BE902586A - Composes a activite antibacterienne, leur procede de fabrication et compositions pharmaceutiques les comprenant. - Google Patents
Composes a activite antibacterienne, leur procede de fabrication et compositions pharmaceutiques les comprenant.Info
- Publication number
- BE902586A BE902586A BE0/215132A BE215132A BE902586A BE 902586 A BE902586 A BE 902586A BE 0/215132 A BE0/215132 A BE 0/215132A BE 215132 A BE215132 A BE 215132A BE 902586 A BE902586 A BE 902586A
- Authority
- BE
- Belgium
- Prior art keywords
- compounds
- group
- manufacturing
- same
- pharmaceutical compositions
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 3
- 230000000844 anti-bacterial effect Effects 0.000 title abstract 2
- 238000004519 manufacturing process Methods 0.000 title 1
- 239000008194 pharmaceutical composition Substances 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 1
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 abstract 1
- 238000010521 absorption reaction Methods 0.000 abstract 1
- 125000002252 acyl group Chemical group 0.000 abstract 1
- 125000005041 acyloxyalkyl group Chemical group 0.000 abstract 1
- 125000004183 alkoxy alkyl group Chemical group 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000005205 alkoxycarbonyloxyalkyl group Chemical group 0.000 abstract 1
- -1 aroyloxyalkyl Chemical group 0.000 abstract 1
- 125000005098 aryl alkoxy carbonyl group Chemical group 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 150000004677 hydrates Chemical class 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 150000007522 mineralic acids Chemical class 0.000 abstract 1
- 125000002950 monocyclic group Chemical group 0.000 abstract 1
- 150000007524 organic acids Chemical class 0.000 abstract 1
- 235000005985 organic acids Nutrition 0.000 abstract 1
- 125000004043 oxo group Chemical group O=* 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 238000001228 spectrum Methods 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D215/48—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
- C07D215/54—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen attached in position 3
- C07D215/56—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen attached in position 3 with oxygen atoms in position 4
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Cephalosporin Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Quinoline Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Composés répondant à la formule générale (1) : dans laquelle R représante un groupe alcoxyalkyle, alcanoyloxyalkyle, aroyloxyalkyle, alcoxycarbonyloxyalkyle, alcoxycarbonyle, aralkyloxycarbonyle, ou un groupe hétérocycle, monocyclique ou bicylique, substitué éventuellement à son tour par un groupe alkyle C1-C4 ou des groupes oxo, les groupes alkyle, alcoxy et alcanoyle cités ci-dessus pouvant etre linéaires ou ramifiés et contenant de 1 à 5 atomes de carbone; et R1 représente l'hydrogène ou un groupe alkyle inférieur, de préférence le méthyle, ainsi que leurs hydrates ou leurs sels d'addition avec des acides inorganiques ou organiques, acceptables du point de vue pharmaceutique, et les éventuels énantiomères et/ou diastéréoisomères. Ces composés présentent un spectre d'activité et antibactérienne une puissance supérieure, mais avec une faible absorption.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT8421241A IT1213173B (it) | 1984-06-04 | 1984-06-04 | Composti ad attivita'antibatterica, procedimento per laloro preparazione e relative composizioni farmaceutiche. |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE902586A true BE902586A (fr) | 1985-09-30 |
Family
ID=11178899
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE0/215132A BE902586A (fr) | 1984-06-04 | 1985-06-04 | Composes a activite antibacterienne, leur procede de fabrication et compositions pharmaceutiques les comprenant. |
Country Status (7)
| Country | Link |
|---|---|
| KR (1) | KR870000286B1 (fr) |
| BE (1) | BE902586A (fr) |
| CH (1) | CH666264A5 (fr) |
| ES (1) | ES8604193A1 (fr) |
| GB (1) | GB2160519B (fr) |
| IT (1) | IT1213173B (fr) |
| PT (1) | PT80590B (fr) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3525108A1 (de) * | 1985-06-07 | 1986-12-11 | Bayer Ag, 5090 Leverkusen | Antibakteriell wirksame chinoloncarbonsaeureester |
| DE3601566A1 (de) * | 1986-01-21 | 1987-07-23 | Bayer Ag | Pharmazeutische zubereitungen von ciprofloxacin |
| US5286754A (en) * | 1986-01-21 | 1994-02-15 | Bayer Aktiengesellschaft | Pharmaceutical formulations of ciprofloxacin |
| FR2594439B1 (fr) * | 1986-02-19 | 1989-04-21 | Vetoquinol Sa | Nouveaux derives ester, thioester et amide de quinolone, leur procede de preparation et leur application en therapeutique |
| US5262417A (en) * | 1988-12-06 | 1993-11-16 | The Upjohn Company | Antibacterial quinolone compounds |
| US5066800A (en) * | 1990-04-27 | 1991-11-19 | Hoffmann-La Roche Inc. | Qunoline intermediates useful therein for synthesizing antibacterial compounds |
| ES2050594B1 (es) * | 1991-12-31 | 1994-12-16 | Ind Quimica Agropecuaria S A | Procedimiento para la obtencion de acidos 6-fluoro-1,4-dihidro-4-oxo-7-piperazino-quinolin-3-carboxilicos sustituidos en 1-n. |
| ES2048110B1 (es) * | 1992-07-22 | 1995-02-01 | Prodesfarma Sa | Procedimiento de preparacion de 2,2-dioxidos de pirazino (2,3-c)-1,2,6-tiadiazina n(1) sustituidos. |
| EP1609818B1 (fr) * | 2004-06-24 | 2010-03-10 | Bayer MaterialScience AG | Compositions de polycarbonate stabilisées contre la chaleur |
| CN109942488A (zh) * | 2019-04-04 | 2019-06-28 | 山东省联合农药工业有限公司 | 一种喹啉羧酸酯类化合物及其制备方法与用途 |
-
1984
- 1984-06-04 IT IT8421241A patent/IT1213173B/it active
-
1985
- 1985-05-29 CH CH2265/85A patent/CH666264A5/it not_active IP Right Cessation
- 1985-06-03 GB GB08513962A patent/GB2160519B/en not_active Expired
- 1985-06-03 ES ES543820A patent/ES8604193A1/es not_active Expired
- 1985-06-04 BE BE0/215132A patent/BE902586A/fr not_active IP Right Cessation
- 1985-06-04 PT PT80590A patent/PT80590B/pt unknown
- 1985-06-04 KR KR1019850003890A patent/KR870000286B1/ko not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| PT80590B (en) | 1987-04-21 |
| IT1213173B (it) | 1989-12-14 |
| KR860000282A (ko) | 1986-01-27 |
| ES8604193A1 (es) | 1986-01-16 |
| CH666264A5 (it) | 1988-07-15 |
| ES543820A0 (es) | 1986-01-16 |
| GB8513962D0 (en) | 1985-07-03 |
| KR870000286B1 (ko) | 1987-02-25 |
| PT80590A (en) | 1985-07-01 |
| GB2160519B (en) | 1988-07-20 |
| GB2160519A (en) | 1985-12-24 |
| IT8421241A0 (it) | 1984-06-04 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| HUT51267A (en) | Process for prodicing new thiochroman esters of phenols and terephthalates and pharmaceutical compositions comprising same as active ingredient | |
| FR2372176A1 (fr) | Procede de preparation de derives d'alcoxy-3 androstanones-17 | |
| BE900345A (fr) | Composition pharmaceutique ophtalmiques a base d'un derive d'acide phenylacetique. | |
| LU91210I2 (fr) | Emodepside & Praziquantel ainsi que leurs dérivés pharmaceutiqement acceptables (PROFENDER) | |
| KR930703303A (ko) | 1, 4-벤조티아제핀 유도체 | |
| BE902586A (fr) | Composes a activite antibacterienne, leur procede de fabrication et compositions pharmaceutiques les comprenant. | |
| FR2426694A1 (fr) | Cephalosporines perfectionnees, leur procede de preparation et leur application therapeutique | |
| ES2060173T3 (es) | Derivados de lisolecitina para el tratamiento de enfermedades autoinmunologicas. | |
| KR950702831A (ko) | 심장 보호제(cardio-protective agent) | |
| NO860586L (no) | Fremgangsmaate for fremstilling av antiandrogent aktive forbindelser. | |
| CA2020923A1 (fr) | Derives d'urethanne, leur preparation et leur application notamment comme agents hydratants dans des compositions cosmetiques ou pharmaceutiques destinees au traitement des peaux seches | |
| BE901987A (fr) | Derives d'alcanolamines et inhibiteurs de l'agregation des plaquettes en contenant comme principe actif. | |
| BE904983A (fr) | Acides propenylaminothiazolylcephalosporaniques 3-substitues et leurs esters. | |
| KR890701576A (ko) | 2,5,6,7-테트라놀-4,8-인터-m-페닐렌 PGI₂유도체 및 그 제조법과 용도 | |
| BE905654A (fr) | Derives de la armstrong 2-1,2,4-triazoline-5-one, procede pour leur preparation et leurs utilisations. | |
| KR890701584A (ko) | 20, 21-디노르에비나메닌의 신규 치환 유도체, 그의 제조 방법 및 이 방법으로 얻는 신규 중간체, 약제로서의 그의 용도 및 그를 함유하는 제약 조성물 | |
| KR880011163A (ko) | 4- 벤질- 피페라지닐 하이드라존 | |
| BE901831A (fr) | Derives d'aminodiaryl sulfoxyde, procede pour leur preparation et compositions pharmaceutiques et pesticides les contenant. | |
| BE1002696A3 (fr) | Derives de dioxazocine, leur procede de preparation et compositions pharmaceutiques les contenant. | |
| BE1003280A3 (fr) | Derives oxo-isoindoliniques optiquement actifs. | |
| BE899823A (fr) | Acide 2-(4-biphenylyl)-4-hexenoique et ses derives, doues d'une activite antiinflammatoire. | |
| DE19705718A1 (de) | Neue Oxirancarbonsäuren zur Behandlung des Diabetes Typ 2 und anderer insulinresistenter Zustände | |
| FR2394527A1 (fr) | N-(3'-phenylthiopropyl)-3,3-diphenylpropylamines substituees dotees d'activite pharmacologique et compositions pharmaceutiques les contenant | |
| ES510828A0 (es) | "un procedimiento para la preparacion de un derivado de morfolina". | |
| BE905432A (fr) | Nouveaux derives du catechol, un procede pour leur preparation, et compositions therapeutiques a base de ces derives. |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| RE | Patent lapsed |
Owner name: CHIESI FARMACEUTICI S.P.A. Effective date: 19890630 |