AU6631590A - Novel cephalosporin compounds and processes for preparation thereof - Google Patents

Description

NOVEL CEPHALOSPORIN COHPOUNDS AND

PROCESSES FOR PREPARATION THEREOF

Field of the Invention

The present invention relates to novel cephalosporin compounds, pharmaceutically acceptable non-toxic salts thereof, and physiologically hydrolyzable esters, hydrates and solvates thereof, which possess potent and broad antibacterial activities. The invention also relates to processes for preparing the sane, and to pharmaceutical compositions containing the sane as active ingredients.

Background of the Invention

Antibiotics of cephalosporin series are widely used in therapy for treatment of diseases which are caused by general pathogenic bacteria in human beings and animals. It has been known that such antibiotics are useful for the treatment of diseases caused by bacteria exhibiting the resistance to other antibiotics, e.g. penicillin - resistant bacteria, and for treatment of penicillin - sensitive patients.

In most circumstances it is desirable to employ antibiotics showing broad antibacterial activities against both Gram-positive and

Gran-negative bacteria. In this regard, there have been made many studies in developing a variety of cephalosporin antibiotics with broad-spectrum antibiotic activities.

For example, in GB patent No. 1,399,086 there are disclosed ιany cephalosporin derivatives which are shown by the formula

wherein

R is hydrogen or an organic group ;

R^a is an etherifying monovalent organic group linked to the

oxygen atom through a carbon atom ;

B is -S- or and

P is an organic group.

After the invention of these compounds, there were many attempts to develop antibiotic compounds having more improved properties, to certain bacteriums, especially to Gram-negative bacteria.

GB patent No. 1,522,140 discloses cephalosporin antibiotic compounds of the formula(B) which exist as syn isomers, or as a mixture of syn and anti isomers wherein the syn isomers are present in at least 90%,

wherein

R' is a furyl or thienyl group ;

R" is a C_1~4 alkyl, C_5~7 cycloalkyl, furylnethyl or thienylmethyl group ; and

R''' is hydrogen or a carbamoyl, carboxymethyl, sulfonyl or methyl group. The foregoing cephalosporin compounds have high antibacterial activities against a range of Gram-positive and Gram-negative bacteria, and particularly high stability to β-lactamases produced by various Gram-negative bacteria. Moreover, they are very stable in vivo.

Recently, there have been efforts to prepare new antibiotics having improved and broadened antibiotic spectrums while showing potent antibiotic activities, especially against Gram-negative bacteria. Consequently a large number of cephalosporin antibiotics with analogous structures, to those above, have been developed.

As a part of said efforts, an acylamido group has been introduced into the 7-position of the cephem nucleus as shown in the foregoing formula(B) and certain groups have been introduced into the 3-position thereof.

For example, in BE patent No. 852,427 there are reported a number of cephalosporin compounds having antibiotic activities which are shown by the foregoing formula(A) wherein the R is substituted with various organic groups including 2-aminothiazol, the oxygen atom of the oxyimino group is directly bonded to an aliphatic hydrocarbon group, which aliphatic hydrocarbon group may itself be substituted with a carboxy group. The substituent in 3-position of such compounds is an acetoxymethyl, hydroxymethyl, formyl group, or an optionally substituted hetero cyclic thiomethyl group.

Also, in US patent No. 4,390,534 to Psutomu Terachi et al, there are reproted new cephem compounds of the formula wherein

R¹ is amino or a protected amino group ;

R² is hydrogen, acyl, substituted or unsubstituted aryl, substituted alkyl, alkenyl, alkynyl, substituted or unsubstituted cycloalkyl, cycloalkenyl, or a O- or S-containing 5-membered hetero cyclic group ;

R³ is hydrogen or alkyl ;

R⁴ is an acyloxyalkyl, acylthioalkyl, substituted or unsubstituted pyridiniumalkyl, substituted or unsubstituted heterocyclic thioalkyl, alkyl, hydroxy, or a substituted or unsubstitued thiazoliumalkyl group, or halogen ;

R⁵ is carboxy or a protected carboxy group, wherein R⁵ is COO- when R⁴ is a substituted or unsubstituted pyridiniumalkyl group or a substituted or unsubstituted thiazoliunalkyl group ; and the dotted line "- - - - - - " represents a single bond or a double bond.

While the P of the aforesaid GB patent No. 1,399,086 or the R⁴ of the aforesaid US patent No.4,390,534 are defined very broadly as an organic group or a substituted or unsubstituted heterocyclic thioalkyl group, respectively, there is not therein mentioned the heart of the present invention, that is a compound having (1-substituted-4,6-diaminopyrimidinium- 2-yl)thiomethyl group introduced into 3-position of the cephem nucleus. Also, European patent application No. 62,321 discloses cephem compounds of the formula(D) and pharmaceutically acceptable salts thereof, and their intermediates of the fonula(D')

whe rein

R¹ is amino or a protected amino group ;

R² is a substituted or unsubstituted lower aliphatic hydrocarbon group, or a cycloalkenyl group ; and

is a substituted or unsubstituted heterocyclic cation group

containing one or more nitrogen atoms ;

wherein

R¹ and R² are the same as defined in the formula(D), respectively ; R⁴ is a protected carboxyl group ; and

X- is an acid residue.

In European patent application NO.74,563, the cephem compounds of the formula(E) and their salts are proposed as antibiotic compounds

wherein

R¹ is amino or a protected amino group ;

R² is a protected or unprotected lower aliphatic hydrocarbon group, cyclo(lower)alkyl, or eyelo(lower)alkenyl group ;

R³ is (lower)alkylamino, N-protected(lower)alkylamino, di(lower) alkylamino, sulfo(lower)alkylaιino, hydroxy(lower)alkylamino, N-protected hydroxy(lower)alkylanino, acyloxy(lower)alkyl, (lower)alkoxy(lower)alkoxy(lower)alkyl, di(lower)alkylamino (lower)alkyl, (lower)alkylthio(lower)alkyl, (lower)alkylthio, (lower)alkoxy(lower)alkoxy, (lower)alkoxy, hydroxy(lower)alkoxy, acyl(lower)alkyl, hydroxy(lower)alkylthio, di(lower)alkylamino (lower)alkylthio, N-containing unsaturated 5-meιbered heterocyclic group, N-containing unsaturated 5-membered heterocyclic thio group, or N-containing unsaturated 5- or 6-meιbered heterocyclic (lower)alkyl group which may be optionally substituted with suitable substituent(s) ; and

R⁴ is hydrogen or a (lower)alkyl group.

There are disclosed cephem compounds of the formula(F) and their salts in European patent application No.47,977

wherein

n is an integer of 0 or 1 ;

An is amino or a substituted amino group ;

T is a thiadiazoly moiety, where one carbon atom is bonded to Am and the other carbon atom is bonded to the group of -C(=N-O-R²)- ;

R² is hydrogen, a substituted or unsubstituted carbamoyl group, a

cycloalkyl group, or a substituted or unsubstituted carbanoyl group ; and

R¹ is a substituted or. unsubstituted thiazolium group, a substituted or unsubstituted pyrazolium group, a tri(lower)alkyl ammonium group or a pyridinium group of the following formula

[wherein

R^a is (lower)alkyl [which is substituted with a substituent selected from the group consisting of cycloalkyl, nethyl, hydroxy, alkoxy, halogen, cyano, carbamoyl, carboxyl and sulfonyl], (lower)alkenyl or carboxy-substituted (lower)alkenyl, (lower) alkylthio or carboxy-substituted (lower)alkylthio, amino or mono-substituted amino [wherein the substituent is selected from the group consisting of (lower) alkyl, (lower)alkanoyl or aminobenzenesulfonyl], di(lower)alkylamino, carbamoyl [which is substituted by (lower)alkyl, hydroxy(lower)alkyl, (lower)alkoxy, hydroxy or cyano], di(lower)alkylcarbamoyl, thiocarbamoyl, cycloalkyl, phenyl, hydroxy, (lower)alkoxy, halogen, (lower) alkoxycarbonyl, (lower)alkanoyloxy, (lower)alkanoyl, carboxy, sulfocyano, nitro, or a hydroxysulfo(lower)alkyl group ;

R^b is hydrogen, a carbamoyl group, or a group selected from the groups defined for R^a ; and

R^c is hydrogen or a group selected from the groups as defined in the R^a. As described above, there are a variety of cephem compounds whose 7-positions are substituted by a substituted aminothiadiazole ring. However, there are no reports about the most important characteristic of the present invention that is a (l-substituted-4,6-diaminopyrimidinium-2-yl)thiomethyl group introduced into the 3-position of the cephem nucleus.

Summary of the Invention

An objective of the present invention is to provide new antibiotic cephalosporin compounds of the formula(I), pharmaceutically acceptable non-toxic salts thereof, and metabolically labile esters and solvates thereof

wherein

R¹ is a C_1~4 alkyl (preferably methyl or ethyl), C_3~4 alkenyl (preferably allyl), C_{3 ~4} alkynyl (perferably propargyl) group, or -C(R^a)(R^b)CO₂H, wherein R^a and R^b, same or different, are a hydrogen atom or a C_1~4 alkyl group, or R^a and R^b form a C_3~7 cycloalkyl group with the carbon atom to which they are linked ;

R² is a C_1~4 alkyl (perferably a straight alkyl group such as methyl, ethyl, n-propyl or n-butyl), C_3~4 alkenyl (preferably allyl), C_3~7 cycloalkyl, substituted or unsubstituted anino or a substituted or unsubstituted phenyl (preferably phenyl, 4- hydroxyphenyl, 4-chlorophenyl, 3,4-dimethylphenyl, 2,4- dimethylphenyl or 2,6-dimethyoxyphenyl) group ;

R³ is hydrogen or a C_1~4 alkyl group(preferably methyl or ethyl) ; and Q is N or CH.

Another objective of the present invention is to provide processes for preparing the cephalosporin compounds of formula(I). A further objective of the present invention is to provide pharmaceutical compositions comprising one or more of the cephalosporin compounds of formula(I) as active ingredients.

Description of the Proferred Embodments

The new cephalosporin compounds of the present invention are either syn isomers or mixtures of syn and anti isomers which contain at least 90% of the syn isomer and not more than 10% of the anti isomer. Also, when the R¹ group of formula(I) compounds is -C(R^a)(R^b)CO₂H, wherein R^a and R^b are diffierent, the carbon atom to which R^a and R^b are linked becomes an asymmetrical center, these compounds being diastereoisomers. Therefore, the present invention also includes such diastereoisomers of cephalosporin compounds of fornula (I), and mixtures thereof.

Also, the solvates including hydrates of the compounds(I) are included within the scope of the invention. In addition, the compounds of the formula(I) according to the present invention may exist in tautomeric forms and such tautomers are also included within the scope of the invention. Namely, when Q of the formula (I) is a carbon atom, the aπinothiazolyl group undergoes tautomerism to fon a iminothiazolinyl group, its tautomer, as follows :

When the Q of the formula (I) is a nitrogen atom, the aainothiadiazolyl group forms iainothiadiazolinyl groups, its tautomers by tautomerism as follows :

The compounds of the fonula (I) also include the following resonance structures (I') and (I'') :

Suitable pharmaceutically acceptable salts of the object compounds (I) are conventional non-toxic salts and may include an inorganic salt, for example, a metal salt such as an alkali metal salt(e.g., sodium salt, potassium salt, etc.) and an alkaline earth metal salt(e.g., calcium salt, magnesium salt, etc.), ammonium salt, etc.; an organic salt, for example, an organic amine salt(e.g., trimethylamine salt, triethylamine salt, pyridine salt, procaine salt, picoline salt, dicyclohexylamine salt, N.N'-dibenzylethylene-diamine salt, N-methylglucamine salt, diethanolamine salt, triethanolamine salt, tris(hydroxymethylamino) methane salt, phenylethylbenzylamine salt ; dibenzylethylenediamine salt, etc.) etc.; organic carboxylic or sulfonic acid salt(e.g., formate, acetate, maleate, tartrate, nethanesulfonate, benzenesulfonate, toluenesulfonate etc.); an inorganic acid salt(e.g., hydrochloride, hydrobromide, sulfate, phosphate, etc.) ; a salt with a basic or acidic anino acid(e.g., arginine, aspartic acid, glutamic acid, lysine, etc.) and the like.

The physiologicall hydrolyzable esters of the compounds (I) may include, for example, indanyl, phthalidyl, methoxynethyl, pivaloyloxymethyl, glycyloxymethyl, phenylglycyloxymethyl or 5-methyl-2-oxo-1,3-dioxolan-4-yl esters, and other physiologically hydrolyzable esters which have been widely used in the technical fields of penicillin and cephalosporin antibiotics. These esters can be prepared in accordance with known methods.

The cephalosporin compounds of the formula(I) exhibit high antibacterial activities against both Gram-positive and Gram-negative bacteria, and are especially useful in the therapheutic and prophylactic treatment of bacterial infections in human beings and animals. The present invention also includes within its scope pharmaceutical compositions comprising one or more of the compounds ( I ) according to the present invention as active ingredients, in association with pharmaceutically acceptable carriers, excipients or other additives.

The antibiotic compounds(I) of the invention may be formulated for administration, which nay be presented in unit dose form or in multidose containers. The compositions may take various forms such as solutions, suspensions or emulsions in oily or aqueous vehicles, which can contain conventional additives such as dispersing agents, suspending agents, stabilizing agents, and the like. Alternatively, the active ingredient may be formed into a dried powder that can be normally dissolved in an aqueous solution of sterile, pyrogen-free water, before use. The compounds(I) may be also formulated into suppositories containing conventional suppository bases such as cocoa butter or other glycerides.

The pharmaceutical compositions in unit dose form, preferably comprise about from 50 to 1,500 mg of the active ingredient, depending on the age and body weight of the patient, the nature and the severity of the illness, and so on. In general it has proved advantageous to administer the active compounds in an amount of about 500 to 5,000 mg per day in order to achieve the desired results, depending on the routes and frequency of administration. In case of intramuscular or intravenous administrations for adult human treatment, the dose of about 150 to 3,000 mg per day is thought sufficient, but it may be increased in case of treatment for specific infections caused by some strains. If desired, the compounds(I) can be administered in combination with other antibiotics such as penicillins or other cephalosporins.

The compounds of the present invention as described above, exhibit potent and broad antibacterial activities against Gram-positive bacteria and a variety of Gram-negative bacteria as well, particulary against Pseudomonas. Also, these compounds have high stability to β-lactanases produced by a number of Gram-negative bcteria.

Examples of especially preferred compounds (I) are the compounds (I-1) and (I-15) of the formula(I) wherein R¹ is -C(CH₃)₂CO₂H, R² is methyl or amino, R³ is hydrogen, and Q is CH, and their pharmaceutically acceptable non-toxic salts. These compounds (I-1) and (1-15) posseses excellent antibacterial activities, especially against Pseudomonas.

Further examples of preferred compounds( I ) of the present invention are as follows :

R¹ R² R³ Q

-C(CH₃)₂CO₂H -CH₃ H CH

-C(CH₃)₂CO₂H -CH₂CH₃ H CH

-C(CH₃)₂CO₂H -NH₂ H CH

-C(CH₃)₂CO₂H -CH₃ -CH₃ CH

-CH(CH₃)CO₂H -CH₃ H CH

-CH(CH₃)CO₂H -CH₂CH₃ H CH

-CH(CH₃)CO₂H -CH₂CH₂CH₃ H CH

-C(CH₃)CO₂H -NH₂ H CH

-CH₂C≡CH -CH₃ H CH

-CH₂C≡CH -CH₂CH₃ H CH

-CH₂C≡CH -NH₂ H CH

-CH₂CH₃ -NH₂ H CH

-CH₂CH₃ -CH₂ H N

-CH₂CH₃ -NH₂ H N

-CH₂CO₂H -CH₃ H CH

-CH₂CO₂H -CH₂CH₃ H CH The cephalosporin compounds (I), pharmaceutically acceptable non-toxic salts thereof, or physiologically hydrolyzable esters or solvates (including hydrates) thereof may be prepared by reacting the compounds of the formula (II) with the compounds of the formula(HI) in the presence of a solvent, and then, if necessary, removing the amino protecting group and/or the carboxyl protecting group and/or reducing the S-oxide [that is, S→(O)_n] by a known method, before or after said reaction. This process also constitutes a further aspect of the invention.

Wherein

R¹, R², R³ and Q are the sane as defined above ;

n is an integer of 0 or 1 ;

R⁴ is hydrogen or an amino protecting group ;

R⁵ is a C_1~4 alkyl, C_3~4 alkenyl or C_3~4 alkynl group, or -C(R^a)(R^b)CO₂(R^c), wherein R^a and R^b, same or different, are a hydrogen atom or a C_1~4 alkyl group, or R^a and R^b may form a C_3~7 cycloalkyl group with the carbon atom to which they are linked ; and R^c is hydrogen or a carboxyl protecting group ;

R³ is a hydrogen atom or a carboxyl protecting group ; and

L is a leaving group.

The amino protecting group may include acyl, substituted or unsubstituted aryl(lower)alkyl(e.g. benzyl, diphenylaethyl, triphenylnethyl and 4-nethoxybenzyl), halo(lower)alkyl(e.g. trichloronethyl and trichloroethyl), tetrahydropyranyl, substituted phenylthio, substituted alkylidene, substituted aralkylidene or substituted cyclolidene. The acyl group as an amino protecting group may include, for example, C_1~5 (lower) alkanoyl ( e.g. formyl and acetyl), C_2~5 alkoxycarbonyKe.g. nethoxycarbonyl and ethoxycarbonyl), (lower)alkanesulfonyl (e.g. nethanesulfonyl and ethanesulfonyl), or aryl(lower)alkoxycarbonyKe.g. benzyloxycarbonyl), where the acyl group can be substituted by 1~3 substituent(s) such as halogen, hydroxy, cyano or nitro. In addition, the amino protecting group may include reaction products obtained fron amino groups and silane, boron or phosphorus compounds.

The carboxyl protecting group as R^c of R⁵ or R⁵ may include for exanple, (lower) alkylesters (e.g. methylester and t-butylester), (lower) alkenylesters (e.g. vinylester and allylester), (lower) alkoxy (lower) alkylesters (e.g. methoxymethylester), (lower) alkylthio (lower) alkylesters (e.g. lethylthiomethylester), halo(lower)alkylesters (e.g. 2,2,2- trichloroethylester), substituted or unsubstituted aralkylesters (e.g. benzylester and p-nitrobenzylester) or silylesters, which can be selected after consideration of the chemical property of the desired compounds(I). It is desired that the aforementioned amino or carboxyl protecting groups may be readily removed under mild reaction conditions by a known method.

The leaving group L may include, for examples, halogen such as chlorine or fluorine, an (lower)alkanoyloxy group such as acetoxy, a

(lower)alkanesulfonyloxy group such as aethanesulfonyloxy, an arenesulfonyloxy group such as p-toluenesulfonyloxy, an alkoxycarbonyloxy groups and the like.

The starting laterials of the compounds(II) are known as intermediates conventionally employed for the preparation of cephalosporin compounds. The dotted line of the formula(II) represents a single bond or a double bond, and therefore, the compounds of the formula(II) may be the compounds of the formula(II-a), or compounds of the formula (Il-b), or mixtures thereof :

wherein

n, R⁴, R⁵, R⁶, Q and L are the same as defined above. The compounds of the formula(II) can be prepared by activating the compounds of the fonula(IV) or their salts with an acylating agent, and reacting with the compounds of the formula(V), as follows :

wherein

n, R⁴, R⁵, R⁶, Q and L are the same as defined above ; and the dotted line of the formula(V) presents a single bond or a double bond, so that the compounds of the formula(V) may be the compounds of the formula(V-a), or compounds of the fonuIa(V-b), or lixtures thereof

wherein n, R^β and L and the same as defined above. In the preparation of the objective compounded ), the compounds of the formula(II) are used preferably in an amount of from 1 to 2 equivalent(s) based on 1 equivalent of the compounds of the fornula(III).

Amino or acid protecting groups can be readily removed by a conventional deprotection methods which are well known in the field of cephalosporin antibiotics. For example, acid- or base-hydrolysis or reduction are generally applicable. For further example, when the protecting group is an amido group, it is feasible to subject such compounds to imino-halogenation and imino-etherification, and then, follow by hydrolysis. Acid hydrolysis is preferable applicable to removal of such groups as tri(di)phenylmethyl or alkoxycarbonyl, and is carried out in the presence of an organic acid such as formic acid, trifluoroacetic acid, or p-tolueneacetic acid or an inorganic acid such as hydrochloric acid or the like.

The reaction for introducing the compounds(III) into the 3-position of compounds(II) to prepare compounds(I) is carried out in the presence of a solvent such as water, or a mixed aqueous solvent of water and a water-mixable solvent. In the reaction, the pH of the solvent should range from 5 to 8, but preferably from 6 to 7.5. An appropriate water-mixable solvent is acetonitrile or acetone.

Also, the reaction may be carried out at 40° to 100ºC, preferably 60º to 80ºC.

To stabilize reaction products and their intermediates, one or more salts selected from the group consisting of sodium iodide, potassiun iodide, sodium bromide, potassium bromide and potassiun thiocyanate can be used as stabilizing agents. On the other hand, the separation and purification of the compounds(I) can be carried out using a known method such as recrystallization, column chromatography over silica gel or ion-exchange chromatography.

The cephalosporin compounds(I) of the present invention, and their non-toxic salts, preferably alkali metal salts, alkaline earth metal salts, inorganic acid salts or amino acid salts, show potent antibacterial activities against a variety of general pathogenic bacteria including Gram-negative and Gram-positive bacteria, therefore, they are especially useful in theraphy for treatment of bacterial infections in human beings and animals.

In order to illustrate the usefulness of the invented compounds, the minimal inhibitory concentrations(MIC) thereof against standard strains and against clinically isolated-strains, were determined and compared with Ceftazidime of a known compound.

Also, the in vitro antibacterial activity was determined by a twofold dilution method as described below :

That is, the two-fold serial dilutions of the compound were made and dispersed in Huller-Hinton agar medium. 2 μl of standard test strain which had the 10⁷ CFU per ml was inoculated on the medium, and was incubated at 37ºC for 20 hours. The results of the MIC tests are shown in Table 1.

The results of the MIC tests against clinically separated-strains are shown in Table 2.

Specific examples of the compounds of formula(I) provided by this invention are shown below : I - 1 : 7-[ (Z)-2-(2-aminothiazol-4-yl)-2-(2-carboxylprop-2-oxyimino) acetamido]-3-(4,6-diamino-1-methylpyrimidinium-2-yl)thiomethyl-3- cephem-4-carboxylate

I - 2 : 7-[(Z)-2-(2-aainothiazol-4-yl)-2-(2-carboxylprop-2-oxyimino)

acetamino]-3-(4,6-diamino-1-ethylpyrimidinium-2-yl)thiomethyl-3- cephem-4-carboxylate

- 3 : 3-(1-allyl-4,6-diaιinopyrimidinium-2-yl)thiomethyl-7-[(Z)-2-(2- aminothiazol-4-yl)-2-(2-carboxyprop-2-oxyimino)acetamido]-3-cephem- 4-carboxylate

I - 4 : 7-[ (Z)-2-(2-aminothiazol-4-yl)-2-(1-carboxyeth-1-oxyimino) acetamido]-3-(4,6-diamino-1-methylpyrimidinium-2-yl)thiomethyl-3- cephem-4-carboxylate

I - 5 : 7-[ (Z)-2-(2-aminothiazol-4-yl)-2-(1-carboxyeth-1-oxyimino)

acetamido]-3-(4,6-diamino-1-ethylpyrimidinium-2-yl)thiomethyl-3- cephem-4-carboxylate

I - 6 : 3-(1-allyl-4,6-diaιinopyrimidinium-2-yl)thiomethyl-7-[ (Z)-2-(2- aminothiazol-4-yl)-2-(1-carboxyeth-1-oxyimino)acetamido]-3-cephem -4-carboxylate

I - 7 : 7-[(Z)-2-(2-aminothiazol-4-yl)-2-(carboxymethoxyimino)acetamido]- 3-(4,6-diamino-1-methylpyrimidinium-2-yl)thiomethyl-3-cephem-4- carboxylate

I - 8 : 7-[(Z)-2-(2-aminothiazol-4-yl)-2-(carboxymethoxyimino)acetamido]- 3-(4,6-diamino-1-ethylpyrimidinium-2-yl)thiomethyl-3-cephem-4- carboxylate

I - 9 : 3-(1-allyl-4,6-diaminopyriιidinium-2-yl)thioιethyl-7-[(Z)-2- aninothiazol-4-yl)-2-(carboxymethoxyimino)acetamido]-3-cephem-4- carboxylate

I - 10 : 7-[ (Z)-2-(2-aπinothiazol-4-yl)-2-(ιethoxyiιino)acetaιido]-3-(4,6- diamino-1-aethylpyrinidinium-2-yl)thiomethyl-3-cephen-4-carboxylate

I - 11 : 7-[ (Z)-2-(2-aminothiazol-4-yl)-2-(ethoxyimino)acetamido]-3-(4 ,6- diaιino-1-methylpyriaidinium-2-yl)thiomethyl-3-cephem-4-carboxylate

I - 12 : 7-[(Z)-2-(2-aminothiazol-4-yl)-2-(ethoxyimino)acetamido]-3-(4,6- diaιino-1-ethylpyriιidinium-2-yl)thiomethyl-3-cephem-4-carboxylate

I - 13 : 7-[ (Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(2-carboxyprop-2- oxyiaino)acetamido]-3-(1,4,6-triaminopyrimidinium-2-yl)thiomethyl- 3-cephem-4-carboxylate

I - 14 : 7-[ (Z)-2-(2-aminothiazol-4-yl)-2-(l-carboxyeth-1-oxyimino)

acetamido]-3-(1,4,6-triaminopyrimidinium-2-yl)thiomethyl-3-cephem- 4-carboxylate

I - 15 : 7-[(Z)-2-(2-aminothiazol-4-yl)-2-(2-carboxyprop-2-oxyimino)

acetaιido]-3-(1,4,6-triaminopyrimidinium-2-yl)thiomethyl-3-cephem -4-carboxylate

I - 16 : 7-{ (Z)-2-(2-aιinothiazol-4-yl)-2-(ethoxyiιino)acetaιido]-3-(1,4, 6-triaiinopyrimidinium-2-yl)thiomethyl-3-cephem-4-carboxylate

I - 17 : 7-[ (Z)-2-(5-aaino-1,2,4-thiadiazol-3-yl)-2-(ethoxyimino)

acetamido]-3-(1,4,6-triaminopyriaidinium-2-yl)thiomethy1-3-cephem -4-carboxylate

I -18 : 7-[(Z)-2-(2-aιinothiazol-4-yl)-2-(2-propyn-1-oxyimino)acetamido]- 3-(1,4,6-triaminopyrimidiniua-2-yl)thiomethyl-3-cephem-4- carboxylate

I - 19 : 7-[ (Z)-2-(2-aBinothiazol-4-yl)-2-(Bethoxyiιino)acetaaido]-3-(1,4 , 6-triaminopyrimidinium-2-yl)thiomethyl-3-cephem-4-carboxylate

I - 20 : 7-[ (Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(ethoxyimino)

acetamido]-3-(4,6-diamino-1-methylpyrimidinium-2-yl)thiomethyl-3- cephem-4-carboxylate

I - 21 : 7-[ (Z)-2-(5-amino-l,2,4-thiadiazol-3-yl)-2-(ethoxyimino)

acetaiido]-3-(4,6-diamino-1-ethylpyriiidinium-2-yl)thiomethyl-3- cephem-4-carboxylate

I - 22 : 7-[(Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(ethoxyimino)acetamido]- 3-(4,6-diamino-1-propylpyrimidiniun-2-yl)thiomethyl-3-cephem-4- carboxylate

I - 23 : 3-(1-allyl-4,6-diaminopyrimidinium-2-yl)-7-[ (Z)-2-(5-amino-1,2,4- thiadiazol-3-yl)-2-(ethoxyimino)acetamido]-3-cephem-4-carboxylate

I - 24 : 7-[(Z)-2-(5-amino-1 ,2,4-thiadiazol-3-yl)-2-(methoxyimino)acetamido]- 3-(4,6-diamino-1-methylpyrimidinium-2-yl)thiomethyl-3-cephem-4- carboxylate

I - 25 : 7-[(Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(Bethoxyimino)acetamido]- 3-(4,6-diamino-1-ethylpyrimidiniua-2-yl)thiomethyl-3-cephem-4- carboxylate

I - 26 : 7-[(Z)-2-(5-amino-l,2,4-thiadiazol-3-yl)-2-(2-carboxyprop-2- oxymino)acetamido]-3-(4,6-diamino-1-methylpyrimidinium-2-yl) thiomethyl-3-cephem-4-carboxylate

I - 27 : 7-[(Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(2-carboxyprop-2- oxyimino)acetamido]-3-(4,6-diamino-1-ethylpyrimidinium-2-yl) thiomethyl-3-cephem-4-carboxylate

I-28 : 7-[(Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(2-carboxyprop-2- oxyimino)acetamido]-3-(4,6-diamino-1-propylpyrimidinium-2-y1) thiomethyl-3-cephem-4-carboxylate

I - 29 : 7-[ (Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(2-carboxyprop-2- oxyiaino)acetamido]-3-(1-butyl-4,6-diaminopyrimidinium-2-yl) thiomethyl-3-cephem-4-carboxylate

H₃

I - 30 : 7-[ (Z)-2-(2-aminothiazol-4-yl)-2-(2-carboιyprop-2-oxyimino)

acetamido]-3-(4,6-diamino-1,5-dimethylpyrimidinium-2-yl) thiomethyl -3-cephem-4-carboxylate

I - 31 : 7-[(Z)-2-(2-aminothiazol-4-yl)-2-(2-carboxyprop-2-oxyimino) acetamido]-3-(4,6-diamino-5-ethyl-1-methylpyrimidinium-2-yl) thiomethyl-3-cephem-4-carboxylate

I - 32 : 7-[(Z)-2-(2-aminothiazol-4-yl)-2-(2-carboxyprop-2-oxyimino)

acetamido]-3-(4,6-diaιino-1-ethyl-5-methylpyrimidinium-2-yl)

I - 33 : 7-[(Z)-2-(2-aminothiazol-4-yl)-2-(2-carboxyprop-2-oxyimino)

acetamido]-3-(4,6-diamino-1,5-diethylpyrimidinium-2-yl)thiomethyl -3-cephem-4-carboxylate

I - 34 : 7-[ (Z)-2-(2-aminothiazol-4-yl)-2-(2-carboxyprop-2-oxyimino) acetamino]-3-(5-methyl-1 ,4,6-triaminopyrimidinium-2-yl)thiomethyl -3-cephem-4-carboxylate

I - 35 : 7-[ (Z)-2- (2-aminothiazol-4-yl)-2-(2-carboxyprop-2-oxyimino)

acetamido]-3-(4,6-dianino-1-phenylpyrimidinium-2-yl)thiomethyl-3- cephem-4-carboxylate

I - 36 : 7-[(Z)-2-(2-aminothiazol-4-yl)-2-(2-carboxyprop-2-oxyinino)

acetamido]-3-[1-(4-hydroxyphenyl)-4,6-diaminopyrimidinium-2-yl]- thiomethyl-3-cephem-4-carboxylate

I - 37 : 7-[ (Z)-2-(2-aminothiazol-4-yl)-2-(carboxymethoxyimino)acetamido] -3-(4,6-diamino-1-phenylpyrimidinium-2-yl)thiomethyl-3-cephem-4- carboxylate

I - 38 : 7-[ (Z)-2-(2-aminothiazol-4-yl)-2-(1-carboxyeth-1-oxyimino)

acetamido]-3-(4,6-diamino-1-phenylpyrimidinium-2-yl)thiomethyl-3- cephem-4-carboxylate

I - 39 : 7-[ (Z)-2-(2-aminothiazol-4-yl)-2-(ethoxyimino)acetamido]-3-(4 , 6- diamino-1-phenylpyrimidinium-2-yl)thiomethyl-3-cephem-4-carboxylate

I- 40 : 7-[(Z)-2-(2-aminothiazol-4-yl)-2-(ethoxyiιino)acetamido]-3-[1-(4- chlorophenyl)-4,6-diaminopyrimidinium-2-yl]thiomethyl-3-cephem-4- carboxylate

1 - 41 : 7-[ (Z)-2-(2-aminothiazol-4-yl)-2-(2-carboxyprop-2-oxyimino)

acetamido]-3-[4,6-diamino-1-(2,4-dinethylphenyl)-pyrimidinium-2- yl]thiomethyl-3-cephem-4-carboxylate

1 - 42 : 7-[ (Z)-2-(2-aminothiazol-4-yl)-2-(ethoxyiιino)acetamido]-3-(4,6- diamino-1-(2,4-dimethylphenyl)-pyrimidinium-2-yl]-thiomethyl-3- cephem-4-carboxylate

I - 43 : 7-[ (Z)-2-(2-aminothiazol-4-yl)-2-(2-carboxyprop-2-oxyimino) acetamido]-3-[4,6-diamino-1-(2,6-dimethoxyphenyl)-pyrimidiniun-2- yl]thiomethyl-3-cephem-4-carboxylate

I-44 : 7-[(Z)-2-(2-aminothiazol-4-yl)-2-(2-carboxyprop-2-oxyimino)

acetamido]-3-[4,6-diamino-1-(4-chlorophenyl)-pyrimidinium-2-yl] thiomethyl-3-cephem-4-carboxylate

I - 45 : 7-[(Z)-2-(2-aminothiazol-4-yl)-2-(l-carboxyeth-1-oxyimino)

acetamido]-3-[4,6-diamino-1-propylpyrimidinium-2-yl]thiomethyl-3- cephem-4-carboxylate

I - 46 : 7-[ (Z)-2-(2-aainothiazol-4-yl)-2-(2-propyn-1-oxyimino)acetamido]- 3-(4,6-diamino-1-methylpyrimidinium-2-yl)thiomethyl-3-cephem-4- carboxylate

I - 47 : 7-[ (Z)-2-(2-aminot iazol-4-yl)-2-(2-propyn-1-oxyimino)acetamido}

-3-(4,6-diamino-l-ethylpyrimidinium-2-yl)thiomethyl-3-cephem-4- carboxylate

I-48 : 7-[(Z)-2-(2-aminothiazol-4-yl)-2-(2-carboxyprop-2-oxyimino) acetamido]-3-(1-cyclopropyl-4,6-diaminopyrimidinium-2-yl)-3- cephem-4-carboxylate

I - 49 : 7-[ (Z)-2-(2-aminothiazol-4-yl)-2-(2-propen-1-oxyiaino)acetamido] -3-(4,6-diamino-1-methylpyrimidiniun-2-yl)-3-cephen-4-carboxylate

I - 50 : 7-[ (Z)-2-(2-aιinothiazol-4-yl)-2-(2-propen-1-oxyimino)acetamido]- 3-(4,6-diamino-1-ethylpyrimidinium-2-yl)-3-cephem-4-carboxylate

Comparative compound : Ceftazidime

In-vivo absorbency of the invented compounds( I ) was studied in SD rat(S) weighing 220~340g, as follows : The test compound was intravenously administered in a dose of 20mg/kf respectively to 2~5 rats. The blood samples from the femoral vein of the rats were taken every hour after administration, and analyzed by bio-assay(agar well method). The results were shown in Table 3.

The present invention is described in detail by the following Preparations and Examples :

Preparation 1 : Preparation of 4,6-diamino-1-methyl-2(1H)-pyrimidinethione

Sodium metal (4.6g) was added to dried ethyl alcohol (100mℓ), and refluxed for an hour. After N-methylthiourea (9g) and malononitrile

(6.6g) were added thereto, the reaction mixture was refluxed for 24 hours.

The reaction mixture was cooled to room temperature and neutralized with cone. hydrochloric acid. The precipitates were filtered, washed with water (20mℓ) and ethyl alcohol (50mℓ) and dried in vacuo to give the above-indicated compound (8.1g) in pale yellow solid.

m.P. : 185ºC~(decomp.)

NMR : δ (D₂O + acetone-d₅)

3.80(s, 3H), 5.39(s, 1H),

MS(EI) : 156(M⁺), 126

IR(KCl , cm^-1 ) : 3441 , 3335(N-H) , 1682 ( C=N) , 1095(C=S)

Preparation 2 : Preparation of 4,6-diamino-1-ethyl-2(1H)-pyrimidinethione

Sodium metal (4.6g) was added to dried ethyl alcohol (100mℓ), and refluxed for an hour. After N-ethylthiourea (10.4g) and malononitrile (6.6g) were added thereto, the obtained reaction mixture was refluxed for 48 hours. The reaction mixture was cooled to room temperature and neutralized with cone, hydrochloric acid. The precipitates were filtered, washed with ethyl alcohol (50mℓ), and the filtrate was concentrated under reduced pressure. The residue was chromatographed over silica gel to give the above-indicated compound (6.2g) in yellow solid.

m.p. : 197ºC~(decomp.)

NHR : δ (D₂O + acetone-d₅)

1.32(t, 3H), 4.61(q, 2H), 5.68(s, 1H)

MS(EI) : 170(M⁺), 142

IR(KCl. cm^-1) : 3480, 3200(N-H), 1665(C=N), 1130(C=S)

Preparation 3 : Preparation of 4,6-diamino-1-propyl-2(1H)-pyrimidinethione

Sodium metal (4.6g) was added to dried ethyl alcohol (100mℓ), and refluxed for an hour. After N-propylthiourea (11.8g) and malononitrile (6.6g) were added thereto, the reaction mixture was refluxed for 72 hours, cooled to room temperature, and neutralized with cone. hydrochloric acid. The precipitates were filtered, washed with ethyl alcohol (50mℓ), and the filtrate was concentrated under reduced pressure. The residue was chromatographed over silica gel to give the above-indicated compound (5.7g) in yellowish brown solid.

m.p. : 195ºC~(decomp.)

NMR : δ (D₂O + acetone-d₅)

0.96(t, 3H), 1.81(m, 2H), 4.51(t, 2H), 5.46(s, 1H)

MS(EI) : 184(H⁺), 142

IR(KCl, cm^-1) : 3310, 3200(N-H), 1634(C=N), 1150(C=S) Preparation 4 : Preparation of 1-butyl-4,6-diamino-2(1H)-pyrimidinethione

Sodium metal (4.6g) was added to dried ethyl alcohol (100mℓ), and refluxed for an hour. After N-butylthiourea (13.2g) and malononitrile (6.6g) were added thereto, the reaction mixture was refluxed for 72 hours, cooled to room temperature and neutralized with cone, hydrochloric acid. The precipitates were filtered, washed with ethyl alcohol (50mℓ), and the filtrate was concentrated under reduced pressure. The residue was chromatographed over silica gel to give the above-indicated compound (4.6g) in brown solid.

m.p. : 195ºC~(decomp.)

NMR : δ (D₂O + acetone-d3)

0.88(t, 3H), 1.36(m, 2H) , 1.69(m, 2H), 4.59(t, 2H), 5.41(s, 1H)

MS(EI) : 198(M+), 142

IR(KCl, cm^-1) : 3320, 3200(N-H), 1640 (C=N), 1110(C=S)

Preparation 5 : Preparation of 1-allyl-4,6-diamino-2(1H)-pyrimidinethione

Sodium metal (4.6g) was added to dried ethyl alcohol (100mℓ), and refluxed for an hour. After N-allylthiourea (11.6g) and malononitrile (6.6g) were added thereto, the reaction mixture was refluxed for 72 hours, cooled to room temperature and neutralized with cone. hydrochloric acid. The precipitates were filtered, washed with ethyl alcohol (50mℓ) , and the filtrate was concentrated under reduced pressure. The residue was chromatographed over silica gel to give the above-indicated compound (6.2g) in yellowish brown solid.

m.p. : 193ºC~(decomp.)

NMR : δ (CD₃OD)

5.42(s, 1H), 5.16~6.11(m, 5H)

MS(EI) : 182(M+), 142 IR(KCl , cm ^{- 1}) : 3310, 3260 (N-H) , 1645 (C=N) , 1012 (C=S)

Preparation 6 : Preparation of 1.4,6-triamino-2(1H)-pyrimidinethione Sodium metal (4.6g) was added to dried ethyl alcohol (100mℓ), and refluxed by heating for an hour. After malononitrile (6.6g) and thiosemicarbazide(9.1g) were added thereto, the reaction mixture was refluxed for 24 hours, cooled to room temperature. The precipitates were filtered, washed with ethyl alcohol (50mℓ), and dried under reduced pressure to give the above-indicated compound (8.3g) in white solid.

m.p. : 225ºC~(decomp.)

NMR : δ (D₂O + acetone-d₅)

5.42(s, 1H)

MS(EI) : 157(M⁺), 126

IR(KCl , cm ^{- 1}) : 3440, 3420(N-NH₂) , 3310, 3260(N-H) , 1645(C=N) , 1138(C=S)

Preparation 7 : Preparation of 4,6-diamino-1,5-dimethyl-2(1H)- pyrimidinethione

A. Preparation of methyl (±)-2-cyanopropionate

To (±)-2-bromopropionic acid (81.08g) was added water (70mℓ).

Sodium carbonate (28.62g) was added slowly over an hour and dissolved therein. A solution of potassium cyanide(37.77g) dissolved in water (75mℓ) was addded, and heated to about 50ºC. Accordingly as the reaction progressed, the temperature of the reaction solution rose to 90ºC. The reaction solution was stirred at 90 a 100ºC for an hour, cooled to room temperature, and neutralized with cone, hydrochloric acid (60mℓ). Afterwards, the thus neutralized solution was concentrated under reduced pressure, ethyl alcohol(300mℓ) was added to the concentrated solution. The ethanolic solution was concentrated under reduced pressure again. To the residue was added ethyl alcohol (700mℓ), followed by filtration. After cone, sulfuric acid(l~5mℓ) was added to the filtrate, the solution was refluxed for 5 hours and distilled to remove about 300mℓ of ethylalcohol. The solution was concentrated under reduced pressure, and residue was added to sodium carbonate saturated solution (200mℓ). After extraction with ether(400mℓ), the separated organic layer was washed with a 10% saline solution (500mℓ) and a saturated saline solution (200mℓ), and dried over anhydrous magnesium sulfate, filtered and then concentrated. The residue was distilled under reduced pressure to give the colorless above-indicated compound(44.74g).

Yield : 70%

b.P. : 87~90ºC/12 torr

HUE : δ (CDCl₃)

1.33(t, 3H), 1.60(d, 3H) , 3.55(q, 1H), 4.28(q, 2H).

B. Preparation of (±)-2-cyanopropionamide

To ethyl (±)-2-cyanopropionate (44.74g) was added cone, aqueous ammonia solution (200mℓ). The reaction mixture was stirred at room temperature for an hour and concentrated under reduced pressure. After addition of ethyl alcohol (200mℓ) , the ethanolic solution was concentrated again. The residue was dried in a vacuum oven to give the green above-indicated compound (33.00g). Yield : 96%

NMR : δ (DHSO-d₅)

1.40(d, 3H) , 3.74(q, 1H) , 7.39(bs, 1H) , 7.82(bs, 1H) . C. Preparation of 2-methylmalononitrile

(±)-2-Cyanopropionamide (33.00g), and phosphorus pentachloride (28.07g) ground minutely in a mortar were added to a flask equipped with a distillation apparatus. While producing a vaccum using a water pump, the mixture was stirred at 90~100ºC for 20 minutes to remove hydrogen chloride gas and phosphorus oxychloride, and distilled under reduced pressure in a bath heated to 180ºC to give the above-indicated compound(15.67g). This compound was solidified to a white solid state at room temperature.

Yield : 58%

b.p. : 86~89ºC/12torr

NNR : δ (DHSO-d₅)

1.63(d, 3H), 4.76(q, 1H) D. Preparation of 4.6-diamino-1,5-dimethyl-2(1H)-pyrimidinethione

After sodium metal (9.01g) was dissolved in dried ethyl alcohol (150mℓ) under nitrogen stream, N-methylthiourea(17.67g) was added thereto and refluxed for an hour. 2-Hethylmalononitrile (17.67g) was added to the solution and then refluxed for 15 hours. The reaction mixture was cooled to 40ºC and filtered. The filtered solid was washed with cold ethyl alcohol (100mℓ) and dried to give the pale yellow above- indicated compound(25.20g).

m.p. : 230ºC~(decomp.) Yield : 76%

TLC : Rf 0.2(MeOH/CH₂Cl₂ = 1/5)

NMR : δ (DMSO-d₅)

1.6(s, 1H), 3.60(s, 3H), 4.92(bs, 4H)

MS(EI) : 170(M⁺), 156

IR(KC], cm^-1) : 3480, 3360(N-H), 1623(C=N), 1090(C=S)

Preparation 8 : Preparation of 4,6-diamino-1-ethyl-5-methyl-2(1H)- pyrimidinethione

After Sodium metal (2.30g) was dissolved in dried ethyl alcohol

(50mℓ), N-ethylthiourea (5.20g) was added and refluxed for an hour.

2-Methylmalononitrile (4.0g) was added to the solution and then refluxed for 15 hours. The reaction mixture was cooled to room temperature, neutralized with cone, hydrochloric acid, and filtered. After water

(20mℓ) was added to the filtered solid, the mixture was stirred for 10 minutes, and filtered. The filtered solid was dried to give the pale yellow above-indicated compound(3.57g).

m.p. : 281ºC~(decomp.)

Yield : 39%

NMR : δ (DMSO-d₅)

1.15(t, 3H), 1.75(s, 3H), 4.57(bs, 2H), 6.24(bs, 2H), 6.68(bs, 2H),

MS(EI) : 184(M⁺), 156

IR(KCl, cm^-1) : 3418, 3300(N-H), 1620(C=N), 1105(C=S) Preparation 9 : Preparation of 5-methyl-1,4,6-triamino-2(1H)- pyrimidinethione

After sodium metal (2.30g) was dissolved in dried ethyl alcohol (50mℓ), thiosemicarbazide (4.55g) was added thereto and refluxed for an hour. 2-Methylιalononitrile (4.0g) was added to the mixture and then refluxed for 15 hours. The reaction mixture was cooled to

40ºC, and filtered, washed with ethyl alcohol (50mℓ.), and dried to give the pale yellow above-indicated compound(3.78g).

m.p. : 215°C~(decomp.)

Yield : 44%

NNMR : δ (DHSO-d₅)

1.68(s, 3H), 3.48(bs, 2H), 5.20(bs, 2H), 5.95(bs, 2H),

MS(EI) : 171(M⁺), 156

IR(KCl, cm^-1) : 3470, 3340(N-H), 1622(C=N), 1060(C=S)

Preparation 10 : Preparation of 4,6-diamino-5-ethyl-1-methyl-2(1H)- pyrimidinethione A. Preparation of methyl (±)-2-cyanobutyrate

To (±)-2-bromobutyric acid(167.01g) was added water(150mℓ). Sodium carbonate (54.05g) was added slowly over an hour and dissolved therein. A solution of potassium cyanide (68.55g) dissolved in water (150mℓ) was added, and heated to about 50ºC. Accordingly as the reaction progressed, the temperature of the reaction solution rose to 80ºC. The reaction solution was stirred at 80~90°C for an hour, cooled to room temperature, and neutralized with cone. hydrochloric acid (120mℓ). Afterwards, the thus neutralized solution was concentrated under reduced pressure, and ethyl alcohol (500mℓ) was added to the residue. The obtained ethanolic solution was concentrated under reduced pressure again. To the residue was added ethyl alcohol (700mℓ), followed by filtration. After cone, sulfuric acid (3mℓ) was added to the filtrate, the solution was refluxed for 5 hours and distilled to remove about 300mℓ of ethyl alcohol. The solution was concentrated under reduced prrssure, and the residue was added to sodium carbonate saturated solution(400mℓ) . After extraction with ether (500mℓ), the separated organic layer was washed with a 10% saline solution (500mℓ) and a saturated saline solution(300mℓ), dried over anhydrous magnesium sulfate, filtered and then concentrated. The residue solution was distilled under reduced pressure to give the colorless above-indicated compound(49.90g).

Yield : 35%

b .p. : 93~ 96-C/12torr

NMR : δ (CDCl₃)

1.14 (t, 3H) , 1.34 (t, 3H) , 2.01 (m, 2H) , 3.47(t, 1H) , 4.28(q, 2H) B. Preparation of (±)-2-cyanobutyramide

To ethyl (±)-2-cyanobutyrate (49.90g) was added ethyl alcohol (40mℓ). After cone, aqueous ammonia solution(200mℓ) was added thereto over 10 minutes, the solution was stirred at 30~40ºC for 30 minutes. Ether(500mℓ) was added to the solution and stirred for 10 minutes.

The precipitates were filtered, and dried to give the colorless above-indicated compound(31.96g).

Yield : 81% NMR : δ (DMSO-d₅)

0.98(t, 3H), 1.83(m, 2H), 3.63(t, 1H), 7.43(bs, 1H), 7.76(bs, 1H)

L Preparation of 2-ethylnalononitrile

(±)-2-Cyanobutyramide (31.96g), and phosphorus pentachloride (23.85g) ground in a mortar were added to a flask equipped with a distillation apparatus. While producing a vaecum using a water pump, the mixture was stirred at 90~100ºC for 20 minutes to remove hydrogen chloride gas and phosphorus oxychloride, and distilled under reduced pressure in a bath heated to 180ºC to give the above-indicated compound (19.45g).

Yield : 73%

NME : δ (DHSO-d₅)

1.26(t, 3H), 2.10(m, 2H), 3.73(t, 1H)

D. Preparation of 4.6-diamino-5-ethyl-l-methyl-2(lH)-pyrimidinethione

After sodium metal (2.30g) was dissolved in dried ethyl alcohol (50mℓ), N-methylthiourea(4.50g) was added thereto and refluxed for an hour. 2-Ethylmalononitrile (4.70g) was added to the solution and then refluxed for 18 hours. The reaction mixture was cooled to 40ºC, neutralized with cone, hydrochloric acid, and filtered. To the filtered solid was added water(50mℓ). The mixture was stirred for 10 minutes, filtered, and dried to give the white above-indicated compound (4.15g).

m.p. : 259ºC~ (decomp.)

Yield : 45%

NMR : δ (DMSO-d₅) 0.92(t, 3H) , 2.34(q, 2H) , 3.82(s, 3H) , 6.78(bs, 211) . 7.06(bs, 2H) MS (EI) : 184 (M⁺) , 169 , 156

IR(KCl . cm'¹) : 3410 , 3280 (N-H) , 1645 (C=N) , 1086(C=S) Preparation 11 : Preparation of 4,6-diamino-1,5-diethyl-2(1H)- pyrimidinethione

After sodium metal (2.30g) was dissolved in dried ethyl alcohol (50mℓ), N-ethylthiourea (5.20g) was added thereto and refluxed for an hour. 2-Ethylmalononitrile (4.70g) was added to the reflux mixture and then refluxed for 18 hours. The reaction mixture was cooled to 40ºC, and adjusted pH to 5 with a 28% solution of hydrogen chloride dissolved in isopropyl alcohol. The reaction mixture was filtered, and then water(50mℓ) was added to the filtered solid. After the solution was stirred for 10 minutes and filtered again, the residue was dried to give the pale yellow above-indicated compound(2.79g). m.p. : 269ºC~(decomp.)

Yield. : 28%

NϋE : δ (DMSO-d₅)

0.91(t, 3H), 1.16(t, 3H),2.28(q, 2H), 4.57(bs, 2H), 6.45(bs, 2H).

6.70(bs, 2H)

MS(EI) : 198(M⁺), 170

IR(KCl, cm^-1) : 3380, 3320(N-H), 1646(C=N), 1101(C=S) Preparation 12 : Preparation of 4,6-diamino-1-phenyl-2(1H)- pyrimidinethione

Sodium metal (6.6g) was added to dried ethyl alcohol(100mℓ), and refluxed for an hour. After N-phenylthiourea (9g) and malononitrile (6.6g) were added thereto, the reaction mixture was refluxed for 72 hours. The reaction mixture was cooled to room temperature and neutralized with cone, hydrochloric acid. The precipitates were filtered, washed with water(20mℓ) and ethyl alcohol (50mℓ), and dried in vacuo to give the above-indicated compound (4.7g) in a pale yellow color.

m.p. : 281ºC~(decomp.)

NMR : δ (acetone-dβ)

5.48(s, 1H), 5.90(bs, 2H), 6.52(bs, 2H). 6.80~7.70(m, 5H)

MS(EI) : 218(M⁺)

IR(KC1. cm-¹⁾ : 3484, 3400(N-H), 1630(C=N), 1182(C=S)

Preparation 13 : Preparation of 1-(4-chlorophenyl)-4,6-diamino-2(1H)- pyrimidinethione N-(4-Chlorophenyl)-thiourea (llg) and malononitrile (θ.6g) were reacted in the same method as described in Preparation 12 to give the above-indicated compound (5.3g).

m.p. : 275ºC~(decomp.)

KME : δ (DMSO-d₅)

5.31(s, 1H). 6.38(bs. 2H), 6.87(bs, 2H), 7.18(d, 2H), 7.55(d, 1H)

MS(EI) : 252(H⁺)

IR(KCl. cm^-1) : 3460, 3400(N-H), 1630(C=N), 1095(C=S) Preparation 14 : Preparation of 4,6-diamino-1-(2,4-dimethylphenyl)-2(1H)- pyrimidinethione

N-(2,4-Dimethylphenyl)-thiourea (10.8g) and malononitrile (6.6g) were reacted in the same method as described in Preparation 12 to give the above-indicated compound (5.7g).

m.p. : 212ºC~(decomp.)

NMR : δ (acetone-d₅)

2.08(s, 3H), 2.30(s, 3H), 5.58(s, 1H), 5.91(bs, 2H), 6.80~7.20 (m, 5H)

MS(EI) : 246(M⁺)

IR(KCl. cm^-1) : 3440, 3300(N-H), 1632(C=N). 1090(C=S)

Preparation 15 : Preparationof4,6-diamino-1-(2,6-dimethoxyphenyl)- 2(1H)-pyrimidinethione

N-(2,6-Dimethoxyρhenyl)-thiourea (11.5g) and malononitrile (6.6g) were reacted in the same method as described in Preparation 12 to give the above-indicated compound (6.2g).

m.p. : 207ºC~ (decomp.)

NHR : δ (acetone-d₅)

3.64(s, 6H), 5.44(s, 1H), 5.89(bs, 2H), 6.48(bs, 2H), 6.40~7.01 (a, 3H)

HS(ED : 278(M⁺)

IR(KCl. cm^-1) : 3438, 3310(N-H), 1631(C=N). 1043(C=S) Preparation 16 : Preparation of 4,6-diamino-1-(4-hydroxyphenyl)-2(1H}- pyrimidinethione

N-(4-hydroxyphenyl)-thiourea (9.3g) and malononitrile (6.6g) were reacted in the same method as described in Preparation 12 to give the above-indicated compound (4.1g).

m.p. : 282ºC~

NMR : δ (DMSO-d₅)

5.30(s, 1H), 6.19(bs, 2H). 6.76(bs, 2H), 6.84(s, 4H), 9.78(bs, 1H) MS(EI) : 234(H⁺)

IR(KC]. cm-) : 3480, 3470(N-H), 1640(C=N), 1038(C=S)

Preparation 17 : Preparation of 1-cyclopropyl-4,6-diamino-2(1H)- pyrimidinethione

N-cyclopropylthiourea (6.2g) and malononitrile(6.6g) were reacted in the same method as described in Preparation 12 to give the pale yellow above-indicated compound(3.7g) .

m,P. : 242ºC~ (decomp. )

NMR : δ (DMSO-d₅)

0.88~1.52(m, 4H), 2.80~3.16(m, 1H), 5.48(s, 1H)

MS(EI) : 182(M⁺)

IR(KCl. cm^-1) : 1580(C=N), 1015(C=S) Preparation 18 : Preparation of 3-acethoxymethyl-7-[(Z)-2-(2- aminothiazol-4-yl)-2-(methoxyimino)acetamido]-3- cephem-4-carboxylic acid A. Preparation of ethyl (Z)-2-(methoxyimino)-2-[2-(triphenylmethyl) aminothiazol-4-yl]acetate

To ethyl (Z)-2-(hydroxyimino)-2-[2-(triphenylmethyl)aminothiazol-4-yl] acetate(46g) were added iodo methane(28.4g), potassium carbonate (27.6g) and dimethylsulfoxide(500mℓ), and the mixture was stirred for 5 hours at room temperature. After ethyl ether(2ℓ) was added to the reaction mixture, the mixture was washed 5 times with distilled water(500mℓ). The separated organic layer was dehydrated with anhydrous magnesium sulfate, filtered, and then concentrated. The residue was chromatographed over silica gel to give the above-indicated compound (35.2g) as a pale yellow solid.

B. Preparation of (Z)-2-(methoxyimino)-2-[2-(triphenylmethyl)

aminothiazol-4-yl]acetic acid

After the compound(23.6g) prepared in (A) was dissolved in a mixed solvent of ethyl alcohol(100mℓ) and tetrahydrofuran(50mℓ), aqueous 5N-sodium hydroxide solution (20mℓ) was added thereto. The reaction mixture was stirred for 2 hours and neutralized with 5N-hydrochrolic acid (20mℓ). After the organic solvent was removed under reduced pressure, ethyl acetate (1 ℓ) was added to the residue, and then the reaction mixture was washed twice with distilled water(500mℓ).

The separated organic layer was dehydrated, and concentrated to give the above-indicated compound(20.7g) as a white solid. C. Preparation of 3-acethoxymethyl-7-[(Z)-2-(2-aminothiazol-4-yl)-2-

(methoxyimino)acetamidol-3-cephem-4-carboxylic acid

The compound(4.4g) prepared in (B) was dissolved in N,N-dimethyl acetamide(30mℓ). To the solution were added triethylamine (3.5mβ) and mesithylene sulfonyl chloride(2.3g) at 0ºC, and stirred for 20 minutes. After adding 7-aminocephalosporanic acid (2.9g), the reaction mixture was stirred again for 2 hours. To the mixture was added ethyl acetate (300mℓ), and it was washed with 1%-hydrochloric acid (100mℓ), sodium chloride solution(lθθmℓ) and distilled water(200mℓ). The separated organic layer was dehydrated, and concentrated. Formic acid (40mℓ) was added to the residue. After the solution was stirred for 2 hours at room temperature, the recipitates were filtered off.

The filtrate was concentrated under reduced pressure, triturated with ethyl ether(100mℓ). The solid was filtered, washed, and dried to give the above-indicated compound(4, 17g) as a pale yellow solid.

NMR : δ (D₂O + NaHCO₃)

2.08(s, 3H), 3.52(ABq, 2H) , 3.99(s, 311), 4.41(ABq, 2H) , 5.23 (d, 1H), 5.84(d, 1H), 7.01(s, 1H) Preparation 19 : Preparation of 3-acethoxymethyl-7-[(Z)-2-(2-aminothiazol- 4-yl)-2-(ethoxyimino)acetamido]-3-cephem-4-carboxylic acid

A. Preparation of ethyl (Z)-2-(ethoxyimino)-2-[2-(triphenylmethyl)

aminothiazol-4-yl]acetate

To ethyl (Z)-2-(hydroxyimino)-2-[2-(triphenylmethyl)aminothiazol-4-yl] acetate(46g) were added bromoethane(21.8g), potassium carbonate (27.6g) and dimethylsulfoxide(500mℓ), and the solution was stirred for 7 hours at room temperature. After ethyl ether (2.2 ) was added thereto, the mixture was washed 5 times with distilled water (500mℓ).

The separated organic layer was dehydrated, and concentrated to give the above-indicated compound(41.4g) as a pale yellow solid.

B. Preparation of (Z)-2-(ethoxyimino)-2-[2-(triphenylmethyl)

aminothiazol-4-yl]acetic acid

The compound (24.3g) prepared in (A) was dissolved in a mixed solvent of ethyl alcohol(100mℓ) and tetrahydrofuran (50mℓ). After aqueous 5N-sodium hydroxide solution(20mℓ) was added thereto, the reaction mixture was stirred for 2 hours at room temperature. The reaction mixture was neutralized with 5N-hydrochloric acid, and the organic solvent was removed under reduced pressure. To the residue was added ethyl acetate(1ℓ), and it was washed twice with distilled water(500mfl). The separated organic layer was dehydrated, and concentrated to give the above-indicated compound(19.8g) in white solid.

C. Preparation of 3-acethoxymethyl-7-[(Z)-2-(2-aminothiazol-4-yl)- 2-(ethoxyimino)acetamido]-3-cephem-4-carboxylic acid

(Z)-2-(ethoxyimino)-2-[2-(triphenylmethyl)aminothiazol-4-yl] acetic acid (4.6g) was reacted in the same method as described in (C) of Preparation 18 to give the above-indicated compound(3.98g) in white solid. NJE : δ (D₂O + NaHCO₃)

1.31(t, 3H), 2.02(s, 3H), 3.57(ABq, 2H) , 4.07(q, 2H) , 4.52(ABq, 2H),

5.20(d, 1H), 5.81(d, 1H), 7.00(s, 1H) Preparation 20 : Preparation of 3-acethoxymethyl-7-[(Z)-2-(2-aminothiazol- 4-yl)-2-(2-carboxyprop-2-oxyimino)acetamido]-3-cephem-4- carboxylic acid dihydrochloride A. Preparation of ethyl (Z)-2-(2-tert-butoxycarbonylprop-2-oxyimino)

-2-[2-(triphenylmethyl)aminothiazol-4-yl]acetate

To ethyl (Z)-2-{hydroxyimino)-2-[2-(triphenylmethyl)aminothiazol-4-yl]acetate(46g) were added potassium carbonate(27.6g), tert-butyl-2-bromo- 2-methylpropionate(24.1g) and dimethylsulfoxide(300mℓ), and then the solution was stirred for 6 hours at room temperature. Afterwards, distilled water (100mℓ) was added therein, the solution was stirred again for an hour. The precipitates were filtered, washed with distilled water(500mℓ), and dried under reduced pressure to give the above-indicated compound(45.1g) as a white solid.

B. Preparation of (Z)-2-(2-tert-butoxycarbonylprop-2-oxyimino)-2-[2- (triphenylmethyl)aminothiazol-4-yI]acetic acid

The compound(30g) prepared in (A) was reacted in the same method as described in (B) of Preparation 19. The resultant solid was recrystalized with methyl alcohol(100mℓ) to give the above-indicated compound(21g) as a white solid.

C. Preparation of 3-acethoxymethyl-7-[(Z)-2-(2-aminothiazol-4-yl)-2- (2-carboxyprop-2-oxyimino)acetamido-3-cephem-4-carboxylic acid dihydrochloride

(Z)-2-(2-tert-butoxycarbonylprop-2-oxyimino)-2-[2-(triphenylmethyl) aminothiazol-4-yl]acetic acid (5.7g) was dissolved in N,N-dimethylformamide (30mℓ). Triethylamine (3.5mℓ) and mesithylenesulfonyl chloride(2.3g) were added thereto at to 0ºC, and the obtained solution was stirred for 10 minutes. After 7-aminocephalosporanic acid (2.9g) was added to the solution, the mixture was further stirred for 2 hours.

To the reaction mixture was added ethyl acetate(300mℓ), and it was then washed with 1%-hydrochloric acid (100mℓ), saline solution (100mℓ), and distilled water (200mℓ) . The separated organic layer was dehydrated, and concentrated. To the residue were added formic acid (40mℓ) and cone, hydrochloric acid(3mℓ) at 0ºC. After stirring for 2 hours, the solid was filtered off. The filtrate was concentrated under reduced pressure, and triturated with ethyl ether. The solid was filtered, washed, and dried to give the above-indicated compound (3.87g) in a yellow solid.

NMR : δ (Acetone-d₅)

1.50(s, 6H), 2.05(s, 3H), 3.53(ABq, 2H), 4.38(ABq, 2H) , 5.12(d, 1H),

5.98(q, 1H), 7.05(s, 1H), 7.32(bs, 2H).

Preparation 21 : Preparation of 3-acethoxymethyl-7-[(Z)-2-(2-aminothiazol- 4-yl)-2-(1-carboxyeth-1-oxyimino)acetamido]-3-cephem- 4-carboxylic acid

A. Preparation of ethyl (Z)-2-(1-tert-butoxycarbonyleth-1-oxyimino)-

2-[2-(triphenylmethyI)aminothiazol-4-ynacetate

After potassium carbonate (27.6g), tert-butyl-2-bromopiopyonate (23g) and dimethylsulfoxide(300mℓ) were added to ethyl (Z)-2- (hydroxyimino)-2-[2-(triphenylmethyl)aminothiazol-4-yl]acetate(46g), the mixture was stirred for 5 hours at room temperature. Ethyl ether (2ℓ ) was added thereto, and the mixture washed 5 times with distilled water(500mℓ). The separated organic layer was dehydrated, and concentrated to give the above-indicated compound (51g) in a pale yellow solid,

B. Preparation of (Z)-2-(1-carboxyeth-1-oxyimino-2-[2-(triphenylmethyl) aminothiazol-4-yl]acetic acid

The compound(27.9g) prepared in (A) was dissolved in a mixed solvent of ethyl alcohol(100mℓ) and tetrahydrofuran(50mℓ). Afterwards, a 5N-sodium hydroxide aqueous solution (40mℓ) was added thereto, and the solution was stirred for 2 hours at room temperature. The reaction mixture was neutralized with 5N-hydroehioric acid (40mℓ) , and the organic solvent was removed under reduced pressure. To the residue was added ethyl acetate(1ℓ), and it was washed twice with distilled water (500mℓ). The separated organic layer was dehydrated and dried to give the above-indicated compound(23.1g) in a pale yellow solid.

C. Preparation of 3-acethoxymethyl-7-[(Z)-2-(2-aminothiazol-4-yl)- 2-(1-carboxyeth-1-oxyimino)acetamido)-3-cephem-4-carboxylic

acid

To a solution of (Z)-2-(1-carboxyeth-1-oxyimino)-2-[2-(triphenyl methyl)aminothiazol-4-yl]acetic acid(5.6g) dissolved in N.N-dimethyl acetamide(30mℓ) were added triethylamine (1.4mℓ) and mesithylene sulfonylchloride (2.3g) at -10ºC. After stirred for 50 minutes, triethylamine(2.8mℓ) and 7-aminocephalosporanic acid (2.9g) was added thereto. The reaction mixture was stirred again for 2 hours.

After raising the temperature of the reaction mixture to roon temperature, ethyl acetate (500mℓ) was added thereto. The reaction mixture was washed twice with 1% hydrochloric acid (200mℓ), saline solution (200mℓ) and distilled water (200mℓ). The separated organic layer was dehydrated, and concentrated. To the residue was added formic acid (50mℓ). The solution was stirred for 2 hours, and the obtained solid was filtered off. The filtrate was concentrated udnder reduced pressure, and powder-solidified by addition of ethyl ether. The solid was filtered, washed, and dried to give the above-indicated compound (3.65g).

NJE : δ (D₂O + NaHCO₃)

1.45(d, 3H), 2.07(s. 3H), 3.54(ABq, 2H), 4.64(q, 1H), 4.91(ABq,

2H), 5.24(d, 1H), 5.86(dd, 1H), 7.03(s, 1H)

Preparation 22 : Preparation of 3-acethoxymethyl-7-[(Z)-2-(2-aminothiazol- 4-yl)-2-(1-carboxymethyoxyimino)acetamido]-3-cephem-4 carboxylic acid

A. Preparation of ethyl (Z)-2-(butoxycarbonylmethoxyimino)-2-[2- (triphenylmethyl)aminothiazol-4-yl]acetate

To ethyl (Z)-2-(hydroxyimino)-2-[2-(triphenylmethyl)aminothiazol-4-yl]acetate(46g) were added potassium carbonate(27.6g), tert-butyl-2- bromopropionate(20g) and dimethylsulfoxide(300mℓ). The reaction mixture was stirred for 5 hours at room temperature, followed by addition of ethyl ether (2ℓ). After the reaction mixture was washed 5 times with distilled water(500mℓ), the separated organic layer was dehydrated and concentrated to give the above-indicated compound(47.2g) in a yellow solid. B. Preparation of (Z)-2-(carboxymethoxyimino)-2-[2-(triphenylmethyl) aminothiazol-4-yl]acetate

The compound(27.2g) prepared in (A) was reacted in the same method as described in (B) of Preparation 21 to give the above-indicated compound (21.3g) in a pale yellow solid.

C. Preparation of 3-acethoxymethyl-7-[(Z)-2-(2-aminothiazol-4-yl)-2- (1-carboxymethoxy-1-oxylmino)acetamido]-3-cephem-4-carboxylic acid

To a solution of (Z)-2-(1-carboxymethoxy-1-oxyimino)-2-[2-(triphenylmethyl)aminothiazol-4-yl]acetic acid (5.4g) dissolved in N.N-dimethylacetamide (30mℓ) were added triethylamine (1.4mℓ) and mesithylene sulfonyl chloride (2.3g) at -20ºC. After stirring for an hour, triethylamine (2.8mℓ) and 7-aminocephalosporanic acid (2.9g) were added thereto. The solution was stirred again for 2 hours. After slowly raising the temperature of the reaction mixture to room temperature, ethyl acetate (500mℓ) was added thereto. The reaction mixture was washed twice with 1% hydrochloric acid(200mℓ), saline solution(200mℓ) and distilled water (200mℓ). The separated organic layer was dehydrated, and concentrated. To the residue was added formic acid (50mℓ). The solution was stirred for 2 hours at room temperature and the formed solid was filtered off. The filtrate was concentrated under reduced pressure, and then triturated with ethyl ether. The solid was filtered, washed, and dried to give the above-indicated compound (3.32g) in a yellow solid.

NHR : δ (D₂O + NaHCO₃)

2.06(s, 3H), 3.52(ABq, 2H), 4.73(ABq, 2H), 4.82(s, 2H), 5.21

(d, 1H), 5.84(d, 1H), 7.07(s, 1H) Preparation 23 : Preparation of 3-acethoxymethyl-7-[(Z)-2-(2- aminothiazol-4-yl)-2-(2-propen-1-oxyimino)acetamido]- 3-cephem-4-carboxylic acid

A. Preparation of ethyl (Z)-2-(2-propen-1-oxyimino)-2-[2- (triphenylmethyl)aminothiazol-4-yl]acetate

The above-indicated compound(39.Ig) was prepared in the same method as described in (A) of Preparation 19, except that 3-romopropyne(24.2g) was used in place of bromoethane.

B. Preparation of (Z)-2-(2-propen-1-oxyimino)-2-[2-(triphenylmethyl) aminothiazol-4-yl]acetic acid

The compound (24.9g) obtained in (A) was reacted in the same method as described in (B) of Preparation 18 to give the above-indicated compound (21. Ig).

C. Preparation of 3-acethoxymethyl-7-[(Z)-2-(2-aminothiazol-4- yl)-2-(2-propen-1-oxyimino)acetamido]-3-cephem-4-carboxylic acid

(Z)-2-(2-propen-1-oxyimino)-2-[2-(triphenylmethyl)aminothiazol-4-yl) acetic acid(4.7g) was reacted in the same method as described in (C) of Preparation 18 to give the above-indicated compound (4.05g) in a pale yellow solid.

NMR : δ (D₂O + NaHCO₃)

2.07(s, 3H), 3.52(ABq, 2H) , 4.81(s, 2H), 4.80(ABq, 2H),

5.23(d, 1H), 5.84(d, 1H), 5.15~6.24(m, 3H), 6.99(s, 1H) Preparation 24 : Preparation of 3-aeethoxymethyl-7-[(Z)-2-(2-aminothiazol-4-yl)-2-(2-propen-1-oxyimino)acetamido]-3-cephem- 4-carboxylic acid

A. Preparation of ethyl (Z)-2-(2-ρropyn-1-oxyimino)-2-[2- (triphenylmethyl)aminolthiazol-4-yl]acetate

The above-indicated compound(30.7g) was prepared in the same method as described in (A) of Preparation 19, except that 3-bromopropyne(14.9g) was used in place of bromoethane.

B. Preparation of (Z)-2-(2-propyn-1-oxyimino)-2-[2-(triphenylmethyl)

aminothiazol-4-ynacetic acid

The compound(24.8g) prepared in (A) was reacted in the same method as described in (B) of Preparation 19 to give the above-indicated compound (21.Ig).

C. Preparation of 3-acethoxymethyl-7-[(Z)-2-(2-aminothiazol-4-yl)- 2-(2-Propyn-1-oxyimino)acetamidol-3-cephem-4-carboxylic acid

(Z)-2-(2-propyn-1-oxyimino)-2-[2-(triphenylmethyl)aminothiazol-4-yl) acetic acid (4.7g) was reacted in the same method as described in (C) of

Preparation 17 to give the above-indicated compound(3.95g) in a yellow solid.

NMR : δ (D₂O + NaHCO₃)

2.06(s, 3H), 2.96(s, 1H), 3.56(ABq, 2H), 4.15(ABq, 211), 4.84

(s, 2H), 5.11(d, 1H), 5.84(d, 1H), 7.05(s, 1H) Preparation 25 : Preparation of 3-acethoxymethyl-7-[(Z)-2-(5-amino- 1,2,4-thiadiazol-4-yl)-2-(2-methoxyimino)acetamido]- 3-cephem-4-carboxylic acid A. Preparation of 2-(hydroxyimino)malononitrile

To a solution of malononitrile(66.1g) dissolved in water(50mℓ) and acetic acid(50mℓ), was added slowly sodium nitrite(69g) dissolved in water(lθθmℓ) at 4ºC, and then, stirred for 3 hours at room temperature. The reaction mixture was extracted 3 times with ethyl acetate (respectively, 500mℓ, 250mℓ and 250mℓ), dried with anhydrous magnesium sulfate, and concentrated in vacuo. The residue was triturated with ethyl ether to give the above-indicated compound (92.5g) in a white solid. B. Preparation of 2-(methoxyimino)malononitrile

To a solution of 2-(hydroxyimino)malononitrile (95g) dissolved in dimethylsulfoxide(200mℓ) were added potassium carbonate(140g) and dimethylsulfate(126.1g). The reaction mixture was stirred for an hour at room temperature and ethyl ether (700mℓ) was added thereto.

After the mixture was washed 5 times with distilled water (1ℓ), the separated organic layer was dehydrated, concentrated, and then, distilled under reduced pressure to give the above-indicated compound(90g) in a pale yellow liquid.

b .p. : 60~ 65ºC/20torr

NMR : δ (CDCl₃)

3.90 (s, 3H) . C. Preparation of 2-cyano-2-(methoxyimino)acetamidinium acetate

To a mixed solution of ammonium chloride(14.2g) dissolved in ethanol (90mℓ) and cone, ammonium hydroxide aqueous solution (178mℓ) was added 2-(methoxyimino)malononitrile(29g) at -5~0ºC, and the mixture was stirred for 10 hours at these temperatures. The reaction mixture was extracted 3 times with methylene chloride (respectively, 450mℓ 100mℓ and 100mℓ), dehydrated, filtered, and concentrated. The residue was dissolved in ethyl acetate, and crystalized with acetic acid to give the above-indicated compound (20.5g) in pale brown.

MR : δ (DMSO-d₅)

1.90(s, 3H), 1.90(s, 3H), 4.18(s, 3H), 7.88(s, 1H)

D. Preparation of 2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(methoxyimino) acetonitrile

To a solution of 2-cyano-2-(methoxyimino)acetamidinium acetate (12.5g) dissolved in methanol(100mℓ) was added triethylamine(23.4mℓ).

Thereafter, bromine (12.9g) was added slowly in small portions at -15ºC, and the mixture was stirred for 5 minutes at -15~-10ºC. Potassium thiocyanate(3.7g) dissolved in methanol(55mℓ) was then added dropwise to the mixture at temperatures of -10 to -5ºC, and the mixture was stirred for 2 hours at 0ºC. The reaction mixture was poured into ice water (1.2-5), and stirred for 30 minutes. The precipitates were filtered and dired to give the above-indicated compound (12.2g) in pale brown.

NMR : δ (DMSO-d₅)

3.90(s, 3H), 8.37(s, 2H). E. Preparation of 2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(methoxyimino) acetic acid

A solution of 2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(methoxyimino) acetonitrile(12.2g) dissolved in 4N- sodium hydroxide aqueous solution (250mℓ) was stirred for 5 hours at temperatures of 50 to 55°C. The reaction mixture was cooled to room temperature and the pH adjusted to 1 with phosphoric acid, followed by extraction with a 3 : 1 (v/v) mixed solvent of ethyl acetate and tetrahydrofuran. After the separated organic layer was dried, filtered and concentrated the residue was triturated with ethyl ether, and the solid was filtered to give the above-indicated compound(11.2g) in pale brown.

NMR : δ (DHSO-d₅)

3.91(s, 3H), 8.20(s, 2H). F. Preparation of 3-acethoxymethyl-7-[(Z)-2-(5-amino-1,2,4-thiadiazol- 3-yl)-2-(2-methoxyimino)acetamidol-3-cephem-4-carboxylic acid

2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(methoxyimino)acetic acid (2.0g) was dissolved in dried dimethylacetamide(20mℓ), and then cooled to -10ºC. Triethylamine(1.5mℓ) and mesithylene sulfonyl chloride(2.3g) was added therein, and the mixture was stirred for an hour at -10ºC. After addition of 7-amino-cephalosporanic acid(3.26g) and triethylamine (3mℓ), the mixture was stirred for 2 hours at room temperature. Water (100mℓ) was added to the reaction mixture. The mixture was adjusted pH to 1 with phosphoric acid, and extracted with a 3 : 1(v/v) mixed solvent of ethyl acetate and tetrahydrofuran. The reaction mixture was dried, filtered, and concentrated. The residue was triturated with isopropyl ether, and the solid was filtered to give the above-indicated compound(3.05g) in a clear brown solid.

NMR : δ (DMSO-d₅)

2.05(s, 3H). 3.2~3.6(ABq, 2H) , 3.95(s, 3H), 4.42~5.45(ABq,

2H), 5.18(d, 1H), 5.80(q, 1H), 8.20(s, 2H).

Preparation 26 : Preparation of 3-acethoxymethyl-7-[(Z)-2-(5-amino- 1,2,4,-thiadiazol-3-yl)-2-(2-carboxyprop-2-oxyimino) acetamido]-3-cephem-4-carboxylic acid A. Preparation of 2-(ethoxyiminp)malononitrile

2-(hydroxyimino)malononitrile (95g) and diethylsulfate (230mℓ) were reacted in the same method as described in (B) of Preparation 25 to give the above-indicated compound (97g) .

b.p. : 65~67ºC/13torr

NMR : δ (CDCl₃)

1.20(t, 3H), 4.20(q, 2H)

B. Preparation of 2-cyano-2-(ethoxyimino)acetamidinium acetate

2-(ethoxyimino)malononitrile (15.9g) was reacted in the same method as described in (C) of Preparation 25 to give the above-indicated compound (22.4g).

NMR : δ (DHSO-d₅)

1.20(t, 3H), 1.90(s, 3H), 4.10(q, 2H), 7.90(s, 4H). C. Preparation of 2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(ethoxyimino) acetonitrile

2-cyano-2-(ethoxyimino)acetamidinium acetate (13.1g) was reacted in the same method as described in (D) of Preparation 25 to give the above- indicated compound (12.1g).

HME : δ (DMSO-d₅)

1.37(t, 3H), 4.50 (q, 2H). 8.37 (s, 2H).

D. Preparation of 2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(ethoxyimino)

acetic acid

2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(ethoxyimino)acetonitrile (12.1g) was reacted in the same method as described in (E) of Preparation 25 to give the above-indicated compound (10.8g).

NMR : δ (DMSO-d₅)

1.20(t, 3H), 4.20(q, 2H), 8.21(s, 2H).

E. Preparation of 3-acethoxymethyl-7-[(Z)-2-(5-amino-1,2,4-thiadiazol- 3-yl)-2-(2-ethoxyimino)acetamido]-3-cephem-4-carboxylic acid

2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(ethoxyimino)acetic acid (2.14g) was reacted in the same method as described in (F) of Preparation 25 to give the above-indicated compound (3.31g).

NMR : δ (DMSO-d₅)

1.25(t, 3H), 2.05(s, 3H), 3.40~3.80(ABq, 2H), 4.22(q, 2H),

4.60~5.48(q, 1H), 8.28(s, 2H)

Preparation 27 : Preparation of 3-acethoxymethyl-7-[(Z)-2-(5-amino- 1,2,4-thiadiazol-3-yl)-2-(2-carboxyprop-2-oxyimino) acetamido]-3-cephem-4-carboxylic acid A. Preparation of 2-(tert-buthoxycarbonylprop-2-oxyimino)malononitrile 2-(hydroxyimino)malononitrile (95g) and tert-butyl-2-bromo-2-methyl propionate (240g) were reacted in the same method as described in (B) of Preparation 25 to give the above-indicated compound (176g).

b.p. : 115~120ºC/13 torr

NNR : δ (CDCl₃)

1.48(s, 9H), 1.63(s, 6H)

B. Preparation of 2-(tert-butoxycarbonylprop-2-oxyimino)-2-cyanoacetamidinium acetate

To ammonium acetate (18.5g) dissolved in methanol (100mℓ) was added 2-(tert-butoxycarbonylprop-2-oxyimino)malononitrile (19g).

After stirring for 2 hours, the mixture was allowed to stand overnight at room temperature. The reaction mixture was concentrated, and water (500mℓ) was added thereto. The obtained mixture was extracted with ethylacetate (500mℓ). After the extract was dehydrated, filtered, and concentrated, ethyl ether was added thereto, and the mixture stirred for 30 minutes.

The precipitates were filtered to give the above-indicated compound (15g) in pale yellow.

NMR : δ (DHSO-d₅)

1.40(s, 9H), 1.60(s, 6H), 1.98(s, 3H), 7.38(bs, 3H).

C. Preparation of 2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(tert- butoxycarbonylprop-2-oxyimino)acetonitrile

2-(tert-butoxycarbonylprop-2-oxyimino)-2-cyanoacetamdinium acetate (24.1g) was reacted in the same method as described in (D) of Preparation 25 to give the above-indicated compound (13.7g).

NMR : δ (DHSO-d₅)

1.40(s, 9H), 1.58(s, 6H), 8.43(s, 2H). D. Preparation of 2-(5-amino-1,2,4,-thiadiazol-3-yl)-2-(2- carboxyprop-2-oxyimino)acetic acid

2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(2-butoxycarbonylprop-2-oxyimino) acetonitrile (13.7g) was reacted in the same method as described in (E) of Preparation 25 to give the above-indicated compound (10.1g).

NMR : δ (DMSO-d₅).

1.42(s, 6H), 8.22(s, 2H).

E. Preparation of 3-acethoxymethyl-7-[(Z)-2-(5-amino-1,2,4- thiadiazol-3-yl)-2-(2-carboxyprop-2-oxyimino)acetamido]-3- cephem-4-carboxylic acid

2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(2-carboxyprop-2-oxyimino)acetic acid (2.93g) was reacted in the same method as described in (F) of Preparation 25 to give the above-indicated compound (3.42g).

NMR : δ (D₂O + NaHCO₃)

1.58(8, 6H), 2.05(s, 3H) , 3.10~3.72(ABq, 2H), 4.60~4.95

(ABq, 2H), 5.14(d, 1H), 5.70(d, 1H).

Example 1 : Synthesis of 7-[(Z)-2-(2-aminothiazol-4-yl)-2-(methoxyimino) acetamido]-3-(4,6-diamino-1-methylpyrimidinium-2-yl)thiomethyl -3-cephem-4-carboxylate

To a solution of 3-acetoxymethyl-7-[(Z)-2-(2-aminothiazol-4-yl)- 2-methoxyimino) acetamido]-3-cephem-4-carboxylic acid(500mg) suspended in distilled water(5m5) were added 4,6-diamino-1-methyl-2(1H)-pyrimidinethione(200mg) and potassium iodide(800mg). While adjusting the pH of the mixture to 7.1~7.2 with a sodium bicarbonate solution, the reaction mixture was heated to 70ºC. After stirred for 4 hours, the mixture was cooled to room temperature. The pH was adjusted to 3~3.5 with 2N hydrochloric acid, and the precipitates were filtered, washed with distilled water(5mℓ) , and chromatographed over silica gel. Elution with a 5 : 1 (v/v) mixture of acetonitrile/distilled water gave the above-indicated compound(320rag) in a pale white solid.

m.p. : 157ºC~(decomp.)

NMR : δ (D₂O + NaHCO₃)

3.54 (s, 3H). 3.61 (ABq, 2H), 3.98 (s, 3H).5.17 (d. 1H), 5.65 (s. 1H), 5.78 (d, 1H), 7.03 (s, 1H).

HS(FAB, H + 1) : 552

IR(KBr. cm^-1) : 1765 (β-lactam), 1660, 1630, 1550.

Example 2 : Synthesis of 7-[(Z)-2-(2-aminothiazol-4-yl)-2-(ethoxyimino) acetamido]-3-(4,6-diamino-1-methyl-pyrimidinium-2-yl)thiomethyl -3-cephem-4-carboxylate

3-Acetoxymethyl-7-[(Z)-2-(2-aminothiazol-4-yl)-2-(ethoxyimino) acetamido]-3-cephem-4-carboxylic acid (500mg) was reacted in the same manner as described in Example 1 to give the above-indicated compound (310mg) in a white solid.

m.p. : 163ºC~(decomp.)

NHR : δ (D₂O + NaHCO₃) 1.09 (t, 3H), 3.48 (s, 3H), 3.56 (ABq, 2H), 4.14 (q, 2H), 5.11 (d, 1H), 5.56 (s, 1H), 5.78 (d, 1H), 6.94 (s, 1H).

MS(FAP. H + 1) : 566

IR(KBr. cm^-1) : 1760 (β-lactam), 1660, 1590.

Example 3 : Synthesis of 7-[(Z)-2-(2-aminothiazol-4-yl)-2-(ethoxyimino) acetamido]-3-(4,6-diamino-1-ethylpyrimidinium-2-yl)thiomethyl -3-cephem-4-carboxylate To a solution of 3-acetoxymethyl-7-[(Z)-2-(2-aminothiazol-4-yl)-2-(ethoxyimino)acetamido]-3-cephem-4-carboxylic acid (500mg) suspended in distilled water (5mℓ) were added 4,6-diamino-1-ethyl-2(1H)-pyrimidinethione (200mg) and potassium iodide (1g). With adjusting pH of the mixture to pH 7.1~7.2 with a sodium bicarbonate solution, the reaction mixture was heated to 70ºC. After stirred for 5 hours, the mixture was cooled to room temperature. The pH was adjusted to 3~ 3.5 with 2N hydrochloric acid, and the precipitates were filtered, washed with distilled water (5mℓ), and chromatographed over silica gel.

Elution with a 5 : 1 (v/v) mixture of acetonitrile/distilled water gave the above-indicated compound(290mg) in a pale white solid.

m.p. : 161ºC~(decomp.)

NMR : δ (D₂O + NaHCO₃)

1.31 (m, 6H), 3.60 (ABq, 2H), 4.19 (m, 4H), 4.43 (ABq, 2H), 5.19 (d, 1H), 5.66 (s, 1H), 5.84 (d, 1H), 6.92 (s, 1H).

MS(FAB. M + 1) : 580

IR(KBr. cm^-1) : 1768 (β-lactam), 1680, 1620, 1560. Example 4 : Synthesis of 3-(1-allyl-4,6-diaminopyrimidinium-2-yl)- thiomethyl-7-[(Z)-2-(2-aminothiazol-4-yl)-2-(ethoxyimino) acetamido]-3-cephem-4-carboxylate To a solution of 3-acetoxymethyl-7-[(Z)-2-(2-aminothiazol-4-yl)-2-(ethoxyimino)acetamido]-3-cephem-4-carboxylic acid (500mg) suspended in distilled water (5mℓ) were added 1-allyl-4,6-diamino-2(1H)- pyrimidinethione (200mg) and potassium iodide (1g). The pH of the mixture was adjusted to 7.1~7.2 with a sodium carbonate solution, and acetonitrile (1mℓ) . was added thereto. After stirring for 4 hours at 75ºC, the mixture was cooled to room temperature. The pH was adjusted to 3~3.5 with 2N hydrochloric acid, and the precipitates were filtered, washed with distilled water (5mℓ), and chromatographed over silica gel. Elution with a 5 : 1 (v/v) mixture of acetonitrile/distilled water gave the above-indicated compound(300mg) in a white solid.

m.p. : 165ºC~(decomp.)

NMR : ό-(D₂O + NaHCO₃)

1.29 (t, 3H), 3.57 (ABq, 2H) , 4.17 (q, 2H) , 5.16 (d, 1H) , 5.66 (s, 1H), 5.82 (d, 1H), 5.09~6.56 (m, 5H), 6.96 (s, 1H).

MS(FAB. M+ l) : 592

IR(KBr. cm-¹) : 1765 (β-lactam), 1680, 1630, 1550.

Example 5 : Synthesis of 7-[(Z)-2-(2-aminothiazol-4-yl)-2-(2-propen-1- oxyimino)acetamido]-3-(4,6-diamino-1-methylpyrimidinium-2-yl) thiomethyl-3-cephem-4-carboxylate

A solution of 3-acetoxymethyl-7-[(Z(-2-(2-aminothiazol-4-yl)-2- (2-propen-1-oxyimino)acetamido]-3-cephem-4-carboxylic acid (500mg) suspended in distilled water (5mℓ) was reacted in the same manner as described in Example 1 to give the above-indicated compound (260mg) in a pale white solid.

w.P. : 169ºC~(decomp.)

NMR : 5(D_zO + acetone-d₅)

3.60 (ABq, 2H) , 3.61 (s, 3H) , 4.40 (ABq, 2H), 5.16 (d, 1H), 5.68 (s, 1H), 5.84 (d, 1H), 5.11~6.25 (m, 5H), 6.96 (s, 1H).

MS(FAB. M + 1) : 578

IR(KBr. cm^-1) : 1760 (β-lactam), 1670, 1618, 1522.

Example 6 : Synthesis of 7-[(Z)-2-(2-aminothiazol-4-yl)-2-(2-propen-1- oxyimino)acetamido]-3-(4,6-diamino-1-ethylpyrimidinium-2-yl) thiomethyl-3-cephem-4-carboxylate

3-Acetoxymethyl-7-[(Z)-2-(2-aminothiazol-4-yl)-2-(2-propen-1-oxyimino) acetamido]-3-cephem-4-carboxylic acid (500mg) and 4,6-diamino-1-ethyl-2(1H)-pyrimidinethione (200mg) were reacted in the same manner as described in Example 1 to give the above-indicated compound (290mg).

m.P. : 165ºC~(decomp.)

NMR : 5 (D₂O + acetone-d₅)

1.41 (t, 3H), 3.57 (ABq, 2H), 4.14 (q, 2H), 4.41 (ABq, 211), 5.16 (d, 1H), 5.67 (s, 1H), 5.84 (d, 1H), 5.05~6.12 (m, 5H), 6.96 (s, 1H). MS(FAB. M + 1) : 592

IR(KBr. cm^{- 1}) : 1764 (β-lactam), 1765, 1615, 1522. Example 7 : Synthesis of 3-(1-allyl-4,6-diaminopyrimidinium-2-yl)thiometlιyl -7-[(Z)-2-(2-aminothiazol-4-yl)-2-(propen-1-oxyimino)acetamido] -3-cephem-4-carboxylate 3-Acetoxymethyl-7-[(Z)-2-(2-aminothiazol-4-yl)-2-(2-propene-1-oxyimino) acetamido]-3-cephem-4-carboxylic acid (500mg) and 1-allyl-4,6-diamino-2(1H)-pyrimidinethione (200mg) were reacted in the same manner as described in Example 1 to give the above-indicated compound (310mg).

NMR : δ (D₂O + acetone-d₅)

3.56 (ABq, 2H), 4.39 (ABq, 2H) , 5.16 (d, 1H), 5.62 (s, 1H) , 5.79 (d, 1H), 5.08~6.21 (m, 10H), 7.01 (s, 1H).

MS(FAB, M + l) : 604

IR(KBr. cm-¹) : 1770 (β-lactam), 1669, 1620, 1531. Example 8 : Synthesis of 7-[(Z)-2-(2-aminothiazol-4-yl)-2-(2-propyn-1- oxyimino)acetamido]-3-(4,6-diamino-1-methylpyrimidinium-2-yl) thiomethyl-3-cephem-4-carboxylate

To a solution of 3-acetoxymethyl-7-[(Z)-2-(2-aminothiazol-4-yl)-2- (2-propyn-1-oxyimino)acetamido]-3-cephem-4-carboxylic acid (500mg) suspended in distilled water (5mℓ) were added 4,6-diamino-1-methyl-2(lH)- pyrimidinethione (200mg) and potassium iodide (lg). While adjusting the pH of the mixture to 7.1~7.2 with a sodium bicarbonate solution, the reaction mixture was heated to 70ºC. After stirring for 4 hours, the mixture was cooled to room temperature. The pH was adjusted to 3~3.5 with 2N hydrochloric acid, and the precipitates were filtered, washed with distilled water (5mℓ), and chromatographed over silica gel. Elution with a 5 : 1 (v/v) mixture of acetonitrile/distilled water gave the above-indicated compound (300mg) in a pale white solid.

m.p. : 167ºC~(decomp.)

NMR : δ (D₂O + acetone-d₅)

3.01 (s, 1H). 3.56 (s. 3H), 3.62 (ABq, 2H), 4.76 (s. 2H), 5.12 (d. 1H), 5.65 (s, 1H), 5.79 (d, 1H), 6.96 (s, 1H).

MS(FAB. M + 1) : 576

IR(KBr. cm^-1) : 1766 ( β-lactam), 1685, 1632, 1525. Example 9 : Synthesis of 7-[(Z)-2-(2-aminothiazol-4-yl)-2-(2-propyn-1- oxyimino)acetamido]-3-(4,6-diamino-1-ethylpyrimidinium-2-yl) thiomethyl-3-cephem-4-carboxylate

3-Acetoxymethyl-7-[(Z)-2-(2-aminothiazol-4-yl)-2-(2-propyn-1-oxyimino) acetamido]-3-cephem-4-carboxylic acid (500mg) and 4,6-diamino-1-ethyl-2(1H)-pyrimidinethione(200mgj were reacted in the same manner as described in Example 1 to give the above-indicated compound (280mg).

m.p. : 165ºC~(decomp.)

NMR : δ (D₂O + acetone-d₅)

1.41 (t, 3H), 3.03 (s, 1H), 3.56 (ABq, 2H) , 4.16 (q, 211), 4.39 (ABq,

2H), 4.81 (s, 2H), 5.16 (d, 1H), 5.66 (s, 1H), 5.84 (d, 1H), 7.00 (s, 1H).

MS(FAB, M + l) : 590

IR(KBr. cm^-1) : 1769 (β-lactam), 1781, 1630, 1525. Example 10 : Synthesis of 3-(1-allyl-4,6-diaminopyrimidinium-2-yl) thiomethyl- 7-[(Z)-2-(2-aminothiazol-4-yl)-2-(2-propyn-1- oxyimino)acetamido]-3-cephem-4-carboxylate 3-Acetoxymethyl-7-[(Z)-2-(2-aminothiazol-4-yl)-2-(2-propyn-1-oxyimino) acetamido]-3-cephem-4-carboxylic acid (500mg) and 1-allyl-4,6-diamino-2(1H)-pyrimidinethione (200mg) were reacted in the same manner as described in Example 1 to give the above-indicated compound (270mg). m.p. : 171ºC~(decomp.)

NMR : δ (D₂O + acetone-da)

3.02 (S, 1H), 3.57 (ABq, 2H), 4.43 (ABq, 2H), 4.79 (s, 2H), 5.18 (d, 1H), 5.63 (s, 1H), 5.79 (d, 1H), 5.12^6.31 (m, 5H), 6.97 (s, 1H). MS(FAB. M + 1) : 602

IR(KBr. cm^-1) : 1765 (β-lactam), 1660, 1620, 1530.

Example 11 : Synthesis of 7-[(Z)-2-(2-aminothiazol-4-yl)-2-(2-carboxyprop- 2-oxyimino)acetamido]-3-(4,6-diamino-1-methylpyrimidinium-2-yl) thiomethyl-3-cephem-4-carboxylate To a solution of 3-acetoxymethyl-7-[(Z)-2-(2-aminothiazol-4-yl)-2- (carboxyprop-2-oxyimino)acetamido]-3-cephem-4-carboxylic acid (500mg) suspended in distilled water (5mℓ) were added 4,6-diamino-1-methyl-2(1H)- pyrimidinethione (200mg) and potassium iodide (1.2g). While adjusting the pH of the mixture to 7.3~7.5 with a sodium bicarbonate solution, the reaction mixture was heated to 70ºC. After stirring for 4 hours, the mixture was cooled to room temperature. Insoluble materials were removed by filtration, and the pH of the filtrate was adjusted to 4 with 2N-hydrochloric acid. The precipitates were filtered, washed with distilled water (5mℓ), and chromatographed over silica gel. Elution with a 5 : 1 (v/v) mixture of acetonitrile/distilled water gave the above-indicated compound (280mg) in a pale white solid. m.p. : 151ºC~(decomp.)

NMR : δ (D₂O + NaHCO₃)

1.50 (s, 6H), 3.50 (s, 3H), 3.59 (ABq, 2H), 4.29 (ABq, 2H), 5.17 (d, 1H), 5.58 (s, 1H). 5.79 (d, 1H), 6.95 (s, 1H).

MS(FAH, M + l) : 624

IR(KBr. cm^-1) : 1761 (β-lactam), 1660, 1580, 1550.

Example 12 : Synthesis of 7-[(Z)-2-(2-aminothiazol-4-yl)-2-(2-carboxyprop

-2-oxyimino)acetamido]-3-(4,6-diamino-1-ethylpyrimidinium-2- yl)thiomethyl-3-cephem-4-carboxylate

3-Acetoxymethyl-7-[(Z)-2-(2-aminothiazol-4-yl)-2-(2-carboxyprop-2-oxyimino)acetamido]-3-cephem-4-carboxylic acid dihydrochloride (500mg) and 4,6-diamino-1-ethyl-2(1H)-pyrimidinethione (200mg) were reacted in the same manner as described in Example 11 to give the above-indicated compound (310mg) in a pale white solid.

m.p. : 153ºC~(decomp.)

NMR : .5 (D₂O + NaHCO₃)

1.32 (t, 3H), 1.48 (s, 6H), 3.56 (ABq, 2H), 4.04 (q, 2H), 4.31 (ABq, 2H), 5.12 (d, 1H), 5.53 (s, 1H) , 5.73 (d, 1H), 6.92 (s, 1H).

MS(FAB. M + 1) : 638

IR(KBr. cm^-1) : 1770 (β-lactam), 1680, 1590, 1530. Example 13 : Synthesis of 7-[(Z)-2-(2-aminothiazol-4-yl)-2-(2-carboxyprop -2-oxyiιino)acetamido]-3-(4,6-diamino-1-propylpyrimidinium-2- yl)thiomethyl-3-cephem-4-carboxylate To a solution of 3-acetoxymethyl-7-[(Z)-2-(2-aminothiazol-4-yl)-2-(2-carboxyprop-2-oxyimino)acetamido]-3-cephem-4-carboxylic acid dihydrochloride (500mg) dissolved in distilled water (10mℓ) were added 4,6-diamino-1-propyl-2(1H)-pyrimidinethione (200mg) and potassium iodide (1.2g). The pH of the mixture was adjusted to 7.3~7.4 with a sodium bicarbonate solution, and acetonirile (3mℓ) was added thereto. After stirring for 5 hours at 73ºC, the mixture was cooled to room temperature, and the acetonitrile was removed under reduced pressure. Insoluble materials were filtered off, and pH of the filtrate was adjusted to 4.5 with 2N-hydroehlorie acid. After being concentrated under reduced pressure, the residue was chromatographed over silica gel. Elution with a 5 : l(v/v) mixture of acetonitrile/distilled water gave the above-indicated compound (210mg) in a pale yellow solid. m.p. : 156ºC~(decomp.)

NMR : δ (D₂O + NaHCO_s)

0.93 (t, 3H), 1.49 (s, 6H), 1.77 (m, 2H), 3.61 (ABq, 2H), 3.91 (t,

2H), 5.14 (d, 1H), 5.54 (s, 1H) , 5.77 (d, 1H), 6.92 (s, 1H).

MS(FAB. M+ l) : 652

IR(KBr. cm^-1) : 1765 (β-lactam), 1650, 1596, 1530. Example 14 : Synthesis of 7-[(Z)-2-(2-aminothiazol-4-yl)-2-(2-carboxyprop -2-oxyimino)acetamido]-3-(1-butyl-4,6-diaminopyrimidinium-2- yl)thiomethyl-3-cephem-4-carboxylate 3-Acetoxymethyl-7-[(Z)-2-(2-aminothiazol-4-yl)-2-(2-carboxyprop-2-oxyimino)acetamido]-3-cephem-4-carboxylic acid dihydrochloride (500mg) and 1-butyl-4,6-diamino-1-2(1H)-pyrimidinethione (200mg) were reacted in the same manner as described in Example 13 to give the above indicated-compound (230mg).

_____ : 161ºC~(decomp.)

NMR : δ (D₂O + acetone-do)

0.92 (t, 3H), 1.36 (m, 2H), 1.48 (s, 611), 1.71 (m, 211), 3.52 (ABq, 2H), 3.99 (t, 2H), 4.35 (ABq, 2H) , 5.14 (d, 1H), 5.58 (s, III), 5.79 (d, 1H), 6.95 (s, 1H).

MS(FAH, M + 1) : 666

IR(KBr. cm^-1) : 1768 (β-lactam), 1671, 1625, 1528.

Example 15 : Synthesis of3-(1-allyl-4,6-diaminopyrimidinium-2-yl)thiomethyl

-7-[(Z)-2-(2-aminothiazol-4-yl)-2-(2-carboxyprop-2-oxyimino) acetamido]-3-cephem-4-carboxylate

3-Acetoxymethyl-7-[(Z)-2-(2-aminothiazol-4-yl)-2-(2-carboxyprop-2-oxyimino)acetamido]-3-cephem-4-carboxylic acid dihydrochloride (500mg) and 1-allyl-4,6-diamino-2(1H)-pyrimidinethione (200mg) were reacted in the same manner as described in Example 13 to give the above-indicated compound (310mg).

m.p. : 160ºC~(decomp.) NMR : δ (D₂O + acetone-d₅)

1.48 (s, 6H). 3.56 (ABq. 2H). 5.16 (d. 1H), 5.61 (s, 1H), 5.79 (d, 1H), 5.05~6.5l (m, 5H), 6.96 (s, 1H).

MS(FAB. H . 1) : 650

IR(KBr. cm^-1) : 1765 (β-lactam), 1670, 1620, 1530.

Example 16 : Synthesis of 7-[(Z)-2-(2-aminothiazol-4-yl)-2-(l-carboxyeth

-1-oxyimino)acetamido]-3-(4,6-diamino-1-methylpyrimidinium-2- yl)thiomethyl-3-cephem-4-carboxylate

To a solution of 3-acetoxymethyl-7-[(Z)-2-(2-aminothiazol-4-yl)-2-(2-carboxyeth-2-oxyimino)acetamido)-3-cephem-4-carboxylic acid (500mg) suspended in distilled water (10mℓ) were added 4,6-diamino-1-methyl-2(1H)-pyrimidinethione (200mg) and potassium iodide (1.2g). While adjusting the pH of the mixture to 7.1~7.2 with a sodium bicarbonate solution, the reaction mixture was heated to 70ºC. After stirring for 5 hours, the mixture was cooled to room temperature. The pH was adjusted to 4.1 with 2N-hydrochloric acid, and the precipitates were filtered, washed with distilled water (5mℓ), and chromatographed over silica gel. Elution with a 5 : 1 (v/v) mixture of acetonitrile/distilled water gave the above-indicated compound (200mg) in a pale white solid.

m.p. : 153ºC~(decomp.)

NHR : δ(D₂O + NaHCO₃)

1.48 (d, 3H), 3.53 (s, 3H), 3.59 (ABq, 2H), 4.36 (ABq, 2H), 5.17 (d, 1H), 5.60 (s, 1H), 5.79 (d, 1H), 7.01 (s, 1H).

MS(FAB, M + 1) ; 610

IR(KBr. cm^-1) : 1766 (β-lactam), 1765, 1595, 1525. Example 17 : Synthesis of 7-[ (Z)-2-(2-aminothiazol-4-yl)-2-(2-carboxyeth -1-oxyimino)acetamido]-3-(1-ethyl-4,6-diaminopyrimidinium-2- yl)thiomethyl-3-cephem-4-carboxylate 3-Acetoxymethyl-7-[ (Z)-2-(2-aminothiazol-4-yl)-2-(2-carboxyeth-1-oxyimino)acetamido]-3-cephem-4-carboxylic acid (500mg) and 4,6-diamino- 1-ethyl-2(1H)-pyrimidinethione (200mg) were reacted in the same manner as described in Example 16 to give the above-indicated compound(210mg). m.p. : 155ºC~(decomp.)

NMR : δ(D₂O+ acetone-d₅)

1.34 (t, 3H), 1.48 (d, 3H), 3.59 (ABq, 2H), 4.04 (q, 2H), 5.15 (d, 1H), 5.52 (s, 1H), 5.78 (d, 1H), 6.96 (s, 1H).

MS(FAB. M + 1) : 624

IR(KBr. cm^-1) : 1765 (β-lactam), 1765, 1590, 1530.

Example 18 : Synthesis of 7-[(Z)-2-(2-aminothiazol-4-yl)-2-(2-carboxyeth

-1-oxyimino)acetamido]-3-(4,6-diamino-1-propylpyrimidinium-2- yl)thiomethyl-3-cephem-4-carboxylate 3-Acetoxymethyl-7-[(Z)-2-(2-aminothiazol-4-yl)-2-(2-carboxyeth-1-oxyimino)acetamido]-3-cephem-4-carboxylic acid (500ag) and 4,6-diamino-1-propyl-2(1H)-pyrimidinethione (200mg) were reacted in the same manner as described in Example 16 to give the above-indicated compound (170mg).

m.p. : 154ºC~ (decomp.)

NMR ; δ (D₂O + NaHCO₃) 0.95 (t. 3H) , 1.46 (d, 3H) , 1.65 (m, 211) , 3.56 (ABq, 2H) , 3.91 (t, 211) , 5.17 (d, 1H) , 5.56 (s, 1H) , 5.77 (d, 1H) , 6.96 (s, 1H) .

MS(FAB. M + 1) : 638

IR(KBr. cm^-1) : 1760 (β-lactam) , 1671, 1590, 1525.

Example 19 : Synthesis of 3-(1-allyl-4,6-diaminopyrimidinium-2-yl)thiomethyl

-7-[ (Z)-2-(2-aminothiazol-4-yl)-2-(carboxyeth-2-oxyimino) acetamido]-3-cephem-4-carboxylate 3-Acetoxymethyl-7-[ (Z)-2-(2-aminothiazol-4-yl)-2-(2-carboxyeth-1-oxyimino)acetamido]-3-cephem-4-carboxylic acid (500mg) and 1-allyl-4,6-diamino-2(1H)-pyrimidinethione (200 mg) were reacted in the same manner as described in Example 16 to give the above-indicated compound(230mg). m.p, : 155ºC~(decomp.)

NMR : δ (D₂O + acetone-d₅)

1.44 (d, 3H), 3.52 (ABq, 2H) , 5.16 (d, 1H), 5.59 (s, 1H), 5.76 (d, 1H), 5.07~6.51 (m, 5H), 6.99 (s, 1H) .

MS(FAB. M + 1) : 636

IR(KBr. cm^-1) : 1765 (β-lactam), 1680, 1600, 1530.

Example 20 : Synthesis of 7-[(Z)-2-(2-aminothiazol-4-yl)-2-(1-carboxymethoxyimino)acetamido]-3-(4,6-diamino-1-methylpyrimidinium-2-yl) thiomethyl-3-cephem-4-carboxylate To a solution of 3-acetoxymethyl-7-[(Z)-2-(2-aminothiazol-4-yl)-2- (2-carboxymethoxyimino)acetamido]-3-cephem-4-carboxylic acid (500mg) suspended in distilled water (10mℓ) were added 4,6-diamino-1-methyl-2(1H)- pyrimidinethione (200mg) and potassium iodide (1.2g). With the adjusting of the pH of the mixture to 7.2 with a sodium bicarbonate solution, the reaction mixture was stirred for 5 hours at 70°C. After the mixture cooled to room temperature, insoluble materials were filtered off, and the pH of the filtrate was adjusted to 4.1 with 2N-hydrochloric acid. After being concentrated under reduced pressure, the residue was chromatographed over silica gel. Elution with a 4 : 1 (v/v) mixture of acetonitrile/distilled water gave above-indicated compound(350mg) in a white solid.

m.p. : 167ºC~(decpmp.)

NMR : δ (D₂O + NaHCO₃)

3.49 (s, 3H), 3.52 (ABq, 2H), 4.34 (ABq, 211), 4.60 (s, 211), 5.16 (d, 1H), 5.56 (s, 1H), 5.78 (d, 1H), 6.98 (s, 1H).

MS(FAB. H + 1) : 596

IR(KBr. cm^-1) : 1760 (β-lactam) , 1670, 1600, 1550.

Example 21 : Synthesis of 7-[(Z)-2-(2-aminothiazol-4-yl)-2-(carboxymethoxyimino)acetamido]-3-(4,6-diamino-1-ethylpyrimidinium-2- yl)thiomethyl-3-cephem-4-carboxylate

3-Acetoxymethyl-7-[(Z)-2-(2-aminothiazol-4-yl)-2-(2-carboxymethoχyimino)acetamido]-3-cephem-4-carboxylic acid (500 mg) and 4,6-diamino-1-ethyl-2(1H)-pyrimidinethione (200 mg) were reacted in the same manner as described in Example 20 to give the above-indicated compound(280mg).

m.p. : 165°C~(decomp.)

NMR : δ (D₂O + NaHC0₃)

1.32 (t, 3H), 3.62 (ABq, 2H), 3.98 (q, 2H) , 4.60 (s, 211), 5.17 (d, 1H), 5.58 (s.1H), 5.80 (d, 1H), 7.01 (s, 1H).

MS(FAP. M + 1) : 610

IR(KBr. cm^-1) : 1765 (β-lactam), 1670, 1600, 1520. Example 22 : Synthesis of 7-[(Z)-2-(2-aminothiazol-4-yl)-2-(carboxymethoxyimino)acetamido]-3-(4,6-diamino-1-propylpyrimidinium-2- yl)thiomethyl-3-cephem-4-carboxylate

3-Acetoxymethyl-7-[(Z)-2-(2-aminothiazol-4-yl)-2-(2-carboxymethoxyimino) acetamido]-3-cephem-4-carboxylic acid (500mg) and4,6-diamino-1-propyl- 2(1H)-pyrimidinethione (200mg) were reacted in the same manner as described in Example 20 to give the above-indicated compound(2lOmg).

m.p. : 169ºC~(decomp.)

NMR : δ (D₂O + NaHCO₃)

0.93 (t, 3H), 1.73 (m, 2H) , 3.56 (ABq, 2H) , 3.92 (t, 2H) , 4.58 (s,

2H), 5.15 (d, 1H), 5.56 (s, 1H), 5.78 (d, 1H), 6.98 (s, 1H) .

HS(FAB, M + l) : 624

IR(KBr. cm^-1) : 1763 (β-lactam), 1670, 1610, 1525. Example 23. Synthesis of 7-[(Z)-2-(2-aminothiazol-4-yl)-2-(carboxymethoxyimino)acetamido]-3-(1-butyl-4,6-diaminopyrimidinium-2- yl)thiomethyl-3-cephem-4-carboxylate

3-Acetoxymethyl-7-[(Z)-2-(2-aminothiazol-4-yl)-1-(2-carboxymethoxyimino) acetamido]-3-cephem-4-carboxylic acid (500mg) and 1-butyl-4,6-diamino- 2(1H)-pyrimidinethione (200mg) were reacted in the same manner as described in Example 20 to give the above-indicated compound(240mg). m.p. : 1674,C~(decomp.)

NMR : δ (D₂O + NaHCO₃)

0.92 (t, 3H), 1.32 (m, 2H) , 1.66 (m, 2H), 3.60 (ABq, 2H), 3.96 (t, 2H), 4.57 (s, 2H), 5.15 (d, 1H) , 5.58 (s, 1H), 5.78 (d, 1H), 7.01 (s, 1H). MS(FAB. M + 1) : 638

IR(KBr. cm^-1) : 1765 ( β-lactam), 1670, 1610, 1530.

Example 24 : Synthesis of 3-(1-allyl-4,6-diaminopyrimidinium-2-yl)thiomethyl

-7-[(Z)-2-(2-aminothiazol-4-yl)-2-(2-carboxymethoxyimino)acetamido]-3-cephem-4-carboxylate

3-Acetoxymethyl-7-[(Z)-2-(2-aminothiazol-4-yl)-2-(2-carboxymethoxyimino) acetamido]-3-cephem-4-carboxylic acid (500mg) and 1-allyl-4,6-diamino-2(1H)-pyrimidinethione (200mg) were reacted in the same manner as described in Example 20 to give the above-indicated compound(220rag).

m.p. : 165ºC~(decomp.)

NMR : δ (D₂O + NaHCO₃)

3.56 (ABq, 2H), 4.56 (s, 2H), 5.12 (d, 1H), 5.63 (s, 1H), 5.79 (d, 1H), 6.07~6.51 (m, 5H), 7.00 (s, 1H).

MS(FAB. M + 1) : 622

IR(KBr. cm^-1) : 1770 (β-lactam), 1660, 1600, 1535.

Example 25 : Synthesis of 7-[(Z)-2-(2-aminothiazol-4-yl)-2-(methoxyimino) acetamido]-3-(1,4,6-triaminopyrimidinium-2-yl)thiomethyl-3- cephem-4-carboxylate

To a solution of 3-acetoxymethyl-7-[(Z)-2-(2-aminothiazol-4-yl)-2- (methoxyimino)acetamido]-3-cephem-4-carboxylic acid (500mg) suspended in distilled water (5mℓ) were added 1,4,6-triamino-2(1H)-pyrimidinethione (200mg) and potassium iodide (800mg) . With adjusting of the pll of the mixture to 7.1~7.2 with a sodium bicarbonate solution, the reaction mixture was heated to 70ºC. After stirring for 4 hours, the mixture was cooled to room temperature. The pH was adjusted to 3~3.5 with 2N-hydrochloric acid, and the precipitates were filtered, washed with distilled water (5mℓ), and chromatographed over silica gel. Elution with a 5 : l(v/v) mixture of acetonitrile/distilled water gave the above-indicated compound (300mg) in a pale white solid.

m.P. : 156ºC~(decomp.)

NMR ; δ (D₂O + acetone-d₅)

3.58 (ABq, 2H), 3.81 (s, 3H), 4.33 (ABq, 2H), 5.12 (d, 1H), 5.61 (s, 1H), 5.83 (d, 1H), 6.91 (s, 1H).

MS(FAB. M + 1) : 553

IR(KBr. cm^-1) : 1765 (β-lactam), 1670, 1620, 1560.

Example 26 : Synthesis of 7-[(Z)-2-(2-aminothiazol-4-yl)-2-(ethoxyimino) acetamido]-3-(1,4,6-triaminopyrimidinium-2-yl)thiomethyl-3- cephem-4-carboxylate

3-Acetoxymethyl-7-[(Z)-2-(2-aminothiazol-4-yl)-2-(ethoxyimino) acetamido]-3-cephem-4-carboxylic acid (500mg) was reacted in the same manner as described in Example 25 to give the above-indicated compound (290mg) in a pale white solid.

m.P. : 165ºC~(decomp.)

NMR : δ(D₂O + acetone-d₅) 1.29 (t , 2H) , 3.57 (ABq, 2H) , 4.24 (q , 2H) , 4.35 (ABq , 2H) , 5.16 (d , 1H) , 5.62 (s, 1H) , 6.91 (s , 1H) .

MS (FAB , M + 1 ) : 567

IR(KBr. cm-¹) : 1765 (β-lactam), 1680, 1590.

Example 27 : Synthesis of 7-[(Z)-2-(2-aminothiazol-4-yl)-2-(2-propyn

-1-oxyimino)acetamido]-3-(1,4,6-triaminopyrimidinium-2-yl) thiomethyl-3-cephem-4-carboxylate 3-Acetoxymethyl-7-[(Z)-2-(2-aminothiazol-4-yl)-2-(2-propyn-1-oxyimino) acetamido]-3-cephem-4-carboxylic acid (500mg) was reacted in the same manner as described in Example 25 to give the above-indicated compound (350mg) in a pale yellow solid.

m.P. : 167ºC~(decomp.)

NMR : δ (D₂O + acetone-d₀)

3.06 (t, 1H), 3.56 (ABq, 2H) , 4.41 (ABq, 2H) , 4.80 (d, 2H), 5.12 (d, 1H), 5.62 (s, 1H), 5.80 (d, 1H), 6.96 (s, 1H).

MS(FAB. M + 1) : 577

IR(KBr. cm^-1) : 1765 (£-lactam), 1690, 1580.

Example 28 : Synthesis of 7-[(Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2- (ethoxyimino)acetamido)-3-(1,4,6-triaminopyrimidinium-2-yl) thiomethyl-3-cephem-4-carboxylate 3-Acetoxymethyl-7-[(Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(ethoxyimino) acetamido]-3-cephem-4-carboxylic acid (500mg) was reacted in the same manner as described in Example 25 to give the above-indicated compound (280mg) in a yellow solid.

m.P. : 169ºC~(decomp.)

NMR : δ (D₂O. + acetone-d₅)

1.52 (t, 3H), 3.57 (ABq, 2H), 4.26 (ABq, 2H), 4.36 (q, 2H) , 5.14 (d, 1H), 5.58 (s, 1H), 5.84 (d, 1H).

IR(KBr, cm^-1) : 1769 (£-lactam), 1690, 1630.

Example 29 : Synthesis of 7-[(Z)-2-(2-aminothiazol-4-yl)-2-(carboxyprop- 2-oxyimino)acetamido]-3-(l,4,6-triaminopyrimidinium-2-yl) thiomethyl-3-cephem-4-carboxylate

To a solution of 3-acetoxymethyl-7-[(Z)-(2-aminothiazol-4-yl)-2-{2-carboxyprop-2-oxyimino)acetamido]-3-cephem-4-carboxylic acid (500mg) in distilled water (10mℓ) were added 1,4,6-triamino-2-(1H)-pyrimidinethione (200mg) and potassium iodide (1.2g). The pH of the reaction mixture was adjusted to 7.1~7.3 with a sodium bicarbonate solution, and the reaction mixture was heated for 4 hours to 70ºC. After cooling to room temperature, insoluble materials were filtered off, and the pH of the filtrate was adjusted to 4. After being concentrated under reduced pressure, the residue was chromatographed over silica gel. Elution with a 4:1 (v/v) mixture of acetonitrile/distilled water gave the above-indicated compound (310mg) in a pale white solid.

m.p. : 155ºC~ (decomp.)

NMR : δ (D₂O + NaHCO₃)

1.49 (s, 6H), 3.58 (ABq, 2H), 4.22 (ABq, 2H), 5.16 (d, 1H), 5.56 (s, 1H), 5.77 (d, 1H), 6.94 (s, 1H).

MS(FAB. M + 1) : 625 IR(KBr. cm^-1) : 1770 (β-lactam), 1690, 1610, 1570.

Example 30 : Synthesis of 7-[(Z)-2-(2-aminothiazol-4-yl)-2-(1-carboxyeth- 1-oxyimino)acetamido]-3-(1,4,6-triaminopyrimidinium-2-y1) thiomethyl-3-cephem-4-carboxylate

3-Acetoxymethyl-7-[(Z)-2-(2-aminothiazol-4-yl)-2-(l-carboxyeth-1-oxyimino)acetamido]-3-cephem-4-carboxylic acid (500mg) was reacted in the same Banner as described in Example 29 to give the above-indicated compound (230mg) in a pale yellow solid.

m.p. : 167ºC~(decomp.)

NMR : δ (D₂O + acetone-d₅)

1.44 (d, 3H), 3.55 (ABq, 211), 4.21 (ABq, 2H), 5.17 (d, 1H), 5.54 (s, 1H), 5.76 (d, 1H), 6.97 (s, 1H).

MS(FAB. M + 1) : 611

IR(KBr. cm^-1) : 1765 ( yG-lactam) , 1660, 1590 , 1540.

Example 31 : Synthesis of 7-[(Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(2- carboxyprop-2-oxyimino)acetamido]-3-(1,4,6-triaminopyrimidinium -2-yl)thiomethyl-3-cephem-4-carboxylate

3-Acetoxymethyl-7-[(Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(2-carboxyprop-2-oxyimino)acetamido]-3-cephem-4-carboxylic acid (500mg) was reacted in the same manner as described in Example 29 to give the above-indicated compound (280mg) in a pale white solid.

m.P. : 173*C~(decomp.)

NHR : δ (D₂O + NaHCO₃) 3.62 (s, 3H), 3.66 (ABq, 211), 4.05 (s, 3H), 4.45 (ABq, 211), 5.15 (s, 1H), 5.81 (d, 1H).

IR(KBr. cm^-1) : 1760 (β-lactam), 1690, 1610, 1570.

Example 32 : Synthesis of 7-[(Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2- (ιethoxyimino)acetamido]-3-(4,6-diamino-1-methylpyrimidiniua -2-yl)thiomethyl-3-cephem-4-carboxylate To a solution of 3-acetoxymetbyl-7-[(Z)-(5-amino-1,2,4-thiadiazol -3-yl)-2-(methoxyimino)acetamido]-3-cephem-4-carboxylic acid (500mg) suspended in distilled water (5mℓ) were added 4,6-diamino-1-methyl-2(1H)-pyrimidinethione (200mg) and potassium iodide (800mg). With adjusting of the pH of the mixture to 7.1~7.2 with a sodium bicarbonate solution, the reaction mixture was heated to 70°C.

After stirring for 4 hours, the mixture was cooled to room temperature. The pH was adjusted to 3~3.5 with 2N-hydrochloric acid, and the resultant precipitates were filtered, washed with distilled water (5mℓ), and chromatographed over silica gel. Elution with a 5 : 1(v/v) mixture of acetonitrile/distilled water gave the above-indicated compound(300mg) in a pale white solid.

m.P. : 161ºC~ (decomp.)

NMR : δ (D₂O + acetone-do)

3.62 (s, 3H), 3.66 (ABq, 2H) , 4.05 (s, 3H), 4.45 (ABq, 211), 5.15 (d, 1H), 5.62 (s, 1H), 5.81 (d, 1H).

IR(KBr. cm-¹) : 1765 (β-laetam), 1680, 1630, 1570. Example 33 : Synthesis of 7-[(Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2- (methoxyimino)acetamido]-3-(4,6-diamino-1-ethylpyrimidinium -2-yl)thiomethyl-3-cephem-4-carboxylate 3-Acetoxymethyl-7-[(Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(methoxyimino) acetamido]-3-cephem-4-carboxylic acid (500mg) and 4,6-diaraino-1-ethyl- 2(1H)-pyrimidinethione (200mg) were reacted in the same manner as described in Example 32 to give the above-indicated compound (230rag).

m.P. : 169ºC~ (decomp.)

NMR : δ (D₂O + acetone-d₅)

3.60 (q, 2H), 3.60 (ABq, 2H) , 4.05 (s, 3H) , 4.55 (ABq, 2H) , 5.11

(d, 1H), 5.68 (s, 1H), 5.82 (d, 1H).

IR(KBr. cm^-1) : 1770 (0-lactara), 1690, 1630, 1580. Example 34 : Synthesis of 7-[(Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2- (methoxyimino)acetamido]-3-(4,6-diamino-1-propylpyrimidinium -2-yl)thiomethyl-3-cephem-4-carboxylate

3-Acetoxymethyl-7-[(Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(methoxyimino)acetamido]-3-cephem-4-carboxylic acid (500mg) and 4,6-diamino-1-propyl-2(1H)-pyrimidinethione (200mg) were reacted in the same manner as described in Example 32 to give the above-indicated compound (250rag) .

m.P. : 67ºC~ (decomp.)

NMR : δ (D₂O + acetone-d₅,

1.05 (t, 3H), 1.80 (n, 2H), 3.52 (ABq, 2H) , 3.80 (t, 2H) , 4.05

(s. 3H), 4.55 (ABq, 2H), 5.16 (d, 1H), 5.65 (s, 1H), 5.84 (d, 1H).

IR(KBr. cm^-1) : 1765 (β-lactam), 1695, 1640, 1580. Example 35 : Synthesis of 7-[(Z)-2-(5-amino-1,2,4-thiadiazol-3-yl}-2- (methoxyimino)acetamido]-3-(1-allyl-4,6-diaminopyrimidiniuB -2-yl)thiomethyl-3-cephera-4-carboxylate 3-Acetoxymethyl-7-[(Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2- (methoxyimino)acetamido]-3-cephem-4-carboxylic acid (500mg) and 1-allyl-4, 6-diamino-2(1H)-pyrimidinethione (200mg) were reacted in the same manner as described in Example 32 to give the above-indicated compound(170mg).

m.P. : l58ºC~(decomp.)

NMR : δ (D₂O + acetone-d₅)

3.56 (ABq, 2H), 4.05 (s, 3H) , 4.42 (ABq, 2H), 5.16 (d, 1H), 5.70 (s, 1H), 5.85 (d, 1H), 5.05~6.51 (n, 511).

IR(KBr. cm^**1) : 1760 (£-lactam), 1700, 1650, 1590. Example 36 : Synthesis of 7-[(Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2- (ethoxyimino)acetaraido]-3-(4,6-diamino-1-methylpyriraidinium -2-yl)thiomethyl-3-cephem-4-carboxylate

3-Acetoxymethyl-7-[(Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(ethoxyimino) acetamido]-3-cephem-4-carboxylic acid (500mg) and 4,6-diamino-1-methyl- 2(1H)-pyrimidinethione (200mg) were reacted in the same manner as described in Example 32 to give the above-indicated compound (280rag).

m.p. : 163ºC~(decomp.)

NHR : β{D₂O + acetone-dβ)

1.30 (t, 311), 3.60 (s, 3H) , 3.56 (ABq, 211), 4.30 (q, 2H) , 4.40

(ABq, 2H), 5.13 (d, 1H) , 5.62 (s, 1H), 5.84 (d, 1H).

IR(KBr. cm^-1) : 1768 (β-lactam), 1690, 1630, 1580. Example 37 : Synthesis of 7-[(Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2- (ethoxyiraino)acetamido]-3-(4,6-diamino-1-ethylpyrimidinium -2-yl)thiomethyl-3-cephem-4-carboxylate 3-Acetoxymethyl-7-[(Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(ethoxyimino) acetamido]-3-cephem-4-carboxylic acid (500mg) and 4,6-diamino-1-ethyl-2(1H)-pyrimidinethione (200mg) were reacted in the same manner as described in Example 32 to give the above-indicated compound(270rog).

m.p. : 165ºC~ (decomp.)

NMR: δ (D₂O + acetone-dβ)

1.18 (t, 3H), 1.30 (t, 3H), 3.60 (q, 2IJ) , 3.58 (ABq, 211), 1.30 (q, 2H), 4.40 (ABq, 2H) , 5.18 (d, 1H) , 5.71 (s, 1H), 5.84 (d, 1H).

IR(KBr. cm^-1) : 1765 (β-lactam), 1695, 1630, 1570. Example 38 : Synthesis of 7-[(Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2- (ethoxyimino)acetamido]-3-(4,6-diamino-1-propylpyriraidinium -2-yl)thiomethyl-3-cephem-4-carboxylate

3-Acetoxymethyl-7-[(Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(ethoxyimino) acetamido]-3-cepheιs-4-carboxylic acid (500mg) and 4,6-diaraino-1-propyl-2(1H)-pyrimidinethione (200mg) were reacted in the same manner as described in Example 32 to give the above-indicated compound(230rag).

m.p. : 158ºC~ (decomp.)

NMR : δ (D_zO + acetone-dβ)

1.05 (t, 3H), 1.30 (t, 311), 1.80 (n, 2H), 3.54 (ABq, 2H), 4.0 (t,

2H), 4.32 (q, 2H) , 4.58 (ABq, 2H), 5.18 (d, 1H) , 5.69 (s, 1H).

5.84 (d, 1H). IR(KBr. cm^-1) : 1770 (β-lactam), 1690, 1640, 1680.

Example 39 : Synthesis of 7-[(Z)-2-(5-araino-1,2,4-thiadiazol-3-yl)-2- (ethoxyimino)acetamido]-3-(1-allyl-4,6-diaminopyrimidinium -2-yl)thiomethyl-3-cephem-4-carboxylate

3-Acetoxymethyl-7-[(Z)-2-(5-amino-1,2,4-thiadiazo1-3-yl)-2-(ethoxyimino) acetamido]-3-cephem-4-carboxylic acid (500mg) and 1-allyl-4,6-diamino-2(1H)-pyriιidinethione (200mg) were reacted in the same manner as described in Example 32 to give the above-indicated compound(210mg).

m.p. : 159ºC~ (decomp. )

NMR : δ (D₂0 + acetone-d₅)

1.31 (t, 3H), 3.60 (ABq, 2H) , 4.32 (q, 2H) , 4.42 (ABq, 211), 5.16 (d, 1H), 5.68 (s, 1H), 5.82 (d, 1H), 5.05~6.5l (m, 5H).

IR(KBr. cm^-1) : 1769(β-lactara), 1695, 1630, 1570.

Example 40 : Synthesis of 7-[(Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2- (2-carboxyprop-2-oxyimino)acetamido]-3-(4,6-diamino-1- methylpyrimidinium-2-yl)thiomethyl-3-cephem-4-carboxylate

To a solution of 3-acetoxymethyl-7-f (Z)-2-(5-amino-1,2,4-thiadiazol -3-yl)-2-(2-carboxyprop-2-oxyimino)acetamido]-3-cephem-4-carboxylic acid (500mg) suspended in distilled water (10mℓ) were added 4,6-diamino-1- methyl-2(1H)-pyrimidinethione (200mg) and potassium iodide (1.2g).

After adjusting the pH of the reaction mixture to 7.3~7.5 with a sodium bicarbonate solution, the reaction mixture was stirred for 4 hours at 70ºC. The mixture was cooled to room temperature, and insoluble materials were filtered off, and pll of the filtrate was adjusted to 4. After concentration under reduced pressure, the residue was chromatographed over silica gel. Elution with a 4 : 1 (v/v) mixture of acetonitrile/distilled water gave the above-indicated compound (200mg) in a pale white solid.

m.P. : 154ºC~(decomp.)

NMR : δ (D₂O + acetone-do)

1.52 (s, 6H), 3.51 (s, 3H), 3.58 (ABq, 2H), 4.40 (ABq, 211), 5.18 (d, 1H), 5.60 (s, 1H), 5.81 (d, 1H).

IR(KBr. cm^-1) : 1769 (β-lactam), 1700, 1650, 1590.

Example 41 : Synthesis of 7-[(Z)-2-(5-amino-1,2,4-thiadiazo]-3-yl)-2- (carboxyprop-2-oxyimino)acetamido]-3-(4,6-diamino-1- ethylpyrimidinium-2-yl)thiomethyl-3-cephem-4-carboxylate

3-Acetoxymethyl-7-[(Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(2-carboxyprop-2-oxyimino)acetamido]-3-cephem-4-carboxylic acid (500rag) and

4,6-diamino-1-ethy1-2(1H)-pyrimidinethione (200 mg) were reacted in the same manner as described in Example 40 to give the above-indicated compound(250mg).

m.P. : 161ºC~ (decomp.)

NMR : δ (D₂O + acetone-do)

1.32 (t, 3H), 1.58 (s, 6H) , 3.56 (ABq, 2H) , 4.02 (q, 2H), 4.43 (ABq, 2H), 5.18 (d, 1H), 5.58 (s, 1H) , 5.81 (d, 1H).

IR(KBr. cm^-1) : 1767 (β-lactam), 1695, 1640, 1580. Example 42 : Synthesis of 7-[(Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2- (2-carboxyprop-2-oxyimino)acetamido]-3-(4,6-diamino-1- propylpyrimidinium-2-yl)thiomethyl-3-cephem-4-carboxylate 3-Acetoxymethyl-7-[(Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(2-carboxyprop-2-oxyimino)acetamido]-3-cephera-4-carboxylic acid(500mg) and 4,6-diamino-1-propyl-2(1H)-pyrimidinethione (200mg) were reacted in the same manner as described in Example 40 to give the above-indicated compound(190mg).

m.P. : 159ºC~(decomp.)

NMR : δ (D₂O + acetone-d₅)

1.02 (t. 3H). 1.52 (s, 6H), 1.53 (m, 2H), 3.60 (ABq, 2H), 3.98 (t, 2H), 4.45 (ABq, 2H), 5.18 (d, 1H) , 5.58 (s, 1H). 5.81 (d, 1H) . IR(KBr. cm-¹) : 1765 ( β-lactam), 1690, 1630, 1570.

Example 43 : Synthesis of 7-{(Z)-2-(5-araino-1,2,4-thiadiazol-3-yl)-2- (2-carboxyprop-2-oxyimino)acetamido]-3-(l-butyl-4,6-diamino pyrimidinium-2-yl)thiomethyl-3-cephem-4-carboxylate 3-acetoxymethyl-7-[(Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(2- carboxyprop-2-oxyimino)acetamido]-3-cephem-4-carboxylic acid(500mg) and l-butyl-4,6-diamino-2(lH)-pyrimidinethione (200mg) were reacted in the same manner as described in Example 40 to give the above-indicated compound(160mg).

m.P. : 163ºC~ (decorap.)

NMR : δ (D₂O + acetone-dβ)

0.98 (t, 3H), 1.50 (m, 4H), 1.54 (s, 6H), 3.60 (ABq, 2H), 3.95 (t, 2H) , 4.46 (ABq, 2H) , 5.18 (d, III) , 5.58(s, 111) , 5.81 (d, 1H) .

IR(KBr. cm^-1) : 1770 ( /ff -lactam) , 1690, 1620, 1560.

Example 44 : Synthesis of 7-[ (Z)-2-(5-amino-l ,2, 4-thiadiazol-3-yl )-2- (2-carboxyprop-2-oxyimino)acetamido]-3-(1-allyl-4 ,6-diamino- pyrimidinium-2-yl)thiomethyl-3-cephem-4-carboxylate

3-Acetoxymethyl-7-[ (Z)-2-(5-amino-l ,2,4-thiadiazol-3-yl)-2-(2-carboxyprop-2-oxyimino)acetamido]-3-cephem-4-carboxylic acid (5OOrag) and 1-ally1-4,6-diamino-2(lH)-pyrimidinethione (200rag) were reacted in the same manner as described in Example 40 to give the above-indicated compound (210mg).

m.P. : 156ºC~(decomp.)

NMR: δ (D₂O + acetone-dβ)

1.58 (s, 6H), 3.60 (ABq, 2H) , 3.71 (d, 2H), 4.45 (ABq, 211), 5.18 (d, 1H), 5.60 (s, 1H), 5.81 (d, 1H), 5.01~6.5l (m, 3H).

IR(KBr. cm^-1) : 1760 (β-lactam), 1680, 1620, 1570.

Example 45 : Synthesis of 7-[(Z)-2-(2-aminothiazol-4-yl)-2-(2-carboxyprop

-2-oxyimino)acetamido]-3-(4,6-diamino-1,5-dimethylpyrimidinium -2-yl)thiomethyl-3-cephem-4-carboxylate

To 3-acetoxymethyl-7-[(Z)-2-(2-aminothiazol-4-yl)-2-(2-carboxyprop-1-oxyimino)acetaraido]-3-cephem-4-carboxylic acid (500mg) were added 4,6-diamino-1,5-dimethyl-2(1H)-pyrimidinethione (200mg) obtained in Preparation 7, potassium iodide (800mg) and distilled water (30mℓ) . With adjusting of the pH of the mixture to 7.0~7.5 with a saturated aqueous sodium bicarbonate solution, the reaction mixture was stirred for 4 hours at 70~75ºC. After the mixture was cooled to room temperature, the pH of the mixture was adjusted to 4.5~5.0 with 2N-hydrochloric acid.

The precipitates were collected by filteration and chromatographed over silica gel. Elution with a 7 : 1 (v/v) mixture of acetonitrile/ distilled water gave the above-indicated compound (126ag) in a pale yellow solid.

m.P. : 174'C~(decoraρ.)

NMR : δ (D₂P + NaHCO₃)

1.48 (s, 6H), 2.21 (s, 3H), 3.33 and 3.73 (ABq, 2H), 3.49 (s, 3H),

3.89 and 4.72 (ABq, 2H), 6.18 (d, 1H), 5.78 (d, 1H), 6.92 (s, 1H).

MS(FAB. M + 1) : 638

IR(KBr. cm^-1) : 1770 (/S-lactam), 1761, 1690, 1527. Example 46 : Synthesis of 7-[(Z)-2-(2-aminothiazol-4-yl)-2-(2-carboxyprop

-2-oxyimino)acetamido]-3-(4,6-diaιino-5-ethyl-1-Bethylpyrimidinium-2-yl)thiomethyl-3-cephem-4-carboxylate

The above-indicated compound (130mg) in a pale white solid was prepared in the same method as described in Example 45 except for using 4,6-diamino-1-ethyl-5-methyl-2(lH)-pyrimidinethione (200rag) obtained in Preparation 10 in place of 4,6-diamino-l,5-dimethyl-2(1H)-pyrimidinethione m.p. : 178°C~(decomp.)

NHR : δ(DMSO-d₅)

0.93 (t, 3H), 1.42 (d, 6H), 2.38 (q, 2H) , 3.19 and 3.54 (ABq, 2H),

3.49 (s, 3H), 3.85 and 4.80 (ABq, 2H), 4.96 (d, 1H), 5.68 (dd, 1H), 6.75 (s, 1H), 7.20 (s, 2H), 7.71 (bs, 4H), 11.42 (bs, 1H). HS (FAB. H t 1 ) : 662

IR(KBr. cm^-1) : 1769 (β-lactam), 1685, 1632, 1580.

Example 47 : Synthesis of7-((Z)-2-(2-aminothiazol-4-yl)-2-(2-carboxyprop

-2-oxyimino)acetamido]-3-(4,6-diamino-1-ethyl-5-methylpyrimidinium-2-yl)thiomethyl-3-cephera-4-carboxylate

The above-indicated compound (150mg) in a yellow solid was prepared in the same method as described in Example 45 except for using 4,6-diamino-1-ethyl-5-methyl-2(lH)-pyrimidinethione (200rag) obtained in Preparation 8 in place of 4,6-diamino-l,5-dimethyl-2(1H)-pyriraidinethione.

m.P. : 180ºC~(decomp.)

NHR : d(DHSO-d₅)

1.22 (t. 3H), 1.42 (d, 6H), 1.90 (s. 3H), 3.20 and 3.65 (ABq, 211), 3.89 and 4.78 (ABq, 2H), 4.10 (q, 2π), 4.98 (d, 1H), 5.70 (dd, 1H).

6.79 (s, 1H), 7.22 (s, 2H), 7.78 (bs, 4H), 11.24 (bs, 1H).

HS(FAB, H + 1) : 652

IR(KBr. cm^-1) : 1765 (β-lactan), 1685, 1630, 1680. Example 48 : Synthesis of 7-[(Z)-2-(2-aminothiazol-4-yl)-2-(2-carboxyprop

-2-oxyimino)acetamido]-3-(4,6-diamino-1,5-diethylpyrimidinium -2-yl)thiomethyl-3-cephem-4-carboxylate

The above-indicated compound (140mg) in a Pale yellow solid was prepared in the same method as described in Example 45 except for using 4,6-diamino-1,5-diethyl-2(1H)-pyrimidinethione (200 mg) obtained in Preparation 11 in place of 4,6-diamino-1,5-dimethyl-2(1H)-pyrimidinethione. m.P. : 168ºC~ (decomp. )

NMR : δ DMSO-d_a)

0.97 (t, 3H), 1.22 (t, 3H), 1.43 (d, 611), 2.40 (q, 2H), 3.20 and 3.56 (ABq, 2H), 3.84 and 4.81 (ABq, 2H), 4.08 (q, 2H), 4.98 (d, 1H). 5.70 (dd, 1H), 6.74 (s, 1H), 7.20 (s, 2H), 7.71 (bs, 4H), 11.45 (bs, 1H). MS(FAB. M+1) : 666

IR(KBr. cm^-1) : 1766 ( β-lactam), 1640, 1600.

Example 49 : Synthesis of 7-[(Z)-2-(2-aminothiazol-4-yl)-2-(2-carboxyprop

-2-oxyiraino)acetamido]-3-(5-methyl-l,4,6-triaminopyrimidinium-

-2-yl)thiomethyl-3-cephem-4-carboxylate

The above-indicated compound (170mg) in a Pale yellow solid was prepared in the same method as described in Example 45 except for using 5-methyl-1,4,6-triamino-2(1H)-pyrimidinethione (200mg) obtained in Preparation 9 in place of 4,6-diamino-l,5-dimethyl-2(1H)-pyrimidinethione. m.P. : 178ºC~(decomp.)

NMR : 5(DHSO-d_a)

1.43 (d, 6H), 1.82 (s, 3H), 3.19 and 3.48 (ABq, 2H), 3.72 and 4.52 (ABq, 2H), 4.99 (d, 1H), 5.68 (dd, 1H), 6.11 (s, 2H) , 6.73 (s, I1),

7.22 (s, 2H), 7.70 (bs, 4H), 11.31 (bs, 1H).

HS(FAB. M + 1) : 639

IR(KBr. cm^-1) : 1765 (β-lactara), 1628, 1590. Example 50 : Synthesis of 7-[(Z)-2-(2-aminothiazol-4-yl)-2-(2-carboxyprop -2-oxyimino)acetaraido]-3-(1-cyclopropyl-4,6-diaminopyrimidinium -2-yl)thiomethyl-3-cephem-4-carboxylate To a solution of 3-acetoxymethyl-7-[(Z)-2-(2-aminothiazol-4-yl)-2-(carboxyprop-2-oxyimino)acetamido]-3-cephem-4-carboxylic acid dihydrochloride (500mg) suspended in distilled water (10mℓ) were added 1-cyclopropyl-4,6-diamino-2(1H)-pyrimidinethione (200mg) and potassium iodide (1.2g). With adjusting of the pH of the reaction mixture to 7.3~7.5 with a . sodium bicarbonate solution, the reaction mixture was stirred for 4 hours at 70°C. After the mixture was cooled to room temperature, insoluble materials were filtered off, and the pH of the filtrate was adjusted to 4. After being concentrated under reduced pressure, the residue was chromatographed over silica gel. Elution with a 4 : 1 (v/v) mixture of acetonitrile/distilled water gave the above-indicated compound (150rag) in a pale yellow solid. m.P. : 194ºC~ (decomp.)

NMR : δ (D₂O + NaHCOa)

1.18(1, 2H), 1.44 (s, 6H), 1.50(m, 2H), 3.00(m, 1H), 3.41 (ABq, 2H), 4.32 (ABq, 2H) , 5.11 (d, 1H), 5.66(s, 1H), 5.71 (d. 1H),

6.92 (s, 1H).

MS(FAB. M + 1) : 650

TR(KBr, cm^-1) : 1768 (β-lactam), 1645, 1600. Example 51 : Synthesis of 7-[ (Z)-2-(2-aminothiazol-4-yl)-2-(2-carboxyprop -2-oxyimino)acetamido]-3-fl-(4-chlorophenyl)-4,6-diaminopyrimidinium-2-yl)thiomethyl-3-cephem-4-carboxylate 3-Acetoxymethyl-7-[(Z)-2-(2-aminothiazol-4-yl)-2-(2-carboxyprop-2-oxyimino)acetamido]-3-cephem-4-carboxylic acid (500mg) and 1-(4-chlorophenyl)-4,6-diamino-2(1H)-pyrimidinethione (200mg) were reacted in the same manner as described in Example 60 to give the above-indicated compound (170rag).

m.p. : 182ºC~(decomp.)

NMR : δ (D₂O + NaHCO₃)

1.43 (s, 6H), 3.42 (ABq, 2H) , 4.35 (ABq, 2H) , 5.08 (d, 1H), 5.64 (s. 1H), 5.66 (d, 1H), 6.84 (s, 1H), 7.26~7.62 (m, 4H).

HS(FAB. H + 1) : 720

IR(KBr. cm^-1) : 1768 (β-lactam), 1643, 1600.

Example 52 : Synthesis of 7-[(Z)-2-(2-aminothiazol-4-yl)-2-(2-carboxymethoxyimino)acetamidol-3-(4,6-diamino-1-phenylpyrimidinium-2- yl)thiomethyl-3-cephem-4-carboxylate 3-Acetoxymethyl-7-[(Z)-2-(2-aminothiazol-4-yl)-2-(2-carboxymethoxyimino) acetamido]-3-cephem-4-carboxylic acid (500mg) and 4,6-diaraino-1-phenyl-2(1H) -pyrimidinethione (200mg) were reacted in the same manner as described in Example 60 to give the above-indicated compound (190ng).

m.P. : 187°C~(decomp.)

NMR: δ (D₂O + NaHC0_s)

3.48 (ABq, 2H), 4.42 (ABq, 2H), 4.59 (s, 2H), 5.08 (d, 1H), 5.69 (s, 1H), 5.71 (d, 1H), 6.96 (s, 1H), 7.41~7.82 (m, 511). MS (FAB. H + 1) : 658

IR(KBr. cm^-1) : 1766 (β-lactam), 1655, 1600, 1538.

Example 53 : Synthesisof7-[(Z)-2-(2-aminothiazol-4-yl)-2-(1-carboxyeth

-1-oxyimino)acetamido]-3-(4,6-diamino-1-phenylpyrimidinium-2 -yl)thiomethyl-3-cephem-4-carboxylate

3-Acetoxymethyl-7-[(Z)-2-(2-aminothiazol-4-yl)-2-(2-carboxyeth-1-oxyimino)acetamido]-3-cephem-4-carboxylic acid (500mg) and 4,6-diamino-1-phenyl-2(1H)-pyrimidinethione (200mg) were reacted in the same manner as described in Example 60 to give the above-indicated compound (210mg). m.p. : 156ºC~(decomp.)

NMR : δ (D₂O + NaHC0₃)

1.48 (d, 3H), 3.48 (ABq, 2H), 4.49 (ABq, 2H), 5.16 (d, 1H) , 5.76 (s, 1H), 5.79 (d, 1H), 6.97 (s, 1H), 7.48~7.83 (m, 5H).

HS(FAB, H * 1) : 672

IR(KBr. cm^-1) : 1765 ( β-lactara), 1655, 1598, 1515.

Example 54 : Synthesis of 7-[(Z)-2-(2-aminothiazol-4-yl)-2-(ethoxyimino) acetamido]-3-(4,6-diamino-1-phenylpyrimidinium-2-yl)thiomethyl -3-cephem-4-carboxylate

3-Acetoxymethyl-7-[(Z)-2-(aminothiazol-4-yl)-2-(ethoxyimino)acetamido]-3-cephem-4-carboxylic acid (500mg) and 4,6-diamino-1-phenyl-2(1H)-pyrimidinethione (200mg) were reacted in the same manner as described in Example 50 to give the above-indicated compound (130rag).

m.P. : 182°C~(decomp.) NHR : δ (D₂O + NaHCO₃)

1.28 (t, 3H), 3.52 (ABq, 2H) , 4.20 (q. 2H), 4.31 (ABq, 2H) , 5.16 (d, 1H), 5.76 (s, 1H), 5.81 (d, 1H), 6.88 (s, 1H), 7.48~7.82 (m, 5H), MS(FAB, H + 1) : 628

IR(KBr. cm^-1) : 1768 (β-lactam), 1643, 1612, 1600, 1515.

Example 55 : Synthesis of 7-[(Z)-2-(2-arainothiazol-4-yl)-2-(ethoxyimino) acetamido]-3-[1-(4-chlorophenyl)-4,6-diamino-1-phenylpyrimidinium-2-yl)thiomethyl-3-cephem-4-carboxylate

3-Acetoxymethyl-7-[(Z)-2-(2-aminothiazol-4-yl)-2-(ethoxyimino)acetamido]-3-cephem-4-carboxylic acid (500mg) and 1-(4-chlorophenyl-4,6-diamino-2(1H)-pyrimidinethione (200mg) were reacted in the same manner as described in Example 60 to give the above-indicated compound (170mg).

m.P. : 177ºC~(decomp.)

NHR : δ (D₂O + acetone-do)

1.28 (t, 3H), 3.48 (ABq, 2H) , 4.21 (q, 2H) , 4.32 (ABq, 2H) , 5.12 (d, 1H), 5.73 (s, 1H), 5.80 (d, 1H), 6.87 (s, 1H), 7.52~7.79 (m, 4H). MS(FAB, M + 1) : 662

IR(KBr. cm^-1) : 1665 (β-lactam), 1643, 1610, 1530.

Example 56 : Synthesis of 7-[(Z)-2-(2-aminothiazol-4-yl)-2-(2-carboxyprop- 2-oxyimino)acetamido]-3-[4,6-diamino-1-(2,4-dimethylphenyl)- pyrimidinium-2-yl]thiomethyl-3-cephem-4-carboxylate

3-acetoxymethyl-7-[(Z)-2-(2-aminothiazol-4-yl)-2-(2-carboxyprop-2-oxyimino)acetamido]-3-cephem-4-carboxylic acid (500mg) and 4,6-diamino-1- (2,4-dimethylphenyl)-2(1H)-pyrimidinethione (200mg) were reacted in the same manner as described in Example 50 to give the above-indicated compound (180mg).

m.p. : 189ºC~ (decomp. )

NMR : δ (D₂O + NaHCO₃)

1.44 (s, 6H) , 2.02 (s, 3H) , 2.34 (s, 3H) , 3.36 (ABq, 2 H) . 4.27 (ABq, 2H) , δ.06 (d, 1H) , 5.68 (s, 1H) , 5.71 (d, 1H) , 6.88 (s, 1H) , 7.08~ 7.35 (m, 3H) .

MS(FAB. M + 1) : 714

IR(KBr. cm^{- 1}) : 1768 ( β-lactam) , 1641 , 1600, 1552.

Example 57 : Synthesis of 7-[ (Z)-2-(2-aminothiazol-4-yl)-2-(ethoxyimino) acetaraido]-3-[ (4,6-diamino-1-(2,4-dimethylphenyl)-pyrimidinium -2-yl ]thiomethyl-3-cephem-4-carboxylate

3-Acetoxymethyl-7-[(Z)-2-(2-aminothiazol-4-yl)-2-(ethoxyimino)acetamido]-3-cephem-4-carboxylic acid (500mg) and 4,6-diamino-1-(2,4-dimethylphenyl)-2(1H)-pyrimidinethione (200mg) were reacted in the same manaer as described in Example 60 to give the above-indicated compound (130mg). m.p. : 176'C~ (decomp.)

NMR : δ (D₂0 + acetone-dβ)

1.29 (t. 3H), 2.12 (s, 3H) , 2.40 (s, 3H) , 3.51 (ABq, 2H), 4.21(q, 2H), 4.36 (ABq, 2H), 5.09 (d, 1H), 5.76 (s, 1H), 5.81 (d, 1H), 6.90 (s, 1H), 7.23~7.41 (m, 3H).

MS(FAB. M + 1) : 656

IR(KBr. cm^-1) : 1770 (β''lactam), 1643, 1610, 1540. Example 58 : Synthesis of 7-[(Z)-2-(2-aminothiazol-4-yl)-2-(2-carboxyprop -2-oxyimino)acetamido]-3-[4,6-diamino-1-(2,6-dimethoxyphenyl) -pyrimidiniura-2-yl]thiomethyl-3-cephem-4-carboxylate 3-Acetoxyιethyl-7-[(Z)-2-(2-aminothiazol-4-yl)-2-(2-carboχyprop-2-oxyimino)acetamido]-3-cephem-4-carboxylic acid (500mg) and 4,6-diamino-1-(2, 6-dimethoxyphenyl)-2(1H)-pyrimidinethione (200mg) were reacted in the same manner as described in Example 50 to give the above-indicated compound (210mg).

m.p. : 164ºC~(decomp.)

NMR : δ (D₂O + NaHCO₃)

1.46 (s, 6H), 3.40 (ABq, 2H) , 3.79 (s, 611), 4.29 (ABq, 211), 5.12 (d, 1H), 5.67 (s, 1H), 5.76 (ri, 1H), 6.95 (s, 1H), 7.04~7.28 (m, 311). HS(FAB. H + 1) : 746

IR(KBr, cm^-1) : 1766 (β-lactam), 1641, 1600, 1550.

Example 59 : Synthesis of 7-[(Z)-2-(2-aminothiazol-4-yl)-2-(2-carboxyprop

-2-oxyimino)acetamido]-3-[(4,6-diamino-1-(4-hydroxyphenyl)- pyrimidinium-2-y1]thiomethyl-3-cephem-4-carboxylate

3-Acetoxymethyl-7-{(Z)-2-(2-aminothiazol-4-yl)-2-(2-carboxyprop-2-oxyimino)acetaraidol-3-cephem-4-carboxylic acid (500mg) and 4,6-diamino-1-(4- hydroxyphenyl)-2(1H)-pyrimidinethione (200mg) were reacted in the same manner as described in Example 50 to give the above-indicated compound (230mg) .

m.p. : 171°C~(decomp.)

NMR : δ (D₂O + NaHCO₃) 1.47 (s, 6H), 3.39 (ABq, 2H) , 4.27 (ABq, 2H) , 5.06 (d, 1H), 5.64 (s, 1H), 5.74 (d, 1H), 6.91 (s, 1H), 6.90~7.32 (m, 4H),

MS(FAB. M + 1) : 702

IR(KBr. cm^-1) : 1768 (β-lactam), 1641, 1600, 1525.

Claims (1)

1. What is claimed is;

   1. A cephalosporin compound of the formula

   wherein

   R¹ is a C_1~4 alkyl, C_3~4 alkenyl, C_3~4 alkynyl group, or

   -C(R^a)(R^b)CO₂H, wherein R^a and R^b are the same or different, and each is a hydrogen atom or a C_1~4 alkyl group, or R^a and R^b form a C_3~7 cycloalkyl group with the carbon atom to which they are linked ;

   R² is aC_1~4 alkyl, C_3~4 alkenyl or C_3~4 cycloalkyl group, a substituted or unsubstituted amino group, or a substituted or unsubstituted phenyl group ;

   R³ is hydrogen or a C_1~4 alkyl group ; and

   Q is N or CH ;

   or a pharmacuetically acceptable non-toxic salt thereof, or a physiologically hydrolyzable ester or solvate thereof.

   2. The compound according to Claim 1 which is 7-[(Z)-2-(2-aminothiazol- 4-yl)-2-(2-carboxylprop-2-oxyimino)acetamido]-3-(4,6-diaraino-1- methylpyriιidiniura-2-yl)thiomethyl-3-cephem-4-carboxylate.

   3. The compound according to Claim 1 which is 7-[(Z)-2-(2-aminothiazol- 4-yl)-2-(2-carboxylprop-2-oxyimino)acetaιino]-3-(4,β-diamino-1- ethylpyrimidiniuι-2-yl)thiomethyl-3-cephem-4-carboxylate. 4. The compound according to Claim 1 which is 3-(1-allyl-4,6- diaminopyrimidinium-2-yl)thiomethyl-7-[(Z)-2-(2-aminothiazol-4-yl)-2-(2- carboxyprop-2-oxyimino)acetaιido]-3-cephem-4-carboxylate.

   5. The compound according to Claim 1 which is 7-[(Z)-2-(2-aminothiazol- 4-yl)-2-(1-carboxyeth-1-oxyimino)acetamido]-3-(4,6-diamino-1- methylpyriιidinium-2-yl)thiomethyl-3-cephem-4-carboxylate.

   6. The compound according to Claim 1 which is 7-[(Z)-2-(2-aminothiazol- 4-yl)-2-(1-carboxyeth-1-oxyiιino)acetaιido]-3-(4,6-diaιino-1- ethylpyrimidiniuι-2-yl)thioιethyl-3-cephem-4-carboxylate.

   7. The compound according to Claim 1 which is 3-(1-allyl-4,6- diaminopyriιidiniuι-2-yl)thioιethyl-7-[(Z)-2-(2-aιinothiazol-4-yl)-2-(1- carboxyeth-1-oxyiιino)acetamido]-3-cepheι-4-carboxylate.

   8. The compound according to Claim 1 which is 7-[(Z)-2-(2-aιinothiazol- 4-yl)-2-(carboxyιethoxyimino)acetaιido]-3-(4,6-diamino-1- methylpyrimidinium-2-yl)thiomethyl-3-cephem-4-carboxylate. 9. The compound according to Claim 1 which is 7-[(Z)-2-(2-aminothiazol- 4-yl)-2-(carboxyιethoxyimino)acetanido]-3-(4,6-diamino-1-ethylpyrimidinium- 2-yl)thiomethyl-3-cephem-4-carboxylate.

   10. The compound according to Claim 1 which is 3-(1-allyl-4,6- diaminopyrimidinium-2-yl)thioιethyl-7-[(Z)-2-aminothiazol-4-yl)-2- (carboxyιethoxyimino)acetaιido]-3-cephem-4-carboxylate. 11. The compound according to Claim 1 which is 7-[(Z)-2-(2-aminothiazol- 4-yl)-2-(methoxyiιino)acetaaido]-3-(4,6-diaιino-1-methylpyrimidinium-2-yl) thiomethyl-3-cephem-4-carboxylate.

   12. The compound according to Claim 1 which is 7-[(Z)-2-(2-aminothiazol- 4-yl)-2-(ethoxyimino)acetamido]-3-(4,6-diamino-1-methylpyrimidinium-2-yl) thiomethyl-3-cephem-4-carboxylate.

   13. The compound according to Claim 1 which is 7-[(Z)-2-(2-aminothiazol- 4-yl)-2-(ethoxyimino)acetamido]-3-(4,6-diamino-1-ethylpyrimidinium-2-yl) thiomethyl-3-cephem-4-carboxylate.

   14. The compound according to Claim 1 which is 7-[(Z)-2-(5-amino-1,2,4- thiadiazol-3-yl)-2-(2-carboxyprop-2-oxyimino)acetamido]-3-(1,4,6- triaιinopyrimidinium-2-yl)thioιethyl-3-cephem-4-carboxylate.

   15. The compound according to Claim 1 which is 7-[(Z)-2-(2-aminothiazol- 4-yl)-2-(1-carboxyeth-1-oxyimino)acetamido]-3-(1,4,6-triaminopyrimidinium- 2-yl)thiomethyl-3-cephem-4-carboxylate. 16. The compound according to Claim 1 which is 7-[(Z)-2-(2-aminothiazol- 4-yl)-2-(2-carboxyprop-2-oxyimino)acetamido]-3-(1,4,6-triaminopyrimidinium- 2-yl)thiomethyl-3-cephem-4-carboxylate.

   17. The compound according to Claim 1 which is 7-[(Z)-2-(2-aminothiazol- 4-yl)-2-(ethoxyimino)acetamido]-3-(1,4,6-triaminopyrimidinium-2-yl) thioιethyl-3-cepheι-4-carboxylate. 18. The compound according to Claim 1 which is 7-[(Z)-2-(5-amino-1,2,4- thiadiazol-3-yl)-2-(ethoxyimino)acetamido]-3-(1,4,6-triaminopyrimidinium- 2-yl)thiomethyl-3-cephem-4-carboxylate.

   19. The compound according to Claim 1 which is 7-[(Z)-2-(2-aminothiazol- 4-yl)-2-(2-proρyn-1-oxyiιino)acetamido]-3-(1,4,6-triaminopyrimidinium-2- yl)thiomethyl-3-cephem-4-carboxylate.

   20. The compound according to Claim 1 which is 7-[(Z)-2-(2-aminothiazol- 4-yl)-2-(ιethoxyimino)acetamido]-3-(l,4,6-triaιinopyrimidinium-2-yl) thiomethyl-3-cephem-4-carboxylate.

   21. The compound according to Claim 1 which is 7-[(Z)-2-(5~amino-1,2,4- thiadiazol-3-yl)-2-(ethoxyimino)acetamido]-3-(4,6-diaιino-1- methylpyrimidinium-2-yl)thiomethyl-3-cephera-4-carboxylate. 22. The compound according to Claim 1 which is 7-[(Z)-2-(5-amino-1,2,4- thiadiazol-3-yl)-2-(ethoxyimino)acetamido]-3-(4,6-diaιino-1- ethylpyrimidinium-2-yl)thiomethyl-3-cephem-4-carboxylate.

   23. The compound according to Claim 1 which is 7-[(Z)-2-(5-amino-1,2,4- thiadiazol-3-yl)-2-(ethoxyimino)acetamido1-3-(4,6-diamino-1- propylpyrimidinium-2-yl)thiomethyl-3-cephem-4-carboxylate.

   24. The compound according to Claim 1 which is 3-(1-allyl-4,6- diaminopyrimidiniuι-2-yl)-7-[(Z)-2-(5-amino-1,2,4-thiadiazol-3-y1)-2- (ethoxyimino)acetamido]-3-cephem-4-carboxylate. 25. The compound according to Claim 1 which is 7-[(Z)-2-(5-amino-1,2,4- thiadiazol-3-y1)-2-(methoxyimino)acetamido]-3-(4,6-diamino-1- methylpyriιidinium-2-yl)thiomethyl-3-cephem-4-carboxylate.

   26. The compound according to Claim 1 which is 7-[(Z)-2-(5-armino-1,2,4- thiadiazol-3-yl)-2-(methoxyimino)acetamido]-3-(4,6-diamino-1- ethylpyrimidinium-2-yl)thiomethyl-3-cephem-4-carboxylate.

   27. The compound according to Claim 1 which is 7-[(Z)-2-(5-amino-1,2,4- thiadiazol-3-yl)-2-(2-carboxyprop-2-oxymino)acetamido]-3-(4,6-diamino-1- methylpyriιidinium-2-yl)thiomethyl-3-cephem-4-carboxylate.

   28. The compound according to Claim 1 which is 7-[(Z)-2-(5-araino-1,2,4- thiadiazol-3-yl)-2-(2-carboxyprop-2-oxyimino)acetamido]-3-(4,6-diamino- l-ethylpyriιidinium-2-yl)thiomethyl-3-cephem-4-carboxylate.

   29. The compound according to Claim 1 which is 7-[(Z)-2-(5-amino-1,2,4- thiadiazol-3-yl)-2-(2-carboxyprop-2-oxyimino)acetamido]-3-(4,6-diamino- l-propylpyriιidinium-2-yl)thiomethyl-3-cephem-4-carboxylate. 30. The compound according to Claim 1 which is 7-[(Z)-2-(5-amino-1,2,4- thiadiazol-3-yl)-2-(2-carboxyprop-2-oxyimino)acetamido]-3-(l-butyl-4,6- diaminopyrimidinium-2-yl)thiomethyl-3-cephem-4-carboxylate.

   31. The compound according to Claim 1 which is 7-[(Z)-2-(2-aminothiazol- 4-yl)-2-(2-carboxyprop-2-oxyimino)acetamido]-3-(4,6-diamino-1,5- diιethylpyriιidinium-2-yl)thiomethyl-3-cephem-4-carboxylate. 32. The compound according to Claim 1 which is 7-[(Z)-2-(2-aminothiazol- 4-yl)-2-(2-carboxyprop-2-oxyimino)acetamido]-3-(4,6-diamino-5-ethyl-1- methylpyrimidinium-2-yl)thiomethyl-3-cephem-4-carboxylate.

   33. The compound according to Claim 1 which is 7-[(Z)-2-(2-aminothiazol- 4-yl)-2-(2-carboxyprop-2-oxyimino)acetamido]-3-(4,6-diamino-1-ethyl-5- methylpyrimidinium-2-yl)thiomethyl-3-cephem-4-carboxylate.

   34. The compound according to Claim 1 which is 7-[(Z)-2-(2-aminothiazol- 4-yl)-2-(2-carboxyprop-2-oxyimino)acetamido]-3-(4,6-diamino-1,5- diethylpyrimidinium-2-yl)thiomethyl-3-cephem-4-carboxylate.

   35. The compound according to Claim 1 which is 7-[(Z)-2-(2-aminothiazol- 4-yl)-2-(2-carboxyprop-2-oxyimino)acetamino]-3-(5-methyl-1,4,6- triaminopyrimidinium-2-yl)thiomethyl-3-cephem-4-carboxylate.

   36. The compound according to Claim 1 which is 7-[ (Z)-2-(2-aminothiazol- 4-yl)-2-(2-carboxyprop-2-oxyimino)acetamido]-3-(4,6-diamino-1- phenylpyrimidiniura-2-yl)thiomethyl-3-cephem-4-carboxylate. 37. The compound according to Claim 1 which is 7-[ (Z)-2-(2-aminothiazol- 4-yl)-2-(2-carboxyprop-2-oxyimino)acetamido]-3-[1-(4-hydroxyphenyl)-4,6- diaminopyrimidinium-2-yl]-thiomethyl-3-cephem-4-carboxylate.

   38. The compound according to Claim 1 which is 7-[(Z)-2-(2-aminothiazol- 4-yl)-2-(carboxyιethoxyiιino)acetamido]-3-(4,6-diamino-1- phenylpyrimidinium-2-yl)thiomethyl-3-cephem-4-carboxylate. 39. The compound according to Claim 1 which is 7-[(Z)-2-(2-aminothiazol- 4-yl)-2-(1-carboxyeth-1-oxyimino)acetamido]-3-(4,6-diamino-1- phenylpyrimidinium-2-yl)thiomethyl-3-cephem-4-carboxylate.

   40. The compound according to Claim 1 which is 7-[(Z)-2-(2-aminothiazol- 4-yl)-2-(ethoxyimino)acetaιido]-3-(4,β-diamino-1-phenylpyriιidinium-2-yl) thiomethyl-3-cephem-4-carboxylate.

   41. The compound according to Claim 1 which is 7-[(Z)-2-(2-arainothiazol- 4-yl)-2-(ethoxyimino)acetamido]-3-[1-(4-chlorophenyl)-4,6- diaminopyriιidinium-2-yl]thiomethyl-3-cephem-4-carboxylate.

   42. The compound according to Claim 1 which is 7-[(Z)-2-(2-a*inothiazol- 4-yl)-2-(2-carboxyprop-2-oxyimino)acetamido]-3-[4,6-diamino-1-(2,4- dimethylphenyl)-pyrimidiniura-2-yl]thiomethyl-3-cephem-4-carboxylate.

   43. The compound according to Claim 1 which is 7-[(Z)-2-(2-aminothiazol- 4-yl)-2-(ethoxyimino)acetamido]-3-(4,6-diamino-1-(2,4-dimethylphenyl)- pyrimidinium-2-yl]thiomethyl-3-cephem-4-carboxylate. 44. The compound according to Claim 1 which is 7-[(Z)-2-(2-aminothiazol- 4-y1)-2-(2-carboxyprop-2-oxyimino)acetamido]-3-[4,6-diaιino-1-(2,6- dimethoxyphenyl)-pyriιidinium-2-yl]thioιethyl-3-cephem-4-carboxylate.

   45. The compound according to Claim 1 which is 7-[(Z)-2-(2-aminothiazol- 4-yl)-2-(2-carboxyprop-2-oxyimino)acetamido]-3-[4,6-diamino-1-(4- chlorophenyl)-pyrimidinium-2-yl]thiomethyl-3-cephera-4-carboxylate. 46. The compound according to Claim 1 which is 7-[(Z)-2-(2-aminothiazol- 4-yl)-2-(1-carboxyeth-1-oxyimino)acetamido]-3-[4,6-diamino-1- propylpyrimidinium-2-yl]thiomethyl-3-cephem-4-carboxylate .

   47. The compound according to Claim 1 which is 7-[(Z)-2-(2-aminothiazol- 4-yl)-2-(2-propyn-1-oxyimino)acetamido]-3-(4,6-diamino-1- methylpyrimidinium-2-yl)thiomethyl-3-cephem-4-carboxylate.

   48. The compound according to Claim 1 which is 7-[(Z)-2-(2-aminothiazol- 4-yl)-2-(2-propyn-1-oxyimino)acetamido]-3-(4,6-diamino-1- ethylpyrimidinium-2-yl)thiomethyl-3-cephem-4-carboxylate.

   49. The compound according to Claim 1 which is 7-[(Z)-2-(2-aminothiazol- 4-yl)-2-(2-carboxyprop-2-oxyimino)acetamido]-3-(1-cyclopropyl-4,6- diaminopyrimidinium-2-yl)-3-cephem-4-carboxylate.

   50. The compound according to Claim 1 which is 7-[(Z)-2-(2-aminothiazol- 4-yl)-2-(2-propen-1-oxyimino)acetamido]-3-(4,6-diamino-1- methylpyrimidinium-2-yl)-3-cephem-4-carboxylate. 51. The compound according to Claim 1 which is 7-f(Z)-2-(2-aminothiazol- 4-yl)-2-(2-propen-1-oxyimino)acetamido]-3-(4,6-diamino-1- ethylpyrimidinium-2-yl)-3-cephem-4-carboxylate.

   52. A process for preparing the cephalosporin compounds of formula(I), pharmaceutically acceptable non-toxic salts thereof, or physiologically hydrolyzable esters or solvates thereof, which comprises reacting the compounds of the formula(II) with the compounds of the formula(III) in the presence of a solvent

   wherein

   R¹, R², R³ and Q are the same as defined in Claim 1 ;

   n is an integer of 0 or 1 ;

   R⁴ is a hydrogen atom or an amino protecting group ;

   R^B is a C_1~4 alkyl, C_3~4 alkenyl or C_3~4 alkynyl group, or -C(R^a)(R^b)CO₂(R^c), wherein R^a and R^b are the same or different, and each is a hydrogen atom or a C_1~4 alkyl group, or R^a and R^b form a C_3~7 cycloalkyl group with the carbon atom to which they are linked ; and R^c is a hydrogen atom or a carboxyl protecting group ; R³ is a hydrogen or a carboxyl protecting group ; and

   L is a leaving group.

   53. The process according to Claim 52 wherein the solvent is water, or a lixed solvent of water and a water-mixable solvent.

   54. The process according to Claim 63 wherein the water-mixable solvent is acetonitrile or acetone. 65. The process according to Claim 52 wherein the solvent has a pH of from 5 to 8.

   56. The process according to Claim 52 wherein the compounds(II) are used in an amount of from 1 to 2 equivalent(s) based on 1 equivalent of the compounds(III).

   57. The process according to Claim 52 which is carried out in the presence of one or more stabilizing agents.

   58. The process according to Claim 57 wherein the stabilizing agent is sleeted from the group consisting of sodium iodide, potassium iodide, sodium bromide, potassium bromide and potassium thiocyanate.

   59. The process according to Claim 52 which further comprises removing the amino protecting group and/or the carboxyl protecting group and/ or reducing the S-oxide, before or after reacting the compounds(II) and the compounds(III).

   60. A pharmaceutical composition which comprises a therapeutically effective amount of one or lore the cephalosporin compounds of formula(I) recited in Claim 1, pharmaceutically acceptable non-toxic slats thereof, or physiologically hydrolyzable esters or solvates thereof as active ingredients, in assoication with pharmaceutically acceptable carriers, excipients or other additives therefor.