ATE545647T1 - 5,6,7,8-tetrahydro-imidazoä1,5-aüpyrazinderivat - Google Patents

5,6,7,8-tetrahydro-imidazoä1,5-aüpyrazinderivat

Info

Publication number: ATE545647T1
Authority: AT; Austria
Prior art keywords: alkyl; tetrahydro; alkoxy; halogen; imidazoä1
Prior art date: 2006-12-22

Application number

AT07859469T

Other languages

English (en)

Inventor

Hamed Aissaoui

Christoph Boss

Markus Gude

Ralf Koberstein

Thierry Sifferlen

Original Assignee

Actelion Pharmaceuticals Ltd

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.)

2006-12-22

Filing date

2007-12-20

Publication date

2012-03-15

2007-12-20 Application filed by Actelion Pharmaceuticals Ltd filed Critical Actelion Pharmaceuticals Ltd

2012-03-15 Application granted granted Critical

2012-03-15 Publication of ATE545647T1 publication Critical patent/ATE545647T1/de

Links

125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 6
229910052736 halogen Inorganic materials 0.000 abstract 3
150000002367 halogens Chemical class 0.000 abstract 3
125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 2
150000001875 compounds Chemical class 0.000 abstract 2
229910052739 hydrogen Inorganic materials 0.000 abstract 2
239000001257 hydrogen Substances 0.000 abstract 2
125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 2
125000006656 (C2-C4) alkenyl group Chemical group 0.000 abstract 1
WROMFHICINADER-UHFFFAOYSA-N 5,6,7,8-tetrahydroimidazo[1,5-a]pyrazine Chemical class C1NCCN2C=NC=C21 WROMFHICINADER-UHFFFAOYSA-N 0.000 abstract 1
229940123730 Orexin receptor antagonist Drugs 0.000 abstract 1
125000004849 alkoxymethyl group Chemical group 0.000 abstract 1
125000004093 cyano group Chemical group *C#N 0.000 abstract 1
-1 cyano, hydroxymethyl Chemical group 0.000 abstract 1
125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 abstract 1
239000003814 drug Substances 0.000 abstract 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
150000003839 salts Chemical class 0.000 abstract 1
125000001424 substituent group Chemical group 0.000 abstract 1
125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 abstract 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
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- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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- A61P9/12—Antihypertensives
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings

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Health & Medical Sciences (AREA)
Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Engineering & Computer Science (AREA)
Bioinformatics & Cheminformatics (AREA)
Life Sciences & Earth Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
General Chemical & Material Sciences (AREA)
Medicinal Chemistry (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Pharmacology & Pharmacy (AREA)
Animal Behavior & Ethology (AREA)
General Health & Medical Sciences (AREA)
Public Health (AREA)
Veterinary Medicine (AREA)
Neurology (AREA)
Neurosurgery (AREA)
Biomedical Technology (AREA)
Pain & Pain Management (AREA)
Cardiology (AREA)
Psychiatry (AREA)
Physical Education & Sports Medicine (AREA)
Heart & Thoracic Surgery (AREA)
Addiction (AREA)
Rheumatology (AREA)
Diabetes (AREA)
Orthopedic Medicine & Surgery (AREA)
Pulmonology (AREA)
Endocrinology (AREA)
Urology & Nephrology (AREA)
Hospice & Palliative Care (AREA)
Psychology (AREA)
Dermatology (AREA)
Hematology (AREA)
Anesthesiology (AREA)
Obesity (AREA)
Gynecology & Obstetrics (AREA)
Reproductive Health (AREA)
Otolaryngology (AREA)
Emergency Medicine (AREA)

AT07859469T 2006-12-22 2007-12-20 5,6,7,8-tetrahydro-imidazoä1,5-aüpyrazinderivat ATE545647T1 (de)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
IB2006055019		2006-12-22
PCT/IB2007/055245 WO2008078291A1 (en)	2006-12-22	2007-12-20	5,6,7,8-tetrahydro-imidazo[1,5-a]pyrazine derivatives

Publications (1)

Publication Number	Publication Date
ATE545647T1 true ATE545647T1 (de)	2012-03-15

Family

ID=39273168

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
AT07859469T ATE545647T1 (de)	2006-12-22	2007-12-20	5,6,7,8-tetrahydro-imidazoä1,5-aüpyrazinderivat

Country Status (15)

Country	Link
US (1)	US8188082B2 (de)
EP (1)	EP2125823B1 (de)
JP (1)	JP2010513466A (de)
KR (1)	KR20090106538A (de)
CN (1)	CN101568542B (de)
AT (1)	ATE545647T1 (de)
AU (1)	AU2007337659A1 (de)
BR (1)	BRPI0720522A2 (de)
CA (1)	CA2669561A1 (de)
ES (1)	ES2380391T3 (de)
MA (1)	MA31002B1 (de)
MX (1)	MX2009006553A (de)
NO (1)	NO20092715L (de)
RU (1)	RU2009127842A (de)
WO (1)	WO2008078291A1 (de)

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* Cited by examiner, † Cited by third party
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CA2669561A1 (en)	2006-12-22	2008-07-03	Actelion Pharmaceuticals Ltd	5,6,7,8-tetrahydro-imidazo[1,5-a]pyrazine derivatives
US7775298B2 (en)	2007-10-29	2010-08-17	Abergeldie Holdings Pty Ltd/Abergeldie Plant Pty Ltd	Drilling assemblies and methods of drilling
CN101468988A (zh) *	2007-12-26	2009-07-01	上海恒瑞医药有限公司	哌嗪类衍生物,其制备方法及其在医药上的应用
KR20110036069A (ko) *	2008-06-25	2011-04-06	액테리온 파마슈티칼 리미티드	5,6,7,8-테트라히드로-이미다조[1,5-ａ]피라진 화합물
MX2012004753A (es)	2009-10-23	2012-09-07	Janssen Pharmaceutica Nv	Octahidropirrolo[3,4-c]pirrolos disustituidos como moduladores del receptor de orexina.
CN102258508A (zh) *	2011-04-14	2011-11-30	威海迪素制药有限公司	芳基丙烯酸衍生物抗癫痫的用途
US9440982B2 (en)	2012-02-07	2016-09-13	Eolas Therapeutics, Inc.	Substituted prolines/piperidines as orexin receptor antagonists
RU2014136339A (ru)	2012-02-07	2016-03-27	Иолас Терапьютикс, Инк.	Замещенные пролины/пиперидины как антагонисты орексиновых рецепторов
CN103980281B (zh) *	2014-05-27	2016-06-08	天津市斯芬克司药物研发有限公司	一种咪唑吡嗪化合物及其制备方法
EP3180332B1 (de)	2014-08-13	2021-10-27	Eolas Therapeutics Inc.	Difluorpyrrolidine als orexinrezeptormodulatoren
KR102738491B1 (ko)	2016-02-12	2024-12-03	아스트라제네카 아베	오렉신 수용체 조정제로서의 할로-치환된 피페리딘
RS63296B1 (sr)	2016-03-10	2022-07-29	Janssen Pharmaceutica Nv	Metode lečenja depresije korišćenjem antagonista receptora oreksin-2
CN105753788A (zh) *	2016-04-08	2016-07-13	西南科技大学	一种1-取代-2-苯基-4-碘咪唑的制备方法
US20190151304A1 (en)	2016-05-10	2019-05-23	Inserm (Institut National De La Santé Et De La Rechercjae Médicale	Methods and pharmaceutical compositions for the treatment of autoimmune inflammatory
MY202326A (en)	2017-09-14	2024-04-24	Daiichi Sankyo Co Ltd	Compound having cyclic structure
CN108101930B (zh) *	2017-12-22	2020-10-30	武汉大学	一类含有苯并噻二唑并噻吩单元的小分子受体材料及其制备方法与应用
BR112020019824A2 (pt) *	2018-03-29	2021-01-05	Board Of Regents, The University Of Texas System	Composto de fórmula estrutural i ou um sal do mesmo, composição farmacêutica, método de inibição de cbp, método de inibição de p300, método de tratamento de uma doença mediada por cbp, método de tratamento de uma doença mediada por p300 e método para alcançar um efeito em um paciente
WO2019195846A1 (en)	2018-04-06	2019-10-10	Board Of Regents, The University Of Texas System	Imidazopiperazinone inhibitors of transcription activating proteins
GB201908511D0 (en)	2019-06-13	2019-07-31	Adorx Therapeutics Ltd	Hydroxamate compounds
AU2021355480B2 (en) *	2020-10-02	2026-03-05	Board Of Regents, The University Of Texas System	Imidazopiperazine inhibitors of transcription activating proteins
EP4221708A4 (de)	2020-10-02	2024-11-06	Board of Regents, The University of Texas System	Imidazopiperazinhemmer von transkriptionsaktivierenden proteinen
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2007
- 2007-12-20 CA CA002669561A patent/CA2669561A1/en not_active Abandoned
- 2007-12-20 JP JP2009542373A patent/JP2010513466A/ja active Pending
- 2007-12-20 EP EP07859469A patent/EP2125823B1/de active Active
- 2007-12-20 ES ES07859469T patent/ES2380391T3/es active Active
- 2007-12-20 KR KR1020097015261A patent/KR20090106538A/ko not_active Ceased
- 2007-12-20 CN CN2007800478100A patent/CN101568542B/zh not_active Expired - Fee Related
- 2007-12-20 RU RU2009127842/04A patent/RU2009127842A/ru not_active Application Discontinuation
- 2007-12-20 AT AT07859469T patent/ATE545647T1/de active
- 2007-12-20 US US12/520,693 patent/US8188082B2/en not_active Expired - Fee Related
- 2007-12-20 WO PCT/IB2007/055245 patent/WO2008078291A1/en not_active Ceased
- 2007-12-20 BR BRPI0720522-8A patent/BRPI0720522A2/pt not_active IP Right Cessation
- 2007-12-20 AU AU2007337659A patent/AU2007337659A1/en not_active Abandoned
- 2007-12-20 MX MX2009006553A patent/MX2009006553A/es not_active Application Discontinuation
2009
- 2009-06-17 MA MA32006A patent/MA31002B1/fr unknown
- 2009-07-20 NO NO20092715A patent/NO20092715L/no not_active Application Discontinuation

Also Published As

Publication number	Publication date
MA31002B1 (fr)	2009-12-01
ES2380391T3 (es)	2012-05-11
KR20090106538A (ko)	2009-10-09
US20100093740A1 (en)	2010-04-15
CN101568542A (zh)	2009-10-28
BRPI0720522A2 (pt)	2014-01-07
MX2009006553A (es)	2009-06-26
AU2007337659A1 (en)	2008-07-03
WO2008078291A1 (en)	2008-07-03
US8188082B2 (en)	2012-05-29
RU2009127842A (ru)	2011-01-27
NO20092715L (no)	2009-07-20
EP2125823B1 (de)	2012-02-15
JP2010513466A (ja)	2010-04-30
CA2669561A1 (en)	2008-07-03
CN101568542B (zh)	2013-03-27
EP2125823A1 (de)	2009-12-02

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