KR910018368A - 카르복실산 유도체 - Google Patents
카르복실산 유도체 Download PDFInfo
- Publication number
- KR910018368A KR910018368A KR1019910006681A KR910006681A KR910018368A KR 910018368 A KR910018368 A KR 910018368A KR 1019910006681 A KR1019910006681 A KR 1019910006681A KR 910006681 A KR910006681 A KR 910006681A KR 910018368 A KR910018368 A KR 910018368A
- Authority
- KR
- South Korea
- Prior art keywords
- methyl
- salt
- formula
- compound
- sulfur
- Prior art date
Links
- 150000001732 carboxylic acid derivatives Chemical class 0.000 title claims 3
- 150000003839 salts Chemical class 0.000 claims 15
- 150000001875 compounds Chemical class 0.000 claims 10
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 10
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 9
- 229910052717 sulfur Inorganic materials 0.000 claims 9
- 239000011593 sulfur Substances 0.000 claims 9
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 8
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims 8
- 229910052760 oxygen Inorganic materials 0.000 claims 8
- 239000001301 oxygen Substances 0.000 claims 8
- 239000012453 solvate Substances 0.000 claims 3
- 150000001412 amines Chemical class 0.000 claims 2
- 239000003085 diluting agent Substances 0.000 claims 2
- 239000003814 drug Substances 0.000 claims 2
- 239000003937 drug carrier Substances 0.000 claims 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
- 239000003485 histamine H2 receptor antagonist Substances 0.000 claims 2
- 229910052739 hydrogen Inorganic materials 0.000 claims 2
- 239000001257 hydrogen Substances 0.000 claims 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 2
- DXASQZJWWGZNSF-UHFFFAOYSA-N n,n-dimethylmethanamine;sulfur trioxide Chemical group CN(C)C.O=S(=O)=O DXASQZJWWGZNSF-UHFFFAOYSA-N 0.000 claims 2
- 239000008194 pharmaceutical composition Substances 0.000 claims 2
- 239000002904 solvent Substances 0.000 claims 2
- 125000000446 sulfanediyl group Chemical group *S* 0.000 claims 2
- 229940124597 therapeutic agent Drugs 0.000 claims 2
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 claims 1
- MAROFABTHUXYCY-UHFFFAOYSA-K [Bi+3].OC(CC(=O)[O-])(CC(=O)[O-])C(=O)[O-].C(C)C(=C(N)NC)[N+](=O)[O-] Chemical compound [Bi+3].OC(CC(=O)[O-])(CC(=O)[O-])C(=O)[O-].C(C)C(=C(N)NC)[N+](=O)[O-] MAROFABTHUXYCY-UHFFFAOYSA-K 0.000 claims 1
- -1 alkyl citric acid Chemical compound 0.000 claims 1
- 229910052797 bismuth Inorganic materials 0.000 claims 1
- FKLIMYDZIBLWAA-UHFFFAOYSA-K bismuth 1-N'-[3-[[5-[(dimethylamino)methyl]furan-2-yl]methoxy]propyl]-1-N-methyl-2-nitroethene-1,1-diamine 2-hydroxypropane-1,2,3-tricarboxylate Chemical compound [Bi+3].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O.[O-][N+](=O)C=C(NC)NCCCOCC1=CC=C(CN(C)C)O1 FKLIMYDZIBLWAA-UHFFFAOYSA-K 0.000 claims 1
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 claims 1
- LUOYFQVUYMMTRC-UHFFFAOYSA-N bismuth(3+) Chemical compound [Bi+3].[Bi+3] LUOYFQVUYMMTRC-UHFFFAOYSA-N 0.000 claims 1
- 239000012458 free base Substances 0.000 claims 1
- 150000002431 hydrogen Chemical class 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 150000007530 organic bases Chemical class 0.000 claims 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 1
- 239000011975 tartaric acid Substances 0.000 claims 1
- 235000002906 tartaric acid Nutrition 0.000 claims 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D307/38—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D307/38—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D307/52—Radicals substituted by nitrogen atoms not forming part of a nitro radical
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Furan Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (17)
- 하기 일반식(Ⅰ)의 염기성 히스타민 H2-수용체 길항제와 타르타르산, 시트르산 및 알킬 시트르산 중에서 선택된 카르복실산과 비스무트의 착물이 형성하는 염 또는 이러한 염의 용매화물.상기 식 중, R1는 하기 식의 기〔식 중, R3는 메틸 또는 (CH2)2CONR4R5임 (여기서 R4및 R5는 모두 에틸기임)〕이고, R2는 수소 원자이거나 또는 R1이 -C(=CHNO2)NHCH3일 때 R2는 메틸기일 수 있고, n은 3이고 X는 산소 이거나, 또는 n이 2이고 X가 CH2또는 황이되, 단 (ⅰ) R1이 하기 식X는 황이고 n은 2이며 (ⅱ) R1이 -C(=CHNO2)NHCH3이고, R2가 수소 일 때, X는 산소이고, n은 3이거나 또는X가 CH2이고 n이 2이고, (ⅲ) R1이 -C(=CHNO2)NHCH3이고, R2가 메틸일 때, X는 산소이고 n은 3이거나 또는 X가 황이고, n이 2이다.
- 제1항에 있어서, 카르복실산이 시트르산인 염.
- 제1항 또는 제2항에 있어서, R1이 -C(=CHNO2)NHCH3이고, X가 산소이고, n이 3인 염.
- 제3항에 있어서, R2가 수소인 염.
- 제1항 또는 제2항에 있어서, R1이 하기 식의 기인 염.(식 중 R2는 수소 원자이고, X는 황이고, n은 2임)
- 제5항에 있어서, R1이 하기 식의 기인 염.
- 제1항 또는 제2항에 있어서, R1이 -C(=CHNO2)NHCH3이고, R2가 메틸이고, X가 산소이고, n이 3이거나, 또는 R1이 -C(=CHNO2)NHCH3이고, R2가 메틸이고, X가 황이고 n이 2인 염.
- 제7항에 있어서, X가 황이고 n이 2인 염.
- N-〔3-〔〔5-〔(디메틸아미노)메틸〕-2-푸라닐〕메톡시〕프로필〕-N'-메틸-2-니트로-1,1-에텐디아민 2-히드록시-1,2,3-프로판트리카르복실레이트 비스무트(3+)착물 및 그의 용매화물.
- N-〔2-〔〔〔5-〔(디메틸아미노)메틸〕-4-메틸-2-푸라닐〕메틸〕티오〕에틸-N1-메틸-2-니트로-1,1-에텐디아민 2-히드록시-1,2,3-프로판트리카르복실레이트 비스무트(3+) 착물, 5-〔〔2-〔〔〔5-〔(디메틸아미노)메틸〕-2-푸라닐〕메틸〕티오〕에틸〕아미노〕-1-메틸-1H-1,2,4-트리아졸-3-메탄올- 2-히드록시-1,2,3-프로판트리카르복실레이트 비스무트(3+)착물, 및 이들의 용매화물.
- 제1항 내지 제10항중 어느 한 항에 따른 염과, 제약상 허용되는 적어도 1종의 담체 또는 희석제로 이루어진 제약 조성물.
- 제1항 내지 제10항중 어느 한 항에 따른 염으로 이루어진 치료제.
- 제1항에서 정의된 일반식(Ⅰ)의 염기성 히스타민 H2-수용체 길항제를 적합한 용매 중에서 적당한 비스무트-카르복실산 차가물과 함께 반응시킨 후, 형성된 염을 혼합물로 부터 분리하는 것으로 이루어진, 제1항 내지 제10항 중 어느 한 항에 따른 염의 제조 방법.
- 하기 일반식(Ⅱ)의 화합물 또는 그의 제약상 허용되는 염 또는 용매화물.(식 중, X는 산소이고, n은 3이며, R3는 메틸기이건, 또는 X는 황이고, n은 2이며, R3는 -(CH2)2CON(C2H5)2임).
- 제14항에 따른 화합물과, 제약상 허용되는 적어도 1종 이상의 담체 또는 희석제로 이루어진 제약 조성물.
- 제14항에 따른 화합물로 이루어진 치료제.
- (A) 하기 일반식(Ⅲ)의 아민을 하기 일반식(Ⅳ)의 화합물과 반응시켜, X가 산소이고 n이 3이며 R3가 메틸기인 하기 일반식(Ⅱ)의 화합물을 제조하거나 (B) 하기 일반식(Ⅴ)의 화합물을 하기 일반식(Ⅵ)의 아민과 반응시켜, X가 황이고 n이 2이며 R3가 -(CH2)2CON(C2H5)2인 하기 일반식(Ⅱ)의 화합물을 제조하고, 이와 같이 하여 얻은 일반식(Ⅱ)의 화합물이 유리 염기 형태인 경우에는 임의로 이러한 유기 염기를 염으로 전환시키는 것으로 이루어진, 하기 일반식(Ⅱ)의 화합물의 제조 방법.(식 중, X는 산소이고, n은 3이며, R3는 메틸기이거나, 또는 X는 황이고, n은 2이며, R3는 -(CH2)2CON(C2H5)2이고, L은 이탈기임).※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB909009437A GB9009437D0 (en) | 1990-04-26 | 1990-04-26 | Chemical compounds |
GB9009437.6 | 1990-04-26 |
Publications (1)
Publication Number | Publication Date |
---|---|
KR910018368A true KR910018368A (ko) | 1991-11-30 |
Family
ID=10675066
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019910006681A KR910018368A (ko) | 1990-04-26 | 1991-04-25 | 카르복실산 유도체 |
Country Status (11)
Country | Link |
---|---|
US (1) | US5229418A (ko) |
EP (1) | EP0454469A1 (ko) |
JP (1) | JPH05117259A (ko) |
KR (1) | KR910018368A (ko) |
AU (1) | AU645554B2 (ko) |
CA (1) | CA2041175A1 (ko) |
GB (1) | GB9009437D0 (ko) |
IE (1) | IE911390A1 (ko) |
NZ (1) | NZ237960A (ko) |
PT (1) | PT97487A (ko) |
ZA (1) | ZA913132B (ko) |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CH679582A5 (ko) * | 1988-07-18 | 1992-03-13 | Glaxo Group Ltd | |
BG61302B1 (bg) * | 1993-09-30 | 1997-05-30 | Нихфи Ад | n-(3-(3-(1-пиперидинилметил)фенокси)пропил)хидроксиацетамид 1,2,3-пропентрикарбоксилат бисмут /3+/комплекс и метод за получаването му |
HUP9900428A2 (hu) * | 1995-01-26 | 1999-06-28 | Nycomed Imaging A/S | Bizmutvegyületek, ezeket tartalmazó diagnosztikai kontrasztanyag, ennek alkalmazása és ezt tartalmazó gyógyászati készítmény |
GB9501560D0 (en) | 1995-01-26 | 1995-03-15 | Nycomed Imaging As | Contrast agents |
SE524337C2 (sv) * | 1998-10-16 | 2004-07-27 | Astacarotene Ab | Användning av åtminstone en typ av xantofyller för framställning av ett läkemedel för profylaktisk och/eller terapeutisk behandling av matsmältningsbesvär |
WO2002042443A2 (en) * | 2000-11-23 | 2002-05-30 | MAX-PLANCK-Gesellschaft zur Förderung der Wissenschaften e.V. | Use of modulators of eukaryotic signal transduction pathways for the treatment of helicobacter infections |
JP5264494B2 (ja) | 2005-11-01 | 2013-08-14 | マウント シナイ スクール オブ メディスン | ガリウム化合物を使用する口および表在性の微生物の成長制御 |
PT2141996E (pt) * | 2007-04-02 | 2013-03-07 | Sinai School Medicine | Métodos para prevenir ou tratar doenças infecciosas utilizando compostos de gálio |
EP4196793A1 (en) | 2020-08-11 | 2023-06-21 | Université de Strasbourg | H2 blockers targeting liver macrophages for the prevention and treatment of liver disease and cancer |
Family Cites Families (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1565966A (en) * | 1976-08-04 | 1980-04-23 | Allen & Hanburys Ltd | Aminoalkyl furan derivatives |
GB2006771B (en) * | 1977-10-11 | 1982-10-20 | Glaxo Group Ltd | Substituted heterocyclic compounds their preparation and pharmaceutical compositions containing them |
US4233302A (en) * | 1977-12-23 | 1980-11-11 | Glaxo Group Limited | Amine derivatives and pharmaceutical compositions containing them |
AR228941A1 (es) * | 1978-04-26 | 1983-05-13 | Glaxo Group Ltd | Procedimiento para preparar nuevos derivados de 3,5-diamino-1,2,4-triazol que son activos contra receptores histaminicos |
DE3067920D1 (en) * | 1979-03-02 | 1984-06-28 | Glaxo Group Ltd | 1,2,4-triazole derivatives, processes for their production and pharmaceutical compositions containing them |
CA1181084A (en) * | 1980-01-08 | 1985-01-15 | Glaxo Group Limited | Process for the preparation of a furan derivative |
IT1190793B (it) * | 1982-04-27 | 1988-02-24 | Magis Farmaceutici | Composti attivi nel trattamento dell'ulcera e sintomi allergici della pelle |
HU198196B (en) * | 1984-05-02 | 1989-08-28 | Gyogyszerkutato Intezet | Process for production of basic tioether and its salts |
JPH0725745B2 (ja) * | 1986-11-11 | 1995-03-22 | 株式会社日本触媒 | アミン化合物の製造方法 |
ATE81011T1 (de) * | 1987-03-09 | 1992-10-15 | Procter & Gamble | Zusammensetzungen und ihre verwendung zur behandlung von magen-darmstoerungen. |
EP0285681B1 (de) * | 1987-04-06 | 1993-03-10 | HEUMANN PHARMA GMBH & CO | Verfahren zur Herstellung von Nitroethenderivaten |
CH679582A5 (ko) * | 1988-07-18 | 1992-03-13 | Glaxo Group Ltd | |
AU641903B2 (en) * | 1988-10-26 | 1993-10-07 | Glaxo Group Limited | Carboxylic acid derivatives |
JPH0730064B2 (ja) * | 1989-08-17 | 1995-04-05 | 協和醗酵工業株式会社 | フラン誘導体 |
-
1990
- 1990-04-26 GB GB909009437A patent/GB9009437D0/en active Pending
-
1991
- 1991-04-25 KR KR1019910006681A patent/KR910018368A/ko not_active Application Discontinuation
- 1991-04-25 US US07/691,399 patent/US5229418A/en not_active Expired - Fee Related
- 1991-04-25 EP EP91303766A patent/EP0454469A1/en not_active Withdrawn
- 1991-04-25 ZA ZA913132A patent/ZA913132B/xx unknown
- 1991-04-25 IE IE139091A patent/IE911390A1/en unknown
- 1991-04-25 CA CA002041175A patent/CA2041175A1/en not_active Abandoned
- 1991-04-25 JP JP3122426A patent/JPH05117259A/ja active Pending
- 1991-04-26 PT PT97487A patent/PT97487A/pt not_active Application Discontinuation
- 1991-04-26 NZ NZ237960A patent/NZ237960A/en unknown
- 1991-04-26 AU AU75926/91A patent/AU645554B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
NZ237960A (en) | 1993-06-25 |
ZA913132B (en) | 1992-06-24 |
US5229418A (en) | 1993-07-20 |
GB9009437D0 (en) | 1990-06-20 |
AU7592691A (en) | 1991-11-07 |
IE911390A1 (en) | 1991-11-06 |
PT97487A (pt) | 1992-01-31 |
JPH05117259A (ja) | 1993-05-14 |
EP0454469A1 (en) | 1991-10-30 |
CA2041175A1 (en) | 1991-10-27 |
AU645554B2 (en) | 1994-01-20 |
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