EP0689545A4 - Macrocyclic amide and urea immunomodulators - Google Patents

Macrocyclic amide and urea immunomodulators

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Publication number
EP0689545A4
EP0689545A4 EP94910923A EP94910923A EP0689545A4 EP 0689545 A4 EP0689545 A4 EP 0689545A4 EP 94910923 A EP94910923 A EP 94910923A EP 94910923 A EP94910923 A EP 94910923A EP 0689545 A4 EP0689545 A4 EP 0689545A4
Authority
EP
European Patent Office
Prior art keywords
compound
ethyl
configuration
och2c
attaches
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP94910923A
Other languages
German (de)
French (fr)
Other versions
EP0689545A1 (en
Inventor
Rolf Wagner
Jay R Luly
Yat Sun Or
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Abbott Laboratories
Original Assignee
Abbott Laboratories
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Filing date
Publication date
Application filed by Abbott Laboratories filed Critical Abbott Laboratories
Publication of EP0689545A1 publication Critical patent/EP0689545A1/en
Publication of EP0689545A4 publication Critical patent/EP0689545A4/en
Withdrawn legal-status Critical Current

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/12—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains three hetero rings
    • C07D498/18—Bridged systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04—Antibacterial agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/02—Immunomodulators
    • A61P37/06—Immunosuppressants, e.g. drugs for graft rejection

Definitions

  • the present invention relates to novel chemical compounds having immunomodulatory activity, and in particular to macrolide immunosuppressants. More particularly, the invention relates to semisynthetic analogs of ascomycin and FK-506, to means for their preparation, to pharmaceutical compositions containing such compounds and to methods of treatment employing the same.
  • cyclosporine (cyclosporin A) has found wide use since its introduction in the fields of organ transplantation and immunomodulation, and has brought about a significant increase in the success rate for transplantation procedures.
  • FR-900520 also known as ascomycin, has been previously disclosed by Arai et al. in U.S. Patent No. 3,244,592, issued April 5, 1966, where the compound is described as an antifungal agent.
  • Monaghan, R.L., et al . describe the use of ascomycin as an immunosuppressant in European Patent Application No. 323865, published July 12, 1989.
  • the immunosuppressive activity of FK-506 has been clinically confirmed, its toxicity in mammals has limited its utility.
  • the activity of FK-506 has, however, prompted efforts to discover novel analogs of FK-type compounds which possess superior properties. These efforts include the isolation of new fermentation products, the microbial transformation of existing chemical entities, the chemical modification of these macrocyples, and the synthesis of hybrid species derived from smaller synthetic fragments.
  • Fermentation products of FK-type compounds include C-21-epi derivatives of FK- 506; a 31-demethylated derivative of FK-506; 31-oxo-FK-506; and compounds derived from FK-506, FR-900523 and FR-900525 which are characterized by the introduction of hydroxy- protecting groups, formation of a double bond by elimination of water between carbons 23 and 24, oxidation of the hydroxy group at carbon 24 to the ketone, and reduction of the allyl side-chain at carbon 21 via hydrogenation.
  • Other published derivatives include those derived from FK-506 and FR-900520 where the lactone ring is contracted to give a macrocyclic ring containing two fewer carbons.
  • FK-type compounds Numerous chemical modifications of the FK-type compounds have been attempted. These include the preparation of small synthetic fragments of FK-type derivatives; a thermal rearrangement of a variety of derivatives of FK-506 which expands the macrocyclic ring by two carbons; and modifications which include methyl ether and aryl ether formation at C-32 and/or C-24, oxidation of C-32 alcohol to the ketone, and epoxide formation at C-9.
  • one object of the invention is to provide novel semisynthetic macrolides which possess the desired immunomodulatory activity but which minimize undesired side effects.
  • Another object of the present invention is to provide synthetic processes for the preparation of such compounds from starting materials obtained by fermentation, as well as chemical intermediates useful in such synthetic processes.
  • a further object of the invention is to provide pharmaceutical compositions containing, as an active ingredient, one of the above compounds.
  • Yet another object of the invention is to provide a method of treating a variety of disease states, including post- transplant tissue rejection and autoimmune disfunction.
  • the present invention is directed to compounds having the formula:
  • n, R, R 1 , R la > R 2 , R 2a , R 3 , R 4 and R 5 are specifically defined, which possess immunosuppressive, antimicrobial, antifungal, antiviral, antunflammatory and antiproliferative activity, as well as the ability to reverse chemotherapeutic drug resistance; to pharmaceutical compositions comprising a compound of the invention in combination with a pharmaceutically-acceptable carrier; to processes for the preparation of these compounds; to synthetic intermediates useful in the preparations of these and other immunomodulator derivatives of ascomycin; to methods of formulating pharmaceutical compositions comprising these compounds; and to a method of immunomodulatory treatment of a human or veterinary subject in need of such treatment by the administration of a therapeutically-effective amount of a novel compound according to the present invention.
  • n zero or one
  • R is hydrogen, methyl, ethyl, allyl, propyl, 2-hydroxyethyl, cyclopropylmethyl, 2-oxopropyl or 2-ethanal;
  • R 1 and R la are selected such that one of R 1 and R la is hydrogen, -(C1-C6- alkyl)oxy or hydroxy, and the other is chosen from the group consisting of: (I) -O(CH )jC(O)R 12 , where j is one-to-five, and Rl 2 is:
  • aryl-(C ⁇ -C6-alkyl)- where aryl is as defined below, wherein the zero, one, two or three substituents on the aryl group, each designated R 301 , are independently selected from the group consisting of:
  • R 400 is selected from the group consisting of: a. mod-aryl, as defined below, wherein the one, two, or three substituents, each designated R 302 , are independently selected from the group consisting of:
  • NR 18 R 19 is either a nitrogen atom attached to R18 and R 19 , wherein Rl» and R* 9 are independently selected from the group consisting of hydrogen, -(Ci- C6-alkyl), unsubstituted aryl-, and unsubstituted aryl-(C ⁇ -C6-alkyl); or NR!8R 19 may be a 3-to- 7-membered heterocyclic ring comprising ring carbon atoms, the nitrogen atom shown, and zero, one or two additional heteroatoms independently selected from the group consisting of -O-, -NH-, -N(C ⁇ -to-C 6 -alkyl) and -S(O) s -, wherein s is zero, one or two;
  • R 10 is: (i) -PO(OH)O-M+, wherein M + is a proton or a positively charged inorganic or organic counterion, as defined below, (ii) -SO3"M + , wherein M + is as defined above, (iii) -C(O)(CH 2 ) m C(O)O-M+, wherein m and M + are as defined above;
  • any two adjacent R 302 substituents in a di- or trisubstituted mod-aryl group form a 5-, 6- or 7- membered carbocyclic ring or a 5-, 6- or 7-membered heterocyclic ring wherein " the ring atoms consist of carbon atoms and one or two heteroatoms independently selected from the group consisting of -O-, -S(O) s -, where s
  • -NR 8 R 9 may be a 3- to 7-membered heterocyclic ring, where the ring consists of carbon atoms, the nitrogen atom shown, and zero, one or two additional heteroatoms independendy selected from the group consisting of -O-, -S(O) s -, wherein s is as defined above, and -NR 8 -, wherein R 8 is as defined above;
  • any two adjacent R 301 substituents in a di- or trisubstituted aryl group form a 5-, 6- or 7-membered carbocyclic ring or a 5-, 6- or 7-membered heterocyclic ring wherein the ring atoms consist of carbon atoms and zero, one or two heteroatoms independently selected from the group consisting of -O-, -S(O) s -, where s is as defined above, and -NR 8 -
  • R 6 is selected from the group consisting of:
  • -NR 6 R 7 may be a 3- to 7-membered heterocyclic ring, where the ring consists of carbon atoms, the nitrogen atom shown, and zero, one, or two additional heteroatoms independently selected from the group consisting of -O-, -S(O) s -, wherein s is as defined above, and -NR 8 -, wherein R 8 is as defined above, which ring is unsubstituted or substituted with from one-to-six compatible radicals independently selected from the group consisting of:
  • R 399 is selected from the group consisting of:
  • each R 11 is independently -(Ci-C ⁇ -alkyl), aryl-(C ⁇ -C6- alkyl)-, or aryl;
  • (M) halogen; (II) -O(CH 2 ) m S(O) s R 12 , where m, s and R 12 are as defined above; (HI) -O(CH 2 ) j CN, where j is as defined above; (TV) -O(CH 2 ) j C( NOR 14 )R 12 , where j, R 12 and R 14 are as defined above;
  • R 2 and R 2a are independently hydrogen, halogen, or -OR 14 , wherein R 14 is as defined above, or one of R 2 and R 2 * 1 may be hydroxy, when the other of R 2 or R 21 is hydrogen, or R 2 and R 23 taken together is oxo or thiooxo;
  • R 3 and R 4 are chosen, when R 5 is hydrogen, such that one of R 3 and R 4 is hydrogen and the other is selected from hydrogen, hydroxy, -OCOR 8 , where R 8 is as defined above, or -OSi(R 11 )3, where each R 11 is independently as defined above, or one of R 3 and R 4 is joined with non-hydrogen R 5 to form a C-23/C-24 bond, with the other being hydrogen, hydroxy, -OCOR 8 , where R 8 is as defined above, or -OSi(R 11 )3, where each R 11 is independently as defined above;
  • R 5 is hydrogen, or taken together with either R 3 or R 4 , forms a C-23/C-24 bond.
  • R 1 may not be defined as, (I)-O(CH 2 )jC(O)R 20 , where j is as defined above and R 20 is selected from
  • R 21 is loweralkyl, cycloalkyl, cycloalkylalkyl or qualified- arylalkyl, where qualified-arylalkyl is defined below;
  • NR 22 R 23 is either: a nitrogen atom attached to R 22 and R 23 , where R 22 is selected from hydrogen, loweralkyl, qualified-arylalkyl, cycloalkyl and cycloalkylalkyl; and R 23 is selected from hydrogen, loweralkyl, qualified-arylalkyl, cycloalkyl, cycloalkylalkyl, aminoalkyl, hydroxyalkyl, carboxyalkyl, and thioloweralkyl; or a saturated heterocyclic ring, where taken together, R 22 and R 23 are
  • R 24 and R 25 are -(CH 2 )p-, wherein p is two to five; or ( ⁇ i) -O(CH 2 )jC(O)N(R )(CH 2 ) m CH(R 2 5)C(O)R 20 , where j, m and R 20 are as defined above and R 24 is selected from hydrogen, loweralkyl, qualified-arylalkyl, cycloalkyl and cycloalkylalkyl; and R 25 is selected from hydrogen, loweralkyl, hydroxyloweralkyl, carboxyalkyl, thioloweralkyl, thioalkoxyalkyl, guanidinoalkyl, aminoalkyl, qualified-arylalkyl and, if m is other than zero, amino or amidoalkyl; or taken together, R 24 and R 25 are -(CH 2 )p-, wherein p is two to five; or ( ⁇ i) -O(CH 2 )jC(O)N(
  • R 28 is selected from hydrogen, loweralkyl, qualified-arylalkyl, cycloalkyl and cycloalkylalkyl
  • R 29 is selected from hydrogen, loweralkyl, hydroxyloweralkyl, carboxyalkyl, thioloweralkyl, thioalkoxyalkyl, guanidinoalkyl, aminoalkyl, qualified-arylalkyl and, if m2 is other than zero, amino or amidoalkyl; or taken together, R 28 and R 29 are -(CH )p-, wherein p is as defined above.
  • n, R, R 2 , R 23 , R 3 , R 4 and R 5 are as defined above and A is selected from among: , where j, R 12 ,
  • R 13 , R 14 and R 15 are as defined above.
  • n, R, R 2 , R 2a , R 3 , R 4 and R 5 are as defined above and B is selected from:
  • n, R, R 2 , R 2 , R 3 , R 4 and R 5 are as defined above and D is selected from:
  • Preferred compounds according to the invention are the compounds of:
  • More preferred compounds according to the invention are the compounds of:
  • Acyl refers to an aryl or alkyl group, as defined below, appended to the remainder of the molecule via a carbonyl group. Examples include, but are not limited to, acetyl, pivaloyl, benzoyl, and the like.
  • Acylamino refers to an acyl group, as defined above, except that it is appended to the remainder of the molecule via an amino group. Examples include, but are not limited to, acetylamino, pivaloylamino, benzoylamino, and the like.
  • Acylguanidino refers to an acyl group, as defined above, except that it is attached to the remainder of the molecule via a nitrogen of a guanidino radical in one of three ways: HN(acyl)C(NH)NH- or H2NC(NH)N(acyl)- or (acyl)NC(NH2)HN-.
  • Alkenyl refers to straight- or branched-chain groups of a specified number of carbon atoms containing at least one carbon-carbon double bond including, but not limited to ethenyl, 1-propenyl, 2-propenyl, 2-methyl-l-propenyl, 1-butenyl, 2-butenyl, and the like.
  • Alkoxy refers to an alkyl group, as defined below, attached to the remainder of the molecule through an oxygen atom. Examples include, but are not limited to, methoxy, ethoxy, isopropoxy, n-butoxy, sec-butoxy, isobutoxy, tert-butoxy and the like.
  • Alkoxycarbonyl refers to an alkoxy group, as defined above, except that it is attached to the remainder of the molecule via a carbonyl group. Examples include, but are not limited to, methyloxycarbonyl, ethyloxycarbonyl, tert-butyloxycarbonyl, cyclohexyloxycarbonyl, and the like.
  • Alkoxycarbonylamino refers to an alkoxycarbonyl group, as defined above, except that it is attached to the remainder of the molecule via an amino group. Examples include, but are not limited to, methyloxy-carbonylamino, tert-butyloxycarbonylamino, and the like.
  • Alkoxycarbonylguanidino refers to an alkoxycarbonyl group, as defined above, except that it is attached to the remainder of the molecule via a nitrogen of a guanidino radical in one of three ways: HN(alkoxycarbonyl)C(NH)HN-, H 2 NC(NH)N(alkoxycarbonyl)- or (alkoxycarb ⁇ nyl)NC(NH 2 )HN-.
  • Alkyl refers to a straight- or branched-chain group of a specified number of carbon atoms including, as appropriate, but not necessarily limited to, methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, and the like.
  • Alkylamino refers to a group having the structure -NH-(alkyl), where the alkyl portion is as defined above, including, for example, methylamino, ethylamino, isopropylamino, and the like.
  • Alkylsulfonyl refers to an alkyl group, as defined above, except that it is attached to the remainder of the molecule via a sulfur dioxide diradical. Examples include but are not limited to, methanesulfonyl, camphorsulfonyl and the like.
  • Alkylthioether and thioalkoxy refer to an alkyl group, as previously defined, except that it is attached to the remainder of the molecule via a sulfur atom. Examples include, but are not limited to, thiomethoxy, thioethoxy, thioisopropoxy, n-thiobutoxy, sec- thiobutoxy, isothiobutoxy, tert-thiobutoxy, and the like.
  • Alkynyl refers to straight- or branched-chain groups of a specified number of carbon atoms containing at least one carbon-carbon triple bond, including, but not limited to acetylenyl, propargyl, and the like.
  • “Amidoalkyl” refers to a group having the structure -NR 1 1 C(O)R 102 appended to the remainder of the molecule via an alkyl group, as previously defined, wherein R101 an d R 102 are independently hydrogen, alkyl, aryl, arylalkyl, or halosubstituted alkyl, or R 10 l and R 02 , taken together, may optionally be -(CH )aa-, where aa is an integer of from 2-to-6.
  • Aminoalkyl refers to a group having the structure -NR 0 3R104 appended to the remainder of the molecule via an alkyl group, as previously defined, wherein R103 and R 104 are independently hydrogen, alkyl, qualified-aryl or qualified-arylalkyl, or Rl°3 and R104, taken together, may optionally be -(CH 2 )bb-, where bb is an integer of from 2-to-6.
  • Aryl refers to mono-, di-, tri- or tetracyclic aromatic groups, charged or uncharged, the rings of which are comprised of from 3-to-7 carbon atoms.
  • aryl include, but are not limited to, phenyl, 1- or 2-naphthyl, azulenyl, fluorenyl, (1, 2)-dihydronaphthyl, (l,2,3,4)-tetrahydronaphthyl, indenyl, indanyl and the like, which are unsubstituted or substituted with from one, two or three independently-selected substituents, R 301 , as defined above.
  • Arylalkoxy and “arylalkylether” refer to an arylalkyl group, as defined below, attached to the parent molecular moiety through an oxygen atom. Examples include, but are not limited to, benzyloxy, 2-phenethyloxy, 1-naphthylmethyloxy, and the like.
  • Arylalkoxycarbonyl refers to an arylalkoxy group, as defined above, except that it is attached to the remainder of the molecule via a carbonyl group. Examples include, but are not limited to, benzyloxycarbonyl, 9-fluorenylmethyloxycarbonyl, and the like.
  • Arylalkoxycarbonylamino refers to an arylalkoxycarbonyl group, as defined above, except that it is attached to the remainder of the molecule via an amino group. Examples include, but are not Umited to, benzyloxycarbonylamino, 9- fluorenylmethyloxycarbonylamino, and the like.
  • Arylalkoxycarbonylguanidino refers to an arylalkoxycarbonyl group, as defined above, except that it is attached to the remainder of the molecule via a nitrogen of a guanidino radical in one of three ways: HN(arylalkoxycarbonyl)C(NH)HN-, H 2 NC(NH)N(arylalkoxycarbonyl)- or (arylalkoxycarbonyl)NC(NH 2 )HN-.
  • Arylalkyl refers to an aryl group, as previously defined, except that it is attached to the remainder of the molecule via an alkyl group.
  • Arylalkylamino refers to a group having the structure -NH- (arylalkyl), where the arylalkyl portion is as previously defined, except that it is attached to the remainder of the molecule via an amino group. Examples include benzylamino, 1-phenylethylamino, and the like.
  • Arylalkylthioether and “thioarylalkoxy” refer to an arylalkyl group, as previously defined, except that it is attached to the remainder of the molecule via a sulfur atom.
  • Arylamino refers to an aryl group, as defined above, except that it is attached to the remainder of the molecule via an amino group. Examples include, but are not limited to, anilino, naphthylamino, and the like.
  • Arylether and "aryloxy” refer to an aryl group, as previously defined, attached to the parent molecular moiety through an oxygen atom. Examples include, but are not limited to, phenoxy, 1-naphthoxy, 2-naphthoxy, and the like.
  • Aryloxycarbonyl refers to an aryloxygroup, as defined above, except that it is attached to the remainder of the molecule via a carbonyl group. Examples include, but are not limited to, phenyloxycarbonyl, and the like.
  • Aryloxycarbonylamino refers to an aryloxycarbonyl group, as defined above, except that it is attached to the remainder of the molecule via an amino group. Examples include, but are not Umited to, phenyloxycarbonylamino, and the like.
  • Aryloxycarbonylguanidino refers to an aryloxycarbonyl group, as defined above, except that it is attached to the remainder of the molecule via a nitrogen of a guanidino moiety in one of three ways: HN(aryloxycarbonyl)C(NH)HN-, H 2 NC(NH)N(aryloxycarbonyl)- or (aryloxycarbonyl)NC(NH 2 )HN-.
  • Arylsulfonyl refers to an aryl group, as defined above, except that it is attached to the remainder of the molecule via a sulfur dioxide group. Examples include, but are not limited to /?-toluenesulfonyl, benzenesulfonyl, and the like.
  • Arylsulfonylguanidino refers to an arylsulfonyl group, as defined above, except that it is attached to the remainder of the molecule via a guanidino group in one of three ways: HN(arylsulfonyl)C(NH)HN- or H 2 NC(NH)N(arylsulfonyl)- or (arylsulfonyl)NC(NH 2 )HN-.
  • Arylthioether and “thioaryloxy” refer to an aryl group, as defined above, except that it is attached to the remainder of the molecule via a sulfur atom.
  • Biaryl refers to a mod-aryl group, as defined below, which carries as a substituent another independently selected mod-aryl group, such that the two are connected by a single carbon-carbon bond.
  • Carboxamido refers to an amino group attached to the remainder of the molecule via a carbonyl group, and having the formula H 2 NC(O)-.
  • Carboxyalkyl refers to a carboxyl group, -CO H, appended to the remainder of the molecule via an alkyl group, as previously defined.
  • Counterion refers to a positively-charged atom or molecular species, with a net charge of +1, which includes, but is not limited to Li + , Na + , Ca(OC(O)CH 3 )+, MgCl+, K+, NH 4 + , (n-butyl) 4 N+, and the like.
  • Cycloalkenyl refers to cyclic groups of 5-to-10 carbons possessing one or more carbon-carbon double bonds including, but not limited to, cyclopentenyl, cyclohexenyl, 1,3,3-trimethylcyclohexenyl, and the like, in which the point of attachment may occur at any available valency on the carbocylic ring.
  • Cycloalkyl refers to saturated cyclic groups of 3-to-8 carbons including, but not limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, and the like.
  • Cycloalkylalkenyl refers to cycloalkyl, as defined above, except that it is attached to the remainder of the molecule via an alkenyl group, as defined above.
  • Cycloalkylalkyl refers to a cycloalkyl group, as defined above, except that it is attached to the remainder of the molecule via an alkyl group. Examples include, but are not limited to, cyclohexylmethyl, cyclohexylethyl, and the like.
  • Cycloalkylalkynyl refers to cycloalkyl, as defined above, except that it is attached to the remainder of the molecule via an alkynyl group, as defined above.
  • Halo and halogen refer to an atom selected from fluorine, chlorine, bromine and iodine.
  • Het- refers to any aromatic 5-, 6- or 7-membered monocyclic ring or a bi- or tri-cycUc group comprising fused five- or six-membered rings having ring carbon atoms and between one and three heteroatoms independently selected from oxygen, sulfur and nitrogen, wherein (i) each 5-membered ring has 2 double bonds and each 6- or 7- membered ring has 3 double bonds, (ii) the nitrogen and sulfur heteroatoms as well as the carbon atoms may optionally be oxidized, (iii) the nitrogen heteroatom may optionaUy be quaternized, (iv) any of these rings may be fused to a benzene ring, and (v) any carbon or heteroatom with suitable valence may bear a substituent, R 301 , as defined above.
  • Any two adjacent R 301 substituents in a di-, tri-, tetra- or penta-substituted Het group may form a 5-, 6- or 7-membered ring consisting of carbon atoms and zero, one or two heteroatoms independently selected from the group consisting of -O-, -S(O) s -, where s is as defined above, and -NR 8 -, where R 8 is as defined above.
  • Het groups include, but are not limited to, pyrrolyl, pyrazolyl, cytosinyl, thiocytosinyl, imidazolyl, pyridyl, pyrazinyl, pyrimidinyl, pyridazinyl, xanthenyl, xanthonyl, xanthopterinyl, oxazolyl, thiouracilyl, isoxazolyl, indolyl, quinolinyl, uracilyl, urazolyl, uricyl, thiazolyl, isothiazolyl, isoquinolinyl, thyminyl, benzimidazolyl, benzothiazolyl, benzoxazolyl, furyl, thienyl, benzothienyl, and the like.
  • Heterocyclic refers to any non- aromatic 5-, 6- or 7-membered monocyclic ring or a bi- or tri-cyclic group comprising fused five- or six-membered rings, having ring carbon atoms and between one-and-three heteroatoms independently selected from oxygen, sulfur and nitrogen, wherein (i) each 5- membered ring has 0 or 1 double bond and each 6-membered ring has 0 to 2 double bonds, (ii) the nitrogen and sulfur heteroatoms as well as the carbon atoms may optionally be oxidized, (iii) the nitrogen heteroatom may optionally be quaternized, (iv) any of these rings may be fused to a benzene ring, and (v) any carbon or heteroatom with suitable valence may bear a substituent, R 301 , as defined above.
  • Any two adjacent R 301 substituents in a di-, tri-, tetra- or penta-substituted heterocyclic group may form a 5-, 6- or 7-membered ring consisting of ring carbon atoms and zero, one or two heteroatoms independently selected from the group consisting of -O-, -S(O) s -, where s is as defined above, and -NR 8 -, where R 8 is as defined above.
  • heterocycles include, but are not Umited to, aziridinyl, thiomorpholine, thiomorpholine-oxide, thiomorpholine dioxide, and pyrrolidinyl, pyrazolinyl, pyrazoUdinyl, imidazolinyl, imidazolidinyl, piperidinyl, piperazinyl, oxazoUdinyl, isoxazoUdinyl, morpholinyl, thiazolidinyl, and isothiazolidinyl, and the like.
  • Heterocyclic alkyl refers to a heterocyclic group, as defined above, except that it is attached to the remainder of the molecule via an alkyl group, as previously defined.
  • HeterocycUc alkylether refers to a heterocycUc alkyl moiety, as defined above, except that it is attached to the remainder of the molecule via an oxygen atom.
  • Heterocyclic alkenyl refers to a heterocyclic group, as defined above, except that it is attached to the remainder of the molecule via an alkenyl group, as previously defined.
  • HeterocycUc alkylthioether refers to a heterocyclic alkyl moiety, as defined above, except that it is attached to the remainder of the molecule via a sulfur atom.
  • Heterocyclic alkynyl refers to a heterocyclic group, as defined above, except that it is attached to the remainder of the molecule via an alkynyl group, as previously defined.
  • Heterocyclic ether refers to a heterocyclic moiety, as defined above, except that it is attached to the remainder of the molecule via an oxygen atom.
  • Heterocyclic thioether refers to a heterocyclic moiety, as defined above, except that it is attached to the remainder of the molecule via a sulfur atom.
  • Hydroalkyl refers to an -OH appended to an alkyl group, as defined above.
  • Hydroxy-protecting group refers to those groups which are known in the art to protect a hydroxyl group against undesirable reactions during synthetic procedures and to be selectively removable including, but not Umited to, methylthiomethyl, tert- butyldimethylsilyl, tert-butyldiphenylsilyl, acyl substituted with an aryl group, where acyl and aryl are defined above, and the like.
  • Leaving group refers to an alkyl-, alkenyl-, or aryl-substituent, where alkyl, alkenyl, and aryl are as defined above, which in a reaction becomes cleaved to either produce a site of unsaturation or to introduce another substituent.
  • Mod-aryl refers to an aryl group, as defined above, except that the aryl group is unsubstituted or substituted with from one-to-three independently selected substituents, R 302 , rather than R 301 , where R 302 is as defined above.
  • Any two adjacent R 302 substituents in a di- or tri-substituted mod-aryl group may form a 5-, 6- or 7-membered carbocyclic ring or 5-, 6- or 7-membered heterocyclic-ring where the ring atoms are carbon atoms and one or two heteroatoms independently selected from the group consisting of -O-, -S(O) s -, where s is as defined above, and -NR 18 -, where R 18 is as defined above.
  • Mod-Ci-to-Cio-alkyl refers to a -(Ci-to-Cio-alkyl) group substituted with from one-to-six radicals selected from:
  • Mod-C3-to-C ⁇ o-alkenyl refers to a -(C3-to-C ⁇ o-alkenyl) group substituted with from one-to-six radicals selected from:
  • Mod-C 3 -to-C ⁇ o-alkynyl refers to a -(C3-to-C ⁇ o-alkynyl) group substituted with from one-to-six radicals selected from:
  • Mod-cyclo-C3-to-C ⁇ o-alkyl refers to a -(cyclo-C3-to-C ⁇ o-alkyl) group substituted with from one-to-six radicals selected from:
  • Mod-cyclo-C4-to-C ⁇ o-alkenyl refers to a -(cyclo-C4-to-C ⁇ o- alkenyl) group substituted with from one-to-six radicals selected from:
  • Mod-bicyclo-C6-to-C ⁇ o-alkyl refers to a -(bicyclo-C6-to-C ⁇ o-alkyl) group substituted with from one-to-six radicals selected from:
  • Mod-bicyclo-C6-to-C ⁇ o-alkenyl refers to a -(bicyclo-C6-to-C ⁇ o- alkenyl) group substituted with from one-to-six radicals selected from:
  • Mod-Het- refers to a Het group, as defined above, except that the Het group may bear one or more substituents R 302 , rather than R 301 , where R 302 is as defined above or any two adjacent R 302 substituents in a di-, tri-, tetra- or penta-substituted mod-Het group may form a 5-, 6- or 7-membered ring consisting of ring carbon atoms and zero, one or two ring heteroatoms independently selected from the group consisting of -O-, -S(O) s -, where s is as defined above, and -NR 18 -, where R 18 is as defined above.
  • Mod-heterocyclic refers to a heterocycUc group, as defined above, except that the heterocycUc group may bear one or more substituents R 302 , rather than R 301 , where R 302 is as defined above or any two adjacent R 302 substituents in a di-, tri-, tetra- or penta-substituted mod-heterocylic group may form a 5-, 6- or 7-membered ring consisting of carbon atoms and zero, one or two heteroatoms independently selected from the group consisting of -O-, -S(O) s -, where s is as defined above, and -NR 18 -, where R 18 is as defined above.
  • “Monoalkylamino” and “dialkylamino” refer respectively to one and two alkyl groups, as defined above, except that they are appended to the remainder of the molecule via an amino group. Examples include, but are not Umited to, methylamino, isopropylamino, dimethylamino, N,N-methylisopropylamino, and the like.
  • “Monocycloalkylamino” and “dicycloalkylamino” refer respectively to one and two cycloalkyl groups, as defined above, except that they are appended to the remainder of the molecule via an amino group. Examples include, but are not limited to, cyclohexylamino, b._.-(cyclohexyl)amino, and the like.
  • “Mono-halogenated alkyl”, “di-halogenated alkyl” or “tri-halogenated alkyl” refer to alkyl groups, as defined above, of specified and compatible length, respectively substituted with one, two, or three halogen atoms, as defined above.
  • N-alkylcarboxamido refers to an alkylamino group, as defined above, except that it is appended to the remainder of the molecule via a carbonyl group and has the formula HN(alkyl)C(O)-.
  • N-arylcarboxamido refers to an arylamino group, as defined above, except that it is appended to the remainder of the molecule via a carbonyl group and having the formula HN(aryl)C(O)-.
  • “Naturally occuring amino acid” and “standard amino acid” refer to an amino acid selected from the group consisting of alanine, arginine, asparagine, aspartic acid, cysteine, glutamine, glutamic acid, glycine, histidine, isoleucine, leucine, lysine, methionine, phenylalanine, proUne, serine, threonine, tryptophan, tyrosine and valine.
  • N,N-dialkylcarboxamido refers to dialkylamino group, defined above, except that it is appended to the remainder of the molecule via a carbonyl group and has the formula N(alkyl)(alkyl')C(O)-.
  • N-terminal protecting group refers to those groups known in the art to protect the N-terminus against undesirable reactions during synthetic procedures or to prevent the attack of exopeptidases on the final compounds or to increase the solubility of the final compounds and includes, but is not limited to acyl, acetyl, pivaloyl, tert-butylacetyl, tert- butyloxycarbonyl (Boc), benzyloxycarbonyl (Cbz), benzoyl groups, and the like. Other such groups are described by Gross, E. and Meienhofer, J. in The Peptides. Volume 3; Academic Press, 1981. "
  • Oxo refers to an oxygen atom forming a carbonyl group.
  • Per-halogenated alkyl refers to alkyl groups, as defined above, of specified length, substituted with halogen atoms, as defined above, at every available valency.
  • Qualified-aryl refers to substituted and unsubstituted carbocycUc aromatic groups including, but not Umited to, phenyl, 1- or 2-naphthyl, fluorenyl, (1,2)- dihydronaphthyl, (l,2,3 . 4)-tetrahydronaphthyl, indenyl, indanyl and the like, optionally substituted with 1, 2 or 3 substituents independently selected from halo, nitro, cyano, -(Cj-to-Cio-alkyl), alkoxy and halosubstituted alkyl.
  • Qualified-arylalkyl refers to a qualified-aryl group, as previously defined, attached to the remainder of the molecule via an alkyl group.
  • Sub-C ⁇ -to-C ⁇ o-alkyl refers to a -(C ⁇ -to-C ⁇ o-alkyl) substituted with from one-to-six radicals independently selected from the group consisting of:
  • Sub-cyclo-C3-to-C ⁇ o-alkyl refers to a -(cyclo-C3-to-C ⁇ o-alkyl) substituted with from one-to-six radicals independently selected from the group consisting of:
  • Sub-cyclo-C3-to-C ⁇ o-alkyl-C ⁇ -to-C3-alkyl refers to a -(cyclo- C 3 -to-C ⁇ o-alkyl-C ⁇ -to-C3-alkyl) substituted with from one-to-six radicals independently selected from the group consisting of:
  • Sub-C3-to-C ⁇ o-alkenyl refers to a -(C3-to-C ⁇ o-alkenyl) substituted with from one-to-six radicals independently selected from the group consisting of:
  • Sub-cyclo-C4-to-C ⁇ o-alkenyl refers to a -(cyclo- -to-Cio-alkenyl) substituted with from one-to-six radicals independently selected from the group consisting of:
  • Sub-cyclo-C6-to-C ⁇ o-alkyl-C3-C5-alkenyl refers to a -(cyclo- C6-to-C ⁇ o-alkyl-C3-C5-alkenyl) substituted with from one-to-six radicals independently selected from the group consisting of:
  • Sub-C3-to-C ⁇ o-alkynyl refers to a -(C3-to-C ⁇ o-alkynyl) substituted with from one-to-six radicals independently selected from the group consisting of:
  • Sub-cyclo-C6-to-C ⁇ o-alkyl-C3-C5-alkynyl refers to a -(cyclo- C6 ⁇ to-C ⁇ o-alkyl-C 3 -C5-alkynyl) substituted with from one-to-six radicals independently selected from the group consisting of:
  • Sub-bicyclo-C6-to-C ⁇ o-alkyl refers to a -(bicyclo-Cg-to-Cio-alkyl) substituted with from one-to-six radicals independently selected from the group consisting of:
  • Sub-bicyclo-Cg-to-Cio-alkenyl refers to a -(bicyclo-Cg-to- o- alkenyl) substituted with from one-to-six radicals independently selected from the group consisting of:
  • Substituted-bicyclo-C6-to-C ⁇ o-alkyl refers to a -(bicyclo-C6-to-C ⁇ o- alkyl) group substituted with from one-to- three radicals selected from: halogen; -OH; (C ⁇ -C 6 -alkyl)NH-; di(C ⁇ -C 6 -alkyl)N-; -CO 2 H; -CONH 2 ; -SH; (C ⁇ -C6-alkyl)S-; (C ⁇ -C6-alkyl)O-; (C ⁇ -C 6 -alkyl)OC(O)-;mod-aryl-(C ⁇ -C 6 - alkyl)OC(O)-; (C ⁇ -C 6 -alkyl)OC(O)NH-; (C ⁇ -C 6 -alkyl)C(O)NH-; mod-aryl- (C ⁇ -C 6 -a_kyl)OC(O)NH—; halogen;
  • Substituted-C3-to-C6-alkenyl refers to a -(C3-to-C6-alkenyl) group substituted with from one-to-three radicals selected from: halogen; -OH; (C ⁇ -C 6 -alkyl)NH-; di(C ⁇ -C6-alkyl)N-; -CO 2 H; -CONH 2 ; -SH; (C ⁇ -C 6 -alkyl)S-; (C ⁇ -C 6 -alkyl)O-; (C ⁇ -C6-alkyl)OC(O)-;mod-aryl-(C ⁇ -C6- alkyl)OC(O)-; (C ⁇ -C 6 -alkyl)OC(O)NH-; (C ⁇ -C 6 -alkyl)C(O)NH-; mod-aryl- (C ⁇ -C6-alkyl)OC(O)NH-; mod-aryl- (C ⁇ -C6-alkyl
  • Substituted-C ⁇ -to-C6-alkyl refers to a -(Ci-to- -alkyl) group substituted with from one-to-three radicals selected from: halogen; -OH; (C ⁇ -C 6 -alkyl)NH-; di(C ⁇ -C 6 -alkyl)N-; -CO 2 H; -CONH 2 ; -SH; (C ⁇ -C6-alkyl)S-; (C ⁇ -C6-alkyl)O-; (C ⁇ -C6-alkyl)OC(O)-;mod-aryl-(C ⁇ -C 6 - alkyl)OC(O)-; (C ⁇ -C 6 -alkyl)OC(O)NH-; (C ⁇ -C 6 -alkyl)C(O)NH-; mod-aryl- (C ⁇ -C 6 -alkyl)OC(O)NH-; mod-aryl- (C ⁇ -C 6 -alkyl)
  • Substituted-C3-to-C6-alkynyl refers to a -(C3-to-C6-alkynyl) group substituted with from one-to-three radicals selected from: halogen; -OH; (C ⁇ - -alkyl)NH-; di(C ⁇ -C 6 -alkyl)N-; -CO 2 H; -CONH 2 ; -SH; (C ⁇ -C 6 -alkyl)S-; (C ⁇ -C 6 -alkyl)O-; (C ⁇ -C 6 -alkyl)OC(O)-;mod-aryl-(C ⁇ -C 6 - alkyl)OC(O)-; (C ⁇ -C 6 -alkyl)OC(O)NH-; (C ⁇ -C 6 -alkyl)C(O)NH-; mod-aryl- (C ⁇ -C 6 -alkyl)OC(O)NH-; mod-aryl- (C ⁇ -C 6
  • Substituted-cyclo-C4-to-C ⁇ o-alkenyl refers to a -(cyclo-C4-to-C ⁇ o- alkenyl) group substituted with from one-to-three radicals selected from: halogen; -OH; (C ⁇ -C 6 -alkyl)NH-; di(C ⁇ -C6-alkyl)N-; -CO 2 H; -CONH 2 ; -SH; (C ⁇ -C6-alkyl)S-; (C ⁇ -C6-alkyl)O-; (C ⁇ -C 6 -alkyl)OC(O)-;mod-aryl-(C ⁇ -C 6 - alkyl)OC(O)-; (C ⁇ -C 6 -alkyl)OC(O)NH-; (C ⁇ -C 6 -alkyl)C(O)NH-; mod-aryl- (C ⁇ -C 6 -alkyl)OC(O)NH-;
  • Substituted-cyclo-C3-to-C ⁇ o-alkyl refers to a -(cyclo-C3-to-C ⁇ o- alkyl) group substituted with from one-to-three radicals selected from: halogen; -OH; (C ⁇ -C 6 -alkyl)NH-; di(C ⁇ -C6-alkyl)N-; -CO 2 H; -CONH 2 ; -SH;
  • Substituted-bicyclo-C6-to-C ⁇ o-alkenyl-C ⁇ -to-C6-alkyl refers to a -(bicyclo-C6-to-C ⁇ o-alkenyl)-C ⁇ -to-C6-alkyl group substituted with from one-to-three radicals selected from: halogen; -OH; (C ⁇ -C 6 -alkyl)NH-; di(C ⁇ -C6-alkyl)N-; -CO 2 H; -CONH 2 ; -SH; (C ⁇ -C 6 -alkyl)S-; (C ⁇ -C 6 -alkyl)O-; (C ⁇ -C 6 -alkyl)OC(O)-;mod-aryl-(C ⁇ -C 6 - alkyl)OC(O)-; (C ⁇ -C 6 -alkyl)OC(O)NH-; (C ⁇ -C 6 -alkyl)C(O
  • “Thiolalkyl” refers to an alkyl group, as defined above, substituted with an -SH group.
  • Thiooxo refers to a sulfur atom forming a thiocarbonyl group.
  • Unsubstituted aryl refers to mono-, di-, tri- or tetracyclic aromatic groups, charged or uncharged, the rings of which are comprised of from 3-to-7 carbon atoms. Examples of unsubstituted aryl include, but are not Umited to, phenyl, 1- or 2-naphthyl, azulenyl, fluorenyl, (1, 2)-dihydronaphthyl, (l,2,3 . 4)-tetrahydronaphthyl, indenyl, indanyl and the like, which are solely substituted by hydrogen.
  • “Pharmaceutically-acceptable salts, esters, amides and prodrugs” refers to those carboxylate salts, amino acid addition salts, esters, amides and prodrugs of the compounds of the present invention which are, within the scope of sound medical judgement, suitable for use in contact with the tissues of humans and lower animals without undue toxicity, irritation, allergic response, or the like, commensurate with a reasonable benefit/risk ratio, and effective for their intended use, as well as the zwitterionic forms, where possible, of the compounds of the invention.
  • salts refers to the relatively non-toxic, inorganic and organic acid addition salts of compounds of the present invention, which may be prepared in situ during the final isolation and purification of the compounds or by separately reacting the purified compound in its free base form with a suitable organic or inorganic acid and isolating the salt thus formed.
  • Representative salts include the hydrobromide, hydrochloride, sulfate, bisulfate, phosphate, nitrate, acetate, oxalate, valerate, oleate, palmitate, stearate, laurate, borate, benzoate, lactate, phosphate, tosylate, citrate, maleate, fumarate, succinate, tartrate, naphthylate, mesylate, glucoheptonate, lactiobionate and laurylsulphonate salts and the like.
  • alkali and alkaline earth metals such as sodium, lithium, potassium, calcium, magnesium and the like
  • nontoxic ammonium, quaternary ammonium and amine cations including, but not limited to, ammonium, tetramethylammonium, tetraethylammonium, methylamine, dimethylamine, trimethylamine, triethylamine, ethylamine, and the like (see, for example S. M. Berge, et al., "Pharmaceutical Salts.” J. Pharm. Sci. 66: 1-19 (1977)).
  • esters of the compounds of this invention examples include C ⁇ -to-C6-alkyl esters wherein the alkyl group is a straight or branched chain. Acceptable esters also include Cs-to-C ⁇ -cycloalkyl esters as well as arylalkyl esters such as, but not Umited to benzyl. C ⁇ -to-C4 alkyl esters are prefe ⁇ ed. Esters of the compounds of the present invention may be prepared according to conventional methods.
  • non-toxic esters of alcoholic moieties on the compounds of the invention may be constructed by condensing these alcohols with C ⁇ -to-C6-alkyl carboxylic acids, C ⁇ -to-C6- alkyl dicarboxylic acids or aryl-carboxylic acids.
  • esters include, but are not limited to acetyl, benzoyl or hemi-succinyl.
  • Examples of pharmaceutically-acceptable, non-toxic amides of the compounds of this invention include amides derived from ammonia, primary C ⁇ -to-C6- alkyl amines and secondary di-C ⁇ -to-C6-alkyl amines. In the case of secondary amines the amine may also be in the form of a 5-or- 6 membered heterocycle containing one nitrogen atom. Amides derived from ammonia, C ⁇ -to-C3-alkyl primary amides and di-C ⁇ -to-C 2 -alkyl secondary amides are prefe ⁇ ed. Amides of the compounds of the invention may be prepared according to conventional methods.
  • Prodrug refers to compounds that are rapidly transformed in vivo to yield the parent compound of the above formula, for example, by hydrolysis in blood.
  • a thorough discussion is provided in T. Higuchi and V. Stella, "Pro-drugs as Novel DeUvery Systems", Vol 14 of the A.C.S. Symposium Series, and in Bioreversible Carriers in Drug Design, ed. Edward B. Roche, American Pharmaceutical Association and Pergamon Press, 1987.
  • Prodrugs of compounds of the present invention may be prepared by suitable methods.
  • the condensation of the drug's amino group with amino acids and peptides may be effected in accordance with conventional condensation methods such as the azide method, the mixed acid anhydride method, the DCC (dicyclohexylcarbodiimide) method, the active ester method (p-nitrophenyl ester method, N-hydroxysuccinic acid imide ester method, cyanomethyl ester method and the like), the Woodward reagent K method, the DCC-HOBT (1 -hydroxy- benzotriazole) method and the like.
  • Classical methods for amino acid condensation reactions are described in "Peptide Synthesis” Second Edition, M. Bodansky, Y.S. Klausner and M.A. Ondetti (1976).
  • branched chain amino and carboxyl groups at alpha and omega positions in amino acids may be protected and deprotected if necessary.
  • the protecting groups for amino groups which can be used involve, for example, benzyloxycarbonyl (Z or Cbz), o-chlorobenzyloxycarbonyl ((2-Cl)Z)), p- nitrobenzyloxycarbonyl (Z(NO2)), p-methoxybenzyloxycarbonyl (Z(OMe)), t- amyloxycarbonyl (Aoc), isobornealoxycarbonyl, adamantyloxycarbonyl (Adoc), 2-(4- biphenyl)-2-propyloxy carbonyl (Bpoc), 9-fluorenyl-methoxycarbonyl (Fmoc), methylsulfonylethoxy carbonyl (Msc), trifluoroacetyl, phthalyl, formyl, 2- nitrophenylsulf
  • protecting groups for carboxyl groups involve, for example, benzyl ester (OBzl), cyclohexyl ester, 4-nitrobenzyl ester (OBzlNO2), t-butyl ester (OtBu), 4- pyridylmethyl ester (OPic), and the like.
  • the guanidino group (NG) in arginine may be protected with nitro, p-toluenesulfonyl (Tos), benzyloxycarbonyl (Z), adamantyloxycarbonyl (Adoc), p-methoxybenzenesulfonyl, 4-methoxy-2,6-dimethyl- benzenesulfonyl (Mts) and the like;
  • the thiol group in cysteine may be protected with benzyl, p-methoxybenzyl, triphenylmethyl, acetamidomethyl, ethylcarbamyl, 4-methylbenzyl (4-MeBzl), 2,4,6-trimethylbenzyl (Tmb) and the like; and the hydroxy group in serine may be protected with benzyl (Bzl), t-butyl, acetyl, tetrahydropyranyl (THP), and the like
  • potent immunomodulatory activity which compounds of the instant invention demonstrate, in common in vitro biological assays, indicate that these compounds possess immunosuppressive, antimicrobial, antifungal, antiviral, antunflammatory, and antiproliferative activity, and possess the abiUty to reverse chemotherapeutic drug resistance.
  • the compounds are useful as prophylactics for the prevention of HIV replication.
  • the compounds of the present invention are useful when administered for the prevention immune-mediated tissue or organ graft rejection.
  • transplanted tissues and organs which suffer from these effects are heart, kidney, liver, . medulla ossium, skin, cornea, lung, pancreas, intestinum ***, limb, muscle, nervus, duodenum, small-bowel, pancreatic-islet-cell, and the like; as well as graft-versus-host diseases brought about by meduUa ossium transplantation.
  • the regulation of the immune response by the compounds of the invention would also find utility in the treatment of autoimmune diseases, such as rheumatoid arthritis, systemic lupus erythematosus, Hashimoto's thyroiditis, multiple sclerosis, myasthenia gravis, type I diabetes, uveitis, allergic encephalomyeutis, glomerulonephritis, and the like; and further infectious diseases caused by pathogenic microorganisms, such as HIV.
  • autoimmune diseases such as rheumatoid arthritis, systemic lupus erythematosus, Hashimoto's thyroiditis, multiple sclerosis, myasthenia gravis, type I diabetes, uveitis, allergic encephalomyeutis, glomerulonephritis, and the like
  • infectious diseases caused by pathogenic microorganisms, such as HIV.
  • pathogenic microorganisms such as HIV.
  • inhibition of T-cell mitosis would suppress
  • Further uses include the treatment and prophylaxis of inflammatory and hyperproliferative skin diseases and cutaneous manifestations of immunologically-mediated illnesses, such as psoriasis, atopical dermatitis, contact dermatitis and further eczematous dermatitises, sebo ⁇ hoeis dermatitis, Lichen planus, Pemphigus, bullous pemphigoid, Epidermolysis bullosa, urticaria, angioedemas, vasculitides, erythemas, cutaneous eosinophilias, Lupus erythematosus, acne, diseases or syndromes resulting in hair loss including but not limited to Alopecia areata.
  • immunologically-mediated illnesses such as psoriasis, atopical dermatitis, contact dermatitis and further eczematous dermatitises, sebo ⁇ hoeis dermatitis, Lichen planus, Pemphigus, bullous
  • a compound of the invention would be useful include various eye diseases (autoimmune and otherwise) such as keratoconjunctivitis, vernal conjunctivitis, keratitis, herpetic keratitis, conical cornea, dystrophia epithelialis comeae, corneal leukoma, ocular pemphigus, Mooren's ulcer, Scleritis, Graves' opthalmopathy, Vogt-Koyanagi-Harada syndrome, sarcoidosis, etc.; reversible obstructive airway disease, which includes conditions such as asthma (for example, bronchial asthma, aUergic asthma, intrinsic asthma, extrinsic asthma and dust asthma), particularly chronic or inveterate asthma (for example, late asthma and airway hyper-responsiveness), bronchitis and the like; inflammation of mucosa and blood vessels such as gastric ulcers, vascular damage caused by ischemic diseases and thrombosis.
  • hyperproU stea
  • Other treatable conditions would include but are not Umited to ischemic bowel diseases, inflammatory bowel diseases, necrotizing enterocolitis, intestinal lesions associated with thermal burns and leukotriene B4-mediated diseases; intestinal inflammations/allergies such as Coeliac diseases, proctitis, eosinophilic gastroenteritis, mastocytosis, Crohn's disease and ulcerative coUtis; food-related aUergic diseases which have symptomatic manifestation remote from the gastro-intestinal tract (e.g., migraine, rhinitis and eczema); renal diseases such as ' interstitial nephritis, Goodpasture's syndrome, hemolytic-uremic syndrome and diabetic nephropathy; nervous diseases such as multiple myositis, Guillain-Barre syndrome, Meniere's disease, polyneuritis, multiple neuritis, mononeuritis and radiculopathy; endocrine diseases such as hyperthyroidism and Basedow's disease; he
  • the compounds of the invention are useful for the treatment and prevention of hepatic disease such as immunogenic diseases (for example, chronic autoimmune liver diseases such as the group consisting of autoimmune hepatitis, primary biliary ci ⁇ hosis and sclerosing cholangitis), partial liver resection, acute liver necrosis (e.g., necrosis caused by toxin, viral hepatitis, shock or anoxia), B-virus hepatitis, non-A/non-B hepatitis, cirrhosis (such as alcoholic ci ⁇ hosis) and hepatic failure such as fulminant hepatic failure, late-onset hepatic failure and "acute-on-chronic" liver failure (acute Uver failure on chronic liver diseases), and moreover are useful for various diseases because of their useful activity such as augmention of chemotherapeutic effect, preventing or treating activity of cytomegalovirus infection, particularly HCMV infection, anti-inflammatory activity, and so on.
  • some compounds also possess FK-506 antagonistic properties, and are thus useful in the treatment of immunodepression or a disorder involving immunodepression.
  • disorders involving immunodepression include AIDS, cancer, senile dementia, trauma (including wound heaUng, surgery and shock), chronic bacterial infection, and certain central nervous system disorders.
  • the immunodepression to be treated may be caused by an overdose of an immunosuppressive macrocyclic compound, for example derivatives of 12- (2-cyclohexyl-l-methylvinyl)-13, 19,21,27-tetramethyl-l l,28-dioxa-4-azatricyclo[22.3.1.0 4 ' 9 ] octacos-18-ene such as FK-506, or rapamycin. Overdosing of such medicants by patients is quite common upon their reaUzing that they have forgotten to take their medication at the prescribed time and can lead to serious side effects.
  • a further situation in which the compounds of the present invention may be used to treat immunosuppression is in vaccination. It is sometimes found that the antigen introduced into the body for the acquisition of immunity from disease also acts as an immunosuppressive agent, and therefore antibodies are not produced by the body and immunity is not acquired. By introducing a compound of the present invention into the body (as in a vaccine), the undesired immunosuppression may be overcome and immunity acquired.
  • the compounds of the present invention may also find utility in the chemosensitization of drug resistant target cells.
  • Cyclosporin A and FK-506 are known to be effective modulators of P-glycoprotein, a substance which binds to and inhibits the action of anticancer drugs; by inhibiting P-glycoprotein, they are capable of increasing the sensitivity of multidrug resistant (MDR) ceUs to chemotherapeutic agents.
  • MDR multidrug resistant
  • the compounds of the invention may likewise be effective at overcoming resistance expressed to clinically useful antitumour drugs such as 5-fluorouracil, cisplatin, methotrexat ⁇ , vincristine, vinblastine and adriamycin, colchicine and vincristine.
  • the steroid receptor-associated heat shock proteins hsp56 or hsp59, belong to the FK506 family of immunophiUn proteins.
  • the ability of a steroid receptor-associated heat shock protein to bind the immunosuppressive macrolide FK506 may suggest that the steroid receptor and immunophi n signal transduction pathways are functionally interrelated.
  • the combined treatment of compounds of the present invention and low concentrations of a steroid Ugand eg. progesterone, dexamethasone
  • the compounds of the present invention may potentiate steroid-mediated transactivation.
  • Aqueous liquid compositions of the present invention may be particularly useful for the treatment and prevention of various diseases of the eye such as autoimmune diseases (including, for example, conical cornea, keratitis, dysophia epithelialis corneae, leukoma, Mooren's ulcer, sclevitis and Graves' ophthalmopathy) and rejection of corneal transplantation.
  • autoimmune diseases including, for example, conical cornea, keratitis, dysophia epithelialis corneae, leukoma, Mooren's ulcer, sclevitis and Graves' ophthalmopathy
  • a therapeutically-effective amount of one of the compounds of the present invention meaning a sufficient amount of the compound to treat a particular disorder, at a reasonable benefit risk ratio, may be employed in pure form or, where such forms exist, in pharmaceutically acceptable salt, ester or prodrug form.
  • the compound may be administered as pharmaceutical compositions containing the compound of interest in combination with one or more pharmaceuticaUy - acceptable excipients. It will be understood, however, that the total daily usage of the compounds and compositions of the present invention will be decided by the attending physician within the scope of sound medical judgement.
  • the specific therapeuticaUy-effective dose level for any particular patient wUl depend upon a variety of factors including the disorder being treated and the severity of the disorder; activity of the specific compound employed; the specific composition employed; the age, body weight, general health, sex and diet of the patient; the time of administration, route of administration, and rate of excretion of the specific compound employed; the duration of the treatment; drugs used in combination or coincidental with the specific compound employed; and like factors well known in the medical arts. For example, it is well within the skill of the art to start doses of the compound at levels lower than required to achieve the desired therapeutic effect and to gradually increase the dosage until the desired effect is achieved.
  • the total daily dose of the compounds of this invention administered to a human or lower animal may range from about 0.001 to about 10 mg/kg of patients body mass/day.
  • more preferable doses may be in the range of from about 0.005 to about 3 mg/kg/day.
  • the effective daily dose may be divided into multiple doses for purposes of administration; consequently, single dose compositions may contain such amounts or submultiples thereof to make up the daily dose.
  • compositions of the present invention comprise a compound of the invention and a pharmaceutically-acceptable earner or excipient, meaning a non-toxic solid, semi-solid or liquid filler, diluent, encapsulating material or formulation auxiliary of any type, which may be administered orally, rectally, parenterally, intracisternally, intravaginally, intraperitoneally, topically (as by powders, ointments, drops or transdermal patch), bucally, or as an oral or nasal spray.
  • parenteral refers to modes of administration which include intravenous, intramuscular, intraperitoneal, intrasternal, subcutaneous and intraarticular injection and infusion.
  • compositions of this invention for parenteral injection comprise pharmaceuticaUy-acceptable sterile aqueous or nonaqueous solutions, dispersions, suspensions or emulsions, as weU as sterile powders for reconstitution into sterile injectable solutions or dispersions just prior to use.
  • suitable aqueous and nonaqueous earners, diluents, solvents or vehicles include water, ethanol, polyols (such as glycerol, propylene glycol, polyethylene glycol, and the like), carboxymethylceUulose and suitable mixtures thereof, vegetable oils (such as olive oil), and injectable organic esters such as ethyl oleate.
  • Proper fluidity may be maintained, for example, by the use of coating materials such as lecithin, by the maintenance of the required particle size in the case of dispersions, and by the use of surfactants.
  • compositions may also contain adjuvants such as preservative, wetting agents, emulsifying agents, and dispersing agents. Prevention of the action of microorganisms may be ensured by the inclusion of various antibacterial and antifungal agents, for example, paraben, chlorobutanol, phenol sorbic acid, and the like. It may also be desirable to include isotonic agents such as sugars, sodium chloride, and the like, Prolonged absorption of the injectable pharmaceutical form may be brought about by the inclusion of agents which delay absorption, such as aluminum monostearate and gelatin.
  • adjuvants such as preservative, wetting agents, emulsifying agents, and dispersing agents.
  • the absorption of the drug in order to prolong the effect of the drug, it is desirable to slow the absorption of the drug from subcutaneous or intramuscular injection. This may be accomplished by the use of a Uquid suspension of crystalline or amorphous material with poor water solubility. The rate of absorption of the drug then depends upon its rate of dissolution which, in turn, may depend upon crystal size and crystalline form. Alternatively, delayed absorption of a parenterally administered drug form is accomplished by dissolving or suspending the drug in an oil vehicle.
  • Injectable depot forms are made by forming microencapsule matrices of the drug in biodegradable polymers such as polylactide-polyglycolide, poly(orthoesters) and poly(anhydrides). Depending upon the ratio of drug to polymer and the nature of the particular polymer employed, the rate of drug release can be controUed. Depot injectable formulations are also prepared by entrapping the drug in liposomes or microemulsions which are compatible with body tissues.
  • the injectable formulations may be steriUzed, for example, by filtration through a bacterial-retaining filter, or by incorporating sterilizing agents in the form of sterile soUd compositions which can be dissolved or dispersed in sterile water or other sterile injectable medium just prior to use.
  • Solid dosage forms for oral administration include capsules, tablets, piUs, powders, and granules.
  • the active compound is mixed with at least one inert, pharmaceutically-acceptable excipient or earner, such as sodium citrate or dicalcium phosphate and/or a) fiUers or extenders such as starches, lactose, sucrose, glucose, mannitol, and siUcic acid, b) binders such as, for example, carboxymethylceUulose, alginates, gelatin, polyvinylpyrrolidone, sucrose, and acacia, c) humectants such as glycerol, d) disintegrating agents such as agar-agar, calcium carbonate, potato or tapioca starch, alginic acid, certain sUicates, and sodium carbonate, e) solution retarding agents such as paraffin, f) absorption accelerators such as quaternary ammonium compounds, g) wetting agents such as
  • compositions of a similar type may also be employed as fillers in soft and hard- fiUed gelatin capsules using such excipients as lactose or milk sugar as well as high molecular weight polyethylene glycols and the like.
  • the solid dosage forms of tablets, dragees, capsules, pills, and granules may be prepared with coatings and shells such as enteric coatings and other coatings well known in the pharmaceutical formulating art. They may optionally contain opacifying agents and can also be of a composition that they release the active ingredient(s) only, or preferentially, in a certain part of the intestinal tract, optionally, in a delayed manner. Examples of embedding compositions which can be used include polymeric substances and waxes.
  • the active compounds can also be in micro-encapsulated form, if appropriate, with one or more of the above-mentioned excipients.
  • Liquid dosage forms for oral administration include pharmaceutically-acceptable emulsions, solutions, suspensions, syrups and elixirs.
  • the Uquid dosage forms may contain inert diluents commonly used in the art such as, for example, water or other solvents, solubiUzing agents and emulsifiers such as ethyl alcohol, isopropyl alcohol, ethyl carbonate, ethyl acetate, benzyl alcohol, benzyl benzoate, propylene glycol, 1,3-butylene glycol, dimethyl formamide, oUs (in particular, cottonseed, groundnut, corn, germ, oUve, castor, and sesame oUs), glycerol, tetrahydrofurfuryl alcohol, polyethylene glycols and fatty acid esters of sorbitan, and mixtures thereof.
  • inert diluents commonly used in the art such as, for example, water or other solvents,
  • the oral compositions can also include adjuvants such as wetting agents, emulsifying and suspending agents, sweetening, flavoring, and perfuming agents.
  • adjuvants such as wetting agents, emulsifying and suspending agents, sweetening, flavoring, and perfuming agents.
  • Suspensions may contain, in addition to the active compounds, suspending agents as, for example, ethoxylated isostearyl alcohols, polyoxyethylene sorbitol and sorbitan esters, microcrystalline cellulose, aluminum metahydroxide, bentonite, agar-agar, and tragacanth, and mixtures thereof.
  • Topical administration includes administration to the skin or mucosa, including surfaces of the lung and eye.
  • Compositions for topical administration, including those for inhalation, may be prepared as a dry powder which may be pressurized or non-pressurized.
  • the active ingredient in finely divided form may be used in admixture with a larger-sized pharmaceutically-acceptable inert carrier comprising particles having a size, for example, of up to 100 micrometers in diameter.
  • Suitable inert earners include sugars such as lactose.
  • at least 95% by weight of the particles of the active ingredient have an effective particle size in the range of 0.01 to 10 micrometers.
  • the composition may be pressurized and contain a compressed gas, such as nitrogen or a liquified gas propeUant.
  • a compressed gas such as nitrogen or a liquified gas propeUant.
  • the Uquified propeUant medium and indeed the total composition is preferably such that the active ingredient does not dissolve therein to any substantial extent.
  • the pressurized composition may also contain a surface active agent, such as a Uquid or soUd non-ionic surface active agent or may be a solid anionic surface active agent. It is prefe ⁇ ed to use the solid anionic surface active agent in the form of a sodium salt.
  • a further form of topical administration is to the eye, as for the treatment of immune- mediated conditions of the eye such as automimmue diseases, allergic or inflammatory conditions, and corneal transplants.
  • the compound of the invention is deUvered in a pharmaceuticaUy acceptable ophthalmic vehicle, such that the compound is maintained in contact with the ocular surface for a sufficient time period to allow the compound to penetrate the corneal and internal regions of the eye, as for example the anterior chamber, posterior chamber, vitreous body, aqueous humor, vitreous humor, cornea, iris/diary, lens, choroid/retina and sclera.
  • the pharmaceuticaUy-acceptable ophthalmic vehicle may, for example, be an ointment, vegetable oil or an encapsulating material.
  • compositions for rectal or vaginal administration are preferably suppositories which may be prepared by mixing the compounds of this invention with suitable non-irritating excipients or earners such as cocoa butter, polyethylene glycol or a suppository wax which are solid at room temperature but Uquid at body temperature and therefore melt in the rectum or vaginal cavity and release the active compound.
  • suitable non-irritating excipients or earners such as cocoa butter, polyethylene glycol or a suppository wax which are solid at room temperature but Uquid at body temperature and therefore melt in the rectum or vaginal cavity and release the active compound.
  • Liposomes are generally derived from phosphoUpids or other lipid substances. Liposomes are formed by mono- or multi-lamellar hydrated Uquid crystals that are dispersed in an aqueous medium. Any non-toxic, physiologically-acceptable and metaboUzable lipid capable of forming liposomes can be used.
  • the present compositions in liposome form can contain, in addition to a compound of the present invention, stabiUzers, preservatives, excipients, and the like.
  • the prefe ⁇ ed lipids are the phosphoUpids and the phosphatidyl cholines (lecithins), both natural and synthetic. Methods to form liposomes are known in the art. See, for example, Prescott, Ed., Methods in Cell Biology, Volume XIV, Academic Press, New York, N.Y. (1976), p. 33 et seq.
  • the compounds of the invention may be prepared using one or more processes.
  • the starting materials for use in these processes are preferably one of the macrolides isolated from culture media obtained in accordance with known methods by fermentation of microorganisms of the genus Streptomyces, which are disclosed in European Patent Application No. 0184162.
  • Samples are avaUable from the Fermentation Research Institute, Tsukuba, Ibaraki 305, Japan under the provisions of the Budapest Treaty, under deposit No. FERM BP-927. This strain has been redeposited on April 27, 1989 with the Agricultural Research Culture CoUection Intemational Depository, Peoria, Illinois 61604, USA under the provisions of the Budapest Treaty, under deposit No. NRRL 18488.
  • the macrolide FR- 900520 (European Patent Application 0184162), also known as ascomycin, may be prepared in accordance to the published methods of (i) H. Hatanaka, M. Iwami, T. Kino, T. Goto and M. Okuhara, FR-900520 and FR-900523, Novel immunosuppressants isolated from A streptomyces. I. Taxonomy of the producing strain. J . Antibiot., 1988. XLI(ll), 1586-1591; (ii) H. Hatanaka, T. Kino, S. Miyata, N. Inamura, A. Kuroda, T. Goto, H. Tanaka and M.
  • Such processes comprise:
  • suitable reagents for activation of an alcohol include acetic anhydride, trifluoromethanesulfonic anhydride (triflic anhydride), methanesulfonyl chloride (mesyl chloride), /.-toluenesulfonyl chloride (tosyl chloride), trifluoroacetic anhydride, trifluoroacetyl chloride, methoxysulfonyl fluoride (magic methyl), o-nitrobenzenesulfonyl chloride, l-methyl-2-fluoropyridinium salt and the like.
  • the activation may be carried out in a solvent which does not adversely affect the reaction (e.g., diethylether, dichloromethane, tetrahydrofuran, chloroform or NN- dimethylformamide or a mixture thereof).
  • the reaction may require cooling or heating, depending on the activation method chosen.
  • the reaction is preferably conducted in the presence of an organic or inorganic base such as an alkaUne earth metal (e.g. calcium, etc.), alkali metal hydride (e.g. sodium hydride, etc.), alkaU metal hydroxide (e.g. sodium hydroxide, potassium hydroxide, etc.), alkaU metal carbonate (e.g.
  • alkaU metal hydrogen carbonate e.g. sodium hydrogen carbonate, potassium hydrogen carbonate, etc.
  • alkaU metal alkoxide e.g. sodium methoxide, sodium ethoxide, potassium tert-butoxide, etc.
  • alkali metal alkanoic acid e.g. sodium acetate, etc.
  • tiialkylamine e.g. triethylamine, etc.
  • pyridine compounds e.g. pyridine, lutidine, picoline, 4-N,N-dimethylaminopyridine, etc.
  • quinoline preferably in the presence of organic bases such as triethylamine or pyridine.
  • the activation may also be ca ⁇ ied out using a starting material having an opposite configuration at a carbon center.
  • the following two additional steps are required to yield a starting material having an epimeric hydroxyl moiety, i.e. (1) the alcohol is oxidized to its co ⁇ esponding ketone, (2) the obtained ketone is reduced under selective conditions.
  • Both chiral centers having either [Rj- or [S] -configuration can be obtained selectively and separately.
  • suitable azide reagents include well-estabUshed alkali metal azides such as sodium or Uthium azides (NaN3 or L1N3) in the presence or absence of crown ethers, more reactive tetraalkylammonium azides (Danishefski, S. J.; DeNinno, M. P.; Chen, S.-H. J. Am. Chem. Soc. 1988, 110, 3929), tetramethylguanidinium azide, (Papa, A. J. J. Org. Chem. 1966, 31, 1426), a copper-assisted azide reaction (Yamamoto, Y.; Asao, N. /. Org. Chem.
  • the azide displacement reaction may be ca ⁇ ied out in a solvent which does not adversely affect the reaction (e.g. chloroform, dichloromethane, tetrahydrofuran, pyridine, dimethylsulfoxide, NN-dimethylformamide, hexamethylphosphoramide, etc. or a mixture thereof).
  • the reaction may be conducted above, at, or below ambient temperature.
  • the reduction may be carried out catalytically using hydrogen.
  • Suitable catalysts include, but are not limited to platinum catalysts (e.g. platinum oxide, platinum black), palladium catalysts (e.g. palladium oxide, paUadium on charcoal, palladium black, palladium hydroxide on charcoal, palladium on calcium carbonate poisoned with lead, palladium on barium carbonate with quinoline), nickel catalysts (e.g. nickel oxide, Raney nickel), rhodium catalysts (e.g. rhodium on alumina). Reduction may also be carried out using metal reducing reagents (see Review; Scriven, E. F. V.; Turnbull, K. Chem Rev.
  • the reduction may be carried out in a solvent which does not adversely affect the reaction (e.g., alcohols, water, acetone, dichloromethane, tetrahydrofuran, pyridine or NN- dimethylformamide or a mixture thereof).
  • a solvent which does not adversely affect the reaction
  • the reaction may be conducted above, at, or below ambient temperature.
  • suitable N-acylations may be carried out using the methods of symmetric carboxylic acid anhydrides, carboxylic acid halides, mixed carbonic-carboxylic anhydrides, active esters (p-nitrophenylester, trichlorophenyl ester, pentafluorophenyl ester, N-hydroxysuccinimide, cyanoethyl, 2,2,2-trichloroethyl and the like), and carboxylic acid with suitable condensing reagents such as DCC (N,N-dicyclohexylcarbodiimide and its related condensing agents), DCC-HOBt (NN-dicyclohexylcarbodiimide-1- hydroxybenzotriazole), Woodward reagent K method, NJV-carbonyldiimidazole and phosphonium containing reagents (e.g.
  • Suitable reagents for amide formation include, but are not limited to formyl derivatives, acetyl halides (chloroacetyl, trichloroacetyl, ⁇ -nitrophenylacetyl, o-nitrophenoxyacetyl, acetoacetyl, [N'-dithiobenzyloxycarbonylaminojacetyl and the like), and substituted propionyl derivatives (3-phenylpropionyl, isobutyryl, picoUnoyl, and the like).
  • Other groups may be found in volume 3 of The Peptides Gross, E. and Meinhofer, J. Academic Press, 1981 and Protective Groups in Organic Synthesis Greene, T. W.
  • the N-acylation may be carried out in a solvent which does not adversely affect the reaction (e.g. acetone, dichloromethane, chloroform, tetrahydrofuran, NN-dimethylformamide, dimethylsulf oxide, diethylether, and the like, or a mixture thereof).
  • a solvent which does not adversely affect the reaction (e.g. acetone, dichloromethane, chloroform, tetrahydrofuran, NN-dimethylformamide, dimethylsulf oxide, diethylether, and the like, or a mixture thereof).
  • the reaction may be conducted above, at, or below ambient temperature.
  • metal salts may be formed from the desired amines and then condensed with an ester which may or may not be activated.
  • salts may be formed by treatment of the neutral amine with trialkylaluminums (See J. I. Levin, E. Turos, S. M. Weinreb Synthetic Communications 1982, 12, 989-93), Sn[ ⁇ (Si(CH 3 ) 3 )] 2 (See W. Wang, E. J. Roskamp /. Org. Chem. 1992, 57, 6101-3), or grignard reagents. For other methods see A. SoUadie-Cavallo, M. Bencheqroun J. Org. Chem. 1992, 57, 5831-4 as well as footnotes 2, 3, 4, 5, 6 and 7 therein.
  • N-alkylations may be carried out using aldehydes or ketones-foUowed by reduction of the initiaUy formed iminium ion ⁇
  • the following reagents can be used for the reduction; sodium cyanoborohydride-boron trifluoride or the reducing reagents cited in process (c) ⁇ , co ⁇ esponding halides in the presence of bases Usted in process (a), or lithium dialkyl cuprate (King, F. E.; King, T. J.; Muir, I. H. M. J. Chem. Soc. 1946, 5; Yamamoto, H.; Maruoka, K. J. Org. Chem. 1980, 45, 2739).
  • Suitable reagents for N-alkylation include, but are not Umited to benzyl halide, 3,4-dimethoxybenzyl haUde, nitrobenzyl halide, di(p- methoxyphenyl)methyl halide, triphenylmethyl halide, and the like.
  • Other groups may be found in volume 3 of The Peptides, Gross, E. and Meinhofer, J. Academic Press, 1981 and Protective Groups in Organic Synthesis, Greene, T. W. John Wiley & Sons, New York, Chapter 7, 1981.
  • the N-alkylation may be ca ⁇ ied out in a solvent which does not adversely affect the reaction (e.g., acetone, dichloromethane, tetrahydrofuran, pyridine or NN- dimethylformamide or a mixture thereof).
  • the reaction may be conducted above, at, or below ambient temperature.
  • urea formation may be ca ⁇ ied out from the following reactions; reaction with silicon tetraisocyanate or sUicon tetraisothiocyanate (NeviUe, R. G.; McGee, J. J. Can. J. Chem.
  • reaction with NN-carbonyldiimidazole or NN- thiocarbonyldiimidazole foUowed by N-substituted primary or secondary amines or ammonia (Staab, H. A.; Wendel, K. Org. Synth. 1968, 48, 44), and reaction with phosgene or thiophosgene in the presence of tert-amine, followed by N-substituted primary or secondary amines or ammonia.
  • the ureido formation may be carried out in a solvent which does not adversely affect the reaction (e.g. acetone, toluene, dichloromethane, tetrahydrofuran, pyridine, NN-dimethylformamide, etc. or a mixture thereof).
  • the reaction may be conducted above, at, or below ambient temperature.
  • urea formation may be ca ⁇ ied out by first forming an acyl azide by activating a carboxyUc acid in the molecule with a chloroformate, such as isobutyl chloroformate, in the presence of a tertiary amine, such as ⁇ -methyl-morpholine or ⁇ - methyl-piperidine, and treating with an azide source, such as sodium azide, hydrazoic acid, trimethylsilylazide, or tetramethylguanidinium azide.
  • the acyl azide may also be formed directly using diphenylphophorylazide in the presence of a tertiary amine.
  • the reaction mixture is then heated at from 40 °C to 100 °C for 0.5 to 6 hours, whereupon the amine H ⁇ R 14 R 15 is added at a temperature at from 23 °C to 100 °C.
  • the reaction is conducted in an inert organic solvent such as diethyl ether, tetrahydrofuran, 1,4-dioxane, chloroform, methylene chloride, benzene, or toluene.
  • N-sulfonylation may be ca ⁇ ied out using substituted sulfonylhaUdes in the presence of suitable tert-amines such as tiialkylamine, pyridine, and the like (Remers, W. A.; Roth, R. H.; Gibs, G. J.; Weiss, M. J. J. Org. Chem. 1971, 36, 1232).
  • suitable tert-amines such as tiialkylamine, pyridine, and the like
  • Suitable reagents include, but are not Umited to benzenesulf onyl haUde, p-methyoxybenzenesulf onyl haUde, 2,4,6-trimethylbenzenesulf onyl haUde, toluenesulfonyl haUde, benzylsulf onyl halide, p- methoxybenzylsulfonyl haUde, trifluoromethylsulfonyl haUde, phenacylsulfonyl halide, and the like. Some other representative groups may be found in volume 3 of The Peptides, Gross, E. and Meinhofer, J.
  • N-aryl- or -dkylsulfonylation may be carried out in a solvent which does not adversely affect the reaction (e.g., acetone, dichloromethane, tetrahydrofuran, pyridine or NN- dimethylformamide or a mixture thereof).
  • the reaction may be conducted above, at, or below ambient temperature.
  • N-carbamate formations may be ca ⁇ ied out using common protecting groups for amino group such as, but not Umited to methylcarbamates (cyclopropylmethyl, 9- fluorenylmethyl, and the like), substituted ethylcarbamates (2,2,2-trichloroethyl, 2- phosphonoethyl, 2-methylthioethyl, and the like), substituted propyl and isopropylcarbamates (1,1-dimethylpropynyl, 1 -methyl- l-(4-biphenylyl)ethyl, tert-butyl, phenyl, p-nitrobenzyl, 8- quinolyl, N-hydroxypiperidinyl, benzyl, dimethoxybenzyl, 9-anthrylmethyl, 1-adamantyl, cyclohexyl, tert-amyl, cinnamoyl, isobutyl, N'-p-
  • N-carbamates and other groups may be found in volume 3 of The Peptides, Gross, E. and Meinhofer, J. Academic Press, 1981 and Protective Groups in Organic Synthesis, Greene, T. W. John Wiley & Sons, New York, Chapter 7, 1981.
  • the N-carbamate formation may be carried out in a solvent which does not adversely affect the reaction (e.g., acetone, dichloromethane, tetrahydrofuran, pyridine or NN-dimethylformamide or a mixture thereof).
  • the reaction may be conducted above, at, or below ambient temperature.
  • N-guanidium formation may be ca ⁇ ied out using several common reagents such as l-guanyl-3,5-dimethylpyrazole (Salvadori, S.; Sarto, G. P.; Tomatis, R. Eur. J. Med. Chem. Chim. Ther. 1983, 18, 489), O-methylisourea (Van ⁇ ispen, J. W.; Tesser, G. I.; ⁇ ivard, R. J. F. Int. J. Peptide Protein Res. 1977, 9, 193), and thiourea sulf onylate (Maryanoff, C. A.; Stanzione, R. C; Plampin, J.
  • the N-guanidinium formation may be carried out in a solvent which does not adversely affect the reaction (e.g., acetone, dichloromethane, tetrahydrofuran, pyridine or NN-dimethylformamide or a mixture thereof).
  • the reaction may be conducted above, at, or below ambient temperature.
  • N-sulfenamides may be prepared from an amine and a sulfenyl halide (Davis, F. A.; Nadir, U. K. Org. Prep. Proc. Int. 1979, 11, 33; Kobayashi, T.; lino, K.; Hiraoka, T. /. Am. Chem. Soc. 1977, 99, 5505; Zervas, L.; Borovas, D.; Gazis, E. J. Am. Chem. Soc. 1963, 85, 3660).
  • Suitable reagents include, but are not Umited to benzenesulfenyl halide, o-nitrobenzenesulfenyl halide, 2,4-dinitrosulfenyl halide, pentachlorobenzenesulfenyl halide, 2-nitro-4-methoxybenzenesulfenyl halide, triphenylmethylsulfenyl hatide, and the like.
  • Other groups may be found in volume 3 of The Peptides, Gross, E. and Meinhofer, J. Academic Press, 1981 and Protective Groups in Organic Synthesis, Greene, T. W. John Wiley & Sons, New York, Chapter 7, 1981.
  • the N-sulfenylation may be carried out in a solvent which does not adversely affect the reaction (e.g., acetone, dichloromethane, tetrahydrofuran, pyridine or NN-dimethylformamide or a mixture thereof).
  • a solvent which does not adversely affect the reaction
  • the reaction may be conducted above, at, or below ambient temperature.
  • suitable halogenation reagents include, but are not Umited to triphenylphosphine with halogens (Verheyden, J. P. H.; Moffatt, J. G. /. Am. Chem. Soc. 1964, 86, 2093; Bergman, R. G. ibid., 1969, 91, 7405; Hrubiec, R. T.; Smith, M. B. /. Org. Chem., 1983, 48, 3667), triphenylphosphine with cyanogen halides (Homer, L.; Oediger, H.; Hoffmann, H. Annalen Chem.
  • halogenation may also be accompUshed by other reagents such as mono- or tri-alkylsUyl halides with or without sodium halides (Olah, G. A.; Husain, A.; Singh, B. P.; Mehrota, A. K. /. Org. Chem. 1983, 48, 3667; Balme, G.; Fournet, G.; Gore, J. Tetrahedron Lett.
  • the halogenation may be ca ⁇ ied out in a solvent which does not adversely affect the reaction (e.g., acetone, dichloromethane, tetrahydrofuran, pyridine or NN- dimethylformamide or a mixture thereof).
  • a solvent which does not adversely affect the reaction
  • the reaction may be conducted above, at, or below ambient temperature.
  • phosphonic acid ester formation may be ca ⁇ ied out using Michaelis- Arbuzov reactions (Bhattacharya, A. K.; Thyagarajan, G. Chem. Rev. 1981, 81, 415; Bauer, G.; Haegele, G. Angew. Chem. Int. Ed. Engl. 1977, 16, 477).
  • the phosphonic acid ester formation may be carried out in a solvent which does not adversely affect the reaction (e.g., acetone, dichloromethane, tetrahydrofuran, pyridine or NN-dimethylformamide or a mixture thereof).
  • a solvent which does not adversely affect the reaction e.g., acetone, dichloromethane, tetrahydrofuran, pyridine or NN-dimethylformamide or a mixture thereof.
  • the reaction may be conducted above, at, or below ambient temperature.
  • phosphorylation may be carried out using, but is not Umited to the 2- halo-2-oxo- 1, 3, 2-dioxaphospholane-triethylamine reaction (Chandrarakumar, ⁇ . S.; Hajdu, J. J. Org. Chem. 1983, 48, 1197).
  • the phosphorylation may be carried out in a solvent which does not adversely affect the reaction (e.g., benzene, toluene, acetone, dichloromethane, tetrahydrofuran or N,N-dimethylformamide or a mixture thereof).
  • reaction is preferably conducted in the presence of organic or inorganic bases, as described in process (a), preferably in the presence of organic bases such as triethylamine, pyridine etc.
  • organic bases such as triethylamine, pyridine etc.
  • the reaction may be conducted above, at, or below ambient temperature, more preferably from 0 to 50 °C.
  • thioether formation may be ca ⁇ ied out using, but is not limited to aryl- or alkylmercaptan in the presence of suitable tert-amines such as tiialkylamine, pyridine, and the like.
  • the reaction may also be carried out by a metal-catalyzed thioether formation (Guindon, Y; Frenette, R; Fortin, R.; Rokach, J. J. Org. Chem. 1983, 48, 1357), alkali metal salts of aryl- or alkylmercaptans with a compound of formula I which contains CH-OLg group (OLg is the leaving group).
  • the alkali metal may be selected from sodium, potassium, lithium, and cesium.
  • the thioether formation may be ca ⁇ ied out in a solvent which does not adversely affect the reaction (e.g. acetone, dichloromethane, tetrahydrofuran, pyridine, NN- dimethylformamide, etc. or a mixture thereof).
  • a solvent which does not adversely affect the reaction (e.g. acetone, dichloromethane, tetrahydrofuran, pyridine, NN- dimethylformamide, etc. or a mixture thereof).
  • the reaction may be conducted above, at, or below ambient temperature.
  • aryl- or alkyloxythiocarbonylation may be carried out using aryl- or alkyloxythiocarbonylchloride or co ⁇ esponding halides in the presence of suitable tert-amines such as tiialkylamine, pyridine, and the like.
  • suitable tert-amines such as tiialkylamine, pyridine, and the like.
  • the aryl- or alkylthiocarbonylation may be ca ⁇ ied out in a solvent which does not adversely affect the reaction (e.g. acetone, dichloromethane, tetrahydrofuran, pyridine, NN-dimethylformamide etc. or a mixture thereof).
  • the reaction may be conducted above, at, or below ambient temperature.
  • ether formation may be ca ⁇ ied out using, for example, aryl-, arylalkyl- , (heterocyclic)alkyl-, (heterocyclic)alkenyl-, (heterocyclic)alkynyl-, loweralkoxycarbonylalkyl-, arylalkoxycarbonylalkyl-, arylalkylcarbonylalkyl-, trialkylsilylcarbonylalkyl-, trialkyl-stannylcarbonylalkyl-, amidocarbonylalkyl-, alkylamidocarbonylalkyl-, dialkylamido-carbonylalkyl-, arylamidocarbonylalkyl-, alkylamidocarbonylalkyl-, heterocyclicamido-carbonylalkyl-, heterocycUc or alkylhalides in the presence of KY-zeoUte (Onaka, M.; Kawai, M.
  • the ether formation may also be carried out with dialkyl- or diarylphosphoric acid in the presence of p-toluenesulfonic acid (Kashman, Y. J. Org. Chem. 1972, 37, 912), with diazo compounds with tin(E) chloride (Christensen, L. F.; Broom, A. D. J. Org. Chem. 1972, 37, 3398), or with 2,2,2-trichloroalkanols in the presence of base (Corey, E. J.; Link, J. O.
  • ether formation may be accomplished with a suitable trichloroacetimidate in the presence of an acid catalyst (Wessel, H. P.; Iversen, T.; Bundle, D. R. J. Chem. Soc. Perk Trans. 1985, 7, 2247.)
  • the ether formation may be carried out in a solvent which does not adversely affect the reaction (e.g. acetone, dichloromethane, tetrahydrofuran, pyridine, NN-dimethylformamide, ether, cyclohexane, etc. or a mixture thereof).
  • the reaction may be conducted above, at, or below ambient temperature. More specifically, O-alkylation may be carried out using bromoacetic acid derivatives, iodoacetic acid derivatives, trifluoromethanesulfonyloxy acetic acid derivatives, chloro- bromo- or iodomethanesulfonic acid derivatives, chloro- bromo- or iodoacetyltrimethylsUane and the like in the presence of an appropriate base such as triethylamine, potassium fluoride or silver(I) oxide.
  • the reaction is performed in an inert solvent such as N,N-dimethylformamide, acetonitrile or dichloromethane, preferably between -50 °C and 80 °C.
  • alkylation can be carried out using alkyl-, or arylalkyl- diazoacetates in the presence of a metal catalyst, for example Rh(OAc) 2 in an inert solvent such as dichloromethane preferably between -20 °C and 80 °C.
  • a metal catalyst for example Rh(OAc) 2 in an inert solvent such as dichloromethane preferably between -20 °C and 80 °C.
  • N-cyclic imide formations may be carried out using phthalic anhydride (Sasaki, T.; Minamoto, K.; Itoh, H. J. Org. Chem. 1978, 43, 2320), o -methoxycarbonyl- benzoyl chloride with trialkylamine (Hoogwater, D. A.; Reinhoudt, D. ⁇ .; Lie, T. S.; Gunneweg, J. J.; Beyerman, H. C. Reel. Trav. Chim. Pays-Bas. 1973, 92, 819), orN- ethoxycarbonylphthalimide ( ⁇ efkens, G. H. L.; Tesser, G.
  • N- cyclic imide formation may be ca ⁇ ied out in a solvent which does not adversely affect the reaction (e.g. acetone, dichloromethane, tetrahydrofuran, pyridine, NN-dimethylformamide, etc. or a mixture thereof).
  • the reaction may be conducted above, at, or below ambient temperature.
  • deoxygenation may be carried out using, but is not Umited to phenoxythiocarbonyl derivative with tributyltin hydride and 2,2-azobis-2-methylpropionitrile (AIB ⁇ ) (Robins, M. J.; Wilson, J. S.; Hansske, F. J. Am. Chem. Soc. 1983, 705, 4059; Barton, D. H. R.; McCombie, S. W. J. Chem.
  • suitable oxidizing reagents include activated dialkyl sulfoxides (e.g. dimethylsulfoxide, methylethylsulfoxide) (Mancuso, A. J.; Swem, D. Synthesis 1981, 165), organo chromates [e.g. pyridinium chlorochromate (Corey, E. J.; Suggs, J. W. Tetrahedron Lett. 1975, 2647; Corey, E. J.; Boger, D. L. Tetrahedron Lett. 1978, 2461), pyridinium dichromate (Corey, E. J.; Schmidt, G. Tetrahedron Lett. 1979, 5, 399), Collins reagent (Collins, J.
  • activated dialkyl sulfoxides e.g. dimethylsulfoxide, methylethylsulfoxide
  • organo chromates e.g. pyridinium chlorochromate (Corey, E. J.; Suggs,
  • the oxidation may be carried out in a solvent which does not adversely affect the reaction (e.g. acetone, dichloromethane, tetrahydrofuran, pyridine, NN-dimethylformamide, etc. or a mixture thereof).
  • the reaction may be conducted above, at, or below ambient temperature.
  • suitable alkylating reagents include, but are not limited to aldehydes and ketones in the presence of reducing agents (Hrubowchak, D. M.; Smith, F. X. Tetrahedron Lett. 1983, 24, 4951), alkyl-, aryl, or arylalkyl haUdes (Shono, T.; Kashimura, S.; Sawamura, M.; Soejima, T. J. Org. Chem. 1988, 53, 907).
  • an organic or inorganic bases such as an alkaUne earth metal (e.g. calcium, balium, magnesium, thallium etc.), an alkali metal hydride (e.g.
  • an alkali metal hydroxide e.g. sodium hydroxide, potassium hydroxide, etc.
  • an alkali metal carbonate e.g. sodium carbonate, potassium carbonate, etc.
  • an alkali metal hydrogen carbonate e.g. sodium hydrogen carbonate, potassium hydrogen carbonate, etc.
  • an alkali metal alkoxide e.g. sodium methoxide, sodium ethoxide, thalUum ethoxide, potassium tert-butoxide, etc.
  • an alkali metal alkanoic acid e.g. sodium acetate, etc.
  • a trialkylamine e.g.
  • a pyridine compound e.g. pyridine, lutidine, picoUne, 4-N ⁇ V-dimethylaminopyridine, etc.
  • quinoUne and the like.
  • the alkylation may be carried out in a solvent which does not adversely affect the reaction (e.g. acetone, dichloromethane, tetrahydrofuran, pyridine, NN-dimethylformamide, etc. or a mixture thereof).
  • the reaction may be conducted above, at, or below ambient temperature.
  • suitable halogenation reagents include, but are not limited to halogens treated by i ⁇ adiation (sun lamp) for several hours (Heffher, R.; Safaryn, J. E.; Joullie, M. M.; Tetrahedron Lett. 1987, 28, 6539) or oxalyl chloride (Evans, D. A.; Dow, R. L.; Shih, T. L.; Takecs, J. M.; Zahler, R. J. Am. Chem. Soc. 1990, 772, 5290).
  • the halogenation may be ca ⁇ ied out in a solvent which does not adversely affect the reaction (e.g. acetone, dichloromethane, tetrahydrofuran, pyridine, NN-dimethylformamide, etc. or a mixture thereof).
  • the reaction may be conducted above, at, or below ambient temperature.
  • suitable oxidation reagents include, but are not limited to oxodiperoxymolybdenum yridine)- 1 ,3-dimethyl-3,4,5,6-tetrahydro-2( lH)-pyrimidinone (Anderson, J. C; Smith, S. C. S1W E7T 1990, 2, 107) and oxodiperoxymolybdenum(pyridine)-hexamethylphosphoramide (Vedejs, E. J. Am. Chem. Soc. 1974, 96, 5944; Vedejs, E.; Engler, D. A.; Telschow, J. E. J. Org. Chem. 1978, 43, 188).
  • the oxidation may be carried out in a solvent which does not adversely affect the reaction (e.g. acetone, dichloromethane, tetrahydrofuran, pyridine, NN-dimethylformamide, etc., or a mixture thereof).
  • a solvent which does not adversely affect the reaction
  • the reaction may be conducted above, at, or below ambient temperature.
  • suitable olefination reagents include, but are not Umited to Wittig reagents (Maecker, M., Org. React. 1965, 14, 270; Johnson, A. W., " Ylid Chemistry,” Academic Press, New York, 1966) and CH 2 I 2 -Zn-TiCl4 [or Ti(NEt 2 )4] reagent (Hibino, J.; Okazoe, T.; Takai, K.; Nozaki, H. Tetrahedron Lett. 1985, 26, 5579; Okazoe, T.; Hibino, J.; Takai, K.; Nozaki, H. ibid. 1985, 26, 5581).
  • the carbonyl olefination may be carried out in a solvent which . does not adversely affect the reaction (e.g. acetone, dichloromethane, tetrahydrofuran, pyridine, NN-dimethylformamide, etc., or a mixture thereof).
  • the reaction may be conducted at room temperature.
  • suitable O-acylation reagents include, but are not Umited to alkyl, aryl, or arylalkyl acyl halides (Lakhvich, F. A.; Khlebnicova, T. S.; Akhrem, A. A. Synthesis 1985, 8, 784).
  • the O-acylation may be carried out in a solvent which does not adversely affect the reaction (e.g. acetone, dichloromethane, tetrahydrofuran, pyridine, NN- dimethylformamide, etc., or a mixture thereof).
  • the reaction may be conducted above, at, or below ambient temperature.
  • suitable amination reagents include, but are not Umited to amino acid derivatives and lower alkyl, aryl, or arylalkyl amines (Winkler, J. D.; Hershberger, P. M.; Springer, J. P. Tetrahedron Lett. 1986, 27, 5177).
  • the reaction may be carried out in refluxing in benzene, toluene or a solvent which does not adversely affect the reaction (e.g. tetrahydrofuran, pyridine, NN-dimethylformamide, etc., or a mixture thereof).
  • the reaction may be conducted at room temperature.
  • the alkyUdene formation may be ca ⁇ ied out using, but is not Umited to aldehydes and ketones with active methylene compounds. (Schonberg, A.; Singer, E. Chem. Ber. 1970, 103, 3871; Chatterjee, S. . Chem. Soc. B, 1969, 725).
  • the alkyUdene formation may be carried out in a solvent which does not adversely affect the reaction (eg. acetone, dichloromethane, tetrahydrofuran, pyridine, NN-dimethylformamide, etc., or a mixture thereof).
  • the reaction may be conducted under cooling to heating.
  • L may be hydroxy, or a good leaving group (halogen, tosylate, mesylate or ttiflate, for example).
  • the elimination of H 2 O may be carried out in a solvent which is inert under the reaction conditions (e.g. toluene) with a trace of acid (e.g. toluenesulfonic acid), at a temperature selected from 50 to 100 °C.
  • the precursor compound contains a good leaving group
  • the elimination may be carried out in the presence of a base (e.g. triethyl amine or potassium carbonate), at a temperature selected from 0 to 100 °C.
  • suitable diamines include phenylene diamine and substituted 1,2- phenyl diamines, 2,3-diaminopyridine, 3,4-diaminopyridine, 4,5-diaminopyridazine, 4,5- diaminopyrimidine and their acid salts, preferably in the presence of tertiary amines (e.g. N- methylmorpholine).
  • Suitable solvents include methanol, ethanol, propanol, acetonitrile, 2- butanone and NN-dimethylformamide, and a reaction temperature selected from 50 to 100 °C.
  • suitable reagents include sodium borohydride, zinc in acetic acid, sodium triacetoxyborohydride in acetic acid, lithium trialkoxyaluminum hydride in tetrahydrofuran, potassium or lithium tri-_.ec-butylborohydride in tetrahydrofuran, and borane/t-butylamine complex in a solvent such as methanol or ethanol.
  • the reduction may be conducted at -70 °C to room temperature.
  • suitable 2-aminothiophenols include substituted 1,2- aminothiophenols, preferably in the presence of tertiary amine (e.g. N-methylmorpholine).
  • Suitable solvents include methanol, ethanol and n-propanol; and the reaction may be conducted at a temperature selected from 50 to 100 °C.
  • the reagent to be used in this reaction may include di(lower)alkyl sulfoxide (e.g. dimethyl sulfoxide, ethyl methyl sulfoxide, propyl methyl sulfoxide, isobutyl methyl sulfoxide, butyl methyl sulfoxide, isobutyl methyl sulfoxide, hexyl methyl sulfoxide, etc).
  • di(lower)alkyl sulfoxide e.g. dimethyl sulfoxide, ethyl methyl sulfoxide, propyl methyl sulfoxide, isobutyl methyl sulfoxide, butyl methyl sulfoxide, isobutyl methyl sulfoxide, hexyl methyl sulfoxide, etc).
  • This reaction is usually conducted in the presence of oxalyl chloride, acid chlorides, lower alkanoic anhydride such as acetic anhydride in a conventional solvent that does not adversely influence the reaction such as dichloromethane, acetone, ethyl acetate, tetrahydrofuran, pyridine, N ⁇ V-dimethylformamide, etc., followed by the addition of a tertiary amine (e.g. triethyl amine).
  • a tertiary amine e.g. triethyl amine
  • the dithiols are lower alkyl dithiols (e.g. ethanedithiol, propanedithiol or butanedithiol) and 1,2-aryl dithiols (e.g. 1,2-benzenedithiol) in the presence of a Lewis acid (e.g. boron trifluoride etherate or lanthanum trichloride) in a conventional solvent that does not adversely influence the reaction such as dichloromethane, tettahydrofuran or ether.
  • a Lewis acid e.g. boron trifluoride etherate or lanthanum trichloride
  • the reaction may be conducted at -70 °C and room temperature.
  • suitable oxygen-substituted amines include hydroxyl amine, O- alkylhydroxyl amines, and O-arylalkyl hydroxyl amines, for example O-benzyl hydroxyl amine.
  • Suitable solvents include those that do not adversely affect the reaction, for example ethanol or methanol. The reaction is preferably carried out with one equivalent of hydroxyl amine, and at a temperature of 25 to 100 °C, more preferably at the reflux temperature of the solvent.
  • suitable hydrazines include alkylhydrazines (e.g. butylhydrazine), arylhydrazines (e.g. phenylhydrazine), acylhydrazines (e.g. acetylhydrazine), semicarbazides (e.g. t-butyloxycarbonyl hydrazine) and sulfonyl hydrazines (e.g. tosyl hydrazine) in a conventional solvent that does not adversely affect the reaction such as tettahydrofuran, methanol or ethanol.
  • the reaction may be conducted at 20 to 100 °C.
  • 2-substitutions on the pyrimidine may be hydrogen, alkyl, aryl, hydroxyl, alkoxy, thiol, amino, alkylamino, arylamino, acylamino, carbamylamino, and sulphonylamino groups.
  • the appropriate pyrimidine containing compounds may be prepared according to the methods described in " The Chemistry of Heterocyclic Compounds, Vol.16, supplement II, Chapter E, pp 21-60", D. J. Brown, John Wiley & Sons, 1985.
  • the furan containing compounds may be prepared according to the method described by Paulissen, R., et. al. in Tetrahedron Lett. 1974, 607.
  • process (oo) one equivalent of hydroxyl amine hydrochloride and tertiary amine (e.g. N-methylmorphoUne) in a conventional solvent that does not adversely affect the reaction such as tetrahydrofuran, methanol, ethanol or isopropanol is used to prepare the compound.
  • the reaction is conducted at 20 to 100 °C.
  • the pyridine containing compounds may be prepared according to the literature: Osman, A. ⁇ .; Ismail, M. M.; Barakat, M. A. Rev. Roum. Chim. 1986, 31, 615- 624; Ried W.; Meyer, A., Ber. Deutsch. Chem. Ges. 1957, 90, 2841; Troschutz, R.; Troschultz, J.; SoUhuberkretzer, M. Arch Pharm. 1985, 318, 777-781.
  • a substituted 2-aminothiophenol, a 2-aminophenol or an aromatic 1,2- diamine is used in a conventional solvent that does not adversely affect the reaction such as tetrahydrofuran, ethanol, isopropanol, acetonitrile or NN-dimethylformamide.
  • the reaction may be conducted at 20 to 100 °C.
  • the keto-substituted furan containing compound may be prepared according to the literature: WilUams, P. H. et al, /. Am. Chem. Soc. 1960, 82, 4883; E. J. Corey et al., Chem. Lett. 1987, 223.
  • suitable l-halo-2-nitroaromatics may be substituted l-fluoro-2- nitrobenzene, o-fluoro-nitropyridines, or o-bromo-nitto-naphthalene, etc.
  • the arylation may be carried out in a solvent which does not adversely affect the reaction (e.g. tettahydrofuran, NN-dimethylformamide, dimethoxyethane, diglyme, etc.).
  • the base used to generate the anion may be isopropyl magnesium chloride, lithium diisopropyl amine or sodium hydride.
  • the reaction may be conducted at a temperature selected from -70 °C to 100 °C.
  • a nittile oxide may be formed either by oxidation of an aldoxime or dehydration of a nitro compound as described in the following references or literature cited therein: (1) Torssell, K. G. B. " ⁇ ittile Oxides, ⁇ itrones and ⁇ ittonates in Organic Synthesis”; VCH Publishers: New York, 1988, p 64; (2) Kim, J. N.; Ryu, E. K. Synthetic Communications 1990, 20, 1373; (3) Chow, Y. L.; Shy, Y. Y.; Bakker, B. H.; PUlay, K. S. Heterocycles 1989, 29, 2245.
  • the nittile oxide is placed in the presence of an alpha,beta- unsaturated enone in an inert solvent to yield an 2-isoxazoUnes. Any isomers may subsequently be chomatographically separated.
  • an isoxazoUne may be transformed to the co ⁇ esponding beta-hydroxy ketone using but is not limited to molybenum hexacarbonyl in wet acetonitrile according to: Baraldi, P. G.; Barco, A.; Benetti, S.; Manfredini, S.; Simoni, D. Synthesis 1987, 276.
  • Ti 3+ may be employed to attain N-O bond cleavage: Das, N. B.; Torssell, K. B. G. Tetrahedron 1983, 39, 2227.
  • Raney-nickel may also selectively cleave the N-O bond without reducing the imino functionality as described in the following reference and literature cited therein: Torssell, K. G. B. "Nittile Oxides, Nittones and Nittonates in Organic Synthesis"; VCH Publishers: New York, 1988, p 16 and 290. During the course of this transformation, a significant amount of dehydration occurs to produce alpha-beta unsaturated enones which may be separated from the beta-hydroxy ketones.
  • an aryl- or alkylsulfonyl hydrazone may be formed by treatment of a ketone with an aryl- or alkylsulfonyl hydrazide in the presence of an acid catalyst in a solvent suitable for the reaction such as methanol or ethanol at temperatures ranging from ambient to the reflux temperature of the solvent.
  • an allyUc alcohol may be produced by selective reduction of an alpha-beta unsaturated enone. This is accomplished with but not Umited to sodium borohydride in the presence of cerium(IE) chloride heptahydrate in a suitable solvent such as methanol at or near 0 "C.
  • an epoxide may be produced on the central carbonyl of a tricarbonyl moiety by but not Umited to excess diazomethane as described in: Fisher, M. J.; Chow, K.; Villalobos, A.; Danishefsky, S. J. /. Org. Chem. 1991, 56, 2900-2907.
  • Uberation of the ester to the acid may be achieved by the cleavage of a suitably substituted ester function.
  • a suitably substituted ester function may be benzyl, 2,2,2- trichloroethyl, 9-fluorenylmethyl and the like. These are cleaved by methods well known to those skilled in the art.
  • condensation of an amine with the acid may be performed using the mixed or symmetrical anhydride of said acid, or an ester of the acid, preferably activated, such as the ester derived from hydroxybenzotriazole, or the co ⁇ esponding acylcyanide, acylimidazole, or acylazide of the aforementioned acid.
  • selective protection of the 32-hydroxyl moiety may be achieved using one of a variety of trialkylsilyl groups. This then leaves exposed a lone secondary alcohol on C-24 for selective inversion, which may be accomplished by activation of the 24-hydroxy as a mesylate, tosylate, etc., followed by inversion with a suitable nucleophile such as water, benzoic acid, formic acid, etc.
  • inversion of the unactivated 24-hydroxy group may be achieved using well described Mitsunobu conditions.
  • condensation of an alkyloxy or substituted alklyoxy carbonyl hydrazine with ascomycin, FK506, similar compounds, or a suitable derivative thereof wherein the C-22 is available as a reactive center, including but not Umited to a carbonyl is performed in an inert solvent such as methanol, ethanol, 2-propanol, etc., in the presence of a catalyst which may be an acid such as formic acid, p-toluenesulfonic acid, or camphor sulfonic acid.
  • L may be a hydroxyl group, or a good leaving group (halogen, tosylate, nittobenzenesulfonate, mesylate or ttiflate, for example).
  • the condensation may be ca ⁇ ied out in a solvent which does not adversely affect the reaction (e.g. isopropanol, acetonitrile, dioxane, NN-dimethylformamide, tettahydrofuran, etc.).
  • the reaction may be ca ⁇ ied out in the presence of base (e.g. triethylamine, 4- methylmorphoUne or magnesium carbonate, etc.), at a temperature selected from 0 to 100 °C.
  • base e.g. triethylamine, 4- methylmorphoUne or magnesium carbonate, etc.
  • the appropriate thiazole containing compound may be prepared according to Hantzsch's synthesis described by: Katritzky, A.R.; Rees, C.W. "Comprehensive Heterocyclic Chemistry”; Pergamon Press: Oxford, 1984, Vol. 6, Part 4B, p.294-299.
  • L may be a hydroxyl group, or a good leaving group (halogen, tosylate, nittobenzenesulfonate, mesylate or ttiflate, for example).
  • the condensation may be ca ⁇ ied out in a solvent which does not adversely affect the reaction (e.g. isopropanol, t-butanol, acetonitrile, dioxane, NN-dimethylformamide, tettahydrofuran, etc.).
  • the reaction may be ca ⁇ ied out in the presence of base (e.g. triethylamine, 4-methylmorpholine, potassium carbonate or magnesium carbonate, etc.), at a temperature selected from 0 to 100 °C.
  • Suitable amidines include formamidine, alkylamidines, arylamidines and alkylisoureas.
  • Suitable guanidines include N-arylguanidines, N-acylated guanidines and N- sulfonylated guanidines.
  • L may be a hydroxyl group, or a good leaving group (halogen, tosylate, nittobenzenesulfonate, mesylate or ttiflate, for example).
  • the condensation may be carried out in a solvent which does not adversely affect the reaction (e.g. isopropanol, t-butanol, acetonitrile, dioxane, NN-dimethylformamide, tettahydrofuran, etc.).
  • the reaction may be carried out in the presence of a base (e.g., triethylamine, 4-methylmorphotine, potassium carbonate or magnesium carbonate), at a temperature selected from 0 to 100 °C.
  • a base e.g., triethylamine, 4-methylmorphotine, potassium carbonate or magnesium carbonate
  • the amides are primary amides such as formamide, alkylacylamides and arylacylamides.
  • the organometalUc reagent may be a Grignard reagent, an alkyllithium, or an aryllithium reagents.
  • the selective addition may be ca ⁇ ied out in a solvent which does not adversely affect the reaction (e.g., hexanes, ether, tettahydrofuran, dimethoxyethane or 2-methoxyethyl ether).
  • the reaction may be ca ⁇ ied out in the presence of cerium (IE) at a temperature selected from -100 °C to O °C.
  • IE cerium
  • the gamma amino alpha hydroxy carbonyl or a masked gamma amino alpha hydroxy carbonyl of a co ⁇ esponding compound prepared by process (sss) may have substitutions (e.g. alkyl, aryl groups, etc.) at the alpha and/or beta positions. Furthermore, the amino group may have N-alkyl or aryl substitutions.
  • the condensation may be carried out in a solvent which does not adversely affect the reaction (e.g. isopropanol, t-butanol, acetonitrile, dioxane, N,N-dimethylformamide, tetrahydrofuran, etc.).
  • the reaction may be ca ⁇ ied out in the presence of a base (e.g. triethylamine, 4-methylmorpholine, potassium carbonate or magnesium carbonate, etc.), at a temperature selected from 0 to 100 °C.
  • a base e.g. triethylamine, 4-methylmorph
  • the reaction is generally carried out in two steps: first the condensation of an alpha diketone or a masked alpha diketone with an l,2-diaminoalk__ne gives a dihydropyrazine. Once the dihydropyrazine has been prepared, it may be oxidized by air in the presence of Pd/C, PtO 2 or other catalysts. Metal oxides (e.g. Mn ⁇ 2 or CuO) may also be used for the aromatization.
  • the condensation and oxidation may be carried out in a solvent which does not adversely affect the reactions (e.g. isopropanol, acetonitrile, dioxane, benzene, toluene, etc.).
  • the reaction may be carried out in the presence of drying agent such as magnesium sulfate or molecular sieves at a temperature selected from 0 °C to 100 °C.
  • a 1,5-dicarbonyl group or a masked 1,5-dicarbonyl group prepared by process (sss) may have substitutions (e.g. alkyl, aryl groups etc.) at the alpha and/or beta positions.
  • the condensation may be carried out with anhydrous ammonia in a solvent which does not adversely affect the reactions (e.g. Uquid ammonia, isopropanol, acetonitrile, dioxane, benzene, toluene, etc.).
  • the reaction may be carried out at a temperature selected from -40 °C to 100 °C.
  • a 1,4-dicarbonyl group or a masked 1,4-dicarbonyl group prepared by process (sss) may have substitutions (e.g. alkyl, aryl groups, etc.) at the alpha position.
  • the condensation and oxidation may be ca ⁇ ied out with anhydrous hydrazine in a solvent which does not adversely affect the reactions (e.g. isopropanol, acetonitrile, dioxane, benzene, toluene, etc.).
  • a drying agent such as magnesium sulfate or molecular sieves at a temperature selected from 0 °C to 100 °C.
  • the thiocarbonate formation may be carried out in a solvent which does not adversely affect the reactions (e.g. toluene, acetone, methylene chloride, tetrahydrofuran or pyridine, etc.).
  • the reaction may be carried out in the presence of a base such as triethylamine, pyridine, dimethylaminopyridine and sodium carbonate at a temperature selected from 0 °C to 100 °C.
  • the thiocarbonylating reagent may be N,N'-thiocarbonyl-diimidazole, N,N-thiocarbonylbis(2-pyridone), thiophosgene, or O-phenylthiochloroformate.
  • the carbonate formation may be carried out in a solvent which does not adversely affect the reactions (e.g. toluene, acetone, butanone, methylene chloride, tettahydrofuran or pyridine etc.).
  • the reaction may be carried out in the presence of a base such as triethylamine, pyridine, dimethylaminopyridine and sodium carbonate at a temperature selected from 0 °C to 100 °C.
  • the carbonylating reagent may be N,N'-carbonyldiimidazole, N,N'-carbonyl-b I y- (2-pyridone), phosgene, triphosgene, ethyl chloroformate, ethyl trichloroacetate, or o- phenylchloroformate.
  • the cyclic phosphonate formation may be ca ⁇ ied out by first reacting a diol from a selected compound with phosphorous trichloride followed by the addition of an appropriate alcohol and amine.
  • the alcohol used may be an alkyl alcohol, or an aryl alcohol.
  • the amine used may be primary or secondary.
  • the cyclic phosphonate formation may be ca ⁇ ied out by directly reacting the diol from a co ⁇ esponding compound with an appropriate alkoxyphophoryl dichloride.
  • the phosphonate formation may be carried out in a solvent which does not adversely affect the reactions (e.g. carbon tettachloride, chloroform, methylene chloride, toluene, tetrahydrofuran, etc.).
  • the reaction may be carried out in the presence of a base such as triethylamine, pyridine, dimethylaminopyridine, and sodium carbonate at a temperature selected from 0 °C to 100 °C.
  • the reduction of thiocarbonate may be carried out in a solvent which does not adversely affect the reactions (e.g., toluene or tettahydrofuran) at a temperature selected from 0 °C to 100 °C.
  • a solvent which does not adversely affect the reactions (e.g., toluene or tettahydrofuran) at a temperature selected from 0 °C to 100 °C.
  • the reducing agent used may be trimethylphosphite, triethylphosphite, trialkylphosphite or tti-n-butyltin hydride.
  • the reduction of a 1,2-dicarbonyl group of a co ⁇ esponding compound may be ca ⁇ ied out in a solvent which does not adversely affect the reactions (e.g., methanol, ethanol, ethanol, pyridine or N,N-dimethylformamide).
  • a solvent which does not adversely affect the reactions (e.g., methanol, ethanol, ethanol, pyridine or N,N-dimethylformamide).
  • the reducing agents used may be tin amalgam, aluminum amalgam with hydrogen chloride in ethanol, or may be hydrogen sulfide in pyridine or N,N-dimethylformamide.
  • the reducing agents used may be hydrogen gas over Pd/C, or Pt/C, zinc dust with ammonium chloride, zinc dust with hydrochloric acid at a temperature selected from 0 °C to 100 °C.
  • triazole formation may be ca ⁇ ied out using, but is not Umited to an azide derivative with suitable acetylene analogues include diethylacetylene dicarboxylate, dimethylacetylene dicarboxylate, methyl cyanoacetylenecarboxylate, and the likes.
  • the reaction may be conducted above, or below ambient temperature, more preferably from 0 to 50 °C.
  • py ⁇ ole formation may be carried out using, but is not limited to amine compounds with 1,4-dicarbonyl analogues, such as acetonylacetone, and the likes.
  • Suitable solvents include methanol, ethanol, n-propanol, isopropanol, acetonitrile and N,N-dimethylformamide.
  • the reaction may be conducted above, or below ambient temperature, more preferably from 50 to 100 °C.
  • suitable reagents for vicinal hydroxylation include osmium tettaoxide, potassium permanganate, and iodine in conjunction with silver acetate.
  • Osmium tettoxide is preferably used with a regenerating agent such as hydrogen peroxide, alkaline t- butyl hydroperoxide or N-methylmorphoUne-N-oxide, and a solvent that does not adversely affect the reaction, for example diethyl ether or tettahydrofuran.
  • Potassium permanganate is preferably used in mild conditions, for example alkaUne aqueous solution or suspensions. Co-solvents such as t-butanol or acetic acid may also be used.
  • Iodine-silver acetate under 'wet' conditions yields ci-diols.
  • iodine is used in aqueous acetic acid in the presence of silver acetate.
  • Iodine-silver acetate under 'dry' conditions yields trans-diols.
  • the initial reaction is carried out in the absence of water, and final hydrolysis yields the diol.
  • the oxidation is preferably ca ⁇ ied out at a temperature of 0 to 100 °C.
  • Suitable reagents for the oxidative cleavage of the vicinal diol include lead tetraacetate, phenyliodoso acetate, periodic acid or sodium metaperiodate.
  • Suitable solvents for the first two reagents include benzene and glacial acetic acid.
  • the second two reagents are preferably used in aqueous solution. The reaction is preferably carried out at a temperature of 0 to 100 °C.
  • suitable reagents for the oxidation of an aldehyde of the co ⁇ esponding compound may include silver oxide, chromic acid and potassium permanganate.
  • oxygen may also be used in converting an aldehyde to a carboxylic acid of a co ⁇ esponding compound.
  • the catalysts may be palladium or platinum oxide.
  • the air oxidation may be ca ⁇ ied out in a solvent which does not adversely affect the reaction (e.g., ethanol, water, acetonitrile, aqueous acetone or pyridine) at a temperature of 0 to 100 °C.
  • esters of a co ⁇ esponding carboxylic acid may be prepared under neuttal conditions at room temperature by the reaction of the carboxyUc acid with alcohols in the presence of molar amounts of activating reagents such as triphenyl phosphine and diethyl azodicarboxylate, carbodnmides, N,N'-carbonyldiimidazole and l-methyl-2-halopyridinium iodide.
  • activating reagents such as triphenyl phosphine and diethyl azodicarboxylate, carbodnmides, N,N'-carbonyldiimidazole and l-methyl-2-halopyridinium iodide.
  • Esters may also be formed by reacting the co ⁇ esponding carboxylic acid with diazoalkanes in a solvent which does not adversely affect the reaciton (e.g., ether, tetrahydrofuran or methylene chloride) at a temperature of from 0 to 100 °C.
  • a solvent which does not adversely affect the reaciton (e.g., ether, tetrahydrofuran or methylene chloride) at a temperature of from 0 to 100 °C.
  • the cyclopropanation of the allyl group of a co ⁇ esponding compound may be ca ⁇ ied out with diazoalkanes in a solvent which does not adversely affect the reaction (e.g., ether, methylene chloride or tettahydrofuran) in the presence of a catalyst such as palladium (II) acetate.
  • a solvent which does not adversely affect the reaction (e.g., ether, methylene chloride or tettahydrofuran) in the presence of a catalyst such as palladium (II) acetate.
  • the temperature of the reaction is of -15 to 5 °C.
  • a py ⁇ le ring may be produced by reacting a 1,4-dicarbonyl group of a co ⁇ esponding compound with ammonia, or a substituted amine such as benzylamine or 2- aminoethanol.
  • Suitable solvents include those which do not adversely affect the reaction (e.g., methylene chloride, tetrahydrofuran or dioxane). The reaction is preferably ca ⁇ ied out at a temperature of 0 to 100 °C.
  • the cyclization of a 1,4-dicarbonyl group of a co ⁇ esponding compound may be carried out in the presence of a catalytic amount of acid (e.g., acetic acid or arylsulfonic acid).
  • the reaction may be ca ⁇ ied out in a solvent which does not adversely affect the reaction (e.g., methylene chloride, ether, benzene or toluene).
  • the reaction is preferably carried out at a temperature of 0 to 60 °C.
  • suitable reagents include air, a palladium (E) haUde (e.g. palladium (E) chloride), in conjunction with a cuprous halide (e.g. cupper (I) chloride).
  • Suitable solvents include those that do not adversely affect the reaction (e.g. DMF and water). The reaction is preferably ca ⁇ ied out at a temperature of 0 to 100 °C.
  • suitable reducing agents include but are not limited to sodium cyanoborohydride, lithium aluminum hydride, borane-pyridine, or hydrogen in the presence of such catalysts as Raney nickel, platinum, platinum oxide, or palladium.
  • An acidic environment may promote the reduction in some cases, and acids such as hydrochloric acid or p-toluenesulfonic acid may be added for this purpose.
  • the reduction may be ca ⁇ ied out in a solvent which does not adversely affect the reaction (e.g. ethanol, ethyl acetate).
  • reduction of an oxime to the co ⁇ esponding amine may be accomplished with but not Umited to hydrogenation with a suitable catalyst such as palladium on carbon in a solvent inert to the reaction conditions (e.g. ethanol) at temperatures ranging from 0 to 100 °C.
  • a suitable catalyst such as palladium on carbon in a solvent inert to the reaction conditions (e.g. ethanol) at temperatures ranging from 0 to 100 °C.
  • reduction of an enone to the co ⁇ esponding saturated ketone may be accomplished with but not limited to hydrogenation with a suitable catalyst such as either palladium on carbon or rhodium on alumina in a solvent inert to the reaction conditions (e.g. methanol, ethanol, isopropanol, ethyl acetate) in a temperature range from -78 to 100 °C.
  • a suitable catalyst such as either palladium on carbon or rhodium on alumina in a solvent inert to the reaction conditions (e.g. methanol, ethanol, isopropanol, ethyl acetate) in a temperature range from -78 to 100 °C.
  • isoxazoline formation may be accompUshed by, but not Umited to the following sets of reaction conditions involving a beta-hydroxy oxime.
  • One possible method is to treat the beta-hydroxy oxime with Martin's sulfurane dehydrating reagent at or near room temperature in a solvent inert to the reaction conditions such as methylene chloride.
  • the beta-hydroxy oxime may be tteated with p-toluenesulfonyl chloride in a solvent such as pyridine at temperatures ranging from 0 to 100 °C.
  • an intramolecular aldol reaction may be accomplished by, but is not limited to treatment of a carbonyl with a base such as potassium or sodium hydride in a solvent which is inert to the reaction conditions (e.g. tettahydrofuran or N,N- dimethylformamide) at a temperature range from -78 to 150 °C.
  • a base such as potassium or sodium hydride
  • a solvent which is inert to the reaction conditions (e.g. tettahydrofuran or N,N- dimethylformamide) at a temperature range from -78 to 150 °C.
  • a cyclic imine may be formed by, but is not Umited to treatment of an alpha,beta-unsaturated enone with the sodium enolate of a glycine ester imine in an inert solvent such as tetrahydrofuran in a temperature range from -78 to 100 "C.
  • an inert solvent such as tetrahydrofuran in a temperature range from -78 to 100 "C.
  • a substituted py ⁇ ole may be formed by but is not Umited to a 1,3-dipolar cycloaddition between an alpha,beta-unsaturated enone with a glycine ester imine in the presence of a suitable catalyst such as lithium bromide and triethylamine in a solvent inert to the reaction conditions (e.g. tettahydrofuran) at or near room temperature.
  • a suitable catalyst such as lithium bromide and triethylamine in a solvent inert
  • alpha diazoketones can be decomposed by exposure to UV light or by heating.
  • Wolff rea ⁇ angements often ensue yielding beta-keto carboxylic acids when run in a solvent mixture containing water, beta-keto esters when run in a solvent containing an alcohol, or beta-keto amides when run in a solvent containing ammonia, a primary or a secondary amine.
  • aryl-, heterocyclic-, or alkyloxycarbonylation may be ca ⁇ ied out using aryl-, heterocycUc-, or alkyl- chloroformate in the presence of amines like triethylamine, dUsopropylethylamine, pyridine and the like.
  • the reaction may be carried out by reacting the co ⁇ esponding aryl-OH, heterocycUc-OH or alkyl-OH with -CHOC(O)Cl or -CHOC(O)-(p-nittophenyl) in a co ⁇ esponding compound in the presence of amine base.
  • the reaction may be carried out in a solvent which does not adversely affect the reaction (e.g. acetone, dichloromethane, tetrahydrofuran, pyridine and N,N- dimethylformamide, or a mixture thereof).
  • a solvent which does not adversely affect the reaction (e.g. acetone, dichloromethane, tetrahydrofuran, pyridine and N,N- dimethylformamide, or a mixture thereof).
  • the reaction may be conducted above, at or below ambient temperature.
  • In process (zzzz) allylic oxidations may be ca ⁇ ied out using selenium dioxide with or without a co-oxidant, such as tert-butyl hydroperoxide, in an inert solvent such as tettahydrofuran, ether, ethylacetate, water, or a combination thereof.
  • a co-oxidant such as tert-butyl hydroperoxide
  • an inert solvent such as tettahydrofuran, ether, ethylacetate, water, or a combination thereof.
  • the reaction may be conducted at room temperature to 100 °C.
  • the compounds of the present invention are formed by modification of FR-900520 (ascomycin) or one of its congeners (such as FK-506, etc.) by alkylation of the C-32- hydroxyl group with optional modifications exercised at C-18 and/or C-21 and/or C-23 and/or C-24.
  • FR-900520 ascomycin
  • FK-506, etc. congeners
  • alkylation of the C-32- hydroxyl group with optional modifications exercised at C-18 and/or C-21 and/or C-23 and/or C-24.
  • Example 3 The product of Example 3 (0.50 g, 0.59 mmol) was dissolved in dichloromethane (5 mL) and the solution cooled to 0°C. 4-Dimethylaminopyridine (DMAP) (14.4 mg, .0.118 mmol) was added foUowed by l-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (ED AC) (206 mg, 1.07 mmol) then benzylamine (128.3 uL, 1.18 mmol). The reaction was warmed to room temperature and sti ⁇ ed overnight.
  • DMAP 4-Dimethylaminopyridine
  • ED AC l-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride
  • the resultant product of Example 3 (0.8 g, 0.94 mmol) was dissolved in THF (3 mL) and the solution cooled to 0°C before adding N-methylmorpholine (103.4 uL, 0.94 mmol) followed by isobutyl chloroformate (122.2 uL, 0.94 mmol). The resulting suspension was sti ⁇ ed for 20 minutes at 0 °C after which N-methylbenzylamine (243 uL, 1.88 mmol) was added. Sti ⁇ ing was continued overnight as the ice melted.
  • Example 81 The crude isolate from Example 81 (1.5 g, ⁇ 1.2 mmol ) was dissolved in THF (4 mL) and the solution cooled to 0°C before adding N-methylmorpholine (129.4 uL, 1.2 mmol) followed by isobutyl chloroformate (152.8 uL, 0.59 mmol). The resulting suspension was sti ⁇ ed for 20 minutes at 0°C after which ammonium hydroxide (14.8M, 159.2 uL, 2.4 mmol) was added. Sti ⁇ ing was continued overnight as the ice melted.
  • N-methylmorpholine 129.4 uL, 1.2 mmol
  • isobutyl chloroformate 152.8 uL, 0.59 mmol
  • reaction mixture was loaded onto silica (80 mL) in a fritted funnel then eluted with dichloromethane (200 mL), 2:1 hexane/acetone (400 mL), 1:1 hexane/acetone (400 mL), and acetone (200 mL).
  • Fractions containing product were combined and solvent removed in vacuo to give 358 mg yellow foam.
  • the crude product was further purified by RP-HPLC (Rainin Dynamax 41.4 mm phenyl column) eluting with a gradient of 20% methanol/water and acetonitrile to provide the title compound (188.7 mg, 19% yield) as a white foam.
  • MS (FAB)w/z: (M+K) 887.
  • Example 3 The product of Example 3 is activated as in Example 5 and then tteated with methylamine instead of N-methylbenzylamine to provide the title compound.
  • Example 3 The product of Example 3 is activated as in Example 5 and then tteated with dimethylamine instead of N-methylbenzylamine to provide the title compound.
  • the product of Example 3 is activated as in Example 5 and then tteated with ethylamine instead of N-methylbenzylamine to provide the title compound.
  • Example 3 The product of Example 3 is activated as in Example 5 and then treated with N,N- methyl,ethylamine instead of N-methylbenzylamine to provide the title compound.
  • Example 3 The product of Example 3 is activated as in Example 5 and then tteated with propylamine instead of N-methylbenzylamine to provide the title compound.
  • Example 3 The product of Example 3 is activated as in Example 5 and then tteated with N,N-methyl,propylamine instead of N-methylbenzylamine to provide the title compound.
  • the product of Example 3 is activated as in Example 5 and then treated with 2-aminopropane instead of N-methylbenzylamine to provide the title compound.
  • Example 3 The product of Example 3 is activated as in Example 5 and then tteated with N,N-methyl, 2- propylamine instead of N-methylbenzylamine to provide the title compound.
  • Example 3 The product of Example 3 is activated as in Example 5 and then tteated with cyclopropylamine instead of N-methylbenzylamine to provide the title compound.
  • Example 3 The product of Example 3 is activated as in Example 5 and then treated with n-butylamine instead of N-methylbenzylamine to provide the title compound.
  • Example 3 The product of Example 3 is activated as in Example 5 and then tteated with N,N-methylbutylamine instead of N-methylbenzylamine to provide the title compound.
  • the product of Example 3 is activated as in Example 5 and then tteated with isobutylamine instead of N-methylbenzylamine to provide the title compound.
  • the product of Example 3 is activated as in Example 5 and then tteated with N,N-methyl,isobutylamine instead of N-methylbenzylamine to provide the title compound.
  • the product of Example 3 is activated as in Example 5 and then tteated with cyclobutylamine instead of N-methylbenzylamine to provide the title compound.
  • Example 3 The product of Example 3 is activated as in Example 5 and then treated with pentylamine instead of N-methylbenzylamine to provide the title compound.
  • Example 3 The product of Example 3 is activated as in Example 5 and then treated with
  • Example 3 The product of Example 3 is activated as in Example 5 and then tteated with 3-methylbutylamine instead of N-methylbenzylamine to provide the title compound.
  • Example 3 The product of Example 3 is activated as in Example 5 and then treated with N,N-methyl,3- methylbutylamine instead of N-methylbenzylamine to provide the title compound.
  • Example 3 The product of Example 3 is activated as in Example 5 and then treated with cyclopentylamine instead of N-methylbenzylamine to provide the title compound.
  • Example 3 The product of Example 3 is activated as in Example 5 and then tteated with
  • Example 3 The product of Example 3 was activated as in Example 5 and then tteated with
  • Example 3 The product of Example 3 is activated as in Example 5 and then treated with
  • Example 3 The product of Example 3 is activated as in Example 5, and then tteated with 1,2-diaminoethane instead of N-methylbenzylamine to provide the title compound.
  • the product of Example 3 is activated as in Example 5, and then tteated with 1,3-diaminopropane instead of N-methylbenzylamine to provide the title compound.
  • Example 3 The product of Example 3 is activated as in Example 5, and then tteated with
  • Example 3 The product of Example 3 is activated as in Example 5, and then tteated with
  • Example 3 The product of Example 3 is activated as in Example 5, and then tteated with
  • Example 3 The product of Example 3 is activated as in Example 5, and then tteated with
  • the product of Example 3 is activated as in Example 5 and then tteated with 3-biphenylamine instead of N-methylbenzylamine to give the title compound.
  • Example 3 The product of Example 3 is activated as in Example 5 and then treated with N,N-(ethanol-2- yl)-(3-biphenyl)-amine instead of N-methylbenzylamine to give the title compound.
  • Example 3 The product of Example 3 is activated as in Example 5 and then treated with N-phenyl-N-phenyl-N-phenyl-N-phenyl-N-phenyl-N-phenyl-N-phenyl-N-phenyl-N-phenyl-N-phenyl-N-phenyl-N-phenyl-N-phenyl-N-phenyl-N-phenyl-N-phenyl-N-phenyl-N-phenyl-N-phenyl-N-phenyl-N-phenyl-N-phenyl-N-phenyl-N-phenyl-N-phenyl-N-phenyl-N-phenyl-N-phenyl-N-phenyl-N-phenyl-N-phenyl-N-phenyl-N-phenyl-N-phenyl-N-phenyl-N-phenyl-N-phenyl-N-phenyl-N-phenyl-N-
  • Example 3 The product of Example 3 is activated as in Example 5 and then treated with N-phenyl-N',N'- dimethyl-ethyldiamine instead of N-methylbenzylamine to give the title compound.
  • Example 3 The product of Example 3 was activated as in Example 5 and then tteated with
  • the product of Example 3 is activated as in Example 5 and then treated with dicyclohexylamine instead of N-methylbenzylamine to give the title compound.
  • the product of Example 3 was activated as in Example 5 and then treated with 1 equivalent of 4-aminomorpholine and 0.1 equivalents of 4-dimethylaminopyridine instead of N- methylbenzylamine to give the title compound.
  • MS (FAB) m/z: M+K 972.
  • Example 3 The product of Example 3 was activated as in Example 5 and then tteated with thiomorpholine instead of N-methylbenzylamine to give the title compound.
  • MS (FAB) m/z: M+K 973.
  • Example 3 The product of Example 3 was activated as in Example 4 and then tteated with
  • Example 3 The product of Example 3 is activated as in Example 5 and then tteated with methylcarbazate instead of N-methylbenzylamine to give the title compound.
  • the product of Example 3 is activated as in Example 5 and then tteated with L-prolinecarboxamide instead of N-methylbenzylamine to give the title compound.
  • Example 3 The product of Example 3 is activated as in Example 5 and then tteated with L-prolinol instead of N-methylbenzylamine to give the title compound.
  • Example 3 The product of Example 3 is activated as in Example 5 and then treated with D-prolinol instead of N-methylbenzylamine to give the title compound.
  • Example 3 The product of Example 3 is activated as in Example 5 and then tteated with N-(ethanol-)
  • Example 3 The product of Example 3 is activated as in Example 5 and then tteated with
  • Example 3 The product of Example 3 is activated as in Example 5 and then treated with 3-(4- fluoroanilino)-l-propanol instead of N-methylbenzylamine to give the title compound.
  • Example 68 The product of Example 68 is tteated with succinic anhydride, as published in Tetrahedron Letts. 1989, 30, 5045-48, to give the title compound.
  • Example 3 The product of Example 3 was activated as in Example 5 and then tteated with isonicotinic acid hydrazide instead of N-methylbenzylamine to give the tide compound.
  • the product of Example 3 was activated as in Example 5 and then treated with m-fluoroamline instead of N-methylbenzylamine to give the title compound.
  • MS (FAB) m/z: M+2K-H 1045.
  • Example 3 The product of Example 3 is activated as in Example 5 and then tteated with
  • Example 3 The product of Example 3 is activated as in Example 5 and then tteated with 1-naphthylamine instead of N-methylbenzylamine to give the title compound.
  • Example 3 The product of Example 3 is activated as in Example 5 and then tteated with py ⁇ olidine instead of N-methylbenzylamine to provide the title compound.
  • Ascomycin (10 g, .012 mol) was dissolved in distiUed CH2CI2 (50 ml).
  • Rhodium (E) acetate dimer 100 mg was added and the mixture cooled to 0 °C.
  • 9-Fluorenylmethyl diazoacetate (3.35 g, .012 mol) was dissolved in CH2CI2 (10 mL) and the solution added to the reaction via syringe pump at a rate of approximately 0.5 mL/hour. Addition was complete in approximately 24 hours.
  • the reaction was sti ⁇ ed at 0 °C for an additional 24 hours then loaded onto siUca (230-400 mesh, 400 g) and the solvent evaporated by airflow in the hood.
  • the adsorbed siUca was layered over fresh silica (800 g) in a 1 L fritted glass funnel.
  • the silica plug was eluted with the following solvents: CH2CI2 (2 L), 3:1 CH2CI2/CH3CN (4 L), 2:1 CH2CI2/CH3CN (3 L), and 1:1 CH2CI2/CH3CN (3 L).
  • Example 80 The resultant product of Example 80 (5.10 g, 5 mmol) was dissolved in CH2CI2 ( 4 5 mL), whereupon piperidine (5 ml) was added. The solution was sti ⁇ ed at room temperature for 2 hours then transfe ⁇ ed to a separatory funnel, diluted with additional CH2CI2 (100 mL), then washed with IN HC1 (2 x 100 mL) and brine (2 x 100 mL). The organic layer was dried (Na2SO4), filtered, and the solvent removed in vacuo to give 5.08 g of a mixture of the title compound and N-(9-fluorenylmethyl)piperidine. MS (FAB) m/z 888 (M+K), 926 (M+2K- H).
  • Example 81 The product of Example 81 (100 mg, .118 mmol) was dissolved in dichloromethane (1 mL) and the solution cooled to 0 °C. HOBT ⁇ 2O (21.6 mg, .142 mmol) was added followed by ED AC (27.1 mg, .142 mmol) then phenethylamine (26.7 ⁇ L, .212 mmol). The reaction was warmed to room temperature and sti ⁇ ed overnight. Dichloromethane (10 mL) was added and the organic phase washed with IN HC1 (2 x 20 mL), saturated bicarbonate solution (2 x 20 mL), and then brine (2 x 20 mL).

Abstract

Immunomodulatory macrocyclic compounds having formula (I) and pharmaceutically acceptable salts, esters, amides and prodrugs thereof, as well as pharmaceutical compositions containing the same, which possess immunosuppressive, antimicrobial, antifungal, antiviral, antiinflammatory and antiproliferative activity, as well as the ability to reverse chemotherapeutic drug resistance.

Description

MACROCYCLIC AMIDE AND UREA TMMUNOMODULATORS
This application is a continuation-in-part of copending United States Patent Application Serial No. 08/149,419, filed November 9, 1993, which is a continuation-in-part of co-pending United States Patent Application Serial No. 08/032,958, filed March 17, 1993, which is a continuation-in-part of co-pending International Patent Application No. PCT/US92/07600, filed September 8, 1992, which is a continuation-in-part of United States Patent Application Serial No. 07/755,208, filed September 5, 1991 and now abandoned.
Field of the Invention
The present invention relates to novel chemical compounds having immunomodulatory activity, and in particular to macrolide immunosuppressants. More particularly, the invention relates to semisynthetic analogs of ascomycin and FK-506, to means for their preparation, to pharmaceutical compositions containing such compounds and to methods of treatment employing the same.
Background of the Invention
The compound cyclosporine (cyclosporin A) has found wide use since its introduction in the fields of organ transplantation and immunomodulation, and has brought about a significant increase in the success rate for transplantation procedures. Undesired side-effects associated with cyclosporine, however, such as nephrotoxicity, have led to a continued search for immunosuppressant compounds having improved efficacy and safety.
Recently, several classes of macrocyclic compounds having potent immunomodulatory activity have been discovered. Okuhara et al., in European Patent Application No. 184162, published June 11, 1986, disclose a number of macrocyclic compounds isolated from the genus Streptomyces. Immunosuppressant FK-506, isolated from a strain of S. tsukubaensis , is a 23-membered macrocyclic lactone represented by formula la, below. Other related natural products, such as FR-900520 (lb) and FR-900523 (lc), which differ from FK-506 in their alkyl substituent at C-21, have been isolated from S. hygroscopicus yakushimnaensi . Yet another analog, FR-900525, produced by S. tsukubaensis, differs from FK-506 in the replacement of a pipecolic acid moiety with a proline group.
FR-900520, also known as ascomycin, has been previously disclosed by Arai et al. in U.S. Patent No. 3,244,592, issued April 5, 1966, where the compound is described as an antifungal agent. Monaghan, R.L., et al ., on the other hand, describe the use of ascomycin as an immunosuppressant in European Patent Application No. 323865, published July 12, 1989. Although the immunosuppressive activity of FK-506 has been clinically confirmed, its toxicity in mammals has limited its utility. The activity of FK-506 has, however, prompted efforts to discover novel analogs of FK-type compounds which possess superior properties. These efforts include the isolation of new fermentation products, the microbial transformation of existing chemical entities, the chemical modification of these macrocyples, and the synthesis of hybrid species derived from smaller synthetic fragments.
1(a): FK-506 R = CH2CH=CH2; n=l
1(b): FR-900520 R = CH2CH ; n=l
1(c): FR-900523 R = CH3; n=l
1(d): FR-900525 R = CH2CH=CH2; n=0
Fermentation products of FK-type compounds include C-21-epi derivatives of FK- 506; a 31-demethylated derivative of FK-506; 31-oxo-FK-506; and compounds derived from FK-506, FR-900523 and FR-900525 which are characterized by the introduction of hydroxy- protecting groups, formation of a double bond by elimination of water between carbons 23 and 24, oxidation of the hydroxy group at carbon 24 to the ketone, and reduction of the allyl side-chain at carbon 21 via hydrogenation. Other published derivatives include those derived from FK-506 and FR-900520 where the lactone ring is contracted to give a macrocyclic ring containing two fewer carbons.
Several microbial transformations of FK-type compounds at carbon 13 have been published, such as the microbial demethylation of FR-900520 to form the to-demethylated 13,31-dihydroxy ring-rearranged derivative of FR-900520; the microbial monodemethylation of FK-506 and FR-900520, respectively; and the microbial demethylation of FR-900520 at C-31, as well as a number of other macrocyclic microbial transformation products.
Numerous chemical modifications of the FK-type compounds have been attempted. These include the preparation of small synthetic fragments of FK-type derivatives; a thermal rearrangement of a variety of derivatives of FK-506 which expands the macrocyclic ring by two carbons; and modifications which include methyl ether and aryl ether formation at C-32 and/or C-24, oxidation of C-32 alcohol to the ketone, and epoxide formation at C-9.
Although some of these modified compounds exhibit immunosuppressive activity, the need remains for macrocyclic immunosuppressants which do not have the serious side effects frequently associated with immunosuppressant therapy. Accordingly, one object of the invention is to provide novel semisynthetic macrolides which possess the desired immunomodulatory activity but which minimize undesired side effects.
Another object of the present invention is to provide synthetic processes for the preparation of such compounds from starting materials obtained by fermentation, as well as chemical intermediates useful in such synthetic processes.
A further object of the invention is to provide pharmaceutical compositions containing, as an active ingredient, one of the above compounds. Yet another object of the invention is to provide a method of treating a variety of disease states, including post- transplant tissue rejection and autoimmune disfunction.
Summary of the Invention
The present invention is directed to compounds having the formula:
and pharmaceutically-acceptable salts, esters, amides and prodrugs thereof, wherein n, R, R1, Rla> R2, R2a, R3, R4 and R5 are specifically defined, which possess immunosuppressive, antimicrobial, antifungal, antiviral, antunflammatory and antiproliferative activity, as well as the ability to reverse chemotherapeutic drug resistance; to pharmaceutical compositions comprising a compound of the invention in combination with a pharmaceutically-acceptable carrier; to processes for the preparation of these compounds; to synthetic intermediates useful in the preparations of these and other immunomodulator derivatives of ascomycin; to methods of formulating pharmaceutical compositions comprising these compounds; and to a method of immunomodulatory treatment of a human or veterinary subject in need of such treatment by the administration of a therapeutically-effective amount of a novel compound according to the present invention.
Detailed Description of the Invention
The instant invention is directed to novel compounds described by the general formula (I):
and pharmaceutically-acceptable salts, esters, amides and prodrugs thereof, wherein:
n is zero or one;
R is hydrogen, methyl, ethyl, allyl, propyl, 2-hydroxyethyl, cyclopropylmethyl, 2-oxopropyl or 2-ethanal;
R1 and Rla are selected such that one of R1 and Rla is hydrogen, -(C1-C6- alkyl)oxy or hydroxy, and the other is chosen from the group consisting of: (I) -O(CH )jC(O)R12, where j is one-to-five, and Rl2 is:
(A) hydroxy;
(B) -OR13, wherein R13 is:
(i) -(Cι-Cιo-alkyl);
(ii) -(cyclo-C3-C8-alkyl);
(iii) -(cyclo-C3-C8-alkyl-Cι-C3-alkyl);
(iv) aryl-(Cι-C6-alkyl)-, where aryl is as defined below, wherein the zero, one, two or three substituents on the aryl group, each designated R301, are independently selected from the group consisting of:
(a) -(Cι-to-C-7-alkyl); (b) -(C2-to-C6-alkenyl);
(c) halogen;
(d) -(CH2)mNR8R9, where m is zero-to-six, and NR8R9 is either a nitrogen atom attached to R8 and R9, wherein R8 and R9 are independently selected from the group consisting of:
(1) hydrogen;
(2) -R400, where R400 is selected from the group consisting of: a. mod-aryl, as defined below, wherein the one, two, or three substituents, each designated R302, are independently selected from the group consisting of:
1. -(Ci-to-Cy-alkyl);
2. -(C2-to-C6-alkenyl);
3. halogen;
4. -(CH2)mNRl8Rl9? W ere m is as defined above and NR18R19 is either a nitrogen atom attached to R18 and R19, wherein Rl» and R*9 are independently selected from the group consisting of hydrogen, -(Ci- C6-alkyl), unsubstituted aryl-, and unsubstituted aryl-(Cι-C6-alkyl); or NR!8R19 may be a 3-to- 7-membered heterocyclic ring comprising ring carbon atoms, the nitrogen atom shown, and zero, one or two additional heteroatoms independently selected from the group consisting of -O-, -NH-, -N(Cι-to-C6-alkyl) and -S(O)s-, wherein s is zero, one or two;
5. -CN;
6. -CHO;
7. mono-, di-, tri-, or perhalogenated
-C1-C6- alkyl, as defined below; 8. -S(O)sR18, where s and R18 are as defined above;
9. -C(O)NR18R19, where NR18R19 is as defined above;
10. -(CH2)mOR18, where m and R18 are as defined above;
11. -CH(OR16)(OR17), where R16 and R17 are independently chosen from -(Cι-to-C3 alkyl) or, taken together, R16 and R17 form an ethylene or propylene bridge;
12. -(CH2)mOC(O)R18, where m and R18 are as defined above;
13. -(CH2)mC(O)OR18, where m and R18 are as defined above;
14. -OR10, where R10 is: (i) -PO(OH)O-M+, wherein M+ is a proton or a positively charged inorganic or organic counterion, as defined below, (ii) -SO3"M+, wherein M+ is as defined above, (iii) -C(O)(CH2)mC(O)O-M+, wherein m and M+ are as defined above;
15. -NO2;
16. -N3;
17. -(C -to-C6-alkynyl);
18. -C≡C-Si(CH3)3; and
19. guanidino substituted by hydrogen; -(Cι-C6-alkyl); unsubstituted aryl; (Cι-C8-alkyl)-C(O); unsubstituted aryl-S(O)2; (Ci-C6-alkyl)-OC(O)-; unsubstituted aryl-(Cι-C6-alkyl)- OC(O); unsubstituted aryl-OC(O); or (Ci-C6-alkyl)-SO2-; or taken together, any two adjacent R302 substituents in a di- or trisubstituted mod-aryl group form a 5-, 6- or 7- membered carbocyclic ring or a 5-, 6- or 7-membered heterocyclic ring wherein " the ring atoms consist of carbon atoms and one or two heteroatoms independently selected from the group consisting of -O-, -S(O)s-, where s is as defined above, and -NR18-, where R18 is as defined above; b. -Q-mod-aryl, where mod-aryl is as defined below and substituent(s) R^02 is/are as defined above, and the divalent radical -Q- is selected from the group consisting of:
1. -(Ci-to-Ce-alkyl)-;
2. -(C2-to-C6-alkenyl)-;
3. -(C2-to-C6-alkynyl)-;
4. -(CH2)mO-, wherein m is as defined above;
5. -O(CH )m-, wherein m is as defined above;
6. -N(R18)C(O)-, wherein R 8 is as defined above;
7. -C(O)N(R18)-, wherein R18 is as defined above;
8. -S(O)s-, wherein s is as defined above;
9. -N(R18)-, wherein R18 is as defined above;
10. -N(R18)S(O)r, wherein t is one or two, and R18 is as defined above;
11. -S(O)tN(R18)-, wherein t and R18 are as defined above;
12. -C(O)-;
13. -NN-;
14. -CHN-;
15. -NCH-;
16. -ONCH-; and
17. -CHNO-; c. -mod-Het, as defined below, wherein the one, two, or three substituents, each designated R302, are independently selected, and are as defined above; d. -Q-mod-Het, where Q is as defined above; e. -biaryl, as defined below; f. -Q-biaryl, where Q is as defined above; g. -mod-aryl-Q-mod-aryl, where Q is as defined above; h. -mod-aryl-Q-mod-Het, where Q is as defined above; i. -mod-Het-Q-mod-aryl, where Q is as defined above; j. -mod-Het-Q-mod-Het, where Q is as defined above; k. -mod-Het-mod-aryl; 1. -mod-aryl-mod-Het; and m. -mod-Het-mod-Het;
(3) -(d-to- -alkyl);
(4) substituted-Cι-to-C6-alkyl, as defined below;
(5) -(C3-to-C6-alkenyl);
(6) substituted-C3-to-C6-alkenyl, as defined below;
(7) -(C3-to-C6-alkynyl);
(8) substituted-C3-to-C6-alkynyl, as defined below;
(9) -(cyclo-C3-to-Cιo-alkyl);
(10) substituted-cyclo-C3-to-Cιo-alkyl, as defined below;
(11) -(cyclo-C4-to-Cιo-alkenyl);
(12) substitu_ed-cyclo-C4-to-Cιo-alkenyl, as defined below;
(13) -(bicyclo-C6-to-Cιo-alkyl);
(14) substituted-bicyclo-C6-to-Cιo- alkyl, as defined below;
(15) -(bicyclo-C6-to-Cιo-a_kenyl);
(16) substituted-bicyclo-C6-to-Cιo-alkenyl, as defined below;
(17) -(bicyclo-C6-to-Cιo-alkenyl)-Cι-to-C6-alkyl; and (18) substituted-bicyclo-C6-to-Cιo-alkenyl-Cι-to-C6- alkyl, as defined below; or -NR8R9 may be a 3- to 7-membered heterocyclic ring, where the ring consists of carbon atoms, the nitrogen atom shown, and zero, one or two additional heteroatoms independendy selected from the group consisting of -O-, -S(O)s-, wherein s is as defined above, and -NR8-, wherein R8 is as defined above;
(e) -CN;
(f) -CHO;
(g) mono-, di-, tri-, or perhalogenated -Ci-Cg-alkyl; (h) -S(O)sR8, where s and R8 are as defined above; (i) -C(O)NR8R9, where NR8R9 is as defined above;
(j) -(CH2)mOR8, where m and R8 are as defined above; (k) -CH(OR16)(OR17), where R^ and R17 are as defined above; (1) -(CH2)mOC(O)R8, where m and R8 are as defined above; (m) -(CH2)mC(O)OR8, where m and R8 are as defined above; (n) -OR10, where R10 is as defined above; (o) -NO2;
(P) -N3;
(q) -R400, as defined above;
(r) -S(O)tNR8R9, where t and NR8R9 are as defined above; (s) -NR8S(O)tR9, where t, R8 and R9 are as defined above; (t) -(C2-to-C6-alkynyl); (u) -C≡C-Si(CH3)3; and
(v) guanidino substituted by hydrogen; -(Cι-C6-alkyl); -mod- aryl; (Cι-C8-alkyl)-C(O)-; mod-aryl-SO2-; (Ci-Cfc-alkyl)- OC(O)-; mod-aryl-(Cι-C6-alkyl)-OC(O); mod-aryl- OC(O)-; or (Cι-C6-alkyl)Sθ2-;or taken together, any two adjacent R301 substituents in a di- or trisubstituted aryl group form a 5-, 6- or 7-membered carbocyclic ring or a 5-, 6- or 7-membered heterocyclic ring wherein the ring atoms consist of carbon atoms and zero, one or two heteroatoms independently selected from the group consisting of -O-, -S(O)s-, where s is as defined above, and -NR8-, where R8 is as defined above; with the proviso that each R301 substituent or each ring formed by two adjacent R301 groups may comprise no more than twenty non- hydrogen atoms;
(v) aryl-, as defined below and substituent(s) R301 is/are as defined above;
(vi) Het-, as defined below;
(vii) heterocyclic-, as defined below;
(viii) mono-, di-, tri-, or per-halogenated-Ci-Cό-alkyl-;
(ix) -(cyclo-C5-Cιo-alkenyl);
(x) -(cyclo-C5-Cιo-alkenyl-Cι-C3-alkyl);
(xi) -(bicyclo-C6-Ci2-alkenyl);
(xii) -(bicyclo-C6-Cι2-alkenyl-Cι-C3-alkyl); (C) -NR14R15, wherein NR14R15 is either a nitrogen atom attached to R14 and R15, wherein R14 and R15 are independently selected from the group consisting of:
(i) hydrogen;
(ii) -R400 5 as defined above;
(iii) -(Cι-to-Cιo-alkyl);
(iv) sub-Cι-to-Cιo-alkyl, as defined below;
(v) -(cyclo-C3-to-Cιo-alkyl);
(vi) sub-cyclo-C3-to-Cιo-alkyl, as defined below;
(vii) -(cyclo-C3-to-Cιo-alkyl-Cι-to-C3-alkyl);
(viii) sub-cyclo-C3-to-Cιo-alkyl-Cι-to-C3-alkyl, as defined below;
(ix) -(C3-to-Cιo-alkenyl);
(x) sub-C3-to-Cιo-alkenyl, as defined below;
(xi) -(cyclo-C4-to-Cιo-alkenyl);
(xii) sub-cyclo- -to-Cio-alkenyl, as defined below;
(xiii) -(cyclo-C6-to-Cιo-alkyl-C3-C5-alkenyl);
(xiv) sub-cyclo-C6-to-Cιo-alkyl-C3-C5-alkenyl, as defined below;
(xv) -(C3-to-Cιo-alkynyl);
(xvi) sub-C3-to-Cιo-alkynyl, as defined below;
(xvii) -(cyclo- -_o-Cιo-alkyl-C3-C5-alkynyl);
(xviii) sub-cyclo-C6-to-Cιo-alkyl-C3-C5-alkynyl, as defined below;
(xix) -(bicyclo-Cό-to-Cio-alkyl);
(xx) sub-bicyclo-C6-to-Cιo-alkyl, as defined below;
(xxi) -(bicyclo-C6-to-Cιo-alkenyl);
(xxii) sub-bicyclo-C6-to-Cιo-alkenyl, as defined below;
(xxiii) -aryl; (xxiv) -Het; and
(xxv) R6, where R6 is selected from the group consisting of:
(a) hydrogen;
(b) -(Cι-to-Cιo-alkyl);
(c) mod-Ci-to-Cio-alkyl, as defined below;
(d) -(C3-to-Cιo-alkenyl);
(e) mod-C3-to-Cιo-alkenyl, as defined below;
(f) -(C3-to-Cι0 alkynyl);
(g) mod-C3-to-Cιo-alkynyl, as defined below; (h) -(cyclo-C3-to-Cιo-alkyl);
(i) mod-cyclo-C3-to-Cιo-alkyl, as defined below; (j) -(cyclo-C4-to-Cιo-alkenyl); (k) mod-cyclo-C4-to-Cιo-alkenyl, as defined below; (1) -(bicyclo-C6-to-Cιo-alkyl); (m) mod-bicyclo-C6-to-Cιo-alkyl, as defined below; (n) -(bicyclo-C6-to-Cιo-alkenyl); (o) mod-bicyclo-C6-to-Cιo-alkenyl, as defined below; (p) -R8, as defined above; (q) -aryl; and (r) -Het; or -NR1 R15 may be a 3- to 7-membered heterocyclic ring, where the ring consists of carbon atoms, the nitrogen atom shown, and zero, one or two additional heteroatoms independently selected from -O-, -S(O)s-, wherein s is as defined above, and -NR8-, wherein R8 is as defined above, which ring is unsubstituted or substituted with from one-to-five compatible radicals independently selected from the group consisting of: (i) R6, as defined above;
(ii) -(CH2)π,OR6,where m and R6 are as defined above; (iii) -(CH2)mNR6R7, where m is as defined above and NR6R7 is either a nitrogen atom attached to R6 and R7, wherein R6 is as defined above and R7 is independently selected from the group defining R6, or
-NR6R7 may be a 3- to 7-membered heterocyclic ring, where the ring consists of carbon atoms, the nitrogen atom shown, and zero, one, or two additional heteroatoms independently selected from the group consisting of -O-, -S(O)s-, wherein s is as defined above, and -NR8-, wherein R8 is as defined above, which ring is unsubstituted or substituted with from one-to-six compatible radicals independently selected from the group consisting of:
(a) -R8, as defined above;
(b) -(CH2)π,OR8, wherein m and R8 are as defined above;
(c) -S(O)sR8, wherein s and R8 are as defined above; .
(d) -S(O)tNR8R9, wherein t and NR8R9 are as defined above;
(e) -(CH2)mNR8R9, wherein m and NR8R9 are as defined above;
(f) -SO3H;
(g) =NOR8, wherein R8 is as defined above; (h) -R400, as defined above;
(i) -aryl; (j) -Het; and
(k) -R3", wherein R399 is selected from the group consisting of:
(1) hydroxyl;
(2) -C(O)OH;
(3) -C(O)OR8, where R8 is as defined above;
(4) -(cyclo-C3-.o-C7-a.kyl);
(5) oxo;
(6) thiooxo;
(7) epoxy;
(8) halogen;
(9) -CN;
(10) -N3;
(11) -NO2;
(12) -OR10, where R10 is as defined above;
(13) -S(O)tNR8R9, where t and NR R9 are as defined above;
(14) -NR8S(O)tR9, where t, R8 and R9 are as defined above;
(15) -CH(OR16)(OR17), where R^ and R17 are as defined above; and
(16) guanidino substituted by hydrogen, -(Ci- - alkyl); aryl; (Ci- -alky^CO-; aryl-SO2-; (Ci- C6-a-kyl)OC(O)-; aryl-(Cι-C6-alkyl)OC(O)-; aryl-OC(O)-; or (Cι-C6-alkyl)-SO2-; (iv) -C(O)OR6, where R6 is as defined above;
(v) -SO3H;
(vi) -S(O)sR6, where s and R6 are as defined above;
(vii) -S(O)tNR6R7, where t and NR6R7 are as defined above;
(viϋ) =NOR6, where R6 is as defined above;
(ix) -aryl;
(x) -Het;
(xi) -R399, as defined above; and
(xii) -R400, as defined above;
(D) -aryl;
(E) Het-;
(F) mono-, di-, tri-, or per-halogenated-Cι-C6alkyl;
(G) -N(R8)NR14R15, where R8 and NR14R15 are as defined above;
(H) -Si(Rn)3, where each R11 is independently -(Ci-Cβ-alkyl), aryl-(Cι-C6- alkyl)-, or aryl;
(I) -OSi(R11)3, where each R11 is independently as defined above;
(J) -Sn(R )3, where each R11 is independently as defined above;
(K) -PO .11^, where each R11 is independently as defined above;
(L) -R14, where R14 is as defined above; or
(M) halogen; (II) -O(CH2)mS(O)sR12, where m, s and R12 are as defined above; (HI) -O(CH2)jCN, where j is as defined above; (TV) -O(CH2)jC(=NOR14)R12, where j, R12 and R14 are as defined above;
(V) -O(CH2)jC(=N+(O-)R14)R12, where j, R12 and R14 are as defined above, with the proviso that R14 may not be hydrogen;
(VI) -O(CH2)jC(=NOR14)R15, where j, R14 and R^ are as defined above;
(Vπ) -O(CH2)jC(=N+(O-)R14)R15, where j, R14 and R15 are as defined above, with the proviso that R14 may not be hydrogen; (Vπi) -OC(O)O(CH2)jC(O)NR14R15, where j and NR14R15 are as defined above; (K) -O(CH2)jNR6C(O)OR14, where j, R6 and R14 are as defined above;
(X) -O(CH2)jNR6C(O)NR14R15, where j, R6 and NR14Ri5 are as defined above;
(XI) -O(CH2)jNR6C(O)NR NR14R15, where j, R6, R7 and NR14R15 are as defined above;
(XII) -O(CH2)jNR6C(O)R14, where j, R6 and R14 are as defined above; and (Xπi) -O(CH2)jNR6C(O)OC(O)R14, where j, R6 and R14 are as defined above; R2 and R2a are independently hydrogen, halogen, or -OR14, wherein R14 is as defined above, or one of R2 and R2*1 may be hydroxy, when the other of R2 or R21 is hydrogen, or R2 and R23 taken together is oxo or thiooxo;
R3 and R4 are chosen, when R5 is hydrogen, such that one of R3 and R4 is hydrogen and the other is selected from hydrogen, hydroxy, -OCOR8, where R8 is as defined above, or -OSi(R11)3, where each R11 is independently as defined above, or one of R3 and R4 is joined with non-hydrogen R5 to form a C-23/C-24 bond, with the other being hydrogen, hydroxy, -OCOR8, where R8 is as defined above, or -OSi(R11)3, where each R11 is independently as defined above;
R5 is hydrogen, or taken together with either R3 or R4, forms a C-23/C-24 bond.
The compounds of the invention are subject to the proviso that, when R2 and R2a are both hydrogen and Rla is methyloxy, then it is understood that R1 may not be defined as, (I)-O(CH2)jC(O)R20, where j is as defined above and R20 is selected from
(A) hydroxy;
(B) -OR21 wherein R21 is loweralkyl, cycloalkyl, cycloalkylalkyl or qualified- arylalkyl, where qualified-arylalkyl is defined below; and
(C) -NR22R23, wherein NR22R23 is either: a nitrogen atom attached to R22 and R23, where R22 is selected from hydrogen, loweralkyl, qualified-arylalkyl, cycloalkyl and cycloalkylalkyl; and R23 is selected from hydrogen, loweralkyl, qualified-arylalkyl, cycloalkyl, cycloalkylalkyl, aminoalkyl, hydroxyalkyl, carboxyalkyl, and thioloweralkyl; or a saturated heterocyclic ring, where taken together, R22 and R23 are
-(CH2)q- wherein q is two to five; or is morpholino; or (II) -O(CH2)jC(O)N(R )(CH2)mCH(R25)C(O)R20, where j, m and R20 are as defined above and R24 is selected from hydrogen, loweralkyl, qualified-arylalkyl, cycloalkyl and cycloalkylalkyl; and R25 is selected from hydrogen, loweralkyl, hydroxyloweralkyl, carboxyalkyl, thioloweralkyl, thioalkoxyalkyl, guanidinoalkyl, aminoalkyl, qualified-arylalkyl and, if m is other than zero, amino or amidoalkyl; or taken together, R24 and R25 are -(CH2)p-, wherein p is two to five; or (πi) -O(CH2)jC(O)N(R2 )(CH2)mCH(R25)-C(O)N(R 6)(CH2)mιCH(R27)-C(O)R20, where j, m, R20, R24 and R25 are as defined above, and ml is zero to six, R26 is selected from hydrogen, loweralkyl, qualified-arylalkyl, cycloalkyl and cycloalkylalkyl; and R27 is selected from hydrogen, loweralkyl, hydroxyloweralkyl, carboxyalkyl, thioloweralkyl, thioalkoxyalkyl, guanidinoalkyl, aminoalkyl, qualified-arylalkyl and, if ml is other than zero, amino or amidoalkyl; or taken together, R26 and R27 are -(CH2)p-, wherein p is as defined above; or (IY) -O(CH2)jC(O)N(R24)(CH2)mCH(R 5)-C(O)N(R 6)(CH2)mιCH(R27)-
C(O)N(R28)(CH2)m2CH(R29)C(O)R20,where j, m, ml, R20, R24, R25, R^ and R27 are as defined above, and m2 is zero to six, R28 is selected from hydrogen, loweralkyl, qualified-arylalkyl, cycloalkyl and cycloalkylalkyl; and R29 is selected from hydrogen, loweralkyl, hydroxyloweralkyl, carboxyalkyl, thioloweralkyl, thioalkoxyalkyl, guanidinoalkyl, aminoalkyl, qualified-arylalkyl and, if m2 is other than zero, amino or amidoalkyl; or taken together, R28 and R29 are -(CH )p-, wherein p is as defined above.
It is understood that when a variable, such as m, s, t, M+, Q, R6, R7, R8, R9, R10, R11, R 3, R14, Ri5, R16, RI7, R18, R19, R301? R302? R399, R400, ^^ a]kenylϊ alkynyl aryl> Het> mod-aryl, mod-Het, or the like, occurs more than once in a formula, its value is chosen independently at each occurance. It is further understood that the present application is not claiming substituents or substitution patterns that are impractical or unreasonable to prepare.
Preferred compounds according to the present invention are represented by formula (II):
wherein n, R, R2, R23, R3, R4 and R5 are as defined above and A is selected from among: , where j, R12,
R13, R14 and R15 are as defined above.
More preferred compounds according to the present invention are represented by formula (III):
wherein n, R, R2, R2a, R3, R4 and R5 are as defined above and B is selected from:
where j, m, R6, R14 and R15 are as defined above, and aryl is as defined below.
Most preferred compounds according to the present invention are represented by formula (TV):
wherein n, R, R2, R2 , R3, R4 and R5 are as defined above and D is selected from:
above.
Preferred compounds according to the invention are the compounds of:
Formula II, wherein R= ethyl; n= 1; R2=R2a__.R3=R5=H; R4=0H; and A=-OCH2C(O)-O- CH2-[(lR)-(+)-alpha-pinen-10-yl)];
Formula II, wherein R= ethyl; n= 1; and A=- OCH2C(O)-O-CH2-[(lR)-(+)-a-pinen-10-yl)]; Formula II, wherein R= ethyl; n= 1; R4=OH; and A=-OCH2C(O)-O- CH2-(4-nitrophenyl);
Formula II, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R =OH; and A= -OCH2C(O)OC2H5;
Formula II, wherein R= ethyl; n= 1; R =R2a=R3=R5-=H; R4=0H; and A= -OCH2C(O)OCH2C6H5;
Formula II, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=0H; and A= -OCH2C(O)OH;
Formula II, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=0H; and A= -OCH2C(O)OCH2-(9-fluorenyl);
Formula II, wherein R= ethyl; n= 1; R2=R2a__.R3=H; A= -OCH2C(O)OCH2Ph; and R4 and R5 taken together form a bond; and
Formula II, wherein R= ethyl; n= 1; R2=R a=R3=R4:=R5=H; and A= -OCH2C(O)OH;
Formula II: R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=0H; A= -OCH2C(O)OCH2CCl3;
More preferred compounds according to the invention are the compounds of:
Formula m, wherein R= ethyl; n= 1; R2=R2a__.R3=R5=H; R4=0H; and B= -OCH2C(O)- NHR^, where R15=_-CH(CH3)CONHCH(CH3)CONHCH(CH3)CO2H (all chiral centers in Rl5 are R configuration);
Formula in, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=0H; and B= -OCH2C(O)- N(CH2CH2N(CH3)(CH2CH2OH))-phenyl;
Formula m, wherein R= ethyl; n= 1; R2=R a=R3=R5=H; R4=0H; and B= -OCH2C(O)- N(CH2CH2N(CH3)2)-phenyl;
Formula IE, wherein R= ethyl; n= 1; R2_=R2a=R3=R5=H; R4=0H; and B= -OCH2C(O)- NHNHCO2CH3;
Formula IE, wherein R= ethyl; n= 1; R2=R a= 3=R5--:H; R4=0H; and B= -OCH2C(O)- N(CH2CH2OH)-NHCO2CH3; Formula m, wherein R= ethyl; n= 1; R =R2a_= 3=R5=H; R4=0H; and B= -OCH2C(O)- N(CH2CH2CH2θCOCH2CH2Cθ2H)(4-fluorophenyl);
Formula IE, wherein R= ethyl; n= 1; R2=R a= 3= 5=H; R4=0H; and B= -OCH2C(O)- HN(CH2)5NH-dansyl;
Formula IE, wherein R= ethyl; n= 1; R2=R2a__.R3_=R5_=H; R4=0H; and B= -OCH2C(O)N(phenyl)CH2CH2CH2OH; and
Formula IE, wherein R= ethyl; n= 1; R2=R a=R3=R5=H; R4=0H; and B=-OCH2C(O)- NH(6-carbomethoxymethy_mercaptopurine hydrazidyl);
Most preferred compounds according to the invention are the compounds of:
Formula IV, wherein R= ethyl; n= 1; R2_=R2a= 3=R5=H; R4=OH; and D= -OCH2C(O)- NH-benzyl;
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R =OH; and D= -OCH2C(O)- N(CH3)-benzyl;
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=0H; and D= -OCH2C(O)- NH2;
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3__,R5=H; R4=0H; and D= -OCH2C(O)- NH-CH3;
Formula IV, wherein R= ethyl; n= 1; R2=R a_=R3_=R5=H; R4=0H; and D= -OCH2C(O)-
N(CH3)2;
Formula IV, wherein R= ethyl; n= 1; R =R2a=R3= 5=H; R4=0H; and D= -OCH2C(O)- NH-ethyl;
Formula IV, wherein R= ethyl; n= 1; R2=R2a= 3=R5=H; R4=0H; and D= -OCH2C(O)- N(CH )-ethyl;
Formula IV, wherein R= ethyl; n= 1; R2_=R2a= 3=R5-=H; R4=0H; and D= -OCH2C(O)- NH-CH2CH2CH3; Formula IV, wherein R= ethyl; n= 1; R =R2a=R3=R5=H; R4=0H; and D= -OCH2C(O)- N(CH3)-CH2CH2CH3;
Formula IV, wherein R= ethyl; n= 1; R =R2a=R3=R5=H; R4=0H; and D= -OCH2C(O)- NH-CH(CH3)2;
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=0H; and D= -OCH2C(O)- N(CH3)-CH(CH3)2;
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=0H; and D= -OCH2C(O)- NH-cyclopropyl;
Formula IV, wherein R= ethyl; n= 1; R2=R2a= 3= 5=H; R4=0H; and D= -OCH2C(O)- NH-CH2CH2CH2CH3;
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=0H; and D= -OCH2C(O)- N(CH3)-CH2CH2CH2CH3;
Formula IV, wherein R= ethyl; n= 1; R2=R a=R3=R5_=H; R4=0H; and D= -OCH2C(O)- NH-CH2CH(CH3)2;
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3=R5_=H; R4=0H; and D= -OCH2C(O)- N(CH3)-CH2CH(CH3);
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=0H; and B= -OCH2C(O)- NHNH-CO-(4-pyridyl);
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=0H; and D= -OCH2C(O)- NH-cyclobutyl;
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3__.R5=H; R4=0H; and D= -OCH2C(O)- NH-CH2CH2CH2CH2CH3;
Formula IV, wherein R= ethyl; n= 1; R =R2a=R3=R5=H; R4=0H; and D= -OCH2C(O)- N(CH3)-CH2CH2CH2CH2CH3; Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=θH; and D= -OCH2C(O)- NH-CH2CH2CH(CH3)2;
Formula IV, wherein R= ethyl; n= 1; R^R^ ^R^H; R4=0H; and D= -OCH2C(O)- N(CH3)-CH2CH2CH(CH3)2;
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=0H; and D= -OCH2C(O)- NH-cyclopentyl;
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4_=0H; and D= -OCH2C(O)- NH-CH2CH2CH2CH2CH2CH3;
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=0H; and D= -OCH2C(O)- N(CH3)-CH2CH2CH2CH2CH2CH3;
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H. R4=0H; and D= -OCH2C(O)- NH-cyclohexyl;
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3=R5=-H; R4=OH; and D= -OCH2C(O)- NR6R7, where R6 and R7> taken together= -CH2CH2OCH2CH2-, thus forming a six- membered ring incorporating the nitrogen to which they are attached;
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=0H; and B= -OCH2C(O)- NH(4-morpholinyl) ;
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=0H; and D= -OCH2C(O)- NH-CH2CH2OH;
Formula IV, wherein R= ethyl; n= 1; R2=R2 =R3=R5=H; R4=0H; and D= -OCH2C(O)- NH-CH2CH2CH2OH;
Formula IV, wherein R= ethyl; n= 1; R2-=R2a=R3=R5=H; R4=OH; and D= -OCH2C(O)- NH-CH2CH2CH2CH2OH;
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=0H; and D= -OCH2C(O)- NH-CH2CH2CH2CH2CH2OH; Formula IV, wherein R= ethyl; n= 1; R2=R a=R3=R5=H; R4=QH; and D= -OCH2C(O)- NH-CH2CH2NH2;
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3=R5-=H; R4=OH; and D= -OCH2C(O)- NH-CH2CH2CH2NH2;
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=0H; and D= -OCH2C(O)- NH-CH2CH2CH2CH2NH2;
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=0H; and D= -OCH2C(O)- NH-CH2CH2CH2CH2CH2NH2;
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=0H; and D= -OCH2C(O)- NH-CH2CO2CH2Ph;
Formula IV, wherein R= ethyl; n= 1; R =R2a=R3=R5=H; R4=0H; and D= -OCH2C(O)- NH-CH2CO2H;
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=0H; and D= _oCH2C(O)- NH-CH2CH2CO2CH2Ph;
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=0H; and D= -OCH2C(O)- NH-CH2CH2CO2H;
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=0H; and D= -OCH2C(O)- NH-(R)-CH(CH3)CO2H, and has anR configuration;
Formula IV, wherein R= ethyl; n= 1; R =R2a=R3=R5=H; R4=0H; and D= -OCH2C(O)- NH-(S)-CH(CH3)CO2H;
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=0H; and D= -OCH2C(O)- NH-3-phenyl-phenyl;
Formula IV, wherein R= ethyl; n= 1; R2=R2a__:R3=R5-=H; R4=0H; and D= -OCH2C(O)- N(CH2CH2OH)(3-phenyl-phenyl);
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=0H; and D= -OCH2C(O)-
N(CH2(3-pyridyl))2; Formula IV, wherein R= ethyl; n= 1; R =R a=R3=R5=H; R4=0H; and D= -OCH2C(O)-
N(cyclohexyl)2;
Formula IV, wherein R= ethyl; n= 1; R2_=R a=R3=R5=H; R4=0H; and D= -OCH2C(O)- NH(4-thiomorpholinyl);
Formula IV, wherein R= ethyl; n= 1; R =R2a=R3=R5=H; R4=0H; and D= -OCH2C(O)- NH(4-CF3-phenyl);
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3= 5=H; R4=0H; and D= -OCH2C(O)- NH(4-F-phenyl);
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3=R5=-H; R4=OH; and D= -OCH2C(O)- NH(4- (4-morpholino)-phenyl) ;
Formula IV, wherein R= ethyl; n= 1; R =R2a=R3__:R5=H; R4=OH; and D= -OCH2C(O)- NH(4-HO-phenyl);
Formula IV, wherein R= ethyl; n= 1; R =R2a=R3=R5=H; R4=0H; and D= -OCH2C(O)- NH-3-pyridyl;
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=0H; and D= -OCH2C(O)- NH-4-pyridyl;
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3__,R5=H; R4=0H; and D= -OCH2C(O)- NH-2-pyridyl;
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=0H; and D= -OCH2C(O)- N(CH3)-CH2CH2OH;
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=0H; and D= -OCH2C(O)-(L- prolinocarboxamide);
Formula IV, wherein R= ethyl; n= 1; R =R2a=R3= 5=H; R4=0H; and D= -OCH2C(O)-(D- prolinocarboxamide); Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=0H; and D= -OCH2C(O)-(L- prolinol);
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=0H; and D= -OCH2C(O)-(D- prolinol);
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3__:R5=H; R4=0H; and D= -OCH2C(O)- NH(3-(phenylethynyl)phenyl);
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3=R5:=H; R4=0H; and D= -OCH2C(O)- N(CH2CH2CH2OH)(4-fluorophenyl);
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=OH; and D= -OCH2C(O)NR6R7, where R6 and R7, taken together, form the diradical, -CH2CH2- C(OCH2CH2O)CH2CH2-;
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=OH; and D= -OCH2C(O)- NH(3-fluorophenyl);
Formula IY, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=OH; and D= -OCH2C(O)- NH(3-hydroxy-phenyl);
Formula IY, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=0H; and D= -OCH2C(O)NR6R7, where R6 and R7, taken together, form the diradical, -CH2CH2-NCH3- CH2CH2-;
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=OH; and D= -OCH2C(O)- NH{ 6-( 1 ,4-benzodioxanyl) } ;
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R =R5=H; R4=OH; and D= -OCH2C(O)- NH(3 ,4-methylenedioxy-phenyl) ;
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R =R5=H; R4=OH; and D= -OCH2C(O)- NH- 1 -naphthalenyl;
Formula IV, wherein R= ethyl; n= 1; R2=R2a__.R3=R5=H; R4=0H; D= -OCH2C(O)R12; and R12 = NR6R7; where R6 and R7 taken together = -CH2CH2CH2CH2-, thus forming a five membered ring incorporating the nitrogen to which they are attached; Formula IV, wherein R= ethyl; n= 1; R2=R2a= 3=R5=H; R4_=OH; D= -OCH2C(O)R12; and R12 _ NR6R7; where R6 and R7 taken together = -CH2CH2CH2CH2CH2-, thus forming a six membered ring incorporating the nitrogen to which they are attached;
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3=R5=-H; R4=0H; and D= -OCH2- C(O)NH-CH2CH2C6H5;
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=0H; and D= -OCH2- C(O)N(CH3)-CH2CH2C6H5;
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=0H; and D= -OCH2-C(0)- NHC6H5;
Formula IV, wherein R= ethyl; n= 1; R2=R2a__:R3=R5=H; R4=0H; and D= -OCH2- C(O)-NH(CH2)2N(CH2CH2)2O;
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=OH; and D= -OCH2- C(O)-NH(CH2)3N(CH2CH2)2O;
Formula IV, wherein R= ethyl; n= 1; R =R2a__.R3=R5=H; R4=0H; and D= -OCH2- C(O)-NH(CH2)2N(CH3)2;
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3__.R5=H; R4=0H; and D= -OCH2- C(O)-NH(CH2)3N(CH3)2;
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3_=R5=H; R4=OH; and D= -OCE_2-C(O)- (S)-NHCH(CH2C6H5)CO2CH2Ph;
Formula IV, wherein R= ethyl; n= 1; R =R2a_=R3=R5=H; R4=OH; and D= -OCH2-C(O)- (5)-NHCH(CH2C6H5)CO2H;
Formula IV, wherein R= ethyl; n= 1; R2=R2a= 3=R5__:H; R4=0H; and D= -OCH2-C(O)- (R)-NHCH(CH2C6H5)CO2CH2Ph;
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3_=R5=H; R4=θH; and D= -OCH2-C(O)- (R)-NHCH(CH2C6H5)CO2H; Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=OH; and D= -OCH2- C(O)-HN(CH2)2SH;
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=0H; and D= -OCH2-C(O)- HN(CH2)3SH;
Formula IV, wherein R= ethyl; n= 1; R2_=R2a=.R3=R5=H; R4=0H; and D= -OCH2C(O)- NH-2-naphthyl;
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3=R4=R5=H; and D= -OCH2C(O)-NR6R7, where R6 and R7, taken together, are the diradical, -CH2CH2OCH2CH2-;
Formula IV, wherein R= ethyl; n= 1; R2_=R2a=R3=R5=H; R4=0H; and D= -OCH2C(O)- NH { 4-(H2NS O2)-phenyl } ;
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3__:R5-=H; R4=OH; and D= -OCH2C(O)NR6R7, where R6 and R7, taken together, form the diradical, -CH2CH2- N(CH2CH2OH)CH2CH2-;
Formula IN, wherein R= ethyl; n= 1; R2=R2a_=R3=R5=H; R4=0H; and D= -OCH2C(O)- Ν(CH3)phenyl;
Formula IV, wherein R= ethyl; n= 1; R2__:R2a__:R3=R5=H. R4=0H; and D= -OCH2C(O)- N(CH2CH2OH)2;
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R =OH; and D= -OCH2C(O)- N(CH3)CH2CH2CH2N(CH3)2;
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3=R5__.H; R4=OH; and D= -OCH2C(O)- NH-CH(CH2OH)2;
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=0H; and D= -OCH2C(O)-
NH{3-(CF3)-phenyl};
Formula IV, wherein R= ethyl; n= 1; R2=R2a-=R3=R5=H; R4=0H; and D= -OCH2C(O)-
N(CH2CN) ; Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=OH; and D= -OCH2- C(O)NR6R7, where R6 and R7, taken together, form the diradical, -CH2CH2-;
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4_=0H; and D= OCH2- NH(CO)NR6R7; where R6 and R7, taken together, are the diradical, -CH2CH2OCH2CH2-;
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3-_:R5==H; R4=0H; and D= OCH2- NH(CO)NH-phenyl;
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=0H; and D= OCH2- NH(CO)NH-CH2CH2CH2OH;
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=0H; and D=OCH2C(O)- NR6R7, where R6 and R7, taken together, form the diradical, -CH2CH2SO2CH2CH2-;
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=0H; and D= OCH2C(O)-NH- CH2CH2-(4-F-phenyl);
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3= 5=H; R4=0H; and D= OCH2C(O)- NH(4-Cl-phenyl);
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=0H; and D= OCH2C(O)- NH(4-(OCH3)-phenyl);
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=0H; and D= OCH2C(O)- NH(4-CH3-phenyl);
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R =R5=H; R4=QH; and D= OCH2C(O)- NH(3,4-Cl2-phenyl);
Formula IV, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=0H; and D= OCH2C(O)- NH(3-I-phenyl);
Formula IV, wherein R= ethyl; n= 1; R2-=R2a=R3=H; R4 and R5? \akeτι together, form a bond; and D=-OCH2C(O){4-(morpholinyl)};
Formula IV, wherein R= ethyl; n= 1; R2=R3=R5=H; R2a=R4 =0H; and D= OCH2- C(O)NH(3-fluoro-phenyl); and Formula IV: R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=OH; D= -OCH2C(O)NR6R7; R6_^ (CH2)2N(CH2CH2)2O; R7=-CH2CH2OH.
As used throughout this Specification and Claims, the following terms have the meanings specified:
"Acyl", as used herein, refers to an aryl or alkyl group, as defined below, appended to the remainder of the molecule via a carbonyl group. Examples include, but are not limited to, acetyl, pivaloyl, benzoyl, and the like.
"Acylamino" refers to an acyl group, as defined above, except that it is appended to the remainder of the molecule via an amino group. Examples include, but are not limited to, acetylamino, pivaloylamino, benzoylamino, and the like.
"Acylguanidino" refers to an acyl group, as defined above, except that it is attached to the remainder of the molecule via a nitrogen of a guanidino radical in one of three ways: HN(acyl)C(NH)NH- or H2NC(NH)N(acyl)- or (acyl)NC(NH2)HN-.
"Alkenyl" refers to straight- or branched-chain groups of a specified number of carbon atoms containing at least one carbon-carbon double bond including, but not limited to ethenyl, 1-propenyl, 2-propenyl, 2-methyl-l-propenyl, 1-butenyl, 2-butenyl, and the like.
"Alkoxy", "alkylether" and "loweralkoxy" refer to an alkyl group, as defined below, attached to the remainder of the molecule through an oxygen atom. Examples include, but are not limited to, methoxy, ethoxy, isopropoxy, n-butoxy, sec-butoxy, isobutoxy, tert-butoxy and the like.
"Alkoxycarbonyl" refers to an alkoxy group, as defined above, except that it is attached to the remainder of the molecule via a carbonyl group. Examples include, but are not limited to, methyloxycarbonyl, ethyloxycarbonyl, tert-butyloxycarbonyl, cyclohexyloxycarbonyl, and the like.
"Alkoxycarbonylamino" refers to an alkoxycarbonyl group, as defined above, except that it is attached to the remainder of the molecule via an amino group. Examples include, but are not limited to, methyloxy-carbonylamino, tert-butyloxycarbonylamino, and the like.
"Alkoxycarbonylguanidino" refers to an alkoxycarbonyl group, as defined above, except that it is attached to the remainder of the molecule via a nitrogen of a guanidino radical in one of three ways: HN(alkoxycarbonyl)C(NH)HN-, H2NC(NH)N(alkoxycarbonyl)- or (alkoxycarbθnyl)NC(NH2)HN-.
"Alkyl" refers to a straight- or branched-chain group of a specified number of carbon atoms including, as appropriate, but not necessarily limited to, methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, and the like. "Alkylamino" refers to a group having the structure -NH-(alkyl), where the alkyl portion is as defined above, including, for example, methylamino, ethylamino, isopropylamino, and the like.
"Alkylsulfonyl" refers to an alkyl group, as defined above, except that it is attached to the remainder of the molecule via a sulfur dioxide diradical. Examples include but are not limited to, methanesulfonyl, camphorsulfonyl and the like.
"Alkylthioether" and "thioalkoxy" refer to an alkyl group, as previously defined, except that it is attached to the remainder of the molecule via a sulfur atom. Examples include, but are not limited to, thiomethoxy, thioethoxy, thioisopropoxy, n-thiobutoxy, sec- thiobutoxy, isothiobutoxy, tert-thiobutoxy, and the like.
"Alkynyl" refers to straight- or branched-chain groups of a specified number of carbon atoms containing at least one carbon-carbon triple bond, including, but not limited to acetylenyl, propargyl, and the like.
"Amidoalkyl" refers to a group having the structure -NR1 1C(O)R102 appended to the remainder of the molecule via an alkyl group, as previously defined, wherein R101 and R102 are independently hydrogen, alkyl, aryl, arylalkyl, or halosubstituted alkyl, or R10l and R 02, taken together, may optionally be -(CH )aa-, where aa is an integer of from 2-to-6.
"Aminoalkyl" refers to a group having the structure -NR 03R104 appended to the remainder of the molecule via an alkyl group, as previously defined, wherein R103 and R104 are independently hydrogen, alkyl, qualified-aryl or qualified-arylalkyl, or Rl°3 and R104, taken together, may optionally be -(CH2)bb-, where bb is an integer of from 2-to-6.
"Aryl", as used herein, refers to mono-, di-, tri- or tetracyclic aromatic groups, charged or uncharged, the rings of which are comprised of from 3-to-7 carbon atoms. Examples of aryl include, but are not limited to, phenyl, 1- or 2-naphthyl, azulenyl, fluorenyl, (1, 2)-dihydronaphthyl, (l,2,3,4)-tetrahydronaphthyl, indenyl, indanyl and the like, which are unsubstituted or substituted with from one, two or three independently-selected substituents, R301, as defined above.
" Arylalkoxy" and "arylalkylether" refer to an arylalkyl group, as defined below, attached to the parent molecular moiety through an oxygen atom. Examples include, but are not limited to, benzyloxy, 2-phenethyloxy, 1-naphthylmethyloxy, and the like.
"Arylalkoxycarbonyl" refers to an arylalkoxy group, as defined above, except that it is attached to the remainder of the molecule via a carbonyl group. Examples include, but are not limited to, benzyloxycarbonyl, 9-fluorenylmethyloxycarbonyl, and the like.
"Arylalkoxycarbonylamino" refers to an arylalkoxycarbonyl group, as defined above, except that it is attached to the remainder of the molecule via an amino group. Examples include, but are not Umited to, benzyloxycarbonylamino, 9- fluorenylmethyloxycarbonylamino, and the like. "Arylalkoxycarbonylguanidino" refers to an arylalkoxycarbonyl group, as defined above, except that it is attached to the remainder of the molecule via a nitrogen of a guanidino radical in one of three ways: HN(arylalkoxycarbonyl)C(NH)HN-, H2NC(NH)N(arylalkoxycarbonyl)- or (arylalkoxycarbonyl)NC(NH2)HN-.
"Arylalkyl" refers to an aryl group, as previously defined, except that it is attached to the remainder of the molecule via an alkyl group.
"Arylalkylamino" refers to a group having the structure -NH- (arylalkyl), where the arylalkyl portion is as previously defined, except that it is attached to the remainder of the molecule via an amino group. Examples include benzylamino, 1-phenylethylamino, and the like.
"Arylalkylthioether" and "thioarylalkoxy" refer to an arylalkyl group, as previously defined, except that it is attached to the remainder of the molecule via a sulfur atom.
"Arylamino" refers to an aryl group, as defined above, except that it is attached to the remainder of the molecule via an amino group. Examples include, but are not limited to, anilino, naphthylamino, and the like.
"Arylether" and "aryloxy" refer to an aryl group, as previously defined, attached to the parent molecular moiety through an oxygen atom. Examples include, but are not limited to, phenoxy, 1-naphthoxy, 2-naphthoxy, and the like.
"Aryloxycarbonyl" refers to an aryloxygroup, as defined above, except that it is attached to the remainder of the molecule via a carbonyl group. Examples include, but are not limited to, phenyloxycarbonyl, and the like.
"Aryloxycarbonylamino" refers to an aryloxycarbonyl group, as defined above, except that it is attached to the remainder of the molecule via an amino group. Examples include, but are not Umited to, phenyloxycarbonylamino, and the like.
"Aryloxycarbonylguanidino" refers to an aryloxycarbonyl group, as defined above, except that it is attached to the remainder of the molecule via a nitrogen of a guanidino moiety in one of three ways: HN(aryloxycarbonyl)C(NH)HN-, H2NC(NH)N(aryloxycarbonyl)- or (aryloxycarbonyl)NC(NH2)HN-.
"Arylsulfonyl" refers to an aryl group, as defined above, except that it is attached to the remainder of the molecule via a sulfur dioxide group. Examples include, but are not limited to /?-toluenesulfonyl, benzenesulfonyl, and the like.
"Arylsulfonylguanidino" refers to an arylsulfonyl group, as defined above, except that it is attached to the remainder of the molecule via a guanidino group in one of three ways: HN(arylsulfonyl)C(NH)HN- or H2NC(NH)N(arylsulfonyl)- or (arylsulfonyl)NC(NH2)HN-.
"Arylthioether" and "thioaryloxy" refer to an aryl group, as defined above, except that it is attached to the remainder of the molecule via a sulfur atom. "Biaryl" refers to a mod-aryl group, as defined below, which carries as a substituent another independently selected mod-aryl group, such that the two are connected by a single carbon-carbon bond.
"Carboxamido" refers to an amino group attached to the remainder of the molecule via a carbonyl group, and having the formula H2NC(O)-.
" Carboxyalkyl" refers to a carboxyl group, -CO H, appended to the remainder of the molecule via an alkyl group, as previously defined.
" Counterion", as used herein, refers to a positively-charged atom or molecular species, with a net charge of +1, which includes, but is not limited to Li+, Na+, Ca(OC(O)CH3)+, MgCl+, K+, NH4 +, (n-butyl)4N+, and the like.
"Cycloalkenyl" refers to cyclic groups of 5-to-10 carbons possessing one or more carbon-carbon double bonds including, but not limited to, cyclopentenyl, cyclohexenyl, 1,3,3-trimethylcyclohexenyl, and the like, in which the point of attachment may occur at any available valency on the carbocylic ring.
" Cycloalkyl" refers to saturated cyclic groups of 3-to-8 carbons including, but not limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, and the like.
"Cycloalkylalkenyl" refers to cycloalkyl, as defined above, except that it is attached to the remainder of the molecule via an alkenyl group, as defined above.
" Cycloalkylalkyl" refers to a cycloalkyl group, as defined above, except that it is attached to the remainder of the molecule via an alkyl group. Examples include, but are not limited to, cyclohexylmethyl, cyclohexylethyl, and the like.
"Cycloalkylalkynyl" refers to cycloalkyl, as defined above, except that it is attached to the remainder of the molecule via an alkynyl group, as defined above.
"Guanidino" refers to a group of the structure -NR1°5C(=NR106)NHR107 or -NC(NHR1 6)NHR107, wherein R105, R106, and R107 are independently selected from hydrogen, (Ci-to-Cg-alkyl), mod-Het-, as defined below, mod-heterocy ic, as defined below, aminoalkyl, as defined above, and mod-aryl, as defined below, or alternatively, R1 6, and R107, taken together, may optionally be -(CH2)CC-, where cc is an integer of from 2-to-6.
"Halo" and "halogen" refer to an atom selected from fluorine, chlorine, bromine and iodine.
"Het-", as used herein, refers to any aromatic 5-, 6- or 7-membered monocyclic ring or a bi- or tri-cycUc group comprising fused five- or six-membered rings having ring carbon atoms and between one and three heteroatoms independently selected from oxygen, sulfur and nitrogen, wherein (i) each 5-membered ring has 2 double bonds and each 6- or 7- membered ring has 3 double bonds, (ii) the nitrogen and sulfur heteroatoms as well as the carbon atoms may optionally be oxidized, (iii) the nitrogen heteroatom may optionaUy be quaternized, (iv) any of these rings may be fused to a benzene ring, and (v) any carbon or heteroatom with suitable valence may bear a substituent, R301, as defined above. Any two adjacent R301 substituents in a di-, tri-, tetra- or penta-substituted Het group may form a 5-, 6- or 7-membered ring consisting of carbon atoms and zero, one or two heteroatoms independently selected from the group consisting of -O-, -S(O)s-, where s is as defined above, and -NR8-, where R8 is as defined above. Het groups include, but are not limited to, pyrrolyl, pyrazolyl, cytosinyl, thiocytosinyl, imidazolyl, pyridyl, pyrazinyl, pyrimidinyl, pyridazinyl, xanthenyl, xanthonyl, xanthopterinyl, oxazolyl, thiouracilyl, isoxazolyl, indolyl, quinolinyl, uracilyl, urazolyl, uricyl, thiazolyl, isothiazolyl, isoquinolinyl, thyminyl, benzimidazolyl, benzothiazolyl, benzoxazolyl, furyl, thienyl, benzothienyl, and the like.
"Heterocyclic" as used herein, except where otherwise specified, refers to any non- aromatic 5-, 6- or 7-membered monocyclic ring or a bi- or tri-cyclic group comprising fused five- or six-membered rings, having ring carbon atoms and between one-and-three heteroatoms independently selected from oxygen, sulfur and nitrogen, wherein (i) each 5- membered ring has 0 or 1 double bond and each 6-membered ring has 0 to 2 double bonds, (ii) the nitrogen and sulfur heteroatoms as well as the carbon atoms may optionally be oxidized, (iii) the nitrogen heteroatom may optionally be quaternized, (iv) any of these rings may be fused to a benzene ring, and (v) any carbon or heteroatom with suitable valence may bear a substituent, R301, as defined above. Any two adjacent R301 substituents in a di-, tri-, tetra- or penta-substituted heterocyclic group may form a 5-, 6- or 7-membered ring consisting of ring carbon atoms and zero, one or two heteroatoms independently selected from the group consisting of -O-, -S(O)s-, where s is as defined above, and -NR8-, where R8 is as defined above. Representative heterocycles include, but are not Umited to, aziridinyl, thiomorpholine, thiomorpholine-oxide, thiomorpholine dioxide, and pyrrolidinyl, pyrazolinyl, pyrazoUdinyl, imidazolinyl, imidazolidinyl, piperidinyl, piperazinyl, oxazoUdinyl, isoxazoUdinyl, morpholinyl, thiazolidinyl, and isothiazolidinyl, and the like.
"Heterocyclic alkyl" refers to a heterocyclic group, as defined above, except that it is attached to the remainder of the molecule via an alkyl group, as previously defined.
"HeterocycUc alkylether" refers to a heterocycUc alkyl moiety, as defined above, except that it is attached to the remainder of the molecule via an oxygen atom.
"Heterocyclic alkenyl" refers to a heterocyclic group, as defined above, except that it is attached to the remainder of the molecule via an alkenyl group, as previously defined.
"HeterocycUc alkylthioether" refers to a heterocyclic alkyl moiety, as defined above, except that it is attached to the remainder of the molecule via a sulfur atom.
"Heterocyclic alkynyl" refers to a heterocyclic group, as defined above, except that it is attached to the remainder of the molecule via an alkynyl group, as previously defined.
"Heterocyclic ether" refers to a heterocyclic moiety, as defined above, except that it is attached to the remainder of the molecule via an oxygen atom.
"Heterocyclic thioether" refers to a heterocyclic moiety, as defined above, except that it is attached to the remainder of the molecule via a sulfur atom. "Hydroxyalkyl" refers to an -OH appended to an alkyl group, as defined above.
"Hydroxy-protecting group" refers to those groups which are known in the art to protect a hydroxyl group against undesirable reactions during synthetic procedures and to be selectively removable including, but not Umited to, methylthiomethyl, tert- butyldimethylsilyl, tert-butyldiphenylsilyl, acyl substituted with an aryl group, where acyl and aryl are defined above, and the like.
"Leaving group" refers to an alkyl-, alkenyl-, or aryl-substituent, where alkyl, alkenyl, and aryl are as defined above, which in a reaction becomes cleaved to either produce a site of unsaturation or to introduce another substituent.
"Mod-aryl", as used herein, refers to an aryl group, as defined above, except that the aryl group is unsubstituted or substituted with from one-to-three independently selected substituents, R302, rather than R301, where R302 is as defined above. Any two adjacent R302 substituents in a di- or tri-substituted mod-aryl group may form a 5-, 6- or 7-membered carbocyclic ring or 5-, 6- or 7-membered heterocyclic-ring where the ring atoms are carbon atoms and one or two heteroatoms independently selected from the group consisting of -O-, -S(O)s-, where s is as defined above, and -NR18-, where R18 is as defined above.
"Mod-Ci-to-Cio-alkyl", as used herein, refers to a -(Ci-to-Cio-alkyl) group substituted with from one-to-six radicals selected from:
(1) -R8 , as defined above;
(2) -(CH2)mOR8, where m and R8 are as defined above;
(3) -S(O)sR8, where s and R8 are as defined above;
(4) -S(O)tNR8R9, where t and NR R9 are as defined above;
(5) -(CH2)mNR8R9, where m and NR R9 are as defined above;
(6) -SO3H;
(7) =NOR8, where R8 is as defined above;
(8) -R399, as defined above;
(9) -R400, as defined above;
(10) -aryl; and
(11) -Het.
"Mod-C3-to-Cιo-alkenyl", as used herein, refers to a -(C3-to-Cιo-alkenyl) group substituted with from one-to-six radicals selected from:
(1) -R8, where R8 is as defined above;
(2) -(CH2)mOR8, where m and R8 are as defined above;
(3) -S(O)sR8, where s and R8 are as defined above;
(4) -S(O)tNR8R9, Where t and NR8R9 are as defined above;
(5) -(CH2)mNR8R9, where m and NR8R9 are as defined above;
(6) -SO3H;
(7) =NOR8, where R8 is as defined above; (8) -R399, where R399 is as defined above;
(9) -R400, where R400 is as defined above;
(10) -aryl; and
(11) -Het.
"Mod-C3-to-Cιo-alkynyl", as used herein, refers to a -(C3-to-Cιo-alkynyl) group substituted with from one-to-six radicals selected from:
(1) -R8, where R8 is as defined above;
(2) -(CH )mOR8, where m and R8 are as defined above;
(3) -S(O)sR8, where s and R8 are as defined above;
(4) -S(O)tNR8R9, where t and NR8R9 are as defined above;
(5) -(CH2)mNR8R9, where m and NR8R9 are as defined above;
(6) -SO3H;
(7) =NOR8, where R8 is as defined above;
(8) -R399, where R399 is as defined above;
(9) -R400, where R400 is as defined above;
(10) -aryl; and
(11) -Het.
"Mod-cyclo-C3-to-Cιo-alkyl", as used herein, refers to a -(cyclo-C3-to-Cιo-alkyl) group substituted with from one-to-six radicals selected from:
(1) -R8, where R8 is as defined above;
(2) -(CH2)mOR8, where m and R8 are as defined above;
(3) -S(O)sR8, where s and R8 are as defined above;
(4) -S(O)tNR8R9, where t and NR8R9 are as defined above;
(5) -(CH )mNR8R9, where m and NR8R9 are as defined above;
(6) -SO3H;
(7) =NOR8, where R8 is as defined above;
(8) -R399, where R 99 is as defined above;
(9) -R400, where R400 is as defined above;
(10) -aryl; and
(11) -Het.
"Mod-cyclo-C4-to-Cιo-alkenyl", as used herein, refers to a -(cyclo-C4-to-Cιo- alkenyl) group substituted with from one-to-six radicals selected from:
(1) -R8, where R8 is as defined above;
(2) -(CH2)mOR8, where m and R8 are as defined above;
(3) -S(O)sR8, where s and R8 are as defined above;
(4) -S(O)tNR8R9, where t and NR8R9 are as defined above;
(5) -(CH2)mNR8R9, where m and NR8R9 are as defined above;
(6) -SO3H; (7) =NOR8, where R8 is as defined above;
(8) -R399, where R399 is as defined above;
(9) -R400, where R400 is as defined above;
(10) -aryl; and
(11) -Het.
"Mod-bicyclo-C6-to-Cιo-alkyl", as used herein, refers to a -(bicyclo-C6-to-Cιo-alkyl) group substituted with from one-to-six radicals selected from:
(1) -R8, where R8 is as defined above;
(2) -(CH2)mOR8, where m and R8 are as defined above;
(3) -S(O)sR8, where s and R8 are as defined above;
(4) -S(O)tNR8R9, where t and NR8R9 are as defined above;
(5) -(CH2)mNR8R9, where m and NR8R9 are as defined above;
(6) -SO3H;
(7) =NOR8, where R8 is as defined above;
(8) -R399, where R399 is as defined above;
(9) -R400, where R400 is as defined above;
(10) -aryl; and
(11) -Het.
"Mod-bicyclo-C6-to-Cιo-alkenyl", as used herein, refers to a -(bicyclo-C6-to-Cιo- alkenyl) group substituted with from one-to-six radicals selected from:
(1) -R8, as defined above;
(2) -(CH2)mOR8, where m and R8 are as defined above;
(3) -S(O)sR8, where s and R8 are as defined above;
(4) -S(O)tNR8R9, where t and NR8R9 are as defined above;
(5) -(CH2)mNR8R9, where m and NR8R9 are as defined above;
(6) -SO3H;
(7) =NOR8, where R8 is as defined above;
(8) -R399, is as defined above;
(9) -R400, is as defined above;
(10) -aryl; and
(11) -Het.
"Mod-Het-", as used herein, refers to a Het group, as defined above, except that the Het group may bear one or more substituents R302, rather than R301, where R302 is as defined above or any two adjacent R302 substituents in a di-, tri-, tetra- or penta-substituted mod-Het group may form a 5-, 6- or 7-membered ring consisting of ring carbon atoms and zero, one or two ring heteroatoms independently selected from the group consisting of -O-, -S(O)s-, where s is as defined above, and -NR18-, where R18 is as defined above. "Mod-heterocyclic" as used herein, refers to a heterocycUc group, as defined above, except that the heterocycUc group may bear one or more substituents R302, rather than R301, where R302 is as defined above or any two adjacent R302 substituents in a di-, tri-, tetra- or penta-substituted mod-heterocylic group may form a 5-, 6- or 7-membered ring consisting of carbon atoms and zero, one or two heteroatoms independently selected from the group consisting of -O-, -S(O)s-, where s is as defined above, and -NR18-, where R18 is as defined above.
"Monoalkylamino" and "dialkylamino" refer respectively to one and two alkyl groups, as defined above, except that they are appended to the remainder of the molecule via an amino group. Examples include, but are not Umited to, methylamino, isopropylamino, dimethylamino, N,N-methylisopropylamino, and the like.
"Monocycloalkylamino" and "dicycloalkylamino" refer respectively to one and two cycloalkyl groups, as defined above, except that they are appended to the remainder of the molecule via an amino group. Examples include, but are not limited to, cyclohexylamino, b._.-(cyclohexyl)amino, and the like.
"Mono-halogenated alkyl", "di-halogenated alkyl" or "tri-halogenated alkyl" refer to alkyl groups, as defined above, of specified and compatible length, respectively substituted with one, two, or three halogen atoms, as defined above.
"N-alkylcarboxamido" refers to an alkylamino group, as defined above, except that it is appended to the remainder of the molecule via a carbonyl group and has the formula HN(alkyl)C(O)-.
"N-arylcarboxamido" refers to an arylamino group, as defined above, except that it is appended to the remainder of the molecule via a carbonyl group and having the formula HN(aryl)C(O)-.
"Naturally occuring amino acid" and "standard amino acid" refer to an amino acid selected from the group consisting of alanine, arginine, asparagine, aspartic acid, cysteine, glutamine, glutamic acid, glycine, histidine, isoleucine, leucine, lysine, methionine, phenylalanine, proUne, serine, threonine, tryptophan, tyrosine and valine.
"N,N-dialkylcarboxamido" refers to dialkylamino group, defined above, except that it is appended to the remainder of the molecule via a carbonyl group and has the formula N(alkyl)(alkyl')C(O)-.
"N,N-diarylcarboxamido" refers to two independently selected aryl groups, as defined above, except that they are appended to the remainder of the molecule via a =NC(O)- group, exempUfied by the formula N(aryl)(aryl)C(O)-.
"N-terminal protecting group" refers to those groups known in the art to protect the N-terminus against undesirable reactions during synthetic procedures or to prevent the attack of exopeptidases on the final compounds or to increase the solubility of the final compounds and includes, but is not limited to acyl, acetyl, pivaloyl, tert-butylacetyl, tert- butyloxycarbonyl (Boc), benzyloxycarbonyl (Cbz), benzoyl groups, and the like. Other such groups are described by Gross, E. and Meienhofer, J. in The Peptides. Volume 3; Academic Press, 1981."
"Oxo" refers to an oxygen atom forming a carbonyl group.
"Per-halogenated alkyl" refers to alkyl groups, as defined above, of specified length, substituted with halogen atoms, as defined above, at every available valency.
"Qualified-aryl" as used herein refers to substituted and unsubstituted carbocycUc aromatic groups including, but not Umited to, phenyl, 1- or 2-naphthyl, fluorenyl, (1,2)- dihydronaphthyl, (l,2,3.4)-tetrahydronaphthyl, indenyl, indanyl and the like, optionally substituted with 1, 2 or 3 substituents independently selected from halo, nitro, cyano, -(Cj-to-Cio-alkyl), alkoxy and halosubstituted alkyl.
"Qualified-arylalkyl" refers to a qualified-aryl group, as previously defined, attached to the remainder of the molecule via an alkyl group.
"Sub-Cι-to-Cιo-alkyl", as used herein, refers to a -(Cι-to-Cιo-alkyl) substituted with from one-to-six radicals independently selected from the group consisting of:
(a) R6, where R6 is as defined above;
(b) -(CH2)mOR6, where m and R6 are as defined above;
(c) -NR6R7, where NR6R7 is as defined above;
(d) -C(O)OR6, where R6 is as defined above;
(e) -SO3H;
(f) -S(O)sR6, where s and R6 are as defined above;
(g) -S(O)tNR6R7, where t and NR6R7 are as defined above; (h) =NOR6, where R6 is as defined above;
(i) -R 99, where R399 is as defined above;
(j) -R400, where R400 is as defined above;
(k) -aryl, and
(1) -Het. "Sub-cyclo-C3-to-Cιo-alkyl", as used herein, refers to a -(cyclo-C3-to-Cιo-alkyl) substituted with from one-to-six radicals independently selected from the group consisting of:
(a) R6, where R6 is as defined above;
(b) -(CH2)mOR6, where m and R6 are as defined above;
(c) -NR6R7, where NR6R7 is as defined above;
(d) -C(O)OR6, where R6 is as defined above;
(e) -SO3H;
(f) -S(O)sR6, where s and R6 are as defined above;
(g) -S(O)tNR6R7, where t and NR6R7 are as defined above; (h) =NOR6, where R6 is as defined above; (i) -R399, where R399 is as defined above;
(j) -R400, where R400 is as defined above;
(k) -aryl, and
(1) -Het. "Sub-cyclo-C3-to-Cιo-alkyl-Cι-to-C3-alkyl", as used herein, refers to a -(cyclo- C3-to-Cιo-alkyl-Cι-to-C3-alkyl) substituted with from one-to-six radicals independently selected from the group consisting of:
(a) R6, where R6 is as defined above;
(b) -(CH2)mOR6, where m and R6 are as defined above;
(c) -NR6R7, where NR6R7 are as defined above;
(d) -C(O)OR6, where R6 is as defined above;
(e) -SO3H;
(f) -S(O)sR6, where s and R6 are as defined above;
(g) -S(O)tNR6R7, where t and NR6R7 are as defined above; (h) =NOR6, where R6 is as defined above;
(i) -R399, where R399 is as defined above; (j) -R400, where R400 is as defined above; (k) -aryl, and (1) -Het. "Sub-C3-to-Cιo-alkenyl", as used herein, refers to a -(C3-to-Cιo-alkenyl) substituted with from one-to-six radicals independently selected from the group consisting of:
(a) R6, where R6 is as defined above;
(b) -(CH2)mOR6, where m and R6 are as defined above;
(c) -NR6R7, where NR6R7 are as defined above;
(d) -C(O)OR6, where R6 is as defined above;
(e) -SO3H;
(f) -S(O)sR6, where s and R6 are as defined above;
(g) -S(O)tNR6R7, where t and NR6R7 are as defined above; (h) =NOR6, where R6 is as defined above;
(i) -R399, where R399 is as defined above;
(j) -R400, where R400 is as defined above;
(k) -aryl, and
(1) -Het. "Sub-cyclo-C4-to-Cιo-alkenyl", as used herein, refers to a -(cyclo- -to-Cio-alkenyl) substituted with from one-to-six radicals independently selected from the group consisting of:
(a) R6, where R6 is as defined above;
(b) -(CH2)mOR6, where m and R6 are as defined above; (c) -NR6R7, where NR6R7 are as defined above;
(d) -C(O)OR6, where R6 is as defined above;
(e) -SO3H;
(f) -S(O)sR6, where s and R6 are as defined above;
(g) -S(O)tNR6R7, where t and NR6R7 are as defined above; (h) =NOR6, where R6 is as defined above;
(i) -R399, where R399 is as defined above;
(j) -R400, where R400 is as defined above;
(k) -aryl, and
(1) -Het. "Sub-cyclo-C6-to-Cιo-alkyl-C3-C5-alkenyl", as used herein, refers to a -(cyclo- C6-to-Cιo-alkyl-C3-C5-alkenyl) substituted with from one-to-six radicals independently selected from the group consisting of:
(a) R6, where R6 is as defined above;
(b) -(CH2)mOR6, where m and R6 are as defined above;
(c) -NR6R7, where NR6R7 are as defined above;
(d) -C(O)OR6, where R6 is as defined above;
(e) -SO3H;
(f) -S(O)sR6, where s and R6 are as defined above;
(g) -S(O)tNR6R7, where t and NR6R7 are as defined above; (h) =NOR6, where R6 is as defined above;
(i) -R399, where R399 is as defined above; (j) -R400, where R400 is as defined above; (k) -aryl, and (1) -Het. "Sub-C3-to-Cιo-alkynyl", as used herein, refers to a -(C3-to-Cιo-alkynyl) substituted with from one-to-six radicals independently selected from the group consisting of:
(a) R6, as defined above;
(b) -(CH2)mOR6, where m and R6 are as defined above;
(c) -NR6R7, as defined above;
(d) -C(O)OR6, where R6 is as defined above;
(e) -SO3H;
(f) -S(O)sR6, where s and R6 are as defined above;
(g) -S(O)tNR6R7, where t and NR6R7 are as defined above; (h) =NOR6, where R6 is as defined above;
(i) -R399, as defined above; (j) -R400, as defined above; (k) -aryl, and (1) -Het. "Sub-cyclo-C6-to-Cιo-alkyl-C3-C5-alkynyl", as used herein, refers to a -(cyclo- C6τto-Cιo-alkyl-C3-C5-alkynyl) substituted with from one-to-six radicals independently selected from the group consisting of:
(a) R6, as defined above;
(b) -(CH2)mOR6, where m and R6 are as defined above;
(c) -NR6R7, as defined above;
(d) -C(O)OR6, where R6 is as defined above;
(e) -SO3H;
(f) -S(O)sR6, where s and R6 are as defined above;
(g) -S(O)tNR6R7, where t and NR6R7 are as defined above; (h) =NOR6, where R6 is as defined above;
(i) -R399, is as defined above;
(j) -R400, is as defined above;
(k) -aryl, and
(1) -Het. "Sub-bicyclo-C6-to-Cιo-alkyl", as used herein, refers to a -(bicyclo-Cg-to-Cio-alkyl) substituted with from one-to-six radicals independently selected from the group consisting of:
(a) R6, as defined above;
(b) -(CH2)mOR6, where m and R6 are as defined above;
(c) -NR6R7, as defined above;
(d) -C(O)OR6, where R6 is as defined above;
(e) -SO3H;
(f) -S(O)sR6, where s and R6 are as defined above;
(g) -S(O)tNR6R7, where t and NR6R7 are as defined above; (h) =NOR6, where R6 is as defined above;
(i) -R399, where R3" is as defined above;
(j) -R400, where R400 is as defined above;
(k) -aryl, and
(1) -Het. "Sub-bicyclo-Cg-to-Cio-alkenyl", as used herein, refers to a -(bicyclo-Cg-to- o- alkenyl) substituted with from one-to-six radicals independently selected from the group consisting of:
(a) R6, as defined above;
(b) -(CH2)mOR6, where m and R6 are as defined above;
(c) -NR6R7, as defined above;
(d) -C(O)OR6, where R6 is as defined above; (e) -SO3H;
(f) -S(O)sR6, where s and R6 are as defined above;
(g) -S(O)tNR6R7, where t and NR6R7 are as defined above; (h) =NOR6, where R6 is as defined above;
(i) -R399, is as defined above; (j) -R400, is as defined above; (k) -aryl, and (1) -Het. "Substituted-bicyclo-C6-to-Cιo-alkenyl", as used herein, refers to a -(bicyclo-
C6-to-Cιo-alkenyl) group substituted with from one-to-three radicals selected from: halogen; -OH; (Cι-C6-alkyl)NH-; di(Cι-C6-alkyl)N-; -CO2H; -CONH2; -SH; (Cι-C6-alkyl)S-; (Cι-C6-alkyl)O-; (Cι-C6-alkyl)OC(O)-;mod-aryl-(Cι-C6- alkyl)OC(O)-; (Cι-C6-alkyl)OC(O)NH-; (C -C6-alkyl)C(O)NH-; mod-aryl- (Cι-C6-alkyl)OC(O)NH-; mod-aryl-OC(O)NH-; (Cι-C6-alkyl)CO-guanidino; mod-aryl-(SO2)-guanidino; (Cι-C6-alkyl)OC(O)-guanidino; H2N-; mod-aryl- (Cι-C6-alkyl)OC(O)-guanidino; mod-aryl-OC(O)-guanidino; (Ci- - alkyl)NHC(O)-; di(Cι-C6-alkyl)NC(O)-; mod-aryl-NHCO-; di(mod- aryl)NCO-; -OSO2R11; oxo; epoxy; mod-aryl-O-; mod-aryl-S-; mod-aryl-(Cι- C6-alkyl)O-; mod-aryl-(Cι-C6-alkyl)-S-; mod-Het-O-; mod-Het-S-; mod-Het- (Cι-C6-alkyl)O; mod-Het-(Cι-C6-alkyl)S-; mod-aryl; mod-Het-; -SO3H; -S(O)tNH2; -S^tNHR11; -S O^NR^R11 , where both R^'s are independently selected; and -S(O)sR11; wherein guanidino, mod-aryl, oxo, epoxy, mod-Het-, s, t and R11 are as defined above. "Substituted-bicyclo-C6-to-Cιo-alkyl", as used herein, refers to a -(bicyclo-C6-to-Cιo- alkyl) group substituted with from one-to- three radicals selected from: halogen; -OH; (Cι-C6-alkyl)NH-; di(Cι-C6-alkyl)N-; -CO2H; -CONH2; -SH; (Cι-C6-alkyl)S-; (Cι-C6-alkyl)O-; (Cι-C6-alkyl)OC(O)-;mod-aryl-(Cι-C6- alkyl)OC(O)-; (Cι-C6-alkyl)OC(O)NH-; (Cι-C6-alkyl)C(O)NH-; mod-aryl- (Cι-C6-a_kyl)OC(O)NH-; mod-aryl-OC(O)NH-; (Cι-C6-alkyl)CO-guanidino; mod-aryl-(SO2)-guanidino; (Cι-C6-alkyl)OC(O)-guanidino; H2N-; mod-aryl- (Cι-C6-alkyl)OC(O)-guanidino; mod-aryl-OC(O)-guanidino; (Ci- - alkyl)NHC(O)-; di(Cι-C6-alkyl)^C(O)-; mod-aryl-NHCO-; di(mod- aryl)NCO-; -OSO2R11; oxo; epoxy; mod-aryl-O-; mod-aryl-S-; mod-aryl-(Cι- C6-alkyl)O-; mod-aryl-(Cι-C6-alkyl)-S-; mod-Het-O-; mod-Het-S-; mod-Het- (Cι-C6-alkyl)O; mod-Het-(Cι-C6-alkyl)S-; mod-aryl; mod-Het-; -SO H; -S(O)tNH2; -S(O)tNHR11; -S^tNR^R 1 , where both R^'s are independently selected; and -S(O)sR11; wherein guanidino, mod-aryl, oxo, epoxy, mod-Het-, s, t and R11 are as defined above. "Substituted-C3-to-C6-alkenyl", as used herein, refers to a -(C3-to-C6-alkenyl) group substituted with from one-to-three radicals selected from: halogen; -OH; (Cι-C6-alkyl)NH-; di(Cι-C6-alkyl)N-; -CO2H; -CONH2; -SH; (Cι-C6-alkyl)S-; (Cι-C6-alkyl)O-; (Cι-C6-alkyl)OC(O)-;mod-aryl-(Cι-C6- alkyl)OC(O)-; (Cι-C6-alkyl)OC(O)NH-; (Cι-C6-alkyl)C(O)NH-; mod-aryl- (Cι-C6-alkyl)OC(O)NH-; mod-aryl-OC(O)NH-; (Cι-C6-alkyl)CO-guanidino; mod-aryl-(SO2)-guanidino; (Cι-C6-alkyl)OC(O)-guanidino; H2N-; mod-aryl- (Cι-C6-alkyl)OC(O)-guanidino; mod-aryl-OC(O)-guanidino; (Ci- - alkyl)NHC(O)-; di(Cι-C6-alkyl)NC(O)-; mod-aryl-NHCO-; di(mod- aryl)NCO-; -OSQ2R11; oxo; epoxy; mod-aryl-O-; mod-aryl-S-; mod-aryl-(Cι- C6-alkyl)O-; mod-aryl-(Cι-C6-alkyl)-S-; mod-Het-O-; mod-Het-S-; mod-Het- (Cι-C6-alkyl)O; mod-Het-(Cι-C6-alkyl)S-; mod-aryl; mod-Het-; -SO3H; -S(O)tNH ; -S^NHR11; -S(O)tNR11R11 , where both Rn's are independently selected; and -S(O)sR11; wherein guanidino, mod-aryl, oxo, epoxy, mod-Het-, s, t and R11 are as defined above. "Substituted-Cι-to-C6-alkyl", as used herein, refers to a -(Ci-to- -alkyl) group substituted with from one-to-three radicals selected from: halogen; -OH; (Cι-C6-alkyl)NH-; di(Cι-C6-alkyl)N-; -CO2H; -CONH2; -SH; (Cι-C6-alkyl)S-; (Cι-C6-alkyl)O-; (Cι-C6-alkyl)OC(O)-;mod-aryl-(Cι-C6- alkyl)OC(O)-; (Cι-C6-alkyl)OC(O)NH-; (Cι-C6-alkyl)C(O)NH-; mod-aryl- (Cι-C6-alkyl)OC(O)NH-; mod-aryl-OC(O)NH-; (Cι-C6-alkyl)CO-guanidino; mod-aryl-(SO )-guanidino; (Cι-C6-alkyl)OC(O)-guanidino; H2N-; mod-aryl- (Cι-C6-alkyl)OC(O)-guanidino; mod-aryl-OC(O)-guanidino; (Ci- - alkyl)NHC(O)-; di(Cι-C6-alkyl)NC(O)-; mod-aryl-NHCO-; di(mod- aryl)NCO-; -OSO2R11; oxo; epoxy; mod-aryl-O-; mod-aryl-S-; mod-aryl-(Cι- C6-alkyl)O-; mod-aryl-(Cι-C6-alkyl)-S-; mod-Het-O-; mod-Het-S-; mod-Het- (Cι-C6-alkyl)O; mod-Het-(Cι-C6-alkyl)S-; mod-aryl; mod-Het-; -SO3H; -S(O)tNH2; -S^tNHR11; -S O^NR^R11 , where both RU's are independently selected; and -S(O)sR11; wherein guanidino, mod-aryl, oxo, epoxy, mod-Het-, s, t and R11 are as defined above. "Substituted-C3-to-C6-alkynyl", as used herein, refers to a -(C3-to-C6-alkynyl) group substituted with from one-to-three radicals selected from: halogen; -OH; (Cι- -alkyl)NH-; di(Cι-C6-alkyl)N-; -CO2H; -CONH2; -SH; (Cι-C6-alkyl)S-; (Cι-C6-alkyl)O-; (Cι-C6-alkyl)OC(O)-;mod-aryl-(Cι-C6- alkyl)OC(O)-; (Cι-C6-alkyl)OC(O)NH-; (Cι-C6-alkyl)C(O)NH-; mod-aryl- (Cι-C6-alkyl)OC(O)NH-; mod-aryl-OC(O)NH-; (Cι-C6-alkyl)CO-guanidino; mod-aryl-(SO )-guanidino; (Cι-C6-alkyl)OC(O)-guanidino; H2N-; mod-aryl- (Cι-C6-alkyl)OC(O)-guanidino; mod-aryl-OC(O)-guanidino; (Ci-Cβ- alkyl)NHC(O)-; di(Cι-C6-alkyl)NC(O)-; mod-aryl-NHCO-; di(mod- aryl)NCO-; -OSO R11; oxo; epoxy; mod-aryl-O-; mod-aryl-S-; mod-aryl-(Cι- C6-alkyl)O-; mod-aryl-(Cι-C6-alkyl)-S-; mod-Het-O-; mod-Het-S-; mod-Het- (Cι-C6-alkyl)O; mod-Het-(Cι- -__lkyl)S-; mod-aryl; mod-Het-; -SO3H; -S(O)tNH ; -S(0)tNHR11; -S^NR1^11 , where both R 's are independently selected; and -S(O)sR11; wherein guanidino, mod-aryl, oxo, epoxy, mod-Het-, s, t and R11 are as defined above. "Substituted-cyclo-C4-to-Cιo-alkenyl", as used herein, refers to a -(cyclo-C4-to-Cιo- alkenyl) group substituted with from one-to-three radicals selected from: halogen; -OH; (Cι-C6-alkyl)NH-; di(Cι-C6-alkyl)N-; -CO2H; -CONH2; -SH; (Cι-C6-alkyl)S-; (Cι-C6-alkyl)O-; (Cι-C6-alkyl)OC(O)-;mod-aryl-(Cι-C6- alkyl)OC(O)-; (Cι-C6-alkyl)OC(O)NH-; (Cι-C6-alkyl)C(O)NH-; mod-aryl- (Cι-C6-alkyl)OC(O)NH-; mod-aryl-OC(O)NH-; (Cι-C6-alkyl)CO-guanidino; mod-aryl-(SO2)-guanidino; (Cι-Cg-alkyl)OC(O)-guanidino; H2N-; mod-aryl- (Cι-C6-alkyl)OC(O)-guanidino; mod-aryl-OC(O)-guanidino; (C1-Q5- alkyl)NHC(O)-; di(Cι-C6-alkyl)NC(O)-; mod-aryl-NHCO-; di(mod- aryl)NCO-; -OSO R11; oxo; epoxy; mod-aryl-O-; mod-aryl-S-; mod-aryl-(Cι- C6-alkyl)O-; mod-aryl-(Cι-C6-alkyl)-S-; mod-Het-O-; mod-Het-S-; mod-Het- (Cι-C6-alkyl)O; mod-Het-(Cι-C6-alkyl)S-; mod-aryl; mod-Het-; -SO3H; -S(O)tNH2; , where both RH's are independently selected; and -S(O)sR11; wherein guanidino, mod-aryl, oxo, epoxy, mod-Het-, s, t and R11 are as defined above. "Substituted-cyclo-C3-to-Cιo-alkyl", as used herein, refers to a -(cyclo-C3-to-Cιo- alkyl) group substituted with from one-to-three radicals selected from: halogen; -OH; (Cι-C6-alkyl)NH-; di(Cι-C6-alkyl)N-; -CO2H; -CONH2; -SH;
(Cι-C6-alkyl)S-; (Cι-C6-alkyl)O-; (Cι-C6-alkyl)OC(O)-;mod-aryl-(Cι-C6- alkyl)OC(O)-; (Cι-C6-alkyl)OC(O)NH-; (Cι-C6-alkyl)C(O)NH-; mod-aryl- (Cι-C6-alkyl)OC(O)NH-; mod-aryl-OC(O)NH-; (Cι-C6-alkyl)CO-guanidino; mod-aryl-(SO2)-guanidino; (Cι-C6-alkyl)OC(O)-guanidino; H2N-; mod-aryl- (Cι-C6-alkyl)OC(O)-guanidino; mod-aryl-OC(O)-guanidino; (Ci- - alkyl)NHC(O)-; di(Cι-C6-alkyl)NC(O)-; mod-aryl-NHCO-; di(mod- aryl)NCO-; -OSO2R11; oxo; epoxy; mod-aryl-O-; mod-aryl-S-; mod-aryl-(Cι- C6-alkyl)O-; mod-aryl-(Cι-C6-alkyl)-S-; mod-Het-O-; mod-Het-S-; mod-Het- (Cι-C6-alkyl)O; mod-Het-(Cι-C6-alkyl)S-; mod-aryl; mod-Het-; -SO3H; -S(O)tNH2; -S OtNHR11; -S(O)tNR11R11 , where both RU's are independently selected; and -S(O)sR11; wherein guanidino, mod-aryl, oxo, epoxy, mod-Het-, s, t and R11 are as defined above. "Substituted-bicyclo-C6-to-Cιo-alkenyl-Cι-to-C6-alkyl", as used herein, refers to a -(bicyclo-C6-to-Cιo-alkenyl)-Cι-to-C6-alkyl group substituted with from one-to-three radicals selected from: halogen; -OH; (Cι-C6-alkyl)NH-; di(Cι-C6-alkyl)N-; -CO2H; -CONH2; -SH; (Cι-C6-alkyl)S-; (Cι-C6-alkyl)O-; (Cι-C6-alkyl)OC(O)-;mod-aryl-(Cι-C6- alkyl)OC(O)-; (Cι-C6-alkyl)OC(O)NH-; (Cι-C6-alkyl)C(O)NH-; mod-aryl- (Cι-C6-alkyl)OC(O)NH-; mod-aryl-OC(O)NH-; (Cι-C6-alkyl)CO-guanidino; mod-aryl-(SO2)-guanidino; (Cι-C6-alkyl)OC(O)-guanidino; H2N-; mod-aryl- (Cι-C6-alkyl)OC(O)-guanidino; mod-aryl-OC(O)-guanidino; (Ci- - alkyl)NHC(O)-; di(Cι-C6-alkyl)NC(O)-; mod-aryl-NHCO-; di(mod- aryl)NCO-; -OSC^R11; oxo; epoxy; mod-aryl-O-; mod-aryl-S-; mod-aryl-(Cι- C6-alkyl)O-; mod-aryl-(Cι-C6-alkyl)-S-; mod-Het-O-; mod-Het-S-; mod-Het- (Cι-C6-aUcyl)O; mod-Het-(Cι-C6-alkyl)S-; mod-aryl; mod-Het-; -SO3H; -S(O)tNH2; -S(O)tNHR11; -S O^NR^R11 , where both R^'s are independently selected; and -S(O)sR11; wherein guanidino, mod-aryl, oxo, epoxy, mod-Het-, s, t and R11 are as defined above. "Thioalkoxyalkyl" refers to a thioalkoxy group, as defined above, except that it is attached to the remainder of the molecule via an alkyl group.
"Thiolalkyl" refers to an alkyl group, as defined above, substituted with an -SH group. "Thiooxo" refers to a sulfur atom forming a thiocarbonyl group. "Unsubstituted aryl" refers to mono-, di-, tri- or tetracyclic aromatic groups, charged or uncharged, the rings of which are comprised of from 3-to-7 carbon atoms. Examples of unsubstituted aryl include, but are not Umited to, phenyl, 1- or 2-naphthyl, azulenyl, fluorenyl, (1, 2)-dihydronaphthyl, (l,2,3.4)-tetrahydronaphthyl, indenyl, indanyl and the like, which are solely substituted by hydrogen.
"Pharmaceutically-acceptable salts, esters, amides and prodrugs" refers to those carboxylate salts, amino acid addition salts, esters, amides and prodrugs of the compounds of the present invention which are, within the scope of sound medical judgement, suitable for use in contact with the tissues of humans and lower animals without undue toxicity, irritation, allergic response, or the like, commensurate with a reasonable benefit/risk ratio, and effective for their intended use, as well as the zwitterionic forms, where possible, of the compounds of the invention. The term "salts" refers to the relatively non-toxic, inorganic and organic acid addition salts of compounds of the present invention, which may be prepared in situ during the final isolation and purification of the compounds or by separately reacting the purified compound in its free base form with a suitable organic or inorganic acid and isolating the salt thus formed. Representative salts include the hydrobromide, hydrochloride, sulfate, bisulfate, phosphate, nitrate, acetate, oxalate, valerate, oleate, palmitate, stearate, laurate, borate, benzoate, lactate, phosphate, tosylate, citrate, maleate, fumarate, succinate, tartrate, naphthylate, mesylate, glucoheptonate, lactiobionate and laurylsulphonate salts and the like. These may include cations based on the alkali and alkaline earth metals, such as sodium, lithium, potassium, calcium, magnesium and the like, as well as nontoxic ammonium, quaternary ammonium and amine cations including, but not limited to, ammonium, tetramethylammonium, tetraethylammonium, methylamine, dimethylamine, trimethylamine, triethylamine, ethylamine, and the like (see, for example S. M. Berge, et al., "Pharmaceutical Salts." J. Pharm. Sci. 66: 1-19 (1977)).
Examples of pharmaceutically-acceptable, non-toxic esters of the compounds of this invention include Cι-to-C6-alkyl esters wherein the alkyl group is a straight or branched chain. Acceptable esters also include Cs-to-Cγ-cycloalkyl esters as well as arylalkyl esters such as, but not Umited to benzyl. Cι-to-C4 alkyl esters are prefeπed. Esters of the compounds of the present invention may be prepared according to conventional methods. Conversely, non-toxic esters of alcoholic moieties on the compounds of the invention may be constructed by condensing these alcohols with Cι-to-C6-alkyl carboxylic acids, Cι-to-C6- alkyl dicarboxylic acids or aryl-carboxylic acids. Examples of such esters include, but are not limited to acetyl, benzoyl or hemi-succinyl.
Examples of pharmaceutically-acceptable, non-toxic amides of the compounds of this invention include amides derived from ammonia, primary Cι-to-C6- alkyl amines and secondary di-Cι-to-C6-alkyl amines. In the case of secondary amines the amine may also be in the form of a 5-or- 6 membered heterocycle containing one nitrogen atom. Amides derived from ammonia, Cι-to-C3-alkyl primary amides and di-Cι-to-C2-alkyl secondary amides are prefeπed. Amides of the compounds of the invention may be prepared according to conventional methods.
"Prodrug" refers to compounds that are rapidly transformed in vivo to yield the parent compound of the above formula, for example, by hydrolysis in blood. A thorough discussion is provided in T. Higuchi and V. Stella, "Pro-drugs as Novel DeUvery Systems", Vol 14 of the A.C.S. Symposium Series, and in Bioreversible Carriers in Drug Design, ed. Edward B. Roche, American Pharmaceutical Association and Pergamon Press, 1987.
Prodrugs of compounds of the present invention may be prepared by suitable methods. For those compounds in which the prodrug moiety is an amino acid or peptide functionality, the condensation of the drug's amino group with amino acids and peptides may be effected in accordance with conventional condensation methods such as the azide method, the mixed acid anhydride method, the DCC (dicyclohexylcarbodiimide) method, the active ester method (p-nitrophenyl ester method, N-hydroxysuccinic acid imide ester method, cyanomethyl ester method and the like), the Woodward reagent K method, the DCC-HOBT (1 -hydroxy- benzotriazole) method and the like. Classical methods for amino acid condensation reactions are described in "Peptide Synthesis" Second Edition, M. Bodansky, Y.S. Klausner and M.A. Ondetti (1976).
As in conventional peptide synthesis, branched chain amino and carboxyl groups at alpha and omega positions in amino acids may be protected and deprotected if necessary. The protecting groups for amino groups which can be used involve, for example, benzyloxycarbonyl (Z or Cbz), o-chlorobenzyloxycarbonyl ((2-Cl)Z)), p- nitrobenzyloxycarbonyl (Z(NO2)), p-methoxybenzyloxycarbonyl (Z(OMe)), t- amyloxycarbonyl (Aoc), isobornealoxycarbonyl, adamantyloxycarbonyl (Adoc), 2-(4- biphenyl)-2-propyloxy carbonyl (Bpoc), 9-fluorenyl-methoxycarbonyl (Fmoc), methylsulfonylethoxy carbonyl (Msc), trifluoroacetyl, phthalyl, formyl, 2- nitrophenylsulfonyl (Nps), diphenylphosphinothioyl (Ppt), dimethylphosphino-thioyl (Mpt), and the like.
The examples for protecting groups for carboxyl groups involve, for example, benzyl ester (OBzl), cyclohexyl ester, 4-nitrobenzyl ester (OBzlNO2), t-butyl ester (OtBu), 4- pyridylmethyl ester (OPic), and the like.
In the course of the synthesis of certain of the compounds of the present invention, specific amino acids having functional groups other than amino and carboxyl groups in the branched chain such as arginine, cysteine, serine and the like may be protected, if necessary, with suitable protecting groups. It is preferable that, for example, the guanidino group (NG) in arginine may be protected with nitro, p-toluenesulfonyl (Tos), benzyloxycarbonyl (Z), adamantyloxycarbonyl (Adoc), p-methoxybenzenesulfonyl, 4-methoxy-2,6-dimethyl- benzenesulfonyl (Mts) and the like; the thiol group in cysteine may be protected with benzyl, p-methoxybenzyl, triphenylmethyl, acetamidomethyl, ethylcarbamyl, 4-methylbenzyl (4-MeBzl), 2,4,6-trimethylbenzyl (Tmb) and the like; and the hydroxy group in serine may be protected with benzyl (Bzl), t-butyl, acetyl, tetrahydropyranyl (THP), and the like.
Numerous asymmetric centers exist in the compounds of the present invention. Except where otherwise noted, the present invention contemplates the various stereoisomers and mixtures thereof.
The potent immunomodulatory activity which compounds of the instant invention demonstrate, in common in vitro biological assays, indicate that these compounds possess immunosuppressive, antimicrobial, antifungal, antiviral, antunflammatory, and antiproliferative activity, and possess the abiUty to reverse chemotherapeutic drug resistance. As agents which block T-cell activation, a prerequisite for HIV proliferation, the compounds are useful as prophylactics for the prevention of HIV replication. While the compounds of the invention would be useful when used alone, combination therapy with other immunosuppressants, such as, FK506, rapamycin, cyclosporin A, picibanil, mycophenolic acid, azathioprine, prednisolone, cyclophosphamide, brequinar and leflunomide, would also be expected to be beneficial.
As immunosuppressants, the compounds of the present invention are useful when administered for the prevention immune-mediated tissue or organ graft rejection. Examples of transplanted tissues and organs which suffer from these effects are heart, kidney, liver, . medulla ossium, skin, cornea, lung, pancreas, intestinum tenue, limb, muscle, nervus, duodenum, small-bowel, pancreatic-islet-cell, and the like; as well as graft-versus-host diseases brought about by meduUa ossium transplantation. The regulation of the immune response by the compounds of the invention would also find utility in the treatment of autoimmune diseases, such as rheumatoid arthritis, systemic lupus erythematosus, Hashimoto's thyroiditis, multiple sclerosis, myasthenia gravis, type I diabetes, uveitis, allergic encephalomyeutis, glomerulonephritis, and the like; and further infectious diseases caused by pathogenic microorganisms, such as HIV. In the particular cases of HIV- 1, HIV-2 and related retroviral strains, inhibition of T-cell mitosis would suppress the replication of the virus, since the virus relies upon the host T-cell's proliferative functions to replicate.
Further uses include the treatment and prophylaxis of inflammatory and hyperproliferative skin diseases and cutaneous manifestations of immunologically-mediated illnesses, such as psoriasis, atopical dermatitis, contact dermatitis and further eczematous dermatitises, seboπhoeis dermatitis, Lichen planus, Pemphigus, bullous pemphigoid, Epidermolysis bullosa, urticaria, angioedemas, vasculitides, erythemas, cutaneous eosinophilias, Lupus erythematosus, acne, diseases or syndromes resulting in hair loss including but not limited to Alopecia areata. Further instances where a compound of the invention would be useful include various eye diseases (autoimmune and otherwise) such as keratoconjunctivitis, vernal conjunctivitis, keratitis, herpetic keratitis, conical cornea, dystrophia epithelialis comeae, corneal leukoma, ocular pemphigus, Mooren's ulcer, Scleritis, Graves' opthalmopathy, Vogt-Koyanagi-Harada syndrome, sarcoidosis, etc.; reversible obstructive airway disease, which includes conditions such as asthma (for example, bronchial asthma, aUergic asthma, intrinsic asthma, extrinsic asthma and dust asthma), particularly chronic or inveterate asthma (for example, late asthma and airway hyper-responsiveness), bronchitis and the like; inflammation of mucosa and blood vessels such as gastric ulcers, vascular damage caused by ischemic diseases and thrombosis. Moreover, hyperproUferative vascular diseases such as intimal smooth muscle cell hyperplasia, restenosis and vascular occlusion, particularly following biologically- or mechanicaUy-mediated vascular injury can be treated or prevented by the compounds of the invention.
Other treatable conditions would include but are not Umited to ischemic bowel diseases, inflammatory bowel diseases, necrotizing enterocolitis, intestinal lesions associated with thermal burns and leukotriene B4-mediated diseases; intestinal inflammations/allergies such as Coeliac diseases, proctitis, eosinophilic gastroenteritis, mastocytosis, Crohn's disease and ulcerative coUtis; food-related aUergic diseases which have symptomatic manifestation remote from the gastro-intestinal tract (e.g., migraine, rhinitis and eczema); renal diseases such as'interstitial nephritis, Goodpasture's syndrome, hemolytic-uremic syndrome and diabetic nephropathy; nervous diseases such as multiple myositis, Guillain-Barre syndrome, Meniere's disease, polyneuritis, multiple neuritis, mononeuritis and radiculopathy; endocrine diseases such as hyperthyroidism and Basedow's disease; hematic diseases such as pure red cell aplasia, aplastic anemia, hypoplastic anemia, idiopathic thrombocytopenic purpura, autoimmune hemolytic anemia, agranulocytosis, pernicious anemia, megaloblastic anemia and anerythroplasia; bone diseases such as osteoporosis; respiratory diseases such as sarcoidosis, fibroid lung and idiopathic interstitial pneumonia; skin disease such as dermatomyositis, leukoderma vulgaris, ichthyosis vulgaris, photoallergic sensitivity and cutaneous T cell lymphoma; circulatory diseases such as arteriosclerosis, atherosclerosis, aortitis syndrome, polyarteritis nodosa and myocardosis; collagen diseases such as scleroderma, Wegener's granuloma and Sjogren's syndrome; adiposis; eosinophilic fasciitis; periodontal disease such as lesions of gingiva, periodontium, alveolar bone and substantia ossea dentis; nephrotic syndrome such as glomerulonephritis; male pattern aleopecia or alopecia senilis by preventing epilation or providing hair germination and/or promoting hair generation and hair growth; muscular dystrophy; Pyoderma and Sezary's syndrome; Addison's disease; active oxygen-mediated diseases, as for example organ injury such as ischemia-reperfusion injury of organs (such as heart, Uver, kidney and digestive tract) which occurs upon preservation, transplantation or ischemic disease (for example, thrombosis and cardiac infraction): intestinal diseases such as endotoxin-shock, pseudomembranous colitis and colitis caused by drug or radiation; renal diseases such as ischemic acute renal insufficiency and chronic renal insufficiency; pulmonary diseases such as toxinosis caused by lung-oxygen or drug (for example, paracort and bleomycins), lung cancer and pulmonary emphysema; ocular diseases such as cataracta, siderosis, retinitis, pigmentosa, semle macular degeneration, vitreal scaπing and corneal alkali burn; dermatitis such as erythema multiforme, linear IgA ballous dermatitis and cement dermatitis; and others such as gingivitis, periodontitis, sepsis, pancreatitis, diseases caused by environmental pollution (for example, air pollution), aging, carcinogenis, metastasis of carcinoma and hypobaropathy; disease caused by histamine or leukotriene-C4 release; Behcet's disease such as intestinal-, vasculo- or neuro-Behcet's disease, and also Behcet's which affects the oral cavity, skin, eye, vulva, articulation, epididymis, lung, kidney and so on. Furthermore, the compounds of the invention are useful for the treatment and prevention of hepatic disease such as immunogenic diseases (for example, chronic autoimmune liver diseases such as the group consisting of autoimmune hepatitis, primary biliary ciπhosis and sclerosing cholangitis), partial liver resection, acute liver necrosis (e.g., necrosis caused by toxin, viral hepatitis, shock or anoxia), B-virus hepatitis, non-A/non-B hepatitis, cirrhosis (such as alcoholic ciπhosis) and hepatic failure such as fulminant hepatic failure, late-onset hepatic failure and "acute-on-chronic" liver failure (acute Uver failure on chronic liver diseases), and moreover are useful for various diseases because of their useful activity such as augmention of chemotherapeutic effect, preventing or treating activity of cytomegalovirus infection, particularly HCMV infection, anti-inflammatory activity, and so on.
Additionally, some compounds also possess FK-506 antagonistic properties, and are thus useful in the treatment of immunodepression or a disorder involving immunodepression. Examples of disorders involving immunodepression include AIDS, cancer, senile dementia, trauma (including wound heaUng, surgery and shock), chronic bacterial infection, and certain central nervous system disorders. The immunodepression to be treated may be caused by an overdose of an immunosuppressive macrocyclic compound, for example derivatives of 12- (2-cyclohexyl-l-methylvinyl)-13, 19,21,27-tetramethyl-l l,28-dioxa-4-azatricyclo[22.3.1.0 4 ' 9] octacos-18-ene such as FK-506, or rapamycin. Overdosing of such medicants by patients is quite common upon their reaUzing that they have forgotten to take their medication at the prescribed time and can lead to serious side effects.
A further situation in which the compounds of the present invention may be used to treat immunosuppression is in vaccination. It is sometimes found that the antigen introduced into the body for the acquisition of immunity from disease also acts as an immunosuppressive agent, and therefore antibodies are not produced by the body and immunity is not acquired. By introducing a compound of the present invention into the body (as in a vaccine), the undesired immunosuppression may be overcome and immunity acquired.
The compounds of the present invention may also find utility in the chemosensitization of drug resistant target cells. Cyclosporin A and FK-506 are known to be effective modulators of P-glycoprotein, a substance which binds to and inhibits the action of anticancer drugs; by inhibiting P-glycoprotein, they are capable of increasing the sensitivity of multidrug resistant (MDR) ceUs to chemotherapeutic agents. It is beUeved that the compounds of the invention may likewise be effective at overcoming resistance expressed to clinically useful antitumour drugs such as 5-fluorouracil, cisplatin, methotrexatε, vincristine, vinblastine and adriamycin, colchicine and vincristine.
Further, it has recently been shown that the steroid receptor-associated heat shock proteins, hsp56 or hsp59, belong to the FK506 family of immunophiUn proteins. The ability of a steroid receptor-associated heat shock protein to bind the immunosuppressive macrolide FK506 may suggest that the steroid receptor and immunophi n signal transduction pathways are functionally interrelated. The combined treatment of compounds of the present invention and low concentrations of a steroid Ugand (eg. progesterone, dexamethasone) may result in a significant enhancement of target gene expression over that seen in response to ligand alone. Thus, the compounds of the present invention may potentiate steroid-mediated transactivation.
Aqueous liquid compositions of the present invention may be particularly useful for the treatment and prevention of various diseases of the eye such as autoimmune diseases (including, for example, conical cornea, keratitis, dysophia epithelialis corneae, leukoma, Mooren's ulcer, sclevitis and Graves' ophthalmopathy) and rejection of corneal transplantation.
When used in the above or other treatments, a therapeutically-effective amount of one of the compounds of the present invention, meaning a sufficient amount of the compound to treat a particular disorder, at a reasonable benefit risk ratio, may be employed in pure form or, where such forms exist, in pharmaceutically acceptable salt, ester or prodrug form. Alternatively, the compound may be administered as pharmaceutical compositions containing the compound of interest in combination with one or more pharmaceuticaUy - acceptable excipients. It will be understood, however, that the total daily usage of the compounds and compositions of the present invention will be decided by the attending physician within the scope of sound medical judgement.
The specific therapeuticaUy-effective dose level for any particular patient wUl depend upon a variety of factors including the disorder being treated and the severity of the disorder; activity of the specific compound employed; the specific composition employed; the age, body weight, general health, sex and diet of the patient; the time of administration, route of administration, and rate of excretion of the specific compound employed; the duration of the treatment; drugs used in combination or coincidental with the specific compound employed; and like factors well known in the medical arts. For example, it is well within the skill of the art to start doses of the compound at levels lower than required to achieve the desired therapeutic effect and to gradually increase the dosage until the desired effect is achieved.
The total daily dose of the compounds of this invention administered to a human or lower animal may range from about 0.001 to about 10 mg/kg of patients body mass/day. For purposes of oral administration, more preferable doses may be in the range of from about 0.005 to about 3 mg/kg/day. If desired, the effective daily dose may be divided into multiple doses for purposes of administration; consequently, single dose compositions may contain such amounts or submultiples thereof to make up the daily dose.
The pharmaceutical compositions of the present invention comprise a compound of the invention and a pharmaceutically-acceptable earner or excipient, meaning a non-toxic solid, semi-solid or liquid filler, diluent, encapsulating material or formulation auxiliary of any type, which may be administered orally, rectally, parenterally, intracisternally, intravaginally, intraperitoneally, topically (as by powders, ointments, drops or transdermal patch), bucally, or as an oral or nasal spray. The term "parenteral" as used herein refers to modes of administration which include intravenous, intramuscular, intraperitoneal, intrasternal, subcutaneous and intraarticular injection and infusion.
Pharmaceutical compositions of this invention for parenteral injection comprise pharmaceuticaUy-acceptable sterile aqueous or nonaqueous solutions, dispersions, suspensions or emulsions, as weU as sterile powders for reconstitution into sterile injectable solutions or dispersions just prior to use. Examples of suitable aqueous and nonaqueous earners, diluents, solvents or vehicles include water, ethanol, polyols (such as glycerol, propylene glycol, polyethylene glycol, and the like), carboxymethylceUulose and suitable mixtures thereof, vegetable oils (such as olive oil), and injectable organic esters such as ethyl oleate. Proper fluidity may be maintained, for example, by the use of coating materials such as lecithin, by the maintenance of the required particle size in the case of dispersions, and by the use of surfactants.
These compositions may also contain adjuvants such as preservative, wetting agents, emulsifying agents, and dispersing agents. Prevention of the action of microorganisms may be ensured by the inclusion of various antibacterial and antifungal agents, for example, paraben, chlorobutanol, phenol sorbic acid, and the like. It may also be desirable to include isotonic agents such as sugars, sodium chloride, and the like, Prolonged absorption of the injectable pharmaceutical form may be brought about by the inclusion of agents which delay absorption, such as aluminum monostearate and gelatin.
In some cases, in order to prolong the effect of the drug, it is desirable to slow the absorption of the drug from subcutaneous or intramuscular injection. This may be accomplished by the use of a Uquid suspension of crystalline or amorphous material with poor water solubility. The rate of absorption of the drug then depends upon its rate of dissolution which, in turn, may depend upon crystal size and crystalline form. Alternatively, delayed absorption of a parenterally administered drug form is accomplished by dissolving or suspending the drug in an oil vehicle.
Injectable depot forms are made by forming microencapsule matrices of the drug in biodegradable polymers such as polylactide-polyglycolide, poly(orthoesters) and poly(anhydrides). Depending upon the ratio of drug to polymer and the nature of the particular polymer employed, the rate of drug release can be controUed. Depot injectable formulations are also prepared by entrapping the drug in liposomes or microemulsions which are compatible with body tissues.
The injectable formulations may be steriUzed, for example, by filtration through a bacterial-retaining filter, or by incorporating sterilizing agents in the form of sterile soUd compositions which can be dissolved or dispersed in sterile water or other sterile injectable medium just prior to use.
Solid dosage forms for oral administration include capsules, tablets, piUs, powders, and granules. In such solid dosage forms, the active compound is mixed with at least one inert, pharmaceutically-acceptable excipient or earner, such as sodium citrate or dicalcium phosphate and/or a) fiUers or extenders such as starches, lactose, sucrose, glucose, mannitol, and siUcic acid, b) binders such as, for example, carboxymethylceUulose, alginates, gelatin, polyvinylpyrrolidone, sucrose, and acacia, c) humectants such as glycerol, d) disintegrating agents such as agar-agar, calcium carbonate, potato or tapioca starch, alginic acid, certain sUicates, and sodium carbonate, e) solution retarding agents such as paraffin, f) absorption accelerators such as quaternary ammonium compounds, g) wetting agents such as, for example, cetyl alcohol and glycerol monostearate, h) absorbents such as kaolin and bentonite clay, and i) lubricants such as talc, calcium stearate, magnesium stearate, solid polyethylene glycols, sodium lauryl sulfate, and mixtures thereof. In the case of capsules, tablets and pills, the dosage form may also comprise buffering agents.
Solid compositions of a similar type may also be employed as fillers in soft and hard- fiUed gelatin capsules using such excipients as lactose or milk sugar as well as high molecular weight polyethylene glycols and the like.
The solid dosage forms of tablets, dragees, capsules, pills, and granules may be prepared with coatings and shells such as enteric coatings and other coatings well known in the pharmaceutical formulating art. They may optionally contain opacifying agents and can also be of a composition that they release the active ingredient(s) only, or preferentially, in a certain part of the intestinal tract, optionally, in a delayed manner. Examples of embedding compositions which can be used include polymeric substances and waxes.
The active compounds can also be in micro-encapsulated form, if appropriate, with one or more of the above-mentioned excipients.
Liquid dosage forms for oral administration include pharmaceutically-acceptable emulsions, solutions, suspensions, syrups and elixirs. In addition to the active compounds, the Uquid dosage forms may contain inert diluents commonly used in the art such as, for example, water or other solvents, solubiUzing agents and emulsifiers such as ethyl alcohol, isopropyl alcohol, ethyl carbonate, ethyl acetate, benzyl alcohol, benzyl benzoate, propylene glycol, 1,3-butylene glycol, dimethyl formamide, oUs (in particular, cottonseed, groundnut, corn, germ, oUve, castor, and sesame oUs), glycerol, tetrahydrofurfuryl alcohol, polyethylene glycols and fatty acid esters of sorbitan, and mixtures thereof.
Besides inert diluents, the oral compositions can also include adjuvants such as wetting agents, emulsifying and suspending agents, sweetening, flavoring, and perfuming agents.
Suspensions may contain, in addition to the active compounds, suspending agents as, for example, ethoxylated isostearyl alcohols, polyoxyethylene sorbitol and sorbitan esters, microcrystalline cellulose, aluminum metahydroxide, bentonite, agar-agar, and tragacanth, and mixtures thereof. Topical administration includes administration to the skin or mucosa, including surfaces of the lung and eye. Compositions for topical administration, including those for inhalation, may be prepared as a dry powder which may be pressurized or non-pressurized. In non-pressurized powder compositions, the active ingredient in finely divided form may be used in admixture with a larger-sized pharmaceutically-acceptable inert carrier comprising particles having a size, for example, of up to 100 micrometers in diameter. Suitable inert earners include sugars such as lactose. Desirably, at least 95% by weight of the particles of the active ingredient have an effective particle size in the range of 0.01 to 10 micrometers.
Alternatively, the composition may be pressurized and contain a compressed gas, such as nitrogen or a liquified gas propeUant. The Uquified propeUant medium and indeed the total composition is preferably such that the active ingredient does not dissolve therein to any substantial extent. The pressurized composition may also contain a surface active agent, such as a Uquid or soUd non-ionic surface active agent or may be a solid anionic surface active agent. It is prefeπed to use the solid anionic surface active agent in the form of a sodium salt.
A further form of topical administration is to the eye, as for the treatment of immune- mediated conditions of the eye such as automimmue diseases, allergic or inflammatory conditions, and corneal transplants. The compound of the invention is deUvered in a pharmaceuticaUy acceptable ophthalmic vehicle, such that the compound is maintained in contact with the ocular surface for a sufficient time period to allow the compound to penetrate the corneal and internal regions of the eye, as for example the anterior chamber, posterior chamber, vitreous body, aqueous humor, vitreous humor, cornea, iris/diary, lens, choroid/retina and sclera. The pharmaceuticaUy-acceptable ophthalmic vehicle may, for example, be an ointment, vegetable oil or an encapsulating material.
Compositions for rectal or vaginal administration are preferably suppositories which may be prepared by mixing the compounds of this invention with suitable non-irritating excipients or earners such as cocoa butter, polyethylene glycol or a suppository wax which are solid at room temperature but Uquid at body temperature and therefore melt in the rectum or vaginal cavity and release the active compound.
Compounds of the present invention may also be administered in the form of liposomes. As is known in the art, Uposomes are generally derived from phosphoUpids or other lipid substances. Liposomes are formed by mono- or multi-lamellar hydrated Uquid crystals that are dispersed in an aqueous medium. Any non-toxic, physiologically-acceptable and metaboUzable lipid capable of forming liposomes can be used. The present compositions in liposome form can contain, in addition to a compound of the present invention, stabiUzers, preservatives, excipients, and the like. The prefeπed lipids are the phosphoUpids and the phosphatidyl cholines (lecithins), both natural and synthetic. Methods to form liposomes are known in the art. See, for example, Prescott, Ed., Methods in Cell Biology, Volume XIV, Academic Press, New York, N.Y. (1976), p. 33 et seq.
The compounds of the invention may be prepared using one or more processes. The starting materials for use in these processes are preferably one of the macrolides isolated from culture media obtained in accordance with known methods by fermentation of microorganisms of the genus Streptomyces, which are disclosed in European Patent Application No. 0184162. Samples are avaUable from the Fermentation Research Institute, Tsukuba, Ibaraki 305, Japan under the provisions of the Budapest Treaty, under deposit No. FERM BP-927. This strain has been redeposited on April 27, 1989 with the Agricultural Research Culture CoUection Intemational Depository, Peoria, Illinois 61604, USA under the provisions of the Budapest Treaty, under deposit No. NRRL 18488. The macrolide FR- 900520 (European Patent Application 0184162), also known as ascomycin, may be prepared in accordance to the published methods of (i) H. Hatanaka, M. Iwami, T. Kino, T. Goto and M. Okuhara, FR-900520 and FR-900523, Novel immunosuppressants isolated from A streptomyces. I. Taxonomy of the producing strain. J . Antibiot., 1988. XLI(ll), 1586-1591; (ii) H. Hatanaka, T. Kino, S. Miyata, N. Inamura, A. Kuroda, T. Goto, H. Tanaka and M. Okuhara, FR-900520 and FR-900523, Novel immunosuppressants isolated from A streptomyces. II. Fermentation, isolation and physico-chemical and biological characteristics. J. Antibiot., 1988. XLI(ll), 1592-1601; (iti) T. Arai, Y. Koyama, T. Suenaga and H. Honda, Ascomycin, An Antifungal Antibiotic. J. Antibiot., 1962. 15(231-2); and (iv) T. Arai in U.S. Patent No. 3,244,592. One or more of the processes discussed below may be then employed to produce the desired compound of the invention.
Such processes comprise:
(a) producing a compound of formula I, which contains a CH-OLg group, by selective activation of a selected CH-OH group in a coπesponding compound wherein -OLg is a leaving group which is easily displaced by nucleophilic attack;
(b) producing a compound of formula I, which contains a CH-N3 group, by selective displacement of an -OLg group in a coπesponding compound;
(c) producing a compound of formula I, which contains a CH-NH2 group, by selective reduction of a CH-N3 group in a coπesponding compound;
(d) producing a compound of formula I, which contains a R'-NR"COR group, by selective acylation of a R'-NR"H group in a coπesponding compound wherein R is selected from hydrogen, aryl, arylalkyl, alkyl, Het, heterocycUc, heterocyclic-alkyl, cycloalkyl, and cycloalkylalkyl such that R' and/or R" represent(s) a radical derived from formula I; or R' and R" are R14 and R15 respectively, as defined above, and R represent(s) a radical derived from formula I; (e) producing a compound of formula I, which contains a CH-NR^2 group, by selective alkylation of a CH-NH2 group in a coπesponding compound wherein R1 and R2 are independently selected from hydrogen, aryl, arylalkyl, alkyl, heterocyclic, heterocyclic alkyl, Het, Het-alkyl, cycloalkyl, and cycloalkylalkyl;
(f) producing a compound of formula I, which contains a CH-NHC(0)NH-R14 group, by selective urea or thiourea formation from a CH-NH group in a coπesponding compound, wherein R14 is as defined above; or producing a compound of formula I, which contains a CH-NHC(O)NR14R15 group, wherein R14 an R15 are as defined above, by selective formation of a CH-N=C=O group, and addition of an amine HNR14R15;
(g) producing a compound of formula I, which contains a CH-NH-SO R group, by selective sulfonylation of a CH-NH group in a coπesponding compound wherein R is selected from aryl, arylalkyl, alkyl, cycloalkyl, cycloalkylalkyl, Het, Het-alkyl, heterocyclic alkyl and heterocycUc;
(h) producing a compound of formula I, which contains a CH-NH-C(=O)OR group, by selective carbamate formation from a selected CH-NH group in a coπesponding compound wherein R is selected from aryl, cycloalkyl, cycloalkyl alkyl, alkyl, heterocyclic alkyl, Het, Het-alkyl, heterocyclic and arylalkyl;
(i) producing a compound of formula I, which contains a CH-NH-C(=NH)NH group, by selective guanidinium formation from a CH-NH2 group in a coπesponding compound;
(j) producing a compound of formula I, which contains a CH-NH-SR group, by selective sulfenylation of a CH-NH2 group in a coπesponding compound wherein R is selected from aryl, arylalkyl, alkyl, cycloalkyl, cycloalkylalkyl, heterocyclic alkyl and Het, Het-alkyl, heterocyclic;
(k) producing a compound of formula I, which contains a CH-X group, by selective halogenation of a CH-OH group in a coπesponding compound wherein X is selected from chlorine, bromine, fluorine and iodine;
(1) producing a compound of formula I, which contains a CH-P(O)(OR) group, by selective phosphonic acid ester formation of a CH-X group in a coπesponding compound wherein R is independently selected from alkyl, arylalkyl, and aryl;
(m) producing a compound of formula I, which contains a CH-O-P(O)(OR)2 group, by selective phosphorylation of a CH-OH group in a coπesponding compound wherein R is independently selected from hydrogen, alkyl, arylalkyl, and aryl;
(n) producing a compound of formula I, which contains a CH-S-R group, by selective thioether formation from a CH-OH group in a coπesponding compound wherein R is selected from cycloalkyl, cycloalkyl alkyl, Het, Het-alkyl, heterocycUc, heterocylic alkyl, alkyl, arylalkyl, and aryl; (o) producing a compound of formula I, which contains a CH-O-C(=S)-OR group, by selective aryl- or alkyloxythiocarbonylation of a CH-OH group in a coπesponding compound wherein R is selected from cycloalkyl, cycloalkyl alkyl, Het, Het-alkyl, heterocycUc, heterocylic alkyl, alkyl, arylalkyl, and aryl;
(p) producing a compound of formula I, which contains one or more CH-O-R groups, by selective ether formation of one or more CH-OH groups in a coπesponding compound wherein R is selected from cycloalkyl, cycloalkylalkyl, Het, Het-alkyl, heterocycUc, (heterocylic)alkyl, (heterocyclic)alkenyl, (heterocyclic)alkynyl, alkyl, arylalkyl, aryl, loweralkoxycarbonylalkyl, arylalkoxycarbonylalkyl, arylalkylcarbonylalkyl, trialkylsilylcarbonylalkyl, trialkylstannylcarbonylalkyl, amidocarbonylalkyl, alkylamidocarbonylalkyl, dialkylamidocarbonylalkyl, arylamidocarbonylalkyl and heterocyclicamidocarbonylalkyl;
(q) producing a compound of formula I, which contains a CH- (substituted)phthalimide group, by selective cyclic imide formation using a CH-NH group in a coπesponding compound;
(t) producing a compound of formula I, which contains a CH2 group, by selective deoxygenation of a CH-O-C(=S)-OR group in a coπesponding compound;
(u) producing a compound of formula I, which contains a C(OH)=CH-C(=O) or a C(=O)-CH2-C(=O) group, by selective oxidation of a CH(OH)-CH2-C(=O) group in a coπesponding compound;
(v) producing a compound of formula I, which contains a C(=O)-CRιR2-C(=O) group, by selective alkylation of a C(OH)=CH-C(=O) or a C(=O)-CH2-C(=O) group in a coπesponding compound, wherein Ri and R2 are independently selected from hydrogen, aryl, cycloalkyl, cycloalkyl alkyl, alkyl, heterocyclic alkyl, Het, heterocyclic and arylalkyl, but both cannot be hydrogen;
(w) producing a compound of formula I, which contains a C(=O)-CXιX2-C(=O) group, by selective halogenation of a C(OH)=CH-C(=O) or a C(=O)-CH2-C(=O) group in a coπesponding compound wherein Xi and X2 are independently selected from fluorine, chlorine, bromine and iodine;
(x) producing a compound of formula I, which contains a C(=O)-CH(OH)-C(=O) group, by selective oxidation of a C(OH)=CH-C(=O) or a C(=O)-CH2-C(=O) group in a coπesponding compound;
(aa) producing a compound of formula I, which contains a C(=CH-R)-CH2-C(=O) group, by selective olefination of a C(OH)=CH-C(=O) or a C(=O)-CH2-C(=O) group in a coπesponding compound wherein R is selected from alkyl, aryl and arylalkyl;
(bb) producing a compound of formula I, which contains a C(OCOR)=CH-C(=O) group, by selective O-acylation of a C(OH)=CH-C(=O) or a C(=O)-CH2-C(=O) group in a coπesponding compound wherein R is selected from aryl, cycloalkyl, cycloalkyl alkyl, alkyl, heterocyclic alkyl, Het, Het-alkyl, heterocyclic and arylalkyl;
(cc) producing a compound of formula I, which contains a C(NH-R)=CH-C(=O) group, by selective amination of a C(OH)=CH-C(=0) or a C(=O)-CH2-C(=0) group in a coπesponding compound wherein R is selected from alkylamine, arylalkylamine, arylamine and amino acid derivatives;
(dd) producing a compound of formula I, which contains C(O)-C(=CH-R)-C(=O) group, by selective alkyUdene formation of a C(OH)=CH-C(=O) or a C(=O)-CH2-C(=O) group in a coπesponding compound wherein R is selected from hydrogen, aryl, cycloalkyl, cycloalkyl alkyl, alkyl, heterocyclic alkyl, Het, Het-alkyl, heterocycUc and arylalkyl;
(ee) producing a compound of formula I, which contains a carbon-carbon double bond, by elimination of HL from a coπesponding compound, where L is a leaving group;
(ff) producing a compound of formula I, which contains a quinoxaUne, benzoquinoxaline, pyrazino[2,3-d]pyridazine, pyrido[3,4-b]pyrazine, or a pteridine by condensation of a 1,2-dicarbonyl or masked 1,2-dicarbonyl groups of a coπesponding compound with an appropriate aromatic diamine;
(gg) producing a compound of formula I, which contains one or more hydroxyl groups, by selective reduction of one or more C=O groups of a coπesponding compound;
(hh) producing a compound of formula I, which contains one dihydro- benzo[l,5]thiazepine, by reaction of an alpha,beta-unsaturated ketone of a coπesponding compound with an appropriate 2-aminothiophenol;
(ii) producing a compound of formula I, which contains one or more carbonyl groups, by selective oxidation of one or more hydroxyl groups of a coπesponding compound;
(jj) producing a compound of formula I, by selective reaction of one of the carbonyl groups of a coπesponding compound and dithiols;
(kk) producing a compound of formula I, which contains an oxime group, by selective reaction of one of the carbonyl groups of a coπesponding compound with hydroxyl amine or O-alkylated hydroxyl amines;
(11) producing a compound of formula I, which contains a pyrazole system, by condensation of a 1,3-dicarbonyl group of a coπesponding compound and appropriate hydrazines;
(mm) producing a compound of formula I, which contains a substituted pyrimidine system, by condensation of the 1,3-dicarbonyl group of a coπesponding compound with appropriate amidines, guanidines, isoureas, ureas and thioureas;
(nn) producing a compound of formula I, which contains a furan system, by reaction of the 1,3-dicarbonyl group of a coπesponding compound with appropriate diazoacetic esters or diazomethyl ketones; (oo) producing a compound of formula I, which contains an isoxazole system, by condensation of the 1,3-dicarbonyl group of a coπesponding compound with hydroxyl amine;
(pp) producing a compound of formula I, which contains a pyridine system, by condensation of the 1,3-dicarbonyl group of a coπesponding compound with appropriate malonic acid derivatives or cyanoacetic acid derivatives;
(qq) producing a compound of formula I, which contains a benzo[l,5]thiazepine, benzo[l,5]oxazepine or benzo[l,5]diazepine system, by condensation of the 1,3-dicarbonyl group of a coπesponding compound with appropriate 2-aminothiophenols, 2-aminophenols, and 1,2-aromatic diamines;
(π) producing a compound of formula I, which contains a keto-substituted furan system, by reaction of the 1,3-dicarbonyl group of a coπesponding compound with appropriate aldehydes, and enol ethers;
(ss) producing a compound of formula I, which contains a substituted phenyl group, by C-arylation of a 1,3-dicarbonyl group of a coπesponding compound with appropriate 1- halo-2-nitro-aromatics;
(uu) producing a compounds of formula I, which contains a 2-isoxazoUne, by nitrile oxide 1,3-dipolar cycloaddition to an enone;
(zz) producing a compound of formula I, which contain either a beta-hydroxy ketone or an alpha,beta-enone, by reductive hydrolysis of a coπesponding 2-isoxazoline and subsequent separation of the two compounds;
(eee) producing a compound of formula I, which contains a hydrazone, by selective hydrazone formation with a coπesponding ketone;
(hhh) producing a compound of formula I, which contains an aUylic alcohol, by selective reduction of a coπesponding enone;
(in) producing a compound of formula I, which contains an epoxide, by selective addition of the carbene arising from diazomethane across an activated carbonyl;
(jjj) producing a compound of formula I, which contains a carboxylic acid, by selective ester cleavage in a coπesponding compound;
(kkk) producing a compound of formula I, which contains a substituted or unsubstituted carboxamide, by selective condensation of the coπesponding amine with a coπesponding carboxyUc acid;
(1U) producing a compound of formula I, which contains a 24R-hydroxyl substituent, by selective inversion of the naturally occurring 24S configuration;
(mmm) producing a compound of formula I, which contains an alkyloxycarbonyl hydrazone, by selective condensation of an alkyl carbazate with a coπesponding compound of formula I, having a ketone; (PPP) producing a compound of formula I, which contains one thiazole, by condensation of an alpha substituted carbonyl or an alpha substituted masked carbonyl group of a coriesponding compound with an appropriate thioamide, thiourea or with dithiocarbamic acid derivatives, where the alpha substituent L is a leaving group;
(qqq) producing a compound of formula I, which contains one imidazole, by condensation of an alpha substituted carbonyl or an alpha substituted masked carbonyl group of a coπesponding compound with an appropriate amidine, isourea or guanidine, where the substituent L is a leaving group;
(rπ) producing a compound of formula I, which contains one oxazole, by condensation of an alpha substituted carbonyl or an alpha substituted masked carbonyl group of a coπesponding compound with an appropriate amide, where the substituent L is a leaving group;
(sss) producing a compound of formula I, which contains a tertiary alcohol, by selective addition of a Grignard reagent or an organometallic reagent to a carbonyl moiety of a coπesponding compound;
(ttt) producing a compound of formula I, which contains one pyπole, by cyclization of an appropriate gamma-amino alpha hydroxy carbonyl or a masked gamma-amino alpha hydroxy carbonyl of a coπesponding compound prepared by process (sss);
(uuu) producing a compound of formula I, which contains one pyrazine, by condensation of a 1,2-dicarbonyl or masked 1,2-dicarbonyl group of a coπesponding compound with an appropriate 1,2-diamine in the presence of an oxidizing agent;
(vvv) producing a compound of formula I, which contains one pyridine, by condensation of a 1,5-dicarbonyl group prepared by process (sss) of a coπesponding compound with ammonia;
(www) producing a compound of formula I, which contains one pyridazine, by condensation of a 1,4-dicarbonyl group prepared by process (sss) of a coπesponding compound with hydrazine;
(xxx) producing a compound of formula I, which contains a 1,2-thiocarbonate, by reacting a 1,2-diol of a coπesponding compound with thiocarbonyldiimidazole or an appropriately activated thiocarbonate;
(yyy) producing a compound of formula I, which contains a 1,2-carbonate, by reacting a 1,2-diol of a coπesponding compound with carbonyldiimidazole, triphosgene, phosgene or an appropriately activated carbonate;
(zzz) producing a compound of formula I, which contains a 1,2-phosphonate group, by reacting a 1,2-diol of a coπesponding compound with an appropriate alkoxyphosphonyl dichloride;
(aaaa) producing a compound of formula I, which contains an olefin, by reduction of a 1,2-thiocarbonate prepared by process (xxx) of a coπesponding compound; (bbbb) producing a compound of formula I, which contains a CH2 group, by selective reduction of a 1,2-dicarbonyl or masked 1,2-dicarbonyl group of a coπesponding compound;
(cccc) producing a compound of formula I, which contains an indole group, by selective reduction and condensation of a 2-(o-nitrophenyl)-l,3-diketone [prepared by process (ss)] of a coπesponding compound;
(dddd) producing a compound of formula I, which contains a substituted triazole group, by cycloaddition of a CH-N3 group in a coπesponding compound with appropriate acetylene analogues;
(eeee) producing a compound of formula I, which contains a substituted pyπole group, by reaction of a CH-NH2 group in a coπesponding compound with appropriate dicarbonyl compounds;
(ffff) producing a compound of formula I, which contains one ethanalyl group, first by selective oxidation of the double bond of an allyl group to a vicinal diol, followed by oxidative cleavage of the diol in a coπesponding compound;
(gggg) producing a compound of formula I, which contains one carboxymethyl group, by selective oxidation of an ethanalyl group in a coπesponding compound;
(hhhh) producing a compound of formula I, which contains one alkyl carboxymethyl group, by esterification of a carboxymethyl group in a coπesponding compound;
(iui) producing a compound of formula I, which contains one cyclopropylmethyl group, by selective cyclopropanation of the double bond of an allyl group in a coπesponding compound;
(jjjj) producing a compound of formula I, which contains one pyπole, by reaction of a 1,4-dicarbonyl group with amines in a coπesponding compound;
(kkkk) producing a compound of formula I, which contains one furan, by cyclization of a 1,4-dicarbonyl group in a coπesponding compound;
(1111) producing a compound of formula I, which contains one methyl ketone, by selective oxidation of the double bond of an allyl group in a coπesponding compound;
(nnnn) producing a compound of formula I, which contains a hydrazide, by reduction of the coπesponding hydrazone;
(oooo) producing a compound of formula I, which contains an amine, by reduction of the coπesponding oxime;
(PPPP) producing a compound of formula I, which contains an alpha,beta-saturated ketone, by reduction of the coπesponding alpha,beta-unsaturated enone;
(qqqq) producing a compound of formula I, which contains an isoxazoline, by treatment of a beta-hydroxy oxime with a dehydrating reagent;
(ππ) producing a compound of formula I, which contains an beta-hydroxy carbonyl, by treatment of a carbonyl with a base in the presence of another carbonyl moiety; (ssss) producing a compound of formula I, which contains a cycUc imine, by treatment of an enone system with a glycine imine in the presence of base resulting in first Michael addition at the beta-carbon and subsequent imine formation upon aqueous workup;
(tttt) producing a compound of formula I, which contains a substituted pyπole, by treatment of an enone with a glycine imine in the presence of an appropriate catalyst to induce a 1,3-dipolar cycloaddition;
(uuuu) producing a compound of formula I, which contains a beta-keto carbox-ylic acid, ester or amide, by decomposition with light or heat of an alpha diazoketone;
(vvvv) producing a compound of formula I which contains a ketone, a product of decarboxylation of a beta-keto carboxylic acid, by heating;
(yyyy) producing a compound of formula I, which contains a -CHOC(O)OR400, by selective mod-aryl-, mod-Het-, or alkyloxy-carbonylation of a -CHOH group in a coπesponding compound;
(zzzz) producing a compound of formula I, which contains an aUylic hydroxyl group, by selective oxidation of an allylic methylene group in a coπesponding compound.
In process (a), suitable reagents for activation of an alcohol include acetic anhydride, trifluoromethanesulfonic anhydride (triflic anhydride), methanesulfonyl chloride (mesyl chloride), /.-toluenesulfonyl chloride (tosyl chloride), trifluoroacetic anhydride, trifluoroacetyl chloride, methoxysulfonyl fluoride (magic methyl), o-nitrobenzenesulfonyl chloride, l-methyl-2-fluoropyridinium salt and the like.
The activation may be carried out in a solvent which does not adversely affect the reaction (e.g., diethylether, dichloromethane, tetrahydrofuran, chloroform or NN- dimethylformamide or a mixture thereof). The reaction may require cooling or heating, depending on the activation method chosen. Further, the reaction is preferably conducted in the presence of an organic or inorganic base such as an alkaUne earth metal (e.g. calcium, etc.), alkali metal hydride (e.g. sodium hydride, etc.), alkaU metal hydroxide (e.g. sodium hydroxide, potassium hydroxide, etc.), alkaU metal carbonate (e.g. sodium carbonate, potassium carbonate, etc.), alkaU metal hydrogen carbonate (e.g. sodium hydrogen carbonate, potassium hydrogen carbonate, etc.), alkaU metal alkoxide (e.g. sodium methoxide, sodium ethoxide, potassium tert-butoxide, etc.), alkali metal alkanoic acid (e.g. sodium acetate, etc.), tiialkylamine (e.g. triethylamine, etc.), pyridine compounds (e.g. pyridine, lutidine, picoline, 4-N,N-dimethylaminopyridine, etc.), quinoline, and the like, preferably in the presence of organic bases such as triethylamine or pyridine.
The activation may also be caπied out using a starting material having an opposite configuration at a carbon center. In this situation, the following two additional steps are required to yield a starting material having an epimeric hydroxyl moiety, i.e. (1) the alcohol is oxidized to its coπesponding ketone, (2) the obtained ketone is reduced under selective conditions. Both chiral centers having either [Rj- or [S] -configuration can be obtained selectively and separately.
In process (b), suitable azide reagents include well-estabUshed alkali metal azides such as sodium or Uthium azides (NaN3 or L1N3) in the presence or absence of crown ethers, more reactive tetraalkylammonium azides (Danishefski, S. J.; DeNinno, M. P.; Chen, S.-H. J. Am. Chem. Soc. 1988, 110, 3929), tetramethylguanidinium azide, (Papa, A. J. J. Org. Chem. 1966, 31, 1426), a copper-assisted azide reaction (Yamamoto, Y.; Asao, N. /. Org. Chem. 1990, 55, 5303) and a hydrogen azide-amine system (Saito, S.; Yokoyama, H.; Ishikawa, T.; Niwa, N.; Moriwake, T. Tetrahedron Lett. 1991, 32, 663; Saito, S.; Takahashi, N.; Ishikawa, T.; Moriwake, T. Tetrahedron Lett. 1991, 32, 667). The azide displacement reaction may be caπied out in a solvent which does not adversely affect the reaction (e.g. chloroform, dichloromethane, tetrahydrofuran, pyridine, dimethylsulfoxide, NN-dimethylformamide, hexamethylphosphoramide, etc. or a mixture thereof). The reaction may be conducted above, at, or below ambient temperature.
In process (c), the reduction may be carried out catalytically using hydrogen. Suitable catalysts include, but are not limited to platinum catalysts (e.g. platinum oxide, platinum black), palladium catalysts (e.g. palladium oxide, paUadium on charcoal, palladium black, palladium hydroxide on charcoal, palladium on calcium carbonate poisoned with lead, palladium on barium carbonate with quinoline), nickel catalysts (e.g. nickel oxide, Raney nickel), rhodium catalysts (e.g. rhodium on alumina). Reduction may also be carried out using metal reducing reagents (see Review; Scriven, E. F. V.; Turnbull, K. Chem Rev. 1988, 88, 321; Patai, S., Ed., "The Chemistry of the Azido Group," Interscience Publishers, New York, 1971; Scriven, E. F. V., Ed., "Azides and Nitrenes Reactivity and Utility," Academic Press, Inc., New York, 1984) such as sodium borohydride under phase- transfer conditions, borohydride supported on an ion exchange resin, lithium aluminum hydride and the like, furthermore, 1,3-propanedithiol-triethylamine method (Bayley, H.; Staudring, D. N.; Knowles, J. R. Tetrahedron Lett. 1978, 3633), triphenylphosphine (Vaultier, M.; Knouzi, N.; Caπie, R. Tetrahedron Lett. 1983, 24, 763), and sodium tellurium hydride (Suzuki, H.; Takaoka, K. Chem Lett. 1984, 1733).
The reduction may be carried out in a solvent which does not adversely affect the reaction (e.g., alcohols, water, acetone, dichloromethane, tetrahydrofuran, pyridine or NN- dimethylformamide or a mixture thereof). The reaction may be conducted above, at, or below ambient temperature.
In process (d), suitable N-acylations may be carried out using the methods of symmetric carboxylic acid anhydrides, carboxylic acid halides, mixed carbonic-carboxylic anhydrides, active esters (p-nitrophenylester, trichlorophenyl ester, pentafluorophenyl ester, N-hydroxysuccinimide, cyanoethyl, 2,2,2-trichloroethyl and the like), and carboxylic acid with suitable condensing reagents such as DCC (N,N-dicyclohexylcarbodiimide and its related condensing agents), DCC-HOBt (NN-dicyclohexylcarbodiimide-1- hydroxybenzotriazole), Woodward reagent K method, NJV-carbonyldiimidazole and phosphonium containing reagents (e.g. benzotriazolyloxytris[dimethylamino]-phosphonium hexafluorophosphate, NN-bis[2-oxo-3-ox-azolidinyl]phosphorodiamidic chloride, diethylphosphorobromidate, diphenylphosphoryl azide, bromo tris[dimethylamino]phosphonium hexafluorophosphate, and the like). Suitable reagents for amide formation include, but are not limited to formyl derivatives, acetyl halides (chloroacetyl, trichloroacetyl, σ-nitrophenylacetyl, o-nitrophenoxyacetyl, acetoacetyl, [N'-dithiobenzyloxycarbonylaminojacetyl and the like), and substituted propionyl derivatives (3-phenylpropionyl, isobutyryl, picoUnoyl, and the like). Other groups may be found in volume 3 of The Peptides Gross, E. and Meinhofer, J. Academic Press, 1981 and Protective Groups in Organic Synthesis Greene, T. W. John WUey & Sons, New York, Chapter 7, 1981. Typically used coupling conditions are described by Gross, E.; Meinhofer, J. "The Peptides" vol. 3, Academic Press, 1981. The N-acylation may be carried out in a solvent which does not adversely affect the reaction (e.g. acetone, dichloromethane, chloroform, tetrahydrofuran, NN-dimethylformamide, dimethylsulf oxide, diethylether, and the like, or a mixture thereof). The reaction may be conducted above, at, or below ambient temperature. Alternatively, metal salts may be formed from the desired amines and then condensed with an ester which may or may not be activated. These salts may be formed by treatment of the neutral amine with trialkylaluminums (See J. I. Levin, E. Turos, S. M. Weinreb Synthetic Communications 1982, 12, 989-93), Sn[Ν(Si(CH3)3)]2 (See W. Wang, E. J. Roskamp /. Org. Chem. 1992, 57, 6101-3), or grignard reagents. For other methods see A. SoUadie-Cavallo, M. Bencheqroun J. Org. Chem. 1992, 57, 5831-4 as well as footnotes 2, 3, 4, 5, 6 and 7 therein.
In process (e), N-alkylations may be carried out using aldehydes or ketones-foUowed by reduction of the initiaUy formed iminium ion {The following reagents can be used for the reduction; sodium cyanoborohydride-boron trifluoride or the reducing reagents cited in process (c)}, coπesponding halides in the presence of bases Usted in process (a), or lithium dialkyl cuprate (King, F. E.; King, T. J.; Muir, I. H. M. J. Chem. Soc. 1946, 5; Yamamoto, H.; Maruoka, K. J. Org. Chem. 1980, 45, 2739). Suitable reagents for N-alkylation include, but are not Umited to benzyl halide, 3,4-dimethoxybenzyl haUde, nitrobenzyl halide, di(p- methoxyphenyl)methyl halide, triphenylmethyl halide, and the like. Other groups may be found in volume 3 of The Peptides, Gross, E. and Meinhofer, J. Academic Press, 1981 and Protective Groups in Organic Synthesis, Greene, T. W. John Wiley & Sons, New York, Chapter 7, 1981. The N-alkylation may be caπied out in a solvent which does not adversely affect the reaction (e.g., acetone, dichloromethane, tetrahydrofuran, pyridine or NN- dimethylformamide or a mixture thereof). The reaction may be conducted above, at, or below ambient temperature. In process (f), urea formation may be caπied out from the following reactions; reaction with silicon tetraisocyanate or sUicon tetraisothiocyanate (NeviUe, R. G.; McGee, J. J. Can. J. Chem. 1963, 41, 2123), reaction with NN-carbonyldiimidazole or NN- thiocarbonyldiimidazole, foUowed by N-substituted primary or secondary amines or ammonia (Staab, H. A.; Wendel, K. Org. Synth. 1968, 48, 44), and reaction with phosgene or thiophosgene in the presence of tert-amine, followed by N-substituted primary or secondary amines or ammonia. The ureido formation may be carried out in a solvent which does not adversely affect the reaction (e.g. acetone, toluene, dichloromethane, tetrahydrofuran, pyridine, NN-dimethylformamide, etc. or a mixture thereof). The reaction may be conducted above, at, or below ambient temperature.
Alternatively, urea formation may be caπied out by first forming an acyl azide by activating a carboxyUc acid in the molecule with a chloroformate, such as isobutyl chloroformate, in the presence of a tertiary amine, such as Ν-methyl-morpholine or Ν- methyl-piperidine, and treating with an azide source, such as sodium azide, hydrazoic acid, trimethylsilylazide, or tetramethylguanidinium azide. The acyl azide may also be formed directly using diphenylphophorylazide in the presence of a tertiary amine. The reaction mixture is then heated at from 40 °C to 100 °C for 0.5 to 6 hours, whereupon the amine HΝR14R15 is added at a temperature at from 23 °C to 100 °C. The reaction is conducted in an inert organic solvent such as diethyl ether, tetrahydrofuran, 1,4-dioxane, chloroform, methylene chloride, benzene, or toluene.
In process (g), N-sulfonylation may be caπied out using substituted sulfonylhaUdes in the presence of suitable tert-amines such as tiialkylamine, pyridine, and the like (Remers, W. A.; Roth, R. H.; Gibs, G. J.; Weiss, M. J. J. Org. Chem. 1971, 36, 1232). Suitable reagents include, but are not Umited to benzenesulf onyl haUde, p-methyoxybenzenesulf onyl haUde, 2,4,6-trimethylbenzenesulf onyl haUde, toluenesulfonyl haUde, benzylsulf onyl halide, p- methoxybenzylsulfonyl haUde, trifluoromethylsulfonyl haUde, phenacylsulfonyl halide, and the like. Some other representative groups may be found in volume 3 of The Peptides, Gross, E. and Meinhofer, J. Academic Press, 1981 and Protective Groups in Organic Synthesis, Greene, T. W. John Wiley & Sons, New York, Chapter 7, 1981. The N-aryl- or -dkylsulfonylation may be carried out in a solvent which does not adversely affect the reaction (e.g., acetone, dichloromethane, tetrahydrofuran, pyridine or NN- dimethylformamide or a mixture thereof). The reaction may be conducted above, at, or below ambient temperature.
In process (h), N-carbamate formations may be caπied out using common protecting groups for amino group such as, but not Umited to methylcarbamates (cyclopropylmethyl, 9- fluorenylmethyl, and the like), substituted ethylcarbamates (2,2,2-trichloroethyl, 2- phosphonoethyl, 2-methylthioethyl, and the like), substituted propyl and isopropylcarbamates (1,1-dimethylpropynyl, 1 -methyl- l-(4-biphenylyl)ethyl, tert-butyl, phenyl, p-nitrobenzyl, 8- quinolyl, N-hydroxypiperidinyl, benzyl, dimethoxybenzyl, 9-anthrylmethyl, 1-adamantyl, cyclohexyl, tert-amyl, cinnamoyl, isobutyl, N'-p-phenylaminothiocarbonyl, N- piperidinylcarbonyl, diphenylmethyl, and the like). Preparations of N-carbamates and other groups may be found in volume 3 of The Peptides, Gross, E. and Meinhofer, J. Academic Press, 1981 and Protective Groups in Organic Synthesis, Greene, T. W. John Wiley & Sons, New York, Chapter 7, 1981. The N-carbamate formation may be carried out in a solvent which does not adversely affect the reaction (e.g., acetone, dichloromethane, tetrahydrofuran, pyridine or NN-dimethylformamide or a mixture thereof). The reaction may be conducted above, at, or below ambient temperature.
In process (i), N-guanidium formation may be caπied out using several common reagents such as l-guanyl-3,5-dimethylpyrazole (Salvadori, S.; Sarto, G. P.; Tomatis, R. Eur. J. Med. Chem. Chim. Ther. 1983, 18, 489), O-methylisourea (Van Νispen, J. W.; Tesser, G. I.; Νivard, R. J. F. Int. J. Peptide Protein Res. 1977, 9, 193), and thiourea sulf onylate (Maryanoff, C. A.; Stanzione, R. C; Plampin, J. Ν.; Mills, J. E. J. Org. Chem. 1986, 57, 1882). The N-guanidinium formation may be carried out in a solvent which does not adversely affect the reaction (e.g., acetone, dichloromethane, tetrahydrofuran, pyridine or NN-dimethylformamide or a mixture thereof). The reaction may be conducted above, at, or below ambient temperature.
In process (j), N-sulfenamides may be prepared from an amine and a sulfenyl halide (Davis, F. A.; Nadir, U. K. Org. Prep. Proc. Int. 1979, 11, 33; Kobayashi, T.; lino, K.; Hiraoka, T. /. Am. Chem. Soc. 1977, 99, 5505; Zervas, L.; Borovas, D.; Gazis, E. J. Am. Chem. Soc. 1963, 85, 3660). Suitable reagents include, but are not Umited to benzenesulfenyl halide, o-nitrobenzenesulfenyl halide, 2,4-dinitrosulfenyl halide, pentachlorobenzenesulfenyl halide, 2-nitro-4-methoxybenzenesulfenyl halide, triphenylmethylsulfenyl hatide, and the like. Other groups may be found in volume 3 of The Peptides, Gross, E. and Meinhofer, J. Academic Press, 1981 and Protective Groups in Organic Synthesis, Greene, T. W. John Wiley & Sons, New York, Chapter 7, 1981. The N-sulfenylation may be carried out in a solvent which does not adversely affect the reaction (e.g., acetone, dichloromethane, tetrahydrofuran, pyridine or NN-dimethylformamide or a mixture thereof). The reaction may be conducted above, at, or below ambient temperature.
In process (k), suitable halogenation reagents include, but are not Umited to triphenylphosphine with halogens (Verheyden, J. P. H.; Moffatt, J. G. /. Am. Chem. Soc. 1964, 86, 2093; Bergman, R. G. ibid., 1969, 91, 7405; Hrubiec, R. T.; Smith, M. B. /. Org. Chem., 1983, 48, 3667), triphenylphosphine with cyanogen halides (Homer, L.; Oediger, H.; Hoffmann, H. Annalen Chem. 1959, 626, 26), triphenylphosphine with carbon tetrahalides (Hooz, J.; Gilani, S. S. H. Can. J. Chem. 1968, 46, 86; Chem. Commun. 1968, 1350), triphenylphosphine with ΝBS (N-bromosuccinimide)(Schweizer, E. E.; Creasy, W. S.; Light, K. K.; Shaffer, E. T. J. Org. Chem. 1969, 34, 212), and triphenylphosphine with hexachloroacetone (Magid, R. M.; Stanley-Fruchey, O.; Johnson, W. L. Tetrahedron Lett. 1977, 2999; Magnid, R. M.; Stanley-Fruchey, O.; Johnson, W. L.; AUen, T. G. J. Org. Chem. 1979, 44, 359). The halogenation may also be accompUshed by other reagents such as mono- or tri-alkylsUyl halides with or without sodium halides (Olah, G. A.; Husain, A.; Singh, B. P.; Mehrota, A. K. /. Org. Chem. 1983, 48, 3667; Balme, G.; Fournet, G.; Gore, J. Tetrahedron Lett. 1986, 27, 1907), polymer bound trimethylsilyl derivatives (CainelU, G.; Contento, M.; Manescalchi, F.; Plessi, L.; Panunzio, M. Synthesis 1983, 306; Imamoto, T.; Matsumoto, T.; Kusumoto, T.; Yokoyama, M. Synthesis 1983, 460), NN-dichlorophosphoramidic dichloride (Chem. Lett. 1978, 923), phosphorus trihalide-zinc halide (Anderson, Jr. A. G.; Owen, Ν. E. T.; Freenor, F. J.; Erickson, D. Synthesis 1976, 398), diethylaminosulfur trifluoride (Middleton, W. J. J. Org. Chem. 1975, 40, 574), triphenoxyphosphonium alkyl halide (Rydon, H. Ν. Org. Synth. 1971, 57, 44; Verheyden, J. P. H.; Moffatt, J. G. /. Org. Chem. 1972, 37, 2289), and the like.
The halogenation may be caπied out in a solvent which does not adversely affect the reaction (e.g., acetone, dichloromethane, tetrahydrofuran, pyridine or NN- dimethylformamide or a mixture thereof). The reaction may be conducted above, at, or below ambient temperature.
In process (1), phosphonic acid ester formation may be caπied out using Michaelis- Arbuzov reactions (Bhattacharya, A. K.; Thyagarajan, G. Chem. Rev. 1981, 81, 415; Bauer, G.; Haegele, G. Angew. Chem. Int. Ed. Engl. 1977, 16, 477).
The phosphonic acid ester formation may be carried out in a solvent which does not adversely affect the reaction (e.g., acetone, dichloromethane, tetrahydrofuran, pyridine or NN-dimethylformamide or a mixture thereof). The reaction may be conducted above, at, or below ambient temperature.
In process (m), phosphorylation may be carried out using, but is not Umited to the 2- halo-2-oxo- 1, 3, 2-dioxaphospholane-triethylamine reaction (Chandrarakumar, Ν. S.; Hajdu, J. J. Org. Chem. 1983, 48, 1197). The phosphorylation may be carried out in a solvent which does not adversely affect the reaction (e.g., benzene, toluene, acetone, dichloromethane, tetrahydrofuran or N,N-dimethylformamide or a mixture thereof). Further, the reaction is preferably conducted in the presence of organic or inorganic bases, as described in process (a), preferably in the presence of organic bases such as triethylamine, pyridine etc. The reaction may be conducted above, at, or below ambient temperature, more preferably from 0 to 50 °C.
In process (n), thioether formation may be caπied out using, but is not limited to aryl- or alkylmercaptan in the presence of suitable tert-amines such as tiialkylamine, pyridine, and the like. The reaction may also be carried out by a metal-catalyzed thioether formation (Guindon, Y; Frenette, R; Fortin, R.; Rokach, J. J. Org. Chem. 1983, 48, 1357), alkali metal salts of aryl- or alkylmercaptans with a compound of formula I which contains CH-OLg group (OLg is the leaving group). The alkali metal may be selected from sodium, potassium, lithium, and cesium. The thioether formation may be caπied out in a solvent which does not adversely affect the reaction (e.g. acetone, dichloromethane, tetrahydrofuran, pyridine, NN- dimethylformamide, etc. or a mixture thereof). The reaction may be conducted above, at, or below ambient temperature.
In process (o), aryl- or alkyloxythiocarbonylation may be carried out using aryl- or alkyloxythiocarbonylchloride or coπesponding halides in the presence of suitable tert-amines such as tiialkylamine, pyridine, and the like. The aryl- or alkylthiocarbonylation may be caπied out in a solvent which does not adversely affect the reaction (e.g. acetone, dichloromethane, tetrahydrofuran, pyridine, NN-dimethylformamide etc. or a mixture thereof). The reaction may be conducted above, at, or below ambient temperature.
In process (p), ether formation may be caπied out using, for example, aryl-, arylalkyl- , (heterocyclic)alkyl-, (heterocyclic)alkenyl-, (heterocyclic)alkynyl-, loweralkoxycarbonylalkyl-, arylalkoxycarbonylalkyl-, arylalkylcarbonylalkyl-, trialkylsilylcarbonylalkyl-, trialkyl-stannylcarbonylalkyl-, amidocarbonylalkyl-, alkylamidocarbonylalkyl-, dialkylamido-carbonylalkyl-, arylamidocarbonylalkyl-, alkylamidocarbonylalkyl-, heterocyclicamido-carbonylalkyl-, heterocycUc or alkylhalides in the presence of KY-zeoUte (Onaka, M.; Kawai, M.; Izumi, Y. Chem. Lett. 1983, 1101), polymeric materials (Kimura, Y.; Kirszensztejn, P.; Regen, S. L. J. Org. Chem. 1983, 48, 385), nickel-catalysis (Camps, F.; Coll, J.; Moreto, J. M. Synthesis 1982, 186; Yamashita. Synthesis 1977, 803), arylalkyl-O-p-toluenesulfonate (Dewick, P. M. Synth. Commun. 1981, 77, 853), potassium or sodium alkoxides (Bates, R. B.; Janda, K. D. /. Org. Chem. 1982, 47, 4374), pyridine or other bases (Chem. Lett. 1978, 57), tetraalkylammonium halide (Miller, J. M.; So, K. H.; Clark, J. H. Can. J. Chem. 1979, 1887), mercury perchlorate (McKiUop, A.; Ford, M. E. Tetrahedron 1974, 30, 2467), silver triflate or silver oxide (Kuhn, R.; Low, I.; Trischmann, H. Chem. Ber. 1957, 90, 203. Croon, I.; Lindberg, B. Acta Chem. Scand., 1959, 13, 593) or a phase transfer catalyst (McKiUop, A.; Fiaud, J.-C; Hug, R. P. Tetrahedron 1974, 30, 1379). The ether formation may also be carried out with dialkyl- or diarylphosphoric acid in the presence of p-toluenesulfonic acid (Kashman, Y. J. Org. Chem. 1972, 37, 912), with diazo compounds with tin(E) chloride (Christensen, L. F.; Broom, A. D. J. Org. Chem. 1972, 37, 3398), or with 2,2,2-trichloroalkanols in the presence of base (Corey, E. J.; Link, J. O. J. Am. Chem. Soc. 1992, 114, 1906; Corey, E. J.; Link, J. O. Tetrahedron Lett. 1992, 33, 3431). Additionally, ether formation may be accomplished with a suitable trichloroacetimidate in the presence of an acid catalyst (Wessel, H. P.; Iversen, T.; Bundle, D. R. J. Chem. Soc. Perk Trans. 1985, 7, 2247.) The ether formation may be carried out in a solvent which does not adversely affect the reaction (e.g. acetone, dichloromethane, tetrahydrofuran, pyridine, NN-dimethylformamide, ether, cyclohexane, etc. or a mixture thereof). The reaction may be conducted above, at, or below ambient temperature. More specifically, O-alkylation may be carried out using bromoacetic acid derivatives, iodoacetic acid derivatives, trifluoromethanesulfonyloxy acetic acid derivatives, chloro- bromo- or iodomethanesulfonic acid derivatives, chloro- bromo- or iodoacetyltrimethylsUane and the like in the presence of an appropriate base such as triethylamine, potassium fluoride or silver(I) oxide. The reaction is performed in an inert solvent such as N,N-dimethylformamide, acetonitrile or dichloromethane, preferably between -50 °C and 80 °C. Alternatively, alkylation can be carried out using alkyl-, or arylalkyl- diazoacetates in the presence of a metal catalyst, for example Rh(OAc)2 in an inert solvent such as dichloromethane preferably between -20 °C and 80 °C.
In process (q), N-cyclic imide formations may be carried out using phthalic anhydride (Sasaki, T.; Minamoto, K.; Itoh, H. J. Org. Chem. 1978, 43, 2320), o -methoxycarbonyl- benzoyl chloride with trialkylamine (Hoogwater, D. A.; Reinhoudt, D. Ν.; Lie, T. S.; Gunneweg, J. J.; Beyerman, H. C. Reel. Trav. Chim. Pays-Bas. 1973, 92, 819), orN- ethoxycarbonylphthalimide (Νefkens, G. H. L.; Tesser, G. I.; Νivard, R. J. F. Reel. Trav. Chim. Pays-Bas. 1960, 79, 688). Other groups and reagents may be found in volume 3 of The Peptides, Gross, E. and Meinhofer, J. Academic Press, 1981 and Protective Groups in Organic Synthesis, Greene, T. W. John WUey & Sons, New York, Chapter 7, 1981. The N- cyclic imide formation may be caπied out in a solvent which does not adversely affect the reaction (e.g. acetone, dichloromethane, tetrahydrofuran, pyridine, NN-dimethylformamide, etc. or a mixture thereof). The reaction may be conducted above, at, or below ambient temperature.
In process (t), deoxygenation may be carried out using, but is not Umited to phenoxythiocarbonyl derivative with tributyltin hydride and 2,2-azobis-2-methylpropionitrile (AIBΝ) (Robins, M. J.; Wilson, J. S.; Hansske, F. J. Am. Chem. Soc. 1983, 705, 4059; Barton, D. H. R.; McCombie, S. W. J. Chem. Soc, Perkin Trans.l 1975, 1574), or a phenyldithiocarbonyl derivative with tributyltin hydride and AIBΝ (Hayashi, T.; Iwaoka, T.; Takeda, Ν.; Ohki, E. Chem. Pharm. Bull. 1978, 26, 1786). The deoxygenation may be caπied out in a solvent which does not adversely affect the reaction (e.g. acetone, dichloromethane, tetrahydrofuran, pyridine, NN-dimethylformamide, etc. or a mixture thereof). The reaction may be conducted above, at, or below ambient temperature.
In process (u), suitable oxidizing reagents, include activated dialkyl sulfoxides (e.g. dimethylsulfoxide, methylethylsulfoxide) (Mancuso, A. J.; Swem, D. Synthesis 1981, 165), organo chromates [e.g. pyridinium chlorochromate (Corey, E. J.; Suggs, J. W. Tetrahedron Lett. 1975, 2647; Corey, E. J.; Boger, D. L. Tetrahedron Lett. 1978, 2461), pyridinium dichromate (Corey, E. J.; Schmidt, G. Tetrahedron Lett. 1979, 5, 399), Collins reagent (Collins, J. C; Hess, W. W.; Frank, F. J. Tetrahedron Lett. 1968, 3363)], tetrapropylammonium perruthenate (Griffith, W. P.; Ley, S. V.; Whitcombe, G. P.; White, A. D. Chem. Commun. 1987, 1625; Griffith, W. F '. Aldrichimica Acta. 1990, 25, 13), and the like. The oxidation may be carried out in a solvent which does not adversely affect the reaction (e.g. acetone, dichloromethane, tetrahydrofuran, pyridine, NN-dimethylformamide, etc. or a mixture thereof). The reaction may be conducted above, at, or below ambient temperature.
In process (v), suitable alkylating reagents include, but are not limited to aldehydes and ketones in the presence of reducing agents (Hrubowchak, D. M.; Smith, F. X. Tetrahedron Lett. 1983, 24, 4951), alkyl-, aryl, or arylalkyl haUdes (Shono, T.; Kashimura, S.; Sawamura, M.; Soejima, T. J. Org. Chem. 1988, 53, 907). In the case that the reaction is conducted in the presence of an organic or inorganic bases such as an alkaUne earth metal (e.g. calcium, balium, magnesium, thallium etc.), an alkali metal hydride (e.g. sodium hydride, lithium hydride, etc.), an alkali metal hydroxide (e.g. sodium hydroxide, potassium hydroxide, etc.), an alkali metal carbonate (e.g. sodium carbonate, potassium carbonate, etc.), an alkali metal hydrogen carbonate (e.g. sodium hydrogen carbonate, potassium hydrogen carbonate, etc.), an alkali metal alkoxide (e.g. sodium methoxide, sodium ethoxide, thalUum ethoxide, potassium tert-butoxide, etc.), an alkali metal alkanoic acid (e.g. sodium acetate, etc.), a trialkylamine (e.g. triethylamine, trimethylamine, etc.), or a pyridine compound (e.g. pyridine, lutidine, picoUne, 4-N^V-dimethylaminopyridine, etc.), quinoUne, and the like. The alkylation may be carried out in a solvent which does not adversely affect the reaction (e.g. acetone, dichloromethane, tetrahydrofuran, pyridine, NN-dimethylformamide, etc. or a mixture thereof). The reaction may be conducted above, at, or below ambient temperature.
In process (w), suitable halogenation reagents include, but are not limited to halogens treated by iπadiation (sun lamp) for several hours (Heffher, R.; Safaryn, J. E.; Joullie, M. M.; Tetrahedron Lett. 1987, 28, 6539) or oxalyl chloride (Evans, D. A.; Dow, R. L.; Shih, T. L.; Takecs, J. M.; Zahler, R. J. Am. Chem. Soc. 1990, 772, 5290). The halogenation may be caπied out in a solvent which does not adversely affect the reaction (e.g. acetone, dichloromethane, tetrahydrofuran, pyridine, NN-dimethylformamide, etc. or a mixture thereof). The reaction may be conducted above, at, or below ambient temperature.
In process (x), suitable oxidation reagents include, but are not limited to oxodiperoxymolybdenum yridine)- 1 ,3-dimethyl-3,4,5,6-tetrahydro-2( lH)-pyrimidinone (Anderson, J. C; Smith, S. C. S1W E7T 1990, 2, 107) and oxodiperoxymolybdenum(pyridine)-hexamethylphosphoramide (Vedejs, E. J. Am. Chem. Soc. 1974, 96, 5944; Vedejs, E.; Engler, D. A.; Telschow, J. E. J. Org. Chem. 1978, 43, 188). The oxidation may be carried out in a solvent which does not adversely affect the reaction (e.g. acetone, dichloromethane, tetrahydrofuran, pyridine, NN-dimethylformamide, etc., or a mixture thereof). The reaction may be conducted above, at, or below ambient temperature.
In process (aa), suitable olefination reagents include, but are not Umited to Wittig reagents (Maecker, M., Org. React. 1965, 14, 270; Johnson, A. W., " Ylid Chemistry," Academic Press, New York, 1966) and CH2I2-Zn-TiCl4 [or Ti(NEt2)4] reagent (Hibino, J.; Okazoe, T.; Takai, K.; Nozaki, H. Tetrahedron Lett. 1985, 26, 5579; Okazoe, T.; Hibino, J.; Takai, K.; Nozaki, H. ibid. 1985, 26, 5581). The carbonyl olefination may be carried out in a solvent which. does not adversely affect the reaction (e.g. acetone, dichloromethane, tetrahydrofuran, pyridine, NN-dimethylformamide, etc., or a mixture thereof). The reaction may be conducted at room temperature.
In process (bb), suitable O-acylation reagents include, but are not Umited to alkyl, aryl, or arylalkyl acyl halides (Lakhvich, F. A.; Khlebnicova, T. S.; Akhrem, A. A. Synthesis 1985, 8, 784). The O-acylation may be carried out in a solvent which does not adversely affect the reaction (e.g. acetone, dichloromethane, tetrahydrofuran, pyridine, NN- dimethylformamide, etc., or a mixture thereof). The reaction may be conducted above, at, or below ambient temperature.
In process (cc), suitable amination reagents include, but are not Umited to amino acid derivatives and lower alkyl, aryl, or arylalkyl amines (Winkler, J. D.; Hershberger, P. M.; Springer, J. P. Tetrahedron Lett. 1986, 27, 5177). The reaction may be carried out in refluxing in benzene, toluene or a solvent which does not adversely affect the reaction (e.g. tetrahydrofuran, pyridine, NN-dimethylformamide, etc., or a mixture thereof). The reaction may be conducted at room temperature.
In process (dd), the alkyUdene formation may be caπied out using, but is not Umited to aldehydes and ketones with active methylene compounds. (Schonberg, A.; Singer, E. Chem. Ber. 1970, 103, 3871; Chatterjee, S. . Chem. Soc. B, 1969, 725). The alkyUdene formation may be carried out in a solvent which does not adversely affect the reaction (eg. acetone, dichloromethane, tetrahydrofuran, pyridine, NN-dimethylformamide, etc., or a mixture thereof). The reaction may be conducted under cooling to heating.
In process (ee), L may be hydroxy, or a good leaving group (halogen, tosylate, mesylate or ttiflate, for example). When a precursor compound contains a C(OH)-CH -C=O group, the elimination of H2O may be carried out in a solvent which is inert under the reaction conditions (e.g. toluene) with a trace of acid (e.g. toluenesulfonic acid), at a temperature selected from 50 to 100 °C. When the precursor compound contains a good leaving group, the elimination may be carried out in the presence of a base (e.g. triethyl amine or potassium carbonate), at a temperature selected from 0 to 100 °C.
In process (ff). suitable diamines include phenylene diamine and substituted 1,2- phenyl diamines, 2,3-diaminopyridine, 3,4-diaminopyridine, 4,5-diaminopyridazine, 4,5- diaminopyrimidine and their acid salts, preferably in the presence of tertiary amines (e.g. N- methylmorpholine). Suitable solvents include methanol, ethanol, propanol, acetonitrile, 2- butanone and NN-dimethylformamide, and a reaction temperature selected from 50 to 100 °C.
In process (gg), suitable reagents include sodium borohydride, zinc in acetic acid, sodium triacetoxyborohydride in acetic acid, lithium trialkoxyaluminum hydride in tetrahydrofuran, potassium or lithium tri-_.ec-butylborohydride in tetrahydrofuran, and borane/t-butylamine complex in a solvent such as methanol or ethanol. The reduction may be conducted at -70 °C to room temperature.
In process (hh), suitable 2-aminothiophenols include substituted 1,2- aminothiophenols, preferably in the presence of tertiary amine (e.g. N-methylmorpholine). Suitable solvents include methanol, ethanol and n-propanol; and the reaction may be conducted at a temperature selected from 50 to 100 °C.
In process (ii), the reagent to be used in this reaction may include di(lower)alkyl sulfoxide (e.g. dimethyl sulfoxide, ethyl methyl sulfoxide, propyl methyl sulfoxide, isobutyl methyl sulfoxide, butyl methyl sulfoxide, isobutyl methyl sulfoxide, hexyl methyl sulfoxide, etc). This reaction is usually conducted in the presence of oxalyl chloride, acid chlorides, lower alkanoic anhydride such as acetic anhydride in a conventional solvent that does not adversely influence the reaction such as dichloromethane, acetone, ethyl acetate, tetrahydrofuran, pyridine, N^V-dimethylformamide, etc., followed by the addition of a tertiary amine (e.g. triethyl amine). The reaction may be conducted at -70 °C to room temperature.
In process (jj), the dithiols are lower alkyl dithiols (e.g. ethanedithiol, propanedithiol or butanedithiol) and 1,2-aryl dithiols (e.g. 1,2-benzenedithiol) in the presence of a Lewis acid (e.g. boron trifluoride etherate or lanthanum trichloride) in a conventional solvent that does not adversely influence the reaction such as dichloromethane, tettahydrofuran or ether. The reaction may be conducted at -70 °C and room temperature.
In process (kk), suitable oxygen-substituted amines include hydroxyl amine, O- alkylhydroxyl amines, and O-arylalkyl hydroxyl amines, for example O-benzyl hydroxyl amine. Suitable solvents include those that do not adversely affect the reaction, for example ethanol or methanol. The reaction is preferably carried out with one equivalent of hydroxyl amine, and at a temperature of 25 to 100 °C, more preferably at the reflux temperature of the solvent.
In process (U), suitable hydrazines include alkylhydrazines (e.g. butylhydrazine), arylhydrazines (e.g. phenylhydrazine), acylhydrazines (e.g. acetylhydrazine), semicarbazides (e.g. t-butyloxycarbonyl hydrazine) and sulfonyl hydrazines (e.g. tosyl hydrazine) in a conventional solvent that does not adversely affect the reaction such as tettahydrofuran, methanol or ethanol. The reaction may be conducted at 20 to 100 °C.
In process (mm), 2-substitutions on the pyrimidine may be hydrogen, alkyl, aryl, hydroxyl, alkoxy, thiol, amino, alkylamino, arylamino, acylamino, carbamylamino, and sulphonylamino groups. The appropriate pyrimidine containing compounds may be prepared according to the methods described in " The Chemistry of Heterocyclic Compounds, Vol.16, supplement II, Chapter E, pp 21-60", D. J. Brown, John Wiley & Sons, 1985.
In process (nn), the furan containing compounds may be prepared according to the method described by Paulissen, R., et. al. in Tetrahedron Lett. 1974, 607. In process (oo), one equivalent of hydroxyl amine hydrochloride and tertiary amine (e.g. N-methylmorphoUne) in a conventional solvent that does not adversely affect the reaction such as tetrahydrofuran, methanol, ethanol or isopropanol is used to prepare the compound. The reaction is conducted at 20 to 100 °C.
In process (pp), the pyridine containing compounds may be prepared according to the literature: Osman, A. Ν.; Ismail, M. M.; Barakat, M. A. Rev. Roum. Chim. 1986, 31, 615- 624; Ried W.; Meyer, A., Ber. Deutsch. Chem. Ges. 1957, 90, 2841; Troschutz, R.; Troschultz, J.; SoUhuberkretzer, M. Arch Pharm. 1985, 318, 777-781.
In process (qq), a substituted 2-aminothiophenol, a 2-aminophenol or an aromatic 1,2- diamine is used in a conventional solvent that does not adversely affect the reaction such as tetrahydrofuran, ethanol, isopropanol, acetonitrile or NN-dimethylformamide. The reaction may be conducted at 20 to 100 °C.
In process (π), the keto-substituted furan containing compound may be prepared according to the literature: WilUams, P. H. et al, /. Am. Chem. Soc. 1960, 82, 4883; E. J. Corey et al., Chem. Lett. 1987, 223.
In process (ss), suitable l-halo-2-nitroaromatics may be substituted l-fluoro-2- nitrobenzene, o-fluoro-nitropyridines, or o-bromo-nitto-naphthalene, etc. The arylation may be carried out in a solvent which does not adversely affect the reaction (e.g. tettahydrofuran, NN-dimethylformamide, dimethoxyethane, diglyme, etc.).
The base used to generate the anion may be isopropyl magnesium chloride, lithium diisopropyl amine or sodium hydride. The reaction may be conducted at a temperature selected from -70 °C to 100 °C.
In process (uu), a nittile oxide may be formed either by oxidation of an aldoxime or dehydration of a nitro compound as described in the following references or literature cited therein: (1) Torssell, K. G. B. "Νittile Oxides, Νitrones and Νittonates in Organic Synthesis"; VCH Publishers: New York, 1988, p 64; (2) Kim, J. N.; Ryu, E. K. Synthetic Communications 1990, 20, 1373; (3) Chow, Y. L.; Shy, Y. Y.; Bakker, B. H.; PUlay, K. S. Heterocycles 1989, 29, 2245. The nittile oxide is placed in the presence of an alpha,beta- unsaturated enone in an inert solvent to yield an 2-isoxazoUnes. Any isomers may subsequently be chomatographically separated.
In process (zz), an isoxazoUne may be transformed to the coπesponding beta-hydroxy ketone using but is not limited to molybenum hexacarbonyl in wet acetonitrile according to: Baraldi, P. G.; Barco, A.; Benetti, S.; Manfredini, S.; Simoni, D. Synthesis 1987, 276. Alternatively, Ti3+ may be employed to attain N-O bond cleavage: Das, N. B.; Torssell, K. B. G. Tetrahedron 1983, 39, 2227. Additionally, Raney-nickel may also selectively cleave the N-O bond without reducing the imino functionality as described in the following reference and literature cited therein: Torssell, K. G. B. "Nittile Oxides, Nittones and Nittonates in Organic Synthesis"; VCH Publishers: New York, 1988, p 16 and 290. During the course of this transformation, a significant amount of dehydration occurs to produce alpha-beta unsaturated enones which may be separated from the beta-hydroxy ketones.
In process (eee), an aryl- or alkylsulfonyl hydrazone may be formed by treatment of a ketone with an aryl- or alkylsulfonyl hydrazide in the presence of an acid catalyst in a solvent suitable for the reaction such as methanol or ethanol at temperatures ranging from ambient to the reflux temperature of the solvent.
In process (hhh), an allyUc alcohol may be produced by selective reduction of an alpha-beta unsaturated enone. This is accomplished with but not Umited to sodium borohydride in the presence of cerium(IE) chloride heptahydrate in a suitable solvent such as methanol at or near 0 "C.
In process (iii), an epoxide may be produced on the central carbonyl of a tricarbonyl moiety by but not Umited to excess diazomethane as described in: Fisher, M. J.; Chow, K.; Villalobos, A.; Danishefsky, S. J. /. Org. Chem. 1991, 56, 2900-2907.
In process (jjj). Uberation of the ester to the acid may be achieved by the cleavage of a suitably substituted ester function. Such a functional group may be benzyl, 2,2,2- trichloroethyl, 9-fluorenylmethyl and the like. These are cleaved by methods well known to those skilled in the art.
In process (kkk), condensation of an amine with the acid may be performed using the mixed or symmetrical anhydride of said acid, or an ester of the acid, preferably activated, such as the ester derived from hydroxybenzotriazole, or the coπesponding acylcyanide, acylimidazole, or acylazide of the aforementioned acid.
In process (111), selective protection of the 32-hydroxyl moiety may be achieved using one of a variety of trialkylsilyl groups. This then leaves exposed a lone secondary alcohol on C-24 for selective inversion, which may be accomplished by activation of the 24-hydroxy as a mesylate, tosylate, etc., followed by inversion with a suitable nucleophile such as water, benzoic acid, formic acid, etc. On the other hand inversion of the unactivated 24-hydroxy group may be achieved using well described Mitsunobu conditions. Liberation of the silyl ether and inverted C-24 acylated hydroxy (if carboxylic acids are used as the nucleophile) is accomplished using methods weU known to those skilled in the art Alternatively, inversion may be accomplished without protection of the 32-hydroxyl group if ascomycin, FK506, or similar compounds are tteated with diethylaminosulfur trifluoride (DAST) in an inert solvent such as methylene chloride.
In process (mmm), condensation of an alkyloxy or substituted alklyoxy carbonyl hydrazine with ascomycin, FK506, similar compounds, or a suitable derivative thereof wherein the C-22 is available as a reactive center, including but not Umited to a carbonyl, is performed in an inert solvent such as methanol, ethanol, 2-propanol, etc., in the presence of a catalyst which may be an acid such as formic acid, p-toluenesulfonic acid, or camphor sulfonic acid. In process (ppp), L may be a hydroxyl group, or a good leaving group (halogen, tosylate, nittobenzenesulfonate, mesylate or ttiflate, for example).
The condensation may be caπied out in a solvent which does not adversely affect the reaction (e.g. isopropanol, acetonitrile, dioxane, NN-dimethylformamide, tettahydrofuran, etc.). The reaction may be caπied out in the presence of base (e.g. triethylamine, 4- methylmorphoUne or magnesium carbonate, etc.), at a temperature selected from 0 to 100 °C. The appropriate thiazole containing compound may be prepared according to Hantzsch's synthesis described by: Katritzky, A.R.; Rees, C.W. "Comprehensive Heterocyclic Chemistry"; Pergamon Press: Oxford, 1984, Vol. 6, Part 4B, p.294-299.
In process (qqq), L may be a hydroxyl group, or a good leaving group (halogen, tosylate, nittobenzenesulfonate, mesylate or ttiflate, for example).
The condensation may be caπied out in a solvent which does not adversely affect the reaction (e.g. isopropanol, t-butanol, acetonitrile, dioxane, NN-dimethylformamide, tettahydrofuran, etc.). The reaction may be caπied out in the presence of base (e.g. triethylamine, 4-methylmorpholine, potassium carbonate or magnesium carbonate, etc.), at a temperature selected from 0 to 100 °C.
Suitable amidines include formamidine, alkylamidines, arylamidines and alkylisoureas. Suitable guanidines include N-arylguanidines, N-acylated guanidines and N- sulfonylated guanidines.
In process (rπ), L may be a hydroxyl group, or a good leaving group (halogen, tosylate, nittobenzenesulfonate, mesylate or ttiflate, for example).
The condensation may be carried out in a solvent which does not adversely affect the reaction (e.g. isopropanol, t-butanol, acetonitrile, dioxane, NN-dimethylformamide, tettahydrofuran, etc.). The reaction may be carried out in the presence of a base (e.g., triethylamine, 4-methylmorphotine, potassium carbonate or magnesium carbonate), at a temperature selected from 0 to 100 °C.
The amides are primary amides such as formamide, alkylacylamides and arylacylamides.
In process (sss), the organometalUc reagent may be a Grignard reagent, an alkyllithium, or an aryllithium reagents.
The selective addition may be caπied out in a solvent which does not adversely affect the reaction (e.g., hexanes, ether, tettahydrofuran, dimethoxyethane or 2-methoxyethyl ether). The reaction may be caπied out in the presence of cerium (IE) at a temperature selected from -100 °C to O °C.
In process (ttt), the gamma amino alpha hydroxy carbonyl or a masked gamma amino alpha hydroxy carbonyl of a coπesponding compound prepared by process (sss) may have substitutions (e.g. alkyl, aryl groups, etc.) at the alpha and/or beta positions. Furthermore, the amino group may have N-alkyl or aryl substitutions. The condensation may be carried out in a solvent which does not adversely affect the reaction (e.g. isopropanol, t-butanol, acetonitrile, dioxane, N,N-dimethylformamide, tetrahydrofuran, etc.). The reaction may be caπied out in the presence of a base (e.g. triethylamine, 4-methylmorpholine, potassium carbonate or magnesium carbonate, etc.), at a temperature selected from 0 to 100 °C.
In process (uuu), the reaction is generally carried out in two steps: first the condensation of an alpha diketone or a masked alpha diketone with an l,2-diaminoalk__ne gives a dihydropyrazine. Once the dihydropyrazine has been prepared, it may be oxidized by air in the presence of Pd/C, PtO2 or other catalysts. Metal oxides (e.g. Mnθ2 or CuO) may also be used for the aromatization.
The condensation and oxidation may be carried out in a solvent which does not adversely affect the reactions (e.g. isopropanol, acetonitrile, dioxane, benzene, toluene, etc.). The reaction may be carried out in the presence of drying agent such as magnesium sulfate or molecular sieves at a temperature selected from 0 °C to 100 °C.
In process (wv), a 1,5-dicarbonyl group or a masked 1,5-dicarbonyl group prepared by process (sss) may have substitutions (e.g. alkyl, aryl groups etc.) at the alpha and/or beta positions. The condensation may be carried out with anhydrous ammonia in a solvent which does not adversely affect the reactions (e.g. Uquid ammonia, isopropanol, acetonitrile, dioxane, benzene, toluene, etc.). The reaction may be carried out at a temperature selected from -40 °C to 100 °C.
In process (www), a 1,4-dicarbonyl group or a masked 1,4-dicarbonyl group prepared by process (sss) may have substitutions (e.g. alkyl, aryl groups, etc.) at the alpha position.
The condensation and oxidation may be caπied out with anhydrous hydrazine in a solvent which does not adversely affect the reactions (e.g. isopropanol, acetonitrile, dioxane, benzene, toluene, etc.). The reaction may be carried out in the presence of a drying agent such as magnesium sulfate or molecular sieves at a temperature selected from 0 °C to 100 °C.
In process (xxx), the thiocarbonate formation may be carried out in a solvent which does not adversely affect the reactions (e.g. toluene, acetone, methylene chloride, tetrahydrofuran or pyridine, etc.). The reaction may be carried out in the presence of a base such as triethylamine, pyridine, dimethylaminopyridine and sodium carbonate at a temperature selected from 0 °C to 100 °C. The thiocarbonylating reagent may be N,N'-thiocarbonyl-diimidazole, N,N-thiocarbonylbis(2-pyridone), thiophosgene, or O-phenylthiochloroformate.
In process (yyy), the carbonate formation may be carried out in a solvent which does not adversely affect the reactions (e.g. toluene, acetone, butanone, methylene chloride, tettahydrofuran or pyridine etc.). The reaction may be carried out in the presence of a base such as triethylamine, pyridine, dimethylaminopyridine and sodium carbonate at a temperature selected from 0 °C to 100 °C. The carbonylating reagent may be N,N'-carbonyldiimidazole, N,N'-carbonyl-b Iy- (2-pyridone), phosgene, triphosgene, ethyl chloroformate, ethyl trichloroacetate, or o- phenylchloroformate.
In process (zzz), the cyclic phosphonate formation may be caπied out by first reacting a diol from a selected compound with phosphorous trichloride followed by the addition of an appropriate alcohol and amine. The alcohol used may be an alkyl alcohol, or an aryl alcohol. The amine used may be primary or secondary. Alternatively, the cyclic phosphonate formation may be caπied out by directly reacting the diol from a coπesponding compound with an appropriate alkoxyphophoryl dichloride.
The phosphonate formation may be carried out in a solvent which does not adversely affect the reactions (e.g. carbon tettachloride, chloroform, methylene chloride, toluene, tetrahydrofuran, etc.). The reaction may be carried out in the presence of a base such as triethylamine, pyridine, dimethylaminopyridine, and sodium carbonate at a temperature selected from 0 °C to 100 °C.
In process (aaaa), the reduction of thiocarbonate may be carried out in a solvent which does not adversely affect the reactions (e.g., toluene or tettahydrofuran) at a temperature selected from 0 °C to 100 °C.
The reducing agent used may be trimethylphosphite, triethylphosphite, trialkylphosphite or tti-n-butyltin hydride.
In process (bbbb), the reduction of a 1,2-dicarbonyl group of a coπesponding compound may be caπied out in a solvent which does not adversely affect the reactions (e.g., methanol, ethanol, ethanol, pyridine or N,N-dimethylformamide).
The reducing agents used may be tin amalgam, aluminum amalgam with hydrogen chloride in ethanol, or may be hydrogen sulfide in pyridine or N,N-dimethylformamide.
In process (cccc), the reduction and condensation of a 2-(o-nitrophenyl)-l,3-diketone of a coπesponding compound may be carried in a solvent which does not adversely affect the reactions (e.g. ethanol, tettahydrofuran, ethyl acetate or benzene, etc.).
The reducing agents used may be hydrogen gas over Pd/C, or Pt/C, zinc dust with ammonium chloride, zinc dust with hydrochloric acid at a temperature selected from 0 °C to 100 °C.
In process (dddd), triazole formation may be caπied out using, but is not Umited to an azide derivative with suitable acetylene analogues include diethylacetylene dicarboxylate, dimethylacetylene dicarboxylate, methyl cyanoacetylenecarboxylate, and the likes. The reaction may be conducted above, or below ambient temperature, more preferably from 0 to 50 °C.
In process (eeee), pyπole formation may be carried out using, but is not limited to amine compounds with 1,4-dicarbonyl analogues, such as acetonylacetone, and the likes. Suitable solvents include methanol, ethanol, n-propanol, isopropanol, acetonitrile and N,N-dimethylformamide. The reaction may be conducted above, or below ambient temperature, more preferably from 50 to 100 °C.
In process (ffff), suitable reagents for vicinal hydroxylation include osmium tettaoxide, potassium permanganate, and iodine in conjunction with silver acetate. Osmium tettoxide is preferably used with a regenerating agent such as hydrogen peroxide, alkaline t- butyl hydroperoxide or N-methylmorphoUne-N-oxide, and a solvent that does not adversely affect the reaction, for example diethyl ether or tettahydrofuran. Potassium permanganate is preferably used in mild conditions, for example alkaUne aqueous solution or suspensions. Co-solvents such as t-butanol or acetic acid may also be used. Iodine-silver acetate under 'wet' conditions yields ci-diols. Preferably, iodine is used in aqueous acetic acid in the presence of silver acetate. Iodine-silver acetate under 'dry' conditions yields trans-diols. Here, the initial reaction is carried out in the absence of water, and final hydrolysis yields the diol. In each case, the oxidation is preferably caπied out at a temperature of 0 to 100 °C.
Suitable reagents for the oxidative cleavage of the vicinal diol include lead tetraacetate, phenyliodoso acetate, periodic acid or sodium metaperiodate. Suitable solvents for the first two reagents include benzene and glacial acetic acid. The second two reagents are preferably used in aqueous solution. The reaction is preferably carried out at a temperature of 0 to 100 °C.
In process (gggg), suitable reagents for the oxidation of an aldehyde of the coπesponding compound may include silver oxide, chromic acid and potassium permanganate. In the presence of a variety of catalysts, oxygen may also be used in converting an aldehyde to a carboxylic acid of a coπesponding compound. The catalysts may be palladium or platinum oxide. The air oxidation may be caπied out in a solvent which does not adversely affect the reaction (e.g., ethanol, water, acetonitrile, aqueous acetone or pyridine) at a temperature of 0 to 100 °C.
In process (hhhh), esters of a coπesponding carboxylic acid may be prepared under neuttal conditions at room temperature by the reaction of the carboxyUc acid with alcohols in the presence of molar amounts of activating reagents such as triphenyl phosphine and diethyl azodicarboxylate, carbodnmides, N,N'-carbonyldiimidazole and l-methyl-2-halopyridinium iodide. Esters may also be formed by reacting the coπesponding carboxylic acid with diazoalkanes in a solvent which does not adversely affect the reaciton (e.g., ether, tetrahydrofuran or methylene chloride) at a temperature of from 0 to 100 °C.
In process (uii), the cyclopropanation of the allyl group of a coπesponding compound may be caπied out with diazoalkanes in a solvent which does not adversely affect the reaction (e.g., ether, methylene chloride or tettahydrofuran) in the presence of a catalyst such as palladium (II) acetate. The temperature of the reaction is of -15 to 5 °C.
In process (jjjj), a pyπόle ring may be produced by reacting a 1,4-dicarbonyl group of a coπesponding compound with ammonia, or a substituted amine such as benzylamine or 2- aminoethanol. Suitable solvents include those which do not adversely affect the reaction (e.g., methylene chloride, tetrahydrofuran or dioxane). The reaction is preferably caπied out at a temperature of 0 to 100 °C.
In process (kkkk), the cyclization of a 1,4-dicarbonyl group of a coπesponding compound may be carried out in the presence of a catalytic amount of acid (e.g., acetic acid or arylsulfonic acid). The reaction may be caπied out in a solvent which does not adversely affect the reaction (e.g., methylene chloride, ether, benzene or toluene). The reaction is preferably carried out at a temperature of 0 to 60 °C.
In process (1111), suitable reagents include air, a palladium (E) haUde (e.g. palladium (E) chloride), in conjunction with a cuprous halide (e.g. cupper (I) chloride). Suitable solvents include those that do not adversely affect the reaction (e.g. DMF and water). The reaction is preferably caπied out at a temperature of 0 to 100 °C.
In process (nnnn), suitable reducing agents include but are not limited to sodium cyanoborohydride, lithium aluminum hydride, borane-pyridine, or hydrogen in the presence of such catalysts as Raney nickel, platinum, platinum oxide, or palladium. An acidic environment may promote the reduction in some cases, and acids such as hydrochloric acid or p-toluenesulfonic acid may be added for this purpose. The reduction may be caπied out in a solvent which does not adversely affect the reaction (e.g. ethanol, ethyl acetate).
In process (oooo), reduction of an oxime to the coπesponding amine may be accomplished with but not Umited to hydrogenation with a suitable catalyst such as palladium on carbon in a solvent inert to the reaction conditions (e.g. ethanol) at temperatures ranging from 0 to 100 °C.
In process (pppp), reduction of an enone to the coπesponding saturated ketone may be accomplished with but not limited to hydrogenation with a suitable catalyst such as either palladium on carbon or rhodium on alumina in a solvent inert to the reaction conditions (e.g. methanol, ethanol, isopropanol, ethyl acetate) in a temperature range from -78 to 100 °C.
In process (qqqq), isoxazoline formation may be accompUshed by, but not Umited to the following sets of reaction conditions involving a beta-hydroxy oxime. One possible method is to treat the beta-hydroxy oxime with Martin's sulfurane dehydrating reagent at or near room temperature in a solvent inert to the reaction conditions such as methylene chloride. Alternatively, the beta-hydroxy oxime may be tteated with p-toluenesulfonyl chloride in a solvent such as pyridine at temperatures ranging from 0 to 100 °C.
In process (rπr), an intramolecular aldol reaction may be accomplished by, but is not limited to treatment of a carbonyl with a base such as potassium or sodium hydride in a solvent which is inert to the reaction conditions (e.g. tettahydrofuran or N,N- dimethylformamide) at a temperature range from -78 to 150 °C.
In process (ssss), a cyclic imine may be formed by, but is not Umited to treatment of an alpha,beta-unsaturated enone with the sodium enolate of a glycine ester imine in an inert solvent such as tetrahydrofuran in a temperature range from -78 to 100 "C. Upon aqueous workup, the imine hydrolyzes and spontaneously cyclizes to form the cycUc imine.
In process (tttt), a substituted pyπole may be formed by but is not Umited to a 1,3-dipolar cycloaddition between an alpha,beta-unsaturated enone with a glycine ester imine in the presence of a suitable catalyst such as lithium bromide and triethylamine in a solvent inert to the reaction conditions (e.g. tettahydrofuran) at or near room temperature.
In process (uuuu), alpha diazoketones can be decomposed by exposure to UV light or by heating. Wolff reaπangements often ensue yielding beta-keto carboxylic acids when run in a solvent mixture containing water, beta-keto esters when run in a solvent containing an alcohol, or beta-keto amides when run in a solvent containing ammonia, a primary or a secondary amine.
Moreover, in process (wvv), if a beta-keto carboxylic acid is formed, decarboxylation can occur spontaneously or by heating.
In process (yyyy), aryl-, heterocyclic-, or alkyloxycarbonylation may be caπied out using aryl-, heterocycUc-, or alkyl- chloroformate in the presence of amines like triethylamine, dUsopropylethylamine, pyridine and the like. Alternatively, the reaction may be carried out by reacting the coπesponding aryl-OH, heterocycUc-OH or alkyl-OH with -CHOC(O)Cl or -CHOC(O)-(p-nittophenyl) in a coπesponding compound in the presence of amine base. The reaction may be carried out in a solvent which does not adversely affect the reaction (e.g. acetone, dichloromethane, tetrahydrofuran, pyridine and N,N- dimethylformamide, or a mixture thereof). The reaction may be conducted above, at or below ambient temperature.
In process (zzzz) allylic oxidations may be caπied out using selenium dioxide with or without a co-oxidant, such as tert-butyl hydroperoxide, in an inert solvent such as tettahydrofuran, ether, ethylacetate, water, or a combination thereof. The reaction may be conducted at room temperature to 100 °C.
The compounds of the present invention are formed by modification of FR-900520 (ascomycin) or one of its congeners (such as FK-506, etc.) by alkylation of the C-32- hydroxyl group with optional modifications exercised at C-18 and/or C-21 and/or C-23 and/or C-24. The compounds, processes and uses of the present invention will be better understood in connection with the following examples, which are intended as an illustration of and certainly not a limitation upon the scope of the invention. Both below and throughout the specification, it is intended that citations to the literature are expressly incorporated by reference. - CHoC OCoHs (R-Configurationl.
A solution of ascomycin (0.5 g, 0.63 mmol) in dichloromethane (10 mL) containing rhodium(E)acetate dimer (3 mg) was refluxed while ethyl diazoacetate (66 uL, 0.63 mmol) in dichloromethane (1 mL) was added dropwise. After complete addition the reaction was refluxed for 30 minutes and additional ethyl diazoacetate (132 uL, 1.26 mmol) in dichloromethane (1.5 mL) was added dropwise with reflux continuing 30 minutes after complete addition. Solvent was removed in vacuo and the residue purified by HPLC on silica gel eluting with hexane:acetone (3:1). Fractions containing desired product were pooled, concentrated, dissolved in CCI4, and concentrated to constant weight under high vacuum to give the desired product (274 mg) as an oil in 50% yield. IR (CDCI3) 3500, 2930, 1742, 1700, 1645, 1452 cm'1; 13C NMR (125 MHz) delta 9.4, 11.7, 14.1, 14.2, 15.8, 16.2, 20.5,
21.1, 24.2, 24.6, 26.3, 27.6, 30.3, 30.8, 32.7, 32.9, 33.6, 34.6, 36.4, 39.2, 39.7, 43.1, 48.7, 54.7, 56.3, 56.6, 56.9, 57.2, 60.6, 68.5, 70.1, 72.9, 73.7, 75.2, 77.2, 82.8, 83.6, 97.0, 123.1, 129.6, 132.4, 138.7, 164.7, 169.0, 171.1, 196.1, 213.5; MS (FAB) m/z M+K = 916; Anal, calc'd. for C47H75NO14-1.0 CCI4. C, 54.70; H, 7.33; N, 1.36. Found: C, 54.42; H, 7.22; N, 1.26.
The prior procedure was modified using benzyl diazoacetate instead of ethyl diazoacetate.
Ascomycin (0.5 g) provided title compound (0.1 g) in 20% yield, mp. 65-72 °C; IR (CDCI3)
3510, 2930, 1740, 1695, 1642, 1450 cm'1; 13C NMR (125 MHz) delta 9.4, 11.7, 14.1, 15.8,
16.2, 20.4, 21.1, 24.1, 24.5, 26.3, 27.6, 30.3, 30.8, 32.7, 32.8, 34.4, 34.5, 36.3, 39.2, 39.6, 43.1, 48.6, 53.4, 54.6, 56.3, 56.6, 57.1, 66.3, 68.5, 70.1, 72.8, 73.6, 75.1, 76.8, 82.7, 83.6, 96.9, 123.0, 128.3, 128.4, 128.5, 129.5, 132.3, 135.6, 138.7, 164.7, 168.9, 171.0, 196.2, 213.4; MS (FAB) m/z: M+H-H2O = 922, M+K = 978. Anal, calc'd. for C52H77NO14: C, 66.43; H, 8.26; N, 1.49. Found: C, 66.12; H, 8.14; N, 1.41.
Example 3: Formula I: R= ethyl: n= 1: R2=R2a=R3=R5=H: R4=QH: Rla=QCHr. RJ= -OCHo O'.OH (R-Confi uration..
The resultant product of Example 2 (25 mg, 0.03 mmol) and 10% Pd/C (3 mg), were placed in a flask and the vessel was flushed with nitrogen for 10 min. Methanol (250 uL) was added via syringe, and the reaction stiπed under a hydrogen atmosphere (1 atm) for 45 min. The mixture was filtered, the catalyst washed with additional methanol (1 mL), and the solvent removed in vacuo. The resulting residue was partitioned between ethyl acetate (5 mL) and water (5 mL), the organic layer was dried (MgSO4), filtered and concentrated to constant weight, thus producing the title compound (23 mg) as a white powder. MS (FAB) mlz: M+K = 888.
The product of Example 3 (0.50 g, 0.59 mmol) was dissolved in dichloromethane (5 mL) and the solution cooled to 0°C. 4-Dimethylaminopyridine (DMAP) (14.4 mg, .0.118 mmol) was added foUowed by l-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (ED AC) (206 mg, 1.07 mmol) then benzylamine (128.3 uL, 1.18 mmol). The reaction was warmed to room temperature and stiπed overnight. Ethyl acetate (150 mL) was added and the organic phase washed with IN hydrochloric acid (HC1) (2 x 150 mL), saturated bicarbonate solution (2 x 150 mL), and then brine (2 x 150 mL). The organic layer was dried using anhydrous sodium sulfate(Na2SO4), filtered, and solvent removed in vacuo to give 395.7 mg yellow foam. The crude product was purified by HPLC (30 x 300 mm silica column) eluting with 2:1 hexane/acetone. Fractions containing product were combined and solvent removed in vacuo to give the title compound (273.2 mg, 49% yield) as a white soUd: MS (FAB) m/z: (M+K)=977.
Example 5: Formula I: R= ethyl: n= 1: R2=R2__=R3=R5=H: R4=OH: R L-^OCH R- The resultant product of Example 3 (0.8 g, 0.94 mmol) was dissolved in THF (3 mL) and the solution cooled to 0°C before adding N-methylmorpholine (103.4 uL, 0.94 mmol) followed by isobutyl chloroformate (122.2 uL, 0.94 mmol). The resulting suspension was stiπed for 20 minutes at 0 °C after which N-methylbenzylamine (243 uL, 1.88 mmol) was added. Stiπing was continued overnight as the ice melted. The reaction mixture was loaded onto sitica (40 mL) in a fritted funnel then eluted with dichloromethane (100 mL), 2:1 hexane/acetone (200 mL), 1:1 hexane/acetone (200 mL), and acetone (100 mL). Fractions containing product were combined and solvent removed in vacuo to give 0.64 g yellow foam. The crude product was further purified by HPLC (30 x 300 mm sUica column) eluting with 1.5:1 hexane/acetone to provide the title compound (523 mg, 58% yield) as a white foam. MS (FA )m/z: (M+K)=991.
Example 6: Formula I: R= ethyl: n= 1: R2=R a=R_i=R5=H: R4_=QH: RJ-^OCHg: Rl= -OCH9C(O.Rl2 (R-Configuration.: Rl2_= NRHRI≤; RI^RJL^ H
The crude isolate from Example 81 (1.5 g, ~1.2 mmol ) was dissolved in THF (4 mL) and the solution cooled to 0°C before adding N-methylmorpholine (129.4 uL, 1.2 mmol) followed by isobutyl chloroformate (152.8 uL, 0.59 mmol). The resulting suspension was stiπed for 20 minutes at 0°C after which ammonium hydroxide (14.8M, 159.2 uL, 2.4 mmol) was added. Stiπing was continued overnight as the ice melted. The reaction mixture was loaded onto silica (80 mL) in a fritted funnel then eluted with dichloromethane (200 mL), 2:1 hexane/acetone (400 mL), 1:1 hexane/acetone (400 mL), and acetone (200 mL). Fractions containing product were combined and solvent removed in vacuo to give 358 mg yellow foam. The crude product was further purified by RP-HPLC (Rainin Dynamax 41.4 mm phenyl column) eluting with a gradient of 20% methanol/water and acetonitrile to provide the title compound (188.7 mg, 19% yield) as a white foam. MS (FAB)w/z: (M+K)=887.
The product of Example 3 is activated as in Example 5 and then tteated with methylamine instead of N-methylbenzylamine to provide the title compound.
The product of Example 3 is activated as in Example 5 and then tteated with dimethylamine instead of N-methylbenzylamine to provide the title compound.
Example 9: Formula I: R= ethyl: n= 1: R2=R2a=R_i=R5=H: R =OH: Rla=OCHτ. Rl= -OCTbC.O.Rl2- (R-Configuration .: RJ2= NRHR15: R1A= H: RJ5= ethyl. The product of Example 3 is activated as in Example 5 and then tteated with ethylamine instead of N-methylbenzylamine to provide the title compound.
The product of Example 3 is activated as in Example 5 and then treated with N,N- methyl,ethylamine instead of N-methylbenzylamine to provide the title compound.
The product of Example 3 is activated as in Example 5 and then tteated with propylamine instead of N-methylbenzylamine to provide the title compound.
The product of Example 3 is activated as in Example 5 and then tteated with N,N-methyl,propylamine instead of N-methylbenzylamine to provide the title compound. The product of Example 3 is activated as in Example 5 and then treated with 2-aminopropane instead of N-methylbenzylamine to provide the title compound.
The product of Example 3 is activated as in Example 5 and then tteated with N,N-methyl, 2- propylamine instead of N-methylbenzylamine to provide the title compound.
The product of Example 3 is activated as in Example 5 and then tteated with cyclopropylamine instead of N-methylbenzylamine to provide the title compound.
The product of Example 3 is activated as in Example 5 and then treated with n-butylamine instead of N-methylbenzylamine to provide the title compound.
The product of Example 3 is activated as in Example 5 and then tteated with N,N-methylbutylamine instead of N-methylbenzylamine to provide the title compound.
Example 18: Formula I: R= ethyl: n= 1: R2=R2a=R =R5--:H: R4=QH: RI^OCH^: RI= -OCH C(Q)R±2 (R-Configuration .: Rl2 ^ NRMRI^: R!4= H: R±5= -CTbCH^H^. The product of Example 3 is activated as in Example 5 and then tteated with isobutylamine instead of N-methylbenzylamine to provide the title compound.
Example 19: Formula I: R= ethyl: n= 1: R-__-_R2a=R3=R5=H: R4=QH: RJ^OCH^: R^= -OCH2C(O l2 (R-Configuration : Rl2= NRI4R__5: R14= CH^: Rl^-C^CHfCH^. The product of Example 3 is activated as in Example 5 and then tteated with N,N-methyl,isobutylamine instead of N-methylbenzylamine to provide the title compound. The product of Example 3 is activated as in Example 5 and then tteated with cyclobutylamine instead of N-methylbenzylamine to provide the title compound.
-CHϊCHoCI CΗoCHq.
The product of Example 3 is activated as in Example 5 and then treated with pentylamine instead of N-methylbenzylamine to provide the title compound.
Example 22: Formula I: R= ethyl: n= 1: R2=R2a=R3_=R5=H: R4=OH: RI^OCH^: R^=
-0CH2C(0)RI2 (R-Configuration): Rl2= NRJ4RI5: R.14^ CHv. RJ5=
-CH2CH2CH2CU2CH3,
The product of Example 3 is activated as in Example 5 and then treated with
N,N-methyl,pentylamine instead of N-methylbenzylamine to provide the title compound.
The product of Example 3 is activated as in Example 5 and then tteated with 3-methylbutylamine instead of N-methylbenzylamine to provide the title compound.
Example 24: Formula I: R= ethyl: n= 1: R2=R2a=R2=R.5=H: R4=OH: RI^OCH^: Rl= -OCH2C(O)Rl2 (R-Configuration): Rl2= NRI4R_15: R!4= C : R1≤=
The product of Example 3 is activated as in Example 5 and then treated with N,N-methyl,3- methylbutylamine instead of N-methylbenzylamine to provide the title compound.
The product of Example 3 is activated as in Example 5 and then treated with cyclopentylamine instead of N-methylbenzylamine to provide the title compound.
Example 26: Formula I: R= ethyl: n= 1: R___--R2a=R3=R5=H: R4=QH: RJL-^QCH^: Rl=
-OCH2 R12 (R-Configuration): RJ2= RHR1 : R14= H: RJ^-
The product of Example 3 is activated as in Example 5 and then tteated with n-hexylamine instead of N-methylbenzylamine to provide the title compound. Example 27: Formula I: R= ethyl: n= 1: R___--R2a=R-=R5-=H: R4=OH: RI^OCH^: RL=
-0CH2C 0)RI2 (R-Configuration): Rl2= NRI4RI5: RJ4= CHV. R15=
The product of Example 3 is activated as in Example 5 and then tteated with
N,N-methyl,hexylamine instead of N-methylbenzylamine to provide the title compound.
The product of Example 3 was activated as in Example 5 and then tteated with cyclohexylamine instead of N-methylbenzylamine to provide the title compound. MS (FAB) m/z: M+H = 931.
-CH2CH2OCH2CH2-. thus forming a six membered ring incorporating the nittogen to which they are attached.
The product of Example 3 was activated as in Example 4 and then tteated with morpholine instead of benzylamine to give the title compound. MS ~~AB)m/z: (M+K)=957.
The product of Example 3 was activated as in Example 4 and then tteated with 2-aminoethanol instead of benzylamine to give the title compound. MS (FAB )m/z: (M+K)=931.
Example 31: Formula I: R= ethyl: n= 1: R_ R2a=R3__.R5=H: R =OH: RI^QCH^: RJ= -0CH2C 0)RI2 (R-Configuration): Rl2= NR14R15: R!4= H: R15_= -CH2CH2CH2OH. The product of Example 3 was activated as in Example 4 and then treated with 3-aminopropanol instead of benzylamine to give the title compound. MS (FAB)rn/z: (M+K)=945.
The product of Example 3 was activated as in Example 5 and then tteated with
4-aminobutanol instead of N-methylbenzylamine to give the title compound. MS (FAB)m/z:
(M+K)=959.
The product of Example 3 is activated as in Example 5 and then treated with
5-hydroxypentylamine instead of N-methylbenzylamine to provide the title compound.
The product of Example 3 is activated as in Example 5, and then tteated with 1,2-diaminoethane instead of N-methylbenzylamine to provide the title compound.
Example 35: Formula I: R= ethyl: n= 1: R_-_-.R2a=R =R-!=H: R4=OH: RI^QCH^: RJ= -OCH2C O)R12 (R-Configuration): RJ2= NRURIJ; R!4= H: RJ^ -CH2CH2CH2NH2- The product of Example 3 is activated as in Example 5, and then tteated with 1,3-diaminopropane instead of N-methylbenzylamine to provide the title compound.
Example 36: Formula I: R= ethyl: n= 1: R2=R2__=R_i=R5=H: R4=OH: RJ---=OCHτ. Rl=
-OCH2C(O)R12 (R-Configuration): Rl2= N 14R15: R!^ H: R!^
The product of Example 3 is activated as in Example 5, and then tteated with
1,4-diaminobutane instead of N-methylbenzylamine to provide the title compound.
The product of Example 3 is activated as in Example 5, and then tteated with
1,5-diaminopentane instead of N-methylbenzylamine to provide the title compound.
The product of Example 3 was activated as in Example 4 and then tteated with glycine benzyl ester instead of benzylamine to give the title compound. MS (FAB)/n/z: (M+K)=1035. Example 39: Formula T: R= ethyl: n= 1: R =R2a=R3=R5=H: R4=OH: Rli^OCH^: RJ= -0CH C(0)R12 (R-Configuration): RI2= NR RI : R!^ H: R! = -CT^CCbH.
The title compound was synthesized in the manner described in Example 3 substituting the product from Example 38 for the product from Example 2. MS (FAB)rø/z: (M+K)=945.
The product of Example 3 was activated as in Example 4 and then tteated with beta-alanine benzyl ester instead of benzylamine to give the title compound. MS (FAB) /z; (M+K)=1049.
The title compound was synthesized in the manner described in Example 3 substituting the product from Example 40 for the product from Example2. MS (FAB) /z: (M+K)=959.
configuration).
The product of Example 3 is activated as in Example 5, and then tteated with
(R)-2-aminopropanoic acid instead of N-methylbenzylamine to provide the title compound.
Example 43: Formula I: R= ethyl: n= 1: R-^R-^R^R-^H: R___=OH: RI^OCH^: Rl=
-0CH9C(0)R12 (R-Configuration): Rl2= NR1 R15: R!^ H: R!^ -CH CH )CO H (S configuration).
The product of Example 3 is activated as in Example 5, and then tteated with
(S)-2-aminopropanoic acid instead of N-methylbenzylamine to provide the title compound.
-CH(CH3)CONHCH(CH3)CONHCH(CH3)CO2H (all chiral centers in R-H are R configuration).
The product of Example 3 is activated as in Example 5, and then tteated with D-alaninyl-D- alaninyl-D-alanine instead of N-methylbenzylamine to provide the title compound. Example 45: Formula I: R= ethyl: n= 1 : R^ ^R^R^H: R4=OH: Rl^OCHr. ±= -0CH2C 0)R12 (R-Configuration): RJ2= NRJ4RI5: R = H: RJ_-J= 3-phenyl-phenyl. The product of Example 3 is activated as in Example 5 and then tteated with 3-biphenylamine instead of N-methylbenzylamine to give the title compound.
phenyl.
The product of Example 3 is activated as in Example 5 and then treated with N,N-(ethanol-2- yl)-(3-biphenyl)-amine instead of N-methylbenzylamine to give the title compound.
Example 47: Formula I: R= ethyl: n= 1: R- R-^R-^R^H: R4=OH: RI^OCH^: Rl=
-0CH2C(0)RI2 (R-Configuration): R-\2= N - RU; RII .
-CH2CH2N CH ). CH2CH2OH): R±5= phenyl.
The product of Example 3 is activated as in Example 5 and then treated with N-phenyl-
N'-methyl-N'-(ethanol-2-yl)-ethyldiamine instead of N-methylbenzylamine to give the title compound.
Example 48: Formula I: R= ethyl: n= 1: R2=R2___=R =R5=H: R4=OH: RJa=OCHr. Rl= phenyl.
The product of Example 3 is activated as in Example 5 and then treated with N-phenyl-N',N'- dimethyl-ethyldiamine instead of N-methylbenzylamine to give the title compound.
Example 49: Formula I: R= ethyl: n= 1: R2=R a=R3=R5=H: R4=OH: RI^OCH^: Rl=
-0CH2C(0)RI2 (R-Configuration): Rl = NR RI5: R!^ CH2(3-pyridv1): Rl5= CH9(3- pyridyl).
The product of Example 3 was activated as in Example 5 and then tteated with
3,3'-dipipicolylamine instead of N-methylbenzylamine to give the title compound. MS
(FAB) m/z: M+K = 1069.
Example 50: Formula I: R= ethyl: n= 1: R2=R2___=R3=R5=H: R4=OH: RIJ^QCH^: Rl= -0CH2C 0)R12 (R-Configuration): Rl2-= NRI4RI5: R-l cvclohexyl: R_ -= cvclohexyl. The product of Example 3 is activated as in Example 5 and then treated with dicyclohexylamine instead of N-methylbenzylamine to give the title compound.
Example 51: Formula I: R= ethyl: n= 1: R-^R-^R-^R- l: R-----OH: Rla=OCH^: RJ= -0CH2C(0)RI2 (R-Configuration): RJ2= NR14R15: RJ^, H: RJ5= NH-.4-morpr.nl .nylV The product of Example 3 was activated as in Example 5 and then treated with 1 equivalent of 4-aminomorpholine and 0.1 equivalents of 4-dimethylaminopyridine instead of N- methylbenzylamine to give the title compound. MS (FAB) m/z: M+K = 972.
The product of Example 3 was activated as in Example 5 and then tteated with thiomorpholine instead of N-methylbenzylamine to give the title compound. MS (FAB) m/z: M+K = 973.
Example 53: Formula I: R= ethyl: n= 1: R2=R2_-=R-__--R5=H: R4=OH: RJa^OCH^: Rl= -OCH2C O)RI2 (R-Configuration): R±2= NR14R15: RJ^ H: R15= 4-CFς-phenyl. The product of Example 3 was activated as in Example 4 and then tteated with 4-aminobenzotrifluoride instead of benzylamine to give the title compound. MS (FAB)m/z: (M+K)=1031.
Example 54: Formula I: R= ethyl: n= 1: R2=R2a=R___--R5=H: R =OH: Rla^OCHr. RJ= -0CH2C 0)RI2 (R-Configuration): Rl2= N MRJ ; R!X= H: Rl5= 4-F-phenyl. The product of Example 3 was activated as in Example 4 and then treated with 4-fluoroaniline instead of benzylamine to give the title compound. MS (FAB)m/∑: (M+K)=981.
phenyl.
The product of Example 3 was activated as in Example 4 and then tteated with
4-morpholinoaniline instead of benzylamine to give the title compound. MS (FAB)w/z:
(M+K)=1048.
The product of Example 3 was activated as in Example 5 and then tteated with p-aminophenol instead of N-methylbenzylamine to give the title compound. MS (FAB)m/z: (M+K)=979.
Example 57: Formula I: R= ethyl: n= 1: R2=R2a=R_i=R5=H: R4=OH: RJi^O H^; R- -OCH2C O)R12 (R-Configuration): Rl2= NR RI5; R1X= H: RH = 3-pyridyl. The product of Example 3 was activated as in Example 5 and then treated with 3-aminopyridine instead of N-methylbenzylamine to give the title compound. MS (FAB)m/z: (M+K)=964.
The product of Example 3 was activated as in Example 5 and then treated with 4-aminopyridine instead of N-methylbenzylamine to give the title compound. MS (FAB)m/z: (M+K)=964.
The product of Example 3 was activated as in Example 5 and then treated with 2-aminopyridine instead of N-methylbenzylamine to give the title compound. MS (FAB)m/z: (M+K)=964.
The product of Example 3 was activated as in Example 5 and then tteated with 2-(methylamino)ethanol instead of N-methylbenzylamine to give the title compound. MS (FAB)m/z: (M+K)=945.
The product of Example 3 is activated as in Example 5 and then tteated with methylcarbazate instead of N-methylbenzylamine to give the title compound.
Example 62: Formula I: R= ethyl: n= 1: R^R ^R^R^H: R =OH: Rla^OCH^: Rl= -0CH2C(0)R12 (R-Configuration): R-\---<- L-prolinocarboxamide. The product of Example 3 is activated as in Example 5 and then tteated with L-prolinecarboxamide instead of N-methylbenzylamine to give the title compound.
The product of Example 3 is activated as in Example 5 and then tteated with D-ProUnecarboxamide instead of N-methylbenzylamine to give the title compound. Example 64: Formula I: R= ethyl: n= 1 : R-^R-^R-^R- i: R4=OH: RJ^OCH^: R±-= -OCH9C(O)RJ (R-Configuration): RJ2= L-prolinol.
The product of Example 3 is activated as in Example 5 and then tteated with L-prolinol instead of N-methylbenzylamine to give the title compound.
The product of Example 3 is activated as in Example 5 and then treated with D-prolinol instead of N-methylbenzylamine to give the title compound.
The product of Example 3 is activated as in Example 5 and then tteated with N-(ethanol-
2-yl)-N'-carbomethoxy-hydrazine instead of N-methylbenzylamine to give the tide compound.
(phenylethynyl)phenyl.
The product of Example 3 is activated as in Example 5 and then tteated with
3-phenylethynylaniline instead of N-methylbenzylamine to give the title compound.
Example 68: Formula I: R= ethyl: n= 1: R-^R-^R- R^H: R4=OH: RI^OCH^: RJ=
-OCH2C(O)R12 (R-Configuration): R±2-= NR RI5-: R1 = CH2CH2CH OH: R_J5= 4- fluorophenyl.
The product of Example 3 is activated as in Example 5 and then treated with 3-(4- fluoroanilino)-l-propanol instead of N-methylbenzylamine to give the title compound.
The product of Example 68 is tteated with succinic anhydride, as published in Tetrahedron Letts. 1989, 30, 5045-48, to give the title compound.
following diradical. -CH2 H2C OCH CH O)CH9CH2-- The product of Example 3 was activated as in Example 5 and then tteated with 1,4-dioxa- 8-azaspiro[4.5]decane instead of N-methylbenzylamine to give the title compound. MS (FAB) m/z M+K = 1013.
pyridyl).
The product of Example 3 was activated as in Example 5 and then tteated with isonicotinic acid hydrazide instead of N-methylbenzylamine to give the tide compound. MS (FAB) m/z
M+K = 1007.
Example 72: Formula I: R= ethyl: n= 1: R-^R-^R^R^H: R4=OH: RI^OCH^: Rl= -0CH2C 0)RI2 (R-Configuration): RJ2= NRHRJ ; RI^H: RJJ= 3-fluorophenyl. The product of Example 3 was activated as in Example 5 and then treated with m-fluoroamline instead of N-methylbenzylamine to give the title compound. MS (FAB) m/z: M+2K-H = 1045.
The product of Example 3 was activated as in Example 5 and then tteated with rn-aminophenol instead of N-methylbenzylamine to give the title compound. MS (FAB) m/z: M+K = 979.
following diradical: -CH2CH2-NCH3-CH2CH2-.
The product of Example 3 was activated as in Example 5 and then tteated with N-methylpiperazine instead of N-methylbenzylamine to give the title compound. MS (FAB) m/z: M+H = 932.
6-(l .4-benzodioxanyl)-.
The product of Example 3 is activated as in Example 5 and then treated with l,4-benzodioxan-6-amine instead of N-methylbenzylamine to give the title compound. Example 76: Formula I: R= ethyl: n= 1 : R2=R2a=R3=R5--:H: R---=OH: RJ-^OCH^: RJ=
-0CH2C(0)RI (R-Configuration): Rl2= NRHRI5-: R14= H: RI5= 3.4-methylenedioxy- phenyl-.
The product of Example 3 is activated as in Example 5 and then tteated with
3,4-(methylenedioxy)-aniline instead of N-methylbenzylamine to give the title compound.
The product of Example 3 is activated as in Example 5 and then tteated with 1-naphthylamine instead of N-methylbenzylamine to give the title compound.
-CH9CH2CH9CH2-. thus forming a five membered ring incorporating the nitrogen to which they are attached.
The product of Example 3 is activated as in Example 5 and then tteated with pyπolidine instead of N-methylbenzylamine to provide the title compound.
-CH2CH2CH2CH2CH2-. thus forming a six membered ring incorporating the nittogen to which they are attached.
The title compound was isolated as a by-product of the reaction described in Example 6. The product was purified by HPLC (30 x 300 mm siUca column) eluting with 5:4 acetonittile/dichloromethane. Fractions containing pure product were combined and solvent removed in vacuo to give the title compound as a white foam (215.5 mg, 23% yield). MS (FAB)m/z: (M+K)=955.
-OCH2C(O)OCH2-.9-fluorenyl) (R-Configuration).
Ascomycin (10 g, .012 mol) was dissolved in distiUed CH2CI2 (50 ml). Rhodium (E) acetate dimer (100 mg) was added and the mixture cooled to 0 °C. 9-Fluorenylmethyl diazoacetate (3.35 g, .012 mol) was dissolved in CH2CI2 (10 mL) and the solution added to the reaction via syringe pump at a rate of approximately 0.5 mL/hour. Addition was complete in approximately 24 hours. The reaction was stiπed at 0 °C for an additional 24 hours then loaded onto siUca (230-400 mesh, 400 g) and the solvent evaporated by airflow in the hood. The adsorbed siUca was layered over fresh silica (800 g) in a 1 L fritted glass funnel. The silica plug was eluted with the following solvents: CH2CI2 (2 L), 3:1 CH2CI2/CH3CN (4 L), 2:1 CH2CI2/CH3CN (3 L), and 1:1 CH2CI2/CH3CN (3 L). Fractions containing product were combined and concenttated in vacuo to give 7.32 g yellow foam. Fractions containing ascomycin were combined and concentrated in vacuo to give 3.30 g green foam (contains some catalyst). The product was further purified by HPLC (siUca gel, 230-400 mesh, 50 x 500 mm column) eluting with 3.5:1 hexane/acetone at a flow rate of 80 ml/min. Fractions containg purest material were combined and concenttated in vacuo to give the title compound as a white foam (4.0 g, 45% yield based on recovered ascomycin). IR (KBr) 3440, 1740, 1710 (sh), 1650 cm" 1; MS (FAB) m/z 1066 (M+K).
Anal, calcd. for C59H8INO14O.7 H2O: C, 68.08; H, 7.98; N, 1.35. Found: C, 68.11; H, 7.88; N, 1.51.
Example 81: Formula I: R= ethyl: n= 1: R-^R-^R^R-^H: R4=OH: Rla^OCH^: Rl= -OCH2CrO)OH (R-Configuration).
The resultant product of Example 80 (5.10 g, 5 mmol) was dissolved in CH2CI2 (45 mL), whereupon piperidine (5 ml) was added. The solution was stiπed at room temperature for 2 hours then transfeπed to a separatory funnel, diluted with additional CH2CI2 (100 mL), then washed with IN HC1 (2 x 100 mL) and brine (2 x 100 mL). The organic layer was dried (Na2SO4), filtered, and the solvent removed in vacuo to give 5.08 g of a mixture of the title compound and N-(9-fluorenylmethyl)piperidine. MS (FAB) m/z 888 (M+K), 926 (M+2K- H).
The product of Example 81 (100 mg, .118 mmol) was dissolved in dichloromethane (1 mL) and the solution cooled to 0 °C. HOBTΗ2O (21.6 mg, .142 mmol) was added followed by ED AC (27.1 mg, .142 mmol) then phenethylamine (26.7 μL, .212 mmol). The reaction was warmed to room temperature and stiπed overnight. Dichloromethane (10 mL) was added and the organic phase washed with IN HC1 (2 x 20 mL), saturated bicarbonate solution (2 x 20 mL), and then brine (2 x 20 mL). The organic layer was dried (Na2SO4), filtered, and solvent removed in vacuo to give 87.5 mg yellow foam. The crude product was purified by HPLC (20 x 300 mm silica column) eluting with 2:1 hexane/acetone. Fractions containing product were combined and solvent removed in vacuo to give the title compound (49.6 mg, 44% yield) as a white solid: 93-105 °C (mp); IR (KBr) 3435, 1740, 1700, 1650 cm"1; MS (FAB) m/z 953 (M+H), 991 (M+K).
Anal, calcd. for C53H8ON2O13: C, 66.78; H, 8.46; N, 2.94. Found: C, 67.13; H, 8.33; N, 3.04. Example 83: Formula I: R= ethyl: n= 1 : R2=R2a=R3=R-l=H: R4=QH: RJ^OCH^: RJ= -0 H2C(0 R12 (R-Configuratinn): R-12= NR14R_-_S. R!^ Rv. R^= -CHlCYbC Hκ Example 82 was repeated substituting N,N-methyl, 2-phenylethyl amine for 2-phenylethylamine to provide the title compound. MS (FAB) m/z: M+K = 1005.
-0CH2C(0)R12 (R-Configuration): R±2= -HN(CH2)5_NH-dansyl.
The title compound was synthesized in the manner described for Example 82 substituting dansyl cadaverine for 2-phenylethylamine. IR (KBr) 3420, 1740, 1700, 1645 cm"1; MS (FAB) m/z 1205 (M+K).
Anal, calcd. for C62H94N4O15S: C, 63.78; H, 8.12; N, 4.80. Found: C, 63.43; H, 8.25; N, 4.48.
Example 85: Formula I: R= ethyl: n= 1: R-^R-^R^R- I: RfkpH: RJi^OCH^: RJ= -0CH2C 0)RI2 (R-Configuration): R!2= -HNCήHs.
The title compound was synthesized in the manner described for Example 82 substituting aniline for 2-phenylethylamine. 112-120 °C (mp); IR (KBr) 3440, 3400 (sh), 3300 (sh), 1740, 1700, 1650, 1540, 1500 cm"1; MS (FAB) m/z 963 (M+K).
Anal, calcd. for C51H76N2O13: C, 66.21; H, 8.28; N, 3.03. Found: C, 66.11; H, 8.15; N, 3.23.
The title compound was synthesized in the manner described for Example 5 substituting 2-(4- morphoUno)-ethylamine for N-methylbenzylamine. MS (FAB) m/z: M+H = 962.
Example 87: Formula I: R= ethyl: n= 1: R2=R2___=R3=R5=H: R4=OH: RJa=QCHr. RJ= -OCH2C O)R12 (R-Configuration): Rl2= -HN CH2 _N CH2CH2)2O- The title compound was synthesized in the manner described for Example 82 substituting 3-(4-morphoUno)-propylamine for 2-phenylethylamine. MS (FAB) m/z: M+K = 1014.
Example 88: Formula I: R= ethyl: n= 1: R2=R2a=R3=R5=H: R4=OH: RI^QCH^: RJ= -0CH2C(0)RI2 (R-Configuration): Rl2= -HN CH2 2N CH )2- The title compound was synthesized in the manner described for Example 5 substituting 2-dimethylamino-ethylamine for N-methylbenzylamine. MS (FAB) m/z: M+H = 920.
Example 89: Formula I: R= ethyl: n= 1 : R2=R__a=R =R_i=H: R4=OH: RIJ^OCH^: Rl= -0CH2C 0 R12 (R-Configuration): R-12= -HN(CH2 2N(CH2) . The title compound was synthesized in the manner described for Example 82 substituting 3-dimethylamino-propylamine for 2-phenylethylamine. MS (FAB) m/z: M+H = 934.
Example 90: Formula I: R= ethyl: n= 1: R- R^R^R- -H: R4=QH: Rl^OCH RJ= -OCH2C(O)RJ2 (R-Configuration): R-12= (S)-HNCH CH2 Hs)CO9CH2Ph. The tide compound was synthesized in the manner described for Example 82 substituting L-phenylalanine benzylester for 2-phenylethylamine. MS (FAB) m/z 1125 (M+K).
Example 91: Formula I: R= ethyl: n= 1: R-^R-^R-^R-^H: Rf^OH: Rl^OCH Rl= -0CH2C(0)R12 (R-Configuration): RJ2^ S)-HNCH CH2CfiHs)CO2H. The title compound was synthesized in the manner described in Example 3 substituting the product from Example 90 for the product from Example 2. IR (CDCI3) 1740, 1700(sh), 1645 cm'1; MS (FAB) m/z 1035 (M+K).
Example 92: Formula I: R= ethyl: n= 1: R2=R2a=R_J=R_l=H: R =OH: Rl^OCH^: Rl= -0CH2C(0)RI2 (R-Configuration): Rl2- (R)-HNCH(CH2 H )CO2CH Ph. The title compound is synthesized in the manner described for Example 82 substituting D-phenylalanine benzylester for 2-phenylethylamine.
The title compound is synthesized in the manner described in Example 3 substituting the product from Example 92 for the product from Example 2.
The product of Example 3 (1.2 g, 1.4 mmol) was dissolved in THF (4.5 mL) and the solution cooled to 0 °C before adding N-methylmorphoUne (155.1 uL, 1.4 mmol) followed by isobutyl chloroformate (122.2 uL, 1.4 mmol). The resulting suspension was stiπed for 20 minutes at 0 °C then 2-aminoethanethiol hydrochloride(320.8 mg, 2.8 mmol) was added. The mixture was stiπed for 3 h at room temperature before addition of more N- methylmorpholine (387.8 uL, 3.5 mmol). The reaction was stiπed overnight, loaded onto silica (40 mL) in a fritted funnel, then eluted with dichloromethane (100 mL), 1:1 hexane/acetone (200 mL), foUowed by acetone (100 mL). Fractions containing product were combined and solvent removed in vacuo to give 0.83 g yellow foam. The crude product was further purified by HPLC (30 x 300 mm silica column) eluting with 1.25:1 hexane/acetone to provide the title compound (320 mg, 25% yield) as a white foam. MS (FAB)m/z: (M+K)=947. Example 95: Formula I: R= ethyl: n= 1: R^R^R^R^H: R4=OH: RI^OCH^ Rl= -0CH2C 0)RI2 (R-Configuration): R-12= -HN CH2)3_SH.
The title compound is synthesized in the manner described for Example 94 substituting 3-amino-propanethiol for 2-aminoethanethiol.
Example 96: Formula I: R= ethyl: n= 1: R- R^R^R-^H: Rf^OH: RI^OCH^: R1=
Silver (I) oxide (926 mg, 4.0 mmol) was added to ascomycin (791 mg, 1.0 mmol) dissolved in acetonitrile (0.8 mL) and ethyl iodoacetate (828 μL, 7.0 mmol). Mixture was stiπed at room temperature for 3 days, removed volatiles in vacuo, and isolated product by chromatography on silica gel as described in Example 1. Spectral data were identical to those obtained for the product of Example 1.
The product of Example 3 is activated as in Example 5 and then tteated with 2-naphthylamine instead of N-methylbenzylamine to give the title compound.
-OCH2C O)OCH2Ph (R-Configuration): R4- and R5- taken together form a bond. The product of Example 2 (4.7g, 5.0 mmol) was dissolved in toluene (7.5 mL) and triethylamine (5 mL). At 0 °C methanesulfonic anhydride (2.58g, 15.0 mmol) and 4- dimethylamino-pyridine (180mg, 1.5 mmol) were added aU at once. The reaction mixture was then stiπed at ambient temperature for 18h, concenttated to constant weight invacuo, and then filtered remaining residue through sitica gel (70-230 mesh, 40 mL) eluting with hexane (1:1) until no more desired product eluted. The eluent was concenttated to dryness and further purified by HPLC on a 30x500mm column (230-400 mesh Siθ2), eluting with hexane:acetone (4:1). Fractions containing desired product were pooled and concenttated invacuo to provide the title compound (2.2 g). MS (FAB)/n/z: (M+K)=960.
-OCH2C(O)OH (R-Configuration).
The product of Example 98 (2.2g, 2.4 mmol) was dissolved in EtOH (150 mL), to which was added 10% palladium on carbon (0.22g). After shaking under hydrogen (1 atm) atmosphere for 5 hours, the catalyst was filtered from the mixture and the solution was concentrated under reduced pressure. The crude material is purified by chromatography as follows. A coarse fritted 350 mL Buchner funnel was charged with 230-400 mesh Siθ2 (175 mL). The sUica bed was wetted with CH2Cl2:i-PrOH (10:1 with 0.5% AcOH), and tamped to constant volume, whereupon a circle of filter paper was placed over the bed. A solution of the crude product in CH2Cl2:i-PrOH (10:1 with 0.5% AcOH) was then carefully loaded to the top of the column. The pad was eluted with IL of the same collecting 50 mL fractions throughout. The tide product eluted in fractions 4 and 5, which concenttated down to 924 mg. MS (FAB) m/z: M+K = 872.
Example 100: Formula I: R= ethyl: n= 1: R^R2a==R3=R4_=R_k=H: R___-=QCH;y Rl= -0CH2C(0)RI2 (R-Configuration): RI^NR-L-IRI5-. where Rl4 and RJ are taken together as the diradical: -CH2CH2OCH2CH2-.
The product of example 99 is activated as in example 5 and treated with morpholine instead of N-methylbenzylamine to give the title compound.
Example 101: Formula I: R= ethyl: n= 1: R^R2__=R2_=R£=H: R_____OH: RJ-WQCTh: R1= The product of Example 3 is activated as in Example 5 and then tteated with sulfanilamide instead of N-methylbenzylamine to give the title compound.
following diradical: -CH2CH9N CH2CH2OH)CH2CH2-. The product of Example 3 is activated as in Example 5 and then tteated with N-(2-hydroxyethyl)-piperazine instead of N-methylbenzylamine to give the tide compound.
Example 103: Formula I: R= ethyl: n= 1: R2=R2a=R2_=R_5=H: R4=OH: R-lar-QCH : Rl= The product of Example 3 was activated as in Example 5 and then tteated with N- methylaniline instead of N-methylbenzylamine to give the title compound. MS (FAB) m/z: M+K = 977.
The product of Example 3 was activated as in Example 5 and then tteated with N,N-bis- (2-hydroxyethyl)-amine instead of N-methylbenzylamine to give the title compound. MS (FAB) m/z: M+K = 975.
The product of Example 3 was activated as in Example 5 and then treated with N,N'-methyl-
(3-dimethylaminopropyl)-amine instead of N-methylbenzylamine to give the tide compound.
MS (FAB) m/z: M+H = 948.
The product of Example 3 was activated as in Example 5 and then treated with N,N- phenyl-(3-hydroxypropyl)-amine instead of N-methylbenzylamine to give the tide compound. MS (FAB) m/z: M+K = 1021.
The product of Example 3 was activated as in Example 5 and then tteated with serinol instead of N-methylbenzylamine to give the title compound. MS (FAB) m/z: M+K = 961.
The product of Example 3 was activated as in Example 5 and then tteated with 3- trifluoromethylaniline instead of N-methylbenzylamine to give the title compound. MS (FAB) m/z: M+K = 1031.
The product of Example 3 was activated as in Example 5 and then tteated with iminodiacetonitrile instead of N-methylbenzylamine to give the tide compound. MS (FAB) m/z: M+K = 965.
following diradical: -CT CTT?-.
The product of Example 3 was activated as in Example 5 and then tteated with aziridine instead of N-methylbenzylamine to give the title compound. MS (FAB) m/z: M+K = 913. Example 111: Formula I: R= ethyl: n= 1 : ^^R^R^M: R^QH- RJ^QCH;*: Rj= - CH9NH(CO)NR 4R15 (R-Configuration): Rl4 and Rl5- are taken together as the following diradical: -CH2CH2OCH2CH2-.
The product of Example 3 (0.5g, 0.58 mmol) in THF(6 mL) was stiπed together with N- methylpiperidine (146 uL, 1.2 mmol) and diphenylphosphorylazide (258 uL, 1.2 mmol) at ambient temperature for 5 minutes, then at reflux for 3h. The stirring solution was cooled to ambient temperature and treated with morphoUne (157 uL, 1.8 mmol) for 60h. The mixture was purified by HPLC on a column 20 x 300 mm (YMC 15u, 60 A spherical Siθ2) eluting with a step gradient of hexane:acetone (1:1) then hexane:acetone (2:3), to provide 440 mg (0.47 mmol) of pure title compound. MS (FAB)m/z: (M+K)=972.
The product of Example 3 was activated as in Example 111 and then tteated with aniline instead of morpholine to give the title compound. MS (FAB) m/z: M+K = 978.
The product of Example 3 is activated as in Example 111 and then tteated with benzoic acid instead of morpholine, whereupon the mixture is heated. Purification by chromatography on silica gel provides the title compound.
Example 114: Formula I: R= ethyl: n= 1: R-__-_R2a=R3=R5_=H: R4=OH: R-ii^OCHr. Rl=
Foamed ascomycin (50g, 63 mmol, crystaUine material completely dissolved in methylene chloride then concentrated to a dry foam) and benzyl iodoacetate (104g, 378 mmol, 6 eq) were mixed together, then dissolved in acetonitrile (24 mL) by stirring with an overhead mixer until homogeneous. The solution was cooled to 0 °C whereupon Ag2θ (58.4g, 252 mmol, 4 eq) was added portionwise over 15 minutes (ca. 15 additions). After complete addition and mixing (5 minutes after last addition), the ice bath was removed and the reaction allowed to stir at ambient temperature for 7 days. Diethyl ether (125 mL) was added to the reaction mixture and this was then poured over silica gel (70-230 mesh, 400 mL), mixed and allowed to air dry over night. A 3L coarse fritted Buchner funnel was charged with silica gel (70-230 mesh, 2L) and the adsorbed silica carefully layered over the fresh bed, followed by a filter paper disk. The column was eluted with CH2CI2 (4L), CH2Cl2:CH3CN (9:1, 10L), CH2Cl2:CH3CN (3:1, 8L), CH2Cl2:CH3CN (1:1, 2L), and acetone (4L), collecting IL fractions throughout. Desired product eluted in fractions 14-20 to provide a compound that was identical to the title product of Example 2 (25.6g, 27.3 mmol) as a pale yellow foam. Example 115: Formula I: R= ethyl: n= 1: R =R2a=R_i=R5=H: R4=OH: RJ^OCH RJ= The product of Example 3 was activated as in Example 111 and then treated with 3- aminopropanol instead of morpholine to give the tide compound. MS (FAB) m/z: M+K = 960.
carbomethoxymethylmercaptopurine hvdrazid-yl
The product of Example 3 was activated as in Example 5 and then tteated with 6- carbomethoxymethylmercaptopurine hydrazide instead of N-methylbenzylamine to give the tide compound.
Example 117: Formulal: R= ethyl: n= 1: R-^R-^R^R^H: R =OH: Rl^OCH^: Rl=- 0CH2C(0)R12 (R-Configuration): RI^NRHRJ-.J; R!4 and R1_5 are taken together as the following diradical: -CH2CH2SO2CH2CH2-
The product of Example 3 was activated as in Example 5 and then tteated with thiomoipholine sulf one instead of N-methylbenzylamine to give the title compound. MS (FAB) m/z: M+K = 1005.
The product of Example 3 was activated as in Example 5 and then tteated with 4- fluorophenethylamine instead of N-methylbenzylamine to give the title compound. MS (FAB) m/z: M+K = 1009.
The product of Example 3 was activated as in Example 5 and then tteated with 4- chloroaniline instead of N-methylbenzylamine to give the tide compound. MS (FAB) m/z: M+K = 997.
The product of Example 3 was activated as in Example 5 and then treated with 4- methoxyaniline instead of N-methylbenzylamine to give the tide compound. MS (FAB) m/z: M+K = 993. A solution of p-toluidine (1.03 g, 9.6 mmol) in dry THF (1 mL) was added dropwise to a stiπed solution of ethylmagnesium bromide (9.6 mmol) in dry THF (9.6 mL) at 0°C. The mixture was stiπed for 15 minutes then cooled to -78 °C before the addition of a solution of the product of Example 114 (750 mg, 0.8 mmol) in dry THF (2 mL). The mixture was stiπed for 1 hour then added dropwise to a stirring biphasic mixture of IN HCl (75 mL) and EtOAc (75 mL). The mixture was ttansfeπed to a separatory funnel, the organic layer washed with IN HCl (75 mL), saturated NaHCO3 solution (2 x 75 mL) and brine (2 x 75 mL), dried (Na2SO4), filtered, and concenttated in vacuo to give 0.93 g yellow oil. The crude material was purified by chromatography to give 385 mg of the tide compound as a white foam. MS (FAB) m/z: M+K = 977.
The product of Example 114 was tteated as in Example 121 using 3,4-dichloroaniline instead of p-toluidine to give the title compound. MS (FAB) m/z: M+K = 1031.
Example 123: Formulal: R= ethyl: n= 1: R2=R2a=R_i=R5=H: R_-_=OH: Rla^OCH Rl=- The product of Example 114 was tteated as in Example 121 using 3-iodoaniline instead of p- toluidine to give the tide compound. MS (FAB) m/z: M+K = 1088.
(a) A three-neck 2L roundbottom flask equipped with an overhead stiπer was charged with diethylether (800 mL), chloroacetyl chloride (40 mL, 0.5 mol) and (lR)-(-)-nopol (85.3 mL, 0.5 mol). At 0 °C, triethylamine (69.5 mL, 0.5 mol) was added dropwise over 15 minutes. After stirring at 0 °C for 1 hour, the mixture was warmed to ambient temperature and stiπed for 18h. The mixture was vacuum filtered through a Buchner funnel and the white cake was extracted with ether (2 x 200 mL). The filtrates were then washed sequentially with 0.5N HCl (500 mL), water (500 mL) and brine (500 mL). After drying the organics (Na2SO4), the mixture was filtered and concenttated to a lite tan oil (104 g). The resultant nopol chloroacetate was sufficiently pure to process in the next step.
(b) Sodium Iodide (20.1 g, 134 mmol) was refluxed in acetone (55 mL) for 5 minutes and cooled to room temperature. Nopol chloroacetate from step (a) (5.85 g, 24.17 mmol) was added and the reaction was stiπed for 30 minutes. The solvent was removed in vacuo and the resulting slurry was partitioned between water (30 mL) and ethyl acetate (20 mL). The aqueous portion was exttacted with additional ethyl acetate (20 mL) and the combined organics were washed sequentially with saturated sodium bicarbonate (30 mL) and 10% sodium bisulfite (30 mL); dried (sodium sulfate) and concentrated in vacuo to an amber oil (7 g). The resulting nopol iodoacetate was sufficiently pure to use in the next step.
(c) Ascomycin (2.5 g, 3.16 mmol) was foamed in a round bottom flask (See Example 114). To it was added the nopol iodoacetate from step (b) (5.70 g, 17.1 mmol, 5.4 eq) followed by acetonitrile (1.5 mL). After a homogeneous solution was obtained, it was cooled to 0 °C and sdver(I) oxide (3.13 g, 13.4 mmol) was added portionwise (15 min). The solution was brought to room temperature by gradual melting of the ice and was stiπed for 8 days. The reaction was diluted in diethyl ether and poured onto silica gel (70-230 mesh, 20 mL) and allowed to air dry. The adsorbed sUica was layered on fresh sUica (70-230 mesh, 100 mL) and eluted with methylene chloride (150 mL); methylene chloride: acetonitrile (9:1, 450 mL); (3:1, 300 mL); (1:1, 200 mL); acetone (200 mL). 50 mL fractions were collected. Fractions 11-17 contained desired crude product which was further purified by HPLC on siUca eluting with 3:1 hexane:acetone (3:1). Isolated pure tide compound (0.4 g). MS (FAB) m/z: M+K = 1036.
R1=-OCH2C(O)R12 (R-Configuration): Rl2=O-CH2-r(lR)-(+)-a-pinen-10-yl)l The product of example 124 (0.200 g, 0.201 mmol) was dissolved in dry DMF (2 mL). Imidazole (0.054 g, 0.80 mmol) was added. TMS-Cl (0.051 mL, 0.401 mmol) was added and the reaction was stined at room temperature overnight. The reaction mixture was partitioned between water (10 mL) and ethyl acetate (20 mL). The organics were washed with water (10 mL), brine (20 mL) dried (sodium sulfate) and concenttated to a faint yellow film (0.225 g). MS (FAB) m/z: M+K = 1108.
Example 126: Formulal: R= ethyl: n= 1: R2=R2a=R3-=H: R4- and R5- taken together form a
MorphoUne (0.104 mL, 1 g/mL, 1.19 mmol) was dissolved in acetonitrile (1.5 mL, dried over sieves). Trimethyl aluminum (0.60 mL of a 6 M solution in hexanes, 1.2 mmol) was added and the solution was stiπed at room temperature for 5 minutes, then cooled to 0 °C. A solution of the product from Example 125 (0.225 g, 0.210 mmol) in acetonitrile (1 mL, dried over sieves) was added dropwise and the reaction was stiπed for 3 hours. The reaction mixture was diluted in ethyl acetate (15 mL) and HCl (0.25 N, 15 mL). A thick white gel formed at the interface. The organics were washed with water (15 mL) and the aqueous portion was exttacted with additional ethyl acetate (15 mL). The combined organics were washed with brine (15 mL), dried (Na2SO4), and concentrated to a yellow oil which was purified by HPLC on silica gel and eluted with hexane:acetone (1.5:1). Yielded tide compound: 34 mg, 17%; MS (FAB) m/z: M+K = 939. Yield product of example 29: 42 mg, 22%.
Example 127: Formulal: R= ethyl: n= 1: R^R^R^H: R2a=R4 =OH: R-l^OCH Rl=-
The product of example 72 (1.0 g, 1.06 mmol) in THF (10 mL) and water (1 mL) was tteated with selenium dioxide (0.18 g, 1.59 mmol) and t-butylhydroperoxide (1.4 mL of a 3M solution in 2,2,4-trimethylpentane, 4.24 mmol). The mixture was stiπed at ambient temperature for 4 days, whereupon additional t-butylhydroperoxide solution (1.4 mL, 4.24 mmol) was added. After 2 days the reaction mixture was heated to 40 °C for 24h, then 70 °C for 48h. The solution was concenttated invacuo and purified by HPLC on siUca gel eluting with hexane:acetone (2:1). Yielded title compound: 0.18 g, 18%. MS (ESI) m/z: M+Na = 963.
Example 128: Formulal: R= ethyl: n= 1: R =R2 =R_i=R5=H: RJ=OH: Rl^OCH RJ=-
(a) A three-neck 2L roundbottom flask equipped with an overhead stirrer was charged with diethylether (800 mL), chloroacetyl chloride (40 mL, 0.5 mol) and 4-nittobenzylalcohol (76.5 g, 0.5 mol). At 0 °C, triethylamine (69.5 mL, 0.5 mol) was added dropwise over 15 minutes. After stirring at 0 °C for 1 hour, the mixture was warmed to ambient temperature and stiπed for 18h. The mixture was vacuum filtered through a Buchner funnel and the white cake was extracted with ether (2 x 200 mL). The filtrates were then washed sequentially with 0.5N HCl (500 mL), water (500 mL) and brine (500 mL). After drying the organics (Na2SO4), the mixture was filtered and concenttated to a Ute tan soUd (74.8 g). The crude product was recrystaUized from diethylether (71-72 °C)
(b) Sodium Iodide (39.5 g, 260 mmol) was refluxed in acetone (104 mL) for 3 minutes and cooled to room temperature. 4-Nittobenzyl chloroacetate from step (a) (10.7 g, 47 mmol) was added and the reaction was stiπed for 30 minutes. The solvent was removed in vacuo and the resulting sluπy was partitioned between water (50 mL) and ethyl acetate (50 mL). The aqueous portion was extracted with additional ethyl acetate (50 mL) and the combined organics were washed sequentiaUy with saturated sodium bisulfite (2 x 50 mL) and brine (50 mL). The organics were dried (sodium sulfate) and concentrated in vacuo to pure product (15.6 g).
(c) Ascomycin (5 g, 6.3 mmol) was foamed in a round bottom flask (See Example
114). To it was added the 4-nittobenzyl iodoacetate from step (b) (15.6 g, 48.6 mmol, 7.7 eq) followed by acetonittile (2.5 mL). After a homogeneous solution was obtained, it was cooled to 0 °C and sUver(I) oxide (5.9 g, 25.6 mmol) was added portionwise (15 min). The solution was brought to room temperature by gradual melting of the ice and was stiπed for 5 days. The reaction was diluted in diethyl ether (25 mL), poured onto sUica gel (70-230 mesh, 40 mL) and aUowed to air dry. The adsorbed siUca was layered on fresh silica (70-230 mesh, 200 mL) and eluted with methylene chloride (500 mL); methylene chloride:acetonitrile (9:1, 400 mL); (6:1, 300 mL); (3:1, 1000 mL); (1:1, 500 mL); (1:2, 300 mL). 100 mL fractions were coUected. Fractions containing desired product (CH2C12:CH3CN 3:1) were pooled and concentrated invacuo to provide the title compound (2.86 g, 2.9 mmol). Ascomycin was recovered in the later fractions (1.59 g, 2.0 mmol). MS (ESI) m/z: M+Na = 1007.
Example 129: Formula I: R= ethyl: n= 1: R^R-^R^R- -H: R4=OH: Rla=OCHr. Rl=
-0CH2C(0)R12 (R-Configuration): Rl2-= -NRMRH; Rli^C^bWC^CTb^O: R— -
CH2CH2QIL
The title compound was synthesized in the manner described for Example 5 substituting
N,N-[2-hydroxyethyl][2-(4-morpholino)-ethyl]amine for N-methylbenzylamine. MS (FAB) m/z: M+H = 962.
Example 130: Formula I: R= ethyl: n= 1: R2=R2 =R3=R5=H: R4=OH: Rl^OCH Rl=
-0CH2C(0)RI2 (R-Configuration): RI2= -OCH2CCK
Example 128 was repeated substituting 2,2,2-trichloroethanol for p-nittobenzylalcohol.
Example 131: In Vivo Assay of Biological Activity
The immunosuppressant activity of the compounds of the present invention was determined using the human mixed lymphocyte reaction (MLR) assay described by Kino, T. et al. in Transplantation Proceedings, XIX(5):36-39, Suppl. 6 (1987). The results of the assay, shown below in Table 1, demonstrate that the compounds tested are effective immunomodulators at sub-micromolar and, in some instances, sub-nanomolar concenttations.
It is understood that the foregoing detailed description and accompanying examples are merely illustrative and are not to be taken as Umitations upon the scope of the invention, which is defined solely by the appended claims and equivalents thereof. Variations and modifications of the disclosed embodiments wiU be apparent to those skUled in the art Such variations and modifications, including without Umitation those relating to the chemical structures, substituents, derivatives, intermediates, syntheses, formulations and/or methods of use of the invention, may be made without departing from the spirit and scope thereof.

Claims

What is claimed is:
1. A compound having the formula:
or a pharmaceutically acceptable salt, ester, amide or prodrug thereof, wherein
n is zero or one;
R is selected from the group consisting of hydrogen, methyl, ethyl, allyl, propyl, 2-hydroxyethyl, cyclopropylmethyl, 2-oxopropyl and 2-ethanal;
R1 and Rlaare selected such that one of R1 and Rla is hydrogen, -(Ci-Cδ- alkyl)oxy or hydroxy, and the other is chosen from the group consisting of: (I) -O(CH2)jC(O)R12, where j is one-to-five, and R12 is selected from the group consisting of:
(A) hydroxy;
(B) -OR13, wherein R13 is:
(i) -(Cι-Cιo-alkyl);
(ii) -(cyclo-C3-C8-alkyl);
(in) -(cyclo-C3-C8-alkyl-Cι-C3-alkyl); (iv) aryHCi- -alkyl)-, where the zero, one, two or three substituents on the aryl group, each designated R301, are independendy selected from the group consisting of:
(a) -(Cι-to-C7-alkyl);
(b) -(C2-to-C6-alkenyl);
(c) halogen;
(d) -(CH2)mNR8R9, where m is zero-to-six, and NR8R9 is either a nitrogen atom attached to R8 and R9, wherein R8 and R9 are independently selected from the group consisting of:
(1) hydrogen;
(2) -R400, wherein R400 is selected from the group consisting of: a. mod-aryl, wherein the one, two, or three substituents of mod-aryl, each designated R302, are independently selected from the group consisting of:
1. -(Ci-to-Cy-alkyl);
2. -(C2-to-C6-alkenyl);
3. halogen;
4. -(CH2)mNR1 R19, where m is as defined above and NR18R19 is either a nitrogen atom attached to R18 and R19, wherein R18 and R19 are independendy selected from the group consisting of hydrogen, -(Ci- Cζ-alkyl), unsubstituted aryl-, and unsubstituted aryl-(Cι-C6-alkyl); or NR18R19 may e a 3-to-
7-membered heterocycUc ring where the ring consists of carbon atoms, the nittogen atom shown, and zero, one or two additional heteroatoms independently selected from the group consisting of -O-, -NH-, -N(Cι-to-C6-alkyl) and -S(O)s-, wherein s is zero, one or two; 5. -CN;
6. -CHO;
7. mono-, di-, tri-, or perhalogenated
-Ci-Cβ-alkyl;
8. -S(O)sR18, where s and R18 are as defined above;
9. -C(O)NR18R19, where NR1 R19 is as defined above;
10. -(CH2)mOR18, where m and R18 are as defined above;
11. -CH(OR16)(ORl7), where Rl6 and R17 are independently chosen from -(Cι-to-C3 alkyl) groups or, taken together, R16 and R17 form an ethylene or propylene bridge;
12. -(CH2)mOC(O)R18, where m and R18 are as defined above;
13. -(CH2)mC(O)OR18, where m and R18 are as defined above;
14. -OR10, where R!0 is: (i) -PO(OH)O" M+, wherein M+ is a proton or a positively charged inorganic or organic counterion, (ii) -SO3"M+, wherein M+ is as defined above, (Ui) -C(O)(CH2)mC(O)O-M+, wherein m and M+ are as defined above;
15. -NO2;
16. -N3;
17. -(C2-to-C6-alkynyl);
18. -G≡C-Si(CH3)3; and
19. guanidino substituted by: a) hydrogen; b) -(Cι-C6-alkyl); c) unsubstituted aryl; d) (Cι-Cg-alkyl)-C(O)-; e) unsubstituted aryl-S(O)2; f) (Cι-C6-alkyl)-OC(O)-; g) unsubstituted aryl-(Cι-C6- alkyl)-OC(O); h) unsubstituted aryl-OC(O); or i) (Cι-C -alkyl)SO2-; or taken together, any two adjacent R302 substituents in a di- or trisubstituted mod-aryl group form a 5-, 6- or 7- membered carbocyclic ring, or a 5-, 6-, or 7-membered heterocyclic ring, wherein the ring atoms consist of carbon atoms and one or two heteroatoms independendy selected from the group consisting of -O-, -S(O)s-, where s is as defined above, and -NR18-, where R18 is as defined above; b. -Q-mod-aryl, where the divalent radical -Q- is selected from the group consisting of:
1. -(Ci-to- -alkyl)-;
2. -(C2-to-C6-alkenyl)-;
3. -(C2-to-C6-alkynyl)-;
4. -(CH2)mO-, wherein m is as defined above;
5. -O(CH2) -, wherein m is as defined above;
6. -N(R1 )C(O)-, wherein R 8 is as defined above;
7. -C(O)N(R18)-, wherein R18 is as defined above;
8. -S(O)s-, wherein s is as defined above;
9. -N(R18)-, wherein R18 is as defined above;
10. -N(R18)S(O)r, wherein t is one or two, and R18 is as defined above;
11. -S(O)tN(R 8)-, wherein t and R18 are as defined above;
12. -C(O)-;
13. -NN-; 14. -CHN-;
15. -NCH-;
16. -ONCH-; and
17. -CHNO-; c. -mod-Het, where the one, two, or three . substituents of mod-Het, each designated R30 , are independendy selected, and are as defined above; d. -Q-mod-Het, where Q is as defined above; e. -biaryl; f. -Q-biaryl, where Q is as defined above; g. -mod-aryl-Q-mod-aryl, where Q is as defined above; h. -mod-aryl-Q-mod-Het, where Q is as defined above; i. -mod-Het-Q-mod-aryl, where Q is as defined above; j. -mod-Het-Q-mod-Het, where Q is as defined above; k. -mod-Het-mod-aryl; 1. -mod-aryl-mod-Het; and m. -mod-Het-mod-Het;
(3) -(Ci-to-Qs-alkyl);
(4) substituted-Cι-to-C6-alkyl;
(5) -(C3-to-C6-alkenyl);
(6) substituted-C3-to-C6-alkenyl;
(7) -(C3-to-C6-alkynyl);
(8) substituted-C3-to-C6-alkynyl;
(9) -(cyclo-C3-to-Cιo-alkyl);
(10) substituted-cyclo-C3-to-Cιo-alkyl;
(11) -(cyclo-C4-to-Cιo-alkenyl);
(12) substituted-cyclo-C4-to-Cιo-alkenyl;
(13) -(bicyclo-C6-to-Cιo-alkyl);
(14) substituted-bicyclo-C6-to-Cιo-alkyl;
(15) -(bicyclo-C6-to-Cιo-alkenyl);
(16) substituted-bicyclo-C6-to-Cιo-alkenyl;
(17) -(bicyclo-C6-to-Cιo-alkenyl)-Cι-to-C6-alkyl; and (18) substituted-bicyclo-C6-to-Cιo-alkenyl-Cι-to-C6- alkyl; or -NR8R9 may be a 3- to 7-membered heterocycUc ring, where the ring consists of carbon atoms, the nittogen atom shown, and zero, one or two additional heteroatoms independently selected from the group consisting of -O-, -S(O)s-, wherein s is as defined above, and -NR8-, wherein R8 is as defined above;
(e) -CN;
(f) -CHO;
(g) mono-, di-, tri-, or perhalogenated -Cι-C6-alkyl; (h) -S(O)sR8, where s and R8 are as defined above; (i) -C(O)NR8R9, where NR8R9 is as defined above;
(j) -(CH2)mOR8, where m and R8 are as defined above; (k) -CH(OR16)(OR17), where R16 and R17 are as defined above; (1) -(CH2)mOC(O)R8, where m and R8 are as defined above; (m) -(CH2)mC(O)OR8, where m and R8 are as defined above; (n) -OR10, where R10 is as defined above; (o) -NO2;
(P) -N3;
(q) -R400, as defined above;
(r) -S(O)tNR8R9, where t and NR8R9 are as defined above;
(s) -NR8S(O)tR9, where t, R8 and R9 are as defined above;
(t) -(C2-to-C6-alkynyl);
(u) -C≡C-Si(CH3)3; and
(v) guanidino substituted by:
(1) hydrogen;
(2) -(Ci-Ce-alkyl);
(3) -mod-aryl;
(4) (C1-C8-alkyl)-C(O)-;
(5) mod-aryl-S(O)2-;
(6) (Cι-C6-alkyl)-OC(O)-;
(7) mod-aryl-(Cι-C6-alkyl)-OC(O);
(8) mod-aryl-OC(O)-; or
(9) (d- -alkyDSO^; or taken together, any two adjacent R301 substituents in a di- or trisubstituted aryl group form a 5-, 6- or 7-membered carbocycUc ring, or a 5-, 6- or 7-membered heterocyclic ring wherein the ring atoms consist of carbon atoms and zero, one or two heteroatoms independently selected from the group consisting of -O-, -S(O)s-, where s is as defined above, and -NR8-, where R8 is as defined above; with the proviso that each R301 substituent or each ring formed by two adjacent R301 groups may comprise no more than twenty non- hydrogen atoms;
(v) aryl-;
(vi) Het-;
(vii) heterocycUc-;
(vtii) mono-, di-, tri-, or per-halogenated-Ci-Cg-alkyl-;
(ix) -(cyclo-C5-Cιo-alkenyl);
(x) -(cyclo-C5-Cιo-alkenyl-Cι-C3-alkyl);
(xi) -(bicyclo-C6-Cι2-alkenyl); or
(xii) -(bicyclo-C6-C ι2-alkenyl-Cι -C3-alkyl) ; (C) -NR14R15, wherein NR14R15 is either a nitrogen atom attached to R14 and R15, wherein R14 and R15 are independently selected from the group consisting of:
(i) hydrogen;
(ii) -R4°0 , as defined above;
(iii) -(Ci-to-Cio-alkyl);
(iv) sub-Ci-to-Cio-alkyl;
(v) -(cyclo-C3-to-Cιo-alkyl);
(vi) sub-cyclo-C3-to-Cιo-alkyl;
(vii) -(cyclo-C3-to-Cιo-alkyl-Cι-to-C3-alkyl);
(viii) sub-cyclo-C3-to-Cιo-alkyl-Cι-to-C3-alkyl;
(ix) -(C3-to-Cιo-alkenyl);
(x) sub-C3-to-Cιo-alkenyl;
(xi) -(cyclo- -to-Cio-alkenyl);
(xii) sub-cyclo-C4-to-Cιo-alkenyl;
(xiii) -(cyclo-C6-to-Cιo-alkyl-C3-C5-alkenyl);
(xiv) sub-cyclo-C6-to-Cιo-alkyl-C3-C5-alkenyl;
(xv) -(C3-to-Cι0-alkynyl);
(xvi) sub-C3-to-Cιo-alkynyl;
(xvii) -(cyclo-C6-to-Cιo-alkyl-C3-C5-alkynyl);
(xviii) sub-cyclo-C6-to-Cιo-alkyl-C3-C5-alkynyl;
(xix) -(bicyclo-Cg-to-Cjo-alkyl); (xx) sub-bicyclo- -to-Cio-alkyl;
(xxi) -(bicyclo-C6-to-Cιo-alkenyl);
(xxii) sub-bicyclo-C6-to-Cιo-aikenyl;
(xxiii) -aryl;
(xxiv) -Het; and
(xxv) R6, where R6 is selected from the group consisting of:
(a) hydrogen;
(b) -(Cι-to-Cιo-alkyl);
(c) mod-Ci-to-Cio-alkyl;
(d) -(C3-to-Cιo-alkenyl);
(e) mod-C3-to-Cιo-alkenyl;
(f) -(C3-to-Cιo alkynyl);
(g) mod-C3-to-Cιo-alkynyl; (h) -(cyclo-C3-to-Cιo-alkyl); (i) mod-cyclo-C3-to-Cιo-alkyl; (j) -(cyclo-C4-to-Cιo-alkenyl); (k) mod-cyclo-C4-to-Cιo-alkenyl; (1) -(bicyclo-C6-to-Cιo-alkyl); (m) mod-bicyclo-C6-to-Cιo-alkyl; (n) -(bicyclo-C6-to-Cιo-alkenyl);
(o) mod-bicyclo-C6-to-Cιo-alkenyl; (p) -R8, as defined above; (q) -aryl; and (r) -Het; or -NR1 R15 may be a 3- to 7-membered heterocyclic ring, where the ring consists of carbon atoms, the nittogen atom shown, and zero, one or two additional heteroatoms independendy selected from -O-, -S(O)s-, wherein s is as defined above, and -NR8-, wherein R8 is as defined above, which ring is unsubstituted or substituted with from one-to-five compatible radicals independently selected from the group consisting of: (i) R6, as defined above;
(ii) -(CH^OR^where m and R6 are as defined above; (iii) -(CH2)mNR6R7, where m is as defined above and NR6R7 is either a nittogen atom attached to R6 and R7, wherein R6 is as defined above and R7 is independently selected from the group defining R6, or
-NR6R7 may be a 3- to 7-membered heterocyclic ring, where the ring consists of carbon atoms, the nitrogen atom shown, and zero, one, or two additional heteroatoms independently selected from the group consisting of -O-, -S(O)s-, wherein s is as defined above, and -NR8-, wherein R8 is as defined above, which ring is unsubstituted or substituted with from one-to-six compatible radicals independently selected from the group consisting of:
(a) -R8, as defined above;
(b) -(CH2)π,OR8, wherein m and R8 are as defined above;
(c) -S(O)sR8, wherein s and R8 are as defined above;
(d) -S(O)tNR8R9, wherein t and NR8R9 are as defined above;
(e) -(CH2)mNR8R9, wherein m and NR8R9 are as defined above;
(f) -SO3H;
(g) =NOR8, wherein R8 is as defined above; (h) -R400, as defined above;
(i) -aryl; (j) -Het; and
(k) -R 99, wherein R399 is selected from the group consisting of:
(1) hydroxyl;
(2) -C(O)OH;
(3) -C(O)OR8, where R8 is as defined above;
(4) -(cyclo-C3-to-C7-a_kyl);
(5) oxo;
(6) thiooxo;
(7) epoxy;
(8) halogen;
(9) -CN;
(10) -N3;
(11) -NO2;
(12) -OR10, where R10 is as defined above;
(13) -S(O)tNR8R9, wherein t and NR8R9 are as defined above;
(14) -NR8S(O)tR9, where t, R8 and R9 are as defined above;
(15) -CH(OR16)(OR17), where R and R17 are as defined above; and (16) guanidino substituted by hydrogen; -(Ci-Cg- alkyl); aryl; (Cι-C6-alkyl)CO-; aryl-SO -; (Ci- C6-alkyl)OC(O)-; aryl-(Cι-C$-alkyl)OC(0)-; aryl-OC(O)-; or (Cι-C -alkyl)-SO2-;
(iv) -C(O)OR6, where R6 is as defined above;
(v) -SO3H;
(vi) -S(O)sR6, where s and R6 are as defined above;
(vii) -S(O)tNR6R7, where t and NR6R7 are as defined above;
(vπi) =NOR6, where R6 is as defined above;
(ix) -aryl;
(x) -Het;
(xi) -R399, as defined above; and
(xii) -R400, as defined above;
(D) -aryl;
(E) Het-;
(F) mono-, di-, tri-, or per-halogenated-Ci-Cgalkyl;
(G) -N(R8)NR14R15, where R8 and NR14R15 are as defined above;
(H) -Si(Rπ)3, where each R11 is independently -(Ci-Cβ-alkyl), aryl-(Cι-C6- alkyl)-, or aryl; (I) -OSi(R11)3, where each R11 is independently as defined above; (J) -Sn(R11)3, where each R11 is independently as defined above; (K) -P(R11)2, where each R11 is independently as defined above; (L) -R14, as defined above; and (M) halogen;
(II) -O(CH )mS(O)sR12, where m, s and R12 are as defined above; (HI) -O(CH2)jCN, where j is as defined above;
(IV) -O(CH2)jC(=NOR14)R12, where j, R12 and R14 are as defined above;
(V) -O(CH2)jC(=N+(O")R1 )R12, where j, R12 and R14 are as defined above, with the proviso that R14 may not be hydrogen;
(VI) -O(CH2)jC(=NOR14)R15, where j, R14 and R15 are as defined above;
(VII) -O(CH2)jC(=N+(O-)R1 )R15, where j, R14 and R15 are as defined above, with the proviso that R14 may not be hydrogen;
(Vπi) -OC(O)O(CH2)jC(O)NR14R15, where j and NR14Rl5 are as defined above; (DC) -O(CH2)jNR6C(O)OR14, where j, R6 and R14 are as defined above;
(X) -O(CH2)jNR6C(O)NR14R15, where j, R6 and NR14Ri5 are as defined above;
(XI) -O(CH2)jNR6C(O)NR7NR14R15, where j, R6, R7 and NR14Ri5 are as defined above; (XB) -O(CH2)jNR6C(O)R14,where j, R6 and R14 are as defined above; and (Xπi) -O(CH2)jNR6C(O)OC(O)R14, where j, R6 and R14 are as defined above;
R2 and R2* are independendy hydrogen, halogen, or -OR14, wherein R14 is as defined above, or one of R2 and R2a may be hydroxy, when the other of R2 or R23 is hydrogen, or R2 and R2a taken together is oxo or thiooxo;
R3 and R4 are chosen, when R5 is hydrogen, such that one of R3 and R4 is hydrogen and the other is selected from hydrogen, hydroxy, -OCOR8, where R8 is as defined above, or -OSi(Rn)3, where each R11 is independendy as defined above, or one of R3 and R4 is joined with non-hydrogen R5 to form a C-23/C-24 bond, with the other of R3 and R4 being hydrogen, hydroxy, -OCOR8, where R8 is as defined above, or -OSi(R11)3, where each R11 is independently as defined above; and
R5 is hydrogen, or taken together with either R3 or R4, forms a C-23/C-24 bond;
with the proviso that, when R2 and R23 are both hydrogen and Rla is methyloxy, then R1 may not be a radical selected from the group consisting of:
(I)-O(CH2)jC(O)R20, where j is as defined above and R20 is selected from the group consisting of
(A) hydroxy;
(B) -OR21 where R21 is selected from the group consisting of loweralkyl, cycloalkyl, cycloalkylalkyl and qualified-arylalkyl, where quaUfied- arylalkyl is as defined above;
(C) -NR22R23 where R22 is selected from the group consisting of hydrogen, loweralkyl, quaUfied-arylalkyl, cycloalkyl and cycloalkylalkyl; and R23 is selected from the group consisting of hydrogen, loweralkyl, qualified- arylalkyl, cycloalkyl, cycloalkylalkyl, aminoalkyl, hydroxyalkyl, carboxyalkyl and thioloweralkyl; or, taken together, R22 and R23 are -(CH2)q- where q is two to five so as to form a saturated heterocycUc ring; and
(D) morpholino;
(H) -O(CH2)jC(O)N(R24)(CH2)mCH(R25)C(O)R20, where j, m and R20 are as defined above; R24 is selected from the group consisting of hydrogen, loweralkyl, qualified-arylalkyl, cycloalkyl and cycloalkylalkyl; and R25 is selected from the group consisting of hydrogen, loweralkyl, hydroxyloweralkyl, carboxyalkyl, thioloweralkyl, thioalkoxyalkyl, guanidinoalkyl, aminoalkyl and qualified- arylalkyl and, if m is other than zero, amino and amidoalkyl; or, taken together, R24 and R25 are -(CH2)p- where p is two to five;
(πi) -O(CH2)jC(O)N(R24)(CH2)mCH(R25)-C(O)N(R 6)(CH2)mlCH(R2 )-C(O)R20, where j, m, R20, R24 and R25 are as defined above; ml is zero to six; R26 is selected from the group consisting of hydrogen, loweralkyl, qualified-arylalkyl, cycloalkyl and cycloalkylalkyl; and R27 is selected from the group consisting of hydrogen, loweralkyl, hydroxyloweralkyl, carboxyalkyl, thioloweralkyl, thioalkoxyalkyl, guanidinoalkyl, aminoalkyl and qualified-arylalkyl and, if ml is other than zero, amino and amidoalkyl; or, taken together, R26 and R27 are -(CH2)p- where p is as defined above; and
(IV) -O(CH2)jC(O)N(R24)(CH2)mCH(R25)-C(O)N(R26)(CH2)mlCH(R27)-
C(O)N(R28)(CH2)m2CH(R 9)C(O)R20, where j, m, ml, R20, R24, R25, R^ and R27 are as defined above; m2 is zero to six;, R28 is selected from the group consisting of hydrogen, loweralkyl, quaUfied-arylalkyl, cycloalkyl and cycloalkylalkyl; and R29 is selected from the group consisting of hydrogen, loweralkyl, hydroxyloweralkyl, carboxyalkyl, thioloweralkyl, thioalkoxyalkyl, guanidinoalkyl, aminoalkyl and qualified-arylalkyl and, if m2 is other than zero, amino and amidoalkyl; or, taken together, R28 and R29 are -(CH2)p-, wherein p is as defined above.
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A compound according to Claim 1, having the formula:
wherein n, R, R2, R2a, R3, R4 and R5 are as defined in Claim 1 and A is a radical having a formula selected from the group consisting of:
where j, R12, R13, R14 and R15 are as defined in Claim 1.
A compound according to Claim 1, having the formula:
wherein n, R, R2, R2a, R3, R4 and R5 are as defined in Claim 1, and B is a radical having a formula selected from the group consisting of:
where j, m, R6, R14 and R15 are as defined in Claim 1. A compound according to Claim 1, having the formula:
wherein n, R, R2, R2a, R3, R4 and R5 are as defined in Claim 1, and D is a radical having a formula selected from the group consisting of :
where j, R6 and R7 are as defined in Claim 1.
5. A compound according to Claim 1, selected from the group consisting of:
a compound wherein R1 attaches to C-32 with R configuration and R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=OH; Rla=OCH3; and Rl= -OCH2C(O)OC2H5;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=OH; -OCH2C(O)OCH2C6H5;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=OH; -OCH2C(O)OH; a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= R2-=R2a=R3=R5_=H; R4=OH; Rla=OCH3; and Rl= -OCH2C(O)NHCH2Ph;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= R2=R2a=R3=R5=H; R4=OH; Rla=OCH3; and R!= -OCH2C(O)N(CH3)CH2Ph;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= -OCH C(O)NH2;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= R2=R2a=R3=R5=H; R4=OH; Rla=OCH3; and R*= -OCH2C(O)NHCH3;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= R2=R2a=R3=R5=H; R4=OH; Rla=OCH3; and Rl= -OCH2C(O)N(CH3)2;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= -OCH2C(O)NHC2H5;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= R2=R2a=R3=R5=H; R4=OH; -OCH2C(O)N(CH3)C2H5;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= -OCH2C(O)NHCH2CH2CH3;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= -OCH2C(O)N(CH3)CH2CH2CH3;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= R2=R2a=R3=R5=H; R4=OH; Rla=OCH3; and Rl= -OCH2C(O)NHCH(CH3)2;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= R2=R2a=R3=R5=H; R4=OH; Rla=OCH3; and Rl= -OCH2C(O)N(CH3)CH(CH3)2;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= R2=R2a=R3=R5=H; R4=OH; and Rl= -OCH2C(O)NH(cyclopropyl); a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R =R3=R5=H; R =OH; Rla=OCH3; and Rl= -OCH2C(O)NH(CH2CH2CH2CH3);
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R _=OH; Rl =OCH3; and R*= -OCH2C(O)N(CH3)CH2CH2CH2CH3;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; -OCH2C(O)NHCH2CH(CH3)2;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; -OCH2C(O)N(CH3)CH2CH(CH3)2;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=OH; Rla=OCH3; and Rl= -OCH2C(O)NH(cyclobutyl);
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=OH; Rla=OCH3; and Rl= -OCH2C(O)NHCH2CH2CH2CH2CH3;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=OH; Rl =OCH3; and R*= -OCH2C(O)N(CH3)CH2CH2CH2CH2CH3;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; -OCH2C(O)NHCH2CH2CH(CH3)2;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=0H; Rla=OCH3; and R*=
-OCH2C(O)N(CH3)CH2CH2CH(CH3)2;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=OH; Rl =OCH3; and Rl= -OCH2C(O)NH(cyclopentyl);
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=0H; Rla=OCH3; and R!= -OCH2C(O)NHCH2CH2CH2CH2CH2CH3; a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2= 2a=R3=R5=H; R4=0H; Rla=OCH3; and R!= -OCH2C(O)N(CH3)CH2CH2CH2CH2CH2CH3;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R =OH; Rla=OCH3; and R!= -OCH2C(O)NH(cyclohexyl);
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=OH; Rla=OCH3; and R!= -OCH2C(O)NR14Rl5, where R14 and Rl5, taken together= -CH2CH2OCH2CH2-, a six-membered ring incorporating the nittogen to which R 4 and R*5 are attached;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=OH; Rla=OCH3; and Rl= -OCH2C(O)NHCH2CH2OH;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; -OCH2C(O)NHCH2CH2CH2OH;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; -OCH2C(O)NHCH2CH2CH2CH2OH;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=OH; Rla=OCH3; and Rl= -OCH2C(O)NHCH2CH2CH2CH2CH2OH;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=OH; Rla=OCH3; and R*= -0CH2C(0)NHCH2CH2NH2;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=OH; Rla=OCH3; and R*= -OCH2C(O)NHCH2CH2CH2NH2;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; -OCH2C(O)NHCH2CH2CH2CH2NH2;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=0H; Rla=OCH3; and Rl=
-OCH2C(O)NHCH2CH2CH2CH2CH2NH2; a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; -OCH2C(O)NHCH2CO2CH2Ph;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; -OCH2C(O)NHCH2CO2H;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; -OCH2C(O)NHCH2CH2CO2CH2Ph;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=OH; Rla=OCH3; and Rl= -OCH2C(O)NHCH2CH2CO2H;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3-=R5-=H; -OCH2C(O)NHCH(CH3)CO2H (R configuration);
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=OH; Rla=OCH3; and R!= -OCH2C(O)NHCH(CH3)CO2H (S configuration);
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=OH; Rla=OCH3; and RJ=
-OCH2C(O)NHCH(CH3)CONHCH(CH3)CONHCH(CH3)CO2H, where all chiral centers in R1 are of R configuration;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R 4=OH; Rla=OCH3; and R*= -OCH2C(O)NH(3-phenyl-phenyl);
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=OH; -OCH2C(O)N(CH2CH2OH)(3-phenyl- phenyl);
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; -OCH2C(O)N{ CH2CH2N(CH3)(CH2CH2OH) } (phenyl); a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; 4=OH; Rla=OCH3; and Rl= -OCH2C(O)N{CH2CH2N(CH3)2}(phenyl);
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2_=R2a=R3=R5=H; R 4=OH; Rla=OCH3; and Rl= -OCH2C(O)N{CH2(3- pyridyl)}{CH2(3-pyridyl)};
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3-=R5=H; R 4=OH; Rla=OCH3; and Rl- -OCH2C(O)N(cyclohexyl)2;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R 4=OH; Rla=OCH3; and Rl= -OCH2C(O)NH-(4-moιpholinyl);
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=OH; Rla=OCH3; and Rl= -OCH2C(O)NH(4-thiomorpholinyl);
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=0H; Rla=OCH3; and R = -OCH2C(O)NH(4-CF3-phenyl);
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=0H; Rla=OCH3; and R = -OCH2C(O)NH(4-F-phenyl);
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=OH; Rla=OCH3; and R*= -OCH2C(O)NH{4-(4-moιpholino)- phenyl};
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=OH; Rla=OCH3; and RJ= -OCH2C(O)NH(4-HO-phenyl);
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=OH; Rla=OCH3; and Rl= -OCH2C(O)NH(3-pyridyl);
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a-=R3=R5=H; R4=OH; Rla=OCH3; and Rl= -OCH2C(O)NH(4-pyridyl);
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=OH; Rla=OCH3; and Rl= -OCH2C(O)NH(2-pyridyl); a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; 2=R2a=R3=R5=H; R4=OH; R^=OCH3; and R*= -OCH2C(O)N(CH3)CH2CH2OH;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=OH; Rl =OCH ; and RΪ= -OCH2C(O)NH(NHCO2CH3);
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; -OCH2C(O)-L-proUnocarboxamide;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=OH; Rla=OCH3; and Rx= -OCH2C(O)-D-prolinocarboxamide;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=OH; -OCH2C(O)-L-proUnol;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=OH; -OCH2C(O)-D-prolinol;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=OH; -OCH2C(O)N(CH2CH2OH)NHCO2CH3;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; -OCH2C(O)NH{3- (phenylethynyl)phenyl } ;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=OH; -OCH2C(O)N(CH2CH2CH2OH)(4- fluorophenyl);
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; -OCH2C(O)N(CH2CH2CH2OCOCH2CH2CO2H)(4-fluorophenyl);
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=0H; -OCH2C(O)NR14R15, where Rl4 and R15, taken together, are the diradical, -CH2CH2C(OCH2CH2O)CH2CH2-; a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=OH; -OCH2C(O)NHNH{CO-(4-pyridyl)};
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=OH; Rla=OCH3; and R!= -OCH2C(O)NH(3-fluorophenyl);
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=OH; -OCH2C(O)NH(3-hydroxy-phenyl);
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=OH; -OCH2C(O)NR14R15, where R14 and R!5, taken together, are the diradical, -CH2CH2-NCH3-CH2CH2-;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=OH; -OCH2C(O)NH{6-(l,4- benzodioxanyl)};
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; -OCH2C(O)NH(3,4-methylenedioxy- phenyl);
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; -OCH2C(O)NH(l-naphthalenyl);
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; and R1 = -OCH2C(O)NR14R15; where R14 and Rl5. taken together = -CH2CH2CH2CH2-, ta five-membered ring incorporating the nitrogen to which RI4 and Rl5 are attached;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; and R1 = -OCH2C(O)NR14R15; where R14 and Rl5, taken together = -CH2CH2CH2CH2CH2-, a six-membered ring incorporating the nittogen to which RI4 and R1^ are attached;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=OH; -OCH2C(O)OCH2-(9-fluorenyl); a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=OH; Rla=OCH3; and Rl= -OCH2C(O)OH;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R =OH; Rl =OCH3; and Rl= -OCH2C(O)NHCH2CH2C6H5;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R 4=OH; Rla=OCH3; and R*= -OCH2C(O)N(CH3)CH2CH2C6H5;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R 4=OH; Rl =OCH3; and Rl= -OCH2C(0)NH(CH2)5NH-dansyl;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=OH; Rla=OCH3; and R*= -OCH2C(O)NHC6H5;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2__:R2a=R3=R5=H; R4_=0H; Rla-_.0CH3; and R*= -OCH2C(O)NH(CH2)2N(CH2CH2)2O;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=0H; Rla=OCH3; and R*= -OCH2C(O)NH(CH2)3N(CH2CH2)2O;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=OH; Rla=OCH3; and Rx= -OCH2C(O)NH(CH2)2N(CH3)2;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5-=H; R4=OH; Rla=OCH3; and R!= -OCH2C(O)NH(CH2)3N(CH3)2;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=OH; Rla=OCH3; and RJ= -OCH2C(O)NHCH(CH2C6H5)CO2CH2Ph (S configuration);
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=OH; Rla=OCH3; and Rl= -OCH2C(O)NHCH(CH2C6H5)CO2H ( S configuration);
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=OH; Rla=OCH3; and R*= -OCH2C(O)NHCH(CH2C6H5)CO2CH2Ph (R configuration); a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; -OCH2C(O)NHCH(CH2C6H5)CO2H
(R configuration);
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=OH; -OCH2C(O)NH(CH2)2SH;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; -OCH2C(O)NH(CH2)3SH;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=OH; Rl =OCH3; and Rl= -OCH2C(O)OC2H5;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R 4=OH; Rla=OCH3; and R!= -OCH2C(O)NH(2-naphthyl);
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=H; Rla=oCH3; R1= -OCH2C(O)OCH2Ph; and R4 and R5, taken together, form a bond;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R4=R5=H; -OCH2C(O)OH;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R4=R5=H; Rl =OCH3; and R!= -OCH2C(O)NR1 R15, where R14 and R15, taken together, are the diradical, -CH2CH2OCH2CH2-;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=OH; -OCH2C(O)NH{4-(H2NSO2)-phenyl};
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; -OCH2C(O)NR14R15, R14 and R15; taken together, are the diradical, -CH2CH2N(CH2CH2OH)CH2CH2-;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; -OCH2C(O)N(CH3)(phenyl); a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; -OCH2C(O)N(CH2CH2OH)2;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R =OH; Rla=OCH3; and R*= -OCH2C(O)N(CH3)CH2CH2CH2N(CH3)2;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=QH; Rla=OCH3; and Rl= -OCH2C(O)N(phenyl)CH2CH2CH2OH;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=.R2a=R3=R5=H; R4=OH; Rla=OCH3; and Rl= -OCH2C(O)NH{CH(CH2OH)2);
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H. R4=0H; Rla=OCH3; and Rl= -OCH2C(O)NH{3-(CF3)-phenyl};
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=.R2__=R3=R5-=H; R4=OH; Rla=OCH3; and R!= -OCH2C(O)N(CH2CN)2;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2__=R3=R5=H. 4=OH; Rla=OCH3; and R*= -OCH2C(O)NR1 R15, where R14 and R15, taken together, form the diradical, -CH2CH2-;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R 4=OH; Rla=OCH3; and Rl= -OCH2NH(CO)NR14R15, where R14 and Ri5, taken together, form the diradical, -CH2CH2OCH2CH2-;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=0H; Rla=OCH3; and R*= -OCH2NH(CO)NH(phenyl);
configuration and, wherein R= ethyl; n= 1; -OCH2NHC(O)(phenyl);
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=OH; Rla=OCH3; and R*= -OCH2C(O)OCH2C6H5; a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H. R4=0H; -OCH2NH(CO)NHCH2CH2CH2OH;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; carbomethoxymethylmercaptopurine hydrazidyl);
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R 4=OH; and where R14 and R15, taken together, form the diradical, -CH2CH2SO2CH2CH2-;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; and R1=-OCH2C(O)NH{CH2CH2-(4-F- phenyl)};
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=0H; and R1=-OCH2C(O)NH(4-Cl-phenyl);
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; and R1=-OCH2C(O)NH{4-(OCH3)-phenyl};
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; and R1=-OCH2C(O)NH(4-CH3-phenyl);
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H. -OCH2C(O)NH(3,4-Cl2-phenyl);
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; and R1=-OCH2C(O)NH(3-I-phenyl);
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=-R3=R5=H; and R1=-OCH2C(O)O-CH2-[(lR)-(+)-alpha- pinen-10-yl)];
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=0Si(CH3)3; Rla=OCH3; and R1=-OCH2C(O)O-CH2-[(lR)-(+)-a- pinen-10-yl)]; a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=H; R4 and R5, taken together, form a bond; Rla=OCH3; and Rl=- OCH2C(O)(4-(morpholinyl));
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; and R1=-OCH2C(O)NH-(3-fluoro-phenyl); or
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4 =OH; Rla=OCH3; and R1=-OCH2C(O)O-(4-nitto-phenyl).
6. A compound according to Claim 5, selected from the group consisting of:
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=OH; Rla=OCH3; and R*= -OCH2C(O)NH2;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a-=R3=R5-=H; R4=OH; Rla=OCH3; and Rl= -OCH2C(O)NR14R15, where Rl4 and RI^ taken together= -CH2CH2OCH2CH2-, a six-membered ring incorporating the nittogen to which R 4 and R ^ are attached;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a-=R3_=R5=H; R4=OH; Rla=OCH3; and R = -OCH2C(O)NH(CH2CH2CH2OH);
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=OH; Rl =OCH3; and R!= -OCH2C(O)NHCH2CH2OH;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=OH; Rla=OCH3; and R1-- -OCH2NH(CO)NHCH2CH2CH2OH;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R 4=OH; Rla=OCH3; and R*= -OCH2NH(CO)NHCH2CH2OH;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a_=R3=R5=H; R4=OH; Rla=OCH3; and R!= -OCH2C(O)NH-(4-morpholinyl);
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R 4=OH; Rla=OCH3; and R*= -OCH2C(O)NH(4-HO-phenyl); a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2__=R3=R5=H; R4=OH; Rla=OCH3; and Rl= -OCH2NH(CO)NH(phenyl);
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=OH; Rla=OCH3; and Rl= -OCH2C(O)NH(3-hydroxy-phenyl);
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R 4=OH; -OCH2C(O)NR14R15; Rl4 and R15, taken together, are the diradical, -CH2CH2-NCH3-CH2CH2-;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=OH; Rla=OCH3; and R!= -OCH2C(O)NR14R15, where R14 and R15, taken together, are the diradical, -CH2CH2C(OCH2CH2O)CH2CH2-;
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R 4=OH; Rla=OCH3; and R!= -OCH2C(O)NHNH{CO-(4-pyridyl)};
a compound wherein R1 attaches to C-32 with R configuration and, wherein R= ethyl; n= 1; R2=R2a=R3=R5=H; R4=OH; -OCH2C(O)N(CH3)CH2CH2C6H5;
a compound wherein R1 attaches to C-32 with R configuration and, R= ethyl; n= 1; R2__.R2a=R3=R5=H; R4=OH; Rla=OCH3; R*= -OCH2C(O)N[(CH2)2N(CH2CH2)2O] [- CH2CH2OH];
a compound wherein R1 attaches to C-32 with R configuration and, R= ethyl; n= 1; R2=R2a=R3=R5=H; R 4=OH; Rla=OCH3; Rl= -OCH2C(O)OCH2CCl3; and
a compound wherein R1 attaches to C-32 with R configuration and, R= ethyl; n= 1; R2=R2a=R3=R5=H; R 4=OH; Rla=OCH3; R*= -OCH2C(O)Cl.
7. A pharmaceutical composition useful for immunomodulation comprising a therapeutically-effective amount of a compound according to Claim 1 and a i pharmaceuticaUy-acceptable carrier.
8. A pharmaceutical composition useful for treating a patient for immune- mediated organ or tissue allograft rejection, a graft-versus-host disease; an autoimmune disease, a reversible obstructive airway disease, a hyperproUferative disease, or an ischemic or inflammatory intestinal or bowel disease; comprising a therapeutically-effective amount of a compound of Claim 1 in combination with a pharmaceutically-acceptable carrier.
9. A method of treating a patient in need of immunosuppresive, antunflammatory, antimicrobial, antifungal, antiviral or antiproUferative thereapy, or for the reversal of chemotherapeutic drug resistance, comprising administering a therapeutically- effective amount of a compound of Claim 1 in combination with a pharmaceutically- acceptable carrier.
10. A method of treating a patient for the reversal or prevention of immune- mediated heart allograft rejection, kidney aUograft rejection, Uver allograft rejection, medulla ossium allograft rejection, skin allograft rejection, cornea allograft rejection, lung allograft rejection, pancreas aUograft rejection, intestinum tenue allograft rejection, limb allograft rejection, muscle allograft rejection, nervus allograft rejection, duodenum allograft rejection, smaU-bowel allograft rejection, pancreatic-islet-cell aUograft rejection, or graft-versus-host diseases brought about by meduUa ossium transplantation, comprising administering to such a patient a therapeutically-effective amount of a compound of Claim 1 in combination with a pharmaceuticaUy-acceptable carrier.
11. A method of treating a patient for rheumatoid arthritis, systemic lupus erythematosus, Hashimoto's thyroiditis, multiple sclerosis, myasthenia gravis, type I diabetes, uveitis, aUergic encephalomyeutis, glomerulonephritis, comprising administering a therapeutically-effective amount of a compound of Claim 1 in combination with a pharmaceuticaUy-acceptable carrier.
12. A method of treating a patient for reversible obstructive airway disease, or asthma comprising administering to such a patient a therapeutically-effective amount of a compound of Claim 1 in combination with a pharmaceuticaUy-acceptable carrier.
13. A method of treating a patient for psoriasis, atopical dermatitis, contact dermatitis, eczematous dermatitises, seboπhoeis dermatitis, Lichen planus, Pemphigus, bullous pemphigoid, Epidermolysis bullosa, urticaria, angioedemas, vasculitides, erythemas, cutaneous eosinophiUas, acne or Alopecia areata, comprising administering to such a patient a therapeutically-effective amount of a compound of Claim 1 in combination with a pharmaceuticaUy-acceptable carrier. 14. A method of treating a patient for ischemic bowel or inflammatory bowel disease, necrotizing enterocolitis, intestinal lesions associated with thermal burns or leukotriene B4-mediated diseases, intestinal inflammations or aUergies, Coeliac diseases, proctitis, eosinophUic gastroenteritis, mastocytosis, Crohn's disease or ulcerative colitis, comprising administering to such a patient a therapeutically-effective amount of a compound of Claim 1 in combination with a pharmaceutically-acceptable caπier.
15. A method of treating a patient for intimal smooth muscle cell hypeiplasia, restenosis or vascular occlusion, independent of or following biologically- or mechanically- mediated vascular injury, comprising administering to such a patient a therapeutically- effective amount of a compound of Claim 1 in combination with a pharmaceutically- acceptable carrier.
EP94910923A 1993-03-17 1994-03-11 Macrocyclic amide and urea immunomodulators Withdrawn EP0689545A4 (en)

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US32958 1993-03-17
US14941993A 1993-11-09 1993-11-09
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