CA3112072C - Biocatalytical process for the preparation of isoxazolyl-methoxy-nicotinic acids - Google Patents

Biocatalytical process for the preparation of isoxazolyl-methoxy-nicotinic acids Download PDF

Info

Publication number
CA3112072C
CA3112072C CA3112072A CA3112072A CA3112072C CA 3112072 C CA3112072 C CA 3112072C CA 3112072 A CA3112072 A CA 3112072A CA 3112072 A CA3112072 A CA 3112072A CA 3112072 C CA3112072 C CA 3112072C
Authority
CA
Canada
Prior art keywords
compound
formula
isoxazol
methyl
ylmethoxy
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.)
Active
Application number
CA3112072A
Other languages
English (en)
French (fr)
Other versions
CA3112072A1 (en
Inventor
Pascal Dott
Steven Paul Hanlon
Stefan Hildbrand
Hans Iding
Andrew Thomas
Pius Waldmeier
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.)
F Hoffmann La Roche AG
Original Assignee
F Hoffmann La Roche AG
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 F Hoffmann La Roche AG filed Critical F Hoffmann La Roche AG
Publication of CA3112072A1 publication Critical patent/CA3112072A1/en
Application granted granted Critical
Publication of CA3112072C publication Critical patent/CA3112072C/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12PFERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P17/00Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms
    • C12P17/16Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms containing two or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12YENZYMES
    • C12Y305/00Hydrolases acting on carbon-nitrogen bonds, other than peptide bonds (3.5)
    • C12Y305/05Hydrolases acting on carbon-nitrogen bonds, other than peptide bonds (3.5) in nitriles (3.5.5)
    • C12Y305/05001Nitrilase (3.5.5.1)

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Zoology (AREA)
  • Genetics & Genomics (AREA)
  • General Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Microbiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Biotechnology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
CA3112072A 2011-10-20 2012-10-17 Biocatalytical process for the preparation of isoxazolyl-methoxy-nicotinic acids Active CA3112072C (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP11185992.2 2011-10-20
EP11185992 2011-10-20
CA2850440A CA2850440C (en) 2011-10-20 2012-10-17 Process for the preparation of isoxazolyl-methoxy-nicotinic acids

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
CA2850440A Division CA2850440C (en) 2011-10-20 2012-10-17 Process for the preparation of isoxazolyl-methoxy-nicotinic acids

Publications (2)

Publication Number Publication Date
CA3112072A1 CA3112072A1 (en) 2013-04-25
CA3112072C true CA3112072C (en) 2023-06-13

Family

ID=47019026

Family Applications (2)

Application Number Title Priority Date Filing Date
CA3112072A Active CA3112072C (en) 2011-10-20 2012-10-17 Biocatalytical process for the preparation of isoxazolyl-methoxy-nicotinic acids
CA2850440A Active CA2850440C (en) 2011-10-20 2012-10-17 Process for the preparation of isoxazolyl-methoxy-nicotinic acids

Family Applications After (1)

Application Number Title Priority Date Filing Date
CA2850440A Active CA2850440C (en) 2011-10-20 2012-10-17 Process for the preparation of isoxazolyl-methoxy-nicotinic acids

Country Status (20)

Country Link
US (1) US8604062B2 (https=)
EP (1) EP2768827B1 (https=)
JP (1) JP5923174B2 (https=)
KR (2) KR20140084209A (https=)
CN (1) CN103889978B (https=)
AR (1) AR088358A1 (https=)
AU (1) AU2012321095B2 (https=)
BR (1) BR112014009266B1 (https=)
CA (2) CA3112072C (https=)
DK (1) DK2768827T3 (https=)
ES (1) ES2613802T3 (https=)
HU (1) HUE031276T2 (https=)
IL (1) IL231645A (https=)
MX (1) MX2014004688A (https=)
MY (1) MY164880A (https=)
PL (1) PL2768827T3 (https=)
RU (1) RU2014118966A (https=)
SG (1) SG11201401626UA (https=)
SI (1) SI2768827T1 (https=)
WO (1) WO2013057123A1 (https=)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BR112020004116A2 (pt) * 2017-08-28 2020-09-01 University Of Maryland, Baltimore novos moduladores do receptor de ácido gama aminobutírico tipo a para distúrbios de humor
IL279266B2 (en) 2018-06-13 2024-03-01 Hoffmann La Roche New isoxazolyl ether derivatives as gaba a alpha5 pam
HU231223B1 (hu) 2018-09-28 2022-01-28 Richter Gedeon Nyrt. GABAA A5 receptor modulátor hatású biciklusos vegyületek
EP4126858B1 (en) 2020-03-26 2026-03-18 Richter Gedeon Nyrt. Dihydro-2-pyrrolo[3,4-c]pyridine derivatives as gabaa a5 receptor modulators
GB202013765D0 (en) * 2020-09-02 2020-10-14 Gw Res Ltd Method of preparing cannabinoids
CN116854680A (zh) 2022-03-28 2023-10-10 上海赛默罗生物科技有限公司 异噁唑-杂环类衍生物、药物组合物和用途
CN119265168B (zh) * 2024-11-05 2025-06-20 江南大学 一种新型腈水解酶及其在烟酸生物合成中的应用

Family Cites Families (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1102755B1 (en) 1998-08-07 2006-01-04 Chiron Corporation Substituted isoxazole derivatives as estrogen receptor modulators
US6551804B2 (en) * 1999-07-12 2003-04-22 E. I. Du Pont De Nemours And Company Process for preparing 4-cyanopentanoic acid
US20060148858A1 (en) 2002-05-24 2006-07-06 Tsuyoshi Maekawa 1, 2-Azole derivatives with hypoglycemic and hypolipidemic activity
GB0221443D0 (en) 2002-09-16 2002-10-23 Glaxo Group Ltd Pyridine derivates
UA82292C2 (uk) * 2004-04-14 2008-03-25 Пфайзер Продактс Инк. Спосіб стереоселективного біоперетворення аліфатичних динітрилів в ціанокарбонові кислоти (варіанти)
WO2005113519A1 (en) 2004-05-14 2005-12-01 Irm Llc Compounds and compositions as ppar modulators
ATE415385T1 (de) 2004-10-01 2008-12-15 Hoffmann La Roche Hexafluorisopropanolsubstituierte etherderivate
DE602006017694D1 (de) 2005-06-27 2010-12-02 Bristol Myers Squibb Co C-verknüpfte zyklische antagonisten des p2y1-rezeptors mit eignung bei der behandlung thrombotischer leiden
EP1931661B1 (en) 2005-09-19 2008-11-19 F.Hoffmann-La Roche Ag Isoxazolo derivatives as gaba a alpha5 inverse agonists
WO2007042420A1 (en) 2005-10-11 2007-04-19 F. Hoffmann-La Roche Ag Isoxazole derivatives
RU2426731C2 (ru) 2005-12-23 2011-08-20 Ф. Хоффманн-Ля Рош Аг Производные арил-изоксазоло-4-ил-оксадиазола
WO2009071464A1 (en) 2007-12-04 2009-06-11 F. Hoffmann-La Roche Ag Isoxazolo-pyrazine derivatives
US7943619B2 (en) 2007-12-04 2011-05-17 Hoffmann-La Roche Inc. Isoxazolo-pyridazine derivatives
UA100132C2 (en) * 2007-12-04 2012-11-26 Ф. Хоффманн-Ля Рош Аг Isoxazolo-pyridine derivatives
JP2012040448A (ja) * 2008-11-14 2012-03-01 Yasutaka Sakamoto マイクロバブル発生装置
US8222246B2 (en) 2009-04-02 2012-07-17 Hoffmann-La Roche Inc. Substituted isoxazoles
MX2011011484A (es) 2009-05-07 2011-11-18 Hoffmann La Roche Derivados de isoxazol-piridina como moduladores del acido gamma-aminobutirico.

Also Published As

Publication number Publication date
WO2013057123A1 (en) 2013-04-25
PL2768827T3 (pl) 2017-05-31
KR20200008671A (ko) 2020-01-28
CA2850440C (en) 2021-05-04
EP2768827A1 (en) 2014-08-27
KR20140084209A (ko) 2014-07-04
JP5923174B2 (ja) 2016-05-24
IL231645A (en) 2016-09-29
BR112014009266A2 (pt) 2017-06-13
BR112014009266B1 (pt) 2021-05-04
DK2768827T3 (en) 2017-02-13
JP2014530831A (ja) 2014-11-20
US20130102778A1 (en) 2013-04-25
AU2012321095B2 (en) 2015-08-20
BR112014009266A8 (pt) 2020-04-22
KR102262697B1 (ko) 2021-06-11
RU2014118966A (ru) 2015-11-27
NZ622214A (en) 2016-08-26
CA3112072A1 (en) 2013-04-25
HUE031276T2 (hu) 2017-07-28
MY164880A (en) 2018-01-30
ES2613802T3 (es) 2017-05-26
CN103889978B (zh) 2017-02-15
CN103889978A (zh) 2014-06-25
CA2850440A1 (en) 2013-04-25
SG11201401626UA (en) 2014-05-29
AU2012321095A1 (en) 2013-05-09
IL231645A0 (en) 2014-05-28
US8604062B2 (en) 2013-12-10
EP2768827B1 (en) 2016-11-23
AR088358A1 (es) 2014-05-28
SI2768827T1 (sl) 2017-04-26
MX2014004688A (es) 2014-05-28

Similar Documents

Publication Publication Date Title
CA3112072C (en) Biocatalytical process for the preparation of isoxazolyl-methoxy-nicotinic acids
AU2019257457B2 (en) Bicyclic compounds as autotaxin (ATX) and lysophosphatidic acid (LPA) production inhibitors
US9926313B2 (en) Imidazopyridine derivatives as modulators of TNF activity
US9273053B2 (en) Sulfur-containing heterocyclic derivative having Beta secretase inhibitory activity
JP6483701B2 (ja) Tnf活性のモジュレーターとしてのベンゾトリアゾール誘導体
ES2809535T3 (es) Derivados de imidazopiridina como moduladores de la actividad de TNF
ES2817052T3 (es) Derivados de imidazopiridazina como moduladores de la actividad de TNF
JP6483702B2 (ja) Tnf活性のモジュレーターとしてのテトラヒドロベンゾイミダゾール誘導体
KR101584925B1 (ko) Pde10a 억제제로서의 트라이아졸로피리딘 화합물
JP6426185B2 (ja) Tnf活性のモジュレーターとしてのトリアゾロピリジン誘導体
US20110224231A1 (en) Novel Lactams as Beta Secretase Inhibitors
EA026062B1 (ru) Производные пиразолкарбоксамида в качестве модуляторов рецепторов следовых аминов (taar) для применения при лечении различных расстройств, таких как депрессия, диабет и болезнь паркинсона
SG11202111162PA (en) Pyridin-3-yl derivatives
NZ622214B2 (en) Process for the preparation of isoxazolyl-methoxy-nicotinic acids
US20120283239A1 (en) 1H-[1,2,3]TRIAZOLO[4,5-c]PYRIDINE-4-CARBONITRILE DERIVATIVES
HK1193610A (en) Process for the preparation of isoxazolyl-methoxy-nicotinic acids
HK1193610B (en) Process for the preparation of isoxazolyl-methoxy-nicotinic acids

Legal Events

Date Code Title Description
EEER Examination request

Effective date: 20210312

MPN Maintenance fee for patent paid

Free format text: FEE DESCRIPTION TEXT: MF (PATENT, 12TH ANNIV.) - STANDARD

Year of fee payment: 12

U00 Fee paid

Free format text: ST27 STATUS EVENT CODE: A-4-4-U10-U00-U101 (AS PROVIDED BY THE NATIONAL OFFICE); EVENT TEXT: MAINTENANCE REQUEST RECEIVED

Effective date: 20240923

U11 Full renewal or maintenance fee paid

Free format text: ST27 STATUS EVENT CODE: A-4-4-U10-U11-U102 (AS PROVIDED BY THE NATIONAL OFFICE); EVENT TEXT: MAINTENANCE FEE PAYMENT DETERMINED COMPLIANT

Effective date: 20240923

Free format text: ST27 STATUS EVENT CODE: A-4-4-U10-U11-U102 (AS PROVIDED BY THE NATIONAL OFFICE); EVENT TEXT: MAINTENANCE FEE PAYMENT PAID IN FULL

Effective date: 20240923

MPN Maintenance fee for patent paid

Free format text: FEE DESCRIPTION TEXT: MF (PATENT, 13TH ANNIV.) - STANDARD

Year of fee payment: 13

U00 Fee paid

Free format text: ST27 STATUS EVENT CODE: A-4-4-U10-U00-U101 (AS PROVIDED BY THE NATIONAL OFFICE); EVENT TEXT: MAINTENANCE REQUEST RECEIVED

Effective date: 20251010

U11 Full renewal or maintenance fee paid

Free format text: ST27 STATUS EVENT CODE: A-4-4-U10-U11-U102 (AS PROVIDED BY THE NATIONAL OFFICE); EVENT TEXT: MAINTENANCE FEE PAYMENT PAID IN FULL

Effective date: 20251010