JP2006517971A5

JP2006517971A5 -

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Publication number: JP2006517971A5
Authority: JP; Japan
Prior art keywords: compound; mmol; group; alkyl; ylene
Prior art date: 2004-02-13
Legal status : Withdrawn

Application number

JP2006503544A

Other languages

English (en)

Japanese (ja)

Other versions

JP2006517971A (ja

Filing date

2004-02-13

Publication date

2007-03-29

2004-02-13 Application filed filed Critical

2004-02-13 Priority claimed from PCT/US2004/004224 external-priority patent/WO2004074276A1/en

2006-08-03 Publication of JP2006517971A publication Critical patent/JP2006517971A/ja

2007-03-29 Publication of JP2006517971A5 publication Critical patent/JP2006517971A5/ja

Status Withdrawn legal-status Critical Current

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150000001875 compounds Chemical class 0.000 claims description 416
239000000203 mixture Substances 0.000 claims description 180
-1 (biphenyl-2-yl) aminocarbonyloxy Chemical group 0.000 claims description 172
239000001257 hydrogen Substances 0.000 claims description 127
229910052739 hydrogen Inorganic materials 0.000 claims description 127
125000000217 alkyl group Chemical group 0.000 claims description 123
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 104
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical group N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 95
150000003839 salts Chemical class 0.000 claims description 85
238000000034 method Methods 0.000 claims description 72
229910052757 nitrogen Inorganic materials 0.000 claims description 72
230000000694 effects Effects 0.000 claims description 61
125000001424 substituent group Chemical group 0.000 claims description 59
239000008194 pharmaceutical composition Substances 0.000 claims description 50
125000005843 halogen group Chemical group 0.000 claims description 46
239000012453 solvate Substances 0.000 claims description 42
239000000048 adrenergic agonist Substances 0.000 claims description 40
229940126157 adrenergic receptor agonist Drugs 0.000 claims description 35
229940121948 Muscarinic receptor antagonist Drugs 0.000 claims description 33
125000004432 carbon atom Chemical group C* 0.000 claims description 30
125000000753 cycloalkyl group Chemical group 0.000 claims description 29
239000003149 muscarinic antagonist Substances 0.000 claims description 28
125000004433 nitrogen atom Chemical group N* 0.000 claims description 28
125000002947 alkylene group Chemical group 0.000 claims description 26
125000003386 piperidinyl group Chemical group 0.000 claims description 26
208000019693 Lung disease Diseases 0.000 claims description 24
125000003342 alkenyl group Chemical group 0.000 claims description 20
125000005842 heteroatom Chemical group 0.000 claims description 20
239000003814 drug Substances 0.000 claims description 19
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 19
102000014415 Muscarinic acetylcholine receptor Human genes 0.000 claims description 17
108050003473 Muscarinic acetylcholine receptor Proteins 0.000 claims description 17
125000000623 heterocyclic group Chemical group 0.000 claims description 17
238000011282 treatment Methods 0.000 claims description 17
125000003545 alkoxy group Chemical group 0.000 claims description 16
125000000304 alkynyl group Chemical group 0.000 claims description 16
125000003118 aryl group Chemical group 0.000 claims description 16
229910052760 oxygen Inorganic materials 0.000 claims description 16
108060003345 Adrenergic Receptor Proteins 0.000 claims description 14
102000017910 Adrenergic receptor Human genes 0.000 claims description 14
125000004093 cyano group Chemical group *C#N 0.000 claims description 14
125000001153 fluoro group Chemical group F* 0.000 claims description 14
125000001072 heteroaryl group Chemical group 0.000 claims description 14
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 12
125000004450 alkenylene group Chemical group 0.000 claims description 12
125000003277 amino group Chemical group 0.000 claims description 12
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 12
239000001301 oxygen Chemical group 0.000 claims description 12
229910052717 sulfur Chemical group 0.000 claims description 12
239000011593 sulfur Chemical group 0.000 claims description 12
208000006545 Chronic Obstructive Pulmonary Disease Diseases 0.000 claims description 11
239000003795 chemical substances by application Substances 0.000 claims description 10
208000006673 asthma Diseases 0.000 claims description 9
230000027455 binding Effects 0.000 claims description 8
238000009739 binding Methods 0.000 claims description 8
230000005764 inhibitory process Effects 0.000 claims description 7
230000008569 process Effects 0.000 claims description 7
238000002560 therapeutic procedure Methods 0.000 claims description 7
239000003937 drug carrier Substances 0.000 claims description 6
239000004215 Carbon black (E152) Substances 0.000 claims description 4
229930195733 hydrocarbon Natural products 0.000 claims description 4
238000004519 manufacturing process Methods 0.000 claims description 4
239000002587 phosphodiesterase IV inhibitor Substances 0.000 claims description 4
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 4
125000003700 epoxy group Chemical group 0.000 claims description 3
239000002294 steroidal antiinflammatory agent Substances 0.000 claims description 3
LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims description 3
125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims description 3
125000001183 hydrocarbyl group Chemical group 0.000 claims 8
CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims 1
230000003796 beauty Effects 0.000 claims 1
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 358
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 225
238000002360 preparation method Methods 0.000 description 220
239000011541 reaction mixture Substances 0.000 description 169
239000000047 product Substances 0.000 description 155
239000000243 solution Substances 0.000 description 147
230000002829 reductive effect Effects 0.000 description 130
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 118
239000002904 solvent Substances 0.000 description 118
UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 107
CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 102
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 94
238000006243 chemical reaction Methods 0.000 description 87
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 75
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 75
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 72
KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 70
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 70
239000007787 solid Substances 0.000 description 66
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 61
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 60
JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-Diisopropylethylamine (DIPEA) Chemical compound CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 description 58
229910052943 magnesium sulfate Inorganic materials 0.000 description 51
235000019341 magnesium sulphate Nutrition 0.000 description 51
239000012044 organic layer Substances 0.000 description 51
229920006395 saturated elastomer Polymers 0.000 description 49
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 46
235000017557 sodium bicarbonate Nutrition 0.000 description 46
229910000030 sodium bicarbonate Inorganic materials 0.000 description 46
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 45
235000019439 ethyl acetate Nutrition 0.000 description 42
238000004128 high performance liquid chromatography Methods 0.000 description 42
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 41
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 37
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 37
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 37
QMOVGVNKXUTCQU-UHFFFAOYSA-N (2-phenylphenyl)carbamic acid Chemical compound OC(=O)NC1=CC=CC=C1C1=CC=CC=C1 QMOVGVNKXUTCQU-UHFFFAOYSA-N 0.000 description 36
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 33
DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 32
239000012074 organic phase Substances 0.000 description 31
150000002430 hydrocarbons Chemical group 0.000 description 30
239000012267 brine Substances 0.000 description 28
239000010410 layer Substances 0.000 description 28
125000006239 protecting group Chemical group 0.000 description 28
HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 28
235000019441 ethanol Nutrition 0.000 description 27
125000002887 hydroxy group Chemical group [H]O* 0.000 description 26
125000004482 piperidin-4-yl group Chemical group N1CCC(CC1)* 0.000 description 26
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 25
239000000543 intermediate Substances 0.000 description 25
238000000746 purification Methods 0.000 description 24
QTBSBXVTEAMEQO-UHFFFAOYSA-N acetic acid Substances CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 23
125000000031 ethylamino group Chemical group [H]C([H])([H])C([H])([H])N([H])[*] 0.000 description 23
125000004435 hydrogen atom Chemical group [H]* 0.000 description 23
239000003921 oil Substances 0.000 description 22
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 21
238000004895 liquid chromatography mass spectrometry Methods 0.000 description 21
235000019198 oils Nutrition 0.000 description 21
FVAUCKIRQBBSSJ-UHFFFAOYSA-M sodium iodide Chemical compound [Na+].[I-] FVAUCKIRQBBSSJ-UHFFFAOYSA-M 0.000 description 21
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 20
229910052799 carbon Inorganic materials 0.000 description 20
150000002431 hydrogen Chemical class 0.000 description 20
239000011734 sodium Substances 0.000 description 20
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 19
239000013543 active substance Substances 0.000 description 18
229910052763 palladium Inorganic materials 0.000 description 18
239000002245 particle Substances 0.000 description 18
239000000843 powder Substances 0.000 description 18
239000002253 acid Substances 0.000 description 17
238000009472 formulation Methods 0.000 description 17
IKGLACJFEHSFNN-UHFFFAOYSA-N hydron;triethylazanium;trifluoride Chemical compound F.F.F.CCN(CC)CC IKGLACJFEHSFNN-UHFFFAOYSA-N 0.000 description 17
238000002953 preparative HPLC Methods 0.000 description 17
239000000725 suspension Substances 0.000 description 17
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 16
239000012321 sodium triacetoxyborohydride Substances 0.000 description 16
238000003756 stirring Methods 0.000 description 16
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 15
239000012298 atmosphere Substances 0.000 description 15
125000004429 atom Chemical group 0.000 description 14
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 14
239000012043 crude product Substances 0.000 description 14
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 14
239000011780 sodium chloride Substances 0.000 description 14
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 13
239000004480 active ingredient Substances 0.000 description 13
150000001721 carbon Chemical group 0.000 description 13
239000003638 chemical reducing agent Substances 0.000 description 13
RWTNPBWLLIMQHL-UHFFFAOYSA-N fexofenadine Chemical group C1=CC(C(C)(C(O)=O)C)=CC=C1C(O)CCCN1CCC(C(O)(C=2C=CC=CC=2)C=2C=CC=CC=2)CC1 RWTNPBWLLIMQHL-UHFFFAOYSA-N 0.000 description 13
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 13
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 13
238000010898 silica gel chromatography Methods 0.000 description 13
125000001309 chloro group Chemical group Cl* 0.000 description 12
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 12
238000004440 column chromatography Methods 0.000 description 12
125000005549 heteroarylene group Chemical group 0.000 description 12
RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 12
239000002002 slurry Substances 0.000 description 12
JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 12
AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 11
125000000732 arylene group Chemical group 0.000 description 11
125000001246 bromo group Chemical group Br* 0.000 description 11
239000003054 catalyst Substances 0.000 description 11
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 11
238000003818 flash chromatography Methods 0.000 description 11
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 11
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 11
YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 10
ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical class C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 10
201000010099 disease Diseases 0.000 description 10
125000002346 iodo group Chemical group I* 0.000 description 10
239000000546 pharmaceutical excipient Substances 0.000 description 10
239000012071 phase Substances 0.000 description 10
125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 10
GUBGYTABKSRVRQ-XLOQQCSPSA-N Alpha-Lactose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-N 0.000 description 9
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 9
GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 9
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 9
125000004419 alkynylene group Chemical group 0.000 description 9
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 9
125000002993 cycloalkylene group Chemical group 0.000 description 9
150000002148 esters Chemical class 0.000 description 9
239000008101 lactose Substances 0.000 description 9
229910052751 metal Inorganic materials 0.000 description 9
239000002184 metal Substances 0.000 description 9
229940071648 metered dose inhaler Drugs 0.000 description 9
GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 8
229960000583 acetic acid Drugs 0.000 description 8
238000004458 analytical method Methods 0.000 description 8
WGQKYBSKWIADBV-UHFFFAOYSA-N benzylamine Chemical compound NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 description 8
239000003153 chemical reaction reagent Substances 0.000 description 8
125000000524 functional group Chemical group 0.000 description 8
239000003701 inert diluent Substances 0.000 description 8
239000004615 ingredient Substances 0.000 description 8
125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 8
229940124597 therapeutic agent Drugs 0.000 description 8
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 7
CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 description 7
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 7
BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 description 7
230000007883 bronchodilation Effects 0.000 description 7
239000002775 capsule Substances 0.000 description 7
229940112141 dry powder inhaler Drugs 0.000 description 7
239000000706 filtrate Substances 0.000 description 7
239000000463 material Substances 0.000 description 7
125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 7
229910000027 potassium carbonate Inorganic materials 0.000 description 7
102000005962 receptors Human genes 0.000 description 7
108020003175 receptors Proteins 0.000 description 7
235000009518 sodium iodide Nutrition 0.000 description 7
239000007858 starting material Substances 0.000 description 7
125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 7
SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 description 6
IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 6
WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 6
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 6
NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 6
GXCLVBGFBYZDAG-UHFFFAOYSA-N N-[2-(1H-indol-3-yl)ethyl]-N-methylprop-2-en-1-amine Chemical compound CN(CCC1=CNC2=C1C=CC=C2)CC=C GXCLVBGFBYZDAG-UHFFFAOYSA-N 0.000 description 6
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 6
KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 6
229940124599 anti-inflammatory drug Drugs 0.000 description 6
125000004956 cyclohexylene group Chemical group 0.000 description 6
150000005828 hydrofluoroalkanes Chemical class 0.000 description 6
235000010445 lecithin Nutrition 0.000 description 6
239000000787 lecithin Substances 0.000 description 6
229940067606 lecithin Drugs 0.000 description 6
XTEGVFVZDVNBPF-UHFFFAOYSA-N naphthalene-1,5-disulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1S(O)(=O)=O XTEGVFVZDVNBPF-UHFFFAOYSA-N 0.000 description 6
239000003380 propellant Substances 0.000 description 6
238000004007 reversed phase HPLC Methods 0.000 description 6
125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 6
238000012360 testing method Methods 0.000 description 6
FBPINGSGHKXIQA-UHFFFAOYSA-N 2-amino-3-(2-carboxyethylsulfanyl)propanoic acid Chemical compound OC(=O)C(N)CSCCC(O)=O FBPINGSGHKXIQA-UHFFFAOYSA-N 0.000 description 5
MSYGAHOHLUJIKV-UHFFFAOYSA-N 3,5-dimethyl-1-(3-nitrophenyl)-1h-pyrazole-4-carboxylic acid ethyl ester Chemical compound CC1=C(C(=O)OCC)C(C)=NN1C1=CC=CC([N+]([O-])=O)=C1 MSYGAHOHLUJIKV-UHFFFAOYSA-N 0.000 description 5
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 5
IVOMOUWHDPKRLL-KQYNXXCUSA-N Cyclic adenosine monophosphate Chemical compound C([C@H]1O2)OP(O)(=O)O[C@H]1[C@@H](O)[C@@H]2N1C(N=CN=C2N)=C2N=C1 IVOMOUWHDPKRLL-KQYNXXCUSA-N 0.000 description 5
XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 5
239000007821 HATU Substances 0.000 description 5
XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 5
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JP2006503544A 2003-02-14 2004-02-13 β２アドレナリン作用性レセプターアゴニスト活性およびムスカリン性レセプターアンタゴニスト活性を有するビフェニル誘導体 Withdrawn JP2006517971A (ja)