Pyrido[1,2-a]pyrimidine derivatives

This invention relates to pyrido[1,2-a]pyrimidine derivatives, a process for the preparation thereof and pharmaceutical compositions containing the same.
The present invention is directed more particularly to 2-alkyl-3-substituted-4-oxo-4H-pyrido[1,2-a]pyrimidines. The great majority of the compounds of the present invention are new, never described in prior art.
There are, however, a few publications dealing with 2-alkyl-3-substituted-4-oxo-4H-pyrido[1,2-a]pyrimidines. It is known that 2-aminopyridine and ethyl-2-methyl-acetoacetate or ethyl-2-ethyl-acetoacetate may be reacted in a molar ratio of 1:1.5 in polyphosphoric acid at 100.degree. C.; on neutralizing the reaction mixture the corresponding pyrido[1,2-a]pyrimidines are obtained (J. Org. Chem. 33, 3015 (1968)). According to another method 2-aminopyridine and ethyl-2-methyl-acetoacetate are reacted at 165.degree. C. in the presence of polyphosphoric acid ethyl ester, the reaction mixture is poured onto ice cold water and neutralized with ammonia. After column-chromatographic purification 2,3-dimethyl-4-oxo-4H-pyrido[1,2-a]pyrimidine is obtained with a yield of 42%; mp.: 119.5.degree.-121.degree. C. (J. Chem. Soc. C. 1970, 829 and J. Chem. Soc. C. 1971, 2163). In these publications the 2,3-dimethyl-, 2-methyl-3-ethyl-, 2,3,7-trimethyl-, 2-methyl-3-ethyl-7-bromo- and 2,6,8-trimethyl-3-ethyl-4-oxo-4 H-pyrido[1,2-a]pyrimidine are described without disclosure of any therapeutical utility of these compounds.
According to a feature of the present invention there are provided new pyrido[1,2-a]pyrimidine derivatives of the formula I ##STR2## and salts and quaternary salts thereof (wherein R is hydrogen, halogen, lower alkyl, nitro, hydroxy, amino, lower alkoxy, carboxy or a derivative of the carboxy group;
R.sup.1 is hydrogen, halogen or lower alkyl;
R.sup.2 is an alkyl group having 1 to 16 carbon atoms;
R.sup.3 is an alkyl group having 1 to 16 carbon atoms, a C.sub.7-12 aralkyl group optionally halogeno-substituted in the aromatic ring: or a cycloalkyl-alkyl group having 6 to 12 carbon atoms; and
R.sup.4 is a single electron pair, a hydrogen atom or a lower alkyl group;
the dotted lines represent optional bonds;
with the proviso that if all the dotted lines are further bonds, R.sup.2 and R.sup.3 are methyl and R.sup.1 is hydrogen, then R is other than hydrogen or 7-methyl; and with the further proviso that if all the dotted lines are further bonds, R.sup.2 is methyl, R.sup.3 is ethyl and R.sup.1 is hydrogen, then R is other than hydrogen or 7-bromo and with the further proviso that if all the dotted lines are further bonds, R.sup.2 is methyl, R.sup.3 is ethyl and R.sup.1 is 6-methyl, then R is other than 8-methyl).
The term "lower alkyl" used throughout the specification identifies straight or branched chain alkyl groups having 1 to 6, preferably 1 to 4 carbon atoms (e.g. methyl, ethyl, n-propyl, isopropyl, N-butyl etc.). The term "lower alkoxy" means straight or branched chain alkoxy groups having 1 to 6, preferably 1 to 4 carbon atoms (e.g. methoxy, ethoxy, n-propoxy, isopropoxy etc.). The term "halogen" encompasses the fluorine, chlorine, bromine and iodine atoms. If R.sup.2 or R.sup.3 stand for C.sub.1-16 alkyl groups they can represent methyl, ethyl, n-propyl, isopropyl, n-butyl, n-pentyl, n-hexyl, n-decyl n-dodecyl groups etc. The term "derivative of the carboxy group" relates to esters (e.g. alkyl, aryl, preferably phenyl, or aralkyl preferably benzyl esters), acid amides (e.g. carbamoyl, N-alkyl- or N,N-dialkyl-carbamoyl groups etc.), acid azides, acid hydrazides or nitriles. The said acid derivatives can be preferably lower alkyl esters (alkoxy-carbonyl). The term "C.sub.7-12 aralkyl" may be preferably benzyl, beta-phenyl-ethyl, gamma-phenyl-propyl etc. The C.sub.6-12 cyclo alkyl-alkyl group can be preferably cyclohexyl-methyl, cyclopentyl-methyl, cyclohexyl-ethyl etc.
The salts of the compounds of the formula I can be pharmaceutically acceptable salts formed with organic or inorganic acids (e.g. hydrochlorides, hydrobromides, hydroiodides, sulfates, phosphates, maleates, tartarates, acetates, lactates, fumarates etc). The quaternary salts may be formed with conventional quaternarizing agents (e.g. with alkyl halides or dialkyl sulfates such as methoiodides, methobromides, methochlorides, methosulfates, ethoiodides etc.).
In a preferred group of the compounds of formula I, R.sup.2 is C.sub.1-6 alkyl, R.sup.3 is C.sub.1-6 alkyl; R is 6-methyl and R.sup.1 is hydrogen. Those compounds are particularly preferred when the bonds marked by a dotted line are not hydrogenated.
A particularly advantageous group consists of those compounds of the formula I in which R is hydrogen, chlorine, methyl, nitro, hydroxy, carboxy or lower alkoxycarbonyl; R.sup.1 is hydrogen or methyl; R.sup.2 is methyl, ethyl, n-propyl or isopropyl; R.sup.3 is methyl, ethyl, n-propyl, isopropyl, n-butyl, n-dodecyl, benzyl, p-chlorobenzyl or cyclohexylmethyl; R.sup.4 stands for a single electron pair, hydrogen or methyl; and the dotted lines represent optional further bonds with the provisos enumerated before.
Particularly preferred representatives of the compounds of the formula I are the following derivatives:
2,3,6-trimethyl-4-oxo-4H-pyrido[1,2-a]pyrimidine and its acid-addition salts and quaternary salts;
3,6-dimethyl-2-ethyl-4-oxo-4H-pyrido[1,2-a]pyrimidine and its acid-addition salts and quaternary salts;
2-methyl-3-n-propyl-4-oxo-4H-pyrido[1,2-a]pyrimidine and its acid-addition salts and quaternary salts;
2,6-dimethyl-3-n-propyl-4-oxo-4H-pyrido[1,2-a]pyrimidine and its acid-addition salts and quaternary salts;
2,9-dimethyl-3-ethyl-4-oxo-4H-pyrido[1,2-a]pyrimidine and its acid-addition salts and quaternary salts;
2,9-dimethyl-3-ethyl-4-oxo-4H-pyrido[1,2-a]pyrimidine and its acid-addition salts and quaternary salts;
2,7-dimethyl-3-ethyl-4-oxo-4H-pyrido[1,2-a]pyrimidine and its acid-addition salts and quaternary salts;
2,8-dimethyl-3-ethyl-4-oxo-4H-pyrido[1,2-a]pyrimidine and its acid-addition salts and quaternary salts;
2-methyl-3-ethyl-7-chloro-4-oxo-4H-pyrido[1,2-a]pyrimidine and its acid-addition salts and quaternary salts thereof; and
2,6-dimethyl-3-n-butyl-4-oxo-4H-pyrido[1,2-a]pyrimidine and its acid-addition salts and quaternary salts thereof.
A highly active compound of the formula I is the 2,6-dimethyl-3-ethyl-4-oxo-4H-pyrido[1,2-a]pyrimidine and salts and quaternary salts--especially the hydrochloride--thereof.
It is known that 1,6-dimethyl-3-ethoxycarbonyl-4-oxo-4H-6,7,8,9-tetrahydro-pyrido[1,2-a]pyrimidinium-methosulfate (referred to below as Probon, British Pat. No. 1,209,946) is an outstanding analgesic of the pyrido[1,2-a]pyrimidine group. The analgesic effect is only one of the manifestations of its central effects which are utilized in therapy. The sedative effect of its higher doses could be demonstrated in various behavior tests. Doses as high as 250 mg./kg., or above, when injected s.c. caused inhibition of the conditioned reflex in the respective tests and elicited characteristic desynchronization of the EEG (Knoll et al.: Arzneimittelforschung 21, 727-732 (1971)). All these central effects appeared upon adiministration of relatively high doses. In man too, analgesic doses are likely to produce other CNS side effects which, however, do not involve significant problems.
Beagles are much more sensitive to CNS effects than rats, Rhesus monkeys and man. Therefore relatively low doses of Probon are found to cause disturbances of coordination and behavior, as well as ataxia. In case of oral administration these effects appear at doses of above 100 mg./kg. bodyweight, at the 150-200 mg./kg. dose level these symptoms are very marked, and 300 mg./kg. causes the death of the animal.
The analgesic spectrum of Probon significantly differs from that of the major analgesics acting on the opiate receptors (Knoll, J.: Symposium on analgesics, pp 3-18, Academic Press, Budapest 1976, Eds.: J. Knoll and E. S. Vizi). This unique behavior implies the presence of pyridopyrimidine sensitive receptors in the central nervous system, through which these structures exert among others inter alia their analgesic effect.
Based on the above assumption, structure-activity studies have been carried out with the aim to improve the activity spectrum of this series of compounds. It has been found that the new compounds of the formula I are capable of meeting these requirements. An outstanding member of this group is the 2,6-dimethyl-3-ethyl-4-oxo-4H-pyrido[1,2-a]pyrimidine and salts and quaternary salts thereof, particularly in free base form and as the hydrochloride. This compound group and particularly the above-mentioned derivative was found to be a more potent analgesic than Probon in both rats and dogs, while even in high doses failing to elicit the CNS symptoms observed with high doses of Probon in rats and with its low doses in dogs. This appears to support our hypothesis of a selective pyrido[1,2-a]pyrimidine-sensitive receptor in the CNS. The fact that the compounds of the formula I--particularly 2,6-dimethyl-3-ethyl-4-oxo-4H-pyrido[1,2-a]pyrimidine--strongly inhibit the CNS effects of Probon proves the strong affinity of this compound-group to these receptors without possessing specific activity of its own. The lack of toxicity of the compounds of the Formula I in Beagles is considered as a further proof of this hypothesis. Doses as high as 1 g./kg. do not cause toxic changes or death of the animals, but already in a dose as low as 50 mg./kg. it antagonizes the effect of the double of the lethal dose (600 mg./kg.) of Probon. Dogs treated this way showed complete analgesia, without the slightest sign of incoordination or ataxia; no death occured.
The above facts prove that the compounds of the Formula I are new pyrido[1,2-a]pyrimidine derivatives with an activity spectrum substantially differing from that of Probon. It is significantly superior to Probon also from the therapeutic aspect as beside its higher analgesic potency, it is devoid of CNS side effects.
According to a further feature of the present invention there is provided a process for the preparation of compounds of the Formula I and salts and quaternary salts thereof (wherein the substituents have the same meanings as statee before except the provisos which comprises reacting a 2-amino-pyridine of the Formula II ##STR3## or an acid addition salt thereof (wherein R and R.sup.1 have the same meaning as stated above) with a beta-oxo-ester of the formula III ##STR4## (wherein R.sup.2 and R.sup.3 have the same meaning as stated above and R.sup.5 is lower alkyl)--whereby in the case of the preparation of 2,3-dimethyl-, 2-methyl-3-ethyl-, 2,3,7-trimethyl-, 2-methyl-3-ethyl-7-bromo- and 2,6,8-trimethyl-3-ethyl-4-oxo-4H-pyrido[1,2-a]pyrimidine, the reaction is carried out in the mixture of phosphorous oxychloride and polyphosphoric acid--and thereafter, if desired, reducing the compound of the formula IV thus obtained ##STR5## (wherein R.sup.1, R.sup.2, R.sup.3 and R are as stated above) and, if desired, converting a compound of the formula I into another compound of the formula I by methods known per se, if desired, converting a halogenoalkyl substituent into an alkyl substituent by methods known per se and, if desired, converting a compound of the formula I into its salt or quaternary salt or setting it free from its salt or transforming a salt into another salt.
The reaction between the compounds of the formulae II and III is carried out preferably in the presence of an acidic condensing agent. For this purpose phosphoric acid and derivatives thereof, hydrogen halides, p-toluene-sulfonic acid, concentrated sulfuric acid, alkanoic acids, alkanoic acid anhydrides or mixtures thereof can be used. The phosphoric acid derivatives can be orthophosphoric acid, polyphosphoric acid or lower alkyl esters thereof. The reaction may be carried out in the presence or in the absence of a solvent. One may proceed preferably by using phosphorous oxychloride as solvent and a catalytic amount of polyphosphoric acid or a derivative thereof as acidic condensing agent. Thus the desired compounds are obtained in particularly pure form and with high yields.
The reaction mixture may be decomposed by the addition of a lower alkanol (such as methanol or ethanol) Thus a compound of the formula IV (wherein R.sup.1, R.sup.2, R.sup.3 and R have the same meaning as stated above) is obtained as the hydrochloride thereof. This derivative precipitates in crystalline form and can be easily isolated.
According to a preferred embodiment of the process, 0.5 to 1.5 moles of a compound of the formula II and 0.5-1.5 moles of a compound of the formula III are reacted in the presence of 0.5-10.0 moles, preferably 2-5 moles of phosphorous oxychloride and 1-150 g. of polyphosphoric acid (the two latter components are related to 1 mole of a compound of the formula II). Cyclization is carried out at 20.degree.-200.degree. C., preferably at 80.degree.-160.degree. C.
If the reaction mixture is decomposed with water or an alkali, the compound of the formula IV is obtained in the form of the free base.
One may also proceed by reacting the compounds of the formulae II and III in a 2-15-fold amount of polyphosphoric acid. Thus 1 mole of 2-amino-pyridine of the formula II is preferably reacted with 0.5-1.5 moles of a compound of the formula III. The reaction is carried out at 40.degree.-200.degree. C., preferably at a temperature of 60.degree. to 180.degree. C.
The reaction time depends on the temperature and the reactants and is generally 0.1 to 10 hours. The reaction mixture may be worked up by conventional methods e.g. by diluting the reaction mixture with water, neutralizing it with alkali and precipitating the compound of the formula IV a the free base. In this embodiment of the process as solvent, preferably chlorinated hydrocarbons (e.g. chloroform, chlorobenzene etc.), may be used.
If a hydrogen halide is used as acidic condensing agent one may proceed, preferably, by pre-forming the hydrohalide salt of the compound of the formula II and reacting the said salt with the compound of the formula III in the presence of an aromatic tertiary nitrogen compound as solvent.
As hydrogen halide one may use hydrogen chloride, hydrogen bromide or hydrogen iodide, the aromatic tertiary nitrogen containing solvent may be pyridine, picoline, lutidine, quinoline etc. The compound of the formula III may be preferably used in an amount of 0.5-1.5 moles related to 1 mole of a compound of the formula II. The reaction may be carried out at a temperature exceeding 100.degree. C., preferably at the boiling point of the reaction mixture. The reaction having been completed, the solvent is removed--preferably in vacuo--and the residue is crystallized from a suitable solvent. Thus the corresponding hydrogen halide of the compound of the formula IV is obtained.
Alkanoic acids--such as acetic acid and propionic acid--may also be used as acidic condensing agents. This embodiment of our process may be preferably carried out by reacting 0.5 to 1.5 moles of a compound of the formula II with 0.5 to 1.5 moles of a compound of the formula III in the presence of an alkanoic acid under heating, advantageously at the boiling point of the alkanoic acid. Upon evaporation, the mixture and crystallization of the product, the compounds of the formula IV are obtained in the free base form.
By using the above embodiments of our process, the compounds of the formula IV and acid addition salts thereof are obtained in very pure form so that no special purification (e.g. chromatography) is required.
The compounds of the formula IV thus obtained may be subjected to reduction. If catalytic hydrogenation is carried out in the presence of Raney-nickel or a palladium or rhodium catalyst the tetrahydro-pyrido[1,2-a]pyrimidine derivatives of the formula V ##STR6## (wherein R.sup.1, R.sup.2, R.sup.3 and R have the same meaning as stated above) while in the presence of a platinum or platinum oxide catalyst octahydro-pyrido[1,2-a]pyrimidine derivatives of the formula VI ##STR7## (where R.sup.1, R.sup.2, R.sup.3 and R have the same meaning as stated above) are formed.
The tetrahydro-pyrido[1,2-a]pyrimidine derivatives of the formula V may also be converted into the octahydro derivatives of the formula VI by means of hydrogenation in the presence of a platinum or platinum oxide catalyst. This catalytic hydrogenation may be carried out at atmospheric pressure or under elevated pressure. As solvent, e.g. water, alkanols (e.g. methanol, ethanol etc), organic acids (e.g. acetic acid etc), ketones (e.g. acetone, methyl-ethyl-ketone etc), esters (e.g. ethyl acetate etc) or other solvents or mixtures thereof may be used.
A compound of the formula I may be transformed into another compound of the formula I by means of subsequent reactions which may be carried out by methods known per se. Thus a carboxy derivative may be subjected to thermal decarboxylation to give the corresponding derivative in which there is a hydrogen atom at the place of the carboxylic group. A carboxylic acid may be esterified to give the corresponding ester or amidated to yield the optionally substituted acid amide. Thus, for example, 2,6-dimethyl-3-ethyl-9-carboxy-4-oxo-4H-pyrido[1,2-a]pyrimidine may be decarboxylated into the 2,6-dimethyl-3-ethyl-4-oxo-4H-pyrido[1,2-a]pyrimidine. The alkyl groups may also be formed by selective dehalogenation of the corresponding halogenoalkyl derivatives. Thus, for example, 2,6-dimethyl-3-chloroethyl-4-oxo-4H-pyrido[1,2-a]pyrimidine may be transformed into 2,6-dimethyl-3-ethyl-4-oxo-4H-pyrido[1,2-a]pyrimidine by forming the corresponding Grignard compound and subjecting the same to hydrolysis. The compounds of the formula I may be converted into their salts formed with therapeutically acceptable inorganic or organic acids (e.g. hydrochloric, hydrobromic, hydroiodic, sulfuric, nitric, phosphoric, acetic, formic, malic, citric, mandelic acid etc.). Salt formation is carried out by known methods by reacting the compounds of the formula I with an approximately equimolar amount of the corresponding acid in an organic solvent.
The compounds of the formula I may also be converted into their quaternary salts by reacting with usual quaternarizing agents, such as alkyl halides (e.g. methyl bromide, ethyl bromide, ethyl iodide), dialkylsulfates (e.g. dimethyl sulfate, diethyl sulfate etc.), sulfonates (e.g. benzene sulfonate, p-toluene sulfonic acid), trialkyl phosphates, oxonium fluoroborates etc. As the reaction medium the solvents generally used in quaternarization reactions may be used, such as aromatic hydrocarbons (e.g. benzene, toluene etc.), halogenated hydrocarbons (e.g. chloroform, chloro-benzene etc.), ketones (e.g. acetone etc.), alkyl cyanides (e.g. acetonitrile), nitro alkanes (e.g. nitromethane), formamides (e.g. dimethylformamide), dimethylsulfoxide, hexamethylene phosphoric triamide etc.) and mixtures thereof.
The quaternary salts may be subjected to reduction. This may be carried out by methods known per se. One may use catalytic hydrogenation or complex metal hydrides (e.g. sodium borohydride, sodium cyano borohydride, sodium-bis-(ethoxy-methoxy)-aluminumhydride etc.). A preferred embodiment of this process resides in the use of complex metal hydrides in a solvent which depends on the reducing agent (e.g. water, aliphatic alcohols, aromatic hydrocarbons etc.).
According to a further feature of the present invention there are provided pharmaceutical compositions comprising as active ingredient a compound of the formula I wherein
R is hydrogen, halogen, lower alkyl, nitro, hydroxy, amino, lower alkoxy, carboxy or a derivative of the carboxy group;
R.sup.1 is hydrogen, halogen or lower alkyl;
R.sup.2 is an alkyl group having 1 to 16 carbon atoms;
R.sup.3 is an alkyl group having 1 to 16 carbon atoms, a C.sub.7-12 aralkyl group optionally halogeno-substituted on the aromatic ring; or a cycloalkyl-alkyl group having 6 to 12 carbon atoms;
R.sup.4 is a lone pair of electrons or a hydrogen atom or a lower alkyl group;
the dotted lines represent optional bonds)
or a salt or quaternary salt thereof in admixture with suitable inert pharmaceutical carriers and/or excipients. The compositions may be formulated in solid (e.g. tablets, capsules, dragees, pills, coated pills etc), or liquid (e.g. solution, emulsion or suspension) form. The compositions contain conventional carriers such as talc, magnesium stearate, water, polyethylene glycol etc. The compositions may also contain usual additives (e.g. emulsifying agents, disintegrating agents, buffers etc.). The compositions may be prepared by methods of pharmaceutical industry known per se.
The compositions of the present invention may contain, in addition to the compounds of the Formula I, further therapeutically active substances e.g. other analgesics (such as morphine), benzomorphane derivatives (e.g. phenazocine, pentazocine), phenyl-piperidine derivatives (e.g. petidine, nisentyle).
The daily active ingredient dosage may vary between wide ranges and depends on the specific circumstances of the application in caption. As a guideline it may be stated that the daily oral dosage is approximately between 1 and 300 mg. and may be administered as such or in several portions, while the parenteral daily dosage amounts to about 0.1 to 100 mg.
The compounds of the formula I possess useful analgesic and morphine-potentiating properties and are valuable analgesics having a novel action mechanism. In Table I the morphine-potentiating effect of these compounds is demonstrated.
Table I______________________________________ i.v. dose for potentiating the effect of 5 mg. LD.sub.50 of morphine,Test compound mg./kg. mmole/kg.______________________________________2,3,6-trimethyl-4-oxo-4H- 0.780 0.066pyrido[1,2-a]pyrimidine . HCl2,6-dimethyl-3-ethyl-4-oxo- 0.796 0.0214H-pyrido[1,2-a]pyrimidine . HCl2-methyl-3-ethyl-4-oxo-4H- 1.070 0.012pyrido[1,2-a]pyrimidine . HCl3,6-dimethyl-2-ethyl-4-oxo-4H- 0.120 0.0019pyrido[1,2-a]pyrimidine . HCl2-methyl-3-n-propyl-4-oxo-4H- 0.502 0.0105pyrido[1,2-a]pyrimidine . HCl2,6-dimethyl-3-n-propyl-4-oxo- 0.316 0.00254H-pyrido[1,2-a]pyrimidine . HClProbon.sup.R 0.607 0.069______________________________________
The following Table proves the outstanding analgesic properties of 2,6-dimethyl-3-ethyl-4-oxo-4H-pyrido[1,2-a]pyrimidine.hydrochloride (referred to further as Compound A) over the chemically related 2-methyl-3-ethyl-4-oxo-4H-pyrido[1,2-a]pyrimidine.HCl (Compound B) and 2,6,8-trimethyl-3-ethyl-4-oxo-4H-pyrido[1,2-a]pyrimidine.HCl (Compound C). The analgesic effect was tested on the hot-plate and algolytic tests. The results are summarized in Table II.
Table II______________________________________ Hot plate test Algolytic testTest compound ED.sub.50 mg./kg. p.o. ED.sub.100 mg./kg. p.o.______________________________________A 68 420B 330 cannot be achievedC 580 cannot be achieved______________________________________
Table III contains further comparative date concerning Compounds A, B and C.
Table III__________________________________________________________________________ ED.sub.50 (mg./kg.) Narcosis ED.sub.50 (mg./kg.) algolytic potentLD.sub.50 (mg./kg.) hot-plate (+5mg./kg. ED.sub.500 %Test i.v. s.c. p.o. i.v. s.c. p.o. morphine) (mg./kg.)__________________________________________________________________________A 190 520 690 74 68 effective per se 58 98 s.c. 420 s.c. 19 s.c. 8.6 s.c. 52 s.c. 25 p.o.B 280 620 1000 100 180 300 2.75 i.v. 18 s.c. 40 i.v. 98 p.o.C 120 820 1500 49 120 580 210 s.c. 100 i.v. 290 p.o.__________________________________________________________________________
The above data show the outstanding effects of Compound A which surpass significantly the activity of the chemically related compounds. The instant compounds proved to be active in the algolytic test too.
The following Table IV contains test results in which the analgesic activity of the compounds of the present invention is compared to that of Probon.
Table IV__________________________________________________________________________ LD.sub.50 (rats) Hot plate test mg./kg. ED.sub.50 mg./kg. (rats)Test compound p.o. i.v. s.c. p.o. i.v. s.c.__________________________________________________________________________2,6-dimethyl-3-ethyl-4-oxo-4H-pyrido[1,2-a]pyrimidine . 690 190 520 68 74HCl2-methyl-3-ethyl-4-oxo-4H- 1000 280 620 300 100 180pyrido[1,2-a]pyrimidine . HCl2,6,8-trimethyl-3-ethyl-4-oxo-4H-pyrido[1,2-a] 1500 120 820 580 49 120pyrimidine . HCl2,6-dimethyl-3-n-propyl-4-oxo-4H-pyrido[1,2-a] 1000 -- 1200 -- -- 48pyrimidine . HCl2,9-dimethyl-3-ethyl-4-oxo-4H-pyrido[1,2-a]pyrimidine . 820 -- -- 310 -- --HCl2,7-dimethyl-3-ethyl-4-oxo-4H-pyrido[1,2-a]pyrimidine . 900 175 800 500 75 150HCl2-methyl-3-ethyl-7-chloro-4-oxo-4H-pyrido[1,2-a] 1100 -- -- 98 -- --pyrimidine . HCl2,3,6-trimethyl-4-oxo-4H-pyrido[1,2-a]pyrimidine . HCl -- 175 -- 87 -- --2-methyl-3-n-butyl-4-oxo-4H-pyrido[1,2-a]pyrimidine . HCl 1100 -- -- 251 -- --2,6-dimethyl-3-n-butyl-4-oxo-4H-pyrido[1,2-a]pyrimidine . 1100 -- -- 340 -- --HCl1,6-dimethyl-3-ethoxy-carbonyl-4-oxo-4H-6,7,8,9- 1600 220 -- 220 50 --tetrahydro-pyrido[1,2-a]pyrimidinium-methosulfate(Probon)__________________________________________________________________________
The test methods used are disclosed in the following publications:
Hot plate test: Woolfe and McDonald J. Pharm. 80, 300 (1944) modified by Porszasz and Herr: Kiserletes Orvostudomany 2, 292 (1950).
Algolytic test: J. Knoll et al: Animal and Clinical Pharmacological Techniques in Drug Evaluation Eds. Siegler, P. E. and Meyer J. II. Year Book Medical Pub. Chicago (1967) pages 305-321
Toxicity: Litchfield J. T. and Wilcoxon: J. Pharmacol. Sci 54 (1965) 888.

Further details of the present invention are to be found in the Examples without limiting the scope of our invention to the Examples. The starting material used in our process are known compounds.
EXAMPLE 1
10.8 g. of 2-amino-6-methylpyridine are reacted with 14.4 g. of ethyl 2-methylacetacetate in a mixture of 46 g. of phosphorus oxychloride and 7.0 g. of polyphosphoric acid at 100.degree. C. for 3 hours. The initially violent hydrogen chloride gas evolution gradually ceases. The reaction mixture is treated with 100 ml. of ethanol at a temperature of 70.degree. to 80.degree. C., whereupon the mixture is allowed to stand in a refrigerator overnight. The precipitated crystals are filtered off, washed with ethanol and dried. 20.2 g. (90%) of 2,3,6-trimethyl-4-oxo-4H-pyrido[1,2-a]pyrimidine hydrochloride are obtained, melting at 215.degree. to 220.degree. C. after recrystallization from a mixture of ethanol and ether.
Analysis for C.sub.11 H.sub.12 N.sub.2 O.HCl: Calculated: C=58.81%, H=5.83%, N=12.47%, Cl=15.78%. Found: C=58.48%, H=5.83%, N=12.28%, Cl=15.62%.
Following the procedure described above but using ethyl 2-n-propylacetacetate in place of ethyl 2-methylacetacetate, 2,6-dimethyl-3-n-propyl-4-oxo-4H-pyrido[1,2-a]pyrimidine hydrochloride is obtained, melting at 180.degree. to 185.degree. C.
Analysis for C.sub.13 H.sub.16 N.sub.2 O.HCl: Calculated: C=61.78%; N=6.78%, N=11.08%, Cl=14.03%. Found: C=61.52%, N=6.98%, N=11.03%, Cl=13.95%.
Following the procedure described above but using ethyl-2-n-butylacetacetate in place of ethyl-2-methylacetacetate, 2,6-dimethyl-3-n-butyl-4-oxo-4H-pyrido[1,2-a]pyrimidine hydrochloride is obtained, melting at 216.degree. to 217.degree. C.
Analysis for C.sub.14 H.sub.18 N.sub.2 O.HCl: Calculated: C=63.03%, H 2 7.17%, N=10.50%, Cl=13.28%. Found: C=62.65%, H=6.96%, N=10.68%, Cl=13.46%.
Following the procedure described above but using ethyl-2-n-decylacetacetate in place of ethyl 2-methylacetacetate, 2,6-dimethyl-3-n-decyl-4-oxo-4H-pyrido[1,2-a]pyrimidine hydrochloride is obtained, melting at 185.degree. to 187.degree. C.
Analysis for C.sub.20 H.sub.30 N.sub.2 O.HCl: Calculated: C=68.45%, H=8.90%, N=7.98%, Cl=10.10%. Found: C=68.35%, H=8.72%, N=7.92%, Cl=10.15%.
Following the procedure described above but using ethyl-2-benzylacetacetate in place of ethyl 2-benzylacetacetate, 2,6-dimethyl-3-benzyl-4-oxo-4H-pyrido[1,2-a]pyrimidine hydrochloride is obtained, melting at 186.degree. to 191.degree. C.
Analysis for C.sub.17 H.sub.16 N.sub.2 O.HCl: Calculated: C=67.89%, H=5.70%, N=9.31%, Cl=11.79%. Found: C=68.25%, H=6.13%, N=9.48%, Cl=11.06%.
Following the procedure described above but using ethyl 2-isobutylacetacetate in place of ethyl 2-methylacetacetate, 2,6-dimethyl-3-isobutyl-4-oxo-4H-pyrido[1,2-a]pyrimidine hydrochloride is obtained, melting at 178.degree. to 185.degree. C.
Analysis for C.sub.14 H.sub.18 N.sub.2 O.HCl: Calculated: C=63.03%, H=7.17%, N=10.50%, Cl=13.28%. Found: C=62.65%, H=6.86%, N=10.68%, Cl=13.46%.
Following the procedure described above but using ethyl-2-methyl-3-oxo-valerate in place of ethyl-2-methylacetacetate, 3,6-dimethyl-2-ethyl-4-oxo-4H-pyrido[1,2-a]pyrimidine hydrochloride, melting at 196.degree. to 202.degree. C. is obtained.
Analysis for C.sub.12 H.sub.14 N.sub.2 O.NCl: Calculated: C=60.38%, H=6.33%, N=11.73%, Cl=14.85%. Found: C=60.11%, H=6.70%, N=11.68%, Cl=14.56%.
Following the procedure described above but using ethyl-2-ethylacetacetate in place of ethyl 2-methylacetacetate and 2-aminopyridine instead of 2-amino-6-methylpyridine, 2-methyl-3-ethyl-4-oxo-4H-pyrido[1,2-a]pyrimidine hydrochloride, melting at 185.degree. to 190.degree. C. is obtained.
Analysis for C.sub.11 H.sub.12 N.sub.2 O.HCl: Calculated: C=58.81%, H=5.83%, N=12.47%, Cl=15.78%. Found: C=58.41%, H=5.83%, N=12.62%, Cl=15.65%.
Following the procedure described above but using 2-aminopyridine and ethyl-2-n-propylacetacetate as starting compounds, 2-methyl-3-n-propyl-4-oxo-4H-pyrido[1,2-a]pyrimidine hydrochloride, melting at 210.degree. to 215.degree. C. is obtained.
Analysis for C.sub.12 H.sub.14 N.sub.2 O.HCl: Calculated: C=60.38%, H=6.33%, N=11.73%, Cl=14.85%. Found: C=60.45%, H=6.20%, N=11.82%, Cl=14.80%.
Following the procedure described above but using 2-aminopyridine and ethyl-2-n-butylacetacetate as starting compounds, 2-methyl-3-n-butyl-4-oxo-4H-pyrido[1,2-a]pyrimidine hydrochloride, melting at 220.degree. to 222.degree. C. is obtained.
Analysis for C.sub.13 H.sub.16 N.sub.2 O.HCl: Calculated: C=61.78%, H=6.78%, N=11.08%, Cl=14.03%. Found: C=61.89%, H=6.80%, N=11.00%, Cl=13.95%.
Following the procedure described above but using 2-aminopyridine and ethyl-2-n-decylacetacetate as starting compounds, 2-methyl-3-n-decyl-4-oxo-4H-pyrido[1,2-a]pyrimidine hydrochloride is obtained. m.p.=200.degree. to 202.degree. C.
Analysis for C.sub.19 H.sub.28 N.sub.2 O.HCl: Calculated: C=67.74%, H=8.68%, N=8.31%, Cl=10.52%. Found: C=67.81%, H=8.75%, N=8.19%, Cl=10.40%.
Following the procedure described above but using 2-aminopyridine and ethyl-2-benzylacetacetate as starting compounds, 2-methyl-3-benzyl-4-oxo-4H-pyrido[1,2-a]pyrimidine hydrochloride is obtained, m.p.=180.degree. to 190.degree. C.
Analysis for C.sub.16 H.sub.14 N.sub.2 O.HCl: Calculated: C=67.02%, H=5.27%, N=9.77%, Cl=12.36%. Found: C=67.14%, H=5.25%, N=9.90%, Cl=11.98%.
Following the procedure described above that using 2-aminopyridine and ethyl-2-[(4-chlorophenyl)-methyl]-acetacetate as starting compounds, 2-methyl-3-[(4-chlorophenyl)-methyl]-4-oxo-4H-pyrido[1,2-a]pyrimidine hydrochloride is obtained, m.p.=175.degree. to 180.degree. C.
Analysis for C.sub.16 H.sub.13 N.sub.2 OCl.HCl: Calculated: C=67.25%, H=4.94%, N=9.80%, Cl=12.41%. Found: C=67.01%, H=5.03%, N=9.86%, Cl=12.25%.
EXAMPLE 2
10.8 g. of 2-amino-6-methylpyridine are reacted with 15.8 g. of ethyl-2-ethylacetacetate in a mixture of 46. g. of phosphorus oxychloride and 7 g. of polyphosphoric acid at 120.degree. to 130.degree. C. for 3 hours. The initially violent hydrogen chloride gas evolution gradually ceases. The reaction mixture is treated with 100 ml. of ethanol at 70.degree. to 80.degree. C., whereupon the mixture is allowed to stand in a refrigerator overnight. The precipitated crystals are filtered off, washed with ethanol and dried. 22 g. (92%) of 2,6-dimethyl-3-ethyl-4-oxo-4H-pyrido[1,2-a]pyrimidine hydrochloride are obtained, m.p.=233.degree. C. after recrystallization from a mixture of ethanol and ether.
Analysis for C.sub.12 H.sub.14 N.sub.2 O.HCl: Calculated: C=60.38%, H=6.33%, N=11.74%, Cl=14.85%. Found: C=60.44%, H=6.40%, N=11.90%, Cl=14.61%.
EXAMPLE 3
12.8 g. of 2-amino-5-chloropyridine are reacted with 15.8 g. of ethyl-2-ethylacetacetate in a mixture of 46 g. of phosphorus oxychloride and 7 g. of polyphosphoric acid at 120.degree. to 130.degree. C. for 3 hours. The initially violent hydrogen chloride gas evolution gradually ceases. The reaction mixture is treated with 100 ml. of water at 70.degree. to 80.degree. C. Upon cooling the pH-value of the mixture is adjusted to neutral with sodium carbonate. The aqueous reaction mixture is shaken with four 100-ml. portion of chloroform. The combined chloroform solutions, dried on sodium sulphate, are evaporated and ethyl acetate is distilled through the residue. 20.2 g. (91%) of 2-methyl-3-ethyl-7-chloro-4-oxo-4H-pyrido[1,2-a]pyrimidine are obtained, melting at 114.degree. to 116.degree. C. after recrystallization from a mixture of ethanol and ether.
Analysis for C.sub.11 H.sub.11 N.sub.2 OCl: Calculated: C=59.33%, H=4.98%, N=12.58%, Cl=15.92%. Found: C=59.20%, H=5.02%, N=12.39%, Cl=16.07%.
Following the procedure described above but using 2-amino-3-methylpyridine as an amine component, 2,9-dimethyl-3-ethyl-4-oxo-4H-pyrido[1,2-a]pyrimidine is obtained, melting at 90.degree. to 92.degree. C.
Analysis for C.sub.12 H.sub.14 N.sub.2 O: Calculated: C=71.26%, H=6.98%, N=13.85%. Found: C=71.20%, H=6.97%, N=13.70%.
Following the procedure described above but using 2-aminopyridine and ethyl-2-(cyclohexylmethyl)-acetacetate as starting compounds, 2-methyl-3-(cyclohexylmethyl)-4-oxo-4H-pyrido[1,2-a]pyrimidine is obtained, m.p.=112.degree. to 114.degree. C.
Analysis for C.sub.16 H.sub.20 N.sub.2 O: Calculated: C=74.97%, H=7.86%, N=10.93%. Found: C=75.10%, H=7.86%, N=10.95%.
Following the procedure described above but using 2-amino-6-methylpyridine and ethyl-2-(cyclohexylmethyl)-acetacetate as starting compounds 2,6-dimethyl-3-(cyclohexylmethyl)-4-oxo-4H-pyrido[1,2-a]pyrimidine is obtained, m.p.=124.degree. to 126.degree. C.
Analysis for C.sub.17 H.sub.22 N.sub.2 O: Calculated: C=75.52%, H=8.20%, N=10.36%. Found: C=75.40%, H=8.22%, N=10.29%.
EXAMPLE 4
4.77 g. of 2,6-dimethyl-3-ethyl-4-oxo-4H-pyrido[1,2-a]pyrimidine hydrochloride are dissolved in 50 ml. of water and the pH-value of the mixture is adjusted to 7 with a 10% aqueous sodium carbonate solution. The reaction mixture is shaken with four 25-ml. portions of chloroform, the chloroform extracts are combined, dried over sodium sulphate and evaporated. Ethyl acetate is distilled through the residue. 4.0 g. (99%) of 2,6-dimethyl-3-ethyl-4-oxo-4H-pyrido[1,2-a]pyrimidine are obtained, melting at 127.degree. to 128.degree. C. after recrystallization from a mixture of ethanol and ether.
Analysis for C.sub.12 H.sub.14 N.sub.2 O: Calculated: C=71.26%, H=6.98%, N=13.85%. Found: C=71.09%, H=6.98%, N=13.67%.
Following the procedure described above but starting from 2-methyl-3-n-decyl-4-oxo-4H-pyrido[1,2-a]pyrimidine hydrochloride, 2-methyl-3-n-decyl-4-oxo-4H-pyrido[1,2-a]pyrimidine is obtained, m.p.=66.degree. to 67.5.degree. C.
Analysis for C.sub.19 H.sub.28 N.sub.2 O: Calculated: C=75.96%, H=9.39%, N=9.32%. Found: C=76.11%, H=9.40%, N=9.34%.
EXAMPLE 5
4.45 g. of 2-methyl-3-ethyl-7-chloro-4-oxo-4H-pyrido[1,2-a]pyrimidine are dissolved in ethanol, with heating, then 25 ml. of a 28% by weight solution of hydrogen chloride in ethanol is added to the solution obtained. Upon the precipitated crystals are filtered off and washed with ethanol. 5.01 g. (97%) of 2-methyl-3-ethyl-7-chloro-4-oxo-4H-pyrido[1,2-a]pyrimidine hydrochloride are obtained, m.p.=176.degree. to 180.degree. C.
Analysis for C.sub.11 H.sub.11 N.sub.2 OCl.HCl: Calculated: C=50.98%, H=4.57%, N=10.81%, Cl=13.68%. Found: C=50.82%, H=4.74%, N=10.92%, Cl=13.44%.
EXAMPLE 6
4.04 g. of 2,6-dimethyl-3-ethyl-4-oxo-4H-pyrido[1,2-a]pyrimidine are dissolved in 50 ml. of ethanol and the solution is hydrogenated in the presence of 2 g. of Raney-nickel catalyst, previously washed to anhydrous with ethanol. Hydrogenation is performed under atmospheric pressure. In about seven hours the calculated amount of hydrogen is used up and the hydrogen consumption drops rapidly to zero. The catalyst is filtered off and the ethanol solution is evaporated. 4.10 g. (99.5%) of 2,6-dimethyl-3-ethyl-4-oxo-6,7,8,9-tetrahydro-4H-pyrido[1,2-a]pyrimidine are obtained as a pale-yellow non-crystallizing oil, which can be distilled under a pressure of 25 mmHg of 190.degree. C.
Analysis for C.sub.12 H.sub.18 N.sub.2 O: Calculated: C=69.87%, H=8.80%, N=13.58%. Found: C=69.82%, H=8.96%, N=13.62%.
When in the procedure described above a 10% palladium on carbon catalyst is used instead of Raney-nickel, a calculated amount of hydrogen is consumed in 10 hours and 2,6-dimethyl-3-ethyl-4-oxo-6,7,8,9-tetrahydro-4H-pyrido[1,2-a]pyrimidine is obtained as a non-crystallizing oil.
EXAMPLE 7
A mixture of 10.8 g. of 2-amino-6-methyl-pyridine, 15.8 g. of ethyl-2-ethylacetacetate and 100 g. of polyphosphoric acid is stirred at 100.degree. C. for 1.5 hours. The reaction mixture is diluted with 75 to 100 ml. of water, then its pH-value is adjusted to 7 with a 10% aqueous sodium hydroxide solution. The precipitated crystals are filtered off, washed with water and dried. 17.2 g. (85%) of 2,6-dimethyl-3-ethyl-4-oxo-4H-pyrido[1,2-a]pyrimidine are obtained, melting at 127.degree. to 128.degree. C. after recrystallization from a mixture of ethanol and ether. When the product is admixed with the product of Example 6, no melting point decrease is observed.
EXAMPLE 8
Following the procedure described in Example 7 but using 0.02 moles of 2-amino-3-hydroxypyridine and 0.02 moles of ethyl-2-ethylacetacetate, 2-methyl-3-ethyl-9-hydroxy-4-oxo-4H-pyrido[1,2-a]pyrimidine is obtained, melting at 128.degree. C. after recrystallization from a 70% aqueous ethanol solution. Yield: 73%.
Analysis for C.sub.11 H.sub.12 N.sub.2 O.sub.2 : Calculated: C=64.69%, H=5.92%. Found: C=64.90%, H=6.15%.
EXAMPLE 9
Following the procedure described in Example 1 but reacting 0.02 moles of 2-amino-3-hydroxypyridine and 0.02 moles of ethyl-2-ethylacetacetate, 2-methyl-3-ethyl-9-hydroxy-4-oxo-4H-pyrido[1,2-a]pyrimidine hydrochloride is obtained, melting at 175.degree. to 178.degree. C. after recrystallization from a mixture of ethanol and ether. Yield: 59%.
Analysis for C.sub.11 H.sub.12 N.sub.2 O.sub.2.HCl: Calculated: C=55.12%, H=5.47%, Cl.sup.- =14.79%. Found: C=55.22%, H=5.51%, Cl.sup.- =14.67%.
EXAMPLE 10
Following the procedure described in Example 7 but reacting 0.02 moles of 2-amino-3-hydroxypyridine and 0.02 moles of ethyl-2-benzylacetacetate, 2-methyl-3-benzyl-9-hydroxy-4-oxo-4H-pyrido[1,2-a]pyrimidine is obtained, melting at 124.degree. to 125.degree. C., after recrystallization from ethanol. Yield: 70%.
Analysis for C.sub.16 H.sub.14 N.sub.2 O.sub.2 : Calculated: C=72.16%, H=5.30%. Found: C=71.97%, H=5.41%.
EXAMPLE 11
Following the procedure described in Example 7 but reacting 0.02 moles of 2-amino-5-nitropyridine and 0.02 moles of ethyl-2-ethylacetacetate-2-methyl-3-ethyl-7-nitro-4-oxo-4H-pyrido[I,2-a]pyrimidine is obtained. Yield: 38%. The product is contaminated with a small amount of starting 2-amino-5-nitropyridine, which can easily be eliminated by crystallization from ethanol. Melting point after two subsequent crystallizations from ethanol: 163.degree. to 164.degree. C.
Analysis for C.sub.11 H.sub.11 N.sub.3 O.sub.3 : Calculated: C=56,65%, H=4.75%. Found: C=56.50%, H=4.60%.
EXAMPLE 12
Following the procedure described in Example 3 but reacting 0.02 moles of 2-amino-5-nitropyridine and 0.02 moles of ethyl-2-ethylacetacetate, 2-methyl-3-ethyl-7-nitro-4-oxo-4H-pyrido[1,2-a]pyrimidine is obtained, melting at 164.degree. to 165.degree. C. after two subsequent recrystalizations from ethanol. Yield: 51%. The product does not show any melting point depression when admixed with the product of Example 11.
EXAMPLE 13
0.02 moles of 2-amino-4-methylpyridine hydrochloride and 0.03 moles of ethyl-2-ethylacetacetate in 50 ml. of pyridine are refluxed for 16 hours. The solvent and the excess amount of ketoester are distilled off under reduced pressure and the residue is crystallized from a mixture of ethanol and ether. 2,8-dimethyl-3-ethyl-4-oxo-4H-pyrido[1,2-a]pyrimidine hydrochloride is obtained, melting at 192.degree. to 198.degree. C. Yield: 39%. After recrystallization from ethanol the product melts at 195.degree. to 199.degree. C.
Analysis for C.sub.12 H.sub.14 N.sub.2 O. HCl: Calculated: C=60.38%, H=6.33%, Cl.sup.- =14.85%. Found: C=60.41%, H=6.38%, Cl.sup.- =14.67%.
EXAMPLE 14
0.02 moles of 2-aminopyridine hydrobromide and 0.03 moles of ethyl-2-n-propylacetacetate are reacted as described in Example 13 to afford 2-methyl-3-n-propyl-4-oxo-4H-pyrido[1,2-a]pyrimidine hydrobromide, Yield: 49%. The product sublimates at 210.degree. C. after recrystallization from ethanol.
Analysis for C.sub.12 H.sub.14 N.sub.2 O.HBr: Calculated: C=50.90%, H=5.34%. Found: C=50.81%, H=5.20%.
The free base deliberated from the hydrogen bromide salt in a conventional manner melts at 57.degree. to 58.degree. C. The 2-methyl-3-n-propyl-4-oxo-4H-pyrido[1,2-a]pyrimidine obtained is crystallized from n-hexane. The product does not give any melting point depression when admixed with the base set free from 2-methyl-3-n-propyl-4-oxo-4H-pyrido[1,2-a]pyrimidine hydrochloride.
Analysis for C.sub.12 H.sub.14 N.sub.2 O: Calculated: C=71.26%, H=6.98%. Found: C=71.32%, H=6.86%.
EXAMPLE 15
Following the procedure described in Example 13 but reacting 0.02 moles of 2-aminopyridine hydroiodide and 0.03 moles of ethyl-2-n-propylacetacetate 2-methyl-3-n-propyl-4-oxo-4H-pyrido[1,2a]pyrimidine hydroiodide is obtained, melting at 200.degree. to 210.degree. C. after recrystallization from ethanol. Yield: 53%.
Analysis for C.sub.12 H.sub.14 N.sub.2 O.HI: Calculated: C=43.66%, H=4.58%. Found: C=43.41%, H=4.67%.
The free base deliberated from the hydrogen iodide salt in a conventional manner melts at 58.degree. to 59.degree. C. The product does not give any melting point depression when admixed with 2-methyl-3-n-propyl-4-oxo-4H-pyrido[1,2-a]pyrimidine obtained in Example 14.
EXAMPLE 16
0.02 moles of 2-aminonicotinic acid and 0.02 moles of ethyl-2-ethylacetacetate in 20 g. of polyphosphoric acid are stirred at 145.degree. C. for one hour. The reaction mixture is diluted with 10 ml. of water and its pH-value is adjusted to neutral with a 10% aqueous sodium hydroxide solution. The precipitated oily product is extracted with three 25-ml. portions of chloroform, the chloroform extracts are combined, dried and evaporated. 2-methyl-3-ethyl-9-carbonyl-4-oxo-4H-pyrido[1,2-a]pyrimidine is obtained, melting at 177.degree. to 179.degree. after recrystallization from ethanol. Yield: 41%.
Analysis for C.sub.12 H.sub.12 N.sub.2 O.sub.3 : Calculated: C=62.02%, H=5.21%. Found: C=62.10%, H=5.13%.
EXAMPLE 17
Following the procedure described in Example 7 but reacting 0.02 moles of 2-amino-4-ethoxycarbonyl-pyridine and 0.02 moles of ethyl-2-ethylacetacetate 2-methyl-3-ethyl-8-ethoxycarbonyl-4-oxo-4H-pyrido[1,2-a]pyrimidine is obtained, melting at 94.degree. to 96.degree. C. after crystallization from ethanol. Yield: 64%.
Analysis for C.sub.14 H.sub.16 N.sub.2 O.sub.3 : Calculated: C=64.60%, H=6.20%. Found: C=64.44%, H=6.24%.
EXAMPLE 18
0.02 moles of 2-amino-4-ethoxycarbonylpyridine and 0.02 moles of ethyl-2-ethylacetacetate are stirred in a mixture of 10 ml. of phosphorus oxychloride and 2 g. of polyphosphoric acid at 120.degree. C. for 2 hours. The reaction mixture is treated with 20 ml. of ethanol at 70.degree. to 80.degree. C., whereupon it is neutralized with a 10% (w/v) aqueous sodium hydroxide solution with ice cooling. The ethanol is evaporated, the residue is extracted with four 25-ml. portions of chloroform and the combined extracts are dried and evaporated. The evaporation residue is triturated with ether to give crystalline 2-methyl-3-ethyl-8-ethoxycarbonyl-4-oxo-4H-pyrido[1,2-a]pyrimidine, melting at 95.degree. to 96.degree. C. Yield: 42%. The product does not give any melting point depression when admixed with the product of Example 17.
EXAMPLE 19
0.01 moles of 2,6-dimethyl-3-ethyl-4-oxo-4H-pyrido[1,2-a]pyrimidine are dissolved in 20 ml. of acetone, 0.03 moles of methyl-iodide are added and the mixture is kept in a bomb tube at 150.degree. C. for 24 hours. The solution is then concentrated to 10 ml. and allowed to stand for 24 hours. 1,2,6-trimethyl-3-ethyl-4-oxo-4H-pyrido[1,2-a]pyrimidine iodide precipitates, melting at 203.degree. to 206.degree. C. after recrystallization from ethanol. Yield: 86%.
Analysis for C.sub.13 H.sub.17 IN.sub.2 O: Calculated: C=45.37%, H=4.98%. Found: C=45.16%, H=4.81%.
EXAMPLE 20
Following the procedure described in Example 6, starting from 0.02 moles of 2-methyl-3-ethyl-4-oxo-4H-pyrido[1,2-a]pyrimidine colorless, viscous 2-methyl-3-ethyl-6,7,8,9-tetrahydro-4-oxo-4H-pyrido[1,2-a]pyrimidine is obtained, which can be distilled at 146.degree. to 148.degree. C./6 mmHg.
Yield (using Raney-nickel as a catalyst): 96%, (using palladium on charcoal as a catalyst): 97%.
After a short standing the product crystallizes.
Analysis for C.sub.11 H.sub.16 N.sub.2 O: Calculated: C=68.72%, H=8.39%. Found: C=68.67%, H=8.40%.
EXAMPLE 21
0.01 moles of 2,6-dimethyl-3-ethyl-4-oxo-4H-pyrido[1,2-a]pyrimidine are dissolved in 20 ml. of acetone, 0.03 moles of methyl iodide are added and the mixture is kept in a bomb tube at 150.degree. C. for 24 hours. The solution is evaporated to dryness, the residue is dissolved in 15 ml. of methanol and a solution of 0.05 moles of sodium tetrahydroborate (III) in 10 ml. of water is added. After 4 hours the methanol is distilled off and the aqueous phase is extracted with three 20-ml. portions of chloroform. The organic phase is dried, evaporated and added to the oily substance obtained are 10 ml. of ethanol saturated with hydrochloric acid. 1,2,6-trimethyl-3-ethyl-1,2,3,6,7,8,9,9a-octahydro-4-oxo-4H-pyrido[1,2-a]pyrimidine hydrochloride is obtained, which crystallizes when triturated with ether. The product obtained after recrystallization from a mixture of acetone and ether sublimates over 206.degree. C. Yield: 41%.
Analysis for C.sub.13 H.sub.20 N.sub.2 O.HCl: Calculated: C=60.81%, H=8.24%, Cl.sup.- =13.81%. Found: C=60.64%, H=8.12%, Cl.sup.- =13.96%.
EXAMPLE 22
10 g. of 3-ethyl-2,6-dimethyl-4-oxo-4H-pyrido[1,2-a]pyrimidine are dissolved in 100 ml. of ethanol and 12 g. of fumaric acid in 100 ml. of ethanol are added. The mixture is brought to the boil and then cooled. The precipitated crystals are filtered off, washed with a small portion of ethanol and dried. 12.5 g. (78.5%) of di-(3-ethyl-2,6-dimethyl-4-oxo-4H-pyrido[1,2-a]pyrimidinium)-fumarate are obtained, melting at 185.degree. to 186.degree. C. after recrystallization from ethanol.
Analysis for C.sub.28 H.sub.32 N.sub.4 O.sub.6 : Calculated: C=64.60%, H=6.20%, N=10.76%. Found: C=64.35%, H=6.24%, N=10.40%.
EXAMPLE 23
10 g. of 3-ethyl-2,6-dimethyl-4-oxo-4H-pyrido[1,2-a]pyrimidine are dissolved in 100 ml. of ethylmethyl ketone with heating and to the solution obtained a solution of 12 g. of maleic acid in 100 ml. of ethylmethyl ketone is added. The reaction mixture is brought to a boil, then cooled. The precipitated crystals are filtered off and washed with a small portion of ethylmethyl ketone. 14.0 g. (87.9%) of hydrogen-(3-ethyl-2,6-dimethyl-4-oxo-4H-pyrido[1,2-a]pyrimidinium)maleate are obtained, melting at 137.degree. to 138.degree. C. after recrystallization from ethanol.
Analysis for C.sub.16 H.sub.18 N.sub.2 O.sub.5 : Calculated: C=60.36%, H=5.70%, N=8.80%. Found: C=60.35%, H=5.72%, N=9.65%.
EXAMPLE 24
10 g. of 3-ethyl-2,6-dimethyl-4-oxo-4H-pyrido[1,2-a]pyrimidine are dissolved in 100 ml. of acetone with heating and a solution of 7 g. of salicyc acid in 100 ml. of acetone is added. The reaction mixture is brought to a boil, then cooled. The precipitated crystals are filtered off, washed with acetone and dried. 11.5 g. (67.6%) of 3-ethyl-2,6-dimethyl-4-oxo-4H-pyrido[1,2-a]pyrimidinium salicylate are obtained, melting at 126.degree. to 128.degree. C. after recrystallization from ethanol.
Analysis for C.sub.19 H.sub.20 N.sub.2 O.sub.4 : Calculated: C=67.04%, H=5.92%, N=8.22%. Found: C=67.50%, H=5.94%, N=8.25%.
EXAMPLE 25
10 g. of 3-ethyl-2,6-dimethyl-4-oxo-4H-pyrido[1,2-a]pyrimidine are dissolved in 30 ml. of ethanol with heating and to the solution obtained as solution of 19.2 g. of citric acid in 100 ml. of ethanol is added. The reaction mixture is brought to a boil, then cooled. The precipitated crystals are filtered off, washed with ethanol and dried. 18.2 g. (92.4%) of hydrogen-(3-ethyl-2,6-dimethyl-4-oxo-4H-pyrido[1,2-a]pyrimidinium)-citrate are obtained, melting at 136.degree. to 137.degree. C. after recrystallization from ethanol.
Analysis for C.sub.18 H.sub.22 N.sub.2 O.sub.8 : Calculated: C=54.83%, H=5.62%, N=7.10%. Found: C=55.08%, H=5.70%, N=7.01%.
EXAMPLE 26
10 g. of 3-ethyl-2,6-dimethyl-4-oxo-4H-pyrido[1,2-a]pyrimidine are dissolved in 100 ml. of acetone with heating and to the solution obtained a solution of 13.4 g. of D,L-malic acid in 100 ml. of acetone is added. The reaction mixture is brought to a boil and then cooled. The precipitated crystals are filtered off, washed with acetone and dried. 11.5 g. (69.4%) of hydrogen-(3-ethyl-2,6-dimethyl-4-oxo-4H-pyrido[1,2-a]pyrimidinium)-2-hydroxysuccinate are obtained, melting at 141.degree. to 142.degree. C. after recrystallization from ethanol.
Analysis for C.sub.28 H.sub.34 N.sub.4 O.sub.7 : Calculated: C=62.44%, H=6.36%, N=10.40%. Found: C=62.47%, H=6.76%, N=10.43%.
EXAMPLE 27
10.0 g. of 3-ethyl-2,6-dimethyl-4-oxo-4H-pyrido[1,2-a]pyrimidine are dissolved in 50 ml. of ethanol with heating and to the solution obtained 2.8 ml. of a 96 to 97% by weight aqueous sulphuric acid are added. The mixture is brought to a boil, then cooled. The precipitated crystals are filtered off, washed with ethanol and dried. 5 g. (33%) of hydrogen-(3-ethyl-2,6-dimethyl-4-oxo-4H-pyrido[1,2-a]pyrimidinium)-sulphate are obtained, melting at 199.degree. to 200.degree. C. after recrystallization from ethanol.
Analysis for C.sub.12 H.sub.16 N.sub.2 O.sub.5 S: Calculated: C=47.99%, H=5.40%, N=9.33%. Found: C=48.31%, H=5.51%, N=9.55%.
EXAMPLE 28
Following the procedure described in Example 2 but using 2-amino-4-methylpyridine as a starting amino-pyridine compound, 3-ethyl-2,8-dimethyl-4-oxo-4H-pyrido[1,2-a]pyrimidinium hydrochloride is obtained, melting at 195.degree. to 200.degree. C. after recrystallization from ethanol. Yield: 64%.
Analysis for C.sub.12 H.sub.14 N.sub.2 O.HCl: Calculated: C=60.38%, H=6.33%, N=11.74%, Cl=14.85%. Found: C=60.42%, H=6.38%, N=11.82%, Cl=14.67%.
EXAMPLE 29
Following the procedure described in Example 2 but using 2-amino-4,6-dimethylpyridine as a starting amino-pyridine, 3-ethyl-2,6,8-trimethyl-4-oxo-4H-pyrido[1,2-a]-pyrimidinium hydrochloride, melting at 198.degree. to 205.degree. C. after recrystallization from ethanol.
Analysis for C.sub.13 H.sub.16 N.sub.2 O.HCl: Calculated: C=61.78%, H=6.78%, N=11.08%, Cl=14.03%. Found: C=62.08%, H=6.81%, N=11.17%, Cl=13.82%.
EXAMPLE 30
Following the procedure described in Example 2 but using 2-ethyl-3-oxocapric acid ethylester as an oxo-ester, 3-ethyl-6-methyl-3-n-propyl-4-oxo-4H-pyrido[1,2-a]pyrimidinium hydrochloride is obtained, melting at 160.degree. to 165.degree. C. after recrystallization from ethanol. Yield: 75%.
Analysis for C.sub.14 H.sub.18 N.sub.2 0.HCl: Calculated: C=63.03%, H=7.18%, N=10.50%, Cl=13.25%. Found: C=63.28%, H=7.32%, N=10.58%, Cl=13.15%.
EXAMPLE 31
A mixture of 2.16 g. of 2-amino-5-methylpyridine and 3.16 g. of ethyl-2-ethylacetacetate in a mixture of 4.6 ml. of phosphorus oxychloride and 1.4 g. of polyphosphoric aicd is stirred at 120.degree. to 130.degree. C. for 45 minutes. The initially violent gas evolution gradually ceases. The reaction mixture is treated with 20 ml. of ethanol and is crystallized upon cooling and scratching. The precipitated crystals are filtered off. The 4.6 g. of hydrochloric acid salt are dissolved in 20 ml. of water and the solution is neutralized with a 20% (w/v) aqueous sodium carbonate solution. The precipitated crystals are filtered off, washed with water and dried. 2 g. (49%) of 3-ethyl-2,7-dimethyl-4-oxo-4H-pyrido[1,2-a]pyrimidine are obtained, melting at 154.degree. to 156.degree. C. After recrystallization from methanol.
Analysis for C.sub.12 H.sub.14 N.sub.2 O: Calculated: C=71.42%, H=6.98%, N=13.85%. Found: C=71.42%, H=7.08%, N=13.91%.

Pyrido[1,2-a]pyrimidine derivatives

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Shur et al., Chemical Abstracts, vol. 69, 52090y (1968).
Brown et al., Chemical Abstracts, vol. 75, 48839f (1971).
Yale et al., Chemical Abstracts, vol. 86 29741d (1/31/77).