US 4,123,547 AGrant
Thienamycin Sulfoxide and Sulphone
Issue Date:1978-10-31
•3 Claims
Abstract
Thienamycin sulfoxide (I, n=1), Thienamycin sulfone (I, n=2), and their pharmaceutically acceptable salts are disclosed to be useful as antibiotics: ##STR1## Also disclosed are processes for the preparation of such compounds, pharmaceutical compositions comprising such compounds, and methods of treatment comprising administering such compounds and compositions when an antibiotic effect is indicated.
Metadata
Assignee
- Merck & Co., Inc.
Inventors
- Burton G. Christensen
- Edward Walton
Application Information
Application Number:US 8336202
Filing Date:1977-09-15
Priority Date:1976-03-16
Art Unit:122
Classifications
IPC:
C07D48704A61K 3140
Field of Search:
260424326.31274
Patent Drawings
This patent does not have any drawings.
Description
The following examples further illustrate, but do not limit the product, process, compositional or method of treatment aspects of the present invention.
EXAMPLE 1
Preparation of Thienamycin Sulfoxide
Step A: Preparation of O, N-bis Trimethylsilyl-Thienamycin trimethylsilyl ester, Th(TMS).sub.3 ##STR5##
Thienamycin (36.7 mg., 0.135 mmole) is suspended in 20 ml. tetrahydrofuran (THF) under a nitrogen atmosphere and is concentrated to 5 ml; hexamethyldisilazane (0.5 ml) and trimethylchlorosilazane (150 .mu.l) is added. The mixture is reacted for 20 minutes at 25.degree. C., with vigorous stirring. The suspension is then centrifuged to remove ammonium chloride. The supernatant is evaporated to an oil under a nitrogen stream to provide O, N-bis trimethylsilylthienamycin trimethylsilyl ester.
Step B: Preparation of Thienamycin sulfoxide ##STR6##
The Th(TMS).sub.3 from Step A is dissolved in 3 ml of tetrahydrofuran and treated with a solution of 23.4 mg of m-chloroperbenzoic acid in 1 ml. of tetrahydrofuran. The reaction solution is concentrated to dryness and the residue is dissolved in 5 ml of 0.1N pH 7.0 sodium phosphate buffer and kept at 5.degree. C. for 24 hours to remove the trimethylsilyl blocking groups. The resulting solution comprising thienamycin sulfoxide and exhibiting an absorption maximum at 282 nm is evaporated to dryness to provide the desired product, thienamycin sulfoxide.
Following the procedure of Example 1 except that the two equivalents of m-chloroperbenzoic acid (46.8 mg) are employed, rather than the one equivalent of Example 1, thienamycin sulphone is obtained.
EXAMPLE 2
Preparation of Thienamycin Sulfoxide
A solution of 36.7 mg (0.135 mmole) of thienamycin in 2 ml of water is cooled to 5.degree. C and treated with a solution of 26.2 mg of the sodium salt of m-chloroperbenzoic acid and the mixture is stirred until the oxidant is consumed. (negative test with KI-starch test paper). The reaction mixture is acidified to pH 3 with dilute hydrochloric acid and extracted with three 4 ml portions of ether to remove the m-chloroperbenzoic acid. The aqueous phase is neutralized to pH 7 with dilute sodium hydroxide. The salts are removed from the aqueous phase by passing it through a column of 50 ml of XAD resin and eluting with distilled water. The fractions containing the thienamycin sulfoxide are pooled and freeze-dried to give a residue of thienamycin sulfoxide.
Similarly, when any isomeric form of II or mixture of isomers of II is substituted, in equivalent amount, for the thienamycin of Examples 1 and 2, there is obtained the corresponding antibiotic sulfoxide or sulphone of II.
EXAMPLE 3
Preparation of Thienamycin Sulfoxide ##STR7## Aqueous sodium hypochlorite (0.75 ml of a 5.25% solution) is added dropwise over 45 sec. to a stirred solution of thienamycin (92.5 mg) in water (75 ml) at 25.degree. C. The pH climbs from 5.2 to 10.0. After 1 min, the pH is adjusted to 7.0 with 0.1N hydrochloric acid (0.33 ml); UV analysis of the reaction mixture shows that 75% of the original UV absorption is retained. Electrophoresis (20 min, 2KV, pH 7) shows a continuous bioactive streak from the origin to +5 cm (monoanion range). The reaction mixture is concentrated in vacuo at 25.degree. C to 1.5 ml and charged onto a Dowex 50 column (100 ml, sodium form). The column is eluted with water while monitoring the effluent by UV and refractive index (RI). After the first RI (colored) band is rejected, the product is collected as a second RI colorless band. The product solutions gives a UV maximum at 289 nm, an origin bioactive spot by electrophoresis, and two close eluting bands in 3:1 ratio by HPLC, both more polar than thienamycin. Lyophilization of this solution provides an amorphous powder (33 mg) whose NMR spectrum is in accord with thienamycin sulfoxide.
EXAMPLE 4
Preparation of Thienamycin Sulfoxide ##STR8##
STEP A: N-(p-nitrobenzyloxycarbonyl)thienamycin p-nitrobenzyl ester ##STR9## Thienamycin (140 mg, 0.51 mmol) is dissolved in ice-cold H.sub.2 O (35 ml) and the solution is treated with NaHCO.sub.3 (428 mg, 5.1 mmol). Dioxane (35 ml) is then added with stirring and ice-bath cooling. After 3 mins, a solution of p-nitrobenzyl chloroformate (165 mg, 0.765 mmol) in dioxane (2 ml) is added dropwise over 2 mins. The resulting mixture is stirred in the cold for 10 mins and then extracted with ice-cold Et.sub.2 O (2.times.20 ml). The aqueous phase is separated, layered with ice-cold EtOAc (35 ml), and acidified to pH 2.3 with 1M H.sub.2 SO.sub.4 while vigorously stirring in an ice-bath. The layers are separated and the aqueous portion extracted with more cold EtOAc (2.times.5 ml). The combined EtOAc extracts are washed with ice-cold brine and then extracted thoroughly with 0.05N aq. LiOH (10 ml). The LiOH extract is rotary evaporated to remove EtOAc and then lyophilized to provide crude N-(p-nitrobenzyloxycarbonyl) thienamycin lithium salt (288 mg) as a yellow solid.
A portion of the crude lithium carboxylate (250 mg) and p-nitrobenzyl bromide (373 mg, 1.73 mmol) in anhydrous HMPA (2.65 ml) are stirred at room temperature (25.degree. C) for 105 mins. The mixture is diluted with EtOAc (60 ml), washed with H.sub.2 O (2.times.50 ml), 5% NaHCO.sub.3 (25 ml), H.sub.2 O (2.times.25 ml), and brine (25 ml), dried with MgSO.sub.4, filtered, and evaporated in vacuo(i.v.) to a yellow solid (423 mg). This material is triturated with Et.sub.2 O to remove excess p-nitrobenzyl bromide and the remaining crystals are filtered off and dried i.v. to yield N-(p-nitrobenzyloxycarbonyl)thienamycin p-nitrobenzyl ester (126 mg) as a yellow solid: mp 163.5- 165.degree.; ir (Nujol mull) 1773 and 1690 cm.sup.-1 ; nmr (DMSO-d.sub.6) .delta. 1.15(d,3, CH.sub.3), 2.8-3.6(m,7,CH.sub.2, SCH.sub.2, NCH.sub.2, H.sub.6), 4.0 (m,2,H5,H8), 5.22 (s,2, NCO.sub.2 CH.sub.2 Ar), 5.40(ABq, 2, CO.sub.2 CH.sub.2 Ar), 7.70(m,ArH), and 8.27(m,ArH). [Relative to the above text, Et.sub.2 O symbolizes diethylether and EtOAc is ethylacetate.]
STEP B: Preparation of N-(p-nitrobenzyloxycarbonyl)thienamycin p-nitrobenzyl ester S-oxide ##STR10## N-(p-nitrobenzyloxycarbonyl) thienamycin p-nitrobenzyl ester (117.3 mg, 0.20 mmol) is dissolved in anhydrous tetrahydrofuran (6.0 ml) and the solution is stirred under a nitrogen atmosphere with ice-bath cooling. A solution of 85% m-chloroperbenzoic acid (44.7 mg, 0.22 mmol) in anhydrous methylene chloride (2.0 ml) is added dropwise over 8 mins to the solution. The resulting solution is stirred in the cold an additional 12 mins, then diluted with ethyl acetate (20 ml), washed with 5% sodium bicarbonate (2 .times. 10 ml) and brine, dried with magnesium sulfate, filtered, and concentrated under reduced pressure to provide the crude sulfoxide (125 mg) as a pale yellow solid. The crude product is triturated with ethyl acetate (2 .times. 2 ml) and ethyl ether (2 .times. 4 ml) and dried in vacuo to yield substantially pure N-(p-nitrobenzyloxycarbonyl) thienamycin p-nitrobenzyl ester S-oxide (57 mg) as an off-white powder: mp 142.degree.-143.degree.; ir (nujol) 3450, 3315, 1780, 1695, 1520, and 1347 cm.sup.-1 ; uv (dioxane) 266 (.epsilon. 21,200) and 325 (sh, .epsilon. 6150); nmr (CDCl.sub.3, 300 MHz).delta. 1.36 (d, CH.sub.3), 3.23 (m, SCH.sub.2), 3.32 (m, CH.sub.2), 3.42 (dd, H.sub.6), 3.78(m, NCH.sub.2), 4.30(m, H8), 4.41(dt, H5), 5.24(ABq, NCO.sub.2 CH.sub.2 Ar), 5.39(ABq, CO.sub.2 CH.sub.2 Ar), 7.55(d, 2, ArH), 7.68(d, 2, ArH), 8.25(d, 2, ArH) and 8.28 (d, 2, ArH).
STEP C: Preparation of Thienamycin S-oxide ##STR11## N-(p-nitrobenzyloxycarbonyl)thienamycin p-nitrobenzyl ester s-oxide (25 mg) is dissolved in dioxane (3.0 ml) and the solution is treated with 10% palladium on powdered charcoal (25 mg), ethanol (0.25 ml), 1M dipotassium hydrogen phosphate (0.05 ml), and deionized water (1.75 ml). The resulting mixture is hydrogenated on a Parr shaker for 1 hr. The pressure drops from 50 psi to 45 psi during the course of the reduction. The catalyst is removed by centrifugation and washed with 0.1M pH 7 phosphate buffer (1 ml) and water (1 ml). The combined superantants are washed with ethyl acetate (3 .times. 3 ml), concentrated in vacuo to 1 ml, and charged onto a Dowex 50-X 4 column (1.4 .times. 20 cm, sodium form). The column is eluted with deionized water; 5.5 ml fractions being collected every 4.0 mins. The progress of the chromatograph is monitored by UV and HPLC. Fractions 5 and 6 are combined to give 11 ml of a solution containing thienamycin S-oxide. An aliquot (0.2 ml) of this solution diluted to 2.0 ml with water gives a UV spectrum having A=0.63 at 289 nm. The combined fractions 5-6 are brought to pH 6.8 with 1N hydrochloric acid, concentrated in vacuo to 3 ml, and lyophilized to afford thienamycin S-oxide as a light brown, amorphous powder: ir(nujol) 1765 cm.sup.-1 ; UV(H.sub.2 O) 289 nm; nmr(D.sub.2 O, 300 MHz) .delta. 1.29(d, 3, CH.sub.3), 3.24 and 3.26 (d of ABq, CH.sub.2), 3.5 (m, SCH.sub.2 and NCH.sub.2), 3.67(d of d,H6), 4.28(d of q, H8) and 4.42(d of t, H5).
EXAMPLE 5
Preparation of Pharmceutical Compositions
One such unit dosage form consists in mixing 120 mg. of thienamycin sulfoxide with 20 mg of lactose and 5 mg of magnesium stearate and placing the 145 mg mixture into a No. 3 gelatin capsule. Similarly, by employing more active ingredient and less lactose, other dosage forms can be put up in No 3 gelatin capsules and should it be necessary to mix more than 145 mg of ingredients together, larger capsules such as compressed tablets and pills can also be prepared. The following examples are illustrative of the preparation of pharmaceutical formulations:
The active ingredient is blended with the dicalcium phosphate, lactose and about half of the cornstarch. The mixture is then granulated with a 15% cornstarch paste (6 mg.) and rough-screened. It is dried at 45.degree. C., and screened again through No. 16 screens. The balance of the cornstarch and the magnesium stearate is added and the mixture is compressed into tablets, approximately 0.5 inch in diameter each weighing 800 mg.
The active ingredient in the above formulations may be administered alone or in combination with other biologically active ingredients as, for example, with other antibacterial agents such as lincomycin, a penicillin, streptomycin, novobiocin, gentamicin, neomycin, colistin and kanamycin, or with other therapeutic agents such as probenecid.
Claims
What is claimed is:
1. A compound having the structural formula: ##STR12## wherein n is an integer selected from 1 or 2 and the non-toxic, pharmaceutically acceptable salts thereof.
2. The compound according to claim 1 wherein n = 1.
3. An antibacterial pharmaceutical composition comprising, in unitary dosage form, a therapeutically effective amount of a compound according to claim 1 and a pharmaceutical carrier therefor.