CN107759620B - Octahydropyrrolo [3,4-c ] pyrrole derivatives, methods of use, and uses thereof - Google Patents

Abstract

The invention relates to octahydropyrrolo [3,4-c ] pyrrole derivatives, methods of use and uses thereof, compounds of the invention and pharmaceutical compositions comprising the compounds for antagonizing orexin receptors. The invention also relates to processes for preparing such compounds and pharmaceutical compositions, and to their use in the treatment or prevention of diseases in which orexin receptors are involved.

Description

Octahydropyrrolo [3,4-c ] pyrrole derivatives, methods of use, and uses thereof

Technical Field

The invention belongs to the technical field of medicines, and particularly relates to substituted (octahydropyrrolo [3,4-c ] pyrrole-2 (1H) -yl) phenyl ketone compounds, a pharmaceutical composition containing the compounds, and a use method and application of the compounds. More particularly, the compounds and pharmaceutical compositions described herein are useful as orexin receptor antagonists for the treatment, prevention or alleviation of orexin receptor related disorders.

Background

Orexin (orexin), also known as hypothalamin, orexin, which includes orexin a and orexin B (or hypothalamin-1 and hypothalamin-2), is a neuropeptide secreted by the hypothalamus with its main physiological roles: 1. appetite regulation, orexin can significantly promote food intake and exhibit a dose-dependent response, and activates the neurons that regulate food intake; 2. participating in the regulation of energy metabolism, the orexin can obviously increase the metabolic rate; 3. participating in sleep-wake regulation, orexin can inhibit rapid eye movement sleep, prolong wake time, and block orexin effect to promote sleep; 4. participating in endocrine regulation, and the influence of the orexin on the endocrine of pituitary hormone is obvious; 5. associated with sense of reward, learning, and memory; 6. promoting gastric acid secretion; 7. promoting the increase of drinking water; 8. raising blood pressure; 9. plays an important role in reward systems and drug addiction mechanisms, among others (Piper et al, The novel blue neuroepidetide, orexin-A, models The sleep-wave cycle of rates. Eur. J. Neuroscience,2000,12(2), 726-730; and Sakurai, T. et al, The neural circuit of orexin. Nature Review Neuroscience,2007,8: 171181). While in biological importance, orexin a is more important than orexin B, e.g., orexin a enhances feeding behavior after an animal is nutritionally restricted; the agitation level of rats can be increased by injecting orexin A into ventricles of the brain; the regulation of the activity of the orexin A on the locus coeruleus provides important support for cognitive processes such as attention, memory and the like; orexin a may also ameliorate the memory impairment caused by amyloid beta; orexin A has effect of improving dysmnesia caused by sleep deprivation; orexin a is associated with sleep disturbance in some patients with brain-related disorders; and orexin a receptors that modulate the relapse of cocaine.

Orexin produces physiological effects by acting on orexin receptors (OXR). The orexin receptor is a G-protein coupled receptor of two types, respectively called OX₁Receptors and OX₂Receptor of which OX₁The receptor is selective for orexin A, and OX₂The receptor is a nonselective receptor for orexin A and orexin B (Sakurai T. et al., Orexins and orexin receptors: a family of hypothalamic neuroreceptors and G protein-coupled receptors which are not involved in regulation of behavior. cell,1998,92(4):573 585). OX₁Receptors and OX₂Receptors are present almost exclusively in brain tissue and are selectively expressed in the brain, where OX₁Receptors are expressed in high density in locus coeruleus (blue specks), which is the initiation of noradrenergic neurons, and OX₂Receptors are expressed in high density in the nuclei of the papillary nodules, which are the initiation nuclei of histaminergic neurons. OX₁Receptors and OX₂Expression of both receptors is seen in the mid-slit nucleus, which is the initiation of serotonergic neurons, and in the ventral tegmental area, which is the initiation of dopaminergic neurons.

Thus, it can be seen that orexin receptors are pathologically important in relation to a variety of diseases such as sleep disorders, depression, anxiety disorders, panic disorders, obsessive-compulsive disorders, affective neuropathies, depressive neuropathies, anxiety neuropathies, mood disorders, panic attack disorders, behavioral disorders, mood disorders, post-traumatic stress disorders, sexual dysfunction, psychosis, schizophrenia, manic depression, confusion, dementia, drug dependence, addiction, cognitive disorders, alzheimer's disease, parkinson's disease, movement disorders, eating disorders, headache, migraine, pain, digestive system diseases, epilepsy, inflammation, cardiovascular diseases, diabetes, metabolic diseases, immune-related diseases, endocrine-related diseases and hypertension. However, the only drugs currently on the market related to the orexin receptor are Suvorexant (Suvorexant), an anti-insomnia drug developed by american merck corporation, which is an orexin receptor antagonist, and which have once been subject to approval by the us FDA due to safety issues.

In view of this, novel orexin receptor antagonists, particularly selective OX, were developed₁Receptor antagonists are of great interest in the treatment of diseases associated with the orexin receptor. The present invention provides a class of compounds having orexin receptor antagonistic activity on OX, as compared to existing analogues₁The receptor shows selectivity, has better pharmacodynamic activity, less toxic and side effects and higher safety, and also has excellent physicochemical property, pharmacokinetic property and toxicological property, so the receptor has better clinical application prospect.

Disclosure of Invention

The following is a summary of some aspects of the invention only and is not intended to be limiting. These aspects and others are described more fully below. All references in this specification are incorporated herein by reference in their entirety. When the disclosure of the present specification differs from the cited documents, the disclosure of the present specification controls.

The invention provides a compound with orexin receptor antagonistic activity, in particular to an octahydropyrrolo [3,4-c ] pyrrole derivative and a pharmaceutical composition thereof, wherein the compound and the pharmaceutical composition can be used for preparing medicines for preventing or treating diseases related to orexin receptors.

The compounds of the invention exhibit good antagonistic activity against orexin receptors, in particular OX₁The receptor exhibits selectivity and thus has better pharmacodynamic, pharmacokinetic and/or toxicological properties, such as a good brain/plasma ratio (br)ain plasma ratio), good bioavailability, good metabolic stability, low toxic and side effects, high safety and the like. At the same time, the excellent properties of certain parameters of the compounds of the invention, such as half-life, clearance, selectivity, bioavailability, chemical stability, metabolic stability, membrane permeability, solubility, etc., can contribute to a reduction in side effects, an expansion of the therapeutic index or an improvement in tolerance.

Specifically, the method comprises the following steps:

in one aspect, the invention relates to a compound that is a compound of formula (I) or a stereoisomer, tautomer, nitrogen oxide, solvate, metabolite, pharmaceutically acceptable salt, or prodrug of a compound of formula (I),

wherein:

hy is triazolyl optionally substituted with one or more groups independently selected from D, F, Cl, Br, I, oxo (═ O), C_1-6Alkyl radical, C_1-6Haloalkyl, C_1-6Alkoxy radical, C_1-6Haloalkoxy or benzyl; and

R¹、R²、R³、R⁴、R⁵、R⁶、R⁷、R⁸and R⁹Each having the meaning as described in the present invention.

In one embodiment, the present invention relates to a compound that is a compound of formula (II) or a stereoisomer, a tautomer, a nitrogen oxide, a solvate, a metabolite, a pharmaceutically acceptable salt, or a prodrug of a compound of formula (II),

wherein R is¹、R²、R³、R⁴、R⁵、R⁶、R⁷、R⁸And R⁹Each having the meaning as described in the present invention.

In one embodiment, R in formula (I) or formula (II)¹、R²、R³、R⁴And R⁵Each independently is H, D, -CD₃、F、Cl、Br、I、-CN、-NH₂、-OH、-NO₂、-COOH、-C(＝O)NH₂、C_1-6Alkyl radical, C_2-6Alkenyl radical, C_2-6Alkynyl, C_1-6Haloalkyl, C_1-6Alkoxy radical, C_1-6Haloalkoxy, C_1-6Alkylamino radical, C_1-6Hydroxy-substituted alkyl, -C (═ O) - (C)_1-6Alkyl), -C (═ O) - (C)_1-6Alkoxy), -C (═ O) - (C)_1-6Alkylamino), -O- (CH)₂)_n-C(＝O)O-(C_1-6Alkyl), -O- (CH)₂)_n-COOH、-O-(CH₂)_n-C(＝O)NH₂、C_3-6Cycloalkyl radical, C_2-9Heterocyclic group, C_6-10Aryl or C_1-9A heteroaryl group; and each n is independently 1,2,3 or 4.

In one embodiment, R in formula (I) or formula (II)⁶、R⁷、R⁸And R⁹Each independently is H, D, F, Cl, Br, I, -CN, -NH₂、-OH、-NO₂、-COOH、-C(＝O)NH₂、C_1-6Alkyl radical, C_2-6Alkenyl radical, C_2-6Alkynyl, C_1-6Haloalkyl, C_1-6Alkoxy radical, C_1-6Haloalkoxy, C_1-6Alkylamino radical, C_1-6Hydroxy-substituted alkyl, -C (═ O) - (C)_1-6Alkyl), -C (═ O) - (C)_1-6Alkoxy), -C (═ O) - (C)_1-6Alkylamino), C_3-6Cycloalkyl radical, C_2-9Heterocyclic group, C_6-10Aryl or C_1-9A heteroaryl group.

In one embodiment, R in formula (I) or formula (II)¹、R²、R³、R⁴And R⁵Each independently is H, D, -CD₃、F、Cl、Br、I、-CN、-NH₂、-OH、-NO₂、-COOH、-C(＝O)NH₂、C_1-4Alkyl radical, C_2-4Alkenyl radical, C_2-4Alkynyl, C_1-4Haloalkyl, C_1-4Alkoxy radical, C_1-4Haloalkoxy, C_1-4Alkylamino radical, C_1-4Hydroxy-substituted alkyl, -C (═ O) - (C)_1-4Alkyl), -C (═ O) - (C)_1-4Alkoxy), -C (═ O) - (C)_1-4Alkylamino), -O- (CH)₂)_n-C(＝O)O-(C_1-4Alkyl), -O- (CH)₂)_n-COOH or-O- (CH)₂)_n-C(＝O)NH₂。

In one embodiment, R in formula (I) or formula (II)⁶、R⁷、R⁸And R⁹Each independently is H, D, F, Cl, Br, I, -CN, -NH₂、-OH、-NO₂、-COOH、-C(＝O)NH₂、C_1-4Alkyl radical, C_2-4Alkenyl radical, C_2-4Alkynyl, C_1-4Haloalkyl, C_1-4Alkoxy radical, C_1-4Haloalkoxy, C_1-4Alkylamino radical, C_1-4Hydroxy-substituted alkyl, -C (═ O) - (C)_1-4Alkyl), -C (═ O) - (C)_1-4Alkoxy) or-C (═ O) - (C)_1-4Alkylamino).

In one embodiment, R in formula (I) or formula (II)¹、R²、R³、R⁴And R⁵Each independently is H, D, -CD₃、F、Cl、Br、I、-CN、-NH₂、-OH、-NO₂、-COOH、-C(＝O)NH₂Methyl, ethyl, n-propyl, isopropyl, -CF₃、-CH₂CF₃、-CF₂CF₃Methoxy, ethoxy, n-propyloxy, isopropyloxy, -NHCH₃、-N(CH₃)₂、-CH₂OH、-C(＝O)NHCH₃、-C(＝O)N(CH₃)₂、-O-CH₂-C(＝O)O-CH₃、-O-(CH₂)₂-C(＝O)O-CH₃、-O-CH₂-C(＝O)O-CH₂CH₃、-O-(CH₂)₂-C(＝O)O-CH₂CH₃、-O-CH₂-C(＝O)O-CH₂CH₂CH₃、-O-(CH₂)₂-C(＝O)O-CH₂CH₂CH₃、-O-CH₂-C(＝O)O-CH(CH₃)₂、-O-(CH₂)₂-C(＝O)O-CH(CH₃)₂、-O-CH₂-COOH、-O-(CH₂)₂-COOH、-O-CH₂-C(＝O)NH₂or-O- (CH)₂)₂-C(＝O)NH₂。

In one embodiment, R in formula (I) or formula (II)⁶、R⁷、R⁸And R⁹Each independently is H, D, F, Cl, Br, I, -CN, -NH₂、-OH、-NO₂、-COOH、-C(＝O)NH₂Methyl, ethyl, n-propyl, isopropyl, -CF₃、-CH₂CF₃、-CF₂CF₃Methoxy, ethoxy, n-propyloxy, isopropyloxy, -NHCH₃、-N(CH₃)₂or-CH₂OH。

In one embodiment, the compound of the present invention, which is a compound having one of the following structures or a stereoisomer, tautomer, nitrogen oxide, solvate, metabolite, pharmaceutically acceptable salt or prodrug of a compound having one of the following structures,

in another aspect, the invention relates to a pharmaceutical composition comprising a compound of the invention.

In one embodiment, the pharmaceutical composition of the present invention optionally comprises a pharmaceutically acceptable carrier, excipient, adjuvant, or any combination thereof.

In another aspect, the invention relates to the use of a compound or pharmaceutical composition described herein for the manufacture of a medicament for the prevention, treatment or alleviation of diseases or disorders associated with orexin receptors.

In one embodiment, the orexin receptor-related disease is sleep disorder, depression, anxiety disorder, panic disorder, obsessive-compulsive disorder, affective neuropathy, depressive neuropathy, anxiety neuropathy, mood disorder, panic attack disorder, behavioral disorders, mood disorder, post-traumatic stress disorder, sexual dysfunction, psychosis, schizophrenia, manic depression, delirium, dementia, drug dependence, addiction, cognitive disorder, alzheimer's disease, parkinson's disease, movement disorder, eating disorder, headache, migraine, pain, digestive system disease, epilepsy, inflammation, cardiovascular disease, diabetes, metabolic disease, immune-related disease, endocrine-related disease or hypertension.

In another aspect, the invention relates to the use of a compound or pharmaceutical composition according to the invention in the manufacture of a medicament for antagonizing orexin receptors.

In another aspect, the invention relates to a process for the preparation, isolation and purification of a compound encompassed by formula (I) or formula (II).

Biological test results show that the compound provided by the invention can be used as a better orexin receptor antagonist, particularly as selective OX₁A receptor antagonist.

Any embodiment of any aspect of the invention may be combined with other embodiments, as long as they do not contradict. Furthermore, in any embodiment of any aspect of the invention, any feature may be applicable to that feature in other embodiments, so long as they do not contradict.

The foregoing merely summarizes certain aspects of the invention and is not intended to be limiting. These and other aspects will be more fully described below.

Disclosure of Invention

Definitions and general terms

Reference will now be made in detail to certain embodiments of the invention, examples of which are illustrated by the accompanying structural and chemical formulas. The invention is intended to cover alternatives, modifications and equivalents, which may be included within the scope of the invention as defined by the appended claims. One skilled in the art will recognize that many methods and materials similar or equivalent to those described herein can be used in the practice of the present invention. The present invention is in no way limited to the methods and materials described herein. In the event that one or more of the incorporated documents, patents, and similar materials differ or contradict this application (including but not limited to defined terminology, application of terminology, described techniques, and the like), this application controls.

It will be further appreciated that certain features of the invention, which are, for clarity, described in the context of separate embodiments, may also be provided in combination in a single embodiment. Conversely, various features of the invention which are, for brevity, described in the context of a single embodiment, may also be provided separately or in any suitable subcombination.

Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. All patents and publications referred to herein are incorporated by reference in their entirety.

The articles "a," "an," and "the" as used herein are intended to include "at least one" or "one or more" unless otherwise indicated or clearly contradicted by context. Thus, as used herein, the articles refer to one or to more than one (i.e., to at least one) of the objects. For example, "an embodiment" refers to one or more embodiments.

The term "optional" or "optionally" means that the subsequently described event or circumstance may, but need not, occur, and that the description includes instances where said event or circumstance occurs and instances where it does not.

The term "optionally substituted with … …" is used interchangeably with the term "unsubstituted or substituted with … …", i.e., the structure or group is unsubstituted or substituted with one or more substituents described herein, wherein the substitution is meant to occur on any given structure or groupReasonable position allowed by valence. Substituents described herein include, but are not limited to, D, F, Cl, Br, I, -N₃、-CN、-NO₂、-OH、-SH、-NH₂Alkyl, alkenyl, alkynyl, haloalkyl, alkoxy, alkylthio, alkylamino, cycloalkyl, heterocyclyl, aryl, heteroaryl, and the like.

In general, the term "substituted" means that one or more hydrogen atoms in a given structure or group are replaced with a particular substituent. Unless otherwise indicated, a substituent may be substituted at any reasonable position in the group that it may be substituted for. When more than one position in a given formula can be substituted with one or more particular substituents selected from the group, the substituents may be identically or differently substituted at each of the possible positions in the formula.

The term "comprising" is open-ended, i.e. includes the elements indicated in the present invention, but does not exclude other elements.

In the various parts of this specification, substituents of the disclosed compounds are disclosed in terms of group type or range. It is specifically intended that the invention includes each and every independent subcombination of the various members of these groups and ranges. For example, the term "C_1-6Alkyl "means in particular independently disclosed methyl, ethyl, C₃Alkyl radical, C₄Alkyl radical, C₅Alkyl and C₆An alkyl group.

The term "D" denotes a single deuterium atom.

The term "heteroatom" denotes one or more of oxygen (O), sulfur (S), nitrogen (N), phosphorus (P) or silicon (Si), including nitrogen (N), sulfur (S) and phosphorus (P) in any oxidation state; primary, secondary, tertiary amines and quaternary ammonium salt forms; or a form in which a hydrogen on a nitrogen atom in the heterocycle is substituted, for example, N (like N in 3, 4-dihydro-2H-pyrrolyl), NH (like NH in pyrrolidinyl) or NR (like NR in N-substituted pyrrolidinyl).

The terms "halogen" and "halo" are used interchangeably herein to refer to fluorine (F), chlorine (Cl), bromine (Br), or iodine (I).

The term "alkyl" or "alkyl group" as used herein, tableAre saturated, straight or branched chain monovalent hydrocarbon radicals containing from 1 to 20 carbon atoms, wherein the alkyl radicals may be optionally substituted with one or more substituents described herein. In one embodiment, the alkyl group contains 1 to 6 carbon atoms; in another embodiment, the alkyl group contains 1 to 4 carbon atoms; in yet another embodiment, the alkyl group contains 1 to 3 carbon atoms. Examples of alkyl groups include, but are not limited to, methyl (Me, -CH)₃) Ethyl group (Et, -CH)₂CH₃) N-propyl (n-Pr, -CH)₂CH₂CH₃) Isopropyl group (i-Pr, -CH (CH)₃)₂) N-butyl (n-Bu, -CH)₂CH₂CH₂CH₃) Isobutyl (i-Bu, -CH)₂CH(CH₃)₂) Sec-butyl (s-Bu, -CH (CH)₃)CH₂CH₃) Tert-butyl (t-Bu, -C (CH)₃)₃) And so on.

The term "alkenyl" denotes a straight or branched chain monovalent hydrocarbon radical containing 2 to 12 carbon atoms, wherein there is at least one site of unsaturation, i.e. one carbon-carbon sp²A double bond, wherein the alkenyl group is optionally substituted with one or more substituents described herein, including the positioning of "cis" and "trans", or the positioning of "E" and "Z".

The term "alkynyl" denotes a straight or branched chain monovalent hydrocarbon radical containing 2 to 12 carbon atoms, wherein there is at least one site of unsaturation, i.e. one carbon-carbon sp triple bond, wherein said alkynyl radical is optionally substituted with one or more substituents as described herein.

The term "alkoxy" means an alkyl group attached to the rest of the molecule through an oxygen atom, wherein the alkyl group has the meaning as described herein. Unless otherwise specified, the alkoxy group contains 1 to 12 carbon atoms. In one embodiment, the alkoxy group contains 1 to 6 carbon atoms; in another embodiment, the alkoxy group contains 1 to 4 carbon atoms; in yet another embodiment, the alkoxy group contains 1 to 3 carbon atoms. The alkoxy group may be optionally substituted with one or more substituents described herein.

Examples of alkoxy groups include, but are not limited to, methoxy (MeO, -OCH)₃) Ethoxy (EtO, -OCH)₂CH₃) 1-propoxy (n-PrO, n-propoxy, -OCH)₂CH₂CH₃) 2-propoxy (i-PrO, i-propoxy, -OCH (CH)₃)₂) 1-butoxy (n-BuO, n-butoxy, -OCH)₂CH₂CH₂CH₃) 2-methyl-l-propoxy (i-BuO, i-butoxy, -OCH)₂CH(CH₃)₂) 2-butoxy (s-BuO, s-butoxy, -OCH (CH)₃)CH₂CH₃) 2-methyl-2-propoxy (t-BuO, t-butoxy, -OC (CH)₃)₃) And so on.

The term "haloalkyl" denotes an alkyl group substituted with one or more halogen atoms, wherein the alkyl group has the meaning as described herein, examples of which include, but are not limited to, -CF₃、-CF₂CF₃、-CH₂CF₂CHF₂And the like. In one embodiment, "haloalkyl" is a lower C_1-4Haloalkyl, wherein said "C_1-4Haloalkyl "comprises fluorine substituted C_1-4Alkyl, chloro-substituted C_1-4Alkyl, bromo substituted C_1-4Alkyl, iodo substituted C_1-4Alkyl, and the like. In particular, fluorine substituted C_1-4The alkyl group containing-CH₂F、-CHF₂、-CF₃、-CH₂Cl、-CHCl₂、-CCl₃、-CH₂Br、-CHBr₂、-CBr₃、-CH₂CH₂F、-CH₂CHF₂、-CH₂CF₃、-CF₂CH₂F、-CF₂CHF₂、-CF₂CF₃、-CHFCF₃、-CHFCHF₂、-CHFCH₂F、-CH₂CH₂CF₃、-CH₂CF₂CHF₂And so on. The haloalkyl is optionally substituted with one or more substituents described herein.

The term "haloalkoxy" denotes alkoxyThe groups being substituted by one or more halogen atoms, where the alkoxy group has the meaning as described in the present invention, such examples include, but are not limited to, -OCF₃、-OCF₂CF₃、-OCH₂CF₂CHF₂And the like. The haloalkoxy group is optionally substituted with one or more substituents described herein.

The term "alkylamino" or "alkylamino" includes "N-alkylamino" and "N, N-dialkylamino" wherein the amino groups are each independently substituted with one or two alkyl groups, wherein the alkyl groups have the meaning as described herein.

The term "hydroxy-substituted alkyl" means that the alkyl group is substituted with one or more hydroxy groups, wherein the alkyl group has the meaning described herein. Examples include, but are not limited to, hydroxymethyl, hydroxyethyl, 1, 2-dihydroxyethyl, and the like.

The terms "carbocyclyl" or "carbocycle" are used interchangeably herein and refer to a mono-or polyvalent monocyclic, bicyclic, or tricyclic ring system containing from 3 to 12 ring carbon atoms, wherein the ring may be fully saturated or contain one or more unsaturations, but not one aromatic ring.

The terms "heterocyclyl" and "heterocycle" are used interchangeably herein and refer to a mono-, bi-or tricyclic monovalent or multivalent ring system containing 3 to 12 ring atoms, wherein one or more atoms in the ring are independently replaced by a heteroatom having the meaning described herein, which ring may be fully saturated or contain one or more unsaturations, but not one aromatic ring.

The term "cycloalkyl" denotes a monovalent or polyvalent saturated monocyclic, bicyclic or tricyclic ring system containing from 3 to 12 ring carbon atoms.

The term "aryl" denotes a mono-, bi-or tricyclic mono-, carbocyclic ring system containing 6 to 14 ring atoms, or 6 to 10 ring atoms, or 6 ring atoms, wherein at least one ring is aromatic. The aryl group is typically, but not necessarily, attached to the parent molecule through an aromatic ring of the aryl group. The term "aryl" may be used interchangeably with the terms "aromatic ring" or "aromatic ring". Examples of aryl groups can include phenyl, naphthyl, anthracene, and the like. The aryl group is optionally substituted with one or more substituents described herein.

The term "heteroaryl" denotes a mono-, bi-or tricyclic ring system containing 5 to 14 ring atoms, or 5 to 10 ring atoms, or 5 to 6 ring atoms (i.e., 5 to 6 membered), monovalent or multivalent, wherein at least one ring is aromatic and at least one ring contains one or more heteroatoms. The heteroaryl group is typically, but not necessarily, attached to the parent molecule through an aromatic ring of the heteroaryl group. The term "heteroaryl" may be used interchangeably with the terms "heteroaromatic ring" or "heteroaromatic compound". The heteroaryl group is optionally substituted with one or more substituents described herein.

Examples of heteroaryl groups include, but are not limited to, 2-furyl, 3-furyl, N-imidazolyl, 2-imidazolyl, 4-imidazolyl, 5-imidazolyl, 3-isoxazolyl, 4-isoxazolyl, 5-isoxazolyl, 2-oxazolyl, 4-oxazolyl, 5-oxazolyl, N-pyrrolyl, 2-pyrrolyl, 3-pyrrolyl, 2-pyridyl, 3-pyridyl, 4-pyridyl, 2-pyrimidinyl, 4-pyrimidinyl, 5-pyrimidinyl, pyridazinyl (e.g., 3-pyridazinyl), 2-thiazolyl, 4-thiazolyl, 5-thiazolyl, tetrazolyl (e.g., 5-tetrazolyl), triazolyl (e.g., 2-triazolyl and 5-triazolyl), and the like, 2-thienyl, 3-thienyl, pyrazolyl (e.g., 2-pyrazolyl), isothiazolyl, 1,2, 3-oxadiazolyl, 1,2, 5-oxadiazolyl, 1,2, 4-oxadiazolyl, 1,2, 3-triazolyl, 1,2, 3-thiadiazolyl, 1,3, 4-thiadiazolyl, 1,2, 5-thiadiazolyl, pyrazinyl, 1,3, 5-triazinyl; the following bicyclic rings are also included, but are in no way limited to these: benzimidazolyl, benzofuranyl, benzothienyl, indolyl (e.g., 2-indolyl), purinyl, quinolyl (e.g., 2-quinolyl, 3-quinolyl, 4-quinolyl), isoquinolyl (e.g., 1-isoquinolyl, 3-isoquinolyl, or 4-isoquinolyl), imidazo [1,2-a ] pyridyl, pyrazolo [1,5-a ] pyrimidinyl, imidazo [1,2-b ] pyridazinyl, [1,2,4] triazolo [4,3-b ] pyridazinyl, [1,2,4] triazolo [1,5-a ] pyrimidinyl, [1,2,4] triazolo [1,5-a ] pyridyl, and the like.

As described herein, the attachment point may be attached to the rest of the molecule at any point on the ring where it can be attached. For example, Hy in the present invention may be a triazolyl group, any position on the triazolyl group that can be attached may be used as a point of attachment to the rest of the molecule, including in particular the sub-formulae i-1 to i-14:

the term "stereoisomers" refers to compounds having the same chemical structure, but differing in the arrangement of atoms or groups in space. Stereoisomers include enantiomers, diastereomers, conformers (rotamers), geometric isomers (cis/trans), atropisomers, and the like.

The stereochemical definitions and rules used in the present invention generally follow the general definitions of S.P. Parker, Ed., McGraw-Hill Dictionary of Chemical Terms (1984) McGraw-Hill Book Company, New York; and Eliel, E.and Wilen, S, "Stereochemistry of Organic Compounds", John Wiley & Sons, Inc, New York, 1994. Many organic compounds exist in an optically active form, i.e., they have the ability to rotate the plane of plane polarized light. In describing optically active compounds, the prefixes D and L or R and S are used to denote the absolute configuration of a molecule with respect to one or more of its chiral centers. The prefixes d and l or (+) and (-) are the symbols used to specify the rotation of plane polarized light by the compound, where (-) or l indicates that the compound is left-handed. Compounds prefixed with (+) or d are dextrorotatory. A particular stereoisomer is an enantiomer and a mixture of such isomers is referred to as an enantiomeric mixture. A50: 50 mixture of enantiomers is referred to as a racemic mixture or racemate, which may occur when there is no stereoselectivity or stereospecificity in the chemical reaction or process.

Any resulting mixture of stereoisomers may be separated into pure or substantially pure geometric isomers, enantiomers, diastereomers, depending on differences in the physicochemical properties of the components, for example, by chromatography and/or fractional crystallization.

The racemates of any of the resulting end products or intermediates can be resolved into the optical enantiomers by known methods using methods familiar to those skilled in the art, e.g., by separation of the diastereomeric salts obtained. The racemic product can also be separated by chiral chromatography, e.g., High Performance Liquid Chromatography (HPLC) using a chiral adsorbent. In particular, Enantiomers can be prepared by asymmetric synthesis, for example, see Jacques, et al, Enantiomers, racemes and solutions (Wiley Interscience, New York, 1981); principles of Asymmetric Synthesis (2)^nd Ed.Robert E.Gawley,Jeffrey Aube,Elsevier,Oxford,UK,2012)；Eliel,E.L.Stereochemistry of Carbon Compounds(McGraw-Hill,NY,1962)；Wilen,S.H.Tables of Resolving Agents and Optical Resolutions p.268(E.L.Eliel,Ed.,Univ.of Notre Dame Press,Notre Dame,IN 1972)；Chiral Separation Techniques:A Practical Approach(Subramanian,G.Ed.,Wiley-VCH Verlag GmbH&Co.KGaA,Weinheim,Germany,2007)。

The term "tautomer" or "tautomeric form" refers to structural isomers having different energies that can interconvert by a low energy barrier (low energy barrier). If tautomerism is possible (e.g., in solution), then the chemical equilibrium of the tautomer can be reached. For example, proton tautomers (also known as proton transfer tautomers) include interconversions by proton migration, such as keto-enol isomerization and imine-enamine isomerization.

"pharmaceutically acceptable" refers to those compounds, materials, compositions, and/or dosage forms which are, within the scope of sound medical judgment, suitable for use in contact with the tissues of patients without excessive toxicity, irritation, allergic response, or other problem or complication commensurate with a reasonable benefit/risk ratio, and which are effective for their intended use.

The term "prodrug", as used herein, represents a compound that is converted in vivo to a compound of formula (I) or (II). Thus, the device is provided withIs affected by hydrolysis of the prodrug in the blood or by enzymatic conversion to the parent structure in the blood or tissue. The prodrug compound of the invention can be ester, and in the prior invention, the ester can be used as the prodrug and comprises phenyl ester and aliphatic (C)_1-24) Esters, acyloxymethyl esters, carbonates, carbamates and amino acid esters. For example, a compound of the present invention contains a hydroxy group, i.e., it can be acylated to provide the compound in prodrug form. Other prodrug forms include phosphate esters, such as those obtained by phosphorylation of a hydroxyl group on the parent. For a complete discussion of prodrugs, reference may be made to the following: higuchi et al, Pro-drugs as Novel Delivery Systems, vol.14, a.c.s.symposium Series; roche et al, ed., Bioreversible Cariers in Drug Design, American Pharmaceutical Association and Pergamon Press, 1987; rautio et al, primers: Design and Clinical Applications, Nature Reviews Drug Discovery,2008,7,255-.

"metabolite" refers to the product of a particular compound or salt thereof obtained by metabolism in vivo. Metabolites of a compound can be identified by techniques well known in the art, and its activity can be characterized by assay methods as described herein. Such products may be obtained by administering the compound by oxidation, reduction, hydrolysis, amidation, deamidation, esterification, defatting, enzymatic cleavage, and the like. Accordingly, the present invention includes metabolites of compounds, including metabolites produced by contacting a compound of the present invention with a mammal for a sufficient period of time.

As used herein, "pharmaceutically acceptable salts" refer to organic and inorganic salts of the compounds of the present invention. Pharmaceutically acceptable salts are well known in the art, as are: berge et al, description of the scientific acceptable salts in detail in J. pharmaceutical Sciences,1977,66:1-19. Pharmaceutically acceptable non-toxic acidsSalts formed include, but are not limited to, salts of inorganic acids formed by reaction with amino groups such as hydrochlorides, hydrobromides, phosphates, sulfates, perchlorates, and salts of organic acids such as acetates, oxalates, maleates, tartrates, citrates, succinates, malonates, or by other methods described in the literature above such as ion exchange. Other pharmaceutically acceptable salts include adipates, alginates, ascorbates, aspartates, benzenesulfonates, benzoates, bisulfates, borates, butyrates, camphorates, camphorsulfonates, cyclopentylpropionates, digluconates, dodecylsulfates, ethanesulfonates, formates, fumarates, glucoheptonates, glycerophosphates, gluconates, hemisulfates, heptanoates, hexanoates, hydroiodides, 2-hydroxy-ethanesulfonates, lactobionates, lactates, laurates, malates, methanesulfonates, 2-naphthalenesulfonates, nicotinates, nitrates, oleates, palmitates, pamoates, pectinates, persulfates, 3-phenylpropionates, picrates, pivalates, propionates, stearates, thiocyanates, p-toluenesulfonate, undecanoate, valerate, and the like. Salts obtained with appropriate bases include alkali metals, alkaline earth metals, ammonium and N⁺(C_1-4Alkyl radical)₄A salt. The present invention also contemplates quaternary ammonium salts formed from compounds containing groups of N. Water-soluble or oil-soluble or dispersion products can be obtained by quaternization. Alkali or alkaline earth metal salts include sodium, lithium, potassium, calcium, magnesium, and the like. Pharmaceutically acceptable salts further include suitable, non-toxic ammonium, quaternary ammonium salts and amine cations resistant to formation of counterions, such as halides, hydroxides, carboxylates, sulfates, phosphates, nitrates, C_1-8Sulfonates and aromatic sulfonates.

"solvate" of the present invention refers to an association of one or more solvent molecules with a compound of the present invention. Solvents that form solvates include, but are not limited to, water, isopropanol, ethanol, methanol, dimethyl sulfoxide, ethyl acetate, acetic acid, ethanolamine, or mixtures thereof. The term "hydrate" refers to an association of solvent molecules that is water.

When the solvent is water, the term "hydrate" may be used. In one embodiment, a molecule of a compound of the present invention may be associated with a molecule of water, such as a monohydrate; in another embodiment, one molecule of the compound of the present invention may be associated with more than one molecule of water, such as a dihydrate, and in yet another embodiment, one molecule of the compound of the present invention may be associated with less than one molecule of water, such as a hemihydrate. It should be noted that the hydrates of the present invention retain the biological effectiveness of the compound in its non-hydrated form.

The term "therapeutically effective amount" or "therapeutically effective dose" as used herein refers to an amount of a compound of the invention that is capable of eliciting a biological or medical response (e.g., reducing or inhibiting enzyme or protein activity, or ameliorating symptoms, alleviating a disorder, slowing or delaying the progression of a disease, or preventing a disease, etc.) in a subject.

The invention relates to substituted (octahydropyrrolo [3, 4-c)]Pyrrol-2 (1H) -yl) phenyl methanones, pharmaceutically acceptable salts thereof, pharmaceutical compositions thereof and pharmaceutical formulations thereof having orexin receptor antagonistic activity, useful as orexin receptor antagonists, particularly as selective OX₁Receptor antagonists are useful in the prevention or treatment of diseases associated with orexin receptors, such as sleep disorders, psychiatric, neurological and neurodegenerative disorders, drug dependence, addiction, cognitive disorders, movement disorders, eating disorders, and the like.

Unless otherwise indicated, all suitable isotopic variations, stereoisomers, tautomers, solvates, metabolites, salts and pharmaceutically acceptable prodrugs of the compounds of the present invention are encompassed within the scope of the present invention.

The compounds of formula (I) or formula (II) may exist in different tautomeric forms and all such tautomers are included within the scope of the invention.

Nitroxides of the compounds of the present invention are also included within the scope of the present invention. The nitroxides of the compounds of the present invention may be prepared by oxidation of the corresponding nitrogen-containing basic species using a common oxidizing agent (e.g. hydrogen peroxide) in the presence of an acid such as acetic acid at elevated temperature, or by reaction with a peracid in a suitable solvent, for example peracetic acid in dichloromethane, ethyl acetate or methyl acetate, or 3-chloroperoxybenzoic acid in chloroform or dichloromethane.

In addition, when the compounds of the present invention form hydrates or solvates, they are also included in the scope of the present invention. Similarly, pharmaceutically acceptable salts of hydrates or solvates of the compounds of the invention are also included within the scope of the invention.

The compounds of formula (I) or formula (II) may be present in the form of a salt. In one embodiment, the salt refers to a pharmaceutically acceptable salt. The pharmaceutically acceptable salts of the present invention can be synthesized from the parent compound, basic or acidic moiety, by conventional chemical methods. In general, such salts can be prepared by reacting the free acid forms of these compounds with a stoichiometric amount of the appropriate base (e.g., Na, Ca, Mg, or K hydroxide, carbonate, bicarbonate, etc.), or by reacting the free base forms of these compounds with a stoichiometric amount of the appropriate acid. Such reactions are usually carried out in water or an organic solvent or a mixture of both. Generally, where appropriate, it is desirable to use a non-aqueous medium such as diethyl ether, ethyl acetate, ethanol, isopropanol or acetonitrile. In, for example, "Remington's Pharmaceutical Sciences", 20 th edition, Mack Publishing Company, Easton, Pa., (1985); and "handbook of pharmaceutically acceptable salts: properties, Selection and application (Handbook of Pharmaceutical Salts: Properties, Selection, and Use) ", Stahl and Wermuth (Wiley-VCH, Weinheim, Germany, 2002) may find some additional lists of suitable Salts.

The compounds of the invention are basic and therefore generally are capable of forming pharmaceutically acceptable acid addition salts by treatment with a suitable acid. Suitable acids include pharmaceutically acceptable inorganic acids and pharmaceutically acceptable organic acids. Representative pharmaceutically acceptable acid addition salts include the hydrochloride, hydrobromide, nitrate, methyl nitrate, sulfate, bisulfate, sulfamate, phosphate, acetate, glycolate, phenylacetate, propionate, butyrate, isobutyrate, valerate, maleate, hydroxymaleate, acrylate, fumarate, malate, tartrate, citrate, salicylate, para-aminosalicylate, glycolate, lactate, heptanoate, phthalate, oxalate, succinate, benzoate, o-acetoxybenzoate, chlorobenzoate, methylbenzoate, dinitrobenzoate, hydroxybenzoate, methoxybenzoate, mandelate, tannate, formate, stearate, ascorbate, palmitate, oleate, pyruvate, malate, tartrate, citrate, salicylate, maleate, tartrate, citrate, maleate, fumarate, maleate, tartrate, maleate, or salt of a compound, Pamoate, malonate, laurate, glutarate, glutamate, etonate, mesylate, hexanesulfonate, 2-hydroxyethanesulfonate, benzenesulfonate, sulfanilate, p-toluenesulfonate, and naphthalene-2-sulfonate, and the like.

Any formulae given herein are also intended to represent the non-isotopically enriched forms as well as the isotopically enriched forms of these compounds. Isotopically enriched compounds have the structure depicted by the formulae given herein, except that one or more atoms are replaced by an atom having a selected atomic mass or mass number. Exemplary isotopes that can be incorporated into compounds of the invention include isotopes of hydrogen, carbon, nitrogen, oxygen, phosphorus, sulfur, fluorine and chlorine, such as²H、³H、¹¹C、¹³C、¹⁴C、¹⁵N、¹⁷O、¹⁸O、¹⁸F、³¹P、³²P、³⁵S、³⁶Cl and¹²⁵I。

in another aspect, the compounds of the invention include isotopically enriched compounds as defined herein, e.g. wherein a radioisotope, e.g. is present³H、¹⁴C and¹⁸those compounds of F, or in which a non-radioactive isotope is present, e.g.²H and¹³C. the isotopically enriched compounds can be used for metabolic studies (use)¹⁴C) Reaction kinetics study (using, for example²H or³H) Detecting or imagingTechniques such as Positron Emission Tomography (PET) or Single Photon Emission Computed Tomography (SPECT) including measurement of drug or substrate tissue distribution, or may be used in radiotherapy of a patient.¹⁸F-enriched compounds are particularly desirable for PET or SPECT studies. Isotopically enriched compounds of formula (I) or formula (II) can be prepared by conventional techniques known to those skilled in the art or by the procedures and examples described in the present specification using a suitable isotopically labelled reagent in place of the original used unlabelled reagent.

In another aspect, the invention relates to intermediates for the preparation of compounds of formula (I) or formula (II).

In another aspect, the invention relates to methods for the preparation, isolation and purification of compounds of formula (I) or formula (II).

Pharmaceutical compositions, formulations and administration of the compounds of the invention

The invention provides a pharmaceutical composition, which comprises a compound shown in a formula (I) or a formula (II) or a stereoisomer, a tautomer, a nitrogen oxide, a solvate, a metabolite, a pharmaceutically acceptable salt or a prodrug of the compound shown in the formula (I) or the formula (II). The pharmaceutical composition further comprises at least one pharmaceutically acceptable carrier, adjuvant or excipient, and optionally, other therapeutic and/or prophylactic ingredients.

Suitable carriers, adjuvants and excipients are well known to those skilled in the art and are described in detail, for example, in Ansel h.c.et al, Ansel's Pharmaceutical Dosage Forms and Drug Delivery Systems (2004) Lippincott, Williams & Wilkins, philidelphia; gennaroa. r.et al, Remington: the Science and Practice of Pharmacy (2000) Lippincott, Williams & Wilkins, Philadelphia; and Rowe R.C., Handbook of Pharmaceutical Excipients (2005) Pharmaceutical Press, Chicago.

As used herein, "pharmaceutically acceptable excipient" means a pharmaceutically acceptable material, mixture or vehicle that is compatible with the dosage form or pharmaceutical composition to be administered. Each excipient, when mixed, must be compatible with the other ingredients of the pharmaceutical composition in order to avoid interactions that would substantially reduce the efficacy of the compounds of the invention when administered to a patient and interactions that would result in a pharmaceutical composition that is not pharmaceutically acceptable. Furthermore, each excipient must be pharmaceutically acceptable, e.g., of sufficiently high purity.

Suitable pharmaceutically acceptable excipients will vary depending on the particular dosage form selected. In addition, pharmaceutically acceptable excipients may be selected for their specific function in the composition. For example, certain pharmaceutically acceptable excipients may be selected to aid in the production of a uniform dosage form. Certain pharmaceutically acceptable excipients may be selected to aid in the production of stable dosage forms. Certain pharmaceutically acceptable excipients may be selected to facilitate carrying or transporting a compound of the invention from one organ or portion of the body to another organ or portion of the body when administered to a patient. Certain pharmaceutically acceptable excipients may be selected that enhance patient compliance.

Suitable pharmaceutically acceptable excipients include the following types of excipients: diluents, fillers, binders, disintegrants, lubricants, glidants, granulating agents, coating agents, wetting agents, solvents, co-solvents, suspending agents, emulsifiers, sweeteners, flavoring agents, taste masking agents, colorants, anti-caking agents, humectants, chelating agents, plasticizers, viscosity increasing agents, antioxidants, preservatives, stabilizers, surfactants and buffers. One skilled in the art will recognize that certain pharmaceutically acceptable excipients may provide more than one function, and provide alternative functions, depending on how many such excipients are present in the formulation and which other excipients are present in the formulation.

The skilled person is knowledgeable and skilled in the art to enable them to select suitable amounts of suitable pharmaceutically acceptable excipients for use in the present invention. Furthermore, there is a large amount of resources available to the skilled person, who describes pharmaceutically acceptable excipients and is used to select suitable pharmaceutically acceptable excipients. Examples include Remington's Pharmaceutical Sciences (Mack Publishing Company), The Handbook of Pharmaceutical Additives (Gower Publishing Limited), and The Handbook of Pharmaceutical Excipients (The American Pharmaceutical Association and The Pharmaceutical Press).

Various carriers for formulating pharmaceutically acceptable compositions, and well known techniques for their preparation, are disclosed in Remington, The Science and Practice of Pharmacy,21st edition,2005, ed.D.B.Troy, Lippincott Williams & Wilkins, Philadelphia, and Encyclopedia of Pharmaceutical Technology, eds.J.Swarbrick and J.C.Boylan, 1988. Annu 1999, Marcel Dekker, New York, The contents of each of which are incorporated herein by reference. Except insofar as any conventional carrier is incompatible with the compounds of the invention, such as by producing any undesirable biological effect or interacting in a deleterious manner with any other ingredient in a pharmaceutically acceptable composition, its use is contemplated as falling within the scope of the present invention.

The compounds of the present invention are generally formulated in a dosage form suitable for administration to a patient by a desired route. For example, dosage forms include those suitable for the following routes of administration: (1) oral administration, such as tablets, capsules, caplets, pills, troches, powders, syrups, elixirs, suspensions, solutions, emulsions, sachets and cachets; (2) parenteral administration, such as sterile solutions, suspensions, and reconstituted powders; (3) transdermal administration, such as transdermal patches; (4) rectal administration, e.g., suppositories; (5) inhalation, such as aerosols, solutions, and dry powders; and (6) topical administration, such as creams, ointments, lotions, solutions, pastes, sprays, foams and gels.

It will also be appreciated that certain compounds of the invention may be present in free form for use in therapy or, if appropriate, in the form of a pharmaceutically acceptable derivative thereof. Some non-limiting embodiments of pharmaceutically acceptable derivatives include pharmaceutically acceptable prodrugs, salts, esters, salts of such esters, or any additional adduct or derivative that upon administration to a patient in need thereof provides, directly or indirectly, a compound of the present invention or a metabolite or residue thereof.

In one embodiment, the compounds of the present invention may be formulated in oral dosage forms. In another embodiment, the compounds of the present invention may be formulated in an inhalation dosage form. In another embodiment, the compounds of the present invention may be formulated for nasal administration. In yet another embodiment, the compounds of the present invention may be formulated for transdermal administration. In yet another embodiment, the compounds of the present invention may be formulated for topical administration.

The pharmaceutical compositions provided by the present invention may be provided as compressed tablets, milled tablets, chewable lozenges, fast-dissolving tablets, double-compressed tablets, or enteric-coated, sugar-coated or film-coated tablets. Enteric coated tablets are compressed tablets coated with a substance that is resistant to the action of gastric acid but dissolves or disintegrates in the intestine, thereby preventing the active ingredient from contacting the acidic environment of the stomach. Enteric coatings include, but are not limited to, fatty acids, fats, phenyl salicylate, waxes, shellac, ammoniated shellac, and cellulose acetate phthalate. Sugar-coated tablets are compressed tablets surrounded by a sugar coating, which can help to mask unpleasant tastes or odors and prevent oxidation of the tablet. Film-coated tablets are compressed tablets covered with a thin layer or film of a water-soluble substance. Film coatings include, but are not limited to, hydroxyethyl cellulose, sodium carboxymethyl cellulose, polyethylene glycol 4000, and cellulose acetate phthalate. Film coatings are endowed with the same general characteristics as sugar coatings. A tabletted tablet is a compressed tablet prepared over more than one compression cycle, including a multi-layer tablet, and a press-coated or dry-coated tablet.

Tablet dosage forms may be prepared from the active ingredient in powder, crystalline or granular form, alone or in combination with one or more carriers or excipients described herein, including binders, disintegrants, controlled release polymers, lubricants, diluents and/or colorants. Flavoring and sweetening agents are particularly useful in forming chewable tablets and lozenges.

The pharmaceutical composition provided by the present invention may be provided in soft or hard capsules, which may be prepared from gelatin, methylcellulose, starch or calcium alginate. The hard gelatin capsules, also known as Dry Fill Capsules (DFC), consist of two segments, one inserted into the other, thus completely encapsulating the active ingredient. Soft Elastic Capsules (SEC) are soft, spherical shells, such as gelatin shells, which are plasticized by the addition of glycerol, sorbitol or similar polyols. The soft gelatin shell may contain a preservative to prevent microbial growth. Suitable preservatives are those as described herein, including methyl and propyl parabens, and sorbic acid. The liquid, semi-solid and solid dosage forms provided by the present invention may be encapsulated in a capsule. Suitable liquid and semi-solid dosage forms include solutions and suspensions in propylene carbonate, vegetable oils or triglycerides. Capsules containing such solutions may be as described in U.S. patent nos.4,328,245; 4,409,239 and 4,410,545. The capsules may also be coated as known to those skilled in the art to improve or maintain dissolution of the active ingredient.

The pharmaceutical compositions provided herein may be provided in liquid and semi-solid dosage forms, including emulsions, solutions, suspensions, elixirs and syrups. Emulsions are two-phase systems in which one liquid is dispersed throughout another in the form of globules, which can be either oil-in-water or water-in-oil. Emulsions may include pharmaceutically acceptable non-aqueous liquids and solvents, emulsifiers and preservatives. Suspensions may include a pharmaceutically acceptable suspending agent and a preservative. The aqueous alcoholic solution may comprise pharmaceutically acceptable acetals, such as di (lower alkyl) acetals of lower alkyl aldehydes, e.g. acetaldehyde diethyl acetal; and water-soluble solvents having one or more hydroxyl groups, such as propylene glycol and ethanol. Elixirs are clear, sweetened, hydroalcoholic solutions. Syrups are concentrated aqueous solutions of sugars, such as sucrose, and may also contain preservatives. For liquid dosage forms, for example, a solution in polyethylene glycol may be diluted with a sufficient amount of a pharmaceutically acceptable liquid carrier, such as water, for precise and convenient administration.

The pharmaceutical compositions provided herein may be formulated in any dosage form suitable for administration to a patient by inhalation, such as a dry powder, aerosol, suspension or solution composition. In one embodiment, the disclosed pharmaceutical compositions may be formulated in a dosage form suitable for inhalation administration to a patient as a dry powder. In yet another embodiment, the disclosed pharmaceutical compositions may be formulated in a dosage form suitable for inhalation administration to a patient via a nebulizer. Delivered to the lungs by inhalationDry powder compositions generally comprise a finely powdered compound disclosed herein and one or more finely powdered pharmaceutically acceptable excipients. Pharmaceutically acceptable excipients that are particularly suitable for use as dry powders are known to those skilled in the art and include lactose, starch, mannitol, and mono-, di-and polysaccharides. Fine powders may be prepared, for example, by micronization and milling. Generally, the size-reduced (e.g., micronized) compound may pass through a D of about 1 to 10 microns₅₀Values (e.g., measured by laser diffraction).

Pharmaceutical compositions suitable for transdermal administration may be prepared as discrete patches intended to remain in intimate contact with the epidermis of the patient for an extended period of time. For example, the active ingredient may be delivered from a patch agent by iontophoresis, as generally described in Pharmaceutical Research,3(6),318 (1986).

Pharmaceutical compositions suitable for topical administration may be formulated as ointments, creams, suspensions, lotions, powders, solutions, pastes, gels, sprays, aerosols or oils. For example, ointments, creams and gels may be formulated with a water or oil base, and suitable thickeners and/or gelling agents and/or solvents. Such bases may include, water, and/or oils such as liquid paraffin and vegetable oils (e.g., peanut oil or castor oil), or solvents such as polyethylene glycol. Thickeners and gelling agents used according to the nature of the base include soft paraffin, aluminium stearate, cetostearyl alcohol, polyethylene glycol, lanolin, beeswax, carbopol and cellulose derivatives, and/or glyceryl monostearate and/or non-ionic emulsifiers.

The compounds of the invention may also be conjugated to soluble polymers as targeted drug carriers. Such polymers include polyvinylpyrrolidone, pyran copolymer, polyhydroxypropylmethacrylamide-phenol, polyhydroxyethylaspartamidephenol or polyoxyethylene polylysine substituted with palmitoyl residues. In addition, the disclosed compounds may be combined with a class of biodegradable polymers used in achieving controlled release of a drug, such as polylactic acid, polyepsilon caprolactone, polyhydroxy butyric acid, polyorthoesters, polyacetals, polydihydropyrans, polycyanoacrylates, and crosslinked or amphiphilic block copolymers of hydrogels.

The pharmaceutical compositions provided by the present invention may be administered parenterally by injection, infusion or implantation for local or systemic administration. Parenteral administration as used herein includes intravenous, intraarterial, intraperitoneal, intrathecal, intraventricular, intraurethral, intrasternal, intracranial, intramuscular, intrasynovial and subcutaneous administration.

The pharmaceutical compositions provided herein can be formulated in any dosage form suitable for parenteral administration, including solutions, suspensions, emulsions, micelles, liposomes, microspheres, nanosystems and solid forms suitable for solution or suspension in a liquid prior to injection. Such dosage forms may be prepared according to conventional methods known to those skilled in The art of pharmaceutical Science (see Remington: The Science and Practice of Pharmacy, supra).

Pharmaceutical compositions intended for parenteral administration may include one or more pharmaceutically acceptable carriers and excipients, including, but not limited to, aqueous vehicles, water-miscible vehicles, non-aqueous vehicles, antimicrobial agents or preservatives to inhibit microbial growth, stabilizers, solubility enhancers, isotonic agents, buffers, antioxidants, local anesthetics, suspending and dispersing agents, wetting or emulsifying agents, complexing agents, sequestering or chelating agents, cryoprotectants, thickening agents, pH adjusting agents, and inert gases.

The pharmaceutical compositions provided by the present invention may be formulated into immediate or modified release dosage forms, including delayed-, sustained-, pulsed-, controlled-, targeted-, and programmed release forms.

The pharmaceutical compositions provided herein may be formulated for single or multiple dose administration. The single dose formulations are packaged in ampoules, vials or syringes. The multi-dose parenteral formulation must contain a bacteriostatic or fungistatic concentration of the antimicrobial agent. All parenteral formulations must be sterile, as is known and practiced in the art.

The pharmaceutical compositions provided by the present invention may be co-formulated with other active ingredients that do not impair the intended therapeutic effect, or with substances that supplement the intended effect.

In one embodiment, the treatment methods of the present invention comprise administering to a patient in need thereof a safe and effective amount of a compound of the present invention or a pharmaceutical composition comprising a compound of the present invention. Various embodiments of the present invention encompass the treatment of the diseases mentioned herein by administering to a patient in need thereof a safe and effective amount of a compound of the present invention or a pharmaceutical composition comprising a compound of the present invention.

In one embodiment, a compound of the invention or a pharmaceutical composition comprising a compound of the invention may be administered by any suitable route of administration, including systemic and topical administration. Systemic administration includes oral, parenteral, transdermal and rectal administration. Typical parenteral administration refers to administration by injection or infusion, including intravenous, intramuscular, and subcutaneous injection or infusion. Topical administration includes application to the skin and intraocular, otic, intravaginal, inhalation, and intranasal administration. In one embodiment, a compound of the invention or a pharmaceutical composition comprising a compound of the invention may be administered orally. In another embodiment, a compound of the invention or a pharmaceutical composition comprising a compound of the invention may be administered by inhalation. In yet another embodiment, the compound of the invention or a composition comprising the compound of the invention may be administered intranasally.

In one embodiment, a compound of the invention or a pharmaceutical composition comprising a compound of the invention may be administered once or several times at different time intervals over a specified period of time according to a dosing regimen. For example, once, twice, three times or four times daily. In one embodiment, the administration is once daily. In yet another embodiment, the administration is twice daily. The administration may be carried out until the desired therapeutic effect is achieved or the desired therapeutic effect is maintained indefinitely. Suitable dosing regimens for the compounds of the invention or pharmaceutical compositions comprising the compounds of the invention depend on the pharmacokinetic properties of the compound, such as absorption, distribution and half-life, which can be determined by the skilled person. In addition, the appropriate dosage regimen, including the duration of the regimen, of the compound of the invention or of the pharmaceutical composition containing the compound of the invention depends on the condition being treated, the severity of the condition being treated, the age and physical condition of the patient being treated, the medical history of the patient being treated, the nature of concurrent therapy, the desired therapeutic effect, and other factors within the knowledge and experience of the skilled artisan. Such a skilled artisan will also appreciate that adjustments to the subject's response to the dosage regimen, or the need for changes in the subject's patient over time, may be required.

The compounds of the present invention may be administered simultaneously, or before or after, one or more other therapeutic agents. The compounds of the invention may be administered separately from the other therapeutic agents, by the same or different routes of administration, or together with them in pharmaceutical compositions.

The compounds of the present invention may be used in combination with sedatives, hypnotics, anxiolytics, antipsychotics, anxiolytics, cyclic pyrrolidones, imidazopyridines, pyrazolopyrimidines, weakly tranquilizers, melatonin agonists and antagonists, melatonin-ergetics, benzodiazepines, barbiturates, 5HT-2 antagonists and the like, for example: ardizolam, diallabamectin, spironaperone, alprazolam, amitriptyline, amobarbital, phenoxipam, tylidine, brotizolam, bupropion, buspirone, butabarbital, captopril, carpourea, carboxaldehyde, betaine chloroaldehyde, chloral hydrate, chlordiazepoxide, clomipramine, clonazepam, cloperazone, chlordiazepoxide, clozapine, ciprofloxacin, despramine, cycloheptapylquinol, diazepam, chlorasalamide, dipropanoic acid, chlorphenamine, doxylamine, estamine, estazolam, chloroethylpentenol, mebendazole, fenoban, flunitrazepam, fluvoxamine, fenzopyr, diazepam, mephostylamine, meplizine, halazepam, oxazipam, hydroxyzine, promethazine, lithium, chlordiazepoxide, mepiridine, meprobamate, Ambam, hypnone, midazolam, nefazodone, nisolone, diazepam, nortriptyline, nordroxydiazepam, paraldehyde, paroxetine, pentobarbital, piperapine, perphenazine, phenelzine, phenobarbital, ciprofloxacin, promethazine, propofol, protiline, tetrafluorothiodiazepam, relchlorazepam, rolipram, secobarbital, sertraline, sulproone, temazepam, thioridazine, tracarbazolyl, tranylcypromine, trazodone, triazoldiazepam, trapazon, trimethoxyphenylacetamide, trichloroethylammonium, trifluoperazine, trimethophenamorph, trimethoprim, urazepam, venlafaxine, zaleplon, zolazepam, zolpidem, and salts and combinations thereof, and the like, alternatively, the compounds of the invention may be administered in combination with physical means such as light therapy or electrical stimulation.

In addition, the compounds of the present invention may be administered in the form of a prodrug. In the present invention, a "prodrug" of a compound of the present invention is a functional derivative that, when administered to a patient, is ultimately released in vivo from the compound of the present invention. When administering the compounds of the present invention in prodrug form, one skilled in the art can practice one or more of the following: (a) altering the in vivo onset time of the compound; (b) altering the duration of action of the compound in vivo; (c) altering the in vivo delivery or distribution of the compound; (d) altering the in vivo solubility of the compound; and (e) overcoming side effects or other difficulties faced by the compounds. Typical functional derivatives useful for preparing prodrugs comprise variants of the compounds which are cleaved in vivo either chemically or enzymatically. These variants, which involve the preparation of phosphates, amides, esters, thioesters, carbonates and carbamates, are well known to those skilled in the art.

Application of compound and pharmaceutical composition of the invention

The compounds and pharmaceutical compositions described herein are useful as orexin receptor antagonists, particularly as selective OX₁Receptor antagonists, which are effective in preventing or treating diseases associated with orexin receptors, are useful for the preparation of pharmaceuticals for antagonizing orexin receptors.

The diseases related to orexin receptors may be selected from all types of sleep disorders, all types of psychiatric, neurological and neurodegenerative disorders, all types of stress-related syndromes, all types of addiction (especially the use, abuse, seeking and recovery of psychoactive substances), all types of cognitive dysfunction in healthy populations and in psychiatric and neurological patients, all types of eating or drinking disorders, etc.

In one embodiment, the condition associated with an orexin receptor comprises sleep disorders, depression, anxiety disorders, panic disorders, obsessive-compulsive disorders, affective neuropathies, depressive neuropathies, anxiety neuropathies, mood disorders, panic attack disorders, behavioral disorders, mood disorders, post-traumatic stress disorders, sexual dysfunction, psychosis, schizophrenia, manic depression, delirium, dementia, drug dependence, addiction, cognitive disorders, alzheimer's disease, parkinson's disease, movement disorders, eating disorders, headache, migraine, pain, digestive system disorders, epilepsy, inflammation, cardiovascular disorders, diabetes, metabolic disorders, immune-related disorders, endocrine-related disorders or hypertension.

In one embodiment, the orexin receptor associated disease may be selected from sleep disorders, which include all types of insomnia, narcolepsy and other excessive sleepiness disorders, parasomnia, sleep-related dystonia, restless leg syndrome, sleep apnea syndrome, circadian rhythm disorder, jet lag syndrome, shift work syndrome, insomnia associated with delayed or advanced sleep phase syndrome or psychiatric disorders, and the like.

In one embodiment, the condition associated with an orexin receptor may be selected from psychiatric, neurological and neurodegenerative disorders including depression, anxiety, panic, obsessive compulsive disorder, affective neuropathy, depressive neuropathy, anxiety neuropathy, mood disorders, panic attack disorders, post-traumatic stress disorders, sexual dysfunction, psychosis, parkinson's disease, dementia or mental retardation, and the like.

In one embodiment, the orexin receptor-associated disorder may be selected from cognitive dysfunction, which includes all types of attention, learning and memory decline of transient or chronic episodes in the normal, healthy, young, adult or elderly population, or all types of attention, learning and memory decline of transient or chronic episodes in patients with psychiatric, neurological, cardiovascular and immune system disorders, and the like.

It will be appreciated that the compounds of the invention are particularly useful for the treatment of any of these environmentally regulated disorders or diseases in situations where certain environmental conditions such as stress or fear (where stress may be of social origin such as social stress or of physiological origin such as physiological stress, including stress resulting from fear) promote or accelerate any of the disorders or diseases previously described.

In addition to being beneficial for human therapy, the compounds and pharmaceutical compositions of the present invention may also find application in veterinary therapy for pets, animals of the introduced species and mammals in farm animals. Examples of other animals include horses, dogs, and cats. Herein, the compound of the present invention includes pharmaceutically acceptable derivatives thereof.

General Synthesis of Compounds of the invention

To illustrate the invention, the following examples are set forth. It is to be understood that the invention is not limited to these embodiments, but is provided as a means of practicing the invention.

In general, the compounds of the invention may be prepared by the methods described herein, wherein the substituents are as defined in formula (I) or formula (II), unless otherwise indicated. The following reaction schemes and examples serve to further illustrate the context of the invention.

Those skilled in the art will recognize that: the chemical reactions described herein may be used to suitably prepare a number of other compounds of the invention, and other methods for preparing the compounds of the invention are considered to be within the scope of the invention. For example, the synthesis of those non-exemplified compounds according to the present invention can be successfully accomplished by those skilled in the art by modification, such as appropriate protection of interfering groups, by the use of other known reagents in addition to those described herein, or by some routine modification of reaction conditions. In addition, the reactions disclosed herein or known reaction conditions are also recognized as being applicable to the preparation of other compounds of the present invention.

The examples described below, unless otherwise indicated, are all temperatures set forth in degrees Celsius. Reagents were purchased from commercial suppliers such as Aldrich Chemical Company, Arco Chemical Company and Alfa Chemical Company and were used without further purification unless otherwise indicated. General reagents were purchased from Shantou Wen Long chemical reagent factory, Guangdong Guanghua chemical reagent factory, Guangzhou chemical reagent factory, Tianjin Haojian Yunyu chemical Co., Ltd, Tianjin Shucheng chemical reagent factory, Wuhan Xin Huayuan scientific and technological development Co., Ltd, Qingdao Tenglong chemical reagent Co., Ltd, and Qingdao Kaolingyi factory.

The anhydrous tetrahydrofuran, dioxane, toluene and ether are obtained through reflux drying of metal sodium. The anhydrous dichloromethane and chloroform are obtained by calcium hydride reflux drying. Ethyl acetate, petroleum ether, N-hexane, N, N-dimethylacetamide and N, N-dimethylformamide were used as they were previously dried over anhydrous sodium sulfate.

The following reactions are generally carried out under positive pressure of nitrogen or argon or by sleeving a dry tube over an anhydrous solvent (unless otherwise indicated), the reaction vial being stoppered with a suitable rubber stopper and the substrate being injected by syringe. The glassware was dried.

The column chromatography is performed using a silica gel column. Silica gel (300 and 400 meshes) was purchased from Qingdao oceanic chemical plants.

¹H NMR spectra were recorded using a Bruker 400MHz or 600MHz NMR spectrometer.¹H NMR Spectrum in CDC1₃、DMSO-d₆、CD₃OD or acetone-d₆TMS (0ppm) or chloroform (7.26ppm) was used as a reference standard for the solvent (in ppm). When multiple peaks occur, the following abbreviations will be used: s (singleton), d (doublet), t (triplet), m (multiplet), br (broad), dd (doublet of doublets), dt (doublet of doublets), and dt (doublet of triplets). Coupling constants are expressed in hertz (Hz).

The conditions for determining low resolution Mass Spectrometry (MS) data were: agilent 6120 quaternary stageRod HPLC-MS (column model: Zorbax SB-C18,2.1X 30mm,3.5 microns, 6min, flow rate 0.6 mL/min. mobile phase 5% -95% (CH with 0.1% formic acid)₃CN) in (H containing 0.1% formic acid)₂O) by electrospray ionization (ESI) at 210nm/254nm, with UV detection.

Pure compounds were detected by UV at 210nm/254nm using Agilent 1260 pre-HPLC or Calesep pump 250 pre-HPLC (column model: NOVASEP 50/80mm DAC).

The following acronyms are used throughout the invention:

boc tert-butyloxycarbonyl group

CH₂Cl₂DCM dichloromethane

Cs₂CO₃Cesium carbonate

CDC1₃Deuterated chloroform

CuI cuprous iodide

DMF N, N-dimethylformamide

DMSO dimethyl sulfoxide

Et₃N, TEA Triethylamine

EtOAc, EA ethyl acetate

EtOH ethanol

g

h hours

MeCN、CH₃CN acetonitrile

Na₂CO₃Sodium carbonate

NaOH sodium hydroxide

Na₂SO₄Sodium sulfate

MgSO₄Magnesium sulfate

mL, mL

PE Petroleum ether (60-90 deg.C)

RT, RT, r.t. Room temperature

The following synthetic schemes describe the procedures for preparing the compounds of the present invention. Unless otherwise indicated, R¹、R²、R³、R⁴、R⁵、R⁶、R⁷、R⁸And R⁹Having the definitions as described in the present invention.

Synthesis scheme 1

Compound 9 of the present invention can be prepared by the general synthetic methods described in synthetic scheme 1 and detailed in the specific examples: firstly, 1, 6-naphthyridin-5 (6H) -ketone 1 and a chlorinated reagent are heated to obtain a compound 2, the compound 2 and 2-Boc-hexahydropyrrolo [3,4-c ] pyrrole are heated to obtain a compound 3 under an alkaline condition, the compound 3 is functionalized to obtain a compound 4 containing different substituent groups, and the compound 4 is subjected to an acidic condition to obtain an intermediate compound 5.

Optionally substituted o-iodobenzoic acid 6 and 2H-1,2, 3-triazole are reacted in the presence of proper alkali and under a heating condition through a catalyst (such as CuI) to obtain a compound 7, then the compound 7 and a chlorinated reagent are heated to obtain a compound 8, and finally the compound 8 and an intermediate compound 5 are subjected to an alkaline condition to obtain a target compound 9.

The compounds, pharmaceutical compositions and uses thereof provided by the present invention are further illustrated below in connection with the examples.

Examples

EXAMPLE 1 Synthesis of (5- (1, 6-naphthyridin-5-yl) hexahydropyrrolo [3,4-c ] pyrrol-2 (1H) -yl) (5-methyl-2- (2H-1,2, 3-triazol-2-yl) phenyl) methanone

Step 1) Synthesis of 5-chloro-1, 6-naphthyridine

1, 6-naphthyridin-5 (6H) -one (3.00g,20.53mmol) and phosphorus oxychloride (40mL) were added to a 100mL reaction flask and the reaction was warmed to 100 ℃ for 24 hours. The reaction was stopped, the reaction was cooled to room temperature, excess phosphorus oxychloride was removed by distillation under the reduced pressure, the remaining solid was quenched with ice saturated sodium bicarbonate solution (80mL), and the aqueous phase was extracted with dichloromethane (30 mL. times.3). The combined organic phases were dried over anhydrous sodium sulfate, filtered, the filtrate was dried under reduced pressure and purified by silica gel column chromatography (petroleum ether/ethyl acetate (v/v) ═ 1/1) to give the title compound (white solid, 3.08g, 91.20%).

MS(ESI,pos.ion)m/z:165.15[M+H]⁺；

¹H NMR(CDCl₃,400MHz)δ(ppm):9.15(dd,J＝4.2,1.5Hz,1H),8.71～8.60(m,1H),8.53(d,J＝5.9Hz,1H),7.90(d,J＝5.8Hz,1H),7.64(dd,J＝8.5,4.3Hz,1H).

Step 2)5- (1, 6-naphthyridin-5-yl) hexahydropyrrolo [3, 4-c)]Synthesis of pyrrole-2 (1H) -carboxylic acid tert-butyl ester Become into

5-chloro-1, 6-naphthyridine (0.93g,5.65mmol), t-butyl hexahydropyrrolo [3,4-c ] pyrrole-2 (1H) -carboxylate (1.00g,4.71mmol), tris (dibenzylideneacetone) dipalladium (0.43g,0.47mmol), 2-dicyclohexylphosphonium-2, 4, 6-triisopropylbiphenyl (0.46g,0.94mmol), sodium tert-butoxide (1.40g,14.1mmol) and toluene (20mL) were added in this order to a 100mL single-neck flask, and the reaction was warmed to 120 ℃ under nitrogen for 36 hours. The reaction was stopped, and the reaction solution was distilled under reduced pressure to remove the solvent and then purified by silica gel column chromatography (petroleum ether/ethyl acetate (v/v) ═ 1/1) to give the title compound (pale yellow liquid, 1.15g, 71.7%).

MS(ESI,pos.ion)m/z:341.40[M+H]⁺；

¹H NMR(CDCl₃,600MHz)δ(ppm):8.88(dd,J＝4.1,1.2Hz,1H),8.46(d,J＝8.5Hz,1H),8.19(d,J＝5.8Hz,1H),7.30(dd,J＝8.6,4.2Hz,1H),7.24(d,J＝5.8Hz,1H),4.05(dd,J＝10.9,7.1Hz,2H),3.78～3.70(m,2H),3.64(d,J＝4.6Hz,2H),3.40(d,J＝9.8Hz,1H),3.32(d,J＝8.0Hz,1H),3.02～2.96(m,2H),1.45(s,9H).

Step 3)5- (hexahydropyrrolo [3, 4-c)]Synthesis of pyrrol-2 (1H) -yl) -1, 6-naphthyridines

Tert-butyl 5- (1, 6-naphthyridin-5-yl) hexahydropyrrolo [3,4-c ] pyrrole-2 (1H) -carboxylate (1.10g,3.23mmol) was dissolved in dichloromethane (10mL), and a solution of hydrogen chloride in ethyl acetate (10mL) was added with stirring at room temperature to react at room temperature for 2 hours. The reaction evaporated off the solvent to dryness to give the title compound (pale yellow solid, 0.88g, 98.4%).

MS(ESI,pos.ion)m/z:241.30[M+H]⁺；

¹H NMR(D₂O,400MHz,)δ(ppm):9.39(d,J＝8.8Hz,1H),9.21(d,J＝5.1Hz,1H),8.06(d,J＝4.9Hz,1H),8.04(d,J＝3.3Hz,1H),7.44(d,J＝7.2Hz,1H),4.53(dd,J＝11.7,7.1Hz,2H),4.23(dd,J＝11.9,3.6Hz,2H),3.80(dd,J＝12.3,7.0Hz,2H),3.64～3.54(m,2H),3.49(dd,J＝12.4,4.9Hz,2H).

Step 4) synthesis of 5-methyl-2- (2H-1,2, 3-triazole-2-yl) benzoic acid

2H-1,2, 3-triazole (3.45g,50mmol), 2-iodo-5-methylbenzoic acid (5.24g,20mmol), cesium carbonate (11.72g,36mmol), trans-N, N' -dimethyl-1, 2-cyclohexanediamine (0.51g,3.6mmol), cuprous iodide (0.38g,2mmol) and N, N-dimethylformamide (30mL) were sequentially added to a 100mL single-neck round-bottom flask, and the reaction solution was gradually heated to 100 ℃ for 4 hours under nitrogen protection. The reaction was stopped, cooled, and the reaction solution was diluted with water (60mL) and extracted with ethyl acetate (200 mL. times.2). The aqueous layer was acidified with concentrated hydrochloric acid to pH 1 to 2, followed by extraction with ethyl acetate (200mL × 2), and the resulting organic layer was dried over anhydrous sodium sulfate, filtered, and the filtrate was spin-dried under reduced pressure and purified by column chromatography (dichloromethane/methanol (v/v) ═ 50/1) to give the title compound (yellow solid, 2.76g, 68%).

MS(ESI,neg.ion)m/z:202.1[M-H]^-；

¹H NMR(CD₃OD,600MHz)δ(ppm):7.88(s,2H),7.66(d,1H),7.59(d,J＝8.2Hz,1H),7.50～7.48(dd,J＝8.1Hz,1.1Hz,1H),2.45(s,3H)；

¹³C NMR(CD₃OD,151MHz)δ(ppm):169.8,140.7,137.5,136.7,133.5,131.5,129.3,126.0,21.0.

Step 5) synthesis of 5-methyl-2- (2H-1,2, 3-triazole-2-yl) benzoyl chloride

5-methyl-2- (2H-1,2, 3-triazol-2-yl) benzoic acid (2.03g,10mmol) was added to a 100mL single neck round bottom flask, dissolved in anhydrous dichloromethane (20mL), and thionyl chloride (15mL,200mmol) and pyridine (0.15mL,2mmol) were added slowly. And gradually heating the reaction solution to reflux, stopping the reaction after reacting for 3 hours, cooling, slowly evaporating the solvent under reduced pressure, and directly entering the next step to obtain the product.

Step 6) (5- (1, 6-naphthyridin-5-yl) hexahydropyrrolo [3, 4-c)]Pyrrole-2 (1H) -yl) (5-methyl-2- Synthesis of (2H-1,2, 3-triazole-2-yl) phenyl) methanone

5- (hexahydropyrrolo [3,4-c ] pyrrol-2 (1H) -yl) -1, 6-naphthyridine (0.40g,1.45mmol), triethylamine (0.58g,5.78mmol) and dichloromethane (20mL) were added to a 100mL single-neck flask, and after stirring at 0 ℃ for 10 minutes, a solution of 5-methyl-2- (2H-1,2, 3-triazol-2-yl) benzoyl chloride (0.48g,2.17mmol) in dichloromethane (10mL) was slowly added dropwise. The reaction mixture was further stirred at 0 ℃ for 30 minutes and then allowed to react at room temperature. After 12 hours of the reaction, the solvent was evaporated under reduced pressure, the remaining solid was dissolved in dichloromethane (30mL), and then washed with water (20mL) and saturated brine (20mL) in that order, and the organic layer was directly subjected to silica gel column chromatography (petroleum ether/ethyl acetate (v/v) ═ 1/2) to give the title compound (pale yellow viscous substance, 0.45g, 73.15%).

MS(ESI,pos.ion)m/z:426.10[M+H]⁺；

¹H NMR(CDCl₃,600MHz)δ(ppm):8.91(dd,J＝4.1,1.2Hz,1H),8.45(d,J＝8.5Hz,1H),8.22(d,J＝5.8Hz,1H),7.83(d,J＝8.3Hz,1H),7.74(s,2H),7.36～7.29(m,2H),7.28(d,J＝5.9Hz,1H),7.24(s,1H),4.08(dd,J＝10.7,7.5Hz,1H),3.95(dd,J＝10.8,7.1Hz,1H),3.88(dd,J＝12.6,7.6Hz,1H),3.80(dd,J＝10.8,5.3Hz,1H),3.73(dd,J＝12.6,4.0Hz,1H),3.68(dd,J＝10.7,3.6Hz,1H),3.39(s,1H),3.11～2.91(m,3H),2.40(s,3H)；

¹³C NMR(CDCl₃,150MHz)δ(ppm):168.4,157.3,153.3,152.9,144.9,138.6,135.8,135.3,134.4,133.6,130.7,129.7,128.3,122.2,119.5,115.0,113.1,51.6,49.6,41.1,21.0.

Example 2 Synthesis of (5- (1, 6-naphthyridin-5-yl) hexahydropyrrolo [3,4-c ] pyrrol-2 (1H) -yl) (2- (2H-1,2, 3-triazol-2-yl) phenyl) methanone

Step 1) synthesis of 2- (2H-1,2, 3-triazole-2-yl) benzoic acid

The title compound was prepared as described in example 1, step 4 by reacting 2H-1,2, 3-triazole (0.7g,10.08mmol), 2-iodobenzoic acid (1g,4.03mmol), cesium carbonate (2.36g,7.2mmol), trans-N, N' -dimethyl-1, 2-cyclohexanediamine (0.103g,0.752mmol) and cuprous iodide (0.077g,0.403mmol) in N, N-dimethylformamide (18mL) and purifying the crude by silica gel column chromatography (dichloromethane/methanol (v/v) ═ 30/1) to give the title compound as a yellow solid (0.511 g, 67%).

MS(ESI,neg.ion)m/z:188.1[M-H]^-；

¹H NMR(DMSO-d₆,600MHz)δ(ppm):13.06(s,1H),8.08(s,2H),7.78～7.75(m,2H),7.72～7.68(m,1H),7.60～7.57(m,1H)；

¹³C NMR(DMSO-d₆,151MHz)δ(ppm):167.7,137.5,136.3,131.7,129.6,128.9,128.5,124.4.

Step 2) synthesis of 2- (2H-1,2, 3-triazole-2-yl) benzoyl chloride

The title compound of this step was prepared as described in example 1, step 5, by dissolving 2- (2H-1,2, 3-triazol-2-yl) benzoic acid (0.37g,1.96mmol) in dry dichloromethane (20mL) and slowly adding thionyl chloride (6mL,82.7mmol) and pyridine (0.04mL,0.5 mmol). And gradually heating the reaction solution to reflux, stopping the reaction after reacting for 3 hours, cooling, slowly evaporating the solvent under reduced pressure, and directly entering the next step to obtain the product.

Step 3) (5- (1, 6-naphthyridin-5-yl) hexahydropyrrolo [3, 4-c)]Pyrrol-2 (1H) -yl) (2- (2H-1, synthesis of 2, 3-triazole-2-yl) phenyl) ketone

This step titled compound was prepared by the method described in example 1, step 6, i.e. 5- (hexahydropyrrolo [3,4-c ] pyrrol-2 (1H) -yl-1, 6-naphthyridine (0.30g,1.08mmol), triethylamine (0.33g,3.25mmol) and 2- (2H-1,2, 3-triazol-2-yl) benzoyl chloride (0.34g,1.63mmol) were reacted in dichloromethane (30mL) and the crude product was purified by silica gel column chromatography (petroleum ether/ethyl acetate (v/v) ═ 1/2) to afford the title compound (pale yellow solid, 0.27g, 60.54%).

MS(ESI,pos.ion)m/z:412.45[M+H]⁺；

¹H NMR(CDCl₃,600MHz)δ(ppm):8.90(dd,J＝4.1,1.2Hz,1H),8.44(d,J＝8.5Hz,1H),8.21(d,J＝5.8Hz,1H),7.97(d,J＝8.1Hz,1H),7.80～7.70(m,2H),7.54～7.48(m,1H),7.45～7.39(m,2H),7.31(dd,J＝8.5,4.2Hz,1H),7.30～7.25(m,1H),4.08(dd,J＝10.8,7.5Hz,1H),3.95(dd,J＝10.9,7.1Hz,1H),3.89(dd,J＝12.6,7.6Hz,1H),3.81(dd,J＝10.9,5.3Hz,1H),3.77～3.66(m,2H),3.45～3.35(m,1H),3.12～2.93(m,3H)；

¹³C NMR(CDCl₃,151MHz)δ(ppm):168.2,157.3,153.4,153.0,144.8,136.0,135.8,135.6,134.3,130.1,129.9,128.3,128.0,122.3,119.5,114.9,113.3,51.7,49.7,41.1.

Example 3 Synthesis of (5- (1, 6-naphthyridin-5-yl) hexahydropyrrolo [3,4-c ] pyrrol-2 (1H) -yl) (2-fluoro-6- (2H-1,2, 3-triazol-2-yl) phenyl) methanone

Step 1) synthesis of 2-fluoro-6- (2H-1,2, 3-triazole-2-yl) benzoic acid

The title compound was prepared as described in example 1, step 4 by reacting 2H-1,2, 3-triazole (6.9g,100mmol), 2-fluoro-6-iodobenzoic acid (10.64g,40mmol), cesium carbonate (23.4g,71.7mmol), trans-N, N' -dimethyl-1, 2-cyclohexanediamine (1.02g,7.04mmol) and cuprous iodide (0.76g,4.0mmol) in N, N-dimethylformamide (50mL) and purifying the crude product by silica gel column chromatography (dichloromethane/methanol (v/v) ═ 50/1) to give the title compound as a yellow solid (5.62 g, 67.90%).

MS(ESI,pos.ion)m/z:208.10[M+H]⁺

¹H NMR(DMSO-d₆,400MHz)δ(ppm):13.66(s,1H),8.16(s,2H),7.79(d,J＝8.2Hz,1H),7.68(td,J＝8.2,6.2Hz,1H),7.44(t,J＝8.8Hz,1H).

Step 2) synthesis of 2-fluoro-6- (2H-1,2, 3-triazole-2-yl) benzoyl chloride

The title compound of this step was prepared as described in example 1, step 5, by dissolving 2-fluoro-6- (2H-1,2, 3-triazol-2-yl) benzoic acid (0.69g,3.33mmol) in dry dichloromethane (20mL) and slowly adding thionyl chloride (8mL,109.0mmol) and DMF (0.04mL,0.5 mmol). And gradually heating the reaction solution to reflux, stopping the reaction after reacting for 3 hours, cooling, slowly evaporating the solvent under reduced pressure, and directly entering the next step to obtain the product.

Step 3) (5- (1, 6-naphthyridin-5-yl) hexahydropyrrolo [3, 4-c)]Pyrrole-2 (1H) -yl) (2-fluoro-6- Synthesis of (2H-1,2, 3-triazole-2-yl) phenyl) methanone

The title compound was prepared as described in example 1, step 6 by reacting 5- (hexahydropyrrolo [3,4-c ] pyrrol-2 (1H) -yl-1, 6-naphthyridine (0.30g,1.08mmol), triethylamine (0.33g,3.25mmol) and 2-fluoro-6- (2H-1,2, 3-triazol-2-yl) benzoyl chloride (0.37g,1.63mmol) in dichloromethane (30mL) and the crude product was purified by silica gel column chromatography (petroleum ether/ethyl acetate (v/v) ═ 1/2) to give the title compound (pale yellow dope, 0.34g, 73.06%).

MS(ESI,pos.ion)m/z:430.20[M+H]⁺；

¹H NMR(CDCl₃,600MHz,)δ(ppm):9.00(s,1H),8.79(dd,J＝18.9,8.0Hz,1H),7.89(d,J＝31.9Hz,1H),7.81～7.68(m,3H),7.52(s,1H),7.44(dd,J＝14.1,7.9Hz,1H),7.24(s,1H),7.09(dt,J＝23.4,8.3Hz,1H),4.31(d,J＝46.7Hz,2H),4.12～3.54(m,5H),3.34～3.11(m,3H).

EXAMPLE 4 Synthesis of ethyl 2- ((5- (5- (5-methyl-2- (2H-1,2, 3-triazol-2-yl) benzoyl) hexahydropyrrolo [3,4-c ] pyrrol-2 (1H) -yl) -1, 6-naphthyridin-2-yl) oxy) acetate

Step 1) Synthesis of 5-chloro-1, 6-naphthyridine-1-oxide

5-chloro-1, 6-naphthyridine (11.00g,66.83mmol) was dissolved in dichloromethane (200mL), and m-chloroperoxybenzoic acid (17.30g,100.2mmol) was slowly added thereto at 0 ℃ and the reaction was then switched to room temperature. After completion of the reaction, the reaction mixture was washed with a saturated sodium carbonate solution (200mL), and the separated organic phase was washed successively with water (200mL × 3) and a saturated brine (200mL), followed by drying over anhydrous sodium sulfate, filtration, removal of the solvent by distillation under reduced pressure, and separation and purification by silica gel column chromatography (dichloromethane/methanol (v/v) ═ 100/1) to give the title compound (pale yellow solid, 10.79g, 89.40%).

MS(ESI,pos.ion)m/z:181.15[M+H]⁺；

¹H NMR(DMSO-d₆,400MHz)δ(ppm):8.83(d,J＝6.2Hz,1H),8.56(d,J＝6.0Hz,1H),8.34(d,J＝6.0Hz,1H),8.10(d,J＝8.7Hz,1H),7.70(dd,J＝8.7,6.2Hz,1H).

Step 2)5- (5- (tert-Butoxycarbonyl) hexahydropyrrolo [3,4-c]Pyrrol-2 (1H) -yl) -1, 6-diazepines Synthesis of naphthalene-1-oxide

The title compound was prepared as described in example 1, step 2, i.e. 5-chloro-1, 6-naphthyridine-1-oxide (0.10g,0.55mmol), t-butyl hexahydropyrrolo [3,4-c ] pyrrole-2 (1H) -carboxylate (0.14g,0.66mmol), palladium acetate (0.012g,0.06mmol), 2-dicyclohexyl-phosphorus-2, 4, 6-triisopropylbiphenyl (0.07g,0.11mmol) and sodium carbonate (0.12g,1.11mmol) in toluene (6mL) at 100 ℃ for 24 hours under nitrogen protection and was purified by silica gel column chromatography (dichloromethane/methanol (v/v) ═ 40/1) to give the title compound (yellow solid, 0.13g, 65.87%).

MS(ESI,pos.ion)m/z:357.25[M+H]⁺；

¹H NMR(CDCl₃,400MHz)δ(ppm):8.54(d,J＝6.1Hz,1H),8.26(d,J＝6.0Hz,1H),8.05(d,J＝8.8Hz,1H),7.85(d,J＝6.0Hz,1H),7.20(dd,J＝8.7,6.2Hz,1H),4.09(dd,J＝11.1,7.1Hz,2H),3.77(d,J＝10.2Hz,2H),3.72～3.62(m,2H),3.42(d,J＝9.9Hz,1H),3.38～3.29(m,1H),3.10～2.98(m,2H),1.47(s,9H).

Step 3)5- (2-oxo-1, 2-dihydro-1, 6-naphthyridin-5-yl) hexahydropyrrolo [3, 4-c)]Pyrrole-2 (1H) Synthesis of tert-butyl-formate

5- (5- (tert-Butoxycarbonyl) hexahydropyrrolo [3,4-c ] pyrrol-2 (1H) -yl) -1, 6-naphthyridine-1-oxide (0.50g,1.40mmol), triethylamine (0.42g,4.21mmol) and tetrahydrofuran (20mL) were added to a 100mL reaction flask, trifluoroacetic anhydride (1.79g,8.42mmol) was slowly added dropwise thereto at 0 deg.C, and then the reaction was continued at 0 deg.C for 1.5 hours. The reaction was stopped, the reaction was quenched by addition of methanol (20mL), the solvent was distilled off under reduced pressure, and the solid was washed with saturated sodium bicarbonate solution (100mL) and extracted with dichloromethane (20 mL. times.3). The organic phase was dried over anhydrous sodium sulfate, filtered, and the solvent was distilled off under reduced pressure and then purified by silica gel column chromatography (petroleum ether/ethyl acetate (v/v) ═ 1/1) to give the title compound (pale yellow solid, 0.38g, 76.0%).

MS(ESI,pos,ion)m/z:357.40[M+H]⁺；

¹HNMR(CDCl₃,400MHz)δ(ppm):12.16(s,1H),8.14(d,J＝9.9Hz,1H),8.06(d,J＝5.6Hz,1H),6.69(d,J＝5.6Hz,1H),6.54(d,J＝9.9Hz,1H),3.99(dd,J＝10.7,7.0Hz,2H),3.72～3.67(m,2H),3.66～3.61(m,2H),3.42～3.32(m,2H),3.02～2.96(m,2H),1.47(s,9H).

Step 4)5- (2- (2-ethoxy-2-oxoethoxy) -1, 6-naphthyridin-5-yl) hexahydropyrrolo [3,4- c]Synthesis of pyrrole-2 (1H) -carboxylic acid tert-butyl ester

Tert-butyl 5- (2-oxo-1, 2-dihydro-1, 6-naphthyridin-5-yl) hexahydropyrrolo [3,4-c ] pyrrole-2 (1H) -carboxylate (1.24g,3.48mmol), ethyl 2-bromoacetate (1.74g,10.4mmol), potassium carbonate (1.46g,10.4mmol) and DMF (15mL) were added to a 100mL reaction flask and reacted at room temperature for 12 hours. The reaction was stopped, and the reaction mixture was diluted with water (50mL) and extracted with dichloromethane (50 mL. times.3). The combined organic phases were washed with water (50mL × 2), dried over anhydrous sodium sulfate, filtered, and the solvent was distilled off under reduced pressure and then purified by silica gel column chromatography (petroleum ether/ethyl acetate (v/v) ═ 1/1) to give the title compound (pale yellow dope, 1.10g, 71.4%).

MS(ESI,pos.ion)m/z:443.25[M+H]⁺；

¹H NMR(CDCl₃,400MHz)δ(ppm):8.09(d,J＝6.0Hz,1H),8.03(d,J＝10.0Hz,1H),6.56(d,J＝9.9Hz,1H),6.38(d,J＝6.0Hz,1H),4.99(s,2H),4.22(q,J＝7.1Hz,2H),3.94(dd,J＝10.8,7.1Hz,2H),3.62(d,J＝8.6Hz,4H),3.39～3.25(m,2H),2.95(d,J＝5.1Hz,2H),1.45(s,9H),1.26(t,J＝7.2Hz,3H).

Step 5)2- ((5-hexahydropyrrolo [3, 4-c)]Pyrrole-2 (1H) -1, 6-naphthyridin-2-yl) oxy) acetic acid ethyl ester Synthesis of esters

Tert-butyl 5- (2- (2-ethoxy-2-oxoethoxy) -1, 6-naphthyridin-5-yl) hexahydropyrrolo [3,4-c ] pyrrole-2 (1H) -carboxylate (1.10g,2.49mmol) was dissolved in dichloromethane (10mL), a solution of hydrogen chloride in ethyl acetate (10mL) was added with stirring at room temperature, and the reaction solution was reacted at room temperature for 2 hours. The reaction was stopped, and the solvent was distilled off under reduced pressure to give the title compound (pale yellow solid, 0.93g, 98.8%).

MS(ESI,pos.ion)m/z:343.20[M+H]⁺；

¹H NMR(D₂O,400MHz)δ(ppm):8.43(d,J＝10.2Hz,1H),7.87(d,J＝7.5Hz,1H),7.01(d,J＝7.5Hz,1H),6.75(d,J＝10.2Hz,1H),5.13(s,2H),4.26～4.15(m,4H),3.94(dd,J＝11.1,3.0Hz,2H),3.67(dd,J＝11.4,6.0Hz,2H),3.47～3.30(m,4H),1.20(t,J＝7.1Hz,3H).

Step 6)2- ((5- (5- (5-methyl-2- (2H-1,2, 3-triazole-2-yl) benzoyl) hexahydropyrrolo [3, 4-c]synthesis of pyrrol-2 (1H) -yl) -1, 6-naphthyridin-2-yl) oxy) acetic acid ethyl ester

This step is prepared as described in example 1, step 6, by reacting ethyl 2- ((5-hexahydropyrrolo [3,4-c ] pyrrol-2 (1H) -1, 6-naphthyridin-2-yl) oxy) acetate (0.19g,0.50mmol), triethylamine (0.15g,1.51mmol) and 5-methyl-2- (2H-1,2, 3-triazol-2-yl) benzoyl chloride (0.17g,0.75mmol) in dichloromethane (30mL) and purifying the crude product by silica gel column chromatography (dichloromethane/methanol (v/v) ═ 100/1) to give the title compound (light yellow dope, 0.22g, 83.13%).

MS(ESI,pos.ion)m/z:528.30[M+H]⁺；

¹H NMR(CDCl₃,400MHz)δ(ppm):8.09(d,J＝6.0Hz,1H),7.97(d,J＝9.9Hz,1H),7.81(d,J＝8.3Hz,1H),7.74(d,J＝5.1Hz,2H),7.29(d,J＝6.5Hz,1H),7.21(s,1H),6.54(d,J＝9.9Hz,1H),6.39(d,J＝6.0Hz,1H),4.98(s,2H),4.22(q,J＝7.1Hz,2H),4.00～3.39(m,8H),3.08(q,J＝7.3Hz,2H),2.38(s,3H),1.23(s,3H).

EXAMPLE 5 Synthesis of ethyl 2- ((5- (5- (2- (2H-1,2, 3-triazol-2-yl) benzoyl) hexahydropyrrolo [3,4-c ] pyrrol-2 (1H) -yl) -1, 6-naphthyridin-2-yl) oxy) acetate

This step was prepared by the method described in example 1, step 6, i.e. ethyl 2- ((5-hexahydropyrrolo [3,4-c ] pyrrol-2 (1H) -1, 6-naphthyridin-2-yl) oxy) acetate (0.35g,0.92mmol), triethylamine (0.28g,2.77mmol) and 2- (2H-1,2, 3-triazol-2-yl) benzoyl chloride (0.29g,1.39mmol) were reacted in dichloromethane (30mL) and the crude product was purified by silica gel column chromatography (dichloromethane/methanol (v/v) ═ 100/1) to give the title compound as a pale yellow viscous mass (0.37g, 77.97%).

MS(ESI,pos.ion)m/z:514.30[M+H]⁺；

¹H NMR(CDCl₃,400MHz)δ(ppm):8.12(d,J＝5.9Hz,1H),8.00(d,J＝9.3Hz,2H),7.80(s,2H),7.60～7.49(m,1H),7.44(d,J＝4.3Hz,2H),6.57(d,J＝9.9Hz,1H),6.41(d,J＝5.9Hz,1H),5.02(d,J＝1.7Hz,2H),4.25(q,J＝7.1Hz,2H),3.98(dd,J＝10.9,7.3Hz,1H),3.87(ddd,J＝19.2,11.8,7.4Hz,2H),3.79～3.65(m,2H),3.60(dd,J＝10.9,4.6Hz,1H),3.41(s,1H),3.13～2.89(m,3H),1.29(s,3H).

EXAMPLE 6 Synthesis of ethyl 2- ((5- (5- (2-fluoro-6- (2H-1,2, 3-triazol-2-yl) benzoyl) hexahydropyrrolo [3,4-c ] pyrrol-2 (1H) -yl) -1, 6-naphthyridin-2-yl) oxy) acetate

The title compound was prepared as described in example 1, step 6 by reacting ethyl 2- ((5-hexahydropyrrolo [3,4-c ] pyrrol-2 (1H) -1, 6-naphthyridin-2-yl) oxy) acetate (0.35g,0.92mmol), triethylamine (0.28g,2.77mmol) and 2-fluoro-6- (2H-1,2, 3-triazol-2-yl) benzoyl chloride (0.31g,1.39mmol) in dichloromethane (30mL) and purifying the crude product by silica gel column chromatography (dichloromethane/methanol (v/v) ═ 100/1) to give the title compound as a pale yellow dope, 0.39g, 79.42%).

MS(ESI,pos.ion)m/z:532.30[M+H]⁺；

¹HNMR(CDCl₃,400MHz)δ(ppm):8.13(d,J＝5.9Hz,1H),8.03(q,J＝8.8Hz,1H),7.86(dd,J＝10.9,7.0Hz,1H),7.82(d,J＝5.4Hz,1H),7.82～7.79(m,1H),7.54～7.47(m,1H),7.17(t,J＝8.2Hz,1H),6.68～6.53(m,1H),6.42(dd,J＝14.4,6.0Hz,1H),5.10～4.95(m,2H),4.25(q,J＝7.1Hz,2H),4.06～3.59(m,7H),3.35～3.07(m,3H),1.29(s,3H).

EXAMPLE 7 Synthesis of 2- ((5- (5- (5-methyl-2- (2H-1,2, 3-triazol-2-yl) benzoyl) hexahydropyrrolo [3,4-c ] pyrrol-2 (1H) -yl) -1, 6-naphthyridin-2-yl) oxy) acetic acid

Mixing 2- ((5- (5- (5-methyl-2- (2H-1,2, 3-triazole-2-yl) benzoyl) hexahydropyrrolo [3, 4-c)]Ethyl pyrrol-2 (1H) -yl) -1, 6-naphthyridin-2-yl) oxyacetate (0.50g,0.95mmol) was added to a 100mL single-necked flask, followed by addition of cesium carbonate (0.93g,2.84mmol) and methanol (30mL), and reacted at 60 ℃ overnight. Stopping the reaction, adjusting the pH of the reaction solution to 2.0 by using dilute hydrochloric acid,the solvent was then removed by distillation under the reduced pressure, and the crude product was isolated and purified by silica gel column chromatography (dichloromethane/methanol (v/v) ═ 20/1) to give the title compound (pale yellow solid, 0.38g, 79.96%). MS (ESI, pos. ion) M/z 500.21[ M + H ]]⁺；

¹H NMR(CDCl₃,400MHz)δ(ppm):8.16(d,J＝5.8Hz,1H),7.99(d,J＝9.9Hz,1H),7.81(d,J＝8.5Hz,1H),7.75(s,2H),7.35～7.29(m,1H),6.75～6.59(m,2H),6.54(d,J＝9.9Hz,1H),4.83(s,2H),4.00～3.90(m,1H),3.91～3.79(m,2H),3.73～3.61(m,2H),3.56(dd,J＝10.9,4.5Hz,1H),3.46～3.28(m,1H),3.09～2.84(m,3H),2.43(s,3H).

EXAMPLE 8 Synthesis of 2- ((5- (5- (2- (2H-1,2, 3-triazol-2-yl) benzoyl) hexahydropyrrolo [3,4-c ] pyrrol-2 (1H) -yl) -1, 6-naphthyridin-2-yl) oxy) acetic acid

This step title compound was prepared as described in example 7, step 1, i.e. ethyl 2- ((5- (5- (2- (2H-1,2, 3-triazol-2-yl) benzoyl) hexahydropyrrolo [3,4-c ] pyrrol-2 (1H) -yl) -1, 6-naphthyridin-2-yl) oxy) acetate (0.50g,0.97mmol) and cesium carbonate (0.95g,2.92mmol) were reacted in methanol (30mL) at 60 ℃ and the crude product was purified by silica gel column chromatography (dichloromethane/methanol (v/v) ═ 20/1) to give the title compound as a pale yellow solid (0.36 g, 75.68%).

MS(ESI,pos.ion)m/z:486.19[M+H]⁺；

¹H NMR(CDCl₃,400MHz)δ(ppm):8.12(d,J＝5.9Hz,1H),7.99(d,J＝9.7Hz,1H),7.80(d,J＝8.5Hz,1H),7.77(s,2H),7.31～7.26(m,1H),6.73～6.59(m,2H),6.54(d,J＝9.8Hz,1H),4.85(s,2H),4.01～3.97(m,1H),3.91～3.77(m,2H),3.73～3.61(m,2H),3.54(dd,J＝10.9,4.5Hz,1H),3.46～3.27(m,1H),3.09～2.83(m,3H).

EXAMPLE 9 Synthesis of 2- ((5- (5- (2-fluoro-6- (2H-1,2, 3-triazol-2-yl) benzoyl) hexahydropyrrolo [3,4-c ] pyrrol-2 (1H) -yl) -1, 6-naphthyridin-2-yl) oxy) acetic acid

This step was prepared by the method described in example 7, step 1, i.e. ethyl 2- ((5- (5- (2-fluoro-6- (2H-1,2, 3-triazol-2-yl) benzoyl) hexahydropyrrolo [3,4-c ] pyrrol-2 (1H) -yl) -1, 6-naphthyridin-2-yl) oxy) acetate (0.50g,0.94mmol) and cesium carbonate (0.92g,2.82mmol) were reacted in methanol (30mL) at 60 ℃ and the crude product was purified by silica gel column chromatography (dichloromethane/methanol (v/v) ═ 20/1) to give the title compound as a pale yellow solid (0.38g, 80.1%).

MS(ESI,pos.ion)m/z:504.18[M+H]⁺；

¹H NMR(CDCl₃,400MHz)δ(ppm):8.13(d,J＝5.8Hz,1H),7.97(d,J＝10.0Hz,1H),7.83(d,J＝8.7Hz,1H),7.73(s,2H),7.36～7.29(m,1H),6.77～6.57(m,2H),4.81(s,2H),4.03～3.90(m,1H),3.93～3.79(m,2H),3.71～3.61(m,2H),3.54(dd,J＝10.7,4.5Hz,1H),3.45～3.28(m,1H),3.09～2.87(m,3H).

EXAMPLE 10 Synthesis of 2- ((5- (5- (5-methyl-2- (2H-1,2, 3-triazol-2-yl) benzoyl) hexahydropyrrolo [3,4-c ] pyrrol-2 (1H) -yl) -1, 6-naphthyridin-2-yl) oxy) acetamide

Step 1)5- (2- (2-amino-2-oxoethoxy) -1, 6-naphthyridin-5-yl) hexahydropyrrolo [3, 4-c)] Synthesis of pyrrole-2 (1H) -carboxylic acid tert-butyl ester

Tert-butyl 5- (2- (2-ethoxy-2-oxoethoxy) -1, 6-naphthyridin-5-yl) hexahydropyrrolo [3,4-c ] pyrrole-2 (1H) -carboxylate (0.50g,1.17mmol) was added to a 100mL reaction flask, followed by addition of a methanol solution of ammonia (20mL), the reaction was stopped after the reaction solution was stirred for 72 hours at room temperature, the solvent was removed by distillation under the reduced pressure, and the crude product was isolated and purified by silica gel column chromatography (dichloromethane/methanol (v/v) ═ 50/1) to give the title compound (pale yellow solid, 0.44g, 92.12%).

MS(ESI,pos.ion)m/z:414.23[M+H]⁺；

¹H NMR(CDCl₃,400MHz)δ(ppm):8.10(d,J＝5.8Hz,1H),8.01(d,J＝9.9Hz,1H),6.58(d,J＝9.7Hz,1H),6.34(d,J＝6.0Hz,1H),5.01(s,2H),3.92(dd,J＝10.7,7.2Hz,2H),3.63(d,J＝8.6Hz,4H),3.39～3.27(m,2H),2.95(d,J＝5.1Hz,2H),1.43(s,9H).

Step 2)2- ((5- (hexahydropyrrolo [3, 4-c)]Pyrrol-2 (1H) -yl) -1, 6-naphthyridin-2-yl) oxy) Synthesis of acetamide

Tert-butyl 5- (2- (2-amino-2-oxoethoxy) -1, 6-naphthyridin-5-yl) hexahydropyrrolo [3,4-c ] pyrrole-2 (1H) -carboxylate (1.00g,2.42mmol) was dissolved in dichloromethane (10mL), a solution of hydrogen chloride in ethyl acetate (10mL) was added with stirring at room temperature, and the reaction solution was reacted at room temperature for 2 hours. The reaction was stopped and the solvent was distilled off under reduced pressure to give the title compound (pale yellow solid, 0.95g, 95.3%).

MS(ESI,pos.ion)m/z:314.16[M+H]⁺；

¹H NMR(DMSO-d₆,400MHz)δ(ppm):8.41(d,J＝10.3Hz,1H),7.88(d,J＝7.5Hz,1H),7.02(d,J＝7.5Hz,1H),6.69(d,J＝10.2Hz,1H),4.63(s,2H),4.26～4.17(m,4H),3.69(dd,J＝11.4,6.0Hz,2H),3.49～3.35(m,4H).

Step 3)2- ((5- (5- (5-methyl-2- (2H-1,2, 3-triazol-2-yl) benzoyl (hexahydropyrrolo [3, 4-c]synthesis of pyrrol-2 (1H) -yl) -1, 6-naphthyridin-2-yl) oxy) acetamide

This step is prepared as described in example 1, step 6, by reacting 2- ((5-hexahydropyrrolo [3,4-c ] pyrrol-2 (1H) -1, 6-naphthyridin-2-yl) oxy) acetamide (0.50g,1.60mmol), triethylamine (0.48g,4.80mmol) and 5-methyl-2- (2H-1,2, 3-triazol-2-yl) benzoyl chloride (0.53g,2.39mmol) in dichloromethane (30mL) and purifying the crude product by silica gel column chromatography (dichloromethane/methanol (v/v) ═ 20/1) to give the title compound (pale yellow solid, 0.66g, 82.56%).

MS(ESI,pos.ion)m/z:499.40[M+H]⁺；

¹H NMR(CDCl₃,400MHz)δ(ppm):8.12(d,J＝5.9Hz,1H),8.00(d,J＝9.9Hz,1H),7.83(d,J＝8.3Hz,1H),7.76(s,2H),7.36～7.27(m,1H),7.22(s,1H),6.77～6.59(m,2H),6.55(d,J＝9.9Hz,1H),5.90(s,1H),4.87(s,2H),4.02～3.90(m,1H),3.91～3.77(m,2H),3.73～3.62(m,2H),3.56(dd,J＝10.9,4.5Hz,1H),3.48～3.28(m,1H),3.07～2.84(m,3H),2.41(s,3H)；

¹³C NMR(CDCl₃,150MHz)δ(ppm):169.4,168.4,162.0,157.7,148.5,147.5,138.6,137.1,135.8,133.6,130.7,129.8,128.3,122.2,117.3,104.2,101.2,51.6,46.5,46.0,41.0,21.0.

EXAMPLE 11 Synthesis of 2- ((5- (5- (2- (2H-1,2, 3-triazol-2-yl) benzoyl) hexahydropyrrolo [3,4-c ] pyrrol-2 (1H) -yl) -1, 6-naphthyridin-2-yl) oxy) acetamide

This step was prepared by the method described in example 1, step 6, i.e. 2- ((5-hexahydropyrrolo [3,4-c ] pyrrol-2 (1H) -1, 6-naphthyridin-2-yl) oxy) acetamide (0.45g,1.44mmol), triethylamine (0.44g,4.31mmol) and 2- (2H-1,2, 3-triazol-2-yl) benzoyl chloride (0.45g,2.15mmol) were reacted in dichloromethane (30mL) and the crude product was purified by silica gel column chromatography (dichloromethane/methanol (v/v) ═ 20/1) to give the title compound (pale yellow solid, 0.57g, 82.63%).

MS(ESI,pos.ion)m/z:485.10[M+H]⁺；

¹H NMR(CDCl₃,400MHz)δ(ppm):8.13(d,J＝5.9Hz,1H),7.99(t,J＝9.2Hz,2H),7.79(s,2H),7.59～7.48(m,1H),7.44(t,J＝6.3Hz,2H),6.72(d,J＝5.9Hz,1H),6.55(d,J＝9.9Hz,2H),5.87(s,1H),4.86(s,2H),3.96(dd,J＝10.9,7.3Hz,1H),3.93～3.77(m,2H),3.69(dd,J＝11.7,4.7Hz,2H),3.59(dd,J＝10.9,4.6Hz,1H),3.48～3.28(m,1H),3.05(d,J＝7.3Hz,2H),2.94(d,J＝5.9Hz,1H)；

¹³C NMR(CDCl₃,100MHz)δ(ppm):169.5,168.3,162.1,157.9,148.7,147.6,137.2,136.2,135.9,130.2,130.1,128.4,128.1,122.4,117.4,104.4,101.4,54.7,51.8,49.7,41.2.

EXAMPLE 12 Synthesis of 2- ((5- (5- (2-fluoro-6- (2H-1,2, 3-triazol-2-yl) benzoyl) hexahydropyrrolo [3,4-c ] pyrrol-2 (1H) -yl) -1, 6-naphthyridin-2-yl) oxy) acetamide

This step is prepared as described in example 1, step 6, by reacting 2- ((5-hexahydropyrrolo [3,4-c ] pyrrol-2 (1H) -1, 6-naphthyridin-2-yl) oxy) acetamide (0.40g,1.28mmol), triethylamine (0.39g,3.83mmol) and 2-fluoro-6- (2H-1,2, 3-triazol-2-yl) benzoyl chloride (0.43g,1.91mmol) in dichloromethane (30mL) and purifying the crude product by silica gel column chromatography (dichloromethane/methanol (v/v) ═ 20/1) to give the title compound (pale yellow solid, 0.52g, 81.75%).

MS(ESI,pos.ion)m/z:503.21[M+H]⁺；

¹H NMR(CDCl₃,400MHz)δ(ppm):8.13(dd,J＝5.7,3.5Hz,1H),8.03(t,J＝9.2Hz,1H),7.96～7.64(m,3H),7.49(tt,J＝12.1,6.0Hz,1H),7.16(t,J＝8.4Hz,1H),6.72(dd,J＝13.0,5.9Hz,1H),6.56(dd,J＝18.2,9.9Hz,2H),5.90(s,1H),4.96～4.76(m,2H),4.09～3.83(m,3H),3.82～3.51(m,4H),3.29(dd,J＝10.5,3.7Hz,1H),3.19～2.95(m,2H).

Biological assay

₁EXAMPLE A antagonism of humanized OX receptors by Compounds of the invention

Test method

Evaluation of the Effect of Compounds of the invention on agonist-induced cellular calcium flux Using fluorometric assays to assess the Effect of Compounds of the invention on humanized OX expressed on Chinese hamster ovary Cells (CHO)₁Antagonistic ability of the receptor. Suspending the cells in DMEM cultureIn nutrient medium (invitrogen), then at 2X 10⁴The density of cells/wells is distributed in the microwell reaction plate. Hank's balanced salt solution (HBSS, Invitrogen) (pH 7.4) containing fluorescent probe (Fluo4NW, Invitrogen), probenecid, and 20mM hydroxyethylpiperazine ethanethiosulfonic acid (Invitrogen) was added to the above microwell reaction plate, followed by incubation with cells at 37 ℃ for 60min and 22 ℃ for 15 min. The reaction plates were placed in a cytofluorimetric workstation (CellLux, PerkinElmer) and the test compound or reference antagonist or Hank balanced salt solution was added 5min later with 3nM orexin a or Hank balanced salt buffer (blank control) and the change in fluorescence intensity was measured, which was positively correlated to the change in intracellular free calcium ion concentration. The results are expressed as percent orexin a inhibition relative to the control group at 3 nM.

IC was calculated by obtaining dose-response curves through experimental testing of serial concentrations with the standard reference antagonist being SB334867₅₀The value is obtained.

Experimental results see Table 1, Table 1 for compound pairs of OX as provided in some examples of the invention₁Results of receptor antagonism experiments.

TABLE 1 Compound pairs OX as provided in the examples of the invention₁Results of receptor antagonism experiments

The experimental results show that the compound of the invention is OX₁The receptor shows better antagonism.

₂EXAMPLE B antagonism of humanized OX receptors by Compounds of the invention

Test method

Evaluation of the Effect of Compounds of the invention on agonist-induced cellular calcium flux Using fluorometry to detect the Effect of Compounds of the invention on humanized OX expressed on HEK-293 cells₂Antagonistic ability of the receptor. Cells were suspended in DMEM medium (invitrogen) and then plated at 3X 10⁴Cell/pore density distributionIn a microwell reaction plate. Hank's balanced salt buffer (HBSS, Invitrogen) (pH 7.4) containing fluorescent probe (Fluo4NW, Invitrogen), probenecid, and 20mM hydroxyethylpiperazine ethiosulfonic acid was added to the microwell reaction plate, followed by incubation with the cells at 37 ℃ for 60min and 22 ℃ for 15 min. The reaction plates were placed in a cytofluorimetric workstation (CellLux, PerkinElmer) and the test compound or reference antagonist or Hank balanced salt solution was added 5min later with 10nM orexin B or Hank balanced salt buffer (blank control) and the change in fluorescence intensity was measured, which was positively correlated to the change in intracellular free calcium ion concentration. The results are expressed as the percentage inhibition of orexin B at 10nM relative to the control group.

The standard reference antagonist is JNJ10397049, and an amount effect curve is obtained through the experimental test of a series of concentrations, so that the IC is calculated₅₀The value is obtained.

Experimental results see Table 2, Table 2 providing Compound pairs OX as part of the examples of the invention₂Results of receptor antagonism experiments.

TABLE 2 Compound pairs OX as provided in the examples of the invention₂Results of receptor antagonism experiments

The experimental results show that the compound of the invention is OX₂The receptor shows better antagonism.

Example C pharmacokinetic evaluation of the Compounds of the invention following intravenous injection or gavage in rats, dogs and monkeys

The present invention evaluates the pharmacokinetic studies of the compounds of the invention in rats, dogs and monkeys, with the animal information detailed in table a.

Table a information sheet of the subject animals of the present invention

Test method

The compounds of the invention were administered to the test animals as 5% DMSO + 5% Kolliphor HS 15+ 2% (2% HCl) + 88% Saline solution or 10% DMSO + 10% Kolliphor HS 15+ 80% physiological Saline solution. For the group administered by intravenous injection, the dose was 1mg/kg or 2mg/kg, followed by intravenous blood (0.3mL) at time points of 0.083, 0.25, 0.5, 1.0, 2.0, 4.0, 6.0, 8.0 and 24 hours after administration and centrifugation at 3,000 or 4,000rpm for 10 minutes, and the plasma solution was collected and stored at-20 ℃ or-70 ℃. For the gavage administration group, the dose was 2.5mg/kg or 5mg/kg, and then blood was taken intravenously (0.3mL) at time points of 0.25, 0.5, 1.0, 2.0, 4.0, 6.0, 8.0, and 24 hours after administration and centrifuged at 3,000 or 4,000rpm for 10 minutes, and the plasma solution was collected and stored at-20 ℃ or-70 ℃. The positive control was suvorexant.

The plasma solutions collected from the above groups were subjected to LC-MS/MS analysis. Analysis results show that the compound has good pharmacokinetic properties of large exposure value, low clearance rate, high bioavailability and the like. The compound of the invention has better drugability and better clinical application prospect.

In the description herein, references to the description of the term "one embodiment," "some embodiments," "an example," "a specific example" or "some examples" or the like are intended to mean that a particular feature, structure, material, or characteristic described in connection with the embodiment or example is included in at least one embodiment or example of the invention. In this specification, the schematic representations of the terms used above are not necessarily intended to refer to the same embodiment or example. Furthermore, the particular features, structures, materials, or characteristics described may be combined in any suitable manner in any one or more embodiments or examples. Furthermore, various embodiments or examples and features of different embodiments or examples described in this specification can be combined and combined by one skilled in the art without contradiction.

Although embodiments of the present invention have been shown and described above, it is understood that the above embodiments are exemplary and should not be construed as limiting the present invention, and that variations, modifications, substitutions and alterations can be made to the above embodiments by those of ordinary skill in the art within the scope of the present invention.

Claims (11)

1. A compound which is a compound represented by formula (II) or a pharmaceutically acceptable salt of a compound represented by formula (II),

wherein:

R¹is H, D, -O- (CH)₂)_n-C(＝O)O-(C_1-6Alkyl), -O- (CH)₂)_n-COOH or-O- (CH)₂)_n-C(＝O)NH₂；

R²、R³、R⁴And R⁵Each independently is H or D;

R⁶and R⁷Each independently is H, D, F, Cl, Br, I, C_1-6Alkyl radical, C_1-6Haloalkyl, C_1-6Alkoxy or C_1-6A haloalkoxy group;

R⁸and R⁹Each independently is H or D; and

each n is independently 1,2,3 or 4.

2. The compound of claim 1, wherein R¹Is H, D, -O- (CH)₂)_n-C(＝O)O-(C_1-4Alkyl), -O- (CH)₂)_n-COOH or-O- (CH)₂)_n-C(＝O)NH₂。

3. The compound of claim 1, wherein R⁶And R⁷Each independently is H, D, F, Cl, Br, I, C_1-4Alkyl radical, C_1-4Haloalkyl, C_1-4Alkoxy or C_1-4A haloalkoxy group.

4. The compound of claim 1, wherein R¹Is H, D, -O-CH₂-C(＝O)O-CH₃、-O-(CH₂)₂-C(＝O)O-CH₃、-O-CH₂-C(＝O)O-CH₂CH₃、-O-(CH₂)₂-C(＝O)O-CH₂CH₃、-O-CH₂-C(＝O)O-CH₂CH₂CH₃、-O-(CH₂)₂-C(＝O)O-CH₂CH₂CH₃、-O-CH₂-C(＝O)O-CH(CH₃)₂、-O-(CH₂)₂-C(＝O)O-CH(CH₃)₂、-O-CH₂-COOH、-O-(CH₂)₂-COOH、-O-CH₂-C(＝O)NH₂or-O- (CH)₂)₂-C(＝O)NH₂。

5. The compound of claim 1, wherein R⁶And R⁷Each independently is H, D, F, Cl, Br, I, methyl, ethyl, n-propyl, isopropyl, -CF₃、-CH₂CF₃、-CF₂CF₃Methoxy, ethoxy, n-propyloxy or isopropyloxy.

6. The compound of claim 1, which is a compound having one of the following structures or a pharmaceutically acceptable salt of a compound having one of the following structures,

7. a pharmaceutical composition comprising a compound of any one of claims 1-6; and

the pharmaceutical composition optionally comprises a pharmaceutically acceptable carrier, excipient, adjuvant, or any combination thereof.

8. Use of a compound according to any one of claims 1 to 6 or a pharmaceutical composition according to claim 7 in the manufacture of a medicament for the prevention, treatment or alleviation of a disease or a disorder associated with the orexin receptor.

9. The use according to claim 8, wherein the orexin receptor-related disease is a sleep disorder, depression, anxiety disorder, panic disorder, obsessive compulsive disorder, affective neuropathy, depressive neuropathy, anxiety neuropathy, mood disorder, panic attack disorder, behavioral disorders, mood disorder, post-traumatic stress disorder, sexual dysfunction, schizophrenia, delirium, dementia, addiction, cognitive disorder, Parkinson's disease, movement disorder, eating disorder, pain, digestive system disease, epilepsy, cardiovascular disease, metabolic disease or immune-related disease.

10. The use according to claim 9, wherein the depression is manic depression; the addiction is a drug dependence; the pain is headache; the cardiovascular disease is hypertension; the immune-related disorder is inflammation; the metabolic disease is diabetes; the dementia is Alzheimer's disease.

11. The use of claim 10, wherein the headache is migraine.