RU93004405A - Derivatives of quinolone and naftyridoncarbonic acid in the form of a mixture of isomers or individual isomers, their hydrates and salt, method of their production and containing their medicinal product - Google Patents
Derivatives of quinolone and naftyridoncarbonic acid in the form of a mixture of isomers or individual isomers, their hydrates and salt, method of their production and containing their medicinal productInfo
- Publication number
- RU93004405A RU93004405A RU93004405/33A RU93004405A RU93004405A RU 93004405 A RU93004405 A RU 93004405A RU 93004405/33 A RU93004405/33 A RU 93004405/33A RU 93004405 A RU93004405 A RU 93004405A RU 93004405 A RU93004405 A RU 93004405A
- Authority
- RU
- Russia
- Prior art keywords
- isomers
- alkyl
- quinolone
- hydrates
- derivatives
- Prior art date
Links
- 150000004677 hydrates Chemical class 0.000 title claims 2
- 238000004519 manufacturing process Methods 0.000 title claims 2
- 239000000203 mixture Substances 0.000 title claims 2
- 150000007660 quinolones Chemical class 0.000 title claims 2
- 150000003839 salts Chemical class 0.000 title claims 2
- 239000011780 sodium chloride Substances 0.000 title claims 2
- 239000002253 acid Substances 0.000 title 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 4
- 239000001257 hydrogen Substances 0.000 claims 4
- 150000002431 hydrogen Chemical class 0.000 claims 3
- -1 5-methyl-2-oxo-1,3-dioxol-4-yl-methyl Chemical group 0.000 claims 2
- 229910052736 halogen Inorganic materials 0.000 claims 2
- 150000002367 halogens Chemical class 0.000 claims 2
- SNLMOXFUCILIPL-UHFFFAOYSA-N 1,8-naphthyridine-2-carboxylic acid Chemical compound C1=CC=NC2=NC(C(=O)O)=CC=C21 SNLMOXFUCILIPL-UHFFFAOYSA-N 0.000 claims 1
- 125000003277 amino group Chemical group 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 1
- 239000003814 drug Substances 0.000 claims 1
- 229940079593 drugs Drugs 0.000 claims 1
- 125000005843 halogen group Chemical group 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- 0 C[C@]1C2NCC*C2CN(C)C1 Chemical compound C[C@]1C2NCC*C2CN(C)C1 0.000 description 1
Claims (1)
где A - CH, CF, CCL, C-OCH3, C-CH3, N; X1 - водород, галоген, NH2, CH3; R1 - C1 - C3-алкил, FCH2CH2-, циклопропил, фенил, который может быть от одного до трех раз замещен галогеном, или A и R1 вместе мостик структуры C-O-CH2-CH(CH)3; R2 - водород, C1 - C3-алкил, который может быть замещен гидроксигруппой, галогеном или аминогруппой, или 5-метил-2-оксо-1,3-диоксол-4-ил-метил, B - остаток формул
где Y - О или CH2; R3 - оксо-C2 - C5-алкил, CH2-CO-C6H5, CH2CH2CO2R', R'O2C-CH= C-CO2R', -CH= CH-CO2R' или CH2CH2-CH, где R' - водород или C1 - C3-алкил; R4 - водород, C1 - C3-алкил, оксо-C2 - C5-алкил, CH2-CO-C6H5, CH2CH2CO2R', R'O2C-CH= CO2R', -CH=CH-CO2-R или CH2CH2-CN или 5-метил-2-оксо-1,3-диоксол-4-ил-метил, где R' имеет указанное значение, в виде смеси изомеров или отдельных изомеров, их гидраты и соли. Другими объектами изобретения являются способ получения соединений формулы I и содержащее их лекарственное средство.The object of the invention are derivatives of quinolone and naphthyridinecarboxylic acid of General formula
where A is CH, CF, CCL, C-OCH 3 , C-CH 3 , N; X 1 is hydrogen, halogen, NH 2 , CH 3 ; R 1 - C 1 - C 3 -alkyl, FCH 2 CH 2 -, cyclopropyl, phenyl, which can be substituted one to three times with halogen, or A and R 1 together bridge the structure CO — CH 2 -CH (CH) 3 ; R 2 is hydrogen, C 1 - C 3 -alkyl, which may be substituted by a hydroxy group, halogen or amino group, or 5-methyl-2-oxo-1,3-dioxol-4-yl-methyl, B is the residue of the formulas
where Y is O or CH 2 ; R 3 - oxo-C 2 - C 5 -alkyl, CH 2 -CO-C 6 H 5 , CH 2 CH 2 CO 2 R ', R'O 2 C-CH = C-CO 2 R', -CH = CH — CO 2 R ′ or CH 2 CH 2 —CH, where R ′ is hydrogen or C 1 –C 3 -alkyl; R 4 is hydrogen, C 1 - C 3 -alkyl, oxo-C 2 - C 5 -alkyl, CH 2 -CO-C 6 H 5 , CH 2 CH 2 CO 2 R ', R'O 2 C-CH = CO 2 R ', -CH = CH-CO 2 -R or CH 2 CH 2 -CN or 5-methyl-2-oxo-1,3-dioxol-4-yl-methyl, where R' has the indicated value, in as a mixture of isomers or individual isomers, their hydrates and salts. Other objects of the invention are a method for producing compounds of the formula I and a drug containing them.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE4200414A DE4200414A1 (en) | 1992-01-10 | 1992-01-10 | New quinoline and naphthyridinone-carboxylic acid derivs. |
| DEP4200414.4 | 1992-01-10 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| RU93004405A true RU93004405A (en) | 1995-06-19 |
| RU2105770C1 RU2105770C1 (en) | 1998-02-27 |
Family
ID=6449288
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU93004405/04A RU2105770C1 (en) | 1992-01-10 | 1993-01-11 | Quinolone-and naphthiridonecarboxylic acid derivatives in admixture with isomers or individual isomers, hydrates and salts thereof, and pharmaceutical composition |
Country Status (5)
| Country | Link |
|---|---|
| DE (1) | DE4200414A1 (en) |
| PL (1) | PL175558B1 (en) |
| RU (1) | RU2105770C1 (en) |
| UA (1) | UA35554C2 (en) |
| ZA (1) | ZA93125B (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PL2364141T5 (en) | 2008-12-08 | 2018-02-28 | Ratiopharm Gmbh | Compacted moxifloxacin |
| EP2429991B1 (en) | 2009-05-15 | 2014-09-10 | Redx Pharma Limited | Redox drug derivatives |
| UA106556C2 (en) | 2013-05-13 | 2014-09-10 | Наталья Николаевна Деркач | Method of obtaining (1-cyclopropyl -6- fluoro-1,4-dihydro methoxy -8 -7 - [(4as, 7as) - oktahydro -6n- pyrrolo [3,4-pyridine bsch - 6- yl] -4-oxo-3-hinolinkarbonovoyi acid |
-
1992
- 1992-01-10 DE DE4200414A patent/DE4200414A1/en not_active Withdrawn
-
1993
- 1993-01-08 PL PL93320107A patent/PL175558B1/en unknown
- 1993-01-08 ZA ZA93125A patent/ZA93125B/en unknown
- 1993-01-11 RU RU93004405/04A patent/RU2105770C1/en active
- 1993-04-16 UA UA93002762A patent/UA35554C2/en unknown
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