JP6735837B2 - Hiv−1阻害剤としてのc−3およびc−17修飾トリテルペノイド - Google Patents
Hiv−1阻害剤としてのc−3およびc−17修飾トリテルペノイド Download PDFInfo
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- JP6735837B2 JP6735837B2 JP2018540806A JP2018540806A JP6735837B2 JP 6735837 B2 JP6735837 B2 JP 6735837B2 JP 2018540806 A JP2018540806 A JP 2018540806A JP 2018540806 A JP2018540806 A JP 2018540806A JP 6735837 B2 JP6735837 B2 JP 6735837B2
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- ethyl
- methyl
- cyclohex
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- prop
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- 238000007918 intramuscular administration Methods 0.000 description 1
- 238000001990 intravenous administration Methods 0.000 description 1
- 230000009545 invasion Effects 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Chemical group 0.000 description 1
- 239000003456 ion exchange resin Substances 0.000 description 1
- 229920003303 ion-exchange polymer Polymers 0.000 description 1
- 229940111682 isentress Drugs 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000000904 isoindolyl group Chemical group C=1(NC=C2C=CC=CC12)* 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- FMKOJHQHASLBPH-UHFFFAOYSA-N isopropyl iodide Chemical compound CC(C)I FMKOJHQHASLBPH-UHFFFAOYSA-N 0.000 description 1
- 125000004254 isoquinolin-1-yl group Chemical group [H]C1=C([H])C2=C([H])C([H])=C([H])C([H])=C2C(*)=N1 0.000 description 1
- 125000002183 isoquinolinyl group Chemical group C1(=NC=CC2=CC=CC=C12)* 0.000 description 1
- MGIYRDNGCNKGJU-UHFFFAOYSA-N isothiazolinone Chemical compound O=C1C=CSN1 MGIYRDNGCNKGJU-UHFFFAOYSA-N 0.000 description 1
- 125000001786 isothiazolyl group Chemical group 0.000 description 1
- 125000000842 isoxazolyl group Chemical group 0.000 description 1
- 125000000468 ketone group Chemical group 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 229960001375 lactose Drugs 0.000 description 1
- 230000033001 locomotion Effects 0.000 description 1
- 229960004525 lopinavir Drugs 0.000 description 1
- 229940120922 lopinavir and ritonavir Drugs 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000003670 luciferase enzyme activity assay Methods 0.000 description 1
- 238000004020 luminiscence type Methods 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
- 229940057948 magnesium stearate Drugs 0.000 description 1
- DQEUYIQDSMINEY-UHFFFAOYSA-M magnesium;prop-1-ene;bromide Chemical compound [Mg+2].[Br-].[CH2-]C=C DQEUYIQDSMINEY-UHFFFAOYSA-M 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 239000000594 mannitol Substances 0.000 description 1
- 235000010355 mannitol Nutrition 0.000 description 1
- 229960004710 maraviroc Drugs 0.000 description 1
- 239000003550 marker Substances 0.000 description 1
- 230000001404 mediated effect Effects 0.000 description 1
- 230000002503 metabolic effect Effects 0.000 description 1
- 229940098779 methanesulfonic acid Drugs 0.000 description 1
- IZDROVVXIHRYMH-UHFFFAOYSA-N methanesulfonic anhydride Chemical compound CS(=O)(=O)OS(C)(=O)=O IZDROVVXIHRYMH-UHFFFAOYSA-N 0.000 description 1
- QARBMVPHQWIHKH-UHFFFAOYSA-N methanesulfonyl chloride Chemical compound CS(Cl)(=O)=O QARBMVPHQWIHKH-UHFFFAOYSA-N 0.000 description 1
- OSYXXQUUGMLSGE-UHFFFAOYSA-N methyl 2-methyloxirane-2-carboxylate Chemical compound COC(=O)C1(C)CO1 OSYXXQUUGMLSGE-UHFFFAOYSA-N 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- GDOPTJXRTPNYNR-UHFFFAOYSA-N methyl-cyclopentane Natural products CC1CCCC1 GDOPTJXRTPNYNR-UHFFFAOYSA-N 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 239000002808 molecular sieve Substances 0.000 description 1
- 125000002757 morpholinyl group Chemical group 0.000 description 1
- PSHKMPUSSFXUIA-UHFFFAOYSA-N n,n-dimethylpyridin-2-amine Chemical compound CN(C)C1=CC=CC=N1 PSHKMPUSSFXUIA-UHFFFAOYSA-N 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 239000007922 nasal spray Substances 0.000 description 1
- 108700004028 nef Genes Proteins 0.000 description 1
- 101150023385 nef gene Proteins 0.000 description 1
- 229960000689 nevirapine Drugs 0.000 description 1
- 125000002560 nitrile group Chemical group 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 229940042402 non-nucleoside reverse transcriptase inhibitor Drugs 0.000 description 1
- 239000002726 nonnucleoside reverse transcriptase inhibitor Substances 0.000 description 1
- 239000000346 nonvolatile oil Substances 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- 125000000962 organic group Chemical group 0.000 description 1
- 125000001715 oxadiazolyl group Chemical group 0.000 description 1
- 125000002971 oxazolyl group Chemical group 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- 230000036961 partial effect Effects 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 229940056360 penicillin g Drugs 0.000 description 1
- 239000000816 peptidomimetic Substances 0.000 description 1
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 description 1
- 239000006187 pill Substances 0.000 description 1
- 125000004193 piperazinyl group Chemical group 0.000 description 1
- 125000005936 piperidyl group Chemical group 0.000 description 1
- 125000003367 polycyclic group Chemical group 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- VVWRJUBEIPHGQF-MDZDMXLPSA-N propan-2-yl (ne)-n-propan-2-yloxycarbonyliminocarbamate Chemical compound CC(C)OC(=O)\N=N\C(=O)OC(C)C VVWRJUBEIPHGQF-MDZDMXLPSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000006239 protecting group Chemical group 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 238000000425 proton nuclear magnetic resonance spectrum Methods 0.000 description 1
- 239000012264 purified product Substances 0.000 description 1
- 125000000561 purinyl group Chemical group N1=C(N=C2N=CNC2=C1)* 0.000 description 1
- 125000004309 pyranyl group Chemical group O1C(C=CC=C1)* 0.000 description 1
- 125000003373 pyrazinyl group Chemical group 0.000 description 1
- 125000003226 pyrazolyl group Chemical group 0.000 description 1
- 125000004076 pyridyl group Chemical group 0.000 description 1
- 125000000714 pyrimidinyl group Chemical group 0.000 description 1
- 125000000168 pyrrolyl group Chemical group 0.000 description 1
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 description 1
- 229960004742 raltegravir Drugs 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 229940044551 receptor antagonist Drugs 0.000 description 1
- 239000002464 receptor antagonist Substances 0.000 description 1
- 102000005962 receptors Human genes 0.000 description 1
- 108020003175 receptors Proteins 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 229940063627 rescriptor Drugs 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 230000000284 resting effect Effects 0.000 description 1
- 238000004366 reverse phase liquid chromatography Methods 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 229940031307 selzentry Drugs 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- ACECBHHKGNTVPB-UHFFFAOYSA-N silylformic acid Chemical compound OC([SiH3])=O ACECBHHKGNTVPB-UHFFFAOYSA-N 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000000661 sodium alginate Substances 0.000 description 1
- 235000010413 sodium alginate Nutrition 0.000 description 1
- 229940005550 sodium alginate Drugs 0.000 description 1
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 1
- WRIKHQLVHPKCJU-UHFFFAOYSA-N sodium bis(trimethylsilyl)amide Chemical compound C[Si](C)(C)N([Na])[Si](C)(C)C WRIKHQLVHPKCJU-UHFFFAOYSA-N 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000012312 sodium hydride Substances 0.000 description 1
- 229910000104 sodium hydride Inorganic materials 0.000 description 1
- 235000009518 sodium iodide Nutrition 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000012321 sodium triacetoxyborohydride Substances 0.000 description 1
- 239000004334 sorbic acid Substances 0.000 description 1
- 235000010199 sorbic acid Nutrition 0.000 description 1
- 229940075582 sorbic acid Drugs 0.000 description 1
- 125000006850 spacer group Chemical group 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 229940032147 starch Drugs 0.000 description 1
- 229960005322 streptomycin Drugs 0.000 description 1
- 239000007929 subcutaneous injection Substances 0.000 description 1
- 238000010254 subcutaneous injection Methods 0.000 description 1
- 125000005346 substituted cycloalkyl group Chemical group 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 1
- BUUPQKDIAURBJP-UHFFFAOYSA-N sulfinic acid Chemical compound OS=O BUUPQKDIAURBJP-UHFFFAOYSA-N 0.000 description 1
- 239000000829 suppository Substances 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 238000003239 susceptibility assay Methods 0.000 description 1
- 239000003765 sweetening agent Substances 0.000 description 1
- 238000001308 synthesis method Methods 0.000 description 1
- 229940066769 systemic antihistamines substituted alkylamines Drugs 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- SGOIRFVFHAKUTI-ZCFIWIBFSA-N tenofovir (anhydrous) Chemical compound N1=CN=C2N(C[C@@H](C)OCP(O)(O)=O)C=NC2=C1N SGOIRFVFHAKUTI-ZCFIWIBFSA-N 0.000 description 1
- 229960004693 tenofovir disoproxil fumarate Drugs 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 125000005247 tetrazinyl group Chemical group N1=NN=NC(=C1)* 0.000 description 1
- 125000001113 thiadiazolyl group Chemical group 0.000 description 1
- 125000001984 thiazolidinyl group Chemical group 0.000 description 1
- 125000000335 thiazolyl group Chemical group 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- 125000004568 thiomorpholinyl group Chemical group 0.000 description 1
- 229960000838 tipranavir Drugs 0.000 description 1
- VXUYXOFXAQZZMF-UHFFFAOYSA-N titanium(IV) isopropoxide Chemical compound CC(C)O[Ti](OC(C)C)(OC(C)C)OC(C)C VXUYXOFXAQZZMF-UHFFFAOYSA-N 0.000 description 1
- 238000001890 transfection Methods 0.000 description 1
- 125000004306 triazinyl group Chemical group 0.000 description 1
- 125000001425 triazolyl group Chemical group 0.000 description 1
- 125000001889 triflyl group Chemical group FC(F)(F)S(*)(=O)=O 0.000 description 1
- 125000004385 trihaloalkyl group Chemical group 0.000 description 1
- PQDJYEQOELDLCP-UHFFFAOYSA-N trimethylsilane Chemical compound C[SiH](C)C PQDJYEQOELDLCP-UHFFFAOYSA-N 0.000 description 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- FTVLMFQEYACZNP-UHFFFAOYSA-N trimethylsilyl trifluoromethanesulfonate Chemical compound C[Si](C)(C)OS(=O)(=O)C(F)(F)F FTVLMFQEYACZNP-UHFFFAOYSA-N 0.000 description 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
- 229940111527 trizivir Drugs 0.000 description 1
- 230000007306 turnover Effects 0.000 description 1
- 230000029812 viral genome replication Effects 0.000 description 1
- 230000009385 viral infection Effects 0.000 description 1
- 229940098802 viramune Drugs 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
- 229940087450 zerit Drugs 0.000 description 1
- 229940052255 ziagen Drugs 0.000 description 1
Classifications
-
- 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
- A61K31/56—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
- A61K31/58—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids containing heterocyclic rings, e.g. danazol, stanozolol, pancuronium or digitogenin
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J53/00—Steroids in which the cyclopenta(a)hydrophenanthrene skeleton has been modified by condensation with a carbocyclic rings or by formation of an additional ring by means of a direct link between two ring carbon atoms, including carboxyclic rings fused to the cyclopenta(a)hydrophenanthrene skeleton are included in this class
- C07J53/002—Carbocyclic rings fused
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/14—Hydrolases (3)
- C12N9/48—Hydrolases (3) acting on peptide bonds (3.4)
- C12N9/50—Proteinases, e.g. Endopeptidases (3.4.21-3.4.25)
- C12N9/503—Proteinases, e.g. Endopeptidases (3.4.21-3.4.25) derived from viruses
- C12N9/506—Proteinases, e.g. Endopeptidases (3.4.21-3.4.25) derived from viruses derived from RNA viruses
-
- 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
- A61K31/56—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
-
- 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
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J63/00—Steroids in which the cyclopenta(a)hydrophenanthrene skeleton has been modified by expansion of only one ring by one or two atoms
- C07J63/008—Expansion of ring D by one atom, e.g. D homo steroids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2603/00—Systems containing at least three condensed rings
- C07C2603/02—Ortho- or ortho- and peri-condensed systems
- C07C2603/52—Ortho- or ortho- and peri-condensed systems containing five condensed rings
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N2740/00—Reverse transcribing RNA viruses
- C12N2740/00011—Details
- C12N2740/10011—Retroviridae
- C12N2740/16011—Human Immunodeficiency Virus, HIV
- C12N2740/16211—Human Immunodeficiency Virus, HIV concerning HIV gagpol
- C12N2740/16222—New viral proteins or individual genes, new structural or functional aspects of known viral proteins or genes
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Virology (AREA)
- Molecular Biology (AREA)
- Medicinal Chemistry (AREA)
- Zoology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Genetics & Genomics (AREA)
- Wood Science & Technology (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Biomedical Technology (AREA)
- General Engineering & Computer Science (AREA)
- Biotechnology (AREA)
- Microbiology (AREA)
- Biochemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- AIDS & HIV (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Tropical Medicine & Parasitology (AREA)
- Epidemiology (AREA)
- Steroid Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Peptides Or Proteins (AREA)
Description
Aは、-C1〜6アルキル-OR0であり、
ここでR0はヘテロアリール-Q0であり、
Q0は、-H、-CN、-C1〜6アルキル、-COOH、-Ph、-OC1〜6アルキル、-ハロ、-CF3の群から選択され、
Yは、-COOR2、-C(O)NR2SO2R3、-C(O)NHSO2NR2R2、-SO2NR2C(O)R2、-テトラゾール、及び-CONHOHの群から選択され、
R2は、-H、-C1〜6アルキル、-アルキル置換C1〜6アルキル又は-アリール置換C1〜6アルキルであり、
Wは、不在であるか、又は-CH2-若しくは-CO-であり、
R3は、-H、-C1〜6アルキル又は-アルキル置換C1〜6アルキルであり、
R4は、-H、-C1〜6アルキル、-C1〜6アルキル-C3〜6シクロアルキル、-C1〜6置換-C1〜6アルキル、-C1〜6アルキル-Q1、-C1〜6アルキル-C3〜6シクロアルキル-Q1、アリール、ヘテロアリール、置換ヘテロアリール、-COR6、-SO2R7、-SO2NR2R2、及び
ここでGは、-O-、-SO2-及び-NR12-の群から選択され、
ここでQ1は、-C1〜6アルキル、-C1〜6フルオロアルキル、ヘテロアリール、置換ヘテロアリール、ハロゲン、-CF3、-OR2、-COOR2、-NR8R9、-CONR8R9及び-SO2R7の群から選択され、
R5は、-H、-C1〜6アルキル、-C3〜6シクロアルキル、-C1〜6アルキル置換アルキル、-C1〜6アルキル-NR8R9、-COR3、-SO2R7及び-SO2NR2R2の群から選択され、
但し、R4又はR5は、Wが-CO-である場合、-COR6ではないことが条件であり、
さらに、R4又はR5の一方のみが、-COR6、-COCOR6,-SO2R7及び-SO2NR2R2の群から選択されることが条件であり、
R6は、-H、-C1〜6アルキル、-C1〜6アルキル置換アルキル、-C3〜6シクロアルキル、-C3〜6置換シクロアルキル-Q2、-C1〜6アルキル-Q2、-C1〜6アルキル置換アルキル-Q2、-C3〜6シクロアルキル-Q2、アリール-Q2、-NR13R14、及び-OR15の群から選択され、
ここでQ2はアリール、ヘテロアリール、置換ヘテロアリール、-OR2、-COOR2、-NR8R9、SO2R7、-CONHSO2R3、及び-CONHSO2NR2R2の群から選択され、
R7は、-H、-C1〜6アルキル、-C1〜6置換アルキル、-C3〜6シクロアルキル、-CF3、アリール、及びヘテロアリールの群から選択され、
R8及びR9は、-H、-C1〜6アルキル、-C1〜6置換アルキル、アリール、ヘテロアリール、置換アリール、置換ヘテロアリール、-C1〜6アルキル-Q2、及び-COOR3の群から独立して選択され、
又はR8及びR9は、隣接するNと一緒になって
Mは、-R15、-SO2R2、-SO2NR2R2、-OH及び-NR2R12の群から選択され、
Vは、-CR10R11-、-SO2-、-O-及び-NR12-の群から選択され、
但し、R8又はR9の一方のみが-COOR3であり得ることが条件であり、
R10 及びR11は、-H、-C1〜6アルキル、-C1〜6置換アルキル及び-C3〜6シクロアルキルの群から独立して選択され、
R12は、-H、-C1〜6アルキル、-アルキル置換C1〜6アルキル、-CONR2R2、-SO2R3、及び-SO2NR2R2の群から選択され、
R13及びR14は、-H、-C1〜6アルキル、-C3〜6シクロアルキル、-C1〜6置換アルキル、-C1〜6アルキル-Q3、-C1〜6アルキル-C3〜6シクロアルキル-Q3、及びC1〜6置換アルキル-Q3の群から独立して選択され、
Q3は、ヘテロアリール、置換ヘテロアリール、-NR2R12、-CONR2R2、-COOR2、-OR2、及び-SO2R3の群から選択され、
R15は、-C1〜6アルキル、-C3〜6シクロアルキル、-C1〜6置換アルキル、-C1〜6アルキル-Q3、-C1〜6アルキル-C3〜6シクロアルキル-Q3及び-C1〜6置換アルキル-Q3の群から選択され、
R16は、-H、-C1〜6アルキル、-NR2R2、及び-COOR2の群から選択され、
但し、Vが-NR12-である場合、R16が-NR2R2でないことが条件であり、
R17は、-H、-C1〜6アルキル、-COOR3、及びアリールの群から選択される]。
出願の他の部分に特定的に記載されない限り、1つ以上の以下の用語を本明細書において使用しても良く、以下の意味を有する。
Aは、-C1〜6アルキル-OR0であり、
ここでR0はヘテロアリール-Q0であり、
Q0は、-H、-CN、-C1〜6アルキル、-COOH、-Ph、-OC1〜6アルキル、-ハロ、-CF3の群から選択され、
Yは、-COOR2、-C(O)NR2SO2R3、-C(O)NHSO2NR2R2、-SO2NR2C(O)R2、-テトラゾール、及び-CONHOHの群から選択され、
R2は、-H、-C1〜6アルキル、-アルキル置換C1〜6アルキル又は-アリール置換C1〜6アルキルであり、
Wは、不在であるか、又は-CH2-若しくは-CO-であり、
R3は、-H、-C1〜6アルキル又は-アルキル置換C1〜6アルキルであり、
R4は、-H、-C1〜6アルキル、-C1〜6アルキル-C3〜6シクロアルキル、-C1〜6置換-C1〜6アルキル、-C1〜6アルキル-Q1、-C1〜6アルキル-C3〜6シクロアルキル-Q1、アリール、ヘテロアリール、置換ヘテロアリール、-COR6、-SO2R7、-SO2NR2R2、及び
ここでGは、-O-、-SO2-及び-NR12-の群から選択され、
Q1は-C1〜6アルキル、-C1〜6フルオロアルキル、ヘテロアリール、置換ヘテロアリール、ハロゲン、-CF3、-OR2、-COOR2、-NR8R9、-CONR8R9及び-SO2R7の群から選択され、
R5は、-H、-C1〜6アルキル、-C3〜6シクロアルキル、-C1〜6アルキル置換アルキル、-C1〜6アルキル-NR8R9、-COR3、-SO2R7及び-SO2NR2R2の群から選択され、
但し、R4又はR5は、Wが-CO-である場合、-COR6ではないことが条件であり、
さらに、R4又はR5の一方のみが、-COR6、-COCOR6、-SO2R7及び-SO2NR2R2の群から選択されることが条件であり、
R6は、-H、-C1〜6アルキル、-C1〜6アルキル置換アルキル、-C3〜6シクロアルキル、-C3〜6置換シクロアルキル-Q2、-C1〜6アルキル-Q2、-C1〜6アルキル置換アルキル-Q2、-C3〜6シクロアルキル-Q2、アリール-Q2、-NR13R14、及び-OR15の群から選択され、
ここでQ2はアリール、ヘテロアリール、置換ヘテロアリール、-OR2、-COOR2、-NR8R9、SO2R7、-CONHSO2R3、及び-CONHSO2NR2R2の群から選択され、
R7は、-H、-C1〜6アルキル、-C1〜6置換アルキル、-C3〜6シクロアルキル、-CF3、アリール、及びヘテロアリールの群から選択され、
R8及びR9は、-H、-C1〜6アルキル、-C1〜6置換アルキル、アリール、ヘテロアリール、置換アリール、置換ヘテロアリール、-C1〜6アルキル-Q2、及び-COOR3の群から独立して選択され、
又はR8及びR9は、隣接するNと一緒になって
Mは、-R15、-SO2R2、-SO2NR2R2、-OH及び-NR2R12の群から選択され、
Vは、-CR10R11-、-SO2-、-O-及び-NR12-の群から選択され、
但し、R8又はR9の一方のみが-COOR3であり得ることが条件であり、
R10及びR11は、-H、-C1〜6アルキル、-C1〜6置換アルキル及び-C3〜6シクロアルキルの群から独立して選択され、
R12は、-H、-C1〜6アルキル、-アルキル置換C1〜6アルキル、-CONR2R2、-SO2R3、及び-SO2NR2R2の群から選択され、
R13及びR14は、-H、-C1〜6アルキル、-C3〜6シクロアルキル、-C1〜6置換アルキル、-C1〜6アルキル-Q3、-C1〜6アルキル-C3〜6シクロアルキル-Q3、及びC1〜6置換アルキル-Q3の群から独立して選択され、
Q3は、ヘテロアリール、置換ヘテロアリール、-NR2R12、-CONR2R2、-COOR2、-OR2、及び-SO2R3の群から選択され、
R15は、-C1〜6アルキル、-C3〜6シクロアルキル、-C1〜6置換アルキル、-C1〜6アルキル-Q3、-C1〜6アルキル-C3〜6シクロアルキル-Q3及び-C1〜6置換アルキル-Q3の群から選択され、
R16は、-H、-C1〜6アルキル、-NR2R2、及び-COOR2の群から選択され、
但し、Vが-NR12-である場合、R16が-NR2R2ではないことが条件であり、
R17は、-H、-C1〜6アルキル、-COOR3、及びアリールの群から選択される。
本発明は、式Iの化合物、それらの医薬製剤及びHIV感染に罹患している又は罹患しやすい患者におけるそれらの使用を含む。式Iの化合物には、薬学的に許容されるその塩も含まれる。式Iの化合物及びそれらの合成に有用な中間体を構築する手順は、略語の後に記載されている。
1つ以上の以下の略語は、大部分が当業者に周知の慣用の略語であり、開示及び実施例の記載全体にわたって使用され得る。
RT=室温
BHT=2,6-ジ-tert-ブチル-4-ヒドロキシトルエン
CSA=ショウノウスルホン酸
LAD=リチウムジイソプロピルアミド
KHMDS=カリウムビス(トリメチルシリル)アミド
SFC=超臨界流体クロマトグラフィー
Quant=定量的
TBDMS=tert-ブチルジメチルシラン
PTFE=ポリテトラフルオロエチレン
NMO=4-メチルモルホリン-N-オキシド
THF=テトラヒドロフラン
TLC=薄層クロマトグラフィー
DCM=ジクロロメタン
DCE=ジクロロエタン
TFA=トリフルオロ酢酸
LCMS=液体クロマトグラフィー質量分析
Prep=分取
HPLC=高速液体クロマトグラフィー
DAST=(ジエチルアミノ)硫酸トリフルオリド
TEA=トリエチルアミン
DIPEA=N,N-ジイソプロピルエチルアミン
HATU=[O-(7-アザベンゾトリアゾール-1-イル)-1,1,3,3-テトラメチルウロニウムヘキサフルオロホスフェート]
DCC=N,N'-ジシクロヘキシルカルボジイミド
DMAP=ジメチルアミノピリジン
TMS=トリメチルシリル
MMR=核磁気共鳴
DPPA=ジフェニルホスホリルアジド
AIBN=アゾビスイソブチロニトリル
TBAF=フッ化テトラブチルアンモニウム
DMF=ジメチルホルムアミド
TBTU=O-(ベンゾトリアゾール-1-イル)-N,N,N',N'-テトラメチルウロニウムテトラフルオロボレート
Min=分
h=時間
sat.=飽和
TEA=トリエチルアミン
EtOAc=酢酸エチル
TFA=トリフルオロ酢酸
PCC=クロロクロム酸ピリジニウム
TLC=薄層クロマトグラフィー
Tf2NPh=(トリフルオロメチルスルホニル)メタンスルホンアミド
ジオキサン=1,4-ジオキサン
PG=保護基
atm=雰囲気
mol=モル
mmol=ミリモル
mg=ミリグラム
μg=マイクログラム
μl=マイクロリットル
μm=マイクロメートル
mm=ミリメートル
Rpm=毎分回転数
SM=出発材料
TLC=薄層クロマトグラフィー
AP=面積割合(%)
Equiv.=当量
DMP=Dess-Martinペルヨージナン
TMSCl=塩化トリメチルシリル
TBSCl=塩化tert-ブチルジメチルシリル
TBSOTf=トリフルオロメタンスルホン酸トリメチルシリル
PhMe=トルエン
PhNTf2=N-フェニル-ビス(トリフルオロメタンスルホンイミド)
S-Phos=2-ジシクロへキシルホスフィノ-2',6'-ジメトキシビフェニル
TFDO=メチル(トリフルオロメチル)ジオキシラン
TEMPO=2,2,6,6-テトラメチルピペリジニルオキシ
DI=脱イオン水
以下の実施例は、上記に一般的に記載された式Iの化合物の典型的な合成を説明する。これらの実施例は、説明のためだけのものであり、決して開示を制限することを意図しない。試薬及び出発材料は、当業者により容易に入手可能である。
選択された実施例の典型的な手順及び特徴付け:
特に記述されない限り、溶媒及び試薬は商業的供給源から得たものを直接使用し、反応は、窒素雰囲気下で実施した。フラッシュクロマトグラフィーは、シリカゲル60(粒径0.040〜0.063、EM Science supply)によって実施した。1H NMRスペクトルは、500MHzでBruker DRX-500fにより(又は記述されているように300MHzでBruker AV 400MHz、Bruker DPX-300B若しくはVarian Gemini 300により)記録した。化学シフトは、δスケールにおいてδTMS=0に対してppmで報告した。以下の内部基準を以下の溶媒中の残留プロトンのために使用した。CDCl3(δH7.26)、CD3OD(δH3.30)、酢酸-d4(酢酸d4)(δH11.6、2.07)、DMSOミックス又はDMSO-D6-CDCl3(δH2.50及び8.25)(比75%:25%)及びDMSO-D6(δH2.50)。標準的な頭字語を用いて、多重度パターンを記載した。s(一重項)、br.s(広帯一重項)、d(二重項)、t(三重項)、q(四重項)、m(多重項)、b(広帯)、app(見掛け)。カップリング定数(J)はヘルツによる。全ての液体クロマトグラフ(LC)データは、SPD-10AV UV-Vis検出器を使用してShimadzu LC-10AS液体クロマトグラフにより記録し、質量分析(MS)データは、エレクトロスプレーモードでLCのMicromass Platformを使用して決定した。
LCMS方法1
開始%B=0
最終%B=100
濃度勾配時間=2分
流速=1mL/分
波長=220nm
溶媒A=10%MeOH-90%H2O-0.1%TFA
溶媒B=90%MeOH-10%H2O-0.1%TFA
カラム=Phenomenex C18 2.0×30mm 3μm
開始%B=20
最終%B=100
濃度勾配時間=3分
流速=0.6mL/分
波長=220nm
溶媒A=10%MeOH-90%H2O-0.1%TFA
溶媒B=90%MeOH-10%H2O-0.1%TFA
カラム=Xbridge Phenyl 2.1×50mm 2.5μm
開始%B=20
最終%B=100
濃度勾配時間=2分
流速=0.6mL/分
波長=220nm
溶媒A=10%MeOH-90%H2O-0.1%TFA
溶媒B=90%MeOH-10%H2O-0.1%TFA
カラム=Xbridge Phenyl 2.1×50mm 2.5μm
開始%B=0
最終%B=100
濃度勾配時間=4分
流速=0.8mL/分
波長=220nm
溶媒A=10%MeOH-90%H2O-0.1%TFA
溶媒B=90%MeOH-10%H2O-0.1%TFA
カラム=Phenomenex C18 2.0×50mm 3μm
開始%B=20
最終%B=100
濃度勾配時間=3分
流速=0.8mL/分
波長=220nm
溶媒A=10%MeOH-90%H2O-0.1%TFA
溶媒B=90%MeOH-10%H2O-0.1%TFA
カラム=Phenomenex C18 2.0×50mm 3μm
開始%B=20
最終%B=100
濃度勾配時間=2分
流速=0.8mL/分
波長=220nm
溶媒A=10%MeOH-90%H2O-0.1%TFA
溶媒B=90%MeOH-10%H2O-0.1%TFA
カラム=Phenomenex C18 2.0×50mm 3μm
開始%B=20
最終%B=100
濃度勾配時間=2分
流速=0.5mL/分
波長=220nm
溶媒A=10%MeOH-90%H2O-0.1%TFA
溶媒B=90%MeOH-10%H2O-0.1%TFA
カラム=Xbridge Phenyl 2.1×50 mm 2.5μm
開始%B=20
最終%B=100
濃度勾配時間=2分
流速=0.8mL/分
波長=220nm
溶媒A=10%MeOH-90%H2O-0.1%TFA
溶媒B=90%MeOH-10%H2O-0.1%TFA
カラム=Xbridge Phenyl 2.1×50 mm 2.5μm
開始%B=0
最終%B=100
濃度勾配時間=2分
流速=1.0mL/分
波長=220nm
溶媒A=5%MeCN-95%H2O-10mM酢酸アンモニウム
溶媒B=95%MeCN-5%H2O-10mM酢酸アンモニウム
カラム=PHENOMENEX-LUNA C18 2.0×30mm 3μm
開始%B=0
最終%B=100
濃度勾配時間=4分
流速=0.6mL/分
波長=220nm
溶媒A=10%MeOH-90%H2O-0.1%TFA
溶媒B=90%MeOH-10%H2O-0.1%TFA
カラム=Xbridge Phenyl 2.1×50mm 2.5μm
開始%B=0
最終%B=100
濃度勾配時間=4分
流速=0.8mL/分
波長=220nm
溶媒A=10%MeOH-90%H2O-0.1%TFA
溶媒B=90%MeOH-10%H2O-0.1%TFA
カラム=Phenomenex C18 2.0×50mm 3μm
開始%B=40
最終%B=60
濃度勾配時間=4分
流速=0.8mL/分
波長=254nm
溶媒A=10%MeOH-90%H2O-0.1%TFA
溶媒B=90%MeOH-10%H2O-0.1%TFA
カラム=Xbridge Phenyl 2.1×50mm 2.5μm
開始%B=35
最終%B=100
濃度勾配時間=4分
流速=0.8mL/分
波長=220nm
溶媒A=10%MeOH-90%H2O-0.1%TFA
溶媒B=90%MeOH-10%H2O-0.1%TFA
カラム=Phenomenex C18 2.0×50mm 3μm
条件:4分かけて0%B→100%B濃度勾配、100%Bで1分間保持
溶媒A:90%水、10%メタノール、0.1%TFA
溶媒B:10%水、90%メタノール、0.1%TFA
カラム:Phenomenex Luna C18、3mm、2.0×50mm
流速:1mL/分
検出器波長:220nm
条件:2分かけて0%B→100%B濃度勾配、100%Bで1分間保持
溶媒A:90%水、10%メタノール、0.1%TFA
溶媒B:10%水、90%メタノール、0.1%TFA
カラム:Phenomenex Luna C18、2.0×50mm、3μm
流速:1mL/分
検出器波長:220nm
開始%B=2、最終%B=1.5分かけて98濃度勾配、98%Bで0.5分間保持
流速=0.8mL/分
検出器波長=220nm
溶媒A=100%水、0.05%TFA
溶媒B=100%アセトニトリル、0.05%TFA
カラム=Waters Aquity UPLC BEH C18 2.1×50mm 1.7um
オーブン温度=40℃
開始%B=2、最終%B=3分かけて98濃度勾配、98%Bで1分間保持
流速=0.8mL/分
検出器波長=220nm
溶媒A=100%水、0.05%TFA
溶媒B=100%アセトニトリル、0.05%TFA
カラム=Waters Aquity UPLC BEH C18、2.1×50mm、1.7μm
オーブン温度=40℃
開始%B=0、最終%B=4分かけて100濃度勾配、100%Bで1分間保持
流速=0.8mL/分
検出器波長=220nm
溶媒A=95%水、5%アセトニトリル、10mM酢酸アンモニウム
溶媒B=5%水、95%アセトニトリル、10mM酢酸アンモニウム
カラム=Phenomenex Luna C18、50×2mm、3μm
オーブン温度=40℃
開始%B=2、最終%B=4分かけて98濃度勾配、98%Bで1分間保持
流速=0.8mL/分
検出器波長=220nm
溶媒A=100%水、0.05%TFA
溶媒B=100%アセトニトリル、0.05%TFA
カラム=Waters Aquity UPLC BEH C18、2.1×50mm、1.7μm
オーブン温度=40℃
開始%B=2、最終%B=2分かけて98濃度勾配、98%Bで1分間保持
流速=0.8mL/分
検出器波長=220nm
溶媒A=100%水、0.05%TFA
溶媒B=100%アセトニトリル、0.05%TFA
カラム=Waters Aquity UPLC BEH C18、2.1×50mm、1.7μm
オーブン温度=40℃
開始%B=0、最終%B=2分かけて100濃度勾配、100%Bで3分間保持
流速=0.8mL/分
検出器波長=220nm
溶媒A=95%水、5%アセトニトリル、10mM酢酸アンモニウム
溶媒B=5%水、95%アセトニトリル、10mM酢酸アンモニウム
カラム=Phenomenex Luna C18、50×2mm、3μm
オーブン温度=40℃
分取HPLC方法1
条件:20分かけて30%B→100%B濃度勾配、100%Bで4分間保持
溶媒A:5%アセトニトリル、95%水、0.1%TFA
溶媒B:95%アセトニトリル、5%水、0.1%TFA
カラム:Waters Xbridge 30×100mm、5μm
流速:40mL/分
検出器波長:220nm
条件:25分かけて10%B→100%B濃度勾配
溶媒A:5%アセトニトリル、95%水、0.1%TFA
溶媒B:95%アセトニトリル、5%水、0.1%TFA
カラム:Waters Sunfire 30×150mm、5um
流速:40mL/分
検出器波長:220nm
条件:20分かけて10%B→100%B濃度勾配、100%Bで5分間保持
溶媒A:5%アセトニトリル、95%水、0.1%TFA
溶媒B:95%アセトニトリル、5%水、0.1%TFA
カラム:Waters Sunfire 30×150mm、5um
流速:40mL/分
検出器波長:220nm
条件:20分かけて30%B→100%B濃度勾配、100%Bで5分間保持
溶媒A:5%アセトニトリル、95%水、0.1%TFA
溶媒B:95%アセトニトリル、5%水、0.1%TFA
カラム:Waters Sunfire 30×150mm、5um
流速:40mL/分
検出器波長:220nm
開始%B=20、最終%B=10分かけて100濃度勾配、100%Bで4分間保持
流速=50ml/分
波長=220
溶媒対=水-アセトニトリル-TFA
溶媒A=90%水-10%アセトニトリル-0.1%TFA
溶媒B=10%水-90%アセトニトリル-0.1%TFA
カラム=Waters Sunfire C18、5μm、30×150mm
条件:20分かけて0%B→100%B濃度勾配
溶媒A:10%アセトニトリル、90%水、0.1%TFA
溶媒B:90%アセトニトリル、10%水、0.1%TFA
カラム:Waters Sunfire C18、30×150mm、5μm
流速:50mL/分
検出器波長:220nm
条件:20分かけて30%B→100%B濃度勾配
溶媒A:10%アセトニトリル、90%水、0.1%TFA
溶媒B:90%アセトニトリル、10%水、0.1%TFA
カラム:Waters Sunfire C18、30×150mm、5μm
流速:50mL/分
検出器波長:220nm
条件:15分かけて20%B→100%B濃度勾配
溶媒A:10%アセトニトリル、90%水、0.1%TFA
溶媒B:90%アセトニトリル、10%水、0.1%TFA
カラム:Waters Sunfire C18、30×150mm、5μm
流速:50mL/分
検出器波長:220nm
分取MPLC方法1
条件:30%Bで1カラム容量、30%Bから80%Bの勾配で7カラム容量、80%Bから100%Bの勾配で0.5カラム容量、100%Bで2カラム容量
溶媒A=5%アセトニトリル、95%水、0.1%TFA
溶媒B=95%アセトニトリル、5%水、0.1%TFA
カラム=Redi Sep Gold(150g)
流速=60mL/分
検出器波長=220nm
条件:30%Bで1カラム容量、30%Bから80%Bの勾配で10カラム容量、100%Bで2カラム容量
溶媒A=5%アセトニトリル、95%水、0.1%TFA
溶媒B=95%アセトニトリル、5%水、0.1%TFA
カラム=Redi Sep Gold(150g)
流速=60mL/分
検出器波長=220nm
分析的HPLC方法1
条件:15分かけて10%B→100%B濃度勾配、100%Bで10分間保持
溶媒A:10%メタノール、90%水、0.1%TFA
溶媒B:90%メタノール、10%水、0.1%TFA
カラム:Waters Sunfire C18、4.6×150mm、3.5mm
流速:1mL/分
検出器波長:220nm
条件:15分かけて10%B→100%B濃度勾配、100%Bで10分間保持
溶媒A:10%メタノール、90%水、0.1%TFA
溶媒B:90%メタノール、10%水、0.1%TFA
カラム:Waters Xbridge Phenyl、4.6×150mm、3.5mm
流速:1mL/分
検出器波長:220nm
条件:15分かけて10%B→100%B濃度勾配、100%Bで10分間保持
溶媒A:5%アセトニトリル、95%水、0.1%TFA
溶媒B:95%アセトニトリル、5%水、0.1%TFA
カラム:Waters Sunfire C18、3.0×150mm、3.5um
流速:0.5mL/分
検出器波長:220nm
条件:15分かけて10%B→100%B濃度勾配、100%Bで10分間保持
溶媒A:5%アセトニトリル、95%水、0.1%TFA
溶媒B:95%アセトニトリル、5%水、0.1%TFA
カラム:Waters Xbridge Phenyl、3.0×150mm、3.5um
流速:0.5mL/分
検出器波長:220nm
SFC実験の詳細
カラム:ChiralCel OJ-H、30×250mm、5μm
移動相:5%MeOH/95%CO2
圧力:100バール
温度:40℃
流速:70mL/分
UV:225nm
注入:0.50mL(〜100mg/mL、IPA:ACN:MeOH、2:2:1中)
フラクション収集:Slope & Level(6mL/分のMeOHで構成):
ピーク1 ウインドウ:3.00'-4.50'
ピーク2 ウインドウ:3.80'-7.00'
4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-(1,1-ジオキシドチオモルホリノ)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)-1-((ピリジン-2-イルオキシ)メチル)シクロヘキサ-3-エン-1-カルボン酸の調製
4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-(1,1-ジオキシドチオモルホリノ)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)-1-(((1-メチル-3-フェニル-1H-ピラゾール-5-イル)オキシ)メチル)シクロヘキサ-3-エン-1-カルボン酸の調製
4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-(1,1-ジオキシドチオモルホリノ)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)-1-(((1-メチル-5-(トリフルオロメチル)-1H-ピラゾール-3-イル)オキシ)メチル)シクロヘキサ-3-エン-1-カルボン酸の調製
2-((1-カルボキシ-4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-(1,1-ジオキシドチオモルホリノ)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)シクロヘキサ-3-エン-1-イル)メトキシ)チアゾール-4-カルボン酸の調製
4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-(1,1-ジオキシドチオモルホリノ)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)-1-(((4-メチル-1,2,5-チアジアゾール-3-イル)オキシ)メチル)シクロヘキサ-3-エン-1-カルボン酸の調製
1H NMR (400MHz, クロロホルム-d) δ 5.36 (br. s., 1H), 5.18 (br. s., 1H), 4.74 (br. s., 1H), 4.65 (br. s., 1H), 4.59 - 4.45 (m, 2H), 3.24 - 2.98 (m, 9H), 2.89 - 2.51 (m, 5H), 2.34 (s, 3H), 1.68 (s, 3H), 2.22 - 0.97 (m, 27H), 1.15 (s, 3H), 1.02 (s, 3H), 0.97 - 0.89 (m, 6H), 0.86 (s, 3H). LC/MS m/z 823.55 (M+H)+, 2.85分 (LCMS方法3).
1-(((1,2,5-チアジアゾール-3-イル)オキシ)メチル)-4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-(1,1-ジオキシドチオモルホリノ)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)シクロヘキサ-3-エン-1-カルボン酸の調製
4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-(1,1-ジオキシドチオモルホリノ)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)-1-(((1-エチル-1H-1,2,3-トリアゾール-5-イル)オキシ)メチル)シクロヘキサ-3-エン-1-カルボン酸の調製
1H NMR (400MHz, クロロホルム-d) δ 7.10 (s, 1H), 5.36 (br. s., 1H), 5.18 (br. s., 1H), 4.69 (s, 1H), 4.59 (s, 1H), 4.28 - 4.20 (m, 2H), 4.16 (q, J=7.3 Hz, 2H), 3.13 - 2.99 (m, 8H), 2.82 - 2.55 (m, 6H), 2.24 - 1.00 (m, 27H), 1.68 (s, 3H), 1.43 (t, J=7.3 Hz, 3H), 1.09 (s, 3H), 0.98 (s, 3H), 0.96 - 0.91 (m, 6H), 0.85 (s, 3H). LC/MS m/z 820.55 (M+H)+, 2.86分 (LCMS方法3).
1-((ベンゾ[d]イソチアゾール-3-イルオキシ)メチル)-4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-(1,1-ジオキシドチオモルホリノ)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)シクロヘキサ-3-エン-1-カルボン酸の調製
4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-(1,1-ジオキシドチオモルホリノ)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)-1-((ピリジン-4-イルオキシ)メチル)シクロヘキサ-3-エン-1-カルボン酸の調製
4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-(1,1-ジオキシドチオモルホリノ)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)-1-((ピリジン-3-イルオキシ)メチル)シクロヘキサ-3-エンカルボン酸の調製
エチル4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-(1,1-ジオキシドチオモルホリノ)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)-1-((ピリジン-3-イルオキシ)メチル)シクロヘキサ-3-エン-1-カルボキシレートについてはLCMS: m/e 830.50 (M+H)+, 2.363分(LCMS方法8). 1H NMR (400MHz, クロロホルム-d) δ 8.28 (d, J=2.0 Hz, 1H), 8.21 (dd, J=4.0, 2.0 Hz, 1H), 7.23 - 7.16 (m, 2H), 5.35 (br. s., 1H), 5.17 (d, J=4.8 Hz, 1H), 4.72 (d, J=1.8 Hz, 1H), 4.59 (s, 1H), 4.15 - 4.09 (m, 4H), 3.14 - 2.96 (m, 8H), 2.91 - 2.48 (m, 6H), 1.68 (s, 3H), 1.05 (s, 3H), 2.29 - 1.00 (m, 30H), 0.97 - 0.89 (m, 9H), 0.86 - 0.81 (m, 3H).
エチル4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-5a,5b,8,8,11a-ペンタメチル-3a-((2-(4-(メチルスルホニル)ピペリジン-1-イル)エチル)アミノ)-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)-1-((ピリジン-3-イルオキシ)メチル)シクロヘキサ-3-エンカルボキシレートについてはLCMS: m/e 858.55 (M+H)+, 2.454分(LCMS方法8). 1H NMR (400MHz, クロロホルム-d) δ 8.28 (d, J=1.8 Hz, 1H), 8.21 (dd, J=4.0, 1.8 Hz, 1H), 7.20 - 7.16 (m, 2H), 5.35 (br. s., 1H), 5.17 (d, J=4.8 Hz, 1H), 4.72 (d, J=1.8 Hz, 1H), 4.58 (s, 1H), 4.20 - 4.05 (m, 4H), 3.11 (t, J=8.5 Hz, 2H), 2.83 (s, 3H), 2.88-2.76 (m, 1H), 2.2.74 - 2.38 (m, 7H), 1.68 (s, 3H), 1.06 (s, 3H), 2.27 - 0.78 (m, 47H).
4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-5a,5b,8,8,11a-ペンタメチル-3a-((2-(4-(メチルスルホニル)ピペリジン-1-イル)エチル)アミノ)-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)-1-((ピリジン-3-イルオキシ)メチル)シクロヘキサ-3-エンカルボン酸の調製
4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-(1,1-ジオキシドチオモルホリノ)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)-1-(((5-メチルイソチアゾール-3-イル)オキシ)メチル)シクロヘキサ-3-エン-1-カルボン酸の調製
4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-(1,1-ジオキシドチオモルホリノ)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)-1-(((1-メチル-1H-テトラゾール-5-イル)オキシ)メチル)シクロヘキサ-3-エン-1-カルボン酸の調製
4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-(1,1-ジオキシドチオモルホリノ)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)-1-(((5-オキソ-4,5-ジヒドロ-1,2,4-チアジアゾール-3-イル)オキシ)メチル)シクロヘキサ-3-エン-1-カルボン酸の調製
4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-(1,1-ジオキシドチオモルホリノ)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)-1-((チアゾール-2-イルオキシ)メチル)シクロヘキサ-3-エン-1-カルボン酸の調製
4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-(1,1-ジオキシドチオモルホリノ)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)-1-(((1-フェニル-1H-1,2,3-トリアゾール-5-イル)オキシ)メチル)シクロヘキサ-3-エン-1-カルボン酸の調製
4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-(1,1-ジオキシドチオモルホリノ)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)-1-(((1-イソプロピル-1H-1,2,3-トリアゾール-5-イル)オキシ)メチル)シクロヘキサ-3-エン-1-カルボン酸の調製
4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-(1,1-ジオキシドチオモルホリノ)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)-1-(((5-(プロパ-1-エン-2-イル)イソチアゾール-3-イル)オキシ)メチル)シクロヘキサ-3-エン-1-カルボン酸の調製
4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-(1,1-ジオキシドチオモルホリノ)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)-1-((ピリダジン-3-イルオキシ)メチル)シクロヘキサ-3-エン-1-カルボン酸の調製
(R)-4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-(1,1-ジオキシドチオモルホリノ)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)-1-((ピリジン-2-イルオキシ)メチル)シクロヘキサ-3-エン-1-カルボン酸の調製
(R)-4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-(1,1-ジオキシドチオモルホリノ)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)-1-((ピリミジン-4-イルオキシ)メチル)シクロヘキサ-3-エン-1-カルボン酸の調製
(R)-1-(((3-クロロピリジン-2-イル)オキシ)メチル)-4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-(1,1-ジオキシドチオモルホリノ)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)シクロヘキサ-3-エン-1-カルボン酸の調製
(R)-1-(((3-シアノピリジン-2-イル)オキシ)メチル)-4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-(1,1-ジオキシドチオモルホリノ)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)シクロヘキサ-3-エン-1-カルボン酸の調製
(R)-1-(((3-カルバモイルピリジン-2-イル)オキシ)メチル)-4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-(1,1-ジオキシドチオモルホリノ)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)シクロヘキサ-3-エン-1-カルボン酸の調製
(S)-1-(((3-シアノピリジン-2-イル)オキシ)メチル)-4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-(1,1-ジオキシドチオモルホリノ)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)シクロヘキサ-3-エン-1-カルボン酸の調製
国際公開第2015157483号に記載されているようにして調製した(R)-4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-(1,1-ジオキシドチオモルホリノ)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)-1-(フルオロメチル)シクロヘキサ-3-エンカルボン酸(4.08g、5.61mmol)の1,4-ジオキサン(50.0mL)中の懸濁液を含有するフラスコに、水酸化テトラブチルアンモニウム(水中55%)(26.5g、56.1mmol)を加えた。フラスコを還流冷却器に取り付け、油浴中で100℃に加熱した。8.5日加熱した後、LC/MSは反応が完了していることを示した。混合物をrtに冷却し、目盛付き添加漏斗に移した。添加漏斗中に放置したところ、2つの明瞭な層が形成された。生成物を含有する底層を漏斗の目盛に基づいて折半した。物質の半分を1NのHClを加えることによって酸性にした。生成した固体をろ過によって集め、水で洗浄した。その後固体をエーテルと共にすりつぶし、ろ過により集めた。次に固体をエーテルで洗浄し、ろ紙上で乾燥させた。標題生成物を白色の固体(1.95g、2.56mmol、45.6%収率、混合物の半分として計算すると91%)として単離した。LCMS: m/e 725.4 (M+H)+、1.15分(方法16)。
(S)-1-(((3-カルバモイルピリジン-2-イル)オキシ)メチル)-4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-(1,1-ジオキシドチオモルホリノ)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)シクロヘキサ-3-エン-1-カルボン酸の調製
(R)-4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-(1,1-ジオキシドチオモルホリノ)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)-1-(((3-(メトキシカルボニル)ピリジン-2-イル)オキシ)メチル)シクロヘキサ-3-エン-1-カルボン酸の調製
(S)-4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-(1,1-ジオキシドチオモルホリノ)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)-1-(((6-メトキシピリジン-2-イル)オキシ)メチル)シクロヘキサ-3-エン-1-カルボン酸の調製
(S)-4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-(1,1-ジオキシドチオモルホリノ)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)-1-(((6-フルオロピリジン-2-イル)オキシ)メチル)シクロヘキサ-3-エン-1-カルボン酸の調製
(S)-1-(((4-カルバモイルピリジン-2-イル)オキシ)メチル)-4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-(1,1-ジオキシドチオモルホリノ)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)シクロヘキサ-3-エン-1-カルボン酸の調製
(S)-4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-(1,1-ジオキシドチオモルホリノ)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)-1-((ピリジン-2-イルオキシ)メチル)シクロヘキサ-3-エン-1-カルボン酸の調製
(S)-4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-(1,1-ジオキシドチオモルホリノ)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)-1-((ピラジン-2-イルオキシ)メチル)シクロヘキサ-3-エン-1-カルボン酸の調製
4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-(4-ヒドロキシ-1,1-ジオキシドテトラヒドロ-2H-チオピラン-4-イル)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)-1-((ピリジン-2-イルオキシ)メチル)シクロヘキサ-3-エン-1-カルボン酸の調製
4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-(1,1-ジオキシドチオモルホリノ)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)-1-((ピリミジン-2-イルオキシ)メチル)シクロヘキサ-3-エン-1-カルボン酸の調製
4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-(1,1-ジオキシドチオモルホリノ)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)-1-(((7-メトキシイソキノリン-1-イル)オキシ)メチル)シクロヘキサ-3-エン-1-カルボン酸の調製
1-(((3-シアノピリジン-2-イル)オキシ)メチル)-4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-(1,1-ジオキシドチオモルホリノ)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)シクロヘキサ-3-エン-1-カルボン酸の調製
1H NMR (400MHz, クロロホルム-d) δ 7.92 (d, J=7.8 Hz, 2H), 7.65 - 7.54 (m, 1H), 7.44 - 7.37 (m, 2H), 7.35 - 7.27 (m, 5H), 5.25 (s, 2H), 4.46 (s, 2H), 2.63 - 2.35 (m, 6H), 1.86 (td, J=12.4, 5.0 Hz, 2H).
1-(((4-シアノピリジン-2-イル)オキシ)メチル)-4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-(1,1-ジオキシドチオモルホリノ)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)シクロヘキサ-3-エン-1-カルボン酸の調製
1-(((5-シアノピリジン-2-イル)オキシ)メチル)-4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-(1,1-ジオキシドチオモルホリノ)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)シクロヘキサ-3-エン-1-カルボン酸の調製
1-(((6-シアノピリジン-2-イル)オキシ)メチル)-4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-(1,1-ジオキシドチオモルホリノ)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)シクロヘキサ-3-エン-1-カルボン酸の調製
1-(((6-カルバモイルピリジン-2-イル)オキシ)メチル)-4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-(1,1-ジオキシドチオモルホリノ)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)シクロヘキサ-3-エン-1-カルボン酸の調製
1H NMR (400MHz, CDCl3) δ 5.96 - 5.79 (m, 1H), 5.26 - 5.21 (m, 1H), 5.18 (ddt, J=17.1, 2.1, 1.2 Hz, 1H), 2.85 (s, 3H), 2.80 (tt, J=12.5, 3.6 Hz, 1H), 2.25 (d, J=7.5 Hz, 2H), 2.15 - 2.07 (m, 2H), 1.97 (qd, J=13.0, 3.8 Hz, 2H), 1.88 - 1.81 (m, 2H), 1.52 - 1.42 (m, 2H); 13C NMR (100MHz, CDCl3) δ 132.50, 120.02, 69.06, 62.26, 47.86, 36.85, 35.67, 21.13.
(cis)-1-アリル-4-(メチルスルホニル)シクロヘキサノールの構造はX線結晶構造解析で確認した。
1H NMR (400MHz, CDCl3) δ 5.88 (ddt, J=17.2, 10.1, 7.4 Hz, 1H), 5.28 - 5.16 (m, 2H), 2.98 - 2.91 (m, 1H), 2.90 (s, 3H), 2.35 (d, J=7.5 Hz, 2H), 2.23 - 2.14 (m, 2H), 2.02 - 1.93 (m, 2H), 1.90 - 1.78 (m, 2H), 1.57 - 1.46 (m, 2H); 13C NMR (100MHz, CDCl3) δ 132.62, 120.19, 69.20, 62.41, 48.00, 36.98, 35.83, 21.29.
4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-((1s,4R)-1-ヒドロキシ-4-(メチルスルホニル)シクロへキシル)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)-1-((ピリジン-2-イルオキシ)メチル)シクロヘキサ-3-エンカルボン酸の調製
(S)-1-(((3-シアノピリジン-2-イル)オキシ)メチル)-4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-((1s,4R)-1-ヒドロキシ-4-(メチルスルホニル)シクロへキシル)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)シクロヘキサ-3-エンカルボン酸の調製
(S)-1-(((3-シアノピリジン-2-イル)オキシ)メチル)-4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-((1s,4R)-1-ヒドロキシ-4-(メチルスルホニル)シクロへキシル)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)シクロヘキサ-3-エンカルボン酸の調製
(S)-1-(((3-シアノピリジン-2-イル)オキシ)メチル)-4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-((1r,4S)-1-ヒドロキシ-4-(メチルスルホニル)シクロへキシル)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)シクロヘキサ-3-エンカルボン酸の調製
(R)-1-(((3-シアノピリジン-2-イル)オキシ)メチル)-4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-((1s,4R)-1-ヒドロキシ-4-(メチルスルホニル)シクロへキシル)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)シクロヘキサ-3-エンカルボン酸の調製
(R)-1-(((3-シアノピリジン-2-イル)オキシ)メチル)-4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-((1r,4S)-1-ヒドロキシ-4-(メチルスルホニル)シクロへキシル)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)シクロヘキサ-3-エンカルボン酸の調製
(R)-1-(((3-シアノピリジン-2-イル)オキシ)メチル)-4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-(((R)-2,3-ジヒドロキシプロピル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)シクロヘキサ-3-エンカルボン酸TFA(実施例A7)及び(R)-1-(((3-カルバモイルピリジン-2-イル)オキシ)メチル)-4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-(((R)-2,3-ジヒドロキシプロピル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)シクロヘキサ-3-エンカルボン酸(実施例A8)の調製
(R)-1-(((3-シアノピリジン-2-イル)オキシ)メチル)-4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-(((R)-2-ヒドロキシ-3-メトキシプロピル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)シクロヘキサ-3-エンカルボン酸(実施例A9)及び(R)-1-(((3-カルバモイルピリジン-2-イル)オキシ)メチル)-4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-(((R)-2-ヒドロキシ-3-メトキシプロピル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)シクロヘキサ-3-エンカルボン酸(実施例A10)の調製
(R)-1-(((3-シアノピリジン-2-イル)オキシ)メチル)-4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-(((S)-2-ヒドロキシ-3-メトキシプロピル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)シクロヘキサ-3-エンカルボン酸TFA(実施例A11)及び(R)-1-(((3-カルバモイルピリジン-2-イル)オキシ)メチル)-4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-(((S)-2-ヒドロキシ-3-メトキシプロピル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)シクロヘキサ-3-エンカルボン酸TFA(実施例A12)の調製
(R)-1-(((3-シアノピリジン-2-イル)オキシ)メチル)-4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-(((R)-2,3-ジヒドロキシ-2-メチルプロピル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)シクロヘキサ-3-エンカルボン酸TFA(実施例A13)及び(R)-1-(((3-カルバモイルピリジン-2-イル)オキシ)メチル)-4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-(((R)-2,3-ジヒドロキシ-2-メチルプロピル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)シクロヘキサ-3-エンカルボン酸TFA(実施例A14)の調製
(R)-4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-(((R)-2-カルボキシ-2-ヒドロキシエチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)-1-(((3-シアノピリジン-2-イル)オキシ)メチル)シクロヘキサ-3-エンカルボン酸TFA(実施例A15)及び2-(((R)-1-カルボキシ-4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-(((R)-2-カルボキシ-2-ヒドロキシエチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)シクロヘキサ-3-エン-1-イル)メトキシ)ニコチン酸TFA(実施例A16)の調製
(R)-4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-(((S)-2-カルボキシ-2-ヒドロキシエチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)-1-(((3-シアノピリジン-2-イル)オキシ)メチル)シクロヘキサ-3-エンカルボン酸TFA(実施例A17)及び(R)-3-(((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-9-((S)-4-(((3-カルバモイルピリジン-2-イル)オキシ)メチル)-4-(エトキシカルボニル)シクロヘキサ-1-エン-1-イル)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-3a-イル)アミノ)-2-ヒドロキシプロパン酸TFA(実施例A18)の調製
(1R)-4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-カルボキシ-2-ヒドロキシプロピル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)-1-(((3-シアノピリジン-2-イル)オキシ)メチル)シクロヘキサ-3-エンカルボン酸の調製
4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-(1,1-ジオキシドチオモルホリノ)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)-1-(2-(ピリジン-2-イルオキシ)エチル)シクロヘキサ-3-エン-1-カルボン酸の調製
4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-(1,1-ジオキシドチオモルホリノ)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)-1-(2-((5-メチルイソチアゾール-3-イル)オキシ)エチル)シクロヘキサ-3-エン-1-カルボン酸の調製
2-(2-(1-カルボキシ-4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-(1,1-ジオキシドチオモルホリノ)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)シクロヘキサ-3-エン-1-イル)エトキシ)イソニコチン酸の調製
1-(2-((4-シアノピリジン-2-イル)オキシ)エチル)-4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-(1,1-ジオキシドチオモルホリノ)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)シクロヘキサ-3-エン-1-カルボン酸の調製
4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-(1,1-ジオキシドチオモルホリノ)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)-1-(2-(ピリミジン-2-イルオキシ)エチル)シクロヘキサ-3-エン-1-カルボン酸の調製
4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-(1,1-ジオキシドチオモルホリノ)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)-1-(2-((4-メチルピリミジン-2-イル)オキシ)エチル)シクロヘキサ-3-エン-1-カルボン酸の調製
4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-(1,1-ジオキシドチオモルホリノ)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)-1-(2-((4-メトキシピリミジン-2-イル)オキシ)エチル)シクロヘキサ-3-エン-1-カルボン酸の調製
4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-(1,1-ジオキシドチオモルホリノ)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)-1-(2-((3-メチルピリジン-2-イル)オキシ)エチル)シクロヘキサ-3-エン-1-カルボン酸の調製
1-(2-((3-クロロピリジン-2-イル)オキシ)エチル)-4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-(1,1-ジオキシドチオモルホリノ)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)シクロヘキサ-3-エン-1-カルボン酸の調製
4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-(1,1-ジオキシドチオモルホリノ)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)-1-(2-((3-(トリフルオロメチル)ピリジン-2-イル)オキシ)エチル)シクロヘキサ-3-エン-1-カルボン酸の調製
4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-(1,1-ジオキシドチオモルホリノ)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)-1-(2-(ピラジン-2-イルオキシ)エチル)シクロヘキサ-3-エン-1-カルボン酸の調製
4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-(1,1-ジオキシドチオモルホリノ)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)-1-(2-((4-メトキシピリジン-2-イル)オキシ)エチル)シクロヘキサ-3-エン-1-カルボン酸の調製
1-(2-((4-ブロモピリジン-2-イル)オキシ)エチル)-4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-(1,1-ジオキシドチオモルホリノ)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)シクロヘキサ-3-エン-1-カルボン酸の調製
1-(2-((4-クロロピリジン-2-イル)オキシ)エチル)-4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-(1,1-ジオキシドチオモルホリノ)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)シクロヘキサ-3-エン-1-カルボン酸の調製
1-(2-((2-クロロピリジン-4-イル)オキシ)エチル)-4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((2-(1,1-ジオキシドチオモルホリノ)エチル)アミノ)-5a,5b,8,8,11a-ペンタメチル-1-(プロパ-1-エン-2-イル)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-オクタデカヒドロ-1H-シクロペンタ[a]クリセン-9-イル)シクロヘキサ-3-エン-1-カルボン酸の調製
細胞 MT-2細胞及び293T細胞はNIH AIDS Research and Reference Reagent Programから入手した。細胞株を、10%加熱不活性化ウシ胎児血清(FBS)、100単位/mLのペニシリンG及び100μg/mLのストレプトマイシンを補充したRPMI 1640(MT-2)又はDMEM(293T、HeLa)培地で週二回継代培養した。DMEM培地はさらに10mM HEPESバッファー、pH 7.55、2mM L-グルタミン及び0.25μg/mLのアムホテリシンBを補充した。
ウミシイタケルシフェラーゼ遺伝子を発現するHIV-1 NL4-3を部位特異的突然変異誘発によりgag V370A/ΔT371ウイルスに転換した。A364Vは部位特異的突然変異体である。
ii Dierynck, I, Van Markck, H, Van Ginderen, M, Jonckers, TH, Nalam, MN, Schiffer, CA, Raoof, A, Kraus, G, Picchio, G. TMC310911, a novel human immunodeficiency virus type 1 protease inhibitor, shows in vitro an improved resistance profile and higher genetic barrier to resistance compared
iii Stray KM, Callebaut C, Glass B, Tsai L, Xu L, Muller B, Krausslich HG, Cihlar T. Mutations in multiple domains of Gag drive the emergence of in vitor resistance to the phosphonate-containing HIV-1 protease inhibitor GS-8374. J Virol. 2013 87:454-63
本発明の実施形態として例えば以下を挙げることができる。
[実施形態1]
薬学的に許容されるその塩を含む、式Iの化合物
Aは、-C 1〜6 アルキル-OR 0 であり、
ここでR 0 はヘテロアリール-Q 0 であり、
Q 0 は、-H、-CN、-C 1〜6 アルキル、-COOH、-Ph、-OC 1〜6 アルキル、-ハロ、-CF 3 の群から選択され、
Yは、-COOR 2 、-C(O)NR 2 SO 2 R 3 、-C(O)NHSO 2 NR 2 R 2 、-SO 2 NR 2 C(O)R 2 、-テトラゾール、及び-CONHOHの群から選択され、
ここで、n=1〜6であり、
R 2 は、-H、-C 1〜6 アルキル、-アルキル置換C 1〜6 アルキル又は-アリール置換C 1〜6 アルキルであり、
Wは、不在であるか、又は-CH 2 -若しくは-CO-であり、
R 3 は、-H、-C 1〜6 アルキル又は-アルキル置換C 1〜6 アルキルであり、
R 4 は、-H、-C 1〜6 アルキル、-C 1〜6 アルキル-C 3〜6 シクロアルキル、-C 1〜6 置換-C 1〜6 アルキル、-C 1〜6 アルキル-Q 1 、-C 1〜6 アルキル-C 3〜6 シクロアルキル-Q 1 、アリール、ヘテロアリール、置換ヘテロアリール、-COR 6 、-SO 2 R 7 、-SO 2 NR 2 R 2 、及び
ここでGは、-O-、-SO 2 -及び-NR 12 -の群から選択され、
ここでQ 1 は、-C 1〜6 アルキル、-C 1〜6 フルオロアルキル、ヘテロアリール、置換ヘテロアリール、ハロゲン、-CF 3 、-OR 2 、-COOR 2 、-NR 8 R 9、 -CONR 8 R 9 及び-SO 2 R 7 の群から選択され、
R 5 は、-H、-C 1〜6 アルキル、-C 3〜6 シクロアルキル、-C 1〜6 アルキル置換アルキル、-C 1〜6 アルキル-NR 8 R 9、 -COR 3 、-SO 2 R 7 及び-SO 2 NR 2 R 2 の群から選択され、
但し、R 4 又はR 5 は、Wが-CO-である場合、-COR 6 ではないことが条件であり、
さらに、R 4 又はR 5 の一方のみが、-COR 6 、-COCOR 6 ,-SO 2 R 7 及び-SO 2 NR 2 R 2 の群から選択されることが条件であり、
R 6 は-H、-C 1〜6 アルキル、-C 1〜6 アルキル置換アルキル、-C 3〜6 シクロアルキル、-C 3〜6 置換シクロアルキル-Q 2 、-C 1〜6 アルキル-Q 2 、-C 1〜6 アルキル置換アルキル-Q 2 、-C 3〜6 シクロアルキル-Q 2 、アリール-Q 2 、-NR 13 R 14 、及び-OR 15 の群から選択され、
ここでQ 2 はアリール、ヘテロアリール、置換ヘテロアリール、-OR 2 、-COOR 2 、-NR 8 R 9 、SO 2 R 7 、-CONHSO 2 R 3 、及び-CONHSO 2 NR 2 R 2 の群から選択され、
R 7 は-H、-C 1〜6 アルキル、-C 1〜6 置換アルキル、-C 3〜6 シクロアルキル、-CF 3 、アリール、及びヘテロアリールの群から選択され、
R 8 及びR 9 は、-H、-C 1〜6 アルキル、-C 1〜6 置換アルキル、アリール、ヘテロアリール、置換アリール、置換ヘテロアリール、-C 1〜6 アルキル-Q 2 、及び-COOR 3 の群から独立して選択され、
又はR 8 及びR 9 は、隣接するNと一緒になって
Mは、-R 15 、-SO 2 R 2 、-SO 2 NR 2 R 2 、-OH及び-NR 2 R 12 の群から選択され、
Vは、-CR 10 R 11 -、-SO 2 -、-O-及び-NR 12 -の群から選択され、
但し、R 8 又はR 9 の一方のみが-COOR 3 であり得ることが条件であり、
R 10 及びR 11 は、-H、-C 1〜6 アルキル、-C 1〜6 置換アルキル及び-C 3〜6 シクロアルキルの群から独立して選択され、
R 12 は、-H、-C 1〜6 アルキル、-アルキル置換C 1〜6 アルキル、-CONR 2 R 2 、-SO 2 R 3 、及び-SO 2 NR 2 R 2 の群から選択され、
R 13 及びR 14 は、-H、-C 1〜6 アルキル、-C 3〜6 シクロアルキル、-C 1〜6 置換アルキル、-C 1〜6 アルキル-Q 3 、-C 1〜6 アルキル-C 3〜6 シクロアルキル-Q 3 、及びC 1〜6 置換アルキル-Q 3 の群から独立して選択され、
Q 3 は、ヘテロアリール、置換ヘテロアリール、-NR 2 R 12 、-CONR 2 R 2 、-COOR 2 、-OR 2 、及び-SO 2 R 3 の群から選択され、
R 15 は、-C 1〜6 アルキル、-C 3〜6 シクロアルキル、-C 1〜6 置換アルキル、-C 1〜6 アルキル-Q 3 、-C 1〜6 アルキル-C 3〜6 シクロアルキル-Q 3 及び-C 1〜6 置換アルキル-Q 3 の群から選択され、
R 16 は、-H、-C 1〜6 アルキル、-NR 2 R 2 、及び-COOR 2 の群から選択され、
但し、Vが-NR 12 -である場合、R 16 は-NR 2 R 2 でないことが条件であり、
R 17 は、-H、-C 1〜6 アルキル、-COOR 3 、及びアリールの群から選択される]。
[実施形態2]
R 0 基のヘテロアリール部分が
[実施形態3]
R 1 がイソプロぺニルである、実施形態2に記載の化合物。
[実施形態4]
Yが-COOR 2 である、実施形態3に記載の化合物。
[実施形態5]
R 2 が-Hである、実施形態4に記載の化合物。
[実施形態6]
R 4 が-C 1〜6 アルキル-Q 1 である、実施形態1に記載の化合物。
[実施形態7]
Q 1 が-NR 8 R 9 である、実施形態6に記載の化合物。
[実施形態8]
R 8 及びR 9 が隣接する-Nと一緒になって環を形成する場合、環が
[実施形態9]
R 7 及びR 16 が各々-H及び-C 1〜6 アルキルの群から選択される、実施形態8に記載の化合物。
[実施形態10]
Q 0 が-CNである、実施形態1に記載の化合物。
[実施形態11]
R 1 がイソプロぺニルであり、R 0 基の「ヘテロアリール」部分が
[実施形態12]
[実施形態13]
[実施形態14]
HIVを寛解させる量の1つ以上の実施形態1に記載の化合物を、1つ以上の薬学的に許容される担体、賦形剤、及び/又は希釈剤と一緒に含む組成物。
[実施形態15]
HIVを寛解させる量の1つ以上の実施形態11に記載の化合物を、1つ以上の薬学的に許容される担体、賦形剤、及び/又は希釈剤と一緒に含む組成物。
[実施形態16]
HIVを寛解させる量の1つ以上の実施形態12に記載の化合物を、1つ以上の薬学的に許容される担体、賦形剤、及び/又は希釈剤と一緒に含む組成物。
[実施形態17]
HIVを寛解させる量の1つ以上の実施形態13に記載の化合物を、1つ以上の薬学的に許容される担体、賦形剤、及び/又は希釈剤と一緒に含む組成物。
[実施形態18]
HIVウイルスに感染した哺乳動物を治療する方法であって、HIVを寛解させる量の実施形態1に記載の化合物を1つ以上の薬学的に許容される担体、賦形剤、及び/又は希釈剤と一緒に前記哺乳動物に投与することを含む、方法。
[実施形態19]
HIVウイルスに感染した哺乳動物を治療する方法であって、HIVを寛解させる量の実施形態12に記載の化合物を1つ以上の薬学的に許容される担体、賦形剤、及び/又は希釈剤と一緒に前記哺乳動物に投与することを含む、方法。
[実施形態20]
HIVウイルスに感染した哺乳動物を治療する方法であって、HIVを寛解させる量の実施形態13に記載の化合物を1つ以上の薬学的に許容される担体、賦形剤、及び/又は希釈剤と一緒に前記哺乳動物に投与することを含む、方法。
[実施形態21]
T332S/V362I/pr R41Gとして同定される三重突然変異タンパク質。
Claims (7)
- 以下:
- 以下:
- 以下:
- 以下:
- 以下:
- 請求項1〜5のいずれか1項に記載の化合物又は塩を含む医薬組成物。
- 請求項1〜5のいずれか1項に記載の化合物又は塩を含む、HIVウイルスに感染した哺乳動物を治療するための医薬組成物。
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