JP2010526130A5 - - Google Patents
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- JP2010526130A5 JP2010526130A5 JP2010507014A JP2010507014A JP2010526130A5 JP 2010526130 A5 JP2010526130 A5 JP 2010526130A5 JP 2010507014 A JP2010507014 A JP 2010507014A JP 2010507014 A JP2010507014 A JP 2010507014A JP 2010526130 A5 JP2010526130 A5 JP 2010526130A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- alkoxy
- cycloalkyl
- hydroxyl
- halo
- 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.)
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- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 17
- 150000001875 compounds Chemical class 0.000 claims 17
- 125000000217 alkyl group Chemical group 0.000 claims 16
- 150000003839 salts Chemical class 0.000 claims 16
- -1 amino, hydroxyl Chemical group 0.000 claims 14
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 14
- 125000003545 alkoxy group Chemical group 0.000 claims 13
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims 12
- 229910052736 halogen Inorganic materials 0.000 claims 12
- 150000002367 halogens Chemical class 0.000 claims 12
- 125000000753 cycloalkyl group Chemical group 0.000 claims 10
- 229910052739 hydrogen Inorganic materials 0.000 claims 10
- 239000001257 hydrogen Substances 0.000 claims 10
- 229910052757 nitrogen Inorganic materials 0.000 claims 10
- 125000004093 cyano group Chemical group *C#N 0.000 claims 9
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims 9
- 125000005843 halogen group Chemical group 0.000 claims 8
- 150000002431 hydrogen Chemical class 0.000 claims 8
- 150000001204 N-oxides Chemical class 0.000 claims 7
- 125000001072 heteroaryl group Chemical group 0.000 claims 7
- 150000001735 carboxylic acids Chemical class 0.000 claims 6
- 239000000651 prodrug Substances 0.000 claims 6
- 229940002612 prodrug Drugs 0.000 claims 6
- 125000000041 C6-C10 aryl group Chemical group 0.000 claims 5
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims 5
- 125000006376 (C3-C10) cycloalkyl group Chemical group 0.000 claims 4
- 125000003118 aryl group Chemical group 0.000 claims 4
- 125000004104 aryloxy group Chemical group 0.000 claims 4
- 125000004122 cyclic group Chemical group 0.000 claims 4
- 125000000000 cycloalkoxy group Chemical group 0.000 claims 4
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 4
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 claims 3
- 125000006719 (C6-C10) aryl (C1-C6) alkyl group Chemical group 0.000 claims 3
- 125000004423 acyloxy group Chemical group 0.000 claims 3
- 125000004429 atom Chemical group 0.000 claims 3
- 125000002619 bicyclic group Chemical group 0.000 claims 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 3
- 125000001153 fluoro group Chemical group F* 0.000 claims 3
- 239000008194 pharmaceutical composition Substances 0.000 claims 3
- 239000012453 solvate Substances 0.000 claims 3
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims 2
- 125000004211 3,5-difluorophenyl group Chemical group [H]C1=C(F)C([H])=C(*)C([H])=C1F 0.000 claims 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 2
- 125000002252 acyl group Chemical group 0.000 claims 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 2
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 claims 2
- 125000004414 alkyl thio group Chemical group 0.000 claims 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 2
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 2
- 239000003085 diluting agent Substances 0.000 claims 2
- 239000003937 drug carrier Substances 0.000 claims 2
- 125000005553 heteroaryloxy group Chemical group 0.000 claims 2
- 125000005842 heteroatom Chemical group 0.000 claims 2
- 238000004519 manufacturing process Methods 0.000 claims 2
- 125000002950 monocyclic group Chemical group 0.000 claims 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 2
- 229910052760 oxygen Inorganic materials 0.000 claims 2
- 239000001301 oxygen Chemical group 0.000 claims 2
- 239000000546 pharmaceutical excipient Substances 0.000 claims 2
- 229910052717 sulfur Chemical group 0.000 claims 2
- 239000011593 sulfur Chemical group 0.000 claims 2
- 125000003396 thiol group Chemical class [H]S* 0.000 claims 2
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 2
- 239000003981 vehicle Substances 0.000 claims 2
- XILBJBALCLVHMC-HYFKYTBRSA-N (3r,4r)-1-[3-(2,5-difluorophenyl)cyclobutyl]-4-[(3s)-3-(3-fluoro-6-methoxyquinolin-4-yl)-3-hydroxypropyl]piperidine-3-carboxylic acid Chemical compound C([C@H]([C@H](C1)C(O)=O)CC[C@H](O)C2=C(F)C=NC3=CC=C(C=C32)OC)CN1C(C1)CC1C1=CC(F)=CC=C1F XILBJBALCLVHMC-HYFKYTBRSA-N 0.000 claims 1
- CXKTZIIMLVMOEE-LFTIPEMBSA-N (3r,4r)-1-[3-(2,5-difluorophenyl)cyclobutyl]-4-[3-(3-fluoro-6-methoxy-1,5-naphthyridin-4-yl)-3-hydroxypropyl]piperidine-3-carboxylic acid Chemical compound C([C@H]([C@H](C1)C(O)=O)CCC(O)C2=C(F)C=NC3=CC=C(N=C32)OC)CN1C(C1)CC1C1=CC(F)=CC=C1F CXKTZIIMLVMOEE-LFTIPEMBSA-N 0.000 claims 1
- ZZEFVGNVSJWANE-DLHRMPCLSA-N (3r,4r)-1-[3-(2,6-difluorophenyl)cyclobutyl]-4-[3-(3-fluoro-6-methoxy-1,5-naphthyridin-4-yl)-3-hydroxypropyl]piperidine-3-carboxylic acid Chemical compound C([C@H]([C@H](C1)C(O)=O)CCC(O)C2=C(F)C=NC3=CC=C(N=C32)OC)CN1C(C1)CC1C1=C(F)C=CC=C1F ZZEFVGNVSJWANE-DLHRMPCLSA-N 0.000 claims 1
- FZLRGYMRPZHZOB-SBNFKLEUSA-N (3r,4r)-1-[3-(2,6-difluorophenyl)cyclobutyl]-4-[3-hydroxy-3-(6-methoxyquinolin-4-yl)propyl]piperidine-3-carboxylic acid Chemical compound C([C@H]([C@H](C1)C(O)=O)CCC(O)C2=CC=NC3=CC=C(C=C32)OC)CN1C(C1)CC1C1=C(F)C=CC=C1F FZLRGYMRPZHZOB-SBNFKLEUSA-N 0.000 claims 1
- BFTYXXYZLWZEGV-BPZQULEUSA-N (3r,4r)-1-[3-(3,5-difluorophenyl)cyclobutyl]-4-[(3s)-3-(3-fluoro-6-methoxyquinolin-4-yl)-3-hydroxypropyl]piperidine-3-carboxylic acid Chemical compound C([C@H]([C@H](C1)C(O)=O)CC[C@H](O)C2=C(F)C=NC3=CC=C(C=C32)OC)CN1C(C1)CC1C1=CC(F)=CC(F)=C1 BFTYXXYZLWZEGV-BPZQULEUSA-N 0.000 claims 1
- ODCDHYIGRDDZIS-QLBQJLTJSA-N (3r,4r)-4-[3-(3-chloro-6-methoxyquinolin-4-yl)-3-hydroxypropyl]-1-(3-phenylcyclobutyl)piperidine-3-carboxylic acid Chemical compound C([C@H]([C@H](C1)C(O)=O)CCC(O)C2=C(Cl)C=NC3=CC=C(C=C32)OC)CN1C(C1)CC1C1=CC=CC=C1 ODCDHYIGRDDZIS-QLBQJLTJSA-N 0.000 claims 1
- NKOZTUDLFMCVOC-QLBQJLTJSA-N (3r,4r)-4-[3-(3-fluoro-6-methoxyquinolin-4-yl)-3-hydroxypropyl]-1-(3-phenylcyclobutyl)piperidine-3-carboxylic acid Chemical compound C([C@H]([C@H](C1)C(O)=O)CCC(O)C2=C(F)C=NC3=CC=C(C=C32)OC)CN1C(C1)CC1C1=CC=CC=C1 NKOZTUDLFMCVOC-QLBQJLTJSA-N 0.000 claims 1
- VSLZNKFMVLGHTG-JLYNRWRGSA-N (3r,4r)-4-[3-hydroxy-3-(6-methoxyquinolin-4-yl)propyl]-1-(3-phenylcyclobutyl)piperidine-3-carboxylic acid Chemical compound C([C@H]([C@H](C1)C(O)=O)CCC(O)C2=CC=NC3=CC=C(C=C32)OC)CN1C(C1)CC1C1=CC=CC=C1 VSLZNKFMVLGHTG-JLYNRWRGSA-N 0.000 claims 1
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 claims 1
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 claims 1
- HMKCREDERPZPTH-UHFFFAOYSA-N 3-[3-(3-chloro-6-methoxyquinolin-4-yl)propyl]-1-[3-(2,5-difluorophenyl)cyclobutyl]pyrrolidine-3-carboxylic acid Chemical compound C12=CC(OC)=CC=C2N=CC(Cl)=C1CCCC(C1)(C(O)=O)CCN1C(C1)CC1C1=CC(F)=CC=C1F HMKCREDERPZPTH-UHFFFAOYSA-N 0.000 claims 1
- 125000001054 5 membered carbocyclic group Chemical group 0.000 claims 1
- 208000035143 Bacterial infection Diseases 0.000 claims 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims 1
- 241000124008 Mammalia Species 0.000 claims 1
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 claims 1
- 125000005035 acylthio group Chemical group 0.000 claims 1
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims 1
- 125000004644 alkyl sulfinyl group Chemical group 0.000 claims 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims 1
- 208000022362 bacterial infectious disease Diseases 0.000 claims 1
- 125000001246 bromo group Chemical group Br* 0.000 claims 1
- 125000001309 chloro group Chemical group Cl* 0.000 claims 1
- 125000005170 cycloalkyloxycarbonyl group Chemical group 0.000 claims 1
- 125000005366 cycloalkylthio group Chemical group 0.000 claims 1
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 claims 1
- 239000003814 drug Substances 0.000 claims 1
- 125000004785 fluoromethoxy group Chemical group [H]C([H])(F)O* 0.000 claims 1
- 125000004216 fluoromethyl group Chemical group [H]C([H])(F)* 0.000 claims 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims 1
- 125000004470 heterocyclooxy group Chemical group 0.000 claims 1
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 claims 1
- 125000002346 iodo group Chemical group I* 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 229920006395 saturated elastomer Polymers 0.000 claims 1
- 150000003536 tetrazoles Chemical class 0.000 claims 1
- 229940124597 therapeutic agent Drugs 0.000 claims 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 claims 1
- ITMCEJHCFYSIIV-UHFFFAOYSA-M triflate Chemical compound [O-]S(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-M 0.000 claims 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US91690607P | 2007-05-09 | 2007-05-09 | |
| PCT/IB2008/001076 WO2008139288A2 (en) | 2007-05-09 | 2008-04-29 | Substituted heterocyclic derivatives and compositions and their pharmaceutical use as antibacterials |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2010526130A JP2010526130A (ja) | 2010-07-29 |
| JP2010526130A5 true JP2010526130A5 (OSRAM) | 2011-05-19 |
Family
ID=39865577
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010507014A Withdrawn JP2010526130A (ja) | 2007-05-09 | 2008-04-29 | 置換ヘテロ環式誘導体ならびにそれらの医薬使用および組成物 |
Country Status (17)
| Country | Link |
|---|---|
| US (3) | US20080280879A1 (OSRAM) |
| EP (2) | EP2481735A1 (OSRAM) |
| JP (1) | JP2010526130A (OSRAM) |
| KR (2) | KR20090130347A (OSRAM) |
| CN (1) | CN101679357A (OSRAM) |
| AR (1) | AR066478A1 (OSRAM) |
| AU (1) | AU2008249745B2 (OSRAM) |
| CA (1) | CA2685888A1 (OSRAM) |
| CL (1) | CL2008001367A1 (OSRAM) |
| IL (1) | IL201830A0 (OSRAM) |
| MX (1) | MX2009012117A (OSRAM) |
| PA (1) | PA8779801A1 (OSRAM) |
| PE (1) | PE20090240A1 (OSRAM) |
| TW (1) | TW200902518A (OSRAM) |
| UY (1) | UY31071A1 (OSRAM) |
| WO (1) | WO2008139288A2 (OSRAM) |
| ZA (1) | ZA200907761B (OSRAM) |
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2012532834A (ja) * | 2009-07-11 | 2012-12-20 | バイエル ファーマ アクチエンゲゼルシャフト | シクロアルキル基を用いる放射性標識方法 |
| MA41169A (fr) | 2014-12-17 | 2017-10-24 | Acraf | Composés antibactériens à large spectre d'activité |
| BR112018075297A2 (pt) | 2016-06-08 | 2019-03-19 | Aziende Chimiche Riunite Angelini Francesco A.C.R.A.F. S.P.A | composto, composição farmacêutica, e, método para tratar uma infecção bacteriana |
| JP6755775B2 (ja) * | 2016-11-04 | 2020-09-16 | 富士アミドケミカル株式会社 | ４−フルオロイソキノリンの製法 |
| CN112147257B (zh) * | 2017-03-24 | 2022-06-03 | 上海安谱实验科技股份有限公司 | Pet制品中多环芳烃的提取方法 |
| EP3732166A4 (en) * | 2017-12-26 | 2021-09-01 | Cytokinetics, Incorporated | PROCESS FOR THE PREPARATION OF AN AMINO-PYRIMIDINE AND ITS INTERMEDIARIES |
| CA3118752A1 (en) * | 2018-11-09 | 2020-05-14 | Vivace Therapeutics, Inc. | Bicyclic compounds |
| ES3014444T3 (en) | 2019-04-16 | 2025-04-22 | Vivace Therapeutics Inc | Bicyclic compounds |
| CN111848423B (zh) * | 2019-04-30 | 2022-10-14 | 尚科生物医药（上海）有限公司 | 3-氧代环丁基氨基甲酸叔丁酯的制备方法 |
| WO2021257863A1 (en) | 2020-06-19 | 2021-12-23 | Incyte Corporation | Pyrrolotriazine compounds as jak2 v617f inhibitors |
| WO2021257857A1 (en) | 2020-06-19 | 2021-12-23 | Incyte Corporation | Naphthyridinone compounds as jak2 v617f inhibitors |
| US11767323B2 (en) | 2020-07-02 | 2023-09-26 | Incyte Corporation | Tricyclic pyridone compounds as JAK2 V617F inhibitors |
| WO2022006457A1 (en) | 2020-07-02 | 2022-01-06 | Incyte Corporation | Tricyclic urea compounds as jak2 v617f inhibitors |
| WO2022046989A1 (en) | 2020-08-27 | 2022-03-03 | Incyte Corporation | Tricyclic urea compounds as jak2 v617f inhibitors |
| US11919908B2 (en) | 2020-12-21 | 2024-03-05 | Incyte Corporation | Substituted pyrrolo[2,3-d]pyrimidine compounds as JAK2 V617F inhibitors |
| WO2022182839A1 (en) | 2021-02-25 | 2022-09-01 | Incyte Corporation | Spirocyclic lactams as jak2 v617f inhibitors |
| CA3237199A1 (en) | 2021-11-02 | 2023-05-11 | Flare Therapeutics Inc. | Pparg inverse agonists and uses thereof |
| JP2025509672A (ja) | 2022-03-17 | 2025-04-11 | インサイト・コーポレイション | Ｊａｋ２ ｖ６１７ｆ阻害剤としての三環式尿素化合物 |
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2008
- 2008-04-29 CA CA002685888A patent/CA2685888A1/en not_active Abandoned
- 2008-04-29 KR KR1020097025640A patent/KR20090130347A/ko not_active Ceased
- 2008-04-29 KR KR1020127000612A patent/KR20120011093A/ko not_active Withdrawn
- 2008-04-29 EP EP12165102A patent/EP2481735A1/en not_active Withdrawn
- 2008-04-29 WO PCT/IB2008/001076 patent/WO2008139288A2/en not_active Ceased
- 2008-04-29 JP JP2010507014A patent/JP2010526130A/ja not_active Withdrawn
- 2008-04-29 EP EP08737576A patent/EP2155716A2/en not_active Withdrawn
- 2008-04-29 CN CN200880020428A patent/CN101679357A/zh active Pending
- 2008-04-29 MX MX2009012117A patent/MX2009012117A/es not_active Application Discontinuation
- 2008-04-29 AU AU2008249745A patent/AU2008249745B2/en not_active Ceased
- 2008-05-07 AR ARP080101937A patent/AR066478A1/es not_active Application Discontinuation
- 2008-05-07 PE PE2008000800A patent/PE20090240A1/es not_active Application Discontinuation
- 2008-05-08 TW TW097117046A patent/TW200902518A/zh unknown
- 2008-05-08 US US12/117,071 patent/US20080280879A1/en not_active Abandoned
- 2008-05-08 UY UY31071A patent/UY31071A1/es not_active Application Discontinuation
- 2008-05-09 PA PA20088779801A patent/PA8779801A1/es unknown
- 2008-05-09 CL CL2008001367A patent/CL2008001367A1/es unknown
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2009
- 2009-10-29 IL IL201830A patent/IL201830A0/en unknown
- 2009-11-04 ZA ZA200907761A patent/ZA200907761B/xx unknown
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2010
- 2010-12-20 US US12/972,620 patent/US20110092480A1/en not_active Abandoned
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2011
- 2011-11-22 US US13/302,151 patent/US20120065188A1/en not_active Abandoned