IN2014MN02467A - - Google Patents

Download PDF

Info

Publication number
IN2014MN02467A
IN2014MN02467A IN2467MUN2014A IN2014MN02467A IN 2014MN02467 A IN2014MN02467 A IN 2014MN02467A IN 2467MUN2014 A IN2467MUN2014 A IN 2467MUN2014A IN 2014MN02467 A IN2014MN02467 A IN 2014MN02467A
Authority
IN
India
Prior art keywords
tetrahydrothieno
thiazol
dioxo
pyrimidin
difluoro
Prior art date
Application number
Other languages
English (en)
Inventor
Suresh Mahadev Kadam
Abraham Thomas
Sukumar Sinha
Sukeerthi Kumar
Bipin Parsottam Kansagra
Sachin Gavhane
Sandeep Bandu Khandagale
Shailesh Pawase
Jayant Prakashrao Patil
Shailendra Bhadane
Bhavna Mishra
Rajesh Dwivedi
Original Assignee
Glenmark Pharmaceuticals Sa
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=54193746&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=IN2014MN02467(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Glenmark Pharmaceuticals Sa filed Critical Glenmark Pharmaceuticals Sa
Priority to IN2467MUN2014 priority Critical patent/IN2014MN02467A/en
Publication of IN2014MN02467A publication Critical patent/IN2014MN02467A/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D495/00Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
    • C07D495/02Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D495/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/46Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/52Two oxygen atoms
    • C07D239/54Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy radicals
    • C07D239/545Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy radicals with other hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/553Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy radicals with other hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms with halogen atoms or nitro radicals directly attached to ring carbon atoms, e.g. fluorouracil
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/46Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/60Three or more oxygen or sulfur atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/13Crystalline forms, e.g. polymorphs
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/29Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
    • Y10T428/2982Particulate matter [e.g., sphere, flake, etc.]

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
IN2467MUN2014 2012-06-08 2013-06-08 IN2014MN02467A (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
IN2467MUN2014 IN2014MN02467A (fr) 2012-06-08 2013-06-08

Applications Claiming Priority (6)

Application Number Priority Date Filing Date Title
IN1687MU2012 2012-06-08
US201261665282P 2012-06-27 2012-06-27
IN3519MU2012 2012-12-13
US201261748016P 2012-12-31 2012-12-31
PCT/IB2013/054703 WO2013183035A2 (fr) 2012-06-08 2013-06-08 Amides de composés de 2-amino-4-arylthiazole et leurs sels
IN2467MUN2014 IN2014MN02467A (fr) 2012-06-08 2013-06-08

Publications (1)

Publication Number Publication Date
IN2014MN02467A true IN2014MN02467A (fr) 2015-07-10

Family

ID=54193746

Family Applications (1)

Application Number Title Priority Date Filing Date
IN2467MUN2014 IN2014MN02467A (fr) 2012-06-08 2013-06-08

Country Status (22)

Country Link
US (1) US9458173B2 (fr)
EP (1) EP2858999B1 (fr)
JP (1) JP5989900B2 (fr)
KR (1) KR20150015488A (fr)
CN (1) CN104350058A (fr)
AP (1) AP3546A (fr)
AU (1) AU2013273118B2 (fr)
BR (1) BR112014029155A2 (fr)
CA (1) CA2873570C (fr)
CL (1) CL2014003317A1 (fr)
EA (1) EA031334B1 (fr)
HK (1) HK1207643A1 (fr)
IL (1) IL236084A0 (fr)
IN (1) IN2014MN02467A (fr)
MX (1) MX354014B (fr)
MY (1) MY165622A (fr)
NZ (1) NZ701721A (fr)
PE (1) PE20142306A1 (fr)
PH (1) PH12014502685A1 (fr)
SG (1) SG11201408093PA (fr)
WO (1) WO2013183035A2 (fr)
ZA (1) ZA201500082B (fr)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20150040265A (ko) 2012-06-08 2015-04-14 길리애드 사이언시즈, 인코포레이티드 플라비비리대 바이러스의 마크로시클릭 저해제
AR091279A1 (es) 2012-06-08 2015-01-21 Gilead Sciences Inc Inhibidores macrociclicos de virus flaviviridae
EP3010489A1 (fr) 2013-06-20 2016-04-27 Glenmark Pharmaceuticals S.A. Formulation nanoparticulaire comprenant un antagoniste de trpa1
WO2016023832A1 (fr) * 2014-08-11 2016-02-18 Hydra Biosciences, Inc. Dérivés de thiéno- et furo[2,3-d]pyrimidine-2,4(1h,3h)-dione à titre de modulateurs des trpc5 pour le traitement des troubles neuropsychiatriques
WO2016042501A1 (fr) * 2014-09-16 2016-03-24 Glenmark Pharmaceuticals S.A. Antagoniste de trpa1 permettant le traitement de la douleur associée à la douleur neuropathique diabétique
TW202321229A (zh) 2021-08-18 2023-06-01 美商富曼西公司 殺真菌的取代的雜環化合物
CN114671875A (zh) * 2022-04-27 2022-06-28 成都施贝康生物医药科技有限公司 新型二氢嘧啶类化合物、异构体或盐及其制备方法和用途

Family Cites Families (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2248231A1 (de) 1972-10-02 1974-04-11 Basf Ag 3-aminoisothiazolo eckige klammer auf 3,4-d eckige klammer zu pyrimidine
SE9701398D0 (sv) 1997-04-15 1997-04-15 Astra Pharma Prod Novel compounds
ES2193839B1 (es) * 2001-06-22 2005-02-16 Almirall Prodesfarma, S.A. Nuevos derivados de 6-fenildihidropirrolpirimidindiona.
AU2003253165A1 (en) * 2002-08-13 2004-02-25 Warner-Lambert Company Llc Pyrimidine fused bicyclic metalloproteinase inhibitors
US6890923B2 (en) 2002-12-16 2005-05-10 Astrazeneca Ab Compounds
AU2003290066A1 (en) 2002-12-18 2004-07-09 Novartis Ag Anktm1, a cold-activated trp-like channel expressed in nociceptive neurons
EP1657238A4 (fr) 2003-08-22 2008-12-03 Takeda Pharmaceutical Derive de pyrimidine fusionne et utilisation associee
US20070099940A1 (en) 2004-02-11 2007-05-03 Spearing Paul K Pth agonists
WO2005089206A2 (fr) 2004-03-13 2005-09-29 Irm Llc Modulateurs du canal ionique trpa1
JPWO2006083005A1 (ja) 2005-02-03 2008-06-26 武田薬品工業株式会社 縮合ピリミジン誘導体およびその用途
WO2007019251A2 (fr) 2005-08-04 2007-02-15 Apogee Biotechnology Corporation Inhibiteurs de la sphingosine kinase et leurs methodes d'utilisation
US20070105920A1 (en) 2005-11-08 2007-05-10 Akzo Nobel N.V. 2-(Benzimidazol-1-Yl)-N-(4-phenylthiazol-2-yl) acetamide derivatives
CN102499921A (zh) * 2005-12-22 2012-06-20 海德拉生物科学公司 治疗疼痛的方法和组合物
CN101454318A (zh) * 2006-03-22 2009-06-10 阿斯利康(瑞典)有限公司 吡啶并嘧啶衍生物及其作为pde4抑制剂的用途
TW200800997A (en) 2006-03-22 2008-01-01 Astrazeneca Ab Chemical compounds
JP2011201776A (ja) 2008-07-23 2011-10-13 Mochida Pharmaceut Co Ltd ヘテロシクリデン−n−(3,4−ジヒドロ−2(1h)−キナゾリノン−5−イル)アセトアミド誘導体
AR065081A1 (es) 2007-01-29 2009-05-13 Xenon Pharmaceuticals Inc Compuestos de quinazolinona y pirimidona fusionados y composicion farmaceutica
US8163761B2 (en) * 2007-06-22 2012-04-24 Hydra Biosciences, Inc. Methods and compositions for treating disorders
US7951814B2 (en) * 2008-06-17 2011-05-31 Glenmark Pharmaceuticals, S.A. Quinazolinedione derivatives as TRPA1 modulators
WO2009158719A2 (fr) 2008-06-27 2009-12-30 Hydra Biosciences, Inc. Méthodes et compositions de traitement de troubles
EA201190191A1 (ru) 2009-03-23 2012-11-30 Гленмарк Фармасьютикалс, С.А. Изотиазоло-пиримидинедионовые производные в качестве модуляторов trpa1
US8623880B2 (en) 2009-03-23 2014-01-07 Glenmark Pharmaceuticals S.A. Fused pyrimidine-dione derivatives as TRPA1 modulators
KR20110128898A (ko) 2009-03-23 2011-11-30 그렌마크 파머수티칼스 에스. 아. Trpa1 조절자로서 푸로피리미딘디온 유도체
JP5657638B2 (ja) 2009-03-23 2015-01-21 グレンマーク ファーマシューティカルズ, エセ.アー. Trpa1調節因子としての縮合ピリミジンジオン誘導体
EA023141B1 (ru) 2010-12-20 2016-04-29 Гленмарк Фармасьютикалс С.А. Соединения 2-амино-4-арилтиазола в качестве антагонистов trpa1

Also Published As

Publication number Publication date
CA2873570A1 (fr) 2013-12-12
PH12014502685B1 (en) 2015-01-26
US20150111038A1 (en) 2015-04-23
PE20142306A1 (es) 2015-01-16
IL236084A0 (en) 2015-02-01
US9458173B2 (en) 2016-10-04
NZ701721A (en) 2016-03-31
AP3546A (en) 2016-01-14
AP2014008076A0 (en) 2014-11-30
EP2858999A2 (fr) 2015-04-15
EP2858999B1 (fr) 2017-05-10
SG11201408093PA (en) 2015-01-29
KR20150015488A (ko) 2015-02-10
EA201492054A1 (ru) 2016-08-31
AU2013273118A1 (en) 2014-11-27
ZA201500082B (en) 2015-12-23
WO2013183035A2 (fr) 2013-12-12
MY165622A (en) 2018-04-18
AU2013273118B2 (en) 2015-11-05
JP5989900B2 (ja) 2016-09-07
PH12014502685A1 (en) 2015-01-26
MX354014B (es) 2018-02-08
MX2014014482A (es) 2015-06-05
JP2015520183A (ja) 2015-07-16
EA031334B1 (ru) 2018-12-28
CL2014003317A1 (es) 2015-02-13
CA2873570C (fr) 2016-11-01
HK1207643A1 (en) 2016-02-05
BR112014029155A2 (pt) 2017-06-27
WO2013183035A3 (fr) 2014-02-27
CN104350058A (zh) 2015-02-11

Similar Documents

Publication Publication Date Title
IN2014MN02467A (fr)
MY161757A (en) Meglumine salt of 6-fluoro-3-hydroxy-2-pyrazine carboxamide
PH12015501649A1 (en) Sodium salt of 6-fluoro-3-hydroxy-2-pyrazine carboxamide
CO6831982A2 (es) Pirazolo[4,3-d]pirimidinas útiles como inhibidores de cinasas
PH12012502138B1 (en) N3-substituted-n1-sulfonyl-5-fluoropyrimidinone derivatives
NZ749557A (en) 3-alkyl-5-fluoro-4-substituted-imino-3,4-dihydropyrimidin-2(1h)-one derivatives as fungicides
PH12016500250A1 (en) Novel triazolo [4,5-d] pyrimidine derivatives
EP2788000A4 (fr) Pyrrolopyrimidines en tant qu'inhibiteurs de kinase janus
ZA201306719B (en) 3,4-dihydro-pyrrolo[1,2-a]pyrazin-1-ylamine derivatives useful as inhibitors of beta-secretase (bace)
MY171831A (en) Novel fused pyrimidine compound or salt thereof
EP2938616A4 (fr) Procédé de préparation de tofacitinib et d'intermédiaires
MX2013015308A (es) Inhibidores de proteasoma y procesos para su preparacion, purificacion y uso.
PH12015500363A1 (en) Prodrugs of amino quinazoline kinase inhibitor
NZ701933A (en) Phenoxyethyl piperidine compounds
EA201591105A1 (ru) ПИРИМИДО[4,5-b]ХИНОЛИН-4,5-(3H,10H)-ДИОНЫ В КАЧЕСТВЕ СУПРЕССОРОВ НОНСЕНС МУТАЦИЙ
MX344911B (es) Compuestos de eter amido-piridilico y composiciones y su uso contra parasitos.
PH12015502409B1 (en) Pyrrolo[2,3-d]pyrimidine derivatives as cb2 receptor agonists
MX2014010423A (es) Sales de arginina utiles inmunologicamente.
GEP20146183B (en) Process for preparation of l-arginine salt of perindopril
EP2759529A4 (fr) Procédé de préparation de 1-palmitoyl-3-acétylglycérol et procédé de préparation de 1-palmitoyl-2-linoléoyl-3-acétylglycérol l'utilisant
EP2702044A4 (fr) Procédé de préparation de rilpivirine
WO2014160177A3 (fr) Inhibiteurs quinazolines de pi3k
EP2885302A4 (fr) Procédé de préparation d'inhibiteurs de dipeptidylpeptidase
CR20140545A (es) Piperazino[1,2-a]indol-1-onas y [1,4]diazepino [1,2-a]indol-1-ona
MY164134A (en) Carboxylic acid derivatives having an oxazolo[5,4-d]pyrimidine ring