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US4804760A Expired / Lapsed US ⏱️ 0.0 years remaining

Process for the preparation of 4-hydroxy-quinoline-3-carboxylic acids

Assignee: Bayer AG
•
Filing: 1987-04-28
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Granted: 1989-02-14
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Expires: 2007-04-28
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Abstract

Abstract A process for the preparation of a compound of the formula ##STR1## in which Y is a nitrile group, an ester group COOR 1 or an acid amide CONR 2 R 3 , R 1 , R 2 and R 3 each independently is hydrogen or C 1 -C 4 -alkyl, and R 3 may also be phenyl, and X 2 , X 3 , X 4 and X 5 each independently is hydrogen, halogen, nitro, cyano, alkyl having 1-3 carbon atoms, alkoxy having 1-3 carbon atoms, alkylmercapto having 1-3 carbon atoms, alkyl-sulphonyl having 1-3 carbon atoms, or a phenylsulphonyl group which is optionally substituted in the aryl radical, comprising reacting an aminoacrylate of the formula in which X 1 is halogen, a nitro group, an alkoxy, alkoxy, alkylmercapto or alkylsulphonyl group having 1-3 carbon atoms in each case, or an arylsulphonyl group, W is hydrogen or a --CH 2 CH 2 Z radical, Z is a nitrile group, an ester group COOR 4 or an acid amide group CONR 5 R 6 , and R 4 , R 5 and R 6 each independently is hydrogen or C 1 -C 4 -alkyl, and R 5 may also be phenyl, with an acid acceptor in an aprotic solvent. Some of the reactants are new, as are the products which are intermediates for antibacterially active 1-alkyl-4-quinolone-3-carboxylic acids.

Inventors

  • 👤 Michael Schriewer
  • 👤 Klaus Grohe

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-07 11:38
CPC Classifications
C; C07; C07D; C07D215/00; C07D215/02; C07D215/16; C07D215/48; C07D215/54; C07D215/56; C07C; C07C205/00; C07C205/49; C07C205/56; C07C205/57; C07C205/58; C07C205/61; C07C45/00; C07C45/45; C07C45/46; C07C49/00; C07C49/76; C07C49/80; C07C49/807

Claims Analysis

Total Claims: 4
Claim 1
Independent Claim 214 words
A process for the preparation of a compound of the formula ##STR26## in which Y is a nitrile group, an ester group COOR 1 or an acid amide CONR 2 R 3 , R 1 , R 2 and R 3 each independently is hydrogen or C 1 -C 4 -alkyl, and R 3 may also be phenyl, and X 2 , X 3 , X 4 and X 5 each independently is hydrogen, halogen, nitro, cyano, alkyl having 1--4 carbon atoms, alkoxy having 1-3 carbon atoms, alkylmercapto having 1-3 carbon atoms, alkylsulphonyl having 1-3 carbon atoms, or a phenylsulphonyl group which is optionally substituted in the aryl radical, comprising reacting an aminoacrylate of the formula ##STR27## in which X 1 is halogen, Z is a nitrile group, an ester group COOR 4 or an acid amide group CONR 5 R 6 , and R 4 , R 5 and R 6 each independently is hydrogen or C 1 -C 4 -alkyl, and R 5 may also be phenyl, with an acid acceptor selected from the group consisting of potassium tert.-butanolate, 1,4-diazabicyclo[2,2,2]-octane (DABCO), 1,8-diazo-bicyclo[5,4,0]undec-7-ene (DBU), butyl-lithium, phenyl-lithium, phenyl-magnesium bromide, sodium methylate, sodium ethylate, sodium hydroxide, sodium carbonate and potassium carbonate, in an aprotic solvent in the presence of about one equivalent of a base.
Claim 2
Dependent Claim 214 words
A process for the preparation of a compound of the formula ##STR26## in which Y is a nitrile group, an ester group COOR 1 or an acid amide CONR 2 R 3 , R 1 , R 2 and R 3 each independently is hydrogen or C 1 -C 4 -alkyl, and R 3 may also be phenyl, and X 2 , X 3 , X 4 and X 5 each independently is hydrogen, halogen, nitro, cyano, alkyl having 1--4 carbon atoms, alkoxy having 1-3 carbon atoms, alkylmercapto having 1-3 carbon atoms, alkylsulphonyl having 1-3 carbon atoms, or a phenylsulphonyl group which is optionally substituted in the aryl radical, comprising reacting an aminoacrylate of the formula ##STR27## in which X 1 is halogen, Z is a nitrile group, an ester group COOR 4 or an acid amide group CONR 5 R 6 , and R 4 , R 5 and R 6 each independently is hydrogen or C 1 -C 4 -alkyl, and R 5 may also be phenyl, with an acid acceptor selected from the group consisting of potassium tert.-butanolate, 1,4-diazabicyclo[2,2,2]-octane (DABCO), 1,8-diazo-bicyclo[5,4,0]undec-7-ene (DBU), butyl-lithium, phenyl-lithium, phenyl-magnesium bromide, sodium methylate, sodium ethylate, sodium hydroxide, sodium carbonate and potassium carbonate, in an aprotic solvent in the presence of about one equivalent of a base.
Claim 3
Dependent Claim 21 words
A process according to claim 1, wherein the reaction is carried out at a temperature from about 60° to 300° C.
Claim 4
Dependent Claim 20 words
A process according to claim 1, wherein the reaction is carried out a temperature from about 80° to 180° C.

References Cited (Backward Citations)

DE2854558A1 Cited
GB2015513A Cited
US4670444A Cited
US4670444B1 Cited
EP0168733A2 Cited
EP0168737A2 Cited
US4680401A Cited
EP0176846A2 Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1992-02-14 1992-08-15 1993-02-14 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1996-02-14 1996-08-15 1997-02-14 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 2000-02-14 2000-08-15 2001-02-14 $7700.00 Window Closed / Lapsed

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