HK1083341A1 - Stable crystal of 4-oxoquinoline compound - Google Patents

Stable crystal of 4-oxoquinoline compound

Info

Publication number
HK1083341A1
HK1083341A1 HK06105469.5A HK06105469A HK1083341A1 HK 1083341 A1 HK1083341 A1 HK 1083341A1 HK 06105469 A HK06105469 A HK 06105469A HK 1083341 A1 HK1083341 A1 HK 1083341A1
Authority
HK
Hong Kong
Prior art keywords
stable crystal
oxoquinoline compound
oxoquinoline
compound
crystal
Prior art date
Application number
HK06105469.5A
Other languages
English (en)
Inventor
Motohide Satoh
Takahisa Motomura
Takashi Matsuda
Kentaro Kondo
Koji Ando
Koji Matsuda
Shuji Miyake
Hideto Uehara
Original Assignee
Japan Tobacco Inc
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.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=35079161&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=HK1083341(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Japan Tobacco Inc filed Critical Japan Tobacco Inc
Publication of HK1083341A1 publication Critical patent/HK1083341A1/xx

Links

Classifications

    • 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/47—Quinolines; Isoquinolines
    • 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
    • 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

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Virology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Oncology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Communicable Diseases (AREA)
  • AIDS & HIV (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Molecular Biology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Quinoline Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
HK06105469.5A 2004-05-20 2006-05-11 Stable crystal of 4-oxoquinoline compound HK1083341A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2004150979 2004-05-20
PCT/JP2005/009604 WO2005113508A1 (en) 2004-05-20 2005-05-19 Stable crystal of 4-oxoquinoline compound

Publications (1)

Publication Number Publication Date
HK1083341A1 true HK1083341A1 (en) 2006-06-30

Family

ID=35079161

Family Applications (1)

Application Number Title Priority Date Filing Date
HK06105469.5A HK1083341A1 (en) 2004-05-20 2006-05-11 Stable crystal of 4-oxoquinoline compound

Country Status (32)

Country Link
US (6) US7635704B2 (sl)
EP (4) EP4299563A3 (sl)
JP (1) JP3754064B2 (sl)
KR (1) KR20080064909A (sl)
CN (1) CN1956961B (sl)
AR (2) AR049280A1 (sl)
AU (1) AU2005245296B2 (sl)
BR (1) BRPI0510114B8 (sl)
CA (1) CA2566922C (sl)
CY (1) CY1113010T1 (sl)
DK (2) DK3281939T3 (sl)
ES (2) ES2960824T3 (sl)
FI (2) FI3281939T3 (sl)
FR (1) FR23C1040I1 (sl)
HK (1) HK1083341A1 (sl)
HR (2) HRP20231588T3 (sl)
HU (2) HUE064615T2 (sl)
IL (1) IL179250A0 (sl)
LT (1) LT3281939T (sl)
MX (1) MXPA06013405A (sl)
MY (1) MY134672A (sl)
NO (6) NO339223B1 (sl)
NZ (1) NZ551839A (sl)
PE (2) PE20120361A1 (sl)
PL (2) PL3281939T3 (sl)
PT (2) PT1636190E (sl)
RS (2) RS52375B (sl)
RU (1) RU2330845C1 (sl)
SI (2) SI1636190T1 (sl)
TW (1) TWI329015B (sl)
WO (1) WO2005113508A1 (sl)
ZA (1) ZA200610647B (sl)

Families Citing this family (37)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6891227B2 (en) 2002-03-20 2005-05-10 International Business Machines Corporation Self-aligned nanotube field effect transistor and method of fabricating same
SK2662004A3 (sk) * 2002-11-20 2005-06-02 Japan Tobacco, Inc. Zlúčenina s obsahom 4-oxochinolínu a jej použitie ako inhibítora integráz
MY134672A (en) * 2004-05-20 2007-12-31 Japan Tobacco Inc Stable crystal of 4-oxoquinoline compound
WO2007063869A1 (ja) * 2005-11-30 2007-06-07 Japan Tobacco Inc. 高純度キノロン化合物の製造方法
AU2013203476C1 (en) * 2005-12-30 2016-11-17 Gilead Sciences, Inc. Methods for improving the pharmacokinetics of hiv integrase inhibitors
EA201201496A1 (ru) * 2005-12-30 2013-07-30 Джилид Сайэнс, Инк. Способ ингибирования интегразы вич, способ улучшения фармакокинетики 6-(3-хлор-2-фторбензил)-1-[(2s)-1-гидрокси-3-метилбутан-2-ил]-7-метокси-4-оксо-1,4-дигидрохинолин-3-карбоновой кислоты (варианты), набор, фармацевтическая композиция (варианты) и антиретровирусный агент (варианты)
US20090233964A1 (en) * 2005-12-30 2009-09-17 Gilead Sciences, Inc. Methods for improving the pharmacokinetics of hiv integrase inhibitors
JP2009525261A (ja) * 2006-02-01 2009-07-09 日本たばこ産業株式会社 レトロウイルス感染症の治療のための、６−（３−クロロ−２−フルオロベンジル）−１−［（２ｓ）−１−ヒドロキシ−３−メチルブタン−２−イル］−７−メトキシ−４−オキソ−１，４−ジヒドロキノリン−３−カルボン酸またはその塩の使用
WO2007092802A1 (en) * 2006-02-09 2007-08-16 Boehringer Ingelheim International Gmbh Method for treating hiv infection through co-administration of tipranavir and gs 9137
AP2914A (en) * 2006-03-06 2014-05-31 Japan Tobacco Inc Method for producing 4-oxoquinoline compound
WO2007102499A1 (ja) 2006-03-06 2007-09-13 Japan Tobacco Inc. ４－オキソキノリン化合物の製造方法
EA020489B1 (ru) 2006-07-07 2014-11-28 Джилид Сайэнс, Инк. Модуляторы фармакокинетических свойств лекарственных средств
WO2008033836A2 (en) 2006-09-12 2008-03-20 Gilead Sciences, Inc. Process and intermediates for preparing integrase inhibitors
SG183059A1 (en) * 2007-02-23 2012-08-30 Gilead Sciences Inc Modulators of pharmacokinetic properties of therapeutics
NZ582089A (en) * 2007-06-29 2013-01-25 Gilead Sciences Inc Antiviral Combination of elvitegravir, lopinavir and optionally ritonavir
AR067183A1 (es) * 2007-06-29 2009-09-30 Gilead Sciences Inc Composiciones terapeuticas y metodos, usos y equipos
AR068403A1 (es) * 2007-09-11 2009-11-18 Gilead Sciences Inc Proceso e intermediarios para la preparacion de inhibidores de integrasa
PL2296633T3 (pl) 2008-05-02 2016-03-31 Gilead Sciences Inc Zastosowanie cząsteczek stałych nośników dla udoskonalenia przetwarzalności środka farmaceutycznego
MX2011008289A (es) 2009-02-06 2011-09-15 Gilead Sciences Inc Tabletas para terapia combinada.
WO2010137032A2 (en) * 2009-05-14 2010-12-02 Matrix Laboratories Ltd. Novel polymorphic forms of elvitegravir and its pharmaceutically acceptable salts
WO2011004389A2 (en) * 2009-06-18 2011-01-13 Matrix Laboratories Ltd An improved process for the preparation of elvitegravir
CN102212032B (zh) * 2011-04-20 2013-07-31 复旦大学 一种5-羟基喹诺酮类衍生物及其制备方法和用途
EP2870138B1 (en) 2012-07-06 2018-08-22 Genentech, Inc. N-substituted benzamides and methods of use thereof
EP2880017B1 (en) 2012-08-03 2016-10-05 Gilead Sciences, Inc. Process and intermediates for preparing integrase inhibitors
CN103819402B (zh) * 2012-11-17 2016-03-30 上海迪赛诺化学制药有限公司 埃替拉韦中间体及其制备方法和应用
CN103864682B (zh) * 2012-12-18 2016-12-28 上海迪赛诺化学制药有限公司 一种制备iii型埃替拉韦晶体的方法
DK3067358T3 (da) 2012-12-21 2019-11-04 Gilead Sciences Inc Polycykliske carbamoylpyridon-forbindelser og deres farmaceutiske anvendelse
PT3019503T (pt) 2013-07-12 2017-11-27 Gilead Sciences Inc Compostos carbamoílpiridona- policíclicos e seu uso para o tratamento de infecções por hiv
NO2865735T3 (sl) 2013-07-12 2018-07-21
CN105315203A (zh) * 2014-06-06 2016-02-10 上海迪赛诺化学制药有限公司 一种v型埃替拉韦晶体及其制备方法
TWI744723B (zh) 2014-06-20 2021-11-01 美商基利科學股份有限公司 多環型胺甲醯基吡啶酮化合物之合成
NO2717902T3 (sl) 2014-06-20 2018-06-23
TW201613936A (en) 2014-06-20 2016-04-16 Gilead Sciences Inc Crystalline forms of(2R,5S,13aR)-8-hydroxy-7,9-dioxo-n-(2,4,6-trifluorobenzyl)-2,3,4,5,7,9,13,13a-octahydro-2,5-methanopyrido[1',2':4,5]pyrazino[2,1-b][1,3]oxazepine-10-carboxamide
TWI738321B (zh) 2014-12-23 2021-09-01 美商基利科學股份有限公司 多環胺甲醯基吡啶酮化合物及其醫藥用途
KR20190057158A (ko) 2015-04-02 2019-05-27 길리애드 사이언시즈, 인코포레이티드 폴리시클릭-카르바모일피리돈 화합물 및 그의 제약 용도
CN106008195B (zh) * 2016-05-19 2018-08-03 绍兴文理学院 一种2，4-二氟-5-碘苯甲酸的制备方法
EP3984536A1 (en) * 2020-10-19 2022-04-20 Centre national de la recherche scientifique Inhibition of the hiv-1 replication by compounds directed against a new target of the viral cycle

Family Cites Families (35)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3472859A (en) * 1966-11-01 1969-10-14 Sterling Drug Inc 1-alkyl-1,4-dihydro-4-oxo-3 quinoline-carboxylic acids and esters
JPS567162B1 (sl) 1970-09-14 1981-02-16
JPS4826772A (sl) 1971-08-11 1973-04-09
JPS6450979A (en) 1987-08-21 1989-02-27 Hitachi Shipbuilding Eng Co Method for discriminating whistle sound
JPH0651229B2 (ja) 1989-07-31 1994-07-06 新日本製鐵株式会社 プラズマアーク溶接方法および装置
IL100555A (en) 1991-02-07 2000-08-31 Hoechst Marion Roussel Inc N-substituted quinoline derivatives their preparation their use for the preparation of medicaments and the pharmaceutical compositions containing them
JP2993316B2 (ja) 1992-05-27 1999-12-20 宇部興産株式会社 アリール基又は複素芳香環基置換アミノキノロン誘導体及びエイズ治療剤
NO304832B1 (no) 1992-05-27 1999-02-22 Ube Industries Aminokinolonderivater samt middel mot HIV
JPH06199835A (ja) 1993-01-08 1994-07-19 Hokuriku Seiyaku Co Ltd ８−ジフルオロメトキシキノリン−３−カルボン酸誘導体
JPH06271568A (ja) 1993-03-22 1994-09-27 Hokuriku Seiyaku Co Ltd ７−フェニルピペラジニルキノリン−３−カルボン酸誘導体
JP2930539B2 (ja) 1994-07-18 1999-08-03 三共株式会社 トリフルオロメチルキノリンカルボン酸誘導体
RU2140919C1 (ru) 1994-07-18 1999-11-10 Убе Индастриз Лтд. Производные 8-трифторметилхинолинкарбоновой кислоты, фармацевтическая композиция и способ ингибирования вируса иммунодефицита
JPH0826772A (ja) 1994-07-22 1996-01-30 Sony Corp 融着用ガラス、その製造方法及び製造装置、並びに磁気ヘッドの製造方法
JP4121151B2 (ja) 1996-04-12 2008-07-23 アメリカ合衆国 抗新生物薬および抗レトロウイルス薬として有用なアクリドンから誘導された化合物
FR2761687B1 (fr) 1997-04-08 2000-09-15 Centre Nat Rech Scient Derives de quinoleines, possedant notamment des proprietes antivirales, leurs preparations et leurs applications biologiques
JP3776203B2 (ja) 1997-05-13 2006-05-17 第一製薬株式会社 Ｉｃａｍ−１産生阻害剤
GB9721964D0 (en) 1997-10-16 1997-12-17 Pfizer Ltd Isoquinolines
US6399629B1 (en) 1998-06-01 2002-06-04 Microcide Pharmaceuticals, Inc. Efflux pump inhibitors
US6248739B1 (en) 1999-01-08 2001-06-19 Pharmacia & Upjohn Company Quinolinecarboxamides as antiviral agents
US6248736B1 (en) 1999-01-08 2001-06-19 Pharmacia & Upjohn Company 4-oxo-1,4-dihydro-3-quinolinecarboxamides as antiviral agents
PE20011349A1 (es) 2000-06-16 2002-01-19 Upjohn Co 1-aril-4-oxo-1,4-dihidro-3-quinolincarboxamidas como agentes antivirales
US6559145B2 (en) 2000-07-12 2003-05-06 Pharmacia & Upjohn Company Heterocycle carboxamides as antiviral agents
US20050010048A1 (en) 2000-10-12 2005-01-13 Linghang Zhuang Aza-and polyaza-naphthalenly ketones useful as hiv integrase inhibitors
EP1326610B1 (en) 2000-10-12 2006-11-15 Merck & Co., Inc. Aza-and polyaza-naphthalenyl carboxamides useful as hiv integrase inhibitors
MXPA03007765A (es) 2001-03-01 2003-12-08 Shionogi & Co Compuestos heteroarilo que contienen nitrogeno, que tienen actividad inhibitoria contra virus de inmunodeficiencia humana integrasa.
JP2002293745A (ja) 2001-03-29 2002-10-09 St Marianna Univ School Of Medicine 慢性関節リウマチ治療剤
US20030138483A1 (en) * 2001-05-25 2003-07-24 Sergio Petriconi Soft elastic capsules and compositions thereof
US6627646B2 (en) * 2001-07-17 2003-09-30 Sepracor Inc. Norastemizole polymorphs
FR2827600A1 (fr) 2001-07-20 2003-01-24 Lipha Derives acides de quinolone et leurs applications en therapeutique
JP4035765B2 (ja) 2002-10-31 2008-01-23 横河電機株式会社 フーリエ変換型赤外線分光計
SK2662004A3 (sk) * 2002-11-20 2005-06-02 Japan Tobacco, Inc. Zlúčenina s obsahom 4-oxochinolínu a jej použitie ako inhibítora integráz
JP3567162B1 (ja) 2002-11-20 2004-09-22 日本たばこ産業株式会社 ４−オキソキノリン化合物及びそのｈｉｖインテグラーゼ阻害剤としての利用
MY134672A (en) * 2004-05-20 2007-12-31 Japan Tobacco Inc Stable crystal of 4-oxoquinoline compound
US7531554B2 (en) * 2004-05-20 2009-05-12 Japan Tobacco Inc. 4-oxoquinoline compound and use thereof as HIV integrase inhibitor
EP2332538A1 (en) 2004-05-21 2011-06-15 Japan Tobacco, Inc. Combinations comprising a 4-isoquinolone derivative and anti-HIV agents

Also Published As

Publication number Publication date
PL3281939T3 (pl) 2024-03-18
EP4299563A2 (en) 2024-01-03
EP4299563A3 (en) 2024-02-28
HUS2400006I1 (hu) 2024-04-28
RU2330845C1 (ru) 2008-08-10
JP2006001927A (ja) 2006-01-05
PE20060358A1 (es) 2006-05-12
NO20065790L (no) 2007-02-07
LT3281939T (lt) 2023-11-27
SI3281939T1 (sl) 2024-02-29
TWI329015B (en) 2010-08-21
US20100204271A1 (en) 2010-08-12
HRP20120681T1 (hr) 2012-09-30
US20190185433A1 (en) 2019-06-20
CA2566922C (en) 2011-01-11
NO20220690A1 (no) 2007-02-07
JP3754064B2 (ja) 2006-03-08
CN1956961A (zh) 2007-05-02
US20150361044A1 (en) 2015-12-17
HUE064615T2 (hu) 2024-04-28
EP3281939B1 (en) 2023-10-18
US20060030710A1 (en) 2006-02-09
FI3281939T3 (fi) 2023-10-23
ES2388441T3 (es) 2012-10-15
PT1636190E (pt) 2012-08-20
CN1956961B (zh) 2010-05-26
NO20161297A1 (no) 2007-02-07
US20220235009A1 (en) 2022-07-28
BRPI0510114B8 (pt) 2021-05-25
NO339223B1 (no) 2016-11-21
ES2960824T3 (es) 2024-03-06
ZA200610647B (en) 2008-06-25
SI1636190T1 (sl) 2012-09-28
FR23C1040I1 (fr) 2023-12-29
FIC20240008I1 (fi) 2024-03-20
CA2566922A1 (en) 2005-12-01
IL179250A0 (en) 2007-03-08
DK3281939T3 (da) 2024-01-22
RS64845B1 (sr) 2023-12-29
PT3281939T (pt) 2023-11-22
MXPA06013405A (es) 2007-03-01
BRPI0510114B1 (pt) 2020-09-15
DK1636190T3 (da) 2012-09-24
CY1113010T1 (el) 2016-04-13
KR20080064909A (ko) 2008-07-09
AU2005245296B2 (en) 2010-08-12
HRP20231588T3 (hr) 2024-03-15
NO20200873A1 (no) 2007-02-07
EP3281939A1 (en) 2018-02-14
EP1636190B1 (en) 2012-06-27
WO2005113508A1 (en) 2005-12-01
MY134672A (en) 2007-12-31
US7635704B2 (en) 2009-12-22
TW200600097A (en) 2006-01-01
US20180029989A1 (en) 2018-02-01
US8981103B2 (en) 2015-03-17
NO20230913A1 (no) 2007-02-07
EP2514746A1 (en) 2012-10-24
PE20120361A1 (es) 2012-05-03
AU2005245296A1 (en) 2005-12-01
RS52375B (en) 2012-12-31
NZ551839A (en) 2009-11-27
AR049280A1 (es) 2006-07-12
NO347902B1 (no) 2024-05-06
BRPI0510114A (pt) 2007-09-25
NO20190051A1 (no) 2007-02-07
EP1636190A1 (en) 2006-03-22
AR096100A2 (es) 2015-12-09
PL1636190T3 (pl) 2012-10-31

Similar Documents

Publication Publication Date Title
HUS2400006I1 (hu) Egy 4-oxokinolin-vegyület stabil kristályát tartalmazó kombináció
SI1802579T1 (sl) Derivati 3-arilaminopiridina
EP1756092A4 (en) NEW INHIBITORS OF RHO-KINASEN
PT1778618E (pt) Síntese de trietilenotetraminas
WO2007038678A8 (en) Analogs of ghrelin
EP1711484A4 (en) SYNTHESIS OF CYANOIMINO-BENZOIMIDAZOLES
HK1112710A1 (en) Reducing by-catch of seabirds
AU157195S (en) Watch
GB0410498D0 (en) Crystal
IL178184A0 (en) Synthesis of pyrrole-2-carbonitriles
GB0510501D0 (en) Display of operational instructions
AU158223S (en) Wristwatch
ZA200508325B (en) Manufacture of kerbstones
SI1709057T1 (sl) Sinteza spongozina
AU2004905330A0 (en) Construction of amahs
PL369353A1 (pl) Zestaw elementów budowlanych
GB0425577D0 (en) Single crystal scintillators
GB0423342D0 (en) Manufacture of amides
GB0406275D0 (en) Modification of seed
GB0415064D0 (en) Watch
HU2974U (en) Fluid-displaying watch
PL365717A1 (en) Forty percent solution of ammonal
GB0509729D0 (en) Selection of component
GB0412550D0 (en) Novel compound
GB0413757D0 (en) Novel compound