NZ614787B2 - Crystalline forms and processes for the preparation of condensed azacycles ( cannabinoid receptor modulators) - Google Patents
Crystalline forms and processes for the preparation of condensed azacycles ( cannabinoid receptor modulators) Download PDFInfo
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- NZ614787B2 NZ614787B2 NZ614787A NZ61478712A NZ614787B2 NZ 614787 B2 NZ614787 B2 NZ 614787B2 NZ 614787 A NZ614787 A NZ 614787A NZ 61478712 A NZ61478712 A NZ 61478712A NZ 614787 B2 NZ614787 B2 NZ 614787B2
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- New Zealand
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- crystalline form
- cyclopropa
- diaza
- tetrahydro
- hydroxymethyl
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Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/4965—Non-condensed pyrazines
- A61K31/497—Non-condensed pyrazines containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/13—Crystalline forms, e.g. polymorphs
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
Abstract
Disclosed are anhydrous crystalline forms of condensed azacycles with pyrazole and pyrazine components, and a process for preparing the compounds by crystallising from acetonitrile and water, and other non-selective solvates. The anhydrous crystalline form of (1aS,5aS)-2-(4-oxy-pyrazin-2-yl)-1a,2,5.5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalene-4-carboxylic acid ((S)-1 -hydroxymethyl-2,2-dimethyl-propyl)-amide (Compound 1) and pharmaceutical compositions thereof are disclosed which modulate the activity of the cannabinoid CB receptor and are therefore useful in the treatment of CB receptor-mediated disorders, for example, osteoarthritis; pain; hyperalgesia; allodynia; inflammatory hyperalgesia; neuropathic hyperalgesia; acute nociception; osteoporosis; multiple sclerosis-associated spasticity; autoimmune disorders; allergic reactions CNS inflammation for example; atherosclerosis; undesired immune cell activity, and inflammation associated with a disorder selected from: osteoarthritis, anaphylaxis, Behcet's disease, graft rejection, vasculitis, gout, spondylitis, viral disease, bacterial disease, lupus, inflammatory bowel disease, autoimmune hepatitis, and type 1 diabetes mellitus; age-related macular degeneration; cough; leukaemia; lymphoma; CNS rumours; prostate cancer; Alzheimer's disease; stroke-induced damage; dementia; amyotrophic lateral sclerosis; and Parkinson's disease. 5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalene-4-carboxylic acid ((S)-1 -hydroxymethyl-2,2-dimethyl-propyl)-amide (Compound 1) and pharmaceutical compositions thereof are disclosed which modulate the activity of the cannabinoid CB receptor and are therefore useful in the treatment of CB receptor-mediated disorders, for example, osteoarthritis; pain; hyperalgesia; allodynia; inflammatory hyperalgesia; neuropathic hyperalgesia; acute nociception; osteoporosis; multiple sclerosis-associated spasticity; autoimmune disorders; allergic reactions CNS inflammation for example; atherosclerosis; undesired immune cell activity, and inflammation associated with a disorder selected from: osteoarthritis, anaphylaxis, Behcet's disease, graft rejection, vasculitis, gout, spondylitis, viral disease, bacterial disease, lupus, inflammatory bowel disease, autoimmune hepatitis, and type 1 diabetes mellitus; age-related macular degeneration; cough; leukaemia; lymphoma; CNS rumours; prostate cancer; Alzheimer's disease; stroke-induced damage; dementia; amyotrophic lateral sclerosis; and Parkinson's disease.
Description
FORMS AND PROCESSES FOR THE PREPARATION OF CANNABINOID
RECEPTOR MODULATORS
FIELD OF THE INVENTION
The present invention relates to crystalline forms of (1aS,5aS)(4-oxy-pyrazinyl)-
1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S)
hydroxymethyl-2,2-dimethyl-propyl)-amide (Compound 1) and pharmaceutical compositions
thereof that modulate the activity of the cannabinoid CB receptor and are therefore useful in the
treatment of CB receptor-mediated disorders, for example, osteoarthritis; pain, for example
bone and joint pain, muscle pain, dental pain, migraine and other headache pain, inflammatory
pain, neuropathic pain, pain that occurs as an adverse effect of therapeutics, and pain associated
with a disorder selected from: osteoarthritis, cancer, multiple sclerosis, allergic reactions,
nephritic syndrome, scleroderma, thyroiditis, diabetic neuropathy, fibromyalgia, HIV related-
neuropathy, sciatica, and autoimmune conditions; hyperalgesia; allodynia; inflammatory
hyperalgesia; neuropathic hyperalgesia; acute nociception; osteoporosis; multiple sclerosis-
associated spasticity; autoimmune disorders, for example an autoimmune disorder selected from
the group consisting of: multiple sclerosis, Guillan-Barré syndrome, polyradiculoneuropathy,
chronic inflammatory demyelination, rheumatoid arthritis, psoriatic arthritis, ankylosing
spondylarthritis, and reactive arthritis; allergic reactions, for example, an allergic reaction
associated with a disorder selected from: atopic dermatitis, pruritis, urticaria, asthma,
conjunctivitis, allergic rhinitis, and anaphylaxis; CNS inflammation for example, CNS
inflammation associated with a disorder selected from: Alzheimer's disease, stroke, dementia,
amyotrophic lateral sclerosis, and human immunodeficiency virus; atherosclerosis; undesired
immune cell activity, and inflammation associated with a disorder selected from: osteoarthritis,
anaphylaxis, Behcet's disease, graft rejection, vasculitis, gout, spondylitis, viral disease,
bacterial disease, lupus, inflammatory bowel disease, autoimmune hepatitis, and type 1 diabetes
mellitus; age-related macular degeneration; cough; leukemia; lymphoma; CNS tumors; prostate
cancer; Alzheimer's disease; stroke-induced damage; dementia; amyotrophic lateral sclerosis,
and Parkinson's disease. The present invention further relates to processes and intermediates
useful in the preparation crystalline forms and solvates of Compound 1 and pharmaceutical
compositions thereof.
BACKGROUND OF THE INVENTION
Cannabinoids are a group of extracellular signaling molecules that are found in both
plants and animals. Signals from these molecules are mediated in animals by two G-protein
coupled receptors, Cannabinoid Receptor 1 (CB ) and Cannabinoid Receptor 2 (CB ). CB is
1 2 1
expressed most abundantly in the neurons of the CNS but is also present at lower concentrations
in a variety of peripheral tissues and cells (Matsuda, L. A. et al. (1990) Nature 346:561-
564). In contrast, CB is expressed predominantly, although not exclusively, in non-neural
tissues, e.g. in hematopoietic cells, endothelial cells, osteoblasts, osteoclasts, the endocrine
pancreas, and cancerous cell lines (Munro, S. et al. (1993) Nature 365:61-65; and as reviewed in
Pacher, P. et al. (2006) Pharmacol. Rev. 58(3): 389-462). As such, CB is believed to be
primarily responsible for mediating the psychotropic effects of cannabinoids on the body,
whereas CB is believed to be primarily responsible for most of their non-neural effects.
SUMMARY OF THE INVENTION
One aspect of the present invention relates to crystalline forms of (1aS,5aS)(4-oxy-
pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S)-
1-hydroxymethyl-2,2-dimethyl-propyl)-amide (Compound 1):
One aspect of the present invention relates to an anhydrous crystalline form of
(1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalene
carboxylic acid ((S)hydroxymethyl-2,2-dimethyl-propyl)-amide (Compound 1).
One aspect of the present invention relates to processes for preparing an anhydrous
crystalline form of (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-
cyclopropa[a]pentalenecarboxylic acid ((S)hydroxymethyl-2,2-dimethyl-propyl)-amide
comprising the steps of:
1) crystallizing (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-
2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S)hydroxymethyl-2,2-
dimethyl-propyl)-amide from a crystallizing mixture to obtain a crystalline form of
(1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-
cyclopropa[a]pentalenecarboxylic acid ((S)hydroxymethyl-2,2-dimethyl-propyl)-
amide in the crystallizing mixture, wherein the crystallizing mixture comprises
acetonitrile and water; and
2) isolating the crystalline form of (1aS,5aS)(4-oxy-pyrazinyl)-
1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S)
hydroxymethyl-2,2-dimethyl-propyl)-amide from the crystallizing mixture to obtain the
anhydrous crystalline form of (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-
1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S)hydroxymethyl-2,2-
dimethyl-propyl)-amide.
One aspect of the present invention relates to an anhydrous crystalline form of
(1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalene
carboxylic acid ((S)hydroxymethyl-2,2-dimethyl-propyl)-amide prepared by a process as
described herein.
One aspect of the present invention relates to compositions comprising an anhydrous
crystalline form of (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-
cyclopropa[a]pentalenecarboxylic acid ((S)hydroxymethyl-2,2-dimethyl-propyl)-amide as
described herein.
One aspect of the present invention relates to compositions comprising an anhydrous
crystalline form of (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-
cyclopropa[a]pentalenecarboxylic acid ((S)hydroxymethyl-2,2-dimethyl-propyl)-amide as
described herein, and a pharmaceutically acceptable carrier.
One aspect of the present invention relates to processes of making a composition
comprising mixing an anhydrous crystalline form of (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-
tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S)hydroxymethyl-2,2-
dimethyl-propyl)-amide as described herein, with a phamaceutically acceptable carrier.
One aspect of the present invention relates to methods for the treatment of a
cannabinoid receptor-mediated disorder in an individual, comprising administering to the
individual in need thereof, a therapeutically effective amount of an anhydrous crystalline form
of (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalene-
4-carboxylic acid ((S)hydroxymethyl-2,2-dimethyl-propyl)-amide as described herein or a
pharmaceutical composition thereof.
One aspect of the present invention relates to methods for the treatment of a CB
receptor-mediated disorder in an individual, comprising administering to the individual in need
thereof, a therapeutically effective amount of an anhydrous crystalline form of (1aS,5aS)(4-
oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid
((S)hydroxymethyl-2,2-dimethyl-propyl)-amide as described herein or a pharmaceutical
composition thereof.
One aspect of the present invention relates to the use of an anhydrous crystalline form of
(1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalene
carboxylic acid ((S)hydroxymethyl-2,2-dimethyl-propyl)-amide as described herein, in the
manufacture of a medicament for the treatment of a cannabinoid receptor-mediated disorder.
One aspect of the present invention relates to the use of an anhydrous crystalline form of
(1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalene
carboxylic acid ((S)hydroxymethyl-2,2-dimethyl-propyl)-amide as described herein, in the
manufacture of a medicament for the treatment of a CB receptor-mediated disorder.
One aspect of the present invention relates to an anhydrous crystalline form of
(1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalene
carboxylic acid ((S)hydroxymethyl-2,2-dimethyl-propyl)-amide as described herein, for use
in a method of treatment of the human or animal body by therapy.
One aspect of the present invention relates to an anhydrous crystalline form of
(1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalene
carboxylic acid ((S)hydroxymethyl-2,2-dimethyl-propyl)-amide as described herein, for use
in a method of treatment of a cannabinoid receptor-mediated disorder.
One aspect of the present invention relates to an anhydrous crystalline form of
(1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalene
carboxylic acid ((S)hydroxymethyl-2,2-dimethyl-propyl)-amide as described herein, for use
in a method of treatment of a CB receptor-mediated disorder.
One aspect of the present invention relates to acetone solvates of (1aS,5aS)(4-oxy-
pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S)-
1-hydroxymethyl-2,2-dimethyl-propyl)-amide.
One aspect of the present invention relates to non-selective solvates of (1aS,5aS)(4-
oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid
((S)hydroxymethyl-2,2-dimethyl-propyl)-amide.
One aspect of the present invention relates to ethyl acetate solvates of (1aS,5aS)(4-
oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid
((S)hydroxymethyl-2,2-dimethyl-propyl)-amide.
Certain modulators of the cannabinoid receptor are described in PCT application
, filed 27 August 2010 (International Publication Number
WO2011/025541), and in United States provisional applications 61/275,506, 61/396,588, and
61/400,146, each of which is incorporated herein by reference in its entirety.
These and other aspects of the invention disclosed herein will be set forth in greater
detail as the patent disclosure proceeds.
BRIEF DESCRIPTION OF THE DRAWINGS
Figure 1 shows a differential scanning calorimetry (DSC) thermogram for a sample
containing a crystalline form of Compound 1 (CH Cl solvate) and a thermogravimetric analysis
(TGA) thermogram of a sample containing a crystalline form of Compound 1 (CH Cl solvate).
Figure 2 shows an overlay of a powder X-ray diffraction (PXRD) pattern for a sample
containing a crystalline form of Compound 1 (CH Cl solvate) obtained from recrystallization
using CH Cl /hexane (Top Trace) and a powder X-ray diffraction (PXRD) pattern for a sample
containing a crystalline form of Compound 1 (CH Cl solvate) obtained by slurrying non-
solvated Compound 1 in CH Cl (Bottom Trace). The PXRD showed the crystalline solvate
obtained from the CH Cl slurry is substantially indistinguishable from the crystalline solvate
resulting from CH Cl /hexane recrystallization.
Figure 3 shows the asymmetric unit for the hemi-CH Cl solvate of Compound 1 based
on single-crystal X-ray diffraction analysis.
Figure 4 shows a powder X-ray diffraction (PXRD) pattern for a sample containing an
anhydrous crystalline form of Compound 1.
Figure 5 shows a differential scanning calorimetry (DSC) thermogram for a sample
containing anhydrous crystalline form of Compound 1 and a thermogravimetric analysis (TGA)
thermogram of a sample containing anhydrous crystalline form of Compound 1.
Figure 6 shows a powder X-ray diffraction (PXRD) pattern for a sample containing an
anhydrous crystalline form of Compound 1.
Figure 7 shows a differential scanning calorimetry (DSC) thermogram for a sample
containing anhydrous crystalline form of Compound 1 and a thermogravimetric analysis (TGA)
thermogram of a sample containing anhydrous crystalline form of Compound 1.
Figure 7A shows an adsorption and desorption isotherm, Dyanmic Moisture Sorption
(DMS), for a sample containing anhydrous crystalline form of Compound 1.
Figure 8 shows a powder X-ray diffraction (PXRD) pattern for a sample containing a
crystalline form of Compound 1 (acetone solvate).
Figure 9 shows a differential scanning calorimetry (DSC) thermogram for a sample
containing a crystalline form of Compound 1 (acetone solvate) and a thermogravimetric analysis
(TGA) thermogram of a sample containing a crystalline form of Compound 1 (acetone solvate).
Figure 10 shows a powder X-ray diffraction (PXRD) pattern for a sample containing a
crystalline form of Compound 1 (non-selective solvate), see Example 6.
Figure 11 shows a powder X-ray diffraction (PXRD) pattern for a sample containing a
crystalline form of Compound 1 (non-selective solvate), see Example 6.
Figure 12 shows a powder X-ray diffraction (PXRD) pattern for a sample containing a
crystalline form of Compound 1 (non-selective solvate), see Example 6.
Figure 13 shows a differential scanning calorimetry (DSC) thermogram for a sample
containing a crystalline form of Compound 1 (non-selective solvate) and a thermogravimetric
analysis (TGA) thermogram of a sample containing a crystalline form of Compound 1 (non-
selective solvate), see Example 6.
Figure 14 shows a differential scanning calorimetry (DSC) thermogram for a sample
containing a crystalline form of Compound 1 (non-selective solvate) and a thermogravimetric
analysis (TGA) thermogram of a sample containing a crystalline form of Compound 1 (non-
selective solvate), see Example 6.
Figure 15 shows a differential scanning calorimetry (DSC) thermogram for a sample
containing a crystalline form of Compound 1 (non-selective solvate) and a thermogravimetric
analysis (TGA) thermogram of a sample containing a crystalline form of Compound 1 (non-
selective solvate), see Example 6.
Figure 16 shows a powder X-ray diffraction (PXRD) pattern for a sample containing a
crystalline form of Compound 1 (ethyl acetate solvate).
Figure 17 shows a differential scanning calorimetry (DSC) thermogram for a sample
containing a crystalline form of Compound 1 (ethyl acetate solvate) and a thermogravimetric
analysis (TGA) thermogram of a sample containing a crystalline form of Compound 1 (ethyl
acetate solvate).
Figure 18 shows the effect of Compound 1 in the monosodium iodoacetate (MIA)
model of osteoarthritis in rats, see Example 9.
DETAILED DESCRIPTION OF THE INVENTION
DEFINITIONS
For clarity and consistency, the following definitions will be used throughout this patent
document.
Throughout this specification the word "comprise", or variations such as "comprises" or
"comprising", will be understood to imply the inclusion of a stated element, integer or step, or
group of elements, integers or steps, but not the exclusion of any other element, integer or step,
or group of elements, integers or steps.
The term “agonist” refers to a moiety that interacts with and activates a G-protein-
coupled receptor, for instance a cannabinoid receptor, and can thereby initiate a physiological or
pharmacological response characteristic of that receptor. For example, an agonist may activate
an intracellular response upon binding to a receptor, or enhance GTP binding to a membrane.
The term "in need of treatment" and the term "in need thereof" when referring to
treatment are used interchangeably to mean a judgment made by a caregiver (e.g. physician,
nurse, nurse practitioner, etc. in the case of humans; veterinarian in the case of animals,
including non-human mammals) that an individual or animal requires or will benefit from
treatment. This judgment is made based on a variety of factors that are in the realm of a
caregiver’s expertise, but that includes the knowledge that the individual or animal is ill, or will
become ill, as the result of a disease, condition or disorder that is treatable by the compounds of
the invention. Accordingly, the compounds of the invention can be used in a protective or
preventive manner; or compounds of the invention can be used to alleviate, inhibit or ameliorate
the disease, condition or disorder.
The term “individual” refers to any animal, including mammals, preferably mice, rats,
other rodents, rabbits, dogs, cats, swine, cattle, sheep, horses, or primates, and most preferably
humans.
The term “modulate or modulating” refers to an increase or decrease in the amount,
quality, response or effect of a particular activity, function or molecule.
The term “composition” refers to a compound or crystalline form thereof, including but
not limited to, salts, solvates, and hydrates of a compound of the present invention, in
combination with at least one additional component, such as, a composition obtained/prepared
during synthesis, preformulation, in-process testing (i.e., TLC, HPLC, NMR samples), and the
like
The term “pharmaceutical composition” refers to a specific composition comprising at
least one active ingredient; including but not limited to, salts, solvates, and hydrates of
compounds of the present invention, whereby the composition is amenable to investigation for a
specified, efficacious outcome in a mammal (for example, without limitation, a human). Those
of ordinary skill in the art will understand and appreciate the techniques appropriate for
determining whether an active ingredient has a desired efficacious outcome based upon the
needs of the artisan.
The term “therapeutically effective amount” refers to the amount of active compound or
pharmaceutical agent that elicits the biological or medicinal response in a tissue, system, animal,
individual or human that is being sought by a researcher, veterinarian, medical doctor or other
clinician or caregiver or by an individual, which includes one or more of the following:
(1) Preventing the disease, for example, preventing a disease, condition or disorder in an
individual that may be predisposed to the disease, condition or disorder but does not yet
experience or display the pathology or symptomatology of the disease;
(2) Inhibiting the disease, for example, inhibiting a disease, condition or disorder in an
individual that is experiencing or displaying the pathology or symptomatology of the disease,
condition or disorder (i.e., arresting further development of the pathology and/or
symptomatology); and
(3) Ameliorating the disease, for example, ameliorating a disease, condition or disorder
in an individual that is experiencing or displaying the pathology or symptomatology of the
disease, condition or disorder (i.e., reversing the pathology and/or symptomatology).
It is appreciated that certain features of the invention, which are, for clarity, described in
the context of separate embodiments, may also be provided in combination in a single
embodiment. Conversely, various features of the invention, which are, for brevity, described in
the context of a single embodiment, may also be provided separately or in any suitable
subcombination. In addition, subcombinations of uses and medical indications listed in the
embodiments describing such uses and medical indications described herein, are also
specifically embraced by the present invention just as if each and every subcombination of uses
and medical indications was individually and explicitly recited herein.
PROCESSES OF THE INVENTION
The present invention is directed to, inter alia, processes useful in the preparation of an
anhydrous crystalline form of (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-
diaza-cyclopropa[a]pentalenecarboxylic acid ((S)hydroxymethyl-2,2-dimethyl-propyl)-
amide, a modulator of the cannabinoid CB receptor.
One aspect of the present invention relates to processes for preparing an anhydrous
crystalline form of (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-
cyclopropa[a]pentalenecarboxylic acid ((S)hydroxymethyl-2,2-dimethyl-propyl)-amide
comprising the steps of:
1) crystallizing (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-
2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S)hydroxymethyl-2,2-
dimethyl-propyl)-amide from a crystallizing mixture to obtain a crystalline form of
(1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-
cyclopropa[a]pentalenecarboxylic acid ((S)hydroxymethyl-2,2-dimethyl-propyl)-
amide in the crystallizing mixture, wherein the crystallizing mixture comprises
acetonitrile and water; and
2) isolating the crystalline form of (1aS,5aS)(4-oxy-pyrazinyl)-
1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S)
hydroxymethyl-2,2-dimethyl-propyl)-amide from the crystallizing mixture to obtain the
anhydrous crystalline form of (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-
1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S)hydroxymethyl-2,2-
dimethyl-propyl)-amide.
In some embodiments, crystallizing is conducted at a temperature of about -10 °C to
about 35 °C. In some embodiments, crystallizing is conducted at a temperature of about -10 °C
to about 25 °C. In some embodiments, crystallizing is conducted at a temperature of about -10
°C to about 10 °C. In some embodiments, crystallizing is conducted at a temperature of about -5
°C to about 5 °C.
In some embodiments, the crystallizing mixture is prepared by the steps of:
1) dissolving (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-
cyclopropa[a]pentalenecarboxylic acid ((S)hydroxymethyl-2,2-dimethyl-propyl)-amide in
acetonitrile and a first amount of water to form a first mixture; and
2) adding a second amount of water to the first mixture to obtain the crystallizing
mixture. In some embodiments, dissolving is conducted at a temperature of about 25 °C to about
80 °C. In some embodiments, dissolving is conducted at a temperature of about 40 °C to about
70 °C. In some embodiments, dissolving is conducted at a temperature of about 55 °C to about
65 °C. In some embodiments, dissolving is conducted at a temperature of about 58 °C to about
62 °C. In some embodiments, dissolving is conducted at a temperature of about 60 °C. In some
embodiments, the molar ratio present in the first mixture between (1aS,5aS)(4-oxy-pyrazin
yl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S)
hydroxymethyl-2,2-dimethyl-propyl)-amide, acetonitrile, and first amount water is about
1.0:7.3:30.0 to about 1.0:12.1:49.6. In some embodiments, the molar ratio present in the first
mixture between (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-
cyclopropa[a]pentalenecarboxylic acid ((S)hydroxymethyl-2,2-dimethyl-propyl)-amide,
acetonitrile, and first amount water is about 1.0:7.8:31.8 to about 1.0:11.6:47.6. In some
embodiments, the molar ratio present in the first mixture between (1aS,5aS)(4-oxy-pyrazin
yl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S)
hydroxymethyl-2,2-dimethyl-propyl)-amide, acetonitrile, and first amount water is about
1.0:8.2:33.7 to about 1.0:11.2:45.7. In some embodiments, the molar ratio present in the first
mixture between (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-
cyclopropa[a]pentalenecarboxylic acid ((S)hydroxymethyl-2,2-dimethyl-propyl)-amide,
acetonitrile, and first amount water is about 1.0:8.7:35.7 to about 1.0:10.7:43.7. In some
embodiments, the molar ratio present in the first mixture between (1aS,5aS)(4-oxy-pyrazin
yl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S)
hydroxymethyl-2,2-dimethyl-propyl)-amide, acetonitrile, and first amount water is about
1.0:9.2:37.0 to about 1.0:10.2:41.7. In some embodiments, the molar ratio present in the first
mixture between (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-
cyclopropa[a]pentalenecarboxylic acid ((S)hydroxymethyl-2,2-dimethyl-propyl)-amide,
acetonitrile, and first amount water is about 1.0:9.7:39.7. In some embodiments, adding of the
second amount of water to the first mixture is conducted at a rate that the temperature of the
mixture of the second amount of water together with the first mixture is at about 25 °C to about
80 °C. In some embodiments, adding of the second amount of water to the first mixture is
conducted at a rate that the temperature of the mixture of the second amount of water together
with the first mixture is at about 40 °C to about 70 °C. In some embodiments, adding of the
second amount of water to the first mixture is conducted at a rate that the temperature of the
mixture of the second amount of water together with the first mixture is at about 55 °C to about
65 °C. In some embodiments, adding of the second amount of water to the first mixture is
conducted at a rate that the temperature of the mixture of the second amount of water together
with the first mixture is at about 58 °C to about 62 °C. In some embodiments, adding of the
second amount of water to the first mixture is conducted at a rate that the temperature of the
mixture of the second amount of water together with the first mixture is at about 60 °C.
In some embodiments, the molar ratio present in the crystallizing mixture between
(1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalene
carboxylic acid ((S)hydroxymethyl-2,2-dimethyl-propyl)-amide, acetonitrile, and water is
about 1.0:7.3:327.4 to about 1.0:12.1:545.6. In some embodiments, the molar ratio present in the
crystallizing mixture between (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-
diaza-cyclopropa[a]pentalenecarboxylic acid ((S)hydroxymethyl-2,2-dimethyl-propyl)-
amide, acetonitrile, and water in the crystallizing mixture is about 1.0:7.8:349.2 to about
1.0:11.6:523.8. In some embodiments, the molar ratio present in the crystallizing mixture
between (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-
cyclopropa[a]pentalenecarboxylic acid ((S)hydroxymethyl-2,2-dimethyl-propyl)-amide,
acetonitrile, and water in the crystallizing mixture is about 1.0:8.2:371.0 to about 1.0:11.2:502.0.
In some embodiments, the molar ratio present in the crystallizing mixture between (1aS,5aS)
(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic
acid ((S)hydroxymethyl-2,2-dimethyl-propyl)-amide, acetonitrile, and water in the
crystallizing mixture is about 1.0:8.7:392.8 to about 1.0:10.7:480.1. In some embodiments, the
molar ratio present in the crystallizing mixture between (1aS,5aS)(4-oxy-pyrazinyl)-
1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S)
hydroxymethyl-2,2-dimethyl-propyl)-amide, acetonitrile, and water in the crystallizing mixture
is about 1.0:9.2:414.7 to about 1.0:10.2:458.3. In some embodiments, the molar ratio present in
the crystallizing mixture between (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-
diaza-cyclopropa[a]pentalenecarboxylic acid ((S)hydroxymethyl-2,2-dimethyl-propyl)-
amide, acetonitrile, and water in the crystallizing mixture is about 1.0:9.7:436.5.
In some embodiments, (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-
diaza-cyclopropa[a]pentalenecarboxylic acid ((S)hydroxymethyl-2,2-dimethyl-propyl)-
amide in the crystallizing and dissolving steps is selected from the group consisting of:
1) a dichloromethane solvate of (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-
tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S)hydroxymethyl-2,2-
dimethyl-propyl)-amide;
2) an acetone solvate of (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-
1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S)hydroxymethyl-2,2-dimethyl-
propyl)-amide;
3) a non-selective solvate of (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-
tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S)hydroxymethyl-2,2-
dimethyl-propyl)-amide; and
4) an ethyl acetate solvate of (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-
tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S)hydroxymethyl-2,2-
dimethyl-propyl)-amide; and
mixtures thereof.
In some embodiments, (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-
diaza-cyclopropa[a]pentalenecarboxylic acid ((S)hydroxymethyl-2,2-dimethyl-propyl)-
amide prior to the dissolving step is selected from the group consisting of:
1) a dichloromethane solvate of (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-
tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S)hydroxymethyl-2,2-
dimethyl-propyl)-amide;
2) an acetone solvate of (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-
1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S)hydroxymethyl-2,2-dimethyl-
propyl)-amide;
3) a non-selective solvate of (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-
tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S)hydroxymethyl-2,2-
dimethyl-propyl)-amide; and
4) an ethyl acetate solvate of (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-
tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S)hydroxymethyl-2,2-
dimethyl-propyl)-amide; and
mixtures thereof.
In some embodiments, isolating comprises filtering the crystalline form of (1aS,5aS)
(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic
acid ((S)hydroxymethyl-2,2-dimethyl-propyl)-amide from the crystallizing mixture.
In some embodiments, isolating comprises removing the crystalline form of (1aS,5aS)-
2-(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic
acid ((S)hydroxymethyl-2,2-dimethyl-propyl)-amide from the crystallizing mixture.
One aspect of the present invention relates to processes for preparing an anhydrous
crystalline form, the processes further comprise the step of drying the crystalline form of
(1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalene
carboxylic acid ((S)hydroxymethyl-2,2-dimethyl-propyl)-amide to obtain the anhydrous
crystalline form of (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-
cyclopropa[a]pentalenecarboxylic acid ((S)hydroxymethyl-2,2-dimethyl-propyl)-amide. In
some embodiments, drying is conducted at a temperature of about 15 °C to about 80 °C. In some
embodiments, drying is conducted at a temperature of about 25 °C to about 65 °C. In some
embodiments, drying is conducted at a temperature of about 35 °C to about 55 °C. In some
embodiments, drying is conducted at a temperature of about 50 °C. In some embodiments,
drying is conducted at a pressure of less than 760 mm Hg and a temperature of about 35 °C to
about 55 °C. In some embodiments, drying is conducted at a pressure of less than 760 mm Hg
and a temperature of about 55 °C to about 65 °C.
In some embodiments, after isolating, the anhydrous crystalline form of (1aS,5aS)(4-
oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid
((S)hydroxymethyl-2,2-dimethyl-propyl)-amide has a chemical purity of about 95% or
greater. In some embodiments, after isolating, the anhydrous crystalline form of (1aS,5aS)(4-
oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid
((S)hydroxymethyl-2,2-dimethyl-propyl)-amide has a chemical purity of about 98% or
greater. In some embodiments, after isolating, the anhydrous crystalline form of (1aS,5aS)(4-
oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid
((S)hydroxymethyl-2,2-dimethyl-propyl)-amide has a chemical purity of about 99% or
greater. In some embodiments, after isolating, the anhydrous crystalline form of (1aS,5aS)(4-
oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid
((S)hydroxymethyl-2,2-dimethyl-propyl)-amide has an enantiomeric excess of about 95% or
greater. In some embodiments, after isolating, the anhydrous crystalline form of (1aS,5aS)(4-
oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid
((S)hydroxymethyl-2,2-dimethyl-propyl)-amide has an enantiomeric excess of about 98% or
greater. In some embodiments, after isolating, the anhydrous crystalline form of (1aS,5aS)(4-
oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid
((S)hydroxymethyl-2,2-dimethyl-propyl)-amide has an enantiomeric excess of about 99% or
greater. In some embodiments, after isolating, the anhydrous crystalline form of (1aS,5aS)(4-
oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid
((S)hydroxymethyl-2,2-dimethyl-propyl)-amide has a chemical purity of about 99% or
greater and an enantiomeric excess of about 99% or greater.
One aspect of the present invention relates to an anhydrous crystalline form of
(1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalene
carboxylic acid ((S)hydroxymethyl-2,2-dimethyl-propyl)-amide prepared by a process
described herein.
One aspect of the present invention relates to processes of making a composition
comprising mixing an anhydrous crystalline form of (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-
tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S)hydroxymethyl-2,2-
dimethyl-propyl)-amide as described herein with a phamaceutically acceptable carrier.
One aspect of the present invention relates to processes of making a composition further
comprising forming the composition into drug product, such as, a tablet, a pill, a powder, a
lozenge, a sachet, a cachet, an elixir, a suspension, an emulsion, a solution, a syrup, a soft
gelatin capsule, a hard gelatin capsule, a suppository, a sterile injectable solution, or a sterile
packaged powder.
Crystalline Forms of Compound 1
One aspect of the present invention relates to anhydrous and solvate forms of (1aS,5aS)-
2-(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic
acid ((S)hydroxymethyl-2,2-dimethyl-propyl)-amide (Compound 1).
One aspect of the present invention relates to DCM solvates of (1aS,5aS)(4-oxy-
pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S)-
1-hydroxymethyl-2,2-dimethyl-propyl)-amide (Compound 1).
One aspect of the present invention relates to an anhydrous form of (1aS,5aS)(4-oxy-
pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S)-
1-hydroxymethyl-2,2-dimethyl-propyl)-amide (Compound 1).
One aspect of the present invention relates to acetone solvates of (1aS,5aS)(4-oxy-
pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S)-
1-hydroxymethyl-2,2-dimethyl-propyl)-amide (Compound 1).
One aspect of the present invention relates to non-selective solvates of (1aS,5aS)(4-
oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid
((S)hydroxymethyl-2,2-dimethyl-propyl)-amide (Compound 1).
One aspect of the present invention relates to ethyl acetate solvates of (1aS,5aS)(4-
oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid
((S)hydroxymethyl-2,2-dimethyl-propyl)-amide (Compound 1).
Crystalline forms of the solvates and anhydrous forms described herein can be identified
by their unique solid state signature with respect to, for example, differential scanning
calorimetry (DSC), powder X-ray diffraction (PXRD), and other solid state methods.
Further characterization with respect to water or solvent content of crystalline forms can
be gauged by any of the following methods for example, thermogravimetric analysis (TGA),
DSC and the like.
For DSC, it is known that the temperatures observed will depend upon sample purity,
the rate of temperature change, as well as sample preparation technique and the particular
instrument employed. Thus, the values reported herein relating to DSC thermograms can vary
by plus or minus about 4 °C (i.e., ± 4 °C). The values reported herein relating to DSC
thermograms can also vary by plus or minus about 20 joules per gram (i.e., ± 20 joules/gram).
In some embodiments, the DSC thermogram values reported herein relate to desolvation
events. When DSC thermogram values reported herein relate to desolvation events, the values
reported herein are estimates. Scan rate and pan closure can influence DSC values for
desolvation events, which can vary by plus or minus about 25 °C (i.e., ± 25 °C). DSC values for
desolvation events reported herein were recorded using a sample in an aluminum pan with an
uncrimped lid and a scan rate of 10 °C/min.
For PXRD, the relative intensities of the peaks can vary, depending upon the sample
preparation technique, the sample mounting procedure and the particular instrument employed.
Moreover, instrument variation and other factors can often affect the 2 values. Therefore, the
peak assignments of diffraction patterns can vary by plus or minus 0.2 °2 (i.e., ± 0.2 °2).
For TGA, the features reported herein can vary by plus or minus about 5 °C (i.e., ± 5
°C). The TGA features reported herein can also vary by plus or minus about 2% (i.e., ± 2%)
weight change due to, for example, sample variation.
Further characterization with respect to hygroscopicity of the crystalline forms can be
gauged by, for example, dynamic moisture sorption (DMS). The DMS features reported herein
can vary by plus or minus about 5% (i.e., ± 5%) relative humidity. The DMS features reported
herein can also vary by plus or minus about 5% (i.e., ± 5%) weight change.
1. Dichloromethane (DCM) solvates of Compound 1.
A. Compound 1 (DCM solvates)
One aspect of the present invention relates to DCM solvates of (1aS,5aS)(4-oxy-
pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S)-
1-hydroxymethyl-2,2-dimethyl-propyl)-amide (Compound 1). The DCM solvates of Compound
1 are characterized by PXRD. The physical properties for the DCM solvates as determined by
PXRD are summarized in Table 1 below.
Table 1
Compound 1 (DCM solvates)
Figure 2: Peaks of about 9.7 % relative intensity at 8.3, 9.6, 10.7,
PXRD
11.0, 15.0, 16.5, 16.7, 17.3, and 25.1 °2
The amount of DCM present in these solvates can vary, and be up to about 10.6% by
weight. The amount of DCM can readily be determined by TGA. The physical properties for a
DCM solvate from Example 1, Method 1, Step F are summarized in Table 2 below.
Table 2
Compound 1 (DCM solvates, Example 1, Method 1, Step F)
TGA Figure 1: Decrease in weight of about 5.9% out to about 150 °C
DSC Figure 1: Endotherm extrapolated onset temperature: about 163 °C
Certain powder X-ray diffraction peaks for the DCM solvates of (1aS,5aS)(4-oxy-
pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S)-
1-hydroxymethyl-2,2-dimethyl-propyl)-amide (Compound 1) are shown in Table 3 below.
Table 3
d-spacing Rel. Int. d-spacing Rel. Int.
Pos. [°2 .] Pos. [°2.]
[Å] [%] [Å] [%]
6.4 13.8 6.1 16.7 5.3 30.2
8.3 10.6 100.0 17.3 5.1 16.5
9.6 9.2 11.3 18.2 4.9 2.6
.7 8.3 15.6 18.7 4.7 5.6
11.0 8.0 24.3 19.5 4.6 2.3
11.8 7.5 2.2 20.4 4.4 6.1
12.5 7.1 2.7 21.6 4.1 7.7
13.8 6.4 4.5 24.1 3.7 5.3
14.4 6.1 7.3 25.1 3.5 46.0
.0 5.9 9.7 26.1 3.4 6.3
.8 5.6 6.0 28.6 3.1 4.3
16.5 5.4 13.9 29.1 3.1 2.6
B. Dichloromethane Hemi-solvate of Compound 1
One aspect of the present invention relates to the DCM hemi-solvate of (1aS,5aS)(4-
oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid
((S)hydroxymethyl-2,2-dimethyl-propyl)-amide (Compound 1). The DCM hemi-solvate of
Compound 1 was prepared by slow crystallization from CH Cl and hexanes (Example 2). The
crystal structure was solved and is shown in Figure 3.
2. Compound 1 (Anhydrous Form).
One aspect of the present invention relates to an anhydrous form of (1aS,5aS)(4-oxy-
pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S)-
1-hydroxymethyl-2,2-dimethyl-propyl)-amide (Compound 1). The physical properties of the
crystalline form of Compound 1 (anhydrous form) are summarized in Table 4 below.
Table 4
Compound 1 (Anhydrous Form)
Figure 6: Peaks of about 8.7% relative intensity at 8.5, 9.8, 10.7,
PXRD
11.1, 11.8, 14.5, 16.5, 16.9, 17.4, 18.9, 22.1, and 25.4 °2
TGA Figure 7: Decrease in weight of about 0.24% out to about 150 °C
DSC Figure 7: Endotherm extrapolated onset temperature: about 162 °C
Figure 7A: The adsorption/desorption isotherm shows about 1.0% or
less weight change from about 10% relative humidity (RH) to about
90% RH; and about 0.1% or less weight change after a 10% RH to
90% RH back to 10% RH cycle, See Example 13.
Certain powder X-ray diffraction peaks for the anhydrous form of (1aS,5aS)(4-oxy-
pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S)-
1-hydroxymethyl-2,2-dimethyl-propyl)-amide (Compound 1) are shown in Table 5 below.
Table 5
d-spacing d-spacing
Rel. Int. [%] Rel. Int. [%]
Pos. [°2.] Pos. [°2.]
[Å] [Å]
6.6 13.4 4.4 17.3 5.1 8.5
7.9 11.3 5.5 17.4 5.1 14.8
8.5 10.5 100.0 18.4 4.8 4.6
9.8 9.0 21.5 18.9 4.7 8.7
.7 8.3 28.3 20.2 4.4 5.5
11.1 7.9 26.1 20.9 4.3 4.4
11.8 7.5 10.0 22.1 4.0 14.5
13.8 6.4 7.5 23.4 3.8 3.0
14.5 6.1 11.3 24.7 3.6 4.6
14.9 6.0 6.0 25.4 3.5 26.6
16.0 5.6 5.8 26.5 3.4 8.1
16.5 5.4 11.8 29.2 3.1 2.8
16.9 5.2 26.7 29.3 3.0 3.6
One aspect of the present invention relates to an anhydrous crystalline form of
(1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalene
carboxylic acid ((S)hydroxymethyl-2,2-dimethyl-propyl)-amide.
One aspect of the present invention relates to an anhydrous crystalline form of
(1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalene
carboxylic acid ((S)hydroxymethyl-2,2-dimethyl-propyl)-amide, wherein the anhydrous
crystalline form has a powder X-ray diffraction pattern comprising a peak, in terms of 2 , at
8.5° ± 0.2°. In some embodiments, the anhydrous crystalline form has a powder X-ray
diffraction pattern comprising peaks, in terms of 2 , at 8.5° ± 0.2°, and 10.7° ± 0.2°. In some
embodiments, the anhydrous crystalline form has a powder X-ray diffraction pattern comprising
peaks, in terms of 2 , at 8.5° ± 0.2°, 10.7° ± 0.2°, and 16.9° ± 0.2°. In some embodiments, the
anhydrous crystalline form has a powder X-ray diffraction pattern comprising peaks, in terms of
2, at 8.5° ± 0.2°, 10.7° ± 0.2°, 16.9° ± 0.2°, 25.4° ± 0.2°, and 11.1° ± 0.2°. In some
embodiments, the anhydrous crystalline form has a powder X-ray diffraction pattern comprising
peaks, in terms of 2 , at 8.5° ± 0.2°, 10.7° ± 0.2°, 16.9° ± 0.2°, 25.4° ± 0.2°, 11.1° ± 0.2°, 9.8° ±
0.2°, and 17.4° ± 0.2°. In some embodiments, the anhydrous crystalline form has a powder X-
ray diffraction pattern comprising peaks, in terms of 2 , at 8.5° ± 0.2°, 10.7° ± 0.2°, 16.9° ±
0.2°, 25.4° ± 0.2°, 11.1° ± 0.2°, 9.8° ± 0.2°, 17.4° ± 0.2°, 22.1° ± 0.2°, and 16.5° ± 0.2°. In some
embodiments, the anhydrous crystalline form has a powder X-ray diffraction pattern comprising
peaks, in terms of 2 , at 8.5° ± 0.2°, 10.7° ± 0.2°, 16.9° ± 0.2°, 25.4° ± 0.2°, 11.1° ± 0.2°, 9.8° ±
0.2°, 17.4° ± 0.2°, 22.1° ± 0.2°, 16.5° ± 0.2°, 14.5° ± 0.2°, 11.8° ± 0.2°, and 18.9° ± 0.2°. In
some embodiments, the anhydrous crystalline form has a powder X-ray diffraction pattern
substantially as shown in Figure 6, wherein by “substantially” is meant that the reported peaks
can vary by about ± 0.2 °2 .
In some embodiments, the anhydrous crystalline form has a differential scanning
calorimetry thermogram comprising an endotherm with an extrapolated onset temperature
between about 159.6 °C and about 169.6 °C. In some embodiments, the anhydrous crystalline
form has a differential scanning calorimetry thermogram comprising an endotherm with an
extrapolated onset temperature between about 160.6 °C and about 168.6 °C. In some
embodiments, the anhydrous crystalline form has a differential scanning calorimetry
thermogram comprising an endotherm with an extrapolated onset temperature between about
162.6 °C and about 166.6 °C. In some embodiments, the anhydrous crystalline form has having
a differential scanning calorimetry thermogram comprising an endotherm with an extrapolated
onset temperature between about 163.6 °C and about 165.6 °C. In some embodiments, the
anhydrous crystalline form has a differential scanning calorimetry thermogram comprising an
endotherm with an extrapolated onset temperature at about 164.6 °C. In some embodiments, the
anhydrous crystalline form has a differential scanning calorimetry thermogram substantially as
shown in Figure 7, wherein by “substantially” is meant that the reported DSC features can vary
by about ± 4 °C and that the reported DSC features can vary by about ± 20 joules per gram.
In some embodiments, the anhydrous crystalline form has a thermogravimetric analysis
profile showing about 0.5% weight loss below about 135 °C. In some embodiments, the
anhydrous crystalline form has a thermogravimetric analysis profile showing about 0.25%
weight loss below about 135 °C. In some embodiments, the anhydrous crystalline form has a
thermogravimetric analysis profile showing about 0.05% weight loss below about 135 °C. In
some embodiments, the anhydrous crystalline form has a thermogravimetric analysis profile
substantially as shown in Figure 7, wherein by “substantially” is meant that the reported TGA
features can vary by about ± 5 °C, and that that the reported TGA features can vary by about ±
2% weight change.
One aspect of the present invention relates to the anhydrous crystalline form having:
1) a powder X-ray diffraction pattern comprising peaks, in terms of 2 , at 8.5° ±
0.2°, and 10.7° ± 0.2°;
2) a differential scanning calorimetry thermogram comprising an endotherm with
an extrapolated onset temperature between about 159.6 °C and about 169.6 °C; and/or
3) a thermogravimetric analysis profile showing about 0.5% weight loss below
about 135 °C.
One aspect of the present invention relates to the anhydrous crystalline form having:
1) a powder X-ray diffraction pattern comprising peaks, in terms of 2 , at 8.5° ±
0.2°, 10.7° ± 0.2°, and 16.9° ± 0.2°;
2) a differential scanning calorimetry thermogram comprising an endotherm with
an extrapolated onset temperature between about 160.6 °C and about 168.6 °C; and/or
3) a thermogravimetric analysis profile showing about 0.25% weight loss below
about 135 °C.
One aspect of the present invention relates to the anhydrous crystalline form having:
1) a powder X-ray diffraction pattern comprising peaks, in terms of 2 , at 8.5° ±
0.2°, 10.7° ± 0.2°, 16.9° ± 0.2°, 25.4° ± 0.2°, and 11.1° ± 0.2°;
2) a differential scanning calorimetry thermogram comprising an endotherm with
an extrapolated onset temperature between about 162.6 °C and about 166.6 °C; and/or
3) a thermogravimetric analysis profile showing about 0.05% weight loss below
about 135 °C.
One aspect of the present invention relates to the anhydrous crystalline form having:
1) a powder X-ray diffraction pattern comprising peaks, in terms of 2 , at 8.5° ±
0.2°, 10.7° ± 0.2°, 16.9° ± 0.2°, 25.4° ± 0.2°, 11.1° ± 0.2°, 9.8° ± 0.2°, and 17.4° ± 0.2°;
2) a differential scanning calorimetry thermogram comprising an endotherm with
an extrapolated onset temperature between about 163.6 °C and about 165.6 °C; and/or
3) a thermogravimetric analysis profile showing about 0.05% weight loss below
about 135 °C.
One aspect of the present invention relates to the anhydrous crystalline form having:
1) a powder X-ray diffraction pattern comprising peaks, in terms of 2 , at 8.5° ±
0.2°, 10.7° ± 0.2°, 16.9° ± 0.2°, 25.4° ± 0.2°, 11.1° ± 0.2°, 9.8° ± 0.2°, 17.4° ± 0.2°, 22.1° ±
0.2°, and 16.5° ± 0.2°;
2) a differential scanning calorimetry thermogram comprising an endotherm with
an extrapolated onset temperature at about 164.6 °C; and/or
3) a thermogravimetric analysis profile showing about 0.05% weight loss below
about 135 °C.
One aspect of the present invention relates to the anhydrous crystalline form having:
1) a powder X-ray diffraction pattern comprising peaks, in terms of 2 , at 8.5° ±
0.2°, 10.7° ± 0.2°, 16.9° ± 0.2°, 25.4° ± 0.2°, 11.1° ± 0.2°, 9.8° ± 0.2°, 17.4° ± 0.2°, 22.1° ±
0.2°, 16.5° ± 0.2°, 14.5° ± 0.2°, 11.8° ± 0.2°, and 18.9° ± 0.2°;
2) a differential scanning calorimetry thermogram comprising an endotherm with
an extrapolated onset temperature at about 164.6 °C; and/or
3) a thermogravimetric analysis profile showing about 0.05% weight loss below
about 135 °C.
One aspect of the present invention relates to the anhydrous crystalline form having:
1) a powder X-ray diffraction pattern substantially as shown in Figure 6;
2) a differential scanning calorimetry thermogram substantially as shown in
Figure 7; and/or
3) a thermogravimetric analysis profile substantially as shown in Figure 7.
3. Compound 1 (Acetone Solvates).
One aspect of the present invention relates to acetone solvates of (1aS,5aS)(4-oxy-
pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S)-
1-hydroxymethyl-2,2-dimethyl-propyl)-amide (Compound 1). The acetone solvates of
Compound 1 are characterized by PXRD. The physical properties for the acetone solvates as
determined by PXRD are summarized in Table 6 below.
Table 6
Compound 1 (Acetone Solvate)
Figure 8: Peaks of about 5.4% relative intensity at 7.1, 8.3,
PXRD
.1, 11.0, 13.7, 16.1, 16.6, 17.3, 22.7, 25.0, 25.6, and 26.0 °2
The amount of acetone present in these solvates can vary and can readily be determined
by TGA. The physical properties for a acetone solvate from Example 5 are summarized in
Table 7 below.
Table 7
Compound 1 (Acetone Solvate, Example 5)
TGA Figure 9: Decrease in weight of about 5.5% out to about 150 °C
DSC Figure 9: Endotherm extrapolated onset temperature: about 163 °C
Certain powder X-ray diffraction peaks for the acetone solvates of (1aS,5aS)(4-oxy-
pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S)-
1-hydroxymethyl-2,2-dimethyl-propyl)-amide (Compound 1) are shown in Table 8 below.
Table 8
d-spacing Rel. Int. d-spacing Rel. Int.
Pos. [°2 .] [Å] [%] Pos. [°2.] [Å] [%]
8.3 10.6266 100.0 6.1 14.41073 3.8
.0 3.56844 45.0 18.1 4.90385 3.5
16.6 5.34216 26.2 19.7 4.51452 3.5
17.3 5.1231 23.5 15.5 5.72733 3.3
11.0 8.04494 14.4 14.4 6.13613 3.2
.1 8.74974 9.2 24.7 3.61152 3.1
26.0 3.4277 8.8 20.8 4.26245 2.9
7.1 12.45547 8.3 9.5 9.35087 2.8
22.7 3.91113 7.7 29.8 3.00222 2.8
13.7 6.46525 6.9 19.5 4.54403 2.8
16.1 5.51282 6.3 19.9 4.4696 2.6
.6 3.47777 5.4 16.9 5.24284 2.6
18.8 4.72926 4.5 11.5 7.71311 2.5
.6 5.67632 4.4 19.1 4.65159 2.4
21.5 4.12408 3.9 27.7 3.22211 2.3
One aspect of the present invention relates to an acetone solvate of (1aS,5aS)(4-oxy-
pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S)-
1-hydroxymethyl-2,2-dimethyl-propyl)-amide.
One aspect of the present invention relates to an acetone solvate having a powder X-ray
diffraction pattern comprising a peak, in terms of 2 , at 8.3° ± 0.2°. In some embodiments, the
acetone solvate has a powder X-ray diffraction pattern comprising peaks, in terms of 2 , at 8.3°
± 0.2° and 25.0° ± 0.2°. In some embodiments, the acetone solvate has a powder X-ray
diffraction pattern comprising peaks, in terms of 2 , at 8.3° ± 0.2°, 25.0° ± 0.2°, and 16.6° ±
0.2°. In some embodiments, the acetone solvate has a powder X-ray diffraction pattern
comprising peaks, in terms of 2 , at 8.3° ± 0.2°, 25.0° ± 0.2°, 16.6° ± 0.2°, 17.3° ± 0.2°, and
11.0° ± 0.2°. In some embodiments, the acetone solvate has a powder X-ray diffraction pattern
comprising peaks, in terms of 2 , at 8.3° ± 0.2°, 25.0° ± 0.2°, 16.6° ± 0.2°, 17.3° ± 0.2°, 11.0° ±
0.2°, 10.1° ± 0.2°, and 26.0° ± 0.2°. In some embodiments, the acetone solvate has a powder X-
ray diffraction pattern comprising peaks, in terms of 2 , at 8.3° ± 0.2°, 25.0° ± 0.2°, 16.6° ±
0.2°, 17.3° ± 0.2°, 11.0° ± 0.2°, 10.1° ± 0.2°, 26.0° ± 0.2°, 7.1° ± 0.2°, and 22.7° ± 0.2°. In some
embodiments, the acetone solvate has a powder X-ray diffraction pattern comprising peaks, in
terms of 2 , at 8.3° ± 0.2°, 25.0° ± 0.2°, 16.6° ± 0.2°, 17.3° ± 0.2°, 11.0° ± 0.2°, 10.1° ± 0.2°,
26.0° ± 0.2°, 7.1° ± 0.2°, 22.7° ± 0.2°, 13.7° ± 0.2°, 16.1° ± 0.2°, and 25.6° ± 0.2°. In some
embodiments, the acetone solvate has a powder X-ray diffraction pattern substantially as shown
in Figure 8, wherein by “substantially” is meant that the reported peaks can vary by about ± 0.2
°2 .
In some embodiments, the acetone solvate has a differential scanning calorimetry
thermogram comprising an endotherm with an extrapolated onset temperature between about
158.0 °C and about 168.0 °C. In some embodiments, the acetone solvate has a differential
scanning calorimetry thermogram comprising an endotherm with an extrapolated onset
temperature between about 159.0 °C and about 167.0 °C. In some embodiments, the acetone
solvate has a differential scanning calorimetry thermogram comprising an endotherm with an
extrapolated onset temperature between about 161.0 °C and about 165.0 °C. In some
embodiments, the acetone solvate has a differential scanning calorimetry thermogram
comprising an endotherm with an extrapolated onset temperature between about 162.0 °C and
about 163.0 °C. In some embodiments, the acetone solvate has a differential scanning
calorimetry thermogram comprising an endotherm with an extrapolated onset temperature at
about 163.0 °C. In some embodiments, the acetone solvate has a differential scanning
calorimetry thermogram substantially as shown in Figure 9, wherein by “substantially” is meant
that the reported DSC features can vary by about ± 4 °C and that the reported DSC features can
vary by about ± 20 joules per gram.
In some embodiments, the acetone solvate has a thermogravimetric analysis profile
showing about 6.0% weight loss below about 150 °C. In some embodiments, the acetone solvate
has a thermogravimetric analysis profile showing about 5.75% weight loss below about 150 °C.
In some embodiments, the acetone solvate has a thermogravimetric analysis profile showing
about 5.5% weight loss or less below about 150 °C. In some embodiments, the acetone solvate
has a thermogravimetric analysis profile substantially as shown in Figure 9, wherein by
“substantially” is meant that the reported TGA features can vary by about ± 5 °C, and that that
the reported TGA features can vary by about ± 2% weight change.
One aspect of the present invention relates to the acetone solvate having:
1) a powder X-ray diffraction pattern comprising peaks, in terms of 2 , at 8.3° ±
0.2° and 25.0° ± 0.2°; and/or
2) a differential scanning calorimetry thermogram comprising an endotherm with
an extrapolated onset temperature between about 158.0 °C and about 168.0 °C.
One aspect of the present invention relates to the acetone solvate having:
1) a powder X-ray diffraction pattern comprising peaks, in terms of 2 , at 8.3° ±
0.2°, 25.0° ± 0.2°, and 16.6° ± 0.2°; and/or
2) a differential scanning calorimetry thermogram comprising an endotherm with
an extrapolated onset temperature between about 159.0 °C and about 167.0 °C.
One aspect of the present invention relates to the acetone solvate having:
1) a powder X-ray diffraction pattern comprising peaks, in terms of 2 , at 8.3° ±
0.2°, 25.0° ± 0.2°, 16.6° ± 0.2°, 17.3° ± 0.2°, and 11.0° ± 0.2°; and/or
2) a differential scanning calorimetry thermogram comprising an endotherm with
an extrapolated onset temperature between about 161.0 °C and about 165.0 °C.
One aspect of the present invention relates to the acetone solvate having:
1) a powder X-ray diffraction pattern comprising peaks, in terms of 2 , at 8.3° ±
0.2°, 25.0° ± 0.2°, 16.6° ± 0.2°, 17.3° ± 0.2°, 11.0° ± 0.2°, 10.1° ± 0.2°, and 26.0° ± 0.2°;
2) a differential scanning calorimetry thermogram comprising an endotherm with
an extrapolated onset temperature between about 162.0 °C and about 163.0 °C; and/or
3) a thermogravimetric analysis profile showing about 6.0% weight loss or less
below about 150 °C.
One aspect of the present invention relates to the acetone solvate having:
1) a powder X-ray diffraction pattern comprising peaks, in terms of 2, at 8.3° ±
0.2°, 25.0° ± 0.2°, 16.6° ± 0.2°, 17.3° ± 0.2°, 11.0° ± 0.2°, 10.1° ± 0.2°, 26.0° ± 0.2°, 7.1° ±
0.2°, and 22.7° ± 0.2°;
2) a differential scanning calorimetry thermogram comprising an endotherm with
an extrapolated onset temperature at about 163.0 °C; and/or
3) a thermogravimetric analysis profile showing about 5.75% weight loss below
about 150 °C.
One aspect of the present invention relates to the acetone solvate having:
1) a powder X-ray diffraction pattern comprising peaks, in terms of 2 , at 8.3° ±
0.2°, 25.0° ± 0.2°, 16.6° ± 0.2°, 17.3° ± 0.2°, 11.0° ± 0.2°, 10.1° ± 0.2°, 26.0° ± 0.2°, 7.1° ±
0.2°, 22.7° ± 0.2°, 13.7° ± 0.2°, 16.1° ± 0.2°, and 25.6° ± 0.2°;
2) a differential scanning calorimetry thermogram comprising an endotherm with
an extrapolated onset temperature at about 163.0 °C; and/or
3) a thermogravimetric analysis profile showing about 5.5% weight loss or less
below about 150 °C.
One aspect of the present invention relates to the acetone solvate having:
1) a powder X-ray diffraction pattern substantially as shown in Figure 8;
2) a differential scanning calorimetry thermogram substantially as shown in
Figure 9; and/or
3) a thermogravimetric analysis profile substantially as shown in Figure 9.
4. Compound 1 (Non-Selective Solvates).
One aspect of the present invention relates to non-selective solvates of (1aS,5aS)(4-
oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid
((S)hydroxymethyl-2,2-dimethyl-propyl)-amide (Compound 1). Non-selective solvates refer
to solvates that have substantially the same crystalline form as determined by PXRD, and
depending on the purity, after de-solvation will have similar extrapolated onset temperature (+/-
4.0 °C) as determined by DSC regardless what solvent or solvents were used to prepare the
solvate. It is understood that the TGA trace will vary from one non-selective solvate to another
and is primarily determined by the solvent used in the preparation, the solvate formed, and the
amount of the solvnet present in the solvate.
The non-selective solvates of Compound 1 are characterized by PXRD. The physical
properties for the non-selective solvates as determined by PXRD are summarized in Table 9
below.
Table 9
Compound 1 (Non-Selective Solvate)
Figure 10: Peaks of about 24 % relative intensity at 7.9, 9.9, 10.3, 10.7, 10.9,
PXRD
13.0, 14.9, 16.5, 17.4, 18.2, 18.3, 18.9, 19.9, 20.4, 20.5, 21.8, and 23.8 °2
The amount of the respective solvent present in these solvates can vary and can readily
be determined by TGA. One such non-selective solvate of Compound 1 is the ethyl acetate
solvate as described in Example 6 . The physical properties (i.e., TGA and DSC) for this ethyl
acetate non-selective solvate are summarized in Table 10 below.
Table 10
Compound 1 (Non-Selective Solvate/Ethyl Acetate, Example 6)
TGA Figure 13: Decrease in weight of about 4.8% out to about 150 °C
DSC Figure 13: Endotherm extrapolated onset temperature: about 161 °C
Certain powder X-ray diffraction peaks for the non-selective solvates of (1aS,5aS)(4-
oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid
((S)hydroxymethyl-2,2-dimethyl-propyl)-amide (Compound 1) are shown in Table 11 below.
Table 11
d-spacing d-spacing
Pos. [°2.] [Å] Rel. Int. [%] Pos. [°2.] [Å] Rel. Int. [%]
7.3 12.14275 16.7 19.2 4.62061 7.0
7.9 11.16727 39.7 19.6 4.53523 13.6
8.5 10.44535 11.7 19.9 4.47005 44.2
9.9 8.93424 37.9 20.4 4.35851 29.0
.3 8.61737 26.3 20.5 4.33052 32.8
.7 8.23598 26.3 21.2 4.1998 18.1
.9 8.12357 24.0 21.5 4.13161 14.7
11.3 7.81277 10.5 21.8 4.07567 37.1
13.0 6.82221 40.8 22.3 3.99444 8.1
13.3 6.64907 9.5 23.8 3.74137 43.5
14.9 5.92853 24.0 24.0 3.70405 16.7
.2 5.84616 11.2 24.4 3.64871 12.3
16.0 5.53769 21.1 24.7 3.60844 11.6
16.2 5.46327 11.9 24.9 3.57752 20.8
16.5 5.35726 24.5 25.1 3.54559 13.0
16.9 5.24138 10.7 25.5 3.49243 9.0
17.4 5.09682 36.7 26.0 3.43338 8.8
18.2 4.88174 100.0 27.7 3.22622 6.9
18.3 4.83505 44.3 27.9 3.19367 7.1
18.9 4.70738 24.3 28.3 3.14991 8.6
One aspect of the present invention relates to non-selective solvates of (1aS,5aS)(4-
oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid
((S)hydroxymethyl-2,2-dimethyl-propyl)-amide.
One aspect of the present invention relates to a non-selective solvate having a powder
X-ray diffraction pattern comprising a peak, in terms of 2 , at 18.2° ± 0.2°. In some
embodiments, the non-selective solvate has a powder X-ray diffraction pattern comprising
peaks, in terms of 2 , at 18.2° ± 0.2° and 18.3° ± 0.2°. In some embodiments, the non-selective
solvate has a powder X-ray diffraction pattern comprising peaks, in terms of 2 , at 18.2° ± 0.2°,
18.3° ± 0.2°, and 19.9° ± 0.2°. In some embodiments, the non-selective solvate has a powder X-
ray diffraction pattern comprising peaks, in terms of 2 , at 18.2° ± 0.2°, 18.3° ± 0.2°, 19.9° ±
0.2°, 23.8° ± 0.2°, and 13.0° ± 0.2°. In some embodiments, the non-selective solvate has a
powder X-ray diffraction pattern comprising peaks, in terms of 2 , at 18.2° ± 0.2°, 18.3° ± 0.2°,
19.9° ± 0.2°, 23.8° ± 0.2°, 13.0° ± 0.2°, 7.9° ± 0.2°, and 9.9° ± 0.2°. In some embodiments, the
non-selective solvate has a powder X-ray diffraction pattern comprising peaks, in terms of 2 , at
18.2° ± 0.2°, 18.3° ± 0.2°, 19.9° ± 0.2°, 23.8° ± 0.2°, 13.0° ± 0.2°, 7.9° ± 0.2°, 9.9° ± 0.2°, 21.8°
± 0.2°, and 17.4° ± 0.2°. In some embodiments, the non-selective solvate has a powder X-ray
diffraction pattern comprising peaks, in terms of 2 , at 18.2° ± 0.2°, 18.3° ± 0.2°, 19.9° ± 0.2°,
23.8° ± 0.2°, 13.0° ± 0.2°, 7.9° ± 0.2°, 9.9° ± 0.2°, 21.8° ± 0.2°, 17.4° ± 0.2°, 20.5° ± 0.2°, 20.4°
± 0.2°, 10.7° ± 0.2°, 10.3° ± 0.2°, 16.5° ± 0.2°, 18.9° ± 0.2°, 14.9° ± 0.2°, and 10.9° ± 0.2°. In
some embodiments, the non-selective solvate has a powder X-ray diffraction pattern
substantially as shown in Figure 10, wherein by “substantially” is meant that the reported peaks
can vary by about ± 0.2 °2 .
In some embodiments, the non-selective solvate has a differential scanning calorimetry
thermogram comprising an endotherm with an extrapolated onset temperature between about
159.8 °C and about 165.8 °C. In some embodiments, the non-selective solvate has a differential
scanning calorimetry thermogram comprising an endotherm with an extrapolated onset
temperature between about 160.8 °C and about 164.8 °C. In some embodiments, the non-
selective solvate has a differential scanning calorimetry thermogram comprising an endotherm
with an extrapolated onset temperature between about 158.8 °C and about 162.8 °C. In some
embodiments, the non-selective solvate has a differential scanning calorimetry thermogram
comprising an endotherm with an extrapolated onset temperature between about 159.8 °C and
about 161.8 °C. In some embodiments, the non-selective solvate has a differential scanning
calorimetry thermogram comprising an endotherm with an extrapolated onset temperature at
about 160.8 °C. In some embodiments, the non-selective solvate has a differential scanning
calorimetry thermogram substantially as shown in Figure 13, wherein by “substantially” is
meant that the reported DSC features can vary by about ± 4 °C and that the reported DSC
features can vary by about ± 20 joules per gram.
In some embodiments, the non-selective solvate has a thermogravimetric analysis
profile showing about 5.0% weight loss below about 150 °C. In some embodiments, the non-
selective solvate has a thermogravimetric analysis profile showing about 4.9% weight loss
below about 150 °C. In some embodiments, the non-selective solvate has a thermogravimetric
analysis profile showing about 4.8% weight loss below about 150 °C. In some embodiments, the
non-selective solvate has a thermogravimetric analysis profile substantially as shown in Figure
13, wherein by “substantially” is meant that the reported TGA features can vary by about ± 5
°C, and that that the reported TGA features can vary by about ± 2% weight change.
One aspect of the present invention relates to the non-selective solvate having:
1) a powder X-ray diffraction pattern comprising peaks, in terms of 2 , at 18.2° ±
0.2° and 18.3° ± 0.2°; and/or
2) a differential scanning calorimetry thermogram comprising an endotherm with
an extrapolated onset temperature between about 160.8 °C and about 165.8 °C.
One aspect of the present invention relates to the non-selective solvate having:
1) a powder X-ray diffraction pattern comprising peaks, in terms of 2 , at 18.2° ±
0.2°, 18.3° ± 0.2°, and 19.9° ± 0.2°; and/or
2) a differential scanning calorimetry thermogram comprising an endotherm with
an extrapolated onset temperature between about 160.8 °C and about 164.8 °C.
One aspect of the present invention relates to the non-selective solvate having:
1) a powder X-ray diffraction pattern comprising peaks, in terms of 2 , at 18.2° ±
0.2°, 18.3° ± 0.2°, 19.9° ± 0.2°, 23.8° ± 0.2°, and 13.0° ± 0.2°; and/or
2) a differential scanning calorimetry thermogram comprising an endotherm with
an extrapolated onset temperature between about 158.8 °C and about 162.8 °C.
One aspect of the present invention relates to the non-selective solvate having:
1) a powder X-ray diffraction pattern comprising peaks, in terms of 2 , at 18.2° ±
0.2°, 18.3° ± 0.2°, 19.9° ± 0.2°, 23.8° ± 0.2°, 13.0° ± 0.2°, 7.9° ± 0.2°, and 9.9° ± 0.2°;
2) a differential scanning calorimetry thermogram comprising an endotherm with
an extrapolated onset temperature between about 159.8 °C and about 161.8 °C; and/or
3) a thermogravimetric analysis profile showing about 5.0% weight loss below
about 150 °C.
One aspect of the present invention relates to the non-selective solvate having:
1) a powder X-ray diffraction pattern comprising peaks, in terms of 2 , at 18.2° ±
0.2°, 18.3° ± 0.2°, 19.9° ± 0.2°, 23.8° ± 0.2°, 13.0° ± 0.2°, 7.9° ± 0.2°, 9.9° ± 0.2°, 21.8° ± 0.2°,
and 17.4° ± 0.2°;
2) a differential scanning calorimetry thermogram comprising an endotherm with
an extrapolated onset temperature at about 160.8 °C; and/or
3) a thermogravimetric analysis profile showing about 4.9% weight loss below
about 150 °C.
One aspect of the present invention relates to the non-selective solvate having:
1) a powder X-ray diffraction pattern comprising peaks, in terms of 2 , at 18.2° ±
0.2°, 18.3° ± 0.2°, 19.9° ± 0.2°, 23.8° ± 0.2°, 13.0° ± 0.2°, 7.9° ± 0.2°, 9.9° ± 0.2°, 21.8° ± 0.2°,
17.4° ± 0.2°, 20.5° ± 0.2°, 20.4° ± 0.2°, 10.7° ± 0.2°, 10.3° ± 0.2°, 16.5° ± 0.2°, 18.9° ± 0.2°,
14.9° ± 0.2°, and 10.9° ± 0.2°;
2) a differential scanning calorimetry thermogram comprising an endotherm with
an extrapolated onset temperature at about 160.8 °C; and/or
3) a thermogravimetric analysis profile showing about 4.8% weight loss below
about 150 °C.
One aspect of the present invention relates to the non-selective solvate having:
1) a powder X-ray diffraction pattern substantially as shown in Figure 10;
2) a differential scanning calorimetry thermogram substantially as shown in
Figure 13; and/or
3) a thermogravimetric analysis profile substantially as shown in Figure 13.
. Compound 1 (Ethyl Acetate Solvate).
One aspect of the present invention relates to the ethyl acetate solvate of (1aS,5aS)(4-
oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid
((S)hydroxymethyl-2,2-dimethyl-propyl)-amide (Compound 1). The ethyl acetate solvate of
Compound 1 is characterized by PXRD. The physical properties for the ethyl acetate solvate as
determined by PXRD are summarized in Table 12 below.
Table 12
Compound 1 (Ethyl Acetate Solvate)
Figure 16: Peaks of about 16.0% relative intensity at 8.1, 8.3,
PXRD
9.0, 12.8, 14.2, 16.1, 16.7, 17.3, 17.9, 18.4, 22.9, 24.7, and 25.7 °2
The amount of ethyl acetate present in this solvate can vary but can readily be
determined by TGA. The physical properties for a the non-selective solvate as the ethyl acetate
solvate from Example 7 are summarized in Table 13 below.
Table 13
Compound 1 (Non-Selective Solvate/Ethyl Acetate, Example 7)
Figure 17: Decrease in weight of about 4.7% by weight out to about
120 °C
DSC Figure 17: Endotherm extrapolated onset temperature: about 121 °C
Certain powder X-ray diffraction peaks for the crystalline form of ethyl acetate solvates
of (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalene-
4-carboxylic acid ((S)hydroxymethyl-2,2-dimethyl-propyl)-amide (Compound 1) are shown
in Table 14 below.
Table 14
d-spacing Rel. Int. d-spacing Rel. Int.
Pos. [°2.] [Å] [%] Pos. [°2.] [Å] [%]
6.0 14.7 9.0 18.4 4.8 27.4
8.1 10.9 36.8 19.7 4.5 6.7
d-spacing Rel. Int. d-spacing Rel. Int.
Pos. [°2.] [Å] [%] Pos. [°2.] [Å] [%]
8.3 10.6 100.0 21.5 4.1 10.1
9.0 9.8 47.5 21.6 4.1 9.8
.1 8.8 11.6 21.8 4.1 5.7
11.4 7.8 6.4 22.9 3.9 18.6
12.8 6.9 37.1 23.4 3.8 10.7
14.2 6.3 39.8 23.7 3.8 10.6
14.6 6.1 7.4 24.7 3.6 22.4
.3 5.8 14.9 25.1 3.5 13.7
16.1 5.5 16.9 25.7 3.5 21.0
16.3 5.4 13.4 26.4 3.4 15.6
16.7 5.3 37.1 26.8 3.3 4.6
17.3 5.1 24.8 28.5 3.1 6.7
17.9 5.0 27.1 29.4 3.0 5.3
One aspect of the present invention relates to ethyl acetate solvates of (1aS,5aS)(4-
oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid
((S)hydroxymethyl-2,2-dimethyl-propyl)-amide.
One aspect of the present invention relates to an ethyl acetate solvate having a powder
X-ray diffraction pattern comprising a peak, in terms of 2 , at 8.3° ± 0.2°. In some
embodiments, the ethyl acetate solvate has a powder X-ray diffraction pattern comprising peaks,
in terms of 2 , at 8.3° ± 0.2° and 9.0° ± 0.2°. In some embodiments, the ethyl acetate solvate has
a powder X-ray diffraction pattern comprising peaks, in terms of 2 , at 8.3° ± 0.2°, 9.0° ± 0.2°,
and 14.2° ± 0.2°. In some embodiments, the ethyl acetate solvate has a powder X-ray diffraction
pattern comprising peaks, in terms of 2 , at 8.3° ± 0.2°, 9.0° ± 0.2°, 14.2° ± 0.2°, 16.7° ± 0.2°,
and 12.8° ± 0.2°. In some embodiments, the ethyl acetate solvate has a powder X-ray diffraction
pattern comprising peaks, in terms of 2 , at 8.3° ± 0.2°, 9.0° ± 0.2°, 14.2° ± 0.2°, 16.7° ± 0.2°,
12.8° ± 0.2°, 8.1° ± 0.2°, and 18.4° ± 0.2°. In some embodiments, the ethyl acetate solvate has a
powder X-ray diffraction pattern comprising peaks, in terms of 2 , at 8.3° ± 0.2°, 9.0° ± 0.2°,
14.2° ± 0.2°, 16.7° ± 0.2°, 12.8° ± 0.2°, 8.1° ± 0.2°, 18.4° ± 0.2°, 17.9° ± 0.2°, and 17.3° ± 0.2°.
In some embodiments, the ethyl acetate solvate has a powder X-ray diffraction pattern
comprising peaks, in terms of 2 , at 8.3° ± 0.2°, 9.0° ± 0.2°, 14.2° ± 0.2°, 16.7° ± 0.2°, 12.8° ±
0.2°, 8.1° ± 0.2°, 18.4° ± 0.2°, 17.9° ± 0.2°, 17.3° ± 0.2°, 24.7° ± 0.2°, 25.7° ± 0.2°, 22.9° ±
0.2°, and 16.1° ± 0.2°. In some embodiments, the ethyl acetate solvate has a powder X-ray
diffraction pattern substantially as shown in Figure 16, wherein by “substantially” is meant that
the reported peaks can vary by about ± 0.2 °2 .
In some embodiments, the ethyl acetate solvate has a differential scanning calorimetry
thermogram comprising an endotherm with an extrapolated onset temperature between about
116.4 °C and about 126.4 °C. In some embodiments, the ethyl acetate solvate has a differential
scanning calorimetry thermogram comprising an endotherm with an extrapolated onset
temperature between about 117.4 °C and about 125.4 °C. In some embodiments, the ethyl
acetate solvate has a differential scanning calorimetry thermogram comprising an endotherm
with an extrapolated onset temperature between about 119.4 °C and about 123.4 °C. In some
embodiments, the ethyl acetate solvate has a differential scanning calorimetry thermogram
comprising an endotherm with an extrapolated onset temperature between about 120.4 °C and
about 122.4 °C. In some embodiments, the ethyl acetate solvate has a differential scanning
calorimetry thermogram comprising an endotherm with an extrapolated onset temperature at
about 121.4 °C. In some embodiments, the ethyl acetate solvate has a differential scanning
calorimetry thermogram substantially as shown in Figure 17, wherein by “substantially” is
meant that the reported DSC features can vary by about ± 4 °C and that the reported DSC
features can vary by about ± 20 joules per gram.
In some embodiments, the ethyl acetate solvate has a thermogravimetric analysis profile
showing about 5.5% weight loss below about 135 °C. In some embodiments, the ethyl acetate
solvate has a thermogravimetric analysis profile showing about 5.4% weight loss below about
135 °C. In some embodiments, the ethyl acetate solvate has a thermogravimetric analysis profile
showing about 5.3% weight loss below about 135 °C. In some embodiments, the ethyl acetate
solvate has a thermogravimetric analysis profile substantially as shown in Figure 17, wherein
by “substantially” is meant that the reported TGA features can vary by about ± 5 °C, and that
that the reported TGA features can vary by about ± 2% weight change.
One aspect of the present invention relates to the ethyl acetate solvate having:
1) a powder X-ray diffraction pattern comprising peaks, in terms of 2 , at 8.3° ±
0.2° and 9.0° ± 0.2°; and/or
2) a differential scanning calorimetry thermogram comprising an endotherm with
an extrapolated onset temperature between about 116.4 °C and about 126.4 °C.
One aspect of the present invention relates to the ethyl acetate solvate having:
1) a powder X-ray diffraction pattern comprising peaks, in terms of 2 , at 8.3° ±
0.2°, 9.0° ± 0.2°, and 14.2° ± 0.2°; and/or
2) a differential scanning calorimetry thermogram comprising an endotherm with
an extrapolated onset temperature between about 117.4 °C and about 125.4 °C.
One aspect of the present invention relates to the ethyl acetate solvate having:
1) a powder X-ray diffraction pattern comprising peaks, in terms of 2 , at 8.3° ±
0.2°, 9.0° ± 0.2°, 14.2° ± 0.2°, 16.7° ± 0.2°, and 12.8° ± 0.2°; and/or
2) a differential scanning calorimetry thermogram comprising an endotherm with
an extrapolated onset temperature between about 119.4 °C and about 123.4 °C.
One aspect of the present invention relates to the ethyl acetate solvate having:
1) a powder X-ray diffraction pattern comprising peaks, in terms of 2 , at 8.3° ±
0.2°, 9.0° ± 0.2°, 14.2° ± 0.2°, 16.7° ± 0.2°, 12.8° ± 0.2°, 8.1° ± 0.2°, and 18.4° ± 0.2°;
2) a differential scanning calorimetry thermogram comprising an endotherm with
an extrapolated onset temperature between about 120.4 °C and about 122.4 °C; and/or
3) a thermogravimetric analysis profile showing about 5.5% weight loss below
about 135 °C.
One aspect of the present invention relates to the ethyl acetate solvate having:
1) a powder X-ray diffraction pattern comprising peaks, in terms of 2 , at 8.3° ±
0.2°, 9.0° ± 0.2°, 14.2° ± 0.2°, 16.7° ± 0.2°, 12.8° ± 0.2°, 8.1° ± 0.2°, 18.4° ± 0.2°, 17.9° ± 0.2°,
and 17.3° ± 0.2°;
2) a differential scanning calorimetry thermogram comprising an endotherm with
an extrapolated onset temperature at about 121.4 °C; and/or
3) a thermogravimetric analysis profile showing about 5.4% weight loss below
about 135 °C.
One aspect of the present invention relates to the ethyl acetate solvate having:
1) a powder X-ray diffraction pattern comprising peaks, in terms of 2 , at 8.3° ±
0.2°, 9.0° ± 0.2°, 14.2° ± 0.2°, 16.7° ± 0.2°, 12.8° ± 0.2°, 8.1° ± 0.2°, 18.4° ± 0.2°, 17.9° ± 0.2°,
17.3° ± 0.2°, 24.7° ± 0.2°, 25.7° ± 0.2°, 22.9° ± 0.2°, and 16.1° ± 0.2°;
2) a differential scanning calorimetry thermogram comprising an endotherm with
an extrapolated onset temperature at about 121.4 °C; and/or
3) a thermogravimetric analysis profile showing about 5.3% weight loss below
about 135 °C.
One aspect of the present invention relates to the ethyl acetate solvate having:
1) a powder X-ray diffraction pattern substantially as shown in Figure 16;
2) a differential scanning calorimetry thermogram substantially as shown in
Figure 17; and/or
3) a thermogravimetric analysis profile substantially as shown in Figure 17.
The crystalline forms described herein can be prepared by any of the suitable procedures
known in the art for preparing crystalline polymorphs. In some embodiments the crystalline
forms described herein are prepared according to the Examples. In some embodiments, the
crystalline forms described herein can be prepared by heating crystalline forms other than the
crystalline forms described herein. In some embodiments, the crystalline forms described herein
can be prepared by recrystallizing crystalline forms other than the crystalline forms described
herein.
Compound 1 of the present invention may be prepared according to relevant published
literature procedures that are used by one skilled in the art. Exemplary reagents and procedures
for these reactions appear hereinafter in the working Examples. Protection and deprotection may
be carried out by procedures generally known in the art (see, for example, Greene, T. W. and
Wuts, P. G. M., Protecting Groups in Organic Synthesis, 3 Edition, 1999 [Wiley]).
It is understood that the present invention embraces each enantiomer and mixtures
thereof. Separation of the individual isomers (such as, by chiral HPLC, recrystallization of
diastereoisomeric mixtures and the like) or selective synthesis (such as, by enantiomeric
selective syntheses and the like) of the individual isomers is accomplished by application of
various methods which are well known to practitioners in the art.
INDICATIONS AND METHODS OF PROPHYLAXIS AND/OR TREATMENT
In addition to the foregoing beneficial uses for the modulators of cannabinoid receptor
activity disclosed herein, the compounds disclosed herein are useful in the treatment of several
additional diseases and disorders, and in the amelioration of symptoms thereof. Without limitation,
these include the following:
1. PAIN.
The analgesic properties of cannabinoids have been recognized for many years. For
example, animal studies have demonstrated that the CB /CB agonists anandamide, THC,
CP55,940 and WIN 55212-2 are effective against acute and chronic pain from chemical,
mechanical, and thermal pain stimuli (reviewed in Walker and Huang (2002) Pharmacol. Ther.
95:127-135; reviewed in Pacher, P et al. (2006) Pharmacol. Rev. 58(3): 389-462). In humans,
topical administration of the CB /CB agonist HU-210 attenuates capsaicin-induced
hyperalgesia and allodynia (Rukwied, R. et al. (2003) Pain 102:283-288), and co-administration
of the CB /CB agonist THC and cannabidiol (nabiximols, trademark Sativex®) provides relief
from cancer-associated pain (GW Pharmaceuticals press release Jan 19, 2005, Jun 19, 2007) and
multiple-sclerosis-associated pain and spasticity (GW Pharmaceuticals press release Sept 27,
2005, Mar 11, 2009).
The role of CB in mediating these analgesic effects is well-documented (reviewed in
Manzanares, J. et al. (2006) Current Neuropharmacology 4:239-57; reviewed in Pacher, P. et al.
(2006) Pharmacol. Rev. 58(3): 389-462). For example, blockade of peripheral or central CB
leads to hyperalgesia (Richardson, J. D. et al. (1997) Eur. J. Pharmacol. 345:145-153;
Calignano, A. et al. (1998) Nature 394:277-281), whereas CB activation by exogenous
administration of a CB agonist arachidonylchloroethylamide reduces pain (Furuse, S. et al.
(2009) Anesthesiology 111(1):173-86).
Although less well-documented, CB also plays a role in mediating analgesic effects of
cannabinoids (reviewed in Guindon and Hohmann (2008) Br. J. Pharmacol. 153:319-334). For
example, systemic delivery of the CB -selective agonist AM1241 suppresses hyperalgesia
induced in the carrageenan, capsaicin, and formalin models of inflammatory pain in rodents
(reviewed in Guindon and Hohmann (2008) Br. J. Pharmacol. 153:319-334). Local
(subcutaneous) or systemic administration of AM1241 also reverses tactile and thermal
hypersensitivity in rats following ligation of spinal nerves in the chronic constriction injury
model of neuropathic pain (Malan, T. P. et al. (2001) Pain 93:239-245; Ibrahim, M. M. et al.
(2003) Proc. Natl. Acad. Sci. 100(18):10529-10533), an effect which is inhibited by treatment
with the CB -selective antagonist AM630 (Ibrahim, M. M. et al. (2005) Proc. Natl. Acad. Sci.
102(8):3093-8). The CB -selective agonist GW405833 administered systemically significantly
reverses hypersensitivity to mechanical stimuli in rats following ligation of spinal nerves (Hu, B.
et al. (2009) Pain 143:206-212). Thus, CB -selective agonists have also been demonstrated to
attenuate pain in experimental models of acute, inflammatory, and neuropathic pain, and
hyperalgesia.
Accordingly, CB -specific agonists and/or CB /CB agonists find use in the treatment
2 1 2
and/or prophylaxis of acute nociception and inflammatory hyperalgesia, as well as the allodynia
and hyperalgesia produced by neuropathic pain. For example, these agonists are useful as an
analgesic to treat pain arising from autoimmune conditions; allergic reactions; bone and joint
pain; muscle pain; dental pain; nephritic syndrome; scleroderma; thyroiditis; migraine and other
headache pain; pain associated with diabetic neuropathy; fibromyalgia, HIV-related neuropathy,
sciatica, and neuralgias; pain arising from cancer; and pain that occurs as an adverse affect of
therapeutics for the treatment of disease.
Furthermore, although cannabinoids exert their antinociceptive effects by complex
mechanisms involving effects on the central nervous system, spinal cord, and peripheral sensory
nerves (reviewed in Pacher, P. et al. (2006) Pharmacol. Rev. 58(3): 389-462), an analysis of
models of inflammatory and neuropathic pain in mice that are deficient for CB only in
nociceptive neurons localized in the peripheral nervous system demonstrates that the
contribution of CB -type receptors expressed on the peripheral terminals of nociceptors to
cannabinoid-induced analgesia is paramount (Agarwal, N. et al. (2007) Nat. Neurosci. 10(7):
870-879). Accordingly, CB agonists that are unable to cross the blood brain barrier still find use
in the treatment and/or prophylaxis of acute pain, inflammatory pain, neuropathic pain, and
hyperalgesia.
2. DISORDERS OF THE IMMUNE SYSTEM.
Autoimmune disorders. Cannabinoid receptor agonists have been demonstrated to
attenuate aberrant immune responses in autoimmune disorders, and in some cases, to provide
protection to the tissue that is being inappropriately targeted by the immune system.
For example, Multiple Sclerosis (MS) is an autoimmune disorder that results in the
demyelination of neurons in the CNS. The CB /CB agonist THC significantly inhibits the
severity of clinical disease in the Experimental Autoimmune Encephalomyelitis (EAE) mouse
model of MS, an effect that is believed to be mediated by CB on neurons and CB on immune
cell (Maresz, K. et al. (2007) Nat. Med. 13(4):492-497). Consistent with these results, CB -
selective agonist WIN 55212-2 provides significant neuroprotection in the experimental allergic
uveitis (EAU) model in mice (Pryce, G. et al. (2003) Brain 126:2191-2202), whereas CB -
selective agonist HU-308 markedly reduces the recruitment of immature myeloid cells and T
cells, microglial and infiltrating myeloid cell proliferation, and axonal loss in the EAE model
(Palazuelos, J. et al. (2008). J. Biol. Chem. 283(19):13320-9). Likewise, the CB /CB agonist
WIN 55212-2 significantly inhibits leukocyte rolling and adhesion in the brain in the EAE
mouse model, an effect that is blocked by the CB -selective antagonist SR144528 but not the
CB -selective antagonist SR141716A (Ni, X. et al. Mult. Sclerosis 10(2):158-64). Accordingly,
CB -selective agonists and/or CB /CB agonists find use in the treatment and/or prophylaxis of
2 1 2
Multiple Sclerosis and related autoimmune demyelinating diseases, e.g. Guillan-Barré
syndrome, polyradiculoneuropathy and chronic inflammatory demyelination.
As another example, the autoimmune disease Rheumatoid Arthritis (RA) is a chronic,
systemic inflammatory disorder of the skeletal system that principally attacks the joints to
produce an inflammatory synovitis and that often progresses to destruction of the articular
cartilage and ankylosis of the joints. The CB /CB agonists WIN 55212-2 and HU-210
significantly inhibit IL-1alpha-stimulated proteoglycan and collagen degradation in bovine nasal
cartilage explants in vitro (Mbvundula, E. et al. (2006) J. Pharm. and Pharmacol. 58:351-358).
Accordingly, CB -selective agonists and/or CB /CB agonists find use in the treatment and/or
2 1 2
prophylaxis of autoimmune arthritic diseases, for example, rheumatoid arthritis, psoriatic
arthritis, ankylosing spondylarthritis, and reactive arthritis.
Type 1 Hypersensitivity and Allergic response. Cannabinoid receptor agonists have
been demonstrated to attenuate aberrant immune responses in allergic reactions as well. In type-
1, or immediate, hypersensitivity, plasma cells that have been activated by an allergen secrete
IgE antibodies, which bind to Fc receptors on the surface of tissue mast cells and blood
basophils and eosinophils. Repeated exposure to the same allergen results in cross-linking of the
bound IgE on sensitized cells, resulting in secretion of pharmacologically active mediators such
as histamine, leukotriene and prostaglandin. These mediators are responsible for the symptoms
associated with allergies, including vasodilation and increased permeability, smooth muscle
spasms, and leukocyte extravasation. Topical administration of the CB /CB agonist HU-210
reduces these histamine-induced responses in human skin (Dvorak, M. et al. (2003) Inflamm.
Res. 52:238-245). Similarly, subcutaneous injection of CB /CB agonist THC or increased levels
of endogenous cannabinoids reduces cutaneous inflammation and the pruritis (itch) associated
with it in a mouse model for allergic contact dermatitis. (Karsak et al. (2007) Science,
316(5830), 1494-1497). In contrast, injection of the CB receptor antagonist S141716A or the
CB receptor antagonist SR144528 exacerbates this inflammation and pruritis. (Karsak et al.
(2007) Science, 316(5830), 1494-1497). Accordingly, CB -selective agonists and/or CB /CB
2 1 2
agonists find use in the treatment of allergic reactions including atopic dermatitis (pruritis/itch),
urticaria (hives), asthma, conjunctivitis, allergic rhinitis (hay fever), and anaphylaxis.
Conditions Associated with CNS Inflammation. CB agonists have been
demonstrated to attenuate inflammation in the CNS. For example, administration of CB
agonists prevents the activation of microglia in rodent models of Alzheimer’s Disease (Ashton J.
C., et al. (2007) Curr. Neuropharmacol. 5(2):73-80). Likewise, administration of CB agonists
reduces the volume of infarcts by 30% in a rodent occlusion model of stroke (Zhang, M. et al.
(2007) J. Cereb. Blood Flow Metab. 27:1387-96). Thus, CB agonists find use in the treatment
and/or prophylaxis of neuropathologies associated with CNS inflammation, e.g. Alzheimer's,
stroke-induced damage, dementia, ALS, and HIV.
Conditions Associated with Vascular Inflammation. CB is expressed in
macrophages and T cells in atherosclerotic plaques, and the CB /CB agonist THC reduces the
progression of atherosclerosis in ApoE knockout mice, a well studied mouse model of
atherosclerosis. The CB -specific antagonist SR144528 completely blocks this effect in vitro
and in vivo (Steffens, S. et al. (2005) Nature 434:782-786). Thus, CB agonists find use in
treating atherosclerosis.
Other Disorders Associated with Aberrant or Unwanted Immune Response. Given
the expression of CB on a number of different types of immune cells and the attenuating effects
that CB agonists have been observed to have on the activities of these cells, CB agonists are
useful for the treatment and/or prophylaxis of other disorders wherein undesired immune cell
activity and/or inflammation is observed. Such exemplary disorders include osteoarthritis,
anaphylaxis, Behcet’s disease, graft rejection, vasculitis, gout, spondylitis, viral and bacterial
diseases, e.g. AIDS, and meningitis; and other autoimmune disorders such as lupus, e.g.
systemic lupus erythematosus; inflammatory bowel disease, e.g. Crohn’s disease, ulcerative
colitis; psoriasis; autoimmune hepatitis; and type 1 diabetes mellitus.
3. BONE AND JOINT DISEASES.
Osteoporosis. CB is expressed in osteoblasts, osteocytes, and osteoclasts. Osteoblasts
make new bone, whereas osteoclasts degrade it. The CB -specific agonist HU-308 enhances
endocortical osteoblast numbers and activity while simultaneously inhibiting proliferation of
osteoclast precursors in bone marrow-derived osteoblasts/stromal cells in vitro, and attenuates
ovariectomy-induced bone loss and stimulates cortical thickness by stimulating endocortical
bone formation and suppressing osteoclast number in vivo (Ofek, O. et al. (2006) Proc. Natl.
Acad. Sci. 103(3):696-701). Thus, CB agonists are useful for the treatment and/or prophylaxis
of disease wherein bone density is decreased, such as osteoporosis.
Arthritis. As discussed above, CB -selective agonists and CB /CB agonists are useful
2 1 2
for the treatment and/or prophylaxis of autoimmune arthritic diseases, for example, rheumatoid
arthritis, psoriatic arthritis, ankylosing spondylarthritis, and reactive arthritis, and for the
treatment and/or prophylaxis of inflammation associated with osteoarthritis. In addition, as
discussed above, CB -selective agonists and CB /CB agonists are useful for the treatment of
1 1 2
pain associated with these arthritic disorders.
4. EYE DISEASE.
Retinal pigment epithelial (RPE) cells provide trophic support to photoreceptor cells in
the eye, and RPE cell death has been demonstrated to be a major contributor to Age-related
Macular Degeneration (AMD). The CB /CB agonist CP55940 significantly protects RPE cells
from oxidative damage; the CB receptor agonist, JWH015 provides comparable protection
(Wei, Y. et al. (2009) Mol. Vis. 15:1243-51). Accordingly, CB -selective agonists find use in
preventing the onset or progression of vision loss associated with AMD.
. COUGH.
The cough reflex is predominantly under the control of two classes of sensory afferent
nerve fibers, the myelinated A-delta fibers and the non-myelinated C-fibers, the activation of
which (i.e. depolarization) elicits cough via the vagus nerve afferent pathway. The CB /CB
agonist CP55940 reduces capsaicin-, PGE - and hypertonic saline-induced depolarization of
guinea pig and human vagus nerve preparations in vitro (Patel, H. J. et al. (2003) British J.
Pharma. 140:261-8). The CB /CB agonists WIN 55212-2 produced a dose-dependent inhibition
of the number of capsaicin-induced coughs in mice (Morita, K. et al. (2003) Eur. J. Pharmacol.
474:269-272). The CB /CB agonist anandamide produced a dose-dependent inhibition of the
number of capsaicin-induced coughs in guinea pigs (Calignano, A. et al. (2000) Nature 408:96-
101). CB -specific antagonist SR141716A attenuates the antitussive effects of WN 55212-2 and
anandamide (Morita, K. et al. (2003) Eur. J. Pharmacol. 474:269-272; Calignano, A. et al.
(2000) Nature 408:96-101). The CB -selective agonist JWH133 reduces capsaicin-, PGE - and
hypertonic saline-induced depolarization of guinea pig and human vagus nerve preparations in
vitro, and administration of CB -selective agonist JWH133 prior to exposure to the tussive agent
citric acid significantly reduces cough in conscious guinea-pigs (Patel, H. J. et al. (2003) British
J. Pharma. 140:261-8). Thus, both CB and CB play an important role in mediating the
antitussive effect of cannabinoids, and CB -selective agonists and CB /CB agonists are useful
1 1 2
in the treatment and/or prophylaxis of cough.
6. CANCER.
A number of human leukemia and lymphoma cell lines, including Jurkat, Molt-4 and
Sup-T1, express CB and not CB , and agonists of CB induce apoptosis in these and primary
2 1 2
acute lymphoblastic leukemia (ALL) cells (Nagarkatti, L. C. et al. US2004/0259936). Similarly,
CB is expressed on glioblastoma cell lines and treatment with agonists of CB induces
apoptosis of these cells in vitro (Widmer, M. (2008) J. Neurosci. Res. 86(14):3212-20).
Accordingly, CB -selective agonists are useful in attenuating the growth of a malignancy of the
immune system, for example, leukemias, lymphomas, and solid tumors of the glial lineage.
In addition, as discussed above, CB -selective agonists and CB /CB agonists are useful
1 1 2
in providing relief from pain associated with cancer (GW Pharmaceuticals press release Jan 19,
2005, Jun 19, 2007).
CB -mediated signaling is involved in the in vivo and in vitro growth inhibition of
prostate cancer cells, which suggests that CB agonists have potential therapeutic interest in the
management of prostate cancer. (Inhibition of human tumour prostate PC-3 cell growth by
cannabinoids R(+)-Methanandamide and JWH-015: Involvement of CB ; Olea-Herrero, et al.
British Journal of Cancer advance online publication 18 August 2009; doi: 10.1038/sj.bjc.
6605248).
7. REGENERATIVE MEDICINE.
Agonists of CB modulate the expansion of the progenitor pool of neurons in the CNS.
CB antagonists inhibit the proliferation of cultured neural stem cells and the proliferation of
progenitor cells in the SVZ of young animals, whereas CB -selective agonists stimulate
progenitor cell proliferation in vivo, with this effect being more pronounced in older animals
(Goncalves, M. B. et al. (2008) Mol. Cell Neurosci. 38(4):526-36). Thus, agonists of CB are
useful in regenerative medicine, for example to promote the expansion of progenitor cells for the
replacement of neurons lost during injury or disease, such as Alzheimer's Disease, stroke-
induced damage, dementia, amyotrophic lateral sclerosis (ALS) and Parkinson’s Disease.
8. CERTAIN EMBODIMENTS.
One aspect of the present invention relates to methods for the treatment of a
cannabinoid receptor-mediated disorder in an individual, comprising administering to the
individual in need thereof, a therapeutically effective amount of an anhydrous crystalline form
as described herein or a pharmaceutical composition thereof.
One aspect of the present invention relates to methods for the treatment of a CB
receptor-mediated disorder in an individual, comprising administering to the individual in need
thereof, a therapeutically effective amount of an anhydrous crystalline form as described herein
or a pharmaceutical composition thereof.
One aspect of the present invention relates to methods for the treatment of pain in an
individual, comprising administering to the individual in need thereof, a therapeutically effective
amount of an anhydrous crystalline form as described herein or a pharmaceutical composition
thereof.
One aspect of the present invention relates to methods for the treatment of bone pain in
an individual, comprising administering to the individual in need thereof, a therapeutically
effective amount of an anhydrous crystalline form as described herein or a pharmaceutical
composition thereof.
One aspect of the present invention relates to methods for the treatment of joint pain in
an individual, comprising administering to the individual in need thereof, a therapeutically
effective amount of an anhydrous crystalline form as described herein or a pharmaceutical
composition thereof.
One aspect of the present invention relates to methods for the treatment of pain
associated with osteoarthritis in an individual, comprising administering to the individual in
need thereof, a therapeutically effective amount of an anhydrous crystalline form as described
herein or a pharmaceutical composition thereof.
One aspect of the present invention relates to methods for the treatment of osteoarthritis
in an individual, comprising administering to the individual in need thereof, a therapeutically
effective amount of an anhydrous crystalline form as described herein or a pharmaceutical
composition thereof.
One aspect of the present invention relates to methods for the treatment of osteoporosis
in an individual, comprising administering to the individual in need thereof, a therapeutically
effective amount of an anhydrous crystalline form as described herein or a pharmaceutical
composition thereof.
One aspect of the present invention relates to methods for the treatment of hyperalgesia
in an individual, comprising administering to the individual in need thereof, a therapeutically
effective amount of an anhydrous crystalline form as described herein or a pharmaceutical
composition thereof.
One aspect of the present invention relates to methods for the treatment of allodynia in
an individual, comprising administering to the individual in need thereof, a therapeutically
effective amount of an anhydrous crystalline form as described herein or a pharmaceutical
composition thereof.
One aspect of the present invention relates to methods for the treatment of inflammatory
pain in an individual, comprising administering to the individual in need thereof, a
therapeutically effective amount of an anhydrous crystalline form as described herein or a
pharmaceutical composition thereof.
One aspect of the present invention relates to methods for the treatment of inflammatory
hyperalgesia in an individual, comprising administering to the individual in need thereof, a
therapeutically effective amount of an anhydrous crystalline form as described herein or a
pharmaceutical composition thereof.
One aspect of the present invention relates to methods for the treatment of neuropathic
pain in an individual, comprising administering to the individual in need thereof, a
therapeutically effective amount of an anhydrous crystalline form as described herein or a
pharmaceutical composition thereof.
One aspect of the present invention relates to methods for the treatment of neuropathic
hyperalgesia in an individual, comprising administering to the individual in need thereof, a
therapeutically effective amount of an anhydrous crystalline form as described herein or a
pharmaceutical composition thereof.
One aspect of the present invention relates to methods for the treatment of acute
nociception in an individual, comprising administering to the individual in need thereof, a
therapeutically effective amount of an anhydrous crystalline form as described herein or a
pharmaceutical composition thereof.
One aspect of the present invention relates to methods for the treatment of muscle pain
in an individual, comprising administering to the individual in need thereof, a therapeutically
effective amount of an anhydrous crystalline form as described herein or a pharmaceutical
composition thereof.
One aspect of the present invention relates to methods for the treatment of dental pain in
an individual, comprising administering to the individual in need thereof, a therapeutically
effective amount of an anhydrous crystalline form as described herein or a pharmaceutical
composition thereof.
One aspect of the present invention relates to methods for the treatment of migraine and
other headache pain in an individual, comprising administering to the individual in need thereof,
a therapeutically effective amount of an anhydrous crystalline form as described herein or a
pharmaceutical composition thereof.
One aspect of the present invention relates to methods for the treatment of pain that
occurs as an adverse effect of therapeutics in an individual, comprising administering to the
individual in need thereof, a therapeutically effective amount of an anhydrous crystalline form
as described herein or a pharmaceutical composition thereof.
One aspect of the present invention relates to methods for the treatment of pain
associated with a disorder selected from: cancer, multiple sclerosis, allergic reactions, nephritic
syndrome, scleroderma, thyroiditis, diabetic neuropathy, fibromyalgia, HIV related-neuropathy,
sciatica, and autoimmune conditions, in an individual, comprising administering to the
individual in need thereof, a therapeutically effective amount of an anhydrous crystalline form
as described herein or a pharmaceutical composition thereof.
One aspect of the present invention relates to methods for the treatment of multiple
sclerosis-associated spasticity in an individual, comprising administering to the individual in
need thereof, a therapeutically effective amount of an anhydrous crystalline form as described
herein or a pharmaceutical composition thereof.
One aspect of the present invention relates to methods for the treatment of autoimmune
disorders in an individual, comprising administering to the individual in need thereof, a
therapeutically effective amount of an anhydrous crystalline form as described herein or a
pharmaceutical composition thereof.
One aspect of the present invention relates to methods for the treatment of an
autoimmune disorder selected from the group consisting of: multiple sclerosis, Guillan-Barré
syndrome, polyradiculoneuropathy, chronic inflammatory demyelination, rheumatoid arthritis,
psoriatic arthritis, ankylosing spondylarthritis, and reactive arthritis, in an individual, comprising
administering to the individual in need thereof, a therapeutically effective amount of an
anhydrous crystalline form as described herein or a pharmaceutical composition thereof.
One aspect of the present invention relates to methods for the treatment of allergic
reactions in an individual, comprising administering to the individual in need thereof, a
therapeutically effective amount of an anhydrous crystalline form as described herein or a
pharmaceutical composition thereof.
One aspect of the present invention relates to methods for the treatment of an allergic
reaction associated with a disorder selected from: atopic dermatitis, pruritis, urticaria, asthma,
conjunctivitis, allergic rhinitis, and anaphylaxis in an individual, comprising administering to
the individual in need thereof, a therapeutically effective amount of an anhydrous crystalline
form as described herein or a pharmaceutical composition thereof.
One aspect of the present invention relates to methods for the treatment of CNS
inflammation in an individual, comprising administering to the individual in need thereof, a
therapeutically effective amount of an anhydrous crystalline form as described herein or a
pharmaceutical composition thereof.
One aspect of the present invention relates to methods for the treatment of CNS
inflammation associated with a disorder selected from: Alzheimer's disease, stroke, dementia,
amyotrophic lateral sclerosis, and human immunodeficiency virus, in an individual, comprising
administering to the individual in need thereof, a therapeutically effective amount of an
anhydrous crystalline form as described herein or a pharmaceutical composition thereof.
One aspect of the present invention relates to methods for the treatment of
atherosclerosis in an individual, comprising administering to the individual in need thereof, a
therapeutically effective amount of an anhydrous crystalline form as described herein or a
pharmaceutical composition thereof.
One aspect of the present invention relates to methods for the treatment of undesired
immune cell activity and inflammation associated with a disorder selected from: osteoarthritis,
anaphylaxis, Behcet's disease, graft rejection, vasculitis, gout, spondylitis, viral disease,
bacterial disease, lupus, inflammatory bowel disease, autoimmune hepatitis, and type 1 diabetes
mellitus, in an individual, comprising administering to the individual in need thereof, a
therapeutically effective amount of an anhydrous crystalline form as described herein or a
pharmaceutical composition thereof.
One aspect of the present invention relates to methods for the treatment of age-related
macular degeneration in an individual, comprising administering to the individual in need
thereof, a therapeutically effective amount of an anhydrous crystalline form as described herein
or a pharmaceutical composition thereof.
One aspect of the present invention relates to methods for the treatment of cough in an
individual, comprising administering to the individual in need thereof, a therapeutically effective
amount of an anhydrous crystalline form as described herein or a pharmaceutical composition
thereof.
One aspect of the present invention relates to methods for the treatment of leukemia in
an individual, comprising administering to the individual in need thereof, a therapeutically
effective amount of an anhydrous crystalline form as described herein or a pharmaceutical
composition thereof.
One aspect of the present invention relates to methods for the treatment of lymphoma in
an individual, comprising administering to the individual in need thereof, a therapeutically
effective amount of an anhydrous crystalline form as described herein or a pharmaceutical
composition thereof.
One aspect of the present invention relates to methods for the treatment of CNS tumors
in an individual, comprising administering to the individual in need thereof, a therapeutically
effective amount of an anhydrous crystalline form as described herein or a pharmaceutical
composition thereof.
One aspect of the present invention relates to methods for the treatment of prostate
cancer in an individual, comprising administering to the individual in need thereof, a
therapeutically effective amount of an anhydrous crystalline form as described herein or a
pharmaceutical composition thereof.
One aspect of the present invention relates to methods for the treatment of Alzheimer's
disease in an individual, comprising administering to the individual in need thereof, a
therapeutically effective amount of an anhydrous crystalline form as described herein or a
pharmaceutical composition thereof.
One aspect of the present invention relates to methods for the treatment of stroke-
induced damage in an individual, comprising administering to the individual in need thereof, a
therapeutically effective amount of an anhydrous crystalline form as described herein or a
pharmaceutical composition thereof.
One aspect of the present invention relates to methods for the treatment of dementia in
an individual, comprising administering to the individual in need thereof, a therapeutically
effective amount of an anhydrous crystalline form as described herein or a pharmaceutical
composition thereof.
One aspect of the present invention relates to methods for the treatment of amyotrophic
lateral sclerosis in an individual, comprising administering to the individual in need thereof, a
therapeutically effective amount of an anhydrous crystalline form as described herein or a
pharmaceutical composition thereof.
One aspect of the present invention relates to methods for the treatment of Parkinson's
disease in an individual, comprising administering to the individual in need thereof, a
therapeutically effective amount of an anhydrous crystalline form as described herein or a
pharmaceutical composition thereof.
One aspect of the present invention relates to the use of an anhydrous crystalline form as
described herein, in the manufacture of a medicament for the treatment of a cannabinoid
receptor-mediated disorder.
One aspect of the present invention relates to the use of an anhydrous crystalline form as
described herein, in the manufacture of a medicament for the treatment of a CB receptor-
mediated disorder.
One aspect of the present invention relates to the use of an anhydrous crystalline form as
described herein, in the manufacture of a medicament for the treatment of pain.
One aspect of the present invention relates to the use of an anhydrous crystalline form as
described herein, in the manufacture of a medicament for the treatment of bone pain.
One aspect of the present invention relates to the use of an anhydrous crystalline form as
described herein, in the manufacture of a medicament for the treatment of joint pain.
One aspect of the present invention relates to the use of an anhydrous crystalline form as
described herein, in the manufacture of a medicament for the treatment of pain associated with
osteoarthritis.
One aspect of the present invention relates to the use of an anhydrous crystalline form as
described herein, in the manufacture of a medicament for the treatment of osteoarthritis.
One aspect of the present invention relates to the use of an anhydrous crystalline form as
described herein, in the manufacture of a medicament for the treatment of osteoporosis.
One aspect of the present invention relates to the use of an anhydrous crystalline form as
described herein, in the manufacture of a medicament for the treatment of hyperalgesia.
One aspect of the present invention relates to the use of an anhydrous crystalline form as
described herein, in the manufacture of a medicament for the treatment of allodynia.
One aspect of the present invention relates to the use of an anhydrous crystalline form as
described herein, in the manufacture of a medicament for the treatment of inflammatory pain.
One aspect of the present invention relates to the use of an anhydrous crystalline form as
described herein, in the manufacture of a medicament for the treatment of inflammatory
hyperalgesia.
One aspect of the present invention relates to the use of an anhydrous crystalline form as
described herein, in the manufacture of a medicament for the treatment of neuropathic pain.
One aspect of the present invention relates to the use of an anhydrous crystalline form as
described herein, in the manufacture of a medicament for the treatment of neuropathic
hyperalgesia.
One aspect of the present invention relates to the use of an anhydrous crystalline form as
described herein, in the manufacture of a medicament for the treatment of acute nociception.
One aspect of the present invention relates to the use of an anhydrous crystalline form as
described herein, in the manufacture of a medicament for the treatment of muscle pain.
One aspect of the present invention relates to the use of an anhydrous crystalline form as
described herein, in the manufacture of a medicament for the treatment of dental pain.
One aspect of the present invention relates to the use of an anhydrous crystalline form as
described herein, in the manufacture of a medicament for the treatment of migraine and other
headache pain.
One aspect of the present invention relates to the use of an anhydrous crystalline form as
described herein, in the manufacture of a medicament for the treatment of pain that occurs as an
adverse effect of therapeutics.
One aspect of the present invention relates to the use of an anhydrous crystalline form as
described herein, in the manufacture of a medicament for the treatment of pain associated with a
disorder selected from: cancer, multiple sclerosis, allergic reactions, nephritic syndrome,
scleroderma, thyroiditis, diabetic neuropathy, fibromyalgia, HIV related-neuropathy, sciatica,
and autoimmune conditions.
One aspect of the present invention relates to the use of an anhydrous crystalline form as
described herein, in the manufacture of a medicament for the treatment of multiple sclerosis-
associated spasticity.
One aspect of the present invention relates to the use of an anhydrous crystalline form as
described herein, in the manufacture of a medicament for the treatment of autoimmune
disorders.
One aspect of the present invention relates to the use of an anhydrous crystalline form as
described herein, in the manufacture of a medicament for the treatment of an autoimmune
disorder selected from the group consisting of: multiple sclerosis, Guillan-Barré syndrome,
polyradiculoneuropathy, chronic inflammatory demyelination, rheumatoid arthritis, psoriatic
arthritis, ankylosing spondylarthritis, and reactive arthritis.
One aspect of the present invention relates to the use of an anhydrous crystalline form as
described herein, in the manufacture of a medicament for the treatment of allergic reactions.
One aspect of the present invention relates to the use of an anhydrous crystalline form as
described herein, in the manufacture of a medicament for the treatment of an allergic reaction
associated with a disorder selected from: atopic dermatitis, pruritis, urticaria, asthma,
conjunctivitis, allergic rhinitis, and anaphylaxis.
One aspect of the present invention relates to the use of an anhydrous crystalline form as
described herein, in the manufacture of a medicament for the treatment of CNS inflammation.
One aspect of the present invention relates to the use of an anhydrous crystalline form as
described herein, in the manufacture of a medicament for the treatment of CNS inflammation
associated with a disorder selected from: Alzheimer's disease, stroke, dementia, amyotrophic
lateral sclerosis, and human immunodeficiency virus.
One aspect of the present invention relates to the use of an anhydrous crystalline form as
described herein, in the manufacture of a medicament for the treatment of atherosclerosis.
One aspect of the present invention relates to the use of an anhydrous crystalline form as
described herein, in the manufacture of a medicament for the treatment of undesired immune
cell activity and inflammation associated with a disorder selected from: osteoarthritis,
anaphylaxis, Behcet's disease, graft rejection, vasculitis, gout, spondylitis, viral disease,
bacterial disease, lupus, inflammatory bowel disease, autoimmune hepatitis, and type 1 diabetes
mellitus.
One aspect of the present invention relates to the use of an anhydrous crystalline form as
described herein, in the manufacture of a medicament for the treatment of age-related macular
degeneration.
One aspect of the present invention relates to the use of an anhydrous crystalline form as
described herein, in the manufacture of a medicament for the treatment of cough.
One aspect of the present invention relates to the use of an anhydrous crystalline form as
described herein, in the manufacture of a medicament for the treatment of leukemia.
One aspect of the present invention relates to the use of an anhydrous crystalline form as
described herein, in the manufacture of a medicament for the treatment of lymphoma.
One aspect of the present invention relates to the use of an anhydrous crystalline form as
described herein, in the manufacture of a medicament for the treatment of CNS tumors.
One aspect of the present invention relates to the use of an anhydrous crystalline form as
described herein, in the manufacture of a medicament for the treatment of prostate cancer.
One aspect of the present invention relates to the use of an anhydrous crystalline form as
described herein, in the manufacture of a medicament for the treatment of Alzheimer's disease.
One aspect of the present invention relates to the use of an anhydrous crystalline form as
described herein, in the manufacture of a medicament for the treatment of stroke-induced
damage.
One aspect of the present invention relates to the use of an anhydrous crystalline form as
described herein, in the manufacture of a medicament for the treatment of dementia.
One aspect of the present invention relates to the use of an anhydrous crystalline form as
described herein, in the manufacture of a medicament for the treatment of amyotrophic lateral
sclerosis.
One aspect of the present invention relates to the use of an anhydrous crystalline form as
described herein, in the manufacture of a medicament for the treatment of Parkinson's disease.
One aspect of the present invention relates to an anhydrous crystalline form as described
herein, for use in a method of treatment of the human or animal body by therapy.
One aspect of the present invention relates to an anhydrous crystalline form as described
herein, for use in a method of treatment of a cannabinoid receptor-mediated disorder.
One aspect of the present invention relates to an anhydrous crystalline form as described
herein, for use in a method of treatment of a CB receptor-mediated disorder.
One aspect of the present invention relates to an anhydrous crystalline form as described
herein, for use in a method of treatment of pain.
One aspect of the present invention relates to an anhydrous crystalline form as described
herein, for use in a method of treatment of bone pain.
One aspect of the present invention relates to an anhydrous crystalline form as described
herein, for use in a method of treatment of joint pain.
One aspect of the present invention relates to an anhydrous crystalline form as described
herein, for use in a method of treatment of pain associated with osteoarthritis.
One aspect of the present invention relates to an anhydrous crystalline form as described
herein, for use in a method of treatment of osteoarthritis.
One aspect of the present invention relates to an anhydrous crystalline form as described
herein, for use in a method of treatment of osteoporosis.
One aspect of the present invention relates to an anhydrous crystalline form as described
herein, for use in a method of treatment of hyperalgesia.
One aspect of the present invention relates to an anhydrous crystalline form as described
herein, for use in a method of treatment of allodynia.
One aspect of the present invention relates to an anhydrous crystalline form as described
herein, for use in a method of treatment of inflammatory pain.
One aspect of the present invention relates to an anhydrous crystalline form as described
herein, for use in a method of treatment of inflammatory hyperalgesia.
One aspect of the present invention relates to an anhydrous crystalline form as described
herein, for use in a method of treatment of neuropathic pain.
One aspect of the present invention relates to an anhydrous crystalline form as described
herein, for use in a method of treatment of neuropathic hyperalgesia.
One aspect of the present invention relates to an anhydrous crystalline form as described
herein, for use in a method of treatment of acute nociception.
One aspect of the present invention relates to an anhydrous crystalline form as described
herein, for use in a method of treatment of muscle pain.
One aspect of the present invention relates to an anhydrous crystalline form as described
herein, for use in a method of treatment of dental pain.
One aspect of the present invention relates to an anhydrous crystalline form as described
herein, for use in a method of treatment of migraine and other headache pain.
One aspect of the present invention relates to an anhydrous crystalline form as described
herein, for use in a method of treatment of pain that occurs as an adverse effect of therapeutics.
One aspect of the present invention relates to an anhydrous crystalline form as described
herein, for use in a method of treatment of pain associated with a disorder selected from: cancer,
multiple sclerosis, allergic reactions, nephritic syndrome, scleroderma, thyroiditis, diabetic
neuropathy, fibromyalgia, HIV related-neuropathy, sciatica, and autoimmune conditions.
One aspect of the present invention relates to an anhydrous crystalline form as described
herein, for use in a method of treatment of multiple sclerosis-associated spasticity.
One aspect of the present invention relates to an anhydrous crystalline form as described
herein, for use in a method of treatment of autoimmune disorders.
One aspect of the present invention relates to an anhydrous crystalline form as described
herein, for use in a method of treatment of an autoimmune disorder selected from the group
consisting of: multiple sclerosis, Guillan-Barré syndrome, polyradiculoneuropathy, chronic
inflammatory demyelination, rheumatoid arthritis, psoriatic arthritis, ankylosing
spondylarthritis, and reactive arthritis.
One aspect of the present invention relates to an anhydrous crystalline form as described
herein, for use in a method of treatment of allergic reactions.
One aspect of the present invention relates to an anhydrous crystalline form as described
herein, for use in a method of treatment of an allergic reaction associated with a disorder
selected from: atopic dermatitis, pruritis, urticaria, asthma, conjunctivitis, allergic rhinitis, and
anaphylaxis.
One aspect of the present invention relates to an anhydrous crystalline form as described
herein, for use in a method of treatment of CNS inflammation.
One aspect of the present invention relates to an anhydrous crystalline form as described
herein, for use in a method of treatment of CNS inflammation associated with a disorder
selected from: Alzheimer's disease, stroke, dementia, amyotrophic lateral sclerosis, and human
immunodeficiency virus.
One aspect of the present invention relates to an anhydrous crystalline form as described
herein, for use in a method of treatment of atherosclerosis.
One aspect of the present invention relates to an anhydrous crystalline form as described
herein, for use in a method of treatment of undesired immune cell activity and inflammation
associated with a disorder selected from: osteoarthritis, anaphylaxis, Behcet's disease, graft
rejection, vasculitis, gout, spondylitis, viral disease, bacterial disease, lupus, inflammatory
bowel disease, autoimmune hepatitis, and type 1 diabetes mellitus.
One aspect of the present invention relates to an anhydrous crystalline form as described
herein, for use in a method of treatment of age-related macular degeneration.
One aspect of the present invention relates to an anhydrous crystalline form as described
herein, for use in a method of treatment of cough.
One aspect of the present invention relates to an anhydrous crystalline form as described
herein, for use in a method of treatment of leukemia.
One aspect of the present invention relates to an anhydrous crystalline form as described
herein, for use in a method of treatment of lymphoma.
One aspect of the present invention relates to an anhydrous crystalline form as described
herein, for use in a method of treatment of CNS tumors.
One aspect of the present invention relates to an anhydrous crystalline form as described
herein, for use in a method of treatment of prostate cancer.
One aspect of the present invention relates to an anhydrous crystalline form as described
herein, for use in a method of treatment of Alzheimer's disease.
One aspect of the present invention relates to an anhydrous crystalline form as described
herein, for use in a method of treatment of stroke-induced damage.
One aspect of the present invention relates to an anhydrous crystalline form as described
herein, for use in a method of treatment of dementia.
One aspect of the present invention relates to an anhydrous crystalline form as described
herein, for use in a method of treatment of amyotrophic lateral sclerosis.
One aspect of the present invention relates to an anhydrous crystalline form as described
herein, for use in a method of treatment of Parkinson's disease.
PHARMACEUTICAL COMPOSITIONS AND DOSAGE FORMS
One aspect of the present invention relates to compositions comprising an anhydrous
crystalline form of (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-
cyclopropa[a]pentalenecarboxylic acid ((S)hydroxymethyl-2,2-dimethyl-propyl)-amide as
described herein.
One aspect of the present invention relates to compositions comprising an anhydrous
crystalline form of (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-
cyclopropa[a]pentalenecarboxylic acid ((S)hydroxymethyl-2,2-dimethyl-propyl)-amide as
described herein, and a pharmaceutically acceptable carrier.
One aspect of the present invention relates to pharmaceutical compositions comprising
an anhydrous crystalline form of (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-
diaza-cyclopropa[a]pentalenecarboxylic acid ((S)hydroxymethyl-2,2-dimethyl-propyl)-
amide as described herein, and a pharmaceutically acceptable carrier.
One aspect of the present invention relates to dosage forms comprising an anhydrous
crystalline form of (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-
cyclopropa[a]pentalenecarboxylic acid ((S)hydroxymethyl-2,2-dimethyl-propyl)-amide as
described herein, and a pharmaceutically acceptable carrier.
One aspect of the present invention relates to processes for preparing pharmaceutical
compositions comprising the steps of:
1) preparing an anhydrous crystalline form of (1aS,5aS)(4-oxy-pyrazinyl)-
1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S)
hydroxymethyl-2,2-dimethyl-propyl)-amide according to any of the processes decribed herein;
2) admixing said anhydrous crystalline form of (1aS,5aS)(4-oxy-pyrazinyl)-
1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S)
hydroxymethyl-2,2-dimethyl-propyl)-amide with a phamaceutically acceptable carrier.
One aspect of the present invention relates to processes for preparing a dosage form
comprising the steps of:
1) preparing an anhydrous crystalline form of (1aS,5aS)(4-oxy-pyrazinyl)-
1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S)
hydroxymethyl-2,2-dimethyl-propyl)-amide according to any of the processes decribed herein;
and
2) admixing said anhydrous crystalline form of (1aS,5aS)(4-oxy-pyrazinyl)-
1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S)
hydroxymethyl-2,2-dimethyl-propyl)-amide with a phamaceutically acceptable carrier.
One aspect of the present invention relates to compositions comprising a solvate as
described herein.
Some embodiments of the present invention include a method of producing a
pharmaceutical composition comprising admixing at least one compound according to any of
the compound embodiments disclosed herein and a pharmaceutically acceptable carrier.
Formulations may be prepared by any suitable method, typically by uniformly mixing
the active compound(s) with liquids or finely divided solid carriers, or both, in the required
proportions and then, if necessary, forming the resulting mixture into a desired shape or
dispensing into a desired vial or ampule.
Conventional excipients, such as binding agents, fillers, acceptable wetting agents,
tabletting lubricants and disintegrants may be used in tablets and capsules for oral
administration. Liquid preparations for oral administration may be in the form of solutions,
emulsions, aqueous or oily suspensions and syrups. Alternatively, the oral preparations may be
in the form of dry powder that can be reconstituted with water or another suitable liquid vehicle
before use. Additional additives such as suspending or emulsifying agents, non-aqueous vehicles
(including edible oils), preservatives and flavorings and colorants may be added to the liquid
preparations. Parenteral dosage forms may be prepared by dissolving the compound of the
invention in a suitable liquid vehicle and filter sterilizing the solution before filling and sealing
an appropriate vial or ampule. These are just a few examples of the many appropriate methods
well known in the art for preparing dosage forms.
A compound of the present invention can be formulated into pharmaceutical
compositions using techniques well known to those in the art. Suitable pharmaceutically-
acceptable carriers, outside those mentioned herein, are known in the art; for example, see
Remington, The Science and Practice of Pharmacy, 20 Edition, 2000, Lippincott Williams &
Wilkins, (Editors: Gennaro et al.)
While it is possible that, for use in the prophylaxis or treatment, a compound of the
invention may, in an alternative use, be administered as a raw or pure chemical, it is preferable
however to present the compound or active ingredient as a pharmaceutical formulation or
composition further comprising a pharmaceutically acceptable carrier.
Pharmaceutical formulations include those suitable for oral, rectal, nasal, topical
(including buccal and sub-lingual), vaginal or parenteral (including intramuscular, sub-
cutaneous and intravenous) administration or in a form suitable for administration by inhalation,
insufflation or by a transdermal patch. Transdermal patches dispense a drug at a controlled rate
by presenting the drug for absorption in an efficient manner with minimal degradation of the
drug. Typically, transdermal patches comprise an impermeable backing layer, a single pressure
sensitive adhesive and a removable protective layer with a release liner. One of ordinary skill in
the art will understand and appreciate the techniques appropriate for manufacturing a desired
efficacious transdermal patch based upon the needs of the artisan.
The compounds of the invention, together with a conventional adjuvant, carrier, or
diluent, may thus be placed into the form of pharmaceutical formulations and unit dosage forms
thereof and in such form may be employed as solids, such as tablets or filled capsules, or liquids
such as solutions, suspensions, emulsions, elixirs, gels or capsules filled with the same, all for
oral use, in the form of suppositories for rectal administration; or in the form of sterile injectable
solutions for parenteral (including subcutaneous) use. Such pharmaceutical compositions and
unit dosage forms thereof may comprise conventional ingredients in conventional proportions,
with or without additional active compounds or principles and such unit dosage forms may
contain any suitable effective amount of the active ingredient commensurate with the intended
daily dosage range to be employed.
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 capsules, tablets, powders, granules or a suspension, with
conventional additives such as lactose, mannitol, corn starch or potato starch; with binders such
as crystalline cellulose, cellulose derivatives, acacia, corn starch or gelatins; with disintegrators
such as corn starch, potato starch or sodium carboxymethyl-cellulose; and with lubricants such
as talc or magnesium stearate. 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
pharmaceutically acceptable carrier.
Compounds of the present invention or a solvate, hydrate or physiologically functional
derivative thereof can be used as active ingredients in pharmaceutical compositions, specifically
as cannabinoid receptor modulators. By the term “active ingredient” is defined in the context of
a “pharmaceutical composition” and refers to a component of a pharmaceutical composition that
provides the primary pharmacological effect, as opposed to an “inactive ingredient” which
would generally be recognized as providing no pharmaceutical benefit.
The dose when using the compounds of the present invention can vary within wide
limits and as is customary and is known to the physician, it is to be tailored to the individual
conditions in each individual case. It depends, for example, on the nature and severity of the
illness to be treated, on the condition of the patient, on the compound employed or on whether
an acute or chronic disease state is treated or prophylaxis conducted or on whether further active
compounds are administered in addition to the compounds of the present invention.
Representative doses of the present invention include, but not limited to, about 0.001 mg to
about 5000 mg, about 0.001 mg to about 2500 mg, about 0.001 mg to about 1000 mg, 0.001 mg
to about 500 mg, 0.001 mg to about 250 mg, about 0.001 mg to 100 mg, about 0.001 mg to
about 50 mg and about 0.001 mg to about 25 mg. Multiple doses may be administered during
the day, especially when relatively large amounts are deemed to be needed, for example 2, 3 or
4 doses. Depending on the individual and as deemed appropriate from the patient's physician or
caregiver it may be necessary to deviate upward or downward from the doses described herein.
The amount of active ingredient, or an active salt or derivative thereof, required for use
in treatment will vary not only with the particular salt selected but also with the route of
administration, the nature of the condition being treated and the age and condition of the patient
and will ultimately be at the discretion of the attendant physician or clinician. In general, one
skilled in the art understands how to extrapolate in vivo data obtained in a model system,
typically an animal model, to another, such as a human. In some circumstances, these
extrapolations may merely be based on the weight of the animal model in comparison to
another, such as a mammal, preferably a human, however, more often, these extrapolations are
not simply based on weights, but rather incorporate a variety of factors. Representative factors
include the type, age, weight, sex, diet and medical condition of the patient, the severity of the
disease, the route of administration, pharmacological considerations such as the activity,
efficacy, pharmacokinetic and toxicology profiles of the particular compound employed,
whether a drug delivery system is utilized, on whether an acute or chronic disease state is being
treated or prophylaxis conducted or on whether further active compounds are administered in
addition to the compounds of the present invention and as part of a drug combination. The
dosage regimen for treating a disease condition with the compounds and/or compositions of this
invention is selected in accordance with a variety factors as cited above. Thus, the actual dosage
regimen employed may vary widely and therefore may deviate from a preferred dosage regimen
and one skilled in the art will recognize that dosage and dosage regimen outside these typical
ranges can be tested and, where appropriate, may be used in the methods of this invention.
The desired dose may conveniently be presented in a single dose or as divided doses
administered at appropriate intervals, for example, as two, three, four or more sub-doses per day.
The sub-dose itself may be further divided, e.g., into a number of discrete loosely spaced
administrations. The daily dose can be divided, especially when relatively large amounts are
administered as deemed appropriate, into several, for example 2, 3 or 4 part administrations. If
appropriate, depending on individual behavior, it may be necessary to deviate upward or
downward from the daily dose indicated.
The compounds of the present invention can be administrated in a wide variety of oral
and parenteral dosage forms. It will be obvious to those skilled in the art that the following
dosage forms may comprise, as the active component, either a compound of the invention or a
pharmaceutically acceptable salt, solvate or hydrate of a compound of the invention.
For preparing pharmaceutical compositions from the compounds of the present
invention, the selection of a suitable pharmaceutically acceptable carrier can be either solid,
liquid or a mixture of both. Solid form preparations include powders, tablets, pills, capsules,
cachets, suppositories and dispersible granules. A solid carrier can be one or more substances
which may also act as diluents, flavoring agents, solubilizers, lubricants, suspending agents,
binders, preservatives, tablet disintegrating agents, or an encapsulating material.
In powders, the carrier is a finely divided solid which is in a mixture with the finely
divided active component.
In tablets, the active component is mixed with the carrier having the necessary binding
capacity in suitable proportions and compacted to the desire shape and size.
The powders and tablets may contain varying percentage amounts of the active compound. A
representative amount in a powder or tablet may contain from 0.5 to about 90 percent of the
active compound; however, an artisan would know when amounts outside of this range are
necessary. Suitable carriers for powders and tablets are magnesium carbonate, magnesium
stearate, talc, sugar, lactose, pectin, dextrin, starch, gelatin, tragacanth, methylcellulose, sodium
carboxymethylcellulose, a low melting wax, cocoa butter and the like. The term “preparation”
includes the formulation of the active compound with encapsulating material as carrier
providing a capsule in which the active component, with or without carriers, is surrounded by a
carrier, which is thus in association with it. Similarly, cachets and lozenges are included.
Tablets, powders, capsules, pills, cachets and lozenges can be used as solid forms suitable for
oral administration.
For preparing suppositories, a low melting wax, such as an admixture of fatty acid
glycerides or cocoa butter, is first melted and the active component is dispersed homogeneously
therein, as by stirring. The molten homogenous mixture is then poured into convenient sized
molds, allowed to cool and thereby to solidify.
Formulations suitable for vaginal administration may be presented as pessaries,
tampons, creams, gels, pastes, foams or sprays containing in addition to the active ingredient
such carriers as are known in the art to be appropriate.
Liquid form preparations include solutions, suspensions and emulsions, for example,
water or water-propylene glycol solutions. For example, parenteral injection liquid preparations
can be formulated as solutions in aqueous polyethylene glycol solution. Injectable preparations,
for example, sterile injectable aqueous or oleaginous suspensions may be formulated according
to the known art using suitable dispersing or wetting agents and suspending agents. The sterile
injectable preparation may also be a sterile injectable solution or suspension in a nontoxic
parenterally acceptable diluent or solvent, for example, as a solution in 1,3-butanediol. Among
the acceptable vehicles and solvents that may be employed are water, Ringer's solution and
isotonic sodium chloride solution. In addition, sterile, fixed oils are conventionally employed as
a solvent or suspending medium. For this purpose any bland fixed oil may be employed
including synthetic mono- or diglycerides. In addition, fatty acids such as oleic acid find use in
the preparation of injectables.
The compounds according to the present invention may thus be formulated for
parenteral administration (e.g. by injection, for example bolus injection or continuous infusion)
and may be presented in unit dosage form in ampoules, pre-filled syringes, small volume
infusion or in multi-dose containers with an added preservative. The pharmaceutical
compositions may take such forms as suspensions, solutions, or emulsions in oily or aqueous
vehicles and may contain formulatory agents such as suspending, stabilizing and/or dispersing
agents. Alternatively, the active ingredient may be in powder form, obtained by aseptic isolation
of sterile solid or by lyophilization from solution, for constitution with a suitable vehicle, e.g.
sterile, pyrogen-free water, before use.
Aqueous formulations suitable for oral use can be prepared by dissolving or suspending
the active component in water and adding suitable colorants, flavors, stabilizing and thickening
agents, as desired.
Aqueous suspensions suitable for oral use can be made by dispersing the finely divided
active component in water with viscous material, such as natural or synthetic gums, resins,
methylcellulose, sodium carboxymethylcellulose, or other well-known suspending agents.
Also included are solid form preparations which can be converted, shortly before use, to
liquid form preparations for oral administration. Such liquid forms include solutions,
suspensions and emulsions. These preparations may contain, in addition to the active
component, colorants, flavors, stabilizers, buffers, artificial and natural sweeteners, dispersants,
thickeners, solubilizing agents and the like.
For topical administration to the epidermis the compounds according to the invention
may be formulated as ointments, creams or lotions, or as a transdermal patch.
Ointments and creams may, for example, be formulated with an aqueous or oily base
with the addition of suitable thickening and/or gelling agents. Lotions may be formulated with
an aqueous or oily base and will in general also contain one or more emulsifying agents,
stabilizing agents, dispersing agents, suspending agents, thickening agents, or coloring agents.
Formulations suitable for topical administration in the mouth include lozenges
comprising active agent in a flavored base, usually sucrose and acacia or tragacanth; pastilles
comprising the active ingredient in an inert base such as gelatin and glycerin or sucrose and
acacia; and mouthwashes comprising the active ingredient in a suitable liquid carrier.
Solutions or suspensions are applied directly to the nasal cavity by conventional means,
for example with a dropper, pipette or spray. The formulations may be provided in single or
multi-dose form. In the latter case of a dropper or pipette, this may be achieved by the patient
administering an appropriate, predetermined volume of the solution or suspension. In the case of
a spray, this may be achieved for example by means of a metering atomizing spray pump.
Administration to the respiratory tract may also be achieved by means of an aerosol
formulation in which the active ingredient is provided in a pressurized pack with a suitable
propellant. If the compounds of the present invention or pharmaceutical compositions
comprising them are administered as aerosols, for example as nasal aerosols or by inhalation,
this can be carried out, for example, using a spray, a nebulizer, a pump nebulizer, an inhalation
apparatus, a metered inhaler or a dry powder inhaler. Pharmaceutical forms for administration of
the compounds of the present invention as an aerosol can be prepared by processes well known
to the person skilled in the art. For their preparation, for example, solutions or dispersions of the
compounds of the present invention in water, water/alcohol mixtures or suitable saline solutions
can be employed using customary additives, for example benzyl alcohol or other suitable
preservatives, absorption enhancers for increasing the bioavailability, solubilizers, dispersants
and others and, if appropriate, customary propellants, for example include carbon dioxide,
CFCs, such as, dichlorodifluoromethane, trichlorofluoromethane, or dichlorotetrafluoroethane;
and the like. The aerosol may conveniently also contain a surfactant such as lecithin. The dose
of drug may be controlled by provision of a metered valve.
In formulations for administration to the respiratory tract, including intranasal
formulations, the compound will generally have a small particle size for example of the order of
microns or less. Such a particle size may be obtained by means known in the art, for example
by micronization. When desired, formulations adapted to give sustained release of the active
ingredient may be employed.
Alternatively the active ingredients may be provided in the form of a dry powder, for
example, a powder mix of the compound in a suitable powder base such as lactose, starch, starch
derivatives such as hydroxypropylmethyl cellulose and polyvinylpyrrolidone (PVP).
Conveniently the powder carrier will form a gel in the nasal cavity. The powder composition
may be presented in unit dosage form for example in capsules or cartridges of, e.g., gelatin, or
blister packs from which the powder may be administered by means of an inhaler.
The pharmaceutical preparations are preferably in unit dosage forms. In such form, the
preparation is subdivided into unit doses containing appropriate quantities of the active
component. The unit dosage form can be a packaged preparation, the package containing
discrete quantities of preparation, such as packeted tablets, capsules and powders in vials or
ampoules. Also, the unit dosage form can be a capsule, tablet, cachet, or lozenge itself, or it can
be the appropriate number of any of these in packaged form.
Tablets or capsules for oral administration and liquids for intravenous administration are
preferred compositions.
The compounds according to the invention may optionally exist as pharmaceutically
acceptable salts including pharmaceutically acceptable acid addition salts prepared from
pharmaceutically acceptable non-toxic acids including inorganic and organic acids.
Representative acids include, but are not limited to, acetic, benzenesulfonic, benzoic,
camphorsulfonic, citric, ethenesulfonic, dichloroacetic, formic, fumaric, gluconic, glutamic,
hippuric, hydrobromic, hydrochloric, isethionic, lactic, maleic, malic, mandelic,
methanesulfonic, mucic, nitric, oxalic, pamoic, pantothenic, phosphoric, succinic, sulfiric,
tartaric, oxalic, p-toluenesulfonic and the like. Certain compounds of the present invention
which contain a carboxylic acid functional group may optionally exist as pharmaceutically
acceptable salts containing non-toxic, pharmaceutically acceptable metal cations and cations
derived from organic bases. Representative metals include, but are not limited to, aluminium,
calcium, lithium, magnesium, potassium, sodium, zinc and the like. In some embodiments the
pharmaceutically acceptable metal is sodium. Representative organic bases include, but are not
limited to, benzathine (N ,N -dibenzylethane-1,2-diamine), chloroprocaine (2-
(diethylamino)ethyl 4-(chloroamino)benzoate), choline, diethanolamine, ethylenediamine,
meglumine ((2R,3R,4R,5S)(methylamino)hexane-1,2,3,4,5-pentaol), procaine (2-
(diethylamino)ethyl 4-aminobenzoate), and the like. Certain pharmaceutically acceptable salts
are listed in Berge, et al., Journal of Pharmaceutical Sciences, 66:1-19 (1977).
The acid addition salts may be obtained as the direct products of compound synthesis. In
the alternative, the free base may be dissolved in a suitable solvent containing the appropriate
acid and the salt isolated by evaporating the solvent or otherwise separating the salt and solvent.
The compounds of this invention may form solvates with standard low molecular weight
solvents using methods known to the skilled artisan.
Compounds of the present invention can be converted to “pro-drugs.” The term “pro-
drugs” refers to compounds that have been modified with specific chemical groups known in the
art and when administered into an individual these groups undergo biotransformation to give the
parent compound. Pro-drugs can thus be viewed as compounds of the invention containing one
or more specialized non-toxic protective groups used in a transient manner to alter or to
eliminate a property of the compound. In one general aspect, the “pro-drug” approach is utilized
to facilitate oral absorption. A thorough discussion is provided in T. Higuchi and V. Stella, Pro-
drugs as Novel Delivery Systems Vol. 14 of the A.C.S. Symposium Series; and in Bioreversible
Carriers in Drug Design, ed. Edward B. Roche, American Pharmaceutical Association and
Pergamon Press, 1987, both of which are hereby incorporated by reference in their entirety.
Some embodiments of the present invention include a method of producing a
pharmaceutical composition for “combination-therapy” comprising admixing at least one
compound according to any of the compound embodiments disclosed herein, together with at
least one known pharmaceutical agent as described herein and a pharmaceutically acceptable
carrier.
It is noted that when the cannabinoid receptor modulators are utilized as active
ingredients in a pharmaceutical composition, these are not intended for use only in humans, but
in other non-human mammals as well. Indeed, recent advances in the area of animal health-care
mandate that consideration be given for the use of active agents, such as cannabinoid receptor
modulators, for the treatment of a cannabinoid receptor-associated disease or disorder in
companionship animals (e.g., cats, dogs, etc.) and in livestock animals (e.g., cows, chickens,
etc.) Those of ordinary skill in the art are readily credited with understanding the utility of such
compounds in such settings.
HYDRATES AND SOLVATES
It is understood that when the phrase “pharmaceutically acceptable salts, solvates, and
hydrates” or the phrase “pharmaceutically acceptable salt, solvate, or hydrate” is used when
referring to compounds described herein, it embraces pharmaceutically acceptable solvates
and/or hydrates of the compounds, pharmaceutically acceptable salts of the compounds, as well
as pharmaceutically acceptable solvates and/or hydrates of pharmaceutically acceptable salts of
the compounds. It is also understood that when the phrase “pharmaceutically acceptable solvates
and hydrates” or the phrase “pharmaceutically acceptable solvate or hydrate” is used when
referring to salts described herein, it embraces pharmaceutically acceptable solvates and/or
hydrates of such salts.
It will be apparent to those skilled in the art that the dosage forms described herein may
comprise, as the active component, either a compound described herein or a pharmaceutically
acceptable salt or as a pharmaceutically acceptable solvate or hydrate thereof. Moreover, various
hydrates and solvates of the compounds described herein and their salts will find use as
intermediates in the manufacture of pharmaceutical compositions. Typical procedures for
making and identifying suitable hydrates and solvates, outside those mentioned herein, are well
known to those in the art; see for example, pages 202-209 of K.J. Guillory, “Generation of
Polymorphs, Hydrates, Solvates, and Amorphous Solids,” in: Polymorphism in Pharmaceutical
Solids, ed. Harry G. Britain, Vol. 95, Marcel Dekker, Inc., New York, 1999. Accordingly, one
aspect of the present invention pertains to methods of administering hydrates and solvates of
compounds described herein and/or their pharmaceutical acceptable salts, that can be isolated
and characterized by methods known in the art, such as, thermogravimetric analysis (TGA),
TGA-mass spectroscopy, TGA-Infrared spectroscopy, powder X-ray diffraction (XRPD), Karl
Fisher titration, high resolution X-ray diffraction, and the like. There are several commercial
entities that provide quick and efficient services for identifying solvates and hydrates on a
routine basis. Example companies offering these services include Wilmington PharmaTech
(Wilmington, DE), Avantium Technologies (Amsterdam) and Aptuit (Greenwich, CT).
POLYMORPHS AND PSEUDOPOLYMORPHS
Polymorphism is the ability of a substance to exist as two or more crystalline phases that
have different arrangements and/or conformations of the molecules in the crystal lattice.
Polymorphs show the same properties in the liquid or gaseous state but they behave differently
in the solid state.
Besides single-component polymorphs, drugs can also exist as salts and other
multicomponent crystalline phases. For example, solvates and hydrates may contain an API host
and either solvent or water molecules, respectively, as guests. Analogously, when the guest
compound is a solid at room temperature, the resulting form is often called a cocrystal. Salts,
solvates, hydrates, and cocrystals may show polymorphism as well. Crystalline phases that share
the same API host, but differ with respect to their guests, may be referred to as
pseudopolymorphs of one another.
Solvates contain molecules of the solvent of crystallization in a definite crystal lattice.
Solvates, in which the solvent of crystallization is water, are termed hydrates. Because water is a
constituent of the atmosphere, hydrates of drugs may be formed rather easily.
By way of example, Stahly recently published a polymorph screens of 245 compounds
consisting of a “wide variety of structural types” revealed that about 90% of them exhibited
multiple solid forms. Overall, approximately half the compounds were polymorphic, often
having one to three forms. About one-third of the compounds formed hydrates, and about one-
third formed solvates. Data from cocrystal screens of 64 compounds showed that 60% formed
cocrystals other than hydrates or solvates. (G. P. Stahly, Crystal Growth & Design (2007), 7(6),
1007-1026).
OTHER UTILITIES
Another object of the present invention relates to radio-labeled compounds of the
present invention that would be useful not only in radio-imaging but also in assays, both in vitro
and in vivo, for localizing and quantitating cannabinoid receptors in tissue samples, including
human and for identifying cannabinoid receptor ligands by inhibition binding of a radio-labeled
compound. It is a further object of this invention to develop novel cannabinoid receptor assays
of which comprise such radio-labeled compounds.
The present invention embraces isotopically-labeled crystalline forms of the present
invention. Isotopically or radio-labeled compounds are those which are identical to compounds
disclosed herein, but for the fact that one or more atoms are replaced or substituted by an atom
having an atomic mass or mass number different from the atomic mass or mass number most
commonly found in nature. Suitable radionuclides that may be incorporated in compounds of the
present invention include but are not limited to H (also written as D for deuterium), H (also
11 13 14 13 15 15 17 18 18 35 36 75 76 77 82
written as T for tritium), C, C, C, N, N, O, O, O, F, S, Cl, Br, Br, Br, Br,
123 124 125 131
I, I, I and I. The radionuclide that is incorporated in the instant radio-labeled
compounds will depend on the specific application of that radio-labeled compound. For
example, for in vitro cannabinoid receptor labeling and competition assays, compounds that
3 14 82 125 131 35
incorporate H, C, Br, I, I or S will generally be most useful. For radio-imaging
11 18 125 123 124 131 75 76 77
applications C, F, I, I, I, I, Br, Br or Br will generally be most useful.
It is understood that a “radio-labeled ” or “labeled compound” is a crystalline form of
Compound 1 that has incorporated at least one radionuclide; in some embodiments the
3 14
radionuclide is selected from the group consisting of H, and C.
Certain isotopically-labeled crystalline forms of the present invention are useful in
compound and/or substrate tissue distribution assays. In some embodiments the radionuclide H
and/or C isotopes are useful in these studies. Further, substitution with heavier isotopes such as
deuterium (i.e., H) may afford certain therapeutic advantages resulting from greater metabolic
stability (e.g., increased in vivo half-life or reduced dosage requirements) and hence may be
preferred in some circumstances. Isotopically labeled crystalline forms of the present invention
can generally be prepared by following procedures analogous to those disclosed in the and
Examples infra, by substituting an isotopically labeled reagent for a non-isotopically labeled
reagent. Other synthetic methods that are useful are discussed infra. Moreover, it should be
understood that all of the atoms represented in the compounds of the invention can be either the
most commonly occurring isotope of such atoms or the scarcer radio-isotope or nonradioactive
isotope.
Synthetic methods for incorporating radio-isotopes into organic compounds are
applicable to compounds of the invention and are well known in the art. These synthetic
methods, for example, incorporating activity levels of tritium into target molecules, are as
follows:
A. Catalytic Reduction with Tritium Gas: This procedure normally yields high specific
activity products and requires halogenated or unsaturated precursors.
B. Reduction with Sodium Borohydride [ H]: This procedure is rather inexpensive and
requires precursors containing reducible functional groups such as aldehydes, ketones, lactones,
esters and the like.
C. Reduction with Lithium Aluminum Hydride [ H]: This procedure offers products at
almost theoretical specific activities. It also requires precursors containing reducible functional
groups such as aldehydes, ketones, lactones, esters and the like.
D. Tritium Gas Exposure Labeling: This procedure involves exposing precursors
containing exchangeable protons to tritium gas in the presence of a suitable catalyst.
E. N-Methylation using Methyl Iodide [ H]: This procedure is usually employed to
prepare O-methyl or N-methyl (3H) products by treating appropriate precursors with high
specific activity methyl iodide (3H). This method in general allows for higher specific activity,
such as for example, about 70-90 Ci/mmol.
Synthetic methods for incorporating activity levels of I into target molecules include:
A. Sandmeyer and like reactions: This procedure transforms an aryl amine or a
heteroaryl amine into a diazonium salt, such as a diazonium tetrafluoroborate salt and
125 125
subsequently to I labeled compound using Na I. A represented procedure was reported by
Zhu, G-D. and co-workers in J. Org. Chem., 2002, 67, 943-948.
125 125
B. Ortho Iodination of phenols: This procedure allows for the incorporation of I at
the ortho position of a phenol as reported by Collier, T. L. and co-workers in J. Labelled
Compd. Radiopharm., 1999, 42, S264-S266.
C. Aryl and heteroaryl bromide exchange with I: This method is generally a two step
process. The first step is the conversion of the aryl or heteroaryl bromide to the corresponding
tri-alkyltin intermediate using for example, a Pd catalyzed reaction [i.e. Pd(Ph P) ] or through an
aryl or heteroaryl lithium, in the presence of a tri-alkyltinhalide or hexaalkylditin [e.g.,
(CH ) SnSn(CH ) ]. A representative procedure was reported by Le Bas, M.-D. and co-workers
3 3 3 3
in J. Labelled Compd. Radiopharm. 2001, 44, S280-S282.
A radiolabeled cannabinoid receptor compound can be used in a screening assay to
identify/evaluate compounds. In general terms, a newly synthesized or identified compound
(i.e., test compound) can be evaluated for its ability to reduce binding of the “radio-labeled
Compound 1” to a cannabinoid receptor. Accordingly, the ability of a test compound to compete
with the “radio-labeled Compound 1” for the binding to a cannabinoid receptor directly
correlates to its binding affinity.
Certain labeled compounds of the present invention bind to certain cannabinoid
receptors. In one embodiment the labeled compound has an IC less than about 500 µM, in
another embodiment the labeled compound has an IC less than about 100 µM, in yet another
embodiment the labeled compound has an IC less than about 10 µM, in yet another
embodiment the labeled compound has an IC less than about 1 µM and in still yet another
embodiment the labeled inhibitor has an IC less than about 0.1 µM.
Other uses of the disclosed receptors and methods will become apparent to those skilled
in the art based upon, inter alia, a review of this disclosure.
As will be recognized, the steps of the methods of the present invention need not be
performed any particular number of times or in any particular sequence. Additional objects,
advantages and novel features of this invention will become apparent to those skilled in the art
upon examination of the following examples thereof, which are illustrative and not limiting.
EXAMPLES
Example 1: Preparation of (1aS,5aS)(4-Oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-
diaza-cyclopropa[a]pentalenecarboxylic Acid ((S)Hydroxymethyl-2,2-dimethyl-
propyl)-amide (Compound 1).
Step A: Preparation of (1S,5R)-bicyclo[3.1.0]hexanone.
A 2.5 M hexane solution of n-BuLi (489 mL, 1223 mmol) was added dropwise to a
stirred solution of (S)(butenyl)oxirane (100 g, 1019 mmol) and 2,2,6,6-
tetramethylpiperidine (86 mL, 509 mmol) in MTBE (1000 mL) cooled in a dry ice/acetone bath,
at a rate to maintain the internal temperature at -12 to -5 °C (time of addition = 1 h). After
addition was complete, the reaction was stirred another hour at -5 to 0 °C.
While still at 0 °C, 3 M aqueous HCl (545 mL) was added (dropwise at first) with
stirring (internal temperature rose to 3 °C). The layers were separated and the organic layer
washed with another 200 mL 3 M HCl. The combined aqueous washings were extracted with
MTBE (2 x 500 mL). The combined organic layers were washed with brine (3 x 300 mL) then
concentrated (at 350 mbar and 29 °C water bath) to ca 1000 mL of pale yellow solution. This
solution was carried on without further purification.
To 407 mL water was added dibasic potassium phosphate (216 g, 1240 mmol),
monobasic potassium phosphate (12.8 g, 94 mmol), and potassium bromide (18.19 g, 153
mmol). pH paper indicated a pH of ~9. This aqueous solution was added to the MTBE solution
of (1S,2S,5R)-bicyclo[3.1.0]hexanol in a 5 L 3-neck round bottom flask equipped with an
overhead stirrer. The mixture was cooled to -20 °C in a dry-ice/isopropanol bath. TEMPO (4.30
g, 27.5 mmol) was added. The temperature was allowed to warm to 0 °C and aqueous 10-13%
sodium hypochlorite (1059 mL, 1630 mmol) was added dropwise while maintaining the internal
temperature between -10 and 0 °C (time of addition = 70 min). Stirring was continued at 0 °C
for another hour. 50 g sodium sulfite was added to quench excess sodium hypochlorite
(temperature rose to 12 °C). The layers were separated and the aqueous layer was extracted
twice more with MTBE (500 mL then 250 mL). The combined organic layers (total volume ca
1600 mL) were dried (MgSO ) then filtered. The solution was concentrated to ca 300 mL at 300
mbar and 35 °C water bath. The product was distilled--first with house vacuum and a 50 °C
water bath which distilled off most of the remaining MTBE. The vacuum pump was connected
giving a vacuum of ~2 torr and the product distilled (2 torr/36 °C) to give the title compound
(65.8 g) as a light orange oil (note: receiving flask was cooled in dry ice/acetone bath). H NMR
(400 MHz, CDCl ) 0.93 (td, J = 4.6, 3.3 Hz, 1H), 1.20 (td, J = 8.0, 4.8 Hz, 1H), 1.74-1.79 (m,
1H), 1.98-2.19 (m, 5H).
Step B: Preparation of 2-Hydrazinylpyrazine.
The reaction was run under nitrogen atmosphere. 2-chloropyrazine (96 mL, 1073 mmol)
was added dropwise to 35 wt% aqueous hydrazine (544 mL, 6009 mmol) at 65 °C over 1 h.
After the addition, stirring was continued at 63-67 °C for 16 h then let stand at room temperature
for two days. The mixture was filtered to remove a small amount of precipitate, then extracted
with 10% iPrOH/dichloromethane (5 x 250 mL). The combined organic extracts were dried
(MgSO ), filtered, then concentrated under reduced pressure. The resulting solid was triturated
with isopropyl acetate (600 mL). The solid was collected by filtration, rinsed with isopropyl
acetate and dried under vacuum to give 2-hydrazinylpyrazine (60 g, 51%) as a pale yellow solid.
LCMS m/z = 111.2 [M+H] . H NMR (400 MHz, DMSO-d ) 4.21 (s, 2H), 7.70 (d, J = 2.8 Hz,
1H), 7.89 (s, 1H), 7.93 (dd, J = 2.8, 1.5 Hz, 1H), 8.10 (d, J = 1.5 Hz, 1H).
Step C: Preparation of (1aS,5aS)(Pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-
diaza-cyclopropa[a]pentalenecarboxylic Acid Ethyl Ester.
To a solution of (1S,5R)-bicyclo[3.1.0]hexanone (52.9 g, 539 mmol) and diethyl
oxalate (0.073 L, 539 mmol) in absolute ethanol (0.9 L) (not denatured with methanol) was
added a 1.0 M THF solution of potassium tert-butoxide (0.539 L, 539 mmol) over 15 min
(maintaining the temperature below 43 °C). The resulting yellow solution was stirred at 40 °C
for 3.5 h (a precipitate appeared within 10 min and the reaction eventually became a thick
suspension). 2-hydrazinylpyrazine (59.4 g, 539 mmol) was added followed by a 6.0 M aqueous
solution of hydrogen chloride (0.270 L, 1618 mmol). The reaction was stirred at 50 °C for 1.5 h.
The mixture was poured into ice-water (5 L). A precipitate appeared immediately. After
standing for 30 minutes in an ice bath, the solid was collected by filtration, rinsed with water (5
x 1 L), then dried, affording the title product (106 g, 73%) as an off-white solid. LCMS m/z =
271.2 (M+H ). H NMR (400 MHz, CDCl ) 0.47 (td, J = 4.7, 3.3 Hz, 1H), 1.27 (td, J = 8.0,
4.9 Hz, 1H), 1.41 (t, J = 7.1 Hz, 3H), 2.26-2.32 (m, 1H), 2.77-2.82 (m, 1H), 2.88 (dd, J = 16.7,
1.4 Hz, 1H), 2.99 (dd, J = 16.6, 6.4 Hz, 1H), 4.40 (q, J = 7.1 Hz, 2H), 8.41 (dd, J = 2.5, 1.5 Hz,
1H), 8.52 (d, J = 2.5 Hz, 1H), 9.40 (d, J = 1.5 Hz, 1H).
Step D: Preparation of (1aS,5aS)(Pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-
diaza-cyclopropa[a]pentalenecarboxylic Acid.
To a suspension of (1aS,5aS)(pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-
cyclopropa[a]pentalenecarboxylic acid ethyl ester (106 g, 392 mmol) in MeOH (300 mL) and
THF (300 mL) was added a 2.0 M aqueous solution of NaOH (235 mL, 471 mmol). The mixture
was stirred at 23 °C for 20 h. The organic solvents were removed by distillation. The remaining
aqueous solution was diluted with water to ca 1.5 L then acidified to pH ~2 with 6 M HCl (ca 95
mL). The resulting fine precipitate was collected by filtration, rinsed with water, then dried, to
give the title compound (95 g, 100%) as a white solid. LCMS m/z = 243.1 (M+H ). H NMR
(400 MHz, DMSO-d6) 0.43 (td, J = 4.6, 3.2 Hz, 1H), 1.26 (td, J = 8.0, 4.4 Hz, 1H), 2.27-2.33
(m, 1H), 2.71-2.75 (m, 1H), 2.76 (d, J = 16.8 Hz, 1H), 2.89 (dd, J = 16.4, 6.4 Hz, 1H), 8.61 (dd,
J = 2.7, 1.5 Hz, 1H), 8.67 (d, J = 2.5 Hz, 1H), 9.17 (d, J = 1.5 Hz, 1H), 13.02 (s, 1H).
Two separate methods were used to prepare Compound 1, one method oxidized the
pyrazinyl ring nitrogen as the last reaction step while the second method oxidized the pyrazinyl
ring nitrogen of the carboxylic acid intermediate (i.e., title compound in of Step D) prior to the
coupling with (S)amino-3,3-dimethylbutanol. Steps E and F are shown below.
METHOD 1
Step E: Preparation of (1aS,5aS)Pyrazinyl-1a,2,5,5a-tetrahydro-1H-2,3-
diaza-cyclopropa[a]pentalenecarboxylic acid ((S)hydroxymethyl-2,2-dimethyl-
propyl)-amide.
To a solution of (1aS,5aS)(pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-
cyclopropa[a]pentalenecarboxylic acid (1.4 g, 5.78 mmol) and triethylamine (1.611 mL,
11.56 mmol) in DMF (15 mL) was added HATU (2.242 g, 5.90 mmol). The reaction was stirred
at 23 °C for 5 min, then was added (S)amino-3,3-dimethylbutanol (0.711 g, 6.07 mmol).
The reaction was stirred at 23 °C for 15 min then concentrated. The residue was purified by
silica gel flash chromatography (35 to 100% EtOAc/hexanes) to give the title product (1.97 g,
100%) as a white solid. LCMS m/z = 342.2 [M+H] . H NMR (400 MHz, CDCl ) 0.48 (td, J =
4.6, 3.4 Hz, 1H), 1.05 (s, 9H), 1.24 (td, J = 8.0, 4.7 Hz, 1H), 2.26-2.32 (m, 1H), 2.74-2.78 (m,
1H), 2.94 (d, J = 16.8 Hz, 1H), 3.01 (dd, J = 16.7, 6.1 Hz, 1H), 3.67-3.72 (m, 1H), 3.93-3.98 (m,
2H), 7.08 (d, J = 8.5 Hz, 1H), 8.42 (dd, J = 1.4, 0.9 Hz, 1H), 8.51 (d, J = 2.7 Hz, 1H), 9.26 (d, J
= 1.1 Hz, 1H).
Step F: Preparation of (1aS,5aS)(4-Oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-
2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S)hydroxymethyl-2,2-dimethyl-
propyl)-amide (Compound 1).
To a solution of (1aS,5aS)pyrazinyl-1a,2,5,5a-tetrahydro-1H-2,3-diaza-
cyclopropa[a]pentalenecarboxylic acid ((S)hydroxymethyl-2,2-dimethyl-propyl)-amide
(900 mg, 2.64 mmol) in chloroform (10 mL) was added 3-chlorobenzoperoxoic acid (1772 mg,
7.91 mmol). The reaction was stirred at 23 °C for 3 h. Additional MCPBA (1.2 g) was added
and stirring was continued at room temperature for 18 h. The mixture was purified by silica gel
column chromatography to give the title compound (550 mg) as a white solid. LCMS m/z =
358.3 [M+H] ; H NMR (400 MHz, CDCl ) δ ppm 0.49 (td, J = 4.6, 3.3 Hz, 1H), 1.03 (s, 9H),
1.27 (td, J = 8.0, 4.9 Hz, 1H), 2.08 (bs, 1H), 2.27-2.33 (m, 1H), 2.71-2.76 (m, 1H), 2.93 (d, J =
16.8 Hz, 1H), 3.00 (dd, J = 16.7, 6.1 Hz, 1H), 3.65-3.71 (m, 1H), 3.92-3.97 (m, 2H), 6.97 (d, J =
8.5 Hz, 1H), 7.99 (dd, J = 4.0, 1.4 Hz, 1H), 8.28 (d, J = 4.2 Hz, 1H), 8.78 (dd, J = 1.4, 0.8 Hz,
1H).
A sample was recrystallized from CH Cl /hexane to give a crystalline solvate. A
thermogravimetric analysis (TGA) thermogram for this solvate showed a loss of ~5% weight
occurring with a melting endotherm at 164°C.
A non-solvated form of Compound 1 was slurried in CH Cl and stirred at ~28°C
overnight. The suspension was filtered using a centrifuge filter and air dried prior to powder X-
ray diffraction (PXRD) pattern analysis. The PXRD pattern showed that the material following
the CH Cl slurry was indistinguishable from the original solvate form that resulted from
recrystallization with CH Cl /hexane. The differential scanning calorimetry (DSC) thermogram
and thermogravimetric analysis (TGA) thermogram for the crystalline CH Cl solvate obtained
from recrystallization using CH Cl /hexane is shown in Figure 1; and the PXRD pattern for
each of the crystalline CH Cl solvates obtained from the two different methods (i.e.,
recrystallization using CH Cl /hexane; and non-solvated Compound 1 slurried in CH Cl ) is
2 2 2 2
shown as an overlay in Figure 2.
METHOD 2
Step E: Preparation of (1aS,5aS)(Pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-
diaza-cyclopropa[a]pentalenecarboxylic Acid N-oxide.
To a suspension of (1aS,5aS)(pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-
cyclopropa[a]pentalenecarboxylic acid (68.8 g, 284 mmol) in formic acid (688 mL) was
added a 50 wt% aq solution of hydrogen peroxide (82 mL, 1420 mmol) at room temperature.
The mixture was heated to 64 °C. The reaction was stirred at 58 to 64 °C for 3 h. Another 8 mL
50% H O was added and stirring was continued another hour at 60 °C. The mixture was let cool
to room temperature and diluted with 1 L water. After storing in an ice bath for 1 h, the
precipitate was collected by filtration, rinsed with water and dried under vacuum to give the title
compound (56.7 g) as a pale yellow solid which contains 2 % starting material by H NMR. The
material was re-subjected to reaction conditions aforementioned to give the title compound (45
g). LCMS m/z = 259.2 [M+H] ; H NMR (400 MHz, DMSO-d ) 0.42 (td, J = 4.4, 3.3 Hz,
1H), 1.27 (td, J = 7.8, 4.7 Hz, 1H), 2.27-2.33 (m, 1H), 2.68-2.73 (m, 1H), 2.75 (dd, J = 16.9, 1.5
Hz, 1H), 2.88 (dd, J = 16.4, 6.4 Hz, 1H), 8.33 (dd, J = 4.2, 1.5 Hz, 1H), 8.50 (dd, J = 4.2, 0.6
Hz, 1H), 8.54 (dd, J = 1.5, 0.6 Hz, 1H), 13.08 (s, 1H).
Step F: Preparation of (1aS,5aS)(4-Oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-
2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S)hydroxymethyl-2,2-dimethyl-
propyl)-amide(Compound 1).
To a suspension of (1aS,5aS)(pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-
cyclopropa[a]pentalenecarboxylic acid N-oxide (46.82 g, 181 mmol), (S)amino-3,3-
dimethylbutanol (23.37 g, 199 mmol) and triethylamine (76 mL, 544 mmol) in DMF (400
mL) was added HATU (76 g, 199 mmol). The reaction was stirred at 23 °C for 60 min and
concentrated. 0.5 M HCl (500 mL) was added. The mixture was extracted with dichloromethane
(3 x 400 mL). The combined organic extracts were washed with saturated NaHCO (2 x 250
mL), dried (MgSO ), filtered, then concentrated to ~250 mL. To the resulting slurry was added
500 mL of hexanes. The mixture was let stand at room temperature for several hours and the
solid was collected by filtration to give the title compound (55 g) as an off-white solid. This
material was recrystallized from DCM/hexanes to give the title compound (43.5 g) as a white
solid (after drying in vacuum oven at ~65 °C for 10 days). LCMS m/z = 358.3 [M+H] ; H NMR
(400 MHz, CDCl ) δ ppm 0.49 (td, J = 4.6, 3.3 Hz, 1H), 1.03 (s, 9H), 1.27 (td, J = 8.0, 4.9 Hz,
1H), 2.08 (bs, 1H), 2.27-2.33 (m, 1H), 2.71-2.76 (m, 1H), 2.93 (d, J = 16.8 Hz, 1H), 3.00 (dd, J
= 16.7, 6.1 Hz, 1H), 3.65-3.71 (m, 1H), 3.92-3.97 (m, 2H), 6.97 (d, J = 8.5 Hz, 1H), 7.99 (dd, J
= 4.0, 1.4 Hz, 1H), 8.28 (d, J = 4.2 Hz, 1H), 8.78 (dd, J = 1.4, 0.8 Hz, 1H).
Example 2: Preparation of (1aS,5aS)(4-Oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-
diaza-cyclopropa[a]pentalenecarboxylic Acid ((S)Hydroxymethyl-2,2-dimethyl-
propyl)-amide (Compound 1, DCM Solvate).
The DCM hemi-solvate (10.6% by weight) was obtained by slow crystallization from
CH Cl and hexanes and the crystal structure of this material was solved, see Figure 3. Further
attempts to isolate the hemi-DCM solvate by forming a slurry of Compound 1 with DCM
resulted in substantially the same DCM Solvates as disclosed in International Publication
Number WO2011/025541, an overlay of the PXRDs of the previous disclosed DCM solvate is
shown in Figure 2.
Example 3: Preparation of (1aS,5aS)(4-Oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-
diaza-cyclopropa[a]pentalenecarboxylic Acid ((S)Hydroxymethyl-2,2-dimethyl-
propyl)-amide (Compound 1, Anhydrous Form).
The anhydrous form of Compound 1 was prepared by recrystallization in DCM and
hexanes. The PXRD pattern was characterized, see Figure 4. This material melts at ~162°C and
is a non-solvated form based on TGA Figure 5.
It should be noted that the use of mixtures of DCM/hexanes as recrystallizing solvents
have been observed at different times to provide different crystal forms.
Example 4: Preparation of (1aS,5aS)(4-Oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-
diaza-cyclopropa[a]pentalenecarboxylic Acid ((S)Hydroxymethyl-2,2-dimethyl-
propyl)-amide (Compound 1, Anhydrous Form).
Method 1
To a 4L reactor equipped with an overhead stirrer, chiller/heater, and a dropping funnel
was added (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-
cyclopropa[a]pentalenecarboxylic acid ((S)hydroxymethyl-2,2-dimethyl-propyl)-amide
(Compound 1, 145 g, 406 mmol), acetonitrile (205 mL, 3925 mmol), and water (290 mL). The
mixture was heated to 60°C and then stirred for 60 min. To the resulting reaction was added an
additional amount of water (2900 mL), cooled to 0°C, and allowed to stir for 4 h. The mixture
was filtered, the solids washed with water and dried under vacuum at 50°C to provide
Compound 1 as the anhydrous form, the material was characterized by PXRD (Figure 6), and
DSC/TGA (Figure 7).
Method 2
The anhydrous form of (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-
diaza-cyclopropa[a]pentalenecarboxylic acid ((S)hydroxymethyl-2,2-dimethyl-propyl)-
amide (Compound 1) was prepared in a similar manner as described in Method 1 except that
after isolating crystalline (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-
cyclopropa[a]pentalenecarboxylic acid ((S)hydroxymethyl-2,2-dimethyl-propyl)-amide
from the acetonitrile/water crystallizing mixture the material was dried under vacumm at 60°C ±
°C to provide Compound 1 as the anhydrous form. The anhydrous form prepared according to
Method 2 was characterized by PXRD, DSC, and TGA and was found to be substantially
similar to the material prepared according to Method 1.
Example 5: Preparation of (1aS,5aS)(4-Oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-
diaza-cyclopropa[a]pentalenecarboxylic Acid ((S)Hydroxymethyl-2,2-dimethyl-
propyl)-amide (Compound 1, Acetone Solvate).
The Acetone Solvate of Compound 1 was prepared from a slurry of Compound 1 in
acetone. The PXRD pattern was characterized, see Figure 8. This material showed a loss of
weight by TGA of about 5.5%, a desolvation endotherm began at about 100°C and subsequent
melting onset endotherm temperate at about 163°C, see Figure 9. The acetone solvate was
reproduced from a different lot of anhydrous Compound 1, the PXRD is substantially identical
to that seen in Figure 8 but with a different loss of acetone as shown by TGA, and thus the
stoichiometry of this solvate can be characterized as a variable or non-stoichiometric acetone
solvate of Compound 1.
Example 6: Preparation of (1aS,5aS)(4-Oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-
diaza-cyclopropa[a]pentalenecarboxylic Acid ((S)Hydroxymethyl-2,2-dimethyl-
propyl)-amide (Compound 1, Non-Selective Solvates).
The solvate of Compound 1 was prepared from a slurry of Compound 1 in ethyl acetate.
The PXRD pattern was characterized, see Figure 10. The substantially identical PXRD pattern
was twice generated from material prepared by slurring Compound 1 in THF, see Figure 11.
Further, the substantially identical PXRD pattern was twice generated from material prepared by
slurring Compound 1 in methyl ethyl ketone (MEK), see Figure 12. Further, the non-selective
solvate of Compound 1 prepared using ethyl acetate showed a weight loss of weight of about
4.8% up to about 150 °C with an extrapolated onset temperature of 160.8 °C; see TGA and DSC
(Figure 13). The non-selective solvate of Compound 1 prepared using THF showed a weight
loss of about 6.8% up to about 150 °C with an extrapolated onset temperature of 161.0 °C; see
TGA and DSC (Figure 14). The non-selective solvate of Compound 1 prepared using MEK
showed a weight loss of about 4.5% up to about 150 °C with an extrapolated onset temperature
of 160.5 °C; see TGA and DSC (Figure 15).
The non-selective solvates of Compound 1, independent of the solvent used to prepare
the solvate, showed substantially the same PXRD as seen in Figures 10, 11, and 12 and after
desolvation of the solvate each melts with an extrapolated onset temperature of about 161 °C,
see Figures 13, 14, and 15. These solvates appear to be a non-stoichiometric, non-selective
solvate crystalline forms of Compound 1 based on TGA.
Example 7: Preparation of (1aS,5aS)(4-Oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-
diaza-cyclopropa[a]pentalenecarboxylic Acid ((S)Hydroxymethyl-2,2-dimethyl-
propyl)-amide (Compound 1, Ethyl Acetate Solvate).
A ethyl acetate solvate of Compound 1 was prepared by recrystallization from ethyl
acetate and heptane. (1aS,5aS)(4-Oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-
cyclopropa[a]pentalenecarboxylic acid ((S)hydroxymethyl-2,2-dimethyl-propyl)-amide
(Compound 1, 430-580 mmol) was dissolved in ethyl acetate (450 mL) at 45°C. The mixture
was then cooled to 25°C and 100 mL of heptane was added to the reactor. The mixture was
allowed to stir for 20 min at 22°C. Heptane (2250 mL) was then charged and heated to 55°C.
The mixture was allowed to stir overnight at 25°C. The reaction was then cooled to 20°C and
then filtered and washed with 500 mL heptane. The filter cake was dried under vacuum at 45°C.
The PXRD pattern was characterized, see Figure 16. The ethyl acetate solvate showed a broad
desolvation endotherm from about 30-110°C, corresponding to a 1% weight loss on the TGA,
see Figure 17. There is a second, larger desolvation/melting endotherm at about 115-135°C,
corresponding to a TGA weight loss of about 4%. The combined weight loss is consistent with
the NMR, which showed approximately 17 mole percent of ethyl acetate, which is equivalent to
about 4.7% by weight. This solvate can contain a trace amount of heptane.
Example 8: PathHunter β-Arrestin Assay
A: CB Assay
Compound 1 was screened for agonist activity against the human CB receptor using the
DiscoveRx PathHunter β-arrestin assay which measures the β-arrestin binding to the CB
receptor upon its activation. CB was cloned into the pCMV-PK vector (DiscoveRx, Fremont,
CA; catalog # 93-0167) and transfected into the CHO-K1 EA-Arrestin parental cell line
(DiscoveRx, Fremont, CA; catalog # 93-0164). CHO-K1 positive clones stably expressing the
CB -ProLink fusion protein were identified by their responses to the CB agonist CP55,940.
Clone # 61 was chosen for its big agonist window and homogenous expression as detected by
anti-HA flow cytometry
Principle of the assay: The PathHunter β-arrestin assay measures the interaction of β-
arrestin with activated GPCRs using Enzyme Fragment Complementation (Yan et al., J. Biomol.
Screen. 7: 451-459, 2002). A small, 42 amino acid β-galactosidase fragment, Prolink, is fused to
the c-terminus of a GPCR, and β-arrestin is fused to the larger β-galactosidase fragment, EA
(Enzyme Acceptor). Binding of β-arrestin to the activated GPCR causes the complementation of
the two enzyme fragments, forming an active β-galactosidase enzyme which can be measured
using the chemiluminiescent PathHunter Flash Detection Kit (DiscoveRx, Fremont, CA: catalog
# 93-0001).
The assay: The stable CHO-K1 cells expressing CB -Prolink fusion protein were plated
over night in 384-well plates (Optiplate 384-Plus, PerkinElmer, Fremont CA; catalog #
6007299) at 5000 cells/5 µL/well in the Opti-MEM medium (Invitrogen, Carlsbad, CA; catalog
# 31985088) with 1% FBS. 5uL of test compound diluted in Opti-MEM supplemented with 1%
BSA was transferred to each well of the Optiplate. The plates were then incubated at 37 °C/5%
CO for two hours. 12 µL of substrate prepared from the PathHunter Flash Detection Kit
(DiscoveRx, Fremont, CA: catalog # 93-0001) was transferred to each well of the Optiplate. The
plate was then incubated in the dark at room temperature for 2 h, after which the assay plate was
read.
Assay readout: β-Arrestin assay readout was accomplished using a PHERAstar (BMG
Labtech Inc., Durham, NC) or an EnVision™ (PerkinElmer, Fremont CA) microplate reader.
B: CB Assay
Compound 1 was screened for agonist activity against the human CB receptor using the
DiscoveRx PathHunter β-arrestin assay which measures the β-arrestin binding to the CB
receptor upon its activation. CB was cloned into the pCMV-PK vector (DiscoveRx, Fremont,
CA; catalog # 93-0167) and transfected into the CHO-K1 EA-Arrestin parental cell line
(DiscoveRx, Fremont, CA; catalog # 93-0164). CHO-K1 positive clones stably expressing the
CB -ProLink fusion protein were identified by their responses to the CB agonist CP55,940.
Clone # 3 was chosen for its big agonist window and homogenous expression as detected by
anti-HA flow cytometry
Principle of the assay: The PathHunter β-arrestin assay measures the interaction of β-
arrestin with activated GPCRs using Enzyme Fragment Complementation (Yan et al., J. Biomol.
Screen. 7: 451-459, 2002). A small, 42 amino acid β-galactosidase fragment, Prolink, is fused to
the c-terminus of a GPCR, and β-arrestin is fused to the larger β-galactosidase fragment, EA
(Enzyme Acceptor). Binding of β-arrestin to the activated GPCR causes the complementation of
the two enzyme fragments, forming an active β-galactosidase enzyme which can be measured
using the chemiluminiescent PathHunter Flash Detection Kit (DiscoveRx, Fremont, CA: catalog
# 93-0001).
The assay: The stable CHO-K1 cells expressing CB -Prolink fusion protein were plated
over night in 384-well plates (Optiplate 384-Plus, PerkinElmer, Fremont CA; catalog #
6007299) at 5000 cells/5 µL/well in the Opti-MEM medium (Invitrogen, Carlsbad, CA; catalog
# 31985088) with 1% FBS. 5uL of test compound diluted in Opti-MEM supplemented with 1%
BSA was transferred to each well of the Optiplate. The plates were then incubated at 37 °C/5%
CO for two h. 12 µL of substrate prepared from the PathHunter Flash Detection Kit
(DiscoveRx, Fremont, CA: catalog # 93-0001) was transferred to each well of the Optiplate. The
plate was then incubated in the dark at room temperature for 2 h, after which the assay plate was
read.
Assay readout: β-Arrestin assay readout was accomplished using a PHERAstar (BMG
LABTECH Inc., Durham, NC) or EnVision™ (PerkinElmer, Fremont CA) microplate reader.
The EC value for hCB was observed to be substantially inactive and the EC value
50 1 50
observed for hCB for Compound 1 is shown in the following Table. Compound 1 is a selective
agonist for CB .
EC hCB (nM)
50 2
Compound 1 5.4
Example 9: Effect of Compound 1 on Osteoarthritis pain.
Injection of monosodium iodoacetate (MIA) into a joint (Kalbhen D. A., J. Rheumatol.,
1987, May;14 Spec No:130-1; Combe, R., et. al., Neuroscience Letters, 2004, 370, 236–240)
inhibits the activity of glyceraldehydephosphate dehydrogenase in chondrocytes, resulting in
disruption of glycolysis and eventually in cell death. The progressive loss of chondrocytes
results in histological and morphological changes of the articular cartilage, closely resembling
those seen in osteoarthritis patients.
The osteoarthritis was induced in 200 g male Sprague Dawley rats. After brief
anaesthesia by isoflurane rats received a single intra-articular injection of MIA (2 mg) (Sigma
Aldrich, Saint Louis, MO, USA; Cat # I9148) dissolved in 0.9% sterile saline in a 50 µL volume
administered through the patella ligament into the joint space of the left knee with a 30G needle.
Following the injection, animals were allowed to recover from anaesthesia before being returned
to the main housing vivarium.
Typically during disease progression, there was an inflammation period of 0-7 days
post-intra-articular injection followed by progressive degeneration of the cartilage and
subchondral bone from days 14-55. Efficacy studies with a compound of the present invention
for pain development took place from day 14 onwards and were performed twice a week with at
least 3 days' wash-out in between each assay. Three different assays were used to measure pain.
Tactile allodynia was measured via von Frey assay, hind limb paw weight distribution was
monitored using an incapacitence tester (Columbus Instruments, Columbus, OH, USA) and hind
limb grip strength was measured using a grip strength meter (Columbus Instruments, Columbus,
OH, USA). Briefly, the von Frey assay was performed using the standard up down method with
von-Frey filaments. Hind paw weight distribution was determined by placing rats in a chamber
so that each hind paw rests on a separate force plate of the incapacitence tester. The force
exerted by each hind limb (measured in grams) is averaged over a 3 second period. Three
measurements were taken for each rat, and the change in hind paw weight distribution
calculated. Peak hind limb grip force was conducted by recoding the maximum compressive
force exerted on the hind limb mesh gauge set on the grip strength meter. During the testing,
each rat was restrained and the paw of the injected knee was allowed to grip the mesh. The
animal was then pulled in an upward motion until their grip was broken. Each rat is tested 3
times, with the contralateral paw used as a control.
Animals were base-lined prior to treatment of the test compound. The MIA treated
groups of rats (6 per group) were then dosed with either vehicle (0.5% methylcellulose,
orally), Compound 1 (at 3 mg/kg, 10 mg/kg, and 30 mg/kg, orally). Dosing volume was 500
µL. One hour after dosing, von Frey assay, hind limb weight distribution and/or hind limb
grip analysis was performed to measure the efficacy of the test compound. Increase in paw
withdrawal threshold (PWT) by Compound 1 in comparison with vehicle shown in Figure 18
was indicative of the test compound exhibiting therapeutic efficacy in the MIA model of
osteoarthritis.
Example 10: Powder X-ray Diffraction.
Powder X-ray Diffraction (PXRD) data were collected on an X'Pert PRO MPD powder
diffractometer (PANalytical, Inc.) with a Cu source set at 45 kV and 40 mA, Cu(Kα) radiation
and an X'Celerator detector. Samples were added to the sample holder and smoothed flat with a
spatula and weigh paper. With the samples spinning, X-ray diffractograms were obtained by a
12-min scan over the 2-theta range 5-40 °2 . Diffraction data were viewed and analyzed with
the X'Pert Data Viewer Software, version 1.0a and X’Pert HighScore Software, version 1.0b.
Example 11: Differential Scanning Calorimetry.
Differential scanning calorimetry (DSC) studies were conducted using a TA
Instruments, Q2000 at a heating rate 10°C/min. The instruments were calibrated for temperature
and energy using the melting point and enthalpy of fusion of an indium standard. Thermal
events (desolvation, melting, etc.) were evaluated using Universal Analysis 2000 software,
version 4.1D, Build 4.1.0.16.
Example 12: Thermal Gravimetric Analysis.
Thermogravimetric analyses (TGA) were conducted using a TA Instruments TGA Q500
or Q5000 at a heating rate 10 °C/min. The instruments were calibrated using a standard weight
for the balance, and Alumel and Nickel standards for the furnace (Curie point measurements).
Thermal events such as weight-loss are calculated using the Universal Analysis 2000 software,
version 4.1D, Build 4.1.0.16.
Example 13: Dynamic Moisture-Sorption Analysis.
A dynamic moisture-sorption (DMS) study was conducted using a dynamic moisture-
sorption analyzer, VTI Corporation, SGA-100. The instrument was calibrated using polyvinyl
pyrrolidone (PVP) and NaCl. Samples were prepared for DMS analysis by placing 5 mg to 20
mg of a sample in a tared sample holder. The sample was placed on the hang-down wire of the
VTI balance. A drying step was run, typically at 40 °C and 0.5-1% RH for 1 h. The isotherm
temperature is 25 °C. Defined % RH holds typically ranged from 10% RH to 90% RH, with
intervals of 10 to 20% RH. A% weight change smaller than 0.010% over 10 min, or up to 2 h,
whichever occurred first, was required before continuing to the next % RH hold. The water
content of the sample equilibrated as described above was determined at each % RH hold.
The DMS profile (adsorption/desorption isotherm) for the anhydrous crystalline form of
Compound 1 is shown in Figure 7A. The corresponding data in tabular form is provided below:
Elapsed
Weight Weight Sample Sample
Time
(mg) (% Change) Temperature RH (%)
(min)
46.6 9.6782 0 25.46 1.1
71.4 9.6928 0.151 25.32 29.94
91.1 9.7055 0.282 25.31 49.86
111.2 9.7248 0.482 25.3 69.77
129.1 9.7344 0.581 25.29 . 79.70
160.1 9.7519 0.762 25.3 89.72
180.1 9.7291 0.526 25.30 70.11
200.1 9.7134 0.364 25.3 50.07
218.6 9.6957 0.181 25.29 29.99
234.4 9.6859 0.080 25.29 10.06
Those skilled in the art will recognize that various modifications, additions,
substitutions, and variations to the illustrative examples set forth herein can be made without
departing from the spirit of the invention and are, therefore, considered within the scope of the
invention.
Claims (43)
1. A process for preparing an anhydrous crystalline form of (1aS,5aS)(4-oxy-pyrazin yl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S) hydroxymethyl-2,2-dimethyl-propyl)-amide comprising the steps of: 1) crystallizing (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H- 10 2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S)hydroxymethyl-2,2- dimethyl-propyl)-amide from a crystallizing mixture to obtain a crystalline form of (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza- cyclopropa[a]pentalenecarboxylic acid ((S)hydroxymethyl-2,2-dimethyl-propyl)- amide in said crystallizing mixture, wherein said crystallizing mixture comprises 15 acetonitrile and water; and 2) isolating said crystalline form of (1aS,5aS)(4-oxy-pyrazinyl)- 1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S) hydroxymethyl-2,2-dimethyl-propyl)-amide from said crystallizing mixture to obtain said anhydrous crystalline form of (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a- 20 tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S) hydroxymethyl-2,2-dimethyl-propyl)-amide.
2. The process according to claim 1, wherein said crystallizing is conducted at a temperature of about -5 °C to about 5 °C.
3. The process according to claim 1 or 2, wherein said crystallizing mixture is prepared by the steps of: 1) dissolving (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H- 2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S)hydroxymethyl-2,2- 30 dimethyl-propyl)-amide in acetonitrile and a first amount of water to form a first mixture; and 2) adding a second amount of water to said first mixture to obtain said crystallizing mixture. 35
4. The process according to claim 3, wherein said dissolving is conducted at a temperature of about 58 °C to about 62 °C.
5. The process according to claim 3 or 4, wherein the molar ratio present in said first mixture between (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza- cyclopropa[a]pentalenecarboxylic acid ((S)hydroxymethyl-2,2-dimethyl-propyl)- amide, acetonitrile, and first amount water is about 1.0:9.2:37.0 to about 1.0:10.2:41.7.
6. The process according to any one of claims 3 to 5, wherein said adding of said second amount of water to said first mixture is conducted at a rate that the temperature of the mixture of said second amount of water together with said first mixture is at about 25 °C to about 80 °C.
7. The process according to any one of claims 3 to 6, wherein the molar ratio present in said crystallizing mixture between (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a- tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S) hydroxymethyl-2,2-dimethyl-propyl)-amide, acetonitrile, and water in said crystallizing 15 mixture is about 1.0:9.2:414.7 to about 1.0:10.2:458.3.
8. The process according to any one of claims 3 to 7, wherein (1aS,5aS)(4-oxy-pyrazin- 2-yl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S)- 1-hydroxymethyl-2,2-dimethyl-propyl)-amide prior to said dissolving step is selected 20 from the group consisting of: 1) a dichloromethane solvate of (1aS,5aS)(4-oxy-pyrazinyl)- 1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S) hydroxymethyl-2,2-dimethyl-propyl)-amide; 2) an acetone solvate of (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a- 25 tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S) hydroxymethyl-2,2-dimethyl-propyl)-amide; 3) a non-selective solvate of (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a- tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S) hydroxymethyl-2,2-dimethyl-propyl)-amide; and 30 4) an ethyl acetate solvate of (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a- tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S) hydroxymethyl-2,2-dimethyl-propyl)-amide; and mixtures thereof. 35
9. The process according to any one of claims 1 to 8, wherein said isolating comprises filtering said crystalline form of (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro- 1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S)hydroxymethyl-2,2- dimethyl-propyl)-amide from said crystallizing mixture.
10. The process according to any one of claims 1 to 8, wherein said isolating comprises removing said crystalline form of (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a- tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S) 5 hydroxymethyl-2,2-dimethyl-propyl)-amide from said crystallizing mixture.
11. The process according to any one of claims 1 to 10, further comprises the step of drying said crystalline form of (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3- diaza-cyclopropa[a]pentalenecarboxylic acid ((S)hydroxymethyl-2,2-dimethyl- 10 propyl)-amide to obtain said anhydrous crystalline form of (1aS,5aS)(4-oxy-pyrazin- 2-yl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S)- 1-hydroxymethyl-2,2-dimethyl-propyl)-amide.
12. The process according to claim 11, wherein said drying is conducted at a temperature of 15 about 15 °C to about 80 °C.
13. The process according to claim 11, wherein said drying is conducted at a pressure of less than 760 mm Hg and a temperature of about 55 °C to about 65 °C. 20
14. The process according to any one of claims 1 to 13, wherein after said isolating, said anhydrous crystalline form of (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro- 1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S)hydroxymethyl-2,2- dimethyl-propyl)-amide has a chemical purity of about 98% or greater. 25
15. The process according to any one of claims 1 to 14, wherein after said isolating, said anhydrous crystalline form of (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro- 1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S)hydroxymethyl-2,2- dimethyl-propyl)-amide has an enantiomeric excess of about 98% or greater. 30
16. The process according to any one of claims 1 to 13, wherein after said isolating, said anhydrous crystalline form of (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro- 1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S)hydroxymethyl-2,2- dimethyl-propyl)-amide has a chemical purity of about 99% or greater and an enantiomeric excess of about 99% or greater.
17. A process for preparing a pharmaceutical composition comprising the steps of: 1) preparing an anhydrous crystalline form of (1aS,5aS)(4-oxy-pyrazin- 2-yl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S)- 1-hydroxymethyl-2,2-dimethyl-propyl)-amide according to any one of claims 1 to 16; 2) admixing said anhydrous crystalline form of (1aS,5aS)(4-oxy- pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic 5 acid ((S)hydroxymethyl-2,2-dimethyl-propyl)-amide with a phamaceutically acceptable carrier.
18. A process for preparing a dosage form comprising the steps of: 1) preparing an anhydrous crystalline form of (1aS,5aS)(4-oxy-pyrazin- 10 2-yl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S)- 1-hydroxymethyl-2,2-dimethyl-propyl)-amide according to any one of claims 1 to 16; 2) admixing said anhydrous crystalline form of (1aS,5aS)(4-oxy- pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic 15 acid ((S)hydroxymethyl-2,2-dimethyl-propyl)-amide with a phamaceutically acceptable carrier.
19. An anhydrous crystalline form of (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a- tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S) 20 hydroxymethyl-2,2-dimethyl-propyl)-amide.
20. The process according to any one of claims 1 to 18 or the anhydrous crystalline form according to claim 19, wherein said anyhydrous crystalline form has a powder X-ray diffraction pattern comprising peaks, in terms of 2 , at 8.5° ± 0.2°, and 10.7° ± 0.2°.
21. The process according to any one of claims 1 to 18 or the anhydrous crystalline form according to claim 19, wherein said anyhydrous crystalline form has a powder X-ray diffraction pattern comprising peaks, in terms of 2 , at 8.5° ± 0.2°, 10.7° ± 0.2°, and 16.9° ± 0.2°.
22. The process according to any one of claims 1 to 18 or the anhydrous crystalline form according to claim 19, wherein said anyhydrous crystalline form has a powder X-ray diffraction pattern comprising peaks, in terms of 2 , at 8.5° ± 0.2°, 10.7° ± 0.2°, 16.9° ± 0.2°, 25.4° ± 0.2°, and 11.1° ± 0.2°.
23. The process according to any one of claims 1 to 18 or the anhydrous crystalline form according to claim 19, wherein said anyhydrous crystalline form has a powder X-ray diffraction pattern comprising peaks, in terms of 2 , at 8.5° ± 0.2°, 10.7° ± 0.2°, 16.9° ± 0.2°, 25.4° ± 0.2°, 11.1° ± 0.2°, 9.8° ± 0.2°, and 17.4° ± 0.2°.
24. The process according to any one of claims 1 to 18 or the anhydrous crystalline form 5 according to any one of claims 19 to 23, wherein said anyhydrous crystalline form has a differential scanning calorimetry thermogram comprising an endotherm with an extrapolated onset temperature between about 159.6 °C and about 169.6 °C.
25. The process according to any one of claims 1 to 18 or the anhydrous crystalline form 10 according to any one of claims 19 to 24, wherein said anyhydrous crystalline form has a thermogravimetric analysis profile showing about 0.5% weight loss below about 135
26. The process according to any one of claims 1 to 18 or the anhydrous crystalline form 15 according to claim 19, wherein said anyhydrous crystalline form has: 1) a powder X-ray diffraction pattern comprising peaks, in terms of 2 , at 8.5° ± 0.2°, and 10.7° ± 0.2°; 2) a differential scanning calorimetry thermogram comprising an endotherm with an extrapolated onset temperature between about 159.6 °C and about 20 169.6 °C; and/or 3) a thermogravimetric analysis profile showing about 0.5% weight loss below about 135 °C.
27. A composition comprising an anhydrous crystalline form of (1aS,5aS)(4-oxy- 25 pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S)hydroxymethyl-2,2-dimethyl-propyl)-amide according to any one of claims 19 to 26.
28. A pharmaceutical composition comprising an anhydrous crystalline form of (1aS,5aS)- 30 2-(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalene carboxylic acid ((S)hydroxymethyl-2,2-dimethyl-propyl)-amide according to any one of claims 19 to 26, and a pharmaceutically acceptable carrier.
29. A dosage form comprising an anhydrous crystalline form of (1aS,5aS)(4-oxy- 35 pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S)hydroxymethyl-2,2-dimethyl-propyl)-amide according to any one of claims 19 to 26, and a pharmaceutically acceptable carrier.
30. A process of making a pharmaceutical composition comprising admixing an anhydrous crystalline form of (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza- cyclopropa[a]pentalenecarboxylic acid ((S)hydroxymethyl-2,2-dimethyl-propyl)- 5 amide according to any one of claims 19 to 26 with a phamaceutically acceptable carrier.
31. A process of making a dosage form comprising admixing an anhydrous crystalline form of (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza- 10 cyclopropa[a]pentalenecarboxylic acid ((S)hydroxymethyl-2,2-dimethyl-propyl)- amide according to any one of claims 19 to 26 with a phamaceutically acceptable carrier.
32. Use of an anhydrous crystalline form according to any one of claims 19 to 26, in the 15 manufacture of a medicament for the treatment of pain.
33. Use of an anhydrous crystalline form according to any one of claims 19 to 26, in the manufacture of a medicament for the treatment of pain; wherein said pain is associated with one or more disorders selected from the group consisting of: bone pain, joint pain, 20 muscle pain, dental pain, migraine pain, headache pain, inflammatory pain, neuropathic pain, pain that occurs as an adverse effect of a therapeutic, osteoarthritis pain, cancer pain, multiple sclerosis pain, allergic reactions, nephritic syndrome, scleroderma, thyroiditis, diabetic neuropathy, fibromyalgia, HIV related-neuropathy, sciatica, and an autoimmune condition.
34. Use of an anhydrous crystalline form according to any one of claims 19 to 26 in the manufacture of a medicament for the treatment of osteoarthritis pain.
35. Use of an anhydrous crystalline form according to any one of claims 19 to 26, in the 30 manufacture of a medicament for the treatment of osteoporosis.
36. An anhydrous crystalline form according to any one of claims 19 to 26, for use in a method of treatment of the human or animal body by therapy. 35
37. An anhydrous crystalline form according to any one of claims 19 to 26, for use in a method of treatment of pain.
38. An anhydrous crystalline form according to any one of claims 19 to 26, for use in the treatment of pain; wherein said pain is associated with one or more disorders selected from the group consisting of: bone pain, joint pain, muscle pain, dental pain, migraine pain, headache pain, inflammatory pain, neuropathic pain, pain that occurs as an adverse 5 effect of a therapeutic, osteoarthritis pain, cancer pain, multiple sclerosis pain, allergic reactions, nephritic syndrome, scleroderma, thyroiditis, diabetic neuropathy, fibromyalgia, HIV related-neuropathy, sciatica, and an autoimmune condition.
39. An anhydrous crystalline form according to any one of claims 19 to 26 for use in the 10 treatment of osteoarthritis pain.
40. An anhydrous crystalline form according to any one of claims 19 to 26, for use in the treatment of osteoporosis. 15
41. A solvate selected from the group consisting of: an acetone solvate of (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a-tetrahydro- 1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S)hydroxymethyl-2,2- dimethyl-propyl)-amide; a non-selective solvate of (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a- 20 tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S) hydroxymethyl-2,2-dimethyl-propyl)-amide; and an ethyl acetate solvate of (1aS,5aS)(4-oxy-pyrazinyl)-1a,2,5,5a- tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalenecarboxylic acid ((S) hydroxymethyl-2,2-dimethyl-propyl)-amide.
42. A composition comprising a solvate according to claim 41.
43. The process according to claim 1 substantially as hereinbefore described with reference to any one of Examples 1-7.
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201161446732P | 2011-02-25 | 2011-02-25 | |
US61/446,732 | 2011-02-25 | ||
US201161448542P | 2011-03-02 | 2011-03-02 | |
US61/448,542 | 2011-03-02 | ||
PCT/US2012/026506 WO2012116276A1 (en) | 2011-02-25 | 2012-02-24 | Crystalline forms and processes for the preparation of condensed azacycles ( cannabinoid receptor modulators) |
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