Abstract
Coptidis rhizome (CR) is a widely used herbal medicine that contains protoberberine-type alkaloids. CR extract exhibits various pharmacologic activities. A previous study reported the isolation of Rhodococcus sp. strain BD7100 as a berberine (BBR)-utilizing bacterium, and the BBR-degradation pathway has been investigated. When we incubated strain BD7100 cells with CR extract, the number of viable cells declined with the degradation of components in the CR extract, and the culture broth exhibited antibacterial activity against strain BD7100. These results suggest that CR extract cultured in the presence of strain BD7100 contains one or more antibacterial agents. In this study, we isolated coptirhoquinone A (1) from CR extract incubated with strain BD7100 in Luria–Bertani (LB) medium, and the structure was elucidated using NMR and MS analysis. We also report the total synthesis and antimicrobial activities of 1 against bacteria, fungi, and Pythium sp.
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Introduction
Coptidis rhizome (CR) is the dried rhizome of plants of the genus Coptis, such as C. japonica Makino and C. chinensis Franch. CR is widely used as a herbal medicine to relieve abdominal pain and diarrhea in traditional Chinese medicine and Japanese Kampo [1, 2]. Previous studies reported that CR extract and traditional medicines containing CR exhibit antimicrobial, antimalarial, anti-inflammatory, and analgesic activities [3,4,5,6]. CR contains protoberberine-type alkaloids such as berberine (BBR), palmatine (PAL), coptisine (COP), jatrorrhizine (JAT), epi-berberine (E-BBR), and columbamine (COL) [7].
We have been investigating bacterial degradation of alkaloids. Rhodococcus sp. strain BD7100 is a bacterium isolated from soil that can utilize BBR as a sole carbon source [8]. A recent report indicated that strain BD7100 degrades BBR into 2-hydroxy-3,4-dimethoxybenzeneacetic acid (HDBA) via demethylenation to D-BBR [9]. In this work, we investigated the degradation of protoberberine-type alkaloids by strain BD7100 by incubating the bacterium with CR extract, which contains numerous protoberberine-type alkaloids. Unexpectedly, we found that the number of viable cells of strain BD7100 declined, and the culture medium exhibited antimicrobial activity against strain BD7100 that increased in potency as the level of protoberberine-type alkaloids decreased. These results suggested that an antibacterial agent is produced in CR extract incubated with strain BD7100. In this study, we report a novel antimicrobial agent was being produced from the CR extract when incubated strain BD7100 in Luria–Bertani (LB) medium. We also elucidated the structure of the antimicrobial agent using NMR and MS analysis and report its total synthesis and spectrum of activity.
Results and Discussion
Production of antimicrobial agent from CR extract by Rhodococcus sp. strain BD7100 in LB medium
CR extract was added to LB medium and incubated with cells of strain BD7100. After 48 h, the culture broth was analyzed using HPLC. BBR, PAL, COP, JAT, E-BBR, and COL were detected in samples analyzed by HPLC at the beginning of the incubation period (Fig. 1a, b). HPLC chromatograms indicated that BBR, COP, and JAT were degraded during incubation, and demethyleneberberine and demethylenecoptisine were produced. BBR, COP, and JAT were completely degraded by 48 h, whereas PAL, E-BBR, and COL were still detected after 48 h (Figure S1).
Incubation of CR extract with Rhodococcus sp. strain BD7100 in LB medium. a Chemical structures of protoberberine-type alkaloids identified in CR extract. b HPLC chromatograms (λ = 280 nm) of CR extract incubated with cells of strain BD7100. c Change in the number of viable bacteria. Solid line indicates the number of viable bacteria in LB medium, and dotted line indicates the number of viable bacteria in LB medium containing CR extract. Each value represents the mean ± SD of four independent experiments
The number of viable BD7100 cells in culture broth with and without CR extract was determined using the dilution-plate method (Fig. 1c). The viable cell counts exhibited similar trends until 36 h. In culture broth containing CR extract, the number of viable cells decreased markedly by 48 h. Antibacterial activity in culture broth containing CR extract was tested against strain BD7100 using the paper-disk method. At 36 and 48 h, culture broth exhibited antibacterial activity against BD7100 cells; however, there was no activity observed at other time points (Table 1). These results suggested that one or more antimicrobial compounds active against strain BD7100 is produced in CR extract incubated with BD7100 cells. Then we tried to bioassay-guided isolation to identify bioactive compounds.
Elucidation of the structure of coptirhoquinone A (1)
Compound 1 was isolated as a red, amorphous solid, and the molecular formula was determined as C12H14O6S (six degrees of unsaturation) by high-resolution electrospray ionization mass spectrometry (HRESIMS). IR spectra (1740, 1716, and 1653 cm−1) and 13C NMR signals indicated the presence of two α, β-unsaturated ketones (δC 181.1 and 180.2) and an ester bond (δC 169.7) in the structure of 1. 1H NMR spectra of 1 exhibited signals for three methyl groups with an oxygen atom (δH 4.01, 4.00, and 3.70), a methyl group with a sulfur atom (δH 2.56), and a methylene group (δH 3.77). A heteronuclear multiple bond coherence (HMBC) correlation of 8-OCH3 [δH 3.70 (s)] with C-8 (δC 169.7) indicated the presence of a methyl ester residue. HMBC correlations of 3-OCH3 (δH 4.01 [s]) with C-3 (δC 145.4) and 4-OCH3 (δH 4.00 [s]) with C-4 (δC 144.9) indicated linkages between two methoxy groups at the C-3 and C-4 positions. An HMBC correlation of 6-SCH3 (δH 2.56 [s]) with C-6 (δC 145.6) indicated a linkage between a sulfurated methyl group and the C-6 position. From these results, the structure of 1 was determined as shown in Fig. 2 and Table 2.
Total chemical synthesis of coptirhoquinone A (1)
Total synthesis of compound 1 was carried out to confirm its structure. Benzylation of known phenol 4 [10, 11] (readily derived from 2,3,4-trimethoxylbenzaldehyde in three steps) with benzyl bromide in the presence of K2CO3 afforded benzyl ether 5 at 94% yield (Scheme 1). Rearrangement of 5 with HMBI (7) (1H-1-hydroxy-5-methyl-1,2,3-benziodoxanthiole 3,3-dioxide) [12] and trimethyl orthoformate was carried out at room temperature for 2 h to furnish the methyl acetate 6 at 66% yield [13]. Bromination of 6 with NH4Br-oxone [14] brought about the expected bromination to give the desired product 8 at 67% yield. Hydrogenation of 8 with Pd/C, followed by oxidation of the resulting phenol 9 with nBu4NBr-oxone [15], gave quinone 10 at 76% yield over two steps. Finally, substitution of 10 with sodium thiomethoxide [16] gave the desired product 1 at 76% yield. The spectroscopic data of synthesized 1 were superimposable with those of the natural product. Thus, we accomplished the total synthesis of 1 in six steps from 4 at 16.3% overall yield (Scheme 1).
Antimicrobial activity of coptirhoquinone A (1)
The antibacterial activity of 1 against strain BD7100 and various intestinal bacteria was tested using the paper-disk method (Table 3). In the presence of disks permeated with 1, growth of strain BD7100 was inhibited at 0.25 mg per disk (25.7 mm), similar to the same concentrations of ampicillin and kanamycin (25 and 24.7 mm, respectively). Compound 1 also inhibited the growth of Staphylococcus aureus (32.7 mm) and Proteus mirabillis (16.3 mm) at 0.25 mg per disk. No inhibition of the growth of Escherichia coli, Klebsiella neumoniae, or Pseudomonus aerginosa was observed.
Compound 1 was also tested for activity against pathogens associated with deep mycosis, such as Aspergillus fumigatus, A. niger, Candida albicans, and Cryptococcus neoformans. Compound 1 inhibited the growth of A. fumigatus (12.3 mm), C. albicans (10.3 mm), and C. neoformans (12.7 mm).
Compounds consisting of a benzoquinone skeleton have been reported to exhibit antibacterial activity against a variety of microorganisms [17, 18], and synthesis of various derivatives has been reported [19]. In particular, benzoquinone derivatives containing a methylthio group reportedly exhibit enhanced antibacterial activity. However, the isolation of natural benzoquinone derivatives containing methylthio groups is rare; examples include T1801B, isolated from the bacterium Pseudomonas [20], and thiographisquinone, isolated from Graphis [21], both of which consist of a 2-methylthio-3,4-benzoquinone skeleton. T1801B reportedly exhibits antibacterial activity against S. aureus and C. neoformans.
In this study, a novel antimicrobial substance was produced by incubating CR extract with a BBR-utilizing bacterium. These results suggest that it would be possible to more effectively utilize resources by preparing CR extract from waste generated during the manufacture of herbal medicine preparations and using it as a raw material. In addition, this study serves as a model for the preparation of novel compounds by the biotransformation of herbal extracts, and we hypothesize that the results could be applied to other herbal extracts and bacteria.
Materials and methods
Experimental instruments
UV and IR spectra were recorded on an Ultrospec 2100 pro UV-visible spectrophotometer (Amersham Biosciences, Ltd., Tokyo, Japan) and a FT/IR-4100 instrument (JASCO Co., Ltd., Tokyo, Japan), respectively. 1H and 13C NMR spectra were recorded using a Bruker AVANCE-400 spectrometer (400.13 MHz for 1H, 100.61 MHz for 13C; Bruker Biospin K.K., Kanagawa, Japan). Chemical shifts (δ) were measured in ppm using tetramethylsilane as an internal standard. BioShakers BR43-FH (TAITEC Co., Ltd., Saitama, Japan) and FTW-502M (Hirayama Manufacturing Corp., Saitama, Japan) were used for incubation of bacteria. The turbidity of cultures was monitored using an OD-MonitorA&S (TAITEC Co.). Samples were analyzed and quantified by PDA-HPLC using PU-980 and PU-1580 pumps (JASCO Co.) equipped with an Inertsil ODS-3 column (5 µm, 4.6 mm × 250 mm; GL Science Inc., Tokyo, Japan; maintained at a temperature of 30 °C using a CO-2065 Plus column oven [JASCO Co.]) and an MD-2010 Plus photodiode array detector (JASCO Co.). Compounds were isolated using a reverse-phase MPLC system equipped with an SSC-3160 pump (Senshu Scientific Co., Ltd., Tokyo, Japan), ULTRA PACK ODS-SM-50A column (300 mm × 11 mm [50 µm], Yamazen Corp., Osaka, Japan), and YRU-8883 RI-UV detector (Shimamuratech, Tokyo, Japan). Reverse-phase HPLC was also carried out using an LC-20AT prominence pump (Shimadzu Corp., Kyoto, Japan) equipped with an Inertsil ODS-3 column (250 mm × 4.6 mm [5 µm], GL Science Inc.), CO-965 column oven (JASCO Co.), and SPD-20A UV detector (Shimadzu Corp.). Molecular weight and molecular formula were determined by LC-ESI-TOF-MS using a JMS-T100LP spectrometer (JEOL, Ltd., Tokyo, Japan) and 1200 series system (Agilent Technologies, Inc., Tokyo, Japan).
Strains and culture conditions
The isolation and identification of Rhodococcus sp. strain BD7100 has been described previously [9]. For the present work, strain BD7100 was incubated in LB medium (0.5 g Bacto yeast extract, 1.0 g Bacto tryptone, and 0.5 g NaCl in 100 mL of water) or on 0.1 × LB agar medium (containing Bacto yeast extract and Bacto tryptone at 10-fold lower levels and 1.5% [w/v] agar). CR extract was added to these media as indicated.
Preparation of CR extract
Dried Coptidis rhizome (100 g, Uchida Wakan-yaku, Tokyo, Japan) was boiled in water (590 mL) at 100 °C for 30 min, and the extract was then filtered directly. The filtrate was centrifuged (2610 × g, r.t., 15 min), and the supernatant was filtered using a sterilized 0.2-µm filter. The resulting filtrate was used as the CR extract.
Incubation of CR extract with strain BD7100 in LB medium
Rhodococcus sp. strain BD7100 was grown at 30 °C on 0.1 × LB agar plates containing 1.0 mM BBR. Individual colonies of strain BD7100 were used to inoculate 10 mL of LB medium in a test tube, which was incubated for 24 h at 30 °C on a rotary shaker (180 rpm). After incubation, the culture was inoculated into LB medium (100 mL) containing CR extract (5 mL) in a 500-mL Erlenmeyer flask rotated at 180 rpm. Next, 0.5-mL samples of the culture were collected at various time points and mixed with an equal amount of methanol (MeOH) containing 0.4% (v/v) hydrochloric acid. This mixture was centrifuged (18,800 × g, 4 °C, 5 min) to remove cells and debris.
PDA-HPLC analysis
The flow rate was 1 mL/min, and the column oven temperature was 30 °C. Analysis was performed using a mobile phase gradient as follows. Initial conditions were 15% for 5 min, followed by a linear gradient to 50% B from 5 to 15 min and 100% B at 15.1 min, which was maintained until 18 min. The mobile phase was returned to initial conditions at 18.1 min and maintained until the end of the run at 25 min. Mobile phase solvents A and B were H2O containing 0.1% trifluoroacetic acid and acetonitrile, respectively.
Determination of the number of viable bacteria
Rhodococcus sp. strain BD7100 was incubated in flasks (500 mL) containing 100 mL of LB medium with or without 5 mL of CR extract at 30 °C with rotation (180 rpm). Samples (100 µL) of the cultures were collected at 12, 24, 36, and 48 h of incubation and diluted 107 fold using sterilized water. Aliquots (100 µL) of the diluted cultures were inoculated onto LB agar plates, which were incubated at 30 °C for 48 h. After incubation, colonies on the plates were counted.
Investigation of antibacterial activity in cultures containing CR extract
Strain BD7100 was incubated in LB medium containing CR extract. The incubation conditions were the same as those described above. After incubation, 20 mL of each culture was removed, frozen, and lyophilized. Next, 1 mL of MeOH containing 0.4% (v/v) hydrochloric acid was added to each sample and centrifuged (2610 × g, r.t., 10 min). The resulting supernatant was used to test antibacterial activity using the paper-disk method.
Testing antibacterial activity using the paper-disk method
A 50-µL aliquot of sample was applied to an 8-mm disk. The test samples were dissolved in MeOH containing 0.4% (v/v) hydrochloric acid. The disks containing sample were placed on an LB agar plate inoculated with bacteria, and the plate was incubated at 30 °C for 12 or 24 h. After incubation, the diameter of inhibitory zone around each disk was measured.
Isolation of compound coptirhoquinone A (1)
Rhodococcus sp. strain BD7100 was incubated in 36 flasks containing LB medium (100 mL) with CR extract (5 mL) at 30 °C for 48 h. The culture was then centrifuged (2610 × g, r.t., 15 min) to remove cells, and the resulting supernatant was extracted using two volumes of ethyl acetate, two volumes of ethyl acetate containing 0.08% (v/v) hydrochloric acid, and an equal volume of ethyl acetate. The ethyl acetate was evaporated, and the residue (2.08 g) was suspended in water. The suspension was extracted twice with chloroform, and then the chloroform was evaporated. The chloroform extract (571.8 mg) was dissolved in MeOH, and the solution was fractionated using a reverse-phase MPLC system at a flow rate of 5 mL/min and the following gradient: initial conditions, 0% B (0–30 min); 15% (30–75 min), 30% B (75–105 min), 50% (105–125 min), 70% B (125–160 min), 100% (160–180 min) (A: H2O, B: acetonitrile). The sixth fraction was chromatographed to isolate and purify compound 1 (3.0 mg) using reverse-phase HPLC under the following conditions: flow rate, 1.0 mL/min; column oven temperature, 30 °C; detector, UV at 210 nm; mobile phase, 65% H2O containing 0.1% (v/v) trifluoroacetic acid and 35% acetonitrile.
Compound 1: Red, amorphous solid; HRESIMS obsd. 287.0601 calcd. for C12H15O6S1 [M+H]+ 287.0589; UV λmax (MeOH) nm (log ε): 206 (4.0), 270 (3.5), 342 (3.4); IR (KBr) cm−1: 1740, 1716, 1653. The NMR data see Table 2.
General methods
Melting points were determined using a Yanagimoto MP apparatus, and the values are uncorrected. Optical rotations were measured using a JASCO DIP-360. IR spectra were obtained using a JASCO FT/IR-4100 spectrophotometer. 1H and 13C NMR spectra were obtained on a Bruker AV III 400 (1H-NMR: 400 MHz, 13C NMR: 100 MHz) instrument for solutions in CDCl3, and chemical shifts are reported on the δ scale using TMS as an internal standard of 0.00 for 1H NMR spectra and CDCl3 as an internal standard of δ 77.00 for 13C NMR spectra. MS spectra were obtained on a JEOL-600 spectrometer. Elemental analyses were performed on a Yanaco-MT5.
2,3,4-Trimethoxyphenol
To a solution of 2,3,4-trimethoxybenzaldehyde (1.0 g, 5.1 mmol) in MeOH (7.3 mL), 31% H2O2 (0.75 mg, 6.6 mmol) and H2SO4 (0.07 mL) were added at room temperature. After stirring for 12 h at the same temperature, the volatile solvent was removed in vacuo to leave a residue. The residue was treated with H2O (30 mL) and extracted twice with CHCl3. The extract was washed with H2O, saturated NaHCO3 aqueous solution, and brine. The organic layer was dried over Na2SO4 and concentrated in vacuo to give crude 2,3,4-trimethoxyphenol (1.1 g), which was used for the next step without further purification.
1H NMR (CDCl3; 400 MHz) δ 6.63 (1H, d, J = 9.0 Hz), 6.56 (1H, d, J = 9.0 Hz), 5.39 (1H, s), 3.96 (3H, s), 3.90 (3H, s), 3.81 (3H, s).
2,3,4-Trimethoxyphenyl acetate
To the crude 2,3,4-trimethoxyphenol (1.1 g) and pyridine (2.0 g, 25.5 mmol) in CHCl3 (20 mL), Ac2O (1.9 mL, 20.4 mmol) and pyridine (12 mL, 95.4 mmol) were added at room temperature under Ar gas. After stirring for 6 h at the same temperature, the reaction mixture was treated with H2O and extracted with ethyl acetate (EtOAc). The extract was washed with saturated KHSO4 aqueous solution, brine, saturated NaHCO3 aqueous solution, and brine. The organic layer was dried over Na2SO4 and concentrated in vacuo to give 2,3,4-trimethoxyphenylacetate (1.2 g), which was used for the next step without further purification. 1H NMR (CDCl3; 400 MHz) δ 6.71 (1H, d, J = 9.0 Hz), 6.59 (1H, d, J = 9.0 Hz), 3.86 (3H, s), 3.85 (3H, s), 3.82 (3H, s), 2.28 (3H, s).
1-(2-Hydroxy-3,4,5-trimethoxyphenyl)ethanone (4)
To the crude 2,3,4-trimethoxyphenylacetate (1.2 g), BF3·OEt2 (4 mL, 31.8 mmol) was added at room temperature under Ar gas. After stirring for 30 min at 100 °C, the reaction mixture was poured into H2O, and the resulting mixture was extracted with EtOAc. The organic layer was washed with saturated NaHCO3 aqueous solution, brine, and then dried over Na2SO4. Removal of the solvent gave a residue, which was purified by column chromatography using hexane-EtOAc (8:2, v/v) as the eluent to give 1-(2-hydroxy-3,4,5-trimethoxyphenyl)ethanone (4) (690.1 mg, 68%) as a yellow solid. 1H-NMR (CDCl3; 400 MHz) δ 12.44 (1H, s), 6.93 (1H, s), 4.04 (3H, s), 3.92 (3H, s), 3.86 (3H, s), 2.59 (3H, s); 13C-NMR (CDCl3; 100 MHz) δ 203.1, 153.1, 149.9, 145.0, 141.4, 114.2, 107.4, 61.3, 61.0, 59.7, 26.7.
1-(2-[Benzyloxy]-3,4,5-trimethoxyphenyl)ethanone (5)
To a solution of 1-(2-hydroxy-3,4,5-trimethoxyphenyl)ethanone (4) (94.6 mg, 0.42 mmol) in acetone, K2CO3 (122.0 mg, 0.88 mmol) and BnBr (74.6 μL, 0.63 mmol) were added at room temperature under Ar gas. After stirring for 49.5 h at the same temperature, the reaction mixture was diluted with EtOAc and then filtered through a pad of Celite. The filtrate was removed in vacuo. The residue was purified by column chromatography on silica gel using hexane-EtOAc (8:2, v/v) as the eluent to give benzyl ether 5 (124.9 mg, 94%) as a yellowish oil. IR ν max 1672, 1117, 1065 cm−1; 1H NMR (CDCl3; 400 MHz) δ 7.45–7.33 (5H, m), 5.06 (1H, s), 3.99 (3H, s), 3.94 (3H, s), 3.87 (3H, s), 2.56 (3H, s); 13C NMR (CDCl3; 100 MHz) δ 198.5, 149.3, 147.1, 147.1, 147.0, 136.8, 128.6, 128.3, 128.3, 127.5, 106.5, 76.4, 61.4, 61.2, 56.1, 31.4; HRMS (ESI+) calcd for C18H21O5 [M+H]: 317.1389; found: 317.1392.
Methyl 2-(2-[benzyloxy]-3,4,5-trimethoxyphenyl)acetate (6)
To a solution of the benzyl ether 5 (54.1 mg, 0.17 mmol) in MeOH (2 mL), H2SO4 (8.4 mg, 0.09 mmol) and trimethyl orthoformate (0.6 mL) were added at room temperature. After stirring for 10 min at the same temperature, HMBI (7, 1H-1-hydroxy-5-methyl-1,2,3-benziodoxanthiole 3,3-dioxide) (54 mg, 0.17 mmol) was added to the reaction mixture. After stirring for 15 min, HMBI (60 mg, 0.19 mmol) was added to the above mixture. After stirring for 2 h, the reaction mixture was poured into H2O, and the resulting mixture was extracted with EtOAc. The extract was washed with saturated NaHCO3 aqueous solution, brine, and dried over Na2SO4. Removal of the solvent gave a residue, which was purified by column chromatography on silica gel using hexane-EtOAc (8:2, v/v) as the eluent to give phenylacetate 6 (38.8 mg, 66%) as a yellowish oil. IR ν max 1739, 1494, 1464, 1128, 1087 cm−1; 1H NMR (CDCl3; 400 MHz) δ 7.49–7.30 (5H, m), 6.52 (1H, s), 4.99 (2H, s), 3.94 (3H, s), 3.91 (3H, s), 3.83 (3H, s), 3.64 (3H, s), 3.56 (2H, s); 13C NMR (CDCl3; 100 MHz) δ 172.2, 149.4, 147.1, 144.3, 142.3, 137.6, 128.3, 128.1, 127.9, 122.4, 108.2, 75.1, 61.1, 56.1, 51.9, 35.4; HRMS (ESI+) calcd for C19H22NaO6 [M+Na]: 369.1314; found: 369.1322.
Methyl 2-(2-[benzyloxy]-6-bromo-3,4,5-trimethoxyphenyl)acetate (8)
To a solution of methyl phenylacetate 6 (77.4 mg, 0.33 mmol) in MeOH-H2O (1:1, 6 mL), NH4Br (33.9 mg, 0.35 mmol) and oxone (151.3 mg, 0.25 mmol) were added at 0 °C. After stirring for 30 min at the same temperature, the reaction was quenched with H2O, and the whole sample was extracted with EtOAc. The extract was washed with saturated Na2S2O3 aqueous solution, saturated NaHCO3 aqueous solution, and brine, and then dried over Na2SO4. The solvent was removed in vacuo to leave a residue, which was purified by column chromatography on silica gel using hexane-EtOAc (85:15, v/v) as the eluent to give bromobenzene 8 (64.1 mg, 67%) as a colorless oil. IR ν max 1743, 1415, 1083, 1042 cm−1; 1H NMR (CDCl3; 400 MHz) δ 7.43–7.32 (5H, m), 5.00 (2H, s), 3.97 (3H, s), 3.93 (3H, s), 3.87 (3H, s), 3.82 (2H, s), 3.66 (3H, s); 13C NMR (CDCl3; 100 MHz) δ 171.3, 147.8, 147.4, 147.1, 146.5, 137.2, 128.5, 128.1, 128.1, 124.2, 114.8, 75.6, 61.4, 61.2, 61.0, 52.0, 35.7; HRMS (ESI+) calcd for C19H2179BrNaO6 [M+Na]: 447.0419; found: 447.0406.
Methyl 2-(2-bromo-6-hydroxy-3,4,5-trimethoxyphenyl)acetate (9)
To a solution of bromobenzene 8 (52.5 mg, 0.12 mmol) in MeOH (4 mL), 10% Pd/C (4.2 mg) was added under an atmosphere of H2 at room temperature. After stirring for 1.5 h at the same temperature, the reaction mixture was filtered through a pad of celite. The filtrate was concentrated to leave a residue, which was used for the next steps without further purification.
Methyl 2-(2-bromo-4,5-dimethoxy-3,6-dioxocyclohexa-1,4-dienyl)acetate (10)
To a solution of the corresponding phenol 9 (45.4 mg) in CH3CN-H2O (2:1, 6 mL), nBu4NBr (4.7 mg, 0.01 mmol) and oxone (64.7 mg, 0.11 mmol) were added at 0 °C. After stirring for 2.5 h at the same temperature, the reaction mixture was filtered through a pad of SiO2. The filtrate was concentrated in vacuo to leave a residue, which was purified by column chromatography on silica gel using hexane-EtOAc (30%, v/v) as the eluent to give quinone 10 (30.1 mg, 76%) as a reddish oil. IR ν max 1743, 1669, 1604, 1262 cm−1; 1H NMR (CDCl3; 400 MHz) δ 4.05 (3H, s), 4.03 (3H, s), 3.76 (2H, s), 3.73 (3H, s); 13C NMR (CDCl3; 100 MHz) δ 180.1, 176.3, 168.4, 145.1, 144.3, 139.9, 136.0, 61.6, 61.3, 52.5, 35.8; HRMS (ESI+) calcd for C11H1279BrO6 [M+H]: 318.9817; found: 318.9808.
Coptirhoquinone A (1)
To a solution of quinone 10 (20.6 mg, 0.06 mmol) in CHCl3-H2O (6:1, 3.5 mL), nBu4NBr (3 mg, 9.3 μmol) and NaSMe (16.9 mg, 0.24 mmol) were added at room temperature. After stirring for 20 min at the same temperature, the reaction mixture was filtered through a pad of SiO2. The filtrate was concentrated in vacuo to leave a residue, which was purified by column chromatography using hexane-EtOAc (4:1, v/v) as the eluent to give thioquinone 1 (14.1 mg, 76%) as a reddish oil. 1H NMR (CDCl3; 400 MHz) δ 4.02 (3H, s), 4.01 (3H, s), 3.78 (2H, s), 3.71 (3H, s), 2.57 (3H, s); 13C NMR (CDCl3; 100 MHz) δ 180.9, 180.0, 169.5, 145.4, 145.2, 144.7, 137.7, 61.3, 61.2, 52.3, 33.5, 17.7.
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This work was supported by Hoshi University Otani Research Grants and a JSPS Grant-in-Aid for Young Scientists (B) (grant number 972018).
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Ishikawa, K., Takahashi, K., Hosoi, S. et al. Antimicrobial agent isolated from Coptidis rhizome extract incubated with Rhodococcus sp. strain BD7100. J Antibiot 72, 71–78 (2019). https://doi.org/10.1038/s41429-018-0114-3
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DOI: https://doi.org/10.1038/s41429-018-0114-3