Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
  • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
  • C07D471/04—Ortho-condensed systems
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
  • C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
  • C07D211/80—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
  • C07D211/84—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen directly attached to ring carbon atoms
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
  • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
  • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
  • C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
  • C07D213/26—Radicals substituted by halogen atoms or nitro radicals
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
  • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
  • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
  • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen 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
  • C07D213/61—Halogen atoms or nitro radicals

Definitions

• the present invention relates first of all to an advantageous process for the preparation of the naphthyridine compounds characterized by formulas (Ia) to (Ic) below and to new intermediates which are key compounds for this process.
• Naphthyridine compounds of the formulas (Ia) to (Ic) are valuable intermediates for the preparation of active compounds, in particular highly effective bactericides (see, for example, US Pat. No. 5,164,402, US Pat. No. 5,298,629 and EP-OS 413 455).
• naphthyridine compounds of the formula (Ia) by reacting a halogenated nicotinoyl chloride with a malonic ester, then decarboxylating one of the two carboxylate groups, then converting the methylene group between the two carbonyl groups into an using an ortho-ester
• R represents hydrogen or C r C 4 alkyl
• n 1, 2 or 3, found
• R 1 represents C r C 4 alkyl
• R and R independently of one another represent C j -C 6 alkyl, where the alkyl chain can in each case optionally be interrupted by O, S or NH,
• R ', R 1 and R 2 have the meaning given for formula (III),
• Ar has the meaning given in the formulas (la) to (Ic)
• Ar, n and shark are those given in formulas (la) to (Ic),
• R and to the extent that R is C 1 -C 4 -alkyl can each be straight-chain or branched and can be, for example, methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl or t-butyl.
• R preferably represents hydrogen, methyl or ethyl.
• R preferably represents methyl or ethyl.
• the substituents can be, for example
• Ar is preferably phenyl, 2,4-difluorophenyl, 2-fluorophenyl or 4-fluorophenyl.
• Shark is preferably fluorine or chlorine. When there are two sharks, one is preferably fluorine and the other is chlorine. When there are three sharks, 1 to 2 are preferably fluorine and the rest are chlorine. It is further preferred that a fluorine substituent is located on the carbon atom in the meta position to the carbonyl group (this is the 6 position in formula (Ia) and the corresponding position in the other formulas).
• Hai ' is preferably chlorine, n is preferably 2.
• R 1 and R 2 are preferably the same and each represent methyl or ethyl, in particular ethyl.
• the reaction of compounds of the formulas (Ha) to (IIc) with a compound of the formula (III) can be carried out, for example, by initially introducing the compound of the formula (III), a solvent and a base and a compound of the formulas (Ha ) to (IIc).
• the reactants can be used in any ratio to one another.
• the molar ratio of the compound of the formulas (Ha) to (IIc) to the compound of the formula (III) is preferably 0.8 to 1.2: 1, in particular 0.9 to 1.1: 1.
• inorganic and organic bases can be used as bases.
• bases which are sparingly soluble in the reaction mixture for example inorganic bases
• a phase transfer catalyst for example inorganic bases
• Organic bases for example amines
• Tertiary amines which contain, for example, three identical or different C 1 -C 6 -alkyl groups such as triethylamine are particularly preferred.
• the amount of base should be at least the stoichiometrically required amount, a small excess is preferred, for example up to 120% by weight of the stoichiometrically required amount.
• chlorinated hydrocarbons and aromatics are suitable as solvents.
• reaction temperature can be, for example, in the range from -10 to + 80 ° C. In general, it is advantageous to stir at the reaction temperature for a while after the reactants have been combined.
• the overall process for the preparation of naphthyridine compounds of the formulas (Ic) to Ic) can be carried out in the reactor in which the fully reacted reaction mixture of reacting a compound of the formulas (Ila) to (IIc) with a compound of the formula (III) is present. Isolation of the compound of the formulas (IVa) to (IVc) produced is not necessary for this.
• reaction of a compound of the formulas (IVa) to (IVc) with a compound of the formula (V) to a compound of the formulas (Via) to (VIc) can be carried out e.g. carry out such that a compound of the formulas (IVa) to (IVc), preferably in the form of the fully reacted reaction mixture obtained in its preparation, is acidified and at temperatures of, for example, below
• (V) preferably 0.8 to 1.2: 1, in particular 0.9 to 1.1: 1.
• inorganic and organic acids can be used for acidification.
• the amount of acid can be chosen, for example, so that there is a slight excess with respect to the base used. The amount of acid can thus be, for example, up to 125 equivalent%, based on the base used.
• the laundry can e.g. at temperatures from room temperature to 95 ° C.
• the dipolar aprotic solvent can be, for example, dimethylformamide, dimethyl sulfoxide, tetramethylene sulfone or N-methylpyrrolidone.
• Suitable acid scavengers are alkali metal salts such as alkali metal fluorides, carbonates, bicarbonates and hydrides. The following may be mentioned as individual examples: sodium fluoride, sodium hydride, sodium carbonate, sodium bicarbonate, potassium fluoride and potassium bicarbonate. It is advantageous to use the acid scavenger in an excess, for example in an excess of 10 to 50% by weight, based on the theoretical required amount. It is also advantageous to carry out the cyclization under as anhydrous conditions as possible.
• an aqueous acid can be added until a pH e.g. in the
• naphthyridine compounds of the formulas (la) to (Ic) in purities of over 99%, often over 99.8%, and in yields (based on halogenated acid chloride of the formulas (I ⁇ a) to (IIc)) of over 80% d. Th. Received.
• the process according to the invention is advantageous not only because of these good results in terms of yield and purity, but also because it is particularly simple, requires only two reaction vessels and delivers highly pure products without the isolation of intermediate stages. In view of the prior art described at the outset, this is extremely surprising.
• n 1, 2 or 3
• Ar represents optionally substituted phenyl.
• Example 2 The procedure was first as in Example 2. The washed toluene solution obtained there was metered in over 3 hours onto a template heated to 60 ° C. from 250 ml of N-methylpyrrolidone and 28 g of anhydrous potassium carbonate. At the same time, toluene was continuously distilled off in vacuo.

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• Organic Chemistry (AREA)
• Nitrogen Condensed Heterocyclic Rings (AREA)

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• 1997
  • 1997-10-17 CN CN97199280A patent/CN1235605A/zh active Pending
  • 1997-10-17 CA CA002269984A patent/CA2269984A1/en not_active Abandoned
  • 1997-10-17 KR KR1019990703756A patent/KR20000052892A/ko not_active Application Discontinuation
  • 1997-10-17 JP JP10519989A patent/JP2001502715A/ja active Pending
  • 1997-10-17 AU AU50508/98A patent/AU5050898A/en not_active Abandoned
  • 1997-10-17 CZ CZ991549A patent/CZ154999A3/cs unknown
  • 1997-10-17 EP EP97913157A patent/EP0935600A1/de not_active Withdrawn
  • 1997-10-17 WO PCT/EP1997/005743 patent/WO1998018795A1/de not_active Application Discontinuation
  • 1997-10-17 PL PL97332941A patent/PL332941A1/xx unknown
  • 1997-10-17 IL IL12959797A patent/IL129597A0/xx unknown

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