CN107001251A - 双(磺酰胺)衍生物及其作为mpges抑制剂的用途 - Google Patents

双(磺酰胺)衍生物及其作为mpges抑制剂的用途 Download PDF

Info

Publication number
CN107001251A
CN107001251A CN201580064771.XA CN201580064771A CN107001251A CN 107001251 A CN107001251 A CN 107001251A CN 201580064771 A CN201580064771 A CN 201580064771A CN 107001251 A CN107001251 A CN 107001251A
Authority
CN
China
Prior art keywords
compound
phenyl
formula
chloro
pharmaceutically acceptable
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.)
Pending
Application number
CN201580064771.XA
Other languages
English (en)
Chinese (zh)
Inventor
P·索德曼
M·斯文松
A·柯尔斯
L·欧博格
K·奥格丁
A·黑特曼
J·哈尔贝格
M·埃克
J·拜兰
J·努德
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Eike Doru M Real Estate Ltd
Original Assignee
Eike Doru M Real Estate Ltd
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
Application filed by Eike Doru M Real Estate Ltd filed Critical Eike Doru M Real Estate Ltd
Publication of CN107001251A publication Critical patent/CN107001251A/zh
Pending legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/30—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/37—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
    • C07C311/38—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring having sulfur atoms of sulfonamide groups and amino groups bound to carbon atoms of six-membered rings of the same carbon skeleton
    • C07C311/44—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring having sulfur atoms of sulfonamide groups and amino groups bound to carbon atoms of six-membered rings of the same carbon skeleton having the nitrogen atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • 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
    • A61K31/16—Amides, e.g. hydroxamic acids
    • A61K31/18—Sulfonamides
    • 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
    • A61K31/275—Nitriles; Isonitriles
    • A61K31/277—Nitriles; Isonitriles having a ring, e.g. verapamil
    • 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
    • A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
    • A61K31/404—Indoles, e.g. pindolol
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/30—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/37—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
    • C07C311/38—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring having sulfur atoms of sulfonamide groups and amino groups bound to carbon atoms of six-membered rings of the same carbon skeleton
    • C07C311/39—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring having sulfur atoms of sulfonamide groups and amino groups bound to carbon atoms of six-membered rings of the same carbon skeleton having the nitrogen atom of at least one of the sulfonamide groups bound to hydrogen atoms or to an acyclic carbon atom
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04—Indoles; Hydrogenated indoles
    • C07D209/08—Indoles; Hydrogenated indoles with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to carbon atoms of the hetero ring
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04—Indoles; Hydrogenated indoles
    • C07D209/30—Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
    • C07D209/32—Oxygen atoms
    • C07D209/34—Oxygen atoms in position 2

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Epidemiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Indole Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
CN201580064771.XA 2014-11-27 2015-11-24 双(磺酰胺)衍生物及其作为mpges抑制剂的用途 Pending CN107001251A (zh)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
SE1451434-3 2014-11-27
SE1451434 2014-11-27
PCT/SE2015/051261 WO2016085391A1 (en) 2014-11-27 2015-11-24 Bis(sulfonamide) derivatives and their use as mpges inhibitors

Publications (1)

Publication Number Publication Date
CN107001251A true CN107001251A (zh) 2017-08-01

Family

ID=56074770

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201580064771.XA Pending CN107001251A (zh) 2014-11-27 2015-11-24 双(磺酰胺)衍生物及其作为mpges抑制剂的用途

Country Status (5)

Country Link
US (1) US10227296B2 (https=)
EP (1) EP3224241A4 (https=)
JP (1) JP2017537157A (https=)
CN (1) CN107001251A (https=)
WO (1) WO2016085391A1 (https=)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SMT202000024T1 (it) * 2014-11-27 2020-03-13 Gesynta Pharma Ab Derivati di bis (solfonammide) e loro uso come inibitori di mpges

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20050250818A1 (en) * 2004-05-04 2005-11-10 Pfizer Inc Ortho substituted aryl or heteroaryl amide compounds
US20090131468A1 (en) * 2007-11-15 2009-05-21 Astrazeneca Ab Bis-(Sulfonylamino) Derivatives in Therapy 065
US20100292279A1 (en) * 2009-05-14 2010-11-18 Astrazeneca Ab Bis-(Sulfonylamino) Derivatives in Therapy
CN101945859A (zh) * 2007-12-20 2011-01-12 阿斯利康(瑞典)有限公司 用于治疗的二(磺酰基氨基)衍生物

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6211197B1 (en) * 1998-10-07 2001-04-03 Merck Frosst Canada & Co. Prostaglandin receptor ligands
CN101284773A (zh) * 2001-08-09 2008-10-15 小野药品工业株式会社 羧酸衍生物及以它为活性成分的药剂
CA2620363A1 (en) 2005-10-13 2007-04-19 Biolipox Ab Naphthalene-disulfonamides useful for the treatment of inflammation
WO2008129276A1 (en) 2007-04-19 2008-10-30 Boehringer Ingelheim International Gmbh Disulfonamides useful in the treatment of inflammation
WO2008129288A2 (en) 2007-04-19 2008-10-30 Boehringer Ingelheim International Gmbh Disulfonamides useful in the treatment of inflammation
TW200930369A (en) 2007-11-15 2009-07-16 Astrazeneca Ab Bis-(sulfonylamino) derivatives in therapy
CA2747835A1 (en) * 2009-01-19 2010-07-22 Abbott Laboratories Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20050250818A1 (en) * 2004-05-04 2005-11-10 Pfizer Inc Ortho substituted aryl or heteroaryl amide compounds
US20090131468A1 (en) * 2007-11-15 2009-05-21 Astrazeneca Ab Bis-(Sulfonylamino) Derivatives in Therapy 065
CN101945859A (zh) * 2007-12-20 2011-01-12 阿斯利康(瑞典)有限公司 用于治疗的二(磺酰基氨基)衍生物
US20100292279A1 (en) * 2009-05-14 2010-11-18 Astrazeneca Ab Bis-(Sulfonylamino) Derivatives in Therapy

Also Published As

Publication number Publication date
US20180002278A1 (en) 2018-01-04
JP2017537157A (ja) 2017-12-14
WO2016085391A1 (en) 2016-06-02
EP3224241A4 (en) 2018-08-08
EP3224241A1 (en) 2017-10-04
US10227296B2 (en) 2019-03-12

Similar Documents

Publication Publication Date Title
CN105828820B (zh) 布罗莫结构域抑制剂
JP5869740B2 (ja) Ｇａｂａａ受容体モジュレーターとしてのイミダゾピリダジン誘導体
ES2532357T3 (es) Derivados de sulfonamida como inhibidores de Nav1.7 para el tratamiento del dolor
TWI546289B (zh) 嗒酮化合物及其作為d-胺基酸氧化酶酵素(daao)抑制劑之用途
CN112218857B (zh) P300/cbp hat抑制剂及其使用方法
CN101160285A (zh) 适用于治疗疼痛的n-(n-磺酰氨基甲基)环丙烷甲酰胺衍生物
WO2023084158A1 (en) Cyp11a1 inhibitors
TW201022283A (en) Fused imidazole carboxamides as TRPV3 modulators
CN101506181B (zh) 三环化合物及其制药用途
CN101622233A (zh) 三环化合物及其药物用途
CN101687810A (zh) 双环化合物及其药物用途
EP3131893B1 (en) Polycyclic herg activators
ES2278980T3 (es) Derivados de 4'-metanosulfonil-bifenilo como un inhibidor muy selectivo de ciclooxigenasa-2.
US6809204B2 (en) Processes for the preparation of substituted isoxazoles and 2-isoxazolines
CN107001251A (zh) 双(磺酰胺)衍生物及其作为mpges抑制剂的用途
ES2349066T3 (es) Compuestos de piridilmetilbiciclocarboxamida sustituida.
JP6649538B2 (ja) ビス（スルホンアミド）誘導体およびｍＰＧＥＳ阻害薬としてのその使用

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
AD01 Patent right deemed abandoned

Effective date of abandoning: 20200310

AD01 Patent right deemed abandoned