JPS5645473A - Preparation of 6-fluoro-1,8-naphthyridine derivative - Google Patents
Preparation of 6-fluoro-1,8-naphthyridine derivativeInfo
- Publication number
- JPS5645473A JPS5645473A JP12222079A JP12222079A JPS5645473A JP S5645473 A JPS5645473 A JP S5645473A JP 12222079 A JP12222079 A JP 12222079A JP 12222079 A JP12222079 A JP 12222079A JP S5645473 A JPS5645473 A JP S5645473A
- Authority
- JP
- Japan
- Prior art keywords
- compound
- formula
- fluoro
- alkyl
- infection
- Prior art date
- Legal status (The legal status 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 status listed.)
- Pending
Links
- QILHGSSOWXKYFZ-UHFFFAOYSA-N 3-fluoro-1,8-naphthyridine Chemical class N1=CC=CC2=CC(F)=CN=C21 QILHGSSOWXKYFZ-UHFFFAOYSA-N 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 208000015181 infectious disease Diseases 0.000 abstract 2
- NDVLTYZPCACLMA-UHFFFAOYSA-N silver oxide Chemical compound [O-2].[Ag+].[Ag+] NDVLTYZPCACLMA-UHFFFAOYSA-N 0.000 abstract 2
- 239000003513 alkali Substances 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 239000004599 antimicrobial Substances 0.000 abstract 1
- 230000001174 ascending effect Effects 0.000 abstract 1
- IDYZIJYBMGIQMJ-UHFFFAOYSA-N enoxacin Chemical compound N1=C2N(CC)C=C(C(O)=O)C(=O)C2=CC(F)=C1N1CCNCC1 IDYZIJYBMGIQMJ-UHFFFAOYSA-N 0.000 abstract 1
- 230000001976 improved effect Effects 0.000 abstract 1
- ZFTKWAVDJBKFCS-UHFFFAOYSA-N iodine;pyridine Chemical compound [I].C1=CC=NC=C1 ZFTKWAVDJBKFCS-UHFFFAOYSA-N 0.000 abstract 1
- 231100000053 low toxicity Toxicity 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 125000006239 protecting group Chemical group 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 229910001923 silver oxide Inorganic materials 0.000 abstract 1
- 230000009885 systemic effect Effects 0.000 abstract 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 abstract 1
- 208000019206 urinary tract infection Diseases 0.000 abstract 1
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Abstract
NEW MATERIAL:A compound of formula I (R1 is H or protecting group; R2 is alkenyl, alkyl, etc.), and a salt thereof.
EXAMPLE: 1-Ethyl-6-fluoro-1,4-dihydro-4-oxo-7-( 1-piperazinyl )-1,8-naphthyridine- 3-carboxylic acid.
USE: An antimicrobial agent and a synthetic intermediate therefor having improved effects on urinary tract infection, ascending renal infection and systemic infection even in a small dose with very low toxicity.
PROCESS: A compound of formula II (R3 is H or alkyl) is oxidized with a hypohalogenate or silver oxide, or reacted with an iodine-pyridine mixture and then treated with an alkali to give the compound of formula I.
COPYRIGHT: (C)1981,JPO&Japio
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP12222079A JPS5645473A (en) | 1979-09-21 | 1979-09-21 | Preparation of 6-fluoro-1,8-naphthyridine derivative |
FI802965A FI67381C (en) | 1979-09-21 | 1980-09-19 | FRUIT PROCEDURE FOR FRAMSTAELLNING AV ETT 6-FLUORO-1,8-NAPHTHYRIDINDERIVAT ANVAENDBART SOM ANTIBAKTERIELLT MEDEL |
ES495190A ES8106902A1 (en) | 1979-09-21 | 1980-09-19 | Preparation of 66fluoroo1*88naphthyridine derivative |
HU802307A HU184827B (en) | 1979-09-21 | 1980-09-19 | Process for preparing 6-fluoro-1,8-na phthy ridyl-derivatives |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP12222079A JPS5645473A (en) | 1979-09-21 | 1979-09-21 | Preparation of 6-fluoro-1,8-naphthyridine derivative |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS5645473A true JPS5645473A (en) | 1981-04-25 |
Family
ID=14830515
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP12222079A Pending JPS5645473A (en) | 1979-09-21 | 1979-09-21 | Preparation of 6-fluoro-1,8-naphthyridine derivative |
Country Status (4)
Country | Link |
---|---|
JP (1) | JPS5645473A (en) |
ES (1) | ES8106902A1 (en) |
FI (1) | FI67381C (en) |
HU (1) | HU184827B (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1993025545A1 (en) * | 1992-06-09 | 1993-12-23 | Korea Research Institute Of Chemical Technology | Novel quinoline derivatives and processes for preparing the same |
-
1979
- 1979-09-21 JP JP12222079A patent/JPS5645473A/en active Pending
-
1980
- 1980-09-19 HU HU802307A patent/HU184827B/en unknown
- 1980-09-19 ES ES495190A patent/ES8106902A1/en not_active Expired
- 1980-09-19 FI FI802965A patent/FI67381C/en not_active IP Right Cessation
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1993025545A1 (en) * | 1992-06-09 | 1993-12-23 | Korea Research Institute Of Chemical Technology | Novel quinoline derivatives and processes for preparing the same |
Also Published As
Publication number | Publication date |
---|---|
FI802965A (en) | 1981-03-22 |
ES495190A0 (en) | 1981-09-01 |
FI67381C (en) | 1985-03-11 |
ES8106902A1 (en) | 1981-09-01 |
HU184827B (en) | 1984-10-29 |
FI67381B (en) | 1984-11-30 |
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