Title of Invention

"CRYSTALLINE SOLID FORM OF [2S, 5Z]-2-AMINO-7-[ETHANIMIDOYLAMINO]-2-METHYLHEPT-5-ENOIC ACID AND ITS METHOD OF PREPARATION"

Abstract A crystal form of 2-amino-7-(ethanimidoylamino)-2-methythept-5-enoic acid.
Full Text The present invention relates to crystalline solid form of [2S,5Z]-2-amino-7-[ethanimidoylamino]-2-methylhept-5-enoic acid and its method of preparation.
Field of the Invention
The present invention comprises a novel compound useful in the treatment of disease, and more particularly a novel salt of (2S,5Z)-2-arnino-7-(ethanimidoylamino)-2-methylhept-5-enoic acid hydrochloride, and pharmaceutical compositions thereof, for the treatment of conditions involving an inappropriate expression of nitric oxide from the inducible isoform of nitric oxide synthase. (2S,5Z)-2-amino-7-(ethaiurnidoylarnino)-2-methyIhept-5-enoic acid is described and claimed in commonly assigned U.S. serial number 09/953,049, filed September 15, 2001, which claims priority to U.S. Provisional serial number 60/232,683, filed September 15, 2000, both herein incorporated by reference. (2S,5Z)-2-amino-7-(etharjirmdoylamino)-2-merhyIhept-5-enoic acid is also described in international publication number WO 02/22562, published March 21, 2002, which is a publication of commonly assigned international patent application PCT/US0128673, filed September 15,2001 and incorporated herein by reference.
Background of the Invention
Nitric oxide (NO) is a bioactive free radical gas produced by any one of several isoforms of the enzyme nitric oxide synthase (NOS). The physiological activity of what was later identified as NO was initially discovered in the early 1980's when it was found that vascular relaxation caused by acetylcholine is dependent on the presence of the vascular endothelium. The factor derived from the endothelium, then called endothelium-derived relaxing factor (EDRF), that mediates such vascular relaxation is now known to be NO that is generated in the vascular endothelium by one isoform of NOS. The activity of NO as a vasodilator has been known for well over 100 years. In addition, NO is the active species derived from known nitrovasodilators including amylnitrite, and glyceryltrinitrate. Nitric oxide is also an endogenous stimulator of soluble guanylate cyclase (cGMP), and thus stimulates cGMP production. When NOS is inhibited by N-monomethylarginine (L-NMMA), cGMP formation is completely prevented. In addition to endothelium-dependent relaxation, NO is known to be
involved in a number of biological actions including cytotoxicity of phagocyu'c cells and cell-to-cell communication in the central nervous system.
The identification of EDRF as NO coincided with the discovery of a biochemical pathway by which NO is synthesized from the amino acid L-arginine by the enzyme NO synthase. There are at least three types of NO synthase as follows:
(i) a constitutive, Ca++/calmodulin dependent enzyme, located in the brain, that releases NO in response to receptor or physical stimulation;
(ii) a Ca++ independent enzyme, a 130 kD protein, which is induced after activation of vascular smooth muscle, macrophages, endothelial cells, and a number of other cells by endotoxin and cytokines; and
(iii) a constitutive, Ca++/calmodulin dependent enzyme, located in the endothelium, that releases NO in response to receptor or physical stimulation.
Once expressed, inducible nitric oxide synthase (hereinafter "iNOS") generates NO continuously for long periods. Clinical studies have shown that NO production and iNOS expression are increased in a variety of chronic inflammatory diseases, such as rheumatoid and osteoarthritis (see, e.g, Mclnnes L B. et al, J. Exp. Med. 184:1519 (1996)), inflammatory bowel disease (see, e.g, Lundberg J. O. N. et al., Lancet 344:1673, (1994)), and asthma (see, e.g., Hamid, Q. et al., Lancet 342:1510 (1993)), and iNOS is implicated as a major pathological factor in these chronic inflammatory diseases.
Thus, inhibition of excessive NO production by iNOS is likely to be anti-inflammatory. However, since the production of NO from eNOS and nNOS is involved in normal physiology, it would be desirable for any NOS inhibitor that is used for treating inflammation be selective for iNOS, so that normal physiological modulation of blood pressure by eNOS-generated NO, and non-adrenergic, non-cholinergjc neuronal transmission by nNOS-generated NO would remain unaffected.
With all pharmaceutical compounds and compositions, the chemical and physical stability of a drug compound is important in the commercial development of that drug substance. Such stability includes the stability at ambient conditions, especially to moisture and under storage conditions. Elevated stability at different conditions of storage is needed to predict the different possible storage conditions during the lifetime of a commercial product. A stable drug avoids the use of special storage conditions as well as frequent inventory replacement. A drug compound must also be stable during the
manufacturing process which often requires milling of the drug to achieve drug material with uniform particle size and surface area. Unstable materials often undergo polymorphic changes. Therefore, any modification of a drug substance which enhances its stability profile provides a meaningful benefit over less stable substances.
Several inhibitors of iNOS have been described, such as, for example, 2S,5Z)-2-amino-7-(ethanimidoylamino)-2-methylhept-5-enoic acid, which is described in commonly assigned international publication number WO 02/22562, published March 21,2002, which is a publication of international patent application PCT/US0128673, filed September 15,2001. That compound, however, is an amorphous solid. It would be desirable, therefore, to provide a crystalline solid form of an iNOS inhibitor such as 2S,5Z)-2-animo-7-(ernanirmdoylamrno)-2-methylhept-5-enoic acid.
Summary of the Invention
The present invention is directed to a novel crystalline salt of (2S,5Z)-2-amino-7-(ethanimidoylamino)-2-methylhept-5-enoic acid hydrochloride, pharmaceutical
compositions, a process for preparing the novel salt compounds, a process for preparing
pharmaceutical compositions, and methods of using said novel salt compound and compositions for inhibiting or modulating nitric oxide synthesis in a subject in need of such inhibition or modulation by administering a salt of a compound which preferentially inhibits or modulates the inducible isoform of nitric oxide synthase over the constitutive isofonns of nitric oxide synthase. The present salt compound possesses useful nitric oxide synthase inhibiting activity, and is expected to be useful in the treatment or prophylaxis of a disease or condition in which the synthesis or oversynthesis of nitric oxide forms a contributory part.
Stoichiometrically, a unit cell of the novel salt is two molecules of (2S,5Z)-2-amino-7-(ethanimidoylamino)-2-methylhept-5-enoic acid and three molecules of hydrochloric acid.
The novel salt is characterized by some or all of the following physical measurements: elemental analysis (such as by combustion analysis), melting point and heat of fusion (differential scanning calorimetry and thermogravimetric analysis), refractive indices (polarized light microscopy), x-ray powder diffraction pattern, moisture sorption (for example, DVS moisture balance) and vibrational signature (Raman spectrum).
The present novel salt can be used to treat diseases involving cartilage degeneration, which takes place in certain conditions such as arthritis. Accordingly, conditions in which there is an advantage in inhibiting NO production from L-arginine include arthritic-conditions such as rheumatoid arthritis, osteoarthritis, gouty arthritis, juvenile arthritis, septic arthritis, spondyloarthritis, acute rheumatic arthritis, enteropathic arthritis, neuropathic arthritis, and pyogenic arthritis. In addition, NO-induced depression of chondrocyte respiration could modulate matrix loss and secondary cartilage mineralization in arthritis, in particular osteoarthritis.
Other conditions for which the present salt may be useful include chronic or inflammatory bowel disease, cardiovascular ischemia, diabetes, congestive heart failure, myocarditis, atherosclerosis, migraine, glaucoma, aortic aneurysm, reflux esophagitis, diarrhea, irritable bowel syndrome, cystic fibrosis, emphysema, asthma, bronchiectasis, hyperalgesia, cerebral ischemia, thrombotic stroke, global ischemia (secondary to cardiac arrest), multiple sclerosis and other central nervous system disorders mediated by NO, for example Parkinson's disease and Alzheimer's disease. Further neurodegenerative
disorders in which NO inhibition may be useful include nerve degeneration and/or nerve
necrosis in disorders such as hypoxia, hypoglycemia, epilepsy, and in external wounds
(such as spinal cord and head injury), hyperbaric oxygen convulsions and toxicity, dementia e.g. pre-senile dementia, and AIDS-related dementia, Sydenham's chorea, Huntington's disease, Amyotrophic Lateral Sclerosis, Korsakoff s disease, imbecility relating to a cerebral vessel disorder, sleeping disorders, schizophrenia, depression, depression or other symptoms associated with Premenstrual Syndrome (PMS), anxiety and septic shock.
The present salt may also be used where nitric oxide inhibition may also play a role in the treatment, such as pain including somatogenic (either nociceptive or neuropathic), both acute and chronic. The present compounds could be used in any situation that a common NSAID or opioid analgesic would traditionally be administered.
Still, other disorders that may be treated by inhibiting NO production with the present salt include opiate tolerance in patients needing protracted opiate analgesics, and benzodiazepine tolerance in patients taking benzodiazepines, and other addictive behavior, for example, nicotine and eating disorders. The present compounds may also be useful as antibacterial agents.
Further conditions m which the present salt may be used to inhibit NO production from L-argrnlne include systemic hypotension associated with septic and/or toxic shock induced by a wide variety of agents; therapy with cytokiues such as TNF, IL-1 and IL-2; and as an adjuvant to short term rmmunosuppression in transplant therapy.
The present salt"may also be useful in the treatment of an ocular condition (such as ocular hypertension letinitis uveitis)= systemic lupus erythematosis (SLE), glomerulonephtitis., restenosis, inflammalory sequelae of viral infections., acute respiratory distress syndrome (ARDS), oxidant-induced lung injury, JL2 therapy such as in a cancer patient, cachexia, imrnimosuppression such as in transplant therapy, disorders of gastrointestinal motih'ty, sunburn, eczema, psoriasis, gingivitis,, pancreatitis, damage to the gastrointestinal tract resulting from infections, cystic fibrosis treatment to a dysfunctional immune system such as an adjuvant to short term immunostippression in organ transplant therapy, induction of labor, adenomatous polyp osis, controlling tumor growth, chemotherapy, cbemoprevention and bronchitis.
The present invention is also directed to pharmaceutical compositions for the treatment of pain, asthma and other airway disorders, cancer., arthritis, ocular disorders including retinopathies and glaucoma, inflammation related disorders including irritable bowel syndrome, and other disorders in which an excessive production of nitric oxide plays a role, which comprises a therapeutically effective amount ofia crystal of (2S,5Z)-pharmaceutically acceptable carrier., diluent or vehicle.
Besides being useful for human treatment, this form is also useful for veterinary treatment of companion animals, exotic animals and farm animals including mammals birds, and the like. More preferred animals include horses, dogs, and cais.
Brief Description of the Drawings
FIG 1 is a diagram of a unit cell of the 2-ammo-7-(emanimidoylamino)-2-methylhept-5-enoic acid 1.5 HC1 crystalline salt of the present invention;
FIG 2 is a graph of the differential scanning calorimetry study of the 2-amino-7-(ethanimidoylarnino)-2-methylhept-5-enoic acid 1.5 HC1 of the present invention;
FIG 3 is a powder X-ray pattern of 2-arnmo-7-(ethanimidoylamino)-2-methylhept-5-enoic acid 1.5 HC1;
FIG 4 is the calculated X-ray powder pattern from the single crystal structure overlayed with the powder X-ray pattern of 2-amino-7-(ethanimidoylamino)-2-methylhept-5-enoic acid 1.5 HC1;
FIG 5 is a thermogravimetric plot of the -aimno-7-(ethanimidoylamino)-2-methylhept-5-enoic acid 1.5 HC1 of the present invention; and
FIG 6 is the Raman spectrum of the 1.5 HC1 salt of (2S,5Z)-2-amino-7-(ethanimidoylamino)-2-niethylhept-5-enoic acid of the present invention.
Detailed Description of the Invention 1. Definitions
The terms "treat," "treating" and "treatment," as used herein includes prophylactic, palliative treatment, or restorative treatment.
The term "effective amount" means a dose conducive to treatment. An effective amount may be administered in a single dose, or in divided doses over a period of time.
The term "spherulitic" means taking the approximate form of a spherulite.
The term "spherulite" means an ubiquitous form of crystal aggregate, occurring in a wide range of different materials, characterised by radial growth leading to spherical symmetry.
Abbreviations
ACN or alternatively CH3CN is acetom'trile
AcOH is acetic acid
CH2Cl is methyl chloride
DIBAL is diisobutylaluminum hydride
DMF is dimethylformamide
Et3N is triethylamine
EtOAc is ethyl acetate
KHMDS is potassium hexamethyldisilazide
KOH is potassium hydroxide
Mel methyl Iodide
MS is mass spectrum
MsCl is mesylchloride
NaHCO3 is sodium hydrogen carbonate (sodium bicarbonate)
Na2SO4 is sodium sulphate
THF is tetrahydrofuran
Also embraced within this invention is a class of pharmaceutical compositions comprising crystallme(2S,5Z)-2-ammo-7-(emanimidoylamino)-2-methylhept-5-enoic acid hydrochloride in association with one or more non-toxic, pharmaceutically-acceptable carriers and/or diluents and/or adjuvants (collectively referred to herein as "carrier" materials) and, if desired, other active ingredients. The crystalline form of (2S,5Z)-2-ammo-7-(emarumidoylarnino)-2-methylhept-5-enoic acid hydrochloride of the present invention may be administered by any suitable route, preferably in the form of a pharmaceutical composition adapted to such a route, and in a dose effective for the treatment intended. The active (2S,5Z)-2-aminoo-7-(ethanirmdoylarnino)-2-methylhept-5-enoic acid hydrochloride and compositions may, for example, be administered orally, intravascularly, intraperitoneally, subcutaneously, intramuscularly or topically.
For oral administration, the pharmaceutical composition may be in the form of, for example, a tablet, capsule, suspension or liquid. The pharmaceutical composition is preferably made in the form of a dosage unit containing a particular amount of the active ingredient. Examples of such dosage units are tablets or capsules. The active ingredient may also be administered by injection as a composition wherein, for example, saline, dextrose or water may be used as a suitable carrier.
The amount of therapeutically active compound that is administered and the dosage regimen for treating a disease condition with the compound and/or compositions of this invention depends on a variety of factors, including the age, weight, sex and medical condition of the subject, the severity of the disease, the route and frequency of administration, and the particular compound employed, and thus may vary widely. The pharmaceutical compositions may contain active ingredients in the range of about 0.1 to 2000 rug, preferably in the range of about 0.5 to 500 mg and most preferably between
about 1 and 100 mg. A daily dose of about 0.01 to 100mg/kgbody weight, preferably between about 0.5 and about 20 mg/kg body weight and most preferably between about 0.1 to 10 mg/kg body weight, may be appropriate. The daily dose can be administered in one to four doses per day.
Crystalline (2S,5Z)-2-arnino-7-(ethanirnidoylarnino)-2-rnethylhept-5-enoic acid hydrochloride can also be administered by a transdennal device. Preferably topical administration will be accomplished using a patch either of the reservoir and porous membrane type or of a solid matrix variety. In either case, the active agent is delivered continuously from the reservoir or microcapsules through a membrane into the active agent permeable adhesive, which is in contact with the skin or mucosa of the recipient. If the active agent is absorbed through the skin, a controlled and predetermined flow of the active agent is administered to the recipient. In the case of microcapsules, the encapsulating agent may also function as the membrane.
The oily phase of the emulsions of this invention maybe constituted from known ingredients in a known manner. While the phase may comprise merely an emulsifier, it may comprise a mixture of at least one emulsifier with a fat or an oil or with both a fat and an oil. Preferably, a hydrophilic emulsifier is included together with a lipophilic emulsifier which acts as a stabilizer. It is also preferred to include both an oil and a fat. Together, the emulsifier(s) with or without stabilizer(s) make-up the so-called emulsifying wax, and the wax together with the oil and fat make up the so-called emulsifying ointment base which forms the oily dispersed phase of the cream formulations. Emulsifiers and emulsion stabilizers suitable for use in the formulation of the present invention include Tween 60, Span 80, cetostearyl alcohol, myristyl alcohol, glyceryl monostearate, and sodium lauryl sulfate, among others.
The choice of suitable oils or fats for the formulation is based on achieving the desired cosmetic properties, since the solubility of the active compound in most oils likely to be used in pharmaceutical emulsion formulations is very low. Thus, the cream should preferably be a non-greasy, non-staining and washable product with suitable consistency to avoid leakage from tubes or other containers. Straight or branched chain, mono- or dibasic alkyl esters such as di-isoadipate, isocetyl stearate, propylene glycol diester of coconut fatty acids, isopropyl myristate, decyl oleate, isopropyl palmitate, butyl stearate, 2-ethylhexyl palmitate or a blend of branched chain esters maybe used. These
may be used alone or in combination depending on the properties required. Alternatively, high melting point lipids such as white soft paraffin and/or liquid paraffin or other mineral oils can be used.
Formulations suitable for topical administration to the eye also include eye drops wherein the active ingredients are dissolved or suspended in suitable carrier, especially an aqueous solvent for the active ingredients. The anriinflammatory active ingredients are preferably present in such formulations in a concentration of 0-5 to 20%, advantageously 0.5 to 10% and particularly about 1.5% w/w.
For therapeutic purposes, crystalline (2S,5Z)-2-arnino-7-(ethanimidoylamino)-2-methylhept-5-enoic acid hydrochloride is ordinarily combined with one or more adjuvants appropriate to the indicated route of administration. If administered per os, the compound may be admixed with lactose, sucrose, starch powder, cellulose esters of alkanoic acids, cellulose alky] esters, talc, stearic acid, magnesium stearate, magnesium oxide, sodium and calcium salts of phosphoric and sulfuric acids, gelatin, acacia gum, sodium alginate, polyvinylpyrrolidone, and/or polyvinyl alcohol, and then tableted or encapsulated for convenient administration. Such capsules or tablets may contain a controlled-release formulation as maybe provided in a dispersion of active compound in hydroxypropylmethyl cellulose. Formulations for parenteral administration may be in the form of aqueous or non-aqueous isotonic sterile injection solutions or suspensions. These solutions and suspensions may be prepared from sterile powders or granules having one or more of the carriers or diluents mentioned for use in the formulations for oral administration. The crystalline Form B may be dissolved in water, polyethylene glycol, propylene glycol, ethanol, com oil, cottonseed oil, peanut oil, sesame oil, benzyl alcohol, sodium chloride, and/or various buffers. Other adjuvants and modes of administration are well and widely known in the pharmaceutical art.
The amorphous form of (2S,5Z)-2-amino-7-(ethanimidoylamino)-2-methylhept-5-enoic acid hydrochloride may be prepared in accordance with the general scheme shown below:
(Formula Removed)
a) KOH b) Mel c) TBSC1 d) DIBAL e) MsCl f) 3-methyl-l,2,4-oxadiazohn-5-one potassium salt g) AcOH h) Tf2O i) KHMDS / (2S,4S)-3-benzoyl-2-t-butyl-4-methyl-l,3-oxazolidin-5-one j) Lindlar's catalyst k) 6 N HCI
Example 1 - Preparation of (2S,5Z)-2-amino-2-methyl-7-[(l-iminoethyl)amino]-5-heptenoic acid, dihydrochloride:
(Formula Removed)
(2S,5Z)-2-ainino-2-methyl-7-[(l-iminoethyl)amino]-5-heptenoic acid,
dihydrochloride
(Formula Removed)
EX-1A) (Z)-5-t-butyldimethylsi]yloxy-2-penten-l-ol (EX-1A) was prepared from
5,5-dihydro-2-pyrone (Aldrich) by the method of Harold, Mohr and Tamm Helvetica ChimicaActa 66,2,1983 744-754.
(Formula Removed)
EX-IB) To a solution of EX-1A (720 mg, 3.3 mmol) in CH2C12 (25 mL) was added Et3N (525 mg, 5.3 mmol) and methanesulfonyl chloride (561 mg, 4.90 mmol). The reaction mixture was stirred for 15 min at 0°C then at room temperature for 16 h. Additional CH2Cl2 was added, the solution was extracted with NaHCO3, brine and dried to yield 790 mg of a yellow oil. The oil was dissolved in DMF (20 mL) , and (513 mg, 3.7 mmol) was added. The resulting solution was stirred at 50°C for 16 h. The solvent was removed in vacuo and the residue partitioned between EtOAc and brine. The organic layer was dried (Na2SO4) and concentrated to yield an oil which was purified by flash column chromatography on silica gel eluting with ethenhexane (1:1) to give 780 mg g (79%) of the desired protected Z-allylic cyclic amidine product as a clear oil, that contained only the desired Z-isomer by 1HNMR.
(Formula Removed)
EX-1C) A solution of EX-IB (100 mg, 0.34 mmol) in a mixture of acetic acid (1 mL), THF (3 mL) and water (1 mL) was stirred at room temperature for 16 hours. The resulting solution was concentrated in vacua to an oil which was dissolved in EtOAc. The organic layer was washed with saturated NaHCO3, dried (Na2SO4), filtered and evaporated to give 80 mg (quant.) of the desired alcohol product as a clear colorless oil.
(Formula Removed)
EX-ID) To a CH2C12 (3 mL) solution of EX-1C (80 mg, 0.43 mmol) was added Et3N (44 mg) and triflic anhydride (146 mg, 0.52 mmol) at 0 °C, the mixture was stirred for 1.5 h. The solution was concentrated in vacuo. and To the resulting yellow slurry was added a CH2C12 (1-5 mL) solution of EX-2D (0.15 g, 0.74 mmol). The crude material was purified by flash column chromatography on silica gel eluting with EtOAc:hexane (1:1) to give 62 mg (44%) of the desired triflate product as a clear oil.
(Formula Removed)
EX-IE) To a THF (10 mL) solution of (2S,4S)-3-benzoyl-2-t-butyl-4-methyl-l,3-oxazolidin-5-one (Ref.) (532 mg, 2.04 mmol) at -78oC was added KHMDS (4.48 mL, 2.2 mmol, 0.5 M in THF). The resulting orange colored solution was stirred for 15 min. followed by the addition of EX-ID (580 mg, 1.8 mmol). The resulting solution was allowed to warm to room temperature followed by the addition of KHSO4 (10%, 1.5 mL)
brine and EtOAc. The organic layer was separated, dried and concentrated in vacuo to yield 960 mg of a yellow oil. The crude material was purified by flash column chromatography on silica gel eluting with EtOAc:hexane (1:1) to give 138 mg (18%) of the desired alkylated product as a clear oil.
(Formula Removed)
EX-1) To a methanol (10 mL) solution of EX-IE (138 mg, 0.32 mmol) was added
Lindlar catalyst (260 mg). The stirred slurry was refluxed for 2 hours, then cooled to
room temperature. The catalyst was removed by filtration through celite, and the filtrate
was stripped to give the desired deprotected amidine product as a pale yellow oil. A
solution of the yellow oil in HCI (6N, 10 mL) was refluxed for 1.75 hours. The solvent
was removed in vacuo, and the resulting foam was purified by reverse-phase HPLC
eluting with a 30 minute gradient of 0-40% CH3CN/H2O(0.25% acetic acid). Fractions
containing product were combined and concentrated to a foam. The product was
dissolved in 1 N HCI and the solvent removed in vacuo (2x) to give 34 mg (20%) of the
desired (2iS',5Z)-2-amino-2-methyl-7-[(l-iminoethyl)animo]-5-heptenoic acid,
dihydrochloride product. MS calcd. for C10H19N3O2: m/z = 214 [M+H]+, found: 214. (100 %) 1H NMR (D20) δ 1.40 (s, 3H), 1.5-2.0 (m, 4H) 1.90 (s, 3H), 3.55 (m, 2H) 5.15-5.25 (m, vinyl, 1H), 5.30-5.45 (m, vinyl, 1H).
Table I: Analysis
(Table Removed)
Example 2 - preparation of the crystal form of (2S,5Z)-2-amino-7-(ethanimidoylamino)-2-methylhept-5-enoic acid
Crystallization
Amorphate (2S,5Z)-2-ammo-7-(etoanimidoylammo)-2-methylhept-5-enoic acid, with excess hydrochloride, is freely soluble in water, methanol and ethanol, and soluble in isopropanol and various solvents containing water such as 10% water in THF, water saturated ethyl acetate, 10% water in acetonitrile and higher alcohols with water. The amorphate is insoluble at significantly less than one mg/mL in the dry solvents tested: acetone, MEK, methyl isobutyl ketone, THF, ethyl acetate, chloroform, methylene chloride, hexanes, cylcohexane, di-isopropyl ether, acetonitrile and toluene.
About 460 mg of (2S,5Z)-2-ammo-7-(ethaninaidoylarnino)-2-methylhept-5-enoic acid was dissolved in 10 mL of HPLC grade water. Amberlite IRA400 ion exchange resin that had been converted from the chloride form to the hydroxide form was used to titrate the solution of (2S,5Z)-2-arnmo-7-(emaaimidoylamino)-2-methylhept-5-enoic acid to pH 10.7. A chloride selective electrode indicated chloride was reduced to 200 ppm. This solution was filtered through a Milh'pore 5 µm LS membrane and the solution was lyophih'zed. Elemental analysis of the freeze dried solid, Table n, indicated chloride was reduced to 0.25 equivalents, which was consistent with the 200 ppm ion selective electrode reading.
Table II
Elemental analysis results: measured by combustion analysis vs. theory, weight percent.

(Table Removed)
Hydrochloride salt, (2S,5Z)-2-ammo-7-(ethanimidoylarnrno)-2-methylhept-5-enoic acid was dissolved in water, various low alcohols, THF-water, acetonitrile-water and water saturated ethyl acetate to obtain concentrated solutions. The antisolvents listed above were used to force the salt from solution. Liquid - liquid phase outs, emulsions and glassy precipitates were obtained in all cases. Vapor diffusion cells were also set up with a few systems as well, producing exclusively emulsion phase outs.
A sample of hydrochloride salt was rotary evaporated, dissolved, lyophilized and allowed to stand for four to six weeks in a fume hood. This sample began to spontaneously change. Polarized light microscopy was used to show that crystallization was occurring. Nearly half of the volume of sample became discolored and never did crystallize, but nearly half did crystallize. Some of the material was used as seeds in a number of crystallization experiments, with various solvents, to obtain more crystalline material from (2S,5Z)-2-ammo-7-(emanimidoylamino)-2-methylhept-5-enoic acid hydrochloride. Very little if any crystallization occurred and then only very slowly. Crystals from each lot were examined by polarized light microscopy for evidence of polymorphism. The crystal habit and optical properties remained consistent to one form. Crystals from each lot were biaxial, exhibited a face of high birefringence and a face of low birefringence n1-n2 No evidence of solvation was noted by Scanning electron microscopy with energy dispersive spectroscopy SEM/EDS or hot stage polarized light microscopy. The eutectic melt of the crystals; with the discolored oily phase which could not be completely removed without also dissolving the crystals; was about 210 °C.
Several large crystals were isolated from a first sample for structural determination. The stoichiometry of the unit cell was determined to be: two independent
molecules of (2S,5Z)-2-arnmo-7-(ethanirrudoylarnino)-2-methylhept-5-enoic acid and three HCl's. No solvation was observed. The space group was PI (triclinic) and the unit cell a = 8.1623, b = 9.0524, c = 10.5937, alpha = 71.522, beta = 73.472, gamma = 86.086. The absolute configuration of 2-amino-7-(e1nammidoylainino)-2-methylhept-5-enoic acid was confirmed to be "S".
About 1.5 g of (2S,5Z)-2-aniino-7-(ethanimidoylamino)-2-niethylhept-5-enoic acid, (2.5 HC1 x 2.0 H2O) was dissolved in 5.0 ml H2O and amberlite OH resin was added to titrate to pH 7, as measured with a pH electrode and meter. The solution was filtered through a 5 µm LS Millipore filter and lyophilized to yield 903 mg of the monohydrochloride salt. The lyophilized material was virtually dissolved in 6.0 mL of isopropanol containing 0.38% H2O followed by the addition of HC1 (150 µL, 12 M) to form the sesquihydrochloride. This mixture was vortexed and sonicated then allowed to stir overnight at room temperature to ensure saturation and equilibrium. Seed crystals were then added (about 0.1 mg) and stirring continued. Crystallization was noted to begin within minutes and appeared to be substantial within 3 hours. The solution was stirred at room temperature for 48 hours. The crystals were collected by filtration, washed with a small volume of isopropanol and vacuum dried at 40 °C overnight to yield 860 mg, 89% of theory, of white solid.
It will be appreciated that "seeding" a solution of (2S,5Z)-2-amino-7-(ethanimidoylamino)-2-methylhept-5-enoic acid may initiate or increase nucleation under the described conditions. Crystals are available from Pharmacia Corporation, 4901 Searle Parkway, Skokie, Illinois, USA 60077.
Two similar experiments were conducted. A few hundred milligrams of (2S,5Z)-2-aimino-7-(emammidoylamino)-2-methylhept-5-enoic acid were dissolved to approximately the same concentration in isopropanol as the lyophilized material in the previous experiment. The hydrochloride concentration was not adjusted. This system was seeded and stirred at ambient temperature. No crystallization was observed. In the next experiment the pH of the solution was adjusted with concentrated sodium hydroxide to about pH 3 and seeded. Some crystalline product was obtained, but the yield was only about 30 to 40%. Addition of ether increased the yield to near 90%.
Examples - Characterization of (2S,5Z)-2-amino-7-(ethanimidovlamino)-2-methylhept-5-enoic acid Crystalline Salt
The solid 2-amino-7-(ethanimidoylamino)-2-methylhept-5-enoic acid 1.5HCI was crystalline by polarized light microscopy and the crystallite size was on the order of one micrometer. The agglomerated particles were spherulitic. Elemental analysis of 2-ammo-7-(ethanimidoyIamino)-2-methylhept-5-enoic acid 1.5 HCI by physical methodology provided a very tight correspondence with theory for a 1.5 HCI salt with no solvation, see Table HI. Coulometric Karl Fischer water analysis found 0.6% water, 0.09 equivalents, from an average of two measurements.
Table III
Elemental analysis results of 2-amino-7-(emanimidoylamino)-2-methylhept-5-enoic acid
1.5 HCI Measured by combustion analysis vs. theory; weight percent.
(Table Removed)
Polarized light microscopy of (2S,5Z)-2-amino-7-ethaniniidoylamino)-2-methylhept-5-enoic acid 1.5 HCI found refractive indices nd α 1.508, ß approximately 1.59, γ 1.608, a negative optic sign and 2V near 37 degrees. Strong dispersion of the optic axes were apparent in the interference figures.
Differential scanning calorimetry (DSC) found a single melt at 224 °C and a heat of fusion of 147 joules gram-1. (See Fig. 2).
Fig. 3 shows the powder x-ray pattern of 2-ammo-7-(ethanirnidoylamino)-2-methylhept-5-enoic acid 1.5 HCI.
Referring to Fig. 4, the calculated x-ray powder pattern from the single crystal structure overlayed with the powder x-ray pattern of 2-ammo-7-(emanimidoylamino)-2-methylhept-5-enoic acid 1.5 HCI agree very well, with allowance for the temperature difference. The single crystal data was collected at 120 °K and the powder x-ray data at ambient.
No mass loss was observed by thermogravimetric analysis (TGA) to the initiation of melt (see Fig 5). A loss of 0.47% was noted during melting by TGA.
The crystalline 2-amino-7-(ethanimidoylamino)-2-methylhept-5-enoic acid 1.5 HC1 is nonhygroscopic at and below 70% relative humidity. Moisture sorption of 2-amino-7-(ethanirnidoylamino)-2-methylhept-5-enoic acid 1.5 HC1 at 25 °C, by DVS moisture balance, showed a moisture gain of 0.91% at 70% relative humidity (R.H.). At 80% R.H. the gain was 18.5%, and at 90% R.H. the gain was 76.8%. The instrument cycled back to low relative humidity and the sample was removed then examined by polarized light microscopy. The sample was fully crystalline after removal from the moisture balance, but the crystallite size had increased. The easily observed optical properties by PLM suggested that no change in crystal form occurred, but at least some of the sample had deliquesced and recrystallized on drying, Table IV shows the detailed data from the DVS moisture balance. This salt form, 1.5 HC1 has no solvation.
Table IV
(Table Removed)






WE CLAIM:
1. A crystal form of (2S, 5Z)-2-amino-7-(ethanirnidoylamino)-2-
methylhept-5-enoic acid and pharmaceutically acceptable salts thereof.
2. A compound of formula (I) as claimed in claim 1
(Formula Removed)
being (2S,5Z)-2-amino-7-(ethanimidoylamino)-2-methylhept-5-enoic acid, 1.5 hydrochloride or a physiologically functional derivative thereof.
3. A pharmaceutical composition comprising an effective amount of
(2S, 5Z)-2-amino-7-(ethanimidoylamino)-2-methylhept-5-enoic acid, 1.5
hydrochloride as claimed in claim 2, together with a pharmaceutically
acceptable carrier.
4. A process of making crystalline (2S, 5Z)-2-amino-7-
(ethanimidoylamino)-2-methylhept-5-enoic acid:

(a) Obtaining a non-crystalline form of (2S, 5Z)-2-amino-7-
(ethanimidoylamino)-2-methylhept-5-enoic acid;
(b) adding hydrochloric acid until the (2S, 5Z)-2-amino-7-
(ethanimidoylamino)-2-methylhept-5-enoic acid acid reaches 1.5 HCI
equivalents;
(c) adjusting hydrochloric acid concentration with an appropriate
base until the ((2S, 5Z)-2-amino-7-(ethanimidoylamino)-2-methylhept-
5-enoic acid reaches 1.5 HCI equivalents;
(d) removing any other salt counterion from the (2S, 5Z)-2-amino-7-
(ethanimidoylamino)-2-methylhept-5-enoic acid and adding
hydrochloric acid until the (2S, 5Z)-2-amino-7-(ethanimidoylamino)-2-
methylhept-5-enoic acid acid reaches 1.5 hydrochloride equivalents;
(e) seeding the (2S, 5Z)-2-amino-7-(ethanimidoylamino)-2-
methylhept-5-enoic acid, 1.5 hydrochloride obtained with crystalline
(2S, 5Z)-2-amino-7-(ethanimidoylamino)-2-methylhept-5-enoic acid, 1.5
hydrochloride; and


Documents:

384-delnp-2005-abstract.pdf

384-delnp-2005-assignment.pdf

384-delnp-2005-claims.pdf

384-delnp-2005-complete specification (as filed).pdf

384-delnp-2005-complete specification (granted).pdf

384-delnp-2005-correspondence-others.pdf

384-delnp-2005-correspondence-po.pdf

384-delnp-2005-description (complete).pdf

384-delnp-2005-drawings.pdf

384-delnp-2005-form-1.pdf

384-delnp-2005-form-18.pdf

384-delnp-2005-form-2.pdf

384-delnp-2005-form-3.pdf

384-delnp-2005-form-5.pdf

384-delnp-2005-gpa.pdf

384-delnp-2005-pct-210.pdf

384-delnp-2005-pct-304.pdf

384-delnp-2005-pct-402.pdf

384-delnp-2005-pct-409.pdf

384-delnp-2005-pct-416.pdf

384-delnp-2005-petition-137.pdf

384-delnp-2005-petition-138.pdf


Patent Number 247768
Indian Patent Application Number 384/DELNP/2005
PG Journal Number 20/2011
Publication Date 20-May-2011
Grant Date 16-May-2011
Date of Filing 02-Feb-2005
Name of Patentee PHARMACIA CORPORATION
Applicant Address 700 CHESTERFIED PARKWAY WEST, CHESTERFIELD, MISSOURI 63017-1732, U.S.A.
Inventors:
# Inventor's Name Inventor's Address
1 ANN E. HALLINAN 135 BARTON AVENUE, EVANSTON, IL 60202, U.S.A.
PCT International Classification Number C07C 257/14
PCT International Application Number PCT/US2003/026347
PCT International Filing date 2003-08-22
PCT Conventions:
# PCT Application Number Date of Convention Priority Country
1 60/405,526 2002-08-23 U.S.A.