR2)NR2R2a;
  • 74. X is selected from C1-4 alkylene, —C(O)—, —C(═NR)—, —CR2(NR2R2a)—, —C(O)CR2R2a—, —CR2R2aC(O), —C(O)NR2—, —NR2C(O)—, —C(O)NR2CR2R2a—, —NR2C(O)CR2R2a—, —CR2R2aC(O)NR2—, —CR2R2aNR2C(O)—, —NR2C(O)NR2—, —NR2—, —NR2CR2R2a—, —CR2R2aNR2—, O, —CR2R2aO—, and —OCR2R2a—;
  • 75. Y is NR2R2a, provided that X—Y do not form a N—N or O—N bond;
  • 76. alternatively, Y is selected from one of the following carbocyclic and heterocyclic systems which are substituted with 0-2 R4a;
  • 77. cylcopropyl, cyclopentyl, cyclohexyl, phenyl, piperidinyl, piperazinyl, pyridyl, pyrimidyl, furanyl, morpholinyl, thiophenyl, pyrrolyl, pyrrolidinyl, oxazolyl, isoxazolyl, isoxazolinyl, thiazolyl, isothiazolyl, pyrazolyl, imidazolyl, oxadiazolyl, thiadiazolyl, triazolyl, 1,2,3-oxadiazolyl, 1,2,4-oxadiazolyl, 1,2,5-oxadiazolyl, 1,3,4-oxadiazolyl, 1,2,3-thiadiazolyl, 1,2,4-thiadiazolyl, 1,2,5-thiadiazolyl, 1,3,4-thiadiazolyl, 1,2,3-triazolyl, 1,2,4-triazolyl, 1,2,5-triazolyl, 1,3,4-triazolyl, benzofuranyl, benzothiofuranyl, indolyl, benzimidazolyl, benzoxazolyl, benzthiazolyl, indazolyl, benzisoxazolyl, benzisothiazolyl, and isoindazolyl;
  • 78. alternatively, Y is selected from the following bicyclic heteroaryl ring systems:
    Figure US20010000179A1-20010405-C00009
  • 79. K is selected from O, S, NH, and N.
  • 80. [3] In a more preferred embodiment, the present invention provides novel compounds of formulae Ia-Ib, wherein;
  • 81. Z is selected from a C(O), CH2C(O), C(O)CH2, NHC(O), C(O)NH, C(O)N(CH3), CH2S(O)2, S(O)2(CH2), SO2NH, and NHSO2, provided that Z does not form a N—N or NCH2N bond with group A.
  • 82. [4] In an even more preferred embodiment, the present invention provides novel compounds of formulae Ia-Ib, wherein;
  • 83. E is phenyl substituted with R or 2-pyridyl substituted with R;
  • 84. D is selected from C(O)NH2, C(═NH)NH2, CH2NH2, CH2NHCH3, CH(CH3)NH2, and C(CH3)2NH2; and,
  • 85. R is selected from H, OCH3, Cl, and F.
  • 86. [5] In a further preferred embodiment, the present invention provides novel compounds of formulae Ia-Ib, wherein;
  • 87. D—E is selected from 3-amidinophenyl, 3-aminomethylphenyl, 3-aminocarbonylphenyl, 3-(methylaminomethyl)phenyl, 3-(1-aminoethyl)phenyl, 3-(2-amino-2-propyl)phenyl, 4-chloro-3-amidinophenyl, 4-chloro-3-aminomethylphenyl, 4-chloro-3-(methylaminomethyl)phenyl, 4-fluoro-3-amidinophenyl, 4-fluoro-3-aminomethylphenyl, 4-fluoro-3-(methylaminomethyl)phenyl, 6-amidinopyrid-2-yl, 6-aminomethylpyrid-2-yl, 6-aminocarbonylpyrid-2-yl, 6-(methylaminomethyl)pyrid-2-yl, 6-(1-aminoethyl)pyrid-2-yl, and 6-(2-amino-2-propyl)pyrid-2-yl.
  • 88. [6] In another even more preferred embodiment, the present invention provides novel compounds of formulae Ia-Ib, wherein;
  • 89. Z is C(O)CH2 and CONH, provided that Z does not form a N—N bond with group A;
  • 90. A is selected from phenyl, pyridyl, and pyrimidyl, and is substituted with 0-2R4; and,
  • 91. B is selected from X—Y, phenyl, pyrrolidino, morpholino, 1,2,3-triazolyl, and imidazolyl, and is substituted with 0-1 R4a;
  • 92. R4, at each occurrence, is selected from OH, (CH2)rOR2, halo, C1-4 alkyl, (CH2)rNR2R2a, and (CF2)rCF3;
  • 93. R4a is selected from C1-4 alkyl, CF3, S(O)pR5, SO2NR2R2a, and 1-CF3-tetrazol-2-yl;
  • 94. R5, at each occurrence, is selected from CF3, C1-6 alkyl, phenyl, and benzyl;
  • 95. X is CH2 or C(O); and,
  • 96. Y is selected from pyrrolidino and morpholino.
  • 97. [7] In another further preferred embodiment, the present invention provides novel compounds of formulae Ia-Ib, wherein;
  • 98. A is selected from the group: phenyl, 2-pyridyl, 3-pyridyl, 2-pyrimidyl, 2-Cl-phenyl, 3-Cl-phenyl, 2-F-phenyl, 3-F-phenyl, 2-methylphenyl, 2-aminophenyl, and 2-methoxyphenyl; and,
  • 99. B is selected from the group: 2-CF3-phenyl, 2-(aminosulfonyl) phenyl, 2-(methylaminosulfonyl)phenyl, 2-(dimethylaminosulfonyl)phenyl, 1-pyrrolidinocarbonyl, 2-(methylsulfonyl)phenyl, 4-morpholino, 2-(1′-CF3-tetrazol-2-yl)phenyl, 4-morpholinocarbonyl, 2-methyl-1-imidazolyl, 5-methyl-1-imidazolyl, 2-methylsulfonyl-1-imidazolyl and, 5-methyl-1,2,3-triazolyl.
  • 100. [8] In another even more preferred embodiment, the present invention provides novel compounds of formulae Ia-Ib, wherein;
  • 101. E is phenyl substituted with R or 2-pyridyl substituted with R;
  • 102. D is selected from C(O)NH2, C(═NH)NH2, CH2NH2, CH2NHCH3, CH(CH3)NH2, and C(CH3)2NH2; and,
  • 103. R is selected from H, OCH3, Cl, and F;
  • 104. Z is C(O)CH2 and CONH, provided that Z does not form a N—N bond with group A;
  • 105. A is selected from phenyl, pyridyl, and pyrimidyl, and is substituted with 0-2 R4; and,
  • 106. B is selected from X—Y, phenyl, pyrrolidino, morpholino, 1,2,3-triazolyl, and imidazolyl, and is substituted with 0-1 R4a;
  • 107. R4, at each occurrence, is selected from OH, (CH2)rOR2, halo, C1-4 alkyl, (CH2)rNR2R2a, and (CF2)rCF3;
  • 108. R4a is selected from C1-4 alkyl, CF3, S(O)pR5, SO2NR2R2a, and 1-CF3-tetrazol-2-yl;
  • 109. R5, at each occurrence, is selected from CF3, C1-6 alkyl, phenyl, and benzyl;
  • 110. X is CH2 or C(O); and,
  • 111. Y is selected from pyrrolidino and morpholino.
  • 112. [9] In another further preferred embodiment, the present invention provides novel compounds of formulae Ia-Ib, wherein;
  • 113. D—E is selected from 3-amidinophenyl, 3-aminomethylphenyl, 3-aminocarbonylphenyl, 3-(methylaminomethyl)phenyl, 3-(1-aminoethyl) phenyl, 3-(2-amino-2-propyl)phenyl, 4-chloro-3-amidinophenyl, 4-chloro-3-aminomethylphenyl, 4-chloro-3-(methylaminomethyl)phenyl, 4-fluoro-3-amidinophenyl, 4-fluoro-3-aminomethylphenyl, 4-fluoro-3-(methylaminomethyl) phenyl, 6-amidinopyrid-2-yl, 6-aminomethylpyrid-2-yl, 6-aminocarbonylpyrid-2-yl, 6-(methylaminomethyl)pyrid-2-yl, 6-(1-aminoethyl)pyrid-2-yl, 6-(2-amino-2-propyl)pyrid-2-yl;
  • 114. A is selected from the group: phenyl, 2-pyridyl, 3-pyridyl, 2-pyrimidyl, 2-Cl-phenyl, 3-Cl-phenyl, 2-F-phenyl, 3-F-phenyl, 2-methylphenyl, 2-aminophenyl, and 2-methoxyphenyl; and,
  • 115. B is selected from the group: 2-CF3-phenyl, 2-(aminosulfonyl)phenyl, 2-(methylaminosulfonyl)phenyl, 2-(dimethylaminosulfonyl)phenyl, 1-pyrrolidinocarbonyl, 2-(methylsulfonyl)phenyl, 4-morpholino, 2-(1′-CF3-tetrazol-2-yl)phenyl, 4-morpholinocarbonyl, 2-methyl-1-imidazolyl, 5-methyl-1-imidazolyl, 2-methylsulfonyl-1-imidazolyl and, 5-methyl-1,2,3-triazolyl.
  • 116. [10] In a still further preferred embodiment, the present invention provides a novel compound of formula Ia.
  • 117. [11] In another still further preferred embodiment, the present invention provides a novel compound of formula Ib.
  • 118. [12] In another even more preferred embodiment, the present invention provides novel compounds of formulae Ia-Ib, wherein;
  • 119. D is selected from C(═NR8)NR7R9, C(O)NR7R8, NR7R8, and CH2NR7R8;
  • 120. E is phenyl substituted with R or pyridyl substituted with R;
  • 121. R is selected from H, Cl, F, OR3, CH3, CH2CH3, OCF3, and CF3;
  • 122. Z is selected from C(O), CH2C(O), C(O)CH2, NHC(O), and C(O)NH, provided that Z does not form a N—N bond with group A;
  • 123. R1a and R1b are, at each occurrence, independently selected from H, —(CH2)r—R1′, NCH2R1″, OCH2R1″, SCH2R1″, N(CH2)2(CH2)tR1′, O,(CH2)2(CH2)tR1′, and S(CH2)2(CH2)tR1;
  • 124. R1c is selected from H, C1-3 alkyl, C(O)R2c, (CF2)rCO2R2c, and C(O)NR2R2a;
  • 125. R1′, at each occurrence, is selected from H, C1-3 alkyl, halo, (CF2)rCF3, OR2, NR2R2a, C(O)R2c, (CF2)rCO2R2c, S(O)pR2b, NR2(CH2)rOR2, NR2C(O)R2b, NR2C(O)2R2b, C(O)NR2R2a, SO2NR2R2a, and NR2SO2R2b;
  • 126. A is selected from one of the following carbocyclic and heterocyclic systems which are substituted with 0-2 R4;
  • 127. phenyl, piperidinyl, piperazinyl, pyridyl, pyrimidyl, furanyl, morpholinyl, thiophenyl, pyrrolyl, pyrrolidinyl, oxazolyl, isoxazolyl, thiazolyl, isothiazolyl, pyrazolyl, and imidazolyl;
  • 128. B is selected from: Y, X—Y, NR2R2a, C(═NR2)NR2R2a, and NR2C(═NR2)NR2R2a;
  • 129. X is selected from CH2, —CR2(CR2R2b)(CH2)t—, —C(O)—, —C(═NR)—, —CH(NR2R2a)—, —C(O)NR2—, —NR2C(O)—, —NR2C(O)NR2—, —NR2—, and O;
  • 130. Y is NR2R2a, provided that X—Y do not form a N—N or O—N bond;
  • 131. alternatively, Y is selected from one of the following carbocyclic and heterocyclic systems which are substituted with 0-2 R4a;
  • 132. phenyl, piperidinyl, piperazinyl, pyridyl, pyrimidyl, furanyl, morpholinyl, thiophenyl, pyrrolyl, pyrrolidinyl, oxazolyl, isoxazolyl, isoxazolinyl, thiazolyl, isothiazolyl, pyrazolyl, imidazolyl, oxadiazolyl, thiadiazolyl, triazolyl, 1,2,3-oxadiazolyl, 1,2,4-oxadiazolyl, 1,2,5-oxadiazolyl, 1,3,4-oxadiazolyl, 1,2,3-thiadiazolyl, 1,2,4-thiadiazolyl, 1,2,5-thiadiazolyl, 1,3,4-thiadiazolyl, 1,2,3-triazolyl, 1,2,4-triazolyl, 1,2,5-triazolyl, and 1,3,4-triazolyl;
  • 133. R4, at each occurrence, is selected from ═O, OH, Cl, F, C1-4 alkyl, (CH2)rNR2R2a, (CH2)rC(O)R2b, NR2C(O)R2b, C(O)NR2R2a, CH(═NH)NH2, NHC(═NH)NH2, SO2NR2R2a, NR2SO2-C1-4 alkyl, NR2SO2R5, S(O)pR5, and (CF2)rCF3;
  • 134. R4a, at each occurrence, is selected from ═O, OH, Cl, F, C1-4 alkyl, (CH2)rNR2R2a, (CH2)rC(O)R2b, NR2C(O)R2b, C(O)NR2R2a, CH(═NH)NH2, NHC(═NH)NH2, SO2NR2R2a, NR2SO2-C1-4 alkyl, NR2SO2R5, S(O)pR5, (CF2)rCF3, and 1-CF3-tetrazol-2-yl;
  • 135. R5, at each occurrence, is selected from CF3, C1-6 alkyl, phenyl substituted with 0-2 R6, and benzyl substituted with 0-2 R6;
  • 136. R6, at each occurrence, is selected from H, ═O, OH, OR2, Cl, F, CH3, CN, NO2, (CH2)rNR2R2a, (CH2)rC(O)R2b, NR2C(O)R2b, CH(═NH)NH2, NHC(═NH)NH2, and SO2NR2R2a;
  • 137. R7, at each occurrence, is selected from H, OH, C1-6 alkyl, C1-6 alkylcarbonyl, C1-6 alkoxy, C1-4 alkoxycarbonyl, benzyl, C6-10 aryloxy, C6-10 aryloxycarbonyl, C6-10 arylmethylcarbonyl, C1-4 alkylcarbonyloxy C1-4 alkoxycarbonyl, C6-10 arylcarbonyloxy C1-4 alkoxycarbonyl, C1-6 alkylaminocarbonyl, phenylaminocarbonyl, and phenyl C1-4 alkoxycarbonyl;
  • 138. R8, at each occurrence, is selected from H, C1-6 alkyl and benzyl; and
  • 139. alternatively, R7 and R8 combine to form a morpholino group; and,
  • 140. R9, at each occurrence, is selected from H, C1-6 alkyl and benzyl.
  • 141. [13] In a another further preferred embodiment, the present invention provides novel compounds of formulae Ia-Ib, wherein;
  • 142. E is phenyl substituted with R or 2-pyridyl substituted with R ;
  • 143. R is selected from H, Cl, F, OCH3, CH3, OCF3, and CF3;
  • 144. Z is selected from a C(O)CH2 and C(O)NH, provided that Z does not form a N—N bond with group A;
  • 145. R1a, at each occurrence, is selected from H, CH3, CH2CH3, Cl, F, CF3, OCH3, NR2R2a, S(O)pR2b, CH2S(O)pR2b, CH2NR2S(O)pR2b, C(O)R2c, CH2C(O)R2c, C(O)NR2R2a, and SO2NR2R2a;
  • 146. R1b is selected from H, CH3, CH2CH3, Cl, F, CF3, OCH3, NR2R2a, S(O)pR2b, CH2S(O)pR2b, CH2NR2S(O)pR2b, C(O)R2c, CH2C(O)R2c, C(O)NR2R2a, and SO2NR2R2a;
  • 147. R1c is selected from H, CH3, CH2CH3, CF3, CH2S(O)pR2b, CH2NR2S(O)pR2b, C(O)R2c, CH2C(O)R2c, and C(O)NR2R2a;
  • 148. A is selected from one of the following carbocyclic and heterocyclic systems which are substituted with 0-2 R4;
  • 149. phenyl, pyridyl, pyrimidyl, furanyl, thiophenyl, pyrrolyl, oxazolyl, isoxazolyl, thiazolyl, isothiazolyl, pyrazolyl, and imidazolyl;
  • 150. B is selected from: Y and X—Y;
  • 151. X is selected from CH2, —CR2(CR2R2b)—, —C(O)—, —C(═NR)—, —CH(NR2R2a)—, —C(O)NR2—, —NR2C(O)—, —NR2C(O)NR2—, —NR2—, and O;
  • 152. Y is NR2R2a, provided that X—Y do not form a N—N or O—N bond;
  • 153. alternatively, Y is selected from one of the following carbocyclic and heterocyclic systems which are substituted with 0-2 R4a;
  • 154. phenyl, piperidinyl, piperazinyl, pyridyl, pyrimidyl, furanyl, morpholinyl, thiophenyl, pyrrolyl, pyrrolidinyl, oxazolyl, isoxazolyl, isoxazolinyl, thiazolyl, isothiazolyl, pyrazolyl, imidazolyl, oxadiazolyl, thiadiazolyl, triazolyl, 1,2,3-oxadiazolyl, 1,2,4-oxadiazolyl, 1,2,5-oxadiazolyl, 1,3,4-oxadiazolyl, 1,2,3-thiadiazolyl, 1,2,4-thiadiazolyl, 1,2,5-thiadiazolyl, 1,3,4-thiadiazolyl, 1,2,3-triazolyl, 1,2,4-triazolyl, 1,2,5-triazolyl, and 1,3,4-triazolyl;
  • 155. R2, at each occurrence, is selected from H, CF3, CH3, benzyl, and phenyl;
  • 156. R2a, at each occurrence, is selected from H, CF3, CH3, benzyl, and phenyl;
  • 157. R2b, at each occurrence, is selected from CF3, OCH3, CH3, benzyl, and phenyl;
  • 158. R2c, at each occurrence, is selected from CF3, OH, OCH3, CH3, benzyl, and phenyl;
  • 159. alternatively, R2 and R2a combine to form a 5 or 6 membered saturated, partially unsaturated, or unsaturated ring which contains from 0-1 additional heteroatoms selected from the group consisting of N, O, and S;
  • 160. R3, at each occurrence, is selected from H, CH3, CH2CH3, and phenyl;
  • 161. R3a, at each occurrence, is selected from H, CH3, CH2CH3, and phenyl;
  • 162. R4, at each occurrence, is selected from OH, Cl, F, CH3, CH2CH3, NR2R2a, CH2NR2R2a, C(O)R2b, NR2C(O)R2b, C(O)NR2R2a, and CF3;
  • 163. R4a, at each occurrence, is selected from OH, Cl, F, CH3, CH2CH3, NR2R2a, CH2NR2R2a, C(O)R2b, C(O)NR2R2a, SO2NR2R2a, S(O)pR5, CF3, and 1-CF3-tetrazol-2-yl;
  • 164. R5, at each occurrence, is selected from CF3, C1-6 alkyl, phenyl substituted with 0-2 R6, and benzyl substituted with 1 R6;
  • 165. R6, at each occurrence, is selected from H, OH, OCH3, Cl, F, CH3, CN, NO2, NR2R2a, CH2NR2R2a, and SO2NR2R2a;
  • 166. R7, at each occurrence, is selected from H, OH, C1-3 alkyl, C1-3 alkylcarbonyl, C1-3 alkoxy, C1-4 alkoxycarbonyl, benzyl, phenoxy, phenoxycarbonyl, benzylcarbonyl, C1-4 alkylcarbonyloxy C1-4 alkoxycarbonyl, phenylcarbonyloxy C1-4 alkoxycarbonyl, C1-6 alkylaminocarbonyl, phenylaminocarbonyl, and phenyl C1-4 alkoxycarbonyl;
  • 167. R8, at each occurrence, is selected from H, CH3, and benzyl; and,
  • 168. alternatively, R7 and R8 combine to form a morpholino group;
  • 169. R9, at each occurrence, is selected from H, CH3, and benzyl.
  • 170. [14] In a another still further preferred embodiment, the present invention provides novel compounds of formulae Ia-Ib, wherein;
  • 171. R1a, at each occurrence, is selected from H, CH3, CH2CH3, Cl, F, CF3, OCH3, NR2R2a, S(O)pR2b, C(O)NR2R2a, CH2S(O)pR2b, CH2NR2S(O)pR2b, C(O)R2c, CH2C(O)R2c, and SO2NR2R2a;
  • 172. R1b is selected from H, CH3, CH2CH3, Cl, F, CF3, OCH3, NR2R2a, S(O)pR2b, C(O)NR2R2a, CH2S(O)pR2b, CH2NR2S(O)pR2b, C(O)R2b, CH2C(O)R2b, and SO2NR2R2a;
  • 173. R1c is selected from H, CH3, CH2CH3, CF3, C(O)NR2R2a, CH2S(O)pR2b, CH2NR2S(O)pR2b, C(O)R2b, and CH2C(O)R2b;
  • 174. A is selected from one of the following carbocyclic and heterocyclic systems which are substituted with 0-2 R4;
  • 175. phenyl, pyridyl, and pyrimidyl;
  • 176. B is selected from: Y and X—Y;
  • 177. X is selected from —C(O)— and O;
  • 178. Y is NR2R2a, provided that X—Y do not form a O—N bond;
  • 179. alternatively, Y is selected from one of the following carbocyclic and heterocyclic systems which are substituted with 0-2 R4a;
  • 180. phenyl, piperazinyl, pyridyl, pyrimidyl, morpholinyl, pyrrolidinyl, imidazolyl, and 1,2,3-triazolyl;
  • 181. R2, at each occurrence, is selected from H, CF3, CH3, benzyl, and phenyl;
  • 182. R2a, at each occurrence, is selected from H, CF3, CH3, benzyl, and phenyl;
  • 183. R2b, at each occurrence, is selected from CF3, OCH3, CH3, benzyl, and phenyl;
  • 184. R2c, at each occurrence, is selected from CF3, OH, OCH3, CH3, benzyl, and phenyl;
  • 185. alternatively, R2 and R2a combine to form a ring system selected from pyrrolidinyl, piperazinyl and morpholino;
  • 186. R4, at each occurrence, is selected from Cl, F, CH3, NR2R2a, and CF3;
  • 187. R4a, at each occurrence, is selected from Cl, F, CH3, SO2NR2R2a, S(O)pR5, and CF3; and,
  • 188. R5, at each occurrence, is selected from CF3 and CH3.
  • 189. [15] Specifically preferred compounds of the present invention are selected from the group:
  • 190. 1-(3-amidinophenyl)-5-[[(2′-methylsulfonyl-[1,1′]-biphen-4-yl)-aminocarbonyl]-3-trifluoromethyl-pyrazoline; and,
  • 191. 1-(3-aminomethylphenyl)-5-[[(2′-methylsulfonyl-[1,1′]-biphen-4-yl)-aminocarbonyl]-3-trifluoromethyl-pyrazoline;
  • 192. and pharmaceutically acceptable salts thereof.
  • 193. In a second embodiment, the present invention provides novel pharmaceutical compositions, comprising: a pharmaceutically acceptable carrier and a therapeutically effective amount of a compound of formula (I) or a pharmaceutically acceptable salt form thereof.
  • 194. In a third embodiment, the present invention provides a novel method for treating or preventing a thromboembolic disorder, comprising: administering to a patient in need thereof a therapeutically effective amount of a compound of formula (I) or a pharmaceutically acceptable salt form thereof.
    • DEFINITIONS
  • 195. The compounds herein described may have asymmetric centers. Compounds of the present invention containing an asymmetrically substituted atom may be isolated in optically active or racemic forms. It is well known in the art how to prepare optically active forms, such as by resolution of racemic forms or by synthesis from optically active starting materials. Many geometric isomers of olefins, C═N double bonds, and the like can also be present in the compounds described herein, and all such stable isomers are contemplated in the present invention. Cis and trans geometric isomers of the compounds of the present invention are described and may be isolated as a mixture of isomers or as separated isomeric forms. All chiral, diastereomeric, racemic forms and all geometric isomeric forms of a structure are intended, unless the specific stereochemistry or isomeric form is specifically indicated.
  • 196. The term “substituted,” as used herein, means that any one or more hydrogens on the designated atom is replaced with a selection from the indicated group, provided that the designated atom's normal valency is not exceeded, and that the substitution results in a stable compound. When a substitent is keto (i.e., ═O), then 2 hydrogens on the atom are replaced.
  • 197. When any variable (e.g., R6) occurs more than one time in any constituent or formula for a compound, its definition at each occurrence is independent of its definition at every other occurrence. Thus, for example, if a group is shown to be substituted with 0-2 R6, then said group may optionally be substituted with up to two R6 groups and R6 at each occurrence is selected independently from the definition of R6. Also, combinations of substituents and/or variables are permissible only if such combinations result in stable compounds.
  • 198. When a bond to a substituent is shown to cross a bond connecting two atoms in a ring, then such substituent may be bonded to any atom on the ring. When a substituent is listed without indicating the atom via which such substituent is bonded to the rest of the compound of a given formula, then such substituent may be bonded via any atom in such substituent. Combinations of substituents and/or variables are permissible only if such combinations result in stable compounds.
  • 199. As used herein, “C1-6 alkyl” is intended to include both branched and straight-chain saturated aliphatic hydrocarbon groups having the specified number of carbon atoms, examples of which include, but are not limited to, methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, sec-butyl, t-butyl, pentyl, and hexyl; “Alkenyl” is intended to include hydrocarbon chains of either a straight or branched configuration and one or more unsaturated carbon-carbon bonds which may occur in any stable point along the chain, such as ethenyl, propenyl, and the like.
  • 200. “Halo” or “halogen” as used herein refers to fluoro, chloro, bromo, and iodo; and “counterion” is used to represent a small, negatively charged species such as chloride, bromide, hydroxide, acetate, sulfate, and the like.
  • 201. As used herein, “carbocycle” or “carbocyclic residue” is intended to mean any stable 3- to 7-membered monocyclic or bicyclic or 7- to 13-membered bicyclic or tricyclic, any of which may be saturated, partially unsaturated, or aromatic. Examples of such carbocycles include, but are not limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, adamantyl, cyclooctyl, [3.3.0]bicyclooctane, [4.3.0]bicyclononane, [4.4.0]bicyclodecane (decalin), [2.2.2]bicyclooctane, fluorenyl, phenyl, naphthyl, indanyl, adamantyl, or tetrahydronaphthyl (tetralin).
  • 202. As used herein, the term “heterocycle” or “heterocyclic system” is intended to mean a stable 5- to 7-membered monocyclic or bicyclic or 7- to 10-membered bicyclic heterocyclic ring which is saturated partially unsaturated or unsaturated (aromatic), and which consists of carbon atoms and from 1 to 4 heteroatoms independently selected from the group consisting of N, O and S and including any bicyclic group in which any of the above-defined heterocyclic rings is fused to a benzene ring. The nitrogen and sulfur heteroatoms may optionally be oxidized. The heterocyclic ring may be attached to its pendant group at any heteroatom or carbon atom which results in a stable structure. The heterocyclic rings described herein may be substituted on carbon or on a nitrogen atom if the resulting compound is stable. If specifically noted, a nitrogen in the heterocycle may optionally be quaternized. It is preferred that when the total number of S and O atoms in the heterocycle exceeds 1, then these heteroatoms are not adjacent to one another. It is preferred that the total number of S and O atoms in the heterocycle is not more than 1. As used herein, the term “aromatic heterocyclic system” is intended to mean a stable 5- to 7-membered monocyclic or bicyclic or 7- to 10-membered bicyclic heterocyclic aromatic ring which consists of carbon atoms and from 1 to 4 heterotams independently selected from the group consisting of N, O and S. It is preferred that the total number of S and O atoms in the aromatic heterocycle is not more than 1.
  • 203. Examples of heterocycles include, but are not limited to, 1H-indazole, 2-pyrrolidonyl, 2H,6H-1,5,2-dithiazinyl, 2H-pyrrolyl, 3H-indolyl, 4-piperidonyl, 4aH-carbazole, 4H-quinolizinyl, 6H-1,2,5-thiadiazinyl, acridinyl, azocinyl, benzimidazolyl, benzofuranyl, benzothiofuranyl, benzothiophenyl, benzoxazolyl, benzthiazolyl, benztriazolyl, benztetrazolyl, benzisoxazolyl, benzisothiazolyl, benzimidazalonyl, carbazolyl, 4aH-carbazolyl, β-carbolinyl, chromanyl, chromenyl, cinnolinyl, decahydroquinolinyl, 2H,6H-1,5,2-dithiazinyl, dihydrofuro[2,3-b]tetrahydrofuran, furanyl, furazanyl, imidazolidinyl, imidazolinyl, imidazolyl, 1H-indazolyl, indolenyl, indolinyl, indolizinyl, indolyl, isobenzofuranyl, isochromanyl, isoindazolyl, isoindolinyl, isoindolyl, isoquinolinyl, isothiazolyl, isoxazolyl, morpholinyl, naphthyridinyl, octahydroisoquinolinyl, oxadiazolyl, 1,2,3-oxadiazolyl, 1,2,4-oxadiazolyl, 1,2,5-oxadiazolyl, 1,3,4-oxadiazolyl, oxazolidinyl., oxazolyl, oxazolidinylperimidinyl, phenanthridinyl, phenanthrolinyl, phenarsazinyl, phenazinyl, phenothiazinyl, phenoxathiinyl, phenoxazinyl, phthalazinyl, piperazinyl, piperidinyl, pteridinyl, piperidonyl, 4-piperidonyl, pteridinyl, purinyl, pyranyl, pyrazinyl, pyrazolidinyl, pyrazolinyl, pyrazolyl, pyridazinyl, pyridooxazole, pyridoimidazole, pyridothiazole, pyridinyl, pyridyl, pyrimidinyl, pyrrolidinyl, pyrrolinyl, pyrrolyl, quinazolinyl, quinolinyl, 4H-quinolizinyl, quinoxalinyl, quinuclidinyl, carbolinyl, tetrahydrofuranyl, tetrahydroisoquinolinyl, tetrahydroquinolinyl, 6H-1,2,5-thiadiazinyl, 1,2,3-thiadiazolyl, 1,2,4-thiadiazolyl, 1,2,5-thiadiazolyl, 1,3,4-thiadiazolyl, thianthrenyl, thiazolyl, thienyl, thienothiazolyl, thienooxazolyl, thienoimidazolyl, thiophenyl, triazinyl, 1,2,3-triazolyl, 1,2,4-triazolyl, 1,2,5-triazolyl, 1,3,4-triazolyl, xanthenyl. Preferred heterocycles include, but are not limited to, pyridinyl, furanyl, thienyl, pyrrolyl, pyrazolyl, imidazolyl, indolyl, benzimidazolyl, 1H-indazolyl, oxazolidinyl, benzotriazolyl, benzisoxazolyl, oxindolyl, benzoxazolinyl, or isatinoyl. Also included are fused ring and spiro compounds containing, for example, the above heterocycles.
  • 204. The phrase “pharmaceutically acceptable” is employed herein to refer to those compounds, materials, compositions, and/or dosage forms which are, within the scope of sound medical judgment, suitable for use in contact with the tissues of human beings and animals without excessive toxicity, irritation, allergic response, or other problem or complication, commensurate with a reasonable benefit/risk ratio.
  • 205. As used herein, “pharmaceutically acceptable salts” refer to derivatives of the disclosed compounds wherein the parent compound is modified by making acid or base salts thereof. Examples of pharmaceutically acceptable salts include, but are not limited to, mineral or organic acid salts of basic residues such as amines; alkali or organic salts of acidic residues such as carboxylic acids; and the like. The pharmaceutically acceptable salts include the conventional non-toxic salts or the quaternary ammonium salts of the parent compound formed, for example, from non-toxic inorganic or organic acids. For example, such conventional non-toxic salts include those derived from inorganic acids such as hydrochloric, hydrobromic, sulfuric, sulfamic, phosphoric, nitric and the like; and the salts prepared from organic acids such as acetic, propionic, succinic, glycolic, stearic, lactic, malic, tartaric, citric, ascorbic, pamoic, maleic, hydroxymaleic, phenylacetic, glutamic, benzoic, salicylic, sulfanilic, 2-acetoxybenzoic, fumaric, toluenesulfonic, methanesulfonic, ethane disulfonic, oxalic, isethionic, and the like.
  • 206. The pharmaceutically acceptable salts of the present invention can be synthesized from the parent compound which contains a basic or acidic moiety by conventional chemical methods. Generally, such salts can be prepared by reacting the free acid or base forms of these compounds with a stoichiometric amount of the appropriate base or acid in water or in an organic solvent, or in a mixture of the two; generally, nonaqueous media like ether, ethyl acetate, ethanol, isopropanol, or acetonitrile are preferred. Lists of suitable salts are found in Remington's Pharmaceutical Sciences, 17th ed., Mack Publishing Company, Easton, Pa., 1985, p. 1418, the disclosure of which is hereby incorporated by reference.
  • 207. “Prodrugs” are intended to include any covalently bonded carriers which release the active parent drug according to formula (I) in vivo when such prodrug is administered to a mammalian subject. Prodrugs of a compound of formula (I) are prepared by modifying functional groups present in the compound in such a way that the modifications are cleaved, either in routine manipulation or in vivo, to the parent compound. Prodrugs include compounds of formula (I) wherein a hydroxy, amino, or sulfhydryl group is bonded to any group that, when the prodrug or compound of formula (I) is administered to a mammalian subject, cleaves to form a free hydroxyl, free amino, or free sulfhydryl group, respectively. Examples of prodrugs include, but are not limited to, acetate, formate and benzoate derivatives of alcohol and amine functional groups in the compounds of formula (I), and the like. Preferred prodrugs are amidine prodrugs wherein D is C(═NR7)NH2 or its tautomer C(═NH)NHR7 and R7 is selected from OH, C1-4 alkoxy, C6-10 aryloxy, C1-4 alkoxycarbonyl, C6-10 aryloxycarbonyl, C6-10 arylmethylcarbonyl, C1-4 alkylcarbonyloxy C1-4 alkoxycarbonyl, and C6-10 arylcarbonyloxy C1-4 alkoxycarbonyl. More preferred prodrugs are where R7 is OH, methoxy, ethoxy, benzyloxycarbonyl, methoxycarbonyl, and methylcarbonyloxymethoxycarbonyl.
  • 208. “Stable compound” and “stable structure” are meant to indicate a compound that is sufficiently robust to survive isolation to a useful degree of purity from a reaction mixture, and formulation into an efficacious therapeutic agent.
    • SYNTHESIS
  • 209. The compounds of the present invention can be prepared in a number of ways known to one skilled in the art of organic synthesis. The compounds of the present invention can be synthesized using the methods described below, together with synthetic methods known in the art of synthetic organic chemistry, or by variations thereon as appreciated by those skilled in the art. Preferred methods include, but are not limited to, those described below. The reactions are performed in a solvent appropriate to the reagents and materials employed and suitable for the transformations being effected. It will be understood by those skilled in the art of organic synthesis that the functionality present on the molecule should be consistent with the transformations proposed. This will sometimes require a judgment to modify the order of the synthetic steps or to select one particular process scheme over another in order to obtain a desired compound of the invention. It will also be recognized that another major consideration in the planning of any synthetic route in this field is the judicious choice of the protecting group used for protection of the reactive functional groups present in the compounds described in this invention. An authoritative account describing the many alternatives to the trained practitioner is Greene and Wuts (Protective Groups In Organic Synthesis, Wiley and Sons, 1991). All references cited herein are hereby incorporated in their entirety herein by reference.
  • 210. Pyrazolines of this invention can be easily prepared via [3+2] cycloaddition of bromo or chloro hydrazone with an appropriate acrylate according to the methodology described by Tewari R. S. and Parihar Tetrahedron 1983, 39, 129-136, or Krayushkin, M. M. et. al Izv. Akad. Nauk, Ser. Khim. 1994, 1, 114-117.
    Figure US20010000179A1-20010405-C00010
  • 211. Pyrazoline 5-esters can also be prepared by the treatment of an appropriately substituted hydrazone with lead tetraacetate and an appropriate acrylate in a THF/benzene solvent system according to the procedure of Sasaki T, et. al. Bull. Chem Soc. Jpn. 1970, 43, 1254.
    Figure US20010000179A1-20010405-C00011
  • 212. Another method of obtaining pyrazoline 5-esters is the condensation of an appropriate phenyl or heteroaryl hydrazine with an approptiate 2-oxoglutaconate according to Blitzke, T. et. al. J. Prakt. Chem. 1993, 335(8), 683.
    Figure US20010000179A1-20010405-C00012
  • 213. Alternatively the pyrazoline ester can be prepared by treatment of a diazo-trifluoromethyl derivative with excess acrylate or acrolein in the presence of excess pyridine (Doyle, M. O. et. al. J. Heterocyclic Chem. 1983, 20, 943).
    Figure US20010000179A1-20010405-C00013
  • 214. Cycloadditions as described above but with di-substituted olefins should result in the formation of regio-adducts which can be easily separated by standard chromatographic techniques.
    Figure US20010000179A1-20010405-C00014
  • 215. It is understood by those in the art of organic synthesis that such cycloadditions can also be carried out with a wide variety of electron withdrawing olefins with functionalities such as nitro, sulfonyl, sulfonamido, nitrile, phosphate etc. These in turn can be derivatized to appropriate compounds of the present invention.
  • 216. The pyrazoline carboxyesters obtained via any of the above mentioned methodologies can be converted to the amide derivatives via the acid, acid chloride coupling methodlogies or a direct Weinreb (trimethylaluminum, aniline in dichloromethane) coupling technique known to those in the art of organic synthesis. A variety of anilines or amines can be coupled via these methodologies to afford the desired compounds.
    Figure US20010000179A1-20010405-C00015
  • 217. Alternatively the ester can be hydrolysed and converted to an amino functionality via the Curtius rearrangement. This in turn can be derivatised to obtain an amido, sulfonamido or urea derivative.
    Figure US20010000179A1-20010405-C00016
  • 218. Pyrazolines wherein s is other than 0 can be prepared by alkylation of an appropriate pyrazoline.
    Figure US20010000179A1-20010405-C00017
  • 219. The electrophile can consist of simple alkyl halides to heteroaryl alkyl halides. Some of the heteroaryl alkyl groups can include pyridyl, pyrimidyl, imidazolyl etc.
  • 220. In cases wherein D is a nitrile can be further converted to an amidine functionality via the standard Pinner-amidine reaction sequence known to those in the art or can be converted to the benzylamine via reduction in an acidic media or can be converted to the secondary and tertiary amine via the DIBAH/MeMgCl or MeMgBr/CeCl3 methodologies outlined below.
    Figure US20010000179A1-20010405-C00018
  • 221. Compounds wherein D is a nitro can be reduced under catalytic Pd/C/MeOH techniques or SnCl2/EtOAc or Zn/AcOH conditions to afford the desired amino derivatives.
  • 222. Enantiomers of the pyrazolines can be easily obtained either via lipase hydrolysis of its esters or resolution with common chiral bases known to those in the art.
  • 223. 1,2,3-Triazolines can be synthesized via the cycloaddition methodology however in this case the dipole is an aryl azide and the dipolarophile is a variety of olefins bearing an electron withdrawing group such as an ester, amide or sulfonamide.
    Figure US20010000179A1-20010405-C00019
  • 224. 1,2,4-Triazolines can be prepared via the methods of Sandhy J. S. et. al. Heterocycles 1985, 23(5), 1143, and Heterocycles 1985, 23(5), 1123, by the method described in the scheme below.
    Figure US20010000179A1-20010405-C00020
  • 225. The triazoline esters can then subjected to the standard coupling procedures discussed above to afford the desired amide analogs. These can then further modified to the prepare compounds of the present invention.
  • 226. Compounds of the present invention wherein AB is a biphenylamine or similar amine may be prepared as shown in the following scheme. 4-Bromoaniline can be protected as Boc-derivative and coupled to a phenylboronic acid under Suzuki conditions (Bioorg. Med. Chem. Lett. 1994, 189). Deprotection with TFA provides the aminobiphenyl compound. Other similar amines wherein A and/or B are heterocycles can be prepared by the same method using appropiately substituted boronic acids and arylbromide. The bromoaniline can also be linked to the core ring structures first as described above, and then undergo a Suzuki reaction to give the desired product.
    Figure US20010000179A1-20010405-C00021
  • 227. Compounds of the present invention wherein A—B is A—X—Y can be prepared like the piperazine derivative shown below.
    Figure US20010000179A1-20010405-C00022
  • 228. The following scheme shows how one can couple cyclic groups wherein X═NH, O, or S.
    Figure US20010000179A1-20010405-C00023
  • 229. When B is defined as X—Y, the following description applies. Groups A and B are available either through commercial sources, known in the literature or readily synthesized by the adaptation of standard procedures known to practioners skilled in the art of organic synthesis. The required reactive functional groups appended to analogs of A and B are also available either through commercial sources, known in the literature or readily synthesized by the adaptation of standard procedures known to practioners skilled in the art of organic synthesis. In the tables that follow the chemistry required to effect the coupling of A to B is outlined.
    TABLE A
    Preparation of Amide, Ester, Urea, Sulfonamide and
    then the reactive to give the
    substituent of following product
    Rxn. No. if A contains: Y is: A—X—Y:
    1 A—NHR2 as a ClC(O)—Y A—NR2—C(O)—Y
    substituent
    2 a secondary NH as part ClC(O)—Y A—C(O)—Y
    of a ring or chain
    3 A—OH as a ClC(O)—Y A—O—C(O)—Y
    substituent
    4 A—NHR2 as a ClC(O)—CR2R2a—Y A—NR2—C(O)—CR2R2a—Y
    substituent
    5 a secondary NH as part ClC(O)—CR2R2a—Y A—C(O)—CR2R2a—Y
    of a ring or chain
    6 A—OH as a ClC(O)—CR2R2a—Y A—O—C(O)—CR2R2a—Y
    substituent
    7 A—NHR3 as a ClC(O)NR2—Y A—NR2—C(O)NR2—Y
    substituent
    8 a secondary NH as part ClC(O)NR2—Y A—C(O)NR2—Y
    of a ring or chain
    9 A—OH as a ClC(O)NR2—Y A—O—C(O)NR2—Y
    substituent
    10 A—NHR2 as a ClSO2—Y A—NR2—SO2—Y
    substituent
    11 a secondary NH as part ClSO2—Y A—SO2—Y
    of a ring or chain
    12 A—NHR2 as a ClSO2—CR2R2a—Y A—NR2—SO2—CR2R2a—Y
    substituent
    13 a secondary NH as part ClSO2—CR2R2a—Y A—SO2—CR2R2a—Y
    of a ring or chain
    14 A—NHR2 as a ClSO2—NR2—Y A—NR2—SO2—NR2—Y
    substituent
    15 a secondary NH as part ClSO2—NR2—Y A—SO2—NR2—Y
    of a ring or chain
    16 A—C(O)Cl HO—Y as a A—C(O)—O—Y
    substituent
    17 A—C(O)Cl NHR2—Y as a A—C(O)—NR2—Y
    substituent
    18 A—C(O)Cl a secondary NH as part A—C(O)—Y
    of a ring or chain
    19 A—CR2R2aC(O)Cl HO—Y as a A—CR2R2aC(O)—O—Y
    substituent
    20 A—CR2R2aC(O)Cl NHR2—Y as a A—CR2R2aC(O)—NR2—Y
    substituent
    21 A—CR2R2aC(O)Cl a secondary NH as part A—CR2R2aC(O)—Y
    of a ring or chain
    22 A—SO2Cl NHR2—Y as a A—SO2—NR2—Y
    substituent
    23 A—SO2Cl a secondary NH as part A—SO2—Y
    of a ring or chain
    24 A—CR2R2aSO2Cl NHR2—Y as a A—CR2R2aSO2—NR2—Y
    substituent
    25 A—CR2R2aSO2Cl a secondary NH as part A—CR2R2aSO2—Y
    of a ring or chain
  • 230. The chemistry of Table A can be carried out in aprotic solvents such as a chlorocarbon, pyridine, benzene or toluene, at temperatures ranging from −20° C. to the reflux point of the solvent and with or without a trialkylamine base.
    TABLE B
    then the reactive to give the
    Rxn. substituent of following product
    No. if A contains: Y is: A—X—Y:
    1 A—C(O)Cl BrMg—Y A—C(O)—Y
    2 A—CR2R2aC(O)Cl BrMg—Y A—CR2R2a 2C(O)—Y
    3 A—C(O)Cl BrMgCR2R2a—Y A—C(O)CR2R2a—Y
    4 A—CR2R2aC(O)Cl BrMgCR2R2a—Y A—
    CR2R2aC(O)CR2R2a—Y
  • 231. The coupling chemistry of Table B can be carried out by a variety of methods. The Grignard reagent required for Y is prepared from a halogen analog of Y in dry ether, dimethoxyethane or tetrahydrofuran at 0° C. to the reflux point of the solvent. This Grignard reagent can be reacted directly under very controlled conditions, that is low temeprature (−20° C. or lower) and with a large excess of acid chloride or with catalytic or stoichiometric copper bromide•dimethyl sulfide complex in dimethyl sulfide as a solvent or with a variant thereof. Other methods available include transforming the Grignard reagent to the cadmium reagent and coupling according to the procedure of Carson and Prout (Org. Syn. Col. Vol. 3 (1955) 601) or a coupling mediated by Fe(acac)3 according to Fiandanese et al.(Tetrahedron Lett., (1984) 4805), or a coupling mediated by manganese (II) catalysis (Cahiez and Laboue, Tetrahedron Lett., 33(31), (1992) 4437).
    TABLE C
    Preparation of ether and thioether linkages
    then the reactive to give the
    Rxn. substituent of following
    No. if A contains: Y is: product A—X—Y:
    1 A—OH Br—Y A—O—Y
    2 A—CR2R2a—OH Br—Y A—CR2R2aO—Y
    3 A—OH Br—CR2R2a—Y A—OCR2R2a—Y
    4 A—SH Br—Y A—S—Y
    5 A—CR2R2a—SH Br—Y A—CR2R2aS—Y
    6 A—SH Br—CR2R2a—Y A—SCR2R2a—Y
  • 232. The ether and thioether linkages of Table C can be prepared by reacting the two components in a polar aprotic solvent such as acetone, dimethylformamide or dimethylsulfoxide in the presence of a base such as potassium carbonate, sodium hydride or potassium t-butoxide at temperature ranging from ambient temperature to the reflux point of the solvent used.
    TABLE D
    Preparation of —SO— and —SO2— linkages from
    thioethers of Table 3.
    and it is oxidized and it is oxidized
    with Alumina with m-chloroper-
    (wet)/Oxone benzoic acid
    if the (Greenhalgh, (Satoh et al.,
    Rxn. starting Synlett, (1992) Chem. Lett. (1992)
    No. material is: 235) the product is: 381), the product is:
    1 A—S—Y A—S(O)—Y A—SO2—Y
    2 A—CR2R2aS—Y A—CR2R2aS(O)—Y A—CR2R2aSO2—Y
    3 A—SCR2R2a—Y A—S(O)CR2R2a—Y A—SO2CR2R2a—Y
  • 233. The thioethers of Table C serve as a convenient starting material for the preparation of the sulfoxide and sulfone analogs of Table D. A combination of wet alumina and oxone can provide a reliable reagent for the oxidation of the thioether to the sulfoxide while m-chloroperbenzoic acid oxidation will give the sulfone.
    TABLE E
    Rxn Q D is to be then a transformation that may be used is:
    1 —CN —C(═NH)NH2
    2 —CN —CH2NH2
    3 —CO2H —CH2NH2
    4 —CO2H —NH2
  • 234. In Table E several methods of transforming a functional group Q into group D of Formula 1 are shown. While not all possible functional groups for Q and D are listed and the synthetic methods suggested are not comprehensive, Table E is meant to illustrate strategies and transformations available to a practitioner skilled in the art of organic synthesis for preparing compounds of Formula 1. In reaction 1 of Table E the transformation of a nitrile into an amidine by the Pinner methodology is shown; in reaction 2 the direct reduction of a nitrile by a hydride reducing agent to a methylene amine is illustrated. In reaction 3, the utility of a carboxylic acid, which may be readily derived from its ester or a nitrile if necessary, in the preparation of a methylene amine is shown. This synthetic route is exceptionally flexible because of the several stable intermediates prepared en route to the final product. As outlined, formation of an activated analog, such as the mixed anhydride, allows for the mild reduction of the acid to the methylene alcohol, this may in turn be transformed into a leaving group by sulfonylation or halogenation or protected with a suitable protecting group to be transformed later in the synthesis as the chemistry demands. Once the methylene alcohol is so activated, displacement by an efficient nitrogen nucleophile, such as azide anion, can again provide another suitably stable analog, —the methylene azide— which may be used as a protected form of the methylene amine or transformed directly into the methylene amine group by reduction. Reaction 4 addresses the problem of appending the amine functionality directly through a bond to group E of Formula 1. Once again, the carboxylic acid provides a convenient entre into this selection for group D. The well-know Curtius rearrangement is illustrated here; an activated acid analog can be used to form an acyl azide which upon thermal decomposition is rearranged to the corresponding isocyanate. The isocyanate intermediate may then be captured as a stable carbamate by the addition of a suitable alcohol and further heating. This carbamate can be used as a stable protecting group for the amine or cleaved directly to the desired D. Alternatively, it may be convenient to quench the isocyanate intermediate with water to give the amine directly.
  • 235. One diastereomer of a compound of Formula I may display superior activity compared with the others. Thus, the following stereochemistries are considered to be a part of the present invention.
    Figure US20010000179A1-20010405-C00024
  • 236. When required, separation of the racemic material can be achieved by HPLC using a chiral column or by a resolution using a resolving agent such as camphonic chloride as in Steven D. Young, et al, Antimicrobial Agents and Chemotheraphy, 1995, 2602-2605. A chiral compound of Formula I may also be directly synthesized using a chiral catalyst or a chiral ligand, e.g., Andrew S. Thompson, et al, Tet. lett. 1995, 36, 8937-8940).
  • 237. Other features of the invention will become apparent in the course of the following descriptions of exemplary embodiments which are given for illustration of the invention and are not intended to be limiting thereof.
    • EXAMPLES EXAMPLES 1 AND 2
  • 238. 1-(3-Amidinophenyl)-5-[[(2′-methylsulfonyl-[1,1′]-biphen-4-yl)-aminocarbonyl]-3-trifluoromethyl-pyrazoline and 1-(3-aminomethylphenyl)-5-[[(2′-methylsulfonyl-[1,1′]-biphen-4-yl)-aminocarbonyl]-3-trifluoromethyl-pyrazoline
  • 239. Part A: To a methanolic solution containing meta-cyanophenyl-hydrazine (2 g, 15.03 mmol) was added trifluoromethylacetaldehyde hydrate (1.74 g, 15.03 mmol). The reaction mixture was heated to gentle reflux overnight. Methanol was stripped off to afford yellow crystals of pure hydrazone (2.99g, 93%). 1HNMR (CDCl3)δ: 10.10 (bs, 1H), 7.33 (m, 2H), 7.10 (m, 2H) ppm; ESI (-ve) mass spectrum analysis m/z (relative intensity) 212 (M-H, 100).
  • 240. Part B: NCS (1.02 g, 7.69 mmol) was added to a DMF (25 mL) solution of the compound prepared in part A (1.64 g, 7.69 mmol). The reaction mixture was stirred at room temperature over night, quenched with water (500 mL) and organics extracted with ethyl acetate (2×100 mL) dried (MgSO4) and evaporated to a reddish brown oil. The oil was redissolved in chloroform (25 mL) and to this solution was added ethyl acrylate (10 mL) followed by slow addition of triethylamine (0.81 mL, 5.75 mmoL). The reaction mixture was refluxed for 18h cooled and quenched with dil. hydrochloric acid (1N, 20 mL). The organic layer was separated and evaporated to an oil. Chromatography on silica gel (7:3, Hexane:ethylacetate) afforded a colorless oil which solidified on standing (1.5 g, 62%). 1HNMR(CDCl3)δ: 7.40-7.22 (m, 4H), 4.89 (dd, J=6.2 and 13.4 Hz, 1H), 4.24 (q, 2H), 3.63-3.50 (dd, J=1.9 and 13.2 Hz, 1H), 3.38 (dd, J=1.9 and 14 Hz, 1H), 1.23 (t, 3H) ppm; ESI mass spectrum analysis m/z (relative intensity) 312 (M+H, 100).
  • 241. Part C: The product from part B was treated with 2′-methylsulfonyl-4-amino-[1,1′]biphenyl under Weinreb conditions (trimethylaluminum in dichloromethane) to afford pure coupled product (oil) after silica gel column chromatography (hexane:ethyl acetate 7:3). 1HNMR(CDCl3)δ: 8.40 (bs, 1H), 8.17 (dd, J=1.1 and 7.8 Hz, 1H), 7.65-7.25 (m, 11H), 4.90 (m, 1H), 3.78 (m, 1H), 3.38 (dd, J=1.5 and 8.1 Hz, 1H), 2.69 s, 3H); ESI (-ve) mass spectrum analysis m/z (rel. intensity) 511 (M-H, 100).
  • 242. Part D: The product from part C was subjected to the Pinner amidine reaction sequence (HCl/MeOH followed by ammonium carbonate in methanol), purified via standard HPLC purification, lyophilization to afford (40% yield) of Example 1 as colorless crystals. 1HNMR(DMSO6)δ: 9.36 (bs, 1.5H), 9.00 (bs, 1.5 Hz), 8.06 (d, J=7.7 Hz, 1H), 7.53-7.78 (m, 6H), 7.35 (d, J=8.1 Hz, 3H), 7.27 (d, J=8.0 Hz, 1H), 7.17 (d, J=8.5 Hz, 1H), 5.33 (dd, J=6.2 and 13.2 Hz, 1H), 3.76 (t, 1H), 3.40 (d, J=3.1 Hz, 1H), 2.84(s, 3H) ppm; ESI (+ve) mass spectum analysis m/z (relative intensity) 530 (M+H, 100).
  • 243. Additionally, the compound form Part C was subjected to reduction using 10% Pd/C in an acidic medium (methanol/acetic acid). Purification via standard HPLC techniques and lyophilization afforded the benzylamine (10% yield). 1HNMR(DMSO6)δ: 8.07 (bs, 2H), 8.01 (d, J=8 Hz, 1H), 7.70 (m, 1H), 7.59 (m, 3H), 7.28 (m, 4H), 6.95 (d, J=8 Hz, 1H), 6.83 (dd, J=1/5 and 8 Hz, 1H), 6.40 (bs, 2H), 5.22 (dd, J=6.5 and 13 Hz, 1H), 4.00 (m, 1H), 3.71 (m, 1H), 3.34 (dd, J=1.5 and 8 Hz, 1H), 2.84 (s, 3H) ppm; ESI mass spectrum analysis m/z (relative intensity) 517 (M+H, 100).
  • 244. The following tables contain representative examples of the present invention. Each entry in each table is intended to be paired with each formulae at the start of the table. For example, in Table 1, example 1 is intended to be paired with each of formulae a-ttt and in Table 2, example 1 is intended to be paired with each of formulae a-ss.
  • 245. The following groups are intended for group A in the following tables.
    Figure US20010000179A1-20010405-C00025
    TABLE 1
  • 246.
    Ex # R1c A B
    1 CH3 phenyl 2-(aminosulfonyl)phenyl
    2 CH3 phenyl 2-(methylaminosulfonyl)phenyl
    3 CH3 phenyl 1-pyrrolidinocarbonyl
    4 CH3 phenyl 2-(methylsulfonyl)phenyl
    5 CH3 phenyl 4-morpholino
    6 CH3 phenyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    7 CH3 phenyl 4-morpholinocarbonyl
    8 CH3 phenyl 2-methyl-1-imidazolyl
    9 CH3 phenyl 5-methyl-1-imidazolyl
    10 CH3 phenyl 2-methylsulfonyl-1-imidazolyl
    11 CH3 2-pyridyl 2-(aminosulfonyl)phenyl
    12 CH3 2-pyridyl 2-(methylaminosulfonyl)phenyl
    13 CH3 2-pyridyl 1-pyrrolidinocarbonyl
    14 CH3 2-pyridyl 2-(methylsulfonyl)phenyl
    15 CH3 2-pyridyl 4-morpholino
    16 CH3 2-pyridyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    17 CH3 2-pyridyl 4-morpholinocarbonyl
    18 CH3 2-pyridyl 2-methyl-1-imidazolyl
    19 CH3 2-pyridyl 5-methyl-1-imidazolyl
    20 CH3 2-pyridyl 2-methylsulfonyl-1-imidazolyl
    21 CH3 3-pyridyl 2-(aminosulfonyl)phenyl
    22 CH3 3-pyridyl 2-(methylaminosulfonyl)phenyl
    23 CH3 3-pyridyl 1-pyrrolidinocarbonyl
    24 CH3 3-pyridyl 2-(methylsulfonyl)phenyl
    25 CH3 3-pyridyl 4-morpholino
    26 CH3 3-pyridyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    27 CH3 3-pyridyl 4-morpholinocarbonyl
    28 CH3 3-pyridyl 2-methyl-1-imidazolyl
    29 CH3 3-pyridyl 5-methyl-1-imidazolyl
    30 CH3 3-pyridyl 2-methylsulfonyl-1-imidazolyl
    31 CH3 2-pyrimidyl 2-(aminosulfonyl)phenyl
    32 CH3 2-pyrimidyl 2-(methylaminosulfonyl)phenyl
    33 CH3 2-pyrimidyl 1-pyrrolidinocarbonyl
    34 CH3 2-pyrimidyl 2-(methylsulfonyl)phenyl
    35 CH3 2-pyrimidyl 4-morpholino
    36 CH3 2-pyrimidyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    37 CH3 2-pyrimidyl 4-morpholinocarbonyl
    38 CH3 2-pyrimidyl 2-methyl-1-imidazolyl
    39 CH3 2-pyrimidyl 5-methyl-1-imidazolyl
    40 CH3 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl
    41 CH3 5-pyrimidyl 2-(aminosulfonyl)phenyl
    42 CH3 5-pyrimidyl 2-(methylaminosulfonyl)phenyl
    43 CH3 5-pyrimidyl 1-pyrrolidinocarbonyl
    44 CH3 5-pyrimidyl 2-(methylsulfonyl)phenyl
    45 CH3 5-pyrimidyl 4-morpholino
    46 CH3 5-pyrimidyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    47 CH3 5-pyrimidyl 4-morpholinocarbonyl
    48 CH3 5-pyrimidyl 2-methyl-1-imidazolyl
    49 CH3 5-pyrimidyl 5-methyl-1-imidazolyl
    50 CH3 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl
    51 CH3 2-Cl-phenyl 2-(aminosulfonyl)phenyl
    52 CH3 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl
    53 CH3 2-Cl-phenyl 1-pyrrolidinocarbonyl
    54 CH3 2-Cl-phenyl 2-(methylsulfonyl)phenyl
    55 CH3 2-Cl-phenyl 4-morpholino
    56 CH3 2-Cl-phenyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    57 CH3 2-Cl-phenyl 4-morpholinocarbonyl
    58 CH3 2-Cl-phenyl 2-methyl-1-imidazolyl
    59 CH3 2-Cl-phenyl 5-methyl-1-imidazolyl
    60 CH3 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl
    61 CH3 2-F-phenyl 2-(aminosulfonyl)phenyl
    62 CH3 2-F-phenyl 2-(methylaminosulfonyl)phenyl
    63 CH3 2-F-phenyl 1-pyrrolidinocarbonyl
    64 CH3 2-F-phenyl 2-(methylsulfonyl)phenyl
    65 CH3 2-F-phenyl 4-morpholino
    66 CH3 2-F-phenyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    67 CH3 2-F-phenyl 4-morpholinocarbonyl
    68 CH3 2-F-phenyl 2-methyl-1-imidazolyl
    69 CH3 2-F-phenyl 5-methyl-1-imidazolyl
    70 CH3 2-F-phenyl 2-methylsulfonyl-1-imidazolyl
    71 CH3 2,6-diF-phenyl 2-(aminosulfonyl)phenyl
    72 CH3 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl
    73 CH3 2,6-diF-phenyl 1-pyrrolidinocarbonyl
    74 CH3 2,6-diF-phenyl 2-(methylsulfonyl)phenyl
    75 CH3 2,6-diF-phenyl 4-morpholino
    76 CH3 2,6-diF-phenyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    77 CH3 2,6-diF-phenyl 4-morpholinocarbonyl
    78 CH3 2,6-diF-phenyl 2-methyl-1-imidazolyl
    79 CH3 2,6-diF-phenyl 5-methyl-1-imidazolyl
    80 CH3 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl
    81 CH2CH3 phenyl 2-(aminosulfonyl)phenyl
    82 CH2CH3 phenyl 2-(methylaminosulfonyl)phenyl
    83 CH2CH3 phenyl 1-pyrrolidinocarbonyl
    84 CH2CH3 phenyl 2-(methylsulfonyl)phenyl
    85 CH2CH3 phenyl 4-morpholino
    86 CH2CH3 phenyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    87 CH2CH3 phenyl 4-morpholinocarbonyl
    88 CH2CH3 phenyl 2-methyl-1-imidazolyl
    89 CH2CH3 phenyl 5-methyl-1-imidazolyl
    90 CH2CH3 phenyl 2-methylsulfonyl-1-imidazolyl
    91 CH2CH3 2-pyridyl 2-(aminosulfonyl)phenyl
    92 CH2CH3 2-pyridyl 2-(methylaminosulfonyl)phenyl
    93 CH2CH3 2-pyridyl 1-pyrrolidinocarbonyl
    94 CH2CH3 2-pyridyl 2-(methylsulfonyl)phenyl
    95 CH2CH3 2-pyridyl 4-morpholino
    96 CH2CH3 2-pyridyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    97 CH2CH3 2-pyridyl 4-morpholinocarbonyl
    98 CH2CH3 2-pyridyl 2-methyl-1-imidazolyl
    99 CH2CH3 2-pyridyl 5-methyl-1-imidazolyl
    100 CH2CH3 2-pyridyl 2-methylsulfonyl-1-imidazolyl
    101 CH2CH3 3-pyridyl 2-(aminosulfonyl)phenyl
    102 CH2CH3 3-pyridyl 2-(methylaminosulfonyl)phenyl
    103 CH2CH3 3-pyridyl 1-pyrrolidinocarbonyl
    104 CH2CH3 3-pyridyl 2-(methylsulfonyl)phenyl
    105 CH2CH3 3-pyridyl 4-morpholino
    106 CH2CH3 3-pyridyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    107 CH2CH3 3-pyridyl 4-morpholinocarbonyl
    108 CH2CH3 3-pyridyl 2-methyl-1-imidazolyl
    109 CH2CH3 3-pyridyl 5-methyl-1-imidazolyl
    110 CH2CH3 3-pyridyl 2-methylsulfonyl-1-imidazolyl
    111 CH2CH3 2-pyrimidyl 2-(aminosulfonyl)phenyl
    112 CH2CH3 2-pyrimidyl 2-(methylaminosulfonyl)phenyl
    113 CH2CH3 2-pyrimidyl 1-pyrrolidinocarbonyl
    114 CH2CH3 2-pyrimidyl 2-(methylsulfonyl)phenyl
    115 CH2CH3 2-pyrimidyl 4-morpholino
    116 CH2CH3 2-pyrimidyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    117 CH2CH3 2-pyrimidyl 4-morpholinocarbonyl
    118 CH2CH3 2-pyrimidyl 2-methyl-1-imidazolyl
    119 CH2CH3 2-pyrimidyl 5-methyl-1-imidazolyl
    120 CH2CH3 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl
    121 CH2CH3 5-pyrimidyl 2-(aminosulfonyl)phenyl
    122 CH2CH3 5-pyrimidyl 2-(methylaminosulfonyl)phenyl
    123 CH2CH3 5-pyrimidyl 1-pyrrolidinocarbonyl
    124 CH2CH3 5-pyrimidyl 2-(methylsulfonyl)phenyl
    125 CH2CH3 5-pyrimidyl 4-morpholino
    126 CH2CH3 5-pyrimidyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    127 CH2CH3 5-pyrimidyl 4-morpholinocarbonyl
    128 CH2CH3 5-pyrimidyl 2-methyl-1-imidazolyl
    129 CH2CH3 5-pyrimidyl 5-methyl-1-imidazolyl
    130 CH2CH3 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl
    131 CH2CH3 2-Cl-phenyl 2-(aminosulfonyl)phenyl
    132 CH2CH3 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl
    133 CH2CH3 2-Cl-phenyl 1-pyrrolidinocarbonyl
    134 CH2CH3 2-Cl-phenyl 2-(methylsulfonyl)phenyl
    135 CH2CH3 2-Cl-phenyl 4-morpholino
    136 CH2CH3 2-Cl-phenyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    137 CH2CH3 2-Cl-phenyl 4-morpholinocarbonyl
    138 CH2CH3 2-Cl-phenyl 2-methyl-1-imidazolyl
    139 CH2CH3 2-Cl-phenyl 5-methyl-1-imidazolyl
    140 CH2CH3 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl
    141 CH2CH3 2-F-phenyl 2-(aminosulfonyl)phenyl
    142 CH2CH3 2-F-phenyl 2-(methylaminosulfonyl)phenyl
    143 CH2CH3 2-F-phenyl 1-pyrrolidinocarbonyl
    144 CH2CH3 2-F-phenyl 2-(methylsulfonyl)phenyl
    145 CH2CH3 2-F-phenyl 4-morpholino
    146 CH2CH3 2-F-phenyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    147 CH2CH3 2-F-phenyl 4-morpholinocarbonyl
    148 CH2CH3 2-F-phenyl 2-methyl-1-imidazolyl
    149 CH2CH3 2-F-phenyl 5-methyl-1-imidazolyl
    150 CH2CH3 2-F-phenyl 2-methylsulfonyl-1-imidazolyl
    151 CH2CH3 2,6-diF-phenyl 2-(aminosulfonyl)phenyl
    152 CH2CH3 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl
    153 CH2CH3 2,6-diF-phenyl 1-pyrrolidinocarbonyl
    154 CH2CH3 2,6-diF-phenyl 2-(methylsulfonyl)phenyl
    155 CH2CH3 2,6-diF-phenyl 4-morpholino
    156 CH2CH3 2,6-diF-phenyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    157 CH2CH3 2,6-diF-phenyl 4-morpholinocarbonyl
    158 CH2CH3 2,6-diF-phenyl 2-methyl-1-imidazolyl
    159 CH2CH3 2,6-diF-phenyl 5-methyl-1-imidazolyl
    160 CH2CH3 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl
    161 CF3 phenyl 2-(aminosulfonyl)phenyl
    162 CF3 phenyl 2-(methylaminosulfonyl)phenyl
    163 CF3 phenyl 1-pyrrolidinocarbonyl
    164 CF3 phenyl 2-(methylsulfonyl)phenyl
    165 CF3 phenyl 4-morpholino
    166 CF3 phenyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    167 CF3 phenyl 4-morpholinocarbonyl
    168 CF3 phenyl 2-methyl-1-imidazolyl
    169 CF3 phenyl 5-methyl-1-imidazolyl
    170 CF3 phenyl 2-methylsulfonyl-1-imidazolyl
    171 CF3 2-pyridyl 2-(aminosulfonyl)phenyl
    172 CF3 2-pyridyl 2-(methylaminosulfonyl)phenyl
    173 CF3 2-pyridyl 1-pyrrolidinocarbonyl
    174 CF3 2-pyridyl 2-(methylsulfonyl)phenyl
    175 CF3 2-pyridyl 4-morpholino
    176 CF3 2-pyridyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    177 CF3 2-pyridyl 4-morpholinocarbonyl
    178 CF3 2-pyridyl 2-methyl-1-imidazolyl
    179 CF3 2-pyridyl 5-methyl-1-imidazolyl
    180 CF3 2-pyridyl 2-methylsulfonyl-1-imidazolyl
    181 CF3 3-pyridyl 2-(aminosulfonyl)phenyl
    182 CF3 3-pyridyl 2-(methylaminosulfonyl)phenyl
    183 CF3 3-pyridyl 1-pyrrolidinocarbonyl
    184 CF3 3-pyridyl 2-(methylsulfonyl)phenyl
    185 CF3 3-pyridyl 4-morpholino
    186 CF3 3-pyridyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    187 CF3 3-pyridyl 4-morpholinocarbonyl
    188 CF3 3-pyridyl 2-methyl-1-imidazolyl
    189 CF3 3-pyridyl 5-methyl-1-imidazolyl
    190 CF3 3-pyridyl 2-methylsulfonyl-1-imidazolyl
    191 CF3 2-pyrimidyl 2-(aminosulfonyl)phenyl
    192 CF3 2-pyrimidyl 2-(methylaminosulfonyl)phenyl
    193 CF3 2-pyrimidyl 1-pyrrolidinocarbonyl
    194 CF3 2-pyrimidyl 2-(methylsulfonyl)phenyl
    195 CF3 2-pyrimidyl 4-morpholino
    196 CF3 2-pyrimidyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    197 CF3 2-pyrimidyl 4-morpholinocarbonyl
    198 CF3 2-pyrimidyl 2-methyl-1-imidazolyl
    199 CF3 2-pyrimidyl 5-methyl-1-imidazolyl
    200 CF3 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl
    201 CF3 5-pyrimidyl 2-(aminosulfonyl)phenyl
    202 CF3 5-pyrimidyl 2-(methylaminosulfonyl)phenyl
    203 CF3 5-pyrimidyl 1-pyrrolidinocarbonyl
    204 CF3 5-pyrimidyl 2-(methylsulfonyl)phenyl
    205 CF3 5-pyrimidyl 4-morpholino
    206 CF3 5-pyrimidyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    207 CF3 5-pyrimidyl 4-morpholinocarbonyl
    208 CF3 5-pyrimidyl 2-methyl-1-imidazolyl
    209 CF3 5-pyrimidyl 5-methyl-1-imidazolyl
    210 CF3 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl
    211 CF3 2-Cl-phenyl 2-(aminosulfonyl)phenyl
    212 CF3 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl
    213 CF3 2-Cl-phenyl 1-pyrrolidinocarbonyl
    214 CF3 2-Cl-phenyl 2-(methylsulfonyl)phenyl
    215 CF3 2-Cl-phenyl 4-morpholino
    216 CF3 2-Cl-phenyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    217 CF3 2-Cl-phenyl 4-morpholinocarbonyl
    218 CF3 2-Cl-phenyl 2-methyl-1-imidazolyl
    219 CF3 2-Cl-phenyl 5-methyl-1-imidazolyl
    220 CF3 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl
    221 CF3 2-F-phenyl 2-(aminosulfonyl)phenyl
    222 CF3 2-F-phenyl 2-(methylaminosulfonyl)phenyl
    223 CF3 2-F-phenyl 1-pyrrolidinocarbonyl
    224 CF3 2-F-phenyl 2-(methylsulfonyl)phenyl
    225 CF3 2-F-phenyl 4-morpholino
    226 CF3 2-F-phenyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    227 CF3 2-F-phenyl 4-morpholinocarbonyl
    228 CF3 2-F-phenyl 2-methyl-1-imidazolyl
    229 CF3 2-F-phenyl 5-methyl-1-imidazolyl
    230 CF3 2-F-phenyl 2-methylsulfonyl-1-imidazolyl
    231 CF3 2,6-diF-phenyl 2-(aminosulfonyl)phenyl
    232 CF3 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl
    233 CF3 2,6-diF-phenyl 1-pyrrolidinocarbonyl
    234 CF3 2,6-diF-phenyl 2-(methylsulfonyl)phenyl
    235 CF3 2,6-diF-phenyl 4-morpholino
    236 CF3 2,6-diF-phenyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    237 CF3 2,6-diF-phenyl 4-morpholinocarbonyl
    238 CF3 2,6-diF-phenyl 2-methyl-1-imidazolyl
    239 CF3 2,6-diF-phenyl 5-methyl-1-imidazolyl
    240 CF3 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl
    241 SCH3 phenyl 2-(aminosulfonyl)phenyl
    242 SCH3 phenyl 2-(methylaminosulfonyl)phenyl
    243 SCH3 phenyl 1-pyrrolidinocarbonyl
    244 SCH3 phenyl 2-(methylsulfonyl)phenyl
    245 SCH3 phenyl 4-morpholino
    246 SCH3 phenyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    247 SCH3 phenyl 4-morpholinocarbonyl
    248 SCH3 phenyl 2-methyl-1-imidazolyl
    249 SCH3 phenyl 5-methyl-1-imidazolyl
    250 SCH3 phenyl 2-methylsulfonyl-1-imidazolyl
    251 SCH3 2-pyridyl 2-(aminosulfonyl)phenyl
    252 SCH3 2-pyridyl 2-(methylaminosulfonyl)phenyl
    253 SCH3 2-pyridyl 1-pyrrolidinocarbonyl
    254 SCH3 2-pyridyl 2-(methylsulfonyl)phenyl
    255 SCH3 2-pyridyl 4-morpholino
    256 SCH3 2-pyridyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    257 SCH3 2-pyridyl 4-morpholinocarbonyl
    258 SCH3 2-pyridyl 2-methyl-1-imidazolyl
    259 SCH3 2-pyridyl 5-methyl-1-imidazolyl
    260 SCH3 2-pyridyl 2-methylsulfonyl-1-imidazolyl
    261 SCH3 3-pyridyl 2-(aminosulfonyl)phenyl
    262 SCH3 3-pyridyl 2-(methylaminosulfonyl)phenyl
    263 SCH3 3-pyridyl 1-pyrrolidinocarbonyl
    264 SCH3 3-pyridyl 2-(methylsulfonyl)phenyl
    265 SCH3 3-pyridyl 4-morpholino
    266 SCH3 3-pyridyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    267 SCH3 3-pyridyl 4-morpholinocarbonyl
    268 SCH3 3-pyridyl 2-methyl-1-imidazolyl
    269 SCH3 3-pyridyl 5-methyl-1-imidazolyl
    270 SCH3 3-pyridyl 2-methylsulfonyl-1-imidazolyl
    271 SCH3 2-pyrimidyl 2-(aminosulfonyl)phenyl
    272 SCH3 2-pyrimidyl 2-(methylaminosulfonyl)phenyl
    273 SCH3 2-pyrimidyl 1-pyrrolidinocarbonyl
    274 SCH3 2-pyrimidyl 2-(methylsulfonyl)phenyl
    275 SCH3 2-pyrimidyl 4-morpholino
    276 SCH3 2-pyrimidyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    277 SCH3 2-pyrimidyl 4-morpholinocarbonyl
    278 SCH3 2-pyrimidyl 2-methyl-1-imidazolyl
    279 SCH3 2-pyrimidyl 5-methyl-1-imidazolyl
    280 SCH3 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl
    281 SCH3 5-pyrimidyl 2-(aminosulfonyl)phenyl
    282 SCH3 5-pyrimidyl 2-(methylaminosulfonyl)phenyl
    283 SCH3 5-pyrimidyl 1-pyrrolidinocarbonyl
    284 SCH3 5-pyrimidyl 2-(methylsulfonyl)phenyl
    285 SCH3 5-pyrimidyl 4-morpholino
    286 SCH3 5-pyrimidyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    287 SCH3 5-pyrimidyl 4-morpholinocarbonyl
    288 SCH3 5-pyrimidyl 2-methyl-1-imidazolyl
    289 SCH3 5-pyrimidyl 5-methyl-1-imidazolyl
    290 SCH3 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl
    291 SCH3 2-Cl-phenyl 2-(aminosulfonyl)phenyl
    292 SCH3 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl
    293 SCH3 2-Cl-phenyl 1-pyrrolidinocarbonyl
    294 SCH3 2-Cl-phenyl 2-(methylsulfonyl)phenyl
    295 SCH3 2-Cl-phenyl 4-morpholino
    296 SCH3 2-Cl-phenyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    297 SCH3 2-Cl-phenyl 4-morpholinocarbonyl
    298 SCH3 2-Cl-phenyl 2-methyl-1-imidazolyl
    299 SCH3 2-Cl-phenyl 5-methyl-1-imidazolyl
    300 SCH3 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl
    301 SCH3 2-F-phenyl 2-(aminosulfonyl)phenyl
    302 SCH3 2-F-phenyl 2-(methylaminosulfonyl)phenyl
    303 SCH3 2-F-phenyl 1-pyrrolidinocarbonyl
    304 SCH3 2-F-phenyl 2-(methylsulfonyl)phenyl
    305 SCH3 2-F-phenyl 4-morpholino
    306 SCH3 2-F-phenyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    307 SCH3 2-F-phenyl 4-morpholinocarbonyl
    308 SCH3 2-F-phenyl 2-methyl-1-imidazolyl
    309 SCH3 2-F-phenyl 5-methyl-1-imidazolyl
    310 SCH3 2-F-phenyl 2-methylsulfonyl-1-imidazolyl
    311 SCH3 2,6-diF-phenyl 2-(aminosulfonyl)phenyl
    312 SCH3 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl
    313 SCH3 2,6-diF-phenyl 1-pyrrolidinocarbonyl
    314 SCH3 2,6-diF-phenyl 2-(methylsulfonyl)phenyl
    315 SCH3 2,6-diF-phenyl 4-morpholino
    316 SCH3 2,6-diF-phenyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    317 SCH3 2,6-diF-phenyl 4-morpholinocarbonyl
    318 SCH3 2,6-diF-phenyl 2-methyl-1-imidazolyl
    319 SCH3 2,6-diF-phenyl 5-methyl-1-imidazolyl
    320 SCH3 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl
    321 SOCH3 phenyl 2-(aminosulfonyl)phenyl
    322 SOCH3 phenyl 2-(methylaminosulfonyl)phenyl
    323 SOCH3 phenyl 1-pyrrolidinocarbonyl
    324 SOCH3 phenyl 2-(methylsulfonyl)phenyl
    325 SOCH3 phenyl 4-morpholino
    326 SOCH3 phenyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    327 SOCH3 phenyl 4-morpholinocarbonyl
    328 SOCH3 phenyl 2-methyl-1-imidazolyl
    329 SOCH3 phenyl 5-methyl-1-imidazolyl
    330 SOCH3 phenyl 2-methylsulfonyl-1-imidazolyl
    331 SOCH3 2-pyridyl 2-(aminosulfonyl)phenyl
    332 SOCH3 2-pyridyl 2-(methylaminosulfonyl)phenyl
    333 SOCH3 2-pyridyl 1-pyrrolidinocarbonyl
    334 SOCH3 2-pyridyl 2-(methylsulfonyl)phenyl
    335 SOCH3 2-pyridyl 4-morpholino
    336 SOCH3 2-pyridyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    337 SOCH3 2-pyridyl 4-morpholinocarbonyl
    338 SOCH3 2-pyridyl 2-methyl-1-imidazolyl
    339 SOCH3 2-pyridyl 5-methyl-1-imidazolyl
    340 SOCH3 2-pyridyl 2-methylsulfonyl-1-imidazolyl
    341 SOCH3 3-pyridyl 2-(aminosulfonyl)phenyl
    342 SOCH3 3-pyridyl 2-(methylaminosulfonyl)phenyl
    343 SOCH3 3-pyridyl 1-pyrrolidinocarbonyl
    344 SOCH3 3-pyridyl 2-(methylsulfonyl)phenyl
    345 SOCH3 3-pyridyl 4-morpholino
    346 SOCH3 3-pyridyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    347 SOCH3 3-pyridyl 4-morpholinocarbonyl
    348 SOCH3 3-pyridyl 2-methyl-1-imidazolyl
    349 SOCH3 3-pyridyl 5-methyl-1-imidazolyl
    350 SOCH3 3-pyridyl 2-methylsulfonyl-1-imidazolyl
    351 SOCH3 2-pyrimidyl 2-(aminosulfonyl)phenyl
    352 SOCH3 2-pyrimidyl 2-(methylaminosulfonyl)phenyl
    353 SOCH3 2-pyrimidyl 1-pyrrolidinocarbonyl
    354 SOCH3 2-pyrimidyl 2-(methylsulfonyl)phenyl
    355 SOCH3 2-pyrimidyl 4-morpholino
    356 SOCH3 2-pyrimidyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    357 SOCH3 2-pyrimidyl 4-morpholinocarbonyl
    358 SOCH3 2-pyrimidyl 2-methyl-1-imidazolyl
    359 SOCH3 2-pyrimidyl 5-methyl-1-imidazolyl
    360 SOCH3 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl
    361 SOCH3 5-pyrimidyl 2-(aminosulfonyl)phenyl
    362 SOCH3 5-pyrimidyl 2-(methylaminosulfonyl)phenyl
    363 SOCH3 5-pyrimidyl 1-pyrrolidinocarbonyl
    364 SOCH3 5-pyrimidyl 2-(methylsulfonyl)phenyl
    365 SOCH3 5-pyrimidyl 4-morpholino
    366 SOCH3 5-pyrimidyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    367 SOCH3 5-pyrimidyl 4-morpholinocarbonyl
    368 SOCH3 5-pyrimidyl 2-methyl-1-imidazolyl
    369 SOCH3 5-pyrimidyl 5-methyl-1-imidazolyl
    370 SOCH3 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl
    371 SOCH3 2-Cl-phenyl 2-(aminosulfonyl)phenyl
    372 SOCH3 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl
    373 SOCH3 2-Cl-phenyl 1-pyrrolidinocarbonyl
    374 SOCH3 2-Cl-phenyl 2-(methylsulfonyl)phenyl
    375 SOCH3 2-Cl-phenyl 4-morpholino
    376 SOCH3 2-Cl-phenyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    377 SOCH3 2-Cl-phenyl 4-morpholinocarbonyl
    378 SOCH3 2-Cl-phenyl 2-methyl-1-imidazolyl
    379 SOCH3 2-Cl-phenyl 5-methyl-1-imidazolyl
    380 SOCH3 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl
    381 SOCH3 2-F-phenyl 2-(aminosulfonyl)phenyl
    382 SOCH3 2-F-phenyl 2-(methylaminosulfonyl)phenyl
    383 SOCH3 2-F-phenyl 1-pyrrolidinocarbonyl
    384 SOCH3 2-F-phenyl 2-(methylsulfonyl)phenyl
    385 SOCH3 2-F-phenyl 4-morpholino
    386 SOCH3 2-F-phenyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    387 SOCH3 2-F-phenyl 4-morpholinocarbonyl
    388 SOCH3 2-F-phenyl 2-methyl-1-imidazolyl
    389 SOCH3 2-F-phenyl 5-methyl-1-imidazolyl
    390 SOCH3 2-F-phenyl 2-methylsulfonyl-1-imidazolyl
    391 SOCH3 2,6-diF-phenyl 2-(aminosulfonyl)phenyl
    392 SOCH3 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl
    393 SOCH3 2,6-diF-phenyl 1-pyrrolidinocarbonyl
    394 SOCH3 2,6-diF-phenyl 2-(methylsulfonyl)phenyl
    395 SOCH3 2,6-diF-phenyl 4-morpholino
    396 SOCH3 2,6-diF-phenyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    397 SOCH3 2,6-diF-phenyl 4-morpholinocarbonyl
    398 SOCH3 2,6-diF-phenyl 2-methyl-1-imidazolyl
    399 SOCH3 2,6-diF-phenyl 5-methyl-1-imidazolyl
    400 SOCH3 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl
    401 SO2CH3 phenyl 2-(aminosulfonyl)phenyl
    402 SO2CH3 phenyl 2-(methylaminosulfonyl)phenyl
    403 SO2CH3 phenyl 1-pyrrolidinocarbonyl
    404 SO2CH3 phenyl 2-(methylsulfonyl)phenyl
    405 SO2CH3 phenyl 4-morpholino
    406 SO2CH3 phenyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    407 SO2CH3 phenyl 4-morpholinocarbonyl
    408 SO2CH3 phenyl 2-methyl-1-imidazolyl
    409 SO2CH3 phenyl 5-methyl-1-imidazolyl
    410 SO2CH3 phenyl 2-methylsulfonyl-1-imidazolyl
    411 SO2CH3 2-pyridyl 2-(aminosulfonyl)phenyl
    412 SO2CH3 2-pyridyl 2-(methylaminosulfonyl)phenyl
    413 SO2CH3 2-pyridyl 1-pyrrolidinocarbonyl
    414 SO2CH3 2-pyridyl 2-(methylsulfonyl)phenyl
    415 SO2CH3 2-pyridyl 4-morpholino
    416 SO2CH3 2-pyridyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    417 SO2CH3 2-pyridyl 4-morpholinocarbonyl
    418 SO2CH3 2-pyridyl 2-methyl-1-imidazolyl
    419 SO2CH3 2-pyridyl 5-methyl-1-imidazolyl
    420 SO2CH3 2-pyridyl 2-methylsulfonyl-1-imidazolyl
    421 SO2CH3 3-pyridyl 2-(aminosulfonyl)phenyl
    422 SO2CH3 3-pyridyl 2-(methylaminosulfonyl)phenyl
    423 SO2CH3 3-pyridyl 1-pyrrolidinocarbonyl
    424 SO2CH3 3-pyridyl 2-(methylsulfonyl)phenyl
    425 SO2CH3 3-pyridyl 4-morpholino
    426 SO2CH3 3-pyridyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    427 SO2CH3 3-pyridyl 4-morpholinocarbonyl
    428 SO2CH3 3-pyridyl 2-methyl-1-imidazolyl
    429 SO2CH3 3-pyridyl 5-methyl-1-imidazolyl
    430 SO2CH3 3-pyridyl 2-methylsulfonyl-1-imidazolyl
    431 SO2CH3 2-pyrimidyl 2-(aminosulfonyl)phenyl
    432 SO2CH3 2-pyrimidyl 2-(methylaminosulfonyl)phenyl
    433 SO2CH3 2-pyrimidyl 1-pyrrolidinocarbonyl
    434 SO2CH3 2-pyrimidyl 2-(methylsulfonyl)phenyl
    435 SO2CH3 2-pyrimidyl 4-morpholino
    436 SO2CH3 2-pyrimidyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    437 SO2CH3 2-pyrimidyl 4-morpholinocarbonyl
    438 SO2CH3 2-pyrimidyl 2-methyl-1-imidazolyl
    439 SO2CH3 2-pyrimidyl 5-methyl-1-imidazolyl
    440 SO2CH3 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl
    441 SO2CH3 5-pyrimidyl 2-(aminosulfonyl)phenyl
    442 SO2CH3 5-pyrimidyl 2-(methylaminosulfonyl)phenyl
    443 SO2CH3 5-pyrimidyl 1-pyrrolidinocarbonyl
    444 SO2CH3 5-pyrimidyl 2-(methylsulfonyl)phenyl
    445 SO2CH3 5-pyrimidyl 4-morpholino
    446 SO2CH3 5-pyrimidyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    447 SO2CH3 5-pyrimidyl 4-morpholinocarbonyl
    448 SO2CH3 5-pyrimidyl 2-methyl-1-imidazolyl
    449 SO2CH3 5-pyrimidyl 5-methyl-1-imidazolyl
    450 SO2CH3 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl
    451 SO2CH3 2-Cl-phenyl 2-(aminosulfonyl)phenyl
    452 SO2CH3 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl
    453 SO2CH3 2-Cl-phenyl 1-pyrrolidinocarbonyl
    454 SO2CH3 2-Cl-phenyl 2-(methylsulfonyl)phenyl
    455 SO2CH3 2-Cl-phenyl 4-morpholino
    456 SO2CH3 2-Cl-phenyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    457 SO2CH3 2-Cl-phenyl 4-morpholinocarbonyl
    458 SO2CH3 2-Cl-phenyl 2-methyl-1-imidazolyl
    459 SO2CH3 2-Cl-phenyl 5-methyl-1-imidazolyl
    460 SO2CH3 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl
    461 SO2CH3 2-F-phenyl 2-(aminosulfonyl)phenyl
    462 SO2CH3 2-F-phenyl 2-(methylaminosulfonyl)phenyl
    463 SO2CH3 2-F-phenyl 1-pyrrolidinocarbonyl
    464 SO2CH3 2-F-phenyl 2-(methylsulfonyl)phenyl
    465 SO2CH3 2-F-phenyl 4-morpholino
    466 SO2CH3 2-F-phenyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    467 SO2CH3 2-F-phenyl 4-morpholinocarbonyl
    468 SO2CH3 2-F-phenyl 2-methyl-1-imidazolyl
    469 SO2CH3 2-F-phenyl 5-methyl-1-imidazolyl
    470 SO2CH3 2-F-phenyl 2-methylsulfonyl-1-imidazolyl
    471 SO2CH3 2,6-diF-phenyl 2-(aminosulfonyl)phenyl
    472 SO2CH3 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl
    473 SO2CH3 2,6-diF-phenyl 1-pyrrolidinocarbonyl
    474 SO2CH3 2,6-diF-phenyl 2-(methylsulfonyl)phenyl
    475 SO2CH3 2,6-diF-phenyl 4-morpholino
    476 SO2CH3 2,6-diF-phenyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    477 SO2CH3 2,6-diF-phenyl 4-morpholinocarbonyl
    478 SO2CH3 2,6-diF-phenyl 2-methyl-1-imidazolyl
    479 SO2CH3 2,6-diF-phenyl 5-methyl-1-imidazolyl
    480 SO2CH3 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl
    481 CH2NH— phenyl 2-(aminosulfonyl)phenyl
    SO2CH3
    482 CH2NH— phenyl 2-(methylaminosulfonyl)phenyl
    SO2CH3
    483 CH2NH— phenyl 1-pyrrolidinocarbonyl
    SO2CH3
    484 CH2NH— phenyl 2-(methylsulfonyl)phenyl
    SO2CH3
    485 CH2NH— phenyl 4-morpholino
    SO2CH3
    486 CH2NH— phenyl 2-(1′-CF3-tetrazol-2-
    SO2CH3 yl)phenyl
    487 CH2NH— phenyl 4-morpholinocarbonyl
    SO2CH3
    488 CH2NH— phenyl 2-methyl-1-imidazolyl
    SO2CH3
    489 CH2NH— phenyl 5-methyl-1-imidazolyl
    SO2CH3
    490 CH2NH— phenyl 2-methylsulfonyl-1-imidazolyl
    SO2CH3
    491 CH2NH— 2-pyridyl 2-(aminosulfonyl)phenyl
    SO2CH3
    492 CH2NH— 2-pyridyl 2-(methylaminosulfonyl)phenyl
    SO2CH3
    493 CH2NH— 2-pyridyl 1-pyrrolidinocarbonyl
    SO2CH3
    494 CH2NH— 2-pyridyl 2-(methylsulfonyl)phenyl
    SO2CH3
    495 CH2NH— 2-pyridyl 4-morpholino
    SO2CH3
    496 CH2NH— 2-pyridyl 2-(1′-CF3-tetrazol-2-
    SO2CH3 yl)phenyl
    497 CH2NH— 2-pyridyl 4-morpholinocarbonyl
    SO2CH3
    498 CH2NH— 2-pyridyl 2-methyl-1-imidazolyl
    SO2CH3
    499 CH2NH— 2-pyridyl 5-methyl-1-imidazolyl
    SO2CH3
    500 CH2NH— 2-pyridyl 2-methylsulfonyl-1-imidazolyl
    SO2CH3
    501 CH2NH— 3-pyridyl 2-(aminosulfonyl)phenyl
    SO2CH3
    502 CH2NH— 3-pyridyl 2-(methylaminosulfonyl)phenyl
    SO2CH3
    503 CH2NH— 3-pyridyl 1-pyrrolidinocarbonyl
    SO2CH3
    504 CH2NH— 3-pyridyl 2-(methylsulfonyl)phenyl
    SO2CH3
    505 CH2NH— 3-pyridyl 4-morpholino
    SO2CH3
    506 CH2NH— 3-pyridyl 2-(1′-CF3-tetrazol-2-
    SO2CH3 yl)phenyl
    507 CH2NH— 3-pyridyl 4-morpholinocarbonyl
    SO2CH3
    508 CH2NH— 3-pyridyl 2-methyl-1-imidazolyl
    SO2CH3
    509 CH2NH— 3-pyridyl 5-methyl-1-imidazolyl
    SO2CH3
    510 CH2NH— 3-pyridyl 2-methylsulfonyl-1-imidazolyl
    SO2CH3
    511 CH2NH— 2-pyrimidyl 2-(aminosulfonyl)phenyl
    SO2CH3
    512 CH2NH— 2-pyrimidyl 2-(methylaminosulfonyl)phenyl
    SO2CH3
    513 CH2NH— 2-pyrimidyl 1-pyrrolidinocarbonyl
    SO2CH3
    514 CH2NH— 2-pyrimidyl 2-(methylsulfonyl)phenyl
    SO2CH3
    515 CH2NH— 2-pyrimidyl 4-morpholino
    SO2CH3
    516 CH2NH— 2-pyrimidyl 2-(1′-CF3-tetrazol-2-
    SO2CH3 yl)phenyl
    517 CH2NH— 2-pyrimidyl 4-morpholinocarbonyl
    SO2CH3
    518 CH2NH— 2-pyrimidyl 2-methyl-1-imidazolyl
    SO2CH3
    519 CH2NH— 2-pyrimidyl 5-methyl-1-imidazolyl
    SO2CH3
    520 CH2NH— 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl
    SO2CH3
    521 CH2NH— 5-pyrimidyl 2-(aminosulfonyl)phenyl
    SO2CH3
    522 CH2NH— 5-pyrimidyl 2-(methylaminosulfonyl)phenyl
    SO2CH3
    523 CH2NH— 5-pyrimidyl 1-pyrrolidinocarbonyl
    SO2CH3
    524 CH2NH— 5-pyrimidyl 2-(methylsulfonyl)phenyl
    SO2CH3
    525 CH2NH— 5-pyrimidyl 4-morpholino
    SO2CH3
    526 CH2NH— 5-pyrimidyl 2-(1′-CF3-tetrazol-2-
    SO2CH3 yl)phenyl
    527 CH2NH— 5-pyrimidyl 4-morpholinocarbonyl
    SO2CH3
    528 CH2NH— 5-pyrimidyl 2-methyl-1-imidazolyl
    SO2CH3
    529 CH2NH— 5-pyrimidyl 5-methyl-1-imidazolyl
    SO2CH3
    530 CH2NH— 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl
    SO2CH3
    531 CH2NH— 2-Cl-phenyl 2-(aminosulfonyl)phenyl
    SO2CH3
    532 CH2NH— 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl
    SO2CH3
    533 CH2NH— 2-Cl-phenyl 1-pyrrolidinocarbonyl
    SO2CH3
    534 CH2NH— 2-Cl-phenyl 2-(methylsulfonyl)phenyl
    SO2CH3
    535 CH2NH— 2-Cl-phenyl 4-morpholino
    SO2CH3
    536 CH2NH— 2-Cl-phenyl 2-(1′-CF3-tetrazol-2-
    SO2CH3 yl)phenyl
    537 CH2NH— 2-Cl-phenyl 4-morpholinocarbonyl
    SO2CH3
    538 CH2NH— 2-Cl-phenyl 2-methyl-1-imidazolyl
    SO2CH3
    539 CH2NH— 2-Cl-phenyl 5-methyl-1-imidazolyl
    SO2CH3
    540 CH2NH— 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl
    SO2CH3
    541 CH2NH— 2-F-phenyl 2-(aminosulfonyl)phenyl
    SO2CH3
    542 CH2NH— 2-F-phenyl 2-(methylaminosulfonyl)phenyl
    SO2CH3
    543 CH2NH— 2-F-phenyl 1-pyrrolidinocarbonyl
    SO2CH3
    544 CH2NH— 2-F-phenyl 2-(methylsulfonyl)phenyl
    SO2CH3
    545 CH2NH— 2-F-phenyl 4-morpholino
    SO2CH3
    546 CH2NH— 2-F-phenyl 2-(1′-CF3-tetrazol-2-
    SO2CH3 yl)phenyl
    547 CH2NH— 2-F-phenyl 4-morpholinocarbonyl
    SO2CH3
    548 CH2NH— 2-F-phenyl 2-methyl-1-imidazolyl
    SO2CH3
    549 CH2NH— 2-F-phenyl 5-methyl-1-imidazolyl
    SO2CH3
    550 CH2NH— 2-F-phenyl 2-methylsulfonyl-1-imidazolyl
    SO2CH3
    551 CH2NH— 2,6-diF-phenyl 2-(aminosulfonyl)phenyl
    SO2CH3
    552 CH2NH— 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl
    SO2CH3
    553 CH2NH— 2,6-diF-phenyl 1-pyrrolidinocarbonyl
    SO2CH3
    554 CH2NH— 2,6-diF-phenyl 2-(methylsulfonyl)phenyl
    SO2CH3
    555 CH2NH— 2,6-diF-phenyl 4-morpholino
    SO2CH3
    556 CH2NH— 2,6-diF-phenyl 2-(1′-CF3-tetrazol-2-
    SO2CH3 yl)phenyl
    557 CH2NH— 2,6-diF-phenyl 4-morpholinocarbonyl
    SO2CH3
    558 CH2NH— 2,6-diF-phenyl 2-methyl-1-imidazolyl
    SO2CH3
    559 CH2NH— 2,6-diF-phenyl 5-methyl-1-imidazolyl
    SO2CH3
    560 CH2NH— 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl
    SO2CH3
    561 Cl phenyl 2-(aminosulfonyl)phenyl
    562 Cl phenyl 2-(methylaminosulfonyl)phenyl
    563 Cl phenyl 1-pyrrolidinocarbonyl
    564 Cl phenyl 2-(methylsulfonyl)phenyl
    565 Cl phenyl 4-morpholino
    566 Cl phenyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    567 Cl phenyl 4-morpholinocarbonyl
    568 Cl phenyl 2-methyl-1-imidazolyl
    569 Cl phenyl 5-methyl-1-imidazolyl
    570 Cl phenyl 2-methylsulfonyl-1-imidazolyl
    571 Cl 2-pyridyl 2-(aminosulfonyl)phenyl
    572 Cl 2-pyridyl 2-(methylaminosulfonyl)phenyl
    573 Cl 2-pyridyl 1-pyrrolidinocarbonyl
    574 Cl 2-pyridyl 2-(methylsulfonyl)phenyl
    575 Cl 2-pyridyl 4-morpholino
    576 Cl 2-pyridyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    577 Cl 2-pyridyl 4-morpholinocarbonyl
    578 Cl 2-pyridyl 2-methyl-1-imidazolyl
    579 Cl 2-pyridyl 5-methyl-1-imidazolyl
    580 Cl 2-pyridyl 2-methylsulfonyl-1-imidazolyl
    581 Cl 3-pyridyl 2-(aminosulfonyl)phenyl
    582 Cl 3-pyridyl 2-(methylaminosulfonyl)phenyl
    583 Cl 3-pyridyl 1-pyrrolidinocarbonyl
    584 Cl 3-pyridyl 2-(methylsulfonyl)phenyl
    585 Cl 3-pyridyl 4-morpholino
    586 Cl 3-pyridyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    587 Cl 3-pyridyl 4-morpholinocarbonyl
    588 Cl 3-pyridyl 2-methyl-1-imidazolyl
    589 Cl 3-pyridyl 5-methyl-1-imidazolyl
    590 Cl 3-pyridyl 2-methylsulfonyl-1-imidazolyl
    591 Cl 2-pyrimidyl 2-(aminosulfonyl)phenyl
    592 Cl 2-pyrimidyl 2-(methylaminosulfonyl)phenyl
    593 Cl 2-pyrimidyl 1-pyrrolidinocarbonyl
    594 Cl 2-pyrimidyl 2-(methylsulfonyl)phenyl
    595 Cl 2-pyrimidyl 4-morpholino
    596 Cl 2-pyrimidyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    597 Cl 2-pyrimidyl 4-morpholinocarbonyl
    598 Cl 2-pyrimidyl 2-methyl-1-imidazolyl
    599 Cl 2-pyrimidyl 5-methyl-1-imidazolyl
    600 Cl 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl
    601 Cl 5-pyrimidyl 2-(aminosulfonyl)phenyl
    602 Cl 5-pyrimidyl 2-(methylaminosulfonyl)phenyl
    603 Cl 5-pyrimidyl 1-pyrrolidinocarbonyl
    604 Cl 5-pyrimidyl 2-(methylsulfonyl)phenyl
    605 Cl 5-pyrimidyl 4-morpholino
    606 Cl 5-pyrimidyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    607 Cl 5-pyrimidyl 4-morpholinocarbonyl
    608 Cl 5-pyrimidyl 2-methyl-1-imidazolyl
    609 Cl 5-pyrimidyl 5-methyl-1-imidazolyl
    610 Cl 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl
    611 Cl 2-Cl-phenyl 2-(aminosulfonyl)phenyl
    612 Cl 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl
    613 Cl 2-Cl-phenyl 1-pyrrolidinocarbonyl
    614 Cl 2-Cl-phenyl 2-(methylsulfonyl)phenyl
    615 Cl 2-Cl-phenyl 4-morpholino
    616 Cl 2-Cl-phenyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    617 Cl 2-Cl-phenyl 4-morpholinocarbonyl
    618 Cl 2-Cl-phenyl 2-methyl-1-imidazolyl
    619 Cl 2-Cl-phenyl 5-methyl-1-imidazolyl
    620 Cl 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl
    621 Cl 2-F-phenyl 2-(aminosulfonyl)phenyl
    622 Cl 2-F-phenyl 2-(methylaminosulfonyl)phenyl
    623 Cl 2-F-phenyl 1-pyrrolidinocarbonyl
    624 Cl 2-F-phenyl 2-(methylsulfonyl)phenyl
    625 Cl 2-F-phenyl 4-morpholino
    626 Cl 2-F-phenyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    627 Cl 2-F-phenyl 4-morpholinocarbonyl
    628 Cl 2-F-phenyl 2-methyl-1-imidazolyl
    629 Cl 2-F-phenyl 5-methyl-1-imidazolyl
    630 Cl 2-F-phenyl 2-methylsulfonyl-1-imidazolyl
    631 Cl 2,6-diF-phenyl 2-(aminosulfonyl)phenyl
    632 Cl 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl
    633 Cl 2,6-diF-phenyl 1-pyrrolidinocarbonyl
    634 Cl 2,6-diF-phenyl 2-(methylsulfonyl)phenyl
    635 Cl 2,6-diF-phenyl 4-morpholino
    636 Cl 2,6-diF-phenyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    637 Cl 2,6-diF-phenyl 4-morpholinocarbonyl
    638 Cl 2,6-diF-phenyl 2-methyl-1-imidazolyl
    639 Cl 2,6-diF-phenyl 5-methyl-1-imidazolyl
    640 Cl 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl
    641 F phenyl 2-(aminosulfonyl)phenyl
    642 F phenyl 2-(methylaminosulfonyl)phenyl
    643 F phenyl 1-pyrrolidinocarbonyl
    644 F phenyl 2-(methylsulfonyl)phenyl
    645 F phenyl 4-morpholino
    646 F phenyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    647 F phenyl 4-morpholinocarbonyl
    648 F phenyl 2-methyl-1-imidazolyl
    649 F phenyl 5-methyl-1-imidazolyl
    650 F phenyl 2-methylsulfonyl-1-imidazolyl
    651 F 2-pyridyl 2-(aminosulfonyl)phenyl
    652 F 2-pyridyl 2-(methylaminosulfonyl)phenyl
    653 F 2-pyridyl 1-pyrrolidinocarbonyl
    654 F 2-pyridyl 2-(methylsulfonyl)phenyl
    655 F 2-pyridyl 4-morpholino
    656 F 2-pyridyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    657 F 2-pyridyl 4-morpholinocarbonyl
    658 F 2-pyridyl 2-methyl-1-imidazolyl
    659 F 2-pyridyl 5-methyl-1-imidazolyl
    660 F 2-pyridyl 2-methylsulfonyl-1-imidazolyl
    661 F 3-pyridyl 2-(aminosulfonyl)phenyl
    662 F 3-pyridyl 2-(methylaminosulfonyl)phenyl
    663 F 3-pyridyl 1-pyrrolidinocarbonyl
    664 F 3-pyridyl 2-(methylsulfonyl)phenyl
    665 F 3-pyridyl 4-morpholino
    666 F 3-pyridyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    667 F 3-pyridyl 4-morpholinocarbonyl
    668 F 3-pyridyl 2-methyl-1-imidazolyl
    669 F 3-pyridyl 5-methyl-1-imidazolyl
    670 F 3-pyridyl 2-methylsulfonyl-1-imidazolyl
    671 F 2-pyrimidyl 2-(aminosulfonyl)phenyl
    672 F 2-pyrimidyl 2-(methylaminosulfonyl)phenyl
    673 F 2-pyrimidyl 1-pyrrolidinocarbonyl
    674 F 2-pyrimidyl 2-(methylsulfonyl)phenyl
    675 F 2-pyrimidyl 4-morpholino
    676 F 2-pyrimidyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    677 F 2-pyrimidyl 4-morpholinocarbonyl
    678 F 2-pyrimidyl 2-methyl-1-imidazolyl
    679 F 2-pyrimidyl 5-methyl-1-imidazolyl
    680 F 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl
    681 F 5-pyrimidyl 2-(aminosulfonyl)phenyl
    682 F 5-pyrimidyl 2-(methylaminosulfonyl)phenyl
    683 F 5-pyrimidyl 1-pyrrolidinocarbonyl
    684 F 5-pyrimidyl 2-(methylsulfonyl)phenyl
    685 F 5-pyrimidyl 4-morpholino
    686 F 5-pyrimidyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    687 F 5-pyrimidyl 4-morpholinocarbonyl
    688 F 5-pyrimidyl 2-methyl-1-imidazolyl
    689 F 5-pyrimidyl 5-methyl-1-imidazolyl
    690 F 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl
    691 F 2-Cl-phenyl 2-(aminosulfonyl)phenyl
    692 F 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl
    693 F 2-Cl-phenyl 1-pyrrolidinocarbonyl
    694 F 2-Cl-phenyl 2-(methylsulfonyl)phenyl
    695 F 2-Cl-phenyl 4-morpholino
    696 F 2-Cl-phenyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    697 F 2-Cl-phenyl 4-morpholinocarbonyl
    698 F 2-Cl-phenyl 2-methyl-1-imidazolyl
    699 F 2-Cl-phenyl 5-methyl-1-imidazolyl
    700 F 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl
    701 F 2-F-phenyl 2-(aminosulfonyl)phenyl
    702 F 2-F-phenyl 2-(methylaminosulfonyl)phenyl
    703 F 2-F-phenyl 1-pyrrolidinocarbonyl
    704 F 2-F-phenyl 2-(methylsulfonyl)phenyl
    705 F 2-F-phenyl 4-morpholino
    706 F 2-F-phenyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    707 F 2-F-phenyl 4-morpholinocarbonyl
    708 F 2-F-phenyl 2-methyl-1-imidazolyl
    709 F 2-F-phenyl 5-methyl-1-imidazolyl
    710 F 2-F-phenyl 2-methylsulfonyl-1-imidazolyl
    711 F 2,6-diF-phenyl 2-(aminosulfonyl)phenyl
    712 F 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl
    713 F 2,6-diF-phenyl 1-pyrrolidinocarbonyl
    714 F 2,6-diF-phenyl 2-(methylsulfonyl)phenyl
    715 F 2,6-diF-phenyl 4-morpholino
    716 F 2,6-diF-phenyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    717 F 2,6-diF-phenyl 4-morpholinocarbonyl
    718 F 2,6-diF-phenyl 2-methyl-1-imidazolyl
    719 F 2,6-diF-phenyl 5-methyl-1-imidazolyl
    720 F 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl
    721 CO2CH3 phenyl 2-(aminosulfonyl)phenyl
    722 CO2CH3 phenyl 2-(methylaminosulfonyl)phenyl
    723 CO2CH3 phenyl 1-pyrrolidinocarbonyl
    724 CO2CH3 phenyl 2-(methylsulfonyl)phenyl
    725 CO2CH3 phenyl 4-morpholino
    726 CO2CH3 phenyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    727 CO2CH3 phenyl 4-morpholinocarbonyl
    728 CO2CH3 phenyl 2-methyl-1-imidazolyl
    729 CO2CH3 phenyl 5-methyl-1-imidazolyl
    730 CO2CH3 phenyl 2-methylsulfonyl-1-imidazolyl
    731 CO2CH3 2-pyridyl 2-(aminosulfonyl)phenyl
    732 CO2CH3 2-pyridyl 2-(methylaminosulfonyl)phenyl
    733 CO2CH3 2-pyridyl 1-pyrrolidinocarbonyl
    734 CO2CH3 2-pyridyl 2-(methylsulfonyl)phenyl
    735 CO2CH3 2-pyridyl 4-morpholino
    736 CO2CH3 2-pyridyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    737 CO2CH3 2-pyridyl 4-morpholinocarbonyl
    738 CO2CH3 2-pyridyl 2-methyl-1-imidazolyl
    739 CO2CH3 2-pyridyl 5-methyl-1-imidazolyl
    740 CO2CH3 2-pyridyl 2-methylsulfonyl-1-imidazolyl
    741 CO2CH3 3-pyridyl 2-(aminosulfonyl)phenyl
    742 CO2CH3 3-pyridyl 2-(methylaminosulfonyl)phenyl
    743 CO2CH3 3-pyridyl 1-pyrrolidinocarbonyl
    744 CO2CH3 3-pyridyl 2-(methylsulfonyl)phenyl
    745 CO2CH3 3-pyridyl 4-morpholino
    746 CO2CH3 3-pyridyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    747 CO2CH3 3-pyridyl 4-morpholinocarbonyl
    748 CO2CH3 3-pyridyl 2-methyl-1-imidazolyl
    749 CO2CH3 3-pyridyl 5-methyl-1-imidazolyl
    750 CO2CH3 3-pyridyl 2-methylsulfonyl-1-imidazolyl
    751 CO2CH3 2-pyrimidyl 2-(aminosulfonyl)phenyl
    752 CO2CH3 2-pyrimidyl 2-(methylaminosulfonyl)phenyl
    753 CO2CH3 2-pyrimidyl 1-pyrrolidinocarbonyl
    754 CO2CH3 2-pyrimidyl 2-(methylsulfonyl)phenyl
    755 CO2CH3 2-pyrimidyl 4-morpholino
    756 CO2CH3 2-pyrimidyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    757 CO2CH3 2-pyrimidyl 4-morpholinocarbonyl
    758 CO2CH3 2-pyrimidyl 2-methyl-1-imidazolyl
    759 CO2CH3 2-pyrimidyl 5-methyl-1-imidazolyl
    760 CO2CH3 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl
    761 CO2CH3 5-pyrimidyl 2-(aminosulfonyl)phenyl
    762 CO2CH3 5-pyrimidyl 2-(methylaminosulfonyl)phenyl
    763 CO2CH3 5-pyrimidyl 1-pyrrolidinocarbonyl
    764 CO2CH3 5-pyrimidyl 2-(methylsulfonyl)phenyl
    765 CO2CH3 5-pyrimidyl 4-morpholino
    766 CO2CH3 5-pyrimidyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    767 CO2CH3 5-pyrimidyl 4-morpholinocarbonyl
    768 CO2CH3 5-pyrimidyl 2-methyl-1-imidazolyl
    769 CO2CH3 5-pyrimidyl 5-methyl-1-imidazolyl
    770 CO2CH3 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl
    771 CO2CH3 2-Cl-phenyl 2-(aminosulfonyl)phenyl
    772 CO2CH3 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl
    773 CO2CH3 2-Cl-phenyl 1-pyrrolidinocarbonyl
    774 CO2CH3 2-Cl-phenyl 2-(methylsulfonyl)phenyl
    775 CO2CH3 2-Cl-phenyl 4-morpholino
    776 CO2CH3 2-Cl-phenyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    777 CO2CH3 2-Cl-phenyl 4-morpholinocarbonyl
    778 CO2CH3 2-Cl-phenyl 2-methyl-1-imidazolyl
    779 CO2CH3 2-Cl-phenyl 5-methyl-1-imidazolyl
    780 CO2CH3 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl
    781 CO2CH3 2-F-phenyl 2-(aminosulfonyl)phenyl
    782 CO2CH3 2-F-phenyl 2-(methylaminosulfonyl)phenyl
    783 CO2CH3 2-F-phenyl 1-pyrrolidinocarbonyl
    784 CO2CH3 2-F-phenyl 2-(methylsulfonyl)phenyl
    785 CO2CH3 2-F-phenyl 4-morpholino
    786 CO2CH3 2-F-phenyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    787 CO2CH3 2-F-phenyl 4-morpholinocarbonyl
    788 CO2CH3 2-F-phenyl 2-methyl-1-imidazolyl
    789 CO2CH3 2-F-phenyl 5-methyl-1-imidazolyl
    790 CO2CH3 2-F-phenyl 2-methylsulfonyl-1-imidazolyl
    791 CO2CH3 2,6-diF-phenyl 2-(aminosulfonyl)phenyl
    792 CO2CH3 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl
    793 CO2CH3 2,6-diF-phenyl 1-pyrrolidinocarbonyl
    794 CO2CH3 2,6-diF-phenyl 2-(methylsulfonyl)phenyl
    795 CO2CH3 2,6-diF-phenyl 4-morpholino
    796 CO2CH3 2,6-diF-phenyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    797 CO2CH3 2,6-diF-phenyl 4-morpholinocarbonyl
    798 CO2CH3 2,6-diF-phenyl 2-methyl-1-imidazolyl
    799 CO2CH3 2,6-diF-phenyl 5-methyl-1-imidazolyl
    800 CO2CH3 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl
    801 CH2OCH3 phenyl 2-(aminosulfonyl)phenyl
    802 CH2OCH3 phenyl 2-(methylaminosulfonyl)phenyl
    803 CH2OCH3 phenyl 1-pyrrolidinocarbonyl
    804 CH2OCH3 phenyl 2-(methylsulfonyl)phenyl
    805 CH2OCH3 phenyl 4-morpholino
    806 CH2OCH3 phenyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    807 CH2OCH3 phenyl 4-morpholinocarbonyl
    808 CH2OCH3 phenyl 2-methyl-1-imidazolyl
    809 CH2OCH3 phenyl 5-methyl-1-imidazolyl
    810 CH2OCH3 phenyl 2-methylsulfonyl-1-imidazolyl
    811 CH2OCH3 2-pyridyl 2-(aminosulfonyl)phenyl
    812 CH2OCH3 2-pyridyl 2-(methylaminosulfonyl)phenyl
    813 CH2OCH3 2-pyridyl 1-pyrrolidinocarbonyl
    814 CH2OCH3 2-pyridyl 2-(methylsulfonyl)phenyl
    815 CH2OCH3 2-pyridyl 4-morpholino
    816 CH2OCH3 2-pyridyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    817 CH2OCH3 2-pyridyl 4-morpholinocarbonyl
    818 CH2OCH3 2-pyridyl 2-methyl-1-imidazolyl
    819 CH2OCH3 2-pyridyl 5-methyl-1-imidazolyl
    820 CH2OCH3 2-pyridyl 2-methylsulfonyl-1-imidazolyl
    821 CH2OCH3 3-pyridyl 2-(aminosulfonyl)phenyl
    822 CH2OCH3 3-pyridyl 2-(methylaminosulfonyl)phenyl
    823 CH2OCH3 3-pyridyl 1-pyrrolidinocarbonyl
    824 CH2OCH3 3-pyridyl 2-(methylsulfonyl)phenyl
    825 CH2OCH3 3-pyridyl 4-morpholino
    826 CH2OCH3 3-pyridyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    827 CH2OCH3 3-pyridyl 4-morpholinocarbonyl
    828 CH2OCH3 3-pyridyl 2-methyl-1-imidazolyl
    829 CH2OCH3 3-pyridyl 5-methyl-1-imidazolyl
    830 CH2OCH3 3-pyridyl 2-methylsulfonyl-1-imidazolyl
    831 CH2OCH3 2-pyrimidyl 2-(aminosulfonyl)phenyl
    832 CH2OCH3 2-pyrimidyl 2-(methylaminosulfonyl)phenyl
    833 CH2OCH3 2-pyrimidyl 1-pyrrolidinocarbonyl
    834 CH2OCH3 2-pyrimidyl 2-(methylsulfonyl)phenyl
    835 CH2OCH3 2-pyrimidyl 4-morpholino
    836 CH2OCH3 2-pyrimidyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    837 CH2OCH3 2-pyrimidyl 4-morpholinocarbonyl
    838 CH2OCH3 2-pyrimidyl 2-methyl-1-imidazolyl
    839 CH2OCH3 2-pyrimidyl 5-methyl-1-imidazolyl
    840 CH2OCH3 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl
    841 CH2OCH3 5-pyrimidyl 2-(aminosulfonyl)phenyl
    842 CH2OCH3 5-pyrimidyl 2-(methylaminosulfonyl)phenyl
    843 CH2OCH3 5-pyrimidyl 1-pyrrolidinocarbonyl
    844 CH2OCH3 5-pyrimidyl 2-(methylsulfonyl)phenyl
    845 CH2OCH3 5-pyrimidyl 4-morpholino
    846 CH2OCH3 5-pyrimidyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    847 CH2OCH3 5-pyrimidyl 4-morpholinocarbonyl
    848 CH2OCH3 5-pyrimidyl 2-methyl-1-imidazolyl
    849 CH2OCH3 5-pyrimidyl 5-methyl-1-imidazolyl
    850 CH2OCH3 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl
    851 CH2OCH3 2-Cl-phenyl 2-(aminosulfonyl)phenyl
    852 CH2OCH3 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl
    853 CH2OCH3 2-Cl-phenyl 1-pyrrolidinocarbonyl
    854 CH2OCH3 2-Cl-phenyl 2-(methylsulfonyl)phenyl
    855 CH2OCH3 2-Cl-phenyl 4-morpholino
    856 CH2OCH3 2-Cl-phenyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    857 CH2OCH3 2-Cl-phenyl 4-morpholinocarbonyl
    858 CH2OCH3 2-Cl-phenyl 2-methyl-1-imidazolyl
    859 CH2OCH3 2-Cl-phenyl 5-methyl-1-imidazolyl
    860 CH2OCH3 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl
    861 CH2OCH3 2-F-phenyl 2-(aminosulfonyl)phenyl
    862 CH2OCH3 2-F-phenyl 2-(methylaminosulfonyl)phenyl
    863 CH2OCH3 2-F-phenyl 1-pyrrolidinocarbonyl
    864 CH2OCH3 2-F-phenyl 2-(methylsulfonyl)phenyl
    865 CH2OCH3 2-F-phenyl 4-morpholino
    866 CH2OCH3 2-F-phenyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    867 CH2OCH3 2-F-phenyl 4-morpholinocarbonyl
    868 CH2OCH3 2-F-phenyl 2-methyl-1-imidazolyl
    869 CH2OCH3 2-F-phenyl 5-methyl-1-imidazolyl
    870 CH2OCH3 2-F-phenyl 2-methylsulfonyl-1-imidazolyl
    871 CH2OCH3 2,6-diF-phenyl 2-(aminosulfonyl)phenyl
    872 CH2OCH3 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl
    873 CH2OCH3 2,6-diF-phenyl 1-pyrrolidinocarbonyl
    874 CH2OCH3 2,6-diF-phenyl 2-(methylsulfonyl)phenyl
    875 CH2OCH3 2,6-diF-phenyl 4-morpholino
    876 CH2OCH3 2,6-diF-phenyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    877 CH2OCH3 2,6-diF-phenyl 4-morpholinocarbonyl
    878 CH2OCH3 2,6-diF-phenyl 2-methyl-1-imidazolyl
    879 CH2OCH3 2,6-diF-phenyl 5-methyl-1-imidazolyl
    880 CH2OCH3 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl
    881 CONH2 phenyl 2-(aminosulfonyl)phenyl
    882 CONH2 phenyl 2-(methylaminosulfonyl)phenyl
    883 CONH2 phenyl 1-pyrrolidinocarbonyl
    884 CONH2 phenyl 2-(methylsulfonyl)phenyl
    885 CONH2 phenyl 4-morpholino
    886 CONH2 phenyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    887 CONH2 phenyl 4-morpholinocarbonyl
    888 CONH2 phenyl 2-methyl-1-imidazolyl
    889 CONH2 phenyl 5-methyl-1-imidazolyl
    890 CONH2 phenyl 2-methylsulfonyl-1-imidazolyl
    891 CONH2 2-pyridyl 2-(aminosulfonyl)phenyl
    892 CONH2 2-pyridyl 2-(methylaminosulfonyl)phenyl
    893 CONH2 2-pyridyl 1-pyrrolidinocarbonyl
    894 CONH2 2-pyridyl 2-(methylsulfonyl)phenyl
    895 CONH2 2-pyridyl 4-morpholino
    896 CONH2 2-pyridyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    897 CONH2 2-pyridyl 4-morpholinocarbonyl
    898 CONH2 2-pyridyl 2-methyl-1-imidazolyl
    899 CONH2 2-pyridyl 5-methyl-1-imidazolyl
    900 CONH2 2-pyridyl 2-methylsulfonyl-1-imidazolyl
    901 CONH2 3-pyridyl 2-(aminosulfonyl)phenyl
    902 CONH2 3-pyridyl 2-(methylaminosulfonyl)phenyl
    903 CONH2 3-pyridyl 1-pyrrolidinocarbonyl
    904 CONH2 3-pyridyl 2-(methylsulfonyl)phenyl
    905 CONH2 3-pyridyl 4-morpholino
    906 CONH2 3-pyridyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    907 CONH2 3-pyridyl 4-morpholinocarbonyl
    908 CONH2 3-pyridyl 2-methyl-1-imidazolyl
    909 CONH2 3-pyridyl 5-methyl-1-imidazolyl
    910 CONH2 3-pyridyl 2-methylsulfonyl-1-imidazolyl
    911 CONH2 2-pyrimidyl 2-(aminosulfonyl)phenyl
    912 CONH2 2-pyrimidyl 2-(methylaminosulfonyl)phenyl
    913 CONH2 2-pyrimidyl 1-pyrrolidinocarbonyl
    914 CONH2 2-pyrimidyl 2-(methylsulfonyl)phenyl
    915 CONH2 2-pyrimidyl 4-morpholino
    916 CONH2 2-pyrimidyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    917 CONH2 2-pyrimidyl 4-morpholinocarbonyl
    918 CONH2 2-pyrimidyl 2-methyl-1-imidazolyl
    919 CONH2 2-pyrimidyl 5-methyl-1-imidazolyl
    920 CONH2 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl
    921 CONH2 5-pyrimidyl 2-(aminosulfonyl)phenyl
    922 CONH2 5-pyrimidyl 2-(methylaminosulfonyl)phenyl
    923 CONH2 5-pyrimidyl 1-pyrrolidinocarbonyl
    924 CONH2 5-pyrimidyl 2-(methylsulfonyl)phenyl
    925 CONH2 5-pyrimidyl 4-morpholino
    926 CONH2 5-pyrimidyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    927 CONH2 5-pyrimidyl 4-morpholinocarbonyl
    928 CONH2 5-pyrimidyl 2-methyl-1-imidazolyl
    929 CONH2 5-pyrimidyl 5-methyl-1-imidazolyl
    930 CONH2 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl
    931 CONH2 2-Cl-phenyl 2-(aminosulfonyl)phenyl
    932 CONH2 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl
    933 CONH2 2-Cl-phenyl 1-pyrrolidinocarbonyl
    934 CONH2 2-Cl-phenyl 2-(methylsulfonyl)phenyl
    935 CONH2 2-Cl-phenyl 4-morpholino
    936 CONH2 2-Cl-phenyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    937 CONH2 2-Cl-phenyl 4-morpholinocarbonyl
    938 CONH2 2-Cl-phenyl 2-methyl-1-imidazolyl
    939 CONH2 2-Cl-phenyl 5-methyl-1-imidazolyl
    940 CONH2 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl
    941 CONH2 2-F-phenyl 2-(aminosulfonyl)phenyl
    942 CONH2 2-F-phenyl 2-(methylaminosulfonyl)phenyl
    943 CONH2 2-F-phenyl 1-pyrrolidinocarbonyl
    944 CONH2 2-F-phenyl 2-(methylsulfonyl)phenyl
    945 CONH2 2-F-phenyl 4-morpholino
    946 CONH2 2-F-phenyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    947 CONH2 2-F-phenyl 4-morpholinocarbonyl
    948 CONH2 2-F-phenyl 2-methyl-1-imidazolyl
    949 CONH2 2-F-phenyl 5-methyl-1-imidazolyl
    950 CONH2 2-F-phenyl 2-methylsulfonyl-1-imidazolyl
    951 CONH2 2,6-diF-phenyl 2-(aminosulfonyl)phenyl
    952 CONH2 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl
    953 CONH2 2,6-diF-phenyl 1-pyrrolidinocarbonyl
    954 CONH2 2,6-diF-phenyl 2-(methylsulfonyl)phenyl
    955 CONH2 2,6-diF-phenyl 4-morpholino
    956 CONH2 2,6-diF-phenyl 2-(1′-CF3-tetrazol-2-
    yl)phenyl
    957 CONH2 2,6-diF-phenyl 4-morpholinocarbonyl
    958 CONH2 2,6-diF-phenyl 2-methyl-1-imidazolyl
    959 CONH2 2,6-diF-phenyl 5-methyl-1-imidazolyl
    960 CONH2 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl
  • 247.
    TABLE 2
  • 248.
    Ex # A B
    1 phenyl 2-(aminosulfonyl)phenyl
    2 phenyl 2-(methylaminosulfonyl)phenyl
    3 phenyl 1-pyrrolidinocarbonyl
    4 phenyl 2-(methylsulfonyl)phenyl
    5 phenyl 4-morpholino
    6 phenyl 2-(1′-CF3-tetrazol-2-yl)phenyl
    7 phenyl 4-morpholinocarbonyl
    8 phenyl 2-methyl-1-imidazolyl
    9 phenyl 5-methyl-1-imidazolyl
    10 phenyl 2-methylsulfonyl-1-imidazolyl
    11 2-pyridyl 2-(aminosulfonyl)phenyl
    12 2-pyridyl 2-(methylaminosulfonyl)phenyl
    13 2-pyridyl 1-pyrrolidinocarbonyl
    14 2-pyridyl 2-(methylsulfonyl)phenyl
    15 2-pyridyl 4-morpholino
    16 2-pyridyl 2-(1′-CF3-tetrazol-2-yl)phenyl
    17 2-pyridyl 4-morpholinocarbonyl
    18 2-pyridyl 2-methyl-1-imidazolyl
    19 2-pyridyl 5-methyl-1-imidazolyl
    20 2-pyridyl 2-methylsulfonyl-1-imidazolyl
    21 3-pyridyl 2-(aminosulfonyl)phenyl
    22 3-pyridyl 2-(methylaminosulfonyl)phenyl
    23 3-pyridyl 1-pyrrolidinocarbonyl
    24 3-pyridyl 2-(methylsulfonyl)phenyl
    25 3-pyridyl 4-morpholino
    26 3-pyridyl 2-(1′-CF3-tetrazol-2-yl)phenyl
    27 3-pyridyl 4-morpholinocarbonyl
    28 3-pyridyl 2-methyl-1-imidazolyl
    29 3-pyridyl 5-methyl-1-imidazolyl
    30 3-pyridyl 2-methylsulfonyl-1-imidazolyl
    31 2-pyrimidyl 2-(aminosulfonyl)phenyl
    32 2-pyrimidyl 2-(methylaminosulfonyl)phenyl
    33 2-pyrimidyl 1-pyrrolidinocarbonyl
    34 2-pyrimidyl 2-(methylsulfonyl)phenyl
    35 2-pyrimidyl 4-morpholino
    36 2-pyrimidyl 2-(1′-CF3-tetrazol-2-yl)phenyl
    37 2-pyrimidyl 4-morpholinocarbonyl
    38 2-pyrimidyl 2-methyl-1-imidazolyl
    39 2-pyrimidyl 5-methyl-1-imidazolyl
    40 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl
    41 5-pyrimidyl 2-(aminosulfonyl)phenyl
    42 5-pyrimidyl 2-(methylaminosulfonyl)phenyl
    43 5-pyrimidyl 1-pyrrolidinocarbonyl
    44 5-pyrimidyl 2-(methylsulfonyl)phenyl
    45 5-pyrimidyl 4-morpholino
    46 5-pyrimidyl 2-(1′-CF3-tetrazol-2-yl)phenyl
    47 5-pyrimidyl 4-morpholinocarbonyl
    48 5-pyrimidyl 2-methyl-1-imidazolyl
    49 5-pyrimidyl 5-methyl-1-imidazolyl
    50 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl
    51 2-Cl-phenyl 2-(aminosulfonyl)phenyl
    52 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl
    53 2-Cl-phenyl 1-pyrrolidinocarbonyl
    54 2-Cl-phenyl 2-(methylsulfonyl)phenyl
    55 2-Cl-phenyl 4-morpholino
    56 2-Cl-phenyl 2-(1′-CF3-tetrazol-2-yl)phenyl
    57 2-Cl-phenyl 4-morpholinocarbonyl
    58 2-Cl-phenyl 2-methyl-1-imidazolyl
    59 2-Cl-phenyl 5-methyl-1-imidazolyl
    60 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl
    61 2-F-phenyl 2-(aminosulfonyl)phenyl
    62 2-F-phenyl 2-(methylaminosulfonyl)phenyl
    63 2-F-phenyl 1-pyrrolidinocarbonyl
    64 2-F-phenyl 2-(methylsulfonyl)phenyl
    65 2-F-phenyl 4-morpholino
    66 2-F-phenyl 2-(1′-CF3-tetrazol-2-yl)phenyl
    67 2-F-phenyl 4-morpholinocarbonyl
    68 2-F-phenyl 2-methyl-1-imidazolyl
    69 2-F-phenyl 5-methyl-1-imidazolyl
    70 2-F-phenyl 2-methylsulfonyl-1-imidazolyl
    71 2,6-diF-phenyl 2-(aminosulfonyl)phenyl
    72 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl
    73 2,6-diF-phenyl 1-pyrrolidinocarbonyl
    74 2,6-diF-phenyl 2-(methylsulfonyl)phenyl
    75 2,6-diF-phenyl 4-morpholino
    76 2,6-diF-phenyl 2-(1′-CF3-tetrazol-2-yl)phenyl
    77 2,6-diF-phenyl 4-morpholinocarbonyl
    78 2,6-diF-phenyl 2-methyl-1-imidazolyl
    79 2,6-diF-phenyl 5-methyl-1-imidazolyl
    80 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl
    • Utility
  • 249. The compounds of this invention are useful as anticoagulants for the treatment or prevention of thromboembolic disorders in mammals. The term “thromboembolic disorders” as used herein includes arterial or venous cardiovascular or cerebrovascular thromboembolic disorders, including, for example, unstable angina, first or recurrent myocardial infarction, ischemic sudden death, transient ischemic attack, stroke, atherosclerosis, venous thrombosis, deep vein thrombosis, thrombophlebitis, arterial embolism, coronary and cerebral arterial thrombosis, cerebral embolism, kidney embolisms, and pulmonary embolisms. The anticoagulant effect of compounds of the present invention is believed to be due to inhibition of factor Xa or thrombin.
  • 250. The effectiveness of compounds of the present invention as inhibitors of factor Xa was determined using purified human factor Xa and synthetic substrate. The rate of factor Xa hydrolysis of chromogenic substrate S2222 (Kabi Pharmacia, Franklin, Ohio) was measured both in the absence and presence of compounds of the present invention. Hydrolysis of the substrate resulted in the release of pNA, which was monitored spectrophotometrically by measuring the increase in absorbance at 405 nM. A decrease in the rate of absorbance change at 405 nm in the presence of inhibitor is indicative of enzyme inhibition. The results of this assay are expressed as inhibitory constant, Ki.
  • 251. Factor Xa determinations were made in 0.10 M sodium phosphate buffer, pH 7.5, containing 0.20 M NaCl, and 0.5% PEG 8000. The Michaelis constant, Km, for substrate hydrolysis was determined at 25° C. using the method of Lineweaver and Burk. Values of Ki were determined by allowing 0.2-0.5 nM human factor Xa (Enzyme Research Laboratories, South Bend, Ind.) to react with the substrate (0.20 mM-1 mM) in the presence of inhibitor. Reactions were allowed to go for 30 minutes and the velocities (rate of absorbance change vs time) were measured in the time frame of 25-30 minutes. The following relationship was used to calculate Ki values:
  • 252.
    Figure US20010000179A1-20010405-C00026
  • 253. where:
  • 254. vo is the velocity of the control in the absence of inhibitor;
  • 255. vs is the velocity in the presence of inhibitor;
  • 256. I is the concentration of inhibitor;
  • 257. Ki is the dissociation constant of the enzyme:inhibitor complex;
  • 258. S is the concentration of substrate;
  • 259. Km is the Michaelis constant.
  • 260. Using the methodology described above, a compound of the present invention were found to exhibit a Ki of <10 μM, thereby confirming the utility of the compounds of the present invention as effective Xa inhibitors.
  • 261. The antithrombotic effect of compounds of the present invention can be demonstrated in a rabbit arterio-venous (AV) shunt thrombosis model. In this model, rabbits weighing 2-3 kg anesthetized with a mixture of xylazine (10 mg/kg i.m.) and ketamine (50 mg/kg i.m.) are used. A saline-filled AV shunt device is connected between the femoral arterial and the femoral venous cannulae. The AV shunt device consists of a piece of 6-cm tygon tubing which contains a piece of silk thread. Blood will flow from the femoral artery via the AV-shunt into the femoral vein. The exposure of flowing blood to a silk thread will induce the formation of a significant thrombus. After forty minutes, the shunt is disconnected and the silk thread covered with thrombus is weighed. Test agents or vehicle will be given (i.v., i.p., s.c., or orally) prior to the opening of the AV shunt. The percentage inhibition of thrombus formation is determined for each treatment group. The ID50 values (dose which produces 50% inhibition of thrombus formation) are estimated by linear regression.
  • 262. The compounds of formula (I) may also be useful as inhibitors of serine proteases, notably human thrombin, plasma kallikrein and plasmin. Because of their inhibitory action, these compounds are indicated for use in the prevention or treatment of physiological reactions, blood coagulation and inflammation, catalyzed by the aforesaid class of enzymes. Specifically, the compounds have utility as drugs for the treatment of diseases arising from elevated thrombin activity such as myocardial infarction, and as reagents used as anticoagulants in the processing of blood to plasma for diagnostic and other commercial purposes.
  • 263. Some compounds of the present invention were shown to be direct acting inhibitors of the serine protease thrombin by their ability to inhibit the cleavage of small molecule substrates by thrombin in a purified system. In vitro inhibition constants were determined by the method described by Kettner et al. in J. Biol. Chem. 265, 18289-18297 (1990), herein incorporated by reference. In these assays, thrombin-mediated hydrolysis of the chromogenic substrate S2238 (Helena Laboratories, Beaumont, Tx.) was monitored spectrophotometrically. Addition of an inhibitor to the assay mixture results in decreased absorbance and is indicative of thrombin inhibition. Human thrombin (Enzyme Research Laboratories, Inc., South Bend, Ind.) at a concentration of 0.2 nM in 0.10 M sodium phosphate buffer, pH 7.5, 0.20 M NaCl, and 0.5% PEG 6000, was incubated with various substrate concentrations ranging from 0.20 to 0.02 mM. After 25 to 30 minutes of incubation, thrombin activity was assayed by monitoring the rate of increase in absorbance at 405 nm which arises owing to substrate hydrolysis. Inhibition constants were derived from reciprocal plots of the reaction velocity as a function of substrate concentration using the standard method of Lineweaver and Burk. Using the methodology described above, some compounds of this invention were evaluated and found to exhibit a Ki of less than 10 μm, thereby confirming the utility of the compounds of the present invention as effective thrombin inhibitors.
  • 264. The compounds of the present invention can be administered alone or in combination with one or more additional therapeutic agents. These include other anti-coagulant or coagulation inhibitory agents, anti-platelet or platelet inhibitory agents, thrombin inhibitors, or thrombolytic or fibrinolytic agents.
  • 265. The compounds are administered to a mammal in a therapeutically effective amount. By “therapeutically effective amount” it is meant an amount of a compound of Formula I that, when administered alone or in combination with an additional therapeutic agent to a mammal, is effective to prevent or ameliorate the thromboembolic disease condition or the progression of the disease.
  • 266. By “administered in combination” or “combination therapy” it is meant that the compound of Formula I and one or more additional therapeutic agents are administered concurrently to the mammal being treated. When administered in combination each component may be administered at the same time or sequentially in any order at different points in time. Thus, each component may be administered separately but sufficiently closely in time so as to provide the desired therapeutic effect. Other anticoagulant agents (or coagulation inhibitory agents) that may be used in combination with the compounds of this invention include warfarin and heparin, as well as other factor Xa inhibitors such as those described in the publications identified above under Background of the Invention.
  • 267. The term anti-platelet agents (or platelet inhibitory agents), as used herein, denotes agents that inhibit platelet function such as by inhibiting the aggregation, adhesion or granular secretion of platelets. Such agents include, but are not limited to, the various known non-steroidal anti-inflammatory drugs (NSAIDS) such as aspirin, ibuprofen, naproxen, sulindac, indomethacin, mefenamate, droxicam, diclofenac, sulfinpyrazone, and piroxicam, including pharmaceutically acceptable salts or prodrugs thereof. Of the NSAIDS, aspirin (acetylsalicyclic acid or ASA), and piroxicam are preferred. Other suitable anti-platelet agents include ticlopidine, including pharmaceutically acceptable salts or prodrugs thereof. Ticlopidine is also a preferred compound since it is known to be gentle on the gastro-intestinal tract in use. Still other suitable platelet inhibitory agents include IIb/IIIa antagonists, thromboxane-A2-receptor antagonists and thromboxane-A2-synthetase inhibitors, as well as pharmaceutically acceptable salts or prodrugs thereof.
  • 268. The term thrombin inhibitors (or anti-thrombin agents), as used herein, denotes inhibitors of the serine protease thrombin. By inhibiting thrombin, various thrombin-mediated processes, such as thrombin-mediated platelet activation (that is, for example, the aggregation of platelets, and/or the granular secretion of plasminogen activator inhibitor-1 and/or serotonin) and/or fibrin formation are disrupted. A number of thrombin inhibitors are known to one of skill in the art and these inhibitors are contemplated to be used in combination with the present compounds. Such inhibitors include, but are not limited to, boroarginine derivatives, boropeptides, heparins, hirudin and argatroban, including pharmaceutically acceptable salts and prodrugs thereof. Boroarginine derivatives and boropeptides include N-acetyl and peptide derivatives of boronic acid, such as C-terminal a-aminoboronic acid derivatives of lysine, ornithine, arginine, homoarginine and corresponding isothiouronium analogs thereof. The term hirudin, as used herein, includes suitable derivatives or analogs of hirudin, referred to herein as hirulogs, such as disulfatohirudin. Boropeptide thrombin inhibitors include compounds described in Kettner et al., U.S. Pat. No. 5,187,157 and European Patent Application Publication Number 293 881 A2, the disclosures of which are hereby incorporated herein by reference. Other suitable boroarginine derivatives and boropeptide thrombin inhibitors include those disclosed in PCT Application Publication Number 92/07869 and European Patent Application Publication Number 471,651 A2, the disclosures of which are hereby incorporated herein by reference.
  • 269. The term thrombolytics (or fibrinolytic) agents (or thrombolytics or fibrinolytics), as used herein, denotes agents that lyse blood clots (thrombi). Such agents include tissue plasminogen activator, anistreplase, urokinase or streptokinase, including pharmaceutically acceptable salts or prodrugs thereof. The term anistreplase, as used herein, refers to anisoylated plasminogen streptokinase activator complex, as described, for example, in European Patent Application No. 028,489, the disclosure of which is hereby incorporated herein by reference herein. The term urokinase, as used herein, is intended to denote both dual and single chain urokinase, the latter also being referred to herein as prourokinase.
  • 270. Administration of the compounds of Formula I of the invention in combination with such additional therapeutic agent, may afford an efficacy advantage over the compounds and agents alone, and may do so while permitting the use of lower doses of each. A lower dosage minimizes the potential of side effects, thereby providing an increased margin of safety.
  • 271. The compounds of the present invention are also useful as standard or reference compounds, for example as a quality standard or control, in tests or assays involving the inhibition of factor Xa. Such compounds may be provided in a commercial kit, for example, for use in pharmaceutical research involving factor Xa. For example, a compound of the present invention could be used as a reference in an assay to compare its known activity to a compound with an unknown activity. This would ensure the experimenter that the assay was being performed properly and provide a basis for comparison, especially if the test compound was a derivative of the reference compound. When developing new assays or protocols, compounds according to the present invention could be used to test their effectiveness.
  • 272. The compounds of the present invention may also be used in diagnostic assays involving factor Xa. For example, the presence of factor Xa in an unknown sample could be determined by addition of chromogenic substrate S2222 to a series of solutions containing test sample and optionally one of the compounds of the present invention. If production of pNA is observed in the solutions containing test sample, but not in the presence of a compound of the present invention, then one would conclude factor Xa was present.
    • Dosage and Formulation
  • 273. The compounds of this invention can be administered in such oral dosage forms as tablets, capsules (each of which includes sustained release or timed release formulations), pills, powders, granules, elixirs, tinctures, suspensions, syrups, and emulsions. They may also be administered in intravenous (bolus or infusion), intraperitoneal, subcutaneous, or intramuscular form, all using dosage forms well known to those of ordinary skill in the pharmaceutical arts. They can be administered alone, but generally will be administered with a pharmaceutical carrier selected on the basis of the chosen route of administration and standard pharmaceutical practice.
  • 274. The dosage regimen for the compounds of the present invention will, of course, vary depending upon known factors, such as the pharmacodynamic characteristics of the particular agent and its mode and route of administration; the species, age, sex, health, medical condition, and weight of the recipient; the nature and extent of the symptoms; the kind of concurrent treatment; the frequency of treatment; the route of administration, the renal and hepatic function of the patient, and the effect desired. A physician or veterinarian can determine and prescribe the effective amount of the drug required to prevent, counter, or arrest the progress of the thromboembolic disorder.
  • 275. By way of general guidance, the daily oral dosage of each active ingredient, when used for the indicated effects, will range between about 0.001 to 1000 mg/kg of body weight, preferably between about 0.01 to 100 mg/kg of body weight per day, and most preferably between about 1.0 to 20 mg/kg/day. Intravenously, the most preferred doses will range from about 1 to about 10 mg/kg/minute during a constant rate infusion. Compounds of this invention may be administered in a single daily dose, or the total daily dosage may be administered in divided doses of two, three, or four times daily.
  • 276. Compounds of this invention can be administered in intranasal form via topical use of suitable intranasal vehicles, or via transdermal routes, using transdermal skin patches. When administered in the form of a transdermal delivery system, the dosage administration will, of course, be continuous rather than intermittent throughout the dosage regimen.
  • 277. The compounds are typically administered in admixture with suitable pharmaceutical diluents, excipients, or carriers (collectively referred to herein as pharmaceutical carriers) suitably selected with respect to the intended form of administration, that is, oral tablets, capsules, elixirs, syrups and the like, and consistent with conventional pharmaceutical practices.
  • 278. For instance, for oral administration in the form of a tablet or capsule, the active drug component can be combined with an oral, non-toxic, pharmaceutically acceptable, inert carrier such as lactose, starch, sucrose, glucose, methyl callulose, magnesium stearate, dicalcium phosphate, calcium sulfate, mannitol, sorbitol and the like; for oral administration in liquid form, the oral drug components can be combined with any oral, non-toxic, pharmaceutically acceptable inert carrier such as ethanol, glycerol, water, and the like. Moreover, when desired or necessary, suitable binders, lubricants, disintegrating agents, and coloring agents can also be incorporated into the mixture. Suitable binders include starch, gelatin, natural sugars such as glucose or beta-lactose, corn sweeteners, natural and synthetic gums such as acacia, tragacanth, or sodium alginate, carboxymethylcellulose, polyethylene glycol, waxes, and the like. Lubricants used in these dosage forms include sodium oleate, sodium stearate, magnesium stearate, sodium benzoate, sodium acetate, sodium chloride, and the like. Disintegrators include, without limitation, starch, methyl cellulose, agar, bentonite, xanthan gum, and the like.
  • 279. The compounds of the present invention can also be administered in the form of liposome delivery systems, such as small unilamellar vesicles, large unilamellar vesicles, and multilamellar vesicles. Liposomes can be formed from a variety of phospholipids, such as cholesterol, stearylamine, or phosphatidylcholines.
  • 280. Compounds of the present invention may also be coupled with soluble polymers as targetable drug carriers. Such polymers can include polyvinylpyrrolidone, pyran copolymer, polyhydroxypropylmethacrylamide-phenol, polyhydroxyethylaspartamidephenol, or polyethyleneoxide-polylysine substituted with palmitoyl residues. Furthermore, the compounds of the present invention may be coupled to a class of biodegradable polymers useful in achieving controlled release of a drug, for example, polylactic acid, polyglycolic acid, copolymers of polylactic and polyglycolic acid, polyepsilon caprolactone, polyhydroxy butyric acid, polyorthoesters, polyacetals, polydihydropyrans, polycyanoacylates, and crosslinked or amphipathic block copolymers of hydrogels.
  • 281. Dosage forms (pharmaceutical compositions) suitable for administration may contain from about 1 milligram to about 100 milligrams of active ingredient per dosage unit. In these pharmaceutical compositions the active ingredient will ordinarily be present in an amount of about 0.5-95% by weight based on the total weight of the composition.
  • 282. Gelatin capsules may contain the active ingredient and powdered carriers, such as lactose, starch, cellulose derivatives, magnesium stearate, stearic acid, and the like. Similar diluents can be used to make compressed tablets. Both tablets and capsules can be manufactured as sustained release products to provide for continuous release of medication over a period of hours. Compressed tablets can be sugar coated or film coated to mask any unpleasant taste and protect the tablet from the atmosphere, or enteric coated for selective disintegration in the gastrointestinal tract.
  • 283. Liquid dosage forms for oral administration can contain coloring and flavoring to increase patient acceptance.
  • 284. In general, water, a suitable oil, saline, aqueous dextrose (glucose), and related sugar solutions and glycols such as propylene glycol or polyethylene glycols are suitable carriers for parenteral solutions. Solutions for parenteral administration preferably contain a water soluble salt of the active ingredient, suitable stabilizing agents, and if necessary, buffer substances. Antioxidizing agents such as sodium bisulfite, sodium sulfite, or ascorbic acid, either alone or combined, are suitable stabilizing agents. Also used are citric acid and its salts and sodium EDTA. In addition, parenteral solutions can contain preservatives, such as benzalkonium chloride, methyl- or propyl-paraben, and chlorobutanol.
  • 285. Suitable pharmaceutical carriers are described in Remington's Pharmaceutical Sciences, Mack Publishing Company, a standard reference text in this field.
  • 286. Representative useful pharmaceutical dosage-forms for administration of the compounds of this invention can be illustrated as follows:
  • 287. Capsules
  • 288. A large number of unit capsules can be prepared by filling standard two-piece hard gelatin capsules each with 100 milligrams of powdered active ingredient, 150 milligrams of lactose, 50 milligrams of cellulose, and 6 milligrams magnesium stearate.
  • 289. Soft Gelatin Capsules
  • 290. A mixture of active ingredient in a digestable oil such as soybean oil, cottonseed oil or olive oil may be prepared and injected by means of a positive displacement pump into gelatin to form soft gelatin capsules containing 100 milligrams of the active ingredient. The capsules should be washed and dried.
  • 291. Tablets
  • 292. Tablets may be prepared by conventional procedures so that the dosage unit is 100 milligrams of active ingredient, 0.2 milligrams of colloidal silicon dioxide, 5 milligrams of magnesium stearate, 275 milligrams of microcrystalline cellulose, 11 milligrams of starch and 98.8 milligrams of lactose. Appropriate coatings may be applied to increase palatability or delay absorption.
  • 293. Injectable
  • 294. A parenteral composition suitable for administration by injection may be prepared by stirring 1.5% by weight of active ingredient in 10% by volume propylene glycol and water. The solution should be made isotonic with sodium chloride and sterilized.
  • 295. Suspension
  • 296. An aqueous suspension can be prepared for oral administration so that each 5 mL contain 100 mg of finely divided active ingredient, 200 mg of sodium carboxymethyl cellulose, 5 mg of sodium benzoate, 1.0 g of sorbitol solution, U.S.P., and 0.025 mL of vanillin.
  • 297. Where the compounds of this invention are combined with other anticoagulant agents, for example, a daily dosage may be about 0.1 to 100 milligrams of the compound of Formula I and about 1 to 7.5 milligrams of the second anticoagulant, per kilogram of patient body weight. For a tablet dosage form, the compounds of this invention generally may be present in an amount of about 5 to 10 milligrams per dosage unit, and the second anti-coagulant in an amount of about 1 to 5 milligrams per dosage unit.
  • 298. Where the compounds of Formula I are administered in combination with an anti-platelet agent, by way of general guidance, typically a daily dosage may be about 0.01 to 25 milligrams of the compound of Formula I and about 50 to 150 milligrams of the anti-platelet agent, preferably about 0.1 to 1 milligrams of the compound of Formula I and about 1 to 3 milligrams of antiplatelet agents, per kilogram of patient body weight.
  • 299. Where the compounds of Formula I are adminstered in combination with thrombolytic agent, typically a daily dosage may be about 0.1 to 1 milligrams of the compound of Formula I, per kilogram of patient body weight and, in the case of the thrombolytic agents, the usual dosage of the thrombolyic agent when administered alone may be reduced by about 70-80% when administered with a compound of Formula I.
  • 300. Where two or more of the foregoing second therapeutic agents are administered with the compound of Formula I, generally the amount of each component in a typical daily dosage and typical dosage form may be reduced relative to the usual dosage of the agent when administered alone, in view of the additive or synergistic effect of the therapeutic agents when administered in combination.
  • 301. Particularly when provided as a single dosage unit, the potential exists for a chemical interaction between the combined active ingredients. For this reason, when the compound of Formula I and a second therapeutic agent are combined in a single dosage unit they are formulated such that although the active ingredients are combined in a single dosage unit, the physical contact between the active ingredients is minimized (that is, reduced). For example, one active ingredient may be enteric coated. By enteric coating one of the active ingredients, it is possible not only to minimize the contact between the combined active ingredients, but also, it is possible to control the release of one of these components in the gastrointestinal tract such that one of these components is not released in the stomach but rather is released in the intestines. One of the active ingredients may also be coated with a material which effects a sustained-release throughout the gastrointestinal tract and also serves to minimize physical contact between the combined active ingredients. Furthermore, the sustained-released component can be additionally enteric coated such that the release of this component occurs only in the intestine. Still another approach would involve the formulation of a combination product in which the one component is coated with a sustained and/or enteric release polymer, and the other component is also coated with a polymer such as a low-viscosity grade of hydroxypropyl methylcellulose (HPMC) or other appropriate materials as known in the art, in order to further separate the active components. The polymer coating serves to form an additional barrier to interaction with the other component.
  • 302. These as well as other ways of minimizing contact between the components of combination products of the present invention, whether administered in a single dosage form or administered in separate forms but at the same time by the same manner, will be readily apparent to those skilled in the art, once armed with the present disclosure.
  • 303. Obviously, numerous modifications and variations of the present invention are possible in light of the above teachings. It is therefore to be understood that within the scope of the appended claims, the invention may be practiced otherwise that as specific

Claims (17)

ally described herein. What is claimed is:
1. A compound of formula I:
Figure US20010000179A1-20010405-C00027
or a stereoisomer or pharmaceutically acceptable salt thereof, wherein;
M1 is N or CR1c;
M2 is NR1a or CR1aR1a, provided that only one of M1 and M2 is a N atom;
D is selected from C(═NR8)NR7R9, NHC(═NR8)NR7R9, NR8CH(═NR7), C(O)NR7R8, and CR8R9NR7R8;
E is selected from phenyl, pyridyl, pyrimidyl, pyrazinyl, pyridazinyl, and piperidinyl substituted with 1 R;
alternatively, D—E—G together represent pyridyl substituted with 1 R;
R is selected from H, Cl, F, Br, I, (CH2)tOR3, C1-4 alkyl, OCF3, CF3, C(O)NR7R8, and (CR8R9)tNR7R8;
G is selected from NHCH2, OCH2, and SCH2, provided that when s is 0, then G is absent;
Z is selected from a C1-4 alkylene, (CH2)rO(CH2)r, (CH2)rNR3(CH2)r, (CH2)rC(O)(CH2)r, (CH2)rC(O)O(CH2)r, (CH2)rOC(O)(CH2)r, (CH2)rC(O)NR3(CH2)r, (CH2)rNR3C(O)(CH2)r, (CH2)rOC(O)O(CH2)r, (CH2)rOC(O)NR3(CH2)r, (CH2)rNR3C(O)O(CH2)r, (CH2)rNR3C(O)NR3(CH2)r, (CH2)rS(O)p(CH2)r, (CH2)rSO2NR3(CH2)r, (CH2)rNR3SO2(CH2)r, and (CH2)rNR3SO2NR3(CH2)r, provided that Z does not form a N—N, N—O, N—S, NCH2N, NCH2O, or NCH2S bond with group A;
R1a and R1b are, at each occurrence, independently selected from H, —(CH2)r—R1′, NCH2R1″, OCH2R1″, SCH2R1″, N(CH2)2(CH2)tR1′, O(CH2)2(CH2)tR1′, and S(CH2)2(CH2)tR1′;
R1c is selected from H, —(CH2)q—R1′, C1-3 alkyl, C(O)R2c, (CF2)rCO2R2c, C(O)NR2R2a, C3-6 carbocyclic residue substituted with 0-2 R4, and 5-10 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-2 R4;
R1′ is selected from H, C1-3 alkyl, halo, (CF2)rCF3, OR2, NR2R2a, C(O)R2c, OC(O)R2, (CF2)rCO2R2c, S(O)pR2b, NR2(CH2)rOR2, NR2C(O)R2b, NR2C(O)NHR2b, NR2C(O)2R2a, OC(O)NR2b, C(O)NR2R2a, SO2NR2R2a, NR2SO2R2b, C3-6 carbocyclic residue substituted with 0-2 R4, and 5-10 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-2 R4;
R1″ is selected from H, C(O)R2b, C(O)NR2R2a, S(O)R2b, S(O)2R2b, and SO2NR2R2a;
R2, at each occurrence, is selected from H, CF3, C1-6 alkyl, benzyl, C3-6 carbocyclic residue substituted with 0-2 R4b, and 5-6 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-2 R4b;
R2a, at each occurrence, is selected from H, CF3, C1-6 alkyl, benzyl, C3-6 carbocyclic residue substituted with 0-2 R4b, and 5-6 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-2 R4b;
R2b, at each occurrence, is selected from CF3, C1-4 alkoxy, C1-6 alkyl, benzyl, C3-6 carbocyclic residue substituted with 0-2 R4b, and 5-6 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-2 R4b;
R2c, at each occurrence, is selected from CF3, OH, C1-4 alkoxy, C1-6 alkyl, benzyl, C3-6 carbocyclic residue substituted with 0-2 R4b, and 5-6 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-2 R4b;
alternatively, R2 and R2a combine to form a 5 or 6 membered saturated, partially saturated or unsaturated ring substituted with 0-2 R4b which contains from 0-1 additional heteroatoms selected from the group consisting of N, O, and S;
R3, at each occurrence, is selected from H, C1-4 alkyl, and phenyl;
R3a, at each occurrence, is selected from H, C1-4 alkyl, and phenyl;
A is selected from:
C3-10 carbocyclic residue substituted with 0-2 R4, and
5-10 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-2 R4;
B is selected from:
X—Y, NR2R2a, C(═NR2)NR2R2a, NR2C(═NR2)NR2R2a,
C3-10 carbocyclic residue substituted with 0-2 R4a, and
5-10 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-2 R4a;
X is selected from C1-4 alkylene, —CR2(CR2R2b)(CH2)t—, —C(O)—, —C(═NR)—, —CR2(NR1″R2)—, —CR2(OR2)—, —CR2(SR2)—, —C(O)CR2R2a—, —CR2R2aC(O), —S(O)p—, —S(O)pCR2R2a—, —CR2R2aS(O)p—, —S(O)2NR2—, —NR2S(O)2—, —NR2S(O)2CR2R2a—, —CR2R2aS(O)2NR2—, —NR2S(O)2NR2—, —C(O)NR2—, —NR2C(O)—, —C(O)NR2CR2R2a—, —NR2C(O)CR2R2a—, —CR2R2aC(O)NR2—, —CR2R2aNR2C(O)—, —NR2C(O)O—, —OC(O)NR2—, —NR2C(O)NR2—, —NR2—, NR2CR2R2a—, —CR2R2aNR2—, O, —CR2R2aO—, and —OCR2R2a—;
Y is selected from:
(CH2)rNR2R2a, provided that X—Y do not form a N—N, O—N, or S—N bond,
C3-10 carbocyclic residue substituted with 0-2 R4a, and
5-10 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-2 R4a;
R4, at each occurrence, is selected from ═O, (CH2)rOR2, halo, C1-4 alkyl, —CN, NO2, (CH2)rNR2R2a, (CH2)rC(O)R2b, NR2C(O)R2b, C(O)NR2R2a, NR2C(O)NR2R2a, CH(═NR2)NR2R2a, NHC(═NR2)NR2R2a, SO2NR2R2a, NR2SO2NR2R2a, NR2SO2-C1-4 alkyl, NR2SO2R5, S(O)pR5, (CF2)rCF3, NCH2R1″, OCH2R1″, SCH2R1″, N(CH2)2(CH2)tR1′, O(CH2)2(CH2)tR1′, and S(CH2)2(CH2)tR1′,
alternatively, one R4 is a 5-6 membered aromatic heterocycle containing from 1-4 heteroatoms selected from the group consisting of N, O, and S;
R4a, at each occurrence, is selected from ═O, (CH2)rOR2, halo, C1-4 alkyl, —CN, NO2, (CH2)rNR2R2a, (CH2)rC(O)R2b, NR2C(O)R2b, C(O)NR2R2a, NR2C(O)NR2R2a, CH(═NR2)NR2R2a, NHC(═NR2)NR2R2a, SO2NR2R2a, NR2SO2NR2R2a, NR2SO2-C1-4 alkyl, NR2SO2R5, S(O)pR5, and (CF2)rCF3;
alternatively, one R4a is a 5-6 membered aromatic heterocycle containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-1 R5;
R4b, at each occurrence, is selected from ═O, (CH2)rOR3, halo, C1-4 alkyl, —CN, NO2, (CH2)rNR3R3a, (CH2)rC(O)R3, NR3C(O)R3a, C(O)NR3R3a, NR3C(O)NR3R3a, CH(═NR3)NR3R3a, NH3C(═NR3)NR3R3a, SO2NR3R3a, NR3SO2NR3R3a, NR3SO2-C1-4 alkyl, NR3SO2CF3, NR3SO2-phenyl, S(O)pCF3, S(O)p-C1-4 alkyl, S(O)p-phenyl, and (CF2)rCF3;
R5, at each occurrence, is selected from CF3, C1-6 alkyl, phenyl substituted with 0-2 R6, and benzyl substituted with 0-2 R6;
R6, at each occurrence, is selected from H, OH, (CH2)rOR2, halo, C1-4 alkyl, CN, NO2, (CH2)rNR2R2a, (CH2)rC(O)R2b, NR2C(O)R2b, NR2C(O)NR2R2a, CH(═NH)NH2, NHC(═NH)NH2, SO2NR2R2a, NR2SO2NR2R2a, and NR2SO2C1-4 alkyl;
R7, at each occurrence, is selected from H, OH, C1-6 alkyl, C1-6 alkylcarbonyl, C1-6 alkoxy, C1-4 alkoxycarbonyl, (CH2)n-phenyl, C6-10 aryloxy, C6-10 aryloxycarbonyl, C6-10 arylmethylcarbonyl, C1-4 alkylcarbonyloxy C1-4 alkoxycarbonyl, C6-10 arylcarbonyloxy C1-4 alkoxycarbonyl, C1-6 alkylaminocarbonyl, phenylaminocarbonyl, and phenyl C1-4 alkoxycarbonyl;
R8, at each occurrence, is selected from H, C1-6 alkyl and (CH2)n-phenyl;
alternatively, R7 and R8 combine to form a 5 or 6 membered saturated, ring which contains from 0-1 additional heteroatoms selected from the group consisting of N, O, and S;
R9, at each occurrence, is selected from H, C1-6 alkyl and (CH2)n-phenyl;
n, at each occurrence, is selected from 0, 1, 2, and 3;
m, at each occurrence, is selected from 0, 1, and 2;
p, at each occurrence, is selected from 0, 1, and 2;
q, at each occurrence is selected from 1 and 2;
r, at each occurrence, is selected from 0, 1, 2, and 3;
s, at each occurrence, is selected from 0, 1, and 2; and,
t, at each occurrence, is selected from 0 and 1.
2. A compound according to
claim 1
, wherein the compound is of formula Ia or Ib:
Figure US20010000179A1-20010405-C00028
wherein;
Z is selected from a CH2O, OCH2, CH2NH, NHCH2, C(O), CH2C(O), C(O)CH2, NHC(O), C(O)NH, CH2S(O)2, S(O)2(CH2), SO2NH, and NHSO2, provided that Z does not form a N—N, N—O, NCH2N, or NCH2O bond with group A;
A is selected from one of the following carbocyclic and heterocyclic systems which are substituted with 0-2 R4;
phenyl, piperidinyl, piperazinyl, pyridyl, pyrimidyl, furanyl, morpholinyl, thiophenyl, pyrrolyl, pyrrolidinyl, oxazolyl, isoxazolyl, thiazolyl, isothiazolyl, pyrazolyl, imidazolyl, oxadiazolyl, thiadiazolyl, triazolyl, 1,2,3-oxadiazolyl, 1,2,4-oxadiazolyl, 1,2,5-oxadiazolyl, 1,3,4-oxadiazolyl, 1,2,3-thiadiazolyl, 1,2,4-thiadiazolyl, 1,2,5-thiadiazolyl, 1,3,4-thiadiazolyl, 1,2,3-triazolyl, 1,2,4-triazolyl, 1,2,5-triazolyl, 1,3,4-triazolyl, benzofuranyl, benzothiofuranyl, indolyl, benzimidazolyl, benzoxazolyl, benzthiazolyl, indazolyl, benzisoxazolyl, benzisothiazolyl, and isoindazolyl;
B is selected from: Y, X—Y, NR2R2a, C(═NR2)NR2R2a, and NR2C(═NR2)NR2R2a;
X is selected from C1-4 alkylene, —C(O)—, —C(═NR)—, —CR2(NR2R2a)—, —C(O)CR2R2a—, —CR2R2aC(O), —C(O)NR2—, —NR2C(O)—, —C(O)NR2CR2R2a—, —NR2C(O)CR2R2a—, —CR2R2aC(O)NR2—, —CR2R2aNR2C(O)—, —NR2C(O)NR2—, —NR2—, —NR2CR2R2a—, —CR2R2aNR2—, O, —CR2R2aO—, and —OCR2R2a—;
Y is NR2R2a, provided that X—Y do not form a N—N or O—N bond;
alternatively, Y is selected from one of the following carbocyclic and heterocyclic systems which are substituted with 0-2 R4a;
cylcopropyl, cyclopentyl, cyclohexyl, phenyl, piperidinyl, piperazinyl, pyridyl, pyrimidyl, furanyl, morpholinyl, thiophenyl, pyrrolyl, pyrrolidinyl, oxazolyl, isoxazolyl, isoxazolinyl, thiazolyl, isothiazolyl, pyrazolyl, imidazolyl, oxadiazolyl, thiadiazolyl, triazolyl, 1,2,3-oxadiazolyl, 1,2,4-oxadiazolyl, 1,2,5-oxadiazolyl, 1,3,4-oxadiazolyl, 1,2,3-thiadiazolyl, 1,2,4-thiadiazolyl, 1,2,5-thiadiazolyl, 1,3,4-thiadiazolyl, 1,2,3-triazolyl, 1,2,4-triazolyl, 1,2,5-triazolyl, 1,3,4-triazolyl, benzofuranyl, benzothiofuranyl, indolyl, benzimidazolyl, benzoxazolyl, benzthiazolyl, indazolyl, benzisoxazolyl, benzisothiazolyl, and isoindazolyl;
alternatively, Y is selected from the following bicyclic heteroaryl ring systems:
Figure US20010000179A1-20010405-C00029
K is selected from O, S, NH, and N.
3. A compound according to
claim 2
, wherein;
Z is selected from a C(O), CH2C(O), C(O)CH2, NHC(O), C(O)NH, C(O)N(CH3), CH2S(O)2, S(O)2(CH2), SO2NH, and NHSO2, provided that Z does not form a N—N or NCH2N bond with group A.
4. A compound according to
claim 3
, wherein;
E is phenyl substituted with R or 2-pyridyl substituted with R;
D is selected from C(O)NH2, C(═NH)NH2, CH2NH2, CH2NHCH3, CH(CH3)NH2, and C(CH3)2NH2; and,
R is selected from H, OCH3, Cl, and F.
5. A compound according to
claim 4
, wherein;
D—E is selected from 3-amidinophenyl, 3-aminomethylphenyl, 3-aminocarbonylphenyl, 3-(methylaminomethyl)phenyl, 3-(1-aminoethyl)phenyl, 3-(2-amino-2-propyl)phenyl, 4-chloro-3-amidinophenyl, 4-chloro-3-aminomethylphenyl, 4-chloro-3-(methylaminomethyl)phenyl, 4-fluoro-3-amidinophenyl, 4-fluoro-3-aminomethylphenyl, 4-fluoro-3-(methylaminomethyl)phenyl, 6-amidinopyrid-2-yl, 6-aminomethylpyrid-2-yl, 6-aminocarbonylpyrid-2-yl, 6-(methylaminomethyl)pyrid-2-yl, 6-(1-aminoethyl)pyrid-2-yl, and 6-(2-amino-2-propyl)pyrid-2-yl.
6. A compound according to
claim 3
, wherein;
Z is C(O)CH2 and CONH, provided that Z does not form a N—N bond with group A;
A is selected from phenyl, pyridyl, and pyrimidyl, and is substituted with 0-2 R4; and,
B is selected from X—Y, phenyl, pyrrolidino, morpholino, 1,2,3-triazolyl, and imidazolyl, and is substituted with 0-1 R4a;
R4, at each occurrence, is selected from OH, (CH2)rOR2, halo, C1-4 alkyl, (CH2)rNR2R2a, and (CF2)rCF3;
R4a is selected from C1-4 alkyl, CF3, S(O)pR5, SO2NR2R2a, and 1-CF3-tetrazol-2-yl;
R5, at each occurrence, is selected from CF3, C1-6 alkyl, phenyl, and benzyl;
X is CH2 or C(O); and,
Y is selected from pyrrolidino and morpholino.
7. A compound according to
claim 6
, wherein;
A is selected from the group: phenyl, 2-pyridyl, 3-pyridyl, 2-pyrimidyl, 2-Cl-phenyl, 3-Cl-phenyl, 2-F-phenyl, 3-F-phenyl, 2-methylphenyl, 2-aminophenyl, and 2-methoxyphenyl; and,
B is selected from the group: 2-CF3-phenyl, 2-(aminosulfonyl)phenyl, 2-(methylaminosulfonyl)phenyl, 2-(dimethylaminosulfonyl)phenyl, 1-pyrrolidinocarbonyl, 2-(methylsulfonyl)phenyl, 4-morpholino, 2-(1′-CF3-tetrazol-2-yl)phenyl, 4-morpholinocarbonyl, 2-methyl-1-imidazolyl, 5-methyl-1-imidazolyl, 2-methylsulfonyl-1-imidazolyl and, 5-methyl-1,2,3-triazolyl.
8. A compound according to
claim 3
, wherein;
E is phenyl substituted with R or 2-pyridyl substituted with R;
D is selected from C(O)NH2, C(═NH)NH2, CH2NH2, CH2NHCH3, CH(CH3)NH2, and C(CH3)2NH2; and,
R is selected from H, OCH3, Cl, and F;
Z is C(O)CH2 and CONH, provided that Z does not form a N—N bond with group A;
A is selected from phenyl, pyridyl, and pyrimidyl, and is substituted with 0-2 R4; and,
B is selected from X—Y, phenyl, pyrrolidino, morpholino, 1,2,3-triazolyl, and imidazolyl, and is substituted with 0-1 R4a;
R4, at each occurrence, is selected from OH, (CH2)rOR2, halo, C1-4 alkyl, (CH2)rNR2R2a, and (CF2)rCF3;
R4a is selected from C1-4 alkyl, CF3, S(O)pR5, SO2NR2R2a, and 1-CF3-tetrazol-2-yl;
R5, at each occurrence, is selected from CF3, C1-6 alkyl, phenyl, and benzyl;
X is CH2 or C(O); and,
Y is selected from pyrrolidino and morpholino.
9. A compound according to
claim 8
 wherein;
D—E is selected from 3-amidinophenyl, 3-aminomethylphenyl, 3-aminocarbonylphenyl, 3-(methylaminomethyl)phenyl, 3-(1-aminoethyl)phenyl, 3-(2-amino-2-propyl)phenyl, 4-chloro-3-amidinophenyl, 4-chloro-3-aminomethylphenyl, 4-chloro-3-(methylaminomethyl)phenyl, 4-fluoro-3-amidinophenyl, 4-fluoro-3-aminomethylphenyl, 4-fluoro-3-(methylaminomethyl)phenyl, 6-amidinopyrid-2-yl, 6-aminomethylpyrid-2-yl, 6-aminocarbonylpyrid-2-yl, 6-(methylaminomethyl)pyrid-2-yl, 6-(1-aminoethyl)pyrid-2-yl, 6-(2-amino-2-propyl)pyrid-2-yl;
A is selected from the group: phenyl, 2-pyridyl, 3-pyridyl, 2-pyrimidyl, 2-Cl-phenyl, 3-Cl-phenyl, 2-F-phenyl, 3-F-phenyl, 2-methylphenyl, 2-aminophenyl, and 2-methoxyphenyl; and,
B is selected from the group: 2-CF3-phenyl, 2-(aminosulfonyl)phenyl, 2-(methylaminosulfonyl)phenyl, 2-(dimethylaminosulfonyl)phenyl, 1-pyrrolidinocarbonyl, 2-(methylsulfonyl)phenyl, 4-morpholino, 2-(1′-CF3-tetrazol-2-yl)phenyl, 4-morpholinocarbonyl, 2-methyl-1-imidazolyl, 5-methyl-1-imidazolyl, 2-methylsulfonyl-1-imidazolyl and, 5-methyl-1,2,3-triazolyl.
10. A compound according to
claim 9
, wherein the compound is of formula Ia.
11. A compound according to
claim 9
, wherein the compound is of formula Ib.
12. A compound according to
claim 3
, wherein;
D is selected from C(═NR8)NR7R9, C(O)NR7R8, NR7R8, and CH2NR7R8;
E is phenyl substituted with R or pyridyl substituted with R;
R is selected from H, Cl, F, OR3, CH3, CH2CH3, OCF3, and CF3;
Z is selected from C(O), CH2C(O), C(O)CH2, NHC(O), and C(O)NH, provided that Z does not form a N—N bond with group A;
R1a and R1b are, at each occurrence, independently selected from H, —(CH2)r—R1′, NCH2R1″, OCH2R1″, SCH2R1″, N(CH2)2(CH2)tR1′, O(CH2)2(CH2)tR1′, and S(CH2)2(CH2)tR1′;
R1c is selected from H, —(CH2)q—R1′, C1-3 alkyl, C(O)R2c, (CF2)rCO2R2c, and C(O)NR2R2a;
R1′, at each occurrence, is selected from H, C1-3 alkyl, halo, (CF2)rCF3, OR2, NR2R2a, C(O)R2c, (CF2)rCO2R2c, S(O)pR2b, NR2(CH2)rOR2, NR2C(O)R2b, NR2C(O)2R2b, C(O)NR2R2a, SO2NR2R2a, and NR2SO2R2b;
A is selected from one of the following carbocyclic and heterocyclic systems which are substituted with 0-2 R4;
phenyl, piperidinyl, piperazinyl, pyridyl, pyrimidyl, furanyl, morpholinyl, thiophenyl, pyrrolyl, pyrrolidinyl, oxazolyl, isoxazolyl, thiazolyl, isothiazolyl, pyrazolyl, and imidazolyl;
B is selected from: Y, X—Y, NR2R2a, C(═NR2)NR2R2a, and NR2C(═NR2)NR2R2a;
X is selected from CH2, —CR2(CR2R2b)(CH2)t—, —C(O)—, —C(═NR)—, —CH(NR2R2a)—, —C(O)NR2—, —NR2C(O)—, —NR2C(O)NR2—, —NR2—, and O;
Y is NR2R2a, provided that X—Y do not form a N—N or O—N bond;
alternatively, Y is selected from one of the following carbocyclic and heterocyclic systems which are substituted with 0-2 R4a;
phenyl, piperidinyl, piperazinyl, pyridyl, pyrimidyl, furanyl, morpholinyl, thiophenyl, pyrrolyl, pyrrolidinyl, oxazolyl, isoxazolyl, isoxazolinyl, thiazolyl, isothiazolyl, pyrazolyl, imidazolyl, oxadiazolyl, thiadiazolyl, triazolyl, 1,2,3-oxadiazolyl, 1,2,4-oxadiazolyl, 1,2,5-oxadiazolyl, 1,3,4-oxadiazolyl, 1,2,3-thiadiazolyl, 1,2,4-thiadiazolyl, 1,2,5-thiadiazolyl, 1,3,4-thiadiazolyl, 1,2,3-triazolyl, 1,2,4-triazolyl, 1,2,5-triazolyl, and 1,3,4-triazolyl;
R4, at each occurrence, is selected from ═O, OH, Cl, F, C1-4 alkyl, (CH2)rNR2R2a, (CH2)rC(O)R2b, NR2C(O)R2b, C(O)NR2R2a, CH(═NH)NH2, NHC(═NH)NH2, SO2NR2R2a, NR2SO2-C1-4 alkyl, NR2SO2R5, S(O)pR5, and (CF2)rCF3;
R4a, at each occurrence, is selected from ═O, OH, Cl, F, C1-4 alkyl, (CH2)rNR2R2a, (CH2)rC(O)R2b, NR2C(O)R2b, C(O)NR2R2a, CH(═NH)NH2, NHC(═NH)NH2, SO2NR2R2a, NR2SO2-C1-4 alkyl, NR2SO2R5, S(O)pR5, (CF2)rCF3, and 1-CF3-tetrazol-2-yl;
R5, at each occurrence, is selected from CF3, C1-6 alkyl, phenyl substituted with 0-2 R6, and benzyl substituted with 0-2 R6;
R6, at each occurrence, is selected from H, ═O, OH, OR2, Cl, F, CH3, CN, NO2, (CH2)rNR2R2a, (CH2)rC(O)R2b, NR2C(O)R2b, CH(═NH)NH2, NHC(═NH)NH2, and SO2NR2R2a;
R7, at each occurrence, is selected from H, OH, C1-6 alkyl, C1-6 alkylcarbonyl, C1-6 alkoxy, C1-4 alkoxycarbonyl, benzyl, C6-10 aryloxy, C6-10 aryloxycarbonyl, C6-10 arylmethylcarbonyl, C1-4 alkylcarbonyloxy C1-4 alkoxycarbonyl, C6-10 arylcarbonyloxy C1-4 alkoxycarbonyl, C1-6 alkylaminocarbonyl, phenylaminocarbonyl, and phenyl C1-4 alkoxycarbonyl;
R8, at each occurrence, is selected from H, C1-6 alkyl and benzyl; and
alternatively, R7 and R8 combine to form a morpholino group; and,
R9, at each occurrence, is selected from H, C1-6 alkyl and benzyl.
13. A compound according to
claim 12
, wherein;
E is phenyl substituted with R or 2-pyridyl substituted with R;
R is selected from H, Cl, F, OCH3, CH3, OCF3, and CF3;
Z is selected from a C(O)CH2 and C(O)NH, provided that Z does not form a N—N bond with group A;
R1a, at each occurrence, is selected from H, CH3, CH2CH3, Cl, F, CF3, OCH3, NR2R2a, S(O)pR2b, CH2S(O)pR2b, CH2NR2S(O)pR2b, C(O)R2c, CH2C(O)R2c, C(O)NR2R2a, and SO2NR2R2a;
R1b is selected from H, CH3, CH2CH3, Cl, F, CF3, OCH3, NR2R2a, S(O)pR2b, CH2S(O)pR2b, CH2NR2S(O)pR2b, C(O)R2c, CH2C(O)R2c, C(O)NR2R2a, and SO2NR2R2a;
R1c is selected from H, CH3, CH2CH3, CF3, CH2S(O)pR2b, CH2NR2S(O)pR2b, C(O)R2c, CH2C(O)R2c, and C(O)NR2R2a;
A is selected from one of the following carbocyclic and heterocyclic systems which are substituted with 0-2 R4;
phenyl, pyridyl, pyrimidyl, furanyl, thiophenyl, pyrrolyl, oxazolyl, isoxazolyl, thiazolyl, isothiazolyl, pyrazolyl, and imidazolyl;
B is selected from: Y and X—Y;
X is selected from CH2, —CR2(CR2R2b)—, —C(O)—, —C(═NR)—, —CH(NR2R2a)—, —C(O)NR2—, —NR2C(O)—, —NR2C(O)NR2—, —NR2—, and O;
Y is NR2R2a, provided that X—Y do not form a N—N or O—N bond;
alternatively, Y is selected from one of the following carbocyclic and heterocyclic systems which are substituted with 0-2 R4a;
phenyl, piperidinyl, piperazinyl, pyridyl, pyrimidyl, furanyl, morpholinyl, thiophenyl, pyrrolyl, pyrrolidinyl, oxazolyl, isoxazolyl, isoxazolinyl, thiazolyl, isothiazolyl, pyrazolyl, imidazolyl, oxadiazolyl, thiadiazolyl, triazolyl, 1,2,3-oxadiazolyl, 1,2,4-oxadiazolyl, 1,2,5-oxadiazolyl, 1,3,4-oxadiazolyl, 1,2,3-thiadiazolyl, 1,2,4-thiadiazolyl, 1,2,5-thiadiazolyl, 1,3,4-thiadiazolyl, 1,2,3-triazolyl, 1,2,4-triazolyl, 1,2,5-triazolyl, and 1,3,4-triazolyl;
R2, at each occurrence, is selected from H, CF3, CH3, benzyl, and phenyl;
R2a, at each occurrence, is selected from H, CF3, CH3, benzyl, and phenyl;
R2b, at each occurrence, is selected from CF3, OCH3, CH3, benzyl, and phenyl;
R2c, at each occurrence, is selected from CF3, OH, OCH3, CH3, benzyl, and phenyl;
alternatively, R2 and R2a combine to form a 5 or 6 membered saturated, partially unsaturated, or unsaturated ring which contains from 0-1 additional heteroatoms selected from the group consisting of N, O, and S;
R3, at each occurrence, is selected from H, CH3, CH2CH3, and phenyl;
R3a, at each occurrence, is selected from H, CH3, CH2CH3, and phenyl;
R4, at each occurrence, is selected from OH, Cl, F, CH3, CH2CH3, NR2R2a, CH2NR2R2a, C(O)R2b, NR2C(O)R2b, C(O)NR2R2a, and CF3;
R4a, at each occurrence, is selected from OH, Cl, F, CH3, CH2CH3, NR2R2a, CH2NR2R2a, C(O)R2b, C(O)NR2R2a, SO2NR2R2a, S(O)pR5, CF3, and 1-CF3-tetrazol-2-yl;
R5, at each occurrence, is selected from CF3, C1-6 alkyl, phenyl substituted with 0-2 R6, and benzyl substituted with 1 R6;
R6, at each occurrence, is selected from H, OH, OCH3, Cl, F, CH3, CN, NO2, NR2R2a, CH2NR2R2a, and SO2NR2R2a;
R7, at each occurrence, is selected from H, OH, C1-3 alkyl, C1-3 alkylcarbonyl, C1-3 alkoxy, C1-4 alkoxycarbonyl, benzyl, phenoxy, phenoxycarbonyl, benzylcarbonyl, C1-4 alkylcarbonyloxy C1-4 alkoxycarbonyl, phenylcarbonyloxy C1-4 alkoxycarbonyl, C1-6 alkylaminocarbonyl, phenylaminocarbonyl, and phenyl C1-4 alkoxycarbonyl;
R8, at each occurrence, is selected from H, CH3, and benzyl; and,
alternatively, R7 and R8 combine to form a morpholino group;
R9, at each occurrence, is selected from H, CH3, and benzyl.
14. A compound according to
claim 13
, wherein;
R1a, at each occurrence, is selected from H, CH3, CH2CH3, Cl, F, CF3, OCH3, NR2R2a, S(O)pR2b, C(O)NR2R2a, CH2S(O)pR2b, CH2NR2S(O)pR2b, C(O)R2c, CH2C(O)R2c, and SO2NR2R2a;
R1b is selected from H, CH3, CH2CH3, Cl, F, CF3, OCH3, NR2R2a, S(O)pR2b, C(O)NR2R2a, CH2S(O)pR2b, CH2NR2S(O)pR2b, C(O)R2b, CH2C(O)R2b, and SO2NR2R2a;
R1c is selected from H, CH3, CH2CH3, CF3, C(O)NR2R2a, CH2S(O)pR2b, CH2NR2S(O)pR2b, C(O)R2b, and CH2C(O)R2b;
A is selected from one of the following carbocyclic and heterocyclic systems which are substituted with 0-2 R4;
phenyl, pyridyl, and pyrimidyl;
B is selected from: Y and X—Y;
X is selected from —C(O)— and O;
Y is NR2R2a, provided that X—Y do not form a O—N bond;
alternatively, Y is selected from one of the following carbocyclic and heterocyclic systems which are substituted with 0-2 R4a;
phenyl, piperazinyl, pyridyl, pyrimidyl, morpholinyl, pyrrolidinyl, imidazolyl, and 1,2,3-triazolyl;
R2, at each occurrence, is selected from H, CF3, CH3, benzyl, and phenyl;
R2a, at each occurrence, is selected from H, CF3, CH3, benzyl, and phenyl;
R2b, at each occurrence, is selected from CF3, OCH3, CH3, benzyl, and phenyl;
R2c, at each occurrence, is selected from CF3, OH, OCH3, CH3, benzyl, and phenyl;
alternatively, R2 and R2a combine to form a ring system selected from pyrrolidinyl, piperazinyl and morpholino;
R4, at each occurrence, is selected from Cl, F, CH3, NR2R2a, and CF3;
R4a, at each occurrence, is selected from Cl, F, CH3, SO2NR2R2a, S(O)pR5, and CF3; and,
R5, at each occurrence, is selected from CF3 and CH3.
15. A compound according to
claim 1
, wherein the compound is selected from the group:
1-(3-amidinophenyl)-5-[[(2′-methylsulfonyl-[1,1′]-biphen-4-yl)-aminocarbonyl]-3-trifluoromethyl-pyrazoline; and,
1-(3-aminomethylphenyl)-5-[[(2′-methylsulfonyl-[1,1′]-biphen-4-yl)-aminocarbonyl]-3-trifluoromethyl-pyrazoline;
and pharmaceutically acceptable salts thereof.
16. A pharmaceutical composition, comprising: a pharmaceutically acceptable carrier and a therapeutically effective amount of a compound according to
claim 1
 or a pharmaceutically acceptable salt thereof.
17. A method for treating or preventing a thromboembolic disorder, comprising: administering to a patient in need thereof a therapeutically effective amount of a compound according to
claim 1
 or a pharmaceutically acceptable salt thereof.
US09/728,695 1998-03-27 2000-12-01 Disubstituted pyrazolines and triazolines as factor Xa inhibitors Expired - Lifetime US6436985B2 (en)

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