Crotonyl alcohol cassic acid ester with antibacterial activity and a method of preparing the same

Abstract

A compound having the formula (I): ##STR00001##
(I) is disclosed. A method of preparing the compound of formula (I) is also disclosed.

Claims

1. A compound having the following formula (I): ##STR00004##

2. A method of preparing the compound of formula (I) of claim 1, comprising: reacting the compound of formula (II) with the compound of formula (III) to obtain the compound of formula (I): ##STR00005##

3. The method of claim 2, wherein the reaction of the compound of formula (II) with the compound of formula (III) comprises the following steps: placing the compound of formula (II) and the compound of formula (III), in a molar ratio of 1:1 to 1:1.3, in a reactor; adding an organic solvent and a catalytic amount of EDC (1-ethyl-3-(3-dimethylaminopropyl) carbamide) under nitrogen atmosphere to obtain a reaction mixture; and heating the reaction mixture at 50-75 C. for 1-4 hours; and purifying the crude product on a silica gel fresh chromatography column with petroleum ether and ethyl acetate as an eluent to obtain the compound of formula (I).

4. The method of claim 3, wherein the organic solvent is toluene, tetrahydrofuran or acetonitrile.

5. The method of claim 4, wherein the organic solvent is acetonitrile.

6. The method of claim 3, wherein the molar ratio of the compound of formula (II) and the compound of formula (III) is 1:1.1.

7. The method of claim 3, wherein the reaction mixture is heated at 75 C.

8. The method of claim 3, wherein the reaction mixture is heated for 4 hours.

9. The method of claim 3, wherein the eluent is petroleum ether:ethyl acetate=1:3.

10. The method of claim 2, wherein the reaction of the compound of formula (II) with the compound of formula (III) comprises the following steps: placing the compound of formula (II), a catalyst, and an ionic liquid in a reactor under nitrogen atmosphere, the catalyst being 12-molybdosilicic acid hydrate (H.sub.6Mo.sub.12O.sub.41Si); adding the compound of formula (III) to the reactor to form a reaction mixture; heating the reaction mixture at 25-50 C. for 5-10 hours; placing the reaction mixture in a separating funnel to separate a crude product; purifying the crude product by recrystallization in methanol to obtain the compound of formula (I); and recycling the ionic liquid.

11. The method of claim 10, wherein the ionic liquid is 1-butyl-3-methylimidazolium tetrafluoroborate ([BMIM][BF.sub.4]).

12. The method of claim 10, wherein the compound of formula (II) and the compound (III) have a molar ratio of 1:1 to 1:1.3.

13. The method of claim 12, wherein the molar ratio of the compound of formula (II) and the compound of formula (III) is 1:1.1.

14. The method of claim 10, wherein the reaction mixture is heated at 25 C.

15. The method of claim 10, wherein the reaction mixture is heated for 8 hours.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) The accompanying drawings, which are included to provide a further understanding of the invention and are incorporated in and constitute a part of this specification, illustrate embodiments of the invention and together with the description serve to explain the principles of the invention.

(2) In the drawings:

(3) FIG. 1 shows the results of in vitro antibacterial activity of crotonyl alcohol cassic acid ester against drug-resistant bacteria MARS 18-222.

(4) FIG. 2 shows the results of in vitro antibacterial activity of cassic acid against drug-resistant bacteria MARS 18-222.

(5) FIG. 3 shows the results of in vitro antibacterial activity of crotonyl alcohol against drug-resistant bacteria MARS 18-222.

(6) FIG. 4 shows the results of in vitro antibacterial activity of crotonyl alcohol cassic acid ester against drug-resistant bacteria MARS 18-575.

(7) FIG. 5 shows the results of in vitro antibacterial activity of cassic acid against drug-resistant bacteria MARS 18-575.

(8) FIG. 6 shows the results of in vitro antibacterial activity of crotonyl alcohol against drug-resistant bacteria MARS 18-575.

DETAILED DESCRIPTION OF THE ILLUSTRATED EMBODIMENTS

(9) Reference will now be made in detail to embodiments of the present invention, example of which is illustrated in the accompanying drawings. The following examples illustrate the present invention, but the present invention is not limited to the following examples.

Example 1

Preparation of (E)-but-2-en-1-yl 4,5-dihydroxy-9,10-dioxo-9,10-dihydroanthracene-2-carboxylate (compound of formula I)

(10) In a 250 mL three-necked flask, 200.0 mg (0.7 mmol) of cassic acid and 134.0 mg (0.7 mmol) EDC (1-ethyl-3-(3-dimethylaminopropyl)carbodiimide) were dissolved in 90 mL of acetonitrile under nitrogen gas atmosphere. 55.6 mg (0.77 mmol) of crotonyl alcohol was dissolved in 10 mL of acetonitrile, and slowly added dropwise to the reaction liquid by a separatory funnel. After the completion of the dropwise addition, the temperature was raised to 75 C., and the reaction was carried out for 4 hours. Thin layer chromatography was used to track the reaction to completion, heating was stopped, and the protective device was removed. The concentrated solution was washed in water, extracted with ethyl acetate, dried and concentrated, and a crude product was obtained. The crude product was further purified by silica gel column chromatography with petroleum ether:ethyl acetate=3:10 as eluent, and the eluent was concentrated under reduced pressure and dried to obtain the title compound, 172.6 mg, a yield of 72.88%.

(11) .sup.1H-NMR (400 MHz, DMSO-d.sup.6) (ppm): 7.89 (2H, d), 7.81 (1H, s), 7.45 (1H, s), 7.06 (1H, d), 5.88 (2H, t), 5.31 (2H, s), 4.57 (2H, s), 1.98 (3H, s); .sup.13C-NMR (400 MHz, DMSO-d.sup.6) (ppm): 185.0, 179.5, 164.3, 160.8, 159.7, 134.2, 133.5, 129.5, 129.3, 129.1, 120.1, 116.3, 60.8, 17.3.

Example 2

Preparation of (E)-but-2-en-1-yl 4,5-dihydroxy-9,10-dioxo-9,10-dihydroanthracene-2-carboxylate

(12) In a 250 mL three-necked flask, 200.0 mg (0.7 mmol) of cassic acid and 134.0 mg (0.7 mmol) EDC were dissolved in 90 mL of toluene under nitrogen gas atmosphere. 55.6 mg (0.77 mmol) of crotonyl alcohol was dissolved in 10 mL of toluene, and slowly added dropwise to the reaction liquid by a separatory funnel. After the completion of the dropwise addition, the temperature was raised to 60 C., and the reaction was carried out for 3 hours. Thin layer chromatography was used to track the reaction to completion, heating was stopped, and the protective device was removed. The concentrated solution was washed in water, extracted with ethyl acetate, dried and concentrated, and a crude product was obtained. The crude product was further purified by silica gel column chromatography with petroleum ether:ethyl acetate=3:10 as eluent, and the eluent was concentrated under reduced pressure and dried to obtain the title compound, 132.8 mg, a yield of 56.07%.

Example 3

Preparation of (E)-but-2-en-1-yl 4,5-dihydroxy-9,10-dioxo-9,10-dihydroanthracene-2-carboxylate

(13) In a 250 mL three-necked flask, 200.0 mg (0.7 mmol) of cassic acid and 134.0 mg (0.7 mmol) EDC were dissolved in 90 mL of tetrahydrofuran under nitrogen gas atmosphere. 55.6 mg (0.77 mmol) of crotonyl alcohol was dissolved in 10 mL of tetrahydrofuran, and slowly added dropwise to the reaction liquid by a separatory funnel. After the completion of the dropwise addition, the temperature was raised to 50 C., and the reaction was carried out for 4 hours. Thin layer chromatography was used to track the reaction to completion, heating was stopped, and the protective device was removed. The concentrated solution was washed in water, extracted with ethyl acetate, dried and concentrated, and a crude product was obtained. The crude product was further purified by silica gel column chromatography with petroleum ether:ethyl acetate=3:10 as eluent, and the eluent was concentrated under reduced pressure and dried to obtain the title compound, 137.9 mg, a yield of 58.23%.

Example 4

Preparation of (E)-but-2-en-1-yl 4,5-dihydroxy-9,10-dioxo-9,10-dihydroanthracene-2-carboxylate

(14) In a 250 mL three-necked flask, 200.0 mg (0.7 mmol) of cassic acid and 134.0 mg (0.7 mmol) EDC were dissolved in 90 mL of toluene under nitrogen gas atmosphere. 60.6 mg (0.84 mmol) of crotonyl alcohol was dissolved in 10 mL of toluene, and slowly added dropwise to the reaction liquid by a separatory funnel. After the completion of the dropwise addition, the temperature was raised to 65 C., and the reaction was carried out for 2 hours. Thin layer chromatography was used to track the reaction to completion, heating was stopped, and the protective device was removed. The concentrated solution was washed in water, extracted with ethyl acetate, dried and concentrated, and a crude product was obtained. The crude product was further purified by silica gel column chromatography with petroleum ether:ethyl acetate=3:10 as eluent, and the eluent was concentrated under reduced pressure and dried to obtain the title compound, 146.5 mg, a yield of 61.86%.

Example 5

Preparation of (E)-but-2-en-1-yl 4,5-dihydroxy-9,10-dioxo-9,10-dihydroanthracene-2-carboxylate

(15) In a 250 mL three-necked flask, 200.0 mg (0.7 mmol) of cassic acid and 134.0 mg (0.7 mmol) EDC were dissolved in 90 mL of acetonitrile under nitrogen gas atmosphere. 60.6 mg (0.84 mmol) of crotonyl alcohol was dissolved in 10 mL of acetonitrile, and slowly added dropwise to the reaction liquid by a separatory funnel. After the completion of the dropwise addition, the temperature was raised to 60 C., and the reaction was carried out for 3 hours. Thin layer chromatography was used to track the reaction to completion, heating was stopped, and the protective device was removed. The concentrated solution was washed in water, extracted with ethyl acetate, dried and concentrated, and a crude product was obtained. The crude product was further purified by silica gel column chromatography with petroleum ether:ethyl acetate=3:10 as eluent, and the eluent was concentrated under reduced pressure and dried to obtain the title compound, 159.8 mg, a yield of 67.47%.

Example 6

Preparation of (E)-but-2-en-1-yl 4,5-dihydroxy-9,10-dioxo-9,10-dihydroanthracene-2-carboxylate

(16) In a 250 mL three-necked flask, 200.0 mg (0.7 mmol) of cassic acid and 134.0 mg (0.7 mmol) EDC were dissolved in 90 mL of tetrahydrofuran under nitrogen gas atmosphere. 55.6 mg (0.77 mmol) of crotonyl alcohol was dissolved in 10 mL of tetrahydrofuran, and slowly added dropwise to the reaction liquid by a separatory funnel. After the completion of the dropwise addition, the temperature was raised to 55 C., and the reaction was carried out for 4 hours. Thin layer chromatography was used to track the reaction to completion, heating was stopped, and the protective device was removed. The concentrated solution was washed in water, extracted with ethyl acetate, dried and concentrated, and a crude product was obtained. The crude product was further purified by silica gel column chromatography with petroleum ether:ethyl acetate=3:10 as eluent, and the eluent was concentrated under reduced pressure and dried to obtain the title compound, 154.3 mg, a yield of 65.22%.

Example 7

Preparation of (E)-3,4-dihydroxyphenethyl 3-(4-methoxyphenyl)acrylate

(17) In a 250 mL three-necked flask, 200.0 mg (0.7 mmol) of cassic acid, 55.6 mg (0.77 mmol) of crotonyl alcohol and 12.0 mg (0.007 mmol) silicomolybdic acid were dissolved in 100 mL of 1-butyl-3-methylimidazolium tetrafluoroborate under nitrogen atmosphere. After full dissolution, the temperature was raised to 25 C. and the reaction was carried out for 8 hours. Thin layer chromatography was used to track the reaction to completion, heating was stopped, and the protective device was removed. The reaction mixture system was allowed to separate into layers to give a crude product. The crude product was recrystallized with 50 mL methanol and dried to obtain the title compound, 194.8 mg, a yield of 82.25%.

Example 8

Preparation of (E)-3,4-dihydroxyphenethyl 3-(4-methoxyphenyl)acrylate

(18) In a 250 mL three-necked flask, 200.0 mg (0.7 mmol) of cassic acid, 55.6 mg (0.77 mmol) of crotonyl alcohol and 12.0 mg (0.007 mmol) silicomolybdic acid were dissolved in 100 mL of 1-butyl-3-methylimidazolium tetrafluoroborate under nitrogen atmosphere. After full dissolution, the temperature was raised to 50 C. and the reaction was carried out for 4 hours. Thin layer chromatography was used to track the reaction to completion, heating was stopped, and the protective device was removed. The reaction mixture system was allowed to separate into layers to give a crude product. The crude product was recrystallized with 50 mL methanol and dried to obtain the title compound, 178.7 mg, a yield of 75.45%.

Example 9

Antibacterial Activity Test of the Compounds of Formula I

(19) The minimal inhibitory concentration (MIC) of the compounds as determined by microbroth dilution method with gentamicin, cefazolin sodium and ceftriaxone sodium as positive control.

(20) The experimental strains included methicillin-resistant Gram-positive bacteria: methicillin-resistant Staphylococcus aureus MRSA 18-222, 18-575; multiple drug-resistant Gram-negative bacteria: vancomycin-resistant enterococci VRE 18-80,18-94, multidrug-resistant Pseudomonas aeruginosa MDR-PA 18-1774,18-202, carbapenem-resistant Acinetobacter baumannii CR-AB 18-183,18-560. All the experimental strains were donated by Huashan Hospital affiliated to Fudan University (Institute of antibiotics, Fudan University) and used after routine identification.

(21) Preparation of Test Strains:

(22) Preparation of MHB medium: 20.0 g MHB medium was added to 1 L distilled water, boiled until completely dissolved, packed in conical bottles and sterilized at 121 C. for 15 min.

(23) The experimental strain was cultured to the logarithmic growth phase: under aseptic condition, the experimental strain was inoculated into 100 mL MHB medium and incubated in a constant temperature and humidity incubator at 37 C. for 20-22 hours.

(24) Preparation of storage solution: weigh the sample to be tested, dissolve it with 1% DMSO solution, prepare a storage solution with a concentration of 2560 g/mL, weigh a positive reference substance, dissolve it with aseptic distilled water, and configure a storage solution with a concentration of 2560 g/mL.

(25) Preparation of bacterial suspension: under aseptic condition, the experimental strains cultured to logarithmic growth phase were adjusted to 0.5 MCF turbidity standard with MHB medium and diluted according to 1:10, and the bacterial suspension with concentration of 106 CFU/mL was prepared for standby.

(26) Dilution of storage solution and inoculation of experimental strain: under aseptic condition, the storage solution was diluted to 256 g/mL solution. Take a sterile 96-well plate, add 200 L MHB medium to the 12th well, and add 100 L MHB medium to each well. Add 100 L of positive control solution to the first well, mix well, and suck 100 L from it and discard. Add 100 L of the compound sample solution to the second well, mix well, and then pipette 100 L to the third well. After mixing, pipette 100 L to the fourth well, and dilute to the 11th well in this way. Finally, 100 L was pipetted from the 11th well and discarded. The 12th hole was the growth control without drugs. So far, the concentration of the positive reference substance is 128 g/mL, the concentrations of the sample solution are 128, 64, 16, 8, 4, 2, 1, 0.5, 0.25 g/mL respectively. Then, 10L of the prepared bacterial suspension is added to each well, so that the final concentration of the bacterial liquid in each well is 510.sup.5 CFU/mL.

(27) Incubation: Cover the 96-well plate inoculated with the experimental strains, and incubate in a constant temperature and humidity box at 37 C. for 20-22 hours.

(28) Interpretation of the MIC endpoint: The concentration that can completely inhibit the growth of bacteria in a 96-well plate under a black background is the lowest inhibitory concentration of the sample against the bacteria.

(29) In FIGS. 1-10, the twelve wells represent twelve groups, from left to right, positive, 128 g/mL, 64 g/mL, 32 g/mL, 16 g/mL, 8 g/mL, 4 g/mL, 2 g/mL, 1 g/mL, 0.25 g/mL, 0.0625 g/mL, Negative. FIG. 1 shows the in vitro antibacterial activity of crotonyl alcohol cassic acid ester against drug-resistant bacteria MARS 18-222. FIG. 2 shows the in vitro antibacterial activity of cassic acid against drug-resistant bacteria MARS 18-222. FIG. 3 shows the in vitro antibacterial activity of crotonyl alcohol against drug-resistant bacteria MARS 18-222. FIG. 4 shows the in vitro antibacterial activity of crotonyl alcohol cassic acid ester against drug-resistant bacteria MARS 18-575. FIG. 5 shows the in vitro antibacterial activity of cassic acid against drug-resistant bacteria MARS 18-575. FIG. 6 shows the in vitro antibacterial activity of crotonyl alcohol against drug-resistant bacteria MARS 18-575. The results are shown in Table 1.

(30) TABLE-US-00001 TABLE 1 Minimum bacteriostatic concentration of test drug and positive drug (ug .Math. mL.sup.1) Strain MRSA VRE MDR-PA CR-AB Sample 18-222 18-575 18-80 18-94 18-174 18-202 18-183 18-560 Crotonyl alcohol 4 4 >128 >128 >128 >128 >128 >128 cassic acid ester Gentamicin 128 2 0.0625 >128 0.0625 0.0625 >128 >128 Cefazolin sodium >128 >128 32 >128 8 128 >128 >128 Ceftriaxone sodium >128 >128 8 >128 128 16 >128 >128 Cassic acid >128 >128 >128 >128 >128 >128 >128 >128 Crotonyl alcohol >128 >128 >128 >128 >128 >128 >128 >128

(31) According to the experimental results of FIG. 1-6 and Table 1, cassic acid and crotonyl alcohol had no inhibitory effect on drug-resistant bacteria, while crotonyl alcohol cassic acid ester showed a strong inhibitory effect on drug-resistant Gram-positive bacteria MRSA (MIC=4 g/mL), which was stronger than that of positive control drugs. In summary, the crotonyl alcohol cassic acid of the invention can be used as an antibacterial candidate for methicillin-resistant Staphylococcus aureus of Gram-positive bacteria, and further preclinical research can be carried out.