MA37830B1 - Composés hétéroromatiques en tant qu'inhibiteurs de la tyrosine kinase de bruton (btk) - Google Patents

Composés hétéroromatiques en tant qu'inhibiteurs de la tyrosine kinase de bruton (btk)

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Publication number
MA37830B1
MA37830B1 MA37830A MA37830A MA37830B1 MA 37830 B1 MA37830 B1 MA 37830B1 MA 37830 A MA37830 A MA 37830A MA 37830 A MA37830 A MA 37830A MA 37830 B1 MA37830 B1 MA 37830B1
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MA
Morocco
Prior art keywords
compounds
heteroromatic
btk
inhibitors
tyrosine kinase
Prior art date
Application number
MA37830A
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English (en)
Other versions
MA20150290A1 (fr
Inventor
Joerg Martin Bentzien
Angela Kay Berry
Todd Bosanac
Michael Burke
Darren Disalvo
Joshua Horan
Shuang Liang
Can Mao
Wang Mao
Yue Shen
Fariba Soleymanzadeh
Renee Zindell
Original Assignee
Boehringer Ingelheim Int
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Application filed by Boehringer Ingelheim Int filed Critical Boehringer Ingelheim Int
Publication of MA20150290A1 publication Critical patent/MA20150290A1/fr
Publication of MA37830B1 publication Critical patent/MA37830B1/fr

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    • 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
    • C07D417/02Heterocyclic 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 two hetero rings
    • C07D417/08Heterocyclic 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 two hetero rings linked by a carbon chain containing alicyclic rings
    • 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
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    • A61P17/00Drugs for dermatological disorders
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    • C07D231/14Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three 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, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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    • C07D231/14Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three 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, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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    • C07D231/10Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/14Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three 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, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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    • C07D277/20Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D277/32Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three 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, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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    • 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
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    • 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
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    • C07D417/04Heterocyclic 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 two hetero rings directly linked by a ring-member-to-ring-member bond
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    • C07D417/02Heterocyclic 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 two hetero rings
    • C07D417/06Heterocyclic 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 two hetero rings linked by a carbon chain containing only aliphatic carbon atoms

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
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  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Immunology (AREA)
  • Pulmonology (AREA)
  • Dermatology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Rheumatology (AREA)
  • Pain & Pain Management (AREA)
  • Ophthalmology & Optometry (AREA)
  • Oncology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Hematology (AREA)
  • Transplantation (AREA)
  • Otolaryngology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Thiazole And Isothizaole Compounds (AREA)

Abstract

La présente invention concerne des composé de formule (i) où les groupes a, cy, xi et y sont définis ici, qui sont appropriés pour le traitement d'une maladie choisie parmi la polyarthrite rhumatoïde, le lupus érythromateux disséminé, la sclérodermie, l'asthme, la rhinite allergique, l'eczéma allergique, le lymphome à cellules b, la sclérose en plaques, la polyarthrite rhumatoïde juvénile, l'arthrite idiopathique juvénile, la maladie intestinale inflammatoire, la maladie du greffon contre l'hôte, l'arthrite psoriasique, la spondylarthrite ankylosante et l'uvéite.
MA37830A 2012-08-10 2013-08-08 Composés hétéroromatiques en tant qu'inhibiteurs de la tyrosine kinase de bruton (btk) MA37830B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201261681684P 2012-08-10 2012-08-10
PCT/US2013/054096 WO2014025976A1 (fr) 2012-08-10 2013-08-08 Composés hétéroromatiques en tant qu'inhibiteurs de la tyrosine kinase de bruton (btk)

Publications (2)

Publication Number Publication Date
MA20150290A1 MA20150290A1 (fr) 2015-08-31
MA37830B1 true MA37830B1 (fr) 2018-09-28

Family

ID=49029216

Family Applications (1)

Application Number Title Priority Date Filing Date
MA37830A MA37830B1 (fr) 2012-08-10 2013-08-08 Composés hétéroromatiques en tant qu'inhibiteurs de la tyrosine kinase de bruton (btk)

Country Status (25)

Country Link
US (5) US20140045813A1 (fr)
EP (1) EP2882741B1 (fr)
JP (1) JP6348492B2 (fr)
KR (1) KR20150040292A (fr)
CN (1) CN104603124B (fr)
AP (1) AP2015008203A0 (fr)
AU (1) AU2013299557B2 (fr)
BR (1) BR112015002590A2 (fr)
CA (1) CA2881519A1 (fr)
CL (1) CL2015000256A1 (fr)
EA (1) EA029210B1 (fr)
EC (1) ECSP15008851A (fr)
GE (1) GEP201706748B (fr)
HK (1) HK1210161A1 (fr)
IL (1) IL236495A0 (fr)
IN (1) IN2015DN00524A (fr)
MA (1) MA37830B1 (fr)
MX (1) MX2015001802A (fr)
NZ (1) NZ703607A (fr)
PE (1) PE20150756A1 (fr)
PH (1) PH12015500294B1 (fr)
SA (1) SA515360007B1 (fr)
SG (1) SG11201500499TA (fr)
TN (1) TN2015000029A1 (fr)
WO (1) WO2014025976A1 (fr)

Families Citing this family (34)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2013299557B2 (en) 2012-08-10 2017-06-22 Boehringer Ingelheim International Gmbh Heteroaromatic compounds as Bruton's tyrosine kinase (BTK) inhibitors
AP2015008381A0 (en) * 2012-11-02 2015-04-30 Pfizer Bruton's tyrosine kinase inhibitors
CN103848810A (zh) * 2012-11-30 2014-06-11 北京赛林泰医药技术有限公司 鲁顿酪氨酸激酶抑制剂
JP6403751B2 (ja) 2013-03-14 2018-10-10 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング 5−チアゾールカルボキサミン誘導体及びbtk阻害剤としてのその使用
WO2014152114A1 (fr) 2013-03-15 2014-09-25 Boehringer Ingelheim International Gmbh Composés hétéroaromatiques en tant qu'inhibiteurs de btk
PE20151652A1 (es) * 2013-03-15 2015-11-12 Janssen Pharmaceutica Nv Proceso e intermedios para preparar un medicamento
SG11201602070TA (en) 2013-09-30 2016-04-28 Beijing Synercare Pharma Tech Co Ltd Substituted nicotinimide inhibitors of btk and their preparation and use in the treatment of cancer, inflammation and autoimmune disease
US9512084B2 (en) 2013-11-29 2016-12-06 Novartis Ag Amino pyrimidine derivatives
US9828364B2 (en) * 2014-01-29 2017-11-28 Boehringer Ingelheim International Gmbh Pyrazole compounds as BTK inhibitors
WO2015185998A2 (fr) * 2014-04-11 2015-12-10 Acerta Pharma B.V. Procédés de blocage de la voie de signalisation des cxcr-4/sdf-1 à l'aide d'inhibiteurs de kinase x de moelle osseuse
CN105085474B (zh) * 2014-05-07 2018-05-18 北京赛林泰医药技术有限公司 鲁顿酪氨酸激酶抑制剂
CN105884747B (zh) * 2014-08-28 2021-01-05 首药控股(北京)有限公司 一种制备布鲁顿酪氨酸激酶(btk)激酶抑制剂的制备方法
CN114591242A (zh) 2015-12-16 2022-06-07 洛克索肿瘤学股份有限公司 可用作激酶抑制剂的化合物
US9975882B2 (en) 2015-12-16 2018-05-22 Boehringer Ingelheim International Gmbh Heteroaromatic compounds as BTK inhibitors
CN105646318A (zh) * 2015-12-30 2016-06-08 武汉药明康德新药开发有限公司 一种2-叔丁氧羰基-5-氮杂螺环[3.3]庚烷-6-羧酸的合成方法
EP3402789B1 (fr) 2016-01-13 2020-03-18 Boehringer Ingelheim International Gmbh Isoquinolones comme inhibiteurs de btk
CN107226805A (zh) * 2016-03-24 2017-10-03 北京天诚医药科技有限公司 芳香族酰胺类衍生物、其制备方法及其在医药上的应用
CN109641965A (zh) 2016-08-15 2019-04-16 诺华股份有限公司 使用奥法木单抗治疗多发性硬化的方案和方法
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