CN103347882B - 作为III型受体酪氨酸激酶抑制剂的取代的N-(1H-吲唑-4-基)咪唑并[1,2-a]吡啶-3-甲酰胺化合物 - Google Patents

作为III型受体酪氨酸激酶抑制剂的取代的N-(1H-吲唑-4-基)咪唑并[1,2-a]吡啶-3-甲酰胺化合物 Download PDF

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CN103347882B
CN103347882B CN201180067342.XA CN201180067342A CN103347882B CN 103347882 B CN103347882 B CN 103347882B CN 201180067342 A CN201180067342 A CN 201180067342A CN 103347882 B CN103347882 B CN 103347882B
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methyl
pyridine
imidazo
indazole
carboxamide
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CN103347882A (zh
Inventor
M.L.博伊斯
R.K.德莱尔
E.J.希肯
A.L.肯尼迪
D.A.马里斯卡
F.P.玛姆萨特
M.C.芒森
B.纽豪斯
B.拉斯特
J.P.里齐
M.E.罗德里格兹
G.T.托帕洛夫
赵千
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Array Biopharma Inc
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Array Biopharma Inc
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    • 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
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    • 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
    • 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
    • A61K31/496Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
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    • A61P19/00Drugs for skeletal disorders
    • AHUMAN NECESSITIES
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    • A61P19/00Drugs for skeletal disorders
    • A61P19/08Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
    • AHUMAN NECESSITIES
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    • A61P25/00Drugs for disorders of the nervous system
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    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
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  • Orthopedic Medicine & Surgery (AREA)
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  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
CN201180067342.XA 2010-12-13 2011-12-13 作为III型受体酪氨酸激酶抑制剂的取代的N-(1H-吲唑-4-基)咪唑并[1,2-a]吡啶-3-甲酰胺化合物 Expired - Fee Related CN103347882B (zh)

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CN201811311712.XA CN109608449A (zh) 2010-12-13 2011-12-13 作为iii型受体酪氨酸激酶抑制剂的化合物
CN201610248287.9A CN105924437B (zh) 2010-12-13 2011-12-13 作为iii型受体酪氨酸激酶抑制剂的化合物

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US42254710P 2010-12-13 2010-12-13
US61/422,547 2010-12-13
PCT/US2011/064549 WO2012082689A1 (en) 2010-12-13 2011-12-13 SUBSTITUTED N-(1H-INDAZOL-4-YL)IMIDAZO[1,2-a]PYRIDINE-3-CARBOXAMIDE COMPOUNDS AS TYPE III RECEPTOR TYROSINE KINASE INHIBITORS

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CN201610248287.9A Division CN105924437B (zh) 2010-12-13 2011-12-13 作为iii型受体酪氨酸激酶抑制剂的化合物
CN201811311712.XA Division CN109608449A (zh) 2010-12-13 2011-12-13 作为iii型受体酪氨酸激酶抑制剂的化合物

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CN201811311712.XA Pending CN109608449A (zh) 2010-12-13 2011-12-13 作为iii型受体酪氨酸激酶抑制剂的化合物
CN201610248287.9A Expired - Fee Related CN105924437B (zh) 2010-12-13 2011-12-13 作为iii型受体酪氨酸激酶抑制剂的化合物

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CN201610248287.9A Expired - Fee Related CN105924437B (zh) 2010-12-13 2011-12-13 作为iii型受体酪氨酸激酶抑制剂的化合物

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109608449A (zh) * 2010-12-13 2019-04-12 阵列生物制药公司 作为iii型受体酪氨酸激酶抑制剂的化合物

Families Citing this family (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102822170B (zh) * 2009-12-21 2014-12-10 阵列生物制药公司 作为cFMS抑制剂的取代的N-(1H-吲唑-4-基)咪唑并[1,2-a]吡啶-3-羧酰胺化合物
GB201315486D0 (en) * 2013-08-30 2013-10-16 Ucb Pharma Sa Antibodies
JO3517B1 (ar) 2014-01-17 2020-07-05 Novartis Ag ان-ازاسبيرو الكان حلقي كبديل مركبات اريل-ان مغايرة وتركيبات لتثبيط نشاط shp2
CN104496891A (zh) * 2014-12-06 2015-04-08 哈尔滨工业大学 吡啶衍生物2-叔丁氧基-6-亚甲基氯吡啶的合成方法
CN104974078A (zh) * 2015-06-25 2015-10-14 黄荣辉 一种2-甲基-6-氯甲基吡啶盐酸盐的制备方法
WO2017024408A1 (en) 2015-08-11 2017-02-16 Neomed Institute Aryl-substituted dihydroquinolinones, their preparation and their use as pharmaceuticals
US10836742B2 (en) 2015-08-11 2020-11-17 Neomed Institute N-substituted bicyclic lactams, their preparation and their use as pharmaceuticals
CN108137539B (zh) 2015-08-12 2022-01-11 尼奥迈德研究所 取代的苯并咪唑、它们的制备和它们作为药物的用途
US10501459B2 (en) 2015-10-21 2019-12-10 Neomed Institute Substituted imidazo[1,2-a]pyridines as bromodomain inhibitors
ES2895904T3 (es) * 2015-11-02 2022-02-23 Genase Therapeutics B V Tetrahidroindazoles y usos médicos de los mismos
CN105198799A (zh) * 2015-11-03 2015-12-30 江苏梦得电镀化学品有限公司 一种2-甲基-6-氯甲基吡啶盐酸盐的制备方法
WO2017127930A1 (en) 2016-01-28 2017-08-03 Neomed Institute Substituted [1,2,4]triazolo[4,3-a]pyridines, their preparation and their use as pharmaceuticals
MX383856B (es) 2016-06-14 2025-03-14 Novartis Ag Compuestos y composiciones para inhibir la actividad de shp2.
CN106187899B (zh) * 2016-06-28 2019-07-16 绍兴文理学院 一种氟代氮杂芳烃的合成方法
WO2018019291A1 (en) * 2016-07-29 2018-02-01 The Hong Kong University Of Science And Technology C(sp3)-c(sp2) cross-coupling reaction of organozinc reagents and heterocyclic (pseudo)halides
EP3535243B1 (en) 2016-11-04 2021-12-15 Auckland Uniservices Limited Substituted 9h-xanthen-9-one, 9h-thioxanthen-9-one and acridin-9(10h)-one derivatives and related compounds csf-1r inhibitors for the treatment of cancer
CA3041986A1 (en) * 2016-11-28 2018-05-31 Eisai R&D Management Co., Ltd. Salts of indazole derivative and crystals thereof
WO2018213665A1 (en) 2017-05-19 2018-11-22 Syndax Pharmaceuticals, Inc. Combination therapies
FI3658552T3 (fi) 2017-07-28 2023-11-16 Yuhan Corp Menetelmä n-(5-((4-(4-((dimetyyliamino)metyyli)-3-fenyyli-1h-pyratsol-1-yyli)pyrimidin-2-yyli)amino)-4-metoksi-2-morfolinofenyyli)akryyliamidin valmistamiseksi saattamalla vastaava amiini reagoimaan 3-halopropionyylikloridin kanssa
KR20200143376A (ko) 2018-03-13 2020-12-23 샤이어 휴먼 지네틱 테라피즈 인크. 혈장 칼리크레인 억제제로서의 치환된 이미다조피리딘 및 이의 용도
CN111410654B (zh) * 2019-01-19 2022-05-17 江苏新元素医药科技有限公司 3-溴-5-(2-乙基咪唑并[1,2-a]吡啶-3-羰基)-2-羟基苯甲腈的合成
TWI841671B (zh) 2019-01-24 2024-05-11 日商第一三共股份有限公司 具有取代基之脲化合物
TWI759829B (zh) 2019-08-23 2022-04-01 財團法人生物技術開發中心 作為第iii型受體酪胺酸激酶抑制劑之雜環吡唑衍生物
CN114667289B (zh) 2019-09-18 2025-08-26 武田药品工业有限公司 杂芳基血浆激肽释放酶抑制剂
EP4031547B1 (en) 2019-09-18 2024-07-17 Takeda Pharmaceutical Company Limited Plasma kallikrein inhibitors and uses thereof
PH12022551401A1 (en) 2019-12-09 2023-08-23 Syndax Pharmaceuticals Inc Antibodies for the treatment of chronic graft versus host disease
TW202542157A (zh) * 2024-01-04 2025-11-01 大陸商上海翰森生物醫藥科技有限公司 多環類衍生物抑制劑、其製備方法和應用

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101679409A (zh) * 2006-12-22 2010-03-24 Astex治疗学有限公司 新颖化合物
CN101679423A (zh) * 2007-04-03 2010-03-24 阵列生物制药公司 作为受体酪氨酸激酶抑制剂的咪唑并[1,2-a]吡啶化合物
CN102822170A (zh) * 2009-12-21 2012-12-12 阵列生物制药公司 作为cFMS抑制剂的取代的N-(1H-吲唑-4-基)咪唑并[1,2-a]吡啶-3-羧酰胺化合物

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5543523A (en) 1994-11-15 1996-08-06 Regents Of The University Of Minnesota Method and intermediates for the synthesis of korupensamines
NZ537156A (en) 2002-05-23 2007-06-29 Cytopia Pty Ltd Kinase inhibitors
FR2925901B1 (fr) 2008-01-02 2011-03-04 Sanofi Aventis DERIVES DE N-HETEROCYCLIQUE-IMIDAZO°1,2-a!PYRIDINE-2- CARBOXAMIDES, LEUR PREPARATION ET LEUR APPLICATION EN THERAPEUTIQUE
JP5502076B2 (ja) * 2008-06-05 2014-05-28 グラクソ グループ リミテッド 新規化合物
TW201105669A (en) * 2009-07-30 2011-02-16 Irm Llc Compounds and compositions as Syk kinase inhibitors
JO3337B1 (ar) 2010-12-13 2019-03-13 Debiopharm Sa تركيبات صيدلية تشمل أليسبوريفير
SI2651939T1 (sl) 2010-12-13 2015-07-31 Array Biopharma, Inc. SUBSTITUIRANE N-(1H-INDAZOL-4-IL)IMIDAZO(1,2-a)PIRIDIN-3-KARBOKSAMIDNE SPOJINE KOT INHIBITORJI RECEPTORSKE TIROZINSKE KINAZE TIPA III
CN102250246A (zh) * 2011-06-10 2011-11-23 常州亚当生物技术有限公司 抗VEGF/PDGFRβ双特异性抗体及其应用

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101679409A (zh) * 2006-12-22 2010-03-24 Astex治疗学有限公司 新颖化合物
CN101679423A (zh) * 2007-04-03 2010-03-24 阵列生物制药公司 作为受体酪氨酸激酶抑制剂的咪唑并[1,2-a]吡啶化合物
CN102822170A (zh) * 2009-12-21 2012-12-12 阵列生物制药公司 作为cFMS抑制剂的取代的N-(1H-吲唑-4-基)咪唑并[1,2-a]吡啶-3-羧酰胺化合物

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109608449A (zh) * 2010-12-13 2019-04-12 阵列生物制药公司 作为iii型受体酪氨酸激酶抑制剂的化合物

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US20180086758A1 (en) 2018-03-29
KR20140014109A (ko) 2014-02-05
JP2016040303A (ja) 2016-03-24
US9809590B2 (en) 2017-11-07
HK1190709A1 (en) 2014-07-11
CA2821712C (en) 2019-02-12
AU2018201903B2 (en) 2019-09-19
AU2011344001B2 (en) 2016-06-30
US9174981B2 (en) 2015-11-03
ES2540996T3 (es) 2015-07-15
CL2013001712A1 (es) 2013-12-06
TWI527813B (zh) 2016-04-01
JP2013545808A (ja) 2013-12-26
EP2651939B1 (en) 2015-04-08
DK2651939T3 (en) 2015-06-01
BR112013014854A2 (pt) 2016-10-18
CN109608449A (zh) 2019-04-12
AU2018201903A1 (en) 2018-04-12
PH12013501221A1 (en) 2022-03-30
BR112013014854A8 (pt) 2018-03-27
PT2651939E (pt) 2015-08-04
RS54070B1 (sr) 2015-10-30
CN105924437B (zh) 2018-11-30
US10669269B2 (en) 2020-06-02
ME02172B (me) 2015-10-20
UA112425C2 (uk) 2016-09-12
AU2016222468B2 (en) 2017-12-21
MY172110A (en) 2019-11-14
US20130274244A1 (en) 2013-10-17
SMT201500165B (it) 2015-09-07
MX2013006763A (es) 2014-01-08
JP5868996B2 (ja) 2016-02-24
HUE025416T2 (en) 2016-02-29
CA2821712A1 (en) 2012-06-21
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CN103347882A (zh) 2013-10-09
BR112013014854B1 (pt) 2020-12-08
JP2018065835A (ja) 2018-04-26
WO2012082689A1 (en) 2012-06-21
IL226911A (en) 2016-09-29
CR20130349A (es) 2013-08-09
KR101974665B1 (ko) 2019-05-02
TW201305156A (zh) 2013-02-01
SG191129A1 (en) 2013-07-31
US20160002232A1 (en) 2016-01-07
RU2591195C2 (ru) 2016-07-10
CA3027814A1 (en) 2012-06-21
UY33801A (es) 2013-06-28
EP2651939A1 (en) 2013-10-23
CN105924437A (zh) 2016-09-07
AU2016222468A1 (en) 2016-09-22
SI2651939T1 (sl) 2015-07-31
HRP20150571T1 (xx) 2015-07-03
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PL2651939T3 (pl) 2015-10-30
CO6751248A2 (es) 2013-09-16

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