WO2006101082A1 - ピリミジン化合物の結晶、非晶質および製造方法 - Google Patents
ピリミジン化合物の結晶、非晶質および製造方法 Download PDFInfo
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- WO2006101082A1 WO2006101082A1 PCT/JP2006/305565 JP2006305565W WO2006101082A1 WO 2006101082 A1 WO2006101082 A1 WO 2006101082A1 JP 2006305565 W JP2006305565 W JP 2006305565W WO 2006101082 A1 WO2006101082 A1 WO 2006101082A1
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- furyl
- amino
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- pyrimidine
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/10—Laxatives
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
Definitions
- the present invention relates to a crystal, an amorphous form and a production method of a pyrimidine compound. More specifically, the present invention is a compound effective for the prevention and treatment of various diseases such as constipation.
- 5- [2-Amino_4_ (2-furyl) pyrimidine-5_yl] _1_methylpyridine_2 5_ [2—Amino-4_ (2_furyl) pyrimidine-5_yl] _ 1 _Methylpyridine _ 2 (1H) On Regarding the crystals of hydrates and the process for their preparation, the followings are related: 5- [2-Amino-1-4- (2-furyl) pyrimidin-1-5-yl] -1-methylpyridin_2 (1H) -one amorphous and its preparation Regarding the method.
- the present invention also relates to a method for producing a pyrimidine compound such as 5- [2-amino-1-4_ (2-furyl) pyrimidine-5_yl] _1_methylpyridine_2 (1H) -one and an intermediate.
- a pyrimidine compound such as 5- [2-amino-1-4_ (2-furyl) pyrimidine-5_yl] _1_methylpyridine_2 (1H) -one and an intermediate.
- a method for producing 5_ [2-amino-4_ (2-furyl) pyrimidin-5_yl] _1_methylpyridin_2 (1H) -one disclosed in Patent Document 1 has the following reaction scheme 2- (6—Black mouth 3_pyridyl) _ 3—Dimethylamino 1_ (2-furyl) _2_propene_1_one reacts with guanidine 5_ (6_Black mouth 3 _Pyridyl) _4_ (2-Furyl) 1-2-pyrimidinylamine is obtained and oxidized to give 5- [2-amino-1- (2-furyl) -5-pyrimidinyl] -1, 2, 2 dihydro-1 This method obtains pyridinone and methylates it.
- Patent Document 1 describes the following reaction formula as general production method D c
- R ld represents a C6-14 aromatic hydrocarbon cyclic group, a 5- to 14-membered aromatic heterocyclic group, and the like.
- the reaction in which R ld is N-alkylpyridone is specifically disclosed. It has not been.
- Patent Document 1 Pamphlet of International Publication No. 03/035639
- an active ingredient of a medicine needs to stably supply a product of a certain quality. Therefore, when the active pharmaceutical ingredient is obtained as a crystalline substance, it consists of a single crystal form and is soluble. It is desirable to have good physical properties such as excellent solution. Therefore, an object of the present invention is to produce crystals of 5- [2-amino-1- (2-furyl) pyrimidine-1-yl] -1-methinolepyridin-2- (1H) -one having favorable physical properties. Is to provide.
- Alkyl halides are easily decomposed in the presence of a base, and therefore the power that requires more than one equivalent to the starting material Alkyl halides are toxic and there is a demand to reduce the amount used. Therefore, another object of the present invention is to have the advantage that the number of steps is small and the amount of alkyl halide used is small. 5_ [2-Amino-4- (2-furyl) pyrimidine-5-yl] -1-methylpyridine It is to provide a method for producing pyrimidine compounds such as 1 (1H) -one.
- 13 C solid-state nuclear magnetic resonance spectrum (hereinafter referred to as 13 C solid-state NMR spectrum), it has a peak at a chemical shift of about 134 ⁇ 9 ppm and / or about 14 ⁇ 3 ppm.
- R represents a CI 6 alkyl group
- R 2 and R 3 each independently represent a hydrogen atom or a C 16 alkyl group.
- R 1 represents a C 16 alkyl group.
- R represents a C16 alkyl group
- X represents a halogen atom
- C-type crystals of 5- [2-amino-4 (2-furyl) pyrimidin-5-yl] 1 methylpyridin-2 (1H) -one of the present invention (hereinafter also simply referred to as C-type crystals)
- 5- [2 Amino-4 mono (2-furyl) pyrimidine 5-yl] 1 methylpyridin 2 (1H) -one hydrate crystals (hereinafter also referred to simply as hydrate crystals)
- 5- [2 amino-4 mono (2-furyl) ) Pyrimidine-5-yl] 1 Methylpyridin 2 (1H) -one amorphous (hereinafter also simply referred to as amorphous) has good physical properties such as excellent solubility, constipation, etc.
- amorphous has good physical properties such as excellent solubility, constipation, etc.
- amorphous has good physical properties such as excellent solubility, constipation, etc.
- amorphous has good physical properties such as excellent solubility
- the method for producing a pyrimidine compound such as 5- [2 amino-4 (2furyl) pyrimidin-5-yl] -1 methylpyridin-2 (1H) -one of the present invention has a small number of steps. This has the advantage that the amount of alkynole halide used is small, which is industrially advantageous.
- FIG. 1 is a diagram showing a powder X-ray diffraction pattern of the crystal obtained in Comparative Example 1.
- FIG. 2 is a diagram showing a powder X-ray diffraction pattern of the crystal obtained in Comparative Example 2.
- FIG. 3 is a view showing a powder X-ray diffraction pattern of the crystal obtained in Comparative Example 3.
- FIG. 4 is a view showing a powder X-ray diffraction pattern of the crystal obtained in Example 4A.
- FIG. 5 is a diagram showing a powder X-ray diffraction pattern of the crystals obtained in Example 5.
- FIG. 6 is a view showing an amorphous powder X-ray diffraction pattern obtained in Example 6.
- FIG. 7 is a view showing a temperature change of a powder X-ray diffraction pattern of the crystal obtained in Comparative Example 1.
- FIG. 8 is a view showing a temperature change of a powder X-ray diffraction pattern of the crystal obtained in Comparative Example 3.
- FIG. 9 is a view showing a temperature change of a powder X-ray diffraction pattern of the crystal obtained in Example 4A.
- FIG. 10 is a diagram showing DSC patterns of crystals obtained in Comparative Example 1, Comparative Example 3 and Example 4A.
- Figure 11 shows the DSC pattern 40-230 of Figure 10. It is an enlarged view of the range of C.
- FIG. 12 is a view showing an amorphous DSC pattern obtained in Example 6.
- FIG. 13 is a diagram showing a 13 C solid-state NMR spectrum of the crystal obtained in Comparative Example 3.
- FIG. 14 is a diagram showing a 13 C solid-state NMR spectrum of the crystal obtained in Example 4A.
- FIG. 15 is a diagram showing an infrared absorption spectrum of the crystal obtained in Comparative Example 3.
- FIG. 16 is a diagram showing an infrared absorption spectrum of the crystal obtained in Example 4A.
- FIG. 17 is a graph showing the results of Test Example 1. BEST MODE FOR CARRYING OUT THE INVENTION
- the 5_ [2-amino-4_ (2_furyl) pyrimidine-5_yl] _1_methylpyridin_2 (1H) -one crystal (C-type crystal) of the present invention is diffracted by powder X-ray diffraction. Characterized by diffraction peaks at angles (2 ⁇ ⁇ 0.2 °) 9.7 ° and Z or 21.9 °, and peaks at chemical shifts of about 134.9 ppm and / or about 14 6.3 ppm in 13 C solid state NMR spectra It is characterized by that. These characteristic peaks in the powder X-ray diffraction and 13 C solid state NMR vectors are not observed in the crystal described in Example 16 of Patent Document 1 (B-type crystal).
- FIGS. 4 and 9 Typical powder X-ray diffraction patterns and 13 C solid state NMR spectra of C-type crystals are shown in FIGS. 4 and 9, respectively.
- Figure 16 shows a typical infrared absorption spectrum of the C-type crystal.
- C-type crystals are more soluble than B-type crystals.
- the present invention also includes a crystal in which the diffraction angle of the peak coincides with an error of ⁇ 0.2 ° only by the crystal in which the diffraction angle of the peak in powder X-ray diffraction is completely identical.
- “having a diffraction peak at a diffraction angle (2 ⁇ ⁇ 0.2 °) of 9.7 °” means “a diffraction peak within a range of diffraction angle (2 ⁇ ) of 9.5 ° to 9.9 °.
- Means "having a diffraction peak at a diffraction angle (2 ⁇ ⁇ 0.2 °) of 21.9 °” means “having a diffraction peak within the range of diffraction angle (2 ⁇ ) of 21.7 ° to 22.1 °” Means that.
- “having a diffraction peak at diffraction angle (2 ⁇ ⁇ 0.2 °) 9.7 ° and ⁇ or 21.9 °” means having at least one diffraction peak among the above diffraction peaks.
- the method for producing the above-mentioned C-type crystal of the present invention is characterized in that the amorphous form of 5_ [2-amino-4_ (2_furyl) pyrimidin_5_yl] -1-methylpyridin_2 (1H) -one is highly enhanced. It is characterized by heating and drying in a temperature range.
- the amorphous form of 5- [2-amino-1- (2-furyl) pyrimidin-1-yl] -1-methylpyridin-2 (1H) -one can be obtained by the production method described later.
- Heat drying in a high temperature region means standing for 12 to 24 hours at a temperature of 40 to 80 ° C, and preferably standing at 60 ° C for 20 hours.
- the 5_ [2-amino-4_ (2_furyl) pyrimidine-5_yl] _1_methylpyridin-2- (1H) -one hydrate crystals of the present invention are preferably monohydrate crystals. And preferably has a diffraction peak at a diffraction angle (2 ⁇ ⁇ 0.2 °) of 8.8 ° in powder X-ray diffraction. A typical powder X-ray diffraction pattern of hydrate crystals is shown in FIG. Hydrate crystals are more soluble than B-type crystals.
- the method for producing the hydrate crystal according to the present invention comprises a C-type crystal of 5- [2-amino-4-mono (2-furyl) pyrimidin-1-5-yl] -1-methylpyridin-2- (1H) -one. It is characterized by humidifying.
- the humidification condition means that the relative humidity is kept at 90 to 100% in an atmosphere maintained for 12 to 36 hours at 1 to 30 ° C, preferably nitrogen having a relative humidity of 95%. Leave at 1-30 ° C for 24 hours in an atmosphere. Further, humidification is preferably performed under a nitrogen stream.
- amorphous 5_ [2-amino-4_ (2_furyl) pyrimidine-5_yl] _1_methylpyridin-2 (1H) -one of the present invention is more soluble than the B-type crystal. . [0028] Method for producing amorphous soot
- the above amorphous production method of the present invention is characterized by freeze-drying a solution of 5- [2 amino-4 (2 furyl) pyrimidin 5-yl] 1 methylpyridin 2 (1H) -one.
- a mixed solvent of an alcohol solvent such as methanol, ethanol, t-butyl alcohol and water
- a mixed solvent of t-butyl alcohol and water more preferred is a mixed solvent of t-butyl alcohol and water, and most preferred is t-butyl alcohol and water.
- Lyophilization can be performed under conditions generally known to those skilled in the art. For example, after freezing the solution, the temperature is gradually or gradually increased from about 80 ° C to about room temperature in a freeze dryer.
- Patent Document 1 [2-Amino 1 4_ (2_furyl) pyrimidine 1 5 _ 1] _ 1 _Methylpyridine 1 2 (1 ⁇ ) _On as a therapeutic agent for constipation is disclosed in detail in Patent Document 1
- C-type crystals, hydrate crystals, and amorphous can be used as active ingredients of therapeutic agents for constipation.
- the entire disclosure of Patent Document 1 is included in the disclosure of this specification as a reference.
- C-type crystals, hydrate crystals, and amorphous are useful as an active ingredient in the treatment of constipation because of their good stability and physical properties.
- Pyrimidine-5-yl]-1-methylviridin-2 (1H) -one is the most suitable form for use.
- C-type crystals, hydrate crystals, or amorphous are conventionally used in the form of tablets, powders, granules, granules, coated tablets, capsules, syrups, U lozenges, inhalation. Preparations, suppositories, injections, ointments, eye ointments, eye drops, nasal drops, ear drops, poultices, lotions and the like.
- excipients binders, lubricants, coloring agents, flavoring agents, and stabilizers, emulsifiers, absorption promoters, surfactants, pH adjusters, preservatives as necessary Antioxidants and the like can be used, and they are generally formulated by blending ingredients used as raw materials for pharmaceutical preparations.
- Examples of these components include animal and vegetable oils such as soybean oil, beef tallow, and synthetic glycerides; hydrocarbons such as liquid paraffin, squalene, and solid paraffin; ester oils such as octyldodecyl myristate and isopropyl myristate; Alcohol, higher alcohols such as behenyl alcohol; silicone resin; silicone oil; polyoxyethylene fatty acid ester ester, sorbitan fatty acid ester, glycerin fatty acid ester, polyoxyethylene sorbitan fatty acid ester, polyoxyethylene hydrogenated castor oil, polyoxyethylene Surfactants such as polyoxypropylene block copolymers; hydroxyethyl cellulose, polyacrylic acid, carboxyvinyl polymer, polyethylene glycol, polyvinyl pyrrolidone, methyl cellulose Water-soluble polymers such as ethanol, isopropyl alcohol and the like lower alcohols; glycerin, propylene glycol, dipropyl alcohol and
- excipients include lactose, corn starch, sucrose, glucose, mannitol, sorbitol, crystalline cellulose, silicon dioxide, and the like
- binders include polybular alcohole, polyvinylinoatenole, methinoresenololose , Ethinoresenololose, gum arabic, tragacanth, gelatin, shellac, hydroxypropylmethylcellulose, hydroxypropenolecellulose, polybulurpyrrolidone, polypropylene glycol, polyoxyethylene, block polymer, medalmin, etc.
- starch for example, starch, agar, gelatin powder, crystalline cellulose, calcium carbonate, sodium bicarbonate, calcium citrate, dextri Pectin, carboxymethylcellulose 'calcium isostatics
- lubricants for example, magnesium stearate, talc, polyethylene glycol, silica, hydrogenated vegetable oils, etc., which are permitted to be added to pharmaceuticals as coloring agents
- S and a flavoring agent include cocoa powder, heart beaten brain, fragrance powder, heart force oil, dragon brain, cinnamon powder and the like.
- these tablets and granules may be appropriately coated with sugar coating or other necessary.
- liquid preparations such as syrups and injectable preparations
- pH adjusters, solubilizers, tonicity agents, etc. are necessary for C-type crystals, hydrate crystals or amorphous forms.
- the method for producing the external preparation is not limited and can be produced by a conventional method. That is, as a base material used for formulation, various raw materials usually used for pharmaceuticals, quasi drugs, cosmetics, etc. can be used. Specific examples of base materials to be used include animal and vegetable oils, mineral oils, ester oils, waxes, higher alcohols, fatty acids, silicone oils, surfactants, phospholipids, alcohols, and polyhydric alcohols. Raw materials such as water-soluble polymers, clay minerals, and purified water, and pH adjusters, antioxidants, chelating agents, antiseptic / antifungal agents, coloring agents, fragrances, etc. are added as necessary. Power that can be used The base material of the external preparation that is useful in the present invention is not limited thereto.
- components such as blood flow promoters, bactericides, anti-inflammatory agents, cell activators, vitamins, amino acids, humectants, keratolytic agents and the like can be blended as necessary.
- the amount of the base material added is usually an amount that is set in the production of the external preparation.
- a C-type crystal, hydrate crystal or amorphous When a C-type crystal, hydrate crystal or amorphous is administered, its form is not particularly limited, and it may be orally or parenterally administered by a commonly used method.
- the dosage of the medicament according to the present invention is determined by the patient's age, sex, weight, and symptoms. It can be selected as appropriate according to the degree of the disease, the specific type of the disease, the dosage form, the type of salt, and the like.
- lOO xg dose 500 mg, more preferably 100 ⁇ g dose, 30 mg is administered in one or several divided doses.
- R 1 represents a C1-6 alkyl group
- R 2 and R 3 each independently represent a hydrogen atom or a C16 alkyl group.
- This manufacturing method has an advantage that the number of steps is small as compared with the conventional manufacturing method (the manufacturing method described in Patent Document 1).
- Cl 6 alkyl group for example, methyl, ethyl, n-propyl, isopropylinole, n-butyl, isobutyl, sbutyl, t-butyl, n pentyl, isopentyl, s-pentyl, t pentyl, 2 —Methylbutyl, 1-methylbutyl, 2-methylbutyl, neopentyl, 1,1-dimethylpropyl, 1,2-dimethylpropyl, 1-ethylpropyl, n-hexyl, isohexyl, 4-methylpentyl, 3-methylpentyl, 2-methylpentyl , 1-methylpentyl, 3, 3 dimethylbutyl, 2, 2 dimethylbutyl, 1, 1-dimethylbutyl, 1,2-dimethylbutyl, 1,3-dimethylbutyl, 2, 3_dimethylolbutyl, 1-ethyl,
- R 1 is preferably a methyl group.
- R 2 and R 3 are preferably hydrogen atoms.
- the solvent used in the reaction of compound (II) and compound (III) is not particularly limited as long as it dissolves the starting material to some extent and does not inhibit the reaction.
- N, N-dimethylformamide, 1_methyl_2_pyrrolidone, N, N'-dimethylindanone, acetritolyl and the like can be mentioned.
- Compound (III) can be used in an amount of 1.0 to 3.0 equivalents relative to Compound (II). 1, 8 Diazabicyclo [5. 4. 0]
- the reaction may be carried out in the presence of a base such as 7 7
- the base can be used in an amount of 1.5 to 3.0 equivalents relative to compound (II).
- the reaction time is 1.5 to 48 hours.
- the reaction temperature is 25-80 ° C.
- R represents a CI 6 alkyl group.
- N dimethylformamide dimethylacetal are preferably obtained by reacting them.
- the solvent used in the reaction of compound (IV) with N, N dimethylformamide dimethylacetal is not particularly limited as long as it dissolves the starting material to some extent and does not inhibit the reaction. Examples thereof include N, N dimethylformamide, 1-methyl-2-pyrrolidone, N, N′-dimethylindanone, and acetritolyl.
- N, N-dimethylformamide dimethyl acetal can be used in an amount of 1.5 to 3.0 equivalents relative to compound (IV).
- the reaction time is 2 to 22 hours.
- the reaction temperature is 60-80 ° C.
- compound (III) was added to the reaction solution in which compound (IV) was reacted with N, N dimethylformamide dimethyl acetal to produce compound (II), and compound (II I) may be obtained.
- R 1 represents a C 16 alkyl group.
- R represents a CI 6 alkyl group, and X represents a halogen atom.
- the halogen atom is a fluorine atom, a chlorine atom, a bromine atom or an iodine atom.
- R is preferably a methyl group, and X is preferably an iodine atom.
- the solvent used in the reaction between the compound (V) and the compound (VI) is not particularly limited as long as it dissolves the starting material to some extent and does not inhibit the reaction. Examples include N, N-dimethylformamide, 1_methyl_2_pyrrolidone, N, N'-dimethylindanone, dimethyl sulfoxide, t_butyl alcohol and the like.
- the compound (VI) is preferably used in a catalytic amount relative to the compound (V), more preferably from 0.3 to 1.0 equivalent.
- the reaction time is 3-7 hours.
- the reaction temperature is 80 ⁇ : 100 ° C.
- R 1 represents a C 16 alkyl group
- Y represents a leaving group
- Y represents a leaving group such as a halogen atom, a mesyloxy group or a trifluoromethyloxy group, and is preferably a chlorine atom, more preferably a chlorine atom.
- Q is preferably a morpholino group.
- a starting material is used to some extent. There is no particular limitation as long as it dissolves and does not inhibit the reaction, and examples thereof include tetrahydrofuran, 1,2-dimethoxyethane, t-butylmethyl ether, and toluene.
- Compound (VIII) can use 1 ⁇ 05-1.15 equivalents of Compound (VII).
- the reaction may be carried out in the presence of a base such as potassium t-butoxide.
- the base can be used in an amount of 1.05 to 1.15 equivalents relative to compound (II).
- the reaction time is:! ⁇ 3 hours.
- the reaction temperature is _20-0 ° C.
- compound (I) is 5_ [2-amino-4_ (2_furyl) pyrimidin _5-yl] _1-methylpyridine-2 (1H) -one
- the following compounds are useful as intermediates: Yes: 5_ [2 —dimethylamino 1- (furan-2-carbonyl) one bur] — 1-methyl-1 1H-pyridin-2-one, 5_ (2-furan-2-inole 2_oxoethyl) _1_ Methyl _1H_pyridin-2-one and 1-furan _ 2 _inole-2- (6-methoxy monopyridine _ 3 ⁇ ynole) monoethanone.
- Furan-2 Inole 3 (6 Methoxy monopyridine-3-Inole) —2 Monorephorin—4 Loop loop pionate (6)
- DME 1,2 Dimethoxyethane
- Example 3B Synthesis of 5 — “2-Amino 1 4 _ (2 _ Furyl) Pyrimidine 1 5 _il ⁇ _ 1 _Methylolepiridin 1 2 (1H) —one (10)
- Example 3 Crude 5- [2-amino- 4- (2-furyl) pyrimidine-5-yl]-1 -methyl pyridine 2 (1H) -one (10) 30 g of 2-propanol 30 mL and 150 mL of water were added, and the mixture was heated and stirred in a 90 ° C oil bath for 25 minutes. After confirming that there was no solid matter, filtration was performed while hot, and the filtrate was heated and stirred at 70 ° C for about 30 minutes. Subsequently, the reaction solution was stirred with heating at an external temperature of 55 ° C for 1.3 hours, and further stirred at an external temperature of 45 ° C to 40 ° C for 2.3 hours.
- the crystal (A-type crystal) (5.43 g) obtained in Comparative Example 1 was dissolved in t_butyl alcohol Z water (1: 1, v / v) lL and filtered. Next, the obtained filtrate is put into a freeze dryer and freeze-dried. It was. Freeze-drying time and temperature conditions are as follows.
- the amorphous substance was obtained by removing from the freeze dryer. Next, the obtained amorphous substance (total amount) was left in an oven at 60 ° C. for about 20 hours to obtain C-type crystals.
- Hydrated crystals were obtained by standing at room temperature for 4 hours.
- Example 6 Production of amorphous soot
- Amorphous material was obtained by removing from the freeze dryer.
- Tube current Tube voltage: CuZ40kVZ200mA
- DSC analysis was carried out under the following conditions using about 3 mg of each of the crystals (A-type crystal, B-type crystal (2) and C-type crystal) obtained in Comparative Example 1, Comparative Example 3 and Example 4A. .
- the DSC pattern of each crystal is shown in Fig. 10 and Fig. 11 (enlarged view in the range of 40 to 230 ° C). Further, DSC analysis was carried out under the same conditions using about 4 mg of the amorphous material obtained in Example 6.
- An amorphous DSC pattern is shown in FIG. The endothermic peaks and exothermic peaks are summarized in Table 4.
- Measuring instrument DSC822 E manufactured by METTLER TOLEDO
- A-type crystal endothermic peak around 2 48 ° C
- the 13 C solid state NMR spectra of the crystals (B type crystal (2) and C type crystal) obtained in Comparative Example 3 and Example 4 were measured under the following conditions.
- the 13 C solid state NMR spectrum of each crystal is shown in FIGS. 13 and 14.
- the chemical shift of each crystal is summarized in Table 5.
- B-type crystals had characteristic peaks at 110.6 ppm and 117.2 ppm
- C-type crystals had characteristic peaks at 133.9 ppm and 146.3 ppm.
- Measuring device FT / IR—620 (JASCO)
- Measurement method ATR method Measuring range: 4000cm ⁇ 650cm
- the collected solution was filtered with a filter (0.2 zm), and 5 _ [2—amino _4_ (2-furinole) pyrimidine 1 _yl] -1 1-methylpyridine 1 2 (1H) —
- the ON concentration was measured by HPLC.
- the HPLC conditions are as follows. The obtained results are shown in FIG. (HPLC conditions)
- the present invention consists of a single crystal form and excellent solubility, 5- [2-amino-4- (2-furolole) pyrimidine-5-yl] -1-methylviridine-2- ( 1H) —one crystal (C-type crystal) and method for producing the same.
- the present invention also comprises a single crystalline form, excellent solubility, 5- [2-amino- (2-furyl) pyrimidine-5-yl] -1-methylpyridine-2 (1H) —Provides crystals of on-hydrate and methods for producing the same.
- the present invention also provides dissolution
- the present invention provides an amorphous 5- [2 amino-4 (2furyl) pyrimidine 5-yl] 1 methylpyridin 2 (1H) -one having excellent properties and a method for producing the same. These crystals and amorphous are suitable for use as an active ingredient of a pharmaceutical composition, particularly as an active ingredient of a therapeutic agent for constipation.
- the present invention has a small number of steps and uses a small amount of alkyl halide, such as 5_ [2-amino-4_ (2 furyl) pyrimidine-5_yl] _1_methylpyridine_2 (1H) -one.
- a manufacturing method is provided. A powerful manufacturing method is industrially advantageous.
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Abstract
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Priority Applications (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP06729533A EP1862463A4 (en) | 2005-03-21 | 2006-03-20 | PYRIMIDINE COMPOSITE CRYSTAL OR AMORPHIC FORM AND METHOD OF MANUFACTURING THEREOF |
CN2006800019726A CN101103024B (zh) | 2005-03-21 | 2006-03-20 | 嘧啶化合物的结晶、无定形物及制备方法 |
CA002596737A CA2596737A1 (en) | 2005-03-21 | 2006-03-20 | Pyrimidine compound crystal or amorphous form and process for producing the same |
AU2006225700A AU2006225700B2 (en) | 2005-03-21 | 2006-03-20 | Pyrimidine compound crystal or amorphous form and process for producing the same |
JP2007509274A JPWO2006101082A1 (ja) | 2005-03-21 | 2006-03-20 | ピリミジン化合物の結晶、非晶質および製造方法 |
IL184984A IL184984A0 (en) | 2005-03-21 | 2007-08-01 | Pyrimidine compound crystal or amorphous form and process for producing the same |
IL209568A IL209568A (en) | 2005-03-21 | 2010-11-25 | Process for preparing 5-[2-amino-4-(2-furyl)pyrimidin-5-yl]-1-methylpyridin-2(1h)-one and derivatives thereof |
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US66358005P | 2005-03-21 | 2005-03-21 | |
US60/663580 | 2005-03-21 |
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PCT/JP2006/305565 WO2006101082A1 (ja) | 2005-03-21 | 2006-03-20 | ピリミジン化合物の結晶、非晶質および製造方法 |
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EP (3) | EP1840128A4 (ja) |
JP (2) | JP5027654B2 (ja) |
KR (2) | KR20070112381A (ja) |
CN (3) | CN101928282B (ja) |
AU (2) | AU2006225700B2 (ja) |
CA (2) | CA2596735C (ja) |
IL (3) | IL184983A (ja) |
WO (2) | WO2006101081A1 (ja) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
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WO2008029876A1 (fr) * | 2006-09-07 | 2008-03-13 | Eisai R & D Management Co., Ltd. | Sel de 5-[2-amino-4-(2-furyl)pyrimidin-5-yl]-1-méthylpyridin-2(1h)-one et un cristal de celui-ci |
WO2016171254A1 (ja) * | 2015-04-22 | 2016-10-27 | 日本ケミファ株式会社 | 2-[3-シアノ-4-(2-メチルプロポキシ)フェニル]-4-メチルチアゾール-5-カルボン酸の結晶、その製造方法、及びそれらの利用 |
JP2017165787A (ja) * | 2012-12-22 | 2017-09-21 | 山▲東▼亨利医▲薬▼科技有限▲責▼任公司 | ミネラルコルチコイド受容体拮抗剤としての化合物の結晶形及びその調製方法 |
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TWI426074B (zh) * | 2008-04-30 | 2014-02-11 | Nerviano Medical Sciences Srl | 5-(2-胺基-嘧啶-4-基)-2-芳基-1h-吡咯-3-羧醯胺之製造方法 |
DE102009041241A1 (de) | 2009-09-11 | 2011-08-04 | Bayer Schering Pharma Aktiengesellschaft, 13353 | Substituierte Aryl-Verbindungen und ihre Verwendung |
CN104684900B (zh) | 2012-10-25 | 2017-04-12 | 沈阳中化农药化工研发有限公司 | 取代嘧啶类化合物及其用途 |
CN107963991A (zh) * | 2017-12-29 | 2018-04-27 | 成都百裕制药股份有限公司 | 一种无定形托伐普坦的生产方法 |
CN110240593A (zh) * | 2018-03-09 | 2019-09-17 | 四川科伦博泰生物医药股份有限公司 | 取代芳胺化合物及其制备方法和用途 |
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WO2003035639A1 (fr) | 2001-10-22 | 2003-05-01 | Eisai Co., Ltd. | Compose de pyrimidine et composition medicinale contenant ledit compose |
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JP3901882B2 (ja) * | 1999-09-03 | 2007-04-04 | 大日本インキ化学工業株式会社 | 新規キノリノン誘導体製剤及びその製造方法 |
JP3547009B1 (ja) * | 2002-12-27 | 2004-07-28 | 小野薬品工業株式会社 | 5−[(1z,2e)−2−メチル−3−フェニル−2−プロペニリデン]−4−オキソ−2−チオキソ−3−チアゾリジン酢酸の新規結晶、その製造方法およびその結晶を有効成分とする医薬 |
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- 2006-03-20 CA CA002596737A patent/CA2596737A1/en not_active Abandoned
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WO2003035639A1 (fr) | 2001-10-22 | 2003-05-01 | Eisai Co., Ltd. | Compose de pyrimidine et composition medicinale contenant ledit compose |
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Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2008029876A1 (fr) * | 2006-09-07 | 2008-03-13 | Eisai R & D Management Co., Ltd. | Sel de 5-[2-amino-4-(2-furyl)pyrimidin-5-yl]-1-méthylpyridin-2(1h)-one et un cristal de celui-ci |
JP2017165787A (ja) * | 2012-12-22 | 2017-09-21 | 山▲東▼亨利医▲薬▼科技有限▲責▼任公司 | ミネラルコルチコイド受容体拮抗剤としての化合物の結晶形及びその調製方法 |
WO2016171254A1 (ja) * | 2015-04-22 | 2016-10-27 | 日本ケミファ株式会社 | 2-[3-シアノ-4-(2-メチルプロポキシ)フェニル]-4-メチルチアゾール-5-カルボン酸の結晶、その製造方法、及びそれらの利用 |
JPWO2016171254A1 (ja) * | 2015-04-22 | 2018-03-22 | 日本ケミファ株式会社 | 2−[3−シアノ−4−(2−メチルプロポキシ)フェニル]−4−メチルチアゾール−5−カルボン酸の結晶、その製造方法、及びそれらの利用 |
JP7164926B2 (ja) | 2015-04-22 | 2022-11-02 | 日本ケミファ株式会社 | 2-[3-シアノ-4-(2-メチルプロポキシ)フェニル]-4-メチルチアゾール-5-カルボン酸の結晶、その製造方法、及びそれらの利用 |
Also Published As
Publication number | Publication date |
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AU2006225700B2 (en) | 2011-09-01 |
CA2596735A1 (en) | 2006-09-28 |
EP2210889A1 (en) | 2010-07-28 |
AU2006225699A1 (en) | 2006-09-28 |
CN101928282B (zh) | 2012-02-29 |
CN101103024B (zh) | 2011-03-16 |
EP1862463A4 (en) | 2009-07-22 |
CA2596735C (en) | 2013-01-08 |
KR20070112368A (ko) | 2007-11-23 |
IL209568A0 (en) | 2011-01-31 |
IL184983A (en) | 2011-12-29 |
AU2006225699B2 (en) | 2011-02-24 |
JPWO2006101082A1 (ja) | 2008-09-04 |
EP1840128A1 (en) | 2007-10-03 |
CN101103025A (zh) | 2008-01-09 |
EP1862463A1 (en) | 2007-12-05 |
IL184984A0 (en) | 2007-12-03 |
IL209568A (en) | 2011-11-30 |
JP5027654B2 (ja) | 2012-09-19 |
CN101103024A (zh) | 2008-01-09 |
KR20070112381A (ko) | 2007-11-23 |
CA2596737A1 (en) | 2006-09-28 |
CN101103025B (zh) | 2010-09-08 |
CN101928282A (zh) | 2010-12-29 |
EP1840128A4 (en) | 2009-07-22 |
WO2006101081A1 (ja) | 2006-09-28 |
IL184983A0 (en) | 2007-12-03 |
JPWO2006101081A1 (ja) | 2008-09-04 |
AU2006225700A1 (en) | 2006-09-28 |
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