Patent Application
20230373881
The present invention relates to a method for producing astatine-211, and a method for producing an astatine-211-labeled compound using the astatine-211 produced by this method.
Astatine is one of the halogen elements and considered to have chemical properties similar to those of iodine. Astatine has multiple isotopes but no stable isotopes, all of which are radioactive isotopes. Astatine-211 is one of the radioactive isotopes and has recently attracted attention since it can be used for RI internal therapy that selectively destroys cancer cells.
As a production method of astatine-211, a wet separation method and a dry separation method are known. Since the wet separation method has problems such as contamination with impurities, the dry separation method is currently the mainstream. In the dry separation method, 1) a step of generating astatine-211 by irradiating bismuth with α rays, 2) a step of heating the generated astatine-211 to vaporize, 3) a step of cooling the astatine-211 that has been vaporized to collect the astatine-211 with a solvent, and 4) a step of removing the solvent are sequentially performed, to produce astatine-211. Although it has long been pointed out that astatine scatters together with the solvent when removing the solvent since astatine is easily volatile, scattering of astatine-211 can be prevented by using chloroform as a solvent (Non Patent Literature 1).
[Non Patent Literature 1] E. Aneheim et al., Sci Rep. 2019 Nov. 4; 9 (1): 15900
As described above, use of chloroform as a solvent can prevent scattering of astatine-211 and allow collection of astatine-211 with high recovery. However, when chloroform is used as a solvent, astatine-211 is contaminated, albeit in very small amounts, with chloride ions liberated from chloroform. Such contamination with chloride ions does not matter much when the labeling reaction with astatine-211 is an electrophilic substitution reaction. However, when the labeling reaction is a nucleophilic substitution reaction, the chloride ions react with a labeling precursor instead of astatine-211, which is a big problem.
The present invention has accomplished under such a situation, and it is an object of the present invention to provide a method for preventing astatine-211 from scattering without using chloroform when removing a solvent from an astatine-211 solution.
As a result of diligent studies in order to solve the above problem, the present inventors have found that scattering of astatine-211 can be prevented without using chloroform by collecting astatine-211 with a chlorine-free solvent such as alcohol, adding a carbonate or bicarbonate to the astatine solution obtained, and then removing the solvent, thereby having accomplished the present invention.
That is, the present invention provides [1] to [12] below.
[5] The method for producing astatine-211 according to any of [1] to [4], wherein the volatile and polar solvent is methanol, ethanol, 2-propanol, or acetonitrile.
The method for producing an astatine-211-labeled compound according to [9] or [10], wherein the labeling precursor compound is a compound having a trimethylsilyl group or a tributylstannyl group, and the astatine-211-labeled compound is a compound in which the trimethylsilyl group or the tributylstannyl group in the labeling precursor compound is substituted with astatine-211.
The present specification includes the contents described in the specification and/or drawings of Japanese Patent Application No. 2020-081819, which is the basis of the priority of the present application.
The present invention provides a novel method for producing astatine-211. According to the production method of the present invention, astatine-211 without contamination of chloride ions can be produced in high yield.
Hereinafter, the present invention will be described in detail.
The method for producing astatine-211 of the present invention comprises the following steps (1) to (5).
In step (1), bismuth is irradiated with α rays to generate astatine-211.
Bismuth can be irradiated with α rays using an accelerator. Irradiation with α rays causes a nuclear reaction of 209Bi(α,2n)211At to generate astatine-211.
In step (2), the astatine-211 generated in step (1) is heated to vaporize.
The astatine-211 is heated in a furnace. The temperature in the furnace is not specifically limited, as long as it is a temperature at which the astatine-211 can be vaporized, but is preferably 600 to 900° C., more preferably 800 to 900° C.
In step (3), the astatine-211 that has been vaporized in step (2) is cooled and collected with a volatile and polar solvent to obtain an astatine-211 solution.
The method for cooling the astatine-211 is not specifically limited, and examples thereof can include a method of feeding the astatine-211 that has been vaporized in a furnace into a tube (cooling trap) set in a tank filled with a low-temperature liquid using a carrier gas. The carrier gas may be those generally used in a dry separation method of astatine-211 such as helium or a mixed gas of nitrogen and oxygen. The liquid used for the cooling trap also may be those generally used in a dry separation method of astatine-211, and examples thereof may include liquid nitrogen and ethanol with dry ice.
The method for collecting astatine-211 with a solvent is not specifically limited, and in the case of cooling the astatine-211 using a cooling trap, as described above, examples thereof can include a method of passing the solvent through the tube of the cooling trap.
The solvent to be used is not specifically limited, as long as it is volatile and polar. For example, methanol, ethanol, 2-propanol, or acetonitrile can be used. Among these, methanol is preferable since it has a low boiling point and is easily volatile.
The solvent is preferably free from water. This is because the labeling reaction of astatine-211 may be performed under anhydrous conditions (for example, the labeling reaction of astatine-211 of formula (I)-1 or formula (I)-2 described below is performed under anhydrous conditions), and water is difficult to volatilize and may remain to adversely affect the reaction.
Further, the solvent is preferably free from halogen atoms in its molecule. This is because, in the case of using a solvent containing a halogen atom in its molecule, halide ions liberated from the solvent may adversely affect the reaction between astatine-211 and a labeling precursor compound.
In step (4), a weak acid salt is added to the astatine-211 solution obtained in step (3) to obtain an astatine-211 solution containing the weak acid salt.
As a weak acid salt, a carbonate, a bicarbonate, a phosphate, a hydrogen phosphate, a dihydrogen phosphate, an acetate, or the like can be used. Among these, a carbonate or bicarbonate is preferably used. This is because carbonate ions and bicarbonate ions contained in the carbonate and bicarbonate vaporize as CO2 and H2O, and thus can be easily removed. The carbonate and bicarbonate are preferably salts of alkali metals, and preferred examples thereof include NaHCO3, Na2CO3, KHCO3, K2CO3, CsHCO3, and Cs2CO3.
The concentration of the weak acid salt in the astatine-211 solution is not specifically limited, as long as it can prevent scattering of astatine-211, but is preferably 0.2 to 2.0 M, more preferably 0.3 to 1.5 M, even more preferably 0.5 to 1.0 M.
In step (5), the solvent is removed from the astatine-211 solution containing the weak acid salt obtained in step (4).
The method for removing the solvent is preferably a method in which astatine-211 is difficult to scatter, and examples thereof can include a method for removing a solvent by spraying a nitrogen gas.
The first production method of an astatine-211-labeled compound of the present invention is a method for producing an astatine-211-labeled compound comprising reacting the astatine-211 produced by the method above for producing astatine-211 of the present invention (which will be hereinafter referred to as “the astatine-211 of the present invention”) with a labeling precursor compound to produce an astatine-211-labeled compound, wherein the reaction is a nucleophilic substitution reaction.
The astatine-211 collected with a solvent such as alcohol is presumed to be present in the anionic state (211At−) in the astatine-211 solution. Accordingly, the astatine-211 of the present invention acts as a nucleophilic reagent in a nucleophilic substitution reaction and reacts with various labeling precursor compounds to generate an astatine-211-labeled compound.
The labeling precursor compound to be used is not specifically limited, but a compound having a leaving group for a nucleophilic substitution reaction of astatine-211 is preferable. The leaving group is not specifically limited, and examples thereof include alkylsulfonyloxy groups such as a methanesulfonyloxy group, haloalkylsulfonyloxy groups such as a trifluoromethanesulfonyloxy group, or arylsulfonyloxy groups such as a p-toluenesulfonyloxy group. Suitable examples of the leaving group can include a trifluoromethanesulfonyloxy group or a p-toluenesulfonyloxy group. Further, a compound that stabilizes astatine-211 in vivo has been reported recently (WO2019/151384). The labeling precursor compound to be used in the present invention may be those that generate such a compound by reaction with astatine-211. For example, a compound represented by formula (I)-1 or formula (I)-2 below generates an astatine-211-containing compound (compound represented by formula (II) described below) that is stable in vivo by reaction with astatine-211, and such a compound may be used as a labeling precursor compound.
In the case of using a compound having a p-toluenesulfonyloxy group or trifluoromethanesulfonyloxy group as a labeling precursor compound, the astatine-211-labeled compound to be generated is a compound in which the p-toluenesulfonyloxy group or trifluoromethanesulfonyloxy group in the labeling precursor compound is substituted with astatine-211. Further, in the case of using the compound represented by formula (I)-1 or formula (I)-2 above as a labeling precursor compound, the astatine-211-labeled compound to be generated is a compound represented by formula (II) below.
The temperature, the time, and the solvent to be used in the reaction of the astatine-211 of the present invention with the labeling precursor compound can be determined according to each reaction. For example, in the case of a reaction of the astatine-211 of the present invention with the compound represented by formula (I)-1, the reaction temperature can be 50 to 150° C., preferably 80 to 120° C., the reaction time can be 10 to 60 minutes, preferably 20 to 40 minutes, and acetonitrile can be used as a solvent. Further, in the case of a reaction of the astatine-211 of the present invention with the compound represented by formula (I)-2, the reaction temperature can be 10 to 30° C., preferably 15 to 25° C., the reaction time can be 10 to 60 minutes, preferably 20 to 40 minutes, and acetonitrile can be used as a solvent.
The second production method of the astatine-211-labeled compound of the present invention is a method for producing an astatine-211-labeled compound comprising reacting the astatine-211 of the present invention with a labeling precursor compound to produce an astatine-211-labeled compound, wherein the reaction is an electrophilic substitution reaction.
The electrophilic substitution reaction is not specifically limited but is preferably an aromatic electrophilic substitution reaction in which a leaving group on an aromatic ring is substituted with astatine-211.
The labeling precursor compound to be used is not specifically limited, but a compound having a leaving group that can be easily substituted with astatine-211, such as a trialkylsilyl group and a trialkylstannyl group, is preferable. Examples of the trialkylsilyl group can include a trimethylsilyl group, a triethylsilyl group, a tri n-propylsilyl group, a triisopropylsilyl group, and a tri n-butylsilyl group. Among these, a trimethylsilyl group (—SiMe3) is preferable. Examples of the trialkylstannyl group can include a trimethylstannyl group, a triethylstannyl group, a tripropylstannyl group, and a tributylstannyl group. Among these, a tributylstannyl group (—SnBu3) is preferable. In addition, since astatine-211-metaastatobenzylguanidine has recently attracted attention as an α-ray cancer therapeutic agent, metatrimethylsilylbenzylguanidine that is the precursor of this compound may be used as a labeling precursor compound.
Hereinafter, the present invention will be described further in detail by way of examples, but the present invention is not limited to these examples.
Astatine-211 (211At) was produced by irradiating a stable isotope of bismuth with an α beam using a cyclotron to cause a nuclear reaction of 209Bi (α,2n)211At. The 211At was isolated from bismuth after irradiation (using a mixed gas of nitrogen and oxygen as a carrier gas) by heating in a furnace at 850° C. for distillation and was collected by washing a trap tube on the downstream in any solvent. The 211At solution thus obtained was concentrated by the following method.
100 μL of the 211At solution collected with methanol was added to a vial into which 72.4 μmol of a bicarbonate salt and a carbonate salt of sodium, potassium, cesium, and the like was put in advance, and the resulting mixture was mixed well. The 211At solution was mixed with the bicarbonate or carbonate within 60 minutes after collection. Thereafter, a vent needle connected to activated carbon was attached thereto, and the solvent was removed with a nitrogen gas. The radioactivity of 211At in the vial before and after the solvent was removed was measured, to determine the 211At residual rate (Table 1).
211At residual rate
As shown in Table 1, the 211At residual rate significantly increased when any salt was added, as compared with the case where no salt was added.
After removing the solvent from the 211At solution, a labeling precursor (I)-1 or (I)-2 (21.3 μmol/300 μL) dissolved in anhydrous acetonitrile was added and mixed using a vortex mixer. The labeling precursor (I)-1 was reacted at 100° C., and the labeling precursor (I)-2 was reacted at room temperature for 30 minutes, to determine the generation rate of the 211At-labeled compound by TLC (Table 2). Thin-layer chromatography was performed on a 0.2-mm E. Merck silica gel plate (60E-254) and visualized by the imaging plate (IP) system, and ROI was set to the spot (Rf 0.4) of the labeled body (II) for calculation. The developing solvent used was hexane:ethyl acetate=4:1, the IP used was BAS IP SR 2025 E, the exposure time was 2 hours, the IP reader was CD 35 Bio (Elysia-Raytest, Straubenhardt, Germany), and the analysis software was Aida Image Analyzer v.5.1 (Elysia-Raytest, Straubenhardt, Germany).
As shown in Table 2, there was a difference in generation rate depending on the type of the salt used. The generation rate of the labeling precursor (I)-1 was high when using CsHCO3, and the generation rate of the labeling precursor (I)-2 was high when using K2CO3.
The labeling precursor (I)-1 ((2,2-dimethyl-5-((naphthalene-2-ylmethoxy)methyl)-1,3-dioxane-5-yl)methyl(4-methyl)benzene sulfonate) and the labeling precursor (I)-2 (2,2-dimethyl-5-((naphthalene-2-ylmethoxy)methyl)-1,3-dioxane-5-yl)methyl trifluoromethanesulfonate) were synthesized. Further, in order to show synthesis of the 211At-labeled compound (I)-2 is possible, a compound labeled with iodine having similar chemical properties (5-iodomethyl-5-((naphthalene-2-ylmethoxy)methyl)-2,2,-dimethyl-1,3-dioxane) instead of 211At was synthesized.
NMR spectra were recorded with a device, Bruker AVANCE III HD 400 (400 MHz for 1H, 100 MHz for 13C, 373 Hz for 19F), in a solvent shown. Chemical shifts were reported in millions (ppm) relative to the signal of internal tetramethylsilane (δ 0 ppm for 1H) in a CDCl3 solution. NMR spectral data were reported as chloroform-d (7.26 ppm for 1H), DMSO-d6 (2.50 ppm for 1H), CD3OD-d4 (3.31 ppm for 1H), CD3CN-d4 (3.31 ppm for 1H), or chloroform-d (77.16 ppm for 13C), C6H5CF3 (−63.24 ppm for 19F). Multiplicities were reported using the following abbreviations: s, singlet; d, doublet; t, triplet; q, quartet; m, multiplet; br, broad; and J, Hertz coupling constant.
IR spectra were recorded on a Perkin Elmer Spectrum One FT-IR spectrophotometer. Only the most intense and/or structurally important absorptions were reported as IR data in cm−1.
All reactions were monitored by thin-layer chromatography. Thin-layer chromatography was performed on a 0.2 mm E. Merck silica gel plate (60E-254) with UV light and visualized with a p-anisaldehyde solution, cerium sulfate, a ninhydrin ethanol solution, I2—SiO2, or 10% ethanolic phosphomolybdic acid. Merck silica gel 60 (0.063 to 0.200 mm) was used for column chromatography.
ESI TOF mass spectra were measured with Waters LCT Premier (R) XE. HRMS (ESI-TOF) was calibrated with leucine enkephalin (SIGMA) as an internal standard.
Gel permeation chromatography (GPC) for quantitative analysis was performed using a refractive index detector, model RI-5, available from Japan Analytical Industry Co., Ltd., and a ultraviolet light detector, model 310, available from Japan Analytical Industry Co., Ltd., equipped with a polystyrene gel column (JAIGEL-1H, 20 mm×600 mm) using chloroform as a solvent (3.5 mL/min) by model LC 605 (recycle preparative HPLC), available from Japan Analytical Industry Co., Ltd.
Analytical HPLC was performed using an SSC-3461 pump equipped with an SSC-5410 UV detector and a Waters 2475 fluorescence detector.
Using the Glass Contour solvent purification system, dry THF, toluene, MeCN, and CH2Cl2 were obtained. DMF was dried over activated molecular sieves 4A.
To a stirred solution of pentaerythritol (2-4) (10.3 g, 73.4 mmol, 1.00 eq.) in toluene (29.5 mL), were added p-toluenesulfonic acid monohydrate (130.2 mg, 0.734 mmol, 0.0100 eq.) and trimethyl orthoacetate (30.3 mL, 220 mmol, 3.00 eq.) at room temperature. After stirring at room temperature for 18 hours, the reaction mixture was evaporated in vacuo. The residue was used for the next reaction without further purification.
To a stirred solution of the residue in toluene (40.5 mL), was added pentaerythritol (2-4) (10.1 g, 73.4 mmol, 1.00 eq.) at room temperature. After stirring at 130° C. for 11 hours, the reaction mixture was neutralized with NEt3 and evaporated in vacuo. The residue was recrystallized from toluene/Et2O to give 4-(hydroxy methyl)-1-methyl-2,6,7-trioxabicyclo[2,2,2]-octane (2-26) as white crystals (7.17 g, 44.8 mmol, 61%).
1H NMR (400 MHz, CDCl3) δ 4.04 (s, 6H, H-b), 3.47 (d, 2H, H-a, J=3.2 Hz), 1.47 (s, 3H, H-c); 13C NMR (100 MHz, CDCl3) δ 108.6, 69.4, 69.0, 61.3, 35.7, 23.5, 23.4; FT-IR (neat) 3648, 3006, 2952, 2882, 1716, 1541, 1507, 1158, 1038, 870 (cm−1)
To a stirred solution of 60% sodium hydride (3.02 g, 74.9 mmol, 1.20 eq.) washed three times with dry hexane in DMF (16.5 mL), was added a solution of 4-(hydroxy methyl)-1-methyl-2,6,7-trioxabicyclo[2,2,2]-octane (2-26) (10.0 g, 62.4 mmol, 1.00 eq.) in DMF (34.2 mL) at 0° C. The reaction mixture was stirred at room temperature for 1 hour. Then, a solution of 2-(bromomethyl)naphthalene (13.8 g, 62.4 mmol, 1.00 eq.) in DMF (21.2 mL) was added to the reaction mixture at 0° C. After stirring at room temperature for 3 hours, EtOH and water were added to the stirred solution under cooling. The aqueous layer was extracted twice with EtOAc. The combined extracts were washed with brine, dried over MgSO4, filtered, and concentrated in vacuo. The residue was used for the next reaction without further purification.
To the stirred solution of the residue in MeOH (100 mL), was added 3.0 M HCl (10.0 mL) at room temperature. After stirring at 40° C. for 14 hours, the reaction mixture was evaporated in vacuo. The residue was used for the next reaction without further purification.
To the stirred solution of the residue in DMF (27.2 mL), were added CSA (15.6 mg, 0.065 mmol, 0.0012 eq.) and 2,2-dimethoxypropane (8.00 mL, 65.2 mmol, 1.20 eq.) at room temperature. After stirring at 60° C. for 13 hours, the reaction mixture was neutralized with NEt3 and poured into H2O. The aqueous layer was extracted twice with ethyl acetate. The combined extracts were washed with brine, dried over MgSO4, filtered, and concentrated in vacuo. The residue was purified by column chromatography on silica gel using hexane:ethyl acetate (50:50), followed by recrystallization from hexane/EtOAc, to obtain (2,2-dimethyl-5-((naphthalene-2-ylmethoxy)methyl)-1 3-dioxane-5-yl)methanol (2-29) (4.70 g, 14.9 mmol, 24%).
1H NMR (400 MHz, CDCl3) δ 7.86-7.80 (m, 3H, H-aromatic), 7.74 (s, 1H, H-aromatic), 7.50-7.40 (m 3H, H-aromatic), 4.68 (s, 2H, H-f), 3.75 (s, 2H, H-c), 3.74 (s, 2H, H-c), 3.69 (d, 2H, H-b, J=5.8 Hz), 3.59 (s, 2H, H-e), 2.45 (t, 1H, H-a, J=5.3 Hz), 1.41 (s, 3H, H-d), 1.39 (s, 3H, H-d); 13C NMR (100 MHz, CDCl3) δ 135.4, 133.3, 133.2, 128.5, 128.0, 127.8, 126.7, 126.3, 126.1, 125.6, 98.6, 74.0, 72.3, 65.1, 63.0, 39.1, 24.2, 23.5; FT-IR (neat) 3446, 2990, 2870, 1372, 1200, 1081, 1050, 827, 752, 420 (cm−1)
To a stirred solution of (2,2-dimethyl-5-((naphthalene-2-ylmethoxy)methyl)-1,3-dioxane-5-yl)methanol (2-29) (435 mg, 1.39 mmol, 1.00 eq.) in pyridine (7.00 mL), was added p-toluenesulfonyl chloride (532 mg, 2.78 mmol, 2.00 eq.) at room temperature. After stirring at 75° C. for 4.5 hours, the reaction mixture was poured into H2O. The aqueous layer was extracted twice with EtOAc. The combined extracts were washed with brine, dried over MgSO4, filtered, and concentrated in vacuo. The residue was purified by column chromatography on silica gel using hexane:ethyl acetate (80:20), to obtain (2,2-dimethyl-5-((naphthalene-2-ylmethoxy)methyl)-1,3-dioxane-5-yl)methyl(4-methyl)benzene sulfonate (2-16) (530 mg, 1.13 mmol, 41%).
1H NMR (400 MHz, CDCl3) δ 7.84 - 7.75 (m, 5H, aromatic), 7.66 (s, 1H, aromatic), 7.50-7.44 (m, 2H, aromatic) 7.34 (d, 1H, aromatic) 7.26-7.23 (m, 2H, aromatic) 4.55 (s, 2H, H-e) 4.17 (s, 2H, H-a), 3.73 (d, 2H, J=12.0 Hz, H-c), 3.65 (d, 2H, H-c, J=12.0 Hz), 3.40 (s, 2H, H-b), 2.32 (s, 3H, —PhCH3), 1.35 (s, 3H, H-d), 1.28 (s, 3H, H-d); 13C NMR (100 MHz, CDCl3) δ 144.9, 135.5, 133.4, 133.1, 132.7, 129.9, 128.3, 128.2, 128.0, 127.9, 126.3, 126.3, 126.1, 125.5, 98.7, 73.6, 69.4, 68.9, 62.3, 38.8, 25.2, 22.2, 21.7; FT-IR (neat) 2867, 1457, 1362, 1190, 1177, 1088, 977, 815, 666, 476 (cm−1)
To a stirred solution of (2,2-dimethyl-5-((naphthalene-2-ylmethoxy)methyl)-1,3-dioxane-5-yl)methanol (2-29) (50.0 mg, 0.172 mmol, 1.00 eq.) in CH2Cl2 (0.860 mL), was added 2,6-lutidine (60.0 μL, 0.344 mmol, 2.00 eq.) and trifluoromethanesulfone acid anhydride (40.0 μL, 0.206 mmol, 1.20 eq.) at 0° C. After stirring at 0° C. for 0.5 hours, the reaction mixture was poured into a saturated NH4Cl aqueous solution. The aqueous layer was extracted twice with EtOAc. The combined extracts were washed with brine, dried over MgSO4, filtered, and concentrated in vacuo. The residue was purified by column chromatography on silica gel using hexane:EtOAc (80:20), to obtain (2,2-dimethyl-5-((naphthalene-2-ylmethoxy)methyl)-1,3-dioxane-5-yl)methyl trifluoromethanesulfonate (2-18) (68.0 mg, 0.152 mmol, 88%).
1H NMR (400 MHz, CDCl3) δ 7.85-7.81 (m, 3H, aromatic), 7.72 (s, 1H, aromatic), 7.51-7.39 (m, 3H, aromatic), 4.77 (s, 2H, H-a), 4.64 (s, 2H, H-e), 3.79 (d, 2H, J=12.4 Hz, H-c), 3.71 (d, 2H, J=12.4 Hz, H-c) 3.37 (s, 2H, H-b) 1.39 (s, 6H, H-d); 13C NMR (100 MHz, CDCl3) δ 135.1, 133.3, 133.2, 128.5, 128.0, 127.9, 126.7, 126.4, 126.2, 125.7, 99.0, 75.8, 73.9, 68.4, 62.1, 39.2, 26.5, 20.9; 19F NMR (373 MHz, CDCl3) δ-75.2; FT-IR (neat) 2993, 2872, 1415, 1374, 1246, 1203, 1146, 1087, 941, 824, 617, 477 (cm−1)
To a stirred solution of (2,2-dimethyl-5-((naphthalene-2-ylmethoxy)methyl)-1,3-dioxane-5-yl)methyl trifluoromethanesulfonate (2-18) (10.0 mg, 0.0223 mmol, 1.00 eq.) in CH3CN (0.300 mL), was added sodium iodine (7.70 mg, 0.0514 mmol, 2.30 eq.) at room temperature. After stirring at room temperature for 1 hour, the reaction mixture was poured into H2O. The aqueous layer was extracted twice with EtOAc. The combined extracts were washed with brine, dried over MgSO4, filtered, and concentrated in vacuo. The residue was purified by short-path column chromatography on silica gel using EtOAc, to obtain 5-iodomethyl-5-((naphthalene-2-ylmethoxy)methyl)-2,2,-dimethyl-1,3-dioxane (2-17) (9.5 mg, 0.0223 mmol, quant.).
1H NMR (400 MHz, CDCl3) δ 7.85-7.83 (m, 3H, aromatic), 7.77 (s, 1H, aromatic), 7.50-7.45 (m, 3H, aromatic), 4.67 (s, 2H, H-e), 3.82 (d, 2H, H-c, J=12.0 Hz), 3.72 (d, 2H, H-c, J=12.0 Hz), 3.51 (s, 2H, H-a or H-b), 3.42 (s, 2H, H-a or H-b), 1.41 (s, 3H, H-d), 1.39 (s, 3H, H-d); 13C NMR (100 MHz, CDCl3) 6 135.7, 133.4, 133.2, 128.3, 128.0, 127.8, 126.5, 126.3, 126.0, 125.8, 98.7, 73.8, 71.3, 65.0, 37.3, 29.8, 23.8, 23.7, 11.7; FT-IR (neat) 2923, 2863, 1717. 1505, 1370, 1270, 1092, 834, 742, 451 (cm−1)
211At labeled metaastatobenzylguanidine (211At-MABG) was synthesized under the following two types of reaction conditions. An 211At solution dissolved in 90.9 μL of MeOH containing 0.5 mg of K2CO3 was put into a reaction container, a vent needle connected to activated carbon was attached, and the solvent was removed with a nitrogen gas. Conditions (1): 50 μL of trifluoroacetic acid (TFA) containing 0.4 mg of N-chlorosuccinimide (NCS) and 50 μL of TFA containing 0.1 mg of a labeling precursor, metatrimethylsilyl benzyl guanidine (MTMSBG) were added thereto, or conditions (2): TFA (50 μL) and TFA (50 μL) containing 0.1 mg of a precursor, MTMSBG, were added thereto. Then, a vent needle connected to activated carbon was attached after heating at 70° C. for 10 minutes, and TFA was removed by spraying a nitrogen gas under heating at 70° C. The reaction product was dissolved in 0.5 mL of distilled water and passed through a Sep-Pak tC18 Light (duplicate) column preactivated with 3 mL of ethanol (EtOH) and 6 mL of water for injection. It was washed with 0.5 mL×2 of water for injection, eluted with 0.5 mL×4 of 5% EtOH, and further eluted with 1.0 mL×2 of 5% EtOH, each fraction was collected in a vial, and radioactivity was measured (Table 3). HPLC was also used to measure the MABG purity of each fraction (Table 4).
MTMSBG was purchased from ABX, Prominence, available from SHIMADZU CORPORATION, was used for HPLC, SPD-M20A (available from SHIMADZU CORPORATION) was used for UV detection, and GABI STAR (Raytest) was used for radioactivity analysis. The analysis conditions were as follows. The elution time of 211At-MABG was 8.2 minutes.
From Table 3, the radiochemical yield after concentration of 211At was 67.3% with NCS (collecting product vial 2-6) and 75.1% without NCS (collecting product vial 2-5). The labeling synthesis of 211At-MABG was result in good yields regardless of the presence or absence of the oxidant NCS.
From Table 4, the radiochemical purity was 97.7% with NCS (collecting product vial 2-6) and 95.5% without NCS (collecting product vial 2-5). The radiochemical purity of the 211At-MABG to be obtained was high regardless of the presence or absence of the oxidant NCS.
All publications, patents, and patent applications cited herein are hereby incorporated by reference in their entirety.
The present invention relates to a method for producing astatine-211, and therefore it can be used in industrial fields for producing pharmaceuticals or the like using astatine-211.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2020-081819 | May 2020 | JP | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/JP2021/017415 | 5/6/2021 | WO |
