Compound

Abstract

To provide a hallucinogen with improved oral bioavailability.SOLUTION: The present invention provides a pharmaceutical composition for use in psychedelic-assisted psychotherapy, comprising a compound of formula I in the form of a pharmaceutically acceptable salt [xH is protium or deuterium, n is 1, R1 is the 5-position, R1 is independently selected from -R3, -OR3, and -O(CO) R3, and R2 and R3 are independently selected from C1-C4 alkyl].SELECTED DRAWING: None

Description

FIELD OF THE INVENTION

[0001] The present invention relates to compounds of Formula I, or pharmaceutically acceptable salts thereof, and compositions containing such compounds. These compounds and compositions are used to treat psychiatric or neurological disorders. The compounds of Formula I contain at least one deuterium atom at the α-position, and as a result, have improved oral bioavailability compared to the α-diprotic analogs. [ka] Background of the Invention

[0002] N,N-Dimethyltryptamine (DMT) is an indole alkaloid found endogenously in many species of plants and animals, including humans (SA Barker, EH Mcllhenny, and R. Strassman, Drug Test. Anal., 2012, 4, 617-635). It has a long history of use in Mesoamerican and South American cultures, with archaeological evidence of its use by smoking dating back to c. 2130 BC (CM Torres, Ann. Mus. civ. Rovereto, Sez. Arch., St., Sc. nat., 1995, 11, 291-326). DMT is the hallucinogenic component of the Amazonian concoction ayahuasca, which has been used for centuries in indigenous rituals.

[0003] DMT was first synthesized in 1931 by chemist Richard Manske and then used in research studies by Dr. Stephen Szara during the 1950s, until the illegalization of hallucinogens in the 1960s stopped this line of research. In 1994, Dr. Rick Strassman conducted successful research into DMT, and five studies have been conducted in humans. Further research is currently being conducted at Imperial College London.

[0004] DMT has been shown to be safely administered in humans at doses as low as 0.05 mg / kg and as high as 0.4 mg / kg. Of the five studies conducted since 1994, two used a single bolus injection, one used repeated boluses, and two used a prolonged infusion (over 90-20 minutes). DMT has been found to be well tolerated, with only a few mild to moderate side effects observed, most of which were classified as either negative hallucinogen-like effects or hypertensive responses.

[0005] DMT is a nonselective serotonin receptor agonist with high affinity for the serotonin 5HT2A receptor and is structurally classified as a tryptamine. Recent studies have demonstrated significant therapeutic effects of psilocybin, another tryptamine structurally related to the endogenous neurotransmitter serotonin. The efficacy of psilocybin has been shown in depression (RL Carhart-Harris et al., Psychopharmacology, 2018, 235, 399-408; RL Carhart-Harris et al., Lancet Psychiatry, 2016, 3, 7, 619-627), end-of-life anxiety (RR Griffiths et al., J. Psychopharmacol., 2016, 30, 12, 1181-1197), and addiction (MW Johnson, A. Garcia-Romeu and RR Griffiths, Am.J. Drug Alcohol Abuse, 2017, 43, 1, 55-60), and is currently being investigated for several other mental health disorders rooted in psychologically destructive thought processing patterns (Anorexia Nervosa: NCT#NCT04052568). Evidence from Dr. Carhart-Harris's laboratory has found that psilocybin's mechanism of action shares many similarities with that of DMT.

[0006] Using magnetoencephalography (MEG), electroencephalography (EEG) and functional magnetic resonance imaging (fMRI), Carhart-Harris's group demonstrated hallucinatory states induced by psilocybin (SD Muthukumaraswamy et al., J. Neurosci., 2013, 33, 38, 15171-15183; MM Schartner et al., Sci. Rep., 2017, 7, 46421), LSD (RL Carhart-Harris et al., 2016, 113, 17, 4853-4858; Schartner et al., 2017 (above)) and DMT (C. Timmermann et al., Sci. Rep., 2019, 9, We showed that the entropy of psilocybin (16324) is associated with a decrease in oscillatory power across a range of frequency bands and increases spontaneous signal diversity and global integration of brain networks. This work, summarized in the entropy brain hypothesis (RL Carhart-Harris, Neuropharmacology, 2018, 142, 167-178; RL Carhart-Harris et al., Front. Hum. Neurosci., 2014, 8, 20, 1-22), may explain the antidepressant effects of psilocybin recently reported by this group (RL Carhart-Harris et al., 2018 (supra); RL Carhart-Harris et al., 2016 (supra)).

[0007] An integral feature of the entropy brain hypothesis is the default mode network (DMN), a part of the brain described as a conductor of global brain function (R.L. Carhart-Harris et al., 2014, supra). The DMN is associated with higher-level metacognitive processes, such as thinking about oneself and others (P. Qin and G. Northoff, Neuroimage, 2011, 57, 3, 1221-1233; R.N. Spreng and C.L. Grady, J. Cogn. Neurosci., 2010, 22, 6, 1112-1123), remembering the past, and thinking about the future (R.L. Buckner and D.C. Carroll, Trends Cogn. Sci., 2007, 11, 2, 49-57).

[0008] Brain imaging work has suggested that increased DMN integrity may be a marker of depressed mood, specifically depressive rumination (MG Berman et al., Soc. Cogn. Effect., 2011, 6, 5, 548-55; JP Hamilton at al., Biol. Psychiatry, 2015, 78, 4, 224-230). Under psilocybin (R.L. Carhart-Harris et al., PNAS, 2012, 109, 6, 2138-2143), LSD (R.L. Carhart-Harris et al., 2016, supra), ayahuasca (F. Palhano-Fontes et al., PLOS One, 2015, 10, 2:e0118143), and DMT, a rapid decline in DMN functional integrity was observed, followed by an acute post-treatment increase in its integrity, as shown with psilocybin (R.L. Carhart-Harris et al., 2017, supra). Changes in DMN integrity correlate with improved mood in depressed patients (ibid.). The observed decrease and subsequent increase in DMN integrity is consistent with the hypothesis of a "reset" mechanism, in which acute modular disruption of the DMN allows subsequent reintegration and subsequent normal function (ibid.).

[0009] Antidepressant effects consistent with a resetting mechanism have been supported in multiple studies using psilocybin, as well as in preliminary studies using ayahuasca. In a pilot study by F.L. Osorio et al. (Braz. J. Pschiatry, 2015, 31, 1, 13-20), six volunteers with recurrent MDD were administered a single dose of ayahuasca, which produced rapid antidepressant and anxiolytic effects maintained for up to 21 days. These results were later confirmed in a larger sample by R.F. Sanches et al. (J. Clin. Psychopharmacol, 2016, 36, 1, 77-81). More recently, the antidepressant effects of ayahuasca were tested in a randomized, placebo-controlled trial in 29 patients with TRD (F. Palhano-Fontes et al., 2019, 49, 4, 655-663). Ayahuasca was again found to exert a rapid antidepressant effect that was maintained for up to seven days.

[0010] In addition to evidence from brain activity, the quality of an individual's psychedelic experience has also been linked to treatment outcome. Quality refers to the depth of the psychedelic experience, often described as "mystical" or "spiritual," and is measured using questionnaires such as the Mystical Experiences Questionnaire (MEQ) and the Altered States of Consciousness (ASC) Questionnaire. Numerous studies now show that the intensity of feelings of interconnectedness and oneness, transcendence of time and space, or a sense of wonder predict long-term treatment outcomes with psilocybin across a variety of indications (MP Bogenschutz et al., J. Psychopharmacol., 2015, 29, 3, 289–299; RR Griffiths et al., 2016 (supra); L. Roseman, DJ Nutt, and RL Carhart-Harris, Front. Pharmacol., 2018, 8, 974). DMT experiences score comparable to psilocybin on all such scales (C. Timmermann et al., Front. Psychol., 2018, 9, 1424), further supporting its potential therapeutic benefits.

[0011] Data collected from imagery studies conducted with DMT provide strong evidence that it shares a mechanism of action with psilocybin and allows for the occurrence of a "reset" in the DMN that may facilitate therapeutic effects. This is supported by the antidepressant effects observed in studies with ayahuasca, given that DMT is the main component of the brew that induces a hallucinogenic state.

[0012] Additional preliminary evidence from the Carhart-Harris laboratory demonstrated a reduction in neuroticism scores in ongoing study participants administered DMT. Because depressive symptoms have been shown to be associated with higher scores on neuroticism, trait neuroticism may play an important role in the development of depressive disorders (H. Sauer et al., J. Affect. Disord., 1997, 42, 2-3, 169-177). Rumination has been shown to be an important mediator between this personality trait and depressive disorders, which, as previously mentioned, may be a symptom of an overly rigid DMN. Therefore, DMT may provide a means of reducing neuroticism as part of its therapeutic effect, thereby halting or preventing the onset or continuation of depressive rumination.

[0013] Given the above, there is overwhelming evidence that clinical-grade tryptamines, particularly DMT, should be investigated in large-scale clinical trials for many mental health conditions. However, currently, there are no Good Manufacturing Practice (GMP) providers of DMT or other tryptamine-derived hallucinogens, apart from psilocybin.

[0014] Tryptamine is commonly synthesized using methods adapted from Alexander Shulgin's pioneering publication, *TiHKAL: The Continuation* (Berkeley, CA, Transform Press, 1997). This publication discloses several alternative methods for synthesizing DMT, with a three-step route starting from indole using (1) oxalyl chloride, (2) dimethylamine, and (3) lithium aluminum hydride being widely adopted (see the top synthetic route shown in Scheme 1). A similar route has been used to scale psilocybin under GMP control (see, for example, WO 2019 / 073379A1). Oxalyl chloride is highly toxic and corrosive. It severely irritates the eyes, skin, and respiratory tract and reacts violently with water, making it difficult to handle on a large scale.

[0015] The synthesis of DMT from auxin (a plant hormone and natural product) was reported by P. E. Morris and C. Chiao in J. Lab. Radiopharm., 1993, 33, 6, 455-465 (see the lower synthetic route shown in Scheme 1). Nevertheless, the oxalyl chloride route remains popular due to its high yield compared to other known routes. Therefore, there is a need in the art for an alternative method for synthesizing DMT of Formula I and DMT-type compounds that avoids the problematic use of oxalyl chloride while producing high-purity compounds of Formula I without sacrificing yield.

[0016] 5-Methoxy-N,N-dimethyltryptamine (5-MeO-DMT) is a short-acting psychoactive indole alkylamine found endogenously in Colorado River toad bufotoxin venom (T. Lyttle, D. Goldstein, and J. Gartz, J. Psychoact. Drugs, 1996, 28, 3, 267-290; A.T. Weil and W. Davis, J. Ethnopharmacol., 1994, 41, 1-2, 1-8) and in the seeds of various plant species, including Virola resin, Peregrina, and Dictyoloma incanescens (C.M. Torres and D.B. Repke, Anadenanthera: Fantastic Plants of Ancient South America, 2006, The Haworth Herbal Press, Oxford). 5-MeO-DMT has been reported to have been used by indigenous cultures in the pre-Columbian Americas (T. Weil and W. Davis, 1994, supra) and was first synthetically produced in 1936 (T. Hoshino and K. Shimodaira, Bull. Chem. Soc. Jpn., 1936, 11, 3, 221-224).

[0017] As a structural analog of serotonin, 5-MeO-DMT has affinity for the 5HT1A and 5HT2A receptor pathways, with particularly high affinity for 5HT1A. It also activates 5HT2A, 5HT3A, 5HT5, 5HT6, and 5HT7 receptors (AL Halberstadt and DE Nichols, Handbook of Behavioral Neuroscience, 2010, 21, 621-636; MC McBride, J. Psychoactive Drugs, 2000, 32, 3, 321-331). To a lesser extent, 5-MeO-DMT also activates D1, D3, and alpha-2 receptors (TS Ray, PLOS One, 2010, 5, 2, e9019), and is a ligand for sigma1 receptors (A. Szabo et al., PLOS One, 2014, 9, 8, e106533).

[0018] 5-MeO-DMT is an endogenous tryptamine found in human blood, urine, and spinal fluid (SA Barker, EH McIlhenny, R. Strassman, Drug Test. Anal., 2012, 4, 7-8, 617-635; F. Benington, RD Morin and LC Clark, J. Med. Sci., 1965, 2, 397-403; F. Franzen and H. Gross, Nature, 206, 1052; RB Guchhait., J. Neurochem., 1976, 26, 1, 187-190), and has been shown to exhibit protective and therapeutically relevant effects. Studies by V. Dakic et al., Sci. Rep., 2017, 7, 12863, and A. Szabo et al., PLOS One, 2014, 9, 8, e106533, have shown that 5-MeO-DMT is neuroprotective, anti-inflammatory, and a modulator of both immune responses and human brain cell morphogenesis. Antidepressant properties have been demonstrated in rodents administered 5-MeO-DMT in the form of increased prefrontal theta band activity (MS Riga et al., Neuropharmacology, 2017, 113, A, 148-155). Changes in activity in this region have been attributed to the effectiveness of psilocybin, another hallucinogenic tryptamine, in treating treatment-resistant depression (RL Carhart-Harris et al., 2012, supra).

[0019] 5-MeO-DMT is not orally bioavailable without coadministration with a monoamine oxidase inhibitor. However, inhaled 5-MeO-DMT has been reported to produce potent visual and auditory alterations and alterations in time perception (J. Ott, J. Psychoactive Drugs, 2001, 33, 4, 403-407; Shulgin and Shulgin, 1997, supra), and is rapidly metabolized with a half-life of 12–19 minutes (HW. Shen et al., Curr. Drug. Metab., 2010, 11, 8, 659-666). Experienced users report that inhaling vaporized 5-MeO-DMT produces experiences ranging from spiritual ecstasy and enlightenment to feelings of near-death anxiety and panic (https: / / www.erowid.org / library / books_online / tihkal / tihkal38.shtml, 2018).

[0020] Human EEG studies have shown that vaporized synthetic 5-MeO-DMT (2–5 mg) produces a transient, reversible reorganization of brain network dynamics found in the form of alpha suppression, a shift from alpha to theta activity, increased gamma power, and induced hypercoherence in all bands. Subjects reported feelings of peace, calm, and clarity during the resolution phase (J. Acosta-Urquidi, Cosmos and History: The Journal of Natural and Social Philosophy, 2015, 11, 2, 115–129).

[0021] In an epidemiological study of over 500 people who ingested 5-MeO-DMT in various forms in an uncontrolled setting, many users reported therapeutic benefits attributable to its use (A.K. Davis et al., J. Psychopharmacol., 2018, 32, 7, 779-792). Participants who described having a psychiatric diagnosis indicated improvement in symptoms after 5-MeO-DMT use, including post-traumatic stress disorder (79%), depression (77%), and anxiety (69%). These respondents reported infrequent use (less than once per year) and four or fewer times in their lifetime. Furthermore, 5-MeO-DMT demonstrated a safe profile, as evidenced by low intensity of challenging experiences (e.g., fear, anxiety) and low addictive potential (i.e., very low rates of legal, medical, and psychiatric treatment associated with consumption).

[0022] 5-MeO-DMT has also shown potential for treating substance abuse disorders. Proteomic studies have demonstrated that 5-MeO-DMT exhibits anti-addictive properties due to its ability to downregulate metabotropic glutamate receptor 5 (V. Dakic et al., Sci. Rep., 2017, 7, 12863), which in turn downregulates the rewarding effects of alcohol (M.K. Bird et al., Int. J. Neuropharmacol., 2008, 11, 6, 765-774), cocaine (C. Chiamulera et al., Nat. Neurosci., 2001, 4, 873-874), and nicotine withdrawal (A.K. Stoker, B. Olivier, and A. Markou, Psychopharmacology, 2012, 221, 317-327). Its primary mechanism of therapeutic action is agonism at 5HT1A and 5HT2A receptors, with other classic hallucinogens with similar serotonergic effects (e.g., LSD, psilocybin) consistently demonstrating therapeutic potential in treating alcohol use disorders (FS Abuzzahab and BJ Anderson, Int. Pharmacopsychiatry, 1971, 6, 223-235; TS Krebs and PO Johansen, J. Psychopharmacol., 2012, 26, 7, 994-1002; EM Nielson et al., Front. Pharmacol., 2018, 9, 132).

[0023] DMT, in the form of brewed ayahuasca, has been shown to reduce addictive behaviors in animal models of alcohol dependence by inhibiting behavioral sensitization to alcohol (E.G. Cata-Preta et al., Front. Pharmacol. 2018, 9, 561), which is theorized to be due to the serotonergic properties of this tryptamine (Shen et al., 2010, supra). In the epidemiological survey of 5-MeO-DMT users mentioned above, alcohol-dependent or hazardous drinking individuals (66%, n = 75 of 113) reported improvement after use, suggesting evidence of its potential as a therapeutic agent for alcohol use disorders.

[0024] A strong predictor of treatment efficacy across human treatment studies of various mental health disorders is the occurrence of mystical-type experiences (MP Bogenschutz and MW Johnson, Prog. Neuropsychopharmacol. Biol. Psychiatry, 2016, 64, 4, 250-258; BTH de Veen et al., Expert Rev. Neurother., 2017, 17, 2, 203-212; A. Loizaga-Velder and R. Verres, J. Psychoact. Drugs, 2014, 46, 1, 63-72; Roseman et al., 2018 (supra)). In particular, studies of psilocybin-assisted treatment for alcoholism have consistently identified the intensity of mystical experiences as a significant predictor of outcome (MP Bogenschutz et al., 2015, supra; MP Bogenschutz and MW Johnson, 2016, supra; BTH de Veen et al., 2017, supra). Administered 5-MeO-DMT has been shown to reliably produce mystical-type experiences (Davis et al., 2018, supra) of equal or greater intensity than psilocybin (J. Barsuglia et al., Front. Psychol., 2018, 9, 2459), suggesting that 5-MeO-DMT is likely to have similar, or potentially greater, efficacy than psilocybin in treating substance use disorders. This extends to other disorders for which psilocybin has shown efficacy, including depression (RL Carhart-Harris et al., 2018 (supra); RL Carhart-Harris, et al., 2016 (supra)), end-of-life anxiety (RR Griffiths et al., 2016 (supra)), and other disorders possibly rooted in hallucinogenically destructive patterns (anorexia nervosa: NCT#NCT04052568).

[0025] DMT and its substituted analogs (e.g., 5-MeO-DMT) are inactivated via a deamination pathway mediated by monoamine oxidase (MAO). MAO is found in most cell types in the body. Therefore, DMT and its substituted analogs (e.g., 5-MeO-DMT) are often administered with MAO inhibitors (MAOIs) to prevent inactivation of the compounds before they reach their target sites in the body, allowing for extended exposure to the compounds. As noted above, 5-MeO-DMT is not orally bioavailable without coadministration with an MAOI. However, MAOIs can cause hypertension when ingested with certain foods or medications. For this reason, MAOI use by patients typically requires the patient to restrict their diet and avoid certain other medications.

[0026] In light of the therapeutic potential of substituted dialkyltryptamines such as 5-MeO-DMT, there remains a need in the art for such compounds with improved oral bioavailability, extended and / or modified pharmacokinetics, particularly for the development of clinically applicable psychedelic drugs that can avoid the use of MAOIs and aid in psychotherapy. The present invention addresses this need. SUMMARY OF THE INVENTION

[0027] The present invention relates to a compound of formula I or a pharmaceutically acceptable salt thereof, wherein: x H, n, R 1 and R 2 is defined below. [ka]

[0028] As mentioned above, 5-MeO-DMT is not orally bioavailable unless co-administered with an MAOI. The compound of formula I contains at least one deuterium atom at the α-position. The inventors have surprisingly found that such compounds are metabolized more slowly than their α-dipeptide analogs, resulting in improved oral bioavailability. The compound of formula I is a potent tryptamine hallucinogen with therapeutic applications in psychiatric or cognitive disorders.

[0029] Thus viewed from a first aspect, there is provided a compound of formula I, or a pharmaceutically acceptable salt thereof, for use in therapy. [ka] At this time, x H is protium or deuterium, n is selected from 1, 2, 3, or 4; R 1 -R 3 , -OR 3 , -O(CO)R 3 , -F, -Cl, -Br, or -I; R 2 and R 3 is independently selected from C1-C4 alkyl. Viewed from a second aspect, there is provided a compound as defined in the first aspect, or a pharmaceutically acceptable salt thereof, wherein n is 1 and R 1 When is 5-methoxy, one x H is deuterium and the others are protium.

[0030] The inventors have applied knowledge of the kinetic isotope effects exhibited by the compounds of the present invention to controllably modify the pharmacokinetic profile of the compounds, thereby enabling more flexible therapeutic applications. In particular, the compounds of the present invention can be manufactured by providing individual drug substance compositions containing mixtures of the compounds of the present invention and their non-deuterated analogs. Such compositions can enable fine-tuned single doses to maintain patients completely disconnected from the outside world for a therapeutically optimized duration, without relying on infusion protocols or combination therapy with monoamine oxidase inhibitors in clinical settings.

[0031] The inventors have observed a quantitative relationship between the degree of deuteration and the enhancing effect on the metabolic half-life of the parent compound. This technical effect can be used to quantitatively increase the precision with which compositions containing multiple compounds of Formula I can be prepared. A "composition containing multiple compounds of Formula I" refers to a composition containing at least a first and a second compound, where the first compound is a compound of Formula I and the second compound is a non-deuterated analog of the first compound. For example, the first compound may be α-deutero-5-methoxydimethyltryptamine, in which case the second compound is 5-methoxydimethyltryptamine.

[0032] Viewed from a third aspect, there is therefore provided a composition comprising at least a first and a second compound, or a pharmaceutically acceptable salt thereof, wherein the first compound is selected from the compounds defined in the first or second aspect, and the second compound is a non-deuterated analogue of the first compound.

[0033] Viewed from a fourth aspect, there is provided a pharmaceutical composition comprising a compound as defined in the first or second aspect, a pharmaceutically acceptable salt thereof, or a composition of the third aspect, in combination with a pharmaceutically acceptable excipient.

[0034] As noted above, the compounds and compositions of the invention have use in the treatment of psychiatric or neurological disorders. Viewed from the fifth aspect, therefore, there is provided a composition of the third or fourth aspect for use in therapy.

[0035] Viewed from a sixth aspect, there is provided a compound as defined in the first or second aspect, a pharmaceutically acceptable salt thereof, or a composition of the third or fourth aspect, for use in a method of treating a psychiatric or neurological disorder in a patient.

[0036] Viewed from a seventh aspect, there is provided a method of treatment comprising administering to a patient in need thereof a compound as defined in the first or second aspect, a pharmaceutically acceptable salt thereof, or a composition of the third or fourth aspect.

[0037] As mentioned above, the compounds of the present invention have improved oral bioavailability. Viewed from an eighth aspect, there is therefore provided an oral dosage form comprising a compound defined in the first or second aspect, a pharmaceutically acceptable salt thereof, or a composition of the third or fourth aspect.

[0038] Further aspects and embodiments of the present invention will become apparent from the discussion that follows. [Brief explanation of the drawings]

[0039] [Figure 1] FIG. 1 shows known synthetic routes for the preparation of DMT-type compounds. [Figure 2] Figure 2 shows predicted pharmacokinetic profiles of partially deuterated and fully deuterated drug substances of the compound of Formula I compared to non-deuterated drug substances of the compound of Formula I. The predicted A) plasma concentrations and B) brain tissue concentrations indicate an extended half-life of partially deuterated DMT. The shaded area indicates the effect-site concentration experienced upon complete dissociation from the environment. [Figure 3]Figure 3 is a plot of calculated in vitro half-lives for DMT and the hexadeuterated composition described in Example 4. A) Linear regression analysis. The r value for half-life was 0.754 and the slope was found to be significantly different from 0, p=0.01. B) Half-lives of deuterated analogs as percent change from (undeuterated) DMT (dashed line). [Figure 4] Figure 4 shows the in vitro intrinsic clearance for DMT and the hexadeuterated composition described in Example 4. A) Linear regression analysis. The r value for intrinsic clearance was 0.7648 and the slope was found to be significantly different from 0, p=0.01. B) Intrinsic clearance of the deuterated analog as a percent change from (undeuterated) DMT (dashed line). Detailed Description of the Invention

[0040] Throughout this specification, one or more aspects of the present invention may be combined with one or more features described herein to define separate embodiments of the present invention.

[0041] In the following discussion, reference will be made to a number of terms that shall be understood to have the meanings provided below, unless the context clearly indicates otherwise. The nomenclature used herein to define compounds, particularly those described herein, is intended to be in accordance with the rules of the International Union of Pure and Applied Chemistry (IUPAC) for chemical composition, particularly the "IUPAC Compendium of Chemical Terminology (Gold Book)" (see AD Jenkins et al., Pure & Applied Chem., 1996, 68, 2287-2311). For the avoidance of doubt, in the event that the rules of the IUPAC organization are contrary to the definitions provided herein, the definitions herein shall prevail.

[0042] As used herein, singular nouns include plural nouns and vice versa, unless the context requires otherwise.

[0043] Throughout this specification, variations such as "comprise" or "comprising" will be understood to mean the inclusion of a stated element, integer or step, or group of elements, integers or steps, but the exclusion of any other element, integer or step, or group of elements, integers or steps. The term "comprising" encompasses the term "consisting of."

[0044] The term "consisting of" or variations thereof should be understood to mean the inclusion of the stated elements, integers or steps, or groups of elements, integers or steps, to the exclusion of any other elements, integers or steps, or groups of elements, integers or steps.

[0045] In qualifying numbers or values, the term "about" is used herein to refer to a value that is within ±5% of the specified value. For example, a ratio of coupling agent to compound of Formula I of about 1:1 to about 1.5:1 includes ratios of 0.95:1 to 1.575:1.

[0046] The term "hydrocarbyl" defines a monovalent group derived from a hydrocarbon by removing a hydrogen atom from any carbon atom, where the term "hydrocarbon" refers to a compound consisting only of hydrogen and carbon. When a hydrocarbyl is disclosed as optionally containing one or more heteroatoms, any carbon or hydrogen atom on the hydrocarbyl may be replaced with a heteroatom or a functional group containing a heteroatom to satisfy the valence. The one or more heteroatoms may be selected from the group consisting of nitrogen, sulfur, and oxygen.

[0047] Oxygen and sulfur heteroatoms or functional groups, including these heteroatoms, can replace -H or -CH2- in hydroxycarbyls, provided that when -H is replaced, the oxygen or oxygen-containing functional group is attached to the carbon originally bonded to -H as =0 (replacing two -H) or -OH (replacing one -H), and the sulfur or sulfur-containing functional group is attached to the carbon originally bonded to -H as either =S (replacing two -H) or -SH (replacing one -H). When methylene (-CH2-) is replaced, the oxygen is attached to the carbon originally bonded to -CH2- as -O-, and the sulfur is attached to the carbon originally bonded to -CH2- as -S-.

[0048] The nitrogen heteroatom or functional group containing the nitrogen heteroatom may be substituted with -H, -CH2-, or -CH=, provided that when -H is substituted, the nitrogen or nitrogen-containing functional group is attached to the carbon originally bonded to -H as a triple bond N (replacing three -H), =NH (replacing two -H), or -NH2 (replacing one -H); when -CH2- is substituted, the nitrogen or nitrogen-containing functional group is attached to the carbon originally bonded to -CH2- as -NH-, and when -CH= is substituted, the nitrogen is attached to the carbon originally bonded to -CH= as -N=.

[0049] The term "alkyl" is well known in the art and defines a monovalent group derived from an alkane by removing a hydrogen atom from any carbon atom, where the term "alkane" refers to a group of the general formula C n H 2n+2 where n is an integer ≧1. C1-C4 alkyl means any one selected from the group consisting of methyl, ethyl, n-propyl, iso-propyl, n-butyl, sec-butyl, iso-butyl and tert-butyl.

[0050] The term "cycloalkyl" defines all monovalent groups derived from a cycloalkane by removing a hydrogen atom from a ring carbon atom. The term "cycloalkane" defines saturated monocyclic and polycyclic branched or unbranched hydrocarbons, where monocyclic cycloalkanes have the general formula C n H 2n where n is an integer ≧3. Typically, the cycloalkyl is a C5-C6 cycloalkyl such as cyclopentyl or cyclohexyl.

[0051] The term "alkylamino" refers to an alkyl group in which any one hydrogen atom is replaced with a primary (-NH), secondary (-NRH), or tertiary (-NR) amino group, where R or each R is independently a hydrocarbyl group. Typically, any one hydrogen atom is replaced with a tertiary amino group, where each R is independently a C-C alkyl.

[0052] The compound defined in the first aspect and the compound defined in the second aspect are useful for treatment and can be administered to a patient in need thereof. As used herein, the term "patient" preferably refers to a mammal. Typically, the mammal is a human, but can also refer to a domestic mammal. This term does not include laboratory mammals.

[0053] The terms "treatment" and "therapy" define the therapeutic treatment of a patient to reduce or stop the rate of progression of, or to ameliorate or cure, a disease. Also included is prevention of a disease as a result of treatment or therapy. Reference to prevention is intended not to require complete prevention of a disease: instead, its progression may be inhibited through treatment or therapy according to the present invention. Typically, treatment or therapy is not prophylactic, and a compound or composition is administered to a patient with a diagnosed or suspected disease.

[0054] Psychedelic-assisted psychotherapy refers to the treatment of mental illness by hallucinogenic means, augmented by one or more protocols in which the patient undergoes a hallucinogenic experience. A hallucinogenic experience is characterized by striking a previously unknown aspect of the mind and may include one or more altered perceptions of hallucinations, empathy, altered states of cognitive or focused consciousness, altered thought patterns, ecstatic or hypnotic states, and streaky states.

[0055] As understood in the art, mental dementia, psychiatric illness or neurological illness is an illness that may be associated with one or more cognitive disorders. As used herein, the term "psychiatric disorder" refers to a clinically significant behavioral or hallucinatory syndrome or pattern that occurs in an individual and is associated with current distress (e.g., painful symptoms) or illness (i.e., illness in one or more significant areas), or is associated with significant increases in death, pain, disruption, or significant loss of important degrees of freedom.

[0056] The diagnostic criteria for the psychiatric or neurological disorders referenced herein are set forth in the Diagnostic and Statistical Manual of Mental Disorders, 5th Edition, (DSM-5).

[0057] As used herein, the term "obsessive-compulsive disorder" (OCD) is defined by the presence of either obsessions or compulsions, but commonly both. Symptoms can cause significant functional impairment and / or distress. An obsession is defined as an unwanted, intrusive thought, image, or urge that repeatedly enters a person's mind. A compulsion is a repetitive behavior or mental act that a person feels driven to perform. OCD typically manifests as one or more obsessions that drive the adoption of the obsession. For example, an obsession with germs may drive a urge to clean, or an obsession with food may drive a urge to overeat, binge eat, or vomit after eating (i.e., a food obsession may manifest as an eating disorder). Compulsions may be overtly observable by others, such as making sure the door is locked, or they may be hidden mental acts that cannot be observed, such as repeating certain phrases in one's mind.

[0058] The term "eating disorder" includes anorexia nervosa, bulimia nervosa, and binge eating disorder (BED). Symptoms of anorexia nervosa include eating too little and / or exercising too much in order to keep weight as low as possible. Symptoms of bulimia nervosa include eating a lot of food in a very short period of time (i.e., binge eating) and preventing weight gain by intentionally making oneself sick, using laxatives, overeating, or overexercising. Symptoms of BED include regularly eating large amounts of food until one feels uncomfortably full and then feeling upset or guilty as a result.

[0059] As used herein, the term "depressive disorder" includes major depressive disorder, persistent depressive disorder, bipolar disorder, bipolar depression, and end-stage depression.

[0060] As used herein, the term "major depressive disorder" (MDD, also referred to as major depression or clinical depression) is defined as the presence of five or more of the following symptoms for a period of two weeks or more (also referred to herein as a "major depressive episode"), present for most of the day, nearly every day: · Depressed moods such as sadness, emptiness, tearfulness (in children and teenagers, depressed moods may manifest as constant irritability); ·Significantly decreased interest in or pleasure from all or most activities; · Significant weight loss, weight gain, or increased or decreased appetite when not dieting (in children, not gaining weight as expected); Insomnia or increased need to sleep; · Either restlessness or slowness of behavior that can be observed by others; · Fatigue or loss of energy; · Feelings of worthlessness or excessive or inappropriate guilt; · Problems with decision-making or problems thinking or concentrating; · Recurring thoughts of death, suicide, or attempted suicide.

[0061] At least one of the symptoms must be depressed mood or loss of interest or pleasure.

[0062] Persistent depressive disorder, also known as dysthymia, is defined as a patient exhibiting two characteristics: A. Depressed mood most of the time, almost every day, for at least two years. Children and adolescents may experience irritable moods, and the time frame is at least one year. B. While depressed, a person experiences at least two of the following symptoms: Overeating or loss of appetite. Sleeping too much or having difficulty sleeping. · Fatigue, lack of energy. ·Lack of self-esteem. · Difficulty concentrating or making decisions.

[0063] As used herein, the term "treatment-resistant major depressive disorder" refers to MDD that fails to achieve an adequate response to adequate treatment with standard of care therapies.

[0064] As used herein, "bipolar illness," also known as manic depression, is a disorder that causes abnormal changes in mood, energy, activity level, and ability to carry out daily tasks.

[0065] There are two defined subcategories of bipolar illness, all of which involve distinct shifts in mood, energy, and activity levels. These moods range from periods of very "up," elated, and energetic behavior (known as manic episodes, further defined below) to periods of very sad, "down," or hopelessness (known as depressive episodes). Less severe manic periods are known as hypomanic episodes.

[0066] Bipolar I Disorder is defined by a manic episode lasting at least 7 days or manic symptoms severe enough that the person requires immediate medical care. Depressive episodes usually also occur, usually lasting at least 2 weeks. Depressive episodes with mixed features (simultaneous depressive and manic symptoms) can also occur.

[0067] Bipolar II Disorder is defined by a pattern of depressive and hypomanic episodes, but not the full-blown manic episodes described above.

[0068] As used herein, "bipolar depression" is defined as an individual experiencing depressive symptoms accompanied by a previous or coexisting episode of manic symptoms, but who does not meet the clinical criteria for bipolar disorder.

[0069] As used herein, the term "anxiety disorders" includes generalized anxiety disorder, phobias, panic disorders, social anxiety disorders, and post-traumatic stress disorder.

[0070] As used herein, "generalized anxiety disorder" (GAD) refers to a chronic illness characterized by long-term anxiety that is not focused on any particular object or situation. People suffering from generalized anxiety disorder experience persistent, nonspecific fears and worries and become excessively concerned about everyday things. GAD is characterized by chronic excessive distress accompanied by three or more of the following symptoms: restlessness, fatigue, problems concentrating, irritability, muscle tension, and sleep disturbances.

[0071] "Phobia" is defined as a persistent fear of an object or situation that the affected person will go to great lengths to avoid, usually out of proportion to the danger it poses. If the feared object or situation cannot be completely avoided, the affected person will endure it with marked distress and significant interference with social or occupational activities.

[0072] A patient suffering from "panic disorder" is defined as one who experiences one or more brief attacks of intense fear and anxiety (also known as panic attacks), often accompanied by trembling, shaking, confusion, dizziness, nausea, and / or difficulty breathing. A panic attack is defined as a feeling of fear or discomfort that occurs suddenly and peaks within 10 minutes.

[0073] "Social anxiety disorder" is defined as an intense fear and avoidance of negative public scrutiny, embarrassment, humiliation, or social interactions. Social anxiety often manifests as specific physical symptoms, such as blushing, sweating, and difficulty speaking.

[0074] Post-traumatic stress disorder (PTSD) is an anxiety disorder that results from a traumatic experience. Post-traumatic stress can result from extreme situations such as combat, natural disasters, rape, hostage situations, child abuse, bullying, or even a serious accident. Common symptoms include hypervigilance, flashbacks, avoidant behavior, anxiety, anger, and depression.

[0075] As used herein, the term "postpartum depression" (PPD, also known as postnatal depression) refers to a form of depression experienced by either parent of a newborn. Symptoms typically begin within four weeks after birth and may include extreme sadness, fatigue, anxiety, loss of interest or pleasure in hobbies and activities, irritability, and changes in sleeping and eating patterns.

[0076] As used herein, the term "drug abuse" means a patterned use of a drug in which the user consumes the substance in amounts or in ways that are harmful to themselves or others.

[0077] As used herein, the term "anxiety disorder" refers to a disorder that includes as a symptom a decreased motivation to initiate and perform independent, purposeful activity.

[0078] "LiAl x H4" is lithium aluminum hydride, which is a reducing agent (a chemical that can reduce the oxidation level of organic compounds), and when x is 1, x H is protium (hydrogen with atomic weight 1) or deuterium lithium aluminum, when x is 2, x H should be understood to mean deuterium (hydrogen with an atomic weight of 2). According to some embodiments, "LiAl x "H4" means LiAlD4 or LiAlH4 and LiAlD4. According to some embodiments, "LiAl x"H4" is LiAlD4, optionally containing 0.1 to 99.9% LiAlH4. Stage 2 of the methods disclosed herein involves reacting a compound of formula II with LiAlD4 or LiAlH4 and LiAlD4, i.e., LiAlD4 or a mixture of LiAlH4 and LiAlD4 can be reacted with a compound of formula II. A mixture of 2% to 98% lithium aluminum hydride or 2% to 98% lithium aluminum hydride can be used.

[0079] Unless the context indicates otherwise, amine means a secondary amine.

[0080] High-performance liquid chromatography (HPLC) is a technique in analytical chemistry used to separate, identify, and quantify components in a mixture. For a review of HPLC, see AM Sabir et al., Int. Res. J. Pharm., 2013, 4, 4, 39-46.

[0081] As used herein, solvents include MeCN (acetonitrile), DCM (dichloromethane), acetone, IPA (isopropyl alcohol), iPrOAc (isopropyl acetate), TBME (t-butyl methyl ether), THF (tetrahydrofuran), 2-MeTHF (2-methyltetrahydrofuran), EtOAc (ethyl acetate), ethanol, and toluene. As used herein, the term ethereal solvent refers to a solvent containing an alkyl-O-alkyl moiety, where the two alkyl components may be linked. Ethereal solvents include diethyl ether, TBME, THF, and 2-MeTHF.

[0082] A desiccant is a chemical used to remove water from organic compounds in solution. Examples of desiccants include calcium chloride, magnesium sulfate, and sodium sulfate. The desiccant described herein is typically magnesium sulfate.

[0083] Suitable acidic agents for crystallizing pharmaceutically acceptable salts of compounds of Formula I are acids that form non-toxic acid anions, examples of which include hydrochloride, hydrobromide, sulfate, phosphate or acid phosphate, acetate, maleate, fumarate, lactate, tartrate, citrate, and gluconate.

[0084] By aqueous basic solution is meant a mild base suitable for work-up, such as 10% potassium carbonate solution.

[0085] As noted above, the present invention provides in a first aspect a compound of formula I, or a pharmaceutically acceptable salt thereof, for use in therapy. [ka] During the ceremony, x H is protium or deuterium, n is selected from 1, 2, 3 or 4; R 1 -R 3 , -OR 3 , -O(CO)R 3 , -F, -Cl, -Br, or -I; and R 2 and R 3 is independently selected from C1-C4 alkyl. R 2 are independently selected from C1-C4 alkyl, and often independently selected from methyl or ethyl. In some embodiments, R 2 is methyl. R 1 -R 3 , -OR 3 , -O(CO)R 3 , -F, -Cl, -Br, or -I, and R 3 is selected from C1-C4 alkyl. Often, R 1 -OR 3 , and -O(CO)R 3 are independently selected from 3 is methyl or ethyl. In some embodiments, R3 is methyl. In some embodiments, R 1 is methoxy or acetoxy, for example methoxy.

[0086] In some embodiments, n is 1 to 4, and in some embodiments, when n is >1, at least one R 1 is in fourth or fifth place.

[0087] In some embodiments, n is 0 or 1. In some embodiments, n is 0. In other embodiments, n is 1. In some embodiments, n is 1 and R 1 is in fourth or fifth place.

[0088] In some embodiments, n is 1 and R 1 HA-OR 3 and -O(CO)R 3 is selected from, typically R 3 is methyl. Often, R 1 HA-OR 3 and typically R 3 is methyl (i.e., R 1 is often OMe).

[0089] In some embodiments, when n is 1, R 1 is selected from 4-methoxy (4-MeO), 5-MeO, 4-acetoxy (4-AcO), and 5-AcO, such as 5-methoxy.

[0090] In some embodiments, x H is deuterium.

[0091] In a more particular embodiment of the first aspect, the compound of formula I is α,α-dideutero-5-methoxydimethyltryptamine.

[0092] Methods for preparing compounds of Formula I are described below and are suitable for preparing highly pure compounds of Formula I. In some embodiments, the compound of Formula I, or a pharmaceutically acceptable salt thereof, is between 99% and 100% pure by HPLC, e.g., between 99.5% and 100% pure by HPLC. In some embodiments, the compound of Formula I, or a pharmaceutically acceptable salt thereof, is between 99.9% and 100% pure by HPLC, e.g., between 99.95% and 100% pure by HPLC.

[0093] In some embodiments, the compound of Formula I or a pharmaceutically acceptable salt thereof produces two or fewer impurity peaks by HPLC. In some embodiments, the compound of Formula I or a pharmaceutically acceptable salt thereof produces impurity peaks by HPLC, and the impurity peaks do not exceed 0.2%. In some embodiments, the impurity peaks do not exceed 0.1% by HPLC.

[0094] In some embodiments, the compound of Formula I is in the form of a pharmaceutically acceptable salt. The pharmaceutically acceptable salt often consists of a compound of Formula I and a suitable acid. The compound of Formula I is typically represented by the group —N(R 2 )2 and protonated at -[NH(R 2 )2] + and the resulting positive charge is counterbalanced by an anion.

[0095] P.H. Stahl and C.G. Wermuth provide an overview of pharmaceutical salts and acids contained therein in Handbook of Pharmaceutical Salts: Properties, Selection and Use, Weinheim / Zuerich:Wiley-VCH / VHCA, 2002. The acids described herein are suitable components of pharmaceutically acceptable salts of Formula I.

[0096] In some embodiments, the acid is fumaric acid, tartaric acid, citric acid, hydrochloric acid, acetic acid, lactic acid, gluconic acid, 1-hydroxy-2-naphthoic acid, 2,2-dichloroacetic acid, 2-hydroxyethanesulfonic acid, 2-oxoglutaric acid, 4-acetamidobenzoic acid, 4-aminosalicylic acid, adipic acid, ascorbic acid, aspartic acid, benzenesulfonic acid, benzoic acid, camphoric acid, camphor-10-sulfonic acid, decanoic acid, hexanoic acid, octanoic acid, carbonic acid, cinnamic acid, cyclamic acid, dodecyl sulfuric acid, ethane-1,2-disulfonic acid, ethanesulfonic acid, formic acid, galactaric acid, gentisic acid, glucoside, or the like. Heptonic, glucuronic, glutamic, glutaric, glycerophosphoric, glycolic, hippuric, hydrobromic, isobutyric, lactobionic, lauric, maleic, malic, malonic, mandelic, methanesulfonic, naphthalene-1,5-disulfonic, naphthalene-2-sulfonic, nicotinic, nitric, oleic, oxalic, palmitic, pamoic, phosphoric, propionic, pyroglutamic (-L), salicylic, sebacic, stearic, succinic, sulfuric, thiocyanic, toluenesulfonic, and undecylenic acids.

[0097] Often, the acid is any one selected from fumaric acid, tartaric acid, citric acid, and hydrochloric acid, hi some embodiments, the acid is fumaric acid, i.e., the pharmaceutically acceptable salt is a fumarate salt.

[0098] As noted above, the present invention provides in a second aspect a compound of formula I, or a pharmaceutically acceptable salt thereof: [ka] At this time, x H is protium or deuterium, n is selected from 1, 2, 3, or 4; R 1 -R 3 , -OR 3 , -O(CO)R 3 , -F, -Cl, -Br, or -I; and R 2 and R 3 are independently selected from C1-C4 alkyl, provided that n is 1 and R 1 When is 5-methoxy, one x H is deuterium and the others are protium.

[0099] For the avoidance of doubt, embodiments of the first aspect of the invention relating to compounds of formula I, or pharmaceutically acceptable salts thereof, also apply mutatis mutandis to the second aspect, wherein n is 1 and R 1 When is 5-methoxy, one x H is deuterium and the other is protium. For example, R 2 may be methyl, and R 1 may be methoxy or acetoxy, and / or n may be 1, R 1 may be in fourth or fifth place.

[0100] Also disclosed herein is a synthetic method for producing a compound of Formula I, or a pharmaceutically acceptable salt thereof, comprising Stage 1 and Stage 2, Stage 1 comprising: (i) reacting a compound of formula III with two or more coupling agents to form an activated compound; (ii) combining the activated compound with a compound of formula (R 2 ) reacting with an amine having 2NH to form a compound of formula II; wherein stage 2 involves reacting a compound of formula II with LiAlD4 or LiAlH4 and LiAlD4. [ka] At this time, x H is protium or deuterium, n is selected from 1, 2, 3, or 4; R 1 -R 3 , -OR 3 , -O(CO)R 3, -F, -Cl, -Br, or -I; and R 2 and R 3 is independently selected from C1-C4 alkyl.

[0101] For the avoidance of doubt, embodiments relating to compounds of formula I, or pharmaceutically acceptable salts thereof, of the first aspect of the invention also apply mutatis mutandis to compounds of formula I (and therefore compounds of formula III and II) of the synthetic methods. For example, R 2 (Thus, the compound of formula II and the compound of formula (R 2 ) the amine having 2NH) may be methyl, and R 1 may be methoxy or acetoxy, and / or n may be 1, R 1 may be in the 4th or 5th position.

[0102] This synthetic method avoids the problematic use of oxalyl chloride and uses compounds of formula III that can be derived from auxin derivatives. High-quality and pure auxins of formula III are commercially available on a large scale and / or can be easily synthesized via the Fischer, Bartoli, Japp-Klingemann, or Larock synthesis (see, e.g., M.B. Smith and J. March, 2020, March's Advanced Organic Chemistry, 8th edition, Wiley, New Jersey). This method is efficient, feasible on a large scale, compatible with Current Good Manufacturing Practices (cGMP), and suitable for producing high-purity compounds of formula I. For example, this method is suitable for producing compounds of formula I at a batch scale ranging from 1 g to 100 kg, with purities greater than 99.9% and overall yields of 65% or greater.

[0103] The compound of formula II can be prepared by reacting a compound of formula III with two or more coupling agents to form an activated compound, and then coupling the activated compound with a compound of formula (R 2 ) NH with an amine. Without wishing to be bound by theory, it is understood that the nitrogen atom of the amine bonds to the carbon atom of the carbonyl of formula III, resulting in the formation of a compound of formula II. For the avoidance of doubt, the R 2 The group is the R 2 Thus, as described above, R in Formula II and Formula I 2 are independently selected from C1-C4 alkyl, often independently selected from methyl or ethyl, and in some embodiments, R 2 is methyl.

[0104] The compound of formula I is prepared by reacting a compound of formula II with LiAlD4 or LiAlH4 with LiAlD4. Without wishing to be bound by theory, it is understood that the hydride or deuterium ion provided by LiAlD4 or LiAlH4 and LiAlD4 bonds to the carbon atom of the carbonyl of formula II, resulting in the formation of the compound of formula I. For the avoidance of doubt, the compound of formula I x The H groups are derived from LiAlD4 or LiAlH4 and the hydride or deuteride ions provided by LiAlD4.

[0105] As mentioned above, this method includes Stage 1 and Stage 2. Stage 1 is as follows: (i) reacting a compound of formula III with two or more coupling agents to form an activated compound; (ii) combining the activated compound with a compound of formula (R 2 ) with an amine having 2NH to form a compound of formula II Includes.

[0106] The term "coupling agent" refers to an agent that promotes a chemical reaction between an amine and a carboxylic acid. The two or more coupling agents can include a carboxylic acid activating agent, i.e., an agent that reacts with the carboxylic acid moiety of Formula III to produce a compound containing an activated moiety derived from the original carboxylic acid moiety that is more reactive with amines than the original carboxylic acid moiety.

[0107] The activated compound is the reaction product of a compound of formula III with two or more coupling agents. When the two or more coupling agents include a carboxylic acid activating agent, the activated compound includes an activating moiety derived from the original carboxylic acid moiety of formula III that is more reactive with amines than the original carboxylic acid moiety.

[0108] Two or more of the coupling agents may include a carboxylic acid activator. Two or more of the coupling agents may include an additive coupling agent.

[0109] An additive coupling agent (also referred to herein as an "additive") is an agent that increases the reactivity of a coupling agent. The additive may be a compound that can react with the reaction product of the reaction product of Formula III with a coupling agent (a product that is a compound containing an activated moiety) to produce a compound that contains a more activated moiety that is more reactive with amines than the original activated moiety.

[0110] The additive can react with the reaction product of the reaction product of Formula III with a coupling agent (a product that is a compound containing an activated moiety) to produce an activated compound that contains a more active moiety that is more reactive with amines than the original activated moiety.

[0111] Often the two or more coupling agents include a carboxylic acid activator and an additive coupling agent.

[0112] At least one of the two or more coupling agents can be selected from the group consisting of carbodiimide coupling agents, phosphonium coupling agents, and 3-(diethoxy-phosphonyloxy)-1,2,3-benzo[d]triazin-4(3H)-one (DEPBT), such as a carbodiimide coupling agent or a phosphonium coupling agent. At least one of the two or more coupling agents can be a carbodiimide coupling agent.

[0113] Carbodiimide coupling agents are coupling agents that contain a carbodiimide group R'-N=C=NR" where R' and R" are hydrocarbyl groups optionally substituted with heteroatoms selected from nitrogen, sulfur, and oxygen, typically nitrogen. Often, R' and R" are independently selected from C1-C6 alkyl, C5-C6 cycloalkyl, C1-C6 alkylamino, and morpholinoC1-C6 alkyl. Frequently, the C1-C6 alkyl is C3 alkyl, the C5-C6 cycloalkyl is cyclohexyl, the C1-C6 alkylamino is dimethylaminopropyl, and / or the morpholinoC1-C6 alkyl is morpholinoethyl.

[0114] The carbodiimide coupling agent may be any selected from the group consisting of dicyclohexylcarbodiimide (DCC), diisopropylcarbodiimide (DIC), (N-(3-dimethylaminopropyl)-N'-ethylcarbodiimide (EDO), and 1-cyclohexyl-(2-morpholinoethyl)carbodiimide metho-p-toluenesulfonate (CMCT). The carbodiimide coupling agent may be any selected from the group consisting of dicyclohexylcarbodiimide (DCC), diisopropylcarbodiimide (DIC), and (N-(3-dimethylaminopropyl)-N'-ethylcarbodiimide (EDC). Often, the carbodiimide coupling agent is N-(3-dimethylaminopropyl)-N'-ethylcarbodiimide (EDC), typically the hydrochloride salt (EDC.HCl). EDC or EDC.HCl are particularly preferred because they are non-toxic and highly water soluble, facilitating their substantially complete removal during the Stage 1 workup and cleaning steps.

[0115] Phosphonium coupling agents contain a phosphonium cation and a counterion, typically a hexafluorophosphate anion. The phosphonium cation has the formula [PR a 3R b ] + In this case, R a is di(C1-C6)alkylamino or pyrrolidinyl, and R b is a halo or hydrocarbyl group optionally substituted with nitrogen and / or oxygen atoms. Often, R b is bromo, benzotriazol-1-yloxy or 7-aza-benzotriazol-1-yloxy.

[0116] The phosphonium coupling agent may be any selected from the group consisting of benzotriazol-1-yloxy-tris(dimethylamino)-phosphonium hexafluorophosphate (BOP), bromo-tripyrrolidino-phosphonium hexafluorophosphate (PyBrOP), benzotriazol-1-yloxy-tripyrrolidino-phosphonium hexafluorophosphate (PyBOP), 7-aza-benzotriazol-1-yloxy-tripyrrolidinophosphonium hexafluorophosphate (PyAOP), and ethylcyano(hydroxyimino)aceto-O2)tri-(1-pyrrolidinyl)-phosphonium hexafluorophosphate (PyOxim).

[0117] At least one of the two or more coupling agents is 1-hydroxybenzotriazole (HOBt), hydroxy-3,4-dihydro-4-oxo-1,2,3-benzotriazine (HOOBt), N-hydroxysuccinimide (HOSu), 1-hydroxy-7-azabenzotriazole (HOAt), ethyl 2-cyano-2-(hydroxymino)acetate (Oxyma Pure), 4-(N,N-dimethylamino)pyridine (DMAP), N-hydroxy-5-norbornene-2,3-dicarboximide (HONB), 6-chloro-1-hydroxybenzotriazole (6-Cl-HOBt), 3-hydroxy-4-oxo-3,4 3-hydroxy-4-oxo-3,4-dihydro-5-azepinebenzo-1,3-diazine (HODhad), 3-hydroxy-4-oxo-3,4-dihydro-5-azepinebenzo-1,3-diazine (HODhad), 3-hydroxy-4-oxo-3,4-dihydro-5-azepinebenzo-1,3-diazine (HODhad).

[0118] At least one of the two or more coupling agents may be an additive coupling agent selected from the group consisting of 1-hydroxybenzotriazole (HOBt), hydroxy-3,4-dihydro-4-oxo-1,2,3-benzotriazine (HOOBt), N-hydroxysuccinimide (HOSu), 1-hydroxy-7-azabenzotriazole (HOAt), ethyl 2-cyano-2-(hydroxymino)acetate (Oxyma Pure), and 4-(N,N-dimethylamino)pyridine (DMAP).

[0119] At least one of the two or more coupling agents may be an additive coupling agent that is 1-hydroxybenzotriazole.

[0120] The two or more coupling agents may be composed of a coupling agent and an additional coupling agent, and the coupling agent and the additional coupling agent may be those described in the above embodiments.

[0121] The advantage of using both the coupling agent and the additive coupling agent is that the coupling agent is a compound of formula III and a compound of formula (R 2 ) is the increased rate of formation of the compound of Formula II from an amine having a 2NH. Furthermore, when an additive coupling agent is used in conjunction with a carbodiimide coupling agent, the possibility of undesired side reactions can be reduced. For example, the reaction of a compound of Formula III with a carbodiimide coupling reagent is prone to form an O-acylisourea, which can undergo rearrangement to form an N-acylurea, a stable compound that is less likely to react with amines. The additive coupling reagent can react with the O-acylurea before rearranging to the N-acylurea, producing a compound that reacts with amines rather than the inactive N-acylurea.

[0122] Thus, the two or more coupling agents may consist of a carbodiimide coupling agent and an additive coupling agent.

[0123] The two or more coupling agents may consist of N-(3-dimethylaminopropyl)-N'-ethylcarbodiimide (EDC), typically the hydrochloride salt (EDC.HCL), and 1-hydroxybenzotriazole (HOBt).

[0124] Often, an excess of coupling agent is used relative to the compound of Formula III, with the ratio of coupling agent to compound of Formula III being from about 1:1 to about 3:1, typically from about 1:1 to about 2:1, and most typically from about 1:1 to about 1.5:1.

[0125] Often, an excess of additional coupling agent is used relative to the compound of Formula III. Sometimes the ratio of additional coupling agent to compound of Formula III is from about 1:1 to about 3:1, typically from about 1:1 to about 2:1, and most typically from about 1:1 to about 1.5:1.

[0126] When the two or more coupling agents include a coupling agent and an additional coupling agent, ratios of coupling agent:compound of Formula III and additional coupling agent:compound of Formula III can be used in the range of about 1:1 to about 1.5:1.

[0127] As described above, Stage 1 involves converting an activated compound (the product of reacting a compound of formula III with two or more coupling agents) into a compound of formula (R 2 ) with an amine having NH to produce a compound of formula II. 2 are independently selected from C1-C4 alkyl. Often, R 2 is independently selected from methyl or ethyl. Typically, R 2 is methyl, i.e. the amine is dimethylamine.

[0128] The ratio of amine to compound of Formula III used in this method is often about ≧1:1. Sometimes the ratio of amine to compound of Formula III is about 1:1 to about 3:1, typically about 1:1 to about 2:1.

[0129] In some cases, Stage 1 further includes isolating the compound of Formula II. Those skilled in the art are familiar with techniques suitable for isolating the compound of Formula II. For example, the compound of Formula II may be extracted into an organic solvent such as dichloromethane or ethyl acetate, washed with an aqueous solution such as an aqueous basic solution, and concentrated. To increase purity, the isolated compound of Formula II may be recrystallized. Those skilled in the art are familiar with techniques suitable for recrystallizing the compound of Formula II. For example, the compound of Formula II can be dissolved in a minimum amount of solvent at a specific temperature (e.g., ambient temperature (e.g., 15-25°C) or at an elevated temperature where heat is applied to the solution), and the resulting solution can be cooled to promote precipitation. Alternatively, or additionally, the volume of the solution can be reduced to promote precipitation, for example, by simple evaporation at ambient temperature and pressure. Alternatively, or additionally, an anti-solvent can be used (in which the compound of Formula II is less soluble than in the solvent already present).

[0130] Isolated compounds of formula II are stable and can be stored as solids in air, for example at about 20° C. They can be stored under inert conditions, for example under nitrogen or argon, or at low temperatures, for example in a refrigerator or freezer, unless necessary.

[0131] Typically, steps (i) and (ii) of Stage 1 are carried out in a suitable solvent. Those skilled in the art can assess which solvents are suitable for these steps. Examples of suitable solvents include dichloromethane (DCM), acetone, isopropyl alcohol (IPA), isopropyl acetate (iPrOAc), tert-butyl methyl ether (TBME), 2-methyltetrahydrofuran (2-MeTHF), and ethyl acetate (EtOAc). In some embodiments, steps (i) and (ii) of Stage 1 are carried out in dichloromethane.

[0132] Stage 1 steps (i) and (ii) are carried out at any suitable temperature, and one of skill in the art can assess which temperatures are appropriate for these steps. Stage 1 steps (i) and (ii) are often carried out at a temperature of about 10° C. to about 30° C. In some embodiments, Stage 1 steps (i) and (ii) are carried out at room temperature (about 20° C.).

[0133] In some cases, stage 1 of the method comprises the following steps: i. contacting a compound of Formula III with between 1 and 1.5 equivalents of an additional coupling agent and between 1 and 1.5 equivalents of a carbodiimide coupling agent to form a first composition; and ii. treating the first composition with a compound of formula (R 2 ) contacting the compound with between 1 and 2 equivalents of an amine having a 2NH to form a second composition.

[0134] Often, 1 g or more, for example, 1 g to 100 kg or 1 g to 1 kg, of a compound of formula III is used in the methods of the invention.

[0135] The contacting of step i and step ii is often carried out in the presence of a first solvent, for example, in the presence of 5 to 20 volumes of the first solvent. The first solvent can be selected from dichloromethane (DCM), acetone, isopropyl alcohol (IPA), isopropyl acetate (iPrOAc), tert-butyl methyl ether (TBME), 2-methyltetrahydrofuran (2-MeTHF), and ethyl acetate (EtOAc). Typically, the first solvent is DCM.

[0136] Often, step i further comprises stirring or agitating the first composition. The first composition may be stirred or agitated for at least 30 minutes, e.g., 30 minutes to 3 hours or 30 minutes to 2 hours, preferably at least 1 hour, e.g., 1 to 3 hours or 1 to 2 hours. The first composition may be maintained at a temperature between 10°C and 30°C.

[0137] The amine of step ii is often dissolved in a solvent such as tetrahydrofuran (THF) or ether prior to contacting. The amine may be present in the solvent at a concentration of about 2 M. Typically, the amine of step ii is dissolved in THF.

[0138] In some cases, step ii further comprises stirring or agitating the second composition. The second composition may be stirred or agitated for at least 30 minutes, e.g., 30 minutes to 3 hours or 30 minutes to 2 hours, preferably at least 1 hour, e.g., 1 to 3 hours or 1 to 2 hours. The second composition may be maintained at a temperature between 10°C and 30°C.

[0139] Step ii may further include contacting the second composition with an aqueous basic solution to form a third composition, for example, contacting the second composition with 2 to 10 volumes of an aqueous basic solution, such as an aqueous solution comprising potassium carbonate.

[0140] Optionally, step ii further comprises stirring or agitating the third composition. The third composition may be stirred or agitated for at least 1 minute, e.g., 1 to 15 minutes or 1 to 10 minutes, preferably at least 5 minutes, e.g., 5 to 15 minutes or 5 to 10 minutes. The third composition may be maintained at a temperature between 10°C and 30°C.

[0141] If the third composition comprises an organic and an aqueous component, step ii may further comprise separating the organic component from the aqueous component. The organic component may be separated from the aqueous component within 8 hours of the contacting in step i.

[0142] In some cases, stage 1 of the method of the present invention comprises the following steps: i. adding to a first vessel at least 1 g of a compound of Formula III and 1 to 1.5 equivalents of an additional coupling agent; ii. adding to a first vessel 5-20 volumes of a first solvent selected from DCM, acetone, IPA, iPrOAc, TBME, 2-MeTHF, and EtOAc; iii. adding 1 to 1.5 equivalents of a carbodiimide coupling agent to a first vessel; iv. stirring the contents of the first container for at least 30 minutes, preferably at least 1 hour (e.g., 1-2 hours), between 10°C and 30°C; v. In a first container, 2 ) adding 1 to 2 equivalents of an amine having 2NH, wherein the amine is preferably dissolved in an ether solvent; vi. further stirring the contents of the first vessel for at least 30 minutes, preferably at least 1 hour (e.g., 1-2 hours), between 10°C and 30°C; vii. adding 2 to 10 volumes of an aqueous basic solution to a first container; viii. further stirring the contents of the first container for at least 1 minute, preferably at least 5 minutes (e.g., 5-10 minutes), between 10°C and 30°C; ix. separating an immiscible organic fraction from the aqueous fraction, wherein the organic fraction comprises a compound of Formula II; x. removing the organic fraction containing the compound of formula II; In this case, steps i. to x. are carried out within a single 8 hour period.

[0143] Often the first solvent is DCM.

[0144] Often the amine is dimethylamine. The amine may be dissolved in THF at a concentration of, for example, 2M.

[0145] Often the aqueous basic solution contains potassium carbonate.

[0146] Optionally, stage 1 of the method of the present invention further comprises the steps of: xi. drying the organic fraction with a drying agent, for example, a drying agent selected from calcium chloride, magnesium sulfate, and sodium sulfate; xii. Filtration of the organic fraction; xiii. concentrating the organic fraction under vacuum, e.g., under a pressure of less than 1 atmosphere; xiv. adding the concentrated organic fraction to a second vessel; xv. adding 2-10 volumes of a second solvent to a second vessel, wherein the second solvent is selected from IPA, EtOAc, iPrOAc, acetonitrile (MeCN), TBME, THF, 2-MeTHF, and toluene; xvi. stirring the contents of the second vessel for at least 1 hour, preferably at least 2 hours (e.g., 2-3 hours), at a temperature between 45°C and 55°C; xvii. cooling the contents of the second vessel to a temperature between 15°C and 25°C; xviii. filtering the contents of the second vessel to obtain a filtrate, wherein the filtrate comprises a compound of Formula II; xix. Dry the filtrate

[0147] The drying agent in step xi is typically magnesium sulfate. Often, the solvent in step xv is selected from TBME and IPA.

[0148] Stage 2 of the process involves reacting a compound of Formula II with LiAlD4 or LiAlH4 and LiAlD4 to produce a compound of Formula I. LiAlD4 or a mixture of LiAlH4 and LiAlD4 can be reacted with the compound of Formula II. In a preferred embodiment, Stage 2 of the process involves reacting a compound of Formula II with a mixture of LiAlH4 and LiAlD4. Such mixtures include LiAlD4 and contain between 0.1 and 99.9% hydride. Mixtures of between 2 and 98% lithium aluminum hydride or between 2 and 98% lithium aluminum deuteride can be used. Sometimes, the mixture of LiAlH4 and LiAlD4 consists essentially of 98% LiAlD4 / 2% LiAlH4. Sometimes such mixtures are essentially 95% LiAlD4 / 5% LiAlH4, 95% LiAlH4 / 5% LiAlH4, 85% LiAlD4 / 15% LiAlH4, 80% LiAlD4 / 20% LiAlH4, 75% LiAlD4 / 25% LiAlH4, 70% LiAlD4 / 30% LiAlH4, 65% LiAlD4 / 35% LiAlH4, 60% LiAlD4 / 40% LiAlH4, 55% LiAlD4 / 45% LiAlH4, 50% LiAlD4 / 50% LiAlH4, 45% LiAlD4 / 55% LiAlH4, 40% LiAlD4 / 60% LiAlH4, 35% LiAlD4 / 65% LiAlH4, 30% LiAlD4 / 75% LiAlH4, 25% LiAlD4 / 75% It consists of LiAlH4, 20% LiAlD4 / 80% LiAlH4, 15% LiAlD4 / 85% LiAlH4, 10% LiAlD4 / 90% LiAlH4, 5% LiAlD4 / 95% LiAlH4, or 2% LiAlD4 / 98% LiAlH4.

[0149] A mixture of LiAlH4 and LiAlD4 consisting essentially of specified proportions of LiAlH4 and LiAlD4 means that the mixture can contain additional components (other than LiAlH4 and LiAlD4), but the presence of these additional components does not substantially affect the essential properties of the mixture. In particular, a mixture consisting essentially of LiAlH4 and LiAlD4 does not contain material amounts of agents deleterious to the reduction of the compound of Formula II to form the compound of Formula I (e.g., material amounts of agents that react with LiAlH4 and LiAlD4, the compound of Formula II, and / or the compound of Formula I in a manner that inhibits the reduction of the compound of Formula II to form the compound of Formula I).

[0150] The amount of LiAlH4 or LiAlD4 contained in the two mixtures depends on the degree of deuteration desired in the compound of formula I. For example, x If a compound of formula I is desired in which H is protium and the other is deuterium, a mixture of 50% LiAlH4 and 50% LiAlD4 is preferred. Alternatively, about half of the compounds contain two deuterium atoms in the α position (i.e., both x H is deuterium), about half of the compounds contain one deuterium atom and one protium atom in the α position (i.e., one x If a mixture of compounds of formula I (where H is deuterium and the other is protium) is desired, a mixture of 25% LiAlH4 and 75% LiAlD4 is preferred.

[0151] The amount of LiAlD4 or LiAlH4 and LiAlD4 used relative to the compound of formula II is often ≦1:1. For the avoidance of doubt, the ratio of LiAlH4 and LiAlD4 to the compound of formula II refers to the total amount of LiAlD4 or LiAlH4 and LiAlD4 used relative to the amount of compound II. Sometimes, the ratio of LiAlD4 or LiAlH4 to the compound of formula II is 0.5:1 to 1:1, e.g., 0.8:1 to 1:1. Typically, the ratio of LiAlH4 and / or LiAlD4 to the compound of formula II is 0.9:1.

[0152] Typically, Stage 2 of this process is carried out in a suitable solvent. One skilled in the art can assess which solvent is suitable for Stage 2. Examples of suitable solvents include THF and ethers such as diethyl ether. Often, Stage 2 is carried out in THF.

[0153] Often, LiAID4 or LiAlH4 and LiAlD4 are provided as a solution or suspension of LiAID4 or LiAlH4 and LiAlD4 in a suitable solvent such as an ether, for example THF or diethyl ether, typically THF.

[0154] Stage 2 of the process is carried out at any suitable temperature, and one of skill in the art can assess which temperatures are appropriate for these steps. Often, Stage 2 is carried out at a temperature of from about -5°C to about 65°C.

[0155] Typically, Stage 2 generally further comprises isolating the compound of Formula I. Those skilled in the art will know techniques suitable for isolating the compound of Formula I. For example, upon quenching the reaction (e.g., using an aqueous solution of a tartrate salt such as Rochelle's salt), the compound of Formula I can be extracted into an organic solvent such as ether, e.g., THF or diethyl ether, washed with an aqueous solution such as an aqueous basic solution, and concentrated. The isolated compound of Formula I may be recrystallized. Those skilled in the art will know techniques suitable for recrystallizing the compound of Formula I. The recrystallization techniques described for the recrystallization of the compound of Formula II are applicable, mutatis mutandis, to the recrystallization of the compound of Formula I.

[0156] Often, about 1 g or more, for example, about 1 g to about 100 kg or about 1 g to about 1 kg, of a compound of formula II is used in the methods of the invention.

[0157] Typically, stage 2 of the process involves contacting a compound of formula II with about 0.8 to about 1 equivalent, for example about 0.9 equivalents, of LiAlD4 or LiAlH4 and LiAlD4 to form a first composition.

[0158] The contacting is typically carried out in the presence of a solvent such as an ether, for example THF or diethyl ether, typically THF.

[0159] Often, this contacting involves dropwise addition of LiAlD4 or LiAlH4 and LiAlD4 to the compound of Formula II, where LiAlD4 or LiAlH4 and LiAlD4 are provided as a solution or suspension of LiAlD4 or LiAlH4 and LiAlD4 in a suitable solvent such as an ether, e.g., THF or diethyl ether. LiAlD4 or LiAlH4 and LiAlD4 can be provided as a 2.4 M or 2 M solution or suspension of LiAlD4 or LiAlH4 and LiAlD4 in THF. Sometimes, LiAlD4 or LiAlH4 and LiAlD4 are provided as a 2 M solution or suspension of LiAlD4 or LiAlH4 and LiAlD4 in THF.

[0160] The contacting is often carried out at a temperature of from about -5°C to about 65°C.

[0161] Often, stage 2 further comprises stirring or agitating the first composition. The first composition may be stirred or agitated for about 1 hour to about 6 hours, typically about 2 hours. The first composition may be stirred or agitated at a temperature of about 55°C to about 65°C. Often, the first composition is stirred or agitated at a temperature of about 55°C to about 65°C, and then cooled to a temperature of about 10°C to about 30°C.

[0162] Typically, the compound of formula II is contacted with about 0.9 equivalents of LiAlD4 or LiAlH4 and LiAlD4.

[0163] Stage 2 of the method of the present invention may comprise the following steps: i. adding 1 g or more (e.g., 1 g to 1 kg) of a compound of Formula II to a third container; ii. In a third vessel, add 5-20 volumes of ether solvent; iii. adding to a third vessel a solution of 0.8-1 equivalents of LiAlD4 or LiAlH4 and LiAlD4 in an ethereal solvent dropwise over a period of at least 15 minutes (e.g., 15-30 minutes) at a temperature between -5°C and 65°C; iv. stirring the contents of the third vessel at between 55°C and 65°C for 1 hour to 6 hours, preferably 2 hours; v. Cooling the contents of the third container to 10°C to 30°C; The contents of the third container then comprise the compound of Formula I.

[0164] Often, the ether solvent is THF. Typically, 0.9 equivalents of LiAlD4 or LiAlH4 and LiAlD4 are added to the third vessel in step iii. The LiAlD4 or LiAlH4 and LiAlD4 are typically added to the third vessel as a 2.4 M or 2 M solution in THF. Sometimes, the LiAlD4, LiAlH4, or LiAlD4 is added to the third vessel as a 2 M solution in THF.

[0165] Sometimes, stage 2 of the method involves post-processing, which includes the following steps: vi. Adding 5-20 volumes of an aqueous solution of tartrate (e.g., Rochelle's salt) to a fourth container; vii. adding a composition comprising the crude compound of Formula I to a fourth vessel over a period of at least 15 minutes (e.g., 15 minutes to 1 hour), preferably at least 30 minutes (e.g., 30 minutes to 1 hour) at 15°C to 25°C; viii. Stir the contents of the fourth vessel between 15°C and 25°C for at least 30 minutes (e.g., 30 minutes to 1 hour).

[0166] For the avoidance of doubt, reference to the composition comprising the crude compound of formula I refers to the contents of the third vessel upon completion of step v of stage 2 above.

[0167] Stage 2 of the method may further comprise the steps of: ix. separating the organic fraction from the aqueous fraction, wherein the organic fraction comprises the compound of Formula I; x. removing the aqueous fraction from the fourth container; xi. Add 5 to 20 volumes of brine solution to a fourth container; xii. stirring the contents of the fourth vessel for at least 5 minutes (e.g., 5-15 minutes) at a temperature between 15°C and 25°C; xiii. removing the organic fraction containing the compound of formula I as a free base; xiv. drying the organic fraction with a drying agent, for example, a drying agent selected from calcium chloride, magnesium sulfate, and sodium sulfate; xv. filtering the organic fraction, and xvi. The organic fraction is concentrated under vacuum, for example, under a pressure less than 1 atmosphere.

[0168] The isolated compound of formula I (prepared through stage 2) is stable and can be stored as a solid in air at ambient temperature, for example, about 20°C. If necessary, they may be stored under inert conditions, for example, under nitrogen or argon, or at low temperatures, for example, in a refrigerator or freezer. Sometimes, the compound of formula I is stored in a solvent, for example, dissolved in ethanol. In some cases, the compound of formula I is stored in the solvent for 8 hours or more, typically 12 hours or more.

[0169] As noted above, the compound of formula I may be in the form of a pharmaceutically acceptable salt. A pharmaceutically acceptable salt can be formed from the compound of formula I by reaction with a suitable acid. Thus, the method can further include Stage 3, in which the compound of formula I is reacted with an acidic reagent to produce a pharmaceutically acceptable salt of the compound of formula I. The acidic reagent is suitable for crystallizing the pharmaceutically acceptable salt of the compound of formula I.

[0170] For the avoidance of doubt, when a reagent is expressed herein as a number of equivalents, this is relative to the molar equivalent of a compound of Formula III, Formula II or Formula I for the reagent in Stage 1, Stage 2 or Stage 3, respectively.

[0171] The method of synthesizing a compound of Formula I or a pharmaceutically acceptable salt thereof often includes Stage 1, Stage 2, and Stage 3, with Stage 1 comprising the following steps: (i) reacting a compound of formula III with two or more coupling agents to form an activated compound; (ii) reacting the activated compound with a compound of formula (R 2 ) with an amine having 2NH to produce a compound of formula II; (iii) isolating the compound of formula II. Stage 2 involves reacting a compound of formula II with LiAlD or LiAlH with LiAlD; Stage 3 involves reacting the compound of formula I with an acidic reagent suitable for crystallizing a pharmaceutically acceptable salt of the compound of formula I.

[0172] In some cases, a ratio of ≧1:1 acidic reagent to compound of Formula I is used. Often, the ratio of acidic reagent to compound of Formula I is 1:1.

[0173] Typically, Stage 3 of this method is carried out in a suitable solvent. Those skilled in the art will be able to assess which solvent is appropriate for this stage. Examples of suitable solvents include ethanol, IPA, iPrOAc, and MeCN. Stage 3 is often carried out in ethanol.

[0174] Stage 3 of the method of the present invention is carried out at a suitable temperature, and one skilled in the art will be able to assess which temperatures are suitable for these steps.

[0175] Stage 3 of this method often involves contacting a compound of Formula I with an acidic reagent to form a first composition. Often, the contacting in Stage 3 is carried out at a temperature of 70-100° C., e.g., 70-90° C. or 70-80° C. Sometimes, the contacting in Stage 3 is carried out at a temperature of about 75° C.

[0176] Often, Stage 3 further includes isolating the pharmaceutically acceptable salt of Formula I. Those skilled in the art are familiar with techniques suitable for isolating such compounds. For example, if the compound is dissolved in a suspension, it can be separated from some of the other components of the suspension by filtration, such as hot filtration. The pharmaceutically acceptable salt of Formula I may precipitate from the filtrate. Those skilled in the art are familiar with methods to promote precipitation of the compound from solution, such as cooling the solution, concentrating the solution, and / or adding a crystalline form of the compound to the solution to promote nucleation and further crystal growth (i.e., seeding). The pharmaceutically acceptable salt of Formula I may also be recrystallized. Those skilled in the art are familiar with techniques suitable for recrystallizing a pharmaceutically acceptable salt of Formula I. The example recrystallization techniques described for the recrystallization of a compound of Formula II apply, mutatis mutandis, to the recrystallization of a pharmaceutically acceptable salt of Formula I.

[0177] Stage 3 of the method may include the following steps: i. adding to a fifth vessel at least 1 equivalent of an acidic reagent suitable for crystallizing a pharmaceutically acceptable salt of the compound of Formula I; ii. dissolving the compound of formula I as a free base in 5-20 volumes of a solvent, such as a solvent selected from ethanol, IPA, iPrOAc, and MeCN, and adding this solution to a fifth reaction vessel; iii. stirring the contents of the fifth vessel at a temperature greater than 72°C (e.g., 72-90°C); iv. filtering the contents of the fifth vessel; v. adding the filtrate to a sixth vessel and cooling the contents to a temperature of 67°C to 73°C; vi. optionally, seeding a sixth vessel with a crystalline form of a pharmaceutically acceptable salt of the compound of Formula I; vii. stirring the contents of the sixth vessel at a temperature of 67°C to 73°C for at least 30 minutes (e.g., 30 minutes to 1 hour); viii. cooling the contents of the sixth vessel at a rate of 2°C to 8°C per hour to a temperature of -5°C to 5°C; ix. The contents of the sixth vessel are filtered to produce a filter-cake comprising a pharmaceutically acceptable salt of the compound of Formula I.

[0178] Often, the solvent in step ii is ethanol. Often, the cooling rate in step viii is 5°C per hour.

[0179] As noted above, pharmaceutically acceptable salts often comprise a compound of Formula I and a suitable acid. The acids listed above as suitable components of the pharmaceutically acceptable salts of the invention apply mutatis mutandis to the acidic reagent in Stage 3 of this process.

[0180] Often the acidic reagent is one selected from fumaric acid, tartaric acid, citric acid and hydrochloric acid, for example fumaric acid.

[0181] Examples of preferred hallucinogenic tryptamines that can be prepared by the above synthetic methods include those listed in Table 1. The R 1 and R 2 may be any of the combinations shown in Table 1. Also shown in Table 1 are the molecular weights of preferred drug substances, including mixtures of the compounds of Formula I and their protio and deuterated analogs.

[0182] [Table 1]

[0183] The synthetic method disclosed herein is particularly useful for producing therapeutic deuterated dialkyltryptamines because it substitutes deuterium at the α-position rather than the β-position, resulting in the use of significantly less LiAlD4 than other syntheses known in the art. LiAlD4 is the most expensive and difficult to prepare reagent in this synthesis. Furthermore, the optimized method disclosed herein reduces the required amount of LiAlD4 or LiAlH4 and LiAlD4, for example, from 2 equivalents to 0.9 equivalents, improving the economic efficiency of producing deuterated compounds of Formula I. In this regard, compounds of Formula I produced via the synthetic method disclosed herein are less expensive than known deuterated analogs, which are typically deuterated at both the α- and β-positions.

[0184] The synthetic methods disclosed herein are efficient and allow compounds of Formula I to be produced in overall yields of between 50% and 100%, for example, between 60% and 100%, or between 65% and 100%.

[0185] Also disclosed herein is a kit suitable for preparing a compound of Formula I, the kit including: (A) a compound of formula III, (B) two or more coupling agents; (C) Formula (R 2 ) amines having 2NH; (D) LiAlD4 or LiAlH4 and LiAlD4, and (E) an acidic reagent suitable for the preparation of pharmaceutically acceptable salts of compounds of formula I; wherein the compounds of formula I and III are as defined in relation to the synthetic methods disclosed herein.

[0186] For the avoidance of doubt, compounds of formula I and III, or pharmaceutically acceptable salts thereof, two or more coupling agents, 2 )NH, LiAlD or LiAlH and LiAlD, and the acidic reagents of the synthesis methods disclosed herein are applied mutatis mutandis to the kit. For example,2 ) 2NH amine R 2 (and thus the compound of formula I or a pharmaceutically acceptable salt thereof) may be methyl; R 1 may be methoxy or acetoxy, and / or n may be 1, R 1 may be at the 4- or 5-position; the two or more coupling agents may include a carbodiimide coupling agent and an additional coupling agent; the ratio of LiAlD4 or LiAlH4 and LiAlD4:compound of formula III may be 0.8:1 to 1:1, and / or the acidic reagent may be fumaric acid.

[0187] As noted above, the inventors have observed a quantifiable relationship between the degree of deuteration and the effect of enhancing the metabolic half-life of the parent compound. Viewed from a third aspect, there is provided a composition comprising at least a first and a second compound, or a pharmaceutically acceptable salt thereof, wherein the first compound is selected from the compounds defined in the first or second aspect, and the second compound is a non-deuterated analog of the first compound.

[0188] The first compound contains one or two deuterium atoms at the alpha position, but is identical to the second (non-deuterated, i.e., proteo) compound except for the presence of the one or two deuterium atoms.

[0189] Often, the composition comprises 2%, 5%, 10%, 15%, 20%, 25%, 30%, 50%, 60%, 75%, 90%, 95%, 96%, or 98% or more of the first compound by weight. In some embodiments, the composition comprises 2% and 90%, 2% and 95%, 2% and 96%, 2% and 97%, 2% and 98% by weight, e.g., 5% and 90%, 5% and 95%, 5% and 96%, 5% and 97%, 5% and 98%; 10% and 90%, 10% and 95%, 10% and 96%, 10% and 97%, 10% and 98%; 15% and 90%, 15% and 95%, 15% and 96%, 15% and 97%, or 15% and 98%. 20% and 90%, 20% and 95%, 20% and 96%, 20% and 97%, 20% and 98%; 25% and 90%, 25% and 95%, 25% and 96%, 25% and 97%, 25% and 98%; 30% and 90%, 30% and 95%, 30% and 96%, 30% and 97%, 30% and 98%; 50% and 90%, 50% and 95%, 50% and 96%, 50% and 97%, 50% and 98%; 60% and 90%, 60% and 95%, 60% and 96%, 60% and 97%, 60% and 98%; or between 75% and 90%, 75% and 95%, 75% and 96%, 75% and 97%, 75% and 98% of the first compound.

[0190] The composition may contain 2 to 98% by weight of the second compound, and preferably contains 5 to 95% by weight of the second compound. Preferred compositions contain 10 to 90% by weight of the second compound, 15 to 85% by weight of the second compound, 20 to 80% by weight of the second compound, 25 to 75% by weight of the second compound, 30 to 70% by weight of the second compound, or 40 to 60% by weight of the second compound.

[0191] The composition preferably contains 5 to 95% by weight of the first compound.

[0192] In some embodiments, the composition comprises a first compound, a second compound, and a third compound, wherein the first compound is selected from the compounds defined in the first aspect or the second aspect, with the proviso that: xH is protium, the second compound is a non-deuterated analog of the first compound, and the third compound is a deuterated analog of the first compound; x It differs from the first compound only in that H is deuterium rather than protium.

[0193] Typically, the composition comprises 2% or more by weight of the first or third compound. In some embodiments, the composition comprises 2% or more by weight of the first compound. In some embodiments, the composition comprises 2% or more by weight of the first compound and 2% or more by weight of the third compound.

[0194] It will be understood that when a composition comprises 2% or more by weight of a first or third compound, such a composition may comprise up to 95%, up to 96%, up to 97%, or up to 98% by weight of the first or third compound.

[0195] In some embodiments, the first compound comprises up to 50% by weight of the total composition, and in such embodiments, it will be understood that such compositions may comprise 2% or more by weight, such as 5% or more, 10% or more, 15% or more, 20% or more, 25% or more, or 30% or more of the first compound based on the total composition.

[0196] According to certain embodiments, the composition consists essentially of at least a first and a second compound, or a pharmaceutically acceptable salt thereof, wherein the first compound is selected from the compounds defined in the first or second aspect, and the second compound is a non-deuterated analog of the first compound. A composition consisting essentially of at least a first and a second compound means that the composition may contain additional components (other than at least the first and second compounds), but the presence of these additional components does not substantially affect the essential characteristics of the composition. In particular, a composition consisting essentially of at least a first and a second compound does not contain any substance amounts of other pharmaceutically active substances (i.e., substance amounts of other drug substances).

[0197] As described in detail in the Examples section and associated Figures 3 and 4, the inventors have demonstrated that increasing deuterium enrichment at the α-carbon of N,N-dimethyltryptamine increases metabolic stability, decreases clearance, and increases half-life. In particular, when the input reducing agent for producing deuterium-enriched N,N-dimethyltryptamine-containing compositions of the invention comprises LiAlH4 and LiAlD4 in a ratio of about 1:2.5 to about 2.5:1, a linear relationship exists between molecular weight and half-life.

[0198] According to certain embodiments, the composition of the third aspect comprises at least a first and a second compound, or a pharmaceutically acceptable salt thereof, wherein the first compound is selected from the compounds defined in the first or second aspect, and wherein R 1 and R 2 is as defined in Table 1, and the second compound is an undeuterated analog of the first compound. In some embodiments, the average molecular weight of the composition is as defined in Table 1.

[0199] In some embodiments, the composition comprises a first, second, and third compound, wherein the first compound is selected from the compounds defined in the first aspect or the second aspect, and wherein: x If H is protium, R 1 and R 2 is as defined in Table 1, the second compound is a non-deuterated analog of the first compound, and the third compound is a deuterated analog of the first compound; x The composition differs from the first compound only in that H is deuterium instead of protium. In some embodiments, the average molecular weight of the composition is as defined in Table 1.

[0200] In some embodiments, the composition of the third aspect consists essentially of the first, second, and optionally third compounds. As used herein, average molecular weight refers to the weighted average of the molecular weights of the first, second, and optionally third compounds, as measured by a suitable mass spectrometric technique, such as LC-MS SIM (selected ion monitoring), where applicable, ignoring the weight contribution due to the formation of pharmaceutically acceptable salts. In some embodiments, the average molecular weight is a weighted average.

[0201] It will be appreciated that providing a composition having such a specific average molecular weight in the reduction described herein, particularly by adjusting the relative ratios of lithium aluminum hydride and lithium aluminum deuteride, can be accomplished by one skilled in the art through the teachings herein.

[0202] By "the composition consists essentially of the first, second, and optionally third compounds," it is meant that the composition may contain additional components, but the presence of such additional components does not materially affect the essential characteristics of the composition. In particular, the composition does not contain material amounts of other pharmaceutically active compounds, including other compounds of Formula I and / or their proteomic analogs.

[0203] In other words, compositions according to these particular embodiments comprise a drug substance containing a biologically active component consisting essentially of a mixture of first, second and optionally third compounds, wherein the drug substance is optionally in the form of a pharmaceutically acceptable salt.

[0204] It will be understood that the compositions according to these particular embodiments contain a greater amount of the first and optionally third compounds than would be found in a non-isotopically enriched protio analog. It will also be understood that the greater the proportion of the first and optional third compounds in these particular embodiments, the higher the average molecular weight of the composition.

[0205] Viewed from a fourth aspect, there is provided a pharmaceutical composition comprising a compound as defined in the first aspect or a compound of the second aspect, or a pharmaceutically acceptable salt thereof, or a composition of the third aspect in combination with a pharmaceutically acceptable excipient.

[0206] The pharmaceutical compositions of the present invention can contain one or more pharmaceutically acceptable excipients. Suitable pharmaceutical compositions can be prepared by those skilled in the art using examples of pharmaceutically acceptable excipients, including but not limited to those listed in Gennaro et al., Remmington: The Science and Practice of Pharmacy, 20th Edition, Lippincott, Williams and Wilkins, 2000 (specifically, Part 5: Pharmaceutical Manufacturing). Suitable excipients are also listed in Handbook of Pharmaceutical Excipients, 2nd Edition; Editors A. Wade and PJ Weller, American Pharmaceutical Association, Washington, The Pharmaceutical Press, London, 1994. M.F. Powell, T. Nguyen and L. Baloian provide a review of excipients suitable for parenteral administration (administration other than via the mouth or digestive tract) in PDA J. Pharm. Sci. Technol., 52, 238-311 (1998). All soluble excipients listed in this review article are suitable excipients for use in the fourth aspect of the invention, including compositions suitable for oral, nasal, topical (including buccal, sublingual and transdermal), parenteral (including subcutaneous, intravenous and intramuscular) or rectal administration.

[0207] The pharmaceutical composition of the present invention can be compressed into solid dosage units such as tablets, or can be processed into capsules or suppositories.By using pharmaceutically suitable liquid, the compound can also be prepared in the form of solution, suspension, emulsion or spray.For the manufacture of dosage units including tablets, conventional additives such as fillers, colorants, polymer binders, etc. can be used.Generally, any pharmaceutically acceptable additives can be used.

[0208] Suitable fillers for preparing and administering pharmaceutical compositions include lactose, starch, cellulose, and derivatives thereof, etc., or mixtures thereof used in appropriate amounts. For parenteral administration, aqueous suspensions, isotonic saline solutions, and sterile injection solutions can be used, which contain pharmaceutically acceptable dispersants and / or wetting agents, such as propylene glycol or butylene glycol.

[0209] The present invention also provides a packaging material containing instructions for use of the pharmaceutical composition in combination with the pharmaceutical composition of the present invention and suitable packaging material for the composition.

[0210] As noted above, the compounds and compositions of the invention have use in the treatment of psychiatric or neurological disorders. Viewed from a fifth aspect, therefore, there is provided a composition of the third or fourth aspect for use in therapy.

[0211] In some embodiments, the treatment is hallucinogenic-assisted psychotherapy, i.e., the treatment is the treatment of a mental illness by hallucinogenic means, which is augmented by one or more protocols in which the patient undergoes a hallucinogenic experience induced by administration of a compound or composition.

[0212] Viewed from a sixth aspect, there is provided a compound as defined in the first or second aspect, a pharmaceutically acceptable salt thereof, or a composition of the third or fourth aspect, for use in a method of treating a psychiatric or neurological disorder in a patient.

[0213] In another aspect, the invention provides the use of a compound defined in the first or second aspect, a pharmaceutically acceptable salt thereof, or a composition of the third or fourth aspect, for the manufacture of a medicament, in some embodiments, the medicament for use in a method of treating a psychiatric or neurological disorder in a patient.

[0214] In some embodiments, the psychiatric or neurological disorder is selected from (i) obsessive-compulsive disorder, (ii) depressive disorder, (iii) schizophrenia, (iv) schizophrenia-type disorder, (v) anxiety disorder, (vi) substance abuse, and (vii) anorexia. Often, the psychiatric or neurological disorder is selected from the group consisting of (i) obsessive-compulsive disorder, (ii) depressive disorder, (iii) anxiety disorder, (iv) substance abuse, and (v) anorexia.

[0215] In some embodiments, the disorder is selected from the group consisting of major depressive disorder, treatment-resistant major depressive disorder, postpartum depression, and eating disorders such as obsessive-compulsive disorder and compulsive eating disorder.

[0216] In some embodiments, the psychiatric or neurological disorder is major depressive disorder. In some embodiments, the psychiatric or neurological disorder is treatment-resistant depression.

[0217] As noted above, the compounds of the present invention have improved oral bioavailability because their metabolism by monoamine oxidase enzymes in the gastrointestinal tract is slower than their α-diploid analogs. Thus, in some embodiments, treatment or methods of treatment involve oral administration of the compound, pharmaceutically acceptable salts thereof, or compositions thereof.

[0218] Viewed from a seventh aspect, there is provided a method of treatment comprising administering to a patient in need thereof a compound as defined in the first or second aspect, a pharmaceutically acceptable salt thereof, or a composition of the third or fourth aspect.

[0219] In some embodiments, the method of treatment is hallucinogenically assisted psychotherapy, i.e., the method of treatment is the treatment of a psychiatric disorder by hallucinogenic means augmented by one or more protocols in which the patient undergoes a hallucinogenic experience induced by the administration of a compound or composition.

[0220] In some embodiments, the method of treatment is a method of treating a psychiatric or neurological disorder. For the avoidance of doubt, embodiments relating to the method of treatment of the fifth or sixth aspects of the present invention apply mutatis mutandis to the seventh aspect. For example, the disorder may be selected from the group consisting of (i) obsessive-compulsive disorder, (ii) depressive disorder, (iii) anxiety disorder, (iv) substance abuse, and (v) anorexia disorder; and / or the method of treatment may comprise oral administration of a compound or composition.

[0221] To treat the aforementioned diseases, an effective amount of the compound, pharmaceutically acceptable salt or composition is administered, i.e., an amount sufficient to reduce or halt the rate of progression of the disease, or to ameliorate or treat the disease and produce the desired therapeutic or suppressive effect.

[0222] As described above, the compounds of the present invention have improved oral bioavailability. Accordingly, in view of an eighth aspect, there is provided an oral dosage form comprising a compound defined in the first or second aspect, a pharmaceutically acceptable salt thereof, or a composition according to the third or fourth aspect. "Oral dosage form" refers to a specific form (e.g., a tablet or capsule) containing a specific dose of a compound or composition, which form is suitable for oral administration. The oral dosage form may be a solid dosage form such as a tablet, capsule, sachet, powder, or granule, or a liquid or semi-solid oral dosage form such as a syrup, solution, ampule, or dispersion. Typically, the oral dosage form is a solid dosage form, often a tablet or capsule.

[0223] Each and every reference referred to herein is incorporated herein by reference in its entirety, as if the entire contents of each reference were set forth herein in its entirety.

[0224] The present invention can be further understood with reference to the following non-limiting clauses and examples.

[0225] 1. A compound of formula I or a pharmaceutically acceptable salt thereof. [ka] In this case, at least one x H is deuterium and R 1 is R 3 , OR 3 , (O(CO)R 3 , F, Cl, Br, or I, and each R 2 and R 3 are each independently selected from C1-C4 alkyl.

[0226] 2. R 1 OR 3 , preferably OMe.

[0227] 3. Each R 2 3. The compound of clause 1 or 2, wherein is methyl.

[0228] 4. Both x 4. The compound of any of clauses 1 to 3, wherein H is deuterium.

[0229] 5. A method for synthesizing a compound of formula I or a pharmaceutically acceptable salt thereof, comprising two stages, wherein stage 1 comprises reacting a compound of formula III with a combination of two or more coupling agents, followed by reaction with a compound of formula (R 2 ) 2NH with an amine, and Stage 2 comprises reacting a compound of Formula II with LiAl x reducing with H4, [ka] At this time, LiAl x H4 is LiAlD4, optionally containing 0.1 to 99.9% LiAlH4; Each R1 are independently 3 , OR 3 , 0(CO)R 3 , F, Cl, Br or I, and Each R 2 and R 3 is independently selected from C1-C4 alkyl.

[0230] 6. The method of clause 5, wherein the compound of formula I is a pharmaceutically acceptable salt, the method consisting essentially of three stages, stage 1 comprising the steps of: i. reacting a compound of formula III with a combination of two or more coupling agents; ii. The obtained intermediate is reacted with a compound of formula (R 2 ) reacting with an amine having 2NH, iii. isolating the compound of formula II, Stage 2 involves reacting the compound of formula II with LiAl x H4 reduction step, Stage 3 involves reacting the compound of formula I with an acidic reagent suitable for crystallizing a pharmaceutically acceptable salt of the compound of formula I.

[0231] 7. The method of clause 5 or 6, wherein Stage 1 comprises the steps of: iv. adding 1 g or more of a compound of Formula III and 1 to 1.5 equivalents of an additional coupling agent to a first vessel; v.DCM, acetone, IPA, i adding 5 to 20 volumes of a first solvent selected from PrOAc, TBME, 2-MeTHF, and EtOAc to a first vessel; vi. adding 1 to 1.5 equivalents of a carbodiimide coupling agent to the first vessel; vii. stirring the contents of the first container for at least 30 minutes, preferably at least 1 hour, between 10°C and 30°C; viii. Formula (R 2 ) adding 1 to 2 equivalents of an amine having a 2NH group to a first vessel, wherein the amine is preferably dissolved in an ether solvent; ix. further stirring the contents of the first container for at least 30 minutes, preferably at least 1 hour, at 10°C to 30°C; x. Add 2 to 10 volumes of an aqueous basic solution, preferably 10% potassium carbonate, to a first container; xi. further stirring the contents of the first container for at least 1 minute, preferably at least 5 minutes, between 10°C and 30°C; xii. separating an organic fraction from the aqueous fraction, wherein the organic fraction comprises a compound of formula II; xiii. removing the organic fraction containing the compound of formula II; In this case, steps iv to xiii are carried out within a single 8 hour period.

[0232] 8. The method of any of clauses 5-7, wherein the two or more coupling agents comprise EDC, preferably as the HCl salt.

[0233] 9. The method of any of clauses 5-8, wherein the two or more coupling agents include an additional coupling agent selected from HOBt, HOOBt, HOSu, HOAt, ethyl 2-cyano-2-(hydroxymino)acetate, and DMAP.

[0234] 10. The method of any of clauses 5-9, wherein the two or more coupling agents include carbodiimide EDC.HCl and an additive coupling agent HOBt.

[0235] 11. The method of any of clauses 5 to 10, wherein the reaction in Stage 1 is carried out in DCM as the solvent.

[0236] 12. The method of any of clauses 5-11, wherein the amine is 2M dimethylamine in THF.

[0237] 13. The method of any of clauses 5 to 12, wherein Stage 1 further comprises the steps of: xiv. drying the organic fraction with a drying agent selected from calcium chloride, magnesium sulfate, and sodium sulfate; xv. Filtration of the organic fraction; xvi. Concentrating the organic fraction under a pressure of less than 1 atmosphere; xvii. adding the concentrated organic fraction to a second vessel; xviii. adding 2-10 volumes of a second solvent to a second vessel, wherein the second solvent is selected from IPA, EtOAc, iPrOAc, MeCN, TBME, THF, 2-MeTHF, and toluene; xix. Stirring the contents of the second vessel for at least 1 hour, preferably at least 2 hours, between 45°C and 55°C; xx. Cooling the contents of the second container to between 15°C and 25°C; xxi. filtering the contents of the second vessel to obtain a filtrate, wherein the filtrate comprises a compound of Formula II; xxii. Dry the filtrate.

[0238] 14. The method of clause 13, wherein the second solvent is selected from TBME and IPA.

[0239] 15. The method of any of clauses 5 to 14, wherein Stage 2 comprises the steps of: xxiii. adding 1 g or more of a compound of formula II to a third container; xxiv. Adding between 5 and 20 volumes of ether solvent to a third vessel; xxv. Add LiAl in ethereal solvent to a third vessel over a period of at least 15 minutes. x 0.8 to 1 equivalent of H4, preferably a 2M solution in THF, is added dropwise while maintaining the temperature of the third vessel between -5°C and 65°C; xxvi. Stirring the contents of the third vessel between 55°C and 65°C for 1 hour to 6 hours, preferably 2 hours; xxvii. cooling the contents of the third vessel to between 10°C and 30°C; The contents of the third container then comprise the compound of Formula I.

[0240] 16. The method of any of clauses 5 to 15, wherein Stage 2 includes a workup comprising the steps of: xxviii. Adding 5 to 20 volumes of an aqueous tartrate solution to a fourth container; xxix. adding a composition comprising the crude compound of formula III to a fourth vessel at between 15°C and 25°C for at least 15 minutes, preferably at least 30 minutes; xxx. Stir the contents of the fourth vessel between 15°C and 25°C for at least 30 minutes.

[0241] 17. The method of clause 16, wherein stage 2 further comprises the steps of: xxxi. separating an organic fraction from the aqueous fraction, wherein the organic fraction comprises a compound of formula I; xxxii. removing the aqueous fraction from the fourth vessel; xxxiii. adding 5 to 20 volumes of brine solution to a fourth container; xxxiv. stirring the contents of the fourth vessel at a temperature between 15°C and 25°C for at least 5 minutes; xxxv. Removing the organic fraction containing the compound of formula I as a free base; xxxvi. drying the organic fraction using a drying agent selected from calcium chloride, magnesium sulfate, and sodium sulfate; xxxvii. filtering the organic fraction; xxxviii. Concentrating the organic fraction under a pressure of less than 1 atmosphere.

[0242] 18. Any of the methods of clauses 5 to 17, wherein stage 3 comprises the steps of: xxxix. adding to a fifth vessel at least one equivalent of an acidic reagent suitable for crystallizing a pharmaceutically acceptable salt of the compound of Formula I; x1.1 g or more of the compound of formula I as free base, in ethanol, IPA, i Dissolving in 5 to 20 equivalents of a solvent selected from PrOAc and MeCN, and adding the solution to a fifth reaction vessel; xli. stirring the contents of the fifth vessel at a temperature of at least 72°C; xlii. filtering the contents of the fifth vessel; xliii. adding the filtrate to a sixth vessel and cooling the contents to a temperature of 67°C to 73°C; xliv. optionally, seeding a sixth vessel with a crystalline form of a pharmaceutically acceptable salt of the compound of Formula I; xlv. stirring the contents of the sixth vessel at a temperature of 67°C to 73°C for at least 30 minutes; xlvi. cooling the contents of the sixth vessel at a rate of 2 to 8°C per hour to a temperature of -5°C to 5°C; xlvii. Filtering the contents of the sixth vessel to produce a filter cake comprising a pharmaceutically acceptable salt of the compound of Formula I.

[0243] 19. The method of any of clauses 5-18, wherein the compound of formula I or a pharmaceutically acceptable salt thereof is produced in greater than 99% purity by HPLC.

[0244] 20. A compound according to any one of clauses 1 to 4, obtainable by the method according to any one of clauses 5 to 19.

[0245] 21. A compound according to any of clauses 1 to 4 and 20 for use in psychedelic-assisted psychotherapy.

[0246] 22. A compound according to any of clauses 1 to 4 for use in the treatment of a mental or psychotic disorder selected from (i) obsessive-compulsive disorder, (ii) depressive disorder, (iii) schizophrenia, (iv) schizophrenia-type disorder, (v) anxiety disorder, (vi) substance abuse, and (vii) anorexia disorder.

[0247] 23. A kit for synthesizing a compound of formula I, the kit comprising: a. A compound of formula III, b. two or more coupling agents; c.Formula (R 2 ) amines having 2NH; d.LiAl x H4, and optionally, e. An acidic reagent suitable for crystallizing a pharmaceutically acceptable salt of a compound of Formula I Including, [ka] In the above formula, LiAl x H4 is LiAlH4, LiAlD4 or a mixture thereof; Each R 1 are independently 3 , OR 3 , 0(CO)R 3 , F, Cl, Br or I, and Each R 2 and R 3 is independently selected from C1-C4 alkyl.

[0248] 24. An oral dosage form comprising a compound according to any one of clauses 1 to 4 and 21 to 24.

[0249] 25. The compound, method, kit, or oral dosage form of any preceding claim, wherein the compound of formula I is selected from α-deutero-5-methoxydimethyltryptamine, α,α-dideutero-5-methoxydimethyltryptamine, or a mixture thereof.

[0250] 26. A method for synthesizing a compound of formula III or a pharmaceutically acceptable salt thereof, comprising two stages, wherein stage 1 comprises reacting a compound of formula I with a combination of two or more coupling agents, followed by reaction with a compound of formula (R 2 ) 2NH with an amine, and Stage 2 comprises reacting a compound of Formula II with LiAl x reducing with H4, [ka] In the above formula, each x H is independently selected from protium and deuterium; n is selected from 0, 1, 2, 3 or 4; Each R 1 are independently 3 , -OR 3 , -O(CO)R 3 , F, Cl, Br or I, and Each R 2 and R 3is independently selected from C1-C4 alkyl.

[0251] 27. The method of clause 26, wherein Stage 1 further comprises isolating the compound of formula II.

[0252] 28. The method of clause 26, wherein the compound of formula III is a pharmaceutically acceptable salt, said method consisting essentially of three stages: Stage 1 involves the following steps: i. reacting a compound of formula I with a combination of two or more coupling agents; ii. The obtained intermediate is reacted with a compound of formula (R 2 ) reacting with an amine having 2NH, iii. isolating the compound of formula II, Stage 2 involves reacting the compound of formula II with LiAl x reducing the compound with H4; Stage 3 involves reacting the compound of formula III with an acidic reagent suitable for crystallizing a pharmaceutically acceptable salt of the compound of formula III.

[0253] 29. Any of the methods of clauses 26 to 31, wherein stage 1 comprises the steps of: i. adding to a first container at least 1 g of a compound of Formula I and 1 to 1.5 equivalents of an additional coupling agent; ii. DCM, acetone, IPA, i adding 5-20 volumes of a first solvent selected from PrOAc, TBME, 2-MeTHF, and EtOAc to a first vessel; iii. adding 1 to 1.5 equivalents of a carbodiimide coupling agent to a first vessel; iv. stirring the contents of the first container for at least 30 minutes, preferably at least 1 hour, at a temperature between 10°C and 30°C; v.Formula(R 2 ) Between 1 and 2 equivalents of an amine having 2NH is added to a first vessel, wherein the amine is preferably dissolved in an ether solvent; vi. further stirring the contents of the first container for at least 30 minutes, preferably at least 1 hour, between 10°C and 30°C; vii. adding 2-10 volumes of an aqueous basic solution, preferably 10% potassium carbonate, to a first container; viii. further stirring the contents of the first container for at least 1 minute, preferably at least 5 minutes, between 10°C and 30°C; ix. separating an organic fraction from the aqueous fraction, wherein the organic fraction comprises a compound of formula II; x. removing the organic fraction containing the compound of formula II; In this case, steps i. to x. are carried out within a single 8 hour period.

[0254] 30. The method of any of clauses 26-29, wherein the two or more coupling agents include EDC, preferably as the HCl salt.

[0255] 31. The process of any of clauses 26-30, wherein the two or more coupling agents include an additional coupling agent selected from HOBt, HOOBt, HOSu, HOAt, ethyl 2-cyano-2-(hydroxymino)acetate, and DMAP.

[0256] 32. The method of any of clauses 26-31, wherein the two or more coupling agents include carbodiimide EDC.HCl and an additive coupling agent HOBt.

[0257] 33. The method of any of clauses 26 to 32, wherein the reaction in Stage 1 is carried out in DCM as a solvent.

[0258] 34. The process of any of clauses 26-33, wherein the amine is 2M dimethylamine in THF.

[0259] 35. The method of any of clauses 28 to 34, wherein stage 1 further comprises the steps of: xi. drying the organic fraction with a drying agent selected from calcium chloride, magnesium sulfate, and sodium sulfate; xii. Filtration of the organic fraction; xiii. concentrating the organic fraction under a pressure of less than 1 atmosphere; xiv. adding the concentrated organic fraction to a second container; xv. Add 2-10 volumes of a second solvent to a second container, where the second solvent is IPA, EtOAc, i selected from ProAc, MeCN, TBME, THF, 2-MeTHF and toluene; xvi. Stirring the contents of the second vessel for at least 1 hour, preferably at least 2 hours, between 45°C and 55°C; xvii. cooling the contents of the second vessel to between 15°C and 25°C; xviii. filtering the contents of the second vessel to obtain a filtrate, wherein the filtrate comprises a compound of Formula II; xix. The filtrate is dried.

[0260] 36. The method of clause 35, wherein the second solvent is selected from TBME and IPA.

[0261] 37. The method of any of clauses 26 to 36, wherein stage 2 further comprises the steps of: i. adding 1 g or more of a compound of Formula II to a third container; ii. adding between 5 and 20 volumes of ether solvent to a third vessel; iii. Add LiAl in ether solvent to a third vessel over a period of at least 15 minutes. x 0.8 to 1 equivalent of H4, preferably a 2M solution in THF, is added dropwise while maintaining the temperature of the third vessel between -5°C and 65°C; iv. stirring the contents of the third vessel at between 55°C and 65°C for 1 hour to 6 hours, preferably 2 hours; and v. cooling the contents of the third container to between 10°C and 30°C; The contents of the third container then comprise a compound of formula III.

[0262] 38. The method of any of clauses 26 to 37, wherein stage 2 includes post-processing including the steps of: vi. Adding 5 to 20 volumes of an aqueous tartrate solution to a fourth container; vii. adding a composition comprising the crude compound of formula III to a fourth vessel at between 15°C and 25°C for at least 15 minutes, preferably at least 30 minutes; viii. Stir the contents of the fourth vessel between 15°C and 25°C for at least 30 minutes.

[0263] 39. The method of clause 38, wherein stage 2 further comprises the steps of: ix. separating an organic fraction from the aqueous fraction, wherein the organic fraction comprises a compound of formula III; x. removing the aqueous fraction from the fourth vessel; xi. Add 5 to 20 volumes of brine solution to a fourth container; xii. stirring the contents of the fourth vessel at a temperature between 15°C and 25°C for at least 5 minutes; xiii. removing the organic fraction containing the compound of formula III as a free base; xiv. drying the organic fraction with a drying agent selected from calcium chloride, magnesium sulfate, and sodium sulfate; xv. filtering the organic fraction, and xvi. Concentrate the organic fraction under a pressure of less than 1 atmosphere.

[0264] 40. The method of any of clauses 26 to 39, wherein stage 3 comprises the steps of: i. adding at least one equivalent of an acidic reagent suitable for crystallizing a pharmaceutically acceptable salt of a compound of Formula III to a fifth vessel; ii. Dissolve 1 g or more of the compound of formula III as a free base in ethanol, IPA, i Dissolving in 5 to 20 equivalents of a solvent selected from ProAc and MeCN, and adding this solution to a fifth reaction vessel; iii. stirring the contents of the fifth vessel at a temperature of at least 72°C; iv. filtering the contents of the fifth vessel; v. adding the filtrate to a sixth vessel and cooling the contents to a temperature of 67°C to 73°C; vi. optionally, seeding a sixth vessel with a crystalline form of a pharmaceutically acceptable salt of the compound of Formula III; vii. stirring the contents of the sixth vessel at a temperature of 67°C to 73°C for at least 30 minutes; viii. cooling the contents of the sixth vessel at a rate of 2 to 8°C per hour to a temperature of -5°C to 5°C; ix. Filtering the contents of the sixth vessel to produce a filter cake comprising a pharmaceutically acceptable salt of the compound of Formula III.

[0265] 41. The process of any of clauses 26-40, wherein the compound of formula III is obtained in an overall yield of 50% or greater.

[0266] 42. The method of any of clauses 26-41, wherein the compound of formula III is produced in an overall yield of 65% or greater.

[0267] 43. The method of any of clauses 26-42, wherein the compound of formula III or a pharmaceutically acceptable salt thereof is produced in a purity of greater than 99% by HPLC.

[0268] 44. A composition comprising a compound of formula III or a pharmaceutically acceptable salt thereof, in a purity greater than 99.9% by HPLC.

[0269] 45. The composition of clause 44, wherein the compound of formula III or a pharmaceutical salt thereof is present in a purity of 99.95% or greater by HPLC.

[0270] 46. ​​The composition of either clause 44 or 45, having no more than two impurity peaks by HPLC and no more than 0.2% impurity peaks by HPLC.

[0271] 47. A composition according to any one of clauses 44 to 46 obtained by the method according to any one of clauses 26 to 43.

[0272] 48. n is 0 or n is 1 and R 1 48. The method of any of clauses 26-43 or the composition of any of clauses 44-47, wherein is selected from 4-methoxy, 5-methoxy, 4-acetoxy, and 5-acetoxy.

[0273] 49 each R 2 49. The method of any of clauses 26-43 or 48 or the composition of any of clauses 44-48, wherein is methyl.

[0274] 50. A composition according to any of clauses 44 to 49 for use in hallucinogenic-assisted psychotherapy.

[0275] 51. The composition of any of clauses 44 to 50 for use in treating a mental or psychotic disorder selected from (i) obsessive-compulsive disorder, (ii) depressive disorder, (iii) schizophrenia, (iv) schizophrenia-type disorder, (v) anxiety disorder, (vi) substance abuse, and (vii) anmotivation disorder.

[0276] 52. The composition of any of clauses 44-51, wherein the compound of formula III is DMT or 5-MeO-DMT.

[0277] 53. The composition of any of clauses 44-52, wherein the pharmaceutically acceptable salt of the compound of formula III is DMT fumarate, preferably crystalline having a pattern A polymorphic form.

[0278] 54. A composition according to any one of clauses 44 to 53 for use as an antidepressant.

[0279] 55. A kit for synthesizing a compound of formula III, the kit comprising: b. A compound of formula I, c. two or more coupling agents; d.Formula R 2 amines having 2NH, e.LiAl x H4, and f. An acidic reagent suitable for crystallizing a pharmaceutically acceptable salt of a compound of Formula III [ka] In the above formula, each x H is independently selected from protium and deuterium; n is selected from 0, 1, 2, 3 or 4; Each R 1 are independently 3 , -OR 3 , -O(CO)R 3 , F, Cl, Br or I, and Each R 2 and R 3 is independently selected from C1-C4 alkyl. [Example]

[0280] 220.9 g of N,N-DMT (as free base) was prepared as N,N-DMT fumarate using the formula shown in Scheme 2. Another 4-6 g of the six partially deuterated mixtures were also prepared using modified conditions.

[0281] [ka]

[0282] DMT Stage 1: Coupling of indole-3-acetic acid with dimethylamine In a 5 L vessel under N2, indole-3-acetic acid (257.0 g, 1.467 mol), HOBt (~20% wet) (297.3 g, 1.760 mol), and DCM (2313 mL) were added to give a milky white suspension. EDC.HCl (337.5 g, 1.760 mol) was then added dropwise over 5 min at 16-22 °C. The reaction mixture was stirred at ambient temperature for 2 h before adding 2 M dimethylamine in THF (1100 mL, 2.200 mol) dropwise over 20 min at 20-30 °C. The resulting solution was stirred at ambient temperature for 1 h, where HPLC showed 1.1% indole-3-acetic acid and 98.1% stage 1. The reaction mixture was then charged with 10% K2CO3 (1285 mL) and stirred for 5 min. The layers were separated, and the upper aqueous layer was extracted with DCM (643 mL x 2). The organic extracts were combined and washed with saturated brine (643 mL). The organic extract was then dried over MgSO, filtered, and concentrated under reduced pressure at 45° C. This gave 303.1 g of crude Stage 1 as an off-white sticky solid. The crude material was then slurried in TBME (2570 mL) at 50° C. for 2 hours before being cooled to ambient temperature, filtered, and washed with TBME (514 mL×2). The filter cake was then dried in vacuo at 50° C. to give 266.2 g (yield=90%) of Stage 1 as an off-white solid with a purity of 98.5% by HPLC and >95% by NMR.

[0283] Stage 2: Preparation of DMT A 5 L vessel under N2 was charged with Stage 1 (272.5 g, 1.347 mol) and THF (1363 mL), resulting in an off-white suspension. Next, 2.4 M LiAlH4 in THF (505.3 mL, 1.213 mol) was added dropwise over 35 min at 20-56 °C to give an amber solution. This solution was heated to 60 °C for 2 h, where HPLC showed Stage 1 ND, Stage 2 92.5%, Imp 1 2.6%, and Imp 2 1.9%. The completed mixture was cooled to ambient temperature and then added dropwise over 30 min to a 25% solution of Rochelle's salt (aqueous) (2725 mL) at 20-30 °C. The resulting milky suspension was stirred at 20-25 °C for 1 h, after which the layers were separated and the upper organic layer was washed with saturated brine (681 mL). The organic layer was then dried over MgSO, filtered, and concentrated under reduced pressure at 45° C. The resulting crude oil was azeotroped with EtOH (545 mL×2) to give 234.6 g (yield=92%) of Stage 2 with a purity of 95.0% by HPLC and >95% by NMR.

[0284] Stage 3a (i)-(iii): Preparation of seed crystals of DMT fumarate (i) Stage 2 (100 mg) was taken up in 8 volumes of isopropyl acetate and warmed to 50°C before being charged with fumaric acid (1 equivalent) as a solution in ethanol. The flask was then aged at 50°C for 1 hour before being cooled to room temperature and stirred overnight to give a white suspension. The solid was isolated by filtration and dried at 50°C for 4 hours to give 161 mg of product (>99% yield). Purity was 99.5% by HPLC and >95% by NMR. (ii) Replacing isopropyl acetate with isopropyl alcohol in method (i) gave a white suspension after stirring overnight. The solid was isolated by filtration and dried at 50°C for 4 hours to give 168 mg of product (>99% yield). Purity was determined to be 99.8% by HPLC and >95% by NMR. Substituting tetrahydrofuran for isopropyl acetate in method (i) gave a white suspension after stirring overnight. The solid was isolated by filtration and dried at 50°C for 4 hours to give 161 mg of product (>99% yield). Purity was determined to be 99.4% by HPLC and >95% by NMR. Analysis by x-ray powder diffraction showed that the products of each of Methods 9i)-(iii) were identical to those labeled Pattern A.

[0285] Stage 3b: Preparation of DMT fumarate A 5 L flange flask under N2 was charged with fumaric acid (152.7 g, 1.315 mol) and Stage 2 (248.2 g, 1.315 mol) as a solution in ethanol (2928 mL). The mixture was heated to 75 °C, resulting in a dark brown solution. The solution was polish filtered into a preheated (80 °C) 5 L jacketed vessel. The solution was then cooled to 70 °C and seeded with Pattern A (0.1 wt%). The seeds were allowed to mature for 30 min each before being cooled to 0 °C at a rate of 5 °C / hr. After stirring at 0 °C for an additional 4 h, the batch was filtered, washed with cold ethanol (496 mL x 2), and then dried overnight at 50 °C. This afforded 312.4 g (yield = 78%) of Stage 3 with a purity of 99.9% by HPLC and >95% by NMR. XRPD: Pattern A.

[0286] 5MeO-DMT Stage 1: Coupling of 5-methoxyindole-3-acetic acid with dimethylamine A 100 mL three-neck flask under N2 was charged with 5-methoxyindole-3-acetic acid (3.978 g, 19.385 mmol), HOBt (~20% wet) (3.927 g, 23.261 mmol), and DCM (40 mL). EDC.HCl (4.459 g, 23.261 mmol) was then added dropwise over 15 minutes at <30 °C. The reaction mixture was stirred at ambient temperature for 1 hour, after which 2 M dimethylamine (14.54 mL, 29.078 mmol) was added dropwise over 15 minutes at <25 °C. After stirring for 1 hour, HPLC showed no starting material (SM, i.e., 5-methoxyindole-3-acetic acid) remained. The reaction mixture was then charged with 10% K2CO3 (20 mL), stirred for 5 minutes, and then separated. The lower aqueous layer was removed and back-extracted with DCM (10 mL x 2). The organic extracts were combined, washed with saturated brine (10 mL), dried over MgSO4, and filtered. The filtrate was concentrated in vacuo at 45 °C to give 3.898 g of active product (yield = 87%) with a purity of 95.7% by HPLC.

[0287] Stage 2: Preparation of 5MeO-DMT A 100 mL three-neck flask under N2 was charged with the stage 1 methoxy derivative (3.85 g, 16.586 mmol) and THF (19.25 mL). 2.4 M LiAlH4 (6.22 mL, 14.927 mmol) in THF was then added dropwise over 30 min at <40 °C. The reaction mixture was heated to 60 °C for 1 h, at which point HPLC indicated that 0.1% SM (stage 1 methoxy derivative) remained. The reaction mixture was then cooled to ambient temperature and quenched into 25% Rochelle's salt (38.5 mL) over 30 min at <30 °C. The resulting suspension was stirred for 1 h before being allowed to separate. The lower aqueous layer was then removed, and the upper organic layer was washed with saturated brine (9.6 mL). The organics were then dried over MgSO4, filtered, and concentrated in vacuo before azeotroping with EtOH (10 mL x 2). This gave 3.167 g of active (yield=88%) product with a purity of 91.5% by HPLC.

[0288] Stage 3: Preparation of 5MeO-DMT fumarate A 50 mL three-neck flask under N2 was charged with fumaric acid (1.675 g, 14.430 mmol) and a solution of the stage 2 methoxy derivative (3.15 g, 14.430 mmol) in EtOH (37.8 mL). The mixture was then heated to 75 °C for 1 h, but this did not produce a solution as expected. The mixture was further heated to reflux (78 °C), but still no solution was obtained. Therefore, the suspension was cooled to 0-5 °C, filtered, washed with EtOH (8 mL × 2), and then dried at 50 °C overnight. This gave 3.165 g of material (yield = 65%) with a purity of 99.9% by HPLC.

[0289] α,α-Dideutero-5-methoxydimethyltryptamine For Stage 1 (coupling of 5-methoxyindole-3-acetic acid with dimethylamine), see above.

[0290] Stage 2: Preparation of α,α-dideutero-5-methoxydimethyltryptamine A 100 mL three-neck flask under N2 was charged with the stage 1 methoxy derivative (3.85 g, 16.586 mmol) and THF (19.25 mL). 2.4 M LiAlD4 in THF (6.22 mL, 14.927 mmol) was then added dropwise over 30 min at <40 °C. The reaction mixture was heated to 60 °C for 1 h, at which point HPLC indicated that 0.1% SM (stage 1 methoxy derivative) remained. The reaction mixture was then cooled to ambient temperature and quenched into 25% Rochelle's salt (38.5 mL) over 30 min at <30 °C. The resulting suspension was stirred for 1 h and then separated. The lower aqueous layer was then removed, and the upper organic layer was washed with saturated brine (9.6 mL). The organics were then dried over MgSO4, filtered, and concentrated in vacuo to obtain an azeotrope from EtOH (10 mL × 2). This gave 3.196 g of active (yield=88%) product with a purity of 91.5% by HPLC.

[0291] Stage 3: Preparation of α,α-dideutero-5-methoxydimethyltryptamine fumarate A 50 mL three-neck flask under N2 was charged with fumaric acid (1.675 g, 14.430 mmol) and a solution of the stage 2 methoxy derivative (3.15 g, 14.430 mmol) in EtOH (37.8 mL). The mixture was then heated to 75 °C for 1 h, but this did not produce a solution as expected. The mixture was further heated to reflux (78 °C), but still no solution was obtained. Therefore, the suspension was cooled to 0-5 °C, filtered, washed with EtOH (8 mL × 2), and then dried at 50 °C overnight. This gave 3.165 g (yield = 65%) of material with a purity of 99.9% by HPLC.

[0292] Synthesis of deuterated mixtures of DMT compounds A modified synthesis in stage 2 using a solid LiAlH4 / LiAlD4 mixture was employed using 1.8 equivalents of LiAlH4 / LiAlD4 versus 0.9 equivalents using the method described above for undeuterated DMT. Six deuteration reactions were carried out.

[0293] Representative synthesis of a deuterated mixture of DMT compounds (using 1:1 LiAlH4:LiAlD4) A 250 mL three-neck flask under N2 was charged with LiAlH4 (1.013 g, 26.7 mmol), LiAlD4 (1.120 g, 26.7 mmol), and THF (100 mL). The resulting suspension was stirred for 30 min before Stage 1 (6 g, 29.666 mmol) was added dropwise over 15 min at 20–40 °C. The reaction mixture was then heated at reflux (66 °C) for 2 h, at which point HPLC indicated no Stage 1 remained. The mixture was cooled to 0 °C and quenched with 25% Rochelle's salt (aq) (120 mL) over 30 min below 30 °C. The resulting milky suspension was stirred for 1 h and then allowed to separate. The lower aqueous layer was removed, and the upper organic layer was washed with saturated brine (30 mL). The organics were then dried over MgSO4, filtered, and concentrated in vacuo. This yielded 4.3 g of crude material. The crude material was then taken up in ethanol (52 mL) and charged with fumaric acid (2.66 g, 22.917 mmol) before heating to 75°C. The resulting solution was allowed to cool to ambient temperature overnight before further cooling to 0-5°C for 1 hour. The solid was isolated by filtration and washed with cold ethanol (6.5 mL x 2). The filter cake was dried at 50°C overnight to give 5.7 g (yield = 63%) of product with a purity of 99.9% by HPLC and >95% by NMR.

[0294] Evaluation of the degree of deuteration This was performed by LCMS-SIM (SIM = single ion monitoring), and analysis yielded isolated ion counts for each mass of the tritiated N,N-dimethyltryptamine compounds (N,N-dimethyltryptamine (DO), α-deutero-N,N-dimethyltryptamine (D1), and α,α-dideutero-N,N-dimethyltryptamine (D2)) at the retention time of N,N-dimethyltryptamine. The percentage of each component was then calculated from these ion counts. For example, %D0 = [D0 / (D0+D1+D2)] x 100

[0295] HPLC parameters System: Agilent 1100 / 1200 series liquid chromatograph or equivalent Column: Triart Phenyl; 150 x 4.6 mm, 3.0 μm particle size (Ex: YMC, Part number: TPH12S03-1546PTH) Mobile phase A: Water: Trifluoroacetic acid (100:0.05%) Mobile phase B: acetonitrile:trifluoroacetic acid (100:0.05%) Gradient: Time %A %B 0 95 5 13 62 38 26 5 95 30.5 5 95 31 95 5 Flow rate: 1.0mL / min Stop time: 31 minutes After execution: 4 minutes Injection volume: 5μl Wash vial: N / A Column temperature: 30℃ Wavelength: 200nm,(4nm) Reference: N / A

[0296] Mass spectrometry parameters System: Agilent 6100 Series Quadrupole LC-MS or equivalent Drying gas flow: 12.0 L / min Drying gas temperature: 350°C Sprayer pressure: 35 psig Fragmentor: 110 Gain: 1.00

[0297] Cpd RT RRT Concentration Diluent Detection Mass DO 10.64 1.00 0.30mg / ml CH3CN:H20(50:50) (+)SIM 189.10m / z D1 10.64 1.00 0.30mg / ml CH3CN:H20(50:50) (+)SIM 190.10m / z D2 10.64 1.00 0.30mg / ml CH3CN:H20(50:50) (+)SIM 191.10m / z The MS-SIM range is the target mass ±0.1 m / z.

[0298] Data for six deuterated reactants are shown in Table 2 below: [Table 2]

[0299] In vitro intrinsic clearance of a mixture of DMT (SPL026) and six deuterated compounds In vitro measurements of intrinsic clearance are a valuable model for predicting in vivo hepatic clearance. The liver is the major organ for drug metabolism in the body and contains both phase I and phase II drug-metabolizing enzymes present in intact cells.

[0300] the purpose Human hepatocytes are used to assess the in vitro intrinsic clearance of a mixture of deuterated DMT analogs relative to DMT.

[0301] Experiment Description The in vitro intrinsic clearance of DMT and six deuterated analogs was investigated using pooled human (mixed-gender) hepatocytes from 10 donors (0.545 million cells / mL).

[0302] All test compounds, as well as sumatriptan, serotonin, and benzylamine controls, were used at a concentration of 5 μM. This concentration was chosen to maximize signal-to-noise while maintaining the Michaelis constant (Km) for monoamine oxidase (MAO). Diltiazem and diclofenac controls were used at their laboratory-validated concentration of 1 μM.

[0303] Test compounds were mixed with hepatocyte suspensions in 96-well plates and incubated at 37°C for 60 minutes. The suspensions were continuously stirred. At seven time points, small aliquots were removed and the test compound / blend concentrations were measured by LC-MS / MS. The measured time points were 2, 4, 8, 15, 30, 45, and 60 minutes.

[0304] The following LC-MS / MS conditions were used for the analysis: Instrument: Thermo TSQ Quantiva with Thermo Vanquish UPLC system Column: Luna Omega 2.1x50mm 2.6μm Solvent A: HO + 0.1% formic acid Solvent B: Acetonitrile + 0.1% formic acid Flow rate: 0.8ml / min Injection volume: 1μl Column temperature: 65℃ gradient: [Table 2-1] MS parameters: Positive ion spray voltage: 4000V Vaporizer temperature: 450℃ Ion transfer tube temperature: 365℃ Sheath Gas: 54 Auxiliary gas: 17 Sweep gas: 1 Dwell time 8 ms MRM transition: DO = Mass to Fill Ratio 189.14>58.16 D1=Mass to Fill Ratio 190.14>59.17 · D2=mass to filling ratio 191.14>60.17

[0305] MRM transitions were determined from preliminary analyses of DMT samples containing either no deuterium (for D0 transitions) or high levels of D1 or D2 deuteration (for D1 and D2 transitions, respectively).

[0306] The resulting concentration-time profile was then analyzed to determine the intrinsic clearance (CLint) and half-life (t 1 / 2 ) was used to calculate the elimination rate constant (IL) for each analyte. To do this, the MS peak area or MS peak area / IS response for each analyte is plotted on a natural log scale on the y-axis against sampling time (minutes) on the x-axis. The slope of this line is the elimination rate constant. This is converted to half-life by -ln(2) / slope. The intrinsic clearance is calculated from the slope / elimination rate constant by the formula: CLint = (-1000 * gradient) / cell density (1E6 cells / ml), giving units of microliters / minute / million cells.

[0307] result Intrinsic clearance and half-life values ​​were calculated for DMT and the six deuterated mixtures listed above. These data were weighted according to the proportions of D0, D1, and D2 to obtain overall intrinsic clearance and half-life values ​​for each compound mixture (Table 3).

[0308] [Table 3]

[0309] The data were fitted with a linear model using regression analysis, which revealed that deuterium enrichment at the α-carbon of DMT linearly decreases intrinsic clearance with increasing molecular weight (MW), thereby enabling the production of DMT drug substances with accurately predictable half-lives within the identified range.

[0310] The greatest change was observed in Mix 1, which contained 96.6% D2-DMT, nearly halving the intrinsic clearance rate (Figure 4) and nearly doubling the half-life compared to non-deuterated DMT (Figure 3). Intermediate deuterated mixes (Mixes 2–5) reduced intrinsic clearance in a manner correlated with molecular weight (Figure 4).

[0311] conclusion These data demonstrate that increasing deuterium enrichment at the α-carbon of DMT increases metabolic stability, resulting in reduced clearance and a longer half-life. In particular, when the input reducing agent for the production of deuterium-enriched DMT-containing drug substances by the methods of the present invention contains LiAlH4 and LiAlD4 in a ratio of 1:2.5 to 2.5:1, a linear relationship exists between MW and half-life. The relative half-lives of similar mixtures of protio-, mono-, and di-deutero compounds of Formula I are expected to mirror the trends observed here for mixtures of protio-, mono-, and di-deutero DMT. Increasing deuterium enrichment at the α-carbon of compounds of Formula I is expected to increase metabolic stability, resulting in reduced clearance and a longer half-life.

[0312] The best aspects of DMT Stage 1 [Table 4-1]

[0313] [Table 4-2]

[0314] [Table 4-3]

[0315] [Table 4-4]

[0316] [Table 4-5]

[0317] [Table 4-6]

[0318]

Table 4-7

[0319]

Table 4-8

[0320]

Table 4-9

[0321]

Table 4-10

[0322]

Table 4-11

[0323]

Table 4-12

[0324]

Table 4-13

[0325]

Table 4-14

Claims

1. 1. A pharmaceutical composition for use in hallucinogenic-assisted psychotherapy, the composition comprising, as an active ingredient, a compound of formula I: 【Chemical 1】 (In the above formula, ｘ H is protium or deuterium; n is selected from 1, 2, 3 or 4; R １ is -R ３ , -OR ３ , -O(CO)R ３ , —F, —Cl, —Br, or —I; and R ２ and R ３ are independently １ -C ４ alkyl, provided that n is 1 and R 1 When is 5-methoxy, xH is protium. A pharmaceutical composition comprising the compound of formula (I).

2. n is 1, R 1 is at the 5-position, R 1 is independently selected from —R 3 , —OR 3 , and —O(CO)R 3 ; The composition of claim 1.

3. R ２ The composition of claim 1 or 2, wherein is methyl.

4. R １ But OR ３ and -O(CO)R ３ and / or R ３ is methyl, and / or R １ The composition of any one of claims 1 to 3, wherein is methoxy and / or n is 1.

5. A pharmaceutical composition for use in a method for treating a psychiatric or neurological disorder in a patient, the composition comprising, as an active ingredient, a compound of formula I: 【Chemistry 2】 (where xH is protium or deuterium; n is selected from 1, 2, 3 or 4; R 1 is independently selected from —R 3 , —OR 3 , —O(CO)R 3 , —F, —Cl, —Br, or —I; and R 2 and R 3 are independently selected from C 1 -C 4 alkyl, provided that n is 1 and R 1 When is 5-methoxy, xH is protium. A pharmaceutical composition comprising the compound of formula (I).

6. n is 1, R 1 is at the 5-position, R 1 is independently selected from —R 3 , —OR 3 , and —O(CO)R 3 ; The composition of claim 5.

7. The composition of claim 5 or 6, wherein R 2 is methyl.

8. The composition according to claim 5, wherein R 1 is independently selected from OR 3 and —O(CO)R 3 , and / or R 3 is methyl, and / or R 1 is methoxy, and / or n is 1.

9. The psychiatric or neurological disorder is (a) selected from (i) obsessive-compulsive disorder, (ii) depressive disorder, (iii) schizophrenia, (iv) schizophrenia-type disorder, (v) anxiety disorder, (vi) substance abuse, and (vii) anorexia disorder; or (b) major depressive disorder; or (c) Treatment-resistant depression The composition according to any one of claims 5 to 8.

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