WO2003101489A1 - Composition medicinale utilisee dans le traitement des maladies du tube digestif - Google Patents
Composition medicinale utilisee dans le traitement des maladies du tube digestif Download PDFInfo
- Publication number
- WO2003101489A1 WO2003101489A1 PCT/JP2003/006845 JP0306845W WO03101489A1 WO 2003101489 A1 WO2003101489 A1 WO 2003101489A1 JP 0306845 W JP0306845 W JP 0306845W WO 03101489 A1 WO03101489 A1 WO 03101489A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- group
- oxazepine
- dihydro
- pyrrolidine
- dibenzo
- Prior art date
Links
Classifications
-
- 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
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- 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
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/553—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having at least one nitrogen and one oxygen as ring hetero atoms, e.g. loxapine, staurosporine
-
- 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
- A61P1/04—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
-
- 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
Definitions
- the compound [III] that can be used in the present invention has one or more asymmetric carbon atoms, and may have optical isomers. These optical isomers, arbitrary mixtures or racemates thereof are included in the compounds of the present invention. Among these, it is preferable that the configuration at the 2-position of the pyrrolidine ring or piperidine ring bonded to dihydrodibenzoxoxazepine ⁇ is R-form.
- aromatic rings G, J, K, ⁇ 3 , A, B, and D are the same as above, represents 1 or 2, and V and V 'are chlorine, bromine, iodine, and tosyloxy. And a leaving group such as a mesyloxy group, and U represents a protecting group for an amino group such as a t-butyloxycarbonyl group, a benzyloxycarbonyl group, and a tosyl group.
- the compound [V] is reacted in the presence of a base by dropwise addition of Nt-butoxycarbonyl 2-piperidylmethyl tosylate represented by the above general formula [VI I], and the like.
- compound [XVIII] can be produced by condensing compound [XIX] and compound [XX].
- the condensation reaction refers to, for example, an amidation reaction using N, N, 1-dicyclohexylcarbodiimide or N-dimethylaminopropyl-1-N'-ethylcarbodiimide, a salt thereof, and the like
- compound [XIX] Can be selected from known methods such as an acid anhydride method in which is converted to an acid anhydride and then condensation, and a method via an acid chloride or an acid bromide of the compound [XIX].
- the carrier and diluent include glucose, sucrose, lactose, talc, silica, cellulose, methylcellulose, starch, gelatin, ethylene glycol, polyethylene glycol, glycerin, ethanol, water and oils and fats. Is raised.
- the following mixture was mixed in a conventional manner, and the mixture was tableted to give tablets containing 50 mg of the active ingredient per tablet.
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Investigating Or Analysing Biological Materials (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU2003241987A AU2003241987A1 (en) | 2002-05-31 | 2003-05-30 | Medicinal composition for treatment for digestive tract disease |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2002-160188 | 2002-05-31 | ||
JP2002160188A JP2005343791A (ja) | 2002-05-31 | 2002-05-31 | 消化管疾患を治療するための医薬組成物 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2003101489A1 true WO2003101489A1 (fr) | 2003-12-11 |
Family
ID=29706537
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2003/006845 WO2003101489A1 (fr) | 2002-05-31 | 2003-05-30 | Composition medicinale utilisee dans le traitement des maladies du tube digestif |
Country Status (3)
Country | Link |
---|---|
JP (1) | JP2005343791A (fr) |
AU (1) | AU2003241987A1 (fr) |
WO (1) | WO2003101489A1 (fr) |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0404359A1 (fr) * | 1989-05-27 | 1990-12-27 | Pfizer Limited | Dérivés de dibenzothiazépines utiles comme agents antispasmodiques |
EP0889043A1 (fr) * | 1996-03-11 | 1999-01-07 | Ajinomoto Co., Inc. | DERIVES DE 5,11-DIHYDRODIBENZ b,e] 1,4]OXAZEPINE, ET COMPOSITIONS MEDICAMENTEUSES LES COMPORTANT |
EP1020466A1 (fr) * | 1997-09-10 | 2000-07-19 | Ajinomoto Co., Inc. | DERIVES DE 5,11-DIHYDRODIBENZ[b,e][1,4]OXAZEPINE ET COMPOSITIONS MEDICAMENTEUSES LES CONTENANT |
WO2001017980A1 (fr) * | 1999-09-03 | 2001-03-15 | Ajinomoto Co., Inc. | Nouveaux procedes de preparation de derives d'oxazepine |
EP1142884A1 (fr) * | 1999-01-08 | 2001-10-10 | Ajinomoto Co., Inc. | Derives d'oxazepine et medicaments contenant ces derives |
WO2002096891A1 (fr) * | 2001-05-30 | 2002-12-05 | Ajinomoto Co.,Inc. | Derives de dihydrodiaryloxazepine, et medicaments contenant ces derives |
-
2002
- 2002-05-31 JP JP2002160188A patent/JP2005343791A/ja active Pending
-
2003
- 2003-05-30 AU AU2003241987A patent/AU2003241987A1/en not_active Abandoned
- 2003-05-30 WO PCT/JP2003/006845 patent/WO2003101489A1/fr not_active Application Discontinuation
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0404359A1 (fr) * | 1989-05-27 | 1990-12-27 | Pfizer Limited | Dérivés de dibenzothiazépines utiles comme agents antispasmodiques |
EP0889043A1 (fr) * | 1996-03-11 | 1999-01-07 | Ajinomoto Co., Inc. | DERIVES DE 5,11-DIHYDRODIBENZ b,e] 1,4]OXAZEPINE, ET COMPOSITIONS MEDICAMENTEUSES LES COMPORTANT |
EP1020466A1 (fr) * | 1997-09-10 | 2000-07-19 | Ajinomoto Co., Inc. | DERIVES DE 5,11-DIHYDRODIBENZ[b,e][1,4]OXAZEPINE ET COMPOSITIONS MEDICAMENTEUSES LES CONTENANT |
EP1142884A1 (fr) * | 1999-01-08 | 2001-10-10 | Ajinomoto Co., Inc. | Derives d'oxazepine et medicaments contenant ces derives |
WO2001017980A1 (fr) * | 1999-09-03 | 2001-03-15 | Ajinomoto Co., Inc. | Nouveaux procedes de preparation de derives d'oxazepine |
WO2002096891A1 (fr) * | 2001-05-30 | 2002-12-05 | Ajinomoto Co.,Inc. | Derives de dihydrodiaryloxazepine, et medicaments contenant ces derives |
Also Published As
Publication number | Publication date |
---|---|
JP2005343791A (ja) | 2005-12-15 |
AU2003241987A1 (en) | 2003-12-19 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP4700007B2 (ja) | N−[フェニル(ピロリジン−2−イル)メチル]ベンズアミドおよびn−[(アゼパン−2−イル)フェニルメチル]ベンズアミド誘導体、この調製方法および治療法における使用 | |
SK129590A3 (en) | 3-substituted pyrolidine derivative, preparation method thereof, intermediate products of this method, pharmaceutical composition containing this derivative | |
EP0505377A1 (fr) | Antagonistes de recepteurs muscariniques. | |
FI81342C (fi) | Foerfarande foer framstaellning av farmaceutiskt vaerdefulla basiskt substituerade tricykliska diazepinoner. | |
JP3331048B2 (ja) | インドール誘導体 | |
FI94246C (fi) | Menetelmä uusien terapeuttisesti käyttökelpoisten bentsatsepiini- ja bentsotiatsepiinijohdannaisten valmistamiseksi | |
KR100340145B1 (ko) | 벤즈아제핀유도체및이의중간체화합물 | |
EP3253761A1 (fr) | Dérivés 3,3-difluoro-pipéridine en tant qu'antagonistes des récepteurs nmda nr2b | |
EP1778641A1 (fr) | Antagonistes des recepteurs 5-ht7 | |
JP4618127B2 (ja) | 1,3−ジヒドロ−2h−インドール−2−オン誘導体 | |
Sleevi et al. | Optical isomers of rocastine and close analogs: synthesis and H1 antihistaminic activity of its enantiomers and their structural relationship to the classical antihistamines | |
HUT58329A (en) | Process for producing 5,11-dihydro-dibenzo(b,e)(1,4)-thiazepine derivatives and pharmaceutical compositions containing them | |
WO2003101983A1 (fr) | Derive tetrahydropyrane | |
FI90662B (fi) | Menetelmä terapeuttisesti käyttökelpoisten 2-aminoetanolijohdannaisten valmistamiseksi | |
AU740878B2 (en) | 5,11-dihydrodibenz(b,e)(1,4)oxazepine derivatives and medicinal composition containing the same | |
WO2003101489A1 (fr) | Composition medicinale utilisee dans le traitement des maladies du tube digestif | |
CN117460729A (zh) | 作为西格玛配体的新型(高)哌啶基杂环 | |
US7320973B2 (en) | Dihydrodiaryloxazepine derivative and pharmaceutical composition containing the same | |
JP2018531949A (ja) | 疼痛に対して活性を有する置換モルホリン誘導体 | |
WO2003101490A1 (fr) | Composition de medicament contenant un antagoniste des canaux calciques | |
US6528504B2 (en) | Oxazepine derivatives and medicine containing the same | |
JP2008525512A (ja) | 5−ht7受容体拮抗薬 | |
JP2023046323A (ja) | オキサジアゾール誘導体を含有する医薬組成物 | |
CN115916790A (zh) | 作为IAP拮抗剂的吡啶并[2,3-b][1,4]噁嗪或四氢吡啶并[2,3-b][1,4]氧氮杂卓 | |
WO2003106423A1 (fr) | Amine cyclique et composition médicinale la contenant |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AK | Designated states |
Kind code of ref document: A1 Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NI NO NZ OM PH PL PT RO RU SC SD SE SG SK SL TJ TM TN TR TT TZ UA UG US UZ VC VN YU ZA ZM ZW |
|
AL | Designated countries for regional patents |
Kind code of ref document: A1 Designated state(s): GH GM KE LS MW MZ SD SL SZ TZ UG ZM ZW AM AZ BY KG KZ MD RU TJ TM AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IT LU MC NL PT RO SE SI SK TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
122 | Ep: pct application non-entry in european phase | ||
NENP | Non-entry into the national phase |
Ref country code: JP |
|
WWW | Wipo information: withdrawn in national office |
Country of ref document: JP |