SG10201809696UA - Processes and intermediates for preparing a medicament - Google Patents

Processes and intermediates for preparing a medicament

Info

Publication number
SG10201809696UA
SG10201809696UA SG10201809696UA SG10201809696UA SG10201809696UA SG 10201809696U A SG10201809696U A SG 10201809696UA SG 10201809696U A SG10201809696U A SG 10201809696UA SG 10201809696U A SG10201809696U A SG 10201809696UA SG 10201809696U A SG10201809696U A SG 10201809696UA
Authority
SG
Singapore
Prior art keywords
intermediates
processes
medicament
preparing
useful
Prior art date
Application number
SG10201809696UA
Inventor
Philip Pye
Haim Cyril Ben
Matteo Conza
Ioannis Nicolaos Houpis
Original Assignee
Janssen Pharmaceutica Nv
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 Janssen Pharmaceutica Nv filed Critical Janssen Pharmaceutica Nv
Publication of SG10201809696UA publication Critical patent/SG10201809696UA/en

Links

Classifications

    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond

Abstract

PROCESSES AND INTERMEDIATES FOR PREPARING A MEDICAMENT 5 Disclosed is a process for the preparation of the following compounds: NH2 N N O N R 1 NC NH2 N N R 2a N R 1 R 1a where R 1, R1a and R 2a have the definitions in the description, as well as a process to 10 prepare other intermediates that may be useful to synthesise downstream products, especially compounds that are useful as medicaments, for instance Bruton’s tyrosine kinase (Btk) inhibitors such as ibrutinib. Also disclosed are other processes, other intermediates and compounds per se . 15 [No available fig.]
SG10201809696UA 2013-03-15 2014-03-11 Processes and intermediates for preparing a medicament SG10201809696UA (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201361786842P 2013-03-15 2013-03-15
EP13159470 2013-03-15
EP13197813 2013-12-17

Publications (1)

Publication Number Publication Date
SG10201809696UA true SG10201809696UA (en) 2018-11-29

Family

ID=51535892

Family Applications (2)

Application Number Title Priority Date Filing Date
SG10201809696UA SG10201809696UA (en) 2013-03-15 2014-03-11 Processes and intermediates for preparing a medicament
SG11201507595XA SG11201507595XA (en) 2013-03-15 2014-03-11 Processes and intermediates for preparing a medicament

Family Applications After (1)

Application Number Title Priority Date Filing Date
SG11201507595XA SG11201507595XA (en) 2013-03-15 2014-03-11 Processes and intermediates for preparing a medicament

Country Status (19)

Country Link
EP (1) EP2970291B1 (en)
JP (1) JP6777398B2 (en)
KR (2) KR102311329B1 (en)
CN (2) CN105026400A (en)
AU (2) AU2014230935A1 (en)
BR (1) BR112015021856A2 (en)
CA (1) CA2901510C (en)
DK (1) DK2970291T3 (en)
EA (1) EA201591685A1 (en)
ES (1) ES2924193T3 (en)
HR (1) HRP20220628T1 (en)
HU (1) HUE058914T2 (en)
LT (1) LT2970291T (en)
MX (2) MX2015012731A (en)
MY (1) MY194905A (en)
PE (1) PE20151652A1 (en)
SG (2) SG10201809696UA (en)
SI (1) SI2970291T1 (en)
WO (1) WO2014139970A1 (en)

Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2846652C (en) 2011-09-02 2019-11-05 Incyte Corporation Heterocyclylamines as pi3k inhibitors
CN105884747B (en) * 2014-08-28 2021-01-05 首药控股(北京)有限公司 Preparation method for preparing Bruton's Tyrosine Kinase (BTK) kinase inhibitor
CN104447761A (en) * 2014-11-27 2015-03-25 广东东阳光药业有限公司 Method for preparing pyrazole derivative
EP3248979B1 (en) 2015-01-21 2021-04-14 Hefei Institutes of Physical Science, Chinese Academy of Sciences Novel inhibitor of flt3 kinase and use thereof
CN105481862B (en) * 2015-01-21 2018-08-21 中国科学院合肥物质科学研究院 The new inhibitor and application thereof of FLT3 kinases
MY187502A (en) * 2015-02-27 2021-09-24 Incyte Corp Salts of pi3k inhibitor and processes for their preparation
LV15201B (en) * 2015-08-31 2017-07-20 Latvijas Organiskās Sintēzes Institūts The method for the preparation of ibrutinib intermediate
CN106608877B (en) * 2015-10-21 2018-11-13 新发药业有限公司 One kind replacing Buddhist nun's intermediate 4- amino -3- according to Shandong(4- phenoxy groups)The preparation method of phenyl -1H- pyrazolos [3,4-d] pyrimidine
JO3793B1 (en) 2015-12-10 2021-01-31 Janssen Pharmaceutica Nv Inhibitors of bruton’s tyrosine kinase and methods of their use
JO3794B1 (en) 2015-12-10 2021-01-31 Janssen Pharmaceutica Nv Polycyclic compounds as inhibitors of bruton's tyrosine kinase
WO2018103058A1 (en) * 2016-12-09 2018-06-14 Janssen Pharmaceutica Nv Inhibitors of bruton's tyrosine kinase and methods of their use
WO2018145280A1 (en) * 2017-02-09 2018-08-16 合肥合源药业有限公司 Flt3 kinase inhibitor or crystal forms of salt thereof and preparation method therefor
CN107383017B (en) * 2017-07-20 2020-01-14 河南师范大学 Efficient preparation method of ibrutinib
US20200369611A1 (en) * 2017-08-01 2020-11-26 Boehringer Ingelheim International Gmbh Intermediate compounds and methods
CN113906011A (en) * 2019-05-21 2022-01-07 詹森药业有限公司 Processes and intermediates for preparing BTK inhibitors
CA3135240A1 (en) 2019-05-21 2020-11-26 Philip James Pye Processes and intermediates for preparing a btk inhibitor
CN113200987A (en) * 2021-04-29 2021-08-03 湖南华腾制药有限公司 Preparation method of ibrutinib
CN115322226B (en) * 2022-08-17 2023-08-11 厦门大学 Covalent targeting arsenic inhibitor and preparation method and application thereof

Family Cites Families (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SK3812002A3 (en) * 1999-09-17 2003-09-11 Abbott Gmbh & Co Kg Pyrazolopyrimidines as therapeutic agents
WO2008121742A2 (en) * 2007-03-28 2008-10-09 Pharmacyclics, Inc. Inhibitors of bruton's tyrosine kinase
ES2585902T3 (en) * 2006-09-22 2016-10-10 Pharmacyclics Llc Bruton tyrosine kinase inhibitors
WO2008054827A2 (en) * 2006-11-03 2008-05-08 Pharmacyclics, Inc. Bruton's tyrosine kinase activity probe and method of using
UA105362C2 (en) * 2008-04-02 2014-05-12 Бьорингер Ингельхайм Интернациональ Гмбх 1-heterocyclyl-1, 5-dihydro-pyrazolo [3, 4-d] pyrimidin-4-one derivatives and their use as pde9a modulators
ES2460019T3 (en) 2009-03-31 2014-05-13 Boehringer Ingelheim International Gmbh Derivatives of 1-heterocyclyl-1,5-dihydro-pyrazolo [3,4-d] pyrimidin-4-one and its use as PDE9A modulators
US7718662B1 (en) * 2009-10-12 2010-05-18 Pharmacyclics, Inc. Pyrazolo-pyrimidine inhibitors of bruton's tyrosine kinase
CA2804648C (en) * 2010-07-09 2019-01-22 The Walter And Eliza Hall Institute Of Medical Research Protein kinase inhibitors and methods of treatment
EP2632898A4 (en) * 2010-10-29 2014-04-02 Biogen Idec Inc Heterocyclic tyrosine kinase inhibitors
WO2012158795A1 (en) * 2011-05-17 2012-11-22 Principia Biopharma Inc. Pyrazolopyrimidine derivatives as tyrosine kinase inhibitors
EA201490265A1 (en) * 2011-07-13 2014-12-30 Фармасайкликс, Инк. BLUTON TYROSINKINASE INHIBITORS
CN104603124B (en) * 2012-08-10 2018-04-17 勃林格殷格翰国际有限公司 Heteroaromatics as bruton's tyrosine kinase (BTK) inhibitor
KR101668574B1 (en) * 2012-11-02 2016-10-24 화이자 인코포레이티드 Bruton's tyrosine kinase inhibitors
CN103848810A (en) * 2012-11-30 2014-06-11 北京赛林泰医药技术有限公司 Bruton's tyrosine kinases inhibitor

Also Published As

Publication number Publication date
SG11201507595XA (en) 2015-10-29
AU2018204086A1 (en) 2018-06-28
SI2970291T1 (en) 2022-07-29
AU2014230935A1 (en) 2015-09-03
EP2970291A1 (en) 2016-01-20
HUE058914T2 (en) 2022-09-28
BR112015021856A2 (en) 2017-07-18
KR20150132172A (en) 2015-11-25
EP2970291B1 (en) 2022-05-11
KR102377688B1 (en) 2022-03-22
MY194905A (en) 2022-12-22
KR20210123429A (en) 2021-10-13
HRP20220628T1 (en) 2022-06-24
JP2016510779A (en) 2016-04-11
EA201591685A1 (en) 2016-01-29
KR102311329B1 (en) 2021-10-14
CA2901510A1 (en) 2014-09-18
JP6777398B2 (en) 2020-10-28
PE20151652A1 (en) 2015-11-12
AU2018204086B2 (en) 2020-03-12
LT2970291T (en) 2022-06-10
DK2970291T3 (en) 2022-08-01
ES2924193T3 (en) 2022-10-05
MX2020012596A (en) 2021-02-09
CN105026400A (en) 2015-11-04
MX2015012731A (en) 2016-02-18
WO2014139970A1 (en) 2014-09-18
CA2901510C (en) 2022-11-29
CN112608298A (en) 2021-04-06

Similar Documents

Publication Publication Date Title
SG10201809696UA (en) Processes and intermediates for preparing a medicament
SA515360007B1 (en) Heteroaromatic compounds as bruton's tyrosine kinase (BTK) inhibitors
MX2021007432A (en) Compounds and compositions for inhibiting the activity of shp2.
TN2014000427A1 (en) Benzamide derivatives for inhibiting the activity of abl1, abl2 and bcr-abl1
PH12016500531A1 (en) Compound inhibiting activities of btk and/or jak3 kinases
MX357305B (en) Compounds and compositions for inhibiting the activity of abl1, abl2 and bcr-abl1.
TN2014000138A1 (en) Substituted benzylindazoles for use as bub1 kinase inhibitors in the treatment of hyperproliferative diseases.
EA030383B9 (en) Bicyclically substituted uracils, processes for preparation thereof, use thereof, medicament and method for treatment using same
MD20150048A2 (en) Pyrrolotriazinone derivatives as PI3K inhibitors
MX2016000794A (en) High potency pancreatin pharmaceutical compositions.
PH12016500003A1 (en) Compounds and compositions as inhibitors of mek
MY175804A (en) Estra-1,3,5(10),16-tetraene-3-carboxamide derivatives, process for preparation thereof, pharmaceutical preparations comprising them, and use thereof for production of medicaments
BR112015000443A2 (en) 3-substituted estra-1,3,5 (10), 16-tetraene derivatives, process for their manufacture, pharmaceutical preparations containing them, as well as their use for the production of medicaments
MX2016000480A (en) High potency pancreatin pharmaceutical compositions.
WO2017168454A3 (en) Novel compounds as btk inhibitors
PH12015502000A1 (en) Processes and intermediates for preparing a medicament
TH172968A (en) Process and substance for drug preparation
WO2014153113A3 (en) Processes and intermediates for the preparation of 3 amino-n-cyclopropyl-2 hydroxypropionamide derivatives
TN2014000085A1 (en) Substituted annellated pyrimidine and the use thereof