CN102718689A - 作为β淀粉样肽产生的抑制剂的新型α-(N-磺酰氨基)乙酰胺化合物 - Google Patents

作为β淀粉样肽产生的抑制剂的新型α-(N-磺酰氨基)乙酰胺化合物 Download PDF

Info

Publication number
CN102718689A
CN102718689A CN201210178082XA CN201210178082A CN102718689A CN 102718689 A CN102718689 A CN 102718689A CN 201210178082X A CN201210178082X A CN 201210178082XA CN 201210178082 A CN201210178082 A CN 201210178082A CN 102718689 A CN102718689 A CN 102718689A
Authority
CN
China
Prior art keywords
phenyl
compound
fluoro
amino
trifluoro
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
CN201210178082XA
Other languages
English (en)
Chinese (zh)
Inventor
J·E·小斯塔雷特
K·W·吉尔曼
R·E·奥尔森
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.)
Bristol Myers Squibb Co
Original Assignee
Bristol Myers Squibb Co
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=40193955&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=CN102718689(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Bristol Myers Squibb Co filed Critical Bristol Myers Squibb Co
Publication of CN102718689A publication Critical patent/CN102718689A/zh
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C311/00Amides 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
    • C07C311/15Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings
    • C07C311/16Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to hydrogen atoms or to an acyclic carbon atom
    • C07C311/19Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to hydrogen atoms or to an acyclic carbon atom to an acyclic carbon atom of a hydrocarbon radical substituted by carboxyl groups
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C237/00Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
    • C07C237/02Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton
    • C07C237/04Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being acyclic and saturated
    • C07C237/06Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being acyclic and saturated having the nitrogen atoms of the carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C253/00Preparation of carboxylic acid nitriles
    • C07C253/30Preparation of carboxylic acid nitriles by reactions not involving the formation of cyano groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D271/00Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms
    • C07D271/02Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms not condensed with other rings
    • C07D271/061,2,4-Oxadiazoles; Hydrogenated 1,2,4-oxadiazoles
    • 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/582Recycling of unreacted starting or intermediate materials

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Veterinary Medicine (AREA)
  • Hospice & Palliative Care (AREA)
  • Psychiatry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
CN201210178082XA 2007-10-31 2008-10-14 作为β淀粉样肽产生的抑制剂的新型α-(N-磺酰氨基)乙酰胺化合物 Pending CN102718689A (zh)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US98411807P 2007-10-31 2007-10-31
US60/984,118 2007-10-31

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
CN2008801240109A Division CN101910141B (zh) 2007-10-31 2008-10-14 作为β淀粉样肽产生的抑制剂的α-(N-磺酰氨基)乙酰胺化合物

Publications (1)

Publication Number Publication Date
CN102718689A true CN102718689A (zh) 2012-10-10

Family

ID=40193955

Family Applications (2)

Application Number Title Priority Date Filing Date
CN201210178082XA Pending CN102718689A (zh) 2007-10-31 2008-10-14 作为β淀粉样肽产生的抑制剂的新型α-(N-磺酰氨基)乙酰胺化合物
CN2008801240109A Expired - Fee Related CN101910141B (zh) 2007-10-31 2008-10-14 作为β淀粉样肽产生的抑制剂的α-(N-磺酰氨基)乙酰胺化合物

Family Applications After (1)

Application Number Title Priority Date Filing Date
CN2008801240109A Expired - Fee Related CN101910141B (zh) 2007-10-31 2008-10-14 作为β淀粉样肽产生的抑制剂的α-(N-磺酰氨基)乙酰胺化合物

Country Status (28)

Country Link
US (2) US8084477B2 (https=)
EP (3) EP2205575B1 (https=)
JP (1) JP5460605B2 (https=)
KR (1) KR20100075575A (https=)
CN (2) CN102718689A (https=)
AR (1) AR069135A1 (https=)
AT (1) ATE502022T1 (https=)
AU (1) AU2008319122A1 (https=)
BR (1) BRPI0818837A2 (https=)
CA (1) CA2704360A1 (https=)
CL (1) CL2008003271A1 (https=)
CO (1) CO6270332A2 (https=)
CY (2) CY1112337T1 (https=)
DE (1) DE602008005636D1 (https=)
DK (2) DK2295417T3 (https=)
EA (2) EA201171439A1 (https=)
ES (2) ES2390042T3 (https=)
HR (2) HRP20110219T1 (https=)
IL (1) IL205406A0 (https=)
MX (1) MX2010004319A (https=)
NZ (1) NZ584545A (https=)
PE (1) PE20091394A1 (https=)
PL (2) PL2205575T3 (https=)
PT (2) PT2205575E (https=)
SG (2) SG174043A1 (https=)
SI (2) SI2205575T1 (https=)
TW (1) TW200927099A (https=)
WO (1) WO2009058552A1 (https=)

Families Citing this family (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2471099C (en) 2001-12-20 2011-04-12 Bristol-Myers Squibb Company .alpha.-(n-sulphonamido)acetamide derivatives as .beta.-amyloid inhibitors
US8093276B2 (en) * 2007-10-31 2012-01-10 Bristol-Myers Squibb Company Alpha-(N-sulfonamido)acetamide compound as an inhibitor of beta amyloid peptide production
US8044077B2 (en) 2009-03-19 2011-10-25 Bristol-Myers Squibb Company Alpha-(N-sulfonamido)acetamide compounds incorporating deuterium as inhibitors of beta amyloid peptide production
CN102438622A (zh) * 2009-03-19 2012-05-02 百时美施贵宝公司 作为β淀粉样肽产生抑制剂的新颖α-(N-磺酰氨基)乙酰胺化合物
US7977362B2 (en) 2009-03-20 2011-07-12 Bristol-Myers Squibb Company Alpha-(N-benzenesulfonamido)cycloalkyl derivatives
US8252821B2 (en) * 2009-04-14 2012-08-28 Bristol-Myers Squibb Company Bioavailable capsule compositions of amorphous alpha-(N-sulfonamido)acetamide compound
TW201043269A (en) * 2009-04-14 2010-12-16 Bristol Myers Squibb Co Bioavailable compositions of amorphous alpha-(N-sulfonamido)acetamide compound
AU2011225122B8 (en) 2010-03-12 2013-12-12 Nippon Soda Co., Ltd. Compound containing pyridine ring and method for producing halogenated picoline derivative and tetrazolyloxime derivative
WO2012040444A2 (en) * 2010-09-24 2012-03-29 Bristol-Myers Squibb Company Treatment of patients with incipient alzheimer's disease
EP2643299B1 (en) 2010-11-22 2016-06-22 Noscira, S.A. Bipyridine sulfonamide derivatives for the treatment of neurodegenerative diseases or conditions
CN104797569A (zh) 2012-09-21 2015-07-22 百时美施贵宝公司 取代的1,5-苯并二氮杂*酮化合物
WO2014047370A1 (en) 2012-09-21 2014-03-27 Bristol-Myers Squibb Company Fluoroalkyl dibenzodiazepinone compounds
WO2014047392A1 (en) 2012-09-21 2014-03-27 Bristol-Myers Squibb Company Fluoroalkyl-1,4-benzodiazepinone compounds
CN104797584A (zh) 2012-09-21 2015-07-22 百时美施贵宝公司 作为notch抑制剂的三环杂环化合物
CN103058913B (zh) * 2012-12-13 2015-09-30 江苏弘和药物研发有限公司 5-氯异吲哚酮的合成方法
CN104163784B (zh) * 2014-06-20 2019-01-08 湖南天地恒一制药有限公司 一种奥拉西坦的合成工艺
WO2018111926A2 (en) 2016-12-16 2018-06-21 Inception 3, Inc. Methods of treating cochlear synaptopathy
US20200179511A1 (en) 2017-04-28 2020-06-11 Novartis Ag Bcma-targeting agent, and combination therapy with a gamma secretase inhibitor
EP3615055A1 (en) 2017-04-28 2020-03-04 Novartis AG Cells expressing a bcma-targeting chimeric antigen receptor, and combination therapy with a gamma secretase inhibitor
CN107935957B (zh) * 2017-12-02 2020-08-21 江苏仁明生物科技有限公司 一种合成高纯度沙坦侧链ttbb的方法
KR102870868B1 (ko) 2018-06-01 2025-10-15 노파르티스 아게 Bcma에 대한 결합 분자 및 이의 용도
CN108640886A (zh) * 2018-08-01 2018-10-12 余锋 一种作为β-淀粉样肽产生的抑制剂BMS-708163的合成方法
CN119679936A (zh) 2019-06-24 2025-03-25 诺华股份有限公司 针对靶向b细胞成熟抗原的多特异性抗体的给药方案和组合疗法
CN113466367B (zh) * 2021-06-25 2023-04-14 深圳万乐药业有限公司 乌苯美司原料药中α-苯乙胺杂质检测方法
CN113816874B (zh) * 2021-10-30 2024-01-26 大连双硼医药化工有限公司 一种合成4-氰基-2-氟苄醇的工艺方法

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH11343279A (ja) * 1998-03-16 1999-12-14 Shionogi & Co Ltd スルホンアミド誘導体およびそれらを含有するTNF―α産生抑制剤
CN1348442A (zh) * 1999-02-26 2002-05-08 默克公司 新的磺胺化合物及其应用
WO2003053912A1 (en) * 2001-12-20 2003-07-03 Bristol-Myers Squibb Company α-(N-SULPHONAMIDO)ACETAMIDE DERIVATIVES AS β-AMYLOID INHIBITORS

Family Cites Families (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5274094A (en) * 1990-08-15 1993-12-28 British Bio-Technology Limited Production of heterobicyclic containing benzene sulfonamides
GB9202791D0 (en) * 1992-02-11 1992-03-25 British Bio Technology Compounds
US5849736A (en) * 1993-11-24 1998-12-15 The Dupont Merck Pharmaceutical Company Isoxazoline and isoxazole fibrinogen receptor antagonists
SK282833B6 (sk) * 1995-11-17 2002-12-03 Warner-Lambert Company Sulfónamidové inhibítory matricových metaloproteináz a farmaceutická kompozícia obsahujúca tieto inhibítory
JP2000515153A (ja) 1996-07-22 2000-11-14 モンサント カンパニー チオールスルホンアミド メタロプロテアーゼインヒビター
US6313123B1 (en) * 1999-01-27 2001-11-06 American Cyanamid Company Acetylenic sulfonamide thiol tace inhibitors
AU766192B2 (en) 1999-01-27 2003-10-09 Wyeth Holdings Corporation Acetylenic sulfonamide thiol tace inhibitors
US6541467B1 (en) * 2000-04-14 2003-04-01 Corvas International, Inc. Thrombin inhibitors having a lactam at P3
US20020115640A1 (en) * 2000-11-30 2002-08-22 Claiborne Akiyo K. Farnesyltransferase inhibitors
IL159140A0 (en) * 2001-12-14 2004-06-01 Raytheon Co Precisely aligned lens structure and a method for its fabrication
CN1653064A (zh) * 2002-02-28 2005-08-10 阿斯特拉曾尼卡有限公司 噁唑烷酮衍生物、其制备方法以及包含它们的药用组合物
ES2286345T3 (es) * 2003-03-20 2007-12-01 Santhera Pharmaceuticals (Schweiz) Ag Derivados de piperidina y piperazina substituidos como moduladores del receptor de melanocortina-4.
KR20060002908A (ko) * 2003-03-31 2006-01-09 와이어쓰 베타 아밀로이드 생산 억제제인 플루오로- 및트리플루오로알킬-함유 헤테로사이클릭 설폰아미드 및 이의유도체
US7144894B2 (en) * 2004-09-23 2006-12-05 Bristol-Myers Squibb Company Sulfonamide bicyclic compounds
EP1984321A1 (en) * 2006-02-17 2008-10-29 Wyeth Methods for preparing sulfonamide substituted alcohols and intermediates thereof
AR059517A1 (es) * 2006-02-17 2008-04-09 Wyeth Corp N- sulfonilacion selectiva de alcoholes sustituidos con 2- aminotrifluoralquilo
WO2008112249A1 (en) 2007-03-13 2008-09-18 Trustees Of Columbia University In The City Of New York Synergistic interaction of notch-1 inhibitors with glucocorticoids
WO2009005688A2 (en) 2007-06-29 2009-01-08 Trustees Of Columbia University In The City Of New York Activating mutations in notch-1
US8093276B2 (en) 2007-10-31 2012-01-10 Bristol-Myers Squibb Company Alpha-(N-sulfonamido)acetamide compound as an inhibitor of beta amyloid peptide production
US8044077B2 (en) * 2009-03-19 2011-10-25 Bristol-Myers Squibb Company Alpha-(N-sulfonamido)acetamide compounds incorporating deuterium as inhibitors of beta amyloid peptide production

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH11343279A (ja) * 1998-03-16 1999-12-14 Shionogi & Co Ltd スルホンアミド誘導体およびそれらを含有するTNF―α産生抑制剤
CN1348442A (zh) * 1999-02-26 2002-05-08 默克公司 新的磺胺化合物及其应用
WO2003053912A1 (en) * 2001-12-20 2003-07-03 Bristol-Myers Squibb Company α-(N-SULPHONAMIDO)ACETAMIDE DERIVATIVES AS β-AMYLOID INHIBITORS

Also Published As

Publication number Publication date
TW200927099A (en) 2009-07-01
CY1112337T1 (el) 2015-12-09
US8350084B2 (en) 2013-01-08
AU2008319122A1 (en) 2009-05-07
HRP20110219T1 (hr) 2011-04-30
MX2010004319A (es) 2010-04-30
JP5460605B2 (ja) 2014-04-02
PE20091394A1 (es) 2009-09-25
KR20100075575A (ko) 2010-07-02
EP2205575B1 (en) 2011-03-16
WO2009058552A1 (en) 2009-05-07
CO6270332A2 (es) 2011-04-20
CN101910141B (zh) 2012-12-19
BRPI0818837A2 (pt) 2015-04-22
SI2205575T1 (sl) 2011-07-29
ATE502022T1 (de) 2011-04-15
US8084477B2 (en) 2011-12-27
JP2011502153A (ja) 2011-01-20
AR069135A1 (es) 2009-12-30
DK2205575T3 (da) 2011-07-11
SG174043A1 (en) 2011-09-29
PL2295417T3 (pl) 2012-11-30
DE602008005636D1 (de) 2011-04-28
CA2704360A1 (en) 2009-05-07
EP2295417B1 (en) 2012-07-04
EP2295417A1 (en) 2011-03-16
EA201000714A1 (ru) 2010-10-29
EA016447B1 (ru) 2012-05-30
HK1155161A1 (en) 2012-05-11
CN101910141A (zh) 2010-12-08
CY1113346T1 (el) 2016-06-22
CL2008003271A1 (es) 2009-07-10
EP2471769A1 (en) 2012-07-04
IL205406A0 (en) 2010-12-30
EA201171439A1 (ru) 2012-05-30
US20120088925A1 (en) 2012-04-12
NZ584545A (en) 2011-04-29
SG174044A1 (en) 2011-09-29
US20090111858A1 (en) 2009-04-30
PL2205575T3 (pl) 2011-09-30
EP2205575A1 (en) 2010-07-14
PT2295417E (pt) 2012-09-26
SI2295417T1 (sl) 2012-11-30
HK1141801A1 (en) 2010-11-19
DK2295417T3 (da) 2012-10-15
HRP20120703T1 (hr) 2012-09-30
ES2390042T3 (es) 2012-11-06
PT2205575E (pt) 2011-05-23
ES2361283T3 (es) 2011-06-15

Similar Documents

Publication Publication Date Title
CN102718689A (zh) 作为β淀粉样肽产生的抑制剂的新型α-(N-磺酰氨基)乙酰胺化合物
TWI398438B (zh) 作為雄性激素受體調節劑之四氫環戊〔b〕吲哚化合物
CN114760994A (zh) HIF-2α的抑制剂
NO332991B1 (no) Kalsiumreseptormodulerende forbindelse, farmasoytisk sammensetning og anvendelse derav
JP2018528246A (ja) Tead転写因子自己パルミトイル化阻害剤
CA2843853A1 (en) Macrocyclic insulin-degrading enzyme (ide) inhibitors and uses thereof
JP2010513318A (ja) ヘテロ環状化合物およびその使用方法
JP2022521797A (ja) イミプリドン様薬剤に対する薬物反応のバイオマーカとしてのカゼイン分解プロテアーゼpの機能の使用
EP2408450B1 (en) Alpha-(n-sulfonamido)acetamide compound as an inhibitor of beta amyloid peptide production
JP2007514414A (ja) c−Rel依存性サイトカイン産生を調節する組成物及び方法
TW201038266A (en) Novel alpha-(N-sulfonamido)acetamide compounds incorporating deuterium as inhibitors of beta amyloid peptide production
ES2322641T3 (es) Compuestos cataliticos.
US8093276B2 (en) Alpha-(N-sulfonamido)acetamide compound as an inhibitor of beta amyloid peptide production
HK1141801B (en) A novel alpha-(n-sulfonamido)acetamide compound as an inhibitor of beta amyloid peptide production
WO2026018015A2 (en) Novel methods and uses
HK40076614A (en) Inhibitors of hif-2alpha
MX2008007980A (en) Inhibitors of ccr9 activity

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C02 Deemed withdrawal of patent application after publication (patent law 2001)
WD01 Invention patent application deemed withdrawn after publication

Application publication date: 20121010