JPS5569582A - 1,7-phenanthroline-3-carboxylic acid derivative - Google Patents

1,7-phenanthroline-3-carboxylic acid derivative

Info

Publication number
JPS5569582A
JPS5569582A JP14178678A JP14178678A JPS5569582A JP S5569582 A JPS5569582 A JP S5569582A JP 14178678 A JP14178678 A JP 14178678A JP 14178678 A JP14178678 A JP 14178678A JP S5569582 A JPS5569582 A JP S5569582A
Authority
JP
Japan
Prior art keywords
formula
compound
solvent
alkyl group
lower alkyl
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.)
Granted
Application number
JP14178678A
Other languages
Japanese (ja)
Other versions
JPS5854151B2 (en
Inventor
Hiroshi Ishikawa
Fujio Tafusa
Kazuyuki Nakagawa
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Otsuka Pharmaceutical Co Ltd
Original Assignee
Otsuka Pharmaceutical Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Otsuka Pharmaceutical Co Ltd filed Critical Otsuka Pharmaceutical Co Ltd
Priority to JP53141786A priority Critical patent/JPS5854151B2/en
Publication of JPS5569582A publication Critical patent/JPS5569582A/en
Publication of JPS5854151B2 publication Critical patent/JPS5854151B2/en
Expired legal-status Critical Current

Links

Landscapes

  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

NEW MATERIAL:A compound of formula 1a: (R1 is H or lower alkyl group; R4 is lower alkyl group) or formula 1b, and its salt.
EXAMPLE: 9, 10-Dihydro-4, 8-dioxo-1H, 4H, 7H-1, 7-phenanthroline-3-carboxylic acid.
USE: Antibacterials effective against Gram-positive and Gram-negative bacteria, carcinostatics, and antiviral agents, having low toxicity.
PROCESS: A carbostyril derivative of formula 2 is reacted with a malonic acid derivative of formula 3: (R3 is lower alkyl group) in the presence or absence of a solvent, e.g. methanol, at room temperature to 150°C to give a compound of formula 4, which is then subjected to ring closure in a solvent, e.g. diphenyl ether, at 100W 250°C to form the compound of formula 1a. The resulting compound is then hydrolyzed in a solvent, e.g. methanol, in the presence of a catalyst, e.g. NaOH, at room temperature to 200°C to afford the compound of formula 1b.
COPYRIGHT: (C)1980,JPO&Japio
JP53141786A 1978-11-16 1978-11-16 1,7↓-phenanthroline↓-3↓-carboxylic acid derivative Expired JPS5854151B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP53141786A JPS5854151B2 (en) 1978-11-16 1978-11-16 1,7↓-phenanthroline↓-3↓-carboxylic acid derivative

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP53141786A JPS5854151B2 (en) 1978-11-16 1978-11-16 1,7↓-phenanthroline↓-3↓-carboxylic acid derivative

Publications (2)

Publication Number Publication Date
JPS5569582A true JPS5569582A (en) 1980-05-26
JPS5854151B2 JPS5854151B2 (en) 1983-12-02

Family

ID=15300122

Family Applications (1)

Application Number Title Priority Date Filing Date
JP53141786A Expired JPS5854151B2 (en) 1978-11-16 1978-11-16 1,7↓-phenanthroline↓-3↓-carboxylic acid derivative

Country Status (1)

Country Link
JP (1) JPS5854151B2 (en)

Also Published As

Publication number Publication date
JPS5854151B2 (en) 1983-12-02

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