KR900002673B1 - Intermediate derivation for monosulfactams and their preparation - Google Patents

Abstract

A beta-lactams for formula (I) and their pharmaceutically acceptable salts are prepared. A specific cpd. is (3S(Z)-2-(((1-(2-amino-4- thiazolyl)-2-((4,4-dimethyl-2-oxo-1-(sulphooxy)-3azetidinyl)amino)2- 2oxaethylidene)amino)oxy)-pro-penoic acid. A method of prepn. comprises reacting a cpd. of formula H2N-O-C (:CR3R4)-COOA1[A1= carboxyl-protecting gp. with a 2-amino-4thiazolylglyoxylic acid of formula (II) [A2= H or amino-protecting gp. . In the formulas, R1 and R2 are each H or alkyl or R1 and R2 are (CH2)n (in which n is 4-6); R3 and R4 are each H or C1-3 alkyl.

Description

Monosulpactam Intermediates for Production and Process for the Preparation thereof

The present invention relates to compounds having antibacterial activity and pharmacologically acceptable salts thereof, represented by the following structural formula (I).

Symbols described in the above formula (I) and throughout the present specification are defined as follows.

R ₁ and R ₂ are the same or different from each other and are each hydrogen or an alkyl group, or R ₁ and R ₂ together are — (CH ₂ ) _n — where n is 2, 3, 4, 5 or 6 R ₃ and R ₄ , which are the same as or different from each other, are each hydrogen or an alkyl group having 1 to 3 carbon atoms.

The term "alkyl" is a straight and branched chain group unless otherwise defined. As such groups, groups having 1 to 10 carbon atoms are suitable.

Compounds according to the invention together with inorganic and organic bases form basic salts, which salts fall within the scope of the invention. Such salts include ammonium salts, alkali metal salts, alkaline earth metal salts and salts with organic bases such as dicyclonuxylamine, benzatin, N-metal-di-glucamine, hydramine and the like.

The compounds of the present invention are represented by acids. However, they also exist as zwitterions (internal salts) and are also included in "pharmacologically acceptable salts" and are included within the scope of the present invention.

Β-lactams of the formula (I) and pharmacologically acceptable salts thereof have activity against gram positive and gram negative bacteria. The compounds of the present invention are used in the treatment of bacterial infections (including urinary tract infections and respiratory infections) in mammals such as livestock (dogs, cats, cattle, horses, etc.) and humans.

To treat mammalian bacterial infections, the compounds of the present invention were administered at a dose of about 1.4-300 mg / kg / day, suitably about 14-100 mg / kg / day, to a mammal animal in need thereof. In order to use the β-lactam according to the present invention, all the administration modes conventionally used for infection delivery of penicillin and cephalosporin were used, for example, oral, intravenous, intramuscular administration and suppository administration.

The compound according to the present invention is represented by the following structural formula (II)

Wherein A ₁ is a carboxyl protecting group. Carboxyl protecting groups are known in the art and are used to prevent carboxyl groups from participating in the following reactions. Examples of groups used to protect carboxyl groups are described in US Pat. No. 4,144,333, filed March 13, 1979. As the protecting group, t-butyl, diphenylmethyl and phenylmethyl groups are suitable. Carboxylic protecting groups can be removed using methods well known in the art that vary depending on the particular protecting group. For example, when the protecting group is a t-butyl group, it can be removed using trifluoroacetic acid, dichloromethane and anisole, or using trifluoroacetic acid and thioanisole. If the protecting group is a phenylmethyl group, it uses trifluoroacetic acid and thioanisole, or trimethylsilyliodide and an acid scanbinder, for example N-methyl-N- (trimethylsilyl) trifluoroacetamide Can be removed. If the protecting group is a diphenylmethyl group, it uses trifluoroacetic acid, dichloromethane and anisole, or trimethylsilylodide and acid scavenger, for example N-methyl-N- (trimethylsilyl) trifluor Loacetamide can be used to remove. Compounds of formula II are novel and form an important part of the present invention.

The compound of formula (II) is reacted with 2-amino-4-thiazolylglyoxylic acid (or a derivative thereof protected with an amino group) to give the following formula (III)

In the formula, A ₂ was hydrogen or an amino protecting group. Amino protecting groups are well known in the art and they are used to prevent the amino groups from participating in the following reactions. Examples of amino protecting groups include aromatic acyl groups (e.g. p-nitrobenzyl and p-tert-butylbenzoyl groups), aliphatic acyl groups (e.g. formyl, acetyl, propionyl, monochloroacetyl, dichloroacetyl, trochloroacetyl And trifluoroacetyl groups), esterified carboxyl groups (eg methoxycarbonyl, ethoxycarbonyl, t-butoxycarbonyl, isopropoxycarbonyl, 2-cyanoethoxycarbonyl, β, β, β-trochloroethoxycarbonyl, benzyloxycarbonyl, p-nitrobenzyloxycarbonyl, p-methoxybenzyloxycarbonyl, diphenylmethyloxycarbonyl, methoxymethyloxycarbonyl, acetylmethyloxy Carbonyl, isobornyloxycarbonyl and phenyloxycarbonyl groups), methylene groups [eg, (hexahydro-1H-azin-1-yl) methylene groups], sulfonyl groups (eg 2-amino-2-carboxyethyl Sulfonyl groups) and amino-protecting groups other than acyl groups (eg, trityl, 2-nitrophenylthio, - or a trialkyl silyl, benzyl and P- nitrobenzyl group). The carboxylic acid of the above formula (III) is a novel compound, which is an important part of the present invention.

The carboxylic acid of the structural formula (III) is represented by the following structural formula (IV)

By coupling with β-lactam of Structural Formula (Ⅴ)

The corresponding compound represented by is obtained. The reaction proceeded very easily when the carboxylic acid was active. Active forms of carboxylic acids are well known in the art and examples include acid halides, acid anhydrides (including mixed anhydrides), active acid amides and active acid esters. From the compound of the above formula (V), the protecting group was removed using a method known in the art to obtain the corresponding product of the formula (I).

As a next method, the compound of formula (II)

By reacting with glyoxylic acid of, the corresponding compound of formula (V) can be obtained, and the protecting group can be removed from the compound to obtain the corresponding product of formula (I).

As another method, the compound of formula (I) is removed from the compound of formula (II) by using a method known in the art to remove the protecting group

It can be prepared by obtaining a product of. The compounds of formula (VII) are novel and these compounds form an important part of the present invention.

The compound of formula (VII) was reacted with the compound of formula (VI), and optionally the protecting group was removed to obtain a compound of formula (I).

Β-lactam of structural formula (IV) is a structural formula (VII)

In the formula, A ₃ is an amino protecting group, preferably t-butoxycarbonyl or benzyloxycarbonyl group.

A ₄ -O-NH ₂ (Ⅸ)

(Wherein A ₄ is a protecting group such as benzyl, trityl or pivaloyl group) by coupling with O-protective hydroxylamine represented by the following structural formula

It can be prepared by obtaining the corresponding compound represented by. The reactant coupling agent, for example 1-ethyl-3 (dimethylaminopropyl) carbodiimide, dicyclohexylcarbodiimide or dicyclohexylcarbodiimide N-hydroxybenzotriazole was carried out in the presence.

The compound of formula (VII) is represented by the following structural formula (VII)

Wherein m is 0, 1, 2 or 3, and reacts with a pyridine (optionally substituted) -sulfur trioxide complex to give the following structural formula (XII)

The corresponding compound of was obtained. The sulfonation reaction can be carried out in an organic solvent such as pyridine, mono-, di- or trimethylpyridine, dichloromethane, 1,2-dichloroethane, acetonitrile, dimethylformamide or dioxane.

The compound of formula (XII) was cyclized by treating with a base to give the following formula (XIII)

The corresponding compound of was obtained. The base is suitably an inorganic base, for example alkyllimetal carbonate, and the reaction is carried out in a mixture of water and an organic solvent (e.g. ethyl acetate, methyl butyl ketone, pyridine or mono-, di- or trimethylpyridine). Can be.

From the compound of formula (XIII), protecting group A ₄ is removed using a technique known in the art, and the following structural formula (XIV)

The corresponding compound of was obtained. For example, when A ₄ is a benzyl group, protecting group removal can be accomplished by catalytic hydrogenation. In the case of A0 ₊ pivaloyl group, protecting group removal can be achieved by treatment with a base such as sodium sulfide or sodium hydroxide. When A ₄ is a triti group, protecting group removal can be achieved by treatment with an aqueous 80% acetic acid solution.

The compound of formula (VII) was treated with pyridine (optionally substituted) -sulfur trioxide complex of formula (XI) to give the following formula (VII)

The pyridinium salt of the corresponding compound of was obtained. The reaction can be carried out in a solvent such as pyridine (optionally substituted), dichloromethane or 1,2-dichloroethane. Conventional techniques (eg, ion-exchange resins) can be used to convert the pyridinium salts formed above to other salts and free acids.

The compound of formula (IV) wherein A ₂ is hydrogen can be obtained by removing the protecting group of the corresponding compound of formula (VIIV). The protecting group removal method used depends on the specific protecting group. For example, when the protecting group is a t-butoxycarbonyl group, trifluoroacetic acid can be used to remove the amino-protecting group. When the protecting group is a benzyloxycarbonyl group, a catalytic hydrogenation reaction can be used.

In addition, β-lactam of structural formula (IV) can be manufactured using the method of US Pat. No. 4,337,197 which was patented on June 29, 1982. In addition, the compounds of formula (VI) can be prepared using the acylation techniques described in the patent.

The amino acids of the structural formulas are known or can be readily obtained using methods known in the art.

[See, eg, J. Org. Chem., 44, page 3967 (1979), J. Org. Chem., 46, page 2809 (1981), Z. Chem., 10. , 393 pages (1970), Tetrahedron, 39, 2085 (1983), Liebigs Annalen der Chem., 763, page 1 (1972), Synthesis, page 216 (1979) ), Bull. Chem. Soc. Japan, 39, 2287 (1966)]. The methods are the reaction of the protected glycine (both amino and carboxyl groups protected) with a suitable ketone (scan) (aldol condensation) followed by removal of the carboxyl protecting group.

A compound of formula (II) wherein "A ₁ " is a t-butyl group and R ₃ and R ₄ are each hydrogen is the following formula (XVI)

Compounds of can be prepared by treating with hydrazine or methylhydrazine. Compounds of formula (XVI) wherein A ₁ is a t-butyl group are known (see Belgium Patent 866,422). By a method known in the art, the t-butyl group is removed and di; It may be substituted with a replacement protecting group such as phenylmethyl or phenethyl group.

The compound of formula (II) is represented by the following formula (X ')

It can be prepared from ketones or aldehydes. The compound of formula (XVII) is reacted with α-haloacetate ester (eg, ethyl chloroacetate) in the presence of a strong base such as potassium t-butoxide, and the resulting glycidic ester is hydrolyzed [J. Org. Chem. 26, page 3176 (1961)]

The salt of the corresponding compound represented by is obtained.

As another method, the compound of structural formula (X ') is represented by the following structural formula (X')

The salts of the compounds can be prepared by treatment with aqueous hydrogen peroxide solution in the presence of a sodium tungstate catalyst (see J. Org. Chem., 50, page 1979 (1985)).

The compound of formula (XVII) is prepared in the presence of a base (e.g. alkali metal hydroxide) in a solvent (e.g. water, water / dioxane, water / dimethylsulfoxide, water / ethanol, ethanol, dimethylformamide or dimethyl sulfoxide) Treated with acetone oxime, benzaldehyde oxime, p-methoxybenzaldehyde oxime or t-butyl N-hydroxycarbamate, the following structural formula (XX)

Wherein A ₅ is isopropylidene, benzylidene or p-methoxy benzylidene, or "A ₅ = N-" is a t-butoxycarbonylamino group. When A ₅ is an isopropylidene, benzylidene or p-methoxybenzylidene group, the compound of formula (XX) is removed with a mineral acid in the presence of water to remove the protecting group, which is replaced by a technique known in the art. Can be converted into a compound having a replacement protecting group (ie, A ₅ is a phthaloyl group or “A ₅ = N” group is a t-butoxycarbonylamino group). When "A ₅ = N-" is a t-butoxycarbonylamino group, converting the compound of formula (XX) to a compound having a replacement protecting group uses trifluoroacetic acid and anisole to remove the protecting group, which It can be accomplished by substitution with a replacement protecting group by techniques known in the art.

A compound of formula (XX) (or a compound corresponding to this having a different protecting group) is esterified using a carboxyl protecting group A ₁ to give the following formula (XXI)

The corresponding compound of was obtained.

Compounds of formula (XXI) are dehydrated using any one of a number of techniques known in the art to provide formula (XXII)

The corresponding compound of was obtained. For example, dehydration can be achieved by treating the compound of formula (XXI) with methanesulfonyl chloride in the presence of at least 2 equivalents of triethylamine. Alternatively, the compound of formula (XXI) is treated with methanesulfonyl chloride in the presence of at least one equivalent of triethylamine, then the corresponding mesylate is isolated and finally an inorganic base in an organic solvent such as dimethylformamide. (Example: potassium carbonate) to remove the compound to obtain a compound of formula (XXII). Alternatively, compounds of formula (XXI) were converted to compounds of formula (XXII) using reagents such as thionyl chloride / pyridine, phosgene / pyridine or diethylaminosulfurtrifluoride / pyridine.

The protecting group was selectively removed from the compound of formula (XXII) using techniques known in the art to obtain the target compound of formula (II). Alternatively, protecting group removal techniques known in the art may be used to convert the compound of formula (XXII) to the corresponding compound of formula (VII).

In the above synthesis method for preparing a compound of formula (II) or (III), R ₄ is a cis of the carboxyl moiety from the compound of formula (X ′) wherein R ₄ is in the trans position relative to the carboxyl moiety. It is possible to produce compounds of general formula (I) in position.

As another method, the following structural formula (XXIII)

From the amino acids of, a compound of formula (II) or formula (VII) wherein one of R ₃ and R ₄ is hydrogen and the other is an alkyl group having 1 to 3 carbon atoms can be prepared.

The compound of formula (XXIII) was converted to the corresponding benzyl ether using a conventional method, to give the following formula (XXIV)

Was obtained.

The compound of formula (XXIV) is reacted with nitrous acid in the presence of bromine ions to give formula (XXV)

The corresponding compound of was obtained.

According to a conventional method, the compound of formula (XXV) is esterified using t-butyl group to give formula (XXVI)

The corresponding compound of was obtained.

The compound of formula (XXVI) is reacted with N-hydroxyphthalimide in dimethylformamide in the presence of a base such as potassium carbonate to give the following formula (XX ')

Was obtained.

This was hydrolyzed to remove the benzyl protecting group, followed by dehydration to give the following structural formula (XX ')

Was obtained.

By a method known in the art, the T-butyl group of the compound of the structural formula (XX ') is substituted with a diphenylmethyl group and a replacement protecting group, and the following structural formula (XX')

Was obtained.

The compound of formula (XX ') was treated with hydrazine or methylhydrazine to obtain the corresponding compound of formula (II) wherein A ₁ is a diphenylmethyl group. Standard protecting group removal and protecting group introduction methods were used to convert this compound to other compounds of formulas (II) and (VII).

As another method, the compound of formula (XXVI) is treated with t-butyl-N-hydroxycarbamate in a solvent such as dimethyl formamide in the presence of a base such as sodium hydride to give the following formula (XXX)

Can be converted to the corresponding compound.

The benzyl protecting group is removed from the compound of formula (XXX) by hydrogenolysis, and then dehydrated to give structure (XXXI).

Was obtained. Using standard protecting group removal and protecting group introduction methods, compounds of formula (XXXI) can be converted into compounds of formula (II), which can be readily converted to the corresponding compounds of formula (VII).

Using this method, the following geometrical formula (XXXII)

From the compound having the following structural formula (XXXⅢ)

A compound having

As another method, the following structural formula (XXXIV)

Wherein one of R ₃ and R ₄ is hydrogen and the other is an alkyl group having from 1 to 3 carbon atoms, is used in the preparation of the compound of formula (XVI) and is described in Belgian Patent No. 866,422 It can be converted to the compound of formula (XX ') by a method similar to that described.

R ₄ a is a compound having the geometry of the structural formula (XXXⅣ) in the cis position relative to the carboxyl group, R ₄ was converted to compound of formula (XXXⅢ) in the cis position relative to the carboxyl group.

기를 가지며, R₃및 R₄가 상이할 경우, syn 또는 anti 이성질체로 존재하거나, 또는 이들 이성질체들의 혼합물로 존재한다. 이러한 이성질체들 모두가 본 발명의 범위 안에 포함된다.The compound of formula (I) has at least one chiral central carbon atom (at the 3-position of the β-lactam nucleus) to which an amino or acylamino substituent is attached. The present invention relates to such β-lactams wherein the stereochemistry at the 3-position chiral center of the β-lactam nucleus is identical to the arrangement at the 6-position carbon atom of natural penicillin (eg penicillin G). Compound of formula (I)

Group, and when R ₃ and R ₄ are different, exist as syn or anti isomers, or as mixtures of these isomers. All such isomers are included within the scope of the present invention.

을 가지며, 그리하여, syn 또는 anti 이성질체로 존재하거나, 또는 이들 이성질체들의 혼합물로 존재한다. 이러한 이성질체 형태 모두가 본 발명의 범위 안에 포함된다. 그러나, 일반적으로, 구조식(I)의 화합물의 syn이성질체가 가장 큰 활성을 갖는다.Compound of formula (I) is an imino substituent

And thus exist as syn or anti isomers or as a mixture of these isomers. All such isomeric forms are included within the scope of the present invention. In general, however, the syn isomer of the compound of formula (I) has the greatest activity.

Hereinafter, the present invention will be described in more detail with reference to the following examples.

Example 1

(±)-(Z) -2-[[[1- (2-amino-4-thiazolyl) -2-[[4,4, -dimethyl-2-oxo-1- (sulfooxy) -3- Azetidinyl] amino] -2-oxoethylidene] amino] oxy] -2-propenoic acid

A) 2-[(1,3-dioxo-2H-isoindol-2-yl) oxy] -2-propenic acid

A solution of 2-[(1,3-dioxo-2H-isoindol-2-yl) oxy-2-propenic acid and 1.75 g (5.7 mmol) of t-butyl ester was dissolved in 10 ml of methylene chloride and 10 ml of anisole. Treated with 5 ml of trifluoroacetic acid. After stirring overnight at room temperature, toluene was added thereto, and the reaction mixture was then concentrated in vacuo. The residue was treated twice with hexane to give 1.54 g of the title compound.

B) 2-[(1,3-dioxo-2H-isoindol-2-yl) oxy] -2-propenic acid, diphenylmethyl ester

1.54 g (4.8 mmol) of 2-[(1,3-dioxo-2H ㅗ -isoindol-2-yl) oxy] -2-propenoic acid are dissolved in 25 ml of acetonitrile, and diphenyldiazomethane is added thereto. A solution of 1.17 g (5.94 mmol) / 50 ml of acetonitrile was added dropwise. About 1.1 equivalents of diphenyldiazomethane were added thereto and measured by tlc showed that no starting material remained. A small amount of acetic acid was added to decompose excess diphenyldiomethane. The reaction solution was concentrated to give a residue, the residue was dissolved in ethyl acetate and then washed with 1N sodium bicarbonate and brine, dried over anhydrous magnesium sulfate and evaporated to give a solid. This solid was treated with hexane to give 1.9 g of the title compound.

C) 2-amino-α-[[[1- (diphenylmethoxy) carbonyl] -ethenyl] oxy] amino] -4-thiazole acetic acid

0.8 g (2 mmol) of 2-[(1,3-dioxo-2H-isoindol-2-yl) oxy] -2-propenoic acid and diphenylmethyl ester were dissolved in 50 ml of methylene chloride at 0 ° C. under argon. To the solution was added 100 mg of hydrazine hydrate (2 mmol in 1 ml of anhydrous ethanol). The reaction mixture was slowly warmed at 0 ° C. to room temperature for at least 1 hour and then further stirred at room temperature for 2 hours. The white precipitate was filtered off and the solution was diluted with diethyl ether and it was filtered again. The volatiles were removed from the filtrate to afford 2-aminooxy-2-propenic acid as a residue. 2-aminooxy-2-propene acid was dissolved in 6 ml of ethanol and 4 ml of water, and 0.31 g (1.8 mmol) of 2-aminothiazole-4-glyoxylic acid was added to this solution. The mixture was stirred at room temperature for 17 hours and then measured by tlc, indicating that the reaction was incomplete. To this was further added ethanol and water and a small amount of dimethylformamide was added to dissolve the reaction. The mixture was stirred for 72 hours and then measured by tlc, indicating that no 2-aminooxy-2-propenic acid remained. Evaporation gave the crude title compound, which was chromatographed on an HP20 column using an acetonitrile / water gradient (0-80%) as eluent. The fraction containing the product was concentrated to remove acetonitrile. The resulting aqueous slurry solution was filtered to give the title compound as a precipitate. After drying the precipitate door overnight in vacuo, 167 mg of the title compound was obtained.

D) N- (t-butyloxycarbonyl) -N ^2- (phenylmethoxy) -D, L-3-hydroxyvalineamide

A solution of 24.84 g (106.6 mmol) of Nt-butyloxycarbonyl-D, L-3-hydroxyvaline and 16.33 g (106.6 mmol) of hydroxybenzotriazole monohydrate was dissolved in 500 ml of dry tetrahydrofuran at -10 ° C. Cooled to, and 22 g (106.6 mmol) of dicyclohexylcarbodiimide was added thereto. The mixture was stirred for 1 hour under a nitrogen atmosphere of 0 ° C. A solution of 13.13 g (106.6 mmol) of O-benzylhydroxylamine dissolved in 250 ml of dry tetrahydrofuran was then added to the activated ester mixture for at least 15 minutes and the resulting mixture was added for 1 hour under a nitrogen atmosphere at 0 ° C. Stirred. The insoluble material was filtered off and the filtrate was evaporated in vacuo to give a foam. This foam was extracted using ethyl acetate and more insoluble material was removed by filtration. The filtrate was washed twice with 5% sodium bicarbonate solution. The organic phase was dried using sodium sulfate and evaporated to give a syrup, which was crystallized using 130 ml of isopropyl ether to give 24.7 g of the title compound. Melting Point: 76 °

-78 ℃

E) N- (t-butyloxycarbonyl) -N ^2- (phenylmethoxy) -D,

L-3- (sulfooxy) valineamide, pyridinium salt

8.08 ml (0.10 mol) of dry pyridine was placed in a 500 ml round bottom flask and cooled to −10 ° C. under a nitrogen atmosphere. 15.6 ml (0.10 mol) of trimethylsilyl chlorosulfonate was added dropwise with vigorous stirring using a magnetic stirrer, and then the reaction mixture, which was very concentrated due to precipitation of the product, was stirred at 0 ° C. for 0.5 hour. Chlorotrimethylsilane was removed in vacuo to give 15 g of pyridine-sulfur trioxide complex.

N- (t-butyloxycarbonyl) -N ^2- (phenylmethoxy) -D,

16.92 g (50 mmol) of L-3-hydroxyvalinamide were dissolved in 200 ml of dry pyridine, and 9.87 g (62.5 mmol) of pyridine-sulfur trioxide complex was added thereto. The mixture was stirred for 2 hours under a nitrogen atmosphere of 55 ° C. To this, 790 mg (5 mmol) of another portion of the pyridine-sulfur trioxide complex was added, and the stirring was continued for 1 hour or more. The reaction mixture was stripped in vacuo to give an oil. This oil was stripped three times with acetonitrile in vacuo to give a foamy crude title compound. Yield was quantitative.

F) (±) -3-[(t-butyloxycarbonyl) amino] -4,4-dimethyl-1- (phenylmethoxy) -2-azetidinone

A flask containing about 50 mmol of crude N- (t-butyloxycarbonyl) -N ^2- (phenylmethoxy) -D, L-3- (sulfooxy) -valinamide and pyridinium salt was placed in an ice bath, To this was added 400 ml of ethyl acetate and then a solution of 42.8 g (0.31 mol) of potassium carbonate dissolved in 90 ml of water with vigorous stirring. The resulting mixture was stirred vigorously for 2 hours under reflux under a nitrogen atmosphere. The reaction mixture was cooled to room temperature and each phase was separated. The aqueous phase was extracted using ethyl acetate (200 ml × 2 times), then all organic phases were combined, dried using sodium sulfate and evaporated in vacuo. The oil was dissolved in 125 ml of 40% ethyl acetate / hexanes and quickly filtered through 350 ml pads (10 cm) of Mallinkrodt SilicAR CC-7 using 40% ethyl acetate / hexanes 3-41. The filtrate was evaporated in vacuo to give 12.2 g of a solid. This was crystallized using 50 ml of isopropyl ether to give 7.15 g of the title compound (melting point: 110 ° C).

G) (±) -3- [t-butyloxycarbonyl) amino] -1-hydroxy-4,4-dimethyl-2-azetidinone

(±) -3- [Ct-butyloxycarbonyl) amino] -4,4-dimethyl-1

8.07 g (25 mmol) of 4-dimethyl-1- (phenylmethoxy) -2-azetidinone was hydrogenated at room temperature, atmospheric pressure for 2 hours using 0.6 g of 10% charcoal based palladium as catalyst in 40 ml of methanol. The reaction mixture was filtered through a pad of celite and the filtrate was concentrated to give 5.78 g of solid title compound.

H) (±) -3- [Ct-butyloxycarbonyl) amino] -4, 4-dimethyl-2-oxo-1-azetidinylsulfate, tetrabutylammonium salt

A solution of 12.27 g (0.105 mol) of chlorosulfonic acid dissolved in 210 ml of dichloromethane at -40 DEG C in an argon atmosphere was added dropwise to pyrodine 20.5 g (0.26 mol) for 10 minutes or more. The mixture was stirred at 0 ° C. for at least 10 minutes and then at 25 ° C. for 10 minutes. (±) -3- [Ct-butyloxycarbonyl) -amino] -1-hydroxy-4 in 20 ml of dichloromethane,

A slurry of 4-dimethyl-2-azetidinone was added and the mixture was stirred at 25 ° C. for 3.5 hours. This nearly uniform solution was then treated with 250 ml of water and 17 g (0.05 mol) of hydrogen tetrabutyl ammonium sulfate. This mixture was mixed well and the organic phase was separated and then dried using sodium sulfate. Evaporation in vacuo gave a foam, which was further purified by dissolving in ethyl acetate, removing insoluble matter and evaporating to give 30 g of the title compound on the foam.

I) (±) -3-amino-4, 4-dimethyl-2-oxo-azetidinyl sulfate (±) -3- [t-butyloxycarbonyl) amino] -4, 4-dimethyl-2- To a solution of oxo-1-1azetidinyl sulfate, 30 g (0.05 mol) of tetrabutylammonium salt, dissolved in -124 DEG C in 124 ml of dichloromethane and 10 ml of anisole under argon atmosphere, 50 ml of trifluoroacetic acid was added dropwise for 10 minutes Treatment. After stirring the mixture at -5 ° C to 0 ° C for 2.5 hours, the mixture was diluted with 50 ml of ethyl acetate and then filtered. The solid was washed with dichloromethane and then ethyl acetate and dried in vacuo to yield 9.4 g of the title compound as a white granular solid.

J) (±)-(Z) -2-[[[1- (2-amino-4-thiazolyl) -2-[[4,4-dimethyl-2-oxo-1- (sulfooxy) -3 -Azetidinyl] amino] -2-oxoethylidene] amino] oxy] -2-propenoic acid, diphenyl methyl ester

167 mg (0.4 mmol) 2-amino-α-[[[[[1- (diphenylmethoxy) carbonyl] ethenyl] oxy] amino] -4-thiazole-acetic acid at −30 ° C. under trigonal atmosphere To a solution of 56 μl (1.0 equiv) of ethyl amine, 1070 mg (0.4 mmol) of diphenyl chlorophosphate were added. The reaction mixture was stirred at -30 [deg.] C. for 1 hour to obtain mixed anhydride. (±) -3-amino-4,

126 mg (0.6 mmol) of 4-dimethyl-2-oxo-1-azetidinyl sulfate were dissolved in dimethylformamide at 0 ° C., and 71 μl (0.85 equiv) of this solution and triethylamine were mixed anhydride solution at −30 ° C. Added simultaneously. The reaction mixture was stirred at −30 ° C. for 0.5 h and then slowly warmed to 0 ° C. for 1 h. The reaction mixture was concentrated in vacuo, then dissolved in acetone / water and adjusted to pH 6.5 with 1N potassium bicarbonate. This was eluted using 30% acetone / water as eluent in the Dowex AG 50 (k ⁺ ) column. Appropriate fractions were combined and concentrated to place the residual aqueous solution on an HP20 column. The column was eluted with water and then eluted with acetone / water gradient eluent (0-100%). Appropriate fractions were combined and lyophilized to afford the title compound, which was all used in the next step.

K) (±)-(Z) -2-[[[1- (2-amino-4-thiazolyl) -2-[[4,4-dimethyl-2-oxo-1- (sulfooxy) -3 -Azetidinyl] amino] -2-oxoethylidene] amino] oxy] -2-propenoic acid

(±)-(Z) -2-[[[1- (2-amino-4-thiazolyl) -2-[[4,4-dimethyl-2-oxo-1- (sulfooxy) -3-ase 10 ml of methylene chloride and 10 ml of anisole were added to a flask containing thidinyl] amino] -2-oxoethylidene] amino] oxy] -2-propenoic acid and diphenylmethyl ester. After cooling the mixture to -5 ° C, 8 ml of trifluoroacetic acid was added thereto, and the reaction mixture was then stirred for 45 minutes under an argon atmosphere of -5 ° C to 0 ° C. Toluene was added thereto and the reaction mixture was evaporated to give a residue. Water and hexane were added to this residue, and each layer was separated. The aqueous layer was adjusted to pH 2.5 with 10% potassium bicarbonate. HP20 columns were used to elute first as water and then as acetone / water gradient eluent as eluent. Appropriate fractions were combined and lyophilized to afford the title compound as a white solid.

¹ H-NMR (1: 1 D ₂ O / CD ₃ CN); δ 1.57 (s, 3H); 1.75 (s, 3 H); 5.09 (s, 1 H); 5.75 (d, J = 2.3 Hz, 1H); 5.86 (d, J 2.3 Hz, 1 H); 7.42 (s, 1 H).

Example 2

[3S (Z)]-2-[[[1- (2-amino-4-thiazolyl-2-[[4, 4-dimethyl-2-oxo-1- (sulfooxy) -3-azetidinyl ] Amino] -2-oxoethylidene] amino] oxy] -2-propenic acid

A) 2-[(1,3-dioxo-2H-isoindol-2-yl) -oxy] -2-propenic acid

49.9 g (0.173 mol) of 2-[(1,3-dioxo-2H-isoindol-2-yl) -oxy] -2-propenoic acid and t-butyl ester were dissolved in 300 ml of methylene chloride and 150 ml of anisole. The solution was treated with 300 ml of trifluoroacetic acid. After the mixture was stirred overnight at room temperature, 800 ml of dry toluene was added thereto, and the reaction mixture was then concentrated in vacuo. The residue was treated twice with hexane to give 39.6 g of the title compound.

B) 2-[(1,3-dioxo-2H-isoindol-2-yl) oxy] -2-propenic acid, diphenylmethyl ester

39.6 g (0.17 mol) of 2-[(1,3-dioxo-2H-isoindol-2-yl) oxy] -2-propenoic acid are dissolved in 800 ml of acetonitrile, and a diphenyldiazomethane solution ( A solution of 43.4 g, 0.224 mol / acetonitrile) was added dropwise at 0 ° C. over 3 hours. The reaction solution was evaporated to give a solid, which was treated with hexane. The resulting solid was dissolved in dichloromethane and filtered through a silica gel pad (Kieselgel 60). Hexane was added to the filtrate to give 47.7 g of the title compound.

C) 2-aminoα-[[[1- (diphenylmethoxy) carbonyl] ethenyl] oxy] amino] -4-thiazole acetic acid

6.07 g (15.2 mmol) of 2-[(1,3-dioxo-2H-isoindol-2-yl) oxy] -2-propene acid and diphenylmethyl ester were dissolved in 375 ml of methylene chloride under argon atmosphere at 0 ° C. To the resulting solution, 0.76 g (15.2 mmol) of hydrazine hydrate in 4 ml of absolute ethanol was added. After 1 h at 0 [deg.] C., the mixture was evaporated at +10 [deg.] C. and dried and treated with ethyl ether. Got. This compound was then treated with a solution of 2.61 g (15.2 mmol) of 2-amino-4-thiazoleglyoxylic acid dissolved in 50 ml of dimethylformamide at 20 ° C. followed by 5 ml of water. The reaction was stirred at 20 ° C. for 20 hours, then cooled and diluted with 250 ml of water. The resulting gum was stirred to give a granular solid, which was filtered, washed with water and then azeotropically dried with acetonitrile to dry. This dry solid was slurried with 100 ml of acetonitrile and then filtered, and finally washed with acetonitrile, ethyl ether and hexane. Drying in air gave 1.97 g of the title compound.

D) N- (t-butyloxycarbonyl) -L-3-hydroxyvaline, α-methylbenzylamine salt

A solution of 7.02 g (30 mmol) of Nt-butyloxycarbonyl-D and L-3-hydroxyvaline in 250 ml of ethyl ether was dissolved in 3.63 g (30 mmol) of S-(-)-α-methyl benzylamine. Treated. After 8 hours, the resulting solids were filtered off. Recrystallization three times with acetonitrile gave 5.80 g of the title compound. Melting Point 146 ° -147 ℃

[α] _D = -4.5 ° (c = 2.0, methanol)

E) N- (t-butyloxycarbonyl) -L-3-hydroxyvaline

N- (t-butyloxycarbonyl) -L-3-hydroxyvaline,

A mixture of 204.6 g of α-methylbenzylamine salt (0.577 mol), ethyl acetate 3I, and 100 g of potassium bisulfate and 150 g of sodium chloride dissolved in water 1I was shaken, and after separating each layer, the organic phase was washed with water and sulfuric acid Dry with magnesium. The organic solution was concentrated and treated with 800 ml of hexane to give 136 g of the title compound. Melting Point: 120 °

-121 ℃

[α] _D = + 7.81 °

F) N- (t-butyloxycarbonyl) -N ^2- (phenylmethoxy) -L-3-hydroxyvalinamide

Reaction was carried out by D of Example 1, but instead of N- (t-butyloxycarbonyl) -D, L-3-hydroxyvaline, N- (t-butyloxycarbonyl) -L-3-hydride Roxyvaline was used to obtain the title compound.

G) (3S) -3-[(t-butyloxycarbonyl) amino] -4,4-dimethyl-1- (phenylmethoxy) -2-azetidinone

A solution of 296 ml (3.0 mol) of 2-methylpyridine dissolved in 2700 ml of methyl isobutyl ketone at -78 ° C under argon atmosphere was treated dropwise with 80 ml (1.2 mol) of chlorosulfonic acid for 30 minutes or more. After addition, the temperature of this mixture was brought to 25 ° C. for at least 30 minutes and held at this temperature for 30 minutes further. 338.4 g (1.0 mole) of N- (t-butyloxycarbonyl) -N ^2- (phenylmethoxy) -L-3-hydroxyvalinamide was added to this slurry, and the stirring was continued for 2 hours. To this mixture was added 800 ml of methyl isobutyl ketone, 1222 g (4.0 mol) of K ₂ B ₄ O ₇ 4H ₂ O, and 2700 ml of water, and the mixture was heated to 70 ° C. To this mixture was added dropwise at least 45 minutes with heating 1000 ml (2 mol) of 2N potassium hydroxide, and then the mixture was further heated for 55 minutes. Each layer was separated and the aqueous phase was extracted using 500 ml of methyl isobutyl ketone. The combined organic layers were cooled to 0 ° C. and washed with cooled 20% potassium bisulfate 3I and 1 l of ice water, followed by the addition of a solution of 50 g sodium bicarbonate and 100 g sodium chloride dissolved in 1 l of water. The organic layer was dried using sodium sulfate and concentrated in vacuo. The residue was crystallized using 1.75 l of isopropyl ether to give 161 g of the title compound. Melting Point: 121 °

-122 ℃

[α] _D = + 21.06 ° (c = 2.55, CH ₂ Cl ₂ ).

H) (3S) -3-[(t-butyloxycarbonyl) amino] -1-hydroxy-4,

4-dimethyl-2-azetidinone

(3S) -3-[(t-butyloxycarbonyl) amino] -4,4-dimethyl-1- (phenylmethoxy) -2-azetidinone 14.77 g (0.0461 mol) was added 15 ml of ethanol and 85 ml of ethyl acetate. The solution dissolved in the water was hydrogenated using 0.75 g of a 5% carbon based palladium catalyst for 1.5 hours at 1 atmosphere. The reaction mixture was filtered and concentrated to give a white solid. This solid was recrystallized using ethyl acetate to give 8.82 g of the title compound.

Melting Point: 148 °

-149 ℃

[a] _D = + 31 ° (c = 1, ethyl acetate)

I) (3S) -3-[(t-butyloxycarbonyl) amino] -4,4-dimethyl-2-oxo-1-azetidinyl sulfate, tetrabutyl ammonium salt

The reaction was carried out according to the method of Example 1, except that (±) -3-[(t-butyloxycarbonyl) amino] -1-hydroxy-4,

Instead of 4-dimethyl-2-azetidinone, using (3S) -3-[(t-butyloxycarbonyl) amino] -1-hydroxy-4,4-dimethyl-2-azetidinone, The title compound on the foam was obtained.

J) (3S) -3-amino-4,4-dimethyl-2-oxo-1-azetidinyl sulfate

The reaction is carried out by the method I of Example 1, wherein (±) -3-[(t-butyloxycarbonyl) amino] -4,4-dimethyl-2-oxo-1-azetidinyl sulfate, tetrabutyl Instead of ammonium salts, the title compound was obtained using (3S) -3-[(t-butyloxycarbonyl) amino] -4,4-dimethyl-2-oxo-1-azetidinyl sulfate, tetrabutylammonium salt. . A small amount of sample was recrystallized using ethanol / water to afford the title compound as a crystalline solid.

Melting Point: 140 °

-142 ° C (decomposition)

[α] _D = 74.8 ° (c = 1, H ₂ O)

K) [3S (Z)]-2-[[[1- (2-Amino-4-thiazolyl) -2-[[4,4-dimethyl-2-oxo-1- (sulfooxy) -3- Azetidinyl] amino] -2-oxoethylidene] amino] oxy] -2-propenoic acid, diphenylmethyl ester, tetrabutylammonium salt at -30 ° C., 2-amino-α-[[[[ 0.902 g of diphenyl chlorophosphate in a solution of 1.423 g (3.36 mmol) of 1- (diphenylmethoxy) carbonyl] ethenyl] oxy] amino] -4-thiazole acetic acid and 0.404 g (3.88 mmol) of triethylamine 3.36 mmol) was added. The reaction mixture was stirred at -30 ° C for 1 hour to give mixed anhydride. 0.706 g (3.36 mmol) of (3S) -3-amino-4,4-dimethyl-2-oxo-1-azetidinyl sulfate was dissolved in 4 ml of dimethylformamide at 0 ° C., this solution and triethylamine 0.404 g (3.88 mmol) was added simultaneously to the mixed anhydride solution at -30 ° C. The reaction mixture was slowly warmed to 0 ° C. for 1 h. The reaction mixture was treated with 0.338 g (3.36 mmol) triethylamine and then concentrated in vacuo. The residue was treated with water to give a gum, which was separated from the aqueous layer and washed again with water. The gum was dissolved in 100 ml of methylene chloride, and the solution was shaken by adding a solution of 1.14 g (3.36 mmol) of hydrogen tetrabutylammonium sulfate dissolved in 30 ml of water. The organic phase was separated, washed three times with water, dried with sodium sulfate and evaporated to give a foam. The foam was dissolved in 30 ml of methylene chloride and diluted to 120 ml by addition of ethyl acetate. This was crystallized to give 1.73 g of the title compound as a white solid. Melting Point: 170 °

-172 ℃

L) [3S (Z)]-2-[[[1- (2-Amino-4-thiazolyl) -2-[[4,4-dimethyl-2-oxo-1- (sulfooxy) -3- Azetidinyl] amino] -2-oxoethylidene] amino] oxy] -2-propenoic acid

[3S (Z)]-2-[[[1- (2-amino-4-thiazolyl) -2-[[4,4-dimethyl-2-oxo-1- (sulfooxy) -3-azeti Diyl] amino] -2-oxoethylidene] amino] oxy] -2-propenic acid, diphenylmethyl ester, 2.17 g (2.54 mmol) of tetrabutylammonium salt were dissolved in 24 ml of methylene chloride and 1 ml of anisole at -12 ° C. The resulting solution was treated with 8 ml of trifluoro acetic acid and the reaction mixture was stirred at -10 ° C. under argon atmosphere for 1 hour. The mixture was treated dropwise with 60 ml of ethyl acetate and the resulting slurry was stirred for 20 minutes, then filtered and washed with ethyl acetate and hexanes. After drying in air, the solid was slurried at 50C with 50 ml of water to form crystals within minutes. After crystallization, the solution was filtered, the solid was washed with water and dried in vacuo to give 0.9 g of the title compound. Melting Point: 140 °

-170 ° C (decomposition).

Example 3

(±)-(Z)-[[[1- (2-amino-4-thiazolyl) -2-oxo-2-[[2-oxo-1- (sulfooxy) -1-azaspiro [3.3] Hept-3-yl] amino] ethylidene] amino] oxy] -2-propenic acid

A) N- (t-butoxycarbonyl) -α- (1-hydroxycyclobutyl) -glycine, benzyl ester

A solution of 9.7 ml (70 mmol) of diisopropylamine dissolved in 150 ml of dry tetrahydrofuran at -40 ° C. under argon atmosphere was treated with 39 ml (64.5 mmol) of 1.71N n-butyllidium in hexane, which was pale yellow. The solution was stirred at -40 ° C for 20 minutes. The solution was cooled to -78 deg. C, and a solution obtained by dissolving N- (t-butoxycarbonyl) glycine and 7.95 g (30 mmol) of benzyl ester in 30 ml of dry tetrahydrofuran was added dropwise for 5 minutes. A yellow solution was obtained, which had some turbidity after 20 minutes. After 0.5 hour, a solution in which 2.42 g (2.0 ml, 34.5 mmol) of cyclobutanone was dissolved in 30 ml of tetrahydrofuran was added thereto. The resulting yellow turbid mixture was stirred at −78 ° C. for 15 minutes and then left in an ice bath at 0 ° C. for 2 hours. After 1 hour at internal temperature -25 [deg.] C. the solution became clear and at -15 [deg.] C. dark purple. This was stirred at 0 ° C. for 0.5 hour and then treated with 3.96 g (66 mmol) of glacial acetic acid in 15 ml of tetrahydrofuran to give a pale yellow cloudy mixture. It was poured into 500 ml of cold water and extracted twice with ethyl acetate. The extract was washed with 2% potassium bisulfate, 5% sodium bicarbonate and brine, dried using sodium sulfate and evaporated to give a dark oil. This oil was chromatographed using hexane / ethyl acetate (2: 1) as eluent, 800 ml of LPS-1, and the product fraction (Rf = 0.29) was combined to give 7.8 g of oily product.

B) N- (t-butoxycarbonyl) -α- (1-hydroxycyclobutyl) -glycine

N- (t-butoxycarbonyl) -α- (1-hydroxycyclobutyl) -glycine and 7.8 g (23.3 mmol) of benzyl esters were prepared using 1.0 g of 10% charcoal based palladium catalyst in 150 ml of anhydrous ethanol. Hydrogenation was carried out for 4 hours at 1 ° C. The catalyst was filtered off and the solvent was evaporated in vacuo. Benzene was added thereto and evaporated twice to obtain 5.0 g of a hard foamy product.

C) N- (benzyloxy) -N ^2- (t-butoxycarbonyl) -α- (1-hydroxycyclobutyl) -lysineamide

5.0 g (20.4 mmol) of N- (t-butoxycarbonyl) -α- (1-hydroxycyclobutyl) -glycine were dissolved in 150 ml of dry tetrahydrofuran under argon atmosphere. To this was added 3.12 g (20.4 mmol) of hydroxybenzotriazole hydrate and the mixture was cooled to 0 ° C. and then treated with 4.20 g (20.4 mmol) of dicyclohexyl carbodiimir. After 1.75 hours at 0 ° C., an O-benzylhydroxylamine solution dissolved in 15 ml of tetrahydrofuran was added thereto and the mixture was stirred at 0 °.

Stir at -25 ° C for 17 h. The tetrahydrofuran mixture was cooled to −10 ° C. for 20 minutes and the resulting solids were filtered off and then washed using dry tetrahydrofuran. The filtrate was evaporated and the residue was dissolved in ethyl acetate, washed rapidly with 2% potassium bisulfate, brine, 5% sodium bicarbonate and brine, then dried over sodium sulfate and evaporated to give a foam. This was treated with isopropyl ether to obtain 4.69 g of a white solid product. Melting Point: 95 °

-97 ℃

D) 1- (benzyloxy) -3-[(t-butoxycarbonyl) amino] -2-oxo-1-azaspiro [3.3] heptane

3.50 g (10 mmol) of N- (benzyloxy) -N ^2- (t-butoxycarbonyl) -α- (1-hydroxycyclobutyl) glycinamide in 200 ml of dry tetrahydrofuran under an argon atmosphere at 0 ° C Treatment with diethylazodicarboxylate 2.4 ml (15 mmol) followed by a solution of 5.2 g (20 mmol) triphenylphosphine in 50 ml tetrahydrofuran for at least 10 minutes and the mixture at 0 ° C. Stir for 1 hour. 0.52 g (2 mmol) of triphenylphosphine was added because yellow persisted. After 15 minutes, it was evaporated in vacuo to give an oil. The oil was treated with 100 ml of hexane / ethyl acetate (2: 1) to give a white solid which was filtered off. The filtrate was chromatographed with 800 ml of LPS-1 to give the product fraction [Rf = 0.8 in eluent hexane / ethyl acetate (1: 1)] which was contaminated with impurities eluted at similar rates. The product was removed using isopropyl ether to obtain 1.07 g of a product as a white solid.

-157 ℃

E) 3-[(t-butoxycarbonyl) amino] -2-oxo-1- (sulfooxy) -1-azaspiro [3.3] heptane, monosodium salt

1.07 g (3.22 mmol) of 1- (benzyloxy) -3-[(t-butoxycarbonyl) amino] -2-oxo-1- (sulfooxy) -1-azaspiro [3.3] heptane under 1 atm In 30 ml of absolute ethanol, 0.4 g of 10% charcoal based palladium catalyst was hydrogenated at 25 DEG C for 3 hours. The catalyst was filtered off, and the solvent was removed in vacuo at 10 ° C. to obtain a solid. This was dissolved in 19 ml of dry pyridine and treated with 1.44 g (9 mmol) of pyridine-sulfur trioxide under an argon atmosphere at 25 ° C. After 4 hours, the volatiles were removed in vacuo, the residue was dissolved in water and the pH (5.40) was adjusted to 6.45 using dilute sodium bicarbonate. Water was used as the eluent to elute the product within 300 ml by passing through a 40 ml Dowex AG50 (K ⁺ ) column. It was lyophilized to give a white solid which was eluted with HP-20 column, first with water and then chromatographed with acetone (20%) with increasing gradient. The resulting fractions were lyophilized to yield 0.75 g of a white powder product.

F) 3-amino-2-oxo-1- (sulfooxy) -1-azaspiro [3.3] heptane

0.3 g (0.87 mmol) of 3-[(t-butoxycarbonyl) amino] -2-oxo-1- (sulfooxy) -1-azaspiro [3.3] heptane, monosodium salt at -10 ° C., argon Under atmosphere, slurried in 2.5 ml of dry dichloromethane and 1.0 ml of anisole and then treated with 4.0 ml of trifluoroacetic acid. After 0.5 hour, a solid formed. After 1.5 hours, 4 ml of dry toluene was added thereto and the mixture was evaporated in vacuo to give 3-amino-2-oxo-1- (sulfooxy) -1-azaspiro [3.3] heptane as a solid, which was Treated twice with hexane and dried at 25 ° C. in vacuo for 1 hour.

G) (±)-(Z)-[[[1- (2-amino-4-thiazolyl) -2-oxo-2-[[2-oxo-1- (sulfooxy) -1-azaspiro [ 3.3] hept-3-yl] amino] ethylidene] amino] oxy] -2-propenoic acid, diphenylmethyl ester, tetrabutyl ammonium salt

The reaction was carried out by the method K of Example 2, except that instead of (3S) -3-amino 4,4-dimethyl-2-oxo-1-azetidinyl sulfate, 3-amino-2-oxo-1- ( Sulfooxy) -1-azaspiro [3.3] heptane was used to obtain the title compound.

H) (±)-(Z)-[[[1- (2-amino-4-thiazolyl) -2-oxo-2-[[2-oxo-1- (sulfooxy) -1-azaspiro [ 3.3] hept-3-yl] amino] ethylidene] amino] oxy-2-propenoic acid

The reaction was carried out by the method L of Example 2, wherein [3S (Z)]-2-[[[1- (2-amino-4-thiazolyl) -2-[[4,4-dimethyl-2-oxo -1- (sulfooxy) -3-azetidinyl] amino] -2-oxoethylidene] amino] oxy] -2-propenoic acid,

Diphenylmethyl ester,

Instead of tetrabutylammonium salt, (±)-(Z)-[[[1- (2-amino-4-thiazolyl) -2-oxo-2-[[2-oxo-1- (sulfooxy) -1 -Azaspiro [3.3] hept-3-yl] amino] ethylidene] amino

The precipitate precipitated from the diluent of ethyl acetate using oxy] -2-propenic acid, diphenylmethyl ester and tetrabutylammonium salt was chromatographed using HP-20 resin without recrystallization with water, and the title compound. Got.

Melting Point: 170 °

-200 ° C (decomposition)

Claims (2)

Compound represented by the following structural formula

In the above formula, A ₁ is a carboxyl protecting group, A ₂ is hydrogen or an amino protecting group, and R ₃ and R ₄ are the same or different from each other, and are each hydrogen or an alkyl group having 1 to 3 carbon atoms. Structural formula

Of a compound represented by the following structural formula

A structural formula characterized by reacting a compound of

[Wherein A ₁ is a carboxyl protecting group, A ₂ is an amino protecting group, and R ₃ and R ₄ are the same or different from each other and are each hydrogen or an alkyl group having 1 to 3 carbon atoms.] Manufacturing method.