Patent Application
20230314395
The present invention relates to new thiourea-based compounds, to a process for obtaining them and to their use in the detection of γ-hydroxybutyric acid (GHB) in beverages.
γ-hydroxy butyric acid (GHB) is one of the drugs used in chemical submission. It is an odorless, colorless, slightly salty compound sometimes used for recreational purposes. However, this compound, when supplied without knowledge of the victim, has been used on numerous occasions in order to commit an offense. In many of them, it is used to void the will of the victims and carry out sexual assault. In general, the intake of the drug by the victim occurs through a beverage that has been contaminated with the product without noticing the product. Residence time in the body is 3-6 hours and its metabolites are excreted rapidly, so that it is very difficult to detect their presence in the body after the assault.
Four references addressing this subject have been found in the scientific literature (J. Forensic. Sci. 2004, 49, p. 379-387, Chem. Commun. 2013, 49, p. 6170-6172, Chem. Commun. 2014, 50, p. 2904-2906, J. Mat. Chem. B 2017, 8, p. 2736-2742).
The first case (J. Forensic. Sci. 2004, 49, p. 379-387) relates to an enzymatic reaction while the other three reviews are referring to chemical sensors.
Chem. Commun. 2014, 50, 2904-2906 describes the use of Compound A as chemosensor for detecting GHB. The interaction with the analyte was based on a hydrogen bonding interaction between the phenol group on the sensor and the carboxylate unit on GHB.
In addition, the same authors also described in Chem. Commun. 2013, 49, 6170-6172 the use of Compound B for detecting the corresponding lactone (GBL), but again, the interaction was related to the formation of a hydrogen bond. However, in any case, soft drinks alone or mixed with alcoholic beverages were not tested as interferents.
On the other hand, J. Mat. Chem. B 2017, 8, 2736-2742 describes the preparation of a complex of Ir (C) capable of detecting GHB. The complex showed luminescence quenching in the presence of analyte that was observed using UV light.
By following a different approach, Bravo D. T.: Harris, D. O., Parsons S. M. J. Forensic. Sci. 2004. 49, p. 379-387 described the use of γ-hydroxybutyrate dehydrogenase (GHB-DH) to detect GHB. Enzymatic oxidation of GHB by NAD+ is combined with reduction of a dye showing a colour change. Ethanol is an interferent that can be avoided by drying the sample to be studied.
The present inventors have been able to develop a reliable and easy-to-use procedure and device that enables visual determination of whether a beverage, whether alcoholic, non-alcoholic, or combined, has been contaminated with GHB prior to ingestion. Additionally, the ready-to-use device only needs a drop of the beverage under analysis so that in case the response is negative, it can be ingested substantially entirely without any problems.
In a first aspect, the present invention relates to a compound 1 or 2 according to claim 1.
In a second aspect, the present invention also relates to a composition comprising a compound 1 or 2 according to the first aspect.
In a third aspect, the present invention also relates to a process for obtaining a compound 1 or 2 according to the first aspect.
In a fourth aspect, the present invention relates to the use of a compound 1 or 2 according to the first aspect or a composition according to the second aspect for the detection of GHB in beverages.
In a fifth aspect, the present invention relates to a procedure for detecting GHB in beverages.
In a sixth aspect, the present invention relates to equipment or kit for use in detecting GHB in beverages.
In a first aspect, the present invention relates to a compound of formula 1 or 2:
In a second aspect, the present invention relates to a composition comprising Compound 1 or 2 as defined above. In a preferred embodiment, said composition comprises Compound 1 or 2 as defined above and an organic solvent. As the organic solvent, but not limited thereto, DMF (dimethylformamide) and DMSO (dimethylsulfoxide) may be used, although DMSO is preferably utilized.
In a third aspect, the present invention relates to a process for obtaining compound 1 or 2, comprising the following reaction scheme:
The reaction conditions are not particularly relevant, as it may be carried out at room P and T.
In a fourth aspect, the present invention relates to the use of a composition, as defined above, or a compound 1 or 2, as defined above, in the detection of γ-hydroxybutyric acid (GHB) or a salt thereof in beverages. Such salts may include, but are not limited to, salts with alkali or alkaline earth metals, preferably sodium. In the present invention, when reference is made to beverages, as indicated below, it will be understood as alcoholic beverages, non-alcoholic beverages or mixtures thereof. Where reference is made to alcoholic beverages, alcoholic distillates such as, for example, whisky or gin, as well as alcoholic beverages that are not distilled, such as wine and beer, are included.
In a fifth aspect, the present invention relates to a process for detecting GHB or a salt thereof in beverages, comprising:
It should be noted that in step b) the composition of Compound 1 or 2 and the organic solvent may already be prepared or may be prepared at that point of time just before the addition of the aliquot of the solution obtained in step a).
In a preferred embodiment, said weak base in step a) is sodium bicarbonate, although any weak base such as, for example, potassium, ammonium, calcium bicarbonate could be used. In another preferred embodiment, the concentration of the aqueous solution of weak base is from 0.4 mM to 1 mM, even more preferably 0.4 mM.
In another preferred embodiment, Compound 1 or 2 is at a concentration between 50 μM and 100 μM, even more preferably 50 μM.
In step c) it should be observed if a reaction occurs between compounds 1 or 2, alone or in the composition, with the possible GHB component or a salt thereof present in the beverage to be analyzed. Whether compound 1 and compound 2 react positively with GHB or a salt thereof, a color change (from pale yellow to orange) will be observed.
Thus, one can conclude in step d) about the presence or not of GHB in the beverage being analyzed.
In another alternative embodiment of the process, this may be slightly modified in the order of mixing, although the final result would be the same. In this regard, the alternative process comprises the steps of:
In another alternative embodiment of the process, the visual detection is performed on a strip of a non-woven fabric (NWF) with 50 to 100% polypropylene, preferably with 100% polypropylene. In this case, the process for detecting GHB or a salt thereof in beverages comprises the steps of:
Compound 1 or 2 is preferably at a concentration of 50 μM to 500 μM, preferably 50 μM to 100 μM.
The reaction is considered positive in GHB if in step c) a light yellow to intense orange change is observed with compounds 1 or 2.
This detection process with a fabric strip detects GHB in all types of pure beverages (alcoholic and non-alcoholic) and combined alcoholic and non-alcoholic beverages provided that it is at a concentration above 35 μM.
In a sixth aspect, the present invention relates to a kit or equipment for use in detecting GHB or a salt thereof in beverages comprising:
In another embodiment, in the case of detecting GHB or a salt thereof in beverages by means of a strip of a non-woven fabric (NWF) with 50 to 100% polypropylene, the kit or equipment alternatively comprises:
Optionally, such a kit or equipment according to any of the preceding embodiments (whether based on strips for detection or not) further comprises instructions for use.
As noted above herein, the weak base used for the beverage sample in the kit without strip detection is preferably sodium bicarbonate, although any weak base such as potassium bicarbonate, ammonium bicarbonate, calcium bicarbonate could be used. In another preferred embodiment, the concentration of the aqueous solution of weak base is 0.4-1 mM, even more preferably 0.4 mM.
Additionally, as noted herein above, in the case of beverage detection for any of the embodiments of the kit (whether based on strips for detection or not), Compound 1 or 2 is preferably present in the composition at a concentration between 50 μM and 500 μM, preferably from 50 μM to 150 μM, more preferably from 50 μM to 100 μM.
In a preferred embodiment, such transparent containers with opening and closure, according to any of the embodiments of the kit (whether based on strips for detection or not), are microtubes, graduated or not graduated, of polypropylene (e.g., Eppendorfrm).
In another preferred embodiment of the non-strip based kit, said tool for collecting the sample can be a dropper or a small spoon. In the case of the strip-based kit, said tool is not necessary.
In a more preferred embodiment, in the use, process, or kit or equipment, as defined in the foregoing aspects, the beverage is an alcoholic beverage. In another more preferred embodiment, said alcoholic beverage is admixed with a non-alcoholic beverage, preferably a soft drink or juice. In another more preferred embodiment, said beverage is only a non-alcoholic beverage, preferably a soft drink or a juice.
Preferably, said alcoholic beverage is selected from, byway of non-limiting example, gin, vodka, rum, whisky, white wine, vermouth, and beer.
Preferably, said soft drink or juice is selected from, by way of non-limiting example, tonic, orange soft drink, lemon soft drink, cola drink, tea drink and any fruit juice.
It should be noted that any combination of previous embodiments or instances or examples encompassed by the present invention is understood by one skilled in the art as being feasible in the context of the present invention.
The various particular instances or examples recited above, as well as the following examples, are provided for illustrative purposes only and are not intended to limit the scope of the present invention in any way.
In 50 mL of MeOH, 500 mg of 3 (3.30 mmol) and 842 mg of Na2CO3 (7.91 mmol) were stirred for 30 min and then 910 μL of Boc2O (3.96 mmol) was added dropwise. Stirring was continued at room temperature until the next day. The MeOH was then removed under vacuum and about 30 mL of deionized water was added. It was extracted with AcOEt (3×20 mL), the organic layer was dried over anhydrous MgSO4, filtered and the solvent removed under vacuum. 635 mg of compound 4 was obtained in 89% yield.
365 mg of 4-(trifluoroacetyl)benzoic acid (1.67 mmol), 202 mg (1.67 mmol) of DMAP and 300 μL (1.67 mmol) of EDC were mixed in 10 mL of dry THF under inert atmosphere for 30 min. 300 mg of 4 (1.39 mmol, 0.139 M) was then dissolved in 10 mL of dry THF and added dropwise. The reaction was kept for 2 days at room temperature and under argon atmosphere. The solvent was then removed under vacuum, the resulting yellow oil was dissolved in 20 mL of AcOEt and the organic layer was washed with 1% HCl (2×10 mL), NaHCO3 (sat) (2×10 mL) and NaCl (sat) (10 mL). The organic layer was dried with anhydrous MgSO4, filtered, and the solvent removed under vacuum. 524 mg of compound 5 (91% yield) was isolated.
In 5 mL of dry DCM, 201 mg of 5 (0.48 mmol) was dissolved with 1 mL of TFA (13.06 mmol) under inert atmosphere. The mixture was stirred for 15 min and the solvent removed under vacuum. The colorless oil was dissolved in 15 mL of AcOEt and the organic layer was washed with Na2CO3 (sat) (2×10 mL) and NaCl (sat) (10 mL), dried over anhydrous MgSO4 and filtered. After evaporating the solvent, the compound 6 as a white powder (121 mg, 80% yield) was obtained.
52 mg of 4-nitrophenyl isothiocyanate (0.29 mmol) was mixed with 110 mg of 6 (0.35 mmol) in 5 mL of pyridine under inert atmosphere for 2 days. The solvent was then removed and the resulting yellow oil was dissolved in 15 mL of AcOEt. The organic layer was washed with 1 M HCl (10 mL), NaHCO3 (sat) (10 mL) and NaCl (sat) (10 mL), dried over anhydrous MgSO4 and filtered. The solvent was removed under vacuum and the reaction crude was purified by chromatographic column using Hexane:AcOEt. AcOEt as eluent (from 7:3 to 6:4). 68 mg of compound 1 was obtained (47% yield).
In 10 mL of MeOH, 500 μL of 7 (8.31 mmol) and 1400 μL of Net3 (9.97 mmol) were mixed and then 2300 μL of Boc2O (9.97 mmol) was added dropwise. Stirring was kept at room temperature for 16 h. The MeOH was then removed under vacuum and the colorless oil dissolved in 30 mL of AcOEt. The organic layer was washed with deionized water (2×15 mL) and NaCl (sat) (15 mL), dried over anhydrous MgSO4, filtered, and the solvent was removed under vacuum. 676 mg of compound 8 (50% yield) was obtained.
807 mg of 4-(trifluoroacetyl)benzoic acid (3.70 mmol), 452 mg of DMAP (3.70 mmol) and 660 μL of EDC (3.70 mmol) were dissolved in 10 mL of dry THF under inert atmosphere. After 45 min stirring, 500 mg of 8 was dissolved in 10 mL of dry THF and added thereto. Stirring was kept at room temperature for 2 days. The solvent was then removed under vacuum and the resulting yellow oil was dissolved in 30 mL AcOEt. The organic layer was washed with 1% HCl (15 mL), NaHCO3 (sat) (2×15 mL) and NaCl (sat) (15 mL), dried over anhydrous MgSO4 and filtered. 1 g of compound 9 was obtained in 90% yield.
In 4.5 mL of dry DCM, 1 g of 9 (2.77 mmol) and 1 mL of TFA (13.06 mmol) were mixed for 15 min under inert atmosphere. The solvent was then removed and compound 10 was isolated (616 mg, 60% yield).
566 mg of 10 (2.17 mmol, 0.109 M) and 323 mg of 4-nitrophenyl isothiocyanate (1.81 mmol) were dissolved in 20 mL of pyridine under inert atmosphere. Stirring was kept at room temperature for 2 days. The solvent was then removed under vacuum and the resulting yellow oil dissolved in 30 mL of AcOEt. The organic layer was washed with 1 M HCl (15 mL), NaHCO3 (sat) (2×15 mL) and NaCl (sat) (15 mL), dried over anhydrous MgSO4, filtered and the solvent removed under vacuum. The crude reaction was purified by chromatography column using Hexane:AcOEt (from 7:3 to 6:4) as eluent. 400 g of compound 2 was isolated in 50% yield.
Firstly, the beverages were contaminated with GHB at a concentration of 24 mM. An aliquot of 100 μL was then taken and mixed with 100 μL of NaHCO3 (1 mM or 0.4 mM). 30 μL of this solution were then taken and mixed with 50 μL of a solution of Compound 1 or 2 (1 mM in DMSO) and 920 μL of DMSO. The same process was followed for samples without GHB.
Results are seen in
A strip of a 100% polypropylene non-woven fabric (NWF) of 0.5×3.0 cm was introduced into the beverage for three seconds and then brought to a vial containing a 125 μM concentration sensor solution in DMSO. Upon contact of the strip with the sensor, the color change from light yellow to intense orange occurred for both compounds 1 and 2 The system detects all types of combinations provided that the concentration is above 35 μM.
| Number | Date | Country | Kind |
|---|---|---|---|
| P202030841 | Aug 2020 | ES | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/ES2021/070596 | 8/5/2021 | WO |
