SG11201901954XA - 8-(azetidin-1-yl)-[1,2,4]triazolo[1,5-a]pyridinyl compounds, compositions and methods of use thereof - Google Patents

8-(azetidin-1-yl)-[1,2,4]triazolo[1,5-a]pyridinyl compounds, compositions and methods of use thereof

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Publication number
SG11201901954XA
SG11201901954XA SG11201901954XA SG11201901954XA SG11201901954XA SG 11201901954X A SG11201901954X A SG 11201901954XA SG 11201901954X A SG11201901954X A SG 11201901954XA SG 11201901954X A SG11201901954X A SG 11201901954XA SG 11201901954X A SG11201901954X A SG 11201901954XA
Authority
SG
Singapore
Prior art keywords
international
pct
applicant
rule
bda
Prior art date
Application number
SG11201901954XA
Inventor
Simon Charles Goodacre
Mark Zak
F Anthony Romero
Yun-Xing Cheng
Limin Cheng
Rongbao Hua
Original Assignee
Hoffmann La Roche
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 Hoffmann La Roche filed Critical Hoffmann La Roche
Publication of SG11201901954XA publication Critical patent/SG11201901954XA/en

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-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
    • A61K31/4353Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/06Antiasthmatics
    • 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]
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D519/00Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00

Abstract

INTERNATIONAL APPLICATION PUBLISHED UNDER THE PATENT COOPERATION TREATY (PCT) (19) World Intellectual Property 111111411 01E101011M 3E1 0 011101 IMI 100 11101101110 11110 1111 OEN Organization International Bureau (10) International Publication Number (43) International Publication Date ......0\" WO 2018/046409 Al 15 March 2018 (15.03.2018) WIP0 I PCT (51) International Patent Classification: OM, PA, PE, PG, PH, PL, PT, QA, RO, RS, RU, RW, SA, CO7D 471/04 (2006.01) A61P 29/00 (2006.01) SC, SD, SE, SG, SK, SL, SM, ST, SV, SY, TH, TJ, TM, TN, A61K 31/437 (2006.01) TR, TT, TZ, UA, UG, US, UZ, VC, VN, ZA, ZM, ZW. (21) International Application Number: (84) Designated States (unless otherwise indicated, for every PCT/EP2017/072034 kind of regional protection available): ARIPO (BW, GH, (22) International Filing Date: GM, KE, LR, LS, MW, MZ, NA, RW, SD, SL, ST, SZ, TZ, 02 September 2017 (02.09.2017) UG, ZM, ZW), Eurasian (AM, AZ, BY, KG, KZ, RU, TJ, TM), European (AL, AT, BE, BG, CH, CY, CZ, DE, DK, (25) Filing Language: English EE, ES, FI, FR, GB, GR, HR, HU, IE, IS, IT, LT, LU, LV, (26) Publication Language: English 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, (30) Priority Data: KM, ML, MR, NE, SN, TD, TG). PCT/CN2016/098215 06 September 2016 (06.09.2016) CN Declarations under Rule 4.17: — as to applicant's entitlement to apply for and be granted a (71) Applicant (for all designated States except US): F. HOFF- patent (Rule 4.17(ii)) MANN-LA ROCHE AG [CH/CH]; Grenzacherstrasse — as to the applicant's entitlement to claim the priority of the 124, 4070 Basel (CH). earlier application (Rule 4.17(iii)) (71) Applicant (for US only): GENENTECH, INC. [US/US]; — of inventorship (Rule 4.17(iv)) — 1 DNA Way, South San Francisco, California 94080 (US). Published: (72) Inventors: GOODACRE, Simon Charles; 8/9 Spire — with international search report (Art. 21(3)) = Green Centre, Flex Meadow, Harlow Essex CM195TR = (GB). ZAK, Mark; c/o Genentech, Inc., 1 DNA Way, South _ San Francisco, California 94080 (US). ROMERO, F. An- thony; Genentech, Inc., 1 DNA Way, South San Fran- = c/o cisco, California 94080 (US). CHENG, Yun-Xing; 6 Tai- _ he Road, BDA, Beijing 100176 (CN). CHENG, Limin; 6 = Tai-he Road, BDA, Beijing 100176 (CN). HUA, Rongbao; = = 6 Tai-he Road, BDA, Beijing 100176 (CN). (74) Agent: SCHIRLIN, Julien; Grenzacherstrasse 124, 4070 = Basel (CH). (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, = (54) Title: 8-(AZETIDIN-1-YL)41,2,4]TRIAZOLO[1,5-A]PYRIDINYL COMPOUNDS, COMPOSITIONS AND METHODS OF USE THEREOF Il R5 R5 4 C:r N 'N ''' R4 H N \" \"L-....-. 0 © 0 N N 1 1' N 3 RA N 0 N ---- 3 R 1 \" N 1 1' n R ic © ---.... N NC C Rz Il R 6 (1) R 6 (II) 0 N C (57) : Compounds of Formuula (I) and (II), or a stereoisomer, tautomer, solvate, prodrug or salt thereof, and methods of use as Janus kinase inhibitors are described herein.
SG11201901954XA 2016-09-06 2017-09-02 8-(azetidin-1-yl)-[1,2,4]triazolo[1,5-a]pyridinyl compounds, compositions and methods of use thereof SG11201901954XA (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CN2016098215 2016-09-06
PCT/EP2017/072034 WO2018046409A1 (en) 2016-09-06 2017-09-02 8-(azetidin-1-yl)-[1,2,4]triazolo[1,5-a]pyridinyl compounds, compositions and methods of use thereof

Publications (1)

Publication Number Publication Date
SG11201901954XA true SG11201901954XA (en) 2019-04-29

Family

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Family Applications (1)

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SG11201901954XA SG11201901954XA (en) 2016-09-06 2017-09-02 8-(azetidin-1-yl)-[1,2,4]triazolo[1,5-a]pyridinyl compounds, compositions and methods of use thereof

Country Status (19)

Country Link
US (3) US20190202822A1 (en)
EP (2) EP4198036A1 (en)
JP (1) JP7050761B2 (en)
KR (1) KR20190045302A (en)
CN (1) CN109890817B (en)
AU (1) AU2017324281A1 (en)
BR (1) BR112019004486A2 (en)
CA (1) CA3035712A1 (en)
CL (1) CL2019000568A1 (en)
CO (1) CO2019002171A2 (en)
CR (1) CR20190118A (en)
IL (1) IL265153A (en)
MA (1) MA46176A (en)
MX (1) MX2019002627A (en)
PE (1) PE20190632A1 (en)
PH (1) PH12019500478A1 (en)
RU (1) RU2019109570A (en)
SG (1) SG11201901954XA (en)
WO (1) WO2018046409A1 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2020257143A1 (en) * 2019-06-18 2020-12-24 Genentech, Inc. Pyrazolopyrimidine aryl ether inhibitors of jak kinases and uses thereof
GB202213164D0 (en) 2022-09-08 2022-10-26 Cambridge Entpr Ltd Novel compounds, compositions and therapeutic uses thereof

Family Cites Families (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU650953B2 (en) 1991-03-21 1994-07-07 Novartis Ag Inhaler
US5543523A (en) 1994-11-15 1996-08-06 Regents Of The University Of Minnesota Method and intermediates for the synthesis of korupensamines
WO1997002289A1 (en) 1995-07-06 1997-01-23 Zeneca Limited Peptide inhibitors of fibronectine
US6248713B1 (en) 1995-07-11 2001-06-19 Biogen, Inc. Cell adhesion inhibitors
YU25500A (en) 1999-05-11 2003-08-29 Pfizer Products Inc. Process for the synthesis of nucleosite analogues
GB0028383D0 (en) 2000-11-21 2001-01-03 Novartis Ag Organic compounds
EP1241176A1 (en) 2001-03-16 2002-09-18 Pfizer Products Inc. Purine derivatives for the treatment of ischemia
DE60214428T2 (en) 2001-12-20 2007-09-20 Bayer Healthcare Ag 1, 4-DIHYDRO-1, 4-DIPHENYLPYRIDINE DERIVATIVES
SE0302487D0 (en) 2003-09-18 2003-09-18 Astrazeneca Ab Novel compounds
GB0502258D0 (en) 2005-02-03 2005-03-09 Argenta Discovery Ltd Compounds and their use
MX2010014005A (en) 2008-06-20 2011-02-15 Genentech Inc Triazolopyridine jak inhibitor compounds and methods.
WO2010010184A1 (en) * 2008-07-25 2010-01-28 Galapagos Nv [1, 2, 4] triazolo [1, 5-a] pyridines as jak inhibitors
US8501936B2 (en) 2009-06-05 2013-08-06 Cephalon, Inc. Preparation and uses of 1,2,4-triazolo [1,5a] pyridine derivatives
US8575336B2 (en) 2011-07-27 2013-11-05 Pfizer Limited Indazoles
ES2845210T3 (en) * 2013-05-17 2021-07-26 Incyte Corp Bipirazole derivatives as JAK inhibitors
SG11201601707PA (en) * 2013-09-05 2016-04-28 Hoffmann La Roche Triazolopyridine compounds, compositions and methods of use thereof
JP2018507236A (en) * 2015-03-04 2018-03-15 エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft Triazolopyridine compounds and methods of use thereof

Also Published As

Publication number Publication date
MX2019002627A (en) 2019-10-30
CL2019000568A1 (en) 2019-07-12
EP3510030B1 (en) 2023-03-22
CN109890817B (en) 2022-06-17
CN109890817A (en) 2019-06-14
CA3035712A1 (en) 2018-03-15
EP4198036A1 (en) 2023-06-21
RU2019109570A (en) 2020-10-08
WO2018046409A1 (en) 2018-03-15
JP2019526593A (en) 2019-09-19
MA46176A (en) 2019-07-17
AU2017324281A1 (en) 2019-03-21
US20190202822A1 (en) 2019-07-04
PH12019500478A1 (en) 2019-12-02
BR112019004486A2 (en) 2019-05-28
CR20190118A (en) 2019-04-30
JP7050761B2 (en) 2022-04-08
US20200270248A1 (en) 2020-08-27
PE20190632A1 (en) 2019-04-26
KR20190045302A (en) 2019-05-02
EP3510030A1 (en) 2019-07-17
IL265153A (en) 2019-05-30
US20230242530A1 (en) 2023-08-03
CO2019002171A2 (en) 2019-05-21
RU2019109570A3 (en) 2020-10-08

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