NO325236B1 - Cykliseringsfremgangsmatetrinn for fremstilling av kinoloner og naftyridiner - Google Patents

Cykliseringsfremgangsmatetrinn for fremstilling av kinoloner og naftyridiner Download PDF

Info

Publication number: NO325236B1
Authority: NO; Norway
Prior art keywords: alkyl; aryl; esters; formula; hydrogen
Prior art date: 2000-12-14

Application number

NO20032667A

Other languages

English (en)

Norwegian (no)

Other versions

NO20032667D0 (no

NO20032667L (no

Inventor

Sreenivasa Reddy Mundla

Jared Lynn Randall

Original Assignee

Procter & Gamble

Priority date (The priority date 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 date listed.)

2000-12-14

Filing date

2003-06-12

Publication date

2008-03-03

2003-06-12 Application filed by Procter & Gamble filed Critical Procter & Gamble

2003-06-12 Publication of NO20032667D0 publication Critical patent/NO20032667D0/no

2003-08-14 Publication of NO20032667L publication Critical patent/NO20032667L/no

2008-03-03 Publication of NO325236B1 publication Critical patent/NO325236B1/no

Links

238000000034 method Methods 0.000 title claims abstract description 74
150000007660 quinolones Chemical class 0.000 title description 11
238000007363 ring formation reaction Methods 0.000 title description 9
238000002360 preparation method Methods 0.000 title description 3
150000005054 naphthyridines Chemical class 0.000 title 1
150000001875 compounds Chemical class 0.000 claims abstract description 55
230000008569 process Effects 0.000 claims abstract description 17
239000003153 chemical reaction reagent Substances 0.000 claims abstract description 16
-1 Ci- to Cis-alkoxy Chemical group 0.000 claims description 57
125000000217 alkyl group Chemical group 0.000 claims description 55
125000003118 aryl group Chemical group 0.000 claims description 50
150000003839 salts Chemical class 0.000 claims description 37
239000001257 hydrogen Substances 0.000 claims description 36
229910052739 hydrogen Inorganic materials 0.000 claims description 36
125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 36
150000002148 esters Chemical class 0.000 claims description 30
125000000623 heterocyclic group Chemical group 0.000 claims description 29
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 27
125000005843 halogen group Chemical group 0.000 claims description 24
229910052799 carbon Inorganic materials 0.000 claims description 23
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 23
125000004104 aryloxy group Chemical group 0.000 claims description 22
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims description 21
125000003545 alkoxy group Chemical group 0.000 claims description 21
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 20
125000000753 cycloalkyl group Chemical group 0.000 claims description 19
125000004404 heteroalkyl group Chemical group 0.000 claims description 19
150000001408 amides Chemical class 0.000 claims description 18
125000000592 heterocycloalkyl group Chemical group 0.000 claims description 18
125000005842 heteroatom Chemical group 0.000 claims description 16
125000004429 atom Chemical group 0.000 claims description 15
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 15
125000004093 cyano group Chemical group *C#N 0.000 claims description 15
125000004414 alkyl thio group Chemical group 0.000 claims description 14
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 14
125000001424 substituent group Chemical group 0.000 claims description 14
125000003368 amide group Chemical group 0.000 claims description 13
125000005251 aryl acyl group Chemical group 0.000 claims description 13
125000001769 aryl amino group Chemical group 0.000 claims description 13
125000005110 aryl thio group Chemical group 0.000 claims description 13
125000001072 heteroaryl group Chemical group 0.000 claims description 13
SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 claims description 12
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 12
150000007860 aryl ester derivatives Chemical class 0.000 claims description 12
239000002904 solvent Substances 0.000 claims description 12
239000000203 mixture Substances 0.000 claims description 11
125000005257 alkyl acyl group Chemical group 0.000 claims description 10
125000004391 aryl sulfonyl group Chemical group 0.000 claims description 10
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims description 9
230000003287 optical effect Effects 0.000 claims description 9
125000000446 sulfanediyl group Chemical group *S* 0.000 claims description 9
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 8
125000001054 5 membered carbocyclic group Chemical group 0.000 claims description 7
125000004008 6 membered carbocyclic group Chemical group 0.000 claims description 7
150000003949 imides Chemical class 0.000 claims description 7
229910052757 nitrogen Inorganic materials 0.000 claims description 6
125000006413 ring segment Chemical group 0.000 claims description 6
125000003277 amino group Chemical group 0.000 claims description 5
229910052736 halogen Inorganic materials 0.000 claims description 5
150000002367 halogens Chemical class 0.000 claims description 5
SIOVKLKJSOKLIF-HJWRWDBZSA-N trimethylsilyl (1z)-n-trimethylsilylethanimidate Chemical compound C[Si](C)(C)OC(/C)=N\[Si](C)(C)C SIOVKLKJSOKLIF-HJWRWDBZSA-N 0.000 claims description 5
XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 claims description 4
XCOBLONWWXQEBS-KPKJPENVSA-N N,O-bis(trimethylsilyl)trifluoroacetamide Chemical compound C[Si](C)(C)O\C(C(F)(F)F)=N\[Si](C)(C)C XCOBLONWWXQEBS-KPKJPENVSA-N 0.000 claims description 4
MSPCIZMDDUQPGJ-UHFFFAOYSA-N N-methyl-N-(trimethylsilyl)trifluoroacetamide Chemical compound C[Si](C)(C)N(C)C(=O)C(F)(F)F MSPCIZMDDUQPGJ-UHFFFAOYSA-N 0.000 claims description 4
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 4
125000002837 carbocyclic group Chemical group 0.000 claims description 4
DCFKHNIGBAHNSS-UHFFFAOYSA-N chloro(triethyl)silane Chemical compound CC[Si](Cl)(CC)CC DCFKHNIGBAHNSS-UHFFFAOYSA-N 0.000 claims description 4
IJOOHPMOJXWVHK-UHFFFAOYSA-N chlorotrimethylsilane Chemical compound C[Si](C)(C)Cl IJOOHPMOJXWVHK-UHFFFAOYSA-N 0.000 claims description 4
FFUAGWLWBBFQJT-UHFFFAOYSA-N hexamethyldisilazane Chemical compound C[Si](C)(C)N[Si](C)(C)C FFUAGWLWBBFQJT-UHFFFAOYSA-N 0.000 claims description 4
MHYGQXWCZAYSLJ-UHFFFAOYSA-N tert-butyl-chloro-diphenylsilane Chemical compound C=1C=CC=CC=1[Si](Cl)(C(C)(C)C)C1=CC=CC=C1 MHYGQXWCZAYSLJ-UHFFFAOYSA-N 0.000 claims description 4
125000000008 (C1-C10) alkyl group Chemical group 0.000 claims description 3
150000001721 carbon Chemical group 0.000 claims description 3
150000002085 enols Chemical class 0.000 claims description 3
125000001624 naphthyl group Chemical group 0.000 claims description 3
125000004433 nitrogen atom Chemical group N* 0.000 claims description 3
125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 2
MASDFXZJIDNRTR-UHFFFAOYSA-N 1,3-bis(trimethylsilyl)urea Chemical compound C[Si](C)(C)NC(=O)N[Si](C)(C)C MASDFXZJIDNRTR-UHFFFAOYSA-N 0.000 claims description 2
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 claims description 2
FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 claims description 2
YKFRUJSEPGHZFJ-UHFFFAOYSA-N N-trimethylsilylimidazole Chemical compound C[Si](C)(C)N1C=CN=C1 YKFRUJSEPGHZFJ-UHFFFAOYSA-N 0.000 claims description 2
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 2
WLLIXJBWWFGEHT-UHFFFAOYSA-N [tert-butyl(dimethyl)silyl] trifluoromethanesulfonate Chemical compound CC(C)(C)[Si](C)(C)OS(=O)(=O)C(F)(F)F WLLIXJBWWFGEHT-UHFFFAOYSA-N 0.000 claims description 2
VFFLZSQFWJXUJJ-UHFFFAOYSA-N bromo-tert-butyl-methoxy-phenylsilane Chemical compound CO[Si](Br)(C(C)(C)C)C1=CC=CC=C1 VFFLZSQFWJXUJJ-UHFFFAOYSA-N 0.000 claims description 2
MNKYQPOFRKPUAE-UHFFFAOYSA-N chloro(triphenyl)silane Chemical compound C=1C=CC=CC=1[Si](C=1C=CC=CC=1)(Cl)C1=CC=CC=C1 MNKYQPOFRKPUAE-UHFFFAOYSA-N 0.000 claims description 2
KWYZNESIGBQHJK-UHFFFAOYSA-N chloro-dimethyl-phenylsilane Chemical compound C[Si](C)(Cl)C1=CC=CC=C1 KWYZNESIGBQHJK-UHFFFAOYSA-N 0.000 claims description 2
125000004663 dialkyl amino group Chemical group 0.000 claims description 2
SBZXBUIDTXKZTM-UHFFFAOYSA-N diglyme Chemical compound COCCOCCOC SBZXBUIDTXKZTM-UHFFFAOYSA-N 0.000 claims description 2
QQFBQBDINHJDMN-UHFFFAOYSA-N ethyl 2-trimethylsilylacetate Chemical compound CCOC(=O)C[Si](C)(C)C QQFBQBDINHJDMN-UHFFFAOYSA-N 0.000 claims description 2
238000004519 manufacturing process Methods 0.000 claims description 2
125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 claims description 2
BSVDKGAOBFIKOB-UHFFFAOYSA-N n-tert-butyl-2,2,2-trifluoro-n-propan-2-ylacetamide Chemical compound CC(C)N(C(C)(C)C)C(=O)C(F)(F)F BSVDKGAOBFIKOB-UHFFFAOYSA-N 0.000 claims description 2
VUENSYJCBOSTCS-UHFFFAOYSA-N tert-butyl-imidazol-1-yl-dimethylsilane Chemical compound CC(C)(C)[Si](C)(C)N1C=CN=C1 VUENSYJCBOSTCS-UHFFFAOYSA-N 0.000 claims description 2
BCNZYOJHNLTNEZ-UHFFFAOYSA-N tert-butyldimethylsilyl chloride Chemical compound CC(C)(C)[Si](C)(C)Cl BCNZYOJHNLTNEZ-UHFFFAOYSA-N 0.000 claims description 2
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 2
STMPXDBGVJZCEX-UHFFFAOYSA-N triethylsilyl trifluoromethanesulfonate Chemical compound CC[Si](CC)(CC)OS(=O)(=O)C(F)(F)F STMPXDBGVJZCEX-UHFFFAOYSA-N 0.000 claims description 2
FTVLMFQEYACZNP-UHFFFAOYSA-N trimethylsilyl trifluoromethanesulfonate Chemical compound C[Si](C)(C)OS(=O)(=O)C(F)(F)F FTVLMFQEYACZNP-UHFFFAOYSA-N 0.000 claims description 2
239000008096 xylene Substances 0.000 claims description 2
125000002887 hydroxy group Chemical group [H]O* 0.000 claims 6
125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 2
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 claims 2
125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims 1
125000004705 ethylthio group Chemical group C(C)S* 0.000 claims 1
125000005000 thioaryl group Chemical group 0.000 claims 1
125000004432 carbon atom Chemical group C* 0.000 description 18
239000002253 acid Substances 0.000 description 13
229910052731 fluorine Inorganic materials 0.000 description 11
239000011737 fluorine Substances 0.000 description 11
125000004356 hydroxy functional group Chemical group O* 0.000 description 11
125000003282 alkyl amino group Chemical group 0.000 description 10
125000001188 haloalkyl group Chemical group 0.000 description 10
150000001336 alkenes Chemical class 0.000 description 9
238000003786 synthesis reaction Methods 0.000 description 9
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 8
230000015572 biosynthetic process Effects 0.000 description 8
238000006243 chemical reaction Methods 0.000 description 8
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 8
LISFMEBWQUVKPJ-UHFFFAOYSA-N quinolin-2-ol Chemical compound C1=CC=C2NC(=O)C=CC2=C1 LISFMEBWQUVKPJ-UHFFFAOYSA-N 0.000 description 8
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 7
125000004442 acylamino group Chemical group 0.000 description 7
150000001345 alkine derivatives Chemical class 0.000 description 7
125000004390 alkyl sulfonyl group Chemical group 0.000 description 7
230000000845 anti-microbial effect Effects 0.000 description 7
239000000460 chlorine Substances 0.000 description 7
229910052801 chlorine Inorganic materials 0.000 description 7
125000005553 heteroaryloxy group Chemical group 0.000 description 7
239000000543 intermediate Substances 0.000 description 7
125000002950 monocyclic group Chemical group 0.000 description 7
239000000243 solution Substances 0.000 description 7
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
125000002619 bicyclic group Chemical group 0.000 description 6
239000012458 free base Substances 0.000 description 6
125000001183 hydrocarbyl group Chemical group 0.000 description 6
239000002243 precursor Substances 0.000 description 6
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 5
230000000844 anti-bacterial effect Effects 0.000 description 5
125000001153 fluoro group Chemical group F* 0.000 description 5
239000000047 product Substances 0.000 description 5
238000010992 reflux Methods 0.000 description 5
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
229930194542 Keto Natural products 0.000 description 4
125000006580 bicyclic heterocycloalkyl group Chemical group 0.000 description 4
239000011203 carbon fibre reinforced carbon Substances 0.000 description 4
230000000694 effects Effects 0.000 description 4
125000000468 ketone group Chemical group 0.000 description 4
230000000670 limiting effect Effects 0.000 description 4
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 4
229920006395 saturated elastomer Polymers 0.000 description 4
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 3
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
241000124008 Mammalia Species 0.000 description 3
241001465754 Metazoa Species 0.000 description 3
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
125000002252 acyl group Chemical group 0.000 description 3
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 3
229910052794 bromium Inorganic materials 0.000 description 3
125000004122 cyclic group Chemical group 0.000 description 3
125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 3
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
229910052760 oxygen Inorganic materials 0.000 description 3
239000001301 oxygen Substances 0.000 description 3
239000011541 reaction mixture Substances 0.000 description 3
238000006884 silylation reaction Methods 0.000 description 3
239000007858 starting material Substances 0.000 description 3
239000000126 substance Substances 0.000 description 3
125000005323 thioketone group Chemical group 0.000 description 3
GBOBPUGNRIBKKL-UHFFFAOYSA-N 3,4-dimethoxy-4-nitrocyclohexa-1,5-diene-1-carboxylic acid Chemical compound COC1C=C(C(O)=O)C=CC1(OC)[N+]([O-])=O GBOBPUGNRIBKKL-UHFFFAOYSA-N 0.000 description 2
LWGCZCMLPRMKIZ-UHFFFAOYSA-N 4-fluoro-3-methoxybenzoic acid Chemical compound COC1=CC(C(O)=O)=CC=C1F LWGCZCMLPRMKIZ-UHFFFAOYSA-N 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
241000894006 Bacteria Species 0.000 description 2
HTJDQJBWANPRPF-UHFFFAOYSA-N Cyclopropylamine Chemical compound NC1CC1 HTJDQJBWANPRPF-UHFFFAOYSA-N 0.000 description 2
QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
241000282414 Homo sapiens Species 0.000 description 2
108700020474 Penicillin-Binding Proteins Proteins 0.000 description 2
XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 2
KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 2
YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 2
125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 description 2
150000007513 acids Chemical class 0.000 description 2
150000001252 acrylic acid derivatives Chemical class 0.000 description 2
125000004423 acyloxy group Chemical group 0.000 description 2
238000004458 analytical method Methods 0.000 description 2
125000000129 anionic group Chemical group 0.000 description 2
150000001450 anions Chemical class 0.000 description 2
239000003242 anti bacterial agent Substances 0.000 description 2
239000002259 anti human immunodeficiency virus agent Substances 0.000 description 2
229940124411 anti-hiv antiviral agent Drugs 0.000 description 2
150000007514 bases Chemical class 0.000 description 2
230000008901 benefit Effects 0.000 description 2
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
235000010233 benzoic acid Nutrition 0.000 description 2
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 2
150000001732 carboxylic acid derivatives Chemical class 0.000 description 2
125000002091 cationic group Chemical group 0.000 description 2
125000006575 electron-withdrawing group Chemical group 0.000 description 2
SYKMLRACELWIOH-UHFFFAOYSA-N ethyl 1-cyclopropyl-7-fluoro-8-methoxy-2-oxo-3,4-dihydroquinoline-3-carboxylate Chemical compound C(C)OC(=O)C1C(N(C2=C(C(=CC=C2C1)F)OC)C1CC1)=O SYKMLRACELWIOH-UHFFFAOYSA-N 0.000 description 2
238000001704 evaporation Methods 0.000 description 2
230000008020 evaporation Effects 0.000 description 2
238000001727 in vivo Methods 0.000 description 2
244000005700 microbiome Species 0.000 description 2
239000003960 organic solvent Substances 0.000 description 2
125000001181 organosilyl group Chemical group [SiH3]* 0.000 description 2
CTSLXHKWHWQRSH-UHFFFAOYSA-N oxalyl chloride Chemical compound ClC(=O)C(Cl)=O CTSLXHKWHWQRSH-UHFFFAOYSA-N 0.000 description 2
230000000144 pharmacologic effect Effects 0.000 description 2
125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 2
230000004260 plant-type cell wall biogenesis Effects 0.000 description 2
125000006239 protecting group Chemical group 0.000 description 2
239000000376 reactant Substances 0.000 description 2
229930195734 saturated hydrocarbon Natural products 0.000 description 2
229910052710 silicon Inorganic materials 0.000 description 2
239000010703 silicon Substances 0.000 description 2
229910000104 sodium hydride Inorganic materials 0.000 description 2
239000012312 sodium hydride Substances 0.000 description 2
239000012453 solvate Substances 0.000 description 2
125000003003 spiro group Chemical group 0.000 description 2
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
125000004641 (C1-C12) haloalkyl group Chemical group 0.000 description 1
125000004178 (C1-C4) alkyl group Chemical group 0.000 description 1
125000004191 (C1-C6) alkoxy group Chemical group 0.000 description 1
125000000171 (C1-C6) haloalkyl group Chemical group 0.000 description 1
125000006701 (C1-C7) alkyl group Chemical group 0.000 description 1
FLBAYUMRQUHISI-UHFFFAOYSA-N 1,8-naphthyridine Chemical compound N1=CC=CC2=CC=CN=C21 FLBAYUMRQUHISI-UHFFFAOYSA-N 0.000 description 1
WEPXLRANFJEOFZ-UHFFFAOYSA-N 2,3,4-trifluorobenzoic acid Chemical compound OC(=O)C1=CC=C(F)C(F)=C1F WEPXLRANFJEOFZ-UHFFFAOYSA-N 0.000 description 1
HZNQSWJZTWOTKM-UHFFFAOYSA-N 2,3,4-trimethoxybenzoic acid Chemical compound COC1=CC=C(C(O)=O)C(OC)=C1OC HZNQSWJZTWOTKM-UHFFFAOYSA-N 0.000 description 1
FODBVCSYJKNBLO-UHFFFAOYSA-N 2,3-dimethoxybenzoic acid Chemical compound COC1=CC=CC(C(O)=O)=C1OC FODBVCSYJKNBLO-UHFFFAOYSA-N 0.000 description 1
JQNBCSPQVSUBSR-UHFFFAOYSA-N 2,3-dimethoxybenzoyl chloride Chemical compound COC1=CC=CC(C(Cl)=O)=C1OC JQNBCSPQVSUBSR-UHFFFAOYSA-N 0.000 description 1
125000004215 2,4-difluorophenyl group Chemical group [H]C1=C([H])C(*)=C(F)C([H])=C1F 0.000 description 1
BSQLQMLFTHJVKS-UHFFFAOYSA-N 2-chloro-1,3-benzothiazole Chemical compound C1=CC=C2SC(Cl)=NC2=C1 BSQLQMLFTHJVKS-UHFFFAOYSA-N 0.000 description 1
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
LUZUNVVXMDSFAB-UHFFFAOYSA-N 3,4,5-trifluoro-2-methoxybenzoyl chloride Chemical compound COC1=C(F)C(F)=C(F)C=C1C(Cl)=O LUZUNVVXMDSFAB-UHFFFAOYSA-N 0.000 description 1
UWGNGMRARPTMQZ-UHFFFAOYSA-N 3-fluoro-2-methoxy-4-piperidin-1-ylbenzoic acid Chemical compound C1=C(C(O)=O)C(OC)=C(F)C(N2CCCCC2)=C1 UWGNGMRARPTMQZ-UHFFFAOYSA-N 0.000 description 1
XWNCIWHUOQWPTJ-UHFFFAOYSA-N 4-bromo-2,3-dimethoxybenzoic acid Chemical compound COC1=C(Br)C=CC(C(O)=O)=C1OC XWNCIWHUOQWPTJ-UHFFFAOYSA-N 0.000 description 1
MACVJOXZYJDSMO-UHFFFAOYSA-N 4-bromo-3,4-dimethoxycyclohexa-1,5-diene-1-carboxylic acid Chemical compound COC1C=C(C(O)=O)C=CC1(Br)OC MACVJOXZYJDSMO-UHFFFAOYSA-N 0.000 description 1
RSBXOVZBSUWTCT-UHFFFAOYSA-N 4-chloro-2-methoxy-5-nitrobenzoic acid Chemical compound COC1=CC(Cl)=C([N+]([O-])=O)C=C1C(O)=O RSBXOVZBSUWTCT-UHFFFAOYSA-N 0.000 description 1
OXDACUJNZQJKIE-UHFFFAOYSA-N 4-fluoro-2,3-dimethoxybenzoic acid Chemical compound COC1=C(F)C=CC(C(O)=O)=C1OC OXDACUJNZQJKIE-UHFFFAOYSA-N 0.000 description 1
GMDWTBFLQVDQHR-UHFFFAOYSA-N 4-fluoro-3-methoxy-2-methylbenzenecarbothioic s-acid Chemical compound COC1=C(C)C(C(O)=S)=CC=C1F GMDWTBFLQVDQHR-UHFFFAOYSA-N 0.000 description 1
TYKMPQKMADHJCI-UHFFFAOYSA-N 4-fluoro-3-methoxy-2-phenylbenzenecarbothioic s-acid Chemical compound COC1=C(F)C=CC(C(S)=O)=C1C1=CC=CC=C1 TYKMPQKMADHJCI-UHFFFAOYSA-N 0.000 description 1
125000002373 5 membered heterocyclic group Chemical group 0.000 description 1
KISJQBUVHAHZFD-UHFFFAOYSA-N 6-methoxy-1,3-benzodioxole-5-carboxylic acid Chemical compound C1=C(C(O)=O)C(OC)=CC2=C1OCO2 KISJQBUVHAHZFD-UHFFFAOYSA-N 0.000 description 1
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
239000005711 Benzoic acid Substances 0.000 description 1
FERIUCNNQQJTOY-UHFFFAOYSA-M Butyrate Chemical compound CCCC([O-])=O FERIUCNNQQJTOY-UHFFFAOYSA-M 0.000 description 1
FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Natural products CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 1
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
239000004215 Carbon black (E152) Substances 0.000 description 1
KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 1
FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 1
VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 description 1
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
JVTAAEKCZFNVCJ-UHFFFAOYSA-M Lactate Chemical compound CC(O)C([O-])=O JVTAAEKCZFNVCJ-UHFFFAOYSA-M 0.000 description 1
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
OFOBLEOULBTSOW-UHFFFAOYSA-L Malonate Chemical compound [O-]C(=O)CC([O-])=O OFOBLEOULBTSOW-UHFFFAOYSA-L 0.000 description 1
AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 1
229910002651 NO3 Inorganic materials 0.000 description 1
NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
ZCQWOFVYLHDMMC-UHFFFAOYSA-N Oxazole Chemical compound C1=COC=N1 ZCQWOFVYLHDMMC-UHFFFAOYSA-N 0.000 description 1
KYGZCKSPAKDVKC-UHFFFAOYSA-N Oxolinic acid Chemical compound C1=C2N(CC)C=C(C(O)=O)C(=O)C2=CC2=C1OCO2 KYGZCKSPAKDVKC-UHFFFAOYSA-N 0.000 description 1
229910019142 PO4 Inorganic materials 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
125000000066 S-methyl group Chemical group [H]C([H])([H])S* 0.000 description 1
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 description 1
DTQVDTLACAAQTR-UHFFFAOYSA-M Trifluoroacetate Chemical compound [O-]C(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-M 0.000 description 1
125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
230000002378 acidificating effect Effects 0.000 description 1
125000005041 acyloxyalkyl group Chemical group 0.000 description 1
WNLRTRBMVRJNCN-UHFFFAOYSA-L adipate(2-) Chemical compound [O-]C(=O)CCCCC([O-])=O WNLRTRBMVRJNCN-UHFFFAOYSA-L 0.000 description 1
229910052783 alkali metal Inorganic materials 0.000 description 1
229910052784 alkaline earth metal Inorganic materials 0.000 description 1
125000003342 alkenyl group Chemical group 0.000 description 1
125000004183 alkoxy alkyl group Chemical group 0.000 description 1
125000005907 alkyl ester group Chemical group 0.000 description 1
125000005336 allyloxy group Chemical group 0.000 description 1
125000000266 alpha-aminoacyl group Chemical group 0.000 description 1
230000036436 anti-hiv Effects 0.000 description 1
229940088710 antibiotic agent Drugs 0.000 description 1
239000004599 antimicrobial Substances 0.000 description 1
239000000010 aprotic solvent Substances 0.000 description 1
125000002029 aromatic hydrocarbon group Chemical group 0.000 description 1
239000002585 base Substances 0.000 description 1
230000009286 beneficial effect Effects 0.000 description 1
150000001559 benzoic acids Chemical class 0.000 description 1
125000002618 bicyclic heterocycle group Chemical group 0.000 description 1
230000003115 biocidal effect Effects 0.000 description 1
230000004071 biological effect Effects 0.000 description 1
239000012267 brine Substances 0.000 description 1
125000004369 butenyl group Chemical group C(=CCC)* 0.000 description 1
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000011575 calcium Substances 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
JSVCEVCSANKFDY-SFYZADRCSA-N carbacephem Chemical compound C1CC(C)=C(C(O)=O)N2C(=O)[C@@H](NC(=O)C)[C@H]21 JSVCEVCSANKFDY-SFYZADRCSA-N 0.000 description 1
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 1
150000007942 carboxylates Chemical class 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
210000004027 cell Anatomy 0.000 description 1
210000002421 cell wall Anatomy 0.000 description 1
150000001782 cephems Chemical class 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
HCAJEUSONLESMK-UHFFFAOYSA-N cyclohexylsulfamic acid Chemical compound OS(=O)(=O)NC1CCCCC1 HCAJEUSONLESMK-UHFFFAOYSA-N 0.000 description 1
125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 description 1
201000010099 disease Diseases 0.000 description 1
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
238000006073 displacement reaction Methods 0.000 description 1
MOTZDAYCYVMXPC-UHFFFAOYSA-N dodecyl hydrogen sulfate Chemical compound CCCCCCCCCCCCOS(O)(=O)=O MOTZDAYCYVMXPC-UHFFFAOYSA-N 0.000 description 1
229940043264 dodecyl sulfate Drugs 0.000 description 1
239000003814 drug Substances 0.000 description 1
229940079593 drug Drugs 0.000 description 1
238000003821 enantio-separation Methods 0.000 description 1
238000005516 engineering process Methods 0.000 description 1
UYMKPFRHYYNDTL-UHFFFAOYSA-N ethenamine Chemical class NC=C UYMKPFRHYYNDTL-UHFFFAOYSA-N 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
ABMRHKNJTSAXOE-UHFFFAOYSA-N ethyl 1-cyclopropyl-8-methoxy-4-oxoquinoline-3-carboxylate Chemical compound C12=C(OC)C=CC=C2C(=O)C(C(=O)OCC)=CN1C1CC1 ABMRHKNJTSAXOE-UHFFFAOYSA-N 0.000 description 1
SSAKJQKZGFTARQ-UHFFFAOYSA-N ethyl 1-cyclopropyl-8-methoxy-7-nitro-4-oxoquinoline-3-carboxylate Chemical compound C12=C(OC)C([N+]([O-])=O)=CC=C2C(=O)C(C(=O)OCC)=CN1C1CC1 SSAKJQKZGFTARQ-UHFFFAOYSA-N 0.000 description 1
JODDVGWNUWGSMG-UHFFFAOYSA-N ethyl 2-(dimethylamino)prop-2-enoate Chemical compound CCOC(=O)C(=C)N(C)C JODDVGWNUWGSMG-UHFFFAOYSA-N 0.000 description 1
BVRGWZKXGLOJFR-UHFFFAOYSA-N ethyl 8-bromo-1-ethyl-8-methoxy-2-oxo-4,7-dihydro-3H-quinoline-3-carboxylate Chemical compound C(C)OC(=O)C1C(N(C=2C(CC=CC2C1)(Br)OC)CC)=O BVRGWZKXGLOJFR-UHFFFAOYSA-N 0.000 description 1
125000004494 ethyl ester group Chemical group 0.000 description 1
238000009472 formulation Methods 0.000 description 1
125000002485 formyl group Chemical group [H]C(*)=O 0.000 description 1
JFCQEDHGNNZCLN-UHFFFAOYSA-N glutaric acid Chemical compound OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 1
150000004820 halides Chemical class 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical group 0.000 description 1
XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-M hydrogensulfate Chemical compound OS([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-M 0.000 description 1
150000002463 imidates Chemical class 0.000 description 1
230000001771 impaired effect Effects 0.000 description 1
208000015181 infectious disease Diseases 0.000 description 1
230000002401 inhibitory effect Effects 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
239000013067 intermediate product Substances 0.000 description 1
238000003402 intramolecular cyclocondensation reaction Methods 0.000 description 1
239000011630 iodine Substances 0.000 description 1
229910052740 iodine Inorganic materials 0.000 description 1
238000005342 ion exchange Methods 0.000 description 1
GJRQTCIYDGXPES-UHFFFAOYSA-N isobutyl acetate Chemical compound CC(C)COC(C)=O GJRQTCIYDGXPES-UHFFFAOYSA-N 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
150000003951 lactams Chemical class 0.000 description 1
239000011777 magnesium Substances 0.000 description 1
229910052749 magnesium Inorganic materials 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
230000010534 mechanism of action Effects 0.000 description 1
125000000250 methylamino group Chemical group [H]N(*)C([H])([H])[H] 0.000 description 1
230000000813 microbial effect Effects 0.000 description 1
239000011707 mineral Substances 0.000 description 1
125000002911 monocyclic heterocycle group Chemical group 0.000 description 1
125000006578 monocyclic heterocycloalkyl group Chemical group 0.000 description 1
231100000252 nontoxic Toxicity 0.000 description 1
230000003000 nontoxic effect Effects 0.000 description 1
150000007523 nucleic acids Chemical class 0.000 description 1
102000039446 nucleic acids Human genes 0.000 description 1
108020004707 nucleic acids Proteins 0.000 description 1
UUSIAGKDLDQMHS-UHFFFAOYSA-N o-(2-methylpropyl) ethanethioate Chemical compound CC(C)COC(C)=S UUSIAGKDLDQMHS-UHFFFAOYSA-N 0.000 description 1
QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
239000003921 oil Substances 0.000 description 1
238000005457 optimization Methods 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
235000005985 organic acids Nutrition 0.000 description 1
229960000321 oxolinic acid Drugs 0.000 description 1
125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 description 1
125000004430 oxygen atom Chemical group O* 0.000 description 1
229940055076 parasympathomimetics choline ester Drugs 0.000 description 1
HHXMXAQDOUCLDN-RXMQYKEDSA-N penem Chemical compound S1C=CN2C(=O)C[C@H]21 HHXMXAQDOUCLDN-RXMQYKEDSA-N 0.000 description 1
230000035699 permeability Effects 0.000 description 1
235000021317 phosphate Nutrition 0.000 description 1
150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
125000005633 phthalidyl group Chemical group 0.000 description 1
125000003386 piperidinyl group Chemical group 0.000 description 1
239000002798 polar solvent Substances 0.000 description 1
239000011591 potassium Substances 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
229940002612 prodrug Drugs 0.000 description 1
239000000651 prodrug Substances 0.000 description 1
125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
230000001681 protective effect Effects 0.000 description 1
238000001243 protein synthesis Methods 0.000 description 1
238000000746 purification Methods 0.000 description 1
125000005554 pyridyloxy group Chemical group 0.000 description 1
150000003248 quinolines Chemical class 0.000 description 1
230000002829 reductive effect Effects 0.000 description 1
230000008439 repair process Effects 0.000 description 1
238000000926 separation method Methods 0.000 description 1
125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
125000006850 spacer group Chemical group 0.000 description 1
238000003756 stirring Methods 0.000 description 1
125000005415 substituted alkoxy group Chemical group 0.000 description 1
239000000758 substrate Substances 0.000 description 1
KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 1
150000003871 sulfonates Chemical class 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
229940095064 tartrate Drugs 0.000 description 1
150000003892 tartrate salts Chemical class 0.000 description 1
229930192474 thiophene Natural products 0.000 description 1
JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
125000003944 tolyl group Chemical group 0.000 description 1
230000014616 translation Effects 0.000 description 1
125000004665 trialkylsilyl group Chemical group 0.000 description 1
ITMCEJHCFYSIIV-UHFFFAOYSA-M triflate Chemical compound [O-]S(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-M 0.000 description 1
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1
125000005023 xylyl group Chemical group 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- 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
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom 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
- C07D215/48—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
- C07D215/54—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen attached in position 3
- C07D215/56—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen attached in position 3 with oxygen atoms in position 4
- 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
- C07D401/04—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 directly linked by a ring-member-to-ring-member bond
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- 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
- C07D471/04—Ortho-condensed systems
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems

Landscapes

Organic Chemistry (AREA)
Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
General Health & Medical Sciences (AREA)
Public Health (AREA)
General Chemical & Material Sciences (AREA)
Medicinal Chemistry (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Pharmacology & Pharmacy (AREA)
Oncology (AREA)
Animal Behavior & Ethology (AREA)
Communicable Diseases (AREA)
Chemical Kinetics & Catalysis (AREA)
Veterinary Medicine (AREA)
Virology (AREA)
Tropical Medicine & Parasitology (AREA)
Molecular Biology (AREA)
AIDS & HIV (AREA)
Nitrogen Condensed Heterocyclic Rings (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Plural Heterocyclic Compounds (AREA)
Quinoline Compounds (AREA)
Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

NO20032667A 2000-12-14 2003-06-12 Cykliseringsfremgangsmatetrinn for fremstilling av kinoloner og naftyridiner NO325236B1 (no)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US25563300P	2000-12-14	2000-12-14
PCT/US2001/048536 WO2002048113A1 (en)	2000-12-14	2001-12-07	Cyclization process step in the making of quinolones and naphthyridines

Publications (3)

Publication Number	Publication Date
NO20032667D0 NO20032667D0 (no)	2003-06-12
NO20032667L NO20032667L (no)	2003-08-14
NO325236B1 true NO325236B1 (no)	2008-03-03

Family

ID=22969207

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO20032667A NO325236B1 (no)	2000-12-14	2003-06-12	Cykliseringsfremgangsmatetrinn for fremstilling av kinoloner og naftyridiner

Country Status (19)

Country	Link
EP (1)	EP1343766B1 (de)
JP (2)	JP4417007B2 (de)
KR (1)	KR100603163B1 (de)
CN (1)	CN1232508C (de)
AT (1)	ATE300522T1 (de)
AU (2)	AU2905702A (de)
BR (1)	BR0116229A (de)
CA (1)	CA2427831C (de)
CZ (1)	CZ20031379A3 (de)
DE (1)	DE60112325T2 (de)
DK (1)	DK1343766T3 (de)
ES (1)	ES2247190T3 (de)
HU (1)	HUP0303991A3 (de)
IL (2)	IL155677A0 (de)
MX (1)	MXPA03005338A (de)
NO (1)	NO325236B1 (de)
NZ (1)	NZ525569A (de)
PL (1)	PL207394B1 (de)
WO (1)	WO2002048113A1 (de)

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KR100735587B1 (ko) *	2002-08-05	2007-07-04	더 프록터 앤드 갬블 캄파니	퀴놀론계 항생제 중간체의 제조 방법
US6803469B2 (en) *	2002-08-05	2004-10-12	The Procter & Gamble Company	Process for preparing quinolone antibiotic intermediates
US7176220B2 (en)	2002-11-20	2007-02-13	Japan Tobacco Inc.	4-oxoquinoline compound and use thereof as pharmaceutical agent
US7402674B2 (en)	2004-01-31	2008-07-22	Sanofi-Aventis Deutschland Gmbh,	7-Phenylamino-4-quinolone-3-carboxylic acid derivatives, process for their preparation and their use as medicaments
JP4669040B2 (ja)	2006-03-06	2011-04-13	日本たばこ産業株式会社	４−オキソキノリン化合物の製造方法
CN101437801B (zh)	2006-03-06	2013-02-06	日本烟草产业株式会社	制备4-氧代喹啉化合物的方法
ES2536923T3 (es)	2006-09-12	2015-05-29	Gilead Sciences, Inc.	Proceso e intermedios para preparar inhibidores de la integrasa del VIH
US8658183B2 (en)	2007-08-09	2014-02-25	Taigen Biotechnology Company, Ltd.	Antimicrobial parenteral formulation
AR068403A1 (es)	2007-09-11	2009-11-18	Gilead Sciences Inc	Proceso e intermediarios para la preparacion de inhibidores de integrasa
AU2008358909B2 (en)	2008-07-01	2012-12-13	Taigen Biotechnology Co., Ltd.	Treatment of antibiotic-resistant bacteria infection
EP2880017B1 (de)	2012-08-03	2016-10-05	Gilead Sciences, Inc.	Verfahren und zwischenprodukte zur herstellung von integrase-hemmern
EP3824349A1 (de)	2018-07-19	2021-05-26	Lintfield Limited	Thioxanthonderivate, zusammensetzung damit und verfahren zur herstellung von mustern mit dieser zusammensetzung

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BR9508513A (pt) *	1994-08-02	1998-06-02	Procter & Gamble	Processo para a produção de antimicrobianos de quinolonil lactama e novos compostos intermediários
MX9700871A (es) *	1994-08-02	1997-05-31	Procter & Gamble	Procedimiento para hacer compuestos antimicrobianos.

2001
- 2001-12-07 HU HU0303991A patent/HUP0303991A3/hu unknown
- 2001-12-07 DK DK01990192T patent/DK1343766T3/da active
- 2001-12-07 CN CNB018207146A patent/CN1232508C/zh not_active Expired - Lifetime
- 2001-12-07 IL IL15567701A patent/IL155677A0/xx active IP Right Grant
- 2001-12-07 CZ CZ20031379A patent/CZ20031379A3/cs unknown
- 2001-12-07 KR KR1020037007905A patent/KR100603163B1/ko not_active Expired - Fee Related
- 2001-12-07 MX MXPA03005338A patent/MXPA03005338A/es active IP Right Grant
- 2001-12-07 NZ NZ525569A patent/NZ525569A/en not_active IP Right Cessation
- 2001-12-07 PL PL363355A patent/PL207394B1/pl not_active IP Right Cessation
- 2001-12-07 AU AU2905702A patent/AU2905702A/xx active Pending
- 2001-12-07 AT AT01990192T patent/ATE300522T1/de active
- 2001-12-07 ES ES01990192T patent/ES2247190T3/es not_active Expired - Lifetime
- 2001-12-07 BR BR0116229-2A patent/BR0116229A/pt not_active IP Right Cessation
- 2001-12-07 JP JP2002549644A patent/JP4417007B2/ja not_active Expired - Fee Related
- 2001-12-07 WO PCT/US2001/048536 patent/WO2002048113A1/en not_active Ceased
- 2001-12-07 EP EP01990192A patent/EP1343766B1/de not_active Expired - Lifetime
- 2001-12-07 CA CA002427831A patent/CA2427831C/en not_active Expired - Fee Related
- 2001-12-07 AU AU2002229057A patent/AU2002229057B2/en not_active Ceased
- 2001-12-07 DE DE60112325T patent/DE60112325T2/de not_active Expired - Lifetime
2003
- 2003-04-30 IL IL155677A patent/IL155677A/en not_active IP Right Cessation
- 2003-06-12 NO NO20032667A patent/NO325236B1/no not_active IP Right Cessation
2009
- 2009-10-05 JP JP2009231801A patent/JP2010001315A/ja not_active Withdrawn

Also Published As

Publication number	Publication date
KR20030063420A (ko)	2003-07-28
AU2905702A (en)	2002-06-24
EP1343766B1 (de)	2005-07-27
NO20032667D0 (no)	2003-06-12
DK1343766T3 (da)	2005-10-31
DE60112325T2 (de)	2006-05-24
IL155677A0 (en)	2003-11-23
CA2427831C (en)	2009-08-18
HUP0303991A3 (en)	2012-09-28
ES2247190T3 (es)	2006-03-01
JP2004515542A (ja)	2004-05-27
CN1481365A (zh)	2004-03-10
CZ20031379A3 (cs)	2003-11-12
KR100603163B1 (ko)	2006-07-24
NO20032667L (no)	2003-08-14
NZ525569A (en)	2004-09-24
PL207394B1 (pl)	2010-12-31
MXPA03005338A (es)	2003-10-06
JP2010001315A (ja)	2010-01-07
HUP0303991A2 (hu)	2004-04-28
AU2002229057B2 (en)	2005-04-21
ATE300522T1 (de)	2005-08-15
IL155677A (en)	2009-02-11
WO2002048113A1 (en)	2002-06-20
PL363355A1 (en)	2004-11-15
CN1232508C (zh)	2005-12-21
JP4417007B2 (ja)	2010-02-17
BR0116229A (pt)	2003-11-04
CA2427831A1 (en)	2002-06-20
EP1343766A1 (de)	2003-09-17
DE60112325D1 (de)	2005-09-01

Legal Events

Date	Code	Title	Description
2013-07-29	MM1K	Lapsed by not paying the annual fees

Publication	Publication Date	Title
JP2010001315A (ja)	2010-01-07	キノロン類及びナフチリジン類の製造方法における環化工程
KR100423778B1 (ko)	2004-03-24	항미생물성 퀴놀론, 그의 조성물 및 용도
EP1341781B1 (de)	2005-09-14	Antimikrobielle chinolone
AU2002230891A1 (en)	2002-08-29	Antimicrobial quinolones
MXPA05001180A (es)	2005-05-16	Derivados aza-biciclicos antimicrobianos, sus composiciones y usos.
AU2002229057A1 (en)	2002-08-29	Cyclization process step in the making of quinolones and naphthyridines
MC2262A1 (fr)	1993-04-26	Composes antibacteriens
KR100196440B1 (ko)	1999-06-15	항균제로서 유용한 7-치환-6-플루오로-1, 4-디하이드로-4-옥소-퀴놀린-3-카르복실산화합물
JP4094061B2 (ja)	2008-06-04	シス置換アミノシクロプロパン誘導体
AU2002230893B2 (en)	2005-06-09	Antimicrobial 2-pyridones, their compositions and uses
NZ233087A (en)	1991-07-26	(s)-7-(3-amino-1-pyrrolidinyl)-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-1,8 naphthyridine-3-carboxylic acid, esters, salts and pharmaceutical compositions
KR20010014209A (ko)	2001-02-26	시스-치환된 플루오로메틸피롤리딘 유도체
ES2232309A1 (es)	2005-05-16	Procedimiento simplificado para la obtencion de gatifloxacino.
KR100219327B1 (ko)	1999-09-01	퀴놀론 카르복실산 유도체
KR960001721B1 (ko)	1996-02-03	신규한 퀴놀론 카르복실산 유도체
KR100222083B1 (ko)	1999-10-01	7-(3-아미노메틸-4-벤질옥심) 피롤리딘 치환체를 갖는 신규 퀴놀린 카복실산 유도체
FR2625200A1 (en)	1989-06-30	7-(1-Azetidinyl)-1,4-dihydro-4-oxoquinoline-3-carboxylic acid derivatives, their preparation and their application as medicaments
WO2011091614A1 (zh)	2011-08-04	7-(2-取代-3-氨基-1-四氢吡咯[3，4-c]吡唑基)喹啉羧酸衍生物及其制备方法和在抗菌抗结核上的应用
MXPA00002649A (en)	2001-05-07	Antimicrobial quinolones, their compositions and uses