JP2007533741A - Bace阻害剤 - Google Patents
Bace阻害剤 Download PDFInfo
- Publication number
- JP2007533741A JP2007533741A JP2007509508A JP2007509508A JP2007533741A JP 2007533741 A JP2007533741 A JP 2007533741A JP 2007509508 A JP2007509508 A JP 2007509508A JP 2007509508 A JP2007509508 A JP 2007509508A JP 2007533741 A JP2007533741 A JP 2007533741A
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- JP
- Japan
- Prior art keywords
- alkyl
- mmol
- hydrogen
- methyl
- cycloalkyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Ceased
Links
- 229940126077 BACE inhibitor Drugs 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims abstract description 311
- 102100021257 Beta-secretase 1 Human genes 0.000 claims abstract description 10
- 101000894895 Homo sapiens Beta-secretase 1 Proteins 0.000 claims abstract description 8
- -1 hydroxy, p-toluenesulfonyloxy Chemical group 0.000 claims description 334
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims description 302
- 229910052739 hydrogen Inorganic materials 0.000 claims description 161
- 239000001257 hydrogen Chemical group 0.000 claims description 161
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 123
- 229910052757 nitrogen Inorganic materials 0.000 claims description 107
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 102
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 95
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 93
- 125000001153 fluoro group Chemical group F* 0.000 claims description 90
- SNOOUWRIMMFWNE-UHFFFAOYSA-M sodium;6-[(3,4,5-trimethoxybenzoyl)amino]hexanoate Chemical compound [Na+].COC1=CC(C(=O)NCCCCCC([O-])=O)=CC(OC)=C1OC SNOOUWRIMMFWNE-UHFFFAOYSA-M 0.000 claims description 74
- 150000002431 hydrogen Chemical group 0.000 claims description 73
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 68
- 125000005843 halogen group Chemical group 0.000 claims description 60
- 125000000217 alkyl group Chemical group 0.000 claims description 52
- 125000001424 substituent group Chemical group 0.000 claims description 42
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 41
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 claims description 30
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 29
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 25
- RWRIWBAIICGTTQ-UHFFFAOYSA-N difluoromethane Chemical compound FCF RWRIWBAIICGTTQ-UHFFFAOYSA-N 0.000 claims description 24
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 24
- 150000003839 salts Chemical class 0.000 claims description 24
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 claims description 23
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 21
- 208000024827 Alzheimer disease Diseases 0.000 claims description 20
- NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical compound ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 claims description 20
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 20
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims description 18
- 239000002253 acid Substances 0.000 claims description 18
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims description 17
- 125000005073 adamantyl group Chemical group C12(CC3CC(CC(C1)C3)C2)* 0.000 claims description 16
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical group C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims description 14
- 125000002541 furyl group Chemical group 0.000 claims description 14
- 238000004519 manufacturing process Methods 0.000 claims description 14
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 14
- 125000004076 pyridyl group Chemical group 0.000 claims description 14
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 12
- 229910052799 carbon Inorganic materials 0.000 claims description 12
- 125000003386 piperidinyl group Chemical group 0.000 claims description 12
- 101800001718 Amyloid-beta protein Proteins 0.000 claims description 11
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims description 11
- 239000003814 drug Substances 0.000 claims description 11
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims description 10
- 125000000000 cycloalkoxy group Chemical group 0.000 claims description 10
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 10
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 9
- 208000010877 cognitive disease Diseases 0.000 claims description 9
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 9
- 208000027061 mild cognitive impairment Diseases 0.000 claims description 9
- 150000003573 thiols Chemical class 0.000 claims description 9
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical group C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims description 8
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 claims description 8
- ZSIQJIWKELUFRJ-UHFFFAOYSA-N azepane Chemical group C1CCCNCC1 ZSIQJIWKELUFRJ-UHFFFAOYSA-N 0.000 claims description 8
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 8
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 claims description 8
- 230000005764 inhibitory process Effects 0.000 claims description 8
- 239000008194 pharmaceutical composition Substances 0.000 claims description 8
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 claims description 7
- 125000004504 1,2,4-oxadiazolyl group Chemical group 0.000 claims description 7
- 125000004214 1-pyrrolidinyl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 claims description 7
- 239000004305 biphenyl Chemical group 0.000 claims description 7
- 235000010290 biphenyl Nutrition 0.000 claims description 7
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 claims description 7
- 201000010099 disease Diseases 0.000 claims description 7
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 claims description 7
- 230000002401 inhibitory effect Effects 0.000 claims description 7
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 7
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 7
- 125000002971 oxazolyl group Chemical group 0.000 claims description 7
- 125000000587 piperidin-1-yl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims description 7
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 claims description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 5
- 125000000335 thiazolyl group Chemical group 0.000 claims description 5
- 239000003085 diluting agent Substances 0.000 claims description 4
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 4
- 125000000719 pyrrolidinyl group Chemical group 0.000 claims description 4
- 208000024891 symptom Diseases 0.000 claims description 4
- 125000004299 tetrazol-5-yl group Chemical group [H]N1N=NC(*)=N1 0.000 claims description 4
- 230000001668 ameliorated effect Effects 0.000 claims description 2
- 125000003943 azolyl group Chemical group 0.000 claims description 2
- 239000003937 drug carrier Substances 0.000 claims description 2
- 238000002360 preparation method Methods 0.000 abstract description 97
- 239000000543 intermediate Substances 0.000 abstract description 16
- 238000000034 method Methods 0.000 abstract description 15
- 239000003112 inhibitor Substances 0.000 abstract description 12
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 615
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 256
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 228
- 239000012141 concentrate Substances 0.000 description 206
- 235000008504 concentrate Nutrition 0.000 description 206
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 180
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 172
- 239000000243 solution Substances 0.000 description 167
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 162
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 146
- 238000003756 stirring Methods 0.000 description 132
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 126
- 229920006395 saturated elastomer Polymers 0.000 description 125
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 114
- 235000019341 magnesium sulphate Nutrition 0.000 description 114
- 238000010898 silica gel chromatography Methods 0.000 description 107
- 239000000203 mixture Substances 0.000 description 103
- 239000000284 extract Substances 0.000 description 97
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 89
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 89
- 239000011780 sodium chloride Substances 0.000 description 86
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 73
- 238000006243 chemical reaction Methods 0.000 description 58
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 56
- 239000003795 chemical substances by application Substances 0.000 description 56
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 53
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical class [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 48
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 46
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 46
- 238000001914 filtration Methods 0.000 description 45
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 44
- 239000010410 layer Substances 0.000 description 43
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 37
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 36
- 239000007787 solid Substances 0.000 description 36
- 239000012044 organic layer Substances 0.000 description 34
- 239000000706 filtrate Substances 0.000 description 29
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 27
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 26
- YJVFFLUZDVXJQI-UHFFFAOYSA-L palladium(ii) acetate Chemical compound [Pd+2].CC([O-])=O.CC([O-])=O YJVFFLUZDVXJQI-UHFFFAOYSA-L 0.000 description 26
- 239000003921 oil Substances 0.000 description 25
- 235000019198 oils Nutrition 0.000 description 25
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 24
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 24
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 22
- 238000005192 partition Methods 0.000 description 22
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 21
- FJDQFPXHSGXQBY-UHFFFAOYSA-L caesium carbonate Chemical compound [Cs+].[Cs+].[O-]C([O-])=O FJDQFPXHSGXQBY-UHFFFAOYSA-L 0.000 description 21
- 229910000024 caesium carbonate Inorganic materials 0.000 description 21
- 235000017557 sodium bicarbonate Nutrition 0.000 description 21
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 21
- 239000011541 reaction mixture Substances 0.000 description 17
- MUALRAIOVNYAIW-UHFFFAOYSA-N binap Chemical group C1=CC=CC=C1P(C=1C(=C2C=CC=CC2=CC=1)C=1C2=CC=CC=C2C=CC=1P(C=1C=CC=CC=1)C=1C=CC=CC=1)C1=CC=CC=C1 MUALRAIOVNYAIW-UHFFFAOYSA-N 0.000 description 16
- BHRZNVHARXXAHW-BYPYZUCNSA-N (2s)-butan-2-amine Chemical compound CC[C@H](C)N BHRZNVHARXXAHW-BYPYZUCNSA-N 0.000 description 15
- 238000010791 quenching Methods 0.000 description 15
- 230000002829 reductive effect Effects 0.000 description 15
- 239000000725 suspension Substances 0.000 description 15
- JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-Diisopropylethylamine (DIPEA) Chemical compound CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 description 14
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 14
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 14
- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 14
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 14
- CYPYTURSJDMMMP-WVCUSYJESA-N (1e,4e)-1,5-diphenylpenta-1,4-dien-3-one;palladium Chemical compound [Pd].[Pd].C=1C=CC=CC=1\C=C\C(=O)\C=C\C1=CC=CC=C1.C=1C=CC=CC=1\C=C\C(=O)\C=C\C1=CC=CC=C1.C=1C=CC=CC=1\C=C\C(=O)\C=C\C1=CC=CC=C1 CYPYTURSJDMMMP-WVCUSYJESA-N 0.000 description 13
- 229960000583 acetic acid Drugs 0.000 description 13
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 description 12
- QMMFVYPAHWMCMS-UHFFFAOYSA-N Dimethyl sulfide Chemical compound CSC QMMFVYPAHWMCMS-UHFFFAOYSA-N 0.000 description 12
- 241000124008 Mammalia Species 0.000 description 12
- 150000001412 amines Chemical class 0.000 description 12
- 235000019270 ammonium chloride Nutrition 0.000 description 12
- 239000012298 atmosphere Substances 0.000 description 12
- 229910000104 sodium hydride Inorganic materials 0.000 description 12
- 125000006288 3,5-difluorobenzyl group Chemical group [H]C1=C(F)C([H])=C(C([H])=C1F)C([H])([H])* 0.000 description 11
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 11
- 238000000746 purification Methods 0.000 description 11
- 238000010992 reflux Methods 0.000 description 11
- 239000012312 sodium hydride Substances 0.000 description 11
- 239000002904 solvent Substances 0.000 description 11
- FPQQSJJWHUJYPU-UHFFFAOYSA-N 3-(dimethylamino)propyliminomethylidene-ethylazanium;chloride Chemical compound Cl.CCN=C=NCCCN(C)C FPQQSJJWHUJYPU-UHFFFAOYSA-N 0.000 description 10
- 125000006284 3-fluorobenzyl group Chemical group [H]C1=C([H])C(=C([H])C(F)=C1[H])C([H])([H])* 0.000 description 10
- 238000007792 addition Methods 0.000 description 10
- 150000001299 aldehydes Chemical class 0.000 description 10
- 239000002480 mineral oil Substances 0.000 description 10
- 235000010446 mineral oil Nutrition 0.000 description 10
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 10
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 9
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 9
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 9
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 9
- 239000006260 foam Substances 0.000 description 9
- LXNAVEXFUKBNMK-UHFFFAOYSA-N palladium(II) acetate Substances [Pd].CC(O)=O.CC(O)=O LXNAVEXFUKBNMK-UHFFFAOYSA-N 0.000 description 9
- 239000002244 precipitate Substances 0.000 description 9
- 239000000741 silica gel Substances 0.000 description 9
- 229910002027 silica gel Inorganic materials 0.000 description 9
- 229910052938 sodium sulfate Inorganic materials 0.000 description 9
- 235000011152 sodium sulphate Nutrition 0.000 description 9
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 9
- 125000005931 tert-butyloxycarbonyl group Chemical group [H]C([H])([H])C(OC(*)=O)(C([H])([H])[H])C([H])([H])[H] 0.000 description 9
- 239000012230 colorless oil Substances 0.000 description 8
- 229910001873 dinitrogen Inorganic materials 0.000 description 8
- 238000002156 mixing Methods 0.000 description 8
- GVWISOJSERXQBM-UHFFFAOYSA-N n-methylpropan-1-amine Chemical compound CCCNC GVWISOJSERXQBM-UHFFFAOYSA-N 0.000 description 8
- 239000011734 sodium Substances 0.000 description 8
- 101710137189 Amyloid-beta A4 protein Proteins 0.000 description 7
- 101710151993 Amyloid-beta precursor protein Proteins 0.000 description 7
- 102100022704 Amyloid-beta precursor protein Human genes 0.000 description 7
- DZHSAHHDTRWUTF-SIQRNXPUSA-N amyloid-beta polypeptide 42 Chemical compound C([C@@H](C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@H](C(=O)NCC(=O)N[C@@H](CO)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCCN)C(=O)NCC(=O)N[C@@H](C)C(=O)N[C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)NCC(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](C(C)C)C(=O)NCC(=O)NCC(=O)N[C@@H](C(C)C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](C)C(O)=O)[C@@H](C)CC)C(C)C)NC(=O)[C@H](CC=1C=CC=CC=1)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CC=1N=CNC=1)NC(=O)[C@H](CC=1N=CNC=1)NC(=O)[C@@H](NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CC=1C=CC(O)=CC=1)NC(=O)CNC(=O)[C@H](CO)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC=1N=CNC=1)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CC=1C=CC=CC=1)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](C)NC(=O)[C@@H](N)CC(O)=O)C(C)C)C(C)C)C1=CC=CC=C1 DZHSAHHDTRWUTF-SIQRNXPUSA-N 0.000 description 7
- 239000006185 dispersion Substances 0.000 description 7
- 229910000027 potassium carbonate Inorganic materials 0.000 description 7
- 238000003786 synthesis reaction Methods 0.000 description 7
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 7
- 108010043324 Amyloid Precursor Protein Secretases Proteins 0.000 description 6
- 102000002659 Amyloid Precursor Protein Secretases Human genes 0.000 description 6
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 6
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 6
- 150000002148 esters Chemical class 0.000 description 6
- KWGKDLIKAYFUFQ-UHFFFAOYSA-M lithium chloride Chemical compound [Li+].[Cl-] KWGKDLIKAYFUFQ-UHFFFAOYSA-M 0.000 description 6
- ASOKPJOREAFHNY-UHFFFAOYSA-N 1-Hydroxybenzotriazole Chemical compound C1=CC=C2N(O)N=NC2=C1 ASOKPJOREAFHNY-UHFFFAOYSA-N 0.000 description 5
- 125000004211 3,5-difluorophenyl group Chemical group [H]C1=C(F)C([H])=C(*)C([H])=C1F 0.000 description 5
- NHQDETIJWKXCTC-UHFFFAOYSA-N 3-chloroperbenzoic acid Chemical compound OOC(=O)C1=CC=CC(Cl)=C1 NHQDETIJWKXCTC-UHFFFAOYSA-N 0.000 description 5
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- KTWOOEGAPBSYNW-UHFFFAOYSA-N ferrocene Chemical compound [Fe+2].C=1C=C[CH-]C=1.C=1C=C[CH-]C=1 KTWOOEGAPBSYNW-UHFFFAOYSA-N 0.000 description 1
- 239000012065 filter cake Substances 0.000 description 1
- VGGRCVDNFAQIKO-UHFFFAOYSA-N formic anhydride Chemical compound O=COC=O VGGRCVDNFAQIKO-UHFFFAOYSA-N 0.000 description 1
- 238000004508 fractional distillation Methods 0.000 description 1
- 229940093915 gynecological organic acid Drugs 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 125000005462 imide group Chemical group 0.000 description 1
- 150000002466 imines Chemical group 0.000 description 1
- 125000002346 iodo group Chemical group I* 0.000 description 1
- HVTICUPFWKNHNG-UHFFFAOYSA-N iodoethane Chemical compound CCI HVTICUPFWKNHNG-UHFFFAOYSA-N 0.000 description 1
- 239000003456 ion exchange resin Substances 0.000 description 1
- 229920003303 ion-exchange polymer Polymers 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
- 125000005929 isobutyloxycarbonyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])OC(*)=O 0.000 description 1
- 150000003951 lactams Chemical class 0.000 description 1
- WGJJZRVGLPOKQT-UHFFFAOYSA-K lanthanum(3+);trifluoromethanesulfonate Chemical compound [La+3].[O-]S(=O)(=O)C(F)(F)F.[O-]S(=O)(=O)C(F)(F)F.[O-]S(=O)(=O)C(F)(F)F WGJJZRVGLPOKQT-UHFFFAOYSA-K 0.000 description 1
- JNODQFNWMXFMEV-UHFFFAOYSA-N latrepirdine Chemical compound C1N(C)CCC2=C1C1=CC(C)=CC=C1N2CCC1=CC=C(C)N=C1 JNODQFNWMXFMEV-UHFFFAOYSA-N 0.000 description 1
- 210000004558 lewy body Anatomy 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004895 liquid chromatography mass spectrometry Methods 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- VFZXMEQGIIWBFJ-UHFFFAOYSA-M magnesium;cyclopropane;bromide Chemical compound [Mg+2].[Br-].C1C[CH-]1 VFZXMEQGIIWBFJ-UHFFFAOYSA-M 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- QARBMVPHQWIHKH-UHFFFAOYSA-N methanesulfonyl chloride Chemical compound CS(Cl)(=O)=O QARBMVPHQWIHKH-UHFFFAOYSA-N 0.000 description 1
- KJGLZJQPMKQFIK-UHFFFAOYSA-N methanolate;tributylstannanylium Chemical compound CCCC[Sn](CCCC)(CCCC)OC KJGLZJQPMKQFIK-UHFFFAOYSA-N 0.000 description 1
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 description 1
- KLGSHNXEUZOKHH-TYSVMGFPSA-N methyl (2r,4r)-4-hydroxypyrrolidine-2-carboxylate;hydrochloride Chemical compound Cl.COC(=O)[C@H]1C[C@@H](O)CN1 KLGSHNXEUZOKHH-TYSVMGFPSA-N 0.000 description 1
- KLGSHNXEUZOKHH-UYXJWNHNSA-N methyl (2r,4s)-4-hydroxypyrrolidine-2-carboxylate;hydrochloride Chemical compound Cl.COC(=O)[C@H]1C[C@H](O)CN1 KLGSHNXEUZOKHH-UYXJWNHNSA-N 0.000 description 1
- JGATXHYMBWIQDB-UHFFFAOYSA-N methyl 2-(benzenesulfonyl)-6-chloropyridine-4-carboxylate Chemical compound COC(=O)C1=CC(Cl)=NC(S(=O)(=O)C=2C=CC=CC=2)=C1 JGATXHYMBWIQDB-UHFFFAOYSA-N 0.000 description 1
- DSBRESWMTUWFNW-IEOXRBHFSA-N methyl 2-(butan-2-ylamino)-6-[(s)-propylsulfinyl]pyridine-4-carboxylate Chemical compound CCC[S@](=O)C1=CC(C(=O)OC)=CC(NC(C)CC)=N1 DSBRESWMTUWFNW-IEOXRBHFSA-N 0.000 description 1
- XZDQEUFNVBDFLY-UHFFFAOYSA-N methyl 2-(butan-2-ylamino)-6-methylsulfonyloxypyridine-4-carboxylate Chemical compound CCC(C)NC1=CC(C(=O)OC)=CC(OS(C)(=O)=O)=N1 XZDQEUFNVBDFLY-UHFFFAOYSA-N 0.000 description 1
- SUJVOSKRBYNLRZ-UHFFFAOYSA-N methyl 2-(butan-2-ylamino)-6-propylsulfanylpyridine-4-carboxylate Chemical compound CCCSC1=CC(C(=O)OC)=CC(NC(C)CC)=N1 SUJVOSKRBYNLRZ-UHFFFAOYSA-N 0.000 description 1
- RNUVOFDVOBVKGK-UHFFFAOYSA-N methyl 2-(cyclobutylamino)-6-methylsulfonylpyridine-4-carboxylate Chemical compound CS(=O)(=O)C1=CC(C(=O)OC)=CC(NC2CCC2)=N1 RNUVOFDVOBVKGK-UHFFFAOYSA-N 0.000 description 1
- UXRFVPDFDJBNDX-UHFFFAOYSA-N methyl 2-(cyclopropylamino)-6-[methyl(methylsulfonyl)amino]pyridine-4-carboxylate Chemical compound CS(=O)(=O)N(C)C1=CC(C(=O)OC)=CC(NC2CC2)=N1 UXRFVPDFDJBNDX-UHFFFAOYSA-N 0.000 description 1
- OWBXWDOOUFOQKR-QMMMGPOBSA-N methyl 2-[[(2s)-butan-2-yl]amino]-6-(1,1-difluoroethyl)pyridine-4-carboxylate Chemical compound CC[C@H](C)NC1=CC(C(=O)OC)=CC(C(C)(F)F)=N1 OWBXWDOOUFOQKR-QMMMGPOBSA-N 0.000 description 1
- CEOPSCNDTNEDRN-JTQLQIEISA-N methyl 2-[[(2s)-butan-2-yl]amino]-6-(1,3-dioxan-2-yl)pyridine-4-carboxylate Chemical compound CC[C@H](C)NC1=CC(C(=O)OC)=CC(C2OCCCO2)=N1 CEOPSCNDTNEDRN-JTQLQIEISA-N 0.000 description 1
- UHRYKGDMRCOFAU-VIFPVBQESA-N methyl 2-[[(2s)-butan-2-yl]amino]-6-(1-ethyltetrazol-5-yl)pyridine-4-carboxylate Chemical compound CC[C@H](C)NC1=CC(C(=O)OC)=CC(C=2N(N=NN=2)CC)=N1 UHRYKGDMRCOFAU-VIFPVBQESA-N 0.000 description 1
- PACUYYVQMKVEOS-VIFPVBQESA-N methyl 2-[[(2s)-butan-2-yl]amino]-6-(2,2-difluoropropyl)pyridine-4-carboxylate Chemical compound CC[C@H](C)NC1=CC(C(=O)OC)=CC(CC(C)(F)F)=N1 PACUYYVQMKVEOS-VIFPVBQESA-N 0.000 description 1
- JHQVWZFGXULXDJ-QMMMGPOBSA-N methyl 2-[[(2s)-butan-2-yl]amino]-6-(2-methyltetrazol-5-yl)pyridine-4-carboxylate Chemical compound CC[C@H](C)NC1=CC(C(=O)OC)=CC(C2=NN(C)N=N2)=N1 JHQVWZFGXULXDJ-QMMMGPOBSA-N 0.000 description 1
- KAPMTHVNQRKTRU-VIFPVBQESA-N methyl 2-[[(2s)-butan-2-yl]amino]-6-(2-oxopropyl)pyridine-4-carboxylate Chemical compound CC[C@H](C)NC1=CC(C(=O)OC)=CC(CC(C)=O)=N1 KAPMTHVNQRKTRU-VIFPVBQESA-N 0.000 description 1
- PCSAAVNJVHLPAF-VIFPVBQESA-N methyl 2-[[(2s)-butan-2-yl]amino]-6-(dimethylsulfamoyl)pyridine-4-carboxylate Chemical compound CC[C@H](C)NC1=CC(C(=O)OC)=CC(S(=O)(=O)N(C)C)=N1 PCSAAVNJVHLPAF-VIFPVBQESA-N 0.000 description 1
- LLVDUWSQFJROBX-JTQLQIEISA-N methyl 2-[[(2s)-butan-2-yl]amino]-6-[cyclopropylsulfonyl(methyl)amino]pyridine-4-carboxylate Chemical compound CC[C@H](C)NC1=CC(C(=O)OC)=CC(N(C)S(=O)(=O)C2CC2)=N1 LLVDUWSQFJROBX-JTQLQIEISA-N 0.000 description 1
- FPDIMFZVUVVBEH-VIFPVBQESA-N methyl 2-[[(2s)-butan-2-yl]amino]-6-[methyl(methylsulfonyl)amino]pyridine-4-carboxylate Chemical compound CC[C@H](C)NC1=CC(C(=O)OC)=CC(N(C)S(C)(=O)=O)=N1 FPDIMFZVUVVBEH-VIFPVBQESA-N 0.000 description 1
- DPWNPBXDXSTNTA-QMMMGPOBSA-N methyl 2-[[(2s)-butan-2-yl]amino]-6-methylsulfonylpyridine-4-carboxylate Chemical compound CC[C@H](C)NC1=CC(C(=O)OC)=CC(S(C)(=O)=O)=N1 DPWNPBXDXSTNTA-QMMMGPOBSA-N 0.000 description 1
- SVAYZLKHAVAKTN-JTQLQIEISA-N methyl 2-[[(2s)-butan-2-yl]amino]-6-propan-2-ylsulfonylpyridine-4-carboxylate Chemical compound CC[C@H](C)NC1=CC(C(=O)OC)=CC(S(=O)(=O)C(C)C)=N1 SVAYZLKHAVAKTN-JTQLQIEISA-N 0.000 description 1
- SUJVOSKRBYNLRZ-JTQLQIEISA-N methyl 2-[[(2s)-butan-2-yl]amino]-6-propylsulfanylpyridine-4-carboxylate Chemical compound CCCSC1=CC(C(=O)OC)=CC(N[C@@H](C)CC)=N1 SUJVOSKRBYNLRZ-JTQLQIEISA-N 0.000 description 1
- NZSWHOLIQDBGIA-JTQLQIEISA-N methyl 2-[[(2s)-butan-2-yl]amino]-6-propylsulfonylpyridine-4-carboxylate Chemical compound CCCS(=O)(=O)C1=CC(C(=O)OC)=CC(N[C@@H](C)CC)=N1 NZSWHOLIQDBGIA-JTQLQIEISA-N 0.000 description 1
- PVOPUARXHXVQHM-QMMMGPOBSA-N methyl 2-[[(2s)-butan-2-yl]amino]pyridine-4-carboxylate Chemical compound CC[C@H](C)NC1=CC(C(=O)OC)=CC=N1 PVOPUARXHXVQHM-QMMMGPOBSA-N 0.000 description 1
- HWQKLKREQSLNQG-UHFFFAOYSA-N methyl 2-[methyl(propyl)amino]-6-methylsulfonylpyridine-4-carboxylate Chemical compound CCCN(C)C1=CC(C(=O)OC)=CC(S(C)(=O)=O)=N1 HWQKLKREQSLNQG-UHFFFAOYSA-N 0.000 description 1
- VUMVDOQDOOEHTE-UHFFFAOYSA-N methyl 2-acetyl-6-chloropyridine-4-carboxylate Chemical compound COC(=O)C1=CC(Cl)=NC(C(C)=O)=C1 VUMVDOQDOOEHTE-UHFFFAOYSA-N 0.000 description 1
- NLIYIOXXVHNFCC-UHFFFAOYSA-N methyl 2-benzylsulfanyl-6-chloropyridine-4-carboxylate Chemical compound COC(=O)C1=CC(Cl)=NC(SCC=2C=CC=CC=2)=C1 NLIYIOXXVHNFCC-UHFFFAOYSA-N 0.000 description 1
- RALXPFFFCGSKKN-UHFFFAOYSA-N methyl 2-chloro-6-(1,1-difluoroethyl)pyridine-4-carboxylate Chemical compound COC(=O)C1=CC(Cl)=NC(C(C)(F)F)=C1 RALXPFFFCGSKKN-UHFFFAOYSA-N 0.000 description 1
- SPWCDEDSPLBYCI-UHFFFAOYSA-N methyl 2-chloro-6-(1,3-dioxan-2-yl)pyridine-4-carboxylate Chemical compound COC(=O)C1=CC(Cl)=NC(C2OCCCO2)=C1 SPWCDEDSPLBYCI-UHFFFAOYSA-N 0.000 description 1
- KAWLOQIXRAIMAU-UHFFFAOYSA-N methyl 2-chloro-6-(2,2-difluoropropyl)pyridine-4-carboxylate Chemical compound COC(=O)C1=CC(Cl)=NC(CC(C)(F)F)=C1 KAWLOQIXRAIMAU-UHFFFAOYSA-N 0.000 description 1
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- AYTSQHVTYYFJQV-UHFFFAOYSA-N methyl 2-chloro-6-[methyl(propyl)amino]pyridine-4-carboxylate Chemical compound CCCN(C)C1=CC(C(=O)OC)=CC(Cl)=N1 AYTSQHVTYYFJQV-UHFFFAOYSA-N 0.000 description 1
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- SDFRYLPDRDBYJQ-UHFFFAOYSA-N methyl 2-chloro-6-methylsulfonylpyridine-4-carboxylate Chemical compound COC(=O)C1=CC(Cl)=NC(S(C)(=O)=O)=C1 SDFRYLPDRDBYJQ-UHFFFAOYSA-N 0.000 description 1
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- RZWQDAUIUBVCDD-UHFFFAOYSA-M sodium;benzenethiolate Chemical compound [Na+].[S-]C1=CC=CC=C1 RZWQDAUIUBVCDD-UHFFFAOYSA-M 0.000 description 1
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- PORWMNRCUJJQNO-UHFFFAOYSA-N tellurium atom Chemical compound [Te] PORWMNRCUJJQNO-UHFFFAOYSA-N 0.000 description 1
- AXZZSWKWDQMEHZ-IDZRBWSNSA-N tert-butyl (2r)-2-[(1s,2r)-2-(dibenzylamino)-1-hydroxy-3-phenylpropyl]pyrrolidine-1-carboxylate Chemical compound CC(C)(C)OC(=O)N1CCC[C@@H]1[C@@H](O)[C@H](N(CC=1C=CC=CC=1)CC=1C=CC=CC=1)CC1=CC=CC=C1 AXZZSWKWDQMEHZ-IDZRBWSNSA-N 0.000 description 1
- HTGXWROTQKRYIE-OAGGEKHMSA-N tert-butyl (2r)-2-[(1s,2r)-2-amino-1-hydroxy-3-phenylpropyl]pyrrolidine-1-carboxylate Chemical compound CC(C)(C)OC(=O)N1CCC[C@@H]1[C@@H](O)[C@H](N)CC1=CC=CC=C1 HTGXWROTQKRYIE-OAGGEKHMSA-N 0.000 description 1
- AXZZSWKWDQMEHZ-DYIKCSJPSA-N tert-butyl (2r)-2-[(1s,2s)-2-(dibenzylamino)-1-hydroxy-3-phenylpropyl]pyrrolidine-1-carboxylate Chemical compound CC(C)(C)OC(=O)N1CCC[C@@H]1[C@@H](O)[C@@H](N(CC=1C=CC=CC=1)CC=1C=CC=CC=1)CC1=CC=CC=C1 AXZZSWKWDQMEHZ-DYIKCSJPSA-N 0.000 description 1
- OASJCUKJGZXGJB-YKILCQELSA-N tert-butyl (2r)-2-[(1s,2s)-2-[bis[(2-methylphenyl)methyl]amino]-3-(3,5-difluorophenyl)-1-hydroxypropyl]pyrrolidine-1-carboxylate Chemical compound CC1=CC=CC=C1CN([C@@H](CC=1C=C(F)C=C(F)C=1)[C@H](O)[C@@H]1N(CCC1)C(=O)OC(C)(C)C)CC1=CC=CC=C1C OASJCUKJGZXGJB-YKILCQELSA-N 0.000 description 1
- IVLMNCDJHTXENB-OTWHNJEPSA-N tert-butyl (2r)-2-[(1s,2s)-2-acetamido-3-(3,5-difluorophenyl)-1-hydroxypropyl]piperidine-1-carboxylate Chemical compound C([C@H](NC(=O)C)[C@H](O)[C@@H]1N(CCCC1)C(=O)OC(C)(C)C)C1=CC(F)=CC(F)=C1 IVLMNCDJHTXENB-OTWHNJEPSA-N 0.000 description 1
- QHLDTEILDOGJST-BBWFWOEESA-N tert-butyl (2r)-2-[(1s,2s)-2-amino-3-(3,5-difluorophenyl)-1-hydroxypropyl]piperidine-1-carboxylate Chemical compound CC(C)(C)OC(=O)N1CCCC[C@@H]1[C@@H](O)[C@@H](N)CC1=CC(F)=CC(F)=C1 QHLDTEILDOGJST-BBWFWOEESA-N 0.000 description 1
- HPMDGCWVWAKGEX-HUUCEWRRSA-N tert-butyl (2r,4r)-2-(hydroxymethyl)-4-phenylmethoxypyrrolidine-1-carboxylate Chemical compound C1[C@H](CO)N(C(=O)OC(C)(C)C)C[C@@H]1OCC1=CC=CC=C1 HPMDGCWVWAKGEX-HUUCEWRRSA-N 0.000 description 1
- SUGVGSHHVMANBT-BXXSPATCSA-N tert-butyl (2r,4r)-2-[(1r,2s)-3-(3,5-difluorophenyl)-1-hydroxy-2-nitropropyl]-4-(3-methoxyphenoxy)pyrrolidine-1-carboxylate Chemical compound COC1=CC=CC(O[C@H]2CN([C@@H]([C@@H](O)[C@H](CC=3C=C(F)C=C(F)C=3)[N+]([O-])=O)C2)C(=O)OC(C)(C)C)=C1 SUGVGSHHVMANBT-BXXSPATCSA-N 0.000 description 1
- NLLCSJNNJAPRHT-ACESQOTJSA-N tert-butyl (2r,4r)-2-[(1s,2s)-2-amino-3-(3,5-difluorophenyl)-1-hydroxypropyl]-4-phenylmethoxypyrrolidine-1-carboxylate Chemical compound C([C@H](N)[C@H](O)[C@H]1C[C@H](CN1C(=O)OC(C)(C)C)OCC=1C=CC=CC=1)C1=CC(F)=CC(F)=C1 NLLCSJNNJAPRHT-ACESQOTJSA-N 0.000 description 1
- UNGJMEXGBILRRO-YSTOQKLRSA-N tert-butyl (2r,4r)-2-[(4s,5s)-3-acetyl-4-[(3,5-difluorophenyl)methyl]-2,2-dimethyl-1,3-oxazolidin-5-yl]-4-hydroxypyrrolidine-1-carboxylate Chemical compound C([C@@H]1N(C(O[C@@H]1[C@@H]1N(C[C@H](O)C1)C(=O)OC(C)(C)C)(C)C)C(=O)C)C1=CC(F)=CC(F)=C1 UNGJMEXGBILRRO-YSTOQKLRSA-N 0.000 description 1
- AKGPLQVNHJXHHB-HUUCEWRRSA-N tert-butyl (2r,4r)-2-formyl-4-phenylmethoxypyrrolidine-1-carboxylate Chemical compound C1[C@H](C=O)N(C(=O)OC(C)(C)C)C[C@@H]1OCC1=CC=CC=C1 AKGPLQVNHJXHHB-HUUCEWRRSA-N 0.000 description 1
- ROEMZCLHRRRKGF-HTQZYQBOSA-N tert-butyl (2r,4r)-4-fluoro-2-(hydroxymethyl)pyrrolidine-1-carboxylate Chemical compound CC(C)(C)OC(=O)N1C[C@H](F)C[C@@H]1CO ROEMZCLHRRRKGF-HTQZYQBOSA-N 0.000 description 1
- PABLOPMZCFQFHB-HTQZYQBOSA-N tert-butyl (2r,4r)-4-fluoro-2-formylpyrrolidine-1-carboxylate Chemical compound CC(C)(C)OC(=O)N1C[C@H](F)C[C@@H]1C=O PABLOPMZCFQFHB-HTQZYQBOSA-N 0.000 description 1
- OIIMLHZIZPREOV-JONQDZQNSA-N tert-butyl (2r,4s)-2-[(1s,2s)-2-amino-1-hydroxy-3-phenylpropyl]-4-fluoropyrrolidine-1-carboxylate Chemical compound CC(C)(C)OC(=O)N1C[C@@H](F)C[C@@H]1[C@@H](O)[C@@H](N)CC1=CC=CC=C1 OIIMLHZIZPREOV-JONQDZQNSA-N 0.000 description 1
- ROEMZCLHRRRKGF-JGVFFNPUSA-N tert-butyl (2r,4s)-4-fluoro-2-(hydroxymethyl)pyrrolidine-1-carboxylate Chemical compound CC(C)(C)OC(=O)N1C[C@@H](F)C[C@@H]1CO ROEMZCLHRRRKGF-JGVFFNPUSA-N 0.000 description 1
- ZSENFICTGYPBLC-FZKCQIBNSA-N tert-butyl (2r,4s)-4-fluoro-2-[(1s,2s)-1-hydroxy-2-nitro-3-phenylpropyl]pyrrolidine-1-carboxylate Chemical compound CC(C)(C)OC(=O)N1C[C@@H](F)C[C@@H]1[C@H](O)[C@@H]([N+]([O-])=O)CC1=CC=CC=C1 ZSENFICTGYPBLC-FZKCQIBNSA-N 0.000 description 1
- PABLOPMZCFQFHB-JGVFFNPUSA-N tert-butyl (2r,4s)-4-fluoro-2-formylpyrrolidine-1-carboxylate Chemical compound CC(C)(C)OC(=O)N1C[C@@H](F)C[C@@H]1C=O PABLOPMZCFQFHB-JGVFFNPUSA-N 0.000 description 1
- SUECTKVSIDXQQE-SSDOTTSWSA-N tert-butyl (3r)-3-fluoropyrrolidine-1-carboxylate Chemical compound CC(C)(C)OC(=O)N1CC[C@@H](F)C1 SUECTKVSIDXQQE-SSDOTTSWSA-N 0.000 description 1
- PLRVIRHWKQKSAK-UHFFFAOYSA-N tert-butyl 2,6-dichloropyridine-4-carboxylate Chemical compound CC(C)(C)OC(=O)C1=CC(Cl)=NC(Cl)=C1 PLRVIRHWKQKSAK-UHFFFAOYSA-N 0.000 description 1
- COHXIKONXSGVCA-UHFFFAOYSA-N tert-butyl 2-(cyclopropylamino)-6-cyclopropylsulfonylpyridine-4-carboxylate Chemical compound N=1C(S(=O)(=O)C2CC2)=CC(C(=O)OC(C)(C)C)=CC=1NC1CC1 COHXIKONXSGVCA-UHFFFAOYSA-N 0.000 description 1
- JEBOAVCNIBDCSV-AJQTZOPKSA-N tert-butyl 2-[(1s,2s)-2-[bis[(2-methylphenyl)methyl]amino]-3-(3,5-difluorophenyl)-1-hydroxypropyl]pyrrole-1-carboxylate Chemical compound CC1=CC=CC=C1CN([C@@H](CC=1C=C(F)C=C(F)C=1)[C@H](O)C=1N(C=CC=1)C(=O)OC(C)(C)C)CC1=CC=CC=C1C JEBOAVCNIBDCSV-AJQTZOPKSA-N 0.000 description 1
- JSOMVCDXPUXKIC-UHFFFAOYSA-N tert-butyl 3-oxopyrrolidine-1-carboxylate Chemical compound CC(C)(C)OC(=O)N1CCC(=O)C1 JSOMVCDXPUXKIC-UHFFFAOYSA-N 0.000 description 1
- UOUFRTFWWBCVPV-UHFFFAOYSA-N tert-butyl 4-(2,4-dioxo-1H-thieno[3,2-d]pyrimidin-3-yl)piperidine-1-carboxylate Chemical compound CC(C)(C)OC(=O)N1CCC(CC1)n1c(=O)[nH]c2ccsc2c1=O UOUFRTFWWBCVPV-UHFFFAOYSA-N 0.000 description 1
- OQJFNQDUSDUOLR-JDXGNMNLSA-N tert-butyl 5-[(1s,2s)-2-(dibenzylamino)-1-hydroxy-3-phenylpropyl]-4-fluoro-2,3-dihydropyrrole-1-carboxylate Chemical compound CC(C)(C)OC(=O)N1CCC(F)=C1[C@@H](O)[C@@H](N(CC=1C=CC=CC=1)CC=1C=CC=CC=1)CC1=CC=CC=C1 OQJFNQDUSDUOLR-JDXGNMNLSA-N 0.000 description 1
- FQFILJKFZCVHNH-UHFFFAOYSA-N tert-butyl n-[3-[(5-bromo-2-chloropyrimidin-4-yl)amino]propyl]carbamate Chemical compound CC(C)(C)OC(=O)NCCCNC1=NC(Cl)=NC=C1Br FQFILJKFZCVHNH-UHFFFAOYSA-N 0.000 description 1
- 125000000037 tert-butyldiphenylsilyl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1[Si]([H])([*]C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 150000003509 tertiary alcohols Chemical class 0.000 description 1
- JRMUNVKIHCOMHV-UHFFFAOYSA-M tetrabutylammonium bromide Chemical compound [Br-].CCCC[N+](CCCC)(CCCC)CCCC JRMUNVKIHCOMHV-UHFFFAOYSA-M 0.000 description 1
- 125000004632 tetrahydrothiopyranyl group Chemical group S1C(CCCC1)* 0.000 description 1
- CFOAUYCPAUGDFF-UHFFFAOYSA-N tosmic Chemical compound CC1=CC=C(S(=O)(=O)C[N+]#[C-])C=C1 CFOAUYCPAUGDFF-UHFFFAOYSA-N 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- PIILXFBHQILWPS-UHFFFAOYSA-N tributyltin Chemical compound CCCC[Sn](CCCC)CCCC PIILXFBHQILWPS-UHFFFAOYSA-N 0.000 description 1
- ILWRPSCZWQJDMK-UHFFFAOYSA-N triethylazanium;chloride Chemical compound Cl.CCN(CC)CC ILWRPSCZWQJDMK-UHFFFAOYSA-N 0.000 description 1
- 125000000025 triisopropylsilyl group Chemical group C(C)(C)[Si](C(C)C)(C(C)C)* 0.000 description 1
- 230000002792 vascular Effects 0.000 description 1
- 238000013022 venting Methods 0.000 description 1
- LVLANIHJQRZTPY-UHFFFAOYSA-N vinyl carbamate Chemical compound NC(=O)OC=C LVLANIHJQRZTPY-UHFFFAOYSA-N 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
- A61P25/16—Anti-Parkinson drugs
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/14—Vasoprotectives; Antihaemorrhoidals; Drugs for varicose therapy; Capillary stabilisers
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D207/08—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon radicals, substituted by hetero atoms, attached to ring carbon atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D207/10—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D207/12—Oxygen or sulfur atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/08—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms
- C07D211/18—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D211/26—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by nitrogen atoms
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D211/40—Oxygen atoms
- C07D211/42—Oxygen atoms attached in position 3 or 5
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- C07D217/00—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
- C07D217/12—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with radicals, substituted by hetero atoms, attached to carbon atoms of the nitrogen-containing ring
- C07D217/18—Aralkyl radicals
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- 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
- C07D241/04—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
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- 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
- C07D241/06—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having one or two double bonds between ring members or between ring members and non-ring members
- C07D241/08—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having one or two double bonds between ring members or between ring members and non-ring members with oxygen atoms directly attached to ring carbon atoms
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- 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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
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- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
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- C—CHEMISTRY; METALLURGY
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- 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
- C07D417/12—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 chain containing hetero atoms as chain links
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
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- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/08—Bridged systems
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- General Chemical & Material Sciences (AREA)
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- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Psychiatry (AREA)
- Hospice & Palliative Care (AREA)
- Vascular Medicine (AREA)
- Psychology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyrrole Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Indole Compounds (AREA)
- Hydrogenated Pyridines (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US56453804P | 2004-04-22 | 2004-04-22 | |
| PCT/US2005/012191 WO2005108358A2 (en) | 2004-04-22 | 2005-04-08 | Pyrrolidine derivatives useful as bace inhibitors |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2007533741A true JP2007533741A (ja) | 2007-11-22 |
| JP2007533741A5 JP2007533741A5 (ja) | 2011-07-07 |
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| Application Number | Title | Priority Date | Filing Date |
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| JP2007509507A Pending JP2007533740A (ja) | 2004-04-22 | 2005-04-08 | Bace阻害剤としてのアミド |
| JP2007509508A Ceased JP2007533741A (ja) | 2004-04-22 | 2005-04-08 | Bace阻害剤 |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
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| JP2007509507A Pending JP2007533740A (ja) | 2004-04-22 | 2005-04-08 | Bace阻害剤としてのアミド |
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| Country | Link |
|---|---|
| US (1) | US7618978B2 (enExample) |
| EP (2) | EP1740575A2 (enExample) |
| JP (2) | JP2007533740A (enExample) |
| WO (2) | WO2005108358A2 (enExample) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2008507538A (ja) * | 2004-07-22 | 2008-03-13 | シェーリング コーポレイション | 置換アミドβセクレターゼインヒビター |
| JP2012521421A (ja) * | 2009-03-25 | 2012-09-13 | コメンティス,インコーポレーテッド | β−セクレターゼ活性を阻害するピロリジン化合物及びその使用方法 |
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- 2005-04-08 WO PCT/US2005/012191 patent/WO2005108358A2/en not_active Ceased
- 2005-04-08 EP EP05736358A patent/EP1740573A1/en not_active Withdrawn
- 2005-04-08 JP JP2007509507A patent/JP2007533740A/ja active Pending
- 2005-04-08 JP JP2007509508A patent/JP2007533741A/ja not_active Ceased
- 2005-04-08 US US10/599,125 patent/US7618978B2/en not_active Expired - Fee Related
- 2005-04-08 WO PCT/US2005/012189 patent/WO2005108391A1/en not_active Ceased
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| JP2008507538A (ja) * | 2004-07-22 | 2008-03-13 | シェーリング コーポレイション | 置換アミドβセクレターゼインヒビター |
| JP2012521421A (ja) * | 2009-03-25 | 2012-09-13 | コメンティス,インコーポレーテッド | β−セクレターゼ活性を阻害するピロリジン化合物及びその使用方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2007533740A (ja) | 2007-11-22 |
| EP1740575A2 (en) | 2007-01-10 |
| EP1740573A1 (en) | 2007-01-10 |
| US7618978B2 (en) | 2009-11-17 |
| US20070225372A1 (en) | 2007-09-27 |
| WO2005108358A3 (en) | 2006-05-26 |
| WO2005108358A2 (en) | 2005-11-17 |
| WO2005108391A1 (en) | 2005-11-17 |
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