RU2014135705A - Фениколовые противобактериальные средства - Google Patents
Фениколовые противобактериальные средства Download PDFInfo
- Publication number
- RU2014135705A RU2014135705A RU2014135705A RU2014135705A RU2014135705A RU 2014135705 A RU2014135705 A RU 2014135705A RU 2014135705 A RU2014135705 A RU 2014135705A RU 2014135705 A RU2014135705 A RU 2014135705A RU 2014135705 A RU2014135705 A RU 2014135705A
- Authority
- RU
- Russia
- Prior art keywords
- alkyl
- phenyl
- optionally substituted
- pyridin
- groups
- Prior art date
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- DYUQAZSOFZSPHD-UHFFFAOYSA-N Phenylpropanol Chemical compound CCC(O)C1=CC=CC=C1 DYUQAZSOFZSPHD-UHFFFAOYSA-N 0.000 title 1
- 230000000844 anti-bacterial effect Effects 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 claims abstract 35
- 150000001875 compounds Chemical class 0.000 claims abstract 25
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract 20
- 125000005842 heteroatom Chemical group 0.000 claims abstract 19
- 229910052760 oxygen Inorganic materials 0.000 claims abstract 18
- 229910052717 sulfur Inorganic materials 0.000 claims abstract 18
- 125000004122 cyclic group Chemical group 0.000 claims abstract 9
- 229910052736 halogen Inorganic materials 0.000 claims abstract 7
- 150000002367 halogens Chemical class 0.000 claims abstract 7
- 125000000623 heterocyclic group Chemical group 0.000 claims abstract 7
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract 7
- 125000004429 atom Chemical group 0.000 claims abstract 4
- 150000003839 salts Chemical class 0.000 claims abstract 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims abstract 3
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims abstract 3
- 125000002619 bicyclic group Chemical group 0.000 claims abstract 2
- 239000000651 prodrug Substances 0.000 claims abstract 2
- 229940002612 prodrug Drugs 0.000 claims abstract 2
- -1 tetrahydro-2H-pyranyl Chemical group 0.000 claims 10
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims 5
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 claims 5
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 5
- 125000004043 oxo group Chemical group O=* 0.000 claims 4
- 229910052799 carbon Inorganic materials 0.000 claims 3
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 2
- 229910019142 PO4 Inorganic materials 0.000 claims 2
- GJVYFSZHAPTFNU-AGBJPPAESA-N [(1r,2s)-1-[4-[2-(1-aminoethyl)-1,3-thiazol-5-yl]phenyl]-2-[(2,2-difluoroacetyl)amino]-3-fluoropropyl] dihydrogen phosphate Chemical compound S1C(C(N)C)=NC=C1C1=CC=C([C@@H](OP(O)(O)=O)[C@@H](CF)NC(=O)C(F)F)C=C1 GJVYFSZHAPTFNU-AGBJPPAESA-N 0.000 claims 2
- IKEXYLNJTOOQIP-VNBFMFOSSA-N [(1r,2s)-1-[4-[6-(1-aminoethyl)pyridin-3-yl]phenyl]-2-[(2,2-difluoroacetyl)amino]-3-fluoropropyl] dihydrogen phosphate Chemical compound C1=NC(C(N)C)=CC=C1C1=CC=C([C@@H](OP(O)(O)=O)[C@@H](CF)NC(=O)C(F)F)C=C1 IKEXYLNJTOOQIP-VNBFMFOSSA-N 0.000 claims 2
- 125000002393 azetidinyl group Chemical group 0.000 claims 2
- 230000015572 biosynthetic process Effects 0.000 claims 2
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 2
- OSKYZBYGXQDRKN-UHFFFAOYSA-N fluoro propyl hydrogen phosphate Chemical compound CCCOP(O)(=O)OF OSKYZBYGXQDRKN-UHFFFAOYSA-N 0.000 claims 2
- 239000001257 hydrogen Substances 0.000 claims 2
- 125000003566 oxetanyl group Chemical group 0.000 claims 2
- 125000004430 oxygen atom Chemical group O* 0.000 claims 2
- 239000010452 phosphate Substances 0.000 claims 2
- 125000004076 pyridyl group Chemical group 0.000 claims 2
- 125000000719 pyrrolidinyl group Chemical group 0.000 claims 2
- 229910052708 sodium Inorganic materials 0.000 claims 2
- 239000011734 sodium Substances 0.000 claims 2
- 125000000335 thiazolyl group Chemical group 0.000 claims 2
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 1
- IHUZDFPYYYTTPO-HSFDIDPMSA-N 2,2-difluoro-n-[(1r,2s)-3-fluoro-1-hydroxy-1-[4-(6-pyrrolidin-2-ylpyridin-3-yl)phenyl]propan-2-yl]acetamide Chemical compound C1=CC([C@H]([C@@H](CF)NC(=O)C(F)F)O)=CC=C1C1=CC=C(C2NCCC2)N=C1 IHUZDFPYYYTTPO-HSFDIDPMSA-N 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- VJSPKIYWPNYHQQ-AGBJPPAESA-N [(1r,2s)-1-[4-[2-(1-aminoethyl)-1,3-thiazol-5-yl]phenyl]-2-[(2,2-dichloroacetyl)amino]-3-fluoropropyl] dihydrogen phosphate Chemical compound S1C(C(N)C)=NC=C1C1=CC=C([C@@H](OP(O)(O)=O)[C@@H](CF)NC(=O)C(Cl)Cl)C=C1 VJSPKIYWPNYHQQ-AGBJPPAESA-N 0.000 claims 1
- DAXSSOSNYMZCIM-GDBMZVCRSA-N [(1r,2s)-1-[4-[6-(1-aminocyclopropyl)pyridin-3-yl]phenyl]-2-[(2,2-dichloroacetyl)amino]-3-fluoropropyl] dihydrogen phosphate Chemical compound C=1C=C(C=2C=CC(=CC=2)[C@@H](OP(O)(O)=O)[C@@H](CF)NC(=O)C(Cl)Cl)C=NC=1C1(N)CC1 DAXSSOSNYMZCIM-GDBMZVCRSA-N 0.000 claims 1
- RQFKVJJLNRVROD-GDBMZVCRSA-N [(1r,2s)-1-[4-[6-(1-aminocyclopropyl)pyridin-3-yl]phenyl]-2-[(2,2-difluoroacetyl)amino]-3-fluoropropyl] dihydrogen phosphate Chemical compound C=1C=C(C=2C=CC(=CC=2)[C@@H](OP(O)(O)=O)[C@@H](CF)NC(=O)C(F)F)C=NC=1C1(N)CC1 RQFKVJJLNRVROD-GDBMZVCRSA-N 0.000 claims 1
- AWSKAHPIAQMGIY-VNBFMFOSSA-N [(1r,2s)-1-[4-[6-(1-aminoethyl)pyridin-3-yl]phenyl]-2-[(2,2-dichloroacetyl)amino]-3-fluoropropyl] dihydrogen phosphate Chemical compound C1=NC(C(N)C)=CC=C1C1=CC=C([C@@H](OP(O)(O)=O)[C@@H](CF)NC(=O)C(Cl)Cl)C=C1 AWSKAHPIAQMGIY-VNBFMFOSSA-N 0.000 claims 1
- JVSRXESBLUMWSS-GDBMZVCRSA-N [(1r,2s)-1-[4-[6-(3-aminooxetan-3-yl)pyridin-3-yl]phenyl]-2-[(2,2-difluoroacetyl)amino]-3-fluoropropyl] dihydrogen phosphate Chemical compound C=1C=C(C=2C=CC(=CC=2)[C@@H](OP(O)(O)=O)[C@@H](CF)NC(=O)C(F)F)C=NC=1C1(N)COC1 JVSRXESBLUMWSS-GDBMZVCRSA-N 0.000 claims 1
- LRUKCGQIXMNODC-YJEKIOLLSA-N [(1r,2s)-1-[4-[6-(azetidin-2-yl)pyridin-3-yl]phenyl]-2-[(2,2-dichloroacetyl)amino]-3-fluoropropyl] dihydrogen phosphate Chemical compound C1=CC([C@H]([C@@H](CF)NC(=O)C(Cl)Cl)OP(O)(=O)O)=CC=C1C1=CC=C(C2NCC2)N=C1 LRUKCGQIXMNODC-YJEKIOLLSA-N 0.000 claims 1
- SGUJYJCJRFAAJB-YJEKIOLLSA-N [(1r,2s)-1-[4-[6-(azetidin-2-yl)pyridin-3-yl]phenyl]-2-[(2,2-difluoroacetyl)amino]-3-fluoropropyl] dihydrogen phosphate Chemical compound C1=CC([C@H]([C@@H](CF)NC(=O)C(F)F)OP(O)(=O)O)=CC=C1C1=CC=C(C2NCC2)N=C1 SGUJYJCJRFAAJB-YJEKIOLLSA-N 0.000 claims 1
- 125000004093 cyano group Chemical group *C#N 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 1
- 125000002883 imidazolyl group Chemical group 0.000 claims 1
- 208000015181 infectious disease Diseases 0.000 claims 1
- ZLTPDFXIESTBQG-UHFFFAOYSA-N isothiazole Chemical compound C=1C=NSC=1 ZLTPDFXIESTBQG-UHFFFAOYSA-N 0.000 claims 1
- CTAPFRYPJLPFDF-UHFFFAOYSA-N isoxazole Chemical compound C=1C=NOC=1 CTAPFRYPJLPFDF-UHFFFAOYSA-N 0.000 claims 1
- 244000144972 livestock Species 0.000 claims 1
- VTLQQLOYRCBDHM-AGBJPPAESA-N n-[(1r,2s)-1-[4-[2-(1-aminoethyl)-1,3-thiazol-5-yl]phenyl]-3-fluoro-1-hydroxypropan-2-yl]-2,2-dichloroacetamide Chemical compound S1C(C(N)C)=NC=C1C1=CC=C([C@@H](O)[C@@H](CF)NC(=O)C(Cl)Cl)C=C1 VTLQQLOYRCBDHM-AGBJPPAESA-N 0.000 claims 1
- LBAAYRIYJRTQTF-AGBJPPAESA-N n-[(1r,2s)-1-[4-[2-(1-aminoethyl)-1,3-thiazol-5-yl]phenyl]-3-fluoro-1-hydroxypropan-2-yl]-2,2-difluoroacetamide Chemical compound S1C(C(N)C)=NC=C1C1=CC=C([C@@H](O)[C@@H](CF)NC(=O)C(F)F)C=C1 LBAAYRIYJRTQTF-AGBJPPAESA-N 0.000 claims 1
- ZERSEBKFMIFWIX-GDBMZVCRSA-N n-[(1r,2s)-1-[4-[6-(1-aminocyclopropyl)pyridin-3-yl]phenyl]-3-fluoro-1-hydroxypropan-2-yl]-2,2-dichloroacetamide Chemical compound C=1C=C(C=2C=CC(=CC=2)[C@@H](O)[C@@H](CF)NC(=O)C(Cl)Cl)C=NC=1C1(N)CC1 ZERSEBKFMIFWIX-GDBMZVCRSA-N 0.000 claims 1
- KYZBXCXDZYTMFR-GDBMZVCRSA-N n-[(1r,2s)-1-[4-[6-(1-aminocyclopropyl)pyridin-3-yl]phenyl]-3-fluoro-1-hydroxypropan-2-yl]-2,2-difluoroacetamide Chemical compound C=1C=C(C=2C=CC(=CC=2)[C@@H](O)[C@@H](CF)NC(=O)C(F)F)C=NC=1C1(N)CC1 KYZBXCXDZYTMFR-GDBMZVCRSA-N 0.000 claims 1
- VKKFSKNICPCULZ-VNBFMFOSSA-N n-[(1r,2s)-1-[4-[6-(1-aminoethyl)pyridin-3-yl]phenyl]-3-fluoro-1-hydroxypropan-2-yl]-2,2-dichloroacetamide Chemical compound C1=NC(C(N)C)=CC=C1C1=CC=C([C@@H](O)[C@@H](CF)NC(=O)C(Cl)Cl)C=C1 VKKFSKNICPCULZ-VNBFMFOSSA-N 0.000 claims 1
- QSFANNHIKSMUSO-VNBFMFOSSA-N n-[(1r,2s)-1-[4-[6-(1-aminoethyl)pyridin-3-yl]phenyl]-3-fluoro-1-hydroxypropan-2-yl]-2,2-difluoroacetamide Chemical compound C1=NC(C(N)C)=CC=C1C1=CC=C([C@@H](O)[C@@H](CF)NC(=O)C(F)F)C=C1 QSFANNHIKSMUSO-VNBFMFOSSA-N 0.000 claims 1
- USTCFFKNZFMCDO-GDBMZVCRSA-N n-[(1r,2s)-1-[4-[6-(3-aminooxetan-3-yl)pyridin-3-yl]phenyl]-3-fluoro-1-hydroxypropan-2-yl]-2,2-dichloroacetamide Chemical compound C=1C=C(C=2C=CC(=CC=2)[C@@H](O)[C@@H](CF)NC(=O)C(Cl)Cl)C=NC=1C1(N)COC1 USTCFFKNZFMCDO-GDBMZVCRSA-N 0.000 claims 1
- WJFRZADFFVECLH-GDBMZVCRSA-N n-[(1r,2s)-1-[4-[6-(3-aminooxetan-3-yl)pyridin-3-yl]phenyl]-3-fluoro-1-hydroxypropan-2-yl]-2,2-difluoroacetamide Chemical compound C=1C=C(C=2C=CC(=CC=2)[C@@H](O)[C@@H](CF)NC(=O)C(F)F)C=NC=1C1(N)COC1 WJFRZADFFVECLH-GDBMZVCRSA-N 0.000 claims 1
- KPKIQCIRYDXCNL-YJEKIOLLSA-N n-[(1r,2s)-1-[4-[6-(azetidin-2-yl)pyridin-3-yl]phenyl]-3-fluoro-1-hydroxypropan-2-yl]-2,2-dichloroacetamide Chemical compound C1=CC([C@H]([C@@H](CF)NC(=O)C(Cl)Cl)O)=CC=C1C1=CC=C(C2NCC2)N=C1 KPKIQCIRYDXCNL-YJEKIOLLSA-N 0.000 claims 1
- WCUGNSPOHCLJPO-YJEKIOLLSA-N n-[(1r,2s)-1-[4-[6-(azetidin-2-yl)pyridin-3-yl]phenyl]-3-fluoro-1-hydroxypropan-2-yl]-2,2-difluoroacetamide Chemical compound C1=CC([C@H]([C@@H](CF)NC(=O)C(F)F)O)=CC=C1C1=CC=C(C2NCC2)N=C1 WCUGNSPOHCLJPO-YJEKIOLLSA-N 0.000 claims 1
- CNZXONYXJKAYJZ-IAGOWNOFSA-N n-[[5-[4-[(1r,2s)-3-fluoro-1-hydroxy-2-(methanesulfonamido)propyl]phenyl]pyridin-2-yl]methyl]methanesulfonamide Chemical compound C1=NC(CNS(=O)(=O)C)=CC=C1C1=CC=C([C@@H](O)[C@@H](CF)NS(C)(=O)=O)C=C1 CNZXONYXJKAYJZ-IAGOWNOFSA-N 0.000 claims 1
- 125000001715 oxadiazolyl group Chemical group 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- 125000003373 pyrazinyl group Chemical group 0.000 claims 1
- PBMFSQRYOILNGV-UHFFFAOYSA-N pyridazine Chemical compound C1=CC=NN=C1 PBMFSQRYOILNGV-UHFFFAOYSA-N 0.000 claims 1
- 125000000714 pyrimidinyl group Chemical group 0.000 claims 1
- 125000001113 thiadiazolyl group Chemical group 0.000 claims 1
- 125000001544 thienyl group Chemical group 0.000 claims 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 2
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/553—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having one nitrogen atom as the only ring hetero atom
- C07F9/576—Six-membered rings
- C07F9/58—Pyridine rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/425—Thiazoles
- A61K31/426—1,3-Thiazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4418—Non condensed pyridines; Hydrogenated derivatives thereof having a carbocyclic group directly attached to the heterocyclic ring, e.g. cyproheptadine
-
- 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
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/06—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom containing only hydrogen and carbon atoms in addition to the ring nitrogen atom
- C07D213/16—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom containing only hydrogen and carbon atoms in addition to the ring nitrogen atom containing only one pyridine ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/36—Radicals substituted by singly-bound nitrogen atoms
- C07D213/38—Radicals substituted by singly-bound nitrogen atoms having only hydrogen or hydrocarbon radicals attached to the substituent nitrogen atom
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/36—Radicals substituted by singly-bound nitrogen atoms
- C07D213/40—Acylated substituent nitrogen atom
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/26—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
- C07D241/02—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings
- C07D241/10—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D241/12—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/04—1,2,3-Triazoles; Hydrogenated 1,2,3-triazoles
- C07D249/06—1,2,3-Triazoles; Hydrogenated 1,2,3-triazoles with aryl radicals directly attached to ring atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
- C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
- C07D261/08—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
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Abstract
1. Соединение формулы Iили его фармацевтически приемлемые соли или пролекарства,где группировка Het представляет собой 4-14-членную циклическую или бициклическую кольцевую систему, имеющую от одного до пяти гетероатомов, выбранных из N, O и S, возможно замещенную группами Rчислом от одной до трех;каждый из Rи Rнезависимо представляет собой:a. H,b. -Cалкил, возможно замещенный одной или более чем одной группой OH, -SH, -CN, -NO, галоген, -NHR, -NCалкилR, -OCалкил, -SCалкил, -S(C=O)Салкил, -C(=O)NRR, -SOR, -SONRRили -Cциклоалкил,c. -Cциклоалкил, возможно замещенный группами Rчислом от одной до трех,d. -SOR, -C(=O)NRR, -SONRR, -C(=O)ORили -C(=O)R,e. 4-6-членную гетероциклическую кольцевую группировку, возможно имеющую от одного до четырех гетероатомов, выбранных из группы, состоящей из N, S и O, где кольцо или атом возможно замещены группами Rчислом от одной до трех, илиf. Rи R, взятые вместе с азотом, к которому они присоединены, образуют 4-11-членную циклическую или бициклическую кольцевую группировку, возможно имеющую дополнительный(е) один или два гетероатома, выбранные из группы, состоящей из N, S и O, где указанные кольцо или атом возможно замещены группами Rчислом от одной до трех;каждый из Rи Rнезависимо представляет собой:a. -H,b. -Cалкил, возможно замещенный группами OH, -SH, галоген, -CF, -CN, -NO, NH, -NHR, -NHR-OCалкил, -CH-O-CH, -SCалкил, -S(C=O)Cалкил, -C(=O)NRR, -C(=O)OH, -SONRили -SOR,c. -Cциклоалкил, возможно замещенный группами Rчислом от одной до трех,d. -C(=O)Cалкил, где алкил возможно замещен группами -S(=O)R, -SONRили -C(=O)R,e. 4-6-членную гетероциклическую кольцевую группировку, возможно имеющую от одного до трех гетероатомов, выбранных из группы, состоящей из N, S и O, где гетероциклическое кольцо возможно замещено группами Rчислом от одной до трех,f. Rи R, взятые вместе, образуют Cциклоалкил, возможно замещенный группами Rчислом от одной до трех; илиg. Rи Rвзяты вместе с одним или двумя гетероатом
Claims (24)
1. Соединение формулы I
или его фармацевтически приемлемые соли или пролекарства,
где группировка Het представляет собой 4-14-членную циклическую или бициклическую кольцевую систему, имеющую от одного до пяти гетероатомов, выбранных из N, O и S, возможно замещенную группами R6 числом от одной до трех;
каждый из R1 и R2 независимо представляет собой:
a. H,
b. -C1-8алкил, возможно замещенный одной или более чем одной группой OH, -SH, -CN, -NO2, галоген, -NHR5, -NC1-4алкилR5, -OC1-4алкил, -SC1-4алкил, -S(C=O)С1-4алкил, -C(=O)NR5R5, -SO2R5, -SO2NR5R5 или -C3-6циклоалкил,
c. -C3-8циклоалкил, возможно замещенный группами R6 числом от одной до трех,
d. -SO2R5, -C(=O)NR5R5, -SO2NR5R5, -C(=O)OR5 или -C(=O)R5,
e. 4-6-членную гетероциклическую кольцевую группировку, возможно имеющую от одного до четырех гетероатомов, выбранных из группы, состоящей из N, S и O, где кольцо или атом возможно замещены группами R6 числом от одной до трех, или
f. R1 и R2, взятые вместе с азотом, к которому они присоединены, образуют 4-11-членную циклическую или бициклическую кольцевую группировку, возможно имеющую дополнительный(е) один или два гетероатома, выбранные из группы, состоящей из N, S и O, где указанные кольцо или атом возможно замещены группами R6 числом от одной до трех;
каждый из R3 и R4 независимо представляет собой:
a. -H,
b. -C1-8алкил, возможно замещенный группами OH, -SH, галоген, -CF3, -CN, -NO2, NH2, -NHR5, -NHR5-OC1-4алкил, -CH2-O-CH3, -SC1-4алкил, -S(C=O)C1-4алкил, -C(=O)NR5R5, -C(=O)OH, -SO2NR5 или -SO2R5,
c. -C3-8циклоалкил, возможно замещенный группами R6 числом от одной до трех,
d. -C(=O)C1-8алкил, где алкил возможно замещен группами -S(=O2)R5, -SO2NR5 или -C(=O)R5,
e. 4-6-членную гетероциклическую кольцевую группировку, возможно имеющую от одного до трех гетероатомов, выбранных из группы, состоящей из N, S и O, где гетероциклическое кольцо возможно замещено группами R6 числом от одной до трех,
f. R3 и R4, взятые вместе, образуют C3-8циклоалкил, возможно замещенный группами R6 числом от одной до трех; или
g. R3 и R4 взяты вместе с одним или двумя гетероатомами, выбранными из группы, состоящей из N, S и O, с образованием оксогруппы (=O) или с образованием 4-6-членной гетероциклической кольцевой группировки, где гетероциклическое кольцо возможно замещено группами R6 числом от одной до трех; или
R1 и R3, R2 и R4, R1 и R4 или R2 и R3, взятые вместе с атомом азота, к которому они присоединены, образуют 4-6-членную гетероциклическую кольцевую группировку, возможно имеющую от одного до двух гетероатомов, выбранных из группы, состоящей из N, S и O, где гетероциклическое кольцо возможно замещено группами R6 числом от одной до трех;
в каждом случае R5 независимо представляет собой водород, C1-6алкил, -C3-6циклоалкил, NH2 или тетрагидро-2H-пиранил, где указанный алкил возможно замещен одной, двумя или тремя группами R6;
в каждом случае, R6 представляет собой H, C1-6алкил, галоген, -CN, -NO2, -CF3, -C3-6циклоалкил, оксо (=O), -NH2, -NHC1-4алкил, -N(C1-4алкил)2, -OC1-4алкил, оксо, -SH, -SC1-4алкил, -S(C=O)C1-4алкил, -SO2R5, -SONC1-4алкил, -C(=O)C1-4алкил, -C(=O)NH2, -C(=O)NHC1-4алкил, -C(=O)N(C1-4алкил)2, -NC(=O)NH2, -NC(=O)NHC1-4алкил, NC(=O)N(C1-4алкил)2, CF3 или 4-6-членную гетероциклическую кольцевую группировку, возможно имеющую от одного до четырех гетероатомов, выбранных из группы, состоящей из N, S и O;
W представляет собой -H, -PO(OH)2, -PO(OH)галоген, -CH2OPO(OH)2, -C(=O)C1-4алкил или -CH2OC(=O)C1-4алкил, где C1-4алкил возможно замещен группами -OCO2H, -OCO2C1-4алкил или -OC(=O)NHC1-4алкил;
и каждый из X, Y и Z независимо представляет собой H, галоген, C1-4алкил, C3-6циклоалкил, -OH, CF3, -NH2, -CN, N3 или -S-CF3;
при условии, что когда R3 и R4 взяты вместе с образованием оксогруппы (=O), тогда R1 и R2 оба не представляют собой водород.
2. Соединение по п. 1, где W представляет собой H, -PO(OH)2 или -CH2OPO(OH)2.
3. Соединение по п. 2, где W представляет собой H.
4. Соединение по п. 1, где X и Y представляют собой хлорид и Z представляет собой H.
5. Соединение по п. 1, где X и Y представляют собой фторид и Z представляет собой H.
6. Соединение по п. 1, где группировка Het представляет собой 5-6-членную циклическую кольцевую систему, имеющую от одного до трех гетероатомов, выбранных из N, O и S, возможно замещенную группами R6.
7. Соединение по п. 6, где группировка Het представляет собой пиридинил, тиофенил, тиазолил, тиадиазолил, имидазолил, оксадиазолил, пиримидинил, пиразинил, изоксазол, изотиазол или пиридазин.
8. Соединение по п. 7, где группировка Het представляет собой пиридинил или тиазолил.
9. Соединение по п. 1, где указанные R1 и R2 независимо представляют собой H, или R1 и R2, взятые вместе с азотом, к которому они присоединены, образуют 4-6-членную гетероциклическую кольцевую группировку, возможно имеющую дополнительный(е) один или два гетероатома, выбранных из группы, состоящей из N, S и O, где гетероциклическое кольцо возможно замещено группами R6.
10. Соединение по п. 9, где каждый из R1 и R2 представляет собой H.
11. Соединение по п. 1, где R3 и R4 независимо представляют собой H или C1-4алкил, или R3 и R4 взяты вместе с образованием C3-6циклоалкила.
12. Соединение по п. 11, где R3 и R4 взяты вместе с образованием циклопропила.
13. Соединение по п. 1, где W представляет собой H, -PO(OH)2 или -CH2OPO(OH)2; группировка Het представляет собой 5- или 6-членную циклическую кольцевую систему, имеющую от одного до трех гетероатомов, выбранных из N, O и S, возможно замещенную группами R6; каждый из R1 и R2 представляет собой H; R3 и R4 независимо представляют собой H или C1-4алкил или R3 и R4 взяты вместе с образованием циклопропила и X, Y и Z независимо представляют собой H, хлорид или фторид.
14. Соединение по п. 1, где R3 и R4 взяты вместе с одним или двумя гетероатомами, выбранными из группы, состоящей из N, S и O, с образованием 4-6-членной гетероциклической кольцевой группировки, где гетероциклическое кольцо возможно замещено группами R6 числом от одной до трех.
15. Соединение по п. 14, где R3 и R4 взяты вместе с атомом кислорода с образованием оксетанила.
16. Соединение по п. 15, где W представляет собой H или -PO(OH)2; группировка Het представляет собой 5- или 6-членную циклическую кольцевую систему, имеющую от одного до трех гетероатомов, выбранных из N, O и S, возможно замещенную группами R6; каждый из R1 и R2 представляет собой H; R3 и R4 взяты вместе с атомом кислорода с образованием оксетанила и X, Y и Z независимо представляют собой H, хлорид или фторид.
17. Соединение по п. 1, где R2 и R3 взяты вместе с атомом азота, к которому они присоединены, с образованием азетидинила.
18. Соединение по п. 17, где W представляет собой H или -PO(OH)2; группировка Het представляет собой 5- или 6-членную циклическую кольцевую систему, имеющую от одного до трех гетероатомов, выбранных из N, O и S, возможно замещенную группами R6; каждый из R1 и R4 представляет собой H; R2 и R3 взяты вместе с атомом азота, к которому они присоединены, с образованием азетидинила и X, Y и Z независимо представляют собой H, хлорид или фторид.
19. Соединение по п. 1, где R1 и R3 взяты вместе с атомом азота, к которому они присоединены, с образованием пирролидинила.
20. Соединение по п. 19, где W представляет собой H или -PO(OH)2; группировка Het представляет собой 5- или 6-членную циклическую кольцевую систему, имеющую от одного до трех гетероатомов, выбранных из N, O и S,
возможно замещенную группами R6; каждый из R2 и R4 представляет собой H; R1 и R3 взяты вместе с атомом азота, к которому они присоединены, с образованием пирролидинила; и X, Y и Z независимо представляют собой H, хлорид или фторид.
21. Соединение по п. 1, выбранное из группы, состоящей из:
N-((1R,2S)-1-(4-(2-(1-аминоэтил)тиазол-5-ил)фенил)-3-фтор-1-гидроксипропан-2-ил)-2,2-дифторацетамида;
N-((1R,2S)-1-(4-(2-(1-аминоэтил)тиазол-5-ил)фенил)-3-фтор-1-гидроксипропан-2-ил)-2,2-дихлорацетамида;
(1R,2S)-1-(4-(2-(1-аминоэтил)тиазол-5-ил)фенил)-2-(2,2-дихлорацетамидо)-3-фторпропил-гидрофосфата натрия;
(1R,2S)-1-(4-(2-(1-аминоэтил)тиазол-5-ил)фенил)-2-(2,2-дихлорацетамидо)-3-фторпропил-дигидрофосфата;
(1R,2S)-1-(4-(2-(1-аминоэтил)тиазол-5-ил)фенил)-2-(2,2-дифторацетамидо)-3-фторпропил-гидрофосфата натрия;
(1R,2S)-1-(4-(2-(1-аминоэтил)тиазол-5-ил)фенил)-2-(2,2-дифторацетамидо)-3-фторпропил-дигидрофосфата;
N-((1R,2S)-1-(4-(6-(1-аминоциклопропил)пиридин-3-ил)фенил)-3-фтор-1-гидрокси-пропан-2-ил)-2,2-дифторацетамида;
N-((1R,2S)-1-(4-(6-(1-аминоциклопропил)пиридин-3-ил)фенил)-3-фтор-1-гидрокси-пропан-2-ил)-2,2-дихлорацетамида;
(1R,2S)-1-(4-(6-(1-аминоциклопропил)пиридин-3-ил)фенил)-2-(2,2-дихлор-ацетамидо)-3-фторпропил-гидрофосфата натрия;
(1R,2S)-1-(4-(6-(1-аминоциклопропил)пиридин-3-ил)фенил)-2-(2,2-дихлор-ацетамидо)-3-фторпропил-дигидрофосфата;
(1R,2S)-1-(4-(6-(1-аминоциклопропил)пиридин-3-ил)фенил)-2-(2,2-дифтор-ацетамидо)-3-фторпропил-гидрофосфата натрия;
(1R,2S)-1-(4-(6-(1-аминоциклопропил)пиридин-3-ил)фенил)-2-(2,2-дифтор-ацетамидо)-3-фторпропил-дигидрофосфата;
N-((1R,2S)-1-(4-(6-((RS)-1-аминоэтил)пиридин-3-ил)фенил)-3-фтор-1-гидрокси-пропан-2-ил)-2,2-дифторацетамида;
N-((1R,2S)-1-(4-(6-(1-аминоэтил)пиридин-3-ил)фенил)-3-фтор-1-гидроксипропан-2-ил)-2,2-дихлорацетамида;
(1R,2S)-1-(4-(6-(1-аминоэтил)пиридин-3-ил)фенил)-2-(2,2-дихлорацетамидо)-3-фторпропил-гидрофосфата натрия;
(1R,2S)-1-(4-(6-(1-аминоэтил)пиридин-3-ил)фенил)-2-(2,2-дихлорацетамидо)-3-фторпропил-дигидрофосфата;
(1R,2S)-1-(4-(6-(1-аминоэтил)пиридин-3-ил)фенил)-2-(2,2-дифторацетамидо)-3-фторпропил-гидрофосфата натрия;
(1R,2S)-1-(4-(6-(1-аминоэтил)пиридин-3-ил)фенил)-2-(2,2-дифторацетамидо)-3-фторпропил-дигидрофосфата;
N-((1R,2S)-1-(4-(6-(азетидин-2-ил)пиридин-3-ил)фенил)-3-фтор-1-гидроксипропан-2-ил)-2,2-дифторацетамида;
N-((1R,2S)-1-(4-(6-(азетидин-2-ил)пиридин-3-ил)фенил)-3-фтор-1-гидроксипропан-2-ил)-2,2-дихлорацетамида;
(1R,2S)-1-(4-(6-(азетидин-2-ил)пиридин-3-ил)фенил)-2-(2,2-дифторацетамидо)-3-фторпропил-дигидрофосфата;
(1R,2S)-1-(4-(6-(азетидин-2-ил)пиридин-3-ил)фенил)-2-(2,2-дихлорацетамидо)-3-фторпропил-дигидрофосфата;
N-((1R,2S)-1-(4-(6-(3-аминооксетан-3-ил)пиридин-3-ил)фенил)-3-фтор-1-гидрокси-пропан-2-ил)-2,2-дифторацетамида;
(1R,2S)-1-(4-(6-(3-аминооксетан-3-ил)пиридин-3-ил)фенил)-2-(2,2-дифтор-ацетамидо)-3-фторпропил-дигидрофосфата;
(1R,2S)-1-(4-(6-(3-аминооксетан-3-ил)пиридин-3-ил)фенил)-2-(2,2-дихлор-ацетамидо)-3-фторпропил-дигидрофосфата;
N-((1R,2S)-1-(4-(6-(3-аминооксетан-3-ил)пиридин-3-ил)фенил)-3-фтор-1-гидрокси-пропан-2-ил)-2,2-дихлорацетамида;
2,2-дихлор-N-{(1S,2R)-1-(фторметил)-2-гидрокси-2-[4-(6-пирролидин-2-илпиридин-3-ил)фенил]этил}ацетамида;
(1R,2S)-2-(2,2-дихлорацетамидо)-3-фтор-1-(4-(6-(пирролидин-2-ил)пиридин-3-ил)-фенил)пропил-дигидрофосфата;
2,2-дифтор-N-{(1S,2R)-1-фторметил-2-гидрокси-2-[4-(6-пирролидин-2-ил-пиридин-3-ил)-фенил]-этил}-ацетамида; и
(1R,2S)-2-(2,2-дифторацетамидо)-3-фтор-1-(4-(6-(пирролидин-2-ил)пиридин-3-ил)-фенил)пропил-дигидрофосфата.
22. Соединение, представляющее собой N-((1R,2S)-3-фтор-1-гидрокси-1-(4-(6-(метил-сульфонамидометил)пиридин-3-ил)фенил)пропан-2-ил)метансульфонамид.
23. Фармацевтическая композиция, содержащая соединение по п. 1 или его фармацевтически приемлемую соль и фармацевтически приемлемый носитель.
24. Способ контролирования или лечения инфекций у домашнего скота, включающий введение нуждающемуся в этом животному терапевтически эффективного количества соединения по п. 1 или его фармацевтически приемлемой соли.
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