SG11201901251SA - Aminopyrimidines as alk inhibitors - Google Patents

Aminopyrimidines as alk inhibitors

Info

Publication number
SG11201901251SA
SG11201901251SA SG11201901251SA SG11201901251SA SG11201901251SA SG 11201901251S A SG11201901251S A SG 11201901251SA SG 11201901251S A SG11201901251S A SG 11201901251SA SG 11201901251S A SG11201901251S A SG 11201901251SA SG 11201901251S A SG11201901251S A SG 11201901251SA
Authority
SG
Singapore
Prior art keywords
international
pct
co7d
english
august
Prior art date
Application number
SG11201901251SA
Inventor
Shaomeng Wang
Jianyong Chen
Original Assignee
Univ Michigan Regents
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 Univ Michigan Regents filed Critical Univ Michigan Regents
Publication of SG11201901251SA publication Critical patent/SG11201901251SA/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero 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
    • A61K31/495Heterocyclic 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
    • A61K31/506Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • 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
    • C07D401/12Heterocyclic 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 linked by a chain containing hetero atoms as chain links

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Epidemiology (AREA)
  • Pain & Pain Management (AREA)
  • Engineering & Computer Science (AREA)
  • Immunology (AREA)
  • Rheumatology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

NO H Kr NH 0-R6 R 7 R2a Rib N R2b R3 (12) INTERNATIONAL APPLICATION PUBLISHED UNDER THE PATENT COOPERATION TREATY (PCT) (19) World Intellectual Property Organization International Bureau (43) International Publication Date 08 March 2018 (08.03.2018) WIP0 I PCT o mono °nolo olo Ho Ho Imo (10) International Publication Number WO 2018/044767 A2 (51) International Patent Classification: CO7D 405/14 (2006.01) A61P 35/00 CO7D 401/12 (2006.01) A61P 29/00 A61K 31/506 (2006.01) A61P 37/00 (21) International Application Number: PCT/US2017/048845 (22) International Filing Date: 28 August 2017 (28.08.2017) (25) Filing Language: English (26) Publication Language: English (30) Priority Data: 62/380,818 29 August 2016 (29.08.2016) US (71) Applicant: THE REGENTS OF THE UNIVERSITY OF MICHIGAN [US/US]; Office Of Technology Trans- fer, 1600 Huron Parkway, 2nd Floor, Ann Arbor, MI 48109-2590 (US). (72) Inventors: WANG, Shaomeng; 3336 Stirling Ct., Superi- or Township, MI 49198 (US). CHEN, Jianyong; 2659 Ar- rowwood Trial, Ann Arbor, MI 48105 (US). (74) Agent: NAPOLI, James, J.; Marshall, Gerstein & Borun LLP, 233 S. Wacker Drive, 6300 Willis Tower, Chicago, IL 60606-6357 (US). (81) Designated States (unless otherwise indicated, for every kind of national protection available): AE, AG, AL, AM, AO, AT, AU, AZ, BA, BB, BG, BH, BN, BR, BW, BY, BZ, CA, CH, CL, CN, CO, CR, CU, CZ, DE, DJ, DK, DM, DO, DZ, EC, EE, EG, ES, FI, GB, GD, GE, GH, GM, GT, HN, HR, HU, ID, IL, IN, IR, IS, JO, JP, KE, KG, KH, KN, KP, KR, KW, KZ, LA, LC, LK, LR, LS, LU, LY, MA, MD, ME, MG, MK, MN, MW, MX, MY, MZ, NA, NG, NI, NO, NZ, OM, PA, PE, PG, PH, PL, PT, QA, RO, RS, RU, RW, SA, SC, SD, SE, SG, SK, SL, SM, ST, SV, SY, TH, TJ, TM, TN, TR, TT, TZ, UA, UG, US, UZ, VC, VN, ZA, ZM, ZW. (84) Designated States (unless otherwise indicated, for every kind of regional protection available): ARIPO (BW, GH, GM, KE, LR, LS, MW, MZ, NA, RW, SD, SL, ST, SZ, TZ, UG, ZM, ZW), Eurasian (AM, AZ, BY, KG, KZ, RU, TJ, TM), European (AL, AT, BE, BG, CH, CY, CZ, DE, DK, EE, ES, FI, FR, GB, GR, HR, HU, IE, IS, IT, LT, LU, LV, MC, MK, MT, NL, NO, PL, PT, RO, RS, SE, SI, SK, SM, TR), OAPI (BF, BJ, CF, CG, CI, CM, GA, GN, GQ, GW, KM, ML, MR, NE, SN, TD, TG). Published: without international search report and to be republished upon receipt of that report (Rule 48.2(g)) (2006.01) (2006.01) (2006.01) W O 20 18/0 447 67 A2 (54) Title: AMINOPYRIMIDINES AS ALK INHIBITORS (57) : The present disclosure provides compounds represented by For- mula (I): and the pharmaceutically acceptable salts, hydrates, and solvates there- 5 of, wherein R ia , R ib , R , R , R, R, R 2a 2b 3 4 5 , R 6 , and R 7 are as defined as set forth in the specification. The present disclosure also provides compounds of Formu- la (I) for use to treat a condition or disorder responsive to inhibition of ALK such as cancer.
SG11201901251SA 2016-08-29 2017-08-28 Aminopyrimidines as alk inhibitors SG11201901251SA (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201662380818P 2016-08-29 2016-08-29
PCT/US2017/048845 WO2018044767A2 (en) 2016-08-29 2017-08-28 Aminopyrimidines as alk inhibitors

Publications (1)

Publication Number Publication Date
SG11201901251SA true SG11201901251SA (en) 2019-03-28

Family

ID=59846649

Family Applications (2)

Application Number Title Priority Date Filing Date
SG11201901251SA SG11201901251SA (en) 2016-08-29 2017-08-28 Aminopyrimidines as alk inhibitors
SG10201914030UA SG10201914030UA (en) 2016-08-29 2017-08-28 Aminopyrimidines as alk inhibitors

Family Applications After (1)

Application Number Title Priority Date Filing Date
SG10201914030UA SG10201914030UA (en) 2016-08-29 2017-08-28 Aminopyrimidines as alk inhibitors

Country Status (13)

Country Link
US (2) US10709705B2 (en)
EP (2) EP3504203B1 (en)
JP (2) JP7094566B2 (en)
KR (1) KR102530871B1 (en)
CN (2) CN109715620B (en)
AU (2) AU2017319135B2 (en)
BR (1) BR112019003897A2 (en)
CA (1) CA3033223A1 (en)
IL (1) IL264638B (en)
MX (2) MX2019002393A (en)
NZ (1) NZ751713A (en)
SG (2) SG11201901251SA (en)
WO (1) WO2018044767A2 (en)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11478477B2 (en) 2018-07-31 2022-10-25 Ascentage Pharma (Suzhou) Co., Ltd. Method for treating cancer by combination of FAK/ALK/ROS1 inhibitor and EGFR inhibitor
CN111171033B (en) * 2018-11-09 2021-11-02 天津大学 Pyrimidine derivative and synthesis method and application thereof
MX2021009863A (en) 2019-03-21 2021-11-12 Onxeo A dbait molecule in combination with kinase inhibitor for the treatment of cancer.
CN110143947B (en) * 2019-05-29 2021-10-15 华东师范大学 Preparation method of ceritinib analogue
US20220117964A1 (en) * 2019-06-25 2022-04-21 Ascentage Pharma (Suzhu) Co., Ltd. Combination of fak inhibitor and btk inhibitor for treating a disease
EP4054579A1 (en) 2019-11-08 2022-09-14 Institut National de la Santé et de la Recherche Médicale (INSERM) Methods for the treatment of cancers that have acquired resistance to kinase inhibitors
WO2021148581A1 (en) 2020-01-22 2021-07-29 Onxeo Novel dbait molecule and its use
US20230381176A1 (en) * 2020-09-25 2023-11-30 Ascentage Pharma (Suzhou) Co., Ltd. A pharmaceutical composition and use thereof for treatment of cancer
WO2022222932A1 (en) * 2021-04-19 2022-10-27 Ascentage Pharma (Suzhou) Co., Ltd. A pharmaceutical combination and use thereof

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5093330A (en) 1987-06-15 1992-03-03 Ciba-Geigy Corporation Staurosporine derivatives substituted at methylamino nitrogen
GB0004888D0 (en) 2000-03-01 2000-04-19 Astrazeneca Uk Ltd Chemical compounds
GB0305929D0 (en) 2003-03-14 2003-04-23 Novartis Ag Organic compounds
ES2424881T3 (en) 2003-08-15 2013-10-09 Novartis Ag 2,4-Di (phenylamino) -pyrimidines useful in the treatment of neoplastic diseases, inflammatory and immune system disorders
CN100584832C (en) * 2003-09-18 2010-01-27 诺瓦提斯公司 2,4-di (phenylamino) pyrimidines useful in the treatment of proliferative disorders
RS52545B (en) * 2004-04-07 2013-04-30 Novartis Ag Inhibitors of iap
ES2524009T3 (en) 2006-12-08 2014-12-03 Irm Llc Compounds and compositions as protein kinase inhibitors
US8592432B2 (en) 2008-04-07 2013-11-26 Bei Chen Compounds and compositions as protein kinase inhibitors
US9273077B2 (en) 2008-05-21 2016-03-01 Ariad Pharmaceuticals, Inc. Phosphorus derivatives as kinase inhibitors
EP2627179A4 (en) 2010-10-14 2014-04-02 Ariad Pharma Inc Methods for inhibiting cell proliferation in egfr-driven cancers
EP2670401B1 (en) * 2011-02-02 2015-06-10 Novartis AG Methods of using alk inhibitors
CN104672214B (en) * 2013-12-03 2019-04-12 上海翰森生物医药科技有限公司 Compound and its preparation and purposes with ALK inhibitory activity
KR101656382B1 (en) * 2014-02-28 2016-09-09 한국화학연구원 pyrimidine-2,4-diamine derivatives and pharmaceutical composition for anti cancer containing the same as an active ingredient

Also Published As

Publication number Publication date
KR20190039760A (en) 2019-04-15
MX2022000376A (en) 2022-02-10
WO2018044767A3 (en) 2018-04-12
CA3033223A1 (en) 2018-03-08
IL264638B (en) 2021-08-31
AU2021203098A1 (en) 2021-06-10
NZ751713A (en) 2022-07-01
AU2021203098B2 (en) 2023-05-25
JP7094566B2 (en) 2022-07-04
WO2018044767A2 (en) 2018-03-08
US20190175595A1 (en) 2019-06-13
AU2017319135B2 (en) 2021-03-18
EP3504203B1 (en) 2022-09-28
MX2019002393A (en) 2019-07-08
EP3504203A2 (en) 2019-07-03
US20200330464A1 (en) 2020-10-22
SG10201914030UA (en) 2020-03-30
CN115043821A (en) 2022-09-13
US11110090B2 (en) 2021-09-07
KR102530871B1 (en) 2023-05-09
CN109715620A (en) 2019-05-03
CN109715620B (en) 2022-05-06
JP2022120151A (en) 2022-08-17
BR112019003897A2 (en) 2019-05-21
JP2019528307A (en) 2019-10-10
US10709705B2 (en) 2020-07-14
EP4001273A2 (en) 2022-05-25
AU2017319135A1 (en) 2019-04-04
EP4001273A3 (en) 2022-08-24

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