HK1137739B - Short-acting benzodiazepine salts and their polymorphic forms - Google Patents
Short-acting benzodiazepine salts and their polymorphic forms Download PDFInfo
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Description
the present invention relates to short-acting benzodiazepinesSalts and the use of the salts as medicaments, especially for sedative or hypnotic, anxiolytic, muscle relaxant or anticonvulsant purposes.
European patent No. 1,183,243 describes short-acting benzodiazepines comprising carboxylic ester moietiesAnd inactivated by non-specific tissue esterases. The organ-independent clearance mechanism is predictive of these benzodiazepinesThereby providing a more predictable and reproducible pharmacodynamic profile. The compounds are suitable for therapeutic purposes, including sedative-hypnotic, anxiolytic, muscle relaxant, and anticonvulsant purposes. The compounds are short-acting CNS inhibitors, which can be used for intravenous administration in the following clinical setting: preoperative sedation, anxiolytic and amnesic use in perioperative events; conscious sedation during short-term diagnostic, surgical, or endoscopic procedures; as a component for induction and maintenance of general anesthesia prior to and/or concurrently with administration of other anesthetics or analgesics; ICU sedation.
One of the compounds disclosed in EP 1,183,243 (on page 36 of example Ic-8) is 3- [ (4S) -8-bromo-1-methyl-6- (2-pyridinyl) -4H-imidazo [1, 2-a ]][1，4]Benzodiazepine-4-yl]Methyl propionate, represented by the following general formula (I):
although the free base of formula (I) was stable when stored at 5 ℃, it was observed that the samples stored at 40 ℃/75% relative humidity (open) deliquesced, changed in color to yellow to orange, and showed a significant content reduction relative to the initial content (see example 1 below).
It has now surprisingly been found that the compounds of formula (I) form highly crystalline mono (benzenesulfonic) benzenesulfonate salts which are easily isolated from a range of pharmaceutically acceptable solvents and which exhibit good thermal stability, low hygroscopicity and high water solubility.
According to the present invention, there is provided a benzenesulfonate salt of a compound of the following general formula (I). Preferably, the salt is a crystalline salt. Preferably, the crystalline salt has a 1: 1 ratio of the compound of formula (I): stoichiometry of benzenesulfonate. The preparation and characterization of polymorphs of benzenesulfonate salts are described in the examples below.
According to the present invention there is provided a crystalline polymorph of a besylate salt of a compound of formula (I) (herein denoted as besylate salt form 1) which exhibits an X-ray powder diffraction (XRPD) pattern comprising characteristic peaks at about 7.3, 7.8, 9.4, 12.1, 14.1, 14.4, 14.7 or 15.6 degrees 2 theta.
Preferably, the besylate salt form 1 crystalline polymorph exhibits an XRPD pattern comprising characteristic peaks at approximately 7.3, 7.8, 9.4, 12.1, 14.1, 14.4, 14.7, and 15.6 degrees 2 θ.
More preferably, the besylate salt form 1 crystalline polymorph exhibits an XRPD pattern that is between: characteristic peaks are included at 7.25(10.60), 7.84(72.60), 9.36(12.10), 12.13(32.50), 14.06(48.50), 14.41(74.30), 14.70(50.70), 15.60(26.90) [ angle 2 θ degrees (percentage relative intensity) ].
Preferably, the besylate salt form 1 crystalline polymorph has a Differential Scanning Calorimetry (DSC) onset melting temperature in the range of 187-204 ℃, preferably about 191-192 ℃.
The crystal structure of form 1 resolves at 190K (R factor of 6.3). Form I1: 1 compounds:stoichiometry of benzenesulfonate. Its crystallographically asymmetric unit comprises two separate compound molecules and two molecules of benzenesulfonate. The two separate compound molecules are monomicized on the imidazole ring. The crystal structure has the following single crystal dimensions: 7.6868b＝29.2607c＝12.375690 ° for α, 97.7880 ° for β, 90 ° for γ, and P21The space group of (2). The crystal structure is described in more detail in example 9, and the crystallographic coordinates are given in table 17. Bond lengths and angles for type 1 are given in tables 19 and 20, respectively.
According to the present invention there is provided a besylate salt of a compound of formula (I) which is a crystalline polymorph comprising crystals having the following single crystal sizes: 7.6868b＝29.2607c＝12.3756α＝90°，β＝97.7880°，γ＝90°。
According to the present invention there is also provided a besylate salt of a compound of formula (I) which is a crystalline polymorph having a crystal structure defined by the structure coordinates shown in table 17.
There is further provided according to the present invention a benzenesulfonate salt of a compound of the general formula (I), which has bond lengths and angles as shown in tables 19 and 20, respectively.
There is further provided according to the invention a crystalline polymorph of a besylate salt of a compound of formula (I) (herein denoted as besylate salt form 2) which exhibits an XRPD pattern comprising characteristic peaks at about 8.6, 10.5, 12.0, 13.1, 14.4 or 15.9 degrees 2 theta.
Preferably, the besylate salt form 2 crystalline polymorph exhibits an XRPD pattern comprising characteristic peaks at approximately 8.6, 10.5, 12.0, 13.1, 14.4, and 15.9 degrees 2 Θ.
More preferably, the besylate form 2 crystalline polymorph exhibits an XRPD pattern that is between: characteristic peaks are included at 8.64(17.60), 10.46(21.00), 12.03(22.80), 13.14(27.70), 14.42(11.20), 15.91(100.00) [ angle 2 θ degrees (percentage relative intensity) ].
Preferably, the besylate salt form 2 crystalline polymorph has a Differential Scanning Calorimetry (DSC) onset melting temperature in the range of 170-200 ℃, preferably at about 180 ℃.
The crystal structure of form 2 resolves at 190K (R factor of 3.8). Type 2 compounds having a 1: 1 ratio: stoichiometry of benzenesulfonate. Its crystallographically asymmetric unit comprises one compound molecule and one benzenesulfonate molecule. The compound molecule is not protonated on the imidazole ring. The crystal structure has the following single crystal size a ═ 8.92130b＝11.1536c＝25.834590 ° for α, 90 ° for β, 90 ° for γ and P212121The space group of (2). The crystal structure is described in more detail in example 10, and the crystallographic coordinates are given in table 18. The bond lengths and angles for type 2 are given in tables 21 and 22, respectively.
According to the present invention there is provided a besylate salt of a compound of formula (I) which is a crystalline polymorph, which crystalline polymorph isThe form comprises crystals having the following single crystal sizes: 8.92130b＝11.1536c＝25.8345α＝90°，β＝90°，γ＝90°。
According to the present invention there is also provided a besylate salt of a compound of formula (I) which is a crystalline polymorph having a crystal structure defined by the structure coordinates shown in table 18.
There is further provided according to the present invention a benzenesulfonate salt of a compound of the general formula (I), which has bond lengths and angles as shown in tables 21 and 22, respectively.
There is further provided according to the invention a crystalline polymorph of a besylate salt of a compound of formula (I) (herein denoted as besylate salt form 3) which exhibits an X-ray powder diffraction (XRPD) pattern comprising characteristic peaks at about 7.6, 11.2, 12.4, 14.6, 15.2, 16.4 or 17.7 degrees 2 theta.
Preferably, the besylate salt form 3 crystalline polymorph exhibits a crystalline polymorph form at about: XRPD patterns including characteristic peaks at 7.6, 11.2, 12.4, 14.6, 15.2, 16.4, and 17.7 degrees 2 theta.
More preferably, the besylate form 3 crystalline polymorph exhibits an XRPD pattern that is between: characteristic peaks are included at 7.61(65.70), 11.19(33.20), 12.38(48.70), 14.63(30.60), 15.18(33.20), 16.40(29.60), 17.68(51.30) [ angle 2 θ ° (percentage relative intensity) ].
Preferably, the besylate salt form 3 crystalline polymorph has a Differential Scanning Calorimetry (DSC) onset melting temperature in the range of 195-205 deg.C, preferably about 200-201 deg.C.
There is further provided according to the invention a crystalline polymorph of a besylate salt of a compound of formula (I) (herein denoted as besylate salt form 4) which exhibits an XRPD pattern comprising characteristic peaks at about 7.6, 10.8, 15.2, 15.9 or 22.0 degrees 2 theta.
Preferably, the crystalline polymorph of besylate salt form 4 exhibits a crystal morphology in the approximate range of: XRPD patterns including characteristic peaks at 7.6, 10.8, 15.2, 15.9, and 22.0 degrees 2 theta.
Preferably, the besylate salt form 4 crystalline polymorph exhibits an XRPD pattern that is between: characteristic peaks are included at 7.62(83.50), 10.75(14.70), 15.17(37.80), 15.85(28.70), 22.03(100) [ angle 2 θ ° (percentage relative intensity) ].
Preferably, the besylate salt form 4 crystalline polymorph has a Differential Scanning Calorimetry (DSC) onset melting temperature in the range of 180-185 ℃, preferably at about 182 ℃.
The preferred salt is besylate form 1 based on the robustness, yield, purity and chemical and solid shape stability of the formation.
According to the present invention there is also provided a process for the manufacture of a benzenesulphonic acid salt of a compound of formula (I), which process comprises reacting the free base of the compound of formula (I) with benzenesulphonic acid.
According to the invention there is also provided a process for the manufacture of a salt of the invention, which process comprises contacting the free base of a compound of formula (I) with benzenesulphonic acid in solution to cause the formation of a precipitate of the benzenesulphonic acid salt. Preferably, the method further comprises isolating the precipitate.
Preferably, the free base is dissolved in toluene, ethanol, ethyl acetate, MtBE, Dichloromethane (DCM), isopropyl acetate, ethyl formate, methanol or acetone. More preferably, the free base is dissolved in toluene or ethyl acetate. Preferably, the benzenesulfonic acid is dissolved in ethanol.
Besylate form 1 can be prepared as follows: a solution of the free base of the compound of formula (I) in toluene, ethyl acetate, acetone, isopropyl acetate or ethyl formate is contacted with a solution of benzenesulfonic acid in ethanol to cause the formation of a precipitate of the salt.
According to the present invention there is also provided a benzenesulphonic acid salt of a compound of general formula (I) obtainable by the above process.
Besylate form 2 can be prepared as follows: a solution of the free base of the compound of formula (I) in methanol is contacted with a solution of benzenesulfonic acid in ethanol to cause the formation of a precipitate of the salt. Preferably, the mixture is cooled to less than ambient temperature (e.g., 4 ℃).
According to the present invention there is also provided a benzenesulphonic acid salt of a compound of general formula (I) obtainable by the above process.
Besylate form 3 can be prepared as follows: seeding with a body fluid in which form 1 is produced from crystallization of form 1 from ethyl acetate/ethanol. Preferably, the liquid is cooled to less than ambient temperature (e.g., 4 ℃).
In one embodiment, benzenesulfonate form 3 may be prepared as follows: seeding a filtrate, which is separated from a precipitate formed by contacting a solution of the compound of formula (I) in ethyl acetate with a solution of benzenesulfonic acid in ethanol, with the besylate salt of formula (I) form 1 crystalline salt to produce besylate salt form 3 crystalline polymorph.
According to the present invention there is also provided a benzenesulphonic acid salt of a compound of the general formula (I) obtainable by any one of the above processes.
Besylate form 4 can be prepared by recrystallizing besylate form 1 from isopropyl acetate/ethanol, preferably 40% isopropyl acetate/ethanol.
According to the present invention there is also provided a benzenesulphonic acid salt of a compound of general formula (I) obtainable by the above process.
The salts of the invention may also be prepared as follows: crystallizing the benzenesulfonate salt of the compound of formula (I) from a suitable solvent, or from a suitable solvent/anti-solvent or solvent/co-solvent mixture. If appropriate, the solution or mixture can be cooled and/or evaporated to effect crystallization.
It has been found that crystallization of form 2 is observed under extreme conditions in which polar (e.g. acetonitrile: water) or lipophilic (n-nonane) or both (dimethylsulfoxide: 1, 2-dichlorobenzene) are present.
Examples of solvents for type 2 crystallization are: nonane; methanol.
Examples of solvent/anti-solvent mixtures for type 1 crystallization are: dimethylacetamide/methyl isobutyl ketone; dimethylacetamide/tetrachloroethylene; acetonitrile/3-methylbutan-1-ol; acetonitrile/1, 2-dichlorobenzene; acetonitrile/amyl acetate; methanol/3-methylbutan-1-ol; methanol/methyl isobutyl ketone; 2, 2, 2-trifluoroethanol/1, 4-xylene; ethanol/methyl isobutyl ketone; ethanol/1, 4-xylene; propan-1-ol/1, 2-dichlorobenzene; propan-1-ol/tetrachloroethylene; propan-2-ol/1, 2-dichlorobenzene; propan-2-ol/n-nonane; 2-methoxyethanol/water; 2-methoxyethanol/amyl acetate; 2-methoxyethanol/1, 4-xylene; tetrahydrofuran/water; tetrahydrofuran/3-methylbutan-1-ol; tetrahydrofuran/1, 2-dichlorobenzene; tetrahydrofuran/ethyl acetate; tetrahydrofuran/1, 3-xylene.
Examples of solvent/anti-solvent mixtures for type 2 crystallization are: ethanol/ethyl acetate; ethanol/methyl isobutyl ketone; ethanol/p-isopropylbenzene; dimethyl sulfoxide/1, 2-dichlorobenzene; acetonitrile/water; ethanol/1, 2-dichlorobenzene; ethanol/tetrachloroethylene; tetrahydrofuran/1, 2-dichlorobenzene; tetrahydrofuran/ethyl acetate.
According to a preferred embodiment, form 1 is crystallized from 2-methoxyethanol/amyl acetate.
According to a preferred embodiment, form 2 is crystallized from ethanol/ethyl acetate.
According to a preferred embodiment, form 2 is crystallized from methanol/ethanol (preferably by cooling a solution of the besylate salt of the compound of formula (I) in methanol/ethanol to less than ambient temperature, e.g. 4 ℃).
According to a preferred embodiment, form 3 is crystallized from ethanol/ethyl acetate (suitably by cooling the mixture to less than ambient temperature, e.g. 4 ℃).
According to a preferred embodiment, form 4 is crystallized from isopropyl acetate/ethanol (preferably by cooling a solution of the besylate of the compound of formula (I) in isopropyl acetate/ethanol to ambient temperature).
According to the present invention there is also provided a benzenesulphonic acid salt of a compound of the general formula (I) obtainable by any one of the above processes.
The preparation method of the salt of the present invention will be described in detail in the following examples.
The salts of the invention may be used as medicaments, in particular for sedative or hypnotic, anxiolytic, muscle relaxant or anticonvulsant purposes.
Although administration of the salts of the present invention as bulk active chemicals is possible, it is preferred that they be provided with pharmaceutically acceptable carriers, excipients or diluents to form pharmaceutical compositions. The carrier, excipient or diluent must, of course, be compatible to some extent with the other ingredients of the composition and not deleterious to the recipient thereof.
Accordingly, the present invention provides a pharmaceutical composition comprising a salt of the invention and a pharmaceutically acceptable carrier, excipient or diluent.
The pharmaceutical compositions of the present invention include those suitable for oral, rectal, topical, buccal (e.g., sublingual) and parenteral (e.g., subcutaneous, intramuscular, intradermal or intravenous) administration.
Preferably, the salts of the present invention are provided in the form of pharmaceutical compositions for parenteral administration (e.g., by intravenous or intramuscular injection of a solution). When the pharmaceutical composition is for parenteral administration, the composition may be an aqueous or non-aqueous solution or a mixture of liquids, which may include bacteriostats, antioxidants, buffers or other pharmaceutically acceptable additives.
Preferred formulations of the salts of the invention are in aqueous acidic media at pH 2-4 or in aqueous solutions of Cyclodextrins (CD). Cyclodextrins that may be used in these formulations are the anionic charged sulfobutyl ether (SBE) derivatives of beta-CD, particularly SBE 7-beta-CD, sold under the trade name Captisol by CyDex, Inc. (Critical Reviews in Therapeutic drug Carrier Systems, 14(1), 1-104(1997)), or hydroxypropyl CD's.
Another preferred formulation of the salt of the invention is a lyophilized formulation which comprises, in addition to the salt, at least one of the following reagents: ascorbic acid, citric acid, maleic acid, phosphoric acid, glycine hydrochloride, succinic acid or tartaric acid. These agents are believed to act as buffering, clumping or contrast agents. In some cases, it may be beneficial to include sodium chloride, mannitol, polyvinylpyrrolidone, or other ingredients in the formulation.
The preferred method of formulation (i.e., acid buffer or CD base) may depend on the physicochemical properties (e.g., water solubility, pKa, etc.) of the particular salt. Preferably the salt may also be present as a lyophilized solid for reconstitution with water (for injection) or dextrose or saline solution. Such formulations are typically presented in unit dosage forms such as ampoules or disposable syringes. They may also be presented in multi-dose dosage forms, such as bottles from which appropriate doses may be taken. All of these formulations should be sterile.
According to the present invention there is provided a method of producing a sedative or hypnotic state in a subject, the method comprising administering to the subject a sedatively or hypnotically effective amount of a salt of the invention.
There is also provided according to the invention a method of inducing anxiolytic activity in a subject, the method comprising administering to the subject an anxiolytic effective amount of a salt of the invention.
There is further provided according to the invention a method of inducing muscle relaxation in a subject, the method comprising administering to the subject a muscle relaxing effective amount of a salt of the invention.
Further provided according to the invention is a method of treating a convulsive state in a subject, the method comprising administering to the subject an anticonvulsant effective amount of a salt of the invention.
There is also provided according to the invention the use of a sedative or hypnotic amount of a salt of the invention in the manufacture of a medicament for use in the production of a sedative or hypnotic state in a subject.
Also provided according to the invention are salts of the invention for use in producing a sedative or hypnotic state in a subject.
There is also provided according to the invention the use of an anxiolytic amount of a salt of the invention in the manufacture of a medicament for use in the production of an anxiolytic state in a subject.
There is also provided according to the invention a salt of the invention for use in the production of an anxiolytic state in a subject.
There is further provided according to the invention use of a muscle relaxing amount of a salt of the invention in the manufacture of a medicament for use in producing a muscle relaxed state in a subject.
There is further provided according to the invention a salt of the invention for use in producing a muscle relaxation state in a subject.
Further provided according to the invention is the use of an anticonvulsant amount of a salt of the invention in the manufacture of a medicament for treating a convulsive state in a subject.
Further provided according to the invention is a salt of the invention for use in the treatment of convulsive states in a subject.
The subject is suitably a mammal, preferably a human.
Suitable pharmaceutical parenteral formulations for administration to humans will preferably contain 0.1 to 20mg/ml of a salt of the invention in solution or multiples thereof for multi-dose vials.
Intravenous administration may take the form of bolus injection or, more suitably, continuous infusion. The dosage for each subject may vary, however, a suitable intravenous amount or dosage of a salt of the invention to achieve a sedated or hypnotic state in a mammal will be 0.01-5.0mg/kg body weight, more particularly 0.02-0.5mg/kg body weight, based on the weight of the salt which is the active ingredient. Suitable intravenous amounts or dosages of the salts of the invention to achieve an anxiolytic state in a mammal will be 0.01-5.0mg/kg body weight, more particularly 0.02-0.5mg/kg body weight, based on the weight of the salt which is the active ingredient. Suitable intravenous amounts or dosages of the salts of the invention to achieve muscle relaxation in a mammal will be from 0.01 to 5.0mg/kg body weight, more especially from 0.02 to 0.5mg/kg body weight, based on the weight of the salt which is the active ingredient. Suitable intravenous amounts or dosages of the salts of the invention for the treatment of convulsive states in mammals will be from 0.01 to 5.0mg/kg body weight, more especially from 0.02 to 0.5mg/kg body weight, based on the weight of the salt being the active ingredient.
The salts of the present invention are short-acting CNS inhibitors, which can be used for intravenous administration in the following clinical settings: preoperative sedation, anxiolytic and amnesic use in perioperative events; conscious sedation during short-term diagnostic, surgical, or endoscopic procedures; as a component for induction and maintenance of general anesthesia prior to and/or concurrently with administration of other anesthetics or analgesics; ICU sedation.
Preferred embodiments of the present invention will be described in the following examples with reference to the accompanying drawings, in which:
FIG. 1 shows a graph of the content (% relative to the initial) of the compound of formula (I) versus the storage temperature;
FIG. 2 shows Differential Scanning Calorimetry (DSC) of LJC-039-;
FIG. 3 shows a DSC of LJC-039-;
figure 4 shows DSC of besylate crystalline form (solid line form 1, hatched line form 2);
figure 5 shows DSC of besylate crystalline form (solid, dashed and hatched form 1);
FIG. 6 shows LJC-039-037-1 at T0And T4Chromatography (and to the results in table 10);
FIG. 7 shows an XRPD comparing LJC-039-037-1 (benzenesulfonate salt) before and after a 4-week stability study;
figure 8A shows an XRPD comparison of besylate forms 1 and 2;
figure 8B shows Differential Scanning Calorimetry (DSC) coverage for forms 1 and 2;
figure 9A shows an XRPD comparison of besylate forms 1 and 3, and figure 9B shows an overlay of forms 1 and 3;
FIG. 10 shows DSC of LJC-039-086-1 (benzenesulfonate salt type 4);
figure 11 shows the results for benzenesulfonate form 1: A) XRPD of 100mg batches LJC-039-037-1; B)100mg batch of LJC-039-037-1 DSC; C) TGA of 100mg batches LJC-039-; D) 1H NMR for 100mg batches LJC-039-037-1; E)100mg batch GVS of LJC-039-037-1; F) XRPD after GVS of 100mg batch LJC-039-037-1; G) XRPD after stabilization of 100mg batches LJC-039-1 at 40 ℃/75% RH; H) VT of 100mg batch LJC-039-037-1; I) light polarization microscopy of 100mg batches LJC-039-;
figure 12 shows the results for benzenesulfonate form 2: A) XRPD of 100mg batches LJC-039-; B)100mg batch LJC-039-067-8 DSC; C) DSC at a temperature change rate of 2 ℃/min; D) LJC-039-067-8 of1H NMR；
Figure 13 shows the results for benzenesulfonate form 3: A) XRPD of LJC-039-; B) DSC of LJC-039-; C) DSC of LJC-039-; D) TGA of LJC-039-; E) LJC-039-081-21H NMR; F) GVS of LJC-039-; G) XRPD of LJC-039-;
figure 14 shows the results for benzenesulfonate form 4: A) XRPD of LJC-039-086-1; B) DSC of LJC-039-086-1; C) of LJC-039-086-11H NMR；
FIG. 15 shows an HPLC chromatogram of a release batch of benzenesulfonate salt, followed by AgilentChemStation reporting detailed results;
FIG. 16 shows chiral chromatograms of LJC-039-;
figure 17 shows an exemplary image of a solid crystalline form observed in the crystallization of the compound benzenesulfonic acid of formula (I) (approximately 4-8mm diameter field);
FIG. 18 shows the content of asymmetric units in type 1;
FIG. 19 shows the molecular structure determined by single crystal X-ray diffraction of a crystal of benzenesulfonate salt (form 1) of a compound of the general formula (I) grown from a 2-methoxyethanol amyl acetate solution having atoms represented by thermal ellipsoids. Only the hydrogen specifically located in the crystal structure is depicted;
FIG. 20 shows the conformation adopted by two independent molecules in type 1;
FIG. 21 shows a comparison of the conformation adopted by one independent molecule in type 1 (top) and the conformation in type 2 (bottom);
figure 22 shows a comparison of the conformations adopted by two independent benzenesulfonates in form 1, viewed in two different directions;
figure 23 shows a comparison of the conformation adopted by one of the independent benzenesulfonates in form 1 (top) and the conformation in form 2 (bottom);
FIG. 24 shows a crystal structure determined by single crystal X-ray diffraction of a crystal of benzenesulfonic acid compound of formula (I) grown from a 2-methoxyethanol: amyl acetate solution, observed along crystallographic a-axis (a), b-axis (b), and c-axis (c);
FIG. 25 shows short contact C-O < 3.6 for type 1C-C＜3.6And N-O < 3.5
FIG. 26 shows a powder diffraction pattern calculated from single crystal X-ray diffraction data for type 1;
FIG. 27 shows plate-shaped crystals observed for benzenesulfonate salt form 2 of the compound of the formula (I);
FIG. 28 shows the content of asymmetric units in type 2;
fig. 29 shows the molecular structure determined by single crystal X-ray diffraction of a crystal of the benzenesulfonate salt form 2 of the compound of the general formula (I), which crystal has atoms represented by thermal ellipsoids. Only the hydrogen specifically located in the crystal structure is depicted;
figure 30 shows the conformation adopted by the individual molecules in form 2;
figure 31 shows the conformations adopted by the independent benzenesulfonates in form 2, viewed in two different directions;
fig. 32 shows a crystal structure determined by single crystal X-ray diffraction of a crystal of the compound benzenesulfonate salt 2 form of the general formula (I) observed along crystallographic a-axis (a), b-axis (b), and c-axis (c);
FIG. 33 shows short contact C-O < 3.6 for type 2C-C＜3.6And N-O < 3.5
FIG. 34 shows a powder diffraction pattern calculated from single crystal X-ray diffraction data for form 2;
FIG. 35 shows the labeling of the atomic center of the benzenesulfonate salt type 1 of the compound of the general formula (I); and
FIG. 36 shows the labeling of the atomic center of the benzenesulfonate salt type 2 of the compound of the general formula (I).
Example 1
Solid state stability Studies of Compounds of formula (I)
Methods/techniques. An accurately weighed amount of 2mg of the compound of formula (I) was placed in a 4-mL clear glass screw vial. The samples were tested initially and after 34 days of storage under 5 ℃/ambient relative humidity (AMRH) seal, 30 ℃/60% RH seal, 40 ℃/75% RH open and 60 ℃/AMRH seal.
The appearance of the samples was visually inspected. The values of the content of the compounds of general formula (I) were determined by the HPLC method in table 1. The% weight/weight (% w/w) values are measured relative to a standard sample of compound batch U12438/79/1 of formula (I). The% area value is obtained by dividing the peak area of the compound of formula (I) by the total peak area.
TABLE 1 HPLC method conditions
Results
Appearance. The appearance results are listed in table 2.
TABLE 2 summary of appearance data for the compounds of the formula (I)
| Storage conditions | Point in time | Appearance of the product |
| Sky | ||
| RT | Initially, the process is started | Cream to light yellow powder |
| 5C/AMRH blocking | 34 | Cream to light yellow powder |
| 30C/60% RH blocking | 34 | Cream to light yellow powder |
| 40C/75% RH patency | 34 | Deliquescent yellow substance on the bottom of the vial |
| 60C/AMRH sealing | 34 | Deliquescent dark yellow to orange substances on the bottom of the vial |
The content (% w/w) of the compound of the formula (I). The% w/w content values (see table 3) show too much variability to detect differences between the initial values and those measured after 5 ℃/AMRH block, 30 ℃/60% RH block or 40 ℃/75% RH open set-down for 34 days. The average% w/w measured for samples stored for 34 days at 60 ℃/AMRH closure showed a 10% w/w reduction from the initial value.
The content (% by area) of the compound of the formula (I). The% area content of the compound of formula (I) (see table 3 and figure 1) showed no significant change after 34 days of storage at 5 ℃/AMRH block, but steadily decreased with increasing storage temperature of the sample at 30 ℃/60% RH block, 40 ℃/75% RH open or 60 ℃/AMRH block. Major tapering peaks were observed at RRT 0.68, 0.87 and RRT0.90, but the chromatograms, which were more complex even initially (23 peaks), also showed many new small tapering peaks (e.g., 7 peaks at 30 ℃/60% RH closure; 13-20 peaks at 60 ℃/AMRH closure). These observations suggest multiple decreasing paths. The decrease at RRT 0.68 was tentatively determined as the ester hydrolysate (free acid of the compound of formula (I)). It is most prevalent in open samples at 40 ℃/75% RH, as would be expected for hydrolysates.
TABLE 3 summary of HPLC data for compounds of formula (I)
Footnote
1. Only one sample was tested due to autosampler sequencer error.
Conclusion
The compounds of formula (I) are stable in appearance and content for at least 34 days of storage under a 5 ℃/AMRH seal. No change in appearance was seen at 30 ℃/60% RH blocking, but an approximately 0.6% reduction in the level of compound of formula (I) relative to the initial% area was observed. Samples stored at 40 ℃/75% RH open or 60 ℃/AMRH closed deliquesced, turning yellow to orange in color and showed a significant reduction (1.5-8%) in the content of the compound of formula (I) relative to the initial. Major degressive peaks at RRT 0.68, 0.87 and RRT0.90 are observed, as well as many smaller peaks, suggesting multiple degressive paths. The decreasing peak at RRT 0.68 was experimentally determined to be the ester hydrolysate. These results indicate that the compounds of formula (I) should be stored frozen for long term storage.
Example 2
The solubility of the compounds of the general formula (I) is determined in a wide range of organic solvents. The solubility data is shown in table 4 below.
TABLE 4
| Solvent(s) | Minimum solvent required/mg/ml |
| Methanol | 446 |
| Ethanol | 324 |
| Propan-2-ol | 454 |
| Acetone (II) | 214 |
| Toluene | 460 |
| Ethyl acetate | 218 |
| Tetrahydrofuran (THF) | 311 |
| Acetonitrile | 362 |
The data clearly show that the compounds of formula (I) have high solubility in common organic solvents. Preferred solvents are ethanol and toluene.
The pKa of the free base of this compound was measured for both basic centers. However, the basic center of the pyridine ring has a pKa of 1.99. The pKa of the basic center of the imidazole ring was found to be 4.53.
The benzenesulfonate salt of the compound of formula (I) is prepared using benzenesulfonic acid. Experiments were performed on a 20mg scale using 6 volumes of solvent. All reactions were carried out at ambient temperature with acid added as a raw material solution in ethanol (1M) or as a solid (depending on solubility).
Isolated solids in1Significant peak shifts were shown in H NMR to confirm salt formation. X-ray powder diffraction (XRPD) showed that the salt had a crystalline indication. Table 5 summarizes the isolated salt crystal forms.
TABLE 5
| Item | Salt (salt) | Solvent(s) | ID |
| 1 | Benzenesulfonic acid salt | Toluene | LJC-039-009-7 |
The salt was then stored at 40 ℃/75% RH for two weeks and then re-analyzed for chemical purity by XRPD and HPLC to assess the stability of the material. The salt maintains the same powder pattern after exposure to the humidity conditions, and furthermore maintains a high chemical purity, supporting improved stability.
Isolation of T from the salt1Purity results (table 6 below) it can be seen that the benzene sulfonate salt from toluene showed high purity values before and after the stability study.
TABLE 6 summary of purity before and after 1 week of 40 ℃/75% RH hold
| Item | Salt (salt) | ID | Purity T0/％ | Purity T1/％ |
| 1 | Benzenesulfonic acid salt | LJC-039-009-7 | 95.9 | 95.9 |
The above results indicate that the besylate salt crystalline form exhibits high purity and favorable stability results.
Example 3
The besylate salt was scaled up to 100mg based on the data in example 2. Toluene was found to be the preferred solvent for isolation of the benzenesulfonate salt.
Benzenesulfonate of a compound of the general formula (I)
The feed was scaled up to 50mg in order to confirm whether the process was scaled up and whether the isolated material had the same crystalline morphology (form 1) as seen in the previous small scale experiment. Once the analysis confirmed that the salt was form 1 and the properties were consistent with those expected, a further scale-up was performed with 100mg feed for complete characterization and the sample was used for a 4-week stability study at 40 ℃/75% RH. These two scale-up reactions were carried out in toluene, with benzenesulfonic acid added as a solution (1M) in ethanol.
Besylate salt Experimental procedure
The free base of the compound of formula (I) (100mg, batches 704-17) was added to a vial and toluene (600. mu.l) was added at ambient temperature. To the solution was added benzenesulfonic acid (250 μ l, 1M in ethanol) and the reaction mixture was stirred for fifteen minutes, after which the solid precipitated from the solution was filtered, washed with toluene and dried under vacuum at 40 ℃. Analysis by XRPD showed that the solid had the same powder pattern as the other benzenesulfonates produced, and1HNMR demonstrated that salts were formed due to significant peak shifts.
TABLE 7
| Item | ID | Salt (salt) | GVS uptake/%) | Initial melt/. degree.C | TGA weight loss/%) | Solubility mg/ml | Chemical purity/%) | Chiral purity/% e.e |
| 1 | LJC-039-037-1 | Benzenesulfonic acid salt | 2.0 | 201.3 | 4.9 | 8.3 | 97.1 | 94.4 |
The enantiomeric excess of LJC-039-. The enantiomeric excess of this batch was 99.1%.
Method optimization
To improve the yield of further benzenesulfonate (form 1), four solvents (isopropyl acetate, ethyl formate, methanol and acetone) were screened. A total of eight 100mg scale reactions were carried out in these solvents with the relevant acids added as starting solutions in ethanol for comparison with the previous experiments.
The compounds of formula (I) (batches 704-38, 100mg) were dissolved in a solvent (600. mu.l) at ambient conditions. Acid (250 μ l, 1M stock solution in ethanol) was added and the whole reaction mixture was allowed to stand at ambient for 48 hours. The results are summarized in table 8.
TABLE 8 results of the optimization experiment
| Table item | Laboratory workbook reference | Salt (salt) | Solvent(s) | XRPD | Yield/%) | Purity/% area | Purity after 4 weeks hold at 40 ℃/75% RH |
| 1 | LJC-039-067-2 | Benzenesulfonic acid salt | Acetone (II) | Type 1 | 38 | 98.4 | 98.1 |
| 2 | LJC-039-067-4 | Benzenesulfonic acid salt | Acetic acid isopropyl ester | Type 1 | 79 | 97.7 | 95.9 |
| 3 | LJC-039-067-6 | Benzenesulfonic acid salt | Formic acid ethyl ester | Type 1 | 40 | 98.6 | 98.3 |
| 4 | LJC-039-067-8 | Benzenesulfonic acid salt | Methanol | Single crystal, type 2 | Has no record | 98.1 | Has no record |
All reactions except the benzene sulfonate formation in methanol show form 1. The methanol reactant was stored at 4 ℃. The data obtained confirmed the anhydrous benzenesulfonate salt 1: 1, and the powder pattern of the material confirmed the presence of the new crystalline form (form 2).
From this study it was concluded that solvents such as isopropyl acetate increased the purity of the salt, however, reduced the recovery. Since the aforementioned selection of solvent (ethyl acetate) resulted in a high yield of salt with high purity values, it was decided to use ethyl acetate for the final scale-up experiment.
Scale Up of 1g of benzenesulfonate (type 1)
1g of benzenesulfonate was formed. This successfully produced 950mg (70% yield) of form 1. The solution was highly colored (yellow) and therefore seeded with a small amount of type 1 to aid in recovery. The solution was stored at 4 ℃ for 16 hours. The obtained solid showed a new powder pattern (type 3). The solid was analyzed by thermal analysis and variable temperature XRPD to confirm whether it was the actual polymorph or solvate. Interpretation of the analysis concludes according to1H NMR case demonstrates that it is not a solvate, and DSC shows two endothermic events confirmed by high temperature microscopy (figure 3). It is explained that seeds of type 1 melt at 187 ℃ and type 3 at 200 ℃. The reason that form 1 was not identified by XRPD is that it is a less sensitive technique than microscopy.
Form 3 precipitates to form 1 at lower temperatures.
The polymorphs were characterized to suggest the relationship between them.
Table 9 thermal data for besylate salt crystal form
| Item | ID | Crystal form | Onset of melting/. degree.C | ΔH/Jg-1 |
| 1 | LJC-039-081-1 | 1 | 201 | 56 |
| 2 | LJC-039-067-8 | 2 | 180 | 73 |
| 3 | LJC-039-081-2 | 1，3 | 187，200 | 7.6，37 |
The lower melting point of the small amount of type 1 present in LJC-039-081-2 may be attributed to the lower purity (97.2% compared to 97.9% in LJC-039-081-1).
Figure 4 shows the DSC of besylate forms 1 (solid line) and 2 (hatched line).
Figure 5 shows DSCs for besylate forms 1 (solid line) and 3 (dashed and hatched).
Example 4
Study of salt stability
TABLE 10 summary of salt purity after 4 weeks stability study
| Sample ID | Salt (salt) | T0 | T1 | T2 | T3 | T4 |
| LJC-039-037-1 | Benzenesulfonic acid salt | 97.1 | 97.3 | 97.4 | 96.7 | 96.7 |
The crystalline sample of benzenesulfonate was stored at 40 ℃/75% RH for a total of four weeks and the sample was pipetted for HPLC every seven days. The benzene sulfonate hplc purity remained consistent until T3At this point it reaches 96.7%. However, this value remains with T4And (5) the consistency is achieved.
Hplc chromatograms of the besylate salt form at time points zero and four weeks are shown in figure 6.
It is suspected that the main peak preceding the parent peak is from contamination, since λ max does not match λ max of the parent peak. T is1、T2、T3And T4Nor in the impurity profile of (c).
As can be seen from the powder patterns of the salt before and after the wetting study, there was no change in the crystal form.
FIG. 7 shows an XRPD comparing LJC-039-037-1 (benzenesulfonate) before and after a 4-week stability study.
Example 5
Polymorphism study
To determine the propensity of the benzenesulfonate salt to exhibit polymorphism, a mature experiment was set up using thirty solvents (fifteen pure plus their 2.5% aqueous counterparts). The solids were slurried in various solvents (see table 11) for one week based on a heating/cooling cycle from ambient to 60 ℃. After one week, the slurry was evaporated and the solids were analyzed by XRPD and HPLC.
TABLE 11 results of the study on the polymorphism of benzenesulfonate salt (LJC-039-058-2)
Initial hplc purity 97.7%
| Item | Solvent(s) | XRPD after 1 week | HPLC purity% area |
| 1 | Acetone (II) | Type 1 | 97.5 |
| 2 | THF | Type 1 | 97.6 |
| 3 | IPA | Powder of | 97.1 |
| 4 | MtBE | Type 1 | 97.7 |
| 5 | DCM | Powder of | 97.4 |
| 6 | EtOH | Oil | Without analysis |
| 7 | MEK | Type 1 | 97.2 |
| 8 | 1, 4-dioxane | Type 1 | 97.2 |
| 9 | iPrOAc | Type 1 | 97.5 |
| 10 | DMF | Oil | Without analysis |
| 11 | MeCN | Type 1 | 94.3 |
| 12 | nBuOH | Oil | Without analysis |
| 13 | nPrOH | Oil | Without analysis |
| 14 | MIBK | Type 1 | 97.7 |
| 15 | MeOH | Oil | Without analysis |
| 16 | 2.5% aqueous acetone solution | Type 1 | 96.8 |
| 17 | 2.5% aqueous THF solution | Powder of | 93.3 |
| 18 | 2.5% aqueous IPA solution | Type 1 | 76.1 |
| 19 | 2.5% MtBE in water | Oil | Without analysis |
| 20 | 2.5% aqueous DCM solution | Type 1 | 97.4 |
| 21 | 2.5% EtOH in water | Oil | Without analysis |
| 22 | 2.5% aqueous MEK solution | Type 1 | 93.9 |
| 23 | 2.5% 1, 4-dioxane aqueous solution | Type 1 | 86 |
| 24 | 2.5% iPrOAc aqueous solution | Oil | Without analysis |
| 25 | 2.5% DMF in water | Oil | Without analysis |
| 26 | 2.5% MeCN in water | Type 1 | 93.3 |
| 27 | 2.5% aqueous nBuOH solution | Oil | Without analysis |
| 28 | 2.5% aqueous nPrOH solution | Oil | Without analysis |
| 29 | 2.5% aqueous MIBK solution | Type 1 | 97.3 |
| 30 | 2.5% aqueous MeOH | Oil | Without analysis |
This maturation study using benzenesulfonate salts revealed no new crystalline forms. The purity results after maturation show that those slurried in acetonitrile, aqueous THF, aqueous IPA, aqueous MEK, aqueous dioxane and aqueous acetonitrile are reduced. This indicates that the benzenesulfonate salt (form 1) has good solution stability at high temperatures in pure organic solvents.
Study of novel crystalline forms of benzenesulfonate
While no new crystalline form of benzenesulfonate was seen from the mature study, a new crystalline form was seen when the crystals were grown in methanol. The single crystal obtained from methanol was ground to obtain a powder pattern. The pattern was found to be different from type 1. Repeat experiments were performed to obtain additional supplies of form 2. It is only possible to isolate form 2 from the solution by precipitation within 16 hours, as opposed to allowing the solvent to evaporate, which results in form 1. There are interestingly two modalities; needles and blocks. Both showed the same powder pattern as the needle morphology used for single crystal structure determination.
The full analysis was performed for type 2. It has been judged to be a true polymorph because the single crystal data confirms the anhydrous benzenesulfonate salt 1: 1.
Figure 8A shows an XRPD comparison of besylate forms 1 and 2. There was a clear difference between type 1 (trace 1) and type 2 (trace 2). From these two powder patterns, it can be seen that the two crystalline forms are very different. Thermal analysis was performed to compare the melting points of the two forms and thermodynamic solubility measurements were also recorded.
Fig. 8B shows an overlay of type 1 and type 2. Forms 1 and 2 show endothermic events (melting).
Type 3 was confirmed when the second harvest was isolated from a solution of LJC-039-. Analysis was performed to determine if it was a solvate and how the crystalline forms were interchanged.
Figure 9A shows an XRPD comparison of besylate forms 1 and 3. Fig. 9B shows an overlay of type 1 and type 3.
Type 1 shows an endothermic event (melting), while type 3 shows two events. High temperature microscopy on type 3 clearly shows two melting points within 20 ℃ of each other. It is postulated that there is a small amount of the lower melting polymorph because it is not obtained in variable temperature XRPD, a less sensitive technique. It is quite possible that the first endotherm represents type 1, as it serves to seed the solution from which type 3 was isolated.
The solubility data indicate that all three forms have very similar aqueous solubilities at pH 3 of 7.8-8.3 mg/ml.
Benzenesulfonate 4 form
The release batch of benzenesulfonate salt form 1 (LJC-039-083-1) is of high purity (97.6%) but contains a small amount of impurities (0.78%, 11.9 min RT) loaded from the free base. This impurity was observed in DSC experiments showing an endothermic transition (starting at 130 ℃). This peak was confirmed to have a max independent of the parent peak.
100mg of sample was taken for recrystallization from 40% isopropyl acetate/ethanol. Recrystallization is conventionally performed by dissolving the salt in a minimum amount of hot solvent, then slowly cooling to the environment to produce a precipitate. The dry solid was analyzed by XRPD, which indicates a new crystalline form, and thermal analysis was used and1h NMR, confirming it is a polymorph and not a solvate. FIG. 10 shows the DSC of LJC-039-086-1.
This salt screening study has shown that the compounds of formula (I) form many salts within the appropriate pKa range and that they are easily isolated from a range of solvents. From a complete characterization of the salt, it has been determined that the benzenesulfonate salt has good stability with respect to humidity. Two polymorphs of benzenesulfonate have been concluded to exist. Type 3 from the second harvest of LJC-039-. Form 4 was observed after recrystallization of form 1 from 40% isopropyl acetate/ethanol.
The overall analytical data is shown in FIGS. 11-14 below.
Experimental methods of examples 2 to 5
Example 2
The compound of formula (I) (5 mg/well) was dissolved in the solvent in the HPLC vial1(30. mu.l). To the solution was added benzenesulfonic acid (11.4 μ l, 1M in ethanol) and the reaction mixture was allowed to stand overnight at ambient. Those vials containing the solids were dried under vacuum at 40 ℃, those remaining as solutions were concentrated by evaporation, and then treated with heptane. The precipitated ones were dried as mentioned, the ones oiled were stored at 4 ℃.
Scaling up besylate form 1
The compound of formula (I) (100mg) was dissolved in ethyl acetate (600. mu.l) and benzenesulfonic acid (250. mu.l, 1M in ethanol) was added. Precipitation occurred immediately and the reaction mixture was stirred at ambient for 24 hours. The solid was filtered, washed with ethyl acetate and dried under vacuum at 40 ℃ for 16 h.
Analytical method
Differential Scanning Calorimetry (DSC)
DSC data was collected on a TA instrument Q1000 equipped with a 50-position autosampler. The energy and temperature calibration standard was indium. The sample was heated at a rate of 10 c/min between 25 and 350 c. A 30 ml/min nitrogen purge was maintained over the sample.
Unless otherwise stated, 0.5-3mg samples were used and all samples were run in a pinhole aluminum pan.
Thermogravimetric analysis (TGA)
TGA data was collected on a TA instrument Q500TGA, calibrated with Alumel and run at a scan rate of 10 ℃/min. A nitrogen purge of 60 ml/min was maintained over the sample.
Unless otherwise stated, typically, 5-10mg of sample was loaded onto a pre-tared platinum crucible.
NMR
All spectra were collected at Bruker 400MHz equipped with an autosampler. Unless otherwise indicated at d6Samples were prepared in DMSO.
XRPD (X-ray powder diffraction)
bruker AXS C2 GADDS diffractometer
X-ray powder diffraction patterns of the samples were obtained on a Bruker AXS C2 GADDS diffractometer using Cu ka radiation (40kV, 40mA), an automatic XYZ stage, a laser disc microscope for automatic sample positioning and a HiStar 2-dimensional area detector. The X-ray optical system consists of a sheet coupled with a 0.3mm pinhole collimatorA multilayer mirror.
The beam divergence, i.e. the effective size, of the X-ray beam on the sample is about 4 mm. A theta-theta continuous scan mode is used in which the sample is at a distance of 20cm from the detector, which results in an effective 2 theta range of 3.2-29.8 deg.. A typical exposure time for the sample will be 120 s.
Samples run at ambient conditions were prepared as flat plate specimens using powder as received without milling. Approximately 1-2mg of the sample was gently pressed onto the slide to obtain a flat surface. Samples run under non-ambient conditions were mounted on silicon wafers with a thermally conductive compound. The sample was then heated to the appropriate temperature at about 20 ℃/minute followed by isothermal hold for about 1 minute before data collection was initiated.
Purity analysis:
chemical process
Purity analysis was performed on HP1100 Agilent:
the method comprises the following steps: gradient, inverse phase
Method duration/min: 34
Column: phenomenex Gemini C185 μm (2.0X 50mm) (protective box Phenomenex Gemini C18 protective box 2X 4mm)
Column temperature/deg.C: 40
Injection/. mu.l: 5
Flow rate ml/min: 0.8
And (3) detection: UV (ultraviolet) light
Wavelength/nm: 255 (bandwidth of 90 nm), 240 (bandwidth of 80 nm), 254 (bandwidth of 8 nm)
Phase A: 2mmol NH4HCO3(with NH)3Adjusting the solution to pH10)
Phase B: acetonitrile
And (3) time table:
| time/minute | ％A | ％B |
| 0 | 90 | 10 |
| 25 | 10 | 90 |
| 28.8 | 10 | 90 |
| 29 | 90 | 10 |
| 34 | 90 | 10 |
Chiral process
Purity analysis was performed on a Gilson HPLC system:
the method comprises the following steps: isoconcentrate, normal phase
Method duration/min: 50
Column: diacel Chrialcel OJ-H (5 μm) 4.6X 250mm (guard box Diacel Chrialcel OJ-H analysis guard box 5 μm 4.0X 10mm)
Column temperature/deg.C: 40
Injection/. mu.l: 10
Flow rate ml/min: 1.0
And (3) detection: UV (ultraviolet) light
Wavelength/nm: 225 (Single wavelength detector)
Phase A: hexane (C)
Phase B: ethanol
And (3) time table:
| time/minute | ％A | ％B |
| 0 | 93 | 7 |
Gravity Vapor Sorption (GVS) study
All samples were analyzed on a Hiden IGASorp moisture sorption analyzer running CFRSorp software. The sample size is typically 10 mg. The moisture sorption desorption isotherms were performed as outlined below (2 scans produced 1 full cycle). All samples were loaded/unloaded at typical room humidity and temperature (40% RH, 25 ℃). All samples were analyzed by XRPD after GVS analysis. Unless otherwise stated, standard isothermal analyses were performed at 25 ℃ in the range of 0-90% RH at 10% RH intervals.
Solubility in water
Solubility was measured as follows: sufficient compound was suspended in 0.25ml of solvent (water) to produce a maximum final concentration of 10mg/ml of the parent free form of the compound. The suspension was allowed to equilibrate at 25 ℃ for 24 hours, then the pH was measured and filtered through glass fiber C96 well plates. The filtrate was then diluted 101 x. Quantitation was performed by HPLC reference at approximately 0.1mg/ml standard in DMSO. Different volumes of standard, diluted and undiluted test substance were injected. The solubility was calculated by integrating the peak areas found at the same residence time as the peak maximum in the standard injection. XRPD is typically examined for phase transitions, hydrate formation, amorphization, crystallization, etc., if sufficient solids are present in the filter plate.
Table:
| time/minute | % phase A | % phase B |
| 0.0 | 95 | 5 |
| 1.0 | 80 | 20 |
| 2.3 | 5 | 95 |
| 3.3 | 5 | 95 |
| 3.5 | 95 | 5 |
| 4.4 | 95 | 5 |
pKa determination
The pka assay was performed on a Sirius GlpKa instrument with a D-PAS attachment. The measurement was carried out by potentiometric titration in a methanol: H2O mixture at 25 ℃. The titration medium is ionic strength adjusted with 0.15 MKCl. The values found in the methanol: H2O mixture were extrapolated to 0% co-solvent via Yasuda-ShedlovSky extrapolation.
High temperature microscopy
High temperature microscopy was studied using a Leica LM/DM polarization microscope coupled with a Mettler-Toledo MTFP82HT hot stage at a temperature range of 25-350 ℃ with a typical heating rate of 10-20 ℃/min. A small amount of sample is dispensed onto the slide to allow the individual particles to separate as well as possible. The sample was observed with an x20 objective lens under normal light or cross-polarized light (coupled with a lambda false color filter).
Chiral purity process
System configuration
A pump: gilson 322 binary pump
A detector: gilson 152UV/Vis
An automatic sampler: gilson 233XL rack + Gilson 402 double syringe pump
Column oven: phenomenex Thermasphere TS-130
Software: gilson Unipoint LC software
Column: daicel Chiralcel OJ-H, 5 μm, 4.6X 250mm
Protection of the column: daicel Chiralcel OJ-H analytical protection kit, 5 μm, 4.6X10mm
HPLC conditions
And (3) a channel A: hexane (93%)
And (3) a channel B: ethanol (7%)
Flow rate: 1.0 ml/min
Wavelength of detector 225nm
Column temperature: 40 deg.C
Operating time: 50.0 minutes
Sample Condition
Approximately 0.2mg of sample was dissolved in the appropriate volume of hexane: ethanol 1: 1v/v to obtain a 0.2mg/ml solution. It was closed and placed on a vortex mixer and held at high speed for-15 seconds. If the solids are retained at this point, the sample vial is then ultrasonically shaken for approximately 10 seconds followed by a further 10-15 seconds on a vortex mixer. 10 μ l was injected onto the HPLC system. After an initial repeated injection of hexane: ethanol 1: 1v/v as a blank sample, the samples were injected in duplicate.
Example 5
Pharmacological test examples
The besylate salt form 1 of the present invention was evaluated for its anesthetic and sedative effects. The benzenesulfonic (benzenesulfonic) acid salt was dissolved in physiological saline to administer the test composition to animals. The test compositions were administered to mice, which were placed in individual plexiglass cages (20X 10 cm). Mice were injected with vehicle or test substance by intravenous route. The duration of the latency to sleep and anesthesia (maximum: 90 minutes after administration of the test substance) was recorded. Anesthesia is indicated by loss of the righting reflex (LRR). The orthoreflex test is performed approximately every 20-30 seconds once the animal appears to be sedated. Once no righting reflex is present, the duration of loss of the righting reflex is measured by testing the recovery of the righting reflex approximately every 20-30 seconds thereafter. Eight mice were studied per group and tested blindly. The results of the study are given in the table below.
Mann-Whitney U test:NS is not significant; p < 0.05; p < 0.01
Fisher's exact test(number of mice with LRR): no indication was not significant;
+＝p＜0.05；++＝p＜0.01
(#): if n < 3, no calculation is made
(##): maximum at 90 minutes post injection
The results in the table above indicate that besylate salt form 1 has a short latency to loss of righting reflex and therefore a short induction time to anaesthesia in animals. In addition, mice recovered rapidly from anesthesia as shown by the short duration of loss of righting reflex. Thus, such compounds may provide rapid induction and recovery from anesthesia.
Example 6
Additional conditions for the crystallization of forms 2, 3 and 4
Additional conditions were tested in order to reproduce the previously reported crystallisations of forms 2, 3 and 4. However, as described below, the reported scale is significantly reduced and thus the process is improved.
Type 2
Dissolve 5mg of the solid in 25. mu.l of ethanol and add 10. mu.l of ethanol; the solution was then refrigerated at 4 ℃ for 3 days.
Type 3
Three variants were tried:
1. dissolve 5mg of the solid in 50. mu.l of ethanol and add 120. mu.l of ethyl acetate; the solution was then refrigerated at 4 ℃ for 3 days.
2. Dissolve 10.1mg of the solid in 300. mu.l of methanol and add 120. mu.l of ethyl acetate; the solution was then refrigerated at 4 ℃ for 3 days.
3. Dissolve 2.5mg of the solid in 50 μ l of ethanol in a silanized vial and add 100 μ l of ethyl acetate; the solution was then refrigerated at 4 ℃ for 3 days.
Type 4
Three variants were tried:
1. add the hot (70 ℃) mixture of isopropyl acetate: ethanol (40%: 60% v/v) to 5mg of the hot solid in 20. mu.l aliquots until the solid dissolves (60. mu.l total solvent mixture); the solution was then allowed to cool slowly to ambient temperature initially in a thermostatic water bath at 70 ℃ over a period of several hours.
2.5mg of the solid was dissolved in 180. mu.l of hot (50 ℃) isopropyl acetate: ethanol (40%: 60% v/v) solvent and the solution was allowed to cool slowly to ambient temperature in a thermostatted water bath (initially at 50 ℃) over a period of several hours.
3. A5 mg portion of the solid was dissolved in 100. mu.l of hot (50 ℃) isopropyl acetate: ethanol (40%: 60% v/v) solvent in a silanized vial and the solution was allowed to cool slowly to ambient temperature over a period of hours in a thermostatic water bath (initially at 50 ℃).
Each crystal produced a solid material with a leaf and plate morphology, with type 4 crystals also producing needle-like material.
Example 7
Characterization of the benzenesulfonate salt of the Compound of the formula (I)
The benzenesulfonate salt of the compound of formula (I) is chiral and is believed to have the following single enantiomeric form, the S enantiomer (consistent with the subsequently determined crystal structure):
the heterocyclic structure comprises a basic nitrogen (pKa of about 5) in the imidazole ring, and a weakly basic nitrogen (pKa of about 2) in the pyridyl ring. The imidazole nitrogen will typically be protonated in aqueous solution in the presence of a strongly acidic benzenesulfonate salt (pKa approximately-0.6), where the pyridyl nitrogen may also be protonated in excess benzenesulfonate salt conditions.
The neutral free base crystalline form (i.e., unprotonated) of this compound is expected to be somewhat lipophilic (loP)Octanol to waterAbout 4.0) and will therefore prefer a somewhat lipophilic environment over an aqueous environment. Furthermore, it is likely to retain a degree of lipophilicity even when monoprotonated (logD)Octanol to waterAbout 2, at pH 3), but the effect of the benzenesulfonate counter ion is likely to improve this trend via its inherent hydrophilicity. For the biprotonated form (logD)Octanol to waterAbout 0.6 at pH0), the degree of lipophilicity is further reduced.
The compound also has an excess of hydrogen bond acceptors and therefore will be suitably compatible with hydrogen bonding solvents. It is therefore expected that the compound will prefer to dissolve in a range of polar organic solvents such as alcohols, especially those that provide a partially lipophilic, hydrogen bonding environment. This has been confirmed by experimental evidence (details of the solvent used are given in example 8):
| solvent(s) | Observed solubility (mg/ml) |
| Carboxamides | 350 |
| Water (W) | 2 |
| Dimethyl sulfoxide | 500 |
| Dimethylacetamide | 200 |
| 1, 2-ethanediol | 60 |
| Dimethyl formamide | 300 |
| Acetonitrile | ＞20 |
| Methanol | 400 |
| 2-Ethoxyethanol | 20 |
| 2, 2, 2-trifluoroethanol | 1000 |
| Ethanol | 100 |
| Acetone (II) | 2 |
| Propan-1-ol | 15 |
| Propan-2-ol | 4.8 |
| 2-methoxy ethanol | 167 |
| Hexafluoropropan-2-ol | ＞700 |
| Methylene dichloride | ＜＜0.3 |
| Tetrahydrofuran (THF) | 2.5 |
| Benzoic acid methyl ester | 2 |
| Ethyl acetate | 0.2 |
| Chloroform | ＜＜0.4 |
| 1, 4-dioxane | 1 |
Soluble (> 5mg/ml), partially soluble (2.5-5mg/ml), partially insoluble (0.5-2.5mg/ml, < 0.5mg/ml).
The values quoted are approximate, but confirmed experimentally.
These results emphasize the good solubility of the compound in various polar organic solvents. Specifically, 2, 2, 2-trifluoroethanol and hexafluoropropan-2-ol were identified as extremely good solvents for this compound. This is consistent with the considerations discussed above, the two solvents being strong hydrogen bond donors. Likewise, the more significantly lipophilic solvents are identified as poor solvents and are therefore possible anti-solvents for crystallization.
Example 8
Crystals of benzenesulfonate salt of a compound of the general formula (I)
Various conditions are described which help to obtain crystalline materials of the compound benzenesulfonate forms 1 and 2 of the general formula (I). Crystallization conditions that include an alcohol or acetonitrile solvent as a component with their respective compatible anti-or co-solvents are believed to provide the most promising conditions to produce useful crystalline materials. Crystallization using a binary solvent/anti-solvent mixture is mainly used. Crystallization was performed by delayed evaporation from a sub-saturated solution of the compound in a solvent/anti-solvent mixture at ambient temperature and reduced (4 ℃). Crystallization is usually observed within 3 to 5 days of preparation.
When sample numbers are allowed, all crystallization conditions are performed in duplicate in a glass 96-well plate format; one half of each well plate is used to replicate the conditions in the other half of the well plate. Cross-contamination between wells is minimized by design. All conditions of the assay were reproducibly run in at least duplicate, most yielding solid material suitable for further analysis.
In all cases, the equipment in contact with the sample and the crystallization medium was carefully cleaned with various solvents and reagents, then soaked in ethanol and blown dry using a large amount of evaporated nitrogen.
High quality solvents from commercial suppliers were used as described in table 12.
TABLE 12
| Solvent(s) | Suppliers of goods | Product number | Batch number | Grade | Purity of |
| 1, 2-dichlorobenzene | Romil | H177 | E558470 | SpS | ＞99.8％ |
| 1, 4-xylene | Fluka | 95682 | 429739/1 | purissp.a. | ＞99％ |
| 1, 4-dioxane | Romil | H297 | H540480 | SpS | ＞99.9％ |
| 2, 2, 2-trifluoroethanol | Romil | H860 | M538412 | SpS | ＞99.9％ |
| Acetonitrile | Romil | H049 | D531490 | SpS | ＞99.9％ |
| Dimethylacetamide | Romil | H249 | B540480 | SpS | ＞99.9％ |
| Dimethyl sulfoxide | Romil | H280 | W530480 | SpS | ＞99.9％ |
| Ethanol | Romil | H314 | O533480 | SpS | ＞99.8％ |
| Ethyl acetate | Romil | H346 | T533480 | SpS | ＞99.9％ |
| Methyl isobutyl ketone | Romil | H446 | M539430 | SpS | ＞99.9％ |
| N-nonane | Romil | H568 | O558450 | SpS | ＞99.9％ |
| Acetic acid pentyl ester | Fluka | 46022 | 13248/1 | purissp.a. | ＞98.5％ |
| Propan-1-ol | Romil | H624 | G531460 | SpS | ＞99.9％ |
| Propan-2-ol | Romil | H625 | O530480 | SpS | ＞99.9％ |
| Tetrachloroethylene | Romil | H702 | W536450 | SpS | ＞99.9％ |
| Tetrahydrofuran (THF) | Romil | H718 | B532470 | SpS | ＞99.9％ |
| Acetone (II) | Romil | H031 | E559470 | SpS | ＞99.9％ |
| Chloroform | Romil | H135 | B554470 | SpS | ＞99.9％ |
| Methylene dichloride | Romil | H202 | O554460 | SpS | ＞99.9％ |
| Dimethyl formamide | Romil | H253 | T546460 | SpS | ＞99.9％ |
| Carboxamides | Romil | H351 | Q537480 | BioPure | ＞99.9％ |
| Hexafluoropropan-2-ol | Romil | H359 | H559470 | SpS | ＞99.9％ |
| Benzoic acid methyl ester | Fluka | 12460 | 417868/1 | purum | ＞98％ |
| Water (W) | Romil | H950 | D537480 | SpS | ＞99.9％ |
The resulting crystalline morphology was visually analyzed using a binocular microscope (approximately 10x-40x magnification) with a digital camera, using transmitted and reflected light as appropriate.
The visual characterization of the solid material is summarized in table 14 below. Advantageous blade or table/plate morphology is observed, either as distinct crystals or as pellets. Overall, there was little morphological difference between the crystallization carried out at ambient temperature and those carried out at 4 ℃, except for those with ethanol as solvent, where the tendency for spherulite and interfacial type growth decreased with decreasing temperature. Notably, the use of an anti-solvent can significantly improve the quality of the crystalline material.
An example image of the crystalline material observed is given in fig. 17. As shown in the figure, acetonitrile has a tendency to produce spherulite growth, which is generally seen as a result of poor nucleation and thus growth from poor quality crystalline surfaces. In contrast, 2-methoxyethanol has a tendency to produce unique crystals with a leaf/needle morphology.
Crystallization of form 1 from a number of conditions appears to be generally preferred. It is noteworthy, however, that form 2 was also observed from some crystallization conditions, including obtaining scaled-down analogs of forms 3 and 4 (described in example 6). Form 2 is observed under extreme conditions where polar (e.g. acetonitrile: water) or lipophilic (n-nonane) or both (dimethylsulfoxide: 1, 2-dichlorobenzene) are present. In general, crystals of type 2 are notable for their superior quality and specific well-formed plate/table format crystal forms.
Single crystal X-ray diffraction cell determination
To provide corroborative evidence of the resulting crystalline morphology, single crystal X-ray diffraction was used to determine the unit cell parameters for a number of crystals of suitable quality. Parameters of a single crystal of the crystal mounted on a glass fiber containing oil and held at 260k were measured with Mo radiation using a Kappa CCD diffractometer. The parameters for form 1 and form 2 have been determined as summarized in Table 13.
TABLE 13 unit cell parameters determined for crystals of benzenesulfonate salt of the compound of the formula (I)
The crystallization results of the benzenesulfonate salt of the compound of the general formula (I) from solvent/cosolvent and solvent/antisolvent conditions are tabulated in table 14 along with single crystal X-ray diffraction single crystal results.
Table 14 experimental crystallization results of benzenesulfonate salts of compounds of general formula (I) from solvent/cosolvent and solvent/antisolvent conditions, and single crystal X-ray diffraction single crystal results (X-ray results of ambient crystallization, unless otherwise specified).
For all single crystal X-ray diffraction crystal structure measurements, various crystals of suitable quality were obtained, and for types 1 and 2, all structures were obtained. These crystal structures are reported in examples 9 and 10.
Example 9
Crystal structure of type 1
Crystals of the benzenesulfonate salt of the compound of the formula (I), which have a needle-like crystal form, grown from a 2-methoxyethanol amyl acetate solution are imaged in fig. 17.
A single needle crystal form (approximately 0.8X 0.04X 0.02mm in size) was selected and its unit cell parameters were measured at 260K, then 190K. No transition was observed when the temperature was decreased between 260 ℃ and 190 ℃. The structure analyzed here was for data at 190K; the parameters of the crystals and the X-ray diffraction refinements are given in table 15.
TABLE 15 data for crystals grown from 2-methoxyethanol amyl acetate of the benzenesulfonate form 1 of the compound of the general formula (I).
The content of asymmetric units is shown in fig. 18. It consists of two separate molecules of the compound and two separate benzenesulfonate counter ions. The imidazole nitrogen of each compound is protonated.
The Flack "enertiopole" parameter was determined to be 0.03(1) and thus the stereochemistry of the structures depicted here was well established and consistent with the claimed stereochemistry of this compound:
crystallographic co-ordinates and other relevant data are tabulated in table 17 in the form of a SHELX file.
Conformational disorder can be represented (roughly) by the "thermal ellipsoid" of atomic positions, as given on fig. 19. It can be seen that the major regions of disorder are located in the methyl and benzene sulfonate.
The difference between the two independent molecules is mainly from the ester chain, as shown in figure 20. One molecule has ester chains that are coplanar with the imidazole rings, while the other molecule has ester chains that are orthogonal.
The conformation of the ester chain differs from the conformation adopted in type 2 (fig. 21). The orthogonal conformation observed in form 1 is most similar to that found in form 2.
Two independent benzenesulfonates had staggered conformations (fig. 22). It is clear that there is no considerable difference in bond length.
One benzenesulfonate adopted the conformation observed for benzenesulfonate in form 2 (fig. 23).
The resolved crystal structures observed along the crystallographic a, b and c axes are shown in fig. 24a, b and c, respectively. Fig. 25 summarizes the shortest contacts observed in crystal fill.
Each compound interacts with two independent benzenesulfonate salts. Specifically, a short distance (hydrogen bond type) is established between an oxygen atom of a benzenesulfonate and the protonated nitrogen of the imidazole ring of the compound. The second independent compound interacts similarly, but with the second independent benzenesulfonate salt.
Other intimate contacts (C-O, H-O) were observed between the compound and the benzenesulfonate salt, primarily near the imidazole and pyridyl rings. Some intimate contact is also observed between the two compounds themselves (Br-N, C-C, O-H) and the two benzenesulfonates themselves (O-H contact), but to a lesser extent.
Using experimentally determined crystal structures, have been used(CrystalDiffract is a registered trademark of CrystalMaker Ltd.) A powder diffraction pattern of type 1 was calculated and plotted in FIG. 26. This powder pattern matches the experimental powder pattern reported for type 1.
Example 10
Crystal structure of type 2
Crystals of the compound of formula (I) besylate form 2, which has a plate crystal form, are imaged in figure 27.
Single plate crystal form crystals (approximately 0.7 x 0.30 x 0.25mm in size) were selected and their unit cell parameters were determined at 260K, then 190K. No transition was observed when the temperature was decreased between 260 ℃ and 190 ℃. The structure analyzed here was for data at 190K; the parameters of the crystals and the X-ray diffraction refinements are given in table 16.
TABLE 16 data for crystals grown from EtOH/Ethyl acetate of the benzenesulfonate salt of the compound of the general formula (I) (form 2).
The content of asymmetric units is shown in fig. 28. It consists of one independent molecule of the compound and one independent benzenesulfonate salt. The imidazole nitrogen of the compound is protonated.
The Flack "enertiopole" parameter was determined to be 0.011(9) and thus the stereochemistry of the structures depicted herein is well established and consistent with the claimed stereochemistry of this compound. Crystallographic co-ordinates and other relevant data are tabulated in table 18 in the form of a SHELX file.
Conformational disorder can be represented (roughly) by the "thermal ellipsoid" of atomic positions, as given on fig. 29. It can be seen that the main region of disorder is located in the benzenesulfonate salt.
As discussed above, the conformation of the ester chains in form 2 (plotted in figure 30) differs from the conformation adopted in form 1.
However, the conformation of the benzenesulfonate was similar to that observed for one of the benzenesulfonates in form 1 (fig. 31).
The resolved crystal structures observed along the crystallographic a, b and c axes are shown in fig. 32a, b and c, respectively, where fig. 33 summarizes the shortest contacts observed in the crystal fill. The compound is in short contact (hydrogen bond type) with one oxygen atom of the benzenesulfonate via the protonated nitrogen of the imidazole ring. Other short contacts via the imidazole ring were observed between the compound and the benzenesulfonate (C-C, C-O, H-O).
Some intimate contact is also observed between the two compounds themselves (Br-C, C-C, O-C, O-H), most of them via an ester chain. There is no intimate contact between the benzenesulfonate salts themselves.
Using experimentally determined crystal structures, have been usedThe powder diffraction pattern of type 2 was calculated (fig. 34). This powder pattern matches the experimental powder pattern reported for type 2.
TABLE 17 crystallographic co-ordinates tabulated in SHELX file for compound besylate dosage form 1 of formula (I) and other pertinent data.
TITL 12161316 compound CNS7056Model (III)
CELL 0.71073 7.687 29.261 12.376 90.000 97.788 90.000
ZERR 2 0.0001 0.0005 0.0003 0.0000 0.0008 0.0000
LATT -1
SYMM -X，Y+0.500，-Z
SFAC C 2.3100 20.8439 1.0200 10.2075 1.5886
0.5687 0.8650＝
51.6512 0.2156 0.0033 0.0016 1.15
0.7700 12.0110
SFAC H 0.4930 10.5109 0.3229 26.1257 0.1402
3.1424 0.0408＝
57.7998 0.0030 0.0000 0.0000 0.06
0.3200 1.0079
SFAC O 3.0485 13.2771 2.2868 5.7011 1.5463
0.3239 0.8670＝
32.9089 0.2508 0.0106 0.0060 3.25
0.7700 15.9994
SFAC BR 17.1789 2.1723 5.2358 16.5796 5.6377
0.2609 3.9851＝
41.4328 2.9557 -0.2901 2.4595 1000.00
1.1000 79.9040
SFAC N 12.2126 0.0057 3.1322 9.8933 2.0125
28.9975 1.1663＝
0.5826 -11.5290 0.0061 0.0033 1.96
0.7700 14.0067
SFAC S 6.9053 1.4679 5.2034 22.2151 1.4379
0.2536 1.5863＝
56.1720 0.8669 0.1246 0.1234 53.20
1.1100 32.0660
UNIT 108.100.20.4.16.4.
S80 6 0.23964 0.43139 0.09908 11.00000
0.04634 0.03299＝
0.04052 0.00002 0.01880 -0.00340
O81 3 0.16028 0.39374 0.15143 11.00000
0.06864 0.04111＝
0.05255 -0.00210 0.02801 0.00002
O82 3 0.14598 0.47435 0.11207 11.00000
0.08099 0.03603＝
0.04614 0.00545 0.03373 -0.00236
O83 3 0.42589 0.43401 0.12925 11.00000
0.05754 0.08564＝
0.05198 -0.01536 0.01792 -0.00644
C84 1 0.20581 0.41866 -0.04324 11.00000
0.05949 0.04444＝
0.02903 0.00359 0.01728 0.00704
C85 1 0.03624 0.41100 -0.09142 11.00000
0.06649 0.10092＝
0.05586 0.01088 0.01751 0.00507
C86 1 0.00323 0.39810 -0.20187 11.00000
0.08670 0.14765＝
0.05902 -0.02096 -0.03160 -0.00004
C87 1 0.14311 0.39209 -0.25693 11.00000
0.07916 0.11651＝
0.06238 -0.01696 0.00195 0.02481
C88 1 0.30473 0.39806 -0.20987 11.00000
0.09246 0.09710＝
0.04155 0.00157 0.01795 0.02685
C89 1 0.33456 0.41126 -0.10133 11.00000
0.05999 0.09817＝
0.07178 -0.01451 0.00886 0.02173
S90 6 0.68868 0.81145 0.51625 11.00000
0.04072 0.02869＝
0.05437 0.00158 0.00214 0.00223
O91 3 0.79129 0.77464 0.57315 11.00000
0.08025 0.03751＝
0.04867 -0.00213 -0.00954 0.01626
O92 3 0.52601 0.81933 0.56122 11.00000
0.04778 0.05360＝
0.06934 -0.00642 0.01702 0.00039
O93 3 0.78935 0.85213 0.50763 11.00000
0.07515 0.04369＝
0.05025 -0.01354 0.01764 -0.01547
C94 1 0.62446 0.78970 0.38130 11.00000
0.04232 0.04028＝
0.05049 0.00898 0.00929 0.00525
C95 1 0.74659 0.76959 0.32396 11.00000
0.06194 0.06998＝
0.03238 0.00341 -0.00103 0.00990
C96 1 0.69911 0.75023 0.22476 11.00000
0.12417 0.10337＝
0.03441 0.01537 0.02421 0.03314
C97 1 0.51941 0.75295 0.17732 11.00000
0.11897 0.11939＝
0.02308 -0.01324 -0.00963 -0.00586
C98 1 0.40301 0.77268 0.23169 11.00000
0.06106 0.10242＝
0.05463 0.00570 -0.01263 -0.00283
C99 1 0.45446 0.79193 0.33547 11.00000
0.05307 0.07089＝
0.04982 0.00728 -0.00426 -0.01944
BR1 4 0.06011 0.52462 0.55140 11.00000
0.04153 0.05204＝
0.07369 -0.00524 0.02434 0.00670
C2 1 0.25757 0.50395 0.49005 11.00000
0.02832 0.04536＝
0.03350 -0.00752 0.01511 0.00763
C3 1 0.28921 0.45781 0.47911 11.00000
0.03135 0.03107＝
0.04579 0.00145 0.00221 -0.00479
C4 1 0.42954 0.44393 0.43174 11.00000
0.03767 0.03461＝
0.02980 -0.00320 -0.00151 -0.00125
C5 1 0.54674 0.47556 0.39943 11.00000
0.03535 0.02939＝
0.03479 -0.00390 0.00647 0.00183
C6 1 0.51907 0.52242 0.41134 11.00000
0.04226 0.03479＝
0.04333 -0.00172 0.00236 0.00188
C7 1 0.37213 0.53602 0.45794 11.00000
0.03598 0.02793＝
0.04586 -0.00044 0.01652 0.00336
C8 1 0.64321 0.55824 0.38118 11.00000
0.03964 0.02453＝
0.02719 0.00516 0.00457 0.00373
C9 1 0.68998 0.59645 0.46059 11.00000
0.03743 0.03694＝
0.04454 -0.00375 0.01588 0.00649
N10 5 0.69097 0.58514 0.56581 11.00000
0.06070 0.03116＝
0.04918 -0.00640 0.02020 -0.00054
C11 1 0.74090 0.61847 0.63822 11.00000
0.06804 0.05787＝
0.04752 -0.00600 0.01695 -0.00669
C12 1 0.78515 0.66221 0.61053 11.00000
0.05480 0.04458＝
0.05526 -0.02125 0.01554 -0.00787
C13 1 0.77550 0.67229 0.50132 11.00000
0.04463 0.03102＝
0.05452 0.00407 0.01432 -0.00038
C14 1 0.73186 0.63955 0.42553 11.00000
0.04272 0.03021＝
0.04282 -0.00243 0.01499 0.00270
N15 5 0.71451 0.55972 0.29408 11.00000
0.04979 0.02502＝
0.03692 0.00975 0.01748 0.00775
C16 1 0.67500 0.52204 0.21324 11.00000
0.04463 0.02346＝
0.04948 -0.00464 0.01738 0.00561
C17 1 0.75857 0.47996 0.26673 11.00000
0.04549 0.02673＝
0.01954 -0.00693 0.00506 -0.00121
N18 5 0.70009 0.45973 0.35317 11.00000
0.03293 0.02806＝
0.02597 -0.00088 0.00321 0.00207
C19 1 0.81334 0.42409 0.39181 11.00000
0.03678 0.02848＝
0.03351 -0.00426 0.00585 0.00488
C20 1 0.93968 0.42402 0.32661 11.00000
0.03371 0.02802＝
0.03711 0.00202 0.00106 0.00680
N21 5 0.90585 0.45925 0.25315 11.00000
0.04775 0.03416＝
0.02231 -0.01051 0.01052 -0.00308
C22 1 0.79597 0.39511 0.48941 11.00000
0.03997 0.03711＝
0.04548 0.01039 0.00508 0.00197
C23 1 0.74788 0.53407 0.10940 11.00000
0.05650 0.04712＝
0.03514 0.00836 0.00449 0.00605
C24 1 0.68780 0.50047 0.01647 11.00000
0.08242 0.04077＝
0.03001 -0.00046 0.01385 0.00523
C25 1 0.71419 0.51690 -0.09234 11.00000
0.06429 0.06543＝
0.03392 0.00018 0.00559 -0.00499
O26 3 0.76261 0.55440 -0.11450 11.00000
0.12347 0.08282＝
0.04188 0.01501 0.01658 -0.04001
O27 3 0.65910 0.48459 -0.16756 11.00000
0.10340 0.06919＝
0.03191 0.00253 0.01824 -0.00449
C28 1 0.66642 0.49760 -0.27953 11.00000
0.19131 0.12699＝
0.01390 -0.01417 0.02134 -0.05279
BR51 4 1.06737 0.71057 0.98743 11.00000
0.03812 0.08781＝
0.06774 0.00566 -0.00531 0.00447
C52 1 0.84276 0.73306 0.93243 11.00000
0.03132 0.05952＝
0.03819 0.00358 0.00226 -0.00263
C53 1 0.81293 0.77906 0.93249 11.00000
0.04627 0.06820＝
0.03723 -0.00581 0.00481 -0.00474
C54 1 0.65043 0.79579 0.88269 11.00000
0.04551 0.03939＝
0.04858 -0.00084 0.00376 -0.01071
C55 1 0.51946 0.76552 0.84226 11.00000
0.04294 0.03573＝
0.03413 0.00062 0.00952 -0.00208
C56 1 0.54512 0.71765 0.84581 11.00000
0.02688 0.03659＝
0.04586 -0.00025 0.00561 0.00047
C57 1 0.71139 0.70186 0.88914 11.00000
0.03105 0.04840＝
0.04447 -0.00668 -0.00429 0.00504
C58 1 0.40956 0.68443 0.79765 11.00000
0.03348 0.02893＝
0.04334 0.00070 0.00351 0.00421
C59 1 0.38048 0.64253 0.86694 11.00000
0.03165 0.03488＝
0.04951 0.00002 0.00425 0.00528
N60 5 0.42879 0.64650 0.97247 11.00000
0.03542 0.05694＝
0.03178 0.00872 0.00154 0.00467
C61 1 0.38962 0.61026 1.03529 11.00000
0.04457 0.06338＝
0.05765 0.01416 0.00707 0.00171
C62 1 0.30187 0.57202 0.98967 11.00000
0.06548 0.04957＝
0.11303 0.03456 0.03582 0.00696
C63 1 0.25733 0.56863 0.88018 11.00000
0.07395 0.04664＝
0.09803 0.00115 0.01240 -0.01007
C64 1 0.29561 0.60475 0.81590 11.00000
0.08355 0.04152＝
0.05459 -0.00010 0.00128 -0.02308
N65 5 0.31344 0.68797 0.70771 11.00000
0.03846 0.03072＝
0.04952 -0.00160 0.00032 0.00597
C66 1 0.33129 0.72953 0.64125 11.00000
0.03574 0.02676＝
0.05519 0.00406 0.00580 0.00330
C67 1 0.26347 0.76733 0.70231 11.00000
0.03803 0.03316＝
0.04166 0.01528 0.00868 0.00029
N68 5 0.35122 0.78274 0.79764 11.00000
0.03387 0.03259＝
0.05055 0.00549 0.00427 0.00218
C69 1 0.24763 0.81583 0.84108 11.00000
0.05345 0.03305＝
0.04570 0.00005 0.02067 -0.00546
C70 1 0.09873 0.81841 0.77077 11.00000
0.04465 0.03799＝
0.06107 0.00794 0.01464 0.00936
N71 5 0.10819 0.78841 0.68720 11.00000
0.03892 0.03266＝
0.05306 0.00974 0.01063 0.00803
C72 1 0.30218 0.84064 0.94469 11.00000
0.08091 0.04934＝
0.08052 -0.01505 0.02392 -0.00661
C73 1 0.22541 0.72388 0.52948 11.00000
0.04039 0.05583＝
0.03295 0.00047 0.00724 -0.00165
C74 1 0.30154 0.68566 0.46508 11.00000
0.05896 0.05343＝
0.05504 -0.00576 0.00667 0.02016
C75 1 0.18003 0.67204 0.36587 11.00000
0.05296 0.05447＝
0.04241 0.00546 0.01355 0.00171
O76 3 0.06782 0.69497 0.31818 11.00000
0.05552 0.07543＝
0.05719 -0.00702 -0.00194 0.02108
O77 3 0.22119 0.62976 0.33149 11.00000
0.08466 0.04267＝
0.04376 -0.00714 0.00726 0.00488
C78 1 0.10717 0.61220 0.23887 11.00000
0.06302 0.09312＝
0.07465 -0.02449 0.02418 -0.00980
H611 2 10.42342 10.61111 11.10933 11.00000
0.06582
H621 2 10.27371 10.54835 11.03412 11.00000
0.09086
H631 2 10.20282 10.54235 10.84949 11.00000
0.08585
H641 2 10.26600 10.60396 10.74163 11.00000
0.07058
H661 2 10.45616 10.73494 10.63683 11.00000
0.04658
H701 2 10.00528 10.83765 10.77749 11.00000
0.05724
H721 2 10.20390 10.85662 10.96784 11.00000
0.10482
H722 2 10.39143 10.86250 10.93477 11.00000
0.10500
H723 2 10.34863 10.81975 11.00178 11.00000
0.10479
H731 2 10.22647 10.75279 10.49048 11.00000
0.05050
H732 2 10.10462 10.71635 10.53573 11.00000
0.05107
H741 2 10.41143 10.69632 10.44327 11.00000
0.06599
H742 2 10.32279 10.65905 10.51273 11.00000
0.06616
H571 2 10.73613 10.67093 10.88928 11.00000
0.04893
H531 2 10.89874 10.79871 10.96543 11.00000
0.05990
H541 2 10.63029 10.82681 10.87790 11.00000
0.05285
H161 2 10.54702 10.51731 10.19609 11.00000
0.04687
H201 2 11.03302 10.40374 10.33036 11.00000
0.03977
H221 2 10.90306 10.37871 10.51025 11.00000
0.06107
H222 2 10.77354 10.41394 10.54853 11.00000
0.06102
H223 2 10.70245 10.37370 10.47387 11.00000
0.06087
H231 2 10.71028 10.56434 10.08666 11.00000
0.05487
H232 2 10.87494 10.53365 10.12431 11.00000
0.05471
H241 2 10.56546 10.49241 10.01723 11.00000
0.06095
H242 2 10.75795 10.47323 10.02815 11.00000
0.06099
H111 2 10.74728 10.61186 10.71244 11.00000
0.06882
H121 2 10.81997 10.68398 10.66349 11.00000
0.06182
H131 2 10.79812 10.70154 10.48020 11.00000
0.05215
H141 2 10.72939 10.64544 10.35226 11.00000
0.04595
H71 2 10.35042 10.56684 10.46668 11.00000
0.04408
H31 2 10.21444 10.43638 10.50355 11.00000
0.04223
H41 2 10.44931 10.41280 10.42055 11.00000
0.04056
H891 2 10.44977 10.41481 9.93226 11.00000
0.09285
H881 2 10.39917 10.39332 9.75106 11.00000
0.09266
H871 2 10.12372 10.38356 9.66972 11.00000
0.10194
H861 2 9.88808 10.39388 9.76390 11.00000
0.11607
H851 2 9.94416 10.41466 9.94909 11.00000
0.08904
H951 2 10.86472 10.76918 10.35546 11.00000
0.06580
H961 2 10.78321 10.73544 10.18942 11.00000
0.10497
H971 2 10.48493 10.74055 10.10914 11.00000
0.10604
H981 2 10.28646 10.77378 10.20054 11.00000
0.08719
H991 2 10.37377 10.80653 10.37249 11.00000
0.07037
H781 2 10.14480 10.58182 10.22240 11.00000
0.11588
H782 2 10.11102 10.63197 10.17669 11.00000
0.11581
H783 2 9.98883 10.61082 10.25546 11.00000
0.11600
H711 2 10.01359 10.78308 10.62464 11.00000
0.05205
H211 2 10.98261 10.46785 10.19729 11.00000
0.04161
H281 2 10.62358 10.47180 9.67092 11.00000
0.11566
H282 2 10.59036 10.52501 9.70225 11.00000
0.11566
H283 2 10.79029 10.50514 9.71088 11.00000
0.11566
TABLE 18 Benzenesulfonate salt of the compound of formula (I) in SHELX file formCrystallographic co-ordinates of the formulary and other relevant data.
TITL 1142055 compound CNS7056 dosage form 1
CELL 0.71073 8.921 11.154 25.834 90.000 90.000 90.000
ZERR 4 0.0001 0.0002 0.0004 0.0000 0.0000 0.0000
LATT -1
SYMM X+0.500，-Y+0.500，-Z
SYMM -X，Y+0.500，-Z+0.500
SYMM -X+0.500，-Y，Z+0.500
SFAC C 2.3100 20.8439 1.0200 10.2075 1.5886
0.5687 0.8650＝
51.6512 0.2156 0.0033 0.0016 1.15
0.7700 12.0110
SFAC H 0.4930 10.5109 0.3229 26.1257 0.1402
3.1424 0.0408＝
57.7998 0.0030 0.0000 0.0000 0.06
0.3200 1.0079
SFAC BR 17.1789 2.1723 5.2358 16.5796 5.6377
0.2609 3.9851＝
41.4328 2.9557 -0.2901 2.4595 1000.00
1.1000 79.9040
SFAC N 12.2126 0.0057 3.1322 9.8933 2.0125
28.9975 1.1663＝
0.5826 -11.5290 0.0061 0.0033 1.96
0.7700 14.0067
SFAC O 3.0485 13.277 12.2868 5.7011 1.5463
0.3239 0.8670＝
32.9089 0.2508 0.0106 0.0060 3.25
0.7700 15.9994
SFAC S 6.9053 1.4679 5.2034 22.2151 1.4379
0.2536 1.5863＝
56.1720 0.8669 0.1246 0.1234 53.20
1.1100 32.0660
UNIT 108.100.4.16.20.4.
BR1 3 -0.04819 -0.10880 -0.27710 11.00000
0.07032 0.03277＝
0.03090 0.00144 -0.01238 -0.02224
C2 1 -0.15018 -0.21830 -0.32054 11.00000
0.02777 0.02177＝
0.02345 -0.00009 -0.00209 -0.00471
C3 1 -0.17401 -0.18875 -0.37205 11.00000
0.02963 0.01861＝
0.02702 0.00623 0.00188 -0.00107
C4 1 -0.24491 -0.26965 -0.40362 11.00000
0.02825 0.02442＝
0.01718 0.00327 0.00106 -0.00145
C5 1 -0.29275 -0.37943 -0.38401 11.00000
0.02223 0.01822＝
0.01875 -0.00067 0.00141 0.00066
C6 1 -0.27139 -0.40894 -0.33163 11.00000
0.02028 0.01967＝
0.01926 0.00182 0.00105 -0.00153
C7 1 -0.20042 -0.32532 -0.29979 11.00000
0.02809 0.02763＝
0.01685 0.00206 0.00190 -0.00055
C8 1 -0.32197 -0.52600 -0.30927 11.00000
0.01670 0.02233＝
0.01945 0.00135 -0.00476 -0.00144
C9 1 -0.39853 -0.52353 -0.25770 11.00000
0.01623 0.02317＝
0.01584 0.00259 -0.00384 -0.00281
N10 4 -0.46099 -0.41943 -0.24363 11.00000
0.02251 0.02613＝
0.02353 -0.00189 0.00408 0.00155
C11 1 -0.52777 -0.41652 -0.19697 11.00000
0.02617 0.03441＝
0.02357 -0.00451 0.00365 0.00346
C12 1 -0.53610 -0.51390 -0.16425 11.00000
0.02740 0.04329＝
0.02040 -0.00335 0.00652 -0.00779
C13 1 -0.47518 -0.62062 -0.17997 11.00000
0.03584 0.03200＝
0.02405 0.00767 0.00645 -0.00687
C14 1 -0.40334 -0.62685 -0.22730 11.00000
0.02879 0.02223＝
0.02565 0.00090 0.00272 -0.00057
N15 4 -0.30040 -0.62781 -0.33049 11.00000
0.02151 0.02416＝
0.01713 0.00287 -0.00002 0.00182
C16 1 -0.21928 -0.62991 -0.38036 11.00000
0.02330 0.02286＝
0.01602 0.00057 0.00417 0.00450
C17 1 -0.32510 -0.57975 -0.41920 11.00000
0.02824 0.02308＝
0.01704 -0.00121 0.00336 -0.00285
N18 4 -0.36294 -0.46298 -0.41818 11.00000
0.02482 0.02037＝
0.01483 0.00150 -0.00070 0.00079
C19 1 -0.46920 -0.44117 -0.45641 11.00000
0.03022 0.02725＝
0.01634 0.00325 0.00039 -0.00224
C20 1 -0.49445 -0.54753 -0.47911 11.00000
0.03071 0.03401＝
0.01669 0.00110 -0.00174 -0.00215
N21 4 -0.40440 -0.63226 -0.45591 11.00000
0.03619 0.02354＝
0.02146 -0.00463 0.00147 -0.00154
C22 1 -0.5431 0-0.32298 -0.46595 11.00000
0.03636 0.03429＝
0.03074 0.00778 -0.00982 -0.00011
C23 1 -0.15995 -0.75547 -0.39193 11.00000
0.03430 0.02640＝
0.01793 -0.00359 0.00177 0.00554
C24 1 -0.06166 -0.79435 -0.34621 11.00000
0.04707 0.03881＝
0.02350 0.00041 0.00034 0.01530
C25 1 0.06625 -0.87542 -0.35603 11.00000
0.03182 0.02650＝
0.01948 0.00340 -0.00125 -0.00016
O26 5 0.17233 -0.88334 -0.32760 11.00000
0.03778 0.06570＝
0.03313 -0.01160 -0.01173 0.00417
O27 5 0.05245 -0.94265 -0.39885 11.00000
0.03130 0.03874＝
0.02467 -0.00799 -0.00330 0.01418
C28 1 0.17574 -1.02443 -0.40865 11.00000
0.05622 0.08123＝
0.03697 -0.01153 -0.00496 0.04396
S80 6 -0.94275 -0.52899 -0.49624 11.00000
0.03340 0.02679＝
0.02442 0.00000 0.00210 -0.00075
O81 5 -0.83867 -0.47114 -0.53020 11.00000
0.05118 0.08336＝
0.03575 0.02297 -0.00622 -0.02476
O82 5 -1.08156 -0.46260 -0.49186 11.00000
0.04015 0.07788＝
0.05503 -0.01022 -0.00539 0.01721
O83 5 -0.97025 -0.65272 -0.50726 11.00000
0.13945 0.03230＝
0.06071 -0.01467 0.01447 -0.00725
C84 1 -0.86288 -0.52210 -0.43343 11.00000
0.02735 0.05893＝
0.02832 0.01509 0.00686 -0.00534
C85 1 -0.87781 -0.41462 -0.40588 11.00000
0.03763 0.08695＝
0.03855 -0.01799 0.00427 -0.00754
C86 1 -0.81420 -0.39965 -0.35764 11.00000
0.05438 0.16315＝
0.04455 -0.02905 0.00147 -0.02905
C87 1 -0.73766 -0.49241 -0.33773 11.00000
0.06202 0.20226＝
0.06481 0.03510 -0.02105 -0.05062
C88 1 -0.71885 -0.60444 -0.36221 11.00000
0.04217 0.17120＝
0.11388 0.10762 -0.01320 -0.03729
C89 1 -0.78500 -0.61610 -0.41251 11.00000
0.03725 0.08786＝
0.07642 0.05538 -0.00772 -0.01074
H891 2 9.22557 9.31210 9.56883 11.00000
0.08027
H881 2 9.33331 9.33306 9.65289 11.00000
0.13097
H851 2 9.06867 9.64846 9.57936 11.00000
0.06577
H861 2 9.17563 9.67239 9.66111 11.00000
0.10509
H161 2 9.86530 9.42517 9.62245 11.00000
0.02469
H111 2 9.42959 9.65626 9.81326 11.00000
0.03383
H121 2 9.41618 9.49292 9.86839 11.00000
0.03606
H131 2 9.51614 9.31066 9.84059 11.00000
0.03697
H141 2 9.64103 9.30191 9.76144 11.00000
0.03108
H231 2 9.89972 9.24922 9.57680 11.00000
0.03066
H232 2 9.75764 9.18723 9.60372 11.00000
0.03099
H241 2 9.87585 9.16237 9.67759 11.00000
0.04434
H242 2 9.97980 9.27746 9.67100 11.00000
0.04489
H281 2 10.15353 8.92912 9.56085 11.00000
0.08666
H282 2 10.18989 8.92278 9.62053 11.00000
0.08723
H283 2 10.26566 9.02166 9.58620 11.00000
0.08710
H201 2 9.44027 9.43682 9.49457 11.00000
0.03327
H221 2 9.36727 9.66624 9.51370 11.00000
0.05146
H222 2 9.52479 9.72860 9.51527 11.00000
0.05104
H223 2 9.43193 9.71611 9.56601 11.00000
0.05131
H41 2 9.73983 9.74902 9.56204 11.00000
0.02807
H31 2 9.85823 9.88568 9.61518 11.00000
0.03001
H71 2 9.81367 9.65791 9.73490 11.00000
0.02870
H871 2 9.30621 9.51762 9.69480 11.00000
0.13226
H211 2 9.59801 9.29339 9.53630 11.00000
0.03270
TABLE 19 benzenesulfonate salts of compounds of the general formula (I)Type bond length.
TABLE 20 benzenesulfonate salts of compounds of the general formula (I)Angle of the model
TABLE 21 benzenesulfonate salts of compounds of the general formula (I)Type bond length.
TABLE 22 benzenesulfonate salts of compounds of the general formula (I)Angle of the model
Claims (10)
1. A crystalline benzenesulfonate salt of a compound of the following formula (I):
it is a crystalline form having an X-ray powder diffraction pattern obtained using Cu ka radiation substantially as shown in figure 11.
2. The crystalline benzenesulfonate salt according to claim 1, which exhibits an X-ray powder diffraction pattern obtained using Cu ka radiation, including characteristic peaks located at 7.3, 7.8, 9.4, 12.1, 14.1, 14.4, 14.7 and 15.6 degrees 2 Θ.
3. The crystalline benzenesulfonate salt according to claim 1 or 2, which exhibits an X-ray powder diffraction pattern obtained using Cu ka radiation, comprising characteristic peaks at 7.25, 7.84, 9.36, 12.13, 14.06, 14.41, 14.70 and 15.60 degrees 2 Θ, the relative intensities of these characteristic peaks being 10.60, 72.60, 12.10, 32.50, 48.50, 74.30, 50.70 and 26.90, respectively.
4. The crystalline benzenesulfonate salt according to claim 1, which comprises crystals having the following unit cell sizes:
5. the crystalline benzenesulfonate salt according to claim 1, comprising crystals in the form according to P21A monoclinic crystal system of space group.
6. The crystalline benzenesulfonate salt according to claim 1, which comprises 2757.86(9) in volumeThe crystal of (4).
7. The crystalline benzenesulfonate salt according to claim 1, which contains a calculated density of 1.439 g/cm3The crystal of (4).
8. The crystalline benzenesulfonate salt according to claim 1, comprising crystals each comprising two separate molecules of the compound and two molecules of the benzenesulfonate salt per asymmetric unit.
9. The crystalline benzenesulfonate salt according to claim 1, having a crystal structure defined by the structure coordinates set forth in the following table:
10. the crystalline benzenesulfonate salt according to claim 1, having a crystal structure with bond lengths and angles as shown in the following table:
bond length:
angle:
。
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB0613692.3 | 2006-07-10 | ||
| GB0613694A GB0613694D0 (en) | 2006-07-10 | 2006-07-10 | Benzodiazepine salts |
| GB0613694.9 | 2006-07-10 | ||
| GB0613692A GB0613692D0 (en) | 2006-07-10 | 2006-07-10 | Benzodiazepine salts |
| PCT/GB2007/002565 WO2008007071A1 (en) | 2006-07-10 | 2007-07-10 | Short-acting benzodiazepine salts and their polymorphic forms |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| HK1137739A1 HK1137739A1 (en) | 2010-08-06 |
| HK1137739B true HK1137739B (en) | 2015-02-06 |
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