CU24000B1 - Un derivado 2-carboxamida-cicloamino-urea-tiazol-piridilo - Google Patents

Un derivado 2-carboxamida-cicloamino-urea-tiazol-piridilo

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Publication number
CU24000B1
CU24000B1 CU2011000052A CU20110052A CU24000B1 CU 24000 B1 CU24000 B1 CU 24000B1 CU 2011000052 A CU2011000052 A CU 2011000052A CU 20110052 A CU20110052 A CU 20110052A CU 24000 B1 CU24000 B1 CU 24000B1
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CU
Cuba
Prior art keywords
cicloamino
piridilo
carboxamida
tiazol
urea
Prior art date
Application number
CU2011000052A
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English (en)
Other versions
CU20110052A7 (es
Inventor
Giorgio Caravatti
Robin Alec Fairhurst
Pascal Furet
Vito Guagnano
Patricia Imbach
Original Assignee
Novartis Ag
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Publication date
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First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=40350060&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=CU24000(B1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Novartis Ag filed Critical Novartis Ag
Publication of CU20110052A7 publication Critical patent/CU20110052A7/es
Publication of CU24000B1 publication Critical patent/CU24000B1/es

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic 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
    • C07D417/14—Heterocyclic 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 three or more hetero rings
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    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/425—Thiazoles
    • A61K31/427—Thiazoles not condensed and containing further heterocyclic rings
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    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic 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
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439—Non 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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Abstract

La presente invención se refiere al compuesto (S)-1-({4-metil-5-[2-(2,2,2-trifluoro-1,1-dimetil-etil)-piridin-4-il]-tiazol-2-il}-amida de 2-amida del ácido pirrolidin-1,2-dicarboxílico de la fórmula I: útil en el tratamiento de enfermedades que mejoran mediante la inhibición de la cinasa de fosfatidil-inositol-3.
CU2011000052A 2008-09-10 2011-03-10 Un derivado 2-carboxamida-cicloamino-urea-tiazol-piridilo CU24000B1 (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP08164104 2008-09-10
US9667408P 2008-09-12 2008-09-12
PCT/EP2009/061644 WO2010029082A1 (en) 2008-09-10 2009-09-08 Organic compounds

Publications (2)

Publication Number Publication Date
CU20110052A7 CU20110052A7 (es) 2011-12-28
CU24000B1 true CU24000B1 (es) 2014-06-27

Family

ID=40350060

Family Applications (1)

Application Number Title Priority Date Filing Date
CU2011000052A CU24000B1 (es) 2008-09-10 2011-03-10 Un derivado 2-carboxamida-cicloamino-urea-tiazol-piridilo

Country Status (50)

Country Link
US (4) US8227462B2 (es)
EP (1) EP2331537B1 (es)
JP (1) JP5486601B2 (es)
KR (1) KR101290844B1 (es)
CN (1) CN102149711B (es)
AR (2) AR073369A1 (es)
AU (1) AU2009290904B2 (es)
BR (1) BRPI0918750B8 (es)
CA (1) CA2734819C (es)
CL (1) CL2011000504A1 (es)
CO (1) CO6351738A2 (es)
CR (1) CR20110059A (es)
CU (1) CU24000B1 (es)
CY (2) CY1117078T1 (es)
DK (1) DK2331537T3 (es)
DO (1) DOP2011000070A (es)
EA (1) EA018863B1 (es)
EC (1) ECSP11010880A (es)
ES (1) ES2560673T3 (es)
FI (1) FIC20200046I1 (es)
GE (1) GEP20135991B (es)
HN (1) HN2011000699A (es)
HR (1) HRP20160014T1 (es)
HU (2) HUE025884T2 (es)
IL (1) IL210976A (es)
JO (1) JO3121B1 (es)
LT (1) LTC2331537I2 (es)
LU (1) LUC00186I2 (es)
MA (1) MA32604B1 (es)
ME (1) ME01284B (es)
MX (1) MX2011002597A (es)
MY (1) MY151556A (es)
NI (1) NI201100049A (es)
NL (1) NL301071I2 (es)
NO (1) NO2020037I1 (es)
NZ (1) NZ590754A (es)
PA (1) PA8841901A1 (es)
PE (1) PE20110796A1 (es)
PL (1) PL2331537T3 (es)
PT (1) PT2331537E (es)
RS (1) RS54476B1 (es)
SI (1) SI2331537T1 (es)
SM (1) SMP201100019B (es)
SV (1) SV2011003853A (es)
TN (1) TN2011000053A1 (es)
TW (1) TWI453206B (es)
UA (1) UA104147C2 (es)
UY (1) UY32096A (es)
WO (1) WO2010029082A1 (es)
ZA (1) ZA201100699B (es)

Families Citing this family (111)

* Cited by examiner, † Cited by third party
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TW200519106A (en) * 2003-05-02 2005-06-16 Novartis Ag Organic compounds
KR20110028651A (ko) 2008-07-11 2011-03-21 노파르티스 아게 (ａ) 포스포이노시타이드 3-키나제 억제제 및 (ｂ) ｒａｓ/ｒａｆ/ｍｅｋ 경로의 조절제의 조합물
UA104147C2 (uk) 2008-09-10 2014-01-10 Новартис Аг Похідна піролідиндикарбонової кислоти та її застосування у лікуванні проліферативних захворювань
US8293753B2 (en) * 2009-07-02 2012-10-23 Novartis Ag Substituted 2-carboxamide cycloamino ureas
AR082418A1 (es) 2010-08-02 2012-12-05 Novartis Ag Formas cristalinas de 1-(4-metil-5-[2-(2,2,2-trifluoro-1,1-dimetil-etil)-piridin-4-il]-tiazol-2-il)-amida de 2-amida del acido (s)-pirrolidin-1,2-dicarboxilico
AU2015203865B2 (en) * 2010-11-08 2016-11-03 Novartis Ag Use of 2-carboxamide cycloamino urea derivatives in the treatment of EGFR dependent diseases or diseases that have acquired resistance to agents that target EGFR family members
CA2815492C (en) * 2010-11-08 2019-04-09 Novartis Ag Use of 2-carboxamide cycloamino urea derivatives in the treatment of egfr dependent diseases or diseases that have acquired resistance to agents that target egfr family members
UA112539C2 (uk) * 2011-03-03 2016-09-26 Новартіс Аг Спосіб одержання похідних 2-карбоксамідциклоаміносечовини
PE20140601A1 (es) * 2011-04-25 2014-05-24 Novartis Ag COMBINACION DE UN INHIBIDOR DE CINASA DE FOSFATIDIL-INOSITOL-3 (PI3K) Y UN INHIBIDOR DE mTOR
US9006270B2 (en) 2011-06-21 2015-04-14 Novartis Ag Polymorphs of (S)-pyrrolidine-1,2-dicarboxylic acid 2-amide 1-({4-methyl-5-[2-(2,2,2-trifluoro-1,1-dimethyl-ethyl)-pyridin-4-yl]-thiazol-2-yl}-amide
CN103635189B (zh) * 2011-07-01 2016-05-04 诺华股份有限公司 用于治疗癌症的含有cdk4/6抑制剂和pi3k抑制剂的联合治疗
CN103764144B (zh) * 2011-08-31 2016-07-20 诺华股份有限公司 Pi3k抑制剂与mek抑制剂的协同组合
WO2013049581A1 (en) * 2011-09-30 2013-04-04 Beth Israel Deaconess Medical Center Inc. Compositions and methods for the treatment of proliferative diseases
MX2014004559A (es) * 2011-10-14 2014-08-01 Novartis Ag Derivados de 2-carboxamida cicloamino urea en combinacion con inhibidores de hsp90 para el tratamiento de enfermedades proliferativas.
KR20140096035A (ko) * 2011-10-28 2014-08-04 노파르티스 아게 위장 기질 종양을 치료하는 방법
CA2853582A1 (en) 2011-11-02 2013-05-10 Novartis Ag 2-carboxamide cycloamino urea derivatives for use in treating vegf - dependent diseases
EP2817292B1 (en) * 2012-02-22 2019-12-18 Sanford-Burnham Medical Research Institute Sulfonamide compounds and uses as tnap inhibitors
MX2014011682A (es) 2012-03-29 2015-01-22 Novartis Ag Diagnostico farmaceutico.
WO2013148912A1 (en) 2012-03-30 2013-10-03 Novartis Ag Compounds for use in the treatment of neuroblastoma, ewing's sarcoma or rhabdomyosarcoma
JP6301316B2 (ja) 2012-05-23 2018-03-28 エフ．ホフマン−ラ ロシュ アーゲーＦ． Ｈｏｆｆｍａｎｎ−Ｌａ Ｒｏｃｈｅ Ａｋｔｉｅｎｇｅｓｅｌｌｓｃｈａｆｔ 内胚葉細胞および肝実質細胞の組成物ならびにそれらの細胞を入手および使用する方法
US8980259B2 (en) 2012-07-20 2015-03-17 Novartis Ag Combination therapy
TR201904980T4 (tr) 2012-08-07 2019-05-21 Novartis Ag Bir B-Raf inhibitörü, bir EGFR inhibitörü ve isteğe bağlı olarak bir PI3K-alfa inhibitörü içeren farmasötik kombinasyonlar.
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