DZ2551A1 - Forme polymorphe d'un antagoniste de récepteur tachykinine. - Google Patents

Forme polymorphe d'un antagoniste de récepteur tachykinine.

Info

Publication number: DZ2551A1
Authority: DZ; Algeria
Prior art keywords: phenyl; polymorphic form; receptor antagonist; tachykinin receptor; triazolo
Prior art date: 1997-07-02

Application number

DZ980161A

Other languages

English (en)

Inventor

Louis Crocker

James Mccauley

Original Assignee

Merck & Co Inc

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.)

1997-07-02

Filing date

1998-07-01

Publication date

2003-08-15

1998-01-07 Priority claimed from GBGB9800216.5A external-priority patent/GB9800216D0/en

1998-07-01 Application filed by Merck & Co Inc filed Critical Merck & Co Inc

2003-08-15 Application granted granted Critical

2003-08-15 Publication of DZ2551A1 publication Critical patent/DZ2551A1/fr

Links

239000002462 tachykinin receptor antagonist Substances 0.000 title abstract 2
SJRJJKPEHAURKC-UHFFFAOYSA-N N-Methylmorpholine Chemical compound CN1CCOCC1 SJRJJKPEHAURKC-UHFFFAOYSA-N 0.000 abstract 2
206010065390 Inflammatory pain Diseases 0.000 abstract 1
208000019695 Migraine disease Diseases 0.000 abstract 1
206010047700 Vomiting Diseases 0.000 abstract 1
208000006673 asthma Diseases 0.000 abstract 1
210000003169 central nervous system Anatomy 0.000 abstract 1
150000001875 compounds Chemical class 0.000 abstract 1
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
208000035475 disorder Diseases 0.000 abstract 1
208000027866 inflammatory disease Diseases 0.000 abstract 1
206010027599 migraine Diseases 0.000 abstract 1
239000008194 pharmaceutical composition Substances 0.000 abstract 1
230000002265 prevention Effects 0.000 abstract 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D265/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom and one oxygen atom as the only ring hetero atoms
- C07D265/28—1,4-Oxazines; Hydrogenated 1,4-oxazines
- C07D265/30—1,4-Oxazines; Hydrogenated 1,4-oxazines not condensed with other rings
- C07D265/32—1,4-Oxazines; Hydrogenated 1,4-oxazines not condensed with other rings with oxygen atoms directly attached to ring carbon atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/08—Drugs for disorders of the alimentary tract or the digestive system for nausea, cinetosis or vertigo; Antiemetics
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/04—Centrally acting analgesics, e.g. opioids
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Landscapes

Health & Medical Sciences (AREA)
Organic Chemistry (AREA)
Chemical & Material Sciences (AREA)
Bioinformatics & Cheminformatics (AREA)
Engineering & Computer Science (AREA)
Veterinary Medicine (AREA)
Medicinal Chemistry (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
General Chemical & Material Sciences (AREA)
Pharmacology & Pharmacy (AREA)
Life Sciences & Earth Sciences (AREA)
Animal Behavior & Ethology (AREA)
General Health & Medical Sciences (AREA)
Public Health (AREA)
Chemical Kinetics & Catalysis (AREA)
Biomedical Technology (AREA)
Neurology (AREA)
Neurosurgery (AREA)
Pulmonology (AREA)
Psychiatry (AREA)
Pain & Pain Management (AREA)
Hospice & Palliative Care (AREA)
Otolaryngology (AREA)
Rheumatology (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Polyamides (AREA)
Polyurethanes Or Polyureas (AREA)
Plural Heterocyclic Compounds (AREA)
Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

DZ980161A 1997-07-02 1998-07-01 Forme polymorphe d'un antagoniste de récepteur tachykinine. DZ2551A1 (fr)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US5160097P	1997-07-02	1997-07-02
GBGB9800216.5A GB9800216D0 (en)	1998-01-07	1998-01-07	Polymorphic form of a tachykinin receptor antagonist

Publications (1)

Publication Number	Publication Date
DZ2551A1 true DZ2551A1 (fr)	2003-08-15

Family

ID=26312895

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DZ980161A DZ2551A1 (fr)	1997-07-02	1998-07-01	Forme polymorphe d'un antagoniste de récepteur tachykinine.

Country Status (26)

Country	Link
EP (1)	EP0994867B1 (fr)
JP (1)	JP2000513383A (fr)
KR (1)	KR20010020593A (fr)
CN (1)	CN1106390C (fr)
AT (1)	ATE372991T1 (fr)
AU (1)	AU735230B2 (fr)
BG (1)	BG64703B1 (fr)
CA (1)	CA2293836C (fr)
CZ (1)	CZ295410B6 (fr)
DE (1)	DE69838421D1 (fr)
DZ (1)	DZ2551A1 (fr)
EA (1)	EA002405B1 (fr)
EE (1)	EE04152B1 (fr)
HR (1)	HRP980370B1 (fr)
HU (1)	HU228003B1 (fr)
ID (1)	ID23191A (fr)
IL (1)	IL133357A (fr)
IS (1)	IS2617B (fr)
NO (1)	NO316893B1 (fr)
NZ (1)	NZ501589A (fr)
PE (1)	PE86499A1 (fr)
PL (1)	PL191496B1 (fr)
SK (1)	SK285644B6 (fr)
TR (1)	TR199903299T2 (fr)
TW (1)	TW577887B (fr)
WO (1)	WO1999001444A1 (fr)

Families Citing this family (25)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP2003513095A (ja)	1999-10-29	2003-04-08	メルクエンドカムパニーインコーポレーテッド	タキキニン受容体アンタゴニストの多形
GB0203061D0 (en) *	2002-02-08	2002-03-27	Novartis Ag	Organic compounds
US7192962B2 (en) *	2002-05-31	2007-03-20	Schering Corporation	Xanthine phosphodiesterase V inhibitor polymorphs
GB0417702D0 (en) *	2004-08-09	2004-09-08	Merck Sharp & Dohme	New uses
EP2266980A1 (fr) *	2005-10-05	2010-12-29	Ranbaxy Laboratories Limited	Forme polymorphe d'un produit intermédiaire de l'aprepitant
EP1984359A1 (fr)	2006-02-03	2008-10-29	Glenmark Pharmaceuticals Limited	Formes amorphes et cristallines d'aprépitant et procédés pour leur préparation
EP2662374A1 (fr)	2006-04-05	2013-11-13	OPKO Health, Inc.	Sels d'hydrochlorure de 8-[{1-(3,5-bis-(trifluoromethyl) phenyl) -ethoxy}-methyl]-8-phenyl-1,7-diaza-spiro[4.5]decan-2-one et leur procédé de préparation
US20090149462A1 (en) *	2006-08-28	2009-06-11	Hetero Drugs Limited	Process for purification of aprepitant
WO2008044102A1 (fr) *	2006-10-13	2008-04-17	Glenmark Pharmaceuticals Limited	Forme polymorphe d'aprépitant et procédé de préparation de celle-ci
JP2010516731A (ja)	2007-01-24	2010-05-20	グラクソグループリミテッド	２−メトキシ−５−（５−トリフルオロメチル−テトラゾール−１−イル）−ベンジル］−（２ｓ−フェニル−ピペリジン−３ｓ−イル）−アミンを含む医薬組成物
KR20110008166A (ko) *	2008-02-18	2011-01-26	라보라토리오스 델 드라. 에스테브.에스.에이.	화학요법의 결과로 발생하는 신경병적 통증의 치료를 위한 시그마 수용체 리간드에 결합하는 화합물들의 용도
EP2116539A1 (fr)	2008-04-25	2009-11-11	Laboratorios Del. Dr. Esteve, S.A.	1-aryl-3-aminoalkoxy-pyrazoles en tant que ligands améliorant les effets analgésiques des opioïdes et réduisant leur dépendance
EP2353591A1 (fr)	2010-02-04	2011-08-10	Laboratorios Del. Dr. Esteve, S.A.	Ligands sigma pour la potentialisation de l'effet analgésique d'opioïdes et d'opiacés dans la douleur post-opératoire et en atténuant la dépendance
EP2353598A1 (fr)	2010-02-04	2011-08-10	Laboratorios Del. Dr. Esteve, S.A.	Ligands sigma pour utilisation dans la prévention et/ou le traitement de la douleur post-opératoire
EP2388005A1 (fr)	2010-05-21	2011-11-23	Laboratorios Del. Dr. Esteve, S.A.	Ligands sigma pour la prévention et/ou le traitement du vomissement induit par la chimiothérapie ou la radiothérapie
EP2415471A1 (fr)	2010-08-03	2012-02-08	Laboratorios Del. Dr. Esteve, S.A.	Utilisation de ligands sigma dans l'hyperalgie induite par opioïdes
EP2524694A1 (fr)	2011-05-19	2012-11-21	Laboratorios Del. Dr. Esteve, S.A.	Utilisation de ligands sigma dans la douleur liée au diabète de type 2
CA2837453C (fr) *	2011-06-30	2017-04-11	Toray Industries, Inc.	Cristaux de derive de glycine et utilisation pharmaceutique de ceux-ci
CN103030668B (zh) *	2011-10-09	2016-06-15	江苏豪森药业集团有限公司	一种制备福沙匹坦二甲葡胺的方法
CZ304770B6 (cs)	2012-03-13	2014-10-08	Zentiva, K.S.	Způsob výroby 3-(((2R,3S)-2-((R)-1-(3,5-bis(trifluormethyl)fenyl)ethoxy)-3-(4-fluorfenyl)morfolino)methyl)-1H-1,2,4-triazol-5(4H)-onu (Aprepitantu) v polymorfní formě II
CN102850339B (zh) *	2012-10-17	2014-10-15	上海博志研新药物技术有限公司	一种神经激肽(nk-1)受体拮抗剂晶型制备方法
CN103288813A (zh) *	2013-06-04	2013-09-11	四川百利药业有限责任公司	一种阿瑞匹坦的制备方法
TW201607538A (zh)	2013-12-17	2016-03-01	以斯提夫博士實驗室股份有限公司	血清素－去甲腎上腺素再攝取抑制劑（ＳＮＲＩＳ）和σ受體配體組合物
CN104119325B (zh) *	2014-07-15	2017-03-22	中山奕安泰医药科技有限公司	阿瑞吡坦多晶型物的制备方法
CN105837526B (zh) *	2016-01-22	2018-02-27	浙江工业大学	一种阿瑞吡坦重要合成中间体(2s,3r)‑4‑苄基‑3‑(4‑氟苯基)吗啉‑2‑醇的制备方法

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
IL111960A (en) *	1993-12-17	1999-12-22	Merck & Co Inc	Morpholines and thiomorpholines their preparation and pharmaceutical compositions containing them

1998
- 1998-07-01 TR TR1999/03299T patent/TR199903299T2/xx unknown
- 1998-07-01 EA EA199901114A patent/EA002405B1/ru not_active IP Right Cessation
- 1998-07-01 CZ CZ19994777A patent/CZ295410B6/cs not_active IP Right Cessation
- 1998-07-01 EP EP98933088A patent/EP0994867B1/fr not_active Expired - Lifetime
- 1998-07-01 CA CA002293836A patent/CA2293836C/fr not_active Expired - Lifetime
- 1998-07-01 HU HU0004008A patent/HU228003B1/hu not_active IP Right Cessation
- 1998-07-01 SK SK1872-99A patent/SK285644B6/sk not_active IP Right Cessation
- 1998-07-01 AU AU82833/98A patent/AU735230B2/en not_active Expired
- 1998-07-01 CN CN98806703A patent/CN1106390C/zh not_active Expired - Lifetime
- 1998-07-01 EE EEP199900603A patent/EE04152B1/xx unknown
- 1998-07-01 HR HR980370A patent/HRP980370B1/xx not_active IP Right Cessation
- 1998-07-01 TW TW087110655A patent/TW577887B/zh not_active IP Right Cessation
- 1998-07-01 DZ DZ980161A patent/DZ2551A1/fr active
- 1998-07-01 KR KR1019997012571A patent/KR20010020593A/ko not_active Ceased
- 1998-07-01 AT AT98933088T patent/ATE372991T1/de not_active IP Right Cessation
- 1998-07-01 DE DE69838421T patent/DE69838421D1/de not_active Expired - Lifetime
- 1998-07-01 PL PL337579A patent/PL191496B1/pl unknown
- 1998-07-01 NZ NZ501589A patent/NZ501589A/en not_active IP Right Cessation
- 1998-07-01 IL IL13335798A patent/IL133357A/xx not_active IP Right Cessation
- 1998-07-01 JP JP11507368A patent/JP2000513383A/ja active Pending
- 1998-07-01 WO PCT/US1998/013766 patent/WO1999001444A1/fr not_active Ceased
- 1998-07-01 ID IDW991716A patent/ID23191A/id unknown
- 1998-07-02 PE PE1998000593A patent/PE86499A1/es not_active IP Right Cessation
1999
- 1999-12-10 IS IS5293A patent/IS2617B/is unknown
- 1999-12-14 BG BG104010A patent/BG64703B1/bg unknown
- 1999-12-29 NO NO19996549A patent/NO316893B1/no not_active IP Right Cessation

Also Published As

Publication number	Publication date
SK285644B6 (sk)	2007-05-03
TR199903299T2 (xx)	2000-07-21
NO996549L (no)	2000-03-01
EE9900603A (et)	2000-08-15
CA2293836A1 (fr)	1999-01-14
SK187299A3 (en)	2000-07-11
NO316893B1 (no)	2004-06-14
WO1999001444A1 (fr)	1999-01-14
KR20010020593A (ko)	2001-03-15
HUP0004008A3 (en)	2002-03-28
AU735230B2 (en)	2001-07-05
CA2293836C (fr)	2007-06-05
EE04152B1 (et)	2003-10-15
IS5293A (is)	1999-12-10
IS2617B (is)	2010-04-15
EP0994867A1 (fr)	2000-04-26
IL133357A (en)	2003-12-10
HRP980370A2 (en)	1999-04-30
ATE372991T1 (de)	2007-09-15
PE86499A1 (es)	1999-10-25
BG64703B1 (bg)	2005-12-30
HUP0004008A2 (hu)	2002-02-28
JP2000513383A (ja)	2000-10-10
HK1029345A1 (en)	2001-03-30
DE69838421D1 (en)	2007-10-25
ID23191A (id)	2000-03-23
PL191496B1 (pl)	2006-05-31
CZ477799A3 (cs)	2000-09-13
EP0994867B1 (fr)	2007-09-12
EA002405B1 (ru)	2002-04-25
HRP980370B1 (en)	2002-10-31
PL337579A1 (en)	2000-08-28
CN1261882A (zh)	2000-08-02
CN1106390C (zh)	2003-04-23
IL133357A0 (en)	2001-04-30
HU228003B1 (en)	2012-08-28
EA199901114A1 (ru)	2000-08-28
TW577887B (en)	2004-03-01
NO996549D0 (no)	1999-12-29
NZ501589A (en)	2001-10-26
BG104010A (en)	2001-08-31
CZ295410B6 (cs)	2005-08-17
AU8283398A (en)	1999-01-25

Publication	Publication Date	Title
ZA985765B (en)	1999-08-04	Polymorphic form of a tachykinin receptor antagonist.
NO996549L (no)	2000-03-01	Polymorf form av takykininreseptorantagonisten 2-(R)-(1-(R)-
MY155911A (en)	2015-12-15	Pharmaceutical composition of a tachykinin receptor antagonist
IL114474A (en)	1999-12-31	(R)-(3)-3-(1H-indol-3-yl)-1-[N-(2-methoxybenzyl)acetylamino]-2-[N-(2-(4-piperidin-1-yl)piperidin-1-yl acetyl)amino]propane dihydrochloride trihydrate and tachykinin receptor antagonistic pharmaceutical compositions containing it
CA2335012A1 (fr)	2000-02-17	Compositions pharmaceutiques de prevention et de traitement de troubles du systeme nerveux central
AU3401797A (en)	1998-01-07	Compounds having effects on serotonin-related systems
DK1049703T3 (da)	2003-06-02	N-[2-(5-benzyloxycarbonyl-amino-6-oxo-2--(4-fluorphenyl)-1,6-dihydro-1-pyrimidinyl)acetoxyl]-L-asparaginsyrealdehyd som en in vivo inhibitor af interleukin-1beta konverterende enzym
WO2003105840A3 (fr)	2004-03-25	Inhibiteurs de sphingosine kinase
MXPA02012101A (es)	2003-04-25	Procedimiento para la sintesis de 2r, 2-alpha-r, 3a)-2-[1-(3, 5 -bis(trifluorometil)phenil)etoxi]-3-(4-fluorofenil)-1,4-oxazina
PL350568A1 (en)	2002-12-16	N-(2-phenyl-4-aminobutyl)-1-naphtamides as antagonists of neurokinin 1 receptors
BR9812085A (pt)	2000-09-26	"método para a sìntese de derivados de quinolina"
AR026288A1 (es)	2003-02-05	Forma polimorfica de un antagonista del receptor de taquicinina
MY126509A (en)	2006-10-31	Polymorphic form of a tachykinin receptor antagonist
AU2001269749A1 (en)	2001-12-24	Trans-glycosidation process for the synthesis of (2r, 2-alpha-r, 3a)-2-(1-(3,5-bis(trifluoromethyl)phenyl) ethoxy)-3-(4-fluorophenyl)-1,4-oxazine
WO2002024727A3 (fr)	2002-12-19	Nouveaux inhibiteurs de la formation de fibrilles d'iapp et utilisations associees
CA2262267A1 (fr)	1999-08-20	Compositions pharmaceutiques contre la migraine et methode d'utilisation
ECSP982575A (es)	1999-04-13	Forma polimorfica de un antagonista de receptor de taquiquinina
NO993372D0 (no)	1999-07-08	Substituerte 4-(6-fluor-(1H)-indol-3-yl)-1,2,3,6-tetrahydropyridin for behandling av CNS-forstyrrelser
ECSP003740A (es)	2000-12-19	Forma polimorfica de un antagonista de receptor de taquiquinina
BR9810360A (pt)	2001-01-30	Forma polimórfica do composto 2-(r)-(1-(r) - (3,5-bis(tri-fluorometil)fenil)etoxi) -3-(s) - (4-fluoro) fenil-4(3- (5-oxo-1h,4h-1,2,4-triazolo) metilmorfolino, processo para preparação da forma 1 do mesmo, composição farmacêutica, processo para antagonizar o efeito da substância p em seu sìtio receptor ou para o bloqueio dos receptores da neurocinina-1 em um mamìfero, processos para tratar ou prevenir uma condição selecionada, a êmese, um distúrbio do sistema nervoso central, a depressão, a ansiedade, e esquizofrenia em um mamìfero, e produto
TH17690B (th)	2004-09-23	รูปแบบโพลีมอร์ฟิกของยาต้านฤทธิ์ตัวรับของแทกกีคินิน
TH47996A (th)	2001-10-29	รูปแบบโพลีมอร์ฟิกของยาต้านฤทธิ์ตัวรับของแทกกีคินิน
MX9700960A (es)	1997-05-31	Procedimientos e intermedios en la sintesis de 5-(3-[exobiciclo[2.2.i] hept-2-iloxi]-4-metoxifenil)-3,4,5,6-tetrahidropirimidin-2(ih)-ona.