KR20020016381A - Novel 1β-Methylcarbapenem derivatives having 5'-heteroarylthiomethylpyrrolidin-3'-ylthio group and process for preparation thereof - Google Patents

Abstract

PURPOSE: Provided are a novel 1-β-methylcarbapenem derivative useful as antibiotics, its pharmaceutically acceptable salt, its manufacturing method and a pharmaceutical composition. containing it. CONSTITUTION: 1-β-methylcarbapenem derivative is represented by the formula(1), wherein R is represented by formulae; X is trifluormethyl or C1-C3 alkyl; Y is C1-C3 linear or branched aliphatic alkyl, C1-C3 sulfonamido alkyl in which one or two C1-C3 alkyl groups are substituted, C1-C3 alkyl substituted or unsubstituted C1-C3 carbo amidoalkyl group, C1-C3 hydroxyalkyl group, and C1-C3 alkyl substituted C1-C3 aminoalkyl or aryl; and Z is C1-C3 alkyl group.

Description

Novel 1β-Methylcarbapenem derivatives having 5'-heteroarylthiomethylpyrrolidin-3'-ylthio group and process for 5'-heteroarylthiomethylpyrrolidin-3'-ylthio group preparation

The present invention relates to novel 1-betamethylcarbapenem derivatives, pharmaceutically acceptable salts thereof, methods for their preparation and pharmaceutical compositions comprising the same, more particularly 1-betamethylcarba By containing 5'-heteroarylthiomethylpyrrolidin-3'-ylthio group as the main functional group at the 2nd position of the penem nucleus, it shows excellent antibacterial activity against both Gram-positive bacteria and Gram-negative bacteria, It relates to a stable 1-betamethyl carbapenem derivative, a preparation method thereof and a pharmaceutical composition for an antimicrobial agent using the compound as an active ingredient.

Formula 1

In the above formula,

R is ego,

X is trifluoromethyl or an alkyl group of C _{1 to} C ₃ ,

Y is substituted with an alkyl group of C ₁ ~C ₃ straight or branched chain aliphatic alkyl group a, C ₁ ~C ₃ alkyl group is substituted with one or two C ₁ ~C ₃ of sulfone amido group, C ₁ ~C ₃ of the or an unsubstituted C ₁ ~C ₃ alkyl group of the carboxylic bore not shown, C ₁ ~C ₃ alkyl group of hydroxy, C ₁ ~C a C ₁ ~C ₃ alkyl group substituted with _{3-amino-alkyl} group or an aryl group,

Z represents an alkyl group of C ₁ ~C _3.

Carbapenem-based antimicrobial agent exhibits a broader antimicrobial activity than conventional cephalosporin-based or penicillin-based antimicrobial agents, as well as excellent effects against resistant bacteria. However, these carbapenem type antimicrobial agents are easily decomposed and inactivated by the enzyme dehydropeptidase-I (abbreviated as "DHP-I"), which is present in the kidney, and thus loses antimicrobial activity. Reported. ( J. Antibiot ., 1991 , 1172-1177, Antimicrobial Agent and Chemotherapy, 1992 , 1577-1579)

Accordingly, many studies have been conducted to solve the above problems, and as a result, compounds having 1-betamethyl groups introduced into the carbapenem nucleus exhibit a broad antimicrobial spectrum against Gram-positive and Gram-negative bacteria, as well as high stability against DHP-I. Figured out. Meropenem has recently been commercialized as a derivative of this, and BO-2727, S-4661, ZD-4433, ER-35786, FR-21818 and IH201 are in clinical or animal testing. ( J. Antibiot ., 1990 , 43 , 519; Yamaji, E. et al . Abstracts of Papers, H141, 35th Interscience Conference on Antimicrobial Agents and Chemotheraphy, San Francisco, CA, 17-20 Sep. 1995; Arakawa, S. et al . Abstracts of Papers, F218, 37th Interscience Conference on Antimicrobial Agents and Chemotheraphy, Toronto, Ontario, 28 Sep.-1 Oct. 1997; Pelak, BA et al . Abstracts of Papers, F119, 36th Interscience Conference on Antimicrobial Agents and Chemotheraphy, New Orleans, LA, 15-18 Sep. 1996; Sato, N. et al . Abstracts of Papers, F151, 35th Interscience Conference on Antimicrobial Agents and Chemotheraphy, San Francisco, CA, 17-20 Sep. 1995; Tawara, S. et al . Abstracts of Papers, F145, 35th Interscience Conference on Antimicrobial Agents and Chemotheraphy, San Francisco, CA, 17-20 Sep. 1995; Shin, KJ et al . Bioorg.Med. Chem. Lett. 1998 , 8 , 1607 .)

Accordingly, the present inventors have repeatedly studied to develop a new carbapenem compound showing high stability against DHP-I and showing excellent antimicrobial activity against both Gram-positive bacteria and Gram-negative bacteria, and as a main functional group at the position 2 of the carbapenem nucleus. Novel 1-betamethylcarbapenem derivatives substituted with 5'-heteroarylthiomethylpyrrolidin-3'-ylthio group were synthesized, and these compounds showed high stability against DHP-I and were not only Gram-positive bacteria but also Gram-negative bacteria. The antimicrobial effect was found to complete the present invention.

It is an object of the present invention to provide 1-betamethylcarbapenem derivatives represented by the formula (1) and pharmaceutically acceptable salts thereof.

Another object of the present invention is to provide a method for preparing new 1-betamethylcarbapenem derivatives and pharmaceutically acceptable salts thereof.

It is also an object of the present invention to provide a method for preparing a thiol derivative which is an intermediate of a novel 1-betamethylcarbapenem derivative.

It is also an object of the present invention to provide a pharmaceutical composition for antimicrobial agents having a 1-betamethyl carbapenem derivative represented by Formula 1 as an active ingredient and stable against DHP-I and showing strong antimicrobial activity against gram positive and gram negative bacteria. will be.

In order to achieve the above object, in the present invention, 1-betamethylcarba in which 5'-heteroarylthiomethylpyrrolidin-3'-ylthio group is substituted as a main functional group at position 2 of 1-betamethylcarbapenem nucleus Penem derivatives and pharmaceutically acceptable salts thereof.

Formula 1

In the above formula,

R is ego,

X is trifluoromethyl or an alkyl group of C _{1 to} C ₃ ,

Y is substituted with an alkyl group of C ₁ ~C ₃ straight or branched chain aliphatic alkyl group a, C ₁ ~C ₃ alkyl group is substituted with one or two C ₁ ~C ₃ of sulfone amido group, C ₁ ~C ₃ of the or an unsubstituted C ₁ ~C ₃ alkyl group of the carboxylic bore not shown, C ₁ ~C ₃ alkyl group of hydroxy, C ₁ ~C a C ₁ ~C ₃ alkyl group substituted with _{3-amino-alkyl} group or an aryl group,

Z represents an alkyl group of C ₁ ~C _3.

To the tetrazole of the one or two alkyl groups of the C ₁ ~C ₃ substituted in position 1 C ₁ ~C ₃ sulfone amido group is preferably a methyl sulfone amido group or dimethyl sulfone amido group.

Also shown carboxylic bore alkyl C ₁ ~C ₃ alkyl group or an unsubstituted C ₁ ~C ₃ is substituted by a group shown is preferably a carboxylic bore, the bore not shown methylcarbamoyl group or a methylcarbamoyl group bore shown.

Moreover, it is preferable that an aryl group is a phenyl group or a pyridine group.

More preferably, 1-betamethylcarbapenem derivative represented by Formula 1 is

1) (1 R , 5 S , 6 S , 8 R , 3 ' S , 5' S ) -2- [5 '-(1-thia-2,3-diazol-5-ylthio) methyl-pi Ralidin-3'-ylthio] -6- (1-hydroxyethyl) -1-methylcarbafen-2-m-3-carboxylic acid,

2) (1 R , 5 S , 6 S , 8 R , 3 ' S , 5' S ) -2- [5 '-(1- (2-dimethylaminoethyl) -1,2,3,4-tetra Sol-5-ylthio) methyl-pyrrolidine-3'-ylthio] -6- (1-hydroxyethyl) -1-methylcarbafen-2-m-3-carboxylic acid,

3) (1 R , 5 S , 6 S , 8 R , 3 ' S , 5' S ) -2- [5 '-(1- (2-trimethylammoniumethyl) -1,2,3,4- Tetrazol-5-ylthio) methyl-pyrrolidine-3'-ylthio] -6- (1-hydroxyethyl) -1-methylcarbafen-2-m-3-carboxylic acid salt,

4) (1 R , 5 S , 6 S , 8 R , 3 ' S , 5' S ) -2- [5 '-(1-methyl-1,2,3,4-tetrazol-5-ylthio ) Methyl-pyrrolidine-3'-ylthio] -6- (1-hydroxyethyl) -1-methylcarbafen-2-m-3-carboxylic acid,

5) (1 R , 5 S , 6 S , 8 R , 3 ' S , 5' S ) -2- [5 '-(1- (2-hydroxyethyl) -1,2,3,4-tetra Sol-5-ylthio) methyl-pyrrolidine-3'-ylthio] -6- (1-hydroxyethyl) -1-methylcarbafen-2-m-3-carboxylic acid,

6) (1 R , 5 S , 6 S , 8 R , 3 ' S , 5' S ) -2- [5 '-(1-phenyl-1,2,3,4-tetrazol-5-ylthio ) Methyl-pyrrolidine-3'-ylthio] -6- (1-hydroxyethyl) -1-methylcarbafen-2-m-3-carboxylic acid,

7) (1 R , 5 S , 6 S , 8 R , 3 ' S , 5' S ) -2- [5 '-(1- (pyridin-4-yl) -1,2,3,4-tetra Sol-5-ylthio) methyl-pyrrolidine-3'-ylthio] -6- (1-hydroxyethyl) -1-methylcarbafen-2-m-3-carboxylic acid,

8) (1 R , 5 S , 6 S , 8 R , 3 ' S , 5' S ) -2- [5 '-(1- (2-dimethylsulfonamidoethyl) -1,2,3,4 -Tetrazol-5-ylthio) methyl-pyrrolidine-3'-ylthio] -6- (1-hydroxyethyl) -1-methylcarbafen-2-m-3-carboxylic acid,

9) (1 R , 5 S , 6 S , 8 R , 3 ' S , 5' S ) -2- [5 '-(1- (2-methylsulfonamidoethyl) -1,2,3,4 -Tetrazol-5-ylthio) methyl-pyrrolidine-3'-ylthio] -6- (1-hydroxyethyl) -1-methylcarbafen-2-m-3-carboxylic acid,

10) (1 R , 5 S , 6 S , 8 R , 3 ' S , 5' S ) -2- [5 '-(1- (2-carboamidoethyl) -1,2,3,4- Tetrazol-5-ylthio) methyl-pyrrolidine-3'-ylthio] -6- (1-hydroxyethyl) -1-methylcarbafen-2-m-3-carboxylic acid,

11) (1 R , 5 S , 6 S , 8 R , 3 ' S , 5' S ) -2- [5 '-(1- (2-methylcarboamidoethyl) -1,2,3,4 -Tetrazol-5-ylthio) methyl-pyrrolidine-3'-ylthio] -6- (1-hydroxyethyl) -1-methylcarbafen-2-m-3-carboxylic acid,

12) (1 R , 5 S , 6 S , 8 R , 3 ' S , 5' S ) -2- [5 '-(1- (methylcarboamidomethyl) -1,2,3,4-tetra Sol-5-ylthio) methyl-pyrrolidine-3'-ylthio] -6- (1-hydroxyethyl) -1-methylcarbafen-2-m-3-carboxylic acid,

13) (1 R , 5 S , 6 S , 8 R , 3 ' S , 5' S ) -2- [5 '-(1- (dimethylcarboamidomethyl) -1,2,3,4-tetra Sol-5-ylthio) methyl-pyrrolidine-3'-ylthio] -6- (1-hydroxyethyl) -1-methylcarbafen-2-m-3-carboxylic acid,

14) (1 R , 5 S , 6 S , 8 R , 3 ' S , 5' S ) -2- [5 '-(4-methylpyrimidin-2-ylthio) methyl-pyrrolidine-3' -Ylthio] -6- (1-hydroxyethyl) -1-methylcarbafen-2-m-3-carboxylic acid,

15) (1 R , 5 S , 6 S , 8 R , 3 ' S , 5' S ) -2- [5 '-(4-trifluoromethylpyrimidin-2-ylthio) methyl-pyrrolidine -3'-ylthio] -6- (1-hydroxyethyl) -1-methylcarbafen-2-m-3-carboxylic acid,

16) (1 R , 5 S , 6 S , 8 R , 3 ' S , 5' S ) -2- [5 '-(1-methyl-1,3,4-triazol-5-ylthio) methyl -Pyrrolidine-3'-ylthio] -6- (1-hydroxyethyl) -1-methylcarbafen-2-m-3-carboxylic acid, or

17) (1 R , 5 S , 6 S , 8 R , 3 ' S , 5' S ) -2- [5 '-(2-methyl-1-thia-3,4-diazol-5-ylthio ) Methyl-pyrrolidine-3'-ylthio] -6- (1-hydroxyethyl) -1-methylcarbafen-2-m-3-carboxylic acid.

1-betamethylcarbapenem derivatives of the present invention represented by Formula 1 may be used in the form of a pharmaceutically acceptable salt, and acid salts formed by pharmaceutically acceptable free acid are useful as salts. Do. Inorganic acids and organic acids can be used as the free acid. Hydrochloric acid, bromic acid, sulfuric acid, phosphoric acid, etc. may be used as the inorganic acid, and citric acid, acetic acid, lactic acid, tartaric acid, maleic acid, fumaric acid, gluconic acid, methanesulfonic acid, glyconic acid, succinic acid, 4-toluenesulfonic acid , Gluturonic acid, embonic acid, glutamic acid, aspartic acid, or the like can be used. The compound of formula 1 may also be a pharmaceutically acceptable metal salt, in particular an alkali metal salt, formed due to the base. Examples of these are sodium salts and potassium salts.

The present invention also provides a method for producing a novel 1-betamethylcarbapenem derivative represented by the formula (1).

Scheme 1 shows a method for preparing a compound of the present invention.

(In Scheme 1, R is as defined in Formula 1, R 'is a carboxyl protecting group.)

Method for preparing a 1-betamethyl carbapenem derivative represented by the formula (1)

1) reacting carbapenem intermediate (III) with thiol derivative (II) in the presence of a base in a suitable solvent to prepare a protected carbapenem derivative (IV) (step 1), and

2) deprotecting the protected carbapenem derivative (IV) obtained in step 1 to prepare 1-betamethylcarbapenem derivative (I) (step 2).

The carbapenem intermediate of Structural Formula (III) used as starting material in step 1 was prepared by a known method (Catchpole, CR et al . Antimicrob. Agents Chemother. 1992 , 36 , 1928).

In more detail, the step 1 may be used as a base, a tertiary organic amine having a low basicity. For example, trimethylamine, triethylamine, diisopropylethylamine, 2,6-lutidine, Preference is given to using organic bases such as picoline, N, N -dimethylaniline, pyridine, 4-dimethylaminopyridine and the like. The reaction is reacted at a reaction temperature of 0 ° C. for 3 to 6 hours to obtain a protected carbapenem derivative of formula (IV). At this time, it is preferable to use acetonitrile as the reaction solvent.

The deprotection reaction of the protected carbapenem derivative represented by the formula (IV) in step 2 may use methods well known in the art of carbapenem. The protecting group R 'is preferably an allyl, paramethoxybenzyl or paranitrobenzyl group as the carboxy protecting group.

When the protecting group R 'is an allyl group, it can be removed by using a palladium zero-valent catalyst such as tetrakistriphenylphosphine palladium and n- Bu ₃ SnH, where carbon dichloride is preferably used as the reaction solvent. After 1 hour of reaction at 1-betamethylcarbapenem derivative of the present invention can be obtained. If the protecting group is paramethoxybenzyl, it is removed by reaction in the presence of aluminum trichloride (AlCl ₃ ) in anisole. If the protecting group is a paranitrobenzyl group, it can be removed by a reduction method. Specifically, palladium carbon is used as a catalyst for 3 hours at a reaction temperature of 20 to 30 ° C. in a mixed solution of water and tetrahydrofuran (1: 1). While protecting under 2 atmospheres of hydrogen to remove the protecting group, or in a pH 6.2 phosphate buffer solution, the protecting group can be removed by reacting with zinc at 20 to 30 ° C. for 3 to 5 hours.

The present invention provides a thiol derivative represented by the formula (2) as an intermediate.

In the above formula,

R is ego,

X is trifluoromethyl or an alkyl group of C _{1 to} C ₃ ,

Y is substituted with an alkyl group of C ₁ ~C ₃ straight or branched chain aliphatic alkyl group a, C ₁ ~C ₃ alkyl group is substituted with one or two C ₁ ~C ₃ of sulfone amido group, C ₁ ~C ₃ of the or an unsubstituted C ₁ ~C ₃ alkyl group of the carboxylic bore not shown, C ₁ ~C ₃ alkyl group of hydroxy, C ₁ ~C a C ₁ ~C ₃ alkyl group substituted with _{3-amino-alkyl} group or an aryl group,

Z represents an alkyl group of C ₁ to C ₃ ,

R 'is a carboxy protecting group.

In the present invention, the thiol compound represented by Formula 2 may be obtained through a series of reaction processes as shown in Scheme 2 as an example.

The thiol-based compound of formula (II) used to prepare the 1-betamethylcarbapenem derivative of the present invention

1) condensation reaction of an iodine compound of formula (V) with a mercapto heteroaromatic compound of formula (VI) in a suitable solvent to prepare a thio acetyl compound (VII), and

2) It is obtained from the step (step 3) of obtaining a thiol compound (II) by hydrolyzing the thioacetyl compound (iii) obtained in step 1 above.

The iodine compound (V) used as starting material in step 1 is prepared by a method similar to the known method (Ohtake, N. et al. J. Antibiotics 1997 , 50 , 567), and the thiol compound of formula (VI) It can be purchased or prepared using methods analogous to existing synthetic methods (Berges, DA et al. J. Heterocyclic Chem. 1978 , 15 , 981).

Specifically, it is preferable to use potassium carbonate, sodium carbonate, etc. as the base in step 1, and the reaction solvent may use acetone, acetonitrile or dimethylformamide, and acetone is most preferable. It is preferable to make reaction react at 50-90 degreeC for 3 to 5 hours.

In step 2, the thioacetyl-based compound of formula (VII) is preferably obtained by hydrolysis using an aqueous sodium hydroxide solution in a mixed solution of methanol and carbon dichloride. Preferably, the reaction is carried out at 0 ° C. for 30 minutes to obtain a thiol compound of Chemical Formula 2.

In another aspect, the present invention provides a pharmaceutical composition for antimicrobial agents containing the compound of formula (1) as an active ingredient.

The novel 1-betamethylcarbapenem derivatives of the present invention have significant antimicrobial activity as compared to conventional imipenem or meropenem antimicrobial agents as a result of measuring Minimum Inhibitory Concentration (MIC, μg / ml). The results of the activity were obtained, and the compounds of the present invention showed excellent antimicrobial effects against both Gram-positive bacteria and Gram-negative bacteria, and are stable against DHP-I, and thus have high bioavailability.

The present invention provides, in addition to non-toxic, inert, pharmaceutically suitable excipients, pharmaceutical compositions consisting of one or more compounds according to the invention and methods of preparing said compositions.

The compound of formula 1 may be administered parenterally during clinical administration and may be used in the form of a general pharmaceutical formulation.

That is, the compound of formula 1 of the present invention may be administered in various parenteral formulations during actual clinical administration, and preparations for parenteral administration include sterile aqueous solutions, non-aqueous solvents, suspensions, emulsions, and lyophilized agents. . As the non-aqueous solvent and the suspension solvent, propylene glycol, polyethylene glycol, vegetable oil such as olive oil, injectable ester such as ethyl oleate and the like can be used.

To formulate into a parenteral formulation, the compound of Formula 1 is mixed in water with a stabilizer or buffer to prepare a solution or suspension, which is formulated in unit dosage forms of ampoules or vials.

In general, in medicine, the effective dose of the compound of formula 1 according to the present invention is 0.1 to 100 mg / kg, preferably 0.1 to 10 mg / kg, and may be administered once to several times a day. However, the dosage may need to be changed, and in particular, may be changed in consideration of the constitution specificity and weight of the subject to be treated, the type and depth of the disease, the nature of the formulation, the nature of the drug administration, and the duration or interval of administration.

Hereinafter, the present invention will be described in detail by preparation examples and examples. However, the following examples are merely to illustrate the invention and the present invention is not limited by the examples.

<Example 1> (One R , 5 S , 6 S , 8 R , 3 ' S , 5 ' S ) -2- [5 '-(1-thia-2,3-diazol-5-ylthio) methyl-pyrrolidine-3'-ylthio] -6- (1-hydroxyethyl) -1- Preparation of Methylcarbafen-2-m-3-carboxylic Acid

(Step 1)

(3 S , 5 S Preparation of) -N-allyloxycarbonyl-5- (1-thia-2,3-diazol-5-ylthio) methyl-3-acetylthio pyrrolidine

(3 S, 5 S) -N- allyloxycarbonyl-5-iodo was added methyl-3-acetylthio pyrrolidine 3.7 g (10 mmol) where 1.4 g (10 mmol) in 100 mL of acetone in the 5-mercapto 1-thia-2,3-diazine sodium was added and then heated to reflux for 5 hours. 100 mL of water and 100 mL of ether were added to the reaction mixture, followed by extraction. The ether layer was evaporated to dryness. 3.3 g (92%) of (3 S , 5 S ) -N-allyloxycarbonyl-5- (1- Thia-2,3-diazol-5-ylthio) methyl-3-acetylthio pyrrolidine was obtained.

IR (neat, NaCl) 1694, 1402, 1120 cm ⁻¹ ; ¹ H NMR (CDCl ₃ ) δ 8.49, 8.33 (s, 1H), 5.76-5.67 (m, 1H), 5.13-5.00 (m, 2H), 4.37 (br s, 2H), 4.01 (br d, 1H, J = 7.1 Hz), 3.89-3.83 (m, 1H), 3.71 (quin, 1H, J = 7.4 Hz), 3.54-3.35 (m, 1H), 3.11-3.02 (m, 2H), 2.46-2.40 (m , 1H), 2.14 (s, 3H), 1.73-1.67 (m, 1H); ¹³ C NMR (CDCl ₃ ) δ 193.66, 193.52, 153.77, 152.39, 145.29, 145.23, 131.97, 118.29, 117.11, 65.67, 65.45, 55.77, 55.16, 52.09, 40.58, 39.25, 38.45, 38.18, 36.31, 36.26 29.97; MS (CI) m / z 360 (M + l) ⁺ , 358, 332, 318, 274, 242, 228, 200, 198, 172, 152, 142, 108, 77, 59; HRMS calcd for C ₁₃ H ₁₈ N ₃ O ₃ S ₃ (M + 1) ⁺ 360.0510, found 360.0508.

(Step 2)

Preparation of (3S, 5S) -N-allyloxycarbonyl-5- (1-thia-2,3-diazol-5-ylthio) methyl-3-mercapto pyrrolidine

Of 3.1 g (8.6 mmol) in 30 mL of methanol and carbon dioxide dihydrochloride mixed solution of 20 mL (3 S, 5 S ) -N- allyloxycarbonyl-5- (1-thiazol-2,3-diazole -5 -Ylthio) methyl-3-acetylthio pyrrolidine was added, cooled to 0 ° C, and slowly 5 mL of 2N NaOH aqueous solution was added slowly. The reaction solution was stirred at 0 ° C. for 30 minutes, and then 50 mL of water and 50 mL of carbon dichloride were added to extract the organic layer. Evaporation of the organic layer is dried of 2.7 g (99%) (3 S, 5 S) -N- allyloxycarbonyl-5- (1-thiazol-2,3-oxadiazole-5-ylthio) methyl-3 Mercapto pyrrolidine was obtained.

IR (neat, NaCl) 2548 cm ⁻¹ ; ¹ H NMR (CDCl ₃ ) δ 8.50, 8.34 (s, 1H), 5.78-5.70 (m, 1H), 5.15-5.03 (m, 2H), 4.47 (d, 2H, J = 14.2 Hz), 4.00-3.95 (m, 1H), 3.86-3.81 (m, 1H), 3.57-3.40 (m, 1H), 3.27-3.14 (m, 2H), 3.05-2.98 (m, 1H), 2.51-2.43 (m, 1H) , 1.75 (d, 1H, J = 6.4 Hz), 1.70-1.64 (m, 1H); ¹³ C NMR (CDCl ₃ ) δ 153.70, 152.69, 145.31, 145.22, 132.01, 118.32, 117.14, 65.77, 65.42, 56.27, 55.63, 40.94, 40.336, 40.22, 39.56, 33.99, 33.58; MS (CI) m / z 318 (M + l) ⁺ 232, 200, 186, 172, 152, 142, 119, 99, 82. 59; HRMS calcd for C ₁₁ H ₁₆ N ₃ O ₂ S ₃ (M + 1) ⁺ 318.0405, found 318.0407.

(Step 3)

(One R , 5 S , 6 S , 8 R , 3 ' S , 5 ' S ) -2- [N-allyloxycarbonyl-5 '-(1-thia-2,3-diazol-5-ylthio) methyl-pyrrolidine-3'-ylthio] -6- (1- Preparation of hydroxyethyl) -1-methylcarbaphen-2-m-3-carboxylic acid allyl ester

(1 R , 5 S , 6 S , 8 R ) -6- (1-hydroxyethyl) -1-methyl-2-diphenylphosphoryloxycarbafen-2-emcarboxylic acid allyl ester 1 g (2 mmol) in 15 mL of acetonitrile, followed by 0.42 mL (2.4 mmol) of diisopropylethylamine and (2S, 4S) -N-allyloxycarbonyl-2- (1-thia-2,3-diazole-5 634 mg (2 mmol) of -ylthio) methyl-4-mercapto pyrrolidine were added sequentially at 0 ° C. After stirring the reaction solution for 5 hours, the solvent was distilled under reduced pressure and the remaining residue was purified by column chromatography to obtain 0.72 g (64%) of (1 R , 5 S , 6 S , 8 R , 3 ' S , 5' S). ) -2- [N-allyloxycarbonyl-5 '-(1-thia-2,3-diazol-5-ylthio) methyl-pyrrolidine-3'-ylthio] -6- (1- Hydroxyethyl) -1-methylcarbaphen-2-m-3-carboxylic acid allyl ester was obtained.

IR (KBr) 3448, 1770, 1698 cm ⁻¹ ; ¹ H NMR (CDCl ₃ ) δ 8.64, 8.47 (s, 1H), 5.97-5.84 (m, 2H), 5.42-5.18 (m, 4H), 4.80-4.73 (m, 1H), 4.66-4.52 (m, 3H), 4.21-4.13 (m, 3H), 4.04-3.90 (m, 1H), 3.70-3.51 (m, 2H), 3.33-3.20 (m, 4H), 2.55 (br s, 1H), 2.61-2.58 (m, 1H), 1.99-1.89 (m, 1H), 1.28 (d, 3H, J = 5.7 Hz), 1.20 (d, 3H, J = 7.2 Hz); ¹³ C NMR (CDCl ₃ ) δ 172.52, 160.16, 154.11, 152.74, 147.19, 147.07, 145.79, 145.70, 145.66, 132.15, 131.89, 131.28, 126.01, 119.27, 118.35, 118.10, 66.47, 66.32, 65.65, 65.65 56.39, 56.28, 55.99, 55.46, 54.68, 54.56, 43.42, 40.98, 40.93, 40.29, 39.62, 36.15, 35.58, 21.68, 21.62, 16.72, 16.66; MS (FAB) m / z 567 (M + l) ⁺ 522, 481, 449, 395, 339, 284, 251, 198, 152, 136, 68, 41, 39; HRMS calcd for C ₂₄ H ₃₁ N ₄ O ₆ S ₃ (+1) ⁺ 567.1406, found 567.1404.

(Step 4)

(One R , 5 S , 6 S , 8 R , 3 ' S , 5 ' S ) -2- [5 '-(1-thia-2,3-diazol-5-ylthio) methyl-pyrrolidine-3'-ylthio] -6- (1-hydroxyethyl) -1- Preparation of Methylcarbafen-2-m-3-carboxylic Acid

(1 R , 5 S , 6 S , 8 R , 3 ' S , 5' S ) -2- [N-allyloxycarbonyl-5 '-(1-thia-2,3-diazol-5-yl Thio) methyl-pyrrolidine-3'-ylthio] -6- (1-hydroxyethyl) -1-methylcarbaphen-2-m-3-carboxylic acid allyl ester dichloride 560 mg (1 mmol) After dissolving in 20 mL of carbon carbide and lowering the temperature to 0 ° C., 50 mg of Pd (PPh ₃ ) ₄ and 0.05 mL of water were added thereto. 0.7 mL (2.5 mmol) of n- Bu ₃ SnH was slowly added thereto, stirred for 1 hour, and extracted with 50 mL of distilled water. The water layer was washed with carbon dichloride and ethyl acetate, purified by column chromatography using diion HP-20 resin, and then lyophilized to obtain the above (1 R , 5 S , 6 S , 8 R , 3 ' S , 5 ' S ) -2- [5'-(1-thia-2,3-diazol-5-ylthio) methyl-pyrrolidine-3'-ylthio] -6- (1-hydroxyethyl)- 230 mg (52%) of 1-methylcarbafen-2-m-3-carboxylic acid were obtained.

IR (KBr) 3388, 1754, 1592 cm ⁻¹ ; ¹ H NMR (D ₂ O) δ 8.87 (s, 1H), 4.35-4.27 (m, 2H), 4.14-4.01 (m, 3H), 3.81-3.60 (m, 3H), 3.54-3.38 (m, 3H ), 2.96-2.85 (m, 1H, C4′-H), 1.96-1.85 (m, 1H), 1.35 (d, 3H, J = 6.3 Hz), 1.27 (d, 3H, J = 7.2 Hz); MS (FAB) m / z 443 (M + l) ⁺ 415, 383, 329, 307, 289, 246, 200, 154, 136, 107, 89, 68, 39, 23; HRMS calcd for C ₁₇ H ₂₃ N ₄ O ₄ S ₃ (M + 1) ⁺ 443.0881, found 443.0878.

<Example 2> (One R , 5 S , 6 S , 8 R , 3 ' S , 5 ' S ) -2- [5 '-(1- (2-dimethylaminoethyl) -1,2,3,4-tetrazol-5-ylthio) methyl-pyrrolidine-3'-ylthio] -6- Preparation of (1-hydroxyethyl) -1-methylcarbafen-2-m-3-carboxylic acid

(Step 1)

(3 S , 5 S Preparation of) -N-allyloxycarbonyl-5- [1- (2-dimethylaminoethyl) -1,2,3,4-tetrazol-5-ylthio] methyl-3-acetylthio pyrrolidine

(3 S, 5 S) -N- allyloxycarbonyl-5-iodo-3-methyl put acetylthio pyrrolidine 3.7 g (10 mmol) 1.73 g (10 mmol) in 100 mL of acetone to this 5-mercapto-1- (2-dimethylaminoethyl) -1,2,3,4-tetrazole was added and then heated to reflux for 5 hours. To the reaction mixture 100 mL of water and 100 mL of ethyl acetate into the extraction when dried and evaporated and the organic layer of 3.8 g (92%) (3 S, 5 S) -N- allyloxycarbonyl-5- [1 - (2-dimethylaminoethyl) -1,2,3,4-tetrazol-5-ylthio] methyl-3-acetylthio pyrrolidine was obtained.

¹ H NMR (CDCl ₃ ) δ 5.95-5.83 (m, 1H), 5.30-5.17 (m, 2H), 4.56 (d, 2H, J = 4.7 Hz), 4.27 (t, 2H, J = 6.3 Hz), 4.09-4.04 (m, 1H), 3.90-3.50 (m, 3H), 3.19 (dd, 1H, J = 8.2, 11.2 Hz), 2.73 (t, 2H), 2.53 (br s, 1H), 2.30 (s , 3H), 2.23 (s, 6H), 1.95-1.88 (m, 1H).

(Step 2)

(One R , 5 S , 6 S , 8 R , 3 ' S , 5 ' S ) -2- [N-allyloxycarbonyl-5 '-(1- (2-dimethylaminoethyl) -1,2,3,4-tetrazol-5-ylthio) methyl-pyrrolidine-3' Preparation of -ylthio] -6- (1-hydroxyethyl) -1-methylcarbaphen-2-m-3-carboxylic acid allyl ester

2.07 g (5 mmol) of (3 S , 5 S ) -N-allyloxycarbonyl-5- [1- (2-dimethylaminoethyl) -1, in 30 mL of methanol and 20 mL of carbon dichloride solution 2,3,4-tetrazol-5-ylthio] methyl-3-acetylthio pyrrolidine was added thereto, cooled to 0 ° C., and 3 mL of a 2N NaOH aqueous solution was slowly added thereto. The reaction solution was stirred at 0 ° C. for 30 minutes, and then 50 mL of water and 50 mL of carbon dichloride were added to extract the organic layer. Evaporation of the organic layer is dried of 1.78 g (96%) (3 S, 5 S) -N- allyloxycarbonyl-5- [1- (2-dimethylaminoethyl) -1, 2,3,4-tetrazol -5-ylthio] methyl-3-mercapto pyrrolidine was obtained. This compound was used directly in the next reaction without purification.

(1 R , 5 S , 6 S , 8 R ) -6- (1-hydroxyethyl) -1-methyl-2-diphenylphosphoryloxycarbafen-2-emcarboxylic acid allyl ester 1 g (2 mmol) in 15 mL of acetonitrile solvent, followed by 0.42 mL (2.4 mmol) of diisopropylethylamine and (3 S , 5 S ) -N-allyloxycarbonyl-5- [1- (2-dimethylaminoethyl) 744 mg (2 mmol) of -1,2,3,4-tetrazol-5-ylthio] methyl-3-mercapto pyrrolidine were added sequentially at 0 ° C. After stirring the reaction solution for 5 hours, the solvent was distilled under reduced pressure and the remaining residue was purified by column chromatography to obtain 0.94 g (63%) of (1 R , 5 S , 6 S , 8 R , 3 ' S , 5' S). ) -2- [N-allyloxycarbonyl-5 '-(1- (2-dimethylaminoethyl) -1,2,3,4-tetrazol-5-ylthio) methyl-pyrrolidine-3' -Ylthio] -6- (1-hydroxyethyl) -1-methylcarbaphen-2-m-3-carboxylic acid allyl ester was obtained.

¹ H NMR (CDCl ₃ ) δ 5.98-5.87 (m, 2H), 5.45-5.20 (m, 4H), 4.79-4.57 (m, 4H), 4.40-4.00 (m, 6H), 3.84-3.57 (m, 3H), 3.36-3.22 (m, 2H), 2.75 (t, 2H, J = 6.3 Hz), 2.67-2.55 (m, 1H), 2.25 (s, 6H), 2.03-1.90 (m, 1H), 1.33 (d, 3H, J = 6.1 Hz), 1.24 (d, 3H, J = 7.4 Hz).

(Step 3)

(One R , 5 S , 6 S , 8 R , 3 ' S , 5 ' S ) -2- [5 '-(1- (2-dimethylaminoethyl) -1,2,3,4-tetrazol-5-ylthio) methyl-pyrrolidine-3'-ylthio] -6- Preparation of (1-hydroxyethyl) -1-methylcarbafen-2-m-3-carboxylic acid

(1 R , 5 S , 6 S , 8 R , 3 ' S , 5' S ) -2- [N-allyloxycarbonyl-5 '-(1- (2-dimethylaminoethyl) -1,2, 3,4-tetrazol-5-ylthio) methyl-pyrrolidine-3'-ylthio] -6- (1-hydroxyethyl) -1-methylcarbafen-2-m-3-carboxylic acid 620 mg (1 mmol) of allyl ester were dissolved in 20 mL of carbon dichloride, and the temperature was lowered to 0 ° C., followed by 50 mg of Pd (PPh ₃ ) ₄ and 0.05 mL of water. 0.7 mL (2.5 mmol) of n- Bu ₃ SnH was slowly added thereto, stirred for 1 hour, and extracted with 50 mL of distilled water. The water layer was washed with carbon dichloride and ethyl acetate, purified by column chromatography using diion HP-20 resin, and then lyophilized to obtain the above (1 R , 5 S , 6 S , 8 R , 3 ' S , 5 ' S ) -2- [5'-(1- (2-dimethylaminoethyl) -1,2,3,4-tetrazol-5-ylthio) methyl-pyrrolidine-3'-ylthio]- 270 mg (55%) of 6- (1-hydroxyethyl) -1-methylcarbafen-2-m-3-carboxylic acid were obtained.

¹ H NMR (D ₂ O) δ4.72 (t, 2H, J = 6.1 Hz), 4.30-4.23 (m, 2H), 4.11-3.98 (m, 2H), 3.88-3.56 (m, 3H), 3.50 -3.31 (m, 5H), 2.87-2.73 (m, 1H), 2.71 (s, 6H), 1.86-1.77 (m, 1H), 1.32 (d, 3H, J = 6.4 Hz), 1.25 (d, 3H , J = 7.1 Hz).

<Example 3> (One R , 5 S , 6 S , 8 R , 3 ' S , 5 ' S ) -2- [5 '-(1- (2-trimethylammoniumethyl) -1,2,3,4-tetrazol-5-ylthio) methyl-pyrrolidine-3'-ylthio] -6 -(1-hi Preparation of Doxyethyl) -1-methylcarbafen-2-m-3-carboxylic acid salt

(1 R , 5 S , 6 S , 8 R , 3 ' S , 5' S ) -2- [N-allyloxycarbonyl-5 '-(1- (2-dimethylaminoethyl) -1,2, 3,4-tetrazol-5-ylthio) methyl-pyrrolidine-3'-ylthio] -6- (1-hydroxyethyl) -1-methylcarbafen-2-m-3-carboxylic acid 310 mg (0.5 mmol) of allyl ester were dissolved in 10 mL of acetone, the temperature was lowered to 0 ° C., and 0.12 mL (2 mmol) of CH ₃ I was added. The reaction solution was slowly stirred to room temperature, stirred for 7 hours, and then distilled under acetone solvent under reduced pressure to yield pale yellow crystals. The crystals were washed with ethyl acetate and 370 mg (97%) of (1 R , 5 S , 6 S). , 8 R , 3 ' S , 5' S ) -2- [N-allyloxycarbonyl-5 '-(1- (2-trimethylammoniumethyl) -1,2,3,4-tetrazol-5 -Ilthio) methyl-pyrrolidine-3'-ylthio] -6- (1-hydroxyethyl) -1-methylcarbafen-2-m-3-carboxylic acid allyl ester iodine salt was obtained.

(1 R , 5 S , 6 S , 8 R , 3 ' S , 5' S ) -2- [N-allyloxycarbonyl-5 '-(1- (2-trimethylammoniumethyl) -1,2 , 3,4-tetrazol-5-ylthio) methyl-pyrrolidine-3'-ylthio] -6- (1-hydroxyethyl) -1-methylcarbafen-2-m-3-carboxyl 380 mg (0.5 mmol) of the acid allyl ester iodine salt was dissolved in 15 mL of carbon dichloride, and the temperature was lowered to 0 ° C., followed by addition of 25 mg of Pd (PPh ₃ ) ₄ and 0.03 mL of water. 0.35 mL (1.25 mmol) of n- Bu ₃ SnH was slowly added thereto, stirred for 1 hour, and extracted with 50 mL of distilled water. The water layer was washed with carbon dichloride and ethyl acetate, purified by column chromatography using diion HP-20 resin, and then lyophilized to obtain the above (1 R , 5 S , 6 S , 8 R , 3 ' S , 5 ' S ) -2- [5'-(1- (2-trimethylammoniumethyl) -1,2,3,4-tetrazol-5-ylthio) methyl-pyrrolidine-3'-ylthio] 90 mg (35%) of -6- (1-hydroxyethyl) -1-methylcarbafen-2-m-3-carboxylic acid salt was obtained.

^OneH NMR (D₂O) δ 4.99 (t, 2H,J= 6.9 Hz), 4.30-4.21 (m, 2H), 4.07 (t, 2H,J= 6.9 Hz), 3.95-3.69 (m, 3H), 3.50-3.32 (m, 2H), 3.32 (s, 9H), 2.93-2.85 (m, 1H), 1.97-1.89 (m, 1H), 1.32 ( d, 3H,J= 6.3 Hz), 1.25 (d, 3H,J= 7.0 Hz). MS (relative intensity) (FAB)m / z1023 [(M + 1-HI)⁺]², 640 (M + 1)⁺(0.6), 512 (M + 1-HI)⁺(35.4), 425 (4.1), 307 (18.4), 289 (10.3), 269 (9.1), 188 (12), 154 (79.5), 128 (base peak), 107 (16.4), 58 (31.9), 39 (6.77); HRMS calcd for C₁₈H₂₅N₄O₄S₃(M + 1-HI)⁺512.2114, found 512.2117.

<Example 4-Example 17>

The compounds of Examples 4 to 17 were obtained according to the preparation methods of Examples 1, 2, and 3, and the chemical formulas and confirmed results of these compounds are shown in Table 1 below.

Chemical formula and compound identification analysis results of the compounds of the present invention Example Chemical formula Substituent Compound analysis result One - - Description in specification 2 Y -CH ₂ CH ₂ N (CH ₃ ) ₂ Description in specification 3 ^{_{-CH 2 CH 2 N + (CH}} 3) 3 I - Description in specification 4 -CH ₃ IR (KBr) 3390 (CO ₂ H), 1760 (β-lactam), 1574 cm ⁻¹ ; ¹ H NMR (D ₂ O) δ 4.30-4.20 (m, 3H), 4.19-4.06 (m, 1H), 4.05 (s, 3H, CH ₃ ), 3.90-3.68 (m, 3H), 3.52-3.47 ( m, 2H), 3.45-3.35 (m, 1H, C1-H), 2.96-2.85 (m, 1H, C4'-H), 1.98-1.91 (m, 1H, C4'-H), 1.32 (d, 3H, J = 6.4 Hz, C H ₃ CHOH), 1.25 (d, 3H, J = 7.2 Hz, 1β-CH ₃ ); ¹³ C NMR (D ₂ O) δ 171.99, 163.00, 149.23, 133.29, 129.27, 60.46, 54.44, 54.21, 51.30, 47.76, 37.78, 35.08, 30.16, 29.24, 29.00, 15.50, 11.19; MS (FAB) m / z (relative intensity) 441 (M + 1) ⁺ (40), 311 (9), 286 (9), 232 (14), 198 (28), 158 (32), 114 (52 ), 82 (base peak), 68 (90), 43 (24), 30 (23); HRMS calcd for C ₁₇ H ₂₅ N ₆ O ₄ S ₂ (M + 1) ⁺ 441.1379, found 441.1368.

Example Chemical formula Substituent Compound analysis result 5 Y -CH ₂ CH ₂ OH IR (KBr) 3406 (CO ₂ H), 1752 (β-lactam), 1586 cm ⁻¹ ; _{^{1 H NMR (D 2 O)}} δ 4.56 (t, 2H, J = 4.7 Hz, ArC H 2 - C H 2), 4.30-4.18 (m, 3H), 4.11-4.04 (m, 3H), 3.90-3.69 (m, 3H), 3.52-3.46 (m, 2H), 3.45-3.34 (m, 1H, C1-H), 2.94-2.85 (m, 1H, C4'-H), 1.97-1.89 (m, 1H, C4'-H), 1.32 (d, 3H, J = 6.3 Hz, C H ₃ CHOH), 1.24 (d, 3H, J = 7.2 Hz, 1β-CH ₃ ); ¹³ C NMR (D ₂ O) δ 171.02, 163.01, 148.78, 133.29, 129.31, 60.50, 54.70, 54.52, 54.25, 51.34, 47.79, 45.63, 37.83, 35.10, 30.20, 29.28, 15.53, 11.23; MS (FAB) m / z (relative intensity) 471 (M + 1) ⁺ (30), 307 (21), 289 (11), 228 (7), 154 (base peak), 136 (65), 107 ( 20), 89 (17), 68 (12), 39 (7); HRMS calcd for C ₁₈ H ₂₇ N ₆ O ₅ S ₂ (M + 1) ⁺ 471.1484, found 471.1484. 6 ¹ H NMR (D ₂ O) δ 7.75-7.67 (m, 5H, Ar-H), 4.30-4.22 (m, 3H), 4.09-4.06 (m, 1H), 3.92-3.85 (m, 1H), 3.78 -3.67 (m, 2H), 3.51-3.34 (m, 3H) 2.90-2.86 (m, 1H, C4'-H), 1.95-1.88 (m, 1H, C4'-H), 1.30 (d, 3H, J = 6.1 Hz, C H ₃ CHOH), 1.23 (d, 3H, J = 7.1 Hz, 1β-CH ₃ ).

Example Chemical formula Substituent Compound analysis result 7 Y ¹ H NMR (D ₂ O) δ 8.87 (d, 2H, J = 5.4 Hz, Ar-H), 7.90-7.88 (m, 2H, Ar-H), 4.32-4.25 (m, 3H), 4.14-3.70 (m, 4H), 3.52-3.46 (m, 2H), 3.44-3.37 (m, 1H, C1-H), 2.95-2.90 (m, 1H, C4'-H), 2.00-1.92 (m, 1H, C4′-H), 1.33 (d, 3H, J = 6.6 Hz, C H ₃ CHOH), 1.25 (d, 3H, J = 7.3 Hz, 1β-CH ₃ ). 8 -CH ₂ CH ₂ SO ₂ N (CH ₃ ) ₂ ¹ H NMR (D ₂ O) δ 4.92-4.84 (m, 2H, CH ₂ -C H ₂ ), 4.30-4.00 (m, 4H), 3.88-3.68 (m, 5H), 3.31-3.45 (m, 2H ), 3.44-3.32 (m, 1H, C1-H), 2.86 (s, 6H, N (CH ₃ ) ₂ ), 2.93-2,82 (m, 1H, C4'-CH ₂ ), 1.98-1.85 ( m, 1H, C 4′-CH ₂ ), 1.31 (d, 3H, J = 6.4 Hz, C H ₃ CHOH), 1.20 (d, 3H, J = 7.2 Hz, 1β-CH ₃ ). 9 -CH ₂ CH ₂ SO ₂ NHCH ₃ ¹ H NMR (D ₂ O) δ 4.91-4.84 (m, 2H, CH ₂ -C H ₂ ), 4.31-4.03 (m, 4H), 3.91-3.72 (m, 5H), 3.51-3.46 (m, 3H ), 2.97-2.85 (m, 1H, C4'-CH ₂ ), 2.76 (s, 3H, NCH ₃ ), 1.99-1.89 (m, 1H, C4'-CH ₂ ), 1.33 (d, 3H, J = 6.4 Hz, C H ₃ CHOH), 1.25 (d, 3H, J = 7.2 Hz, 1β-CH ₃ ).

Example Chemical formula Substituent Compound analysis result 10 Y -CH ₂ CH ₂ CONH ₂ IR (KBr) 3420 (CO ₂ H), 1752 (β-lactam), 1676 cm ⁻¹ ; _{^{1 H NMR (D 2 O)}} δ 4.65 (t, 2H, J = 6.5 Hz, ArC H 2 - C H 2), 4.31-4.08 (m, 4H), 3.92-3.70 (m, 3H), 3.52-3.48 (m, 2H), 3.43-3.38 (m, 1H, C1-H), 3.03 (t, 2H, J = 6.5 Hz, ArCH ₂ -C H ₂ ), 2.96-2.86 (m, 1H, C4'-H ), 1.98-1.90 (m, 1H, C 4′-H), 1.33 (d, 3H, J = 6.4 Hz, C H ₃ CHOH), 1.26 (d, 3H, J = 7.2 Hz, 1β-CH ₃ ); ¹³ C NMR (D ₂ O) δ 172.05, 170.18, 163.08, 143.38, 133.25, 129.39, 60.51, 54.54, 54.28, 51.35, 47.81, 39.29, 37.83, 35.13, 30.23, 29.27, 28.90, 15.53, 11.23; MS (FAB) m / z (relative intensity) 498 (M + 1) ⁺ (62), 307 (16), 289 (12), 256 (9), 255 (8), 154 (base peak), 136 ( 64), 114 (23), 107 (20), 89 (18), 68 (26); HRMS calcd for C ₁₉ H ₂₈ N ₇ O ₅ S ₂ (M + 1) ⁺ 498.1593, found 498.1595. 11 -CH ₂ CH ₂ CONHCH ₃ ¹ H NMR (D ₂ O) δ 4.66 (t, 2H, J = 6.4 Hz, ArC H ₂ - C H ₂ ), 4.30-4.05 (m, 4H), 3.93-3.84 (m, 1H), 3.79-3.70 (m, 3H), 3.54-3.35 (m, 3H), 2.97 (t, 2H, J = 6.4 Hz, ArCH ₂ -C H ₂ ), 3.00-2.85 (m, 1H, C4'-H), 2.70 ( s, 3H, NCH ₃ ), 1.99-1.88 (m, 1H, C4′-H), 1.33 (d, 3H, J = 6.2 Hz, C H ₃ CHOH), 1.26 (d, 3H, J = 7.2 Hz, 1β-CH ₃ ).

Example Chemical formula Substituent Compound analysis result 12 Y -CH ₂ CONHCH ₃ ¹ H NMR (D ₂ O) δ 5.27 (s, 2H, CH ₂ ), 4.72-4.02 (m, 4H), 3.86-3.66 (m, 3H), 3.48-3.45 (m, 2H), 3.41-3.34 ( m, 1H, C1-H), 2.91-2.81 (m, 1H, C4'-CH ₂ ), 2.81 (s, 3H, NCH ₃ ), 1.94-1.86 (m, 1H, C4'-CH ₂ ), 1.28 (d, 3H, J = 6.4 Hz, C H ₃ CHOH), 1.22 (d, 3H, J = 7.2 Hz, 1β-CH ₃ ). 13 -CH ₂ CON (CH ₃ ) ₂ ¹ H NMR (D ₂ O) δ 4.00 (s, 2H, CH ₂ ), 4.72-4.47 (m, 3H), 4.30-4.09 (m, 3H), 3.93-3.87 (m, 2H), 3.85-3.76 ( m, 1H, C1-H), 3.62 (s, 3H, NCH ₃ ), 3.44 (s, 3H, NCH ₃ ), 3.40-3.27 (m, 1H, C4'-CH ₂ ), 2.39-2.29 (m, 1H, C 4′-CH ₂ ), 1.74 (d, 3H, J = 6.4 Hz, C H ₃ CHOH), 1.66 (d, 3H, J = 7.3 Hz, 1β-CH ₃ ). 14 X -CH ₃ ¹ H NMR (D ₂ O) δ 8.44 (d, 1H, J = 5.3 Hz), 7.20 (d, 1H, J = 5.3 Hz), 4.26-4.12 (m, 3H), 4.06-4.02 (m, 1H) , 3.71-3.61 (m, 3H), 3.54-3.46 (m, 3H), 2.89-2.78 (m, 1H), 2.46 (br s, 3H), 1.98-1.89 (m, 1H), 1.28 (d, 3H , J = 6.2 Hz), 1.19 (d, 3H, J = 7.1 Hz).

Example Chemical formula Substituent Compound analysis result 15 X -CF ₃ ¹ H NMR (D ₂ O) δ 8.96 (d, 1H, J = 5.0 Hz, Ar-H), 7.71 (d, 1H, J = 5.0 Hz, Ar-H), 4.33-4.24 (m, 2H), 4.22-4.18 (m, 1H), 4.12-4.04 (m, 1H), 3.87-3.81 (m, 1H), 3.74-3.62 (m, 2H), 3.51-3.45 (m, 2H), 3.43-3.37 (m , 1H, C1-H), 2.96-2.84 (m, 1H, C4'-CH ₂ ), 2.01-1.91 (m, 1H, C4'-CH ₂ ), 1.34 (d, 3H, J = 6.2 Hz, C H ₃ CHOH), 1.25 (d, 3H, J = 7.4 Hz, 1β-CH ₃ ). 16 Z -CH ₃ ¹ H NMR (D ₂ O) δ 8.52 (s, 1H, Ar-H) 4.26-4.20 (m, 2H), 4.03-4.00 (m, 2H), 3.70-3.58 (m, 4H), 3.52-3.35 ( m, 5H), 2.82-2.75 (m, 1H, C4'-CH ₂ ), 1.89-1.79 (m, 1H, C4'-CH ₂ ), 1.28 (d, 3H, J = 6.4 Hz, C H ₃ CHOH ), 1.20 (d, 3H, J = 7.1 Hz, 1β-CH ₃ ).

Example Chemical formula Substituent Compound analysis result 17 - - IR (KBr) 3386 (CO ₂ H), 1752 (β-lactam), 1590 cm ⁻¹ ; ¹ H NMR (D ₂ O) δ 4.29-4.21 (m, 2H), 4.10-3.98 (m, 2H), 3.81-3.72 (m, 1H), 3.66-3.56 (m, 2H), 3.50-3.32 (m , 3H), 2.82-2.74 (m, 1H, C4'-H), 2.74 (s, 3H, Ar-CH ₃ ), 1.87-1.75 (m, 1H, C4'-H), 1.30 (d, 3H, J = 6.0 Hz, C H ₃ CHOH), 1.22 (d, 3H, J = 7.1 Hz, 1β-CH ₃ ); MS (relative intensity) (FAB) m / z 457 (M + 1) ⁺ 307 (26), 289 (13), 214 (6), 195 (3), 154 (base peak), 136 (6), 107 (19), 89 (16), 77 (15), 65 (7), 39 (6), 31 (2); HRMS calcd for C ₁₈ H ₂₅ N ₄ O ₄ S ₃ (M + 1) ⁺ 457.1038, found 457.1046.

Experimental Example 1 Antibacterial Activity Test

As the 1-beta-methylcarbapenem Gram-positive bacteria was used in the streptococci (Streptococcus) and Staphylococcus aureus (Staphylococcus) gram-negative bacteria as test organisms to determine the antimicrobial activity of the penem derivative of the present invention, Escherichia coli (Escherichia), Pseudomonas aeruginosa (Pseudomonas), salmonella (Salmonella), keurep when Ella bacteria (Klebsiella) and Enterobacteriaceae (Enterobacter) was used. After culturing the test strains in dilute agar medium, the compounds of the present invention were treated to show the minimum strain inhibition concentration in μg per ml and are shown in Table 2 below. Imiphenem and meropenem were used as a comparison group.

As a result of the minimum strain inhibition (MIC) test, the novel carbapenem of Example 1 having 1,2,3-thiadiazole heterocycle in the novel 1-betamethylcarbapenem derivative of the present invention was added to the standard strains except Pseudomonas aeruginosa. It can be seen that the antimicrobial activity of about 1 to 4 times improved. The novel carbapenem with the 1-methyltetrazole of Example 4, which has the simplest substituent at the N-1 position, shows excellent antimicrobial activity against all of the standard strains, about 1 to 31 times greater than imipenem, except for P. aeruginosa. It can be seen that the activity is improved by 1 to 4 times or more for the neem.

The novel carbapenem of Example 17 having a 1,3,4-thiadiazole heterocyclic substituent showed excellent antibacterial effects against imipenem and meropenem except three species of Pseudomonas aeruginosa. In particular, it showed better results for Staphylococcus aureus than imipenem, which has the highest activity among the existing carbapenem antibiotics, and improved the antibacterial activity of E. coli by about 8 to 50 times, resulting in a new 5'-heteroarylthiomethyl 1-betamethylcarbapenem derivatives substituted with pyrrolidin-3'-ylthio groups show the potential as novel antibacterial agents.

Minimum strain inhibition values of the other compounds are shown in Table 2 below.

Minimum Strain Inhibition Concentration for Standard Strains Minimum Inhibitory Concentration (㎍ / ml) Example Strain^One One 2 3 4 5 6 IPM ² MPM ³ S. pyogens 308A 0.007 0.013 0.025 0.004 0.007 0.007 0.007 0.013 S. pyogens 77A 0.004 0.007 0.013 <0.002 0.007 0.007 0.004 <0.002 S. faecium MD8b 3.125 3.125 6.25 6.25 6.25 3.125 1.563 12.5 S ^* . aureus SG511 0.025 0.049 0.098 0.025 0.098 0.049 0.025 0.098 S ^* . aureus 285 0.049 0.098 0.195 0.049 0.098 0.049 0.025 0.195 S ^* . aureus 503 0.013 0.025 0.049 0.025 0.049 0.025 0.013 0.098 E. coli 055 0.013 0.025 0.049 0.025 0.025 0.195 0.098 0.013 E. coli DC 0 0.013 0.049 0.098 0.025 0.025 0.391 0.098 0.025 E. coli DC 2 0.025 0.098 0.195 0.025 0.049 0.025 0.391 0.025 E. coli TEM 0.013 0.049 0.098 0.025 0.049 0.391 0.195 0.025 E. coli 1507E 0.013 0.049 0.098 0.025 0.025 0.391 0.195 0.025 P. aeruginosa 9027 1.563 3.125 0.781 0.781 1.563 50 0.781 0.195 P. aeruginosa 1592E 3.125 3.125 0.781 0.781 1.563 50 1.563 0.195 P. aeruginosa 1771 3.125 3.125 1.563 0.781 3.125 25 0.781 0.195 P. aeruginosa 1771M 0.195 0.195 0.195 0.195 0.195 3.125 0.195 0.049 S ^** . typhimurium 0.025 0.098 0.195 0.025 0.049 0.098 0.781 0.025 K. oxytoca 1082E 0.025 0.098 0.195 0.049 0.098 0.098 0.391 0.049 K. aerogenes 1522E 0.025 0.098 0.195 0.025 0.049 0.391 0.391 0.049 E ^* . cloacae P99 0.049 0.195 0.195 0.025 0.049 1.563 0.391 0.025 E ^* . cloacae 1321E 0.013 0.049 0.098 0.025 0.049 0.098 0.195 0.025 1. S .; Streptococcus, S ^* .; Staphylococcus, E .; Escherichia, P .; Pseudomonas, S ^** .; Salmonella, K .; Klebsiella, E ^* .; Enterobacter 2. Imipenem 3. Meropenem

Minimum Inhibitory Concentration (㎍ / ml) Example^One 7 8 9 10 11 IPM ² MPM ³ S. pyogens 308A 0.007 0.007 0.007 0.013 0.007 0.007 0.013 S. pyogens 77A 0.004 0.007 0.007 0.007 0.007 0.004 <0.002 S. faecium MD8b 3.125 6.25 3.125 3.125 6.25 1.563 12.5 S ^* . aureus SG511 0.049 0.098 0.098 0.098 0.098 0.025 0.098 S ^* . aureus 285 0.098 0.098 0.098 0.098 0.098 0.025 0.195 S ^* . aureus 503 0.049 0.025 0.025 0.025 0.049 0.013 0.098 E. coli 055 0.098 0.025 0.025 0.025 0.025 0.098 0.013 E. coli DC 0 0.391 0.025 0.013 0.025 0.025 0.098 0.025 E. coli DC 2 0.049 0.025 0.025 0.049 0.049 0.391 0.025 E. coli TEM 0.195 0.025 0.025 0.025 0.049 0.195 0.025 E. coli 1507E 0.195 0.025 0.025 0.025 0.025 0.195 0.025 P. aeruginosa 9027 50 6.25 3.125 1.563 1.563 0.781 0.195 P. aeruginosa 1592E 50 12.5 3.125 0.781 1.563 1.563 0.195 P. aeruginosa 1771 25 6.25 1.563 1.563 3.125 0.781 0.195 P. aeruginosa 1771M 0.781 0.391 0.391 0.195 0.391 0.195 0.049 S ^** . typhimurium 0.049 0.049 0.049 0.049 0.049 0.781 0.025 K. oxytoca 1082E 0.195 0.098 0.049 0.098 0.098 0.391 0.049 K. aerogenes 1522E 0.195 0.049 0.049 0.049 0.049 0.391 0.049 E ^* . cloacae P99 1.563 0.049 0.049 0.049 0.049 0.391 0.025 E ^* . cloacae 1321E 0.098 0.025 0.025 0.025 0.025 0.195 0.025 1. S .; Streptococcus, S ^* .; Staphylococcus, E .; Escherichia, P .; Pseudomonas, S ^** .; Salmonella, K .; Klebsiella, E ^* .; Enterobacter 2. Imipenem 3. Meropenem

Minimum Inhibitory Concentration (㎍ / ml) Example^One 12 13 14 16 17 IPM ² MPM ³ S. pyogens 308A 0.013 0.013 0.007 0.013 0.004 0.007 0.013 S. pyogens 77A 0.007 0.007 0.004 0.007 0.004 0.004 <0.002 S. faecium MD8b 6.25 6.25 6.25 3.125 0.781 1.563 12.5 S ^* . aureus SG511 0.195 0.195 0.049 0.049 0.025 0.025 0.098 S ^* . aureus 285 0.195 0.195 0.098 0.098 0.025 0.025 0.195 S ^* . aureus 503 0.098 0.049 0.025 0.025 0.007 0.013 0.098 E. coli 055 0.025 0.025 0.049 0.025 0.007 0.098 0.013 E. coli DC 0 0.025 0.025 0.049 0.025 0.007 0.098 0.025 E. coli DC 2 0.049 0.049 0.098 0.049 0.007 0.391 0.025 E. coli TEM 0.049 0.049 0.098 0.049 0.025 0.195 0.025 E. coli 1507E 0.049 0.049 0.098 0.049 0.013 0.195 0.025 P. aeruginosa 9027 1.563 3.125 25 1.563 3.125 0.781 0.195 P. aeruginosa 1592E 1.563 3.125 50 3.125 3.125 1.563 0.195 P. aeruginosa 1771 1.563 3.125 25 1.563 3.125 0.781 0.195 P. aeruginosa 1771M 0.391 0.391 6.25 0.195 0.195 0.195 0.049 S ^** . typhimurium 0.098 0.049 0.098 0.098 0.025 0.781 0.025 K. oxytoca 1082E 0.098 0.098 0.098 0.098 0.025 0.391 0.049 K. aerogenes 1522E 0.098 0.098 0.098 0.098 0.025 0.391 0.049 E ^* . cloacae P99 0.098 0.098 0.098 0.098 0.013 0.391 0.025 E ^* . cloacae 1321E 0.049 0.049 0.098 0.049 0.007 0.195 0.025 1. S .; Streptococcus, S ^* .; Staphylococcus, E .; Escherichia, P .; Pseudomonas, S ^** .; Salmonella, K .; Klebsiella, E ^* .; Enterobacter 2. Imipenem 3. Meropenem

Experimental Example 2 DHP-I Stability Test

The following experiment was conducted to determine the stability of the 1-betamethylbacapenem derivative of the present invention against DHP-I secreted by the kidney.

The DHP-I used in the experiment was partially separated from the pig kidney cortex, and the amount of enzyme capable of hydrolyzing the substrate in half at 30 ° C. for 30 minutes using imipenem as a substrate was used. . 50 μg / ml concentration of drug and 1 unit of DHP-I were added to 1 ml of MOPS buffer and incubated at 30 ° C. to measure OD values at wavelengths of 299 nm at 0.5, 1, 2, and 4 time periods.

The results of the above experiment are shown in Table 3 by setting the _half- life (t _1/2 ) of meropenem for the DHP-I enzyme to 1.00 and calculating the relative stability upon hydrolysis of each drug. The comparative group was carried out on the same compound as Experimental Example 1.

Relative Stability for DHP-I Enzymes Example DHP-I susceptibility Example DHP-I susceptibility One 1.67 10 0.92 2 0.88 11 0.91 3 1.35 12 0.86 4 0.88 13 0.86 5 0.96 14 1.22 6 NT 16 0.93 7 0.98 17 NT 8 0.72 IPM ¹ 0.19 9 NT MPM ² 1.00 Imipenem 2. Meropenem NT: Not Tested

The stability of the novel 1-betamethylcarbapenem of the present invention against the DHP-I enzyme was much higher than that of imipenem having no 1β-methyl group and showed equal or superior stability within experimental error compared to meropenem. . It should be noted that the compounds of Examples 1, 3 and 14 showed 1.67 times, 1.35 times and 1.22 times superior DHP-I stability, respectively, compared to meropenem. This result suggests that bioavailability will be more favorable than meropenem in vivo.

Experimental Example 3 Acute Toxicity in Parenteral Administered Rats

On the other hand, the following experiment was carried out to determine the acute toxicity of the compound of Formula 1.

Acute toxicity test was performed using 6 week-old SPF SD rats. The compound of Example 1 was suspended in 1 ml of saline and administered intravenously to the tails of the two rats at doses of 1000 mg / kg and 2000 mg / kg. After administration of the test substance, mortality, clinical symptoms, and changes in body weight were observed. Hematological and hematological examinations were performed. Necropsy was performed to observe abdominal and thoracic organ abnormalities. As a result, there were no clinical symptoms or deaths in all animals treated with the test substance, and no toxicity change was observed in weight change, blood test, blood biochemistry test, autopsy findings, etc. As a result, the compound of Formula 1 did not show a toxic change in rats up to 2000 mg / kg, and the parenteral administration minimum dose (LD ₅₀ ) was determined to be a safe substance of 2 g / kg or more.

As described above, the 1-betamethylcarbapenem derivative substituted with the 5'-heteroarylthiomethylpyrrolidine-3'-ylthio group represented by Formula 1 of the present invention is excellent for both Gram-positive bacteria and Gram-negative bacteria. It exhibits antimicrobial activity and is stable against the DHP-I enzyme secreted by the kidney, and thus has excellent bioavailability, and thus may be usefully used as an antibacterial agent.

Claims (11)

1-betamethylcarbapenem derivative represented by the following formula (1) and a pharmaceutically acceptable salt thereof. Formula 1 In the above formula, R is ego, X is trifluoromethyl or an alkyl group of C _{1 to} C ₃ , Y is substituted with an alkyl group of C ₁ ~C ₃ straight or branched chain aliphatic alkyl group a, C ₁ ~C ₃ alkyl group is substituted with one or two C ₁ ~C ₃ of sulfone amido group, C ₁ ~C ₃ of the or an unsubstituted C ₁ ~C ₃ alkyl group of the carboxylic bore not shown, C ₁ ~C ₃ alkyl group of hydroxy, C ₁ ~C a C ₁ ~C ₃ alkyl group substituted with _{3-amino-alkyl} group or an aryl group, Z represents an alkyl group of C ₁ ~C _3. The method of claim 1 wherein in formula (I) according to FIG characterized in that the ethyl sulfone amido group is methyl sulfone amido group or a sulfonamido dimethyl the C ₁ ~C ₃ alkyl group, one or two C ₁ ~C ₃ with the substitution of 1-betamethylcarbapenem derivatives represented and pharmaceutically acceptable salts thereof. The C ₁ -C ₃ carboamidoalkyl group substituted or unsubstituted with a C ₁ -C ₃ alkyl group is a carboamidoethyl group, methylcarboamidoethyl group or methylcarboamidomethyl group. 1-betamethylcarbapenem derivative represented by Formula 1 and pharmaceutically acceptable salts thereof. The 1-betamethylcarbapenem derivative represented by the formula (1), wherein the aryl group is a phenyl group or a pyridine group, and a pharmaceutically acceptable salt thereof. The 1-betamethylcarbapenem derivative represented by Formula 1 is 1) (1 R , 5 S , 6 S , 8 R , 3 ' S , 5' S ) -2- [5 '-(1-thia-2,3-diazol-5-ylthio) methyl-pi Ralidin-3'-ylthio] -6- (1-hydroxyethyl) -1-methylcarbafen-2-m-3-carboxylic acid, 2) (1 R , 5 S , 6 S , 8 R , 3 ' S , 5' S ) -2- [5 '-(1- (2-dimethylaminoethyl) -1,2,3,4-tetra Sol-5-ylthio) methyl-pyrrolidine-3'-ylthio] -6- (1-hydroxyethyl) -1-methylcarbafen-2-m-3-carboxylic acid, 3) (1 R , 5 S , 6 S , 8 R , 3 ' S , 5' S ) -2- [5 '-(1- (2-trimethylammoniumethyl) -1,2,3,4- Tetrazol-5-ylthio) methyl-pyrrolidine-3'-ylthio] -6- (1-hydroxyethyl) -1-methylcarbafen-2-m-3-carboxylic acid salt, 4) (1 R , 5 S , 6 S , 8 R , 3 ' S , 5' S ) -2- [5 '-(1-methyl-1,2,3,4-tetrazol-5-ylthio ) Methyl-pyrrolidine-3'-ylthio] -6- (1-hydroxyethyl) -1-methylcarbafen-2-m-3-carboxylic acid, 5) (1 R , 5 S , 6 S , 8 R , 3 ' S , 5' S ) -2- [5 '-(1- (2-hydroxyethyl) -1,2,3,4-tetra Sol-5-ylthio) methyl-pyrrolidine-3'-ylthio] -6- (1-hydroxyethyl) -1-methylcarbafen-2-m-3-carboxylic acid, 6) (1 R , 5 S , 6 S , 8 R , 3 ' S , 5' S ) -2- [5 '-(1-phenyl-1,2,3,4-tetrazol-5-ylthio ) Methyl-pyrrolidine-3'-ylthio] -6- (1-hydroxyethyl) -1-methylcarbafen-2-m-3-carboxylic acid, 7) (1 R , 5 S , 6 S , 8 R , 3 ' S , 5' S ) -2- [5 '-(1- (pyridin-4-yl) -1,2,3,4-tetra Sol-5-ylthio) methyl-pyrrolidine-3'-ylthio] -6- (1-hydroxyethyl) -1-methylcarbafen-2-m-3-carboxylic acid, 8) (1 R , 5 S , 6 S , 8 R , 3 ' S , 5' S ) -2- [5 '-(1- (2-dimethylsulfonamidoethyl) -1,2,3,4 -Tetrazol-5-ylthio) methyl-pyrrolidine-3'-ylthio] -6- (1-hydroxyethyl) -1-methylcarbafen-2-m-3-carboxylic acid, 9) (1 R , 5 S , 6 S , 8 R , 3 ' S , 5' S ) -2- [5 '-(1- (2-methylsulfonamidoethyl) -1,2,3,4 -Tetrazol-5-ylthio) methyl-pyrrolidine-3'-ylthio] -6- (1-hydroxyethyl) -1-methylcarbafen-2-m-3-carboxylic acid, 10) (1 R , 5 S , 6 S , 8 R , 3 ' S , 5' S ) -2- [5 '-(1- (2-carboamidoethyl) -1,2,3,4- Tetrazol-5-ylthio) methyl-pyrrolidine-3'-ylthio] -6- (1-hydroxyethyl) -1-methylcarbafen-2-m-3-carboxylic acid, 11) (1 R , 5 S , 6 S , 8 R , 3 ' S , 5' S ) -2- [5 '-(1- (2-methylcarboamidoethyl) -1,2,3,4 -Tetrazol-5-ylthio) methyl-pyrrolidine-3'-ylthio] -6- (1-hydroxyethyl) -1-methylcarbafen-2-m-3-carboxylic acid, 12) (1 R , 5 S , 6 S , 8 R , 3 ' S , 5' S ) -2- [5 '-(1- (methylcarboamidomethyl) -1,2,3,4-tetra Sol-5-ylthio) methyl-pyrrolidine-3'-ylthio] -6- (1-hydroxyethyl) -1-methylcarbafen-2-m-3-carboxylic acid, 13) (1 R , 5 S , 6 S , 8 R , 3 ' S , 5' S ) -2- [5 '-(1- (dimethylcarboamidomethyl) -1,2,3,4-tetra Sol-5-ylthio) methyl-pyrrolidine-3'-ylthio] -6- (1-hydroxyethyl) -1-methylcarbafen-2-m-3-carboxylic acid, 14) (1 R , 5 S , 6 S , 8 R , 3 ' S , 5' S ) -2- [5 '-(4-methylpyrimidin-2-ylthio) methyl-pyrrolidine-3' -Ylthio] -6- (1-hydroxyethyl) -1-methylcarbafen-2-m-3-carboxylic acid, 15) (1 R , 5 S , 6 S , 8 R , 3 ' S , 5' S ) -2- [5 '-(4-trifluoromethylpyrimidin-2-ylthio) methyl-pyrrolidine- 3'-ylthio] -6- (1-hydroxyethyl) -1-methylcarbafen-2-m-3-carboxylic acid, 16) (1 R , 5 S , 6 S , 8 R , 3 ' S , 5' S ) -2- [5 '-(1-methyl-1,3,4-triazol-5-ylthio) methyl -Pyrrolidine-3'-ylthio] -6- (1-hydroxyethyl) -1-methylcarbafen-2-m-3-carboxylic acid, or 17) (1 R , 5 S , 6 S , 8 R , 3 ' S , 5' S ) -2- [5 '-(2-methyl-1-thia-3,4-diazol-5-ylthio 1) -Methyl-pyrrolidine-3'-ylthio] -6- (1-hydroxyethyl) -1-methylcarbafen-2-m-3-carboxylic acid Betamethylcarbapenem derivatives and pharmaceutically acceptable salts thereof. 1) reacting carbapenem intermediate (III) with thiol derivative (II) in the presence of a base in a suitable solvent to prepare a protected carbapenem derivative (IV) (step 1), and 2) Deprotected reaction of the protected carbapenem derivative (IV) obtained in step 1 to prepare a 1-betamethyl carbapenem derivative (I) (1) characterized in that consisting of Method for preparing betamethylcarbapenem derivatives. Scheme 1 In Scheme 1, R is as defined in Formula 1, R 'is a carboxy protecting group. 7. The method of claim 6 wherein the base in step 1 consists of trimethylamine, triethylamine, diisopropylethylamine, 2,6-lutidine, picoline, N, N -dimethylaniline, pyridine, 4-dimethylaminopyridine Method for producing a 1-betamethyl carbapenem derivative represented by the formula (1) characterized in that selected from the group. Thiol derivative represented by the following formula (2) used to prepare a 1-betamethyl carbapenem derivative represented by the formula (1) of claim 1. Formula 2 In the above formula, R is ego, X is trifluoromethyl or an alkyl group of C _{1 to} C ₃ , Y is substituted with an alkyl group of C ₁ ~C ₃ straight or branched chain aliphatic alkyl group a, C ₁ ~C ₃ alkyl group is substituted with one or two C ₁ ~C ₃ of sulfone amido group, C ₁ ~C ₃ of the or an unsubstituted C ₁ ~C ₃ alkyl group of the carboxylic bore not shown, C ₁ ~C ₃ alkyl group of hydroxy, C ₁ ~C a C ₁ ~C ₃ alkyl group substituted with _{3-amino-alkyl} group or an aryl group, Z represents an alkyl group of C ₁ ~C _3. Condensation reaction of the iodine compound represented by formula (V) with a mercapto heteroaromatic compound represented by formula (VI) in the presence of a base to prepare a thioacetyl-based compound represented by formula (VII), and 2) A process for producing a thiol derivative represented by the formula (2), comprising the step (step 3) of obtaining a thiol compound (II) by hydrolyzing the thioacetyl compound (VII) obtained in step 1 above. Scheme 2 Wherein R and R 'are as defined in the formula (2). 10. The method of claim 9, wherein the base of step 1 is selected from the group consisting of potassium carbonate or sodium carbonate as the alkali base. A pharmaceutical composition for an antimicrobial agent comprising the 1-betamethylcarbapenem derivative of claim 1 or a pharmaceutically acceptable salt thereof as an active ingredient.